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Re-Os geochronology of organic rich sediments: an evaluation of organic matter analysis methods

机译:富含有机质沉积物的Re-Os年代学:有机质分析方法的评估

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Rhenium and osmium in organic-rich sedimentary rocks are dominantly hydrogenous, but any nonhydrogenous component will influence the accuracy and precision of the Re-Os date obtained. To minimize the influence of any nonhydrogenous Re and Os, we evaluate analysis of isolated organic matter from the whole rock, together with whole rock analysis using a CrO3-H2SO4 digestion medium instead of inverse aqua regia, for a black shale unit of the Exshaw Formation, Canada. This unit previously returned a whole rock Re-Os date of 358 +/- 10 Ma (Model 3) [Geochim. Cosmochim. Acta (2002)] using inverse aqua regia dissolution. Organic matter isolated from the whole rock matrix using the HF-BF3 technique [Org. Geochem. 20 (1993) 249] yields scattered data and a Re-Os date of 449 220 Ma (Model 3, MSWD = 616). The organic matter analyses show similar Os-187/Os-188 values, but significantly lower Re-187/Os-188 values in comparison to the whole rock analyses. We show that the Re-Os systematics of organic matter are altered during chemical isolation, and as such we suggest that the HF-BF3 method should not be used for Re-Os analysis of organic matter. Whole rock Re-Os analysis using a CrO3-H2SO4 digestion medium yields significantly better regression analysis compared with the inverse aqua regia method, and the Re-Os data identify two distinct initial Os-187/Os-188 values for the sample set. Separate regressions of these data yield precise dates [366.1 +/- 9.6, MSVvD = 2.2 and 363.4 +/- 5.6 Ma, MSWD = 1.6 (Model 3)], which are indistinguishable from the age constraints for this formation (363.4 +/- 0.4 Ma, U-Pb monazite). Comparison of the Re-Os dates obtained from aqua regia and CrO3-H2SO4 methods suggests that the former may contain nonhydrogenous Re and Os, whereas the CrO3-H2SO4 method dominantly liberates hydrogenous Re-Os from organic matter, allowing for better stratigraphic age determinations and evaluation of the Os isotope composition of seawater. (C) 2003 Elsevier B.V. All rights reserved. [References: 49]
机译:富含有机物的沉积岩中的and和ly主要为氢,但是任何非氢成分都会影响所获得的Re-Os数据的准确性和精度。为了最大程度地减少任何非氢的Re和Os的影响,我们对Exshaw组的黑色页岩单元评估了从整个岩石中分离出的有机物的分析,以及使用CrO3-H2SO4消化介质而不是反向王水进行的整个岩石分析。 ,加拿大。该装置之前返回的整个岩石Re-Os日期为358 +/- 10 Ma(模型3)[Geochim。宇宙猫Acta(2002)]使用反向王水溶解。使用HF-BF3技术从整个岩石基质中分离出有机物[Org。地球化学。 20(1993)249]产生分散的数据,Re-Os日期为449220 Ma(模型3,MSWD = 616)。有机物分析显示出相似的Os-187 / Os-188值,但与整个岩石分析相比,Re-187 / Os-188值明显较低。我们表明,化学分离过程中有机物的Re-Os系统发生了变化,因此,我们建议不应将HF-BF3方法用于有机物的Re-Os分析。与反向王水法相比,使用CrO3-H2SO4消化介质对整个岩石进行Re-Os分析可获得更好的回归分析,并且Re-Os数据确定了样品组的两个不同的初始Os-187 / Os-188值。这些数据的单独回归得出精确的日期[366.1 +/- 9.6,MSVvD = 2.2和363.4 +/- 5.6 Ma,MSWD = 1.6(模型3)],这与该构造的年龄约束没有区别(363.4 +/- 0.4 Ma,U-Pb独居石)。通过王水法和CrO3-H2SO4法获得的Re-Os日期的比较表明,前者可能含有非氢Re-和Os,而CrO3-H2SO4法则主要从有机质中释放出氢Re-Os,从而可以更好地确定地层年龄和对海水中Os同位素组成的评估(C)2003 Elsevier B.V.保留所有权利。 [参考:49]

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