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Post-depositional overprinting of chromium in foraminifera

机译:在Foraminifera中染色的后沉积套印

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Present-day ocean deoxygenation has major implications for marine ecosystems and biogeochemical cycling in the oceans. Chromium isotopes are used as a proxy to infer changes in past oceanic redox state. Chromium isotopes in carbonates, including the prime proxy carrier foraminifera, were initially thought to record the seawater composition during crystallisation. However, the uptake of Cr into foraminiferal tests and carbonates is still poorly understood and recent studies question this assumption. We assess whether Cr in foraminiferal calcite is taken up during biomineralisation, has a post-depositional origin or is a combination of the two. Laser Ablation-MC-ICP-MS analyses and NanoSIMS imaging of individual tests were used to characterise the distribution of Cr in both planktic and benthic foraminifera. Foraminifera in sediment core-top samples have up to two orders of magnitude more Cr than sediment trap, plankton net, and culture samples. In cultured specimens, Cr is incorporated in foraminiferal tests at low concentrations (0.04-013 ppm) with a distribution coefficient of similar to 250 +/- 43 (2SE) which is an upper estimate due to substantial loss of dissolved Cr during the experiment. Part of the Cr signal in sedimentary foraminifera may be primary, but this primary signal is likely often overprinted by the uptake of Cr from bottom and pore waters. In sediment samples, there is no significant isotopic offset between individual species and bulk foraminiferal calcite from the same size fraction. The >500 mu m fraction has a heavier isotopic composition than the smaller 250-500 mu m fraction with an offset of -0.3 to -0.5 parts per thousand due to an increase in surface area to volume. We propose that Cr in foraminifera is predominantly post-depositional and records bottom/pore water signals. This is contrary to current interpretations of the foraminiferal Cr isotope proxy as a surface seawater redox proxy. (C) 2019 Elsevier B.V. All rights reserved.
机译:当今海洋脱氧对海洋生态系统和生物地球化学循环有重大影响。铬同位素被用作推断过去海洋氧化还原状态的变化的代理。最初认为在结晶过程中,最初认为碳酸盐中的碳酸铬同位素,包括主要代理载体传染料。然而,CR进入面向敏的试验和碳酸盐仍然明显,最近的研究质疑这种假设。我们评估在生物素化期间是否在生物素化过程中占用Cr,具有沉积后的起源或是两者的组合。激光烧蚀-MC-ICP-MS分析和单个测试的纳米粒子成像用于表征血管和底栖菌的CR的分布。在沉积物中的Foraminifera核心顶部样品比沉积物陷阱,浮游生物网和培养样品更多的Cr更多的数量级。在培养的标本中,Cr以低浓度(0.04-013ppm)掺入多氨基因子试验中,其分布系数类似于250 +/- 43(2se),其是由于在实验期间溶解的CR的大量损失而上升估计。沉积面包素内的一部分CR信号可能是初级的,但是这种主信号可能往往叠印来自底部和孔隙水的Cr的摄取。在沉积物样品中,在相同尺寸的级分中,个体物种和散装花瓶内亚铌之间没有显着同位素偏移。由于表面积增加到体积的增加,>500μm馏分比同位素组合物比较小的250-500μmm馏分较小,其偏移为-0.3至-0.5份。我们提出了Foraminifera中的Cr主要是沉积后和记录底部/孔隙水信号。这与当前对表面海水氧化还原代理的火花素内Cr同位素代理的当前解释相反。 (c)2019 Elsevier B.v.保留所有权利。

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