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Sr and Mg isotope geochemistry of the basal Ediacaran cap limestone sequence of Mongolia: Implications for carbonate diagenesis, mixing of glacial meltwaters, and seawater chemistry in the aftermath of Snowball Earth

机译:蒙古基底埃德拉山帽石灰石序列的Sr和Mg同位素地球化学:对碳酸盐融化器的影响,冰球地球后冰川融化器的混合和海水化学

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The seawater chemistry and oceanographic information associated with Snowball Earth are commonly inferred from the geochemistry of cap carbonates deposited on continental margins during and after deglaciation. However, interpretation of such records can be complicated by carbonate diagenesis and contamination from siliciclastic components. In an attempt to disentangle these effects, we studied the geochemistry of the post-Marinoan cap carbonate sequence from Mongolia using a step-leaching procedure, which revealed that most samples are heterogeneous with respect to multiple geochemical signatures, including trace element concentrations, Sr, Mg, C and O isotopic signatures, raising questions to previous studies applying carbonate bulkrock geochemistry for paleoenvironment reconstructions. Such sample heterogeneity can be explained by contamination from non-carbonate phases and carbonate alteration. After stepped leaching, the least-altered/contaminated geochemical signatures for each sample were identified and the influences of carbonate diagenesis were evaluated. Our data indicate that mixing of glacial meltwater persisted to the maximum flooding surface within the cap carbonate sequence, below which carbonates record significant Mg and Sr isotope fluxuations that are most readily interpreted in the context of the mixing of water masses having distinct isotopic compositions. Only limestones deposited above the maximum flooding surface formed in a well-mixed ocean and exhibit Mg and Sr isotope values that record the integrated effects of Snowball Earth on ocean chemistry. Our study cautions against interpreting the geochemistry of cap carbonates in terms of whole ocean geochemical cycles.
机译:与雪球地球相关的海水化学和海洋学信息常见于岩石碳酸帽的地球化学地球化合物,在陆地边缘沉积在下降之后。然而,对这些记录的解释可以通过碳酸酯成岩作用和来自硅质组分的污染来复杂化。为了脱离这些效果,我们使用阶梯浸出程序研究了蒙古玛诺帽碳酸盐序列的地球化学,这揭示了大多数样品相对于多种地球化学签名是异质的,包括痕量元素浓度,SR, Mg,C和O同位素签名,提高对以前研究的问题,适用于古环境重建的碳酸盐散装地球化学。这些样品异质性可以通过来自非碳酸酯阶段和碳酸酯改变的污染来解释。在阶梯式浸出之后,鉴定了每个样品的最不改变的/污染的地球化学签名,评价碳酸盐酯的影响。我们的数据表明冰川熔融水的混合持续到帽碳酸盖序列内的最大泛洪表面,低于碳酸盐的碳酸盐纳米碳酸盐和Sr同位素丝状物,其在具有不同同位素组合物的水质量的混合的背景下最容易解释。只有沉积在井里混合海洋中形成的最大洪水表面的石灰岩,并且表现出Mg和Sr同位素值,记录雪球地球对海洋化学的综合影响。我们的研究注意到在整个海洋地球化学循环方面解释碳酸帽的地球化学。

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