Wexler, A.S., Lurmann, F.W. and Seinfeld, J.H. Modeling urban and regional aerosols: I. Modeldevelopment. Atmos. Environ., 28, 531-546, 1994.Chapter 5 - General:1. The chapter on exposures is a vast improvement over <strong>the</strong> previous version.2. The chapter provides a reasonable summary <strong>of</strong> all recent studies on exposure, andinterpretative analyses <strong>of</strong> previous work.3. Un<strong>for</strong>tunately in <strong>the</strong> attempt to be current, <strong>the</strong> authors have <strong>for</strong>gotten to put some majorconcepts and results into a historical context. Some <strong>of</strong> <strong>the</strong> recent studies look as if <strong>the</strong>y arepresenting <strong>the</strong> first set <strong>of</strong> results on a particular issue. They clearly build upon previousresearch. This should be acknowledged by referring to previous criteria document (AQCD,1996) <strong>for</strong> fur<strong>the</strong>r in<strong>for</strong>mation on specific concepts.4. There is still an over-emphasis on correlations. I have stated be<strong>for</strong>e, an “association(correlation) makes <strong>the</strong> poison” is not a valid concept. Every particle that deposits in <strong>the</strong> lungbecomes part <strong>of</strong> a dose delivered to <strong>the</strong> individual. Although <strong>the</strong> variability is very relevant toresults obtained in many epidemiological studies that support PM health effects, no one has yetshown that a constant or “quasi-constant” baseline level <strong>of</strong> PM from indoor or personal sourcesis irrelevant in causing health effects. This point is mentioned in <strong>the</strong> integration chapter (9), butnot in chapter 5. The variable portion may provide <strong>the</strong> final stress to individuals who has hadsustained contact and deposition <strong>of</strong> particles from all sources. So, both E ag and E ig may havepartial influence on <strong>the</strong> ultimate dose affecting an individual at risk <strong>for</strong> one or more diseaseendpoints, especially potential acute effects.5. The chapter needs ano<strong>the</strong>r E descriptor, E ov-rxn-iv or E (ioRn) . This is PM exposure derived fromoutdoor vapor (ov) reacting (rxn) with indoor vapors (iv). This is a source that could also varywith outdoor PM when <strong>the</strong> (ov) is ozone.6. The range and distribution <strong>of</strong> many variables that affect PM penetration and deposition arenicely presented in <strong>the</strong> discussion. However, <strong>the</strong>se are never integrated and placed into a finalcontext <strong>for</strong> <strong>the</strong> uncertainties about <strong>the</strong> conclusions. The entire discussion is still attempting tosteer us to a mean value <strong>for</strong> exposure used in epidemiological studies, a point that is wellestablished. Un<strong>for</strong>tunately, <strong>the</strong> current approach ignores <strong>the</strong> distributional aspects <strong>of</strong> exposure tooutdoor and o<strong>the</strong>r sources. It precludes fur<strong>the</strong>r ef<strong>for</strong>ts in <strong>the</strong> staff paper to mention <strong>the</strong>uncertainties about <strong>the</strong> dose <strong>of</strong> specific agents or <strong>the</strong> entire mixture <strong>of</strong> PM from indoor andoutdoor air, which could be relevant to acute or chronic outcomes. It precludes any discussion in<strong>the</strong> staff paper on <strong>the</strong> variety <strong>of</strong> exposures and sources, which may cause health effects. I do notbelieve <strong>the</strong> major ion contributing to <strong>the</strong> mean PM (e.g., SO 4-2) is necessarily <strong>the</strong> chemical <strong>of</strong>concern. It may be an indicator, but we still need to define what it is an indicator <strong>of</strong> -- ambientPM 2.5 mass or toxic sub-fractions.7. Last conclusion is a working hypo<strong>the</strong>sis, but it is not <strong>the</strong> sole reason <strong>for</strong> understandingexposure. We need to eventually determine which dose or doses contribute to acute or chroniceffects. The statement needs to be modified accordingly.Detailed Comments:P. 5.6, Table 5.1 Very good summary.P. 5.7, Line 6 We have no definitive “outer limit” it is still a guess, and/or convenientlocation on <strong>the</strong> person. It is usually found somewhere within <strong>the</strong> personalenvelop <strong>for</strong> inhalation.P. 5.8, Line 21 Integral referenced to, NRC 1991. It was published previously by Lioy,A - 37
1990. Reference Lioy, P.J. “The Analysis <strong>of</strong> Total Human Exposure <strong>for</strong>Exposure Assessment: Multi-Discipline Science <strong>for</strong> Examining HumanContact with Contaminants“ Environmental Science & Technology, 24,938-945, 1990.P. 5.11 Good summary <strong>of</strong> published activity pattern data.P. 5.13 to 5.14, 5.3.2.2.2 Very simple explanation <strong>of</strong> mass balance model. Authors need toremind readers that all variables have ranges, and in some casesmay change in value by a factor <strong>of</strong> 5 to 10. There<strong>for</strong>e, sensitivityand uncertainty analysis are necessary when attempting to explainresults.5.3.2.3 The equation is a linear simplification <strong>of</strong> exposure and ignores possiblesynergisms. The authors need to provide qualifiers here!5.3.2.3.1 Need to state that equilibrium is a simplification <strong>of</strong> indoor systems that areoccupied by residents. Thus, equilibrium may only represent a “virtual”set <strong>of</strong> individuals or populations at potential risk. The alpha in Equation5-9 can, and will, vary based upon lifestyle, meteorology, etc.Also, need qualifiers because <strong>of</strong> personal activities, housingcharacteristics, and particle size and composition.P. 5.19 Very good introduction, and Table 5.4 is well done. There are o<strong>the</strong>rs, butmost are still work in progress (e.g., RIOPA study by Weisel et al; COPDby Koutrakis, et al.). Table 5.5 good summary table.P. 5.30 Mage – Qualify to “average person” in PTEAM.P. 5.31 to 5.35 The net result is that <strong>the</strong>re are many different types <strong>of</strong> correlations and youcan get many different results. Conclusion, we still need and more workon which variable(s) is (are) needed to represent personal ambientexposure. This is essential <strong>for</strong> assessing which compounds and whichexposures cause <strong>the</strong> observed effects.P. 5.37, Lines 9-10 A low correlation doesn’t mean much, r 2 < 0.05!P. 5.39, Lines 29-30 Is “tracked” <strong>the</strong> right term? This only explains 25% <strong>of</strong> variability.P. 5.41 Subjects in Baltimore were very sedentary!! Could <strong>the</strong>se individuals bedescribed as stationary personal monitors?P. 5.41 Sulfate is an indicator <strong>of</strong> ammonium sulfate, and not even <strong>the</strong> dominantacid species (sulfuric acid, ammonia bisulfate). In areas where <strong>the</strong>re arelarge organic, or nitrate loadings, <strong>the</strong> SO 4-2ion may not be an indicator <strong>of</strong>those portions <strong>of</strong> <strong>the</strong> mass. I think SO 4-2is an indicator <strong>of</strong> <strong>the</strong> variability<strong>of</strong> aged secondary aerosol in <strong>the</strong> fine fraction.P. 5.41, Lines 26-27 Confusing. SO 4-2is a strong indicator <strong>of</strong> neutralized sulfur particulateexposure, where <strong>the</strong>re are no indoor sources. In contrast, PM 2.5 has manysources besides SO 4-2.P. 5.43, Lines 6-8 Is this <strong>the</strong> appropriate way to interpret <strong>the</strong>se data?A - 38
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