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Sr isotopes in natural waters: Applications to source characterisation and water-rock interaction in contrasting landscapes

机译:天然水体中的Sr同位素:在对比景观中用于源表征和水-岩相互作用的应用

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Strontium isotopes are now routinely measured in hydrochemical studies to determine sources and mixing relationships. It is often assumed that in contrast to the commonly used stable isotopes of O,H, C and S, 87Sr/86Sr is not fractionated by low temperature processes such as dissolution and precipitation.However, recent modelling and laboratory studies have enhanced our understanding of how Sr isotopes behave in low temperature environments and challenged early assumptions about Sr behaviour. High 8TSr/86Sr may for example be caused by the preferential release of 87Sr from sites previously occupied by 87Rb due to contrasting ionic radii. Furthermore, variations in the weathering rates and mechanisms of different minerals can often make determining the weathering component of environments difficult. Nevertheless, Sr isotopes are useful, when combined with other hydrochemical data, to constrain models of water-rock interaction and mixing as well as geochemical processes such as ion-exchange. This paper presents a summary of recent work by the authors in constraining the sources of waters and weathering processes in surface catchments and aquifers.
机译:现在在水化学研究中对锶同位素进行常规测量,以确定来源和混合关系。通常认为,与常用的O,H,C和S稳定同位素相反,87Sr / 86Sr不会被诸如溶解和沉淀之类的低温过程所分离,但是最近的建模和实验室研究增强了我们对Sr同位素在低温环境中的行为如何,并挑战了有关Sr行为的早期假设。高8TSr / 86Sr可能是例如,由于对比的离子半径,优先从先前被87Rb占据的位点释放了87Sr。此外,不同矿物的风化速率和机理的变化通常会使确定环境的风化成分变得困难。然而,当与其他水化学数据结合使用时,Sr同位素对于约束水-岩相互作用和混合以及地球化学过程(例如离子交换)的模型是有用的。本文概述了作者近期在限制集水区和含水层中的水源和风化过程方面所做的最新工作。

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