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Aircraft Measurements of Total Mercury and Monomethyl Mercury in Summertime Marine Stratus Cloudwater from Coastal California, USA

机译:美国沿海加州夏季海洋层云水中的总汞和一甲基汞的飞机测量

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摘要

Water samples from marine stratus clouds were collected during 16 aircraft flights above the Pacific Ocean near the Central California coast during the summer of 2016. These samples were analyzed for total mercury (THg), monomethyl mercury (MMHg), and 32 other chemical species in addition to aerosol physical parameters. The mean concentrations of THg and MMHg in the cloudwater samples were 9.2 ± 6.0 ng L~(–1) (2.3–33.8 ng L~(–1)) ( N = 97) and 0.87 ± 0.66 ng L~(–1) (0.17–2.9 ng L~(–1)) ( N = 22), respectively. This corresponds to 9.5% (3–21%) MMHg as a fraction of THg. Low and high nonsea salt calcium ion (nss-Ca~(2+)) concentrations in cloudwater were used to classify flights as “marine” and “continental”, respectively. Mean [MMHg]_(marine) was significantly higher ( p < 0.05) than [MMHg]_(continental) consistent with an ocean source of dimethyl Hg (DMHg) to the atmosphere. Mean THg in cloudwater was not significantly different between the two categories, indicating multiple emissions sources. Mean [THg]_(continental) was correlated with pH, CO, NO_(3)~(–), NH_(4)~(+), and other trace metals, whereas [THg]_(marine) was correlated with MMHg and Na~(+). THg concentrations were negatively correlated with altitude, consistent with ocean and land emissions, coupled with removal at the cloud-top due to drizzle formation.
机译:2016年夏季,在加利福尼亚中部海岸附近的太平洋上空进行的16架飞机飞行中,从海洋地层云中收集了水样。分析了这些水样中的总汞(THg),一甲基汞(MMHg)和其他32种化学物质。除了气溶胶的物理参数。浊水样品中THg和MMHg的平均浓度为9.2±6.0 ng L〜(–1)(2.3–33.8 ng L〜(–1))(N = 97)和0.87±0.66 ng L〜(–1) (0.17–2.9 ng L〜(–1))(N = 22)。这相当于9.5%(3–21%)MMHg,仅占THg的一部分。在云水中低和高的非海盐钙离子(nss-Ca〜(2+))浓度分别将飞行分类为“海洋”和“大陆”。平均[MMHg] _(海洋)明显高于[MMHg] _(大陆)(与大气中的二甲基汞(DMHg)海洋来源一致)(p <0.05)。两种水中的云水中THg的平均值无显着差异,表明存在多种排放源。 [THg] _(大陆)与pH,CO,NO_(3)〜(–),NH_(4)〜(+)和其他痕量金属相关,而[THg] _(海洋)与MMHg相关。和Na〜(+)。 THg浓度与海拔高度呈负相关,与海洋和陆地的排放量一致,并由于毛毛雨形成而在云顶去除。

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  • 来源
    《Environmental Science & Technology》 |2018年第5期|2527-2537|共11页
  • 作者单位

    Department of Microbiology and Environmental Toxicology, University of California at Santa Cruz, Santa Cruz, California 95064, United States;

    Department of Chemical and Environmental Engineering, University of Arizona, Tucson, Arizona 85721, United States,Department of Hydrology and Atmospheric Sciences, University of Arizona, Tucson, Arizona 85721, United States;

    Moss Landing Marine Laboratories, Moss Landing, California 95039, United States;

    Moss Landing Marine Laboratories, Moss Landing, California 95039, United States;

    NASA Langley Research Center, Hampton, Virginia 23666, United States;

    Department of Chemical and Environmental Engineering, University of Arizona, Tucson, Arizona 85721, United States;

    Department of Chemical and Environmental Engineering, University of Arizona, Tucson, Arizona 85721, United States;

    Department of Chemical and Environmental Engineering, University of Arizona, Tucson, Arizona 85721, United States;

    Naval Postgraduate School, Monterey, California 93943, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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