The variation characteristics and possible sources of atmospheric water-soluble ions in Beijing
Abstract. The North China plain (NCP) including Beijing is currently suffering from severe haze events due to high pollution level of atmospheric fine particles called PM2.5. To mitigate the serious pollution status, identification of the sources of PM2.5 is urgently needed for the effective control measures. A total of 235 daily samples of PM2.5 were collected in Beijing through the year of 2014, and the variation characteristics of water-soluble ions (WSIs) in the PM2.5 were comprehensively analyzed for recognizing their possible sources. The results indicated that the periodic emissions from farmers' activities made evident contribution to the atmospheric WSIs in Beijing. The unusually high ratio of Cl− to Na+ in summer could be rationally explained by the prevailing fertilization of NH4Cl for planting summer maize in the vast area of NCP. The remarkable elevation of Cl− in winter was ascribed to coal combustion for heating by farmers. The most serious pollution episodes in autumn were coincident with significant elevation of Ca2+ which was ascribed to be from harvest of the summer maize and tillage for planting the winter wheat. The mineral dust emission from the harvest and tillage not only increased the atmospheric concentrations of the primary pollutants, but also greatly accelerated formation of sulfate and nitrate through heterogeneous reactions of NO2 and SO2 on the mineral dust. The relatively high concentration of K+ in winter and autumn further confirmed that crop straw burning made evident contribution to atmospheric PM2.5 in Beijing. The backward trajectories also indicated that the highest concentrations of WSIs usually occurred in the air parcel from southwest/south regions with high density of farmers. In addition, the values of nitrogen oxidation ratio (NOR) and the sulfur oxidation ratio (SOR) were found to be much higher under haze days than under non-haze days, implying that formation of sulfate and nitrate was greatly accelerated through heterogeneous or multiphase reactions of NO2 and SO2 on PM2.5.