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Anthropogenic Forcings on the Surficial Osmium Cycle

机译:人为强迫对表面O周期的影响

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摘要

Osmium is among the least abundant elements in the Earth's continental crust Recent anthropogenic Os contamination of the environment from mining and smelting activities, automotive catalytic converter use, and hospital discharges has been documented. Here we present evidence for anthropogenic overprinting of the natural Os cycle using a ca. 7000-year record of atmospheric Os deposition and isotopic composition from an ombrotrophic peat bog in NW Spain, Preanthropogenic Os accumulation in this area is 0.10 ± 0.04 ng m~2 y~(-1). The oldest strata showing human influence correspond to early metal mining and processing on the Iberian Peninsula (ca. 4700-2500 cal. BP). Elevated Os accumulation rates are found thereafter with a local maximum of 1.1 ng M~(-2) y~(-1) during the Roman occupation of the Iberian Peninsula (ca. 1930 cal. BP) and a further increase starting in 1750 AD with Os accumulation reaching 30 ng m~2 y~(-1) in the most recent samples. Osmium isotopic composition (~(187)Os/~(188)Os) indicates that recent elevatedrnOs accumulation results from increased input of unradiogenic Os from industrial and automotive sources as well as from enhanced deposition of radiogenic Os through increased fossil fuel combustion and soil erosion. We posit that the rapid increase in catalyst-equipped vehicles, increased fossil fuel combustion, and changes in land-use make the changes observed in NW Spain globally relevant.
机译:is是地球上地壳中含量最低的元素之一,最近有文献记载,采矿,冶炼活动,汽车催化转化器的使用以及医院排放等人为污染的Os污染环境。在这里,我们提供使用ca的自然Os循环的人为套印证据。西班牙西北部一个非营养型泥炭沼泽的大气Os沉积和同位素组成已有7000年的记录,该地区的人为源性Os积累为0.10±0.04 ng m〜2 y〜(-1)。显示出人类影响力的最古老地层对应于伊比利亚半岛的早期金属开采和加工(约4700-2500 cal。BP)。此后发现升高的Os积累速率,在罗马占领伊比利亚半岛(约1930 BP)期间,最大局部累积量为1.1 ng M〜(-2)y〜(-1),并在公元1750年开始进一步增加在最近的样本中,Os累积达到30 ng m〜2 y〜(-1)。 iso同位素组成(〜(187)Os /〜(188)Os)表明,最近的rnOs积累增加是由于工业和汽车来源的非放射性Os的输入增加,以及由于化石燃料燃烧和土壤侵蚀增加而导致的放射性Os沉积增加。我们认为配备催化剂的车辆的迅速增加,化石燃料燃烧的增加以及土地使用的变化使西班牙西北部的变化具有全球意义。

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  • 来源
    《Environmental Science & Technology》 |2010年第3期|881-887|共7页
  • 作者单位

    Water Environment Technology, Department of Civil and Environmental Engineering, Chalmers University of Technology, 41296 Goeteborg, Sweden;

    Department of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution, Woods Hole, Massachusetts 02543;

    Department of Geology and Geochemistry, Stockholm University, 10691 Stockholm, Sweden;

    Earth Science and Engineering, Imperial College London, SW72AZ London, U.K., Mineralogy, The Natural History Museum, London, SW7 5PD, London U.K.;

    Edafologia y Quimica Agricola, Facultad de Biologia, Universidad de Santiago de Compostela-Catnpus Sur, 15782 Santiago, Spain;

    Department of Geosciences, University of Bremen, 28359 Bremen, Germany;

    Departament de FisicaUniversitat Autbnoma de Barcelona, E-08193 Bellaterra, Spain;

    School of Geosciences, University of Aberdeen, Aberdeen, AB243UF, Scotland, U.K.;

    epartment of Civil and Environmental Engineering, Massachusetts institute of Technology, Cambridge, Massachusetts 02139;

  • 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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  • 正文语种 eng
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  • 入库时间 2022-08-17 14:03:53

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