REPORT OF THE
  REVIEW PANEL ON TOTAL HUMAN EXPOSURE
REVIEW OF THE AGENCY'S ONGOING RESEARCH
IN UNDERSTANDING TOTAL HUMAN EXPOSURE TO
    INDOOR AND AMBIENT AIR POLLUTION-'
  U.S. Environmental Protection Agency
         Science Advisory Board
         Washington, D.C. 20460
               May   1985

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                               NOTICE
     This report  has been  written  as  part  of  the  activities  of  the
Environmental Protection  Agency's  Congressionally established  Science
Advisory Board, a public group providing extramural advice on scientific
issues.  The  Board  is  structured  to  provide a  balanced,  independent,
expert assessment  of  scientific  issues  it  reviews,   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.

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                              TABLE OF CONTENTS
                                                                       PAGE

  I.   EXECUTIVE SUMMARY  	    1


 II.   INTRODUCTION	    3


III.   REPORT ON THE PROGRAM REVIEW ON TOTAL HUMAN EXPOSURE 	    4

       A.  Background and Limitations of This Review  	    4
       B.  Overview of Exposure Assessment Needs
             Within the EPA	    5
       C.  Review of Current EPA Programs	    7

              1.  Program Management	    7
              2.  Research Activities 	 	    8
              3.  Additional Issues Not Currently Being
                    Addressed 	    9

       D.  Reviews of Specific EPA Programs	   12

              1.  Instrumentation	   12
              2.  Field Studies	   12
              3.  Modeling	   15
              4.  Dosage Research	   16


 IV.   APPENDICES

       A*  Charge to the Review Panel	   A-l

       B.  Roster of the Review Panel	   B-l
                                  ii

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                             Key to Acronyms
EMTS




EPA




MEM




NAAQS




NEM




N02




OAQPS




ORD




PEM




SAB




SALTRP




SHAPE




TEAM




voc
Exposure Methods Test Site




Environmental Protection Agency




Microenvironmental Monitoring




National Ambient Air Quality Standards




NAAQS Exposure Model




Nitrogen Dioxide




Office of Air Quality Planning and Standards




Office of Research and Development




Personal Exposure Monitoring




Science Advisory Board



Strategic and Long-Term Research Planning (Subcommittee)




Simulated Human Air Pollution Exposure




Total Exposure Assessment Methodology




Volatile Organic Compound
                                   iii

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I.   EXECUTIVE SUMMARY
     This is the report of the Science Advisory Board's  (SAB) Total Human
Exposure Review Panel.  The Panel met on February 25-26, 1985 at EPA's
Environmental Research Center, Research Triangle Park, NC, in order to
review the Agency's research program on total human exposure to indoor
and ambient air pollution.

     The Review Panel focused on five major topic areas  described in the
program document prepared by the Office of Research and  Development:
1) development of measurement methods; 2) statistical protocols, data-base
development, and exposure models; 3) microenvironmental  field studies;
4) total human exposure field studies; and 5) dosage research investigations,
This program document was well organized, informative, and provided the
Panel with an excellent means to focus their questions and discussion.

     The Review Panel was impressed with the quality of  the scientific
effort being expended by Agency staff scientists.  It was clear to the
Panel that certain dedicated professionals have recognized the importance
of this issue and have carried out research of high scientific quality
to improve our understanding of total human exposure.  While the Panel
recognizes this laudable effort, it also notes that the  level of support
for this effort is less than it should be.  The criticisms noted in this
report should be taken as the Panel's effort to help the Agency improve
the total human exposure program.

     Based on a review of the Agency's program document  and the presenta-
tions made at the meeting, the Panel has three major recommendations.
These are that the Agency:

     •   Identify the issue of total human exposure as an emerging
         scientific issue of critical importance to the  Agency's
         responsibilities;

     •   Coordinate future research activities related to total
         human exposure at senior levels of the Agency;  and

     •   Base future data collection activities on carefully developed
         experimental design and probability sampling protocols.

     The Panel has organized its overall findings into three areas.
These are: 1) program management; 2) research activities; and 3) areas
of research not currently being performed.

     The overall objectives, mandate, organizational structure, and
level of support of the Total Human Exposure Program were not clearly
stated during the presentations.  There also appeared to be no strategic
planning, coordination or organized direction of this program from senior
levels of the Agency.  The technical work is generally excellent but the
significance, cost effectiveness, and ultimate regulatory impact is so
far-reaching that the EPA management should pursue the program with far
more emphasis and central leadership than it currently receives.

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     The Panel recommends that the exposure assessment activities within
the Agency have a.central management and administration such that activities
in the required technical areas (development of instrumentation, field
studies, modeling, and health effects) are thoughtfully integrated.  This
project integration can only be accomplished effectively by coordination
among the EPA Research Committees and project officers at the highest
levels within the Agency.  This focus and concept of a strategy must be
formalized into a commitment by senior EPA management to understand
total human exposure to pollutants and its relationship to sources, doses,
toxicity, and the protection of public health.

     The Agency's ability to perform credible quantitative risk assessments
is severely constrained by the limitations in current capabilities in
exposure assessment.  Although much of the progress in exposure assessment
technology that has taken place in recent years was supported by the
EPA, the level of support from the Office of Research and Development
(ORD), as well as from the program offices has been limited in terms of absolute
dollars invested.

     The Panel recommends that future advances in the Agency's capabilities
for total human exposure assessments should be built on its past accomplish-
ments.  In particular, the Panel refers to the pioneering and successful
major field studies represented by the Total Exposure Assessment Methodology
(TEAM) Study and the Denver, CO and Washington, DC carbon monoxide exposure
field studies.  The results of these studies can help guide the Agency's
approach to environmental monitoring, assessment, and regulation of air
pollutants.  In addition, work needs to be done on other pollutants
besides carbon monoxide.

     In reviewing specific research programs, the Panel had several
observations:  1) Instrumentation - The Panel recognizes the importance
of instrument and method development in meeting the needs of exposure
assessment; the current EPA work is very good, however, this effort is
not sufficiently comprehensive at the existing level to meet the needs of
the field studies.  Moreover, the reliance on passive and active sorbent
devices should be complemented by other sampling schemes such as sensor
arrays, fiber optic devices, solid-state transducers, and electrochemical
sensors.  2) Field Studies - The EPA staff are to be commended for their
scientific contributions to development of the indirect and direct approaches
to exposure assessment, and for their early recognition of the critical
role of survey sampling methodology in development of valued exposure
assessments.  In addition, the Panel applauds EPA's efforts in conducting
the TEAM Study and recommends that comprehensive exposure studies of this
type be continued and expanded to other pollutants and additional locations.
3) Modeling - The Panel endorses the plan to validate the SHAPE (Simulated
Human Air Pollution Exposure) model with actual field data, and the
effort to validate and modify the National Ambient Air Quality Standard
(NAAQS) Exposure Model (NEM) to accept empirical activity data as input.
Such validation would enhance the use of those models in future studies.
4) Dosage Research - Although the Panel's review of this program was
brief, it was apparent that the work being done in this area was reasonable
and productive.  However, it was clear that dosage research was not being
conducted in connection with exposure research.  The Panel views this as
a weakness since a coordinated health component is important to the
exposure assessment activity.

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     The Panel has developed a set of issues that the Agency should  con-
sider in defining its research agenda for future human exposure assessments,
These include:

     1)  further efforts in understanding human exposure to nitrogen
         dioxide and size-fractionated particulate matter;

     2)  exposure studies should be undertaken for other criteria
         pollutants;

     3)  a coordinated effort should be undertaken to develop the
         tools and methods required for these exposure assessment
         activities;

     4)  residential and commercial applications of pesticides and
         termiticides represent an important potential source of
         inhaled or ingested exposure; and

     5)  exposure studies and health assessments should be more
         carefully coordinated.
II.  INTRODUCTION
     At  the request of  the Agency's Office of Research and Development,
the Science Advisory Board has agreed to conduct a series of one-time
reviews  on a number of  ongoing research programs within the Agency.  The
reviews  will be coordinated under  the auspices of the SAB's Subcommittee
on Strategic and Long-Term Research Planning (SALTRP).  The purpose of
these reviews is to conduct a peer review of an ongoing research program
by a review panel  of recogized experts in order to communicate to the
Agency the progress, or lack of progress being made in meeting research
needs pertinent to the  development of Agency regulations and policy.

     Each review will be conducted by a different review panel and will
take place at an appropriate laboratory or other location where the
panel will receive briefings and prepare its report.  Approximately
two reviews will take place each calender quarter.  Once a review is
completed, the chairperson of each review panel will brief the Deputy
Administrator on the findings and  recommendations of that panel.

     The Review Panel on Total Human Exposure was charged with the task of
advising the Agency on  how well the research program for Total Human
Exposure is progressing toward answering the needs of the Agency, including
both whether or not the right research is being conducted to address
issues defined by  the Research Committee process, and whether the research
is being conducted properly.

     This report presents the results of the first program review in
this series:  The  Review of the Total Human Exposure Program.

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III.   REPORT OF THE PROGRAM REVIEW ON TOTAL HUMAN EXPOSURE

       A.  Background and Limitations of This Review


       This is the report of the Science Advisory Board's Total Human
Exposure Review Panel which met on February 25-26, 1985 in Research
Triangle Park, North Carolina.   On the first day the Panel received
briefings, allowing EPA project managers and scientists to present the
highlights of the Total Human Exposure Program.  On the second day the
Panel prepared the present report.

     The Panel found the material presented to  be both interesting and
useful.  This review was a first, both for the  Panel members and EPA
staff.  There were, inevitably, a number of informational areas, mostly
of  a non-scientific nature,  that were not presented and which would have
been useful, in fact necessary, for  the Panel to make a clear assessment
of  the  overall merits  of the program.  Some of  these areas were:


     •   The overall objectives of  the program  were not clearly
         delineated, and some  of  the  scientific presentations did not
         discuss  the hypothesis being  tested.

     •   There were no cost  or effort  estimates of the entire program or
         its  specific  components.   This made  reviewer's curious  about the
         emphasis placed on  each  program component and its cost-effectiveness,

     •   No  attempt was made to  elucidate  the mandate  for  the program,
         its  organizational  structure within  the EPA,  or the chain of
          command  of  the staff  involved.

     •    In  many  cases staff did  not discuss  their future  plans  for
          continuation  of  their projects,  or if  they  did not  expect  to
          continue, why not.

      •   There was no  discussion of other EPA projects that,  at  least
          to  some  degree,  could be termed  Total  Human Exposure Assessments,
          or why there was  not  more integration with  these  projects.

      •    The charge to the Panel with respect to  the report  was  not
          adequately expressed, either formally or informally.


      On a  positive note,  the Panel was pleased with  the content  of the
 scientific presentations,  the manner of presentations, and the fact that
 the scientific format was  geared to the Panel's needs. The research
 summaries  delivered to the Panel prior to the meeting were well organized
 and informative.   Clearly the staff involved in the  total assessment program
 is of  very high caliber.   The Panel was pleased with the flexibility
 displayed by EPA staff when requested to substantially alter the afternoon's
 proceedings, at some inconvenience to individual staff.

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     The criticisms discussed above should not reflect on the EPA staff
or the Panel members so much as on the newness of this particular review
process.  The Panel recommends that, for future reviews, the Panel chair-
person be responsible for consulting with Agency staff prior to the meet-
ing in order to set the agenda and format, taking into account the items
discussed above.  Whenever possible, the formats of the presentations
of the individual scientists should follow, within reason, a standard
format, including hypothesis, methods, cost, results, technical problems
and future plans.

     The Panel trusts that the criticisms made above will not detract
from its general view of the merits of the program or of the excellent
scientific base developed thus far.
     B.  Overview of Exposure Assessment Needs Within EPA
     Based on its review of  the Agency's research program on Total Human
Exposure, the following represents the Review Panel's overall conclusions
and overview of EPA's programmatic needs.

     The EPA's ability to perform credible quantitative risk assessments
is severely constrained by the limitations in current capabilities in
exposure assessment.   Recent research has demonstrated that individual
exposure to criteria air pollutants is strongly influenced by indoor
environments.  The contribution of gas cooking stoves to personal exposure
to nitrogen dioxide is one dramatic example, but indoor sources and sinks
modify exposure to all air pollutants.  Recent work by EPA scientists has
shown that indoor sources are equally important for volatile organic
compounds (VOC).  Better understanding of total human exposure to air
pollutants is critical to the long-term effectiveness of EPA's regulatory
strategy, to the choice of margins of safety to ambient standards, to
the identification of high-risk populations, and to future epidemiologic
research.

     In another setting, a recent study by the National Academy of Sciences
on Toxicity Testing Needs found that the toxicity data base was inadequate
for toxicity evaluation for  50% of pesticides and 88% of chemicals in
commerce.  The Academy recommended that priorities for further testing should
be guided by the potential for human exposure, for which the data base
was even more inadequate than for toxicity.  For toxicity testing, there
may be inadequate data for most chemicals, but there is at least general
agreement on how the tests should be performed.  The science of exposure
assessment is less well developed, especially for general population
exposures.

     Much of the progress in exposure assessment technology that has
taken place in recent years  was supported by EPA.  However the level of
support from the Agency's Office of Research and Development (ORD) and
the program offices has been limited, and in its aggregate the level of
effort has been too meager to permit advances in capability commensurate
with the needs for increased numbers of ever more sophisticated risk

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assessments.  While each program office has specific needs in exposure
assessment technology, they also share some generic needs with each
other and the ORD.  Therefore, it is in their best interests to support a
research program focused on improvements in exposure assessment technology,
Such a program should be carried out by the ORD, in cooperation with
appropriate program office personnel, for several reasons.  First, the
ORD has personnel with much valuable insight and experience on these
issues and is familiar with the needs of the program offices.  Second,
none of the individual program offices is likely to invest in research
which is not closely tied to immediate program needs.

     Future advances in the EPA's capabilities for total human exposure
assessments can, and should, be built on its past accomplishments.  Among
these are the pioneering and successful major studies represented by the
TEAM (Total Exposure Assessment Methodology) Study and the Denver and
Washington, D.C. carbon monoxide exposure field studies.

     The results of these studies can help guide the Agency's approach
to environmental monitoring, assessment, and regulation of air pollutants.
The issues these studies raise include:
     •  What should be  the Agency's regulatory stance toward indoor exposure?
        Even if the Agency were  to take the position that it has no
        regulatory role  in indoor environments, it must recognize in
        its approach  to  assessment and regulation that indoor exposures
        are often greater than outdoor exposures.

     •  The emerging  information about the indoor environment raises
        doubts about  the adequacy and, for the same pollutants, even
        the relevance,  of outdoor monitoring for protection of public
        health.

     •  To assess the importance of sources and the amount of a dose,
        exposures must  be characterized.

     •  What advances in measurement  technology are needed for future
        studies?


On a more operational level,  other questions arise:


     •  Are current and planned  expenditures for total human exposure
        assessment consistent with the Agency's information needs for
        assessment and  regulation?

     •  What level of precision  of exposure information is appropriate
        in different  research and regulatory settings?

     •  How should monitoring resources be allocated between studies
        of exposure distributions and monitoring activities in support
        of epidemiologic research?

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To address these issues, the Panel  recommends  that  the Agency:
     •  Identify the issue of  total human  exposure  as  an  emerging
        scientific  issue  of  critical  importance  to  the Agency's
        responsibilities;

     •  Coordinate  future research activities  related  to  total human
        exposure at senior levels of  the Agency;  and

     •  Base future data  collection activities on carefully  developed
        experimental design  and  probability  sampling protocols.
     C.  Review of  Current  EPA Programs

         1. Program Management


     The presentations  to  the Review Panel  by EPA management  and  staff
 scientists  reflected  the view that  total  exposure assessment  is required
 in  order to perform credible risk assessments and, ultimately, to perform
 the regulatory functions of EPA.  The Review Panel agrees with this
 concept.  Moreover, the individual  presentations  made  it  clear that
 several dedicated professionals within the  Agency have recognized the
 importance  of  this  issue and have carried out research of high scientific
 quality to  improve  our  understanding of  total human exposure..  Important
 findings have  been  reported that  can affect both  exposure assessment and
 the EPA's regulatory  policies of  the future.  It  was also clear,  however,
 that there  is  no strategic planning, coordination, or  organized direction
 of  this total  human exposure assessment  activity  from  senior  levels of
 the Agency. The technical work is  generally excellent but  the significance,
 cost-effectiveness, and ultimate  regulatory impact is  so  far-reaching
 that,  in the Panel's  opinion, EPA management should pursue  the program
 with far more  emphasis  and central  leadership than it  currently receives.

       The Panel recommends that the exposure assessment activities within
 EPA have a  central  management and administration  such  that  activities in
 the required technical  areas (development of instrumentation, field
 studies, modeling,  and  health effects) are  thoughtfully integrated.
 Further, the exposure assessment  activities should be  linked  to the
 overall risk assessment model presented,  i.e., to sources and to  the
 dose/toxicity  assessment activities.

      This project integration can only be accomplished effectively by
 coordination among  the  EPA Research Committees and project  officers  at  the
 highest levels within the  Agency.  This focus and concept of  a  strategy
 must be formalized  into a  committment by senior EPA management  to under-
 stand  total human exposure to pollutants and its  relationship to
 sources, doses, toxicity,  and the protection of the public  health.

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         2.  Research Activities
     Of the many components  that  relate  to  an  overall  risk assessment  for
any particular chemical, many, but certainly not all,  were presented to
the Review Panel.  The overall focus of  the research activities presented
was on exposure assessment,  but there was also some discussion of dosage
assessment,  Dosage assessment activities,  however, do not appear to be
coordinated with any of the  exposure assessment activities.

     Agency scientists have  made  significant progress  in developing the
conceptual approach and methodology for  determination  of total human
exposure to pollutants.  Basically, two  procedures have been suggested
and actually implemented on  a limited scale.   The first is the concept
of personal exposure monitoring (PEM).   This requires  that a small
measuring device actually be worn by subjects  as they  go about their
normal activities.  The second concept is that of microenvironmental
monitoring (MEM), which requires  the measurement of a  pollutant's
concentration in a variety of locations  inhabited by people during a
normal day's activity and a  reconstruction  of  a complete exposure history
by combining these measurements with an  activity log.  The two methods
should yield comparable results if each  is  performed properly.  As yet,
comparable results have not  been  achieved.  For example, exposure estimates
differ by about forty percent for the Washington, D.C., carbon monoxide
study.

     The EPA has a substantial program in the  development of measurement
methods for assessing total  human exposure, although most of this activity
is clearly funded by the base research and  development program.  Most of
the research presented to the Panel was  concerned with the measurement
of volatile and semi-volatile hydrocarbons, either by  means of a personal
exposure monitor or by means of a larger sampler suitable for micro-
environmental monitoring.  Although there is a major expenditure in
developing a sensor for nitrogen  dioxide and some effort in developing a
sampler to measure volatile  organic compounds  that are associated with
particles of diameter less than lOjum, there is very little activity in
developing instrumentation for the measurement of other pollutants.

     Several field studies have been conducted in the  past by the EPA.
Two of these were related to exposures to carbon monoxide and have been
essentially completed and reported.  Another study, the Total Exposure
Assessment Methodology (TEAM) study was  presented in detail.  This study
is examining exposure to airborne volatile  organic pollutants in several
locations over time periods  long  enough  to  establish temporal patterns.
The results, as they define  sources of exposure to organic chemicals,
are most provocative and indicate that "traditional" sources of exposure
may be minor compared to other more "personal" sources.  This study,
more than any other, provides compelling evidence of the necessity of
evaluating total human exposure and of not  basing exposure estimates on
pollutant concentrations measured only by fixed station monitors.

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     Finally, some material on  dosage  evaluation was  presented  to  the
Panel.  Most of the time was devoted to  a  study in China  that seeks  to
explain the very high  incidence of  lung  cancer in a small region.  Other
material of a diffuse  and general nature was  presented, but  it  was fairly
clear that there is no dosage-research study  that is  connected  with  the
exposure-research study.  The Review Panel views this  as  a weakness
since a coordinated health component is  important to  this exposure assess-
ment activity.  The present health-component  would need significant
redirection in order to complement  the exposure studies reviewed here.
         3.  Additional  Issues Not  Currently  Being Addressed
     As discussed  above,  the  current  "Total Human Exposure  to Air Pollutants"
program within  the EPA has  been  limited  in scope.  Human exposures have been
examined for  only  a  few  pollutants.   These projects were primarily directed
toward deriving a  frequency distribution of exposures  in a  representative
population.   The relevancy  to other useful applications of  exposure assess-
ments was not explicitly considered,  although  further  data  analysis will
greatly enhance their usefulness.  Further, the  biological  and health related
endpoints of  the EPA's exposure  assessment work  are not well characterized,
are limited primarily to mutagenicity, and are not an  integral part of the
field and laboratory studies.

     This section  sets forth  a set of issues that the  Agency should con-
sider in defining  its research agenda for future human exposure assessments.
This research should help to  quantify population exposure,  identify the
portion of the  population at  greatest risk, and  identify determinants of
exposure (including  specific  sources, locations, and activity patterns).
When linked to  health studies, human  exposure  studies  can assist in the
quantification  of  potency factors for a  variety  of hazardous substances
and air contaminants.


     a.   Nitrogen Dioxide  (NO?) - Studies have  demonstrated the import-
          ance  of  unvented  combustion sources  (mostly  in homes) to inte-
          grated and peak N02 indoor  concentrations.   Limited personal
          monitoring has identified the  importance of  these indoor sources
          as  contributors to  total human exposure, but these studies did
          not utilize probability sampling in  selecting participants or
          monitoring plans.  Health endpoints  were not examined concurrent-
          ly  with  exposures.   Actual  peak exposures are not well-document-
          ed  and will not be  until instrumentation is  improved.  The EPA
          has a direct interest  in understanding human exposures to N02
          in  order to provide improved estimates of health  effects and to
          properly restructure air quality standards.

     b.   Particles  - Human exposures to particulate matter is a vexing
          problem.  Indoor  concentrations are  an important  contributor
          to  the integrated exposures to respirable size particles.

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However, the size'distribution,  chemical composition, and,
quite likely, general toxicity of indoor particulate matter
will differ from that of outdoor particles.  The Agency needs
to understand human exposures to size-fractionated particulate
matter from the perspective of source contributions and by
fractional components.  Fractional components will have different
toxicological effects.  The relevant issues include:
1)   Characterizing acute integrated exposures to acid aerosols;
     The covariance of outdoor activities and acid events
     should be examined.  The penetration of acid aerosols
     into indoor environments, the neutralization of acid
     aerosols indoors and the generation of acid gases and particles
     indoors could be additional area of inquiry.  Panel members
     disagreed about the importance and cost-effectiveness of
     research on these issues.

2)   Characterizing human exposure to vehicle exhaust;  Receptor
     modeling of urban aerosols has identified vehicle exhaust
     as a ubiquitous contributor to ambient particulate matter.
     Limited in-vehicle studies have demonstrated several-fold
     higher concentrations than measured at :fixed sites.   Al-
     though in-transit time may be only 5 to 10% of an individual's
     daily activities, this may represent an important exposure
     opportunity for specific compounds and metals.

3)   Characterizing human exposure to fossil and biomass fuel
     related primary emissions;  It will be important to quantify
     the amount and location of human exposure to combustion
     derived particulate matter.  The emphasis should be on
     condensible organic fractions and a few metals (e.g. arsenic,
     vanadium, selenium).

4)   Characterizing human exposures to cigarette smoke;  Passive
     smoke exposure occurs predominantly indoors.  Respiratory
     health effects, including cancer, are either documented or
     suspected to be associated with exposure to passive smoke.
     Discerning possible health effects associated with other
     components of respirable particulate matter will require
     careful separation of the possible passive tobacco smoke
     effects.  Therefore, an exposure assessment program should
     utilize appropriate markers for tobacco smoke in character-
     izing exposures to segments of our population.  This might
     be an> area where microenvironment sampling is an appropriate
     approach.

5)   Characterizing asbestos fiber exposures;  While friable
     asbestos insulation material has been noted in schools,
     offices and homes, an understanding of actual airborne
     concentrations of asbestos fibers is missing.  To undertake
     appropriate risk assessment and to determine remedial
     actions, better information on either environmental
                          10

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          concentrations of, or personal exposures to asbestos fibers
          is needed.  These studies should be longitudinal because of
          the episodic nature of fiber release.  They should include
          residential locations.
£•   Exposure studies should be undertaken for other criteria
     pollutants - The emerging evidence on the importance of indoor
     environments and personal activities to air pollution exposure
     suggests that current approaches to air pollutant regulation
     based on outdoor measurements may become less defensible in
     the near future.  The importance of total human exposure assessment
     should be reviewed for each criteria pollutant to identify
     those for which integrated exposure assessment is most urgently
     needed.

d.   A coordinated effort should be undertaken to develop the tools
     and methods required for these exposure measurement activities.

e.   Residential and commercial applications of pesticides and
     termiticides represent an important potential source of inhaled
     or ingested exposure - The Agency should undertake a carefully
     designed study (i.e., such as TEAM) of human exposures to
     halogenated compounds and to quantify the sources and routes
     of exposure.

f.   Exposure studies and health assessments should be more carefully
     coordinated - These two components do not necessarily have
     to be integrated into every study.  However, the relevance
     of the health related research to actual human exposures should
     be explicit.   For example, the mutagenicity work currently
     associated with the indoor air pollution research program, and
     identified as a component of the total human exposure program,
     could be better integrated into measurement and risk assessment
     activities.  Because of the cost and time involved in conducting
     multi-dose bioassys with pollution mixtures, carefully designed
     sampling schemes should be employed.  Environmental conditions
     and sample composition must be well characterized.  The products
     of bioassays will be more useful if consistent with observational
     data (clinical and/or epidemiological).  For example, bioassay
     analysis on suspended particulate matter containing tobacco
     smoke obtained in homes and offices might help to elucidate
     the relative hazards of different environments.  A significant
     effort has been made (>$20 million) by the Department of Energy
     in recent years to provide a battery of chemical fractionation
     and bioassay techniques that can be used in complex mixtures.
     This useful published literature should be considered by the
     Agency in its health effects component.
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     D-   Reviews of Specific EPA Programs

          1.  Instrumentation


     The program described instruments developed primarily for measure-
ments of chemical exposure to selected air pollutants.  This work has
been successful and useful to field activities.  The prime focus has been
the development of passive and active sorbent collection devices that are
returned to the laboratory for analysis.  Plans were suggested to further
develop such approaches.  This does not seem a proper focus for continued
effort.  The types of measurement needs for field exposure assessment are
broad.  Requirements for real-time data, temporal and spatial resolution,
large dynamic range, and multidimensional measurements can never be
totally met by more or even better sorbent collection schemes.  Such
schemes have limitations and, therefore, must be complemented by others.

     The Panel recognizes the importance of instrumentation in meeting the
needs of exposure assessment; however, the current effort is not sufficiently
comprehensive at the existing level to meet these needs.  A recent
workshop at Harvard University sponsored by the EPA and the Gas Research
Institute defined the need for field instrumentation to perform exposure
measurement.  The latest technology in chemical monitoring (sensors
and detectors) should be used by EPA researchers to provide new concepts
and approaches for chemical pollutant measurement.  Such modern technologies
as integrated sensing systems (sensor arrays), fiber optic devices,
solid-state transducers, and electrochemical sensors can be applied to
field sensing problems and should be a part of the EPA's future instrumen-
tation research program.

     The development of instrumentation (and all field techniques) is related
to the prioritizing of compounds, situations, and parameters required in
exposure measurement studies.  Then, appropriate strategies (near—term and
long-range) should be proposed by instrument developers to satisfy these
most important needs using the best available technology.  The present
schemes for sorbent measurement have important field uses and should be
supported but should not be the main focus of future efforts.


          2.  Field Studies


     The EPA's measurement activities related to total human exposure to
environmental pollutants fall with the following areas:


     •  Statistical protocols and experimental design

     •  Microenvironmental field studies

     •  Total human exposure field studies
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     •  Dosage research  investigations

     The first three  topics  are  discussed  in (this  section;  dosage  research
will be discussed in  Section D.4 of  this report.

     a.   Statistical Protocols  and  Experimental Design  -  The  EPA  staff
          are to be commended for their  scientific contributions to
          development of the indirect  and  direct approaches to exposure
          assessment, and for their  early  recognition  of the critical
          role of survey sampling methodology  in development of valued
          exposure assessments.   This  work has raised  a  number of  out-
          standing critical  statistical  issues associated  with exposure
          assessment, such as:

          1)  optimal designs for direct  and indirect  exposure
              assessment studies;

          2)  statistical validity of  indirect exposure  assessment;

          3)  evaluation of  benefits (in reducing  uncertainty)
              versus  costs of various  levels of effort of  exposure
              measurement, with  regard to  both epidemiological studies
              and risk assessment.

          Methodologic research  to clarify these  issues  should be  encouraged,
          so  as  to determine the incremental value of  intensified  measurement
          programs in exposure assessment, and to  guide  the design of
          future studies.

     b.   Microenvironmental Field Studies - These studies characterize
          the pollutant concentrations to  which people are exposed when
          they  are in specific microenvironments.   Most  of the work
          conducted  so far is related  to carbon monoxide exposures.
          Clearly, additional studies  of the concentration distributions
          of  other pollutants in appropriate microenvironments are needed
          at  this stage.  Even within a single microenvironment (e.g.,  a
          parking garage), pollutant concentrations are  highly variable
          in  space and time, and great care must  be taken to obtain
          suitable measurements  so that these  concentration distributions
          can be accurately characterized.

          We  agree  that in future personal monitoring studies, the following
          should be  applied:

           1)  use of closed format questionnaires;

          2)  use of automated instrument output;  and

          3)   locating activities to specific census  tracts.

          These are  crucial lessons learned from the Denver and Washington
           carbon monoxide studies and will improve the validity of future
          studies.


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The objectives and expected benefits of the Exposure Methods
Test Site (EMTS) project are not clear to the Panel.  Although
there are advantages to having a single locale where micro-
environmental field studies can be conducted, it would be
dangerous to assume that the data obtained at such a locale
would be representative of exposures in other cities in other
parts of the country.  This is because of the many demographic,
geographic, and climatological differences between various
locations.  Hence, the Panel recommends that the degree to which
the data from an EMTS is expected to be generic and extrapolatable
be established before the project is implemented.

Total Human Exposure Field Studies - The Panel applauds the
EPA's efforts in conducting the TEAM study, and recommends that
comprehensive exposure studies of this type be continued and
expanded to include other pollutants and additional locations.
New developments in pollutant monitoring technology and biological
monitoring should be incorporated as they become available.

     Some of the findings of the studies conducted to date
suggest that greater attention should be given to incorporating
source-receptor considerations into the survey design.  In some
instances, it appears that much of the variability that shows
up in the exposure data could be explained by meteorological
factors, such as some receptors being downwind of the source(s),
while others are not.  A more careful experimental design that
includes consideration of these factors, including measurement
of appropriate meteorological parameters, will likely lead to
more meaningful data in future studies.

The following are some technical comments on TEAM:

1)   The intraperson temporal variation in VOC exposure is
     crucial in risk assessment and should be given a high
     priority in future studies.

2)   Given the substantial measurement error, the estimated
     exposure distributions can be substantially more hetero-
     geneous than the true exposure distributions.  For example,
     the variance of the estimated exposures is the sum of the
     variance of the true exposures and the variance of the
     measurement errors, assuming that: a) measurement errors
     are homoscedastic, and  b) there is no correlation between
     measurement error and true exposure.  Empirical Bayes
     methods are available for such adjustments.

3)   We share the concern about the high refusal rate in the
     sample enrollment.  We would like to see more rigorous
     efforts in the future to assess the impact of the refusal
     on the generalizability of the sample.  For example, a
     subsample of the accessible part of the refusals can be
     offered an incentive to participate, or be offered a less
     intensive protocol for their participation; the data from
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               the would-be refusals can then be compared with the "regular1
               participants to assess the possible magnitudes of selection
               bias.
         3.  Modeling
     As an alternative to direct personal monitoring of human exposure,
the indirect modeling approach offers certain attractive features and
has the potential to be cost effective.  The essence of the indirect
approach is to assess human exposure as it is related to human activities,
and to combine pollution measurements with activity data (which could be
collected separately) to estimate exposure.  Simulation models such as
SHAPE and NEM are variants of this approach in which either part or all
of the input data are simulated or imputed.

     Compared to the direct personal monitoring approach, the indirect
approach has the following advantages:

     a.   Existing pollution arid activity data can be reused in comparable
          future studies, thereby reducing the cost of future studies;

     b.   The human subjects need not be burdened with the inconvenience of
          carrying personal monitors during their activities;

     c.   In the absence of feasible personal monitors, it might still be
          possible to estimate exposure using the indirect approach as a
          stop-gap measure; and

     d.   In conjunction with source-transport models, the indirect
          approach can be used to impute the would-be exposures under
          alternative regulatory strategies.


     The presentation at the review meeting was focused on one aspect of
the indirect approach, namely, the use of microenvironmental monitoring
to collect pollution data.  The indirect approach can also be implemented
with pollution data from a personal monitoring study.  For example,
pollution data from an earlier personal monitoring study can be combined
with the activity data from a comparable sample in a new study.  Another
example is enhanced personal monitoring, in which extra activity data
are collected to make more efficient use of the pollution data.  We
recommend the collection of activity data in future studies whenever
feasible.

     The indirect approach remains to be validated empirically with
comparable personal monitoring data.  We endorse the plan to validate
the SHAPE model with actual field data and the mentioned effort by the
Agency's Office of Air Quality Planning and Standards (OAQPS) to validate
and modify the NEM model to accept empirical activity data as input.
Such validation would enhance the use of those models in future studies.
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     However, it is neither clear which microenvironments and chemicals are
of greatest importance nor how to define each microenvironment.  Further,
identification of the microenvironmental scenarios which will be most effective
at modeling exposure must be considered.  Subsequent to this prioritization
and analysis of microenvironments, cost effective research in this field
can be planned.

     Although the simulation modeling approach to estimating total human
exposures is not without difficulties and weaknesses, it is less costly
and potentially more generalizable than direct measurements.  The most
serious problem with the modeling approach is that, before any model can
be used with any confidence, its validity must be carefully and completely
evaluated.  This requires large quantities of experimental data from
specially designed field studies.  Failure to obtain a probability sample
for microenvironment monitoring is a shortcoming of the Washington micro-
environment study, and needs to be addressed in future studies.

     Logically, the direct (measurement) and indirect (modeling) approaches
should be considered complementary, in that the former provides essential
information for the development, validation, and refinement of the latter.
Hence, the Panel recommends that the planning for human exposure field
studies be carefully designed specifically to provide for the needs of
exposure models.


         4.  Dosage Research


     The Panel's review of the dosage research program was relatively
brief and occurred at the end of a long day.  Hence it was, of necessity,
somewhat superficial.  Nevertheless, we found that the choice of assays
to be included in this program review by the EPA staff was reasonable
and that productive work was being done.  The people involved appeared
to have a good grasp of the scientific issues and potential of their
methodology, and to be capable of undertaking additional productive work
in this important area.  The following are some specific comments:


     a.   The results of the analyses of volatile organic chemicals
          (VOC's) in exhaled air in the TEAM study provide an excellent
          example of the utility of such measurements in field studies.
          They showed that most of the VOC's were traceable to indoor
          rather than outdoor sources of air pollution, and identified
          many previously unsuspected causes of human pollutant exposures.

     b.   The results of the measurements of alveolar carbon monoxide
          in Denver and Washington were very useful in demonstrating
          that ambient carbon monoxide concentrations had very little
          effect on actual variation in individual overall exposures to
          carbon monoxide.
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c.   Current research on the use of short-term mutagenesis bioassays
     offer promise of developing reliable and efficient assays for
     source-specific pollutant mixtures from common indoor pollution
     sources such as cigarette smoke, wbodstoves and kerosene heaters,
     Research of this kind may prove to be useful to the EPA
     for many other applications involving exposure to organic
     vapors such as waste recovery and disposal sites.

d.   Evidence for human exposure to pollutants can often be made
     from analyses of biological materials such as exhaled air,
     urine, blood, hair, etc.  Such analyses are particularly
     valuable when there are multiple routes of exposure, and/or
     highly variable levels of exposure.  Biological samples can
     show evidence for cumulative exposures, and can indicate
     whether adverse effects are occurring or are likely to occur.
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APPENDICES

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                REVIEW PANEL ON TOTAL HUMAN EXPOSURE

                               CHARGE •
The purpose of the total human exposure research program is to
determine the frequency distributions of exposures of the pop-
ulations to selected chemicals.  The issues center around five
major topic areas:
     1)  Development of measurement methods,

     2)  Statistical protocols, data base development,
         and exposure models,

     3)  Microenvironmental field studies,

     4)  Total human exposure field studies,

     5)  Dosage research investigations.
     The Review Panel on Total Human Exposure shall advise the
Agency on how well the research program for Total Human Exposure
is progressing toward answering the needs of the Agency, including
both whether or not the right research is being conducted to address
the issues defined by the Research Committee process, and whether
the research is being conducted properly.  The Panel's findings and
recommendations will be presented both in a report and in a briefing
to be presented to the Deputy Administrator.
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               U.S. Environmental Protection Agency
                      Science Advisory Board
                Total Human Exposure Review Panel

                              Roster


Co-Chairmen

Dr. James Ware, Department of Biostatistics,  Harvard School of
     Public Health, 677 Huntington Avenue Boston, MA  02115

Dr. Morton Lippmann, Institute of Environmental Medicine, Lanza
     Laboratory, Long Meadow Road, New York University,  Tuxedo,
     NY 10987


Members
Dr. Lynn Anspaugh, Lawrence Livermore National Laboratory,  P.O.
     Box 5507; L-453, University of California, Livermore,  CA 94550

Dr. Naihua Duan, Economic Department, Rand Corporation,  1700
     Main Street, Santa Monica, CA  90406

Dr. Warren Johnson, Director, Atmospheric Science Center, Advanced
     Development Division, SRI International, 333 Ravenswood Avenue,
     Menlo Park, CA   94025

Dr. John Spengler, Harvard School of Public Health, Department
     of Environmental Science and Physiology, 665 Huntington Avenue,
     Boston, MA  02115

Dr. Joseph Stetter, Argonne National Laboratory, Building EES 362,
     9700 Cass Avenue, Argonne, IL   60439

Dr. Jerry Wesolowski, California Department of Health,
     2151 Berkeley Way, Berkeley, CA   94704
Executive Secretary
Mr. Robert Flaak, Science Advisory Board (A-101F), U.S. Environmental
     Protection Agency, 401 M Street, S.W., Washington, DC  20460
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