Ab'/> Iron geochemistry and organic carbon preservation by iron (oxyhydr)oxides in surface sediments of the East China Sea and the south Yellow Sea
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Iron geochemistry and organic carbon preservation by iron (oxyhydr)oxides in surface sediments of the East China Sea and the south Yellow Sea

机译:铁(Oxyhydr)氧化物在东海和南黄海地表沉积物中铁(氧水)氧化物的铁地球化学和有机碳保存

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AbstractIn marine sediments factors that influence iron (Fe) geochemistry and its interactions with other elements are diverse and remain poorly understood. Here we comparatively study Fe speciation and reactive Fe-bound organic carbon (Fe-OC) in surface sediments of the East China Sea (ECS) and the south Yellow Sea (SYS). The objectives are to better understand the potential impacts of geochemically distinct sediment sources and depositional/diagenetic settings on Fe geochemistry and OC preservation by Fe (hydr)oxides in sediments of the two extensive shelf seas around the world. Contents of carbonate- and acid-volatile-sulfide (AVS)-associated Fe(II) (FeAVS+carb) and magnetite (Femag) in the ECS sediments are about 5 and 9 times higher, respectively, than in the SYS. This could be ascribed to the ferruginous conditions of the ECS sediments that favor the formation/accumulation of Fecarband Femag, a unique feature of marine unsteady depositional regimes. Much lower total Fe(II) contents in the SYS than in the ECS suggest that lower availability of highly reactive Fe (FeHR) and/or weak Fe reduction is a factor limiting Fe(II) formation and accumulation in the SYS sediments. The ratio of FeHRto total Fe is, on average, markedly higher (2.4 times) in the ECS sediments than in the SYS, which may be a combined result of several factors relevant to different sediment sources and depositional/diagenetic settings. In comparison with many other marine sediments, the percent fractions (f
机译:<![cdata [ 抽象 在海洋沉积物中影响铁(Fe)地球化学的因素,其与其他元素的相互作用是多样的,但仍然很差。 。在这里,我们在东海(ECS)和南黄海(SYS)的表面沉积物中进行了比较研究了Fe形态和活性炭有机碳(Fe-OC)。目的是更好地了解地球化学不同的沉积物来源和沉积/岩性环境对世界各地两家广泛货物海洋沉积物中Fe(氢化)氧化物的Fe Geochemisty和OC保存的潜在影响。碳酸酯和酸 - 挥发性 - 硫化物(AVS) - 分配Fe(II)(Fe AVS + Carb )和磁铁矿(Fe Mag ”分别比SYS分别为5至9倍。这可以归因于ECS沉积物的铁格鲁氏状况,有利于FE CARB 和FE MAG ,海洋不稳定沉积制度的独特特征。 SYS中的总Fe(II)含量远低于ECS,表明高反应性Fe的可用性降低(Fe HR )和/或弱FE减少是限制在SYS沉积物中的Fe(II)形成和积累。 FE HR 对总Fe的比率在ECS沉积物中平均明显高(2.4次),而不是SYS,这可能是一个组合结果与不同沉积物来源和沉积/成岩设施相关的几个因素。与许多其他海洋沉积物相比,百分数百分点( f

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