August 12, 1999

EP A-SAB-COUNCIL-ADV-99-013

Honorable Carol M. Browner
Administrator
U. S. Environmental Protection Agency
401 M Street, SW
Washington, DC 20460
                    RE:   The Clean Air Act Amendments (CAAA) Section 812 Prospective
                           Study of Costs and Benefits (1999 ): Advisory by the Air Quality
                           Models Subcommittee on Modeling and Emissions
Dear Ms. Browner:
       On May 4 and 5, 1999, the Air Quality Models Subcommittee (AQMS) of the Advisory
Council on Clean Air Compliance Analysis (Council) met to provide advice on six charge
questions relating to trends in ambient concentrations of air pollutants associated with
implementation of the 1990 Clean Air Act Amendments (CAAA of 1990, Section 812, Public
Law 101-549, November 15, 1990, 104 Stat. 2399) projected to the year 2010.  The
Subcommittee reviewed draft material and received briefings from Agency staff and contractors.
The AQMS also held a public teleconference call on June 3, 1999 to review and advise the
Agency on additional aspects of the study analysis including primary Particulate Matter (PM)
emissions, temporal and spatial extrapolation of air quality data, and emissions and air quality
modeling uncertainty tables. The Council met on July 13-14, 1999 to review the draft study, The
Benefits and Costs of the Clean Air Act, 1990 to 2010; EPA Report to Congress (U.S. EPA,
Office of Air and Radiation and Office of Policy, June 1999) which presented an analysis of the
costs and benefits associated with implementation of the CAAA. The analysis was based, in part,
on emissions estimates and air quality reviewed by the AQMS and discussed in this letter.

       This  AQMS Advisory commends the Agency for the progress made since our last
Advisory over a year ago. Many of our major concerns have been addressed and we believe that
the current Prospective Study can proceed. In this letter, we are providing advice on three
levels: (1) assumptions in the analysis, uncertainties in the results, and implications  for overall
conclusions that need to be more clearly discussed in the current Prospective Study; (2) changes
in the general modeling approach, data bases and analysis to be used in the next prospective
study; and (3) recommendations for Agency-wide review of emissions models to enhance
validity not only of this 812 Prospective Study, but also other studies. We believe the
recommendations calling for review of emission estimation procedures and comparison of
emission estimates  to observed pollutant concentrations will improve the basis for air quality
planning by  strengthening the projections of future trends in air pollutants.

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       This Advisory also identifies gaps in information, data, and methods that need to be filled
to strengthen future prospective studies, which the CAAA requires to be submitted to Congress
every two years. The current 812 Study will be the first prospective analysis. It is expected that
the comprehensiveness of the analysis will increase over time, especially as further research
becomes available for use in model simulations of emissions, exposure, health and ecological
effects, and cost and benefits.

       Future prospective studies could benefit greatly from the recommended Agency-wide
analysis of emissions modeling, use of the same, high quality air quality modeling system
platform (such as EPA's Models-3) across the entire United States, and further  exploration of
more robust techniques for dealing with uncertainties in complex assessments.  The AQMS will
be available for providing additional details on how these recommendations could be
implemented in preparation for the next prospective study.

       For the current study, the AQMS recommended orally at our meeting on May 3-4, 1999
that the Agency describe the uncertainties associated with the analytical tools and data used and
how those uncertainties could affect the air quality trends analysis and impact the cost/benefit
analysis.  We have recommended that these considerations be summarized at each step in the
analysis in tables that include the data and tools, their limitations, the implications of the
limitations for study results, and to the extent possible,  provide an estimate of the uncertainty in
the findings that result.  The Agency responded with a proposed approach that was distributed to
the AQMS and discussed at our teleconference on June 3, 1999.  The Subcommittee  generally
found the proposed approach appropriate  for the current Prospective Study.

Response to Charge Questions Posed by the Office of Air and Radiation

       Charge Question 1. Are the input data used for each component of the analysis
sufficiently valid and reliable for the intended analytical purpose?

       Response.  Yes, the input data are sufficient for the current version, with the  following
reservations. It will be  necessary to improve the input data for subsequent versions by
considering the  following recommendations, listed in order of importance.

       The AQMS interprets input data to include the emissions estimates that  are used  in the air
quality modeling, the results of the air quality modeling, the measured concentration  data that are
used with the modeling data to determine future air quality trends, and the final resulting air
quality trends that are the input for the benefit / cost analyses.

       With respect to  the emissions inventory information, we recommended in  our oral
comments to the Agency on May 4-5, 1999 that the discrepancies between the  partitioning of
the PM sources based on the inventory of emissions versus partitioning based on observational
data for PM be  discussed in the report. We note,  based on our conference call  of June 3, 1999,
that the Agency is planning to respond to this recommendation.More detail on this issue  is
provided in our response to Question 4.  In addition, current controversies over volatile organic

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carbon (VOC) emissions and particulate carbonaceous emissions from the transportation sector
need to be noted.  The observational data limitations with respect to PM and ozone need
discussion.

The 812 Study provides processes for specifying quality of the concentration data used.
However, as noted in more detail in the discussions for Charges 5 and 6, we recommend that the
Agency carefully assess the use of the data and the techniques for treating data gaps.  The air
quality models, as well as the data processing tools used to develop the projected air quality
trends for use in the cost/benefit analyses, are discussed in the response to Charge 2.Each of the
limitations and the impacts of these data limitations on the resulting data set needs to be
succinctly presented in the report. By providing a careful analysis of uncertainty and its
implications for the findings and next steps in the impacts analysis, the limits in the cost and
benefit conclusions reachable by the current Prospective Study will be clarified.

       Charge Question 2.  Are the models, and the methodologies they employ, used for each
component of the analysis sufficiently valid and reliable for the intended analytical purpose?

       Response.  The AQMS interprets the Charge Question to pertain to the emission models
used to develop the emissions data,  the air quality models used to develop projected air quality
concentrations, and the techniques used to develop adjustment factors and fill data gaps (i.e.,
establish trends at locations where there are no observational data available).  Our responses to
Charges 5 and 6 below provide more detail to the techniques for developing adjustment factors
and filling data gaps.

       As noted in our response to Question 1, we strongly recommended in our oral  advice on
May 4-5, 1999 that the Agency summarize the model limitations and their impact on the analysis
findings.  We observe, based on  materials provided for the June 3, 1999 teleconference call, that
the Agency is proposing  such a summary in a concise table format, based on the model used for
the Retrospective Study.  The Subcommittee finds that a summary in such a format would be
useful, but has not reviewed the  content.

       For the next Prospective Study, we recommend careful assessment of the overall
approach to emissions modeling  and evaluation of resulting emissions in light of measured
components of particulate matter and of air quality data trends. In addition, we recommend the
use of a single, much more comprehensive modeling system platform (such as EPAModels-3)
allowing use of consistent, appropriate and best available process descriptions throughout the
country.  This advice echoes recommendations in our January 1998 Letter Advisory (The CAA
Section 812 Prospective Study of Costs and Benefits-Air Quality Models and Emissions
Estimates Initial Studies, EPA-SAB-COUNCIL-ADV-98-002 ) on the 812 Study. We
understand that Models-3 may be available for the next Prospective Study and, if so, use of this
model should be considered.  Comprehensive review of the emissions inventory development
process and resulting estimates, with particular emphasis on  the reconciliation of emission
inventory estimates and modeling results with ambient measurements, is needed to strengthen
many other studies in addition to the 812 Study. For the  current study, the Agency needs to

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outline carefully the limitations of the models that were used, along with the implications of these
limitations for the overall study results.

       Charge Question 3.  If the answers to either of the two questions above is negative, what
specific alternative assumptions, data or methodologies does the Council recommend the Agency
consider using for the first prospective analysis?

       Response:  To reiterate, the AQMS suggests that limitations and implications be
presented in a table at each major step of the analysis (i.e., emission estimates, air quality
analyses, adjustment factor derivation and data gap treatment). These descriptions of
uncertainties need to clearly distinguish between those associated with data availability and
analysis and model formulations and limitations.  We also recommend that the Prospective Study
team follow our suggestions regarding use of the  Voronoi Neighbor Averaging (VNA) technique
as is outlined in our response to Question 6. We  also emphasize the need to explore use of the
same modeling system across the United States in the next Prospective Study.

       Charge Question 4.  Do the revisions made to the particulate matter emissions
inventories — as described in the draft Report to  Congress Emissions Appendix— adequately
address the concerns raised by the Council and the AQMS during the January - February 1998
review meetings?  If not, are there further adjustments which the Council and AQMS would
recommend be made in future assessments; and do residual potential errors in the inventories
warrant —in the judgment of the Council and AQMS--  inclusion in EPA's pending report specific
caveats regarding the magnitude and direction of potential biases which might be introduced
through reliance on these inventories?

       Response.  We compliment EPA's effort to improve the emissions estimates used in this
Prospective Study. The primary PM emissions inventory now partially reflects the downward
direction present in the ambient measurement data sets.  We note that the Agency has responded
to oral advice we gave in May by developing a method to reduce the discrepancy between
emissions category partitioning for the PM and observational data for PM.  The Subcommittee
will need to analyze more detailed information on the methodologies used for these adjustments
before it can comment fully on the technical basis for the adjustments.

       The current Criteria Document for PM, Air Quality Criteria for Particulate Matter
(EPA/600/P-95/001aF/cF, 1996), has pie charts  that show typical crustal contributions to PM
2.5 and PM 10 in both eastern and western cities based on air quality observations.  The AQMS
concurs that the urban crustal component of PM  2.5 is on the order of 10 per cent or less of the
mass based on ambient data. The inventories used in this Prospective Study indicate that crustal
material constitutes more than half of the directly emitted PM 2.5. The Subcommittee recognizes
that the deposition rate of larger, crustal components of PM 2.5 is greater than that of smaller,
combustion generated particles and this difference can therefore reduce the subsequent
downwind concentration of crustal derived particles relative to combustion generated particles.
However, the Subcommittee believes that the ratio of crustal to combustion emission rates was
substantially overestimated in the analysis reviewed at the May 4-5 meeting.

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       The further analysis of crustal material emission estimates reviewed at the June 3, 1999
teleconference call appears to be a substantial move in the right direction.  The further analysis
indicating a larger contribution of carbonaceous materials from diesel vehicles also appears to be
in the right direction. The available emissions data on gasoline powered vehicles remain
inadequate to produce emission inventory estimates large enough to account for attribution
(based on tracer compounds of motor vehicle emissions measured in ambient air) of the
carbonaceous component of ambient PM 2.5 to these vehicles in different parts of the country.

       The AQMS wishes to comment further on the deficiencies in the emissions inventory that
relate to this issue.  The Subcommittee believes that one explanation for the discrepancy between
emissions category partitioning and observational data for PM could be that emission inventories
underestimate the directly emitted carbonaceous material. Data from both the Los Angeles basin
and from the Northern Front Range Air Quality Study indicate that carbonaceous emissions from
the fleet of spark ignition vehicles are of the same order of magnitude as emissions from the
diesel fleet. Detailed analysis of ambient data from the  Los Angeles basin shows that diesel and
gasoline mobile sources contribute about  30 to 50 per cent of the  approximately 7 ji/m^ average
organic carbon concentration in the downtown Los Angeles area1. In this area sulfate plus nitrate
and ammonium make up about 12 ji/m^.  The Schauer Study shows that ambient concentrations
of primary organic materials in the PM 2.5 fraction are over three times as high as would be
indicated from crustal emissions.

       This finding is consistent with the Sepulveda tunnel study which showed that organic and
elemental carbonaceous materials were responsible for 30 to 40 per cent of the PM 2.5 in the
tunnel, and that crustal material contributed only 7.8 percent of the PM 2.5.2 The Subcommittee
members have the impression that the ratio of exhaust emissions to crustal emissions from the
roadway shown in the Cadle et al. review is indicative of the ratio of actual emissions
determining particulate air quality in the United States.

        The available information strongly suggests that mobile source carbonaceous emissions
are currently large contributors to public exposure to PM 2.5 and that they are underestimated in
current emission inventories.  As a result, we think that the current draft 812 Prospective Study
does not include a reliable means for estimating the extent to which mobile source programs
under the CAAA provisions would reduce public exposure to carbonaceous material.  The study
       1 Schauer, James J.; Rogge, Wolfgang F.; Flildemann, Lynn M.; Mazurek, Monica A.;
Cass, Glenn R.; Simoneit, Bernd R.T., "Source apportionment of airborne particulate matter
using organic compounds as tracers, "Atmospheric Environment, Vol. 30, 1996, No. 22, pp.
3837-3855,.

       2As described in Cadle, Steven H.; Gorse, Robert A.; Belian, Timothy C.; Lawson,
Douglas R., 1993, "Real-world vehicle emissions:  A Summary of the Eighth Coordinating
Research Council On-Road Vehicle Emissions Workshop", Journal of the Air and Waste
Management Association, v.49, p.242-255.

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must acknowledge this omission, since neglect of the mobile source  contribution results in a
potentially large underestimate of the benefits of reducing directly emitted PM.

       This emissions inventory issue could distort the air quality simulations. The study
Appendix C states on page 45, that the Regional Acid Deposition Model-Regional Particulate
Matter (RADM-RPM) organic aerosol estimates were not included in the final analysis because
the model significantly underestimated organics and the reason for this systematic
underestimation has not yet been characterized.  These underestimates can be attributed to
limitations in the model formulation and to input emissions and meteorological data. We suggest
that one major reason for this underestimation is that most organic material appears to be directly
emitted and that it is underestimated by several fold in the inventories used in the 812
Prospective Study and the national emission trends inventories.

       The AQMS has another concern with the PM emissions estimates that has a direct impact
on the quality of the air quality modeling results to be used in the cost/benefit analysis. The
comparison of the PM 10 estimates in the Regulatory Modeling System for Aerosols and
Deposition (REMSAD) with measured values in the western United States show a  pattern of
substantial underestimation. Because this pattern is much more prevalent for PM 10 than for PM
2.5, it suggests that the sources are more localized in their effects on airborne concentrations than
the size of the modeling grid cells.  Thus, averaging over the whole volume of the modeling grid
cell leads to consistent underestimation in the PM concentrations. This raises a problem for the
estimation of concentrations at the census tract level.  If the effects of the PM are  linear with no
threshold, then there should not be a problem with the assumptions in the analysis.  However, if
there is a threshold and a non-uniform distribution of population across the grid cell, there could
be substantial under or overestimation of effects. It is not feasible to eliminate this problem in
the current Prospective Study, but it needs to be recognized as a potentially large source of
uncertainty in the outcome.

       Charge Question 5: The Project Team has used an expanded array of air quality model-
derived adjustment factors to estimate changes relative to baseline air quality concentrations.
Specifically, rather than a single adjustment factor applied in the Retrospective Study to estimate
concentration changes across the entire range of initial ambient concentrations for a given
pollutant,  ten separate adjustment factors were calculated and applied based  on decile midpoints
generated by the relevant air quality model. Do the Council and AQMS consider this
methodological change to reflect an improvement in the validity  and reliability of projected
concentration changes?

       Response. The proposal to derive separate adjustment factors for different concentration
ranges from results of the model and then to apply the factors to observations to obtain future
changes in air quality seems reasonable. The choice of percentile values at which to make the
changes in an adjustment factor also seems to be justifiable.  To demonstrate the validity of the
approach, we recommend that the Agency show illustrations of the observed distributions and
the simulated distributions so that the two distributions can be easily compared.

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       Charge Question 6: The Project Team has used an alternative spatial inte  rpolation
method to estimate baseline air quality concentrations in locations that do not have adequate
local monitoring data.  In the Retrospective Study, complete representation of initial air quality
conditions in the 48 contiguous states for each pollutant was obtained by simple spatial
interpolation to each unmonitored or under monitored location from the closest relevant,
sufficiently operated monitor.  Based on advice from the AQMS and Council pursuant to the
January - February 1998 review meetings, the Project Team sought to develop an enhanced
methodology based on a space-time continuum concept described by the AQMS.  The homology
mapping technique subsequently developed by the Project Team proved promising in initial
validation tests; however the Project Team concluded that additional development and validation
work should be completed before using the tool in the context of the section 812 studies.  As an
alternative, an enhanced version of the traditional spatial interpolation method was developed
which relies on inverse distance-weighted interpolation from multiple surrounding monitors. This
technique is referred to as Voronoi Neighbor Averaging (VNA). The Project Team requests
advice from the Council and AQMS on the two sub-questions:

       Charge Question 6.1. Do the Council and AQMS consider the homology mapping
technique a reasonable adaptation of the space-time continuum concept previously advanced? If
so, what specific additional development, testing, and validation steps do the Council and AQMS
recommend be undertaken by the Project Team to facilitate potential use of this technique in
future assessments?

       Charge Question 6.2. Do the Council and AQMS consider the change to the  VNA
approach to reflect an improvement in the validity and reliability of projected initial air quality
concentration estimates relative to the previous, single  monitor spatial interpolation method?

       Responses. The use of the VNA method is reasonable and justifiable for interpolating
within the bounds of a region surrounded by monitors.  It is much less certain that it can be used
to extrapolate over substantial distances where no data are available. The homology mapping
technique appears promising, but it would be premature to employ it in this Prospective Study
without further refinement of the input data and testing.

       The need for a technique like VNA arises from  the basic approach as shown in Figure II-
1, p. 2-4 of the Technical Report. Because model-derived adjustment factors are applied to
measurement data, the approach is limited to those locations that have observatories.  Due to the
request from the Council to provide complete coverage of forty-eight states and because  only
81% of the population live in counties within 50 kilometers of a monitor, there arises a need to
estimate ozone and PM distributions for the non-monitored counties. In the Retrospective Study,
these estimated counties were assigned the same values as the nearest monitored location.

       In response to advice from the AQMS, the Agency sought to improve upon this process
and has produced two techniques, the VNA method and the homology mapping technique. While
the VNA method does a better job of interpolation than simply assigning the nearest monitor,
interpolation of a sparse, highly variable field may not be appropriate. This is because no process

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or cause-and-effect information that spans the non-monitored area was used in the VNA
algorithm and the VNA method merely computes a surface at the average height of the nearest
monitors (effectively VNA interpolates the results, not the causes). When nearest monitors are
located in different causal regions linearly interpolating between those regions may produce very
serious errors.  For example, between Columbia, South Carolina; Atlanta, Georgia; Jacksonville,
Florida; and Tampa Florida, the VNA method produces a nearly uniform field of ozone at the
average value of the monitors in these four cities, more than 120 ppb, yet the air quality model
shows that there is an ozone minimum between Atlanta and Jacksonville that is 60 ppb for one
case and 40 ppb (the model's background) on other days.  This type of problem happens in Texas
and between Portland, Oregon and Seattle, Washington. The Agency also developed another
methodology, the homology mapping technique which assumes  that similar features or
characteristics result in similar ozone or PM. This is not an interpolation method; it is a
substitution method. It assumes that the monitored data set has a set of conditions that are
sufficiently similar to those in the non-monitored regions and that there is a set of discriminating
features available for both the monitored and non-monitored areas. This method is more causally
dependent than the VNA method and potentially more accurate than the VNA method.
Successful application of the method depends on the selection of a feature set that is truly causal
for the phenomenon being estimated.

       The AQMS concurs with the Agency that application of the homology mapping technique
is premature given its stage of development and testing.  The AQMS believes that this method
has sufficient promise that it should be further developed and evaluated. This includes exploring
alternative feature sets such as, for example, adding terrain (e.g., valley floor, mountain side), use
of neural-net techniques, and extensive testing within the data set.

       As presently formulated, neither the VNA nor the homology mapping technique takes
advantage of the best cause and effect relationships available to the Agency, the air quality
model simulations themselves. A lot of effort was expended to produce 48-state model coverage,
but the choice  of model scaling technique, which requires monitored data, results in the loss of
important information contained in the model output. The AQMS gave the Agency oral advice in
May to develop a method that would take advantage of the air quality  modeling simulation
results in estimating concentrations at the  non-monitored counties.

       The Subcommittee received a proposal for just such a method immediately before the
June 3, 1999 teleconference call.Although the proposed method is not  tested, the Subcommittee
finds it an acceptable approach for the current Prospective Study, provided the Agency
acknowledges that the modified VNA method depends in part on simulation models.  As a result,
it will be subject to the uncertainties associated with them.  Acknowledgment of these model-
related uncertainties needs to appear both in the discussion of the VNA approach. It also needs
to be reflected in the discussion of overall sources of possible error in the estimated health and
ecological effects which are based on the air quality analysis results.

       The AQMS also suggests that the Agency develop a testing protocol that compares the
VNA method for two different sets of locations, those near monitors and those more  distant from

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monitors.  The results from this test will help guide the design of future Prospective Studies. In
future studies, the homology mapping technique should be further developed and alternative
feature sets should be explored, perhaps including county-averaged emission density.

Conclusion

       In summary, the AQMS commends the study team on the progress since the last review.
The remaining limitations (particularly those associated with the PM emissions and air quality
simulations), if captured in concise discussions and tables, should strengthen the acceptability of
the overall report.  We  also want to emphasize that future prospective studies could benefit
greatly from our recommended Agency-wide analysis of representativeness and reliability of
emissions modeling, use of the same, high quality air quality modeling system platform (such as
Models-3) across the entire United States, and further exploration of a wider range of techniques
for dealing with uncertainties in complex assessments.  The AQMS is ready to help support the
emissions review and reconciliation of emissions inventories and modeling results with
observations. This issue cuts across many activities of the Agency and deserves careful
consideration.

       We thank the Agency for the opportunity to be of service in review of the building blocks
that will lead to the forthcoming Prospective Study and to the review of the draft Study itself.
We look forward to the response to this Advisory from the Assistant Administrator of the  Office
of Air and Radiation.
                                  Sincerely,
       Dr. Maureen L. Cropper, Chair             Dr. Paulette Middleton, Chair
       Advisory Council on Clean Air             Air Quality Models Subcommittee
        Compliance Analysis                     Advisory Council on Clean Air
                                                 Compliance Analysis

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                 U.S. ENVIRONMENTAL PROTECTION AGENCY
                       SCIENCE ADVISORY BOARD (SAB)
           ADVISORY COUNCIL ON CLEAN AIR COMPLIANCE ANALYSIS
                                   (THE COUNCIL)

CHAIR
Dr. Maureen L. Cropper, The World Bank, Washington, DC

MEMBERS
Dr. Gardner M. Brown, University of Washington, Seattle, WA

Dr. A. Myrick Freeman, Bowdoin College, ME

Dr. Don Fullerton, University of Texas, Austin, TX

Dr. Lawrence H. Goulder, Stanford University, Stanford, CA

Dr. Jane V. Hall, California State University, Fullerton, CA

Dr. Charles Kolstad, University of California, Santa Barbara, C A

Dr. Paul Lioy, Robert Wood Johnson School of Medicine, Piscataway, NJ

Dr. Paulette Middleton, RAND Center for Science & Policy, Boulder, CO

CONSULTANTS
Dr. Alan J. Krupnick, Resources for the Future, Washington, DC

SAB COMMITTEE LIAISONS
Dr. William H. Smith (EPEC), Yale University, New Haven, CT

SCIENCE ADVISORY BOARD STAFF
Dr. Angela Nugent, Designated Federal Officer, Science Advisory Board, US Environmental
      Protection Agency, Washington, DC

Mrs. Diana L. Pozun, Management Assistant, Science Advisory Board, US Environmental
      Protection Agency, Washington, DC

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                   U.S. ENVIRONMENTAL PROTECTION AGENCY
                             SCIENCE ADVISORY BOARD
           ADVISORY COUNCIL ON CLEAN AIR COMPLIANCE ANALYSIS
                                   (THE COUNCIL)
                      AIR QUALITY MODELS SUBCOMMITTEE

CHAIR
Dr. Paulette Middleton, Science Policy Associates, Boudler, CO

MEMBERS
Dr. Philip Hopke, Clarkson University, Dept. Of Chemistry, Pottsdam, NY

Dr. Harvey Jeffries, Dept. of Env. Sciences & Engineering, University of North Carolina, School of
      Public Health, Chapel Hill, NC

Dr. Timothy V. Larson, University of Washington, Seattle, WA

Dr. Peter K. Mueller, Electric Power Research Institute, Palo Alto, CA

Dr. James H. Price, Jr., Texas Natural Resource Conservation Commission, Austin, TX

Dr. George T. Wolff, General Motors Environmental & Energy Staff, Detroit, MI

SCIENCE ADVISORY BOARD STAFF
Dr. Angela Nugent, Designated Federal Officer, Science Advisory Board, US Environmental
      Protection Agency, Washington, DC

Mrs. Diana L. Pozun, Management Assistant, Science Advisory Board, US Environmental
      Protection Agency, Washington, DC

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                                         NOTICE
       This report has been written as part of the activities of the Science Advisory Board, a public
advisory group providing extramural scientific information and advice to the Administrator and other
officials of the Environmental Protection Agency. The Board is structured to provide balanced,
expert assessment of scientific matters related to problems facing the Agency.  This report has not
been reviewed for approval by the Agency and, hence, the contents of this report do not necessarily
represent the views and policies of the Environmental Protection Agency, nor of other agencies in the
Executive Branch of the Federal government, nor does mention of trade names or commercial
products constitute a recommendation for use.
Distribution and Availability: This Science Advisory Board report is provided to the EPA
Administrator, senior Agency management, appropriate program staff, interested members of the
public, and is posted on the SAB website (www.epa.gov/sab). Information on its availability is also
provided in the SAB's monthly newsletter (Happenings at the Science Advisory Board). Additional
copies and further information are available from the SAB Staff.
                                             in

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                     GLOSSARY OF TERMS AND ACRONYMS
ADV
AQMS
CAAA
C-R
EPA
GIS
HAP
HEES
LTR
N
PM
PM25
PM10
ppb
RADM-RPM
REMSAD
VNA
       Advisory
Air Quality Models Subcommittee (of the Council)
Clean Air Act Amendments
       Concentration-Response
       U.S. Environmental Protection Agency (U.S. EPA)
       Geographic Information System
       Hazardous Air Pollutant
       Health and Ecological Effects Subcommittee (of the Council)
       Letter Report
       Nitrogen
       Particulate Matter
       Particulate Matter (2.5 microns in diameter)
       Particulate Matter (10 microns in diameter)
       Parts per billion
       Regional Acid Deposition Model-Regional Particulate Matter
       Regulatory Modeling System for Aerosols and Deposition
       Voronoi Neighbor Averaging
                                            IV

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