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Molybdenum isotope fractionation in pelagic euxinia: Evidence from the modern Black and Baltic Seas

机译:中上游游憩性中的钼同位素分馏:来自现代黑海和波罗的海的证据

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Here we present stable isotope data for vertical profiles of dissolved molybdenum of the modern euxinic water columns of the Black Sea and two deeps of the Baltic Sea. Dissolved molybdenum in all water samples is depleted in salinity-normalized concentration and enriched in the heavy isotope (δ~(98)Mo values up to +2.9‰) compared to previously published isotope data of sedimentary molybdenum from the same range of water depths. Furthermore, δ~(98)Mo values of all water samples from the Black Sea and anoxic deeps of the Baltic Sea are heavier than open ocean water.The observed isotope fractionation between sediments and the anoxic water column of the Black Sea are in line with the model of thiomolybdates that scavenge to particles under reducing conditions. An extrapolation to a theoretical pure MoS_4~(2-) solution indicates a fractionation constant between MoS_4~(2-) and authigenic solid Mo of 0.5±0.3‰. Measured waters with all thiomolybdates coexisting in various proportions show larger but non-linear fractionation. The best explanation for our field observations is Mo scavenging by the thiomolybdates, dominantly - but not exclusively - present in the form of MoS_4~(2-).The Mo isotopic compositions of samples from the sediments and anoxic water column of the Baltic Sea are in overall agreement with those of the Black Sea at intermediate depth and corresponding sulphide concentrations. The more dynamic changes of redox conditions in the Baltic deeps complicate the Black Sea-derived relationship between thiomolybdates and Mo isotopic composition. In particular, the occasional flushing/mixing, of the deep waters, affects the corresponding water column and sedimentary data δ~(98)Mo values of the upper oxic waters of both basins are higher than predicted by mixing models based on salinity variations. The results can be explained by non-conservative behaviour of Mo under suboxic to anoxic conditions in the shallow bottom parts of the basin, most pronounced on the NW shelf of the Black Sea.
机译:在这里,我们为黑海和波罗的海的两个深部的富氧水柱中的溶解钼的垂直剖面提供了稳定的同位素数据。与先前公布的相同水深范围内沉积钼的同位素数据相比,所有水中样品中的溶解钼均以盐分归一化浓度消耗,并且富含重同位素(δ〜(98)Mo值最高为+ 2.9‰)。此外,黑海和波罗的海缺氧深度的所有水样的δ〜(98)Mo值均比公海重,观测到的沉积物与黑海缺氧水柱之间的同位素分馏与在还原条件下清除为颗粒的硫代钼酸盐模型。外推到理论纯MoS_4〜(2-)溶液表明MoS_4〜(2-)与自生固体Mo之间的分馏常数为0.5±0.3‰。以各种比例共存的所有硫代钼酸盐的测得水显示较大但非线性的分馏。对我们的现场观测的最好解释是通过硫代钼酸盐进行的Mo清除,主要但非排他地以MoS_4〜(2-)的形式存在。波罗的海沉积物和缺氧水柱中样品的Mo同位素组成为与黑海的中等深度和相应的硫化物浓度总体上一致。波罗的海深处氧化还原条件的更动态变化使硫代钼酸盐与Mo同位素组成之间的黑海派生关系复杂化。特别是,偶尔的深水冲刷/混合会影响相应的水柱,两个盆地上层含氧水的沉积数据δ〜(98)Mo值均高于基于盐度变化的混合模型所预测的值。该结果可以通过在浅海盆地底部低氧至缺氧条件下Mo的非保守行为来解释,该现象在黑海的西北海段最为明显。

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