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Tracking selenium in the Chalk aquifer of northern France: Sr isotope constraints
Institution:1. Institut für Geologie, Mineralogie und Geophysik, Ruhr-Universität Bochum, D-44780 Bochum, Germany;2. Institute of Geosciences, Johannes Gutenberg University, D-55128 Mainz, Germany;1. Physics Division, Argonne National Laboratory, Argonne, IL60439, USA;2. Department of Physics and Enrico Fermi Institute, University of Chicago, Chicago, IL60637, USA;3. School of Nuclear Science and Engineering, University of Science and Technology of China, Hefei, China;4. Climate and Environmental Physics Division, Physics Institute, University of Bern, Bern CH-3012, Switzerland
Abstract:Groundwater at the southern and eastern edges of France’s Paris Basin has a selenium content that at times exceeds the European Framework Directive’s drinking-water limit value of 10 μg/L. To better understand the dynamics of the Chalk groundwater being tapped to supply the city of Lille and the Se origins, we used a combination of geochemical and isotopic tools. Strontium isotopes, coupled with Ca/Sr, Mg/Sr and Se/Sr ratios, were used to identify the main groundwater bodies and their mixings, with the Mg/Sr and Se/Sr ratios constraining a ternary system. Groundwater in the agricultural aquifer-recharge zone represents a first end-member and displays the youngest water ages of the catchment along with the highest Sr isotopic signature (0.70842) and low Se contents. Anaerobic groundwater constitutes a second major end-member affected by water-rock interactions over a long residence time, with the lowest Sr isotopic signature (0.70789) and the lowest Se content, its low SF6 content confirming the contribution of old water. Se-rich groundwater containing up to 30 μg/L of Se represents a third major end-member, with an intermediate Sr isotopic ratio (0.70826), and is mainly constrained by the clayey Se-rich formation overlying the Chalk aquifer. The spatial and temporal Se variability in the groundwater is clearly linked to the presence of this formation identified as Tertiary and also to the hydrological conditions; saturation of the Se-rich clays by oxygenated groundwater enhances Se mobility and also Sr adsorption onto the clays. This multi-tool study including Sr isotopes successfully identified the Se origins in the aquifer and has led to a better understanding of the regional mixing and processes affecting the Chalk groundwater.
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