Document bB40Z8oRwYDXqRgnqdRaNVDYo

Environmental Protection Agency Proposed Guidelines for Exposure Assessment; Request for Comments G03726 3 0 4 Federal Register / Vol. 49. No. 227 / Friday. November 23, 1984 / Notices ENVIRONMENTAL PROTECTION (1) Development of Mathematical Street S.W.. Washington. DC. between AGENCY Model Selection Criteria. the hours of 6:00 a.m. and 4:30 p.m. tFRL-2706-5] Proposed Guidelines for Exposure Assessment A large number of mathematical models are used to estimate a wide variety of parameters needed for estimating exposures. Guidance in the form of selection criteria are needed to Dated: November 9.1984. William D. Ruckelshaus, Administrator. t Contents f a g e n c y : Environmental Protection ensure that the most appropriate 1. Introduction Agency (EPA). mathematical model is used for each fl. General Guidelines and Principles j ACTION: Proposed Guidelines for Exposure Assessment and Request for Comments. su m m a r y : The U.S. Environmental Protection Agency is proposing Guidelines For Exposure Assessment (Guidelines). These Guidelines are proposed for use within the policy and procedural framework provided by the various statutes which EPA administers to guide Agency analysis of exposure data. We solicit public comment and will take public comment into account in revising these Guidelines. These Guidelines will be reviewed by the Science Advisory Board in meetings now tentatively scheduled for April 1985. These proposed Guidelines were developed as part of a broad guidelines development program under the auspices of the Office of Health and Environmental Assessment (OHEA), located in the Agency's Office of Research and Development. Consonant with the role of OHEA's Exposure Assessment Group (EAG) as the Agency's senior health committee for exposure assessment, the Guidelines were developed by an Agency-wide working group chaired by the Director of EAG. d a t e : Comments must be postmarked by January 22.1985. exposure parameter estimate. (2) Development of Guidance for Analysis of Metabolism Data. Guidance is needed to provide appropriate consideration of metabolism data in the calculation of whole body dose and in the extrapolation of whole organism dose from one species to another. (3) Definition of the Relationship Between Exposure Assessment and Epidemiology. Guidance is needed to ensure that pertinent parameters of exposure are measured in prospective epidemiologic studies. Methods providing the best estimates of exposure for retrospective and historical epidemiologic studies must be defined. (4) Development of Methods to Relate Exposures Measured by Personal Monitoring to Source Contributions. Guidance is needed to establish methods to relate exposures as measured by personal monitoring to controllable sources and to discriminate among possible sources and between background and anthropogenic sources. It is the Agency's intent to revise the Guidelines periodically to incorporate the results obtained irt the four research areas defined above as they become available. In addition to the publication of the Guidelines, the Agency also will provide A. Exposure and Dose B. Decision Path to Determine Scope of the Assessment C. Uncertainty ILLOrganization and Contents of an Exposure Assessment A. Overview B. Detailed Explanation of Outline 1. Executive Summary 2. Introduction 3. General Information 4. Sources 5. Exposure Pathways and Environmental Fate 6. Monitored or Estimated Concentration Levels 7. Exposed Populations 8. Integrated Exposure Analysis 9. References 10. Appendexes I. Introduction These Guidelines provide the Agency with a general approach and framework for carrying out human or nonhuman exposure assessments for specified pollutants. The Guidelines have been developed to assist future assessment activities and encourage improvement in those EPA programs that require, or could benefit from the use of exposure assessments. The Guidelines are procedural. They should be followed to the extent possible in instances where exposure assessment is a required element in the regulatory process or where exposure assessments are carried I a d d r e s s e s : Comments may be mailed technical support documents that out on a discretionary basis by EPA or delivered to: Dr. James W. Falco. contain detailed technical information management to support regulatory or Exposure Assessment Group (RD-689). needed to implement the Guidelines. programmatic decisions. Office of Health and Environmental Two of these technical reports entitled This document, by laying out a set of Assessment. U.S. Environmental Protection Agency. 401 M Street S.W., "Development of Statistical Distribution questions to be considered in carrying or Ranges of Standard Factors Used in out an exposure assessment, should help I Washington. DC 20460. Exposure Assessments" and avoid inadvertent mistakes of omission. FOR FURTHER INFORMATION CONTACT: "Methodology for Characterization of F.PA recognizes that gaps in data will be Dr. James W. Falco. Telephone: 202-475- Uncertainly in Exposure Assessments'* common, but the Guidelines will 8909. are currently available. Technical nevertheless serve to assist in SUPPLEMENTARY INFORMATION: reports for the four new guideline areas organizing the data that are available, Preliminary drafts of these Guidelines described above will be available at the including any new data developed as were sent out for review to 15 scientists time of publication of the corresponding part of the exposure assessment. It is and engineers in the field of exposure guideline section. These technical understood that exposure assessments assessment within government, support documents will be revised may be performed at many different universities in the United States and periodically to reflect improvements in levels of detail depending on the scope abroad, and the private sector. exposure assessment methods and new of the assessment. Comments received from these reviews, information or experience. These Guidelines should also promote generally favorable, were taken into Support documents used in the consistency among various exposure account in developing the Guidelines preparation of these Guidelines as well assessment activities that are carried proposed here. as comments received are available for out by the Agency. Consistency with In addition, as a result of the reviews, inspection and copying at the Public respect to common physical, chemical, four areas'requiring further research Information Reference Unit (202-382- and biological parameters, with respect were identified as follows: 5926). EPA Headquarters Library, 401 M to assumptions about typical exposure L Federal Register / Vol. 49, No. 227 / Friday, November 23. 1984 / Notices, 46305 situations, and with respect to the characterization of uncertainty of estimates, will enhance the comparability of results and enable the Agency to improve the state-of-the-art of exposure assessment over time through the sharing of common data and experiences. It is recognized that the main objective of an exposure assessment is to provide reliable data and/or estimates for a risk assessment. Since a risk assessment requires the coupling of exposure information and toxicity or effects information, the exposure assessment process should be coordinated with the toxicity/effects assessment. This document provides a common approach to format, which should simplify the process of reading and evaluating exposure assessments and thereby increase their utility in assessing risk. As the Agency performs more exposure assessments, the Guidelines will be revised to reflect the benefit of experience. II. General Guidelines and Principles A. Exposure and Dose Exposure has been defined by Committee E-47, Biological Effects and Environmental Fate, of the American Society for Testing and Materials, as the contact with a chemical or physical agent. The magnitude of the exposure is determined by measuring or estimating the amount of an agent available at the exchange boundaries, i.e.. lungs, gut, skin, during some specified time. Exposure assessment is the determination or estimation (qualitative or quantitative) of the magnitude, frequency, duration, and route of exposure. Exposure assessments may consider past, present, and future exposures with varying techniques for each phase, i.e., modeling of future exposures, measurements of existing exposure, and biological accumulation for past exposures. Exposure assessments 3Te generally combined with environmental and health effects data in performing risk assessments. In considering the exposure of a subject to a hazardous agent, there are several related processes. The contact between the subject of concern and the agent may lead to the intake of some of the agent. If absorption occurs, this constitutes an uptake (or an absorbed dose) which then may lead to health effects. When biological tissue or fluid measurements indicate the presence of a chemical, exposures can be estimated from these data. Presence of a chemical in such biological samples is the most direct indication that an exposure has occurred. The route of exposure generally impacts the overall exposure and should be considered in performing risk assessments. B. Decision Path to Determine Scope of the Assessment The first step in preparing an exposure assessment should be the circumscription of the problem at hand to minimize effort by use of a narrowing process. A decision logic path that describes this process is shown in Figure 1. As illustrated in Figure 1. the preliminary assessment and the in-depth assessment are two major phases in this logic path. The preliminary assessment phase should commence by considering what risk is under study and what law might regulate the exposure to the agent. Within this framework, a preliminary data base should be compiled from readily available scientific data and exposure information based on manufacturer, processor, and user practices. Next, the most likely areas of exposure (manufacuring, processing, consumer, distribution, disposal, ambient, water and food, etc.) should be identified. Since a complete data search has not been conducted, well-identified assumptions and order of magnitude estimates are used to further narrow the exposure areas of concern. K r.w * r m t nr------- I!/ <!(*! i. x t:;tc n r* rca 111*Hi*ufitfOSJ u siik t t Data from this preliminary exposure assessment can then be coupled with toxicity information to perform a preliminary risk analysis. As a result of this analysis, a decision will be made that either an in-depth exposure assessment is neqessary or that there is no need for further exposure information. The organization and contenta of an in-depth exposure assessment are given in the following section. In assembling the information base for either a preliminary assessment or a more detailed assessment, its adequacy should be ascertained by addressing the following considerations: .--Availability of information in every area needed for an adequate assessment; --Quantitative and qualitative nature of the data: --Reliability of information; --Limitations on the ability to assess exposure. C. Uncertainty Exposure assessments are based on monitoring data, simulation model estimates, and assumptions about parameters used in approximating aotual exposure conditions. Both data and assumptions contain varying degrees of uncertainty which influence the accuracy of exposure assessments. An evaluation of these uncertainties is important when the assessment is the basis for regulatory action. The uncertainty analyses performed will vary depending on the scope of the assessment, the quantity and quality of monitoring data collected, and the type and complexity of mathematical models used. A discussion of the types of analysis used for quantifying uncertainties in exposures is presented in the next section. III. Organization and Contents of an Exposure Assessment A. Overview A suggested outline for an exposure assessment document is given in Exhibit 1. The five major topics to be addressed within most exposure assessments are as follows: Source(s); Exposure Pathways: Monitored or Estimated Concentration Levels and Duration; Exposed Population(s); and Integrated Exposure Analysis. These five topics are appropriate for exposure assessments in general, whether the assessments are of global, national, regional, local, sitespecific. workplace-related, or other scope.The topics are appropriate for exposure assessments on new or existing chemicals and radionuclides. 46306 Federal-Register / Vol. 49, No. 227 / Friday, November 23, 194 / Notices They are also applicable to both single media and multimedia assessments. Since exposure assessments are performed at different levels of detail the extent to which any. assessment contains items listed in Exhibit 1 depends upon its scope. The outline is a guide to organize the data whenever (11 Population size and characteristics (2) Population location (3) Population habits 8. INTEGRATED EXPOSURE ANALYSIS a. Calculation of Exposure (T) Identification and characterization of the exposed populations and critical elements of the ecosystem (2) Pathways of exposure substance's release to the environment, consistent with the scope of the assessment, should be included, such as production, extraction, processing, imports, stockpiles, transportation, accidental/incidental production as a side reaction, and'natural sources. The - sources should.be located, and activities they are available. b. Human Dosimetry and Monitoring involving exposure to the substance B. Detailed Explanation o f Outline c. Development of Exposure Scenarios and should be identified. Profiles b. Uses. The substance should be 1. Executive Summary The "Executive Summary'Vshould be written so that it can stand on its own d. Evaluation of Uncertainty 9. REFERENCES 10. APPENDICES traced from its sources through various uses (with further follow-up on the products made to determine the as a miniature report Its main focus 3. General Information presence of the original material as an li should be on a succinct description of the procedures used, assumptions a. Identity. (1) Molecular Formula and' impurtiy), exports, stockpile increases, structure, synonyms, Chemical Abstract etc. 4 employed, and summary tables or charts Service number, Toxic Substance List of die results. A brief discussion of the number. c. Disposal. This subsection should contain an evaluation of disposal sites ;t uncertainties associated with the results (2) Description of technical grades, and destruction processes, such as should be included. contaminants, additives. incineration of industrial chemical Z. Introduction (Purpose and Scope) (3) Other identifying characteristics. wastes, incineration of the substance as b. Chemical and Physical Properties. ' part of an end-use item in municipal This section should state the intended This subsection should provide a waste, landfilling of wastes, biological purpose of the exposure assessment and summary description of the chemical destruction in a secondary wastewater identify the agent being investigated, the and physical properties of the agent treatment plant, or destruction in the types of sources and exposure routes Particular attention should be paid to process of using the end product. included, and the populations of the features that would affect its Hazardous contaminants of the concern. behavior in the environment Examples substance may be included, and Exhibit 1.--Suggested O utline for an Exposure A ssessm ent 1. EXECUTIVE SUMMARY 2. INTRODUCTION a. Purpose b. Scope of factors to be included are molecular weight density, boiling point, melting point, vapor pressure, solubility, pK*. partition coefficients, and half-lives. 4. Sources products containing the substance ao- contaminant may be followed freak: *- production through destruction/: v,---,jiiaposal. d. Summary o f Environmental Releases. Estimates should be made of 3. GENERALINFORMATION The points at which a hazardous - the quantities of the substances released (i a. Identity substance is believed to enter the to the various environmental media. (1) Molecular formula and structure. CAS environment should be described, along Sources of release to the environment * number, TSL number (Z) Description of technical grades. contaminants, additives (31 Other identifying characteristics with any known rates of entry. Points of include production, use, distribution/ entry may be indoors as well as transport, natural sources, disposal and outdoors, and environments include contamination of other products. b. Chemical and Physical Properties indoor settings such as offices as well as Environmental releases should be 4. SOURCES outdoor environments. A detailed presented at a reasonable level of detaiL a. Characterization of Production and exposure assessment should include a Extremely detailed exposure estimates Distribution (1) Production and processing (2) Distribution in commerce b. Uses c. Disposal d. Summary of Environmental Releases 5. EXPOSURE PATHWAYS AND study of sources, production, uses, des Eduction/disposal, and environmental release of a substance. The studies should include a description of human activities with respect to the substance and the environmental releases resulting would attempt to specify the following information for each significant emission source: Location, amount of the substances being released as a function of time to each environmental medium, physical characteristics of the emission ENVIRONMENTAL FATE from those activities. It should account source, and the physical and chemical a. Transport and Transformation for the controlled mass flow of the form of the substance being released. b. Identification of Principal Pathways of Exposure c. Predictmg^inviroiHMHtirf-Distribution 6. MONITORED.OR;ESTB4ATED CONCENTRATION LEVELS a. Summary of Monitoring DU b. Estimation of Environmental Concentrations c. Comparison of Concentration Estimates substance from creation to destruction and provide estimates of environmental releases at each step in this flow. Seasonal variations in environmental releases should also be examined. All sources of the substances should be accounted for with the sum of the uses, destruction, and the environmental Evaluation of the uncertainties associated with the emission estimates should be given. A detailed discussion of procedures for estimating uncertainty is presented in section 8.d. 5. Exposure Pathways and Environmental Fate with Monitoring Data 7. EXPOSED POPULATIONS a. Human Populations (Size, Location, and Habits) (1) Population size and characteristics (2) Population location (3) Population habits releases. The environmental releases can be described in terms of geographic and temporal distribution and the receiving environmental media, with the form identified at the various release points. The exposure pathways section should address how a hazardous agent moves from the source to the exposed population or subject. For a less detailed assessment, broad generalizations on environmental pathways and fate may b. Nonhuman Populations (where a. Characterization of Production and be made. In the absence of data, e.g., for appropriate) Distribution. All sources of the new substances, fate estimates may- Fcdwrf Register / Voi. 49, No. 227 / Friday, November 23, 1984- \ Notices 307 have to be predicted by analogy with data from other snbstances. Fate estimates may alea bermede by v&ing . models and/or and laboratory-derived pwa&rarratc coefficients. At a>y level of detail certain pathways may befadged insignficiant and not pursued farther. For more detailed assessments involving environmental fate, the sources analysis described previously should provide the amount and rate of emission to the environment, and possibly the locations and form of the emissions. The environmental pathways and fate analysis follows the substance from its point of initial environmental release, through,the environment to its ultimate fate. It may result in.an . estimation of the geographic and temporal distribution of concentrations of the substance in the various . contaminated environmental media. a. Transport and transformation. The substance, once released to the. environment, may be transported (e.g., convected downstream.in water or on * suspended sediment through the atmosphere, etc.) or physically transformed (e-g, volatilised, melted, absorbed/desorbed, etc.); may undergo chemical transformation such as photoyms. hydrolysis, oxidation, reduction; may undergo biotransfannation such a t biodegradation; or may accumulate in one or more media. Thus, the environmental behavior of a substance should be evaluated before exposures are assessed. Factors that should be addressed include: How does the agent behave in air, water, soil, and biological media? Does it bioaccumulate or biodegrade? Is it absorbed or taken up by plants? What are .the principal mechanisms for change or removal in each of the environmental media. Does the agent react with other compounds in the environment? Is there intermedia transfer? What are the mechanisms foe intermedia transfer? What are thjtBt.sitbe intermedia transfer orraatitkm mechanisms? :' How tong might the agent remain in each environmental medoaa? How does its concentration change with tune in each medium? What axe the products into which the agent might degrade or change in the environment? Are any of these degradation products ecologically or biologically harmful? W hat the environmental behavior of the harmful products? . Is a steady-state concentration distribution m the environment, or la specific segments of the environment, for chemical or radionuclide content achieved? If not. can the nonsteady- These data should be characterized as state distribution be described? to accuracy, precision, and What is the resultant distribution in representativeness. If actual the environment--for different media, environmental monitoring data are- different types or forms of the agent, for unavailable, concentrations can be different geographical areas, at different estimated by various means, including times or seasons? the use of fate models (see previous b. Identification o f Principal section) or. in the case of new Pathways of Exposure, The principal chemicals, by analogy with existing pathway analysis should evaluate the chemicals. sources, locations, and types of The analysis of monitoring data environmental releases, together with should be considered a complement to environmental behavioral factors, to environmental pathway and fate determine the significant routes of analysis for the following reasons: For human and environmental exposure to most pollutants, particularly organic and the substance. Thus, by listing the new chemicals, monitoring data are important characteristics of the limited; analysis of monitoring data does environmental release (entering media, not often yield relationships between emission fates, etc.) and the agent's environmental releases and behavior (intermedia transfer, environmental concentration persistence, etc.) after release to each of distribution fn media or geographic the entering media, it should be possible locations that have not been monitored;' to follow the movement of the agent analysis of monitoring data does not from its initial release to its subsequent provide information on how and where fate in the environment. At any point in biota influence the environmental the environment, human or distribution of a pollutant; and environmental exposure may occur. monitored concentrations may not be Pathways that result in major concentrations of the agent and high potential for human or environmental contact are the principal exposure pathways. c. Predicting Environmental Distribution. Models may be used to predict environmental distributions of chemicals. Many modeling estimates of environmental distribution of chemicals are based in part on monitoring data. In predicting environmental distributions of chemicals, available monitoring data should be considered. In this section an estimation is made, using appropriate models, of representative concentrations of the agent in different environmental media, and its time-dependence in specific geographical locations (e.g., river basins, streams, etc.). traceable to individual sources thatiEPA can regulate. Monitoring data are, however, a direct source of information for exposure analysis and. furthermore, they can be used to calibrate or extrapolate models or calculations to assess environmental distribution. b. Estimation o f Environmental Concentrations. Concentrations of agents should be estimated for aH environmental media that might contribute to significant exposures. Generally, the environmental concentrations are estimated from monitoring data, mathematical models, or a combination of the two. The concentrations must be estimated and presented in a format consistent with available dose-response information. In some cases an estimate of annual average concentration will be 8, Monitored or Estimated Concentration sufficient, while in other cases the Levels temporal distribution of concentrations a. Summary o f Monitoring Data. Monitoring data are used to identify releases (source terms) and, in the exposure pathways and fate assessments, to quantitatively estimate both release rates and environmental concentrations. Some examples of uses of monitoring data are: Sampling of stacks of discharge pipes for emissions to the environment; testing of products for chemical or radionuclide content; testing of products for chemical or radioactive releases; sampling of appropriate points within a may be required. Future environmental concentrations resulting from current or past releases may also be projected. In some cases, both the temporal and geographic distributions of the concentration may be assessed. Moreover, if the agent has natural sources, the contribution of these to environmental concentrations may be relevant. These "background** concentrations may be particularly important when the results of tests of toxic effects show a threshold or distinctly nonlinear dose-response. manufacturing plant to determine The uncertatrities associated with the releases from industrial processes or estimated concentrations should be practices; and sampling of solid waste - evaluated by an analysis of the- - 4630ft Federal Register / Vol. 49. No. 227 / Friday. November 23. 19S4 / Notices uncertainties of the model parameters and input variables. Whan the estimates of the environmental concentrations are based on aiathematiG&l_modfel&.the model results should be compared to available monitoring data, and any significant discrepancies should be discussed. Reliable, analyticallydetermined values should be given precedence over estimated values whenever significant discrepancies are found. 7. Exposed Populations Populations selected for study may be done a priori, but frequently the populations will be identified as a result of the sources and fate studies. From an analysis of the distribution of the agent, populations convected and subpopulations (i.e., collections of subjects) at potentially high explosure can be identified, which will then form the basis for the populations studied Subpopulations of high sensitivity, such as pregnant women, infants, chronically ill. etc., may be studied separately. In many cases, exposed populations can be described only generally. In some cases, however, more specific information may be available on matters ' such as the following: a. Human Populations. (1) Population size and characteristics (e.g,, trends, sex/age distribution} (2) Population location (3) Population habits--transportation habits, eating habits, recreational habits, workplace habits, product use habits, etc. b. Nonhuman Populations (where appropriate). (1) Population size and characteristics {e.g.. species, trends) [2) Population location (3) Population habits Census and other survey data may be used to identify and describe the population exposed to various contaminated environmental media. Depending on the characteristics-of available toxicological data, it may be appropriate to describe the exposed population by other characteristics such as SDecies. race-age-sex distribution, and health status. 8. Integrated Exposure Analysis The integrated exposure analysis combines the estimation of environmental concentrations (sources and fate information) with the description of the exposed population to yield exposure profiles. Data should be provided on the size of the exposed populations; duration, frequency, and intensity of exposure; and routes of exposure. Exposures should be related to sources. For more detailed assessments, the estimated environmental concentrations should be considered in conjunction with the geographic distribution of the human and environmental populations. The behavioral and biological characteristics of the exposed populations should be considered and the exposures of populations to various concentration profiles should be estimated.The results can be presented in tabular or graphic form, and an estimate of the uncertainty associated with them should be provided. a. Calculations of Exposure. The calculation of exposure involves two major aspects: (1) Identification of the Exposed Population and Critical Elements of the Ecosystem. The estimate of environmental concentrations also should give the geograhical areas and environmental media contaminated. The stated purpose of the assessment should have prescribed the human and environmental subjects for which exposures are to be calculated. If the subjects are not listed, the contaminated geographical areas and environmental media can be evaluated to determine subject populations. The degree of detail to be used in defining the exposed population distribution depends on the concentration gradient over geographic areas. (2) Identification of pathways of exposure. (a) Identification and description of the routes by which the substances travel from production site, through uses, through environmental releases/ sources, through transport and Fate processes, to the target population. (b) Quantitative estimates of the amounts of the chemical following each exposure pathway. Such estimates allow the various pathways to be put in the perspective of relative importance. From the geogrpahic and tempral distribution of environmental concentrations, the exposed population, the behavioral characteristics, and the critical elements of the ecosystem, exposure distributions can be estimated. The results of exposure calculation should be presented in a format that is consistent with the requirements of the dose-response functions which may later be used in a risk assessment. For example, when health risks caused by exposure over extended durations are considered, average daily exposure over the duration of exposure usually is calculated. When lifetime risks are ' considered, average daily exposure over a lifetime usually is calculated. In contrast, when health risks caused by exposures over short durations are considered, exposure rates are calculated over short time intervals to ensure that peak risks are defined. Many exposure assessments are based on the average exposure occurring over the exposure-period. The range of . possible exposures is usually divided into intervals, and the exposures within each interval are counted. The reuslts can be presented in a tabular form or as a histogram. The population residing in a specific geographic area may be exposed to a substance from several exposure routes. For each exposure route, exposure of individuals in these populations may be determined by summing the contribution of all sources to the exposure route. When exposures involve more than one exposure route, the relative amounts of a substance absorbed is usually route dependent. Consequently, total absorbed dose estimates must account for these differences. Because EPA regulates sources of releases, the contribution to exposures from each type of source being considered should be displayed. Exposure estimates should be presented for each significant exposure route (i.e.. those routes consistent with the regulatory purpose). -and the results should be tabulated in such a way that total externally applied and absorbed dose can be determined. b. Human Dosimetry and Monitoring. Biological monitoring of human body fluids and tissues for substances or their metabolites can be used to estimate current or past exposure to chemicals. When analytical methods are available, chemicals that have been absorbed into the body can be measured in body tissue and fluid. Such measurements can be used to estimate exposure. However, the substances to which humans are exposed are highly variable in the degree to which they leave in the body reliable indicators of exposure. Furthermore, although a compound may be relatively easy to detect in body tissue, for some compounds, attributing body burdens to specific environmental releases may be difficult because of limited ability to obtain environmental monitoring data. c. Development of Exposure Scenarios and Profiles. Depending on the scope of the exposure assessment, the total exposure may be fractionated into one or more "exposure scenarios" to facilitate quantification. As an example. Table 1 lists seven very broad scenarios; Occupational. Consumer, Transportation. Disposal. Food. Drinking Water, and Ambient. For each of the scenarios, the major topics necessary to quantify exposure include sources, pathways, monitoring: and population >9 Federal Register / Vol. 49, No. 227 / Friday, November 23, 1984 /. Notices/ 4831 characteristics. Investigation of only one scenario may be.necess&ry for the scope of some a sse ssm sz ^ Ib r example, a pesticide appficati^-expoijure assessment may^irifiifSier the occupational scenario which-would address the exposure to applicators and populations in the vicinity of the site. An exposure assessment around a hazardous waste site may focus on the disposal scenario. The exposure assessment also may consider other scenarios. The more extensive and comprehensive the scope, the more scenarios sire usually involved. Table 1. Exposure Assessment Needs for Various Exposure Scenarios E x ^ w t aceharto Scuca naadi Fata naadi Fopcttfon cfwractartric* naada Uorifetang naadi Occtpwtonal fcfw ric* jaoducttonVTM Sa*/pian terto n n -p * rV v a and propard** Worker*, tarnftn, popUMon- arwatd kvplarv/orvato ratocaaa, amt* malaria* balana. fftodvtak otae/ptant*. toraa njrotmdtog au^ptara tartan monaortng. Coneunar (*oct uaa o< OmmtcM or C o n aw to n rata*. attribution pal* PbyticaJ and cftanricat prapanto Conaumara------------------------------------------ Lava* n preduoa raaaaaa. inaewanant utfaL lam a n o tra n product*. rtefl raiwaat rata* modtia* TraM porwtoVsorsga/apito PaBama oI dtotrtbuecn v d tranapor- Fbysttf and cfwracal p n p id ia Stoag*. wnapormtot a v k a a , Aataaaaa, ambto* d w a. taflorc mod** to tpAe. anvvunrnanttJ fata modM, ganeral population art are*. Dtipo** (toctodo re n n fio n , tard- Uatotoa balana around ifapoul Fata aMn dapoa* prooaar. a n * Wortara * Ala of J u x M gannA nalaaaa* torto at wartoua port sp. method, afflomey. ratataae as an- tom m ra t tom of ralaaa; popdadon around ala. Wart pucaaj, a ritto l t o * woflnmnL modaiL Food________________ ___ Pood chan partaflfr* artWraa Food chart moda*, tat* dutag General pOpUatton, nortnuman pop- L M b to lend. to a d M i too* chat preparation or procaMng ot food. tlattov artotog. Drtoriog w ato- ,, _ .............. - Grotmdaato, aafaoa vatar, dtorttu- Laacfi ram tram papee. chtortoafton Sanaral poputotot.-- Lava* to drwong alar, grew* bon cynam. proewaaa. fat* in M r w w n ar. ariao a aato . la m e r ptoto. AffltMT*___________________ ___,, R aiaaj aa 10 amtonmant w , land. E n ^ o n m m l tata modala..-- . Cmm M po pirtw y nedfum n po^ M M A*. M . l l, c ; tu n s m o rin t It will usually be advantageous In performing an exposure assessment to identify exposure scenarios, quantify the exposure in each scenario, and then integrate the scenarios to estimate total exposure. In this "integrated exposure analysis," summation of independent exposures from different scenarios (keeping exposure routes separate] often will result in a breakout of exposure by subpopulations, since the individual scenarios usually treat exposure by subpopulation. Therefore, the integration of the scenarios, or integrated exposure analysis, will often result in an exposure profile. For each exposed subpopulation, exposure profiles should include the size of the group, the make-up of the group (age, sex, etc.], the source of the agent, the exposure pathways, the frequency and the intensity of exposure by each route (dermal, inhalation, etc.], duration of exposure, and the form of the agent when, exposure occurs. Assumptions and uncertainties associated with each scenario and profile.should be clearly discussed. . d. Evaluation o f Uncertainly. (1) Introduction. Often an-exposure assessment progress*-through several stages of refinement. The purpose of these Guidelines is to present methods appropriate for characterization of uncertainty for assessments at various stages of refinement, from assessments based upon limited initial data to those based upon extensive data. The appropriate method for characterizing uncertainty for an exposure assessment depends upon the underlying parameters being estimated, the type and extent of data available, and the estimation procedures utilized. The uncertainty of interest is always with regard to the population characteristic being estimated. For example, when the population distribution of exposures is being estimated, characterization of uncertainty addresses the possible differences between the estimated distribution of exposure and the true population distribution of exposure. An exposure assessment quantifies contact of a substance with affected population members (human or nonhuman subjects]. The measure of contact (e.g., environmental level of absorbed dose] depends upon what is needed to predict risk. An integrated exposure assessment quantifies this contact via all routes of exposure (inhalation, ingestion, and dermal) and all exposure pathways (e.g., occupational exposure, exposure from . consumption of manufactured goods, etc.). The exposed population generally is partitioned into subpopulations such that the likely exposure of all members of a subpopulation is attributable to the same sources. The exposure for each member of a subpopulation is then the sum of exposures over a fixed set of sources and pathways. The measured or estimated exposures for members of a subpopulation are ideally used to estimate the subpopulation distribution of exposure or characteristics thereof. However, a lack of sufficient information sometimes precludes estimation of the subpopulation distributions of exposure and only summary measures of this distribution. 9uch as the mean, minimum, maximum, etc., are estimated. In each case characterization of uncertainty for the . exposure assessment primarily addresses limitations of the data and the estimation procedures. The proportions of the population members in the individual subpopulations are usually estimated and can be used (by combining estimated distributions for the subpopulations) to estimate the distribution of exposure for the total population. Uncertainty concerning the sizes of the subpopulations should be addressed by discussing limitations of the data and estimation methods as well as by tabulating confidence interval estimates for the population sizes, whenever possible. (2) A ssessments-Based Upon Limited initial Data. The initial exposure assessment for a substance may be based upon limited data for exposure, and/or input variables for an exposure prediction model (he- an equation that expresses exposure as a function of one or more input variables). These data might be either extant data or data produced by an initial small-scale study. The initial limited data frequently are insufficient to permit estimation of the entire distribution of exposure. Instead, summary measures of this distribution, such as the mean, minimum, and maximum, are usually estimated. If the assessment is based upon measured exposures, the methoda-used. to characterize uncertainty depend mainly upon whether or not the data, result from a probability sample for which the probability of inclusion is known for each sample member. Characterization of uncertainty for an assessment based upon a probability sample of exposures is discussed .later in section 8. d, (5). If the measured exposures are not based upon a probability sample, acknowledgement V4 46310 Federal Register / Vol. 49, No. 227 / Friday, November 23. 1984 / Notices that no strictly valid statistical inferences can be made beyond the units actually in ins sample is one aspect of the characterization of uncertainty. If inference procedures are implemented. the issumpnons upon which these mferar.cc3 are based (e.g.. treatment cf the sample as if it was a simple random sample, or assumption of an underlying mt.de') should c-e explicitly slated and justified. The data collection methods and inherent limitations of the data should niso oe discussed. An initial exposure assessment also may be based upon limited data, such as estimated ranges, for input variables for an exposure prediction model. The exposure prediction model would be derived from a postulated exposure scenario that describes the pathways from sources to contact with population members. If the data were only sufficient to support estimates of the ranges of the input variables, the exposure assessment might be limited to a sensitivity analysis. The purpose of the sensitivity analysis would be to identify influential model input variables and develop bounds on the distribution of exposure. A sensitivity analysis would estimate the range of exposures that would result as individual model input variables were varied from their minimum to their maximum possible values with the other input variables held at fixed values, e.g.. their midranges. The overall minimum and maximum possible exposures usually would be estimated also. For an exposure assessment of this type, the uncertainty would be characterized by describing the limitations of the data used to estimate plausible ranges of model input variables and by discussing justification for the model. Justification of the model should include a description of the exposure scenario, choice of model input variables, and the functional form of the model. Sensitivity to the model formulation also can be investigated by replicating the sensitivity analysis for plausible alternative models. If the maximum possible exposure estimated by the sensitivity analysis presented no significant health risk, there might be no need to refine the assessment. If both the minimum and maximum exposures presented a potentially significant health risk, it would be known that the exposure scenario represented a significant health problem without refining the assessment. When the minimum exposure estimate does not present a potentially significant health risk and maximum dose, then greater importance is placed on choosing a summary para ".e'er of the exposure distribution [e.g.. the mean or percentile; as the b-tsis for a regulatory decision. Refining the exposure csse^sm.ent to *''*lTate the distribution of exposure p=rr.us , elecfon. of any si.mr..-.ry (minimum, mavmu.r.. riH:;n. or perccr.ttie. rc.i as th* *.!*< for regulatory dec.sion. The sons:*..', .tv eiudv 'is cor. t: enhanced by cumpu-:-; i `he predicted exposures that re:-jit _!! possible input variable combinations, if auch input variable has c **.!;. ; fir., if; set of possible values, the -f all possible combinations of the rput v.;r:anles can be formed, and the predicted exposure can be computed fur each combination. These exposure predictions can be used to form a distribution of exposures by counting the number of occurrences of each exposure or interval of exposures. This is equivalent to estimating the distribution of exposures that results from treating all input variable combinations as equally likely. This procedure can aiso be applied by discretizing continuous input variables and representing them by equallyspaced points. In ;he limit, as the equal spaces become small and the number of points becomes large, the distribution of exposure that results from counting occurrences of exposure levels is equivalent to estimating the distribution of exposures that results from stalistically-independent. continuous input variables with uniform distributions on the estimated ranges. This estimated distribution of exposure values can be produced by the methods of mathematical statistics or Monte Carlo simulation. The Monte Carlo method consists of randomly generating input variate values and using these to compute corresponding exposure levels, generating an exposure distribution via many iterations. Interpretation of statistics based upon this exposure distribution would be in terms of the equally likely input variable combinations. For example, the 95th percentile of this distribution would be the exposure level exceeded by only 5^ of the exposures resulting from treating all combinations of input variable values as equally likely. Although this distribution of exposures cannot be interpreted a3 an estimate of the population distribution (unless the input variables actually are statistically independent and uniformly distributed), it provides additional information for making regulatory decisions. Characterization of uncertainty would- include a discussion oflimitations of the data and justification for the model as discussed above. Sensitivity to muds! formulation cou'd also be investigated cy estimating the distribution if exposure that resuils from using ths* same uniform input variable distributions with plausible a models and comparing the es:. ,ti>ed percent ties. ,(3 i A?sessm$rrs Sssed L'pjr, Sttb;erav? Estimates of input l ev Distributions. If a model has been formulated that expresses exposure as i function of one or mere input variables, the methods of mathematical stntNucs or Monte Carlo simulation can be used to estimate the population distribution of exposure from an estima'e of *he iomt distribution of the model input variables. Ideally model input variables should be represented by empirically validated probability distributions, in some cases, it may be possible to formulate an estimate of the m. v distribution of model input from discussions with subject-matter experts (e.g.. via histograms for statistically-independent input variables). The estimated population distribution of exposure will be equivalent to the distribution discussed in section 8. d. (2) for equally likely combinations of input variable values only when the input variable distributions supported are independent uniform distributions. When qualitative knowledge of input variable distributions is ued to estimate the population distribution of exposure, uncertainty is characterized by discussing justification For the presumed model and input variable distributions. Alternative models and/or alternative input variable distributions also should be discussed. Sensitivity to these alternatives can be investigated by estimating the distributions of exposure that resuit from plausible alternatives and comparing the percentiles of the estimated exposure distributions. All available data, even if data are limited, should be used to validate the presumed input variable distributions and the predicted distribution of exposure. (4) Assessments Based Upon Data for Model Input Variables. The exposure assessment based upon an estimate of the joint probability distribution for model input variables can be refined by collecting sample survey data for model input variables for a sample of population members. The population distribution of exposure can then be estimated by computing the expected exposure for each sample member based upon the model. These expected exposures can be used to directly compute confidence interval estimates for percentiles of the exposure Federal Register / Vol. 49. No. 227 / Friday. November 23. 1984 / Notices 46311 distribution. Alternatively, the sample survey data can be used to compute joint confidence interval estimates for percentiles of the input variable distribution, which can then he used to generate confidence interval estimates for percentiles of the exposure distribution. In either case, the interval estimates for percentiles of the exposure distribution are a useful quantitative characterization of uncertainty. Characterization of uncertainty for the exposure assessment would contain a thorough discussion of limitations of the data and justification for the model used to compute expected exposures. The design of the sample survey used to produce the data base should also be discussed. If a probability sample were not used, the lack of a probability sample would be an additional source of uncertainty. Any assumptions used in computing the confidence interval estimates, such as independence of model input variables, should be explicitly stated and justified. Sensitivity to model formulation can be investigated by estimating the distribution of exposure for plausible alternative models and comparing the estimated percentiles, if sample survey data have been collected for the input variables of the alternative models. discussed. If the sample was not a Appropriate available data for exposure probability sample, this would again be should be used to validate the predicted in additional source of uncertainty. distribution of exposure. If specific 1*6j Summary. A summary of the probability distributions hpve been primary methods recommended for ' \ presumed for any model input variables, characterizing uncertainty in exposure the data for these variables should be assessments is presented in Table 2. used to test for goodness of fit for these Virtually all exposure assessments, distributions. (5) Assessments Based Cpon Data for Exposure. A major reduction in the uncertainty associated with an exposure assessment can be achieved by directly measuring the exposure for a sufficiently large sample of members of the affected population. This reduction in uncertainty is achieved by eliminating except those based upon measured exposure levels for a probability sample of pop-i'aticn members, rely upon a model.to predict exposure. The model may be any mathematical function, simple or complex, that expresses <m individual's exposure as a function of one or more input variables. Whenever the use of a model to pre-lie* exposure. a model that has not been validated is The measured exposure levels can be used as the basis for an exposure used to directly estimate the population assessment, the uncertainty associated distribution of exposure and confidence with the exposure assessment may be interval estimates for percentiles of the substantial. The primary exposure distribution. Direct confidence characterization of uncertainty is at interval estimates also can be computed least partly qualitative in this case, i.e . for other characteristics of the exposure it includes a description of the distribution, such as the mean exposure. assumptions inherent in the model and These confidence interval estimates their justification. Plausible alternative are then the primary characterization of models should be discussed. Sensitivity uncertainty for the exposure of the exposure assessment to model assessment. Limitations of the data and formulation can be investigated by design of the sample survey used to replicating the assessment for plausibie collect the data also should be alternative models. Table 2.--Summary of Primary Methods for Characterizing Uncertainty pop Exposure Assessments Type and extent of date I Population characteristic being estim ated t Primary memoos >or characterizing uncertainty Q ualitative m ethod* ! O uannaw e mem ot Measured exposures fo r a large samote of ! D istribution of exposure........... ............................. 1. Lim itations of tie survey O trtxjn and m eav j 1 Confidence ntervaJ ornate ter percent- population members. uiem ent teeftmoues. i -*es of the exocsure ostnbueon. 1 ! 2. Goocness o i h i tor evoosixe m odets, <t m y I nave been postulated. Measured exposures *or a sm all sample o l j Summary param eter^) of the exposure jfcatn- ; i Lim itations o f me uxvev oes>gn and mesa- ! i Connoence Jitervai asomatee lor mo sum. poputaoon members. ! ouDon. e g., mean or a percentile, I m om ent technique*. 1 mary param eterts). ! 2 G oocresa ol W for expoeure m odels, if any ` nave seen postulated. Measured model input vanaeies for a targe SD istribution of exposure......................................... I 1, Lim itations of me Survey design and -wees- ; 1 C cnhcerce .ntervel estim ates lo r percent. sample of population members. | uiem ent ecnnxxres. ; 'les of me exposure drambution. 12; V alidity i t ;ne exposure ooo ef . .. 2. ooocness of 'ri 'or .nput vsnaoie tftstnbu- I t non *upcnons. I any nave been postulated, j 3. Estim ated sistrbu&on of exposure cased I je o n a.terns"ve models, Estim ated astnbutions of m odel inou vane- Q istrbutw n of exposure............. t rarw ity of me exposure mooe* t Conhcence ntervai estim ate* tor pexcent- Dies. * i >es ol me exposure distribution. i 2. L.mrtanons at me data v other oasis 'or 2. Goocness of ot tor nput variable *stn tx> tr.e input variable asm busons. nens, .1 -rgu i vename data are avaaene. j 3. Estimated distribution ol exposure based upon alternative modera. Lim ited data for mode* mput variables......... . . Minimum, maximum, and range of me expo- 1. Lim itations oi me data-.- ... if Y' Put vsnaoie data are very (united. e,g,, j sure drain Dunon. 2. validity ol me exposure m o o e f........ , some extant data collected tor other w *. , poses, cuanotatrva charactenzaDon of un- i cenainty may not ,5e possible When an exposure assessment >s based upon directly measured exposure levels for a probability sample of population members, uncertainly can be greatly reduced and described quantitatively. In this case, the primarysources of uncertainty are measurement errors and sampling errors. The effects of these sources of error are measured quantitatively by confidence interval estimates of percentiles of the exposure distribution. Moreover, the sampling errors can be limited by taking a large sample. Whenever the latter is not feasible, it is sometimes possible to obtain t least some data for exposure and model input variables. These data should be used to assess goodness of fit of the model and/ or presumed distributions of input variables. This substantially reduces the amount of quantitative uncertainty for estimation of the distribution of exposure and is strongly recommended. It is recognized, however, that it may not be feasible to collect such data. 9. References The references should contain a listing of ail reports, documents, articles, memoranda, contacts, etc. that have been cited in the report. 10. Appendices ** 46312 Federal Register } Vot. 49. No. 227 / Friday. November 23, 1984 / Notices The appendices may contain such , items as memoranda and letters that a re * _ - not readily accessible, other tables of monitoring data.,detailed lists of emission sources, detailed tables of exposures, process flow diagrams, mathematical model formulations, or any other item that may be needed to describe or document the exposure assessment. I'm Doc. M-MTZJ Filed ll-ft-M : *49 am} BILUMQ COO I 5M -W -M V