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利用卫星反演约束云相硫酸盐形成来改善 PM 中无机气溶胶成分:WRF-Chem 模拟。

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

机构信息

Collaborative Innovation Center on Forecast and Evaluation of Meteorological Disasters (CIC-FEMD), Key Laboratory for Aerosol-Cloud-Precipitation of China Meteorological Administration, Nanjing University of Information Science & Technology, Nanjing 210044, China.

Collaborative Innovation Center on Forecast and Evaluation of Meteorological Disasters (CIC-FEMD), Key Laboratory for Aerosol-Cloud-Precipitation of China Meteorological Administration, Nanjing University of Information Science & Technology, Nanjing 210044, China.

出版信息

Sci Total Environ. 2022 Jan 15;804:150229. doi: 10.1016/j.scitotenv.2021.150229. Epub 2021 Sep 9.

Abstract

High concentrations of PM in China have caused severe visibility degradation and health problems. However, it is still challenging to accurately predict PM and its chemical components in numerical models. In this study, we compared the inorganic aerosol components of PM (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 underestimates 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 concentrations 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 improved 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.

摘要

中国高浓度的 PM 导致了严重的能见度下降和健康问题。然而,在数值模型中准确预测 PM 和其化学成分仍然具有挑战性。在这项研究中,我们比较了中国 2018 年 11 月南京一次重霾雾事件中,WRF-Chem 模式模拟的大气气溶胶成分(硫酸盐、硝酸盐和铵盐(SNA))与现场数据的差异。结果表明,模型低估了硫酸盐浓度 81%,未能重现硫酸盐从清晨到中午的显著增加,这与雾消散的时间相对应,表明模型低估了云相中硫酸盐的形成。此外,模型高估了硝酸盐和铵盐浓度,分别为 184%和 57%。这些高估导致模拟的 SNA 比观测值高 77.2%。然而,云水量也被低估,这是重要的水相反应途径。因此,我们根据中分辨率成像光谱仪(MODIS)液态水路径观测结果对模拟的云水量进行了约束。结果表明,基于 MODIS 修正的云水量的模拟增加了硫酸盐的浓度,使其增加了 3 倍,归一化平均偏差(NMB)降低了 53.5%,并再现了其日变化规律,峰值浓度出现在中午。硫酸盐模拟的改进也改善了硝酸盐的模拟,使模拟的硝酸盐偏差降低了 134%。尽管模拟的铵盐仍然高于观测值,但修正的云水量导致模型模拟的 SNA 偏差从 77.2%降低到 14.1%。模拟的 SNA 浓度对云水量的强烈敏感性解释了模拟的 SNA 偏差。因此,云水量的不确定性可能导致模型在模拟 SNA 方面存在偏差,这从过程层面的角度来看还较少被探索,通过利用卫星观测结果对模型进行约束,可以减少这种偏差。

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