United States      Office of A ir Quality     ' EPA-450/3-78-110a
Environmental Protection  Planning and Standards     September 1978
Agency        Research Triangle Park NC 27711
Air                   ~~
The Development of
Mathematical Models for
the Prediction  of
Anthropogenic Visibility
Impairment

Volume I

-------
                                                  EPA-450/3/78-110a
                                Volume I


                  THE DEVELOPMENT OF MATHEMATICAL MODELS

                    FOR THE PREDICTION OF ANTHROPOGENIC

                           VISIBILITY IMPAIRMENT


                                   by
         Douglas A.  Latimer,  Robert W.  Bergstrom,  Stanley R.  Hayes
               Mei-Kao Liu, John H. Seinfeld, Gary Z.  Whitten
                   Michael  A.  Wojcik, Martin J.  Hillyer
                     Systems Application,  Incorporated
                       San Rafael,  California  94903
                            Contract 68-01-3947


       EPA Project Officers:  John Butler, David Shaver, James Dicke




                               Prepared for


                   U.  S.  ENVIRONMENTAL PROTECTION AGENCY

Office of Planning and Evaluation       Office of Air Noise and Radiation
401 M Street, SW                        Office of Air Quality Planning and
Washington, DC  20460                   Standards
                                        Research Triangle Park, NC  27711



                             September 1978

-------
                              DISCLAIMER
     This report has been reviewed  by the  Office  of Air Quality
Planning and Standards and the  Office of Planning and  Evaluation,
U.S.  Environmental Protection Agency and approved for publication.
Approval does not signify that  the  contents  necessarily reflect the
views and policies of the U.S.  Environmental Protection Agency, nor
does mention of trade names or  commercial  products constitute endorse-
ment or recommendation for use.

-------
                                  m
                         EXECUTIVE SUMMARY


     This three-volume report describes a nine-month study performed by
Systems Applications, Incorporated for the Environmental Protection Agency
to recommend and develop models that predict the contribution of manmade
air pollution to visibility impairment in Class I areas.  Two models were
developed:  One is a near-source plume model, based on a Gaussian formula-
tion, that is designed to compute the impact of a plume on visual range and
atmospheric coloration.   The other is a regional  model designed to calculate
pollutant concentrations and visibility impairment resulting from emissions
from multiple sources within a region with a spatial  scale of 1000 km on a
temporal scale of several days.

     The objective of this effort was to develop models that are useful pre-
dictive tools for making policy and regulatory decisions, for evaluating the
impacts of proposed new sources, and for determining the amount of emissions
reduction required from existing sources, as mandated by the Clean Air Act
Amendments of 1977.

     Both visibility models (plume and regional)  are based on atmospheric
dispersion models that account for the transport, diffusion, and surface
deposition of emissions  from point sources.   Concentrations of nitrogen
dioxide (N0?) are computed using a modified steady-state relationship;
sulfate and nitrate concentrations are calculated from S09 and NO  emis-
                                                         I-       A
sions using user-inputed pseudo-first-order rate constants.   The aerosol
size distribution is assumed to consist of four log-normally distributed
modes:  background submicron (accumulation), background coarse, plume
coarse (primary particulate),  and plume submicron (secondary particulate).
The effect of relative humidity on the mass of liquid water associated with
submicron aerosol is included  in the calculation  of aerosol  volume.   The

-------
                                   IV
spectral  light intensities at 39 wavelengths of light in the  visible spec-
trum are calculated for given lines of sight through the plume and the
background atmosphere by treating the plume as a homogeneous  layer and the
background atmosphere as two homogeneous layers.   The plume optical  thick-
ness is calculated taking into account the geometry of the plume and the
observer's line of sight.

     For a given line of sight, the spectral light intensities are used to
compute parameters that characterize visibility impairment, including vis-
ual range, luminance, chromaticity coordinates, contrast between plume and
background at various wavelengths, the blue-red luminance ratio, and a
parameter that characterizes plume perceptibility due to changes in both
light intensity and color.  These quantitative specifications of discolor-
ation can be translated to Munsell color notation so that a representative
color paint chip can be selected, thereby providing a subjective understand-
ing of the computed color.  Finally, with these color chips and a computer
graphics capability that displays perspective views of plumes and background
terrain, color illustrations of calculated atmospheric discoloration and
plume impact can be prepared.

     The plume model was applied to the hypothetical case of  a 2250 Mwe
coal-fired power plant emitting primary particulate, S09, and NO  at the
                                                       C.        A
maximum rates permitted by EPA's New Source Performance Standards.  Ambient
conditions typical of the Southwest were used in these calculations,
including a background visual range of 130 km (80 miles).  For an assumed
sulfate formation rate of 0.5 percent per hour, the plume's impact on
visual range was small near the source, but it increased with distance
from the source as sulfate aerosol was formed.  For neutral stability and
for sight paths perpendicular to the plume centerline, the calculated
visual range was reduced approximately 5 percent from the background value
at distances 200 to 300 km downwind of the power plant.  Except at short
downwind distances, where scattering is dominated by primary  particulate
(fly ash), sulfate formed in the atmosphere was the principal cause of
reductions in visual range.  The calculations, however, indicate that plume

-------
discoloration was caused principally by N02.  Yellow-brown plume discolor-
ation was most prominent during stable conditions at downwind distances of
40 to 100 km.  Light scattered by primary particulate and sulfate aerosol
tended to mask the discoloration due to N02; thus, control of particulate
and S02 emissions would increase discoloration.  Sulfate aerosol, by itself,
tended to cause a white plume (in forward scatter) or a grey plume (in back
scatter) when viewed against the horizon sky.

     The regional  model was applied to point source emissions of SO  in
                                                                   /\
the Northern Great Plains for two cases:   estimated 1975 emissions  of 430
tons/day and projected 1986 emissions of 1990 tons/day.   For a stagnation
episode characterized by light,  variable winds, the maximum reduction in
visual range was calculated to be 10 percent for the 1975 emissions and
25 percent for the 1986 emissions.   The most significant reductions in
visual range occurred hundreds of kilometers from the emissions sources.
For comparison, the impact of a  hypothetical complex of copper smelters
with a total SO  emissions rate  of 6000 tons/day (equivalent to the 1972
               /\
emissions from copper smelters in Arizona)  was evaluated with the Northern
Great Plains regional visibility model.  The maximum reduction in visual
range (for stagnation conditions) was calculated to be 50 percent and to
occur hundreds of kilometers from the sources.   Calculated maximum  sulfate
concentrations were in rough agreement with maximum sulfate concentrations
measured in nonurban locations in Arizona in 1972-1973.

     National Weather Service visual range  and meteorological data  for the
period 1948-1976 at 18 locations in the western United States were  analyzed.
Trends in visibility in Phoenix  and Tucson  were found to be correlated with
trends in SO  emissions from copper smelters.  During periods of copper
            A
strikes when smelter SO  emissions were eliminated, and during the  period
                       X
1973-1976 when SO  emissions from copper smelters were reduced from 6000 to
                 X
3000 tons/day, visibility improved.   The effect of smelter SO  emissions on
                                                             /\
visual range at distant nonurban locations  was evaluated by comparing visual
range frequency distributions at Prescott,  Winslow, and Farmington  during
the 1967-1968 copper strike with other periods.  Significant improvements

-------
in visibility during the copper strike were particularly associated with
winds that would transport smelter emissions directly to the given loca-
tions.

-------
                                    VII
                                CONTENTS



DISCLAIMER	     ii

EXECUTIVE SUMMARY 	    111

LIST OF ILLUSTRATIONS	     ix

LIST OF TABLES	xiii

LIST OF EXHIBITS	xiii

ACKNOWLEDGMENTS 	    xiv

DEDICATION	     xv

   I  INTRODUCTION  	      1

  II  THE NATURE OF VISIBILITY IMPAIRMENT 	      8

      A.  Definition of Visibility Impairment 	      8

      B.  Fundamental Causes of Visibility Impairment 	     17

      C.  Visibility Impairment in the Western United States  	     24

 III  THE ELEMENTS OF VISIBILITY MODELS	     35

      A.  Pollutant Transport, Diffusion, and Removal 	     35

          1.  Initial Dilution in a Buoyant Plume 	     37
          2.  Gaussian Plume Diffusion  	     39
          3.  Observer-Plume Orientation  	     40
          4.  Limited Mixing	     42
          5.  Plume Trajectory Box Model  	     42
          6.  Regional Transport and Diffusion  	     46

      B.  Atmospheric Chemistry 	     48

          1.  Conversion of NO to N02	     48
          2.  Conversion of Gases to Particles	     53

      C.  Aerosol Size Distribution	     57

      D.  Atmospheric Optics	•	     65

          1.  Calculation of the Scattering and
              Absorption Properties 	     65
          2.  Calculation of Light Intensity  	     71

-------
III   THE ELEMENTS OF VISIBILITY  MODELS  (continued)

     E.    Quantifying Visibility Impairment 	    75

          1.  Visual Range	    76
          2,  Contrast of Haze Layers and Plumes	    78
          3.  Color   	    81
          4.  Color Changes	    86

 IV   THE OUTPUT OF VISIBILITY  MODELS	    89

     A.    The Plume Visibility Model   	    90

     B.    Plume/Terrain Perspective Model  	   110

     C.    Color Display Techniques   	   113

          1.  Color Illustration  	   130
          2.  Color Video Display 	   136

     D.    The Regional Visibility Model  .....  	   138

  V   RECOMMENDATIONS FOR FUTURE  WORK	155

     A.    Impact Analysis in Support of Regulation  Development   .  .   156

     B.    Model Refinement and Testing	157

          1.  Model Testing	158
          2.  Gas-to-Particle  Conversion and Aerosol  Growth  ....   160
          3.  Assessment of Color Impact Thresholds 	   161
          4.  Refinement of Color Display 	   161
     C.    Model Validation	   163
          1.  The Type of Measurement Program	   163
          2.  Specific Measurements 	   165
          3.  Data Analysis, Assessment of Model  Performance,
              and Model Refinement   	   170

     D.    Further Data Analysis	   172
     E.    Development of a Southwest Regional  Visibility Model   .  .   174

REFERENCES	176

GLOSSARY	187

FORM 2220-1	193

NOTE	194

-------
                             ILLUSTRATIONS
 1    Outline of SAI's Study To Develop Models  for Predicting
      Visibility Impairment 	    4

 2    Elements and Potential Uses  of Visibility Models   	    6

 3    An Example of Reduced Visual  Range:   Marble  Canyon,  Arizona  ....   10

 4    An Example of Near-Source Visibility  Impairment:   Plume
      Discoloration Downwind of the Navajo  Generating Station
      in Northern Arizona  	   13

 5    An Example of Visibility Impairment:   A Uniform Haze
      Layer Visible from Bryce Canyon National  Park  	   14

 6    Natural Causes of Visibility  Impairment 	   16

 7    Effect of an Atmosphere  on the  Perceived  Light
      Intensity of Objects  	   21

 8    Map of the Western United States Showing  the Locations of
      Large Point Sources, Mandatory  Federal  Class I Areas, and
      NWS Stations Where Visibility Observations Are Made  	   26

 9    Frequency Distributions  of Extinction Coefficients Based
      on Visual Range Observations  at 13 Western U.S. Locations
      on Days Without Precipitation or Fog  in 1976	27

10    Dependence of Visual Range on Relative  Humidity at Four
      Locations in the Southwest	28

11    Historical Trends in Visibility in Phoenix,  Arizona  	   30

12    Percentage of Daylight Observations with  RH  < 60 Percent
      for Which Visual  Ranqe Exceeded 121 km, as a Function of
      Wind Direction, at Farmington,  New Mexico, 1949-1976  	  .   31

13    Schematic Logic Flow Diagram  of the Visibility Models 	   36

14    Gaussian Plume Visual  Impact  Model:   Observer-Plume  Geometry   ...   41

15    Plume Trajectory Box Model   	   43

16    Sensitivity of NO to N02 Conversion in  Power Plant Plumes
      to the Rate of Plume Dilution,  Background Ozone Concen-
      tration, and Solar Radiation	52

-------
17    Comparison of Measured N02/N0x Mole Ratios (Circled Points)
      in the Plume Centerline Downwind of a Coal-Fired Power
      Plant with Computer-Calculated Values (Solid Lines) Using
      Standard Pasquill  and Fitted or  	     54

18    Schematic of an Atmospheric Aerosol Surface Area Distri-
      bution Showing the Principal Modes, Sources of Mass
      for Each Mode, Process Involved in Inserting Mass in
      Each Mode, and Removal Mechanisms 	     58

19    Average Urban Model Aerosol Distribution Plotted in
      Five Different Ways	     59

20    Scattering-to-Volume Ratios for Various Size Distributions  ...     63

21    Ratio of Light Scattering to Mass as a Function of
      Relative Humidity 	     70

22    Light Scattering and Absorption in the Atmosphere 	     72

23    An Example of Plume Visual  Impact	     79

24    Chromaticity Diagram  	     82

25    Spectral Tristimulus Values x~(x), y(A), z"(x)	     84

26    Representation of a Color Solid	     85

27    Calculated Plume Visibility Impairment for a Hypothetical
      2250 Mwe Coal-Fired Power Plant with a Light Scattering
      Angle of 45° and Stability Class C	    100

28    Calculated Plume Visibility Impairment for a Hypothetical
      2250 Mwe Coal-Fired Power Plant with a Light Scattering
      Angle of 45° and Stability Class D	    101

29    Calculated Plume Visibility Impairment for a Hypothetical
      2250 Mwe Coal-Fired Power Plant with a Light Scattering
      Angle of 45° and Stability Class E	    102

30    Calculated Plume Visibility Impairment for a Hypothetical
      2250 Mwe Coal-Fired Power Plant with a Light Scattering
      Angle of 90° and Stability Class C	    103

31    Calculated Plume Visibility Impairment for a Hypothetical
      2250 Mwe Coal-Fired Power Plant with a Light Scattering
      Angle of 90° and Stability Class D	    104

32    Calculated Plume Visibility Impairment for a Hypothetical
      2250 Mwe Coal-Fired Power Plant with a Light Scattering
      Angle of 90° and Stability Class E	    105

-------
33    Calculated Plume Visibility Impairment for a Hypothetical
      2250 Mwe Coal-Fired Power Plant with a Light Scattering
      Angle of 180° and Stability Class C   	   106
34    Calculated Plume Visibility Impairment for a Hypothetical
      2250 Mwe Coal-Fired Power Plant with a Light Scattering Angle
      of 180° and Stability Class D	   107
35    Calculated Plume Visibility Impairment for a Hypothetical
      2250 Mwe Coal-Fired Power Plant with a Light Scattering Angle
      of 180° and Stability Class E   	   108
36    Observer Locations for Plume-Terrain Perspective Views   	   112
37    View from Location 1   	   114
38    View from Location 2	   115
39    View from Location 3	   116
40    View from Location 4	   117
41    View from Location 5	   118
42    View from Location 6	   119
43    View from Location 7	   120
44    View from Location 8	   121
45    View from Location 9	   122
46    View from Location 10	   123
47    View from Location 11	   124
48    View from Location 12	   125
49    View from Location 13	   126
50    View from Location 14	   127
51    View from Location 15	   128
52    Schematic Showing Color Display Techniques  	   129
53    Photocopy  of the Power Plant Plume in Northern.Arizona
      Selected for Simulation 	   132

-------
                                   xii


54    Photocopy of the Perspective Terrain View with Calculated
      Munsell Color Notation and Corresponding Color Chips  	    134

55    Photocopy of Color Illustration Created by an
      Artist from Indicated Munsell Color Chips 	    135

56    Photocopy of a Color Video Display of Plume Visual  Impact -  .  .  .    137
                                                                    O
57    Predicted Regional Three-Hour-Average SO? Concentrations (pg/m )
      Based on 1986 Emissions in the Northern Great Plains for the
      Meteorological Conditions of 1400-1700 MST on 6 April  1976.  ...    140

58    Predicted Regional Three-Hour-Average N0£ Concentrations (ppb)
      Based on 1986 Emissions in the Northern Great Plains for the
      Meteorological Conditions of 1400-1700 MST on 6 April  1976  ...    141

59    Predicted Regional Three-Hour-Average Sulfate Concentrations
      (pg/mj), Assuming a 0.5 Percent per Hour Sulfate Formation Rate,
      Based on 1986 Emissions in the Northern Great Plains for the
      Meteorological Conditions of 1400-1700 MST on 6 April  1976  ...    142

60    Predicted Regional Visual Range (km), Assuming a Background
      Visual Range of 130 km and a 0.5 Percent per Hour Sulfate
      Formation Rate, Based on 1986 Emissions in the Northern Great
      Plains for the Meteorological Conditions of 1400-1700
      MST on 6 April 1976	    143

61    Predicted Regional Three-Hour-Average S02 Concentrations
      (yg/m3) Based on Hypothetical Copper Smelter Emissions
      for the Meteorological Conditions of 1400-1700 MST on
      6 April 1976 in the Northern Great Plains	145

62    Predicted Regional Three-Hour-Average Sulfate Concentrations
      (yg/m^), Assuming a 0.5 Percent per Hour Sulfate Formation
      Rate, Based on Hypothetical Copper Smelter Emissions for
      Meteorological Conditions of 1400-1700 MST on 6 April  1976
      in the Northern Great Plains	    146

63    Predicted Regional Visual Range (km), Assuming a Background
      Visual Range of 130 km and a 0.5 Percent per Hour Sulfate
      Formation Rate, Based on Hypothetical Copper Smelter Emissions
      for Meteorological Conditions of 1400-1700 MST on 6 April 1976
      in the Northern Great Plains	    147

64    Predicted Regional Visual Range (km), Assuming a Background
      Visual Range of 130 km and a 0.3 Percent per Hour Sulfate
      Formation Rate, Based on Hypothetical Copper Smelter Emissions
      for Meteorological Conditions of 1400-1700 MST on 6 April 1976
      in the Northern Great Plains	    149

65    Predicted Regional Visual Range (km), Assuming a Background
      Visual Range of 130 km and a 1 Percent per Hour Sulfate Formation
      Formation Rate, Based on Hypothetical Copper Smelter Emissions
      for Meteorological Conditions of 1400-1700 MST on 6 April 1976
      in the Northern Great Plains	    150

-------
                                  xiii
                                TABLES
1    Main Milestones in Visibility Protection Regulation  	    2

2    Percent Reduction in Visual  Range by Three Levels
     of S0? Emissions	45

3    Measured Size Distributions  of Atmospheric Aerosol   	  62

4    Estimates of Extinction Coefficients per Unit Mass   	  67

5    Mean and Maximum 24-Hour-Average Sulfate Concentrations
     Measured in Arizona in 1972-1973  	  151
                               EXHIBITS
1    Sample Plume Model  Output:   Input Emissions
     and Ambient Conditions	,	91

2    Sample Plume Model  Output:   Pollutant Concentrations   	  93

3    Sample Plume Model  Output:   Visual  Effects for
     Horizontal  Sight Paths  	  95

4    Sample Plume Model  Output:   Visual  Effects for
     Nonhorizontal Sight Paths 	  97

5    Sample Plume Model  Output:   Visual  Effects for
     White, Grey, and Black Backgrounds   	  98

6    Example of  Visual  Effects at a  Given Location  in  a
     Region with 2 ug/nr S0= and 30  ug/m3 Coarse  Particulate  	 153

-------
                                 XIV
                            ACKNOWLEDGMENTS
     Many people inside and outside  of  SAI  have assisted us in this
work.  At SAI we particularly  want to thank Gary Lundberg for his
excellent computer work and Shep  Burton for his guidance.  The support
of John Butler, David Shaver,  James  Dicke,  John Bachmann, Steve Eigsti,
Joseph Tikvart, Terry Thoem, and  Donald Henderson of the EPA is greatly
appreciated.  We thank Donald  LaBash for his  color  illustrations and
Ellen Leonard and Michael  Williams of Los Alamos Scientific Laboratory
for their help with the color  video  display techniques.  Also, we grate-
fully acknowledge the conversations  and helpful suggestions of George
Hidy, Robert Charlson, John Trijonis, Thomas  Peterson, William Wagner,
and Edwin Roberts.

-------
                              XV
                        DEDICATION
We dedicate  this report to the memory of Terry N. Jerskey.

-------
                            1   INTRODUCTION


     The Clean Air Act was amended in August 1977 to contain  a  section
requiring the restoration and protection of visibility in national  parks,
wilderness areas, and forests that have been classified as mandatory  Class  I
federal areas.*  In that section Congress boldly declared "as a national
goal the prevention of any future, and the remedying of any existing
[our emphasis], impairment of visibility in mandatory Class I Federal
areas which impairment results from man-made air pollution."  Furthermore,
Congress defined "impairment of visibility" as  a reduction in visual  range,
an atmospheric discoloration, or both.

     Although many sources of air pollution cause or contribute to  vis-
ibility impairment, including vehicular emissions from urban  areas  and
sulfur dioxide emissions from copper smelters,  Congress was particularly
concerned with the alleged impact of power plant emissions on the magnif-
icent vistas in national parks such as the Grand Canyon and Bryce Canyon.
The 1977 Clean Air Act Amendments require that  the foil owing  action be
taken (see Table 1):

     >  The Department of the Interior, in conjunction with the
        Environmental Protection Agency (EPA),  must identify  all
        mandatory Class I areas where visibility is deemed to be
        aesthetically important.
     >  The EPA must report to Congress on the  emissions sources
        and the air pollutants that cause or contribute to visibil-
        ity impairment, on recommended methods  of measuring
* Section 128 of Public Law 95-95 amends  Part C  of Title  I of  the  Clean
  Air Act by adding Section 169A concerning  "visibility protection for
  Federal Class I areas."

-------
      TABLE 1


    Date

August 1977
February 1978
August 1978
February 1979
August 1979
MAIN MILESTONES IN VISIBILITY PROTECTION REGULATION
	Milestone	

Congress passed the 1977 Clean Air Act Amendments
containing Section 169A on visibility protection:
"Congress hereby declares as a national goal the
prevention of any future, and the remedying of any
existing, impairment of visibility [defined as a
 'reduction in visual range1  or an  'atmospheric
discoloration'] in mandatory Class I Federal areas
which  impairment results from manmade air pollution"

Department of Interior is required to identify all
mandatory Class I areas where visibility is an impor-
tant aesthetic value

EPA is required to promulgate a list of mandatory
Class  I federal areas where visibility is an important
aesthetic value

EPA is required to report to Congress recommending
methods to characterize visibility in Class I areas,
modeling techniques (or other methods) for determining
the impact of man-made air pollution on visibility, and
methods to prevent and remedy air pollution

EPA is required to promulgate regulations requiring
states to "make reasonable progress" toward preventing
and remedying visibility impairment, including use of
the best available retrofit technology for point sources
less than 15 years old and development of a 10 to 15
year long-term strategy

-------
        visibility impairment in Class I areas,  on recommended
        modeling techniques for determining the  contribution of
        man-made air pollution to visibility impairment in Class  I
        areas, and on methods for preventing and remedying such air
        pollution.
     >  The EPA must promulgate regulations that ensure reasonable
        progress toward meeting the national visibility goal.

     It is clear that Congress intended that existing sources  be  controlled
so that visibility would not be significantly impaired in Class I areas.
Each existing major stationary source less than  15 years old that emits
an air pollutant that causes or contributes to any Class I area visi-
bility impairment is required to procure, install, and operate the  "best
available retrofit technology" for controlling air pollutant emissions
"as expeditiously as possible."  However, the Environmental  Protection
Agency may exempt a source from this retrofit requirement on the  grounds
that the source does not emit pollutants that cause or contribute to
significant visibility impairment in Class I areas.  Although  the main
focus of the visibility protection section (No.  169A) is on existing
sources, other sections of the 1977 Clean Air Act Amendments require
that new-source reviews demonstrate that the emissions from a  proposed
major facility do not cause "an adverse impact on the air quality related
values (including visibility)" of Class I areas.

     This report describes a nine-month study performed by Systems
Applications, Incorporated (SAI) for the Environmental Protection Agency
to recommend and develop models that predict the contribution  of  man-
made air pollution to visibility impairment in Class I areas.   As shown
in Figure 1, this study was divided into three main phases,  consisting
of seven tasks:

     >  Model formulation
        -  Recommendations for modeling approaches.
        -  Collection and analysis of data to characterize
           existing visibility impairment.

-------
oo

§
crt LU
_l V)
Q
ii

o z
< o
O. —
zi-


^i
CO O
>
0<
OZ
Q>—
                          I UJ
                         zo
                         oz
                         O UJ O
            Ul< XZ
            —   t— t—
            0:0    <
                o:
            uj   o   r
            Q CO *— — I O
                    < —
                                              a
                                              z
                                             2  3Z
                                             o  a- r>
                                             o   •>
                                             o  tea
    o    o    o
co  o    cr co  cr
Ul  —CO  19 Z  19
I-  >- z  :*o  *
<  cr o  o—  o
cr  < —      cr
o  >- m  >- \-  t-
                                                        ei  o o
                                                        iC     UJ
                                                        (_>  u. -5
                                                        <  Oca
                                                        CO     O

                                                        CO  CC to
              oui
              z_l
                 o
                                    CO
                                        < cr  uj LU  ui
                                        ZH-  —o  —
              a: a.
              t- i
              to o
                         — z to<
                       >- to O — CT
                       _! O
                       Q- — I-    _l
                       O-Z — ZO
                       < UJO O O
                          ui  a. a  < o
    Ul  O Ul  LU CO

    —  LU—  X<

    >  19 >  OO
           t
Q_
O
                              I    I—
                              cr   cr
                              Ocoo

                                I UJ CO
                                 •iz J .
                                   < UJ
                                                                                    z o
                                                                                    — co
                                                                                       o
                                                                                    to a:
                                                                                    Ul UJ
                                                                                                        < —
                                                                                  — ouj
                                                                                  >   IT Z
              UJ—   ~
              K
o ui z
z x o
— i- o
                                                     ~ to uj
                                                     CO OQ
3CO
O UJ
LU I— CO
a
< cr i_
  UJ Q
Z X<
< h-:
                                                                                                        QUJ<
                                                                      C£
                                                                      H^


                                                                      a.
                                                                                                                               co
                                                                                                                               h—t
                                                                                                                               00
                                                                                                      coo —
                                                                                                      O U- QQ
                                       _
                                       Ul   <
                                       Q   a-
                                       O   Z
                             to  o
                             —  co
                             >   i
                                               i  z
                                               _iui
                                               
                                           o
                                           o
                                     cr


                                     I
                                     o
                                     o
                    Qa:
                    zo
                                     oco
                                     o.
                     tu.     U.  H-
                          cr u.  i

                          o
cr    —I
    u.o
co  oo
to
<  ZO
£  o —
i   —cr
o  i-ui
i-  < x
i   -lo-
  K 3UI —
                                                                        QQ>  COZ
                                                                                                                                          UJ
                                                                                                                                          QE:


                                                                                                                                          CD
                                                                                                                                          I—I
                                                                                                                                          u_

-------
     >   Model  development
        - Near-source  plume visibility  model.
        - Regional,  multiple source  visibility model.
     >   Model  applications
        - Documentation of  models.
        - Application  of models  to typical  emission, meteoro-
          logical,  and ambient conditions.
        - Recommendations for further work.
        - Information  for the Report to Congress.

     Two basic types of models were  developed for the  prediction of
visibility impairment caused by  anthropogenic pollutant emissions.   One
is a near-source plume model, applicable to a wide range of emission,
meteorological, and ambient conditions, that is  based  on a Gaussian
formulation.  This  model is designed to estimate plume concentrations
and visual effects  on a spatial  scale of up to 350 km.  The other is a
regional-scale model designed to estimate pollutant concentrations  and
visual  effects in the Northern Great Plains over a spatial scale of 1000 km.
Both models calculate the reduction  in  visual range and the atmospheric dis-
coloration resulting from directly emitted primary particulate matter and
from nitrogen dioxide, sulfates, and nitrates formed in the atmosphere
from pollutant precursors.

     The goal  of this development is models that are useful predictive
tools for makinq policy and regulatory  decisions, for  evaluating the
impact of proposed  new sources,  and  for determining the amount of emissions
reduction required  from existing sources.  Figure 2 shows the  elements
and potential  uses  of visibility models.  The critical decisions that
must be made in the future  regarding the definition of "significant
visibility impairment" cannot be made without a  basic  understanding of
the implications for enforcement in  new and existing source reviews, and,
in particular, the  impact on energy  development  in the western United
States.  We believe that visibility  issues will  have a significant
influence on the siting and design of new coal-fired power plants in

-------An error occurred while trying to OCR this image.

-------
the West and on the evaluation of retrofit requirements for existing
plants.  Thus, modeling of visibility impairment is  likely to become  an
integral part of the environmental  assessment of new and  existing  sources,
providing a basis for major siting  and pollution control  decisions in
the future.

     This report contains five chapters and seven appendices.  Chapter II
discusses the nature of existing visibility impairment in Class I  areas,
with particular emphasis on the western United States.  The elements  of  the
visibility models are discussed in  Chapter III, and  a summary of the  plume
and regional models and their output is given in Chapter  IV.   Chapter V
discusses our recommendations for future work.  Appendix  A presents the
details of our analysis of visibility data in the western United States,
and Appendix B, the details of the  atmospheric optics calculations.
Appendix C discusses sulfate formation in the atmosphere, Appendix D
describes the plume model, and Appendix E shows plume model calculations
and the results of a sensitivity analysis.  Appendices F  and  G describe
the Northern Great Plains regional  model and calculations for seven
scenarios.  The appendices are bound separately in Volume II.  Volume III
presents a  series  of case  studies of  power plant plume visual  impact for
a number  of emission, meteorological,  and ambient background scenarios.

-------
                                     8
           II   THE NATURE OF  VISIBILITY  IMPAIRMENT
      "Visibility impairment"  must  be  defined  before discussing the components
of the mathematical  models used to  predict  anthropogenic visibility impair-
ment and the specific plume and regional  visibility models developed as a part
of this study.  This chapter defines and  classifies "visibility impairment"
by type, magnitude,  spatial and temporal  extent,  and cause, and it provides
examples of visibility impairment.  The fundamental physical concepts of
visibility impairment are also briefly discussed,  and  the analysis of visual
range data from the Southwest and the  Northern Great Plains is summarized;
this material is presented in more  detail  in Appendix  A.

A.  DEFINITION OF VISIBILITY IMPAIRMENT

      "Visibility impairment" has been defined generally by Congress in the
Clean Air Act Amendments of 1977 as a  "reduction  in visual range" or an
"atmospheric discoloration," but the term must be defined more precisely and
illustrated by examples before we discuss the  models and quantitative speci-
fications of visibility impairment.

      Visibility impairment can be  defined and classified according to:

      >  Type (e.g., the appearance of distant objects, general hazi-
         ness, yellow-brown or grey discoloration).
      >  Magnitude (e.g., visual range, degree of coloration, contrast,
         "any" or "significant" impairment of  visibility in the termin-
         ology of the Clean Air Act Amendments).
      >  Spatial extent (e.g., localized plume appearance, uniform haze,
         distance downwind of source).
      >  Temporal extent (frequency of occurrence of reduced visual
         range or of discoloration).

-------
      >  Location relative to Class  I  areas  (impact  on  a  vista  from
         a Class I area or on a  vista  looking  into a Class  I  area).
      >  Cause (natural or man-made  aerosols of coarse  particulate
         matter, sulfate, nitrate, organics, soot, or nitrogen
         dioxide gas).

      The term "visibility" is generally used  synonymously  with "visual
range," meaning the farthest distance  at which one can  see  a  large,  black
object against the sky at the horizon.   One  can make subjective evaluations
of "visibility" every time he views  objects  outdoors.   Although large
black objects are not generally available for  observing and evaluating
visual range, dark objects such as buildings,  TV towers,  hills, or mountains
can be viewed against the horizon sky.

      Even if no distant objects are within  view, subjective  judgments  about
visual range can be made by noting the coloration and light intensity of the
sky and nearby objects.  For example,  one perceives  reduced visual range if
a distant mountain that is usually visible cannot be seen,  if nearby objects
look "hazy" or have diminished contrast, or  if the sky  is white, grey,
yellow, or brown rather than blue.

      Figure 3 shows an example of reduced visual range in  Marble Canyon in
northern Arizona.  As shown by this  photograph, reduced visual  range is
detectable because the distant walls of the  canyon are  difficult to  distin-
guish.  The contrast between the given object  (part  of  the  canyon) and  the
background (the horizon or a more distant terrain feature)  is reduced by
light scattered from particles in the  intervening atmosphere.  Also, even
if terrain features were not visible,  the intensity  and the yellowish
coloration of the scattered light would degrade the  aesthetic quality of the
atmosphere.  Many of the Class I areas (e.g.,  national  parks, national
forests, wilderness areas) were  so designated  because of  their  scenic views
of such distant terrain features as  mountains, canyon walls,  plateaus,  and
buttes.  Indeed, in the western  United States, where most of  the Class  I
areas are located, spectacular scenery is enhanced by generally excellent
visibility, which makes the colorful terrain features stand out with great

-------
10
                                  o
                                  o
                                  >-

                                  •a:
                                  o

                                  UJ
                                  _l
                                  CO
                                  cc:





                                  UJ
                                  C3


                                  1

                                  _i
                                  <

                                  oo
                                  i—i
                                  >

                                  o
                                  LU
                                  O

                                  O
                                  LU
                                  C£

                                  U_
                                  O

                                  LU
                                  	I
                                  0_

                                  
-------
                                   11
clarity.  However, even in flat areas (e.g.,  the Big Sky Country  of the
Northern Great Plains), a slight reduction in visual range or a  slight
atmospheric discoloration can change what originally appeared to  be an
"infinite" horizon to a less desirable white, yellow, grey, or brown
horizon.

     The magnitude of impairment can be characterized by the reduction in
visual range from some reference value, by a  reduction in contrast between
an object and the horizon sky at a known distance from the observer, or  by
a shift in coloration or light intensity of the sky or distant objects,
such as clouds or terrain features, compared  with what is perceived on a
"clear" day.  In all  cases, the magnitude of  visibility impairment can be
characterized by the change in light intensity or coloration of an object
(or part of the sky)  compared with that of some reference object.   For
example, a distant mountain is visible because the intensity and  coloration
of light from the mountain is different from  that of the horizon  sky.
Another example is a plume or haze layer seen against the background sky
or terrain features.   The pollution is visible only if the light  intensity
or coloration of the plume contrasts with that of the surrounding sky or
terrain.

     The most subjective impairment observation occurs when an observer
compares the appearance of the sky or distant terrain features on a hazy
day with recollections of what it was on a clear day in the past.   Exam-
ples of such subjective comparisons are those of old-timers who recall
that visibility used to be much better.  Although these observations can-
not be discounted entirely, it is possible that such judgments may be the
result of nostalgia or poor memory.

     The spatial extent of visibility impairment is important to  both the
perception and the significance of impairment to observers in Class I
areas.  The sensitivity of an observer to brightness and color differences
between two objects depends on the geometric  relationship between the
objects.  If each of the objects is uniformly colored and there  is a sharp

-------
                                     12
line of demarcation between the objects,  such as  when  a  mountain  is  viewed
against a horizon sky, a smaller change in light  intensity  or  color  can
be perceived than if the boundary between the two objects is vague,  as in
the case of a plume viewed against the horizon sky.   If  the observer is
located in a uniformly colored atmosphere, atmospheric discoloration is
perceived, not by comparison of two colored fields,  but  by  comparison
with his recollection of a clear atmosphere.

     Figure 4 provides an example of near-source  visibility impairment.
The spatial extent of visibility impairment is defined by the  dimensions
of the plume.  The plume is visible because the light  intensity and  color
of the plume are different from those of  the clouds  in the  background.
Because of the resultant relatively sharp boundary between  the plume and
the background, the visual impact on the  observer is dramatic.  Figure 5
shows another example of the importance of the spatial extent  of  impair-
ment on its perceptibility.  In that photograph,  the haze layer is clearly
visible because of the sharp demarcation  line between  it and the  layer of
clean air above it.

     The temporal extent (or the frequency of occurrence) of visibility
impairment) is of great importance in determining the  acceptability  of air
pollution levels.  The frequency of occurrence of impairment could be char-
acterized by stating the number of days or hours  in  a  year  that the  magni-
tude of visibility impairment is greater  than some standard.   Using  these
data, one might state that at a given location it is acceptable for  visual
range to be less than y km for x percent  of the daylight hours.

     The location of visibility impairment is extremely  important in terms
of visibility protection legislation because the  law states that  only the
visibility in Class I areas is to be protected and restored.   We  assume  that
this definition can include impairment caused by pollution  outside of a
Class  I area that  is visible within a Class I area.   In  areas  with excel-
lent background visibility, visual degradation perceived by an observer  in
a Class I area could be caused by pollution many kilometers away.  It is not

-------
13
                                      LU Z
                                      SO
                                      0-j.C

                                          oo
                                      l—l CtL

                                      - o

                                      •~2

                                      S$
                                      i—i ^
                                      CO Z
                                      I—I
                                      OO LU
                                      i—i I
                                      > I—

                                      LU U_
                                      O O

                                      •=> c*
                                      o z
                                      00 H-I
                                       i  3  <;

                                         S3  O
                                         O  M
                                      Z Q  i-t
                                             OH
                                      Lu Z  ct
                                      O O

                                      LU £  o:
                                      _J 
-------
14
                                        a:
                                     OL.
                                     O
                                     2: o
                                     H- o
                                     z >-
                                     o: o
                                     I— I
                                     c£ LU
                                     D- U
                                     s: >-
                                     i— i OL
                                        CO
                                     CO
                                     i— i LU
                                     (/) _J
                                     1-1 CQ
                                     Q- >-
                                     S «C
                                     < —I
                                     X
                                     LU LU
                                        M
                                     LO

                                     LU
                                     o:
                                     =5
                                     C3

-------
                                     15
clear whether Congress meant to protect the visibility in Class I  areas
from such distant pollutants.

     Finally, perhaps the most important classification of visibility
impairment is by cause, in particular,  whether the cause is natural  or
anthropogenic sources.  Clearly, Congress has been concerned only  with
anthropogenic visibility impairment.   Reductions in visual  range caused
by precipitation, fog, clouds, windblown dust, sand, snow,  or "natural"
aerosol  are natural  occurrences and cannot be controlled by man.   Indeed,
some natural visibility impairment may  contribute to the enjoyment of
Class I  areas.   Examples of such phenomena are  the  blue  haze of the Great
Smoky Mountains and the fog and hazes along the California  and  Oregon
coast.

     Assessment of anthropogenic contributions to visibility impairment
can be difficult when background visibility varies spatially and temporally
and when natural atmospheric constituents interact with anthropogenic
emissions to create a combined effect,  such as that of the  haze formed
when anthropogenically emitted hygroscopic particles absorb liquid water
in the atmosphere.  For the purpose of  discussion only, the Venn diagram
in Figure 6 shows the frequency of occurrence of  visibility  impairment,
which is defined here as visual range less than 80 km (50 miles).   Some
natural  causes  of visibility impairment, such as windblown  dust, precip-
itation, fog, and cloud cover, are represented by circles whose total
areas and areas of overlap represent the frequency of occurrence of the
given phenomenon and the associations among phenomena.   Note in Figure 6
that fog always causes visibility impairment and precipitation  usually
does.   In  this  highly schematic representation,  the  diagonally lined  area
 represents  the  fraction of time that man-made emissions  cause or  contribute
 to  visibility "impairment.   In  actual situations,  it  is  difficult  to sep-
 arate the  relative  magnitude's  of  natural  and man-made  contributions to

-------
                                                          16
oo
z
o
*— i

«=c

a;
CD
O
                                                                                                              CQ
                                                                                                              »— H

                                                                                                              oo
                                                                                                              o

                                                                                                              
-------
                                      17
visibility impairment.   For example,  as noted above,  during  humid  condi-
tions, natural  and anthropogenic hygroscopic  particles  may absorb  water,
thereby causing visibility impairment.   Because  the atmosphere  is  a  complex
system consisting of both natural  and anthropogenic aerosol,  the contribu-
tion of man-made pollution to visibility impairment may be difficult to
characterize by measurements.  The causes of  visibility impairment are dis-
cussed in further detail  in the sections below from both fundamental  and
phenomenological viewpoints.

B.   FUNDAMENTAL CAUSES OF VISIBILITY IMPAIRMENT

     Visibility impairment is caused  by the following interactions in the
atmosphere:

     >  Light scattering
        -  By molecules of air
        -  By particles
     >  Light absorption
        -  By gases
        -  By particles.

Light scattering by gaseous molecules of air  (Rayleigh  scattering),  which
causes the blue color of  the atmosphere,  is  dominant when the air is rela-
tively free of aerosols and light-absorbing gases.  Light scattering by
particles is the most important mechanism causing reductions  in visual
range.  Fine solid or liquid particulates whose  diameters range from 0.1
to 1.0 ytn (the most effective size per unit mass in scattering light)
account for most of atmospheric light scattering.  Light absorption  by
gases is particularly important in the discussion of  anthropogenic visi-
bility impairment because nitrogen dioxide, a major constituent of power
plant plumes, absorbs light.  Nitrogen dioxide is reddish-brown because
it absorbs strongly at the blue end of the visible spectrum while  allowing
light at the red end to pass through.  Light  absorption by particles is

-------
                                      18
important when black soot (finely divided carbon)  is  present.   However,
most atmospheric particles are not generally considered to  be  light
absorbers.

     Anthropogenic contributions to visibility impairment result  from the
emission of primary particulate matter (such as fly ash, acid, or water
droplets, soot, and fugitive dust) and of pollutant precursors that are
converted in the atmosphere to the following secondary species:

     >  Nitrogen dioxide (NCL) gas, from emissions of nitric
        oxide (NO).
     >  Sulfate (SOp particles, from SOX emissions.
     >  Nitrate (NO:;) particles, from NOV emissions.
                   O                    X
     >  Organic particles, from hydrocarbon and NO  emissions.
                                                  X

Before particulate control technology was commonly employed,  primary par-
ticulate matter, such as smoke, windblown dust, and soot, was  a major con-
tributor to visibility impairment.  Coal-fired power plants emit  primary
particles of fly ash and combustion-generated particulates  to  the atmo-
sphere.  If such plants are equipped with efficient precipitators or other
abatement equipment, the emission rate of primary  particles may be small.
However, some emissions escape the control equipment and do contribute
to the ambient particulate concentration and hence to general  visibility
impairment.  If the emission rate of primary particulates is sufficiently
large, the plume itself may be visible.

     In the past, many of the older coal-fired power plants generated
conspicuous, visible plumes resulting from the large emission rates of
primary particulate matter.  Old plants still in operation and newer plants
have benefited from more efficient particulate abatement equipment and a
state-of-the-art that has reached the point where particulate removal
efficiencies in excess of 99 percent are commonly specified and achieved.
In addition, with  the installation of flue gas desulfurization systems
(scrubbers) and with boiler combustion modifications, sulfur dioxide and

-------
                                    19
nitrogen oxide emissions have also been reduced.   As a  result,  the visual
impact of power plant plumes has been sharply reduced,  as  evidenced by
the nearly invisible plumes of modern coal-fired  power  plants.   Unfor-
tunately, however, the contribution to visibility impairment  of the
secondary pollutants—nitrogen dioxide gas and sulfate,  nitrate,  and
organic aerosol--is now becoming increasingly evident and  is  of growing
concern.

     Since nitrogen dioxide absorbs light selectively,  it  can discolor
the atmosphere, causing a yellow or brown plume when present  in sufficient
concentrations.  Almost all of the nitrogen oxide emitted  from  power plant
stacks is nitric oxide, a colorless gas.   But chemical  reactions  in the
atmosphere can oxidize a substantial  portion of the colorless NO  to the
reddish-brown N(L.

     Secondary sulfate, nitrate, and  organic particles  have a dominating
effect on visual range in many situations because these  particles range  in
size between 0.1 and 1.0 ym in diameter,  which is the most efficient size
per unit mass for light scattering.   As is noted  later,  submicron aerosol
(with diameters in the range from 0.1  to  1.0 ym)  is 10  times  more effec-
tive in light scattering than the same mass of coarse (> 1 ym)  aerosol.
Also, because secondary aerosol forms slowly in the clean  atmospheres
typical of Class I areas in the western United States,  maximum  aerosol
concentrations and associated visibility impairment may occur at large
distances from emissions sources.  We discuss this problem further in
Section C, which concerns visual range observations in  the West,  and in
the chapters that describe the models.

     The effect of the intervening atmosphere on  the visibility and colora-
tion of a viewed object (e.g., the horizon sky, a mountain, a cloud) can
be calculated by solving the radiation transfer equation along  the line of
sight.   As we noted in Section A, visibility impairment  can be  quantified
by comparing the intensity or the coloration of two objects (e.g., a distant

-------
                                    20
mountain against the horizon sky).   The effect of the  intervening  atmosphere
on the light intensity, as a function of wavelength,  of the  viewed  object  can
be determined if the concentration  and characteristics of air  molecules,
aerosol, and nitrogen dioxide are known along the line of sight.

     The change in spectral light intensity I (A)  as  a  function of  distance
along the sight path at any point in the atmosphere, neglecting multiple
scattering (see Figure 7), can be calculated as:
where
              r = the distance along the sight path from the  object
                  to the observer,
           p(0) = the scattering distribution function for scattering
                  angle 0 [see glossary and Figure 7(a) for definitions],
                                         2
             F  = the solar flux (watts/m ) incident on the atmosphere,
          bp,. = the sum of the Rayleigh scattering (due to  air
           sea L
                  molecules) and the scattering due to particles:

                            bscat(x> = bR(x) and bsp(x)    •         {2)

           b   . = the sum of the scattering and absorption coefficients:

                           bext'x) ' bscat + babs    •         (3)

     On the right-hand side of Eq. (1), the first term represents  light
absorbed or scattered out of the line of sight; the second term represents
light scattered into the line of sight.  The values of bscat  and bext can
be evaluated if the aerosol and NOp concentrations and such characteristics
as the refractive index and the size distribution of the aerosol are known.
Except in the cleanest atmospheres, b •   .  is dominated by b  :  also,  unless
                                     SCuU                  Sp
soot is present, b .   is dominated by the absorption coefficient due to

-------
            SUN
                   vZENITH
                     .ANGLE
          SCATTERING
          ANGLE e
OBJECT
 ELEMENTAL VOLUME
 .(CONTAINING AIR,
/PARTICLES, AND N02)
                                        /INE OF  SIGHT


                                    + dl
                        OBSERVER
                       (a)  Geometry
       LIGHT INTENSITY OF HORIZON
                      Object-Observer Distance r
      (b)  Visual  Range r  (Homogeneous Atmosphere)
FIGURE 7.   EFFECT OF AN ATMOSPHERE  ON THE PERCEIVED.  LIGHT
            INTENSITY OF OBJECTS

-------
                                    22
N02-   Scattering and absorption are wavelength-dependent,  with  effects
being largest at the blue end (A =  0.4 pm)  of the  visible  spectrum
(0.4 < x < 0.7 pm).   The Rayleigh scattering coefficient bD  is  propor-
           -4
tional to A  ; the scattering coefficient caused by particles  is  generally
proportional  to A~n, where 1  < n <  2.   Also, N02 absorption  is  greatest  at
the blue end.  This  wavelength dependence causes the coloration of the
atmosphere.

     For a uniform atmosphere, without inhomogeneities  caused  by  plumes
(where b   .  and b  t do not vary with r),  Eq. (1) can  be  solved  to find
the intensity and coloration of the horizon sky:
                                                                    (4)

The perceived intensity of distant bright and dark objects will  approach
this intensity as an asymptote, as illustrated by Figure 7(b).

     The visual range rv is the distance at which a black object is barely
perceptible against the horizon sky, which occurs when the perceived light
intensity of the black object is (1 - C -n)Iu» where  C.  is the liminal
(barely perceptible) contrast, commonly assumed to be 0.02.   When Eq.  (1)
is solved for r , for a uniform atmosphere, ry is independent of p(0)  and
FS(A) and can be calculated using Koschmieder's equation:
                       r  .
                          '
where bext(A) ">s evaluated at the middle of the visible spectrum (to which
the human eye is most sensitive) and where A = 0.55 ym.  The visual  range
for a nonuniform atmosphere  must be calculated by evaluating Eq.  (1) for
the appropriate  conditions of the given situation.

     Atmospheric  coloration  is  determined  by  the wavelength-dependent
scattering  and  absorption  in the atmosphere.  The spectral distribution

-------
                                      23
of I(A) for x over the visible spectrum determines the perceived color
and light intensity of the viewed object.   The relative contributions of
scattering (aerosols plus Rayleigh) and absorption (NO,-,)  to coloration can
be illustrated by rearranging Eq.  (1):
     TOT   dr
                 = b
    scat
        (A)
                            (6)
     Note from Eq.  (4)  that when light absorption  is  negligible  com-
pared with light scattering the clear horizon intensity is  simply:

                              P(A,G)  FS(A)
                                                                    (7)
We now can rewrite Eq.  (6):
dlix]
 dr
                                  I (A)
- 1
                                                                    (8)
     Equation (8) is thus an expression relating the effects  of  light  scat-
tering and light absorption to the change in spectral  light intensity  with
distance along a sight path.  On the right-hand  side of Eq.  (8)  the  first
term is the effect of light scattering (aerosol  plus Rayleigh),  and  the
second term is the effect of light absorption (NOp).  As noted previously,
since b   t and bgbs (due to N02) are strong functions of wavelength and
are larger at the blue end (A = 0.4 ym) of the spectrum than  the red end
(A = 0.7 ym), coloration can result.

     Equation (8) makes clear that NOp always tends  to cause  a decrease  in
light intensity and a yellow-brown coloration by preferentially  absorbing
blue light, whereas particles may cause a blue-white or a yellow-brown
coloration, depending on the value of the quantity  in  the brackets.  If,
at a given point along the sight path, I(A) is greater than the  "clean"
horizon sky intensity Ino(A), then the quantity  in  brackets in the first
term on the right-hand side of Eq. (8) will be negative, which means that
the net effect of scattering will be to remove predominantly  blue light

-------
                                     24
from the line of sight.   This effect would occur when a  bright,  white
cloud or distant snowbank was observed through an aerosol  not containing
N02; scattering would cause a yellow-brown coloration.   If,  however,  I(x)
is less than Ino(A), then the quantity in brackets in Eq.  (8) will  be pos-
itive, which means that the net effect of scattering will  be to  add pre-
dominantly blue light into the line of sight.   This effect would occur when
a distant, dark mountain was observed through  an aerosol  not containing N0n;
scattering would cause the mountain to appear  lighter and  bluish.   Only light
absorption can cause IuU) to be less than Ino(x), and whenever  I(A)  < InoU)>
scattering will add light to the sight path, thereby masking the coloration
caused by NCL light absorption.

     Our visibility models are simply mathematical expressions for the solu-
tion to Eq. (1) for different boundary conditions and for  different values
of bscat' bext' p(0)' and Fs5 as the>y are a"ffectecj b-y natural and man-made
light scatterers and absorbers.  We turn now from this fundamental  viewpoint
to a phenomenological viewpoint, with a summary of the results of an
analysis of visual range in the western United States, before describing the
elements and outputs of the plume and regional visibility models in Chapters
III and IV.

C.   VISIBILITY IMPAIRMENT IN THE WESTERN UNITED STATES

     In support of the development and validation of visibility models, we
analyzed visibility data, including National Weather Service and National
Park Service visibility observations, available nephelometer and telepho-
tometer measurements, and photographs of power plant plumes.  The overall
objectives of the data analysis were:

     >  To determine the magnitude, temporal and spatial
        variations, and natural and source-related causes of
        visibility  impairment  in the western United States.
     >  To identify the meteorological and geographical  con-
        ditions associated with visibility impairment.

-------
                                    25
     Figure 8 shows the locations in the western  United  States  of large
point sources, mandatory federal  Class I areas, and National  Weather
Service (NWS) stations from which meteorological  data  (including  visual
range) were analyzed.   Three-hourly, daytime visual  range  observations
for each of the 18 stations over the period from  1948  to 1976 were analyzed
and were stratified by associated meteorological  conditions — precipitation,
surface wind speed and direction, atmospheric pressure,  relative  humidity,
total sky cover, ceiling height,  season, time of  day,  mixing  depth,  mixed
layer wind speed, and  ventilation—and by year—season,  month,  and time  of
day.  The details and  results of this analysis are presented  in Appendix A.

     Figure 9 displays the frequency distributions of  extinction  coefficients
calculated from visual range observations at 13 NWS stations  in 1976.  Only
observations made on days without precipitation or fog were used  to  compile
these frequency distributions.   Extinction coefficients  were  calculated  from
observed visual ranges using the Koschmieder relationship  [see  Eq.  (5)].

     Several interesting observations can be made on the basis  of Figure 9.
Median visual ranges for nonurban locations are on the order  of 120  km or
greater, corresponding to extinction coefficients less than 0.32  x 10~^  m~  .
At nonurban locations  the visual  range is greater than 100 km nearly three-
fourths of the time, and extinction coefficients  appear  to be asymptotically
approaching a lower bound on the order of 0.2 x 10  m  ,  which corresponds
to a visual range of 196 km, or 122 miles.  The dominant cause  of the
shape of the extinction coefficient frequency distribution in nonurban
areas is the strong dependence of the scattering  coefficient  on relative
humidity.  This effect is due to the hygroscopic  growth  of subm'cron
aerosol particles, thereby adding to aerosol mass, an  effect  discussed
in greater detail in Appendices A and B.

     Figure 10 summarizes the strong dependence of visual  range on relative
humidity at four locations in the Southwest.  The frequency of  occurrence
of visual range greater than the indicated values decreases dramatically
with relative humidity at all locations except Phoenix.   In addition,

-------
                       26
                     i/l    _J

                     S,-'  S  >-
                     OC Z  O  £

                     _g  3  2

                     M o  jZ  S
                     IS) C
                                  5SS  5
                     10 x  ac  i/i a=  o  xqc  13 o
                     < _,  M  M uj  zo«  z on
                             > *t  —• wo a.  •—
                          a    <  t—      h- u-
                          uj  uJt—  h-l*.U-  I-O
                          5  a:   •-* o O  *«
  1.1 *-t ^H CO l/> UJ     UJ tt




  ce » z K *- o     o 1/1
  O >    ^ «C t/> LO fcO l/l Z
  h-    IS) t— >   Z Z   O
    guj l^J t/1 OC H- O O ^~ ^~
    CC I-   UJ Zl-l- Z
    fUJ < UO CO l-l     *-" O
    x i— :E ^ ooo po
    3 to £o a. 
                                                                      I—  '
                                                                      I—l OO LU
                                                                      Z. UJ OH
                                                                      13 O LU
                                                                      a: o
                                                                      LU oo oo
                                                                      I—    -z.
                                                                      00 1— O
                                                                      LU a. H-
                                                                      a:    oo
                                                                      I— LU
                                                                         o oo
                                                                      u_ o; 3
                                                                      o  o. a. S 2

I   	
2  vO ^^cocr»o^c\jn^tf)\or*-co

-------
27
                                                     c; zz
                                                     ^. o
                                                       el
                                                      ! I—

                                                      i Q-
                                                     Q ^3
                                                     UJ O
                                                     00 1C
                                                     oo
                                                     I— 00
                                                     sr >-
                                                     UJ «=c
                                                     KH Q
                                                     O
                                                     1 — I zz.
                                                     u. o
                                                     u.
                                                     UJ (/)
                                                     o 2:
                                                     <_> o
                                                       I — I
                                                     2: t-
                                                     o 
                                                     Q Z r—
                                                        o
                                                     >- •— i S
                                                     O I— HH
                                                     2: <:
                                                     UJ > tD
                                                     Z3 Q; o
                                                     crui u.
                                                     uj oo
                                                     a: CQ o:
                                                     u. o o
                                                     en

                                                     ui
                                                     a;

-------
                              28
!!!«§
9 *"" 5*1®
                 (O
                 C
                 O
                                            •4-J
                                             O
                                             O
                                             1/5
                                                                                                       re
                                                                                                      T3
                                                                                                       ro
                                                                                                       >
                                                                                                       O)
                                                                           to
                                                                           CD
                                                                           QJ
                                                                           I/)
                                                                           re
>-
I—
I—1
O
I—I

rs


LU
                                                                                     O
         •I
         •!
                 O
                 O
8233
"         « in I
                 O
                 re
                 re
,/x
.,-'"'
"x.
•
~x /
§ s s
IPIHH **t MMUMJM4Q IH
^/'/'
^''
1 /
\/' 2 •
S «!•
; ISSSi
/ "i"
i! ;
s s *
*••* |Mf|«
ll^tfl *• «*n»»aj»^

8
*!
•i
s
O
3
                                                                           re
                                                                           c
                                                                           O
                                                                           IM
                                                                                                       
-------
                                     29
the trends in visual  range over three decades--1948 to 1956,  1957 to
1966, and 1967 to 1976--can be determined from Figure 10.   During the
period from 1948 to 1976, the frequency of good visibility decreased
slightly in both Las  Vegas and Prescott, it remained relatively constant
in Farmington, and it improved in Phoenix.  The significant quantities  of
SO  emitted by the copper smelters in Arizona (about 6000  tons  per day  in
  A
1973) appear to be the most significant anthropogenic contributions to
visibility impairment in the Southwest.

     The improvement in visibility in Phoenix during the decade from 1967
to 1976 can be explained by the reduction in emissions (by a factor of
two) that occurred during the period from 1973 to 1976.  As a result of
this pollution control effort, visibility in Phoenix increased  signifi-
cantly from 1973 to 1976, as evidenced by Figure 11.  The  effect of sul-
fate formed in the atmosphere from SO  emissions from the  copper smelters
                                     A^
on visual range in Phoenix is even more clearly indicated  by the increases
in visibility (as shown in Figure 11) that occurred during the  years when
smelter emissions were diminished because of strikes (1949, 1959, and 1967
to 1968).  The effect of total elimination of copper smelter SO  emissions
                                                               A
on visual range is also illustrated in Figure 10, which shows the frequency
distribution of visual range as a function of relative humidity for the
copper strike period, which was July 1967 to March 1968.   Improvements  in
visual range during this-period were observed not only in  Phoenix, but
also in remote nonurban areas, such as Farmington and Prescott.

     The effect of smelter emissions on visual range in remote  nonurban
locations is even more convincingly illustrated by Figure  12, which shows
the frequency of occurrence with which the distant visibility marker (121 km)
was visible in Farmington, New Mexico, stratified by surface wind direction.
Only observations for which relative humidity was less than 60  percent  were
used in this figure so as to minimize the effect that any  dependence of
relative humidity would have on wind direction.   When the  frequencies for
the copper strike period are compared with those for the three  decades, a

-------
                           30
                                                                   > 24 km
                                                                   > 48 km
                                                                    > 64 km
                                                                     97 km
   1950
1955
1960
1965
1970
1975
                               Year
FIGURE 11.   HISTORICAL TRENDS  IN VISIBILITY IN PHOENIX, ARIZONA

-------
      31
               0-  O    Z O>
               fi  LU •— O •—
               O
	  O LU LU <£

00  O CD

VO  OO Z 3 UJ
O1  00

•—  «£
O  £<>H-


S  P2^£
 I   (_> 5*
         O QC
                                                           X

                                                           LU
                                                              fUD


                                                              0>



                                                           < cn
                                                           => f
                                                           00 CT>
                                                           >—I r—
                                                           >
                                                               M

                                                           n: o
                                                           o o
                                                           LU

                                                           D.
                                                 c
                                                 o
                                           LU    U
                                                 •o
                                                 c
a6uey
                                           oo o
                                           •z. uj
                                           o a:
                                           i— 1 1— i

                                           £Q
                                           > o
                                                          oo s
                                                          oa
                                                          O u_
                                                             o

                                                          z z
                                                          CD O
                                                          >- O
                                                          
-------
                                   32
striking improvement in visual  range is apparent,  particularly for the
winds (south-southeast through  west) that would transport smelter emissions
directly toward Farmington (see Figure 8 for the locations of the smelters
and Farmington).  This suggests that the reduced visual  range in Farmington
associated with southwesterly winds is the result of SO   emissions from
                                                      /\
smelters more than 400 km away.  The spatial extent of anthropogenic visi-
bility impairment suggested by these data is also indicated by plume and
regional visibility model calculations presented in the  following chapters.

     Additional conclusions obtained through the analysis of visibility
data from the 18 NWS stations  in the West are summarized below (see
Appendix A for  the details of  this analysis):

     >  Of the  16 NWS stations where long-term visibility
        data appear to be valid (data taken at Alamogordo
        and Ft. Huachuca were  erratic and did not extend over
        the entire 29-year period), visibility decreased at 7
        locations, remained relatively constant at 8, and
        improved at 1 during the period from 1948 through  1970.
        Since 1970 visibility  has  improved  at 12 locations,
        has stayed relatively  constant at 3, and has decreased
        at 1.   Thus, the data  suggest that  pollution control
        during  the 1970s has reversed a downward trend  in  visi-
        bility  that was observed in many western locations during
        the 1950s and 1960s.
     >  Visual  range decreases significantly with increasing
        relative humidity at all 18 NWS stations except Phoenix;
        however, the dependence of visual range on cloud cover is
        less dramatic at most  locations.  The trend of  dependence
        of visual range  on relative humidity agrees with  our  under-
        standing of the  influence  of hygroscopic particle  growth
        with increasing  relative humidity on the light  scattering
        coefficient.

-------
                           33
At most locations reductions in visual  range are corre-
lated with low barometric pressure, which probably
results from the occurrence of high relative humidity
during lows.   However, at Salt Lake City, Ely,  Grand
Junction, and Pueblo, reduced visual range was  corre-
lated with high pressure conditions.  Since high pres-
sure systems sometimes cause air stagnation, the reduced
visual range during highs at Ely and Salt Lake  City
(which are near copper smelters emitting SO ) may be
                                           A
the result of air stagnation.
The stratification of visual range data by ventilation
(the product of mixing depth and average wind speed in
the mixed layer) indicates that reduced visual  range is
correlated with reduced ventilation (stagnation conditions)
in Phoenix, Salt Lake City, Tucson, Billings, Cheyenne, Ely,
Ft. Huachuca, Grand Junction, Great Falls, and  Rock Springs.
Reductions in visual range were found to be correlated with
high ventilation in Denver and Las Vegas, possibly because
urban pollutants were transported into  the sight path between
the city and nearby mountains used as visibility markers.
At 11 of the 18 locations, visual range decreased signifi-
cantly with increasing surface wind speed, suggesting that
windblown dust, particularly at wind speeds greater than
10 m/s,  contributes  to visibility  impairment.  This effect
might explain the decrease in visual range with increasing
ventilation observed in several locations, particularly
Denver,  Las Vegas, Alamogordo, and Winslow.
At most  locations there are no significant seasonal varia-
tions in visual range.  Denver, Las Vegas, and Colorado
Springs  have minimum seasonal average visibilities in the
summer.  At Phoenix, Salt Lake City, Ely, Grand Junction,
and Rock Springs, minimum visibilities occur during the
winter.

-------
                                     34
     >  Variation in visual  range  with  time of day is  negligible
        at most locations.   However,  at some locations,  such  as
        Billings, Cheyenne,  Farmington, Great Falls, and Rock
        Springs, visibilities  at midday (1000 to  1400  hrs)  were
        slightly greater than  at other  times.
     >  Visual  range varies  significantly with wind direction at
        Denver, Las Vegas,  Phoenix,  Colorado Springs,  Farmington,
        Prescott, and Winslow.   This  relationship can  be explained
        by the geographical  locations of emissions sources  relative
        to the sight paths  of  the  NWS observers.   Reductions  in
        visual  range in both Billings and Great Falls, Montana, are
        associated with generally  easterly flow;  the cause  of this
        effect is unknown.   The significant reductions in visual
        range in Prescott,  Hinslow,  and Farmington that are associ-
        ated with winds that transport  smelter S0? emissions  directly
        to the given location  were not  observed during the  copper
        strike period of 1967  to 1968.   During that period, visual
        range increased significantly throughout the Southwest.

To summarize, reduced visual range has  been found to be associated  with:

     >  SO  emissions from copper  smelters
          /\
     >  High relative humidity
     >  Strong winds (windblown dust)
     >  Precipitation
     >  Stagnation conditions  (low ventilation).

-------
                                    35
                 III    THE  ELEMENTS OF  VISIBILITY  MODELS
     This chapter discusses the elements  of visibility modeling that are
common to both the plume and the regional  visibility models.  The specific
models and their outputs are discussed  in Chapter  IV.  Appendices B and C
discuss the modeling of atmospheric  optics and  sulfate formation in greater
detail.  Appendices D and E describe the  plume  visibility model and output;
the regional visibility model  and output  are discussed in Appendices F
and G.

     As shown schematically in Figure 13, modeling of visibility impairment
requires mathematical descriptions for  the following physical and chemical
atmospheric processes in succession:

     >  Emissions.
     >  Atmospheric transport, diffusion, and removal.
     >  Chemical  and physical  reactions and transformations
        of precursors in the atmosphere.
     >  Light scattering and absorption characteristics of
        the resultant aerosol.
     >  Radiative transfer through the  aerosol  along differ-
        ent lines of sight.

     Because visibility models are based  on atmospheric dispersion and
chemistry models, the accuracy of the former depends on that of the latter.
We recognize that future improvements in  modeling dispersion—particularly
on the regional  scale and in complex terrain—as well as improvements in
secondary aerosol formation will  increase the accuracy of visibility models.

A.   POLLUTANT TRANSPORT, DIFFUSION, AND  REMOVAL

     We have developed two visibility models based on two basic types of
dispersion models:

-------An error occurred while trying to OCR this image.

-------
                                   37
     >  A near-source plume model  designed to predict the
        incremental  impact of one  emissions source (such as
        a power plant or smelter)  at distances from 1  to 350 km
        downwind.
     >  A regional model  designed  to predict, over time per-
        iods of several  days, the  impact of several  emissions
        sources within a region with a spatial scale of 1000 km.

     Calculation of near-source visual impacts requires a basic plume model
that accurately predicts the spatial distribution of pollutants and the
chemical conversion of NO to N09 and SO  and NO  to sulfates and  nitrates.
                               £       A       A
The plume model must be  capable of handling the spatial  scale from emis-
sions at the source to at least 100 km downwind.  Because the regional-scale
problem may be caused by long-range transport of pollutants over  a spatial
scale of 1000 km,  an air quality model is needed that can account for mul-
tiple sources and  for temporal variations in mixing heights, dispersion
parameters, emission rates, reaction rates, and wind speed and direction.

     In the following subsections, we discuss atmospheric dispersion  modeling
as it relates to visibility modeling.  In addition, we classify the spatial
scale of the models in further detail:

     >  Initial dilution in a buoyant plume
     >  Gaussian plume diffusion
     >  Limitations on mixing
     >  Plume trajectory box model
     >  Regional transport and diffusion.

1.   Initial Dilution in a Buoyant Plume

     Modeling of the initial dilution of a plume from the top of the  stack
to the point at which final plume  rise is achieved is  important when  model-
ing the conversion of nitric oxide to nitrogen dioxide in a power plant

-------
                                   38
plume because of the quick quenching of the thermal  oxidation  of  NO.   Because
the rate of this reaction is second order with respect  to  NO concentrations,
the rate is fastest in the initial  stages of plume  dilution.   It  is  also
important to account for the initial  dilution of buoyant releases because
the rate of dilution caused by the  turbulent entrainment of ambient  air by
the rising plume parcel  can be considerably greater than that  indicated by
diffusion coefficients based on measurements for nonbuoyant releases (e.g.,
Pasquill-Gifford a , a ).

     Briggs (1969) suggested that the characteristic plume radius increases
linearly with height of the plume above the stack and can  be represented as
follows:

                            Rp = 0.5 (Ah)    .                      (9)

Briggs described the plume rise as  a function of downwind  distance (the  "2/3
power law") as follows:



For initial dilution, we can assume that the plume  is circular in cross
section:
The concentration of a given species at the centerline of the plume can be
calculated by a modified Gaussian model that can be represented as:
where V is the velocity of the parcel, which has a horizontal component
(the wind speed u) and a vertical component w, which can be calculated
by differentiating Eq. (10) as follows:

-------
                                    39
With this formulation, time-dependent plume temperature and NO concentra-
tions can be calculated for accurate prediction of the thermal oxidation
of NO during plume rise.

2.   Gaussian Plume Diffusion

     After the plume has achieved its final height (about 1  km downwind),
plume concentrations for uniform wind fields can be adequately predicted
using a Gaussian model if the wind speed u at plume elevation H (h  + Ah)
and the rate of diffusion are known for the particular situation so that
dispersion coefficients (o ,o )  can be selected:
Equation (14) is appropriate for a conservative species and can be modi-
fied to be appropriate for a nonconservative species by changing the
source term Q.

     It is necessary for calculating plume visual  impact to.integrate,
along the line of sight, the primary and secondary particulate and nitro-
gen dioxide concentrations.  Equation (14) can be  integrated (Ensor, Sparks,
and Pilat, 1973) in the cross-wind direction y from y = -°° to y = +°° to
obtain the optical  thickness of the plume:

-------
                                    40
            TPy
+ exp - ±
                                                                     (15)
where Q1 is the integral of the flux of plume extinction coefficient over
the entire plume cross section at downwind distance x.   In the vertical
direction z, from z = 0 to z = +°°, the optical  thickness is:
3.   Observer-Plume Orientation

     The magnitude of the visual impact of a plume depends on the orien-
tation of the observer with respect to the plume because the plume optical
thickness will vary depending on this orientation.  Figure 14 shows plan
and elevation views of an observer and a plume and indicates that the sight
path distance through the constituents of the plume is a function of angles
a and e.  The optical thickness at any angle a and any angle 3 can be deter-
mined as follows:
Figure 14 suggests that plume optical thickness is greater for horizontal
sight paths than vertical ones, particularly during stable conditions when
the plume cross section is flattened.

-------
                             41
                   (a)  Plan View
%%^^//^^^^
                (b)  Elevation View
Source:  Latimer and Samuelsen (1978),
FIGURE 14.    GAUSSIAN PLUME VISUAL IMPACT MODEL:
             OBSERVER-PLUME GEOMETRY

-------
                                   42
4.   Limited Mixing

     When vertical  diffusion is  limited  by  a  stable capping layer, Eq. (14)
is no longer valid, and a Gaussian  formulation with terms for reflection
from the top of the mixed layer  (at altitude  H  )  is more appropriate.  In
this instance of limited mixing, the plume  concentration becomes uniformly
mixed in the vertical  direction  for 0 < z  <  H  and:
                                      ~   —  m
TT
 '
                                       • s (tfl
The calculation of plume optical  thickness  in  the y-direction becomes simply:
Equation (19) suggests a simple box  model  for calculating  the reduction  in
visual range of a plume after it has become  uniformly  diffused  in  the ver-
tical direction, which we discuss in the following  subsection.

5.   Plume Trajectory Box Model

     The reduction in visual  range resulting from a plume  that  is  uniformly
mixed in the vertical direction can  be evaluated simply, as  Figure 15
illustrates.  Latimer and Samuelsen  (1970) showed that reduced  visual range
resulting from pollutants in  a plume is given by:
            r  =
             v   bext-0
[3.912  - tofyf} - J     .                 (20)
When plume material does not significantly affect the intensity  of the
horizon sky, the second term in the brackets drops out.   After noting that
the background visual range (without the plume)  is:

-------
43
                                 Q
                                 O
                                 X
                                 O
                                 CO
                                 o

                                 o
                                 Ul
                                 '-3
                                 LT>
                                 ex.

                                 C3

-------
                                    44
                                   3 912
                                =
we can rearrange Eq. (20) as follows:
                          rv= rvo(] -1*7)    '                   (22)

The fractional reduction in visual  range then becomes:


                                       Q'(x)
                                     3.912 uH

where Q' is the integral of the flux of the plume extinction coefficient
over the total plume cross section at downwind distance x.

     To illustrate the use of Eq. (23), we evaluated the percentage reduc-
tion in visual range resulting from three S02 emissions sources, assuming
average afternoon ventilation for Winslow, Arizona (u = 6.7 m/s, Hm = 2613 m),
a sulfate formation rate of 0.5 percent per hour, and a b___^-to-mass ratio
          1     3
of 0.04 m  /yg/m  of S0| and persistent meteorological conditions.  Three
S02 emissions  rates were selected:  2000 tons per day  (representative of
a large copper smelter  complex), 200 tons per day (representative of a
large coal-fired power  plant without S02 scrubbers), and 20 tons per day
(representative of a large coal-fired power plant with 90 percent S02
control).  The results  of this calculation using this  simple model are
shown in Table 2.

-------
                                    45
                TABLE 2.   PERCENT REDUCTION IN VISUAL RANGE BY
                          THREE LEVELS OF S02 EMISSIONS
Downwind
Distance
(km)
50
100
200
500
1000
2000
Tons/Day
1.9%
3.8
7.5
18.1
34.5
200
Tons/Day
0.2%
0.4
0.8
1.8
3.5
20
Tons/ Day
0.0%
0.0
0.1
0.2
0.3
     As the sample calculations summarized in Table 2 illustrate, the most
significant reduction in visual range from anthropogenic omissions may not
occur close to the source, but rather, at locations hundreds of kilometers
downwind from the source.   However, the values in Table 2 are examples for
average conditions and an  assumed sulfate formation rate.  Equation (23)
makes clear that visibility impairment is a function of the ventilation and
the total quantity of light scatterers and absorbers in the plume.  It should
be noted that these calculations ignore the effect of SO,, and sulfate removal
processes that decrease the sulfate concentrations and thereby reduce visi-
bility  impairment.  (Such processes are considered in the plume and regional
visibility models.)  As demonstrated by these simple calculations, secondary
aerosol formation has a significant effect on the magnitude of impairment
for given emission and meteorological conditions.  Equation (23)  is a simple
calculation through which a first-order estimate of an emission source's
impact  on visual range can be made.

-------
                                   46
6.   Regional Transport and Diffusion

     The modeling of visibility impairment on a  regional  scale  requires  the
use of a model that accounts for time-dependent  meteorological  conditions,
multisource emissions, and pollutant removal  through surface deposition,
washout, rainout, and the like.  We selected  the SAI Northern Great  Plains
grid model (Liu and Durran, 1977) as the basis for our regional  visibility
model.  Appendix F describes the model  in detail.

     The model is composed of two interconnected submodels:   a  mixed layer
model and a surface layer model.  The mixed layer model  treats  transport and
diffusion above the surface.  A grid approach is adopted to  facilitate the
handling of multiple sources and complex chemistry.   The major  feature of
this model is the assumption that pollutant distribution is  nearly uniform
in the vertical direction.  With this assumption, a simplified  form  of the
general atmospheric diffusion equation can be invoked.

     The surface layer model calculates the pollutant fluxes lost to the
ground.  The surface layer, a shallow layer immediately above the terrain,
is embedded within the mixing layer.  If pollutants originate from either
elevated sources or distant ground-level sources, most of the pollutant  mass
is contained in a layer aloft, i.e., in the mixed layer.  The removal  pro-
cesses consist of the diffusion of the pollutants through the surface layer
to the ground, followed by absorption or adsorption at the atmosphere-ground
interface.  A unique feature of the surface layer is its diurnal variation
in surface temperature, which is a result of daytime heating and nighttime
cooling.  This variation affects the vertical pollutant distribution through
atmospheric  stabilities, and, consequently, the rate of surface uptake of
pollutants.

     The  regional model assumes  vertical homogeneity  in the concentration
distribution.  One of the reasons for this assumption is that the vertical
diffusion term, based on dimensional analysis, is about 100 times greater

-------
                                   47
than the transport term, and the horizontal diffusion term is only a frac-
tion of the transport term.

     Assuming that the concentration distribution in the vertical is nearly
uniform below the base of the temperature inversion, a vertically averaged
concentration of species i may be computed from the following equation:
  3C".     ZC*     3 C",
                  3
                        - (Cj - c0.)-D.c(D)    ,    1-1. 2,..., N    ,   (24)

 where
           CQ.  = the background concentration of species i,
          IT,  v  = the vertically averaged horizontal  wind
                 components  ("u *jf  u dz/H, v =/Q v dz/H),
             D  = the two-dimensional  divergence [D = (3i7/ax)
                 + (9v/3y)],
          ?(D)  = a step function defined by

                                   n    for    D >  0
                            c(D) =                                        (25)
                                   ' 0    for    D £ 0    ,
         S^ R.  = rate of change of concentration of species i due
                 to emission sources and chemical reaction.

In the derivation of Eq. (24), the following assumptions were made:

     >  Deviations from the average  concentration, c~. ,  in the
        vertical direction are small.
     >  The vertical velocity at the top boundary is approxi-
        mately given by:

-------
                                    48
                                                                  (26>
     >  The diffusive  flux of  pollutants at the top boundary is
        negligible.
     >  The following  relationships  hold for the reaction and
        source/sink  terms:

                    R-- (c, ,C£ t - • • »c,.)  =  R. ic-j »Cp > « • • »c., )            (27)


                              S.(c.)  -  S.^)    .                 (28)

B.    ATMOSPHERIC CHEMISTRY

     The visibility models  require calculations of the conversion of pre-
cursors to species that cause visual  effects,  namely,  nitrogen dioxide  and
secondary aerosol (sulfate,  nitrate, organics).

1 .    Conversion of NO to NOp
     As previously noted, nitrogen dioxide gas causes a yellow-brown dis-
coloration of the atmosphere.  Although some discoloration can be caused
by wavelength-dependent light scattering by submicron aerosol, we demon-
strate in Chapter IV that the dominant colorant of power plant plumes is
N02 and that yellow-brown discoloration may be apparent at significant
distances downwind of large coal-fired power plants, particularly in areas
where the background visual range is excellent.

     Very little N02 is emitted directly from power plants.  However, color-
less nitric oxide is formed by the thermal oxidation of atmospheric nitrogen
at the high temperatures experienced in the combustion zone (the boiler in a
power plant) and the oxidation of nitrogen that may be present in the fuel.
Chemical reactions in the atmosphere can form sufficient NOn from NO to cause

-------
                                    49
atmospheric discoloration.  Available measurements of NO and NCL concen-
trations in power plant plumes in nonurban areas suggest that the conver-
sion of NO to NOp can be calculated from a simple set of three reactions.

     The first of these is the thermal oxidation of NO to N02:

                           2NO + 02 •* 2N02    .                      (29)

The reaction is termolecular but bimolecular with respect to NO; it  is
therefore very fast at high concentrations of NO but slow at the lower  con-
centrations that exist in the atmosphere or in a plume.   The reaction rate
for Eq. (29) [based on Baulch, Drysdale, and Home (1973)] is:
     d[N02]
       dt
x 10"12 exp(1^6fl[NO]2[02] ppm/s    .          (30)
     The reaction with ozone also affects the conversion  of NO  to  NO,,:

                           NO + 03 -* N02 + 02                       (31)

The reaction is fast,with a rate (Leighton, 1961;  Davis,  Smith, and
Klauber, 1974; Niki, 1974) at 25°C of:

                   d[NO?]
                   —g^- = 0.44 [N0][03] ppm/s     .                 (32)

This reaction accounts for the ozone depletion measured within  power plant
plumes and is important because ozone concentrations  can  be high even in
nonurban regions.  Measured ozone concentrations  in nonurban areas of the
western United States range from 0.02 to 0.04 ppm.

     Whereas the thermal  oxidation rate  [Reaction (30)]  decreases as the
plume mixes (because the  NO concentration decreases),  the formation  of

-------
                                  50
nitrogen dioxide via Reaction (31)  is enhanced as  the plume mixes,  because
additional ozone from the atmosphere is mixed into the plume,  allowing
Reaction (31) to proceed.  When there are no reactions converting  N02 to
NO (e.g., at night), Reaction (31)  proceeds until  all  of the NO in the  plume
is converted to N02 or until  the ozone concentration in the plume  drops to
zero.  Therefore, the rate of conversion of NO to  NOp via Reaction (31) is
limited by the rate of plume mixing that provides  the necessary atmospheric
ozone.

     To complete the set of chemical reaction mechanisms, we must  consider
the photodissociation of NOp.  When sunlight illuminates a plume containing
nitrogen dioxide, short wavelength  light and ultraviolet radiation are
absorbed by the NO,,.  As noted above, absorption of the shorter wavelength
light produces the characteristic yellow-brown color associated with N02-
Absorption of the more energetic ultraviolet light (x < 0.4 pm) results in
dissociation of the N02 molecule:

                         N02 + hv -*• NO + 0    .                      (33)

                           0 + 02 + 03    .                         (34)

Leighton  (1961) gave the rate of Reaction (34) as:
                                   [N0] ppm/s    ,                  (35)
where K. depends on the amount of light incident on the nitrogen dioxide.
Davis, Smith, and Klauber (1974) gave the following expression for K, as
a function of the solar zenith angle X:

                     K. = 1 x 10~2 exp(- 7^|) s"1    .             (36)
                                       \        /

     With this set of chemical reactions, the chemical conversion of NO to
N02 in the atmosphere can be calculated from background pollutant concen-
trations and from plume NOV increments using the technique suggested by

-------
                                   51
Latimer and Samuelsen (1975) and White (1977).   Making the steady-state
approximation, we have:
                                  K
                          [N02] = / [N0][03]    ,                   (37)

where
                          [NO] = [NO ] - [NOJ                      (38)
                                    A       C.

and

               [03] = [03]b - ([N02] - [N02]t  - [N02]b)    .          (39)

Substituting Eqs.  (38)  and (39)  into Eq.  (37)  we can solve for the  concen-
tration of N00:
        [N02] =0.5
[NOX] + [03]b + [N02]t
                                                       K
                                                        r
                                                                   2
                                        1/2
                                                                !
                                                                J
                                                                    (40)
     Using this formulation to compute NO to N02  conversion  in  a  hypothetical
power plant plume, Latimer and Samuelsen (197G) studied  the  sensitivity of
N02 formation to the rate of plume dilution, background  ozone concentration,
and solar radiation.  The results of this analysis  are presented  in  Figure 16.
This figure shows that thermal  oxidation (e.g., [03]  = 0)  converts up  to 10
percent of the plume NO to N02> and additional conversion  results when ambient
ozone is mixed into the plume.   A recent comparison of observations  with cal-
culations using Eq. (40) indicates good agreement,  particularly if the

-------
                                     52
*  *   "2
8n  ^    •«
                                                                                         Cb
    OJ
    •4-'
    ro    ^~^»
    O    CO
          r-.
    >>    CD
J   +>    '-
                                                                                                c
                                                                                                a)
                                                                                                t/i

                                                                                               'a!
                                                                                               oo
                                                                                                (O
                                                                                                S-
                                                                                                O)
                                                                                         (O    'I-
                                                                                         I  i     1 _\


                                                                                         co     (O
           OJ
           o

           13
           O
           co
                                                                                                      U.
                                                                                                      O
                                                                                                      •a:
                                                                                                      a:
                                                                                                      :r
                                                                                                      h-
                                                                                                      O  O
                                                                                                      ^;g
                                                                                                      ii 11—«
                                                                                                      z:  o

                                                                                                      a.
                                                                                                          o:
                                                                                                       cr
                                                                                                       UJ
                                                                                                       a.
                  O t—
                  i—i 2:
                  CO LU
                  C£ O
                  LU z
                  > o

                  g°
                  o uj

                   CsO
                  o rvi
                  z o

                  o o
                                                                                                       o o
                                                                                                       z a:
                                                                                                          CQ
                  t-H O
                                                                                                       CO
                                                                                                       UJ i— i
                                                                                                       co o
                                                                                                       CD

-------
                                     53
diffusion of the plume is correctly calculated by using fitted dispersion
coefficients based on plume diffusion measurements (see Figure 17).

2.   Conversion of Gases to Particles

     Although SOp, NO, and N02 gas do not scatter liqht appreciably,  they
react in the atmosphere to form secondary sulfate and nitrate particles  in
the size range that is most effective at light scattering (0.1  to  1.0 ;im).
In many situations, sulfate and nitrate are the dominant contributors to the
scattering coefficient of the atmospheric aerosol.  It is essential,  there-
fore, that the effect of these secondary aerosols and the rate at  which  they
are formed from precursors be included in visibility models.

     During this first year of development work, we have concentrated on
developing the atmospheric optics and visibility impairment components of
the plume and regional visibility models.  The development of a model to
predict the rate of formation of sulfate and nitrate aerosol  based on the
fundamental chemical reactions and physical processes would be a tremendou:.
undertaking.  Furthermore, even if such a model were available, we do not
know the background atmospheric concentrations of the species responsible
for the conversion of gases to particles.

     We have therefore adopted the approach of calculating gas-to-particle
conversion using measured rates of reaction appropriate for the clean
(Class I) areas of the country.  We recommend, however, that consideration
be given in future visibility model development work to the incorporation of
fundamental gas-to-particle reaction mechanisms in the visibility  models.

     The measured rates of conversion of the gaseous species to particles
vary over several orders of magnitude, depending on the amount of  sunlight,
the concentrations of hydrocarbons, ammonia, manganese, iron, and  other
chemical species, and the relative humidity.  Available data suggest  that

-------
54

-------
                                     55
the rate of conversion of SCL to sulfate particles is much greater in
polluted urban atmospheres and in locations where relative humidity is
high.  Appendix C summarizes the fundamental reaction mechanisms and
the available measurements of the rate of sulfate formation in the
atmosphere.  Other recent reviews of sulfate formation include those
of Calvert et al.  (1977), ER&T (1977), and Levy, Drewes,  and Hales (1976).
Orel and Seinfeld (1977) have reviewed nitrate as well as sulfate informa-
tion, particularly in polluted urban atmospheres.  For our initial visi-
bility model development work, we have modeled gas-to-particle conversion
using pseudo-first-order rate constants typical of clean  areas.   Levy,
Drewes, and Hales (1976), in their review of SOp oxidation in plumes, sup-
ported such an approach.
     We calculate the conversion of S00 and NO  to sulfate and nitrate as
                                      2       x
follows:
                          9[S02]
                          ~
                          3[NOl
                                               .                     (42)
The integral of the flux sulfate and nitrate mass contributed by a  given
emissions source (Qso?' QNOX) over the entire plume cross section at a  given
downwind distance or transit time (t = x/u)  can be calculated as follows:
                               Qso2 1  - e         •                  (43)

where r^  and r2 are simply the ratios of molecular weights  of sulfate  to  S02
(r, = 1.5) and nitrate to N02 (r2 = 1.35).   The mass  of the ammonium ion
(or other cation) and water associated with the sulfate and nitrate also
contributes to the total  aerosol  mass concentration.

-------
                                   56
     The effect of plume dilution on gas-to-particle conversion  can  vary
depending on the relative contribution of reactions with plume constituents
(e.g., catalytic oxidation of S0? on particle surfaces  or in  the liquid
phase by metal ions) and reactions with trace species in the  background
atmosphere (e.g., the reaction of S02 and NOX with OH',  HOA, HpO, NhL,  and
RO^).  For heterogeneous catalytic reactions on emitted primary  particles,
the rate of aerosol formation decreases with plume dilution.   For example,
the fractional rate of S02 conversion to sulfate becomes:
                      i    3[SO?]
                               -" CCatalyst3    '                  (45)
                       2-

The concentration C of conservative plume species (e.n., precursor SOX and
NO  or primary particulate) decreases with time after emission and can be
described mathematically (Schwartz and Newman, 1978) as:

                               C « t~n    .                          (46)

Thus, if heterogeneous reactions with primary particles are the sole con-
tributors to secondary aerosol, one would expect a secondary aerosol forma-
tion rate that rapidly decreases with time after emission from the stack;
for example,
                               afSO^l
                                                                    (47)
                                 at

     Furthermore, if a catalyst were used up, this reaction would decrease
even more rapidly and would eventually be quenched.  However, the formation
rate of secondary aerosol by reactions with trace constituents of the back-
ground atmosphere (such as OH*, HOA, MHo) or background aerosol increase with
increasing plume dilution and will dominate at long reaction times.  This
occurs because, with increased mixing associated with plume dilution, fresh
ambient air (containing the reactive species) is mixed into the plume.  With-
out plume dilution, the reactive species are used up and no further conversion
takes place.  The process becomes diffusion-limited in the same way N02 pro-
duction in a plume is limited by the rate at which ambient ozone is mixed into
the plume.

-------
                                   57
     At this stage in visibility modeling,  we are using pseudo-first-order
rate constants to model  the conversion of S00 and NO  to sulfates  and
                                            2       x
nitrates.   In our sensitivity analyses, described in Chapter  IV, we  selected
sulfate formation rates  ranging between 0.3 and  1  percent per hour and, due
to the lack of quantitative data due,  in part, to the uncertainty  in measured
nitrate concentrations (Spicer and Schumacher, 1977), a nitrate formation
rate of zero.
C.   AEROSOL SIZE DISTRIBUTION

     To determine the visual  effects of aerosols,  one must specify or cal-
culate aerosol physical size  and composition.   This section reviews the
available data on atmospheric aerosol  size distributions,  particularly the
recent work of Whitby and his coworkers.   We then  discuss  the types of
aerosols that are important for visibility considerations—background,
primary, and secondary aerosols--and how they are  currently treated in
the visibility models.

     Atmospheric aerosols can be grouped into a trimodal  size distribution.
Figure 18 shows the three modes (nuclei,  accumulation, and coarse particles)
and the processes that form them.   According to Whitby and Sverdrup (1978):

          The physical separation  of the fine and  coarse modes
          originates because  condensation produces fine parti-
          cles while mechanical processes produce  mostly  coarse
          particles.  The dynamics of fine particle growth
          ordinarily operate  to prevent the fine particles from
          growing larger than about 1  ym.  Thus as a first
          approximation, the  fine  and coarse modes originate
          separately, are transformed separately,  are removed
          separately, and are usually chemically different.

     Figure 19 shows the various ways of plotting  size distribution infor-
mation.  Figure 19(a), a number size distribution, is the  plot that Junge
(1963) originally used for his data.  This plot led to the aerosol power
law formulation:

-------
                               58
                         CHEMICAL CONVERSION
                           OF GASES TO LOW
                          VOLATILITY VAPORS
 0.002
                         CONDENSATION GROWTH
                            OF NUCLEI
                                                 WINDBLOWN DUST
                                                      +
                                                   EMISSIONS
                                                      +
                                                   SEA SPRAY
                                                      +
                                                   VOLCANOES
                                                      +
                                                 PLANT PARTICLES
           0.01
           1    2
  Particle Diameter (pm)
                                                     10
                                                                    100
   TRANSIENT NUCLEI OR
   AITKEN NUCLEI RANGE
ACCUMULATION
   RANGE
                 FINE PARTICLES
 MECHANICALLY GENERATED
~   AEROSOL RANGE
                                                  COARSE PARTICLES
Source:   Whitby and  Sverdrup  (1978).
FIGURE 18.   SCHEMATIC OF AN ATMOSPHERIC  AEROSOL SURFACE  AREA
              DISTRIBUTION SHOWING THE PRINCIPAL MODES,  SOURCES
              OF MASS FOR  EACH  MODE,  PROCESSES  INVOLVED  IN
              INSERTING MASS IN EACH  MODE, AND  REMOVAL MECHANISMS

-------
                   59
ro
 I
 C)
 o
JO6



I05



I04



I03



I02



10'
      ID'1



     JO'2



     IO'3
     ID-
              d log Dp
                        r*«0.99
        0.001 0.01    O.I
                      1.0
10   100
                       D  (UN)
    (a)  Power Function Fitted to the Number
         Distribution over the Size Range
         0 to 32 pm
FIGURE 19.   AVERAGE URBAN MODEL AEROSOL DISTRIBUTION
            PLOTTED IN FIVE DIFFERENT WAYS

-------
                                             60
> N

0) c/i

rO C
-P (O
0)
Q.
999

  99

  90

  70
  50
  30

  10
    I

  0.1
               06VT «1.62/1
               
-------
                                     61
                           d log D  " cDp     '                     (48)

where N  is the number of particles of diameter Dp.  Figure 19(b) shows the
standard lognormal plot.  Figures 19(c), 19(d), and 19(e) show the number,
surface  area, and volume distributions of an urban aerosol.  These last
three plots show the three distinct aerosol modes:  nuclei (0.001 to 0.1 ym),
accumulation  (0.1 to 1.0 ym), and coarse (>1 ym).

     Whitby and Sverdrup (1978) recently computed a table showing typical
aerosol  size distributions and concentrations based on measurements in many
locations.  Table 3 summarizes the mass median diameters (DG), the geometric
                                                               3   3
standard deviations (o), and the volume concentration (V in ym /cm ,  which
                                          3                            3
is equal to the mass concentration in yg/m , divided by density in g/cm )  of
each of  the modes for eight classifications of aerosol.  Table 3 shows only
a  small variability in the accumulation and coarse mode size distributions
for the  variety of aerosol types measured (excluding the marine aerosol).
The average specifications for the accumulation mode and the coarse distri-
butions are summarized below:

                    Mode               DG              °q
                Accumulation     0.29 ± 0.06 ym     2.0 ± 0.1
                Coarse           6.3  ± 2.3  ym     2.3 ± 0.2

The data suggest that the average specifications (mass median diameter and
standard deviation)  of the accumulation and coarse modes fit a wide range
of atmospheric conditions, a finding that greatly simplifies the calculation
of the scattering properties of the atmosphere.

     Figure 20 shows the results of our calculations of the scattering
coefficient-to-volume ratio for a variety of different aerosol size distri-
butions.  The calculations are based on Mie theory.  The average specifica-
tions and corresponding scattering properties of the accumulation and  coarse
modes are also given in Figure 20.   As this figure shows, the accumulation
mode aerosol  is roughly an order of magnitude more effective per unit  volume
than the coarse mode aerosol.

-------
62















o
co
o
o;
ill
LLJ

o


CO
£
> ^ °.
CO CM

^


C7 P*^
o
CM

-H o
CJ3 E 1
Q 3. CM
* 1 •""

^««

(U
T3
g

C
0
•f-
ro
^—
3
3
U
U
**




OO
6 o
E 0
a
x_^


^0
CM*


,-j
o E| ro
Q 3.
^J o
1
! _





Qi
•o
O
£
•r—
"o
3
zn






co
E in
o o
=• --i o
co o
E
3. 0

Hvo
-



1 O^
—J •—
0 C] 0

-fj 0*





r^
O
VI
0 oj
s- o
a> re




«*
fv^
CM


CM
r—
•
CM

Uf)
•
•*




O
•
**t"



cS


vo
CO
•
o




Q}
CM
O
•
0

r—



CO
CM
O

O




•o

CO


CM
O
•
CM

«3
•
Lf>




CM
O
CO




CM


Lf)
CM
•
O





CM
10
»
O

•
r—*



r-.
CM
O

O








•a
C V)
to o
t)
"O >-
C 3
3 O
0,0
CHr—
J^ (O
o o
to o
CQ i—


CO
o
CO


r_
CM
•
CM

r-.
•
UO




«3-
CO
co



CM


CM
CO
•
0





CO
10

o

CO



CO
CO
0

0









(U
en
fO
S-
0)



O
^T
CM



IT)
•
CM

LO
•
LT>




O
CM
r—



CTi
•


00
r—
•
o






r—
•
o

•
p—



IT)
i—
o

o



H^
vo
f*s.
CM
^—

(U
E
3
r>_
Q.


>v-


* •+-










































co"
f^
r—
v_
00
T3
C
re

_>>
+->

.c


(U
S
3
o
CO

-------
63
                             CJ
                             Q
                                     CO
                                     t—t
                                     o:

                                     co
                                     »—i
                                     a

                                     LU
                                     M

                                     to

                                     OO
                                     Z3
                                     O
                                     t-H
                                     a:
                                     
-------
                                    64
     If the scattering coefficient  corresponding  to each of the modes for
the different aerosols sampled by Whitby and Sverdrup  (see Table  3)  is  cal-
culated, the accumulation mode is the dominant scattering mode, with the
coarse mode contributing a small  amount and the nuclei  mode a  negligible
amount.  For the clean continental  background aerosol  (second  entry  in  Table
3), we calculated that the total  scattering coefficient (b    ,) equaled
         _4  _i                                           scat
0.23 x 10   m  , which is very close to the minimum scattering coefficient sug-
gested by the data shown in Figure  9 (Chapter II).  The accumulation mode
contributes 0.09 x 10   m   (39 percent of bc^a.), the  coarse  mode 0.04 x
   A   1                                    scat                   .   -1
10   m   (17 percent of b$cat), and Rayleigh scattering 0.10 x 10   m  (43
percent of bsca+)-  In the clean  background case, the  contribution of the
accumulation mode to the extra extinction (b  ) above  Rayleinh was 69 per-
cent of the total.  This clean background aerosol corresponds  to  a visual
range of 170 km, or 105 miles (3.912/b   .).  For the  average  background
                                                          "    _A   -i
aerosol (third entry in Table 3)  the computed b    is  0.57 x  10" rrf ,
                                               scan
corresponding to a visual range of  69 km.  In this case, the accumulation
                           4  -1
mode contributed 0.27 x 10"  m   (46 percent of b   ,), the coarse mode
          4   i                                   scat          4    i
0.21 x 10   m   (36 percent of bscat)» and Rayleigh 0.10 x  10   m   (17 per-
cent of b,.,.).   These calculations indicate that for  background  conditions
         scat
the accumulation mode is a larger contributor to light scattering than  the
coarse mode but that the coarse mode is a nonnegligible component of the
scattering coefficient of the background atmosphere.   This  situation strik-
ingly contrasts with that of polluted urban atmospheres, in which the
accumulation mode causes more than  90 percent of the total  scattering coef-
ficient.  We should also note that  the average background presented  in
Table 3 is not as clean as the average background in the nonurban western
United States, as Figure 9 suggests.

     In our visibility models, we have used the size distributions  given  in
Table 3 for specifying ambient background (second and  third  items in Table  3)
and plume aerosol (eighth item).   We then calculated optical  properties of
the aerosol (using Mie theory) from the computed concentrations of coarse and
accumulation mode (sulfate, nitrate, and associated cations  and water)
aerosol.

-------
                                   65
D.   ATMOSPHERIC OPTICS

     In the atmospheric optics component of the visibility models,  the
light scattering and absorption properties of the aerosol  and the resultant
light intensity for various illumination and viewing situations are computed.
The details of these calculations are given in Appendix B; the major points
are summarized in this section to give the reader an overall  view of the
process.

1.   Calculation of the Scattering and Absorption Properties

     After the concentrations of the pollutants are specified by the trans-
port and chemistry subroutines, their radiative properties must be  deter-
mined.   For N02, the absorption at a particular wavelength is a tabulated
function (Nixon, 1940) multiplied by the concentration.  For  aerosols, the
procedure is more complicated, however.

     In general, a particle's ability to scatter and absorb radiation at
a particular frequency is a function of size, composition, shape, and
relative humidity.  Because we wanted to be able to alter  the size  distri-
bution  of both primary and secondary particles, we needed  to  be able to
compute the effect of particle size on the wavelength dependence of the
extinction coefficient and the scattering distribution function.   The only
rational method of making this computation is to use the solution of
Maxwell's equations for scattering by a sphere, the so-called Mie equations.
To verify that these calculations were appropriate for atmospheric  aerosols,
we compared them with the empirical correlations of scattering to mass and
found substantial agreement, as discussed below.

     The calculations were performed using an IBM subroutine  written by
J. V.  Dave (Dave, 1970).   The required inputs are the particle size param-
eter (ratio of the circumference to the wavelength of radiation), the index

-------
                                   66
of refraction (real  and imaginary part),  and the number and  location  of the
scattering angles (between 0° and 180°).   The output is the  scattering  and
absorption cross sections and the Stokes  transformation matrix  (Van De  Hulst,
1957), which can be  simply converted to the scattering distribution assuming
randomly polarized light.  The scattering and absorption properties per par-
ticle are then summed over the particular size distribution  in  such a way
that as the size distribution changes so  do the radiative properties.

     Different types of empirical correlations have been made in  recent years
relating particle scattering properties to particle mass.  The  property mea-
sured has been either the volumetric scattering coefficient, as measured by
an integrating nephelometer, or the extinction coefficient,  calculated  from
the observed visual  range.  Among recent discoveries is the  conclusion  that
the scattering properties of urban atmospheres correlate much better  with
the submicron accumulation mode concentration than with total mass.   A
second important development is that for most of the United  States and
Europe, sulfates are generally a significant fraction of submicron accumu-
lation mode mass.

     Many studies of the empirical correlations of scattering coefficients
to sulfate mass have been performed.  Table 4 summarizes some of  these
measurements.   Similar tables have appeared  in other reports, such as that
by Trijonis  and Yuan (1977).  The correlation coefficients for these rela-
tionships have  been very  high (0.7 to 0.9),  supporting the dominant role of
sulfate  in scattering.  Of  particular importance is the use, by many
researchers, of visual range data (e.g., airport visibility) derived from
actual,  though  somewhat  imprecise, visual perception of objects in the atmo-
sphere.  Thus,  it appears that sulfates play an important role in visibility
impairment.

     Calculations of scattering-to-volume ratios (see Figure 20)  reveal that
the maximum theoretically possible value is about 0.06, as expressed  in the

-------
                                     67
          TABLE  4.   ESTIMATES OF EXTINCTION COEFFICIENTS PER UNIT MASS
                                                          Extinction
                                                         Coefficients

                                                      COO4 m~V(Mg/m3)]
Source
Regression models
(Trijonis and Yuan, 1978)










Regression models
(Trijonis and Yuan, 1977)


Dust storms
(Hagen and Woodruff, 1973)
Regression model
(White and Roberts, 1975)
Regression model
(Cass, 1976)
Calculations for a model aero-
Location
Chicago
Newark

Cleveland

Lexington

Charlotte

Columbus

Salt Lake City
Phoenix
(county data)
Phoenix
(NASN data)
Great Plains

Los Angeles
Los Angeles
0
Sulfates
0.04
0.03*
(0.02)
0.06*
0.08
0.07*
0.06
0.06*
0.11
0.11*
0.12
0.13*
0.04
0.04*
0.04
0.03
NC

0.07
0.16
0.09*
.05-0.10
Nitrates
(0.00)
(0.00*)
(0.00)
(0.00*)
(0.00)
(0.00*)
(0.00)
(0.04*)
(0.00)
(0.00*)
0.09
(0.06*)
0.13
0.10*
0.05
0.03
NC

0.05
(0.00)
0.05*
NC
Remainder
of TSP
(0.000)
(0.000*)
0.026
0.014*
(0.000)
(0.000*)
(0.000)
0.019*
(0.001)
(0.000*)
(0.000)
(0.001*)
0.004
0.004*
(0.000)
(0.000)
0.001

0.015
0.008
(0.004*)
NC
sol of (NHjpSOjj at 70% RH
(Waggoner fit al., 1976)

Regression model
(Waggoner et al., 1976)
Southern Sweden  0.05
NC
( ) = not significant at the  95  percent confidence level.
NC  = not calculated.
*Based on nonlinear RH regression model, with  insertion of average RH.
Source:  Trijonis and Yuan  (1978).

-------
                                  68
                      *
units used in Table 4.    However,  the reported empirically  determined
values range from about 0.03 to 0.1.   This discrepancy  was  resolved  by
including the mass of liquid water associated with the  sulfate.   Investi-
gators have found better correlations with scattering-to-mass  ratios that
depend on relative humidity.  These fits are of the form:
                                                                    (49)
                                    1 - RH
where c represents the scattering-to-mass ratio at 0 percent relative
humidity.  The range of these values is between 0.02 and 0.04,  which  is
in agreement with theoretical values shown in  Figure 20."*"

     To account for the effects of relative humidity, we simply added  the
amount of water absorbed by the sulfate particles:
                            MaSSSulfate + MassCation + MassWater
Then we used a formula from Winkler (1973)  to account for the mass of water
as a function of relative humidity.  Finally, we compared the dependence of
the scattering-to-mass ratio on relative humidity determined by Cass and
Trijonis with calculations using the following assumptions:
  This was computed from the maximum value of 0.08 x 10"^ m~'/ym3/cm3 in
  Figure 20 assuming the sulfate was associated with ammonium ion as
  (NH4)2S04:
                                           cm3               132
W
A
                                     l .8 g(NH4)2S04A10  yg     96 gS04
                  = 0.06 x 10"4 m"1/(yg/m3 SOj)

 1 If we. use an accumulation mode bscat/V = 0.06 x 10~4 nH/ym3/cm3,  we obtain
  bscat/(vg/m3 S04) ranging from 0.034 to 0.046 x 10~4 m~Yyg/m3 depending
  on whether the sulfate is H2S04 or (NH4)2S04.

-------
                                    69
     >  Aerosol with a lognormal size distribution and a mass
        median diameter of 0.2 ym and a geometric standard
        deviation equal to 2.0 at RH = 0 percent.
     >  Index of refraction equal to 1.5 - Oi  (typical, non-
        absorbing aerosol).
     >  Density equal to 1.8 g/cm .
     >  Light of 0.55 pro wavelength.
     >  Sulfate as NH4HS04 (molecular weight of 115).

Figure 21 shows the striking agreement between our calculations and the
dependence of scattering-to-mass ratio on relative humidity observed by
Trijonis in the Southwest.  This agreement gives support to our calculation
method for the scattering properties of the secondary  aerosol.

     The computational procedure used in the visibility models  then takes
the input size distribution, assuming that the particles are  spherical
with an index of refraction of 1.5 - Oi, and computes  the scattering pro-
perties of the aerosol as a function of wavelength from the Mie equations.
The background size distribution properties are taken  from the  Whitby and
Sverdrup model of clean continental  aerosols (see Table 3).  The accumula-
tion mode in the plume is assumed to be the size of those measured in the
plume downwind of the Labadie power  plant near St. Louis.  The  properties
of the sulfates and other accumulation mode particles  are assumed to change
with relative humidity, as discussed above.  A more complete  inclusion of
relative humidity would require a modification of the  refractive indices and
a recomputation from the Mie equations.  This  modification could easily be
done later if desired.

     The limitations of the process  of specifying the  radiative properties
of aerosols are the usual ones:  uncertainties in the  size distribution,
nonspherical particles, and ambiguities in mean refractive indices.  How-
ever, the close agreement shown for  the sulfate scattering-to-mass values
suggests that the errors are not large.

-------
                                   70
     0.14
     0.12
     0.10
 o
 GO
CO
 I,  0.08
 2   0.06
   o
   CO
     0.04
     0.02
                    0.20
                   0
                                        0   CALCULATED VALUES


                                        *=>   TRIJONIS AND YUAN (1977)
                                              I
0.40        0.60

Relative Humidity
0.80
        FIGURE  21.  RATIO OF LIGHT SCATTERING TO MASS AS A FUNCTION
                   OF RELATIVE HUMIDITY

-------
                                   71
2.   Calculation of Light Intensity
                                 p
     The light intensity (watts/m /steradian) at a particular location in
the atmosphere is a function of the direction of observation n and the wave-
length >.  Calculation of the light intensity in a medium follows from the
radiative transfer equation.  This equation is a conservation of energy
statement that accounts for the light added to the line of sight by scat-
tering and the light lost because of absorption and scattering.   Approxi-
mations and solution techniques applicable to planetary atmospheres have
been discussed by Hansen and Travis (1974) and Irvine (1975).

     The physical situation that we are concerned with is shown  schemati-
cally in Figure 22.  To compute the spectral  light intensity at  the
observer, we sum (integrate) the scattered and absorbed light over the
path, r, associated with the line of sight n.  The resultant general
expression for the background sky intensity at a particular wavelength is
                                                       'T
                                                      e'   dT'
where
                                         r
              T = the optical  depth (T E^ b  .  dr,  where
                  is the extinction coefficient),
              w = the albedo for single  scattering  (w =  bscat/bext
                  where b   .  is the scattering coefficient),
           -»• n) = the scattering distribution function for the
                  angle n1  -> jj,
              I = the spectral  intensity at T'  from direct and
                  diffuse solar  radiation.

-------
72
                                  o.
                                  oo
                                  D_
                                  cc
                                  o
                                 oo


                                 5
                                 CJ

                                 OJ
                                 C3

-------
                                     73
Equation (51) is valid for the usual  continuum,  no refraction,  random
polarization assumptions.

     The intensity seen by an observer in direction n of an object at dis
tance R is:
        WB) -
                                                     )  dfi1  e"T   dT'     .   (52)
                              '=4TT
     Equations (51) and (52) then completely describe the spectral  intensity
of the background and an object.   Once these two quantities are known,  the
visual effects of the intervening atmosphere can be quantified.  In evaluat-
ing Eqs.  (51) and (52), we encounter two main difficulties:  First, the
quantity in the integral  is a fairly complicated function, and accurate
specification is tedious.   Second, the atmosphere is inherently inhomogen-
eous, and thus, the radiative properties w, p are somewhat complicated
functions of r and n.  Approximations are therefore necessary.   Appendix B
outlines in some detail the approximations we have used;  we present only a
summary here.  The approximations we used are the following:

     >  Plane parallel  atmosphere.
     >  Two homogeneous layers.
     >  Average solar flux approximation.
     >  Average diffuse intensity approximation.

The equation for the background intensity at the surface  becomes, for a
direction y, »

-------
                                    74
                                 _   Tdi f /n       0°° \               / r i\
                                 WOD !av   U  - e    )   '            (53)
and for the intensity in the direction of an object in the planetary bound
ary layer,
where
           o'  ,  Pnn(o)  = the average albedo and phase function
                         respectively,
                   Tnn = ^^e °Ptica^  depth of the path in the boundary
                         layer,
           F_   , I    = the average  solar direct intensity and diffuse
            s ,av   av
                         intensity, respectively,
              I .  , I  = the intensities from the upper atmosphere and
               S Kjr   0
                         object, respectively.

The exact definitions of the terms are given in Appendix B.

     Thus, the background intensity and the intensity in the direction of an
object at distance R from the observer can be computed given the following
inputs:

     >  Background radiative properties (e.g.,  size distribution,
        visual range).
     >  Solar zenith angle.
     >  Scattering angle.
     >  Direction of observation, n,  4>-
     >  Planetary boundary la^er height.

-------
                                     75
     The intensities, including the effects of air pollution,  are computed
from essentially the same formulae with the radiative effects  of the pollu-
tants included in the background atmosphere.  In the regional  model, the
intensity for a given optical path is calculated from an integration of the
concentration through the cells of the grid model.  For an initial approxi-
mation, we used the expressions for a homogeneous atmosphere.

     In the plume model, it was necessary to treat the plume as  a homogen-
eous layer with an optical  depth and mean properties 
-------
                                   76
     >  Coloration of objects.
        -  Brightness
        -  Hue and saturation.
     >  Contrast and color difference between two objects.
        -  Black object and horizon sky (to calculate
           visual range).
        -  Haze layers.
        -  Plume and background.

     The perception of an  object  such as a distant mountain  results  from
changes in light intensity, coloration, or both.   Visual  range  is  defined  in
terms of differences in light intensity (contrast)  between a  distant  black
object and the horizon sky.  Contrast is also a  useful  concept  for charac-
terizing the appearance of plumes and haze layers.   However,  a  plume  may
be perceived against a background as the result  of a color change  unaccom-
panied by a change in light intensity (i.e., with no contrast).  Ue  there-
fore need a means of characterizing the perception of changes in both the
intensity and the coloration of light.  We discuss the different means of
characterizing visibility impairment in the following subsections.

1.   Visual Range

     Visual range is defined as the farthest distance at which  a black
object can be perceived against the horizon sky.   As we have noted in
Chapter II, the threshold of perception of differences between  the light
intensity of two objects has been characterized  by a liminal  contrast.
The value of the liminal contrast is commonly taken to be 0.02, as first
suggested by Koschmieder in 1924  (Middleton, 1952).  However, the  liminal
contrast is a function of the observer and his state of mind (e.g.,  fatigue,
attentiveness) as well as  the intensity of the background lighting.   Under
the best conditions, the liminal  contrast may be as low as 0.005 (Committee
on Colorimetry, Optical Society of America, 1963).  The Federal Aviation
Administration assumes a value of 0.055.  Based  on an experiment using 10

-------
                                   77
observers and a total of 1000 observation hours,  Middleton  (1952)  reported
a median of 0.03 and a mode of 0.02 for the liminal  contrast.   For the  pur-
poses of standardization, it is reasonable to describe the  perception of a
"standard observer" and to select and use a single value for the  liminal
contrast.  We used the Koschmieder value (0.02)  for our calculations.

     It is clear then that the observation of distant targets  such as moun-
tains is not an accurate measurement of strictly  defined visual range,  i.e.,
the farthest distance at which a black object is  distinguishable  from the
horizon sky by a standard observer where liminal  contrast is 0.02.  This
is true not only because of the variability in the contrast threshold,  but
also because distant markers such as mountains are usually  not perfectly
black.

     The contrast between two objects is defined  as:
                               -    I2(x)          '

     If the two objects are the same color [i.e.,  I,(A)/Ip(x)  is  constant
over 0.4 <  A  <0.7 pm],  then the contrast  at all  wavelengths  will  be  the
same.  However, if the objects have different colors,  then C is a  function
of wavelength.   For the calculation of visual  range, we  evaluate  the con-
trast at a wavelength of 0.55 um,  which is at the  middle of  the visible
spectrum and is the wavelength to  which the human  eye  is most  sensitive.
The intrinsic contrast  of a black  object  (I,  =0)  against the  horizon sky
(\2 - Ih) is -1; the visual range  is the  distance  at which this contrast
is reduced by the light scatter and absorption of  the  intervening  atmo-
sphere to -0.02.  Thus, visual range can  be evaluated  by computing con-
trast iteratively as a  function of distance from the observer  until  it
drops to -0.02.  This approach is  necessary if one is  dealing  with a non-
homogeneous atmosphere.

-------
                                    78
     For a homogeneous atmosphere,  however,  the calculation of  visual
range is analytic, using the Koschmieder relationship:
                                    ext
For the computation of visual  range through a  homogeneous  atmosphere  con-
taining an optically thin plume,  Latimer and Samuelsen  (1978)  suggested
the following simplified approach:
               r  =
3.912 - £n -^  - T  I    .                 (57)
                v   bext-0

The second term in the brackets is  necessary to  account  for  the  effect of
light absorption caused by plume NCL on the contrast  between the horizon
sky (IhD) and the black object seen through the  plume.   It can easily be
shown that the effect of the plume  on visual  range  is significantly  less
when the plume is discolored  by NOo Uhp/Ih  < 1),  and greater when  the
plume is bright Ohp/Ih > 1).   As a corollary, it is  also true that  with
increasing distance between the observer and the plume,  the  impact of
plume N02 on visual range increases as plume coloration  decreases.   This
somewhat surprising result was confirmed in the  sensitivity  analysis of
the plume visibility code.

2.   Contrast of Haze Layers and Plumes

     Contrast can be used to characterize the perceptibility of  a haze
layer or a plume against a background—the sky,  a cloud, or  a distant
mountain.  A plume would be visible if the absolute value of the contrast
between it and the background were  greater than  a threshold  or liminal
contrast.  Figure 23 is a photograph of a plume  illustrating plume con-
trast.  The plume is clearly visible against the mountain because the
plume light intensity is greater than that of the mountain.   Thus, the
contrast of the plume against the mountain can be calculated using Eq.  (45):

-------
79
                                    o
                                    <
                                    Q.
                                   U.
                                   o
                                   ro
                                   C\J

-------
                                   80
                         C  . J^L-J^o    .                       (58)
                          H      m

     The plume is also visible against the horizon  sky,  perhaps  mainly
because of the color change, but also because of contrast:
                                                                    (59)
The magnitude and the sign of the contrast of a haze layer or plume against
a background is therefore a useful  way to characterize visibility impair-
ment.  Positive contrasts refer to plumes brighter than the background,
whereas negative contrasts refer to plumes darker than the background.   We
do not have any experimental data for liminal contrast (the barely percep-
tible threshold contrast) in the case of a plume against a background.   The
same liminal contrast used to define visual range (0.02) could be used  to
define plume visibility.  However, it seems likely that the liminal contrast
for plumes is greater than 0.02 because in many cases the boundary between a
plume and the background is not distinct owing to the nature of plume dilu-
tion.  It would be useful to carry out some experiments with several
observers and plume views to determine the liminal contrast for an average
observer.

     Contrast of plumes can be evaluated at several different wavelengths;
we used 0.55 ym for the evaluation of plume contrast.  However, plume con-
trast may be greater at the blue end of the visible spectrum.  Latimer  and
Samuelsen (1975, 1978) used the ratio of plume to background intensities
at the blue end (x = 0.4 ym) and at the red end (x = 0.7 ym) as a means of
characterizing the wavelength-dependent plume contrast and plume coloration
with respect to the background.  This blue-red luminance ratio is defined
as:

               I (0.4 ym)/I. (0.4 ym)   C,  (0.4 ym) + 1
          D = JL, _ '  " _ _  P        _                (60)
          K    Ip(0.7 ym)/Ih(0.7 ym)   Cp(0.7 ym) +1

-------
                                    81
The use of the luminance ratio  in  conjunction with the plume contrast at
0.55 ym is a simple way of characterizing plume  color.   When R  >  1,  the
plume is more blue than the background;  when R < 1,  the  plume is  redder
(or more yellow-brown); when R = 1,  with C (0.55 pm)  > 0,  the plume  is a
brighter white than the horizon, and with C (0.55 pm) <  0,  the  plume is
a darker grey.  We discuss more sophisticated methods of quantifying color
in the next subsection.

3.   Color

     The color associated with  a given spectral  light intensity distribution
is due to processes occurring in the human eye.   The  retina has three dif-
ferent frequency sensors that convert signals into color sensations  by means
of the brain.   The system operates so that an object  that  reflects half blue
light and half yellow light is  identified not as yellow-blue, but rather as
a new color, green.  This attribute  of the eye-brain  system gives rise to
another mode of detecting an object, that of color change  or discoloration.
Thus, an object can be perceived because it has  a different brightness from
that of the background (contrast)  or because it  has  a different color (so-
called color contrast).  Gases  and particles in  the  atmosphere  can give rise
to coloration by their scattered light (blue sky or  white  clouds) or by
altering the color of objects seen through them  (brown coloration due to NO?).

     The chromaticity diagram was  developed to quantify  the concept  of color.
In such a diagram, the spectral  distribution of  light is weighted with three
functions corresponding to the  detectors in the  eye.  For  any distribution
of light, there are three numbers, which define  a point  in  space.  Next, the
projection of the point onto a  unit  plane (x + y + z  = 1)  is computed.  The
result is a two-dimensional  surface  called a chromaticity  diagram (see
Figure 24).  Monochromatic light forms the outside of the  surface, and white
light is located in the center.  Any color can thus  be represented by its
chromaticity coordinates (x,y),  which are defined by:

-------
                               82
  0.80 —
  0.70 —
                                     .0.555
>,0.4C—
  0.00
                                                  GREENISH YELLOW

                                                    YELLOW
                                                   A58^-ORANGE YELLOW
                                                       .585
         °-49 Y  GREENISH
                BLUE
      0.00    0.10
                                                               REDDISH ORANGE
                                                                      0.70 ym
0.70
                        FIGURE 24.  CHROMATICITY DIAGRAM

-------
                                   83
                  X=X+Y+Z    '    y   X+Y+Z

where
                           X = / I(A) x dA
                               A
                           Y =/  I(x) y dA
=J
                                 I(A) Z dA
                               A
and I (A) is the wavelength distribution of light and x, y, z are the three
weighting functions.  The weighting functions (called tristimulus values)
are shown in Figure 25.

     Horvath (1971) and Husar and White (1976)  computed chromaticity coor-
dinates of atmospheric scattered or transmitted light and  showed that the
light would be distinguishable from white light for various sun  angles,
aerosol properties, and NfL concentrations.   Since the chromaticity dia-
gram does not differentiate between differences in intensity (e.g., between
yellow and brown or between white, grey,  and black), chromaticity coordinates
must be used in conjunction with a descriptor of light intensity for a com-
plete specification of color.  Thus, if we establish a color solid by taking
the two-dimensional chromaticity diagram and adding a third dimension per-
pendicular to this plane to represent brightness, we have  a means of com-
pletely specifying by three coordinates the color and intensity  of a color.

     Figure 26 is a drawing of such a color solid.   The brightness in such
a coordinate system is usually specified by the value of Y [see  Eq. (61)]
or by a parameter (L*), which is directly proportional  to  the subjective
perception of brightness and is related to Y as follows:

-------
                          84
   O)
   3
   a
   3
   I/)
   •r—
   $-
           400
 500        600

Wavelength, x  (nm)
      Source:  Judd and Wyszecki (1975).
FIGURE 25.  SPECTRAL TRISTIMULUS VALUES x(x), y(x), z(x)

-------
                                    85
                        L* = 25 Y1/3 - 17
(62)
L* is used in quantifying color differences and is  simply the parameter
called "value" in the Munsell  color system multiplied by 10.
                                                      VALUE
                                                      (brightness)
                                              CHROMA
                                              (saturation)
         Source:  Munsell  Color Company (1976).
              FIGURE 26.    REPRESENTATION  OF A COLOR  SOLID
     The Munsell  color system is the most widely used means  of  specifying
colors.  In this  system, colors are arranged  in  order by  value  (brightness),
hue (the shade of color, for example, yellow,  red,  green,  blue),  and  chroma
or saturation (the degree of departure of a given hue from a neutral  grey  of
the same value).   By specifying a given hue,  value,  and chroma, one can
obtain a sample color chip from the Munsell  Book of Color that  corresponds
to the specification.   By this  means, the objective  specification of  color

-------
                                  86
(L*,x,y) can be related to the subjective perception of color by visually
examining the color paint chip.   ASTM Standard D 1535-68 (American  Society
for Testing and Materials, 1974) is the reference method for converting
objective color specifications (L*,x,y) to the Munsell  hue,  value,  and
chroma notations by which a colored paint sample can be selected.   We
used this method to convert light intensity (Y or L*) and chromaticity
coordinates (x,y) calculated by the plume and regional  visibility models
to Munsell notation to be used by a commercial artist in illustrating
atmospheric discoloration.  We discuss this process  in  Chapter IV.

4.   Color Changes

     The final step in the quantification of visibility impairment  is the
specification of color differences—differences both in chromaticity (x,y)
and brightness (Y).  In 1976 the Commission Internationale de 1'Eclairage
(CIE) adopted two color difference formulae by which the perceived  magni-
tude of color differences can be calculated.  Color  differences are speci-
fied by a parameter A£, which is a function of the change in light  intensity
or value (AL*) and the change in chromaticity (AX,Ay).   AE can be consid-
ered as a distance between two colors in a color space that is transformed
in such a way that equal distances (A£) between any  two colors correspond
to equally perceived color changes.  This suggests that a threshold (A£Q)
can be found to determine whether a given color change  is perceptible.

     Since the CIE could not decide between two different proposed  formulae
for AE, both were adopted in 1976 as standard means  by which color  differ-
ences can be specified.  These color differences, which are labeled
AE(L*U*V*) and AE(L*a*b*), are calculated as follows:

              AE(L*U*V*) * [(AL*)2 + (AU*)2 + (AV*)2]
where

-------
                                    87
          L* = 116 (Y/YO)I/S - is,
          U* = 13W*(u - U0),
          V* = 13W*(v - v0),
and u and v are defined as
                    -       4X                 _       6Y
                  U   / u ',  l rw i  l-> \     s    V
and u~, v0 as
                      (X + 15Y + 3Z)    '    v   (X + 15Y + 3Z)
                          4XQ                           6YQ
              U0 " (XQ + 15YQ + 3ZQ)   '     V0 " (XQ + 15YQ + 3ZQ)
Similarly,

              AE(L*a*b*) = [(AL*)2 + (Aa*)2 + (Ab*)2]

where L* is defined as above and

                               Ky \1/3   , v \l/3-|
                              — I    - (~\
                              A0/      \rO'   J
                              .0    " (zn)
In these equations, the tristimulus values X0,  YO,  Zfi define  the  color of
the nominally white object-color stimulus.  In  our  atmospheric  discolora-
tion calculations, we used values of Xfl, Y,,, Z- corresponding to  the
reflected intensity from a perfectly diffuse reflector normal to  the  direct
solar beam.   Calculations are normalized such that  Yn = 100.

     To determine the liminal or threshold (just perceptible) value of AE,
we computed  AE for two color fields with identical  chromaticities
(AU* = AV* = Aa* = Ab* = 0) and with a contrast of  0.02 (i.e.,  Y2 =
as:

-------
V3,                    ,v J/3
      - 0.981/3^ -
                                           3) -  0.78 (
Thus, for a bright horizon (say, Y,  = TOO),  we obtain  a  threshold  or  liminal
AE equal to 0.78.  This value can be compared with  a AE  =  10,  which is  the
difference between two colors having identical Munsell hue and chroma but
with values differing by 1.   Thus, AE can be used as indicator of  atmo-
spheric discoloration: AE's less than 1  would be imperceptible,  those  between
1 and 10 would be detected as a discoloration by most  people,  and  the sever-
ity of discoloration would increase with increasing AE.  More  work is clearly
necessary to determine what the standards of atmospheric discoloration
should be.

-------
                                  89
              IV   THE  OUTPUT OF  VISIBILITY  MODELS
     This chapter discusses the outputs from several  sample  calculations
using our regional and plume visibility models.   The  models  are  described
from the viewpoint of a person who will  be faced  with regulatory,  siting,
and design decisions based on the output of such  models.  We provide
samples of graphic display alternatives that can  be used  to  translate
quantitative descriptions of visibility impairment  into color samples,
perspective views, artist's renderings, and color television video displays,
These display techniques enable the user to understand the meaning of
visibility impairment models.   Further details of the models and sample
outouts are given in Appendices D, E,  F, and G.

     The following models are illustrated by examples:

     >  Plume visibility model.
        -  Emissions from a hypothetical 2250 Mwe coal-fired
           power plant meeting New Source Performance Standards.
        -  Emissions from a large copper smelter  in Arizona.
        -  Emissions from a large coal-fired power  plant  in
           Arizona.
     >  Plume/terrain perspective and  color graphic displays--
        emissions from a large coal-fired power plant in  Arizona.
     >  Regional  visibility model.
        -  1976 and 1986 SOV and NOY emissions from sources  in
                           A       A
           the Northern Great Plains.
           1973 SOV  emissii
                  A
           and New Mexico.
-  1973 SO  emissions from copper smelters  in  Arizona
          A

-------
                                     90
A.   THE PLUME VISIBILITY MODEL

     The plume visibility model predicts the visibility impairment
resulting from emissions from a single source, such as a power plant or
smelter . The model calculates the reduction in visual range caused by
the plume for several observer locations, and it also calculates plume
color, plume contrast, and color changes to determine whether the plume
can be distinguished by an observer.   In this latter regard, the plume
model differs from the regional model, which calculates the visual effects
of a relatively homogeneous atmosphere.  The plume model quantifies the
coloration and appearance of a plume in comparison with the homogeneous
background atmosphere and thereby characterizes the perceptibility of the
plume.  The logic flow, program structure, and data requirements of the plume
visibility code (PLUVUE) are presented in detail in Appendix D.   In this
section, we illustrate and discuss sample outputs of the model.

     The user of the model must provide the source emission parameters,
ambient meteorological conditions, ambient air quality, and background
aerosol size distribution parameters.  Exhibit 1 lists the parameters of
the sample calculation done for the hypothetical 2250 Mwe coal-fired power
plant, which was assumed to emit particulates, S02> and NOX at the maximum
rates permitted by the EPA's New Source Performance Standards.  The user
must also select the dispersion coefficients (oy, az) to be used to com-
pute plume dilution as a function of downwind distance.  The code has
subroutines for Pasquill-Gifford and for TVA dispersion coefficients, and
it will also accept values entered by the user.

     After computing the initial plume dilution and N0£ formation during
plume rise from the stack to the location of final plume rise (1.2 km
downwind), the code calculates pollutant concentrations within the plume
and parameters characterizing plume visual impact at distances from 1.2
out to 350 km downwind of the source.  Exhibit 2 presents an example of
the pollutant concentration parameters that are printed out at each down-
wind distance.  In that exhibit, both the plume increments and the total

-------
                                        91
                            a  
   E
   a

               5
               SB
                          74
                  -s
               I  I
               •   i
               ^   «
       g
                       i    !
                       b.    fc
                              I
                                   5?
                          i   i   **
                          §   5   S
                                       I

                                       c
                              g
i
t
i
*
3
                              B   P   s
   W®

   ••w
c;
          I
          a
   E    S
                                                                  H- O
                                                                  rs z
                                                                  Qu O
                                                                  i— o

                                                                  O h-
                                                                  Q CO
                                                                  o z:
                                                                  z: <

                                                                  LU O
                                                                  s:^
                                                                  Z3 
-------
                   92
I
-1
i P
i I
     K


     S>
I i
                               T3
                               
-------
                                            93
                           nt-    «"-
                                          **
                                          »h^
                                                                                 O



                                                                                 O
                                                                                 O
                                                                                 o.
                                 ace
                                 n ic
                                                                                 D.



                                                                                 O
                                                                                 UJ
                                                                                 o
»i
e
         gg

         > >•
                  > i*   ww    Wrt    tr tj    co rs   rort   $ *~

                  "&i   **    C5C5    »•*-    COK1   <"<>   V®

                  1J   C4d    W P5    C4 W    CO C?   W W   41 **5
                  >e   coco    --    --    --   coco     i-
                                                              H

                                                              E
           I
                                                                                 UJ
I  g
a  »

II
              fw-
              OC
          -a.  e£

                    4» »
   «, .  . .  «,
    ' & *9 9     N ^    COCO
   vW^*0     OiC    cOrt

              I     55   SS   si    9S    55    II
           I


           I

           I
           P
                                                                                    CO
                                                                                    I—I
                                                                                    :c
                                                                                    x
   13
      !>-N3
             J*  S

       5£«im££
    JJ-rfeg  ^
                         £^l
                               nr
                                                              «i

                                                              S
                                                                       CL,


                                                                       >•


-------
                                  94
ambient concentrations are displayed.   The mole ratios of sulfate to
total sulfur and NC^ and nitrate to total  nitrogen are also displayed,  as
are the concentrations of ozone and the plume ozone deficit resulting from
NCL production.   The plume increment and total particle scattering coef-
ficient (bsp at 0.55 ym) are printed out,  as is the percentage of b   con-
tributed by secondary aerosol  (SO^, NO^).   Note that in the example given
in Exhibit 1, at 10 km downwind, sulfate--which is assumed to form at the
rate of 0.5 percent per hour—contributes  46-1 percent of the plume scat-
tering coefficient, the remainder of the scattering is due to the emitted
primary particulate matter (fly ash).

     Exhibit 3 provides the first of the three visual  effects printouts
that the user can choose to display for each downwind  distance.   These
computations are done for sight paths  through the plume center and can  be
done for ground-level sight paths as well.  Visual effects can be dis-
played  for scattering angles 0 selected by the user (22°, 45°, 90°, 135°,
and  180°); only  180°  (back scatter) calculations are shown in Exhibit 3.
Visual  effects are calculated as a function of assumed observer location
relative to  the  plume.  Observer location is  specified by the distance
(along  the sight path)  between the observer and the plume at distances
that are 2,  5, 10, 20,  50, and 80 percent of  the  background visual range
and  at  four  azimuthal angles with respect to  the  plume centerline
(a = 30°, 45°, 60°, and 90°).

      In Exhibit  3,  the  first  parameters printed  out are  the  visual  range
 rv and the  percentage reduction  from  background  visual range.  The follow-
 ing  two columns  are  the light  intensity parameters  Y  and L*,  described in
 Chapter III.  The  chromaticity  coordinates  (x,y)  are  then  displayed,
 followed by two  columns showing  the differences  in  light intensity
 (AY, AL*)  between  the plume  and  the background sky  (without  clouds).   The
 negative values  in this example  indicate  that the plume  is darker than
 the  background  sky.   The plume  contrast  (at  X =  0.55  ym) is  shown next,
 succeeded  by the blue-red ratio.   The change  in  chromaticity coordinates
 between the plume  and the background  sky  is  shown next (AX,Ay).   Positive

-------
                                    95
            §n n P?

             . . .
       >•
-»*CI   ««S« —
            -* eo g ^ « ee n N r- •»

                                                           
-------
                                   96
Ax's and Ay's indicate a shift toward yellow-brown,  and negative values
indicate a shift toward blue relative to the horizon.   The final  two
columns are the CIE color difference values AE(L*U*V*) and AE(L*a*b*).

     To understand how the values in Exhibit 3 can be used to characterize
plume color, consider an observer's sight path that  is perpendicular to
the plume (a = 90°) at a distance rp/rvQ = 0.02.   An L* of 82.23 indicates
that the plume is bright, but not as bright as the horizon because AY,
AL*, and C are all negative.  The chromaticity coordinates (0.3181,0.3253)
used in conjunction with L* (which is 10 times the Munsell "value") specify
the Munsell color notation, which in this case is 2.5 Y 8.912/0.6, a
weakly saturated yellow, essentially grey.  The blue-red ratio of 0.9194
also indicates a slight, but perhaps not visible, yellow discoloration.
However, the contrast of -0.1611 and the AE values of 10.6 and 6.8 indicate
that the plume would be visible because it is darker than the background
horizon sky.

     Exhibit 4 shows the visual effects of the plume  for  nonhorizontal
sight  paths when  viewed against a background of blue  sky.  Note that
visual effects are calculated for the permutations of a (azimuthal angle
relative to the plume centerline) and elevation angle 8 (15°, 30°, 45°,
60°, 75°, and 90°).  These  calculations indicate that the plume is more
distinctly visible against  the blue sky background than it was against
the horizon sky (Exhibit 2).  Note also that the plume is much brighter
than the blue sky background because AY, AL*, and C are all positive.

     Exhibit 5 completes the characterization of plume visibility at a
given downwind distance by comparing the light intensity of the plume with
white (representative of a white cloud or snowbank), grey, and black back-
grounds at various distances from the observer behind the plume.  The
plume appears somewhat darker and bluish in front of the white object
(REFLECT = 1) and brighter than the black objects (REFLECT = 0) at close
distances.   The plume appears slightly darker than black objects at long
distances because the apparent light intensity of the black object distant
from the observer approaches that of the horizon.

-------
                                                  97
                     3««e)«te + «aei*n««
                     ®co«. — (8«w + NN + -+4<
                     c?**p)gioc3egcoi'?M
               j
               H
               A
                                                                             O
                                                                             M
                                                                             o
0.

I
                                                                             o;
                                                                             o
                                                                             u_

                                                                             oo
               v    9 OIO
               <    i£''#1*
               U    « CO CO IT) » 9 <) * 03 C5


               ^    d f> t«- QCO » ••
                                                                             I/O
S


I

|


g
 *   V    ••*  S
u                   CO «9 «• <» IO * « ^»b- K5 * * C- >

-j   E               w— ' '  '  '<>i-       '-
                                                                             o
                                                                             
-------An error occurred while trying to OCR this image.

-------
                                    99
     The large amount of output required to characterize the visual impact
of a plume at a given downwind distance is necessary because of the large
number of possible observer locations, sight path orientations, and back-
ground objects.  We have an optional printout table for plume visual
effects for only one given observer location for user-contributed values
of rp and a.  This output option is useful for describing a plume for an
artist's rendering, as discussed in Section B.

     We have designed a computer plot package to display plume visual
effects for horizontal sight paths as a function of distance.  Examples of
these computer plots are shown in Figures 27 through 35.  Four parameters
were selected that most easily characterize (with numbers) the visual im-
pact of a plume:

     >  Percentage reduction in visual range.
     >  Blue-red ratio (plume color relative to background).
     >  Plume contrast (plume light intensity).
     >  AE (L*a*b*) (plume perceptibility).

We have selected these plots to show the visual effects seen by an observer
situated at distance rp = 0.02 x ryQ and with a horizontal sight path per-
pendicular to the plume center! ine.

     Figures 27 through 32 show the results of a sensitivity analysis to
determine the effect on plume visibility impairment of:

     >  Plume diffusion.
        -  Distance downwind (1.2 km < x < 350 km).
        -  Atmospheric stability (Pasquill C,  D, and E).
     >  Scattering angle (0 = 45°, 90°, 180°).
     >  Sulfate formation (0 and 0.5 percent per hour).
            (0 and 0.7 lb/106 Btu NOX emission rate).
     The effect on visual range of the 3.4 ton/day primary particulate
emission rate assumed here (less than the 0.1 lb/10  Btu standard in order

-------
                                       100
  60.0


  SQ.O


  40.0


  30.0


  20.0


  10.0


  0.0




  1.1
 B

 ii.o
 a
 j

 JJ0.9

 j
 a
  0.8
  0.7
  0.1
  -o.i
U

1-o.a
  -0.3
  15.0
  10.0
   S.O
   0.0
                                 (1! NBRHRL NBX EMHSiaNS; 0.5 PERCENTER ?;..,_--
                                 (2) MBRMfiL HBX EMI3SI0NS; N« SULFHTE F0RHHTI0N
                                 (3i HB HBV EMISSIONS: o.s PERCENT .'HI? SULFHTE FT
                                 «) NB NBX EHISSIBN3: N8 SULFflTE F£lPMCiTI8U
                         I  ill
                                 10       20      40   60
                                 OfMNHIND DISTANCE  (KM)
                                                            100
                                                                    20-
       FIGURE 27.   CALCULATED PLUME  VISIBILITY  IMPAIRMENT
                      FOR A  HYPOTHETICAL 2250  Mwe  COAL-FIRED
                      POWER  PLANT  WITH A  LIGHT SCATTERING
                      ANGLE  OF 45° AND STABILITY  CLASS C

-------
                                     101
  60.0

z 50.0


r°'°
,,,30.0



SIlO.O

   0.0


   1.1

 = 1.0
 a
 ui
 ^ 0.9
                                  (11 NBRHSL N0X EHI33I0NS: 0.5 "ERCENT •-is 5!.!,_-;7- -jif|.!;T;ti|,,
                                  (21 N8RMRL NBV EMI5SI0NS; N8 3ULFSTE FBRMPTI«-tj     /
                                  13) N« NBS EHIS31BNS: 0.5 PERCENT/HR TilJLffiTE "T -TlflN
                                  (4) MB NST' EMfSSIBN?: KB SULFfiTE
   0.8
  8:1
  -0.0
  -0.2
  -0.3
  JS.O
  10.0
ui
a
  S.O
  0.0
                                 10       20       40
                                 DMNHINO OIBTRNCE (KM)
                                                             100
                                                                     200
      FIGURE 28.    CALCULATED  PLUME VISIBILITY  IMPAIRMENT
                      FOR A HYPOTHETICAL  2250 Mwe COAL-FIRED
                      POWER PLANT WITH A  LIGHT SCATTERING ANGLE
                      OF  45°  AND  STABILITY CLASS D

-------
                                     102
  60.0
                                 (I) NBPHRL NBX EHI3SIBNS! 0.5 FEfCEfiT.'KS SJAF;,-::
                                 (21 NBRHBL NBX EHISSIBNS: NB SULFflTE FBRMST;?'.!
                                 (3) H8 N8X EHISSIBNS; 0.5 PERCENT/HR SULFflTE ff
                                 (41 NB NBX EHISSIBNS: NB SULFflTE FBPHRTI3N
z 50.0 -


  40.0 -


  30.0 -


  20.0 -


  10.0 -


   0.0
   1.1
   1.0
   d.9
   0.8
  -0.0
  -0.3
  15.0
  to.o
   5.0
   0.0
              I     I	I   I  i  I I
                           6     10       20       40   60    100
                                 DWNMIND DISTANCE (KM)
     FIGURE 29.   CALCULATED PLUME  VISIBILITY  IMPAIRMENT
                    FOR A HYPOTHETICAL 2250 Mwe  COAL-FIRED
                    POWER PLANT WITH  A LIGHT  SCATTERING ANGLE
                    OF 45° AND STABILITY  CLASS E

-------
                                        103
  60.0


x SO.O
5 20.0
u

2 10.0

   0.0



   1.1


 £ i.o
 i 0.9
  0.8
   8.7
   .1
 . -0.0
8-o.t
  -0.2
                                  (1) MBRMRL NBV EHI33I3N3; 0.5 PERCENT/MR SULFflTE FBRHRTiaH
                                  (2) NBRHRL NflX EHISSI8NS; H9 SULFflTE F0RKHTI0N
                                  (31 N0 N8)t EMISSI8N5: 0.5 PERCENT/HR SULFflTE FBRHSTIBN
                                  It) NB NBX EHISSIBNSi NB SULFflTE FBRHRTIBN
  -0.3
  1S.O
  10.0
  6.0
  0.0
                                 10       20       40   60
                                 (MMNHtNO DISTANCE (KM;
                                                            100
                                                                    ZOO
     FIGURE  30.   CALCULATED PLUME  VISIBILITY  IMPAIRMENT
                    FOR A HYPOTHETICAL 2250  Mwe  COAL-FIRED
                    POWER PLANT WITH  A LIGHT SCATTERING  ANGLE
                    OF 90° AND STABILITY  CLASS C

-------
                                      104
  60.0


  50.0


  40.0


  SO.O


  20<0


 UlO.O


   0.0




   1.1



 I 1.0
                                 (1) NBRMflL MBS EHI35IBN5: 0.5 FERCENT/HR SULrfiTE F3f»KJ
                                 (2) NBRMflL NBX EHIS5UNS: MB SULFflTE FBRMflTISN
                                 (3) NB HVt EHISSIBNS: 0.5 PERCENT/HR SULFfiTE FBRHflTiaN
                                 (4i NB NBX EHISSIBNS: NB SULFRTE FBRMSTIBN
   0.8
   0.8
  8:1
  -0.0
 1-0.1
 • -0.2
  -0.3
  15.0
                                                    1	i	J I 1^ 1
  10.0
I
   5.0
   0.0
                                 10       20      40   60
                                 MHNHIW OI6TANCE  (KH)
                                                            100
                                                                    200
    FIGURE 31.   CALCULATED PLUME  VISIBILITY  IMPAIRMENT
                   FOR A  HYPOTHETICAL 2250 Mwe  COAL-FIRED
                   POWER  PLANT WITH  A LIGHT  SCATTERING ANGLE
                   OF 90° AND STABILITY  CLASS D

-------
                                      105
  60.0


  50.0
£30.0
>
5 20.0
u

Kio.o


   0.0
   I.I
  I

  : 1.0

  I

  , 0.9
                                  II! NBRHflL NBX EHI3SI8NS; 0.5 PERCEHT/HR SULFfl'E FOf rinT
                                  (2) NBRHflL N8J EHISS18NS; N8 3ULFRTE FBRHBTIBH
                                  (3) NB N8X EHI3SI8N5:  0.5 PERCENT/MR 3ULFHTE FBRH^TIBN
                                  (4) NB HBX ENIS3IBNS;  MB 3ULFSTE F0RMBTI8N
   0.8
  -0.0
 I -0.1
  -0.2
  -0.3
  15.0
                                                    I   I I  I  I I
  10.0
u


I
  5.0
  0.0
                                 10       20      «0
                                 DWNHINO DISTRNCE (KM)
                                                            100
                                                                    200
     FIGURE 32.
CALCULATED  PLUME VISIBILITY IMPAIRMENT
FOR A  HYPOTHETICAL 2250 Mwe COAL-FIRED
POWER  PLANT WITH A LIGHT  SCATTERING ANGLE
OF  90°  AND  STABILITY  CLASS E

-------
                                    106
 60.0

 50.0

 10.0

 ao.o

 20.0

 lO.O

  0.0



  1.1
                                (1) N0RHHL N0X EHI3SI0N3J 0.5 PERCENT/HI! %F«Tc
                                (2) N0RMHL NBX EMI3SI8HS: N8 3ULFATE F0RHRTI0N
                                O) MB NBX EMISSIONS; o.s PERCENT/HI! SULFRTE Fen
                                (4) M0 NflX EMISSI0NS: N8 SULFRTE FBRHATI0N
S

I'
  0.8
   8.7
   .1
 -0.0
! -o.i
• -0.2
 10.0
  S.O
  0.0
                                10       20       40
                                OWWHIHD DISTflNCE (KH)
                                                           100
200
    FIGURE 33.   CALCULATED  PLUME VISIBILITY  IMPAIRMENT
                   FOR  A HYPOTHETICAL 2250 Mwe COAL-FIRED
                   POWER PLANT WITH A LIGHT  SCATTERING ANGLE
                   OF 180° AND STABILITY  CLASS C

-------
                                      1U7
  60.0


xSO.O


§40.0
o
£
.,30.0
>
5 20.0


£ to.o


   0.0



   1.1


 § 1.0
 £0.9
   0.8
 .-0.0
 [-0.1
 • -0.2
  •0.3
  15.0
                                  (1) NBRHSL NB» EMISSIBNS! 0.5 FERCENT/HR SULFfiTt FBRHRT18N
                                  (2) HBKHRL N0X EHISSIBN3; Ng 3ULFHTE FBRMBTIBN
                                  (31 Ng N8X EM1SSI8NS! O.S PERCENT/HR SULFflTE FBRHflTIgN
                                  (4) N8 N8X EHISSIBNS; N8 SULFfiTE FBRMBT10N
  to.o
ki



I
  s.o
  0.0
                                 10       tO       40
                                 DMNNIND DISTANCE (KM)
                                                            100
                                                                     JOO
    FIGURE 34.   CALCULATED PLUME  VISIBILITY  IMPAIRMENT
                   FOR A HYPOTHETICAL 2250  Mwe  COAL-FIRED
                   POWER PLANT  WITH  A LIGHT SCATTERING  ANGLE
                   OF 180° AND  STABILITY CLASS  D

-------
                                     108
  so.o

z SO.O

^ 40.0

^30.0
>
5 20.0
s
£ 10.0

   o.o


   1.1

 I 1.0
                                 (1) NBRHflL N8I EHI33I8N5: 0.5 FERCENT/HR SULFSTe FSifwaT
                                 (21 ttflRHflL N8T EM1S3IBN5: N0 3ULFRTE FBRHATI0N
                                 (3) NB M«X EMISSIBN5: 0.5 PERCENTER 3ULFBTE FPRHflTISH
                                 (4) NB NBX EMISSIONS; NB SULFPTE FBRHRTIBN
 g
 A
   0,8
  -0.0
 1-0.1
 • -O.Z
  to.o
5
s
   E.O
   0.0
                                 10       20       <0
                                 DWMMINO D1STRMCE (KM)
                                                      60
                                                            100
                                                                    £00
      FIGURE 35.    CALCULATED PLUME  VISIBILITY  IMPAIRMENT
                     FOR  A HYPOTHETICAL 2250  Mwe  COAL-FIRED
                     POWER PLANT  WITH A LIGHT SCATTERING  ANGLE
                     OF  180°  AND  STABILITY CLASS  E

-------
                                   109
order to meet the 20 percent opacity standard) is apparent in these figures,
particularly for stable atmospheric conditions (Pasquill E).   However, the
significant reduction in visual range caused by primary particulate is
noticed only at short downwind distances.  All these effects  are for sight
paths through the plume centerline.  At large downwind distances, the
effect of sulfate on visual range becomes very Significant, particularly
for stable conditions.   Indeed, the reduction in visual range increases
with increasing downwind distance between 60 and 350 km downwind.*  The
scattering angle has a  small but not negligible effect on visual range:
Visual range increases  with increasing scattering angle.  In  other words,
the reduction in visual  range is greatest for forward scattering.

     Plume coloration and contrast are indicated by the values of the blue-
red ratio, plume contrast (at A - 0.55 pro), and the CIE color difference
parameter AE(L*a*b*).  The effect of NO^ on plume coloration  becomes clear
when the curves (Nos. 1  and 2) that assume normal NO  emissions are com-
                                                    X
pared with those curves  (Nos. 3 and 4) that assume no NOX emissions.
Yellow-brown coloration, as indicated by blue-red ratios less than 1.0, is
stronger with N02 than  without.   Note that the effect of sulfate (Curve 3)
on color is very small  for all scattering angles; however, sulfate has a
significant effect on plume contrast, increasing plume brightness at small
scattering angles and decreasing plume brightness at large angles.  Compar-
ing Curves 1 and 2, we  can see that the pronounced coloration caused by N02
during stable conditions (E stability) is reduced by light scattered by
sulfate.  If we use AE(L*a*b*) as an overall indicator of the perceptibility
of the plume (because of both plume contrast and color changes), we find
that N02 has the most pronounced effect on plume visibility at significant
downwind distances.  Sulfate has a significant but smaller effect, and'
primary particulate has the least effect.  Perhaps the most significant
result of these calculations is that plume visibility impairment  (both a
* A cautionary comment is in order here.  For this evaluation, the wind
  speed was assumed to be 5.0 m/s; thus, almost 20 hours would be re-
  quired for emissions to be carried 350 km.  It is unlikely that stable
  atmospheric conditions will persist that long.

-------
                                  no
reduction in visual  range and an atmospheric discoloration)  increases with
downwind distance, suggesting that a significant impact could occur hun-
dreds of kilometers  from the source.

B.   PLUME/TERRAIN PERSPECTIVE MODEL

     To supplement the quantitative description of plume visual  impact
described in Section A, we developed a Perspective Terrain Viewing Program
(PTVP).  Using computer graphics, this program is capable of displaying
views of plumes and  background terrain with the perspective  of the human
observer or camera situated at user-specified positions.  These plume and
terrain perspective  scenes can be used in conjunction with the quantifi-
cation of plume visibility impairment discussed in the previous section to
provide an understanding of the subjective impact of the computer predic-
tions.  In addition, these scenes, along with computed Munsell color nota-
tion, can be used by a commercial artist to produce color renderings of
the visual impression of the background atmosphere and the plume for
various assumed emission conditions.

     To use the PTVP, the user must provide the following information:

     >  Boundaries of the region in which the facility is situated
        or is to be constructed must be identified, and terrain
        within it must be digitized.  (The U.S. Geological Survey sup-
        plies digitized terrain elevations.)
     >  Design parameters of the facility that affect the effluent
        plume characteristics must be determined.  Among these are
        stack height, flue gas temperature, and flow rate.
     >  Representative meteorological conditions must be specified;
        important parameters include wind speed and direction,
        ambient temperature, lapse rate, atmospheric stability
        category, and the height of the inversion layer, if one
        is expected to exist.

-------
                                   Ill
     >  Observation parameters must be decided upon.  Among these
        are the location of the observer with respect to the
        facility, the direction in which he is viewing, and the
        field of view of the "conceptual camera" he is using to
        record the scene.  The last of these parameters is required
        because the PTVP uses the lens characteristics to reproduce
        the optics of a camera, "recording" by means of computer
        graphics the appropriate camera film image.  Lens "size"
        as measured by the cone-angle of the field of view may
        range from a few degrees (telescopic lens), to from 40° to
        50° (standard lens), to 90° ("wide-angle" lens), to 180°
        ("fish-eye" lens).

     The use of the PTVP can best be illustrated by means of an example.
Digitized terrain elevation data were obtained from the U.S. Geological
Survey for an extensive portion of the Southwest.  From this data base,
a 50 x 50 km portion of terrain immediately west of Page, Arizona, was
isolated.  A computer-generated plot of the terrain is presented in
Figure 36.  Among the prominent geographical features contained within.
that region are the Vermilion Cliffs, the Marble Canyon through which the
Colorado River flows, and the Paria Canyon.

     In this sample terrain grid, a plume from a hypothetical  power plant
was displayed and viewed from several different observer vantage points.
In the example, the power plant stack is 775 feet high, plume rise was
determined using values typical of a large coal-fired power plant, winds
were light and headed slightly south of due west (compass heading of 2556
and meteorological  conditions prevailed that are typical of Pasquill-Giffo'rd
Stability Category E (stable).   The plume was assumed to be Gaussian, with
its "envelope" defined by the locus of la dispersion coefficient values.

     The hypothetical observer in this example flew around the power plant
observing the power plant plume.   Using a "camera" having a wide-angle lens
(with a 90° field of view), the observer took a series of pictures.  The

-------
112
                             00
                             O
                             LU
                             CL.
                             OO
                              i
                             LU
                             Q_
                             a:
                             o
                             u.
                             oo
                             o
                              oo
                              ca
                              o
                              to

-------
                                   113
location of each picture is shown in Figure 36.  The sequence of pictures
is presented in Figures 37 through 51.   All views are directed at the
power plant, except for Figure 39, which is aimed west toward the Vermilion
Cliffs.

C.   COLOR DISPLAY TECHNIQUES

     The most complete and realistic display of predicted visibility impair-
ment, particularly atmospheric discoloration, is a plume-terrain perspective
view in color, with accurately specified and rendered colors calculated from
the plume and regional models.  We investigated two methods of displaying
atmospheric discoloration and plume visual  imp-set:

     >  A color illustration, drawn or  painted by a commercial
        artist, using Munsell specifications for plume and
        background color and plume and  terrain perspective
        views.
     >  A color video display, based on a photograph of a view
        from a vista, computer-enhanced to display a plume or
        homogeneous atmospheric discoloration on a color
        television.

Both of these methods, presented schematically in Figure 52, use the spec-
tral intensity I(A) calculated by the visibility models for specific lines
of sight as a base.

     These two display methods are the  most technically difficult, time-
consuming, and expensive output options available for visibility models,
but they may be the only ways of giving the user of models an understand-
ing of the calculated visibility impairment.  Without the aid of these
color display techniques, it is very difficult to translate numbers
describing visual  impact into an observer's actual visual impression.

-------
114
             c_>
             c
             o
             o:
             co


             UJ
             a;

-------
115
                      5
                      o
                      o
                      cc
                      CO

                      ro
                      UJ

-------
116
                                        CO




                                        o
                                        5
                                        o
                                        o
                                        CsL
                                        LU
                                        O1

                                        CO
                                        uu
                                        01

-------
117
                          s
                          o
                          o
                          or
                          o
                          
-------
118
                             LO


                             Z

                             o
                             o
                             e;

-------
119
                                        UJ
                                        I—t
                                        >




                                        C\J
                                        *3-

                                        UJ
                                        OL
                                        Z3
                                        CD

-------
120
                                r-.
                                o
                                i—i
                                h-
                                o
                                _i
                                o
                                co
                                UJ

-------
121

                     CO

                     2TT
                     o
                     O
                     O
                     o:

-------
122

-------
123
                                       •a:
                                       O
                                       o
                                      o:

                                      CD

-------
124
                                   5
                                   o
                                   o
                                   C£
                                   Lu

-------
125
                                         CVJ
                                         CJ
                                         o
                                         o
                                         c;
                                         UJ
                                         CO

                                         ^j-


                                         UJ
                                         cz

-------
126
                           co
                           o
                           o
                           01
                           UJ
                           o:

-------
127

-------
128
                                             
-------
129
                                               d.
                                               CO
                                               a:
                                               o
                                               o

                                               es
 o zr en 3E
 U-l I-H 2=  0.
CO




tn




CJ
i—i
u_

-------
                                  130
1.    Color Illustration

     This technique is a synthesis of the regional  and plume visibility
model outputs and the Perspective Terrain Viewing Program (PTVP)  illus-
trated in Section B.   The process requires the following steps:

     >  The source characteristics and location are selected,
        and the digital terrain data are obtained.
     >  The Perspective Terrain Viewing Program is used to
        generate a plume terrain view for a given set of
        meteorological conditions (wind speed, wind direction,
        stability category).
     >  The plume visibility model is run for the same set of
        source and meteorological conditions.  The coloration
        of various sight paths through the plume and the back-
        ground sky are predicted.
     >  Specific areas of the plume terrain view are assigned
        the appropriate Munsell color notation and associated
        color chips.
     >  A commercial  artist colors the plume terrain view.
        The color chips are used as a reference check on the
        artist's color display.

     To illustrate the capabilities and limitations of this technique, we
have constructed a test case that compares our predictions with the actual
visual impact of a power plant plume.  The comparison demonstrates the
need for carefully documented studies of the accuracy of the model.

     A test case should have the following attributes:

     >  A large point source with a visible effluent impact.
     >  Documentation of the source emissions (NO , S09,
                                                 }\    £
        primary particulates).
     >  Location near a nonurban area of great aesthetic value.

-------
                                  131
     For our test case, we selected a power plant in northern Arizona for
which we had color photographs documenting the visual  impact of the plume.
The source emissions and dispersion conditions have been studied,  but
these data were not available to us.  However, we were able to estimate
the source emission conditions from other similar power plant sources.

     The photograph we selected is reproduced in Figure 53, which  clearly
shows the brown coloration caused by the power plant plume.  We chose this
example because of the clearly apparent brown coloration.   However,  upon
closer inspection, one notices that the lighting conditions are somewhat
unusual because the photograph was taken very early in the morning.   The
sky is less blue than normal  and is slightly yellowish at  the horizon.  The
long shadows of the river canyons are visible, indicating  a very low sun
angle.  As noted in Chapter III and Appendix B, the diffuse component
(multiple scattered light) of the solar intensity becomes  significant
near sunrise and sunset.   Since the diffuse component is hard to model
correctly, particularly in extreme situations like this, this photograph
represents a difficult test case.

     For our estimation of the source characteristics and  meteorological
conditions, the Perspective Terrain Viewing Program was used to generate
a plume terrain view, which is shown in Figure 39.  A comparison of Figures
39 and 53 shows that the terrain and plume locations are rather faithfully
reproduced.  Although the resolution of the photograph is  much greater than
that of the computer graphics algorithm, the resemblance is clear.   The
distant mountains on the horizon (dark blue on the right-hand side of the
photograph) are not plotted because they were outside the  terrain  boundar-
ies of the program for this particular case.   The plume boundaries are
plotted at la (a ,a ) concentration values.   The vertical  extent of the
plume in the photograph is less than it is in the computer plot, suggest-
ing that the actual plume oz  was less than a  Pasquill  E stability.   Plume
concentration measurements would be required to substantiate this  assump-
tion, but the usefulness  of the PTVP is clear.

-------
132
                                      srs:
                                      C-
                                        0£
                                      1-0
                                      O LU
                                      O- 00
                                      I— o
                                        M
                                      U. i— l
                                      Si
                                      O LU
                                      o :n
                                      re o
                                      CO
                                      LO

-------
                                    133
     The plume visibility model was then run for our estimated source and
meteorological conditions.   The Munsell  color notation and associated
color chips for various parts of the plume terrain scene are shown in
Figure 54.  After comparing the color chips and the original photograph,
we concluded that the colors are reasonably close.   The yellowish color
of the horizon and the brownish color of the plume are reproduced, demon-
strating that the plume model is capable of predicting the brownish color-
ation and displaying it correctly to a user of the model.   The sky color
is approximately the correct saturation  and brightness.

     The results of the final step of having a commercial  artist paint in
the correct colors are shown in Figure 55.  The artist was never shown
the original photograph; he had to rely on the color predictions from the
plume visibility model.  Unfortunately,  we are less satisfied with the
results of this step than with the previous two.   The problems in this
step appear to be that:

     >  It is difficult to paint and blend the correct colors
        to maintain fidelity to the predictions.
     >  The spatial resolution necessary to produce a realis-
        tic scene is also difficult and  requires  a large amount
        of time.
     >  The artist has a natural tendency to paint what he thinks
        the plume should look like.

Despite these difficulties, we believe the technique has promise and should
be pursued, though more work on this step is needed.

     Overall, we are encouraged with the results  of the comparison.   The
significant findings were that:

     >  The Perspective Terrain Viewing  Program can generate
        a realistic plume terrain scene.

-------
134
                                            UJ
                                              "O
                                               Q-
                                            UJ
                                            I— a:

                                            UJ o
                                            (/)
                                            Qi
                                            LU i

                                            is

-------
135
                                     00
                                     CL
                                   l—o
                                   <— J
                                   u3o
                                   0:0
                                   OLU
                                   C/)Q
                                  ctro
                                  02:
                                  a.
                                  o >
                                  Is
                                  cc
                                  ^
                                  C3

-------
                                    136
     >  The plume visibility model can predict the plume
        coloration correctly.

It is important to emphasize that these findings are somewhat preliminary,
and testing must continue to verify computer models.  In addition,  more
information must be gathered so that other tests can be conducted.

2.   Color Video Display

     In addition to the color illustration described in the preceding
section, we investigated the possibility of using computer-generated color
display facilities.   This technique was originally developed for proces-
sing photographic data, particularly satellite data, and it requires
special equipment, including:

     >  A color densitometer to digitize a color photograph
        in three colors.
     >  Image enhancement software to allow manipulation of
        the digitized information.
     >  A color video display unit and supporting software.

Although these facilities were not directly accessible, we were fortunately
able to acquire the assistance of researchers at Los Alamos Scientific
Laboratory who have used this technique.   The Los Alamos personnel  utilized
this technique to predict visibility impairment from power plant plumes
(Williams, Wecksung, and Leonard, 1978).

     We sent Los Alamos the test case photograph (Figure 53), which was
then digitized into three colors.  Then the plume was removed from  the
digitized photograph by interpolating the sky intensity from the horizon
below the plume to the sky above it.  Next we gave the Los Alamos per-
sonnel the results from our plume model for specific locations in the
plume.  These intensities were displayed on the color video screen,
and a photograph was taken.  The results are shown in Figure 56.  This

-------
137
                                               o

                                               QL
                                               S
                                               i—i

                                               —I
                                               
-------
                                   138
figure is then an illustration of the color video display technique.   The
photograph can be compared to the test case photograph (Figure 53).
Because of compatibility difficulties between our computer output and the
Los Alamos facility, the results in Figure 56 should be considered as a
qualitative indication of the technique.

     The color video display is a very powerful  technique that gives  the
user a rendition of a photograph with the plume  effects superimposed.  The
technique is somewhat cumbersome, however.  Specifically, the difficulties
are the following:

     >  The hardware is expensive, available only at specific
        locations, and not available on a dedicated basis.
     >  It is difficult to transfer information  from the ori-
        ginal film to the final produced photograph without
        introducing errors.  In other words, a quantitative
        measure of the color fidelity of the process is not
        possible at present.  This difficulty is due mostly to
        the problems involved in film processing.

This description of the difficulties of the color video technique is  not
meant to be a criticism of the Los Alamos personnel and their work.   It is
simply a listing of problems that must be faced in using the technique on
a routine basis.

D.   THE REGIONAL VISIBILITY MODEL

     We have modified the Northern Great  Plains regional  grid model  (Liu
and Durran, 1976) so that it has the capability to compute regional  con-
centrations of N02 and sulfate.  We show  in this section  how these pollu-
tant concentrations can be used both to display visual range isopleths
for the region and to characterize atmospheric discoloration at specific
locations (Class  I areas) within the region.  We summarize the results of
sample calculations using 1975 and 1986 SO  and NO  emissions from point
                                          A       X
sources in the Northern Great Plains.  Also, using 1972 SOp emissions from

-------
                                   139
the copper smelters in Arizona and New Mexico, we constructed a hypotheti-
cal situation by assuming that these sources were located in the Northern
Great Plains.  The objective of that task was to study the effect of the
large SO  emission rates from the copper smelters (6000 tons per day) on
        X
regional visibility using the existing Northern Great Plains regional
model.  The significant impact of copper smelter SO  emissions on visi-
                                                   X
bility in the Southwest is indicated by the results of the data analysis
described in Appendix A and the regional  model calculations reported in
this section.  This impact suggests the need for a regional visibility
model  for the Southwest capable of handling the transport and diffusion
of copper smelter emissions as well as power plant emissions in complex
terrain.

     Figures 57 through 60 show the isopleths of S02, N02> and sulfate
concentrations and visual  range calculated using the regional grid model.
N0? concentrations were calculated using  the technique described in
Chapter III from total NO  emissions assuming a background ozone concen-
                         X
tration of 0.020 ppm.   Sulfate concentrations were calculated from SOX
emissions using a pseudo-first-order rate constant of 0.5 percent per
hour and assuming negligible primary sulfate emissions.   Visual range was
calculated from the Koschmieder relationship using the following value for
the extinction coefficient:
             bext =  (°'24 + °-04[s04' in M9/m3])(lO"4 m"1)
     With the assumed background SO^ concentration of 1.5 ug/m , this
expression gives bgxt = 0.30 x 10"4 m'1 , which corresponds to a visual
range of 130 km.  The bscat-to-mass ratio used here (0.04 x 10"4 nr1/
yg/m3) is appropriate for sulfate aerosol in the accumulation mode at
average relative humidity, and it is the average reported by Trijonis
and Yuan (1977) for the Southwest.
     The calculations of visual range (Figure 60) indicate that anthro-
pogenic emissions from point sources within the Northern Great Plains

-------
140
                                                 en
                                                   £
                                                  — I— 10
                                                        r--
                                                  oo a: CTI
                                                  z o •—
                                                  o u_
                                                     z a:
                                                     i— i a.
                                                  LU a.
                                                  O et O
                                                  o LU
                                                     o: I—
                                                     C3 OO
                                                  o    z:
                                                  oo z:
                                                     a: o
                                                  LU LU O
                                                     O O
                                                     Z O
                                                  O    O
                                                  :r z
                                                   I  •-( c^
                                                  LU    z:
                                                  LU CO O
                                                    oo o
                                                  — i to z
                                                  
-------
141




!:;'•


o
o.



0
O)'"



o.
td



0
r*"


o.
03

O.
Ml



O.




O.






o.
«M



O.
""*




or, oo u.'.


„- 	 	 -"'*"
: 	 "
"
•


.
•
•
P ..•"""<•
^?
,. -•'" ..- ' •.. t
:\ ".-•;""" \ [
.' .• * * " jt
\ *. '•••••.
''•». 	 -( •-„.., /
ft/ f
'.,. , /

*--o: """ - ' •'"
- t— *'• — , .-•*' '
- g 	 	 <
;g 	 .v-
:'•'*"""""
- cc
z
cc

" ^ .••'""
• x _.-•"
/•' .. •''
V, ..' ..
.* • .' *

' .*' ** •** f "'^t
. **" »*
•>:.!•••""' >

.• *" .•''
*' /*'

*'' .•-'""
• ' 	 .»••••"***
' '.3









00


^y


















T
1—
x:
 ^
0  SE 0
| 111 .W—
1 Ivi-f ^^
a: x:
ZD 1 — U.
-0 °..°
— • 1— 1
•n 00 O
— 1 CO Z
«=C I-H O
Z S 0
O UJ
_ t— < — 1
•2 C3 ^D  o r^
H-. O O
a LU uj
uj oo i—
OS 
.0 W
"" rs
CJ3
H!

06
QL     08
OS
       oe
01

-------
                                                        142
           06
                    09
OL
                            09
OS
ot
OS
OZ
01
o
o. -
o.
O>
o.
ID
O. .
   :•-•§
   »'tt i
B-!2
                                     i
                                     a
                                     tn
o. .
Ift
                           -•• ----------
O.
(O
      i—i
                                                                             <: en H- o:
                                                                              i ra «c Q-
                                                                             CC O UJ fS.
                                                                             •=>^&.
                                                                             O   CD VO
                                                                             :c a:
                                                                              I LU Z Z
                                                                             LU a. o: o
                                                                             LU   LU
                                                                                                             O
                                                                                                          _l C£.
                                                                                                          ^C I1'
                                                                                                          Z O-
                                                                                                          o
                                                                                                          i—i UO
                                                                                                          CD   •
                                                                                                          LU O
                                                                                                          a:

                                                                                                          a
                                                                                                          LU CD
                                                                                                                o
                                                                                                                •z. o
                                                                                                                   o
                                                                                                                LU r~-

                                                                                                                h- T
                                                                                                                   o
                                                                                                                z o
                                                                                  oo
                                                                                  z: u_
                                                                                  O O
                                                                                                           O i— « l~l
                                                                             a o
                                                                             LU oo
                                                                             0£ 00
                                                                             Q- —
                                                                                                     LUt-

-------
                                                       143
          06
03
o. .
en
o.
CD
o.
<0
o. .
ir>

                         Oi

                        9-Hf
                                    09
                                             05
                                                   Ob
                                                              oe
                                                                       o?
                                                             01
   ••••;> -on,   \
  ii
  ct
  o

- z
                                  *
                                  o
           6-	
           --.__„„.... 12D
                           021	
          "T»B •'"T
                                                              •ft
                                                              IT
                                                              CO
                                                              bJ
                                                                  130
          06
08
                                    09
                                          OS
                                                                                 a
                                                                                 o
                                                              3
                                                              s
                                                                    *o.§
                                                                                        . .o
                                                                                        ,4.0
Ok
06
0?
01
                                                                                          o
                                  /:.o
                                     «
                                                                                        . .o
                                                                                        . .a
                                                                                           21!
                                                                               LU CC

                                                                               gj

                                                                               Q
                                                                               UJ O
                                                                               o: oo
                                                                               O. r—
                                                                                                  o
                                                                                                  10
                                                                                                  UJ
                                                                                                  Q:
                                                                                                       LU •—i
                                                                                                       ar o;

                                                                                                       fc S=
                                                                                                       Q_. *^
                                                                                                       o
                                                                                                       UJ 2:
                                                                                                       re o
                                                                                                          oo
                                                                                                       00 O
                                                                                                       z o
                                                                                                       o r^-
                                                                                                       f—l r—
                                                                                                       OO  I
                                                                                                       oo o
                                                                                                       >-> o

-------
                                  144
cause only a small reduction in visual  range,  even with the increased
emissions projected for 1986.   Maximum visibility impairment (i.e.,
minimum visual range) occurs in only a small  part of the region.   Visual
range is predicted to be reduced from the background 130 km to about
100 km, approximately a 25  percent  reduction in visual  range.  This
small reduction would be difficult to measure, particularly using visi-
bility target observations, and to separate from  visibility impairment
caused by natural sources.   The calculated reduction in visual range in
the Northern Great Plains resulting from 1975  emissions is even smaller.
The results of calculations for 1975 emissions are presented in Appendix G.

     Anthropogenic visibility impairment is significant in the Southwest,
however, as indicated by the analysis of visual range data presented in
Appendix A and summarized in Appendix B.  In southeastern Arizona, copper
smelters emit large quantities of SO ; in 1972, before pollution abatement
                                    A
equipment was installed, copper smelters emitted  an average of 6000 tons
of SO  per day, which is more than an order of magnitude larger than the
     /\
1975 S02 emissions from point sources in the Northern Great Plains (430
tons per day) and three times the projected 1986  SO  emissions (1990 tons
                                                   A
per day) in the Northern Great Plains.   Although  we have not developed a
regional model for the Southwest capable of handling the complex flow pat-
terns caused by rugged terrain, we examined the impact of the copper
smelter SO  emissions on visual range by locating hypothetical copper
          A
smelter emissions sources in the middle of the Northern Great Plains grid.
The hypothetical emission sources had characteristics identical  to the
copper smelters located in Arizona and New Mexico that were operating in
1972.

     We then ran the grid model for the meteorological conditions of the
Great Plains to evaluate the impact of the high SO  emission rates from
                                                  A
the copper smelters.  We summarize the results of this calculation for a
given time period in one of the test simulations  in Figures 61 through 63.
The state boundaries have been removed from these plots to emphasize that

-------
145





c»
*— «~



o
o.



o.





0.
CO



o.


o.
UJ




o.






o.
«*•



o.
OO





o_
C*J


o.




06 08 OL 09 OS Ofr 06 01 01

.... •' .- .-•••"-.. *..'"'.
..-• 	 - ? .', ,' •; \ •'..

'<•' '.'•'''
• •"' .' .' •'' ..'
" ' .' _ .' ..' ' ,, .-'" .. •• 	 	
: X" ."••'////>"., 	 •"'" / :
,.-'' • • f <••'' •' ' . '

•: ' i ••'•'/
.' .' / ; / 1 ''
'. . '' /' ..•>' .-' •'.' /'' !
.' .' / ? ,'' '
•' ••' ' t* ' •''
/,',•''
'"//''' '
-•"' •*' / •'* ' * r*"*****! •"" »
' * '•*"** "*"' ' ' WT '
; /*/.•"""" >/ / :
•l • •".*,•* .
.. *' .-••"* ."•'* .•• '' .*".*' '"' •'*
" \\T\'- 	 * -""!."•-• '''"..-'" '''-'? w^ .-' .-.--
--••"""""-*" ^ " • ' ' *fll';^ ''-f I • '"/' t»"T"'i"tt*'
*"....."" T •• " " .•''"<£' ,- ' " " ' j »fc5 .*' "*" "•• •'•'•' ' "5i»*' *

: "**••. •'--"' >/•'•' ••.'•>:-;;' ••-"' ;
' ' f'\^Lr'e t ' • ^"^ .'"•','
' *-' V '• «?*"••;•,:'' "' .-'"'
• " ••''.-'':' -.;.;:•• V '' .-,>'''
- " ' -"_•".' •"" ' •'! " •**' >^"'*
..... .... . .-•''_.,._ - ' ,;, %(•-'." ',.•' • ^ "
.. '" % '•''"' y.:'"- • ',."' '
,»•• '" . • ' ."/'..•"-'*" ,<•*' •' *". * -•' .•"'
* " - \V '' * '' ' ' "'"' ' fe .*" • ' ' •*'
" **-. (M :- •-'"!'*''.- ' . " .-*" t' *
'" ' . ' • .— --"*'" • '*' .* ' .'" •'
*'•-., * "' .-""" • '' • ' • *
"*'* ..,- • - * ,. '*\ '"•',''
,•-' ^'
. 	 	 	 .-'•'. v ..
*•?> .-"',-v .-•" ,'' . '''

. ' f --••" ' ,..-*'* >
/'^ . ^ . ' ' •''*

/-'* »

* ''
-.'_.'"
-
,...•''' ,-•-••• 	 " I 	 	 	 — .......
/ . ' " ..-• * "" "*'•. ..^
"^ ...-'" ..,. .•-•" "*•— • 	 / v
[ ^ ^ ..--•" ..,..•• * "'""- 	 	 .. 	 "•""
..-••'
(
"
- / ^
06 08 QL 09 OS 0> 06 OZ 01
~JU


..

o
•^



o
.0



.0
0)




.0
00



.0
r-

.0
— i
OO _J — 1
E  •— <
to z
O «3
III ; [ ^^
f n c/o ^t
LU sr 	 i
S> LU t— "
•a: ce
I O£ CX
rv LU  O
LU »— i O
LU r—
Q 3C
LU 1 — LU.
t— O O
CJ Q-
t— i >- (/)
C3 DC 2T
LU O
fV^ ~Z^ >-H
Q- O h-
__:
UD
LU
O£.
CD
I-H
U.

-------
146
06     08      Oi      09      OS
  Ob
oe
QZ     01




o
— '



o
0-



o_





o.
03



O.
^



0.
'
' / /' .-•'£"


-
* •' I*
/ / /' •'''''
/
' •'
{**
tfr
•'',"':
/
'" ' .' ,!
. P
*v
/
«' *x
''*.'"
.-"".•''•'••
"" 	 ••" " ,.••
-- -- 4 -•""" / N
" .- " • -.. .-' .''' *
•••-._. -
(t) •
/ .-*' • -

W .-•"'' ,•'•'*"''
.'* . '**' *'"
""""-. .* ' .••' .••'"' ,;
„•' ,..'•" .''


{
'.
.,••'
- ... ' ..--"" 'i
\ .'' ..-'*' f
.' -'* •'*' i

''
t"

' ^ W.''
.
-..•'"'
•
.
-
•
i ;

06 08 OL 09 OS Ok 06 OZ 01

r— fV)
x -^ Z
01 O
O f~*
co o o co
^y 1 1 1 121 y^*
O CO O i— i
t-i  co co
eC 00 MD
i D: i— i r^-
.0 GZ. rD sr CTI
vo ra o LU i —
o :c
•y C^ 1
i a: LU i— <
LU LU (— C£
LU O. _1 Q.
-O fV LU cf
"* 31 1— 21
1— Z CO U3
LU
_i c_> o: z
 1
*^^ <~^/ t^^ 1
1— Z LU O
0 •-< x; o
O ^D O r—
-2 UJ CO D.
°* oi co >- u_
Q_ et 3; O
.0 ^
LU
a:
rs
U-

-------
147
                               c;




(Zl




o
o.




o.
O)



o.
00


0.


o.
to


o_
in



o.
<**





o.
W>



o.
rg




O.






06 08 Oi 09 OS Ob 0£ 0? Ot

•'.-.'/:- .''"'VV' \X", 'r
•.<-'.', ! ••' .: ' '.• 'c0 r
• ^«! ,' .' . .' \ •*! ,1
. ' .' ' " ' ' • ' / •'
'• •'' •'& •'•'.-'" ...'" ,'"
• ,• . :'Q> •' •' •' .•'" I'

1 $/// '/// o
: "N •' • i .' iS.- .•' <""•
; /••''/ ••'!/' >^/ ""
/ / / i'" •'.•**.•'
.' . * / .• •' •
,• ' * ~ /f ••'
• '•/'/ *
. .- . .-' * ,-' i
,• .• / .' ' j -
.' *s •' f / > 1.
• ' -V / •' '' i
••' 'i^5 • / •' ••' L
". /:'*?/'! i I / ;_
; ^ (j . '...•',.••/ //// i;
..-••"' v '.-•*' •' ..•' -•' • V - !•
-•-.•-.::• - •-• '••-•.:".-" - • \"^r ..--, .-''.••'/ / f
* •:'":: l;;--:-"- ••- -• iX .-- •- "" ,'' /!»* '.
- 	 ...;—•--..-- «v / / _>v "- c5
>"""*... " 	 " % *'-.' ..'' / .-•"' 2
(5j * i *' * /* * ™
. , —,-* •- •*• '* •' . t' Cj J m

"n • . • ' •'' .' ' / •'' ^- (
: "" 	 V''"-''-''/ •••••-""" ^" ' :
***/•' •' i \ ••"'' t ' 1

'1 j' i *. '-• 	 X *•"

1 "•( \ '.' \* -•''

" ' • / / 1-0 . •' ,.-•''
^' i ,-' ••' •o* » .•' ' •*
>' .;' '' ,'4' i''
//'.'.•'
, '^i'-' •' /''
. ' '.^ . ,•'''
'''•''•'
'*•• . ''••''••<&> "

VV' -•' "*
"••' .'
.'
/*'"
^'
•
/
/
.-•''
..." /'"""' *
--•—'*"'' t'' \
.-.^— «*™***-""~" 3 30 '" *"'"" .*' .

06 08 Oi 09 OS Ot 06 OZ 01
-x ;c o
i— 2: Q- OO
< >- 2:
x a: z
o
o -fZ.0
 oo o
0 Q CO f—
.0 -^>
^4 ^—
O " U-
O UJ O
o: (—
C3 et OO
^ cc 2:
.0 0 0
O) ef 2: >— '
CQ 0 (—
<£ 1— O
2 ^
•o 2: o; o
•D __ O
s: u 	 i
oo uj o oo
OO I— •— i ^
•° ^ U- O <
^-Z3 o a.
E oo o;
^1 ° *"
.0 3 (— UJ
UJ UJ O UJ CC
CD 3C S C3
cC C£ Di 2t
a: uJ o cc
o U_ \ ' '
"10 i< i— oo ^
Z3 2* 2= CC
OO UJ O O
t— * C-> >— < 2T
> CC OO
0 UJ 00 UJ
•• 	 i ex i— -i re
< 2: H-
z: uo uj
o • zc
i — i O CC i — i
CD UJ
-O I i I  CC _J I^~
Q UJ CTi
Q -z. n »-
UJ cC 00
1__ |
r~~ —J
0 o E cc K-I
"AJ '""' -^ Lx* CC
" Q Q. a.
UJ O Q- ct
cc co o
O- r~ C_5 **O

.0
oo
to

UJ
CC
C3
t— •

-------
                                     148
this is a hypothetical test case.  We assumed a 0.5 percent per hour sul-
fate formation rate in these calculations  and negligible  primary  sulfate
emissions.   The results of a sensitivity analysis  using different sulfate
formation rates are summarized later in this  section  and  are  presented  in
detail  in Appendix G.

     Figure 61 shows that the maximum Sf^  concentrations  occur  at short
distances downwind of the hypothetical  smelters, which  are  located in the
center of the region.   However, as shown in Figure 62,  the  maximum S0|
                                   o                                 ^
concentrations (greater than 8 u9/m ) occur hundreds  of kilometers down-
wind of the smelters.   The impact of this  sulfate  on  visual  range is shown
in Figure 63.  The worst visibility (less  than 60  km) occurs  in one small
area in the upper middle portion of the region.  The  increased  sulfate
concentrations and resultant decreases in  visual range  occur  in two direc-
tions from the sources as a result of a change in  wind  direction that
occurred on the day before the simulation.  The calculated  concentration
maps for other time periods of this simulation period are presented in
Appendix G.

     The impact on visual range of assuming different sulfate formation
rates (0.3 and 1.0 percent per hour) is indicated  in  Figures  64 and 65.
Note that with the reduced sulfate formation the minimum  visual range is
70 km,  and with the increased sulfate formation rate  it is  40 km, which
compares with the minimum visual range of 60 km computed  for the base case
of 0.5 percent per hour.

     These sample calculations of reduced  visual range  cannot be compared
directly with the observational data from the Southwest because these cal-
culations were based on Northern Great Plains meteorological  conditions.
However, the results agree qualitatively with some of the conclusions of
the data analysis summarized in Chapter II:  namely,  SOX emissions from
copper smelters in the Southwest can cause a significant reduction in
visual  range even at locations several hundreds of kilometers downwind.
The predicted maximum SO? concentrations in these  simulations,  ranging from
            3
8 to 16 vig/m, agree qualitatively with measured maxima in  Arizona.  The

-------
149





o
-!'

o
o.
«-*




o.
at




o.
CD




o.
fw





o.
ID


0.
in



o.
«r





o.
Ol




o.
'' .*•-"' i'
•'. // *•*' /'' / o -
.-' / / / '•' m .
/ f '
/ /
; .• .• /
.'* -'* •' f
,' / / .'
.' ,.' •• f
1* .'' / •'' "
'„'*•"*
,' / / /
£, ••" ••' .'
$/ II \
.' /'* / ' "
'" ' •""*'• f^J f *
.-•'' 0^ •'* • ""• *'
.M***" * \ .. ' (X •' l&
-• - 	 — --•"".",-."•• • ""-••"'' ^ / >
'tfiljV-- . .. ,-•"*"" .•' /* /

' • ' OA ** 	 '* ' / /* * f*.
.-.. **"*•'•--.„., / .•' ^ f aC
?' '*. ***** /' /' .'' / *^ "
„ j J •'/'/• t .
/ ' / .- -•**' 1
''" " .'* / , ' •"' •*" / *
: 	 -•---•' ////" 1 •
'• ^ i& .•' / .*' / •
/ c> » ^0 ' ' •*' •
'. i "£ '""'* .-•''' "'S
.••'•.. O \
•, 9 }
• •*
' I f'' . '' "
"•"/•'.'
• / ' ^* •' .' •'*
.• ' .•' .-•*'

,••' .• V ••'"'
- , • ' / ' .'l^^
' ' '.''' "\
'•';''•''
:''.'' '.
p.-
-

f'
/
/
*•''
,.''&{•*.__ 	 . 	 ^- 	 .— '-••" .•••'"'\-
06 08 QL 09 OS Oft 06 02 01
E
I

X

o
-— *

a
.0
•••




.a
o>




o
ID




•g





.O
«


.O
U>



.O
*





.0
w>



,0




0
^




LU
CD
Z U-
«r zr o
c2 o
oo
_J Q Z
=3! LU O
^ 00 i— >
i— i CQ i— <
> 0
-2T
Q LU O
Z t— O 00
~™N —•«• ^^
~^ ^4^ ^—
O C£. 	 1 t— i
rv «3C eC
CD z: cj _i
:*£ o i— i a.
CJ i— i CD
<: I— O (—
CQ <=C _ J ef
2: 0 LU
=1 C£ Di Di
O O CD
CD U_ LU
'ZL i — z;
i — i iii 1 1_ i rv
^- i 	 5- iij
^^ P^ ac^ I-*-!
r> «=c n:
oo LI_ a; i —
co _i o cc:
=t rs u_ o
oo 2:
• oo
^--.a; 2: LU
E rs o a:

• — -ac oo
oo z
LU CcT ' — ' > — i
CD LU s;
z: a. LU UD
as H- CK: 01
«Z LU i—
_l LU (—

cj o re i—
i— l CO h- 1
a i— o o
LU Q- O
C£ U_ >- <^-
Q. O 3C r-

•
VO
LU
CD
HH
1 i

-------
                                   150



• -,
%-t _
— <



o
o.



O-
o>

0.
eo



O-





o.




0.




o.




o.



o.
'
'• '••"'''•.',•*? ' j "f

- .' '••'.' : •<£•' ''.' •""' .••' f
' t-' ^ • - "* ' C^ •-' * " *"
/ 'Cvatv" . ' ' ^^ ..-"'" Q

r ' -'*Y' :'. ''•"•', / /' •*
t- f\7 '. / -' " •' '* •'" t-
**• i -' ; •' .* " . •' L
• •• ':.£>• ..•'•>/,§> i-
•' ' • v' •''••'•' /"* t
''.''.•*•' i"
^, /••'•' /"V/ r
*/'"**' **V ,',' V

/••/.-•'.••"•'/ r
: :•;•••'•"•''/•$•.•'/.•' I
.- •'' " > 'C1 .- ' $*•• ' .' '* 'Qi i i
. ... "" 	 '"—'", ->- '1 ••'..*' -' ••/', "V '•— ^ i
"* '•" " 1)}" '•- • "" ' ' .. • '"' • ,• ' , t •' \
- '" 1" * •t?..".,'. •-•- 	 """ "' -' *'/'/ , ' a
' *'-- 	 crfi ., ^' •*••' .'' J A*' .••'"'.• Cf
' t?^ .. * " ". ^J^ •' / ' ' *1^ ,-•'' •* *"
* — . / / ,•' / / ^' ••* *v «'f f
} / • •' '• '••'',•''..-• ' -vl? /' f
	 •' .•' - - _. ,' .•' ..-•' t-' f
" -•' • ' • w* ' .-'*' -•'* ' . ' t
•* .•"'.'" • .'*' .' •'*' ' . • "'1 ••*' i-
"-••. .—• ,• .V r> •' • ,-'' _.""' ,; ,.' i.
- .''/.''•'•$? ''"" V' •'•'"' l
" • •'/'•' i • *. \ • t\y '*•
' • ,''*)'"'" * ""'*" *' .••' S '..
'.t \ \& '.:."""' /,;<•••' -
t *'""'. } • ' •'*' .'•''
') £"• '' '" •'.'"'
- .••'"" '\ I ^ ••' . .•'.*$••"'' \
: .' : .-' '  	 . 	 130 	 -, ».
iiiiiiiiiiiiiiil'ii'iiiiiiiii -*-'**f'* i I i i i i i t t i i i i i i.* i i i i i
E
O
X

o
. "~«
*^



o
.0



.0
•»

.0
QO



.0





.O
vD




.O
I/)




.O
«•



.O
en



.0



.0
w*




O <-i
UJ UJ o
CO T*
 QO
uj o
O CO «rf-
py ^f __
•^> DO
O U_
a: "o
e; uj
«r. §o
cc i— i
^ i 	
<; o 1-1
i— i r~i
=i<£o
— ^ CJ
I) O _l
co o z
<; uj i— i •— i
"«£ O -J
•^-Li 	 ID-
E-JO
NX "*"^ fV ^.^
	 CO UJ cj;
1 — UJ
UJ C£. UJ C£
2: o
•=t r: o: z
a: o en
(V 1 i 1 .J
• uj co

-------
                                    151
measured mean and maximum SOT concentrations in 1972 and 1973 in several
locations in Arizona are summarized in Table 5.  Note that mean  sulfate
                                           3
concentrations ranged from 2.2 to 12.5 ^g/m ,  and maxima ranged  from 5.8  to
41.0 yg/m3.
             TABLE 5.   MEAN  AND MAXIMUM  24-HOUR-AVERAGE
                       SULFATE  CONCENTRATIONS MEASURED
                       IN ARIZONA  IN  1972-1973
                                         [so]

                   _ Location        Mean     Maximum
                   Ajo              12.5      41.0
                   Douglas            9.1      25.9
                   Flagstaff          2.6        5.8
                   Grand Canyon       2.2        6.0
                   Phoenix            6.5      34.5
                   Superior          5.2      22.1
                   Tuba  City          2.6        9.7
                   Tucson            6.4      22.0
     The highest concentrations  occurred  in  the  immediate  vicinity of
smelters (e.g.,  Ajo,  Douglas,  and Superior)  and  in  cities  (e.g., Phoenix
and Tucson),  where, presumably,  the rate  of  sulfate formation would  increase
because of the elevated concentrations of reactive  species in  polluted
urban air.  The high sulfate concentrations  measured near  the  smelters  may
be the result of primary SOT emissions or the rapid conversion  to  sulfate
of emitted S02 in the initial  stages of plume dilution.  The measured
maximum sulfate concentrations in nonurban areas of Arizona distant  from
smelters (e.g., Flagstaff, Grand Canyon,  and Tuba City)  ranged  from  6  to
10 pg/m , in qualitative agreement with the  regional model calculations.

-------
                                   152
     Our approach to the calculation of atmospheric discoloration on the
regional scale has been to compute color parameters for particular loca-
tions (e.g., Class I areas) using the NOp and S07 concentrations obtained
using the regional model.  In these calculations, we assumed homogeneous
pollutant concentrations within the mixed layer, and we computed optical
effects for several different sight paths.  Exhibit 6 shows the output
from an example of these calculations for a location with background con-
                       3                    3
centrations of 3.4 ug/m  of sulfate, 30 yg/m  of coarse mode particulate,
and no NCL.  For different scattering angles 3 and sight path elevation
angles 6, the following specifications of color and color change (similar
to the parameters characterizing plume impact) are printed:

     >  Optical thickness (T).
     >  Light intensity (Y and L*).
     >  Chromaticity coordinates (x,y).
     >  Change in light intensity between the given background
        atmosphere and a Rayleigh (no particles) reference
        atmosphere for the given Q and 6  (AY,AL*)
     >  Contrast between the given background atmosphere and
        the reference at three wavelengths  [C(>K ^ = 0-40,
        0.55, and 0.70 ym].
     >  Blue-red ratio between given background and reference.
     >  Changes in chromaticity coordinates (AX,Ay).
     >  Color difference parameters [AE(L*l!*V*) and AE(L*a*b*)].

     With these parameters,  the color  of the background  sky at a given  loca-
tion in a region can be  specified  and  Munsell  color  notation can be deter-
mined from the values of L*,  x, and y.   The change  in  light intensity and
color between the given  location's sky and the reference atmosphere is  spe-
cified by contrast values AY, At*, AX, Ay, and A£.   These differences do
not have the same meaning as  the corresponding parameters for plume impact
because the observer compares the  light intensity and  coloration of the

-------
                                                                 153
i>:
m
a.
a
1



£ K

OH
 sS
  «
        £   s;
                                     ;r*T  l-c
             SSSSSSS
                                 > I- K * co w  •? N ; «• co a co
                                                               «• * s * ® I- *

                                                               N * aIt-1- * *
                                                                                                   «• i- co «• n *
                                                                                                  9 0* 4' ff1 s ft f-
                                                                                * « n tf»»« -   * »• n <

                                                                                ei — »ee t-(• i-   «c « — «»«• eo ec
         *>   *i •»• CO
         >   Sco-
         i
        i
               — rao — M—   N c* * cc co t» »   M * j *)« «r es
                                                 e - i- + 1-
                                                 — i- IT * fc
                                                                                  §« «*
                                    wwwN  S? * *>""£:§
                                                                          — »•
                                                                          n M
                                                                          flM
                                                               « ^ «. «. S' « -5'
                                                                                                 - «• n «cj - -
                                              9 !M M N * M -

                                CO CO CO CO CO CO  « (5 k' M M M N
                                                                              <-  «-*s-NCOt-
                                                                   ? co •• ep c* fr o  »p ff- r- w i^ * *
                                                                   > N N M — — —  ® M M C-t M f 1 IS
                                                                   !•«'««'»»«'  *"""""'
        ..   £jS®*S«<
                             C&QC^C&t^^^  *^^0>{v
                                                                  §»«*«* *   I- « — N N « rt   — * * w t> * *
                                                                  nowt^i^'c   oMft»n»o«ic   CO******
i  £
5  -

                                                   W 1- 1- » ES
                                                   Nf- *• r> * i
                                                   M 5' N «
                                                   ff SO C
                                              1- 0- M 5' N « 4
                                                         O CD
                                                                   05 1* «' N  « cc « ^ T:
                                                                                * N * — N *? l»
                                                                                «• N » «• «• + «
                                                                                - S 1- t- » ^6 -0
                                                                                   CM- 0- * M - l-
                                                                                      SR n c c> M M
                                                                                      Nme1-*^ —
                                                                                   * «• «• c- e- »• e-
        1

        5
»C9<>S*CfJ   ^•^h-M*®C-
np*«5*«r5   *«h-*«*-*
3rt^»«o*-«   (fc^ — c-*>*o^
>«K5^-*f *   — *•*
                                                                                                 1- * n N * * *
                                                                                                 e- *.**«!- 0»

                                                                                                 — » W O 8 N N
             *p fr- (6 *O Cj C5 *  i *
             99>O*9'C&9tM  CD*r

             SMMNNMS  S«

                                                   renncin  £^e
                                                                                * b- 9* 9 <» -•
                                                                                0» N «• S i 0
                                                                                                  D 04 JC C* W ^ C4
I       ^8:

g
        g
                                i    i  i  i  i    i  i  i  i   i  i  i    i  i  i  i  i i  i
                                                                 - * rt S M r-
                                                                i CO * ® « « «
                                                                                 i  i  t  i  t » i
                                                                                                    t  1  1  1  t  t
                                              *««**rt«  —mneoMMM
                                                                                    •* CO « C5 W
                             •» M — e-oCD*
                                                         — M  *9®K9COeO£'
                                                                                           ••51   CO^'C^NCOO'f
                                                                                             -   9- «> * * CO CO ft
                             row® N»»N
                                              — * 4 <> » M N

                                              CO N * J1 ?l S (5
                                                               t* o> * •• c- co co

                                                               CO N M CJ N C:l M
                                                                  cjSeo*-*  ^ ®
                                                                                                  fr CO *
                                                               N * n t» »• M —
                                                               <> *• *• i* •* i^ 10
                                                               »««** + •*
                                                               fl 0) 0) P» N N M
                                                                                »n9>ce4-s
                                                                                  §N N 9- CO N 1-
                                                                                  *>«•*"#•* *
                                                                                  M N M N N «
                                                                                                    p «• ce * i- n
                                              J P? »P ^ t^ *t CO



                                              J - ^ W ^ « I*

                                                                                                         -«!-
                                                                                                         * n co
                                                                                       05*Ne-
                                                                                »!>•«««»*
                                                                                                 * P5  N CO * «
                                                                                                 C* (*• *^ *^ ^ *^ ^



                                                                                                 ?SS!33c3«2

                                                                                                 •• w (* ft* t* w w
               Sn'I'^aNl-
               *««-—-
                                                6r5**«M»l-
                                                *«« — ••••
        &  .^,
        a     -c
                                                «««»
                                                - n + «
                                                         t^c*     ••CO**!*^     -^
                                                                                                                                 LU
                                                                                                                                 o;
                                                                                                                                    ««

                                                                                                                                    rs
                                                                                                                                    o
—I Q


LU
> LU

o o:


    o
I—
«=C u_
    o
oo
I—
o
                                                                                                                                U.
                                                                                                                                LU
                                                                                                                                    O
                                                                                                                                    CO
                                                                                                                                
-------
                                    154
plume and the background simultaneously;  a relatively sharp line of demarca-
tion separates the plume and the background.   For the homogeneous regional,
background atmosphere, the observer compares  the given atmosphere with  a
recollection of a clean atmosphere.  An exception would be an  observer  on
a mountain looking down on a homogeneous  mixed layer from a position where
he can compare the color of the mixed layer with the clean air above it.
These characteristics of the color differences for the homogeneous,
regional background atmosphere must be kept in mind when interpreting the
values of color difference parameters for determining the perceptibility
and the significance of atmospheric discoloration.  Further work is neces-
sary to identify the threshold values of the color difference  parameters
for the homogeneous atmosphere.

-------
                                   155
                 V    RECOMMENDATIONS  FOR FUTURE  WORK
     As stated in Chapter I, we have followed a  pragmatic  approach  to  the
development of models to predict anthropogenic visibility  impairment.   Our
goal has been to develop predictive tools helpful  in:

     >  Writing the report to Congress on visibility for setting
        policy and promulgating regulations.
     >  Evaluating the impact of proposed sources  and making siting
        and pollution control decisions.
     >  Determining the requirements for retrofitting pollution
        abatement equipment on existing sources.

This chapter recommends additional  work that we believe is necessary
in the near term to refine and test the models,  to assess  the impact of
proposed visibility regulations, to improve color  display  techniques,  to
develop a regional visibility model for the Southwest and  other  regions,
and to verify the predictions of the models by comparing them with  field
measurements.

     Figure 3 in Chapter I illustrates the potential uses  for visibility
models in environmental policy and  regulatory decisions, emission source
siting, and pollution control.  Assessment of the  extent of existing or
past visibility impairment can be accomplished through measurements using
such methods as (1) visual range and coloration  observation by trained
personnel, (2) photographic documentation of visual  range  and atmospheric
discoloration, (3) telephotometry,  (4) integrating nephelometry, and (5)
transmissometry.  However, estimation of the extent  of future impairment
(e.g., impairment caused by new sources or by the  abatement of existing
sources) requires a scientifically  based prediction  capability that can
provide estimates of visual  range and atmospheric  discoloration.

-------
                                  156
     Visibility modeling will  clearly play an important role in determining
a rational definition of "significant visibility impairment," in setting
environmental  policy (regulation promulgation, new source and existing
source retrofit reviews, and long-term goals), and in determining pollution
abatement and siting requirements on a case-by-case basis.   It is expected
that visibility impairment rather than ground-level air quality will  be-
come the dominant air quality issue and will  have a significant influence
on siting and pollution abatement decisions,  particularly in the West.

     The following sections outline the work  that we believe is necessary
to support the EPA's efforts in visibility regulation promulgation.   These
recommendations are presented in the order of their urgency.  In our view,
further testing of models and analysis of the impacts of visibility  regu-
lations should be done as soon as possible.

A.   IMPACT ANALYSIS IN SUPPORT OF REGULATION DEVELOPMENT

     The most urgent requirement for the application of visibility models
is the development of regulations.  Modeling  work will be necessary  to
determine siting constraints on new sources and requirements for pollution
abatement, both for new and existing sources, that will be imposed by pro-
posed visibility regulations.

     We have drawn two conclusions of major regulatory importance in our
initial applications of visibility models:

     >  The sulfate formed from S02 emitted from such sources as
        smelters and power plants may cause significantly reduced
        visual range at locations hundreds of kilometers away from
        the sources.  Indeed, the magnitude of the visibility im-
        pairment may increase with increasing distance downwind
        from the source, thereby making identification of cause
        and effect more difficult.

-------
                                  157
     >  NO  emissions from large coal-fired ppwer plants may cause
          X
        perceptible yellow-brown plumes and atmospheric discolora-
        tion more than 100 km downwind, particularly during stable
        atmospheric conditions.  Control of participate and S02
        emissions will make the discoloration more prominent by
        reducing the masking effect due to light scatter.

     The implications of these conclusions for siting and control are
obvious.  Impacts at large distances from emissions sources must be con-
sidered in siting studies.  Although the impact of power plant emissions
on visual range will be reduced by controlling SO  emissions, NO  control
                                                 x              x
is needed to reduce the yellow-brown discoloration that is caused by N0?.

     In the analysis of the impact of visibility on industry, considera-
tion must be given to:

     >  The magnitude and the spatial  and temporal extent of im-
        pairment for various sources,  ambient conditions, and
        geographical locations.
     >  The siting constraints imposed on new sources.
     >  The pollutants that must be controlled.
     >  The degree of control required to reduce visibility im-
        pairment to acceptable levels  compared with the capabi-
        lity for, feasibility of,  and  cost of implementation of
        various pollutant control  technologies.
     >  The appropriate regulatory policy to deal with visibi-
        lity impairment (i.e., emission standards, ambient air
        quality standards, or some standard of visual  range and
        atmospheric coloration).

B.   MODEL REFINEMENT AND TESTING

     Further work is recommended to test and refine the visibility models
in the near term, including:

-------
                                   158
     >  Further testing of the models through sensitivity analyses.
     >  Incorporation of more sophisticated gas-to-particle and
        aerosol growth algorithms in the code.
     >  Further assessment of the subjective visual  impact of and
        human threshold response to light intensity  and color changes.
     >  Refinement of color display.

     We limit our discussion here to work that should be done in the near
term to support the development of visibility regulations.  In the future,
when a complete set of measurements are available (e.g., from EPA's VISTTA
program), visibility models should be verified.   Measurements needed to
validate models include source emission rates, primary particulate size
distribution, meteorological conditions, plume dimensions, plume and ambi-
ent chemistry, aerosol size distribution and chemical composition, scat-
tering and absorption coefficients, solar direct and diffuse intensity, and
spectral light intensities and color photographs for several lines of sight,
Model validation is discussed in Section C.

1.    Model  Testing

     As we noted in Chapter IV and demonstrated  in Appendices E and G,  we
have started to test the models by applying them to  different emission  and
ambient conditions to test their sensitivity to  various input parameters,
including:

     >  Atmospheric stability (rate of dilution)
     >  Background ozone concentration
     >  Solar zenith angle
     >  Scattering angle
     >  Observer location and sight path orientation
     >  Background object light intensity and color
     >  Pollutant emission rate.

     We recommend that more sensitivity analyses be  performed with the
plume model for a variety of emission sources, meteorology, ambient

-------
                                   159
conditions, and viewing conditions to evaluate the model qualitatively.
The results of this sensitivity analysis could be displayed in graphical
and tabular form so that they could be used by environmental engineers in
regulatory actions, impact analyses, siting studies, and design.

     Further parametric analyses should be performed to evaluate the sen-
sitivity of model results to:

     >  Primary, secondary, and background aerosol size distribution.
     >  Ratio of diffuse to direct solar flux.
     >  Ratio of [NOg] to bscat-
     >  Locations of the background object and the plume relative
        to the observer.

     In a manner analogous to the ozone isopleth diagram, it may be
possible to characterize on an isopleth diagram the impact on visibility
of a range of combinations of the precursor pollutants.  By plotting
contours of constant value for some visibility-related objective function,
these precursor mixtures which lead to the same visibility conditions may
be identified.  Among the candidate objective functions are the contrast,
visual range, blue-red ratio, and AE.

      Another sort of visibility isopleth diagram might be constructed to
characterize general regional visibility.  Instead of HC and NO  as
                                                               /\
"precursors," sulfate and nitrogen dioxide could be viewed as "indices" of
visibility degradation.  By plotting concentrations of SCL and N0? along
the axes, one could determine isopleth lines that correspond to constant
objective function values.

     One of the chief values of the ozone isopleth diagram is that it
provides an easily computed estimate of the reduction in precursor emis-
sions from current ambient levels required to reach the NAAQS.   If the ob-
jective function chosen for use in the visibility isopleth diagrams were
the same as that employed in setting the federal standard, these diagrams

-------
                                   160
might have a similar use.  Required reductions in either SCL/NO  or SCL/NO?
                                                           C.   A      *T   t.
might be directly estimable.  If the development and use of visibility plots
were shown to be both feasible and reliable, they might prove to be impor-
tant tools as promulgation  and implementation of a federal visibility
standard occurs.  This could be of particular significance for state and
local agencies,  having limited resources and expertise, since they are re-
quired to incorporate visibility considerations in State  Implementation
Plans.

2.   6as-to-Partic1e Conversion and Aerosol Growth

     Currently in the visibility models gas-to-particle conversion (SOp to
SO^ and NO  to NO^) is treated in a simple manner through the use of pseudo-
  T*       X      O
first-order rate constants.  Secondary aerosol is assumed to form in the
accumulation mode with properties observed by Whitby and Sverdrup (1978),
in the Labadie plume.  Although this is a first approximation, it is a
reasonable assumption for modeling purposes.

     We recommend that further work be done to identify the reaction
mechanisms effecting the conversion of SOp and NO  to sulfates and nitrates
                                         t~       A
and typical concentrations of reactive species in various nonurban areas
(Class I) in the United  States.   Reactions  with  the following species  should
be  considered:
        OH'
           »
           >
           and 0^ (in clouds)
           I
        RO-
HO*
NH3
      Through  evaluation  of  the  concentrations  of  reactive  species  in  non-
urban areas and resultant formation rates, appropriate formation rates can
be selected by the user or computed in the code.

-------
                                  161
     We recommend that an aerosol growth model  be studied for possible
incorporation in the plume model.  Such a model would compute the equilib-
rium particle size distribution as sulfate and nitrate form and water con-
denses onto the particle surfaces.  We would determine if such a growth
model would improve the existing model sufficiently to justify its use.

3.   Assessment of Color Impact Thresholds

     We have incorporated into the visibility models the most recent
methods for quantifying color differences developed by the CIE in 1976
[AE(L*U*V*) and AE(L*a*b*)].  More work is necessary to determine what
standards for atmospheric coloration should be used (if any) in the vis-
ibility regulations.  The AE's appear to be reasonable parameters to
characterize color changes associated with pollution; however, more work
is needed to determine what AE values mean subjectively in various cases
and what perceptibility-threshold and acceptability-threshold values should
be adopted in the analysis of atmospheric discoloration.

4.   Refinement ofColor Display

     In few instances is the display of model results so important as it
is in the prediction of visibility impact.  A considerable number of sep-
arate lists of information are required in order to characterize a single
scene.  However, the human eye and brain together are able to assemble and
integrate all this input, synthesizing it to a final impression of visual
impairment.  It is the subjective judgments based on these impressions
that constitute "visual impact" of the most fundamental sort.

     Consequently, the practical utility of a model depends on its ability
to collapse  its predictions into a similarly simple and usable format.
It is for this reason that model predictions in this study have been ex-
pressed not only by means of specific visibility-related parameters, but
also through artist renderings of entire scenes with colors and intensi-
ties of sky and pollutant determined by model predictions.

-------
                                 162
     Several advantages have been achieved as a result.   Predictions can
be assimilated more easily.  Judgments about visual  impairment are faci-
litated.  The visibility impact projected to result  from construction or
alteration of a facility can be more readily presented to and evaluated
by policy-makers and the general public.

     While considerable progress has been made in this study to develop
suitable means for displaying model  predictions, the following continued
efforts seem to hold the promise of substantial payoff:

     >  Additional studies could be conducted of the feasibility of
        using artist-produced color illustrations to represent
        visibility model predictions.
     >  A study could be performed of the feasibility of using
        artist renderings of plume and atmospheric coloration pre-
        dictions "overlayed" onto actual photographs of terrain.
        This "photo-montage" technique has been used successfully
        by the U.S. Forest Service's MOSAIC land use assessment
        program.
     >  A study could be undertaken of the comparative accuracy
        and acceptability of each of the above two display tech-
        niques, as well as with the color video approach used by
        workers at Los Alamos.
     >  The Perspective Terrain Viewing Program (PTVP) could be
        linked to the plume visibility prediction model  (PLUVUE).
        By doing so, one could first display the terrain as seen
        from a specified location, select a point whose colora-
        tion was desired (as expressed in chromaticity coordinates,
        perhaps), and calculate directly the visibility predicted
        at that point.  In this way, use of the visibility model
        would be much more tightly integrated conceptually with
        terrain views.

-------
                                   163
C.   MODEL VALIDATION

     In this section we discuss our preliminary thoughts on a model  vali-
dation effort, including:

     >  The type of measurement program that is needed.
     >  The specific measurements that should be made.
     >  The type of analysis of measurements and model  pre-
        dictions needed to assess model performance and to
        provide direction for model refinement.

1.   The Type of Measurement Program

     No attempt should be made to validate SAI's regional  visibility model
at this time.   Rather, efforts should be aimed at providing a comprehen-
sive set of measurements downwind of a point source so  that the plume vis-
ibility model  can be validated.  Information obtained from the point source
measurement program will be useful later in regional model validation and
refinement.

     A large, coal-fired power plant should be selected for the measurement
program.  The visibility regulations required by the Clean Air Act Amend-
ments of 1977 are likely to affect power plants, particularly in the wes-
tern United States, more than any other single class of emissions source.
Although copper smelters emit large quantities of SO ,  which has been shown
                                                    A
to significantly affect visual range in the Southwest,  most of those sources
are exempted from the requirements of Section 169A on visibility protection
because they are more than 15 years old.

     The power plant that is selected for measurement should have the fol-
lowing attributes:

     >  Pollutant emissions should be easily measurable and
        should be relatively constant during the measurement
        program.

-------
                                  164
     >  Participate emissions  should  be  well  controlled  using
        state-of-the-art abatement  equipment, such  as  efficient
        electrostatic precipitators or wet scrubbers,  so the
        plant is representative of  modern  coal-fired power  plants.
        A major objective of the measurement  program is  not to
        measure the visibility impairment  caused  by large emission
        rates of primary particulates from older  plants, but to
        assess the visibility  impairment caused by  secondary aero-
        sols (i.e., sulfates and nitrates) and NCL.  Large  emission
        rates of primary particulate  might interfere with the mea-
        surement of secondary  aerosol generation  and light  scattering.
     >  Sulfur dioxide (SO^) emissions should not be controlled  by
        scrubbers so that a significant  amount of SC^  is available
        for conversion to sulfate.
     >  The power plant should be located  in  the  western United
        States and should be isolated so that the plume  can easily
        be identified, tracked, and measured  without interference
        from plumes from other sources.

     The emphasis of the measurement  program  should be on the visibility
impairment caused at far downwind distances.   This  contrasts with the
objectives of most air quality monitoring  programs, which are designed  to
determine the maximum ground-level  pollutant  concentrations, which  gener-
ally occur within 20 to 30 km of the  source.   Visibility impairment  appears
to be a long-range air pollution problem because  it is caused by secondary
pollutants (NOp, sulfates, and nitrates) that are formed relatively  slowly
in the atmosphere.  Preliminary calculations  show that the  maximum  reduc-
tions in visual range occur hundreds  of  kilometers  from  power plants and
maximum plume discoloration due to NO^ occurs during stable conditions  40
to 100 km downwind.  Visibility impairment at distances  100 km or more
downwind of proposed or existing emissions sources  will  be  the controlling
factor in determining the amount of pollution control  equipment  that must
be retrofitted on existing sources and in  evaluating what the siting and

-------
                                   165
emission constraints on new sources will be.   Therefore, long-range impacts
must be measured so that the visibility model can be validated.

     A crucial part of the long-range tracking and measurement of plume
visibility impairment will be the measurement of upper air transport winds
at frequent intervals and several locations so that accurate, real-time
plume trajectories can be calculated.  These trajectories will  be needed
to help track the plume and to identify the plume location relative to
fixed observation locations.   Also, the upper air wind data can  be used
later in conjunction with National Weather Service measurements  to calcu-
late back trajectories and air parcel histories, so that potential sources
of background aerosol and trace gases can be identified.  For example,
during a measurement program at a point source in a nonurban area of the
Southwest, there might be several days when air originating from an urban
area or from a copper smelter complex would get transported to  the measure-
ment area.  One could thus, with little additional expenditure,  supplement
the information regarding point-source plume impact with information
regarding the regional impact of distant sources.

     An attempt should be made to measure plume visibility impairment dur-
ing stable meteorological conditions.  Greatest visibility impairment,
according to model calculations, occurs during stable conditions (e.g.,
Pasquill E or F).   However, even greater impacts might occur during stag-
nant conditions or in locations where there are flow reversals  (e.g.,
drainage flows) that could cause a build-up of pollutants in a  confined
area.   A study of climatological records could be carried out prior to
the measurement program so that periods of the year most likely  to have
stable or stagnant conditions could be selected.  For example,  in the
Southwest stable conditions occur most frequently in the winter.

2.   Specific Measurements

     A large number of measurements will be required to validate the plume
visibility model.   The necessity of each measurement can be appreciated
by examining Figure 13 (Chapter III), which shows the schematic  logic flow

-------
                                    166
diagram of the visibility models.   Most air quality measurement  programs
and models are concerned only with the first two elements  of the visibility
model—the emissions and the atmospheric transport, diffusion, and removal
processes.  The desired measurements and output are time-averaged pollutant
concentrations at given ground-level locations.   However,  in the visibility
model and in measurements to validate visibility models,  the desired result
is a light intensity, perceived by an observer at a given  ground-level
location, which is affected by air pollutants some distance away from the
observer.

     Thus, the most important single measurement necessary for the valida-
tion of visibility models is of the spectral light intensity I(A) for spe-
cific observer locations and lines of sight.  The spectral light intensity,
a strictly physical parameter, can be translated to visibility-related
psychophysical parameters, such as luminance (Y), chromaticity  (x, y),
contrast (C), and the color difference parameter (A£), by  weighting the
light intensity by the spectral response characteristics  of the  three
different light sensors of the human eye.  These psychophysical  parameters
are directly related to what an observer sees and are necessary  and suffi-
cient for quantitying visual range and atmospheric discoloration.  The
multiwavelength telephotometer is the only instrument with which we are
familiar that can directly measure these psychophysical parameters.  By
equipping the instrument with color filters corresponding to the spectral
response of the three light receptors of the human eye, one can  measure
tristimulus values (X, Y, and Z) for a given line of sight and  calculate
Y, x, y, C, and A£.  The telephotometer can also be used to determine
visual range by measuring the contrast between a distant mountain and
the horizon sky.  Since the light intensity of several lines of  sight can
be measured with a single telephotometer at one location,  three  or four
ground-based telephotometer measurement stations might be sufficient for
a measurement program at a single point source.  Station locations might
be in a preferred transport direction (in stable conditions) at  distances
from the source of 20, 50, 100, and 150 km.  If possible, some  of these

-------
                                   167
stations might be at vista points in Class I areas.   Telephotometer sta-
tions can be moved fairly easily, depending on the transport of the plume,
to the most strategic locations and could be located on high terrain where
views in many directions are possible.   It would be valuable to have sta-
tions on opposite  sides  of a plume so that the same sight path could be
sampled from different angles to study the effect of the scattering angle e.
One telephotometer could be constantly moved to obtain views of the plume
from several angles and distances to characterize fully the effects of
plume-observer geometry.   For example,  measurements of the plume could be
made at several locations along a road or highway to evaluate the effect
of the plume-observer distance and the angles between the line of sight
and the plume centerline and between the line of sight and the horizon.

     Each telephotometer operator should take color photographs of the
scenes that he is measuring with the telephotometer for later documentation
of contrast, atmospheric coloration, and the positions of the plume and the
sampling aircraft.   At the edge of the camera's field of view in each photo-
graph, a color test strip should be placed (in direct sunlight, if possible)
so that the quality of the development of the color film can be controlled
and checked.  In cases of forward scatter (e < 90°)  where the sun is in
front of the camera, the color test strip cannot be placed both in the field
of view and in direct sunlight.   In such cases, the test strip can be photo-
graphed separately at some interval.  It may be possible to maintain and
check color film development quality by calibration using the color test
strip only once per role of film.  The feasibility of cross-checking the
color photographs with the multiwavelength telephotometer measurements
should be evaluated.  Color time-lapse movies from strategic vista points
could also be taken.

     To link the measured spectral  intensity to air pollution, one must
know the aerosol and NOp concentrations along the specific sight paths.
Thus, airborne measurements of NOp concentration, scattering coefficient
(b   ,), and aerosol size distribution will be necessary.   Attempts should

-------
                                   168
be made to make aircraft traverses of the plume as  close  to  the  lines  of
sight used in the telephotometer measurements as possible.   It  is  essen-
tial to measure the location of the plume relative  to  telephotometer
stations since coloration will  depend on the proximity of the plume  to
the telephotometer.  Airborne measurements could be supplemented and
checked with correlation spectrometer measurements  of  N0? burden.  Since
the plume optical depth due to NCL is directly proportional  to  the N0~
burden, this measurement would be valuable.   The correlation spectro-
iiieter should be considered as an optional supplement to airborne
monitoring.

     Direct and diffuse solar flux should be measured  using  a pyrheliometer/
pyranometer combination.  The occurrence of cloud cover should  be  docu-
mented.  The location of the sun should either be measured or calculated
so that the solar zenith angle and the scattering angle for  all  telephoto-
meter and photographic lines of sight can be calculated later.   Alterna-
tively, scattering angles could be measured at the  time of measurement.
It is imperative that the line of sight of each light  intensity measure-
ment be specified and recorded; measurements of the scattering  angle,
solar zenith angle, sight path azimuth, sight path  elevation angle,
observer location, plume location, and plume dimensions fully describe
each line of sight.

     An important part of the measurement program should  be  the determi-
nation of the production site, chemical composition, size distribution,
and causes of secondary aerosol production, particularly  at  large  down-
wind distances.  The secondary aerosol production rate could be determined
by calculating [SO=]/[S02], [NO^/LNO^, [bscat]/[S02], and  [bscat]/[NOx].
Each of these ratios will increase with secondary aerosol formation.  The
measured aerosol size distribution, chemical composition, mass  concentra-
tion, and scattering coefficient should be cross-checked  using  Mie theory
and accounting for the cations and liquid water associated with sulfates
and nitrates.  Hypotheses regarding the mechanisms  of  secondary aerosol
formation should be tested by looking at the time-dependent  rate of

-------
                                    169
aerosol formation.  If possible, measurements of background and plume
ammonia and radical concentrations should be made to identify possible
fundamental reactions effecting gas-to-particle conversion.  Some attempt
should be made to measure the refractive indices, including the imaginary
(absorption) components, of the background, fly ash, and secondary aerosols.

     The conversion of NO to NCL in the plume should be measured.  Ozone
concentrations in the background air and in the plume and ultraviolet radi-
ation should be measured to test the validity of the steady-state assump-
tion used in calculating plume N02 production.

     Plume dispersion parameters (a , o2) should be calculated from the
measurements of peak plume concentrations.   The wind field at the plume
centerline should be measured by pibal  releases from several locations at
hourly or three-hourly intervals.  The plume position and transit times
based on measured wind speed and direction  at plume height should be com-
puted on a real-time basis and should be compared with actual plume position.
Real-time calculations of plume position in the field would be used by the
pilot and ground-level observers to determine the location of the plume,
and to direct the airborne plume measurements at night and at far down-
wind distances.  These calculations could also be used in conjunction with
weather forecasts to relocate ground-based  stations to optimize plume
impact measurement.  Vertical temperature gradients should be measured
during the aircraft flights.

     Finally, the emissions from the power  plant must be measured accur-
ately.  If possible, the following measurements should be made throughout
the measurement program:  mass emission rates or flue gas concentrations
of S02, NO, N02» and fly ash, in-stack opacity, flue gas volumetric flow
rate, flue gas temperature, and flue gas oxygen concentration.  It would
be desirable in simplifying the measurement program if the power plant
operated at constant capacity throughout the measurement program.

-------
                                   170
3.   Data Analysis, Assessment of Model  Performance,  and Model  Refinement

     Data collected during the measurement program must be reduced  and  com-
piled in a format useful  for providing input data for the visibility computer
simulation models.   After the plume visibility model  is run,  the calculated
SC>2> NO, N02, 0^, SO^, and NO"  concentrations, scattering coefficients,
spectral light intensities, and visual effects (reduction in  visual  range,
plume perceptibility, and atmospheric discoloration)  should be  compared with
measurements.

     Model calculations should be made based on the measured  values of:

     >  Emission rates
     >  Upper air wind speed and direction
     >  Plume dilution (a , a )
     >  Secondary aerosol formation rates
     >  Aerosol size distributions
     >  Ambient conditions
     >  Geometry of sun,  plume, and observer.

     Calculations and measurements of the following parameters  could be
compared:

     >  Pollutant concentrations
     >  [N02]/[NOX]
     >  bscat
     >  bscat/mass ratios
     >  Visual range
     >  Luminance (Y)
     >  Chromaticity (x,  y)
     >  Perceptibility (A£)
     >  Contrast.

-------
                                     171
In addition, SAI's plume perspective and color display techniques could be
used to create color renderings of certain vistas for comparison with color
photographs.

     In comparing model calculations and measurements necessary for model
validation it is important to consider the errors that can occur in:

     >  Measurement of input parameters
     >  Measurement of output parameters
     >  Model formulation.

     Since we want to test and validate the model formulation, it is essen-
tial that errors in measurement of input and output data be minimized, error
bounds established, and that all  parameters necessary for defining model
input and output be measured.

     Model performance can be evaluated using:

     >  Correlation coefficients.
     >  Differences between measured and calculated values:  Either
        mean or root-mean-square,  and either absolute or relative
        differences.
     >  Ratio of measured to calculated values.
     >  Regression statistics.
     >  Qualitative comparisons.

     A thorough model evaluation may identify directions for model  refinement.
Limits on model applicability and  accuracy may also be established.  After
further model refinement and development based on the information gained  from
the comparison with measurements,  it could be advantageous to test the model
again using another set of measurements, possibly from another emissions
source, and allowing  no intermediate fine tuning of the model  input parameters,

-------
                                    172
D.   FURTHER DATA ANALYSIS

     We have obtained an extensive data base with which further analyses
of anthropogenic visibility impairment can be made, including:

     >  Nearly 500 station-years of National Weather Service (NWS)
        visibility and meteorological data.
     >  About 10 station-years of National Park Service visibility
        data.
     >  Holzworth mixing depth and mixed layer wind speed for all NWS
        upper air stations in the United States for 1960 through 1964.

     We recommend that further data analysis be coupled with the develop-
ment of a regional visibility model for the Southwest.  The objectives of
this analysis would be to determine through an analysis of upper air flow
trajectories typical transport wind fields which could be used for re-
gional calculations.  Temporal and spatial variations in visual range
could be studied in conjunction with calculated trajectories to determine
the transport of emissions from source areas to clean nonurban areas (for
example, southern Utah).  Also, inferences could be made as to the rate of
sulfate formation and removal by studying trajectories, ground-level sul-
fate measurments, and visual range observations.

     In this report, visual range has been shown to be correlated with
many variables.  Correlations with meteorological variables as well as
diurnal and  seasonal variations have been explored.  However, these rela-
tionships have been studied one variable at a time, and no attempts have
been made to elucidate the simultaneous effects of many variables.  In
statistical  terms, only univariate analyses have been made thus far,
though multivariate analyses are needed.

     A question of great interest is what combinations of meteorological
conditions are associated with poor visibility?  This question could be
investigated using a multivariate classification technique, such as linear

-------
                                   173
discriminant analysis  [e.g., Gnanadesikan (1977), Morrison (1976)], which is
a method that assigns multivariate observations to one of several classes.
This is done by finding planes in the multidimensional space of the inde-
pendent variables (in this case, the meteorological variables) that opti-
mally divide the observations (visual ranges) into different classes (e.g.,
visual range between 80 and 100 km).  Discriminant functions for subsets
of the data can be determined, for example,  for different years or for the
period of the copper strike.  Differences between discriminant functions
would indicate that the conditions associated with various visual ranges
were changing.  Misclassification rates should be evaluated for each dis-
criminant function to indicate its utility as a predictor.

     Another technique that could be applied to the data set to elucidate
the dependence of visual range on other variables is multiple regression.
However, since many of the independent variables that would be used in the
regression (e.g., the meteorological variables) are likely to be highly
correlated, some dimensionality-reducing method, such as factor analysis,
should be applied to these variables first.   In this way, some smaller
number of uncorrelated surrogates could be generated, and the multiple re-
gression could be made more meaningful and useful.  Alternatively, a vari-
able selection method such as Cp analysis (Daniel and Wood, 1971) could be
used in conjunction with the regression.

     Intervention analysis can be applied to determine whether a sudden
shift in conditions was associated with a corresponding change in visual
range (Box and Tiao, 1965, 1975).  This technique would be applicable
to quantifying the changes in visual range that may have occurred during
the copper strikes.   This time series method allows for the nonindependence
of successive observations in evaluating a change in level of a series of
observations.  (A t-test of the difference in levels before and after the
event would be invalid because of the dependence between successive ob-
servations.)  The analysis proceeds by calculating a function of the ob-
servations, with a known statistical distribution, which estimates the
shift in level.   Straightforward statistical inference then gives the

-------
                                  174
level  of significance of the observed shift.   Application  of time  series
techniques should enable both an analysis of  trends in visual  range  and
sudden shifts due to events such as  the copper strike.

E.   DEVELOPMENT OF A SOUTHWEST REGIONAL VISIBILITY MODEL

     For several reasons, the Southwest is likely to be the first  region
in which visibility regulations, which are to be promulgated by August
1979,  are implemented.   First, there are a large number of mandatory
federal Class I areas in the Southwest, including national  parks of  such
obvious scenic value as the Grand Canyon, Bryce Canyon, Canyonlands, and
Arches.  Second, the existing visual range in clean areas  of the Southwest
is probably the best of anywhere in  the contiguous United  States.  Accord-
ing to our analysis of visibility data (see Appendix A), there are several
locations in the Southwest, notably  in northern Arizona, Utah, Colorado,
and New Mexico, where visual range is often greater than 160 km (100 miles).
Indeed, based on nephelometer measurements in Bryce Canyon reported  by
Charlson (private communication, 1978), visual range at times may  approach
the Rayleigh scattering limit of 390 km (240  miles) in the Southwest.
Third, significant energy development is planned for the Southwest,  par-
ticularly in Utah and Colorado.  Several large coal-fired  power plants
are currently being proposed to be located at sites in the Southwest, in-
cluding Harry Allen (2000 Mwe), Intermountain Power Project (3000  Mwe),
Warner Valley (500 Mwe), and Garfield (2000 Mwe).  Fourth, several large
coal-fired power plants are currently in operation in the  Southwest, some
of whose plumes have been observed from scenic vistas in national  parks
such as Bryce Canyon and Mesa Verde.  These plants include Four Corners
(2175 Mwe), Mohave (1500 Mwe),  Huntington Canyon (800 Mwe), Navajo  (2300
Mwe),  and San Juan (1500 Mwe).  Finally, several very large emissions sources
are located in the Southwest or are  in the prevailing upwind direction from
the Southwest.  These sources include the copper smelters, whose current
aggregate SO  emissions are more than 3000 tons per day, and the metropolitan
            /\
areas  of Phoenix, Tucson, Las Vegas, Salt Lake City, and Los Angeles, from
which pollution may be transported to Southwest mandatory  Class I  areas.

-------
                                   175
     Since spectacular scenery in the Southwest is enhanced by generally
excellent visibility and since considerable development of coal resources
is planned or has already occurred, a regional visibility model that can
study and answer the following questions is needed:

     >  Will a proposed power plant have an impact on visual range
        in mandatory Class I areas located 100, 200, 500, or even
        1000 km away?  Will yellow-brown haze be visible?  What sit-
        ing alternatives exist, and how much pollution abatement is
        required?
     >  Does an existing power plant's plume have a significant im-
        pact on visual range and atmospheric color in national
        parks?  Where?  How much?  How often?  What pollution
        abatement equipment is required (i.e., particulate, SOX,
        or NOX control)?
     >  Does the existing copper smelter complex have to control
        SO  emissions further to reduce visibility impairment?
          A
        Where does SO  get transported, how much is removed by
                     A.
        natural atmospheric processes, and how much is converted
        to sulfates?
     >  Are sulfate, nitrate, and organic aerosol*, emitted from
        urban areas, such as Phoenix, Salt Lake City, or even Los
        Angeles, transported to mandatory Class I areas in the
        Southwest?  Do they have a significant impact on visibility?

These questions have potentially significant technical, socioeconomic, and
political  implications.   For example, if anthropogenic pollution is found
to be the cause of significant visibility impairment in the Grand Canyon,
the question to be answered is which combinations of sources contribute--
urban areas, the copper  smelters, or a nearby coal-fired power plant?
A Southwest regional visibility model should be developed to point toward
the answers to these questions and to provide guidance for critical decisions.

-------
                                   176
                              REFERENCES
Alkezweeny, A.  J.,  and D.  C.  Powell  (1977),  "Estimation  of Transformation
     Rate of S02 to $04 from Atmospheric  Concentration Data," Atmos.
     Environ..  Vol. 11, pp.  179-182.

American Society for Testing and Materials  (1974),  "Standard Method of
     Specifying Color by the Munsell  System,"  Dl535-68,  Philadelphia,
     Pennsylvania.

Arizona Department of Health Services (1977),  "First  Annual Report on
     Arizona Copper Smelter  Pollution Control  Technology, Phoenix,
     Arizona.

Atkinson, R., R. A. Perry, and J.  N.  Pitts,  Jr.  (1976),  "Rate Constants
     for the Reactions of the OH Radical  with  N02  (M  = Ar and Ne) and
     S02 (M = Ar)," J. Chem.  Phys.,  Vol.  65, pp. 306-310.

Barrie, L., and H.  W. Georgii (1976), "An Experimental Investigation of
     the Absorption of Sulfur Dioxide by  Water Drops  Containing  Heavy
     Metal Ions," Atmos. Environ.. Vol.  10,  pp.  743-749.

Bassett, H., and W. G. Parker (1951), "The  Oxidation  of  Sulfurous Acid,"
     J. Chem. Soc.. Pt. 2, pp. 1540-1560.

Bauer, E. (1973), "Dispersion of Tracers  in the Atmosphere:  Survey of
     Meteorological Data," Paper P-925,  Institute  of  Defense Analysis,
     Arlington, Virginia.

Baulch, D. L.,  D. D. Drysdale, and D. G.  Home (1973), Evaluated Kinetic
     Data for High Temperature Reactions. Volume 2--Homogeneous  Gas
     Phase Reactions of the  Hg-^-O;? System (CRC Press.  Cleveland, Ohio).

Beilke, S., and G.  Gravenhorst (1977), "Heterogeneous S02 Oxidation in
     the Droplet Phase," International Symposium on Sulfur  in the
     Atmosphere, Dubrovnik,  Yugoslavia.

Beilke, S., D.  Lamb, and J.  Mueller (1975), "On the Uncatalyzed  Oxida-
     tion of Atmospheric S02 by Oxygen in Aqueous  Systems," Atmos.
     Environ..  Vol. 9, pp. 1083-1090.

Benarie, M., A. Nonat, and T. Menard (1973),  "Etude de la Transformation
     de L'Anhydride Sulfureaux en Acide Sulfurique en Relation avec les
     Donnees Climatologiques, dans un Ensembly Urbain in a  Caractere
     Industriel, Rouen," Atmos. Environ.. Vol. 7,  pp. 403-421.

-------
                                  177
Benson, S. W. (1968), Thermgcheniical  Kinetics (John Wiley & Sons,  New
     York, New York).

Bergstrom, R. W.  (1973), "Extinction  and Absorption Coefficients of  the
     Atmospheric  Aerosol as a Function of Particle Size," Beitra'ge Zur
     Physik der Atmosphare, Vol.  46,  pp. 223-234.

Bergstrom, R. W., and J. T. Peterson  (1977),  "Comparison  of Predicted
     and Observed Solar Radiation in  an Urban Area," J. Appl.  Meteor.,
     Vol.  16, pp. 1107-1116.

Bergstrom, R. W., and R. Viskanta (1974), "Spherical Harmonics Approxima-
     tion  for Radiative Transfer  in Polluted  Atmospheres,"  Progress  in
     Astronautics and Aeronautics,  Vol. 35, pp.  23-40 (MIT  Press,
     Cambridge,  Massachusetts).

Boris,  J.  P., and D.  L. Book (1973),  "Flux-Corrected Transport--!:  SHASTA
     A fluid Transport Algorithm  That Works," J   Computational  Phys.,
     Vol.  11, pp. 38-69.

Box, G.E.P., and  G.  C. Tiao (1975), "Intervention  Analysis  with Applica-
     tions to Economic and Environmental Problems, J. Amer.  Stat.  Assoc.,
     Vol.  70, p.  70.

           (1965),  "A Change in Level  of a Non-stationary Time Series,"
     Biometrika,  Vol.  52,  Nos.  1  and 2,  p.  181.

Briggs, G. A.  (1969),  "Plume Rise,"  Office  of Information  Services,  U.S.
     Atomic Energy Commission,  Washington,  D.C.  (National  Technical
     Information Service TID-25075).

Brimblecomb, P.,  and D.  J. Spedding  (1974), "The Catalytic Oxidation of
     Micromolar Aqueous  SOg--!.  Oxidation  in Dilute Solutions  Containing
     Iron (III)," Atmos. Environ., Vol.  8,  pp.  937-945.

Businger, J. A.,  et al.  (1971), "Flux-Profile Relationships in  the
     Atmospheric Surface Layer,"  J.  Atmos.  Sci., Vol.  28,  pp. 181-189.

Calvert, J. G., et al.  (1978),  "Mechanism of the Homogeneous Oxidation
     of Sulfur Dioxide in the Troposphere," Atmos.  Environ., Vol. 12
     (in press).

           (1977), "Mechanism of  the Homogeneous Oxidation of Sulfur
     Dioxide in the Troposphere,"  International  Symposium on  Sulfur
     in the Atmosphere,  7-14 September 1977,  Dubrovnik,  Yugoslavia.

Cass, G. R. (1976), "The Relationship Between Sulfate Air Quality and
     Visibility at Los Angelas,"  EQL Memorandum No.  18,  California
     Institute of Technology, Pasadena, California.

Chamberlain, A. C. (1966),  "Transport of Gases to and from Grass  and
     Grass-like Surfaces,"  Proc.  Roy. Soc..  Vol.  A290,  pp.  236-260.

-------
                                   178
Charlson, R. J., and N. C. Ahlquist (1969), "Brown Haze:  N02 or
     Aerosol?," Atmos. Environ., Vol.  3, pp. 653-656.

Charlson, R. J., N. C. Ahlquist, and H.  Horvath (1968),  Atmos.  Environ.,
     Vol. 2, p. 455.

Chen, T., and C. H. Barren (1972),  "Some Aspects  of the  Homogenous
     Kinetics of Sulfite Oxidation," Ind.  Eng.  Chem.  Fund.,  Vol.  11,
     pp. 446-470.

Cheng, R. T., M. Corn, and J.  I. Frohliger (1971), "Contribution  to the
     Reaction Kinetics of Water Soluble  Aerosols  and SO? in  Air at  ppm
     Concentrations," Atmos.  Environ.,  Vol. 5,  pp. 987-1008.

Committee on Colorimetry, Optical  Society  of America (1963),  "The Science
     of Color," Washington, D.C.

Conner, W. D.,  and J. R. Hodkinson (1972), "Optical  Properties  and  Visual
     Effects of Smoke-stack Plumes," AP-30, Office of Air Programs,
     Environmental Protection Agency,  Research  Triangle  Park, North
     Carolina.

Covert, D. S.,  R. J. Charlson, and N.  C. Ahlquist (1972), "A Study  of
     the Relationship of Chemical  Composition and Humidity to Light
     Scattering by Aerosols,"  J. Appl.  Meteor., Vol.  11, pp.  968-976.

Cox, R. A.,  and S. A. Penkett (1972),  "Aersol Formation  from Sulphur
     Dioxide in the Presence of Ozone  and  Olefinic Hydrocarbons," J.  Chem.
     Soc., Vol. 68, p. 1735.

           (1971a), "Photo-Oxidation of Atmospheric S02>" Nature. Vol.  229,
     pp. 486-487.
           (1971b), "Oxidation of Atmospheric S02 by Products  of the Ozone-
     Olefin Reaction," Nature,  Vol.  230, pp.  321-322.

	 (1970), "The Photo-Oxidation of Sulphur Dioxide in Sunlight,"
     Atmos. Environ., Vol.  4, p.  425.

Crutzen, P. J., and J. Fishman  (1977),  "Average Concentration of OH in
     the Northern Hemisphere Troposphere, and the Budgets  of CH., CO,
     and HC," Geophys. Res.  Letters, in press.

Daniel, C., and F. S. Wood (1971),  Fitting Equations to Data (John Wiley
     & Sons, New York, New York).

Dave, J. V. (1970), "Subroutines  for Computing  the Parameters of the
     Electromagnetic Radiation  Scattered by a Sphere,"  IBM System 360
     Program 3600-17.4.002

-------
                                    179
Davis, D. D., W. Heaps, and T. McGee (1976), "Direct Measurements  of
     National Tropospheric Levels of OH Via an Aircraft Borne Tunable
     Dye Laser," Geophys. Res. Letters, Vol. 3, pp. 331-333.

Davis, D. D., G. Smith, and J. Klauber (1974), "Trace Gas  Analysis  of
     Power Plant Plumes Via Aircraft Measurements:   (h, NOX and SO?
     Chemistry," Science. Vol. 186, pp. 733-736.

Durran, D.  D., et al.  (1978),  "A Study of Long Range Air Pollution  Problems
     Related to Coal  Development in the Northern Great Plains,"  Systems
     Applications, Incorporated, San Rafael, California.

Egan, B. A., and J. R. Mahoney (1972), "Numerical Modeling of Advection
     and Diffusion of Urban Area Source Pollutants," J. Appl.  Meteor.,
     Vol. 11, pp. 312-322.

Ensor, D. S., L. E. Sparks, and M.  J. Pilat (1973), "Light Transmittance
     Across Smoke Plumes Downwind from Point Sources of Aerosol  Emissions,"
     Atmos. Environ.,  Vol. 7,  pp. 1267-1277.

EPA (1976a), "1973 National  Emissions Report," EPA-450/2-76-007, National
     Air Data Branch, Office of Air Quality Planning and Standards,
     Environmental Protection  Agency, Research Triangle Park,  North
     Carolina.

           (1976b), "Monitoring and Air Quality Trends Report,  1974,"
     EPA-450/1-76-001, Environmental  Protection  Agency,  Washington,  D.C.

	 (1976c), "Existing and Proposed Fuel  Conversion  Facilities
     Summary," TS-5, EPA Region VIII, Denver,  Colorado.

ER&T (1977),  "Development of an Atmospheric Model  for  Sulfate  Formation,"
     Document No.  P-1534, Environmental  Research & technology,  Incorporated,
     Santa Barbara, California.

Ettinger,  H.  J.,  and G.  W.  Royer (1972),  "Visibility and Mass  Concentra-
     tion  in  a Nonurban  Environment," J.  Air Poll. Contr. Assoc.. Vol. 22,
     PP.  108-m.

Federal  Power Commission (1976),  "FPC Form 67:   Steam  Electric  Plant Air
     and Water Quality Control  Data for  the Year Ending  December 31, 1975,"
     Washington,  D.C.

Forrest,  J.,  and L. Newman (1977a), "Further Studies on  the Oxidation of
     Sulfur Dioxide in Coal-Fired Power  Plant  Plumes," Atmos.  Environ..
     Vol.  11, pp.  465-474.

           (1977b), "Oxidation of Sulfur Dioxide in  the  Sudbury Smelter
     Plume," Atmos. Environ.,  Vol.  11, pp.  517-520.

-------
                                   180
Forsythe,  G.  E.,  and W.  R.  Wasow (1960),  Finite-Difference Methods  for
     Partial  Differential  Equations  (John Wiley &  Sons,  New  York,
     New York).

Foster,  P. M. (1969), "The Oxidation of S02 in Power  Station Plumes,"
     Atmos. Environ., Vol.  3,  pp.  157-175.

Freiberg,  J.  (1975), "The  Mechanism  of Iron Catalyzed Oxidation  of  S02
     in  Oxygenated Solutions," Atmos.  Environ., Vol.  9,  pp.  661-672.

           (1974), "Effects of Relative Humidity and  Temperature on Iron-
     Catalyzed Oxidation of S02 in Atmospheric Aerosols,"  Environ.  Sci.
     Techno! . , Vol.  8,  pp.  731-734.

Friedlander,  S.  K.  (1977),  Smoke,  Dust  and  Haze:   Fundamentals of Aerosol
     Behavior (John  Wiley & Sons,  New York,  New
Fuller, E. C., and R.  H.  Crist (1941),  "The Rate of Oxidation  of Sulfite
     Ions by Oxygen,"  J.  Am.  Chem.  Soc.,  Vol.  63,  pp.  1644-1650.


Galbally, I. F., (1974),  "Gas Transfer Near the Earth's Surface," Advances
     in Geophysics. Vol.  18B, pp.  329-340.

Gartrell, F. E., F. W. Thomas, and S. B.  Carpenter (1963), "Atmospheric
     Oxidation of SO? in Coal -Burning Power Plant Plumes," Am. Ind.  Hyg.
     J_., Vol. 24, pp.  113-120.

Gerhard, E.  R.,  and H. F.  Johnstone (1955), "Photochemical  Oxidation  of
     Sulfur Dioxide in Air,"  Ind.  Eng.  Chem.,  Vol.  47,  p.  972.

Gnanadesikan, R. (1977),  Methods  for Statistical  Data Analysis of Multi-
     yariate Observations  (John Wiley & Sons,  New York,  New York).

Grosjean, P., and S. K.  Friedlander (1975), "Gas-Particle  Distribution
     Factors for Organic  and  Other Pollutants  in the Los Angeles
     Atmosphere," J. Air Poll. Contr. Assoc.,  Vol.  10,  pp.  1038-1044.

Hagen,  L. J., and N. P.  Woodruff  (1973),  "Air  Pollution from Duststorms
     in the Great Plains," Atmos.  Environ.. Vol.  7, pp.  323-332.

Halow,  J. S., and S. J.  Zeek  (1973), "Predicting Ringelmann Number and
     Optical Characteristics  of Plumes,"  J. Air Poll.  Contr. Assoc..
     Vol. 23, pp. 676-684.

Hanson, J. E., and L.  D.  Travis (1974), "Light Scattering  in Planetary
     Atmospherics," Space Science Reviews,  Vol. 16, pp.  527-610.

Heisenberg, W. (1948), "Zur Statistischen Theorie der  Turbulenz," Z_.
     Phys . , Vol. 124,  p.  614.

-------
                                    181
Hidy, G. M., et al.  (1975), "Characterization of Aerosols in California
     (ACHEX)," Science Center, Rockwell  International,  Thousands  Oaks,
     California.

Hodkinson, J. R. (1966), "Calculations of Colour and Visibility in
     Urban Atmospheres Polluted by Gaseous N02," Air Water Poll.  Int.  J.,
     Vol. 10, pp. 137-144.

Holzworth, G. C. (1972), "Mixing Heights, Wind Speeds,  and Potential  for
     Urban Air Pollution Throughout the Contiguous United States," AP-101,
     Office of Air Programs, Environmental Protection Agency,  Research
     Triangle Park,  North Carolina.

Horvath, H. (1972),  "Author's Reply:   On the Brown Colour of Atmospheric
     Haze," Atmos.  Environ. , Vol.  6,  PP- 143-148.

           (1971),  "On the  Brown Colour of Atmospheric  Haze,"  Atmos.
     Environ., Vol.  5, pp.  333-344.

Husar, R. B., and W. H. White (1976), "On the Color of the Los Angeles
     Smog," Atmos. Environ., Vol. 10, pp. 199-204.

Irvine, W. M. (1975), "Multiple Scattering in Planetary Atmospheres,"
     Icarus, Vol. 25, pp. 175-204.

Jarman, R. T., and C. M. DeTurville (1969), "The Visibility and Length
     of Chimney Plumes," Atmos. Environ., Vol. 3, pp. 257-280.

Jerskey, T. N., and C. S. Burton (1977), "The Prediction of Visibility
     on a Regional Scale:  The Status of Visibility Models and Measure-
     ments," El77-23, Systems Applications, Incorporated, San Rafael,
     California.

Johnstone, H. F., and D. R. Coughanowr (1958), "Absorption of Sulfur
     Dioxide from Air:  Oxidation in Drops Containing Dissolved Catalysts,"
     Ind. Enq. Chem., Vol.  50, p. 1169.

Johnstone, H. F., and A. J. Moll (1960), "Formation of Sulfuric Acid in
     Fogs," Ind. Eng. Chem., Vol. 52, p. 861.

Judd, D. B., and G.  Wyszecki (1975), Color in Business Science and
     Industry (John Wiley & Sons, New York, New York).

Junge, C. E. (1963), Air Chemistry and Radioactivity (Academic Press,
     New York, New York]"!

Junge, C. E., and T. G. Ryan (1958), "Study of the S02 Oxidation in
     Solution and Its Role in Atmospheric Chemistry," Quart.- J. Roy.
     Meteor. Soc.. Vol. 84, pp. 46-55.
Katz
,  M.  (1950),  "Photoelectric  Determination  of  Atmospheric  S02  Employ-
 ing  Dilute Starch-Iodine  Solutions,"  Anal. Chem..  Vol. 22, p.  1040.

-------
                                   182
LACAPCD (1971), "Profile of Air Pollution Control,"  Air Pollution  Control
     District, County of Los Angeles,  Los Angeles,  California.

Larson, T.  V., N.  R.  Horike, and H.  Harrison  (1977),  "Oxidation of Sulfur
     Dioxide by Oxygen and Ozone in  Aqueous Solution:   A Kinetic Study
     with Significance to Atmospheric  Rate Processes,"  Atmos. Environ.,
     in press.

Latimer, D. A., and G. S. Samuel sen  (1978),  "Visual  Impact  of Plumes
     from Power Plants," Atmos. Environ., Vol.  12,  pp.  1455-1465.

           (1975), "Visual Impact of Plumes  from Power  Plants," UCI-ARTR-
     75-3, UCI Air Quality Laboratory, School  of Engineering,  University  of
     California, Irvine, California.

Leighton, P.  A. (1961),  Photochemistry of Air  Pollution  (Academic  Press,
     New York, New York).

Levy, A. H.,  D. R. Drewes, and J.  M.  Hales (1976),  "S02  Oxidation  in
     Plumes:   A Review and Assessment of Relevant Mechanistic  and  Rate
     Studies," EPA-450/3-76-022,  Environmental  Protection  Agency,
     Research Triangle Park,  North Carolina.

Liu, M. K., and D. Durran  (1977),  "The Development  of a  Regional Air
     Pollution Model  and Its  Application to the Northern Great Plains.,"
     EPA-908/1-77-001, Systems Applications,  Incorporated, San Rafael,
     California.

           (1976), "On the Modeling of Transport and Diffusion of  Air
     Pollutants over Long Distances," ER76-55,  Systems  Applications,
     Incorporated, San Rafael,  California.

Liu, M. K., M. A. Wojcik, and D.  Henderson  (1978),  "Numerical  Experiments
     of the Effect of Lateral  Diffusion on  Mesoscale Pollutant Dispersion,"
     Summer Computing Conference, 24-26 July 1978,  Newport Beach,
     California.

Matteson, M. J. (1978), "Capture  of Atmospheric Gases by Water Vapor  Con-
     densation on Carbonaceous  Particles,"  Conference on Carbonaceous
     Particles in the Atmosphere, 20-22 March 1978, Lawrence Berkeley
     Laboratory, Berkeley, California.

Matteson, J. J., W. Stober, and H.  Luther (1969), "Kinetics of the
     Oxidation of SOo by Aerosols of Manganese Sulfate," Ind.  Eng. Chem.
     Fund., Vol. 8, pp. 677-687.

McKay, H.A.C. (1971), "The Atmospheric Oxidation of Sulphur Dioxide in
     Water Droplets in Presence of Ammonia," Atmos. Envi ron..  Vol. 5,
     pp. 7-14.

Megaw, W. J. (1977), "Thin Layer  Brown Haze," J. Aerosol Sci., Vol. 8,
     pp. 21-29.

-------
                                   183
Middleton, W.E.K.  (1952),  Vision Through  the Atmosphere  (University  of
     Toronto Press,  Toronto,  Canada).

Miller, J. M., and R.  G.  DePena, (1972),  "Contribution of Scavenged
     S02 to the Sulfate Content of Rain Water,"  J.  Geophys.  Res.,
     Vol. 77, pp.  5905-5916.

Morrison, D. F. (1976), Multivariate  Statistical  Methods  (McGraw-Hill,
     New York, New York).

Munsell Color Company  (1976), "Munsell  Book  of Color," Baltimore,
     Maryland.

Newman, L., J. Forrest, and B.  Manowitz (1975),  "The  Application of  an
     Isotopic Ratio Technique to a Study  of  the  Atmospheric  Oxidation
     of Sulfur Dioxide in  the Plume from  an  Oil-Fired Power  Plant,"
     Atmos. Environ.,  Vol.  9, pp.  959-968.

NGPRP (1974), "Atmospheric  Aspects Work Group Report," Northern Great
     Plains Resource Program, Denver, Colorado.

Niki, H. (1974), "Reaction Kinetics Involving 0  and N Compounds,"  Can.
     J. Chem., Vol.  52, pp. 1397-1404.

Nixon, J. K. (1940), "Absorption Coefficient of  Nitrogen  Dioxide in  the
     Visible Spectrum," J.  Chem. Phys.. Vol. 8,  pp. 157-160.

Noll, K. E., P. K. Mueller, and M. Imada  (1968),  "Visibility and
     Aerosol Concentration in Urban Atmospheres," Atmos.  Environ.,
     Vol. 2, pp. 465-475.

Nordlund, G. G. (1975), "A Quasi-Lagrangian  Cell  Method  for  Calculating
     Long-Distance Transport of Airborne  Pollutants," J.  Appl.  Meteor.,
     Vol. 14, pp.  1095-1104.

Nordo, J. (1973),  "Meso-Scale and Large-Scale Transport  of Air  Pollutants,"
     Proc. Third International  Clean  Air  Congress,  B105-B108, Dusseldorf,
     Federal Republic  of Germany,  VDI-Verlag.

Nordo, J., A. Eliassen, and J.  Saltbones  (1974),  "Large-Scale Transport  of
     Air Pollutants,"  Advances  in Geophysics. Vol.  18B,  pp.  137-150.

Novakoy, T., S. G. Chang,  and A. B. Marker (1974),  "Sulfates in Pollu-
     tion Particulates:  Catalytic Oxidation of S02 on Carbon Particles,"
     Science, Vol. 186, pp. 259-261.

Orel, A. E., and J.  H. Seinfeld (1977), "Nitrate Formation in Atmospheric
     Aerosols," Environ.  Sci. Techno!., Vol. 11,  pp.  1000-1007.

Payne, W. A., L. 0.  Stief,  and D.  D.  Davis  (1973),  "A Kinetics  Study of
     the Reaction of H02 with $03 and NO," J. Am. Chem.  Soc.. Vol. 95,
     pp. 7614-7619.

-------
                                   184
 Penkett, S. A.  (1972), "Oxidation of SC>2 and Other Atmospheric Gases by
     Ozone  in Aqueous Solution," Nature, Phys. Sci., Vol. 240, pp. 105-106.

 Penkett, S. A., and J. A. Garland (1974), "Oxidation of SO? in Artificial
     Fogs by Ozone," Tell us, Vol. 26, pp. 284-290.

 Pilat, M. J., and D. S. Ensor (1971), "Comparison Between the Light
     Extinction Aerosol Mass Concentration Relationship of Amtospheric
     and Air Pollutant Emission Aerosol," Atmos. Environ., Vol. 5,
     pp. 209-215.

Roberts,  E.  M,,  et al.  (1975),  "Visibility  Measurements  in  the Painted
     Desert Through  Photographic Photometry,"  Engineering  Bulletin 47,
     Dames  & Moore,  Santa Barbara,  California.

Roberts,  P.  T.,  and  S.  K.  Friedlander  (1975),  "Conversion of $03 to
     Sulfur  Particulate  in  the Los Angeles  Atmosphere,"  Environ. Health
     Perspectives, Vol.  10,  pp.  103-108.

Rodhe,  H. (1972),  "A Study of the Sulphur Budget  for the Atmosphere over
     Northern Europe,"  Tell us.  Vol.  24,  pp.  128-138.

Samuels,  H.  J.,  S. Twiss, and E. W.  Wong (1973),  "Visibility,  Light
     Scattering and Mass Concentration of Particulate Matter,"
     California Air Resources Board, Sacramento,  California.

Sander, S.  P.,  and J.  H. Seinfeld (1976), "Chemical  Kinetics  of Homogeneous
     Atmospheric Oxidation of Sulfur Dioxide," Environ.  Sci.  Techno!.,
     Vol. 10, pp.  1114-1123.

Schroeter,  L. C. (1963), "Kinetics of Air Oxidation  of Sulfurous Acid
     Salts," J.  Pharm.  Sci.. Vol. 52,  pp. 559-563.

Schwartz, S. E., and L. Newman (1978), "Processes Limiting Oxidation of
     Sulfur Dioxide in Stack Plumes,"  Environ. Sci.  Techno!.,  Vol. 12,
     No.  1,  pp.  67-73.

Scott, W. D., and P. V. Hobbs (1967),  "The Formation of Sulfate in Water
     Droplets," J. Atmos. Sci..  Vol. 24, pp. 54-57.

Scriven,  R.  A.,  and B.E.A. Fisher (1975a),  "The Long-Range Transport of
     Airborne Material  and Its Removal by Deposition and Washout--
     I.  General Considerations," Atmos. Environ.,  Vol.  9, pp. 49-58.

            (1975b),  "The Long-Range Transport of Airborne Material and
     Its Removal by Deposition and Washout--!!.  The Effect of Turbulent
     Diffusion," Atmos. Environ., Vol. 9, pp. 59-68.

Sellers, W. D. (1965), Physical Climatology (University of Chicago Press,
     Chicago, Illinois).

-------
                                    185
Smagorinsky, J. (1963), "General Circulation Experiments with the Primitive
     Equations:  I.  The Basic Experiment," Mon.  Wea.  Rev..  Vol. 91,
     pp. 99-164.

Spicer, C. W.,  and P. M. Schumacher (1977), "Interferences in Sampling
     Atmospheric Particulate Nitrate," Atmos. Environ., Vol.  11, pp. 873-876.

Thorn, A. S. (1972), "Momentum,  Mass and Heat Exchange  of Vegetation,"
     Quart. J. Roy. Met. Soc.,  Vol. 98, pp. 124-134.

Trijonis, J., and K.  Yuan (1978), "Visibility in  the Northeast:   Visibility
     Trends and Visibility/Pollutant Relationships," Technology  Service
     Corporation,  Santa Monica, California.

           (1977),  "Visibility  in the Southwest:   An Exploration of the
     Historical Data Base," Technology Service Corporation,  Santa Monica,
     California.

Urone, P., and W. H. Schroeder (1969), "S02 in the Atmosphere:   A Wealth
     of Monitoring Data but Few Reaction Rate Studies," Environ.  Sci.
     Techno!.. Vol. 3, pp. 436-445.

Urone, P., et al. (1968), "Static Studies of Sulfur Dioxide  Reactions  in
     Air," Environ. Sci. Technol., Vol. 2, pp. 611-618.

van der Heuvel, A. P., and B.  J.  Mason (1963), "The Formation of Ammonium
     Sulfate in Water Droplets Exposed to Gaseous  S02  and  NH3,"  Quart.  J.
     Roy.  Meteor. Soc.. Vol.  89,  pp.  271-275.

Van de Hulst,  H. C. (1957), Light Scattering by Small  Particles  (John
     Wiley & Sons, New York,  New  York).

Waggoner,  A. P., and R. J. Charlson  (1971), "Simulating the  Color of
     Polluted  Air," Applied Optics.  Vol.  10, pp. 957-958.

Waggoner,  A. P., R. J. Charlson,  and  N. C. Ahlquist (1972),  "Discussion:
     On the Brown Color of Atmospheric Haze,"  Atmos. Environ., Vol. 6,
     pp. 143-148.

Waggoner,  A. P., et al. (1976),  "Sulfate-Light Scattering  Ratio  as an
     Index of  the Role of Sulfur  in Tropospheric Optics,"  Nature.
     Vol.  261, pp. 120-122.

Weir, A.,  et al. (1976), "Factors Influencing  Plume Opacity," Environ.
     Sci.  Techno!., Vol. 10,  pp.  539-544.

           (1975), "Measurement of Particle Size and Other Factors Influ-
     encing Plume Opacity,"  International  Conference on  Environmental
     Sensing and Assessment,  14-19 September 1975,  Las Vegas,  Nevada.

-------
                                  186
Whitby, K. T., and G.  M.  Sverdrup (1978),  "California Aerosols:   Their
     Physical  and Chemical  Characteristics,"  to be published in  the
     ACHEX Hutchinson  Memorial  Volume,  Particle Technology Laboratory
     Publication Number 347,  University of Minnesota, Minneapolis,
     Minnesota.

White, VI. H. (1977),  "NOX-03 Photochemistry in Power Plant Plumes:
     Comparison of Theory with  Observation,"  Environ. Sci. Techno!.,
     Vol. 11,  No. 10,  pp. 995-1000.

White, W. H.,  and P. T. Roberts (1975), "The  Nature and Origins  of
     Visibility Reducing Aerosols in Los Angeles," 68th Annual Meeting,
     Air Pollution Control  Association, 15-20 June 1975, Boston,
     Massachusetts.

Whitten, G. Z., and H. Hogo (1977),  "Mathematical  Modeling of Simulated
     Photochemical Smog," EPA-600/3-77-001, Systems Applications,
     Incorporated, San Rafael,  California.

Williams, M. D., and R. Cudney  (1976),  "Predictions and Measurements  of
     Power Plant Plume Visibility Reductions  and Terrain Interactions,"
     Proc. of the Third Symposium on Atmospheric Turbulence Diffusion
     and Air Quality,  American  Meteorological Society, pp. 415-420.

Williams, M. D., M. J. Wecksung,  and E. M. Leonard (1978), "Computer
     Simulation of the Visual Effects of Smoke Plumes," Society  of  Photo-
     Optical Instrumentation Engineers  Technical  Symposium, 30 March  1978,
     Washington, D.C.


Winkelmann, D.  (1955), "Die Electrochemische Messung du Oxidations-
     geschwindigkeit  von Na?S03 Durch Gelosten Sauerstoff," Z.  Elektrochemie,
     Vol. 59, pp. 891-895.

Winkler, P. (1973), "The Growth of Atmospheric Aerosol Particles as a
     Function of the  Relative Humidity--!I.  An Improved Concept of
     Mixed Nuclei," Aerosol Sci., Vol. 4, pp. 373-387.

Yanenko, N. N.  (1971), The Method of Fractional Steps (Springer-Verlag,
     Berlin, Germany).

-------
                                   187
                                GLOSSARY
accumulation mode--Submicron particles in the range  0.1  to  1.0  ym, which
     are formed from smaller nuclei  by coagulation or  by direct conden-
     sation of gases.  This particle mode is  most effective per unit mass
     in light scattering.   Secondary particles such  as sulfates,  nitrates,
     and organics are found predominantly in  this size range.   Since coag-
     ulation is relatively slow for  particles larger than 1  ym,  particles
     in the accumulation mode are generally removed  from the atmosphere by
     precipitation and surface deposition before they  grow  larger.

aerosol—A suspension of fine solid  or liquid particles  in  air  or a gas.
     In the context of visibility impairment, aerosol  means  a suspension of
     nuclei, accumulation mode, and  coarse particles (and gaseous pollutants)
     in ambient air.   Aerosol is also sometimes used to  signify the liquid
     or solid particles themselves.

anthropogenic—Caused directly by man or indirectly  by man's technology
     (e.g., anthropogenic  pollutant  emissions from combustion sources  such
     as automobiles and boilers).

a'ppearance--The subjective visual  impression  or aspect of a  thing observed
     by a human (e.g., the appearance of distant mountains  or a plume).

atmospheric discoloration—An imprecise term  describing  the  change in  color
     of the sky or distant mountains or clouds observed  through the atmos-
     phere due to natural  or man-made pollution.  The  term  implies that
     there is an atmospheric color or set of  colors  that can be defined
     as natural and not discolored.   Examples of atmospheric discoloration
     are white, grey, yellow, brown, or black haze or  plumes.

background—An object being viewed by an observer (e.g.,  sky, cloud, or
     mountain).  Light reflected (if any)  from the object and light scat-
     tered and absorbed by the atmosphere along the  sight path  or line of
     sight between the object and the observer determines the color per-
     ceived by the observer.  The nature of the background  affects the
     apparent coloration of a plume  or haze layer.

back scatter—Situation where the sun is behind the  observer (e>90°).

chroma—The numerical index in the Munsell  color notation system that
     describes the degree  of saturation or the departure  from grey.  A
     chroma of 0 is grey;  a chroma of 2 is slightly  colored; a  chroma  of
     6 is highly colored.

-------
                                   188
chromaticity diagram and coordinates—A mathematical description of the
     relative spectral  distribution  (hue  and  saturation) of a given color.
     Chromaticity coordinates  uniquely describe  the  position of a given
     color on a two-dimensional  plot called a chromaticity plot.  Chroma-
     ticity coordinates provide  information only on  the relative mix of
     light of different wavelengths,  not  the  overall light intensity or
     luminance.  For example,  chromaticity coordinates are not sufficient
     to describe the difference  between yellow and brown (a dark yellow).

C.I.E.--Commission Internationale de 1'Eclairage, or International Commission
     on Illumination, a scientific organization  responsible for setting stan-
     dards for light and color measurement and specification.

Class I areas—Areas such as  national parks,  wilderness areas, and national
     forests that are afforded the most stringent air quality protection
     both in terms of the significant deterioration  air quality increments
     and the visibility protection and restoration mandates of the Clean
     Air Act (Section 169).   Mandatory Class  I areas are those areas desig-
     nated as such by the legislature; however,  Class II areas may be redes-
     ignated as Class I.

coagulation—The process of  particle growth resulting from particle collision,

coarse particles—Particles  larger than 1 ym, caused principally by grinding
     and mechanical  process  (e.g., soil dust).

color difference parameter (A£)—An  index quantifying the difference between
     two colors, in terms of light intensity  differences as we'll as chroma-
     ticity differences, transformed such that equal values of AE correspond
     to equally perceived differences.  The parameter is useful to character-
     ize the overall perceptibility  of haze layers resulting from color
     differences.

color solid or volume—A three-dimensional representation of color.  A color
     can be located in a color volume by  specifying  Munsell hue, value, and
     chroma or by specifying overall  light intensity or luminance (Y) and
     chromaticity coordinates  (x, y).  The color difference parameter (A£)
     may be visualized as a  distance between  two points in a color volume
     which has been transformed  such that"equal  distances correspond to
     equally perceived color differences.

contrast—The fractional difference  in light  intensities of two colors.  The
     contrast defined at specific wavelengths of light  is useful in charac-
     terizing color changes.   The contrast between a black object and the
     clear, horizon sky is used  in defining visual range.

diffuse radiation—See "multiple scattering."

elevation angle (g)--Angle between the horizontal and the line of sight
     (sight path).

-------
                                   189
extinction coefficient (bext)"The derivative of transmitted  light  intensity
     with respect to distance along a sight path of light attenuation  due  to
     light scatter and absorption.  The extinction coefficient  is a  function
     of wavelength and depends on concentrations and characteristics of
     aerosol particles and absorbing gases such as NO;?.   The  extinction
     coefficient is the sum of the scattering coefficient (bscat) anc'  the
     absorption coefficient (baDS).

fly ash—Primary particulate matter emitted from furnaces and boilers,
     usually consisting chiefly of silica with traces of oxides of metals
     such as aluminum and iron.  Plume opacity at the top of  a  stack is  usu-
     ally caused by fly ash.

forward scatter—Situation where the sun is in front of  the observer so
     that direct solar radiation is scattered less  than  90° into the
     observer's line of sight (e<90°).

hue—Index in the Munsell  color notation system characterizing  the dominant
     coloration (e.g., red, green, or blue).

integrating nephelometry—A technique that measures the  scattering coeffi-
     cient of a small  volume of air within a  chamber.

Koschmieder relationship--The mathematical  expression for calculating  the
     visual range in a homogeneous atmosphere:


                                r  = 3.912

                                 v    bext
liminal contrast—The contrast that is  barely  perceptible.  This contrast
     threshold will  depend on the observer  and lighting  conditions, but a
     liminal contrast of 0.02 is common and is used  in the definition of
     visual range.

line of sight (or sight path)—The line connecting the observer and the
     observed object.  Particles and gases  in  the atmosphere along this
     line will affect the perceived color of the object  by absorbing light
     and by scattering light into and out of the line of sight.

luminance (Y)--The overall light intensity  within the visible spectrum,
     weighted by the photopic response  of the  human  eye.

Mie scatter!ng--The theory describing scattering of  electromagnetic
     radiation by spherical  particles of diameters of the same order as
     the wavelength (A) of the radiation.   Rayleigh  scattering theory
     covers scattering by particles with diameters much  shorter than A.

multiple scattering—Radiation that has been scattered more than once.
     Single scattering results when direct  solar radiation is scattered into

-------
                                  190
     the line of sight.   Multiple  scattering occurs when direct solar
     radiation is scattered at least  once  by gases and particles not in
     the line of sight or is reflected  from the  surface of the earth or
     clouds before being scattered by particles  and gases along the line of
     sight.  Diffuse radiation has been scattered or reflected at least
     once, while direct solar radiation, as its  name implies, is radiation
     directly from the sun.

Munsell  color notation—A system of describing a color quantitatively by
     reference to three indices (hue, value, and chroma).  The Munsell Book
     of Color displays color paint chips at specific intervals of hue, value,
     and chroma.

nuclei mode—Particles less than 0.1  ym in diameter, which are not effective
     in light scattering, but grow by coagulation to the accumulation mode.

opacity—A term characterizing the optical thickness of an aerosol layer,
     usually used to characterize  smoke plumes in or near the stack.  Opacity
     is usually expressed in percent  and is defined as


                     Opacity = 1 - Transmittance    ,


     where transmittance is related to  the optical thickness T as follows:


               Transmittance = e~T
optical thickness (T)—The integral  of the  extinction  coefficient of an aero-
     sol between two points along  a  given line  of  sight.

particulate matter—Small  solid or liquid particles, consisting of many mole-
     cules, that are suspended in  air.

perceptibility—As used herein, the  characteristic of  an object that makes
     it visible to a human observer.   Perceptibility results from differ-
     ences in light intensity and  color between two objects.  For example,
     a distant mountain is perceptible because  it  is darker than the back-
     ground sky.  Air pollution is perceptible  if  color differences exist
     between a plume and a background,  a haze layer and a capping layer, or
     between a haze and a recollection of a clear  day.  (See also "liminal
     contrast").

phase function—See "scattering distribution function."

pollutant flux—The total  mass of  a  pollutant species  in a plume passing
     through a plane perpendicular to the plume centerline per unit of time.

primary particulate—Particles emitted directly from an emissions source
     (e.g., fly ash).

-------
                                  19.1
Rayleigh scattering—The theory describing scattering of radiation by
     molecules or particles much smaller than the wavelength of the radi-
     ation, resulting from a dipole interaction with the electric field
     of the radiation.

saturation—See "chroma."

scattering angle—The angle between the vector describing the unscattered
     radiation on an object and the vector along the line of sight between
     the object and the observer.

scattering distribution function (or phase function)--The function describing
     the direction in which radiation is scattered.   For aerosols the scat-
     tering distribution function is largest in forward scatter (e<45°),
     which explains why haze layers are bright when  the sun is in front of
     the observer.
                                                     2
solar flux--The intensity of solar radiation (watts/m ) incident on a given
     plane perpendicular to the solar rays.

spectral light intensity—The light?intensity along  a particular line of
     sight at wavelength A (watts/m /steradian).   The spectral  light inten-
     sity can be considered the increment of radiant energy of wavelength A
     to A + dA passing through an elemental  area  dA  within a solid angle dw
     along the given line of sight:
telephotometry--A technique for measuring the light  intensity  of  a  distant
     object using a photometer coupled to a  telescope.   By measuring  the
     differences in light intensity between  the  clear  horizon  sky and dis-
     tant mountains, one can estimate the visual  range.

transmissometry—A technique of measuring the transmission of  light through
     the atmosphere by which the overall  extinction  can  be determined.

tristimulus values—Indices that describe a  given color  by indicating the
     amount of red, green,  and blue light needed  to  match the  color.  Tris-
     timulus values (X, Y,  Z)  are keyed to the wavelength responses of  the
     three color sensors in the human eye.   They  can also be translated
     into chromaticity coordinates (x, y).

value—The index in Munsell  color notation related to  brightness  (luminance
     or overall  light intensity).

visibility—See "visual range."

visibility impairment—A reduction in visual  range,  the  presence  of atmos-
     pheric discoloration,  or both.   The  Clean Air Act Amendments of  1977

-------
                                  192
     refer to "any"  and  "significant" visibility impairment, terms which
     have yet to be  defined  in  regulations.

visual  range (or visibility)--The distance at which a large, black object
     is barely visible when  viewed against the horizon sky.  For calculations,
     it is convenient to use a  more  strict definition of visual range, i.e.,
     the distance at which the  contrast  between a black object and the clear
     (cloudless) horizon sky is reduced  to 0.02.  When calculating contrast,
     one should use  overall  light intensity or luminance (Y) or, as an approx-
     imation, the spectral light intensity at X = 0.55 ym, which is the mid-
     point of the visible spectrum and the wavelength to which the human eye
     is most sensitive.

zenith  angle—The angle  between the  solar beam and the vertical at a given
     location on Earth.

-------
                                           193
TECHNICAL fJEPOHT DATA
({'lease read linlruc nuns un il r rcrcnc liclnrc cotni'lvtittfl
1. REPORT NO. 2.
EPA-450/3-78-nOa,b,c
4. TITLE AND SUBTITLE
THE DEVELOPMENT OF MATHEMATICAL MODELS FOR THE
•PREDICTION OF ANTHROPOGENIC VISIBILITY IMPAIRMENT
7. AUTHOR(S)
D. A. Latimer, R. W. Bergstron, S. R. Hayes, M. K. Liu,
J. H. Seinfeld, G. Z. Whitten, M. A. Wojcik, M.d. Hillye
9. PERFORMING ORGANIZATION NAME AND ADDRESS
Systems Applications, Incorporated
950 Northgate Drive
San Rafael, California 94903
12. SPONSORING AGENCY NAME AND ADDRESS
U. S. Environmental Protection Agency
Waterside Mall
401 M Street, S.W.
Washington, D.C. 20460
3. RECIPIENT'S ACCESSION-NO.
6, REPORT DATE
November 1 978
6. PERFORMING ORGANIZATION CODE
8. PERFORMING ORGANIZATION REPORT NO.
» EF78-68A,B,C
10. PROGRAM ELEMENT NO.
11. CONTRACT/GRANT NO.
EPA 68-01-3947. and 68-02-2593
13. TYPE OF REPORT AND PERIOD COVERED
Rnal Report: 10/77 to 9/78
14. SPONSORING AGENCY CODE
EPA-OPE/OAQPS
15. SUPPLEMENTARY NOTES
16. ABSTRACT
    This  report  describes a  nine-month  study  to  recommend  and  develop  models  that pre-
  dict  the contribution of man-made  air  pollution to  visibility impairment  in  federal
  Class  I  areas.  Two models  were  developed.   A near-source plume  model  based  on  a
  Gaussian formulation was designed  to compute the impact of a  plume  on visual  range
  and atmospheric coloration.  A regional model was designed to calculate pollutant
  concentrations  and visibility impairment  resulting  from emissions from multiple
  sources  within  a  region with a spatial scale of 1000  km and a temporal scale of
  several  days.   The objective of  this effort  was to  develop models that are useful
  predictive tools  for making policy and regulatory decisions,  for evaluating  the
  impacts  of proposed new sources, and for  determining  the  amount  of  emissions reduc-
  tion  required from existing sources, as mandated by the Clean Air Act Amendments
  of 1977.  Volume I of this  report contains the  main  text;  Volume II  contains  the
  appendices;  Volume III  presents  case studies of power plant plume visual  impact for
  a  variety of emission,  meteorological, and ambient  background scenarios.
17. KEY WORDS AND DOCUMENT ANALYSIS
». DESCRIPTORS
Air quality modeling
Visual range
Atmospheric discoloration
Power plants
18. DISTRIBUTION STATEMENT
RELEASE TO PUBLIC
b.lDENTIFlERS/OPEN ENDED TERMS

19. SECURITY CLASS (TltisKvpon)
UNCLASSIFIED
20. SECURITY CLASS (Tliit pancj
UNCLASSIFIED
c. COSATI i icid/Group

Vo. 'II--494J
22. PRICE
Vol. III--91
(PA farm 2220-1 (9-73)

-------
                             3  <£
                             0)  Q)
                          33OO
                          CT  -5 -£
                          y)  —  —
                          CD  o  n
                          Q3  fD  ttl
                              >z
m > TJ m TI ~
     § 3  5.0,
        I    a

-------