Abstract. We investigated aerosol hygroscopic growth property and its influence on scattering coefficient using M9003 nephelometers in coupling with humidity controlled inlet system at a rural site near Beijing mega-city from 24 April to 15 May 2006. Inlet relative humidity was controlled in an increasing range of 40%-90% while aerosol hygroscopic growth factor of scattering coefficient, f (RH=80%) as ratio of scattering coefficient at RH=80% to "dry" scattering coefficient (RH<40%) varied in a range of 1.07-2.35 during the measurement. Further analysis indicated that under dust episode, measured f (RH=80%) is 1.2±0.02, and estimated periodic mean value of f (RH=80%) was 1.31±0.03 under clean periods; during urban pollution periods, the aerosol displayed relative strong water absorbing properties with f (RH=80%) of about 1.57±0.02. An examination of chemical composition of daily filter samples highlighted that aerosol hygroscopicity was generally depressed with the increasing ratio of organic matter (OMC)/ammonium sulfate (AS) in particle mass, similar with the results of many previous studies. However, a special case with high value of f (RH=80%)=2.21 and high OMC/AS ratio was also observed, this exception reflected physico-chemical particularities of organic matter and its complex interaction with other compounds during this episode.

Abstract. An online air pollutant tagged module has been developed in the Nested Air Quality Prediction Model System (NAQPMS) to investigate the impact of local and regional sources on the air pollutants in Beijing during the Campaign of Air Quality Research in Beijing 2006(CAREBeijing-2006). The NAQPMS model shows high performance in simulating sulfur dioxide (SO 2 ), particulate matter (PM 10 ), nitrogen dioxide (NO 2 ), and ozone (O 3 ) with overall better agreements with the observations at urban sites than rural areas. With the tagged module, the air pollutant contributions from local and regional sources to the surface layer (about 30 m) and the upper layer (about 1.1 km) in Beijing are differentiated and estimated. The air pollutants at the surface layer in Beijing are dominated by the contributions from local sources, accounting for 65 % of SO 2 , 75 % of PM 10 and nearly 90 % of NO 2 , respectively, comparatively, the 1.1 km layer has large source contributions from the surrounding regions (e.g., southern Beijing), accounting for more than 50 % of the SO 2 and PM 10 concentrations. County scale analysis is also performed and the results suggest that Tianjin is the dominant source of SO 2 in Pinggu County, and Langfang, Hebei is the most important regional contributor to PM 10 in Beijing. Moreover, the surrounding regions show larger impact on SO 2 , PM 10 and NO 2 in the eastern counties of Beijing (e.g., Pinggu, Tongzhou and Daxing) than those in western Beijing, which is likely due to the Beijing's semi-basin topography and the summer monsoon. Our results indicate that the efforts to control the air pollutants in Beijing should focus on controlling both local and regional emissions.

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