1VATI
       WATER POLLUTION CONTROL RESEARCH SERIES • 16100 EXH 11/71
       INTERNATIONAL SYMPOSIUM
                 ON
       WATER POLLUTION CONTROL
                 IN
          COLD CLIMATES
ENVIRONMENTAL PROTECTION AGENCY0RESEARCH AND MONITORING

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                   International Symposium on

WATER POLLUTION CONTROL
                        IN

            COLD CLIMATES
                  held at the University of Alaska
                      July 22-24, 1970
                       Sponsored by


               INSTITUTE OF WATER RESOURCES
                   UNIVERSITY OF ALASKA

                          and

            FEDERAL WATER QUALITY ADMINISTRATION
                        EDITORS
         R. Sage Murphy                 David Nyquist
        Director, Institute of               Assistant Professor of
         Water Resources                 Water Resources


                    TECHNICAL EDITOR
                       Paul W. Neil
            For sale by the Superintendent of Documents, U.S. Government Printing Office
                  Washington, D.C. 20402 - Price $2.60 (paper cover)
                        Stock Number £501-0208

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                                   INTRODUCTION

The first plans for this symposium were begun by the senior editor during the winter of 1967.
Alaska was  about to become the focal point  for petroleum  interests as a consequence of the
enormous oil discoveries made by the Atlantic-Richfieid and Humble Oil joint venture at Prudhoe
Bay. Coincident with an economic boom in  this sparsely-settled region, federal, state, and private
organizations  instituted more stringent water  pollution control  criteria. The combined events
created an apparent technology gap relative  to water pollution  control in cold climates. The
engineering  and scientific bases for waste treatment and receiving stream  criteria were almost
exclusively dependent upon  temperate experiences. Scattered journal articles about the  North
were  in  evidence, but the majority seemed  repetitious and contributed  little toward a  true
understanding of the problems involved.

It became obvious that more experience in northern applications was available in the circumpolar
countries  than in the temperate areas of the United States.  A symposium of international scope
was therefore envisioned, with representatives  of all the circumpolar nations presenting papers.
With the exception of the Soviet Union and Iceland, all countries participated. The eighteen papers
and two reviews in this volume were selected  from approximately sixty invited abstracts.

Persons living or interested  in the  Far North  need no  statistics to convince them of the area's
potential. It is  not  the purpose of this  introduction to expound on the virtues  of the North;
however, it is our firm belief that the Arctic and sub-Arctic  will be focal points for economic and
resource development, and for available  open  space for the rest of the world in the imminent
future. Some implications of this have already become manifest.

Should such development  indeed  occur,  it would certainly be imperative that workers  in the
circumpolar countries become entirely familiar with the work done in each.

Therefore, besides descriptions of engineered works and scientific studies, the meeting permitted
many the opportunity to personally meet their international counterparts. Since such contact is
often  more important in the long run than the  formal papers, hopefully a continuing exchange of
information between the various groups concerned with water pollution control will evolve.

The first meeting of  such a group is usually difficult. A wide  range of disciplines and organizations
were involved. The most advanced  waste  treatment technology is of no use unless the limits of
materials able to be  discharged into the  receiving waters are  understood; consequently, invited
papers were evenly split between "waste treatment technology" and "effects of wastes upon Far
Northern receiving waters." Thus, an attempt was made to create an atmosphere where engineers
and biologists could  communicate.  In  this endeavor partial  success was achieved. If subsequent
meetings are held in  the future, it is anticipated that they will be devoted to single, more specific
topics  than was our general convocation. Indications are  that such groups will  be meeting in
Alaska, Canada, and Scandanavia in the very near future.

The success of any meeting depends upon a large number of people. We thank the authors  for their
thoughtful manuscript preparation. The secretarial staff and graduate research assistants of the
University of Alaska's Institute of Water Resources unselfishly devoted many hours handling the
thankless  details both in preparation for, and during, the symposium. The banquet talk, which is
not included  in these  papers, was given  by Mr.  Geoffrey Larminie, area manager for British
                                             i ii

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Petroleum (BP Alaska,  Inc.). His talk about the Prudhoe Bay oil fields, how they will be and are
being managed, and the implications concerning water pollution control will be remembered by all
in attendance.

No  meeting is successful without financial backing. The majority of funds for the symposium were
provided by the Federal Water Quality Administration, U. S. Department of the Interior (now the
Environmental  Protection Agency), through grant number 16100 E X H. We are particularly
indebted to Mr. Richard Latimer, Director of FWQA's Alaska  Water Laboratory, and Mr. William
Caw ley of FWQA's Washington, D. C. staff, for their efforts in making the meeting a success. The
Office of Water Resources  Research, U. S. Department of the Interior, and the State of Alaska,
through  their funding of  our Institute,  contributed  significantly,  though indirectly, to this
meeting.  Without their support the symposium could not have been attempted.

The editors sincerely hope this volume will help to bring together some of the existing practices
and theories concerned with water pollution control in cold climates.
                                              R. Sage Murphy

                                              David Nyquist
                                            IV

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                             ACKNOWLEDGMENT

In appreciation of financial contributions without which the Symposium could not have been
convened.

                             Atlantic Richfield Company

                               BP Alaska, Incorporated

                           Humble Oil & Refining Company

                               Marathon Oil Company

                                Texaco. Incorporated

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                             TABLE OF  CONTENTS
                               RECEIVING WATERS

SYNOPTIC STUDY OF ACCELERATED EUTROPHICATION IN LAKE
TAHOE - AN ALPINE LAKE	1

    Charles R. Goldman, Professor of Zoology, Institute of Ecology. University
    of California, Davis, California, U.S.A.

    Gerald Moshiri,  Institute of Ecology,  University  of  California, Oavis,
    California, U.S.A.

    Evelyne de Amezaga, Institute of Ecology, University of California, Davis,
    California, U.S.A.

THE SOUTH BASIN OF LAKE WINNIPEG • AN ASSESSMENT OF POLLUTION  	22

    Jo-Anne M. E. Crowe, Pollution  Biologist, Fisheries Branch, Department of
    Mines and Natural Resources, Winnipeg, Manitoba, Canada

EUTROPHICATION IN SOME LAKES AND COASTAL AREAS IN FINLAND,
WITH SPECIAL REFERENCE TO POLYHUMIC LAKES	„	48

    Pasi  O.  Lehmusluoto,  Assistant  in  the  Department  of  Limnology,
    University of Helsinki, Helsinki, Finland

THE RECOVERY PROCESS OF A LAKE WHICH RECEIVED WASTEWATER
FROM AN ORE DRESSING PLANT	61

    Bengt  Ahling, Research  Engineer, Swedish Water and  Air Pollution
    Research Laboratory. Stockholm, Sweden

DEPLETION OF OXYGEN BY MICROORGANISMS IN ALASKAN RIVERS
AT LOW TEMPERATURES    	71

    Ronald  C.  Gordon, Research Microbiologist, Alaska Water Laboratory,
    Federal Water Pollution Control Administration, College, Alaska, U.S.A.

PREDICTION OF DISSOLVED OXYGEN LEVELS IN THE SOUTH
SASKATCHEWAN RTVER IN WINTER    	96

    Robert C. Landine, Assistant Professor,  Department of Civil Engineering,
    University of New Brunswick, Fredericton, New Brunswick, Canada
                                        VI I

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POLLUTION - A BIOLOGICAL STUDY OF SOME RECEIVING WATERS IN HOKKAIDO   	113

     Matsunae Tsuda, Professor of Zoology, Zoological Institute, Nara Women's
     University, Nara, Japan

     Toshiharu Watanabe, Zoological Institute. Nara Women's University, Nara,
     Japan

     Kozo Tani, Zoological Institute, Nara Women's University, Nara, Japan

CHEMICAL EFFECTS OF SALMON DECOMPOSITION ON AQUATIC ECOSYSTEMS	125

     David  C. Bricked, Graduate  Research  Assistant,  Institute of Marine
     Sciences, University of Alaska, College, Alaska, U.S.A.

     John J. Goering, Professor of Marine Sciences,  Institute of Marine Sciences,
     University of Alaska, College, Alaska, U.S.A.

PHOSPHORUS BINDING MECHANISMS DURING SELF-PURIFICATION OF
POLLUTED LAKES	139

     Jan Werner,  Research Chemist, Swedish Water and Air Pollution Research
     Laboratories, Stockholm, Sweden

CRITICAL REVIEW OF PAPERS ON RECEIVING WATERS   	153

     Peter A. Krenkel, Chairman and Professor, Department of Environmental
     and  Water  Resources  Engineering,  Vanderbilt  University,  Nashville,
     Tennessee, U.S.A.
                              TREATMENT PROCESSES
THE INFLUENCE OF TEMPERATURE ON THE REACTIONS OF THE
ACTIVATED SLUDGE PROCESS	164

     Pal Benedek, Head of Water Quality and Technology Department, Research
     Institute for Water Resources Development, Budapest, Hungary

     Peter Farkas, Senior Research  Biologist, Department of Water Quality and
     Technology,   Research  Institute  for  Water  Resources  Development,
     Budapest, Hungary
                                         VI I I

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TEMPERATURE EFFECTS ON BIOLOGICAL WASTE TREATMENT PROCESSES   	180

    W. Wesley  Eckenfelder,  Jr., Professor  of  Environmental and  Water
    Resources Engineering, Vanderbilt University, Nashville, Tennessee, U.S.A.

    Andrew J. Englande, Jr., Research Assistant, Department of Environmental
    and  Water   Resources  Engineering,  Vanderbilt  University,  Nashville,
    Tennessee, U.S.A.

EVALUATION OF AERATED LAGOONS AS A SEWAGE TREATMENT
FACILITY IN THE CANADIAN PRAIRIE PROVINCES  	191

    Archie  R. Pick, Research Engineer,  Water Works  and Waste Disposal
    Division,  The Metropolitan Corporation of Greater Winnipeg,  Winnipeg,
    Manitoba, Canada

    George E. Burns, Engineer of Design, Water Works and Waste Disposal
    Division,  The Metropolitan Corporation of Greater Winnipeg,  Winnipeg,
    Manitoba, Canada

    Dick  W.  Van Es, Engineer of Sewage Disposal, Water Works and Waste
    Disposal  Division, The Metropolitan  Corporation of Greater  Winnipeg,
    Winnipeg, Manitoba, Canada

    Richard M. Girling,  Assistant  Engineer of Design,  Water Works  and Waste
    Disposal  Division, The Metropolitan  Corporation of Greater  Winnipeg,
    Winnipeg, Manitoba, Canada

DESIGN CONSIDERATIONS FOR EXTENDED AERATION IN ALASKA   	213

    Sidney  E. Clark, Acting Chief,  Cold  Climate  Research  Program, Alaska
    Water Laboratory, Federal Water  Quality Administration, College, Alaska,
    U.S.A.

    Harold  J. Coutts,  Research  Engineer, Cold Climate  Research Program,
    Alaska Water  Laboratory, Federal Water Quality Administration, College,
    Alaska. U.S.A.

    Conrad Christiansen, Research Engineer, Cold Climate Research Program,
    Alaska Water  Laboratory, Federal Water Quality Administration, College,
    Alaska, U.S.A.

CHEMICAL TREATMENT OF MECHANICALLY AND BIOLOGICALLY
TREATED  WASTEWATER	237

    Arne  Rosendahl,  Sanitary   Engineer, Norwegian  Institute  for  Water
     Research, Oslo, Norway
                                           IX

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BIOLOGICAL AND CHEMICAL WASTE TREATMENT EXPERIMENTS IN
FAR NORTHERN SWEDEN  	252

     Peter  Balmer,  Consulting  Engineer,  Allmanna  Ingenjorsbyran  AB,
    Stockholm, Sweden


BIOLOGICAL SEWAGE TREATMENT IN A COLD CLIMATE AREA   	263

     Keichi Koyama, Associate Professor, Department of Sanitary Engineering,
     Hokkaido University. Sapporo, Japan

     Shigeo  Terashima,  Professor,  Department  of  Sanitary  Engineering,
     Hokkaido University, Sapporo, Japan

     Yasumoto  Magara, Instructor,  Department of  Sanitary  Engineering,
     Hokkaido University, Sapporo, Japan

MICROBIOLOGIC INDICATORS OF THE EFFICIENCY OF AN AERATED,
CONTINUOUS-DISCHARGE, SEWAGE LAGOON IN NORTHERN CLIMATES  	286

    John W. Vennes. Professor of Microbiology, School of Medicine. University
    of North Dakota, Grand Forks, North Dakota, U.S.A.

    Otmar 0. Olson, School of Medicine,  University of North Dakota, Grand
     Forks. North Dakota, U.S.A.

DISINFECTION AND TEMPERATURE INFLUENCES	312

    Cecil Chambers, Research Microbiologist,  Biological Research Program,
    Advanced  Waste Treatment  Research, Federal  Water Pollution Control
    Administration, Cincinnati, Ohio, U.S.A.

    Gerald Berg. Chief, Virology Section, Waste Identification and Analyses
    Activities, Advanced Waste Treatment Research, Federal Water Pollution
    Control Administration, Cincinnati. Ohio, U.S.A.

CRITICAL REVIEW OF PAPERS ON TREATMENT PROCESSES	329

     Karl Wuhrmann, Professor, Swiss Federal Institute of Technology, Zurich,
    Switzerland

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          SYNOPTIC  STUDY OF  ACCELERATED  EUTROPHICATION
                      IN  LAKE TAHOE-AN ALPINE  LAKE
                            Charles R. Goldman, Gerald Moshiri
                                 and Evelyne de Amezaga
                                   INTRODUCTION

 Lake Tahoe, located at an elevation of 6,229 feet near the crest of the Sierra-Nevada in a graben
 basin,  is among the clearest alpine lakes in the world. Secchi measurements over 35 meters have
 been recorded and the lake still has an extinction coefficient between 0.047  and 0.061 rn"1. Its
 watershed of 800 Km2 is small in comparison to its surface of 499 Km2. The average depth of
 Tahoe  is 313 meters and it contains 156 Km3 of water with a retention time of about 700 years
 (Fig. 1).

 With the exception  of the  early  observations of  Le Conte  (1883a,  1883b, 1884) and the
 limnological reconnaissance of Juday (1907), Kemmerer et al. (1923), and Hutchinson (1937), the
 lake  has  received little limnological study until the last ten years. Geological  studies of the lake
 have included fathometry of the basin as well as studies of sediment distribution (Court, Goldman,
 and Hyne, in press). The general trophic state  of Tahoe may be classified as very oligotrophic as
 compared with a variety of other lake types (Goldman, 1967, 1968). Attached aquatic plants are
found  to a depth of  100  meters  (Frantz and Cordone,  1967)  and the  crayfish Pacifasticus
leniusculus is extremely abundant in the littoral zone (Abrahamsson and Goldman, 1970).
                                                 .av« Rock
                                Uppw Truckw River
                         FIGURE 1  Lake Tahoe, California-Nevada

                                           1

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Culture experiments show that the  lake is deficient in available iron, that the interaction between
nitrogen and phosphorus in Tahoe is very complicated, and that the various tributaries of the lake
differ greatly in their stimulation of  algal growth (Goldman, 1964; Goldman and Armstrong, 1969;
Goldman, Tunzi, and Armstrong, 1969).

The variation in productivity in the  lake was first documented during two synoptic studies in 1962
(Goldman and Carter, 1965). A second series of three synoptics was run in  1967, and a third series
in 1968 which are reported here.

During the last decade the Tahoe basin, an important recreational area of the Sierra-Nevada, has
undergone a very rapid increase in both resident and visitor population, and despite its great
volume of low nutrient concentration, the measured increase in primary productivity is already a
clear sign of accelerated  eutrophication  (Goldman and Armstrong,  1969). The senior  author
believes that if transparency is reduced by inorganic turbidity or increased  algal growth a lowering
of the lake's heat budget will  occur with  the possibility of freezing. This  hypothesis is currently
under  investigation  since Tahoe does not freeze,  and  a winter ice  cover, by promoting reduced
conditions at the mud-water interface, would probably accelerate eutrophication.
The present synoptic study is directed toward identifying the major sources of nutrients reaching
Tahoe and the patterns of eutrophication they produce in the lake. Previous studies proved to be
particularly useful approaches to the problem of identifying nutrient sources and evaluating their
effect on adjacent Tahoe waters. The investigation reported here included primary productivity of
phytoplankton and periphyton as well as examination of species composition, biomass and biotic
diversity.   In  addition,  benthic  invertebrate  organisms  were  collected and their  diversity
determined.

Synoptic studies  are often  made  at  sea where oceanographic vessels collect large numbers of
samples in  transects or over  broad areas. Such collections are limited in their coverage by the time
required for sampling each station  and the slow speed of the vessels between stations. Further,
most  of the marine synoptics cover  days, weeks,  or  months, so that time  and weather are
important  variables.  Some  improvement  is anticipated as automated  sampling and aerial
reconnaissance techniques  are  improved,  but the  limitations  indicated above remain serious
problems. Synoptics covering physical and chemical parameters have been made in the Great Lakes
(e.g. Ayers. et al., 1958, Anderson and Rodgers, 1963, Saunders, Trama and Bachmann, 1962).
Synoptic surveys  of two New Zealand lakes for water chemistry, phytoplankton, and zooplankton
distribution were made  by Fish and Chapman (1969). For primary productivity measurements,
shipboard incubation has long been used for synoptic surveys at sea, and Sorokin (1959) used the
technique in  Rybinskii reservoir over a period of  seven days in June. He found photosynthesis
varied in different parts of the lake as much as tenfold during this period.

Because of the photosynthetic variation from day to day, reflecting changes in the composition of
phytoplankton, nutrients, or weather, a synoptic covering the shortest possible time period will
have the greatest precision  for detecting variation in fertility within the system. The  synoptic
approach of 1968 reported  here was  probably unique  in covering the entire surface layers of a
large lake  in a single day without disrupting the  natural light cycle and with an in situ incubation
of the primary productivity  samples. This eliminated  the uncertainties associated with studies that
covered longer time periods  with various light conditions, or the necessity of using the unnatural

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light of deckboard  incubation.  It provided a nearly  instantaneous measure of productivity, and
phytoplankton composition and biomass over the whole lake.

                                        METHODS

The synoptic approach evolved  from the first series of synoptics done in  1962 to the 1968 series
reported here. In 1962 eight stations were incubated in situ with varying incubation time from
station to station. These were corrected to a daily value on the basis of a diurnal series of samples
run at an index station. In 1967 five different stations on  three different dates were sampled for
comparison of primary productivity. Incubations were done in a rotating incubator under constant
artificial light at surface water  temperature. Samples for  each station were taken at two depths
where  the photometer measurements indicated 75% and 50% transmission of the available surface
light.

The following paragraphs describe the methods used in 1968.

Phytoplankton

In the summer of 1968 three synoptic studies were conducted: synoptic one  during 16-17 July
synoptic two during 11-12 August and synoptic three during 1-2 September.

Thirty stations were selected, twenty-five of which were located along the shore around the lake.
Five stations were  in the middle of the lake. In areas where it was desired to test for steep
gradients in production, three stations were located relatively close together, such  as for General
Creek, Upper Truckee, Cave Rock, and Incline Creek where one station was chosen at the mouth
of the creek and one on each side.

Two boats were used  to collect all the water samples within about a six hour time  period. All the
water samples were collected at night, between approximately 8:30 pm and 2:30 am, and stored in
insulated boxes, so that no photosynthesis or sample warming would take place and so as not to
expose the  organisms to  high surface light  or  disrupt their diurnal rhythm.  Four depths were
sampled: 0 meters,  5'meters, 10 meters, and 15 meters. Water samples were collected in 125 ml
Pyrex bottles for measurements of primary productivity using the carbon-14 method as modified
by Goldman (1963). Phytoplankton and water chemistry samples were collected at the same time.
All samples were returned to the index station located near Homewood on the west shore. This is
near our laboratory where regular in  situ productivity measurements are taken on a year round
basis.

All primary productivity samples were rapidly injected with  carbon-14 solution just before sunrise,
lowered into the lake, and suspended  at the  same depths from whence they were collected. The
bottles were left to  incubate all day and were returned to the laboratory for filtration at sundown;
handling of the  large number of  bottles was therefore accomplished before any  occurrence  of
photosynthesis  and after  photosynthesis  had  stopped in all bottles. This provided an  equal
incubation period for all samples so that the primary productivity measurements for all  stations
were comparable.

Phytoplankton samples were collected for each station by  pooling aliquots from each depth into
one sample. The samples were fixed with neutral Lugol's solution  and returned to  the University

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 4
of California campus at Davis for identification, counting, and measurement of individuals for
determination of their biomass. An inverted microscope was used for this work.

The water chemistry samples for alkalinity determination were taken for each station at the 5
meter depth only, since no significant change with depth down to 15 meters was detected in Lake
Tahoe. Carbon  available for photosynthesis was calculated from these samples by titration with
acid (Saunders, Trama, and Bach ma nn, 1962). We have since gone to infrared CO2 analysis which
is more rapid.

Periphyton

Seventy-nine sampling stations were  chosen around the lake along the shore and samples taken
between  28 March 1968 and  18 September 1968. Periphyton samples were collected on glass
cylinders of 40 mm lengths and 24 mm O.D. Pyrex held by test tube holders at a depth of five
meters. The pieces of glass tubing were cleaned with hot acid and stored in 0.1 N Hcl prior to use.
The length of time required for the development of significant attached growth varied according to
the productivity of the habitat. A week to ten days incubation was found to be adequate at the 5
meter depth  in Lake Tahoe. When the periphyton collectors were retrieved, they were stored
frozen in individual plastic snap cap vials until combusted for total carbon content. Combustion of
periphyton was achieved by placing the tubing in a  .005-inch-thick platinum sleeve in an induction
furnace (LECO Series 521). This rapid method for the determination of the carbon  content of
periphyton depends on the measurement of the combusted carbon in  an infrared  gas analyzer
(Armstrong. Goldman, and Fujita, in press).

Benthos

Thirty-nine locations were chosen, evenly distributed over the lake on a grid, plus one station in
Emerald Bay and one on a "lakemount" (discovered and described by C.R. Goldman and J. Court,
1968). Sampling was conducted between August 1.1968, and October 26, 1968 and served as the
basis for a study of sedimentation in  the lake (Court, Goldman, and Hyne, manuscript). Only one
sample was taken  from each station using a Shipek sampler, so that a high degree of quantitative
reliability cannot be claimed for the collections. The sediment samples collected varied in amount
from less than one liter to more than  four liters, depending on the substrate, and were washed and
sieved before sorting. Lake water was  used for the washing, and care was taken not to cause a
grinding of the  organisms in the washing of the sand and silt. Sieving was graded and fine enough
to prevent the passage of even such small organisms as ctadocerans and copepods. Following the
washing, the samples were  preserved in formalin In smarf vials. The various organisms were then
identified and enumerated.

                              RESULTS AND DISCUSSION

In 1967 the variation in primary productivity, was particularly high in August and September.
Comparisons were not converted  to  mgC/m2/day because they were incubated under  constant
light not very representative of the lake  conditions. Crystal Bay and the South Shore were the
highest stations in August and early  September respectively (Fig. 2). With the onset of winter
storms and mixing, the variation in stations disappeared in late September.

The  1968 synoptics  provided a great deal more data than the 1967 studies. For the synoptic at

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                           AB.-Ago1« Boy
                           SH.-Skunk Harbor
                           S.S.-Sou1h Shore
                           CBrCrystal Bay
                           M-LrMld-Loki
FIGURE 2  Primary productivity measurements taken at five different locations of LakeTahoe,
            on three different sampling periods, at the two depths where 75% and 50% light are
            transmitted.

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each station, primary  productivity for the day, under a square meter surface, for the 15 meter
column  of water, was calculated in mgC/m2/day. A contour  map of primary productivity was
constructed  from this data  (Fig.  3). For synoptic  one,  the  range  of  values was  from 11.04
mgC/m2/day in a midlake station  to 78.52 mgC/m2/day at the mouth of Incline Creek.  For the
second  synoptic, values  ranged  from  12.41 mgC/m2/day  in  a  midlake  station  to 90.86
mgC/m2/day at Tahoe City. For the third synoptic, values ranged from  17.85 mgC/m2/day in a
midlake station to 84.07  mgC/m2/day at the mouth of the Upper Truckee River.

In 1968, during each synoptic study, primary productivity was measured  at 13 different depths at
the index station, and the percentage  of the  primary  productivity of the entire  euphotic zone
represented  by  the  primary productivity  of the  first  15  meters was estimated from  this
comparison.  On that basis, the average primary production of the euphotic zone, extended to 105
m (the average  depth  of the euphotic zone), was found  to be 125.0 mgC/m2/day for the first
synoptic, 109.6 mgC/m2/day for the second, and 193.9  mgC/m2/day for the third.

For each station, the average of the three synoptics was calculated  and a contour map of  primary
productivity  in  Lake Tahoe was drawn based on the average of the three synoptics (Fig.  3). The
range of average values varied by fourfold, from 14.90  mgC/m2/day in a  midlake station to 57.22
mgC/m2/day at Tahoe  City. The  spatial patterns of  primary productivity appeared  to be not
random but  ordered. Primary productivity is often high near shore and at the mouths of creeks. It
is generally low  at stations near the middle of the lake.

The  total number of  individual phytoplankton per ml and the  total fresh weight (biomass) in
milligrams per cubic meter were calculated for each synoptic at each station. Average values for
the three synoptics at each station were used to draw isopleth  lines of phytoplankton on the map
of Tahoe (Fig. 4), as was done for primary productivity. Average values  of number of individual
per ml varied by 4.5 fold, from 20.58 in midlake to 77.08 at the mouth of Incline Creek and 89.33
at Tahoe City. Average of three  synoptics per station for the biomass of the phytoplankton varied
by sixfold, from  19.89  mg/m3  at  Rubicon Point and 20.65  in midlake to 77.71 mg/m3 at the
mouth of Incline Creek and 129.56 mg/m3 at Tahoe City.

Spatial  patterns of  phytoplankton,   like   the  primary   productivity,  appeared  ordered.
Phytoplankton  concentration was  high  near  shore and  at the mouths of some  creeks. It was
systemically  low in the middle of the lake.

Biotic diversity per individual on  the  number of individuals  per species of  phytoplankton was
computed for each station  and each  synoptic.  The  expression for diversity used here is the
information  measure of  diversity   used by Margalef (1957, 1965), Goldman et al. (1968) and
Goldman (1970, in press).
                                  i=m     nj         nj
                           D =   - 2     	  Iog2  	     0
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         17 JULY
         2 SEPTEMBER
                                                    Average of the 3 Synoptics
FIGURE 3   Contour  map  of primary  productivity in the upper  15 meters of water based on
            mgC/m2 /day1  measured at 30 stations for each of the 3 synoptics. The fourth map is
            based on  values at each station which are the average of the 3 values of the individual
            synoptics. X's indicate the station locations.

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                                                                                                                                      CD
Numbn 01 IndMduolt
   Pwml
filomois
mq. m"'
Blotlc Div«r»ily Pir Individual
     Bill Pv C«ll
                    FIGURE 4  Phytoplankton number of individuals, biomass, and diversity per individual. Isopleth
                                lines have been drawn using values at each station which are the average of  the 3
                                individual synoptic values. X's indicate the station locations.

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Average values for  the three synoptics at each station were used to draw isopleth lines of biotic
diversity in bits per individual on the map of Lake Tahoe, as was done for the other variables (Fig.
4).  Average values  of biotic  diversity  per individual varied from 2.61 bits  per  individual in a
midlake station to 3.59 bits per individual at Tahoe City. Spatial patterns of diversity appeared to
be not random but  ordered. Higher values were largely in shallow water areas near shore and at the
mouths of some  creeks where productivity was also higher. Diversity values were systematically
low at some of the deep midlake stations.

A considerable difference between shallow water and deep water productivity and  phytoplankton
concentration is evident from Figures 3 and 4.

A student t  test was used to  determine the significance of this difference between sampling
stations in midlake and those nearer the shore. Four combinations of stations were tested.

     I.    The four  midlake stations of the deep northern part of the lake versus all other stations.

     II.   The four  midlake stations of the deep northern part of  the  lake plus the midlake deep
          station offshore from the Upper Truckee River versus all  other stations.

     III.  The four  midlake stations of the deep northern part of  the  lake plus the three stations
          alongshore off General Creek versus all other stations. General Creek on  the West Shore
          of the lake is a tributary of low nutrient concentration and of small stimulation to algal
          growth (Goldman and Armstrong, 1969).

     IV.  Same as III but including  one  more station south of General Creek close to shore, and
          the  midlake station off  the  Upper Truckee  River  with  the other midlake  stations,
          namely 8 stations, versus the other 22 stations.

Differences in primary productivity, concentration of phytoplankton individuals, concentration of
phytoplankton biomass, and diversity per individual of phytoplankton were tested. Results are
shown in Table  1.  Data from all three synoptics and all thirty  stations per synoptic (90 data
points)  were  used for each t value determination. Significant results were obtained from all four
groupings selected for primary  productivity,  phytoplankton number of individuals, and biomass
concentrations. This indicated that the difference between the means of the two groups of stations
selected in all four  cases was sufficient to warrant the conclusion that the one group with midlake
stations  was  definitely different from  the other. Highest significances, 0.1% and 0.5%,  were
obtained  for  primary  productivity. Grouping arrangements I and  II gave the most  significant
results  for  primary  productivity  and  grouping  IV  gave  the  most significant  results for
phytoplankton concentration. For the data on phytoplankton diversity, differences between the
means of the two particular groups of stations selected in those four cases were not sufficient to
conclude  that one group was different in diversity from the other. This  was probably  due to the
one midlake station on the northwest of the lake where the diversity was quite high.

These results show  the highly  significant differences in  primary productivity between the shallow
and  deep water  stations  of the lake, as well as the difference in phytoplankton numbers and
biomass. Furthermore, they show that primary productivity and phytoplankton concentrations in
the waters along the shore off the General Creek area were not as different from midlake results as
those of the waters sampled offshore near other disturbed, drainage areas. They were more similar

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10
                              TABLE 1  fTEST RESULTS

                   Significance of Difference Between Sampling Stations in
                               Midlake and Along the Shores
 Primary Productivity
   I
Stations
1-25,30
 versus
 26-29

 4.074

 0.1%
   II
Stations
  1-25
 versus
 26-30

 3.906

  0.1%
    III
 Stations
 1,5-25,30
  versus
2,3,4,26-29

  3.286

   0.5%
  TV
Stations
 1,6-26
 versus
2-5,26-30

 3.163

 0.5%
 Phytoplankton No. Individuals
 2,009

   5%
 2.317

  2.5%
   1.862

    10%
                                                                                 2.653
 Phytoplankton Biomass
 1.706

  10%
 1.896

  10%
   1.851

    10%
 2.470

  2.5%
 Phytoplankton Diversity
                                     1.240
                1.477
                                                                  0.388
                                               1.418
 Results from all three synoptics on a total of 30 stations were used for each T value determination.
 Level of significance is for 88 degrees of freedom and is given as percent level under the t value.

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                                                                                       11
to the midlake  deep water stations  than  other  shoreline waters, since grouping  IV also gave
significant results, particularly for primary productivity.

Higher diversity (Fig. 4) was evident in the  shallower water areas of  the  lake as well as in the
vicinity of  streams  where  productivity was higher due to the inflow of nutrients from the
watershed.  This pattern of diversity in Lake Tahoe was observed not only in the average values
from the three synoptics; each synoptic cruise showed  the same general pattern of diversity. The
work of Margalef (1964) suggests that the opposite pattern of species diversity should have been
found. That is, higher diversity occurring in the less enriched, less productive central waters of the
lake and less diversity in the more enriched, more productive shoreward waters of the lake. This
position  is  certainly borne out by our studies  of  a highly productive lake like Clear Lake,
California,   which  at  times  may be  almost  a  monoculture of  bluegreen   algae  such   as
Aphanizomenon. However,  in highly  oligotrophic environments such as Tahoe, a eutrophicating
influence such as fertile stream water may  increase the diversity in the immediate area. Similarly,
benthic forms  may  enter the  lake directly from  the streams. The relative importance  of these
benthic forms to the number of individuals, the biomass of the phytoplankton and directly to the
diversity values  was determined. Out of  the  one  hundred  and three different  species   of
phytoplankton found most commonly in Lake Tahoe,  nine were most likely to be benthic forms
that became dislodged from  their attachment  by  wave  action  or otherwise  freed from the
substrate. These  were mainly diatoms and  included Cocconeis placentula, Cocconeis disculus,
Gomphonema parvulum, Gomphonema capitatum, Cymbella ventricossa,  Cymbella  lanceolata,
Cymbella cuspidata,  and Diatoma  vulgare. Some Anabaena have also been found in the benthos  of
Lake Tahoe. The percentage of those species found in the total phytoplankton population in terms
of number  of individuals and biomass was calculated at each station for each synoptic study. The
same percentages were also calculated from the average values of the three synoptics in number  of
individuals  and biomass at each station. Those results are  shown  in Figure 5. A comparison  of
these results with a bathymetric map  of the lake does not show a very close correlation between
shallow water and high percentage of  benthic forms.  Conversely, deep waters and low percentage
of benthic  forms are not closely correlated,  although  the highest percentages are found in the
shallower waters. This may in part be due to the fact that shallow waters are only a small part of a
lake whose mean depth is  313 meters. The curious pattern  of diversity in Crystal Bay may well
reflect  the deep canyon running out from shore where  benthic forms may not enter the catch so
frequently. Wind patterns  and water  movements  might also influence the presence  of  benthic
forms in the phytoplankton population of the different areas of the lake, as might the nutrient
history of existing periphyton of  the various areas. This is  particularly true if we consider that
periphyton has only  become abundant in the  lake  during the last ten years as the nutrient content
of littoral water has  accelerated  its growth. Comparing  these results with the biotic  diversity per
individual did not show a systematic relationship.  To verify and further investigate this, the biotic
diversity per individual was calculated again  for each synoptic cruise and for the average of the
three, but this time omitting the benthic species. All  new values  were lower than those obtained
from  the  entire  phytoplankton  population,  but the  overall pattern  of diversity of the lake
remained essentially unchanged.

Rate of growth of periphyton varied from .094 mgC/m2/day, north of Skunk Harbor between 20
July and 18 August, to 2.228 mgC/m2/day, 70 yards offshore north  of Sand Harbor between 15
July and 23 July. Periphyton growth was found to be a function of both the location and the time
of incubation period  (Fig. 6).

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12
         2 SEPTEMBER              S '                AVERAGE OF THE  J SYNOPTICS


                                                  SCALE
                                    STATION LOCATION , 10* NUMBER Of INDIVIDUALS
                                                  JO* BIOMASS


FIGURE 5   Percent number of individuals and  percent biomass of benthic forms of algae found
             in total phytoplankton counts, for each synoptic study and on the average.

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A high  initial  loss of  samples from  periphyton  stations  resulted  in  considerable variation in
effective sampling effort. Later the original surface floats were all replaced with underwater floats
tended  by scuba divers. As a result of loss of stations, quite a few values for the rate of growth of
periphyton were missing from the overall matrix of data which consisted of rows of stations versus
columns of incubation  periods.  In order to be able to determine variations of rate  of growth of
periphyton between areas along the shores of the lake, three types of computations were made.
                                    TAHOE  PERIPHYTON 1968
                       Pinodi of incubation
                       O J»l» I*—July 29
                         Jul, I8-A00..7
                         Jul,20-Aiig. 18
                         AugJS-Stpt. I
                         Aoo.28-S.pt. 13
                                                           Periods of incubation
                                                           ^. June 18 —July 17
                                                             June is-July 10
                                                             July 4 — July 18
                                                                0—July '*
                                                                5 -July 23
                              FIGURE 6   Periphyton rate of growth

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 14
First, adjacent stations of similar productivity were pooled and averaged to give one value for that
particular area  for  the  period  of  incubation (pooling of rows  of  the  matrix). Seventeen main
stations resulted from this  sample pooling. Second, periods of incubations adjacent in time and
showing similar rate of growth for most stations were pooled to give an average rate of growth for
the entire  period  (pooling  of  columns of the matrix). Third,  missing values for one  of the
seventeen main stations  at one of the resulting five periods of incubation were interpolated from
the other values. Interpolations were made favoring rows rather than columns, namely using more
points in time than  stations, rather than a large number of stations and fewer points in time. After
completing the matrix of 17 stations and five incubation periods, columns were averaged to give
one average value of rate between 28 March and  18 September 1968 (Fig. 6). These results vary
between  .343 mgC/m2/day  northeast of the Upper Truckee River to 1.010 mgC/m2/day south of
Tahoe City.

The average daily amount of growth of  periphyton on the bottom of the entire lake was estimated
by use of a planimeter for each area between  the shore and the 100-meter depth, multiplying the
rate of growth of that  location by the area found, and summing  up the results. The weight of
carbon of algae was estimated to be 13% of the total fresh weight of the algae. On that basis the
average total fresh weight of periphyton added daily to the bottom of the lake (by photosynthesis
on the bottom surface only) was found  to be about 576.8 kilograms. This was an underestimate of
the bottom average  daily growth of periphyton, since no correction was made to account for the
irregularity of rock surfaces. Fox, J. L.r Odbug, T.  O. and Olson, T. A. (1969), found in western
Lake Superior that, "After  forty-six days of regrowth on artificially  denuded rocks in Stony Point
Bay, the  growth level was approximately eighteen percent of that occurring naturally." Assuming
this result valid for  Lake Tahoe would  have meant that there are about 147,397 kilograms (fresh
weight) of  periphyton  in Lake Tahoe  (about 147 metric tons).  For purposes of comparison the
biomass of planktonic algae was calculated by averaging biomass per square  meter for the three
synoptic  dates, which resulted  in an estimate of 2,180 metric tons  in the upper euphotic zone of
the lake.

Thirty-three different genera representing a total  of  twelve different classes of animals were
identified in  the benthos  samples (Table 2). Two genera composed 46.6% of all identified
organisms. The dominant organism found in 30 of the 41 stations was Stygobromus (Amphipoda).
A total of  219 of these identified, which represented 27.5% of all the identified organisms and
24.5% of all organisms found. The second dominant organism found in 26 stations wasCandona
(Ostracoda). One hundred and fifty two were found which represented 19.1% of the identified
organisms.

The total number of organisms found in any one sample varied from 0  to 79 (Fig. 7). Values of
diversity  per  individual  were computed for each  station and varied  from  0 to 2.94 bits per
individual (Fig. 8).

Values of diversity per individual for our data on benthos were probably more relevant than total
number of  individuals per sample, due to the limited number and difficulty of obtaining samples
of comparable size.

-------
                                                                                       IE
                              DIAMETER SCALE
                              _J1120INOIVIDUALS
FIGURE 7   Lake Tahoe 1968 Benthos - Total Number of Individuals Per Station Per Sample
                            DIAMETER SCALE
                            ,_, I BIT PtR INDIVIDUAL
                 FIGURE 8  Lake Tahoe 1968 Benthos Diversity Per Individual

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 16
                                     TABLE 2
                        Organisms Found in the Benthos Samples
CLASS

Protoza


Turbellaria




Nemata




Oligochaeta
Ostracoda


Copepoda
Malacostraca
 Amphipoda
GENERA

Tetrameris
Phagocata
Dendrocoelopsis
Rhynchoscolex
Trilobus
Dorylaimus
lotonchus
Peloscolex
Lumbriculus
Limnodrilus
Herdea
Ilyiodrilus
Rhynchelmis
Haplotaxis
Naidium (Breviseta)
Eisentetta
Aeolosoma
(Immature)
(Newly hatched)
(Cocoons)
(Eggs)
Candona
Diaptomis (Tyrelli)
Epishura
Stygobromus
Hyalella
(Decomposed)
(Unidentified)
  NO. OF
 STATIONS
ORGANISMS TOTAL NO.
 PRESENT    ORGANISMS
     20
     1
     1
     8
     8
     8
     19
     3
     4
     2
     5
     3
     1
     1
     1
     1
     3
     4
     9
     2
     26
      1
      1
     30
     9
     2
     2
79
 3
 1
 25
 23
 20
57
26
24
19
13
 8
 5
 2
 2
 1
19
20
24
 2
152
 37
 3
219
28
 2
 2
                % OF
            TOTAL  NO.
             ORGANISMS
                                                        .8
                                               83      9.3
                                               68      7.6
222     24.9


152     16.9



40     4.5
                                                                   251     28.2
Insecta (Chironomidae) Orthocladiinae *             6
                     Procladius                  2
                     Chironomus (Atritibia)       1
                     Phaenopsectra              1
                                       17
                                       2
                                       1
                                       1

-------
                                                                                     17
CLASS

Insecta (Hecoptera)
Acari
Mollusca
  Gastropoda
Pelecypoda

Terrestrial Arachnid

Miscellaneous
                                   TABLE 2 (Cont'd)
                         Organisms Found in the Benthos Samples
GENERA

Capina

(Terrestrial Gnat)
(Midge)
(Larva)
(Diptera Adult)
(Unidentified)
Lebertia
Limnochares
Parapholyx
Gyraulus

Pisidium

Arachnida *

Eggs
Cocoons
  NO. OF
 STATIONS
ORGANISMS  TOTAL  NO.
 PRESENT    ORGANISMS
                % OF
            TOTAL  NO.
             ORGANISMS
      2
      1
      1
      1

      2

      1

      9
      1
 2
 1
 6
 1

4.4

 1

 18
 3
33       3.7



 3       .3




 7       .8


         .1



21       2.3
                                              Total No. of Organisms Found   892
*Not identified to Genus
                                     CONCLUSIONS

 The  synoptic approach  is  very  useful  in studying cultural eutrophication, as it enables the
 investigator to accurately locate sources of nutrients before the entire lake has undergone change.
 Lake Tahoe showed several areas  of increased fertility. These were at the South Shore under the
 influence of the Truckee River drainage and high resident population, in Crystal Bay where Incline
 Creek and Third Creek drained highly disturbed land, and near the outflow of the lake where there
 were both a high resident population and fairly extensive areas of shallow water.

 Despite the lake's great volume for dilution of the annual  inflow, local nutrient sources are altering
 the productivity pattern around the lake. A spring bloom of algae, which actually turned a path of
 Tahoe's  traditionally  blue water green,  has already been  observed at the south  shore  and
 periphyton growth has become luxuriant around the entire lake margin during the last decade. In
 August 1969, following extensive land disturbance associated with construction  of a golf course
 and a subdivision, Third Creek was found  to be extremely stimulating to growth of Tahoe algae. In
 the experiment summarized in  Figure 9, 10% of this  stream water added to  Tahoe's natural
 phytoplankton  population  stimulated  photosynthesis  by over  600%. When  compared with

-------
 18
controls. Incline Creek and the Upper Truckee River were also notable lake fertilizers in contrast
to relatively undisturbed General Creek. This is not surprising since the Incline Creek drainage has
been recently subdivided for homes and the Upper Truckee River and some of its tributaries have
also suffered considerable disturbance. Further, this drainage was used for some time as a  land
disposal site for treated sewage. The sewage is  now being exported out of the basin, but the  land
disposal site still provides a drainage high in nitrogen.

Although occassional high periphyton values are encountered near tributaries, there appears to be
less correlation with  tributaries than  was found for phytoplankton productivity and biomass. In
general, distribution of periphyton is fairly uniform around  the lake. This probably reflects the
steady movement of water over the littoral zone of the lake which distributes the nutrients rather
uniformly to these sessile forms.

The results of our study of the possible relationship between diversity and benthic forms can only
be considered as a preliminary  investigation since our list included only those  species that were
most likely to be found in the periphyton of Lake Tahoe. Further, more detailed observation of
the lake's periphyton species composition at the time of the study  would have been a valuable
addition.

From the above results we can say that benthic forms of algae contribute overall to increase the
diversity per  individual of the  Lake  Tahoe phytoplankton  communities, but  that they do not
appear to be the major determinants of aerial variation in diversity.
740 -]
700-
t 660-
| 620-
« 580-
f 540-
| 500-
« 460-
« 420-
u
£ 380-
S« 340-
i 300-
2 260-
| 220-
S 180
"5 140
o>
< 100-
RD-





' 0-eek
lociifift
Village



LAKE TAHOE
August 12, 1969




Incline
Creek
Incline
Village

Mfcrtr
Truckee
River
Shore Cr*efc
Unpolluted
• '< • Cpntol -
                              10% STREAM WATER ADDED TO LAKE WATER

FIGURE 9  Fertilization  of Lake Tahoe water from a  10% addition of four of its tributaries.
            Algal growth rate was measured with the natural Tahoe population by radioactive
            carbon  uptake. Highest biostimulation was measured  in  Third  Creek following
            disturbance of its watershed. General Creek, which drains an area of undisturbed
            land, is used as control.

-------
                                                                                      19
The results of the benthic survey are the most difficult to interpret, for there does not appear to
be a systematic pattern to either the distribution of numbers of organisms or the distribution of
biotic diversity. This condition is especially evident when compared to the  synoptic surveys of
primary productivity where the primary productivity  rate increased sharply  near the mouths of
some of the creeks. It is quite possible that the lack of pattern in the benthos data may be a result
of the lack of replicated samples and the small and variable sample sizes. However, the abundance
and diversity of the benthic organisms may  not be functions of the same environmental property
as the abundance,  productivity and diversity of the phytoplankton. Algae are clearly associated
with the mouths of creeks and their productivity has been shown to be stimulated by additions of
creek water (Goldman and Armstrong, 1969). The environmental factors that affect the benthos
have not been determined, and a lack of pattern in benthic numbers and diversity may be an
indication  that nutrient  enrichment is not a primary  factor  limiting the abundance of various
species of benthos.

Tahoe  is  unquestionably changing. The  synoptic approach provides  a  nearly  instantaneous
evaluation of conditions as they exist on a given day. Close monitoring of wind and currents could
add further to our understanding of water transport in the lake as it affects the presence of more
fertile areas. In general, the primary producers must be viewed as a more sensitive  indication of
increased fertility than chemical parameters, since any additional nutrients appear to  move rapidly
into the  phytoplankton.  We  characteristically find little  or no measurable  change in water
chemistry  (unpublished data) while phytoplankton  photosynthesis is showing  a very significant
change. If the quality of our lakes is to be conserved, synoptic studies can be a great aid in locating
and defining the influences of nutrient  sources. When combined with  bioassays, the  relative
stimulation  of  the various  sources  can  be  quantified and  corrective measures  taken  before
accelerated eutrophication destroys the quality of the environment.

                                  ACKNOWLEDGMENTS

The authors wish to acknowledge the valuable field assistance of James Court, Gordon Godshalk,
Richard Armstrong, and  Peter  Richerson.  Frank  Sanders  sorted  and identified  the benthic
organisms  and Anne Sands handled the phytoplankton taxonomy  and counting. Denne Bertrand
and Noel Williams gave valuable assistance in data reduction. Elisabeth Stull provided valuable aid
in preparation of the  final manuscript. The work  was  supported by FWPCA  grant (now FWQA)
No. DBU 16010 to the senior author.
                                      REFERENCES
Abrahamsson, S. A. A. and Goldman, C. R. (1970) The distribution, density, and production of
     the crayfish, Pacifastacus leniusculus Dana in Lake Tahoe, California-Nevada, Oikos 21:1-9.

Anderson, D. V. and Rodgers, G. K. (1963) A synoptic survey of Lake Superior. Great Lakes Res.
     Div., Univ. Mich. Pub. No. 10:79-89.

Armstrong, R., Goldman, C. R. and Fujita, D. K. (1970) A rapid method for the estimation of the
     carbon content of seston and periphyton. Limnol. Oceanogr., In Press.

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 20
Ayers, J. C., Chandler, D. C., Lauff. G. H., Powers, C. F. and Hensen, E. B. (1958) Currents and
    water  masses of Lake  Michigan. Great  Lakes Research Institute, Univ. Mich. Pub. No.
    3:1-169.

Court, J. E., Goldman, C. R.  and  Hyne,  N. J. (1970)  Surface  sediment in Lake  Tahoe,
    California-Nevada. (Submitted manuscript).

Fish,  G.  R. and Chapman, M. A. (1969) Synoptic surveys of lakes Rotorua and Rotaih. N.Z. J.
    Mar. Freshwat. Res. 3:571-84.

Fox, J.  L., Odlaug, T. O. and  Olson,  T. A. (1969) The ecology of periphyton in Western  Lake
    Superior. Water Resources Research Center, Univ. Minn., Bull. No. 14:1-127.

Frantz,  T.  C. and Cordone, A.  I.  (1967) Observations on  deepwater plants in Lake Tahoe,
    California and Nevada. Ecology 48:709-714.

Goldman, C. R.  (1963) The  measurement  of primary productivity and limiting  factors  in
    freshwater with  Carbon-14.  In:  M.S.  Doty  (ed.),  Proc.  Conf.  Primary  Productivity
    Measurement, Marine, and Freshwater, U.S. Atomic Energy Commission, Tl0-7633:103-113.

Goldman, C.  R. (1964)  Primary  productivity  and  micro-nutrient limiting factors in some North
    American and New Zealand lakes. Verb. Internal. Verein. Limnol., 15:365-374.

Goldman, C.  R. (1967) Integration of field and laboratory experiments in productivity studies. In:
    George H. Lauff, (ed.). Estuaries. Publ. No. 83, AAAS, Wash., D.C., p. 346-352.

Goldman, C. R. (1968) Aquatic primary productivity. American Zoologist, 8:31-42.

Goldman, C. R.  (1970) Photosynthetic  efficiency and diversity  of a natural  phytoplankton
    population in Castle Lake. Proc. Trebon IBP/PP Symposium. In  Press.

Goldman, C.  R. and Armstrong R. (1969) Primary  productivity studies in Lake Tahoe, California.
    Verh. Internal. Verein. Limnol., 17:49-71.

Goldman, C. R. and Carter,  R.  C. (1965) An investigation by rapid C-14 bioassay of factors
    affecting the  cultural eutrophication of Lake Tahoe, California-Nevada. J. Water Poll. Control
     Fed., 37:1044-1059.

Goldman, C.  R. and Court, J. (1968) Limnological studies of Lake Tahoe. In: Geologic Studies.
    Guidebook of Geol. Soc. Sacramento, 60-66.

Goldman, C.  R., Gerletti, M., Javornicky,  P. Melchiorri-Santolini, U. and de Amezaga, E. (1968)
    Primary  productivity, bacteria, phyto and zooplankton in Lake  Maggiore: Correlations and
    relationships with ecological factors. Mem. 1st.  Ital. Idrobiol., 23:49-127.

Goldman, C.  R., Tunzi, M. and Armstrong, R. (1969) Carbon-14 uptake as a sensitive measure of
    the growth of algal cultures. FWPCA Symposium, Berkeley, June 1969, 158-170.

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                                                                                     21
Hutchinson, G. E.  (1937) A contribution to the limnology of arid regions primarily founded on
    observations made in the Lahontan Basin. Trans. Conn. Acad. Arts. Set. 33:47-132.

Juday, C.  (1907)  Notes on  Lake  Tahoe. its trout and  trout fishing. Bull.  U.S.  Bur.  Fish.,
    26:133-146.

Kemmerer, G., Bovard, J. F. and Boorman, W. R. (1923) Northwestern lakes of the United States.
    Bull. U.S. Bur. Fish., 39:51-140.

LeConte, J. (1883a) Physical studies of Lake Tahoe -1. The Overland Monthly,1:506:516.

LeConte, J. (1883b> Physical studies  of Lake Tahoe - II. The Overland Monthly, 1:595-612.

LeConte, J. (1884) Physical studies of Lake Tahoe - III. The Overland Monthly.3:41 -46.

Margalef,  R. (1957)  La  teria  de la informacion  en ecologia. Mem. R. Acad. Cie. y Artes de
    Barcelona, 32:373-449.

Margalef,  R. (1965) Ecological  correlations and the relationship between primary productivity and
    community structure. Mem. 1st. ItaL Idrobiol., 18 Suppl.:355-364.

Saunders, G. W.,  Trama,  F. B. and Bachmann, R. W. (1962) Evaluation of a modified C14
    technique for estimation of photosynthesis in large lakes. Great Lakes Res. Div. Univ. Mich.
    Pub. 8:1-61.

Sorokin,  Y. I.  (1959) Determination of the photosynthetic productivity  of phytoplankton in
    water using C14. Fiziol. Rast. (U.S.S.R.), 6(1):125-133.

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                  THE SOUTH  BASIN  OF LAKE WINNIPEG
                        AN ASSESSMENT OF  POLLUTION
                                  Jo-Anne M. E. Crowe
                                    INTRODUCTION

During their brief geologic life, lakes are subjected to a variety of physical and biological processes
which  result in their ultimate extinction (Powers and Robertson, 1936; Robertson and Alley,
1966). This is  a natural, slow process termed eutrophication. Eutrophication  accelerated or
augmented by man's activities may be termed pollution.

Classical  studies on lake eutrophication  include those by Minder  (1926), Hasler (1947) and
Edmondson, Anderson  and Peterson (1956). The most intensive studies on the North American
continent have involved the Great Lakes and particularly Lake Erie (Wright, 1933; Brown, 1953;
Powers et al., 1959; Beeton, I960, 1961, 1963 and 1966; Matheson,  1962; Wood,  1963; Carr and
Hiltunen, 1965; Matheson, 1965; Powers and Robertson, 1966; Arnold, 1969).

Lake Winnipeg possesses many features which render it comparable with Lake Erie. Both are large
Pleistocene  lakes of recent origin. In size Lake Erie ranks 13th and Lake Winnipeg 14th among the
freshwater lakes of the world. Both are  adjacent to major population centers. Both are employed
as transportation  systems  to varying degrees. The commercial fishery of both lakes provides a
major source of food and revenue. Finally, both lakes have served as recreational areas.

In contrast  to the abundance of published literature dealing with Lake Erie, little material dealing
with general  limnology is available for  Lake  Winnipeg.  Bajkov (1930) studied the chemical
composition of Lake Winnipeg waters  and the  benthic  composition. Studies on the mayflies of
Lake Winnipeg were published by Neave (1932). Slack (1967) studied the benthos of certain lakes
in Manitoba whose basins were located astride Precambrian and Paleozoic bedrocks. Einarsson and
Lowe (1968) studied seiche cycles on Lake Winnipeg and Anon., (1969a) reviewed the problems
associated with fluctuating lake levels.  An assessment  of the possible effects of pollution  on the
benthos was presented by Cover (1966).

It is worthy to note that Butler (1949) said, "Pollution of  waters inhabited by fish is not yet a
major problem in  Manitoba." It is our contention that this problem has arisen  in  Lake Winnipeg
and that  the lake is undergoing a eutrophication cycle  similar  to that of Lake Erie. The main
evidence  for increased  eutrophication  due to pollution is evident  in  the changes which have
occurred  in  the benthic fauna since 1930.

                             DESCRIPTION OF THE AREA

Morphology and Morphometry

Lake Winnipeg lies between 50° 22' and 53° 38' north Latitude and between 96° 11' and 99° 09'
west Longitude in the province of  Manitoba (Fig. 1). The surface area is approximately 9,230
square  miles (23,905.7 km2). Thus it  ranks as the third largest wholly Canadian lake and the
largest in  the province of Manitoba.

                                          22

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                                                                                       23
     FIGURE 1  Province of Manitoba, showing major lakes, rivers, cities and geologic zones
The lake is oriented  in a northwest-southeast direction and spans a distance of 253 miles. It is
divided  naturally into three areas, a north basin with a maximum width of 70 miles and a mean
depth of 49 feet (15m), a channel area with a maximum width of twelve miles  and a maximum
depth of 60 feet (18.2m), and a south basin with a maximum width of 27.5 miles and a maximum
depth of 40 feet (12.2m).

Geology

Due to  its geologic history and structure, Lake Winnipeg has unique qualities. First, it is a glacial
lake  of  recent origin having  assumed  its present form approximately 5,000 years ago (Elson,
1958).  At  present,  with  neighboring  Lake Manitoba and  Lake Winnipegosis,  Lake Winnipeg
remains  as the largest remnant of glacial Lake Agassiz  (Fig.  1). Second, the contact line between
Precambrian and Paleozoic  bedrock lies within the  basin of Lake Winnipeg adjacent to the east
shore  (Fig.  1). The latter situation insures that there will be variability both in the composition of
the influent waters and  the fauna. These aspects have been investigated in this and similar lakes
(Rawson, 1953 and 1960; Oliver, 1960; Fedoruk, 1964; Larkin, 1964; Slack, 1965 and 1967).

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 24
Watershed and Drainage

The drainage area  for Lake Winnipeg is 370,000 square miles (958,300 km2) exfending through
portions of four provinces and three states. The major influent rivers are the Saskatchewan from
the west and the Winnipeg from the east {Fig. 1). The former contributes 39% of the total drainage
receipts and the latter 32% (Anon., 1969a). From the south, the Red River contributes 6% of the
total inflow while  the  remaining 23% is provided by numerous streams and rivers arising in the
Precambrian area to the east. Major drainage from the west is scanty and consists primarily of the
Saskatchewan  River and the Dauphin River (Fig. 1). The lake is drained by the Nelson River to the
north into  Hudson Bay (Fig.  1). In addition to the major influent sources,  considerable water
moves between the lake basins as seiches (Einarsson and Lowe, 1968).

Sources of Pollution

There are three potential sources of pollution for the south basin of Lake Winnipeg. The first is
run-off  from agricultural  land to the south and west and is undoubtedly a major contributor
(Personal communication. Dr. G. Brunskill, Freshwater Institute, Fisheries Research Board of
Canada, Winnipeg).

The second is the  city of Winnipeg which is located at the junction of the Red and Assiniboine
Rivers approximately 35 miles south of Lake Winnipeg (Fig. 1). Urban population has risen from
293,300 in 1931  to 515,661  in  1969 (Personal  communication, Mr.  A. S. Bready, Metro
Information, Winnipeg).  In  the  1930's, all  domestic  sewage  and industrial effluents  were
discharged untreated in  the rivers. This situation has gradually been  rectified  and at present most
municipal and industrial wastes receive treatment in activated sludge plants or aerated lagoons. The
total capacity of these systems is 114 million gallons per day. By 1972, all wastes will be treated to
effect a 90% removal of B.O.D.  and suspended  solids (Personal communication, Mr. A. Penman,
Waterworks and Waste Disposal Division, Metropolitan Corporation of Greater Winnipeg).
The third potential pollution source is Abitibi  Manitoba Paper Limited on the Winnipeg  River
approximately 6 miles east of Traverse Bay (Fig. 1). The sole product is newsprint produced by a
sulfite  process. Water consumption  in the plant is 11,100,000 Imperial gallons/day. Treatment
facilities serve to remove bark and fibre. All effluents from the plant, except domestic sewage, are
discharged into the Winnipeg River.  B.O.D. values of  7.9 ppm and dissolved oxygen values of  6.7
ppm have been recorded in the river adjacent to the discharge site. Downstream the B.O.D. was  3.1
ppm and dissolved  oxygen 10.0  ppm  (Personal communication,  Mr. D.  D. Munro, Abitibi
Manitoba Paper Limited, Pine Falls).

                              METHODS AND MATERIALS

Sampling Procedures

A four-mile grid pattern was adopted for sampling in the south basin of Lake Winnipeg (Fig. 2).
Sampling was performed twice each year; in March during  the period of winter stagnation and in
September, the  autumnal overturn. The scope  of the sampling schedule from  March, 1962 to
September, 1969 is summarized in Table  1. Winter sampling was conducted by bombardier and
autumn sampling by the Manitoba Fisheries Branch research vessel. The locations of transects were

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                                                                                    25
 determined by shore landmarks and compass bearings (Fig. 2). Station positions were located by
 odometer in the bombardier and by a combination of time and engine speed on the research vessel,

 Limnological data routinely collected on location included water depth, surface and bottom water
 temperatures, dissolved oxygen, alkalinity, free carbon dioxide and pH. Turbidity was measured
 by Seichi disc to the nearest %-foot in the ice-free periods. Ice thickness was recorded in the March
 periods.
Month


March

September

March

September

March

September

March

September

March

September

March

September

March

September

March

September
                         TABLET

Lake Winnipeg Sampling Schedule. March 1962 to September 1969

       Year              Number of Stations              Grid Lines Sampled
       1962

       1962

       1963

       1963

       1964

       1964

       1965

       1965

       1966

       1966

       1967

       1967

       1968

       1968

       1969

       1969
 70

 63

 22

 63

 40

 73

 39

 66

 20

 65

 16

 34

20

33

20

34
 AtoN

 AtoG

 A, F and K

 AtoN

 AtoP

 AtoN

 AtoF

 AtoN

 AtoD

 AtoN

 AtoD

AtoN

AtoD

AtoN

AtoD

AtoN
Water depth was measured to the nearest Vi-foot by  a graduated sounding tine. These were
confirmed by  a  model D-11  Bendix  depth recorder. Prior to 1967, water temperatures were
measured by a brass-encased thermometer in degrees Fahrenheit. Subsequent to this, hydrographic
thermometer has been employed. Alkalinity and free carbon dioxide values were determined by
standard titration methods (Anon., 1965). pH was determined by comparator using phenol red.

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 26
                                                        0 Hentey Rittr

                                                       Traverse Boy
                                 12345  67

            FIGURE 2   Four-mile grid sampling pattern. Lake Winnipeg south basin

pH range 6.8 to 8.4, as indicator.

Two-litre  bottom  water  samples  were  collected  by  1,200  cc  Kemmerer  sampler  from
predetermined stations during each period. Analyses for a maximum of 20 factors were performed
by the Provincial Environmental Health Laboratory in Winnipeg

During all periods except September 1964 and September 1967, a standard 9-inch Ekman dredge
was employed to collect benthos,  fn September 1964 a Petersen dredge  was employed, and  in
September  1967 a Ponar dredge  was employed. The Petersen dredge sampled 0.071 m2  and the
Ponar 0.0518 m2, as compared with 0.0523 m2 sampled by the Ekman. Triplicate benthic samples
were routinely taken at each station except in March 1962, September 1964, and September 1968.
Single dredge hauls were taken in March  1962.  Duplicate samples were  taken  in September 1968
and September 1964, with the exception of four stations in the latter year. At each of  these
stations six samples were obtained.
Prior to 1967, benthic samples were individually retained in 50-pound capacity polyethylene bags.
Whenever  feasible, the  samples  were concentrated by  washing through  a galvanized bucket
equipped with bottom  and side screens constructed of U.S. No.  30  mesh (Fremling, 1961). The
benthos and  remaining debris  were placed in four  ounce  jars containing 10% formalin as
preservative. Samples not concentrated in the field were  frozen and shipped to Winnipeg where the
process was carried out in the Fisheries Laboratory.

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                                                                                     27
 Since  1967,  an 18-inch diameter hoop net constructed of Nitex  nylon has been  used to
 concentrate the samples. The nylon employed has 62 meshes/inch with a mesh opening of 0.0098
 inches (0.2450 mm) and is comparable to a No. 50 U.S. screen.

 The use of Rose Bengal stain and preservative in the samples after initial concentration has aided in
 sorting and enumeration of benthos (Mason and Yevich, 1967). This has proven  to be more
 effective than flotation  techniques,  particularly for  nematodes (Ladell,  1936; Lyman, 1943;
 Birkett, 1957; Anderson, 1959).

 Laboratory Procedures

 In the laboratory, benthic samples were further  concentrated by washing through a No. 50 U.S.
 bronze screen. The remaining were placed in an enamel pan and scanned by a Luxo light with
 magnifier to facilitate separation of benthos into taxonomic groups and enumeration. Members of
 the orders Gastropoda, Ephemeroptera, Amphipoda, Trichoptera, Conchostraca and  the families
 Sphaeriidae and Unionidae were examined with a binocular microscope for taxonomic purposes.

 Whole mounts were  made of  the  Nematoda,  Chironomidae  and Oligochaeta using  CMC-10
 mounting medium.1 The heads of the chironomid larvae were  severed from the bodies at the
 thoracic suture and mounted ventral side uppermost. Corresponding bodies were mounted  in a
 lateral position on the same slide (Curry, 1962).

 Specialized dissecting techniques were required to display the oligochaete reproductive systems for
 species identification (Brinkhurst and Cook, 1966). Modifications were made replacing Euparal or
 Canada balsam  with Amman's fluid,  a  temporary mounting medium  (Personal  communication,
 Mrs. M. Moore (Simmons), Zoology Department, University of Toronto).

 Where possible,  identification  was made to genus. Species identification  of chironomids  and
 oligochaetes was  required. Taxonomic references were as follows: Chironomidae (Johannsen,
 1937; Townes. 1945; Johannsen et a!.,  1952; Robach, 1957; Curry,  1954,  1958 and  1962; Beck
 and Beck,  1966; Mason, 1968); Ephemeroptera (Neave,  1932; Leonard  and Leonard, 1962);
 Oligochaeta (Brinkhurst,  1963 and 1965; Brinkhurst and Cook, 1966); Gastropoda, Sphaeriidae,
 Hirudinea,  Nematoda, Amphipoda,  Conchostraca, Chaoborinae and  Trichoptera  (Ward  and
 Whipple, 1959).
                                       RESULTS

While other lakes possessing similar morphometric characteristics and geologic structure are termed
oligotrophic or at best mesotrophic. Lake Winnipeg exemplifies a eutrophic state (Northcote and
Larkin,  1963). Evidence for this is provided by the chemical composition of its water, benthic
standing crop, benthic composition and commercial fish production.
     1 Mention of commercial sources does not constitute endorsement by Manitoba Department
of Mines and Natural Resources.

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 28
 Physical and Chemical Data

 Mean values and ranges for chemical data  compiled from March  1962 to September 1969 are
 presented in  Table 2. Detailed  results for each  sampling period are provided in Appendix 1.
 South-north gradients for all factors except pH have been noted. Values recorded at stations on
 the A grid line are four times greater than the mean for that period and as high as 30 times greater
 than the minimum values recorded (Appendix 2; Fig. 2). Similar west-east gradients occur for
 factors such  as  calcium, magnesium  sodium, total  hardness,  bicarbonate, carbonate, chloride,
 sulphate  and total solids. Individual values along grid 1 are twice as large as those along grid lines
 adjacent  to the  east shore  (Fig. 2).  For the period March 1962 to September 1969, maximum
 values for most chemical components were recorded during 1966 and 1967 (Appendix  1).

 Dissolved oxygen values normally represent  saturations of 80% or greater during all periods (Table
 2; Appendix 2).  B.O.D. values are consistently  lower than dissolved oxygen values (Table 2). No
 decrease  in oxygen concentration occurs as water depth  increases.  No permanent thermocline
 forms and surface water temperatures are normally less than 2° F higher than those at the bottom.

 Bottom deposits over the portion of the south basin under study consist of a sand-silt-clay mixture
 in the following  mean proportions: sand - 3%, silt - 31% and clay - 66% (Personal communication,
 Mr. W.  Michalyna, Canada Department of  Agriculture, Winnipeg). Highest proportions of  sand
 were found at stations E-1 and N-5 (Fig. 2). The highest proportion of silt was found at station
 A-3  and clay  at stations F-3, G-3 and  H-3 (Fig. 2). A definite south-north  gradient could be
 detected with respect to the silt component. Values for silt on the A grid line are from two to
 three times the mean level and values of those on grid lines L, M and N (Fig. 2).

 Benthos

 Values for benthic standing crop are  based on 102, 105 and 111 samples taken in the south basin
 of Lake  Winnipeg during June, July and  August,  1967,  respectively. The three dry  weights,
 including  mollusc shell, were 88.18 kg/ha, 56.7 kg/ha and 52.24 kg/ha. Mean  standing crop was
 65.7 ± 3.93 kg/ha.

 Between  March  1962 and September 1969, the major  benthic groups were Chironomidae 40%,
 Gastropoda 15%, Oligochaeta 14%, Ephemeroptera 13% and Sphaeriidae 4% (Table 3). The group
 identified as "others" included representatives from six orders and two families which, combined,
 comprised a lower percentage than any single group (Table 3). From March 1968, due to increased
 numbers, it was necessary to consider the Nematoda as a separate group.

 Members of four subfamilies were among the Chironomidae identified (Appendix 2). A total of 41
 genera and species were identified; 24 (59%) belonged to the subfamily Chironominae, 10 (24%)
 to the subfamily Tanypodinae, 6  (14%) to the subfamily Orthocladiinae and  one  (3%) to the
 subfamily Diamesinae.

Two  species  of mayfly  nymphs, Hexagenia limbata occulta  (Walker) and  Hexagenia rigida
 (McDunnough) were identified (Neave, 1932). 94% of the nymphs were H.  limbata and 6% were
H. rigida. The ratio of females to males was 4:1.

The majority of  Oligochaeta identified belonged to the family Tubificidae. The  species identified,

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                                                                                      29
                                        TABLE 2
            Ranges in Values for Chemical Data (mg/l), Lake Winnipeg South Basin,
             1930 and March 1962 to September 1969 (Mean Values in Brackets).
                                       1930 (Bajkov)           March 1962 to September 1969
True Color P* Co Units
Apparent color R Co Units
Turbidity
PH
Calcium
Magnesium
Sodium
Iron
Total hardness
Phosphate (ortho)
Alkalinity
Bicarbonate
Carbonate
Chloride
Carbon dioxide
Dissolved oxygen
B. O. D.
Sulphate
Spec cond jumhos
Total solids
Suspended solids
Dissolved solids
in order  of  occurrence, were Limnodrilus  hoffmeisteri (Cl a parade), Tubifex tubifex (Muller),
Tubifex kessleri (Hrabe) and Limnodrilus udekekiamus (Claparede). A few specimens, tentatively
identifed as  Peloscolex  multisetosus  (Smith) were  obtained. The  other family represented was
Lumbriculidae which constituted less  than one percent of all oligochaetes. The species identified
was Limbriculus variegatus  (Muller).  During some sampling periods, immature forms  comprised
50% of all oligochaetes taken. Identification, based  on number, size and shape of setae, permitted
generic recognition.
-
-
-
'
13.7 to 62.8 (25.2)
2.75 to 33.7 (12.1)
-
0.14 to 1.6 (0.79)
-
-
-
-
28.2 to 128.1 (56.4)
0 to 27.5 (8.4)
-
-
-
3.9 to 118.5 (32.4)
-
100 to 480 (189.3)
-
-
15
20
3
6,60
14.4
0.28
2.0
0.1
41
0
1.8
40
0
1.0
0.1
0
0.4
3
110
38
1.5
74
to 100
to 70
to 130
to 8.99
to 60.0
to 21.9
to 18.8
to 3.9
to 224
to 1.3
to 226
to 176
to 4.8
to 19.8
to 44
to 17.7
to 8.4
to 60
to 580
to 566
to 62
to 374
(30)
(45.5)
(21.7)
(7.79)
(28.3)
(10.5)
(9.4)
(0.79)
(111)
(0.21)
(96.2)
(89.1)
(1.2)
(7.6)
(6.4)
(11.0)
(2.86)
(31.8)
(259)
(173)
(12.8)
(177)

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                                          TABLE 3

          Composition of Benthos, Lake Winnipeg South Basin, March 1962 to September 1969
               (numbers in brackets represent percents of total numbers for that period).
Number of
ivionin
March
Sept.
March
Sept.
March
Sept.2
March
Sept.
March
Sept.
March
Sept.3
March
Sept.
March
Sept.
Mean
1 -
2 =
3 =
4 =
i ear
1962
1962
1963
1963
1964
1964
1965
1965
1966
1966
1967
1967
1968
1968
1969
1969

samples
68
147
42
186
96
150
120
202
60
189
48
99
60
64
57
105

umronomidae .
1053 (61)
835 (48)
576(78)
1057 (15)
1085 (39)
353
207 (10)
3498(43)
396(57)
5889 (74)
620 (66)
748 (45)
1409 (30)
622(13)
1709(17)
1488 (30)
(40)
Includes Trichoptera, Hirudinea,
Peter sen dredge
employed
Cipnemeroptei
288 (17)
184(11)
44(6)
1915(28)
417(15)
713(21)
449(22)
573(7)
79 (11)
779 (10)
28(3)
339(21)
39 (<1)
154(3)
45 «1)
295 (2)
(13)
Anuphipoda,

•a Oligochaeta
263(15)
397 (23)
2(<1)
1153 (17)
1 (<1)
270 (8)
0
786(10)
65(9)
811(10)
176(19)
189(12)
375(8)
1359(27)
2852(29)
1524(31)
(14)
Gastropoda Sphaeriidae Mematoda Others1
29
K<
2(<
1598
1014
1473
1151
2182
(2)
Zl)
CD
(23)
(37)
(44)
(58)
(27)
143(20)
4 (<
:i)
12(1)
133
114
212
518
(8)
(3)
(4)
(5)
522 (11)
(15)

52(3)
208(12)
18(2)
986(14)
213 (9)
523(16)
162(8)
930 (12)
0
329 (4)
89(10)
232 (14)
0
402 (8)
673 (6)
709 (14)
(4)
Unionidae, Chaoborinae, Conchostraca




34(2)
109 (6)
92(12)
112(3)
21 (<1)
26 (<1)
15(2)
109(1)
7(3)
107(2)
15(1)
5 (<1)
2473(54) 190(11)
2196(44) 24 (<1)
4208(42) 19(1)
339(7) 106(5)
(37)4 55
and Nematoda, 1962

Numbers
1719
1734
734
6821
2777
3358
1984
8078
690
7919
940
1646
4600
4969
9924
4983
3312
to 1967.

Numbers
/m*
483
225
332
701
552
315
315
765
224
801
374
318
1464
1468
3225
875
776


Ponar dredge employed
based
on percents from 4 years

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                                                                                      31
The Gastropoda were composed of five families, Physidae, Lymnaeidae, Planorbidae, Valvatidae
and Butimidae.  The genera identified were Physa (Draparnaud),  Aplexa (Fleming), Lymnaea
(Lamarck), Gyraulus (Charpentier), Helisoma (Swainson), Valvata Multer) and Amnicola (Gould
and Haldeman). The genera Amnicola, Physa  and  Valvata together  composed  90% of the
gastropods.

Three  genera,  Sphaerium  (Scopoli),  Musculium  (Link)  and Pisidium  (Pfeiffer)  had  equal
representation among the Sphaeriidae. All Trichoptera were tentatively identified  as the  genus
Limnephilus (Leach) and all Nematoda as the genus Dorylaimus (Dujardin). Members of the family
Unionidae identified were Anodontagrandis (Say), Anodontasp. (Lamarck),Lampsilis siliquoidea
(Barnes), Actinonais  carinata  (Barnes)  and Anodontoides ferusaciana (Lea).  The  Hirudinea
included the species Placobdella  rugosa (Verrill),  Helobdella stagnalis  (Linnaeus), Macrobdella
decora (Say) and Erpobdella (Blainville).

All Conchostraca were identified as Caenestheriella prob. mexicana (Glaus) and the Amphipoda as
Gammarus.  Occasionally, amphipods resembling Pontoporeia were  found (September, 1964).
Their exact identity is in doubt. It is feasible that these were errant migrants from the north basin
displaced by seiche action.

Fish Production

On April 20, 1970, a directive was issued by the Minister of Mines and Natural Resources ordering
closure  of the summer commercial operations on Lake Winnipeg due to mercury contamination.
Mercury levels in excess of the accepted value of 0.5 ppm were found in walleye, northern pike,
sauger and  perch  (Personal communication, Dr. G. Bligh,  Freshwater  Institute,  Winnipeg).
Chloralkali plants outside of Manitoba are believed to be the cause for this contamination.

The commercial fishery of Lake Winnipeg is the largest  in the province of Manitoba in terms of
production, species, value and manpower (Anon., 1969b). Mean annual production from 1931 to
1969 was 13,672,371 pounds (Fig. 3). The major species by catch and  value are sauger,
Stizostedian  canadense (Smith), walleye, Stizostedion vitreum,wh\tef\sh,Coregonusclupeaformis
(Mitchill) and  tulibee  or  cisco,  Coregonus artedii complex. Average annual production for  these
species was 4,494,735, 3,367,026, 2,311,534 and  1,549,578 pounds respectively. Other species
taken are  white perch, Roccus americanus (Gmelin), bullheads, Ictalurus nebulosus (Lesueur),
carp, Cyprinus carpio (Linnaeus), catfish, Ictalurus punctatus (Rafinesque), burbot  or ling. Lota
lota (Linnaeus), pike, Esox lucius  (Linnaeus),  goldeye,  Hiodon alosoides (Rafinesque), perch,
Perca fluviatilis  (Linnaeus), sucker, Catostomus commersoni  (Lacepede), sturgeon, Acipenser
fulvescens {Rafinesque) and trout, primarily rainbow, Salmo gairdneri (Richardson). Since 1961,
there has been a marked decrease in fishing success (Fig. 3).

Hydrographic Data

Mean monthly levels for  Lake Winnipeg, 1930 to 1969,  are shown  in Figure 4. Since 1961, just
prior to the initiation of the present monitoring program, lake levels  were below the 56 year
average. Since 1961, there was  an upward trend in water levels which culminated in the record
level in  1966. At the end of July 1966 the lake was 717.6 feet above M.S.L. This was more than
three feet higher than  the normal for that time of year (Anon., 1969a). The rise continued and on
September 1, 1966 strong north winds  raised the  level  to 721  feet in the south basin (Anon.,
1969a).

-------
 32
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         FIGURE 3   Annual commercial fish production, Lake Winnipeg 1962-1969
                                    OBSERVATIONS

On  the North  American continent.  Lake Erie  is an authenticated  example of a lake whose
environment is deteriorating as a result of pollution (Beeton, 1963; Arnold,  1969). Three indices
of pollution - chemical and physical data, benthic composition and densities, and commercial fish
production - will  be  examined in  Lake Winnipeg and the results compared  with those for Lake
Erie.

Physical and Chemical Data

Major increases  in calcium, magnesium, combined potassium and sodium, sulphate, chlorides and
total solids in Lake Erie  between  1906 and 1958 are well documented (Lewis, 1906; Dole, 1909;
Leverin, 1947; Thomas,  1954; Fish, 1960; Beeton, 1961 and 1963). Turbidity measurements have
been conducted and  increases noted  (Chandler,  1940,  1942a and b, 1944;  Powers et al., 1959;
Fish, 1960;  Kramer,  1961). Evidence supplied by dissolved oxygen determinations supports the
hypothesis of severe  oxygen  depletion over large portions of the  Lake Erie basin (Britt, 1955a;
Wright,  1933;  Powers et al.,  1959;  Fish, 1960; Beeton, 1961 and  1966; Carr, 1962; Thomas,
1963). Beeton (1961) states that there has been a  general warning trend in the waters of  Lake Erie.

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                                                                                      33
Phosphates  and  nitrates  have  been  charged  as  the  major  factors producing  accelerated
eutrophication  in Lake  Erie. Direct measurements,  input rates  and increased levels have been
recorded (Lewis,  1906; Chandler and  Weeks, 1945; Wright,  1933; Curl, 1957; Beeton, 1961;
Kramer, 1961; Matheson, 1962; Verduin, 1964; Harlow, 1966; Ownbey and Kee, 1967).

The only ionic component in Lake Winnipeg showing an increase between 1930 and the period
1962 to 1969 was calcium (Table 2). Values for calcium, iron, chloride and total solids were higher
in 1969 than in 1930 and maximum values for most components were recorded in 1966 and 1967
(Appendix 1). Seichi disc transparencies have declined from one  to two meters  in 1930 to less than
one meter in 1969 (Bajkov, 1930). Due to the shallow depth of the basin and constant mixing by
wind action, no oxygen  depletion results. The variation in chemical concentrations would appear
to be  more  closely correlated with  climatic factors (i.e., precipitation, discharge rates and lake
levels) than  loading rates for pollutants (Fig. 4). The absence of any apparent increases in the
concentrations  of chemical components in  Lake Winnipeg is probably  due to the  length of
residence time and discharge rates. Residence time for Lake Winnipeg has been estimated at from
four to ten  years (Personal communication. Dr. G. Brunskill,  Freshwater  Institute,  Fisheries
Research Board of Canada, Winnipeg). Approximately  30,600 tons of total dissolved solids are
discharged from Lake Winnipeg each day. This value  is based on a mean T.D.S. value of 177 ppm
and a mean flow of 59,200 cfs on the Nelson River.

Benthos

Evidence for the eutrophic nature of Lake  Winnipeg is provided by both chemical data and
benthos (Tables 2 and 4).  Mean standing crop of benthos was calculated as 65.7 ± 3.93 kg/ha.
When this is corrected to deduct the weight of mollusc shells, the value is 58.43 kg/ha. Lakes lying
on the margin of  the Precambrian Shield  have standing crops of from 7.1  to  9.1 kg/ha (Rawson,
1960). Northern oligotrophic lakes have standing crops ranging from 1.6 to 4.7 kg/ha while lakes
south  of the Precambrian Shield normally have standing  crops greater than 9.1 kg/ha  (Table 4).
The standing crop of benthos in Lake Winnipeg more closely approximates values determined by
Lundbeck (1926)  and guarantees its classification as eutrophic. The disparity between values based
on  Bajkov's data (1930) and present calculations could  be indicative of eutrophication. Areas
sampled and the number of samples probably explain the lower values obtained by Slack (1967).
        SO  rtor Mean 1918-1967 • 7I3SZ
   7O9\.
      I93O
                           1940
                                               I95O
                                                                    I960
                                                                                      1969
                                            Y«ar
                 FIGURE 4  Hydrographic data. Lake Winnipeg 1930-1969

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34
The densities of benthos  in  1930 and  the  period  1962 to 1969 provide additional proof of
eutrophication.  Figures based  on Bajkov's (1930) data indicate that benthic densities varied from
437 to 578 organisms/m2. Present data indicates densities of 776 organisms/m2  (Table 3).
In 1930, the amphipods formed from 44% to 85% of total benthic numbers based on certain
stations which correspond to the present sampling program (Bajkov, 1930).  This feature Lake
Winnipeg shared with Lake Athabasca and Great Slave Lake (Larkin, 1948; Rawson, 1953). At
these same stations the mayflies formed 40% and the midge  larvae 6% of total benthic numbers.
Oligochaetes did not contribute significantly to total benthic numbers. The present data indicates
a decline in  amphipod numbers. Decline in both the amphipods and chironomids seems to be
correlated with an increase in both the chironomids and oligochaetes.
The effects of pollutional substances on benthos is manifested by a decline  in the numbers of
species,  a decline in the densities and numbers of those species intolerant of pollution, and a
corresponding increase in the  numbers of those tolerant species (Keup, Ingram and Mackenthun,
1966). Both  the amphipods and mayflies are forms known to be intolerant of pollution; their use
as biological indicators of water quality is recognized (Wright and Tidd, 1933; Campbell, 1939;
                                        TABLE 4
                          Characteristics of Certain Canadian Lakes.
     Lake
Gree1
Wollaston1
Reindeer1
Athababasca2
Great Bear3
Great Slave8
Lac la Ronge1 •*
Amisk
Athapapuskow7 '6
Reed7'6
Winnipeg6
Winnipeg7'6
Falcon7'6
Waskesiu1
He a la Crosse1
Area km2
1,152
2,062
5,569
7,770
28,490
27,200
1,178
321
252
190
23,906
Mean Depth (m)
14.9
20.6
17 +
26.
>100.
62
12.7
13.2
30. 9
-
13.9
 15
 70
446
7.69
11.1
 8.2
 Total Dissolved
T D S ppm Solids
       32
       31
       61
       58
       99
      150
      179
      100

      109
      177

       78
      188
      172
Dry Weight of
Benthos kg/ha
     1.6
     4.7
     1.6
     4.1
     0.5
     2.5
    2.8s
     9.1
  3.4 ± 1.4
  2.4 ±1.0
    44.1
 31.2 ±12.5
  3.6 ±1.5
    24.6
     9.0
1    -   Rawson, 1960
5    =   Oliver, 1960
9    =   approximate
       2    -   Larkin         4    =   Rawson, 1951
       6    =   Bajkov, 1930   8    =   Rawson, 1953
       10  =   Estimated

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                                                                                    35
 Gaufin and Tarzwell, 1952 and 1956; Britt, 1955a and b; Gaufin, 1957 and 1959; Beeton, 1961;
 Leonard,  1962;  Wood,  1963; Beak,  1964; Fremling, 1964; Carr and Hiltunen. 1965; Henson,
 1966; Hiltunen,  1969;  Grimls, 1969; Arnold, 1969). In  the south basin of Lake Winnipeg, the
 amphipods have  declined from a mean value of 65% to less than 1% of total benthic numbers and
 the mayflies from 30%  to 13% between 1930 and the period 1962 to 1969 (Bajkov, 1930; Table
 3). Even more striking is the absence of mayfly nymphs from grid lines A,  B and C (Fig. 2). This
 would seem to mark the point of most northerly penetration of pollutants from the Red River.
 The Oligochaeta, particularly members of the family Tubificidae,  are known to thrive under
 conditions of organic enrichment commonly encountered in polluted environments. Oligochaete
 densities and species representation have been used as indices of pollution (Wright, 1933; Britt,
 1955a and b; Beeton,  1961; Carr and Hiltunen, 1963; Henson, 1966; Johnson and Matheson,
 1968; Hiltunen,  1969).  Oligochaete densities in  the  south basin of Lake Winnipeg are normally
 larger than the 1400/m2 along the A grid line  and decrease to 275/m2 along the B grid line  (Fig.
 2). Using Wright's system (1933), the density  of 1400/m2  would  be indicative of moderate
 pollution.
 Approximately 95% to 98% of all oligochaetes  in the south basin of Lake Winnipeg were the
                                   TABLE 4 (Cont'd)
                         Characteristics of Certain Canadian Lakes.
    Lake
Gree1
Wollaston1
Reindeer *
Athabasca2

Great Bear3

Great Slave3
Lac la Ronge1'4
Arnisk1
Athapapuskow7 '6
Reed7'6
Winnipeg6
Winnipeg7 '6

Falcon7'6
Waskesiu1
De a la Crosse1
Major Benthic Groups
  Chironomidae
  Amphipoda
  Amphipoda
  Amphipoda and
   Chironomidae
  Mollusca

  Amphipoda
  Chironomidae
  Amphipoda
  Amphipoda
  Chironomidae
  Amphipoda
  Amphipoda and
   Epnemeroptera
  Chironomidae
  Chironomidae
  Chironomidae,
   Amphipoda and
   Sphaenidae
 Geology of Basin
 Precambrian
 Precambrian
 Precambrian

 Precambrian
 Precambrian and
  Paleozoic
 Precambrian
 Precambrian
 Precambrian
 Precambrian
 Precambrian
 Precambrian

 Precambrian
 Precambriam
Paleozoic

Paleozoic
Flushing Time (Years)

        14
        11
        19
        3
    4 toll 10
                                                                           0.75

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 36


species Limnodrilus hoffmeisteri (Claparede),Li'mnodri/ussp. and Tubifex tub if ex (Muller). These
commonly occur in polluted zones (Johnson and Matheson, 1968; Hiltunen, 1969).

The  last group of  benthic organisms commonly occurring  in Lake Winnipeg  and  known to  be
pollution-tolerant is the Chironomidae (Britt, 1955a and b; Beeton, 1960 and 1961; Wood, 1963;
Carr and Hiltunen, 1965; Keup, Ingram and Mackenthun,  1965; Hiltunen, 1969). Brenniman,
Soyak  and  Curry  (in press)  have  classified chironomic  species according  to water quality
preference.  This method was adopted and modified for use in Lake Winnipeg. All species of the
genera  Chironomus, Chironomus (Kiefferulus), Chironomus (Einfeldia) and Glyptotendis were
classified as "pollutional". The  genera Pentaneura, Polypedilum, Harnischia, Calopsectra and
Cryptochironomus  were classified as cosmopolitan  and the remainder of the species as "others",
i.e.. their water quality preference is unknown. No species classified as "clean water" by Curry
were identified in Lake Winnipeg: There is a distinct possibility that species classified as "others"
may, in reality, be clean water forms. However, our data indicates that 39% of the chironomids
could be classified as "pollutional".

The trophic level for Lake Winnipeg  was tentatively determined as 1.5 (Brinkhurst,  Hamilton and
Herrington, 1968). This is less than that determined  for western lake Erie (2.0).
                                       TABLE 5

Classification of Chironomidae According to Water Quality Preference, Lake Winnipeg South Basin,
September 1962 to September 1969 (values are percents of total chironomid numbers for that period)

Year              Month              Pollutional            Cosmopolitan            Others

1962            September                54                    25                  20

1963            March                    34                    46                  20
                September                26                    53                  21

1964            March                    17                    71                  12
                September                79                    14                   7
1965            March                    4                     66                  30
                September                43                    44                  13

1966            March                    26                    44                  30
                September                66                    20                  14

1967            March                    43                    45                  12
                September                55                    31                  14

1968            March                    27                    67                   6
                September                22                    42                  36

1969            March                    44                    48                   8
                September                40                    50                  10

Mean                                     39                    44                  17

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                                                                                     37
In conclusion, it is evident by changes in the benthic composition, that Lake Winnipeg has been
subjected to eutrophication believed  to be the result of pollution. These changes are similar to
those which have  occurred in Lake  Erie and  which are  presently occurring in Lake  Michigan
(Powers and  Robertson,  1965; and  Robertson and Alley,  1966). The first change in benthic
composition was a shift from Amphipoda to Chironomidae. Ultimately the benthic population will
be dominated by the Oligochaeta.

Fish Production

It has been noted that the annual commercial fish production in Lake Winnipeg declined in 1961
and has since remained at levels below the 38-year average (Fig. 3). Overfishing and the use of
illegal  mesh  nets  were  believed  to  be the  major factors  producing the decline  (Personal
communication, Mr.  W. Pollard, Manitoba  Department of  Mines and Natural  Resources). The
closure of commercial fishing operations on Lake Winnipeg may  permit some  recovery of fish
stocks.

Hydrographic Data

Since 1961, there  has been an  increase in Lake Winnipeg water levels terminating in  the 1966
maximum (Fig. 4). Increased precipitation and heavy run-off combined to produce high lake levels
accompanied  by high chemical concentrations (Table 2). Increased nutrient loading produced high
benthic densities  (Table  3). Benthic densities more  than four  times greater than the value of
801/m2 in September 1966 have been subsequently  recorded. While  population increases could
have occurred, the concentration method cannot be overlooked as a causative agent.

                            SUMMARY  AND CONCLUSIONS

Between March 1962 and September 1969, surveys on the south basin  of  Lake Winnipeg were
conducted twice yearly. The purpose of these surveys was to determine changes within the basin
attributable  to pollution. Emphasis was directed to the chemical composition of water and
densities and composition of the benthos.

The only ionic component showing an increase since 1930 is calcium.  Mean concentrations of
calcium,  iron, sulphate and total solids were higher in 1969 than in  1930.  Maximum  levels for
most chemical components were recorded in 1966 and  1967, corresponding to high lake water
levels. The lack of any significant increases in concentrations is believed to be due to low residence
time and effective flushing rates.

Since 1930, benthic densities have increased from values of 437 and 578/m2 to 776/m2 during the
1962-1969 period. The  composition  of  the benthos  has shifted  from  that dominated by
Amphipoda and Ephemeroptera in 1930 to the  present Chironomidae - Oligochaeta configuration.
Approximately 39% of all chironomids and 95% of all oligochaetes, between 1962 and 1969, were
composed of  species which could be termed pollutional. As enrichment proceeds, the benthos in
the south basin of Lake Winnipeg will ultimately be dominated by oligochaetes.

                                 ACKNOWLEDGMENTS

Since its inception in 1962,  numerous persons have contributed to the pollution  monitoring

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38


program on  Lake Winnipeg. To all, I  should  like to extend  my appreciation  and thanks. I  am
grateful to Dr.  K. H. Doan, Director  of Research, Manitoba Department of Mines and Natural
Resources for advocating the preparation of this manuscript and to Dr. F. J. Ward, Professor,
Department of Zoology, University of Manitoba for his constructive criticism.
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Matheson, D. H. (1962) A pollution study of western Lake Erie, Inst. Sci. Tech., Univ. Mich. Pub.
     No. 9:15.

Matheson, D. H. (1965) A pollution study of western Lake Ontario, Proc. Great Lakes Res. Div.,
     Univ. Mich. Pub. No. 9:15-20.

Minder,  L.  (1926)  Biologische-chemische  Untersuchungen  im Zurichsee,  Rev. d'Hydrologie,
     3:1-69.

Miller,  R. B. (1947) Great Bear Lake, Bull. Fish. Res. Bd. Canada, 72:31-44.

Neave,  F. (1932) A Study of  the May Flies  (Hexagenia) of Lake Winnipeg, Contributions to
     Canadian Biology and Fisheries, Vol. VII, No. 15 (Series A, General, No. 12):179-201.

Northcote, T. C. and Larkin, P. A.  (1963) Western Canada, Chapter 16,  p. 451-485,  In Limnology
     in North America, D. C. Frey, Editor, Univ. Wis. Press, Madison, Wis.

Oliver,  D. R. (1960) The  macroscopic  bottom fauna of Lac la Ronge. Saskatchewan, J. Fish. Res.
     Bd. Canada, 17(5) :607-624.

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                                                                                    43
Ownbey, C. R. and  Kee,  D. A. (1967) Chlorides in Lake Erie,  Proc. Great Lakes Res. Conf.
     10:382-389.

Powers, C. F., Jones, D. L., Mundinger, P. C. and Ayers, J. C. (1959) Exploration of collateral data
     potentially applicable  to Great Lakes hydrography and fisheries, Final Rept., Phase II, U. S.
     Fish and Wildlife Serv., Contract No. 14-19-008-9381, Great Lakes Res. Inst., Univ. Mich.,
     164 p.

Powers, C. F. and Robertson, A. (1965) Some quantitative aspects of the macro-benthos of Lake
     Michigan, Great Lakes Res. Div., Univ. Mich. Publ., 13:153-159.

Powers, C. F. and Robertson, A. (1966) The aging Great Lakes, Sci. Amer., Nov. 1966:94-100.

Rawson, D. S. (1951) The total mineral content of lake waters. Ecology, 32(4):669-672.

Rawson, D. S. (1953) The bottom fauna of Great Slave Lake, J. Fish. Res. Bd. Canada, Volume X,
     No. 8:486-520.

Rawson, D. S. (1960) A limnological comparison of twelve large lakes in northern Saskatchewan,
     Limnol. Oceanogr., 5(2): 195-211.

Roback, S. S.  (1957) The  immature tendipedids of the Philadelphia area, Monog. Acad. Nat. Sci.
     Philadelphia. No. 9, 152 p.

Robertson, A. and Alley,  W. P. (1966) A comparative study of  Lake Michigan macrobenthos,
     Limnol. Oceanogr., 11 (4):576-583.

Slack,  H. D. (1965) The profundal fauna of Loch Lomond, Scotland, Proc. Ray. Soc., Edinburgh
     B, 69:272-297.

Slack,  H. D. (1967) A brief survey of the profundai benthic fauna of lakes in Manitoba,  J. Fish.
     Res. Bd. Canada 24(5): 1017-1033.

Thomas, J. F.  J. (1954) Industrial water resources of  Canada, Upper St. Lawrence River -Central
     Great  Lakes drainage basin in Canada, Dept. Mines Tech. Serv., Water Surv. Rept. No. 3,
     Mines Br. Rept. No. 837, 212 p.

Thomas, N. A. (1963) Oxygen deficit rates for the central basin of Lake Erie, Great Lakes Res.
     Div. Univ. Mich., Pub. 10:133.

Townes, H. K. Jr. (1945) The nearctic species of tendipedini (diptera, tendipedidae-chironomidae),
     Amer. Mid. Nat., Vol.  34, No. 1,266 p.

Wand,  P.  (1966)  Lake Winnipeg water  drops-damage rises, Winnipeg Free Press, September 6,
     1966.

Verduin, J.  (1964)  Changes in western  Lake Erie during the period  1948  - 1962, Verh.  Int.
     Verein., Limnol., XV:639-644.

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 44
Ward, B. W. and Whipple, G. C. (1959) Freshwater Biology, 2nd Edition, John Wiley and Sons,
     New York, 1248 p.

Wood, K. C. (1963) The bottom fauna of western Lake Erie, Great Lakes Res. Div., Univ. Mich.,
     10:259-265.

Wright,  S. (1933) Limnological survey of western Lake Erie, Special Scientific Report Fisheries
     No. 139, U. S. Dept. Fish and Wildlife, 341 p.

Wright,  S. and Tidd, W. (1933) Summary of limnological investigations in western Lake Erie in
     1929 and 1930, Trans. Amer. Fish. Soc., 63:271-285.

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                                                   APPENDIX 1

                     Ranges in Values for Chemical Data (mg/l). Lake Winnipeg South Basin, March 1962
 Physical and
Chemical Factors

True color P+ Co units
    1962                  1963
March   September   March     September
      1964
March     September
      1965
March     September
Apparent color P+ Co units 20 to 50
(35.6)
Turbidity
pH
Calcium
Magnesium
Sodium
Iron
Total hardness
Phosphate (ortho)
Alkalinity
Bicarbonate
Carbonate
Chloride
Carbon dioxide
Dissolved oxygen
B. O. D.
Sulphate
Spec. cond. jU mhos
Totat solids
Suspended solids
Dissolved solids
Number of samples
1.0 to 30
(10.8)
7.0 to 7,8
(7.3)
16.8 to 94.4
(26.3)
-

0.6 to 3. 9
(0.4)
54 to 382
(96.7)
-
18 to 158
(34.4)
•
•
2.0 to 20.4
(6.8)
4.6 to 732
(9.5)
6.5 to 16.9
(13.7)
*w
•
-
38 to 650
(161)

•

40 to 70
(52.5)
4.5 to 34
(15.1)
7.2 to 8.4 6.7 to 7.6
(7.6) (7.3)
16.0 to 40.0
(23.9)
-
-
0.1 to 1.08
(0.5)
54 to 160
(91.3)
-
92 to 226 40 to 194
(144) (99.8)
-
-
2.0 to 13.5
(5.6)
4,0 to 44 1.7 to 6.8
(13.7) (3.2)
8.2 to 11.29.6 to 17.1
(9.4) (13.1)
2. 9 to 8.4
(4.9)
-
-
94 to 284
(56)
1.5 to 27
(10.4)
-
22
-
-
6.6 to 7. 6
(7.2)
14.4 to 36.8
(28.9)
3.9 to 13.6
(10.2)
2.5 to 13.5
(8.2)
0.3 to 2.3
(0.8)
52 to 148
(115)
-
44 to 122
(89.5)
53 to 132
(106)
0 to 4.8
(1.2)
1.0 to 11.0
(6.5)
x
9.2 to 9.8
(9.5)
0.5 to 1.4
(0.9)
8.2 to 40.4
(28.3)

106 to 238
(190)
-
82.0 to 309.9
(189)
24
30 to 60
(48.5)
4.0 to 32.5
(17.1)
6.7 to 8.0
(7.2)
15.2 to 36.0
(25.2)


0.12 to 0.68
(0.34)
54 to 126
(99.6)
•
40 to 181
(104.4)


1.5 to 100
(5.6)
0 to 20.4
(3.9)
3.2 to 17.7
(12.1)
0.4 to 6.3
(3.1)
-

80 to 210
(148)
1.0 to 9.0
(3.9)

32
-
-
7.2 to 8.1
(7.7)
14.4 to 60.0
(25.0)
4.9 to 12.2
(9.0)
2.0 to 9.5
(6.4)
1.4 to 3.9
(2.3)
56 to 122
(94.2)

48 to 94
(75.3)
58 tollS
(91.3)

1.2 to 10.0
(5.9)
-

-
11.6 to 37.8
(28.3)
-
110 to 286
(214)

•
18
"
6 to 20
(10.3)
7.4 to 8.2
(7-8)
0.8 to 36.0
(28)
-

-
66 to 140
(105.8)
-
52 to 116
(87.7)
-
'
2.0 to 13.5
(6.7)
-
8.0 to 17.5
(13.9)
2.0 to 4.1
(3.3)
-
-
102 to 368
(164)
0 to 37
(14.4)

39

-
7.5 to 7.9
(7.6)
22.0 to 32.8
(26.4)
1.7 to 12.6
(9.3)
4.5 to 11.5
(7.6)
0.36 to 1.4
(0.73)
41 to 134
(104)
0.11 to 0.40
(0.21)
40 to 98
(77)
40 to 110
(94.3)
'
4.0 to 11.5
(8.5)

-

28.1 to 49.5
(38.8)
-
150 to 216
(173)


8
                                                                                                                                  -p.
                                                                                                                                  01

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                          APPENDIX 1 (cont'd)
Ranges in Values for Chemical Data (mg/l). Lake Winnipeg South Basin, March 1962
Physical and
Chemical Factors
True color P+ Co units
1966
March September
1967
March September
15 to 25
(19)
1968
March September
15 to 45
(25)
191
March
30 to 40
(36)
59
September
30 to 100
(42)
Apparent color P+ Co units ..-•--•
Turbidity
PH
Calcium
Magnesium
Sodium
Iron
Total hardness
Phosphate (ortho)
Alkalinity
Bicarbonate
Carbonate
Chloride
Carbon dioxide
Dissolved oxygen
B. O. D.
Sulphate
Spec, cond, M mnos
Total solids
Suspended solids
Dissolved solids
Number of samples
-
7.3 to 7.7
(7.5)
14.4 to 36.8
(22.4)
2.9 to 12.6
(7.0)
2.0 to 13.0
(5.2)
0.14 to 0.32
(0.2)
48 to 144
(85.2)
0.11 to 0.22
(0.14)
WP
48.8^129
-
0 to 12
(4.3)

10.2 to 16.5
(14.4)
-
17 to 48
(28)
-
82 to 212
(132)
-
74 to 208
(127)
20
9 to 50
(26)
7.9 to 8.0
(8.0)
17.6 to 44.2
(33.7)
10.9 to 18.7
(14.2)
9.5 to 17.8
(13.3)
0.11 to 1.8
(0.98)
118 to 188
(151)
0.34 to 1.3
(0.53)
90to3139
110 to 170
(138)

0.2 to 13.4
(5.4)
-
7.7 to 10.0
(9.0)
-
16.5 to 58.4
(365)
-
160 to 280
(211)

96 to 276
(183)
8
50
T.8
59.2
32'.1
26.4
14.2
280
0.39
182
222

19

10.0 to 16.
(13.5)
-
45.3
-
642

338
1
4 to 130
(38)
7.4 to 8.2
(7.8)
27.2 to 48.0
(36.2)
9.7 to 21.9
(13.8)
8.6 to 18.8
(11.4)
0.04 to 1.63
(0.44)
112 to 240
(147)
-
-
•
-
11.5 to 19.8
(15.7)
-
,3 7.3 to 10.6
(8.7)

28.2 to 60.0
(41.8)
-
170 to 346
(206)
4 to 64
(14)
158 to 304
(203)
34
15 to 55
(31)
7.98 to 8.11
(8.07)
30.4 to 38.4
(33.2)
7.3 to 12.6
(10.8)
8.3 to 13.0
(10.4)
°-W'7
110 to 144
(126)
0.05 to 0.11
(0.08)
82 to 120
(98)
100 to 146
(119)
-
9.1 to 13.3
(11.0)
4 to 10
(7.3)
0.0 to 10.1
(7.1)
-
28.8 to 41. 2
(35.1)
195 to 290
(229)
-

•
20
5 to 60
(18)
7.33 to 8.20
(7.83)
17.6 to 49.6
(30.0)
0.28 to 19.4
(9.3)
3.2 to 17.6
(9-7)
0.14 to 3.12
(0.59)
57 to 196
(113)
0.0 to 0.36
(0.13)
44 to 144
(86)
53 to 176
(105)

2.5 to 18.0
(8.8)
•
9.8 to 10.4
(9.9)
-
3 to 60
(34)
-
9.0 to 326
(180)
0 to 50
(15)
80 to 290
(160)
32
3 to 30
(16)
"f^7)-72
27.2 to 31. 2
(28.0)
8.9 to 11.2
(9.9)
9.3 to 12.0
(10.1)
0.16 to 1.04
(0.28)
105 to 122
(110)
0.13 to 0.27
(0.17)
76 to 88
(83)
93 to 107
(100)

7,0 to 8.0
(7.3)
1.9 to 32.4
(7.2)
4.5 to 16.0
(12.2)
-
24.7 to 31.3
(29.4)
235 to 270
(252)
150 to 202
(175)
0 to 52
(10)
146 to 180
(165)

10 to 320
(35)
7. 65 to 8.99
(7.98)
12.8 to 52.0
(29.0)
2.9 to 22.8
(11.1)
2.7 to 35.3
(12.1)
0.20 to 7.0
(1.31)
48 to 224
(116)
0.085 toO.44
44t02168
54 to 205
(114)
"
1.5 to 22.8
(8.8)
0.1 to 1.5
(0.3)
8.3 to 9.6
(8.7)
0.4 to 2.3
(1.3)
3.6 to 8.2
(4.0)
110 to 580
(298)
98 to 566
(246)
6 to 62
(22)
92 to 374
(212)
33

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                                                                                                     47
                                     APPENDIX 2
                          Larval Forms of Chironomidae Collected
Subfamily Tenypodinae
Tanypus sp.
Procladius sp.
Procladius riparius (Malloch)
Procladius culiciformis (Linnaeus)
Procladius nr. adumbratus (Johannsen)
Coelotanypus sp. (Kieffer)
*Clinotanypus sp. (Kieffer)
•Zavrelimyio sp.
Peritoneum cornea (Fabricius)
Ablabesmyia sp.

Subfamily Diamesinae
*Diamesa sp.

Subfamily Orthocladiinae
•Canliocladius sp. (Kieffer)
'Heterotrissocladius sp.
*Nanocladius sp.
*Orthocladius sp.
*Psectrocladius sp. (Kieffer)
•Trichocladius sp. (Kieffer)
Subfamily Chironominae

Chironomus sp.
Chironomus attenuates (Walker)
Chironomus riparius (Meigen)
Chironomus plumosus (Linnaeus)
Chironomus tentans (Fabricius)
Chironomus tuxis (Curran)
Chironomus staegeri (Lundbeck)
Chironomus anthracinus (Zetterstedt)
*Chironomus neomodestus (Malloch)
*Chironomus tendipediformu (Goetghebuer)
'Chironomuspaganus (Meigen)
^Chironomus hyperboreus (Staeger)
*Chironomus ochreatus (Townes)
Chironomus (Kiefferulus)
Chironomus (Einfeldia)
Microtendipes sp.
Glyptotendipes sp. (Kieffer)
Cryptochironomus digiiatus (Malloch)
Cryptockironomus fulvus (Johannson)
Polypedilum (Tripodura) scalaenum (Schrank)
Chironomus (Cryptochironomus) nais
Cryptochironomus (Hamischia)
Ttmytarsus (Vander Wulp) = Calopsectra (Kieffer)
Hamischia (Kieffer)
 Reference

 Mason, 1968
 Roback, 1957
Mason, 1968
Mason, 1968
Mason, 1968
Curry, 1962
Mason, 1968

Curry, 1962

Roback, 1957


Mason, 1968


Roback, 1957
 *  The identity of these genera and species is in doubt. Few specimens were obtained and all were
 larvae.

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        EUTROPHICATION  IN  SOME  LAKES AND  COASTAL  AREAS
    IN  FINLAND, WITH SPECIAL REFERENCE TO POLYHUMIC  LAKES
                                 Pasi O. Lehmusluoto
                                  INTRODUCTION

The dominant feature of the Finnish inshore waters is the fact that the lakes are linked together by
short stretches of running water. They form in this way watercourses (Fig. 1). The number of lakes
is estimated to be within the range of 55,000 • 75,000. Their total area is 32,000 km2 and water
volume is about  220 km3 (mean depth about 7 meters). The mean run-off (MQ) is 95 km3/year.
The average color of the water is comparatively high in  the whole country, i.e. 91 mg Pt/l. This
means that the average hurnus content of the water is about 13 mg humus (dry weight)  per liter
(Ryhanen, 1968). The iron content is also comparatively high, and  averages  1.1 mg/l. The lake
water  is normally clear, slightly acid (pH 6.6), and the conductivity  is low, under 70 micromhos
(Laaksonen, 1970).
                           25 E
                                             27'E
                                                               29 E
      61 N
                                                                            61 N
                           25-E
                                              27 E
                                                                 29 E
              FIGURE 1  A part of the Finnish lake district. S=Lake Saimaa.
    This investigation was supported in part by the National Research Council for sciences in
Finland, in part by the Foundation for Research of Natural Resources in Finland and in part by
the City of Helsinski.
                                         48

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                                                                                       49
Allotrophic  humus, and  organic  matter  produced  in autotrophic  phytoplankton  primary
production, especially in  connection with eutrophication, have been found to be most important
factors in protection of  polyhumic lakes in maintaining sufficient oxygen concentration in the
water bodies  (Ryhanen,  1968). In certain areas carbon rich pulp mill effluents may also play an
important role in loading  the waters.

The  lakes in  Finland  are normally  dimictic. The  spring circulation  is not,  however, always
complete in small lakes. The ice period lasts on the lakes for 150 - 250 days, making the conditions
in the water more favorable for decomposition than for phytoplankton primary production. In the
hypolimnion  the  oxygen consumption caused  by different kinds of oxidation processes (e.g. the
decomposition of organic material produced in  primary production, the decomposition of pulp
mill effluents, and ferrous iron oxidation)  may be great, and lead to an oxygen  deficit during
winter  and summer stagnations. This is especially severe during summer stagnations, when the
preceding spring circulation has not been complete.

Increase in phytoplankton primary production is perhaps not as important in polyhumic lakes as
in the nonhumic lakes. This is due to the "inhibitive" effect  of humus to the total  daily
phytoplankton primary production (Shapiro,  1957). This effect is caused mainly by the strong
light absorption of humic material. In algal assay bottle tests in constant light, humus has shown to
be slightly biostimulative  (Demmerle,  1967). The visible light (E 400  - 700 nm)  penetrates
polyhumic lakes only 2-3 meters (Fig. 2). Humus alone depresses the trophogenic layer beyond the
normal properties of the water. Thus in polyhumic water bodies there is produced daily only a
part of that phytoplankton material produced in similar nonhumic waters.
                                       MG C/M3/ DAY - %
                                    I     10    IOO   IOOO  IOOOO
                                              EUTROPHK
                                   10    IOO I    IO    100 I
                             I
                             2
                             3-

                             i-
                            to-
                           20
                               OLK30TROPHC
                               POLYHUMIC
                                OLIGOTROPHIC
                                NON-HUMIC
                                                          10    IOO
OLIGOTROPHIC
'BLUE LAKE"
FIGURE 2
Phytoplankton primary  production (mg C/m3/day, solid  line) and visible light
extinction (%, dashed line) vs. depth in different kinds of waters in the middle of the
growing season.  Data for the oiigotrophic "blue lake" is from Rodhe et al. (1966).
Phytoplankton production and light extinction are in logarithmic scale.

-------
 50
In some clear water lakes, so called "blue waters", where the optical purity of the water is great
(Fig.  2),  the  effect  of ultraviolet radiation  can cause  a  reverse  vertical  distribution of
phytoplankton  primary  production  (Rodhe et al.,  1966). Ultraviolet radiation depresses this
production below its  potential  capacity because phytoplankton production can proceed only in
the layers where the  influence  of  ultraviolet radiation  is negligible and there is still visible light
illumination. In these  lakes this layer is often beyond the optimum visible light layer in the lower
epilimnion (Rodhe et al.,  1966).

Normally in nonhumic and nonturbid lakes increasing phytoplankton mass causes the trophogenic
layer to be depressed, and the maximum phytoplankton primary production per cubic meter (in
optimum visible light layer) is moved closer to the water surface. In polyhumic and very turbid
lakes this does not happen because of the already thin trophogenic layer (Fig. 2).

In Finnish  lakes, as in some mountain lakes of Austria (Pechlaner, 1964), high phytoplankton
primary  production   beneath  the  ice during  spring  time normally  cannot  be   found.  The
phytoplankton primary production is at that time barely measurable. The lack of an under-ice
spring bloom may be partly due to  the relatively fast ice melting, as the ice does not remain on the
water long enough after the  snow has melted to allow sufficient light for intensive phytoplankton
production.  Low rates of primary production  can be measured under ice normally during early
winter before the ice is covered with snow (Pechlaner,  1964).

In Alaska almost half  of the annual phytoplankton primary production may occur beneath the ice
sheet in  spring  time, e.g.  Lake  Schrader and Lake  Peters  (Hobbie,  1964).  The  highest
phytoplankton production for the  whole year in Lake Schrader  was also found in spring under the
ice. Rodhe et al. (1966) measured considerable under-ice phytoplankton  production in Swedish
Lapland. The high under-ice production in the two Alaskan lakes in spring time was a result of the
relative lack of turbulence in the water beneath the ice. The algae remained in the euphotic zone
continuously during  ice  period. After the ice had  left and  the lakes began  to circulate,  the
phytoplankton primary production dropped sharply. In Finnish lakes the phytoplankton primary
production usually increases sharply during this period.  At this time of year the algae can stay in
the euphotic zone only a small part of their lives, as in  polyhumic lakes during summer time. These
algae also appear to be adapted to low light intensities (Hobbie, 1964).

The growing season is short in Finland with daylight in June averaging 18 hours, August 16 hours,
but in October only 10 hours. The ice period normally lasts from November to April.

The vernal diatom bloom is dependent on the length of the day and on the illumination during the
day (Gran,  1929). This bloom can  be normally found in the Finnish waters from the end of April
to the end of May, when the solar radiation exceeds 2.5 - 3.5 kcal/m2/min. The vernal diatom
bloom could possibly be found when the solar radiation exceeds 1.5 kcal/m2/min (Smayda, 1959),
but the bloom is hindered at that time by the  ice cover (Lehmusluoto, 1968).

During summer time  in  polyhumic  lakes, the  lack  of light-and in  some Alaskan  and Swedish
mountain lakes, the overwhelming light (Hobbie, 1964, Rodhe et al., 1966) seems to limit the
total daily primary production  per square meter  of  the water, but  the nutrients may limit the
maximum primary production of a cubic meter of water  (Hobbie, 1964).

When discussing primary production, one cannot help dealing with the lake  typology. Nowadays it

-------
                                                                                      51
has been suggested that primary production could be the basis for the trophic classification of
waters (Rodhe, 1958, 1969, Findenegg, 1964). There are many parameters of primary production
that could be used: 1) the shape of the primary production curve {Findenegg, 1964), 2) primary
production per square unit (diurnal, annual)  (Rodhe,  1958, Findenegg,  1964, Hubel, 1968), 3)
maximum primary production  per unit volume (Rodhe, 1958, Lehmusluoto,  1969) 4) so called
V/0-quotient as suggested by Rodhe (1958).

I  would like to suggest that the mean maximum primary production rate per unit volume in the
water column during the growing season measured in situ, or in constant light, could be used as an
index for many  kinds  of  water bodies.  This would give a relative but objective index for the
phototrophic level of the water. It would not reflect the total amount of organic material built up
in the whole water column (which can be estimated by the light extinction curve), but it might be
informative about the degree of eutrophication of the water. No suggestions for the designation of
oligotrophic or eutrophic waters are presented, because the data available is insufficient.

When talking about lake typology, especially of polyhumic waters,  it may be appropriate  to use
phytoplankton primary  production  only  as  a measure of the autotrophic state. The  direct
comparison of trophic states of humic and nonhumic lakes is impossible, as the classification of
polyhumic  lakes on  the basis of  phytoplankton  production cannot give an objective result
(Ryhanen, 1968). Ohie (1940,  1956) has suggested that also the  heterotrophic state should be
taken into account.

                           EXAMPLES OF EUTROPHICATION

Experiments with Polyhumic Water

In order to get some information about the role of nitrate nitrogen and phosphate phosphorus in
the eutrophication process of polyhumic  waters, a  series  of preliminary tests were made by algal
assay bottle tests (Bringmann and Kuhn,  1956; Skulberg, 1964), with water from the polyhumic
Lake Hakojarvi (61° 15' N, 25° 12' E). The color of the water was about 150 mg Pt/l and the iron
content averaged in the whole water  column (maximum depth 15 meters)  about 0.5 mg/l. The ice
period lasts on this lake about  180 days, from November to the end of April. Spring circulation
was complete during 1966 - 1970 only twice.

Results showed that  nitrogen  was the primary limiting nutrient. Nitrogen was also a limiting
nutrient for bacterial growth in  this water (Sederholm, 1969). When nitrogen and phosphorus were
added together a large algal growth occurred (Fig. 3).

A series of experiments on phytoplankton  primary production during  1968-1969 using 7 in situ
plastic test cells were conducted. The cells were 10 meters deep, 1.2 meters in diameter, and the
top was open (Goldman, 1962). The water volume was about 12 m3. Only the results of the test
cells of 1968 are dealt with in this paper, as the results of 1969 were quite similar in nature.

Nitrate  nitrogen  and  phosphate phosphorus were added  to  the  test  cells according to  the
preliminary tests by algal assay  in bottles. Nutrient additions varied from 0.05 to 1.0 mg/l nitrogen
and 0.005 - 0.1 mg/l phosphorus. The nutrient additions to the different test cells are shown in
Table 1.

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 52
                                                  AU3AL ASSAY
                                                  CELLS/LITER
                                                      rSIO10
                                                       - 4-I010
                                                         10'°
                                                  I MS m_ (ADDED)
FIGURE 3  The influence of different nitrogen (nitrate) and phosphorus (phosphate) additions in
            polyhumic lake water (Lake Hakojarvi) as measured by algal assay in bottles. Test
            alga was Chlorella sp.
CeD No.

NO3-N,mg/l

PO4-P,mg/l
            TABLE  1

Nutrient Additions into the Test Cells

    1234         5        67

             1.0        -        1.0       0.5       0.1      0.05

                      0.1       0.1      0.05      0.01     0.005
Phytoplankton  primary production, which was measured  by the carbon-14 method (Steemann
Nielsen, 1952), was made eleven times during the test period, (17.7. - 8.10. 1968). The test period
was about 2/3 of the whole growing season. The background production (Cell No. 1) was 1.58 g
C/m2/test period  (average  for  test period 20.2 mg C/m3  (max.)/day). In Lake  Hakojarvi  in
1966-1969 the phytoplankton primary  production averaged 2.66 g C/m2 /growing season (average
for test period  17.7 mg C/m3  (max.)/day). There were not any large changes in phytoplankton
production in the test cell, where only nitrogen had been  added, but phosphorus addition alone
caused a slight increase (Table 2). Phosphorus did not alone cause significant eutrophication, i.e.
phosphatetrophication  (Thomas, 1968). In the cells where both nitrogen  and  phosphorus were
added the increase  in phytoplankton production was greater with greater .additions of nutrients.
The highest value. 8.16 g C/m2/test period (154.2 mg C/m3 (max)/day in test period), was in the
cell containing the greatest nutrient addition (1.0 mg N/l and 0.1 mg P/l).

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                                                                                      53
1
1.58
29.2
2
1.32
23.5
3
1.42
44.1
4
8.16
154.2
5
3.48
65.3
6
2.80
49.6
7
1.92
51.5
                                        TABLE  2

        Phytoplankton Primary Production g C/m2/test period and mg C/m3 (max.)/day
             on the Average in the Test Period For Nutrient Additions See Table 1

 Cell No.

 g C/m2 /test period

 mgC/m3 (max.)/day*

 * Average for the growing season (eleven measurements).
 The oxygen stratification in the different test cells did  not show any great variations. In the
 epilimnion at a depth of 1 meter each cell contained a range of 8.3 to 8.9 mg Oj/l, and at 5 meters
 depth from  6.8 to 7.1 mg O2/l. in the hypolimnion at 10 meters depth between 5.7 to 6.2 mg
 02/l. The highest oxygen values in the epilimnion were normally found  in the cells where  both
 nitrogen  and phosphorus had been  added.  However, the  lowest values in  hypolimnion were not
 found in these cells. Nutrient additions in these experiments  apparently did not stimulate oxygen
 consumption in the hypolimnion.
The uptake of radioactive glucose by heterotrophic bacteria (Wright and Hobbie, 1965) was also
stimulated  by nitrogen and phosphorus.  In  the test  cell  where the greatest nitrogen and
phosphorus addition was made, primary production increased about five times, and the uptake of
radioactive  glucose  increased about  ten times (Leppanen, 1970). The bulk of heterotrophic
bacteria which caused the  uptake of radioactive glucose may have been dependent on the algal
mass produced, because the increase of  glucose uptake occurred only in the upper epilimnion
where primary production  was at a maximum (Fonden, 1969). The same nutrient addition was
present both in the lower epilimnion and in hypolimnion.

Although it seems that the humus in  the water did not in these experiments form so serious a
problem in maintaining sufficient oxygen concentration  in hypolimnion as the  organic material
built up by  the  phytoplankton primary production,  humus  may be important in the total
production of polyhumic waters.  The zooplankton and fish production in the Finnish polyhumic
lakes seem to be greater than the phytoplankton primary production can yield (Ryhanen, 1968).
It is proposed that humus as such, or transformed to bacterial biomass, may serve as food for the
zooplankton (Jarnefelt,  1956), and thus lead to a relatively high fish production. It has been
shown  that the bacterial numbers in  humic waters are  normally  comparable to the numbers in
eutrophic lakes (McCoy and Sarles, 1969).

On March 22, 1970 the entire Lake Hakojarvi was fertilized by adding 750,000 m3 phosphorus
and nitrogen to bring the lake water concentration up by 1 mg  N/l and 0.1 mg P/l. Results from
this experiment are not yet  available.

The above experiments show the  role of nitrogen and phosphorus in the eutrophication process in
the water  of Lake Hakojarvi. In  order to get some information about eutrophicative effects of
domestic sewage and pulp  mill effluents, which are typical pollutants in  Finland, some data is
presented in the following from Lake Saimaa (Fig. 1) and two coastal areas in the Gulf of Finland.

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 54
Lake Water

In Lake  Saimaa,  which is  one of the largest lakes in Finland, phytoplankton production was
studied  in two areas  during  1968. The first area in northern parts of Lake Saimaa was being
polluted by about 12,000 m3/day of biologically purified domestic sewage. The second area was in
the south, and was polluted  by 260,000 m3/day of mechanically purified pulp mill waste. The
effluent consists of 44% sulphite  and 56% sulphate liquor (Lehmusluoto and Heinonen, 1970).
Preliminary tests were made by using algal assay bottle tests mentioned earlier.

Domestic sewage  biostimulated the algae growth in every concentration, but pulp mill effluents
were  almost  lethal to  algae at  10% effluent  concentrations. In  1%  and  0.1%  effluent
concentrations, algae growth was slightly stimulated {Fig. 4).

Primary production measurements from the lake water were made six times during the growing
season in constant light (5,000 lux) to eliminate the diurnal changes in illumination.

Domestic sewage caused increased primary production in the recipient. Phytoplankton production,
without any  depression near the  sewage outfall, decreased, as did the oxygen consumption in


                    ALGAL ASSAY
                    CELLS/LITER
                                           -	. DOMESTIC SEWAGE
                                                  PULP MILL EFFLUENTS
                                                     (SA + SI)
                     I06-
                            100  50   25    10    I    0.1   0
                        WASTE WATER CONCENTRATION IN LAKE WATER  %

 FIGURE 4   The influence of domestic  sewage and pulp mill effluents (sulphate, sa and sulphite,
             si liquor) in lake water (Lake Saimaa) as measured by algal assay in bottles. Test alga
             was Ankistrodesmus sp.
hypolimnion with distance. In  the hypolimnion there was no oxygen deficit in any region. The
greatest values of phytoplankton production (294.1  and 299.5 mg C/m3/day) were observed near
the outfall. At a distance of about 24 km from the  outfall, the primary production was 48.1 mg
C/m3/day (Table 3). This value can be used as an index for unpolluted water in that region.

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                                                                                      55
                                        TABLE  3

      Phytoplankton Primary Production mg C/m3/day in Northern Parts of Lake Saimaa
               as Mean Values of Six Measurements During the Growing Season

                      The Recipient is Influenced by Domestic Sewage

Distance from
Outfall, km                    248             12            24
mgC/m3/day                 294.1         299.5        239.7          170.4          48.1

The pulp mill effluents seemed at first to hinder phytoplankton primary production, but caused a
pronounced eutrophication  (752.9 mg C/m3/day) about 9 km from the outfall. At a distance of
about 22 km,  phytoplankton production was 175.2 mg C/m3/day (Table 4), and the water was
still slightly eutrophic.

It is shown that both domestic sewage  and pulp  mill effluents did  cause eutrophication of the
recipient.  Sewage  did  not have an inhibitive effect  as did  the effluents.  The  maximum
eutrophication caused by  the  pulp mill effluents  was more  intensive than that caused by the
domestic sewage, but it occurred far from the discharge area.

                                        TABLE  4

      Phytoplankton Primary Production mg C/m3/day in Southern Parts of Lake Saimaa
               as Mean Values of Six Measurements During the Growing Season

                      The Recipient is Influenced by Domestic Sewage

Distance from
Outfall, km                  -4           2          4           9          13        22

mgC/m3/day               93.1        177.9       285.6      752.9       548.8      175.2


Coastal Water

Eutrophication is not only a problem of  lakes but also of some coastal areas. Coastal waters in
Finland are brackish waters, partly meso- and oligohatine. Problems are concentrated usually near
the cities on the coast.

Helsinki, the capital of Finland, initiated in 1965 a research  program on the pollution of the Baltic
around the city. This was initiated because the archipelago near the city is an important recreation
area for  the citizens during the summer  time  and  the quality of the water was decreasing with
increasing eutrophication. This was mainly due to blue-green algae blooms in the later summer.


The City of  Helsinki was discharging its mechanically and biologically purified waste waters into
the nearby bays. These purification procedures seemed inadequate to control the eutrophication in
this coastal area.

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 56
 One part of the research program consisted of phytoplankton primary production studies. In this
 paper the results of one of the fjord systems of the year 1967 will be briefly dealt with.

 Phytoplankton production, mg C/m3 (max.)/day,  in the middle of the growing season at 1 km
 from the outfall  was about 30 times higher than that at 12 km distance in the unpolluted area
 outside Helsinki (Fig. 5). On the average during the growing season it was about 20 times higher
 (Table 5). Fluctuations  in primary production per square meter became irregular with increasing
 eutrophication (Fig. 6). Annual primary production in the innermost bay was 174 g C/m2/year,
 i.e. over 5 times higher than in the unpolluted  areas in  the Gulf of Finland where it was 30 g
 C/m2/year (Table 5).

                                        TABLE  5

      Primary Production g C/m2 /Growing Season and mg C/m3 (max.)/day on the Average
 in the Growing Season in a Fjord System in the Gulf of Finland off the Coast of Helsinki in 1967

 Distance from
 Outfall, km                   1           3           45          8         12

 g C/m2 /growing season      174         132         96          51         48        30

 mg C/m3 (max.)/day*      1092.6       950.8       533.9       133.9       99.6       58.9
 *Average for the growing season (eleven measurements).


 According to Jonasson (1969), in eutrophic waters  phytoplankton primary production acts in the
 following way.

         Primary production (per cubic meter) increases very sharply

         Fluctuations in primary production (per square meter) becomes irregular and

         Annual primary production (per square meter) may increase sharply.

 In coastal areas pulp  mill effluents  have a  quite similar influence as in the lakes. Two series of
experiments of phytoplankton  production in constant light, made in 1967 near the City of Kotka
in the Gulf of Finland, show this (Table 6). The phytoplankton primary production did increase to
a distance of 10-15 km from the outfall. In June, phytoplankton primary production did increase
to a  distance of 10-15 km from the outfall. In June phytoplankton production was low and it did
not increase at 20 km distance from the outfall. In  August eutrophication was obvious and  it
reached beyond 20 km from the outfall.
                                     CONCLUSIONS

Eutrophication of waters is a natural process, but as seen above, it can be greatly accelerated by
man. Therefore, it has become a recent problem in water protection. The increases in population,
industry and agricultural activities, for example, introduce excess nutrients and other  pollutants
into the waters. Nutrients may accelerate the development of eutrophication.

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                                                                                     57
                                       TABLE  6

           Primary Production near the City of Kotka in the Gulf of Finland in 1967

                              Data from Lehmusluoto (1967)
Distance from
Outfall, km

June, mg C/m3/day

August, mg C/m3/day
2
14.1
15.8
6
56.7
63.6
10
78.5
115.9
15
59.8
219.3
20
39.7
175.9
                             6 C/M'/DAY
FIGURE 5  Phytoplankton primary production off the coast of Helsinki in the Gulf of Finland at
            different stations on July 18,1967. The daily phytoplankton production is given in g
            C/m2/day.
                                         DISTANCE FROM OUTFALL  KM
               3-
               2.
                     FMAMJ'J'A'SWN i I i i i i ' i i  TTTT

                      MONTH

                       I 174 |      I IK I

                      6 C/MVYEAR
Hoi
FIGURE 6  Phytoplankton primary production g C/m2/day (solid line) at different stations off
            the coast of Helsinki in the Gulf of Finland in 1967. Total solar radiation (60° N) =
            kcal/m2/min (clashed line) (Smayda, 1959). The annual phytoplankton production is
            given in g C/m2.

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 58
Phytoplankton  primary production - as used  as  a measure  of eutrophication - reflects  the
ecological factors and algal succession. The most important factors are illumination, temperature
and nutrient  concentration of the water. The  annual  phytoplankton production (intensity of
eutrophication) is almost wholly dependent  on the nutrient concentration, and on the availability
of these nutrients. The influence of the other factors, despite annual fluctuations, may be almost
constant.

Domestic  sewage  and  pulp  mill  effluents are  important nutrient  sources  causing intense
eutrophication. Sewage is, thus, not the only type of waste water to cause eutrophication. Pulp
mill effluents  may also play a great part in the process, although their first influence seems to be to
hinder phytoplankton production. At some distance from the outfall, when the effluents have
been diluted,  phytoplankton production can proceed and the water eutrophicate.

The most important nutrients are nitrogen and phosphorus. Other substances, such as vitamines
and trace elements, must also be available. Many other growth stimulators are found in sewage.

It is important to consider all the  possible efforts to reduce nutrient input to receiving  waters in
any form in order to avoid overeutrophication of waters.
                                      REFERENCES
Bringmann,  G.  and Kuhn, R. (1956) Der Algen-Titer als Massstab der Eutrophierung von Wasser
     and Schlamm. Ges.-lng., 77, 374-381.

Demmerle, S. (1967) Der Einfluss von Humusstoffen auf das Algenwachstum, Manuscript.

Findenegg, I. (1964) BestimmungdesTrophiegradesvon Seen nach der Radiocarbon methode. Die
     Naturwissenschaften, 15, 368-369.

Fonden, R. (1969)  Heterotrophic bacteria  in Lake Malaren  and Lake Hjalmaren,  Oikos, 20,
     344-372.

Goldmann. C. R. (1962) A method of studying nutrient limiting factors in situ in water columns
     isolated by polyethylene film, Limnol. Oceanogr., 7, 99-101.

Gran, H. H. (1929) Investigation  of  the  production  of  plankton  outside  the  Romsdalsfjord
     1926-27, Rapp. Cons. Explor. Mer., 56, 1-112.

Hobbie, J. E. (1964) Carbon 14 measurements of primary production in two arctic Alaskan takes,
     Verb. Internal. Verein. Limnol., 15,360-364.

Hubel, H. (1968) Die Bestimmung der Primarproduktion des Phytoplankton der Nord-Rugenschen
     Boddengewasser unter Verwendung der  Radiokohelnstoffmethode, Internal.  Rev. ges.
     HydrobJol., 53. 601-633.

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                                                                                      59
Jonasson,  P.  M.  (1969)  Bottom  fauna  and  eutrophication.  In  Eutrophication:  causes,
    consequences, correctives, (ed. by  National  Academy  of Sciences,  Washington, D.  C.)
    274-305.

Jarnefelt, H. (1956) Zooplankton and Humuswasser, Ann. Acad. Sci. Fenn., A 31, 1-14.

Laaksonen,  R.  (1970)  Vesistojen  veden laatu, Vesiensuojelun valvontaviranomaisen vuosina
    1962-1968 suorittamaan tarkkailuun perustuva tutkimus, Maa ja vesiteknillisia tutkimuksia,
    17, 1-132, (English abstract).

Lehmusluoto, P. O. (1967) Selvitys kasviplanktonin perustuotannosta Kotkan edustan merialueella
    vuonna 1967,  Kymijoen vesiensuojeluyhdistys, 11, 1-7, (in Finnish).

Lehmusluoto,  P.  O.  (1968)  Kasviplanktonin  perustuotanto  Helsingin edustan  merialueella,
    Limnolgisymposion, 1967, 31-42, (English summary).

Lehmusluoto, P. 0.  (1969) Veden pieneliotoiminnoista ja niiden  mittaamisesta radioaktiivisen
    hiilen avulla, Vesianalyyttisia menetelmia, Suomalaisten Kemistien Seura, 57-64, (in Finnish).

Lehmusluoto,  P.   O. and   Heinonen,  P.  0.  (1970)  Eraiden  jatevesien vaikutus  Saimaan
    perustuotantoon, Vesi,4, 1-8, (in Finnish).

Leppanen,  T.  (1970)  Tutkimuksia  bakteerien  gtukoosin  kaytosta  Hakojarvessa  ja  siihen
    sijoitetuissa koealtaissa, Limnologian pro-gradu-tutkielma, 1-103, (in Finnish).

McCoy,  E. I. and Sarles, W. B. (1969) Bacteria in lakes:  populations and functional relations. In
    Eutrophication:  causes, consequences, correctives,  (ed. by National Academy  of Sciences,
    Washington, D. C.),  331-339.

Ohle, W. (1940) Chemische  Eigenart der smalandischen Seen, Verb. Internat. Verein. Limnol.,9,
    145-159.

Ohle, W. (1956)  Bioactivity, production, and energy utilization of lakes, Limnol. Oceanogr., 1,
    139-149.

Pechlaner, R. (1964) Plankton production in natural lakes and hydroelectric water-basis in  the
    alpine region of the  Austrian Alps, Verh. Internat. Verein. Limnol., 15,375-383.

Rodhe, W. (1958) Primarproduktion und Seetypen, Verh. Internat. Verein. Limnol., 13, 121-141.

Rodhe,  W.  (1969)   Crystallization  of  eutrophication  concepts  in  Northern   Europe,   In
    Eutrophication:  causes, consequences, correctives,(ed. by  National  Academy of QSciences,
    Washington, D. C.),  50-64.

Rodhe. W..  Hobbie,  J.  E.  and Wright, R. T. (1966) Phototrophy  and heterotrophy in high
    mountain lakes, Verh. Internat. Verein. Limnol., 16, 302-313.

Ryhanen,  R. (1968)  Die  Bedeutung  der  Humussubstanzen im  stoffhaushalt der Gewasser
    Finnlands, Mitt. Internat. Verein. Limnol., 14, 168-178.

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 60
 Sederholm, H. (1963) Veden humus mikrobien ravintona, Limnologian pro-gradu-tutkielma, 1-65,
     (in Finnish).

 Siapiro, J. (1957) Chemical and biological studies on yellow organic acids of lake waters, Limnol.
     Oceanogr.,2, 161-179.

 Skulberg, O. (1964) Algal problems related to the eutrophication of European water supplies, and
     a bio-assay method to assess fertilizing influences of pollution on inland waters. In Algae and
     Man (ed. by D. Jackson, New York), 262-299.

Smayda,  T. J.  (1959) The  seasonal  incoming radiation in  Norwegian and Arctic waters, and
     indirect methods of measurement, J. Cons. Internal.  Explor. Mer., 24, 215-220.

Steemann Nielsen, E.  (1952) The  use  of  radioactive carbon  (C14)  for measuring organic
     production in the sea, J. Cons. Internal. Explor. Mer., 18, 117-140.

Thomas, A. E. (1968) Die Phosphattrophierung des Zurichsee und anderer Schweizer Seen., Mitt.
     Internal. Verein. Limnol., 14, 231-242.

Wright. R. T.  and Hobbie,  J. E. (1965)  The uptake of organic  solutes in  lake water, Limnol.
     Oceanogr., 10,22-28.

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        THE  RECOVERY PROCESS OF A  LAKE WHICH RECEIVED
             WASTEWATER  FROM AN  ORE DRESSING PLANT
                                     Bengt Ahling
A question, on which interest is currently focusing in the problem-complex of industrial pollution,
is what happens to a recipient of industrial waste water if the industry closes down or improves its
waste water plant so that the addition of polluted water appreciably diminishes.

The question is  of very  great  importance from the standpoint to be  adopted in reference to
measures for the restoration of  polluted lakes. In those cases in which a recipient cannot, within a
reasonable time, purify itself to  the point to which its water can be used for the different purposes
that may be considered desirable, it may be necessary to take steps to restore the lake.
                                                Control lake
                               FIGURE 1   LakeBilsjan
                                         6

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 62
One of  the lakes that  has been investigated in order to study the recovery process is Lake Bal
(Balsjon) in Central Sweden. The area of Balsjon is 0.30 km2, and the mean and maximum depths
are 5 and 11  meters respectively. The catchment area is rather small, only 5.5 km2, and consists
mostly of marshes. Up to the  autumn of 1967 Lake Bal was receiving the waste water from a
dressing  plant  for magnetite  and  hematite.  The  dressing plant  operated  with  gravity and
wet-magnetic concentration  and therefore had  to use large  quantities of water. As the smallest
particles were very hard to  separate off  with  the methods  used, they followed with the  water
through the dressing plant.

The waste water was pumped to a banked-in area for sedimentation (Fig. 1).  From here the still
turbid water was conducted  via a settling dam to Balsjon. This made the water in Balsjon so turbid
that the Secchi disk transparency was reduced  to only a few centimeters. Owing to this turbidity,
light could not penetrate to  any appreciable depth, but was  reflected or absorbed in the topmost
layer of water.  In  Balsjon there was constant sedimentation of the fine-grained particles. This
meant that any organic substance eventually formed in  or  added to the  lake was  immediately
embedded in the sediment, which made Balsjon  a very sterile milieu for many organisms.

Before the plant closed down, Balsjon and a similar  lake used as a control  lake were investigated
for a couple  of years, so that  there was comparative material when it came to a  study of the
recovery of the lake. In order to be able to give a clear picture of the recovery it may be as well to
give an account of the situation  prevailing  before the plant closed down.

     QUALITY OF THE WATER WHEN THE  DRESSING PLANT  WAS  OPERATING

Chemico-physical Conditions

Turbidity, Color and Secchi Disk Transparency

The most striking effect of the  discharge  from the dressing plant was the marked turbidity of the
recipient. The heamtite sludge that was not utilized  imparted a distinct reddish color to Balsjon.
Through the  discharge this coloring was much intensified. The control  lake had a color value of
about 30 mg Pt/l, while values as high as 650 mg Pt/l were measured in Balsjon.

Owing to the turbidity, the Secchi disk transparency was reduced to only a few centimeters.

pHand Conductivity

The waste water had a pH  between 8.2  and 8.3 in the sedimentation basins. In Balsjon,  after
dilution, pH was between 7.8 and 8.1 in the spring and summer samples respectively. Owing to the
abundance of  unbound ions  in   the waste water,  the specific conductivity was  considerably
increased. The value in  Balsjon was about seven  times that in the control lake.

Iron Content

Due to the waste sludge, the iron content of the water was for the most part very high, as the iron
content of the particles was  about 15%. The highest content measured in Balsjon was 10 mg Fe/l,
which coincided with  a markedly reddish coloring  and turbidity. Analysis of the filtered and
unfiltered samples showed  that  most  of  the iron occurred  as  suspended material. A  not

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                                                                                        63
inconsiderable part {25%), however, occurred in such a form that it passed a fine filter paper.

Content of Oxygen

The oxygen content was  always  high  in Balsjon, showing values of about  90%  saturation. The
waste from the dressing plant thus did not affect the oxygen content negatively.

Consumption of Permanganate

The consumption of potassium permanganate in the water was determined. The result showed that
very small amounts of organic chemically oxidizable substance existed  in the water. The values
measured were about half of those for the control lake, or 10 mg KMn04/l.

Biological Conditions

The Balsjon water had a consistency of extremely fine-grained red sediment. This is unsuitable as a
substrate for more or less sessile living lake bed organisms. Balsjon was therefore characterized  by
the absence of such species as well as the greater part of the submerged plants. In the samples
taken from the lake bed, only a few odd specimens were found of Chaoborus, which swims freely
in the water near the bed, and of crustaceans of copepod type. In  the northern  part of the lake
there  were indications of  organic flocculi, and  in  connection  with these  a few protozoons,
Flagellata, and diatoms like Synedra.

Owing to the marked turbidity in Balsjon, the light could not penetrate to any appreciable depth,
so that autotrophic organisms were able to exist only in a very thin surface layer. This implied a
marked diminution of the lake's total production.
                Turbidity
               ZP-units
19000
1100-
1000-
500-
400-
300-
200-
100
en
D












D White - Balsjbn
Black — Control lake
















fll




—


1




-,


,
                         1967
                                    68
                    69
                                                                         year
                       FIGURE 2   Lake Balsjon:  Turbidity vs. Time

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 64
This meager production was especially noticeable in the result of the zooplankton counts, where
no  individuals at all  were found. There were, on the other hand, small specimens of pike (Esox
bicius), roach (Rutilus rutilus), perch  (Perca fluviatilis)  and  freshwater crayfish (Potamobius
astacus).

   THE  RECOVERY  PROCESS IN BALSJON  AFTER THE  CLOSING  DOWN OF THE
                         DRESSING PLANT IN  NOVEMBER 1967

Changes In The Physic-chemical Factors

Turbidity, Color, Iron Content and SecchiDisk Transparency

When the discharge of waste water stopped, the particles existing in the water settled. This resulted
in reduced turbidity  (Fig. 2} and increased Secchi disk  transparency (Fig. 3). The lake, which
earlier had had a marked red coloring, began to assume a considerably more normal hue. This is
also seen in the color measurements in Fig. 4, which show that the color values in Balsjon were
beginning more and more to agree with those in the control lake.

In connection with sedimentation of suspended particles, the iron content was of course reduced
to a range of values corresponding with that in the control lake (Fig. 5).

The variations now  occurring in turbidity and  in  the Secchi disk transparency  are due to the
addition of particles  from the surrounding embankment of waste. After a spring flood or heavy
rainfall, this addition  is  noticed as a transient red coloring  of Balsjon.
           Secchi  disk transparency
                m
              3-
White  — Balsjon  -
Black  — Control  lake
                                                 I
                                                 1
                     1967         68         69         70          71

                FIGURE 3  Lake Balsjon:  Secchi disk transparency vs. Time
                    year

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                                                                                          65
                 Color    4OO
                mg pt /1
               250


               200-


               150-


               100-


                50-

                25-
                                                         White  - Balsjon
                                                         Black - Control lake
•
                                                  n
                      1967       68        69        70        71

                        FIGURE 4   Lake Balsjon: Color vs. Time
                    Total iron
                     mg Fe/ I  9 70
                                year
25-
2.0-
1.5-
1.0-
0.5-




u
1






i
"
,






White - Balsjdn
Black - Control It



I 1 Ifin
                         1967       68       69       70       71     year

                      FIGURE 5   Lake Balsjon:  Iron content vs. Time
pHand Conductivity
A certain reduction of pH was observable in the spring samples, while the autumn samples even
showed an increase. This may be interpreted to mean that the concentration of the pH-increasing
substances had been reduced, which led in turn to a reduction of pH. Furthermore, the primary
production increased, which gave increased pH during the production period.

The big difference earlier noted between the specific conductivity of Bilsjon and the control lake
respectively began gradually to lessen. (Fig. 6). The slowness of this lessening was due to the very
slight water turnover in the lake.

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 66
                   Electrical  conductivity
Of 2
300-

200-

100-

0-10"
White - Batsjbn







1







1
Black - Control lake



1

n
n
i in


i



                          1967
                                           69
                                                    70
                                                                  year
                FIGURE 6  Lake Balsjon:  Electrical conductivity vs. Time
Oxygen Content and Consumption of Permanganate

After the closing down of the dressing plant the values for the oxygen content were still high. In
some samples of water from the bottom of the lake, however, an oxygen deficit down to 17%
saturation was observable. This indicates that organic substance may have been added or formed in
the lake in such quantities as to have had an effect on the oxygen economy of the lake.

The consumption of permanganate had  increased to such an extent in Balsjon that it coincided
with that in the control lake, (Fig.  7) which implied that the quantity of organic substances in the
Consumption of
Permanganate
mg KMnO^ White — Balsjbn
70-
60-
50 •
40
30 •
20 -
10




1 n
11 II
Black — Control lake



''1
II. 1
                         1967       68        69        70        71      year

                FIGURE 7   Lake Balsjon:  Permanganate consumption vs. Time

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                                                                                        67
water had increased. This increase was an indication that the primary production in the lake had
increased, or that permanganate-consuming substance had been added to the lake.

Nitrogen and Phosphorus

Nitrogen and  phosphorus show higher values as in the control lake. There has not yet, however,
been any change in the values.

Changes In The Biological Conditions

Phytoplankton

After the disappearance of turbidity the occurrence of phytoplankton markedly increased (Fig. 8).
This applied especially to the diatoms, where during the  autumn and winter Cyclotella comensis
and to a certain extent also Synedra acus showed high values for the number of  individuals (on 4
November  1969, for instance, there were 3 million Cyclotella per liter). In the spring and summer
the Chrysomonad Rhodomonas lacustris and the earlier  completely absent Dinobryon divergens
occurred in considerable quantities.

Apart from this increased number of individuals, the number of species,  especially of Chlorophyta,
increased (Fig. 9). Newly added species were e.g. Elakatothrix gelatinosa and Gloeocystis. The new
species in Balsjon were still of very slight  importance for the total production of the  lake. From
the general  picture of plankton it emerged  that there was a relatively large' number of individuals
belonging to  a  small number  of  species (Fig. 10); this  gave the picture of an extreme milieu.
However, the  increasing number was an indication that the milieu was becoming less extreme.

If we compare the composition of species in Balsjon with that in the control lake (Fig. 11) we find
a considerably greater variety in the latter, with a larger number of species represented.
                3-1
                  !05-
                      Total numbers
                      of individual
                      phytoptankton
                                                           White — Balsjon
                                                           Black - Control lake
                         67
                                  68
                                            59
70
                                                              71
                                                                    year
                      FIGURES   Lake Balsjon:  Phytoplankton vs. Time

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  68
                   30-
                   20-
                   10-
                     Number of species of
                     phytoplankton
I
                                             I
                                                          White — Balsjcn
                                                          Black -Control lake
                        1967
                                 68
                                          69
                                                   70
                                                                 year
                  FIGURE 9  Lake Balsjon:  Phytoptankton species vs. Time
Zooplankton

Two years after the closing down of the dressing plant Balsjon showed a zooplankton composition
almost identical with that in the control lake. The differences referred exclusively to the number
of individuals. Thus the number of Ciliata in the control lake was about 10 times greater than in
Balsjon,  and other zooplankton were 5 times more numerous. Although  Balsjon still showed a
paucity in the number of individuals as compared with the control lake, the zooplankton existing
there implied a marked increase compared with the earlier total absence of these organisms.

Among  the  zooplankton  occurring,  the  predominant  species  were the  rotifers Polyarthra,
Gastropus stylifer and Keratella cochlearis. Other zooplankton species of Cladocora and copepoda
occurred in Balsjon only as isolated individuals.

Lake Bed Fauna

When the rain of particles over the sediment surface stopped, the fauna normally living on the lake
bed could once more start colonizing it. During the investigations carried  out the year after the
closing down of the dressing plant, it was possible to observe only very slight changes. One only
found scattered specimens of Ephemeridae and Chironomidae in the lake bed samples taken.

It was not until  one year later, during the summer  and autumn of 1969, that it was possible to
observe that a  community of organisms was in the process of being built up. Ephemeridae, in
1970, were of general occurrence. It was, however, only Ephemera vulgata that occurred, and this
gave an impression of the instability of the system.

The groups of lake bed organisms most common in Balsjon two years after the closing down of the
dressing  plant  were  Chironomidae and Ceratopogonidae. Of the Chironomidae,  Chironomus
plumosus were  abundantly represented, but  large  numbers of  organisms from  the subfamily

-------
                                             Balsjbn
100-
90-

80-
:

:
- -
40-
:..

;; .
.


























'A
V,
Y;






X







— 1 fr
y
/

y
y



I


_
y


^

^
y
y

^
,








'
• -
                     1967
                                :
                                           -

                                                                                        69
                                                             • Cyanophyta
                                                             ^ Chlorophyta
                                                             H Chrysomonadinae
                                                             ^ Diatomeae
                                                             C Pyrrophyta
                                                                71
                                                                       year
                     FIGURE 10  Lake Balsjon:  Percent of species vs. Time
                    .
•  Cycnophytc
E  Chlorophyta
H  Chrysomonadinae
0  Diatomeae
LH  Pyrrophyta
                                                                Control  lake
100-
90-
:
-
:

40
30
.


7
^
2.


\
                       1967        68        69        70               year
                    FIGURE 11 Control  Lake: Percent of species vs. Time

Tanypodinae also occurred. Of the Ceratopogonidae, Palpomyia was the animal occurring most
generally in the whole system even if a smaller number of Chaoborus also occurred. It was possibl
to find a greater density of organisms if one went to the northern part of the lake. This was the
part furthest from the region where the waste was introduced into Balsjon, so it thus got the I
sedimentation  of  particles over the sediment surface. It was also possible to find a considerably
more modified community of organisms in the discharge canal  in the south end of the lake
the water had  little depth and the surrounding reeds contributed organic material which promoted

-------
 70
the colonization  of the  lake bed organisms. Apart from the already mentioned organisms one
found in this canal Herpobdella, Asellus and large quantities of mites.

Owing to the  small amount of organic material on the bottom, the lake bed organisms had very
poor  protection against predacity. This predacity must have certainly been a strongly reducing
factor as regards these organisms. Analysis of the gastric contents of fish from Balsjon also showed
the organisms mentioned in the foregoing.

Other Changes

Apart from the changes  mentioned  in the community of organisms, it was possible to make a
number of studies through visual examination of the lake. These changes were very difficult to
assess quantitatively, and the observations thus made were, accordingly, very subjective.

On the  lake shores one could  see  great swarms of the ostracod  Notodromas monacha. This
organism commonly occurs in stagnant little lakes during the summer. It is, however, extremely
unusual  to find such mass development as was here.

At the edge of the shore at the populations of Phragmites that existed, it was possible to observe
large shoals of one-year-old perch and a  large number of pike. Such shoals often occurred near
shoals of Notodromas, which indicates that the ostracod may be an object of nourishment for the
small fry among the fish.


The first traces of Periphyton began to appear on the lake  bed. These were the thread-formed algae
Zygnema and Spirogyra which had begun to spread to the regions where the light was earlier too
weak  for these autotrophic algae.

In the cores of sediment collected  in Balsjon in 1969 it was possible to find traces of organic
material. This  was composed of detritus and vegetable  fiber that was presumably  only partly
produced in the lake and had otherwise  come from  the soil surrounding the lake.  Besides this
material there were also shells and remains of diatoms and  Crustacea.

This study of  lake recovery reached  one of the most interesting stages in 1970. The first part of
the recovery referred chiefly to the physio-chemical  factors and was a relatively simple process
which was mainly  a question of sedimentation rates. The most important question for this process
in the near future  is how  rapidly the embankments of waste along the shores can be bound by
vegetation. This is important for the prevention of  inorganic material being washed out into the
lake by rain and melt water.

The second stage, which referred chiefly to the building up of a balanced biosystem, is a good deal
more  difficult to foretell. The results hitherto obtained  show that the number of species in the
system  is on  the  increase. They also show that certain species very  easily  begin  to become
predominant with a mass development. This is presumably a tendency that will continue until an
organic  layer has been formed above the inorganic sediment. This organic layer is essential to give
the different  organisms protection  against  predacity.  When they have this protection the
fluctuations due to this predacity will be reduced.

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              DEPLETION  OF  OXYGEN  BY MICROORGANISMS
              IN  ALASKAN  RIVERS AT LOW  TEMPERATURES
                                   Ronald C. Gordon
                                   INTRODUCTION

Several arctic (Lotspeich, unpubl; Schallock, unpubl) and subarctic (Prey, 1969; Gordon, unpubl;
Mueller,  unpubl; Schallock, unpubl) rivers in Alaska (Alaskan rivers) have low concentrations of
dissolved oxygen (DO) during periods of total ice cover; conditions which occur naturally without
domestic or industrial pollution. A similar oxygen deficit was noted in some unpolluted rivers in
the northern and central belt of the U.S.S.R. (Drachev, 1964). Data from various subarctic rivers
in Alaska indicated that DO depletion was a continuous process throughout most of the period of
ice cover,  with an  increase  in  DO concentration shortly before spring  breakup  (Frey, 1969;
Gordon,  unpubl; Schallock, unpubl). The extent of depletion increased progressively toward the
lower reaches of each river (Frey, unpubl; Gordon, unpubl).

Investigations in the U.S.S.R. have shown that the low DO concentration resulted from the ice
cover which prevented reaeration (Drachev,  1964). Since there is essentially no open water during
the period of ice cover over many Alaskan rivers, there is little chance for significant reaeration.
Under natural conditions, the extent of oxygen depletion is often sufficient to reduce the DO
concentration to a level far below the 7  mg/l minimum set by the Alaska water quality standards
(State of  Alaska,  1967).  A DO concentration  of  1.1 mg/l was measured  in an unpolluted arctic
river  {Lotspeich,  unpubl; Schallock,  unpubl)  and, 1.1  mg/l (Gordon,  unpubl)  and   1.0 mg/l
(Roguski, 1967) in unpolluted subarctic rivers.

The aquatic biota of Alaskan rivers seem to survive the extreme fluctuations in the amount of DO
which they encounter throughout the  year  under  natural conditions.  Problems arise when
oxidizable domestic or industrial wastes enter these rivers. When the biochemical oxygen demand
(BOD) of these wastes is added to the natural requirement for DO, the result may be detrimental
to the ecosystem.

Ingraham and Stokes (1959)  discussed the numerous definitions of psychrophilic bacteria and set
forth what is probably the most useful definition, "Psychrophiles are bacteria that grow well at 0°
C within 2 weeks". These organisms appear  to be ubiquitous in nature since they have been found
in soil, rivers, lakes, mud and food (Farrel and Rose, 1967; Stefaniak, 1968, Stokes and Redmond,
1966). Psychrophiles have been studied in both the Arctic and Antarctic and  have been found in
soil  and  water  (Boyd, 1958;  Boyd and  Boyd, 1967; Fournelle,   1967; McDonald, et al., 1963;
Straka and Stokes, 1960). These organisms  and their activity at low temperatures  have  been the
subject of several reviews (Farrell and  Rose, 1965; 1967; Ingraham and Maaloe, 1967;  Ingraham
and Stokes, 1959; Miller,  1967) and will not  be  discussed  in detail here. Stokes and Redmond
(1966) considered psychrophiles to be present  in large  enough numbers in natural  habitats to be
important in the cycling of matter. Wuhrmann, et al. (1966) stated, "Self-purification  processes
start  at  the microbial level.  .  ."  and,  "Most of the work is accomplished  by  heterotrophic
microorganisms (bacteria, fungi, flagellates)".
                                          71

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 72


Active metabolism of organic material  in a river during the winter has been demonstrated in the
U.S.S.R. (Drachev, 1964). Plate counts of heterotrophic bacteria indicated that Alaskan rivers have
bacterial populations  in the range of 104 - 106 organisms/ml which are capable of growth  on a
synthetic medium at  low temperatures(Gordon,  unpubl).  There is evidence that the number of
organisms capable of growth at low temperatures increases progressively toward the lower reaches
of a subarctic river in Alaska  (Gordon, unpubl) and  in a river in the U.S.S.R. (Drachev, 1964)
during the period of total ice cover.

It has been shown that psychrophilic bacteria  are  capable  of rapid metabolic activity  at low
temperatures. Since Alaskan rivers have populations of these organisms, it appears that they may
be responsible  for a  significant portion of the DO depletion observed under  both natural and
polluted conditions.  The subject of  this report is  DO depletion by the indigenous bacteria in a
subarctic river.  The effect of added organic and inorganic nutrients and incubation temperature on
the rate and extent  of  DO depletion was investigated. The data obtained from a subarctic river
were compared  to similar data from an arctic river.

                              MATERIALS  AND METHODS

River Description And Sampling Locations

Most of the experimental results were obtained from a subarctic river in interior Alaska. Because
of the high level of domestic pollution in the lower reach and the convenient location, the Chena
River was chosen for detailed study. It is a nonglacial stream with many ground water sources, and
is approximately 150 miles in  length (Frey,  1969). Raw domestic sewage and effluents from
several primary sewage treatment plants in the greater Fairbanks area enter the river in the last 28
miles before it joins the Tanana  River. Two sampling locations were selected, one below all major
sources of domestic pollution and the other above any source.

Comparative data were  obtained  from an arctic river in the  "Arctic Slope" area of Alaska. The
Sagavanirktok  (Sag)  River was selected because  it is  the major river flowing through an area of
extensive oil development and  is accessible for sampling. It  is a nonglacial stream originating in the
Brooks Range, flowing north approximately 170 miles to the Beaufort Sea and receiving little, if
any, domestic pollution (Gordon, unpubl). One sampling location was selected approximately 85
river miles above the mouth of  the river near the settlement of  Sagwon.

Sample Collection And Handling

All sample locations had total ice cover and a water  temperature of essentially 0° C throughout the
study  period. Samples were obtained through holes drilled  in the ice. Samples  from the Chena
River  for  the  dissolved oxygen  (DO)  depletion  study  were collected in sterile five gallon
polypropylene  carboys  by dipping water  from the hole in the ice. Because of the large volume
required, no problem with increase of water temperature was encountered during the 2 to 3 hour
period between sample collection and handling in the laboratory.

Samples from the Sag River for  the DO  depletion study required somewhat different handling.
These  samples were collected in new, clean, but not sterile, five gallon polyethylene carboys which
were sealed with  tight screwcaps. It was not possible to dip the water, so it was pumped into the
carboys. The samples were shipped by air freight to the laboratory. The water temperature rose

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                                                                                        73
from approximately 0° to 3.5° C during the 9 hour period between sample collection and handling
in the laboratory. This temperature rise did not appear to be excessive, and was not considered
significant.

Samples for  chemical analysis were  collected in small mouth  250 ml  screwcap  polyethylene
bottles. These bottles were filled by submerging them in the hole drilled in the ice and returned to
the laboratory without further field treatment. They were frozen as soon as possible after arrival at
the laboratory and stored at -20° C until they were analyzed.

Samples for  the determination of DO in  the river were collected in 300 ml biochemical oxygen
demand  (BOD) bottles. The bottles were lowered on  a rod  sampler below the bottom of the ice,
allowed  to fill completely, and the  oxygen was fixed immediately  after being brought to the
surface.

Handling Of Samples In The Laboratory For DO Depletion Studies

After the samples  were returned to the laboratory,  they were taken directly into the 10° C  cold
room. The DO depletion study was set up immediately, using pre-cooled glassware to minimize
any adverse  effect on  the  natural  distribution  of  the microorganisms in  the  samples. A
predetermined volume of  river water, 24-36 liters, and the substrate being studied were placed in a
2'/2 or 3'/2 gallon,  sterile,  glass carboy. The carboy was placed on the apparatus shown in Figure
1-A. The water was stirred rapidly with a  magnetic stirrer while  the temperature  was raised 1°  -
FIGURE 1   Apparatus for preparation and bottling of river water samples for dissolved oxygen
            depletion studies. (A) Sample was stirred vigorously  while the temperature was
            equilibrated  at  1° - 1.5°  C above the  desired incubation temperature with  a
            thermostatically controlled, 1000 watt, Vicor glass, immersion heater; followed by
            dissolved  oxygen equilibration at or near saturation by aeration with a gas dispersion
            tube. (6)  Equilibrated sample was pumped into biochemical oxygen demand bottles
            for incubation.

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 74
 1.5° C above the intended incubation temperature with a thermostatically controlled, 1000 watt,
 Vicor glass, immersion  heater. The  increase in temperature above that selected for incubation
 prevented supersaturation of the water  with  DO. When the desired  temperature was reached,
 stirring was continued and the water was aerated vigorously for 10 minutes using a gas dispersion
 tube to bring the DO level to or near saturation. After temperature adjustment and aeration, the
 river water was pumped into BOD bottles as shown in Figure 1-B. The bottles were filled from the
 bottom to prevent  entrainment of  additional  DO.  The  initial DO  level was determined by
 immediately fixing the oxygen in three of the BOD bottles. The rest of the BOD bottles were
 placed in  incubators at  0°, 5°, 10°, 15° or 20° C. Time intervals were selected to permit the
 depletion of DO to be followed. The DO was determined in three bottles at each time interval.

 Substrates Used For DO Depletion Studies

 Several  laboratory substrates of varying complexity were  used. Vitamin-Free Casamino Acids,
 Control 534363 (Difco) were used to compare rates of DO depletion at several temperatures, with
 water from various sources, and as a control for other  studies. Yeast Extract, Control  523143
 (Difco)  and Beef Extract, Control 495576 (Difco) were  used as complex substrates containing
 growth factors. Growth factors are defined as organic compounds, generally in minute amounts,
 required for growth  by an organism  in addition to the principal sources of carbon and energy.
 Glucose (Dextrose, Control 527712, Difco) was used to represent the carbohydrates. Ethyl alcohol
 (dehydrated,  N.F.,  Federal Government stock  no. 6505-105-0000)  was the only alcohol used.
 Sodium acetate NaC2H3O2-3H2O,  Mallinckrodt  analytical  reagent)  was used to represent the
 organic acids.

Primary and secondary sewage treatment plant effluents were also studied. Primary effluent was
obtained from the Fairbanks city plant before the effluent entered the chlorine contact chamber.
Secondary effluent was obtained from a bench scale activated sludge system being operated in the
Alaska Water Laboratory at 0° - 1.0° C.

 Enumeration And Isolation Of Heterotrophic Bacteria

The membrane filter method and a  broth  culture medium prepared from components  [2.5 g/l
Yeast Extract  (Difco), 5 g/I Tryptone (Difco), and  1 g/l Dextrose (Difco) made up in glass distilled
 water and adjusted to pH 7.0 at 25° C before autoclaving] were used to enumerate bacteria at 0°
 C. This medium was found to give higher numbers on membrane filters at 0° C than any other
 medium tried  (Gordon,  unpubl). However,  this does not mean that these were the only bacteria
 present in the water. All membrane filter preparation was done  in  the 10° C cold  room, using
 pre-cooled equipment and materials. Incubation of filters was continued until there was no further
 increase in numbers on consecutive counts.

 Isolation of pure cultures was accomplished by  picking individual colonies from the membrane
filter after the  number of colonies had stopped increasing. The colonies were placed in tubes of the
 same broth medium used for initial  enumeration, and incubated at 5° C because growth was more
 rapid than at 0° C. After growth appeared, material from the broth cultures was streaked on Plate
 Count  Agar (Difco) and incubated at 5° C. Individual colonies were picked and grown in broth.
 This procedure was repeated as a final check of culture purity. The pure cultures were maintained
 for further study by monthly transfer to fresh broth and incubation at 5° C.

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                                                                                      75
Chemical Analyses

The Technicon Auto Analyzer was used for the following analyses:  Orthophosphate phosphorus
by trie Technicon ammonium molybdate industrial  method; ammonia nitrogen  by the  sodium
phenolate  method  (FWQA,  1969);  nitrite  nitrogen by  diazotization  (FWQA, 1969); nitrate
nitrogen by hydrazine reduction (FWQA, 1969).

Total  nitrogen and total carbon were  determined with the Perkin-Elmer model  240 Elemental
Analyzer.

Total phosphorus was determined by the persulfate digestion method (FWQA,  1969), except for
glucose. Glucose samples were ashed  (AOAC, 1965),  followed by the orthophosphate phosphorus
determination previously described.

Chemical oxygen demand was determined as described in the 12th edition of Standard Methods
for the Examination of Water and Wastewater (APHA, 1965).

DO was determined by the azide modification of the iodometric method (APHA, 1965).
Statistical Treatment Of DO Depletion Data

Each set of 3 DO measurements was evaluated by the Q Test to reject questionable results. The
remaining measurements were averaged to obtain the reported result. To compare rates of DO
depletion, an attempt was made to establish a rate constant with one substrate at each incubation
temperature. Data obtained during the period of most rapid DO depletion were treated with first
and second order kinetics, and did not fit either form. The arithmetic form, DO vs time, provided
the most useful treatment of the data. A straight edge was laid along the slope of the DO depletion
curve, and the data  points on the portion of the curve which appeared to have the most rapid rate
of change were used to establish an approximate rate (mg/l/hr) for the purpose  of comparing data
within this study.

                                       RESULTS

Pure Culture Study Of Psychrophilic Bacteria Isolated From A Subarctic River

Water samples were collected from a polluted and an unpolluted location in a subarctic (Chena)
river on December  17. 1968 and contained, respectively, 9000 and 550 heterotrophic bacteria per
ml which were capable of growth at 0° C on the complex organic medium as described in the
Materials and Methods section. AH colonies on a representative membrane filter from each location
were isolated  in pure  culture. Broth  tubes inoculated with  the pure cultures  were incubated  as
shown  in Table 1. All cultures from both locations grew at 0°, 5°, and 10°  C, but not at higher
temperatures. The  percentage of the total number which did grow at 20° C and 25°  C was the
same from both locations. At 30° C and above, the percentage of cultures from the polluted
location that  grew decreased  much more slowly  than those  from the unpolluted  location. This
suggested that domestic pollution caused a change  in population composition.

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76
Parrel I and Rose (1967) pointed out in their review that Gram negative rods are the most common
psychrophilic bacteria  isolated, both qualitatively and quantitatively. Gram  negative rods have
been isolated from littoral and marine sediments in the Canadian Arctic (McDonald, et al., 1963)
and were  the most common bacteria isolated from water in subarctic Alaska (Fournelle, 1967).
Farrell and Rose (1967) referred to phychrophilic members of the genus Vibrio (spiral bacteria) as
not being as common as the Gram negative rods, but still isolated regularly.

Further study of the pure cultures revealed that only Gram negative rod and spiral morphological
types of  bacteria  had  produced  colonies on the original  membrane filters.  The  effects of
incubation temperatures on the two types of bacteria from  each  location are shown in Table 2.
The data, from the unpolluted  location, indicated that  increasing the incubation temperature
above 25° C caused a more rapid decrease in  the percentage of the spiral than of the rod shaped
bacteria which  grew. The  results from the polluted location were similar except that the more
rapid decrease of spiral bacteria took place above 30° C rather than 25° C. An additional point of
interest was that all the spiral bacteria grew at 20° C, but some of the rods from both locations
were inhibited at this temperature.

Examination of Table 2 shows that the ratio  of rod to spiral bacteria  changed from 1.5:1 at the
unpolluted location to 2.9:1 at the polluted  location. This twofold  increase of rods relative to
spiral bacteria  was further  indication that domestic  pollution altered the composition of the
bacterial population.

                                        TABLE 1

         Effect of  Increased Incubation Temperature on the Growth of Bacterial Isolates
                      from Samples Obtained from a Subarctic River3'

Incubation
Temperature                             _        Sample Location                 H
                                Polluted?                             Unpolluted"
                      Number of         % of Total          Number of          % of Total
                      Isolates            Isolates             Isolates             Isolates

  0° -10°  C               66                 100                38                100
     20                  63                 95.5               35                 92.1
     25                  52                 78.8               30                 78.9
     30                  49                 74.2               11                 28.9
     35                  22                 33.3                 6                 15.8
     45                   7                 10.6                 1                  2.6

    Total                  66                                    38

     a.    Samples were taken on December 17, 1968, when the river  had total  ice cover and the
          water temperature was 0   C.

     b.    The isolates  were obtained by picking all colonies from a membrane filter which had
          been incubated  at 0° C  until there was  no further increase  in numbers on consecutive
          counts.

     c.    The polluted location was below a  reach of the river receiving raw domestic sewage and
          effluents from primary sewage treatment  plants.

     d.    The  unpolluted  location was  upstream from  any source  of domestic  or industrial
          pollution.

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                                                                                        77
                                        TABLE 2

                 Relative Distribution and the Effects of Increased Incubation
             Temperature on the Growth of Two Morphological Types of Bacteria
                             Isolated from a Subarctic River3'
 Incubation
 Temperature
   0-10 C
     20
     25
     30
     35
     45
Total
                                Rod
                          Morphological Type
                                                                     Spiral
                          Sample Location
                     Polluted^          Unpolluted?
                                              Sample Location
                                            Polluted
No. of
Isolates
49
46
46
35
19
7
%of
Isolates
100
93.9
93.9
71.4
38.8
14.3
No. of
Isolates
22
20
18
10
5
1
%of
Isolates
100
90.9
81.8
45.5
22.7
4.5
No. of
Isolates
17
17
16
14
3
0
%of
Isolates
100
100
94.1
82.4
17.6
0.0
No. of
Isolates
15
15
12
1
1
0
%of
Isolates
100
100
80.0
6.7
6.7
0.0
49
22
                                                        17
                                                          15
    a.   Samples were taken on December 17, 1968, when the river had total ice cover and the
         water temperature was 0  C.

    b.   The isolates  were obtained by picking all colonies from a membrane filter which had
         been incubated  at  0 C until there was no further increase  in numbers  on consecutive
         counts.
    °'    ^ P°lluted location was below a reach of the river receiving raw domestic sewage and
         effluents from primary sewage treatment plants.

    d.    The unpolluted location was upstream  from any source of domestic or industrial
         pollution.
Effect  Of Complex Organic  Substrate  Concentration And  Incubation  Temperature  On  The
Dissolved Oxygen (DO) Depletion In Subarctic River Water

Vitamin-free casamino acids had been used previously in  pure  culture studies of Pseudomonas
fluorescens at low incubation temperatures (Jezeski and Olsen, 1961; Olsen  and Jezeski, 1963) and
were found  to give excellent growth, which was not enhanced by the addition of yeast extract. In
view of these earlier reports, some preliminary results from  this laboratory and the relatively
simple composition of the substrate, vitamin-free casamino acids were selected as the baseline and
comparative substrate.

The effect of substrate concentration on DO depletion in polluted river water is shown in Figure 2.
These data indicated that a vitamin-free casamino acids concentration of 120 mg/l was sufficient
to eliminate the substrate as a rate  limiting factor in DO depletion. There was no lag phase at 20°
C and the DO concentration in the  water was reduced to nearly 0 mg/l in 15-16 hours. A similar
effect of substrate concentration was observed at 10° C, but the time required to deplete the DO
from near saturation to 0 mg/l was approximately 50 hours.

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 78
                                         68   10   12   W
                                          TME (HOURS)
FIGURE 2  Effect of the concentration  of a complex  organic substrate on dissolved oxygen
            depletion in sub-Arctic river water polluted with raw domestic sewage and effluents
            from  primary treatment plants. Samples were incubated  at 20° C. Symbols: •, 90
            mg/l; A, 120 mg/l; and A, 150 mg/l vitamin-free casamino acids; o, river water blank.
Since the  water  temperature  in the Chena  River rarely, if ever,  rises above 20° C (Frey, 1969;
Gordon, unpubl), temperatures between 0° and 20° C were selected for incubating samples. The
effect of  incubation temperature on DO depletion  in polluted Chena River water is shown in
Figure 3. The volume of water obtained from the river was large enough to supply samples for all
incubation temperatures. This provided directly comparable temperature effect data when  the
samples were incubated in the presence of 120 mg/l vitamin-free casamino  acids. The results
indicated that the length of the acceleration phase  increased and the rate of  DO depletion was
reduced as the incubation temperature was decreased, and there was a short lag phase at the 0° C
incubation temperature. However, the extent of DO depletion did not appear  to be temperature
dependent.

Comparative results on the effect of incubation temperature were obtained with unpolluted river
water (Fig. 4). The results showed that there was a lag phase at the lower incubation temperatures
(0°, 5°, and 10° C) before the acceleration phase began.  This was in contrast to the lack of a lag
phase with samples from the polluted location. The extent of  the DO depletion, as found with the
sample from  the polluted  location, did not  appear to be temperature dependent.  However, the
total elapsed time was increased 50-100  percent.

The Relative Effect Of Complex Organic Substrates On DO Depletion In Subarctic River Water

Most of the psychrophilic bacteria are found in a few genera  (Farrell and Rose, 1967) and some
have been isolated from water in subarctic Alaska  (Fournelle, 1967).  Nutritional  studies.have
shown that the growth requirements vary over a wide range, from the simple need for a carbon and
energy source to the need for vitamins and  other preformed  growth factors (Adams and Stokes,

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                                                                                      79
                 2 -
                                      SO  100  120
                                      TIME (HOURS)
                               200
FIGURE 3  Effect  of incubation  temperature on  dissolved  oxygen  depletion when 120 mg/l
           vitamin-free casamino acids were added to sub-Arctic river water polluted with raw
           domestic sewage and effluents from primary sewage treatment plants. A river water
           blank (A) was incubated at 20° C.


1968; Jezeski and Olsen, 1961; Mulder, 1964, Olsen and Jezeski, 1963; Pereira and Morgan, 1957;
Prince, et al., 1954). Vitamin-free casamino acids contain 18 amino acids and essentially no other
growth factors, while yeast and beef extracts contain many amino acids, vitamins and other water
soluble growth factors.  The use of these three substrates for DO depletion studies permitted  an
examination of the effect of added growth factors.
                               40
80   120   160  200  240  280
    TIME (HOURS)
FIGURE 4  Effect of incubation temperature on  dissolved oxygen depletion when 120  mg/l
           vitamin-free casamino acids were added to unpolluted sub-Arctic river water. A river
           water blank (A) was incubated at 20° C.

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80
All the bacteria isolated from both locations were  capable of growth at  10°  C on a complex
medium containing a variety of preformed growth factors (Table  1), and DO depletion with river
water samples took place in  a reasonable time at 10° C with  vitamin-free casamino acids as the
substrate (Figs. 3 and 4). Since 10° C appeared to be adequate for growth and metabolic activity,
it was selected as the incubation temperature for additional studies.

Water samples from both sample locations were incubated at 10° C with the three complex organic
substrates in quantities containing the  same amounts of carbon.  The  results are presented  in
Figures 5 and 6. The acceleration phase of the DO depletion curve was shorter with samples from
both  locations  when the  yeast or beef extract  was used as  the substrate. This suggested  that
preformed growth  factors either enhanced overall  metabolic activity  or were required by a portion
of the bacterial population. The results  indicated  that there was a difference in  the relative effect
of yeast and beef  extracts on  DO  depletion at each location. The  yeast extract  caused a very
pronounced decrease  in the acceleration phase as related to either  of  the other substrates when
incubated with water from the unpolluted  location (Fig. 6),  while the effect in water from the
polluted  location did not become apparent until later (Fig. 5). This could mean (a) that one  or
more  growth factors were added  with the sewage or (b)  that the bacteria enhanced by domestic
pollution  (Table  1)  did not require the growth  factors  in yeast extract and  that those which
required growth factors needed a much longer time to utilize significant DO.
                                           20   30  40
                                           TIME (HOURS)
                                                         50
FIGURE 5   Relative effect of three complex organic substrates on dissolved oxygen depletion in
             sub-Arctic river water polluted with raw domestic sewage and effluents from primary
             treatment plants. Samples were incubated at 10° C. Symbols: o, river water blank; A,
             120 mg/l vitamin-free casamino acids; •, 106 mg/l beef extract; O, 80 mg/l yeast
             extract. All three substrates contained equal amounts of carbon.

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                                                                                       81
                                         30  40  5O
                                         TIME (HOURS)

FIGURE 6  Relative effect of high levels (substrate not rate limiting) of three complex organic
           substrates on dissolved oxygen depletion  in unpolluted sub-Arctic river water when
           incubated at 10° C. Symbols: o, river water blank; •, 120 mg/l vitamin-free casamino
           acids;  A, 106  mg/l beef extract; A, 80  mg/l  yeast  extract. All three  substrates
           contained equal amounts of carbon.
Results similar to those obtained with a high level of substrates in unpolluted water (Fig. 6} were
obtained with a low substrate level,  shown in Figure 7. In  all cases, this low level of substrate
limited the amount of  DO utilized. Growth factors added in the yeast and beef extracts shortened
the acceleration phase, but the extent of DO utilization with these substrates was less than with
the vitamin-free  casamino acids. This  suggested that one or more amino acids were required by a
large  portion of the bacterial population and  that there was  a  limiting  amount  present in  the
extracts. Similar results were obtained at 0°, 5°, 15° and 20°  C with this low substrate level. Since
these data would be redundant, they have not been shown.

The Effect On DO Depletion When  Nitrogen And Phosphorus Were Added To Subarctic River
Water In The Presence Of Substrates Devoid Of These Nutrients

Ammonia, nitrite  and  nitrate nitrogen  and  orthophosphate  phosphorus concentrations were
determined by chemical analysis each time samples were taken from either location, and the ranges
of values obtained are shown in Table 3. Both ammonia nitrogen and orthophosphate phosphorus
were  increased by domestic pollution.

The results in Figures 8 and 9 indicated that glucose, which contained the same amount of carbon
as the vitamin-free casamino acids control, was poorly utilized  as a substrate for DO depletion in
Chena River  water. Nitrogen and phosphorus, in amounts equal to the  amounts  in vitamin-free

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 82
casamino acids, were added to the river water, which contained glucose. When nitrogen alone was
added to the system, little effect on the DO depletion was observed with either polluted (Fig. 8} or
unpolluted (Fig. 9) water. The same was true for phosphorus in the polluted water. However,
when phosphorus was added to the unpolluted water, DO depletion appeared to be enhanced to
some extent. This suggested that the amount of phosphorus naturally present was a limiting factor.
When phosphorus  and nitrogen were both added, a very marked effect on  DO depletion in the
                                          40  60  6O
                                          TIME (HOURS)
FIGURE?
Relative effect of low levels (substrate being rate limiting) of three complex organic
substrates on dissolved oxygen depletion in unpolluted sub-Arctic river water when
incubated at 10° C. Symbols: o, river water blank; •, 30 mg/l vitamin-free casamino
acids; D, 26  mg/l  beef extract; •, 20 mg/l yeast extract. All  three  substrates
contained equal amounts of carbon.
                                        TABLE  3
                       Chemical Analysis of Water Samples from Two
                               Locations on a Subarctic River
Determination
Dissolved Oxygen
Ammonia Nitrogen
Nitrate Nitrogen
Nitrite Nitrogen
Orthosphate
  Phosphorus
                        Polluted Sample
                           Location3

                         2.5   - 5.9
                         0.40  -0.83
                         0.02  -0.09
                         0.003 - 0.007

                         0.02  -0.08
Range of Values (mg/l/hr)

                  Unpolluted Sample
                      Location11

                     3.5   -8.0
                     0.06  -0.18
                     0.03  -0.12
                     0.001 - 0.004

                     <0.01 - 0.02
     a.   The polluted location was below a reach of the river receiving raw domestic sewage and
         effluents from primary sewage treatment plants. The range of values is from 10 samples
         taken between December 16,1969 and April 7,1970.

     b.   The unpolluted location was  upstream  from any source of domestic or industrial
         pollution. The range of values is from 7 samples taken between December 10,1969 and
         April 14,1970.

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                                                                                 83
                                   40    50     60
                                    TIME (HOURS)
                                               70    80     90     100
FIGURE 8
Effect of glucose on dissolved  oxygen depletion in sub-Arctic river water polluted
with raw domestic sewage and effluents from primary treatment plants. Incubation
at 10° C in the presence and absence of added inorganic nitrogen and phosphorus.
Symbols: o, river water blank; A, 120 mg/l vitamin-free casamino acids as a control;
•, 80 mg/l glucose; D,  80 mg/l  glucose, KH2PO4 (0.33 mg/l phosphorus) and
K2HPO4  (0.33 mg/l  phosphorus); •, 80 mg/l glucose. (NH4)2SO4  (3.33 mg/l
nitrogen) and KNO3 (10 mg/l  nitrogen); A, 80 mg. I glucose, K2HPO4, KH2P04,
(NH4)2SO4 and KNO3 (nitrogen and phosphorus  in same amounts as above). The
glucose,  K2HPO4f KH2PO4, (NH4)2SO4  and  KN03 were added to give the same
levels of carbon, phosphorus, and nitrogen as found in the casamino acids control.

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 84
              20    40
60
80    100    120
 TIME (HOURS)
140    160    180    200
FIGURE 9  Effect of glucose on dissolved oxygen depletion in unpolluted sub-Arctic river water
           when incubated at 10° C in the presence and absence of added inorganic nitrogen
           and phosphorus. Symbols: o, river water blank; A, 120 mg/i vitamin-free casamino
           acids as a control; •, 80 mg/l glucose; A, 80 mg/l glucose, KH2PO4 (0.33 mg/l
           phosphorus) and K2HPO4 (0.33 mg/l phosphorus); Q, 80 mg/l glucose, (NH4)2 SO4
           (3.33 mg/l nitrogen)  and  KNO3  (10 mg/l nitrogen); •, 80 mg/l glucose,  K2HPO4,
           KH2  PO4  and KNO3 (nitrogen and phosphorus in same  amounts as above). The
           glucose, K2HPO4f KH2PO4, (NH4)2SO4 and  KNO3 were added to give the same
           levels of carbon, phosphorus, and nitrogen as found in the casamino acids control.

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                                                                                      85
presence of glucose was observed with either polluted or unpolluted river water. This effect was
more pronounced with the unpolluted (Fig. 9) than with the polluted water (Fig. 8)., because it
altered both the extent of DO depletion and the time span, while only the time span was changed
in the polluted water. These results also suggested that a portion of the bacterial population was
not active  in DO depletion with glucose as the substrate, possibly because the necessary growth
factors were not provided.

The effect  of added nitrogen  and phosphorus on  DO depletion,  with ethyl alcohol (Fig. 10) and
sodium  acetate (Fig. 11} as the substrates, was studied in unpolluted water. The carbon content of
both substrates and the amount of  nitrogen and phosphorus  added were the same as in  the
vitamin-free casamino acids control. Both of these substrates were even more poorly utilized for
DO depletion than was the glucose (Fig. 9) without the addition of  nitrogen and phosphorus.
Again, as with glucose, the addition of nitrogen and phosphorus enhanced the utilization of ethyl
alcohol  and sodium acetate. The DO  depletion with  the vitamin-free casamino acids control was
still greater even though the utilization in the presence of these  substrates was enhanced. This is
added support for the role of growth factors in the metabolic activity of the bacterial population.

Both yeast and beef extracts contained slightly less  ammonia nitrogen than did the vitamin-free
casamino acids. The addition  of ammonia nitrogen had no effect on the utilization of DO with
either extract in polluted or unpolluted water, since  the results were identical to those shown in
Figures 5 and 6.
                                        40   60  80
                                         TIME (HOURS)

FIGURE 10 Effect of ethyl alcohol on dissolved oxygen depletion in unpolluted sub-Arctic river
           water  when  incubated at  10° C  in  the  presence and absence of added  inorganic
           nitrogen and phosphorus. Symbols: o,  river water blank; A, 120 mg/l vitamin-free
           casamino  acids as a control;  •, 60 mg/l  ethyl alcohol;  D, 60 mg/l ethyl alcohol.
           K2HPO4  (0.33 mg/l  phosphorus), KH2PO4 (0.33 mg/l phosphorus), (NH4)2SO4
           (3.33  mg/l nitrogen)  and KNO3  (10 mg/l nitrogen). The ethyl alcohol, K2HPO4,
           KH2PO4, (NH4)2SO4, and KNO3 were  added to give the same levels of carbon,
           phosphorus and nitrogen as found in the casamino acids control.

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  86
                                     20   tO  60  80
                                        TIME (HOURS)
100  120
 FIGURE 11  Effect of sodium acetate on dissolved oxygen depletion in unpolluted  sub-Arctic
             river water when incubated at 10° C in the presence and absence of added inorganic
             nitrogen and phosphorus. Symbols: o, river water blank; A, 120 mg/l vitamin-free
             casamino acids as a control; •, 180 mg/l sodium acetate; A, 180 mg/l sodium acetate,
             K2HPO4  <0.33  mg/l  phosphorus), KH2PO4  (0.33 mg/l phosphorus). (NH4)2SO4
             (3.33 mg/l nitrogen) and KNO3 (10 mg/l nitrogen). The sodium acetate, K2HPO4,
             KH2PO4, (NH4)2SO4  and  KNO3 were  added to give the same level of carbon,
             phosphorus, and nitrogen as found in the casamino acids control.
Effect Of Sewage Treatment Plant Effluents On DO Depletion In  Unpolluted Subarctic River
Water

The  primary sewage treatment plant effluent contained 24  mg/l  ammonia nitrogen, 0.01  mg/l
nitrite  nitrogen, 0.15 mg/l  nitrate  nitrogen,  3.4 mg/l orthophosphate phosphorus and 235 mg/l
chemical oxygen demand (COD). This effluent was added to  unpolluted river water in an amount
which  gave a final COD of 59 mg/l. These results are shown in Figure 12. Oxidizable substrate,
growth factors and  inorganic nutrients  in  the effluent permitted rapid DO depletion  at  all
incubation temperatures. This DO depletion was more rapid than with a high level  of vitamin-free
casamino acids (Fig. 4). Since the indigenous population in  the river  water had  no discernible
effect on DO depletion at any incubation temperature, it appeared that the effluent had a bacterial
population capable of rapid and extensive activity.

The  effect of effluent from an  activated  sludge sewage treatment system on DO depletion in
unpolluted water is shown in Figure 13. Effluent from the activated sludge system operating at 0°
-  1.0° C was added to unpolluted river water, giving a final COD of 16 mg/l. The  results showed
that  DO depletion activity increased with increasing incubation temperature. This suggested that
either a change in growth factor  requirements or different enzyme systems made more substrate
available for utilization at the higher incubation temperatures.  The bacterial population in the river
water appeared to have some effect on the extent of DO depletion at 10° and 20° C, since the rate
and extent of depletion was increased when the effluent was incubated in river water.

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                                                                                       87
                                     40   eo   ao   co
                                        TIME (HOURS)
                                                    120  140  I6O
FIGURE 12  Effect of incubation temperature on dissolved oxygen depletion when effluent from
            the Fairbanks, Alaska  city primary sewage treatment plant was added to unpolluted
            sub-Arctic river water. Symbols:  o, 25% effluent  and 75% river water; •,  25%
            effluent and 75% sterile glass distilled water; •, 25% sterile glass distilled water and
            75% river water.
                               ao  ieo
                                       160  200  240  280
                                         TIME  (HOURS)
                                                        320  360  4W480
FIGURE 13 Effect of incubation temperature on dissolved oxygen depletion when effluent from
            a 0° • 0.5° C bench scale activated sludge sewage  treatment system was added to
            unpolluted sub-Arctic river water. Symbols: A, 25% effluent and 75% river water; o,
            25% effluent and 75% sterile glass distilled water; •, 25% sterile glass distilled water
            and 75% river water.
 Effect Of Incubation Temperature On DO  Depletion In Arctic Water In The Presence Of A
 Complex Organic Substrate

 Vitamin-free  casamino acids at a concentration of 120 mg/l were used as the substrate for DO
 depletion studies in  arctic river water (Sag River). The results, given in  Figure 14, showed a lag
 phase at all incubation temperatures before DO depletion began. The lag phase was extremely long
 at the lower  temperatures, particularly at 0° C. However, the extent of DO depletion did not
 appear to be  temperature dependent.  It has been shown previously (Gordon, unpubl) that the Sag

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 88
                     80  120
                               160 200  240  280    500  540  580  620  660   700
                                         TIME (HOURS)
FIGURE 14  Effect of incubation temperature on dissolved oxygen depletion when 120 mg/1
            vitamin-free casamino acids  were added to unpolluted Arctic river  water. A river
            water blank (o) was incubated atO°, 10° and 20° C.
River had a large population of heterotrophic  bacteria  capable of growth  at low temperatures.
Since only one large volume sample was available from the Sag River, the reason for the extended
lag phase remains to be determined.

The  same substrate  concentration and incubation  temperatures  made it possible  to relate the
results from both the Sag {Fig. 14) and Chena (Figs. 3 and 4) rivers. One outstanding point was the
relative time before the start of DO depletion. There was a lag phase only at the 0° C incubation
temperature with samples from the polluted location on the Chena River, and the lag phase was
apparent only at 0°, 5° and 10° C with samples from the unpolluted location. An extended fag
phase at  all temperatures was observed with samples from the Sag River. A point of similarity with
all samples was that the extent of the DO depletion did not appear to be temperature dependent.

The  results shown in Figures 3. 4 and 14 did not fit either the first or second order kinetic forms,
so a rate constant was  not obtained. Approximate rates (mg/l/hr)  of DO depletion were  obtained
directly from  the depletion curves, and the results are presented  in Table 4. it must be stressed
that these results are approximations and  have value only  in the  context of this study.  It would
seem reasonable to have found the highest rates of DO  depletion with polluted Chena River water.
However, unpolluted Chena River water apparently gave higher rates than the polluted equivalent
at 15° and 20° C. The rates from both Chena River samples were nearly the same at 0°, 5° and 10°
C. The sample from the Sag River gave lower rates at  10°, 15° and 20° C than either Chena River
sample. This suggested  that the bacteria from the Sag  River were more adversely  affected by the
higher incubation temperatures than  those from the Chena River. Additional support for this
suggestion was the  nearly equal rates found at  15° and  20° C with Sag  River water. The results
showed that the source of the sample had little or no effect on the rate of DO depletion at 0° and
5° C. This suggested that all or part of the bacterial population from each  source had the  same
ability to utilize an organic substrate at low temperatures.

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                                                                                      89
                                       TABLE 4

          Comparison of the Rate of Dissolved Oxygen Depletion When a Substrate
                  Was Added to Arctic and Subarctic River Water Samples

Incubation
Temperature                                  Rate of Dissolved Oxygen Depletion  (mg/l/hr)
                                  Subarctic River                            Arctic River
                    Polluted Sample          Unpolluted Sample          Unpolluted Sample
                       Location"                Location0                  Location
    20°                    1.36                      1.73                      0.62
    15°                    0.92                      1.13                      0.65
    10°                    0.63                      0.53                      0.35
     5°                    0.22                      0.26                      0.20
     0°                    0.22                      0.25                      0.20


    a.    120 mg/1 Vitamin-Free Casamino Acids (Difco) was added to each river water sample.

    b.    The polluted location was below a reach of the river receiving raw domestic sewage and
         effluents from primary sewage treatment plants.

    c.    The unpolluted location  was  upstream from any  source of domestic or industrial
         pollution.
                           DISCUSSION  AND  CONCLUSIONS

A subarctic (Chena) river had a population of heterotrophic bacteria capable of growth at 0° C on
a complex medium. With dissolved oxygen (DO) depletion as the measurement, there appeared to
be little metabolic activity in a closed, stationary river water system. When vitamin-free casamino
acids were added  to the stationary  system, there was rapid and  extensive DO depletion at all
incubation temperatures (Fig. 4). The rate of DO depletion appeared to still be increasing at the
lower incubation temperatures when  the oxygen was exhausted, which suggested the maximum
rate had not been reached. Thus, oxygen may have been limiting.

Jezeski and Olsen  (1961) found that shake cultures increased growth rate and maximum growth
level of Pseudomonas fluorescens at 4° and 10° C as compared to stationary cultures. In the shake
cultures, oxygen was no longer a limiting factor, and  the bacterial cells were kept in a constantly
changing  micro-environment  which removed  metabolic end products and brought the cells in
contact  with  new substrate. Such  a  dynamic  system more nearly simulates environmental
conditions in a river than does a stationary system. The indigenous bacteria had the potential for
rapid metabolic activity in a stationary system. Next, a dynamic system must be studied to more
accurately assess the role of  these bacteria  in the natural environment and the effects of added
substrates, such as sewage effluents.

Metabolic activity observed  with the  protein  derivative,  vitamin-free  casamino  acids, as the
substrate was not as rapid as  with yeast or beef extract (Fig. 6). These extracts contained growth
factors and carbohydrates in addition to proteinaceous material. It was apparent that one or more
growth factors were  responsible for the increased metabolic activity. However, it is not known
whether  the growth  factors enhanced the activity  of all or part of the  bacterial population, or

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 90
whether a portion of the population had an absolute growth factor requirement. An understanding
of the role of growth factors is  necessary as an aid in developing design criteria for  sewage
treatment plants that will provide sewage effluents that minimize the demand for DO.

In a review of psychrophilic bacteria,  Ingraham and Stokes (1959) pointed out that they could
carry out nearly all  metabolic activities at low temperatures, but at a slower rate than at higher
temperatures. Several psychrophilic and mesophilic Arthrobacter species were studied for effect of
temperature on growth by Roth and Wheaton (1962). Rather than a sharp cut-off point, there was
a continuous gradation with a decreasing lag phase at 0° C and an increasing one at 37°  C. The
longest lag phase they measured at 0° C was about 300 hours before the start of  fairly  rapid
growth. They  concluded that the number  of generations  of a specific bacterium was not
temperature  dependent,  but the  time to attain  a certain number was  extended  at  lower
temperatures.

The  decreasing rate  of metabolic activity with decreasing  incubation temperature which was
reported  previously (Ingram and Stokes,  1959) appeared to be borne out by the  results reported
here (Table 4). This  was  true with samples from above and below the polluted reach of the Chena
River. Several significant  effects on metabolic  activity in the samples were noted  after the Chena
River had flowed through the polluted reach. The lag phase before the start of DO depletion was
much shorter  (Fig. 3)  than with samples from above (Fig. 4), which resulted  in  a much  shorter
elapsed time from the start of incubation until all of the DO had been utilized. The apparent effect
of growth factors on the  rate of DO depletion was reduced (Figs. 5 and 6), and glucose was more
effectively utilized as a substrate (Figs.  8 and 9). These effects on metabolic activity  indicated that
raw sewage and primary treatment plant effluents added a high level of organic  substrates, growth
factors, nitrogen  and phosphorus  to  the river water. In addition  to the nutrients, the results
presented  in  Figure  12  showed  that  bacteria capable of rapid  metabolic activity  at low
temperatures were present in the primary treatment plant effluent. Because of  these factors, raw
sewage and primary effluents would probably significantly  increase the DO demand  under ice
cover.


McDonald, et al. (1963) found proteolytic bacteria in arctic littoral and marine sediments.  They
found that proteolytic enzymes were highly active at low temperatures and proposed that  these
enzymes  might be significant in protein degradation  in  the Arctic.  Rapid and  extensive DO
depletion was found in Chena  River water at low temperatures with  protein  derivatives as the
substrates. This suggested that proteolysis is one of the major metabolic activities of the bacteria in
the Chena River.

A large variety of proteolytic bacteria  have  been found in sewage treatment systems (Green,
1964). Since proteolytic activity has been found at low temperatures, there are probably similar
bacteria  present in sewage  treatment  systems operating at low temperatures. Support for this
suggestion was obtained from an activated sludge sewage treatment system operating at 0° C. This
system reduced the DO requirements of domestic sewage to a level that appeared to  be of minimal
influence in Chena River water at 0° C (Fig. 13).

Earlier work with pure  cultures of Pseudomonas fluorescens showed that glucose  was  a  poor
substrate for DO utilization at low temperatures (Jezeski and Olsen, 1961) and that the generation
time was much longer than with vitamin-free casamino acids as the substrate (Olsen and Jezeski,
1963). This may have resulted from a change in the metabolic pathway of gluscose utilization at

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                                                                                        91.
low temperatures (Jezeski and Olsen, 1961; Palumbo and Witter, 1969b), or that more glucose was
consumed for cell maintenance  at low temperatures (Palumbo and Witter, 1969b). Inoue, et al.
(1967) found that acetate-oxidizing bacteria were vital in self-purification of rivers.

When  substrates  (glucose,  sodium  acetate and ethyl  alcohol) that did  not contain nitrogen,
phosphorus or growth factors were added to the closed, stationary river water system, a low level
of  metabolic activity resulted. Adding nitrogen and phosphorus resulted in a marked increase in
activity (Figs. 9,  10 and 11). Even with these nutrients present, the  rate of DO depletion was
greater  with the vitamin-free casamino  acids. This suggested that a portion  of  the  bacterial
population either required  additional  growth  factors, or  was  not  capable of utilizing these
substrates. Even though bacteria capable of  utilizing these substrates were present in the Chena
River, activity would probably be at a low level because of the limited amount of nitrogen and
phosphorus present under natural conditions.

Bacteria were found to  have an important role in the cycling  of phosphorus in the aquatic
environment (Philips,  1964),  and both phosphorus and  nitrogen  appeared to  be effective  in
limiting metabolic activity  in the Chena  River  under natural  conditions (Fig. 9). Nitrogen and
phosphorus  present  in raw sewage and  primary  sewage treatment plant effluents  reduced  the
limiting effect of these nutrients (Fig.  8). Therefore, a method must be found to control nitrogen
and phosphorus in effluents entering arctic or subarctic waters. Barth, etal. (1968) demonstrated
that it is feasible to remove both nitrogen and phosphorus on a pilot plant scale using a combined
chemical-biological removal'system. Since several methods are  available (Nesbitt,  1969), the state
of  the art of phosphorus removal is probably much more advanced than nitrogen removal. Perhaps
the initial efforts should be directed toward adapting a phosphorus removal method.

Throughout this  study, nitrogen was supplied  in  the form of ammonia and  nitrate at the levels
present in the vitamin-free casamino acids. It is necessary to determine if the nitrogen form has
any effect, and what concentration is actually required. This should aid  in determining what could
be done to control the effect of nitrogen on receiving waters.

Results obtained with arctic river water were far too limited to be conclusive. However, there are
some general similarities between the  arctic  (Fig. 14) and subarctic rivers (Figs. 3 and 4). More
detailed study is necessary before the effects of pollutants on arctic rivers can be defined.

It is becoming increasingly obvious that the 5 day, 20° C BOD (biochemical oxygen demand) has
very  limited usefulness  in  the arctic  or subarctic because receiving waters rarely reach this
temperature. Previous studies by Murphy  and  Miller (1968), Reid and Benson (1966), and Reid
(1968) showed that a 20 day BOD, incubated at a low temperature with receiving water or seed
culture acclimatized at a low temperature, gave more realistic results with raw sewage. The results
presented here (Figs. 12 and 13) showed that incubation temperature and diluent had an effect on
DO depletion with sewage treatment plant effluents. Therefore, it is suggested that the receiving
water should be  used as the diluent and  the incubation temperature  should be at or  near  the
temperature of the receiving water.

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 92


                                 ACKNOWLEDGMENTS

 Mrs. Becky L. Quimby for her able assistance in the laboratory.

 Mr. Ernest W. Mueller and his staff for providing the chemical data presented here.

 Mr. Michael A. Angelo for assistance in the mathematical treatment of the data.

 Mr. Sidney E.  Clark for help in developing  the equipment used  for  aeration and temperature
 equilibration of the samples.
 Use of product and company names is for identification only and does not constitute endorsement
 by the U.S. Department of the Interior or the Federal Water Quality Administration.
                                      REFERENCES

Adams, J. C. and Stokes, J. L. (1968) Vitamin requirements of psychrophilic species of bacillus, J.
     of Bacteriology, 95, p 239.

American Public Health Association (1965) Standard Methods for the Examination of Water and
     Wastewater, 12th Edition, American Public Health Association, Inc., New York.

Association  of  Official Agricultural  Chemists  (1965)  Official Methods of  Analysis of the
     Association of  Agricultural  Chemists,  10th Edition, Association of Official  Agricultural
     Chemists. Washington, D. C.

Barth, E. F., Brenner, R. C. and Lewis, R. F. (1968) Chemical-biological control of nitrogen and
     phosphorus in wastewater effluent, J. Water Poll. Control Fed., 40, p 2040.

Boyd, W. L. (1958) Microbiological studies of arctic soils. Ecology, 39, p 332.

Boyd, W. L. and Boyd, J. W.  (1967)  Microbiological studies of aquatic habitats of the area of
     Inuvik, Northwest Territories, Arctic, 20, p 27.

Drachev, S. M.  (1964) The oxygen regime and the  process of self purification in reservoirs with
     retarded discharge. Advances  in Water Pollution Research, 1, p 17, The MacMillan Company,
     New York.

Farrell,  J. and  Rose, A.  H.  (1965)  Low temperature  microbiology.  Advances in Applied
     Microbiology,  7, p 335.

Farrell,  J. and Rose, A. H. (1967) Temperature  effects  on microorganisms. Annual Review of
     Microbiology,  21. p 101.

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                                                                                     93
Federal Water Quality Administration  (1969)  FWPCA Methods for Chemical Analysis of Water
    and Wastes, FWQA, Division of Water Quality Research, Anal. Qual. Cont. Lab., Cincinnati,
    Ohio.

Fournelle, H. J. (1967) Soil and water bacteria in the Alaskan subarctic tundra, Arctic, 20, p 104.

Frey, P. J.  (1969) Ecological  changes  in the Chena  River, FWQA Publication, Alaska Water
    Laboratory, College, Alaska.

         Unpubl data, FWQA, Alaska Water  Laboratory, College, Alaska.

Gordon, R. C., Unpubl data, FWQA, Alaska Water Laboratory, College, Alaska.

Green, S. R. (1964)  Proteolysis and proteolytic organisms, In Principles and Applications  in
    Aquatic Microbiology, p 430, John Wiley & Sons, Inc., New York.

Ingraham, J. L. and Maaloe, O. (1967) Cold sensitive mutants and the minimum  temperature of
    growth of bacteria. In Molecular Mechanisms of Temperature Adaptation, p. 297, American
    Association for the Advancement of Science, Washington, D. C.

Ingraham, J. L. and Stokes, J. L. (1959) Psychrophilic bacteria. Bacteriological Reviews 23, p 97.

Inoue.  Z.,  Honda, A. and  Ishii, R.  (1967) The  role of acetic  acid degrading bacteria  in
    self-purification of freshwater streams, J. of Fermentation Technology, 45, p 570.

Jezeski,  J. J, and Olsen, R,  H. (1961) The activity  of enzymes at low temperatures, p 139,
    Proceedings of the Low Temperature Microbiological Symposium, Campbell Soup Company,
    Camden, New Jersey.

Lotspeich, F. B., Unpubl data, FWQA, Alaska Water Laboratory, College, Alaska.

McDonald,  I. J.,  Quadling, C.  and Chambers, A. K.  (1963) Proteolytic activity of some cold
    tolerant bacteria from arctic sediments, Canadian J. of Microbiology, 9, p 303.

Miller, A. P. (1967) The biochemical  bases of psychrophily  in microorganisms, a review, Institute
    of Water Resources, University of Alaska, College, Alaska.

Mueller, E. W., Unpubl data, FWQA, Alaska Water Laboratory, College, Alaska.

Mulder, E. G. (1964) Arthrobacter, In Principles and Applications in Aquatic Microbiology, p 254,
    John Wiley & Sons, Inc.,  New York.

Murphy, R. S., Asce,  M.  and Miller, A. P.  (1968) Waste induced oxygen uptake of an Alaskan
    estuary, J. Sanitary Engineering Div., A.S.C.E., 94, p 345.

Nesbitt,  J. B. (1969)  Phosphorus removal -  the state of the art, J. Water Poll. Cont. Fed., 41, p
    701.

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 94
Olsen, R. H. and Jezeski, J. J. (1963) Some effects of carbon source, aeration, and temperature on
     growth of a psychrophilic strain of Pseudomonas fluorescens, J. of Bacteriology, 86, p 429.

Palumbo, S. A.  and Witter, E. D.  (1969a) Influence  of temperature  on glucose  utilization by
     Pseudomonas fluorescens, Applied Microbiology, 18, p. 137.

                  (1969b) The influence of temperature on the pathways of glucose catabolism
     in Pseudomonas fluorescens, Canadian J. Of Microbiology, 15, p 995.

Pereira,  J. N. and Morgan, M. E. (1957) Nutrition and physiology of Pseudomonas fragi, J. of
     Bacteriology, 74, p 710.

Philips,  J.  E.  (1964) The ecological role  of  phosphorus in waters with  special reference to
     microorganisms. In  Principles and Applications of Aquatic Microbiology, p 61, John Wiley &
     Sons, Inc., New York.


Prince, H. N., Beck,  E. S., Cleverdon, R.C. and Kulp, W. L. (1954) The flavobacteria, I. nutritional
     requirements, J. of  Bacteriology, 68, p 326.

Reid, L. C., Jr. (1968) Design and operation considerations for aerated lagoons in  the arctic and
     subarctic, Arctic Health Research Center Rept. No. 102.

Reid. L. C., Jr. and Benson, B. E. (1966) Observations on aerated sewage lagoons in arctic Alaska,
     presented at the Eighteenth Annual Convention  of the Western Canada  Water and Sewage
     Conference, Regina, Saskatchewan, Canada.

Roguski, E. (1967)  Inventory and cataloging of the sport fish and sport fish waters in the interior
     of  Alaska, Alaska Department of  Fish and Game, Federal Aid in Fish Restoration. Annual
     Report of Progress, p 243.

Roth, N. G. and Wheaton, R. B.  (1962)  Continuity  of psychrophilic and mesophilic growth
     characteristics in the genus Arthrobaeter, J. of Bacteriology, 83, p 551.

Schallock, E. W., Unpubl data, FWQA, Alaska Water Laboratory, College, Alaska.

State of Alaska (1967) Water Quality Standards for Interstate Waters Within the State of Alaska
     and a  Plan  for the  Implementation and Enforcement of the Criteria, Department of Health
     and Welfare, Juneau, Alaska.

Stefaniak, O. (1968) Occurrence and some properties of aerobic psychrophilic soil  bacteria. Plant
     and Soil, 29, p  193.

Stokes,  J. L. and Redmond, M. L. (1966) Quantitative ecology of psychrophilic microorganisms,
     Applied Microbiology, 14, p 74.

Straka,  R. P. and Stokes, J. L. (1960) Psychrophilic bacteria from Antarctica,  J. of Bacteriology,
     80, p 622.

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                                                                                     95
Wuhrmann,  K.,   Ruchti,  J.,  and  Eichenberger.   E.  (1966)  Quantitative  experiments  on
    self-purification with pure organic compounds, In Advances in Water Pollution Research, 1, p
    229., Water Poll. Cont. Fed., Washington, D. C.

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          PREDICTION  OF DISSOLVED OXYGEN  LEVELS  IN  THE
                 SOUTH  SASKATCHEWAN  RIVER  IN  WINTER
                                   Robert C. Landine
                                   INTRODUCTION

Water pollution  is a problem of growing importance. The general public is becoming increasingly
concerned over the desecration of  our natural resources  through  pollution. In Canada, the
Provincial and Federal Governments have acknowledged the need for preserving and upgrading our
water resources and have introduced more effective legislation for pollution control.

The discharge of municipal and industrial waste water effluents into a river may lead to excessive
demands on  the  dissolved  oxygen  (DO) resources  of  the river. To  maintain  the  river in a
satisfactory state and in proper ecological balance it is necessary to prevent the DO concentration
from falling too low.

The  DO concentration is regarded as  one of the most important parameters for measuring or
assessing the degree  of  pollution  in a river. Water  pollution control  agencies always include
minimum allowable DO concentrations in their list of pollution control parameters.
               UNITED STATES OF AMERICA
                FIGURE 1   Location of south Saskatchewan River in Canada
                                           96

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                                                                                       97


The 00 concentration  at any point along  a river depends on  the  rates of oxygen supply and
demand. The respiration oxygen demand is  counterbalanced  by the supply of oxygen  through
atmospheric reaeration and photosynthesis. The supply and demand of oxygen are related through
the complex phenomenon of oxygen balance which is determined by an interplay  of  many
physical, chemical and biological factors. Another important reason  why the DO parameter is so
frequently  used  in pollution control work is that it is possible to  use mathematical equations or
models  to  represent  (approximately) the various forces operating  in  the oxygen balance. It is
possible to formulate equations for predicting the DO  level at any point along a water course
under various conditions.

The opportunity for renewal  through reaeration and photosynthesis  is greatly, if not entirely,
reduced during the winter ice  cover period which lasts five to six months in northern climates. A
blanket of  ice and snow over the water shuts out the light, thereby  denying photosynthesis. The
ice also prevents  natural reaeration of the water.

From the above  paragraph it follows that the oxidation of organic matter in ice covered rivers will
result in a  progressive reduction in the DO level as the river flows downstream. Therefore, if the
oxidation rate is sufficiently high and the river is long (long time of passage) the DO concentration
will eventually fall to undesirable levels. Another point is that the  flows in unregulated streams in
regions with prolonged frost periods tend to be minimal during winter. Therefore, the most critical
DO levels may be experienced in winter rather than in summer. Almost all cases reported  in the
literature are for critical conditions occurring in summer.

With the distinct possibility  of minimum DO levels occurring in winter coupled with the need for
better methods  of predicting  DO levels under ice conditions, an investigation was made into the
prediction  of DO levels in a prairie stream under such conditions. The study was problem-oriented;
it was conducted from the viewpoint that the results should be useful to a water pollution control
agency.

The South Saskatchewan  River  was selected for  a case study.  It is a fairly large river, with an
average annual flow of approximately 10,000 cfs, being one of two  major branches which combine
to form the Saskatchewan River. The Saskatchewan River System, which is 1,300 miles long, has
its headwaters in the Rocky Mountains near the  Alberta-British  Columbia  border  and  flows
easterly through Alberta, Saskatchewan and into Lake Winnipeg, in Manitoba, as shown in Figure
1. From Lake Winnipeg, which is a large lake with  an  area of 9,000 mi2, the water  flows into
Hudson Bay via the Nelson River. The Saskatchewan-Nelson River System is  1,600 miles long,
being the second longest in the country, and forms part  of the Hudson Bay drainage area basin of
1,421,350 mi2, the largest in Canada.

The South Saskatchewan  River  is 900  miles long from  the headwaters to the junction with the
North Saskatchewan River, approximately 20 miles east of Prince Albert, Saskatchewan. From the
profile  shown  in  Figure  2 it is apparent  that  the river channel  gradient is moderate  across
Saskatchewan, being approximately 1.8 ft per mile.

The South Saskatchewan  River was selected for  a case study because 1) it is one of the most
important rivers in the region  and one with which the writer had  previous experience and 2)  it was
very  convenient, passing  by  the University of Saskatchewan in  Saskatoon.  As it turned out,
however, there were some aspects which rendered  this river something less than an ideal choice.

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98
                                          Soft
                                        SosMchewon
                                             Dtefenboker
           "eOO—IKDO   1006  900   800   700   €00~
                Distance above Lake Winnipeg in miles

      FIGURE 2   Profile of Saskatchewan River system from headwaters to Lake Winnipeg


Diefenbaker  Lake, the large reservoir  created  by Gardiner Dam, formed  a  logical  upstream
boundary point, and the confluence with the North Saskatchewan River. 213 miles below the
Dam, was the downstream control point. This 213-mile reach of river received pollution loadings
from municipalities and industries and much greater loadings were anticipated in the future.

The 213-mile reach selected for a case study was subdivided into 11 reaches as shown in Figure 3.

                    DEVELOPMENT OF  DO  EQUATIONS (MODELS)

Ideally, a model should be developed from basic considerations, checked against field observations
and modified so that it will reproduce an existing situation. Then, presumably, the model could be
used to predict what would  happen to the DO profile if certain  changes, such as river flow and
waste loading, occurred in the river system.

The great amount  of human  and financial resources that would have been required precluded the
possibility of evaluating the various factors and coefficients from actual field surveys. Therefore, it
was decided that the coefficients would have to be determined from a literature search supported
by laboratory investigation and field surveys.

Time does not permit a description of the laboratory experiments conducted and the treatment of
data resulting therefrom. Only the pertinent results will be referred to as required in discussing the
oxygen balance situation for each reach.

Two worst winter situations were considered, viz., (1) future and (2) the conditions existing in
1968-69.  Only the latter case will be considered in  this paper. By worst  situation is meant a
prolonged period of subzero weather coupled with low barometric pressure and calm conditions.

Two different river flows were considered,  4,500 cfs  and 11,000 cfs. A flow of 4,500 cfs was
possible and would occur when one of the three turbines was operating at the hydroelectric station
at Gardiner  Dam;  this would be a minimum winter flow. A flow of 11,000 cfs occurs when all

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three turbines are in operation. Also, a flow  of 11,000 cfs was being released from Gardiner Dam
at  the  time the  writer  made a  field survey  to check  the  DO level, and  other parameters,
downstream from the  Dam. It was therefore  useful to include a flow of 11,000 cfs {although such
a high flow would not produce a worst  condition)  so that the predicted DO profile could  be
checked against the observed profile. There were no  tributaries and, thus, the same flow applied
over the entire reach.

The input waste loadings and station mileages are given in Table 1.

A discussion of  the important factors considered in developing the equations to calculate the DO
profile is given below.

                                  INITIAL CONDITIONS

The initial DO concentration of the water entering the river at the exit from the Dam was taken as
11.5 ppm, the value observed on two occasions.

The initial value of the equilibrium saturation value for oxygen  dissolved in water at 0°  C was
taken  as  14.63  ppm  based on the data  presented  by Montgomery, et al.  (1964). Only one
temperature was used  as it was assumed that the water temperature in both the open water reaches
and the ice covered reaches could be taken as 0° C. Only a  minimal error was inherent in this
assumption. A  station pressure correction was  required. Based  on  observations made by the
                                                            NBNWN
                                     PWNCE
                                     ALBERT
                                                      Station
                                                   •  For ry (name as show)
                                                   3Om MM below Gardimr Dam
                                                      R««ch rutter
                                                       l"«20mil»«
                                                  UNITED STATES OF AMERICA
                        COTEAU CREEKf
                        POWER STATIC
                             GARDINER DAM
: WEFENBAKER
FIGURE 3   South  Saskatchewan   River  from  Gardiner  Dam  to  confluence  with  North
            Saskatchewan River

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 100


 Saskatchewan Research  Council  (1969)  a typical winter low pressure  would be  698 mm of
 mercury. No allowance was made for the differences in station pressure due to the difference in
 elevation of the open water reaches at the Dam and 70 miles downstream at Saskatoon. The
 difference in station pressures at the two locations was so small that it was satisfactory to consider
 only one saturation value, i.e., 14.63 x 698/760 = 13.45 ppm for both locations.
                                        TABLE 1

                           Station Description and Waste Loadings
                            Station          Reach          Station          BODS Input in
 Station Name              Number         Number         Mileage         Pounds Per Day

 Gardiner Dam                 1                              0.0                  0
                                              1
 End Open Water               2                              5.0                  0
 Outlook                      3                             18.5                280
                                              3
 Q.E. Power Station            4                             71.5                 0
 Weir Upstream                5                             75.9                 0
 Weir Downstream             6                             75.9                 0
                                              &
 Present City Outfall            7                             76.7              30,000
 IPCO-Armour                 8                             80.9                300
                                              8
 Clarkboro Ferry               9                             93.9                 0
                                              ft
 Gabriel's Perry                10                            124.0                0
                                              10
 St. Louis                      11                            155.0               40
 Weldon Ferry                 12                            202.0                0
 Reach 1, Gardiner Dam To End Open Water, Mile0.0 To 5.0

 The river remains open, even during the coldest weather, below Gardiner Dam as a result of the
 water being discharged from the hydroelectric station at the Dam.

 The lowest rates of reaeration would occur during low pressure, calm conditions. It was assumed
 that in the worst situation both of these conditions could occur in the open water reach 1 and
 again when the corresponding volume of water arrived at the open water reaches in Saskatoon.

The minimum area of open water exposed to the atmosphere would occur at the end of a
prolonged period  of subzero weather. Under these conditions it was estimated that the river would
be open over the entire channel width for a distance of 5 miles below the Dam.

The following equation developed by Owens, et al. (1964)

                                  k2 = 9.41V°-67rf1-85                               <1)

     where k2  = reaeration coefficient day , base 10

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                                                                                     101


        V = river velocity, fps

        h = river mean depth, ft

was used to calculate the reaeration coefficient. No reduction was made for the effect of dissolved
salts,  detergents or  other  contaminants since  the concentration of all of these would be low,
resulting in a negligible correction to k2.

As is evident from Equation 1, k2 is a function of velocity and depth. Since the input data was in
terms of flow,  Q,  rather than h  or V,  it was necessary to express the latter two variables as a
function of Q. By plotting the data presented by Tywoniuk (1969) the following equations of best
fit were derived for reach 1

                                      V =  0.11Q0'32                                   (2)

and
                                     h  = 0.072Q0'47                                  (3)
Likewise, the data given by Schriek (1963) was used to derive the following equations for reach 4,
which was partly ice free

                                      V =  1.55Q0'77                                   (4)

                                     h =  3.1 OQ°-095                                  (5)

It  may  be noted  here that a  relationship giving k2 as a function of Q may be  obtained by
substituting  Equations 2 and 3, or 4 and 5, into Equation 1. This will result in the following
equations for reach 1 and reach 4

                                 k2 =  286Q'0'67 (reach 1)                              (6)

                                k2  = 0.015Q0'34 (reach 4)                              (7)
                                                                               •J/o
From Equation 6  it is apparent that for reach  1  k2 is inversely proportional to Q   , i.e., k2
increases as Q decreases which is very helpful from the water quality point of view. However, the
opposite situation is true for reach 4 which is atypical due to a weir located at the downstream end
of the reach. In this reach the reaeration rate increases as the flow increases.

Past  experience (Lackie and Sparling, 1955;  Sparling, 1957; Bouthillier, 1968; SWRC, unpubl;
Landine, 1962) with prairie rivers under ice  cover conditions has shown that there is always a
certain background or residual  BOD5 of the order of 1 to 2 ppm, in waters far removed from
significant waste water discharges. For example, the  BODS  of South Saskatchewan River water
upstream from Saskatoon was  1.0 ±  0.8 ppm (based on 18 samples collected in the months of
December to February from 1957 to 1969). The only significant sources of municipal  or industrial
pollution were located hundreds of miles upstream.

The explanation of a residual BOD is believed to be related mainly to the slow oxidation of humus
and,  to a lesser degree, to the oxidation of anaerobic end products.  Humus refers to  that portion

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102


of the organic matter that is very resistant to biological  decomposition and could  yield an
essentially constant daily BOD for several days if the amount of humus were sufficient and the
period of time involved not excessive. Periods of several months have been reported for complete
stabilization of polluted river water even at the normal temperature of 20° C (Gannon, 1963;
Garneson, 1958).
The humus material has its origin in 1) the waste water effluents discharged from  industries and
municipalities  in  Alberta (mainly) and Saskatchewan  and 2) the variety of  organic materials
entering the river  through land drainage. Land drainage  occurs only during summer. However, due
to the long  flow-through time in Diefenbaker Lake {1  year  storage  capacity)  the effect  is felt
throughout the winter period both in the lake and in the water released from it.

There would be  a  certain  amount of anaerobic  decomposition in the vicinity of the benthic
growths or  muds; this would be particularly true in the lake. The oxidation  of anaerobic end
products creates an oxygen demand.

The residual oxygen demand (ROD) was treated as a constant demand, in ppm per day, applied
over the entire 213 mile reach. The magnitude of  ROD was obtained from the  above mentioned
BODS @ 20° C, (i.e. 1.0 ± 0.8 ppm) as follows

                                                BODS @ 20° C
                             ROD  ppm/day =  	                        (8)
                                               5 days x  FACT
                                                                         r»o
 where FACT is the factor for converting from BODS  @ 20  C to the BODS @ 0 C for polluted
 river water. From experiments conducted by Landine (1970) it was found that the  magnitude of
 FACT was between 3.0 and 3.5 for polluted river water samples. From Equation 8 the mean value
 of ROD was 0.062 ppm per day; the upper and lower values were 0.120 and 0.011 ppm per day
 respectively.
 There were no municipal or industrial discharges in reach 1.

 There was no need to consider organic toad contributions due to local run-off along the entire 213
 mile reach because there is no run-off during severe winter conditions.

 Photosynthesis was assumed to be insignificant in the oxygen economy of the river in the open
 water reaches as well as the. ice covered reaches. This  assumption was believed to be  reasonable in
 view of the low temperature, the few hours of daylight, and the low intensity of sotar radiation in
 winter. Table 2 illustrates  that the  solar radiation is much lower in winter than in summer in the
 area.
                                        TABLE 2

                         Solar Radiation at Saskatoon. 1955 to 1967
                              (Saskatchewan Research Council)

 Jan.     Feb.    Mar.    Apr.    May   Jun.    Jul.    Aug.    Sept.    Oct.    Nov.   Dec.
 102*    199    326     414     508    544    568     466     326    197    103     74
 Hie average annual total = 115 kilolanglies
 *  Units are langlies/day, equivalent to g cal/cm2  day.

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                                                                                   103


After evaluating the various factors of importance in reach 1, the DO equation was written. The
deficit  at the end of reach 1 is a function of two forces, viz.,  1) reaeration and 2) the constant
ROD rate. The differential equation may be written as

                                  dDt
                                        =  -K2Dt+ROD                               (9)
                                   dt           T


    and integrated to yield

                           Dt =  DQe-K2t  + ROD(1 -e'^VlCa                       (10)

    where

    Dt = DO deficit at time t, i.e., at end of reach,

    DQ =  DO deficit initially, i.e., at beginning of reach,

    t = time of flow in reach in days, obtained from  Equation 2 and 4. (For ice covered reaches
the flow time was increased by 30% to allow for the reduced velocity of flow.)

    K2 =  reaeration coefficient, day" , base e, and

    ROD = constant residual oxygen demand rate @ 0° C, ppm/day.

It  was  unnecessary to write a partial differential equation because with no  photosynthesis there
would be no diurnal  fluctuation in the DO concentration; also, the waste loadings were treated as
constant throughout  the day. A term for dispersion was also neglected; dispersion has a negligible
effect on the calculated DO profile in freshwater streams (Dobbins,  1964).

Reach 2, End Open Water To Outlook, Mile 5.0 to 18.5

There was no reaeration and no waste loading in this reach. The change in DO concentration was a
function only of ROD. Equation 11 was used  to calculate the deficit at the end of reach 2

                                  Dt = DQ + ROD(t)                               (11)

where each term is as defined previously; a complete list of symbols may be found in Appendix 1.

Reach 3, Outlook to Queen Elizabeth Power Station, Mile 18.5 to 71.5

Since organic matter  will remain  in suspension if the stream velocity is more than 1.0 fps (Imhoff,
et  al., 1956) it was assumed that sludge deposits  need  not be considered in this river in which the
velocity exceeds 1 fps. Furthermore,  most of the  solids  which would settle out  are removed in
primary sedimentation and no  waste  water may be discharged without  first receiving at least
primary sedimentation or its equivalent (SWRC, 1967).

A small amount of municipal waste is contributed by the town of Outlook.

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104
The forces causing the DO deficit to increase in this reach are the ROD and the first-order BOD
arising from  the  Outlook sewage discharge. Based on field and laboratory tests conducted  by
Landine (1970) there was no need to allow for a nitrification oxygen demand because nitrification
did not occur at 0° C.

The oxygen demand due to the waste  water discharge may be calculated from Equation 12 which
is the usual first-order BOD equation.

                                    yt = L  d-e-'V)                                (12)

     where y = oxygen demand after t days, in ppm,

        L = ultimate first-stage BOD, ppm,

        K. = first-order  BOD rate constant, day  , base e.

The sequence of calculations was as follows:

(1) the waste discharge  in Ib BODS @ 20° C per day (raw data, see Table 1) was converted to ppm
BOD5 @ 20° C in the river by dividing by 5.38Q;

(2) the river BODS  @ 20° C was converted to a BODS @ 0° C by dividing by FACT for  which
values of 3.0 and 3.5 were used;

(3) the river  BOD5 @ 0° C was converted to an ultimate first-order BOD at 0° C by Equation 12;

(4) The ultimate BOD from step (3) was added to the ultimate BOD remaining at the end of the
previous reach (which was zero for reach 3 but not for  subsequent reaches) to get the total
ultimate BOD @ 0° C at  the beginning of the reach;

(5) the BOD in the reach was calculated by Equation 12,

(6) the BOD calculated in step (5) was subtracted from the total ultimate BOD at the beginning of
the reach to calculate the ultimate BOD remaining at the end of the reach.

To do step (3) above it  was necessary  to know the value of  KI . The exact value of Kt in the river
was not known. To overcome this problem a range of  Kt values, from 0.02 to 0.6 day"1, was used
in calculations. The lowest value 0.02, is very  low and approximates a linear or constant oxygen
demand rate whereas 0.6 is believed to be as high as can be expected. Bouthillier (1968) reported
that the  oxidation rate  constant may be as high as 0.6 in  the North Saskatchewan River  below
Edmonton; Cameron (1967) reported the presence of slimes on  the bottom in this reach  which
could have accounted, in part at least, for the high rate of oxidation.

The following equation was used to caluclate the DO deficit at the end of reach 3

                             Dt = DQ +  ROD(t) + YREACH                         (13)

where YREACH = first-order BOD exerted in the reach due to waste water contributions.

-------
                                                                                     105


Reach 4, Queen Elizabeth Power Station to Weir, Mile 71.5 to 75.9

The cooling water from two power stations maintains a strip of open water along one side of the
river in  this reach. The width of the open water strip depends on such factors as the river flow,
duration of severe cold spell and distance below cooling water discharge point. It was estimated
that under  the worst conditions assumed for this study 15% of the river channel would be ice free.

This reach was treated as two rivers flowing side by side separated by an imaginary wall to prevent
mixing back and forth. Since the reach was just 4.4 miles long with 85% of the channel width
covered  with ice the above assumption was believed to be reasonable.

Reaeration, first-order BOD and  ROD were  the important factors considered  in the open water
river. The differential equation was

                                dDt
                               	  = KiL  +  ROD  -K2Dt                           (14)
                                dt                         T

    which may be integrated to

                           if t    k- i      if  *    \f t    RO°        \f t
                D   = D  e~N2t +  NILO (e   jt - e~N2T) +	 (1  -e~N2T)            (15)
For the  ice covered  strip of river the forces considered were ROD  and first-order BOD, and
Equation 13 was used to calculate the deficit at the end of the reach.

Reach 5. The Weir, Mile 75.9

The amount of aeration realized at this ogee-shape weir was calculated by means of Equation 16,
after Gameson, et al. (1958).

                              r = 1  + 0.11ab{a + 0.046T)ht                           (16)

     where r = ratio of DO deficit above and below weir,

        a = coefficient dependent on nature of water,

        b = coefficient dependent on nature of weir, and

       ht = fall height at weir in feet.


It was  estimated  that  the value of a  would  be  1.25 because the  river was 'clean' at this point.
Values of the coefficient b for an ogee-shape weir were not found  in the literature; two alternate
values, 0.5 and 0.75, were estimated for the value of b in the computations.

The water fall  height, ht> must be known to  use Equation 16. It was found that a semiiog plot of
h  versus Q linearized (Fig. 4) to yield the equation

-------
 106
                  !
IU
8
6
4
?
— *-

Z

T-
/
h=K)x

	 .

o-aii

s*-^
I4xl0'


' 	 j
4Q


	 -.
Reduc
totx*
effec
COVft

•— — ..

	
ed fall due .
*water /
t of ice -/
r dowr
exreurr

                                  4     6    8    10    12    14    16
                            Discharge x  IO"3  cubic feet per second

                           FIGURE 4  Fall height at Saskatoon Weir
                                 ht  = 10x 10
                                             -0.134X 10"4Q
(17)
 Equation 17 was based on data for open water conditions and a correction was necessary to allow
 for the reduced fall height due to the backwater effect of the ice cover below the weir. Limited
 field observations suggested a correction of minus 2 ft so that the equation used to calculate ht as
 a function of Q was
                                                      '4
                               ht =  10x10-°-134x10'Q-2

 Reach 6, Weir To Present Saskatoon Outfall, Mile 75.9 To 76.7
(18)
 It was estimated that the river would be 100% ice covered at mile 76.7 and that 10% of the river
 channel width would be open water in  reach 6. Since the flow time in this reach was very small,
 the differential equation could be left in the differential form, without introducing serious error,
 to calculate Dr The forces considered  were (1) ROD, (2) first-order BOD and (3) reaeration (in
 the open water strip). The equation used was
                          dDt  = KjLdt -  0.1K2D  dt + ROD dt
(19)
where dD  is the change in DO deficit in passing through the reach during a flow time equal to dt.

Reach 7,8, 9, 10 & 11, Mile 76.7 To 213

All of these reaches were treated in the same fashion because  they were completely covered with
ice. Waste loadings were considered when necessary. (See Table 1 for amount and  location.) The
two factors of significance were first-order BOD due to waste water effluents and ROD; Equation
13 was used to calculate the deficits at the end of each reach.
The  prediction of the  DO profile along the  213 mile reach was done  with  the  aid of a digital
computer.

-------
                                                                                   107
            DISCUSSION OF COMPUTER SOLUTIONS OF DO EQUATIONS

It was not possible to include all  of the computed output as this involved several hundred lines;
therefore only a few selected iterations have been included to illustrate the main points of interest
as discussed below.

To check the effect of changing the variables Q, FACT, b. K, and ROD, a suitable range of values
was used for each one. This was written  into the computer programs, using a nest of DO loops,
resulting  in many  iterative calculations for the various combinations.  By scanning through the
output (which  involved less than 2 min. computer time) the reader was quickly able to determine
which factors had the greatest significance in regard to the minimum DO concentration. This was a
low cost and rapid method of evaluating numerous alternatives.

The first point of interest centered around the question of whether  or not the predicted profile
agreed with the observed profile.

The output showed that, when Q = 11,000 cfs, ROD = 0.011 ppm/day, FACT = 3.0 or 3.5, b = 0.5
and for any value of K| from 0.02 to 0.6 day"1, the calculated DO concentration at station 12*
was 12.0 ppm, which agreed very closely with the value of 11.9 ppm found on March 4, 1969. For
the same conditions, except with  ROD changes from 0.011 to 0.062 and 0.12, the calculated DO
concentration  at station  12 was 11.65 and 11.3 ppm respectively. The predicted values for the
three different values of ROD and  the observed values are shown in Figure 5.

At first glance it appeared that the predicted profile was poorer for the higher values of ROD (i.e.
0.062 and  0.12), considering the furthest  station downstream as the  governing or most critical
point.  However, a  closer look showed that the predicted profile downstream from Saskatoon
approximately paralleled the  observed profile for  the case where  ROD =  0.12 ppm per day,
suggesting that this upper value of ROD was the most appropriate one to use.

The discrepancies  between the predicted and  observed concentrations (which were 0.8 ppm or
less) would have been reduced if the field survey could have been made under the same conditions
as were assumed for the model. For example, due to the  mild weather prevailing during the field
survey (March 4 and 5, 1969) the area of  open water in reaches  1,4 and 6 was greater than for the
worst conditions assumed in the model. Also, instead of the assumed calm conditions, there was a
breeze ranging from 5.9 to 22.0 mph (mean daily), prevailing for the period February 22 to March
5, 1969  (SRC, 1969). The effect of the wind would have been to increase the reaeration rate, a
phenomenon which has  been reported by others  (Anon.,  1964; Bohnke,  1966).  Finally, the
barometric pressure was 15 to 28 mm of mercury greater over this same period than was assumed
in the model. All three of the above factors resulted in higher reaeration rates than for the assumed
conditions in the model and thus helped  to explain why the observed concentrations were higher
than the predicted DO concentrations.

Based  on the  above mentioned results, it was felt that the oxygen balance forces and equations
employed were sufficiently representative to be useful in making predictions for this river.
 *Station 12 was at Weldon, 202 miles below Gardiner Dam, the last sampling station before this
 river flowed into the Saskatchewan River.

-------
108
A number of conclusions or deductions could  be made from the computed  output for winter
conditions.

(1) The magnitude of the value employed for ROD had a more pronounced effect on the results
than  did  the  magnitude of K,.  For example, for the minimum flow situation of 4,500 cfs,
changing  ROD from 0.011 to 0.12 changed  the  DO concentration at station 12 from  11.93 to
10.98 pprn, i.e., 1 ppm, whereas changing K, from 0.02 to 0.6 changed the concentration from
11.93 to 12.02 ppm, i.e., 0.1 ppm.
(2) The magnitude of K! had  little effect on YREACH and, consequently, on the DO profile. As
illustrated in column 15 of Table 3, when  the other variables were held constant, changing Kj
from  0.02 to 0.60 day   resulted in the sum of the first-order BOD changing from 0.53 to 0.43
ppm which  is minor. From column  13 it  can be seen that the value of the ultimate BOD at the
beginning of a  reach is much  higher for  the case  of  K!  = 0.02 than for K,  = 0.60. However,
YREACH changed only slightly because a high value of ultimate BOD was used in conjunction
with a low value of K, to calculate YREACH (using Equation 12) and vice versa, which produced
a compensation effect. This suggested that it is not necessary to have an  'exact' value of KI for
calculating the  first-order  BOD in the river provided  that the BOD5  @ 0° C of the waste water
loadings are known.

(3) The  oxygen added in  open water reaches and at weirs is highly significant in the oxygen
economy  of ice covered rivers. This affords an opportunity for the oxygen concentration to be
increased  considerably in a short time. The oxygen  thus added becomes available for the slow
oxidation of organic  matter in subsequent ice covered reaches.
          I
          i
 FIGURES
--

2
-



/ 	







r-Stopeporc
\ ROD=(

	 =


X
0
— &
O


ate) 10
)062
	 1-
	 o-
==£

Open water
:brtiy open <
Complete ice
Observed D
Predated D
Predicted D
Predicted D


	 — . *~
=£=£=
Aeration at
Saskatoon
Weir


1
r-C, =13.45 ppm (mode*

— -_.
~~-^*



rObserved



^
•ater
cover
0 concentrator Mar* 4-5, 1969
0 cone entroti on ROD = 0.01 1 ppm/Jay
0 concentration ROD = OO62 ppm/Wo
0 concentration ROO=O.I2Opprn/da)



-* 	
*-°— ^.

-lee-cover
assumed 1

y



— 	 •<
	 	 -,

>ottern
x mode)


0 25 50 75 100 125 150 175 2CX
                      River miles below Gardiner Dam

Comparison of observed and calculated DO levels for winter conditions, Q = 11,000
cfs.

-------
                                                      TABLE 3


                                  Partial Computed Output for 1968-69 Winter Conditions
1
STA
DK =
0.0
5.0
18.5
71.5
75,9
75.9
76.7
80.9
93.9
124.0
155.0
202.0
DK =
0.0
5.0
18.5
71.5
75.9
75.9
76.7
80.9
93.9
124.0
155.0
202.0
2
I
0.02
1
2
3
4
5
6
7
8
9
10
11
12
0.60
1
2
3
4
5
6
7
8
9
10
11
12
3
BOD

0.
0.
280.
0.
0.
0.
30000.
300.
0.
0.
0.
0.

0.
0.
280.
0.
0.
0.
30000.
300.
0.
0.
0.
0.
4
DK

0.02
0.02
0.02
0.02
0.02
0.02
0.02
0.02
0.02
0.02
0.02


0.60
0.60
0.60
0.60
0.60
0.60
0.60
0.60
0.60
0.60
0.60

5
ROD
ROD
0.011
0.011
0.011
0.011
0.011
0.011
0.011
0.011
0.011
0.011
0.011

ROD
0.011
0.011
0.011
0.011
0.011
0.011
0.011
0.011
0.011
0.011
0.011

6
BWEIR
= 0.011
0.50
0.50
0.50
0.50
0.50
0.50
0.50
0.50
0.50
0.50
0.50

= 0.011
0.50
0.50
0.50
0.50
0.50
0.50
0.50
0.50
0.50
0.50
0.50

7
FACT

3.0
3.0
3,0
3.0
3.0
3.0
3.0
3.0
3.0
3.0
3.0


3.0
3.0
3.0
3.0
3.0
3.0
3.0
3.0
3.0
3.0
3.0

8
C

11.50
12.09
12.09
12.06
12.08
12.51
12.52
12.50
12.43
12.29
12.15
11.93

11.50
12.09
12.09
12.06
12.08
12.51
12.52
12.46
12.33
12.16
12.08
12.02
9
D
FACT
1.95
1.36
1.36
1.39
1.37
0.94
0.93
0.95
1.02
1.16
1.30
1.52
FACT
1.95
1.36
1.36
1.39
1.37
0.94
0.93
0.99
1.12
1.29
1.37
1.43
10
V
= 3
1.10
1.10
1.10
0.68
1.10
1.10
1.10
1.10
1.10
1.10
1.10

= 3
1.10
1.10
1.10
0.68
1.10
1.10
1.10
1.10
1.10
1.10
1.10

11
H
.0
3.91
3.91
3.91
6.89
3.91
3.91
3.91
3.91
3.91
3.91
3.91

.0
3.91
3.91
3.91
6.89
3.91
3.91
3.91
3.91
3.91
3.91
3.91

12
F

1.48
1.48
1.48
0.38
1.48
1.48
1.48
1.48
1.48
1.48
1.48


1.48
1.48
1.48
0.38
1.48
1.48
1,48
1.48
1,48
1.48
1.48

13
14
ULTROB ULTROE
BWEIR
0.00
0.00
0.04
0.04
0.04
0.04
4.38
4.40
4.35
4.22
4.09
3.91
BWEIR
0.00
0.00
0.00
0.00
0.00
0.00
0.44
0.39
0.26
0.11
0.04
0.01
= 0.50
0.00
0.00
0.04
0.04
0.04
0.04
4.36
4.35
4.22
4.09
3.91

= 0.50
0.00
0.00
0.00
0.00
0.00
0.00
0.38
0.26
0.11
0.04
0.01

15
YREACH

0.00
0.00
0.00
0.00
0.00
0.00
0.02
0.06
0.13
0.13
0.19
0.53

0.00
0.00
0.00
0.00
0.00
0.00
0.05
0.12
0.16
0.07
0.03
0.43
16
TIME
C
0.25
0.67
2.62
0.35
0.00
0.04
0.21
0.64
1.49
1.53
2.32

Q
0.25
0.67
2.62
0.35
0.00
0.04
0.21
0.64
1.49
1.53
2.32

17
TO TIME
= 4500
0.00
0.25
0.91
3.53
3.88
3.88
3.92
4.12
4.77
6.25
7.78
10.10
= 4500
0.00
0.25
0.91
3.53
3.88
3.88
3.92
4.12
4.77
6.25
7.78
10.10
NOTE:  DK and BWEIR correspond to Kj and b respectively in script.
                                                                                                                        o
                                                                                                                        CO

-------
110
The figures in column 8 of Table 3 show that the oxygen level increased by (12.09-11.50) = 0.59
ppm in just 5 miles of open water in reach 1, which is more than the cumulative first-order BOD in
all reaches.  In  the  same column, the results show that the amount of oxygen added through
aeration at the weir was approximately equal to the cumulative  first-order BOD of the wastes
added in all  reaches. It may be noted that more DO would  have been added in reach 1 and at the
weir if the deficit had been greater,

By consideration of the basic forces of oxygen supply and demand it was possible to write a series
of DO equations which satisfactorily represented the oxygen balance in the South Saskatchewan
River under  winter conditions.

It was found that the magnitude of  the first-order deoxygenation rate constant was not critical in
evaluating DO levels when the BOD5 of the waste water loadings @ 0°  C was known. The results
illustrated that  any opportunity for reaeration, as in  open water reaches and  at weirs, is very
beneficial in the oxygen economy of streams under winter, ice cover conditions.

                                  ACKNOWLEDGMENTS

The author  wishes  to acknowledge  that in writing this paper he has used a portion  of the work
reported  in his thesis which was supervised by Prof.  T. H.  Lackie  at  the  University  of
Saskatchewan,  Saskatoon, Canada, and supported financially by  the National Research Council
through Operating Grant A-3811.
                                      REFERENCES

 Anon (1964) Effect of Polluting Discharges on the Thames Estuary, Technical Paper No. 11, Her
     Majesty's Stationery Office, London.

 Bohnke,  B.  (1966)  New method of calculation for ascertaining  the oxygen  conditions  in
     waterways and the influence of the forces of natural purification. Adv. in Water Poll. Res.,
     Vol. l.p 157.

 Bouthillier, P. H. (1968)  Biological oxidation  in ice covered rivers, Proc. Third Canadian Symp.
     Water Poll. Res.,  Vol. 3, p 12.

 Cameron, R. D. (1967) Bio-oxidation rates under ice cover in the North Saskatchewan River, M.S.
     Thesis, Univ. Alberta, Edmonton, Alberta.

 Dobbins,  W. E. (1964) BOD and oxygen relationships in streams, J. Sanitary Engineering Div.,
     ASCE, Vol. 90, No. SA3. p 53.

 Gameson, A.  L. H.,  Vandyke,  K. G. and  Ogden, C. G. (1958) The effect of temperature on
     aeration at weirs. Water and Water Engineering, Vol. 62.

 Gameson, A.  L. H. and Wheatland, A. B.  (1958) The ultimate oxygen demand  and  course  of
     oxidation of sewage effluents, J. Proc. Inst. of Sewage Purification, Part 1, p 106.

-------
                                                                                 111
Gannon, J. J.  (1963)  River  BOD abnormalities. Department  of  Environmental Health,  Univ.
    Michigan, Ann Arbor.

Imhoff,  K., Muller,  W. J. and  Thistlethwayte,  D.  K.  B. (1956) Disposal of Sewage and Other
    Water-Borne Wastes, Butterworths Sci. Publ., London.

Lackie, T.  H. and Sparling, A. B. (1955) Sanitary survey of the Red River, Manitoba Dept. Health
    and Public Welfare, Winnipeg, Manitoba.

Landine, R. C.  (1962) Pollution in the South Saskatchewan River at Saskatoon, M.S. Thesis, Univ.
    Saskatchewan, Saskatoon, Saskatchewan.

Landine, R. C. (1970) Prediction of dissolved  oxygen levels in the  South Saskatchewan River,
    Ph.D. Thesis, Univ. Saskatchewan, Saskatoon, Saskatchewan.

Montgomery, H. A. C., Thorn, N. S. and Cockburn, A., Determination of dissolved oxygen by the
    Winkler Method and the solubility of oxygen  in pure water and sea water, J. Appl. Chem.,
    Vol. 14. p 280.

Owens, M., Edwards, R. W. and Gibbs, J. W. (1964) Some reaeration studies in  streams, Inter. J.
    Air Water Poll.,  Vol. 8, p 469.
Saskatchewan Research Council (1969) Physics Div. Saskatoon, Saskatchewan.
Saskatchewan Water Resources Commission, Poll. Control Br. Regina, Saskatchewan.

Saskatchewan Water   Resources  Commission  (1967)   Regina,  Saskatchewan, Water  quality
    management policy in the Province of Saskatchewan.

Schriek, W. (1963)   River  sedimentation  at  Saskatoon,  M.S.  Thesis,  Univ. Saskatchewan,
    Saskatoon, Saskatchewan.

Sparling, A. B. (1957)  Sanitary survey of the Assinibine  River, Manitoba Dept. Health and Public
    Welfare, Winnipeg, Manitoba.

Tywoniuk, N. (1969)  Unsteady flow  simulation of the South Saskatchewan  River, M.S. Thesis,
    Univ. Saskatchewan, Saskatoon.

-------
112
                                 APPENDIX I - NOTATION
 a
 b
 BOD
 BODS
 cfs
 DO
 DO

 fps
  FACT
  h
   2
  K2
  L
  mi
  mm
  ppm
  Q
  r
  ROD
  t
  V

  Y^EACH
                                                                       -1
coefficient in weir equation
coefficient in weir equation
biochemical oxygen demand
5-day biochemical oxygen demand
cubic feet per second
dissolved oxygen
DO deficit at beginning of reach, ppm
DO deficit at end of reach, ppm
feet per second
factor for converting BODS @ 20° C to BOD5 @ 0° C
mean depth of river, feet
fall height at weir, feet
first-order deoxygenation rate constant, to base e  day
first-order reaeration coefficient to base 10, day
first-order reaeration coefficient to base e, day
ultimate first stage BOD. ppm
mile
millimeter
parts per million
flow in cfs
deficit above weir/deficit below weir
residual oxygen demand, ppm per day
time, days
velocity in feet per second
BOD realized in time t
first-order oxygen demand exerted in reach due to waste water conditions

-------
       POLLUTION
A BIOLOGICAL STUDY  OF SOME  RECEIVING
     WATERS  IN  HOKKAIDO
                          Matsunae Tsuda, Toshiharu Watanabe
                                    and Kozo Tani
                                   INTRODUCTION

The (shikari River is about 365 km long and is the largest river in Hokkaido (Fig. 1). Its middle
and lower reaches  receive  wastes from manufacturing industries, a pulp mill, and coal mines.
Discoloration of the river water results  from the pulp mill and mine waste while the river bed  is
covered by the coal mine silt.
           IOOO
         «     tbetsu
         8     I96I f	
             1C
           FIGURE 1  Average water flow of the (shikari River at four stations
                              SOURCES OF POLLUTION
Upper Reach of the I shikari
Near the city  of Asahikawa  (pop.  245,000)  three  tributaries  - the Ushukubetsu  River, the
Chubetsu River and the Biei River - join the Ishikari River. The waste of the Kokusaku pulp mill is
discharged into the Ushukubetsu River and that of the Godo Alcohol Company factory into the
Chubetsu River. The effluent of the Kokusaku pulp mill has a BOD of 56.9 ppm and that of the
Godo Alcohol a BOD of 3,998 ppm in January 1959 (Kubo and Kosaka, 1960).
                                          113

-------
 114
                                         TABLE  1
                     Water Temperature, pH, Transparency of the Stations
                                 Studied in the Ishikari River
A  Sounkyo
B  Motoshirakawa
C  Furukawa
D  Kinseibashi
E  Shinbashi
F  Kyokuseibashi
G  Ushubetsu R., near Kokusaku
     Pulp Mill Effluent
H  Ushubetsu R., Midoribashi
I  Ino
J  Fukagawa
K  Sorachi R., Higashi-takegawa
L  Naie
M  Shimokawa
N  Ebetsu
O  Ishikari-ohashi
P  500 m downstream from
     paper mill effluent
Q  Toyohira R., Ganraibashi
R  Ishikari-cho
Water Temperature
       <°C)
       0.5
       2.8
       2.3
       2.8
       2.5
       6.5

       11.5
       11.5
       •0.5
        0
       1.0
       1.0

       1.0
       2.8

       7.0
       0.5
       1.0
PH
7.0
6.8
6.8
6.6
6.9
6.8

6.0
6.8
6.8
6.8
6.8
6.7

6.8
7.0

6.9
7.0
6.8
                                                                              Transparency
                                                                                  (cm)
46
12
45
18
25
11
11

 5
25

 6
30
 7
Middle Reach of the Ishikari
The  Sorachi and  the Yubari  rivers receive  coal  mine effluents. The  load  of the suspended
substances from the mines is estimated to be about 940 tons per day. Mine drainage and coal wash
waste contain very fine coal dust which changes the water  of the receiving river to a brown color
and covers its bottom with silt. The influence of the coal mine wastes to the river organisms is
physical - the deposited silt  makes it difficult for organisms to survive. It ruins fish spawning beds
and destroys flora and fauna. This form of pollution must  be considered apart from the ordinary
saprobic system classification.
Still another pollution source on the middle  reach  is an artificial fertilizer factory of the Toyo
Koatsu Company  located at Sunagawa. From this there  discharges effluent containing  much
inorganic substances especially SO4r the waste being heavily  toxic to fish.

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                                                                                     115
Organic Wastes Flowing in at the Lower Reach
A factory of the Kita-Nihon Paper Mill Company at Ebetsu discharges waste water of 45,000 tons
per day, its BOD being 176 ppm (Tamura, Fuji, Yuki, 1961). Sewage treatment effluent and other
sewage of the city of Sapporo (pop.  820,000), as well as industrial waste are discharged into a
tributary, theToyohira River.
 BIOLOGICAL  WATER QUALITY ASSESSMENT BY THE BOTTOM MICROORGANISMS

At 18 stations (from station A to station R) on the river, the microorganisms attached to stones,
support piling and other suitable substrate, were collected and studied at the laboratory.

Table 2 shows the organisms found at stations A through R.

Upper Reach

The upper reach of  the Ishikari was a clear mountain stream, with oligosaprobic waters, that were
rich in algae and benthic fauna.

     Station A (Sounkyo): A famous resort known for its hot springs.

     Station B (Motoshirakawa): A small tributary.

     Station C (Furukawa): 13 km downstream of Sounkyo.

At stations A, B  and C, transparency was  more than 45 cm. Many kinds of algae were found.
Effluents from the hot-bath resort at Sounkyo have no important effect upon the river water. The
benthic flora  consisted of blue-green algae, green algae and diatoms. A chrysomonad, Hydrurus
foetidus,  occurred at Station A and Bactrachospernum moniliforme at B; these species are both
cold-water kathorobic species. Among the diatoms, Ceratoneis arcus, Fragilaria capucina var.
lanceolata,  Gomphonema  oliuaceum   were dominant.  Stations  A,  B  and  C  were typical
oligosaprobic waters.

Asahikawa City and  Surrounding Area

Station E (Shinbashi): This station was located on the  left bank of  the Ishikari River several
hundred meters downward from the point where the Ushukubetsu River joins the main stream.
This  tributary receives waste of the Kokusaku Pulp Mill. Station E was heavily polluted and  had a
strong unpleasant odor. Here Chromatium colonies  cover the stones. There was Fusarium growth
which  occurs frequently  in waters  with strong organic pollution and the presence of  oxygen.
Scheuring and Zehender (1962)  write that Fusarium occurs more often in cellulose-containing
wastes  than the sewage bacteria Sphaerotilus. Practically no algae was found at this station. This
station belonged to polysaprobic waters.

Station F (Kyokuseibashi): This station was on the  right bank of the main stream, some hundreds
of meters  downstream  from  the junction of the tributary  Ushukubetsu  River, and 1 km
downstream from the pulp mill, on the opposite side of the stream from the waste effluent, thus

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 116
                                        TABLE 2

               Benthic Microorganisms Found at the Stations in the I shikari River

          SPECIES                                        STATION

                              ABCDEFGHI   J  KLMNOPQR

Bacteria
Zoogloea ramigera                                 +                          $     +
SphaerotUus natans                                       ********   +     t  +  +
Chromatium sp.                            t
Fungi
Alternaria sp.                                      *                    +
Fusariam sp.                                *             *
Blue-green algae
Chroococcus minutus          +                                                    t
Chlorogloea microcystoides                                                          *
Dermocarpa flahaultii                                                         *  +
Xenococcussp.                       +         +
Oscillatoria formosa                  ** + +   +
Oscillatoria sp.                                                                     +
Phormidium uncinatum                          $      t
Phormidium spp.              t                                    +
Lyngbya sp.                                                                  +
Homoeothrix janthina          *     ** +
Diatom
Melosira varians                   +     +     +      ++-f+4=      +  +  +      +
Cyclotella comta                                      +      +
Tabellaria fenestrata                +
Diatoma hiemale              +                                 +
Ceratoneis areas               #*»#^+     +         +         +
Fragilaria capucina             t   $  *                             +
   var. lanceolate
Asterionella formosa                                             +
Synedraulna                      $  +  +            ++  +   ++                   +
S. ulna var. Ramesi                   +  *     +         +  +                          +
S. capitellata f. striis                   +  +     +            +
Achnanthes linearis                +  +
A. Biasolettiana                   %
Cyrosigma acuminatum                                           +
Navicula mutica                                                 $
N. cryptocephala              *   +  +  +
N. exigua                             +
Cymbella ventricosa            +   +  +++
C. turgidula var. nipponica             +  +     +
C. tumida                               +
Gomphonema parvulum                          +
G. olivaceum                          $  +    **
Hantzschia amphioxys
Nitzschia linearis
N.palea                           4=

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                                                                                     117
                                    TABLE  2 (confd)


         SPECIES                                        STATION
                              ABCDEFGHI   J  KLMNOPQR
(keen algae
Ulothrix subtilissima                   +   *  T
U. zonata                      *   *  +   +  +                       +
Hormidium Klebsii                    +          +                   +                *
Geminella crenulatocollis                          +
Stigeoclonium lubricum                    *                          +
Rhizoclonium Hookeri              *
Blubochaete sp.                    £
Oedogonium sp.                    *
Closterium sp.                      +
Rhodophyceae
Batrachospermum moniliforme  *
Chrysophyceae
Hydrants foetidus              *
Ciliata
Vorticella campanula                                                                     +
Carchesium polypinum                                         *                          *
Carchesium sp.                                                                  +


              ** very rich,   *  rich,   *  common,   +  rare,   +  very rare
unaffected. Many kinds of blue-green algae, green algae and diatoms were found. This station was
oligosaprobic.

Station G (Ushubetsu River, Kokusaku Pulp): This was  near the out-fall of the waste from  the
Kokusaku Pulp Mill on the right bank of the Ushukubetsu River. There was an unpleasant odor of
factory waste which included the smell of hydrogen sulphide. The river water was dark brown in
color. Stones were black-colored on their bottom surfaces due to sulphides. There were no aquatic
insects. Growth on the stones consisted of Zooglea andAItemariasp. (fungus), both of which are
polysaprobic species which live  in slow-running  streams. This station belonged to polysaprobic
waters.

Station H (Ushubetsu River, Midoribashi): This was also a station of the Ushukubetsu River, 1  km
downstream from the paper mill. It was situated on the opposite side of the factory, but evidently
influenced by the factory waste, as indicated by  blackening of the bottom surfaces of the stones.
Attached algae consist of blue-green algae (Phormidium uncinatum) and diatoms.

Station  I  (tno)  and Station J  (Fukagawa):  Both stations were on the left bank of the river.
Influence of the paper mill was stronger here than on the other bank. At both stations there was
an odor of pulp waste, brown water with reduced transparency, and the bottom surfaces of stones
blackened. Sphaerotilus and Fusarium were found concurrently with diatoms. Both stations were
a-mesosaprobic* (am+ means the  class belonging to  am, but more strongly polluted than  the
average am).

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 118
The Sorachi River and Sunagawa

In this reach the Ishikari River received the effluents of many coal mines. The wastes contained
almost no organic compounds. Their effect on the river organisms was mostly the physical effect
of siltation.

Station K (Higashi-takigawa): This station is at the Sorachi River, a tributary. Due to the coal mine
waste, the water was brown-colored, with low transparency. The river bed was covered by silt and
coal dust. Organisms were very scarce. Study of algae attached to stones covered by silt revealed
that the flora consisted only of diatoms. (Table 2).

Station  L (Naie): Located on the left bank of the main stream, this was 20 km downstream from
the junction of  the Sorachi River and 5  km downstream from the out-fall of the waste of the
Toyo-Koatsu factory. Transparency was reduced and the water was brown in color.

Lower Reach and the Toyohira River

Station  M (Shimokawa): This station was 40 km downstream from Station  L. At  both Station L
and M, a few blue-green algae and diatoms were found. Sphaerotilus and fungus were also present,
but in small quantity. Both stations are a-mesosaprobic.

Station  N (Ebetsu): This station was 1 km downstream  from the junction of the Yubari River,
which carries a  large amount of silt from coal mines  into the Ishikari River. The river bed was
covered by silt. Only two species of diatoms were represented here, and no benthic animals were
found.

Station O (Ishikari-ohashi): This station was 1.5  km downstream from the junction of the  Ebetsu
River. There was  much silt on the river bed, however  transparency was  recovered (Table  1).
Micro-flora on stones consist of  Zooglea. Sphaerotilus,  blue-green algae and  diatoms. The  station
was cc-mesosaprobic+.

Station P: About 500 m downstream from the waste of the Kita-Nihon Paper Mill factory and also
the  out-fall  of cooling water  of  a heat-engine plant;  its water was  brown-colored, with  an
unpleasant  odor. Sphaerotilus,  blue-green  algae  and diatoms were  sparse. The station was
polysaprobic.

Station Q (Ganraibashi): This station was on the Toyohira River, a tributary which flows through
Sapporo City, the  largest city in Hokkaido. The  station was about 300  m downstream from the
night soil treatment  plant. Algae  on  stones consist mainly of blue-green  algae,  Hormidiun  sp.
(green algae), Zooglea and Sphaerotilus occurred too.

Station R  (Ishikari-cho): This station  was  at Ishikari-cho, a town 5 km downstream  from the
mouth of the river. Water was  brown in color, with transparency of 7 cm. Ciliates and a few
diatoms  were found. The diatoms  consisted of such  species as Synedra ulna, Nitzschia palea,
Melosira variens, and Navicula cryptocephala. The  station was a-mesosaprobic*.

Figure 2 shows the water quality  map  made on the  basis  of the biological assessment  by the
above-mentioned data on microorganisms.

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                                                                                      119
                                                              50 —
                                                              100 —
                                                              150-
                                                             200 —
                                                             230 -
          FIGURE 2  Water quality map of the Ishikari River by biological assessment
                                   BENTHIC ANIMALS

Tables 3 and 4 show the benthic animals found at Stations A through R.

Upper Reach

The upper reach of the Ishikari was rich in benthic fauna.

Station A (Sounkyo): Large numbers of benthic  species were found; the water was clear. The
net-spinners coefficient (this equals the  ratio of the biomass by weight of net-spinning caddis fly
larva to the biomass of total benthic  animals) was 82%, showing that the community  was stable,
i.e., at climax or near climax. Station A was oligosaprobic.
Station B (Motoshirakawa): Similar to Station A, oligosaprobic.

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  120


                                        TABLE 3

                 Benthic Animals Found in Three Stations in the Upper Reach
                                   of the (shikari River

          SPECIES                                        STATION

                                      Sounkyo          Motoshirakawa         Furukawa
                                          ABC

 Ephemeroptera
 Paraleptophelebia sp.                       +                                        +
 Ephemerella basalis
 Ephemerella ru fa
 Ephemerella nigra                          +                                        +
 Ephemerella sp. nay                        £
 Ephemerella sp. EC                        ±                   $
 Ephemerella sp. ER                                                                 ±
 Baetis sp.                                 +
 Baetiella sp.                                                                        +
 Isonychia japonica                         +
 Epeorus uenoi                             +
 Epeorus latifolium                         +
 Rhithrogena sp.                            +
 Cinygma sp.                               +                                        $
 Plecoptera
 Nemoura sp.                               *                   +
 Amphinemoura sp.                         *                                        t
 Protonemura sp.                            £                                        t
 Capnia sp.                                 +
 Megarcys ochracea                         +
 Isoperla towadensis                        $                                        $
 Hemiptera
 Notonecta trigutta                                             +
 Sigara nigroventralis                                                                 +
 Neuroptera
 Stalls sp.                                                      +
 Trichoptera
 Rhyacophila articulata                      +
 Rhyacophila brevicephala                                                            +
 Rhyacophila sp. RG                        £                                        £
 Mystrophora sp. (Larva)                    +                                        *
 Mystrophora sp. (Pupa)                     *                                        i
 Stenopsyche griseipennis                    *                   •»•                    i
 Arctopsyche sp. E                        +                                        +
 Hydropsyche ulmeri                        *                                        ^
 Hydropsyche sp. HB                                                                 +
 Molanna falcata                           +                   +
 Neophylax ussuriensis                      t
 Glyphotaelius admorsus                                        +
 Stenophylax sp.                                                +
 Goera japonica                                                t                    +
 Brachycentrus sp.                          ^
 Micrasema sp.                                                                      4-
 Coleoptera
Philorus ezoensis                           +
 Tipula sp.                                                     +                    +
Antocha sp.                               i                                        ^
Spaniotoma sp.                            *                                        $
Atherix sp.                                +                                        +
Turbellaria
Dendrocoelopsis sp.

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                                                                                      121
          SPECIES
           TABLE  4

Benthic Animals of Stations E - R

                             STATION
Ephemeroptera
Ephemerella sp. EC
konichia japonica Ulmey
Plecoptera
Isoperla towadesis Okamolo
Trichoptera
Neoseverinia crassicornis Ulmey
Coleoptera
ttybius apicalis Sharp, adult
Dipt era
Tipula sp.
Antocha sp.
Spaniotoma sp.
Tendipes sp.
Crustaceae
Gammarus nipponensis Veno
Asellus ripponensis Nichols
Oligochaeta
Tubifex sp.
Hirudinea
Mimobdella sp.
                                           H
                  I
   rich,
K
M   O   P    Q   R
                                           common,   +  rare
Station C (Furukawa): Similar to Station A, oligosaprobic.

Asahikawa City and its Neighborhood

Station  D (Kinseibashi): The  water was  clear; transparency was 46 cm. There were very few
animals  due to the devastation of the bottom by gravel-dredging. Kubo et al. (1961), at this
location recorded larvae of some species of mayflies, stoneflies and caddisflies.

Station E (Shinbashi): This reach was extremely polluted by the waste of the Kokusaku Pulp Mill.
Mimobdella sp. was the only animal found here. Station E was polysaprobic.

Station  F (Kyokuseibashi):  Some hundreds  of meters downstream from  the junction of the
Ushukubetsu River, it was on the other side of the pulp mill, so there was little influence from the
waste. Ephemerella sp. EC and Isoperla towadensis, which are clear-water species, were collected
here. This station was oligosaprobic.
Station G (Ushubetsu River): This was located at the out-fall of the waste of the Kokusaku Pulp
Mill. No bent hie animals.

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122
Station H (Ushubetsu River, Midoribashi): Station H was located 1 km downstream from the mill.
Tendipes sp., Asellus sp., and Tubifex sp. were found, all of which are pollution-tolerant species.
This station was0-mesosaprobic~.

Station I (Ino): Tendipes, Tipula, Asellus, Mimobdella, and Tubifex were found. The station was
a-mesosaprobic*.

Station J (Fukagawa): Tendipes, Asellus, and Mimobdella were found. Besides clean-water insect
species such as Ephemerella sp. EC, Neoseverinia crassicornis were found.

Lower Reach

Due to inflow of silt from the Sorachi River, a tributary, the river bed was covered by silt and coal
dust. Almost no stones were found.

Station K (Higashi-takigawa): Station K was  represented by Tendipes and Tubifex.

Station  L (Naie>: At Station  L Isonychia japonica, Gammarus, Asellus, Mimobdella and Tubifex
were found. Station L was /3-mesosaprobic".

Station M (Shimokawa): The  bottom at Station M was covered by silt and Ilybius apicalis was
present.

Station N (Ebetsu): Silt and coal dust from coal mines characterized Station N; no benthic animals
were found.

Station 0 (Ishikari-Ohashi): Gammarus sp. was found at Station O.

Station P: Station P was  located 500 m downstream from the paper mill. The water was brown,
and Tubifex and Entosphenus japonicus sp. were found. Lamprey were widely distributed in the
middle and lower reaches of this river. They were found even in polluted waters, and seemed to be
very tolerant of the pollution.

Station   Q (Ganraibashi): Located on the Toyohira River  downstream  from Sapporo.  The
transparency of the water was 3 cm. Tendipes, Asellus, Tubifex and Entosphenus japonicus were
found; Tubifex was very abundant. Station Q was a-mesosaprobic.

Station  R (Ishikari-cho): The water transparency was 7 cm. The water color was brown and the
bottom was covered with mud. Tubifex was present. Station R was a-mesosaprobic*.
                                      DISCUSSION

 When we assess water quality biologically, we must consider two kinds of effects separately:

     (a)  The effect of organic pollution from municipal sewage and paper or pulp mills.

     (b)  The effect of silt from coal mines.

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                                                                                      123


The normal saprobic system analysis  can be used for  (a) but not for (b). The  effect of silt  is
recognized only by the following: when the effect is large, only few (or even no) species and only
a few individuals  will be found  on the bottom of the river, and when the effect is small, more
species and more individuals will  be found. But in the case of organic pollution, we have indicators
for every class of water quality.

In this river, the pollution by  the pulp mills  (and paper mill) is  the  most serious problem,
especially the pollution by the factory  of the Kokusaku Pulp Mill Company in Asahikawa City.

At Sunagawa. 90 km downstream from the factory the water color and  BOD of the river water
have recovered, but COD value is still  high (40 ppm), and almost the same value continues to the
estuary (Nakamura, 1961).

The importance of the dissolved  organic materials  from the peat zone  in the drainage basin of the
I shikari  should be  also considered.  These dissolved peat-originated substances are  like the
substances from the pulp wastes  (lignin, cellulose,  etc.) -  very hard for bacteria to decompose. It
must also be considered that the water temperature is low in most months of the year in this part
of Japan. These are the  reasons why the brown water color and high COD value hold in the whole
middle and lower courses of the Ishikari River.

Suspended solids such as silt and sand  from the coal mines are deposited on the bed of the Ishikari
River, to which they are  carried by  the tributaries.  The  silt and sand will be carried farther
downstream rolling on the  bed. The bottom substances do not rest, since the bottom is not stable,
thus the development of the benthic  microorganisms, including bacteria,  is very  poor, indicating
the  reduced potentiality of natural purification of this river.

For the past two  or three years  the situation has improved. Many coal mines have stopped their
operations owing to the increased cost-gain relationship. The pulp mill in Asahigawa City is moving
part of its machinery to its other  factory located nearer the sea.
                                       REFERENCES

 Kubo, T.  and Kosaka, J. (1960) Influence of industrial wastes discharged to the Ishikari  River
     (between Asahigawa and Takigawa) on the distribution of organisms, Suisan-zooshoku-shiryo,
     P. 1-

 Kubo, T., Kosaka, J., Inoue, S.. Ito, T. and Yoshizumi, K. (1961) Influence of industrial wastes
     discharged  to  the  middle reach of the  Ishikari  River  on the distribution of the aquatic
     organisms, Suisan-zooshoku-shiryo, p. 1.

 Nakamura,  T.  (1960)   Studies  on  River Pollution:  I.  Studies  on  the water  quality and
     contamination of the Ishikari River, Report of the Hokkaido Institute of the Public Health,
     No. 6.

 Scheuring,  L. and Zehender,  C.  (1961)  Untersuchungen  zur  Stoffwechselphysiologie des
     "Abwasserpilzes" Fusarium aquaeductum, Lagh. Schwez., Z. Hydrol., 24, 158.

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 124


Tamura, T., Fuji, A. and Yuki R. (1961) Influence of industrial wastes discharged to the middle
     reach  (between Takigawa and  Ebetsu) of  the  Ishikari  River  on the aquatic organisms,
     Suisan-zooshoku-shiryo, p. 1.

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            CHEMICAL  EFFECTS  OF  SALMON  DECOMPOSITION
                           ON  AQUATIC  ECOSYSTEMS
                           David C. Brickell and John J. Goering
                                    INTRODUCTION

The Pacific salmon (Oncorhynchus sp.) is a valuable source of food energy from the sea and its
potential is not yet fully realized. The two most highly evolved species of the genus, O. gorbuscha
and O. keta, are true marvels of efficiency from the anthropomorphic vista. Upon hatching in the
gravels of  coastal streams and rivers each  spring, the salmon fry  of these two species migrate
immediately to the sea to harvest the productivity of the ocean waters. Their migrations extend
over vast areas of  the Central North Pacific.

After one year of residence in the ocean these salmon are compelled by instinct to return to their
natal waters. This homeward migration results in  the transfer of millions of pounds of organic
matter, once widely distributed in  the  open ocean, to  the coastal waters where salmon spawn.
Thus, the vast primary productivity of the open ocean, which is currently  too diffuse to harvest
economically, is brought within man's grasp. This directed biomass transfer is sufficiently large to
be considered a "biological current" originating in the Central North Pacific and terminating in the
freshwater  streams of the coast.

In addition to the large commercial harvest, of which a portion, about 20% by weight, is returned
to the ocean as waste from processing  plants, millions more salmon enter  freshwater streams to
spawn and  inevitably to die and decompose. The fate and distribution of this organic matter has
previously received little attention.

Although  the  decomposition  of  salmon  carcasses  in the  marine environment  is  a  natural
phenomenon, the possibility that localized accumulations of seafood waste products, as might
occur in  the vicinity of processing plants, may stress the marine environment beyond its capacity
to maintain stability must be considered.

Our interest in the fate of organic matter associated with seafood processing waste was stimulated
by a Bering Sea cruise of the R/V ACONA, cruise number 066, in June 1968. In samples taken off
the coast of Alaska in areas of significant seafood processing, namely in the area of Kodiak, Alaska
and Unalaska, Alaska, we observed a water layer with extraordinarily high concentrations of
ammonium. Near the processing plants toxic ammonium concentrations approaching 25 Mg-atom
NH^-N/liter were  observed while lower yet distinctly elevated concentrations were observed over
tens of square miles of ocean in the area.

Other cruises of the R/V ACONA in the fjords of Southeast Alaska have revealed moderately high
concentrations  of ammonium  at  about 20-30 m.  Evidence  suggests that the origin of this
ammonium is within the estuary rather than from  the sea. Since the streams of Southeastern

Alaska are  abundant with salmon, the observed concentrations of ammonium may represent the
results of carcass decomposition within the estuary.

                                          125

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 126


 To increase our knowledge of the biological and chemical effects of the decomposition of seafood
 material, we have initiated a study of the decomposition of salmon carcasses in a natural system in
 southeastern Alaska (i.e. Little  Port Walter estuary). The  Pacific salmon migrates through this
 estuary when  returning to  its natal stream to  spawn.  Following spawning, the fish "die and the
 carcasses are eventually carried to the estuary where they sink to the bottom. During periods  of
 low stream  flow, the dead carcasses may remain in the stream itself  until higher stream flows
 transport them to the estuary. In years of large escapements, the density of fish in the spawning
 stream can  be very high. In the  system chosen  for our work, spawning densities greater than six
 fish  per m2 have  been recorded, although  at the  time  the  current  study was conducted the
 spawning density was slightly more than two fish per m2. Since our system involves primarily pink
 salmon (O. gorbuscha). the average weight of the fish can be assumed to  be 2-3 kilograms.

 Thus, our study is  concerned with the fate  and distribution of some  75 metric tons of organic
 matter in  the form of salmon  carcasses in  one small estuary in Southeastern Alaska. We are
 particularly  interested in determining: (1) the effects of the salmon carcass decomposition on the
 nitrogen chemistry of the water  in which the decomposition occurs; (2) the  form and distribution
 of  the organic  matter which is  returned  to  the  marine system; and (3) the rate at which
 remineralization occurs. This paper presents the results of our initial investigations.

                                        METHODS

The system selected for study included  a pink salmon spawning  stream, Sashin Creek, and  its
associated estuary.  Little  Port Walter,  on Baranof  Island, Southeastern Alaska. Another  small
estuary in the vicinity, Toledo Harbor, was used as a control for the estuarine studies as it did not
 support a salmon run.

Sashin Creek flows some 3,000  m from Sashin Lake  to the Little Port Walter estuary. A high
waterfall prevents further upstream migration of the salmon, and hence spawning is limited to the
 lower 1,200 m. The stream area  above the water fall was used as a control  for the stream studies
since this area revealed seasonal variations in water chemistry but was not influenced by salmon. A
 permanent weir for counting fish entering the stream is located at high tide level.

The U.S. Bureau of Commercial Fisheries has maintained a research station at Little Port Walter
 since 1934  for the purpose of collecting information on the freshwater ecology of pink salmon.
 These studies have resulted in the definition of  3 distinct ecological areas of the  stream: an upper,
 middle and  lower area. To maintain  integrity with existing data, we observed the same sampling
 boundaries  in the  stream. The total area of Sashin Creek available for  spawning is about 13,600
 m2. The width of the stream varies between 12 and 24 m. Stream discharge data for Sashin Creek
 has been collected since 1951 and ranges from 8.0 to 700 cubic feet per second with a mean of 80
 c.f.s.

The Little  Port Walter  estuary is small, consisting of an inner and outer bay with a constriction
 between the two. The distance from the mouth of Sashin Creek at high  tide  to the entrance to the
outer bay is approximately 1.5  km, and the maximum width is about 0.4 km.  The maximum
depth at low tide is 44  m for the outer bay and 21 m for the inner bay. The  connecting channel is
 27 m wide and about 6 m deep at low tide. Tidal variations range to 4.6 m. A detailed description
of the oceanography of Little Port Walter estuary is given by Powers (1962).

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                                                                                      127
Toledo Harbor, about 3 km south of Little Port Walter, has dimensions approximately the same as
the inner bay of Little Port Walter. The freshwater stream entering the harbor has a waterfall just
above high tide  level and does not therefore support a salmon run.

Stream Studies

Prior  to the arrival of the salmon, surface water samples were  collected  weekly in Sashin Creek
above the waterfall and at the lower end of each of the three designated ecological areas  of the
stream. Analyses for NO:-N,  NOj-N, NH4*-N, dissolved organic -N and  inorganic phosphate were
performed. Nitrite was determined by the Griess method as applied to seawater by Strickland and
Parsons (1965). Nitrate was determined by conversion  to nitrite in a cadmium-mercury reduction
column based  on  a method by  Grasshoff  (1964)  and  determined  as nitrite. Ammonium was
measured using the recent method of Solorzano (1969). This method is  specific for ammonium
and does not measure labile  amino  nitrogen.  The ammonium method of Richards and Kletsch
(1964) was  used  to  obtain  the Bering Sea ammonium  values. This method is not specific  for
ammonium -N  but measures  a considerable fraction of labile amino  nitrogen as well. Dissolved
organic nitrogen was  determined by converting it to nitrate by ultraviolet light oxidation in  the
presence  of  oxygen according to the method outlined by  Armstrong, et al  (1966). Reactive
phosphorus was determined by the method of Murphy and Riley (1962). Samples were collected
weekly beginning in August and continuing into November, about 2 months beyond spawning.
                   53'55'
                              O STATION LOCATIONS
                                IN DUTCH  HARBOR
                              * SEAFOOD  PROCESSING
                                SITES
BERING
  SEA
                          APPARENT
                          TIDAL CURRENT
                          DIRECTION
                                                     UN4LASKA  ISLAND
                         •J CAPTAINS  O
                             BAY
                          166*35'                      I66'30'

                       FIGURE 1   Iliuliuk Bay, Unalaska Island, Alaska

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128
                                       TABLE 1

     Chemical and Physical Characteristics of Water in Iliuliuk Bay at Stations 2327
              Near Seafood Processing Sites and at Station 2351 further Seaward
2349
  Station
Number and Depth in Temp.
Location Meters C
2349
53°51.8!N
166 33.3 W




2347
53°52.8*N
166 32.7 W
2341
53°52.8'N
166 31.5 W


2337
53°53.2*N
166 31.1 W


2331
53°53.?!N
166 30.6 W


2327
53°54.2jN
166 30.2W

2351
54°01.3!N
166 04.5 W



0
5
10
15
20
30
40
0
5
10
0
5
10
15
25
0
5
10
15
25
0
5
10
15
25
0
5
10
15
0
5
10
20
30
50
5.70
5.63
5.01
4.81
4.34
3.70
3.30
7.35
5.52
5.20
6.71
5.98
5.39
5.03
3.83
5.95
5.86
5.47
5.19
3.79
6.70
5.87
4.92
4.64
4.11
6.02
5.68
5.22
-
4.87
4.88
4.88
4.87
4.88
4.87
. Salinity
o loo
32.051
32.005
32.237
32.266
32.294
32.360
32.343
24.906
32.171
32.223
30.782
31.667
32.202
32.366
32.373
31.788
31.820
32.265
32.313
32.381
30.781
32.109
32.304
32.347
32.362
31.777
32.146
32.376
32.391
-
32.431
32.408
32.502
32.412
32.523
Oxygen PO;3-P NH4+-N
ppm Mg-atomAiter
7.91
7.97
7.67
6.90
7.14
6.84
5.60
6.78
7.17
7.39
7.98
8.05
7.82
7.35
4.30
8.07
8.08
8.10
7.83
4.84
7.88
8.34
7.51
7.36
5.51
7.93
7.97
7.59
7.28
-
-
-
-
-
1.08
1.10
1.35
1.44
1.69
2.12
2.45
1.22
1.78
1.50
0.51
0.87
1.21
1.47
5.03
0.84
0.88
0.98
1.20
4.43
0.48
0.83
1.42
1.80
3.37
0.70
0.96
1.13
1.42
1.30
1.29
1.25
1.26
1.25
1.26
0.4
0.4
0.8
0.8
1.0
0.9
1.0
5.2
8.1
5.7
1.8
3.4
4.6
5.9
23.8
2.4
2.3
2.2
4.9
19.9
1.7
2.0
6.4
9.3
18.4
2.7
3.2
5.0
6.5
3.4
3.6
3.2
3.3
3.2
3.2
NO2~-N
/ug-atom/liter
0.17
0.16
0.19
0.19
0.20
0.20
0.22
0.19
0.26
0.23
0.06
0.11
0.15
0.16
0.33
0.12
0.14
0.12
0.15
0.33
0.06
0.12
0.17
0.21
0.28
0.09
0.10
0.13
0.16
0.16
0.17
0.18
0.17
0.17
0.17
NO3"-N
Mg-atom/liter
5.8
6.0
7.8
11.2
13.1
18.3
20.9
0.9
5.1
6.6
0.2
2.2
4.7
6.4
9.2
3.0
3.0
4.5
5.6
9.6
0.5
3.4
6.7
7.7
9.9
2.3
3.2
5.7
7.0
12.0
11.7
11.5
11.8
11.8
12.3

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                                                                                      129
Estuary Studies

In the  estuary, weekly samples were collected at selected depths in both Little Port Walter and
Toledo Harbor. The same chemical  analyses and procedures were employed as were used in the
stream  studies.
                                         RESULTS
Iliuliuk Bay and Bering Sea Studies
The  locations of sampling stations  and seafood  processing plants  on Amaknak and Unalaska
Islands,  which are located  near  Unimak Pass  in the Aleutian chain, are  shown in Figure 1. The
oceanographic parameters observed in the area on cruise 066 indicated that during our sampling
period in June 1968 the tidal current entered  the  area from the northwest and exited toward the
northeast. The temperature-salinity-oxygen characteristics in the Captain's Bay area where station
2349 is  located suggested an open ocean environment little affected by the waste of the processing
plants,  while those stations to  the  northeast of  the processing plants  revealed rather marked
chemical alteration. Table 1 presents the chemical and physical parameters obtained at all stations.
Station 2349, indicative of the water entering the  area of seafood processing, had a normal open
ocean ammonium concentration  of approximately  1/ug-atom NH^-N/liter at 25 m while the
ammonium concentration  at 25 m  at station 2341 was 23.8jug-atom NH^-N/liter,  which is an
extraordinarily  high concentration for sea water. Station  2351, further seaward, exhibited the
chemical characteristics which result after the  water from Iliuliuk Bay has mixed with Bering Sea
water. The ammonium values  obtained in this study of Iliuliuk Bay were determined using the
method  of Richards and Kletsch (1964). This method does not distinguish ammonium -N from
labile amino -N. Because  of the highly organic nature of the seafood waste a considerable fraction
of the nitrogen reported here as ammonium -N  could be amino -N.

Figure 2 presents a plot of the ammonium and  oxygen concentrations  with depths at stations
sampled in Iliuliuk Bay. The results show a drastic  increase in the ammonium concentration of the
                    »2J49
                                                               2349
                                   jj g-dtoms N*C-N/liter
FIGURE 2  NH4-N and oxygen at various stations and depths in Captain's Bay and Iliuliuk Bay

-------
 130


waters while in residence in tliuliuk Bay. Whereas that water entering the bay from Captains Bay
has an ammonium concentration  of approximately 1/ig-atom NH^-N/liter. The concentration of
ammonium in the bottom waters within the bay increases to almost 25/ug-atom  NH^-N/liter.
Likewise,  the  oxygen  concentration  of  the  bottom  waters  is  lowered.  The  ammonium
concentrations are high at intermediate depths, 5 - 10/wj-atom NH^-N/liter at 15 m, but the most
significant increase in ammonium  and decrease in oxygen  occurs between 15 and 25 m. Since the
25 m sample is near the bottom, the substantial increase in ammonium at this depth probably
results from decomposition of organic matter which has accumulated on the bottom.

The data for  station 2351 indicated a well mixed water column with the ammonium distributed
rather  uniformly  through the column  from  the surface to 50 meters. Other seaward stations
displayed  decreasing  but  elevated ammonium  concentrations,  suggesting   that  ammonium
originating in  Iliuliuk Bay has an influence on the nitrogen economy of the surrounding ocean.

Stream Studies

After evaluating the data from the Iliuliuk Bay  and Bering Sea study we decided to examine a
natural  phenomenon  which  results in  the accumulation  of organic matter  in  the  marine
environment similar to the situation observed in  the vicinity of seafood processing sites. Salmon
inevitably die following spawning. This results in the accumulation  of salmon carcasses both in the
freshwater stream where spawning occurs and in the  receiving estuary. This natural system was
selected for study because it represented  a cyclic  phenomenon which could  be  followed from
beginning to end with little external influence.

About 30,000 pink salmon spawned in  the 1200 m of Sashin Creek in 1969. After spawning and
death many of these  carcasses remained in the stream for a period of time before being washed
into the estuary. Some of these were scavenged,  but the majority  of the carcasses were deposited
on  the  bottom of tine Little  Port Walter  estuary.  In following the chemistry  of salmon carcass
decomposition we were particularly interested in the nitrogen chemistry. Since fish flesh contains
much protein we felt  that the various forms of nitrogen would be  excellent indices of the rates of
biological decomposition of salmon carcasses.

Surface water samples were collected and  analyzed weekly from four different sites in the stream;
above the waterfall which prevented further upstream migration of the spawners. Area O, and at
the  lower  boundary  of each of  the  three  defined ecological areas. These boundaries were as
follows: Area I, waterfall - 430 m downstream; Area II. 430 - 730 m downstream; and Area  III,
 700 - 1200 m downstream. The  first 300 m of stream below the waterfall  is not favorable  for
 spawning and hence only a few carcasses are deposited here.

Since  the  water  at each  sampling area  downstream  had been exposed to more  carcasses, we
expected a systematic increase  in the  concentrations  of  metabolites resulting  from carcass
 decomposition as we moved progressively downstream.

 Water samples collected prior to entrance of the fish into  the stream showed little variationjn
 water chemistry  from above the falls  to  the mouth of the stream. On August  31, the NH4-N
 concentration above the fall was 0.32 /Ltg-atom N/liter while at the stream mouth the concentration
 was 0.46 Mg-atom N/liter. Similarly, the dissolved  organic nitrogen concentration above the falls on
 that date was 3.3 MQ-atom N/liter, while at the stream mouth an organic nitrogen concentration of
 3.8 Mg-atom N/liter was observed.

-------
                                                                                       131
 Spawning activity commenced in  late August and  by early September dead carcasses began to
 appear in the stream. The first noticeable chemical  effects of decomposition were observed in the
 stream on September  14. On this date, the ammonium concentration above the falls was 0.40
 jug-atom  N/liter while at 1200 m downstream the concentration increased to  1.73 jug-atom N/liter.
 Likewise the dissolved organic nitrogen concentration increased from 4.0 jug-atom N/liter to 7.4
 jug-atom  N/liter during the traverse. As the number of carcasses increased, the downstream increase
 in ammonium  nitrogen  and dissolved  organic nitrogen became greater. On September  29 we
 observed the greatest difference in stream chemistry  between the control area and the lower end of
 the stream. The ammonium concentration  increased from 1.66 jug-atom N/liter above the falls to
 7.80 /ug-atom N/liter  at 1200 m downstream.  Dissolved  organic  nitrogen  increased from 5.7
 /;g-atom  N/liter to 17.7 jug-atom N/liter. The concentration  of NH4+-N and dissolved organic -N
 observed at each sampling site and date are presented in Table 2 and in Figures 3 and 4.
                                        TABLE  2

           The Concentrations of Ammonium -N and Dissolved Organic -N (D.O.N.)
                       Observed in each Sampling Area of Sashin Creek

                       Concentrations are Expressed as jug-atom-N/liter
A AreaO
Date
8/24/69
8/31/69
9/7/69
9/14/69
9/22/69
9/29/69
10/8/69
10/16/69
10/28/69
NH4-N
0.20
0.32
0.32
0.40
1.31
1.66
1.56
1.44
1.63
DON
3.04
3.29
3.38
4.04
5.83
5.71
5.23
5.22
4.84
Area I
NH4-N
0.60
0.38
0.64
0.33
1.44
4.59
4.48
4.04
2.46
DON
3.18
3.39
3.64
5.31
6.44
7.38
6.72
6.11
6.02
Area II
NH4-N
0.62
0.38
0.92
1.40
3.22
6.55
6.62
6.72
3.88
DON
3.27
3.49
4.84
6.10
8.22
12.40
10.52
8.43
7.02
Area
jT
NH4-N
0.68
0.46
0.98
1.73
4.17
7.80
7.66
7.02
5.63
III
DON
3.67
3.84
5.39
7.36
9.71
17.67
16.8
10.32
8.64
Estuary Studies

Water samples in the Little Port Walter estuary and in the control estuary, Toledo Harbor, were
collected weekly at 1, 4, 8 and 12 m. Dissolved organic nitrogen proved to be the most valuable
index of  the salmon   carcass decomposition phenomenon. The dissolved  organic  nitrogen
concentrations observed  in  Little  Port Walter and Toledo Harbor appear  in Table 3. Figure 5
compares graphically the dissolved organic nitrogen of the surface waters of  the two estuaries.
Figure 6 is a comparison of their organic nitrogen concentrations at 12m.

The first effects of salmon carcass decomposition on the water  in Little Port  Walter estuary, as
evidenced by  increases  in dissolved organic nitrogen, were not observed until about 15 days after

-------
  132
          8/24    8/31     9/7     9/W    9/22    9/29    IO/8    10/16    10/28

                                           DATE

             FIGURE 3  Concentrations of NHVN in Sashin Creek surface water
3/16/7O
increases were first observed in the stream. Heavy rains in late September resulted in flushing most
of the carcasses from the stream  into the estuary where they sank to the bottom. The dissolved
organic nitrogen concentration in the surface water of Little Port Walter estuary began to increase
on September 22  and reached  a  peak of 103 jug-atom N/liter on October 28 (Fig. 5} while the
surface concentration  in  Toledo Harbor remained almost steady at about 5.4 pig-atom N/liter
throughout this period.
The data on ammonium concentrations for the two estuaries did not reflect the immediate effect
of carcass decomposition. The concentrations  in  fact declined during the fall months from a
summer high. The ammonium concentrations observed at 12 m depth in  the  two estuaries are
presented in Figure 7.

-------
                                                                                 133.
8/24
8/3!
9/7
9/14
1/8
                                                           10/16
                               9/22     9/29




                              DATE



FIGURE 4  Concentrations of dissolved organic -IM in Sashin Creek surface water

-------
 134
                                        TABLE 3

           Dissolved Organic Nitrogen Concentrations Observed in Little Port Walter
                  and Toledo Harbor Estuaries in Summer and Fall of 1969
                         Concentrations Expressed asjug-atom-N/liter
Little Port Walter
Depth 8/24
m
1 2.42
4 2.64
8 2.42
12 2.56
Toledo Harbor
1 2.07
4 1.87
8 3.21
12 2.46
10 -
8/31 9/7 9/14 9/22
2.40 3.96 3.27 3.78
1.46 3.03 3.40 1.48
1.32 3.02 3.18 1.09
3.90 3.38 3.65 1.80

1.52 1.45 1.34 1.23
0.65 1.69 1.41 1.20
1.60 1.98 1.88 1.32
3.09 2.14 2.35 1.92

9/29 10/8 10/16 10/28
5.46 6.62 9.20 10.33
3.36 7.52 4.86 10.83
3.50 2.55 11.61 9.11
6.53 8.92 16.26 14.26

5.24 5.48 5.42 5.32
5.60 5.66 5.63 4.27
4.98 3.45 4.99 5.39
4.93 4.63 5.02 5.42
1 1 1
_/"\
11/14
5.62
4.83
7.68
12.43

5.02
4.22
4.87
5.20
_
J? LITTLE PORT WALTER / \
'— g . surface — >. / \
ai
o
-0 6 -
5
o
m
m
T> 4 -
E
o
0 ( 1 	
8/24


• sf
• ^
'A A A

\
\(
-^ 	 9 I TOLEDO HARBOR
/ surface
/
"»A A A J-
~-A A
1 1 1 1 \

8/31 9/7 9/14 9/22 9/29 10/8 10/16 10/28
DATE

-
11/14

FIGURE 5  Concentrations of dissolved organic  -N in surface water in  Little Port Walter and
            Toledo Harbor estuaries

-------
      18
      14
   Z
   i
   o>
   •o

   I

   o
   m
   n
   E

   2
   o
      10
                                     LITTLE PORT  WALTER


                                         IZ METERS
         TOLEDO  HARBOR

              METERS
                                                                       I
       8/24
               8/31
                       9/7
                               9/14
                                       9/22
                                               9/29
10/8
                                                              10/16
                                                                      10/28
                                                                                      11/14
                                       DATE
FIGURE 6   Concentrations of dissolved organic -N in 12m water in Little Port Walter and Toledo

            Harbor estuaries

-------
136
                                              LITTLE  PORT WALTER (12m)
                                          •  TOLEDO  HARBOR  (12m)
                                          O  LITTLE  PORT WALTER (surface)
                                          O  TOLEDO  HARBOR  (surface)
    8/24   8/31    9/7     9/14    9/22    9/29    IO/8    10/16    10/28   11/14   3/16/70
                                 DATE
FIGURE 7  Concentrations of ammonium -N at 12m in Little Port Walter and Toledo Harbor
           estuaries

-------
                                                                                      137
                                      DISCUSSION
The surprisingly large concentrations of NH^-N and the oxygen depletions observed in Iliuliuk Bay
indicate that the decomposition of seafood material in a restricted body of water can influence the
nitrogen chemistry of the estuarine environment. The organic waste matter resulting from seafood
processing plants located on Iliuliuk Bay is emptied into the estuary rather continuously. Thus the
highest observed  concentrations of  NH4*-N  at station  2341, 23.8 jug-atom  N/liter may well
represent the remineralization of organic material that has accumulated over a long period of time.
It would  appear  that such extremely  high concentrations of ammonium are potentially toxic to
fish (Ball, 1967}  and to other forms of life. Other effects of decomposition such as oxygen
depletion are also probably detrimental to the organisms residing in the bay.

It is important to determine whether  elevated concentrations of ammonium as were observed in
Iliuliuk Bay occur naturally in the marine environment. It appeared from the knowledge available
on the nitrogen chemistry of the sea  that it would be unlikely that such high concentrations of
NH^-N would  occur  naturally,  and  that the observed situation was therefore  the  result of
industrial  stress   on the  environment. We  felt  that  the  phenomenon  of salmon  carcass
decomposition most closely duplicated the industrial situation, and we were therefore interested in
determining  what  level  of nitrogen compounds were present  in systems where salmon  were
decomposing.

It is difficult to compare the Richards and Kletsch (1964) ammonium values for  Iliuliuk Bay to
those obtained by the Solorzano  (1969) technique in Little Port Walter, since it is uncertain what
fraction of the organic nitrogen was recorded by the Richards and Kletsch method as ammonium.
Our investigations in Little  Port Walter  suggest  that dissolved  organic nitrogen is the initial
decomposition  product and organic nitrogen (i.e., labile amino-N) may have contributed heavily to
the ammonium measured in Iliuliuk Bay. If the ammonium -N and dissolved organic -N  for Little
Port Walter are summed, a combined dissolved organic -N - ammonium -N concentration of 18.2
jig-atom N/liter occurred  near the  bottom  on 10/16/69. This approximates the value of 23.8
fig-atom of  NH^-N/liter  observed in  Iliuliuk Bay and  indicates that high concentrations of
ammonium and  organic  nitrogen  are not  restricted  to waters receiving  waste from seafood
processing.

The ammonium and dissolved organic nitrogen concentrations observed in Sashin  Creek indicate
that decomposing salmon carcasses have a significant influence  on stream chemistry. It has been
observed that survival of salmon eggs in the Sashin Creek  spawning beds was significantly lower in
the lower area of the stream. Area III, than in the upper areas. Several  reasons have  been  presented
by McNeil (personal  communication)  to  explain this  phenomenon. The  chemical parameter
normally  associated with survival of eggs in the spawning bed is dissolved oxygen, but we fee I that
ammonium or other products of  carcass decomposition might have a significant influence on egg
survival, especially when stream flow is low.

The large  dissolved organic nitrogen concentrations observed  in the surface waters of Little Port
Walter undoubtedly reflected the decomposition of salmon carcasses  occurring in  the stream and
in the intertidal zone. The bottom of  the estuary received most of the carcasses and it is here that
final decomposition occurs. Sediment  samples of the Little Port Walter estuary bottom  showed a
gelatinous quality  even  for  samples taken prior  to the arrival of the fish, suggesting that the
sediment may  act  as a nutrient sink. This gelatinous nature probably results from the long term
accumulation of fish carcasses. All sediment samples from Toledo Harbor were granular.

-------
 138


The apparent increase in the concentration of dissolved organic nitrogen observed in the control
estuary, Toledo Harbor, between September 22 and September 29 was probably the reflection of
heavy rains, wind and  heavy cloud cover which resulted both in  high run-off from, the land and
death of plankton in the water column.

It is evident that this brief study is only a beginning in our understanding of the fate of organic
matter deposited, naturally or by industry, in the marine environment/Our attempts to follow the
decomposition of salmon carcasses employing nitrogen chemistry was rewarding in  that effects
were clearly demonstrable. Since nitrogen comprises only a small proportion of the organic matter,
and since remineralization rates are slow, it is evident that more sophisticated techniques must be
utilized to  obtain a clear understanding of the process. Possibly,  remineralization of the organic
matter resulting  from carcass decomposition does  not occur within  the confined body of water
where  the carcasses are  deposited.  The early stages of  decomposition might result  in  the
production of soluble  complex  organic compounds which are transported  from the local area
before remineralization occurs.

                                 ACKNOWLEDGMENTS

This research was supported in part by Office of Water Reserach  Grant B-015-ALAS and by the
National Science Foundation Grant GB-8636.

                                      REFERENCES

Armstrong, F. A. J., Williams, P. M. and Strickland, T. D. H. (1966) Photo-oxidation of organic
     matter in  sea  water by  ultraviolet  radiation, analytical and  other applications. Nature,
     211,481.

Ball, I. R.  (1967) The relative susceptibilities  of some species of freshwater fish to poisons, I,
     Ammonia, Water Research, 1,587.

Grasshoff,  K. (1964) Zur Bestimmung von Nitrate  in Meer und Trinkwasser, Kiel. Meeresforsch,
     20,5.

Murphy, J. and  Riley,  J.  P.  (1962) A modified single  solution method for the determination of
     phosphate in natural waters.  Anal. Chim. Acta,, 27, 31.

Powers, C.  F. (1962) Some  aspects of the oceanography of Little Port Walter estuary, Baranof
     Island, Alaska. Fish. Bull., 63, 143.

Richards, F. A. and Kletsch, R. A. (1964) The spectrophotometric determination of ammonia and
     labile amino compounds in fresh and seawater by oxidation to nitrite, In Y. Miyake  and T.
     Koyama (ed.). Recent Researches In The Fields of Hydrosphere, Atmosphere, And Nuclear
     Geochemistry, Maruzen O., Tokyo.

Soloranzo,  L. (1969)  Determination  of ammonia  in natural waters  by the  Phenolhypochlorite
     method, Limnol. Oceanogr.,  14,799.

Strickland,  JJ. D. H. and Parsons, T. R.  (1965) A manual of sea water analysis (with  special
     reference to the more common  minor nutrients and  to paniculate organic material). Bull.
     Fish. Res. Bd., Can., 125,79.

-------
               PHOSPHORUS BINDING  MECHANISMS DURING
                 SELF-PURIFICATION OF  POLLUTED LAKES
                                      Jan Werner
                                   INTRODUCTION

The discharge of  sewage  into lakes and rivers gives rise to different and fundamental changes.
Among the various  parameters of importance that can influence the ecosystems, the following
three will be discussed:

    1.  The oxygen consuming substances
    2.  The phosphorus compounds
    3.  The alkalinity

The increases in phosphorus concentration and alkalinity are  two factors which are supposed to
affect  the primary production of a limnic system directly and positively (Christie, 1968; Mortimer
1941,  1942). The increased  production will, in combination with the external input of organic
substances, sometimes cause a complete depletion of  the oxygen in the bottom  waters during
periods of stratification.  The sediments will  be especially exposed to  such conditions, as the
organic particles will settle to the bottom and form  part of the upper surface of the sediment.

In this connection the exchange reactions between water and sediments seem to be of considerable
importance. The  sediments  act as large buffers and  storing places for various types  of  solid
materials. Exchange mechanisms wilt cause a shift  of certain substances between the solid and the
dissolved states. Phosphorus is  one of  the substances that  will be affected by  the exchange
mechanisms.  The fundamental experiments of Mortimer {1941,  1942) corroborate the general
experience that when oxygen is available to the sediments the transfer of phosphorus from a solid
to a dissolved state will be very limited. There will on the other hand be  an increase of soluble
phosphorus in the sediment system when oxygen is  depleted.

                          CIRCULATION  OF  PHOSPHORUS
              AND ITS ACCUMULATION  IN THE SEDIMENT SYSTEM

During summer, process 2 tends to dominate over  process 3 with an enrichment of phosphorus in
the hypolimnion and in the sediment system as a consequence. During winter, process 2 will again
dominate over process 3,  especially during the period following the formation of an ice cover. The
spring and fall  turnovers  will on the other hand  cause an even distribution of the  phosphorus
throughout the whole water mass, i.e. process 3 will be favored over process 2.

The sediment material with  which phosphorus is associated will be broken down successively to
more  simple substances  by biochemical  processes. Whether phosphorus is bound to organic
molecules or not, orthophosphate will  be  the principal end product. To reduce the amount of
phosphorus  circulating within  a body  of water,  mechanisms  causing  an accumulation in the
sediment  must be made  to operate. There are in  the  first instance two principally different
mechanisms possible.


                                          139

-------
 140
                                                         Air
                                                               Epilimnion
                                                               Hypolimnion
                 /&S/SS/S//////S///S///S////S/S//////S//S//SS//SSSSSS
                                                               Sediment
                          I. Dissolved ©—»© in biomass
                         2. P  in biomass—»sedimerting ©
                         3. Sedimenting ©—^dissolved ©


       FIGURE 1   Circulation of phosphorus and its accumulation in the sediment system


1.  An essential part of the settling organic phosphorus compounds will decompose slowly. The
accumulation according to this mechanism will reflect a dynamic equilibrium determined by the
quantity settling, the rate of decomposition,  and finally the quantity released from the sediment.

2.  Phosphorus compounds,  especially  orthophosphate, will be  bound to undefined inorganic
solids  in the sediment  system.  There will be set up a chemical equilibrium between absorbed
phosphorus and phosphorus dissolved in the interstitial water and in the water above and near the
sediment surface.

                      BINDING OF PHOSPHATE  TO FERRIC IRON

In a lake with low primary production and with a limited input of oxygen consuming substances,
oxygen will normally be available in the bottom waters.  In such a system any ferrous iron will be
oxidized to ferric iron, provjded it is not present as a very stable chelate. Ferric iron forms stable
and  partially  soluble  molecular aggregates under the prevailing conditions. These  aggregates may
have different anions incorporated, of which the following three are of special interest: phosphate,
hydroxyl  and  humic substances.  Iron is  normally present  in a large excess compared to
phosphorus. The  conditions in  the sediment may be illustrated as in  Figures 2  and 3. If ferric
hydroxide  in  the  sediment is in excess the solubility of the ferric iron will be determined by the
solubility product of ferric hydroxide. We may assume that the hydroxide exists in various loosely
crystallized modifications. The lack of defined crystallinity makes it fairly reactive. The reported
stability  constants  for ferric hydroxide range from  10~^7 to 10"44  (Feitknecht, 1959). This
reflects that the stability of ferric hydroxide  will depend on the conditions at which it is formed
and  also its age, etc. This raises difficulty when a  value relevant to the conditions in a sediment
system is to be selected. It seems reasonable,  however, that the  stability constant would be closer
to 10   than to 10   , i.e. the hydroxide should be comparatively reactive.

If ferric hydroxide is in excess compared  to ferric phosphate,  the  concentration of  soluble
phosphate  in bottom waters and its dependence  on  pH may be illustrated as  in Figure 4.  The
temperature of the  bottom water has been assumed to be about 5° C. The ionic product of water,
K>A., will then be 10    . The derived figure should be considered as an approximation as the
  W

-------
                                                               141
              Fe(+m) humic substances
Fe(+IE) hydroxide
FeMII) phosphate
        FIGURE 2  Binding of phosphate to ferric iron
1-
cr
it
0.15


0.10

0.05


0
i




Bornsjon
(oligotrophic)
Mg
028

•

-








Fe

Al








Co












Fe



1 C
PtoT°
^tot


PM




PC




>4


Albysjdn
(eutrophic)









Efi





n









Fe_|n^
ptot"
Sir167
Mg


Ca



k
r-%











Lillsjdn
(hypertrophic)

Pe_Qp
Ptot


Fe



Al
^H*.





^'=24.6


Mg

I [^£04
        FIGURE 3  Sediment analyses (Average 0 - 6 cm)

-------
 142
3
4
5
6

8
9
K)h
         12
            ^(total  P04)
            M
                        eight analyses, all below
                        detection limit
    	lower _
   detection limit
                       678
               • =  calculated  values
               o =  experimental  values
                                       FIGURE 4
IO
                                                                       II
corrections of certain  data  for temperature have not been possible. The constants used for
calculation of  the concentrations of different ionic species of phosphate have been taken from
Egan et al. (1961). The figure also includes a curve derived from an actual experiment. It appears
that the experimental curve fits fairly well  to  the  theoretically derived curve when  10    is
selected as stability constant for ferric hydroxide under the discussed conditions.

The figure indicates that:

a)   ferric hydroxide in a sediment system is of a relatively reactive type, and

b)   the concentration of soluble phosphate is highly dependent on pH, being near or below the
     detection limit under the condition expected in the system.

                  BINDING  OF PHOSPHATE TO Ca2*, Mg2* AND Al3*

Phosphate ions can be bound to ferric iron, aluminum, calcium and magnesium. Precipitation of
phosphate by calcium  or magnesium takes place only at higher  concentrations than those
discussed. At the  pH which prevails in the bottom waters, precipitate of calcium or magnesium
phosphate takes place only to a limited extent.

Aluminum will on the other hand react  with  phosphate  in a way analogous to ferric iron. The
resulting complexes have approximately the same stabilities and the same dependances on pH. As a
consequence, any  discussion of the role  of iron as a phosphate-fixing agent in sediments must
consider the possible competition between aluminum and ferric iron. This is of special importance
under conditions when ferric iron might be reduced to the ferrous state.

-------
                                                                                    143
The total amount  of  iron and  aluminum  present  at the surface  of the sediment exceeds the
phosphorus content on a molar basis more than tenfold. The fact that in spite of this a complete
fixation of phosphate in the sediment system does not take place will need careful analysis.

                    REDUCTION OF FERRIC IRON AND OXYGEN

The reduction of ferric iron must be considered with reference to the following:

a)   Fe3* is an important oxidizing agent and a redox buffer at the surface of the sediment.

b)   When ferric iron is reduced to ferrous iron, it loses its properties to bind phosphate, hydroxyl
    ions and humic substances. A physico-chemical analysis of the reaction

              Fe^+e"  Z   Fe2*      E° = 770 mVat 25°C (Schumbet al., 1937)

will give a redox value according to Nernst's equation
                                             (Fe3*!
                     EFe3*/Fe2* = 770+ 55 '°9    ^<55 mV 3t 5°C)
The Fe^-concentration will be determined by the reaction

                               Fe3*+3OH"   ?  Fe (OH)3 (s)

Fe3* will vary according to the expression
                                            10-37.0
                                            (OH')3

                   ction of water being  10"
with pH according to
With the  ionic production of water being  10'     at 5° C, the ferric ion concentration will vary
                      (Fe3*) = 10'37>0+ 3-14.7 - 3 pH = 10*8'6 ' 3 pH

If the concentration of Fe2* is assumed to be 10   M (0.6 ppm) and if we use the expressions for
Fe3* and Fe2* given by Nernst's equation the following expression will result
                                                    1(f8.6-3pH
                          EFe3*/Fe2+= 77° *  55 log	
                                                         10'5
Epe3»ype2+ as a function of pH is given in Figure 5.

Oxygen may be reduced in the following way:

            1/2O2+H2O+2e"  £  2 OH'    E° = 401 mVat 25°C (Latimer, 1952)

The redox potential varies according to
                                                55     PO-,
                              E02/OH'  = 401+—log

-------
 144
The 02/OH" system will be the determinant for the oxidation or reduction of iron.

PQ  is given as the partial pressure of oxygen. The oxygen content in the atmosjahere is 21% of
volume giving  PQ  = 0.21 atm. At saturation in fresh water and at 5° C this corresponds to an
oxygen concentration of  12.5 ppm. Henry's law gives

0.21 = K -12.5      K =  0.0168

Po = 0.0168 (O2 ppm)

We introduce this expression into the above Nernstian expression and obtain
                                55    (02 ppm)
                                                     See Figure 5
At a low oxygen concentration, e.g. 0.1 ppm, EQ /QH~ varies in the way indicated in Figure 5.
From the values given in this table the following conclusions can be drawn:

a) Also, at as low an oxygen concentration as 0.1 ppm the resulting redox potential will cause
ferrous iron to be oxidized to ferric iron.

b) The ferric hydroxide  will be more stable at higher pH than at lower pH, as is seen from the
difference between the two redox systems shown in Figure 5.
                       56789
                         :• = 770*55 log tj£*r] ; [Fe3*] = I06>l

                                                  [021 in ppm

                                        FIGURE 5
10   p
ft

-------
                                                                                     145
        CHEMICAL  DIFFERENCES  BETWEEN FERRIC AND FERROUS IRON

It might be of value to use the generalizations of Ahrland et al. (1958) who have outlined some
fundamental differences between hard and soft metal acids. The hard metal acids tend to be in a
high oxidative state and  have their electron shells tightly bound to the atomic nucleus. The
electrons are  less able to  polarize and  the  chemical  bonds formed  by these  ions and  their
counterions show a high degree of ionic bonding. Typical hard acids are Mg2+, Ca2+, AI3+ and Fe3*.
The H* ion  also shows the characteristics of a hard metal acid.

The soft metal acids are characterized by  no oxidative state, or a low one. The electron shells are
larger and  more polarized  and the chemical bonds also tend to be more polarized, leading to a high
degree of covalency. Typically  soft acids are Cu+, Cd2+, Hg2+ and Hg2+ . Fe2*, Cu2+ and Zn2+ show
characteristics that place them  in between the hard and the soft acids. In their relations to anions,
the hard and soft acids react differently. The following sequences of stabilities of complex ions are
often found (Fig. 6). The  atoms in the figure are assumed to be incorporated in the active sites of
the anions.
                             Hard Metal Acid:    N>P>As>Sb>Bi

                             Soft Metal Acid:   N

As>Sb>Bi Hard Metal Acid: 0>S>Se>Te Soft Metal Acid: O<5~Se~Te Hard Metal Acid: F>CI>Br>l Soft Metal Acid: F


-------
 146
                  Fe2*
                                        ^*P- poor
                      I.  oxidation  Fe2**02—»Fe3*
                      2.  oraanic-P Hcttrlg»po4
                      3.  Fe3** PQj—* FePQ.   precipitate
                      4.  nettodiffusion of P04

                                        FIGURE?
                                                                water
                                                                oxidative
                                                                  zone
reducing
  zone
                    pH-DEPENDENCE OF  FERROUS  PRECIPITATES

Any tendency  to form  insoluble ferrous  compounds during the establishment of anaerobic
conditions in the  sediment will cause the oxidation - from a kinetic point of view - to regress to
ferric iron during instances when aerobic conditions are reestablished. The  carbonate and sulfide
are important in this connection. The solubility product of FeC03 is given by

                                 (Fe2+)(CO|') = 10't0'7

The carbonate  is  in equilibrium with hydrogen carbonate and carbonic acid. The  solubility of
FeCO3 will thus be a function of pH as shown in Figure 7 (Weber, Stumm, 1963).

FeS reacts in the same way, the solubility of which is

                                   (Fe2+)(S2-)=10-19'3

The sulfide is in equilibrium  with mono- and dihydrogen sulfide. The solubility of ferrous sulfide
will vary with pH as is shown  in Figure 8 (Hutchinson, 1957).

The above stresses the fact that the stabilities of all major ferrous compounds that are present in a
sediment system will  be functions of  pH. It  may be assumed that the combination of ferrous ions
with any organic matter present in the sediment will follow  the same general  rule.

The following  will take  into  consideration how  the alkalinity of the total  lake system  will
influence the equilibria outlined above.

-------
                                                                                     147
             ROLE OF HYDROGEN  CARBONATE AND CARBONIC ACID

The pH of a lake system is influenced by a variety of factors. These include biochemical processes
and exchange reactions between the atmosphere and  the water and between the water and the
sediment. The carbonate  system will normally cover around  90% of the total buffer capacity.
Organic matter of different origin will  cover the remaining part. pH varies around pH 7 according
to the relation
                                             {HCO-3)
                              pH = 6.52+ log
                                            (H2C03)
                           at 5° C
Discharge of  sewage  will  increase  not only the phosphorus concentration but in  addition the
concentration of bases. These bases are transformed into hydrogen carbonate by biochemical
processes either in a treatment plant or in the receiving water. The increase in hydrogen carbonate
concentration will raise the pH according to  the above expression. A higher pH of the total mass
will thus result. The change  in alkalinity will influence both the trophogenic zone  and the
                        0

                        2

                        4

                        6

                        8

                        10
                         2      4       6       8      10     12  pH

                           Solubility of Fe2*  = f(pH) (10) in  l(T3M  C03
                        0
                        2

                        4

                        6

                        8
                        10.
                      H2Sfofal -ICPM
2       4      6      8

Solubility of Fe2* = f(pH) in

               FIGURE 8
                                                        10      12  pH

                                                           H2S

-------
 148


sediment system. The influence of pH on the redox potential of the 02/OH" and the Fe3+/Fe2+
systems,  upon the binding of phosphate  to Fe3* and to AI3+ and upon the solubility of various
Fe2+- precipitates has been mentioned previously. Moreover, all the trace elements will probably
act in a way analogous to Fe2* by being less soluble at higher pH.

The  theory discussed  in this paper illustrates that  in  order to enhance the capacity  of  the
sediments to act as a sink for phosphorus, advantage could be taken of the fact that the binding of
phosphate to ferric iron and to aluminum will  increase in stability when the pH  is lowered. The
validity of this was tested previously for  the total organic production in a series of experiments
where the alkalinity of a nutrient-rich water was changed by the  addition of controlled quantities
of acid (Werner, 1969). The addition of acid-reduced hydrogen carbonate by partially replacing it
with CI" or SO|*. The results obtained clearly indicated that the  primary production depends  on
the alkalinity and the pH, among other factors.  Lowering of the alkalinity was accompanied by an
approximately linear decrease of production, measured as the total amount of organic carbon. The
following will  describe supplemental experiments where the  reactions of a sediment system  to
changes in the hydrogen carbonate concentration and the pH have been examined.

                                    EXPERIMENTAL

Sediment and water were taken from the hypertrophic lake Lillsjon near Stockholm. The lake was
heavily polluted by municipal sewage. The sediment was taken  from the bottom by an Ekman
dredge and the water was taken with a Ruttner sampler. The time of sampling, 6th of October,
coincided with  the fall turnover.  19% supersaturation, combined with a high  pH, indicated that
biological production was still taking place. Table I  gives the analytical data of the sediment and
the water sample.

50 ml of sediment and 450 ml of water were added  to each of 24 - 500 ml Erlenmeyer flasks. The
flasks were divided into six series and known amounts of 0.1000 M HCI were added to each group.
The flasks were shaken  slightly and kept at room  temperature. Illumination  was made so as to
simulate  the light conditions during fall circulation. The added amounts of HCI  are shown in Table
                                         TABLE!

                             Analysis of:
                   Sediment

                     suspended matter                       50.3 g/1

                     total organic carbon                      1.4 g/1
                     total iron                                1.0 g/1
                     total phosphorus                        0.108 g/1

                   Water

                     dissolved oxygen                        13.7 mg/1
                     temperature                            8.8° C
                     pH                                      9.1
                     alkalinity (HCO,)                     1.58 mekv/1
                     total organic carbon                     17 mg/1
                     total iron                              0.120 mg/1
                     total phosphorus                 .      0.500 mg/1
                     phosphate                             0.235 mg/1

-------
                                                                                       149
2. Visual inspection showed that the suspended  matter settled much faster in the flasks with the
largest amount of acid added: series 1  and 2 more than series 3 to 6. There was a difference seen
within series 3 to 6, the matter in series 6 settling more slowly than in series 5, etc. This is what
was expected. The added hydrogen ions  neutralized excessive negative charges, thus making the
repulsion between the particles less efficient. The particles agglomerated and settled more easily.

The aqueous phase was analyzed  on  day  11 (Table 2). Each  value  was the average  of four
replicates. It appears from this table that  the  alkalinity has decreased somewhat irregularly. This
may be explained by the slow rate of certain reactions in which the solid phase takes part. Calcium
and magnesium have partly been replaced by hydrogen ions, thus appearing in the aqueous phase.
The  iron  is  probably  associated  with  colloidal  or dissolved substances. Finally,  the total
phosphorus concentration has decreased in all the flasks.
                                         TABLE 2

                               Analysis of Water After 11 Days


                                                              Total
Series        Added Acid         Alkalinity         Fe          P          Ca          Mg
               mekv/1            mekv/1          jzg/1         jug/1         mg/1        mg/1
  1              1.80                0            550         286         24.4         6.6
  2              1.44                0            600         288         21.2        6.05
  3              1.08              0.30           600         245         18.9        5.80
  4              0.72              0.52           620         243         17.4        5.48
  5              0.36              0.95           680         242         15.2        5.35
  6               0                1.55           740         267         14.4        5.35


The flasks were placed in the dark at  20° C and covered with a  membrane. This  limited oxygen
diffusion in the water, thus simulating the conditions in the near bottom water and the sediment
during a period of stagnation. The elevated temperature was selected in order to speed up certain
reactions. Oxygen and pH were analyzed after a total of seven days in the dark (Table 3).

The flasks were analyzed again after an additional period of 31 days in the dark under the same
conditions (Table  4).

The iron concentration had dropped considerably in all instances, and could be detected only  in
the series  having  the  alkalinity  reduced  to zero.  In the series with a measurable alkalinity, the
alkalinity had decreased in all instances. One of the reactions that probably had taken  place in the
sediment, causing  the alkalinity to decrease, is the following:

                      FeS+9/4O2 + 2OH'+ 1/2 H20-" Fe (OH}3 + SOl'

The pH values in  the extreme series  1  may very well be considered only of interest as illustrations
of the discussed  theory, as may  be  those  of series 2 and 3. The concentration of hydrogen
carbonate  is zero in these  series. The values  for oxygen indicate  that bacterial decomposition of

-------
 150

                                      TABLE 3

                      Analysis of Water After 7 Days In The Dark

                                                                                      02
Series                                       pH                                       mg/1
  1                                        4.50                                       4.1
  2                                        5.31                                       4.2
  3                                        5.45                                       3.3
  4                                        6.45                                       4.5
  5                                        6.83                                       4.0
  6                                        7.15                                       4.8
the organic* continues in  all series. A consequence is that carbonic acid and carbon dioxide are
present in excess. In accordance with theory, the phosphorus concentration shows the largest drop
in the series having no alkalinity and a low pH. Also the series having a measurable alkalinity shows
an apparent  relationship between the parameter and the phosphorus concentration. The lower the
pH of the water the less phosphorus will be in solution (Fig. 9), thus indicating that phosphorus
will be absorbed by the sediment system in a direct dependance upon pH when aerobic conditions
are maintained.
It is felt that the above discussion  and the  results reported may assist in the interpretation of the
phenomena associated with the discharge of sewage to natural waters of different types concerning
alkalinity and character of sediment system.
                                        TABLE 4

                        Analysis of Water After 40 Days In The Dark
                                        Total
Series         Alkalinity
                mekv/1
  1                0
  2                0
  3                0
  4               0.32
  5               0.85
  6               1.44
Fe
AtgA
170
60
30
trace
trace
trace
P
jug/1
10
16.1
24.4
79
92
112
P04-P
J"g/l
10
13.2
18.0
61
84
108
PH
4.1
4.8
5.3
6.1
6.6
7.0
02
mg/1
2.35
1.73
2.02
1.73
1.50
1.60

-------
• =
P04
total P
                      FIGURES

-------
152
                                     REFERENCES

Ahrland,  S.. Chatt, J.. Davies, N. R. and Quart, Rev. (1958) (London), The relative affinities of
     ligand atoms for acceptor molecules and ions. Vol. 12, p 265.

Christie, A. E. (1968) The Ontario Water Resources Commission, Div of Research, Publ. No. 32.

Egan, E. P. Jr., Wakefield, Z. T. and Luft, B. B. (1961) Low temperature heat capacity, entropy
     and  heat of formation of crystalline and colloidal ferric phosphate dihydrate, J. Phys. Chem.,
     65, 1265.

Feitknecht, W. (1959) Z. Electrochem., 63,1979.

Hutchinson, E. G.  (1957) A Treatise On Limnology, Vol. I, 760.

Latimer, W. M. (1952) Oxidation Potentials, 2nd Edn, Prentice-Hall, New York.

Mortimer, C. H. (1941) The exchange of dissolved  substances between mud and water in lakes, J.
     Ecology. Vol. 29, p 280.

Mortimer. C. H. (1942) The exchange of dissolved  substances between mud and water in lakes, J.
     Ecology, Vol. 30 p 147.

Schumb, W. C.,  Sherrill,  M.  S. and Sweetser, S. B. (1937) The measurement of the molal
     ferric-ferrous electrode potential, J. Am. Chem. Soc., 59,2360.

Volleuweider, R.  A. (1968) Organization for Economic Cooperation and  Development, Paris
     DAS-CSI-68.27.

Weber, J. W.. Jr. and Stumm, W. (1963) Mechanism  of hydrogen ion buffering in natural waters, J.
     Am. Wat. Works. Assn., 55. 1553.

Werner. J. (1969) Havsforskarmotet i Lund, Paper No. 18.

-------
         CRITICAL REVIEW OF  PAPERS ON RECEIVING WATERS
                                     Peter A. Krenkel
                                    INTRODUCTION

Temperature has profound effects on biological, chemical, and physical processes. It is particularly
appropriate to investigate these effects under cold weather conditions, inasmuch as a paucity of
information exists regarding waste treatment and water quality management in the Arctic.

The organizers of  this conference are  to  be commended  in gathering together such an eminent
group of scientists and engineers, and it is a great honor to have the opportunity of discussing a
portion of the papers presented.

I have attempted to be as objective as possible in the following discussions, and it is hoped that the
authors involved will accept my comments as constructive discussion rather than criticism.
        Synoptic Study of Accelerated Eutrophication in Lake Tahoe, California-Nevada

                                     Charles Goldman

 Lake Tahoe is probably one of the most beautiful lakes in the world and changes as described by
 Dr. Goldman  are quite  obvious to me, since I spent many days there some 20 years ago. The real
 problem is, of course, people.

 Measurements  included  primary  productivity  of  phytoplankton  and periphyton,  species
 composition,  biomass, and biotic diversity. I  believe the productivity information  is of particular
 significance inasmuch  as the methodology utilized appears to yield maximum information  in a
 minimum of time and effort.

 The results of the study demonstrate the effects of the added nutrients on the receiving water and
 certainly demonstrate the need for control measures.

 The author is to be complimented on the analysis of his data. There is little doubt that the future
 of water pollution  control will dictate more  quantitative work from the biologists, as is the case
 with Dr. Goldman's work. The use of statistics and parameters, such as a species-diversity index,
 are to be encouraged.
                                            153

-------
 154


                The South Basin of Lake Winnipeg - An Assessment of Pollution

                                Jo-Anne M. E, Crowe, Canada

The author has presented data in an attempt to demonstrate that Lake Winnipeg is suffering from
an increase in the rate of eutrophication. Three indices were utilized in this endeavor; physical and
chemical measurements, benthic organisms, and fish.

There is little doubt  that the lake, as described by the author, is suffering from  the effects of
pollution; however, the data presented is not conclusive with respect to changes noted in severely
affected eutrophic lakes. It  is unfortunate that no measurements of phosphorous or nitrogen were
available that could be assessed for their role in the apparent changes occurring in the lake.

The author mentions the severe oxygen depletion noted in the Lake Erie basin and the increases in
various  ionic  species indicative  of the  conditions in that  basin. She then states that dissolved
oxygen  values in the  lake are usually  above 80% of saturation and that the only ionic component
showing an increase  was calcium. The  Secchi disc readings were significantly reduced  in  the
39-year period, however.

Examination of the data fails to reveal significant differences in the chemical measurements at first
glance,  even of calcium. It would be interesting to subject the data to a statistical analysis in order
to determine  the  statistical significance of the changes,  if any,  on a  quantitative basis. Mere
comparison  of averages means little with this type of  data. Differences in sampling techniques
should also be accounted for.

Measurements of the  phytoplankton would  have been interesting, as would discussion and analysis
of some of the chemical data.

The only really significant changes that  were noted were an increase in benthic density, a shift to
more tolerant forms  of bottom  organisms, and a  decrease in the fish catch.  Again, a statistical
analysis of these factors  would be of considerable value  in determining the real significance of
these changes.

Another informative evaluation  of the  data would be to utilize some form  of species diversity
 index with respect to the bottom organisms, which will be mentioned  later.

While the fishing yield has  been  significantly reduced, the author states  that this reduction could
 be attributed to "over-fishing" and the use of illegal methods.

 An additional point  of interest  is the possibility of mercury playing a role in the change in the
 benthos. The toxicity of  mercury is extreme, and if the concentrations in the fish have "exceeded
 0.5 ppm", one cannot help but wonder what the concentrations might be in the organisms being
 ingested by the fish.

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                                                                                     155


                 Eutrophication in Some Lakes and Coastal Areas in Finland
                         With Special Reference to Polyhumic Lakes

                               Pasi O. Lehmusluoto, Finland

A good review of the phytoptankton production in Finland and in arctic areas was presented by
Dr. Lehmusluoto. He points out that in Alaska, almost half of the annual phytoplankton primary
production  may occur beneath the ice sheet in  the spring  time.  He suggests  that the mean
maximum primary production  rate per unit volume  in the growing season measured in situ, or in
constant light, should be used as an index for the many kinds of water bodies to give a relative, but
objective, index for the phototrophic level of the water. It is also demonstrated that the direct
comparison of trophic states of humic and nonhumic lakes is impossible, as the classification  of
polyhumic lakes on the basis of phytoplankton production cannot give an objective result.

Polyhumic water in Lake  Hakojarvi showed that nitrogen was the primary  limiting nutrient and
was also a primary limiting nutrient for bacterial growth. The addition of nitrogen and phosphorus
caused a large algal  growth.  Seven in  situ plastic  test cells were used, the cells being  ten meters
deep,  1.2  meters in diameter, and having open tops  with a  water  volume of 12 m3. Nutrient
additions ranged  from  0.05  to  1.0 mg/l  nitrogen  and  0.005 to  0.1  mg/l  of phosphorus.
Phytoplankton primary production was measured by the carbon  14 method. Phosphorus alone did
not cause significant eutrophication and  there were not any large changes when only nitrogen was
added. In the cells where both nitrogen  and phosphorus were added, the  greater  the addition  of
nutrients, the larger the increase in the phytoplankton production.

Humus may be important in the total production of polyhumic waters due  to light extinction. It is
also proposed that humus, as  such, or transformed to bacterial biomass, may serve as food for
zooplankton and,  thus lead to relatively high  fish production.  It should  be noted that bacterial
numbers in humic waters are normally comparable to numbers in eutrophic lakes.

In Lake Saimaa, phytoplankton production has been studied.  The lake receives 1,200 m3/day of
biologically purified domestic sewage and  260,000 m3/day of mechanically purified pulp mill
waste, which is  44% sulfite and  56%  sulphate liquor. The domestic sewage stimulated the algae
growth. Pulp mill effluents were almost lethal to algae at 10% effluent concentrations, and in 1%
and 0.1% effluent concentrations, the algae growth was  slightly stimulated. Pulp mill effluents
seemed  at first  to  hinder  phytoplankton  primary   production,  but  caused pronounced
eutrophication about 9 km from  the  outfall. Both domestic sewage  and pulp mill effluents do
cause eutrophication.  The maximum eutrophication caused by the pulp mill effluents is  more
intensive than that caused  by the domestic sewage, though it occurred far from the discharge area.

Eutrophication is a problem in the coastal area in Finland, as well as in lakes. The major problems
are near the cities on the coast and are important recreational areas. Blue-green algae  blooms
occurred during late summer and restricted the use of the waters.

The phytoplankton production 1 km from the outfall  was about 30 times higher than that at  12
km distance from the  outfall. Annual primary production near the outfall was 5 times higher than
in the unpolluted areas.

In conclusion, it is important  to  consider all the possible efforts to  reduce nutrient input into
receiving waters, in any form, in order to avoid overeutrophication, of waters.

-------
 156
It would be  interesting to hear  the speaker's comments on the recent hypothesis of Knentzel,
which has caused considerable concern in the U. S.

Knentzel (1969) concluded  that  phosphorus and nitrogen were  not the  limiting factors in
eutrophication, but instead, organic material and the resulting production of CO2  by bacteria.
Knentzel's conclusions were based on the following observations:

     1.   In natural water, blue-green algae and bacteria are always found in close association.
         Separation is detrimental  to algae.

     2.   Massive algal  looms are  always associated with  excessive amounts of decomposable
         organic matter.

     3.   CO2 is the major nutrient for algal growth. 2 gms CO2 are required  for one gram algae.

     4.   Large  amounts of CO2 required  cannot  come from the atmosphere or land-dissolved
         carbonate salts.

     5.   Bacteria can supply 20  mg/l CO2.

     6.   P is widespread in nature and algal blooms have been documented where P< 0.01 mg/l;
         and no blooms have been documented where P > 0.01 mg/l but no organics.

It is  interesting to note that recent  work by the Federal Water Quality Administration Laboratory
in Athens, Georgia, appears to lend  credence to Knentzel's theory (Kerr, et al., 1970).
               Observations on the Recovery Process in a Lake which had Earlier
                         Received Waste from an Ore-Dressing Plant

                                   Bengt Ahling, Sweden

The objective of this paper was to compare the physico-chemical and  biological parameters of
Lake Balsjon in  Central Sweden before and after the shutdown of an ore dressing plant. Initially,
the parameters from Lake Balsjon were compared to a control lake before shutdown. The question
asked was "Can  a recipient of some waste satisfactorily recover, purify itself to the point at which
its water can be used for more desirable purposes, within a reasonable time?"

The ore dressing plant's principal ores were hematite and magnetite. The process involved gravity
and wet-magnetic concentrations, hence large amounts of iron were deposited in the lake.

Table 1 shows a comparison of the physico-chemical parameters presented in this paper.

The most interesting part of the paper, and possibly the most important factor, is the development
and changing of the ecosystem within the lake. Originally the lake was a 'sterile milieu'. Initially,
there was a  noted absence of sessile living lake-bed organisms and submerged plants which was due
to the reduced penetration of sunlight. No zooplankton were found whatsoever.

-------
r*.
tn
                                                       TABLE 1
             Parameter
            Before

  Control Lake     Lake Bal
                           After

             Control Lake        Lake Bal
                                 Comments
              1. Turbidity

              2. Colour


              3. Secchi disk
                 transparency

              4. pH
             5. Conductivity
             6. Total iron,
                 mg Fe/1

             7. Oxygen
             8. Consumption of
                 permanganate
                 mgKMn04/l

             9. Nitrogen and
                 phosphorus
<100 ZP units >1000 ZP units  100 ZP units

  30 mg Pt/1     650 mg Pt/l     30 mg Pt/1
  2-4 meters   Few centimeters

                 7.8 -8.1*
                7 times the
                control lake
              3 meters
     <5
     20
 1-10

90% sat
  10
              400 ZP units

               30 mg Pt/1



                2 meters

        Reduction in pH (spring)
          Increase in pH (fall)


         3 times the control lake



                  ,5

                Still high
30
30
              Returned to
               normal hue

              Due to reduced
               turbidity

              Primary production
               Increased which
               increases pH

              Actual values
              undecipherable
Bottom sample
 showed oxygen
 deficit down to
 17%

Increase showed
 increaise in organic
 material in lake

No change
No values reported
 in paper
              * After dilution with Lake Balsjon waters

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158


After the plant shutdown, consequently reducing the turbidity of the water, the lake was again
suitable  for  biological  growth.  The  occurrence of phytoplantkon  was markedly increased,
especially diatoms. Organisms that were completely absent initially began to appear in abundance,
e.g.  chrysomonad rhodomonas and  dinobryon  divergens. Besides increasing  the  number of
individuals in  a  species, the number of different species  increased. Two years after the  plant
shutdown the composition of zooplankton was almost identical to that of the control lake. Also, it
was noted that fauna normally living on the lake bed was in the process of being built back up.

After observation of the physico-chemical  parameters, one is led to believe that Lake Balsjon is
returning to its normal state as compared to the control lake. However, the values reported in the
paper are very general in most respects. Yet, the building up of a balanced biosystem is quite
evident by the changing biological picture. Not only  is the number of individual species increasing
but the number of species is also increasing. Therefore, one can conclude for this particular lake
that the physico-chemical aspects are returning to a normal  pattern slowly, while the ecosystem of
the lake is returning to a balanced system much faster.

As previously mentioned, the  use of  some form of a "Species Diversity Index" for comparative
purposes would add considerably to the conclusions that could be made from this  study.
         Depletion of Oxygen by Microorganisms in Alaskan Kivers at Low Temperatures

                                  Ronald C. Gordon, USA

 This paper demonstrated that bacterial degradation occurred in subarctic rivers at temperatures of
 0° C to 20° C. As the incubation temperature was decreased, a lag phase increased, but extensive
 metabolic activity was observed at all temperatures.

 The rate also decreased with decreasing temperatures as might be expected. The rate of activity
 was affected by the nature of the substrate, primary effluent, and rapid D.O. depletion was shown
 at all temperatures, while secondary effluent showed activity at 10° C and 20°  C but none at 0° C,
 probably indicating  the  effect  of nitrification, i.e., the high  temperature dependency for
 nitrification yielded no growth at 0° C.

 Psycrophillic bacteria grow well at low temperatures, but the rate  of activity increases with
 increasing temperature.

 It is obvious that the 5-day 20° C BOD test is not a good measure for pollution control at low
 temperatures because of possible different mechanisms of metabolism. It would appear that the
 "yardstick" for pollution in cold regions should  be some form of total carbon analysis or at least
 that the BOD values measured should be at the temperature of the receiving water.

 One wonders why the author did not extend the data analysis to include determination of the
 effects of temperature on the rate constants and a comparison of the rate constants themselves. It
 would appear that the data required for this information has already been acquired and  all that is
 needed is some mathematical analysis and then a quantitative presentation of the results.

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                                                                                     159


This information would be quite useful inasmuch  as  the  characteristics of the oxidation rate
constants at low temperatures need elucidation.
       Prediction of Dissolved Oxygen Levels in the South Saskatchewan River in Winter

                                 Robert C. Landine, Canada

This paper is interesting inasmuch as some  of the differences  in stream analysis in cold climates
over warm weather conditions are discussed. The low temperatures, ice cover, lack of local inflow,
high oxygen saturation values  and  low reaction rates are  all different  from  those  usually
encountered.

The  approach described is  more  or  less a  standard one, with modifications for cold weather
treatment. It should first be pointed out that utilization of this type model  requires steady state
conditions, an assumption that is rendered invalid because  of  the  hydroelectric power  plant
operations.

In addition, the goodness of fit of the  proposed model is questionable inasmuch as 4 sampling
points are hardly sufficient for a 202 mile reach. Also,  since the change in Dissolved Oxygen was
less than  1 mg/1  in ~12, almost any coefficients would produce a fairly good fit with the relatively
low  organic loadings used.  Thus, there is  no  assurance that the model  will  accurately predict
effects of major changes in flow and/or loading conditions.

The apparent anomaly wherein  the assumed values  of Kj had  a negligible effect  on  the
deoxygenation rate  in the river was partially due to the incorrect assumption  that the bottle Kt
was  identical to the river deoxygenation coefficient, Kr. This is very seldom true  inasmuch as
oxidation  in a bottle  is hardly similar to that occurring in a river.

The ultimate first-stage BOD is a fixed  parameter and should  be  determined independently by a
long term BOD  test. It can  be estimated from short term BOD's if the bottle coefficient, KI, is
also determined. L is not a function of Kj as implied by  the author. Once L is determined, the rate
of deoxygenation in the river is  assumed  to  be  proportional to L and K^, which  should be
determined in the river.

It should also be noted that the author's use of the English reaeration equation will probably not
be adequate for  the conditions of  the Saskatchewan River. This equation was  empirically derived
from very small  streams and brooks and has been shown many times to be  inapplicable to rivers
the size of the Saskatchewan. If the author had to use an equation of this type, he would have
better success (optimistically) using Churchill's equation (1962):

                                 k2 =  5.026 U'

which was derived from what is considered  to be the best stream data ever  taken. In either case,
the use of empirical  equations should be subjected to extreme cases in order to avoid gross errors.

The author might well have  applied a more  rational equation  such as  the  one progressed  by
Thackston & Krenkel (1969):

-------
160
                               k2  = 0.000125 (UF1/2)U.
                                                        h

                                      U
                                 F =	      0^ =  hSeg
                                      9"
which has a theoretical base and has been successfully used in field measurement.

The comments herein should  not  detract from  the  effort put forth  by the author inasmuch as
obvious limitations were  imposed because of a lack of adequate time  and funds. As is the case in
many water quality investigations, the results must be in accord with economic limitations of data
collection.
             Pollution - A Biological Study of Some Receiving Waters in Hokkaido

                                  Matsunae Tsuda, Japan

The objective of this paper was to study the pollution effects on the  biota of the Ishikari River.
The paper gives a fairly  good descriptive and qualitative piece of work but gives no real definitive
idea of the total effect on the biota, the degree of damage, or any way of comparing this data with
other work.

A  major weakness in the paper is that the writer has but one source to  compare and give
background to the study. A major aspect appears to be concerned with population dynamics. It
should be  noted that in 1964, Silvey and Roach published a  definitive paper  on population
dynamics in fresh water systems using ten years of accumulated  data. There has been a great deal
of  work dealing with species diversity as related to pollution perturbances. Two fine papers were
published by Odum, et  al. (1963), and Pearson (1967), and demonstrate the variances  of species
diversity attributed to various pollutants.

The author did mention how and with what equipment the data was taken. Since no reference was
made  to sampling  techniques and methods of analysis, scientifically,  this data has little meaning
either qualitatively or quantitatively.  It is obvious that sampling and analysis  techniques should be
described so that the degree of accuracy and precision of observed data may be ascertained.

If the microbenthotic organisms were analyzed by a microscope, the species  diversity could easily
be  obtained. This would yield a somewhat quantitative answer rather  than the qualitative answer,
"There were  numerous  organisms or  just a few  species were  observed". A common species
diversity formula used is:
                                     1 = -Sj Pi Loge Pi
       where Pi = n-t/n
              n. = number of individuals per species
              N = total number of species

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                                                                                     161
When working with microorganisms such as  zooplankton,  etc., Copeland (1966) used a simpler
method to obtain a species diversity, which is:


                          I =  number species/1000 microorganisms

It is  also of value to determine some  abiotic analyses such as TOC, BOD, COD, and dissolved
oxygen,  in order to obtain a better picture of the water quality. This additional information would
allow interpretation of the biological data with greater significance than only qualitatively.
          Chemical Effects of Decomposing Salmon Carcasses on Aquatic Ecosystems

                           David Brickell & John Goering, U.S.A.

The authors have presented some interesting data in an attempt to explain a most complex system.
The toxic nature of ammonium ions in the water is certainly of concern; however, the authors did
not measure  pH, which  has  a rather drastic effect on  this toxicity.  It is possible  that a high
concentration of ammonium  ions  at  a low pH value will be amenable  to fish life, but if the pH
value is increased the toxicity will probably increase. It has been reported that the toxicity of a
specified concentration of  ammonium compound  tested with fishes increased  by at least 200%
between pH 7.4 and 8 (1937). It should  also be noted that the toxicity of ammonia is reduced in
the presence of CO2 and increased with low concentrations of oxygen.

The  authors  did  not mention the  stratification occurring in some of the  sampling  areas.
Examination of the temperature and the salinity data demonstrates density differentials sufficient
to maintain a rather stable stratified flow  regime. This would help to explain the observed
increases in nitrogen and decreases in oxygen  that occurred at  these lower levels. With the new
emphasis  on  water pollution control, the  nitrogen  problem will become  more significant as
increased  treatment introduces effluents of  a more  stabilized  carbonaceous water  and  readily
available organisms that can oxidize ammonium to nitric and nitrite to  nitrate. It would therefore
be quite useful for the authors to attempt to quantitize the nitrogen phenomena that is the subject
of their paper.

Since it is an autocatalytic reaction, nitrogen transformation can be described by:

         dc
         d7=KC(N-c)

       where: C = concentration of ammonium or nitrate
             N = concentration originally present
             K = reaction  coefficient

Wezernak  and Gannon (1968) have utilized  this model with success on several receiving waters.
Knowing the  time  of passage, samples are collected at a minimum of three points in the study
section. One sample is collected at the beginning of  the study section to determine the  upper limits
of ammonium and  nitrite oxidation and to determine the amount of inorganic nitrogen oxidation
between the starting point and the other two stations. Of the remaining two samples,  one is taken

-------
 162


near the beginning of the study section and one near the end.

The effect  of  temperature on the  process is evidently  quite pronounced  inasmuch as lower
temperatures appear to significantly decrease the rates of nitrification.  It would be interesting to
observe the  rate constants for the nitrification processes under the cold conditions of this study.
Optimum temperatures for the nitrifying bacteria have been reported in the range of  28° - 36° C,
considerably above the temperature of this study.
   Self-Purification of Polluted Lakes in Temperate Regions - Phosphorus Binding Mechanisms

                                    Jan Werner, Sweden

The author discussed a mechanism for  phosphorous removal in lakes. By using solubility products
and thermodynamic relationships, he concluded that ferric ion will be the dominate species of iron
in oxygen-containing  waters, and ferrous ion  will dominate in  oxygen-deficient regions. He also
discussed the pH dependence of ferrous precipitates. It was concluded that phosphorous removal
could be improved by a lowering of the pH to 4 because of the  increase in stability of the binding
of phosphate to iron. These conclusions can also be found in work by Morgan and Stumm (1964),
Hem and Cropper (1959), Anon. 0970), and others.

It should be noted that a substantial fraction of iron in lake waters is present in suspended form
and the insoluble ferric ion sediments into the hypolimnetic waters. The rate of sedimentation is
influenced by many factors, probably the most significant being the  colloidal chemical nature of
the ferric precipitate.

The ferrous  ion may  be  soluble up to  a few mg/l, depending on alkalinity and pH and is of
significance  in the oxygen-deficient hypolimnion.  The ferric  ion not reached in the overlying
waters will be reduced at the mud-water interface.

The progressive accumulation of phosphate in the hypolimnion may  be  partly attributed to
plankton, but other  factors are involved. There is  usually more iron than  phosphorous in lake
water, leading to the formation of ferric-hydroxy-phosphate in the upper waters immediately after
circulation.  Hutchinson  (1947)  has reported  that an  oxidized  mud  surface  not only holds
phosphate but prevents diffusion of phosphate from deeper mud layers, as ferrous iron is always in
excess and when oxidized, precipitates the phosphate.

The author  did not mention the amphoteric properties of ferric hydroxide, which may play a role
 in the process: Isoelectric point at a pH = 5.5, pH > 5.5 the species is more negative, pH < 5.5 the
species is more positive. Also, the various exchange mechanisms in the  sediment and on the
hydrous metal oxides should be investigated. Since  silicates interact with iron in a manner similar
to phosphates, their role should be elucidated.

The author also failed to  take  into account the species  change of the inorganic phosphate with
changes in pH. At very low pH's, H3PO4 is the major species, at approximately a pH of 4, H2PO4"
is the major species, and so on until at pH's of 11 to 13, orthophosphate becomes the predominate
inorganic phosphate species. At a pH of 4, the ferric cation will not precipitate as FeP04  but as
 Fe(H2PO4}3, and this precipitate will  have a completely different precipitation solubility product

-------
                                                                                    163

tfian ferric phosphate. In a chemical sense, we are dealing with a dynamic and unsteady system,
and, therefore, the rates of precipitation equilibrium studies carried out in this paper.

Finally,  the  influence  of biological activities on  the chemical  reactions described  should be
investigated.  There  is  little doubt  that  the  biota plays a significant  role in determining the
distribution of chemical constituents in a lake.
                                      REFERENCES

Anon. (1970) Chemistry of nitrogen and phosphorus in water, J. Amer. Water Works Assoc.

Churchill, M. A. (1962) The  prediction of stream reaeration rates, Tennessee Valley Authority,
    Cattanooga, Tennessee.

Copeland,  B. J.  (1966) Effects  of  industrial waste on  the  marine environment, J. Water Poll.
    Control Fed.. 38, p 1000.

Ellis, M. M. (1937) U. S. Department of Commerce, Bureau of Fisheries, Bull. 22.

Hem,  J. D.  and Cropper, W. H. (1959)  Survey of ferrous-ferric chemical equilibria  and redox
    potentials, U. S. Geol. Sur. Water Supply Paper 1459A.

Hutchinson, G. E. (1957) A treatise on limnology. Volume I, Wiley and Sons, New York.

Kerr, P. C., et al. (1970) The  interrelation of carbon and phosphorus in regulating heterotrophic
    and autotrophic populations in aquatic ecosystems, FWQA, Southeast Water  Lab, Athens,
    Georgia.

Knentzel, L. E. (1969) Bacteria, carbon  dioxide, and algal blooms, J. Water Poll. Control Fed.,
    Vol. 41, No. 10.

Morgan, J.  J.  and  Stumm,  W.  (1964)  The  role of multivalent metal oxides in limnological
    transformation, as exemplified  by iron and manganese,  Proc. Second  Inter. Conf. on Water
    Poll. Res., Pergamon Press.

Odum, H. T., et al. (1963) Diurnal metabolism, total phosphorus, ohle anomaly and zooplankton
    diversity of abnormal marine ecosystems of Texas, Inst. Texas Mar. Sci.

Pearson, E. A., et al. (1967) Pollution and  marine ecology, Interscience, New York.

Slvey, J. K.  G. and Roach, A. W. (1964) Studies on microbiotic cycles in surface waters, J. Amer.
    Water Works Assoc., p 60.

Thackston, E. L. and Krenkel, P. A.  (1969) Reaeration prediction in natural streams, Proc. Amer.
    Soc. Civil Engineers, Vol. 95, No. SA1.

Wezernak, C. T. and Gannon,  J. J. (1968) Evaluation of nitrification in streams, Proc. Amer. Soc.
    Civil Engineers, Sanitary Engineering  Div.

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        THE  INFLUENCE  OF  TEMPERATURE ON  THE REACTIONS
                    OF THE  ACTIVATED SLUDGE PROCESS
                               Pal Benedek and Peter Farfcas
The  rate of biochemical reactions is  increased by an  increase  in  temperature and vice versa.
However, while the microbial  processes of fermentation  industries are carried out at constant
temperature, biological waste treatment is exposed to temperature changes predetermined by the
prevailing climate. This fact, of course, exerts  an  influence on purification efficiency. Namely,
detention times in the waste treatment facilities are fluctuating in summer and winter between the
same  limits, while the  rate of  the  reaction  - and so the purification  efficiency - decreases
considerably with falling temperature.

Temperature dependence of the biological treatment  process can  be described with a simple
mathematical model only between certain  limits because it is a complex phenomenon. It is well
known that various technological modifications of  the activated sludge process react diversely to
changes in  temperature, the  aerated  lagoons being  most sensitive to the  cold (Table  1).
Explanation of this phenomenon was given by  Eckenfelder (1966) who supposed that the rising
temperature results in anaerobic conditions in the inner part of the floes (oxidation lagoons have
dispersed bacterial systems, whereas activated sludge plants have flocculated ones). Thus, reaction
rate increase with temperature is compensated for in a negative sense by the smaller bacterial mass
taking part in aerobic substrate removal processes.

The situation is further obscured by observations of Wuhrmann (1964), indicating that not only
the rate of the reaction, but also its stoichiometric constants (g O2 consumed/g substrate removed)
are changing with temperature. Downing (1968) pointed out that this was caused predominantly
by the intensive temperature dependence of nitrification. (At temperatures above 10° C nitrogen
metabolism produces NO3, whereas  at lower  temperatures NH^ is formed, the  latter  process
needing  less oxygen.)  It cannot  be  excluded, however,  that the fraction of substrate, being
oxidized for energy yield, is also changing with the temperature.

The aims  of  this study are  to reveal the physico-chemical basis  of temperature dependence
measurements, and based on the kinetic interpretation, to measure the temperature dependence of
individual substrate removal and oxidation processes.

                              KINETIC INTERPRETATION

In a non-steady state system,  the reaction rate,-^ is a function of temperature, T° (in degrees
Kelvin), and reactant concentration. St, at time t, as described below:

                                       ds       n
                                      — = KS"                                    (1)
where^is f(T°, St) and K is f(T°);        *

where  K is the reaction constant (being a function of temperature) and n is the order of reaction.
                                           164

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                                                                                     165
                                       TABLE  1

              Temperature Dependence of Biological Waste Treatment Processes

                           Temperature
        Process               range, C°        Q10           9               Source

Activated sludge                 0 - 20      1.00 -1.48   1.000 -1.040      Eckenfelder, 1966

THckling filter                   0-20         1.41        1.035

Aerated stabilization pond        0-20      1.96-2.15   1.07-1.08

Piper and pulp mill wastes        2 - 30      1.35 -1.56   1.031 -1.046    Carpenter et al., 1968
To describe  temperature dependence of the rate of enzyme-catalyzed biochemical  reactions -
where one cannot speak of an "order of reaction" in the strict physico-chemical sense - Equation 1
modifies to:

                                 dS
                                 -ft = A =  K •  X ' f (St)                               (2)
where both ^ and A are f(T°, St) and K is f (T°);
where x is the concentration of biocatalyst (enzyme or active bacteria)  and f(St) refers to the
substrate dependence of reaction rate, that is, "biological activity", A.

Based on the foregoing generalized  relationships, the Michaetis-Menten  model (Pearson, 1968;
Benedek and Parkas, 1968) can be written:
                                              x-^
where K = Vcmax as f(T°);                           *
                                                         AH
and
                             so K =  Vmax =  (constant) e RT                           (4)

                                               §t
                                    f(SJ  =  -                                    (5)
                                       *    S. + Km
 Equation 4 represents the Arrhenius equation, where AH is the "activation energy" expressed in
 calories  (Thimann, 1964; Johnson, et al., 1957; Ingraham, 1962). Vmax is the maximal value of
 specific  substrate  removal rate defined as-rr" ^j|. Equation 5 is the so called "enzyme kinetic
 function", where Km is the Michaelis constant.

 Supposing that  St < Km (which  is the case under  normal operating conditions in the activated
 sludge process),  the generally known first-order reaction rate can be attained:
                                   yrnax
                              A  =— *X'St = K'-X'St                            (6)
                                    Km

-------
166


where K' is a first-order reaction constant and n = 1.

From the point of view of temperature dependence measurement, it is important that x and f(St)
should be constant. In this case, from Equation 2 it follows that

                                        £l =  Jii
                                        A2    K2

where the  subscripts  1 and 2 refer to A and  respective  K values measured  at two different
temperatures. Metabolic rate  measurements must be made at different temperatures with  the
substrate being removed on the course of a zero order reaction - in this case, reaction rate does not
depend on  substrate concentration,  or St should be the same constant value for all measurements
performed. Of course, sludge  samples have to  be taken from the same system, thus assuring
constant  bacterial concentration (x), too. Adopting the above test conditions, the actual biological
activity  (A), can be measured  instead of the  respective K values, which are difficult to develop.
Metabolic reaction rate parameters  like substrate  and endogenous respiration, substrate removal,
dehydrogenation, etc., are regarded as different forms of A.

To calculate AH from Equation 4 and 7, it follows:

                                        A2            T2 • T,
                             AH = log	 •  2.3 R  •  	                           (8)
                                        A,            T2-T,

As an index for  temperature dependence, the coefficient 6  is  also  used with  the following
definition of Eckenfelder (1966):


                                   —      (T   T )
                                    A! ~                                              *9'

A further symbol characterizing temperature dependence  is  QIC, the factor indicating how many
times the reaction will increase  if the temperature is raised  by 10° C (Thimann, 1964).

                                           A(T° + 10)
                                    Q,o  = 	                                 (10)


An interrelation between the three parameters is given below, and deducted in the Appendix:

                           logQ10  =  10log0  = AH (2.54) (10'5)                       (11)

 For steady state systems, like continuously working activated  sludge plants, hydraulic residence
 time V/q must be employed instead of physical time, t, and S  , effluent substrate concentration,
 instead of St-

The term describing removal activity follows from the materials balance. Equation 2:

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                                                                                      167


where V is  the  aeration compartment volume, q  is the waste flow, and S   is the substrate
concentration in the raw waste. The same rationale is employed as in Equations 2-6, observing the
above indicated changes in t and St,  respectively. Assuming  a first order reaction analogous to
Equation 6. the expression can be written as:



where K' = f (T°),

from which the value of K' can be calculated graphically after rearrangement:


                                    So               V
                                  	= 1 + K'-X	                               (14)
                                    Se               q

and  plotting the  respective  K'  values versus T°,  using either the rearranged Equation  8 or the
logarithmical form of Equation 9, the temperature dependence may be calculated (Carpenter et
al., 1968).

Strictly  speaking, in  Equations  12-14, the  term  Se - Smm,  representing available  substrate
concentration, should be taken for Se, where smm is the so-called "residual BOD" remaining in
the effluent after prolonged biological treatment (Benedek and Farkas, 1968 and Benedek et at.,
1968). If the "residual BOD" is neglected, Sfi will exert  less change in the temperature function
ttian the "available food  concentration",  the  latter having  the  proper direct relationship for
removal rate.

                                     EXPERIMENTAL

Measurements were  performed on endogenous  sludge  that had  been aerated for some days
previously.  Sludge samples were taken from plants treating municipal and pharmaceutical wastes,
respectively. Some tests were also made with sludges grown on pig farm wastes or phenolic wastes.
The temperature range was 0° - 25° C. For a set of measurements, one-liter sludge samples were
taken from  the same  system, chilled  to the desired temperature and thermostatized during the
respiration   or  activity  (substrate  removal)  measurements.  All measurements  were  done  in
non-steady  state (batch fed) systems. Temperature dependence  of the following  processes were
examined:

     Colloid removal rate,

     Oxidation rate of adsorbed colloids,

     Oxidation rate (substrate respiration) of dissolved substrate,

     Endogeneous oxidation (respiration) rate.

In the case  of dissolved  substrate, the amount of O2 consumed  per gram of substrate added was
also determined using the short  term oxygen demand (STOD) process of Vernimmen et al. (1967).

-------
 168

Colloid  removal rate  was measured  mixing a stock colloid substrate solution  (caseine, soap or
starch) with endogenous sludge of about 3 g/l MLSS. It was settled for about 5  minutes, then the
supernatant was filtered and St measured as COD. The SQ concentration for t = 0 was calculated
from the well-known mixing formula.
Removal activity. A, was calculated as follows:

                                          A!
                                    A =	=	                                  (15)
AS    SQ-St
The further fate  of adsorbed substrate was followed by respirometry. Because the biooxidation
rate of starch was found to be very low (substrate respiration could be neglected in comparison to
endogenous respiration), this test was carried out  using a washed caseine suspension. The mixed
liquor containing the  caseine was aerated for an hour after mixing to allow the dissolved fractions
to  oxidize, which was indicated  by an intensive drop in respiration. Respiration rate measured
after the removal of the dissolved fraction was regarded as the net sum of the substrate respiration
due to the biological oxidation of caseine and the endogenous respiration.

Substrate removal  rate  was measured by  means  of the Farkas  (1968) activity  measurement
procedure. Most substrates (acetate, sucrose) were  removed by a zero order reaction, thus assuring
f(SJ to be constant. Substrate load was kept constant for each set of measurements.

 Respiration measurements were  done with  membrane-coated D.O. probes, measuring first the
endogenous respiration at the desired temperature,  then adding a constant amount of the substrate
to be examined  and  measuring the total  respiration. Substrate respiration was calculated as the
difference between total and endogenous respiration.

The log reaction rates (A) were plotted against 1/T°, (see Equation 6), where reactions obeying the
Arrhenius law give straight lines. In all cases where this did not occur, the QIO and 0 values were
calculated for the 0°  C - 10° C and 10° C - 20° C temperature ranges, using Equations 10 and 11.

                                         RESULTS

The rate  of starch  removal - which was a purely adsorptive process - did not show any significant
thermal  dependence. From Figure  1  the AH value was calculated and found  to be 364 calories,
which is much less than AH values encountered in biochemical substrate removal processes.

The plot of the  biochemical oxidation of  adsorbed caseine suspension (Figure 2)  indicates that
biooxidation of caseine obeys the Arrhenius law.

The metabolic rate of dissolved  substrates did not give straight lines in the Arrhenius system, as
can be seen in  Figure 3  in the case of activated sludge grown on municipal waste  and fed acetate.
Nearly the same  result was obtained with the same sludge and sucrose (Fig. 4) and  activated sludge
grown on a pharmaceutical waste, fed phenol and acetate, respectively (Fig. 5).

In  contrast to the above, endogenous oxidation always followed the Arrhenius law. The thermal
dependence of endogenous respiration of four different  kinds of activated sludge is plotted in

-------
                                                                         169
  3,327
  JBSO-
          25       2O
                                                s
                                               —I—
                 3*0
450
460
                                    Reciprocal of ota. iarr^perolurs
FIGURE 1  Temperature dependence of starch removal rate

-------
170
                                                    Terryjerafun? [C.']

                                                    0         S
                                                  Reciprocal of ota temperokjre
                                endogenous                7/  „>]
                                65O rng/i cneese suspension     I <   J
                                32SO mg/i cheese suspension


   FIGURE 2  Temperature dependence of the biological oxidation rate of cheese suspension
Figure 6. Respiration at  20° C was arbitrarily taken as unity to make comparison easier. The
activation energies were within the range of AH = 13,150 ± 550 cal.

All thermal dependence results obtained in this study together with some representative data from
the literature are included in Table 2.

In Figure 7,  the  stoichiometric ratios of substrate oxidation, (g 02/g  substrate)  obtained with
STOD measurements are plotted versus temperature.
For acetate, this ratio seems to remain unaffected by temperature. The value of 0.4 g 02/g acetate
is in good agreement with the results of Warburg's measurements and data of other authors. For
phenol, the stoichiometric ratio ranged from 0.7 to 0.9, the smaller figure being valid at 0° C.

-------
                                                                                171
            437

            f&crian:
            *, Ace/ate load
            2, Activated sludge grown on municipal waste
FIGURE 3  Temperature dependence of the biological oxidation rate of acetate

-------
172
                                                                         500
                     Suu-c&e  load CO mg/i
                   2, Activated  ilrtjp (f-cntn an
         FIGURE 4  Temperature dependence of the biological oxidation rate of sucrose

-------
                                                                                       173
                                               fSedpracal of ate. ierrperature
FIGURE 5   Temperature  dependence of the biological  oxidation  rate of phenol  and acetate,
            respectively

-------
174
                                                    & H• OtOO±S5Ocol
                         Qjgin of activated jMjQQe
                         e  Liquid -sirrte ctng
                         Q  FtarmcLcenticat +phencto: tmstf
                         +-  MurKJpot waste
$ Endajencui
2,MLSS 2-5 gft
                                                      t5-2O
FIGURE 6  Temperature dependence of the endogenous respiration of four different activated
            sludge samples

-------
                                                                                      175
                                      DISCUSSION

The thermal dependence data were in good agreement with those of other authors. Johnson et al.
(1957) statistically analyzed the available body of experimental data comprising a broad variety of
biological processes. They found that two distinct peaks exist in the frequency of occurrence of
AH values:  one between 11,000 - 13,000 cal, (from the results reported herein, the AH values of
dissolved substrates above 10° C - and perhaps, endogenous respiration - belong in this group), the
other  between  15,000  - 18,000  cal, where the  removal of dissolved  substrate  belongs, at
temperatures lower than 5° C.

According to the  Crozier theory, substrate  metabolism cannot  be described with  one simple
Arrhenius equation,  if it is  assumed to be  a complex process comprising a series  of coupled
biochemical reactions.  At different  temperatures  there would be  different  "master reactions"
characterized by different activation energies. (The reaction determining the overall reaction rate is
called "master reaction" by Johnson et al., 1957). The temperature value, where there  is a break
                                        TABLE 2

          Temperature Dependence of The Rate of Metabolism For Activated Sludge
           Metabolism

1.  Adsorptive removal rate of
   starch

2.  Biological oxidation of caseine
   suspension

3.  Removal rate of acetate
4. Substrate respiration with
   acetate

5. Removal rate of sucrose
6. Substrate respiration with
   sucrose

7. Removal rate of phenol

8. Substrate respiration with
   phenol

9. Endogenous respiration
   (4 different sludges)

10. Respiration of activated sludge
11. Rate of nitrification

12. O2 • consumption rate when
    determining BOD
Temperature
  range, C°

    0 -25

    0-25
AH
cal
364
Q10 . 6
1.022 1.000
Source
Fig. 1
17.000   2.66   1.103
Fig. 2
0
10
0
10
0
10
0
10
0
10
0
10

0
0

-10
-25
-10
-25
-10
-20
-10
-20
-10
-20
-10
-20
-
-20
-25
.
7.200
33.700
7.200
37.000
.
-
_
-
.
-
.
1
.51
6.90
1
8
5
2
6
2
3
1
3
.51
.42
.80
.86
.50
.72
.87
.72
.18
2.0
13.150

-

2
2
2
3
.15
.25
.04
.81
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
.042
.214
.042
.242
.192
.110
.206
.105
.131
.056
.134
.072
.078
.085
.074
.143
Fig.
Fig.
Fig.
Fig.
Fig.
Fig.
Fig.
Fig.
Fig.
Fig.
Fig.
Fig.
Fig.
3
3
3
3
4
4
4
4
5
5
5
5
6
Eckenfelder
Wuhrmann,













,1966
1964
Downing, 1968
    4 -20
   20 -30
         3.55   1.135   Eckenfelder, 1966
         1.72   1.056   Eckenfelder, 1966

-------
176
                             • ptenoi

                             x acetate
                     Ifl
                     OS
                    x
                                                 «
                                                 •
                                                 •
1 iamb, et at'.[e]
                                                                   Onto
         FIGURE 7  Temperature dependence of substrate oxidation oxygen demand
on  the  Arrhenius plot, is called  the  "critical temperature", where two  master reactions are
supposed to "switch over." In  Figure 3, a sharp break at 7° C can be observed on the Arrhenius
plots of both acetate removal and substrate respiration, and with all dissolved substrates, a more or
less pronounced "bend" can be seen in the range of 5° C - 10° C.

It is known  that dehydrogenases have AH values of 1 1,200 calories, and cytochromes (respiration
enzymes underlying cyanide poisoning) have AH = 16,000, but the data is too fragmentary to
conclude  that  above  10°  C  the  master  reaction   is  dehydrogenation,  and  at  0°  C,
cytochrome-catalized respiration.

The Arrhenius  plot  of  the metabolic  reactions of activated   sludge  is  similar  to  those  of
psychrophylic  bacteria that exert a technologically utilizable metabolic activity even at  0°  C
(Ingraham, 1962).

Strikingly, the biooxidation of adsorbed food readily follows the Arrhenius law. According to
present knowledge, adsorbed food must be hydrolyzed and transformed into dissolved compounds
prior to biological utilization. Considering this, it remains an open  question why caseine oxidation
shows a temperature dependence different from the dissolved substrates.

Endogenous respiration also does  not show any "critical  temperature value." It seems plausible
that endogenous metabolism has only one master reaction in the 0° C * 25° C temperature range.
Endogenous "basic"  metabolism has to be very stable because it is more important from  the point
of  view  of survival  and resistance against adverse environmental  conditions  than  substrate
metabolism. It may be assumed  that  endogenous metabolism, as a well-stabilized biochemical
reaction chain, has only one "master reaction", consequently behaving as one simple reaction.

-------
                                                                                     177


The amount of substrate oxygen demand changes little with temperature. This is in fair agreement
with the findings of others (Vernimmen et al., 1967 and Lamb et al., 1964} (Fig. 7). This means
that in the instances  studied only  the reaction rate, but not its stoichiometric constants, has
changed with the temperature. Similar  conclusions were drawn from  BOD curves recorded at
different temperatures (Gotaas, 1948; Wilderer et al., 1969; Chia, 1969).

Final conclusions concerning thermal  dependence  of the activated sludge process can be drawn
only from the continuous process. The  calculation of  K;, according to Equation  12, is possible
only if a large collection of data is at hand. The S /Se ratio usually has a  great fluctuation, and the
data must be treated statistically (Wuhrmann, 1964).

                                     CONCLUSIONS

    1.   Endogenous metabolism follows the Arrhenius law, while the metabolism of dissolved
substrate does not. An explanation to  this  is sought  in the Crozier theory, supposing that at
different temperatures,  different master  reactions (having different activation energies) are the
"bottlenecks" of the biological reactions.

    2.   The adsorptive mechanism of activated sludge also has a  temperature dependence, but
this amounts to less than 10% of the thermal dependence of biological processes.

    3.   The value of grams-oxygen consumed per gram substrate oxidized was found practically
constant in the range of 0° - 25° C.

    4.   Temperature dependence of continuously working activated sludge plants is usually less
than would be expected from non-steady state measurements. From the possible explanations of
this phenomenon, the Eckenfelder theory of partial anaerobiosis  within the floes was mentioned.
Further, it should be  kept in mind that most wastes contain colloids, the removal rate  of which
does not  depend  on  temperature. A great  difference  may be  encountered in the  thermal
dependence of treatment efficiency, depending on whether the waste contains colloids or dissolved
compounds, in favor of the former.

    5.   A great importance has  to be attributed to heat storage  in water bodies underlying
biological treatment; a system with long detention time may not be economic, because the thermal
reserve - consequently, higher removal rate - of a short detention time system may compensate for
the long detention time with heat loss in a total oxidation plant.

                                       APPENDIX

Interdependence Between The Thermal Coefficients of AH, 0, and Q, 0

From the Arrhenius equation. Equation 4, it can be written:

                                    A2     AH    T2 - T,
                                log—  =  —   ' 	                            (A-1)
                                    A,    2.3 R   T2 ' T,

-------
178


From the above equation, R = 1.99 Kcal/mol.K°, and T2 ' Tt has the approximative value of
85,850 in the temperature range of 0° C - 30° C. Thus it can be written:

                      A2      AH       T2-Ti     AH
                  log	=    	   '	 =   	   -(T2-T!)              (A-2)
                      A!   (2.3)(1.99)   85,850   394,910

Introducing the 6 constant:

                                    AH
                           logfl =  	   = AH <2.54)(10'6)                       (A-3>
                                   394,910
From A-2 and A-3 we obtain:
                                    A2
                                log	 =  log0(T2 -T,)
or
                                    A2
                                   	 = 0 
-------
                                                                                   179


Chi a Shun Shih and Stack, V. T., Jr. (1969) Temperature Effects in Energy Oxygen Requirements
    in Biological Oxidation, J. Wat. Pollut. Control Fed., 41, R461.

Downing, A. (1968) Factors to be  Considered in the Design of Activated Sludge Plants, Advances
    in Water Quality Improvement, Univ. of Texas Press, Austin.

Eckenfelder, W.  W., Jr. (1966) Industrial Water Pollution Control, McGraw Hill Book Co., New
    York.

Farkas,  P. (1968) Method for Measuring Aerobic Decomposition Activity of Activated Sludge in
    an  Open System,  Fourth Conf on Water Pollution Research, Pergamon  Press, London (In
    press).

Gotaas, H. B. (1948)  Effects of Temperature  on Biochemical  Oxidation of Sewage, Sew. Wks.
    Jour.. 20, 441.

Ingraham, J. (1962) Temperature Relationships, The Bacteria, IV, Academic Press, New York.

Johnson, F.  H., Eyring, H. and Polissar, M. J. (1957) The Kinetic Basis of Molecular Biology, John
    Wiley and Sons, New York.

Lamb, J. E.,  Westgarth, W. C., Rogers, J. C. and Vernimmen, A. P. (1964) A Technique for
    Evaluating the Biological Treatability of Industrial Wastes, J. Wat. Pollut. Control Fed., 36,
    1263.

Pearson, E. A. (1968) Kinetics of Biological Treatment, Advances in Water Quality Improvement,
    Univ. of Texas Press, Austin.

Thimann,   K.   W.   (1964)   Das   Leben  der  Bakterien  Wachstum,  Stoffwechsel  und
    Verwandtschaftsbeziehungen, Fischer, Jena.

Vernimmen, A. P., Henken, E. R. and Lamb, J.  C. (1967) A  Short-Term Biochemical Oxygen
    Demand Test, J. Wat. Pollut. Control Fed., 39, 1006.

Wilderer,  P.,  Hartmann, L. and Janeckova, J. (1969)  Der  Einfluss der Temperatur auf dem
    BSD-Endwert, Vortrag., Universitat, Karlsruhe.

Wuhrmann,  K. (1964)  Hauptwirkungen und  Wechselwirkungen  einiger  Betriebsparameter  im
    Belebtschlammsystem. Ergebnisse mehrjahriger Grossversuche EAWAG, Vertrag, Zurich.

-------
                  TEMPERATURE  EFFECTS ON  BIOLOGICAL
                        WASTE TREATMENT  PROCESSES
                        W. Wesley Eckenfelder. Jr. and A. J. Englande
                                    INTRODUCTION

Variations in  liquid temperature affect biological waste treatment processes in two interdependent
ways. First, the  oxygen utilization  rate which reflects the energy transfer  of the process has a
defined  temperature  relationship.  This reaction-temperature  dependency is  reflected  by  a
temperature coefficient 0. Secondly, in any biological system a relationship will exist between the
oxygen transfer rate to the biomass and the oxygen utilization rate of the biomass. It is therefore
necessary that 6  also consider the effect of temperature on the oxygen transfer rate. The absolute
temperature effect on the performance of a particular process will therefore be the  resultant of
these two effects.

In  order  to  estimate  the  thermal  influence  on  a process,  a modification of  the  Van't
Hoff-Arrhenius equation is usually used:
                                      K=  K   o  fi (T-20)
                                    T     20 C
 It should be noted that this relationship  is valid only within specific limits. A lower limit is
 imposed by  retardation of  bacterial activity  for  mesophilic  organisms as the temperature
 approaches freezing. Relatively high reaction rates may still exist  at very low temperatures for
 psychrophilic organisms The rate of the biological reaction rates will increase in accordance with
 Equation 1 with temperature to an  optimum value for most aerobic systems. Further increases in
 temperature result  in a decreased  rate for mesophilic organisms.  Maximum  biodegradation by
 thermophilic organisms, however, will be obtained over a temperature range of 35° C to 65° C.

 The effect of temperature on biological processes is the resultant of several factors which consider
 the type and distribution of microorganisms, the type of process and the design and operation of
 the system.

 Bacteria can be broadly classified into three categories as to their response to temperature, namely
 psychrophilic, mesaphtlic and thermophilic. Each of these categories have an effective temperature
 range.  By  far,  the majority of wastewater treatment processes function in the mesophilic range,
 although it has been demonstrated that some processes  in  northern  climates function in  the
 psychrophilic range. A few systems have been designed  and operated in the thermophilic range.
 Probably,  the most responsive factor relating temperature effect to  process performance  is  the
 food/microorganism ratio (F/M). At high F/M values the  biomass may be filamentous or dispersed
 and 6 will be high  indicating a direct temperature effect on each organism. By contrast, at lower
 F/M ratios the biomass is flocculated and diffusional mechanisms into the floe become significant.
 More of the  floe  is  aerobic  at lower temperatures  so that a greater aerobic biomass  at  lower
 temperatures is capable of stabilizing almost the same quantity of organic matter as a smaller more
 active  biomass at higher temperatures. It is because of  this that the activated sludge process at
 conventional loadings (F/M 0.6) and trickling filters yield  a much lower temperature coefficient, 8,


                                           180

-------
                                                                                     181
than those processes using primarily dispersed growths such as the aerated lagoon. It is probable
that the mixing intensity in the process which affects floe dispersion also influences the coefficient
0. Temperature effect on the various processes are shown in  Figure 1.

In  order to adequately  predict the  magnitude  of  the  temperature influence on a system's
efficiency, an  appropriate 8  value must be employed. The  temperature  coefficient will vary
depending primarily on the nature of the process under consideration. This paper discusses 6 for
various  biological process relationships.  The  processes considered include  waste  stabilization
ponds, aerated  lagoons, and activated sludge.
    I.O
                                           AERATED LAGOONS AND
                                                      STABILIZATION BASINS
        EXTENDED
          AERATION
 ACTIVATED SLUDGE
        DISPERSED
              FLOC
FLOCCULATION
FILAMENTOUS AND DISPERSED GROWTH
                    RANGE RELATED TO
                           MIXING INTENSITY
                                          F/M
 FIGURE 1  Relationship between temperature coefficient, 8, and food to microorganism ratio,
            F/M
                                DETERMINATION  OF  0

The temperature influence  on a waste treatment process is usually reported  as a change in the
percent removal of BOD. The temperature coefficient 8 which reflects the change  in reaction rate
can be computed by graphical methods. Alternative calculations may be employed depending on
the type of data available and the type of process used.

Figure 2 illustrates one method of  analysis which is developed as follows for completely mixed
aeration systems:
The BOD removal relationship can be defined as

-------
182
                                     VSe
                                                                                      (2)
in which
    S  and S  are the influent and effluent BOD concentrations respectively
     O     c


    X is the aeration volatile solids concentration



    t is the aeration time



    k is the mean reaction rate coefficient
and
                                 VSe
                                        = % removal (R)
                              (3)
Combining Equations 2 and 3 one obtains:
                                            =
                                      1 -R
                                                                                      (4)
             2.0
               1.0


           >•  .8




               .6
                                     I
_L
                           10        20        30        40

                                        TEMPERATURE (°C)
          50
60
           FIGURE 2   Temperature function for activated sludge (Hunter et al., 1967)

-------
                                                                                     183

Let the left side of Equation 4 equal Y. Then, if Xv and t remain constant, kj is proportional to
                                    T Ort
One can rewrite the equation k  =     ®     m tne f°rm
                                     Y =  G  ' 01"-20                                   (5)
where G is a constant;

thus
                               log Y  = log G + (T-20) log 0                             (6)
As shown in  Figure 2, 6  is computed from the slope of a semilog plot of Y versus temperature for
a constant t and Xy.

The temperature coefficient for aerated lagoons where the detention time varies can be computed
from Equation  1:

                             logkT  = Iogk20 + (T-20)log0                          (1a)

A semilog plot  of percent BOD remaining versus detention time will yield a slope representative of
the reaction rate k. In accordance with Equation 1a, a plot of k versus temperature (as shown in
Figure 4) will yield the coefficient &.

Values for the  reaction rates may also  be obtained by direct calculation using Equation 2, and the
coefficient & computed.

                            WASTE  STABILIZATION  PONDS

Temperature  has   a significant  influence  on   waste  stabilization  pond  efficiency.   Both
photosynthetic oxygen  production  and  biological degradation  rates  are greatly  affected  by
temperature  variations.  While optimum  photosynthetic activity is maintained at approximately
20° C, the upper and lower limits appear to be about 35° C and 3° C respectively.

A  value for  8  of  1.072 was obtained by  Herman and Gloyna  (1958) for a temperature range
between 3° C and  35° C. Suwannakarn and Gloyna (1964) found 9 equal to 1.085 for a synthetic
soluble sewage  between 9° C and 35°  C. Oswald (1966) found a temperature coefficient of 1.075
for domestic sewage between temperature limits of  10° C and 18° C. All the reported values are in
dose agreement, providing an average 8 value of 1.077.
                                 ACTIVATED  SLUDGE

Table 1 summarizes 8  values computed from data available in the literature for activated sludge
processes. Temperature coefficients range from  1.0 to 1.041. The value of 1.076 computed from
Vfahrmann  (1966)  is  the probable  result  of a  dispersed  growth  due  to  the very  high
]food-rnicroorganism ratio of 2.03.  Data reported by Hunter et al. (1967) are shown in Figure 2. A
value of 6 was determined  to be 1.035 for the synthetic sewage over a temperature range of 4° C

-------
           TABLE  1
Temperature Coefficient Evaluation
        Activated Sludge
Temp.
Range
C
4-45
5-30


26-37
9-17


10-25
F/M**
0.58
0.44
0.81
0.45
0.57
2.03
0.43
0.22
0.74
MLVSS
(mg/1)
1,600*
1,100
1,100
1,870
3,200*
480*
2,640*
4,800*
800*
A,
623
435
435
750
229
108
124
115
248
Substrate
Synthetic Sewage
(dry dog food meal)
Slurried dog
food meal
Dog food meal
witn dextrose
& gelatin
Phenol
Kraft black
liquor
Domestic Sewage


Domestic Sewage
Batch or Detention
Continuous Time (hr)
Batch
(bench scale)
Continuous
(bench scale)


Continuous
(bench scale)
Continuous
(pilot plant)


Batch
(bench scale)
16
12


3
2.67


10
                                                    6            Source
                                                  1.035   Hunter et al. (1967)

                                                  1.037   Ludzack et al. (1961)

                                                  1.041

                                                  1.016
                                                   1.006   Carpenter et al. (1968)

                                                  1.076   Wuhrmann (1966)

                                                  1.0
                                                  1.0
                                                   1.015   Sawyer (1940)

-------
                                                                                      185


   to 45° C. Further increases in temperature resulted in a sharp decrease in process efficiency. This
   data could be interpreted to show a detrimental effect of temperature below 20° C and above 45°
   C. A lower optimal temperature was found  by  Carpenter et al. (1968) as 37° C. An activated
   sludge plant at a West  Virginia Pulp and Paper Company  plant showed  a decrease in process
   efficiency at temperatures in excess of 40° C. The activated  sludge process appeared to function
   satisfactorily at temperatures as low as 4° C.
                                          TABLE 2

                              Temperature Coefficient Evaluation

                                       Aerated Lagoons
Temp.
Binge MLVSS
°C F/M (mg/1)
10-30 -
13-20 2.51 106*
2-30 2.50 80*







S
(mgTl) Substrate
Cotton Textile
Waste
266 Domestic Sewage
200 Kraft
Neutral sulfite
semichemical
Acid sulfite
Roofing felt
Board mill
Avg. of all 5
<10°C
>10°C
Batch or
Continuous
Continuous
(pilot plant)
Continuous
Continuous
for 2.5 & 5
day detention

Batch

(bench scale)



Detention
Time (days) 6
2.6-5 1.035
8.6 1.046
2.5-10 1.031
1.046
10 1.039
1.040
1.031
1.035
1.058
1.026
Reference
Sawyer (1940)
Eckenfelder (1971)
Carpenter et al. (1968)







* Assumed MLSS = 50% influent BOD

Assumed MLVSS = 80% MLSS
                                   AERATED  LAGOONS

  Pertinent descrtptives and computed temperature coefficients for the aerated lagoon process are
  summarized in Table 2. A range of 9 from 1.026 through 1.058 was observed.

  Hie variation  in BOD removal characteristics over a temperature range of 10° C - 30° C from
  continuous treatment studies by Sawyer (1966) is shown in Figure 3. The temperature coefficient
  from these data is 1.035.

-------
186
                                           345
                                         DETENTION, days
             FIGURE 3   Temperature function for aerated lagoon (Sawyer, 1966)
Carpenter et al. (1968) conducted an extensive study of pulp and paper mill wastes and calculated
an average 0 of 1.035 for five different wastes over a temperature range of 2° C - 30° C. Figure 4
shows the graphical solution for 9. It is significant to note that two temperature coefficients might
better describe the presented data than the one  reported. The same trend was observed for  each
waste indicating a 0 equal to 1.026 and 1.058 for temperature limits  of  10°  C  - 30° C and 2° C -
 10° C respectively.

 Sawyer (1966) and Carpenter  et al. (1968) conclude that  aerated lagoons with  short detention
 times will be  extremely sensitive  to temperature change. This effect is  dampened by retention
 periods in excess of five days.

 There have been recent reports of a relatively small temperature effect on aerated  lagoons treating
 domestic sewage in northern climates. Two factors must be  considered in interpreting such data.
 Rrst, the major portion of the BOO in domestic sewage is present in suspended and colloidal form
 and a primary removal mechanism is adsorption and flocculation. These mechanisms are relatively
 insensitive to  change  in temperature.  Secondly,  the  retention periods  in most aerated  sewage
 lagoons are  long  and changes in  removal  due to temperature  are wasted.  It is  the  writer's
 contention that further studies on temperature effects of these systems are  needed before  valid
 conclusions can be drawn.

-------
                                                                 187
  0.7
  0.6 -
  0.5
  0.4
 >
o>
   0.3
  0.2
                  6=1.026
                                        REPORTED VALUE
                               	  PROPOSED VALUES
                  J_
                               20          3O
                          TEMPERATURE (°C)
     0            10


FIGURE 4   Derivation of temperature coefficient for aerated lagoon
4O

-------
188
                                       DISCUSSION

The  summary presented  in Table 3 indicates  the appropriate 0 and corresponding temperature
range for the various aerobic biological processes employed in wastewater treatment. Variations in
the temperature coefficient can be  rationalized by considering the inherent difference in process
operation.

The  parameter most  influential in determining process temperature sensitivity  is the food  to
microorganism  ratio (F/M).  The characteristics of the biomass will be dictated in  major part by
F/M. At very high values of F/M the biomass  is dispersed. At intermediate organic loading  levels
dispersed filamentous growths may  develop. At low loading levels, flocculation occurs, resulting in
the formation of gelatinous floes containing millions of individual organisms. Under starvation
conditions floe dispersion will result. In the activated sludge process an  F/M ratio approximately
equal to 0.5 results in a flocculated biological  growth. BOD  removal and oxidation are obviously
affected by such growth. The amount  of oxidation depends  on diffusion of oxygen  into the
biological  floe, where it  is subsequently utilized by the  microorganisms. At conventional mixing
intensities, relatively large floes are  generated.  The portion of these floes that are aerobic depends
upon a balance between oxygen diffusion into the floe from the surrounding  liquid and the
oxygen consumption  by  the  organisms  contained  within the  floe. At low temperature, a low
oxygen utilization rate permits diffusion  of oxygen  to a greater depth in the floe and therefore a
large portion of the floe is aerobic. At high temperatures, the increased respiration rate depletes
the oxygen rapidly, and only a small portion of the floe is aerobic. It can  be postulated that a large
mass of organisms at a low respiration rate (winter) achieves the same degree of oxidation as a
small mass at a high respiration rate  (summer),  and hence the computed coefficient 6 may be close
to 1.0. At high mixing intensities in the aeration basin, the smaller floe sizes may be fully aerobic
under all temperature  conditions and the coefficient 8  will  increase. At  the  higher F/M ratios,
filamentous or dispersed growths  will  exhibit a high  temperature dependency as  shown by
Wuhrmann (1966).
Process

Stabilization Pond
Activated Sludge
Aerated Lagoon
Trickling Filter
Aerobic - Facultative Lagoon
Anaerobic Lagoon
Extended Aeration

* This paper
                                         TABLE 3
                                      Summary Table
  9 Range

1.072 - 1.085
 1.0 -1.041
1.026-1.058
   1.035
 1.06-1.18
 1.08 -1.10
   1.037
Temperature
 Range ° C

   3 -35
   4 -45
   2-30
   10-35
   4 -30
   5-30
   10-30
    Reference
 Rowland (1958)
Eckenfelder (1970)
Dietzetal. (1966)
National Sanitation
Foundation (1966)

-------
                                                                                      189


It would therefore appear that the effect of temperature on the activated sludge process is related
both to the loading level (F/M) and to the intensity of mixing in the process. Trickling filters are
analogous to activated sludge except that oxygen diffusion into the film is uniplaner which results
in a 6 value in the order of 1.035.

Waste  stabilization ponds,  aerated and aerobic-facultative  lagoon  and  anaerobic  pond processes
operate at lower solids levels and/or higher F/M. Recent data have shown that the  biomass does
not effectively flocculate at concentration levels below approximately 500 mg/l. Therefore, within
tfiese  systems,  the biomass  is dispersed  and  hence the  process is more directly  affected by
variations in temperature.

High   solids  concentrations  and  long  retention   periods  contribute   to  a low  F/M   ratio
(approximately 0.12)  and a dispersed floe in the  extended aeration process. The value of & would
therefore be expected to be higher than that for conventional activated sludge.

The results for various processes are summarized in Table 3.
                                     CONCLUSIONS

1.  The effect of temperature upon process efficiency can be formulated in terms of a temperature
coefficient, 6. 6 can be obtained graphically by variations of the modified Van't Hoff-Arrhenius
equation.

2.  Temperature effects  are  minimal on  activated sludge  process performance as compared  to
other treatment systems. The low sensitivity of the activated sludge process is primarily due to the
F/M ratio which results in a flocculated biological growth.

3.  There is some evidence that 6 will increase at temperatures less than 10° C.
                                      REFERENCES

Carpenter, W. L, Vamvakias, J. G. and Gellman, I. (1968) Temperature Relationships in Aerobic
    Treatment and Disposal of Pulp and Paper Wastes, J. Wat. Pollut. Control Fed., 40, 783.

Hermann, E. R. and Gloyna, E. F. (1958) Waste Stabilization Ponds, III,  Formulation  of Design
    Equations, Sewage Ind. Wastes, 30,963.

Hunter, J. V., Gentefli,  E. J.  and Gilwood, M.  E.  (1967) Temperature and  Retention  Time
    Relationships in the Activated Sludge Process, Proc. 21st Purdue Ind. Waste Conf., 121, 953.

Oswald, W.  J. (1966) Advances in Anaerobic Pond Systems Design, Advances in Water Quality
    Improvement, Univ. of Texas Press, Austin.

Sawyer, C. N. (1966) New Concepts in Aerated  Lagoon Design and Operation. Advances in Water
    Quality Improvement, Univ. of Texas Press,  Austin.

-------
 190


Suwannakarn, V. and Gloyna, E, F. (1964) Efect de la Temperature en el Tratamiento de Aquas
     Residuales Mediante Estanques de Estabilizacion, Vol. de la Off. Sanitaria Panamericana,
     World Health Org., 43,128.

Wuhrmann, K.  (1966)  Research Developments in  Regard to Concept and Base Values of the
     Activated Sludge System, Advances in Water Quality Improvement, Univ. of Texas  Press,
     Austin.

-------
  EVALUATION  OF AERATED LAGOONS  AS A SEWAGE TREATMENT
            FACILITY  IN  THE CANADIAN PRAIRIE PROVINCES
                             Archie R. Pick, George E. Burns,
                          Dick W. Van Es and Richard M. Girling
                                   INTRODUCTION

Metropolitan Winnipeg has a population of 500,000 and is located at latitude 49° 45' N, longitude
97° 15' W. The climate is of the continental type, with an annual temperature of 36.50° F, the
coldest month is January with  an average temperature of  -20° F.the warmest month is July with
an average temperature of 67°  F above, and the average frost-free period (32° F) is 115 days. The
average winter snowfall is 51  inches.

In 1967, the Metropolitan Corporation of Greater Winnipeg undertook a two-year study of aerated
lagoons,  because  there was  little  documented  information  on aerated lagoons operating under
Canadian  prairie conditions.  In  order to assess the applicability of this process for the treatment of
domestic  wastes,  three  pilot aerobic-anaerobic  aerated  lagoons were  constructed by  the
Corporation.

During the summer and fall of 1967 the pilot lagoons were constructed in the corner of an existing
stabilization pond. The sewage treated  was domestic  sewage from  a separate system. The three
aeration systems installed were:

    Air-Aqua*
    Mechanical Surface Aerator**
    Air-Gun***

The work was supported by  Public Health Research Grant 606-7-167 of the  Department of
National Health and Welfare, Canada.

                       DESCRIPTION OF THE PILOT LAGOONS

Each system was designed to treat a flow of 0.5 Imgd. The general arrangement of the systems is
shown on Figure 1 and the design data is summarized in Table 1.

Air-Aqua

This  system operates on  the diffused  air principle.  A  30-HP  compressor supplies air  to
polyethylene tubes laid in a tapered grid on the cell bottom. The system has a 30-day retention
time, an operating depth  of  10 feet and is divided into two  cells, operating in series. 10% of the
effluent is returned to the inlet  for seed.

*   As manufactured by Hinde Manufacturing Limited, Hamilton, Ontario.
** Equipped with Lightnin  Aerators as manufactured by Greey Mixing Equipment Limited,
    Toronto, Ontario.
*** As manufactured by Aero-Hydraulics Corporation, Montreal, P.Q.

                                          191

-------
192
                                                                MOTE
                                                                    ALL DIMENSIONS TAKEN
                                                                    AT BASIN FLOOR
                              •I'-IO"
                                               SURFACE AERATOR
                             FIGURE 1   Plan of the aerated lagoons

-------
                                                                                                 193
                                        TABLE 1
                                 Summary of Design Data
                Item

Average Design Flow

Influent 5-day BOD 20° C

Influent Suspended Solids

BOD Removal rate Coefficient (Base 10)
 k, atO  C

BOD Removal rate Coefficient (Base 10)
 kj at 20 C

Temperature Coefficient 8 (applied to k]

Oxygen Utilization factor a (Ibs.
 oxygen required per Ib. 5Tday
 BOD removed)

Oxygen transfer ratio (ratio of O2
 transfer to waste to that  of water)
 (a factor)

Saturation value of waste  compared to
 H2 O ((3 factor)

Solubility of oxygen 20° C (780')

Operating dissolved oxygen

Effluent Temperature - winter
Effluent Temperature - summer

Influent Temperature - winter
Influent Temperature - summer

Mean ambient air temperature - winter
Mean ambient air temperature - summer

Treatment efficiency required

Retention time - Air-Aqua
Retention time - Surface Aerator
Retention time - Air Gun

Operating depth - Air-Aqua
Operating depth - Surface  Aerator
Operating depth - Air-Gun

Volume - Air-Aqua
Volume - Surface Aerator
Volume - Air-Gun

Mixing requirements for surface aerators

Process loading - a) Design
Process loading -   - Air-Aqua
Process loading -   - Surface Aerator
Process loading -   - Air-Gun

Process loading -b) Actual
Process loading -   - Air-Aqua
Process loading -   - Surface Aerator
Process loading -   - Air-Gun

Design Formulation:
                                    Value and Units

                                    0.5 Imgd

                                    250 mg/1

                                    180mg/l


                                    0.13 per day


                                    0.50 per day

                                     1.072 per ° C



                                    1.50



                                    0.85


                                    0.95

                                    9.02 mg/1

                                    2.00 mg/1

                                    32° F
                                    75° F

                                    48° F
                                    65° F

                                    -16°F
                                    +75° F

                                    90%

                                    30 days
                                    20 days
                                    20 days

                                    10ft.
                                    lift.
                                    17ft.

                                    15 x 10* gal.
                                    10 x 10° gal.
                                    10 x 10° gal.

                                    0.016 HP/1000 gals.


                                    0.52 Ibs. BODs/1000 ft3/day
                                    0.78 Ibs. BODj/1000 ft3, /day
                                    0.78 Ibs. BODS /1000 ft3 /day


                                    0.37 Ibs. BODj/lOOO ft3/day
                                    0.55 Ibs BOD5/1000 ftyday
                                    0.55 fbs. BODS/1000 ft*/day
                                       2.3kj (100 -E)
Ibs. O2 per day  =
                                                  = a' Ibs. BODS removed/day

-------
 194

Surface Aerator

This system consists of eight 20-HP aerators installed in series along the lagoon basin. The basin is
sized for a 20-day retention time and has an operating depth of 11 feet. The raw sewage is fed in
adjacent to the first aerator only.

Air-Gun

A combination of the diffused air and surface aerator principles is used for this system. There are
54 guns installed in a tapered grid pattern. A 40-HP compressor delivers air into an inverted siphon
in the gun base, where a large bubble is formed which rises inside the gun, pushing water ahead and
exploding at the surface. The system has a 20-day retention time and  an operating depth of 17
feet.
                                        RESULTS

 Effluent Quality

 The raw sewage concentration for the period January 1, 1968 to September 30, 1969 averaged
 175 mg/l and 188 mg/l for BODS and SS respectively. Corresponding effluent quality for the same
 21 month period was:

                                        BOD rag/1                               S.S. mg/l

 Air-Aqua                                   37                                      34
 Surface Aerator                            38                                      39
 Air-Gun                                    34                                      34
Figures 2 and 3 show these in detail.

The effect of cold weather on BOD5 removal is evident when the winter of 1968-69 is compared
to the summer of 1968 on Figure 2. The loss of efficiency during the summer of 1969 is attributed
to sludge which will be discussed below.

The results were analyzed statistically for the 12 month period September 30, 1968 to September
30, 1969 (See Fig. 4 & 5).  This period was selected as the most typical for continuous operation.

The median value of the  effluent BOD for the three systems ranged between 39 and 38 mg/l. On
10% of the occasions the effluent was greater than or equal to 78 mg/l.

Suspended Solids removal  remained reasonably  constant  over the 21-month period, with  the
exception of start-up, which can be attributed to initial erosion and suspension of materials from
construction. On the 12-month basis the median SS in the effluent ranged between 21 and 23 mg/l
and on 10% of the occasions greater than or equal to 48 mg/l.

Figures 6 and 7 illustrate results for temperature and D.O. respectively.

-------
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-------
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-------
                                                                                     197
Nutrients
Figures 8 and 9 show the average performance of the aeration systems in the treatment of algal
nutrients, phosphorus and nitrogen. The average percent removals over the test period were:

System                                                 Nutrient Removal
                                    Total Nitrogen (N)                     Phosphate (PO4)

Air-Aqua                                 12.6%                                16.9%
Surface Aerator                           14.6%                                19.5%
Air-Gun                                  10.0%                                23.3%

Although there was  a  reduction of total phosphorus through  all systems, the orthophosphate
concentrations in the effluent increased. The nutrient removal  efficiencies  were  relatively low
compared to  results on  ponds reported by others (Azzenso and  Reid, 1966). The conventional
activated sludge plant operated by the Corporation has removal rates of 36% and 45% for nitrogen
and phosphate respectively. There was no appreciable difference in removal rates between summer
and winter.

The aeration systems are basically equal in nutrient removal and are relatively ineffective.

Temperature

The  effluent  temperature follows the  ambient  temperature  curve  closely  as  it is almost
independent of the raw sewage temperature (Fig. 6). There is a four-month period during the year
when the effluent temperature  is between 0° C and 1° C.

One  of the  concerns in design  was the possible freezing of the Air-Gun cell, as little information
was available  on  heat loss  through ice cover. To keep the heat loss at a minimum, the surface area
was reduced by making the side  slopes steeper. Observations proved, however, that the cell had a
built-in self-protection system. When the temperature rose to 10° F the ice melted  on 25% of the
cell, but as soon as the temperature dropped the cell covered with ice to conserve heat.

                               SLUDGE ACCUMULATION

The three aeration systems have  shown a substantial build-up of bottom sludges. Samplings were
conducted during July 1968, in the fall of 1969 and early in  1970. The accumulation of  sludge  in
aerated lagoons has been recognized by others (Thimsen, 1965; Barnhart, 1965; Clark and Dostal,
1968); however, the significance  of the accumulation of sludge deposits under climatic conditions
similar to those experienced in  the Canadian prairies has not been reported.

The rate of sludge accumulation  in the Air-Aqua system has  been estimated to be approximately
0.18 to  0.25 Ibs. of dry solids per capita per day (based on  population equivalents). The  rate is
comparable to the 0.21 Ibs. of dry solids per capita per day  pumped to digestion at an activated
sludge plant operation by the Corporation.

Theoretical Sludge Accumulation

Theoretically,  the overall  digestion rate is sufficient to reduce  the  amount of volatile  sludge
accumulated to a relatively stable content each summer. After the first summer of operation an

-------
 198
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       01   06   2  5  I  2 345   10 15 20 30 40506070 608590  9596979699   998 9 96 9999

                         PERCENT OF TIME EFFLUENT LESS  THAN
         FIGURE 4   Variability of final effluent BODS (Test lagoons on a one year basis)


annual cycle should occur with the sludge accumulation reaching a maximum in March-April and
decreasing to a minimum level in August-September. The theoretical  cycle is shown in Figure 10
(based on temperature-corrected anaerobic digestion rates).

Based on the accumulation of all suspended solids removed, and 0.45 pounds of solids synthesized
per pound of BODS  removed, the daily sludge production would be  1,120  pounds. If the end
products of anaerobic digestion had been removed from the systems, the amount of accumulation
at the September 1969 sampling would  have been an estimated 200,000 pounds (average daily
accumulation of approximately 300 pounds).
Observed Sludge Accumulation

Based on actual surveys, the sludge accumulation (as  dry  solids)  to September 5, 1969 was
estimated as follows:
Air-Aqua Primary
Air Aqua Secondary
Air-Gun
Total Lbs.

 740,000
 145,000
 580,000
Lbs/day

 1,120
  220
  930
Lbs/0/day

   0.21
   0.04
   0.18

-------
                                                                                     199
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   FIGURE 5  Variability of final effluent suspended solids (Test lagoons on a one year basis)

Sampling of the Air Gun had to be done through 15 feet of supernatant  liquor and these figures
are subject to confirmation. Only  two samples were obtained in the Air-Aqua secondary, so the
reliability  of the 145,000 pound estimate is  poor. Considering the methods of obtaining data, it
was concluded  that  there was no apparent difference in the quantities  of  sludge between  the
systems, the significant point being that the accumulation was considerably greater than expected.
An analysis of the sludge from the Air-Aqua system indicated a moisture  content of 90% for the
primary cell and 92% for the  secondary cell; the volatile content was 55% for the primary and 45%
for the secondary.
Effect of Sludge Accumulation on Aerated Lagoon Performance

During the months of May, June, July and August 1969, in all three systems, there were significant
upward  trends in the effluent BOD, as shown in Figure  11. All three systems showed similar
relationships. This decline in  BOD removal efficiency was accompanied by a trend to reduced
dissolved oxygen concentrations in all cells. The reduced dissolved oxygen could be an "effect"
caused by high oxygen demands imposed by the end-products of anaerobic decomposition of the
sludge, or it could be a "cause" of higher effluent BOD due to an oxygen deficiency.

-------
200
Some  of  the  related factors that may account for the sludge accumulation  and the effect on
performance are:

     a)   Release of sludge digestion end products to the mixed liquor
     b>   Recycle of sludge by bacterial and algal synthesis in the mixed liquor
     c)   Relatively short period of higher rate anaerobic digestion
     d)   Insufficient air supply

The duration of the study has been insufficient to allow definition of the ultimate extent of sludge
accumulation and loss of efficiency during the summer. However, based on the observations made,
it appears that sludge is accumulating at the  rate of approximately one ton of dry solids per Imgd
treated.
To  determine if  an abnormal  quantity of inert material was contained in the raw sewage  or
effluent a series of tests was conducted. The volatile content of the raw sewage was normal and
showed no evidence of extraneous inert matter. Similarly, the effluent volatile solids were typical
for  biologically treated sewage.

Insofar  as  the higher BOD and reduced D.O. in the effluent is concerned, it is probably that
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                         FIGURE 6  Temperature monthly average

-------
                                                                                     201
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sufficient additional air can be added economically to handle the benthal demand, although some
doubts exist because the Surface Aerator system sustained a similar loss of efficiency in spite of
relatively higher D.O.  concentrations. The  major problem would appear to be  the  physical
accumulation of the sludge, which will ultimately require removal and additional treatment.

Sawyer has described the problems encountered as being similar to experience with Imhoff tanks,
with respect to removal and storage of BOD and  solids during the winter months and the release of
soluble  BOD and  nutrients  as  acid fermentation of  accumulation  sludge deposits develops.
(Sawyer, 1970).

                   OPERATIONAL OBSERVATIONS AND  PROBLEMS

Observations were made on mosquitoes, weeds,  grease and scum odors, ice, foaming, grit, erosion
and  equipment operation. Plugging  of the  Air-Aqua tubing and  the Air-Guns  occurred. The
problems were  corrected  and  at  the  time of writing,  both  systems  appear to  be operating
satisfactorily, although  more  time  is needed to assess their  ultimate  reliability. Ice was a major
problem  with operation of the surface aerators; ice  built  up on the impeller shaft and support
structure with subsequent freeze-up and stoppage. Although steps were taken to try and eliminate
the ice problem, it was found that during the winter months only half of the surface aerators could
be kept operating.

-------
  202
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                                                                                       203
cell which at times released odors that were quite noticeable on the enclosing banks. They were
attributed to the floating grease and scum collecting along the banks and in the corners of this cell,
where this material would decompose,  releasing  odors. This occurred primarily along the south
banks, and may well have been the result of the very flat slope (8:1 > incorporated in the design.

Ice

Ice build-up caused the greatest  problems with the  surface aeration system.  The Air-Aqua and
Air-Gun systems were notably free of problems due to ice build-up.

The Air-Aqua system did not cover completely  with ice for the winter period and  showed the
peculiar build-up of "stooks" over the air lines  as observed in other installations. Ice thickness
found on  the Air-Aqua secondary cell varied  from approximately 6 inches to 48 inches from inlet
to  outlet, respectively.  With water depth of  10 feet this will  cut down  the retention period
considerably  during  the  winter  when  water  temperatures are adverse to  the  promotion  of
biological  activity.  The  foregoing is  of course true  for all  lagoon  type systems,  be  they
conventional or aerated.  No ice  thickness surveys were carried out  on the remainder of the test
cells due to thin ice.

The Air-Gun  system retained  open water longer than the Air-Aqua. With the  onset of colder
temperatures  the  openings immediately above  the guns  decreased  in size from inlet to outlet.
Under severe  temperature conditions the  openings became covered with ice domes  towards the
outlet end. Open water conditions existed year-round above the first two or three rows of guns.
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                  FIGURE 9  Test aerated lagoons average test results nitrogen

-------
204
Ice built up on the surface aerators to such an extent that  it was impossible to clear the ice from
the aerator area. The result was that during the winter only three or four surface aerators could be
kept operating.

Foaming

As with conventional  lagoons or stabilization ponds, foaming conditions were  encountered to
some degree with all three aeration systems. The surface aeration system showed  more foam than
the  other  two systems, due  to the more violent agitation of the  surface of the water by the
aerators.

The  quantity of foam  generated  varied  with  the water temperature, the  maximum  condition
occurring after spring break-up when  water temperatures were rising.  However,  the foaming did
not reach a point where  it became a problem
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 Grit and Rags

 After  one year of operation considerable  quantities of grit and rags were  present in all three
 systems. For the effective long-term operation of any aerated system pre-treatment facilities will
 be required to remove grit and rags.

 Bank Slopes

 The following observations on bank slopes were made:

-------
                                                                                       205
The existing 8:1  slope  utilized  in the Air-Aqua cells created a wide unaerated  band around a
portion of the lagoon; this likely resulted in some short circuiting.  If flat slopes are required for
stability, consideration should be given to providing aeration along the slope. The majority of the
dikes for the demonstration lagoons were constructed at 3:1;  this  slope was  stable,  but for
long-term operation 4:1  is recommended. The slopes of the Air-Gun  cell were constructed at 2.5:1
to minimize surface area. These slopes proved unstable  under draw-down conditions. The rip-rap
provided effective erosion control in all cells.

Equipment Operations

Air-Aqua System.  After start-up, difficulties were  encountered  with pressure build-up in  the
system. Recommended HCi acid gas cleaning of the tube system was performed without alleviating
the  problem. Removal of a 250-foot length of tubing revealed that the perforations had not been
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-------
 206


 properly cut. All tubing was repunched in situ, requiring the lowering of the system so that the
 workers could walk through the cells feeding the tubing through a punching mechanism mounted
 on a boat. The repunching took 2 man-days to complete.

 Upon completion of this work, pressure on the system dropped to 5.6 to 6 psig. The manufacturer
 then recommended that acid cleaning be carried out quarterly, regardless of pressure build-up.

 When operating properly, the pattern of air distribution should show a grid of air bubbles, released
 by  the perforated  tubing. Although this grid did show immediately after  installation and
 repunching  of the  tubing, it  deteriorated after a period of operation due to clogging of the
 perforations, regardless of  acid cleaning, carried out regularly. This clogging had affected the air
 distribution pattern  and was confirmed by D.O. tests. Further investigations traced  the loss of
 pattern to water in the tubes and condensation, and from water coming back through the valves
 during power failures.  By manipulating the acid valves it was possible to force the majority of the
 water out of the tubes, restoring a reasonably good air pattern.

 Supporting  equipment such as  air-compressors,  effluent recirculation  pump, flow meters, and
 samplers were subjected to a regular  preventative maintenance program, and few problems were
encountered.

Surface Aeration System. Ice has been a problem with the operation of the surface aerators. The
 basic  problem was ice build-up on the impeller shaft and supporting structure, with subsequent
 freeze-up and stopping of  the mechanism. Ice  formed  on the  piles and impeller, resulting in a
 limited clearance between the rotating ice on the impeller and the fixed ice on the piles. This is a
 problem that is difficult to overcome with the winter climate experienced in the Winnipeg area.
Two methods aimed at overcoming this problem were attempted; firstly, one of the platforms was
 shrouded with plywood, and secondly a second unit was shrouded with flexible nylon cloth. Both
attempts failed.

 Other  results of the  ice accumulation were off-balance, causing vibration of the supporting
structure and misalignment of motor reducer,  resulting in a coupling failure and loosening  of
 impeller, bending and loss of blades.

 In the spring of 1968 the manufacturer replaced all blades with a heavier design. Although this was
thought to cure the  problem encountered with the impeller blades, subsequent winter operation
disproved this, as bending and loss of blades occurred.

 It may be  possible  to  reduce or eliminate the  icing problems  with a  change  in the supporting
structure. The existing structure with  four piles provided a surface for the ice to grow on, a two
 pile arrangement with the piles widely spaced may be more successful.

Air-Gun System. No problems were encountered with the operation of this system until October
 1968.  when  it was  noticed that the most northeasterly gun was discharging air continuously.
 During the winter  1968-69 this condition spread to most guns. It was thought to be caused by the
 build-up of either ice or rags in the syphon chamber. The latter proved to be true. In May 1969,
 the manufacturer installed syphon chambers of  a new design on 42 guns. The new design, having
 larger  clearances, may  eliminate the  problems  of plugging of the syphon  chambers with rags.
 Insufficient time has elapsed since the modification to allow an  assessment of their long-term
 dependability.

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                                                                                       207


                                          COSTS
Capital Costs
Two sets of cost data have been prepared for aerated lagoons; firstly, the 0.5 Imgd demonstration
lagoons and secondly, a general unit capacity cost curve.

All  costs  and estimates in this report are  adjusted  to an Engineering News  Record Sewage
Treatment Plant cost index of 132.0. As costs change the appropriate adjustment must be made to
the reported costs.

The  capital costs for the demonstration  lagoons are shown in Table 2. These costs have been
arrived at by  assuming each system would be as indicated in Figure 1, insofar as floor dimensions
and  identical  equipment layout are concerned. However, in order to relate realistic costs to a
permanent  installation it is necessary  to  assume each  unit is to be  constructed  as  a  totally
independent unit. An independent unit is one  with  independent piping, diking, influent-effluent
structures and electrical  supply. Therefore, only items  1  and 2  of Table 2 are established directly
from  the  contract  amounts.  The  remaining  items were  arrived  at by combining  estimated
quantities and the actual unit prices tendered. The general contractor for the lagoon project was
consulted on  the tendered prices. All  costs were considered realistic with the exception of rip-rap.
In the case of rip-rap, the contractor was of the opinion that  the price should be 1.5 times  the
tendered price (i.e. $12.00/cu. yd. in place).

The estimated quantities for earthwork  were calculated on the  basis of 3 feet freeboard, 12 feet
roadway width, and 4:1 dike slopes, rip-rap facing the interior  dikes from toe of slope  to 1 foot
above  the  normal  operating  level. These  adjustments are considered  necessary  to  insure  a
permanent  and  relatively maintenance-free structure with the soils encountered in the Winnipeg
area.

Sodding and seeding quantities include sodding  the interior dikes above the rip-rap and 50% of the
total dike crest, and seeding the exterior dike slopes. Roadway quantities are based on an asphaltic
surface treatment being applied to the unsodded dike crest.

The  electrical costs include  service entrance  equipment, motor starters, and lighting for  the
equipment  and  structures associated with  the  respective systems. Power distribution costs were
based on the  billing received from Manitoba Hydro for the supply and erection of equipment, and
allocation to the respective systems on the basis of length of cable  and number of poles required
for each.

Actual influent  and effluent chamber and piping costs were reestimated on the basis of piping and
chambers being of such length and size for an independent treatment system of 0.5 Imgd capacity.
Fencing costs are for the perimeter of the cell taken at the toe of the dike slope. Additional items
of chlorination  facilities and instrumentation  are included since these  would be desirable in a
permanent  installation.  The costs do not  include pumping station, forcemain, outfall, or land.
However, they are inclusive of engineering, legal and administration charges.

From Table 2  it can be seen  that the total costs for the Air-Gun are slightly  lower  than  the
Air-Aqua and Surface Aerator  Systems. Major cost differences are  due to additional rip-rap and

-------
 208

                                        TABLE  2
                           Capital Costs - Demonstration Lagoons
                                                                Surface
                                               Air-Aqua         Aerator         Air-Gun
 1. Aeration Equipment, Supply
      (Blowers, Headers)                        $ 47,500         $ 44,300         $ 38.0001
 2. Aeration Equipment, Installation
      (Headers, Housing, Platforms)                 23,000           56,500           33,700^
 3. Electrical                                     3,500            7,800            3,500
 4. Influent Piping                                3,200            3,200            3,200
 5. Effluent Piping                                3,500            2,200            2,200
 6. Influent Chamber                             17,900           17,900           17,900
 7. Effluent Chamber                             22,900           22,900           22,900
 8. Excavation & Dike Construction               32,400           29,200           27,000
 9. Clearing, Grubbing Unsuitable Material          10,800           10,800           10,800
10. Rip-rap                                      93,000           73,500           70,300
11. Seeding & Sodding                             6,400            5,000            4,000
12. Roadway (asphalt)                             3,900            3,500            3,200
13. Chlorination Facilities (including
      housing)                                    20,000           20,000           20,000
14. Power (hydro)                                 3,500            5,400            3,500
15. Instrumentation (including magnetic
      flow meter)                                 10,000           10,000           10,000
16. Fencing                                       4,700            4,000            3,500
Total  Estimated Cost                            $306,200         $316,200         $273,700
10% Eng. & Contingencies                          30,600           31,600           27,300
Total  Estimated Cost                            $336,800         $347,800         $301,000
Costs  indexed to ENR S.T.P.       1) Includes installation, excludes blowers and header
il
cost index 132.0                 2) Includes blower and header
excavation required for the dividing dike, greater dike perimeter for the Air-Aqua System, and
platform costs for the surface aerator.
Figure 12 shows the development cost of the aerated lagoon process per  unit of lagoon capacity.
These  costs have been  developed by applying the unit material and installation costs of the
demonstration  lagoons  to  calculated quantities. Equipment supply and installation costs  were
derived from equipment manufacturers' quotations for similar facilities at other treatment works.

-------
                                                                                       209
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                  FIGURE 12 Aerated lagoons capital cost vs. design capacity

Operation and Maintenance Costs

The operating and maintenance costs for the 0.5 Imgd demonstration  lagoons are shown on Table
3. They are based on 17 months of operation.

Assuming chlorination of the effluent at 8 mg/l is desirable, the total operating costs should  be
adjusted to $53, $107 and $56 for the respective lagoons.

The power costs tabulated in Table 3 are based on field measurements of true power drawn with a
unit  power cost of 0.9c/kwh. Allocated to each system is a shore of the heating  and sampling
pump load. In the  case of surface  aeration the cost is calculated on all eight units  operating.  In
terms of oxygen requirements, the  surface  aerators are capable  of treating in excess of the rated
flow.  However, at the time of design, eight units were considered necessary to insure adequate
mixing.

Repairs include regular weekly  inspection  and  servicing of equipment, non-routine  repairs and
replacement parts  where required.  The costs of repunching the  aeration tubes  and  replacing the
siphons on the Air-Guns are not included in Table 3. The labor and materials on  the servicing were
based on  actual time card and material  receipts and allocated to  the respective systems.  Labor
includes a 25% factor  for  overhead.  General  costs include maintenance to the common inlet
chamber,  metering equipment, etc. Since  it  was difficult to allocate these costs to a specific lagoon
they were split equally  to the three  systems.  Laboratory costs include  labor and supplies for

-------
210


                                       TABLE 3

                          Actual Operating and Maintenance Costs
                             0.5 Imgd Demonstration Lagoons

                                                      Avg. Cost per Img Treated
                                                               Surface
                                            Air-Aqua           Aerator           Air-Gun

Power                                           $ 10             $  64              $ 15

Equipment Servicing & Repair                       13                14*               12

Laboratory & Control                              13                13                13

Road & Dike Maintenance                            433

Snow Removal, Grass Cutting,
 Mosquito Control                                   333

General                                             333

Total Operating & Maintenance Costs
 per Imgd Treated                               $ 46             $100              $ 49

*Not continuously maintained due to ice.
 sampling and analysis. Actual  laboratory costs were three times the cost reported due to the
 frequency and number of analyses performed under test conditions. Therefore, the lower costing
 for laboratory reported here would be a more realistic value under normal operating conditions.
 Maintenance and laboratory personnel were not based  at the lagoons during the test; therefore
 considerable labor and vehicle time for travelling were not charged to the test lagoons.

 The development of operating and maintenance costs for aerated lagoons is shown in Figure 13.
 The curve was prepared by projecting the actual demonstration lagoon costs on the trend line as
 indicated. The slope of the line  was guided by costs reported in recent  literature  (Okey and
 Rickles, 1968). The reported costs from the literature  reference have been adjusted to  Imperial
 Gallons and are also shown  on  Figure  13. It  is noteworthy that the  referenced costs are
 representative of power costs of 1  c per kw. hr. and labor of $5.00/hr., while in comparison the
 local power and labor costs are approximately 0.9 c per kw. hr., and $4.25 per hr., respectively.
 Very little cost information at other aerated lagoons is available to confirm the trend costs for
 increasing capacities. However, a check was made on the expected operating and maintenance
 costs by determining the future  power requirement for  mechanical equipment coupled  with
 current power rates. The total costs were extrapolated from the power costs on the basis of power
 being about one-third of the total  costs. This provided a reasonable check on the trend developed
 by the literature.

                                     CONCLUSIONS

 Aerated lagoons were found to be capable of providing "secondary equivalent" sewage treatment.
 Under prairie climatic conditions there is a problem of sludge accumulation leading to a decline in
 efficiency of BOD removal and a reduction in  the dissolved oxygen concentration during the
 summer months.

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                                                                                        211
The economic feasibility of aerated lagoons is questionable until the extent and cost implications
of the sludge problem are fully defined by further research and experience.

The use of surface aerators under prairie winter conditions is not practical due to ice build-up

ft can be concluded  that aerated  lagoons are an effective means of providing secondary treatment
but some provision must be made for sludge handling.

It is intended to continue the investigation on a less rigorous scale, with a goal of determining the
long term effects, and finding a practical and  economical solution. Equipment manufacturers are
actively pursuing a solution.
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               FIGURE 13 Aerated lagoons operating and maintenance costs

-------
212
                                     REFERENCES

Azzenso, J. R. and Reid, G. W., Removing  nitrogen and phosphorus by bio-oxidation ponds in
    centra! Oklahoma, Water and Sewage Works, V. 113, No. 8, p. 294-299.

Barn hart, E. L. and Eckenfelder, W. W., Jr. (1965) Theoretical aspects of aerated lagoon design,
    paper presented at the Symposium on Waste-water Treatment for Small Municipalities, Ecole
    Polytechnique, Montreal, pp. 1.

Clark and Oostal (1968) Evaluation of waste treatment Chemawa Indian School, Report No. FR-6,
    FWPCA, North West Region, Pacific North West Water Laboratory. Corvallis, Oregon.

Okey, R. W. and Rickles, R.  N.  (1968) Industrial waste treatment management. Water and Waste
    Engineering, Vol.  5, Nr.  9, pp. WWE/1-14.

Sawyer, C. N. (1970) Private communication.

Thimsen, D. J. (1965) Biological treatment  in aerated lagoons. Paper presented at the Twelfth
    Annual Waste Engineering Conference, University of Minnesota.

-------
  DESIGN  CONSIDERATIONS  FOR  EXTENDED  AERATION IN ALASKA


                  Sidney E. Clark, Harold J. Coutts and Conrad Christiansen


                                     INTRODUCTION

Alaska is the largest state of the  United States, sparsely populated and with a variety of climates,
including  arctic,  sub-arctic,  marine  sub-arctic  and temperate. The  population is small  and
widespread with 294,417 people  (preliminary 1970 census figure) inhabiting 586,000 square miles
of land area.  Settled areas requiring  domestic  sewage  treatment include large municipalities,
military installations, remote  sites and villages, each of  these having different requirements and
presenting different problems.

Construction and power costs in Alaska are very high in general, and excessively so in remote areas
(1.5 to  5  times Seattle  construction costs  index). Skilled personnel for operation of treatment
plants are scarce and, in most cases, nonexistent.

The effect of man's waste on arctic and sub-arctic ecosystems has received little attention in the
past and is not well understood. Because of recent increased interest in the Arctic region, some
information is now  becoming available  on man's possible  influence.  For example, during the
winter, dissolved oxygen (DO) of ice-covered Alaska rivers may reach extremely low levels of 3
mg/l   or  less  under  natural   conditions  (Frey,  1969;  Gordon,  1970; Roguski,  personal
communication). Because of the  retarded ability  of Alaska streams to replenish DO under total or
nearly  total ice cover, it becomes essential  that the natural balance not be upset by  man. Under
these  conditions,  secondary sewage  treatment  will be  required  to assure  adequate stream
protection.

One of the major advantages of biological processes for provision of secondary  treatment is their
ability to  oxidize waste  without large inputs  of energy, thus  reducing shipping costs, etc.,
associated  with  materials  required  for  chemical treatment.  All factors  considered, extended
aeration systems have considerable potential for reliable and economical secondary treatment at
larger governmental installations  and large communities in  Alaska (populations greater than 250).

Current extended aeration research is being conducted by several groups:

     1.   Corps of Engineers
         Cold Regions Research and Engineering Laboratory
         Alaska District

     2.   University of Alaska
          Institute of Water Resources

     3.    Federal Water Quality Administration, Alaska Water Laboratory
         Cold Climate Research  Program
                                            213

-------
214


Waste treatment research at the Alaska Water Laboratory is concerned primarily with adapting
methods developed in the contiguous United States to the extreme cold climates found in Alaska.
The scope of the present work on activated sludge is, in general, limited to extended aeration, and
includes investigations in the following areas:

     1.   Low temperature biokinetics

     2.   Low temperature solids removal

     3.   Degree of environmental protection required for equipment and processes.

     4.   Aeration requirements

     5.   Aeration chamber mixing

     6.   Waste sludge characteristics and disposal

The above investigations are being conducted on a laboratory and pilot plant scale. Monitoring of
existing facilities is also taking place.

                       LITERATURE AND  EXPERIENCE  REVIEW

 Low Temperature Biological Treatment Feasibility

Although the activated sludge process is  affected  by temperature,  operation at temperatures
approaching freezing is feasible. A number of investigators have reported a considerable amount of
biological activity taking place at freezing temperatures  and  below  (Ayres, 1962; Halvorson,
 1962).  Miller (1967) has reviewed the information available on microorganisms indigenous to cold
environments and found that research on psychrophilic  organisms is still in the initial stage, but
 concluded that "truly  psychrophilic microorganisms do exist and are distinguished by their ability
 to grow at very low temperatures and to do so at rates comparable to those of mesophiles at higher
 temperatures." The  feasibility  of effective biological treatment by full-scale  extended  aeration
facilities at operating  temperatures as  low as  2°  C has  been demonstrated (Anonymous, 1965;
 Grube and Murphy, 1968; Schmidtke, 1967).

 Temperature Effects

Pasveer (1955) conducted laboratory scale temperature studies with activated sludge and reported
that the process goes on almost as well  at 3° - 5° C as it does at 20° C. Wuhrmann (1956) found  in
his studies  of  the activated sludge  process that "the BOO removal  seems to be  only  slightly
influenced by temperature, whereas nitrification  is markedly higher in summer than in winter."
Ludzack (1965) conducted bench scale studies using a continuous apparatus with a detention time
of 24 hours and a loading of 35 Ib. COD/1,000 ft3 and demonstrated COD removal efficiencies of
<90% at 21° - 25°  C. 90%  at 10° C  and 84% at 5° C. Hunter et at. (1966) conducted batch
operated laboratory scale studies on the effect of temperature and retention times on the activated
sludge  process. At temperatures between 4°  C and 45° C, they found little  change of BOD or
suspended  solids removal efficiencies. As the temperatures increased, they found less filamentous
growth  and  increased  protozoa and rotifer populations. Grube and Murphy (1968) evaluated an

-------
                                                                                      215


oxidation ditch and found BOD removal efficiencies greater than 90% with liquid temperatures of
2° C, air temperatures ranging down to -40° C, and average detention times of 2.3 days. Influent
temperatures averaged  16.6° C with a  minimum of  7.5° C. Gustaffson and Westbury (1965)
evaluated the activated sludge process for application at Kiruna, Sweden, and obtained 75% BOD
reduction with a 31/2 hour detention time system at 2.8° - 4.8° C and 2,700-3,500 mg/l MLSS.

Temperature Coefficient

The temperature coefficient, 0, is used in the relationship

                                    ki/k2  = B (t, -ta)

to define the effect of temperature  on biological  activity. The values Iq and k2  refer to velocity
constants at  temperatures t,  and  t2  respectively. The  value  of 6  indicates the extent of  the
temperature effect  on the biological activity. Use of this equation, known as  the Arrhenius
relationship, to define the effect of  temperature on wastewater and reaction rates, dates back to
Streeter and  Phelps (1925) and Theriault  (1927), who reported 6 values of 1.047 for domestic
wastewater  and river water  (Zanoi, 1969). Pohl  (1967) concluded that 6 was dependent on  the
mixed  liquor concentrations: 9 = 1.038 at low MLSS and  1.000  at high MLSS.  Benedict (1968)
conducted studies in the  temperature  range of 4° - 32° C and concluded 6 (0 = 1.078 @ 4° C) was
independent of loading when the loading rate did not exceed 0.53 Ibs BOD/day/lb/MLSS, but 6
increased as loadings above  0.53 were imposed.  Eckenfelder (1967) suggested that0, based on
overall  treatment  efficiencies, was a function of the  organic loading and reported 0 values  for
activated sludge of 1.00 at low loadings and 1.02 at high loadings.

Solids Separation

Solids removal  plays a very important part in the  efficiency  of the activated  sludge treatment
process. The  degree  of sludge  separation  directly  influences  the quality of  effluent  from
wastewater  treatment plants with higher concentrations of effluent solids  contributing to high
effluent BOD. Reed and  Murphy  (1969)  conducted an investigation  on  settling characteristics of
activated sludge at temperatures  ranging from  1.1° to 23.4° C and found that the influence of
temperature on settling  velocity decreased as the  concentration increased. They developed an
equation for zone settling based on  experimental  data. They also suggested upflow sludge blanket
clarifiers as having greater potential for cold  regions application. Benedict (1968)  suggested that
the effect of sludge settleability on  gross COD removal was magnified at low temperatures and as
the loading rate was increased.

Hansen  (1967)  reported  on  a  method of solids separation which successfully employed shallow
depth sedimentation theory. The  settling units consisted of small diameter tubes  (1-inch) inclined
at 5° and 2-4 feet in length. Detention times were very short and backwashing was necessary  for
removal of accumulated solids. Hansen (1967) also reported on the use  of steeply inclined tubes
(60°)  which  permit solids deposited in the tubes to  continuously slide  down  by gravity. A
secondary clarifier of a trickling filter plant was converted  to a biological reactor and the steeply
inclined tubes utilized for solids  separation which increased plant efficiency from 85% to more
than 95%. The effluent suspended solids averaged 70 mg/l varying from a low of 7 mg/l to a high
of 190 mg/l, which was comparable to that produced by a conventional clarifier of an extended
aeration plant of the same capacity  (3000 gallons per day at 12-hour detention). Other reports  are

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216
available which describe the use of tube settlers in water treatment and waste treatment solids
separation (Gulp, 1969; Senlecta and Hsiung, 1969).

Pohl (1970) investigated tube settlers in the laboratory and obtained  the best results at room
temperature but found the tubes passing excessive collodial solids occasionally.

Design Parameters

Little information  is available on biological treatment process design for temperatures less than 5°
C. Ludzack (1965) and Hunter, et al. (1966) observed that excess MLSS accumulation increased
with decreasing temperature. The cell yield (c) increases with increasing temperature because it is
believed a larger portion of BOD removed is utilized for energy at low temperatures than at high
temperatures  (Stewart,  1964). -Since  the  rate  of endogenous respiration  is depressed  at  low
temperatures,  the quantity of excess sludge produced is increased. Benedict (1968) reports values
for c and k (endogenous rate) at 4° C of 0.42 mg/mg CODr and 1.32% respectively.

Aeration

Eckenfelder and O'Connor (1961) stated  that the temperature coefficient 6, when applied to
oxygen transfer efficiencies, has been reported  to vary from 1.016 to 1.047  and that studies on
bubble aeration indicated a temperature coefficient of 1,02 applied. The  effects of temperature on
stream reaeration have been studied under controlled experiments in the laboratory (Anonymous,
1961). A value for 6 of 1.0241 for the temperature range of 5° to 30° C was found. Black (1968)
described a procedure for evaluation of  aeration devices and stated  that a 6 value of 1.030 or
higher should be used for cold water.

                                 LABORATORY STUDIES

During the past two years, three bench scale activated sludge reactors have been utilized for
kinetics and solids separation  studies. The three units are illustrated  in Figures  1, 2, and 3. The
systems have  been operated as continuous flow systems with the feed being primary effluent
                            Mnr
                                                         Conwrtrtc Ctnn
                 FIGURE 1   Cone reactors (as manufactured by Pope Scientific)

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                                                                                       217
                                                                    Reactor
                                                                   Sid* Vi*«
                              FIGURE 2   AWL reactor (8.9 gal.)


brought to the laboratory from  the Eielson primary sewage  treatment  plant. Routine analysis
included influent and effluent BOD and COD, mixed liquor and effluent suspended solids (SS) and
volatile suspended solids (VSS). Nutrient analyses of the influent and effluent samples were made
weekly  and  included  ammonia,  nitrite,  nitrate,  organic  nitrogens,  total  phosphates, and
orthophosphates. A limited number of coliform counts were  made on the influent and effluent.
Microscopic examinations of the reactor contents were made  on an  irregular basis at times when
apparent or suspected changes in the mixed liquor had taken place. The examinations consisted of
general observations on the relative quantities of protozoa present and the degree of activity. BOD,
COD, and solids analyses were done in  accordance with Standard  Methods procedures (1965).
Coliform counts were made by the membrane filter method as described in Standard Methods and
nutrient analyses were made in accordance with Federal Water Quality Administrations Standards
(1969).

The cone reactors (Fig. 1), when operated at 1.3° C and 6.5°  C for long periods of time, showed
some interesting characteristics which  are summarized in Tables 1 and 2. Both biological sludges
were relatively easy to establish.
                         Air Suppy
                                                                      l-teTimer
                                                                jj[s ienoki*vav«*

                                                                      24-hr
                                                                      Timer
                                                                Recycle
                                                                Pump (Hotter)
                                                                    Effluent Tank
                                                                     2 Tube
                                    Moisture
                                     Trap
                              FIGURE 3  AWL reactor (12.45 gal.)

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218


The  reactor  runs  started with  the longest  detention  time  first  and the times decreased in
chronological order. The  1.3° C reactor took a considerable amount of time to establish a stable
system  (more than 3 months).  However, a good removal  rate was obtained before the  MLSS
stabilized. There was apparently little difference in the biological activity at the two temperatures,
but operation of the reactor at 6.5° C was more erratic.

Both reactors generally showed "auto-induced sludge wasting" in the same manner as the College
Utilities oxidation  ditch described by Grube and Murphy (1968). The MLSS would build up to a
point and begin  to pass solids for 1 or  2  days and then repeat the cycle. The cycle was repeated
within 2 to 3 weeks as opposed to the monthly occurrence reported by Grube and Murphy.

The reactors differed in their manner of passing solids, with the 1.3° C reactor genera My having a
much more turbid effluent and the 6.5° C reactor having a relatively clear effluent. Heavy solids
passed from the 6.5° C reactor by rising in the settling tube as a solid mass. As the concentrations
of solids in the mixed liquor increased,  the level of solids in the settling tube would rise until
spilling over into the effluent tank. After passing an undetermined amount of solids, the cycle
would be repeated. A gradual drop in pH  was noted in the 6.5° C unit as the suspended solids
began to build before discharging. The  pH dropped from slightly above 7 to values of 6.6 to 6.7.
pH of the  1.3° C unit consistently remained around 7.4. The 6.5° C effl ent solids settled to the
bottom of the effluent tank leaving a clear liquid above, whereas, the 1.3° C effluent solids did not
settle to any degree. As the 1.3° C reactor became more stabilized, the effluent became less turbid
                                        TABLE 1

                                      Data Summary
                                    1.3°CCone Reactor
                                Feed:  Primary Plant Effluent

 Detention
  Time(hrs)                         21              15               13                9

 Influent
  BOD(mg/l)                       111             170              201              184

 Reactor
  Susp. Solids (mg/1)               1,074           1,561            2,657            2,926
  Volatile
  Susp. Solids (mg/1)                 890           1,324            2,212            2,402

 Filtered Effluent
  BOD (mg/1)                        37              11               20               14
  % BOD Removal                    66              93               90               92

 Unfiltered Effluent
  SUSP.  Solids (mg/1)                  29              43               38               82
  BOD (mg/1)                        40              62               28               44
  % BOD Removal                    64              64               86               76

 Loading Factor
  Ib BOD Fed
  IbMLVSS-Day                     .19              .21              .17              .20

Product of
  MLVSS and Det. Time           14,700          19,500           28,000          21,600

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                                                                                     219


and the MLSS began to increase. The 6.5° C reactor operation was less stable, with the maximum
level of MLSS generally not rising above 2,300 as opposed to 3,000 for the 1.3° C MLSS. Results
of nutrient analyses are presented in Table 3. There was a significant change  in nitrate and total
nitrogen at 6.5° C when going from 9 to 13 hours detention time. This was also true at 1.3°  C to a
lesser degree. There was a greater reduction in ammonia nitrogen and a greater increase in nitrate
nitrogen at 6.5° C. Ammonia was essentially not affected at 1.3° C. Total nitrogen removals were
much higher at 6.5° C than at 1.3° C with little detention time effects.

Overall results of operation of the 8.9 gal. and 12.45 gal. reactors are presented in Tables 4  and 5.
Temperature  changes were  accomplished by a  gradual  increase  or decrease  in the  constant
temperature room temperature. These reactors were operated at 12-hour hydraulic detention times
with daily sludge wasting to maintain  the MLSS at 4,000 mg/l. The 8.9 gal.  reactor was later
converted to a 24-hour operation.  Sludge was wasted by drawing  off the required amount of
mixed  liquor. A portion was used for a solids analysis to determine the exact amount of solids
removed. The effluent BOD and COD figures of 9 to  21  mg/l  and 46 to 96 mg/l indicate  that a
considerable amount of biological activity takes place at low operating temperatures.

Effluent BOD/COD ratios varied from 0.13 to 0.27,  indicating that effluent organics were well
oxidized. These were in comparison with the influent BOD/COD ratios of 0.55 to 0.66.
                                        TABLE 2
                                      Data Summary
                                      .0
                                   6.5  C Cone Reactor
                                Feed:  Primary Plant Effluent

 Detention
  Time(hrs)                          17               15               13               9

 Influent
  BOD (mg/l)                       139              132             153             155

 Reactor
  Susp. Solids (mg/l)               2,346            1,885            1,880           2,285
  Volatile
  Susp. Solids (mg/l)               1,915            1,563            1,587           1,801

 Filtered Effluent
  BOD (mg/l)                      51.3             16.3             13.3            11.7
  % BOD Removal                    63               88               91              92

 UnfUtered Effluent
  Susp. Solids (mg/l)                  11               69               96              45
  BOD (mg/l)                        53               36               31              33
  % BOD Removal                    62               73               80              79

 Loading Factor
    Ib. BOD Fed
  Ib.MLVSS-Day                     .08            .106              .18              .23

 product of
  MLVSS and Det. Time          31,600          23,000           23,300          20,600

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220
                                        TABLE  3
                         Cone Reactors Results of Nutrient Analysis

                                 13 Hour Detention Time

                                 1.3°C REACTOR
                                     6.5°C REACTOR
                          Influent   Filtered   Unfiltered   Influent   Filtered   Unffltered
                                     Effluent    Effluent              Effluent    Effluent
NH3-N (Ammonia)
NO2-N (Nitrite)
NO3-N (Nitrate)
KJeldahl-N (Nitrogen)
Total (Nitrogen)
Total Nitrogen
  Removals (%)
O-PO4 (Ortho-Phosphate)
   22
  .13
  .13
   41
41.26
   20
   19
  .09
 2.13
   28
30.22

   27
   18
   18
  .05
 2.02
   29
31.07

   25
   18
   19
  .11
  .21
   37
37.32
   19
      1
     .13
   9.17
      3
  12.30

     67
     18
        1
      .15
    12.13
        3
    15.28

       59
       18
9
1.
Influent

Hour Detention Time
3°C REACTOR 6
Filtered
Effluent
Unfiltered
Effluent
Influent

 NH3-N (Ammonia)
 NO2-N (Nitrite)
 NO3-n (Nitrate)
 Kjeldahl-N (Nitrogen)
 Total (Nitrogen)
 Total Nitrogen
  Removals (%)
 O-PO4 (Ortho-Phosphate)
   21
   .06
   .11
   36
36.17
   17
   19
  ,,03
  .68
   26
26.71

   26
   14
   19
   .03
   .54
   27
27.57

   24
   15
                                                                  6.5 C REACTOR
   21
  .06
  .07
   35
35.13
   19
Filtered
Effluent

       1
     .14
    8.03
       3
   11.17

     68
     18
Unfiltered
 Effluent

        1
      .12
    14.45
        3
    17.57

       50
       16
 (1) Total nitrogen results reported are the sum of the nitrite and Kjeldahl nitrogen analysis.
 The amounts of sludge wasted varied from 0.42 mg susp.  solids/mg BOD removed  at the low
 temperatures to 0.14° to 10.5° C and 24-hour detention time. The pH of both reactors ranged
 from 7.2 to 7.6 during the sample periods reported.

 Poor settling sludges were developed during operation of these reactors with the Sludge Volume
 Index  (SVI) consistently ranging above 200. The sludge produced appeared to be of a zoogloeal
 type similar to that reported by Heukelekian and Wiesburg (1965) who found a direct correlation
 between increasing SVI and increasing bound water for this type of bulking. Very little evidence of
 Sphaerotilus was noted during microscopic examination. Ludzack  (1965) also reported  a poor
 settling sludge at low temperatures (5° C) with very poor drainability.

 The significance of protozoa in an efficiently operating activated sludge process, as reported  by
 McKinney  (1956), was observed during operation of the reactors even at the coldest temperatures.
 The 12.45 gal. reactor was  seeded  at temperatures <2° C with return sludge from an oxidation
 ditch treating domestic sewage. Initially, the effluent was very turbid as the sludge was acclimating

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                                                                                    221
                                         TABLE  4

                        Summary of Results of 8.9 Gallon Reactor and
                           12.45 Gallon Reactor at 12-hr Detention

                                Feed: Primary Plant Effluent
 Reactor MLSS (mg/1)
  %VSS
  BOD
  COD
 Loading:
            Ib. Infl. BOD
          lb MLVSS-Day

 Sludge Wasted:    mg/MLSS
               rag BOD Removed
 Unfiltered Effluent
  Suspended Solids (mg/1)
  BOD (mg/1)
  BOD Removal (%)
  COD (mg/1)
  COD Removal (%)

 BOD/COD Ratio
  Influent
  Effluent
  Reactor
                                            REACTOR TEMPERATURE (AVG°C)
4160
  80
2489
5648

 0.12
                                       0.42
  18
  21
  89
  78
  76
0.60
0.24
0.44
 2.9

4097
  80
2503
5788

 0.10
               0.33
   3
  13
  92
  46
  73
0.60
0.23
0.43
 3.8

4076
  81
1477
5260

 0.10
               0.32
  12
  17
  90
  67
  78
 0.55
 0.25
 0.28
 8.0

3737
  80
1299
4705

 0.14
                                                                                 0.33
   5
   9
  96
  96
  83
 0.66
 0.16
 0.28
itself to the new conditions. The  decreasing turbidity of the sludge as acclimation progressed
corresponded to  increasing  numbers  of protozoa, generally  Paramecium  and Vorticella. As
reported by McKinney (1956), a very well-stabilized activated sludge system will have few stalked
ciliates and  no other protozoa because  of  relatively few  bacteria, whereas, a somewhat less
stabilized system will have greater numbers of free-swimming ciliates because of greater numbers
of free-swimming bacteria. He stated that the presence of stalked ciliates indicates an activated
sludge system with a low BOD effluent. Vorticella was present in both reactors after  initial startup
except for one period in the 12.45 gal. reactor as described below.

After stable operation at temperatures <2° C and ^4° C the 12.45 gal. reactor temperature was
increased to 8°  C  over  a period  of  6 days. The effluent suspended solids  increased  from
approximately  5 mg/l before the  temperature  increase  to approximately  18 mg/1 during the
increase  and reached a maximum of 46 mg/1 after 3 days at 8° C. During this period, the effluent
became turbid with few solids settling out in the effluent tank. The protozoa became very reduced
in numbers and inactive. Again,  the return to normal operation corresponded to an increase in the
number of Vorticella and Paramecium  present in the sludge. Coliform removal also corresponded
directly to the numbers of protozoa  present, dropping from 99.8% removal before the upset to less
than 80% during the protozoa number reduction. Ten days after returning to  stable operation at
8° C, the sludge was exhibiting  the same  characteristics as with the 8.9 gal. reactor. That is, the

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222


SVI was ranging around 250 and the floe exhibited  a fluffy snowflake appearance. Operation of
the reactor was not impaired under these conditions because a backwash cycle was added to the
settling apparatus. Protozoa increased in numbers when the systems stabilized at 12° C.

Sludge wasting  and disposal  in cold climates should be given attention. Based on data presented
earlier, it would appear that provision should be made for wasting 0.5 Ib. solids per Ib. or BOD
removed at colder operating temperatures (<5°  C) and at organic loadings of 0.1 Ib. influent BOD
per Ib.  MLVSS-Day. Sludge  digestion  and disposal  methods present  a  problem at colder
temperatures due to  added heat requirements and poor drainability. Ludzack  (1965)  indicated
that sludge development at cold temperatures may require digestion at higher temperatures before
disposal.  Thomas (1950) indicated the freeze-thaw cycle may be taken advantage of in  cold
climates to increase drainability.

Tube  settlers have been evaluated as a  possible alternate means of providing solids separation and
return. During operation, sludge  rises in the tubes until it reaches a level at which it is in
equilibrium with the  effluent flow. Action in the tube consists of a rolling motion in which solids
are being carried up along the top side of the tube in a mass with the effluent, as shown in Figure
4. The mass gradually settles toward the bottom side of the tube where it enters a current moving
downward  caused by the weight of the  solids.  During normal operation, solids in the tube are
constantly  being replaced at a relatively high  rate. In the temperature range of 0° through 4° C the
SVI of the mixed liquor ranged around 230 and  did not hinder the operation of the reactor. At 8°

                                       TABLE  5

                         Summary of Results of 8.9 Gallon Reactor
                                    at 24-hr Detention

                               Feed: Primary Plant Effluent

                                            REACTOR TEMPERATURE (AVG°C)
                                            1.9            6.8           10.5

      Reactor MLSS (mg/1)                 2595          3872          3896
        %VSS                               83            83            82
        BOD                               1693          2105          1808
        COD                               3712          5019          5178
      i™Mr,a-    lb-Infl-BOD
      Loading.	_	            OQ7          OQ7          Q07
               lb MLVSS-Day

      Sludge Wasted:  	mg/MLVSS        0.42          0,16          „ 14
                     ing BOD Removed
      Unffltered Effluent
       Suspended Solids (mg/1)                 346
       BOD (mg/1)                           14            10            10
       BOD Removal (%)                     93            95            95
       COD (mg/1)                           51            53            69
       COD Removal (%)                     83            84            80
      BOD/COD Ratio
       Influent                            0.66          0.66          0.62
       Effluent                            0.27          0.19          0 13
       Reactor                            0.46          0.42          0.35

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                                                                                       223
                            Beginning
                            of clear
                            effluent and
                            sludge
                            interface
                                                           Clear
                                                           Effluent
                                                         Particles
                                                         rising above
                                                         sludge blanket
                                                     Sludge circulation
                                                     pattern
                   FIGURE 4   Sludge action in upflow clarifier settling tubes
C and above, the SVI  increased to values of 260 and greater and the sludge took on a fluffy
snowflake  appearance. The rolling  action of the sludge in the tubes stopped and the sludge height
began to rise, eventually spilling out with the effluent. Cutting the effluent flow rates back to less
than  0.2 gpm/ft2  resulted  in  lowering  the DO  in  the  effluent tubes to zero, which  further
complicated  the problem.  The  studies indicate that some  means for backflushing tube-settler
controlled  upflow clarifiers  must be provided  if mixed liquor concentrations greater than 2,000
mg/l are to be achieved with  reliable operation.

The 12.45 gal. reactor was operated for a period of time with a very low continuous overflow rate
and then increased to an  average  rate of 0.5 gpm/ft2 with  an alternating on-off cycle. In other
words, with the on 1/2 hour - off 1/2 hour cycle, the actual flow was 1 gpm/ft2 for 1/2 hour. The
SVI again ranged above 200 with very consistent solids removal. The effluent solids concentrations
were very low for the whole range of studies. The longer on times for the on-off cycle (2-1/2 hours
on as opposed to 1/2 hour) did indicate that longer cycles may result in higher effluent solids
concentration. Summaries of the results obtained at various  temperatures and  overflow rates are
presented  in Tables 6 and 7, and  Figures 5 and 6. Adding a backwash cycle provided  a definite
advantage in that it prevented a bulky sludge from becoming stagnant in the tubes.

Indications are that sludge bulking probably is a general problem in  the activated sludge process at
colder  operating temperatures and special  precautions  in  design will be necessary  to  assure
effective solids control. This problem was reported by Ludzack  (1965). Bulking sludges have not
been reported in cold temperature oxidation ditch studies (Anonymous,  1965; Grube and Murphy,
1968); however, these  ditches were operated at much longer detention times (1.6 to 2.3 days),
which may be a factor. Downing (1968) showed that settleability is improved by longer detention
time  |>10 hrs) and very short detention time (<5 hrs) when operating an activated sludge plant at
warm temperatures.  At any rate, indications  are that backwashing, in conjunction with lower
overflow rates, will  overcome this problem.

Pilot Plant

In cooperation with  the Alaskan Air Command,  the Alaska Water Laboratory constructed and
operated a pilot waste treatment facility  at Eielson Air Force Base (EAFB). The facility included

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     224
                                          TABLE 6

                           8.9 Gallon Reactor Results of Operation with
                       Varying Effluent Overflow Rates on the Settling Tubes

                 INFLUENT      REACTOR                   EFFLUENT

     Reactor1  Susp.               Susp.       Overflow  Susp.
      Temp   Solids BOD  COD  Solids        Rate    Solids  BOD  % BOD  COD   %COD
      (° C)   (mg/1) (mgA) (mg/1) (mgA) SVI  (gpm/ft2) (mg/1) (mg/1) Removal  (mgA) Removal
.35
'.7
(.4-.9)
4.2
(2.8-6.4)
3.8
(3.5-4.1)
95
112

94
77
244
253

193
142
292
370

229
283
3973 238
4237 238

4147 -
4067 229
.4
.3
.6
.3
.6
.5
.8
10
8
20
10
14
10
13
12
22
29
17
20
14
20
95
91
89
91
90
90
86
69
71
87
60
70
62
69
76
79
77
74
69
78
76
     (1)  Values in parenthesis are minimum and maximum for that period.
                                          TABLE 7


               12.45 Gallon Reactor Results of Operation with Varying Effluent Overflow
                                   Rates on the Settling Tubes

                INFLUENT          REACTOR                  EFFLUENT

 Reactor1  Susp.              Susp.       Overflow2          Susp.
  Temp  Solids BOD  COD Solids         Rate     Tube  Solids BOD  % BOD  COD   % COD
  (  C)  (mg/1) (mg/1) (mg/1) (mg/1)  SVI  (gpm/ft2)   Size  (mg/1) (mgA) Removed (mg/1) Removed

   2.4     77   177   303   3957   --      .2     2x3.5   2     19      89     35      88
 (1.4-3.5)                              (continuous)
                                                 4x3.5   2     19      89     39      87

   2.9     86   185   275   4157  214      .3     2x3.5   4     12      94     50      82
                                       (on 1/2 hr
                                       off 1/2 hr)  4x3.5   3     10      95     52      81

   4.4     93   223   321   4095  235      .5     2x3.5   4     12      95     55      83
 (4-0-4.7)                               (onl/2hr
                                       off 1/2 hr)  4 x 3.5   5     12      95     69      79

   7.8     87   194   313  4504  209      .5     2x3.5  12     20      90     69      78
 (6.8-8.4)                               (on 1/2 hr
                                       off 1/2 hr)  4x3.5  14     23      88     64      80

(1)  Values in parenthesis are minimum and maximum for that period

(2)  Notes in parenthesis indicate the time cycle of effluent flow through the tubes

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                                                                                        225
   50


   40-
•s

|  30

I

|  20"
_3


   10
                                      0
                                      A
                                                    MLSS'~4000mg/l
                                      a   *	3—t	7	
                                          Overflow Rate (gpm/ft*)
FIGURE 5  8.9 gal. reactor  sludge  heights  in  effluent tubes vs.  effluent overflow rates with
            continuous flow through tubes
                              20-
                            |
                                                         Umnd
                            f,
V
A O A
O
G V
contnuouc now
Ot rc
A»4*C
SVffT ft"
off 1/2 hr
D-rc
V-TC
Intftnnhtant Row
on Zhr
off llr
^~8«C
MLSS~400pmo/l
                                  .1  .2  .3 4  .5  Jj  7  A
                                    Owrflow RatM (gpm/ft2)

FIGURE 6  8.9 and 12.45 gal. reactors effluent suspended solids vs. overflow rates at various
            temperatures

an aerated lagoon and an extended  aeration basin. The purpose of the facility was to increase the
knowledge of biological waste treatment at cold temperatures and to develop design criteria.

Eielson Air Force Base is located 22 miles southeast of Fairbanks. The mean annual temperature at
Fairbanks is  approximately 25° F with minimum and maximum recorded temperatures of -66° F
and +99° F  respectively  (Johnson  and  Hartman, 1969). The  area has approximately 150 days
below 0° F.
Originally intended to serve as, a facultative lagoon, the extended aeration unit consisted of an
earthen basin lined with 20 mil polyvinyl chloride film (PVC) and tube settler modules as shown in
Figures 7 and 8. The PVC film at the bottom of the basin was covered with 6 inches of sand and a
concrete pad poured in the center for support of aerators. Aeration and mixing were provided by

-------
 226


 eight Hydroshear aerators, manufactured by the Chicago Pump Company. Air supply was by a 120
 SCFM Sutorbilt blower, manufactured by the Fuller Company.

 Solids separation was provided by two tube settler modules. The tube settlers were developed by
 Neptune Microfloc Company for use in water treatment. The manufacturer has recently initiated
 studies to adapt them for use in activated sludge separation (Hansen, Culp and Stukenberg, 1967).
 This type of settler was felt to provide optimum design for submerged operation which was desired
 to overcome icing problems. The basin was fed by a Mar low centrigal pump, manufactured by ITT
 Marlow Company. Pumping rate was approximately 180 gpm with the feed drawn from a manhole
 on the influent line just before entry to the EAFB primary treatment plant. Temperature of the
 sewage averages about 20° C with the sewer lines enclosed in a utilidor, which is heated during the
 winter months.

 The extended  aeration facility was built to provide the very simplest operation with a minimum of
 environmental  protection  for  evaluation  under  cold climate conditions. Construction of the
 extended aeration facility was completed in December 1968 and the unit placed in operation later
 that month. The unit was operated at a 2-day detention  time, which corresponded to an average
 overflow loading rate on  the  tube settler of 1.3 gpm/ft2. A problem  was encountered with
 breakage of pumps due to entrained solids entering the pumping chamber. The feed line also filled
 with solid material and plugged. As a result, the basin was not fed for a week, during which time 3
 feet of ice formed over the pond and frozen foam built up to 8 feet above the aerator.

 Beginning in January 1969 and lasting approximately 6 weeks, a period of extremely cold weather
 occurred with  ambient air temperatures dropping as low as -60° F. A detention time of 1 day was
 maintained during  this  period with  no  ice forming.  The loading  on  the tube settlers  was
 approximately 2.5 gpm/ft2. The gear housing of a compressor was broken and teeth stripped from
 the gears while attempting  to  start it at a low temperature. Apparently, metal contraction had
 reduced clearances which caused internal rotating parts to make contact with and break the pump
 housing.

 During February, the feed pumps were moved inside the Eielson primary treatment plant and feed
 taken from the grit chamber.  For the  remainder of the winter and the following spring, while
 operating at a detention time of 2 days, the MLVSS of the system generally did not rise above 500
 mg/l.

 Inadequate  mixing was suspected as the cause of poor performance, and velocity measurements
 were made  with an ice current meter  obtained from the U. S. Geological Survey which measured
 the horizontal  component  only.  Velocities  were generally lower than the 1.0  ft  per  second
 recommended for complete  mixing, except within 2 feet of the surface. The aeration rate was 120
 cfm, depth of the basin 11 feet, with approximately 4 horsepower input. Velocities were measured
 again at a later date with 300 cfm being delivered and 9 horsepower input with generally the same
 results  except  the surface velocities were  higher.  The velocities found were not considered low
 enough to cause the extremely poor basin performance.

The possibility  of excessive turbulence  being carried into the tubes was also considered because of
the close proximity of the settler modules to the  aerators (2-3 feet). To check the possibility,  a
new aerator  was fashioned of a  short length of 3-inch pipe attached to flexible hose and placed in
the basin approximately  10 feet from the  settler modules. The MLSS of the basin increased to

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                                                                                        227
                                              Plan Vbw
                                           Maximum Woridng Liqw) Depth

                                             View A-A
           FIGURE 7   Extended aeration pilot facility, Eielson AFB (1968 configuration)
                                                          Effluent
                                                          Header
                      FIGURE 8   Tube settler module (1968 configuration)

1,000 mg/l during operation of this aerator which did indicate that basin turbulence or entrained
air bubbles was affecting the settler operation.

The  basin was then taken  out of operation to permit modifications in preparation for the next
winter's operation. The modifications are illustrated in Figures 9 and 10. The system was placed in
operation in December 1969.  It was recognized that at a detention time of 24 hours and with low
winter operating temperatures, the hydraulic load on the tube settlers would be too great. An
attempt was made to reduce  the hydraulic  load on  the system while it maintained a BOD load
equivalent to a 24-hour detention  time system by supplementing  the feed with primary sludge
from the Eielson treatment plant. Basin velocity proved to be restricted around and beneath the

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228
                                         /Cttieaao Pump
                                         (ShcorfuHTS

                                         kTS.
                                         Plan View
                                        Elevation
 FIGURE 9  Extended  aeration  pilot  facility  after modification,  Eielson  AFB  (1968

           configuration)
              0 •••
               ••••
               •• .
               eo»*
               00 »•

               «•••«
               •••°
                «••
               o o
                « •«
                o*«
               OQOO
o»»   .    ^
>0»0   /    .-




g^/
•t*    '
          X  /


           /   '
                •Ji
                *v
 l^   ^
                 MO

                 0»*
                 \\\\\\\\\\\\\\\\\\\\\
FIGURE 10 Tube  settler  beneath  module design  with  flow  beneath  the  hopper (1969

           configuration)

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                                                                                        229
separator hoppers because of the low clearance and resistence offered by the settler support. As a
result, a heavy sludge deposit blocked the separator hoppers, accumulated in the tubes and passed
into the effluent.

During a cold period in January 1970, the surface of the basin began to freeze due to tow heat
energy  being supplied. The  sludge accumulated in the ice,  reducing the suspended  solids level in
the pond from approximately  2,500 mg/l to  less than  200 mg/l. During this period, the mean
ambient temperatures averaged -23° F, with a range of -8
knots to calm and averaged 3 knots.
'° to -35° F. Wind velocity ranged from 10
A block was cut from the ice and a sample taken of the unfrozen sludge beneath the ice. A cross
section is shown in Figure 11. The ice had reached  a thickness of 14 inches with a sludge layer of
17 inches beneath the sampling point. The sludge was not moving under the ice and apparently
had attached itself, building up a thicker and  thicker layer which eventually froze into the ice
layer.
                                                 Sample
                                                location
                                 Aeration Basin

3"


r"
I
Relatively Clear

12,000 mg/l
18,000 mg/l
30,000 mg/l

T
Ice
Layer

\
I4.0OO mg/l


Sludge
Layer

                                               MLSS before ice build-up= 2500mg/l
                                               MLSS after ice build-up  =  400mg/l
                                               Hydraulic detention time'   4 days
                                               Average air temperature    -23°F
                                                            Maximum     -8°F
                                                            Minimum'    -35° F
                                               Avg. wind during freezeup=   3 knots
                                                            Maximum1   10 knots
                                                            Minimum-'     Calm
       FIGURE 11 Profile of surface ice and sludge layers of frozen extended aeration basin

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230


The long sloping side walls associated with earthen basins present two very important problems in
activated sludge aeration  chamber  applications. The  relatively high surface area-to-volume ratio
will result in high heat energy  losses from  the  system which may be very critical with low
temperature  influent. Greater  heat losses will promote  ice formation which  will entrain  MLSS
from the system, destroying the effectiveness of the process.

The second problem is the difficulty in obtaining adequate basin velocities at lower depths without
excessively high horsepower for mixing. Even at high aeration rates, the minimum recommended
velocities of  1.0 fps were generally not present  in the  pilot facility extended aeration basin at
Eielson Air Force Base.

Another effect observed  during  operation in the second winter was that, with the aerators off
center, a circular flow was induced in the basin in the horizontal plane around the aerators. The
flow was similar to the Coriolis effect and seemed to be promoted by the earthen basin shape of a
large  surface area-to-bottom area ratio. This  effect will only become a problem in situations in
which flow directions in  the basin are important, as in the Eielson AFB  pilot facility, where the
circular flow pattern did have an effect in hindering sludge removal from beneath the hoppers.

The cross sectional  shape of a basin and the  temperature to which it is exposed will, in general,
determine the type  of liner which  should be  provided. Material must be  used  which will prevent
erosion and scouring by velocities in the basin. Side slopes of less than 1  vertical to 2 horizontal
permit use of flexible liners,  whereas vertical sides  will  require  bearing wall construction  of
impermeable concrete or wood crib design with an impermeable liner.

Experience with the PVC  liner indicates it is not feasible for use in permanent installations for cold
temperature  applications. The  liner  becomes very susceptible to damage  at low temperatures
because of brittleness, and  ice  formation  can cause extensive breaks in the lining. Aging and
exposure to sunlight also increase its susceptibility to damage.

Impermeable liners  such  as low temperature butyl  rubber membranes  are  feasible for  use in
earthen basins when  the danger of major freezing does not exist. Care must be taken to insure that
the  liner  is resistant to  hydrocarbons which  may  be present in the  sewage as softening  or
dissolution may result.

Concrete provides a reliable material for cold temperature application. However, construction is
expensive  in Alaska  and particularly so in remote areas.  Examples of the successful application of
cheaper methods of  concrete construction are the College Utilities oxidation ditch in Fairbanks,
Alaska, and the oxidation ditch at Glenwood, Minnesota (Anonymous, 1965). Concrete block was
used for the construction of vertical sides for the College Utilities ditch. Concrete silo staves were
originally used for the sloping sidewall construction  of the Glenwood ditch but were not  sealed
and soil behind  the  staves washed out. The problem was  successfully alleviated by placing steel
mesh and 4 inches of concrete grout over the staves to  provide a smoother waterproof lining.

                                      CONCLUSIONS

The feasibility of the extended  aeration activated sludge  process as  a relatively economical and
effective means of secondary waste treatment has been demonstrated in the laboratory and in the
field.  The  process requires more consistent operation and maintenance than aerated lagoons and
this is a disadvantage where costs are high and skilled operators are extremely scarce.

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                                                                                       231


The utilization of exposed aeration chambers for the extended aeration process is feasible. Earthen
basins  are  also  feasible for use where economic and  construction  conditions warrant. When
utilizing exposed basins, heat loss effects must be evaluated  in conjunction with detention time
determinations to avoid potential freezing problems. Solids entrainment in ice can cause failure of
an activated sludge process.

Environmental  protection  in varying degrees should be provided for the remaining equipment,
such as heated enclosures for pumps and flow measurement devices. Housing must be provided for
secondary  sedimentation  basins and should include a minimum  of an unheated structure with
panels which can be removed for warm weather operation.

Effective solids separation  is the key to successful  operation of extended aeration facilities and is
dependent  on both the biological and physical aspects of the system. It has been demonstrated
that a  sludge can be developed which will perform very efficiently at temperatures less than 1° C.

A turbid effluent will result at cold temperatures with an unacclimated sludge or loading rates that
are too high. Under these conditions, a  less stabilized sludge develops with a corresponding relative
decrease  in numbers of stalked ciliates and an increase of  dispersed bacteria which appears to
contribute to turbidity (McKinney and Gram, 1956).

A bulking sludge may develop  at cold operating  temperatures. This type of sludge can lead to
separation  problems but will  provide a very clear effluent at temperatures ranging down to less
than1°C.

Properly designed tube settlers will provide effective cold (0 to 4° C) temperature solid separation.
This is true for sludges with SVI's  ranging up to 250. A  backwash cycle  should be provided for
reliable operation and is mandatory  for operation with high MLSS concentration (4,000 mg/l) and
bulking sludges. Some effort should be directed toward developing upflow clarifier configurations
for cold temperature application since  the method has advantages (Reed and Murphy, 1969). The
tube  settler does provide an upflow  clarifier type action  in high MLSS activated sludge  solid
separation  applications. Providing  consistent solids  separation  with tube  settlers  at  warmer
temperatures (greater than 4° C) appears to be the most demanding and yet insufficiently defined
area of need in their application.

Cold  climate sludge wasting and  disposal for the  extended  aeration process must be given
consideration for the following reasons:

     1.   Excess solids production increases with decreasing temperature.

     2.   Shorter detention times to prevent freezing will also increase solids production at a given
          MLSS level.

     3.   Auto-induced  sludge  wasting  may be  expected   to be  more  severe, placing greater
          potential stress on the receiving water.

     4.    Retarded assimilative capabilities of the receiving water at cold temperatures.

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232


                                  RECOMMENDATIONS

Facility Design

The following design recommendations  are  based  on laboratory  studies,  experience  with the
Eielson Air Force Base pilot facility, and experience reported by others:

(1)  Exposed  aeration  basins should  be considered  for  reducing construction costs  of  waste
treatment facilities. Raw sewage temperatures and heat loss effects must be considered to prevent
freezing which can cause process failure by entrainment of solids from the system.

(2)  Housing  should  be provided for pretreatment units  such  as bar  racks, pumps and  flow
measuring equipment.

(3)  Some minimum protection should be provided for aeration equipment such as strip heaters or
minimum heat enclosures for compressors and untreated housing for oxidation ditch rotors.

(4)  Housing should be provided for secondary sedimentation basins.  Minimum housing would
include a structure with panels which may be removed for warm weather operation.

(5)  Where  economic and  construction considerations warrant, earthen basin designs should be
considered for aeration chamber construction.  Otherwise, sidewalls that are vertical or  nearly so
should be utilized to promote better mixing.

(6)  Submerged  settling units should be situated in  the center of  basins with low sidewall
construction with aeration on at least two sides to promote adequate mixing. Several questions
require answers before submerged settling units are practical.

(7)  When basins with low sidewall slope construction are utilized without submerged settling
units, the aeration devices should be clustered in the  center of the  basin for best mixing.

(8)  Flexible membranes should not be used where the danger of heavy icing exists.

(9)  Concrete block and concrete grout should be considered as economical liner materials where
the design permits.

(10)  Tube settlers with backwashing of  tubes should be considered. However, more information
is necessary before their reliability can be ascertained. Both routine and emergency maintenance
must be carefully evaluated prior to their  use.

Process Design

The following preliminary  recommendations for low temperature extended aeration  systems are
based on laboratory studies and experience reported by other investigators. Attempts will be made
to verify these findings on a pilot plant scale.

(1)  Organic loadings should be maintained below 0.20 Ib. BOD/lb. MLVSS-Day.

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                                                                                        233


(2)  Provision should be made for sludge wasting of 0.5 Ib. MLSS/lb. BOD removed, particularly
at shorter detention times such as a 12-hour detention time system.

(3)  Tube  settler overflow rates should be held below 0.5 gpm/ft2 with high MLSS concentrations
{> 4.000 mg/l).

(4)  Sludge wasting and disposal facilities or a polishing lagoon for effluent discharge should be
provided where heavy discharges  of suspended  solids  may  place  excessive stress  on receiving
waters.

Research and Development Needs

The following list of suggested research and development needs is not intended to be all inclusive
but  includes areas which have come  to the attention of the authors through laboratory and pilot
plant experience and a review of experience reported by other investigators:

(1)  Sludge bulking conditions at lower temperatures (8° C and below)  must be defined so the
condition can be predicted in actual application.

(2)  Further develop low temperature biokinetic parameters at detention  times ranging from 4 to
36 hours with varying MLSS levels.

(3)  Further develop low  temperature tube settler design criteria and backwashing techniques at
various MLSS levels.

(4)  Investigate upf low clarifier designs for low temperature application.

(5)  Investigate methods  of sludge  digestion and disposal  under  low temperature conditions;
particularly the use of the freeze-thaw cycle as an aid to promoting better drainability.

(6)  Develop reliable methods for positive recirculation of settled solids from submerged settling
units.

(7)  Further investigate criteria for predicting heat loss from exposed basins.

(8)  Continue  evaluation of  cold temperature biokinetic design  parameters on pilot  plants and
existing facilities.

(9)  Develop design and operation criteria for low temperature horizontal flow clarifiers.

(10)  Investigate  power  requirements  and   mixing  characteristics  of  various earthen   basin
configurations.
      Further investigate the effects of heavy ice cover on solids entrapment in aeration basins,
 particularly where flow patterns are parallel to the surface as in the oxidation ditch.

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 234
                                     REFERENCES
Anonymous (1961)  Effect of  water  temperature  on stream  reaeration, Thirty-Fjrst Progress
     Report, Committee on Sanitary Engineering Research, J. of San. Eng. Div., Proc. Amer. Soc.
     of Civil Engineers. 87, No. SAG.

Anonymous (1965) Report on operation of oxidation ditch sewage treatment plant, Glenwood,
     Minnesota, Dept. of Health, Div. of Environ. Health, Section of Water Poll. Cont.

Ayres, J.  C.  (1962)  Temperature and moisture requirements, Low Temperature Microbiology
     Symposium Proceedings (Camden), Campbell Soup Company.

Benedict,  A. H. (1968)  Organic  loading  and temperature in  bio-oxidation, Ph.D. Thesis, U. of
     Washington.

Black, S. A. (1968) How to evaluate aeration devices. Water and Pollution Control, 106, No. 10.

Culp, G. (1969) A better settling basin, The American City.

Downing.  A. L. (1968) Factors to be considered in the design of activated sludge plants. Advances
     in Water Quality Improvement, U. of Texas Press, pp. 190-202.

Eckenfelder, W., Jr.  (1967) Theory of biological treatment of trade wastes, J. Water Poll. Cont.
     Fed., 39, No. 2.

Eckenfelder, W. W. and O'Connor. D. J. (1961) Biological Waste Treatment, Pergamon Press, Inc.,
     Long Island, New York.

Frey,  P.  J. (1969) Significance  of winter  dissolved oxygen  in Alaska, presented Alaska Water
     Management Association Annual Meeting.

FWPCA Methods for  Chemical Analysis of Water and Wastes,  Fed. Water Poll. Cont. Admin., Div.
     of Water Quality Research, Analytical Quality Cont. Lab., Cincinnati, Ohio.

Gordon, R. C. (1970) Unpublished data, Alaska Water Lab., College, Alaska.

Grube, G. A. and Murphy, R. S. (1968) Oxidation ditch works well in sub-arctic climate. Water
     and Sewage Works, 116, No. 7.

Gustaffson, B. and Westberg, N. (1965) Experiment with treatment of sewage from the town of
     Kiruna by the activated sludge method. Royal Inst. of Tech., Stockholm, Sweden, Inst. of
     Water Supply and Sewage Tech., Inst. of Water Chem., 65, No. 4.

Halvorson, H. O.. Wolf, J. and Sunevasan, V. L. (1962)  Initiation of growth at low temperatures,
     Low Temperature Microbiology Symposium Proceedings (Camden), Campbell Soup Co.

Hansen, S. P. and Culp, G. L. (1967)  Applying shallow depth sedimentation theory, J. Amer.
     Water Works Assoc., 59, No. 9.

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                                                                                     235


Hansen,  S.  P.,  Gulp.  G. L.  and Stukenberg, J. R. (1967)  Practical  application  of  idealized
    sedimentation theory. Presented 1967 Water Poll. Cont. Fed. Conf., New York City.

Heukelekian, H. and Wiesburg, D. (1965) Bound water and activated sludge bulking. Sewage and
    Industrial Wastes, 28, No. 4, p. 558.

Hunter, T.  V.,  Genetelli, E.  J. and  Gilwood, M.  E. (1966) Temperature  and retention  time
    relationships  in  the activated   sludge  process, Proc.  21st Indust.  Waste Conf., Purdue
    University.

Johnson, P. R.  and Hartman, C. W. (1969) Environmental Atlas of Alaska, Inst. of Arctic Environ.
    Eng., Inst. of Water Resources, U. of Alaska, College, Alaska.

Ludzack, R. J.  (1965) Observations on bench scale extended  aeration sewage treatment, J. Water
    Poll. Cont. Fed.. 37, No. 8.

McKinney,  R.  E.  and Gram, A. (1956)  Protozoa  and activated sludge, Sewage and Industrial
    Wastes, 28, No. 10.

Miller, A.  P. (1967)  The biochemical basis of  psychrophily  in microorganisms, Inst.  of Water
    Resources, U. of Alaska, College, Alaska.

Pasveer, A.  (1955) Research on activated sludge, V: rate of  biochemical oxidation, Sewage and
    Industrial Wastes, 27, No. 7.

Pohl, E. F. (1967) The effect of low temperatures  on aerobic  waste treatment processes, M.S.
    Thesis, U.  of Washington, Seattle, Washington.

Pohl, E.  F.  (1970) Chief, Personal Communications,  San. Eng. Sec., District  Engineers Off., U.S.
    Army Corps of Eng., Anchorage, Alaska.

Reed,  S. C. and Murphy, R. S. (1969) Low temperature activated sludge settling, J. of the San.
    Eng. Div.,  Proc. Amer. Soc. of Civil Engineers, 95, No. SA4.

Roguski, E., Personal Communications, Alaska Department of Fish & Game, Fairbanks, Alaska.

Schlecta, A. F. and Hsiung, K-Y (1969)  High rate processes in advanced waste  water treatment.
    Presented  1969 Water Cont. Assoc. Pennsylvania.

Schmidtke, N.  W. (1967) Low temperature oxidation ditch field study, Thesis  to Dept. of Civil
    Engineering, U. of Alberta, Edmonton, Alberta, Canada.

Standard Methods for the Examination of Water and Wastewater, 12th Edition, Amer. Pub. Health
    Assoc., New York.

Stewart, M. J.  (1964) Activated sludge  process  variations -  the  complete spectrum. Water and
    Sewage Works, pp. R2-41 - R2 62.

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236


Thomas, H. A., Jr. (1950)  Report of investigation of sewage treatment in low temperature areas,
     for the Sub-Committee Waste Disposal, Comm. on San. Eng. and Environ., Nat. Res. Council.

Wuhrmann, K.'(1956) Factors affecting efficiency and solids production in the activated sludge
     process,  Biological  Treatment of Sewage  and  Industrial Wastes. B. J. McCabe  and W. W.
     Eckenfelder (ed), Reinhold Publishing Company, New York, New York.

Zanoni, A.E. (1969) Secondary effluent deoxygenation at different temperatures, J.  Water Foil.
     Cont. Fed., 41 .No. 4.

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             CHEMICAL TREATMENT  OF MECHANICALLY  AND
                   BIOLOGICALLY  TREATED WASTEWATER
                                     Arne Rosendahl

                                    INTRODUCTION

Eutrophication problems are found to be serious in many Norwegian lakes and fjords.

An  extensive survey of the pollution  in the  inner Oslofjord  has shown that organic matter
produced by autotrophic growth,  mostly  due to the discharge of nutrients, is 10 - 12 times the
primary organic load from wastewater. In  this stratified, landlocked fjord, with a brackish surface
water, the nutrients found to be most important are phosphorus, nitrogen, and iron. With the large
amounts of nitrogen and iron naturally being brought into the system, phosphorus is at the present
the only controllable component.

The same reasoning is found applicable to most of our eutrophied waters, and numerous treatment
plants for removal of phosphorus from wastewaters will have to be installed in years to come.

Today phosphorus removal is thought to be most economical by chemical coagulation/floccutation
and with sedimentation or flotation for the liquid/solid separation.

Several people have studied  the theoretical basis for such chemical processes (Stumm and Morgan,
1962; Stumm, 1962; Pope I,  1966;  Henriksen, 1962; and Henriksen, 1963}  but there is still a lack
of some essential knowledge. This  makes it difficult to make a process design on a purely rational
basis, and the  treatment plants now in operation are  therefore designed  on experience gained
through chemical treatment of drinking water during many years, and through experiments made
in new plants for phosphorus removal (Wuhrmann, 1964).

The great majority of these plants are built as tertiary units, i.e. chemical treatment of biologically
treated waste. At a few plants chemical and biological treatment take place simultaneously in the
same reactor (Thomas, 1962).

In Norway there are only a  few biological treatment  plants, and we have therefore been looking
for a more direct way of phosphorus removal by omitting  the biological unit. During 1967 some
treatment plants were  built in Sweden  using mechanical/chemical treatment, but systematic
observational data describing the process was limited.

Pilot plant  studies were needed  giving comparable results between  mechanical/chemical and
biological/chemical  treatment  systems, and  results and experience that could be translated to
full-scale  treatment plants.  In  1968 a study'was  started  at the Norwegian Institute for Water
Research, and results from V/2 years' program are reported in this paper.
                                          237

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238


                         DESCRIPTION OF THE  PILOT PLANTS

Five pilot plants were used for  this investigation. They were situated at the site of a biological
treatment plant owned by the city of Oslo, treating the effluent of about 50,000 inhabitants, using
the conventional activated sludge method.

One extended aeration plant, type Hycon 5 A, previously used by this institute to study kinetics
of biochemical treatment, was reconstructed. This plant was divided on four parallels based on
coagulation/flocculation and sludge removal by sedimentation (Fig. 1). A fifth separate plant used
coagulation/flocculation and sludge removal by flotation (Fig. 2).

All five  plants were  in use from January  1969 until May 4, 1970. On that day a serious fire
stopped the experiments at the four sedimentation plants.

Each plant consisted of:

     1.   Wastewater intake arrangement

     2.   Chemical feeding equipment

     3.   Rapid mixing

     4.   Flocculation basins

     5.   Sludge-separation equipment (sedimentation or flotation)

     6.   pH recorder

     7.   Sampling equipment

Sedimentation Plants

During this investigation primary treated wastewater was used in two plants and secondary treated
wastewater was used in the two other plants.

During the first investigation period a technical quality of aluminum sulfate, type AVR from
Boliden i Sweden, was used. (This type of alum has about 2% impurities, mainly iron and silicates.
It is produced for chemical treatment of  sewage and  is at the moment the  cheapest  alum in
Scandinavia).  In the  last  part of the investigation period sulfuric acid was dosed in addition to
alum, for pH adjustments. Both  alum and  sulfuric acid were made up to a 5% solution. The
chemicals were  added to the wastewater ahead of the flocculation basin. To obtain sufficient
mixing the chemicals were added where the water was quite turbulent.

The flocculation basin had four treatment plant paddles mounted on horizontal parallel axes. They
were driven by the same motor, and ran at the same speed. The speed, however, could be varied
within a wide range. Each flocculation basin was 2.5 m long, 0.6 m wide and 0.8 m deep, and was
divided into three  chambers by vertical walls with a 30 cm hole around the paddle axes to prevent
short circuiting. Periphery velocity was selected as 0.4 m/sec. This gives theoretically  calculated

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                                                                                                      239
         Paddle
 Section B, - 6,
                                    Paddle
                             Section B, — Bj
                                                                Paddle
                                                        Section B3 - B3
1  Dosing pump
   main chemical

1  Dosing pump
   •ck) or coagu-
   lation aid

3  Motor for paddles

4  Sludge removal
   pump

5  Sampling pump

6  Refrigi rater
   for samples

7  Automatic instru-
   mentation for
   sludge removal

8  pH-instruments

x  pH-electrodes

.  Sampling points
                 Chambers for
                 water distri-
Holding tanks  I   butionand
for chemicals  I   quantity
                 control
                    Biologically treated  influent!
                - Mechanically treated  influent' Surplus water and
                                               sludge effluent
Holding tanks
for chemicals
                                          Distribution
                                          chambers
                                           H.AN
                                                             Flocculation unit
                                                                                       Sedimentation unit
                                                                                        Sampling
                                                                                              Effluent
    Section A — A
                  FIGURE 1    Sedimentation plants

-------
240
 1   Influent

 2   4 rapid mix chamber

 3    Rapid mixer for scum-control

 4    First flocculation compartment

  5   Second f tocculatkm compartment

  6   Paddle with motor        A

  7   Flotation unit

  8  Shut off valve for effluent

  9   Effluent

  10   Sludge outlet

  11   High pressure 1>ump

  12   Level regulate*

  13   Pressure tank

  14   Compressor
Qlm
                         0,1m
                                                             0,7"
                                   PLAN
   IS   Rotameter

   16   Reduction v*lve for dispersion

   17   Holding unk* for main chemical

   18   Dosing pump tor 17

   19   Motor»ndpaddle forchemical
        holding tanks

   20   Holding tank for acid or
        coagulation aid

   21   Dosing pump for 20

   22   Sampling pump

   23   Refrigirator for samples

   24   Sampling point

   25   pH-inctrument

   26   pH-electrode

   27   Motor for sludge scraper

   28   Sludgescraper
                                                                                                ,15m       O.7n
SectionA-A
                                                                              This equipment is placed
                                                                              on the tame level in
                                                                              front of the flocculdtion
                                                                              compartments
                                                          FIGURE 2    Flotation plant

-------
                                                                                      241


g-values of 59 sec"1. 55 sec"1 and 46 sec"1  in the first, second and third chambers (Camp. 1943).
The  influence of g-value  variation at the plant has been studied as a diploma thesis for Civil
Engineering in the autumn 1969.

The sedimentation units each had a length of 2.5 m. the width being 0.6 m. The bottom had steep
slopes to the  middle and  the deepest point was 2.7 m below the surface. Water entered the basin
from one end, flowing about horizontally through the basin and leaving at the other end  over a
V-notch weir. Sludge was withdrawn automatically for 30 seconds every hour.

Equipment for pH recording was installed in autumn 1969, and pH values were recorded on both
mechanically  and  biologically  treated  wastewater  before  adding chemicals, and  in the first
flocculation chamber of each plant. Sampling was done continuously during every 24 hour period,
and the bottles placed in a refrigerator.

The  hydraulic load was 1.2 m3/hr (5.28 gal/min) to each unit. This load was selected after trial
runs with varying loads. Sludge loss from the sedimentation units was kept at a practical level. This
toad gave a theoretical detention time  of  1  hr  in the flocculation units, about 1.5 hr detention
time, and theoretical overflow rate of 0.8 m/hr (470 GPD/Sq Ft) in the sedimentation  units.

The Flotation Plant

Primary effluent was  treated in the fifth plant  throughout the whole investigation  period. 10%
solution alum as well as sutfuric acid was used.

The chemicals used were mixed with the wastewater in a baffled rapid mixing basin. The plant was
provided with two flocculation chambers coupled in series, with separate paddles on vertical axes.
Each flocculation chamber had an  area of 0.7 x  0.7  m and a depth of 1.06 m. Paddles ran with a
peripherical speed of 58.5 cm/sec in the first chamber and 35 cm/sec in the second chamber. This
gave theoretical g-values of 78 sec"1 and 37 sec"1  in the first and the second chamber.

The flotation unit itself was circular with a diameter of 97 cm  and a depth  of 37.5 cm, made of
concentric cylinders and cones. Flotation was effected by small air bubbles. They were produced
by solute air in  water under 5  atm.  pressure. The  pressure was released just before adding  the
flotation medium to the flocculated wastewater.

The  sludge floated at the surface while the water flowed downwards and left the unit through four
pipes at the  periphery. The four pipes were connected to a larger pipe. The water level in the unit
was controlled at the outlet. About 15% of the effluent was used to make up the dispersion water.
This quantity was manually controlled by a flowmeter.

Sludge withdrawal was automatically" controlled by a timer. Sludge was removed  by closing  the
outlet  valve for approximately 2 minutes every hour. While the water level increased, sludge and
water left the plant over a mechanically cleaned weir.

The flotation plant was designed for 2 m3/hr (8.8 gal/min)  loading. This hydraulic load was kept
constant throughout the  test period. This gave a total theoretical detention time of 31 minutes in
the flocculation  chambers. Theoretical detention  time in the flotation chamber was  5.1 minutes
with the overflow rate of 4.3 m/hr (2520 GPD/Sq Ft). The plant had a pH recorder. Composite

-------
242


sampling was done during the complete test. Samples of  the  raw wastewater  entering the
community plant were also analyzed.


                              ANALYZED PARAMETERS


Several parameters  were considered for the evaluation of the quality of the influent, effluent and
kinetics of the processes.


The following parameters were analyzed:


     Organic matter:  chemical oxygen demand (COD) by the dichromate method


     Biochemical oxygen demand, seven days test (BOD7)


     Total phosphorus, orthophosphate


     Nitrogen:  Kjeldahl and the sum of nitrite-nitrate nitrogen.


     Turbidity (JTU)


     pH, continuously  recorded in flocculation chamber, and measured on day-samples  in the
     laboratory.


     Aluminum



                                      TABLE 1


                             Mechanical/Chemical Treatment

                           Sludge Separation by Sedimentation

                                 Chemical Dosed: Alum
Water *  Chemical dose
quality    alum mg/1

  R
  M
 M/C        75

  R
  M
 M/C        100

  R
  M
 M/C        125

  R
  M
 M/C        150
                                                           Parameters

                        No. of day      COD
mples
re. value
4
4
4
8
6
5
4
4
4
8
6
5
(K2Cr,07)
mgO/1
186.4
166.6
91.1
158.6
104.3
59.0
186.4
166.6
42.1
158.6
104.0
44.0
BODj
mgO/1
94.5
48.0
35.0
98.0
49.6
18.3
94.5
48.0
10.5
98.0
49.6
17.5
Tot.P
mgP/1
4.65
4.58
3.75
4.45
4.13
1.61
4.65
4.57
0.14
4.45
4.13
0.14
Kjeldahl N
mgN/1
19.2
20.9
17.5
17.3
19.2
13.2
19.2
20.9
17.6
17.3
19.2
14.3
Turb.
JTU
61.0
28.5
15.8
51.8
14.6
10.8
61.0
28.5
1.5
51.9
14.6
0.9
pH
7.30
7.11
7.12
7.56
7.39
6.86
7.30
7.11
6.74
7.56
7.39
6.42

-------
                                                                                     243
Calcium, magnesium and alkalinity were  measured on a series of samples to obtain the average
hardness of the treated water.


The process  variables  selected were  chemical dosage,  hydraulic loading and flocculator speed
(g-values).


                         RESEARCH PROGRAM AND  RESULTS


The first research series covered doses of 75, 100, 125 and 150 mg/l alum. These doses were added
to biologically treated wastewater and mechanically treated wastewater.


The results are given in Tables 1, 2 and 3, and some results are shown graphically in Figure 3.


During these experiments it was obvious that quality of the effluent varied extremely during the
day. The results seemed  to follow the variations of pH which could vary within ± 1.0 pH unit
during the day, with the lowest pH at 6:00 a.m. and the highest value about 1:00 p.m. Turbid and
colored effluent was noticed when the pH was higher than 6.2 - 6.5 in the flocculation chamber. It

looked as  if a critical pH value was lower at a lower dose of alum. From this it was decided to try
alum doses of 70, 80, 90 and 100 mg/l and adjust pH to a maximum of 6.5 using sulfuric acid. The
results of these experiments are listed in Table 4 and some results are shown graphically in Figure
4.

                                        TABLE 2


                              Mechanical/Chemical Treatment

                                Sludge Removal by Flotation
                                  Chemical Dosed:  Alum
                                                               Parameters
 Water*
 quality

   R
   M
  M/C

   R
   M
  M/C

   R
   M
  M/C

   R
   M
  M/C
Chemical dose
alum mg/l
75
100
125
150
No. of day
samples
for ave. value
10
8
10
4
4
4
8
9
9
7
5
7
                                         COD
mg
   ro
   O/1
231.4
149.0
 92.4

137.5
101.4
 45.8

209.1
123.9
 47.4

194.3
109.5
 34.4
 BODj
mgO/1

 122.0
 58.4
 25.8

 83.5
 47.0
 14.8

 114.0
 47.0
 10.9

 132.8
 40.3
  8.7
 Tot.P
mgP/1

 5.04
 4.63
 2.84

 4.43
 3.98
 0.99

 5.88
 4.53
 0.32

 4.68
 4.38
 0.19
Kjeldahl N
 mgN/1

  21.5
  20.9
  19.2

  16.9
  19.7
  15.2

  28.1
  20.2
  19.9

  19.5
  17.5
  15.6
Turb.
JTU

96.1
26.6
20.0

29.9
13.3
 5.6

34.0
16.2
 1.1

62.4
15.9
 1.3
 pH

7.23
7.05
7.07

7.54
7.44
7.04

7.50
7.27
7.02

7.46
7.14
6.61
 R =  Raw wastewater
 M =  Mechanically treated
 B =  Biologically treated
 C =  Chemically treated

-------
244








in —

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Mean values:
Raw sewage 203.
Mechanically treated 125.
Biologically treated 53.



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                                       75          100

                                             Alum-dose mg/l
                                                              125
                                                                         150
                                                       Mean values:


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Rawsewa
Mechanic
Biologica
•N^
^-^.
' 	 	
1
ge 111.9mgO/t
ally treated 49.4 mg O/l
ly treated 1 0.4 mg 0/1


u
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1
                                       75         100

                                             Alum-dose mg/l
                                                              125
                                                                         ISO

CL
1
5
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Mechanic
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ally treated 4.44
Biologically treated 3.86


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5 100 125 150
                                             Alum-dose mg/l
                               Symbols:
                                          meal treatment  "I Sllia^ removai by sedimentation
                                          imical treatment J
                            A Mechanical-chemical treatment   Sludge removal by flotation


FIGURE 3   Results by  dose  of alum at sedimentation  and flotation  units on mechanically and

              biologically treated wastewater

-------
                                                                                      245
The pH values given in the tables are average values of daily samples measured in the laboratory.
They are approximately 0.5 pH units higher than the value measured in the flocculation chamber.
The influence of pH will be studied further on the fifth unit (using flotation for sludge removal)
where a full pH control will be carried out.

The values in Tables 1  to 4 are average for several  24 hr-samples. The samples are mostly from a
period  of about 14 days. The number of samples from which the average values were calculated
varied from 3 to 10. The series with the lowest numbers were supposed to be redone. The points
plotted  in the diagrams are from the tables.

Phosphorus Removal

From January until May  1969 the phosphorus content  of  the raw waste averaged 5.35 mg/l P.
Mechanically treated water from the community plant had in the same period an average of 4.44
mg/l P and the biologically treated water had 3.86 mg/l P.

The curves in Figure 3 show an increase in phosphorus removal with an increasing dose of 75 to
125 mg/l alum for both mechanically as well as biologically treated waste water. From 125 to 150
mg/l there is only a slight increase in the quality of the effluent regarding phosphorus removal.

At the dose of 75 and 100 mg/l with alum there is a significant difference in quality of the effluent
between biologically and mechanically pretreated waste used. Thus, effluent with about 1 mg/l P
can be achieved when treating biologically pretreated wastewater and 3 - 3.5  mg/l P when treating
 Water*
 quality

   R
   B
  B/C

   R
   B
  B/C

   R
   B
  B/C

   R
   B
  B/C
                                         TABLE 3

                               Biological/Chemical Treatment

                              Sludge Removal by Sedimentation

                                   Chemical Dosed: Alum

Chemical dose
alum mg/l
_
.
75
.
-
100
.
.
125
.
-
150
No. of day
samples
for ave. value
4
4
4
7
5
4
4
4
4
8
6
6
  COD
(K2CT207)
  mgO/1

  186.4
  59.1
  49.3

  154.2
  49.3
  38.8

  186.4
  59.1
  33.3

  158.6
  50.6
  34.1
 BOD-T
mgO/1

 94.5
 12.0
 11.5

 97.0
 11.6
  8.5

 94.5
 12.0
  3.5

 98.0
 10.0
  4.7
                                                               Parameters
 Tot. P
mgP/1

 4.65
 4.00
 1.08

 4.45
 3.68
 0.70

 4.65
 4.00
 0.07

 4.45
 3.77
 0.09
Kjeldahl N
 mgN/1

  19.2
  17.1
  15.9

  17.3
  14.5
  14.0

  19.2
  17.1
  15.1

  17.3
  14.9
  14.1
Turb.
JTU

61.0
 4.3
 2.7

47.5
 1.7
 1.4

61.0
 4.3
 0.5

51.8
 2.0
 0.3
 PH

7.30
7.31
6.98

7.59
7.31
6.76

7.30
7.31
6.93

7.56
7.29
6.58

-------
 246

mechanically pretreated wastewater using a chemical dose of 75 mg/l alum. At a dose of 100 mg/l
alum about 0.5 mg/l 0 and 1-1.5 mg/l P can be obtained using chemical treatment respectively.

At the dose of 125 mg/l alum the results vary from 0.07 to 0.32 mg/l P, and at the dose of 150
mg/l from 0.09 to 0.19 mg/l P. Again the best results using chemical treatment were achieved with
biologically pretreated  wastewater.  At these doses  the  difference  between the quality of the
wastewater, pretreated mechanically or biologically, is not significant.

Using acid to lower the pH caused a marked difference in the quality of the effluent from 70 to 90
mg/l alum. From 90 to 100 mg/l  alum there was only a slight increase in the quality.

It seems as if the same  results can be obtained using a dose of 90-100 mg/l alum and pH control
compared to a dose of 125 mg/l alum without pH control regarding phosphorus removal.

Orthophosphate removal followed the trend of total phosphorus removal very closely.


Removal of Organic Matter

BOD7  and COD of the influent and effluent from the chemical treatment plants, as well as the raw
water entering the community plant, were measured. The curves and tables show that BOD and
COD removals follow each other very closely.
                                        TABLE  4
                              Mechanical/Chemical Treatment

                               Sludge Removal by Flotation
                             Chemicals Dosed: Alum and Acid
        Chemical dose
Parameters

Water *
quality
R
M
M/C
R
M
M/C
R
M
M/C
R
M
M/C

Alum
mg/l
.
-
70
.
-
80
.
-
90
.
-
100

H2S04
mg/l
-
-
78
.
-
54
.
-
42
.
-
30
No. of day
samples
for ave . value
8
8
8
5
5
5
4
4
4
3
3
3
COD
(K2Cr207)
mgO/1
172.1
199.0
61.0
201.1
193.3
60.0
155.0
156.2
39.4
178.6
132.5
31.6

BODj
mgO/1
98.4
132.3
17.6
87.0
104.5
18.0
91.8
125.5
15.5
102.0
90.5
7.3

Tot.P
mgP/1
4.37
5.61
2.41
5.04
5.76
1.74
4.75
4.68
0.56
4.90
5.00
0.25

Kjeldahl N
mgN/1
18.5
22.9
17.9
22.6
28.0
21.1
20.8
19.8
16.7
21.8
22.5
16.2

Turb.
JTU
30.1
45.9
5.3
48.4
109.0
6.7
54.0
40.1
2.5
31.7
22.2
0.7

PH
7.66
8.03
5.11
7.57
7.58
6.48
7.29
7.28
6.72
7.24
7.32
6.72
R = Raw wastewater
M = Mechanically treated
B = Biologically treated
C = Chemically treated

-------
                                                                                                        247



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Mec



l_



                               70      80      90
                                    Alum dose mg/l
                                                                  ige           1 76.9 mg 0/1
                                                          Mechanically treated   178.0 mg 0/1

                                                          Mean values:
                                                          Raw sewage           94.1mgO/l
                                                          Mechanically treated   118.4 mg O/l
                                70      BO      90      100
                                      Alum dose mg/l

Q.
P 3


4
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R«
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-
                                                                  age          4.47 mg P/l
                                                           Mechanically treated   5.37 mg P/l
                                70      80      90      100
                                      Alum dose mg/l
                         O        Mechanical-chemical  treatment on flotation unit with dose of acid
                         	Mechanical-chemical treatment on flotation unit without do» of acid

FIGURE  4   Results  by   dose  of  alum  and  acid  at  flotation  unit  on   mechanically  treated
               wastewater

-------
 248


 The   difference  in   the  removal  is  larger  between  mechanical/chemical  treatment  and
 biological/chemical treatment for organic matter compared to phosphorus removal. This  is also
 true when a high alum dose is used.

 A dose of 75 mg/l alum gives only a slightly lower BOD and COD with chemical treatment. An
 increase in dose up to 125 mg/l alum gives better removal, especially on mechanically pretreated
 waste. An increase in chemical dose from 125 to 150 mg/l alum gives only a small improvement in
 organic matter.

 It is most important that mechanical/chemical treatment using a dose of  125 to 150 mg/l alum
 gives  an  effluent regarding organic matter which has the same quality  as biologically treated
 wastewater.  From the  curves and tables it  is shown  that biological treatment gives a COD
 reduction from 203 to  53 mg/l, and BOD7 reduction from 112 to 10 mg/l. With a dose of 125
 mg/l alum using mechanically treated water, an effluent of 45 mg COD  and  11 mg/l BOD was
 achieved.

 The results from a combined dose of 100 mg/l alum and pH adjustments are somewhat better than
 using  125 mg/l alum without pH adjustments. The curve is steeper in the range of 90 - 100 mg/l
 alum with acid than it is in the range of 125 -150 mg/l alum without acid.  It seems therefore that
 a higher dose of alum could give better results regarding organic matter when pH adjustments are
 made.

 Other Components

 Removal  of turbidity followed phosphorus removal very closely. Aluminum residual was measured
 in the effluent  and was thought to be a good parameter to control the process, but experience
 showed that turbidity and  pH gave better information on the conditions of the plant, and were
 easier  to  observe. Turbidity and  pH seemed  to be the parameters most  likely  to  indicate the
 efficiency of the process.

 Nitrogen  has been analyzed as  Kjeldahl-nitrogen and  as a sum  of  nitrite-nitrate  nitrogens.
 Reduction of  Kjeldahl-nitrogen  was moderate by  chemical  treatment when using alum as  a
 coagulant both  with or  without control of pH. There were only slightly better results when the
 chemical dose was increased. The amount of nitrogen was reduced from 20 - 15 mg/l N in the most
 effective experiments.

 Nitrite-nitrate has always been below 1 mg/l N in the raw mechanically and biologically treated
 water. By the  chemical treatment there  has  always been a tendency  for  higher  values of
 nitrite-nitrate in the effluent compared to the influent for mechanically and biologically pretreated
 wastewater. However,  the values have always been lower than 1  mg/l N except in two  cases.
 Nitrite-nitrate always makes up less than 5% of the total nitrogen.

Average value of hardness for the wastewater treated was 1.7 dH. The experiments using alum and
acid  show higher values of most parameters for mechanically treated water as for the raw water.
The  reason for this has not yet been found. It may have  a connection with the accumulation of
suspended solids in the return surplus sludge from the biological units to the mechanical units.

-------
                                                                                     249
                  TREATMENT COST AND  PRACTICAL EXPERIENCE
The type of alum used so far is delivered at a price of 350.-N.kr/ton in Oslo. The price for sulfuric
acid is 225.-N.kr/ton in 95% concentration. The prices are:

                            125 mg/l alum         4.37 0re/m3
                        100 mg/l alum + 30 mg/l H2SO4  4.21 0re/m3
                               (1 N.kr = 100N.0re  = $0.14)

The difference  in  price  when using one  or  two chemicals is small. The prices will differ for
different places in Norway,  and other countries may have different prices. Treatment efficiency
and economical aspects should be evaluated in each case.

Sludge production was measured, but is not presented in this paper. It is obvious, however, that
sludge  production decreases with decreasing doses of alum. This may  be  a  deciding factor for
choosing two chemicals rather than one.

It will probably be unusual to use two chemicals at smaller treatment plants. (In Norway there will
be a large number of treatment plants serving less than 5,000 persons). The lower cost and smaller
sludge production by using two chemicals will not outweigh the extra operational difficulties.

At larger treatment plants, however,  reduction in operational costs is more important. It  is more
economical to invest more in equipment and automatic control of chemical dosing to reduce the
cost of operation.  Reduction in sludge production will also be more important at large plants. At
such plants one will get full  advantage through the combined dose of alum and acid, if prices are
such that this combination gives the lowest running cost.

Flotation is not suggested for small scale treatment for economical and  operational reasons. This
process has more  mechanical equipment and requires highly skilled personnel. Effluent to  be used
as dispersion water should have good quality to avoid clogging.

For larger plants  these  reservations  should  be  easily  overcome. Using flotation decreases the
construction cost even though the process needs more mechanical equipment.

The type of  alum used for  the  experiments contains some very  fine insoluble impurities. These
have a tendency to settle in  pipes before they are mixed with the wastewater, thus clogging valves
and pumps. They may also cause wear on  pumps. The company  Boliden, which is delivering this
alum, has made suitable equipment for dosing the chemical.

It |s  assumed  that  chemical treatment is  less affected by low  temperatures  than biological
treatment. Therefore the effect of temperature was not considered during these experiments. The
testing was  run  under  the climatic  conditions  in  Oslo  which  are not extreme. Outdoor
temperatures may  be 20 - 25° C below zero for about one month. The wastewater temperature is
decreased to about 5° C.

Construction costs for  biological and chemical treatment is evaluated by Dr. Wuhrmann (1967) to
be about 30% higher than conventional biological treatment by the activated sludge method. The
costs for mechanical/chemical treatment plants were estimated to  be about 20% less than the costs

-------
 250


 for conventional biological treatment plants. Such a consideration will be valid for treatment
 plants larger than about 5,000 persons. Costs of smaller chemical treatment plants can be higher
 than biological treatment plants.

 With  the results  from the experiments regarding removal of phosphorus  and organic matter, it
 seems that mechanical/chemical treatment should be considered first where eutrophication is the
 greatest  problem in the receiving waters and phosphorus is the most important nutrient to be
 removed from the wastewater.

                               FUTURE INVESTIGATIONS

 We had an extensive program  for future investigations using the five plants. It was interrupted by
 the fire in May, when the four sedimentation plants were totally damaged. There is a great need
 for further investigations, and the work will be continued.

 The experiments using the flotation plant will be continued with Norwegian alum. pH equipment
 will be enlarged to  cover automatic dosing of chemicals through pH control. Studies will then be
 continued to find the most suitable and economic operational conditions using alum and acid.

 Further, it is of great interest  to find practical methods for using ferro-sulfate as a coagulant. This
 is an  industrial  waste product  and will  probably be  the cheapest coagulant  in Norway.  From
 laboratory studies (Henriksen, 1962 and 1963} it seems that it should be an easy and inexpensive
 way to oxidize the iron from di-valent to tri-valent before or during the coagulation process.

 We are also interested in studying coagulation using lime and stripping of ammonia by aeration at
 high pH.

 All investigations will be preferably carried out simultaneously  on mechanically and biologically
 treated  wastewater.  We are  also  interested  in studying  direct chemical treatment  on  raw
 wastewater.


                                     REFERENCES

 Camp, S. (1943)  Velocity Gradients and Internal Work in Fluid  Motion, Boston Soc. Civ. Eng., p.
     219.

 Henriksen, A. (1962) Laboratory studies on the  removal of  phosphates  from sewage by the
    coagulation process, Schweizerische Zeitschrift fur Hydrologie, Vol. 24, p. 253.

 Henriksen, A. (1963) Laboratory studies on the  removal of  phosphates from sewage by the
    coagulation process, Part 2, Schweizerische Zeitschrif t fur Hydrologie, Vol. 25, p. 380.

 Popel, J.  (1966) Die Elimination von Phosphaten, Kommisionsverlag R. Oldenburg, Munchen.

Stumm, W. and Morgan, J. (1962) Chemical aspects of coagulation, J. Amer. Wat. Works Assoc.,
    Vol. 54, p. 971.

Stumm, W. (1962) Discussion  to paper by Rolich, G. A.: Methods for the removal of phosphorus

-------
                                                                                  251
    and  nitrogen  from sewage  plant  effluents. Advances  in Water  pollution  research,  Proc.
    Internal. Conf. London, Vol. 2, p. 216.

Thomas, E. A. (1962) Verfahren zur Entfernung vor Phosphaten aus Abwassern,Schweiz, Patent
    361543.

Wuhrmann,  K.  (1964)  Stickstoff-und  Phosphorelimination, Ergebnisse  von  Versuchen  im
    Technischen Masstab, Schweizerische Zeitschrift fur Hydrologie, Vol. 26, p. 520.

Wuhrmann,  K.  (1967)  Probleme der  dritten  Reinigungsstufe von  Abwassern,  Federation
    Europaischer Gewsser schutz (PEG) Informationsblatt Nr. 14.

-------
    BIOLOGICAL  AND CHEMICAL WASTE  TREATMENT EXPERIMENTS
                          IN  FAR  NORTHERN SWEDEN
                                      Peter Balmer
                                    INTRODUCTION

     ,,wn of Kiruna is situated at 68° north latitude (Fig. 1) and is hence the northernmost town
in Sweeten In the winter, temperature extremes of  35  C ( 3CT F) occur

The existing primary treatment plant was overloaded  and the town  planned to replace it with a
new plant with primary and activated sludge treatment
The know how of design of an activated sludge plant for tre<
limited  at this  time (1962   1963)  In a literature  rev.ev
Ijijoutory data clearly showed that the metabolizing ai
      i.-
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                                                                                     253


                    EXPERIMENTS  WITH BIOLOGICAL TREATMENT

Activated Sludge Experiments

Apparatus

The pilot plant consisted of three aeration tanks mounted in series wtih working volumes of 2.0
m3 (71 cu ft), 2.0 m3  (71 cu ft), and 1.7 m3  (61 cu ft). The settling tank was conical with a
volume of 2.7 m3 (96 cu ft) and a surface area of 2.5 m2 (270 sq ft). The  tanks were provided
with inserted walls so that back-mixing was minimized. Air was supplied through perforated plastic
piping  on the  bottoms  of the tanks.  Sampling (24-hour composites) was done with automatic
samplers.

Sewage

The experimental unit was supplied with presettled sewage from the existing plant in Kiruna. The
Kiruna sewage  is almost entirely of domestic origin. The strength of the sewage is, however, quite
low.

Experiments

During June,  1963 to May, 1964, 6  runs were made. The details are extensively described in
duplicated reports (Balmer, Berglund and Granstrand, 1964; Balmer, Berglund and Widell, 1964)
(in Swedish) and summarized by Gustavsson and Westberg (1965).

The operating  conditions during the runs are given  in Table 1, and detention  times and calculated
load factors are  shown  in Table 2. In all  runs except run 3 the unit was run as  a conventional
activated sludge process. In run 3 the  unit was run according to the contact stabilization principle
with step addition of return sludge (Balmer, Berglund and Enebo, 1967). Flow-sheets for the runs
are given in Figure 2.

                                        TABLE 1

                                 Mean Operating Conditions
Period
1
2
3*
,4
5
6
Length
of run
days
33
34
17
19
11
24
Temp.
9.4
7.8
6.3
5.8
3.7
5.4
Sewage
flow Recirculation Air flow
m3/hr ratio m /hr
1.47
1.36
1.21
0.96
1.19
1.80
0.42
0.42
0.45
0.42
0.34
0.33
14
28
31
24
26
21
Suspended solids
in aerator
ppm
3,000
3,600
3,300/4,200
3,600
3,200
2,300
Oxygen concentration
tank 1 tank 2 tank 3
ppm ppm ppm
0.4
0.7
0.0
0.9
4.4
2.3
0.8
1.0
0.0
1.1
4.0
2.3
1.0
1.4
0.4
2.7
6.9
2.3
*Step addition of return sludge. Suspended solids concentration in return sludge aeration tank
12,400 ppm.

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254
                                     PERIOD 1-2, 4-6
                                     PERIOD 3
   AERATION TANK
   EFFLUENT
t  * INFLUENT
R * RETURN SLUDGE
S - SETTLING TO*
SA* SLUDGE AERATION TANK
                FIGURE 2  Flow sheet of experimental runs (June 1963-May 1964)
 Results
 Mean  results from the 6 runs are presented in Table 3. In period 1 steady state conditions were
 probably not reached.

 The oxygen content in the aeration tanks was very low throughout periods 1  - 3, indicating that
 oxygenation capacity of the equipment  was the  limiting factor. In periods 4  - 6  the  oxygen
 content in the tanks was higher although the oxygen supply was lower compared to periods 2 and
 3. It is therefore probable that bacterial activity was the rate determining factor in these periods.
 The mean temperature difference between periods 3 and 4 is small and the difference in bacterial
 activity is probably not as  large as the differences in oxygen  concentration in the aeration tanks
 may indicate.  The low oxygen concentration during period 3 (contact stabilization) is  explained
 by the large amount of suspended  solids in the reaeration tank (tank 1} and the  rather high  load on
 the two aeration tanks.

 The conclusions of the activated sludge experiments in pilot plant scale were:

     Biological treatment is possible at temperatures as low as 3° - 4° C (37° - 39° F). The  activity
     of the activated sludge is seriously affected by low temperatures. Long aeration periods are
     necessary. If a low BOD sewage is treated, a period of at least 4 hours is required to reach an
     effluent BOD of 20 - 25 ppm.

     The contact  stabilization technique is attractive as it gives a larger amount of sludge  actively
     metabolizing in a given aeration volume.
As biological treatment now was proved feasible, the town planned to build a treatment plant

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                                                                                      255
          Detention time
             aeration
Period          hr
  1             3.9
  2             4.2
  3             3.1*
  4             5.9
  5             4.8
  6             3.2
TABLE 2
Load
Detention time
settling
hr
1.8
2.0
2.2
2.8
2.3
1.5
Factors
Surface load
settling
m /m* , hr
0.59
0.54
0.48
0.38
0.48
0.72
         BOD-load
       kgBOD/m3,d
           0.34
           0.46
           0.41
           0.40
           0.40
           0.41
Sludge load
kg BOD/kg
 sludge, d
   0.11
   0.13
   0.06
   0.11
   0.13
   0.25
*Detention time in aeration tanks only. Detention time in return sludge aeration tank was 3.7 hr.
consisting of presettling and secondary treatment with activated sludge. The primary treatment
unit was first erected and was put into operations in 1967.

                     EXPERIMENTS WITH  CHEMICAL TREATMENT
In the years since the activated sludge experiments,  there has been a complete turnover in the
opinion on  the  value  of  biological  treatment.  Biological treatment is now considered of very
limited  value as the  initial BOO  load caused by domestic effluents  in the receiving waters is
considered low in  relation to the  secondary pollution caused by nutrients, mainly phosphorous
compounds.
It was then  discussed whether the  planned addition of aeration tanks and secondary settling tanks
could be replaced advantageously with a coarse presettling basin and a f locculation basin placed in
front of the  existing settling tanks, as illustrated in Figure 3.

                                        TABLE  3
                       Analytical Results - Activated Sludge Treatment
                    INFLUENT
EFFLUENT
Period
1
2
3
4
5
6
BOD 5
ppm
55
81
80
83
82
76
Suspended
solids
ppm
46
84
56
54
54
51
Setteable
solids
ml/1
1.7
1.0
0.7
1.0
1.1
0.4
BODS
ppm
13
15
10
20
20
24
Suspended
solids
ppm
29
14
16
18
21
7
Setteable
solids
ml/1
0.5
0.1
0.1
0.1
0.1
0.1
No. of
composite
samples
10
12
4
9
6
9

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 256
                                     ACTTVATEO SLUDGE TREATMENT
                                           CHEUCAL TREATMENT
                                                          A-AERATION BASIN
                                                          F'FLOCCULATKM BASIN
                                                          S* SETTLING BASIN
                                                          DOUBLE UNE • EXISTING UNIT
                   FIGURE 3  Two ways to enlarge a primary treatment plant


 As a preliminary economic analysis also indicated that chemical treatment could be cheaper, this
 seemed to be an attractive alternative. In order to determine the treatment efficiency of a chemical
 treatment process, the town had to carry out pilot plant experiments.

 Experiments with Flocculation and Settling

 Apparatus

 The pilot plant  equipment (Fig. 4) consisted of a flocculation tank and a settling tank. The
 flocculation tank was divided  into 4 compartments, each with a working volume of 0.23 m3 (8 cu
 ft). The compartments were provided with paddle-type mixers with peripheral speeds of 0.5. 0.35,
 0.25, 0.15 m/s  (1.6. 1.2. 0.8, 0.5 ft/s)  respectively. The  settling tank  was  rectangular with  a
 volume of 2.0 m3 (70 cu ft) and a surface of 2.0 m2 (220 sq ft).

 The flocculated sewage was transferred from the flocculation tank to the settling tank through a
 siphon with a diameter of  10  cm (4 in). Sampling (24-hour composites) was done with automatic
 samplers.

 The equipment proved suitable for  its purpose although the peripheral speeds of the mixers in the
 2 last compartments was somewhat too fast. The transfer from the flocculation tank to the settling
 tank also destroyed some floes.

Sewage
The pilot plant equipment was fed with domestic sewage that was pumped from the inlet zone of
one of the primary settling basins in the new treatment plant. In this way a coarse presettling was

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                                                                                       257
                         FIGURE 4  Pilot plant for chemical treatment


 simulated. The sewage was almost entirely of domestic origin and the temperature  of the sewage
 was about 3° C (37° F).

 Experiments

 In 4 experiments different amounts of technical grade alum (8.1% Al) were added to the sewage.
 In one of the runs, addition of an anionic polymer (Dow Purifloc A-23) was tried.

 The flow through the apparatus was 0.96 m3/hr (4.2 gpm) which means a detention time in the
 flocculation tank of about 1 hr, and of 2 hr in the settling tank.

 Results

 Mean results from the test runs are given in Table 4.

 Experiments with Simplified Chemical Treatment

 The Treatment Plant

 The sewage  treatment plant in Kiruna consists of a  coarse bar screen, an aerated grit chamber, a
 comminutor and three parallel settling basins. Each  settling basin has a width of 6 m (20 ft) and a


 length of 47 m (148 ft) and has a total volume of 640 m3 (22,800 cu ft). During the test week the
flow through the plant was almost the same every day. Flow and load factors of the settling basins
are given in Figure 5.

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   258
                                      TABLE 4

                         Analytical Results - Chemical Treatment
                        INFLUENT             EFFLUENT
FILTERED EFFLUENT
Alum                                                                              No. of
dosage Flocculation BOD7 COD Phosphorus BOD7  COD Phosphorus BOD7 Phosphorus Composite
ppm
100
120
120*
150
PH
6.6-6.9
6.4-6.9
6.4-6.9
5.2-5.5
ppm
60
50
52
81
ppm
24
25
30
33
ppm
6.5
2.9
4.3
3.9
ppm
41
27
26
33
ppm
18
15
19
19
ppm
2.3
0.62
0.64
0.79
ppm
28
24
20
25
ppm
0.20
0.39
0.35
0.10
samples
4
3
3
3
*1 ppm Dow Purifloc A-23 added. COD was determined with potassium-permanganate oxidation.
   FLOW
   900
   800
   TOO
  600
   500
  400
  300
  200
   CO
                                      —  FLOW
                                      —  SURFACE LOAD
                                      —  DETENTION TIME
                                    (2
       DETENTION TIME, h
       SURFACE LOAD m /m, h
                                                                  2
          FIGURE 5   Wastewater flow and detention time and surface load on settling basins

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                                                                                     259
                                        TABLE 5

                    Operating Conditions - Simplified Chemical Treatment

Date                     Time                  Alum dosage               Flocculation-pH
                                                   ppm

12/1                  1100-2200                    141                       6.0-6.4
13/1                  1300-2200                    142                       5.8-6.1
14/1                  0900-1700                    122                       6.6-6.8
15/1                  0800-1600                    117                       6.0-6.4
15-16/1               2200-1300                    90                        5.7-6.2
17/1                  0500-1000                    100                       6.0-6.3
17/1                  1000-1600                    140                       6.4-6.5
Experiments

Technical grade alum  was added as a 20% solution to the influent sewage just ahead the grit
chamber. The flow of alum was adjusted over the day so that a constant dose of alum per unit
volume of sewage was achieved. The operating conditions are presented in Table 5.

Results

Results of the full-scale experiments are presented in Table 6 and  Figure 6.

If the effluent quality with the biological treatment (Table 3) is compared to the insults achieved
with the  chemical  treatment  (Table  4,  Table  6 and  Figure 6), it  appears that the chemical
treatment gives almost as low BOD values as the biological treatment. Furthermore, the chemical
treatment removes up to 90% of the phosphorus content of the sewage.

The results of the full-scale experiment indicate that separate flocculation basins may be omitted.

Visual  observations during the experiments revealed that the flocculation pH should be controlled,
as pH over 6.7 yielded a floe with poor settling properties.

Sludge Handling

In Kiruna the normal amount  of primary sludge  is 50-70 g total solids per capita per day. When
alum is added to the sewage, this amount increases to about 100 g total solids per capita per day.
During the full-scale experiment the total solids concentration of the sludge  fell from the normal
5-8% down to 2-3%. The sludge volume hence increased to about 4 times the normal.

The sludge dewatering equipment  in Kiruna consists of a "roto-plug" gravity dewatering drum
followed by  a screw press. The equipment captures 80-90% of the total solids in the primary
sludge. With  chemical  treatment  sludges the solids capture was down to  about 30%. Cationic

-------
260
PHOSPHOROUS
ppm
6-


5 -

4 •


3
2
1
ppm
BO-
100-


50


vn
minrnn OPERATION TIME
K^sSH INFLUENT
1 1 EFFLUENT










n







a
\
\
%
I
y
%
!

Y
^
y.
X
X





1
y,
y
X
/^
^
y
X
X
1















1
A
X
^




1
I2J 	 HJ 	 14)
0 12 0 12 0 12











7}
y
y
Y,
^
i
y.
y









^
f**
1
faw
yW/
v$

771




\ 	
V
X
X
^
|




n
\ ^
u

0 12 0










n \












"
/
/
/
/
/ /
^
/
/
/
/
/
/
(1




?
',
1 1 rrl
r T
12 0
y






12 0
FIGURE 6 Operation time with chemical treatment and phosphorus and BOD7 in influent and
             effluent
 polymers had a very good conditioning effect on the sludge, but the dynamic action of the sludge
 dewatering equipment destroyed the floes formed by the polymers. It is, however, believed that
 the sludge could be successfully dewatered with static-type dewatering equipment.

                                CONCLUDING  DISCUSSION

 The experiences with the activated  sludge treatment have proved that biological treatment  is
 possible even at very low sewage temperatures. As the metabolizing activity of the activated sludge
 bacteria is considerably  reduced, long aeration periods, 4-5 hours, and  therefore large aeration
 basins, are required.

 A chemical treatment is  much less sensitive to low temperatures and requires only about 0.5 hour
 detention time in the flocculation tanks. The difference in investment costs will in many  instances
 be so large that the increased running costs are justified.  '

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                                                                                    261
If a community has an existing primary treatment plant with a long detention time (more than 2
hours), it may be possible to achieve a substantial increase in treatment efficiency just by a simple
addition of flocculating chemicals to the influent.

The BOD removal with chemical treatment is somewhat inferior to  what can be achieved with
biological  treatment. This  drawback,  however, is compensated by the  superior phosphorus
removal.
                                        TABLE  6
                     Analytical Results - Simplified Chemical Treatment
                   INFLUENT
EFFLUENT

Date
12/1
13/1
14/1
15/1

16/1




17/1




Time
1930-2130
1840-2140
1220-1530
1000-1400

0000-0300
0300-0600

0600-1100

0530-0730
0730-0930
0930-1130
1130-1330
Suspended
solids
ppm
120
110
130
110

60
15

52

4
7
59
98
COD
ppm
33
35
35
40

19
7

19

6
7
30
42

Time
2100-2245
2030-2230
1500-1820
1300-1500
1500-1715
0320-0520
0520-0720
0720-0920
0920-1120
1120-1400

1030-1230
1230-1430
1430-1530
Suspended
solids
ppm
24
14
40
13
17
26
20
17
33
20

8
16
16
COD
ppm
14
13
16
11
11
15
9
18
9
17

8
15
18
Aluminum
ppm
1.3
1.3

1.6
1.1
0.8
1.4
1.3
0.8
1.0

0.8
1.1
1.3
 *COD was determined with potassium-permanganate oxidation

-------
262
                                     REFERENCES
Balmer, P., Berglund, D. T. and Granstrand, G. 0964) Report to the town of Kiruna about
     activated sludge experiments, I. (in Swedish).

Balmer, P., Berglund, D. T. and Widell, A. (1964) Report to the town of Kiruna about activated
     sludge experiments. III. (in Swedish).

Balme'r, P., Berglund, D. T. and Enebo, L.  (1967) Step-sludge - a new approach to wastewater
     treatment, J. Water Pollut. Cont. Fed., 39:1021.

Gustavsson, B. and Westberg, N.  (1965) Experiments with treatment of sewage from the  town of
     Kiruna with the  activated sludge method,  (in Swedish),  Royal Institute  of  Technology
     Publications. Vol. 4.

Hilme'r, A., The  influence of temperature on the activated sludge process, (in Swedish), Royal
     Institute of Technology Publications.

-------
      BIOLOGICAL  SEWAGE TREATMENT  IN  A  COLD  CLIMATE  AREA


                   Shigeo Terashima, Keichi Koyama, and Yasumoto Magara


                                     INTRODUCTION

 Recently many sewage treatment plants using activated sludge processes have been installed in the
 Hokkaido  and Tohoku districts  which are  cold  climate  areas in  Japan.  In these plants  it  is
 necessary to give attention to low sewage temperature in winter and thaw seasons.

 The rate of  run-off is  often  about  twice dry weather flow.  Thawing flow carries the turbid
 substances  that  were piled up in winter and lowers the sewage temperature. Therefore,  it  is
 considered  that thawing flow affects  sewage treatment process, but no reports about the effect of
 thawing are available.

 The removal  characteristics of BOD and nitrogen  at the Souseigawa municipal sewage treatment
 plant (Sapporo, Japan) from March 1967 to February 1970, are shown in Table 1.

                                        TABLE 1

               The Effect of Temperature on Purification at the Souseigawa Plant

 Sewage temp.                 BOD removal (%)                 (Org-N. + NH3-N.) removal (%)

   <10°0C                          82                                    0
   11-1/C                         82                                   23
   >16 C                          87                                   25

 This shows  that nitrogen removal ceases below 10° C but BOD removal is little affected by sewage
 temperature. It is assumed that there  is a different effect on BOD and nitrogen removal activity of
 activated sludge.

 The activated  sludge process is composed of (1) removal of wastes, mainly by biosorption, after
 contact of the waste with activated sludge, (2) removal of wastes by the anabolism and catabolism
 of  the absorbed  substrate, (3)  aeration  to  supply  the  oxygen  for these reactions and,  (4)
 solid-liquid  separation.  Several reports  have  been published  on  the effect of  temperature on
 activated sludge processes (Banerji, 1965).  Ludzack et al. (1952) showed that sewage temperature
 had little effect on the activated sludge. The waste removal at 30° C was 10% higher than at 5° C,
 but the solids yield was  greater at 5°  C than 30° C. (Keefer, 1962) reported operating results over
 a 20-year period for a municipal sewage treatment plant. The variation of the average percent BOD
 removal with temperature  was dependent on  the flow and  increased as  the organic load was
 increased. Okun  (1949)  reported little effect of temperature on BOD removal in the activated
 sludge process between 8-35° C.

These reports discussed the overall effects of temperature on the activated sludge process and were
not investigations  of each individual process component of the total system. There have been no
investigations on compounds other than BOD.


                                          263

-------
 264


 It is necessary to investigate the effect  of each process and  to know what process is  mainly
 affected  by sewage temperature. It  is possible to have a good activated sludge plant in a cold
 climate area by strengthening that process mainly affected by sewage temperature.

 We have  been  investigating the thawing effect on sewage and the effect of low sewage temperature
 on the activated sludge process. This paper deals with the effects of thawing and the effects of low
 sewage  temperature on the aeration process,  substrate  removal,  nitrification and  settling
 characteristics  of activated sludge.

                       THE EFFECTS OF THAWING ON  SEWAGE

 Procedures

 Thawing is affected by  atmospheric temperature, sunshine, rainfall, underground temperature, etc.
 Atmospheric temperature is considered the primary influence for run-off analyses. Degree-days
 and degree-hours are used as indices of atmospheric temperature. The degree-day is defined as the
 cumulative number of  daily mean atmospheric temperatures above 0° C within a  certain period,
 and degree-hour as the  cumulative number of hourly atmospheric temperatures above 0° C within
 the  day. Sewage  drainage  areas are more affected by  atmospheric temperature than  river
 catchment areas because sewage drainage areas are very limited and thawing is directly related to
 hourly change of atmospheric temperature. So, the degree-hour  is used  as an index of thawing
 run-off analysis.

 We investigated two sewage drainage districts at Sapporo, Japan. Their characteristics are shown in
 Table 2.

                                        TABLE  2

                            Characteristics of Drainage Districts

                                    Souseigawa District                  Makomanai District

 Drainage Area                       623 ha (April 1968)                 37 ha (April 1968)
                                    736 ha (April 1969)
 Population                          125,090 (Dec. 1967)
 Sewer System                        Combined system                   Separate system
 Type of District                     Urban area                         Residential area

 The rate and quality of sewage flow were observed  at the receiving well of the sewage treatment
 piant (1968) or at the final pumping station  (1969)  at the Souseigawa district;  the same were
 examined at the outlet of  the storm  sewer at the Makomanai district. Sewage was analyzed for
 temperature, pH, 4.3 alkalinity, chloride  ion (CO, total residue (T-Re), suspended solids  (SS),
 chemical oxygen demand (COD),  biological oxygen demand (BOD), organic nitrogen (Org N),
 ammonium  nitrogen (NH3-N), nitrite nitrogen (N02-N), and nitrate nitrogen (NO3-N) according
 to the 12th edition of Standard Methods (1965). Sampling was done at 3:30  PM - 4:00 PM
 (Souseigawa district) and 2:30 PM - 3:00 PM (Makomanai district). In Sapporo, it was  most
 probably  to find  the  highest atmospheric ternperature at about  2:00 PM. Therefore  it was
considered that this sample was  most affected by.thaw. To  calculate  the degree-hour, an
atmospheric temperature was summed from 3:00 AM to the  next day at 3:00 AM. The  rate of
thawing  run-off was gained by reducing the dry weather flow (55,000 M3/d-1968. 60,000

-------
                                                                                      265
M3/d-l969) from the total rate of sewage flow. If there was a rainfall, the rate of storm run-off
was reduced.

Results and Discussion

The Rate of Thawing Run-off

Figures 1,  2 and 3 show the daily aspects of a degree-hour and the rate of thawing run-off. The
relationships between a degree-hour and the rate of thawing run-off are shown in Figure 4. The
next empirical formulas (1-1), (1-2), and (1-3) are attained from this relationship.
Souseigawa district
     March 1 -April 6, 1968

     correlation coefficient r = 0.87
Qt =  0.743AD + 17.2A
     March 6 - March 26, 1969 (excluding March 21)
                                  Qt =  0.747 A D + 27.7A
     correlation coefficient r = 0.94

 Makomanai district
     1969 (duration of cold days)
                                   Qt  = 0.14AD + 9.7A
     correlation coefficient r = 0.94
 Here, Qt  = the rate of thawing run-off (M3/D)
     D =  the degree-hour (° C hr.)
     A =  drainage area (ha)
      I
                ORATE OF THAWING RUN-OFF
                • DEGREE  HOUR
      \
      |
      fe
      I
(1-1)
                                                    (1-2)
                                                    (1-3)
                                          DATE
         FIGURE 1   Rate of thawing runoff and degree-hour (Souseigawa district, 1968)

-------
266
                         O RATE OF THAWING RUN-OFF}
                         • DEGREE HOUR
                                       IS      20
                                          DATE
         FIGURE 2   Rate of thawing runoff and degree-hour (Souseigawa district, 1968)
               Ik
               ?
                  I750
                  1500
                  1250
                  1000
               o  750

               in
               tc
                  500
                  250
—O—   RATE OF THAWING RUN-OFF   (mVDAY)
--Q	P.M. 3-30,  RATE OF THAWING RUN-OFF (-j^ mtonW
—•	  DEGREE HOUR
        FIGURE 3   Rate of thawing runoff and degree-hour (Makomanai district, 1969)

-------
                                                                                     267
         •S
           CO
           5
         P
         x!2
         "W
         fc3
         "in
         a:
100
               75
               50
—O	 SOUSEIGAWA DISTRICT (1968)


—CD	SOUSEIGAWA DISTRICT (1968)
                                                        CD
                                      O
                                             —-©— MAKOMANAI DISTRICT
                        o
                         25      50      75      100

                                   DEGREE HOUR — "C hr
                                                         125
                                                                 BO
                                                           10.0
                                                           7.5  fcS
                                                      5.0  i |


                                                            I
                                                               5
                                                                          2.5
                                                                              
-------
             200
                                    COEFFICIENT OF CORRELATION

                                         *  0985
                 v       60      CO      60      200

                       OBSERVED  VALUE - "C hr

 FIGURE 5   Correlation between observed and calculated degree-hour
               TO
           #   60
           I
               40
               2
                                      COEFFICIENT OF CORRELATION
                                              • 036
                    COEFFICENT OF CORRELATION
                          -0*7        O
                  345678

                            WATER TEMPERATURE - "C
FIGURE 6  Correlation between water temperature and runoff percentage

-------
                                                                                      269
very significantly affected by thawing inflow. However, at the Makomanai district, there was poor
correlation compared  to the Souseigawa district during the season.  Hourly observation data
(Figure 7) shows  the reason why significant correlation was not attained. The correlation at the
end  of the season differed from  that  at the  beginning. This was caused by changing sewage
temperature, influenced mainly by ground temperatures.

Suspended matter was increased up to 1,500 mg/l at the Makomanai district and up to 500-600
mg/l at the Souseigawa district by thawing. The correlation of suspended solids and percentage of
thawing run-off at the Souseigawa district is shown in Figure 8-1. The correlation of suspended
solids and run-off rate at the Makomanai district is shown  in Figure 8-2. Each figure  shows that
suspended solids and chemical oxygen demand attributed to suspended solids increase accordingly
with increments of  thawing  run-off. The results of the Makomanai district show that thawing
run-off in early periods contains much turbidity compared with final periods.
                                                                       o
                                                                       «

                                                                       UJ
                                                                        ir
                                                                        UJ
                                                                        te.
                                                                        I
                           10
                          FIGURE 7  Hourly observation at Makomanai

-------
 270
               8!
               I
                  100
                  80
               I  eo


               S-
               5
                          —   500

                                        SUSPENDED SOLIOS-i.j/1



                                   O Mv. 26
                              9.9
                                              Mm 17
                                    50    100   200   2SO   300

                                          COO,, my|
                                                          020 V




                                                          O.B  |:




                                                          0.10  o
                                                              u



                                                          OjQS
FIGURE 8-2  Correlation  among rate of runoff and  suspended solids, COD   (Makomanai
              district)                                                      ss

-------
                                                                                       271
Other components of the sewage  are shown in Figure 9. The figures show that generally each
component, except chloride  and nitrate,  increases with temperature decrement which relates to
the rate of thawing run-off. However, the range of those fluctuations was not so large as to affect
the sewage treatment facilities.
                  9

                  8

                  7

                  6
                          246
                          WATER TEMR--C
                     2      4
                      WATER TEMP.-*C
                  20
                  10
                          246
                          WATER TEMP.-»C
          _  1.0
          f
          I
          ^> 0.5
                     £46

                     WATER TEMR-°C
                -0.08

                E
                I
                fo.04
                f  2
o
                           246

                             WATER  TEMR-"C
                          246
                            WATER TEMP.-'C
                                                   20
                                                    10
                                                   40
                                                 3
                      246

                      WATER TEMR-°C
                     2      4      6

                      WATER TEMR — "C
                             FIGURE 9  Various sewage components

-------
 272

 Conclusion

 The rate of thawing run-off significantly relates to the degree-hour. If these correlations are known
 for a certain drainage area, it is possible to predict the rate of thawing run-off from the highest and
 lowest atmospheric temperatures of the day. However, these correlations become  less obvious at
 the end of the thaw season.

 Sewage temperature and suspended solids are significantly affected by thawing run-off, especially
 when sewage temperature drops below 5° C.
                    THE EFFECT OF LOW SEWAGE TEMPERATURE
                        ON THE ACTIVATED SLUDGE  PROCESS

 The Effect of Sewage Temperature On Oxygen Transfer

 Procedures

 The effects of temperature  on oxygen transfer in a diffused aeration tank were investigated by
 measuring the  oxygen transfer coefficient at every 5° C decrement from 25° C to 5° C under a
 fixed rate of air flow.

 Completely mixed aeration tanks were  used, with porous plate diffusers installed in the bottom.
 The aeration  tank  is shown in Figure 10. The oxygen transfer coefficient was obtained by a
 non-steady state procedure {Eckenfelder, O'Connor, 1961) under stabilized operating conditions.
 The aeration tank was filled to a desired volume with tap water. Dissolved oxygen in the water was
 removed  by admitting nitrogen gas. After the dissolved oxygen  approached 1 mg/l, air was
 admitted  at 10 l/min or 20 l/min, and the dissolved oxygen was continuously measured by an
 oxygen analyzer (Toshiba-Beckman Co.  Ltd., 777 type).

 Oxygen transfer can be expressed by Formula 2, using an overall oxygen transfer coefficient.

                                      dC
                                     — = KLg (Cs-C)                                (2)


 Here, Kj_a = overall oxygen transfer coefficient
    C = dissolved oxygen concentration
    Cs  =  saturated dissolved oxygen concentration

The transfer coefficients computed from the above relationship are shown in Table 3 and Figure
 11. These results show that the oxygen transfer coefficient is affected by temperature. This effect
can be expressed by Formula 3:

-------
                                                                                       273
in which
     T = temperature (° C)
     K|_a T = transfer coefficient at temperature T
     KLa jo = transfer coefficient at 20° C
     0 = temperature coefficient
The temperature coefficient, which is computed from Formula (3), was found to be 1 017 This
value agreed favorably with the result by Eckenfelder (1961).
                        SUBSTRATE
                         STORAGE
            COOLING

            APARATUS
                       AERATION     SEDIMENTATION
                        TANK          TANK

                      (Complete  \    Volum«-63L
                                                         SLUDGE
                                                         RETURNING
                                                         PUMP
                                        LARGE SCALE WATER BATH


                      FIGURE 10  Complete mixing continuous flow units
                                         TABLE 3


                  The Effect of Temperature on Oxygen Transfer Coefficient

                                           Oxygen Transfer Coefficient (I/hour)

                                            10 1/min
   Water
Temperature
                   10° C
                   15° C
                   20° C
                   25 C
                              2.6
                              3.0
                              3.2
                              3.5
                              3.2
20 1/min

  5.2
  6.5
  6.1
  6.9
  7.4
The  ratio of the  mass of oxygen  transfer at  any water temperature to the transfer at 20° C is
calculated from  Formulas 2 and 3,  assuming  the dissolved oxygen  concentration is to be held
constant, for instance, at 2 mg/l. This value, shows, as in  Figure 12, that the  mass of oxygen
transferred increases with water temperature decrement. The  mass  of oxygen transfer is  more

-------
 274
affected  by increasing a saturated  dissolved  oxygen concentration than by decreasing an overall
oxygen transfer coefficient. From this result, there need be no concern that oxygen transfer will
be hampered by a lowering of the water temperature.
                            LJ
                            O
                            O
                            O
                            a.
                            LU
                                                        FLOW RATE
                                                         ZOL/min
                                                        FLOW RATE
                                                          lOL/min.
                                  0   5   10   15   20  25

                                   WATER TEMPERATURE-*C

                  FIGURE 11   Oxygen transfer coefficient and temperature
                  o
                  °
                  e
                  tc.
                  u
                  u.
                  CO
                 LJ
                 CO
                 CO
                 o
                 I
1.2
                      1.0
                      0.9
                        0       5       10       15       20      25

                                    WATER  TEMPERATURE - °C

                        FIGURE  12    Ratio of mass of oxygen transfer

-------
                                                                                       275


 The Effects of Temperature On the Purification Activity of Activated Sludge

 Procedure


 Experiments shown in Table 4 were performed to find the effect of temperature on the activated
 sludge process.
 Run No.

   1-1
   1-2
   1-3

   2-1
   2-2
   2-3
   2-4

   3-1

   3-2
   3-3
   3-4

   4-1
   4-2


   5-1
   5-2
   5-3
Substrate


  sewage

    91


skim milk
skim milk
+ peptone
skim milk
 glucose
                TABLE 4

           Experimental Details

Aeration tank   Aeration period

  M.C.A.T.1           6 hr
      "                »
      "                »»

  C.M.A.T.2
 M.C.A.T.3
Water temp.

   20: c
   15° C
   10° C
   20° C
                                                   15" C
                                                   10° C
   20° c
   15° C
   10° C
    5°C

   20° C
   10° C
                                      20" C
                                      15° C
                                      10° C
   Operation

C.F.,4 1440 1/D
                                                   C.F., 10801/D
                                                   C.F., 1290 1/D
                                                   C.F., 7041/D
                                                                C.F., 1440 1/D
                                                                    Batch
    multi-cell (6 cells) aeration tank
    completely mixed aeration tank
(3) multi-cell (14 cells) aeration tank
(4) continuous flow


Apparatus. The apparatus used in the experiments is shown in Figure 13. A plug flow aeration
tank was used in runs No. 1 and No. 3. This aeration tank was simulated from an actual aeration
tank of a sewage treatment plant by dividing it into multi-cells.


Substrate. The model  plant  (run No.  1), which  was fed domestic sewage, was installed in the
Makomanai  sewage treatment plant. Preclarified  sewage  was used as a substrate, and the model
plant fed  under  load  fluctuation, which  caused only  fluctuation  of  sewage  concentration.
Synthetic sewage (runs No. 2 and No. 3) had ammonium chloride added to supply nitrogen to the
activated sludge.


Operation. Model plants were  normally operated at 1  l/min. inflow and 0.25 l/min. return sludge.
Under these loadings, aeration periods were 6 hours and sedimentation periods 1 hour. However,
when suspended solids were carried over from the sedimentation tank, and  the aeration tank could
not sustain  the  desired activated  sludge  concentration,  the rate of inflow was decreased. The
volume of return sludge was then increased so that the aeration period would remain constant at 6
hours.

-------
 276
Acclimation was performed by increasing an organic load from low values to a set value. Domestic
sewage  sludge was  used for  seed.  Later, to  confirm acclimation, testing was started. Batch
experiments were performed using continuous flow plant sludge.


Analysis. The sample was analyzed for water temperature, pH, dissolved  oxygen, total  residue,
suspended solids, volatile suspended solids, chemical oxygen demand, biological  oxygen demand,
organic  nitrogen, ammonium nitrogen, nitrite nitrogen; nitrate nitrogen and sludge volume index
(SVI) according to the 12th edition of Standard  Methods (1965).


Results and Discussion


The results of continuous flow plants are shown in Table 5 and the results of batch experiments
are shown in Table 6.


Settling Characteristics.  The sludge volume index  (SVI) proved that sludge  settling characteristics
depend strongly on the sewage  temperature, as in Figure 14.

                                       TABLE 5
                             Results of Continuous Flow Plant
 1-1    1-2   1-3   2-1
Water temp.  C
Organic load
MLSS2
SVI
COD2
Org-N+NH3-N2
COD2  ,
CODs3'2
                   20
                 0.25
                 3778
                   90
 286
55.9
  15
 0.35
2995
 178
                6    20
             0.38  0.34
            2836 3035
              181    45
                        346   365   322
                        63.8   67.3   34.4
 Run No.

 2-2    2-3

  20    15
0.56  0.17
866  2336
   -   322

 Influent

152   138
10.0  10.4

 Effluent
                                                         2-4   3-1
                                                          10
                                                        0.15
                                                        2431
                                                         402
                                 233
                                 17.4
                      20
                     0.33
                    2636
                      51
                                                               275
                                                               27.5
  3-2

  15
0.47
1000
 112
                            157
                           15.7
  3-3   3-4

  10     5
 0.25  0.14
2647 3219
 345   250
        161
       16.1
 Org-N2,
 NH3-N2
 NOj-N2
 NO3-N2

 COjD removal


 COD removal5
 Org-N+NH3-N
 removal %

NO2-N-t-NO3-N
removal %

Nitrification
Activity6

 1) Organic load = kg COD/kg MLSS/day
 2) Concentration = mg/1
 3) CODs = Soluble COD
                   14
                                           135   145
                                        58
                                         17
                                                                       17
                                                            19
                                           6-g    2.JJ     l.g    0.7    1.1     0.
                                                xlO"4  xlO   xlO    xlO'^  xlO"
        147
       14.7
83
45
43
2.1
18.6
7.2
1.4
71
89
327
63
45
31
22
1.8
34.6
3.3
1.2
87
91
414
43
274
37
209
17.6
35.5
0
0
25
90
128
22
51
31
23
-
- .
-
85
91
394
-
7.1
1.1
2.1
11.4
.
-
.
18
9
8
26
1.2
0.2
0.2
14.9
93
94
167
87
115
13
117
15.8
7.8
0
7.1
51
94
83
0
52
17
51
2.6
8.9
0.36
4.4
81
96
292
58
27
11
11
2.6
7.5
2.1
0.7
83
93
188
29
26
9
15
4.6
2.3
0
3.2
83
94
192
57
45
7
32
1.2
3.8
0
0
69
96
144
53
                                           0


                                           0
                       '*  xlO'2  xlO"12

'4) Calculated from CODs
,5) COD removed = g COD/day
^6) Nitrification activity = (N02 -N+NO3 -N) MLSS day

-------
                -600-
     o
     »
                   AIR
         M50-»f-	3OO-
                                                                                 277
                                 INFLOW [
                                      RETURN SLUDGE
T+

•0

LU
z
1


10
^




10
r-




_i
*•




_i
£>




¥ U
_i
r-


1

-------
278
                                            HEATER
                                DIFFUSER
                                             FLOW METER


                                  FIGURE 13-3  Batch unit
 Here, e = void ratio
     Re =  Reynold's number
     A = coefficient of flow properties

 Figure  15 shows  the  change of SVI  and substrate concentration after  substrate contact with
 activated sludge. SVI increased in gradual proportion to absorbed substrate and showed maximum
 values at the time when substrate was almost removed from the solution. Afterward, SVI gradually
 decreased with  the utilization of absorbed substrate. Therefore, it was considered that SVI was
 related to the absorbed substrate.

 It is considered from the above  description that the high value of SVI at low water temperature is
 not only  attributable  to change of  water viscosity but also to changes of activated sludge floe
 physical  properties like density,  bound water  ratio, and  surface electric  charge.  Further
 investigations into these relationships between the biological and physical properties are necessary.

 COD.  The removal  ratio of  soluble COD was  not affected, but COD that contained suspended
 matter was affected, by water temperature in a continuous flow aeration unit, as in Figure 16. This
 showed an  increase of suspended matter, carried  over from the sedimentation tank in low water
 temperatures. Total mass of COD removed decreased with water temperature, as in Figure 17. This
 was the result of floe  carry-over at the Makomanai model plant; other model plants were operated
 under low organic load to repress the high SVI or low overflow rate of the sedimentation tank to
 prevent floe carry-over.

-------
                                                                                     279
    Water temp.

   Organic load*
    MLSS mg/1

COD initial (mg/1)**
COD 6 hrs (mg/1)
                                        TABLE  6
                               Results of Batch Experiments
K

4-1
20° C
0.34
3500
278
54
2.5
xlO
xibOJ*



0.18
3500
139
49
2.2
xlO
6.5g



0.40
3000
286
44
0-9
xlO"2
4.08
xlO'*

Run No.
4-2
10° C
0.30
2000
66
18
l^

3.72
xlO"4


5-1
20° C
0.18
2200




8.7
xlO4
3.9
«ir» *

5-2
15° C
0.18
2200




xlO:?
2 3

5-3
10° C
0.18
2200




xlO^
14
 •Nit.
*  Organic load = kg COD/kg MLSS/Day
**  COD initial was determined after 3 min. of aeration K = I/day
The removal of COD is shown in Formula 5:

                                       dL
                                       dt
Here, L  = substrate concentration
    S =  initial activated sludge concentration
    K = substrate removal rate
                                           = - KSL
                                  (5)
                                400

                                350

                                300

                                250

                            -   200
                            CO
                                150

                                100

                                 50

                                  0
O  RUN  No I

X  RUN  No. 2

   RUN  No. 3
                                       5    10    15   20

                                      WATER TEMPERATURE-"C

                           FIGURE 14 SVI and water temperature

-------
280
Soluble COD removal rate in batch tests (Table 6) showed it decreased with sewage temperature.
Temperature coefficient (6) which was obtained according to Formula 6 is 1.089.
                                                                                         (6)
Here. KT = the rate at T° C
                         °
         = the rate at 20° C
    T = water temperature
    6  = temperature coefficient

This (0) showed that the removal rate was about half when the water temperature was decreased
by 10° C.  Figure 16 shows that the removal rate was not affected by temperature in a continuous
flow aeration tank as in the batch experiments. This was due to the effluent of continuous flow,
sampled after 6 hours of aeration.

There  is a  relationship between settling characteristics and  absorbed substrate of activated sludge
that is shown  in Figure 15. And the removal  rate is affected by absorbed substrate of return
                                                                  - 300
                   ef
                   o
                   u
                                                                  - 200
                                                                        >
                                                                        n
                                                               12
                                   AERATION PERIOO-hr
                          CONDITION OF EXPERIMENT
                                 Wofcr temperoiure « 20»C  Substrate • skim milk, peptone
                              A- Organic load « 0.50 kq
-------
                                                                                       281
sludge. From these points, it is assumed that the stabilization time for oxidation or synthesis of
absorbed substrate  (that  is,  the  aeration  time after the removal by absorption) is the key to
successful operation of the activated sludge process.

Nitrogen. The primary nitrogen components of influence to sewage  treatment plants are organic
nitrogen  and ammonium  nitrogen. These components are used by bacteria and converted to  cell
nitrogen  or  to  nitrite and nitrate nitrogen. Nitrification  is very sensitive to dissolved oxygen in
mixed liquor, so results  in Tables  5 and 6 are from  experiments  performed above 3  mg/l of
dissolved oxygen.

The results  of  batch  units (Fig.  18} show that the organic and ammonium nitrogen removal are
first order reactions, expressed by Formula 5, and nitrification is a zero order reaction, shown by
Formula 7.
                                         dt
                                             = KS
(7)
Here, L =  nitrite and nitrate nitrogen
    S = mixed liquor suspended solids
    K = rate of nitrification

The removal rates of organic  and ammonium nitrogen and the rate of nitrification (Table 6),
determined according to Formulas 5 and 7, show that these rates decrease with temperature. The
temperature coefficient (9)  according to Formula 6 is 1.092 for organic and ammonium nitrogen
and 1.106 for nitrification.

The experimental  results of continuous flow plants in Figure 19  show the same phenomena as in
municipal sewage treatment plants of the same organic load. When the temperature is decreased to
5°  C, nitrification does not occur and the  nitrogen compounds in  the influent are discharged
without stabilizing.


T
o
i
_j
5
2
UJ
Lt
0
s



100
90
80
TO

GO
50

40
30
20
10
0
COD
v*-*^.
*x>/!/"xb

// O RUN Na '
'
/ X RUN No. 2

/ • RUN No 3
d
— •— TOTAL COO
— O~ SOLUBLE COO

                                          5    10   IS   20

                                          WATER TEMPERATURE-«C

                      FIGURE 16 COD removal ratio and water temperature

-------
 282
From the above, the  rate coefficient of nitrogen removal or nitrification  is smaller and more
sensitive to temperature than that of COD, The nitrogen removal reaction is not completed in 6
hours of aeration as is COD,  and the nitrogen compounds in the influent are discharged with
partial or no stabilization from the aeration plant.
                           a
                           o
                           o
                               400
                               300
                               200
                               100
                                 0    5   10   15    20

                                    WATER  TEMPERATURE-*C
                  FIGURE 17 Mass of COD removed and water temperature
                                                   WATER TEMP
                                                     20* C
                                                    WATER TEMP
                                0     48     12

                                  AERATION PERIODS- HOUR

              FIGURE 18-1  Effect of water temperature on nitrogen decrement

-------
                                                                       283
                IT19/I
                 0     4      8      12


                    AERATION PERIODS-HOUR
 FIGURE 18-2  Effect of water temperature on nitrogen removal
          I
          UJ

                                     O  RUN No. I


                                     X  RUN Na2
                                         RUN No. 3
                     5   10   15   20


                   WATER TEMPERATURE -»C
FIGURE 19 Nitrogen removal rate and water temperature

-------
 284


                                      CONCLUSIONS

 The following conclusions have been reached from these studies:

 1.   At low temperatures, the oxygen transfer coefficient in the aeration tank decreases, but the
     mass of oxygen transfer increases slightly with the lowering of temperature.

 2.   Sludge volume index increases at low temperatures. It creates a high COD effluent.

 3.   The value  of SVI changes with time after substrate contact with activated sludge. At a low
     sewage  temperature, it is necessary to take  sufficiently prolonged aeration time to stabilize
     the activated sludge which absorbed substrate.

 4.   The removal ratio of soluble COD is not affected by a decrease of sewage temperature, but
     total COD of effluent increases due  to an increase of suspended matter.

 5.   The rate of removal of soluble COD varies with water temperature. This relationship is shown
     in Formula 6, and the temperature coefficient is 1.089.

 6.   Nitrogen removal is  influenced remarkably  by temperature. The rate of removal of organic
     and ammonium nitrogen and the rate of nitrification are shown by Formula 5 and Formula 7
     respectively. These rates decrease with lower temperatures, and temperature coefficients are
     larger than that of removal of COD. This is the reason the effluent of low sewage temperature
     contains high nitrogen.

                                  ACKNOWLEDGMENT

 A part of this research was supported by a scientific research grant of 1969 from the Department
 of  Education of Japan.  The City  of  Sapporo  supported this study with convenience and
 expenditure.

                                      REFERENCES

 Banerji, S. K. (1965) Biological removal  of colloidal waste in activated sludge process, Ph.D. thesis
     of U. of Illinois.

 Eckenfelder, W. W. and O'Connor, D. J. (1961) Biological Waste Treatment, Pergamon Press.

 Keefer, C. E. (1962) Temperature and efficiency  of the activated sludge process J W P C F Vol
     34.                                                                '

 Ludzack, F. J.,  Schaffer,  R. B. and Ettinger, M.  B. (1952) Temperature and feed as variables  in
     activated sludge performance, S.I.W., Vol. 24.

Okun,  D. A. (1949) System of bioprecipitation of organic matter from sewage, S.W.J., Vol. 21.

Sakai, T.  (1963) A study of the snow-melt runoff of rivers (Japanese), Transactions J.S.C.E No
     95.

-------
                                                                                    285
Standard Methods (1965) 12th edition.

Tanbo,  N. and  Abe, S. (1969)  Behaviors  of floe  blankets in  a upflow clarifier (Japanese),
     J.J.W.W.A., No. 415.

-------
            MICROBIOLOGIC  INDICATORS OF THE EFFICIENCY
                OF  AN AERATED,  CONTINUOUS-DISCHARGE,
                SEWAGE  LAGOON  IN  NORTHERN CLIMATES
                           John W. Vennes and Otmar 0. Olson
                                   INTRODUCTION

Sewage stabilization lagoons have been used in the United States as a method of waste treatment
for the past 20 years. The first designed sewage stabilization lagoon in North Dakota was approved
by the State Department of Health in  1948 (Van Heuvelen, et al., 1960). The design criteria
established for this system were much the  same  as present standards of 20 Ibs. BOD5/acre/day
with a minimum of 100 days retention for winter storage.

The  BOD5 loadings that can be adequately stabilized under aerobic conditions, with oxygen by
algal  photosynthesis  being  the  primary contributor to aerobiasis, depend on solar  radiation,
temperature, sewage characteristics, wind action and depth. Temperature and solar radiation are of
prime consideration as regards the growth of algae and bacteria. Mixing and distribution of waste
in a conventional  lagoon are primarily dependent upon wind  action. A common problem in
conventional lagoons occurs during the first warm days in  the spring when anaerobic conditions
prevail due to benthic deposits rising to the upper layers of liquid. The recognition of problems
encountered in maintaining aerobic conditions in these conventional lagoons led to the application
of artificial aeration.

The  aerated lagoon  is one of the most recent developments in the biological waste treatment
system. This concept was initially developed to supplement oxygen during the period of  spring
break-up  by  artificially aerating  stabilization ponds.  Lagoon  aeration  technology  has  been
developed to the  point where aerated lagoons are now designed for complete waste treatment
(Sawyer, 1968).

                                      METHODS

The  city of Harvey,  North Dakota, treats its domestic waste in an aerated lagoon system. The
system consists of two cells, each having a water surface area of 1% acres. The cells are designed to
operate in series, each providing a 20-day retention time. The dikes have a 3 to 1 slope and support
a 10-foot berm, which allows the complete system to be constructed in less than 6 acres. Overflow
manholes  in  the two  cells   allow  them  to   be operated  at  a  10-foot depth with  a
continuous-discharge  to the Sheyenne River.

The  aeration system consists of two 15 hp Sutterbilt blowers, each capable of providing 270 cfm
at 9 psi. The air is distributed to the two cells through a plastic header pipe paralleling the cells
with weighted diffuser tubes connected to the header. There are 78 diffuser lines distributing air
into  the primary cell  and 40 lines in the second cell, giving a total of over 15,000 feet of tubing
disbursing the  air. The equipment was supplied by Hinde Engineering Company, Highland Park,
Illinois, and is known as an Air-Aqua System.
                                         286

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                                                                                      287
The blowers are operated alternately with a time clock to assure continuous operation of the waste
treatment facility. The blowers have been in essentially continuous operation since October 1965.

Ice cover usually  is seen  in the secondary cell  in November or early December while the primary
cell does not show ice cover until late December or early January.

The primary cell was  designed to be loaded at approximately 400 Ibs. of 5-day biochemical oxygen
demand (BODs)/acre/day and the secondary cell at about 100 Ibs. of BODS/acre/day. Each cell
has a detention time of about 20 days.

Sampling Procedure

Sampling of 24-hour composite raw city waste and effluent from the primary and secondary cell
manholes was  carried out during the period from January 1966 through June 1969. Daily flows of
sewage  averaged  175,000 gpd with changes occurring during  spring run-off and rainy weather.
Samples were  usually collected on a monthly basis, however, on occasion two samples were taken
during the same month. Since this facility  is about 150 miles from the laboratory, the  samples
were maintained at approximately lagoon temperature in an insulated container and transmitted to
the laboratory the same day. Microbiologic determinations were carried out immediately on arrival
at the laboratory  while the determinations for other parameters were made either the same day or
the following morning. Samples in the laboratory were maintained  at 5° C prior to the following
day determinations.

Laboratory Determinations

Determinations for coliform, fecal coliform, and enterococci were  made by  the Millipore filter
technique while the total bacteria populations were enumerated with tryptone-glucose extract agar
(Standard Methods,  1965). The determinations for BOD5, total and suspended  solids,  pH and
Kjeldahl nitrogen  were made  according to Standard Methods (1965). A few determinations were
made for biotin by the bacteriologic assay method (Wright and Skeggs, 1944) with Lactobacillus
plantarum. Several determinations for sulfide and phosphate were also made by using Standard
Methods (1965).

                                        RESULTS

Laboratory determinations for BOD5, Kjeldahl nitrogen, pH, total and suspended solids, coliform,
fecal  coliform, enterococci,  and total  bacteria are  tabulated  in the Appendix   (Tables 5-12).
Graphic presentation of this data is seen in Figures 1 through 6.

This  aerated lagoon  discharged its effluent continuously into a water course; therefore it was
considered useful  to determine the mean values for several parameters monitored during the period
of the study. It can be seen in Table 1 that  the mean BOD5 for the period was 53 mg/liter (S.D.
±45 mg/liter).  The suspended solids show a mean value of 67 mg/liter (S.D. ±39 mg/liter). Mean
nitrogen shows values of 7.7 mg/liter (S.D. ±3 mg/liter). There was considerable variation in the
composite raw samples in that the mean BODS of the 24-hour composite raw was 332 mg/liter
(S.D. ±422  mg/liter).  It is  thus apparent that the loading on the primary cell changed rather
drastically during  the period of the study due primarily to a milk plant.

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 288
                                        TABLE  1
                     Statistical Correlation of Several Lagoon Parameters
                                                           mg/liter

Parameter                                Raw               Primary             Secondary
BODS                Mean            332(263)*                126                    53
                     S.D.             422(134)                 76                    45

TVS                 Mean            567(496)                401                   353
                     S.D.             424(118)                 94                    98
VSS                 Mean            191(166)                118                    67
                     S.D.             168(118)                 74                    39
N2                   Mean            20(15.5)               11.2                   7.7
                     S.D.              27(5.3)                 3.8                   3.0
"Value obtained by disregarding one apparently non-representative sample.

An attempt was made to assess the effect of changing loadings and temperature on this lagoon by
comparing BODS values with coliform, fecal coliform, enterococci, and total bacteria. Figures 7
through 9 display this relationship on a log-log basis and suggest that microbial populations in the
secondary lagoon are directly related to the BODS  or total loading.

Correlations of the lagoon parameters tabulated during the different periods of the study, namely,
for the complete sampling period, for the months when the lagoon liquid temperature was near 0°
C (i.e. January through March), and the period when the lagoon was near 10° - 20° C (i.e. June
through  September) are displayed  in Table  2.  It can be noted in this table  that there  is a
reasonably good correlation between the BODS and the Kjeldahl nitrogen during all periods of the
test. One may also observe that the BODS  of the  secondary lagoon, during times when the lagoon
temperature was near 0° C, showed excellent correlation with coliform and fecal coliform bacteria.
Less correlation was seen with the enterococci and BOD5, and little correlation was noted between
BOD5  and total bacteria. During the summer months, when the lagoon temperatures were between
10° and 20° C, the  relations between BODS and coliform, fecal coliform, and enterococci were
less attractive. There was, however, during this time period, a reasonably good correlation between
the secondary lagoon BODS and the total bacterial population.

The relations between nitrogen and coliform, fecal coliform, and enterococci during the winter
months of  January  through March showed excellent correlation; however, the total bacterial
population does not  show a direct relation to the total nitrogen in the secondary lagoon. Again, as
with the BODS and microbial numbers at 10° - 20° C, there is little correlation between the total
nitrogen  and enteric bacteria at summer temperatures. There is some correlation between total
nitrogen and total bacteria during the summer months.

One of the apparent difficulties with the aeration system, as utilized in this continuous-discharge
lagoon, is the fact that precipitation of insoluble salts tends to decrease the porosity in the diffuser
tubes and  pressures tend  to  build  jn  the  system. Occasional cleaning of the  system with
hydrochloric acid to  solubilize the salts usually relieves the pressure and increases the pore size. It
was noted during the treatment year from January  1966 through January 1967 that excellent
reductions  in  BODS were  obtained  in the lagoon.  However, during the treatment year  1967

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                                                                                       289


                                          TABLE 2

                      Correlation Coefficient of Several Lagoon Parameters

  Parameters Compared                            Correlation Coefficient
                                                   Months compared
                                     A11               Jan. - Mar.               June - Sept.
  BOD-nitrogen                     0.89                 0.89                     0.82
  BOD - coliform                     0.33                 0.93                     0.10
  BOD - fecal coliform                0.13                 0.93                     0.31
  BOD - enterococci                  0.73                 0.70                     0.19
  BOD - total bacteria                0.52                 0.35                     0.79
  Nitrogen - coliform                 0.48                 0.91                     0.20
  Nitrogen - fecal coliform            0.12                 0.96                     033
  Nitrogen - enterococci               0.41                 0.90                     053
  Nitrogen - total bacteria             0.43                 0.17                     0 29
 through 1968 a cyclic effect in the secondary  lagoon  parameters  was noted and  decreased
 efficiency  (due  to apparent lack of delivered oxygen) resulted in rather large amounts of BODS
 and microbial numbers being discharged to the water course. For example, during the months of
 January through March in  1968 there was approximately a two-fold increase in the nitrogen and
 suspended  solids in  the secondary lagoon. There was nearly a four-fold increase in the BODS.
 There was  also an increase of from 1 to 2 logs in the coliform, fecal coliform, and enterococci in
 the secondary effluent. No consistant increase in the total bacterial population was detected.

                                       DISCUSSION

 Two of the  most important physical  factors in  this continuous-discharge  lagoon affecting the
 stabilization  of  organic molecules, and hence microbial growth, appear to be temperature and
 delivered oxygen.  Since two of the other parameters related to microbial growth are substrate
 availability and pH, and since it is assumed that raw sewage will usually support adequate growth
 of microorganisms for near complete stabilization of the  organic species present, and since pH
 varied  little  from  neutrality, the  major  concern with  lagoon efficiency  must remain with
 temperature and oxygen.


This study allows the  determination  of  these  effects  of  temperature and oxygen on biologic
stabilization and reflects these findings  in the relative abundance of several microbial  species and
BODS.  For example,  it was  noted  that at near 0° C the total microbial population did not
correlate well with BOD5 reductions, while reductions in coliform, fecal coliform, and enterococci
were directly  related to the  BODS  of the  supporting medium. Initial populations of enteric
organisms were thus determined by  the strength of the raw sewage. This relationship does not
remain  during summer temperatures of 10° -  20° C. It  would thus appear that the rates  of
utilization  of  lagoon substrates by  enteric  organisms  are different at  different temperatures.
However, since the total microbial population varied little at different  BODS  loadings it may be

-------
290


that changes or die-off rates of coliforms may represent primarily the variable of time. Alternately
it may be that BOD5 is not a useful parameter in assessing relations of enteric organisms to organic
loading.

In order to verify the assumption that temperature, pH, and substrate availability did not prevent
microbial oxidation it appeared useful to compare those periods when the lagoon was known to be
at or very near 0° C with those times when it was at 10° - 20° C (when the reduction in organic
species, as reflected by the BOD5, is expected to be at its most active level).

The mean BODS  of the raw composite waste during the months of January through March in the
years of 1966, 1967, and 1969 was 312 mg/liter (S.D. ±180 mg/liter), while the effluent from the
secondary cell had a mean BODS of 50 mg/liter (S.D. ±23 mg/liter). Assuming flows to average
175,000 gpd, then, as seen in Table 3, about 445 Ibs BOD5/day were loaded in the primary cell
and about 188 Ibs BODs/day were loaded in the secondary cell. A reduction of 84% in BODS was
thus noted for a period when temperatures were near 0° C.

The mean BOD5 of the raw composite waste during the months of January through March in  1968
was 665 mg/liter (S.D. ±950 mg/liter), while the effluent from the secondary cell had a mean of
160 mg/liter (S.D. ±19 mg/liter). Thus the loadings on the primary cell were about 970 Ibs
BODs/day, while  329 Ibs BODs/day were loaded on the secondary cell. An overall reduction of
75% was obtained in the total BODS.
                                      TABLE 3

            Loadings in Primary and Secondary Aerated Lagoons at Various Times

                                           Loadings (Pounds BODj/day)
   Year/s
  (months)

 1966-67-69
 (Jan - Mar)

    1968
 (Jan - Mar)

     All
 (Jan - Sept)

     All
    (All)
1966-67-69
 (Jan - Mar)

   1968
 (Jan - Mar)

    All
(Jun - Sept)
 Primary

   455

   970

   408

   485


   Raw

312 (±180)

665 (±950)

280 (±117)
 Secondary

    188

    329

    136

    265

BODS (mg/1)

  Primary

 129(±10)

 226(±65)

  93(±28)
 Effluent

    73

   233

    41

    78


Secondary

 50 (±23)

160 (±19)

 28 (±23)

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                                                                                      291


However, during January through March in 1968, an average 737 Ibs BOD5/day were removed by
the aerated cells, while during the other years studied a mean of 382 Ibs BODs/day were removed.
Of course some of the removal of BODS  in the primary cell was probably due to sedimentation,
and comparing the secondary cell removal rates may be more relevant to  this study. In 1968 the
secondary cell removed an average of 115 Ibs BODs/day, while during the other years of the study
a mean of 96 Ibs of BODs/day were removed  during  the January through March time period, tt
appeared at this point that temperature  did not determine the rate of removal of BODS, since
about equal amounts were removed during all time sequences in the secondary cell at or near 0° C.

The mean BOD5 of the raw composite waste during the months of June through September for all
years studied was 280 mg/liter (S.D. ±117 mg/liter), while the effluent from the primary cell had a
mean  of 93 mg/liter BOD5 (S.D. ±28 mg/liter) and  the secondary  cell effluent showed  a mean
BOD5  of 28 mg/liter (S.D. ±23 mg/liter). Therefore during this time period the primary cell was
loaded at 408 Ibs BOD5/day and the secondary cell at 136 Ibs BODs/day with 41  Ibs BOD5/day
being discharged to the water  course. Overall reductions in BODS  were about 90%, with 67%
occurring in the primary cell. It is interesting to note that the secondary cell of this aerated lagoon
removes between 95 and  115 Ibs BOD5 at all temperatures. Thus, as suggested above, temperature
was not the limiting parameter in total BOD5 reduction.

The aeration system used in this continuous-discharge lagoon utilizing a 15 hp blower at 270 cfm
at 9 psi delivers oxygen  sufficient to satisfy approximately 375  Ibs BOD/day (367 to 382  Ibs
BOD/day range) at all temperatures. Thus the system is capable of removing approximately 1 Ib of
BODs/HP hr. Loss of efficiency in the system  by decreased  porosity  in  the plastic tubing is
probably not as important as  the  lack  of  diffusibility  inherent in the design of the system.
Additional  oxygenation transfer  will  be required to determine the ultimate efficiency  of this
system at higher temperatures. It may be that  at 0° C the maximum efficiency has already been
established by the data presented in this report. If this  proves to be a fact, then a basis for aeration
capabilities of these  lagoons has been further validated.

Allowing the assumption  that the maximum efficiency for this system has been established, then
coliform, fecal  coliform, and enterococci reflect reasonably well the biological degradation of
organics at 0° C as contrasted to summer temperatures (10° - 20° C) where little or no correlation
exists.  Additional parameters will need to be  investigated in order to determine those reactions
that better reflect the biologic reactions that occur at all temperatures. Since only 1% or less of the
total microbial population  present in the lagoon is represented  by the enteric organisms studied
here, it is apparent that other organisms must be studied to better define the role of microbiologic
indicators in the efficiency of this sewage treatment system.

One system is being studied  in our laboratory which relates to several organisms that thrive in
sewage oxidation  lagoons.  It is concerned with the  production  and  utilization of the B vitamin,
biotin.

We have found  (Fillipi and Vennes, 1970) that biotin is produced by a number of  enteric
organisms, Aerobacter aerogenes being one of the  most productive. Utilization of the vitamin
seems to be limited to photosynthetic organisms  (although some bacteria have been reported to
utilize  or at least degrade biotin) and in our study Chlorella and probably other algae and several
species of purple sulfur bacteria seem to be the most active.

-------
 292
 Although production of the vitamin has not been established to be directly related to organic
 loading of the lagoons, utilization seems to be associated with the production or growth of algae.
 Data are not sufficient at this time to present a definitive outline of these relations, although Table
 4 shows the tabulations in lagoons in eastern North Dakota. It is apparent that no good correlation
 exists between BOD5 and biotin in these lagoons. Rather it is suggested, based on our previous
 findings (Fillip! and  Vennes,  1970), that the  precursors  for biotin production  are present in
 lagoons in different amounts and growth of biotin-producing organisms predominate on this and,
 we expect, other bases. Utilization however seems to be limited primarily to the presence of algae
 and thus disappearance of biotin may prove to be directly related to algal numbers.

                                       TABLE 4
    Date
  9 Apr 69

  5 Jun 69

 21 Apr 69
 21 May 70
  5 Jun 70
  5 Jun 69
 10 Jul 69
 26 May 70
 20 May 70
  3 Jun 70
 20 May 70
  3 Jun 70
 20 May 70
  3 Jun 70
14 May 69
11 Jun 69
25 Jun 69
10 Jul 69
 7 Aug 69
                   Biotin and BOD5 Relations in Several Oxidation Lagoons
          Source
 Harvey I	
 Harvey Secondary
 Harvey L __„	
 Harvey Secondary
 Grand Forks Secondary - £
 Grand Forks Secondary - W
 Grand Forks Secondary - E
 Grand Forks Secondary - W
 Grand Forks Secondary - E
 Grand Forks Secondary - W
 Lakota Secondary
 West Fargo Secondary
 East Grand Forks Secondary
 Crookston Secondary - W
 Crookston Secondary - W
 Crookston Secondary - E
 Hillsboro Secondary
 Hillsboro Secondary
 Northwood Secondary
 Northwood Secondary
 Grafton Secondary
Grafton Secondary
Grafton Secondary
Grafton Secondary
Grafton Secondary
BODS
(mg/1)
   27
   33
   58
   56
  119
   82
  166
   82
   91
   39
   12
   43
   35
  310
  166
  331
   20
   37
   27
   30
  513
  460
  180
  169
  156
Biotin
(ng/1)
    10
    20
    22
  134
  326
  120
 1720
 2070
 2200
 1950
    18
   53
   24
 2275
 2950
 2840
   72
  284
   22
   83
  936
 3530
 8500
  670
   32

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                                                                                     293


It is suggested then that although BOD5  and total bacterial numbers are somewhat indicative of
utilization of organic  substrates in lagoons, more  sophisticated studies are needed to interrelate
microbial  numbers and organic constituents  responsible for stabilization  of  wastes. Biotin
production and utilization may be an example of the latter relationship.

                                        SUMMARY

1.  The limiting parameter in BOD5 reduction in an aerated, continuous-discharge lagoon in North
Dakota appears to be delivered or utilizable oxygen. No difference in BOD5 reduction was noted
in the secondary lagoon at temperatures varying from 0° to 20° C.

2,  Coliform,  fecal coliform and enterococcal numbers in the secondary lagoon during winter
temperatures of near  0° C were directly  related  to BODS  and total  nitrogen. During summer
temperatures little correlation between these enteric organisms and BODS and total nitrogen was
noted. However, there was  a correlation between the total microbial  population and BODS  at
summer temperatures.

3.  Although the physical aspects of the aeration system can apparently be improved by additional
engineering, the understanding of the biologic system will  require extensive study of specific
ecologic relationships in the lagoon (biotin production and utilization were used to illustrate the
complexity of this system).

                                  ACKNOWLEDGMENTS

The technical assistance of  Janice Granum and Gordon Fillip! is gratefully acknowledged. The
continuing  interest  and assistance from  the  North Dakota State  Department of  Health and
particularly Raymond  Rolshoven is also acknowledged.

This investigation was supported in part by the  North Dakota Water Resources Institute with
funds provided by the U. S. Department of Interior, Office of Water Resources Research under P.
 L. 88-379.

                                       REFERENCES

 Fillipi, G. M. and Vennes,  J. W.  (1970) Biotin  production and  utilization in certain natural
     environments, Bact. Proc., p. 18.

Sawyer, C. N. (1968) New concepts in aerated lagoon design and operation. Adv. in Water Quality
      Improvements, 1:325-335.

Standard  Methods for the  Examination  of Water and Wastewater, 12th ed., Orland, H. P. (ed.)
      Amer. Pub. Health Assoc., Inc., New York.

 Van Heuvelen. W., Smith, J. K. and Hopkins,  G. J. (1960)  Waste stabilization lagoons - design,
      construction  and operation practices among Missouri basin states, J.W.P.C.F., 32:909-917.

 Wright. L. D. and Skeggs,  H. R. (1944) Determination of biotin with Lactobacillus arabinosus.
      Proc. Soc. Exp. Biol. Med., 56:95-98.

-------
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                  FIGURE 1   BODS changes in raw-composite, primary and secondary aerated lagoons

-------
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                    FIGURE 2   Total nitrogen changes in raw-composite, primary and secondary aerated lagoons
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-------
                                     303
APPENDIX

-------
304
                                   TABLE 5


                         BODS Changes in Aerated Lagoons

                                            BOD 5 mg/liter

Date                      Raw                 Primary                 Secondary

15 Nov 65                                                                 25
14 Dec 65                                        154                      16
11 Jan 66                  294                   104                      22
 1 Feb 66                  692                   167                      44
 8 Feb 66                  150                   146                      48
15 Mar 66                                        49                       52
29 Mar 66                                        35                       20
11 May 66                                        104                      29
 6 Jun 66                                        102                      13
22Jun66                  476                   141                      27
18Jul66                                        72                       8
10Aug66                                        75                       18
21 Sep 66                  335                   155                      95
 2 Nov 66                  275                   103                      32
 7 Dec 66                  436                   177                      40
HJan67                  309                   209                      69
 9 Mar 67                  262                   219                      96
22 Mar 67                  308                   172                      57
19 Apr 67                  309                   146                      55
23Aug67                  263                   77                       30
 6 Sep 67                  198                   97                       26
20 Sep 67                  221                   76                       18
 3 Oct 67                  245                   90                       17
18 Oct 67                  165                   69                       23
 1 Nov 67                  240                   96                       23
15 Nov 67                  440                   102                      24
29 Nov 67                  295                   96                       29
13 Dec 67                  320                   181                      73
27 Dec 67                 2600                   193                     109
10 Jan 68                  240                   215                     154
24 Jan 68                  310                   222                     137
 7 Feb 68                  360                   207                     180
20 Feb 68                  345                   350                     178
 5 Mar 68                                        210                     150
12 Mar 68                  140
27 Mar 68                  84                    154                     128
10 Apr 68                  62                    130                      71
24 Apr 68                  56                    129                      74
 8 May 68                  53                    110                      60
20 May 68                  171                   87                       40
 5 Jun 68                  119                   112                      25
19 Jun 68                  348                   89                       12
30 Jul 68                                        90                       17
27Aug68                                        70                       24
 2 Oct 68                                        82                       37
 6 Nov 68                                       400                      19
 9 Dec 68                                        52                       20
14 Jan 69                                        47                       24
21 Feb 69                  167
27 Mar 69                                        48                       39
 9 Apr 69                                        27                       33
 2 May 69                                        31                       8
 5 Jun 69                                        58                       56

-------
                                                                                    305



                                        TABLE  6

                         Total Nitrogen Changes in Aerated Lagoons

                                                 Nitrogen mg/liter

Date                         Raw                    Primary                   Secondary

14 Dec 65                                             14 7                       50
11 Jan 66                    17.0                     12.6                       69
 1 Feb 66                    29.2                     13.7                       7.4
 8Feb66                    12.8                     10.9                       6.9
15 Mar 66                                              46                        53
29 Mar 66                                              6.9                        3.8
11 May 66                                             11.8                       4.0
 6 Jun 66                                              9.1                        4 6
22 Jun 66                    24.3                     10.3                       5.5
18 Jul 66                                               2.9                        3.4
10Aug66                                              4.0                        3.8
21Sep66                    14.1                     17.5                       11.8
 2Nov66                    15.4                     13.7                       9.5
 7 Dec 66                    24.7                     17.5                       6.7
11 Jan 67                    14.8                     16.3                       9.9
 9 Mar 67                    16.7                     12.0                       12.2
22 Mar 67                    18.6                     12.0                       12.2
19 Apr 67                    17.3                     10.3                       8.4
23Aug67                    13.1                     11.2                       7.6
 6Sep67                    12.7                     12.7                       7.2
20Sep67                    11.8                     10.3                       4.9
 3Oct67                    13.9                     11.8                       5.9
18Oct67                    11.8                      8.7                        5.3
 lNov67                    11.6                     13.3                       5.3
15Nov67                    19.8                     14.1                       5.5
29Nov67                    20.7                     13.1                       6.3
13 Dec 67                    16.7                     14.3                       8.7
27 Dec 67                    169.0                    15.0                       12.2
10 Jan 68                    15.0                     14.3                       16.2
24 Jan 68                    19.6                     12.5                       12.5
 7 Feb 68                    18.4                     12.7                       12.4
20 Feb 68                    22.2                     13.6                       13.6
 5 Mar 68                                             11.6                       12.2
12 Mar 68                    13.8
27 Mar 68                     6.8                       9.6                        9.6
10 Apr 68                     7.2                      12.8                       9.0
24 Apr 68                     5.8                      11.0                       9.2
 8 May 68                     6.6                       8.8                        7.8
20 May 68                    15.8                      8.8                        8.2
 5 Jun 68                    12.0                     10.2                       5.4
19 Jun 68                    17.2                      9.8                        6.0
30 Jul 68                                              11.2                       5.6
27Aug68                                             14.8                       9.2
 2 Oct 68                                              9-4                        9.2
 6Nov68                                             12.0                       5.8
 9 Dec 68                                              9.6                        4.8
14 Jan 69                                              9.2                        5.8
21 Feb 69                    13.6
27 Mar 69                                              7.6                        6.6
 9 Apr 69                                              6-4                        6.4
 2 May 69                                              7-0                        3.0
 5 Jun 69                                             14.2                       10.0

-------
306
                                       TABLE 7
                              pH Changes in Aerated Lagoons

                                                      PH

Date                         Raw                   Primary                   Secondary

15Nov65                                                                         7.9
14 Dec 65                                             7.7                         7.7
llJan66                     8.4                      7.6                         7.7
 !Feb66                     7.5                      7.5                         7.7
 8Feb66                     8.3                      7.7                         7.6
15 Mar 66                                             7.4                         7.7
29 Mar 66                                             7.4                         7.4
11 May 66                                             7.8                         8.0
 6 Jun 66                                             7.9                         8.1
22Jun66                     7.4                      7.9                         8.1
18Jul66                                             7.8                         7.8
10Aug66                                             7.7                         8.0
2lSep66                     7.8                      8.0                         8.1
 2Nov66                     8.1                      7.7                         7.9
 7 Dec 66                     8.5                      7.6                         7.6
llJan67                     8.2                      7.7                         7.7
 9 Mar 67                     8.5                      7.5                         7.5
22 Mar 67                     8.2                      7.5                         7.4
19 Apr 67                     8.3                      7.5                         7.6
23Aug67                     7.9                      8.2                         8.4
 6Sep67                     8.0                      8.1                         8.2
20Sep67                     8.1                      8.0                         8.1
 3Oct67                     7.5                      7.7                         7.9
18Oct67                     8.0                      7.8                         7.9
 !Nov67                     7.5                      7.7                         8.0
15Nov67                     7.4                      7.8                         7.8
29Nov67                     7.7                      7.7                         7.7
13 Dec 67                     8.2                      7.7                         7.6
27 Dec 67                     6.9                      7.6                         7.8
10 Jan 68                     7.5                      7.4                         7.6
24 Jan 68                     7.9                      7.5                         7.6
 7 Feb 68                     7.6                      7.6                         7.6
20Feb68                     7.7                      7.2                         7.5
 5 Mar 68                                             7.5                         7.6
12 Mar 68                     8.4
27 Mar 68                     7.6                      7.6                         7.6
10 Apr 68                     7.7                      7.7                         7.7
24 Apr 68                     7.9                      7.5                         7.7
 8 May 68                     7.6                      7.8                         7.9
20 May 68                     8.2                      7.8                         7.9
 5 Jun 68                     8.7                      8.0                         8.0
19 Jun 68                     7.4                      8.0                         8.0
30Jul68                                             7.8                         7.9
27Aug68                                             7.6                         7.9
 2Oct68                                             8.4                         8.7
 6Nov68                                             7.7                         8.0
 9 Dec 68                                             7.6                         7.8
14 Jan 69                                             7.4                         7.5
27 Jan 69                                             7.4                         7.5
 9 Apr 69                                             7.3                         7.4
 2 May 69                                             7.6                         8.0
 5 Jun 69                                             7.5                         8 0

-------
                                                                           307
                                   TABLE 8


                         Solids Changes in Aerated Lagoons

                                           Solids mg/Hter

                       Raw                    Primary               Secondary

Date             TVS         VSS        TVS        VSS        TVS        VSS

15Nov65                                                        301         24
14 Dec 65                                  436        144        294         36
11 Jan 66          536          220         274        116        363         96
 1 Feb 66          676          316         376        148        346        104
 8 Feb 66          386          152         418        132        368         52
15 Mar 66                                  258         80        261         92
29 Mar 66                                  250         16        184          0
11 May 66                                  349         92        293         40
 6Jwi66                                  330         60        273          0
22Jun66          766          312         461        156        352        100
18 Jiil 66                                  582         92        530         84
10AUB66                                  528        216        588        160
2lSep66          450          136         396        124        400         60
 2 Nov 66          444          140         316        120        320         72
 7 Dec 66          688          224         450        112        295         30
11 Jan 67          470          184         392        172        332         80
 9 Mar 67          480          236         488        112        312         72
22 Mar 67          512          228         278         64        294         68
19 Apr 67          558          192         276         98        235         52
23Aug67          490          114         582        160        498         70
 6Sep67          388          122         474        104        446         46
20Sep67          460          200         462        100        486         46
 30ct67          406          184         420        116        348         36
180ct67          476          212         418        104        426         36
 1 Nov 67          438          164         332        124        346         48
15 Nov 67          590          220         312        100        278         20
29 Nov 67          496          144         268         92        292         24
i^TWfi?          590          204         468        160        o
-------
 308
                                    TABLE 9
                         Coliform Changes in Aerated Lagoons

                                             Coliform/100 ml
   Date

29 Mar 66
11 May 66
 6 Jun 66
22 Jun 66
21 Sep 66
 2 Nov 66
 7 Dec 66
11 Jan 67
 9 Mar 67
22 Mar 67
19 Apr 67
23 Aug67
 6 Sep 67
20 Sep 67
 3 Oct67
18 Oct 67
 1 Nov 67
15 Nov 67
29 Nov 67
13 Dec 67
27 Dec 67
10 Jan 68
24 Jan 68
 7 Feb 68
20 Feb 68
 5 Mar 68
12 Mar 68
27 Mar 68
10 Apr 68
24 Apr 68
 8 May 68
20 May 68
 5 Jun 68
19 Jun 68
30 Jul 68
27 Aug 68
 2 Oct 68
 6 Nov 68
 9 Dec 68
14 Jan 69
21 Feb 69
27 Mar 69
 9 Apr 69
 2 May 69
 5 Jun 69
  Raw
4x10*
5x10*
3x10*
2x10*
3x10?
5 x 10*
5 x 10*
5x10*
3x10*
1x10*
1x10*
1x10*
6 x 10*
5x10*
8x10*
3x10,
4x10*

1x10*
Ix
2 x 10,
8x10*

2x10*
3x10,
2x10*
9x10*
6x10*
1x10*
4x10*
3 x 10*
     *
3xl06
Primary

4X10*
2x10°
6x10*
8x10*
7x10*
8x10*
1x10*
1x10*
3 x 10*
4x10*
2x10*
2x10*
7x10*
7x10*
5x10*
6x10*
9 x 10*
ixio*
5 x 10*
6x10*
ixio*
8x10*
9x10*
9x10*
4x10*
8 x 10*

7x10*
8x10*
6x10*
7x10*
5x10*
9x10*
1 x 10*
6x10*
5x10*
4x10*
9x10*
1x10*
1 x 10*

6x10?
6 x 10*
3x10*
9xlOs
                                                Ix
                                                1 x
Secondary

  1x10*
  2x10*
  1x10!
  1x10*
  2x10*
  6x10*
  7x10*
      10*
      10*
  2x10*
  7x10*
  2x10*
  3x10*
  1x10*
  6x10*
  2x10*
  5x10*
  8x10*
  4x10*
  2x10*
  5x10*
  1x10*
  4x10*
  6x10*
  4x10*
  9x10*

  3x10*
  1x10*
  2x10*
  1x10*
  1x10*
  5x10*
  4x10*
  2x10*
  4x10*
  6x10*
  2x10*
  4 x 10?
  3x10*

  2x10*
  4 x 10*
  3x10*
  IxlO4

-------
                                                                        309
                                 TABLE 10

                     Fecal Coliform Changes in Aerated Lagoons

                                        Fecal Coliform/ 100 ml

  Date                   Raw                 Primary               Secondary

29 Mar 66                                      1 * «*                 4 x 10*
11 May 66                                      7 x 10s                 2 x 10
 6Jun66               '      _                7x10                  7x10

                        lxl°                 l^i                   x  :

                        8xio<                is1*                 n  :

                        23*$                 xl°o*                 111%
    r                   3xlO«                3xlO«                 2x10*
 9Mar67                2 x 10'                1x10*                 4x10
22 Mar 67                6 x 10s                1 x IjJ                 5x10
19 Apr 67                1x10^                3 x 10j                 1x10
23Aug67                Ixioj                4x10                  3x10
 6Sep67                IxlQj                2x10                  6x10
20Sep67                2xl0;                2x10                  4x10
 30ct67                3x10^                2x10                  3x10
180ct67                2x10^                4x10                  6x10

 lNov67                lxl°7                oX^                  fixlo4
15Nov67                3x10^                9x10                   6x10
29Nov67                5x10^                1x10                   9x10
13Dec67                2x10^                2x10                   6x10
27 Dec 67                 2 x 10 J                3x10                   2x10
10Jan68                 1 x loj                3x10                   2 x 10fi

                         ?-s                  "«:                       :
 12 Mar 68                 3 x 10                      6                  8 x 10s
 2?Mar68                 4 x 10*                J x 10                  « x JJ5
 10 Apr 68                 5x10^                | x 10,                  J « JJ,
 24 Apr 68                 7x10                 ^ x o.u                       s
  8May68                1 x 10j                2x10                  2 x 10g
 20 May 68                3 x ICT                3 « 10ft                  5 x 10,
  5Jun68                 4x10                 2 x 10ft                       s
 19Jun68                 1x10                 3 x 10fi                       4

 30 Jul 68                                       I x JJ6                  2 x 10s
 27Aug68                                      3xl05                  4xl04
  2 Oct 68                                       J J }J6                  5 x 104
  6Nov68                                      **{QS                  8X104
  9 Dec 68                                      Jx JJs                  5 x 104
 14 Jan 69                    , «                B X 1U
 2lFeb69                4x10                      5                  3 x 104
 27 Mar 69                                       *   s                  ! x io5
                                                 X
  9 Apr 69                                          QS                  2 x IO4
  2 May 69                                      2 x 10s                  1 x IO3
  5 Jun 69                                      2 X 1U

-------
 310
                                    TABLE 11

                        Enterococci Changes in Aerated Lagoons

                                            Enterococci/100 ml
   Date

11 Jan 66
  1 Feb 66
  8 Feb 66
15 Mar 66
29 Mar 66
11 May 66
  6 Jun66
22 Jun 66
18 Jul 66
10 Aug 66
21 Sep 66
  2 Nov 66
  7 Dec 66
11 Jan 67
  9 Mar 67
22 Mar 67
19 Apr 67
23 Aug 67
  6 Sep 67
20 Sep 67
  3Oct67
18 Oct 67
  1 Nov 67
15 Nov 67
29 Nov 67
13 Dec 67
27 Dec 67
10 Jan 68
24 Jan 68
  7 Feb 68
20 Feb 68
  5 Mar 68
12 Mar 68
27 Mar 68
10 Apr 68
24 Apr 68
  8 May 68
20 May 68
  5 Jun 68
19 Jun 68
30 Jul 68
27 Aug 68
  2 Oct 68
  6 Nov 68
  9 Dec 68
14 Jan 69
21 Feb 69
27 Mar 69
 9 Apr 69
 2 May 69
 5 Jun 69
 Raw

4 xlO4
2xl04
IxlO2
7xl04
8 xlO5
8xl05
8xl05
9xl05
2xl06
IxlO6
8xl05
7xlOs
9xlOs
6xlOs
3xl05
8xlOs
9xlOs
4xlOs
6xlOs
7xlOS
6xl05
5xl06
IxlO6
4 xlO5
8xl05
IxlO6

4xl05
2xlOs
2xlOs
8xlOs
4x10*
IxlO6
2xl05
2xl05
1x10°
Primary

IxlO4
4xl02
5xl02
IxlO5
8xl04
3xlOs
2xlOs
2xlOs
IxlO5
IxlO5
2xlOs
2xlOs
6xl05
4xl05
5xl05
4xlOs
2xlOs
4xl04
IxlO5
1x10
IxlO5
2xl05
2xlOs
2xl05
2xl05
7xl05
3xl05
2xl05
4xl05
4xlOs
3xl05
4xl05

2xlOs
2xl05
3xlOs
3xlOs
IxlO5
IxlO5
IxlO5
IxlO5
9xl04
IxlO4
5xl04
2 xlO4
4xl04

6xl04
5xl04
8xl04
3xl04
Secondary

  9xl03
  4 xlO2
  IxlO2

  3xl03
  IxlO4
  IxlO3
  IxlO2
  IxlO2
  IxlO2
  6xl02
  3xl03
  6xl03
  7xl04
  2xl05
  2xl05
  4xl04
  2 xlO3
  3 xlO3
  8xl02
  2xl03
  2 xlO3
  8xl03
  7 xlO3
  2 xlO4
  IxlO5
  6xl04
  9 xlO4
  IxlO5
  2xlOs
  2xl05
  2 xlO5

  1 x 10s
  8 xlO4
  7 xlO4
  4 xlO4
  IxlO4
  3 xlO3
  2 xlO3
  IxlO3
  2xl03
  IxlO3
  3xl03
  4 xlO3
  5xl03

  3xl03
  IxlO4
  2 xlO3

-------
                                                                            311
                                   TABLE 12

                      Total Bacterial Changes in Aerated Lagoons

                                             Bacteria/100 ml

  Date                    Raw                  Primary                 Secondary

llJanSG                 3x10*                 2x10*                   6x10*
 !Feb66                 7xl07                 1x10°                   5 x 10
 8Feb66                 4 x 107                 8 x HT                   1 x 10
15 Mar 66                                        8x10*                   7x10
29 Mar 66                 3 x 108                 3 x 10*                   8 x 10
11 May 66                                        4 x 10»                   5 x I0j
 6Jun66                       g                 9x10'                   2 x 10 J
22Jun66                 2 x 109                 1 x 109                   3x10
18 Jul 66                                        2 x 10*                   4 x 10*
10Aug66                       8                 2x10*,                   2x10
21Sep66                 9x10*                 1 x 1Q»                   9x10
 2Nov66                 9x10*                 4 x 109                   3x10
 7 Dec 66                 5 x 108                 6 x 10°                   2 x 10
11 Jan 67                 4x10*                 3x10*                   3x10
 9Mar67                 3 x loj                 2 x 10*                   3x10

                         -IS          '       ?:X:                     x  *
20    67                  3x10^                 9x10                    7x10
      67                  3x10                  2x10*                    2x10
                                                      *
180ct67                  2xi09                 5x10*                   3x10
 !Nov67                  2xl09                 1x10                    2x10
15Nov67                  SxlO9,                 7x10                    3x10
29Nov67                  2xl09                 3x10                    2x10
13Dec67                  1 x 109                 2 x 10*                   1 x 10g
27Dec67                  9xl09                 4x10                    4x10
10 Jan 68                  2 x 109                 3 x 108                   2x10*

^FebeS                  3xl09                 3xl09                   2x10*
20Feb68                  2 x 109                 3x10                    2x10
                                                                           x
27Mar68                 2 x lo                  2x1                      x
10 Apr 68                 2x10^                 3x10                    2x10

24APr68                 2xl°9                 iXJS«                   6xio8
  8 May 68                 2x10^                 4x10                    6x10
20 May 68                 2 x 10*                 1x10                    1x10
  5 Jun68                 Gxioj                 1x10                    5xlO?
19Jun68                 4xl09                 2x10                    8x10
qn Tlli CQ                                         1 x 10n                   d x 1U7
??A^f«                                        6xl09                   9x10^
27 Aug 68                                             9                   4x10*
                                                 4x10                    *xiu
                                                                               8

  6Nov68                                             9                        7
       69                       8
 21Feb69                 2x10                       .                   2x10*
 27Mar69                                        4x10                    2 x 108
  9Apr69                                        3xl09                   2 x 10g


-------
               DISINFECTION AND TEMPERATURE  INFLUENCES


                               Cecil Chambers and Gerald Berg

                                      INTRODUCTION

 The purpose of this discussion is to explore a number of disinfection methods, some conventional,
 and some not  so conventional, and to  examine their  potential strengths  and weaknesses for
 disinfecting effluents under cold climate conditions. A second objective will be to outline the need
 for research to  assist in developing guidelines for the most efficient practical use of disinfectants
 where extremely low temperatures prevail.

 Disinfection, like primary settling,  aeration,  and  other steps  in waste  treatment, cannot be
 considered independently  of other phases of the process. All of these factors affect the quality of
 the final effluent produced. This is especially important in  the situation we are concerned with,
 because the arctic environment influences the various methods of waste treatment in ways which
 have profound effects on disinfection efficiency.

 In general, effluents in arctic areas are relatively crude. A majority of  the treatment plants in
 Alaska have only primary  settling. The high turbidity and organic content of such effluents make
 them  difficult  to disinfect by any method available. In addition, because  biological oxidation
 proceeds at a slow pace at low temperatures, the effluents from secondary  activated sludge plants
 and other biological treatment processes are  incompletely oxidized and high in ammonia nitrogen
 content.

 Because its primary purpose is the prevention of transmission of disease, disinfection is considered
 the most  critical step in waste treatment. Nevertheless, application of massive doses of chlorine,
 for example,  should  not be  accepted  as  a  substitute for  adequate  removal  of  solids  and
 stabilization of  soluble organic matter.  When  such crude  effluents are discharged to receiving
 waters,  the  low  biological activity at arctic temperatures  will contribute to an  increasing and
 cumulative load of oxidizable material, especially in lakes, streams, and estuarine waters.

 Dissolved  oxygen levels frequently reach  extremely low concentrations under ice cover in Alaska.
 Under  these  circumstances,  any  attempt to  circumvent adequate treatment  by  excessive
 application of  disinfectants will  further deplete the critically low dissolved oxygen supply. In
 addition, the question is being asked with increasing frequency, are we, in applying massive doses
 of chlorine to crude effluents, creating toxic chlorine addition  products that adversely affect the
 flora and fauna in the receiving water? What is the effect on the aerobic food chain? When such
 possible toxicity  is superimposed  on the effect of an already precariously low oxygen level, it may
 lead to the demise of a critical segment of the food chain. This can be especially important in cold
 climate  areas where biological productivity of waters is low. The consideration of non-residual
 disinfectants may have  potential  to  resolve  or minimize this problem in  some low temperature
 situations. Another approach is neutralization of the disinfectant before discharge or selection of a
 chemical disinfectant that  is effective at minimum residual levels.

The efficiency of chemical disinfectants decreases with decreasing  temperature {Clarke and Chang,
1959). Another  problem  that should be considered is  the extended survival  of  organisms at

                                            312

-------
                                                                                      313


near-freezing  water temperatures. Both  enteropathogenic and  coliform  bacteria are  known to
survive in water for extended periods of time at very low temperatures, and viruses survive for long
periods when frozen in ice. Clark (1970) has pointed  out that in Alaska, "Stream and lake waters
will be used for drinking water for some time to come without treatment in spite of all efforts to
provide, require, and encourage treatment."

Because of prolonged survival of pathogenic organisms in cold water and ice, the organisms may be
transported by currents under the ice and by drifting ice when break-up time comes to serve as
sources  of  infection far from  their point of origin. In addition, there is widespread  groundwater
contamination  in  many areas especially during  spring thaws. This  is further aggravated by
inadequate disinfection of wastes and extended  survival of contaminants at low  groundwater
temperatures which are frequently just above the freezing point. These  conditions combined with
the widespread  practice of drinking  untreated  water emphasize the importance  of  thorough
disinfection of effluents in cold climate areas.

                   GENERAL AND BACTERICIDAL CONSIDERATIONS

Chlorine

Chlorine is more widely used  for disinfection of water and wastewater than  any other chemical
agent. Regardless  of  whether chlorine is added to water as liquid  chlorine  (CI2), sodium
hypochlorite (NaOCI), or calcium hypochlorite {Ca(OCI)2}, the same disinfecting entities will be
produced  (Fair et al., 1948). In  wastewater disinfection, two  forms of chlorine are of primary
interest: they are  (1) hypochlorous acid (HOCI) and (2) chloramines.

A third form, hypochlorite ion  (OCI~), has little if  any disinfecting efficiency. The  hydrolysis
product of the reaction of chlorine and water, HOCI, is the predominant form in which chlorine
exists in aqueous solution between pH levels of  2.0 and  7.0. Between pH 7.0 and 8.0 progressive
ionization  of the HOCI takes  place. At the higher pH level most of the  chlorine exist as OCI' ions.

Significant amounts of ammonia-nitrogen, probably 20 ppm or more, can be  anticipated in arctic
effluents.   This  ammonia   will  combine  with   chlorine   to  produce  chloramines   of  which
monochloramine  is the dominant, and probably the mostgermicidal, form of chlorine that will be
present at the pH of  most effluents  (Baker,  1959). The exception would be break-point
chlorination,  where  ammonia-nitrogen  is  destroyed  by  application  of  chlorine   at  a
chlorine-to-nitrogen ratio of approximately 9 to  1 (Butterfield,  1948a) to provide residual HOCI.
Chlorine demand, caused by organic components of sewage, is a serious problem in disinfection of
wastewater. Assuming no chlorine demand, approximately 180 ppm of titratable chlorine would
be required to  reach the  breakpoint and provide  residual HOCI at  an ammonia-nitrogen
concentration of 20 ppm.  Except initially, HOCI is not likely  to be present  in most chlorinated
effluents.

Monochloramine is a relatively  inefficient disinfectant when  compared to HOCI (Butterfield,
 1948b). Butterfield and Wattie (1946) in tests with chloramine* using Escherichia coli, Salmonella


*While the term chloramine is used in their report, conditions were such that monochloramine was
the dominant form produced.

-------
 314
 typhosa.  and Shigella sonnet as test organisms,  concluded that,  "A reduction of  20° C  in
 temperature (20° C - 25° C to 2° C - 6° C) requires 9 times the exposure period, or 2.5 times as
 much chloramine to produce a 100% kill." Decreasing the hydrogen ion concentration decreases
 the disinfecting efficiency of both HOC! and monochloramine.

 When the effects of an unfavorable temperature and pH are combined, the disinfecting efficiency
 of monochloramine is very  seriously  depressed;  these effects are  demonstrated by Butterfield's
 (1948fa) data which are presented in  Figure 1. The advantages of maintaining the lowest possible
 pH,  consistent with  avoiding  corrosion problems, are readily apparent when using HOC!  or
 monochloramine as a disinfectant at low temperature.

 Iodine

 At acid pH levels, iodine exists primarily in  the elemental state and forms tri-odide and higher
 iodides in the presence of increasing  quantities of iodide ions. At increasing pH levels, elemental
 iodine hydrolyzes to hypoiodous acid (HOI) which, in the absence of excessive iodide ions, may
 constitute about  40% of the iodine  at pH 8.0. As the pH increases beyond this  level, the HOI
 decomposes to iodates which  are essentially non-germicidal. Elemental iodine and several of  its
 derivatives are efficient disinfectants, although not quite as efficient as HOCI. While iodine is more
 expensive than chlorine, it does not form iodamines and has relatively low reactivity to organic
 matter (Chang, 1966). Accordingly, iodine has considerable potential for circumventing some  of
 the problems encountered with chlorine.
                           CO
                           Ul
                           a:
                                                     AFREE (HJDWNE
                                                        at 20iwn   -
                              aoe
                                               9    10    II
                                                pH
                                      100% KILL OF ESCHERICHIA COL1
FIGURE 1  The combined  effort of  variations  in  pH  and temperature on the  disinfecting
            efficiency of free chlorine and chloramine. After Butterfield (1948b)

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                                                                                         315
                                        P-6   Sityphl-murium
                                        C-36 E. coll
                                        P-9   S sonnel
 FIGURE 2  Average ppm iodine required to kill all test bacteria in 1 minute. After Chambers et
             al. (1952)
 Chambers et al. (1952) in tests with E. coli, Aerobacter aerogenes. Streptococcus fecdis, and three
 species of Salmonellae, including S. typhosa, and four species of Shigellae, concluded that, "At a
 given exposure time and pH the iodine concentration required to kill at 2° C to 5° C may be as
 much  as four times greater  than at 20°  C to 26°  C," and ". .  . increases in pH  reduce  the
 bactericidal action of iodine." These effects are illustrated in Figure 2 which presents the results
 obtained with a  pollution index  organism, E. coli, and the  two most resistant enteropathogenic
 bacteria tested, Salmonella  typhimurium and S. sonnet.  Recent information indicates that  the
 most desirable pH range for disinfection with iodine is pH 7.0 to 8.0 (Berg, 1970).

 Because iodine has not been widely used for disinfection of water and wastewater, methods of
 application are  not as universally understood  as is the  case with  chlorine.  Chang  (1966)  has
 designed a system for application of  iodine to water that can be adapted easily to disinfection of
 effluents. His report also presents an excellent bibliography on disinfection of water with iodine.
 In addition, a patent has been granted on a system designed to convert iodine to the gaseous state
 for use in disinfection of water (Starbuck, 1967).*

 Excess Lime

 In water and  wastewater  treatment,  lime is usually considered primarily as a flocculating agent.
While there are some  problems such as sludge disposal  associated with the use  of lime, lime
flocculation can markedly reduce  the solids content of raw sewage and the overall BOD reduction
may be as much as 70% (Bishop and Sanoworth,  1970).
*References to commercial products are not to be construed as endorsement by the Federal Water
Quality Administration.

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316

Flocculation with lime  can  remove or destroy a relatively high percentage of the microorganisms
present. What is not generally realized  is that lime can also be used as a disinfectant if pH and
contact time are maintained at suitable levels, and it is not subject to the organic demand problems
of halogen disinfectants and ozone. The data of Wattie and Chambers (1942), presented in Figure
3 show the disinfecting efficiency of increasingly high pH at temperatures of 0° C to 1° C and 20°
C to 25° C with E. coli.

Results obtained by the same people in comparable tests with S. typhosa are presented in Figure 4.
Riehl  et  al. (1952) augmented  this work  in subsequent  studies  with a  wider spectrum  of
pathogenic  organisms at several temperatures ranging  from  2° C  to  25°  C.  Their results are
comparable to those presented in Figures 3 and 4.

Ozone

Although ozone is widely used as a disinfectant throughout Europe, its primary use for treating
drinking water  in the United States is for the removal of taste, odor, and color.

There  is very little  information  in  the  literature relating to the possibility  of  using ozone as a
disinfectant for waste treatment plant effluents. Stumm (1958), however, stated ". . . ozone has to
be  considered as a  potential  disinfectant for water and sewage." He also indicated the need for
research in  his concluding statement  ".  .   . more investigations  are needed  to evaluate the
applicability of ozone  as a practical tool for  the sanitary engineer in water  treatment and waste
disposal."  Recently  Smith  (1967)  presented data obtained  in  studies with effluent from  a
municipal activated sludge plant. Tests were run with non-nitrified effluent, nitrified effluent, raw
g
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                                  23456789

                                           TIME IN HOURS
                                                                     10
 FIGURE 3  Death rate of Escherichia coli at various pH ranges at 0° - 1.0° and 20° - 25° C. After
             Wattie and Chambers (1942)

-------
                                                                                       317
100

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                                           TIME IN HOURS


FIGURE 4  Death rate of Salmonella typhosa at various pH ranges at 0°  - 1° and 20° - 25°  C.
            After Wattie and Chambers (1942)
sewage  filtered  through glass  wool, and  raw  sewage (aluminum  sulfate  precipitated).  They
concluded that disinfection at  the 99% kill level was not  attained with secondary effluents, and
results with  raw sewage were less acceptable. In subsequent laboratory pilot scale studies they
concluded that ". .  . an ozone dose of 7 to 10 ppm may be sufficient for disinfection of municipal
sewage treatment plant effluent under these circumstances."

In considering the possible  applicability of  ozone for disinfection of wastes under cold climate
conditions, the fact that ozone is a very powerful oxidizing agent makes it susceptible to organic
demand. This  characteristic is offset to a degree by the fact that some reduction in BOD occurs
and the end products of the oxidation are non-toxic. In addition, ozone is rapidly dissipated and
no toxic residual disinfectant remains in the effluent. A distinct advantage is the fact that ozone is
not susceptible to reductions in efficiency in the presence of ammonia, as is the case with chlorine.
Increased solubility  at the low temperatures encountered in the Arctic  may also be an advantage.
However, the excessively high iron content of some Alaskan groundwaters (6 to 14 mg/l common;
Clark, 1970) may be a problem if the iron is in  the reduced state and such waters find their way
into the disposal system.

Bromine

Bromine is recognized as a powerful bactericidal  agent. Although it is somewhat more expensive
than chlorine, bromine has been used with considerable success as a swimming pool disinfectant in
Illinois  (Klassen and Sieg,  1948). Nevertheless,  until recently,  little  attention has been  given to
investigation of  bromine for use in disinfection of water and even less  consideration has been given
to the potential of  bromine for disinfection of wastewater. The work of Johannesson (1960) has

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 318

provided a basis for a better understanding of the fundamental behavior of bromine as a water
disinfectant,  and  this  has  served as  a  stimulus to increased  interest in  bromine. Because
bromamines are essentially as germicidal as free  bromine, a highly potent disinfectant, bromine
may have potential for use  in disinfection of waste treatment plant effluents especially in cold
climate  areas where effluents with high ammonia content may be expected to be a continuing
problem. Bromine has the disadvantage, however, of being relatively susceptible to organic demand
and elevated pH (9.0-9.5) is necessary to produce significant amounts of bromamines.

The  Federal Water Quality Administration has been sponsoring research to determine the relative
efficiency of chlorine and bromine for disinfection of activated sludge plant effluent (Solloetal.,
1970). In this work, both dosage and residuals  of  chlorine and bromine are being correlated with
percent survival of coliforms, fecal coliforms, and total bacterial numbers. Anomalous results have
been obtained with chlorine at 30° C (pH 9.0)  and these  results cannot be explained. Control of
bromine concentrations  has  proven  difficult  because   of  the  rapid  bromine  decay  rate.
Combinations  of chlorine  and bromine are  also being evaluated, and it appears that pretreatment
with chlorine,  followed  by bromine,  may  produce effective disinfection at a  lower  cost than
bromine alone. The preliminary results obtained indicate that ". . . the efficiency of disinfection is
almost independent of the chlorine dosage, so long as it  is greater than the immediate demand.
Thus, the function of the clorine appears  to be  only that of conserving bromine by satisfying
demand." The minimum  test temperatures in  this project were  10° C, but this  work is being
continued and tests at 0° C to 2° C are planned for  the future.

Pasteurization

Pasteurization, because it  is unaffected by the chemical quality of wastes, may be feasible in arctic
climates in some locations. Sludges and effluents from sanitoria have been disinfected with heat in
a number of  European countries and  sewage  sludge  has been pasteurized before  spraying on
agricultural  land  in  Germany  (Kugel,  1968). Goldstein et al. (1960)  tested  a system  for
pasteurization of water that was effective in destroying coliform organisms.  They considered  the
principal advantages to be  reliability  and  simplicity,  both important factors in  Alaska. On a
household scale, costs were  estimated  to  be approximately  $1.00 per 1,000 gallons, but they
would have  been lower if the unit had been operated constantly. At cold climate temperatures,
costs would be somewhat higher  and revised design criteria  would  probably be necessary with
wastewater to  minimize fouling of heat exchangers. Construction plans for this unit have been
published (U.S. Public Health Service, 1959). Seiberling and Harper (1955) have also reported on a
pasteurizer design  for successful  high temperature short time exposure of  water.  Harper stated
(personal communication to  C.  W.  Chambers,  1965) that  after  approximately 10  years of
operation ". .. this unit has been extremely  satisfactory..."

Miscellaneous Disinfectants

Gamma radiation has been advocated by some people for disinfection of wastes. The fact that it is
a physical process  might indicate potential  for low temperature use, but there appears to be little
in the work reported to offer encouragement. There have been  reports of  a marked synergistic
action of gamma radiation on the disinfecting action of chlorine, and this could be advantageous
under cold climate conditions; however, the work reported has been inadequately con trolled. The
authors are investigating this phenomenon and  results to date show no evidence of any practically
significant synergistic effect with monochloramine when conditions are adequately controlled.

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                                                                                         319
Ultraviolet light  has some potential  for  disinfection  of high quality  effluents.  The types  of
effluents produced in Alaska may be high  in iron and color content; and both of these interfere
seriously with the  disinfecting efficiency of ultraviolet  light. Another trait  that has to  be
considered is the fact that low ambient temperatures reduce lamp efficiency. It is possible that
ultraviolet light may have some potential for use with effluents that have been highly clarified by
chemical coagulation, provided interference from  color and residual lime floe are not encountered.
                 o
                 o
                    .1
                  .0*
                  .08
                  .07
                  .06
                  .09
                I  I  I  I  I
A .6 .7JB.»I
2     3   4
MINUTES
                                                      667S9IO
            FIGURE 5   Inactivation of poliovirus 1 by HOCI. After Weidenkopf (1958)
                              VIRUCIDAL CONSIDERATIONS
Chlorine

Hypochlorous acid (HOCI) is a rapid virucide (Fig. 5) (Weidenkopf, 1958), while the OCI" ion is a
poor virucide, if  in fact it  kills  any viruses  at  all.  In  a clear aqueous solution, even  at low
temperature, chlorine is a very rapid virucide at acid pH, and a very slow virucide beyond mildly
alkaline pH levels. Chloramines are slow virucides (Fig.  6)  (Shuval, 1966), usually too slow for
effective  treatment  of virus-bearing  water.  Even  the  quick virucidal  activity  that  occurs
immediately after chlorine is added to  a  sewage  effluent, an activity that reflects  the action of
HOCI  before it has all  reacted  to form chloramines,  leaves a large  amount of  virus  to  the
slow-killing chloramines.  Since even  very small  numbers of viruses are capable of producing
infections (Plotkin and Katz, 1967), it is clearly important that all viruses should be removed from

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 320

any waters with which man may come in contact. Thus, when HOCI cannot be maintained, or
when its presence cannot be tolerated, we must consider other disinfectants.

Survival of Viruses in Sewage and Water

Freezing brings about the formation of ice crystals in bacteria, and with this, eventual disruption
of the cellular membrane of many cells. The result is a gradual to rapid die-off of bacteria, the rate
depending on the species, temperature, and other environmental factors. Viruses are not cellular,
and  freezing does not destroy them. To the contrary,  freezing is the best known method for
storing viruses, and the lower the temperature, the better. In the laboratory viruses are preserved
by cold-temperature storage. Viruses may be stored at -70°  C for a decade or more. Thus, in the
cold environment of  the  North, the  normal die-off of  viruses experienced in warmer climates
probably does not occur.

Figure 7 (Berg, 1966) shows the relationship between temperature and time for the destruction  of
99.9% of three different viruses in stored sewage. This graph was prepared from data obtained by
others (Clarke, Berg et al., 1962). At  10° C, 99.9% destruction of echovirus 7 took more than 100
days, and  both  polivirus 1 and echovirus  12  required more than 60 days. Thus, enteroviruses can
survive in  sewage for many months at low  temperatures. In ice, survival time will exceed cold
water survivals and, of course, the lower the temperature,  the longer will be the survival.
                                  8.5mg/l residual (combined) chlorine
                                           -II mg/l  applied chlorine
                                                	Shuval *t al (1966)

                                                ____Lothrup and Sproul
                                                                     (1969)
                                           3       4
                                            HOURS
                  FIGURE 6  Inactivation of poliovirus 1 by applied chlorine

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                                                                                           321
                                  ECHOVIRUS 12
                                  ECHOVIRUS 7
                                  POLIOVIRUS I
                                                     20
                                            TEMPERATURE  'C

  FIGURE 7  Relationship between time  and temperature for 99.9% reduction of virus in stored
              sewage. After Clarke, et al. (1962) as revised by Berg (1966)

 Viruses do not survive as long in river water as they do in sewage (Clarke, Berg et al., 1962; Berg
 and German, 1970) and there is some evidence that they do better in lightly polluted water than in
 heavily polluted water (Clarke. Berg et al.,  1962). Their survival in distilled water is also of long
 duration.

 There is no simple explanation for survival patterns of viruses in waters of various qualities. Since
 autoclaving  increases survival in certain river  waters, microbial life, their enzymes or other
 heat-labile matter may account  for some of the pattern. Certain  divalent cations are known to
 increase the survival of some  viruses, and decrease it for  others.  Clearly, the chemistry  of  the
 water, as well as the temperature, is an important determinant of virus survival.

 Iodine

 Elemental iodine is a rapid virucide, but not as rapid as HOCI. Elemental iodine, however, can be
effective in  circumstances that impede the effectiveness of HOCI. In the presence of ammonia, for
example,  where HOCI reacts to form the relatively slow chloramines, the iodine remains free to
react with viruses. Elemental iodine is a faster virucide than  chloramine (Berg and Berman, 1970).

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 322
                       349 678910
  20  30 401

MINUTES
       FIGURE 8   Inactivation of coxsakievirus A9 by elemental iodine. After Berg (1964)

At pH 8.0, where most  HOC) has ionized to the poorly virucidal OCI" ion, much of the elemental
iodine has hydrolyzed to HOI which is  considerably more virucidal than  the elemental iodine
(Berg, unpublished data).

Figure 8  shows the  relationship  between  time and elemental iodine concentration  for the
destruction of 99% of coxsackievirus A9  over a three  temperature range (Berg, Chang and Harris,
1964). Four other viruses tested under identical conditions were only slightly less resistant. E. coli,
Pseudomonas  aeruginosa,  Alcaligenes fecalis and Staphylococcus  aureus  were  about  equally
sensitive to elemental iodine, and depending upon temperature, about 1,100 to 1,700 times more
sensitive than  coxsackievirus A9 (Berg, unpublished  data). The  QIC for coxsackievirus  A9 was
about 4.5, but it was apparently less for E. coli.

From Figure 8, it is possible to determine both the times for 99% destruction of the virus over a
continuous temperature range at constant I? concentrations, or alternately, I2 concentrations for
99% destruction of the virus over a continuous temperature range at constant times (Berg, 1970).

Ozone

Despite its long widespread use in  Europe, there are relatively few data  available  on the virucidal
efficiency of ozone.

Figure 9,  however, gives an approximation of what ozone can achieve. Poliovirus 1 was inactivated
at a  rapid rate in river water with only a few tenths of a mg/l of ozone, apparently at about 25° C

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                                                                                      323
(Coin,  Hannoun and Gomella, 1964). Poliovirus 2 and 3 were inactivated  more quickly under
similar circumstances (Coin, Gamella et al., 1967).
                    10,000 -
                  o
                  n
                                                               16
IB
                               7     10     13

                              MINUTES

FIGURE 9   Inactivation of poliovirus 1 by ozone. After Coin, et al. (1964)
Ultraviolet Light

Ultraviolet light (UV), at a wavelength of about 250-260 m/a, is strongly bactericidal. Only limited
data exist, however, on the virucidal  capability of UV light. In distilled water at intensities of
4,000-11,000 Mw-seconds per cm. Huff et al. (1965) inactivated at least 99% of polioviruses 1,2
and 3, coxsackievirus A9, and echovirus 7. Only at  lower dosages did  small amounts of viruses
survive. In the presence of 9 standard units  of color, the UV  was slightly less efficient. Hill,
Hamblet and  Banton  (1969) evaluated  UV,  presumedly in  the 250-260  mn range, exposing
poliovirus 1  in seawater to 83/iw/cm2 of radiation 14 cm from the source. Although the dosage is
not completely clear, the rapid virucidal effect of the UV is evident (Fig. 10).

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 324
Gamma Radiation

Gamma radiation rapidly  destroys  viruses.  In a  menstruum  containing  salts  and serum 0.5
megarads  destroyed  90% of poliovirus 3. In distilled  water, where quenching  of  free radicals
produced  by the  radiation did not occur, 90% of  the virus  was destroyed by less than 0.11
megarads  (Sullivan, 1970).  Many other viruses tested fell into generally similar resistance patterns.
There is  little reason to anticipate, however,  that economically feasible methods of disinfecting
wastewater with gamma radiation will be developed.
                     .01
                                     10      19      20     28     30
                                       UV EXPOSURE (second*)
SO
         FIGURE 10 Incativation of poliovirus 1 with UV light. After Hill, et al. (1969)

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                                                                                         325
                                   RESEARCH NEEDED
Lotspeich (1969) states, "Design criteria are simply not available - and  this includes Scandinavia
and Soviet Russia as well as Alaska - to build  disposal systems that will function with assurance
under  the severe climatic conditions  of  northern  latitudes." To  those  of us  interested in
disinfection,  this indicates that research to solve the  problem of effective removal of solids and
soluble  organic  material should  have  a very high  priority if adequate  disinfection by  chemical
methods is to become a practical reality under cold climate conditions.

Information  should  also  be secured to provide satisfactory  answers to questions regarding the
survival of bacteria and viruses under natural conditions in water and bottom sediments under ice.
This information is badly needed to determine the effect of an influx of crude and inadequately
disinfected wastes on survival patterns under ice cover. Comparable studies of the same receiving
waters are needed  during open  water  periods to determine the effect of some of  the  violent
seasonal variations that occur in the Arctic.

It is also well recognized that a significant die-off of coliform and pathogenic bacteria occurs in ice
while viruses survive for relatively long periods. What, however, is the  effect on these survival
relationships  when incompletely disinfected effluents are frozen, especially when contact time has
been inadequate and some residual disinfectant remains? Research is needed to provide answers to
these questions.

The  disinfecting potential of lime should be  thoroughly investigated. It  may  be  possible to
combine successfully  the  use of lime as a disinfectant with  its ability to  physically remove
microorganisms  and a  high percentage  of solids and  oxidizable material. Such research  should
begin in the  laboratory, using raw and/or settled primary sewage at very low temperatures. The
effect  of increasing  pH  should be  related to the  holding time required  to  yield adequate
disinfection under the respective test conditions.

Bench-scale pilot plant studies with lime, or other disinfectants considered subsequently, should be
initiated just  as quickly as the  preliminary research provides adequate guidelines.

Iodine should be investigated  in parallel laboratory tests  with chlorine  using different types of
effluents. The inefficient disinfecting properties of chloramines, especially with viruses, combined
with the high chlorine demand of many effluents are  recognized. These factors create a need for
heavy chlorine dosage if adequate disinfection  is to be accomplished.  The organic demand effects
of effluents on iodine are not known. Work is  needed to evaluate these effects of effluents on the
disinfecting efficiency of iodine.  The research outlined should provide a basis for establishing the
true comparative efficiency of iodine and chlorine for low temperature disinfection of wastewater.

Preliminary  research  on the  use  of  ozone should  be considered to determine  whether ozone
demands, especially of the types of effluents to be treated in Alaska, would preclude its use. Some
guidelines regarding  research with  ozone for disinfection  of  individual  household wastes (toilet
wastes only) may be  available from Smith (1967) who mentions successful  treatment of such
wastes over a six-month period.

It should be  emphasized that  disinfection research should get out of the laboratory and into the
field for practical evaluation just as quickly as possible. The author is aware of the limited research

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326

resources available in most cold climate areas. Nevertheless, wherever possible, it seems desirable to
have the laboratory research most closely related to practical application done in the general area
where the field evaluation will  be made. In this way, personnel most familiar with the technical
problems encountered in the  laboratory and bench-scale pilot application studies will be available
for consultation and assistance in expediting field use.

In conclusion, I should like to point out that all disinfectant research should be planned to provide
the  best possible basis for determining overall costs for application  in  various locations. In Alaska,
for example, the cost of shipping lime would probably be prohibitive in some  inland locations, and
ozone  would  require electrical  service. We need  to develop a research  program  to  provide a
spectrum of proven disinfection processes from which a sanitary engineer can select the one most
applicable to a specific waste  disinfection problem. Only through such an approach will we be able
to satisfy the wastewater disinfection needs of Alaska and similar cold  climate areas.

                                       REFERENCES

 Baker,  R. J. (1959) Types and significance  of chlorine  residuals, J. Amer. Water Works Assn.,
     51:1185-1190.

 Berg, G. (1966) Virus transmission by the water vehicle. Health Lab. Sci., 3:90-100.

 Berg, G. (1970) Virus inactivation and removal, Presented at the National Specialty Conference on
     Disinfection, University of Massachusetts, Amherst, Massachusetts.

 Berg, G. and Berman, D. (1970) Unpublished  data.

 Berg, G., Chang, S. L. and  Harris, E. K. (1964)  Devitalization of microorganisms by iodine, 1.
     Dynamics of the Devitalization of Enteroviruses by Elemental Iodine, Virology, 22:469481.

 Bishop, D.  F. and Sanoworth,  R. B. (1970) Monthly Report FWQA  Contract No. 14-12-818 with
     the  District  of Columbia, Dept.  of San.   Engineering,  Available  from  Advanced  Waste
     Treatment Research Laboratory, FWQA, U.S. Department of the Interior, Cincinnati, Ohio.

 Butterfield, C. T. (1948a) Bactericidal properties of free and combined available chlorine, J. Amer.
     Water Works Assn., 40:1305-1312.

 Butterfield, C. T.  (1948b) Bactericidal properties of chloramines and free chlorine in water. Pub.
     Health Rept. (U.S.) 63:934-940.

 Butterfield, C.  T.  and  Wattie, E. (1946) Influence of pH and  temperature on the  survival  of
     conforms and enteric pathogens in water, Pub. Health  Rept. (U.S.) 61:157-192.

 Chambers,  C. W.,  Kabler, P. W.,  Malaney, G. R. and Bryant, A. (1952) Iodine as a bactericide,
     Soap and San. Chem., 28:149-165.

 Chang, S. L.  and del Aqua,  Yodacion (1966) lodination of water, Boletin de la Oficina Sanitaria
     Panamericana, 4:317-331. (Mimeograph, English, available from Dr. S. L. Chang, U.S. Public
     Health Service, Bureau of Water Hygiene, Cincinnati, Ohio.)

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                                                                                        327

  Clark, S. E. (1970) Personal communication, Alaska Water Laboratory, Fairbanks. Alaska.

  Clarke, N.  A.  and Chang, S. L. (1959) Enteric viruses in water, J. Amer. Water Works Assn
      51:1299-1317.

  Clarke, N. A.,  Berg. G., Kabler. P. W. and Chang, S. L. (1964) Human enteric viruses in water:
      source, survival and removability, International Conference on Water Pollution  Research
      London (1962), Pergamon Press, New York, N. Y. (523-542).

  Coin,  L, Hamnoun, C.  and Cornelia,  C. (1964)  Inactivation  by ozone of poliomyelitis  virus
      present in  water, La Presse Medicale, 72:2153-2155.

  Coin,  L., Gomelta,  C.,  Hamnoun, C.  and Trimoreau, J-C  (1967) Inactivation by  ozone of
      poliomyelitis virus  present   in   water   (Further   contribution).  La  Presse   Medicale
      75:1883-1884.

  Fair, G. M., Morris, J. C., Chang, S. L., Weil. I. and Burden, R. P. (1948) The behavior of chlorine
      as a water disinfectant, J. Amer Water Works Assn., 40:1051-1061.

 Goldstein, M., McCabe, L. J., Jr. and Woodward, R.  L. (1960) Continuous-flow water pasteurizer
     for small supplies, J. Amer. Water Works Assn., 52:247-254.

 Harper, W. J. (1965) Personal communication,  Ohio State Univ., Department of Dairy Technol.,
     Columbus, Ohio.

 Hill, W. F., Jr.,  Hamblet, F. E. and Benton, W. H. (1969) Inactivation of poliovirus type 1 by the
     Kelly-Purdy ultraviolet seawater treatment unit, Appl. Microbiol., 17:1-6.

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 Johannesson, J.  K.  (1960)  The  bromination of  swimming  pools.  Am.  J.  Pub.  Health,
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 Klassen, C. W. and  Sieg, J. G.  (1948) Swimming pool operations. State of Illinois Department of
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 Kugel, G. (1968) Jahresbericht of the Niersverband  Gruppenklaranlage, Viersen  (near Cologne,
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    Publishers, New York.

Riehl, M. L.,  Weiser, H. H. and Rheins, B. T. (1952) Effect of lime-treated water upon survival of
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Seiberling, D. A. and Harper, W. J. (1955) HTST pasteurization for the control of psychrophilic
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     5:56-67.

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        CRITICAL  REVIEW OF PAPERS  ON  TREATMENT PROCESSES
                                      Karl Wuhrmann
 Reviewing eight contributions of excellent and distinguished speakers is a delicate task considering
 the fact that the most pertinent paper has not been presented at this symposium. I mean the basic
 text, setting the specific goals and defining the special needs for water pollution control measures
 in countries with arctic climates. Like in any other geographic region waste treatment has to meet
 the requirements set by  the quality standards which are or have to be imposed  on the receiving
 water bodies by legislation or on the grounds of ecological exigencies. As anywhere, the quality
 standards of treatment plant effluents must be tailored to the local conditions in rivers and lakes,
 and the technology of treatment can only be decided upon when these conditions are known.
 Since this  basic concept was lacking, the  papers under review  necessarily  pointed in various
 directions, according to the personal association of each author to the keyword of "cold climate."

 Concerning the first fundamental question, namely "what has to be done?" three objectives have
 been  considered, i.e., the  conventional  problem of removal of  organics,  the abatement of
 eutrophicating effects of wastes and the health  hazards involved with sewage. No priorities have
 been set. AH of these  objectives might be important, however, at one place or another, and it was
 justified, therefore, to cover the respective technology to a certain extent.

 As to the second fundamental question "how can it be done?" the authors have mostly elaborated
 on the problem of  low temperature effects on process efficiency and design. Process efficiency is
 undoubtedly an important item in the present context. I should say, however, that it has much less
 weight in  practical water pollution  control than  such banal items as  sludge disposal or purely
 mechanical problems of operating machinery in an arctic  winter.  As a microbiologist I am not
 competent  to deal with  such technical matters.  Having some experience, however, with small
 treatment plants in the Alps up to altitudes of more than 9,000 ft., I wish  to indicate that these
 technical problems are by  far  dominating  every  other question which might arise  due to low
 temperature!

 In the group of papers reviewed by Dr.  Krenkel it has  clearly been  shown  that the  above
 mentioned objectives one and three, i.e. removal of organics and reduction  of health hazards, are
 most imperative in  the majority of Alaskan situations. It was made clear  also  that, besides  a very
 few large agglomerations where conventional  planning of plants may be adequate, mostly small
 population  centers exist, requiring the  utmost  technical  and operational  simplicity for  any
 treatment installation.

 I take the liberty to comment on the papers under the two headings:

 • Basic considerations as to biological processes at low temperatures, and

- Practical observations and experiences with treatment processes.
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It is justified to begin with the papers presented by Eckenfelder and Englande and by Benedek and
Farkas, because  the  temperature effects on reactions  and reaction rates in treatment plants (be
they of biological or chemical nature) are fundamental in our context.

It must be emphasized that we have to differentiate between:

- Temperature effects on the performance of the entire treatment plants or individual treatment
steps, and

- Temperature  effects  on single  chemical  or  physico-chemical  reactions or  reaction  chains,
including those occurring in organisms.

It would be a fundamental mistake to  confound these two groups of temperature effects. In the
case of, for instance,  a  biological  treatment  plant, the  temperature acts  preferably on the
population dynamics of the entire system. The resultant effect on plant performance is, therefore,
not  directly related  to temperature  functions (as  for instance  the Arrhenius equation)  of
biochemical reaction rates. It is true,  of course, that  the population shifts in mixed  continuous
fermentation systems  are caused by temperature  effects  on growth  rates  and  hence,  on
biochemical reaction rates. The phenomenologically dominant result, however, is a change in the
competition situation of the individual  species, leading to a so-called sociological adaptation of the
biocenosis (Wuhrmann,  1964). This change within the  organism  community must not necessarily
be associated with a shift in the overall fermentation performance.

In the paper of Eckenfelder and Englande temperature coefficients of numerous  activated sludge
laboratory and pilot plant experiments, as well as of lagoons are  compiled. The authors, and more
extensively Benedek and Farkas, stress the direct relationship of these observations with the van't
Hoff-Arrhenius equation  for  activation energy. It has  to  be  recognized, however, that these
temperature factors are  plainly empirical and should not be misused to anticipate the kinetics of
specific  biochemical  reactions.  The  temperature  coefficient  of  endogenous  and  substrate
respiration  of activated sludge has always been a favorite subject for studies and the essential body
of Benedek  and  Farkas' paper has many predecessors (Sawyer,  1939; Wuhrmann 1955, et al.). 0,0
values around 2 have been found consistently, from which E   values of about 11,200 -  12,000
kcal/mol (temp,  range  around 20°  C) may be calculated. Tnis figure is of little significance,
however, since we ignore completely the reaction that might be rate limiting within the observable
end result of oxygen consumption.  It is noticeable that other entirely different reaction chains
such as the  removal of a substrate from the medium (Benedek and Farkas) or the kill of bacteria
by disinfectants  (Chambers paper) are also subject to temperature effects with values of 0,0 in the
range of about 1.6 to 2.5 (calculated activation energies around 8,000 - 15,000 kcal/mol). This is a
general indication that enzymatically catalized reactions might be involved.  It is obvious, however,
that just because of this parallelism farther reaching conclusions  as to the behavior of complicated
systems such as living cells or entire organism associations are not justified.

There  is no  objection against the determination of temperature coefficients of plant performance.
Such  values are  very  useful in practice because they  give at  least a rough indication as to the
magnitude  of  safety  factors to be  considered  in the dimensioning  of biological reactors. It  is
pertinent, however, to clearly separate 1) reactions in a biological  treatment system which are
invariably affected by temperature changes according to thermodynamic  principles,  and 2) the
system's behavior as an entity under steady state conditions of  practical operation. The classical

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example for the first group of reactions is sludge respiration with a temperature factor 010  around
2. irrespective  of any other environmental  conditions or  population  shifts. It is mandatory,
therefore, to consider this temperature  factor in the dimensioning of aeration systems. Growth
rates as well as substrate resorption rates are subject to similar temperature factors. On a long term
basis of continuous operation and at slow temperature shifts, however, these temperature effects
will be largely hidden by a sociological adaptation of the sludge which may readily compensate for
the change  in  metabolic rates  of  the originally  dominating  species.  Most  sewage  plants
demonstrate, therefore, amazingly small  shifts of efficiency from summer to winter temperatures.
These small differences even disappear more or less completely  at low sludge loads (0.1 - 0.2 kg
BOD/kg dry  solids/day) because substrate supply and not temperature is then acting as the rate
limiting factor for sludge  metabolism. I think there is no  need for Eckenfelder's and Englande's
hypothesis,  assuming  sludge  flocculation is an  essential  parameter  for the  magnitude  of
temperature  effects  on the overall  performance of conventional  activated  sludge systems. This
hypothesis is even contradicted by earlier experimental evidence  such as Sawyer's  observations
(1955) and  the reviewer's  own results (Wuhrmann, 1964). The  idea of temperature-independent
rate limitations by too small a substrate supply is further confirmed by the skim milk experiments
in the paper of Koyama et al. and by the  laboratory experiments described by Clark et al.

The essential practical conclusions are therefore:

1.  Compensation for adverse effects of low temperature in activated sludge systems is readily
    possible by low sludge loads. With domestic sewage the limit is in the order of magnitude of
    0.1 to 0.2 kg BOD/kg MLSS/day. As was shown by the reviewer (Wuhrmann, 1964) and has
    been confirmed with the skillful experiments of Clark et al., dimensioning has to consider the
    lowest temperatures occurring.

2.  Aeration rates have to be evaluated on the basis of the highest temperatures to be expected in
    the system. Exigencies for low temperature will then automatically be satisfied.

3.  Although  lagooning  might be  a relatively  cheaper  investment than  other systems, it  is
    doubtful it will serve the needs, emphasizing the fact that the highest treatment efficiency is
    required in wintertime, i.e. at the lowest temperatures (see introduction of Gordon's paper).

The  above   conclusions  lead  to  some  technical  consequences  regarding  sewage and  plant
construction. From the operational point of view one of the main problems - especially with small
plants - is ice formation.  Heat conservation is imperative, therefore, and requests a very compact
and condensed plant layout.  Heavily exposed plants in the Alps of Switzerland are  enclosed for
protection against snow and wind and for easier  maintenance. The largest heat loss occurs in the
aeration basin due to evaporation and intensive exposure of  the water to the atmosphere. As has
already been mentioned by Pick and others, surface aerators should, therefore, not be used. Very
much can be done in favor of  safe plant operation with an adequate sewage system  as has neatly
been shown  in the paper of Koyama et al.  He  demonstrated how thawing may interfere with
treatment efficiency by  increasing the  hydraulic plant load and simultaneously decreasing the
sewage concentration and temperature. All three factors may work together  and produce an acute
danger of sludge  washout. The answer to this problem evidently  is separate sewering, a  concept
which is already adopted in the United States but still meets resistance in other places.

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Not  many  words have been devoted at this conference to the delicate topic of sludge treatment
and disposal, the paper of Balmer excepted. The problem is highly critical with small installations
where no machinery for sludge processing can be afforded. It is a favorable coincidence, however,
that  small  plants should be designed as very  low  loaded complete oxidation units, for reasons
already discussed. This concept automatically involves a minimum of excess sludge production and
a sludge quality  which is inoffensive, creates no odor problems and dries rapidly (especially after
freezing). Under these conditions the conventional drying bed is probably the optimum solution
for sludge disposal.

The  question of eutrophication by plant effluents has been discussed  in the papers  of Rosendahl
and  Balmer in regard to phosphorus removal from sewage. This is of course an immediate problem
all over the world. Irrespective of the obvious question of whether nutrient removal from wastes is
of top priority in the Alaskan situation, the process described by Balmer raises an interesting point
worth mentioning:  chemical  processes such as precipitation or adsorption etc. have much lower
temperature  coefficients (diffusion being  mostly  the  rate-limiting process)  than enzymatically
catalized reactions.  Dimensions and  operations of  chemical  purification plants are much less
affected, therefore, by temperature shifts than are biological units. This represents a considerable
advantage.  In view of the high degree  of purification required by  the winter conditions in arctic
rivers, it  is questionable, however,  whether exclusively chemical processes as described by Balmer,
are sufficiently effective in regard to removal  of dissolved organic  compounds. It is also common
experience that handling of excess sludge from precipitation units can be  a difficult task. I am of
the opinion, therefore,  that the application of chemical precipitation or flocculation processes
under  critical operation conditions (small plants, low temperature,  unskilled  personnel, etc.)
should be considered with caution.


                                       REFERENCES

Sawyer, C. N. (1939) Factors  involved in prolonging the initial high rate of oxygen  utilization by
     activated sludge - sewage mixtures. Sew. Wks. J., 11, 595.

Sawyer, C. N., Frame, J. D. and Wold, J. P. (1955)  Revised concepts on biological treatment Sew
     Ind. Wastes, 27, 929.

Wuhrmann, K. (1956) Factors affecting efficiency and solids production in the activated sludge
     process,  Biol.  Treatment of  Sewage  and Industrial Wastes, Vol. 1,  49-65,  Reinhold Publ.
     Comp. New York.

Wuhrmann, K. (1964) Bibl. Microbiol. Fasc., 4, 52-64.

Wuhrmann, K. (1964-68) Hauptwirkungen und Wechselwirkungen einiger Betriebsparameter im
     Belebtschlammsystem.  Ergebnisse mehrjahriger Grossversuche,  Schweiz. Z.  Hydro!., 26,
     218-270, see also Adv. in Water Quality Improvement, Univ. Texas Press, p. 143.

                                               * U. S. GOVERNMENT PRINTING OFFICE; 1912 O - 454-699

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