SEPA
           United States
           Environmental Protection
           Agency
           Environmental Sciences Research
           Laboratory
           Research Triangle Park NC 27711
EPA-600/4-79-009
February 1979
           Research and Development
Association Between
Meteorological
Conditions and High
Ozone and Sulfate
Concentrations
           A 1974 Episode  in the
           Eastern United States

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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 in related fields.
The nine series are:

      1.  Environmental  Health 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 ENVIRONMENTAL MONITORING series.
This series describes research conducted to develop new or improved methods
and  instrumentation for the identification and quantification of environmental
pollutants at the lowest conceivably significant concentrations.  It also includes
studies to determine the ambient concentrations of pollutants in the environment
and/or the variance of pollutants as a function of time or meteorological factors.
This document is available to the public through the National Technical Informa-
tion Service, Springfield, Virginia 22161.

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                                              EPA-600/4-79-009
                                              February 1979
ASSOCIATION BETWEEN METEOROLOGICAL CONDITIONS
  AND HIGH OZONE AND SULFATE CONCENTRATIONS
 A 1974 Episode in the Eastern United States
                      by
              Gerard A. DeMarrais
      Meteorology and Assessment Division
  Environmental  Sciences Research Laboratory
      Research Triangle Park, N.C.  27711
  ENVIRONMENTAL SCIENCES RESEARCH LABORATORY
      OFFICE OF RESEARCH AND DEVELOPMENT
     U.S. ENVIRONMENTAL PROTECTION AGENCY
     RESEARCH TRIANGLE PARK, N.C.  27711

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                                 DISCLAIMER


     This report has been reviewed by the Office of Research  and  Development,
U.S. Environmental Protection Agency, and approved for publication.   Mention
of trade names or commerical products does not constitute endorsement or
recommendation for use.
     Mr. DeMarrais is a meteorologist in the Meteorology and Assessment
Division, Environmental Sciences Research Laboratory, Environmental  Research
Center, Research Triangle Park, N.C. 27711.  He is on assignment from the
National Oceanic and Atmospheric Administration, U.S. Department of Commerce.
                                     ii

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                                   ABSTRACT
                   2
     A 1,000,000 km  area of the Eastern United States had sulfate concentra-
tions exceeding 10 yg/m  on July 10, 1974, and there were indications that
parts of the area had high concentrations on prior days.   The meteorology
associated with the high concentrations and correlations  of high ozone and
sulfate concentrations are discussed.   It appeared that slow moving and
subsiding air contributed to the high concentrations of both pollutants.   Long
range transport, as shown by trajectory analyses,  was a factor in the problems
in most areas, but the worst situations with regards to sulfates were asso-
ciated with emissions from nearby,  upwind sources.  While high ozone concen-
trations were observed immediately prior to high sulfate concentrations in
many areas, there were high sulfate concentrations that were not associated
with high ozone concentrations.   In the latter situation, the high sulfate
concentrations were associated with air which had  earlier movement over areas
with high S02 emission.
                                      m

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                                   CONTENTS

Abstract	      iii

Figures	       vi

Tables	     y-j^-

Postscript and Acknowledgement	       ix

     1.  Introduction 	        1

     2.  Conclusions	        2

     3.  Background and Methods 	        4
              Sulfates, reactions producing sulfates, and measuring of
              sulfates	        4
              The ozone episode 	        5
              The SO,, to sul fate conversion and long-range transport.
              Diurnal variations of sul fates	        7
              Meteorological conditions associated with high concentra-
              tions of ozone and sulfates 	        7
              Potential source areas of ozone and sulfate precursors.        y
              Meteorological resources	        9

     4.  Results	       11
              Background	       11
              Sulfate data	       11
              The ozone data	       14
              Temperature data	       15
              Visibility	       16
              Synoptic weather situation	       18
              Other meteorological observations 	       20
              Trajectories of the surface-to-1000-m layer 	       20

     5.  Summary	       25

References	    27-30

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                                  FIGURES
Number                                                                Page
  1.  Annual  hydrocarbon emissions by state in  1973  (1000 tons).  .  .  .  ;31
  2.  Annual  S09 emissions from power plants by state  in  1974
      (1000 tons).
  3.  Locations of sulfate monitoring stations  of state  and  local
      agencies (see Table 1 for station names)	
  4.  Sulfate concentrations (yg/m )  July 10,  1974 	
32
33
34
  5.  Station locations (see Table 4 for station names)  TVA network.  .
                                                                        i
  6.  Maximum hourly ozone concentrations (ppb)  July 6,  1974 	   j3^
  7.  Maximum hourly ozone concentration (ppb)  July 7,  1974	|3?
                                                                        i
  8.  Maximum hourly ozone concentration (ppb)  July 8,  1974	,38
                                                                        j
  9.  Maximum hourly ozone concentration (ppb)  July 9,  1974. 	   i3^
                                                                        i
                                                                        ! ._
 10.  Maximum hourly ozone concentrations (ppb)  July 10, 1974.  ....
 11.  Maximum hourly ozone concentration (ppb) July 11, 1974
 41
 42
 12.  Maximum temperatures (°F) July 6, 1974 	
 13.  Maximum temperatures (°F) July 7, 1974	i43
 14.  Maximum temperatures (°F) July 8, 1974	i44
 15.  Maximum temperatures (°F) July 9, 1974	i45
 16.  Maximum temperatures (°F) July 10, 1974. .  .	'46
 17.  Visibility  (miles) July 6, 1974, 1 p.m., e.s.t	4?
 18.  Visibility  (miles) July 7, 1974, 1 p.m., e.s.t	48
 19.  Visibility  (miles) July 8, 1974, 1 p.m., e.s.t	•  4$
 20.  Visibility  (miles) July 9, 1974, 1 p.m., e.s.t.  .	  50
                                      vi

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                              FIGURES   (Contined)

Number                                                                 Page

 21.  Visibility (miles)  July  10,  1974,  1  p.m., e.s.t	   51

 22.  Daily weather maps, July 6,  1974	   52

 23.  Rainfall during sulfate  sampling  period of July 10, 1974  • • •  •   53

 24.  48-h trajectories  (12-h  segments)  of layers of air between the
      surface and 1000 m  for selected cities, July 6, 19/4  (arrival
      time 1 p.m., e.s.t.)	   54

 25.  47-h trajectories  (12-h  segments)  of layers of air between the
      surface and 1000 m  for selected cities, July 7, 1974  (arrival
      time 1 p.m., e.s.t.)	   55

 26.  48-h trajectories  (12-h  segments)  of layers of air between the
      surface and 1000 m  for selected cities, July 8, 1974  (arrival
      time 1 p.m., e.s.t.)	   56

 27.  48-h trajectories  (12-h  segments)  of layers of air between the
      surface and 1000 m  for selected cities, July 9, 1974  (arrival
      time 1 p.m., e.s.t.)	   57

 28.  48-h trajectories  (12-h  segments)  of layers of air between the
      surface and 1000 m  for selected cities, July 10,  1974 (arrival
      time 1 p.m. e.s.t.).	   58
                                     vii

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                                   TABLES

Number                                                                 Page

  1.  Names  of Stations  in Sulfate  Monitoring Network (see Figure 3)
      for station locations)  	   59

  2.  Sulfate Concentrations  (yg/m3) at CHESS Stations in the New York
      City Area, July 6-11, 1974	   60

  3.  Sulfate Concentrations  (yg/m  ) at Electric Power Industry Sites    |
      in Northern United States, July  6-11,  1974  	   |61

  4.  Station Names, TVA Network (see  Figure 5  for station locations).   j62

  5.  Sulfate Concentrations  (yg/m3) TVA Network, July 3-11, 1974.  .  .63-64
                                     viii

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                                POSTSCRIPT
     After the final draft of this report was completed,  a technical
article examining the same sulfate episode was published.   This article,
Spatial and Temporal Distributions of Airborne Sulfate in Parts of the
United States in Atmospheric Environment, V.12, 735-752,  (1978), by
G. Hidy et al., briefly discusses with isoplethed maps the high sulfate
concentrations of July 8-11, 1974.
     This EPA report differs from the technical article in that major
emphasis is given to the coexistence of high ozone and high sulfate
concentrations.   In addition, more consideration is given to details.
These details show that isoplething masks out discrepancies and on
occasion does not show a significant feature; for example, the isoplethed
                                                                  3
map for July 10 indicates a concentration of approximately 10 yg/m  in
the vicinity of West Virginia whereas two stations in the area showed
concentrations four and five times as great.
                               ACKNOWLEDGEMENT
     The patience of Mrs. Hazel Hevenor in retyping the many  drafts of
this report was appreciated.
                                     IX

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                                SECTION 1
                              INTRODUCTION
     Sulfate concentrations are frequently above average when ozone
                                  1                                         2
concentrations are relatively high .   In a southern California investigation ,
it was shown that an 8-d sulfate episode coincided with an ozone episode.
To further test the cofrequency hypothesis, a period was sought during
which high ozone concentrations occurred in that 16-state area* that has
                                                                            3
consistently shown higher sulfate concentrations than the rest of the nation .
Such an ozone event occurred over the area during July 6-10, 1974, and a
preliminary correlation of the ozone concentrations and meteorological
conditions was previously noted .  In this report the available sulfate
data (they are not as abundant as ozone data), ozone concentrations, and
meteorological conditions for the period are discussed.
* This 16-state area is east of the Mississippi River, and is roughly bounded
  by Illinois and Massachusetts to the north and Tennessee and North Carolina
  to the south.
                                      1

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                                 SECTION  2
                                CONCLUSIONS
     On the basis of the analysis of the  daily ozone, sulfate, and meteorologi-
cal data, the following conclusions are drawn:
     1.  A large-scale ozone episode occurred over the  Northeastern United
     States from July 6 to 10, 1974, and  midway  through the  episode sulfate
                                                                        2
     concentrations became high and eventually spread over a 1,000,000 km  area
     of the Eastern United States.
     2.  The ozone episode was initially  associated with only the air behind
     a cold front that pushed southeastward  over the area on July 6.  The
     air mass eventually became the warmest  of the year (most locations  in
     the ozone episode area had the highest  temperatures of  the  year during
     this 5-d period) and was characterized  by slow movement at  the surface
     and aloft (stagnation) and subsidence.  The high sulfate concentrations
     each day were not restricted to the  high temperature areas  but were
     associated with the slow moving and  subsiding air.
     3.  The areas of high ozone concentrations  on each day  did  not correspond
     to the areas with restricted visibility or  precipitation.   The areas of
     high sulfate concentrations on each  day corresponded somewhat to the
     areas with restricted visibility during several days when  the sulfate data
     were  limited  and  on  the  one day  (July  10)  with abundant sulfate data.   The
     area  with high  sulfate concentrations  on July 10  corresponded to the
     area  with rainfall.   After  the passage of a front  toward the end of
     the period, the ozone concentrations were reduced,  and  the restrictions
     to visibility eliminated,  but the sulfate concentrations remained  high.

     4.  The  trajectory analysis frequently showed that air  with a high
     ozone or sulfate  concentration at a receptor had  had a  high concentration

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at an earlier time in an upwind location;  long-range  transport, although
limited by stagnation, did occur.   However,  at  times  air arrived from
areas that did not show a high ozone  or sulfate concentration, but at
these times the air usually came from an area that was  a large emitter
of precursors.

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                                  SECTION 3
                           BACKGROUND AND METHODS
SULFATES, REACTIONS PRODUCING SULFATES,  AND MEASURING OF SULFATES
     Most sulfur in the atmosphere, land surface,  and water exists as the
hexavalent oxidized sulfate ion (SO^pJ in such diverse forms as sulfuric
acid; amonium bisulfates; calcium sulfate (the major component of gypsum);
magnesium sulfate (epsom salts); sodium and potassium sulfates (in seawater);
and other metal salts, such as copper, nickel, iron, lead,  and zinc sulfates  .
     On a global scale, natural sources contribute about two-thirds of the
sulfur compounds in the atmosphere by weight,  and  human activities the re-
mainder.  In the continental United States, probably 90% of the atmospheric
sulfur is the result of anthropogenic emissions in the form of sulfur dioxide
(S02) .  Most of the S02 is oxidized to the sulfate form within a few days,
and, while this oxidation is taking place, the pollutants in the air can be
transported long distances; the sulfate receptors  may be hundreds of km from
the sources of primary emissions .
     The important mechanisms by which S09 is converted to sulfuric acid and
             36
sulfate salts  '  are:  1) direct photopxidation; 2) indirect photooxidation;
3) air oxidation in liquid droplets; 4) catalyzed  oxidation in liquid drop-
lets; and 5) catalyzed oxidation on dry surfaces.
     A substantial fraction of  the man-made sulfate problem is believed to
be associated with S02 emitted  by large power olants  . The 16-state area
with the higher sulfate concentrations correlates spatially with  high S02
emission density, high rainfall acidity patterns,  and a high density of
power plant locations  .
     The majority of  sulfate data evaluated in this report were  supplied by
the National Aerometric Data Bank  (NADB) and  the CHESS  (Community Health and
Environmental  Surveillance  System) program of the U.S.  Environmental  Protection

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Agency (EPA).  The sulfate data in the NADB came from State and local  air
pollution control agencies and were generally collected every 12th day in
accord with a preset schedule (in July 1974 nearly all stations had data for
the 10th and 22nd);  some stations sampled on additional days at random
times.  The stations in the CHESS program were operated every day.  Sulfate
data from stations in a network operated by the electric power industry  and
49 stations in a Tennessee Valley Authority (TVA) network are also considered
in the analyses.  Each sulfate measurement is made from a small strip  of
filter on which suspended particulate had been collected in a high volume
air sampler.  Each sampling period is 24-h, and the filters are changed at
midnight (local standard time).  The filter strip is extracted with water,
and a portion of the aqueous extract is analyzed for sulfate by the methyl
thymol blue method.
     At the present  time no National Ambient Air Quality Standard (NAAQS)
exists for sulfates. In an EPA position paper  on the regulation of atmos-
pheric sulfates the  highest concentration tentatively associated with  adverse
health effects was reported to be 10 yg/m  (24-h average) and in this  report
                                   3
concentrations greater than 10 yg/m  are labeled high.
THE OZONE EPISODE
     The investigation of the ozone episode  examined data from approximately
100 stations in the  Eastern United States extending from Ohio and Massachusetts
                                                                         4
in the north to Tennessee and North Carolina in the south.  In the report
data for 50 representative stations in 11 states are presented (no ozone
data were available  for West Virginia and South Carolina).  Ozone monitoring
stations are usually operated by State and local agencies, with the State
agency being responsible for providing the Federal Government with a near-
complete and accurate record.  More than two dozen agencies collected the
analyzed data.  One  station in Richmond, Virginia, used an ultraviolet
Dasibi instrument, but all others employed a chemiluminescence instrument.
     The current NAAQS (hourly value) for ozone*, not  to be exceeded more
than once a year, is 160  g/m3 or 80 ppb8; in this report, when the NAAQS is
violated, a concentration is called high.  The ozone data presented came
from the NADB.
*It has been proposed that the NAAQS be revised upward to 200 yg/nT
                                     5

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THE S02 TO SULFATE CONVERSION AND LONG-RANGE TRANSPORT
     The conversion of S02 to sulfate in the air and the possibility of
long-range transport of the sulfate have been reported extensively    ;
there are many observations and findings but the agreement is not universal.
                          Q
One group of investigators  found no clear evidence of long-range transport,
another investigator   reported obvious transport out to 1000 km, and others11
found transport readily occurred but was limited to several  hundred km.  An
incomplete knowledge of the meteorology, chemistry, and timing of processes
in the conversion of man-made S02 to sulfates and of the eventual return to
the surface by uptake and precipitation is the cause of the disagreement
about the long-range transport of sulfates.  Various investigators have
                                                      12
hypothesized about features of the processes.  Georgii  , basing his hypothesis
on observations over Central Europe, noted three important features.  First,
the vertical S02 concentration decreases rapidly with altitude, reaching
half the ground concentration at 800 to 1200 m above the surface.  Second,
seasonal variations of the S02 concentration are limited to the 2000 m
immediately above the surface.  Third, inversions prevent, and convection
accelerates the transport of S02 into higher layers; above the inversion and
haze layers, the S02 concentration decreased markedly, whereas the sulfate
concentration is not much influenced by the thermal structure of the atmos-
phere.  The difference between the gas phase and liquid phase conversion of
S02 to sulfate was noted by Kellogg et al.   .  They reported the gas phase
conversion showed a half-life for S02 of  12 d while, when S02 was dissolved
in fog or cloud droplets, particularly where metal salts were present  to
                                                                    14
serve as catalysts, the S02 rapidly (within  hours) oxidized.  Weber
estimated that 50% of the S02 emitted by  power plants and the space heating
chimneys in the Frankfurt area was oxidized  in the first 20 min  to  1 hr of
                                                                       15
travel time during the winter (in relatively moist air).  Atkins et al.
in discussing sulfate concentrations over Britain, stated that the  concentra-
tions were indicative of the history of the  air mass  several  days earlier and
showed air in which oxidation of S00 occurred at distances up to  1000  km  up-
                                      IE
wind over Central Europe.  The authors    further stated  that  the  sulfate  was
removed from the atmosphere almost  solely by rainfall.

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     Nisbet   stated that after transport  and  oxidation, sulfur is returned
to earth by four principal  routes:
     1.  absorption of gaseous  SCL  by  the  soil  or  vegetation;
     2.  deposition of SOp in  rain  or  snow;
     3.  deposition of sulfates in  rain  or snow; and
     4.  dry deposition of particles containing sulfates.
DIURNAL VARIATIONS OF SULFATES
     Since many meteorological  phenomena (e.g., wind  speeds, temperature,
relative humidity) usually show marked diurnal  variations,  a knowledge of the
diurnal variations of sulfates could indicate  which meteorological phenomena
might account for sulfate variations.  Unfortunately, investigators  of the
diurnal variations of sulfate  concentrations have  produced  inconsistent  and
conflicting results15'17"20.

METEOROLOGICAL CONDITIONS ASSOCIATED WITH  HIGH CONCENTRATIONS  OF  OZONE AND
SULFATES
     Considerable documentation of the meteorology associated  with high
                                                         24
oxidant concentrations has accumulated*.  Middleton et al.   ,  in  1950
reported that high ozone concentrations  occurred with weak  winds  and stagnant
air.  Other early, comprehensive investigations of the Los  Angeles ozone
              22-24
concentrations      related variations in  concentrations  to variations in the
following:  intensity and duration of  solar  radiation; surface temperature;
the depth of  the  polluted layer (the top coincided with the base of the
                                                                           Of"
subsidence  inversion); and wind speed and direction.    Following the report
that winds  aloft  in the  Los Angeles area are important in transporting that
which  the author  describes as  "second-hand ozone" to unsuspecting downwind
areas,  investigators examined  the three dimensional  air movements and
transport in  the  200-km  long Basin.  Evidence26"28 confirms that high ozone
concentrations are frequently  in the air aloft, even within the subsidence
layer,  and  that these ozone-laden layers move with the winds aloft.
Eventually, some  of the  ozone  is brought to the surface in daytime mixing.
In recent years the long-range transport of ozone has been reported in many
                   oq TO
areas  of the  nation

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      As previously noted, direct and indirect photochemical  processes are
 important in the production of sulfates, so intense solar radiation and
 abundant sunshine are conducive to high concentrations.   Whenever there is
 good vertical motion in the daytime and ozone is carried aloft, SO^ in the
 presence of this ozone aloft is oxidized at appreciable rates at night as
                       34
 well as in the daytime  .  The heterogeneous rate of oxidation of S09 to
                                          qc qc                      ^ qc
 sulfate is dependent on relative humidity  '  .   In a laboratory study  , no
 oxidation  was detected when the relative humidity was less than 70%, while
 at  higher humidities the oxidation rates were considerable (possibly because
 catalyst particles changed from solid form into solution drop form).  Low
                                                                 37
 speeds tend to keep sulfates near the sulfur sources; Bushtuveva   found
 that concentrations of sulfuric acid aerosol during "calm days" were 4.5
 times greater than during days with winds averaging over 5 m/s.  Sulfate
                                            1o qo                       qg
 concentrations will also vary with rainfall  '  .   Early investigators
 found that the sulfate concentration of rainwater decreased with an increased
 rate of rainfall; they suggested that there was a limited quantity of
 sulfate in the lower atmosphere, which  is removed in each period of pre-
                                Ifl
 cipitation.  In the other study   it was reported that the sulfate concentra-
 declined sharply  as a result of rainfall and increased rapidly after the
 rainfall ended.  Sulfate concentrations in urban areas tend to peak in the
 third quarter of the year  (July, August, September) but occasionally peak
                      39
 in  the second quarter   .

POTENTIAL  SOURCE  AREAS OF OZONE AND  SULFATE  PRECURSORS
     Since  ozone  and sulfates are  seldom emitted  directly  to  the atmosphere,
their presence is  dependent  on the emission  of precursors—pollutants  that
after being emitted  into the atmosphere react and become  ozone  and  sulfates.
Hydrocarbon emissions  are considered  important forerunners  of ozone, and S02
is  the primary precursor of sulfates.   Because differences  in the  observed
spatial  patterns  of  concentrations of ozone  and sulfates  could  be  due
to  differences in  the  emission patterns of the precursors,  data on  the emission
patterns were  sought.

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     Figure 1  shows  the annual  emissions  of  hydrocarbons  in tons  for 1973  (the
most recent year available) for each  state in  the  study area.   The  large ton-
nages in Illinois,  New York, Ohio,  Michigan, and Pennsylvania  show  that those
states are major sources of ozone precursors.  When  emission density (emissions
per km ) is considered, a number of smaller  states also have to be  designated as
large emitters—Massachusetts,  Connecticut,  New Jersey, and Maryland.  Thus,
the large emitters  are primarily in the  northern part  of  the Eastern United
States.
     Figure 2  shows  the annual  SCL emissions from  power plants for  1974.   The
states with large emissions were_Michigan,  Illinois, Indiana,  Ohio, Pennsylvania,
New York, West Virginia, Kentucky, Tennessee and Alabama.  The states  of
Massachusetts, Connecticut,  Rhode  Island, New Jersey, Delaware, Maryland
                                                                2
and Virginia and the District of Columbia on an emissions per  km   basis
have  to be considered  small  emitters.

METEOROLOGICAL RESOURCES
      Daily weather data contained  in the Local Climatological   Data   for 86
National Weather Service (NWS) stations in the Eastern United  States were
evaluated.  Major emphasis was given to maximum temperatures,   visibilities,
and the occurrences of precipitation at these  stations.   Daily Weather
    41
Maps   were reviewed;  this publication has maps for the United States  showing
the conditions that prevailed at the surface and at 500 mb, about  5500 m
above the surface, at  7 a.m., Eastern Standard Time each day.   These maps
were  used to locate fronts,  centers of high and low pressure,   and  areas of
precipitation and to relate  the wind speeds and directions to   high concentra-
tions.

     Trajectory analyses   were used  to  supplement the data from the Daily
Weather Maps by showing the likely paths of the layer of air prior to  arrival
in the area.  The trajectory analyses are based on the wind data from  the
rawinsonde observations scheduled at  7 a.m.  and 7  p.m. and the winds aloft
observations at 1 a.m. and 1 p.m. each day.   In the basic calculation, a
point along the trajectory is determined every 3  h and data within a radius
of 300 nautical miles  (556 km)  are evaluated.   The model  includes a

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distance weighting factor (the closest observations  receive the greatest
weight), an alignment weighting factor (observations  upwind and downwind
receive the greatest weight), and a height  weighting  factor  (the thicker
the subpart of the trajectory layer that  the  wind  represents, the  greater the
weight).  Trajectory segments are linked  together  to  produce a complete tra-
jectory for the desired period of time.  Trajectories are  usually  started from
a source or receptor four times daily, 1  and  7  a.m.  and  1  and 7 p.m.   In this
report, trajectories are used to show the backward movement of the surface-
to 1000 m layer in 12-h segments for a number of designated cities.  These
trajectories are approximations and thus  become progressively less reliable
with each added segment.  In this report  the  trajectories  are limited  to
48 h.  A point on a trajectory indicates  the  general  area  and not  a
specific location where a layer of air was  located at an earlier time.
                                       10

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                                SECTION 4
                                 RESULTS
BACKGROUND
     Whereas the air quality data collection  program  throughout  the nation
provides continuous  hourly  data for ozone  concentrations, sulfate date are
gathered only every  12th day and for a  24-h period.   During early July 1974
the sulfate monitoring network, operated by the  State and local  agencies,
collected samples on the 10th.   Since this was only 1 d during the ozone
episode, an ozone-sulfate correlation could be misleading unless the sulfate
concentrations were  shown to be representative of  the period.  Accordingly,
the basic sulfate data were supplemented by:  1) Norfolk data in the NADB
for July 8 and 9; 2) data from  a four-station network operated daily by the
CHESS program in the New York City area; 3) data from nine stations in a
network  operated daily by  the  electric power industry in the Northeastern
United States; and 4) data  from 49 monitoring stations at 18 locations in a
TVA network (this network collected samples on every  sixth day).
     The number of State and local sulfate monitoring stations in the Eastern
United States that operated on  July 10  was 83.   Although much more numerous in
the north, there were enough stations in the  south to delineate  the area
with high concentrations.  The  ozone stations were so numerous in the North-
east that all could  not be  conveniently plotted  on a  map, so a number are
not on the ozone figures that follow.  In  contrast to the Northeast, there
was no ozone data for West  Virginia, South Carolina,  Georgia, and Alabama
and a very limited amount of data for Michigan and Indiana.
SULFATE DATA
     The locations of the State and local  sulfate  monitoring stations are
shown in Figure 3, and the  names of the stations are  shown in Table 1.  The
sulfate data for the 83 stations on July 10 are  shown in Figure  4.  High
                                     11

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concentrations prevailed in an area from Boston  to Atlanta  to Chicago  to  Boston,
                       2                                         3
an area of 1,000,000 km .   The concentrations  ranged from 63 yg/m   in
southern Pennsylvania to 4 in northern  Indiana with approximately three-fourths
                                                       3
of the stations showing concentrations  exceeding 10 yg/m  .  Not to  be  over-
looked are the numerous areas reporting extremes in concentrations  within short
distances, for example:  1) southern Michigan, 42 (Lansing) vs 9  (Flint); 2)
northern Indiana 25 (East  Chicago)vs 4  (South  Bend); 3) southeastern Pennsyl-
vania, 63 (York) vs 7  (Lancaster); and  4) northeastern New  Jersey,  29  (Eliza-
beth) vs 7 (Newark).  These contrasts indicate that individual observations
are representative of limited areas and that judgments about regional  con-
ditions should be based on observations from several locations.   With  more
                                  p
than 60 stations in the million km  area showing concentrations in  excess of.
       3
10 ug/rn , it is concluded that an episode of at  least a 1-d duration existed
in the region.
     The data for Norfolk showed that the sulfate concentrations  for July 8,  9,
                                                 o
and 10 were respectively 5.0, 12.7, and 14.7 yg/m .  These  limited  data
indicate that Norfolk's relatively high concentrations extended back to  the
9th, but not to the 8th.
     The data for the four CHESS stations in the New York City area for  July  6
to 11 are shown in Table 2.  In the New York City area the  sulfate  concentra-
tions were markedly higher on the 10th than on the 5 other  days.  The  con*
centrations were relatively low on the 8th, increased on  the  9th, then
increased two or three fold on the 10th.
     The data for the nine electric power company stations  which gave
coverage from Illinois to New York, are shown  in Table  3.  The overall indi-
cation is that most of the area had concentrations in excess  of  10  yg/m   most
of the time.  Three Indiana stations (and the  fourth  for  2  d)  had high values
on all 6 d and the values were comparable to those at the NADB  stations  on
July 10 (see Figure 4).  The only places and times at which low  values were
recorded were Huntington on the 6th and 7th, Scranton on  all  days but  the
                                                      22
9th, and Albany on the 6th, 7th, and llth.  Tong et al    evaluating the
concentrations at each of  these stations, showed the following monthly average
concentrations  (yg/m3) for July 1974;  about 22  at the four Indiana stations
                                      12

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and at Huntington,  27 at Wheeling,  16  at Collins,  13 at Scranton, and 9 at
Albany.  Concentration levels  twice the  average values occurred at only one
of the four stations in Indiana  and then on  the llth, on the 8th and 9th at
Huntington, on the  7th, 8th, and 9th at  Wheeling,  and on the 9th at Scranton
and Albany.

     The 18 locations from which the TVA obtained sulfate  data are  shown  in
Figure 5,  and Table 4 lists the names of the locations.  The 6-d  sampling
schedule provided large amounts of data for July 3 and  9 and a few  data  points
for July 6, 7, and 8.  The observed concentrations on  these days  and  the
average concentration observed during the July sampling days are  shown  in
Table  5.   The data for the 3rd indicate that the area  had  many locations
                 3
exceeding  10  g/m , but the limited data for the 6th,  7th, and 8th  indicate
                                                                    3
that concentrations were relatively low; most were less than 10  g/m  ,  and all
showed concentrations that were about half or less than the July  average.
                                                                       3
On July 9, a majority of locations had concentrations  exceeding 10   g/m  (again
most stations had concentrations below the July average).   In a number  of
areas  there were sharp contrasts in concentrations within  short distances;
for example, in northeast Alabama between Widows Creek  (13) and Hytop (15),
in northwest Alabama between Colbert (3) and Muscle Shoals (9), and in
western Kentucky between Paradise  (10) and Land Between  the Lakes (16).
     The indication of the TVA data is that the concentrations on July  9 over
the Southeastern United States were similar to those in the State and local
network on July 10 (Figure 4), but on the 2 prior days  they were  lower.
     The composite picture drawn from the sulfate data  from the four
                             2
sources is: 1) a 1,000,000 km  area in the eastern United  States  had  high
sulfate concentrations on July 10; 2) whereas some places  had concentrations
exceeding  10  g/m  on earlier days, the period of markedly high concentra-
tions  over an extensive area appeared to be July 8 to  10;  3) there  was
an apparent movement from west to east of a peak concentration with the
peak passing through West Virginia on the 8th and 9th,  Pennsylvania and New
York on the 9th, and the New York City-Long Island area (and possibly Norfolk)
on the 10th; and 4) although no peak moved through the  southern part of the
affected area, the area of high concentrations appeared to spread southward

                                    •13

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from July 8 to 9.
THE OZONE DATA
     The extent of the high concentrations  of ozone  on  each  day  from
July 6 through 11 is shown in Figures 6 to  11.  On July 5  only a half-dozen
locations had NAAQS violations while on July 6 (Figure  6)  slightly  more
than one-third of the stations had violations.  The  high concentrations,  on
this date, were restricted to the northern  areas and extended from  Chicago to
eastern Connecticut in three separate areas.  On July 7 (Figure  7), a  Sunday,
almost two-thirds of the stations recorded  violations of the standard, and the
higher concentrations were observed farther south than  they  had  been on  the
6th.  There were only two separate areas of high concentrations  (the area of
low concentration on July 6 in central  New  York and  Pennsylvania was eliminated);
they were separated by an area of low concentrations oriented  north-south
through western Ohio and eastern Kentucky and Tennessee.  On July 8 (Figure  8)
about three-fourths of the locations had NAAQS violations, and again the
two separate areas with high concentrations were seen.   This was the day
that the majority of stations recorded their highest concentrations.   July  9
(Figure 9) was the day with the greatest number of locations showing
violations as more than three-fourths had concentrations exceeding  80  ppb.
There were still indications of eastern and western  areas  with high concentra-
tions, but the problem was moderating in the latter. On July  10 (Figure 10)
less than half of the stations had violations, since the high  concentrations
-were concentrated in the Richmond-to-New York corridor and Pennsylvania
and Ohio.  On July 11  (Figure 11) only five locations had  violations,
while 57 did not show  violations; the regional ozone episode had ended
by July  11.
     The overall picture is that a large area in the Northeastern United States
had high ozone concentrations from July 6  to  10.  The concentrations and
the number of stations with high concentrations were greatest on July 8  and 9.
There Was no gradual spreading of the area with high concentrations nor  an
apparent movement of a peak concentration  across the area, as there had  been
with the sulfate concentrations.
                                      14

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TEMPERATURE DATA
     The initial high ozone concentrations occurred on July 6,  so the analysis
of the temperature data start with that  day.   Figure 12, shows  the maximum
temperatures reported at 86 NWS stations in the  Eastern United  States.  In
order to locate the relatively warm areas, each  station that observed a maximum
temperature 2.7°C (5°F) or more warmer than its  July average is marked in
bolder print.  Only three small warm areas are shown on July 6, indicating
that high temperatures were not associated with  the initial occurrence of
high ozone concentrations.  The overall  comparison of July 6 maximum tempera-
tures and the July average indicated that this was a relatively cool day over
the whole area.
     On July 7 (Figure 13) a large area  across the northern section of the
Eastern United States and two separate stations  had relatively-high tem-
peratures.  Many stations with high ozone concentrations  (Figure 7) were
within the area that observed high temperatures, but a large number were
south of the area.  Although a few of the Electric Power  Industry stations
showed high sul-fate concentrations in the high temperature area, most
stations in the area (Tables 2 and 3) had low  concentrations.
     On July 8 (Figure 14) the area with high  temperatures included all of
the northernmost stations, and the southern boundary was  farther south than  it
was on July 7.  It is interesting that temperatures in the north were on the
average about 2.7°C (5°F) warmer than those in the south.  The  areas with high
ozone concentrations (Figure 8) were for the most part in the same area as those
with high temperatures; the stations with high ozone concentrations extended
a little farther south.  Comparison of the  limited sulfate data with the
temperature pattern showed no consistent agreement; monitoring  stations
(Tables 2 and 3) within the area of high temperatures  showed  a  wide variation
in concentrations.
     On July 9 (Figure 15) the area with relatively high  temperatures covered
the greatest area that it was to cover during  this period, and  17  stations had
the highest temperature of the month on  this date.  The area  with  high ozone
concentrations (Figure 9) was approximately the  same as that  with  high
temperatures.  Although many stations in the high temperature area  had high
                                     15

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sulfate concentrations, some stations  outside  the area had high sulfate con-
centrations (Tables 3 and 5).

     On July 10 (Figure 16) two large  separate areas and a station in West
Virginia had high temperatures.  The high-temperature eastern area had many
locations with high ozone concentrations,  but  many locations with high
concentrations were not in the areas with  high temperatures.  The area with
high sulfate concentrations on this  day (Figure  4) was practically the
entire area; the areas of high sulfate and relatively high temperature were
not similar.
     Overall, the indication is that the initial high ozone concentrations
occurred before the high temperatures, but through the worst of the ozone
episode the area of high ozone concentrations  was almost the same as the
area with high temperatures.  However, in  the  case of the sulfates there "did"
not appear to be a good spatial agreement  with regard to the areas of high
temperature and high sulfates.  Even if one were to consider a lag between
the high temperatures and high sulfates, and compare the area of high
temperatures of July 9 with the area of high sulfates of July 10, there did
not appear to be agreement.
VISIBILITY
     The NWS records always note the visibility  restriction  (fog, haze, smoke;,
precipitation, etc) whenever the visibility is less than 11.25 km  (7 mi).  The
visibility observations that are presented are for 1 p.m. Eastern Standard
Time, a time in the day when relative  humidities are usually low and fog  is
reported infrequently. " In the figures to follow the visibilities and obstruc-
tions to visibility are shown for the  86 NWS stations  in the east, and  areas
with obstructions to visibility, other than rain, are  delineated.   In the text
that follows, poor and restricted visibility are used  interchangeably.
     On July 6  (Figure 17) the first day with  high ozone concentrations,  the
restricted visibility area was a 350-km wide band, running  from  just  below
New York City to near Richmond and extending 1300 km to  southern  Indiana  in
the west.  Outside the restricted visibility area, 16  km (10 mi) or  greater
visibility was  recorded at most stations.  The majority  of  stations  with  high
ozone concentrations  (Figure 6) were to the north of the restricted  visibility

                                      16

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area, and the majority of the ozone monitoring  stations  in  the poor visibility
area did not have NAAQS violations.  With  regard  to  the  limited sulfate
data (Tables 2,3, and 5), most of the stations with low concentrations were
outside the restricted visibility area, and  most  with high  concentrations were
inside the area.
     On July 7 (Figure 18) the restricted  visibility area extended from
southern Michigan to northern Kentucky, then eastward to the  Washington,
D. C., area.  Most of the ozone stations (Figure  7)  in the  poor visibility
areas did not have violations of the NAAQS.   To the  northeast of the
restricted visibility area, the ozone concentrations were high, and visibilities
generally 16 km (10 mi) or more: to the west of the  poor visibility area, all
but one NWS station had a visibility of 12.9 km (8 mi) or more, while all five
ozone monitoring stations showed violations. The EPRI sulfate monitoring sta-
tions (Table 3) with high concentrations were generally  in  the restricted
visibility area, while the relatively clean  EPRI  stations  (Scranton, Albany),
CHESS stations (Table 2), and TVA stations (Table 5) were outside the area.
     On July 8 (Figure 19) the area of poor  visibility covered the Midwest
and extended into northern Virginia, Georgia, and southwestern Tennessee.
Although many of the ozone monitoring stations  (Figure 9) in  the poor
visibility area did have NAAQS violations, a much greater proportion
of stations had violations in the relatively good visibility  area along the
east coast.  The sulfate data for Norfolk, and  from  the  EPRI  (Table 3) and
CHESS (Table 2) networks, although limited,  indicate that the stations with
high concentrations were generally in the  area  with  restricted visibility and
those with low concentrations outside the  area.   The one TVA  station reporting
on this day, Loves Mill in southwest Virginia (Table 5), had  a low concentra-
tion and was in an area with good visibility.
     On July 9 (Figure 20) most of the Northeastern  United  States had poor
visibility, and a large majority of the ozone monitoring stations (Figure 9)
in the area had NAAQS violations.  The sulfate  data  from Norfolk, and from the
EPRI (Table 3) and CHESS stations (Table 2), indicate that  stations with Con-
                                's
centrations in excess of 10 yg/m  were generally  in  the  restricted visibility
area, but the TVA data (Table 5) indicate  that  a  large area with high concen-
trations did not have restricted visibility.
                                     17

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     On July 10 (Figure 21) the area of restricted  visibility was  smaller
than it was on July 9, but still covered a large portion  of  the  Eastern
United States.  Most stations with high ozone concentrations (Figure  10)
were in the restricted visibility area.  The sulfate data for July 10 were
abundant (Figure 4) and show that the area of high  sulfate concentrations
was larger than the area with obstructions to visibility.

      Overall, the  indication is that  the  area of restricted visibility was
 not similar to the area with high  ozone concentrations,  except during the
 height of  the ozone alert, July 9  and possibly  July  10.   On the days with
 limited sulfate data, the areas of restricted visibility and high sulfate
 concentrations were similar, but on the day with the most abundant sulfate
 data, the  area with high  concentrations was ;a little larger than  the,	
 restricted vj'sfb 11 ity area.
 SYNOPTIC WEATHER SITUATION
      The broad scale weather conditions or synoptic  weather data  of  July 6
 to 10 are  documented in the Daily  Weather Maps   .  The conditions on the
 first day, Jjuly 6, are shown in Figure 22; maps for  the  period  July  7 to 10
 were also  examined, but were omitted because there were  only small or gradual
 changes after July 6.
      the main features ofrthe swrface weather map^were:   1) a stationary
 front extending from below New England, west southwestward  to northwest
 Tennessee;  2) a high pressure area centered over Lake Erie; and 3) the western
 extensioh  of the Bermuda high pressure area over the Southeastern United
 States.. The location of the front practically  coincided with the southern
 boundary of the area of high ozone concentrations  (Figure 6); the high
 ozone concentrations were restricted to the air mass north  of the front.  The
 area of reduced visibility (Figure 17) included locations on both sides  of
 the front  and was  practically centered on the front.  The sulfate data  from
 the CHESS  stations (Table 2) showed that  the air immediately north of  the
 front was  relatively clean, whereas the EPRI data  (Table 3) showed that most
 stations north of  the front had high concentrations.
                                      18

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    "On July 7 there was just a  remnant  of the  stationary front  immediately
south of Pennsylvania and a weak high  over the  east was  the  only feature on
the surface maps on July 8 and 9.   The July 10  map showed a  cold front was
over southern Michigan,  New York,  and  New England.  Throughout the  period
the areas with high ozone concentrations (Figures 7-10)  and  poor visibility
(Figures 18-21) expanded as the  two high pressure areas  of July  6 amalgamated.
High sulfate concentrations also gradually spread over the entire area as the
weak high pressure dominated the weather.  Behind the  cold front of July 10
the ozone concentrations were reduced  and the visibility improved,  but the
sulfate concentrations (Figure 4)  appeared to be unaffected.
     The 500-mb map for  July 6 (Figure 22b) was typical  of July  6 to 10.
High pressure with subsiding air over  the Eastern United States  was the
dominant feature of the  maps for the period.  The strong flow out of the
extreme Southeastern United States feeding the flow over the northern tier
of states in the east was a feature of the maps from July 6  to 8.  Warm air
was being transported into the high over the east by this flow.
     Overall, the synoptic situation was one that showed stagnation at the
surface and aloft and subsiding  air over a large part  of the Eastern United
States.  This stagnation coupled with  the subsidence appeared to have marked
effect on the observed ozone and sulfate concentrations  and  visibility.  The
high ozone concentrations were restricted to one air mass in which  the number
of stations with high concentrations increased with time as  the  air moved slowly
and became progressively wanner  due to an influx of air  from warmer areas and
the subsidence.  In addition, the high ozone concentrations  were not restricted
to the western side of the surface high  pressure area, as reported  by Lyons  and
Cole  , but were observed throughout the high pressure area.  The sulfate
concentrations when the  data were limited were highest near  the  center of
the surface high pressure area,  but on the one day with  abundant data, high
concentrations were widespread and extended beyond the area  of poor visibility
at the surface.  The visibilities were restricted  in  the vicinity of the
slow-moving front early  in the period, and then the obstructions spread
throughout the slow-moving air mass.  Next, the obstructions were
eliminated as the rapidly moving front passed through  the area toward the
end of the period.  The  passage  of the front was associated  with an improvement

                                     19

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in visibility and with a reduction in the ozone  concentrations,  but did not
simultaneously reduce the high sulfate concentrations.
OTHER. METEOROLOGICAL OBSERVTIUNS
     Meteorological parameters other than those  previously  summarized were
also examined.  These included minimum temperatures,  visibility  at 7 a.m.,
relative humidity at 6 a.m. and noon, percent of possible sunshine, and
precipitation for 24-h periods.  The minimum temperatures,  like  the
maximum temperatures, were relatively high.   None of  the other parameters
showed a pattern that was considered noteworthy  except  precipitation.
During the period of July 6 to 9, the rainfall was usually  in the form of
afternoon or evening showers and these occurred  over  widely separated areas.
The rainfall on these 4 d did not appear to  be associated with the
ozone concentrations; some areas with high concentrations had rainfall
while most had no precipitation.  The spatial distribution  of sulfate
monitoring stations during these 4 d was inadequate for making comparisons
with rainfall patterns.
     On July 10 (Figure 23) the rainfall was extensive. The rainfall again
occurred,-over both areas with high ozone and low ozone  concentrations.   With
regard to sulfate concentrations (Figure 4)  the  area  with high sulfate
concentrations was about the same as the area that recorded rainfall.  There
appeared to be no correlation between the 24-h rainfall and restricted visi-
bility (at 1 p.m.) patterns, although there  was  a rather consistent  relation-
ship for 5 d (July 6-10); the southern part  of the area with poor visibility
generally had rainfall, while the areas to the north  and west did not.
TRAJECTORIES OF THE SURFACE-TO-1000-m LAYER
     Backward trajectories indicate the general  area from which  air  has  come
to designated locations.  The trajectories may be used in  conjunction with
air quality data to show that air came from an area that already had a
pollution burden.  The upper limit of the layer for which trajectories  are
determined is the conservative height of 1000 m; the bulk of the pollution
in the atmosphere would be contained in the layer between the surface and
1000 m.  Trajectories on occasion show that air from one area may be moved
in a period of 48 h to more than one downwind location.  During periods
of weak winds, July 6-10,  1974, for example,  trajectories readily crossed one
                                    •  20

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another, and on some occasions air arrived  in  various areas  by circuitous
routes.
     Backward trajectories for 48-h periods for  selected  stations, mostly
state capitals, for July 6 to 10,  1974,  are shown  in Figures  24  to 28.
Although four trajectories were determined  for each day,  only that for the
ending time of 1 p.m. is shown. This  ending time  is close to the time when
maximum hourly ozone concentrations generally  occur, and  the trajectories for
this ending time were considered representative  of the  four  daily trajectories.
The station coverage is dense in order to show the various areas from which
air moved into almost every state  and  the fact that air from over one area
reached widely separated receptors.
     Figure 24 shows the trajectories  for July 6.  These  trajectories indicate
that the high ozone concentrations (Figure  6)  in the northeast were  associated
with rapid flows from the west and northwest,  while the high concentrations
in the northwest were associated with  circuitous trajectories.   The  limited
sulfate data (Tables 2,3, and 5)  showed that  the  lower concentrations
occurred in areas that had long and direct  trajectories,  while  the high
concentrations occurred in the area where the  air  traveled a circuitous
path.  The area of poor visibility (Figure  17) occurred in the  boundary
area between the flows with the component from the north  (in the northern
third of the area) and the flows with  the component from  the south.   Comparison
of individual trajectories also showed interesting results.   The trajectories
ending in central Connecticut (which had high  ozone concentrations)  and
eastern Massachusetts (which had low ozone  concentrations)  traversed locations
that were generally much closer than the terminal  points  (about 150  km
apart; although  the  air came  to the two locations from the  same general  source
areas these downwind receptors observed different concentrations.  The flows
ending in southeast  New York  and south-central Pennsylvania  (both areas had
high ozone concentrations) traversed common areas in eastern Ohio and western
Pennsylvania.  A point that was common to  three plotted  trajectories, those
ending in central and northeast Illinois and central  Indiana, was 150 km
south of Chicago  (not shown is a trajectory for central  Ohio which also
crossed the area).   The cities at the end  of these trajectories had high
ozone concentrations.
     On July 7  (Figure 25) the trajectories were markedly shorter than those
                                     21

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for July 6 indicating that the air movement  on July 7 was  considerably
less than that on July 5.   Most of the flow  into the southern stations was
from the south, and the area did not have  high ozone (Figure 7) or sulfate
(Table 5) concentrations.   The flows into  the northern stations were from
the west and northwest, and the stations in  this area were those  that had
high ozone and sulfate (Table 3) concentrations and restricted visibility
(Figure 18).  The areas with high ozone concentrations in  the north were
downwind of areas that had air with an ozone burden on July 6 (Figure 6).
The unpolluted areas in the south had flows  from relatively clean areas.
If the ozone burden in the air was no more than 2  d old, the high contra-
trations at the individual stations must have been caused  by emissions
within a state or from a state immediately adjacent to it; most of the
trajectories originated in one state and terminated in an  adjacent state.
The sulfate data in Table 3 show that Wheeling had a markedly high concen-
tration, and the trajectory ending in West Virginia indicated that that  area
had the least air movement; the high sulfate concentration was associated with
emissions from areas very close to Wheeling;
     On July 8 (Figure 26) in all areas except the extreme northeast,
the trajectories were short.  In the west  and southeast  the movement
was from the south, and in the northeast  it  was from the northwest.   High
ozone concentrations were observed in practically  all  areas (Figure 8).
Most of the southerly flows brought air from areas that  had relatively
low concentrations oh July 6 and 7 and normally emitted  a  small  amount
of ozone precursors (Figure 1) yet the downwind stations observed high
ozone concentrations.  The high ozone concentrations were  not always  associated
with flows from areas having high ozone concentrations on  earlier days.
The limited sulfate data in Tables 2, 3,  and 5  indicate  that  the  area with  the
highest sulfate concentrations, West Virginia,  had the trajectory with  the
shortest travel distance; the observed high  concentrations at Huntington and
Wheeling were associated with emissions from nearby sources.
     On July 9 (Figure 27) the trajectories  were  about as  long  or slightly
longer than those on July 8.  In the northeast  the flows were mostly  from
the west, the ozone concentrations were high (Figure  9), and  on prior days
the air was over areas with high ozone concentrations  (Figures  8 and  9).

                                     22

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In the northwest and south, where ozone concentrations  were declining
(Figure 10 vs Figure 9), the flow during the most recent 12 h was
from the west or southwest, while earlier it was  from the south; the upwind
areas had relatively low concentrations on July 8.   It  is interesting  that
the area of high ozone concentrations is associated more with flows from the
areas of large emissions of ozone precursors (Figure 1) than the area  with
the shortest trajectories (i.e.,  the weakest winds). The limited  sulfate
data (Tables 2,3, and 5) showed  high sulfate concentrations at Wheeling,
Huntington, and the one Lawrenceburg (near Cincinnati)  station.  The move-
ment of air over West Virginia was so slow that the polluted air could not
have come from a great distance;  at the Lawrenceburg site for the  most
recent 12-h flow, the flow was along the Ohio River Valley.
      On July 10 (Figure 28) the  lengths of the trajectories were  generally
longer than they had been on July 9.  The trajectories  show that areas
with high ozone concentrations (Figure 10) were downwind of areas  that also
had high concentrations on the prior days and are normally expected to have  large
emissions of ozone precursors. The NADB sulfate data (Figure 4) show  that
high concentrations occurred throughout the area.  The  most recent of  the
12-h trajectory segments show that many of the high concentrations in  the
north and east were associated with a flow out of the northwest.   Earlier, how-
ever, all trajectories were generally of shorter length and showed movements
over all areas normally associated with large emissions of SOp  (Figure 2);
the high concentrations were likely more affected by earlier slow  movement
over source areas than by the most recent 12-h flow.
      Overall, the trajectory analyses showed that the  high concentrations
of ozone were associated with flows across the northern tier of states--
the area where the sources of ozone precursors are most numerous.  The
indication was that air having an ozone violation on one day frequently
had shown a violation on an earlier day at an upwind location.  Although
the trajectories indicated that interstate transport of ozone occurred,
48-h movements were frequently restricted to flows between adjacent
states; long-range transport was  limited due to the stagnation  conditions.
The highest sulfate concentrations were generally associated with  the  shortest
                                     23

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trajectories; local emissions appeared to be the major cause  of  the worst
sulfate conditions.  On the day when the sulfates were an area-wide problem,
practically all of the high concentrations could be traced back  to slow  move-
ment over source areas.
                                      24

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                                 SECTION  5
                                  SUMMARY
                             2
1.  On July 10 a 1,000,000 km  area  of the  Eastern  United  States observed
    high sulfate concentrations.   The  concentrations  appeared  to be  high over
    a large area from July 8 to 10,  and the peak  in concentration  appeared
    to move eastward during the period.  On July  6  and  7 a few stations in
    the north had high concentrations.
2.  The ozone episode covered the Northeastern  United States from  July 6 to
    10.  Although the concentrations and  number of  stations with high concen-
    trations was greatest on July 8  and 9,  the  ozone  problem was fairly
    widespread and severe on all  5 d.   There was  no apparent movement of
    a peak concentration across the  area.
3.  The maximum temperature data analysis showed  that:  a) there were high con-
    centrations of ozone over a large  area  before there were high  surface
    temperatures; b) during the worst  of  the ozone  episode, the area with
    high ozone concentrations was almost  the same as  the area  with high
    temperatures; and c) during the  worst of the  sulfate episode,  the area
    with high concentrations covered a much larger  area than that  with high
    temperatures.

4.  The visibility data analyses showed that:  a) the area with high ozone
    concentrations did not correspond  day by day  to the area with  restricted
    visibility; and b) there did appear to  be considerable similarity  in
    areas with poor visibility and high sulfate concentrations on  those days
    when the data were limited, and  to a  lesser degree  on  the  day  when the
    sulfate data were abundant.  Areas with low sulfate concentrations  were
    generally outside the areas with restricted visibility.
5.  The synoptic weather analysis showed  that:  a)  large-scale stagnation oc-
    curred at the surface and aloft; b) the high  ozone  concentrations were not
                                     25

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     restricted to the western side of the air  mass  but  spread  throughout it;
     d) the sulfate concentrations were initially  high near  the center  of the
     surface high pressure area (based on a limited  amount of sulfate data),
     but eventually the whole area had high sulfate  concentrations;  e)  the
     restrictions to visibility were initially  associated with  a  front
     (obstructions were present on both sides)  but after July 6 the  high
     sulfate concentrations generally occurred  in  the areas  of  restricted
     visibility and low sulfate concentrations  occurred  outside the  poor
     visibility areas; and f) a frontal passage toward the end  of the period
     was associated with a lowering of the ozone concentrations and  the
     elimination of restrictions to visibility  but did hot affect sulfate
     cohcehtratidn.-
6.    the rainfall analyses showed that:  a) there  was no.correlation between
     rainfall arid ozone concentrations; and b)  the area  of rainfall  oh  July 10
     had boundaries corresponding to the area with high  sulfate concentrations.
7.    the trajectory analysis showed that:  a) high dzori£ concentrations were
     usually associated with" flows over th£ area of  highest  emissions of ozone
     bre'cursors and air that had ah ozone burden before"  it arrived in the
     area Where the high concentration  was detected;  b) long-range transport
     was involved in moving the dzo'he-laderi layers;  but  the  transport  was
     limited by the stagnation conditions prevailing;  c) the highest sulfate
     concentrations were associated with the shortest  trajectories;  and d) on
     the day with the area-wide p'foblem with su'ifates,  the  high concentra-
     tions Were traced back to slow-moving air  over the  area with high
     precursor emissions.
                                    26

-------
                                   REFERENCES

 1.  Greeley, R. S., R. P. Ouellette, J.  T.  Stone,  and  S.  Wilcox.   Sulfates
     and the Environment - A Review.   The MITRE Corporation,  McLean,  Virginia,
     1975.  131 pp.

 2.  DeMarrais, G. A.  Meteorological Conditions During a  Sulfate  Episode  in
     Southern California.  EPA-600/4-78-022, U.S.  Environmental  Protection
     Agency, Research Triangle Park,  North Carolina,  1978, 1978.   32  pp.

 3.  Strategies and Air Standards Division.   Position Paper on  Regulation  of
     Atmospheric Sulfates.  EPA-450/2-75-007, U.S.  Environmental  Protection
     Agency, Research Triangle Park,  North Carolina,  1975. 87  pp.

 4.  DeMarrais, G. A.  The 1974 Ozone Episode in the  Baltimore-to-Richmond
     Corridor.  EPA-600/4-87-016, U.S. Environmental  Protection  Agency,
     Research Triangle Park, North Carolina, 1978.   33  pp.

 5.  Altshuller, A. P.   Atmospheric  Sulfur  Dioxide and Sulfate.   Environ.
     Sci. Techno!., 7(8):709-712, 1973.

 |6.  Wilson, W. E.~, R. J. Charlsbn, R. B. Husar, K. T.  Whitby,  and D. Blumenthal
 :    Sulfates in the Atmosphere.  EPA-600/7-77-021.  U. S. Environmental  Pro-
     tection Agency, Research Triangle Park, North Carolina,  1977.  29 pp.

 7.  Environmental Research and Technology,  Inc.  Design of the  Sulfate
     Regional Experiment (SURE) EC-125.   Volume III Appendices.   Report prepared
     for the Electric Power Institute, Palo  Alto,  California, 1976.

 8.  National Air Pollution Control Administration.   Air Quality Criteria  for
     Photochemical Oxidants.  AP-63.   U.S. Department of Health,  Education,
     and Welfare, Washington, D.C., 1970.  178 pp.

 9.  Lipfert, F. W., H. Cowherd, and  S.  Kaufman.  The Temporal  and Spatial
     Variations of Atmospheric Suspended  Sulfates  in  the Northeastern United
     States.  Paper 77-39.2 presented at  Air Pollution  Control  Association
     Annual Meeting, Toronto, Ontario, June  20-24,  1977.

10.  Rhode, H.  A Study of the Sulfur Budget for the  Atmosphere  over  Northern
     Europe.  Tell us XXIV:128-137, 1972.

11.  Summers, P. W., and B.  Hitchon.   Source and Budget of Sulfate in Precipita-
     tion for Central Alberta, Canada,  J. Air Poll.  Control  Assoc. 23:194-199,
     1973.
                                       27

-------
12.  Georgii, H. W.  Contribution  to  the Atmospheric Sulfur Budget.  J.
     Geophys. Res. 75:2365-2371,  1970.

13.  Kellogg, W. W., R.  D.  Cadle,  E.  R. Allen, A. L. Lazrus, and E. A. Martell.
     The Sulfur Cycle.  Science 175:587-596, 1972.

14.  Weber, E.  Contribution to the Residence Time of Sulfur Dioxide in a
     Polluted Atmosphere.   J.  Geophys. Res. 75:2909-2914, 1970.

15.  Atkins, D.H.F., R.  A.  Cox, and A.E.J.  Eggleton.  Photochemical Ozone
     and Sulphuric Acid  Aerosol Formation in the Atmosphere over Southern
     England.  Nature 235:372-376, 1972.

16.  Nisbet, I.  Sulfates  and Acidity in Precipitation:  Their Relationship to
     Emissions and Regional  Transport of Sulfur Oxides.  Chapter 7 in Air
     Quality and Stationary Source Emission Control.  Committee on Public Works
     United States Senate,  Washington, D.C., 1975.  pp. 276-312.

17.  Meszaros, E.  Seasonal  and Diurnal Variations of the Size Distribution of
     Atmospheric Sulfate Particles.  Tell us XXII, 2:235-238, 1970.

18.  Wagman, J., R. E. Lee, Jr.,  and  C. J.  Axt.   Influence of Some Atmospheric
     Variables on the Concentration and Particle  Size Distribution of Sulfate in
     Urban Air.  Atmos.  Environ.  1:479-489, 1967.

19.  Tohg, E. Y., G. M.  Hidy, T.  F. Lavery, and F. Berlandi.  Regional and Local
     Aspects of Atmospheric Sulfates  in the Northeast Quadrant of the United
     States.  In Preprint Volume:   Third Symposium on Atmospheric Turbulence,
     Diffusion, and Air Quality, Amer. Meteorol.  Soc., Raleigh, North Carolina,
     1976.  pp. 307-310.

20.  Corn, M., and L. Demaio.  Particulate  Sulfates in Pittsburgh Air.   J. Air
     Poll. Control Assoc.  15:26-30, 1965.

21.  Middleton, J. T., J.  B. Kendrick, and  H. W.  Schwalm.   Injury  to  Herbaceous
     Plants by Smog or Air Pollution.  Plant Disease Reporter, 34(9):245-252,
     1950.

22.  Ne1burger, M. and J.  Edinger. Meteorology of the Los Angeles Basin.
     Report No. 1^ Southern California Air  Pollution Foundation, Los  Angeles,
     California, 1954.  97 pp.

23.  Renzettij N. A., Editor.  An Aerometric Survey of the  Los Angeles Basin,
     August-November 1954.  Report No. 9, Air  Pollution  Foundation, Los  Angeles,
     California, 1955.  334 pp.

24.  Hitchcock, L. B., W.  L. Faith, M. Nieburger, N. A.  Renzetti,  and L.  H.
     Rogers.  Air Pollution Situation in  Los Angeles-An  Aerometric Survey.
     In:   Proceedings of the Third National Air  Pollution  Symposium,  Pasadena,
     California, 1955.  pp 12-23.
                                      28

-------
25.  Lea, D. A.  Vertical  Ozone Distribution  in the Lower Troposphere Near an
     Urban Pollution Complex.  J.  Appl.  Meteorol., 7:252-267, 1968.

26.  Gloria, H. R., G. Bradburn, R.  F. Reinisch,  J. N.  Pitts, Jr., J. V. Behar,
     and L. Zafonte.  Airborne Survey of Major Air Basins in California.  J.
     Air. Poll. Control Assoc., 24(7) :645-652, 1974.

27.  Blumenthal, D. L., L. A. Farrow, and T.  A. Weber.  The Effects of Variations
     in Bulk Meteorological Parameters on Ozone Concentrations.   In Preprint
     Volume:  Symposium on Atmospheric Diffusion  and Air Pollution, Amer.
     Meteorol. Soc., Santa Barbara,  California, 1974.   pp. 115-120.

28.  Kauper, E. K., and B. L. Niemann.   Los Angeles to  Ventura over Water Ozone
     Transport Study.  Report prepared for California Air Resources Board by
     Metro Monitoring Services, Covina,  California, 1975.  54 pp.

29.  Tommerdahl, J. B.,  C. E. Decker, L. A.  Ripperton, and J.J.B. Worth.
     Airborne Ozone Monitoring Program.   Part 3 of Investigation  of Ozone
     and Ozone Precursor Concentrations  at Nonurban Locations in  Eastern United
     States.  Report prepared for Environmental  Protection Agency by Research
     Triangle Institute, Research Triangle Park,  North  Carolina,  Contract
     GB-02-1343, 1974.  44 pp.

30.  Lovelace, D. E., T. Kapsalis, R. C. Bourke,  and P. P. Cook.   Indianapolis
     1974 Summer Ozone Study.  Report of Indianapolis Center for  Advanced
     Research, Inc., Indianapolis, Indiana, 1975.  118  pp.

31.  Department of Natural Resources. Ozone  Monitoring-Wisconsin, Summer 1974.
     State of Wisconsin, madison, Wisconsin,  1975.  23  pp.

32.  Martinez, E. L.  Temporal-Spatial Variations of Nonurban Ozone Concentra-
     tions and Related Meteorological Factors.   Presented at Conference on Air
     Quality Measurements sponsored by Southwest  Section of the Air Pollution
     Control Association, Austin, Texas, 1975.   27 pp.

33.  Karl, T. R., and G. A. DeMarrais.   Meteorological  Conditions Conducive to
     High Levels of Ozone.  In:  Report  of International Conference on  Photo-
     chemical Oxidant Pollution and Its  Control  (preprint), September 12-17,
     1976, Research Triangle Park, North Carolina, 1977.  pp 75-88.

34.  Cox, R. A.,  and S. A. Penkett.  Photo-Oxidantion  of S02  in  the Atmosphere.
     J. Chem. Soc., Faraday Soc., 68:1735, 1972.

35.  Penkett, S. A.  Oxidation of S0? and Other  Atmospheric Gases by Ozone in
     Aqueous Solution.  Nature (Physical Science), 240:105-106, 1972.

36.  Cheng,  R. T.,  J.  0.  Frohliger^ and  M. Corn.  Aerosol  Stabilization for
     Laboratory Studies of Aerosol-Gas  Interactions.   J.   Air Poll.  Control
     Assoc., 21:138-142,  1971.
                                    29

-------
37.  Bushtuveva, K. A.   Ratio of Sulfur Dioxide  and Sulfuric Acid Aerosol in
     Atmospheric Air, in Relation to  Meteorological Conditions.  Gigiena i
     Sanitariyce, 11:11-13, 1954.

38.  Larson, T. E., and I.  Hettick.   Mineral  Composition of Rainwater.
     Tellus 8:191-197,  1956.

39.  Frank, N. H., and  N.  C.  Possiel, Jr.   Seasonality  and Regional Trends in
     Atmospheric Sulfates.   Paper presented to American Chemical Society, San
     Francisco, California, August 30-September  3, 1976.

40.  Environmental Data Service.  Local Climatological  Data.  Monthly Summaries
     for R. E. Byrd International Airport  (Richmond), Washington National Air-
     port, and Friendship International Airport  (Baltimore).  National Oceanic
     and Atmospheric Administration,  Asheville,  North Carolina, July 1973.

41.  Environmental Data Service (NOAA). Daily Weather  Maps (for selected
     weeks).  U.S. Government Printing Office, Washington, D.C., 1974.

42.  Heffter, J. L., A. D.  Taylor, and G.  J.  Ferber.    A Regional-Continental
     Scale Transport, Diffusion and Deposition Model.   National Oceanic  and
     Atmospheric Administration Tech. Memo ERL-ARL-50.  Air Resources
     Laboratories, Silver Spring, Maryland, 1975.  28 pp.

43.  Lyons, W. A. and H. S. Cole.  Photochemical Oxidant Transport:  Mesoscale
     Lake Breeze and Synoptic-Scale Aspects.   J. Appl.  Meteorol.,  15:733-743,
     1976.
                                       30

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Figure 1.  Annual hydrocarbon emissions by state in 1973 (1000 tons).

-------
Figure 2.  Annual S02 emissions from power plants by state in 1974 (1000 tons).




                                       32

-------
Figure 3. Locations of sulfate monitoring stations of state and local agencies (see Table
1  for station names).

                                          33

-------
                                   BOLD NUMBERS SHOW
                                    CONCENTRATIONS > 10ug/m3
Figure 4.  Sulfate concentrations (/Kj/m3) July 10, 1974.
                        34

-------
OJ
en
                                                                                                           30e
                                                                                     (NUMBERS ENCIRCLED
                                                                                     INDICATE RURAL SITE)
                                                                                     	\   X
                             Figure 5. Station locations (see Table 4 for station names) TVA network.

-------
                                             BOLD NUMBERS SHOW
                                             NAAQS VIOLATION
                                             (M = MISSING)
                                                    \
                                                                    40"
                                                                    35°
Figure 6.  Maximum hourly ozone concentrations (ppb) Jujy 6, 1974.
                                36

-------
                                        BOLD NUMBERS SHOW NAAQS
                                         VIOLATIONS (M = MISSING)
                                             N  \
                                                                  40°
                                                                  35°
Figure 7.  Maximum hourly ozone concentration (ppb) July 7, 1974.
                              37

-------
                                            BOLD NUMBERS SHOW
                                             NAAQS VIOLATION
                                             (M = MISSING)

                                               ,-A
Figure 8.  Maximum hourly ozone concentration (ppb) July 8, 1974.
                                 38

-------
                                            BOLD NUMBERS SHOW
                                             NAAQS VIOLATION
                                             (M = MISSING)
Figure 9.  Maximum hourly ozone concentration (ppb) July 9, 1974.
                                 39

-------
Figure 10.. Maximum hourly ozone concentrations (ppb) July 10, 1974.
                              40

-------
                                               BOLD NUMBERS SHOW
                                                NAAQS VIOLATIONS
                                                (M = MISSING)
Figure 11.  Maximum hourly ozone concentration (ppb) July 11,  1974.
                              41

-------
                      BOLD NUMBERS SHOW TEMPERATURES
                       5° OR MORE ABOVE STATION AVERAGE
                       FOR JULY 1974
Figure 12.  Maximum temperatures (  F) July 6, 1974.
                       42

-------
                          BOLD NUMBERS SHOW TEMPERATURES
                           5° OR MORE ABOVE STATION
                           AVERAGE FOR JULY 1974
                                    :\
                                                           40°
                                                           35°
                                                           30"
Figure 13.  Maximum temperatures (°F) July 1, 1974.
                        43

-------
                           BOLD NUMBERS SHOW TEMPERATURES
                            50 OR MORE ABOVE STATION
                            AVERAGE FOR JULY 1974
                              \          i	\\
                                                           40°
                                                            35°
                                                            30°
Figure 14.  Maximum temperatures (°F) July 8, 1974.
                        44

-------
                          BOLD NUMBERS SHOW TEMPERATURES
                          5° OR MORE ABOVE STATION
                          AVERAGE FOR JULY 1974
Figure 15.  Maximum temperatures (°F) July 9, 1974.
                        45

-------
                        BOLD NUMBERS SHOW TEMPERATURES 5°
                        OR MORE ABOVE STATION AVERAGE
                        FOR JULY 1974
Figure 16.  Maximum temperatures (°F) July 10, 1974.
                      46

-------
                                                          40°
                                                          35"
                                                          30"
                                           OBSTRUCTIONS

                                             F = FOG
                                             H = HAZE
                                             K = SMOKE
                                             R = RAIN
Figure 17. Visibility (miles) July 6, 1974, 1300 EST.
                          4/

-------
                                               = FOG
                                              H = HAZE
                                              K = SMOKE
                                              R = RAIN
Fjgurp 18. Visibility (mjles) July 7, 1974, 1300 ESJ.
                          48

-------
                                              F = FOG
                                               = HAZE
                                              K=SMOKE
                                              R= RAIN
                                                           40°
                                                           35°
                                                           30"
Figure 19. Visibility (miles) July 8, 1974, 1300 EST.
                          49

-------
                                            = FOG
                                           H = HAZE
                                           K=SMOKE
                                           R= RAIN
Figure 20. Visibility (miles) July 9, 1974, 1300 EST.
                      50

-------
                                                             40°
                                                             35°
                                               OBSTRUCTIONS

                                                  = FOG
                                                H=HAZE
                                                K=SMOKE
                                                R=RAIN
                                                             30°
Figure 21. Visibility (miles) July 10, 1974, 1300 EST.
                           51

-------

                  (a)  Surface weather map
C.00-MU L 'RAH HEIGHT CONTOURS _
U  / 00 4 M  E.S.T
                        (b)  500-mb map
                              i


        Figure 22.  Daily weather maps for July 6,  1974
52

-------
                               AMOUNTS IN HUNDRETHS OF INCHES
                                       T = TRACE
                                                                25°
Figure 23. Rainfall during sulfate sampling period of July 10, 1974.
                            53

-------
Figure 24. 48-h trajectories (12-h segments) of layers of air between the
surface and 1000 m for selected cities, July 6, 1974 (arrival time 1 p.m.,
e.s.t.).
                                   54

-------
                                                                      30°
                                                                      25°
Figure 25.48-h trajectories (12-h segments) of layers of air between the
surface and  1000 m for selected cities, July 7, 1974 (arrival time 1 p.m.,
e.s.t.).
                                     55

-------
                                                                     25°
Figure 26. 48,-h trajectories (12-h segments) of layers of air between the
surface and 1000 m for selected cities, July 8, 1974 (arrival time 1 p.m.,
e.s.t.).
                                   56

-------
                                                                       25°
Figure  27. 48-h trajectories (12-h segments) of layers of air between the
  surface and 1000 m for selected cities, July 9, 1974 (arrival time T p.m.,
  e.s.t.).
                                       57

-------
                                                                      25°
Figure 28. 48-h trajectories (12-h segments) of .layers of air between the
surface and 1000 m for selected cities, July 10, 1974 (arrival time 1 p.m.,
e.s.t.}.
                                     58

-------
               TABLE 1.  NAMES OF STATIONS IN SULFATE MONITORING
                  NETWORK (see Figure 3 for station  locations)
 1.  Ashland, KY
 2.  Bowling Green, KY
.3.  Covington, KY
 4.  Charleston, WV
 5.  South Charleston, WV
 6.  Hampton, VA
 7.  Norfolk, VA
 8.  Portsmouth, VA
 9.  Lynchburg, VA
10.  Richmond, VA
11.  Roanoke, VA
12.  Wythe Cnty, VA
13.  Chattanooga, TN
14.  Knoxville, TN
15.  Memphis, TN
16.  Nashville, TN
17.  East St. Louis, 1L
18.  Moline, IL
19.  Peoria, IL
20.  Rock Island, IL
21.  Springfield, IL.
22.  Atlanta, GA
23.  Columbus, GA
24.  Columbia, SC
25.  Union Cnty., SC
26.  Richland Cnty., SC
27.  Charlotte, NC
28.  Durham, NC
29.  Greensboro, NC
30.  East Chicago, IN
31.  Evansville, IN
32.  Gary, IN
33.  Indianapolis, IN
34.  Terre Haute, IN
35.  Monroe Cnty., IN
36.  Parke Cnty., IN
37.  South Bend, IN
38.  Solomons Island, MD
39.  Akron, OH
40.  Canton, OH
41.  Cincinnati, OH
42.  Allentown, PA
43.  Bethlehem, PA
44.  Clarion, PA
45.  Erie, PA
46.  Hazel ton, PA
47.  Lancaster, PA
48.  Pittsburgh, PA
49.  Scranton, PA
50.  Warminster, PA
51.  Wilkes Barre, PA
52.  York, PA
53.  Albany, NY
54.  New York City, NY
55.  Niagara Falls. NY
56.  Rochester, NY
57;  Syracuse, NY
58.  Utica, NY
59.  Yonkers, NY
60.  Hartford, CT
61.  New Haven, CT
62.  Waterbury, CT
63.  Elizabeth, NJ
64.  Glassboro, NJ
65.  Newark, NJ
 66.   Perth Amboy, NJ
 67.  Trenton, NJ
 68.   Providence, RI
 69.  Washington Cnty., RI
 70.  Cambridge, MA
 71.   Fall River, MA
 72.  Springfield, MA
 73.  Worcester, MA
 74.   Burlington, VT
 75.  Orange Cnty., VT
 76.  Smyrna,  DE
 77.   Newark,  DE
 78.   Dearborn, MI
 79.   Detroit, MI
i80.   Flint, MI
 81.   Lansing, MI
 82.   Saginaw, MI
 83.  Trenton, MI
                                      59

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           TABLE 2.   SULFATE  CONCENTRATIONS (yg/m3) AT CHESS STATIONS
                        IN  THE  NEW  YORK CITY AREA, JULY 6-11, 1974

"^\Date
STATION ^^^X^
Rlverhead
Queens
Brooklyn
Bronx
July
6
4.9
6.8
M .
9.3
July
7
7.1
12.6
M
10.6
July
8
6.2
7.9
12.2
6.0
July
9
1 2 .5
15,6
16.2
M
July
10
27.2
38.5
54.1
M
July
11
11.0
11;2
M
M

M * Missing
                                      60

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           TABLE 3.  SULFATE CONCENTRATIONS (yg/m3) AT ELECTRIC POWER
           INDUSTRY SITES IN NORTHERN.UNITED STATES, JULY 6-11, 1974

^v. Date
Station ^s.
Collins, JL
Rockport, ID
Madison, ID
Lawrenburg I, ID
Lawrenburg II, ID
Huntington, M
Wheeling, W
Scranton, PA
Albany, NY
July
6
M
15.9
18.5
31.6
19.4
8.9
34.7
5.7
4.0
July
7
M
10.8
12.3
23.4
18.9
4.9
53.7
5.0
7.3
July
8
26.1
M
13.4
22.2
21.5
45.7
83.0
7.3
13.2
July
9
13.1
M
19.1
36.0
16.7
48.7
75.7
27.0
25.3
July
10
M
M
20.8
25.9
22.8
21.0
M
M
10.6
July
11
M
M
14.2
27.6
46.6
28.2
M
3.5
2.7

M = Missing

Source = Environmental  Research and Technology7
                                      61

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                     TABLE 4.   STATION  NAMES,  TVA  NETWORK
                     (See Figure 5  for  station locations)
             1.  Allen
             2.  Bull Run
             3.  Colbert
             4.  Cumberland
             5.  Gallatin
             6.  John Sevier
             7.  Johnsonville
             8.  Kingston
             9.  DCAD  (Muscle  Shoals)
 10.   Paradise
 11.   Shawnee
 12.   Watts  Bar
 13.   Widows Creek
(14.) Giles  County
(15.) Hytop
(16.) Land Between Lakes
(17.) Loudon
(18.) Loves  Mill
(  ) B Rural  sampling site
                                   62

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TABLE 5.  SULFATE CONCENTRATIONS (ug/m3) TVA  NETWORK, JULY 3-11, 1974

Monitoring Site Data
Station
Allen
Allen
Allen
Bull Run
Bull Run
Bull Run
Col bert
Colbert
Col bert
Cumberland
Cumberland
Cumberland
Cumberland
Cumberland
Gal latin
Gal latin
Gallatin
John Sevier
John Sevier
Johnsonville
Johnsonville
Johnsonville
Johnsonville
Kingston
Kingston
Kingston
- Distances


.Distance1 Bearing Elevation
(Mi.) («) (Ft.)
4.2
2.9
3.2
2.6
4.9
4.3
1.8
2.3
2.4
4.3
6.2
1.1
4.6
19.2
1.8
4.2
4.8
1.9
1.0
2.6
2.8
2.6
2.1
3.6
2.9
1.3
and bearings


68
54
32
61
56
273
23
259
263
39
37
163
130
58
4
13
340
63
229
187
42
339
134
243
328
143
230
240
217
880
910
900
495
470
510
590
725
470
590
440
470
570
575
1220
1140
385
380
380
470
800
900
750
J
3 6
_
10.9
9.6
9.5
7.9
8.0
11.2
13.4
12.6
8.9
15.2
15.9
13.2
19.7
16.2
14.6
14.6
11.2
9.7
11.5
14.5
14.2
13.4
9.1
-
12.6
uly
789
8'.9
6.5
6.0



2.8
4.7
5.7
9.3
10.6
6.8
15.2
4.6
13.4
11.0
12.5


10.1
18.7
14.3
12.3



July 1974
Average
11.2
16.8
14.9
19.0
13.5
17.6
9.7
13.1
15.7
20.3
23.0
18.9
18.3
21.0
16.0
17.3
17.9
20.2
14.7
25.0
20.6
23.9
21.5
21.2
24.8
25.7
from power plant


(continued)
63







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TABLE 5.  (Continued)
Monitoring Site Data
Station
DCAD
DCAD
DCAD
Paradise
Paradise
Paradise
Paradise
Paradise
Shawnee
Shawnee
Shawnee
Shawnee
Watts Bar
Widows Creek
Widows Creek
Widows Creek
Widows Creek
Widows Creek
Giles County
Hytop
Land Between
the Lakes
Loudon
Loves Mill
Distance1 Bearing
(Mi.) (°)
1.5
1.2
2.4
2.6
2.9
7.9
5.3
21.0
2.6
2.6
2.7
2.1
0.8
2.5
4.8
2.0
2.0
2.3
10.0
19.3
35.8
6.5

224-
168
26
41
31
284
126
301
158
256
35
84
3
135
27
102
167
30
(NE)
271
320
(SSE)

Elevation
(Ft.)
530
510
550
420
490
460
398
475
375
360
385
350
845
1450
680
1500
1570
640
800
1785
580
880

3 6
13.1
22.3
19.5
17.1
20.0
18.2
16.2
17,3
13.6
14.7
16.3
14.6

20.4
31.8
30.1
28.6
31.4
15.6
16.1
12.7


July

July 1974
789 Average
11.2
15.8
13.0
17.0
17.7
15.0
16.7
20.4
14.5
13.5
15.5
10.2
12.1
19.0
M
31.1
26.5
24.9
17.0
10.2
10.9
9.7
5.9
18.2
19.8
31.5
24.8
25.5
26.7
20.0
28.8
29.5
27.7
27.7
25.9
24.1
23.0
24.0
33.2
29.7
26.4
16.0
15.5
21.1
23.2
14.8
             64

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                                   TECHNICAL REPORT DATA
                            (Please read Instructions on the reverse before completing)
 1. REPORT NO.
            EPA-600/4-79-009
                              2.
                                                           3. RECIPIENT'S ACCESSION-NO.
 4. TITLE AND SUBTITLE
    ASSOCIATION BETWEEN METEOROLOGICAL CONDITIONS AND
    HIGH  OZONE AND SULFATE CONCENTRATIONS
    A  1974 Episode in the Eastern  United States
             5. REPORT DATE
                February 1979
             6. PERFORMING ORGANIZATION CODE
 7. AUTHOR(S)
                                                           8. PERFORMING ORGANIZATION REPORT NO.
    Gerard A.  DeMarrais
 9. PERFORMING ORGANIZATION NAME AND ADDRESS
                (Same as Box  12)
                                                           10. PROGRAM ELEMENT NO.

                                                              1AA603    (FY-78)
                                                           11. CONTRACT/GRANT NO.
 12. SPONSORING AGENCY NAME AND ADDRESS
    Environmental Sciences Research Laboratory - RTP, NC
    Office of Research and Development
    U.S.  Environmental Protection  Agency
    Research Triangle Park, NC   27711
             13. TYPE OF REPORT AND PERIOD COVERED

                TnhniKiP  ?/7«-in/7ft	
             14. SPONSORING AGENCY CODE
                EPA/600/9
 15. SUPPLEMENTARY NOTES
 16. ABSTRACT
         A 1,000,000 km  area  of the Eastern United  States  had sulfate concentrations
    exceeding 10 yg/m  on July 10,  1974, and there were  indications that parts of
    the area had high concentrations on prior days.  The meteorology associated
    with the high concentrations and correlations of high ozone and sulfate concen-
    trations are discussed.   It appeared that slow moving and subsiding air contributed
    to the high concentrations of both pollutants.   Long range transport, as shown
    by trajectory analyses,  was a factor in the problems i.n most areas, but the worst
    situations with regards  to sulfates were associated  with emissions from nearby,
    upwind sources.  While high ozone concentrations were observed immediately
    prior to high sulfate concentrations in many areas,  there were high sulfate con-
    centrations that were not  associated with high ozone concentrations.  In the
    latter situation, the high sulfate concentrations  were  associated with air which
    had earlier movement over  areas with high S02 emission.
 7.
                                KEY WORDS AND DOCUMENT ANALYSIS
                  DESCRIPTORS
                                              b.lDENTIFIERS/OPEN ENDED TERMS
                           c. COS AT I Field/Group
    *Air pollution
    *0zone
    *Sulfates
    *Meteorological  data
  Eastern United States
  1974 episode
13B
07 B
04B
 8. DISTRIBUTION STATEMENT
                                              19. SECURITY CLASS (This Report)
                                                   UNCLASSIFIED
                           21. NO. OF PAGES
                                    75
                       RELEASE TO PUBLIC
20. SECURITY CLASS (This page)
     UNCLASSIFIED
                           22. PRICE
EPA Form 2220-1 (9-73)
                                            65

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