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Controls on Sr isotopic evolution in lacustrine systems: Eocene green river formation,Wyoming

机译:湖泊系统中Sr同位素演化的控制:怀俄明州始新世绿河形成

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Strontium isotopes from lacustrine carbonates record detailed weathering histories of exposed bedrocks, and thus are potentially useful for understanding interactions between tectonics and climate that may be driven by local or regional factors in basin-scale hydrologic systems. We combine extensive ~(87)Sr/~(86)Sr and δ~(18)O datasets fromthe Green River Formation in order to identify environmental factors driving the evolution of Sr concentration and isotopic composition in lacustrine systems through the use of Srmass balancemodeling. Twomodels are developed. The first tests the effect of drainage capture that drove a constant-volume lake frombalance-filled to overfilled conditions, and is applied to the Laney Member of the Green River Formation. The second model focuses on lacustrine evolution in response to changing the concentration, composition, and mass of water influx in a variable-size Sr reservoir (lake). This model is applied to the Wilkins Peak Member of the Green River Formation.~(87)Sr/~(86)Sr ratios are correlated with δ~(18)O values only during the Laney Member, when both are readily explained by a common forcing mechanism (drainage capture). Modeling of Sr isotope compositions and concentrations indicates a short residence time for Sr (~10~3-10~4 years or less) in both balance-overfilled and underfilled phases of the Green River Formation lacustrine system. This in turn suggests that paleo-lacustrine sediments in most lakes can preserve Sr isotope records with high-resolution (~10~2 years) timescales. Rates of Sr sequestration in carbonate are shown to have a strong influence on lacustrine Sr concentration, and high Sr concentrations of lacustrine carbonate consistent with high salinity are observed in the underfilled Wilkins Peak Member and the balance-filled Tipton and lower Laney Members. In the Laney Member, ~(87)Sr/~(86)Sr mass-balance modeling results provide additional support for previous interpretations that the introduction of a large drainage system produced an isotopic shift across the lower LaClede/upper LaClede boundary. Major drainage reorganization is not required to drive high variability in ~(87)Sr/~(86)Sr ratios, however. Modeling shows that variability in ~(87)Sr/~(86)Sr ratios of ~0.004 observed in the Wilkins Peak Member can be explained by change in the characteristics of intrabasinal water sources during highstand vs. lowstand conditions.
机译:来自湖相碳酸盐的锶同位素记录了裸露基岩的详细风化历史,因此对于了解构造学与气候之间的相互作用(可能由流域规模的水文系统中的局部或区域因素驱动)具有潜在的帮助。我们结合了来自绿河组的大量〜(87)Sr /〜(86)Sr和δ〜(18)O数据集,以通过Srmass平衡模型确定驱动湖泊系统中Sr浓度和同位素组成演变的环境因素。 。开发了两种模型。第一个测试排水捕获的作用,将恒定体积的湖泊从平衡填充状态变为过度填充状态,并将其应用于绿河组的莱尼河段。第二个模型着眼于湖泊的变化,以响应变大小的Sr储层(湖泊)中涌入水的浓度,组成和质量的变化。该模型适用于绿河组的威尔金斯峰成员。〜(87)Sr /〜(86)Sr比值仅在Laney成员期间与δ〜(18)O值相关,而这两者很容易用a解释。常见的强迫机制(排水捕获)。 Sr同位素组成和浓度的模型表明,Sr在绿河组湖相系统的平衡充填阶段和充填不足阶段均停留时间短(〜10〜3-10〜4年或更短)。这反过来表明,大多数湖泊中的古湖沉积物可以高分辨率(〜10〜2年)的时间尺度保存Sr同位素记录。碳酸盐中的Sr固存速率显示出对湖泊中Sr浓度的强烈影响,并且在未充分填充的Wilkins Peak成员以及平衡填充的Tipton和较低的Laney成员中观察到高Sr浓度的湖泊碳酸盐与高盐度一致。在Laney成员中,〜(87)Sr /〜(86)Sr质量平衡建模结果为以前的解释提供了额外的支持,即引入大型排水系统会在LaLaedede下部/ LaClede上部边界产生同位素位移。但是,不需要大的排水改组来驱动〜(87)Sr /〜(86)Sr比值的高变异性。建模显示,在威尔金斯峰成员中观察到的〜(87)Sr /〜(86)Sr比值的〜0.004的变异性可以用高水位与低水位条件下基底内水源的特征变化来解释。

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