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Source and origin of active and fossil thermal spring systems,northern Upper Rhine Graben,Germany
Authors:Anselm Loges  Thomas Wagner  Thomas Kirnbauer  Susanne Göb  Michael Bau  Zsolt Berner  Gregor Markl
Institution:1. Fachbereich Geowissenschaften, Universität Tübingen, D-72074 Tübingen, Germany;2. Institute of Geochemistry and Petrology, ETH Zurich, CH-8092 Zürich, Switzerland;3. Technische Fachhochschule Georg Agricola, D-44787 Bochum, Germany;4. Earth & Space Sciences Program, Jacobs University, D-28759 Bremen, Germany;5. Institute of Mineralogy and Geochemistry, Karlsruhe Institute of Technology, D-76131 Karlsruhe, Germany
Abstract:Thermal water samples and related young and fossil mineralization from a geothermal system at the northern margin of the Upper Rhine Graben have been investigated by combining hydrochemistry with stable and Sr isotope geochemistry. Actively discharging thermal springs and mineralization are present in a structural zone that extends over at least 60 km along strike, with two of the main centers of hydrothermal activity being Wiesbaden and Bad Nauheim. This setting provides the rare opportunity to link the chemistry and isotopic signatures of modern thermal waters directly with fossil mineralization dating back to at least 500–800 ka. The fossil thermal spring mineralization can be classified into two major types: barite-(pyrite) fracture filling associated with laterally-extensive silicification; and barite, goethite and silica impregnation mineralization in Tertiary sediments. Additionally, carbonatic sinters occur around active springs. Strontium isotope and trace element data suggest that mixing of a hot (>100 °C), deep-sourced thermal water with cooler groundwater from shallow aquifers is responsible for present-day thermal spring discharge and fossil mineralization. The correlation between both Sr and S isotope ratios and the elevation of the barite mineralization relative to the present-day water table in Wiesbaden is explained by mixing of deep-sourced thermal water having high 87Sr/86Sr and low δ34S with shallow groundwater of lower 87Sr/86Sr and higher δ34S. The Sr isotope data demonstrate that the hot thermal waters originate from an aquifer in the Variscan crystalline basement at depths of 3–5 km. The S isotope data show that impregnation-type mineralization is strongly influenced by mixing with SO4 that has high δ34S values. The fracture style mineralization formed by cooling of the thermal waters, whereas impregnation-type mineralization precipitated by mixing with SO4-rich groundwater percolating through the sediments.
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