ABSTRACT
Intensive measurements were conducted in Xi’an, China before and during a COVID-19 lockdown period to investigate how changes in anthropogenic emissions affected the optical properties and radiative effects of brown carbon (BrC) aerosol. The contribution of BrC to total aerosol light absorption during the lockdown (13%–49%) was higher compared with the normal period (4%–29%). Mass absorption cross-sections (MAC) of specific organic aerosol (OA) factors were calculated from a ridge regression model. Of the primary OA (POA), coal combustion OA (CCOA) had the largest MACs at all tested wavelengths during both periods due to high molecular-weight BrC chromophores;that was followed by biomass burning OA (BBOA) and hydrocarbon-like OA (HOA). For secondary OA (SOA), the MACs of the less-oxidized oxygenated OA (OOA) species (LO-OOA) at λ = 370–590 nm were higher than those of more-oxidized OOA (MO-OOA) during both periods, presumably due to chromophore bleaching. The largest contributor to BrC absorption at the short wavelengths was CCOA during both periods, but BrC absorption by LO-OOA and MO-OOA became dominant at longer wavelengths during the lockdown. The estimated radiation forcing efficiency of BrC over 370–600 nm increased from 37.5 W· g-1 during the normal period to 50.2 W·g-1 during the lockdown, and that enhancement was mainly caused by higher MACs for both LO-OOA and MO-OOA. This study provides insights into the optical properties and radiative effects of source-specific BrC aerosol when pollution emissions are reduced.
ABSTRACT
Restrictions on human activities were implemented in China to cope with the outbreak of the Coronavirus Disease 2019 (COVID-19), providing an opportunity to investigate the impacts of anthropogenic emissions on air quality. Intensive real-time measurements were made to compare primary emissions and secondary aerosol formation in Xi'an, China before and during the COVID-19 lockdown. Decreases in mass concentrations of particulate matter (PM) and its components were observed during the lockdown with reductions of 32-51%. The dominant contributor of PM was organic aerosol (OA), and results of a hybrid environmental receptor model indicated OA was composed of four primary OA (POA) factors (hydrocarbon-like OA (HOA), cooking OA (COA), biomass burning OA (BBOA), and coal combustion OA (CCOA)) and two oxygenated OA (OOA) factors (less-oxidized OOA (LO-OOA) and more-oxidized OOA (MO-OOA)). The mass concentrations of OA factors decreased from before to during the lockdown over a range of 17% to 58%, and they were affected by control measures and secondary processes. Correlations of secondary aerosols/ΔCO with Ox (NO2 + O3) and aerosol liquid water content indicated that photochemical oxidation had a greater effect on the formation of nitrate and two OOAs than sulfate; however, aqueous-phase reaction presented a more complex effect on secondary aerosols formation at different relative humidity condition. The formation efficiencies of secondary aerosols were enhanced during the lockdown as the increase of atmospheric oxidation capacity. Analyses of pollution episodes highlighted the importance of OA, especially the LO-OOA, for air pollution during the lockdown.