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Abstract: To improve the air quality during the 2008 Beijing Olympic Games, the Beijing Municipal Government enforced a series of emission control measures. This provided a valuable case study to evaluate the effectiveness of these aggressive measures on mitigating air pollution and improving the atmospheric environment. In this paper, we report the first results of the chemical and Sr isotopic compositions of the rainwater in Beijing during the 2008 Olympic year. The ionic composition of samples show that Ca2+ and NH4 + were the dominant cations, accounting for about 76–97% of the total cations, and that SO4 2− and NO3 − were the major anions, accounting for 61–91% of the total anions measured. Using Na as the indicator of marine origin and Al as that of terrestrial inputs, the proportions of sea salt and terrestrial elements were estimated from elemental ratios. The calculated results indicate that the major chemical components were mainly of non-sea-salt origin. Good correlation between Ca2+ and Sr2+ (R 2 =0.85) in rainwater samples indicates the potential of Sr as a provenance tracer for Ca. Sr2+ concentrations in rainwater samples ranged from 0.01 to 2.87μmoll−1, with 87Sr/86Sr ratios from 0.7092 to 0.7109. All of the samples had a 87Sr/86Sr ratio higher than that of seawater. The 87Sr/86Sr isotopic and elemental ratio systems show that the data set of rainwater was mainly distributed between the seawater end-member (~0.70917) and the soil dust end-member (0.7111–0.7115), and the analysis indicate that the effect of anthropogenic inputs could decrease in 2008. Comparisons of the chemical composition of the rainwater in different periods show that all chemical components, except NH4 +, had the lowest concentration levels during the Olympic Game period. The VWM concentrations of major ions in the rainwater decreased significantly during the Olympic period by up to 29% for SO4 2−, 39% for NO3 −, 38% for Ca2+, 51% for Mg2+, 57% for K+, and 44% for Na+, compared with the pre-control period. The concentrations of almost all species decreased during the 2008 Olympics, most likely due to both strict emission controls and favorable meteorological conditions. [Copyright &y& Elsevier]

In this paper, we report the results and analysis of a recent field campaign in August 2007 investigating the impacts of emissions from transportation on air quality and community concentrations in Beijing, China. We conducted measurements in three different environments, on-road, roadside and ambient. The carbon monoxide, black carbon and ultrafine particle number emission factors for on-road light-duty vehicles are derived to be 95gkg−1-fuel, 0.3gkg−1-fuel and 1.8×1015 particleskg−1-fuel, respectively. The emission factors for on-road heavy-duty vehicles are 50gkg−1-fuel, 1.3gkg−1-fuel and 1.1×1016 particleskg−1-fuel, respectively. The carbon monoxide emission factors from this study agree with those derived from remote sensing and on-board vehicle emission testing systems in China. The on-road black carbon and particle number emission factors for Chinese vehicles are reported for the first time in the literature. Strong traffic impacts can be observed from the concentrations measured in these different environments. Most clear is a reflection of diesel truck traffic activity in black carbon concentrations. The comparison of the particle size distributions measured at the three environments suggests that the traffic is a major source of ultrafine particles. A four-day traffic control experiment conducted by the Beijing Government as a pilot to test the effectiveness of proposed controls was found to be effective in reducing extreme concentrations that occurred at both on-road and ambient environments. [Copyright &y& Elsevier]

This paper presents a novel method for quantification of the total emission of gases from area sources using the mobile mini-DOAS (Differential Optical Absorption Spectroscopy) instrument, a ground based optical remote sensing technique. The presented method has been applied to measure the emission of SO2 and NO2 from the city of Beijing, P.R. China, on a time scale of approximately 2h. The measurements have been performed during two field campaigns, in April and in August 2005. The estimated emission of NO2 is roughly the same during the two field campaigns with an average emission of 189tonsd−1 during April and 174tonsd−1 during August. The estimated emission of SO2 varies greatly between the two periods, with an average emission of 293tonsd−1 during April and 52tonsd−1 during August. [Copyright &y& Elsevier]