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从日本海到北极的大气气态元素汞(Hg(0))分布,以及 2018 年秋季俄中联合考察中在东极海域的 Hg(0)逸出通量。

Distribution of atmospheric gaseous elemental mercury (Hg(0)) from the Sea of Japan to the Arctic, and Hg(0) evasion fluxes in the Eastern Arctic Seas: Results from a joint Russian-Chinese cruise in fall 2018.

机构信息

V.I.Il'ichev Pacific Oceanological Institute of Far Eastern Branch of Russian Academy of Sciences, Vladivostok 690041, Russia.

V.I.Il'ichev Pacific Oceanological Institute of Far Eastern Branch of Russian Academy of Sciences, Vladivostok 690041, Russia.

出版信息

Sci Total Environ. 2021 Jan 20;753:142003. doi: 10.1016/j.scitotenv.2020.142003. Epub 2020 Aug 26.

DOI:10.1016/j.scitotenv.2020.142003
PMID:32890877
Abstract

The Eastern Arctic Seas and the north-western Pacific are among the most poorly investigated areas as far as Hg cycling in marine systems is concerned. Continuous measurements of gaseous elemental mercury (Hg(0)) concentrations in the marine boundary layer and Hg(0) evasion fluxes from the sea surface were performed in these regions in fall 2018. Atmospheric Hg(0) concentrations of 1.02-2.50 ng/m were measured (average: 1.45 ± 0.12 ng/m; N = 2518). Values in the Far Eastern Seas of Russia were lower compared to previous observations, presumably reflecting а global trend of decreasing atmospheric Hg(0). Concentration-weighted trajectory analysis highlighted three source regions influencing Hg(0) concentrations in the ambient air during the cruise: 1) the north-eastern China and the Yellow Sea region; 2) the Kuril-Kamchatka region of the Pacific Ocean and the region around the Commander and Aleutian Islands; and 3) the Arctic region. In the Arctic, sea-air Hg(0) evasion fluxes were at the same low levels as those observed earlier in the northern sea areas (0.28-1.35 ng/m/h, average, 0.70 ± 0.26 ng/m/h, N = 29). In the Eastern Arctic Seas, Hg(0) evasion fluxes were significantly dependent on river runoff. In the Arctic Ocean, they were negatively correlated with water temperature and positively correlated with salinity, suggesting a proximity to areas with contiguous ice and higher dissolved Hg(0) concentrations in the surface seawater. These findings are consistent with the hypothesis that the Arctic Ocean is a source of atmospheric Hg(0) during late summer and fall.

摘要

就海洋系统中的汞循环而言,东极海和西北太平洋是研究最少的地区之一。2018 年秋季,在这些地区连续测量了海洋边界层中气态元素汞(Hg(0))浓度和海表面 Hg(0)逸出通量。测量到的大气 Hg(0)浓度为 1.02-2.50 ng/m(平均值:1.45±0.12 ng/m;N=2518)。与先前的观测相比,俄罗斯远东海域的数值较低,这可能反映了大气 Hg(0)全球减少的趋势。浓度加权轨迹分析突出了三个影响巡航期间环境空气中 Hg(0)浓度的源区:1)中国东北和黄海地区;2)太平洋的千岛-堪察加地区以及指挥官群岛和阿留申群岛周围地区;3)北极地区。在北极,海气 Hg(0)逸出通量与早些时候在北部海域观察到的通量处于相同的低水平(0.28-1.35 ng/m/h,平均值 0.70±0.26 ng/m/h,N=29)。在东极海,Hg(0)逸出通量与河川径流量显著相关。在北冰洋,它们与水温呈负相关,与盐度呈正相关,这表明它们与连续冰层和表层海水中溶解 Hg(0)浓度较高的区域接近。这些发现与以下假设一致,即北冰洋是夏末和秋季大气 Hg(0)的来源之一。

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