Abstract. We analyzed the measurements of ozone (O3) and its precursors made at rural/suburban sites downwind of four large Chinese cities – Beijing, Shanghai, Guangzhou and Lanzhou, to elucidate their pollution characteristics, regional transport, in situ production, and impacts of heterogeneous processes. The same measurement techniques and observation-based model were used to minimize uncertainties in comparison of the results due to difference in methodologies. All four cities suffered from serious O3 pollution but showed different precursor distributions. The model-calculated in situ O3 production rates were compared with the observed change rates to infer the relative contributions of on-site photochemistry and transport. At the rural site downwind of Beijing, export of the well-processed urban plumes contributed to the extremely high O3 levels (up to an hourly value of 286 ppbv), while the O3 pollution observed at suburban sites of Shanghai, Guangzhou and Lanzhou was dominated by intense in situ production. The O3 production was in a volatile organic compound (VOC)-limited regime in both Shanghai and Guangzhou, and a NOx-limited regime in Lanzhou. The key VOC precursors are aromatics and alkenes in Shanghai, and aromatics in Guangzhou. The potential impacts on O3 production of several heterogeneous processes, namely, hydrolysis of dinitrogen pentoxide (N2O5), uptake of hydro peroxy radical (HO2) on particles and surface reactions of NO2 forming nitrous acid (HONO), were assessed. The analyses indicate the varying and considerable impacts of these processes in different areas of China depending on the atmospheric abundances of aerosol and NOx, and suggest the urgent need to better understand these processes and represent them in photochemical models.

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[1] Surface ozone (O 3 ), carbon monoxide (CO), and total and speciated reactive nitrogen compounds (NO y , NO, NO 2 , PAN, HNO 3 , and particulate NO 3 − ) were measured at Mount Waliguan (WLG; 36.28°N, 100.90°E, 3816 m above sea level (asl)) in the summer of 2006 to further understand the sources of ozone and reactive nitrogen and to investigate the partitioning of reactive nitrogen over the remote Qinghai-Tibetan Plateau. The mean mixing ratios of O 3 , CO, NO y , and daytime NO were 59 ppbv, 149 ppbv, 1.44 ppbv, and 71 pptv, respectively, which (except for NO y ) were higher than those measured from a previous campaign in summer 2003, which is consistent with more frequent transport of anthropogenic pollution from central and eastern China in the measurement period of 2006 (55%) than that of 2003 (25%). The abnormally high values of NO y observed in 2003 were suspected to be due to the positive interference from ammonia (NH 3 ) to the particular catalytic converter used in that study. Varied diurnal patterns were observed for the various NO y components. The ozone production efficiencies (DO 3 /DNO z ), which were estimated from the slope of the O 3 -NO z scatterplot, were 7.7-11.3 for the polluted plumes from central and eastern China. The speciation of reactive nitrogen was investigated for the first time in the remote free troposphere in western China. PAN and particulate NO 3 − were the most abundant reactive nitrogen species at WLG, with average proportions of 32% and 31%, followed by NO x (24%) and HNO 3 (20%). The relatively large contribution of particulate NO 3 − to NO y was due to the presence of high concentrations of NH 3 and crustal particles, which favor the formation of particulate nitrate. An analysis of backward trajectories for the recent 10 years revealed that air masses from central and eastern China dominated the airflow at WLG in summer, suggesting strong impact of anthropogenic forcing on the surface ozone and other trace constituents on the Plateau.

Abstract. We analyzed measurements of ozone (O3) and its precursors made at rural/suburban sites downwind of four large Chinese cities – Beijing, Shanghai, Guangzhou and Lanzhou, to elucidate their pollution characteristics, regional transport, in situ production, and impacts of heterogeneous processes. The same measurement techniques and observation-based model were used to minimize uncertainties in comparison of the results due to difference in methodologies. All four cities suffered from serious O3 pollution but showed different precursor distributions. The model-calculated in situ O3 production rates were compared with the observed change rates to infer the relative contributions of on-site photochemistry and transport. At the rural site of Beijing, export of the well-processed urban plumes contributed to the extremely high O3 levels (up to an hourly value of 286 ppbv), while the O3 pollution observed at suburban sites of Shanghai, Guangzhou and Lanzhou was dominated by intense in-situ production. The O3 production was in a VOCs-limited regime in both Shanghai and Guangzhou, and a NOx-controlled regime in Lanzhou. The key VOC precursors are aromatics and alkenes in Shanghai, and aromatics in Guangzhou. The potential impacts on O3 production of several heterogeneous processes, namely, hydrolysis of dinitrogen pentoxide (N2O5), uptake of hydro peroxy radical (HO2) on particles and surface reactions of NO2 forming nitrous acid (HONO), were assessed. The analyses indicate the varying and considerable impacts of these processes in different areas of China depending on the atmospheric abundances of aerosol and NOx, and suggest the urgent need to better understand these processes and represent them in photochemical models.