Climate Change Data Portal
DOI | 10.5194/acp-19-2765-2019 |
Towards a satellite formaldehyde - In situ hybrid estimate for organic aerosol abundance | |
Liao J.; Hanisco T.F.; Wolfe G.M.; Clair J.S.; Jimenez J.L.; Campuzano-Jost P.; Nault B.A.; Fried A.; Marais E.A.; Gonzalez Abad G.; Chance K.; Jethva H.T.; Ryerson T.B.; Warneke C.; Wisthaler A. | |
发表日期 | 2019 |
ISSN | 16807316 |
起始页码 | 2765 |
结束页码 | 2785 |
卷号 | 19期号:5 |
英文摘要 | Organic aerosol (OA) is one of the main components of the global particulate burden and intimately links natural and anthropogenic emissions with air quality and climate. It is challenging to accurately represent OA in global models. Direct quantification of global OA abundance is not possible with current remote sensing technology; however, it may be possible to exploit correlations of OA with remotely observable quantities to infer OA spatiotemporal distributions. In particular, formaldehyde (HCHO) and OA share common sources via both primary emissions and secondary production from oxidation of volatile organic compounds (VOCs). Here, we examine OA-HCHO correlations using data from summertime airborne campaigns investigating biogenic (NASA SEAC4RS and DC3), biomass burning (NASA SEAC4RS), and anthropogenic conditions (NOAA CalNex and NASA KORUS-AQ). In situ OA correlates well with HCHO (r = 0:59-0.97), and the slope and intercept of this relationship depend on the chemical regime. For biogenic and anthropogenic regions, the OA-HCHO slopes are higher in low NOx conditions, because HCHO yields are lower and aerosol yields are likely higher. The OA-HCHO slope of wildfires is over 9 times higher than that for biogenic and anthropogenic sources. The OA-HCHO slope is higher for highly polluted anthropogenic sources (e.g., KORUSAQ) than less polluted (e.g., CalNex) anthropogenic sources. Near-surface OAs over the continental US are estimated by combining the observed in situ relationships with HCHO column retrievals from NASA's Ozone Monitoring Instrument (OMI). HCHO vertical profiles used in OA estimates are from climatology a priori profiles in the OMI HCHO retrieval or output of specific period from a newer version of GEOS-Chem. Our OA estimates compare well with US EPA IMPROVE data obtained over summer months (e.g., slope = 0:60-0.62, r = 0:56 for August 2013), with correlation performance comparable to intensively validated GEOS-Chem (e.g., slope = 0:57, r = 0:56) with IMPROVE OA and superior to the satellite-derived total aerosol extinction (r = 0:41) with IMPROVE OA. This indicates that OA estimates are not very sensitive to these HCHO vertical profiles and that a priori profiles from OMI HCHO retrieval have a similar per-formance to that of the newer model version in estimating OA. Improving the detection limit of satellite HCHO and expanding in situ airborne HCHO and OA coverage in future missions will improve the quality and spatiotemporal coverage of our OA estimates, potentially enabling constraints on global OA distribution. © Author(s) 2019. |
语种 | 英语 |
scopus关键词 | aerosol; anthropogenic source; formaldehyde; oxidation; spatial distribution; temporal distribution; volatile organic compound; United States |
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/144600 |
作者单位 | Atmospheric Chemistry and Dynamic Laboratory, NASA Goddard Space Flight Center, Greenbelt, MD, United States; Universities Space Research Association, GESTAR, Columbia, MD, United States; University of Maryland Baltimore County, Joint Center for Earth Systems Technology, Baltimore, MD, United States; Department of Chemistry, University of Colorado, Boulder, CO, United States; Cooperative Institute for Research in the Environmental Sciences, University of Colorado, Boulder, CO, United States; Department of Atmospheric and Oceanic Sciences, University of Colorado Boulder, Boulder, CO, United States; School of Geography, Earth and Environmental Sciences, University of Birmingham, Birmingham, United Kingdom; Harvard-Smithsonian Center for Astrophysics, Cambridge, MA, United States; NOAA Earth System Research Laboratory, Chemical Sciences Division, Boulder, CO, United States; Department of Chemistry, University of Oslo, Oslo, Norway; Institute for Ion Physics and Applied Physics, University of Innsbruck, Innsb... |
推荐引用方式 GB/T 7714 | Liao J.,Hanisco T.F.,Wolfe G.M.,et al. Towards a satellite formaldehyde - In situ hybrid estimate for organic aerosol abundance[J],2019,19(5). |
APA | Liao J..,Hanisco T.F..,Wolfe G.M..,Clair J.S..,Jimenez J.L..,...&Wisthaler A..(2019).Towards a satellite formaldehyde - In situ hybrid estimate for organic aerosol abundance.Atmospheric Chemistry and Physics,19(5). |
MLA | Liao J.,et al."Towards a satellite formaldehyde - In situ hybrid estimate for organic aerosol abundance".Atmospheric Chemistry and Physics 19.5(2019). |
条目包含的文件 | 条目无相关文件。 |
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。