United States       Environmental Research    EPA 600 3-79-102
        Environmental Protection    Laboratory        September 1979
        Agency         Corvallis OR 97330
        Research and Development
        Management of
        Bottom Sediments
        Containing Toxic
        Substances

        Proceedings of  the
        Fourth U.S.—Japan
        Experts' Meeting
        October 1978
        Tokyo, Japan
      ^JH
EPA/600/3-79/102

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                RESEARCH REPORTING SERIES

Research reports of the Office of Research and Development  U S  Environmental
Protection Agency have been grouped into nine series  These nine broad cate-
gories were established to facilitate further development and application of en-
vironmental technology  Elimination of traditional grouping was  consciously
planned to foster technology transfer and a maximum interface m related fields
The nine series  are

      1   Environmental  Healtn Effects Research
      2   Environmental  Protection Technology
      3   Ecological Research
      4   Environmental  Monitoring
      5   Socioeconomic Environmental  Studies
      6   Scientific and Technical Assessment Reports (STAR)
      7   Interagency  Energy-Environment Research and Development
      8    Special  Reports
      9   Miscellaneous Reports

This report has been assigned to the ECOLOGICAL RESEARCH series This series
describes research on  the effects of pollution on humans plant and animal spe-
cies, and materials Problems are assessed for their long- and short-term mflu-
ences Investigations include formation transport and pathway studies to deter-
mine the fate of pollutants and their effects This work provides the technical basis
for setting standards to minimize undesirable changes in living organisms in the
aquatic, terrestrial, and atmospheric environments
This document is available to the public through the National Technical informa-
tion Service, Springfield, Virginia  22161

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MANAGEMENT OF BOTTOM SEDIMENTS CONTAINING TOXIC SUBSTANCES

   Proceedings of the Fourth U.S.-Japan Experts'  Meeting
                October 1978--Tokyo, Japan
                         edited by

         Spencer A.  Peterson and Karen K.  Randolph
        Corvallis Environmental Research Laboratory
                  Corvallis, Oregon 97330
        CORVALLIS ENVIRONMENTAL RESEARCH LABORATORY
            OFFICE OF RESEARCH AND DEVELOPMENT
           U.S.  ENVIRONMENTAL PROTECTION AGENCY
                  CORVALLIS, OREGON 97330

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                                  DISCLAIMER

     This  report  has  been  reviewed by  the Corvallis  Environmental  Research
Laboratory, U.S.  Environmental  Protection  Agency,  and approved  for publica-
tion.   Mention  of  trade names  or  commercial  products  does  not  constitute
endorsement or recommendation for use.

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                                   FOREWORD

     Effective regulatory  and enforcement  actions  by the  Environmental  Pro-
tection Agency would  be  virtually impossible without sound scientific data on
pollutants  and  their impact  on  environmental  stability  and human  health.
Responsibility for building  this  data base has been  assigned  to  EPA's Office
of Research and Development and its 15 major field installations,  one of which
is the Corvallis  Environmental Research Laboratory (CERL).

     The  primary  mission of  the  Corvallis Laboratory is  research  on  the  ef-
fects  of  environmental  pollutants  on  terrestrial,  freshwater,   and  marine
ecosystems;  the  behavior,  effects and  control   of  pollutants  in   lakes  and
streams; and  the  development of predictive models on  the  movements of pollu-
tants  in  the  biosphere.    In  May  1974  the  United   States-Japan  Ministerial
Agreement  provided  for the  exchange  of environmental information  on several
areas of  mutual  concern.   This report is  the  compilation  of papers presented
at the  Fourth U.S.-Japan  Experts'  Meeting on the Management  of  Bottom Sedi-
ments Containing Toxic Substances which  was held October  30-November  3,  1978
in Tokyo.
                                                       Thomas A.  Murphy
                                                       Director,  CERL

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                                   CONTENTS

JAPANESE PAPERS

Dredging and Treatment of Sediments in the Port of Tagonoura
     Toji Inada	   1

The Improvement of Water Quality at Lake Kasumigaura
by the Dredging of Polluted Sediments
     Mineo Matsubara	11

Lake Suwa Water Pollution Control Projects
     Akira Sakakibara and Osamu Hayashi 	  31

Dredging of Polluted Bottom Sediments in the Ibo River
     Sadao Kishimoto	65

Pollution Control  in Tokyo Bay
     Masai Yako and Keitchi Akimoto	91

Release of Nutrients from Lake Sediments
     Ken Murakami  and Kiyoshi Hasegawa	127

Test Results from Demonstration Dredging and
Spillwater Treatment at Hiro Harbor
     Toshihiko Fukushima and Tathuo Yoshida	143

The Contribution of Sediment to Lake Eutrophication
as Determined by Algal Assay
     Ryuichi Sudo and Mitsumasa Okada	161

Toxic Material and Nutrients from Contaminated Sediments
     Yoshiharu Nakazono and Yasuji Saotome	181

The Filtering Effect of Containment Walls on Supernatant
from Contaminated Dredge Material
     Takeshi Monji	207

Accumulation of Mercury by Fish from Contaminated Sediments
     R.  Hirota, M. Fujiki, Y. Ikegaki and S.  Tajima	225

UNITED STATES PAPERS

Approaches for Mitigating the Kepone Contamination
in the Hopewel1/James River Area of Virginia
     K.  M. Mackenthun, M. W. Brossman, J.  A.  Kohler, and C. R. Terrell. .  .241

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                                CONTENTS (cont)

PCB Contamination of the Sheboygan River, Indiana Harbor
and Saginaw River and Bay
     Karl E.  Bremer	261

Developmental Aspects and Current Policies for Restoration and
Protection of Publicly Owned Freshwater Lakes in the United States
     Spencer A.  Peterson and Robert J.  Johnson	289

Sediments and Sediment Disturbance During Dredging
     John F.  Sustar	311

Bioaccumulation of Toxic Substances from Contaminated Sediments
by Fish and Benthic Organisms
     Robert M.  Engler	325

Management of Containment Areas to Promote Dewatering and Solidification
     C. C. Calhoun, Jr	355

Impacts of Oil  Spill and Clean-up on the European Coast:  Amoco Cadiz
     William P.  Davis	371

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         DREDGING AND TREATMENT OF SEDIMENTS IN THE PORT OF TAGONOURA

                                  Toji Inada
          Chief, Port and Harbor Section, Civil Engineering Division
                    Shizuoka Prefectural  Government, Japan
                                 INTRODUCTION

     The paper industry in the Gakunan district near the Port of Tagonoura has
prospered by using the extensive water and forest resources at the foot of Mt.
Fuji.   The  industry  began  manufacturing  paper about  90 years  ago  and  has
expanded through mechanization and integration of smaller businesses.

     After  World  War  II,  many  enterprises  such  as  Nissan Motor  Company,
Toshiba  Electric Company,  and  Asahi Chemical  Industry Company, built  large
factories in  this district.  Now  there are  1,300  factories  producing paper,
pulp,   foods,  machines  and  metal  merchandise.  The  opening  of  the  Port  of
Tagonoura in 1961 improved cargo transportation.  Construction of the man made
port started in  1958.  It accomodates 10,000 ton-class ships.

     The industrial output  in this  district  is  950 billion  yen,  of which 47%
is produced  by   the paper,  pulp and paper-processing industry — the largest
such group  in  Japan.    The  factories use  about  2.0  x 106 m3 of  water a day.
Sewage drains  into the Port  of  Tagonoura  via the Numa  River, the  Urui  River
and the Gakunan  drainage basin.   Suspended solids (SS) from the sewage accumu-
late on the bottom of the port.

     The sewage  sludge is  called  "hedoro"  in Japanese.  In  1970,  1.2  x 106
metric tons of  Hedoro was discharged into the environment.  The sludge spread
and  interfered   with  port  functions.   It produced toxic  H2S gas.    The odor
became a public  nuisance.

     The first management effort, in 1971, was to remove the sludge.  The plan
was to use  self-propelling  barges  to dump the sludge  in the open sea, 320 km
from the Port of Tagonoura.   The barge hulls were reinforced and remodeled to
carry sludge.

     Before the  plan could be activated it was opposed by fishermen  and scien-
tists who had attended the World Oceanography Congress,  and therefore the plan
had to  be changed.  On-land treatment was the only alternative.

     On-land treatment  creates  problems on how to dehydrate the sediments and
avoid  secondary  public nuisances from  unpleasant odors,  toxic  gases produced
by the dehydration process and contamination of groundwater by infiltration of
polluted water.    The  dry bed of the  Fuji river was selected  as a treatment
site since  it had extensive area available  for mass dehydration.

                                       1

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     The bottom sediments were first dredged using a cutterless suction dredge
to minimize sediment agitation.  Sediments  were  loaded on a barge and carried
to the  mouth  of the Fuji River where  they  were  pumped to  a  dehydration  pond
via pipeline.

     With this  system  the  first  management  effort dehydrated  110,000  tons  of
sediment at a  cost  of  820 million yen.  Since the capacity of the dehydration
pond had been  determined,  the second and third mass  management effort used a
bigger suction dredge.

     The second and third management  efforts were  implemented from  1972  to
1974.    The  sediment was  dredged  by a  5,000 ps  suction dredge  and  carried
directly to the dehydration  pond on the dry  bed  of the  Fuji  River  through a
pipe 6 km long.  Natural dehydration then occurred.

     The system was continually  improved.   Steel-covers  were installed on the
upper part of the outside of  the  cutter so  the sediment would not be  dispersed
through agitation.  Fishing nets  were used  to cover the dredging area to avoid
contamination  of  the  sea.   The  pipes  for  carrying sediments  were  pressure
tested  at  15   kg/cm2 which exceeded the  maximum  pressure of  the dredge pump.
Pressure gauges were   installed at each  kilometer  of pipe  and readings  were
monitored and  telephoned to the dredge tender.

     A Ca(OH)2  solution of 1,500  ppm was  injected  into the pipe during transit
to remove H2S.  A FeCl3 solution  (39%) of 333 ppm  was added to adjust the pH
value.   A  high molecular  cohesion agent of  10   ppm  was  added  to accelerate
dehydration.    Finally,  an  aeration  tank was  installed at  the  pipe  outlet to
remove any remaining H2S gas.

     The sediment's  water content  was  about 98% before  dehydration  and was
reduced to about  80%  after natural drying in the dehydration pond.  The dehy-
drated sediments were reclaimed after mixing with  gravel  and cobblestones from
the dry river  bed in a ratio of one to one.  This was done with a bulldozer.

     A total  of 1.3 x 106 m3  of sediment  was removed by these three management
efforts.   During  the   same  period,  effluent standards  were  established  to
control the source  of  wastewater.   These standards were raised  four times.  As
a  result, new accumulations  of sludge have decreased, however 5.2 x 105 m3 of
sediment still  remained in  1975.   If the  sediment had  been  left as  it was,
pollution  would recur.   Therefore, a fourth sediment management effort was
scheduled to  be implemented by the Public  Nuisance  Countermeasure Council.

     This  paper  reports   on  the   fourth  management  effort  in  the  Port  of
Tagonoura.


                            FOURTH  MANGEMENT EFFORT

PROPERTIES OF THE  SEDIMENT

     The properties  of the sediment were:   muddy sludge,  20.4% average  igni-
tion-loss (ash-free dry weight),  70-80%  water content, an  infinitesimal  quan-

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tity of heavy-metal,  and  an average value of  28.5  ppm of PCBs.  The PCB con-
tent had been  decreased  by the more stringent regulation of water quality and
the prohibition on  using  PCB-containing copy paper as toilet tissue.  The PCB
could not be  detected by an elution test.  Taking all matters into considera-
tion, the plan  was  to remove only the sediment containing PCB in excess of 10
ppm or with an ignition loss of more  than 15%.

PLANNING

     Since on-land  management was  mandatory,  the adjacent  right  fork  of the
dry Fuji River  and  a timber pond in Port Tagonoura were selected as the land-
fill areas.   The timber  pond was chosen because the sediment could be used as
fill material  in a  separate project to remodel  the  pond into a timber depot.
The  right  folk of  the  dry  river  bed was selected  for  two reasons.   First,
reclamation of  the  sediment in the left  fork  of the dry river bed had proven
to be safe  and effective.   Second,  a sporting  arena  to  be constructed on the
reclaimed ground of  the left fork had gained consideable public favor.

     Engineering methods were studied which could do this project inexpensive-
ly, effectively and safely, and without creating any secondary public nuisance
factors.

     A  big  suction  dredge  and natural dehydration  was  considered.  But, the
system  was discarded  for  the following reasons.  First, the right  fork of the
river bed was narrower than the left fork and, consequently, limited the space
for dehydration ponds,  thus restricting the working  hours  of the  big suction
dredge  and  lowering  the  efficiency of the whole  system.   Second,  the dredge
discharge pipe  was  vulnerable to flood  damage since it would  have to  be in-
stalled across  the  river.  Third, the system carried a risk of polluting water
supplies near  the right  fork of the dry  riverbed.   Fourth,  the natural dehy-
dration method  could  not  be used in the  timber pond area since the pond con-
tained  too  much water and noxious  odors from  the sediment  would pollute the
residential  zone around the pond.

     Next, methods  of mechanical  dehydration  instead of  natural  dehydration
were examined.  These methods  had  been widely  used in the wastewater disposal
plants  of  the  paper factories.   But, this  method  was found  unsuitable by
experiments which showed  that the  equipment would be corroded by seawater and
screens broken  by materials such as vinyl, wire, blocks of wood, or any earth
and sand carried downstream from large washouts near Mt. Fuji.

METHOD OF TREATMENT

     Because of the above  problems, a system using rented machinery requiring
little  capital  investment  was adopted.   This method picked up highly-polluted
sediments with  a grab dredge and added agents to dehydrate and solidify them.
We started to  look for processing agents for this system.

     Quicklime was  first  considered because  it  has  been used successfully to
strengthen weak soils.   Quicklime  absorbs  32%  of  its  weight  in water and
quicklime-enforced  sludge  is stable over time.   Results of these  experiments
showed  that a  72.5% water content in the sediment decreased linearly to 62.2%

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10 minutes after the the addition of 5% quicklime and to 5.9% 10 minutes after
the addition of  10% quicklime,  and that the addition of 20% quicklime solidi-
fied the sediment enough to make it suitable  for reclamation soil.

     Although the problem  of  controlling lime dust and  vapor  produced by the
reaction was trivial  in  the laboratory, the problem  could  not be ignored for
large  scale  use  involving several  tons  of quicklime.   Different  approaches
were considered, including  mixing with scrapers in enclosed barge  and mixing
under  an  air curtain  created by  a  power blower installed  on  the  barge.   No
completely satisfactory perfect  answer was  found.   In addition to this, there
was another  problem.   Mixing  of  the quicklime solution had to  take  place very
rapidly because of the tendency for quicklime to solidify immediately.

     As a result of the number and complexity of these problems, quicklime was
discarded as a  hardening  agent.   When selecting the proper agent, the follow-
ing characteristics  were considered:

     1.   The  solidifying  agent  must strengthen the  mixed sediment  to  more
than 1.0  kg/cm2 of  uniaxial  compression  strength  (referred to as  DCS)  so it
can be  worked  by a  swamp bulldozer during reclamation.  Although the ordinary
load for a swamp bulldozer is 0.3 kg/cm2, a standard of 1.0 kg/cm2 was adopted
for safety.

     2.   It must be easily mixed.

     3.   It should  not produce any dust or fumes during mixing.

     4.   No harmful  substance  should  be  detectable and  no secondary public
nuisance factors should be created by it.

     5.   It must be economical.

     More than  1500 combinations  of 40 kinds of material were  tested, includ-
ing solicic  acid soda,  volcanic  ash, cements,  plasters, incineration ash, and
some dehydration agents  developed by private companies.  A combination of 12%
cement, 5% incineration  ash and  4% exhaust-gas-desulfurization-plaster (EGDP)
was selected.  The  following  three ingredients  - aluminum  in  the ash (A1203,
50-58%), calcium in the EGDP  (CaS04-2H20)  and  calcium in  the  cement - dehy-
drate and promote solidification of the high-water content  sediments.

     Incineration ash  can  be  produced by  nearby  paper  factories.   The  EGDP
could  be obtained from factories  at the port.  Both of these are waste and can
be  purchased  inexpensively.   Later  research  determined  that   good  quality
incineration ash to  meet  environmental  standards could  not  be produced in
sufficient volume.    As a  result,  fly ash cement [referred  to  as FA (B-type)]
was  used instead of incineration ash  and  it was  necessary to  increase  its
volume to 13% to  make the required DCS  (Figure 1).

     The UCS of the sediment 48 hours after the  addition of 4%  EGDP  and 13% of
various kinds  of cements  showed  good values of 0.8 kg/cm2 for  FA (A-type) and
1.12 kg/cm2  for FA  (B-type), which  are better  than the  value  of 0.68 kg/cm2
for  normal   Portland cement.   Consequently,  it was  found  that including  a

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                             1.5



                             1.0

                          UCS


                            0.5

                        kg/cm2
                                                              o
                                                                 -o
                                                     72 hours after
                                                   • 48 hours after
                                                   o 24 hours after
                                            J_
                                                     I
                                                              1
                                                                  1
        FA (B type) (%)9   10
        EG DP       2.7  3.0
   surf ace active agent    0.08 0.08
W/C (water cement ratio)    70  70
W/C of the raw sediment
                                             II   12  13  14
                                            4.0 40  40  4.0
                                            0.08 0.08 0.08  0.08
                                            70  70  70  70
                                                              15   16
                                                             4.5  4.8
                                                             008 008
                                                             70  70
             Figure 1
    1.5


 UCS

    1.0
   0.5
kg/cm2
                                   78.01 78.01 78.01 78.01 78OI 78.01 7801 78.01
                                 (surface active agent  cement volume X 008%)
                          Comparison of uniaxial  compression strength
                          (UCS)  for various combinations.
                          72 hours after
                   O	O 48 hours after
                   O	O 24 hours after
          O-..
                        	O
               ••p.	A,	O
                                  1.0
                                             UCS
                                               0.5
         F.A.   FA. normal    processing
        BtVDe AtVD Portland   agent by
                   cement    Mitsubishi Co.
Figure  2.   Strength by  annexations  of
            various  kinds  of cements.
kg/cm2
O—O 72 hours after-
O—-O 48 hours after'
O	o 24 hours after"
                                              5
                                            EGDP
 10
                                                 Figure 3.   Strength by the annexa-
                                                             tion of EGDP.
     1.5


  UCS

     1.0



    0.5
kg/fcm2
          I
                              i
                          72 hours after.
                       -• 48 hours after
                       •O 24 hours after
                                     1.0

                                  UCS

                                     0.5
        60           100
             water cement ratio
     Figure 4.   UCS for W/C
                                                                 i
                                                                            hours after
                                                                  •	ป48 hours after
                                                                  O-	-O24 hours after
                                kg/cmx|  0.000.040.06008 o.io
                                            surface active agent
                                           (cement volume x %)
                             Figure 5.   UCS for  surface  active  agent.

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suitable  quantity  of  the fly  ash solidifys  and  strengthens  sediment  which
contains  a  large  quantity of  paper  sludge  (Figure  2).   The  most  effective
mixing ratio of the EGDP was found at 4% (Figure 3).

     To add the  agents, the cement and  EGDP  at a 70% water-cement  ratio was
mixed with  the  surface  active  agent  to promote  hydration.   The  water-cement
ratio was selected by  considering the efficiency of machinery,  reactivity and
dust prevention (Figure  4).  Compared  to no additive, the UCS  was  doubled by
the addition of 0.08% surface active agent to the cement's volume  (Figure 5).

     These experiments  showed the combinations of 13% FA (B-type) and 4% EGDP
to the weight  of the  sediment,  and 0.08% surface active agent to the weight of
the cement was the proper combination for  this program.

IMPLEMENTATION

     Ideally,  the methodology works like this:  The sediment  dredged by a grab
dredge should be carried by  a barge to  the quay wall, and  it  should  then be
mixed with the processing agents.  Next,  the  mixed sediment  should  be  hauled
by dump trucks to the reclamation site  (Figure 6).

     The  processing  volume per  day was planned  at about 1,100  m3  based on
considerations of economics and  efficiency;  namely, the holding capacities of
the  temporary depots,  the mixing plant and the  spillwater-processing appara-
tus  as  well  as the  impacts on  neighboring activities created by  the  noise,
traffic tieups caused by  dump trucks, etc.

     The management project in  1977,  where sediment was reclaimed only in the
timber pond, was conducted as described below:

Dredging Work

     A  6  m3 bucket  dredge enabled the  management of  1,100 m3  sediment per
8-hour  day  in a program cycle  of  dredging,  mixing  and  temporary  detention.
Four closed-bottom box  type barges with 500 m3 of loading capacity were used.
This allowed for a 20% volume  increase after mixing the processing agents into
350 m3 of  dredged sediment.

     To prevent pollution  of  nearby areas caused by turbulence  and release of
sludge from the grab,  control  measures were selected carefully.  This problem
is most important  in  management of secondary public nuisance factors.  There-
fore, a silt curtain was laid in the sea surrounding the dredging site (Figure
6).

     The curtain was  made of  soft vinyl-covered canvas  which could withstand
the  range  of  tides.   Steel had  been  considered as a  curtain material  but it
was  discarded  since  the height could not  be  changed at the ebb tide  and it
could not be easily moved.

     The 50 kg  anchors  with chain ballasts were installed at the lower end of
the  curtain to  enable the curtain to  conform to the contour of  the uneven sea
floor.   Since the curtain is  lowered as the sea-bottom is deepened by dredg-
ing, seawater  inside the curtain cannot flow to the outside.

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               DREDGING
              MIXING AND LANDING
                       \mixing plant
                       n  I   stock bin for EGDP
         6.0 M  a grab dredger
 a floating
 frame
               a suspended curtain

                iซ200 pipes
injection
equipment
     500 M
                50kg Anchor with chain ballast
                                            CONVEYANCE AND RECLAIMING
      sediment
                                                             fence to prevent pollutions
                                                                         ''"
                          Figure 6.   Treatment program.
     The  shape  of the vertical  section of  the  curtain was  a  trapezoid:  10 m
for the upper part,  18 m for the middle and 28  m  for the  lower part.   Approxi-
mately  500  m3   of  sediment  was  expected  to  be  dredged  from  each  curtain
shrouded  site.  Two  sets of curtains and frames were constantly employed.  The
curtain was moved  to  the next site after dredging was  completed at  the initial
site.   Each curtain  was moved  only  after adding 3  ppm of  coagulation agent to
precipitate the suspended solids inside the curtain.

     No abnormal  signs were  observed at observation points  around  the curtain
during  dredging.   The  curtain  effectively  prevented  pollution.   Emission  of
the offensive  odor  of H2S  gas was  negligible because the dredging  was done
during the  cool  season.   Also,  hypochlorous acid soda was  sprayed for desul-
furization and deodorization.  As a result,  no air was polluted.

     The  average  dredging  time  required to  load  350 m3 of  sediment  onto  a
barge was  2h  hours.   This  entailed  90 grabs.   The  efficiency  of the  grab was
good because  the  water  content  of  sediment  decreased as  dredging  depth in-
creased.

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Mixing the Sediments with the Processing Agents

     The processing  agents were mixed  in a  plant installed behind  the quay
wall.   The mixing process  was  mechanized and controlled at  a  single  station.
In  the  process,  EGDP and  water were  combined to  allow  a 70%  water-cement
ratio.   Then cement and  activator were  weighed and mixed  in by  a 1-m3 turbo-
mixer.   Next, the mixed  agents  were  injected into the sediment while  still  in
the barge.  The time required from weighing to injection was about one minute.
The mixing could  be  done almost continuously because  every  batch was removed
by pump  after temporary detention in the  storage chambers.

     Since the water  content  varied  with every batch of dredged sediment, and
since the  water-cement  ratio  affects  the  DCS,  it  is necessary  to quickly
determine  how  much  cement to  add  to  the  mix.   The water-cement ratio was
determined from  the water-content value  measured either  by a  Kett moisture-
measuring  instrument  or  by comparison  with the  water content  of sediments
gathered in test dredging.

     As  a  result  of testing, it was proven  feasible to be  within  65% of the
average  water-cement  ratio  since  the precise value of  the latter measurement
was close  to the measured value and also since  the water content  had been
homogenized  by the  narrowness  of the dredging area  and by drainage of exces-
sive water from the barge.

     Two clamshells were  used  to mix the sediment with the solidifying agents
on  the  barge.   The mixing  took about 2 hours per barge (350  m3).  This time
was determined from data on the strength of the mix relative to the frequency
of  mixing,   as  found  by  experiments  and observations  at  the  job  site.   The
value of the DCS  measured at the job site after 48 hours  was  0.3~1.0 kg/cm2.
Soft sediments were  strengthened by extending the temporary  detention time.

     The mixed  sediment was  temporarily  detained for 24  hours  in  the barge,
and again  detained  for  24 hours after  unloading.  The  sediment  was then car-
ried to the  reclamation  area.   The  vicinity was free of pollution because the
emission of noxious  odors  and H2S gas  was minimized by the mixing.

     After some accidents occurred  where the bottom  of  the  barge was damaged
by  an  unskilled grab operator,  it  was  necessary to  reinforce  the  bottoms  of
the barges.

Reclamation Work

     Our policy  was  to  avoid exudation  of  sediments.   The open part of the
timber  pond  was coffered with steel sheet piles, back-filled  with fine sand
and covered  with  vinyl  sheets.   All  the  levees  of  the pond were covered with
vinyl sheets  even  though  they were considered safe.

     It was  estimated that pollution of  groundwater  would not  occur  because:
The bottom of  the pond  had a  good  clay layer; no percolation happened in the
experiments; the sediment to be reclaimed was safe because no harmful  substan-
ces  had been detected  in it;  and the  sediment  would be gradually solidified
with chemical agents.  To make doubly sure, several wells were sunk around the

-------
pond and  the quality  of  the underground  water was  monitored  throughout the
reclamation project.

     The sediments were pushed  out from a side levee using a swamp bulldozer,
because  the sediments  should  settle  in  the  water  of  the pond.   The  water
surface was covered with vinyl sheets to prevent the escape of offensive odors
and  H2S  gas.  Some  hypochlorous acid  soda  was sprayed  under  the  sheets  to
neutralize odors  and gas.

     The draining  of the  wastewater from the  pond after  treatment was done
concurrently with progress of the reclamation project.  A settling pond 5 m by
125 m was  built  in the pond.  About 2.0  ppm of cohesion agent and 500 ppm of
FeCl3 (to  ajust  the  pH value) were injected into the wastewater at the inlet.
The solid  materials  in the wastewater coagulated and settled in the main pond
and the water was then drained outside the pond after rapid filtration through
a sand bed.

     Water quality of the outflow was constantly monitored by measuring trans-
parency.   Acceptable values were determined by the correlation of experimental
values of  transparency relative  to SS and  PCB.  No elution of PCB was detected
by later analysis.  This demonstrated the efficacy of the methods.

     Some  sediment from  the bottom of  the timber  pond  was brought  to the
surface  during  the reclamation.  We treated the sediments  by  mixing 13% ce-
ment, 4% EGDP and 0.08% activator.

     The reclaimed  ground was  soon  available  as  a timber  depot because its
firmness had increased from  3.9~13/0  kg/cm2 after  only 2  months.   Work was
done from  March,  1977  to  May,  1977  and  from October, 1977 to December, 1977,
thus avoiding the production of  gases in summer.  In this project 15,000 m3 of
sediment was reclaimed in  the  timber pond  at  a cost of 790 million yen,  of
which 2,160  yen  per  1  m3 of  sediment was  for the cement and chemical agents.
The cost  does  not include  the  expenses of bank protection  and finishing the
reclaimed ground.

Supervision Plan

     This work was supervised under the provision of "A Tentative Guide to the
Management  of Sediments"  issued by the Director General  of the Environmental
Agency of  Japan.   Basic observation  stations were established at the mouth of
the port to  monitor seawater quality.  A supplementary observation station was
set up  to   allow  estimates  of  water quality changes at  the main observation
station.   This permitted  stop/proceed decisions on  dredging.   Also, stations
for monitoring air pollution were established.   The Life Environment Division
and the  Agriculture  and  Fishery Division of  Shizuoka  Prefectural  Government
took the  observations at these stations.

     The observed  items  and the  standards  for action  are given  below.   No
abnormal  values were observed.

-------
      Station
                        Observation  Items
Frequency
 Standard Values
   for Action
Basic
                        pH,  DO,  COD

                        SS,  Cl

                        transparency

                        PCB,  Hg
   I/day      COD not exceeding
                8 ppm
     "        PCB should not be
                detected
     "        Gross Hg 0.0005
                ppm
     "        transparency 7 cm
                or more
Supplementary
Outlet of drainage
transparency
PCB
transparency
4/day
I/day
7 cm or more
0.01 ppm
proportional to
                                                              the  above  value
Underground Water
                        PCB

                        H2S
                                                 I/day

                                              continuous
              should not be
                detected
              should not con-
                tinue for 2
                hours or more
                at 0.2 ppm at 2
                points at the
                same time
Air
                        weather conditions
                        PCB
continuous
  2/month
not exceeding 0.5
  ug/cm3
Fishes & Shellfish
                        PCB
              not exceeding 3
                ppm
                                  CONCLUSION

     The  result  of  this  sediment management  effort was  the  test which,  if
successful, would permit  the  treatment of  the remaining 370,000 m3  of sedi-
ment.   The excellent  outcome,  which  created  no  secondary  public  nuisance
factors,  was  a  result of  the  refinement of  techniques  to prevent  seawater
pollution, H2S gas and offensive odors.

     If a  large  depot  for temporary  detention can be secured  or sediments can
be reclaimed on  land, it is anticipated that expenses and quantities of cement
and EGDP can be reduced.

                                   REFERENCE

Ichikawa, Takashi.  The Management of  Sediments  of the Port Tagonoura

                                      10

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              THE IMPROVEMENT OF WATER QUALITY AT LAKE KASUMIGAURA
                     BY THE DREDGING OF POLLUTED SEDIMENTS

                                Mineo Matsubara
          Kasumigaura Work Office, Kanto Regional Construction Bureau
                        Ministry of Construction, Japan


                                    LOCALE

LAKE KASUMIGAURA

     Lake Kasumigaura  is  the  second largest lake in  Japan  (Figure 1).   It is
located  northeast  of the  Tokyo metropolitan area at  the southeastern  end of
Ibaragi  Prefecture.   It actually consists  of  three  lakes:   Nishiura,  Kitaura
and  Sotonasakaura.    Nishiura   Lake  drains  into Lake  Sotonasakaura via  the
Kitatone River,  and  Kitaura Lake drains into  Lake Sotonasakaura  via the Wani
River.   Sotonasakaura  Lake is  connected  with the Tone River  via the  Hitachi
River at a point  18 km from the Pacific Ocean.

     Lake Nishiura covers  171  km2 and Lake  Kitaura  covers  34 km2.  The total
area of  Lake  Kasumigaura,  including Lake Sotonasakura and the rivers is about
220  km2.  The average depth of  the  lakes  is 4  m.  The deepest spot does not
exceed more  than  7 m.   It is too  shallow to maintain high water quality.

     The average water  level  is approximately Y.P 1  m (the average sea water
level +  16  cm).  The  lake  volume  is about 800 million.  The  lake used to be an
inlet of the  sea divided by the  Kashima plateau.  Then the  mouth  of the inlet
was  closed  by sand  and soil deposited  by the  Tone  River.   The  water  of the
present lake therefore is a mixture of fresh water and sea water.

DRAINAGE BASIN

     The area  of the Kasumigaura basin is  2169  square kilometers - about 35%
of  Ibaragi  Prefecture  (Figure  2).   The basin  consists  of  the  hilly country
between  20  and 30 m  above  sea  level  and the rice fields extending along the
coastal  region of  Lake Kasumigaura, except  for  parts  of  Mount Tsukuba (876 m
elev.),  Mount Ashio  (628  m  elev.) and  Mount  Kaba  (709 m elev.)  which are
located  along the reaches  of the Sakura  and Koise Rivers  which  flow  to Lake
Nishiura.

     The average annual rainfall  is  1350  mm.   This  produces  an  annual  water
input of  1.2 x  109  m3  to  Lake  Kasumigaura.  Dividing this volume by  the ap-
proximate capacity of the lake yields an annual  replacement rate of 1.5 times.
                                      11

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       40'
30ฐ
         130ฐ
135ฐ
140ฐ
       Figure 1.  The  location of Lake Kasumigaura in Japan.





                                  12

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TSUKUBAStudy
and Education
City
SUOHIURA
                                                           Kashima

                                                                Kashima
                                                                Port
                                                               •Hatachi
                                                                River
                                                                  luice
                                                                  kGatex
                             International
                             Airport
                                              rYOKAICHJฃ/

      Figure 2.   Lake  Kasumigaura and its drainage basin.
                               13

-------
     More  than  fifty  rivers including  the  Ono, the  Sakura,  the  Koise,  the
Sonobe, and the Tomoe  flow into Lake Kasumigaura,  while only the Hitachi Tone
River  (the  Kita Tone  River and the  Hitachi  River  are  generally known as "the
Hitachi Tone  River")  flows  out of  this  lake.   The Hitachi Tone  River  has a
complicated hydraulic mechanism because  the  slope  of the river bed is gentle.
The water  level is  affected by that of the Tone River, which is influenced by
tidal levels.

     The  basin  area  includes  47  cities,  towns and villages  in  Ibaragi  and
Chiba  Prefectures.   The  population of  this area  is  estimated  at  720,000.
Agriculture is  the  biggest  industry in  the  region.   This is one  of  the most
prominent regions  in Japan for hog farming and carp rearing.

     Large-scale projects  undertaken in  this area  include the  Kashima Coastal
Industrial Zone in  the  eastern  part of  Kasumigaura  and  the Tsukuba Study and
Educational Institution  in  the western region.

     At Kasumigaura, the  Kasumigaura Development Project is starting  to cope
with the  increased  demand  for  water by  the metropolis.  By  1983, when this
project is  completed, water resources  of 40  m3/S will  be developed by utiliz-
ing the 2.6 x  108 m3  available between the water levels of Y.P 1.30 m and Y.P
0 m.

     The  lake  will  become  a  freshwater  lake  by  temporarily  employing  the
Hitachi  River  Sluice  Gate  to  prevent tidal  intrusion  upriver.   This  sluice
gate,  at  the  juncture  of  the   Hitachi and the  Tone Rivers, was completed in
1963.

     Thus,  since  the  lake  has  been resurrected as  a  storage  reservoir,  the
maintenance of good water quality is very  important.

              CONSERVATION OF WATER QUALITY IN LAKE  KASUMIGAURA

WATER QUALITY  AT THE PRESENT TIME

     The water quality standard for Lake  Kasumigaura was established in Novem-
ber, 1972  as  "type  A-(c),  COD  3.0 ppm,  provisional  standard type B,  COD 5.0
ppm" for  the  lakes  and  marshes in the  area of Kasumigaura,  Kitaura (including
the Wani River) and the Hitachi  Tone River.

     The average  figures  for 1977 water  quality, measured  at  eight places in
Kasumigaura, are given  in Table 1.  Observation  points  are indicated in Figure
3.   The  COD,  which  is the  typical  index  for water  quality  of lakes  and
marshes,  is  between 6.0  ppm and 7.9 ppm.  This is  considerably greater than
the 3.0 ppm which is the standard for Kasumigaura. (Figure 4)

     T-N  and  T-P, which are indices of  eutrophication,  are 0.77  ppm to 1.25
ppm  and 0.04  ppm  to 0.08 ppm,  respectively.   Both  of these figures exceed the
general standards  of 0.15 ppm T-N and 0.02 ppm T-P.

     Past  changes  in  water  quality are   not well  known  because the  data are
insufficient.   However,  a deterioration of the water quality has been conspic-


                                      14

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uous  since  1968.   Eutrophication of  the lake has  developed  rapidly.   In the
summer, as water temperature increases, phytoplankton blooms are common.  This
algal  bloom  causes the  surface  of the  lake to  look  as if  green  paint were
floating on  it.  In  the  summer of 1973,  a Microcystis  bloom caused the drink-
ing water to  smell unpleasant and also  killed  many fish.

CONSERVATION MEASURES

     The Japanese  government  and the  prefectural authority are  improving the
water  quality of  the  Kasumigaura basin.  They  are trying  to restore  it  to
conditions prevailing in 1965 and to set a standard for research and implemen-
tation of this type of project.

     General  techniques  for conservation of water quality are:

     (1)  Removal of pollutants at the source by regulating drainage.

     (2)  Removal  of  pollutants  from  the  river which feeds  the  lake  by con-
          structing a treatment pond.

     (3)  Removal of pollutants from the lake by dredging  polluted sediments.

     (4)  Dilution of the polluted water with clean water.

The best technique or combination of techniques depends on the particular lake
or marsh.

     At Kasumigaura the following operations are planned or underway:

     (1)  Establishment of  sewage and storm drainage.

     (2)  Disposal  of livestock wastewater.

     (3)  Regulation of  industrial drainage.

     (4)  Dredging of polluted  sediments from feeder rivers.

     (5)  Dredging of polluted  sediments from Lake Kasumigaura.

     (6)  Removal of Microcystis aeruginosa.

     (7)  Introduction of clean water to dilute the polluted water.

     (8)  Cleanup  of Lake Kasumigaura  by  the  inhabitants   of  the  coastal
          cities, towns  and villages.

               DREDGING POLLUTED SEDIMENTS FROM LAKE KASUMIGAURA

     Drainage from residential,-industrial,  and agricultural activities is the
source  of impurities  found  in  the  water   of  Lake Kasumigaura.   The bottom
sediment of  the lake itself also releases impurities to  the water.  Therefore,
dredging has  been  done  since  1975 as  a  water  quality  improvement measure and
is included in the overall project for  cleaning  up the river.

                                       18

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     To eliminate the  sediment as a pollution source to Lake Kasumigaura, 1.2
x 106 m3  of  sediment must be  dredged.  About 3.0 x 105 m3 of the total are to
be dredged by 1981 as part of the project for controlling the water sources of
the  Kasumigaura.   This  project  in  turn is  part  of the  General  Development
Project for Kasumigaura.

     A  special  pneumatic  pump cutterless  suction  dredge, the  "Kasumi",  was
developed  for exclusive  use on  this project.  It is designed to prevent excess
turbidity  and  secondary pollution.   The "Kasumi"  and  another dredge  of the
improved  type, the  "Koryu",  have been dredging offshore from the mouth of the
Sakura  River  at  Tsuchiura  City  (Figure  5).   About 4,000 m3  were  dredged in
1975, 18,000 m3  in  1976, and  13,000 m3  in  1977.  The depth is between 1.4 and
5.7  m  after  dredging  and  the  thickness  of the cut is 0.5 m  on  the average.
The  water  content averages 260% and ranges  from  140%  to 400%.  Water content
was computed  according to the formula:

                                   w = Ww
                                       Ws
where:   w  = water content,  dry wt. basis
        Ww =  weight  of water
        Ws =  weight  of solids

The  dredged  mud  was  pumped by  pipeline to  the  disposal  area two kilometers
distant from the dredge, except in 1975 when the mud was transported by barge.
The  disposal  area will  become a park belonging  to Tsuchiura  City.   When the
mud  at  the disposal  area  is dry, is will be covered with soil and the facili-
ties for the park will be constructed.

THE TWO DREDGES

The  ''Kasumi", a  Sludge  Dredge with Pot  Type Suction Head and Pneumatic Pump,
6_0 m3/H Negative Pressure Suction and Positive Pressure Discharge.

     In 1971  the Sectional  Committee for Studying the Development of New Types
of  Machinery  and Methods  of Reclamation began meeting.   It  was  part of the
Engineering  Management   Conference  sponsored  by  the Bureau  of  Construction,
Kanto District.

     To establish a method for dredging the bottom while minimizing the resus-
pension  of  sediment,   the dredge  "Kasumi"  was  constructed.   The  following
conditions were used to develop the dredge:

     (1)  The dredge  should operate  with a  higher  percentage of  mud content
          than a  hydraulic  dredge.

     (2)  The turbidity caused  by dredging should be  curtailed  as  much as
          possible.

     (3)  The dredging cost should be less than the current costs.

These  conditions  for  development  led  to  the  utilization of the  "air-lift"
(pneumatic) system  developed  in  Italy.   The method employs  cylindrical  pump
bodies  pushed  into   the  bottom sediment.   Modification  of the pneuma system

                                      19

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employs a vacuum  inside  the pump body to suck bottom sediment in.  Compressed
air  is  then  forced into the pump  body  to push the mud  out  (Figure 6).   This
dredge was  constructed with the same specifications  as the 200  ps  class of
pump  dredge  regarding  draft,  clearance  and  beam  so  that  the  clearance of
bridges and  the span  of  bridge piers will  pose no problem when  it  is  being
transported.   A plan of the sludge dredge is shown in Figure 7 and the speci-
fications are given in Table 2.


            TABLE 2.  MAIN SPECIFICATIONS OF SLUDGE DREDGE "KASUMI"
Type:  Pot type suction head.  Negative Pressure Suction and Positive Pressure
       Discharge
Capacity:   60 m3/H
Maximum Discharge Distance:  30 m
Maximum Depth of Dredging:  5 m
Dimensions of the Hull:  60mx5mx0.9m (Length x Beam x Draft)
Weight:   78 Tons
Engine:  Water-Cooled Type, 4 Cycles, Diesel Engine.
Output Horsepower:  220 PS
Generator:  Waterproof, Self-Cool ing, with Self-Excited Generator.
Output Power:  Continuous Duty 180 KVA
Voltage:   440 V
     The  pontoons  which  provide flotation  also  house the  generator,  vacuum
pump,  air  compressor and  winch.   The boom with  the  mud-sucking equipment is
installed  at  the front of the dredge.   A vacuum pump  and  air compressor are
both used  for  dredging.   The inside of the  suction  head  is alternately pres-
surized  and depressurized.   An  automatic  valve  causes  the  sediment to  be
sucked up  and  sent  down the discharge pipe.  The swing wires at the front and
the  anchor  wires  at  the rear  are  used  to move the suction head and are oper-
ated by a winch on the pontoon.  Two suction heads are used to provide contin-
uous  cycle dredging.   The  volume  of one  cycle  is  0.5  m3 and  the duration
averages 60 seconds.  Thus the dredging volume per hour is estimated at 60 m3.
The  ship  is  designed with a maximum height of less than 2 m to clear overhead
obstructions such as  piers  and bridges.

     The  discharge  distance is  only 30  m.   This is because  the  mud is  dis-
charged onto  a barge where the  surface  water drains  into  the  river so  that
only the mud is transported to the disposal area.

     The  sediment  near  cities  and  towns  is  denser  because the  surface  is
covered at  high  water  and uncovered at low  water.   This  dredge was developed
and  manufactured  to  be  used  under  these  conditions.   Its   use in  Lake
Kasumigaura area required  little alteration.   Special  features are:

     (1)  Pot type.   Mud suction head with  pneumatic pump.


                                      21

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     (2)  Ability to dredge without causing turbidity.

     (3)  Disposal of water in the river instead of at the disposal area.               ^

The results of the performance test are shown  in Table 3.

The "Koryu", a  Sludge Dredge with Swing Type  Suction  Head and Pneumatic Pump
100 m3/H Negative  Pressure Suction and Positive  Pressure Discharge.

     Dredging has  been done  in  the  Lake Kasumigaura  region  since 1975.  The
dredge "Kasumi" worked  from  1975 to  1977.   The volume dredged had been esti-
mated at  1.2 x  106 m3.  About 3.0 x 105 m3 of this was to be dredged by 1982,
in accordance with  the project plan regulated by the Special  Law for Securing
Water Sources.   The  dredge "Kasumi"  had too small a capacity to fulfill this
project  and it  could  not  dredge the  lake  bottom smooth;  it left the bottom
wavy.   Therefore it was necessary to build another dredge.

     When  a sludge  dredge is  constructed today,  environmental  factors weigh
heavily.  A  dredge  of large capacity would  not be favored over  one  of small
capacity  which  caused less  secondary  pollution.   The  requirements  for  an
environmentally sound dredge  are that it dredge the lake  bottom flat, that the
suction  head or swing does  not generate excess  turbidity,  that the discharge
has a  high mud content  and  that  it  be capable of discharging  the  mud for a
long distance through a  pipeline.   Two kinds of suction  heads lend themselves
to this  kind of work.  One  is the pot  type,  the other the swing type (Figure
8).  The  "Kasumi" was a pot type.  It was decided to build the new dredge as a
swing type.

     This office  built  the sludge dredge "Koryu" in 1977.  It was paid for by      •
the  budget of  the  Construction Machinery  Arrangement  Expenses.  It  was  de-
signed as  both  an experimental  and operational machine.          ,  The basic
structure  of  the  dredge "Kasumi", built  in  1971,  was  adopted  for  use on the
"Koryu".  The new dredge was  equipped with a swing type pneumatic pump suction
head instead of  the pot type.

     The  dredge was completed in March,  1978,  and is  shown  in  Figure 9 with
specifications  given  in  Table  4.   Following  are  the improvements  over the
"Kasumi" design:

     (1)  Mud suction mouth of the swing pneumatic pump type.

     (2)  Mud collection equipment  which  does not generate turbidity.   It has
          a drag suction head with grating.

     (3)  Sonic thickness monitoring equipment.

     (4)  Spuds, anchors and wires used to move the  dredge.

     (5)  Long discharge distance.

     (6)  No overall turbidity.

     (7)  No disposal of effluents.

                                      24                                            I

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                                                               1.00
                            MAXIMUM
                            DREDGING
                            DEPTH
                      \   7.00
                                                              VACUUM
                                                              PUMP
      2.4^0
      2.4oC
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            Figure 9.  The sludge  dredge "Koryu."
                                 28

-------
            TABLE 4.  MAIN SPECIFICATIONS OF SLUDGE DREDGE "KORYU"
Type:  Swing Type Suction Head.  Negative Pressure Sediment Suction and Posi-
       tive Pressure Discharge
Capacity:  100 m3/h (Water Content = 66%)
Maximum Discharging Distance:  2000 m
Maximum Dredging Depth:  7 m
Dimension of Hull:   Length 25 m x Breadth 8 m x Depth 2.4 m x Draft 1.3m
Weight:  260 Tons
Engine:  Water Cooled, 4 Cycle, Diesel
Output Horsepower:   430 PS x 2
Generator:  Waterproof, Self-Cooling, with Self-Exciting Generating Equipment
Output Power:  Continuous Duty 350 KVA
Voltage:  440 V
     To swing the dredge head an hydraulic winch winds anchor-fixed wire ropes
through a  sheave  which is installed at the end of the dredging ladder.  Spuds
are  put  into the ground  alternately  to  move the dredge while  it is working.
With the  "Kasumi,"  the  mud  was  sent  to a  dumping  barge  or  discharged by a
booster pump.  In the  new dredge, the sludge is first stirred in a stock tank
installed  in the dredge to change the viscosity.  It is then sent to a second-
ary  hopper.  The  dust  is  removed by a vibrating  screen  installed in the sec-
ondary hopper.   The sediment  is  stirred again  and  discharged by  pump.  The
volume of the flowing sediment can be controlled by a valve on the bypass pipe
between the  pump  and  the secondary hopper.  Sonic thickness monitoring equip-
ment is  installed  to  check  how much bottom  sediment  is  dredged.  Because of
local  conditions,  the maximum  height of the  dredge while  operating is less
than 3.3  m.   This  dredge  is appropriate for work at  Kasumigaura because the
water content of the shallow sediments is  high.

     The  results  of  a short  field  performance  test are  given  in  Table  5.
Although future actual daily operations will probably yield different results,
it is clear that the designed nominal working capacity of 100 cubic meters per
hour at  66% water  content  will  be  met.   This also meets  the  planned annual
dredging volume required  by  the program.   From now  on both dredges, "Kasumi"
and "Koryu",  will  be used to dredge the bottom of Lake Kasumigaura.

                            SEDIMENT DISPOSAL STUDY

     About 1.2 million m3 of bottom sediment must be dredged by 1985.  In Lake
Kasumigaura,  the  sediments total  40-50  million cubic meters, according to rod
surveys conducted   at  35  points  in  the  lake.  The  average thickness  of the
sediment is  about 20  cm.   These sediments had values of 11-27% ignition loss,
indicating the  presence of  many organic substances.  Therefore, it  will  be
necessary to remove most of these sediments.  It will be  impossible to dispose
of this  large quantity of  dredged sediment  unless  we make use  of  a special
feature of the district.  Although it's  located on the fringe of the metropol-
itan area, 80% of the  land (2200 km2) is agricultural  and the sediment can be
disposed of on the farm lands.

                                      29

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             TABLE 5.   PERFORMANCE CAPACITY,  SLUDGE DREDGE "KORYU"

No.
1
2
3
4
5
6
7
8
9

Discharge
Volume (rnVhr)
128
110
107
106
108
102
101
97
101
97 - 128
Water
Content (%)









200 - 300%

     Tsuchiura City  (population  100,000)  and Ishioka City (population 40,000)
are located along  the  Jooban Line of the Japan National  Railway at the north-
western  part  of  the  lake.   The  Kashima Coastal  Industrial  Zone  is  located
downstream of the  rivers,  where  the existing  rice  fields  are to be reclaimed
for the city.

     Disposal  techniques are under study to use the sediments for rice produc-
tion and  landfill  for  the city.   Experiments are  being  conducted  to compare
rice growth  in  two  kinds  of soil,  one comprised  of sediment,  the other the
usual   soil.   Also  underway  are  experiments to dry the sediment naturally on
land surrounded by a soil  embankment where  the  dredged mud is deposited to a
thickness of  50-150  cm.  The water in the  mud  separates  as the sediment set-
tles and  consolidates.   The water is drained  and  then permeates underground.
The mud  left  behind  dries  in the sun.  Low water content  mud is used for this
purpose.  Following  is the  result  of a survey from February,  1977 to March,
1978.    The  accumulated  thickness of  mud  was  150 cm and the  initial  water
content  was   60-75%.    The   final   water content  was 54-60%.   The  complicated
influences of weather, water table, and evaporation from  the leaves of planted
vegetation  on the  process  of  settling  and consolidation  will be  studied.
Officials plan  to investigate ways  to shorten  the disposal  period  by using
supplementary solidification chemicals.

    REFERENCES (titles are in English, the document is printed in Japanese)

Matsubara, Mineo.   Reports  from the Working Site.  Kasen Review No. 22.

Kinoshita,  Ken  and  Tetsuo  Kaai.   Development of  Sludge  Dredger of Pneumatic
     Pump Type.  Kensetsu No Kikaika  July  1978.
                                      30

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                  LAKE SUWA WATER POLLUTION CONTROL PROJECTS

                          Akira Sakakibara, Director
                Qsamu Hayashi,  Chief,  River Development Section
   Civil Engineering Management Office for Lake Suwa and Surrounding Region
           Nagano Prefecture Department of Civil  Engineering,  Japan


                                 INTRODUCTION

     More than  a decade has passed  since water pollution  in  Lake  Suwa  first
attracted public attention.  During this  time,  eutrophication of the lake has
continued with no significant improvement  in water quality.  Algae continue to
bloom from summer to fall every year.

     In view of  the  seriousness of the problem, concerned public and private
interests are intensifying their studies to develop drastic measures to purify
the  lake  water.  This  is  the  tenth  year of dredging.   Partial  use of  the
basin-wide  sewage  system  will   start  next year.   This paper  outlines  their
efforts and  other  research  and projects  which  are one part of  the  slow but
steady progress being  made to improve the water quality of Lake Suwa.

     The water pollution control  measures being taken  in  Japanese  rivers  and
lakes  were  outlined  last  year  at the Third  U.S.-Japan  Experts'  Meeting on
"Management of  Bottom Sediments Containing Toxic  Substances"  (1).   In Kato's
paper  (1)  the dredging  of bottom  sludge at Lake  Suwa,  considered  the  most
polluted lake  in the  country,  is used  to illustrate  lake clean-up efforts in
Japan.

                   BRIEF DESCRIPTION OF THE LAKE SUWA BASIN

     Lake Suwa is located in the center of Nagano Prefecture at what is called
the "roof" of  the  Japanese Archipelago.  There are 31 rivers flowing into it,
but only the Tenryu river flows out.  The drainage area is 531 km2, the height
above  sea  level, 759 m, the planned  lake area, 13.3  km2,  the circumference,
16.2 km, the maximum depth, 6.8 m, and the average depth, 4.0 m.  It is also a
major recreational  fishery and water resource.

     The four  cities  of  Okaya,  Suwa,  Shimosuwa and Chino are on the periphery
of the  lake.  These cities (combined population about 170,000) form an import-
ant industrial area producing  optical  and precision machinery  and  food  prod-
ucts.   In recent years,  the modernization of lifestyles and expanding industry
have  led  to water  pollution  in  the  lake.  The  eutrophication of  Lake  Suwa
currently has reached its peak, with "Aoko" (Microcystis) growing in profusion
in the  summer, rapidly covering the lake  like a green carpet.   To make matters
worse,  Aoko creates an  offensive odor as  it dies and decomposes.  The concom-


                                      31

-------
itant "Susumizu  phenomenon"  (oxygen depletion)  adversely affects  the lake's
fishery.   These factors contribute  to  the  decreasing use of shoreline facili-
ties by tourists and local residents.

     Today, the dredging of the polluted sediments and the construction of the
basin-w.ide  Lake  Suwa  sewage  system  and related  public sewage  networks  are
being carried out to improve the environment of the four peripheral  cities and
prevent  future contamination  of the lake.

                         WATER POLLUTION OF LAKE SUWA

     The periphery of  Lake  Suwa has been rapidly  developing  as  an  industrial
area and  tourist resort.  The  pollution of  the  lake is a by-product of the
regional  development.

     Lake Suwa has long been known as a lake with extensive eutrophication but
recent levels have been extreme.  The inadequate sewage system around the lake
is a significant  cause  of pollution, but the  sludge  which has accumulated on
the  bottom for  a long time  is also  a  contributing  factor.   The  dominating
impact of  the  contamination,  from whatever source, is  the  nuisance growth of
Aoko and  clouds of mud in the  water.

EXTERNAL FACTORS

     The rivers and waterways  flowing  into Lake Suwa carry wastes from indus-
try, homes, agriculture  and  hot springs.  These loads create  a  BOD amounting
to 14,000 kg per day (Table 1).

            TABLE 1.   EXOGENOUS BOD LOADS PER DAY (1972), LAKE SUWA


             Classification                            BOD

          Industrial  waste                          10,634 kg
          Domestic sewage                            3,395 kg
          Livestock excretions                         209 kg
          Raw sewage                                   137 kg
          Agricultural  waste
          Total                                     14,375 kg
The  advanced  stage of  eutrophication  in the lake  is  attributed  to nutrients
such as nitrogen  and phosphorus, which flow in via the river (Table  2).

INTERNAL FACTORS

     Nitrogen and  phosphorus  input  to  the lake and,  accompanied  by high BOD,
cause  an  abnormally  fast growth of plankton and aquatic plants.  These organ-
isms in  turn  provide  sources of nitrogen  and phosphorus  for other organisms,
or die  and  become  bottom sediments.   The contamination of  the  lake is accel-
erated by this cyclic pattern.
                                      32

-------
                TABLE 2.  SOURCES OF NUTRIENT INPUT, LAKE SUWA
          Total
                                                      Inflow
                                          N load
3,327.3  (100)
 (kg/day) (%)
                              P load
Human wastes
Septic tanks
Sewage disposal facilities
Industrial wastes
Agricultural fertilizers
Mountains and forests
Fishery (feed)
Livestock wastes
Hot spring wastes
Gas well wastes
Rainwater
420
310
546
363.
754
247.
99.
55.
41.
463.
25.



8

3
8
6
3
9
7
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( 9.
(16.
(10.
(22.
( 7.
( 3.
( 1.
( 1.
(13.
( 0.
6)
3)
4)
9)
7)
4)
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7)
2)
9)
9)
116
21
47
53
85
4.
8.
24.
5.
7.
0.





2
5
6
3
5
68
(31.
( 5.
(12.
(14.
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( 2.
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1)
6)
6)
2)
8)
1)
3)
6)
4)
0)
2)
372.7   (100)
 (kg/day) (%)
Note:     The calculation of the above table is based on a run-off coefficient
               of 70%.  The pollution unit employed is borrowed from the 1970
               survey of the Ministry of Construction (Example:  Human wastes
               N = 3.0 g/man-day, P = 0.83 g/man-day).
QUALITATIVE CHANGE IN WATER QUALITY

     Studies of  Lake Suwa have been conducted  by  various  investigators since
1910.  These  provide some data  on the  historical  changes  in  water quality.
Because  of  differences  in  sampling and  testing  methods they  may  not  be di-
rectly  comparable,  but  they  show trends  of  change to  the  present  state.
Figure 1  shows  the location  of sampling  sites  in  Lake Suwa.  Figure 2 repre-
sents  the qualitative  change  in  the  lake's water quality  based  on such past
data.  Figure 3 shows the change in COD value in the center of the lake during
the  past  six  years.   Figure  4 shows the water quality from April  to December,
1977.  The extremely high COD and SS values in July through September indicate
the  vigorous growth  of Aoko  (Microcystis).   Line "A"  shows  the COD values of
the  lake water when filtered through filter paper (equivalent to JIS Class 5C:
0.45 p  pore size).  The COD values  are almost as  low as  the environmental
standard  of 3  ppm.   This demonstrates that the water quality can be drastic-
ally improved  by  removal  of the suspended matter, including Microystis.

     Figure 5 shows the  1976 investigation of the influences of Aoko and other
phytoplankton on the water quality at four points in  the lake.  In the figure,
"upper layer"  refers  to a position 0.5 m below the surface, and "lower layer"
1.0  m  above the  bottom.  The figure shows that the  average COD values of the
water after filtering  out the Aoko are  very  close  to the environmental stan-
dard.  These data  were  collected  in 1976 by the Suwa Health Center in accord-
                                                (text continues on page  41)

                                      33

-------
                                SHIMOSUWA
              LAKE   SUWA
1.    Center of Lake Suwa
2.    200 m offshore of the mouth of the Miyagawa river
3.    West of Hatsushima Island
4.    200 m offshore of the mouth of Osawa river
5.    200 m offshore of the mouth of the Tsukama river
6.    200 m offshore of the mouth of the Obori  river
         Figure 1.  Sampling sites in Lake Suwa.
                          34

-------
 ppm
   10
 8


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 4


 2


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o>
  O
  Q.
      Dr.
      Tan oka
        1910
                  Transparency (winter)
                          Transparency (summer)
Industrial
Research
Institute
      Dr.
      Kobayashi
  Nagano Research
  Institute for Health
  and Pollution
        Dr.
        Yoshimura
                                        M
                                        2.5


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'50
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                                                      '70
Figure  2.   Qualitative change  in water  quality of  Lake Suwa  (2)


                                 35

-------
in
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                                    I
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                                                           o

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                                                               ro
in         g

(uudd  )
      CM

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                                                               c:
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                                 36

-------
ss
ppm
40--20
30-
20 — 10
 IO--5
COD
ppm
 15
 o-^-o
Woter quality at center of Lake Suwa
                 April - December,1977
            i    i   i    I    i    i    i    i    r
    -COD
         SSyx
                  Environmental limit level

                   i    i    i    i    i
DO  i
ppm
PH
ppm
                                           20--10
                                       I5--9
                                            10--8
                                       5--7
       4   5   6   7   8   9   10   I
                    MONTH
                                          12
 Note: @ represents the COD values of filtered lake water
         (Number 5C filter paper).
                        Figure 4.
                           37

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    200m offshore of mouth of 1he Miyagawa River
                               Average COD:  6.3 ppm
                               Average COD of filtered
                                  water: 3.1 ppm
                                    Upper layer
                                    Lower layer
                                    Environmental standard
                                    Upper layer (filtered)
                                    Lower layer (filtered)
  JUN     AUG    OCT

Center of Lake  Suwa
                                 DEC
 20
  15
  fO

COD
ppm

   5
  0
        T
             T
                              Average COD: 7.6ppm

                              Average COD of filtered
                                  water:  3.0 ppm
                               Upper layer
                               Lower layer
                               Environmental standard
                               Lower layer (filtered)
                               Upper layer (filtered)
JUN
           AUG
                        OCT
DEC
        Figure 5.  Effects of phytoplankton on lake water.
                              38

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     200m offshore from the mouth of the Osowa River
  30
  25
  20
  15

COD
ppm

  10
   0
           Average COD:  11.2 ppm

           Average COD of filtered
              water-.  3.5 ppm
         I
_L
                                   Upper layer
                                   Lower layer
                            ->.0b.0.—Environmental standard
                               ^""^ Upper layerlfiltered)
                                  Lower layer (filtered)
        JUN    AUG
       OCT
DEC
                          Figure 5.
                            39

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West of Hotsushimo Island
                        Average COD:  10.9 ppm

                        Average COD of filtered
                            water:  3.3 ppm
                     I
                              Upper layer
                              Lower layer
                              Environmental standard
                              Upper layer (filtered)
                              Lower layer (filtered)
   JUN     AUG
OCT    DEC

  Figure 5.
                        40

-------
ance with the  lake  water measurement plan, 6-12/76.  Filtering was  done  with
0.45 u  filter paper.

     Figure 6 shows the results of water analysis at the center of the lake in
an undredged area and at the west of Hatsushima Island where dredging has  been
carried out.  These  results  show that dredging has  little  effect  in lowering
the  DO  value.   Data in  Figure  6 were taken from measurements  of  local  water
for  public  use  (Pollution  Section,  Nagano  Prefecture Department  of  Living
Environment).

BOTTOM MATERIAL

     Lake Suwa was  divided into 13 1-km square grids.  The bottom material in
each of the  13 grids was  analyzed in 1976 and 1977.  Figure 7 shows the aver-
age results of  the analyses.

     Currently,  there  seems  to be  no  explicit  standard  for the  removal  of
organic  sludge.   However,  elsewhere  in the  country,  the  following criteria
have been used:

               Ignition loss            15% or more
               COD                      20 mg/g or more
               Sulfides                 1.0 mg/g or more

     The above criteria  can be used to conclude that there are about 60 cm of
bottom sediment in Lake Suwa.

QUALITATIVE CHANGES IN ALGAL  GROWTH

     The most obvious impact of the eutrophication of Lake Suwa is the rampant
growth of algae.  The pollution of the lake may be characterized by the propa-
gation of Aoko  (Microcystis)  during the summer time.

     Diatoms (Diatomaceae) which generally grow  in  less  eutrophic  lakes  were
reported in  1918.   By  1948 diatoms had increased in  kinds and green algae and
blue-green  algae  (Cyanophyta) were  also  found.   In  the  1960s the  growth of
Aoko began to attract attention.  In the 1970s, its growth increased in inten-
sity.

                     WATER POLLUTION CONTROL IN LAKE SUWA

     The  Lake  Suwa Pollution  Control  Measures  Investigation Committee  was
established in 1965 to  study the lake's pollution and  immediately took action
to  control  and eliminate  the pollution.   The committee  conducted investiga-
tions for two years  and reported its conclusions  in  1968.  To control external
sources of  pollution it  recommended  the  construction  of the  Lake  Suwa Basin
sewage treatment  system  to eliminate the influx of polluted water (Figure 8).
To  control  the endogeneous  sources  the Committee  suggested  dredging the or-
ganic sludge deposited on the bottom.
                                      41

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 UNIT
                567
                  MONTH (1974)
                   8   9  10   II   12
            2   3  Ave.
  ppm
     25
     20
     15
     10
      5
  	0
COD
            ป    i    i    i    i    i    I    I
  •UNDREDGED AREA
      West of Hotsushimo
      Island (dredged area)
                           	DREDGED AREA
Center of lake
(undredged area)
  ppm
     15
      10
           Center of lake
            (upper layer)
                      West of Hatsushima Island
                      (upper layer)
         - West of H. Is.
          (lower layer)
            H—I—>
                            Center of lake
                            (lower layer)
                       H	1	1	1	1	r-
  ppm
     25
     20
      15
      10
      5
      •0
SS
  West of H. Is.     /
  (dredged area)  /
j_   i     i   i
 ^   Center  x.
 of lake (un- \
l dredged area))
                                   i	i
                j	i
Figure 6.  Results of water analysis  at center of lake in an undredged area.
                                42

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    o
    DO
        0.0
        0.3
        0.6
         0.9
         1.2
 COD       0
 SULFIDE  0
 IGN. LOSS  13
 T-N       2
                        I
 10
0.5
 14
 3
               • ---- Hi  T-N
               A - A  IGNITION LOSS
               p ------ -Q  SULFIDES
                      • COD
 I
                         I
20
1.0
15
4
30
 1.5
 16
 5
 mg/g
 mg/g
Percent
 mg/g
Figure 7. Average results of bottom sediment analysis in 1976 and 1977,
                              43

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LAKE SUWA BASIN SEWAGE SYSTEM CONSTRUCTION PROJECT

     A major cause  of  pollution in Lake Suwa was  raw sewage,  so construction
of a large-scale sewage and treatment system was a fundamental step.

     The  construction  project began  in  1971 and  will  be  completed  in  1992.
Tables 3, 4, and 5 provide statistical  data  on the project.

                TABLE 3.   LAKE SUWA REGIONAL SEWAGE SYSTEM PLAN

District
Okay a
Suwa
Chi no
Drainage
Area
(ha)
1,508
1,423
715
Shimosuwa 516
Total
Table 3
Sewer
System


Sepa-
rate
System

4,162
(cont. )
Treatment
Plant
(GA ha)


Toyota
Sewage
Treatment
Plant
18.7
Future Total
Population Distance
(Est. 1,000) (km)


1985: 200
1990: 212


Pumping
Station
(GA m2)


Shimo-
suwa
Sewage
Pumping
Station
1,320
Koshu TS
(Trunk Sewer)
Chi no TS

Chuoh TS
Nishiyama TS
25.6

Construction
Period
(FY)


1971 - 1985

Sewage
Volume Treatment
(1 ,000 nrVday) Process

Ordinary
Activated
1985: 334 Sludge
Process
1990: 337


Administrative
Authority Authorization
Authorized by
Prefecture
Dec. 27, 1971
Nagano Authorized by
Prefec- City Planning
ture Law
March 24, 1972
Authorized by
Sewage Law
Feb. 28, 1972

GA = ground area
FY = Fiscal  year
(continued)

-------
Table 3 (cont.)
                       Estimated Sewage Volume (m3/day)

Average
Per
Item Day
Sanitary -,,. ~0-,
r J 76,337
Sewage '
Industrie!
Hot
Spring 17,257
Waste
Ground ?3 •,„(-
Water '
rtrVday 337,099
m3/hour 14,000
Tnt ->1
m3/sec 3.9
Maximum
Per
Day
95,425
220,310
21,571
23,395
360,401
15,000
4.2
Maximum
Per
Hour
143,140
330,468
32,357
23,395
528,954
22,000
6.1

Outline of Sewage
System


Item
Koshu
Trunk Chinฐ
Sewer Chuoh
Nishiyama
Sewage Pumping
Station
Sewage Treatement
Plant
Discharge #1
Trunk #2
Pipe
Diameter
(6 m)
0.9 - 2.4
0.7 - 1.2
0.8 - 1.4
0.4 - 1.4
2 Stations
(Toyota &
1 Plant
(Toyota)
1.5 - 4.5
0.8
Distance
(km)
11.6
6.8
6.2
1.4
Shimosuwa)

4.7
4.3
                                      46

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     The construction progress is shown in the following tables.   Partial use
of the system is expected by October, 1979.

                 TABLE 4.  CONSTRUCTION PROGRESS OF LAKE SUWA
                           BASIN SEWAGE SYSTEM (MILLION YEN)
 Item
    Total
Construction
1971  - 1978
 Remaining
Construction
               TABLE 5.  CONSTRUCTION PROGRESS OF COMPLEMENTARY
                         PUBLIC SEWAGE NETWORKS (1973-1978)
                                                                     Progress
Trunk sewer
Discharge trunk
Toyota sewage
treatment plant
Shimosuwa sewage
pumping station
Subcontracting;
wages, etc.
Total
12,789
4,952
40,251
1,023
2,985
62,000
6,664
448
7,993
713
2,212
18,030
6,125
4,504
32,258
310
773
43,970
52.1
9.0
19.9
69.7
74.1
29.1


City
Okay a
Suwa
Chino
Shimosuwa
Total
Constructed
area (ha)
46.3
108
37
26.8
218.1
Distance
(m)
10,525
19,685
6,634
4,772
41,618
Cost
(million yen)
1,030
1,743
467
466
3,706
Total
area (ha)
1,507.8
1,423.4
714.7
515.6
4,161.5
Progress
(%)
3.1
6.2
5.2
5.2
5.2

EFFLUENT CONTROL OVER  INDUSTRY

     Since completion  of  the  sewage system is still several years away, local
governments  enacted  ordinances   setting  their  own environmental  standards.
These drainage  standards  required designated business firms in the basin area
to  meet the  nation's  environmental  standard  for  lakes  and  marshes.   Such
standards are applicable  to  factories  and offices  whose  average  drainage per
day  exceeds  30  m3.    Local  health centers  are  assigned to  conduct on-site
inspections to  insure  compliance.
                                     47

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DREDGING PROJECTS

     Lake  Suwa   is  a shallow  lake with  an  average  depth  less  than 4.0  m.
Deposited on the bottom is a thick sediment layer resulting from the inflow of
polluted water  into the lake over a  long period of time, and  organic  sludge
from dead  and decomposed  aquatic plants and plankton.   The adverse effects of
these bottom  sediments  on  the  water  quality  is quite evident,  particularly
when sedimentary mud  churned  up by high waves creates  water masses with  a low
oxygen content.  This "Susumizu phenomenon"  is doing extensive damage to the
lake fishery.  Dredging is  therefore  another  fundamental  step,  along with the
sewage system, towards regaining a clean lake.  Table  6 presents environmental
standards for lakes  and marshes.
  TABLE 6.   ENVIRONMENTAL STANDARDS FOR LAKES AND MARSHES (Natural  lakes and
            marshes and artificial  lakes of at least 10 million m3  capacity)
                                        Standard
                                                                       Water

AA


A


Quality
City water 1st
grade
Fishery 1st grade
Natural environment
and Classes A, B, C
City water 2nd, 3rd
grades
Fishery 2nd grade
Bathing and Classes
B, C
pH
6. 5 or
above
8.5 or
below

6.5 or
above
8.5 or
below
COD
1 ppm
or
below

3 ppm
or
below

SS
1 ppm
or
below

5 ppm
or
below

DO
7.5 ppm
or
above

7.5 ppm
or
above

Col i form
Count
50
MPN/100
ml or
below

1,000
MPN/100
ml or

Body

Lake Suwa*
Lake
Shirakaba*
Lake
Tateshina*
     Fishery 3rd grade
     Industrial water
       1st grade
     Agricultural water
       and Class C
6.5 or  5 ppm  15 ppm   5 ppm
above     or     or       or
8.5 or  below  below    above
below


C

Industrial water
2nd grade
Environmental
protection
6.0 or
above
8.5 or
below

8 ppm
or
below
No
sus-
pension
of dust

2 ppm
or
above

  entire lake
                                      48

-------
Basic Dredging  Concepts

     Basic concepts  to support the dredging efforts are based  on  the  following
results from  the studies  made  by the  Lake  Suwa  Pollution Control Measures
Investigation Committee:

     1)   Easily decomposed organic  matter is deposited on  shallow  areas near
          shore.

     2)   Higher aquatic plants do not proliferate  at water  depths of over 2.5
          m.

     3)   Dissolved  oxygen  (DO)  at a depth of 2.5 m  is higher than  at  lesser
          depths and almost equivalent to the DO at  greater depths.

Thus, dredging  at water depths of less than  2.5 m will  be most effective.

     Based on  this  conclusion  a  plan  was drafted to  build  a  new  shoreline
while retaining a substantial  lake area of 13.3 km2  for flood control (Figure
9).   The old lake area was  14.06  km2.   The dredged  sludge  would  be  dumped in
the  area  between the new  and  old shorelines and  a greenbelt of streets and
parks would be created by covering  it with clean soil.
           TENRYU RfVER
    KAMAGUCHI FLOODGATE
         FLOOD CONTROL
            EMBANKMENT
        RECLAIMED AREA
          (EXAGGERATED)
          SHIMOSUWA
FIRST STAGE
DREDGING AREA
                                                       RUINS OF
                                                       SONE
                                                      SUWA
                                        KAMIGAWA
                                        RIVER
              Figure 9.   Dredging  and  diking plan for Lake Suwa.
                                     49

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Dredging Plan

     The dredging  at Lake  Suwa was  initiated  in 1969  as one  of the "river
environment protection  projects"  subsidized by the Japanese National Treasury
(50% subsidy).  The project is currently about 70 percent completed (Table 7).

                    TABLE 7.  FIRST STAGE OF DREDGING PLAN
    Item
Total Plan
1969 - 1977
Completion (%)
   Project
    cost
(million yen)
     2,466
     1,466
     63.7
Dredged
sludge 1,656,000 1,211,860
(m3)

73.2


     The planned  dredging area  is  about  2.5  km2 or about  18  percent of the
planned  lake  area of  13.3  km2.   About  78 percent of  the  dredged sludge was
used as fill material between the new and old shorelines and 22 percent as top
dressing to  cover fields.  This  activity has  been  implemented  with care to
avoid secondary pollution.
                                         13.5 m
          WATER LEVEL	759^45(1.1) ^
                'FOOT PROTECTION  -'P"-" I
                                                      'DREDGED OR FILL MATERIAL
                    Diagram of dredge and backfill of new shorelines.
Dredged Sludge
     The soil at the dredging area, typified by such characteristics  as  granu-
lar  variation,  hardness and  specific gravity,  affects  the dredging  ability.
The  results  of  soil  examinations are shown in Table 8; test sites are identi-
fied in Figure 10.
                                      50

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TABLE 8.  SOIL SAMPLE CHARACTERISTICS

Sample No.
Item
True specific
gravity
Liquid limit
Plastic limit
Gravel content %
Sand content %
Silt content %
Clay content %
Max. grain size
mm
Uni formity
coefficient Uc
Curvature
coefficient U'c
Soil type
PH
Ignition loss %
Remarks

10
2.517
NP
NP
0
5.2
80.3
14.5
0.84
10
-
silt
7.2
5.1
dark
brown,
offen-
sive
odor
11
2.615
NP
NP
0
27
59.5
13.5
0.84
17
-
Psam-
mitic
silt
5.8
11.5
dark
brown,
offen-
sive
odor
12
2.693
NP
NP
0
15.7
77.5
6.8
0.42
4
-
Psam-
mitic
silt
6.4
9.1
dark
brown

13
2.419
-
-
0
22
24
54
0.42
-
-
clay
-
-
dark
brown,
offen-
sive
odor
14
2.828
NP
NP
0
93
4
3
-
2.9
1.2
sand
-
-
dark
brown

15
2.627
NP
NP
0
12
76
12
-
8.8
1.6
Psam-
mitic
silt
-
-
dark
brown,
offen-
sive
odor
16
2.629
NP
NP
0
15
75
10
-
7.3
1.5
Psam-
mitic
silt
-
-
dark
brown,
offen-
sive
odor
                 51

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                               TOGAWA RIVER
       YOKOKAWA RIVER

                     16
  TENRYU RIVER
10
                            LAKE  SUWA
                          STOCKS OF
                          AQUATIC PLANTS
                                                     KAMIGAWA RIVER


                                                MIYAGAWA RIVER
       • soil sample (see Table  8)
       o core sample
                         Figure  10.  Test sites.
Dredging Methods
     For this project a pump dredge was selected from among the various types
of available  dredges.  This was done for  the following reasons:

     1)   Lake Suwa is a shallow inland lake.

     2)   There  are many fishing  facilities  and ferry  lines  operating within
         the lake.

     3)   Pump  dredging  can be  performed  with  a high mud content of  the
         dredged material  and  without  dispersing the  sedimentary mud in  the
         water.
                                  52

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     Pipeline  transportation of dredged material  avoids emission of offensive
odors.   The pipelines  were laid along the  lake  bottom  to  avoid obstructing
vessels.   Dredging equipment and pipeline specifications are shown in Tables 9
and 10 and Figure  11.
       DREDGE
 PUMPING METHOD TO SEND MUD THROUGH PIPELINE TO DUMPING AREA
                         Figure 11.  Pipeline system.
                        TABLE 9.   DREDGING EQUIPMENT
    Speci fi cations
Main dredge  (one)
Auxiliary  dredge
      (one)
                                    Relay boat  (one)
Total weight  (tons)

Type
Length (m)
Width (m)
Draft (m)
Main engine
Dredging depth  (m)
        96
        125
                                           65
Portable, on site  Portable, on site  Portable,  on site
fabrication        fabrication        fabrication
        18.0
         6.5
         1.0
  Electric motor
     (350 PS)
         4.0
         19.0
          7.0
          1.0
  Diesel  engine
    (420  PS)
          4.0
                                           15.0
                                            6.0
                                            0.8
                                      Diesel  engine
                                        (420  PS)
distance (m)
Pumped water (m3/h)
Total pump head (m)
900
70
45
900
70
45
600
70
45

Note:      Mean mud content up to  50%
          Sludge transport pressure 5 kg/cm2
                                    53

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                      TABLE 10.   PIPELINE SPECIFICATIONS
     Pipeline pressure during sludge transportation:   50 kg/cm2.
     Flow rate in pipe during sludge transportation:   3.025 m/sec.
     Diameter of sludge pipe:  310 mm
     Length of sludge pipes in water (synthetic rubber pipes):   12  m/pipe.
     Length of sludge pipes on land (cast iron pipes):   6 m/pipe.
     Based on  dredging results,  (Figure  12),  it is recommended that  a relay
boat be used where the transport distance is over 1,300 m.

     Dredged sludge contains polluted water;  when it is used as fill  it can be
a secondary source  of  pollution if allowed to return to the lake.   To prevent
this,  the  sludge is induced  to settle rapidly at  the  reclamation  area.   The
area between the  new and  old shorelines is  divided  by dikes into  small ponds
(average  length:   50  m, width:   30  m, depth:   1.8 m).  The sludge  is pumped
into these ponds  and the  water is removed.  From the  viewpoint of  sedimenta-
tion efficiency,  the  best  sludge transportation rate was 0.3  m/min  or less.
From the  standpoint of  an  efficient dredging project,  this  rate was too slow
and  could not  be  tolerated.   The relationship  between grain  size,  settling
time and depth  is shown in  Table 11.

                 TABLE  11.   APPROXIMATE SETTLING TIME (HOURS)
                          Settling depth
             Grain size                        1.0m       1.8m
1.0 u
0.7 u
3
4
3.6
4.8

     The local prefecture's  SS  criteria calls for 70 ppm.  The national stan-
dard  is  150 ppm  (Water  Pollution Prevention Act).   Natural  settling without
coagulant agents  produced 100 ppm SS  discharges.  Dredged  material  discharge
to  the  settling  ponds could  not  reasonably  be  reduced 0.3 m/min  in  order to
meet the return  flow  SS  criterion, therefore it was  necessary to use a coagu-
lant.  The SS value was  reduced to 50 ppm when  150 to 180 ppm of polyaluminum
chloride coagulant was used.

Remaining Problems

     About 10 years have  passed since the first stage of the Lake Suwa Dredg-
ing  Plan began in  1969.   The project will be about 80 percent completed by the
end  of  1979.  Even  with  the  completion of  the  first stage  in a  couple of
years,  no  noticeable  improvement of  the lake's  water quality  is  expected,
partly because the sewage system around the lake has not been completed.

                                       54

-------
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                                                                  CO
                                                                  — CO
                                                                  Q 2
                                                                      ^

                                                                  t- $
                                                                  cr s-
                                                                  o ?
                                                                   <
                                                              cv   f
                                                              ro
                                                                      Q
                                                                      CU
                                                                      i.
                                                                      ^
                                                                      CT:
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  CD
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O
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                         55

-------
     Every  summer  the  Aoko phytoplankton bloom that  symbolizes  the  pollution
of  Lake  Suwa turns the  entire  surface  of the lake green.  The  Susumizu  phe-
nomenon,  triggered by  bottom sludge,  still  occasionally occurs.  There  is,
however, a  promising aspect  to  the project which  requires  further investiga-
tion.   Up  until  1963,  the annual  harvest  of  prawns from the  lake averaged  8
tons.   By  1968  it was  reduced  to zero.   But since 1970, the second  year of
dredging work, the prawn catch has gradually increased to a  current level  of 3
tons per year.

     Even when dredging  is  completed  in all areas of  the lake less than 2.5 m
in  depth,  more  than 80  percent of the deposited  sludge will remain  in  the
lake.   It may still cause phytoplankton  blooms and is  therefore an obstacle to
the rehabilitation of the lake.

     Construction of the basin-wide sewage system (started  in 1971)  has  been
making steady progress  and  partial  use of the  system is expected  in October of
1979.   Its  effect on the lake  water will be known in a few years.

     Consideration is also being  given  to expanding dredging  to  areas deeper
than 2.5 m  (over  80%  of the total lake area).  Before a final decision can be
made it  will  be  necessary  to determine what the new sewage  system can do.   In
addition, a  study  is currently  being  conducted on  the  flux  of organic matter
and nutrients in the lake.

     What remains  is to  accurately measure the influence of  bottom  sludge on
water pollution.   A small  portion  of  this work has already  been  finished and
is reported in the following section.

     The biggest problem to  be  solved in  the  future  is  how and  where to  dis-
pose of  newly dredged  sludge,  since  the  fill  area  between  the new  and  old
shorelines has been almost completely filled.

                      OUTLINE OF BOTTOM  MATERIAL ANALYSIS

     In  1976  and  1977  a study was made  of the bottom sediments  of  Lake  Suwa
(Figure  13).  It  consisted of sediment analysis,  elutriate  testing,  examina-
tion of  mud  suspension in  the  water column,  and determination  of  sediment
thickness.    The  idea  was  to determine  the effects of  the  sediments  on  the
water and the minimum dredging depth required to clean up the  lake water.

LIST OF ANALYSES

     a.    Sediment analysis

          Sample:         4  depths per  station:  0, -30, -60,  -90  cm

                         Total samples:   52

          Analysis:      Water content as percent dry  weight,  simple  weight
                         per volume,  ignition  loss, total carbon,  total nitro-
                         gen, sulfide, COD.
                                      56

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     b.    Elutriate test

          Sample:         2 depths per station:   0,  -60 cm

                         Total  samples:   10

          Analysis period:     10 analyses per sample:

                              Day 1,  3,  6,  10,  15,  20, 30,  45,  and 60

          Analysis:       COD,  TOC,  total  nitrogen,  NH4-N, total  phoshporus,
                         P04-P,  DO

     c.    Analysis of mud suspension  in  the water column

          Sample:         2 depths per station (upper and lower  water layers)

                         Total  samples:   16

          Analysis:       SS,  water  content, specific gravity,  total phosphor-
                         us,  total  nitrogen, COD, N02-N, N03-N,  NH4-N,  P04-P.

     d.    Sludge thickness

          Device:         Model  RS-72  (Rasa Electronic Industries,  Ltd.)

          Frequency:      400  kHz, 30  kHz

          Total  distance traversed:      27.0 km

Results  of the investigation  are detailed in Tables 12 through  15.
              TABLE 12.   AVERAGE CONTENTS OF BOTTOM SEDIMENTS AT
                         DIFFERENT DEPTHS IN THE UNDREDGED AREA

Depth
- 0 cm
-30 cm
-60 cm
-90 cm
Water
content
(%)
473
349
282
180
Weight
(g/cm3)
1.14
1.17
1.27
1.37
Ignition
loss
(%)
16.3
16.4
14.7
13.5
TOC
(mg/g)
42.2
40.8
35.5
26.3
T-N
(mg/g)
4.49
4.00
3.41
2.73
Sulfide
(mg/g)
1.10
1.40
0.91
0.53
COD
(mg/g)
30.1
31.1
18.5
15.8
                                      58

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TABLE 13.   EFFECTS OF BOTTOM SEDIMENTS AT 0 cm AND -60 cm ON WATER
           QUALITY AS DETERMINED BY ELUTRIATE ANALYSIS AFTER 60
           DAYS WHEN THE SEDIMENTARY MUD IS CONSIDERED MOST STABLE

Sample
0 cm
sample
1
2
3
4
5
Average
COD
(mg/1)
- 1.
- 0.
0.
0.
1.
0.
0
4
2
2
1
0
TOC
(mg/1)
- 2.0
-
-
1.0
1.0
0.0
T-N
(mg/
- 0.
0.
0.
- 0.
- 0.
- 0.
NH4-N
1) (mg/1)
33
30
34
77
37
17
T-P
(mg/1)
0.
0.
0.
0.
0.
0.
10
06
06
01
07
06
P04-P
(mg/1)
0. 14
0.15
0.14
0.13
0.16
0.14
DO
(mg/1)
- 3.
- 2.
- 3.
- 4.
- 3.
- 3.
2
9
1
0
1
3

-60 cm
sample
1
2
3
4
5
Average
0.
0.
0.
1.
1.
0.
9
2
1
3
5
8
-
2.0
-
1.0
1.0
0.8
- 0.
- 1.
- 1.
— "1
- 2.
- 1.
85 - 0.05
30
70 - 0.28
14 - 1.26
42 - 2.36
48 - 0.79
0.
0.
0.
0.
0.
0.
07
08
07
10
10
08
0.16
0.16
0.16
0. 16
0. 16
0.16
- 1.
- 1.
- 1.
- 1.
- 1.
- 1.
5
3
0
0
1
2

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(0 cm
s) -
s)
0.
8
0.8
- 1.
31 - 0.79
0.
02
0.02
2.
1
                                59

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           TABLE 15.  EFFECTIVENESS OF DREDGING BASED ON THE RESULTS
                      OF THE CURRENT INVESTIGATION AND EXISTING DATA

Data
Item
Effective
depth
Effect
Current
Investi-
gation
           DO
           Sulfide
Ignition
  loss
           COD
           Suspended
             Mud

           Sludge
           Thickness
             -60 cm
            DO consumption reduced by 2 ppm
-60 to -90  Maximum at -30 cm.   Almost same value at
  cm          bottom surface and -60 cm.   Reduced dras-
              tically at -60 to -90 cm,  the value being
              below 1.0 mg/g at any point

-90 cm      No drastic reduction seen.   15% or below
              at -90 cm at most sites (11 out of 13
              stations).

-30 to -60  20 mg/g or below at -60 cm at all points.
  cm

-30 cm      Returns to bottom material  before "Susumizu
              phenomenon" occurs.

-20 to -60  Eliminate sludge layer
  cm
Existing   Methane
  data     Production
             -20 cm
            Reduced bottom surface production to 1/10.
RESULTS OF ANALYSIS

     1.   In the elutriate test, the materials at 0 cm and 60 cm in depth were
sampled  at  5 points.   About  150 g  of evenly mixed  mud was put  in  1-1  dark
bottles  with  700  ml  of filtered lake water  (5A  filter  paper).   Dark bottles
were also  filled  with  filtered lake  water  only as  controls.   Both  types of
bottles  were  sealed  and retained for  testing.  Water analyses  of  both bottle
types were made  on  each specified day.

     Lake water  sampled  for  the test  (on August  3rd  and 4th, 1977) contained
little NH4-N.  Most of the total nitrogen is considered to exist in an organic
state.   This may be  due  to nitrogen uptake by Aoko (Microcystis) in the upper
layers.

     About  80-100%   of   the   phosphorus  in  the  water  existed  in  P04-P.
Microcystis growing  rapidly  in  the  summer  quickly takes up  P04-P  as  well as
NH4-N.    The  fact that P04-P existed with  little NH4-N and N03-N  in  the  lake
water suggests that N is the  limiting factor in the propagation of phytoplank-
                                      61

-------
ton  in  the upper water  layer of the  lake,  at  least at the time  of  sampling
(Table 16).
             TABLE 16.   ANALYSIS OF RESULTS OF CONTROL BOTTLES OF
                        FILTERED LAKE WATER (5A filter paper)

C.O.D.
(mg/1)
3.0
T.O.C.
(mg/1)
8
T - N
(mg/1)
1.99
NH4-N
(mg/1)
0.01 or
above
T - P
(mg/1)
0. 19
P04-P
(mg/1)
0.19
DO
(mg/1)
7.2

     2.    The methodology used  in  the  mud tests was proposed by Dr.  Koyama of
Nagoya University  and  others.   Sampling  devices  were made  and used  for one
month.   Two of the  devices  sustained  damage from ferryboats.  At three of six
stations,  a  large  quantity  (15-8  cm)  of  particles with  specific  gravity
greater than 1.1  were suspended 1  to 2 m above the bottom.   At the other three
points the SS layer was much  less (less than 3 cm).

     The  1.0 to  2.0 m  thick suspended  solid  layers  contained  600 to 1000 ppm
of SS.  Once resuspended, this mud suspension does not settle easily.  Once in
suspension it can migrate to higher layers  or to the surface.

     The  thickness  of  bottom  sediments  contributing  to  the  dense  overlying
layers of suspended mud was calculated  from the data to be less than 1 cm.  In
the  lake it  would be  a  few centimeters  at  most.   Since  Lake Suwa  is  very
shallow  with  an  average  depth  of about  4 m  and  a maximum  depth of  6.8 m,
wind-blown waves  can easily reach the bottom and cause mud resuspension.

     3.    The results of  sludge thickness measurements showed that the sludge
in the dredged area was about  10 cm thick.  That of the  undredged area was 20
to 60 cm.

     4.    The bottom sediments of  Lake Suwa display very  small  unit weight and
grain size.  Consequently, dredging  to  a  depth of  -90 cm  may not effectively
prevent  mud resuspension.  But the Susumizu phenomenon caused by suspended mud
did  not  occur  before  1966.   The rate of sedimentation in Lake Suwa is 5 to 20
cm over  10 years.  Considering that the  sediment  thickness  which causes mud
resuspension  is  only a  few  centimeters,  we estimate about  30  cm  of dredging
will  restore the bottom to  1965 conditions, when the  Susumizu phenomenon did
not occur.

                                  CONCLUSION

     More than a decade has passed since water quality  control efforts began
in Lake  Suwa,  one  of the most  eutrophic  lakes in Japan.   During this period,
scientific  investigations  have  been   conducted  and  administrative  measures
taken.  But pollution continues and algal blooms occur yearly.
                                       62

-------
     However, the construction  of  the Lake Suwa Basin  Sewage  System  has made
steady progress since  its  beginning in 1971.   Partial  use  of  the  system will
begin in October, 1979.  Progress  is  also being made in the river  improvement
projects around the lake and in dredging of the lake itself.  But a method for
total  rehabilitation  of the  lake  has  not yet been  found.  Research  is  now
being done  to determine the  mechanisms of organic pollution  and  the methods
appropriate to predict the behavior of pollutants in the lake.

     It will  take  a long time, but all  the projects in Lake  Suwa  are making
progress toward  restoring the lake to cleaner,  purer water quality.

                                  REFERENCES

(1)  Lake  Suwa  Purification  Measures  Investigation  Committee,  "Studies  on
     Purification of Lake Suwa".

(2)  Nagano  Research  Institute  for Health and Pollution,  Pollution  Section,
     Nagano Prefecture Department of Living Environment, "Report on Investiga-
     tion of Countermeasures against Eutrophication of Lake Suwa".

(3)  The  Civil  Engineering Management  Office  for  Lake Suwa  and  Surrounding
     Region,  "Examination of  Lake's  Bottom Material  as Part of River  Environ-
     ment Improvement Works".

(4)  Nagano Prefecture,  "Pollution White Paper".
                                      63

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                     DREDGING OF POLLUTED BOTTOM SEDIMENTS
                               IN THE IBO RIVER
                                Sadao Kishimoto
                        Director of Himeji  Work Office
                      Kinki  Regional  Construction Bureau
                        Ministry of Construction, Japan
                                 INTRODUCTION

     Located in the western part of Hyogo Prefecture,  the Ibo River flows into
the Seto Inland  Sea  at Himeji City - about 80 kilometers west of the Interna-
tional  Port of  Kobe.   This  region  is located along the  Sanyo Route, histori-
cally an important connection between the western part  of  mainland Japan and
Kyushu Island,  Shikoku  Island and the Chugoku Region.

     Various industries  have  developed  in  the  basin,  notably  brewing,  the
production of Japanese  noodles,  and leather manufacturing.   The leather manu-
facturing factories  along  the Hayashida River,  a tributary  of  the lower main
channel  of  the Ibo, have  created  a  serious water pollution problem  in both
rivers.   This  has  also caused  a large volume of bottom sediments containing
polluted substances  to  accumulate on  the  river beds.   In the  dry  season,
unavoidable impacts  from this pollution  are found  in the  form  of foul  odors
and other negative  influences on irrigation, fishing and the general environ-
ment.   The volume of polluted bottom sediments is estimated  at 8,000 m3 at the
confluence  of  the  Ibo and  its tributary,  the  Hayashida   River.   The  total
volume,  including that  in  the river estuary, is  estimated  at several  tens of
thousands of cubic meters of sediment.

     To deal with  this problem, stricter  regulation  of  wastewater discharge,
the construction and improvement of sewage  treatment  facilities  and dredging
of bottom sediment are now being adopted.  This  paper describes  the plan for
dredging the bottom sediments.


                           THE OUTLINE OF THE BASIN

     The  Ibo   River  is  shown  in  Figure  1.   Its  headwaters   begin  at  Mt.
Fujinashi  (1,139 m)  in the  Chugoku mountain chain.   As  it  flows  to the Seto
Inland  Sea  it  is  joined  by  major tributaries  -  the Hikihara,  Kurusu,  and
Hayashida Rivers.  The area of the Ibo basin is  approximately 810 km2,  and the
length of the main river channel is  71  km.


                                      65

-------
                 CATEGORY A
       NEW SANYO LINE

        SANYO LINE
CONFLUENCE

ESTUARY-'.:'-
Figure 1.
The Ibo River Basin.

-------
     The major part of the basin is situated in mountainous terrain - the flat
area is only  170  km2,  about 20% of the total area.  Hayashida Watershed occu-
pies 97 km2 of the basin.

     The  geology  consists  of  basaltic  andesite  and  quartz  diorite  in  the
mountains and alluvial strata in the valley.  The total forest area of 640 km2
is composed of 190 km2 coniferous forest, 260 km2 deciduous forest and 190 km2
brush.

     Annual average  rainfall  in  the  basin  is  about  2100  mm upstream, about
1600 mm in the middle stream and about 1400 mm downstream.  The riverbed slope
is 1/2000 to 1/100 in the Ibo River  and 1/360 to 1/280 in the Hayashida.

     Table 1  shows the  18 year average  stream flow  at  Tatsuno  in  the main
river.   Table 2 shows the monthly mean flow at Tatsuno, Kamigawara (Ibo River)
and  Karnae (Hayashida  River)  for  1975  and  1976.   As  these  tables  indicate,
heavy flow is  expected in the rainy season,  and zero flow in the dry  season.

     The  watershed area  of the  Hayashida  River  is  affected by the climate of
the Seto  Inland  Sea.   Its discharge per unit drainage area is roughly 70% of
that of the main river.

     The  Ibo  River drainage  area  contains two cities and  eight towns, total
population about  200,000.  Downstream the Harima seaside  industrial  zone is
located,  an  area  of  extensive  chemical  and heavy  industries.   From Tatsuno
City  to  Himeji  City brewing,  noodle  and  leather  industries  are  dominant.
These  industries  are  major  sources  of  pollution,  particularly  the leather
industry.

     The present water rights in the Ibo River are 0.09 mVsec (0.2%) for city
water  use,  5.15  m3/sec  (15.9%)  for  industrial  water  supply,   16.98  mVsec
(52.4%) for agricultural  use  and 10.20 mVsec (31.5%) for power.  The maximum
volume  is 32.41 m3/sec.  The water withdrawn below the Hayashida River conflu-
ence is used for agricultural  and industrial purposes,  thus water quality is a
major concern.


   PRESENT CONDITION OF WATER QUALITY AND BOTTOM SEDIMENTS IN THE IBO RIVER

WATER QUALITY OF THE IBO RIVER

     In May 1973, the law which set environmental standards was applied to the
Ibo  River,  and the  stream above  the  Hayashida confluence  was  classified as
category  A and  the stream below as category  B,  (Figure  1, also Table 3 for A
and B).

     Since the  biological oxygen  demand  (BOD),  suspended  sediments (SS) and
dissolved oxygen  (DO)  values  in the middle  and  upstream  Ibo are respectively
1.0-1.5 mg/1,  13-19  mg/1  and  9.9-10.4 mg/1,  there  are few pollution problems
there.   Therefore  this  discussion  will  concentrate on the severely polluted
tributary, the Hayashida  River and its confluence with the main river.

     Three bottom  sediment monitoring  stations,  shown in Figure 2 were estab-
lished:   Tatsuno  station  in  the  Ibo  River, Kamae  station  in  the  Hayashida

                                      67

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-------
                                      TO TSUYAMA
TO OKAYAMA
   SYNYO LINE
TO OKAYAMA
                        TATSUNO
        NAKAI BRIDGE
         1
                                               HOMERE BRIDGE

                                                 EIKYU BRIDGE
                                                          JO HIMEJI
                                            HONKYU BRIDGE
                                                      TO KOBE
                         KAMIGAWARA
                         INTAKE WEIR
          TO KOBE
MANAGO BRIDGE
 KAMAE
9,10, II,I2

    KAMIGAHARA
   A WATER QUALITY MONITORING STATIONS

   • BOTTOM SEDIMENT MONITORING STATIONS

               Figure 2.  Major monitoring stations.
                                71

-------
   TABLE 4.   THE CHANGE  IN  WATER  QUALITY  WITH TIME AS ANNUAL MEAN


Item
pH
DO
COD
BOD
o
c
3
+>
(O
i
1
O)
ฃ
o
1 	 1
SS

_
Cl

NH4-N

N02-N
N03-N
NH4-N+
N02-N+
NO *




Item
PH
DO
CD
rd
ro
s_^--
O)
Cฃ.
T3
• i —
>
COD

BOD
SS
Cl~

NH4-N
N02-N

Unit


mg/1
mg/1
mg/1
mg/1


mg/1

mg/1

mg/1
mg/1

mg/1
-N



Unit


mg/1
mg/1

mg/1
mg/1
mg/1

mg/1
mg/1

)

7
9
3
3
10


12

0

0
0

0





9/1

.5
.8
.2
.1



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.07

.020
.20

.290




1971

10
0
148

233
172
472

28
0

.3
.9






.0
.048

1972

7.4
10.4
3.0
2.0
7


16.3

0.12

0.038
0.26

0.418




1972

10.5
2.1
81.4

145
99
342

10.8
0.101

1973

7.4
10.8
1.5
1.8
12


8.8

0.15

0.029
0.43

0.609




1973

10.8
1.3
72.1

223
156
434

15.7
0.012

1

7
10
1
1
17


6

0

0
0

0




Year
974

.4
.0
.8
.6



.8

.11

.008
.53

.648



Year
1974

10
1
62

268
142
377

15
0

.2
.8
.4





.0
.057

1975

7.3
10.1
0.9
1.5
12


6.4

0.09

0.008
0.79

0.888




1975

10.4
1.0
65.9

182
252
399

13.9
0.093

1976

7.4
9.9
1.6
1.5
19


5.8

0.06

0.009
0.58

0.649




1976

10.7
0.3
123

231
248
458

16.6
0.028



7.4
10.4
1.4
1.8
7


6.2

0.11

0.012
0.68

0.802




1977

10.6
0
204

236
372
710

23.6
0.013
N03-N   mg/1       0.19    0.18    0.18    0.34     0.93     0.01     0.15

NH4-N+
 N02-N  mg/1      28.238  11.081   15.892  15.397   14.923   16.638   23.763


                                72

-------
TABLE 4.   (continued)
Year
Item
PH
DO
(O
fO
s
(O
en
i

-------
 mg/l
  12
  10
        PH
300
200
 100
    _  SS
200
 100
      BOD
	TATSUNO
	KANAE
	KAMIGAWARA H
                 N	
      l    I    I   l
                    V
                        I	I
                 I    1    I
                   mg/
600
                  400
                                200
                l   r
       Cl
                    12
                     8
                                         I    l
                      -   DO
                         I   I
                   30
                                 20
                    10
                               I    T
    _ NH4-N+N02+ N02-N+N03-N_
    1971  72  73  74  75  76 77      1971  72  73  74  75  76 77
                             YEAR
 Figure 3.  The  change in water quality  over time (annual mean value)
                                74

-------
     The SS value  at  Tatsuno,  low at 7-19  mg/1,  shows no tendency to change.
At Kamae,  SS  levels  ranged  between  99-172 until  1974.   Since  then  the level
has  increased  rapidly to 372  mg/1  in 1977.  At Kamigawara, SS  levels  were a
little  higher  (by 5-10 mg/1)  than at Tatsuno,  but compared to  the  other en-
vironmental factors   little  influence from the  Hayashida River  is  observed.
This may be caused by the effects of settling as the river flows downstream to
the station.

     The Cl"  value at  Tatsuno is 5.8-16.3 mg/1.  Its average  value over the
past  seven  years  has  been 9 mg/1,  which is  normal  river water quality.  The
minimum value at Kamae was  342 mg/1  in  1971,  but since then has increased to
almost  twice  that figure  (710 mg/1  in  1977).  This was  caused by wastewater
discharge  from  the leather  industry where salt was being  washed from hides.
The  Cl   is different  from other  factors since it is  not physically and bio-
logically  decomposed.   The  Kamigawara   station was  directly affected  by the
Hayashida River  and  after  1975, the chloride at Kamigawara increased to about
ten times that of Tatsuno.

      Inorganic nitrogen  values for  NH4-N and N02~N  at Tatsuno  are relatively
small,  but  N03-N has  increased rapidly  from  its  minimum  of 0.2 mg/1 in 1971.
N03-N is the  final decomposition product for  inorganic nitrogen.  The ratio of
NQ3-N to total  inorganic nitrogen is largest  at  Tatsuno.   In  contrast, inor-
ganic nitrogen at  Kamae is  11-28 mg/1,  of  which  NH4-N is more  than 90%.  The
N03-N  at Kamigawara  is almost the  same  as  that of  Tatsuno,   but  the NH4-N
increases by  1.5-2.0  mg/1  due to the  influence  of the Hayashida River.  From
these facts, it may be concluded that biodegradation does not reach the nitri-
fication stage  during  the  1/2 km it takes the  river to  flow from Kamae to
Kamigawara.

     Another  investigation  of water quality conducted on the  Hayashida River
showed  that the  total phosphorus (0.2-1.7  mg/1)  is  relatively  small compared
with  BOD.   This  may  be caused by  domestic wastewater.   But  total  chrome is
also  relatively  high  at  1-10 mg/1 of  discharged water.  Thus, the water pollu-
tion in the Hayashida  River is mainly caused by the  leather industry.


BOTTOM SEDIMENTS IN THE IBO RIVER

     Since there  is  no specific pollution  problem in  the middle and upstream
of  the  Ibo River,  the  discussion will  be confined  mainly to  the  Hayashida
River and  the  confluence with the main  channel  where  the water is badly pol-
luted by the leather industry.

     In this investigation,  pH, COD,  volatile and  fixed material, total nitro-
gen,  total  phosphorus,  sulfide, total chromium, water content  and grain size
composition  were  measured  as  bottom sediment  characteristics.  PCB,  total
mercury,  al kyl-mercury, cadmium,  lead,  cyanogen  (CN)2,   arsenic,  hexavalent
chromium and organic phosphate  were measured in elutriate tests.

     The Hayashida River has  a steep bed  with a slope  of about 1/300.  The
flow  velocity is  very high.   Consequently,  suspended solids or minute sludges
may  not  settle,  but  organic  sludges  generated  from  polluted  wastewater
                                      75

-------
will accumulate at weirs and at the confluence where the velocity is reduced.

     The "sludge" component of the bottom sediments has a low specific gravity
of 1.78-1.90.   The water content is high at 63.1-90.3%.  m = —  where-
                                                          wt
                    m  = water content, wet wt. basis
                    Ww = weight of water
                    Wt = total wt. of soil

Clay and silt  with  a diameter of less than 74 M make up 75-95% of the sludge.
The unit volume weight is small  at 1.02  g/cm3.

     The  sand-gravel   component   in  the bottom sediments  is  65-94%  gravel
Specific gravity is  in the range of 2.64-2.68.

     Figure 4 shows the relationship between COD and volatile  and fixed matter
in the  bottom  sediments of the  Hayashida River.  The volatile and fixed sus-
pended  matter  in the  sludge differs  from  that in the  sand-gravel  component.
In the  former,  it varies  from  8.8% to  68.6%,  but  most  fall  into the ranqe of
40-70%.

     The COD  value is also  separated  into the two  components.   It  is in the
range of 11  mg/g to 290  mg/g dry weight in the sludge but mostly in the range
of 40-300 mg/g.  These results  show that the bottom sediments  of  the Hayashida
River are composed of organic sludge with a large amount of volatile and fixed
matter and  COD.

     Sulfide content  is  small   (about  40 mg/kg,  dry weight)  upstream of the
Hayashida River.  It  increases  to 417 mg/kg  in the  lower stream and near the
confluence it  is  1,090 mg/kg.   This shows  that reduction  is  occurring during
stream flow.

     Depending upon the location, the total chromium content is 1,300 mg/kg to
21,000  mg/kg.   This is caused  by the  leather industry  wastewater  which in-
cludes  protein  compounds  and  chromium resulting   from  the   leather  tanning
process.  High nitrogen content  of 605-22,100 mg/kg dry weight and phosphorus
content of  850-2,780 mg/kg  also exists.

     The results  of the  elutriate tests showed the  leaching  rate to be lower
than  the  limit of  quantative analysis  for all the  tested  items,  as shown in
Table 5.
 THE WATER POLLUTION MECHANISM AND CONTROL MEASURES CRITICAL IN THE IBO RIVER

WATER POLLUTION MECHANISM

     As  discussed  in  the  previous  section,  water pollution  in the  Ibo is
caused  by wastewater  from  industry  along  the Hayashida River.   Bottom sedi-
ments  accumulate  around weirs  and  at  the confluence of  the  two rivers where
flow velocity is reduced.
                                     76

-------
mg/g
300
200
100
50
COD
r\s\
20
10
5



1
i i i t i i i
4(5 -
O SLUDGE 76Q <53 -
A SAND GRAVEL 5
8
O
,O l2
1 Q)n
09

SEDIMENT REMOVAL THRESHOLD
OlO
2
0
A
A A
AAA
A
1 1 1 1 1 i 1
                          5      10  1520   30   50     100
                          PERCENT
Figure 4.  COD and volatile and fixed material  in sediments.


                             77

-------
                 TABLE 5.   ELUTRIATE TEST OF SURFACE SEDIMENT

Monitoring Poi
Item
T - Hg
R - Hg
Cr6+
Pb
Cd
As
Hayashida
River
mg/1
mg/1
mg/1
mg/1
mg/1
mg/1
not
not
not
not
not
not
detected
detected
detected
detected
detected
detected
nt
Confluence of
the Hayashida
and Ibo River
not
not
0.
not
not
not
detected
detected
0005
detected
detected
detected
Limit of
Quantative
Analysis
0.0005
0.0002
0.005
0.01
0.005
0.01
Minimum
Acceptable
Level
0.005
N.D.
0.5
1
0.1
0.5
Org.
Phosphate mg/1
CN

PCB
mg/1

mg/1
not detected  not detected     0.005

not detected  not detected     0.03

not detected  not detected     0.005
1

1

0.003
Ref:   The method for performing tests is given in notice
      No.  14 of the Environmental  Agency.
      The  poor water  quality  of the Hayashida affects  that  of the lower main
 Ibo  and polluted sludge moved  by  floods  further aggrevates the water quality
 of  the  lower stream.   The  deterioration  in  the river  water,  together with
 polluted  bottom sediments, has  affected  agriculture and industry.  It  causes
 eutrophication,  DO reduction  and  some anoxic conditions which  result  in the
 death of  aquatic organisms.   This pollution mechanism  is diagrammed in  Figure
 5.

      A  variety  of approaches  should  be  followed  in cleaning  up the  river,
 including  restriction on  discharge  of industrial wastewater,  installation  of
 sewage  treatment facilities  and industrial waste, introduction  of clean water
 to the  polluted  river and  dredging of  bottom sediments  to enhance  the capacity
 of the river for self-renewal.

      These  steps  have  been  or  are  now  being   taken.   Wastewater discharge
 restrictions  have  been  applied  to all  local   industry  and installations  of
 pre-treatment facilities are now occurring.

      In  Tatsuno  City, the construction of public sewage facilities is  making
 steady  progress.   In the  upper Hayashida,  construction of  a  dam  has been
 launched to control the stream flow.
                                     78

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1


1
WATER QUALITY
DETERIORATION

v
WASTE INFLOW



*
DETERIORATION
OF ENVIRONMENT



BLUDGE
ACCUMULATION
 DECREASE OF
   AQUATIC
  LIFE — DEATH
 DECLINE
    IN
USEABILITY
             POLLUTION OF
             BOTTOM SEDIMENTS
DETERIORATION
 OF WATER
  QUALITY
                                                               OC.
                                                               U
                                  X
                                  cn
RE-POLLUTION
              POLLUTION OF
            BOTTOM SEDIMENTS
       EUTRIPHICATION
         BY AQUATIC
      MICROORGANISMS
                                                               DC
                                                               UJ
                                                               >
                                                               a:

                                                               o
                                                               CD
        CHANGE IN
          FISH
         SPECIES
             ACTIVE
          AVOIDANCE OF
              FISH
               DEATH OF FISH
      Figure 5.  Water pollution mechanism in  the Ibo River.
                               79

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CRITERIA FOR REMOVAL OF ORGANIC SLUDGE

     Although organic sludge  is  detrimental  to the environment  there  are yet
no rules to  judge  whether river bottom dredging is necessary.  However, fixed
dredging criteria have been developed for major ports.

     Provisional standards  for  removal  of  organic sludge  have been  set by
Hyogo Prefecture so that dredging can be performed as  a eutrophication control
measure.  According to these  standards,  the  necessity for removal is based on
three criteria:  1)  volatile and  fixed  suspended matter, 2) COD and  3) sul-
fide.   Sulfide  can be omitted  from the standards  for rivers  because little
sulfide formation occurs  in fresh water.

     Levels  of  15% volatile  and  fixed  suspended matter and  20  mg/g COD (dry
weight)  are  set as the  standards.   If  one of these criteria is exceeded the
bottom sediment should be removed.

     The sand-gravel component  does not need to be removed but  almost all the
sludge  should be dredged,  as shown in Figure  4.   As  a consequence, the major
area to  be  dredged is  around the  confluence  where  the average  depth of accu-
mulated  sediments  is  0.8 m,  the total area  is 6,300  m2,  and the total volume
is 5,000 m3.  Elsewhere  in  the Hayashida River there are  about 3,000 m3 of
accumulated sediments.
                         DREDGING OF BOTTOM SEDIMENTS

     In dredging  organic  sludge,  secondary pollution must be avoided.  In the
selection and  adoption  of a plan for dredging, sludge treatment and disposal,
individual  processes  must  be considered  as  components  of a  total  process.
Figure  6  shows  a  total  process  beginning  with the  dredging of  sludge and
sediment and with  final disposal.

     This total process  is divided into five major  steps:

     1)   Prevention of  Dispersion  of Pollutants

     2)   Dredging and Removal

     3)   Treatment

     4)   Final Disposal

     5)   Environmental  Monitoring

     After  various  laboratory  and field  tests  were  conducted,  integrated
examination and analysis  resulted in the following proposal  for each step:

     1)   Dispersion Prevention:   use of silt protector

     2)   Dredging  and  Removal:   use  of vacuum collector and dump truck moun-
          ted receiver tank
                                     80

-------
               ,      i SELECTION OF REMOVAL AND \.
               1      l TREATMENT METHOD
                       DISPERSION PREVENTION
                       DEWATERING AND
                       CONCENTRATION
                WASTE WATER
            WASTEWATER
            TREATMENT
                                                        WASTE GAS
                                                        TREATMENT
    SOIL
CONDITIONER
EXHAUST
  GAS
                             RECLAIMING
5  FINAL
   DISPOSAL (  DISCHARGE
                      Figure 6.   Sludge removal  process,
                                  81

-------
     3)   Treatment:   combination of  natural  dewatering at dry river  bed  and
          use of chemical solidifiers

     4)   Final  Disposal:  landfill disposal by dump truck

     5)   Environmental  Monitoring:   monitor water quality  of  dredge area  and
          work only in winter to avoid odor problems


PREVENTION OF POLLUTANT DISPERSION

     Tests were  performed  in winter.  The "Provisional guidelines  for treat-
ment and  disposal  of bottom  sediments containing toxic  substances"  provided
baselines  for  judging  water quality  and  bottom sediments  before,  during  and
after the  dredging.  Basic  and  supplementary  monitoring points were installed
beforehand.  At the same time,  water pollution inside and outside of the silt
protector was monitored to judge the  performance of the silt barrier.

     One result was that the turbidity around  the suction  nozzle of the vacuum
collector was greatly affected by water depth.  When  the water  depth was about
10 cm,  average  turbidity was  as high  as 653 degrees,  but it was  about  179
degrees when the water  depth  was 20-40 cm. The  turbidity before  the work  was
74-143 degrees.   When water depth is shallow,  extreme care must be taken.  The
turbidity  inside and outside  of the silt protector was  smaller than the tur-
bidity measured before  the  work at  the upper and lower water layer.  The silt
protector should be installed in a closed loop  so that currents cannot


DREDGING AND  REMOVAL

     In dredging  organic  sludge  it  is important to  prevent secondary pollu-
tion.  Disturbance of the  sludge must therefore be minimized.   To  reduce  the
volume of wastewater  after the dredging, the concentration of dredged material
should be kept as high as possible.

     Taking these  factors  into  consideration, the dredges which could be used
in the Ibo  River would be the following:

     1)   Pump dredge (with  vacuum collector)

     2)   Grab dredge (with  closed grab bucket)

     3)   Bulldozer (amphibious)

     4)   Others

     In selecting  dredges,  many factors such  as  influence on the  environment,
ease of  use  and economy  were  considered.  The vacuum collector  mounted on a
truck with a receiver tank carrier for transportation of dredged sediments  was
adopted.   In conducting tests,  a 100 ps vacuum collector with  a  suction head
having either 0.08 m  x  1.0 m  rectangular opening or a 0.23 m  diameter round
opening  was   used.   The apparent  average  sludge  concentration  rate  was  in
                                     82

-------
the range of  51%  for the rectangular type,  and  69% for the round type.  When
the depth  of  sludge accumulation  is  about 20  cm,  the  rectangular  suction
mouthpiece  is best  suited;  for 40-60  cm,  the  round  one  is  more  effective.
Soundings showed condition of the river bottom after dredging was in very good
shape.

TREATMENT

     Dredged  sludge  contains  a large  volume of water  and its  fluid  nature
causes  problems  in  transportation to  the  dumping site.   After  natural  de-
watering using  a  dry river bed, chemicals are used to solidify the sludge for
transporting.

     Using  sludge  samples with  water contents of  300%  and  600% (dry  wt.
basis), solidification tests were conducted using Portland cement and fly ash.
The results are shown in  Figures 7 and  8.  In spite of the large difference in
water  content,  there was  no significant difference  in  the  strength per unit
area.   The  more solidifier  used  and  the longer the  curing  time,  the  greater
the strength.

     The  unconfined  compression  strength   of   a  cylinderically molded  soil
sample could  not  be  measured.   Although bottom  sludge with  an extremely high
critical ratio  was  composed primarily  of organics,  it  was relatively  easy to
treat.

     In  the field test,  dredged sludge was  put  into a storage basin in a dry
river  bed,  and the  stages of  the natural   dewatering  process were observed.
After  that, solidification tests were  carried out.  Table 6 and Figure 9 show
the change of  water content  in drained sludge  with time.

              TABLE 6.  CHANGE IN WATER  CONTENT OF DREDGED  SLUDGES.
                    Elapsed Time	Water Content
0
3 days
7 days
14 days
28 days
1,640%
1,090%
500%
370%
260%

     As  shown  in  Table 6, the  natural  dewatering  is very effective, particu-
larly  in  the first week.  Although a blind culvert was installed in the sludge
storage basin, most of the water permeated through the silt and a small amount
came through the blind culvert.

     The  quality  of  water  permeating through the blind culvert was analyzed.
The  turbidity  was very  high,   and  also the  values  of BOD  and  normal hexane
                                       83

-------
        (FAST-SETTING PORTLAND CEMENT)
             WATER CONTENT
             600% 7 DAYS
      •	• 600% 28 DAYS
      A	A 300% 7 DAYS
       ;	A 300% 28 DAYS
 oi—V
           10
           15
20
25
30
Figure 7.
   DOSAGE RATE OF SOLIDIFIER
            (PERCENT)
Relationship of solidifier dosage and strength, for curing times
of 7 and 28 days.
                         84

-------
CM
 O
   A
 (T 4
 h-
 (f)

 2
 O
 cc
 CL
 ^
 O
 UJ
 2
 U.


 8
   o
     FLYASH:

     I5P/0 7 DAYS

—*  15% 28 DAYS

  O  30% 7 DAYS

     30% 28 DAYS

     50% 7 DAYS

—T  50% 28 DAYS
    0        5        10       15       20       25

         DOSING RATE OF SOLIDIFIER (PERCENT)

         SOLIDIFIER: PORTLAND CEMENT

         WATER CONTENT: 600 PERCENT

 Figure 8.  Relationship of dosage rate of solidifier and strength, for
         7 and 28 days of curing.
                           85

-------
ฃ40

Ld
a 30
o
o
CO
u_
o
Q.
LU
Q
   20
   10
    0
               SLUDGE STORAGE BASIN

              (I)
                     V
      	(IV)
      	-(Ill)
                              1500
                                                      1000
                              500
                                   f-

                                   LU
                                   CJ
                                   cr
                                   LU
                                   Q_
                 LU
                 h-

                 O
                 O

                 (T
                 UJ
                              0
         0
4       6
 DAY
114
28
  Figure 9.  Change of depth of bottom sediment and water content with
          elapsed time.
                              86

-------
extraction materials, but  nine  other tests of water quality relating to human
health satisfied the discharge standards.

     To  obtain  better  water quality  during operations  it was  necessary  to
adopt  sand  filtration for  the  blind culvert.  Also, when  the  sludge storage
basin  is  used more  than twice,  it has to be dug to a certain depth because of
clogging.

     In  field tests  using  fast-setting Portland cement as  the  solidifier and
fly-ash as an additive, a backhoe was used to mix the material for a period of
10  days.  Unconfined  compression  strength using Portland cement  and 20% fly-
ash was  as low  as 0.1-0.2  kg/cm2 for day 7, and day 28 was 0.4-0.7 kg/cm2.  In
the case  of  40% fly-ash day 7 was 0.2-0.3 kg/cm2 and day 28 was 1.1 kg/cm2 as
shown  in Figure 10.  The  critical   ratio  was in the range  of  1.5-4.0  in the
latter case.  The volume was increased by about 18%, when 40% of the additive
was used.
FINAL DISPOSAL

     The  strength  needed  for  excavation,  dumping and
sludge  is 0.3  kg/cm2  for  excavation  and loading, more
transportation  and  dumping,  0.8 kg/cm2 for covering, and
ing after reworking  the soil.
           covering of  treated
           than  1.0 kg/cm2  for
           1.0 kg/cm2  for bank-
     Because  the solidified  sludge was  intertwined  with animal  hairs  that
existed  in  the  bottom  sediments,  the  necessary  strength for  excavation and
loading,  transportation  and dumping, covering, and  banking  were respectively
0.1-0.2  kg/cm2,  0.4 kg/cm2  or more, 0.3  kg/cm2  or  more, and  0.5  kg/cm2 in
terms of the strength after disturbance.
     The most economical conditions that met these figures are as follows:
     1)   Solidifier
Fast-setting
Portland cement  li
     2)   Additive
fly-ash
20%
     3)   Curing time
not less than    28 days
     4)   Water content of treated sludge  :    not more than
                 70%
     Ref:  Above conditions are based on sludge with an initial water content
           of 500% and the use of a backhoe for mixing.

     Before  covering  operations  began  it is  necessary  to wait  for natural
de-watering  at  the  dumping  site as well as for the recombination of soil par-
ticles,  since  the  strength  does  not  reach  0.3 kg/cm2 at  the  time of trans-
portation.   From the test data on the critical ratio, solidified sludge cannot
be  used  for banking materials.  It  cannot   be  used  as backfill  material  in
revetment, for the same reason.
                                      87

-------
    1.5
CM
w 10
cc l.u
LU
CC
0.
   0.5
Q
LU
8
    o
         FLYASH CURING DAYS (%)
1
      0         5        10        15       20      25

      DOSAGE RATE OF FAST-SETTING PORTLAND CEMENT
                          (PERCENT)
  Figure 10. Unconfined compression strength and dosage rate of solidifier for

          7 and 28 days of curing.
                           88

-------
     Consequently,  dumping  in  dry river  beds  or  transportating  them to  a
neighboring  land  reclamation  site  and  covering the surface with  better soil
may be the  only possible way of final disposal.


ENVIRONMENTAL MONITORING

     Downstream of  the  dredging site  are industrial water  intakes  and a com-
mercial  fishery.  Careful monitoring  is necessary to avoid  the  generation of
secondary  pollution  by dredging  which  would have a negative  impact  on these
water  users.  As  mentioned  earlier,  the water quality has  been  monitored  for
several  factors such  as turbidity, pH,  BOD, COD, normal  hexane extraction and
DO at  basic  and supplementary monitoring points installed downstream from the
worksite.   Downstream  samples  are compared with  control  samples  to prevent
water  quality  deterioration due to dredging.-  The  installation  of  the closed
silt protector proved to forestall such problems.

     Odor  monitoring  is  also  required.   During  the  field  tests in  winter
neither  H2S  nor  methyl  mercaptan were   detected  at a  distance of  5  to 50 cm
from the surface  of dredged sludge in the disposal basin.  When heated inside
to 30%C, 5 mg/1  H2S was detected.  A threshold concentration for human health
is 10-15 mg/1.   At this level,  H2S will cause eye irritation within 6 hours.


                                  CONCLUSION

     The particle  size  distribution  curve  for  bottom  sediments  before  and
after  the  test  dredging is  shown  in Figure  11.  The bottom sediments prior to
dredging are  composed  mainly  of minute  particles; after dredging they consist
more of coarse particles.

     The cost  for  dredging depends on  site and  volume.  A  rough  estimate is
about  8,700-10,000  yen  per  cubic meter, of which the solidification treatment
costs 3,700 yen.

     In  conclusion, after extensive laboratory and field tests, useful knowl-
edge has been obtained which is applicable to actual dredging.
                                      89

-------
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                        POLLUTION CONTROL IN TOKYO BAY
                        Masai  Yako and Keitchi  Akimoto
                     2nd District Port Construction Bureau
                         Ministry of Transport, Japan


                                 INTRODUCTION

     This  report  indicates the  distribution  and  properties  of  the  sapropel
which has  accumulated  in  Tokyo Bay, clarifies  the effects of this sapropel  on
water quality and the  biota and investigates the results of dredging designed
to control  pollution from this source.
                            POLLUTION IN TOKYO BAY

BOTTOM DEPOSITS

     Sapropel is a soft mud, containing large amounts of organic detritus such
as algae, pollen, spores or animals.  Sapropel accumulates under reducing con-
ditions  (anaerobic  areas)  in  calm  sea areas.   The  sapropel was  found  to be
widely distributed  from  off  Haneda  to the middle  of the bay with a thickness
of 40-50  cm  (Figure 1).  Samples of  sapropel  and the underlying mud, 50-80 cm
thick, were  collected  together without disturbing the  layers and  the samples
were analyzed.

     The  conditions of  the  bottom  deposits  were  classified according  to 1)
surface  layer,  10 cm down from the top of the sapropel, and 2) substratum, the
clay and silty layer 50-60 cm below the sapropel  (Figure  2).

     Analyses  of  the  deposits showed that the  surface  layer had higher values
than the  substratum with respect to water content, sulfides, ignition loss and
chemical  oxygen demand (COD).   There was also  a remarkable  amount of organic
pollution  in the  surface layer in  the  innermost part of  the bay.  In addition
to these  organic  pollution indices,  the  nutrient  content (nitrogen and phos-
phorus)  was  high  and  matched the areas where the sapropel was thick (Figures
3-8).


WATER QUALITY

     In  summer there  was  a  thermocline  and halocline  at depths of  5-10 m.
Water  quality  differed remarkably above and  below this  layer.  pH was high in
the  surface  layer and tended to be  low in the  bottom layer.  Dissolved oxygen
(DO)  was supersaturated in  the  surface layer,   while the  bottom  water  in the
innermost  and  middle  parts  of  the  bay  was poor in  oxygen.   COD  and total

                                       91

-------
               Arakawa  Nakagawa
Sumidagawa River —— River    River

      TOKYO

   SHINAGAWA
      HANEDA

   Tamagawo River

   KAWASAKI
                                           Edoqowa River
                                                      CHIBA
                          O) 10 O  *•
                              00  • O
                     •  o o  • •  o
                    o  • •   •
       OKDHAMA
  HONMOKU
   TOMIOKA
        YOKOSUKA
                          FUTTSUZAKI
                                             ANEGASAKI

                                     BANZUNOHANA


                                     KISARAZU
  KANNONZA
                                     • 0.1-0.3
                                     0 0.3-0.7
Figure  1.  Distribution and thickness of sapropel in Tokyo Bay (in meters)
   SEA BOTTOM
  Figure 2.
  Diagram of core
  sample.
                      FLUID MUD
                         J  J_SURFACE  (0-IOcm)
                        SAPROPEL
                        J_
                         I
                        50 (cm under sapropel)
                             SUBSTRATUM (10 cm)

                              92

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-------
organic carbon  (TOC) were  also  high in the  surface  layer  and low in the sub-
stratum.   These results  indicate  that  above  the thermocline the water is rich
in orgam'cs.

Nutrient concentrations  were  high  in  the coastal  regions  but  tended  to  de-
crease towards  the  mouth of the bay.   There were high  values  for phosphorus,
in  the  form   of  phosphates  (P04-P),  and  nitrogen  in  the  form of  ammonia
(NH4-N),  in the water directly above the  sea bed,  corresponding to the zone of
oxygen-poor water  (Figures 9-11).

BENTHOS

     Sampling  was  performed  twice with  a  Koken  mud  sampler.   This  device
samples an  area of  1/15 m2 with  a sample  size  of 5.6  1.   The macrobenthos
retained on 1 mm-mesh sieve was identified  and counted.

     In the summer  survey,  areas  totally  devoid of  life were  observed in the
innermost and  middle parts  of the bay.  Only one or  two  organisms were found
nearby.  The species found included polychaetes  and  mollusks in the middle and
mouth  of the  bay  and crustaceans  at the mouth of the bay.   There tended to be
greater  diversity  toward  the  mouth of the  bay (Figure  11).   In the  winter
survey, there  were  no  areas devoid of life,  but there were many places in the
inner  bay where only two or three organisms were found.   This was correlated
with the  spread of organic pollution.

     Figure 12  shows the relationship  between the benthos  and the values for
COD, sulfides  and  ignition loss in  the mud  deposits of Tokyo  Bay.

     According  to  these results,  polychaetes  gradually  decreased  when  the
value of COD fell  below  15 mg/g, sulfides  fell  below 0.5 mg/g and the ignition
loss fell below 10%.

     In the case  of crustaceans,  maximum  numbers were  seen  at a COD of about
13  mg/g,  sulfide  content  of  0.25 mg/g and  an  ignition  loss of  about 7.5%.
When these values  became higher or lower, the number of crustaceans  decreased
as  well as  percent  contribution to the population.   This  suggests  that there
are optimum values for crustacean success.

     The total number  of benthic  organisms,  the number  of  species  and  the
biotic index  (BI)  showed optimum  values  for a  COD  of 8-10 mg/g, sulfide con-
tent of 0.3-0.5 mg/g and  an ignition loss of about 5%.

     Figure  13 shows  a histogram  correlating  the  number  of species  in  the
benthos with the  values of COD, sulfide  and ignition loss  and mud deposits in
a  survey of Tokyo Bay conducted in October, 1972.  According to these results,
the number of  species reached a maximum at a COD of  5 mg/g, sulfide content of
0.25 mg/g  and  an  ignition loss of  about  5%.  When  these  results are compared
with  the  present  surveys,  the  COD value  is seen  to  be rather  low,  but the
sulfides and  ignition  loss  values match  closely the  best  conditions from the
standpoint of the  benthos.
                                      96

-------
                                                           • 1-50

                                                           o 50-111
   0


   10


  20


  30


  40
   0


1  10
a. 20
UJ
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  30
  40
   0


  10


  20


  30


  40
                  Figure  9.   Sampling stations for water quality gradients.


      15  29 48  69  90
                                     NUMBER
                     15  29  48 69  90     15  29  48  69  90     15 29  48 69  90
 o 21
WATER TEMP (ฐC)'^
           i '   i
                                	i
                    ^ .04:10
                     O.IO-.70
                     COD(ppm)
                                 J	L
          .•.OI-.09-
           0 .09-.20"
           .O-N/ppn))  V-^
_• .01-09
 O.IO-.20  •'•  ^^
 P04-P(ppm)  ••••'7*-
 9   (f
        I	I
                     TOC(ppm)
                     I    I   I
J	I
     Figure 10.   Vertical  profiles  along the  longitudinal  section  delineated in
                  Figure  9.

-------
                                       3) LOCATION OF NO
                                          LIVINGORGANISMS
Figure 11.   Distribution of benthic  species composition  September 1977.
                                  98

-------
 ฃ   2i
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40
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- 80
-
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- O
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-
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-
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- 60
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                                          20
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I20rl20r200r 60r  I2r
 80
 40
       -100 -
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 80
       -100-
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h40
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                                                                5             0 IGN.LOSS(%)

  Figure 12.  Correlation between  zoobenthos and  COD,  sulfide and  ignition loss.


                                            99

-------
         60
         30
      en
              IGNITION  LOSS(%)
      5    20
      u  60
      Q.
      en
15
10
      0  30

      oc.
      UJ
      CD
         60
         30
             SULFIDE (mg/g)
             COD (mg/g)
           40     30    20     10     0

Figure 13.   Histogram correlating benthic species with sediment values.
          1m
                -20cm
                                    WATER SAMPLER


                                     D.Q  METER
                            -—ACRYLIC PIPE

                            WATER (about 20:1)
                             30cm
                       Figure 14. Leaching experiment
                                 apparatus.
                               100

-------
                  EFFECT OF BOTTOM DEPOSITS ON WATER QUALITY

     There are  two  ways  in  which bottom  deposits  affect water quality  -  by
leaching of  organic  matter and  nutrients  from the  deposits, and by  the  con-
sumption of dissolved oxygen from the water.

     In Japan  there  have  been  few  experiments  on  the  amounts  of  substances
leached into the  sea,  and there is  only a  general  notion of the way the  con-
tents  and  temperature  of  organic  matter and  nutrient salts in the  mud,  and
dissolved oxygen  in the water just above the sea bottom, influence  the leach-
ing process.

     There are  often cases where deposits  consume the dissolved oxygen in the
water  and  the  oxygen-poor conditions which produce  a cyclic pattern promoting
further  deterioration   of the  deposits,  lower  water  quality,  and  adverse
effects on the  benthos.

     In  the  leaching  experiments,  samples  were  taken  simultaneously  from the
surface layer  of  the  deposit (1-30 cm) and the substratum (50-80 cm under the
sap^opel).  The water  directly  above the bottom was also taken for  use in the
experiment.  Figure 14  shows the experimental  apparatus.

     The  experiment  was  performed  for five  days  and the  amount  leached per
unit area per day (mg/m2/day) was calculated from changes in the concentration
in  the water.   The  average  amount  leached  was the  average of these  daily
values.

     The average  values  obtained in experiments performed in September,  1976,
and  September,  1977,   are  shown in  Table  1.   Large  differences  were observed
between the surface layer and the substratum.


                    TABLE  1.    AVERAGE AMOUNTS LEACHED (mg/m2/day)
                                   COD    TOC       T-N       T-P


                    Surface layer  285    192       145        27

                    Substratum     232    125       136        10
OXYGEN CONSUMPTION RATE IN THE DEPOSITS

     The  samples  and j_n  situ  seawater for this  experiment  were  collected by
the same  method  as used in the  leaching  experiment.   After  they  were brought
to the laboratory, they were reaerated in a constant temperature chamber (20 ฑ
2ฐC).   The  experiment was_  started  when the DO  concentration  in  the seawater
increased.  The  DO and  S~  concentrations  in this water were  measured  at in-
terval s.

                                      101

-------
     The experiment  was  performed  for  five  days and the average  oxygen  con-
sumption was calculated  using  the same  method as in  the  leaching experiment.
The S  ioji was converted to oxygen iji the. ratio of 2 moles of 02  produced  to 1
mole of S  , based on the equation S04~ ^ S  + 202 (gas).

     The results gave  an  average  oxygen consumption rate  of 2.5g 02/m2/day in
the  surface  layer  and  1.32g  02/m2/day  in the substratum.   The  surface  layer
consumed 1.7 times more  oxygen than the substratum.  These  results  show  that
the  sapropel has a  deleterious effect on the aquatic environment and that the
environment can be restored by removing the  sapropel.
                     THE RESULTS OF REMOVING THE SAPROPEL

     Seawater purification can  be  broken  into two types -  biochemical  purifi-
cation produced  by  microorganisms,  or physical purification  such  as  seawater
exchange.

     The  use  of  microorganisms involves  their  ingestion  of organic  matter
present in the water.   Part  of  this matter is  converted to  substances neces-
sary for  the  growth  of the microorganism  and the remainder becomes a respira-
tion byproduct which is  oxidized  to inorganic material.  The bacteria even-
tually die and this  material  is utilized by other bacteria.   There is, there-
fore,  a  partial  change  to  inorganic material  in this  process.   The  organic
matter is  decomposed more quickly  as  the number of times the organic matter
passes through the bacteria increases.  When there are  protozoa or zooplankton
present to  feed  upon  these  bacteria,  the number of cycles  through organisms
increases and the organic matter is  decomposed  at a faster rate.

     This ingestion of organic matter by microorganisms is  part of the  process
by which  substances circulate in the water.  The way to understand the  process
of biological control  of organic matter is to  investigate the circulation of
organic matter in the  biota  and the cyclic rate.   Figure  15 shows the circu-
lation of organic material in Tokyo  Bay.

     Because this survey  was  conducted in summer when  there is  a lot  of tur-
bidity,  many  points  remain   unclear.   Various coefficients  of   the  material
circulation model were  determined  by site observations  and  laboratory exper-
iments.  The  idea  was  to  determine,  by  means  of  numerical  simulation,  what
degree of water purification can be  expected by the removal of  the  sapropel.
BASIC EQUATIONS OF THE EUTROPHICATION MODEL

     In the  preparation  of  the eutrophication simulation model, the following
five items had to be quantified to simulate the seawater turbidity mechanism:

     1)   The quantities of  COD and nutrient salts in the water which flows
          into the bay
                                     102

-------










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103

-------
     2)   The quantities of organic  matter  and  nutrient  salts which  leach  from
          the bottom mud

     3)   The rate of decomposition  of organic  matter

     4)   The rate of precipitation  of organic  matter

     5)   The rate of assimilation and absorption  by photosynthesis

These five parameters were quantified by means  of  field  and  laboratory  experi-
ments.

     Four substances were used as  indices in  the numerical analysis:  COD,  DO,
limiting organic nutrients (phosphorus) and inorganic  nutrients.   The circu-
lation process of these substances was expressed by developing  eight diffusion
equations, given below.   The following points were guidelines for  development
of the equations:

     1)   In the euphotic zone, there are diffusion, flow, production,  decom-
position, precipitation and an exchange between the surface  layer  and sub-
stratum.

     2)   In the aphotic zone, there are diffusion, flow decomposition,  pre-
cipitation, leaching from deposits,  DO consumption by  the deposits and  ex-
changes between the surface layer  and substratum.

     3)   Production involves the  assimilation  of  inorganic  nutrient salts  by
phytoplankton and their conversion into organic nutrient salts.  This results
in an increase in the COD and DO.

     4)   The inflow load refers only to flux into the euphotic zone.


     (A)  Diffusion Equations of Nutrients


          1)  Euphotic zone
         - yNo + LNo                                                     (1)
8NTh      3NTh     3NTvh     3      3Nr    3      3N
-งr  -~^-  -  1-   +3
      jh + pNon+ LNj                                                     (2)

                                     104

-------
     2)  Aphotic zone


3N'oh'   aN'oiTh'   aN'ov'h'.   3  ,u.u* 3lTo  ,   8   ,„.. ^3NTo .
~9t~	9^—      ay~   a^  (K  h ~^~  }  ay   C    ~W~)

   +Kz (No - N'o) -  pN'oh' + v (No - N'o) +  Bo                       (3)
 at           a          d      a        a              a


  +Kz (Nj - N'j) - pN'oh' + Bj                                       (4)



No   :  Organic nutrient concentration in euphotic zone

NT   :  Inorganic nutrient concentration in euphotic zone

N'o  :  Organic nutrient concentration in aphotic zone

N'y  :  Inorganic nutrient concentration in aphotic zone

K    :  Horizontal  diffusion coefficient in euphotic zone

K'   :  Horizontal  diffusion coefficient in aphotic zone

Kz   :  Exchange coefficient between surface  layer and substratum

a    :  Rate of photosynthesis

p    :  Rate of decomposition

Y    :  Rate of precipitation

p'   :  Rate of decomposition in aphotic zone

Bo   :  Amount of organic nutrient salts leached per unit time and area

BT   :  Amount of inorganic nutrient salts leached per unit  time and area

LNo  :  Amount of organic nutrient salts received from land

LNT  :  Amount of inorganic nutrient salts supplied from land

h, h' : Thickness of euphotic  and aphotic zones
                                    105

-------
u, u':  Flow rate in x-axis direction  in  euphotic and aphotic zones


v, v':  Flow rate in y-axis  direction in euphotic and aphotic zones








(B)  COD Diffusion Equations


     (1)  Euphotic zone
3Sh _   3Suh   aSvh   3 ,„.  3S,     3   ,„. 3S,    „   ,.

3F ~ " ~3F   "37" +3T~(Kh iV    3y~  (Kh 37;    Kz  (S
   + aaNjh - K^h -K3S  + LS                                         (5)






     2) Aphotic zone
                    SB                                              (6)
S    :  COD of euphotic zone



S'   :  COD of aphotic zone



a    :  Ratio of nutrient salt concentration  and COD concentration in

       phytoplankton



Kx   :  Reduction  coefficient in euphotic zone



K3   :  COD precipitation rate in euphotic zone



K\  :  Reduction  coefficient in aphotic zone



K'3  :  COD precipitation rate in aphotic zone



SD   :  Amount  of  COD leached per unit area and time
 D


[_-   :  Amount  of  COD load received from land
                                     106

-------
(C)  DO  Diffusion Equations

     (1) Euphotic zone


5Ch  =  Muh . |vh + ^_(Kh



     + K2 (C$ - C)h - K! Sh




     (2)  Aphotic zone
                                        (Kh   _j  _   Kz  (c .  r)  +  fa
                                                                    (7)
            'inr   ac'v'tr.   3  ,,,., ac;    a  ,Kh-_ac\  ,  k7  rr _
                  " ~        "   (Kh    }   "    (Kh ~)       (
at        ax         ay

  - Ki' s'h - DB                                                    (8)




P    :  DO release rate by photosynthesis

K2   :  Reaeration coefficient

C<-   :  DO saturation  rate

Kx   :  Deoxidation  coefficient

DR   :  Amount of DO consumption per unit area and time


DETERMINING THE COEFFICIENTS

     The coefficients used  in the calculations  were  derived as follows:

Production

     The production  rate was  calculated from  the  nutrient  salt  intake  of the
plankton obtained from an algal potential productivity (AGP) test performed on
surface  layer  water  collected  at  the site.   The average value  for the  whole
area was used.

Decomposition

     The rate  of decomposition was calculated from the difference between the
initial  concentration  and  the  final  concentration,  after  decomposition  in  a
dark room, using samples collected at each water level (both surface layer and
substratum).  The average for the whole area was used.

                                     107

-------
Precipitation

     The sediment sampler was  deployed  at the site  from  dawn  to sunset.  The
precipitates were then  collected  and  the concentration of specific substances
in the  precipitates  determined.   The  rate of precipitation was  calculated by
comparing water qualities in  the  same water  layer  for  both  the surface layer
and substratum.  The average value  for  the whole area was used.

Leaching

     Water just above the  sea bottom, and cores of  mud were  collected at the
site by  divers.   After  the samples were brought back  to  the  laboratory,  the
quantity  leached  was  calculated  from changes in  the  concentrations  of sub-
stances in the  collected  water.   The  value was divided over  three blocks for
the substratum.

Oxygen Consumption

     Samples were collected in  the  same way  as  for  the leaching test.  After
the samples were  returned  to  the  laboratory  they  were  reaerated.   The amount
of oxygen consumption was calculated from the changes in the  concentrations of
substances in the  collected water.

Influx Load

     The  actual   values  were  used  as  measured  in  1976  in  Chiba,  Tokyo  and
Kanagawa Prefectures.


RESULTS OF DIFFUSION CALCULATIONS

Validation by Hi storical Records

     Since the  1976  influx load  values were used,  a  companion  1976 investi-
gation of  water  quality (Figures  16-18) was used to check the validity of the
model.

     The coefficients used  in the model were obtained  from  surveys performed
in  September,  1976  and August-September,  1977.   These  values are  given in
Table 2.   The experimental  values were  corrected to those shown in the column
on the right  and are considered to  more closely resemble current values.

     The results  from the  model  equations are shown  in Figures 19-21.  These
results are outlined below.

COD

     In  the  surface  layer,  the isopleths  of 2  ppm and 3  ppm  generally match
current  conditions,  so  the accuracy  appears to be  good.  In  the  substratum,
the values currently are 2 ppm or less  near the center  of the bay.   The calcu-
lated  values  match those  from  the  mouth  to the middle  of the  bay.   But the
calculated values are  1-2  ppm higher than the current values in the innermost
part of the bay.


                                     108

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      40ฐ
50ฐ
140ฐ
40ฐ
50ฐ
140ฐ
40ฐ
30<
20ฐ
 10ฐ
       • 1.0-3.0
       O 3.0-7.3

         SURFACE
      	I	
                        40ฐ
                        30ฐ
                        20ฐ
              10ฐ
                   • 0.7-2.0
                   O 2.0-3.9

                   SUBSTRATUM
   Figure 16.   COD  (ppm)  average of July,  August, September  1976.
      40ฐ        50ฐ        140ฐ                40ฐ        50ฐ        140ฐ
40ฐ
30ฐ
20ฐ
10ฐ
                        O 0.050-0.280 _
                        40ฐ
                         30ฐ
                         20ฐ
                         10ฐ
                                    •  0.009-0.050
                                    O  0.050-0.179

                                    SUBSTRATUM
   Figure  17.   PO.-P  (ppm)  average of July,  August, September  1976.
                                      109

-------
      40ฐ
50ฐ
140ฐ
40ฐ
50ฐ
140ฐ
40ฐ
30ฐ
20ฐ
 10ฐ
       • 5.0-9.0
       O 9.0-10.9

       SURFACE
            I	
                       40ฐ
                        30ฐ
                        20ฐ
              10ฐ
                  •  0.9-3.0
                  O  3.0-7.7

                  SUBSTRATUM
   Figure IP. DO  (pprc)  average of July, August,  September 1976.
           SURFACE
    Figure  19.   Model  results for COD  distribution.
                                      110

-------
                    P04-P (ppm)
                    120 TIDAL
SURFACE

   Figure  20.
Model results for P04-P  distribution.
 SURFACE       J     120 TIDAL         SUBSTRATUM

  Figure  21.   Model  results for DO distribution,

                               111

-------
            TABLE 2.   COEFFICIENTS  USED  AS  MODEL  PARAMETERS.

Block
or
Coefficient layer
Production
amount Top
(/day)
Decompo-
sition K
<^!> Bฐ"ฐป
Precipi- Top
tation
amount
(m/day)
Bottom
Block
Amount 1
leached Block
(mg/m2/day) 2
Block
3
Block 1
Amount of Block 2
DO Block 3
consumption
(g02/m2/day)Total
area
Initial Total
value (ppm) area
Item
P04-P
COD
0-P
COD
0-P
COD
0-P
COD
0-P
COD
P04-P
COD
P04-P
COD
P04-P
DO
DO
concen-
tration
COD
P04-P
Experi-
mental
val ue
0.409
0.095
0.040
0.078
0.017
0.57
0.93
0.92
1.10
650
65
400
30
0
0
5.5
4.0
0
8.0
ppm
1.0
0.08
Current
Reason for Correction value
(used)
30% reduction; remarkable in- 0.29
crease in COD concentration in
top layer
0.095
0.040
Same 0.078
0.017
30% reduction; large precipi-
tation coefficient and drop in 0.40
concentration of water quality.
40% reduction (further reduction
made from 30% since reproduc- 0.56
tion of surface layer phosphorus
concentration still difficult).
30% reduction; large precipi-
tation coefficient and large 0.67
reduction in concentration of
water quality. 0.77
(Maximum leached value of 650
amounts 1976 and 1977 was 80% 65
of the value statistically.) 400
Same 30

INO UlbLllUULIUII Ul SctptOpel ,-.
Same 5.5
(80% value according to calcu- 4.0
lation method as with the case 0
of the amount leached).
DO concentration corresponding
to 100% DO saturation. Tokyo 8.0
Bay, summer: 7.5-8.5 ppm) ppm
Monthly value for the bay
from results of water quality 1.0
measurements in 1976. 0.08
Remarks
Calculated tide:   120 tidal
dilution coefficient:  1.0
                                       diffusion coefficient:   105 cnr/sec,
                                   112

-------
     In the surface  layer,  the values resemble the current values of 0.02 ppm
near the  mouth of  the  bay.   But,  the  current values from the middle  to the
innermost part of the bay are higher.

DO

     In the surface  layer,  the calculated values  for  the  whole  area are more
than 8 ppm.   Actual  measurements  show supersaturated areas of 7  ppm or over,
except in the  western  part of the bay.   However, in the substratum,  there are
wide-ranging oxygen-poor conditions,  especially  in the area on the east coast
of the inner  bay  where the calculated values were 4 ppm or less  and their low
values match  the  actual  measurements.   The 5 ppm isopleth at the mouth of the
bay closely resembles the current value.

Summary

     When the  above results  are  summarized,  it  is evident  that the model's
accuracy was  rather  poor  for COD in the  substratum and for P04-P in the sur-
face layer.  But  in  general  the calculated values  matched  the current values
quite well  from the mouth to the middle of the bay.
PREDICTION OF EFFECTS OF SAPROPEL REMOVAL

     The  following   two  cases were  considered  to  determine  the effects  of
removal of sapropel:

Case 1:   Removal of 75 km2 of sapropel for areas  in the bay with particu-
          larly high leaching  rates and oxygen consumption (Figure  22).

Case 2:   Removal of 400 km2 of sapropel from abiotic areas (Figure 22).

Figures  23 to  28  show the predicted changes in water quality for Cases 1  and
2.

     In Case  1  the  4 ppm and 5  ppm  predicted COD isopleths  in the  middle  of
the bay, when  compared with current conditions, would shift inside the bay in
the surface layer, as would the 3 ppm isopleth in the substratum.   The predic-
tion is, therefore,  that  Case 1  removal would  purify  the water in the inner-
most and  middle parts  of the bay.   The  P04-P  would  not change  much  in  the
surface layer  -  there  would be an improvement  of about 0.01 ppm in the inner
bay.  There would be few  differences for DO  in  the  surface layer, but in  the
substratum there  would be  fewer  areas of  4 ppm or less and  the oxygen con-
centration would increase  near the mouth of the bay.

     In Case  2,  the  COD  concentration would  decrease  by 0.5-1.0  ppm from  the
middle  to  the  innermost  part  of  the  bay,  and  there  would be  a remarkable
improvement in water quality.   The P04-P would show small values in the inner-
most part of  the  bay with large decreases  in the substratum.   There would be
almost no change  in  the  DO in the surface  layer, but in the substratum there
would be an increase  in the oxygen concentration of about 1 ppm.


                                     113

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                          0510 km

                     HIGHLY POLLUTED AREA (CASE I)
                     ABIOTIC AREA (CASE 2)
                     DIVISION BY BLOCKS
Figure 22.  Critical  areas  for sapropel  removal
                  114

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115

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117

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118

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119

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120

-------
     Article 9  of the  Basic  Law  for  Environmental  Pollution  Control  (1967)
sets standards  intended  to develop and maintain water quality in public water
areas with respect to the  protection of human health and the environment.  The
health standards  are  uniform  for all areas, but those concerning the environ-
ment  include  different  standards  for  various  types  of water  areas,  such as
rivers,  lakes  and the  sea,  depending on  the purpose for which  the water is
used.  By categorizing  aquatic  areas by use, the  environmental  quality stan-
dards for a  critical  area are clearly indicated.  In Tokyo Bay, the water use
categories for 18 regions are shown in Figure 29.

     Table 3 shows the environmental quality standards for COD with  respect to
present  conditions  and the Case 1  and Case 2 predictions.  The results indi-
cate that, at present, the standards have been  achieved for about 61% of Tokyo
Bay  as  a whole.  Among  the various types  of areas, the B type showed a  par-
ticularly low  achievement ratio of  about 36%.   For  the simulated cases where
the  sapropel  is  removed,  the improvement  is naturally  much  greater when the
removal  area  is larger.   In Case  2  where 400 km2  of sapropel is to  be  removed
from  the abiotic zones, it is  difficult  to achieve the required standards in
more than 75% of  the  B category  areas, but  the  percentage  rises to 77%  for the
whole  bay and  such  an  improvement can  be  expected  to create  a fairly  good
aquatic  environment.
  TABLE 3.  ENVIRONMENTAL QUALITY STANDARDS AND ACHIEVEMENT RATES (Unit:  %).
Item                                              COD
Use Category	A	B	C	Whole Bay

Standard values        2 ppm or less    3 ppm or less   8 ppm or less

Current values              78.4             35.7            82.9        61.4
removal (Case 1)
400 km2 of saprcpel
removal (Case 2)
78.4
89.2
38.9
60.3
82.9
87.8
62.7
77.1

IMPLICATIONS OF MODEL RESULTS FOR THE BENTHOS

     Figure 30  shows the  relationship between the benthos  and  COD,  sulfides,
and  ignition  loss in  bottom  deposits.   It  is  the  same  as Figure  12  but is
marked with the predicted values from the simulation.  The removal of sapropel
improved ignition loss to 7%, sulfides to 0.2 mg/g and COD to 13 mg/g.  It can
be assumed that the  number  of organisms and the species diversity will  there-
fore increase.


                                      121

-------
           TOKYO
          KAWASAKI
        YOKOHAMA
                                        CHIBA
                                         ICHIHARA
                                     KISARAZU
                     Bn
              YOKOSUKA
Utilization Category
TOKYO BAY 1 Conservation of environment
2
3
4
5
6
7
8
9
10 Fishery, class 2: industrial
water and uses listed in C
11
12
13
14
15
16
17 Fishery, class 1; bathing;
conservation of natural environ-
ment and uses listed B, C
18
Category
C
C
C
C
C
C
C
C
C
B

B
B
B
B
B
B
A


A
Figure 29.   Area ranked by environmental standards

                            122

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                                      123

-------
     Figure 31 shows the relation between the benthos and water quality.  At a
DO concentration of 5 ppm,  the number of species decreased to five or less and
at about 3  ppm,  the organisms numbered five or less.  Since an increase in DO
concentration  in  the  substratum is  one of  the  anticipated effects  of  the
removal of  sapropel,  there  should be a correspondingly better environment for
organisms with  improvement  of bottom  deposits and  water  quality.   This will
have a  major effect  on  the  recovery  of  marine life as outlined by the flow
diagram in  Figure 32.

                                  CONCLUSION

     Through studies of bottom deposits, water quality and biota in Tokyo Bay,
it has  become clear  that sapropel,  which has accumulated widely  in the bay,
has a major  deleterious influence on  the water quality and biota.

     A  mathematical  eutrophication  model  was  developed  to  investigate  the
effects of  the  removal  of  sapropel  on water quality.  The model was construc-
ted based on  data  from experiments  on leaching of organic detritus and nutri-
ents from the  deposits  and  DO consumption by the deposits.  The results indi-
cated that water quality would be greatly improved by the removal  of sapropel,
especially in the middle of the bay.

     However,  many  questions still  remain  unanswered;  among  them are  the
long-term  accumulation,  decomposition  rates   and  formation  of new sapropel
deposits after  removal.   This  research  will  therefore  be  continued  in  the
future.
                                     124

-------
                  REMOVE ACCUMULATED POLLUTED SLUDGE
                  REDUCE SIZE OF LOW OXYGEN REGIONS
        FACILITATE DECOMPOSITION OF DETRITUS, PREVENT NUTRIENT
        RELEASE, STABILIZE TOXIC SUBSTANCES
                                 ฑ
        PREVENT RED TIDE BY DECREASE OF SECONDARY POLLUTION
            PREVENT LOW DIVERSITY BENTHIC COMMUNITIES
            REDUCE WATER POLLUTION BY DECREASE OF COD,
            TOC, NX AND Px AND INCREASE OF DO
RE-ESTABLISHMENT


OF A


VIABLE


LIVING

COMMUNITY
                      INCREASE IN  FISHING    (MIGRATION OF FISHES...
                                          SAUREL, GRAY MULLET, SPRAT)
INCREASE OF BENTHOS  (BIVALVES.. .SHORT NECKED CLAM,
                     ARK SHELL, FLATFISH, YOUNG
                     SEA BASS, GIANT CLAM)
INCREASE OF
ZOOPLANKTON
                      DECREASE OF
                      PHYTOPLANKTON
(CRUSTACEAN)
                    (DECREASE OF RED TIDE)
                   - DECREASE OF ABIOTIC    (MULTIPLICATION OF
                     ZONE                SLUDGEWORMS)
Figure  32.  Flow chart showing effects of improved bottom deposits in Tokyo
           Bay.
                                 125

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                   RELEASE OF NUTRIENTS FROM LAKE SEDIMENTS
                              Ken Murakami, Chief
                      Kiyoshi Hasegawa, Research Engineer
                             Water Quality Section
                       Public Works Research Institute,
                       Ministry of Construction, Japan
                                   ABSTRACT

     Laboratory experiments  were conducted  on  the  release  of  nutrients from
bottom sediments under various conditions.  The relationships between nutrient
release rates  and  nutrient  content of sediments, temperature, redox potential
of  overlying  water and other  factors  are discussed, based  on  the  results  of
the experiments.

                                 INTRODUCTION

     In  recent years,  eutrophication has  become a  serious problem  in many
major lakes and reservoirs  in Japan including Lake Kasumigaura, Lake Suwa and
Lake  Biwa.    The  phytoplankton  blooms  accompanying  eutrophication not only
obstruct  direct water utilization,  but  scenic spots that used  to  have beau-
tiful  crystal  clear  water  have lost  their  recreational value.  The  primary
reason for eutrophication  is the increase in nutrient loading from the drain-
age  basin of   each  lake.   But it  is  also well  known that  nutrient exchange
between bottom sediments  and overlying water is strongly related to increased
eutrophication.  Much research has been conducted on the role played by bottom
sediments as  a nutrient storehouse.   However, the rates  of  nutrient transfer
between the two phases  have not been  fully  quantified.   This makes it diffi-
cult to  accurately estimate  the nutrient budget  of lakes,   particularly  for
short time periods.

     Laboratory experiments  on  the  release of nutrients from bottom sediments
used  both disturbed  samples  and  undisturbed  core  samples with  flocculant
sediments on  the  surface.   The  result of the experiments is  discussed in this
report.
                              EXPERIMENTAL METHOD

EXPERIMENTS USING DISTURBED SAMPLES

     Both continuous and  batch  experiments were carried out using the appara-
tus  shown  in Figure  1.   The vessel  is  60 cm high and 40  cm  inside diameter
with a capacity of 75 liters.  Tests were conducted by filling the bottom with
a sediment  layer  approximately  10 cm high.  In the batch apparatus a magnetic

                                     127

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           SATCH TYPE

           II	l|	
                                    DISTILLED
                                     WATER
   CONTINUOUS TYPE

             II	II
                                            CONSTANT
                                            FEED PUMP
                   SEDIMENT!
           I      \
        Figure 1.   Apparatus  for experiments  with  disturbed  samples.
stirrer was used to  examine  the effect of the  velocity  of  the  overlying  water
on the release of  nutrients.   Distilled  water  was  used  as  the  overlying  water
in both batch and continuous systems.

     In the batch  test,  the  gas phase was released to  the atmosphere  in test
runs under  aerobic conditions.   In test runs  requiring anaerobic  conditions,
the water  was  purged by  nitrogen gas  and,  at the  same  time, the gas  phase
(air) was  replaced  by nitrogen prior to  the tests.

     The  continuous tests were  performed to  observe the variation  in  release
rates when the  overlying water of the bottom  sediments changed  from aerobic  to
anaerobic, and from  anaerobic  back to aerobic.  To change  the  test water from
aerobic to anaerobic, distilled  water  free from dissolved  oxygen  was  supplied
while,  simultaneously the water in the vessel was purged with nitrogen.

     The   bottom  sediment samples  used in  the  tests were  collected from Lake
Kasumigaura,  Lake Teganuma,  Lake Toyanogata and the outer moat  of  the  Imperial
palace in Tokyo.   Some  sediment  samples  taken  from the bottom  of  the  Anakawa
River and  the Tsurumi River were also  used.
EXPERIMENTS USING UNDISTURBED SAMPLES

     Flucculant  sediments  on  the  lakebed
release of  nutrients  by bottom  sediments.
are  difficult  to  collect  by conventional
taken  using core  samplers,  and  the  core
apparatus.
surface  could be  related  to  the
 Since  these flocculant sediments
methods, undisturbed  samples were
tube  itself  was  used  as  a test
                                     128

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     As  shown  in Figure 2,  the  sampler consisted of  an  acrylic  plastic tube
with an  inside  diameter of 5.2 cm and  a length of about 66 cm.  A sufficient
number of  samples were collected at  a  single station to provide  5 tubes for
each test  run.   The  samples  were  returned to the laboratory  where the over-
lying  water  was  carefully replaced  by lake water  filtered  through  a 0.45(j
membrane filter.
                                         AIR RELEASE HOLE
                                         ACRYL CORE
                                         SAMPLER
    Figure 2.  Core sampling for experiments requiring undisturbed samples.

In this experiment, since water volume in the core tubes was small, five tubes
of samples were  run simultaneously and used as replicates.

     For  the experiments  under aerobic  conditions,  the overlying  water  was
continuously aerated by a small amount of air during the test period.  For the
experiments  under  anaerobic conditions,  two   modifications  were  made.   The
first was  to remove  dissolved oxygen in the overlying water by using a nitro-
gen gas purge.  The  second  was  to add glucose  to the water (20 mg/1 at 20ฐC)
after  removing  the  dissolved  oxygen.   This   helped  maintain the  anaerobic
state.

     The bottom  sediments used in these tests were  collected from Lake Kasumi-
gaura.   The  sampling stations are  shown in Figure  3.  An  attempt was made to
maintain a consistent  thickness of bottom  sediments for each sample.  But, in
practice,   they  varied  in  thickness  from  10  cm  to  32 cm with an average of
about 20 cm.
                                      129

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                                                                       10 km
       Figure 3.   Sampling stations (core samples)  in Lake Kasumigaura.
                            RESULTS AND DISCUSSIONS
PHOSPHORUS RELEASE

(1)  The  relationship  between  phosphorus release rate  under  anaerobic condi-
tions and phosphorus content of the sediments.

     The  release of  phosphorus  from bottom sediments  increases  markedly when
dissolved  oxygen  in  water and  the oxidation-reduction potential  decreases.
Figure  4  shows  an example  of  results  obtained  from  a  continuous-type test
with  a  disturbed  sample.   It  is  clear  from the  figure  that the  phosphorus
concentration  in  the  water  begins  to increase  as  the concentration  of dis-
solved oxygen decreases.  However, the release rate after  the dissolved oxygen
reaches  zero is not  constant.   Figure 5  shows the time variation of the phos-
phorus release rate as  calculated from the data  shown  in  Figure 4.  The gen-
eral pattern is that,  immediately after  reaching an  anaerobic condition,  the
release   rate  shows a marked increase  and  then decreases  after  about  6 days.
The  phosphorus  release  rate  under anaerobic  conditions  is, therefore,  time
dependent.  The average  release  rate  during the first one-  or two-week period
after the dissolved  oxygen  declined  to  zero  was compared  to the  phosphorus
content   of sediments,  as  shown  in Figure  6.   The release  rate was  in pro-
portion  to the phosphorus  content of the sediments, and could be approximated
by the following equation
               Y = 10X
(1)
                                      130

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       0


      04
    O>
    8
     .-02
                                       -Fe
                        10       15      20
                            TtME, DAYS
25      30
Figure 4.   Variation of quality  of  overlying water;  continuous
           type experiment with  Lake  Teganuma sediments.
                             131

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            30 r-
           -20 u
Figure 5.  Time variation of phosphorus release rate;  continuous  type
           experiment with Lake Teganuma  sediments.
                  100
              UJ
              <

              ""
                 ESO
              K
              O
              O
              X
              a.
                                              O
                            J
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                            2468
                       PHOSPHORUS CONTENT OF SEDIMENTS
                            P-mg/g DRY SO LIDS
      10
Figure 6.   Relationship between phosphorus release rate under anaerobic
           conditions and phosphorus content of sediments; experiments
           with disturbed samples at 20ฐC.
                                     132

-------
where, Y  is  the average release
conditions at  20ฐC  and X is the
solids).
rate of phosphorus (mg/m2/day) under anerobic
phosphorus content of the sediments (mg/g dry
     The  same  relationship was  obtained  by  experiments  using  undisturbed
samples  with  flocculant sediments.   Figure  7 shows  the  relationship between
the average release rates during the first 11 days after the start of the test
at  20ฐC,  and the  phosphorus  content of the  surface  sediments.   It  is inter-
esting  that  equation  (1)   is  also  a good  approximation for  the  flocculant
sediments.
                 10
                  8
            LU

            S
            cr
            m
            Jr
            o
            CO
            i
            Q.
                             I         I         I
                         • ANAEROBIC (Glucose Addition)
                         C ANAEROBIC
                         O AEROBIC
                                                     €
       $
                                    O
                                                     O
                                      1
                            0.2       0.4       0.6        0.8
                          PHOSPHORUS CONTENT OF SEDIMENTS
                                 P-mg/g DRY SOLIDS
                                 1.0
        Figure 7.   Relationship between phosphorus release rate and phosphorus
                   content of sediments; experiments with undisturbed samples
                   at 20ฐC.

          The pattern of  time  variation  of phosphorus release under anaerobic
conditions,  particularly  the  fast rate  immediately  after conditions  become
anaerobic, suggests  that  reduction of  ferric phosphate  is  significantly  in-
volved in  phosphorus  release from the sediments.  As  shown in Figure 8, there
is a good  correlation between phosphorus and iron  in the overlying water.
                                     133

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            0.20
            0.16



          E
          o. 0.12

          of
          o
          .c
          ฐ o:os
            0.04
                  12
                       0.2      04       0.6       0.8
                                    Fe~, T-Fe,  mg/l
                                                          1.0
                                                    1.2
     Figure 8.   Relationship between phosphorus and iron in overlying water;
                continuous type experiments with  Lake Teganuma sediments.
(2)  The  relationship  between  the  release  rate  and the  level  of dissolved
oxygen in overlying water.

     As  mentioned  previously, phosphorus  release from  bottom sediments is  a
function of dissolved oxygen in the overlying water or a function of oxidation-

reduction  potential.  Even   though  dissolved  oxygen  or  oxidation-reduction
potential  is constant, the phosphorus release  rate  is time dependent.   There-
fore, it  is  difficult  to find a  strict  relationship between  the release rate
and the  dissolved  oxygen level.   A rough relationship was  obtained based on  a
large number of data from the batch-type test using  disturbed  samples.   Figure
9  is  the  result  of  this  analysis,  showing the  relationship between  release
rate (at  20ฐC)  and phosphorus content of  the  sediments for varying dissolved
oxygen regimes  in  the  water.   The release rate may  be expressed similarly  to.
equation (1), i.e.
where Y and  X
coefficient "a
 Y = aX

 in  equation (2) are the  same  as in equation (1).
'  is roughly within the  range  shown in Table 1.
                                                                 (2)
                                                                  The  value  of
                                      134

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                                      1:10
9 r
                                              Ka  LAKE KASUMIGAURA
                                              To  LAKE TOYAN06ATA
                                              Tega: LAKE TEGANUMA
                                              Ara. ARA RIVER
                                                           13
                                                       1.2 2
                                             O Ka. 24 (o*Do
-------
               TABLE 1.   EFFECT OF DO LEVEL ON PHOSPHORUS RELEASE RATE



                            Range of DO           Coefficient a


                            0 mg/L                a >  10

                            0 -v 0.5 mg/L          10 > a > 3

                            0.5 ^ 1.0 mg/L        3 >  a > 2.2

                            > 1.0 mg/L            2.2  > a
 (3)  The relationship between the release rate and water temperature


     From the fact that  the  phosphorus content in water increases markedly in
shallow lakes during the  summer,  it is assumed that water  temperature greatly
influences   the   release  rate of  phosphorus.   Experiments  using  undisturbed
samples were  performed  at 10ฐC,  20ฐC  and 30ฐC.   The results of  plotting the
average release  rate for  the first  11  days  of the test against  water tempera-
ture are  shown  in  Figure  10.   Under  anaerobic  conditions  the  release  rate
averaged 2.6  times higher  at 30ฐC than at 20ฐC.   The effect  of  water tempera-
ture on release rate is expressed in  the following equation.
                              YT = Y20ฐC 6  "


where the coefficient 0 between 20ฐC  and 30ฐC is 1.08.
     Although fewer data are available for the 10-20ฐC temperature conditions,
they imply 0 = 1.05 for both aerobic and anaerobic conditions between 10ฐC and
20ฐC.
                                      136

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            20
         UJ
         IT

         UJ
             15
             10
         o
         i
         a.
O
C
o
n
o
n

O
O
             I
ST. 1 AEROBIC
ST. 1 ANAEROBIC
ST. 1 ANAEROBIC (Glucose Addition)
ST 2 AEROBIC
ST 2 ANAEROBIC
ST. 2 ANAEROBIC (Glucose Addition)
ST. 3 ANAEROBIC
ST. 4 AEROBJC
ST. 4 ANAEROBIC
                                                   D
                                  10                  20
                                   TEMPERATURE, ฐC
                                                      30
     Figure 10.   Effect of temperature on phosphorus release rate;  experiments
                 with undisturbed samples.
(4)  Other factors influencing release rate

     Other physical  and chemical factors  related  to  the release rate of phos-
phorus are the  velocity of the  overlying water and  the diffusion coefficient
in the sediments.   When comparisions were  made  using the batch-type tests for
release rates,  with and without being  subjected to water  flow,  there were no
significant  differences observed.   This  is  because the majority  of  the tests
were  conducted  under anaerobic  conditions  and  the release of  phosphorus was
predominantly caused by the reduction of  ferric  phosphate rather than physical
diffusion.  The release under aerobic conditions  and the steady release under
long  term continuing anaerobic  conditions  may be  significantly  influenced by
the  velocity of  the water.   No  detailed  studies were  made  on porosity or
diffusion  in  the  bottom sediments,  but there  is probably an influence similar
to that of water velocity.

     In addition,  the  release rate  when  flocculants  were  present  on the sur-
face of the sediment, showed  virtually  no differences compared  to when floccu-
lants  were  not present,  based  on  data  gathered  under  anaerobic  conditions
(Figures   6 and  7).   Since few tests  were run with flocculant  sediments under
aerobic conditions, no  comparison  of these  results  could be made  with those
obtained  under  anerobic conditions.  Further  studies on this subject will be
made.
                                      137

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RELEASE OF NITROGEN
(1)  The  relationship  between  the  release  rate of nitrogen  and the nitrogen
content  of  the  bottom  sediments,   and   between   the  release  rates  and the
oxidation-reduction potential of the overlying water.
     The mechanism of nitrogen  release  from the
less time-dependent  than
                                    bottom
                                    Tun  f.
                                         sediments
                                                                  is considered
                           that of  phosphorus.   Two factors  are considered  to
control the release  rate.  One is  the  decomposition of particulate nitrogen  to
dissolved  nitrogen  in  the sediments,  and  the  other is the  diffusion of  dis-
solved  nitrogen  into the  overlying water.   Similar to  phosphorus,  major  fac-
tors influencing  breakdown of  nitrogen  will  be the total  nitrogen content  of
the  sediments,  aerobic-anaerobic  condition of  the overlying  water,  and  tem-
perature.

     From  the  results  of  experiments  made  at 20ฐC  water  temperature, corres-
ponding values for nitrogen  release rate and  nitrogen  content of the  sediments
were found  for  both aerobic  and  anaerobic  conditions.  The  results  are  shown
in  Figure   11.   Under  either  aerobic  or  anaerobic conditions,  the  nitrogen
                    100
                    80
UJ

cr
UJ
               Z  E
               UJ
               CD  Z
               O  i
                    60
        40
                    20
                    I          I         I
              O UNDISTURBED SAMPLES, Aerobic

              O UNDISTURBED SAMPLES, Anaerobic

              • UNDISTURBED SAMPLES, Anaerobic
                  (Glucose Addition)

              D DISTURBED SAMPLES, Batch Type
                  Experiment, Aerobic

              A DISTURBED SAMPLES, Continuous
                  Type Experiment, Anaerobic
                                            a  -
                         €>
                         a

                         o
                         D
                                 0
                              1
                                      a

                                     a
                              a        a

                                n


                              	i
Figure 11.
          02468
             NITROGEN CONTENT OF SEDIMENTS,
                  T-N mg/g DRY  SOLfDS
Relationship between nitrogen release  rate  and nitrogen
content of sediments (20ฐC).
                                      138

-------
release rate  is roughly  proportional to  the nitrogen  content of  the  bottom
sediments.  However, under  anaerobic conditions the  nitrogen  release rate was
about 2 to  3  times greater  than  under aerobic conditions.  The  only possible
reason  for  this  is that  the rate  of decomposition  of particulate  nitrogen
under anaerobic conditions  is  much  higher  than under aerobic conditions.  This
is an  interesting  result.   The  effect  of flocculant  sediment was  not great
since data from both disturbed  and undisturbed samples show a similar trend.


(2)  The relationship between nitrogen release rate and water temperature.

     Similar  to phosphorus, when  plotting the  average nitrogen  release rate
for  the  first  11  days of the water temperature experiments  with undisturbed
samples,  the   relationship   shown  in  Figure  12 was  obtained.   The  effect of
water temperature  on  the nitrogen  release rate was great.  The  release rates
at 30ฐC under anaerobic conditions  were about twice those  at 20ฐC.  Assuming
the  same  relationship  as  equation  (3)  for  the  effect of temperature  on the
nitrogen release rate,  the temperature coefficient  6 was 1.07  between 20ฐC and
30ฐC  under  anaerobic  conditions.   Data for  10ฐC  to 20ฐC  under  anaerobic and
aerobic conditions  were limited and  therefore are  less  reliable,  however, they
were 1.06 and  1.095, respectively.
              80
              60
              20
            I                ]
O  ST. 1 AEROBIC
O  ST. 1 ANAEROBIC
•  ST. 1 ANAEROBIC (Glucose Addition)
D  ST. 2 AEROBIC
B  ST. 2 ANAEROBIC
•  ST. 2 ANAEROBIC (Glucose Addition)
1^  ST.  3 ANAEROBIC
O  ST. 4 AEROBIC              C>
^>  ST 4 ANAEROBIC

                           •O
                                O
                               _l	

                                                              D
                                10              20

                                  TEMPERATURE, ฐC
                                           30
     Figure 12.  Effect of temperature on nitrogen release rate; experiments
                 with undisturbed samples.
                                      139

-------
(3)  The qualitative effect of water velocity on nitrogen release rate.


     When  comparing the  nitrogen  release  rate  with  the phosphorus  release
rate, the  nitrogen  release was considered  a  more stable  phenomenon,  and thus
more affected  by  diffusion.   From the results  of bottom tests employing dis-
turbed samples, the qualitative effect of  water  flow on  nitrogen  release was
examined.  Comparison  of the  release rates with  and without water flow over
the  sediment  surface  is  shown  in  Figure  13.  According  to Figure  13,  although
the  data show quite a  spread,  the nitrogen  release  under conditions  of flov*
was  larger than that without flow  for  about  80% of  the data.   Since  rotation
of  the  magnetic  stirrer  imparting velocity to the  overlying water was  arbi-
trarily  controlled, it  was  impossible   to  express  the  effects  of  velocity
quantitatively.
                                                 1:2
                                                         1:0.6
                                                O AEROBIC
                                                • ANAEROBIC
                                   0.5      10       15
                                NITROGEN IN OVERLYING WATER
                                WITHOUT VELOCITY, T-N g/m*

                Figure 13.  Effect of velocity on nitrogen release.
                                      140

-------
                                  CONCLUSION

     After  careful  examination  of  the test  results for  both  phosphorus and
nitrogen release from the bottom sediments of  lakes, the following conclusions
can be made:

   (1)  Phosphorus release

     (a)  The major factors  that control  the phosphorus release from sediment
are the  phosphorus  content  of  the  bottom sediments, the  DO  in the  overlying
water,  and  the temperature.

     (b)  Although the  phosphorus  release rate  under  anaerobic conditions is
not constant, the average release rate during the first one or two weeks after
the overlying  water  becomes anaerobic  is  in proportion  to  the  phosphorus
content, of  the bottom sediments.  This relationship holds even when flocculant
sediments are present on  the surface.

     (c)  The phosphorus release rate is small under aerobic conditions in the
water.   When  dissolved  oxygen  was  over  1  mg/1,   the  rate dropped  to about
one-fourth  of that  under anaerobic  conditions, based  on  results  from experi-
ments  using disturbed samples.

     (d)  The phosphorus release rate  is  greatly  influenced  by temperature.
Under anaerobic  conditions,  the release rate  at 30ฐC  is  more than twice that
at 20ฐC.


(2) Nitrogen release

     (a)  Similar to  phosphorus,  the  nitrogen  release  rate   depends  on the
nitrogen content of the  bottom sediments, the DO  of the overlying water, and
the temperature.  It is  also affected to a  certain extent by the velocity of
the overlying water.

     (b)  Under  both  anaerobic and  aerobic  conditions, the  nitrogen release
rate is roughly  proportional  to the nitrogen content of the bottom sediments.
But, the release  rate  under anaerobic conditions is two or three times higher
than under  aerobic conditions.

     (c)  The nitrogen  release rate,  similar to phosphorus,  is  also greatly
influenced  by  temperature.    The rate  at 0ฐC under anaerobic  conditions is
about twice that  at 20ฐC.

     Some  of the above  conclusions  are tentative.   More  studies  are required
to  probe  the  release  of  nutrients  from  bottom sediments,  especially under
aerobic conditions,  and to elucidate the influence of temperature.


                                ACKNOWLEDGEMENT
     The  experiments  using  undisturbed  samples  were  performed  by  the  Lake
Kasumigaura  District  Office  of the  Ministry of Construction.   Gratitude  is
expressed to those conducting the experiments.

                                      141

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                   TEST RESULTS FROM DEMONSTRATION DREDGING
                    AND SPILLWATER TREATMENT AT HIRO HARBOR
                              Toshihiko Fukushima
                    Construction Bureau,  Kure City Office

                                Tathuo Yoshida
                 Japan Bottom Sediments Management Association


                                 INTRODUCTION

     Hiro Harbor  is located  in  the  Hiro section of Kure-shi, a  coastal  city
near Hiroshima.  Formerly  a  small  fishing village, Hiro became a major indus-
trial  import  and shipping facility  after Toyo  Pulp Industries  Ltd.  built a
large  kraft paper mill  on  its waterfront.  The  wastewater  from  the mill  pol-
luted  the area  for  a long time and,  as a result, large quantities of polluted
sediment now cover the harbor floor.

     To deal with this pollution problem, the Kure-shi  Municipal  Office set up
a pollution control  committee for  Hiro Harbor which has  formulated a plan to
clean up the area.   This plan requires the dredging of  200,000 cubic meters of
sediment, which will then be  used as  fill for a land reclamation project.


     The implementation of this project, requires the consent of the residents,
particularly  the  fishermen,  because  of  their concern  over  the  environmental
impact  of  the operation.  The  demonstration discussed  here was  designed to
help  obtain  this  consent  and  to  determine  probable  environmental  effects.

     In  early June  of  1978,  about 900 cubic meters of  sediment  were dredged
for  demonstration  purposes.   Ancillary tests on  spillwater  treatment,  sludge
solidification, and  bioassay  techniques  were conducted.  Results are reported
in this paper.
                              OPERATIONAL METHOD

     The dredging  operation was  performed  as shown in Figure  1.*   A special
antipollution  suction  dredge dumped  the  dredged material  into  a  barge.   The
barge was  then anchored  to the  wharf  near the  experimental  water treatment
plant.    The  material  in the  barge  was  allowed to  settle naturally  over  a
two-day period.  During this time the mixture separated into clean supernatant
 * Figures and  tables  for this paper are found at the end of the text, begin-
ning on page 147.


                                     143

-------
water and  precipitated sludge.   The  water was pumped to  the  water treatment
plant, and  the sludge,  after  solidification,  was  hauled  to a  dump  pit.   It
took only one  hour  to dredge the sediment, but about 10  days were required to
treat the spillwater because of the small  capacity of the test plant.

     This public  demonstration of sediment management was  worthwhile because
it increased the  general  public's understanding of the  plan  to  clean up Hiro
Harbor.

TURBIDITY

     Turbidity generated  by  dredging  is one of the most  difficult problems to
deal  with.   To control  turbidity,  several unique  suction devices have  been
developed in  Japan.   In  Hiro  Harbor,  one  of  these devices was  used.   It is
similar to the one shown in Figure 2.

     Two sets  of  augers  with  opposite pitches  are mounted on  a common  axis
within the  suction  device.   The rotation of the  screw forces  the sediment to
move to  the center  where it  is  picked up and  pumped  to  the  surface.   When
dredging with  such  a device, turbidity is  kept  low because of the smoothness
of the cut  and the  near-perfect removal of loosened sediment particles.   This
is in contrast to conventional  cutter-type devices.

     Observations of turbidity were made during the Hiro  Harbor demonstration.
Measurements of SS  concentration  and  the degree  of  turbidity  were taken at 9
stations in  the  area,  which was a  square 100  m on a  side beginning  at the
dredge site  and  running  100 m in  the direction of  diffusion.   Samples  were
taken at three depths at each station.  The results  are summarized in Figure
4.

     The maximum  SS  concentration near the dredge was 6  ppm.   We estimate the
increased concentration  due to  dredging  as only  1-2 ppm  by  subtracting the
background  level  of  SS from the measured values.  Therefore, it appears there
is virtually  no  turbidity  created  by dredging with  this  equipment under the
existing  conditions.   Similarly,  the  maximum  degree of  turbidity  was  only
0.6ฐ.

     The demonstration dredging statistics are:

               swing width                        50 m
               swing speed                        4 m/min
               thickness of sediment              1.2m
               thickness of cut                   0.4 m
               amount of dredged sediment         130-180 m3/hr
               percent solids                     20-40%
               dredged water                      650 m3/hr

     The  sediment  thickness  and pulpy  quality resulted  in easy dredging.

SEDIMENT PROPERTIES

     Four  samples were examined  to determine the  particulate composition of
the  sediment.


                                      144

-------
Locations of sampling
stations
     Table 1 shows  that  the grain size of the sediment at Hiro Harbor is very
small—over 60%  of particles are  under  6.8 M.   This  is  smaller  than results
suggested by laboratory  tests  last year which gave a D60 of 12 p and a D30 of
2.4 (j.

     Physical  and  chemical  properties  of the sediments obtained last year are
given  in  Table  2.  The  level  of  toxic  substances  is  negligible  except that
comparatively high  contents of  Pb (20  ppm),  Zn (349 ppm) and  As  (5.81 ppm)
should be watched.

     Organic matter content  is  fairly  high as indicated  by the high COD con-
tent—the highest  we  have  ever  seen (Table 3).  This  may be due to the pulpy
nature of the sediment.   The content of the n-Hexane extractions is also high.
This means that  the sediment contains  large quantities of organically derived
oils.  The ammonia-nitrogen content is  unexpectedly small.  This may be due to
conversion of  sedimented nitrogen  components  to easily  dissipated ammonium.
The  high  hydrogen  sulfide  content  is  responsible for  the  bad odor  of  the
dredge water(Figure 5).

     The physical properties of the dredge water were analyzed and results are
given in Table 4.

     Data  in  Table  4 and  Figure  6  were  obtained from laboratory  tests  of
dredge  slurry  containing  10,  20,  30  and 40%  solids.   These data  show  the
relationship between  SS  and various chemical  and physical  variables.   Use of
these data with  field measured  SS concentrations provides  an  estimate of the
other  variables.   It  is extremely difficult to  measure these  variables  di-
rectly.

WATER TREATMENT

     A schematic  of the  water  treatment plant is  given  in  Figure 7.   It is a
demonstration plant which  was  set up to treat the  supernatant water from the
spoils barge after the  sediment had settled naturally in the barge hold (Fig-
ure 8).

     It took  45  hours to  obtain  a  1.8  m  depth of clean  supernatant water.
From this, the mean settling velocity can be calculated as follows:

                   W = 1.8 ^ 45 = 0.04 m/hr = 0.0011 cm/sec                (1)

     The  plant  was operated continuously  for 8  hours a day.   A circulating
high-speed vertical type filter  was used.   Sodium  hypochlorite,  a  food addi-
tive, was used  for chlorination.   A commercial  product  (Kurifloc  PA-331)  was
                                     145

-------
used  as  a  polymeric coagulant.   Table  5 shows  the additives  and  operating
parameters for the system.

     A precipitation test  was  carried out using a  1000  cc  cylinder.   Results
with and without  a  coagulant added are shown  in  Figure  9.   The mean settling
velocity without coagulation was

          W = (165 cm - 140 cm) •=- 6 hr = 0.042 m/hr = 0.0011  cm/sec,        (2)

which  agrees  with  the first  value  derived  from  measurements in the  barge.
These  slow  settling rates  will  cause difficulty in handling  the  Hiro  Harbor
sediments.   The  SS  concentration  in  the supernatant  water  was 30-60  ppm by
weight.

     Table 6  shows  the water quality at each stage of operation.  The initial
SS  concentration  was  reduced  to  8-12 ppm  after coagulation,  and to  1-5 ppm
after  filtration.   From  the data presented in the  table,  it can be  seen that
COD.,   concentration and the total phosphorus  concentration were reduced in
proportion to the SS removed.  This is illustrated in Figure 10.

     Since the guidelines  for  discharging this kind of water are generally 30
ppm SS and  20 ppm COD.,  the water remaining after coagulation of the sediment
might  have been  clean  enough to discharge.   However the T-N concentration was
too high.   Its  value did not drop at all  until the filtration stage, although
the SS concentration was  already reduced.  Only in  the  last stage,  when sub-
jected to chlorination  with sodium hypochlorite, did it drop adequately (Fig-
ure 11).

     The results of the chlorination test are shown in Figure 12.  The concen-
tration of NH4-N decreased rapidly as the active concentration of chloride ion
exceeded 150  ppm,  reaching a low point near  200-230 ppm of chloride ion.  At
the zero level the minimum residual chloride became noticeable.

     In the experimental operation,  the effect of  activated  carbon  powder on
the  reduction of SS and COD,,   at each stage was also examined.   The results
are summarized  in  Table 7.  it was  found that activated carbon powder has no
effect on the efficacy of the other processes.

     From  the above  results,   it  is  concluded  that the greatest problem in
supernatant water  treatment is  the  exceedingly high content  of NH4-N  in the
dredge water.   It  appears  that this concentration derives from bacteria which
convert the organic matter in the sediment into ammonium ion, and the ammonium
ion then dissolves  in  the  interstitial water  of  the sediment.  Since concen-
trated ammonium ion is toxic to fish, it  is necessary to reduce it below toxic
levels.  For  this purpose chlorination is required.   Usually the guideline for
water  quality when discharging  dredge water  is concerned with two  items—SS
concentration and COD.   But in the case  of  Hiro Harbor, NH4 must be added to
the guideline.

SOLIDIFICATION OF SLUDGE

     The sludge, which settled on the bottom of the barge, was not discharged
in  an  untreated state.   It was  solidified at the site and then  hauled by  truck


                                      146

-------
to  a  dump  site.   The  commercial  compound  "Chemikolime 235"  was  used as  a
solidifier.   This was combined with the sludge as follows:

Batch:
C-235
500 kg
Water
400 kg
C/Water
80%
Concentration
0.89 t/m3
     Since 85  m3  of solidifier were used  to  treat 490 m3 of  sludge,  the mix
percentage was  16.5%.   The  solidifier  was mixed into  the  sludge with a clam-
shell bucket.   The  compression  strengths of the solidified sludge are plotted
in Figure 13.  The deeper layer is stronger than the shallow one.  This may be
due to precipitation of the solidifier.   Good agreement between the laboratory
test data and  on-site  tests are shown by  Figure  14.   The good results may be
attributed to  selection  of  the  proper  solidifier and thorough mixing with the
clamshell.
                                  CONCLUSIONS

     The results  of experiments  at  the dredging site and water  treatment at
Hiro Harbor  led to  the following conclusions.  Turbidity from  dredge  spoils,
which  is  the most  troublesome aspect  of  dredging, can  be  negligible  if an
anti-pollution dredge  with  a  special  suction device is used.   The most impor-
tant aspect  of water  treatment in this area  is  the exceedingly high ammonium
ion  content  in  the supernatant  dredge water.   To  reduce  it  to  permissible
levels chlorination is  the  best treatment but, carbon is necessary to absorb
the residual  chlorine.

     This  demonstration was  valuable  in increasing  public  awareness  of  en-
vironmental problems and providing a basis for understanding  the plan to clean
up Hiro Harbor.
                      TABLE  1.  GRAIN SIZE OF SEDIMENT
                   Station  1    Station 2    Station 3    Station 4      Mean
Maximum Size |j
Deo
D3o
2
8.4
3.6
0.84
6.9
4.0
0.42
6.7
3.2
0.84
5.3
2.1
1.03
6.8
3.2
                                     147

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                       TABLE 2.   PHYSICAL  AND  CHEMICAL  PROPERTIES OF THE  SEDIMENT
Soil property
  Color
                     Odor
                        pH
            H20



            KC1
                     Water Content Ratio
                     Water Content
                     Specific Weight
                     Liquid Limit
                     Plastic Limit
                     Plastic Index
                                                      Black and Sticky
                                                                            Rotten
                                                                             7.80
                                                                             7.58
                                                                           436.8
                                                                            81.4
                                                         2.572
Unit Weight
Grain Max
g/cm3
H
1. 106
105
                                                                             12
                                                                             2.4
                                                      286.3
                                                       130.7
                                                       155.6
Nutrients
Ignition Loss
                     COD
                        Mn
                     COD
                        Cr
                     Nitrogen
                                      T-N
                                      NH4-N
                                      N02-N
                                      NO,-N
                     T-P
                     Ca
                     Sulfide
                     n-Hexane Extracts
                                      mg/g
                                      mg/g
                                      mg/kg
                                      mg/kg
                                      mg/kg
                                      mg/kg
                                      mg/kg
                                      mg/kg
                                      mg/g
                                      mg/g
   37.6
  225
  448
6,290
    7.53
                                                                              3.22
                                                                              3.22
1 ,020
2,540
                                                                              2.28
                                                                             11.35
Toxic Substances
                     T-Hg
                     Alkyl  Hg
                     Pb
                     Zn
                     Cr
                     As
                     Cd
                     Cyanogen
                     Organic P
                     PCB
                                      mg/kg
                                      mg/kg
                                      mg/kg
                                      mg/kg
                                      mg/kg
                                      mg/kg
                                      mg/kg
                                      mg/kg
                                      mg/kg
                                      mg/kg
                                                                              0.286
                                                                            <  0.0005
                                                                            20.0
                                                                            34.9
                                                                              5.81
                                                                            <  1.0
                                                                              0.001
                                                                            <  0.0005
                                                148

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                 TABLE 3.   DREDGE WATER RETURN FLOW STANDARDS
         Property
  Value
     Reference
COD
n-Hexane Extracts
Hydrogen Sulfide
Total Nitrogen
Total Phosphorus
20 mg/g
3 mg/g
6700 ppm
625 ppm
88 ppm
JIS K0102
JIS K0102
Sewage Analysis
Sewage Analysis
JIS K0102

       TABLE 4.   PROPERTIES OF DREDGE WATER RETURN FLOWS (SUPERNATANT)
Property
                                   Concentration of Sediment in Dredge Slurry
10%
20%
30%
40%
pH
SS (ppm)
Turbidity (ppm)
Transparency (deg. )
Color (deg)
CODM (ppm)
T-N Cpprn)
T-P (ppm)
Sulfide (ppm)
7.1
17,400
9,250
< 1.0
52.0
2,160
67.2
28.1
112
7.1
29,800
16,700
< 1.0
67.5
4,050
143
43.1
265
7.0
52,600
27,800
< 1.0
86.3
8,500
285
59.8
395
6.9
83,900
46,000
< 1.0
110
15,600
582
85.5
677
                                     149

-------



















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        TABLE 6.   SUPERNATANT WATER QUALITIES AT EACH TREATMENT STAGE
                                              Stage
Property
                                                Chlorinated
Input Water  Coagulated Water  Filtrated Water     Water
pH                  7.1-8.0
Color (deg.)        500-800
Turbidity (deg.)     30-60
SS (ppm)             30-60
CODM  (ppm)          25-37
T-N fr>pm)            22-25
NH4-N (ppm)          20-25
T-P (ppm)           1.1-1.5
n-Hexane Extracts (ppm)
                      < 5
Residual C12 (ppm)    —
Chloramin (ppm)        —
Isolated C12 (ppm)    —
Residual Polymer (ppm)
                 6.8-7.5
                 50-150
                  8-12
                 10-40
                  9-13
                 23-24
                 22-23
                0.4-0.5

                  < 5
0
6.8-7.5
 20-70
  2-5
  1-5
  3-6
 22-24
 22-23
 13-0.14

  < 5
6.8-8.0
 20-40
  1-3
< 1-3
< 1-3
< 1-3
< 1-3
< 0.1

< 5

ND

ND
ND


< 0.1
ND = not detectable
                                     151

-------






















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-------
                                   EXPERIMENTAL WATER TREATMENT
                                                       PLANT
DREDGE
          BARGE
   BARGE          r
.   ^JDai
                                                       a
      Figure 1.  Schematic diagram of the experimental  operation.
                                      SUBLADDER
    DIRECTION OF SWING
                                        GAS SUCTION
xVV '-V'1; / \' , ^ ,"
                              SCREW
            Figure 2.  Screw-type or auger suction head,
                            153

-------
0 50m V 100m 2.8


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         CUTTER HEAD
                                                                    5.0
    Figure 4.   Distribution of SS due to dredging (ppm).
                                                  300
                                                             2.572
400
                                  CODUn  mg/g
                                    'Mn
Figure 5.   3-axis  plot showing  relationship of ignition loss, COD and unit
           weight  of sediment in  Hiro  Harbor.
                                     154

-------
     ppm

   100,000
    50,000
    10,000
     5,000
  z
  o
  Ul
  O
  Z
  o
  o

  OT
  CO
1,000
       500
       100
           t-  o
                           TURBIDITY
                           Mn
                    SULFIDE
                     I    III
                               ppm

                              1000
                               500
100
                                50
          0    10     20   30 40 50%

            SOLIDS IN DREDGE WATER
                                10
                                       I
                                                        T-P
              I    III
                                  0   10     20   30 40 50%

                                   SOLIDS IN DREDGE WATER
Figure 6.   Relationship between  concentration of various pollution
            components of dredge  water and sediment  content.
                                155

-------
HIGH-SPEED   LOW-SPEED
REACTION    MIXING TANK
TANK
                                                                   ADHESfON TANK
.' •' TANK'.'." •.' f; TANK'FOR •'!
 .FORPAC . '  |.  POLYMER/
                     SETTLING- . •  ' .'SLUDGE-'.SETTLING'  .''.'• '. •'FILTRATE .'f.  '
                     TANK'  •   •  • TANK '• TANK   '      '   •  TANK •  •  •  '  "
1 .'  '  TANK FOR ACTIVATED '.•••'•.•   '  •            '    •  •   TANK FDR  '
•  •  '  CARBON POWDER  •   .   .         .   •          '               NEUTRALIZATION
            Figure 7.   Schematic of  water treatment  plant.
          Figure 8.   Natural  sedimentation in  barge hold.
                                    156

-------
                    I     I    I    I     I    I     I
                               WITHOUT COAGULANT
                               WITH COAGULANT
                                      I     I
I    I     I
               02468
                               HOURS

    Figure 9.  Precipitation curves of  sediment measured  by cylinder.
           INITIAL   COAGULATED  FILTRATION  CHLORINATION
           LIQUID   SEDIMENT

Figure  10.  Reduction in  concentration of SS, COD and T-P  in each stage,
                                157

-------
   g

   15
   LJ
   O
      ppm

      60
       40
       20
                                 T-N
             INITIAL COAGULATED FILTRATION CHLORINATION
             LIQUID SEDIMENTATION
      Figure 11.  SS and T-N concentration at each stage.
.0
150    200   250    300     350 ppm
        500
                      2500 ppm
                      1000     1500     2000

                    ADDED AMOUNT OF  NoOCI

Figure 12.  Relationship between NH4 concentration  and amount of NaOCl.
                           158

-------
   Kg/cm2

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    0.4
E  0.2
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 O.I


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ง5 0.06
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   0.01
                                2.0-2.5m
                                   .0-l.8m
                                  0-0.5m
       0
                                       8
                      246

                          TIME  (DAY)

Figure 13.   Compression  strength  of sludge  after solidification.


          Kg/cm2



       x  '-ฐ

       fe 0.8


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 8
    O.I
     -EXPERIMENT ON SITE

      16.5% MIXED
                                            LABORATORY TEST

                                            15% MIXED
            L  'I     I    I    I     I    I    I    I     I
       0
                                      8
                      246


                              TIME  (DAY)

  Figure 14.  Comparison between  laboratory and on-site tests.
10
                     159

-------
              THE CONTRIBUTION OF SEDIMENT TO LAKE EUTROPHICATION
                         AS DETERMINED BY ALGAL ASSAY
                             Ryuichi  Sudo,  Chief
                         Mitsumasa  Okada,  Researcher
                      Freshwater  Environment  Laboratory
           The National  Institute  for Environmental  Studies, Japan
                                   ABSTRACT

     The  contribution of  sediment to  lake  eutrophication was  determined  by
using the blue-green alga Microcysti s aeruginosa, which is common in eutrophic
lakes and  reservoirs in  Japan.   Chelating  agents  in Gorham's  medium proved
necessary  for the  growth  of  M.  aerugi nosa and  it  was   determined  that  the
organics in the sediments, especially fulvic acid, played the same role as the
chelating agents in the growth medium.

     A large release of phosphate from sediments taken from Akanoi-wan in Lake
Biwa was observed during both aerobic and anaerobic incubation.   The growth of
M. aeruginosa  was  highly  stimulated by this material  released  from the sedi-
ment.   Under   aerobic  conditions,  some materials  that had  chelating effects
were  released from  the surface  layer  (0-9 cm)  of  sediments  at Akanoi-wan.
                                 INTRODUCTION

     The  bioassay  developed to  determine  nutrients  limiting  algal  growth in
lakes and rivers is called the "Algal Assay Procedure," abbreviated AAP (NERP,
1971).   It is used to assess the effect of wastewater discharge on eutrophica-
tion.   The  recent  increase in  eutrophication  in  Japan  has caused  many  re-
searchers and  adminstrators in  the  water pollution  control field  to become
interested in  AAP,  and many reports  on  the  application of  AAP  have begun to
appear  (Sudo et  al_. ,  1975;  Okada and  Sudo,  1978;  JSWG, 1976).   In almost all
the previous freshwater  studies  that used AAP, the  authors  selected Selenas-
trum capricornutum as  the  test alga.  Because this  alga  has never been domi-
nant in Japanese lakes there was a controversy over the appropriateness of its
use.

     Another standard  test  alga  in  AAP is M.  aeruginosa.   This  alga grows in
typical Japanese eutrophic  lakes  such as Kasumigaura  and  Suwako.   The forma-
tion of dense  blooms by  this  alga causes  many problems  including noxious
odors,  water treatment difficulties,  and fishkills.  Thus it appears desirable
to  use  M. aeruginosa  as  a test alga  in  AAP  not only  because  it is common in
Japan,   but  also  because the reason  behind  the massive blooms is  unknown  and
basic information is needed to predict their growth.


                                     161

-------
     The purpose  of this study was to  assess  the effect of  lake  sediment on
the growth of M.  aeruginosa.   This was done by  using AAP to:

     1)   study the  effects  of organics  in  the  sediment on the growth  of M.
          aeruginosa,

     2)   study the  effects  of  materials released  from the  sediments  under
          both aerobic and anaerobic  conditions  on the  growth of  M.  aerugin-
          osa.
                             METHODS AND MATERIALS
CULTIVATION OF ALGAE
     The alga used  in  this  study was Microcystis aeruginosa.   The test strain
was obtained  from the  National  Environmental  Research  Center,  U.S.  Environ-
mental  Protection Agency,  Corvallis,  Oregon.   Gorham's medium was used for the
stock culture medium  (Table  1)  (Okado and Sudo,  1978).   Stationary test tube
culture was satisfactory for maintaining the stock culture.
TABLE 1. COMPOSITION OF GORHAM'S NO.
11 MEDIUM

Material
NaN03
MgS04 • 7H20
CaCl4 • 2H20
K2HP04
Na2C03
Fe Citrate
Citrate
Na2EDTA
Na2Si03 • 9H20
* Gaffron's trace elements
Disti 1 led water
Amount
496.0 mg
75.0 mg
36.0 mg
1 .4 mg
20.0 mg
6.0 mg
6. 0 mg
1.0 mg
58.0 mg
0.8 ml
999.2 ml
                            Gaffron's trace elements
H2B04
MnS04 • 4H20
ZnS04 • 7H20
(NH4)6Mo7024 • 4H20
CO(N03)2 • 4H20
Na2W04 • 2H20
KBr
KI
Cd(N032) • 4H20
NiS04(NH4)2S04 • 6H20
VOS04 • 2H20
A12(S04)3K2S04 • 24H20
1/10 N H2S04
3100
2230
287
88
146
33
119
83
154
198
20
47
1000
mg
mg
mg
mg
mg
mg
mg
mg
mg
mg
mg
mg
ml
                                     162

-------
     Precultivation of the inoculum was conducted following the same method as
the algal assay.   In  this case, Gorham's medium was diluted to 1/5 concentra-
tion and provided  as  a preculture medium.  This  is because the high nutrient
concentration  in  full-strength Gorham's  medium may produce  an  inoculum that
contains excess nutrient  pools within the cells which would result in a maxi-
mum cell concentration and produce serious errors.

     This algal assay  medium was  also tried as a stock and preculture medium,
but the  results were  not satisfactory.  The water  samples  were  sterilized by
filtration  through  a  Millipore (0.45 u)  filter  to prevent  contamination by
indigenous  algae.   Erlenmeyer  flasks  (500 ml) were used  for culturing.   The
flasks were  cleaned carefully and 100 ml quantities of water samples or media
were  added.   A 7- to  10-day-old  culture of M. aeruginosa  in the exponential
growth phase was  washed  twice and inoculated  into  the medium or water sample
to give  an  initial  concentration  of 10,000 cells/ml.  The inoculum concentra-
tion was set lower than  called for  by the AAP to prevent nutrient carry-over
with the inoculum cells.

     Cultivation  was  conducted  in  a  constant  temperature  room  (25  ฑ  1ฐC)
equipped with  "cool  white"  fluorescent  lighting providing  a constant light
intensity of 500  lux.   The  flasks were  set on a rotary shaker  and shaken at
100  osci1lations/min.   Algal  biomass was  monitored using a  Coulter Counter
Model ZF equipped  with  a mean cell volume computer.  From the cell counts and
mean  cell  volume  of the  test  alga,  the total   cell  volume  was calculated and
this  volume converted to  dry weight  (mg/1).   Biomass  measurements were con-
tinued at 2-  to  3-day intervals  until  the  biomass  of alga reached a maximum.

HUMIC AND FULVIC ACID  EXTRACTION FROM  LAKE SEDIMENTS

     Humic  acid  and  fulvic  acid were  extracted  from  the  Kasumigaura  Lake
sediments sampled  with an Ekman dredge.  A 100 g (wet weight) sediment sample
was mixed with  300 ml  of 0.1N NaOH and shaken 24 hrs (Figure 1).  The extract
was  separated  by   filtration  and  adjusted  to  pH 3  using 0.1N HC1.   After 24
hours the  humic  acid  had  precipitated and the fulvic  acid  still  remained in
the supernatant.   The  precipitated humic acid was washed twice with distilled
water and   then  dissolved with 0.1N  NaOH.   The  concentration  of  humic  and
fulvic acid were measured using Chemical Oxygen Demand.

STIMULATION OF GROWTH  BY HUMIC AND FULVIC ACIDS

     Gorham's medium was used as the basic medium to which was added humic and
fulvic  acid to assess their  effects  on algal  growth.   It  is  well  known that
these acids are  natural  chelating  agents,  so the effects  of  the chelating
agents  already contained  in  Gorham's medium  were determined  prior  to  the
experiment.

ALGAL ASSAY ON SEDIMENT EXTRACTIONS

     To   assess  the influence  of  sediment on algal  growth,  core samples were
taken from  the sediments  at Akanoi-wan and Kusatsa Yamada-oki  in Lake Biwa.
The samples  were  frozen  at -70ฐC  as soon as possible after sampling, and then
freeze-dried.  The  freeze-dried  samples  were  mixed with  lake water from the
sample  site which  had  been passed  through  a  1.2 |j  Millipore  filter.   The


                                     163

-------
    SUP.
             SAMPLE
                    •O.I  N-NaOH
            FILTRATION
            FILTRATE
       SOLID
                   •1.0 N-HCI,  pH = 3
              12-24 MRS
           CENTRIFUGE
PT.
  FULVIC ACID
                              DISTILLED WATER
                       CENTRIFUGE
                           PT.             SUP
                              •O.I N-NaOH, pH= 13
                      HUMIC ACID
Figure 1.  The procedure for extraction of humic and fulvic
         acid from sediment samples.
                       164

-------
mixture was  1  g  sediment/liter.   This was transferred to a 1-liter Erlenmeyer
flask  and  magnetically stirred  and  incubated in  a  constant  temperature room
held at  20 ฑ  1ฐC.  An  aerobic  condition was maintained  by aeration  from the
bottom of  the flask  with  ammonia-free  humidified air which  had been passed
through saturated  boric  acid and distilled water.   For  maintaining an anaer-
obic condition,  the  dissolved oxygen in the lake water was purged by nitrogen
gas  before mixing  with the sediment  and  sealed tightly  during incubation.
Dissolved oxygen levels were maintained below 0.5 mg/1.

     Ammonium  (NH4-N),  nitrite  plus  nitrate (N02  +  N03-N)  nitrogen and phos-
phate  (P04-P)  concentration released from the sediment  were  monitored during
incubation.   DO,  pH,  and  redox  potential  were also  measured  to determine if
conditions were aerobic or anaerobic.

     The  algal  assay of the sediment was conducted  after  2  weeks of incuba-
tion.  Any  suspended  solids in the mixture were separated by centrifuging and
the  supernatant  was  axenically  filtered through  a  sterile 0.45  p Millipore
filter.  Disodium  ethylenediamine  tetra-acetate  (Na2EDTA) at 1 mg/1, P04-P at
0.1  mg-P/1 ,  and  N03-N at 2.0 mg-N/1  were  added  to the medium to estimate the
nutrients  limiting  algal  growth  and the effect of FDTA on M.  aeruginosa.  All
lake water was filtered prior to the algal assays.


                             RESULTS AND DISCUSSION

EFFECT OF CHELATING AGENTS ON THE GROWN OF M. aeruginosa

     The effects  of  chelating agents in the Gorham's medium  on M. aeruginosa
were studied  prior to adding humic and fulvic acids  (Table 2).  Ferric chlor-
ide  or ferric  citrate was the iron  source  at  concentrations  of 0.007, 0.014,
and  0.028  mg-Fe/ml ,  and Na2EDTA (0.3 mg/1)  or  citric acid (0.5 mg/1) was the
chelating  agent.   These  amounts  were  added  to   the  basic medium  (Table 1)
without Na2EDTA, citric acid, and ferric citrate.   The values shown in Table  2
are  maximum cell  concentrations  (mg/1)  for  each  combination.   The highest
concentration  was  observed  with  the combination of ferric citrate and Na2EDTA
+  citric  acid.   In the cases where ferric citrate was not used, M. aeruginosa
grew with  only the addition of  Na2EDTA  and  citric acid, but the maximum con-
centration was  lower  than  with ferric  citrate.   It  was  concluded, therefore,
that  an   iron  source  such  as ferric  citrate  and a chelating  agent  such as
Na2EDTA were necessary for the growth of M. aerugi nosa.


TABLE 2.   EFFECTS OF  IRON AND CHELATING AGENTS ON THE GROWTH OF M. aeruginosa
          [Values are maximum growth (mg/1)]
               cone.

Chelating Agents Cone":
                                FeCl
                              Fe citrate (mg/1)
0.007
0.014
0.028
0.007
0.014
0.028


Citri
Citri

d;
C
C
CRT A
> hU 1 A
Acid
Acid

.
0.
+

mg/ I
5 mg/1
Na2EDTA

.
0.
70.
1
1
0

H"7 O
/ . y
0.0 0.0
38. 21.


0.
180


0



0.0
160


0.0
150
                                      165

-------
EFFECTS OF HUMIC AND FULVIC ACIDS ON THE GROWTH OF M.  aeruginosa

     Humic and  fulvic  acids  are natural chelating agents which  may stimulate
the growth of  M.  aeruginosa.   Figure 2 shows the growth curve for M.  aerugin-
osa when grown in the basic medium (including chelating agents).   The addition
of  each acid  increased the  maximum  specific  growth  rate  from  0.25/day  to
0.4/day,  In the  instance  where 12.5 mg/1  fulvic acid was added, maximum cell
concentration  increased as well.   The lag  phase was  prolonged when humic acid
was added and  the  maximum  cell  concentration was not much different from that
grown on the basic medium.

     Figure 3 shows the results  of a similar experiment except that no chelat-
ing agent  was  used  in the basic  medium.   In all cases, the  specific growth
rate of M.  aeruginosa  was  decreased, and without either humic or fulvic acids
the growth rate  of the control  was only O.I/day.   With the  addition of fulvic
acid at  12.5 mg/1, the growth  rate  doubled to 0.22/day  and  the maximum cell
concentration  at 34  mg/1 was  three times that of basic medium (11 mg/1).  The
humic acid sample  (7.3 mg/1)  also showed a  higher maximum  cell  concentration
of 17 mg/1.

     These results  show that both  fulvic  and humic  acid could  stimulate the
growth of M. aeruginosa.   Fulvic acid had  the most effect.   These effects are
not as  pronounced  as  those produced by  the  chelating agents  used in Gorham's
medium.

THE EFFECTS  OF WATER-EXTRACTIONS  OF SEDIMENT ON THE GROWTH  OF  M.  aeruginosa

     Core samples  taken at Akanoi-wan were separated into four  subsamples  by
depth:   0-4  cm, 4-9 cm, 9-14 cm,  14-24 cm.  Each sample was  incubated under
both aerobic and  anaerobic conditions and  monitored  for the  release of nitro-
gen and phosphorus.

     The concentration  of  P04-P released from the 4  different subsample types
during  a  55-day incubation period  is  shown  in Figures 4 and 5.   Under both
aerobic and  anaerobic  conditions,  the P04-P concentration in  the upper layer
was higher  than that  of the  lower layer.   The P04-P  concentration reached a
maximum of 0.8 mg  P/l  for  the aerobic experiment and 1.7 mg  P/l  for anaerobic
conditions over 25 days.  A pH of 8.0 and redox potential of  410 mV were main-
tained throughout the aerobic experiment.  Under anaerobic conditions, a lower
pH  of  6.8-7.5  was observed and the  redox  potential  decreased from 400 mV  to
100 mV  after a day and remained there  during the rest of the incubation per-
iod.

     The  effect  of different  incubating conditions on  P04-P  concentration  is
shown  in  Figures  6  and 7.   P04-P  concentrations under  anaerobic conditions
were higher  than  under aerobic conditions.  The  P04-P concentration  at the
time of sampling at the bottom and top of the water column was 0.14 mg P/l and
0.03 mg P/l  respectively,   therefore it is  likely that  the  sediments have a
high potential  for releasing phosphate under both aerobic and anaerobic condi-
tions.
                                     166

-------
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1.0



0.8
ฃ0.6

Q.
i 04
^j-
0
Q.
0.2


n
-
O Bottom - 4 cm
3 4cm- 9cm
C 9cm- 14cm
• I4cm-24cm
	
O
O ^
3
o
<•>
Q
w
08 C • •
0 1) A
Ll A •
m i i i i




O
3
Q
9


A 0

Sample : Bottom sediments of Akanoi-Wan
SS • IOOOmg/1
Room Temp: 20ฐ C
AEROBIC CONDITIONS
1 1 1 1 1 1 1
      0
           10
20         30         40
   TIME     (DAYS)
50   55
     Figure 4.  Concentration of PO.-P during aerobic  incubation of lake sediment from Akanoi-wan.
   1.8
   1.5
   1.2
en
E
   0.9
Q_
 I
(5
   06
   0.3
                O
r    O
   O
                            O
                                   O
                             Sample: Bottom sediments of Akanoi-Wan
                             SS     ; 1000 mg/1
                             Room Temp.: 20ฐ C
                             ANAEROBIC CONDITIONS
                 O  Bottom - 4 cm
                 •  I4cm-24cm
    0
      0
                                                                I
           10
20         30         40
  TIME    (DAYS)
                                                               j
50   55
     Figure 5.  Concentration of PO.-P during anaerobic  incubation of lake sediment from Akanoi-wan.

                                    168

-------
o
a.
    1.8 r-
    1.5
    1.2
   0.9
    0.6
    0.3
     0
                                       O
                               O
                                 O Anaerobic condition
                                 • Aerobic condition

                            Sample Bottom sediments of Akanoi-Wan
                                   10-4.0 cm)
                               SS; 1000 mg/l
                            Room Temp.:  20ฐ C
O
        D
                                                          I
                                                               I
       0
      10
20         30          40
   TIME     (DAYS)
50   55
Figure 6.  Concentration of PO.-P during aerobic and anaerobic incubation of lake sediment from
          Akanoi-wan  0-4 cm layer.
u.b


- 0.4
o>
ฃ
0.
'ซ• 0.2
0
Q.


0
r U
^ o
O
O


• •
0
O Anaerobic condition
• _ • Aerobic condition
V
Sample: Bottom sediments of Akanoi-Wan
(!4-24cm)
A * SS: 1000 mg/l
m Room Temp.: 20 ฐC
n I i i i ii

0 10 20 30 40 50 55
TIME: (DAYS)
Figure 7.   Concentration of PO^-P during aerobic and anaerobic incubation of lake sediment from
          Akanoi-wan  14-24 cm layer.

                                      169

-------
     Figures 8 and  9  show the release of NH4-N and N02  + N03-N from the sedi-
ments at  core  depths  of  0-4 cm  and  14-24 cm.  Under  anaerobic  conditions  a
high concentration of NH-N was released,  but N02 +  NO-N  was not detected until
after a  day of  incubation.   This means  that  denitrification  occurred  in  the
incubator which  suggests  that mainly  NH4-N would  be released  from  the sedi-
ments under anaerobic conditions.   But N02 and N03-N were found in the aerobic
incubator.  NH4-N was  detected only  at the beginning of the incubation period
and  then  decreased  due  to  nitrification.    Although  the  forms  of  nitrogen
released  were  different  under  aerobic  and  anaerobic  conditions,  the  amount
(1.2 mg  N/l)  of total  inorganic  nitrogen  (NH4 + N02 +  N03-N)  did  not change
except in the aerobic incubation  of the 14-24 cm core sample.   It  is generally
accepted  that  the  nitrogen  available for  the growth  of algae  is  inorganic
nitrogen, therefore the fact  that total  available  nitrogen was the same under
all  conditions  differs from the  case  of phosphate,  where the  type  of  ion is
significant.

     Another sampling  station at Kusatsu  Yamada-oki   is  not as  polluted as
Akanoi-wan.   Sediment from this station was separated into three subsamples by
depth in  the core:   0-2.5 cm, 2.5-7.5 cm,  7.5-12.5  cm.   The sediment in this
area was  grey  and  different  from the black sediment at  Akanoi-wan.   The P04-P
concentration  released  under  the  two  incubation conditions  from  sediments at
different depths is  shown in  Figures 10  and 11.  As at  Akanoi-wan, more P04-P
was  released  from  the  upper  layer,  but the  total  amount released  from  the
upper layer was one-half of that  at Akanoi-wan.  In the  7.5-12.5 cm layer,  the
P04-P concentration was lower than 0.1 mg P/l even  under anaerobic conditions.
It  is  possible  that this  is  because suspended  solids with  high  phosphorus
concentrations   have been  settling for  a  long time  at Akanoi-wan  but only
recently at Kusatsu Yamada-oki.

     Figures 12  and 13 show the  P04-P released from the 0-2.5 cm and 7.5-12.5
cm  layers  under different  incubation  conditions.    In  the  7.5-12.5  cm layer,
anaerobic  release  was  higher than  aerobic  release.   But, there  was  little
difference  between  aerobic and anaerobic  conditions in  the 0-2.5  cm layer.
This result  is  very different from that  at  Akanoi-wan.   Although the concen-
tration of  P04-P  released from the Kusatsu  Yamada-oki  sediment was very  low,
the  potential  for  sediment phosphorus released is high due  to the low P04-P
concentration  in  lake water;  i.e.  the  bottom had  0.21  mg P/l  and  the  lake
surface had 0.001 mg P/l as P04-P.

     Figures 14  and 15 show  the  amounts of  inorganic  nitrogen released  from
the  0-2.5 cm and 7.5-12.5 cm sediment layers.  Under both aerobic and anaero-
bic  conditions,  the release  of  NH4-N was  remarkable.   As  at Akanoi-wan,  the
maximum concentration  was higher  under anaerobic conditions; i.e. 0.76 mg N/l
for  the  0-2.5  cm layer and 0.5 mg N/l for the 7.5-12.5 cm layer.   In the  case
of  P04-P, there  was a large difference between Akanoi-wan and  Kusatsu Yamada-
oki;  however,  the  amount of  nitrogen  released  from  Kusatsu  Yamada-oki  was
roughly  half  that  of  Akanoi-wan.   The  results  under  aerobic conditions  show
that nitrification  did not occur in the  Kusatsu Yamada-oki sediment and  that
the  N02  +  N03-N  concentration was always  low.  This  is noticeably different
than the  case  at Akanoi-wan.   As at Akanoi-wan, the depth of sediment samples
made only a small difference.
                                      170

-------
1* 1.6
2
i \2
CM
0
z
ซ 0.8
o
05
^[>0.4
0
Figure 8.
^j HIIUCIVUIV; luiiumuii u .. ovmyic- ounvm acumicuia ui
• Aerobic condition NH<~N Akonoi-Won ( Bottom-4cm)
SS: 1000 mg/l
_ A Anaerobic condition N+02)N Room Temp.: 20ฐ C
A Aerobic condition NOs
A 0
A 2 ฐ
" •
AO ฐ •
ฃV A Al A Al A 1 1 1 ™
0 10 20 30 40 50 55
TIME (DAYS)
Concentration of NH.-N and NO,, + NCL-N during aerobic and anaerobic incubation of lake
sediments from Akan3i-wan 0-4 cm layer.
1.6
       1 2
       '•*-
| 0.8

05
        0
          0
               O Anaerobic condition
               • Aerobic condition     4
               A Anaerobic condition
               A Aerobic condition  NOs
                                 0
                     0
                                 Al
                                               Sample: Bottom sediments of Akanoi-Wan
                                                       (14- 24cm)
                                                  SS: 1000 mg/l
                                               Room Temp.: 20ฐ C
                                        1
               10
                                                         1
20         30         40
   TIME    (DAYS)
                                                                      0
                                                                    50   55
Figure 9.  Concentration  of NH.-N and NOo + NO,-N during aerobic and anaerobic incubation of lake
         sediment from  AkanoT-wan 14-24 cm layer.
                                      171

-------
   0.5



   0.4
 en
 E 0.3
Q_
 i  0.2
O
Q.
   O.I
    0
O Bottom - 2.5cm
• 7.5cm-12.5 cm
          O
            O
      0
    O
     10
                        O
20
       O
       Sample :  Bottom sediments of
               Kusatsu Yamada-Oki
          SS :  1000 mg /I
       Room Temp: 20ฐ C
       AEROBIC CONDITIONS
                                                    .
                                TIME
30
(DAYS)
40
                                                                       O
50   55
Figure 10.  Concentration of PO.-P during aerobic incubation of lake sediment from
          Kusatsu Yamada-oki.
u.o


- 0.4
E

Q_
Ij-0.2
O
Q.
0
(
Sample : Bottom sediments of Kusatsu Yamado- Oki
SS : 1000 mg/l
Room Temp. : 20ฐ C
- ANAEROBIC CONDITIONS
O Bottom - 2.5 cm
• 75cm- 12.5cm

O
O
O
D 10 20 30 40





O


I 1
50 55
                                TIME   (DAYS)
Figure 11.  Concentration of PO.-P during anaerobic incubation of lake sediment from
          Kusatsu Yamada-oki.
                                 172

-------
w.o
- 0.4
en
e
- 0.3

Q_
1 0.2
0
Q_
O.I

0
O Anaerobic condition
_ • Aerobic condition


—
O

2
o
_ Sample: Bottom sediments of
^ * Kusatsu Yamada- Oki
0* O SS: 1000 mg/l
0 Room Temp. : 20ฐ C
ปoO I i i i
0 10 20 30 40
TIME (DAYS)




O





(0-2. 5 cm)

1 )
50 55

Figure 12.  Concentration of PO.-P during aerobic and anaerobic incubation of lake sediment
          from Kusatsu Yamada-oki 0-2.5 cm layer.
  0.10
Q_
 .  0.05

o
Q_
            Sample : Bottom sediments of Kusatsu Yamada-Oki
                    (7.5 -12.5cm)
               SS  : 1000 mg/l
            Room Temp..  20 ฐC
                              0
                                      o
                         O
     0
                                              I
                                                 O Anaerobic condition
                                                 • Aerobic condition
              i
0
                    10
                                 20
                                  TIME
30
(DAYS)
40
50   55
Figure 13.  Concentration of PO.-P during aerobic and anaerobic incubation of lake sediment
          from Kusatsu Yamada-oki 2.5-7.5 cm layer.

                                     173

-------
     1.0
 I
 CJ
 O


 +  0.5

 c?
 05
  ro
 X
      0
             O Anaerobic condition
             • Aerobic condition
   NH4~N
             A Anaerobic condition  N02>

                                  N03
             A Aerobic condition
                                      O
                               O
                  O
              o
                 Sample: Bottom sediments of Kusatsu
                         Yamada-Oki (Bottom-2.5cm)
                     SS: 1000 mg/l
                 Room Temp.: 20ฐ C
                                                                           O
                                             1
                                                                     I
       0
                   10
20
                                   TIME
30

  (DAYS)
                         40
50   55
Figure 14.  Concentration of NH.-N and NCL + NO,-N
          lake sediment from  Kusatsu Yamada-Oki
                                            during aerobic and anaerobic incubation of
                                            0-2.5 cm layer.
LUr o
_ •
^ A
o> A
i
00
ง 0.5 -
+.
ro
O _
Anaerobic condition
Aerobic condition NH4~N
Anaerobic condition NOa .
Aerobic condition N03


O

O
Sample. Bottom sediments of Kusatsu
Yamada-Oki ( 7.5 - 12 .5 cm)
SS: 1000 mg/l
Room Temp. : 20ฐ C



O

05 •Q * •
- n <* 8
z O
n^
A
k A^\ A Al ^

1 1 \ KL
       0
                   10
20         30         40
   TIME     (DAYS)
                                    50    55
Figure 15.  Concentration of NH.-N and N0? + NO,-N during aerobic and anaerobic incubation of
          lake sediment from Kusatsu Yamada-oki 7.5-12.5  cm layer.

                                      174

-------
     A  14-day-old  sediment-lakewater extract was  used for  the  algal  assays.
Because  the  P04-P  concentration  was  very  high,  a  dilution technique  was
adopted to  assess  the  algal  growth potential (AGP)  of  the sample water.   AGP
was calculated using the following equation:

       AGP (mg/l)= maximum cell concentration (mg/1) x dilution ratio.

     The nutrient concentration  and  AGP of samples  from  Akanoi-wan  are  shown
in Table 3  and  Figure  16.   AGP  in  lake water increased from 6.9 mg/1  to 15.2
mg/1  by  introduction of  EDTA.   A nutrient pulse test showed higher AGP values
than in the  case  of the nitrogen pulse test,  but it is difficult to conclude
that nitrogen was the limiting nutrient.


TABLE 3.  NUTRIENT CONCENTRATIONS IN AKANOI-WAN WATER SAMPLES USED FOR ALGAL
          ASSAY
                         Total P
P04-P
NH4-N
N02+N03-N
Filtered lake water
0.0-0.4 cm
0.0-4.0 cm
4.0-9.0 cm
9.0-14.0 cm
14.0-24.0 cm
14.0-24.0 cm
Oxic
Anoxic
Oxic
Oxic
Oxic
Anoxic
0.029
0.510
2.30
0.496
0.394
0.261
0.738
0.027
0.440
1.83
0.304
0.304
0.190
0.452
0.034
0.08
0.09
0.05
0.08
0.06
0.05
0.025
1.06
0.00
0.89
0.88
0.90
0.00

     The AGP was high in the anaerobic water extract from the upper layer (0-4
cm, 4-9  cm).   This seems to  be  caused by the high  concentration  of nitrogen
and phosphate released from the sediment.   However, the AGP of the lower layer
(9-14 cm,  14-24  cm)  was very low even though the nutrient concentrations were
high.   By  adding EDTA,  the AGP of  the  lower layer  increased to  the  level  ot
the upper layer without increasing the AGP of the upper layer.   It is possible
that materials  similar  to  EDTA released nutrients in the upper layer, but did
not release them from the lower layer or did release some kind of algal  growth
inhibiting materials.   A nutrient pulse test showed that  the  amount of phos-
phate released was much greater  than expected based on the N/P ratio required
for the growth of M.  aeruginosa.

     An  aerobic  sediment extract  showed  very low  AGP in both  the  upper and
lower layers.   This result seems  to be caused by a low nitrogen concentration.
The  same results  were  obtained  from  the  nutrient pulse  test,  i.e.  AGP  in
nitrogen spiked samples  was very  high.

     The nutrient  concentration  in water samples  from  Kusatsu  Yamada-oki are
shown  in  Table 4  and  the AGP  is shown  in  Figure  17.   The AGP  of  sediment
extract  with  a pulse of  EDTA added  was  higher than  that without  EDTA.   The
growth stimulation  effect  that was  observed in the  sediment  from Akanoi-wan
did not  appear.   Although the concentration  of  P04-P was lower  than that  of
Akanoi-wan, the P04-P released from Kusatsu Yamada-oki  caused a high AGP value
where a nitrogen pulse was  added.

                                      175

-------
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                                                                   i
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                               176

-------
   100
CP
E
LJ
X
I-

o
cr
o
    50
     0
                              TEST ALGA
                                       S
                                       E
                   M. oeruginoso
                   Standard
                   EDTA(1mg/l) added
                N:  N03-N(2mg-N/l)added
                P:  P04-P(0.lmg-P/l)added
         SAMPLE: Bottom sediments of
                  Kusatsu Yamoda-Oki
            FILTERED
AEROBIC
ANAEROBIC   ANAEROBIC
                        BOTTOM -  2.5cm
                                             I
                      7.5-I2.5cm LAYER
      Figure 17.   Algal growth potential (AGP) of lake water and
                 sediment extracts  from Kusatsu Yanada-oki.
                              177

-------
TABLE 4.   NUTRIENT CONCENTRATIONS IN KUSATSU YAMADO-OKI  WATER SAMPLES USED FOR
          ALGAL ASSAY


                         Total  P        P04-P        NH4-N        N02+N03-N
Fi
0.
0.
7.
Itered lake water
0-2
0-2
5-1
. 5 cm
. b cm
2.5 cm
Ox ic
Anoxic
Anoxic
0
0
0
0
001
132
199
032
0
0
0
0
000
122
159
018
0.
0.
0.
0.
07
28
12
08
0
0
0
0
01
04
00
01

           THE EFFECTS OF SEDIMENTS ON THE GROWTH OF M.  aeruginosa

     Chelating agents such  as  EDTA and ferric citrate  play  an  important role
in the growth of M.  aeruginosa.   The origin of these chelates in natural  water
is in the  sediment  or metabolites from algae, bacteria,  and other organisms.
In this research, fulvic  acid  extracted during the  spring  from lake sediment
showed a growth stimulation effect; a more remarkable effect was observed when
fulvic  acid  was extracted  from  highly polluted sediments  in  summer.   Tnere-
fore, it  can be concluded  that  the  sediments  play an important  role  in the
growth of M.  aerugi nosa.

     Algal assays were conducted  on sediments sampled in  Lake Biwa to clarify
the  differences  between  sampling  stations  and sediment  depth.   Higher AGP
values were  observed  in  the polluted Akanoi-wan sediment  extracts compared to
the  less   polluted  Kusatsu  Yamada-oki  sediment  extracts.   This  difference
resulted not  only from  the  large amount of  nutrients  released  from the sedi-
ment  at Akanoi-wan,  but also  from  the  release  of materials  equivalent to
chelates.   Since  these  chelating  agents  were  not  released under anaerobic
conditions,  the polluted  sediment appears  to stimulate the growth of M.  aeru-
ginosa even under aerobic conditions.

     Advanced  wastewater  treatment  and  nutrient  capture  or   diversion  are
regarded as effective methods for lake reclamation.  However, not all of these
techniques result  in  success  because  of  internal  phosphorus  loads  (Welch,
1977).   It  is  therefore important  to  prevent the  release of  nutrients and
organic materials  not  only to  reduce  internal  nutrient  loads, but  also to
decrease the  concentration of materials which stimulate algal growth, particu-
larly for the troublesome blue-green algae, M. aeruginosa.


                                  REFERENCES

Hughes,  E. 0., P.  R.  Gorham and U. A.  Zehnder (1958).  "Toxicity of a Unialgal
     Culture   of Microcystis  aerugi nosa."   Can.  J.  Microbiol., 4, pp. 225-236.

Japan Sewage Works  Cooperation (1976).   "The Development  and Applications of
     Indexes  for the Control of Eutropication" (in Japanese).

National Eutrophication Research  Program, U.S. Environmental Protection Agency
     (1971).   "Algal Assay Procedure Bottle Test."


                                      178

-------
Okada, M. , 0.  Yagi  and R. Sudo (1978).  "The Growth Stimulative Materials for
     Microcystis  aeruginosa."   43rd Conf.  of Japan  Society  on Limnology, pp.
     129.

Okada, M.  and  R. Sudo  (1978).   "Some Problems in Algal  Assay Procedure" (in
     Japanese).  Water and Wastes, 12, pp.  765-779.

Sudo,  R. ,  T.   Mori,  H.  Ohtake, M.  Okada,  and S.  Aiba  (1975).   "Algal Growth
     Potential  of Secondary  Effluents from Municipal Sewage Treatment Plants"
     (in  Japanese).   J.  Japan Sewage Works  Association,   12,  (6),  pp.  1-9
     (English  Translation).   In:   Research Treatises on Environmental Protec-
     tion  Technology  in  Japan, Research Coordination  Division, Environmental
     Agency,  Japan,   pp.  1-31.  (1977).

Welch, E.  B.  (1977).   "Nutrient Diversion:  Resulting  Lake  Trophic State and
     Phosphorus  Dynamics."   U.S.  Environmental  Protection  Agency, Corvallis,
     Oregon,  EPA-600/3-77-003.
                                     179

-------
           TOXIC MATERIAL AND NUTRIENTS FROM CONTAMINATED SEDIMENTS
                     Yoshiharu Nakazono and Yasuji Saotome
                              Machinery Division
                      Port and Harbor Research Institute
                         Ministry of Transport, Japan
                                   ABSTRACT

     This paper describes  the  characteristics of PCB (polychlorinated biphen-
yls),  mercury,  phosphate-P,  and  nitrogen  from  contaminated  sediments.   It
discusses the adherence of these materials to soil particles, their removal by
coagulants and a sand filter, and their solubility in water.

     The smaller the soil particle size, the higher the content of PCB or mer-
cury.  Phosphate-P  can  be  removed by the addition  of  certain coagulants, but
mercury, PCB, and nitrogen cannot be removed by the coagulating agents used in
this work.  PCB and mercury are readily removed by suspended solids.


                                 INTRODUCTION

     Contaminated  bottom  sediments,   for  reasons  of  pollution  control  and
environmental preservation,  must  be  removed as soon as  possible.   Removal is
currently done  by  using conventional  dredging and reclamation systems.   These
techniques require  great  care  to avoid secondary pollution  such as  dredging-
caused  turbidity  or wastewater  discharged  from  a  reclamation  site.   Various
dredges  and  reclamation methods  have  been  designed to  deal  with these prob-
lems.   Sediments  removed and  sent to  reclamation  sites must  be enclosed by
bulkheads, and wastewater discharged to the sea must meet standards set by the
Cabinet  Order  for  Implementation  of  the  Marine  Pollution Prevention  Law.
These  are  shown in  Table  1.  The removal  standards  for sediments containing
mercury  and  PCB  are established by the government.   In  accordance with these
criteria, sediments  containing  more  than  25 ppm mercury in rivers and marshes
are  subject  to removal,  and the  ocean criteria are  determined  by  the  mean
range, solubility  ratio  of mercury from the  sediments,  and  the safety factor
relative to any fisheries in the area.   Any bottom sediments with more than 10
ppm of PCB should be removed.

     Red  tides  will  result from  eutrophication caused  by the  discharge of
wastewater from  industrial  plants  or  by the  dumping  of domestic wastewater,
which provides nutrients such as nitrogen and phosphate-P.
                                      181

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                 TABLE 1.   EFFLUENT STANDARDS (June 21,  1971)
     Toxic Substances
Permissible Limits (mg/1)
     Cadmium and its compounds

     Cyanide compounds

     Organic phosphorus compounds
     (parathion, methyl parathion,
     methyl demeton and EPN only)

     Lead and its compounds

     Chromium (VI) compounds

     Arsenic and its compounds

     Total  mercury

     Alkyl  mercury compounds

     PCB
          0.1

          1

          1



          1

          0.5

          0.5

          0.005

     Not detectable1

          0.003
 1 "Not detectable"  means  that the substance is below the level  detectable by
the standard  method designated  by  the Director General  of  the  Environmental
Agency.
                         STUDY METHODS AND PROCEDURES
SEDIMENT SAMPLING
     The contaminated sediments  used  in this study were  sampled  at Tagonoura
Port for  PCB  and nitrogen, at Nagoya  Port  and  Tokyo Bay for mercury,  and at
the mouth of the Tama River for phosphate-P.   PCB at Tagonoura Port originated
in the wastewater from paper mills which used to produce paper containing PCB.
Straw chips and  coarse  rubble were removed  from  the  samples  according to the
standard method.  Samples  were  collected with Koken and Kumada-type samplers.
The former  is  a  grab sampler and the latter is  a dredge sampler.   The samples
were packed in  polyethylene  bags.  Their  identification and  conditions  are
shown in Table 2.

     In this study the following tests were performed:

                    1)   Sedimentation Test
                    2)   Filtration Test
                    3)   Solubility Test

     Concentrations  were  determined for  PCB,  total mercury,  phosphate-P and
total  nitrogen  according  to standard  methods.   It  is  not  necessary  to be
concerned about  detection  limits in soil samples  because of  the  high concen-
                                     182

-------
                   TABLE 2.   SAMPLES AND SAMPLING CONDITIONS

Sample Date Conditions of Sediments
PCB-1 Nov. 1976 black, hydrogen sulfide smell
PCB-2
PCB-3 " " " " "
Hg-1 Nov. 1977
Hg-2
P-l Oct. 1976
P-2 " black, sandy
P~3 " black, clayey
N Nov. 1977 black, hydrogen sulfide smell
Depth Remarks
(m)
9.0
12.0
15.0
2.1
2.0 mixture
3.0
4.9
25.0
6.5

trations, but in water the detection limits are as follows for the instruments
and the sample volumes used:

                    1)   PCB -- 0.0005 mg/1
                    2)   Total Mercury -- 0.0001 mg/1
                    3)   Phosphate-P -- 0.003 mg/1
                    4)   Total Nitrogen -- 0.5 mg/1

     In performing these  tests,  both natural Tokyo Bay and seawater and arti-
ficial seawater  made from  "Aquamarine"  were  employed.   The  natural  seawater
was used for the PCB and phosphate-P analyses, and the artificial seawater for
the total mercury and total nitrogen analyses.

SAMPLE PROPERTIES

     Samples were analyzed for true specific gravity, grain size distribution,
ignition loss, and  the  content per weight  of  dried  sediment  for the items of
interest.   The  results  shown  in  Table  3 and  Figure  1  demonstrate  that every
sample consists  primarily  of  particles below 74 urn and that the true specific
gravity  is  comparatively  low because  of  the high  ignition loss.   All  the
samples were prepared by centrifuging at 3,000 rpm for 20 minutes according to
the standard method, and testing the resultant precipitate.

     The  preliminary removal  standard  for sea  bottom  sediments  containing
mercury is calculated using the following equation:
                                      183

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TABLE 3.
SAMPLE PROPERTIES


Sample
PCB-1
PCB-2
PCB-3
Hg-1
Hg-2
P-l
P-2
P-3
Content
(ppm)
PCB 52.9
10.9
6.2
T-Hg1 43.3
11.3
P04-P 1.363
1.238
0.986
Ignition Loss True
21.8
23.8
19.. 1
22.0
13.4
9.3
4.6
8.3
Specific Gravity
2.432
2.413
2.490
2.289
2.438
2.594
2.659
2.648
                T-N
                       6640
26.7
2.234
^-Hg,  P04-P,   and  T-N  mean  total  mercury,  phosphate-P  and  total  nitrogen,
respectively.
          where:
                               C = 0.18 -  ^ 1
                                          J   b

                         H = the mean range
                         J = the solubility  rate,  and
                         S = the safety factor.

For example, at  Nagoya  Port H,  J, and  S  are 1.53 m, 0.0077, and  50,  respec-
tively,  so  C  =3.5 ppm.   Consequently,  sediments at locations Hg-1  and  Hg-2
should be  removed.

     It is  interesting  to understand  how  the  material  is  contained  in  the
bottom sediments.  An  attempt was made to  obtain the relationships  between the
contents per weight of  dried sediment and particle size.   Samples, except for
PCB,  were  wet-sieved into several groups to  prevent variation in the contents.
The results are shown  in Figures 2-4.   The curve at Station Hg-1 has a peak of
Hg concentration in the  105 urn to 250  (jm range.   In general,  the  contents of
both  PCB and mercury  increase with decreasing particle  size, but for nitrogen
the content appears to  increase with increasing particle  size.   It is usually
considered  that  the amount  adsorbed  per  weight  of solid increases  with  the
solid's specific  surface area,  which  usually depends  on  decreasing particle
volume.   The high ignition loss led us to  attempt to relate ignition losses to
particle sizes.  The  relationship between ignition  loss  and nitrogen content
is shown in Figure  5.   Figure 6  shows  ignition  loss vs mercury content.   The
total nitrogen concentration  varies  linearly with ignition loss,  but there is
no correlation with mercury.

     Sand   used  for the  filtration test meets the standards set by  the Japan
Waterworks Association.    The  sand contains  very little dust, clay or flat or
weak grains.  Table 4  shows the properties  of the sand  and Figure  7 shows the
                                      186

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-------
grain size  accumulation curve.   The  coefficient of permeability  of  the  sand
layer as  used  for  filtration is based on the constant-head permeation method.
This value may differ from the permeability under use conditions.
                    TABLE 4.   PROPERTIES OF FILTRATION SAND
     Ignition    Effective      True Specific  Porosity    Coefficient of
     Loss (%)  Grain Size (mm)     Gravity       (%)     Permeability (cm/s)
      0.545
0.405
2.610
41.6
0.154
                              PRINCIPAL ANALYSES
SEDIMENTATION ANALYSIS
     Samples were  sieved to  below 420 urn  under  wet  conditions.   Suspensions
were made oy mixing the samples with 50 liters of either Tokyo Bay seawater or
artificial  seawater,  as  mentioned previously.   The  suspensions,  at  a  pre-
determined concentration, were stirred at 40-60 rpm for 10 minutes in a settl-
ing  cylinder 291  mm  in  diameter and  900  mm in  height.   Settling  time  was
measured  from  the  moment stirring  stopped.   The central  part of  the water
column was sampled at fixed time intervals.

     Increased  settling  rates  caused  by coagulants  were examined  under  the
conditions  shown in  Table 5.   Time-dependent variations  in SS  vs  material
concentrations are given  in Figures 8-11.

             TABLE 5.  SPECIFICATIONS FOR SEDIMENTATION ANALYSIS

Sample

PCB-1 \
PCB-2/

SS
(ppm)
3,000
6,000

Coagulant and Its
Addition Concentrati
no additives
aluminum sulfate 1
ferrous sulfate 1

on

00
00
Sampling
Time (min)
0, 5, 10, 15
30, 60, 120,
300, 600
unslaked lime 1 ,000


Hg-i\
Hg-2/


N




50
400
3,000
50
400
400
400
cation polymer
anion polymer

no additives

no additives
no additives
PAC 100
cation polymer 1
1
1









0, 5, 10, 15
30, 60, 300
600, 1440
same as
above


Particle
Size

sieved
below
420 pm



same as
above
same as
above


                                     191

-------
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      30
TIME  (min)
                                                           60
 Figure 8.  Variation of PCB concentration with time (see Table 8 for symbol
          identification).
                                192

-------
  1.5
-  15
   1.0
 o
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 CO
 CO
 CO
  0.5
    0
             i ซNi  11  "  i    r~~i  rj    i    i  i T i    i   r
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 -   5
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                 ^
  SSo ORDINATE
* 50  SS/SSo
* 400 SS/SSo
3 3000 SS/SSo   J
• 50 T-Hg x ID'4
• 400 T-HgxIO"3-
o 3000 T-Hg xlO"2-
                  10           100
                      TIME  (min)
                                      1000
    Figure 9.  Variation of T-Hg  concentration and SS with time
              (Hg-1).
en
   0L  0
                                     SSo ORDINATE
                                     50  SS/SSo
                                     400 SS/SSo
                                    D 3000 SS/SSo
                                    • 50 T-Hg x IO"4
                                    • 400 T-HgxIO"4
                                     3000 T-Hgx IO'3
                 10           100
                      TIME (min)
                                     1000
    Figure 10.  Variation of T-Hg  concentration and SS with
               time (Hg-2).
                           193

-------
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          III.    I    II
                                    SSo ORDINATE
                                  A 50 SS/SSo
                                  A 400  SS/SSo
                                  o 400  SS/SSo Inorg.
                                    400  SS/SSo Org.
                                  • 50 T-N
                                  • 400 T-N
                                  o 400  T-N Inorg.
                                         T-N Org.
     L  0
                                100
                        TIME  (min)
                                         1000
  Figure 11.  Variation of T-N concentration and  SS with
             time  (N).
                           194

-------
Effluent standards  require  reclamation  if  the concentration  is  greater  than
0.003 mg/1  for  PCB  and 0.005 mg/1 for  total  mercury.   As in Figures 8-11  the
relationships  between  SS  vs material  concentration  are  plotted  in  Figures
12-16,  but the  solid  lines  in these figures  are  based on the assumption  that
the material  is part  of  the suspended  solids,  that  is,  the  lines represent
(SS) x  (material  concentration).   In  Figure 12 the  measured values  of  PCB
concentration  deviate  from  the  line,  but Murakami's  (1921)  measurements  show
good agreement with the line.  PCB has extraordinarily high chemical stability
and is  flammable  only  at  very high temperatures.   Generally  speaking,  PCB is
not soluble in water,  but the forced stirring makes it possible for PCB to di-
ssolve  to  concentrations  of 0.3  to 5  ppm.   Also, studies have  shown  that if
surface active  agents  coexist with  the PCB,  then  its  solubility  increases.
For example,  10  ppm of "Tween 80" in  water is responsible for producing 10-20
ppm solutions of KC-200, KC-300,  and KC-400 PCB (Isono and Fujiwara).  Surface
active  agents  are  thought  to be  mixed in natural water  in  large quantities.
Considering  this  possibility—that the water of  Tokyo Bay  contains  surface
active agents— the PCB  contained in  soil  particles may dissolve in sea water
from both  the  stirring and  surface active agents  and  then adhere to particu-
lates as they  settle,  consequently,  reducing the water column concentrations.

     To test  the  above assumption the  following  experiment was  conducted.   A
mixture of artificial  seawater,  surface active agent,  and PCB was  allowed to
settle and a sample of the upper water layer was taken after  a two-hour settl-
ing period.  The test conditions were:


SUBSTANCE                                                   QUANTITY

PCB (KC-400)	3 grams
Surface active agent [Dodecyle-benzol  sulfonate (DBS)]. . . 0, 0.03, 0.1,  0.3,
                                                            1.0, 10 mg/1
Seawater	3 liters
     The results of this experiment indicate that the surface active agent has
no apparent effect on the solubility of PCB in water (Table 6).


 TABLE 6.  PCB SOLUBILITY AS A FUNCTION OF SURFACE ACTIVE AGENT CONCENTRATION


     DBS Content (mg/1)       0      0.03    0.1     0.3     1.0     10.0

     PCB solubility (mg/1)  0.0153  0.0155  0.0159  0.0158  0.0143  0.0155
     The  solid line  in  Figure  13  indicates  good  correlation  between  T~Hg
concentration  and SS  when  the  latter  exceeds  50  mg/1.   It  shows  further,
however,  that the  correlation decreases  sharply  when SS  concentrations  are
less than 50 mg/1.  For the Hg-2 sample (Figure 14), which is a mixture of two
bottom sediments at Tokyo Bay and Nagoya Port,  the solid line corresponds well
with actual  measurements.   For P-l,  P-2, and P-3 (Figure 15), there exists no


                                     195

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relationship between  SS and  phosphate  concentration, but it  is  deduced from
the figure  that  coagulation  agents  such as aluminum sulfate,  ferrous sulfate,
and unslaked lime  have  the same effects as  removal  of soil  particles.   It is
found that  polymers  have  no  effect.   Phosphate-P dissolves in water from soil
particles in the  form  of  ions and exists in the suspension regardless of soil
particles, but the inorganic  coagulants and the ions unite and settle as solid
particles.  With regard to N  the relationship between total nitrogen and SS is
net  strong,  in  addition  none  of  the coagulants  appear to  remove  nitrogen.

     From the above  results,  it is  clear that it is possible  to monitor water
quality  by  means of  SS instead of  direct measurements  for  total  mercury or
PCB, i.e.,  water  quality  may meet effluent  standards  by keeping  SS less than
100 mg/1 for Hg-1 and less than 300  mg/1  for Hg-2.

     Sedimentation of  soil  particles  can  be  generally  classified  into three
types:   (1) discrete settling which  occurs when SS is very low; (2)  flocculant
settling, and (3)  zone  settling.   Consider a standard settling model based on
the  assumption  that  individual particles  behave  according  to  Stokes1  Law.
This model  fits  the  type  2 settling classification.  The following  discussion
shows  how  the  settling curve  takes the  shape  of  that  of  the  Hg-1  sample.

     Assuming that the  grain  size  accumulation  curve  takes  the shape  of  a
logarithmic normal distribution,  and denoting the particle diameter by x, the
curve can be described by the equation
F(x) =
exp[ -
                                                                           (1)
                         V27TO  -o

where  F(x) denotes  percent by   weight of  soil  particles  below x,   ฃ = Inx,
m  =  In VX84 X36>  a  =  In Vx84/xie-    For the  Hg-2 sample,   from Figure 1,
m = 2.965 and a = 0.999.

     According  to  Stokes'   law,  the  settling  velocity  of particles  having
diameter x is represented by the equation

                                       - p)z
                                  _ _ _
                                     18u

Let p(x)dx represent the percent weight of soil  particles having velocity v in
the suspension whose  initial  SS is equal to  SS0.  Let SS at a distance z from
the surface be SS, and elapsed time after stirring be t, the equation
           SS/SSo =
       p(x) dx
                                                                           (3)
is obtained.   Since dF(x) = p(x)dx, v = z/t, it becomes

                                   ln
SS/SS0 =
                    exp
                                               _  }
                                                 m}
                 ] d|
                                                                           (4)
                                     199

-------
where a =  Vl^M/g  (p  ~ Pf)-  The  curve  obtained from equation (4) is plotted
in Figure  10.   This ideal  settling curve is influenced by convection due to a
temperature differential between the  upper and lower part of the water column
and the diameter of the container.   It is obvious from Figure 10 that sedimen-
tation is  better  when  SS0  is high.  Where  SS0  was  3,000 mg/1 , SS was reduced
to  1/10  of  SS0 in 30  minutes.   By  comparison  the  50  and 400  mg/1  initial
suspensions  show  a  slower  sedimentation  time  than  that of  the  theoretical
model.

     Increasing the  sedimentation  rate  by using coagulants  was investigated
using a  suspension  of  400  mg/1 of  SS  made from sample  N  and  artificial  sea-
water.   PAC  and cation  polymer were added separately to the suspension in the
amounts shown in Table  5.   Figure 11 shows the test results.  Sedimentation is
enhanced  by  addition of an inorganic coagulant agent  and  even more  by the
organic coagulants.

     The  above  results  show that  PCB  and mercury  bond strongly  with  soil
particles.   Therefore,   to  remove  PCB  or  mercury from  seawater,  it is suffic-
ient to remove  the  suspended solids.   Some coagulants are effective in remov-
ing  phosphate-P from  the  suspension, but they are  not useful  for removing
nitrogen.

FILTRATION TEST

     For this test  samples were passed through  a  sand filter.   The apparatus
was a vertical cylinder 3.2 m high with a 0.291 m diameter.   The filter column
was packed with sand  having grain size characteristics  as  shown in Figure 7.

     The tests were run by  pouring the suspensions  into the cylinder and, with
the  valve  left  open at the bottom, periodically sampling  the  filtered water
and  analyzing  it  for mercury,  PCB,  and  SS.  During  the  experiment the water
was maintained  at  a constant level by continually  adding more of the suspen-
sion being tested.  For example, Hg-1  measurements  were made of the filtration
ratio (which  is defined by the flow rate of the filtered water) and the level
of total mercury in the sand layer at the end of the test.

     It  is obvious  that  the  majority  of SS can  be removed  by filtration,
therefore  PCB and  mercury  should not penetrate the sand layer.  But note that
sediments  deposited on  the sand layer also  act  as  a filter.  These sediments
were several  millimeters thick.

     Figure  17  shows variations  in filtration rate with time.   The filtration
rate decreases  sharply  after several  hours.  The influences of water pressure
over the  sand  surface  on the filtration  rate is also illustrated.  A pressure
difference of 1 m of depth slightly increases the  filtration rate.  Figure 17
also compares the  filtration characteristics of the suspensions prepared from
sea bottom sediments sieved blow 420 urn and 74 urn.   The filtration rate of the
suspension below  74 pm is  greater  than  that of the  suspension  below 420 pm.

     Total mercury  in  filtered water is  shown  in  Figure 18.  The test condi-
tions  under  which the  results  in  Figure  18 were obtained  were  the only ones
that yielded detectable quantities of total mercury.  In this test, concentra-
                                     200

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-------
tion decreased sharply with  time.   Even after only one hour the concentration
of  total  mercury  showed only  0.0012  mg/1,  which  easily  meets  the  effluent
standard of 0.005 mg/1.

     The total mercury concentration at different depths in the sand layer was
measured and the results  are presented in Figures 19 and 20.   In Figure 19 the
mercury  does  not  reach  the  bottom of  the  sand  layer;  in  Figure 20  larger
amounts of soil  particles are found at the lowest part of the layer.   But even
in this case,  total mercury is not detected in the filtered water.  This leads
to the conclusion that in the early filtration process almost all  the  voids of
the sand layer are clogged by soil particles.

     The significant conclusion from the above results is that, except for the
early stages  of  reclamation  work,  a bulkhead built  of  earth and sand instead
of expensive watertight structures may prevent PCB or mercury from re-entering
the environment,  i.e., filtration through a sand layer of proper grain size is
an effective method for removing PCB and mercury.

SOLUBILIZATION TEST

     The  test was  carried  out  according to  the  Methods  for  Investigating
Bottom Sediments authorized  by the Environmental Agency, except that  artific-
ial seawater  and  natural  seawater were employed  in  preparing  the mixtures of
bottom sediments  and water.   The  mixture was  continuously  stirred  for  four
hours, and  after  being allowed to settle a bit,  it was passed through filter
paper.  The filtered water was analyzed for contents.  Conditions for  the test
are shown in Table 7.
                    TABLE 7.   TEST CONDITIONS AND RESULTS
     Sample    Mixing Ratio (g/ml)    Concentration After Filtering (mg/1)

PCB-1



Hg-1


50/100
25/100
3/100
0.3/100
3/100
1.5/100
0.3/100
0.03/100
0.0006
ND
NO
ND
ND
ND
ND
ND

Mixing ratio is the ratio of soil dry weights (g) to the volume of the mixture
(ml).

ND means  "not  detectable,"  i.e., 0.0005 mg/1 or less for PCB, and 0.0001 mg/1
for total mercury.


     The Methods for Investigating Bottom Sediments defines the solubilization
ratio as:
                                     202

-------
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                                               203

-------
                         Sol utilization ratio =
where Wx  is  the  amount of toxic matter  (pg)  contained  in the bottom sediment
sample, and  W2  is  the amount of  toxic  matter  (p.g)  which is contained  in  a
volume  of filtered  water equivalent  to the  mixture  prepared  in  the  test.

     According to  this definition,  the solubil ization  ratio  is  calculated  to
be less than  7.7  x 10-3 for  Hg-1  and  5.57  x 10-5 for PCB-1.   The preliminary
criteria for sea bottom sediments were  calculated using  these  values.

                                  CONCLUSIONS

     The main conclusions to be drawn from this study are:

1)   The finer the  particles  of  the bottom sediments,  the  higher the concen-
     tration of PCB and total  mercury.   They adhere strongly to soil  particles
     and it  is  therefore  important to  remove fine suspended solids to improve
     wastewater quality at reclamation  sites.

2)   Because  a  sand layer  can  prevent suspended  solids  from penetrating,  a
     bulkhead filter built  with  earth  and sand is capable of  removing PCB and
     mercury.

3)   Phosphate-P is  removed by  addition  of  aluminum sulfate,  ferrous sulfate,
     and unslaked  lime.   Except  for the  nitrogen  in  soil  particles, nitrogen
     will  not be removed by any coagulation  agent.

4)   Total  mercury concentration  in the  sand  layer  is  extremely   high  but
     decreases abruptly with  depth,  leading to the conclusion that almost all
     suspended solids  remain  in a  thin  layer  in the  upper part  of the  sand
     layer.   The filtration rate decreases sharply with  time.

5)   A  surface  active  agent  did  not  dissolve  PCB  in water under  the  test
     conditions employed  here.   During  the  test PCB was observed to fall  in
     spherical particles after stirring stopped.


                                     NOTES

1.   In the  sedimentation  test,  the direction of filtration was  in the verti-
     cal  direction,  i.e.,  the sand layer was horizontal,  allowing  suspended
     solids to fall  on the surface.  This test method is  not  capable of exam-
     ining the permeation of suspensions  through  bulkheads built  up with earth
     and sand.  But  for secondary  treatment of wastewater  that  does not meet
     the effluent standards, filtering  contaminated suspensions through a sand
     layer is an effective method of improving water quality.

2.   Regarding the  solubility  of PCB in  water:  the  surface  active  agent has
     no effect, but  it is possible that the  deviation  between the solid line
     and  the measurements  in Figure  12 may  be  due to  oil,  because  PCB  is
     soluble in oil.  We intend to clarify this point.
                                     204

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       TABLE 8.   SYMBOLS (APPLICABLE TO FIGURE 8,  FIGURE 12,  FIGURE 15)
         coagulation
                      no
                    addition
                         aluminum
                         sulfate
ferrous
sulfate
 am on
polymer
cation
polymer
unslaked
  1 ime
                      o
                                     a
     6,000
3.
                    REFERENCES (all  in Japanese)

Muramaki,  K.  and Takeishi, K.   "On the Behavior of Heavy Metals, PCB,  and
so  on   in  Management of  Hedoro,"  Proceedings  of  Port  and  Harbor  Tech-
niques, Bureau of Ports and Harbors, Ministry of Transport, No.  78,  1977.

Isono,   N.  and  Fujiwara,   K.   "Pollution  caused  by  PCB I," Journal  of
Science, Iwanami Publications, Inc., Vol.  42, No.  5.

"Collections of Hydraulic Formulas," edited by The Japan Society of Civil
Engineers.
                                      205

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                 THE FILTERING EFFECT OF CONTAINMENT WALLS ON
                 SUPERNATANT FROM CONTAMINATED DREDGE MATERIAL
                                 Takeshi Monji
                      Port and Harbor Research Institute
                         Ministry of Transport,  Japan


                                   ABSTRACT

     In designing revetments for disposal sites, care must be taken to prevent
pollution of the nearby environment from permeation of contaminated substances
through the containment wall.   This paper describes the results of the follow-
ing experiments:

     1)   Heavy metal  adsorption on clay
     2)   Filtration effects of sand backfill
     3)   Testing of steel piling seals for permeability

     These  experiments  produced  useful  data to help  design  containment walls
for land reclaimed with dredged material.
                                 INTRODUCTION

     The large cities  of  Japan,  such as Tokyo, Osaka,  and Nagoya are located
in the  coastal area.   The rapid economic development of  the  1960s caused en-
vironmental pollution  to  become  an  important problem along the  coast,  espec-
ially on the bottoms of some harbors, rivers, lakes and  marshes.   Contaminated
substances with undesirable effects  on the surrounding environment accumulated
in these areas.   Sources  of these sediments are usually from  waste discharges
from  manufacturing  plants,  mines,   urban  sewage,  or agricultural  effluents.

     To cope with this pollution, the government imposed legal  restrictions on
effluent discharges and began  to dredge the polluted sediments.   This  policy
resulted in  gradual  improvment  of  the environment,  but  large  quantities  of
sediment and urban waste  are a continuing problem.   One of the most difficult
tasks is to  find  disposal sites for  this  sediment  and  waste.   In Japan there
is no space for land disposal.   Therefore, sediment and  waste  has usually been
managed  as reclaimed  land  in  a port  area.   After a  period  of  time,  these
reclaimed lands have been  used effectively for port facilities, urban redevel-
opment,  distribution stations,  and  other  uses.   However,  it is  becoming more
difficult  to find appropriate  disposal  sites.   Construction of revetments for
dredged material  has  become more  complex because  of the  technical  problems
associated with  building  on thick  deposits  of  soft soils and in  deep  water.
The most important  consideration in constructing a containment  wall  for this


                                      207

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purpose is  to  prevent  secondary  pollution due to permeation  of  contaminated
substances through the  wall.   To  construct an absolutely waterproof revetment
is not  impossible,  but it  is  expensive  and unnecessary.  The author  and his
colleagues have  begun  studies  to  determine a safe, economical  structure for
revetments.   This paper is an interim report of these studies,  particularly on
the filtering effects of these porous containment  walls.


                       CONTAINMENT WALL  CHARACTERISTICS

TECHNICAL  CONSTRUCTION PROBLEMS

     Containment  walls  for  land  reclamation  have  different  characteristics
than conventional wharves  and  revetments.   First, conditions at  the construc-
tion site  are difficult because of soft  ground and deep water.   Second, design
variables  such  as  quality  of  material   for  reclamation,  the height  of the
structure,  and  the  residual water  level  are more  severe.   Third, and  most
important,  is  to prevent contaminated  substances  from permeating  the wall.
Though we can cope  with the first two problems using conventional techniques,
the  third problem  has unknown factors  such as  sand  filtration  effects and
permeation rates of contaminated substances.

     In Japan two types of containment  walls have usually  been  constructed—
the gravity  type  (caisson,  cellular,  stone masonry, etc.)  and the sheet pile
type (double wall,  steel  pile,  etc.).  Figure 1  shows  typical  Japanese revet-
ments for  reclaimed land.   Methods of protection against permeation of contam-
inated substances are discussed for both types.

TECHNIQUES TO PREVENT PERMEATION OF CONTAMINATED SUBSTANCES

     Techniques   to  prevent  permeation   of  contaminated  substances  through
revetments  are  shown  in   Figure  2.   They may be  classified  into  5  groups:

     1)   Protection Sheet.   Many  kinds  are commercially  available  and are
          effective  for  prevention   of  pollution.   However,  more study  of
          durability and  sheet  arrangement is necessary to make  practical use
          of this technique.

     2)   Backfill.   This  is often  used  as a protection  method  but a precise
          determination of  the  relationship of thickness and  grain size dis-
          tribution to permeation  of pollutants still remains unsolved because
          the sand filter mechanism is not yet fully understood.

     3)   Sheet Pile.   Piles are  usually  driven  into  the  impermeable  layers.

     4)   Grout.   Sheet pile joints  are  sometimes  sealed  with  asphalt,  ure-
          thane, or mortar.

     5)   Direct Mixing.   Direct  mixing  of asphalt or  cement  mortar with the
          disposed material.  This causes soil stabilization.

     In  constructing  revetments   it  is  impractical  to  make  them perfectly
watertight.   To prevent as much pollution as possible is the objective.  Thus,


                                      208

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the  purpose  of the  experiments  described in this  paper is to determine the
filtering effect of  sand  backfill  and fill  on the permeation  of  contaminated
substances and,  finally,  to determine  the  proper design criteria for  revet-
ments.
     METHOD
                                       KIND OF  WASTE
                                            TOTAL
    PROTECTION SHEET
                          8
    SHEET  PILE
    GROUTING JOINTS
    (Gravity type)

             A -Waste from manufacture including
                toxic substances
             B- General waste
             C - Others
    WIDENING OF BACKFILL
3321
    WIDENING OF BACKFILL
    PROTECTION SHEET
                                     (1975)
    GROUTING JOINTS
    SHEET PILE TYPE
Mfrl
    FILL (Celluler
           bulkhead)
     15
    Figure 2.   Techniques to prevent permeation  of  contaminated  substances.
                  SAND BACKFILL AS  A  FILTER  FOR  HEAVY  METALS

     Clay mainly  consists  of  silica,  alumina and  water.   Some kinds of clay
include magnesium, iron,  alkaline-metal  and  alkaline-earth-metal.  Clay grains
are  negatively-charged  from  ion  exchange  in the  crystals of  clay  and from
imperfections on  the  surface  of clay  particles.   Though the electric charge
depends  on  a  combination  of  factors,  heavy  metal is  generally  adsorbed to
clay.  This  is why  bottom  sediments  in the coastal areas  and  rivers in Japan
include some heavy metals which are deleterious  to  health.

     In  dredging  these  contaminated  sediments  and disposing of  them  as re-
claimed  land,  the  most  important considerations  are elution  of toxic sub-
stances by dredging, disposal  of the  supernatant water of dredged  sediment and
the permeation of contaminated  substances through  the containment area revet-
ment.
     If clay is put  into  a  solution containing heavy metal and agitated, the
heavy  metal  is adsorbed  to  the  clay.   So  when  contaminated  sediments are
disposed of as  reclaimed  land,  heavy  metals  in
the  suspended  soils  and  these  suspended soils
backfill sand in the  revetment.
                      the  water will  be
                      will be  filtered
adsorbed to
out  by  the
                                     210

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     By knowing the  rate  of adsorption of heavy metal to clay and the filter-
ing capacity of sand backfill  for suspended  soil,  the  concentration of heavy
metal   in  the  effluent from contaminated substances can  be controlled  at  a
level  which will  satisfy the requirements.

     These considerations allow revetments to be designed safely and economic-
ally by  determining the  kind  and thickness  of backfill  sand.   The filtering
effect  depends  on  both  adsorption of  heavy metal  to  clay minerals  and the
filtering out of  suspended  soils.   The amount  of  heavy metal  adsorbed to the
clay  varies  with  the  kind  of  clay,  type  of  heavy metal,  concentration  of
seawater, and the  pH of the suspension.  The filtering effect of sand changes
with the particle size of the sand, particle  size of the clay, water pressure,
density of sand and other factors.

CHARACTERISTICS OF MARINE CLAY AND BACKFILL SAND IN JAPANESE PORTS

     Coastal  Japan  is  covered  with soft alluvial clays which come from rivers
and in  some  cases  derive from volcanic ash.   Clay minerals are the result of
chemical weathering  of rock and consist  mainly of kaolinite,  montmorillonite
and illite.

     Clay particles  are  negatively charged.   Cations such as heavy metal ions
are thereby  adsorbed  to  the surface  of  the clay  particles.   The  higher the
electric charge  or  the  smaller  the radius  of the  cations,  the stronger the
adsorptive adherence.   The   present  experiments do  not investigate in detail
the chemical  reaction  of clays.   At  this  time  general  information  is more
useful in designing containment walls.

     Soil samples,  including sea  bottom  clay or  sand  used  for backfill were
collected from the  various  locations shown  in Figure 3.  Using these samples,
several series of  experiments  were made on  heavy metal adsorption to clay and
on the  filtering  effect of  backfill sand.   The physical  and chemical charac-
teristics of the clay and sand are given in  Figures 4 and 5 and Table 1.  With
few exceptions all the clays used have similar physical properties.

     The sands  have a  similar  pattern of  grain  size distribution, somewhere
between  the  Takahagi  sand  and  the Toyoura  sand used  in  the author's labora-
tory.    Backfill  sand  samples  were  made  by mixing  these  two  sands  for the
experiments.


                        EXPERIMENTS ON CLAY ADSORPTION

FACTORS CONTROLLING THE ADSORPTION OF HEAVY METAL

     The purpose  of this  experiment was  to  determine  the rate of heavy metal
adsorption on to  clay.   Lead,  cadmium  and  mercury were the heavy metals used
in this  experiment  and  Kawasaki  clay  was used for  the suspension.   The main
factors  considered  in  the   experiments  were  the  concentration of  the heavy
metals  and  suspensions  in  solution.   Additional  factors  investigated were
agitation time, mesh size of filter, position  of  the agitating apparatus and
pH.
                                      211

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                                                -AOMORI
                                           I  3
                        FUSHIKITOYAMA

                        KOBE
                                       NAGOYA
 Figure 3.   Main ports  in Japan  (clay  and  backfill  sand from these ports were
            used in the experiment).


     The heavy  metal  solution was  prepared  by dissolving bichloride of mer-
cury, cadmium nitrate  and lead nitrate in  fresh water  and  ion-exchanged water.
Five liters of undiluted solution,  including  clay,  were agitated  in a cylinder
by rotary  action  for 30 minutes.   After filtering,  the concentration of heavy
metal,  turbidity,  pH and other factors were measured.

     Results of this experiment  are:
                               ,    Co  - C   nnr,
                               A =  —p	  x 100
                                      o

          A:  Adsorption percentage
         Co:  Concentration of solution with  heavy  metal
          C:  Concentration of solution after being adsorbed onto clay

     (1)  Adsorption of mercury  to  clay increases  in  proportion to the loga-
          rithm of  turbidity, i.e.   70% for 100 ppm of turbidity  and more than
          80%  for  500  ppm of turbidity.   Lead and cadmium show the same  ad-
          sorptive tendency as mercury (see Figure  6).
                                     212

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            TABLE 1.   CHARACTERISTICS OF  CLAYS IN  JAPAN

Clay Type
Characteristics
Spec!!ic (Gs)
gravity
;;sd <ซป
"ป?t1c w %
?idซc1ty<*ป --
Gravel %
Sand %
Silt %
Clay %
Classification
Total -mercury ppm
Cadmium ppm
Lead ppm
Sulfide mg/g
pH
O.R.P. 100 mV
Aomori
2.56
70.4
46.7
23.7
0.5
14.0
55.2
30.3
F
0.36
0.75
56.1
1.90
7.9
-3.10
Kawasaki
2.69
75.6
37.8
37.8
0
4.7
38.3
57.0
f
0.33
0.23
39.4
0.28
8.4
-1.40
Nagoya
2.68
64.5
30.9
33.6
5.1
17.1
34.3
43.5
F
0.23
0.32
41.2
0.22
7.9
1.60
Fushiki
Toyama
2.66
63.8
32.9
30.9
0.2
19.5
51.9
28.4
F
0.48
0.64
35.9
2.30
8.0
-3.40
Kobe
2.70
100.4
39.2
61.2
0.1
1.1
36.3
62.5
F
0.17
0.24
40.2
0.21
7.8
0.60
Moji
2.70
76.5
29.6
46.9
0.3
10.2
30.5
59.0
F
0.05
0.10
19.9
0.06
7.7
1.40

(2)  Adsorption of heavy metal  to  clay is low in acid solutions (pH >_ 6)
     and  high  in  alkaline  solution  (pH <  7).    This  tendency  is  more
     noticeable for cadmium  and lead (see Figure  7).

(3)  Adsorption of each metal  when  all  three metals are  mixed together is
     the same as that for individual metals.

(4)  Changing agitation time (0.5-60 minutes) has no influence on adsorp-
     tion.
                                 213

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            I   I I  I II III
                                                   0 Aamori
                                                   A FushikiToyama
                                                   a Kawasaki
                                                    Nagoya
                                                    Kobe
                                                    Moji
      0.001
       0.01            O.I
           GRAIN SIZE  (mm)

Figure 4.  Grain  size distribution of clay.
  100
  80
LJ
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tr
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a.
   60
  40
   20
    0
                                     Akito
                                  -• Nigota
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                              A — A Kawasaki
                                     Shimonoseki 1
                              a --- a     "       2
                              D-— -a     n       3  _
     0.005   O.I                       I.O
                     GRAIN SIZE  (mm)
           Figure 5a.  Grain size distribution  of backfill  sand.

-------
                   100
                   80
                 o
                 cc
         40


         20
                       TTTTJ
                                        i  r
                                         A Toyoura
                                         o Takahagi
                    0
                    0.05  O.I
                          1 1 LIJl
1   1  1
     Figure 5b.
                        (mm)   1.0         5.0
      Grain  size distribution  of  sand used for the  experiment.
         100
        ui
          80
        ui
        o
        cr
        ui
        a.
          60
        Q.
        QL
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          40
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               III!

                           o Pb- Low O.I   ppm
                           • Pb- High  1.0
                           ACd- Low 0.01   "
                           ACd- High 0.10   "
                           a Hg- Low 0.005 "
                           • Hg- High 0.050 "
               i  I  I i
            50      100                500    1000
                              TURBIDITY   (ppm)
                                                      I
                    I
                                                   3000
Figure  6.
Adsorption of heavy metal  onto clay.  Note:   Adsorption percentage
A is defined as
                               _ Co - C
                                        x  100
         A:  Adsorption  percentage
        Co:  Concentration  of solution with  heavy metal
         C:  Concentration  of solution after being adsorbed onto  clay

-------
      100
    UJ
       80
    UJ
    o
    E  60
    CL
    -z.
    O

    t
    o:
    o
    CO
    Q
    <  20
        0
                                   O Lead (Pb)-1.0 ppm
                                   A Cadmium (Cd)-O.IO ppm.
                                   D Mercury (Hg)~0.05 ppm

                                     (Suspension-. 500 ppm)
          0       2        4       6       8       10
                                       pH
           Figure 7.   Relationship between pH and adsorption.
                                                            12
       (ppm)
 Pb  Cd    Hg
 1.0
0.8
0.6
04
0.2
  rO.IO
  ^0.08
  -0.06
  hO.04
  -0.02
rO.05
-0.04
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-002
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            0
                                    i i  i I I ii|    i   ill rj ill
ฐ(Pb)SS
• Pb
A(Cd)SS
A Cd
a (Hg} SS
• Hg
                                                        1000
(ppm)
 SS
5000


4000


3000


2000


1000


0
             I              10            100
                             TIME  (min)
Figure 8.   Change of heavy metal  concentration and SS in sedimentation test.
                                216

-------
EXPERIMENTS ON ADSORPTION AND SEDIMENTATION OF HEAVY METAL IN SEAWATER

     The purpose of  this  experiment was to investigate heavy metal  adsorption
onto clay,  and sedimentation  of  heavy metal  in seawater.   The  authors  used
Kawasaki clay  in  suspension  plus  mercury, cadmium, and  lead as heavy metals.
The  seawater  was  from  Yokosuka  in Tokyo  Bay.   The  heavy metal  solution was
prepared by  the same  method as described above.   The experimental  apparatus
was  an  acrylic  cylinder (d = 190 mm,  h = TOO cm).   The prepared solution was
poured  into  the  cylinder to 90  cm in  depth and  allowed  to settle  after  1
minute of agitation.   The solution was sampled by siphon at 45 cm of depth and
analyzed.  The results of this experiment are

     (1)  Clay particles flocculate in seawater and are deposited more rapidly
          than in freshwater.

     (2)  The concentration  of mercury and lead in the  solution  decreases in
          relationship  to  the sedimentation  of  clay  particles  (SS),  but the
          concentration of cadmium  in  the solution is unaffected by the sedi-
          mentation of clay particles (see Figure 8).

     This may  be  because  substances in seawater which are less easily ionized
than cadmium are adsorbed onto the clay.

EXPERIMENTS ON ADSORPTION OF HEAVY METALS TO SANDS

     The purpose of  this  experiment was to investigate heavy metal  adsorption
onto clay which is mixed with sand.  Factors such as clay fractions,  grain size
of sand  and  immersion time were considered.   Takahagi sand,  Toyoura sand, and
Kawasaki clay  sieved  through  a  0.074  mm mesh  and  seawater were  used.   The
solution, including  heavy  metal  but excluding clay particles, was prepared by
the  method described  above.   Samples  contained  in  acrylic cylinders  (d = 290
mm,  h = 100 mm) were made by mixing small  amounts of clay with sand  in differ-
ent  ratios  ranging from 0.001% to 5%.   The solution, including different kinds
of heavy metal, was  poured into each container.   The samples were left in the
container for from 30 minutes to 3 hours and the filtrate was analyzed to find
the  adsorption of  heavy  metal  to clay.   Results  of these  experiments  are

     (1)  Adsorption  of  mercury  increases in proportion  to  the  clay  fraction
          regardless  of  immersion time  and  the percentage  of adsorption was
          the same as that in the suspension.

     (2)  Adsorption  of  cadmium  is  30%-50% regardless of  both immersion  time
          and clay fraction because of effects due to seawater.

     (3)  Adsorption  of  lead is  about 80% regardless of  both immersion  time
          and clay fraction.

EFFECTS OF  CLAY TYPES ON ADSORPTION OF HEAVY METALS

     In  this  experiment,  the  difference  in  adsorption by types  of  clays was
investigated.   Six kinds  of  clay,  shown in Table 1, and coral sand  from Okin-
awa were used.   For the purpose of a precise comparison, all  clays were sieved
through  0.074  mm  mesh and  artificial seawater was   used.   The  experimental


                                     217

-------
method is  the same  as  described for  the  sand experiments.   Results  of this
experiment are shown in Table 2 and  may be  described as follows:

     (1)   Generally,  adsorption of  heavy  metal  increases  in proportion  to
          turbidity.  But the  influence  of a pH change on adsorption of heavy
          metal  is not clear.

     (2)   The percentage of  mercury  adsorbed is higher than  that  of lead and
          that of cadmium.

     (3)   Heavy  metal  is  more easily adsorbed  on coral  sand than on  clay.
   TABLE 2.   ADSORPTION OF HEAVY METAL TO DIFFERENT KINDS OF CLAY IN JAPAN
Clay Type
Aomiri

Kawasaki

Nagoya

Fushiki-
Toyama
Kobe

Moji

Okinawa
(coral sand)
%
pH
%
pH
%
PH
%
pH
%
PH
%
pH
%
pH
Metal

cc
oo
(ppm) 20
-
4.3
-
4.1
0
4.2
-
4.3
-
4.0
-
4.0
-
6.5
Lead


200
-
4.8
6
4.9
-
4.4
-
4.6
3
5.0
-
4.4
88
9.3



2000
91
5.6
99
6.6
84
6.0
46
5.8
99
7.2
97
6.7
99
9.5
Cadmi urn


20 200
0
5.2 5.6
6
5.5 6.2
1
5.1 5.4
1 4
5.1 5.5
0 11
5.3 6.4
2 0
5.3 6.1
7 12
9.0 9.6



2000
11
5.5
62
6.9
32
5.3
5
6.2
83
6.3
40
7.0
74
9.7



20
36
5.4
36
5.5
2
5.4
10
5.1
9
5.3
32
5.3
94
8. 1
Mercury


200
70
5.1
93
6.3
90
5.8
95
5.7
93
6.4
92
6.1
89
9.6



2000
98
5.8
90
6.8
97
6.5
85
6.3
98
6.4
92
7.1
70
9.7
                        EXPERIMENTS ON SAND FILTRATION

FILTERING EFFECT ON BACKFILL SAND

     The absorption experiments  show  that heavy metal is adsorbed to clay and
that the percentage of  adsorption depends on the kind of clay, kind of water,
pH  of  the  solution,  turbidity  and  other  factors.   If the  clay  particles,
including heavy metal and  other contaminated substances, remain  in  the back-
                                      218

-------
fill sand while  water  permeates  through the sand,  secondary  pollution in the
vicinity can be minimized.

     The purpose of  this  experiment was to  investigate  the  filtering capacity
of  sands  used for  backfilling.   The experimental  apparatus  consists  of  two
cylinders as  shown  in  Figure  9.    Kawasaki  clay,  Takahagi sand,  and Toyoura
sand were  used  for  the filter media.   Factors  such as  concentration of the
suspension,  water  pressure,  thickness  of sand, kind of sand and kind of water
were tested.  The results of this experiment are

     (1)  The  filtering effect of  the  sand changed with time  until  the sand
          finally  became  impermeable  due  to  clogging  by  clay  (Figure 10).

     (2)  In  the Toyoura sand, which  has  a  small  grain  size,  the filtering
          effect is nearly total.

     (3)  The  clay  particles  flocculate  in seawater  and thus  the filtering
          effect of sand becomes more pronounced  than in freshwater.

     (4)  The most  important  factor seems to be  the grain size of sands, that
          is,  if  the  grain size  is  smaller,  the  filtering effect  is more
          significant.

     (5)  Any  noticeable  difference in filtering effects due  to factors such
          as water  pressure,  thickness  of sand layer and concentration of the
          suspension was not found.

EFFECTS OF GRAIN SIZE OF SANDS ON FILTRATION

     The  purpose  of  this  experiment  was  to  investigate  the effect  of sand
grain  size  on the  efficiency  of filtering  solutions  with heavy  metals.   In
preparing test samples, careful attention was paid to adjusting the grain size
of  sands  and  clays.   Kawasaki  clay, Takahagi sand and Toyoura sand were care-
fully  sieved.  A cylinder  (d = 10  cm,  h  = 70 cm) was kept at 500 ppm and the
water  head was kept at  60 cm.  The filtration time was 1 hour.  In considering
the relative  influence  of  grain  size of sands to that of clays, the clay-sand
ratio,   R  (d/D10) is defined as the ratio of the  maximum grain size of clay, d
=  0.074 mm, to  the effective grain  size of  sand,  D10.  The  experiment was
carried out  by  changing this ratio, R.   Figure  11  shows the  results of these
experiments and  from this it is apparent that the filtering effect does depend
on the clay-sand ratio, R,  and is about 100% effective when R  >_ 0.2.


                 PERMEABILITY TESTING OF SEALS FOR PILING JOINTS

     In Japan,  several  kinds of  seals  have been used to make  the joints be-
tween  sheet piles watertight.   These  seals are  classified  into  four types:
mortar, asphalt,  urethane  and  cellulose.   Since  information on the permeabil-
ity of conventional mortar  seals is  available,  the permeability  tests were
performed on  the other three types of  seals.  Urethane and cellulose work as
sealing materials by swelling.   Asphalt simply fills the joints.
                                      219

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-------
     The apparatus and results  are shown in  Figures  12  and  13.   From Figure 13
it is clear that the coefficient of permeability,  K,  is on  the  order of 10-3  N
10-4 cm/sec and  increases  in  proportion to  the  water pressure.   For practical
use of these  results,  further  investigations  on the durability  of  seals  with
hot water and other substances  are necessary.


                                  CONCLUSIONS

     Several series of experiments were conducted  to  investigate the filtering
effect of  containment walls for  landfills  with dredged materials.   From the
experimental results, it was concluded that:

     1)   Adsorption of heavy metals  (such  as mercury, cadmium, and  lead) to
          clay increases in proportion to turbidity.

     2)   Adsorption of heavy metal  to clay is  greater in  alkaline solutions
          than in acid solutions and this tendency is more  notable  for cadmium
          and lead.

     3)   Cadmium is not adsorbed on clay in seawater.

     4)   Clay  particles  produce  floes in  seawater  and  are   deposited  more
          rapidly than in freshwater.

     5)   Heavy  metal  is  adsorbed on  clay in  sands  in  the  same  way as in
          suspension.

     6)   Clay samples taken in  the main ports  of Japan had  similar physical
          and chemical properties; hence they  showed  a  similar  tendency toward
          adsorption of heavy metals.

     7)   The  filtering  effect  of sand  depends  on the  clay-sand  ratio,  R,
          defined as  the  ratio  of the maximum grain size  of  clays, d = 0.074
          mm to  the  effective  grain size of sands,  D10 and is  nearly 100% for
          R > 0.2.

     8)   It  is  expected  that  backfill  sand  has  a  filtering effect  which
          prevents the permeation of contaminated  substances.

     9)   Seals  used for  making  watertight  joints  between  sheet  piles are
          useful  in  preventing  permeation.   When  seals are used the coeffic-
          ient  of permeability,  K,  is on  the  order  of 10-3  N 10-4  cm/sec.

     Although useful data were  obtained on prevention of permeation of contam-
inated  substances,   it  is  necessary  to  continue  the  research because  many
problems remain unsolved regarding long-term permeation, the permeation veloc-
ity  of  contaminated  substances  and the influence of  tides and  earthquakes.
                                     222

-------
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                    WATER  PRESSURE P (kg/cm2)
Figure  13.
  Relation between  coefficient of  permeability  K and water
  pressure.
                                223

-------
                        ACCUMULATION OF MERCURY BY FISH
                          FROM CONTAMINATED SEDIMENTS


              R.  Hirota,1 M.  Fujiki,2 Y.  Ikegaki3 and S.  Tajima2


                                   ABSTRACT

     The relationship between body length and mercury concentration in fish is
not known  for  fish  that inhabit areas of  the  sea bottom sediments containing
mercury.    Fish captured  from Minimata  Bay where  there is  a great  deal  of
mercury pollution and  uncontaminated fish  grown in pens  in  Minamata  Bay were
studied to determine  if there was a  correlation  between  accumulation of mer-
cury in fish flesh and rearing time in Minamata Bay.

     The correlation coefficients (r) between the concentration of accumulated
mercury and body  length were 0.676 for common seabass, 0.65 for marbled rock-
fish,  0.63 for jack mackerel, 0.61 for black sea bream, and 0.35 for rockfish.
These   are  considered statistically  significant.  Correlation  coefficients of
0.3 for red sea bream, 0.096 for the common nibbler,  and -0.06 for mullet were
not statistically significant.

     Fish were separated  into four groups  and  reared  in  pens  at two  stations
in Minamata Bay.  The  tendency for mercury accumulation  in  the fish  from the
different experimental groups was different for each  species.

     From the results it appears that selected species and ages of fish should
be  used  when  a  mercury  monitoring  program is  implemented in  Minamata  Bay.


                                 INTRODUCTION

     More than seven years have passed since a chemical factory, using mercury
as a catalyst, stopped  discharging its effluent  into  Minamata Bay.   However,
the bottom sediment  of  the bay still contains  mercury.   It is estimated that
over 25 ppm  of mercury—more than 1.5 million m3 contaminates the bay's sedi-
ments.   The  highest concentration  of mercury  has been  reported  at  262 ppm.

     It is known  that the mercury accumulated  in fish gradually increases in
proportion to  body  weight as the fish grows older.   However, no investigation
of the exact  relationship between the concentration  in  the  fish and  the body
 1  Aitsu Marine  Biological  Station,  Kumamoto  University,  Kumamoto,  Japan.
 2 Institute of Community Medicine, the University of Tsukuba,  Ibaraki,  Japan.
 3 Assistant Chief, Environmental Department, Kumamoto Prefectural Government,
  Japan.
                                     225

-------
weight had  been done  for  fish  living  in the  sea  where the  bottom sediment
contained mercury,  such as in Minamata Bay.

     Since  1973 the  government  of Kumamoto  Prefecture has  investigated  the
concentration of mercury  in  fish captured from Minamata Bay,  and it has also,
since 1975,  been investigating the relationship between the mercury concentra-
tion  in  red sea bream, common nibbler and marbled rockfish  and  rearing time
for fish reared in the pens at Minamata Bay.

     This paper reports on  the results obtained from  statistical  analysis  of
the data derived from these investigations.


                             MATERIALS AND METHODS

INVESTIGATION A

     Fish captured  from Minamata  Bay  were used for  the  investigation.   The
body  length  and concentration  of mercury in the muscle of fish were measured.
Flameless atomic absorption spectronhotometric techniques we^e used to analyze
the total mercury in the fish muscle.

     Rockfish,   red  sea  bream,  common  nibbler, mullet,  common seabass, marbled
rockfish, jack mackerel and black sea bream were selected as test species from
the  many kinds  of  fish—mostly  because  these were  captured in  sufficient
numbers for statistical analysis.  Correlation coefficients (r-values) between
the concentration  of the  accumulated  mercury and body  length  were determined
for the above eight species of fish.

INVESTIGATION B

     Red sea bream  grown  from eggs in a  fish farm  at Oyano Marine Station in
Kumamoto Prefecture  and marbled  rockfish and  common  nibbler  captured  in  the
field  were   used  in  the  investigation.    The  fish  were separated  into four
groups and  were reared in pens  at the  two stations in  Minamata  Bay shown  in
Figure 1.   The rearing period was as  follows: Group A:  red  sea bream  and
marbled  rockfish   were reared  from  July 1975  to  December  1975.    Group  B:
common nibbler  were  reared  from December 1976 to May 1977.   Group C:  red  sea
bream and common  nibbler  were reared from June 1977  to November 1977.   Group
D:   red  sea bream  and common nibbler  were  reared  from November  1977  to  May
1978.

     Ten fish from each group were taken from the pen every 10 days during  the
rearing period and the concentration  of total  mercury in the muscle tissue  was
measured using  a  flameless atomic absorption  spectrophotometer.   Using these
data, the relationship  between rearing time and accumulated  mercury was stu-
died.
                                    RESULTS

     The  results  of  Investigation A  are  in Table  1.   The  concentration  of
accumulated mercury  in common  seabass  and marbled  rockfish showed  0.41  ppm


                                      226

-------
                 KOIJI ISLAND
                                               t.;MIDORIURA


                                               &TSUKINOURA
                                               $y.:. ;--. ;  •

                                           ••'.-YUDOO'- •   ' '
                 Figure 1.   Rearing pen sites in Minamata Bay.
(wet  weight)  and  0.85 ppm  (wet  weight),  respectively.   These  values  were
higher than the Japanese government's provisional criteria for mercury in fish
of 0.4 ppm (wet weight).

     The  statistically significant  correlation coefficients  between accumu-
lated mercury and body length were 0.676 for common seabass (p ซ 0.001), 0.65
for marbled  rockfish (p ซ  0.001),  0.63  for  jack mackerel  (p  ซ  0.001, 0.61
for black  sea  bream  (p ซ 0.001) and 0.35 for rockfish (p < 0.001).  Correla-
tion  coefficients  (r-values) of  0.3 for red  sea bream  (p  <  0.1), 0.096 for
common nibbler (p < 0.3) and -0.06 for mullet (p < 0.6) were not statistically
significant.

     For the eight species of the fish, scatter diagrams for the concentration
of accumulated mercury vs body length are given in Figures 2 to 9*

     The results of  Investigation B are shown in Figures 10 to 13.  For group
A, the concentration of mercury in red sea bream increased gradually, although
that  of  marbled  rockfish did  not increase during  the  rearing  period.   For
group B, the  concentration  of mercury in the  common  nibbler increased a lit-
tle.   For  group C, the concentration  of  mercury in red  sea  bream and common
nibbler  did  not increase.   And  for group D,  the  concentration  of mercury in
red sea bream and common nibbler increased gradually.
                                  DISCUSSION

     It is  important  to  monitor water quality  so  no further pollution of the
marine environment  is  caused by the dredging which will clean up pollution in
Minamata Bay.   If mercury elutes from the bottom sediment to the marine water,
^Figures 2 through 13 are found at the end of the text, beginning on page 230.

                                      227

-------
TABLE
CORRELATION OF ACCUMULATED MERCURY AND  BODY  LENGTH  IN  FISH
                     Rockfish  Red sea  bream   Common  nibbler
                                                      Mullet
                    121
                        27
  129
85
Body length
(cm)
Total mercury
(ppm)

Regression line
X
Sx
y
sy
r
t
d.f.
P

15.615
2.51
0.2255
0.0850
0.35
4.093
119
<0.001
y=0.012x
+ 0.04
12.9
4.51
0.231
0.135
0.3
1.778
25
<0.1
y=0.0009x
+ 0.23
18.767
3.760
0.1256
0.043
0.097
1.100
127
<0.3
y=0.0011x
+ 0.105
32.66
5.200
0.045
0.032
-0.06
0.529
83
<0.6
y=-0:-00004x
+ 0.045

         Common seabass  Marbled rockfish  Jack mackerel   Black sea  bream
              114
                     133
133
97
Body x
length Sx
(cm)
Total y
mercury Sy
(cm)
r
t
d.f.
P
Regression
1 ine
36.803
11.034
0.4125
0.3561
0.676
9.712
112
ซ0.001
y=0.0217x
- 0.387
14.747
2.29
0.8488
0.3179
0.65
9.842
131
ซ0.001
y=0.091x
- 0.5
21.604
6.309
0.1379
0.0938
0.63
9.236
131
ซ0.001
y=0.0093x
- 0.06
21.89
5.228
0.384
0.4308
0.610
7.497
95
ซ0.001
y=0.0495x
- 0.70
                                 228

-------
or if the  concentration  of mercury in marine food products is increasing,  the
dredging must be  slowed  or stopped unt.il  the cause of the pollution is deter-
mined.    To support  the  monitoring plan,  the baseline  condition  of  fish  in
Minamata Bay must be established before dredging begins.

     The results  presented  in  this paper show that  the  concentration  of mer-
cury in  common  seabass,  marbled rockfish and some  of  the black sea bream was
higher  than  the  Japanese   government's  provisional criteria for  mercury  in
fish.    This  suggests  that Minamata  Bay  is  still  polluted  by mercury  when
compared to other areas.

     Correlations between  the  concentration  of  accumulated  mercury and body
length  were  statistically   significant  for  common  seabass, marbled rockfish,
jack mackerel,  black  sea bream and rockfish.   The concentration of mercury in
the above five species of fish  increases in proportion to the  age of the fish.
The presumed ages of common seabass, marbled rockfish and jack mackerel were 1
to 7 years old and black sea bream was 1 to 5 years old for those fish  used in
the  investigation.    The   correlation  coefficients  between  body   length  and
concentration of accumulated  mercury  in  red sea  bream,  common  nibbler  and
mullet were not  statistically  significant.   This may be  because the  presumed
age of  red sea  bream was 1 year old.   Another reason for the  lack  of correla-
tion between the  concentration of accumulated mercury and body length  is that
rates of mercury uptake in common nibbler  and mullet  are  low and rates  of
excretion from these fish are high.

     The studies  of accumulation  vs  rearing time  showed  no  relationship  be-
tween the experimental groupings of fish.   The accumulation of mercury  in fish
may be  lower  than the statistical deviation  of  the level  of  concentration of
mercury  among fish  because the rearing period was only 6 months.   There was a
slight  accumulation exhibited  by  the  marbled  rockfish  and  common  nibbler.
                                  CONCLUSION

     This investigation suggested that certain species and ages of fish should
be  identified  as bio-monitors  to  signal any increased  pollution  in  Minamata
Bay.  Jack mackerel  and black sea bream would be good species for a monitoring
effort because these  have  the highest correlation between body length and the
concentration  of accumulated  mercury  in  muscle  tissue.   Also,  the  present
concentration of mercury  in  muscle tissue of these  fish is  below the govern-
ment criterion of 0.4 ppm.
                                      229

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                                     236

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              APPROACHES FOR MITIGATING THE KEPONE CONTAMINATION
                 IN THE HOPEWELl/JAMFS RIVER AREA OF VIRGINIA

                       K.  M. Mackenthun, M.  W.  Brossman,
                          J. A.  Kohler, C.R.  Terrell
                        Criteria and Standards Division
                     Office of Water and Waste Management
                     U.S.  Environmental Protection Agency
                            Washington, D.C.   20460
                                   ABSTRACT

     The  Kepone  Mitigation Feasibility  Project  discussed at  the  third U.S./
Japan meeting  on management  of  bottom  sediments  containing  toxic substances
has  been completed.   The four-volume  project  report  was  forwarded  to  the
Governors of Virginia  and Maryland,  together with a  recommendation  of forma-
tion of  a task force to consider and implement the report's recommendations.

     This  paper   summarizes   the  nature  of  the contamination  found  in  the
Hopewel1/James River  area and describes the mitigation  approaches  evaluated
and the  mitigation actions  recommended.

     Extensive sampling efforts revealed the highly persistent Kepone contami-
nation remains on the land in Hopewell,  in sewage lines and streams and in the
James River.  Accordingly, mitigation methods  had to focus on the problems of
land, water and  sediment  contamination.   Conventional  (dredging),  non-conven-
tional,  and degradation/biological approaches to mitigation were investigated.

     The  investigation  of  conventional  mitigation/removal  approaches included
an analysis of world-wide dredging  techniques,  with an evaluation of the most
promising  dredging   techniques  for  removal  of  contaminated  sediments  from
specific  sites,  engineering  studies  to  contain,  stabilize or remove contami-
nated sediments at points of inflow into the James River and evaluation of the
engineering requirements for removal  of Kepone-contaminated sediments from the
James River,  assessment of  dredge  spoil sites, fixation of  the  dredge spoil
and treatment  of  the elutriate.

     A wide range of  non-conventional  mitigation approaches  was evaluated for
dredge spoil  fixation,  elutriate  treatment, in situ stabilization, and isola-
tion.  Approaches  ranged  from silicate,  organic- and  sulfur-based fixation
agents  through   use  of retrievable and  non-retrievable sorbents  which would
take up  Kepone from the contaminated sediments and water.

     Natural  degradation  and  biological  mitigation approaches were examined
concurrently with  engineering approaches.  However,  none  of  these approaches
shows high promise for Kepone mitigation at this time.


                                     241

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     As a  result of  these  investigations, a  number of  immediate  mitigation
actions  were  recommended   in  addition  to further  development of  promising
mitigation  techniques.    Among  the  recommendations was  the  adaptation  of
Japanese dredging and sediment fixation technology.  In  addition,  the investi-
gative techniques and findings  were recommended for solution of other similar
waterway contamination problems  in the United States.

                                 INTRODUCTION

     At the  third U.S./Japan  meeting  on management of  bottom  sediments con-
taining toxic  substances a  paper  was presented,  "Mitigation  Feasibility for
the Kepone-Contaminated  James  River,  Virginia"  (1).   That paper described the
origin of  the Hopewel I/Virginia Kepone  contamination,   the  study  approach to
assess  the  problem,  preliminary findings  on  the  nature  and  extent  of the
contamination  and  the   specific  conventional  (dredging)  and  unconventional
approaches  under investigation  to  mitigate  the  problem.   The study  is now
completed  and  the  four-volume  project  report  has  been  provided  to  the
Governors of Viginia and  Maryland.

     This paper  is  devoted primarily  to  characterizing  the  nature of the
contamination found,  techniques  evaluated  for mitigation of the contamination
problem and  the  specific recommended  mitigation  actions.   Additional  details
may be found in the Kepone Mitigation Project Report (2).

                          NATURE OF THE CONTAMINATION

     Kepone,  a  highly chlorinated  hydrocarbon  pesticide,  was  discharged into
the environment  around  Hopewell, Virginia  from 1966 to  1975 from two manufac-
turing operations.  The  Allied  Chemical  Corporation's  Semi-Works  Plant pro-
duced Kepone  intermittently  from 1966 to  1974.   Life Science Products Company
began  Kepone  production under  contract  to Allied  Chemical  in  1974 and con-
tinued  production  until  closure of  the plant  in  September 1975.   Fish and
sediment samples  indicate Kepone contamination  existed   in the  James River as
early  as  1967.   Figure  1  shows the  principal  landmarks  around  the Hopewell
area which  will  be  cited in the discussion  of  the contamination and remedial
actions.

     Ear.ly warnings of Life  Science Products careless manufacturing and dispo-
sal practices  were apparent with  the malfunctioning of the digesters  of the
Hopewell  sewage  treatment  plant and  the  deleterious  health  effects  on the
production  workers.   Subsequently,  the finding  of high  levels  of  Kepone con-
tamination in James River fish brought about a ban on fishing for a wide  range
of species.   The  releases from the  Life Science Products plant into the envi-
ronment were  associated  with atmospheric emissions, wastewater discharges and
bulk  disposal  of off-specification batches.   The atmospheric  emissions from
the plant  settled on the  surface   soils.   Wastewater discharges  entering the
sewage system passed  through the Hopewell   sewage treatment  plant  into Bailey
Creek, passing into Bailey  Bay and the James River.  Disposal  of off-specifi-
cation batches and  manufacturing residues  of Kepone occurred at  a minimum of
two sites-the Hopewell  landfill  and the disposal trench  at the former Pebbled
Ammonium Nitrate Plant.  Following  closure of Life Science Products, residues
from the dismantled plant and site cleanup were buried at the landfill.
                                     242

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                                                          243

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Drummed  residues  from  Kepone production  were stored  at  te Hopewel1  sewage
treatment plant and  at  Portsmouth,  Virginia.   Kepone-contaminated sludge from
the Hopewel1 sewage  treatment plant was stored in a lagoon constructed at the
sewage treatment plant site.

     Almost three-years following  the  closure of  the  Life  Science  Products
plant, the disposal  of  the drummed Kepone production residues and the Kepone-
contaminated sludge  is  unresolved.   Several   sites in  the  City  of  Hopewell
contain Kepone; small inflows of Kepone continue into the James  River, and the
levels of  contamination remain sufficiently  high  in the 110 km  of  the river
from  Hopewell  to  the mouth  to  cause  continued closure  of the James  River to
recreational  and  commercial   fishing  for  many species of  fish and shellfish.
Table  1  summarizes  the  estimates  of Kepone  residuals  in the  Hopewel1/James
River area.
                    TABLE 1.   ESTIMATE OF KEPONE RESIDUALS
      Residing In
                                            Estimated Quantity of Kepone
                                  Ib
Sewer System
Surface Soil (1 inch)
Kepone Sludge Lagoon
Bailey Bay Sediments*
James River Sediments*
Drums at Hopewell
Drums at Portsmouth
Landfill!
Pebbled Ammonium Nitrate
  Plant Site
Rounded total*
       23
    45 - 450
      100
   540 - 2,000
 9,000 - 17,000
     9,400
    13,000
     1,400

      100
33,700 - 43,600
       50
   100 - 1,000
      220
 1,200 - 4,300
20,000 - 38,000
     20,700
     28,800
      3,100

      220
73,500 - 95,500
*  Low value reflects estimate extrapolated from mean concentrations, high
   value reflects estimates based on mean plus one standard deviation.

t  Includes identified deposits only.


                  CONVENTIONAL MITIGATION/REMOVAL APPROACHES

     The project  investigation of  conventional  mitigation/removal  approaches
included:  (1)  site  surveys,  analysis of world-wide  dredging  techniques, and
assessment of  the  most  promising dredging techniques for  removal  of contami-
nated  sediments  from  specific  sites;  (2)  engineering  studies to  contain,
stabilize or remove Kepone-contaminated sediments at points of inflow into the
James River, together with an assessment of their effectiveness and potential
environmental  impacts;  and (3) evaluation of the engineering requirements for
                                     244

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removal  of  Kepone-contaminated  sediments  from the James  River,  assessment of
dredge spoil  sites,  fixation of  the  dredge spoil,  and treatment  of  the  elu-
triate.

     The majority  of these  efforts  were  carried out by  the  Norfolk  District
Corps of Engineers for  the Kepone Project  Office and  are described in detail
in Appendix B  of EPA's Kepone Mitigation Feasibility Report (2).

DREDGING TECHNOLOGY ASSESSMENT

     The evaluation  of  world-wide  dredging  technology  involved a survey of
mechanical, hydraulic and  pneumatic  dredges.   The most common  dredges  in the
United States are  the  mechanical  and  hydraulic  type.  Table  2  summarizes the
characteristics of the  major types  of mechanical and hydraulic dredges in use
in the United  States.

     Often   considerable  turbidity is  generated  in  the use of  these  dredges.
Accordingly, when dredging contaminated sediments, such dredges pose a serious
threat through secondary pollution.   To control this  problem,  various  types of
silt curtains and turbidity barriers  have been devised with varying degrees of
success.   Conventional  hydraulic  dredges  pose additional  problems in  handling
contaminated  sediments   since   they  collect  only 10  to  30  percent  solids.
Disposal  of dredge spoil  can induce  secondary pollution from runoff or leach-
ing  from  the  dredge spoil  site, or  impose  high costs  in  treatment  of the
elutriate  at  the  dredge spoil   site prior  to  return  of the liquid  to  the re-
ceiving water.

     Dredging technology in Europe is generally similar to the capabilities in
the  United  States.   However, special  purpose dredges  have  been devised.  Of
these, a pneumatic dredge,  the  Pneuma dredge  developed  in  Italy,  has special
advantages   in handling  contaminated  sediments.  The advantages  of the Pneuma
include minimum  wear,  continuous flow,  limited  secondary pollution  and  high
solids removal—60  to  80  percent solids by  volume.   The  Pneuma dredge,  how-
ever, is only practical  for removal  of sediments at  considerable depth as the
hydrostatic pressure of water is required to move the sediments into a chamber
from  which  the material is  expelled  through  a pipe  to a  containment  site by
compressed  air.

     Japanese dredging  technology for  handling  of contaminated  sediments is
considerably  advanced over  that in  the United States.  Table 3 summarizes the
characteristics of the major types of  dredges  developed in Japan.  Analysis of
the  characteristics  of  these dredges and a site survey of operations  in Japan
indicated that the Oozer dredge does  not require hydrostatic  pressure  to force
the  sediment  into  its  chambers*.  The Oozer  dredge utilizes  a  vacuum to draw
the sediment  into  its  chambers,  subsequently  discharging the dredge spoil
     Comprehensive  side-by-side  comparisons of  potentially  promising dredges
     operating under James River conditions do not exist.  However, testing of
     the Oozer  dredge in the  James  River would at a  minimum  provide on-site
     operating parameters for evaluating competing systems.
                                     245

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               TABLE 2.   MECHANICAL DREDGES IN THE UNITED STATES
   Type of
   dredge
                     Method of operation
Dragline
Dipper
Grab
Endless
Chain
(bucket
ladder)
Contains scoop that is lowered into
  water and slices material  to be
  removed as scoop is drawn  toward
  dredge.
)
Contains shovel  that is lowered into
  water and slices material  to be    )
  removed as shovel is drawn away    )
  from dredge.                        )
Scoop, shovel,  or
clamshell is
lifted by crane
and dredged
material is depo-
sited either on a
barge or on the
bank.
Contains grab or clamshell  bucket.    )
  Material is removed by forcing     )
  opposing bucket edges into it.      )
  Bucket is then closed.              )

Includes endless chain of buckets.   Material  removed by
  forcing single cutting edge of successive buckets into
  material.  Material deposited in barge or other
  conveyance.
                    HYDRAULIC DREDGES IN THE UNITED STATES
Cutterhead



Plain Suction

Dustpan



Hopper
Sidecaster
Rotary blades cut into bottom material.   Centrifugal  pump
  removes material with dilution water and transports it in
  a pipeline to disposal area.

Operates same as cutterhead but without rotary cutter.

Material removed with water jets and picked up with dilution
  water by a wide but shallow suction inlet, pumped through
  discharge line, and returned into water adjacent to channel

Dredge equipped with suction pipe, draghead, and hoppers or
  bins that store hydraulically dredged material.   There is
  no pipeline.   Disposal is either at sea or pumped into a
  disposal site at the pier.

Material picked up with dilution water and pumped back
  directly into adjacent waterway, a distance from the
  channel.
                                     246

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                     TABLE 3.  DREDGES DEVELOPED IN JAPAN
   Type of
   dredge
Method of operation
Clean Up          Looks like a conventional hydraulic cutterhead except for
                    clean-up head installed on ladder.  Head is equipped with
                    a movable wing or shield to overlie bottom sediment, a
                    movable shutter plate, an auger, a device for collecting
                    gas, and sonar devices to indicate elevation of material
                    before and after dredging.

Anti-turbidity    Overflow system on hopper dredges is designed to have turbid
                    water (slurry hopper dredges mixture) that is discharged
                    overboard quickly submerged.   Discharged slurry settles
                    rapidly to the bottom instead of remaining suspended in
                    the water column.

Oozer             Comparable to Pneuma pump in utilizing water pressure to
                    raise material to be dredged.  In addition suction is in-
                    creased by creating a vacuum in the tank.  After material
                    has filled tank, compressed air forces sludge to be dis-
                    charged.   Transports sludge in high density and without
                    causing significant turbidity.   Well suited for removal
                    of viscous sediments.

Watertight        Closed type.   Especially designed for dredging without giving
Grab Bucket         rise to secondary pollution when used for dredging settled
                    sludge.
under air pressure directly by pipeline to a dredge spoil site or barge.  This
dredge is capable  of  removing dredge spoil with high solids content, operates
at  minimal  draft,  effectively controls  secondary  pollution,  and  has shown
minimal  operational  difficulties under a range of sediment conditions.

ENGINEERING STUDIES TO CONTAIN CONTAMINATED INPUTS INTO THE JAMES RIVER

     Engineering approaches  for  preventing continuing  inflows of  Kepone con-
tamination  into  the  James  River  were  investigated.   Eighteen  engineering
alternatives were  proposed and evaluated.  These  alternatives considered the
feasibility and utility of checking Kepone contamination from Bailey Creek and
Gravelly Run which  discharge  into Bailey Bay,  as well as removal  and contain-
ment of  contamination from Bailey Bay which discharges  into the James River.

     The alternatives were  limited to structural  solutions  such  as dredging;
various   types  of  levee,  dam  and wall  construction; channel improvement  or
modification;  covering or  sealing;  and  other combinations  of structural solu-
tions.   The analysis included an  investigation  and evaluation of  the engineer-
                                     247

-------
ing  feasibility,  implications,  and cost for  removing  the Kepone-contaminated
sediments  from  Bailey Bay  and  Bailey Creek  areas.  Based  on  related project
efforts,  it  was concluded  that  implementation of most  of  these alternatives
was  viable only  if complete cleanup  of the  James  River  were  contemplated.
However,  two  of the  alternatives  offered potential  utility and  benefits  as
dredge spoil  sites in Bailey Bay for currently contemplated maintenance dredg-
ing.

ENGINEERING STUDIES FOR REMOVAL OF KEPONE FROM THE JAMES RIVER

     Both  complete removal  of  Kepone-contaminated  sediments  from  the  James
River  and partial  removal   of  contaminated  sediments  from "hot  spots"  were
evaluated.  Figure  2  illustrates key physical features of the area.

Complete Removal

     Complete  removal  of contaminated  sediments  would  involve  approximately
110  kilometers  (69 miles)  of  river from Hopewell to  the mouth.   These  sedi-
ments are generally characterized as silty clay,  less  than  64 microns.

     The  parameters  and  conditions  considered  in the  analysis  of full-scale
removal  of sediments  from  the  James  were  as  follows:   excavation  would  be
limited to the  James  River from Hopewell to the James River Bridge (no dredg-
ing  was  considered in tributaries  of the  James);  excavation depth would  be
limited  to 38  centimeters;  disposal  be limited  to  adjacent  sites;  sand for
disposal  area  construction  would  be within an  economical  pumping  distance  of
each  site; the  Oozer dredge  would  be  available;  approximately   25  percent
excess material would  be removed due to over-dredging; and the Oozer pipeline
has a capability to pump material 1,524 meters  (5,000 ft).

     Thirteen disposal areas were  proposed for confinement of Kepone contami-
nated  spoil.  Preference was given  to sites  contiguous  to  the  shore and care
was  taken to  select  locations  that  would   have  minimal  impact  on adjacent
drainage  patterns.   Some   filling  of  interior  low  areas  was  anticipated.
Design  levels,  based  on  100-year  flood  level,  dictated  an  elevation  of  3
meters  (10 ft) above  sea  level  datum.  Areas  not utilized to  capacity  would
provide dredge spoil sites for future maintenance dredging.

     The  results  of this analysis  are shown  in Table  4.   Removal  of 133 bil-
lion cubic meters  (169  billion  allowing a 25 percent  excess)  of material and
disposal would cost approximately $1 billion.

     If elutriate  treatment and spoil fixation  costs are considered, the total
cost  of  the project  would range from  $1  to  $7.2  billion, depending  on the
treatment  chosen.   Elutriate   treatment  costs  for   ultra-violet/ozone  were
calculated considering a portable  UV/oxone unit and a treatment rate of $.067
1,000  liters  ($0.23/1,000  gallons),  excluding  logistics  or capital  costs  or
possible  water clarification costs.   A summary of a  complete  treatment  costs
estimate  for  treating the  James River sediments  with  intra-basin  disposal  is
presented in Table 5.
                                     248

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                                                                    NORTH
                                                                    CAROLINA
TOPPAHANNOCK
                                                                   LOCATION MAP
                                                                   40   0   40 MILES
                                                           CHESAPEAKE
      RICHMOND
HOPEWELL
          PRINCE GEORGE
               CO     .
                                                v  AHAMPTON
                                               PORTSMOUTHYf. '-TV VIRGINIA
                                                     '•'..•;  Sf     VN- BEACH ' -
                                                    CHESAPEAKE-.  . ;
        NORTH CAROLINA
                                                      NORFOLK DISTRICT CORPS. OFENOINEERS- SEPT. 1977
                    SCALE IN MILES
                                       Figure 2.
                                          249

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      TABLE  4.   SUMMARY  FOR  CONVENTIONAL  REMOVAL OF  KEPONE CONTAMINATED SEDIMENTS IN THE JAMES RIVER

Disposal
Areas
1
2
3
4
5
6
7
8
9
10
11
12
13
TOTALS


Acres
444
560
248
411
276
767
736
907
533
872
1572
1635
725
9766


Elevation of
Slurry mse
10.4
10.3
7.1
8.9
8.4
6.7
5.4
7.4
9.3
7.5
10.4
9.2
8.4
ROUNDED


Dredged Qual ity
15" depth
7,440,000
8,610,000
2,790,000
6,740,000
5,050,000
10,440,000
12,830,000
18,440,000
11 ,300,000
14,260,000
37,780,000
28,460,000
12,780,000
176,920,000
(177,000,000)


in Cubic Yards
25%
Excess Included
9,300,000
10,762,500
3,487,500
8,425,000
6,312,500
13,050,000
16,037,500
23,050,000
14,125,000
17,825,000
47,225,000
35,575,000
15,975,000
221 ,150,000
(211 ,000,000)

ROUNDED
Dredging Costs
at $4. 30/cu yd
for 15" depth
$31 ,992,000
37,023,000
11 ,997,000
28,982,000
21 ,715,000
44,892,000
55,169,000
79,292,000
48,590,000
61 ,318,000
162,454,000
122,378,000
54,954,000
$760,756,000
$761 ,976,000*
(762,000,000)
Disposal Site
Preparation Cost
$3,550,000
4,480,000
7,610,000
11 ,990,000
11,050,000
9,200,000
15,110,000
15,340,000
13,950,000
11 ,620,000
17,380,000
20,200,000
10,840,000
$153,120,000
$220,490,000*
(220,500,000)
                       Total  Cost for Dredging  and  Disposal  Including  Contingencies
                          Engineering and Design  Studies  and Administrative  Costs
              Total  Project Costs

                 $902.5 x 106

                  $1  billion
Total  Dredging Cost

    $762 x 106

      Rounded
Total Disposal Cost

   $220 5 x 106
                      (Total  removal  and disposal  costs  amount  to  $5.55/cubic  yard.)
*Total  cost includes contingencies,  engineering  and  design  studies  and  administrative  costs.
                                                   250

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     Battelle Pacific Northwest  Laboratories,  in separate efforts, determined
costs and  some  environmental  consequences  for other i_n situ mitigation propo-
sals. These  results are also included in Table 5.

MITIGATION THROUGH CLEANUP OF ELEVATED AREAS OF CONTAMINATION

     Certain areas  of the  James  River contain  more Kepone than  others  as a
result  of the  discharge patterns  and hydro!ogic  influences.   For  example,
Bailey  Bay sediments  contain  up  to  10 ug/g (ppm)  of  Kepone as  a  result of
proximity  to the discharge source at Hopewell.  Concentrations of the order of
1  |jg/g (ppm) of Kepone are contained in the sediments of the turbidity maximum
zone as  a  result  of estuarine hydrologic  influences.  The  Battelle  model  was
utilized to evaluate the effectiveness of partial  clean-up.

     Ten selected zones of high Kepone sediment contamination were designated.
The  local  effects of  cleanup  were  assessed  as well  as  the  effect  near the
mouth of  the James  River discharging into  Chesapeake  Bay.   Results  were  com-
pared with the  no-cleanup  case for total,  dissolved and suspended particulate
Kepone  (attached  to sediments).   The  model results  indicated essentially no
improvement  locally  or near the  mouth  of  the James River  through cleanup of
Bailey Bay.  Only two cases of cleanup involving 32 to 56 kilometers (20 to 35
miles) of  river  reach  in the turbidity maximum zone showed significant local-
ized improvement.  None of  the cleanup  options has any  appreciable  effect on
the  contamination near the mouth of  the James River.  In addition, none of the
partial   cleanup  options  reduced  the levels  of  contamination  sufficiently to
eliminate  the hazard  of  bioaccumulation  of Kepone  by  fish  to the action lev-
els.  It was therefore concluded  that "hot spot" or partial  cleanup operations
could  not be  recommended.   However,  partial  cleanup  of  "hot  spots"  would
potentially  reduce  the time  for  closure   of  the river  due  to contamination.
Accordingly it was recommended that the dredge spoil from maintenance dredging
of the river  be removed to safe land  containment sites.

                     NONCONVENTIONAL MITIGATION APPROACHES

     In   addressing  nonconventional   mitigation  methods,  the project  team fo-
cused on  evaluating  alternatives  to  dredging, as  well  as  treatment and/or
fixation processes complementary  to dredging for application to Kepone contam-
inated  sediments  in the  James River System.   Four types of  alternative ap-
proaches  were  studied:   dredge spoil  fixation, elutriate  treatment,  J_n  situ
stabilization,  and isolation.

DREDGE SPOIL FIXATION

     Dredge  spoil  fixation is necessary  to  prevent  leachate  of contaminated
materials  from  the dredged spoil site.  Fixation  processes  investigated  were
classified according to  base  ingredients.   These included:   silicates, organ-
ics,  sulfur,  gypsum,  and  asphalt.   Twenty-one samples  were tested  and the
sampling  included  eight  different companies.   A silicate-based, organic-based
and  sulfur-based  fixation  agent  showed  the most promise for the Kepone appli-
cation.
                                     252

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Silicate-Based Agent

     In general, most  silicate-based  agents  rely on high pH conditions to set
the stabilized material.  Kepone  is  solubilized under these conditions and if
the fixation additive  does  not isolate the Kepone,  it  will  occur in leachate
at  equivalent  or  higher levels  than is  found with natural  sediments.   The
Japanese  firm  Takenaka  utilizes  a  silicate-based  agent.   However,  they im-
proved their additive agents over the first series of tests which indicated no
better  fixation  capabilities than  natural  sediments.  Results  of  the latest
fixation efforts on Bailey Bay sediment samples showed leachate Kepone concen-
trations of only  0.08  ug/1  (ppb) in fixed sediments which originally showed a
leachate of  .57 ug/1  (ppb)  of Kepone.  Takenaka officials  believe  that they
can reach a  level of 0.01 ug/1  (ppb) to 0.03 ug/1 (ppb).

     The  Takenaka  technology  offers  the  advantage  over other  fixation pro-
cesses  in that fixation can be performed in-place.  Most processes necessitate
removal,  treatment  and then  replacement of the  fixed  material,  thus adding
considerably to the  costs  of the process.  In addition, the Takenaka technol-
ogy has  had widespread operational  use  in Japan  under  a range of conditions.
Large  scale projects  have   been  ongoing  for   several  years  in  contaminated
harbors and rivers  in  Japan, and involve  fixation  of contaminated industrial
sludge, contaminated dredge spoil, and i_n situ fixation operations on contami-
nated  bottom  sediments  at   depths  up  to  40  meters.   To date,  the  fixation
processes have  been  used effectively on sludge  contaminated  by mercury, cop-
per, zinc, cadmium,  lead, chromium, and  PCBs.  Laboratory tests have shown the
processes to be  effective on arsenic as well.

Organic-Based Agent

     Por  Rok  Epoxy  Sealant,  an  organic base  fixation  agent,  is a synthetic
epoxy material  which is mixed with a coarse aggregate material and is used as
a  grout or  surface sealant.   It  reduced Kepone  leachate  concentrations an
order of magnitude lower than those of standard  sediments.  This stabilization
agent  showed  promise  as a  means  of reducing  Kepone  releases  from spoils.
However, application costs are high - $442/m3 ($12.50/ft3) and the material is
limited in availability.

Sulfur-Based Agent

     Molten  sulfur  used  as a  fixation  agent  offered  an order  of magnitude
reduction of  leachate  concentrations  in laboratory  tests.  However, the  prac-
ticality of molten sulfur for a large scale application to Kepone contaminants
is  unknown.  Furthermore, it  is  recognized that there could be severe eviron-
mental  impacts  associated  with  this  dredged  spoil  fixation  process because
elemental sulfur, while stable in water, readily changes to soluble and poten-
tially  toxic  forms  when  mixed with reducing  as  well  as  oxidizing sediments.
Molecular compounds  of concern include carbon disulfide, hydrogen sulfide and
sulfur  dioxide.   These  compounds  should be handled carefully.  Accordingly,
the molten  sulfur  technique will  require additional  investigation and evalua-
tion.
                                      253

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ELUTRIATE TREATMENT

     The elutriate associated with contaminated dredged spoil  material  must be
treated prior to return of the elutriate to the receiving waters.  This treat-
ment is especially critical with Kepone-contaminated elutriate since Kepone in
low concentrations  can be bioaccumulated rapidly.

     Elutriate/slurry treatment methods investigated consisted of:  photochem-
ical degradation;  amine photosensitization;  chlorine  dioxide,  ozone  and UV/
ozone treatment  in  combination  radiation  with gamma rays and  electron beams;
catalytic reduction; and carbon adsorption.

     Based on the study investigations, the UV/ozone and the temporary filtra-
tion/carbon adsorption  scheme were deemed best suited for elutriate treatment.

Ultra-Violet/Ozone Treatment

     Research on  combined ozonation and  ultra-violet  irradiation by Westgate
Research Corporation exhibited  better  than 80 percent Kepone removal from the
effluent of  Hopewell's  primary  treatment  plant when samples were subjected to
exposure periods of one  hour.

     Cost  projections  for  large  treatment plants,  developed  by Westgate Re-
search  for other applications  indicate  a capital  cost of  $33,022  to  $37,000
per MLD  ($125,000  to $140,000 per MGD) capacity and operation and maintenance
costs,  including amortization,  of $.03 per 1,000 liters ($0.11 per 1,000 gal-
lons) treated.

     In  continued  research to determine  whether ultraviolet  irradiation pro-
cesses  are  limited  to clear  samples  receiving  direct  irradation,  Westgate
treated  sediment  slurry samples  taken from  a  contaminated creek bed.  There
was  a  significant  loss of Kepone, 63.8  percent,  in  the sediment  during the
first 30 minutes  of reaction time.  It is  believed  that  Kepone is being des-
troyed in  the water phase, and that the partition coefficient permits continu-
ous  release  of  Kepone  from the sediment to the water.  This could explain the
relatively  constant values obtained  in  the  supernatant  analyses.   The sedi-
ment,  about 20  percent  by  volume, was  held  in  suspension   in  the "Ultrox"
reactor by the  ozone spargings  (Westgate,  1978).  This ability to handle high
solid content slurries  also holds promise for the  direct treatment of dredged
slurries or  sediments,  if the sediments are  put in slurries  of 20 to 50 per-
cent solids.  However,   further evaluation of the process is  required to deter-
mine the extent of Kepone degradation and assess the potential toxicity of the
by-products.  It  appears  that  degradation  occurs  by  the removal  of chlorine
from the Kepone  molecule forming monohydroKepone.

     From  these very preliminary but encouraging results,  it is estimated that
an  optimum large-scale  portable treatment system could treat 20 to 50 percent
solids  slurry  for  13  to  26 cents  per cubic  meter (10 to  20  cents  per cubic
yard),  not  including   equipment  amortization.   However,  further testing  is
needed to adequately define operating parameters and associated costs.
                                     254

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     No major  environmental  impacts  are  anticipated with  the  application of
the UV/ozone  treatment process other than those  associated with construction
of the  facilities  and  the increased demand for power.  However, as indicated,
by-products and/or deleterious  residues have not been studied.

Filtration/Carbon Adsorption

     During the  decontamination efforts  in  early  1976, the  EPA mobile spill
treatment  unit  was brought  to Hopewell  to help  decontaminate  washwaters  and
liquid  wastes.   Carbon  adsorption  proved effective  in removing  Kepone  from
solution.   Accordingly,  the  Kepone project  team contacted  companies  experi-
enced in large scale applications of carbon adsorption  treatment.

     The  Calgon  Corporation  has   developed   a   filtration/carbon  adsorption
wastewater  treatment   system  which shows  promise  in treating  dredge  slurry
water containing Kepone.  In their conceptual  design, the dredged slurry would
be  pumped from  the  dredge  to  an  impoundment  basin  where the  solids would
settle  from the  water.   From the impoundment basin the  water  would flow to a
gravity slow  sand  filter, constructed in a lined  earthen basin.  From the sand
filter  the water  would flow by gravity to an adsorption basin and be directed
through a bed containing a layer of gravel and a  layer of Filtrasorb activated
carbon.    From  the filter bed,  operated   in  a  flooded  condition  to  prevent
channeling, the  treated  water  would overflow to a spillway and be returned to
the river.  At the conclusion  of the dredging, the entire sand filtration and
carbon  beds  could be  encapsulated  and backfilled  to  prevent  future leachate
contamination.  Calgon estimates the  capital  costs for a 50  MLD unit  at $.81
million (50 MGD  unit  at $3.06 million).   More extensive  analysis  of the site
and operational  requirements  will be required to develop operating costs.

Comparison of the Ultra-Violet Light/Ozone and Filtration/Carbon Adsorption

     Both the UV/ozone treatment system,  proposed by Westgate Research Corpor-
ation,  and the  temporary filtration/carbon  adsorption wastewater treatment
system  proposed  by Calgon Corporation were recommended for further evaluation
for elutriate treatment.  The UV/ozone option seems to destroy Kepone,  but the
degradation products and their relative  toxicity still need to be determined.
The use of the  temporary filtration/carbon adsorption  option  may still  pose
disposal problems if future leachate contamination is to be prevented.

IN SITU STABILIZATION AND ISOLATION

     If} situ  stabilization  processes  as  a category are  the newest of the ap-
proaches  to removal/mitigation of in-place toxic  materials.   As such, most are
less  developed  than  other  approaches.   Several  of  the  more  promising  new
options were  selected  for testing  in the Battelle  laboratory.  Since biologi-
cal approaches currently evaluated  appear to offer little with respect to the
removal of Kepone from the James River system, work focused on two types of j_n
situ  approaches:   use  of sorbents  and  use of polymer  films.   In  addition to
these approaches,  the  Japanese Takenaka  fixation process previously described
can be  used  in  j_n situ  mitigation  of  contaminants.  (The  Japanese fixation
process  is a  proven   large  scale  operational  in-place  fixation  technology.
This fixation process  generally costs $13 to $20 a cubic meter, and eliminates
                                      255

-------
removal costs).  However, indications  are  that the top few centimeters at the
sediment/water  interface may  be  difficult  to  fix.   Consequently,   such  an
application  for  Kepone,  with  the  present  state  of  knowledge,  is  far  less
desirable than removal of the contaminated sediments and fixation in carefully
contained  dredge  spoil  sites.   Also  any in-place  fixation  technique  may  have
major impacts on benthic communities.

     Natural sorbents (such  as  activated carbon) and synthetic sorbents (such
as the macroreticular resins) have been shown to  be effective in concentrating
organics  similar  to  Kepone.   In  application,  sorbents  act much  as  natural
sediments  do  in maintaining  levels of Kepone  much  higher  than those in adja-
cent waters.  Sorbents  having  lower  partition values (concentration in water/
concentration  in  substrate) than  those exhibited  in natural  sediments  will
reduce the  levels of  dissolved Kepone in the  water if introduced to the sys-
tem.  A three-phase  equilibrium is established with the highest concentrations
of  Kepone  on  the  new  material, a lower concentration on the sediment, and the
lowest concentration in  the water.

     Based  on Battelle's  initial  screening  results  sorbents ES863,  XAD-4,
XAQ-2, and Filtrasorb 300 were selected for  further study.   The three proprie-
tary  products  are  macroreticular  synthetic  sorbents  produced commercially.
Filtrasorb  300  is  a  commercial  activated   carbon.   In  addition  to  these,  a
specialty carbon product formed around iron particles became available in time
for  subsequent  evaluation.   Allied Chemical  also  performed  laboratory tests
utilizing anthracite coal.

     Following Allied Chemical  Company's  promising initial results with coal,
batch  adsorption tests  were  initiated in the Battelle laboratory on a variety
of  coals.   Results  indicate that  coals  tested  had less  affinity  for Kepone
than Bailey  Bay sediments.   Consequently,  these  coals did not offer any miti-
gation  utility  for  Bailey  Bay sediments.    However,  Bailey  Bay sediments are
high in  organic content and testing on more representative James River sedi-
ments  should  be undertaken  before  final  determinations are made on the appli-
cabi1ity of coal.

     Although  sorbents  applied to sediments j_n  situ  are  capable of reducing
the  availability  of  a  material  to the  water column, they  do  not destroy or
remove the  contaminant.   Removal  can  be  achieved,   however,  if  media  are  made
to  be  retrievable.  Laboratory  work  at Battelle  indicates that this is possi-
ble  through the inclusion of magnetite or iron particles in the sorbent matrix
which  will  render  the  media particles  susceptible  to magnetic fields.  How-
ever,  the practical application is unevaluated.    The  magnetic sorbents would
have to  be mixed into the river sediments and  then  recovered.  Strong magnetic
fields  may  be  required  and  dispersion  of contaminants  avoided.   Costs for
using  synthetic sorbents are prohibitively expensive on wide scale application
unless  they can  be  made  retrievable.  Even  then,  costs  of  using synthetic
sorbents  is  estimated  to  be $31/m3,  (0.90/ft3) sediment  compared to $l.l/m3
($0.032/ft3)  sediment for coal and $18/m3  ($0.52/ft3)  sediment for activated
carbon.

     It  was  noted  previously  that  activated  carbon  had  been  successfully
applied  to  remove  Kepone  from  solution.    The  same is true  for any  of the
                                     256

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sorbents  found to  be effective  for  i_n  situ evaluations  such as  XAO-2 and
ES863.    Consequently,  sorbents,  if  developed  for  operational  application,
should be considered as candidates for both elutriate and j_n situ application.
In j_n situ  use,  activated carbon might be considered for application directly
to the  river  without  retrieval.   This would be  done  in the same manner as an
application of coal,  but  activated  carbon offers a high degree of adsorption.
However,  availability  of  the  resultant  contaminated carbon to  the  biota has
not been evaluated.

     Of the J_n  situ approaches considered, all show some degree of effective-
ness.   The potential of using coal is still not  resolved.  Based on laboratory
comparisons,  activated carbon  is more appropriate than coal  as  an  i_n situ
additive.  Any J_n  situ use  of activated  carbon or coal,  if  it proves to be
operationally effective,  would be limited in application to areas contaminated
to less  than  1  pl/g (ppm).   In areas where Kepone concentrations were greater
than or equal to 1  ug/g (ppm), retrievable media or fixation techniques should
be given  further consideration.   The  latter exception  is made  to  reflect the
fact that  at  high  Kepone  concentrations in sediments, the potential  reduction
in Kepone  availability with  coal  or  activated carbon  would still  allow unac-
ceptable  levels  of Kepone  in the water.   For these  areas,  retrievable media
and fixation,  if effective, would be costly.

     Environmental   impacts  associated  with j_n  situ  treatment  are  not well
understood.   However,  j_n  situ  treatments  potentially  pose  many  physical,
biological and chemical  impacts  on  the river  and  its biota.   Accordingly, no
j_n situ  treatment approaches are recommended at this  time  for the James River.


           NATURAL DEGRADATION AND BIOLOGICAL MITIGATION APPROACHES

     As part of the Kepone Mitigation Feasibility Project, natural  degradation
and biological  approaches  seemed viable avenues for  amelioration  or elimina-
tion  of  the  Kepone contamination  problem.   They  were  examined concurrently
with engineering approaches.   These  methods,  if  they proved successful, could
offer the possiblity  of  in-place mitigation  without  elaborate or  expensive
engineering programs or structures.   Our investigation of potential biological
mitigation  methods included:   (1)  degradation  or destruction  of  Kepone by
microorganisms; and  (2)  biological  uptake and  concentration  of Kepone by an
animal  or  plant with  subsequent harvest and destruction.  Natural  biodegrada-
tion of  Kepone was the most hopeful route because many  substances are capable
of some  degredation by  natural means.

DEGRADATION

     A  search of  the literature indicated  only indirect  and circumstantial
evidence  that Kepone   could  degrade,  either  photochemically  or biologically.
Laboratory efforts were aimed at degradation studies under a variety of condi-
tions,  including aerobic  and anaerobic situations.   The EPA Gulf Breeze Envi-
ronmental  Research  Laboratory  and   Battelle  Pacific  Northwest Laboratories
performed  experiments to  determine  if Kepone degradation would  occur under
laboratory conditions.
                                      257

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     Studies  by  Garnas  et al_.  (3)  and  Bourquin  et al_.  (4)  of  Gulf  Breeze
employed  static  water/sediment  systems   to  assess  both  biological  and  non-
biological  degradation  of  Kepone.   James  River  sediments  with  and without
Kepone were used  and  the fate of Kepone  monitored with  radio-labelled Carbon
14 material  and  with total  budget chemical  analyses.  The  investigators em-
ployed a  variety  of  experimental  conditions including  oxygen  concentration,
nutrient  additions,  Kepone levels,  sediment sources, sunlight,  temperature,
and salinity.

     Gulf  Breeze  experiments  indicated  that Kepone  does not  degrade  either
biologically  or   chemically   in  the  laboratory  situations,  which  simulated
natural states as  closely  as  possible.   These results indicate  that currently
evaluated degradation processes will  not reduce  the levels of Kepone now found
in the water and sediment of the James River.

     The Battelle  Laboratories found  results similar to  those of Gulf Breeze.
While  some  evidence  exists that  certain  bacteria  can  survive  in the presence
of Kepone-contaminated  sediments,  degradation  of  Kepone has not  been demon-
strated or  confirmed.  The half-life of Kepone in the environment has not been
determined, but  laboratory evidence suggests it may be  on the  order of dec-
ades.

     Fungi  offered  a  potential for Kepone degradation, and  Atlantic Research
Corporation believes  they have  a  series  of fungi which  will  degrade Kepone.
One  isolate  showed  41   percent  disappearance  of  Kepone  in 22  to  31  days.
However, these experiments  have  been  performed  only in the laboratory, and no
seal ing-up  has  been attempted.  The  fungi  may  have  difficulty competing and
surviving  under  natural  conditions,  thus their  usefulness  is  restricted  to
controlled  environments, such  as  containment lagoons.  Such an  approach would
not be  feasible for the amounts  of Kepone-contaminated sediments in the James
River which need treatment.

BIOLOGICAL UPTAKE  AND  HARVESTING

     Studies  with  other  chlorinated  hydrocarbons have shown that  they  can  be
bioconcentrated by plants  and that uptake  increases with  water  solubility.
However,  studies  to  date  with Kepone  indicate  that plant  uptake  is  not  an
effective mechanism for mitigating Kepone in the  environment.

     Algae  were  found  to  bioaccumulate  Kepone  to as much  as  800  times the
ambient levels of  Kepone (5).  This  approach was examined for the possibility
that  Kepone-contaminated  algae could  be  harvested and destroyed by incinera-
tion  to  eliminate the  Kepone.   Problems, similar  to those of  fungi,  became
apparent.    Furthermore,  the  algae bioconcentrated Kepone from  the water in-
stead of the sediments where the bulk of the Kepone is located.

     In a  similar fashion, Kepone  attached to  rooted aquatic  plants such  as
water  hyacinths,  could  be isolated,  harvested  and  destroyed.  Although the
water  hyacinths may  accumulate Kepone  on their  leaf  surfaces,  the plants are
free-floating and would  not  be in contact with  the large percentage of Kepone
which  resides in  the  James River sediments, giving  this  method limited value
for mitigation purposes.
                                     258

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     Although Kepone is  intimately  bound to sediments of  the  James River, it
can desorb  from those sediments, or organisms can extract  it  from the sedi-
ments to  become incorporated  into  living systems.  It  can  be  passed between
organisms readily as one animal  uses another  as  food.   Kepone  is also avail-
able to  animals from the water.   Although animals  can  bioconcentrate Kepone,
they were  never  viewed   to  have utility for  Kepone  uptake with  subsequent
harvesting to destroy  the Kepone.   As with plant harvesting the logistics are
impractical.   Ultimately any  mitigation  method  proposed  to   ameliorate  the
effect of  Kepone must address the  bioconcentration of  Kepone  by James River
organisms, which traditionally  have been used as a  food resource.


                  SUMMARY OF RECOMMENDED MITIGATION APPROACHES

     The project findings which  lead to the recommended mitigation approaches
are too  extensive  to detail  here.   These are covered in the Kepone Mitigation
Project Report  (2).  However, some of the key findings  will be summarized here
as  they  relate  to  specific  recommended mitigation  approaches.  A special task
force consisting  of representatives  from EPA and  the States  of  Virginia and
Maryland has  already been established to consider and implement the recommen-
dations.

CHESAPEAKE BAY MITIGATION APPROACHES

     Modeling and  monitoring  studies  indicated  that  Chesapeake  Bay  is not
currently threatened by  the contamination of the James River.  However, severe
storms  and   like  events   could  alter  the situation.   Accordingly, continued
systematic monitoring  of Kepone  levels in water sediment and biota was recom-
mended.   In  addition,  development of a long  range  strategy  including use of
submerged  silt  dams  to   implement  emergency  mitigation measures  was recom-
mended.

JAMES RIVER MITIGATION  APPROACHES

     Based on the  enormous  costs  of total James  River  amelioration efforts,
the lack of  knowledge  on ecological  impacts of widespread mitigation efforts,
the unavailability of  economic impact determinations,  and supportive evidence
that most  of  the  Kepone will remain  in the  zone of  turbidity  maximum,  no
full-scale cleanup  action was  recommended for the James  River at  this time.
However, since  navigational  dredging  is  required  in  the James  River,  these
dredging operations afford a continuing opportunity to initiate removal of the
contaminated  sediments.   Accordingly, it was recommended that the Oozer dredge
be  considered for  such  dredging and the  dredge spoil  be  disposed  of in ade-
quately protected dredge  spoil  sites developed along the James River.

     Among the  key  issues deterring progress  in  physical  removal  of the con-
taminated  sediments  from the  James  River were  uncertainties  regarding the
effectiveness and  costs  associated  with  treatment of  elutriate  and dredge
spoil.   However, promising  technologies were  found whose  further development
was recommended.   Two  of the technologies were  recommended  for developmental
funding—the  Takenaka  fixation  technology developed  for  Kepone-contaminated
sediments and the UV/ozone treatment of Westgate Research.
                                     259

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HOPEWELL AREA MITIGATION APPROACHES

     Contamination of  the  land  around  the Hopewell area  is  extensive.   Some
limited land  areas within  the  city limits, accessible  to the  population, have
levels ranging to  1,530  ugg  (ppm).   Accordingly,  it was recommended  that the
health threat  be assessed—the  most  expeditious  action being  removal  of the
contaminated soil and disposal.

     A marsh area  contiguous  with a  creek discharging  into Bailey  Bay and
thence the James  River  was found to contain an estimated  1,363 kg (3,000 Ib)
of Kepone.   Containment  or physical  removal of the  contaminated  material was
recommended.

     A lagoon  containing Kepone-contaminated  sludge obtained  from  the  early
cleanup operations around  Hopewell  has  suspected  leakage into a nearby creek.
It was recommended that the material  be  removed from the lagoon or covered and
containment be initiated.
                                    CLOSURE

     United States'  experience in handling in-place  toxic  pollutant problems
of  the  extent  exhibited by  the Kepone  contamination in  the  Hopewel1/James
River area is limited.  However, adaptation of Japanese technology in dredging
and sediment fixation holds promise for substantial  assistance in solving such
problems.   In  addition,  it  is  hoped that  the  investigative  techniques  and
findings of the  Kepone  Mitigation Feasibility Project will  not only provide a
basis for moving  forward with  the solution of the  Kepone contamination prob-
lem, but will provide an approach to  solution of  other serious waterway con-
tamination problems in the United States.

                                  REFERENCES

1.   Mackenthun,  K.M. ,  M.W.  Brossman,  J.A.   Kohler,  and  C.R.  Terrell,  1977.
     Mitigation Feasibility for the Kepone-Contaminated James River, Virginia.
     Presented at  the Third  Annual  U.S./Japan Meeting on  Management of Bottom
     Sediments,  Easton,  Maryland,  September 1977.

2.   Brossman,  M.W.,  K.M. Mackenthun,  J.A.   Kohler,  and  C.R.  Terrell,  1978.
     Mitigation  Feasibility  for  the  Kepone-Contaminated  Hopewell/James  River
     Areas.   EPA Report, Washington, D.C., June 9, 1978.

3.   Garnas,  R.L.,  A.W.  Bourquin  and P.H. Pritchard,  1978.   The  Fate  of 14-C
     Kepone  in  Estuarine Microcosms.  Presented at  175th National  Meeting of
     the American Chemical Society, Anaheim, California, March 1978.

4.   Bourquin,  A.W.,   P.H.   Pritchard  and  W.R.  Mahaffey,  1977.   Effects  of
     Kepone  on  Estuarine  Microorganisms.   Developments in  Industrial  Micro-
     biology, Vol.  19  (in press).

5.   Walsh,  G.E.,  K.  Ainsworth  and A.J.  Wilson,   Jr.,  1977.    Toxicity  and
     Uptake of  Kepone  in Marine Unicellular Algae.  Chesapeake Science 18(2):
     222-223.


                                     260

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           PCB CONTAMINATION OF THE SHEBOYGAN RIVER,  INDIANA HARBOR
                           AND SAGINAW RIVER AND BAY

                               Karl E.  Bremer
                     U.S.  Environmental  Protection Agency
                            Chicago, Illinois 60604
                                   ABSTRACT

     Current  PCB  contamination in  three  harbor areas of the Great  Lakes  has
resulted in problems  related  to maintenance dredging, disposal,  or  fish con-
tamination.   The  Sheboygan  River  shows  high PCB residues in fish  and bottom
sediments as  a result  of  improper PCB disposal.  Indiana Harbor, one of  the
most highly contaminated harbors  in the Great Lakes is experiencing delays in
maintenance dredging  of  approximately  750,000 cubic yards of bottom sediment.
High concentrations of  mercury,  lead,  zinc, manganese, arsenic, and PCBs have
been detected  throughout the  harbor and ship canal.  A new dike disposal area
has been  completed in  Saginaw Bay.  Possible  use  of this  confined disposal
site will  be made for PCB-contaminated sediments  from the Saginaw River.
                                 INTRODUCTION

     There are approximately  180  harbor areas in the  Great  Lakes  Basin which
are served by  commercial  shipping.   To maintain a minimum depth of 8.2 meters
(27 feet) in  these  harbors,  continued maintenance dredging  occurs  at various
harbor areas  along the extensive shoreline of the Great  Lakes.

     The  United  States  and  Canada  continue to maintain  these ports  with  a
joint determination to restore and enhance water quality.  In the Agreement on
Great Lakes  Water  Quality of  April   15,  1972,  the Governments  of  the United
States and Canada directed  that  specific attention be given to assessing the
potential  for  deleterious  environmental   aspects  from  dredging  activities
within the Great Lakes  basin.   In addition, two Acts  have been passed within
the last  three years  to  specifically deal  with toxic substances  problems in
both  countries.   In Canada,  the  Environmental  Contaminants  Act,  and  in the
United States, the  Toxic  Substances  Control Act have  been implemented.  These
Acts will definitely  impact  dredging activities on the Great Lakes during the
next few years.

     As part  of  the U.S.  role in maintaining Great Lakes water quality, toxic
contaminant problems  were evaluated  in three waterways  of  particular impor-
tance:  the Sheboygan River, Indiana Harbor,  and Saginaw River and Bay.
                                     251

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                                SHEBOYGAN RIVER

     The Sheboygan River  and  its  tributaries,  the Mullet  River,  Onion River,
Weedens  Creek,  and  Greendale Creek  flow  east  to the  western  side  of  Lake
Michigan in  the  State  of Wisconsin.   The River enters Lake Michigan through a
450-foot-wide outer basin  of Sheboygan Harbor.

     During 1975, 1976 and 1977,  the Wisconsin  Department of Natural Resources
(the State pollution  control  agency in Wisconsin) analyzed  Lake  Michigan and
Sheboygan  Harbor  fish for PCB contamination (1).  Average  PCB  concentrations
in  Sheboygan  Harbor  fish  were  similar  to  PCB levels found  in  Lake Michigan
fish  along  the  coast  (Table 1).   Average PCB  concentrations   in  Sheboygan
Harbor  sediments  in  1977, as analyzed  by  the U.S.   Environmental  Protection
Agency  (Table 2)  were  also low when compared with other Lake Michigan harbors
(2).

     In  March 1978,   the  Wisconsin  Department  of Natural  Resources analyzed
fish from  the Sheboygan River at a location three miles upstream from Sheboy-
gan Harbor.  Test results for whole fish ranged from 26 to 750 ug/g (Table 3).
To  confirm these analyses,  additional  samples were  obtained March 31,  1978.
These  results ranged  from 8.3 to 241.5  ug/g.  PCB concentrations in all  fish
exceeded the  U.S.  Food and Drug Administration's temporary tolerance level of
5 ug/g.

     In April 1978,  the Wisconsin Department of Natural  Resources and Depart-
ment of  Health and Social Services advised the  residents  of Wisconsin not to
eat fish from the Sheboygan,  Mullet and Onion Rivers.  During the same period
of  time, an  investigation was conducted to test  fish,  river sediments,  muni-
cipal  and  industrial  effluents,  and river water in the Sheboygan River drain-
age basin.

     Fish  were  collected  for  PCB analysis at  11  locations  in  the Sheboygan
River  drainage  basin  (Figure  1).   PCB concentrations in  fish taken from the
Sheboygan  River lakeward  from Sheboygan Falls Dam to Lake Michigan ranged from
0.9  to 970.0 ug/g (Table 4).  The  mean concentration  for  these samples was
155.0  ug/g.  Thirty-eight fish  samples  upstream of Sheboygan Falls Dam on the
Sheboygan,  Mullet and Onion Rivers contained PCB concentrations  below the U.S.
Food and Drug Administration's temporary tolerance level  of  5 ug/g.

     Bottom  sediments  were analyzed  at 13 locations  in the Sheboygan  River
drainage basin.    Concentrations in  sediments  ranged  from 0.1 to  190 ug/g PCB
(Table  5).   The  highest PCB  concentrations were detected in sediments immedi-
ately  downstream from  the Tecumseh  Products  Diecasting  Plant  in Sheboygan
Falls.   PCB  concentrations showed  a  decline  at  locations further downstream
from the diecasting facility.

     The Wisconsin Department of  Natural Resources analyzed PCBs in municipal
and  industrial   effluents collected  from  facilities in  the drainage  basin
(Table  6).   In  addition,  PCBs were analyzed  in river water  and in hydraulic
fluid  taken   from  three  aluminum  die-casting  plants.   Significant  PCB  point
sources to the Sheboygan  River were not detected by monitoring these municipal
and industrial discharges.


                                      262

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         TABLE 2.   BULK SEDIMENT CHEMISTRY PCB AND PESTICIDES ANALYSIS
                             (All values are mg/kg dry weight)

HARBOR:    Sheboygan small  boat harbor, Wisconsin
SAMPLED:   September 16, 1977

Sample Site
Compound
Hexachlorobenzene
beta Benzenehexachloride
Li ndane
Tref Ian
Aldrin
Isodrin
Heptachlor Epoxide
gamma Chlordane
o,p -DDE
p,p'-DDE
o,p -ODD
o,p -DDT
p,p'-DDD
p,p'-DDT
Methoxychl or
Mi rex
2,4-D, Isopropyl Ester
Endosulfan I
Dieldri n
Endrin
Endosulfan II
DCPA
Tetradifon
Aroclor 1016 (1242)
Aroclor 1248
Aroclor 1254
Aroclor 1260
Total PCB
SHB77-1
*
*
*
*
<0.02
<0.02
*
<0.02
*
<0.02
*
<0.03
<0.02
<0.04
*
*
*
*
*
*
*
*
*
0.149
*
• 0.167
*
0.316
SHB77-2
*
*
*
*
<0.02
<0.02
*
<0.02
*
<0.02
*
<0.03
<0.02
<0.04
*
*
*
A
*
*
*
*
*
0.047
*
0.044
*
0.091
SHB77-3
*
*
*
*
<0.02
<0.02
*
<0.02
*
<0.02
*
<0.03
<0.02
<0.04
*
A
*
*
A
*
A
*
*
0.028
*
0.027
*
0.055
SHB77-3
Repl icate
*
*
*
*
<0.02
<0.02
*
<0.02
*
<0.02
*
<0.03
<0.02
<0.04
)*C
>ปc
>*;
*
*
X
*
*
*
0.040
*
0.055
*
0.095
SHB77-4
*
*
*
A
<0.02
<0.02
*
<0.02
*
<0.02
*
<0.03
<0.02
<0.04
*
A
*
A
A
*
*
*
*
0.070
*
0.035
*
0. 105

 ^Concentration less than 0.01 mg/kg.
                                     264

-------
TABLE 3.   PCB CONCENTRATIONS OF WHOLE FISH OBTAINED FROM THE SHEBOYGAN RIVER
          THREE MILES UPSTREAM FROM SHEBOYGAN HARBOR

Sampl i
ing Date
September
September
September
March 31 ,
March 31 ,
March 31 ,
March 31 ,
March
March
March
March
March
March
31,
31,
31,
31,
31,
31,
9, 1977
9, 1977
9, 1977
1978
1978
1978
1978
1978
1978
1978
1978
1978
1978
Species &
Length
5 Carp (12-23 inches)
5 Northern Pike (18-25 inches)
5 White Sucker (10-14.5 inches)
17 Black Bullheads (3.5-9 inches)
12 Black Bullheads (4-9 inches)
1 Rock Bass (8 inches)
2 Common Shiners (4 inches)
1
2
3
4
5
4
Coho
Salmon
Walleye (
Carp
Carp
(10-
17
18
(23-24
Suckers (
Northern
PCB Concentration
(jg/g (ppm)*
750
55
26
41.
34.
10.
49.
(23 inches) 8.
i
.5
i
nches)
inches)
nches)
12-21 inches)
Pi
ke
(21-27 inches)
241.
180.
158.
30.
62.
8
3
0
8
3
5
0
4
0
.6

*ppm - parts per million
                                     265

-------
I	SJ._ANN_A
                                           -4-HWYA

                                       ONION OOSTB
                                       RIVER
                                                                          COAST GUARD
                                                                               STATION

                                                                         KI WAN IS PARK

                                                               ioHLEpDAlISHEBOYGAN

                                                                   FALLS\DAM
                                                               WEEDEN'S X  LAKE MICHIGAN
                                                               CREEK
                                                                 FROM U.S.6.S. I:500,OOOBASI
     Figure 1.  Sheboygan  River drainage basin (PCB  investigation area)
                                         266

-------

Sampl ing
Date
Kiwani s
5/16/78
5/16/78
5/16/78
5/16/78
5/16/78
5/16/78
5/16/78
Greendal
4/28/78

4/28/78
4/28/78
4/28/78

4/28/78
4/28/78
Species and
Average Length
Park Samples
1 Carp (27 in. )*
1 Carp (23 in.)*
"1 Carp (22 in.)*
"! Carp (25 in. )
1 Carp (23.5 in. )
1 Carp (24.5 in.)
4 Suckers (14 in.
e & Weeden's Creek Sampl
1 Northern Pike
(15.0 in. )**
8 Minnows (6.0 in
17 Minnows (4.5 in
1 Coho Salmon
(14.5 in.)**
6 Creek Chubs (6
18 Mi nnows (5.0 in
Sampling PCB Concentration
Location M9/9 (ppm)***

Kiwanis Park-Sheboygan
Kiwani s Park-Sheboygan
Kiwanis Park-Sheboygan
Kiwanis Park-Sheboygan
* Kiwanis Park-Sheboygan
* Kiwanis Park-Sheboygan
)** Kiwanis Park-Sheboygan
es
Greendale Creek

. )** Greendale Creek
. )** Greendale Creek
Weeden's Creek

in.)** Weeden's Creek
. )** Weeden's Creek

15.3
17.0
12.1
2.0
333.0
970.0
23.9

169

5.9
14.0
0.9

150.0
61.0
Kohler Dam Samples
4/26/78
4/26/78
4/26/78
4/26/78
4/26/78
4/26/78
4/26/78
4/26/78
4/26/78
4/26/78
4/26/78
4/26/78
4/26/78

4/26/78

1 Carp (25 ;n. )*
1 Carp (25 MI. )*
1 Carp (?2 in. )*
1 Carp (25 in. )*
3 Carp (22-25 in.
1 Carp (27 in.)*
5 Carp (18.5-20 i
3 Carp (21.5-22 i
5 Suckers (12.5-1
5 Suckers (9-10. 5
5 Suckers (10.5-1
5 Suckers (10-11
5 Rock Bass
(4.5-7.5 in.
12 Common Shiners
(5 in. )**
Above Kohler DanrKohler
Above Kohler DanrKohler
Above Kohler DanrKohler
Above Kohler Dam-Kohler
)** Above Kohler Dam-Kohler
Above Kohler Dam-Kohler
n. )** Above Kohler Dam-Kohler
n. )** Above Kohler Dam-Kohler
3 in.)* Above Kohler Dam-Kohler
in.)** Above Kohler Dam-Kohler
1 in.)**Above Kohler Dam-Kohler
in.)* Above Kohler Dam-Kohler
Above Kohler Dam-Kohler
\**
Above Kohler Dam-Kohler

240.0
180.0
150.0
250.0
350.0
250.0
460.0
320.0
88.0
130.0
39.0
40.0
190.0

100.0

(continued)
*Indicates bone
**Inaicates who
***
ess fi11et sample
e fish  sample
   ppm - parts per million
                                     267

-------
TABhE 4.   (Continued)
Sampl ing
Date
Species and
Average Length
Sampling PCB Concentration
Location ug/g (ppm)***
Sheboygan Lagoon Samples (above Sheboygan Falls)
4/27/78
4/27/78
4/27/78
4/27/78
4/27/78

4/27/78
4/27/78
4/27/78
4/27/78
4/27/78
4/27/78
4/27/78
4/27/78
Johnsonvi 1 le
4/28/78
4/28/78
4/28/78
4/28/78
4/28/78
4/28/78
4/28/78
4/28/78

4/28/78
4/28/78
Mullet River
5/4/78
5/4/78
5/4/78
5/4/78
5/4/78
5/4/78
Onion River
4/28/78
4/28/78
4/28/78
4/28/78

4/28/78
4/28/78
4/28/78
38 Bluegill (3.5 in.)**
10 Redhorse (8.0 in.)**
2 Crappies (6.5 in.)**
6 Rock Bass (8.0 in.)**
4 Northern Pike
(16.0 in.)*
7 Redhorse (15.0 in. )*
1 Carp (25.5 in.)*
1 Carp (23.5 in.)*
4 Carp (17.0 in.)*
5 Carp (17.0 in.)**
5 Carp (16.0 in.)**
8 Carp (15.0 in.)**
8 Carp (14.0 in.)**
Dam Samples
4 Carp (20 in.)**
4 Carp (17 in.)**
1 Carp (21.5 in. )*
1 Carp (23.5 in.)*
14 Suckers (10.0 in.)**
9 Rock Bass
3 Crappies (6 in. )**
] Large Mouth Bass
(9.5 in.)**
14 Stonecats (5.0 in. )**
60 Minnows (3.0 in.)**
Samples
5 Carp (13.0 in. )**
5 Carp (12.5 in. )**
1 Sucker (10.5 in. )**
10 Suckers (7.5 in.)**
14 Bullheads (6.5 in.)**
9 Creek Chubs (5 in. )**
Samples
5 Rock Bass (6.5 in. )**
3 Carp (13.0 in.)**
5 Carp (15.0 in.)**
1 Northern Pike
(20.5 in.)*
5 Carp (13.0 in.)**
5 Carp (18.0 in.)**
3 Carp (24.0 in )**
Sheboygan Lagoon
Sheboygan Lagoon
Sheboygan Lagoon
Sheboygan Lagoon
Sheboygan Lagoon

Sheboygan Lagoon
Sheboygan Lagoon
Sheboygan Lagoon
Sheboygan Lagoon
Sheboygan Lagoon
Sheboygan Lagoon
Sheboygan Lagoon
Sheboygan Lagoon

Above Johsonville Dam
Above Johnsonvi lie Dam
Above Johnsonvi lie Dam
Above Johnsonville Dam
Above Johnsonvi lie Dam
Above Johnsonvi lie Dam
Above Johnsonville Dam
Above Johnsonville Dam

Above Johnsonville Dam
Above Johnsonville Dam

Mullet River Samples
Mul let River Samples
Mullet River Samples
Mullet River Samples
Mullet River Samples
Mullet River Samples

At Highway V
At Highway A
At Highway A
Below Waldo

Below Waldo
Below Waldo
Below Waldo
5.0
.5
2.0
2.0
1.0

1.0
1.0
—
1.0
3.0
4.0
2.0
2.0

.8
.8
.4
.6
.2
.5
.7
.4

.4
.4

.2
.2
.2
1.0
3.0
.2
„
.2
.4
.2
.2

.2
.2
.2

* Indicates
**Indicates
***
boneless fillet sample
whole fish sample
   ppm - parts per million
                                     268

-------




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     High  PCB  concentrations  were  found  in  soil  samples  collected on  the
Tecumseh property in Sheboygan Falls (Table 7).  Granular oil absorbent mater-
ial deposited  on the property contained  up to 120,000 ug/g  (ppm)  PCB (12%).
This  PBC-contaminated  waste  desposited  on the  dike  bordering  the  Sheboygan
River  is  a significant  source  of PCBs to  the  lower  Sheboygan River.  During
periods  of high  water   the  Sheboygan  River  flows  along the  dike  and  is  in
direct contact with  highly  contaminated  fill  materials.  During rains PCBs in
the dike are  subject to washing  into  the  stream.   PCBs  at  other locations on
the plant  property   are  likely  to soak  into  the ground  and  reach  the  river
through groundwater  discharge.  The area  is subject  to periodic flooding which
occurred as recently  as May, 1978.

     Following the discovery  of  highly contaminated PCB waste deposits at the
Tecumseh Products site,  the Department of Natural  Resources  issued an order on
May 12, 1978 banning further disposal  of solid waste on Tecumseh property.  On
June 21, 1978  the Department issued a second  order requiring the excavation,
collection and proper storage of all  materials likely to contain PCBs from the
dike on the  Sheboygan  River behind the Tecumseh Plant.  PCB-containing mater-
ials  include  oil-absorbent material,  scrap  pressure  hose,   and  oil-soaked
debris.

     On June  21, 1978  the  Department  together with the  Department  of Health
and Social  Services  lifted the warning against fish  consumption in the follow-
ing sections of  the  river basin:   the Sheboygan River from the Sheboygan Marsh
to  the Sheboygan Falls  Dam,  the Mullet  River from Plymouth  to the junction
with the Sheboygan  River at Sheboygan Falls and the Onion River from Waldo to
Gibbsvi1le.

     The PCB warning is currently in effect on the Onion River from Gibbsville
to Sheboygan Falls,  on the Sheboygan River from the  Sheboygan Falls Dam to the
Coast  Guard  Station  at  Lake Michigan and on two tributaries of the Sheboygan,
Weeden's  Creek  and  Greendale Creek.   The  Onion   River,  Weeden's   Creek  and
Greendale  Creek  were included because they are accessible  to migrating main
channel fish.

     At this  time Tecumseh  Products  Company is proceeding with disposal  oper-
ations.  Contaminated wastes  from the dike are being placed  in sealed  drums
and stored according to  State  and Federal regulations until  a suitable dis-
posal  site  becomes available.

                                INDIANA HARBOR

     Indiana  Harbor  is   located  at  the southern  end  of  Lake  Michigan in the
State  of Indiana  near the Indiana - Illinois border.  The harbor consists of a
breakwater  in  Lake  Michigan 1120 feet long, an entrance channel, an anchorage
and maneuver  basin,  and a ship canal  joining  the harbor with the Lake George
Branch and  the Calumet River Branch of the Grand Calumet River (Figure 2).

     During  1977 the  Chicago District  of the U.S.  Army Corps  of  Engineers
proposed  continued  maintenance   dredging   of  Indiana  Harbor  and  respective
navigation  channels  over a  five- to  six-year  period.   It  was  proposed that
                                     273

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                   TABLE  7.   TECUMSEH  PRODUCTS  SOIL  SAMPLES*

Location
S- 18
S-19
S-20
S-21
S-22
S-23
S-24
S-25
S-26
S-27
Sample
Description
8' from east fence, dark oily
spot on ground. Pic. 1
5' from south fence, granular
oil absorbent material, alum.
bits. Pic. 2
10' from bldg. , sandy soil
oil dump area oily soil
Pic. 3
10' from bldg., sandy gravelly
soil, oil dump area oily
sample. Pic. 4
3' from bldg., between oil
sep. & bldg., black tarry
soil sample, oil dump area.
Pic. 5
3' from south fence, low area
below rubble pile, topsoil
sample. Pic. 6
Granular oil absorbent
material, alum, bits, outside
of south fence on dike. Pic. 7
Granular oil absorbent
material, alum, bits, 2'
outside of south fence. Pic. 8
Granular oil absorbent
material & alum, bits on
river side of dike. Pic. 9
Granular oil absorbent
material & alum bits, hydraulic
hose on river side of dike. Pic
Sample
Depth
topsoil -
surface to
2" deep
6" deep
surface to
3" deep
surface to
3" deep
surface to
3" deep
topsoil -
surface to
4" deep
4-8" deep
4-8" deep
4-8" deep
4-8" deep
10
Col lection
Date
Col lector
5-11-78
Sheffy
5-11-78
Sheffy
5-11-78
Sheffy
5-11-78
Sheffy
5-11-78
Sheffy
5-11-78
Sheffy
5-11-78
Sheffy
5-11-78
Sheffy
5-11-78
Sheffy
5-11-78
Sheffy
PCB
M9/9
(ppm)
390.0
120,000.0
2,300.0
660.0
880.0
1 ,500.0
120,000.0
78,500.0
54,000.0
43,800.0

^Laboratory analysis for these samples  was  performed by soaking .5-20 grams of
 sample in acetone for 1-8 hours.   The  extract was  then injected directly into
 the gas chromatograph.   This procedure is  a more rapid procedure for detecting
 high levels of PCB than the standard column elution method.

                                     274

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750,000 cubic yards  of  maintenance dredging from the Harbor will  be placed in
the  Inland  Steel  disposal  area  during  the  next  six  years  (3).   Proposed
dredging will be accomplished using a clamshell.  The excavated materials will
be placed  in barges  and  towed  to  a  rehandling  area  located  outside  of the
inland disposal  facility.   The  excavated  materials will  be  mechanically re-
moved  from  the  barges  using  a  clamshell  on top of the  containment  wall  and
placed in a barge located within the disposal facility.  The dredged materials
will  then  be  bottom-dumped  in the northeast portion of  the disposal  facility
as designated by  the Steel  Company.   A temporary  opening  will  be made in the
existing slag  dike   to  provide  an access  for  the  towboat  and  barge(s) which
will  operate within  the disposal facility.  The opening will be closed immedi-
ately  after  the equipment  has  entered the  disposal area.   The  dike  will  be
reopened to  permit  the equipment  to  leave the  disposal  area once  dredging
operations  have been completed.   This  process  will be  repeated for subsequent
dredging operations.

     In 1977  at  the  request of the Corps of Engineers, the U.S. Environmental
Protection  Agency evaluated sediment  samples in the areas  proposed for main-
tenance dredging of Indiana Harbor.

     Sediment samples were collected by the Surveillance and Research Staff of
the Great  Lakes  National  Program Office,  U.S.  Environmental Protection Agency
at 13  locations  (Figure 2).   Analyses  were performed by  the  Central  Regional
Laboratory   of  the   USEPA,  Region  V.   Macroinvertebrate   identification  and
enumeration was  performed by Hiedelberg College, Tiffin, Ohio (4).

     Sediments obtained from the upstream limits of the harbor (Stations 1 and
2) to  the  easterly   breakwater  (Station  10)  were  black  or  dark  brown silt
containing  visible  oil  and petroleum  odor  (Table  8).   Sediments  lakeward of
Station 10 were  characterized as brown or grey  sand and gravel.   Macroinver-
tebrates   were  identified  at these  locations  during  field  sampling.   Sieve
analysis data confirmed sediments  which were predominantly silt and clay size
at most locations  (Table 9).

     Bulk sediment analysis was performed on all samples (Table 10).  Stations
1 through  11  demonstrated  severe contaminant levels with respect to all para-
meters.  The  lakeward locations  (Stations  12 and 13) showed measurable reduc-
tions  in mercury,  lead, zinc, manganese,  and  arsenic  when compared with mea-
surements taken  at other stations.

     The elutriate tests  show releases  of iron, manganese, and aluminum from
virtually  all  samples  (Table  11).   All  samples  except those obtained from
Stations 12  and  13   showed  release  of TKN,  ammonia,  cyanide,  and  phenols.
Arsenic  was   released  from samples  at  locations   3,  5  (replicate),  and 11.
Mercury was  released from  samples at Stations  1  through  5,  8, 12  and  13.  In
general, samples  from  locations  1  through  3  exhibited  the  most  release and
samples from locations 12 and 13 showed the least release.

     Macroinvertebrates were  identified at  all  stations (Table 12).  Stations
2, 3,  and 4 showed virtual absence of macroinvertebrate taxa.   High numbers of
the tolerant Oligochaete, Tubifex, were observed at  Station 8.  Highest diver-
                                     275

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                        TABLE 12.   MACROINVERTEBRATE DATA AT INDIANA HARBOR
HARBOR:    Indiana Harbor,  Indiana
SAMPLED:   August 30, 1977
                                             Number of Organisms for Each Taxa by Station
Taxa
                                                                                  10
                                                                                         r
                                                                                                12
                                                                                                       13
Diptera
  Chironomus             9
  Micropsectra           1
  Microtendipes          1
  Dicrotendipes          2
  Kiefferulus            2
  Procladius             3
  Brillia                1
  Chaoborus
  Chryptochironomus
  Trichocladius
01 igochaeta
  Tubifex               77
  Limnodrilus           44
  Peloscolex             3
  Branchiura sowerbyi
  Unidentifiable immature
                              210
                              281
                               23

                               45
               59
               20
              76
              95
              43

              24
             1,400
               290
               650
                10
               150
              27
               5
               9
             43
              4
             20

             30
             176
              25
              51

              35
               375
                                                         25
                      31
Hirudinea
  Glossiphonia
  Macrobdella
  Haemopis
  Helobdella

Amphiopoda
  Gammarus
Pelecyopoda
  Pisidium
  Sphaerium
  Muscueium
                                            17
                                                    41
                                                    17
                                         35
                                                              85
                                                              15
Gastropoda
  Lymnaea
  Physa
  Goniobasis
  Helisoma
                                     21
                              16
                               2
                            2
                           48
Total # of organisms
Total # of taxa
143
 10
11
 5
560
  5
114
  5
260
  7
2576
   9
99
 7
135
  6
306
  9
402
  4
171
 15
                                                    282

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sity  of  organisms  was  measured  at  Station  13.   High  diversity  and  higher
numbers of Pelecepods and  Gastropods  may be attributed  to  suitable fine sand
substrate and lower  bottom sediment contaminant levels  at  this location.

     The bulk sediment  chemistry,  PCB (polychlorinated biphenyls),  and pesti-
cides  results  show  all compounds  except  PCBs  were  below the  laboratory's
detection  limits  (Table 13).   The  detection limits  for some  compounds  were
higher than  usual due  to  high  interferences present  in  the samples.   Low PCB
concentrations were  detected  at Stations 12 and 13.   Elevated  levels of PCBs
were  found  at Station  1,  and Stations 6 through  11.  High concentrations  of
PCBs ranging from 17.9 mg/kg to 25.7 mg/kg were detected at Stations 2 through
5.

                        CONCLUSION AND RECOMMENDATIONS

     In April 1978,  the Region V office  of  the  U.S.  Environmental  Protection
Agency issued the following position on maintenance dredging of Indiana Harbor
(3):

     Analysis of Indiana Harbor indicated that bulk sediment concentrations  of
toxic  constituents   such  as  polychlorinated  biphenyls  (PCBs),  polynuclear
aromatic  hydrocarbons  (PAHs),  mercury,  lead,  arsenic,  cadmium,  and  chromium
and  nutrient concentrations   are  all  high.   Elutriate  testing shows  large
releases  of  total  Kjeldahl  nitrogen  (TKN), ammonia,  iron,  manganese, nitrate
and  nitrite,  phenols,  zinc,  and aluminum  from  virtually  all  samples.   Some
releases of  cyanide,  arsenic,  chromium,  copper,  mercury, and  nickel  are also
indicated.

     There are  three municipal  drinking water  intakes  within  three  miles  of
the Indiana  Harbor  mouth.   PCB levels in Lake Michigan are already at problem
levels,  and  Lake Michigan  is experiencing eutrophication  problems,  particu-
larly  in the  southern  end.   Utmost   care  will  have to  be taken to  ensure
against adverse environmental  health  effects  from  release of toxic and carci-
nogenic substances  due  to  dredging and subsequent  disposal  of  sediments from
Indiana  Harbor.   Consequently,  the following contingencies  must be incorpor-
ated  into  proposed  plans  for dredging  and  disposal  of  bottom sediments for
USEPA approval of  the proposed action.


DREDGING AND  DISPOSAL REQUIREMENTS

     1.   The dredging  must  not result in any increase  over background water
          concentrations (on whole-water, unfiltered sample basis) as  measured
          between the inner U.S. lights (when dredging upstream of that point)
          for mercury,  lead,  arsenic, cadmium,  chromium,  cyanide,  PCB, PAH,
          TKN,  ammonia, nitrate  and  nitrite,  total  phosphorus,  BOD  (bio-
          chemical  oxygen demand),  phenols,  copper, zinc, aluminum, chloride,
          and oil   and  grease.   When  dredging   downstream  of  the  inner U.S.
          lights, these  same limitations  should be  applied as measured between
          the ends of the outer breakwaters.

     2.   Dinn'nrj dredging,  no visible  debris or nil slick should extend beyond
          the ends of the outer breakwaters at  any time.

                                     283

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     3.    The dredging should not result in any increase over background water
          concentrations for whole-water,  unfiltered  samples taken in the raw
          water of the  three  drinking water intakes  for the parameters cited
          in item  1 above.

     4.    The U.S.  Army Corps  of  Engineers (COE)  should  consult  with appro-
          priate  sources  to arrive  at  a proposed  dredging  method  which will
          meet the dredging requirements.  It should be substantiated, through
          modeling  and  a  test  situation,  that  the proposed  dredging method
          will meet the  dredging requirements.

     5.    In  order  to determine whether the proposed  method of  dredging  is
          likely  to  meet the dredging  requirements,  the  dredging contractor
          should  test dredge  at typical  levels  of  production  in  the  area
          upstream of the inner U.S.  lights.  Dredging should then be suspend-
          ed until sampling  results are reported and reviewed.

     6.    Disposal operations must include chemical fixation of sediments.  An
          investigation will have to be conducted to determine the most effec-
          tive stabilizing  agent and optimum dosage for the type of sediments
          involved and the environmental  conditions that will  be encountered.

     7.    Disposal operations must include construction of another containment
          facility within  the existing  inland  facility.   The  inner facility
          would have  to  be  designed to  be  impermeable, with a weir and what-
          ever  controls  for  treatment  may be  necessary  for effluent  dis-
          charges.  The inner facility  should  be large enough to retain sedi-
          ments without discharge until applicable water quality standards can
          be met.   Water quality should  be monitored in the area  between the
          two  dikes,  as  well   as  outside  of  the existing  (outer)  facility,
          during  disposal operations.  An initial disposal  testing period must
          be  established to  determine  the effectiveness  of the  inner-dike
          system.

     8.    Depending on  the  type of  disposal method selected,  a  water quality
          monitoring plan will have to be developed for the disposal area.

     The  U.S.  Army Corps  of  Engineers  and  the  U.S.  Environmental  Protection
Agency are  currently  reviewing  these recommendations as well as other options
for maintenance dredging  of Indiana  Harbor.  An alternative disposal  site  is
also under consideration.
                             SAGINAW RIVER AND BAY

     During 1977, an overview of PCB contamination in the State of Michigan of
Saginaw River and  Bay  was presented at the  Third U.S./Japan Experts'  Meeting
on Management of  Bottom Sediments Containing Toxic Substances  (6).

     The presence  of PCBs  in  the  Saginaw River and Bay  resulted  in contami-
nation  of  fish  populations.  The Michigan Department  of  Agriculture detected
PCB levels  in channel  catfish  in excess of the U.S.  Food and Drug Administra-
tion tolerance 'eve! of 5 mg/kg.  As a result, a ban was issued for commercial

                                     285

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catfishing in trie  inner  Saginaw Bay area.  The continued detection of PCBs in
Saginaw Bay fish indicated that PCBs previously released to sediments continue
to be detected in resident fish populations.

     In  view  of  existing PCB  problems  in  Saginaw River  and Bay,  the  U.S.
Environmental  Protection Agency was unable to concur with proposed maintenance
dredging and disposal  in  1976 until a  complete  sediment  analyses program for
PCBs was undertaken.

     The U.S.  Environmental  Protection  Agency  (Chicago Office)  and the  U.S.
Army  Corps  of  Engineers  (Detroit  District)  conducted an  intensive survey of
Saginaw  River and  Bay  in  October,   1976.  PCBs were sampled at 35 locations in
Saginaw  River  and  at  11  locations  in Saginaw  Bay.   PCB  concentrations in
bottom  sediments  ranged   from  <0.1  to  22.9 mg/kg  for  all  locations.  Samples
taken in the downstream  vicinity of the  City  of  Saginaw Wastewater Treatment
ranged  from 5.5 to 22.9 mg/kg PCB.   PCB concentrations  near the Bay City Waste
Water Treatment  Plant  ranged  from 3.5  to  11.8 mg/kg.  Sediment  samples ob-
tained  in  Saginaw  Bay  had considerably  lower  PCB  concentrations  ranging  from
1.3 to 4.2  mg/kg.

     During 1978,  the  U.S.  Environmental Protection Agency requested that the
Michigan Department  of Natural  Resources  review  the  two  PCB-affected areas,
downstream of  the Saginaw Wastewater  Treatment Plant  and  in  the vicinity of
the  Bay  City Wastewater  Treatment  Plant.  The Department of Natural Resources
indicated  that  a  metal casting plant  in  the Saginaw area  and  an automotive
motor facility in  Bay City were possible sources.  Both facilities had hydrau-
lic  systems  that were   previously  contaminated  with  PCBs.   PCB  hydraulic
fluids  were  initially  flushed  at  both plants in  1971  and  were  replaced  with
PCB-free hydraulic fluids.  Samples from the two facilities and the wastewater
treatment plants are  currently being analyzed.

     During  1978,  maintenance  dredging  was  conducted  at  the  Saginaw River
channel  by the Detroit District Corps  of Engineers.  Dredging was accomplished
by  the  Hopper Dredge  HAINS  from  areas of  low  level  PCB  contamination   (<10
mg/kg).   Dredged  materials were disposed of  in  the Middle  Grounds Disposal
Site  in  Bay  City,  Michigan.   It has been proposed that subsequent dredging of
more  highly  contaminated  areas  will   use  the  recently completed  Saginaw Bay
Dike Disposal Facility.


                                  REFERENCES

1.   Kleinert,   S.  J. ,  T. B.  Sheffy,  J.  Addis,  J.   Bode,  P. Shultz, J.  J.
     Delfino, and  L.  Lueschow.   Final  Report on the Investigation of PCB's in
     the Sheboygan River System.   Department  of  Natural  Resources, Madison,
     Wisconsin.   1978.  51 pages.

2.   U.S.  Environmental  Protection   Agency,  Region  V,  Chicago,  Illinois.
     Sheboygan Small Boat Harbor, Wisconsin,  Report on the Degree of Pollution
     of Bottom  Sediments.  1977.  9  pages.
                                     286

-------
3.
4.
5.
6.
U.S.   Army  Corps
Impact  Statement
Harbor, Indiana.
 of  Engineers,
 on  Operation
1977.  40 pages.
Chicago  District.   Final  Environmental
and  Maintenance Activities  at  Indiana
U.S.   Environmental  Protection  Agency,  Region  V,  Chicago,  Illinois.
Indiana  Harbor,  Indiana,  Report on  the Degree  of Pollution  of Bottom
Sediments.   1977.   17 pages.

Alexander,  G.  R.  Letter  to Howard N. Nicholas,  U.S.  Army Corps of Engi-
neers, Chicago District Office.  April 19,  1978.

Bremer, K.  E.  An  Overview of Bottom Sediment  Problems  in Saginaw River
and Bay, Marinette-Menominee Harbor, and Waukegan  Harbor.  Presented at
the Third  U.S. Japan  Experts'  Meeting  on Management  of  Bottom Sediments
Containing  Toxic  Substances,  Easton, Maryland,  1977.   17 pages.
                                    287

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          DEVELOPMENTAL ASPECTS AND CURRENT POLICIES FOR RESTORATION
                  AND PROTECTION OF PUBLICLY OWNED FRESHWATER
                          LAKES IN THE UNITED STATES

                                      by

                              Spencer A.  Peterson
                  Corvallis Environmental Research  Laboratory
                     U.S.  Environmental  Protection  Agency
                             Corvallis,  OR  97330

                                      and

                               Robert J.  Johnson
                        Criteria and Standards Division
                     U.S.  Environmental  Protection  Agency
                            Washington,  D.C.   20460
                                   ABSTRACT

     Some historical  aspects  of  the impact of pollution on lake water quality
in the United  States  are discussed.  The results of two nationwide lake water
quality surveys are addressed and the development of the United States Govern-
ment's involvement  in water pollution control is  traced  from 1912.   Although
restoration  of degraded  lakes   and  protection  of higher  quality lakes  was
authorized by  the  Federal  Water  Pollution Control  Act Amendments of 1972, the
"Clean Lakes Program"  received relatively low priority for almost seven years.
Other, more  geographically pervasive  pollution  control programs  were deter-
mined  more   important.   In fiscal  year  1979,  as   a  result of  strong public
demand,  the  Environmental  Protection Agency  sought  funds  and  positions  to
support  the program.   Thus,  the  formulation of  National   Lake  Restoration
policy in the  United States has  been gradual.  A regulation is proposed by the
EPA,  Office  of Water  Planning  and  Standards  to  facilitate  more  uniform and
equitable administration of the Clean Lakes Program.

                                 INTRODUCTION

     The United States has more than 100 thousand lakes ranging in size from a
few hectares to  Lake  Superior at 8.41 x  106 hectares.  The State of Minnesota
is  known  as  "the land of  10,000 lakes"  which is  really a  misnomer  since the
state actually has somewhat in excess of  13,000 lakes.  In the past,  the large
number of lakes  in  the United States  has  produced a certain amount of apathy
among their  users.   The attitude has  been that  lakes were there  to  be used,
and Americans  have  used  them with little  regard for  their sometimes  delicate
ecosystems.   Lakes  have served  as  drinking water supplies and  for  fishing,
                                      289

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swimming,  boating  and  various  other  recreational  uses.   Unfortunately  they
have also  served as  convenient  recipients of municipal  and industrial  waste-
water.

     Historically,  the  latter uses  primarily  impacted  urban  lakes;  however,
the problem of  water  quality degradation of both urban and rural  lakes became
more pronounced  in the  United  States after 1945 when  phosphate-based deter-
gents were  introduced.   Within  a  few years the phosphorus content of domestic
wastewater doubled and  the  adverse effect on urban lakes  became  more severe.
About the  same  time,  Americans  began to enjoy  new freedoms  through  improved
working  conditions and  reduced working  hours.   A 40-hour work week  became
commonplace as did the private ownership of automobiles.  Largely due to these
two factors, coupled with the introduction of phosphate detergents and larger,
more concentrated  populations,  the problem which had  been generally contained
to urban  lakes  began  to impinge on an increasing number of the Nation's small
rural  lakes.   By  1972,  92.8%  of  the  vacations and  60.9% of the  overnight
recreation  trips  in  the  United  States  involved  round trips of  400  miles or
more  (USDA,  1973).   Reduced  working  hours  meant  increased  leisure  time.
Privately  owned cars  brought greater  mobility  and  higher  living  standards
permitted  second  home ownership for many.   Lake fronts  were among  the  most
popular  locations  for  these  second homes.   By the mid 1950's cabins and homes
completely ringed the shorelines of many previously  remote and pristine lakes.
Too  frequently,  the  wilderness weekend  retreat was  simply an  extension of
everyday  urban  and  surburban living.   The  weekend  recreationist washed  his
car, clothes, dishes,  etc.  with high phosphate detergents, flushed his modern
toilet and otherwise overloaded inadequate septic wastewater treatment facili-
ties, thus  promoting the  flow  of  enriched groundwater  to  local  lakes (Ellis
and  Childs,  1973;  Dudley and Stephenson,  1973).  Lakeside  lawn  fertilization
and gardening also produced  adverse  effects.   The situation worsened as life-
styles  continued  to  change  and  increasing numbers  of people made  lakefront
homes their primary residences.   Recreational  experiences became a way of  life
in the United  States.

     Recreation was  not  the  only cause of  small-lake  water quality problems.
Intensified agricultural  practices  contributed  nutrients,  pesticides,  herbi-
cides,  and  silt to the Nation's freshwater streams and lakes.   The overabun-
dance  of plant  nutrients,   however,  is  'the most  evident  of  these  problems,
since the nutrients support massive growths of algae and rooted aquatic plants
which hamper the recreational  uses of lakes.

                       EXTENT AND NATURE OF THE PROBLEM

     The fact that a declining water quality condition in lakes was associated
with  increased  use  of  phosphorus-based detergents  and  intensified  farming
practices  was  not  coincidental.  There  is  abundant literature  to demonstrate
highly  significant correlations  between  algal  concentrations in lakes and the
phosphorus  content of  phosphorus-limited water.   An  excellent coverage of the
subject is presented  in a paper by Nicholls  and Dillon (1978).

     In  1971 Ketelle and Uttormark (1971) surveyed problem  lakes of the United
States.   Their primary objective was to identify those lakes that had deterio-
rated  so much  that  rehabilitation  would  be  required  if  satisfactory water
                                      290

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quality was to be re-established.  Forty of the 48 contiguous States responded
to questionnaires  distributed by  the  University of  Wisconsin.   Through this
process, approximately 400  problem lakes were identified.  That number cannot
be considered  indicative  of the  problem since some States failed to reply (no
lake problems)  while others  submitted  extensive lists  (49 problem  lakes  in
Florida).   Another problem with the survey was that it left individual respon-
dents with the  responsibility for determining which lakes had deteriorated to
the extent that restoration would be required.

     The survey conducted  by Ketelle and Uttormark did  point  out a number of
significant factors.  Of  the  40  States  that responded,  35  indicated  they had
some lakes with severe  water quality problems (Table  1).   This  indicates the
problem was  widespread.   Although  10  different  problem  types were listed by
various States, the  two  most frequently cited were nuisance algal  blooms and
nuisance rooted aquatic  plants.   The most frequent problem source was munici-
pal effluent  (a point  source),  cited nearly 2 to  1  over the next most common
individual problem  source.   When  taken  collectively,  however,  the non-point
source problems were  cited more frequently than  the point  source problems.

     Another water quality  survey was initiated in early 1972 by the Environ-
mental  Protection  Agency.   This  survey  stemmed  largely  from  the then active
controversy over  the removal  of phosphates from detergents due  to their al-
leged  adverse  impact on  freshwater lakes  and reservoirs.   The  objectives of
the National  Eutrophication  Survey  (NES) were to:

     (1)  Identify those  lakes and reservoirs  in the contiguous United States
          that received nutrients from discharges of municipal  waste treatment
          faci1ities.

     (2)  Determine  the  effect  of  those point  source nutrient  inputs on the
          nutrient levels and primary productivity of the  water  bodies,  and

     (3)  On the basis  of the survey information, to  advise the Construction
          Grants Program  (building of wastewater treatment facilities) on the
          cost  effective  allocation of Federal  funds  for the  construction of
          tertiary waste treatment facilities for phosphorus removal.

     Under these guidelines  the  NES sampled 401  lakes east of the Mississippi
River  and  not  surprisingly  found that 78% of them were eutrophic according to
the  6  parameter trophic classification  system  (total  phosphorus, chlorophyll
a,  Secchi  depth,  dissolved  orthophosphorus,  inorganic  nitrogen  and hypolim-
netic  oxygen  saturation percentage)  used by NES  (USEPA,  1974).  West of the
Mississippi River the  objectives of the  survey  were  broadened to assess non-
point  source  (NPS)   contributions  of nutrients  to the lakes and  to assist in
establishing  water  quality  criteria  for  nutrients  (All urn,  Glessner  and
Gakstatter, 1977).  After sampling 374 lakes in the western United States, the
National Eutrophication Survey determined  that 72% were eutrophic.

     Lakes  contribute  substantially  to  the economy  of   states  which promote
water-oriented  recreation.   Although  accurate   cost  figures are  not readily
available  it  is evident  that eutrophication and water  pollution impairs the
water-oriented  economy  of these  areas  due to lower property  values,  cost of
                                      291

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restoring  or  managing  the  lakes,  and  their  generally  reduced  usability.
Bartsch  (1972)  indicated  in  1972  that the  loss  amounted to  several  million
dollars per year.  This  figure no doubt has increased substantially since that
time.

                       LEGISLATION AND CONTROL PROGRAMS

LEGISLATION

     The U.S.  Federal Government's  involvement  in the water  pollution control
field dates  back  to  1912  and has its roots in the U.S.  Public Health Service.
There was  limited activity  in  this  area,  however,  until 1948 when  the  Water
Pollution  Control  Act of  1948  required the Public Health Service  to provide
technical  information to  States.  Even  then pollution  control  measures were
not of  high  priority  at  the Federal level.  A series of Congressional Acts up
through  1956 established  public  support  for  Federal  responsibility  in this
area, but  the Acts were  generally  ineffective.  According  to  Reitze (1972),
"The new  Acts were designed to be unenforceable (industry  doesn't  want con-
trol, the  public does.   Compromise^   Pollution  control laws  for  the public,
unenforceability  for  industry.)".  The  Water Pollution Control Act Amendments
of 1961  (P.L. 87-88,  1961)  were significant with regard to  the Federal Govern-
ment's   involvement in water  pollution control since the Amendments authorized
the  establishment,  equipping,  and  maintaining  of  field laboratories  at  7
locations  in the  United   States.  One  of those  laboratories  was  located at
Corvallis, Oregon.

     Finally  in  1965, the  Water Quality Act  (P.L.  89-234, 1965) provided the
enabling  legislative  framework  to remove the responsibility  for water pollu-
tion control  activities  from  the  Public  Health Service and to  establish  the
Federal   Water Pollution  Control  Administration  (FWPCA).   Reitze  (1972)  has
pointed  out  that the Federal  Water  Pollution  Control  Administration's  chief
concern became the dispensing of large amounts of Federal dollars to construct
sewage   treatment plants.    Approximately  90%  of  their  budget went  for this
purpose; only 10% supported the administration,  enforcement programs, research
and development,  planning,   training  and  technical  assistance  activities.   In
spite of  the limited  research efforts of  the Federal  Water  Pollution Control
Administration and  largely due to the  efforts  of Dr.  A. F.   Bartsch,  the  Na-
tional   Eutrophication Research  Program  was established in  1968 at what is now
the  Corvallis  Environmental  Research  Laboratory   (CERL).   This  laboratory
eventually became the focal  point for  freshwater ecological  effects research
within   the  Environmental  Protection  Agency.   Information  developed by  the
Corvallis Research Laboratory and its contractors played a  key role in shaping
the future of freshwater lake pollution control  in  the United States.

     In 1969 the public's  concern for environmental  conditions culminated in a
demand   for action by the U.S. Congress.  Several pieces of  new legislation and
modifications  of older  legislation  began to appear.   The  Water  Quality  Im-
provement  Act of 1970  (P.L.  91-224, 1970)  allowed conversion  of  the Federal
Water Pollution  Control Administration to the  Federal  Water Quality Adminis-
tration (FWQA), which, in  1971, became part of the newly created Environmental
Protection  Agency (EPA).    About  that  same  time  the  National  Eutrophication
Research  Program  at CERL  was upgraded to the National  Eutrophication and Lake
                                      292

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Restoration Program.  The first lake restoration research project to be funded
by  EPA  under this  program  was  located at Shagawa  Lake,  Minnesota  (Malueg et
al_.  1973) where  a  full-scale advanced wastewater treatment  system  was built.
It was  designed  to  remove phosphorus from domestic wastewater down to a level
of 0.05 mg/1.  In 1972 Congress passed the most far-reaching piece of legisla-
tion  to  date concerning  water  pollution control measures,  the  Federal  Water
Pollution Control Act Amendments of 1972 (PL 92-500, 1972).  The most signifi-
cant  aspect  of  this  law with  regard  to lakes  was Section  314  which states
that:

     A.    Each State  shall  prepare or establish, and  submit to the
          Administrator  (of  the  U.S.  Environmental  Protection Agen-
          cy) for his  approval

          1.    An  identification  and  classification  according  to
               eutrophic  condition  of  all  publicly owned freshwater
               lakes in such State;

          2.    Procedures,  processes,  and  methods   (including  land
               use requirements), to control sources of pollution of
               such lakes; and

          3.    Methods and procedures,  in conjunction with appropri-
               ate  Federal  agencies, to  restore the quality of such
               lakes.

      B.  The  Administrator  shall  provide financial  assistance  to
          States in  order  to  carry out methods  and procedures ap-
          proved by him under this section.

     The  law  further  specified  that the amount granted  to  any  State for any
fiscal  year  to  conduct  approved  methods  and  procedures under  this section
would not exceed 70%  of the  total  project  cost.  The  Act authorized $50 mil-
lion  for  the  fiscal year ending June 30, 1973, $100 million for 1974 and $150
million  for  1975  for  grants  to States  to conduct work to comply  with the
various provisions  of  the law.

     A number  of other sections of the 1972 amendments to the Act would even-
tually impinge on  lake water quality.   One of  the  most  important was Section
208 which required  the  development  of  areawide waste  treatment  management
plans.  It  specified  that  States  would  identify areas which,  as  a result of
urban  and industrial  concentrations  or  some  other  factor,  had substantial
water quality  problems.   It directed  the States  to  then  develop  an organiza-
tion  which  would  put  into operation a  continuing areawide  waste treatment
management planning process.  This  program  would be comprehensive in coverage
of pollutant types  and sources,  but it  identified  specifically that agricul-
tural  and si 1 vicultural  related non-point  sources  of  pollution be identified
and that,  to the extent feasible, methods be set forth to control  the problem.
The approach  of  dealing  with these and other  non-point  sources  of pollution
coincides with  the most  frequently cited  problem  sources  shown  in  Table 1.
Therefore, the Section  208  program will  eventually  have  a significant impact
on a  number  of freshwater lakes, particularly  those in urban settings.  While
                                      293

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                 TABLE  1.   PROBLEM  LAKES OF THE UNITED STATES SHOWING FREQUENCY OF PROBLEM TYPES
                           AND  SOURCES  OF  POLLUTANTS  (Modified from Ketelle and Uttormark, 1971)*

Lake Location
(State)
























Arkansas
Cal ifornia
Colorado
Connecticut
Delaware
Florida
Georgia
11 1 inois
Indiana
Louisiana
Maine
Maryland
Massachusetts
Michigan
Minnesota
Missouri
Nebraska
New Hampshire
New Jersey
New York
North Dakota
Ohio
Oklahoma
Oregon
Pennsylvania
South Dakota
Vermont
Vi rginia
Washington
Wisconsin
Totals

Total Surface
Area Impacted
(ha)























1,214
167,552
4,431
1 ,801
1 ,158
251,519
2,108
2,590
2,551
274,082
11,111
32
2,229
7,596
21,659
392
1,096
1,813
2,562
76,295
645
10,013
28,634
41 ,621
10,220
18,430
120,823
1 ,358
10,747
87,872
1,164,154

Number of Lakes
Impacted
























1
4
4
8
41
49
2
1
29
11
21
1
23
24
29
1
3
2
26
10
2
11
4
3
14
10
3
4
19
34
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Those states not reporting the number of surface acres  impacted  or  the  nature  and  source  of  the  problems  were
omitted from the original  table by Ketelle and Uttormark.
                                                     294

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the Areawide Waste  Treatment  Management Program will be important in protect-
ing, and to  some  degree restoring, lakes by limiting the input of pollutants,
the Section  314 Clean  Lakes Program will be primarily responsible for restor-
ing degraded lake systems  to  an acceptable level and  protecting others from
degradation.

CONTROL PROGRAMS

     Section 314  of PL 92-500  is  known as  the "Clean  Lakes  Section"  and the
EPA program  associated  with it has come to  be known as the "Clean Lakes Pro-
gram".   Basically,  it  is a Federal/grantee cost  sharing  program designed to
improve the  water quality  and general  usability  of the  Nation's  freshwater
lakes.   The  program,  historically,  has  received a relatively  low priority
ranking among  what  the Environmental   Protection  Agency has  considered more
critical programs.   Among these are the Construction Grants  Program to build
waste  treatment plants,  the Areawide Waste  Treatment Management  Program, the
development  of  effluent  guidelines to  control  industrial discharges, and more
recently the Toxic Substances Control Program.

     EPA entered  the lake  restoration  field in FY 1975 when Congress indepen-
dently  appropriated  $4 million  for expenditure on  the Clean  Lakes Program.
EPA's Office of Water Planning and Standards was charged with dispensing these
funds for public use.


          POLICIES FOR RESTORATION AND PROTECTION OF FRESHWATER LAKES

EARLY POLICY AND LEGISLATIVE AMENDMENT

     Policies for implementing the Clean Lakes Program have evolved gradually.
One of  the  first  policy decisions concerned the  Federal/grantee  cost sharing
fractions.    Although  authorized by Section  314 of  the  law  to Federally fund
lake restoration  projects up  to 70%,  the Environmental  Protection Agency made
an early decision  to  limit such funding  to 50% of the total  project  cost.

     Another early  problem  was the fact that EPA did not have a funding mech-
anism to disperse funds appropriated  under  the authority of  Section 314.  The
Agency  did  have,  however,  an  established regulation to  support  research and
demonstration grants.  Therefore a policy was established to fund lake restor-
ation projects through that mechanism.   This decision eventually caused a good
deal of confusion and will   be addressed later in this paper, however, it was a
most reasonable decision at the time considering the state-of-the-art of lake
restoration.   Lake   restoration  technologies were  predictable gualitatively,
but not quantitatively;  that  is, the direction of water quality change caused
by applying a certain technology was known, but  not  the degree of change.

     Another  significant   decision  by  the  Agency  was  to  make   a  portion
($400,000)  of  the initial  $4 million lake restoration appropriation available
to  the  Office  of  Research   and Development to assess the overall effectiveness
of  various  lake  restoration techniques being used in the Clean Lakes Program.
Responsibility for this aspect of the program was transferred to the Corvallis
Environmental  Research  Laboratory where scientists  developed an  experimental
                                      295

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design to accomplish tne objectives of the evaluation program.   Tne design was
approved  by  the  Office of Water  Planning and  Standards  and  implemented  in
conjunction with the lake restoration program.   Descriptions of the experimen-
tal  design  and approaches to the  evaluation  program have been reported  in  a
number  of  papers  (Porcella   and  Peterson,   1977;   Porcella,  Peterson  and
Glessner, 1977; Peterson, 1978;  Porcella,  Peterson and Larsen,  1978; and Honey
and Hogg, 1978).

     The  early policy   for  reviewing grant  applications  is   illustrated  in
Figure 1.  According to  this  procedure,  the applications had to be consistent
with State and Federal areawide water quality planning programs.  All applica-
tions were reviewed by the Office of Water Planning and Standards  (OWPS) staff
members,  at  least two  university  consultants,  and  by a staff member  of the
Corvallis  Environmental  Research Laboratory  (representing  the Office  of Re-
search and Development).  The  review panel, consisting of members  from each of
these groups as well  as EPA's Regional Office  Lake  Restoration Coordinators,
met when  deemed necessary  by  the Office of Water Planning and Standards.  The
merits and demerits  of  each  proposal  \*ere discussed  and  the committee made  a
decision  to either  fund,  reject  or request additional  information  on a given
proposal.  In  late  1975 a  number of  projects  were  funded  using  this  review
process and the initial $4 million appropriated for the program.

     In  1976,  the  Office of  Water Planning and  Standards received another $15
million from Congress to meet  the growing demand for lake restoration dollars.
Again, part  of these  funds  ($1,500,000)  were  provided to  the Office  of Re-
search and Development  for  evaluation projects.  In 1977,  Congress reaffirmed
its commitment to the  Clean  Lakes  Program by amending Section 314 of  Public
Law 92-500.  The Clean Water Act of 1977 (P.L.  95-217, 1977) extended the time
frame of  the program through  Fiscal Year  1980  and  authorized  $50 million for
it  in  1977 and an additional  $60  million  per  Fiscal Year  for  1978,  1979 and
1980.   The amendments under Section 304(j) also required the Administrator of
EPA to  issue biennially updated  "procedures and processes as may be appropri-
ate to  restore and enhance the quality of the  Nation's publicly owned fresh-
water  lakes"  (PL  95-217,  1977).   In  1977, Congress  appropriated  another $15
million for program operation.   The Agency now had a $34 million  program.

     In  1978 the  Congress  looked at the needs  of  the Clean Lakes Program and
trimmed  its funding  level  to  $2.3 million.  A major reason for this reduction
in  funding was that the program had  not  obligated  several  million dollars of
the previous year's budget.  What  the Congress did  not realize  was that all
the  funds had  been committed.   As  of  April   24,  1978,  65  lake  restoration
projects  in  21 states  had been  funded (Table  2).   During August  1978,  the
first National  Conference  on  Lake Restoration was sponsored by EPA and hosted
by  the State  of  Minnesota.   The  conference  attracted over 450  participants
from  39  states and  Canada.   Increasingly it has become  apparent  that "Clean
Lakes" is  a  broadly based,  grassroots supported program  that  has high poten-
tial for  dramatic pollution control and water quality improvement of lakes and
their tributaries.

     During  the  FY-79  budgeting  process  the  Agency made  its  first  formal
request  for  funds and  positions to  support  the program.   EPA asked for and
received  $15 million and  15  positions.    Of greater  significance  however was
                                      296

-------
           STATE AND/OR LOCAL APPLICATION PREPARATION
                              I
               STATE GOVERNMENT CLEARING HOUSE
                   EPA GRANTS ADMINISTRATION
                              I
           EPA OFFICE OF WATER PLANNING AND STANDARDS
                         REVIEW PROCESS
   OFFICE OF RESEARCH
    AND DEVELOPMENT
           UNIVERSITY
           CONSULTANTS
                              I
 OFFICE OF WATER
PLANNING AND STDS.
                         REVIEW PANEL
         1
      RETURNED FOR
    ADDITIONAL INFO.
     i
REJECTED ON
SECOND ROUND
     i
  FUNDED ON
SECOND ROUND
                             REJECTED
                   MONITORING OF RESTORATION
                 GRANT BY EPA REGIONAL OFFICE
         Figure 1.  Clean Lakes application procedures.

                          297

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TABLE 2.   CLEAN LAKE  PROJECT  SITES, FEDERAL FUNDING LEVELS, AND DATES OF THE INITIAL AWARDS

State
California
n
n
n
Florida
n
11 1 inois
Indiana
Iowa
ii
Maine
Maryland
Massachusetts
n
n
n
Michigan
ii
Minnesota
n
n
n
n
n
Missouri
M
n
New York
n
n
M
II
II
II
II
North Carolina
Oklahoma
Oregon
Lake
Stafford*
Temescal*
Lafayette
Ellis*
Jackson
Apopka
Frank Holton*
Skinner
Lenox*
Oelwein*
Blue*
Little Pond
Annabessacook
Lock Raven
Morses Pond*
Charles River
Cochituate
Ellis Brett Pond*
Lower Mystic
Nutting*
Lansing*
Reeds
Long*
Phalen
Albert Lea*
Clear
Chain of Lakes
Hyland
Penn*
Vandal ia*
Finger
Rothwell*
Ronkonkoma
Delaware Park*
Tivol i
Hampton Manor*
Collins Park*
Steinmetz*
Buckingham*
Washington Park*
59th Street Pond*
Mystic*
Pauls Valley
Commonwealth*
Grantee/Location
Novato
Oakland
n
Marysvi 1 le
Tal lahassee
n
E. St. Louis
Ft. Wayne
Lenox
Oelwein
Onawa
Damariscotta
Winthrop
Baltimore
Wei lesley
Boston
Natick
Brockton
Boston
Billerica
Mason
E. Grand Rapids
Arden Hills
Minneapol is-St. Paul
Albert Lea
Waseca
Minneapol is
Maple Run
Bloomington
Vandal i a
Col umbia
Moberly
Islip
Buffalo
Albany
E. Greenbush
Scotia
Schenectady
Albany
n
New York City
Lake Lure
Pauls Valley
Beaverton
Amount
$ 290,250
244,486
49,250
1 ,375,000
302,834
215,734
927,000
403,496
100,000
59,490
372,500
11,710
278,020
110,000
308,740
296,700
125,000
106,500
320,000
166,211
1,255,957
903,452
1,296,715
575,683
302,800
269,075
179,000
161,198
87,900
350,000
50,000
45,000
334,048
141 ,500
121,500
50,000
79,355
36,680
23,250
II
325,020
21,080
300,000
53,200
Date of First Award
04/08/77
03/31/77
03/21/77
05/20/77
08/31/76
01/06/76
03/16/77
09/17/76
03/08/77
03/11/77
11/10/77
02/19/76
08/01/77
04/07/77
08/23/76
09/16/76
08/26/76
01/05/77
11/21/77
05/12/77
04/13/76
06/29/77
12/18/76
01/18/77
01/08/76
09/27/76
02/13/76
08/10/76
03/21/77
02/06/78
02/16/78
02/16/78
09/29/76
02/17/76
04/11/77
04/09/76
01/08/76
12/30/76
04/09/76
H
05/12/77
09/30/77
08/16/77
12/21/76
                                                                                    (continued)
                                             298

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TABLE 2 (continued)
    State
                        Lake
Grantee/Location
                                                                  Amount
                                                                              Date of First Award
South Dakota
ii
11
"
Texas
Vermont
Virginia
Washington
H
M
II
II
II
II
Wisconsin
ii
H
11
N
n
H
Kampeska
Swann
Oakwood
Cochrane
McQueeney*
Bomoseen
Ri vanna
Liberty*
Long*
Moses
Spada/Chaplain
Medical
Vancouver*
Sacajawea*
Little Muskego*
Half Moon
Lilly*
Mirror/Shadow
Noquebay
Henry*
White Clay
Watertown
Viborg
Brookings
"
Sequin
Castleton
Charlottesvi 1 le
Spokane
Port Orchard
Moses
Everett
Medical Lake
Vancouver
Longview
Wheatland
Eau Claire
Wheatland
Waupaca
Marinette
Blair
Madison
$ 67,000
39,500
26,500
9,906
120,000
74,640
39,728
577,975
355,970
124,675
99,000
128,217
25,000
1 ,717,562
995,000
371 ,500
273,000
215,000
245,000
220,000
107,200
08/25/76
12/07/76
08/10/76
01/08/76
11/15/77
06/15/77
03/23/77
02/07/77
01/08/76
08/31/76
01/08/76
12/21/76
08/23/76
01/06/78
08/10/76
01/18/76
01/08/76
1)
08/23/76
12/21/76
01/08/76

  Notes projects which include dredging or  sediment  treatment.
                                              299

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the decision  to seek permission from  the  Office of Management and  Budget to
develop a regulation to establish policies  and procedures for grant assistance
to the States in conjunction with Section 314 of the Clean Water Act.  Permis-
sion  was  given  and regulations  concerning  grants  for  the restoration  and
protection of lakes  in the United States are now being developed.

INITIAL PROGRAM  GUIDANCE

     At the  outset  of  the Clean Lakes  Program in 1975,  there was  no assurance
of its viability.   It was a relatively small (first year  funding was $4 mil-
lion)   program with  what appeared  to  be  limited  and   somewhat  regionalized
support.   Therefore, instead of  adopting new regulations and gearing up for a
new program,  it was decided to  operate  within the existing  framework  of EPA
grant  regulations.   As  indicated previously,  the  research  and  demonstration
section of the  Act,  Section 104 (h), was selected as the funding vehicle.  It
followed  from this  that the  Clean Lakes  granting practices  would have to
comply with  the  research and  demonstration grant regulations.  This operating
procedure was adopted,  and general  guidelines were  formulated for  the prepara-
tion of lake  restoration grant applications  (USEPA,  1976).

     The  1976 Guidance  Document specified  that EPA was  most interested in
funding lake  restoration  projects which:

     1.   Employed  methods  to  restore lake water  quality by eliminating or
          otherwise restricting  the  input  of non-point  source waste influents
          to  the  lake  or that  part of  its  drainage basin where a  contributing
          pollutional effect on  the lake water quality  could be  demonstrated
          and;

     2.   Used in-lake techniques to remove  or inactivate undesirable pollut-
          ants,   including nutrients, after steps were taken  in the watershed
          to reduce their rapid re-accumulation.

     The  following  statement  from  the Guidance   Document   provides  further
evidence that the Clean Lakes  Program would stress  watershed, non-point  source
pollutant  control  technologies   over in-lake  treatment  techniques.   "Reducing
or eliminating  the  sources  of  waste loading may be  the  only restorative mea-
sure  that  is needed to  achieve the desired level of improvement  of certain
lakes" (USEPA,  1976).  The  statement has  a strong basis  if  one  considers the
percentage of various  pollutants estimated to be derived from non-point sour-
ces (Table 3).    It also  is  clear  that the program is directed  toward the
problem sources  most frequently identified  in Table 1  by  Ketelle and Uttormark
in 1971.

     The  Guidance  Document  further states  that  Clean  Lakes  funds provided
under  Section 314 wil 1  not be  used to  control  point source waste  where the
issuance of  permits  (according  to  Section  402 of the Act) or the  construction
of wastewater treatment  facilities  (according to Section 201 of the Act) will
alleviate  the causes of pollution.   The following types  of projects are  listed
as examples of those eligible for funding:
                                      300

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     TABLE 3.   ESTIMATED PERCENTAGE OF TOTAL POLLUTANT DISCHARGES WHICH
               ARE DERIVED FROM NON-POINT SOURCES (from Freeman,  1978)
                                           Non-Point Sources as
             Pollutant                Percentages of Total Discharge
          Suspended Solids                         92

          Fecal Coliform                           98

          Total Nitrates                           79

          Total Phosphates                         53

          BOD                                      37




     o    Lake drawdown and  lake bed consolidation;

     o    Use of flocculants to precipitate nutrients;

     o    Dredging or covering of sediments;

     o    Dilution and displacement of pollutants with good quality water;

     o    Purchase or  long-term  leasing  of land easements to establish buffer
          zones for the control of runoff and its effects;

     o    Diversion of nutrients and sediments from lakes;

     o    Improving agricultural  and other land use practices to keep soil  and
          nutrients in the watershed.

     Projects  considered  to be  ineligible for funding under  the  program  are
described in  a later section  of  this paper under Federal  Funding Restrictions
For Phase 1 and Phase 2 grants.

CURRENT LAKE  RESTORATION PROGRAM POLICY

     There is  little  doubt that the  intent and policies  of the  program were
designed  to  control  and reduce  non-point  source  pollutants.   The  program  was
tailored  to  complement  the Section  208  Areawide  Waste  Management Planning
Program.   In this  respect,  by  late  1977, several  States began  making requests
for Federal  assistance to  develop  technically sound  lake restoration propo-
sals.   However,  the  initial  EPA program guidelines  specifically  prohibited
Federal  funds  from being used  for  that  purpose.   The funds were  for use in
actual lake restoration implementations only.  There was a good deal of confu-
sion over the  50% Federal/50%  grantee cost-sharing policy  established by  EPA
                                      301

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for the  Clean Lakes  Program  and the  customary 95%  Federal/5%  grantee cost-
sharing policy  for research  and  demonstration grants  administered  under the
same section  of  the  law [104(h)].   Another point of difficulty arose from the
fact that Section  314 of the Act stated  that  grants  under this  program would
be  made  only to  the  States.   No other  organizations  or  governmental  levels
were mentioned.  However, Section 104  permits  grants  to go to State agencies,
local  governmental units, or any group elected by and  representing the general
public  in  areas  of   control  or regulatory  authority  over a publicly owned
freshwater  lake.   Inconsistencies   between  the  Section 314  mandate  and the
Section 104  funding  vehicle  were  making the increasingly  complex  Clean Lakes
Program difficult to manage.  While  the program had been initiated as a demon-
stration program, there was considerable pressure from States and EPA Regional
offices to convert  it to an operational program.  All of these considerations
led to  the  conclusion  that  a  new  governing regulation would  be  necessary to
establish uniform policies and procedures for administering the Clean Lakes --
Lake  Restoration Program.   The  new  regulatory/policy language  is  currently
being formulated with  the following goals in mind:

     1.    To  present  a uniform  set of requirements  to  define eligible grant
          applicants and specify the  types of projects that would qualify for
          assistance under the program;

     2.    To  provide  grant applicants with  explicit  information requirements
          to be included in all applications;

     3.    To  assist  States  in  complying with  the requirement  to  prioritize
          their lakes for restorative action;

     4.    To  define the administrative procedures used by  EPA to  receive and
          review proposals and prepare  funding recommendations; and

     5.    To  define  Federal  funding for  lake  restorative  and pre-restorative
          activities.

     The following  five sections of  this paper  and  Appendix A draw heavily
from  the  draft  regulation document  prepared  by  the  Criteria  and  Standards
Division of the  Environmental Protection Agency.  It should be understood that
this information is currently in draft form and subject to  change.  A proposed
regulation will  be made available  for a  60-day  public comment period.  After
that time the final regulation will be  developed  and promulgated.

Eligibility

     Freshwater  lake  under the draft  regulation  refers  to any  inland pond,
reservoir,  impoundment, or other similar body of water that exhibits no marine
water intrusion  as a  result  of oceanic or  tidal  activities.  The  water body
must have public recreational value and, therefore, public  access.  Reservoirs
used solely  for drinking  water  supplies are prohibited  from  receiving funds
under this program.   In accordance  with Section 314 of the Act,  the new regu-
lation would  allow grants  to  be made  only  to States.  However,  it would be
permissible for the States to enter  into interagency agreements with sub-state
entities (county,  township,  municipality, city, watershed  district,  etc.) to
                                      302

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perform various  tasks included  in  the scope of work  of  specific grants.   In
other words,  suD-state entities  could act as  sub-contractors  to the States.
All  such  sub-state interagency  agreements  would  be  reviewed by  the EPA  Re-
gional Administrator  and  subject to his approval  if  the  sum of the agreement
exceeded $100,000.

     The  types  of projects  eligible  for funding  will  remain essentially  the
same  under  the  new  regulation  as they had been under  the  initial  program
guidance  document.   One  significant   exception  will   be  mentioned  under  the
following section  on   types  of  grant  assistance  and  information requirements
and  under the  section defining  funding  for restorative  and pre-restorative
activitiy.

Types of Grant Assistance and
Information Requirements for Application

     Perhaps  the  single most significant  deviation  from  the initial program
operating procedure  in the  new  Clean  Lakes  policies  is  the  one which deals
with  pre-implementation  diagnostic-feasibility  studies.    Support  for  pre-
implementation  studies was  specifically  prohibited   in  the  initial  program
guidance  document.  It has become clear that many  States reguire financial  and
technical  assistance  in these endeavors.  The  new regulation authorizes pre-
implementation  studies  to identify and evaluate  lake characteristics  and to
develop a restoration  or  water  guality protection plan as a part of the Clean
Lakes Program.  This  type  of support  is called a  Phase 1  matching grant.  The
Federal government  will  provide  up to $100,000 on a  70% Federal/30% grantee
cost-sharing  basis for Phase 1 grants.  Requirements for the diagnostic-feasi-
bility studies are  included in this paper as Appendix A.

     Actual  implementation  of pollution control measures  or in-lake restora-
tion  methods  and procedures are  to be supported  by  Phase  2 matching grants.
These grants  are the  equivalent of  those  formally issued  under the initial
guidance  document.   The  Federal/state cost-sharing  percentages for  Phase 2
grants  are  proposed  to  remain  at the 50%  Federal/50%   grantee  level.   The
Agency has adopted  the position  that this funding formula will provide suffi-
cient local commitment to assure optimization of project  implementation and a
concern for proper  maintenance  of the  project after it is completed.  Phase 2
grant proposals must contain all  of the information specified in Appendix A to
receive funding  consideration.   This   represents  a significant  tightening of
the requirements for funding  an implementation project.

State Prioritization of Lakes

     Section 314 of the Water Pollution Control  Act Amendments requires States
to  identify and classify  their  lakes  according  to eutrophic conditions.   The
draft regulation  specifies  that  a  State must  accomplish this  by  January 1,
1982,  or  become  ineligible  to  receive Federal funds  under the  Clean  Lakes
Program.   Phase  1  grant funds may  be  used  by States   in order  to comply with
this requirement.  The method of classification and prioritization is left to
the discretion of individual  states.
                                      303

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Application, Review and Evaluation

     Annual appropriations for the Clean Lakes Program have never exceeded $15
million.   The  Office  of Water  Planning and Standards has  taken  the position
that there  is  no  equitable  way to  distribute  such  a  small  amount  of money
among the  States  and  still  maintain a  technically  and  administratively sound
program.   Therefore, the policy will  be to continue  to  review  grant applica-
tions  as  they  are received  and  to  fund  them,  project  by project  based  on
technical  merit.

     Phase 1 and Phase 2 grant applications will  be considered separately, but
both will  be evaluated according to the procedures  outlined in Figure 1  and in
terms of:

     o    Technical feasibility  and the estimated  improvement in  lake water
          quality  as   determined  through  information compiled  by  the  grant
          applicant;

     o    The anticipated positive  changes  in the  overall lake ecosystem with
          regard  to sediment,  nutrient, and pollutant loading  and the  subse-
          quent effects on lake biomass as a result of project implementation;

     o    The degree,   nature  and  sufficiency of unencumbered public access to
          the lake;

     o    The size  of  the  population surrounding the lake which would realize
          recreational benefits  as a result of the project;

     o    Other relatively clean public owned freshwater lakes which may serve
          the same population  adequately;

     o    Whether  the  restoration  project  would  disproportionaly  benefit
          private  land  owners adjacent to  the lake as compared to those some-
          what removed from the shoreline;

     o    The reasonableness of proposal costs in consideration of the various
          proposed  tasks,  likelihood  of  project   success  and the  projected
          benefits;

     o    The  prospect of dealing  satisfactorily  with  adverse environmental
          impacts resulting from the proposed course of action;

     o    The level of state priority for a  particular  grant application; and

     o    The  recommendation  of the review panel members,  including those of
          technical experts  from the university community.

     Within 90 days of the receipt of an application  it will be either funded,
rejected  or returned   to  the  applicant  for  additional   information  or  due to
lack of funds.   In the latter two cases, applications may be resubmitted when
the  issues identified  during  review  have  been  resolved or  when additional
funds become available.
                                      304

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Federal  Funding Restrictions for
Phase 1  and Phase 2 Grants

     Each  State  may apply  for  up to $100,000 in  Phase  1  pre-implementation,
Federal   grant  funds  (on a  70%  Federal/30%  grantee  cost sharing  basis)  to
assist them  in developing complete,  technically sound programs for implement-
ing  lake restorative procedures.  An  application may  address more  than  one
lake.  These funds will  come from the annual Clean Lakes appropriation and may
amount to as much as 20% of that appropriation,  but will  in no event exceed $5
million  per  year.   Each grant will  be  approved  for  a period  not  to  exceed 2
years.

     Further restrictions require  that  the Regional  Administrator will deter-
mine that  pollution  control  measures in the lake watershed have been taken in
accordance with Section 201  (Wastewater Treatment Plant Construction Program),
approved 208 planning (Areawide Waste Treatment Planning Program), and Section
402  (Pollutant  Discharge Permitting Program).  These activities  must be com-
pleted or  progressing according  to the time  schedule of  an approved plan, or
discharge permit schedule, by the time a lake restoration (Phase 2) project is
completed.   Unlike  the  Phase  1  grants,  Phase  2  grants  have no  upper  level
funding  limits.  As per the initial 1976 guidelines,  Clean Lakes funds may not
be used  to  support  projects to control point source  discharges (Section 402)
or for  planning  and construction of wastewater  treatment  facilities (Section
201) where those  programs will  resolve the pollution problems.  Certain other
types of projects  are   similarly  prohibited.  These  include  projects  using
chiefly  palliative   methods  which  treat  symptoms of  pollution  rather  than
attempt  to eliminate  the source  of the problem,  e.g.  harvest of aquatic vege-
tation,   herbicide treatment,  and  maintenance  of lake aeration devices.  Clean
Lakes funds may not be used for desalination procedures  or for the purchase or
long-term leasing of land to provide unencumbered  public access to a lake.

     The  Environmental  Protection  Agency  presently is proposing revised Water
Quality  Management  Regulations  to conform  to the  recently developed extended
management strategy  for  Water Quality  Management,  FY-1979-83.   These regula-
tions set forth  an  increased  emphasis on  State/EPA  Agreements.   The initial
results  of Clean Lakes  Projects  clearly  show  that  this  program can  be  the
basis for effectively implementing  pollution control practices  that improve
dramatically the water quality of both tributary streams and lakes.  State and
local communities  have   shown  a  great  deal  of  interest in  these  results  and
appear impressed with the potential  of this program to assist them with water
quality  improvement.  Thus,  the gradual  development of lake restoration policy
has  served as  an  asset.   It is anticipated that the newly formulated policies
and procedures  of the Clean Lakes Program will  facilitate its implementation.

                                    SUMMARY

     This paper provides  a  statement on the  type  and extent of water quality
     problems associated with freshwater lakes in the United States.

     It  traces the  historical  course of the  Federal  government's involvement
     in water pollution  control activities.
                                      305

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     It explains the  role  of EPA's Office of Water  Planning and Standards in
     administering   the  Clean  Lakes  Program  and the  role  of the  Office  of
     Research and Development  in  evaluating  the effectiveness of various lake
     restoration techniques.

     It describes  the initial  policies  of the  program  and  the  evolution to
     their current  state.

                               ACKNOWLEDGEMENTS

     We wish  to thank Bruce Tichenor, Kenneth  Malueg and  Karen  Randolph of
EPA's  Corvallis  Environmental  Research Laboratory for their  reviews and sug-
gestions  for  improving  this  paper.   A similar  thanks  is extended  to Donald
Porcella,  Associate  Director of  the  Utah State Water Research  Laboratory at
Logan, Utah and  to  Kenneth MacKenthun, Director of  the Criteria and Standards
Division in EPA's Office of Water Planning  and Standards, Washington, D.C.

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Malueg,  K.W.,  et  al.   1973.   The  Shagawa  Lake  Project.   R3-73-026.   USEPA,
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                                  APPENDIX A

GUIDANCE FOR DIAGNOSTIC FEASIBILITY STUDIES

     Proposals  for  Phase  1  Clean  Lakes  grants  must  include  the  following
information in their scope of work for all Clean Lakes applications.

Diagnostic Study Requirements

     1.    An identification of the waters to be restored or studied,  including
          their name,  state in which located,  location within the  state,  area,
          maximum depth,  average  depth,  detention  time, the general  relation-
          ship with associated upstream and downstream waters.

     2.    A geological description  of  the  drainage basin including soil  types
          and soil loss to stream courses that are tributary to the  lake.

     3.    A description of the public access to  the  lake.

     4.    A  summary of historical  lake uses including  recreational  lake uses
          through the present time  and how these  may have changed through the
          years  because  of  water quality  degredation.   A statement must  be
          made  regarding  the water use  of this lake compared to  other  lakes
          within a 50  mile radius.

     5.    An  itemized inventory  of  known point source  domestic or industrial
          pollutional  discharges  affecting or  which  have  affected lake  water
          quality over the past  5  years and  the   abatement  actions  that have
          been taken,  are  in  progress,  or are  contemplated within a specified
          time period.

     6.    A description of  the  land use in the lake watershed with an indica-
          tion of what percentage of the watershed each encumbers.

     7.    A discussion of  non-point pollution  loading derived from each  iden-
          tified land  use category.

     8.    A discussion and  analysis of current (within one year  from the date
          of application) baseline  limnological data.  Such data  must include
          the  present trophic  condition  of  the   water body  as  well as  its
          surface  area,  maximum depth,  average   depth,   hydraulic  residence
          time, area  of the  watershed  draining to the lake, and  the physical,
          chemical,  and  biological impact of   important  tributaries.   Batho-
          metric maps  should be  provided  and  where  dredging is   part of the
          restoration  plan,  representative bottom sediment core   samples  and
          analyses  for nutrient content, heavy metals  and persistent organic
          chemicals  must  be  provided.   An assessment  of nitrogen  and  phos-
          phorus inflows  and outflows  associated with the lake and a hydraulic
          budget including  groundwater flow must  be  included.  Vertical  tem-
          perature  and  dissolved  oxygen  data  are essential  and it must  be
          determined   if the  hypolimnion  becomes anaerobic and if  so,  for how
          long and over what extent of the bottom.   The extent of  algal  blooms
                                      308

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          and the predominent algal  genera  must be discussed.   The portion of
          the shore line and  bottom  that is impacted by vascular plants (sub-
          merged,  floating,  or  emersed  higher  aquatic  vegetation)  must  be
          estimated and that estimation  must  include an identification  of the
          predominant  genera.   There must be  an  identification and discussion
          of major biological resources  in  the lake, such as fish populations
          and how they might be expected to change.

Feasibility Study Requirements

     1.    An  identification  and  discussion  of the  alternatives  for pollution
          control or lake restorative action considered; and an identification
          and justification  of  a selected  alternative when  considering  all
          alternatives  including  a discussion  of  expected water  quality im-
          provement,   technical   feasibility,   and   estimated   costs  that  are
          attached to each alternative.

     2.    A  discussion  of  the particular public benefits  expected to  result
          from implementation of  the  project,  including new public water uses
          that may be associated with the enhanced water  quality.

     3.    A  proposed  monitoring  or  investigative  program with  schedule  for
          evaluation.   Based on the  information  supplied by the applicant and
          the technical  evaluation  of  the  proposal,  a  detailed  monitoring
          program to evaluate project  effectiveness during and up to one year
          following the  completion of  project implementation will  be  estab-
          lished  for each approved project  and will be specified in any grant
          agreements supporting implementation  or  restorative  procedures.   An
          additional  guidance  for monitoring  methods  and  procedures will  be
          provided at the time of grant award.

     4.    A  proposed  milestone work  schedule  for  project completion  with  a
          proposed  budget  and  payment  schedule relating  to  progress  mile-
          stones.

     5.    A  detailed  description   of  how matching  funds  will  be  obtained  to
          support  the  non-federal funding requirements  for the  proposed pro-
          ject.

     6.    A  description of pertinent  relationships  of the proposed project to
          local,  state  and  federal  pollution  control   programs  such  as  the
          Section  201  Construction Grants  Program,  the  Section  208 Areawide
          Wastewater Management  Program, the  Soil  Conservation  Service Pro-
          grams  as described by PL 83-566, the Department of Housing and Urban
          Develooment  Programs, and  any other local, state, and  federal pro-
          grams  which may bear a relationship to the  proposed project.

Environmental Evaluation

     An environmental  evaluation  to  consider  all potential adverse impacts of
the project  must  be  included  with the application.   The purpose of this docu-
ment is to identify and thus minimize the effects of any adverse impacts which
may be associated with the project.


                                      309

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                            SEDIMENTS AND SEDIMENT
                          DISTURBANCE DURING DREDGING
                                John F.  Sustar
                   U.S.  Army Engineer District,  San Francisco
                        San Francisco, California 90105
                                 INTRODUCTION

     During the  past ten years  numerous studies  have been  conducted  in the
field  to  quantify  the  disturbance during  dredging operations.   The  results
have generated wide  ranges  of data.   The conclusions,  however,  do state that
improving the dredging efficiency will  decrease impacts or possible impacts of
dredging operations.  Despite extensive studies in San Francisco Bay,  signifi-
cant chemical  and physical   stresses  on the  biological  communities have not
been identified.   The conclusion on improving dredging efficiency, however, is
still valid in terms of not only minimizing the disturbance to the biological
system, but also  minimizing  the investment in maintaining channels.   Minimiz-
ing disturbance  is  also important where known isolated contamination  is being
removed.

     Studies of  sediment disturbance  during  dredging have  been continuously
modified not only  to locate the disturbance but  to develop handles on ident-
ifying the  parameters that  control  the disturbance.  Figure 1 shows schematic
diagrams of the  three most  common dredging methods  in San Francisco  Bay—the
trailing suction  hopper  dredge,  the  hydraulic cutterhead dredge and the clam-
shell dredge.  The  figure  also  shows  the generally recognized  areas  of dis-
turbance.

     Yagi  et al_.  (1976)  looked at both the hydraulic cutterhead dredge  and the
grab bucket (clamshell)  dredge.   For  the hydraulic cutterhead, they concluded
that:  "The accumulative ratio of short-absorbed soil,  however, decreases with
the increase of the number of cutter  swings.   On the other hand, the turbidity
has the general trend to increase in  opposition to the above mentioned  trend."
Their work  dealt primarily  with  the  swing speed  and  the  sediment thickness.
Shape of bottom was also concluded to  be an important parameter.  The  sediment
type was  only  mentioned  in  terms of  the  gradient of  the vertical  turbidity
distribution.   With  the grab  bucket,  turbidity was  found to  be largely de-
pendent on  the type of  sediment.   The closed bucket, which reduces the inter-
action  of   localized  eddies with  the  sediment interface  in the  bucket,  did
decrease the loading of  the  water column.

     Huston  (1S76)  concluded  that:   "Techniques   for  reducing  dredge-induced
turbidity consist principally  of  good  dredging procedures and  the proper use
of existing dredging equipment.  Some  of the items discussed included  disturb-


                                     311

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ances by  the vessels  themselves  including the  tenders,  the  inefficiency  of
cleanup operations and the effectiveness or skills of the personnel.   His work
did not discuss  the  relationship  of the equipment and the type of sediment in
disturbing both the bottom and the water column,  although proper use of equip-
ment does  imply the selection of  the  type of equipment  for  a given project.
With the  spectrum  of  dredging operations and available equipment, this selec-
tion process  is  not  necessarily  controlled by the  optimization  of the opera-
tion efficiency.

     The work by Weschler et al_.  (1977) does employ a settling jar to evaluate
sediment characteristics  for  use  in a numerical  model.   The mention, however,
does not explain what actually occurs in the system.

     Studies  by  Johnson et  al_.  (1975)  showed  the large  scale  heterogeneous
loading characteristics  of  both  the hopper dredge and the clamshell  with dump
scow.   With  the  operation (elevation changes) of  the  dragheads  on the hopper
dredge, major differences were observed.

     Sustar  et  al_.  (1976)  identified  initial dispersion  patterns related  to
the type  of  sediment  and the dredging  equipment.   The  major portion of their
studies with  the dredging  operation concentrated  on  locating the  plume  and
describing the  plume  vertically  and horizontally  by  percent  transmission  and
suspended  solids  loading.   Although patterns were discernible,  variation  of
data was  very  large.   Studies  were equipment oriented  and project  oriented.

     The type of sediment being dredged has generally been ignored in terms  of
interpreting  the disturbances  that occur  in the dredging  area.  Based  on
previous studies in San Francisco Bay on the release pattern during open water
disposal,  dredging operations  in  the Bay were evaluated  in terms of the type
of  sediment  and the  efficiency  of  the  operation.   An  interpretation  of  the
bottom  and  water  column  disturbance  using  actual  dredging operations  and
sediment testing is given.
                              DREDGING EFFICIENCY

     If  the  basic premise  (increased efficiency decreases  disturbance)  were
reversed, a  greater  disturbance  during the dredging should  reduce  the effic-
iency of  the  operation.   To test this, three  dredging  periods  in Mare Island
using the trailing suction  hopper  dredge HARDING  were evaluated.    Figure  2
shows the location of Mare Island Strait.

     The  shoaling  in  Mare Island Strait  is  silty-clay.   The October-November
1975 dredging  period represented a  shoal formed over  a  several  month period
with sediments  recirculating  in  the  northern portion of  the Bay.   The second
period was  February-March 1976.   The  shoaling generally  represents  new sedi-
ments entering the system with outflows from the Sacramento-San Joaquin Delta.

     The  third  period was  July-August 1978.   Following  an  extended drought,
flood flow  brought new  sediments  from the Delta.  The  delayed  dredging  from
the usual February-March cycle probably developed with progressive movement of
sediments through the Delta and Carquinez Strait with each storm following the
drought.   The total  dredging cycles  for each of the periods were 606, 430 and


                                     313

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            SONOMA
PETALUMA
     , RIVER
            SAN PABLO BAY
                                       BAY 
                       CARQUI  EZ
                       STRAIT \
                                                                 PITTSBURG . ;S

                                                                       SAN JOAQUINRI.
                .';_•" AlARTINE
                 CENTRAL  C.-:. '  ' -
                                                     SCALE IN KILOMETERS
 GOLDENGATE
ปV. OAK LAND
    SAN FRANCISCQ;
                                   ;.:r&" SAN LEANDRO
      -. •  SOUTH'. •'.(
     SAN FRANCISCO^
                        SOUTH  BAY
                                            V.-  > FREMONT
                          REDWOOD CITY .  J • ป.
                                      WLO ALTO.^*]^f>J;^:;. . '.fl.; • • .'
                                INDICATES SUBSYSTEM
                                        BOUNDARIES
                            Figure  2.   Mare  Island Strait.
                                        314

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396, respectively.  Shoaling  patterns  in Mare Island Strait are very definite
with buildups concentrating in three to four areas.

     From the  vessel's records,  the  cubic yards  per pumping  minute  was ob-
tained  for  each cycle  using  the load  meter  and the pumping  time.   The data
were averaged in ten cycle groups to reduce the variability between successive
cycles.  The variability  between cycles results from the heterogeneous nature
of the bottom and variations in dredging location with movement of vessels and
day/night time dredging.  The average efficiency and plus and minus one stand-
ard deviation are shown in Figures 3 through 5.

     All three  periods  show a decrease in  loading  efficiency  with time.  The
first  and second  periods  show definite cycles  of  decreasing efficiency indi-
cating a work  pattern  of removing one shoal at a time.   The type of equipment
(trailing drags)  working  the  shoal  of silty-clay causes both trenching of the
shoal  and  disturbance  with mixing  of  water in the shoal.   After  a  number of
passes through  a  shoal, the dragheads will cross  previous  trenches  resulting
in the intermittent variation of suction at the intake,  increased water in the
slurry  and  subsequent   reduction  in the density of the  pumped sediment.   The
decreased loading  efficiency  of each of the discernible cycles (low ten cycle
average divided by preceding high ten cycle average) is  as follows:

                      Oct-Nov 75             Feb-Mar 76              Jul-Aug 78

1st cycle                72%                    42%                    55%
2nd cycle                59%                    57%
3rd cycle                62%
The  decrease  is  based  on  an  "average  optimum"  condition with  the  initial
dredging of an undisturbed area.

     Although patterns  of decreasing  efficiency  of pumping  are  evident,  the
analysis also  shows some  increases  in  efficiency.   As the  shoals  form with
time, different densities  occur in the bottom.   Assuming optimal  operation of
the  vessel  including  the control  of the dragheads and the speed of the vessel
relative to the bottom,  pumping efficiency is dependent on the density of the
sediment.   As  the  bottom  sediments  are disturbed,  increasing  the water con-
tent, an initial  increase  in pumping efficiency will  occur  until  an  optimum
pumping  density  is  reached.   As  the disturbance continues,  the  density con-
tinues to decrease,  decreasing the pumping efficiency.


                            SEDIMENT RELATIONSHIPS

     Three  types  of sediments were collected in  San  Francisco  Bay to examine
qualitatively  the  comparative  degree  of  disturbance  with  resulting  bottom
configuration  (trenching)  and  suspended particulate.   The  classification of
the  sediments is as follows:
                                     315

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MARE ISLAND DREDGING - HARDING
OCT- NOV 1975 YD3/ MIN VS TIME
AVERAGE 18 CYCLES
HIGH 117 LOW 68
MARE ISLAND DREDGING-HARDING
OCT-NOV 1975 YD3/MIN VS TIME
TWO STANDARD DEVIATIONS 18 CYCLES
MAXIMUM 32  MINIMUM 5
              Figure 3.
                 316

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MARE ISLAND DREDGING- HARDING
FEB - MAR 1976  YD3/ MIN VS TIME
AVERAGE 18 CYCLES
HIGH 92 LOW 39
   i|
MARE ISLAND DREDGING-HARDING
FEB- MAR 1976 YD3/MIN VS TIME
TWO STANDARD DEVIATIONS 18 CYCLES
MAXIMUM 22  MINIMUM 5
               Figure 4.
                  317

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MARE ISLAND DREDGING - HARDING
JUL-AUG 1978 YD3/ MIN VS TIME
AVERAGE 18 CYCLES
HIGH 113  LOW 59
        l|
MARE  ISLAND DREDGING - HARDING
JUL-AUG 1978 YD3/ MIN VS TIME
TWO STANDARD DEVIATIONS 18 CYCLES
MAXIMUM 26  MINIMUM 6
               Figure 5.
                 318

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      Classification

 1.   Silty Sand (SM)
 2.   Sand (SP)
 3.   Clay (CH)
                                  Liquid
                                  Limit

                                  31

                                  99
Plastic
 Limit

 26

 38
 5

61
 The gradation curves are shown in Figure  6.
  100
CO
01
UJ
50
bJ
CJ
o:
LJ
CL
                                        11Vf VTVT	
                         111 i  i  I  I   I
      10
       Figure  6.
                      I                O.I              0.01
                      GRAIN SIZE IN MILLIMETERS
                   0.001
      The  sediments  were placed  in  clear 30  cm  x  16 cm containers with nine
  centimeters of salt water over the sediments.   A  standard disturbance was made
  in  each container using a  nine  millimeter  diameter  rod.   The rod was pulled
  along  the  same  line  in groups of five pulls.   Uniform  speed and pressure were
  maintained.

      The  clay,  sample  3,  produced the best defined trench with vertical side
  walls.   The  width of  the  trench (15  cm)  was not significantly changed with
  increased  disturbances  along the same  line.   The  silty sand, sample 1, also
  developed  a trench.   Vertical walls  were present,  but were  not as well defined
  as  with the  clay.   The width of  the  trench  (25  cm)  increased with increasing
  disturbance.   The  sand, sample  2,  developed  a V-shaped trench,  30 cm at the
  top.
                                     319

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     Sand produced very little turbidity when comparing the suspended particu-
late to  a photo  density  scale  (visual  observation).   The  silty  sand almost
immediately  produced  turbidity  with  very  little  increase in  turbidity  with
additional disturbance.   The clay  produced successive increase  in turbidity
with each  additional  disturbance.  The  maximum turbidity  with the  clay  was
greater than with the silty sand.

     The differences  in the  trenches  can be explained by the type of sediment
irrespective  of  the type  of disturbance.    Following  a disturbance  the  sand
comes to  an  angle of repose, resulting  in  a V-shaped trench.   The silty sand
maintains  some  vertical  wall  because  it  is  a  low cohesive  sediment.   The
increased width of  the  trench  results from the susceptibility of the sediment
to  erode  with  successive disturbances.   As  the  cohesive properties  of  the
sediment  increase,  the  direct  action  by the disturbing instrument is required
to  move  the  sediment.  The  narrow width  of the  clay  trench  is  an example.

     Within San Francisco  Bay,  the type of sediment does influence the pumping
efficiency when  comparing Mare  Island  Strait  (clay),  Richmond Harbor (silt)
and the San Francisco Bay  (fine sand).  Mare Island Strait sediment is conduc-
ive to the  most  efficient pumping.   The San Francisco Bar sediment results in
the least pumping efficiency.  Pumping efficiency is defined by cubic yards of
load per pumping minute.

     In Mare  Island  Strait,  the  sediments are less susceptible to mixing with
water;  that  is,  more  energy  or disturbance  is  required to decrease the dens-
ity.  It  should  be  noted  that efforts are  made  to control the dredging lines
(i.e.,  reduce the  crossing of  trenches).  Dredging cycles have been conducted
in  Mare  Island  Strait with a hopper  dredge  in which no overflow was required
to  attain  an  economic load.   This means that  the  sediments were near optimum
pumping density and excellent control  of dredging lines was maintained.

     The  silts in  Richmond Harbor are easily  disturbed,  resulting  in a sedi-
ment density  below the optimum  pumping  density.   The  sands on  the San Fran-
cisco  Bar are  independent  of  the disturbance.   The  pumping  efficiency  is
controlled by the  efficiency of  the pumps  rather  than  the disturbance of the
sediment.    The  speed  of   the  dredge  over  the  bottom  largely  influences  the
loading characterization.

     The same dredging  operations  in  San Francisco  Bay illustrate  the levels
of  suspended  particulates during dredging.  Greater  turbidity (reduced light
transmission) results from clays  because of the increased number of particles
in  suspension per  unit  weight  as compared with silts.   The  level  of  clay
loading (weight suspended solids)  is  dependent on the duration of disturbance
(addition  and mixing of  water  to  decrease  the cohesive  properties)  and  the
flocculation rate.  The flocculation rate is dependent on the concentration of
suspended solids, salinity of  the system and collision of particles (disturb-
ance in the  operation,  i.e., overflow,  and in the water column, i.e., passage
of  the  vessel).   With  Mare  Island Strait  sediments,  the  non-dispersed grain
size is about 20 micron.  Without additional disturbance,  the clays within the
hydraulic regime  will  react  as  silts.  Although the level  of suspended solids
in  the water  column between  clays and silts may be similar, percent transmis-
sion will  be dramatically different.   Figure 7 represents  a  logarithmic  re-
gression  analysis  of seven  sets  of  data.   The data present  i_n situ percent


                                     320

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transmission readings,  using  a ten  centimeter  light  pattern,  compared with
suspended solids analysis of samples pumped from adjacent to  the  transmissom-
eter.   The analysis does fit the above description.   The  clays  of Mare  Island
Strait generate the highest turbidity (decreased light transmission) as com-
pared to the coarser  silts  in other areas such as Richmond Harbor and Alameda
Naval  Air Station.   Within the three regression curves of Mare  Island Strait,
the lowest of the  curves  is at a time of lower salinity with  freshwater flows
coming from the Sacramento-San Joaquin Delta.   The  lower  salinity of both the
sediment and the water decreases  the rate of flocculation and increases the
time of sediments in suspension.  Dredging with stratified water conditions in
Mare  Island  Strait  introduced  saline water from the  lower water column into
the freshwater  in  the upper water  column.   The results  were  a  decrease  in
turbidity in the upper water column due to flocculation.
                  50           100           150          200
                    SUSPENDED  SOLIDS IN MILLIGRAMS  PER LITER
                                                                   250
Line

 A.
 B.
 C.
 D.
 E.
 F.
 G.
Location
Date
(f)x
Mare Island Strait
Mare Island Strait
Mare Island Strait
Alameda NAS
Alameda NAS
Richmond Harbor
Petaluma Channel
Sep-Oct 74
Mar
Oct
Dec
Jan
Nov
Sep
75
75
74
75
74
77
104
24
30
38
99
83
268
55
7
46
120.
117.
135.
114.
.91-9.
.87-1.
.33-8.
59-15.
09-20.
17-21.
66-18.
22
41
30
58
66
22
68
1 nx
Inx
1 nx
1 nx
1 nx
1 nx
Inx
0.
0.
0.
0.
0.
0.
0.
56
46
54
,26
.42
.35
75
(1)  f(x) = ฐ,
(2)  Samples
(3)  Samples
     '< transmission  10  cm  light path.
     greater than 500  mg/1  suspended solids excluded.
     0% transmission entered at 0.01%.

                           Figure 7.
                                     321

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     The turbidity  associated  with  sand  is  limited to the percent  silts  and
clays in the  sediment  and the  type and size  of  equipment.   The type and size
of equipment  relates  to  the disturbances  and the absorption ratio.   The  ab-
sorption ratio is the  ratio of  sediment removed divided by sediment disturbed.
The  hopper  dredge, working with  sand,  does  introduce  grading  of  sediments
during dredging.   Fines are separated through the overflow.   The reduced fines
level in the hopper does result in lower turbidity during disposal.   This also
is reflected  in  the contaminant  levels.   Contaminants in the  disposed sedi-
ments are less than the in situ project sediments.   A large clamshell dredge
will   maintain a  greater percentage  of fines  for transport.   The  turbidity
during  disposal,  however, will be  greater than from  a  hopper  dredge because
the  fines are  still present.   The turbidity  from  a  hydraulic cutterhead will
depend  on the  ratio of absorbed sediments, which  in  turn relates to the suc-
tion's  pickup  capacity,  swing  speed,  working face and type  of  sediment.  The
four elements are interdependent.
                                  CONCLUSIONS

     The  type  of sediment  being  dredged is  a  major  parameter  in evaluating
both  the disturbance  generated by  the  operation and  the efficiency  of  the
operation.  The  disturbance and  the efficiency are related.  With  silts  and
clays a  less  efficient operation  means that more  energy  is  being expended in
adding and mixing water with the  sediment.   As  the disturbance increases,  the
efficiency continues to decrease.

     Many studies have been conducted during the past several years to define
the  disturbance  during dredging.    The great variation of results within  and
between  studies  probably  could be  correlated  if the  type  of  sediment,  the
shape and condition  of the shoal, the type of equipment,  the method of opera-
tion and relative time of sampling were entered  into the analysis.  The liquid
limit and  water content  (presented  as multiples of the  liquid  limit)  of  the
sediments at any particular time and location of the operation are proposed as
a common  basis  for  evaluating levels of suspended solids  in  the water column.

     Continuous  "optimum"  efficiency  of  a  dredging operation can not  be  ex-
pected.   Other constraints override the optimum  conditions, such as the avail-
ability  of  a  particular type  and size  of  dredge,  requirements  to  minimize
interruptions of commerce, localized channel  requirements  and safety.   Some of
the  factors can  be  controlled or  developed to increase or maintain the effic-
iency of  the  operation.   Training operating personnel  to  become familiar with
the  equipment  in various  types of sediments and shoal  configurations is prob-
ably  the  most  effective.   Use of   instrumentation  for  horizontal  and vertical
control   will  also increase  efficiency.   With  hydraulic  systems  such  as  the
hopper  dredge  and the  cutterhead  dredges,  recently  developed instrumentation
should  be  utilized   to  indicate immediate pumping response  to both increases
and  decreases in pumping densities.  Clogging of pumps or  breakage of sediment
suction will  be  reduced and a more "optimum" density will be maintained.   The
design  of the dredging  operation should minimize feather shoals and cleanup
requirements.   This  may mean an evaluation of  neat  line  payment  schedules in
favor of some combination of neat line and pumpage quantities.
                                     322

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                                ACKNOWLEDGEMENT

     The material in  this  paper is based on  the  author's  observations during
studies by the  San  Francisco District of the U.S.  Army Corps of Engineers of
dredged sediment disposal in San Francisco Bay.   Publication of this paper has
been approved by  the  Corps of Engineers.  Any  views,  interpretations  or con-
clusions developed,  however, are those of the writer.

     Critical comments  by  Mr.  William  Dickson  of the  District's  Operations
Division is  appreciated.   Special  thanks is extended to my two oldest child-
ren, Peter and  Mary,  who have reached the age of a scientific appreciation to
play with  mud.   Their  assistance  in mixing the mud, making observations and
measurements  and cleaning up afterwards was a great help.


                                  REFERENCES

 1.   Huston,  J.  W.,  W. C. Huston, Techniques for Reducing Turbidity Associated
     with Present Dredging  Procedures  and Operations, Contract Report D-76-4,
     U.S.  Army Engineers Waterways Experiment Station, Vicksburg, Mississippi,
     May 1976.

  2. Huston,   J. ,  Techniques  for  Reducing  Turbidity  with  Present  Dredging
     Procedures  and  Operations,  Proceeding World, WODCON  VII,  San Francisco,
     July 1976.

 3.   Johnson, E. , et  al. ,  JBF Scientific Corporation published  as  (U.S.  Army
     Engineer District)  Dredge  Disposal  Study,  San Francisco Bay and Estuary,
     Appendix M, Dredging Technology, San Francisco, September 1975.

 4.   Sustar,' J.  F.,  T. H. Wakeman and R.  M.  Ecker,  "Sediment-Water Interaction
     During  Dredging  Operation," Proceedings of ASCE Specialty Conference on
     Dredging and Its Environmental  Effects, Mobile, AL,  p.  736-767,  January
     26-28, 1976.

 5.   Sustar,   J.  F. ,  G.  Perry,  T.  H.  Wakeman,  "Sediment Dispersion  from  a
     Submerged  Pipeline,"   Proceeding  Coastal   Zone  78, San  Francisco,  14-16
     March 1978.

 6.   U.S.  Army Engineer District, Dredge Disposal Study, San Francisco Bay and
     Estuary, Main Report,  San Francisco, CA, April 1976.

 7.   U.S.  Army Engineer District, Dredge Disposal Study, San Francisco Bay and
     Estuary, Appendix  A,  Main Ship  Channel,   San  Francisco,  CA,  September
     1975.

 8.   U.S.  Army Engineer District, Dredge Disposal Study, San Francisco Bay and
     Estuary, Appendix C, Water Column, San Francisco, April 1976.

 9.   Wakeman, T.  H.  ,  J.  F.  Sustar and W. J.  Dickson.   1975.  Impacts of Three
     Dredge  Types Compared  in  San  Francisco  District.   World  Dredging and
     Marine Construction 11:9-14.
                                     323

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10.   Weschler,  B.  A.,  D.  R.  Cogley,  A  Laboratory  Study  of  the  Turbidity Gener-
     ation  Potential  of Sediments  to be Dredged,  Technical  Report  D-77-14,
     U.S. Army  Engineers  Waterways  Experiment  Station,  Vicksburg,  Mississippi,
     November  1977.

II.   Yagi,  T. ,  T.  Koina, S.  Miyazaki,  Turbidity  Caused by Bay  Dredging,  Pro-
     ceeding  World Dredging Conference, WODCON VII,  San Francisco,  July 1976.
                                     324

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             BIOACCUMULATION OF TOXIC SUBSTANCES FROM CONTAMINATED
                    SEDIMENTS BY FISH AND BENTHIC ORGANISMS

                               Robert M.  Engler
                           Environmental  Laboratory
                       Dredged Material  Research Program
                U.S.  Army Engineer Waterways Experiment Station
                         Vicksburg, Mississippi  39180
                                  BACKGROUND

     The River and Harbor Act of 1970 (Public Law 91-611, Section 123) author-
ized the Corps of Engineers to initiate and conduct a comprehensive nationwide
study  of  dredging  and dredged  material  disposal  operations.   Of  particular
interest were environmental  impacts,  productive uses of dredged material, and
new and/or improved dredging and disposal practices.

     The  U.S.  Army  Engineer  Waterways  Experiment Station  (WES)  was  assigned
responsibility for  the research  program;  the  program  was  designated  as the
Dredged Material  Research Program (DMRP).

     The planning and implementation of the DMRP were the responsibility of an
interdisciplinary team established at WES as part of the Environmental Labora-
tory  (EL).   The  thrust of  the program involved four major research  projects
(1):

     a)   Environmental Impacts and  Criteria Development Project (EICDP).

     b)   Habitat Development Project.

     c)   Disposal Operations Project.

     d)   Productive Uses  Project.

     This review report is primarily concerned with the findings from Task ID,
the Effects  of Dredging  and Disposal on Aquatic Organisms, and from Task 1A,
the Aquatic Disposal  Field Investigations (ADFI), of the DMRP and observations
from  two  of the  five  open-water disposal  sites.  Findings from related work
will be referenced in this review as  appropriate.

     The overall   objective  of the EICDP was to provide definitive information
on  the  environmental   impact  of dredging and  disposal  operations  and,  where
undesirable impacts  were observed, to suggest means of eliminating or reducing
such  impacts.   As  such,  this  also  included  studies  on   water  and  sediment
quality and  the   rate  and  extent of  the recolonization of disposal  sites by
                                      325

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bottom  organisms,   impacts  such  as  bioaccumulation  of  toxic  substances  on
bottom  animals,  and  responses  of  swimming  and  free-floating organisms  to
disposal.

     Task ID  (2) included  six research efforts that dealt with  the direct and
indirect effects of dredging  and disposal on  aquatic  organisms.   The aspects
of dredging and disposal investigated for potential environmental  effects were
the physical disruption of the bottom environment,  the generation  of suspended
sediments,   and  the  contaminant load  of  the  sediments  being  disturbed  and
redistributed.

     The research  reviewed  is in the forefront of  applied  environmental sci-
ence and is  a beginning in defining the occurrence of environmental perturba-
tions due  to dredging  and  disposal.  Most of the studies  reviewed describe
worst-case  experimental  conditions.   Although  somewhat   limited   in  scope,
experimental laboratory results showing lack of effects under these conditions
support  the conclusion  of the  field  studies that  indirect  (long-term  and
sublethal) effects  of dredging and disposal will be  minimal.

     Potential environmental  effects  of  dredging  and  disposal  are  not  yet
completely  understood due to  the many variables involved.  Dredging and dispo-
sal operations are  carried  out in many geographic  locations with  a wide range
of  aquatic  environments.   Waters  may  have  different  salinity  regimes  and
different  levels  of  natural  turbidity.   Disturbed  areas  may  have different
contaminant  burdens in  the  water   and  sediments.   Major  variables  are  the
presence of  organisms  and  the species diversity that characterize the differ-
ent  dredging and  disposal sites.   Even  different  methods  of dredging  and
disposal may affect the environmental impact of  a given project.

     The basic approach  involved the selection of  field sites on  the basis of
representativeness  of different geographic regions  (environments)  and disposal
operations.   Appropriate strategies were then  developed for the  collection and
analysis  of biological,  chemical,   and  physical  samples.   Samples  were then
taken during  controlled disposal operations and compared  to  samples obtained
under baseline conditions and  from reference sites.

FIELD STUDY RESEARCH SITES

Lake Erie (Ashtabula,  Ohio)

     Seasonal aspects of  spring and summer hopper  dredge disposal  of contami-
nated and uncontaminated  sediments  from Ashtabula  Harbor were investigated at
this site.   In  addition, the long-term  impacts at  a  historic disposal site
were evaluated.  This was the only site located entirely in freshwater.

Duwamish Waterway (Puget Sound, Washington)

     This site was  chosen  for investigations  of the  disposal of  contaminated
sediments in an estuary.  Fine-grained sediments contaminated with polychlori-
nated biphenyls  (PCBs), metals  and petroleum hydrocarbons  were  mechanically
dredged  from  the  waterway, barged  to an Elliott Bay  (Puget  Sound) site,  and
disposed of in 60 m of water.
                                       326

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RtStARCH RATIONALE

     In  general,  a multidiscipl inary  team  approach was used at  each  site to
investigate the  effects  of dredged material  disposal  (3).   The  primary vari-
ables studied  were physical, chemical, and biological parameters as follows:

     Physical:  Currents, waves, tides, meteorology, bottom profiles, sediment
     movement, sedimentology,  geochemistry,  and mineralogy.

     Chemical:  Water quality, sediment quality, toxicant release/removal, and
     nutrient release/removal.

     Biological:    Fish,  shellfish,  benthic  macroinvertebrates,  phytoplankton,
     zooplankton, contaminant  bioaccmulation,  and recolonization.

Not all  variables were investigated at each  site,  however,  this review deals
only  with the  contaminant uptake  potential for  select toxic  substances by
aquatic organisms.

     Three other  task  areas within the EICDP (1) were closely related to this
work.   These were:  Movements  of Dredged Material (Task IB), Effects of Dredg-
ing  and  Disposal  on  Water  Quality  (Task  1C), and  Effects of  Dredging and
Disposal  on  Aquatic Organisms  (Task ID).  The research for  these  tasks was,
for the  most  part, carried out in the laboratory under controlled conditions.
As such,  the  results  are useful for  understanding  known  impacts and for pre-
dicting  others that  may  occur.   They cannot, however,  be  directly  applied to
field  conditions  without verification  but  can be  considered as  "worst case"
evaluations.    As  such,  they  are  useful  in defining boundary conditions ex-
pected with aquatic discharge.

     Results obtained  in the field studies  may be site-specific.   Dredging and
disposal  will  almost  always  cause  some  degree of  environmental  disruption.
Disposal, for  example,  will usually cause the burial  of organisms.

     The  apparent  absence  of  an impact does not definitively demonstrate that
one did  not occur.  Rather,  it may reflect a  deficiency  in  experimental de-
sign,  inappropriate methods,  or analytical  error.   This is a particular prob-
lem in  the  case  of chronic or  long-term  impacts  because these  may not become
evident for months or years after the causal  event.


                           LABORATORY INVESTIGATIONS

     Dredging  and disposal  are carried out  in  different  locations  throughout
the United States and  in the  territorial sea.  Very often disposal  is carried
out in an environment  different from the dredging site.  Dredging and disposal
occur  in waters  ranging from  fresh to  estuarine  and high  salinity  waters.
Some  of  these  waters  are  highly  turbid,  whereas  others  normally  are  quite
clear.   Different dredging areas  may  have different contaminant  burdens in
waters and sediments.  Another major variable is the organisms present and the
species  diversity in  different dredging  and  disposal  areas.    Some  benthic
substrates may  host hundreds  of  species  within areas of a  few  square meters
                                      327

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while other substrates  may  host very few species.   1 he  presence  of  many dif-
ferent  species  at a  given  location has  been classically  interpreted  as the
sign of a  healthy ecosystem.   This  is  not always true, and it is  important to
also take  into  account  the  number of major different types of organisms.  For
example,  in  the  Oakland  Inner Harbor  of  San Francisco  Bay,  there  is  great
animal  diversity, but most  of the different  species are sludge  worms,  with a
number of  other  species which are diminuitive,  opportunistic, and  adapted to
pollutant  stress.   Conversely,  potentially  damaged species may bp  of commer-
cial  value,   i.e.,  the  east  coast  oyster  beds.   Local pollutant  additions
unrelated  to  dredging  may  exceed potential dredging  and  disposal  effects or
may act synergistically with  dredging  and disposal to  produce deleterious or
beneficial  environmental  effects.   Even different  methods  of  dredging  and
disposal may affect the  environmental impact  of any  given project.

     Previous   literature  on  dredging  and  disposal  has been fragmentary and
site or  resource specific.    Reviews  of literature reveal  that too  few basic
data form  a broad  scale  conceptual framework for the possible  environmental
impacts.

CHFMICAL IMPACTS

     The potential availability and uptake of sediment-associated  heavy metals
by deposit-feeding benthic animals was  the subject of DMRP Work  Unit 1D06 (4).
This laboratory  study  attempted  to  determine the biological availability of
selected  heavy  metals  associated with  sediments and  the  potential  for their
uptake  from dredged  material  into the tissues of representative  bottom-dwell-
ing species.

     Sediment chemistry in relation to organisms  impact was further studied in
Work  Unit 1D11  (5).    This  study carried  out  laboratory  experiments  on the
transfer of oil  and  grease  residues from oil-contaminated  sediments  into the
tissues of some  representative benthic species.

     There has  been  concern that contaminants from municipal, industrial, and
other sources which  become  entrapped in aquatic  sediments may become biologi-
cally active  when disturbed by dredging or disposal  activities.   Major mater-
ials in question  have been  numerous heavy  metals, persistent pesticides such
as  DDT  and its  derivatives,  PCBs  and  petroleum  hydrocarbons.    Dredging and
disposal do not  introduce new contaminants  to the aquatic environment,  but at
worst simply  redistribute  the  sediments  which  are the  natural  depository of
contaminants introduced  from other sources.

Toxic Substance Uptake

     In Work  Unit 1D06  (4), metal availability  and  accumulation  studies were
conducted  using  the  clam Rangia cuneata, the grass shrimps Palaemonetes pugio
and  P.  kadiakensis,   and  the  worms  Neanthes  arenaceodentata and  Tubifex sp.
Test sediments,  as shown  in  Table  1,  were taken from  Texas City and  Corpus
Christi, Texas,  ship  channels (15 and 30 ฐ/0o salinity, respectively) and the
Ashtabula  River  in Ohio  (freshwater).   Metals  routinely  measured were iron,
manganese, copper, cadmium,  nickel, lead, zinc, chromium, and mercury.
                                     328

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             TABLE 1.   "I01AL CONCENTRATION OF METALS IN SEDIMENTS




Element
Cu
Cr
Cd
Fe
Ni
Mn
Pb
Zn
Hg
V
Total Concentration,
Texas
City
Channel
48
188
2.4
14,500
48
570
41
161
0.6
136
mg/kg of Dry Weight
Corpus
Christi
Channel
120
82
21
12,000
17
257
316
4,055
18



Ashtabula
River
37
175
4.8
25,000
52
356
42
315
1.1
222
                            Elutriate Test Results


Metal
Cu
Zn
Mn
Fe
Pb
Cr
Cd
Ni
Hg
Texas
Site water
((jg/1 )
20
44
32
44
1
7
<1
85
0.05
City
El utriate
(M9/D
9
28
5800
52
1
6
<1
75
0.10
Corpus
Site water
(ug/n
9
325
22
10
2
<5
<]
11
<0.05
Christi
Elutriate
(ug/1)
3
1700
890
20
6
<5
<1
9
0.55
Ashtabul
Site water El
(ug/1)
8
85
3
15
1
<5
<]
21
0.11
a
utriate
(ug/i)
6
50
550
650
1.5
<5
<1
20
2.85

     For most  metals  studied  (Table  2)  uptake by organisms was  not evident.
However, when  uptake was  shown to occur,  the levels  often varied  from  one
sample period  to  another  and were quantitatively marginal, usually being less
than one order  of magnitude greater than levels in the control  organisms even
after 1 month  of  exposure.   It is invalid to  compare  metals levels in organ-
isms to total sediment chemical concentrations since only a variable and small
amount of  the  sediment-associated metal  is  biologically  available.   This  is
discussed in detail  in  the synthesis  report on DMRP Task  IE (6).   In addition
to not knowing the amount of metal available  for biological uptake, animals  in
undisturbed environments may naturally have high and fluctuating metal levels.
Therefore,  comparisons  should  be  made between control  and experimental organ-
isms at the same point in time in order to evaluate bioaccumulation.
                                      329

-------











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     Of  a total  of  168  animal-sediment-sal irn'ty  combinations  evaluated  in
tests carried out by Neff, Foster, and Slowey (4), only 22 percent showed sig-
nificant  accumulation  due to  sediment exposure.  The  largest uptake  was  of
iron,  a  metal  generally  known  for  its  low degree  of  toxicity  in biological
systems.   Significant  accumulations  of lead  were seen in a  number  of short-
term exposures, although these could not be duplicated in long-term exposures.
Relatively high  uptake of  lead  occurred  only in the  polychaete  Neanthes and
was  interpreted  to  be  potentially ecologically  significant  for  this species.
Their  literature search showed that heavy metals in solution vary over several
orders of magnitude in availability to benthic  invertebrates.   Although ac-
cumulation of  heavy metals  by  organisms  from the water  has  been  documented,
the  literature  shows no  such  clear evidence for accumulation of  metals from
the sediments.

     Neff, Foster  and  Slowey  (4) also investigated  the depuration  of heavy
metals after the  organisms  were  removed from the test sediments.  In those 37
cases  where  there was  uptake after 8  days  exposure,  depuration  during 2 or 8
days in  clean  water was seen in  7  instances,  with the other 30 cases showing
no decrease in  metal  concentration in the tissues.

     In  a field investigation of the San  Francisco Bay  system,  Anderlini  e_t
al_.  (7)  looked  at  9 heavy metals  (silver,  arsenic,  cadmium,  copper, mercury,
nickel,  lead,  selenium,  and zinc)  and  5  invertebrates  (Ampelisca mi 1leri,
Hacoma balthica,  Neanthes succinea, Mytilus edulis,  and Ischadi urn demissum).
Metals concentration in sediments and organisms fluctuated within and outside
the  dredged  zone during  the period of the study.  Changes  in the mean metal
concentrations in sediments  and all invertebrates during the study period were
relatively small, considerably  less than one order  of magnitude.   Mean metal
concentrations in sediments  and  benthic invertebrates changed by  less than a
factor of  2,  and changes  in metal  levels  in  M.  edul i s were no greater than a
factor  of 3.   These changes  could  not  be  directly  attributed  to dredging
activities.  Metal  concentrations  were  similar  in M. edulis which were trans-
planted  from clean  water to  stations within and  outside the  dredged zone.
Mussels  transplanted to contaminated Bay  stations appeared to accumulate cop-
per, nickel, and  zinc  over  controls kept in  clean  water coastal stations but
to  a  lesser  extent  than native mussels.  Desorption of  metal  species by mus-
sels 27  days after  being  transferred  from  Bay or ocean  stations  occurred  in
the  following  order of decreasing depuration:   zinc > mercury >  copper > lead
>  nickel  > cadmium  > arsenic.   Selenium was not  depurated from  mussel tissue
in 27 days.

     The  accumulation  potential  of a metal  may be affected by several factors
such as  duration of exposure,  salinity,  water  hardness,  exposure concentra-
tion,  temperature,   and  the particular  organism  under  study.  The relative
importance of these  factors  varies from metal to metal.  Data of Neff, Foster,
and  Slowey  (4) on  salinity  effects are  inconclusive, but there  was a trend
toward  increased uptake  at  lower salinities.   Anderlini  et a_]_. ' s  (7) 9-day
laboratory study exposed  M.  balthica to the chloride  salts  of various metals
in  the  water  column.   These data  support  field  observations  in   which  M.
balthica  showed  the highest metal  concentrations following  dredging periods
where heavy rains had resulted in a marked decrease in salinity.
                                      331

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     The Neff, hoster,  and  Slowey (4) study indicated  that  the  chemical form
of metals had important effects on their bioavailabi1ity.  Elevated concentra-
tions  of  heavy  metals in  tissues  of benthic  invertebrates were  not  always
indicative of high  levels  of metals in the ambient medium or associated sedi-
ments.   Although a few instances of uptake were seen to be of possible ecolog-
ical  significance, diversity of results among species,  different  metals, types
of exposure,  and  salinity  regimes strongly argued that bulk analysis of sedi-
ments for metal  content could not, be used as a reliable index of metal  avail-
ability and  potential ecological impact of dredged  material.

     Neff, Foster, and Slowey (4) performed sequential  and nonsequential chem-
ical  extractions on the sediments to evaluate the  potential  mobility of metals
in different  chemical  forms.   They  also  determined the total metal concentra-
tion in the sediment.  For some species a correlation did exist and for others
a correlation did  not  exist between any chemical  or physical form studied and
bioaccumulation of  the  metal.   These  authors state:  "At present, it does not
appear  that  a simple  extraction  scheme  can be developed that might indicate
availability  of sediment sorbed metals by benthic organisms.   Additional data,
based upon  a  large  number of different sediment types, may indicate, however,
forms most likely to be accumulated by benthic organisms."

     For some metals  there  appears  to be good  correlation  between metal con-
centration in the sediment and in the associated infaunal and epifaunal  macro-
biota  (4).   For  other metals no  such  correlation exists.   These correlations
often vary with sediment type.  The correlation, when it occurs,  may be due to
direct  or indirect  transfer of metals from sediment to biota or  it may repre-
sent the presence of a common source of metals to  both the sediment and biota.
Anderlini et aJL  (7) concluded that if changes in  metals in the water occurred
as a  result  of  dredging  activities,  the changes  were  either  less than small
natural fluctuations or were of short duration.

     Both Neff, Foster, and Slowey (4) (short-term laboratory studies and lit-
erature review)  and  Anderlini  e_t al.   (7) (longer term field work and back-up
laboratory  experiments)  have  found   the  same heavy  metal   phenomenon.   The
accumulation and release of certain heavy metals seems to vary with the metal,
with the  species,  between  sampling times, between sampling sites  (dredged and
not dredged), and  within  controls.   These variable results  have  not been di-
rectly correlated with  dredging operations or sediment loading.

     A  recent field  study  supporting the laboratory results  of  Neff, Foster,
and Slowey  (4)  has  been carried  out  by  Simms  and Presley (8).  These authors
concluded that  mollusks,  crustaceans,  and  bony  fishes  from dredged areas of
San  Antonio  Bay were  lower in  almost every heavy metal  than were organisms
from other  areas  where dredging was minimal.  Mollusks  were  observed to con-
centrate metals more than any other organisms studied,  but the levels observed
were much  lower than those  thought  to be lethal  or toxic.   Except  for a few
large fish,  metal  concentrations  did not correlate significantly with size or
growth  stage.  Vigorous shell  dredging in the Bay for 50 years apparently did
not cause increases  of heavy metals in the tissues  of local biota.

     Studies  in  DMRP  Work  Unit  1D09  (9)   used  harbor sediments  chosen for
physical similarity  to  bentonite, in order to assay for impacts  due to chemi-
                                      332

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cal properties of  the  sediments in suspension.  Measurements were carried out
using  sediments  from relatively  uncontaminated  reaches of  San  Francisco Bay
and  compared  with  measurements on  more  highly  contaminated Bay  sediments.
Organism  responses did  not  differ greatly  between pure  mineral  suspensions
(10) and uncontaminated natural sediments.  In many cases,  lethal effects were
more marked  with  the  contaminated  sediments.  Sediment  characteristics are
presented in Table 3.  The most sensitive species tested, striped bass, Morone
saxati 1 is,  survived  only  a  few hours  at levels of  0.5 g/1  of contaminated
sediments, a condition  probably representing a worst-case of turbidity genera-
tion associated with a  dredging operation.  Such conditions are very unlikely
to occur in the field,  where motile organisms may escape turbidity maxima, and
where water currents disperse  sediments as they settle  out  of the water col-
umn.

     Chemical   analyses  of several  species for heavy  metals,  pesticides, and
polychlorinated biphenyls  (PCBs)  as  presented in Tables 4-7, indicated uptake
of several contaminants,  but none were accumulated to levels which appeared to
be  sufficient  to  influence the survival  of the exposed organisms (9).  Diffi-
culties  in  interpreting  such chemical  data argued for developing assays which
evaluate total  toxicity of  a sediment regardless of specific toxicants.

Oil and Grease Uptake

     This term is  used  collectively in describing all components of sediments
of  natural and contaminant origin which  are  primarily  fat soluble.   The lit-
erature  review contained  in DMRP  Work Unit  1D11  (11) demonstrated  a broad
variety  of  possible oil  and grease components  in  sediment,  the recovery of
which  was  dependent on  the  type  of  solvent  and methodology  used  to extract
these  residues.  Trace contaminants,  such as  the PCBs  and chlorinated hydro-
carbons  (DDT  and  derivatives), often  occur  in  the  oil  and  grease.   Large
amounts of contaminant oil and grease find their way into the sediments of the
Nation's waterways either by  spillage  or as  chronic  inputs  in  municipal and
industrial effluents, particularly near urban areas with major waste outfalls.
The  literature  suggested  long-term  retention of oil  and  grease  residues  in
sediments with  minor biodegradation occurring.  Where  oily  residues of known
toxicity  became  associated  with  sediments,   these  sediments retained toxic
properties  over  periods  of years  affecting  local  biota.  Spilled  oils are
known  to readily  become  adsorbed to  naturally  occurring  suspended particu-
lates,   and  oily  residues  in municipal  and  industrial  effluents are commonly
found  adsorbed to  particles.   These  particulates  are  deposited  in benthic
sediments and  are subject to resuspension during disposal.

     Using the elutriate test DiSalvo e_t aj.  (11) showed some release into the
water of  soluble  hydrocarbon residues  from sediments known to contain 2000 to
6000 ppm total hydrocarbons.  Hydrocarbon concentrations in the elutriate (100
to  400  ppb) were  from 11  to  400  times  higher than background,  yet  were well
below  acceptable   effluent  discharge, standards.   The  amount of  oil  released
during the elutriate test  is less than 0.01 percent of the sediment-associated
hydrocarbons under worst-case conditions.

     A  test  scheme  was  employed  in  which  estuarine  crabs  (Hemigrapsus
oregonensij),   mussels  (Mytilus edulis),  a"d  snails  (Acanthina  spirata), and
                                       333

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TABLE 3.   CHEMICAL CHARACTERIZATION OF CONTAMINATED SEDIMENT
          USED IN THE ESTUARINE AND MARINE TESTS

Parameter
% water
pH
Eh
Total
Sulfides
Total
Phosphates
Ortho-P
TKN
HNj-N
As
Cd
Cu
Fe
Mn
Hg
Ni
Se
Zn
Total
PCBs
Total DDT

Total
mg/kg
48.3
7.8
-414
6148
878
--
0.15%
--
128
2.3
158
3.62%
333
1.47
104
1.49
381
1.30
0.750
Sediment Fraction
Exchangeable Interstitial Elutriate
mg/kg Water - mg/1 mg/1
__
__
__
--
--
2.3 1.4
--
88.8 -- (3.49)
0.50 0.12 0.14
1.09 0.16 (0.14)
1.6 0.10 0.06
2.5 0.18
114 5.1 0.49
0.55 0.15 (0.16)
62.4 6.4 9.6
0.62 0.48 0.46
4.0 0.12 0.04
__
—
                             334

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        TABLE 4.   CONTAMINANT  CONCENTkAl1UNS IN I HE  TISSUE  OF  THE  MUSSEL
                  Mytilus edulis  IN THE CHEMICAL UPTAKE STUDY  IN THE
CONTAMINATED
SEDIMENT PHASE OF THE ESTUARINE TEST

SS
g/i
At col
0
0
0
0
0
3.6
12.1
15.9
Exposure
days
lection
3
10
15
21
P
P
P
P
Metals (pg/g wet)

0
0
0
0
0
0
0
0
0
As
.oy
.15
.15
.28
.6
.06
.16
.10
.08
Cd
0.96
0.09
0.32
0.26
0.44
0.28
2.15
1.16
1.07
Cu
2.05
5.98
1.74
1.16
1.14
0.85
5.22
2.43
2.83
Fe
71
176
131
100
95
49
154
55
58
Pb
U. 19
0.15
0.19
0.23
0.18
0.15
1.68
0.34
0.18
Mn
2.71
7.74
3.29
1.16
3.09
3.49
2.99
2.92
1.95
Hg
0.15
0.12
0.05
0.02
0.06
0.02
*
*
0.11
Ni
0.68
1.24
0.94
1.74
2.60
3.15
2.72
1.46
1.17
Zn
38.4
45.6
25.0
20.2
39.1
27.5
100.0
55.9
50.0

P = Animals were exposed to indicated suspended solids concentration for 21
    days then placed in clear water 5 days to purge the sediment from the
    digestive tract and body surfaces before analyses.

* = Insufficient sample for analysis.
   TABLE 5.   WHOLE BODY CONCENTRATIONS OF SELECTED METALS IN CHEMICAL UPTAKE
             STUDY WITH CONTAMINATED SEDIMENT IN THE MARINE TEST

Species
Mytilus
edul i s
Mytilus
cal ifornianus
Crangon
nigromaculata
Cancer
magister

Suspended
Solids
Exposure
Control
Purged
Control
Purged
Control
Purged
Control
Purged

As
0.12
0.20
0.17
0. 12
0.03
0.08
0.03
0.03

Cd
0.34
0.10
0.51
0.45
0.06
0.23
0. 10
0.13

Cu
2.48
7.66
3.52
9.23
4.95
9.08
16.8
13.3
Metals
Fe
154.0
215.0
162.0
88.8
38.8
25.6
55.9
51.4
(Mg/g
Pb
2.14
3.89
0.97
2.28
0.55
0.27
0.31
0.38
wet)
Mn
2.53
2.48
1.62
0.95
0.87
8.20
1.00
8.06

Hg
0.63
0.02
0.21
0.03
0.13
0.14
*
*


Ni
0.
0.
0.
0.
0.
0.
0.
0.
04
05
08
004
01
52
19
37

Zn
25.7
33.6
22.7
25.0
7.2
22.7
13.3
16.8

* -
  = Insufficient sample for analysis.
                                      335

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       TABLE 6.   CONTAMINANT CONCENTRATIONS  IN  THE  TISSUE  OF  THE  MUSSEL
                 Mytilus edulis IN THE CHEMICAL UPTAKE STUDY  IN THE
                 CONTAMINATED SEDIMENT PHASE OF THE ESTUARINE TEST

ss
g/i

Exposure
days DDE
Chlorinated Hydrocarbons (ug/g wet)
Total Aroclor
DDD DDT DDT 1241 1254 1260

Total
PCBs
 At collection     0.68    0.32
 0         3       1.18    0.38
 0        10       0.52    0.84
 0        15       0.50    0.46
 0        21       0.18    0.85
1.00
1.56
1.36
0.96
1.03
0.02
0.02
0.02
0.02
0.04
0.05
0.06
0.03
0.06
0.02
0.01
0.01
0.01
0.02
0.01
0.08
0.09
0.06
0.10
0.07
0
3.6
12.1
15.9
P
P
P
P
0.55
0.75
0.49
0.47
0.40
0.83
1.10
0.68
0.95
1.58
1.59
1.15
0.06
0.07
0.05
0.05
0.02
0.07
0.03
0.02
0.01
0.02
0.02
0.01
0.09
0.16
0.10
0.08

P = Animals were exposed to indicated suspended solids  concentration for 21
    days then placed in clear water 5 days  to purge  the sediment from the
    digestive tract and body surfaces before analyses.
- = See note Table 7.
          TABLE 7.   WHOLE BODY CONCENTRATIONS OF SELECTED CHLORINATED
                    HYDROCARBONS IN CHEMICAL UPTAKE  STUDY WITH CON-
                    TAMINATED SEDIMENT IN THE MARINE TEST

Species
Mytilus edulis
Mytilus
cal ifornianus
Crangon
nigromaculata
Cancer magister

Suspended
Solids
Exposure
Control
Purged
Control
Purged
Control
Purged
Control
Purged
Chlorinated Hydrocarbons
DDE DDD DDT
1.71 - 0.69
2.02
1.66
2.57
1 . 54
1.39
0.14
0.14
(M9/9)
DDT
2.40
2.02
1.66
2.57
1.54
1.39
0. 14
0.14

- = Below detection limits;  DDD < 0.006 ng/g;  DDT <  0.008 ng/g.   Also below
    detection limits were aldrin, dieldrin,  heptachlor <0.004 ng/g;  chlordane
    < 0.008 ng/g;  endrin, PCBs < 0.1  ng/g.
                                     336

-------
the freshwater clam,  Corbicula  sp. ,  were exposed to contaminated sediments in
order to determine magnitudes of uptake of hydrocarbons which were included in
sedimentary  oil  and  grease burdens.  Sediment  characteristics  are  shown in
Table 8.

     There was no  overt  mortality of test organisms that was directly attrib-
utable to  exposure to contaminated  sediments.  Experimental  evidence as pre-
sented in  Table  9  suggested slight  uptake of hydrocarbons  by  saltwater test
organisms  incubated  in the  presence of  Duwamish  River sediments  which con-
tained almost  500  ppm total hydrocarbons  (11).  Freshwater  clams  exposed for
30 days to Duwamish River sediments showed no well-defined uptake of hydrocar-
bons (11).  As presented  in Table 10, mussels and crabs exposed for 4 days to
New York  Harbor  sediments containing 2000 ppm total hydrocarbons showed aver-
age  uptakes  above  background of  about  50  to  70  ppm  (2.5  and  3.5  percent,
respectively, of  the sedimentary hydrocarbon concentration).

     These  results  (11)   indicated  that  selected  estuarine and  freshwater
organisms can  be exposed  to dredged material that is contained with thousands
of parts per million oil  and grease and experience minor mortality for periods
up to 30 days.  Uptake of hydrocarbons from the heavily contaminated sediments
appears minor  when  compared to  the  hydrocarbon content  of  the  test sediments
and when  compared  to  results describing  exposure  of uncontaminated organisms
under field  conditions where total  hydrocarbon uptake  ranged to  several hun-
dred parts per  million (12).

     In Work Unit 1D07 (13), attempts were made to trace pathways of uptake of
sediment-associated DDT into  the  tissues of estuarine deposit-feeding benthic
infauna.   The  data obtained suggested the possibility of uptake  of DDT under
model  laboratory conditions  which  may  or may not  be operative  under field
conditions.  Fulk,  Gruber,  and Wullschleger (14)  have reviewed the literature
on pesticides  and  PCBs  in sediments.  Algae, suspended  solids,  bottom sedi-
ments, and  water contain various chlorinated  hydrocarbons.   The  studies con-
ducted on  the  adsorption  and desorption of chlorinated hydrocarbons on solids
have generally indicated  that  the materials are  much more readily sorbed than
desorbed.  These workers  analyzed the  sediments  from  five  locations for al~
drin,  dieldrin,  endrin,   lindane,  2,4-D  esters,  DDT analogs, toxaphene,  and
PCBs.  PCBs,  dieldrin, and the  DDT analogs  were  the most  prevalent.   The
desorption of  the  latter  materials  was  studied.   No  release of  DDT residues
was  observed.  Some  dieldrin release  was observed  in  the parts  per trillion
range.   On the basis  of  these laboratory  studies,  it  appears  that release of
these  water-insoluble pesticides  will  not  occur  to  an appreciable  extent
during disposal.    In  another study,  Anderlini  et  a!.  (15)  monitored release
from sediments and  uptake by organisms of PCBs and compounds of the DDT group
during a disposal operation  in San Francisco Bay.   Some uptake of p,p'-DDE was
observed  but  the levels  of the other chlorinated  hydrocarbons  remained con-
stant in  Myti1 us  edulis.
                                      337

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338

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                        TABLE 9

    HYDROCARBON ANALYSES BY TLC OF CRABS (Hemigrapsus
oregonensis) EXPOSED TO DUWAMISH RIVER DREDGED MATERIAL



Tank Seri

SED
SED, Ref
SCR
SCR, Ref
STR
STR, Ref
Hydrocarbon
es* Time Days Alkanes
0 14
17 22
17 8
17 21
17 19
17 25
17 10
Content ug/g dry ti
Arenes
2
7
3
14
10
6
5
ssue (ppm)
Total
16
29
n
35
29
30
15
HYDROCARBON ANALYSES BY TLC OF MUSSELS (Mytilus
edulis) EXPOSED TO DUWAMISH RIVER DREDGED MATERIAL



Hydrocarbon
Tank Series* Time days Alkanes

SED
SED, Ref
SCR
SCR, Ref
STR
STR, Ref

0 143
30 35
30 48
30 84
30 35
30 110
30 63
HYDROCARBON ANALYSES BY TLC OF SNAILS

Content pg/g dry ti
Arenes
35
58
47
54
<6.5
52
15
(Acanthi na spirata)

ssue (ppm)
Total
178
93
95
138
<41.7
162
78

EXPOSED TO DUWAMISH RIVER DREDGED MATERIAL

Hydrocarbon
Tank Series* Time days Alkanes

SED
SED, Ref
SCR
SCR, Ref
STR
STR, Ref
0 <6
30 14
30 4
30 CO
30 6
30 28
30 CO
Content ug/g dry ti
Arenes
<4
7
4
NTAMINATE
2
37
NTAMINATE
ssue (ppm)
Total
<9
21
8
D
8
65
D

* = SED -
SCR -
STR -
Ref -
Organisms in sediment.
Organisms on screen 5 cm above sediment
Organisms on screen 30 cm above stirred
Reference sediment.

.
sediment.





                           339

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                                   TABLE 10

      HYDROCARBON ANALYSES BY TLC OF CRABS (Hemigrapsus  oregonensis)  AND
MUSSELS (Mytilus

edulis)

EXPOSED TO PERTH AMBOY (NJ)
DREDGED
MATERIAL

Tank Series*
Crabs


STR #1

STR #2

Mussels

STR #1

STR #2

Time days
0
0
4
4
4
4
0
4
4
4
4
HYDROCARBON ANALYSES BY
MUSSELS (Mytilus edulis

Tank Series*
Crabs

SED
SCR
STR
Mussel s

SED
SCR
STR

Time days
0
1
1
1
0
27
27
27
Hydrocarbon Content
ug/g dry
Alkanes Arenes
19
21
47
59
66
85
17
22
28
18
20
TLC OF CRABS (Hemigrapsus
) EXPOSED TO BAY RIDGE (NY)
Hydrocarbon Content
6
7
21
34
42
35
46
65
76
86
143
tissue (ppm)
Total
25
28
68
93
108
120
63
87
104
104
163
oregonensis) AND
DREDGED
Mg/g dry
Alkanes Arenes
62
58
24
70
25
72
23
108
11
22
5.2
22
22
121
32
180
MATERIAL
tissue (ppm)
Total
73
80
30
92
46
193
55
288

* = SED - Organisms in sediment.
    SCR - Organisms on screen 5 cm above sediment.
    STR - Organisms on screen 30 cm above stirred sediment.
                                      340

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                             FIELD INVESTIGATIONS

FRESHWATER SITE

     The Ashtabula, Ohio, ADFI site is located in Lake Erie (16) just north of
the entrance to Ashtabula Harbor (Figure 1).  The movement of surface water in
the lake is counterclockwise although reversals do occur with northeast winds.
A compensating current  is  found in the deeper waters of the lake during ther-
mal stratification  (June-October).  Because  of the  configuration of the lake,
any contaminants which  are  released along the south  shore  tend to move east-
ward along the  shore.   Oxygen depletion occurs in the deeper water during the
summer.

     Sediment  in the  disposal area primarily  originates  from  material  trans-
ported  by  the  longshore current  and,  to a lesser extent,  from the Ashtabula
River which enters  Lake Erie through Ashtabula Harbor.  The sediment consists
of about  equal  parts of sand  and  silt, with a small  amount  (<10  percent) of
clay.  There is apparently little variation in grain size with depth.

     Although  there have  been severe  water  quality problems  in  the  lake,
striking improvements have  been noted in recent years.  At the Ashtabula ADFI
site,  water quality variables tended to be quite uniform throughout the water
column  except during  stratification.   The  expected  differences resulting from
stratification were observed;  during  periods  of upwelling,  deeper (hypolim-
netic) water was often found quite near the  surface.

     A  variety  of   invertebrates  and  fish  inhabit  the area.   The  former in-
cludes  mollusks,  worms, insect larvae, and  crustaceans.   These form  a  food
supply  for the  40-odd  species of fish which were observed.  Yellow perch were
the most abundant  species,  with alewife, gizzard shad, and white sucker being
quite common.   Moderate to abundant populations of both zooplankton and phyto-
plankton occur throughout the  lake.

     The Ashtabula  area is  heavily industrialized and  is  a major  port facil-
ity.   There are  a  number  of industrial and agricultural  sources  of contami-
nants in  the  immediate vicinity  and  there   are  two  fossil-fuel  generating
stations east of Ashtabula.   These  discharge almost 2300 x 106 I/day of cool-
ing and  waste water  into Lake Erie.

     The Ashtabula  ADFI spanned 3 years  (1975-1977).   The  study consisted of
four  phases:   a pilot  survey  (1975),  predisposal  sampling  (1975),  disposal
operations  (1975-1976), and  postdisposal  sampling  (1975-1976).   Samples for
various  parameters  were obtained  from a disposal area and  an adjacent refer-
ence area.

     The  physical   variables  measured  included  currents,  temperature,  light
transmission,   meteorology,  waves,  bathymetry  and sub-bottom  profiles,  grain
size,  sedimentology, and hydrology.

     Both pumped samples  and grab samples were  obtained  for analyses of con-
ductivity,  pH,  turbidity,  dissolved  oxygen,  nutrients,  alkalinity,  metals,
organic  carbon, silicates,  and  sulfate  in the  water column.  Bulk sediment and


                                       341

-------
           LAKE   ERIE
                      DISPOSAL
                        AREA
REFERENCE
   AREA
(ALTERNATE)
Figure  1.  Locations  of disposal and reference areas,
         Ashtabula  River disposal site, Ohio.
                   342

-------
sediment interstitial  water were  analyzed  for nutrients,  metals  and organic
carbon; bulk  sediments were  further  examined for pH, Eh,  percent water,  and
cation exchange  capacity.   In addition, in-place sediment  oxygen  demand mea-
surements were carried  out.

     Phytoplankton and zooplankton  samples  were evaluated in terms of species
present and abundance; primary  productivity was estimated by pigment analysis
and carbon-14  uptake.  Elutriate from dredged samples was added to phytoplank-
ton samples  to determine  if  inhibitory or  stimulatory  effects  were present.
Bottom grabs  were  obtained for  investigation of macro- and meiobenthic organ-
isms.   As  with plankton,  these samples were evaluated to determine the numbers
and kinds of organisms  present.

     A variety of  fishery studies were carried out.   These included sampling
with gill   nets and otter trawls, tows for fish larvae, age determination,  and
examination of stomach contents.   Both  fish and invertebrates  were analyzed
for heavy metals.

Findings

     Spring and  summer disposal  by hopper dredge resulted in the formation of
mounds of  dredged  material  in the disposal area.  These mounds (16) were 30 to
50 cm high, and, rather than a single mound being present, there were numerous
small   mounds.   Disposal  also created  a small  (<  2ฐC)  transient  increase of
temperature in the water column; during thermal  stratification,  disposal  did
not alter  the thermal  structure.   There was little  change in grain size after
disposal  and   those  few   changes  observed  had  disappeared  within  3  months.
Erosion of the mounds occurred  as a  result of  fall  and  winter  storms,  and
there was a new transport of material to  the northwest and southeast.

     Almost all  of the  chemical  variables  measured in  the  water  column were
affected by  disposal   (16).   Effects  were  not  great,  however, and  an essen-
tially complete  return to  ambient predisposal  conditions  was  noted within a
few minutes to several weeks.   The overall  impact of disposal is not clear as
some  constituents  increased,  presumably  through  release,  while   others  de-
creased.   The  latter phenomenon  probably  resulted from sorption into settling
dredged material.

     There were  changes   in  interstitial  water (of  sediment) chemistry after
disposal  (16).   A  return  of  predisposal  conditions  took from 30  to 90 days.
It should  be  kept  in mind that the sediments were eroding and being compacted
and/or  reworked  after disposal.   This  process  in  itself could  bring about
various changes in  interstitial water chemistry.

     The greatest chemical effect of disposal appears to have been observed in
the sediment.   Following disposal, nutrients  increased in  the  sediment,  but
metals (except mercury)  decreased.  This  effect  is not  surprising  as  it  re-
flects the relative  concentrations of nutrients in  lake  sediments and harbor
sediments.

     Overall   interpretation of the results of sediment chemistry are difficult
because of the behavior  of dredged material when released  and of the natural
                                      343

-------
lake sediments.  Rather than  there  being an overlay of  dredged  material  upon
natural lake bottom,  the  physical  impact of the dredged material striking the
bottom resulted  in  bottom currents.   These  currents pushed lake bottom to the
periphery of the  study  area and on top of previously deposited dredged mater-
ial.  Hence, alternating series of dredged material  and natural bottom result-
ed, with subsequent  compaction and reworking serving to  further obscure  dif-
ferences between the  two sediment types.

     Disposal  operations  at  Ashtabula  had  essentially no  measurable  impact
upon planktonic  organisms (16).  Benthic  organisms were  impacted  in several
ways.   There was  no change in  the  number of species present  in the disposal
area following  disposal,  but  there were a number of changes in species compo-
sition, with new species transported from the harbor replacing those which had
been eliminated.   In addition, there  was a  large  increase  in  the  number of
organisms in the  disposal  area.   Many of the changes  did  appear to be initi-
ally  confined   to  the  immediate  area of  disposal.   As  erosion spread  the
dredged material over a  larger area,  faunal changes in the expanded area were
observed.   Of  interest was  the finding that gross  animal  groups (such as the
family  level   of  identification)  were  not  sufficient  to  determine impacts;
rather, an examination at the species level was required.

     Adults  and young of  pelagic  fish did not appear to be impacted by dispo-
sal.  However,  bottom-dwelling fish showed a negative response to disposal and
migrated from  the area.   Within an hour after disposal  these fish had migrated
back into the  disposal  area.   Overall, the effects  of disposal upon fish were
of small  magnitude  and only persisted for a short period of time.

     Heavy metals in fish and invertebrates, as presented in Tables  11 and 12,
showed little  change  as  a result of  disposal.  The  relative  concentration of
metals  in  fish were  the  same  as  those observed in  the  sediment,  whereas  a
decrease was noted in some of  the  invertebrates.   Hence,  bioaccumulation did
not occur.

ESTUARINE SITE

     The Duwamish  River  enters Elliott Bay, a part  of Puget Sound (Figure 2).
The entire river is tidal  with horizontal and vertical  variations in salinity.
These  depend  upon tidal  stage and river discharge.   Low  (<3-mg/l)  dissolved
oxygen  concentrations  occur  near  the  bottom  of  the  river.   Although  quite
important as  a waterway,  the Duwamish  is  also a  major migration  route for
salmon and trout.

     Elliott Bay  is  a  rather  typical  estuarine system with a surface layer of
low salinity water being  present  over  a  deeper layer  of  more  saline water.
During the  summer,  density stratification is present but in the winter colder
freshwater  from the  waterway  entrains  and mixes  with warmer  saline  water.
Hence,  there  is usually  no  stratification  in  the  winter.   Because  it  is an
estuary, water column  chemical constituents tend to  be rather variable.   The
waterway has created an underwater delta along the south side of the bay.   The
deltaic  sediments  consist  mainly  of  silty  sand  mixed  with wood  and  other
organic debris.  The dominant  demersal  fish in the bay  during the  winter are
assorted  soles,  and  the  dominant  benthic  invertebrate  is the  pink shrimp.
Worms and various mollusks are also important components  of the bottom fauna.


                                       344

-------












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-------
                                        REFERENCE
                                        SITE B
                          EXPERIMENTAL
                          DISPOSAL SITE
                                 4
               REFERENCE
               SITE A
                          MOUTH OF DUWAMISH
                                D
                                44
                                             .V DUWAMISH
                                               RIVER  '
          DUWAMISH.-.
          RIVER
          STATIONS
Figure 2.   Locations  of Duwamish Waterway disposal and reference sites,
           Puget Sound, Washington.
                               346

-------
     Dredging has ordinarily been done in the waterway with an hydraulic pipe-
line dredge and  upland  disposal  has been used.  However,  the  increasing cost
of  upland  disposal  required  a shift  to  the use  of mechanical  dredging  and
open-water disposal  with  barges.   In  1974,  there was a spill of almost 1000 1
of PCBs at Slip  1,  in the maintenance dredging area of the river.  The highly
contaminated  sediments were  hydraulically  dredged  and placed in an impervious
containment  area (17)  while  the  remaining,  less  contaminated  material  was
removed by a  clamshell dredge, placed in barges, and transported to the exper-
imental disposal  site.  The  dredging and disposal of  the  highly contaminated
sediments  were  carefully  monitored  by  the  Environmental  Protection  Agency
(EPA).   The EPA  found that  there was a minimal  release  of metals, nutrients,
and hydrocarbons  (17).

     The ADFI  was divided into four phases:  a pilot  survey and predisposal,
disposal monitoring,  and  postdisposal  studies.   During the  pilot survey,  an
experimental  disposal  site  was  chosen for disposal,  and  two  reference sites
(to the east and west)  were  selected  to provide  comparative data (Figure 2).
The studies were  initiated in  1975 and completed  in 1976.

     Physical  investigations  conducted for the various  phases  included grain
size analyses  and measurements  of currents, waves,  light transmission, fall
velocity of  dredged material, and the vertical distribution of dredged mater-
ial in  the water column following disposal.  In addition,  sub-bottom profiles
and the overall bathymetry of the area were obtained to estimate the volume of
material disposed of at the site.

     Chemical  studies were  carried out on the water column and the sediments.
Variables  measured  in the water column  included  temperature,  turbidity, sus-
pended  solids,  dissolved  oxygen,   pH,  salinity,  nutrients,  PCBs,  and heavy
metals.   Several approaches  were  employed  in the  measurement  of  sediment
variables.   These were bulk analysis, interstitial water, and elutriate tests.
In all  cases,  PCBs  and  heavy metals were  evaluated.   Nutrients were analyzed
only in interstitial  water  and  during  the  elutriate  testing.   Bulk analyses
included percent water,  volatile solids, organic carbon, sulfides, Eh, pH, and
oi1 and grease.

     Bottom grabs were taken  to characterize the types, abundance, and biomass
of benthic organisms.   Dermersal  organisms were collected by trawling and were
analyzed in  terms of  species composition, number/unit  of  effort, length, and
weight  for dominant  finfish.   Diet studies  for  finfish  were also undertaken.
The concentrations of PCBs  and heavy metals  in the  tissue of fish and shrimp
were determined  to evaluate uptake and/or bioaccumulation of these substances.
In  addition,  organisms  were  suspended in  cages  over the  disposal  mounds to
examine toxicty and uptake of  contaminants.

Findings

     The dredged material  was an oily, black, fine organic silt with a plastic
texture.   It was found to  leave  the  disposal  barge  in clumps  or as a well-
defined mass and fall to  the  bottom with velocities  of  up  to  180  cm/sec.  Upon
impact  with  the  bottom,  a dense surge  of  material  flared  outward at about 36
cm/sec  and could be  detected more  than  200  m from the point of  impact.  Sus-
                                      347

-------
pended  solids  returned  to ambient  conditions within  10  min,  but  a  slight
reduction in light transmittance persisted for several  hours  (18).

     The disposal of 114,000 m3 resulted in numerous mounds  2 to 3 m in height
with a  maximum  radius  of  approximately 200  m.   Subsequent chemical  analyses
for PCBs at  6  and  9 months after disposal  indicated that the mound was gradu-
ally  spreading  (18).   This movement  was probably  brought  about  by  currents
gradually  redistributing  the  dredged  material.    The  spreading  was  not  of
sufficient magnitude to  move  the contaminated sediments beyond the boundaries
of the disposal site.

     The majority of chemical  changes  in the water column during disposal were
relatively minor (18).   There  were  increases in dissolved manganese,  ammonia,
phosphorous, and total   PCBs.   These  changes occurred with  increases in sus-
pended particulate matter,  and,  when  particulate  matter decreased, so did the
concentrations of contaminants.  The  increase in  particulate matter and asso-
ciated chemical  variables  was  of extremely short duration,  usually less than
30 minutes.  It  is  of  interest that,  prior to disposal, the concentrations of
PCBs  in  the water  column  exceeded  EPA criteria  and  these  concentrations in-
creased  after  disposal.   It is  possible that PCBs were  entering  Elliott Bay
from the  Duwamish  Waterway and  had  approached equilibrium saturation values
prior to disposal.

     As would be expected,  the chemical changes observed in the sediment are a
reflection  of  the nature  of  the dredged  material  (18).   Metals,  nutrients,
PCBs, and oil and grease were present  in the disposal  area sediment in greater
concentrations after disposal than before disposal.

     A  number  of biological  variables  were  investigated during  the  Duwamish
ADFI and  a few  showed major  changes  as a result of  disposal.  The number of
species,  density,   biomass,  and  diversity  of  benthic  invertebrates  at  the
disposal  site  were  depressed after  disposal  (when  compared  to  predisposal
values)  (18).  These  effects  were  most apparent  for the central  stations of
the  disposal   site  and  least  noticeable for  the corner stations.   Some de-
creases in the above parameters were also noted at the two reference stations.
Nine months  after disposal  the number of species  present at the disposal site
was comparable to the  numbers  present at the two  reference sites  although the
biomass values continued to  be depressed for the  central and side stations of
the disposal site.  There  was  evidence that animals at the edges  of the disp-
osal site were  stimulated by the dredged material.

     As  presented  in Tables  13  and  14,  there was  essentially no uptake of
metals  or  PCBs  by  fish  or most  invertebrates  analyzed during and after the
disposal operations.  Pre-  and post-disposal  specimens were collected from the
disposal  site  and  locations  outside  Elliott  Bay  (18).  In  addition,  caged
animals were  held  at  the  disposal  site  for up  to 3 weeks.   Mussels held in
cages at the disposal  site  accumulated PCBs to levels above background but the
increase was  not statistically  significant.   It  should be  pointed out, how-
ever,  that  some  of the  animals  collected  from Elliott  Bay  prior  to  disposal
contained  substantial  amounts  of PCBs  so a  slight uptake may not have been
statistically significant.
                                      348

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                      TABLE 13
MERCURY AND CHROMIUM CONCENTRATIONS IN SEA CUCUMBERS

Exposure
(weeks)
0
1
2
3

Exposure
(days)
0
3
3
7

Exposure
(weeks)
0
2
5
14
27
39
Sample
XIXIXI XI
MERCURY
Sample
XIXIXI XI
MERCURY AND
Sample
X
X
X
X
X
1
Mercury, ppm
Disposal West
Site Reference
Predisposal
0.01 0.01
Postdisposal
0.01 0.01
0.01 0.01
0.01 0.01
AND CHROMIUM CONCENTRATIONS
Mercury, ppm
Disposal West
Site Reference
Predisposal
0.06 0.06
During Disposal
0.06
0.06
0.07
CHROMIUM CONCENTRATIONS IN
Mercury, ppm
Disposal West
Site Reference
Predisposal
0.08 0.06
Postdisposal
0.06 0.06
0.07
0.05 0.06
0.04 0.05
0.04 0.05
Chromium
Disposal
Site
0.32
0.26
0.26
0.26
IN SPOT SHRIMP
Chromium
Disposal
Site
0.64
0.62
0.61
ALASKA PINK SHRIMP
Chromium
Disposal
Site
0.83
0.68
0.63
0.55
0.50
0.62
, ppm
West
Reference
0.32
0.24
0.24
0.24

, ppm
West
Reference
0.64
0.57

, ppm
West
Reference
0.63
0.62
0.67
0.58
0.70
                         349

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                                   TABLE 14
            PCBs IN MUSSELS (Mytilus edulis) EXPOSED AFTER DISPOSAL




West Reference Site:


Disposal Site:


Exposure (weeks)
0
1
2
3
1
2
3
Mean ppm
0. 122
0.103
0.131
0.100
0.108
0.200
0.206
 PCBs IN SPOT SHRIMP (Pandalus platyceros) EXPOSED DURING DISPOSAL OPERATIONS

                                     Exposure (days)                  Mean ppm

West Reference Site:
Disposal Site:

0
7
3
3
0. 174
0.190
0.208
0.185
                   PCBs IN ENGLISH SOLE (Parophyrys vetulus)
                                     Sampling period                  Mean ppm
West Reference Site:                  Before Disposal:                   2.28

                                     After Disposal:

                                        2 weeks                        0.65
                                        1 month                        0.87
                                        3 months                        *
                                        6 months                        *
                                        9 months                       5.90**

Disposal Site:                       Before Disposal:                   2.58

                                     After Disposal:

                                        2 weeks                        0.74
                                        1 month                         *
                                        3 months                        *
                                        6 months                        *
 * = No samples.
** = One samp le only.
                                     350

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     Demersal  fish  and shellfish  (shrimp)  seemed  to  ignore disposal.  (here
were  fewer present  during  disposal  at  the  disposal  site  than at  the east
reference  site but about the same number as at the west reference site.  After
disposal the  number  of fish decreased at the disposal site and at both refer-
ence sites; this decrease suggests a seasonal change in these organisms rather
than an  impact of  disposal (18).  The number of shrimp captured at the dispo-
sal site after disposal  increased compared to those  obtained prior to dispo-
sal.  Shrimp  at the  reference  sites  either remained at  the  same  level  (east
reference  site)  or  increased erratically from month  to  month (west reference
site).  Overall, more shrimp were  found at the  disposal  site  after disposal
than  at  either  reference  site,  indicating that the  shrimp  were attracted to
the disposal site.
                                    SUMMARY

LABORATORY INVESTIGATIONS

     Research  results  show  that  in  general  dredged  material   in  the United
States is  not  as  toxic to aquatic organisms as originally conceived, based on
bulk  sediment  analysis.   Nevertheless,  some sediments  are  toxic and disposal
of these sediments may  cause environmental harm.

     DMRP Work Unit 1D06 (4) evaluated the possibility of obtaining a chemical
extraction method  for  sediments which would reflect the availability of heavy
metals to  organisms.   Studies  to date have not produced such a technique, and
there  is  no chemical  method  for  environmental  impact evaluation  of dredged
material prior to  its  disposal.  DMRP Work Unit 1D11 (11) showed that although
oil and grease levels  could be  high in sediments, a large part of what is rou-
tinely  reported  as oil  and grease  may  be  harmless  elemental   sulfur,  and a
large  part  of  the hydrocarbon  burden of  sediments  is  not released from sedi-
mentary particles nor  is it available for gross uptake into the aquatic organ-
isms tested.

     Bioaccumulation by itself  is difficult to interpret in terms of toxicity.
Accumulation of a known  toxicant in  a human  food source is of obvious impor-
tance.  Components can be transferred through  aquatic food chains with biomag-
nification.  Accumulation may stress the organism and make it more susceptible
to disease or predation.  Necessary energy may have to be diverted into detox-
ification mechanisms.  Lowered  fecundity  and abnormal  larval development will
ultimately  have  effects  on  species  abundance and  population  dynamics within
localized  systems.  These kinds of sublethal effects can culminate in an unex-
plainable population decline over an extended period of  time.

FIELD INVESTIGATIONS

Freshwater site

     There were but few important impacts as a result of dredged material dis-
posal  at  the Ashtabula  disposal site.    Some  chemical  changes  were observed,
but these were of  small magnitude and transient in  nature.  There were changes
in the benthic community which  persisted throughout the study; these primarily
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consisted  of  species  replacement and  an  increase in  the abundance  of  some
organisms.   Because  these  benthic  organisms  are of  importance  as  food  for
fish, these changes  would  be of concern were  it  not  that the feeding activi-
ties of  fish in the area did not  seem to be altered.

Estuarine Site

     Disposal  of  material  contaminated  with  PCBs in  Elliott Bay  during  the
Duwamish Waterway  ADFI appeared  to  have a minimal impact.   A  disposal  mound
was created which gradually spread during the postdisposal period.  There were
minor changes in  the chemistry  of the water column.   These appeared to be as-
sociated with a transitory increase in suspended particulate material, and, as
soon as  this  material  had settled, values for chemical parameters returned to
predisposal conditions.

     There was no significant uptake of PCBs or metals by organisms inhabiting
the  disposal  area or  by caged  animals  which  were held  in  close  proximity to
the  disposed  material  for  up  to 3  weeks.   Some changes  were noted  in  the
abundance, diversity,  and  species  composition of benthic invertebrates in the
disposal area; however, similar changes in the reference area populations make
it unlikely that disposal was wholly responsible for the changes.

APPLICATION AND REGULATION

     The  conceptual  problem  of toxicants associated  with sediments  must be
evaluated in light of valid chemical  and biological data describing the avail-
ability  of  toxicants  to  organisms  and the water  column  prior  to determining
effects  of such  toxicants (2).  Information  must then  be  gained as  to  the
effects  of specific  substances  on organism survival and function.   Many mater-
ials previously  regarded  as  toxicants  are not  readily  desorbed  or  released
from sediment attachment  and are thus  less toxic  than in the free or soluble
state,  on which most  toxicity data are  based.

     Prater  and  Anderson  (19),  using  a 96-hr  bioassay technique with  four
different species  or organisms, evaluated the toxicity  of  sediments  from the
Ouluth,   Minnesota-Superior,  Wisconsin   harbor.   Sediments  could  be  broadly
classified  on  an arbitrarily selected  scale  as  nonpolluted,  moderately pol-
luted,   and  heavily  polluted  using the bioassay.   The results  of  an  array of
chemical analyses  also led to an arbitrary designation of nonpolluted, moder-
ately polluted,  and heavily  polluted sediments.   In  75  percent  of the cases
chemical analyses supported bioassay results,  but they were unable to identify
the  causal chemical  factor  for  mortality.  Concentrations of chemicals thought
to  be pollutants  varied from one station to another and were not always high-
est  at  stations  producing highest mortalities.  Toxic properties of sediments
could have  been  due to  the  action of one or  more pollutants acting  together
(synergism) or  to unidentified  contaminants,  particularly organic compounds.
This strongly  argues  for  the use of  a whole-sediment  bioassay  to determine
potential  toxicity  of  dredged material  for disposal  (20).   Although  the sug-
gested  procedures  have yet  to   be  fully evaluated under a wide  spectrum of
environmental conditions,  experience  will  undoubtedly validate  this  type of
test over the  long term.
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     There are now cogent reasons for rejecting many of the conceptualized im-
pacts of disposed dredged material regarding potential toxicity based on clas-
sical bulk analysis  determinations.   It is invalid to use total sediment con-
centration to estimate  contaminant  levels in organisms  since  only a variable
and  undetermined amount of  sediment-associated contaminants  is  biologically
available.  Although a  few  instances of  uptake of  possible  ecological  conse-
quence have been  seen,  the  fact  that  uptake  depends  on species,  contaminants
salinity,  sediment  type, etc.,  argues strongly that  bulk analysis  does  not
provide a  reliable  index of contaminant availability and potential ecological
impact of dredged material.


                                  REFERENCES

 1.  Fpurth Annual  Report:   Dredged  Material  Research  Program, Environmental
     Laboratory, USAE Waterways Experiment Station, Vicksburg, MS,  Jan 77.

 2.  Hirsch,   N.   D. ,  DiSalvo,   L.  H. ,  and  Peddicord,  R., 1978.   "Effects  of
     Dredging and Disposal  on  Aquatic  Organisms,"  Tech.  Rept.  DS-78-5,  USAE
     Waterways Experiment Station, Vicksburg, MS.

 3.  Wright,   T.  D. ,  "Aquatic Dredged Material  Disposal  Impacts,"  Tech.  Rept.
     DS-78-1,  1978,  USAE Waterways Experiment Station,  Vicksburg, MS.

 4.  Neff, J.  W. ,  Foster,  R.  S., and Slowey, J. F.  "Availability of Sediment-
     adsorbed Heavy Metals  to  Benthos with  Particular Emphasis  on Deposit
     Feeding  Benthos,"  Tech.   Rept.   D-78-42,  1978,  USAE  Waterways Experiment
     Station,  Vicksburg, MS.

 5.  DiSalvo,  L. H.  , et al. , "Assessment and Significance of Sediment-associa-
     ted Oil  and  Grease in  Aquatic Environments,"  1977.  Tech. Rept. D-77-26,
     USAE Waterways Experiment  Station,  Vicksburg, MS.

 6.  Brannon,  J.  M. ,  "Evaluation of  Dredged Material  Pollution  Potential,"
     Tech. Rept. DS-78-6, USAE Waterways Experiment Station, Vicksburg, MS.

 7.  Anderlini,   V.   C. , Chapman,  J.   W. ,  Girvin,  D.  C. ,  McCormick, S.  J. ,
     Newton,  A.   S. ,  and Risebrough,  R. W. ,  "Heavy  Metal  Uptake Study,  Dredge
     Disposal  Study, San Francisco Bay  and Estuary, Appendix H:  Pollutant Up-
     take Study," 1976,  U.S. Army  Engineer District,  San  Francisco, CA.

 8.  Simms, R.  R. ,  Jr.,  and  Presley,  B.  J. , "Heavy Metal  Concentrations  in
     Organisms  from an  Actively Dredged  Texas  Bay,"  Bull. Environ. Contam.
     Tpxicol., Vol 16, No. 5, pp 520-527.

 9.  Peddicord,   R.  K. ,  and  McFarland,  V. A.,  "Effects of  Suspended Dredged
     Material  on  Aquatic  Animals,"  Tech.  Rept. D-78-29,  July  1978,  by  Bodega
     Marine  Laboratory,  University   of  California,  under  contract to  USAE
     Waterways Experiment Station, Vicksburg, MS.

10.  Peddicord,   R.  K. ,  McFarland,  V.   A., Belfiori,  D.  P., and  Byrd,  T.  E. ,
     "Effects  of  Suspended Solids  on  San   Francisco  Bay  Organisms,"  1975,
                                       353

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     Dredge Disposal Study, San Francisco Bay and Estuary, Appendix G:  Physi-
     cal  Impact Study.  U.S. Army Engineer District, San Francisco, CA.

11.   DiSalvo,  L.  H. , Guard,  H.  E. ,  Hirsch,  N.  D. ,  and Ng, J. ,  "Assessment and      M
     Significance of Sediment-Associated Oil  and  Grease  in Aquatic  Environ-      ™
     ments," Tech.  Rept.  D-77-26,  November  1977,  prepared by Naval  Biosciences
     Laboratory,  Naval  Supply  Center,  Oakland,  CA,   under  contract  to  USAE
     Waterways Experiment  Station, Vicksburg, MS.

12.   DiSalvo,  L.  H. , Guard,  H.  E. ,  and Hunter, L.,  "Tissue Hydrocarbon Burden
     of Mussels  as  a Potential  Monitor of  Environmental  Hydrocarbon  Insult,"
     Environ.  Sci.  Techno!. ,  1975, Vol 9, pp 247-251.

13.   Nathans,  N.  W. , and  Bechtel,  T.  J. ,  "Availability  of Sediment-Adsorbed
     Selected Pesticides  to  Benthos  with Particular Emphasis on Deposit-Feed-
     ing Infauna,"  Tech.  Rept.  D-77-34,  Nov 77, prepared  by  LFE Corporation,
     Environmental  Analysis Laboratories, Richmond,  CA, under contract to USAE
     Waterways Experiment  Station, Vicksburg, MS.

14.   Fulk,  R.  , Gruber,  D. ,  and  Wullschleger, R.,  "Laboratory Study of the Re-
     lease  of Pesticide and  PCB Materials  to the  Water Column  During Dredging
     and Disposal  Operations,"  Contract Rept.  D-75-6,  Dec  75,  prepared  by
     Envirex,  Inc., Environmental  Sciences  Division,  Milwaukee,  WI, under con-
     tract  to  USAE Waterways Experiment Station, Vicksburg,  MS.

15.   Anderlini,  V.  C.,  Chapman,  J.  W.,  Newton,  A.  S.,  Risebrough, R.  W.,  "Pol-
     lutant Availability  Study,  Dredge  Disposal  Study, San  Francisco Bay and
     Estuary,  Appendix  I:   Pollutant Availability,"  1976,  U.S.  Army  Engineer
     District, San  Francisco, CA.                                                    A

16.   Sweeney,  R.  A., "Aquatic  Disposal  Field  Investigations Ashtabula  River
     Disposal  Site,  Ohio,"  Tech.  Rept.  D-77-42, 1977,  USAE  Waterways Experi-
     ment Station,  Vicksburg, MS.

17.   Blazevich,   J.   N.,  et al. ,  "Monitoring of Trace  Constituents  During PCB
     Recovery Dredging Operation -  Duwamish Waterway," 1977, U.S.  Environmen-
     tal  Protection Agency Rept. 910/9-077-039,  Region X, Seattle, WA.

18.   Tatem, H. E. ,  and  Johnson,  L.  H. ,  "Aquatic Disposal Field  Investigations
     Duwamish Waterway  Disposal  Site,  Puget Sound,  Washington,"  Tech.  Rept.
     D-77-24,  1977,  USAE Waterways Experiment Station,  Vicksburg,  MS.

19.   Prater,  B.  L. , and   Anderson,  M.   A. ,  "A 96-hour Sediment  Bioassay  of
     Duluth and  Superior  Harbor Basins  (Minnesota)  Using  Hexagenia  1imbata,
     Asellus  commum's,  Daphnia  magna,  and  Pimephales  promelas  as  Test Organ-
     isms," Bull. Environ.  Contam. Toxicol.,  Vol 18, No. 2, pp 159-169.

20.   EPA/CE Technical  Committee on  Criteria  for  Dredged and  Fill  Material,
     "Ecological  Evaluation  of  Proposed Discharge  of Dredged  Material  into
     Ocean  Waters;   Implementation Manual  for Section 103 of Public Law 92-532
     (Marine Protection, Research,  and  Sanctuaries  Act of 1972)," Jul  77, pub-
     lished by the Environmental  Laboratory,  USAE Waterways Experiment Sta-
     tion,  Vicksburg, MS.


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                      MANAGEMENT OF CONTAINMENT AREAS TO
                     PROMOTE DEWATERING AND SOLIDIFICATION
                              C.  C.  Calhoun,  Jr.
                           Environmental  Laboratory
               U.S.  Army Engineer Waterways  Experiment Station
                         Vicksburg,  Mississippi 39180


                                   ABSTRACT

     Methods  developed  by  the  Dredged  Material  Resarch  Program to  manage
dredged material  containment  areas  to  increase their service  lives  are dis-
cussed.    Emphasis  is  placed  on dewatering  fine-grained dredged  material  by
making maximum  use  of  evaporation.   Results of laboratory and  a  major field
study are given.   Methods of predicting dewatering attainable from evaporation
are depicted.
                                  BACKGROUND

     In papers presented  at  the previous two meetings (1, 2), information was
given on research being conducted as part of the U.S.  Army Corps of Engineers'
Dredged Material  Research Program (DMRP) on methods to dewater/densify dredged
material.    These  papers  were  prepared  at  a  time when  the research was  in
progress and  consequently complete results, conclusions,  and recommendations
could not be given.   The 5-year $33 million DMRP was successfully completed in
March and more definitive information can now be given on the results of these
studies.

     The results  of the  DMRP are  being  published in over  200  technical  re-
ports.   However,  final  results  and guidelines  from the program are being pub-
lished  in a  series  of 21 concise  synthesis  reports  and  most of the synthesis
reports will  also be  published as Corps  of Engineers'   Engineering Manuals.
Each synthesis  report presents  guidelines  in  one  specific  area addressed by
the  DMRP.   One of  these  reports (3)  represents the  final  DMRP  guidelines on
the management of disposal  areas to maximize their  service  lives through de-
watering/densifying   the  dredged  material.   As pointed  out  in  the  earlier
papers  (1,  2),  the  primary purpose of  densifying  the material  is to gain the
additional   capacity  of the  site that  would  have  been  otherwise occupied by
water.   Since  dewatering coarse-grained material  and  silts  of  low plasticity
yield  little  or no  additional  volume reduction of the  material, emphasis in
the  program was  placed  on  dewatering  fine-grained  material.    Although  the
specific purpose  of  dewatering  (in the DMRP context)  is  to reduce the volume
of and not to stabilize the material,  dewatering usually results  in the mater-
ial having greatly improved engineering properties  (e.g., higher  strength, low


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compressibility,  etc.)-   Consequently,  in  many cases,  dewatering/densifying
dredged material is synonymous with stabilizing the material.


                          GENERAL MANAGEMENT CONCEPTS

INTRODUCTION

     Most concepts involving long-term disposal site management will  result in
increased capital  construction  and  manpower/administrative  cost.   However, in
most instances,  the  unit  disposal  cost of operating  the  site  over the design
life will  be equal to or  lower than  cost for an  unplanned  operation.   Thus,
when incorporating  the  subsequently described procedures in an overall  plan,
the total cost, both short- and long-term, of concept implementation  should be
considered.

     Application  of  any  general concept  to  a given disposal  site is  a  site-
specific design  problem.   Whether  or  not any  concept will  prove  feasible can
only be  determined  after  careful  planning and study, not only of the concept
itself,  but  of  the alternatives to and constraints involved in concept imple-
mentation.

THIN LIFE PLACEMENT

     The most  economical  dewatering  mechanism is  Mother Nature,  through the
evaporative  process  (4).   The  rates  at which  various soils  will  dewater
through evaporation were studied in detail (5).  The depth to which a layer of
fine-grained dredged material  will  dewater  is a function of  the  net evapora-
tion at  the  site.   The  net evaporation is equal  to the  total  evaporation over
a  given  period  of  time minus  the  precipitation during that same  period.   In
many areas the net evaporation is small and in fact is negative in areas  where
precipitation  exceeds  evaporation.   The  latter condition  is  common  in  many
coastal areas.

     In  order  for  dredged  material  to dewater with no active dewatering  tech-
niques  applied,  the thickness  of  the lift  placed  in the containment  area in
general  should  not  exceed  the water loss available from about half of the net
evaporation  during  the period  from deposition to placement of the next  lift.
In some  areas  net evaporation available at particular  times  during  the  total
period  should  be considered.    For  instance  if  the lift is to remain  in the
disposal  area  for  one year before  another lift is  placed there may be several
months  where the net  evaporation is considerably greater than the average for
the entire year.  During this  time  a desiccation crust on fine-grained dredged
material  will  develop.  Once  a crust  forms,  subsequent  wetting will  not  cause
the crust  to revert  to  the original   near liquid  state.  Consequently,  there
may be  crust formation and thus dewatering/densification in  areas  where the
average net evaporation  is low or negative.

     It  is   recognized  that  in  most   instances  it  is  not  possible  to  place
dredged  material  in  extremely thin  lifts  because  of  the  limited  land  area
available  for  containing  relatively  large volumes  of  dredged material.   In
some cases the situation can be improved through such techniques as carefullly
selecting the time of year (maximum net evaporation) for placement, the use of


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compartments within the  area  to increase the length of time the material will
be  in  the area  prior  to placement  of  the next lift.  These  and  other tech-
niques are discussed  in  detail  in References 3 and 6.  In subsequent parts of
this paper methods  for  taking advantage of rates approaching the total evapo-
ration rate will be discussed.

OTHER MANAGEMENT CONCEPTS

     Thin lift placement of fine-grained dredged material  is the most economi-
cal management  scheme when  specific  site conditions prmit.   As man's input of
energy into the  system  increases,  costs also  increase.   As  part of the DMRP,
several  techniques  for  dewatering fine-grained  dredged material  were consid-
ered and evaluated to varying degrees.   The controlling factor in establishing
feasibility was almost always economics.  If the cost of dewatering the mater-
ial  exceeds  the  cost  of constructing  and using  a  new site,  the  dewatering
technique is in general  not feasible.  However, this is a site-specific factor
and what  is  not  economically feasible  in  one  area may be feasible in another
area.   In  some  instances,  environmental concerns  are  paramount  and costs are
secondary  to  assuring the  dredged  material  is contained in  a specific area.

     In  the  earlier papers  (References 1  and  2), the dewatering  techniques
being considered in the DMRP were discussed in some detail and indepth discus-
sion of  all  of  the techniques will  not be given here.  Techniques considered
were:

           1.   Progressive Trenching
           2.   Vacuum Wellpoints
           3.   Windmill  Power Feasibility of Vacuum Wellpoints
           4.   Sand Slurry Injection
           5.   Natural Freezing and Thawing
           6.   Mechanical Crust Stabilization
           7.   Underdrainage
           8.   Low Voltage Gradient Electro-Osmosis
           9.   Vegetation Dewatering
          10.   Capillary Wicks

     All of the techniques were successful  to varying degrees.  Details of the
various  studies  and results  are  presented  in  References 7  and  8.   The most
universally applicable  technique  appeared  to  be  progressive  trenching where
trenches  are  placed in  the fine-grained  dredged  material  to  rapidly remove
surface water plus increasing the effective evaporation rate.


                              EVAPORATION DRYING

     During the  early  phases  of the DMRP  it  was noted that a relatively thin
crust  usually developed  over the underlying  soft,  wet  fine-grained dredged
material  confined  to  a  disposal area.    It was  assumed that this crust devel-
oped and  retarded or  eliminated any further evaporative drying by sealing the
underlying material  from the  evaporative  processes.    It was noted, however,
that in  some  instances  the crust developed  to  relatively great depths and in
some cases the crust would be as much as 15 feet thick (9).
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     A close evaluation  of  the  site revealed that the confined disposal  areas
generally acted as  "bath tubs"  and water entering them  through  precipitation
or  other  sources  could  not be  removed except  through  evaporation.   It  was     ^
further noted that  in  areas where the net evaporation was  high  or where sur-     fl
face water was  allowed to drain  the crust thicknesses were much greater.   As a
result of  these observations an  extensive  study  of the mechanisms  of  crust
development were made (5).

     The laboratory  and  controlled  field studies (5) revealed that the  crust
in fine-grained dredged material  did not seal  off the underlying  soft  material
from the evaporative  process.  As the desiccation crust  develops,  cracks also
develop.   In most  cases  water would continue to  be  removed  from these cracks
by the evaporative  process  and  the cracks will  continue  to develop as long as
the  water  supplied by  capillarity  was less  than  the evaporative  demand.
Consequently,  the  desiccation cracks  can extend  to considerable depths  and
dewatering  of  the  fine-grained  dredged  material will also continue  to  these
depths.

     When fine-grained dredged material  is  placed hydraulically  in a  contain-
ment area approximately four volumes of make-up  water are required for a given
volume of i_n situ  sediment.   Most of this water is drawn off  the area through
some type of sluice.   In studies  of fine-grained  dredged material  exhibiting
various engineering  properties,  it  was found that after  the surface water was
removed cracks  would begin  to  develop  as  the  water content  of the  material
reached approximately  1.8 times  the  Atterberg   liquid limit  (LL)  (5).   This
condition is referred  to as the  "decant point."   The  1.8 LL  is  a statistical
average and of  course can vary from material  to  material.

     As the desiccation  cracks  develop  the  average water content of the  re-     I
suiting polygons was found to be  approximately 1.2 times  the Atterberg plastic
limit (PL).   Again, the 1.2 PL is  only a statistical  average and  may vary.   As
shown in Figure 1,  the volume reduction through  removal of water is linear and
the  slope   of  the   straight  line   is  the coefficient  of shrinkage,  C  .   The
relation  remains   linear until   the water  content  approaches  the  Atterberg
shrinkage limit  (SL).   The  desiccation  cracks   were  found to account  for as
much as 20 percent of the total  volume change.   The rate  of water loss through
evaporation was  found to  vary depending on whether the  dredged material  was
derived from marine  or freshwater sediments.   For marine or saltwater dredged
material  the estimated water loss  in  inches,  centimeters, etc.,  is  equal to
about  35  percent  of  the effective evaporation   rate while  for freshwater  the
loss is approximately  50 percent  of the effective evaporation rate.   In order
to  take  maximum advantage  of evaporative drying,  surface water  must  be  re-
moved.   This includes removal of  surface water that is held in the desiccation
cracks.  A  technique  for removing surface water was developed by the  DMRP and
will be discussed in detail  in this paper.


                             PROGRESSIVE TRENCHING

BASIC CONCEPT

     The desiccation cracks formed in fine-grained dredged material are inter-
connecting  and  thus a system of  trenches within a  disposal  area  will  remove


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             150
            100
          O
          ฃT
          UJ
             50
              0
                          I          I

                      BORING BI-3
                   2.5 TO 5.0 FT. DEPTH
                          I
                                           = 2.32
                20       40       60        80
                         PERCENT INITIAL VOLUME
100
Figure 1.  Typical   linear  shrinkage  curve  for  dredged  material  tested  (from
          Reference 4).
water  from both  the  surface  and  from  the  cracks  if  the flow "line  of  the
trenches is below the bottom of the cracks.   Since  the  material  underlying  the
crust  is  at or  above  its LL  a  trench much  deeper  than the crust  thickness
cannot  be  maintained.    Consequently,  as  the desiccation  cracks  deepen  the
trenches must also be progressively deepened to assure  the water in  the  cracks
will be drained.

     The progressive  trenching concept  lowers the  surface  elevation  of  the
dredged material  through  three mechanisms.   The  first  is through shrinkage of
the  upper  material  in the  crust.   Second, the progressive  lowering  of  the
perched water  table in  the  containment  area  increases  the effective  stress
acting on  the  soft underlying  dredged material thereby causing  it to consoli-
date.  The  third  mechanism  depends on the  foundation material and water table
conditions.  If  the foundation material  is relatively soft  and the perched
water  table connects with the  foundation water table,  the  increased effective
stresses from  lowering the  perched  water  table  will cause the  foundation  to
consolidate.

TRENCHING TECHNIQUES

     The major  problem associated with  the progressive trenching  concept  is
the construction of the trenches  themselves.  At  the  decant  point the material
is  too soft to  support  conventional equipment such as draglines.   Equipment
for  operation  in  disposal  areas  was evaluated as  part  of  the DMRP  (10). Only
one piece of equipment was found that could operate in  the  soft  dredged  mater-
ial  and  rapidly  produce  trenches.   The Riverine Utility Craft  or RUC (Figure
2)  was  found  to  be   suitable  if  not   ideal for  use.   The  RUC  produces
trenches with  the  tracks formed  by  the  rotors.   The RUC  was described  in
detail in an earlier paper (2).

     In many respects the RUC is  similar  in appearance  and  operational charac-
teristics  with  the Dutch-made Amphirol.   However, the RUC is  a much heavier
vehicle and the rotors are over three times larger, making  the RUC a much more
effective  trenching  tool.   The  Dutch use the Amphirol  in the  "ripening" proc-
                                       359

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ess  of  dredged  material  placed  in  polders  (11).   The ripening  process  is
similar to the progressive trenching technique.

     In the progressive trenching  technique initial shallow trenches are made
after the material  reaches  the decant point.   The  trenches  are progressively
deepened as required  with the RUC until  the trenches are about two feet deep,
the  limit  of  the  RUC's  effectiveness.    With  two  feet  of  crust  other more
conventional  equipment can  be selected using procedures outlined in Reference
10 to continue the deepening process.   Details of the trenching techniques are
given in Reference 3.

FIELD TESTS

     The progressive  trenching  technique  was  field  evaluated at  the  Upper
Polecat  Bay  (UPB)  disposal  site  in  Mobile,  Albania  (4).   The  85-acre site
filled with  8 to  12  feet  of fine-grained dredged  material was  described  in
Reference 2 along with the general  plan of tests.

     Computations were made  based  on  extensive data collected  at  UPB to pre-
dict the dredged  material  surface  settlement or volume gain in the site.  The
perched water  table at  the  UPB site did not connect with the foundation water
table.   Consequently  foundation consolidation was  not  considered  and because
of the soft nature of the  material, rebound of the foundation was not expected
and  did  not  occur  as the perched  water table was  lowered.   Containment area
volume gain was expected only from shrinkage of the crust and dredged material
consolidation.

     Average  data  used  to  predict  shrinkage and  consolidation are  shown  in
Figure 3.  The  settlement due to shrinkage was  determined  from the following
relationship:

                                   AH = Hr^                               (1)
                                          s

Where     AH  = Settlement  due to shrinkage.
           H  = Thickness of strata.
          Aw  = Average change in water content,  percent.
          C  = Coefficient of shrinkage.

Since the dredged  material  had been placed several  years  prior to initiating
dewatering,  the water content of the material  was at about its LL.   Also, data
indicated that  average water content  of the polygons would be about at the PL
(as  opposed  to  the  statistical  average   of 1.2  PL  discussed earlier).  Aw
was  then  taken to  be equal  to  LL-PL.   The  average C  was  2.34.   Predicted
shrinkage as  a function  of drawdown is shown in Figure 4.

     Conventional  theories   were  used  to  compute  expected  settlement from
consolidation  of  the  soft dredged material (4).   The  resulting consolidation
as a function of drawdown  is shown in Figure 5.   The coefficient of consolida-
tion  of  the  material was  computed  to  be 0.3  cm2/sec which  indicates that
dredged material consolidation would reach 90 percent of total  primary consol-
idation approximately two  months following  imposition of load.
                                      361

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     Total predicted  settlement is  shown  in Figure 6.  Because  of  the rela-
tively short time  required  for the material to  consolidate,  total  settlement
was  the  sum of  that from  shrinkage  and consolidation  at a  given  drawdown.
Field data (also plotted on Figure 6) show that the predicted settlements were
less  than  those observed in  the  field.   The difference in  the  predicted and
observed behavior was not great and the predicted values were on the conserva-
tive side.  Therefore, the analytical technique appears acceptable.

PREDICTION EQUATIONS
     The following equations have been developed to predict dewatering effects
once  the  dredged  material  has  reached  the  decant  point.   The  approximate
thickness,  in  feet,  of dredged material  at  the end of the  decant  phase
when surface drainage improvement should be initiated, is  given by
                                                                 H
                                                                  dm'
                     dm
                             cs
% sand
100

•["
43
% sand\
100 ;
,560Ads
w ,-i
cd
WcsJ

                                                                           (2)
where
 V   = volume of channel  sediment to be dredged,  cu yd.
sana = percentage of sand in the channel  sediment.
 w  , = average water content of the dredged material  at the end of
       the decant phase,  percent.
          w
           ,cs
     = average water content of the channel  sediment,  percent.
          A ,  = area of the disposal site, acres.

In lieu  of  better  data,  especially if the calculation is made prior to dredg-
ing,  w  , may be taken at 1.8 x LL, and Equation 2 may be written as
                                                                           (3)
Effect of evaporative dewatering

     The  estimated  water loss,  in  inches, from evaporative  dewatering AW is
given by the relationship
u - p7\/
dm cs
% sand
100
/1 % sand^
[(1 100 '
1.8 LL
w
cs J
43.560A
ds
                                       0.35Ep

for saltwater dredged material and by

                                   AW = 0.50Er
                                                                  (4)
                                                                  (5)
for freshwater  dredged  material,  where Ep is the Class A Pan Evaporation (see
Reference 3) for the dewatering interval.

     The depth,  in  inches,  to which the initial thickness of dredged material
will be dewatered H. is given by
                                     364

-------
                       AVERAGE FIELD SETTLEMENT
                       STA. 10 + 00 to 24+00
                               PREDICTED SETTLEMENT
                                            I
                      I           2          3
                           DRAWDOWN IN FEET
      Figure 6.   Potential  settlement  versus drawdown and  field results.
                       w
 H.  =
                       w
                        cr
                            AW
                             cr
                         O.Olw
                             cd  s
                                                                    (6)
where     w   =  average water content of the dewatered dredged material
          cr
               (crust),  percent.
          G  -  specific  gravity of  the channel sediment/dredged material
               sol ids.
In the absence  of better data, w ,  may
assumed as 1.2  x PL.   In such a case,
      be assumed as 1.8  x LL, while wrio may be
     Equation 6 becomes
                                              cr
H-l-5^
                                AW
(1.5^ - 1)
             (1
                                              0.018LLG2
                                                                    (7)
                                  365

-------
     Vertical   subsidence,  in  inches  of  the dredged  material  surface H   is
computed as
                                 HS =
                                        AW
                                           dc
                                          100
                                                                           (8)
where P ,   is  the  percentage  of total  dewatering volume gain due to the vol
of the  space  between  desiccation  cracks.   In lieu of  better data, P^ may
taken as 20 percent, and Equation  8 becomes
                                                                           ume
                                                                     dc may be
                                   M  — *-*"
                                   Hs ~ T72

     The crust thickness,  in inches, formed by desiccation H   is  given by

                                 H   = H.  - H                             (10)
                                  cr    i     s                            ^  /

     The estimated  volume  gain,  in  cubic yards, from  evaporative  dewatering
shrinkage V  , is computed by
                       u   - A  AW
                        gd " AdsAW
                                                43>560
                                         100  '  12(27)

Effect of increase effective stress consolidation
                                                                          (11)
P —

Gs(l
1 +
+0.01wcd)
O.Olw ,G
cd s
* k - H.
*w / dm i
12 I 2 "i
     The average initial  effective  stress,  in pounds (force)  per square foot,
at  the  center  of  the  undewatered  dredged  material  (subcrust)  layer  P.  is
estimated as                                                              ]
                                                                          (12)
where y  is the unit weight of sale or freshwater,  in pounds (force) per cubic
foot.   In  lieu  of  better data,  w  , may be taken as 1.8 x LL,  and Equation 12
becomes
                                                                          (13)
     The increase in effective stress,  in pounds (force) per square foot,  from
water table lowering Ap is approximated by

                                   Ap = HiYw                              (14)

     The  approximate  consolidation  settlement,   in  inches,  resulting  from
increased effective H  is approximated by
D —
r -
G (1 + 0.018LL)
s 1
1 + 0.018LLG
Yw fdm • Hi ,
12 I 2 Hi
                                  - VCc
                         c   1  + 0.01wcdGs
                                            log
                                                                          (15)
                                     366

-------
where C   is the  compression  index  for the dredged material.   If  better data
are  notc available,  w  .  may  be  taken as  1.8  x  LL,  and Equation  15  becomes

                             (Hdm -  H.)CC      p. + Ap
                        Hc = 1 + 0.018LLG  log — -                    (16)
                                         s
     Additional disposal volume gain, in cubic yards, from subcrust consolida-
tion V   is computed from
                           -HA   n - % sancS 43,560
                        gc    cAds (1   ~~m') T2(27)
     Total  settlement,  in inches,  of the  dredged  material  surface  from  de-
watering H, is thus

                                 H.  = H  + H                              (18)
                                  t    s    c                                '
     Total  disposal  area  volume gain, in cubic yards,  from  dewatering V .  is
given as                                                                 ^

                                V   = V   + V                             (19s)
                                 gt    gd   V                           v'y;
     The  thickness,  in inches,  of  subcrust  remaining  to be  dewatered  H   is
given by

                              H  = H .  - H- - H                           (20)
                               r    dm    i    c                          v   '
     The volume, in cubic yards, of dredged material available for removal  and
productive  use V  is estimated as
                p    ds
                                     sand,"! ,  ,,   % sand
cr v'     100  '     dm  100
]•
                   H
43,560
12(27)
                                                                          ,_.
                                                                          uu
     More  detailed  information on  the use  of  these equations  and  other re-
quired computation  is  given in Reference 3  which  also  contains example prob-
lems.  A computer program has been developed to assist with the analyses (12).


                                    SUMMARY

     The proper management of disposal areas can increase the service lives of
areas  containing  fine-grained dredged material.   Guidelines  have  been  devel-
oped during the DMRP to aid in developing management plans (3, 13).  Work will
continue  under  the  Corps of Engineers1 Dredging  Operations  Technical  Support
program to verify and refine the methodologies.


                                  REFERENCES

 1.  Calhoun,  C.  C. ,  Jr.   "Dredged  Material  Densification   and Treatment of
     Contaminated Dredged Material," Management of Bottom Sediments Containing
     Toxic Substances  -  Proceedings  of the Second U.S.-Japan Experts Meeting,


                                     367

-------
     October 1976,  Tokyo,  Japan.   hPA  hcological  Research  Series  600/3-77-U83,
     July  1977,  EPA  Environmental  Research  Laboratory,  Corvallis,  Oregon.

 2.   Calhoun,  C.  C.,  Jr.   "Densification,  Treatment,  and Management  of  Dredged
     Material  Disposal  Areas,"  Management  of  Bottom  Sediments  Containing  Toxic
     Substances  - Proceedings  of  the  Third U.S.-Japan Experts Meeting,  Novem-
     1977,   Tokyo,  Japan.   EPA Ecological Research  Series  600/3-78-084,  EPA
     Environmental  Research  Laboratory,  Corvallis, Oregon.

 3.   Haliburton,  T.  A.   "Guidelines for  Dewatering/Densifying  Confined  Dredged
     Material,"  Technical  Report DS-78-11, September  1978,  U.S.  Army Engineer
     Waterways Experiment  Station,  Vicksburg,  Mississippi.

 4.   Palermo,  M.  R.   "An  Evaluation  of Progressive Trenching as a  Technique
     for  Dewatering  Fine-Grained  Dredged   Material,"   Miscellaneous  Paper
     D-77-4, December  1977,  U.S.  Army Engineer Waterways Experiment Station,
     Vicksburg, Mississippi.

 5.   Brown,  K. W. ,  and Thompson,  L.  J.   "Feasibility Study of  General  Crust
     Management  as  a Technique  for Increasing  Capacity  of Dredged Material
     Containment  Areas,"  Technical  Report D-77-17,  October 1977, prepared  by
     Texas   A&M  Research  Foundation,  Texas  A&M  University, College Station,
     Texas,  for  the Environmental  Laboratory,  U.S.  Army  Engineer  Waterways
     Experiment Station, Vicksburg,  Mississippi.

 6.   Bartos,  M.  J. ,  Jr.    "Containment Area  Management  to  Promote  Natural
     Dewatering  of  Fine-Grained Dredged Material,"   Technical  Report D-77-19,
     October  1977,   Environmental  Laboratory,  U.S.   Army  Engineer  Waterways
     Experiment Station, Vicksburg,  Mississippi.

 7.   Haliburton,  T.  A.  "Dredged  Material Dewatering Field Demonstrations  at
     Upper   Polecat Bay  Disposal  Area,  Mobile, Alabama,"  Technical  Report  (in
     press),  U.S.   Army  Engineer  Waterways  Experiment   Station,  Vicksburg,
     Mi ssissippi.

 8.   Chamberlain,  D. J. ,  and  Blouin,  S.  E.   "Freeze-Thaw  Enhancement of  the
     Drainage  and  Consolidation  of Fine-Grained Dredged  Material in Confined
     Disposal  Areas,"  Technical  Report D-77-16,  October  1977,  prepared  by
     Foundations  and  Materials Research  Branch,  U.S. Army Cold Regions  Re-
     search and  Engineering  Laboratory, Hanover, New Hampshire, for  the  En-
     vironmental  Laboratory,  U.S.  Army  Engineer  Waterways  Experiment Station,
     Vicksburg, Mississippi.

 9.   Johnson,  S.  J.  e_t al.    "State-of-the-Art Applicability  of Conventional
     Densification  Techniques  to  Increase  Disposal  Area   Storage  Capacity,"
     Technical Report   D-77-4  (Appendices  A-C  on   microfiche),  April  1977,
     prepared  by  the Soils and Pavements  Laboratory for Environmental  Labora-
     tory,  U.S. Army Engineer Waterways  Experiment Station,  Vicksburg,  Missis-
     sippi.

10.   Willoughby,  W.  E.   "Assessment of Low-Ground-Pressure  Vehicles  for Use  in
     Containment  Area  Operations  and Maintenance,"  Technical Report  D-78-9,
     July 1978,  U.S.  Army Engineer  Waterways Experiment Station,  Vicksburg,
     Mississippi.

                                     368

-------
11.   Adriaan Volker Dredging Company.   "European  Dredging Practices," Techni-
     cal  Report  (in press),  U.S.  Army Engineer Waterways  Experiment  Station,
     Vicksburg,  Mississippi.

12.   Hayden, M.   L.  "Prediction  of  Volumetric Requirements for Dredged Mater-
     ial  Containment Areas," Technical  Report D-78-41,  August 1978,  U.S.  Army
     Engineer Waterways Experiment Station,  Vicksburg,  Mississippi.

13.   Montgomery,   R.  L.  et  _a11.   "Guidelines  for  Designing,  Operating,  and
     Managing Dredged  Material  Containment Areas," Technical  Report  DS-78-10
     (in  press),  U.S.  Army Engineer Waterways Experiment  Station,  Vicksburg,
     Mississippi.
                                     369

-------
      IMPACTS OF OIL SPILL  AND  CLEAN-UP  ON THE EUROPEAN COAST:   AMOCO CADIZ

                                 William  P.  Davis
                        Chief,  Bears  Bluff Field Station
                  Gulf Breeze Environmental  Research Laboratory
                      U.S.  Environmental  Protection Agency
                              Wadmalaw Island, S.C.
                                   INTRODUCTION
      Accidental  release  of  petroleum
 transport  or transfer  from ships will
 pollution  control   and  abatement efforts.
 Amoco  Cadiz wreck  on  the  Brittany  coast  of
              spill  resulting  from man's
or  other  hazardous  substances  during
continue to  be  a major focal  point  of
     At the  time of  this writing  the
      France  (Figure 1) represents
 actitivies.   It occurred  on  one of
the
the
and
for
largest oil
world's most  productive  sea  coasts in  a  nation where both  technological
scientific  skills  abound.  Heavy  weather contributed  to both  the  causes
the wreck  and  the  subsequent  spread of  the  petroleum to  over 200 linear kilo-
meters  of  biologically  rich,  high energy coastal habitats.   From  the moment
the French realized the  existence  of the impending disaster there was a public
mobilization of  fishermen,  farmers, students,  scientists,  and clean-up equip-
ment; all  attempting  to take  action  appropriate to  prepare  for the coming of
the "black tide"  or "maree noire".

     This  report  attempts  to  summarize  highlights  of impacts,  ecological
effects, and evolving response efforts  of interest to  persons living or work-
ing along the shores of the world's oceans.   LESSEPTIUES
                 KERLOUAN
        PORTSALL.
ILE d'OUESSANT


      LE CONOUET


PTE. deST MATHIEU
                             PUXJESCAT
                  A4LABER WRAC'H
                 L'ABER BENOIT

               COB-CNEXO
                     BREST
                             Coast of Brittany, showing location
                             of spilled oil  (from Hess, 1978).
                                       371

-------
                            CHRONOLOGY OF SPILL EVENTS
      The Amoco  Cadiz (Figure  2)  hit rocks one mile  (1.6  km)  offshore from  the
 town of  Portsall,  France on  16 March 1978.  The ship's  steerage had been lost
 and attempts  to pull  her from the  rocks failed as  several tow  lines parted.
 Winds of 40-50  knots contributed  to these failures; within six hours the ship
 began breaking  up,  resulting  in  the release  of  216,000 tons of  Iranian  and
 Arabian  light crude oil, plus  4,000 tons  of  fuel  into  the ocean.   During  the
 next  week   heavy  seas   emulsified  the   escaping  petroleum  into  a  stinking
 'mousse" and  spread the  spill  over 200  kilometers  of  the   Brittany  coast.
                                                                 ฃf
                            1,095.91  FT.-
                            BREAK
          BREAK
      REGISTRY MONROVIA LIBERIA
      OWNER AMOCO TRANSPORT CO
      CAU/OFF Nฐ A8AN/4773
      POWER 2SA 8CYL DIESEL , 980mm * 2.000mm
      22,678Kw/30,400 BMP (SINGLE SCREW)
      SPEED 15 25 KTS
      MAX DRAFT 65 FT /19 8] M
      CAPACITY 233,690 DWT
            109,700 GRT
            91,000 NET/TONS


      ABOVE DATA PER LLOYDS REGISTER
  TANK LAYOUT AND VESSEL
DRAWINGS NOT AVAILABLE
        Figure  2.   General  layout and dimensions  of Amoco Cadiz showing
                    locations of breaks (from  Hann et aj. , 1978).


     Geologically,  the  Brittany  coast  is a  shield  shoreline,  underlain  by
igneous and  metamorphic  rock  complexes,  with  headlands,  crenulate bays,  small
and  large  beaches,  rocky  islands,  tidal flats,   marshes,  all  representing
widely varied ecological  habitats.   Although  no major rivers enter the area,  a
number of "abers"  or  small  rivers are found.   Initially,  wind moved the petro-
leum  in   an  easterly  direction  piling  oil  up against  every  westward facing
coastal feature, or concentrated it into estuaries  with westward facing mouths
or  entrances.    These westerly winter winds   are part of  the  annual  weather
pattern for this part  of  the ocean,  Manche, also  known as the English Channel.
                                       372

-------
     In  early  April  winds  typically  swing  around and  become  northeasterly.
The shift  in wind  direction occurred  about  3-4  April,  1978 (Figures 3a,b and
4a, b).   The  shift -redistributed  much petroleum  to  previously  shielded sec-
tions of the Brittany coast.

     In addition,  the  highest  spring tides of the season (9-meter tide range)
occurred within  the  two-week  span  after the wreck (Figure  5).   This resulted
in wide  exposure  of  coastal  intertidal habitats  to  oil,  necessitating con-
siderable  ingenuity  by the people of  Brittany  in attempting to  clean their
impacted coast.

     The Ministry  of  Interior  and  the French Navy directed much  of the effort
to disperse oil  at sea with chemical  agents.  Little  information is available
on just  what  chemical dispersants  were employed,  where they were  used or in
what quantities.   Apparently over  50 tons  of dispersants were sprayed during
18-22 March.  Four ships  were  observed spraying sheen,  not mousse, on 8 April
1978.   These ships had been making daily sorties since  18 March  from the port
of Brest,  France.   Interviews  with petroleum company officials  revealed that
at least  four  different  chemical  agents, plus chalk, had  been  applied but no
useful  documentation  was available.

     The NOAA/EPA  Special Report:   "The Amoco Cadiz Oil Spill -  A Preliminary
Scientific Report"  (Hess,  1978) provides a valuable summary of initial events,
responses  and  assessment  of the spill.  Subsequently,  a French-United States
special  commission has been  established,  co-chaired  by Dr. Lucien Laubier,
Director of Centre  Oceanologique de Bretagne (COB) of  the Centre  National pout
I1Exploration   des  Oceans  (CNEXO),  and Dr.   Wilmot N.   Hess,  Director of NOAA
Environmental   Research Laboratories  (ERL).   This  commission meets  each six
months to review scientific  activities for assessing effects of  the spill, and
to award  funds  for specific research grants to consider the long-term effects
of petroleum from the spill.

     Oil spills  are  a challenge to pollution-oriented  ecologists.  Even after
a  number  of   international  symposia  which  have  produced   extensive  reports
(Bates,  1978),  one gets  the  impression that the  ecologist faces  a desperate
struggle when  oil  spill  catastrophes occur.  The  magnitude  of  these events,
particularly from  ships the size  of Amoco Cadiz is simply beyond the scale of
experience of most scientists and planners.  Furthermore, the emergency atmos-
phere surrounding  clean-up  operations has  rarely  incorporated much considera-
tion or  realization  of need  for scientific assessment.  The Amoco Cadiz oil
spill  has  spurred  efforts in  the United States  to initiate ecological impact
assessment  combining  physical  oceanography,  coastal  dynamics,   and  habitat
assessment, ecological/behavioral  effects  with chemical  analyses.  Multina-
tional   teams  brought together  in  Brittany  by  the Amoco Cadiz  incident have
been developing  and  exchanging  newly created ideas (Conan et al.  1978), tech-
niques and strategies to use scientific methods for impact assessment, estima-
tion of  damage  to marine ecosystems  and  eventually,   procedures  for habitat
restoration.

     Events following  the Amoco Cadiz oil  spill  have  provided  quantities of
material  for  the press,   sociologists,  economic  strategists,  and politicians.
With regard to  the  ecology, the assessment of  effects still continues.


                                     373

-------
                                                   SECTION H
                          vWRECK SITE
                      KERSAINT
                                 Awc-2        FIRST STUDY PERIOD
                                'PORTSALL
                                 •AMC-I       -----Area Exposed at Low Tide

                                            0               2km
Figure 3a.   Locations of observation stations  in  Section  II, the Portsall area,
            during the first study period (March  19  to  April 2).  Heavy oil
            accumulations are indicated by the dark-stippled pattern.
                                                    SECTION  II
                           WRECK SITE
                                            SECOND STUDY PERIOD J
                                 jPORTSALL                        f
                                 AMC"'  	..--• Area Exposed at Low Tide   ~N~

                                            0               2km    II
                     KERSAINT
Figure  3b.   Oil distribution for Section II  for  second  study session, April 20
            to 28.  Heavy and light oil  coverage are  indicated by the plus and
            light-dot patterns, respectively (from  Gundlach and Hayes, 1978).
                                   374

-------
                                .. -. .^PRIMEL TREGASTEL
      147
             •   />~CD':- n
             , .  /I3l2n x-*;  < \i
                                            FIRST STUDY PERIOD

                                             0    24    6km
                                MORLAIX
Figure  4a.   Location of stations in Section VII,  Roscoff to Pointe de Plestin
            (F-142).  Oil distribution during the first study session, March
            19  to April 2, is indicated by the dark-stippled pattern.
     147'
                                    PRIMELTREGASTEL
                                          SECOND STUDY PERIOD

                                              024   6km
                                                                  -N-
   Figure 4b.   Oil  distribution along the coastline of Section VII during
               the  second study session, April  20-28.   Heavy ana  light oil
               coverage are indicated by the plus and  light-dot patterns,
               respectively  (Gundlach  and  Hayes,  1978).
                                   375

-------
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                                                    376

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                         BIOLOGICAL-ECOLOGICAL EFFECTS

     Initially,  some  4000  or more birds perished,  including  puffins,  guille-
mots,  and  razorbill  auks  which  are  considered  endangered  species  in  this
region.  Additionally,  cormorant  species  (shag),  loons and  other  migrating
diving birds  were severely  affected.  Certain  intertidal  organisms  including
species of molluscs,  echinoderms,  crabs, worms,  algae,  Crustacea,  and fishes
were also  killed.

     In one case,  oil  contamination  of the shoreline caused mass death of sea
urchins (Echinocardium)  and  several  associated species  of  molluscs.   In  this
particular situation  it  was  evident  that organisms which are normally burrow-
ing  forms  had  surfaced,  apparently  driven  from  the substrate  by  petroleum
components which  penetrated up  to  30  cm  into  the  sandy bottom  habitats.
Whether this  event is related to use  of dispersants or storm-induced mixing of
seawater,  sediment and petroleum is not yet  understood.

     Bretagne benthic organisms  have  been  studied for a number of years.   The
amphipod  crustaceans  comprise  90% of the  species  diversity  and 40%  of  the
biomass  in  fine  sediments.   Normally  amphipods   are present  in numbers  of
15,000/m2  in summer, and 8,000/m2 in winter.  Within a fortnight of the wreck,
the population dropped  to  2-5/m2,  the number of species from the normal 23 to
only 7 (Cabioch,  personal  communication; NOVA,  1979).  These organisms repre-
sent the  principal  food for commercial  fishes  including sole,  sea  bream and
others.  Molluscs and polychaete  worms at these  particular  stations  were not
so dramatically affected.

     A calcareous algae,  Lithothamnion,  forms  "brush"  piles,  or areas  with
high amounts of interstitial  space.  Such habitats have become benthic entrap-
ments  for  oil-sediment  mixtures.   This  phenomenon  has  not been extensively
studied and  needs  careful  evaluation to  determine  potential  ecological  im-
pacts.

     Dr.  Claude Chasse'  has  conducted  extensive benthic biological surveys at
Morlaix,  and  other bays including the Bay of Lannion,  where  in  the aformen-
tioned example  early effects of  oil  and/or  dispersants to  benthic  organisms
was most dramatic.  His  research  (Chasse',  1972)  spans  ten years of study of
the macrobenthos  between St.  Efflam and Michel-en-Greve.   At this site, 3-7 km
of beach were covered with  five  windrows  of sea  urchins,  razor clams  and other
organisms.   Continuation  of  ecological  assessments at this   site,  Lannion,
Morlaix,   and  others  are  of  extreme  importance  to  better understanding  of
long-term  effects of petroleum on benthic  organisms.

     Through   the  University  of  West  Brittany, students were  organized  into
survey  cadres.    During  initial  phases  of  the  spill  some 150-200  students
visited intertidal areas (during  low spring  tide) and counted  benthic organ-
isms using printed survey sheets.  These  sheets  were collected and compiled by
Drs. Chasse' and  Glemarec.   More  than  600 students took part in repeating the
"body  counts" of  dead organisms.   The  results of these  repetitive visits and
subsequent assessment of benthic  populations will be invaluable to ecological
comprehension of oil-organism interactions and mechanisms.
                                     377

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        FIRST TWO  WEEKS
        OIL TRANSPORT
     WIND _,
                      v heavny
                       oiled
                       headlands
        AFTER ONE  MONTH

                 WIND
Figure 6.   (Top) Oil pushed by strong
           westerly winds during the
           first two weeks was mainly
           deposited along westerly-
           facing  headland areas.
           Interior embayments gen-
           erally  remained free of oil.
           (Bottom) A wind shift during
           the  beginning of April
           spread  a light layer of oil
           deep into the embayments.
           Previously deposited oil
           along the exposed headlands
           was  greatly  reduced in quan-
           tity (Gundlach and Hayes,
           1978).
    WIND
                 ROCKY
                    HEADLAND
           CRENULATE BAYS
                                                       WAVES
                                                                   .LONGSHORE
                                                                   TRANSPORT
                  dunes
Figure  7a.   Entrapment of oil by
            crenulate bays.   Gener-
            ally, the southerly
            section of each bay
            remained free of oil.
  Figure 7b.   Illustration  of  the
              tombolo effect causing
              localized oil  deposition
              behind offshore  rocks
              (Gundlach and Hayes,  1978).
                                    378

-------
     Many small marsh  areas  were impacted, but the one surrounding the embay-
ment  south  of Isle  Grande  represents one of the  most heavily damaged.   Here
the configuration of  the  coast entrapped oil and  winds-forced the oil onto a
Juneus and Spartina marsh (Figures 6 and 7).  Oil depth over the marsh surface
varied with  specific circumstances,  but was  as  deep as 15 cm  in  some areas.
Effects on biota  were devastating;  polychaetes and other mobile invertebrates
littered isolated pools of water by the thousands.

     Clean-up of  marsh areas was given high  priority.  However, use  of  heavy
equipment without restriction  to single-access  work paths further  contributed
to destruction of the soils  and additional  disruption  of  the  habitat.  Rela-
tive  effects  of   oil  versus  clean-up activities will  be  difficult  to assess.
The area poses considerable challenge to planners  interested  in restoration.

     The emotional  impact of  any  oil  spill  is  symbolized by  the  tragedy  of
wild bird deaths.   In  the  case of Amoco Cadiz,  the  eastward  extension of the
spill  lashed  Les  Sept  lies (Seizh Enez) (Figure 8) which represents the south-
ernmost  nesting   colony  of  the  common  puffin,  an  endangered  species.   The
observation team  was  escorted to  the sanctuary on  2  April by ornithologists
from the Ligue Francaise pour  la Protection des Oiseaux (LPO).   At  sites  where
one would normally see approximately 300 pairs of puffins in prenesting court-
ship,  only one bird was found.  By 14 April "bird hospitals" had recorded over
850 puffin carcasses.  Spring migration was still underway so  the total impact
of oil  on  the Sept Isles colony  is  unclear.  Other  bird  species  using this
sanctuary include razorbills (100 pairs),  guillemots  (300  pairs),  kittiwakes
(100 pairs),  storm  petrels,  herring, greater- and lesser- black-backed gulls,
fulmars (100 pairs)  and gannets (4,000 pairs).


              SEIZH ENEZ                             *  "'   ;
              (LES SEPT ILES)                         I        ECHtLLA
                     ILE PLATE
                                  AUX MOINES
                       CERFS

      Figure 8.   Islands constituting Les Sept lies (from Milon,  1972).

     The species most  affected  by oil were diving birds (puffins,  razorbills,
cormorants, loons);  soaring and  far-flying  species (gulls, gannets)  had  far
fewer  immediate  deaths.   The  word  immediate is  emphasized  to denote  acute
toxicity.   In the case of gulls, these birds were observed feeding  on weakened
molluscs,  crabs, and worms.  Gannets  were  seen carrying seaweed  back to  their


                                     379

-------
nesting  sites  from areas  affected by  oil  slicks.   It  is  not  known  whether
contaminated seaweed  can cause  the  kind of  mortality which  has  been demon-
strated experimentally with  duck eggs  (Albers,  1977) or gull  eggs (Patten and
Patten, 1977).   By 2 April, three dead gray seals had been recovered from this
area of the Brittany coast.

     The  impact  on birds  was  noted to  be  "less than  expected"  by personnel
working  for  LPO  and  Societe pour 1'Etude  et la Protection  de  la  Nature in
Bretagne  (SEPNB).   This  observation  reflects  the  important  role  of specific
circumstances.   Did many birds  avoid this spill  because it was so massive and
contained  highly  aromatic  petroleum  components?   Were  migration  patterns
sufficiently different  during  this  year  (compared to  Torrey  Canyon)?   Had
populations  (as  known for  puffins,  razorbills,  and guillemots)  already been
decreased  by the Torrey Canyon  spill,  so  there were  fewer  birds  to  be af-
fected?   Answers to  these  questions  will depend on  research and better under-
standing, evaluation and knowledge of population dynamics.


                           FISHERIES AND MARICULTURE

     Husbandry and harvesting of the sea is as traditional  as farming the land
in Brittany.   Coastal waters of the North coast affected by the spill  support
a traditional  artisan seaweed  industry.   Many species of  algae are harvested
and  commercially processed  to  produce  alginates  for food,  soap  and  other
products.  Other algae,  as well as the Laminaria, are harvested by hand (up to
6-7 thousand metric dry  tons/year) and used as a supplement to livestock food.

     Much  of the contaminated  algae was removed during  clean-up activities,
since  these  plants  acted as natural  mops for intertidal oil.   The impact upon
the algae  industry cannot be assessed with the present data, although harvest-
ing  was  being  carried  out during the  summer of 1978.   It initially  appears
that washing by sea action prevented much of the damage.

     Rearing of  oysters  (Crassostrea gigas  and Qstrea edulis) is an important
industry  in Brittany.   A  valiant effort was  initiated at  the onset  of the
spill  to  place numbers  of oyster  racks  in  estuaries southwest of the antici-
pated  trajectory of  the  floating oil.    Of  course there was insufficient time
to remove all  the  racks.   Total assessment of  the  impact of oil pollution on
oysters is not yet available.

     Certain oyster  culture areas  of  Brittany  had initially been considered
"spared"  from  the  fate  suffered by such westward facing bays as Aber Wrach or
Aber  Benoit.   Later,  Morlaix oysters became  petroleum tainted and considered
unfit  to  eat,  even though the surface mousse never came to that area.

     Mussel  culture  is  also practiced,  but the effects of the Amoco Cadiz oil
spill  have  not  yet  been  assessed.    Part  of the  problem  is  related  to the
distribution and effects  of  the oil-sediment mixture which  has  been trans-
ported  by tidal  currents  to areas not  significantly  impacted by the  surface
mousse  (e.g.,  Morlaix).    The  benthic oil  poses particular  threats to crab,
scallop,  and commercial  fish species,  emphasizing  the need for comprehensive
chemical-ecological  studies of the food webs of coastal  fishery populations.


                                      380

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Another issue  is  whether traditional  fishery population  study  techniques  can
adequately discern  effects  of a  massive  pollution event such as  a  major  oil
spill.   One gets the impression,  from both the literature and from discussions
with statisticians, that  present  methodology does not yet meet these kinds of
ecoloqical assessment  needs.


                                  AGRICULTURE

     Another  impact which emphasizes  the environmental  interrelationship  of
sea, atmosphere,  and  land is  the unassessed  effect  of  airborne  contaminants.
On Easter morning,  the  stench of petroleum was evident 10-20 km downwind from
the coast  with the onshore  winds blowing  at 40-50  knots.   Fields  rich with
spring crops,  including  mustard  greens, broccoli  and  cauliflower  extended to
the edge  of  the  rocky  coast and  it  was apparent that  fields  were  "browned"
from petroleum-laden  mist blown  in  from the  stormy seas.   It  is  hoped that
studies were  made  to assess the impact  on this link in the food chain.


                  VULNERABILITY OF BRITTANY COASTAL HABITATS

     On the basis of experience in the study of earlier petroleum spill,  i.e.,
Metu1 a (Straits of  Magellan)  and  Urquiola (Spain),  Gundlach  and  Hayes  (1978)
and Gundlach  (1979)  have classified  coastal  habitats  into  a  vulnerability
index   designed to  predict  longevity  of oil  in  specific  habitats.  In this
system, on the scale  of  1 to 10,  the greater the value, the greater the  like-
lihood of long term damage.   Table  1, taken  directly  from  Gundlach  and  Hayes
(1978), includes comments  addressing the situation one month  after the wreck.


                         OIL SPILL CLEAN-UP ACTIVITIES

     In June,   1977,  legislation  had  been  adopted  in  France to  prevent  and
control marine pollution  from accidents or  releases  of  pollutants.   The plan
had become   known  as  "Plan  POLMAR"   (from  "plan  contra  pollution  marin").
Authority from the government of France flows from the national to local  level
via bureaucratic  networks.  Control  of pollution was conceived by "Ministry of
the Quality  of Life", but  executed  under  "Direction of  Equipment"  which is
comparable to  Departments of  Public  Works  or  Corps of  Engineers as far  as
operational   aspects are  concerned.   Enforcement authority was retained  by the
Ministry of  the Interior.  The first major spill to test Plan POLMAR was  Amoco
Cadiz.   The  maritime prefect  at  Brest was placed in charge of POLMAR; but the
operational   approach was  split  into  marine and coastline responsibilities due
to the  "two fronts" requiring action.

     Hann e_t al. (1978) summarized the first two months of clean-up activities
directed  at  Amoco Cadiz  petroleum.   Probably no other  spill  has  received so
thorough a clean-up, nor been so completely assessed (Figure 9,10 and Appendix).

     Over 5,000 French troops  were  mobilized for shoreline clean-up.  Because
of the  Easter holidays  thousands  of students  on  spring vacation  volunteered
for clean-up  and  ecological  survey  teams;  engineer (road  and  construction)


                                    381

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          TABLE  1.   THE OIL SPILL VULNERABILITY  INDEX WITH  PARTICULAR
                    REFERENCE  TO THE AMOCO  CADIZ OIL SPILL1
Vulner-
ab i 1 i ty
Index
    Shoreline Type;  Example
                                                        Comments
         Exposed  rocky  headlands;
         Douarnenez  to  Pte.  du  Raz  and
         Primel-Tregastel  to Locquirec

         Eroding  wave-cut  platforms;
         south  of Portsall  and  F-l  to
         F-82

         Fine-grained sand beaches;
         stations south of Roscoff
         (AMC-9 and  10) and east  of
         Portsall  (AMC-5)

         Coarse-grained sand beaches;
         AMC-stations 4 (near Portsall)
         and  12 (St. Cava) and  F-38

         Exposed,  compacted tidal  flats;
         La Greve de St. Michel
         Mixed  sand and  gravel  beaches;
         no really good  example of  this
         beach  type
         Gravel  beaches;  stations  F-ฃ
         95 and  129,  also AMC-16
         Sheltered rocky coasts;  common
         throughout the  study area
  9      Sheltered tidal  flats;  behind
         lie  Grande and at  Castel  Meur
  10
Salt marshes,  lie Grande marsh
                                 Wave  reflection  kept  most  of  the  oil
                                 offshore;  no  clean-up was  needed.
                                 Exposed  to  high  wave  energy;  initial
                                 oiling was  removed  within  10  days.
                                 All  only  lightly  oil-covered  after
                                 one  month,  mainly by new oil  swashes.
                                 Oil  coverage  and burial  after one
                                 month  remained at moderate  levels.
                                          No oil remained on the sand flat but
                                          did cause the enormous mortality of
                                          urchins and bivalves.

                                          The index value is due to rapid oil
                                          burial and penetration; all areas
                                          had compacted subsurface which
                                          inhibited both actions.

                                          Oil penetrated deeply (30 cm) into
                                          the sediment; clean-up by use of
                                          tractors to push gravel into surf
                                          zone seemed effective and not
                                          damaging to the beach.

                                          Thick pools of oil accumulated in
                                          these areas of reduced wave action;
                                          clean-up by hand and high pressure
                                          hoses removed some of the oil (this
                                          process is valid in non-biologically
                                          active areas).

                                          Tidal flats were heavily oiled;
                                          clean-up activities removed major
                                          oil accumulations but left remain-
                                          ing oil deeply churned into the
                                          sediment; biological recovery has
                                          yet to be determined.

                                          Extremely heavily oiled with up to
                                          15 cm of pooled oil on the marsh
                                          surface; clean-up activities removed
                                          the thick oil accumulations but also
                                          trampled much of the area; biological
                                          recovery has yet to be determined.
1  Higher index  values  indicate  greater long-term  damage  by  the  spi1!.   For
  further information,  consult  Hayes,  Brown,  and  Michel  (1976)  or Gundlach
  and Hayes  (1978).
                                     382

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  EVAPORATION
  DISSOLUTION
  INTO WATER
       DISPERSAL BY
       WINDS, WAVES,
       AND CURRENTS
                                                          SUPRATIDAL
                                                          ZONE*
              EMULSIFICATION
LIGHT
FRACTIONS
        HEAVY
     FRACTIONS
                                                     ENTRAPMENT
                                                     IN AND ON
                                                     BEACH
                                                     MATERIAL
                            INTERTIDAL
                            ZONE
                                     OW f
                                    TIDE'
ENTRAPMENT
IN SEDIMENTS
                                              INTERACTION WITH
                                              SUSPENDED SEDIMENTS
 Figure 9a.   Mass  balance  components (Hann et  al_. , 1978)
                                           76,000
                                               TONS
                                 20,000 TONS   TS,^
                                 CHEMICALLY    /   >w AT
                                 DISPERSED   /6.000 /
                                           t *rs\uc  f
              74,000 TONS
              EVAPORATED
                                        25,000 TONS DISAPPEARED
                                        PERHAPS UNDER BEACH
                                                    SAND
                     80,000 TONS WENT ASHORE
                                    \  20,000-25,000
                                     \  TONS RECOVERED


                                      \

                                       \

                                       \
                            230,000
Figure  9b.   Estimated fate  of oil  from Amoco Cadiz (Source:
              local  newspapers; from Hann  et al.,  1978).
                              383

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                            VOLUME OF LOAD
                   LOADS TO
                   MOVE MOUSSE
                              750 GALLONS      188,830
                             1,800 GALLONS       78,678
             noun
 252 CU. FT.
1,884 GALLONS
75,170
                            4,000 GALLONS      35,405
                            8,000 GALLONS      17,702
Figure 10.  Equivalent truck and tank car loads necessary to remove potential
          volume of mousse from shore (Hann et al., 1978).
                               384

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cadres and  contractors  also assisted in the clean-up effort.  One of the most
spectacular  responses  came from  the farmers of  Brittany  with  their intrepid
tractors and liquid manure  or "honey" wagons.  This equipment was particularly
well suited  for  use  in the sandy-rocky coastal  areas, for pumping mousse from
wherever  it became entrapped,  such  as  in coves, pools, or  from man-made en-
trapment basins or oil booms.  Hann et al_. (1978) estimated that approximately
190,000 loads  of  about 3,000 liters each  of  oil/water  emulsion were moved by
"honey wagon" to collection points for transport by truck,  tanker, or railroad
to  tankers  at the  port  of Brest.  Tankers carried the  oil/water emulsion to
refineries.   Tragedies  continued  as the small  coastal  ship,  Henrietta Bravo,
sank in heavy seas while transporting 900 tons of oil-contaminated algae which
had been arduously removed  from the shoreline of  Brittany.

     Land activities eventually became divided into four zones,  each under the
responsibility of an engineer from Direction of Equipment,  with reinforcements
from the Army.  Student  volunteers  were under administrative direction of the
Ministry of Youth and Sports.  An effort was made to enlist volunteers who had
adequate protective  clothing,  shelter,  good personal  health,  and identifica-
tion accountability  for  assignment to  specific  cadres  under  trained foreman.
Such  details  may  seem  remote  from the  focus  of this  report, but  they are
mentioned to  indicate  the  inadequacy of existing systems to respond to spill-
ages of the magnitude  of Amoco Cadiz.  There are  serious  problems in dealing
effectively with  well-meaning volunteers;  advance  planning and  training are
essential.

     Approaches to  oil  clean-up  spanned  every  possibility.   Rapid deteriora-
tion of the ship,  combined with weather problems, precluded effective removal
of  the  cargo at  sea.   High waves  acted  as a  surge  pump,  emptying  the cargo
into  the  waters.   Inflatable  booms  were  deployed along  the   coast,  but the
incredibly  heavy  seas,  high winds and 8-meter tides overwhelmed these devices
as protective mechanisms.  However, the booms did concentrate the oil and help
in controlling it  for pumping and removal efforts.

     Some downwind  areas  anticipated the petroleum influx  and  bulldozed sand
on tourist  beaches  above  the intertidal zone.  After the clean-up, beach sand
was graded over the cleaned zone.

     Petroleum dispersants were  applied  offshore  with the restriction that
these chemicals  not be  used  in  waters  less than 50  meters  deep.   This arbi-
trary depth was probably unrealistic since 50 meters is actually very close to
shore which,  combined  with the  proximity  of  the  slick  and  onshore  winds,
aggravated  this  strategy  of  oil  spill  control  and mixed  much  petroleum into
highly productive  coastal  waters.  Thirty-five boats were  ultimately used to
spread dispersants north and east of Roscoff and  He de Brehat areas.

     Onshore oil  was pushed, scraped, sponged, collected in ditches,  collected
mixed with algae  and wrack resulting in immense disposal and storage problems.
On 6 April,  after the  change of  wind direction,  aerial  observations revealed
that the  volume  of  floating  and entrapped  petroleum in  the  environment was
overwhelming, even compared  to  the vast clean  up efforts  being expended.  It
has  been  stated  that  over $70 million  (U.S.)  was  spent by June  1978  and it
would be  at  least two years  more  before  "important"  areas were  completely
cleaned.

                                     385

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     In the  case of  village  shorelines,  as  exemplified at  Roscoff,  limited
detergents and high pressure water spraying was used to clean rocks.  Observa-
tions  on  21  July  revealed  evidence of  the  oiling  by  both  the  numerous tar
spots  and a notable  decrease  of molluscs  and marine  organisms  seen  at the
earlier (27 March) observations.   In July there was an extensive growth of the
alga Enteromorpha which is often  associated with nutrient or biostimulant pol-
lutats  in coastal marine waters.   Bathing beaches  along Roscoff  were being
scraped and  raked  and truck loads of the  algae  hauled  away to reduce the or-
ganic decomposition odors and blockage to water access  for beach visitors.

     Other  high  energy  beaches   looked  fresh with  clean  deposits  of sand.
Trenches  dug  20-60   cm  down   invariably  revealed a  deposit  layer  of brown
mousse,  still  pungent and  sticky.   These   oil   layers  will  likely  be  re-
excavated during winter tide cycles  and oil will  be redistributed by tidal and
surface currents  during winter  1979.

     The  Amoco Cadiz  oil  spill presented to modern technology, to man's soci-
ety  and  the ecosystem an  awesome  and  formidable challenge:   how  to protect
from,  or  mitigate the effects of  very  large oil spills.   Unlike  some other
spills, there were high levels  of science, technology, and organization avail-
able at this  time and place.

     Concentrated  study  and consideration of all aspects of this  event will
help prepare us for the possibility of future accidents.  It is clear that the
combinations of  circumstances  and possible impacts are nearly  infinite.  Yet,
it  is  also  clear that numerous preparations and steps can be taken to  improve
safeguards for  both prevention  and response.


                                ACKNOWLEDGMENTS

     This  summary is  compiled from  the  work of  a  number  of investigators.
Through the  generous   and patient support of Dr.  Lucien  Laubier,  Director of
the  Centre  Oceanologique  de Bretagne,  and many members of his staff including
Dr.  G.  Conan,  Dr.  L.   d'Ozouville,  and  Mr.  P.  de  Clarens,  it was  possible to
study  a delicate and  complicated  situation.  Dr.  J. Bergerard, Director of the
Station Biologique, 29211,  Roscoff,  generously assisted.  Dr. Louis Cabioch of
Station Biologique spent  considerable time with  the  observation  team, shared
data,  showed  undersea  video   tapes  and  provided much  insight and  research
knowledge  on  the  oil-sediment emulsion  and  effects on  benthic  communities.
Dr.  Miles 0.  Hayes,   Jacqueline  Michel  Hayes  and Erich  Gundlach  generously
shared their time,  valuable observations, and data derived from many hours of
study  of  coastal  ecosystem dynamics.  The  National  Oceanographic  and Atmo-
spheric   Administration's  Environmental  Research  Laboratory  Director,  Dr.
Wilmot  N.  Hess   is  thanked for  facilitating  the author's  second  visit  to
Brittany  and the  opportunity  to  participate as an observer at the Amoco Cadiz
Commission  meeting at  Brest.   I wish to  acknowledge  the   assistance  of my
patient spouse who contributed invaluable aid in  the preparation of the manu-
script.   Ms. Sharon Maier and  Douglas Middaugh read  and  made improvements to
the manuscript.
                                     386

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                                  REFERENCES

Anonymous,  1979.   Bibliography  of Amoco  Cadiz  Reports.   Union  of  Littoral
     Villages of Western Europe.  (ULVOE), Brest March 1979.

Bates, C.  C.   ed.  1978.   Conference  on Assessment of Ecological  Impacts  of
     Oil   Spills.   Proc.   AIBS   Conf.  Keystone  Col.  Am.   Inst.   Biol.   Sci.,
     Washington, D.C.   936pp.

Chasse',   C.  J.  M.  1972.   Economic,  sedimentaire,  et biologique  (production)
     de  Bretagne.   Ph.D.  Thesis Station Biologique de Roscoff,  Faculte  des
     Science de Universite de Brest.  293 pp.

Conan, .Gerard,  L.  D'Ozouville,  m.  Marchand  (ed.).   1978.  Amoco Cadiz  Prelim-
     inary  Observations of  the  Oil  Spill  Impact on  the  Marine  Environment.
     Proc.  Conf.  Amoco Cadiz,  Brest France  7  June  1978.   Publ. du  C.N.E.X.O.
     Act.  de  Colloque  No.  6  Centre  Oceanologique  de  Bretagne  29273  Brest
     CEDEX.

Cross, F.  A., W.  P.  Davis, D.  E.  Hoss, and  D.  A.  Wolfe.   1978.   Biological
     Observations.  In:  The Amoco  Cadiz Oil Spill.  W. N.  Hess  ed.   NOAA/EPA
     Spec.  Report.  Supt.  Documents,  LI.S.G.P.O.  Washington,  D.C.    20402.   p.
     197-215 + plates.

Gundlach,  Erick  R.  and Miles  0.  Hayes.  1978.   Investigations of  Beach  Pro-
     cesses.  In:  The  Amoco Cadiz  Oil  Spill.   W.  N.  Hess  ed.  NOAA/EPA  Spec.
     Report.  Supt.  Documents, U.S.G.P.O.  Washington, D.C.   20402.  p.  85-196 +
     plates.

Gundlach,  E.  R.   1979.   Oil  Spill  Impact on Temperate Shoreline  Environments,
     Based  on Study of the Urquiola (May 1976)  and Amoco Cadiz  (March  1978)
     Oil   Spills.   Ph.D.  Doctoral  Dissertation;  Dept.   Geology,  Univ.   So.
     Carolina.  238 pp.

Hann,  Roy  W. ,  Les Rice, Marie-Claire Trujillo, and Harry  N.  Young,  Jr.   1978.
     Oil   Spill  Cleanup  Activities.   In:  The  Amoco Cadiz  Oil  Spill.  W.  N.
     Hess  ed.  NOAA/EPA Spec.  Report.   Supt.  Documents, U.S.G.P.O. Washington,
     D.C.  20402.  p. 229-275 + plates.

Hess,  Wilmot  N. ,  ed.   1978.   The Amoco  Cadiz  Oil Spill:  A  Preliminary Scien-
     tific  Report.   NOAA/EPA  Special"  Report.   Supt.  Documents  U.S.   Gov't
     Printing Office, Washington, D.C.  20402.  283 pp. i-vi;  66  plates.

Hoebeke,   Lionel.   1978.   Le guide de la  France Polluee.  Fayoll,  Paris 75101,
     France; 175 pp.

Hyland,  Jeffrey  L.   1978.  Onshore  Survey  of Macrobenthos.   In:  The  Amoco
     Cadiz  Oil  Spill.   W.  H. Hess  ed.  NOAA/EPA Spec.  Report.   Supt.  Documents
     U.S.G.P.O. Wash.,  D.C. 20402:  p 216-228.

Milon, P.   1972.  La Mort sur  1'ile.   Crepin  - Le  Blond et  Cie Paris,  France,
     107 pp.
                                      387

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NOVA.   1979.   Black Tide.  P.B.S. Television Documentary Text From WGBH Educa-
     tional Foundation Boston, Mass.  19 pp.

Patten, S. M. ,  Jr.  and L. R. Patten.  1977.  Effects of petroleum exposure on
     hatching success  and incubation  behavior  of the Gulf  of  Alaska herring
     gull  group  (Larus  argentatus  x Laurs glaucenscens).  NOAA Env. Res. Labs
     OCSEAP Reports Boulder Colo.  22 pp.

Pinot, J.   P.  1976.   La  mer  et  la Peche; La  crise de la Peche en Bretagne in
     Geographic de la  Bretagne; Editor SKOL VREIZ Rennes,  France:  118-138.

Szaro, R.   C.  and P.  H. Albers.   1977.  Effects of external application of No.
     2  fuel  oil  on common  eider  eggs.   In:   Fate  and effects  of petroleum
     hydrocarbons  on   marine organisms  and  ecosystems.   D.   A.  Wolfe,  ed.
     Pergamon Press, N.Y.   164-167.
                                     388

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                                      APPENDIX
1 1 	
1 SECTEUR dt
| ST. RENAN
1
SECTEUR dt
LANNILIS
1
1
1
AT SEA | — |S
ACTIVITIES \^J FINISTERE
COAST ~]
PC. POL MAR
MARINE

, ,
STUDIES CHEMISTRY
EVALUATION OF
METHODS





SECTEUR dt
ROSCOFF
1


P.C PLOUDALMEZEAU
FINISTERE



1


PORT
ACTIVITIES






SECTEUR dt
PLOUGASNOU

FIN
cot

SECTEUR dt
L ANN ION
STERE J
1ST


P.C.ZONE RENNES
COTES-DU-NORD





LOGISTICS a
METHODS



SECTEUR dt
ST BRIEUC







CONSTRUCTION OF
ULTIMATE SOLID
WASTE STORAGE SYSTEMS
                         Approximate organization of the response effort.
OIL RELEASED
AT SEA
I1
WIND a WAVES ACT
ON THE OIL TO
FORM AN EMULSION
WITH WATER

i r

EMULSIO
WATER C(
INCREAJ
i

N IS
BY SURF;
)NTENT
>ES
NO
OIL REMAINS AT SEA ^ 	 -s. /"7s IT~"\ /""iS lf~^~\
UNTIL DISPERSED N0 /ruf^ni,^ YES /APPROACHING \ ROCKY /STRANDED IN\
BY NATURAL "* V GO ASHORE/ \ A ROCKY OR, J *"(pOOLS,
FORCES. yw^A&HUKty ^ANDYAREAX \ '

EMULSION IS SI
OUTGOING TIC

EMULSION IS /" HAS THE^\ .... X"lS
REFLOATED ^ "" /MOUSSPS SP. GRA^ "ฐ / ABOVI
•*- BY OUTGOING ^ V EXCEEDED 1 V HIGH
TIDE \^J.OE4?^X \^LfN
YES
SANDY
"HANDED BY
)E


IT ^S. _- EMULSIO
: NEXT\ TC' ^ rOMTFMl
WATER / , DECREA
f-f^y TO WEA

ON ROCKS
YES
N WATER
r
SES DUE
THERINO
	
YES /REMOVED BY\
                                                                         FUTURE TIDES,/
                                                                       REMAINS ON/IN
                                                                       BEACH UNTIL DEGRADED
                                                                       BY NATURAL PROCESSES
Possible pathways of oil spilled from Amoco Cadiz.
                                          389

-------
O>
SOLID
PICK-UP
BY
HAND


LOAD ONTO
FARM
WAGONS


TRANSFER
TO DUMP
TRUCKS


DELIVER TO
INTERIM OR FINAL
SOLID MATERIAL DISPOSAL
CUT VEGETATION
AT GROUND WITH
SHOVEL OR
MECHANICAL MEANS
     DRAIN
"^VEGETATION!
                       MOUSSE


NO
PUTIN
BUCKETS
YES


TRANSPORT BY
HAND, FARM
WAGON OR FRONT
END LOADER

                              IS
                         'MECHANICAL
                           EQUIPMENT
                         ^AVAILABLE?;
                              LOAD INTO HONEY
                              WAGONS AND/OR
                              VACUUM TRUCKS
DISCHARGE AT
INTERIM MOUSS
STORAGE
                                           NOTES-  I) ATTEMPT MADE TO DAM OFF MARSH TO CONTAIN MOUSSE BUT
                                                     SPRING TIDES BROKE THE DAM.

                                                   2) SPRINKLERS WERE USED IN SOME AREAS TO KEEP OIL OFF OF
                                                     CLEANED AREAS.
                               Unit process:  Cleaning of  He  Grande marsh.
              DELIVER
              WATER TO
            BOOST
            PRESSURE
                                                             yes
IN
TRUCK


DELIVER
WATER IN
WITH FIRE
TRUCK


FIRE OR
VACUUM TRUCK


SPRAY
COBBLES
WITH
D1SPERSANT


ALLOW
DRINKING
TIME


PICK UP
COBBLES WITH
FRONT END
LOADER


TRANSPORT AND
DISCHARGE AT
LOWER BEACH
LEVEL


COUNT ON SURF
ACTION TO
CLEAN AND
RETURN COBBLES
             Unit process: Cleaning of walls, rockfaces, and cobbles.
                                                     390

-------
PROCESS



     A
                                    MOUSSE
SEAWEED
^l\ ,„,,
TRANSPORT \N
FARM WAGON OR
DUMP TRUCK



DISCHARGE INTO
INTERIM BULK
SOLID WASTE
STORAGE
MOUSSE

TRANSPORT IN
TANK TRUCK



DISCHARGE IN
INTERIM MOUSSE
STORAGE
COLLECT MOUSSE
BY HAND
IN BUCKETS



TRANSFER BY
HAND TO 30
GAL. GARBAGE
CANS


COLLECT OIL
FROM GARBAGE
CANS WITH
VACUUM TRUCKS
COLLECT MOUSSE
WITH SKIMMER


TRANSFER TO
TANK TRUCK

•-
           Unit process: Removal of mousse from water surface to interim storage.
seawe

mousse
ed
TRANSPORT
BY DUMP
TRUCK OR
WAGON


DISCHARGE
INTO INTERIM
BULK SOLID
WASTE STORAGE
            Unit process:  Removal of mousse from rocky areas to interim storage.
                                        391

-------
PLACE MOUSSE
OR OILED
SAND IN
PLASTIC BAGS

PLACE OILED
SEAWEED OR
DETRITUS IN
PLASTIC BAGS






CARRY BY
HAMD TO
CENTRAL
POINT


LOAD BY HAND
ONTO WAGON
OR FRONT
END LOADER


DELIVER TO
INTERIM BAG
STORAGE

      Unit process: Removal of oiled sand, seaweed,  and detritus
                   to interim storage.
                                       NO MOUSSE/ SEAWEED SEPARATOR
LOAD 1 NTO
DUMP
TRUCKS


DISCHARGE INTO
INTERIM MOUSSE
STORAGE
Unit process: Removal of stranded mousse from beach to interim storage.
                               392

-------
   NO SEPARATION
                                                              DISCHARGE IN
                                                              ULTIMATE DISPOSAL
                                                              PITS BREST HARBOR
                                                              DISCHARGE IN
                                                              ULTIMATE DISPOSAL
                                                              PITS-TRB5ASTLE
Unit process: Movement of  mousse and oiled material from
              interim storage to disposal.
                           393

-------
                                   TECHNICAL REPORT DATA
                            (Please read Instructions on the reverse before completing)
1  REPORT NO.

  EPA-600/3-79-102
4. TITLE AND SUBTITLE
                                                           3 RECIPIENT'S ACCESSION NO.
 Management of  Bottom Sediments Containing Toxic  Substanc
 Proceedings  of the  Fourth U.S.-Japan Experts'  Meeting
 October 1978--Tokyo, Japan	
                                                           5 REPORT DATE
                                                                September 1979  issuing  dafr
                                                       >. PERFORMING ORGANIZATION CODE
7 AUTHOR(S)

 Spencer A.  Peterson and Karen K. Randolph,  editors
                                                           8 PERFORMING ORGANIZATION REPORT NO.
9. PERFORMING ORGANIZATION NAME AND ADDRESS
 Environmental  Research Laboratory--Corvallis,  OR
 Office of Research  and Development
 U.S. Environmental  Protection Agency
 Corvallis, Oregon 97330
                                                       10. PROGRAM ELEMENT NO.
                                                           1BA608
                                                       11. CONTRACT/GRANT NO.
12. SPONSORING AGENCY NAME AND ADDRESS
 same
                                                           13. TYPE OF REPORT AND PERIOD COVERED

                                                              in-house
                                                           14. SPONSORING AGENCY CODE
                                                              EPA/600/02
1i SUPPLEMENTARY NOTES              .
 Proceedings  of  the Second and Third U.S. -Japan  Experts  meeting on bottom sediments
 ^
-6
                    PEPA's Ecological Research  Series  as EPA-600/3-77-083  and
                    respectively:
16. ABSTRACT
 The United  States-Japan Ministerial Agreement  of May 1974 provided for  the  exchange
 of environmental  information in several areas  of mutual  concern.  This  report is the
 compilation of  papers  presented at the Fourth  U.S.-Japan Experts' Meeting on the
 Management  of Bottom Sediments Containing Toxic  Substances, one of the  10 identified
 problem areas.

 The first meeting was  held in Corvallis, Oregon  in  November 1975.  The  second meeting
 was hosted  by the Japanese Government in October 1976.   The third session was convened
 in November 1977  in Easton, Maryland and the fourth session (at which these papers
 we^e presented)  in Tokyo.
17.
                                KEY WORDS AND DOCUMENT ANALYSIS
                  DESCRIPTORS
 water reclamation
 sanitary engineering
 contaminants
 water pollution
 ocean bottom  sediments
 freshwater bottom  sediments
                                              b.IDENTIFIERS/OPEN ENDED TERMS
                                           toxic sediments
                                           mercury,  PCB  contamina-
                                             tion
                                           water pollution  control
                                           dredging
                                           dredged materials
                                                                     c. COSATI Held/Group
 06/F
 08/A,C,J,H
 13/B,J
18 DISTRIBUTION STATEMENT

 Release to Public
                                          19 SECURITY CLASS (This Report)
                                           unclassified
21. NO. OF PAGES
  400
                                              20 SECURITY CLASS (This page)
                                                unclassified
                                                                         22. PRICE
EPA Form 2220-1 (Rev. 4-77)
                                            394
                                                            irUS GOVERNMENT PRINTING OFFICE  1979—699-843/20

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