Atmospheric chemistry and physics · 2016 · 26 citations · 75 references
Natural SciencesChemistryEarth SciencesAir-sea InteractionAtmospheric ChemistryAtmospheric ScienceAerosol ChemistryAerosol PhysicsAerosol ScienceAtmospheric CompositionParticulate MatterSecondary Aerosol FormationAerosol Chemical CompositionAtmospheric Aerosol ChemistryAtmospheric Nitrate FormationAtmospheric Transport ModelingChloride DepletionNew Particle FormationNitrate AerosolsSea-salt Aerosols
Abstract. Measurements of size-resolved aerosols from 0.25 to 18 µm were conducted at three sites (urban, suburban and background sites) and used in tandem with an atmospheric transport model to study the size distribution and formation of atmospheric aerosols in southern China during the monsoon season (May–June) in 2010. The mass distribution showed the majority of chemical components were found in the smaller size bins (< 2.5 µm). Sulfate was found to be strongly correlated with aerosol water and anticorrelated with atmospheric SO2, hinting at aqueous-phase reactions being the main formation pathway. Nitrate was the only major species that showed a bimodal distribution at the urban site and was dominated by the coarse mode in the other two sites, suggesting that an important component of nitrate formation is chloride depletion of sea salt transported from the South China Sea. In addition to these aqueous-phase reactions and interactions with sea salt aerosols, new particle formation, chemical aging, and long-range transport from upwind urban or biomass burning regions was also found to be important in at least some of the sites on some of the days. This work therefore summarizes the different mechanisms that significantly impact the aerosol chemical composition during the monsoon over southern China.
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