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Tracing the composition, fluid source and formation conditions of the methane-derived authigenic carbonates in the Gulf of Cadiz with rare earth elements and stable isotopes

机译:利用稀土元素和稳定同位素追踪加的斯湾甲烷衍生的自生碳酸盐的组成,流体源和形成条件

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The mineral composition, stable carbon and oxygen isotopes, and rare earth element (REE) concentrations in methane-derived authigenic carbonates collected from the Gulf of Cadiz were used to trace fluid sources and examine the controlling factors on REE composition during carbonate formation. These authigenic carbonate samples are composed of a detrital fraction (mainly quartz and clay) cemented by authigenic carbonate minerals: aragonite and Mg-calcite, pure Mg-calcite, or dolomite and Mg-calcite. The delta C-13 values of the whole rock samples vary between -45.8 parts per thousand and -9.7 parts per thousand VPDB and delta O-18 values range from 3.7 parts per thousand to 6.9 parts per thousand VPDB. The delta C-13 values are indicative of a methane-derived source for these carbonates, most likely resulting from thermogenic gas or a mixture of thermogenic and biogenic gas. The total REE content (Sigma REE) of these authigenic carbonate minerals range from 13 to 31 ppm; all but four of the subsamples are lower than a typical marine carbonates (similar to 28 ppm). This suggests that the REE composition of methane-derived authigenic carbonates is controlled primarily by the methane-rich fluids. The results also show that the REE contents in carbonate mineral subsamples containing dolomite and Mg-calcite is higher than those subsamples with aragonite, suggesting that the authigenic mineral composition and the formation environment are important factors. The shale-normalized REE patterns of the seep carbonates show no or slightly positive Ce anomalies, suggesting that the formation of these seep carbonates occurred under anoxic conditions and associated with rapid fluid seepage. The correlation results of Ce/Ce* and LaN/SmN, Ce/Ce* and Dy-N/Sm-N, and Ce/Ce* and mREE suggest that the REE characteristics of most seep carbonate samples preserve the original redox conditions of their formation. Late diagenesis or post-oxidation of the samples by their exhumation from the sediments into seawater has little effect on REEs. Therefore, it can be assumed these methane-derived authigenic carbonates represent primary carbonate phases; they have not undergone significant diagenesis and their geochemical and isotopic signatures mainly reflect their formation processes. (C) 2015 Elsevier Ltd. All rights reserved.
机译:从加的斯湾收集的甲烷来源的自生碳酸盐中的矿物成分,稳定的碳和氧同位素以及稀土元素(REE)浓度用于追踪流体源并检查碳酸盐形成过程中REE组成的控制因素。这些自生碳酸盐样品由碎屑级分(主要是石英和粘土)组成,这些碎屑由自生碳酸盐矿物:文石和Mg方解石,纯Mg方解石或白云石和Mg方解石胶结而成。整个岩石样品的C-13增量值在VPDB的-45.8千分之至-9.7千分之间,而O-18的增量C-18值在VPDB的千分之3.7至6.9千分之间。 δC-13值表示这些碳酸盐的甲烷来源,最有可能是由热源气体或热源气体和生物源气体的混合物引起的。这些自生碳酸盐矿物的总REE含量(Sigma REE)范围为13至31 ppm。除四个子样本外,所有样本均低于典型的海洋碳酸盐(约28 ppm)。这表明源自甲烷的自生碳酸盐的REE组成主要受富含甲烷的流体控制。结果还表明,含白云石和镁方解石的碳酸盐矿物子样品中的稀土元素含量高于含文石的碳酸盐矿物子样品中的稀土元素含量,表明自生矿物成分和形成环境是重要因素。渗碳碳酸盐的页岩归一化REE模式显示没有Ce异常或略为正Ce异常,表明这些渗碳碳酸盐的形成发生在缺氧条件下,并且与快速渗漏有关。 Ce / Ce *和LaN / SmN,Ce / Ce *和Dy-N / Sm-N以及Ce / Ce *和mREE的相关结果表明,大多数渗透碳酸盐样品的REE特征保留了其原始氧化还原条件。编队。样品从沉积物中渗出到海水中的后期成岩作用或后氧化作用对REE的影响很小。因此,可以假设这些甲烷衍生的自生碳酸盐代表初级碳酸盐相。它们没有经历明显的成岩作用,其地球化学和同位素特征主要反映了它们的形成过程。 (C)2015 Elsevier Ltd.保留所有权利。

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