Improvement of inorganic aerosol component in PM2.5 by constraining aqueous-phase formation of sulfate in cloud with satellite retrievals: WRF-Chem simulations

被引:11
|
作者
Sha, Tong [1 ]
Ma, Xiaoyan [1 ]
Wang, Jun [2 ]
Tian, Rong [1 ]
Zhao, Jianqi [1 ]
Cao, Fang [3 ,4 ,5 ]
Zhang, Yan-Lin [3 ,4 ,5 ]
机构
[1] Nanjing Univ Informat Sci & Technol, Collaborat Innovat Ctr Forecast & Evaluat Meteoro, Key Lab Aerosol Cloud Precipitat China Meteorol A, Nanjing 210044, Peoples R China
[2] Univ Iowa, Ctr Global & Reg Environm Res, Dept Chem & Biochem Engn, Iowa City, IA 52242 USA
[3] Nanjing Univ Informat Sci & Technol, Coll Appl Meteorol, Yale NULST Ctr Atmospher Environm, Int Joint Lab Climate & Environm Change, Nanjing 210044, Peoples R China
[4] Nanjing Univ Informat Sci & Technol, Coll Appl Meteorol, Key Lab Meteorol Disaster, Minist Educ, Nanjing 210044, Peoples R China
[5] Nanjing Univ Informat Sci & Technol, Coll Appl Meteorol, Collaborat Innovat Ctr Forecast & Evaluat Meteoro, Jiangsu Prov Key Lab Agr Meteorol, Nanjing 210044, Peoples R China
基金
中国国家自然科学基金;
关键词
Sulfate; Aqueous-phase chemistry; Cloud water; WRF-Chem; Satellite data; COMMUNITY CLIMATE MODEL; MICS-ASIA III; HAZE EVENTS; AIR-QUALITY; HETEROGENEOUS CHEMISTRY; BOUNDARY-LAYER; WINTER HAZE; FORMATION MECHANISMS; NIGHTTIME CHEMISTRY; NATIONAL CENTER;
D O I
10.1016/j.scitotenv.2021.150229
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
High concentrations of PM2.5 in China have caused severe visibility degradation and health problems. However, it is still challenging to accurately predict PM2.5 and its chemical components in numerical models. In this study, we compared the inorganic aerosol components of PM2.5 (sulfate, nitrate, and ammonium (SNA)) simulated by the Weather Research and Forecasting model fully coupled with chemistry (WRF-Chem) model with in-situ data in a heavy haze-fog event during November 2018 in Nanjing, China. Comparisons show that the model underesti-mates sulfate concentrations by 81% and fails to reproduce the significant increase of sulfate from early morning to noon, which corresponds to the timing of fog dissipation that suggests the model underestimates the aqueous-phase formation of sulfate in clouds. In addition, the model overestimates both nitrate and ammonium concen-trations by 184% and 57%, respectively. These overestimates contribute to the simulated SNA being 77.2% higher than observed. However, cloud water content is also underestimated which is a pathway for important aqueous-phase reactions. Therefore, we constrained the simulated cloud water content based on the Moderate Resolution Imaging Spectroradiometer (MODIS) Liquid Water Path observations. Results show that the simulation with MODIS-corrected cloud water content increases the sulfate by a factor of 3, decreases the Normalized Mean Bias (NMB) by 53.5%, and reproduces its diurnal cycle with the peak concentration occurring at noon. The im -proved sulfate simulation also improves the simulation of nitrate, which decreases the simulated nitrate bias by 134%. Although the simulated ammonium is still higher than the observations, corrected cloud water content leads to a decrease of the modelled bias in SNA from 77.2% to 14.1%. The strong sensitivity of simulated SNA concentration to the cloud water content provides an explanation for the simulated SNA bias. Hence, uncertainties in cloud water content can contribute to model biases in simulating SNA which are less frequently explored from a process-level perspective and can be reduced by constraining the model with satellite observations. (C) 2021 Elsevier B.V. All rights reserved.
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页数:13
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