1Air Quality Studies, Department of Civil and Environmental Engineering, The Hong Kong Polytechnic University, Hong Kong, China
2International Institute for Earth System Science, Nanjing University, Nanjing, China
3Department of Chemistry, University of California at Irvine, California, USA
4School of Atmospheric Sciences, Nanjing University, Nanjing, China
5Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, China
6School of Biomedical, Biomolecular and Chemical Sciences, University of Western Australia, Perth, Australia
Abstract. To advance our understanding on the factors that affect photochemical pollution at different elevations in mountainous areas, concurrent systematic field measurements (September to November 2010) were conducted at a mountain site and at an urban site at the foot of the mountain in Hong Kong. The mixing ratios of air pollutants were greater at the foot of the mountain (i.e., Tsuen Wan urban site, TW) than near the summit (i.e., Tai Mao Shan mountain site, TMS), expect for ozone. In total, only one O3 episode day was observed at TW, whereas twenty-one (21) O3 episode days were observed at TMS. The discrepancy of O3 at the two sites was attributed to the mixed effects of NO titration, vertical meteorological conditions, regional transport and mesoscale circulations. The lower NO levels at TMS and the smaller differences of "oxidant" Ox (O3 + NO2) between the two sites suggested that variations of O3 at the two sites were partly attributed to different degree of NO titration. In addition, analysis of vertical structure of meteorological variables revealed that the inversion layer at the range of altitudes of 500–1000 m might be another factor that caused the high O3 levels at TMS. Furthermore, analyses of the wind fields, the levels of air pollutants in different air flows, ratios of different trace gases and the correlation between variability and the lifetime of VOCs (volatile organic compounds) indicated that high O3 concentrations at TMS were somewhat influenced by regional air masses from the highly polluted Pearl River delta (PRD) region. In particular, the diurnal profiles and correlations of gaseous pollutants suggested influence of mesoscale circulations, which is confirmed using the Master Chemical Mechanism moving box model (Mbox) and the Weather Research and Forecasting (WRF) model. By investigating the correlations of observed O3 and NOx* and the relationships of O3 and its precursors by an observation-based model (OBM), as well as the ratios of VOC/NOx, it was concluded that photochemical O3 formation at TMS was mostly influenced by VOCs, with measurable impact of NOx, while O3 production at TW was generally limited by the concentrations of VOCs. This is the first report of the comprehensive analysis on the data of photochemical pollution obtained from concurrent measurements in mountainous areas in the PRD region.