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Severe wintertime PM 2.5 pollution in Beijing has been receiving increasing worldwide attention, yet the decadal variations remain relatively unexplored. Combining field measurements and model simulations, we quantified the relative influences of anthropogenic emissions and meteorological conditions on PM 2.5 concentrations in Beijing over the winters of 2002–2016. Between the winters of 2011 and 2016, stringent emission control measures resulted in a 21 % decrease in mean mass concentrations of PM 2.5 in Beijing, with 7 fewer haze days per winter on average. Given the overestimation of PM 2.5 by the model, the effectiveness of stringent emission control measures might have been slightly overstated. With fixed emissions, meteorological conditions over the study period would have led to an increase in haze in Beijing, but the strict emission control measures have suppressed the unfavorable influences of the recent climate. The unfavorable meteorological conditions are attributed to the weakening of the East Asia winter monsoon associated particularly with an increase in pressure associated with the Aleutian Low. [ABSTRACT FROM AUTHOR]

We examine seasonal variations of carbon monoxide (CO), ozone (O3), and their relationships observed over the course of 3 yr (2005–2007) at Miyun, a rural site 100 km north of Beijing. Monthly mean afternoon mixing ratios of CO have broad maxima in winter and a secondary peak in June. Monthly mean afternoon O3 shows a clear seasonal pattern with a major peak in June (85 ppb), a secondary peak in September (65 ppb) and minimum in winter (50–55 ppb). The seasonal cycles of O3 and CO are associated with seasonal changes in dominant synoptic pattern. Substantial interannual variability is found for CO which is attributed to the interannual variability of meteorology and emissions from biomass burning. The seasonality and magnitude of background CO and O3 derived at Miyun are consistent with observations at upwind remote continental sites. The O3–CO correlation slope is about 0.07 ppb ppb−1 on average in summer, significantly lower than the typical slope of 0.3 ppb ppb−1 reported for developed countries. The O3–CO correlation slope shows large gradients for different types of air masses (0.133 ± 0.017 ppb ppb−1 in aged urban pollution plumes and 0.047 ± 0.008 ppb ppb−1 in biomass burning plumes), suggesting that the conventional method of direct scaling the mean O3–CO slope by CO emissions to deduce O3 production rate is subject to large uncertainties if applied for China. [ABSTRACT FROM AUTHOR]