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DOI | 10.5194/acp-21-8003-2021 |
Analysis of secondary organic aerosol simulation bias in the Community Earth System Model (CESM2.1) | |
Liu Y.; Dong X.; Wang M.; Emmons L.K.; Liu Y.; Liang Y.; Li X.; Shrivastava M. | |
发表日期 | 2021 |
ISSN | 1680-7316 |
起始页码 | 8003 |
结束页码 | 8021 |
卷号 | 21期号:10 |
英文摘要 | Organic aerosol (OA) has been considered as one of the most important uncertainties in climate modeling due to the complexity in presenting its chemical production and depletion mechanisms. To better understand the capability of climate models and probe into the associated uncertainties in simulating OA, we evaluate the Community Earth System Model version 2.1 (CESM2.1) configured with the Community Atmosphere Model version 6 (CAM6) with comprehensive tropospheric and stratospheric chemistry representation (CAM6-Chem) through a long-term simulation (1988-2019) with observations collected from multiple datasets in the United States. We find that CESM generally reproduces the interannual variation and seasonal cycle of OA mass concentration at surface layer with a correlation of 0.40 compared to ground observations and systematically overestimates (69 %) in summer and underestimates (-19 %) in winter. Through a series of sensitivity simulations, we reveal that modeling bias is primarily related to the dominant fraction of monoterpeneformed secondary organic aerosol (SOA), and a strong positive correlation of 0.67 is found between monoterpene emission and modeling bias in the eastern US during summer. In terms of vertical profile, the model prominently underestimates OA and monoterpene concentrations by 37 %-99% and 82 %-99 %, respectively, in the upper air (>500 m) as validated against aircraft observations. Our study suggests that the current volatility basis set (VBS) scheme applied in CESM might be parameterized with monoterpene SOA yields that are too high, which subsequently results in strong SOA production near the emission source area. We also find that the model has difficulty in reproducing the decreasing trend of surface OA in the southeastern US probably because of employing pure gas VBS to represent isoprene SOA which is in reality mainly formed through multiphase chemistry; thus, the influence of aerosol acidity and sulfate particle change on isoprene SOA formation has not been fully considered in the model. This study reveals the urgent need to improve the SOA modeling in climate models. © 2021 Copernicus GmbH. All rights reserved. |
语种 | 英语 |
scopus关键词 | aerosol formation; annual variation; atmospheric chemistry; climate modeling; concentration (composition); seasonal variation; stratosphere; troposphere |
来源期刊 | ATMOSPHERIC CHEMISTRY AND PHYSICS
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文献类型 | 期刊论文 |
条目标识符 | http://gcip.llas.ac.cn/handle/2XKMVOVA/246862 |
作者单位 | School of Atmospheric Science, Nanjing University, Nanjing, China; Joint International Research Laboratory of Atmospheric and Earth System Sciences, Institute for Climate and Global Change Research, Nanjing University, China; National Center for Atmospheric Research, Boulder, CO, United States; Pacific Northwest National Laboratory, Richland, WA, United States |
推荐引用方式 GB/T 7714 | Liu Y.,Dong X.,Wang M.,et al. Analysis of secondary organic aerosol simulation bias in the Community Earth System Model (CESM2.1)[J],2021,21(10). |
APA | Liu Y..,Dong X..,Wang M..,Emmons L.K..,Liu Y..,...&Shrivastava M..(2021).Analysis of secondary organic aerosol simulation bias in the Community Earth System Model (CESM2.1).ATMOSPHERIC CHEMISTRY AND PHYSICS,21(10). |
MLA | Liu Y.,et al."Analysis of secondary organic aerosol simulation bias in the Community Earth System Model (CESM2.1)".ATMOSPHERIC CHEMISTRY AND PHYSICS 21.10(2021). |
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