| Literature DB >> 27485289 |
Ben Yu1,2, Xuewu Fu1, Runsheng Yin1, Hui Zhang1, Xun Wang1,2, Che-Jen Lin1,3, Chuansheng Wu2,4, Yiping Zhang4, Nannan He5, Pingqing Fu5, Zifa Wang5, Lihai Shang1, Jonas Sommar1, Jeroen E Sonke6, Laurence Maurice6, Benjamin Guinot7, Xinbin Feng1.
Abstract
The isotopic composition of atmospheric total gaseous mercury (TGM) and particle-bound mercury (PBM) and mercury (Hg) in litterfall samples have been determined at urban/industrialized and rural sites distributed over mainland China for identifying Hg sources and transformation processes. TGM and PBM near anthropogenic emission sources display negative δ(202)Hg and near-zero Δ(199)Hg in contrast to relatively positive δ(202)Hg and negative Δ(199)Hg observed in remote regions, suggesting that different sources and atmospheric processes force the mass-dependent fractionation (MDF) and mass-independent fractionation (MIF) in the air samples. Both MDF and MIF occur during the uptake of atmospheric Hg by plants, resulting in negative δ(202)Hg and Δ(199)Hg observed in litter-bound Hg. The linear regression resulting from the scatter plot relating the δ(202)Hg to Δ(199)Hg data in the TGM samples indicates distinct anthropogenic or natural influences at the three study sites. A similar trend was also observed for Hg accumulated in broadleaved deciduous forest foliage grown in areas influenced by anthropogenic emissions. The relatively negative MIF in litter-bound Hg compared to TGM is likely a result of the photochemical reactions of Hg(2+) in foliage. This study demonstrates the diagnostic stable Hg isotopic composition characteristics for separating atmospheric Hg of different source origins in China and provides the isotopic fractionation clues for the study of Hg bioaccumulation.Entities:
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Year: 2016 PMID: 27485289 DOI: 10.1021/acs.est.6b01782
Source DB: PubMed Journal: Environ Sci Technol ISSN: 0013-936X Impact factor: 9.028