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DOI10.5194/acp-19-13209-2019
Biogenic secondary organic aerosol sensitivity to organic aerosol simulation schemes in climate projections
Cholakian A.; Beekmann M.; Coll I.; Ciarelli G.; Colette A.
发表日期2019
ISSN16807316
起始页码13209
结束页码13226
卷号19期号:20
英文摘要Organic aerosol (OA) can have important impacts on air quality and human health because of its large contribution to atmospheric fine aerosol and its chemical composition, including many toxic compounds. Simulation of this type of aerosol is difficult, since there are many unknowns in its nature and mechanism and processes involved in its formation. These uncertainties become even more important in the context of a changing climate because different mechanisms, and their representation in atmospheric models, imply different sensitivities to changes in climate variables. In this work, the effects caused by using different schemes to simulate OA are explored. Three schemes are used in this work: (1) a molecular scheme; (2) a standard volatility basis set (VBS) scheme with anthropogenic aging; and (3) a modified VBS scheme containing functionalization, fragmentation and formation of nonvolatile secondary organic aerosol (SOA) for all semi-volatile organic compounds (SVOCs). Five years of historic and five years of future simulations were performed using the RCP8.5 climatic scenario. The years were chosen in a way to maximize the differences between future and historic simulations. The study focuses on biogenic SOA (BSOA), since the contribution of this fraction of BSOA among OA is major in both historic and future scenarios (40 % to 78 % for different schemes in historic simulations). Simulated OA and BSOA concentrations with different schemes are different, with the molecular scheme showing the highest concentrations among the three schemes. The comparisons show that for the European area, the modified VBS scheme shows the highest relative change between future and historic simulations, while the molecular scheme shows the lowest (a factor of 2 lower). These changes are largest over the summer period for BSOA because the higher temperatures increase terpene and isoprene emissions, the major precursors of BSOA. This increase is partially offset by a temperature-induced shift of SVOCs to the gas phase. This shift is indeed scheme dependent, and it is shown that it is the least pronounced for the modified VBS scheme including a full suite of aerosol aging processes, comprising also formation of nonvolatile aerosol. For the Mediterranean Sea, without BVOC emissions, the OA changes are less pronounced and, at least on an annual average, more similar between different schemes. Our results warrant further developments in organic aerosol schemes used for air quality modeling to reduce their uncertainty, including sensitivity to climate variables (temperature). © 2019 Author(s).
语种英语
scopus关键词aerosol; air quality; atmospheric modeling; computer simulation; concentration (composition); seasonal variation; sensitivity analysis; uncertainty analysis; volatile organic compound; Mediterranean Sea
来源期刊Atmospheric Chemistry and Physics
文献类型期刊论文
条目标识符http://gcip.llas.ac.cn/handle/2XKMVOVA/144073
作者单位LISA, UMR CNRS 7583, Université Paris Est Créteil et Université de Paris, Institut Pierre Simon Laplace (IPSL), Créteil, France; Institut National de l'Environnement Industriel et des Risques, Parc Technologique ALATA, Verneuil-en-Halatte, France; EPOC, UMR 5805, Université de Bordeaux, Pessac, France; Department of Chemical Engineering, Carnegie Mellon University, Pittsburgh, United States
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Cholakian A.,Beekmann M.,Coll I.,et al. Biogenic secondary organic aerosol sensitivity to organic aerosol simulation schemes in climate projections[J],2019,19(20).
APA Cholakian A.,Beekmann M.,Coll I.,Ciarelli G.,&Colette A..(2019).Biogenic secondary organic aerosol sensitivity to organic aerosol simulation schemes in climate projections.Atmospheric Chemistry and Physics,19(20).
MLA Cholakian A.,et al."Biogenic secondary organic aerosol sensitivity to organic aerosol simulation schemes in climate projections".Atmospheric Chemistry and Physics 19.20(2019).
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