Historical Records of Mercury Stable Isotopes in Sediments of Tibetan Lakes

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作者
Runsheng Yin
Xinbin Feng
James P. Hurley
David P. Krabbenhoft
Ryan F. Lepak
Shichang Kang
Handong Yang
Xiangdong Li
机构
[1] State Key Laboratory of Environmental Geochemistry,Department of Civil and Environmental Engineering
[2] Institute of Geochemistry,Department of Civil and Environmental Engineering
[3] Chinese Academy of Sciences,undefined
[4] Environmental Chemistry and Technology Program,undefined
[5] University of Wisconsin-Madison,undefined
[6] Madison,undefined
[7] University of Wisconsin-Madison,undefined
[8] Madison,undefined
[9] University of Wisconsin Aquatic Sciences Center,undefined
[10] Madison,undefined
[11] U.S. Geological Survey,undefined
[12] Mercury Research Laboratory,undefined
[13] Middleton,undefined
[14] State Key Laboratory of Cryospheric Sciences,undefined
[15] Cold and Arid Regions Environmental and Engineering Research Institute,undefined
[16] Chinese Academy of Sciences,undefined
[17] CAS Center for Excellence in Tibetan Plateau Earth Sciences,undefined
[18] Chinese Academy of Sciences,undefined
[19] Environmental Change Research Centre,undefined
[20] University College London,undefined
[21] Pearson Building,undefined
[22] Gower Street,undefined
[23] The Hong Kong Polytechnic University,undefined
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摘要
The Tibetan Plateau (TP), known as the “Third Pole”, is a critical zone for atmospheric mercury (Hg) deposition. Increasing anthropogenic activities in the globe leads to environmental changes, which may affect the loading, transport and deposition of Hg in the environment. However, the deposition history and geochemical cycling of Hg in the TP is still uncertain. Our records of Hg and Hg isotopes in sediment profiles of the two largest lakes in the TP, Lake Qinghai and Nam Co, show increased Hg influx since last century, with the maximum Hg influx enrichment ratios of 5.4 and 3.5 in Lake Qinghai and Nam Co, respectively. Shifts in negative δ 202Hg in Lake Qinghai (−4.55 to −3.15‰) and Nam Co (−5.04 to −2.16‰) indicate increased atmospheric Hg deposition through rainfall, vegetation and runoff of soils. Mass independent fractionation of both even-Hg (∆ 200Hg: +0.05 to +0.10‰) and odd-Hg (∆ 199Hg: +0.12 to +0.31‰) isotopes were observed. Positive Δ 200Hg suggest high proportion of precipitation-derived Hg in the TP, whereas the positive Δ 199Hg results from Hg(II) photo-reduction. Both lakes show increasing Δ 199Hg since the 1900 s and we conclude that with the decrease of ice duration, Hg(II) photo-reduction may have been accelerated in these TP lakes.
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