Variability of submicron aerosol observed at a rural site in Beijing in the summer of 2006

Ground‐based measurements of aerosol and trace gases were conducted at a rural site in Beijing in the summer of 2006 as a part of the Campaigns of Air Quality Research in Beijing and Surrounding Region 2006 (CAREBeijing 2006). The size‐resolved chemical composition of submicron aerosol was measured using an Aerodyne quadrupole aerosol mass spectrometer (AMS). The data obtained from 15 August to 10 September 2006 are presented. Meteorological analysis shows that the measurement period can be characterized as a cycle of low wind speed periods over the course of a few days (stagnant periods) followed by rapid advection of clean air from the north/northwest mostly due to passage of a midlatitude cyclone. Mass concentrations of total measured aerosol with diameters less than 1 μ m (total PM 1 ), which is defined as the sum of elemental carbon and nonrefractory components measured by the AMS, were highly variable, ranging from ∼2 to ∼100 μ g m −3 . Large variability of the PM 1 composition and drastic changes in the sulfate (SO 4 2− ) size distribution were observed to be associated with the cycle of stagnant periods and advection of clean air, indicating that both chemical and physical properties of aerosols were significantly altered on a time scale of a few days. We have found the dominance of organic aerosol at lower total PM 1 mass loadings and that of SO 4 2− at higher mass loadings, which may have important implications for the PM control strategy in Beijing. Possible factors affecting the evolution of the mass concentration and size distribution of SO 4 2− are discussed.