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As a potent climate forcer, black carbon (BC) optical properties can have significant impacts on the regional meteorology and climate. To unveil the seasonal differences of BC and its contribution by various emission sources, a one-year continuous monitoring of atmospheric aerosols was conducted at a background coastal site in Eastern China. By comparing the seasonal and diurnal patterns between BC and elemental carbon, we observed that BC were evidently aged with varying extents among all four seasons. The light absorption enhancement of BC (E abs ) was calculated as 1.89 ± 0.46, 2.40 ± 0.69, 1.91 ± 0.60, and 1.34 ± 0.28, from spring to winter, respectively, indicating that BC was more aged in summer. Contrary to the negligible impact of pollution levels on E abs , the patterns of air masses arriving to the sampling site had a significant impact on the seasonal optical characteristics of BC. Sea breezes evidently exhibited higher E abs than land-sourced breezes, and BC was more aged and light-absorbing with an increased contribution of marine airflows. By applying a receptor model, we resolved six emission sources as ship emission, traffic emission, secondary pollution, coal combustion, sea salt, and mineral dust. The mass absorption efficiency of BC for each source was estimated, showing the highest from the ship emission sector. This explained the highest E abs observed in summer and sea breezes. Our study highlights that curbing emission from shipping activities is beneficial for reducing the warming effect of BC in coastal areas, particularly in the context of future rapid development of international shipping., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier B.V.)

The coronavirus (COVID-19) pandemic is disrupting the world from many aspects. In this study, the impact of emission variations on PM 2.5 -bound elemental species and health risks associated to inhalation exposure has been analyzed based on real-time measurements at a remote coastal site in Shanghai during the pandemic. Most trace elemental species decreased significantly and displayed almost no diel peaks during the lockdown. After the lockdown, they rebounded rapidly, of which V and Ni even exceeded the levels before the lockdown, suggesting the recovery of both inland and shipping activities. Five sources were identified based on receptor modeling. Coal combustion accounted for more than 70% of the measured elemental concentrations before and during the lockdown. Shipping emissions, fugitive/mineral dust, and waste incineration all showed elevated contributions after the lockdown. The total non-carcinogenic risk (HQ) for the target elements exceeded the risk threshold for both children and adults with chloride as the predominant species contributing to HQ. Whereas, the total carcinogenic risk (TR) for adults was above the acceptable level and much higher than that for children. Waste incineration was the largest contributor to HQ, while manufacture processing and coal combustion were the main sources of TR. Lockdown control measures were beneficial for lowering the carcinogenic risk while unexpectedly increased the non-carcinogenic risk. From the perspective of health effects, priorities of control measures should be given to waste incineration, manufacture processing, and coal combustion. A balanced way should be reached between both lowering the levels of air pollutants and their health risks., (Copyright © 2021. Published by Elsevier B.V.)

The wide spread of the coronavirus (COVID-19) has significantly impacted the global human activities. Compared to numerous studies on conventional air pollutants, atmospheric mercury that has matched sources from both anthropogenic and natural emissions is rarely investigated. At a regional site in eastern China, an intensive measurement was performed, showing obvious decreases in gaseous elemental mercury (GEM) during the COVID-19 lockdown, while it was not as significant as most of the other measured air pollutants. Before the lockdown, when anthropogenic emissions dominated, GEM showed no correlation with temperature and negative correlations with wind speed and the height of the boundary layer. In contrast, GEM showed significant correlation with temperature, while the relationship between GEM and the wind speed/boundary layer disappeared during the lockdown, suggesting the enhanced natural emissions of mercury. By applying a machine learning model and the SHAP (SHapley Additive exPlanations) approach, it was found that the mercury pollution episodes before the lockdown were driven by anthropogenic sources, while they were mainly driven by natural sources during and after the lockdown. Source apportionment results showed that the absolute contribution of natural surface emissions to GEM unexpectedly increased (44 %) during the lockdown. Throughout the whole study period, a significant negative correlation was observed between the absolute contribution of natural and anthropogenic sources to GEM. We conclude that the natural release of mercury could be stimulated to compensate for the significantly reduced anthropogenic GEM via the surface–air exchange in the balance of mercury. [ABSTRACT FROM AUTHOR]

Sea salts act as an important medium for atmospheric processing. One intensive field campaign in the September–October period of 2019 was conducted at a subtropical coastal site over the South China Sea. Unexpected high concentrations of acidic gaseous precursors were observed, yielding high sulfate in PM2.5. Na+ ranked as the third highest inorganic species, about half of NH4+. Significant cation deficiency was found due to the ammonia‐poor environment. Diel patterns of most air pollutants from land breeze were stronger than that from marine breeze and presented pronounced unimodal distributions, which were ascribed to complex chemical processing mixed with regional transport. Thermodynamic equilibrium model (ISORROPIA II) simulation revealed sea salts could be internally mixed with fine particle secondary species and suggested evident multiphase reactions on sea salts. The simulated aerosol pH reached as low as 1.63 ± 0.50, which was related to high sulfate, insufficient alkaline species, and low aerosol liquid water content. During a continuous sea breeze episode, SO42− was underpredicted by 2.89 ± 3.85 μg m−3 if Na+ was not considered in ISORROPIA simulation. The retrieved Na+ ‐related ion pairs (NaCl, NaHSO4, and Na2SO4) accounted for about one‐fourth of the total inorganic aerosols. This study highlighted that intense atmospheric processing on sea salts occurred in fine particles and the mixing state between sea salts and other aerosol species should be considered in aerosol acidity prediction and secondary aerosol formation in coastal regions. Key Points: Sea salts were internally mixed with the secondary species even in fine particle, suggesting evident multiphase reactions on sea saltsAerosol pH was very low at the land‐sea interface and it depended on the relative strengths of sea salts versus terrestrial ammonia emissionsThe retrieved chemical forms of SO42− contained a substantial contribution from bisulfate, mainly in the form of NaHSO4 and NH4HSO4 [ABSTRACT FROM AUTHOR]

To evaluate the effect of temporary emission control measures on air quality during the 2016 G20 summit held in Hangzhou, China, an intensive field campaign was conducted with a focus on aerosol chemistry and gaseous precursors from 15 August to 12 September 2016. The concentrations of fine particles were reduced during the intense emission control stages, with the reduction of carbonaceous matter being mostly responsible for this observed decrease. This, in turn, was mainly ascribed to the decrease of secondary organic aerosols via the suppression of daytime peak secondary organic carbon (SOC)formation. Although the regional joint control was enacted extending to the Yangtze River Delta region, the effect of long-range transport on the air quality of Hangzhou was ubiquitous. Unexpectedly high NOx concentrations were observed during the control stage, when the strictest restriction on vehicles was implemented, owing to contributions from upstream populous regions such as Jiangsu and Shandong provinces. In addition, the continental outflow traveling over the ocean triggered a short pollution episode on the first day of the G20 summit, resulting in a significant enhancement of the nitrogen/sulfur oxidation rates. In the wake of the summit, all air pollutants evidently rebounded after the various control measures were lifted. Overall, the fraction of secondary inorganic aerosols (SIA; in this case sulfate, nitrate, and ammonium aerosols -- SNA) in PM2:5 increased as relative humidity increased; however, the overall concentration of PM2:5 did not increase. To evaluate the effect of temporary emission control measures on air quality during the 2016 G20 summit held in Hangzhou, China, an intensive field campaign was conducted with a focus on aerosol chemistry and gaseous precursors from 15 August to 12 September 2016. The concentrations of fine particles were reduced during the intense emission control stages, with the reduction of carbonaceous matter being mostly responsible for this observed decrease. This, in turn, was mainly ascribed to the decrease of secondary organic aerosols via the suppression of daytime peak secondary organic carbon (SOC)formation. Although the regional joint control was enacted extending to the Yangtze River Delta region, the effect of long-range transport on the air quality of Hangzhou was ubiquitous. Unexpectedly high NOx concentrations were observed during the control stage, when the strictest restriction on vehicles was implemented, owing to contributions from upstream populous regions such as Jiangsu and Shandong provinces. In addition, the continental outflow traveling over the ocean triggered a short pollution episode on the first day of the G20 summit, resulting in a significant enhancement of the nitrogen/sulfur oxidation rates. In the wake of the summit, all air pollutants evidently rebounded after the various control measures were lifted. Overall, the fraction of secondary inorganic aerosols (SIA; in this case sulfate, nitrate, and ammonium aerosols -- SNA) in PM2:5 increased as relative humidity increased; however, the overall concentration of PM2:5 did not increase. [ABSTRACT FROM AUTHOR]