globalchange  > 气候变化与战略
DOI: 10.1073/pnas.2012218117
论文题名:
Quantification of organic aerosol and brown carbon evolution in fresh wildfire plumes
作者: Palm B.B.; Peng Q.; Fredrickson C.D.; Lee B.H.; Garofalo L.A.; Pothier M.A.; Kreidenweis S.M.; Farmer D.K.; Pokhrel R.P.; Shen Y.; Murphy S.M.; Permar W.; Hu L.; Campos T.L.; Hall S.R.; Ullmann K.; Zhang X.; Flocke F.; Fischer E.V.; Thornton J.A.
刊名: Proceedings of the National Academy of Sciences of the United States of America
ISSN: 0027-8424
出版年: 2020
卷: 117, 期:47
起始页码: 29469
结束页码: 29477
语种: 英语
英文关键词: Aircraft measurements ; Biomass burning ; Brown carbon ; Phenolic compounds ; Secondary organic aerosol
英文摘要: The evolution of organic aerosol (OA) and brown carbon (BrC) in wildfire plumes, including the relative contributions of primary versus secondary sources, has been uncertain in part because of limited knowledge of the precursor emissions and the chemical environment of smoke plumes. We made airborne measurements of a suite of reactive trace gases, particle composition, and optical properties in fresh western US wildfire smoke in July through August 2018. We use these observations to quantify primary versus secondary sources of biomass-burning OA (BBPOA versus BBSOA) and BrC in wildfire plumes. When a daytime wildfire plume dilutes by a factor of 5 to 10, we estimate that up to onethird of the primary OA has evaporated and subsequently reacted to form BBSOA with near unit yield. The reactions of measured BBSOA precursors contribute only 13 ± 3% of the total BBSOA source, with evaporated BBPOA comprising the rest. We find that oxidation of phenolic compounds contributes the majority of BBSOA from emitted vapors. The corresponding particulate nitrophenolic compounds are estimated to explain 29 ± 15% of average BrC light absorption at 405 nm (BrC Abs405) measured in the first few hours of plume evolution, despite accounting for just 4 ± 2% of average OA mass. These measurements provide quantitative constraints on the role of dilution-driven evaporation of OA and subsequent radical-driven oxidation on the fate of biomass-burning OA and BrC in daytime wildfire plumes and point to the need to understand how processing of nighttime emissions differs. © 2020 National Academy of Sciences. All rights reserved.
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被引频次[WOS]:99   [查看WOS记录]     [查看WOS中相关记录]
资源类型: 期刊论文
标识符: http://119.78.100.158/handle/2HF3EXSE/163365
Appears in Collections:气候变化与战略

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作者单位: Palm, B.B., Department of Atmospheric Sciences, University of Washington, Seattle, WA 98195, United States; Peng, Q., Department of Atmospheric Sciences, University of Washington, Seattle, WA 98195, United States; Fredrickson, C.D., Department of Atmospheric Sciences, University of Washington, Seattle, WA 98195, United States; Lee, B.H., Department of Atmospheric Sciences, University of Washington, Seattle, WA 98195, United States; Garofalo, L.A., Department of Chemistry, Colorado State University, Fort Collins, CO 80523, United States; Pothier, M.A., Department of Chemistry, Colorado State University, Fort Collins, CO 80523, United States; Kreidenweis, S.M., Department of Atmospheric Science, Colorado State University, Fort Collins, CO 80523, United States; Farmer, D.K., Department of Chemistry, Colorado State University, Fort Collins, CO 80523, United States; Pokhrel, R.P., Department of Atmospheric Science, University of Wyoming, Laramie, WY 82071, United States; Shen, Y., Department of Atmospheric Science, University of Wyoming, Laramie, WY 82071, United States; Murphy, S.M., Department of Atmospheric Science, University of Wyoming, Laramie, WY 82071, United States; Permar, W., Department of Chemistry and Biochemistry, University of Montana, Missoula, MT 59812, United States; Hu, L., Department of Chemistry and Biochemistry, University of Montana, Missoula, MT 59812, United States; Campos, T.L., Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder, CO 80301, United States; Hall, S.R., Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder, CO 80301, United States; Ullmann, K., Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder, CO 80301, United States; Zhang, X., Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder, CO 80301, United States; Flocke, F., Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder, CO 80301, United States; Fischer, E.V., Department of Atmospheric Science, Colorado State University, Fort Collins, CO 80523, United States; Thornton, J.A., Department of Atmospheric Sciences, University of Washington, Seattle, WA 98195, United States

Recommended Citation:
Palm B.B.,Peng Q.,Fredrickson C.D.,et al. Quantification of organic aerosol and brown carbon evolution in fresh wildfire plumes[J]. Proceedings of the National Academy of Sciences of the United States of America,2020-01-01,117(47)
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