Spatial variability of carbonaceous aerosols and associated source tracers in two cites in the Midwestern United States

被引:28
|
作者
Snyder, David C. [1 ]
Rutter, Andrew P. [1 ]
Worley, Chris [1 ]
Olson, Mike [1 ]
Plourde, Anthony [2 ]
Bader, Rebecca C. [1 ]
Dallmann, Timothy [1 ]
Schauer, James J. [1 ,2 ]
机构
[1] Univ Wisconsin, Environm Chem & Technol Program, Madison, WI 53706 USA
[2] Wisconsin State Lab Hyg, Madison, WI 53718 USA
关键词
Urban aerosols; Chemical mass balance; Carbonaceous aerosols; Aerosol source apportionment; POLYCYCLIC AROMATIC-HYDROCARBONS; FINE PARTICULATE MATTER; HUMAN CELL MUTAGENICITY; AIR-POLLUTION; ELEMENTAL CARBON; SOURCE APPORTIONMENT; ORGANIC-CARBON; RESPIRATORY HEALTH; DIESEL EXHAUST; MEXICO-CITY;
D O I
10.1016/j.atmosenv.2010.02.004
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Semi-continuous and 24-h averaged measurements of fine carbonaceous aerosols were made concurrently at three sites within each of two U.S. Midwestern Cities; Detroit, Michigan and Cleveland, Ohio; during two, one-month intensive campaigns conducted in July of 2007 and January & February of 2008. A comparison of 24-h measurements revealed substantial intra-urban variability in carbonaceous aerosols consistent with the influence of local sources, and excesses in both PM2.5 organic carbon (OC) and elemental carbon (EC) were identified at individual sites within each city. High time-resolved black carbon (BC) measurements indicated that elemental carbon concentrations were higher at sites adjacent to freeways and busy surface streets, and temporal patterns suggested that excess EC at sites adjacent to freeways was dominated by mobile source emissions while excesses in EC away from traffic corridors was dominated by point/area source emissions. The site-to-site variability in OC concentrations was approximately 7% within the neighborhood scale (0.5-4 km) and between 4 and 27% at the urban scale (4-100 km). In contrast, measurements of organic source tracers, in conjunction with a Chemical Mass Balance (CMB) source-apportionment model, indicated that the spatial variation in the contribution of both mobile and stationary sources to PM2.5 OC often exceeded the variation in DC mass concentration by a factor of 3 or more. Markers for mobile sources, biomass smoke, natural gas, and coal combustion differed by as much as 60% within the neighborhood scale and by greater than 200% within the urban scale. The observations made during this study suggest that the urban excess of carbonaceous aerosols is much more complex than has been previously reported and that a more rigorous, source-oriented approach should be taken in order to assess the risk associated with exposure to carbonaceous aerosols within the industrialized environments of the Midwestern United States. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1597 / 1608
页数:12
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