In January 2020, anthropogenic emissions in Northeast Asia reduced due to the COVID-19 outbreak. When outdoor activities of the public were limited, PM2.5 concentrations in China and South Korea between February and March 2020 reduced by − 16.8 μg/m3 and − 9.9 μg/m3 respectively, compared with the average over the previous three years. This study uses air quality modeling and observations over the past four years to separate the influence of reductions in anthropogenic emissions from meteorological changes and emission control policies on this PM2.5 concentration change. Here, we show that the impacts of anthropogenic pollution reduction on PM2.5 were found to be approximately − 16% in China and − 21% in South Korea, while those of meteorology and emission policies were − 7% and − 8% in China, and − 5% and − 4% in South Korea, respectively. These results show that the influence on PM2.5 concentration differs across time and region and according to meteorological conditions and emission control policies. Finally, the influence of reductions in anthropogenic emissions was greater than that of meteorological conditions and emission policies during COVID-19 period.

Abstract. The prediction of secondary organic aerosol (SOA) on regional scales is traditionally performed by using gas–particle partitioning models. In the presence of inorganic salted wet aerosols, aqueous reactions of semivolatile organic compounds can also significantly contribute to SOA formation. The UNIfied Partitioning-Aerosol phase Reaction (UNIPAR) model utilizes the explicit gas mechanism to better predict SOA formation from multiphase reactions of hydrocarbons. In this work, the UNIPAR model was incorporated with the Comprehensive Air Quality Model with Extensions (CAMx) to predict the ambient concentration of organic matter (OM) in urban atmospheres during the Korean-United States Air Quality (2016 KORUS-AQ) campaign. The SOA mass predicted with CAMx–UNIPAR changed with varying levels of humidity and emissions and in turn has the potential to improve the accuracy of OM simulations. CAMx–UNIPAR significantly improved the simulation of SOA formation under the wet condition, which often occurred during the KORUS-AQ campaign, through the consideration of aqueous reactions of reactive organic species and gas–aqueous partitioning. The contribution of aromatic SOA to total OM was significant during the low-level transport/haze period (24–31 May 2016) because aromatic oxygenated products are hydrophilic and reactive in aqueous aerosols. The OM mass predicted with CAMx–UNIPAR was compared with that predicted with CAMx integrated with the conventional two-product model (SOAP). Based on estimated statistical parameters to predict OM mass, the performance of CAMx–UNIPAR was noticeably better than that of the conventional CAMx model, although both SOA models underestimated OM compared to observed values, possibly due to missing precursor hydrocarbons such as sesquiterpenes, alkanes, and intermediate volatile organic compounds (VOCs). The CAMx–UNIPAR simulation suggested that in the urban areas of South Korea, terpene and anthropogenic emissions significantly contribute to SOA formation while isoprene SOA minimally impacts SOA formation.

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