首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Calculating C-14 mean residence times of inorganic carbon derived from oxidation of organic carbon in groundwater using the principles of Sr-87/Sr-86 and cation ratio mixing
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Calculating C-14 mean residence times of inorganic carbon derived from oxidation of organic carbon in groundwater using the principles of Sr-87/Sr-86 and cation ratio mixing

机译:使用SR-87 / SR-86和阳离子比混合的原理计算地下水中有机碳氧化衍生的无机碳的C-14平均停留时间

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The model radiocarbon age of inorganic carbon (IC) in groundwater is a key parameter for understanding groundwater chemical history and physical parameters such as groundwater residence times and flow rates. Current interpretations are based on the principle that bulk IC derives from multiple sources such as oxidation of organic carbon (OC), carbonate dissolution, and soil zone processes as well as from rainwater. Using this principle, multiple adjustment methods have been developed to calculate rainwater-related recharge ages. Of further interest, however, is the radiocarbon age of oxidised OC. This is a key measurement given that OC oxidation controls the mobility of many important geochemical components such as Fe, As, Mn and U. In this instance, conventional approaches tacitly assume that the majority of IC comes from the oxidation of OC and that other sources have a negligible effect on the bulk age. In reality, however, there are multiple sources of IC which can all effect bulk radiocarbon ages. We present a new approach to calculate the age of IC derived from a specific source. This approach uses strontium isotopes (Sr-87/Sr-86) coupled with elemental ratios to trace and quantify the mixing of different sources of IC. We demonstrate the approach by calculating the model radiocarbon age of IC sourced from the oxidation of OC for a case study of an aquifer in the Cambodian lowlands located adjacent to the Mekong river south of Phnom Penh. The results show that, although bulk IC is younger and more isotopically (delta C-13) depleted than bulk organic carbon (OC), IC derived from oxidation of OC has a similar age and isotopic signature to bulk OC. Furthermore, at our site, the age of the IC formed from the oxidation of organic carbon predates modelled groundwater flow by at least a millennium indicating that in-aquifer oxidation is an important process, something previously questioned at the site. This highlights the utility of the new approach to disentangling the origin of the sources of bulk IC, so critical to the interpretation of its model radiocarbon age and isotopic signature. (C) 2019 Published by Elsevier Ltd.
机译:地下水中无机碳(IC)的模型无碳碳(IC)是理解地下水化学历史和地下水停留时间和流速等物理参数的关键参数。目前的解释基于本原则,该原理来自多种来源,例如有机碳(OC),碳酸盐溶解和土壤区流程以及雨水的氧化。使用该原理,已经开发了多种调整方法来计算雨水相关的充电年龄。然而,进一步的兴趣是氧化oc的含稀碳剂。这是一个关键测量,因为OC氧化控制了许多重要地球化学部件的移动性,例如Fe,AS,Mn和U.在这种情况下,常规方法默许地假设大多数IC来自OC和其他来源的氧化对批量年龄的影响可忽略不计。然而,实际上,有多种IC源,可以所有效果批量无线电金。我们提出了一种计算源自特定来源的IC的年龄的新方法。该方法使用锶同位素(SR-87 / SR-86)与元素比率相结合以追踪和量化不同源IC的混合。我们通过计算邻近金边湄公河南部的柬埔寨低地含水层的OC氧化的IC氧化案例研究来证明该方法。结果表明,虽然散装IC具有比散装有机碳(OC)耗尽的细长且更高的同位素(Delta C-13),但衍生自OC氧化的IC具有类似的年龄和同位素签名,可以散装OC。此外,在我们的网站上,由有机碳氧化形成的IC的年龄通过至少千年表示建模的地下水,表明含水层氧化是一个重要的过程,以前在现场质疑的内容。这突出了新方法解开了批量IC来源的起源的效用,对其模型无碳糖年龄和同位素签名的解释至关重要。 (c)2019年由elestvier有限公司出版

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