Mercury stable isotope compositions of Chinese urban fine particulates in winter haze days: Implications for Hg sources and transformations

Atmospheric pollution by fine particulates and mercury (Hg) in emerging economies is a serious environmental concern. Here, we present Hg concentrations and isotope compositions of 24-hour integrated fine particulate matter (PM2.5) samples collected during January 2014 at four large Chinese cities (three inland cities: Beijing, Changchun and Chengdu; one coastal city: Hong Kong), with an aim of identifying the potential Hg sources and transformation processes. Mean concentrations of PM2.5 (171 ± 62 μg m−3) and PM2.5-bound Hg (1.3 ± 1.1 ng m−3) in Chengdu were the highest. Overall, PM2.5 samples in Chinese inland cities were characterized by moderately negative δ202Hg (−1.08 ± 0.64‰, 1σ), slightly negative Δ199Hg (−0.13 ± 0.28‰, 1σ) and insignificant Δ200Hg (0.03 ± 0.05‰, 1σ). On average, δ202Hg of PM2.5 was the highest in Chengdu (−0.74 ± 0.67‰, 1σ), followed by Beijing (−1.11 ± 0.26‰, 1σ) and Changchun (−1.60 ± 0.45‰, 1σ). PM2.5 from Beijing showed the most negative Δ199Hg (−0.31 ± 0.40‰, 1σ) that was significantly lower than Changchun (−0.12 ± 0.21‰, 1σ) and Chengdu (−0.02 ± 0.15‰, 1σ). Coal combustion and cement production were identified to be the dominant sources of PM2.5-bound Hg in these cities, with additional Hg sources from non-ferrous metal smelting in Chengdu. Besides, Hg emissions from biomass burning were evident in specific days for each city. We found that source materials and isotope fractionation during emission processes could not fully explain the observed Hg isotope compositions in PM2.5, especially the large negative Δ199Hg values (<−0.3‰) in Beijing. The near-unity slope of Δ199Hg vs. Δ201Hg in PM2.5 samples from each studied city indicates that HgII in the fine aerosols was likely photo-reduced to different degrees in the atmosphere following emission from sources.