On the basis of three mountain sites (Mount Tai, Hua and Huang) newly founded in east‐central China and several other sites from the Acid Deposition Monitoring Network in east Asia (EANET) and WMO World Data Centre for Greenhouse Gases (WDCGG), we investigate seasonal cycle of ozone over east Asia and its budgets in east‐central China by using a regional chemical transport model (NAQPMS). The observations show a striking ozone pattern of two sharp peaks in May‐June and September–October at three mountain sites in east‐central China which are higher than those observed at other mountain sites in Europe and North America. Ozone budgets analysis by the model confirms that maximum of net photochemical productions reaches 31.8, 15.1, and 11.4 ppbv/d at Mount Tai, Hua, and Huang, respectively. The net photochemical production dominates the formation of ozone maximums at Mount Tai and Hua in June, and the importing transport also plays a comparable importance at Mount Huang. In comparison with those in the western North Pacific, east‐central China shows stronger net photochemical productions, which are comparable to anthropogenic sources regions in Europe and North America.
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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