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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Oxyanions in metalliferous sediments: Tracers for paleoseawater metal concentrations?
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Oxyanions in metalliferous sediments: Tracers for paleoseawater metal concentrations?

机译:含金属沉积物中的高氧阴离子:示踪剂,用于检测古水金属浓度吗?

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The concentration of carbon, Fe, Mn, S, P, V, Cr, As, Mo, Cd, U, and Re were determined in sediment core Y-71-7-53P near an active hydrothermal location on the southern East Pacific Rise crest (10 degreesS). The goal was to determine the usefulness of hydrothermal iron oxides as carriers of elemental tracers of seawater concentrations. The sediments are 70% carbonate and about 1.3% detrital material, with the remainder having a hydrothermal origin. Rhenium concentrations are at detrital levels suggesting little anaerobic diagenesis beyond manganese remobilization; however, U, Cd, and Mo concentrations all indicate alteration after deposition. Oxyanion/Fe ratios of P, V, and As in surface sediments are lower than the ratios in plume particles and covary with Fe content downcore. The probable explanation for these variations is variable efficiency of incorporation of these metals during iron oxide formation or early diagenetic processes after deposition. The P/Fe ratio in the core sediment is about half that in the plume particles. Among the oxyanion ratios, only the V/As ratio in the sediments is relatively constant at the present plume particle ratio during the past 60-70 kyr. Changes in sediments older than this could reflect variability in the incorporation efficiency or changes in V/As ratio in seawater. This study demonstrates the difficulties of using hydrothermal sediment element enrichments as tracers of past seawater chemistry changes. In this core it appears that all oxyanion ratios change for reasons other than seawater metal concentration changes, with the possible exception of the V/As ratio. Copyright (C) 2000 Elsevier Science Ltd. [References: 64]
机译:确定了东太平洋南部上升热液活动区附近沉积岩心Y-71-7-53P中碳,铁,锰,硫,磷,钒,铬,砷,钼,镉,铀和Re的浓度波峰(10度)。目的是确定水热氧化铁作为海水中元素示踪剂的载体的有用性。沉积物为70%的碳酸盐和约1.3%的碎屑物质,其余部分为水热成因。浓度处于碎屑水平,表明除锰迁移外几乎没有厌氧成岩作用。但是,U,Cd和Mo的浓度都表明沉积后发生了变化。表层沉积物中P,V和As的氧离子/铁比低于羽状颗粒和鸟笼中的铁,铁含量较低。这些变化的可能解释是在形成氧化铁或沉积后早期成岩过程中这些金属的掺入效率可变。核心沉积物中的P / Fe比约为羽状颗粒的一半。在含氧阴离子比率中,在过去的60-70年间,只有沉积物中的V / As比在当前羽状颗粒比下相对恒定。早于此的沉积物变化可能反映掺入效率的变化或海水中V / As比的变化。这项研究证明了使用热液沉积物元素富集作为过去海水化学变化的示踪剂的困难。在这个核心中,似乎所有的氧阴离子比率都因海水金属浓度变化以外的原因而变化,可能是V / As比率例外。版权所有(C)2000 Elsevier Science Ltd. [参考:64]

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