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Petelet-Giraud, E., Négrel, P., Aunay, B., Ladouche, B., Bailly-Comte, V., Guerrot, C., et al. (2016). Coastal groundwater salinization: Focus on the vertical variability in a multi-layered aquifer through a multi-isotope fingerprinting (Roussillon Basin, France). Science of The Total Environment, 566-567, 398–415.
Abstract: The Roussillon sedimentary Basin (South France) is a complex multi-layered aquifer, close to the Mediterranean Sea facing seasonally increases of water abstraction and salinization issues. We report geochemical and isotopic vertical variability in this aquifer using groundwater sampled with a Westbay System® at two coastal monitoring sites: Barcarès and Canet. The Westbay sampling allows pointing out and explaining the variation of water quality along vertical profiles, both in productive layers and in the less permeable ones where most of the chemical processes are susceptible to take place. The aquifer layers are not equally impacted by salinization, with electrical conductivity ranging from 460 to 43,000μS·cm−1. The δ2H–δ18O signatures show mixing between seawater and freshwater components with long water residence time as evidenced by the lack of contribution from modern water using 3H, 14C and CFCs/SF6. S(SO4) isotopes also evidence seawater contribution but some signatures can be related to oxidation of pyrite and/or organically bounded S. In the upper layers 87Sr/86Sr ratios are close to that of seawater and then increase with depth, reflecting water–rock interaction with argillaceous formations while punctual low values reflect interaction with carbonate. Boron isotopes highlight secondary processes such as adsorption/desorption onto clays in addition to mixings. At the Barcarès site (120m deep), the high salinity in some layers appear to be related neither to present day seawater intrusion, nor to Salses-Leucate lagoonwater intrusion. Groundwater chemical composition thus highlights binary mixing between fresh groundwater and inherited salty water together with cation exchange processes, water–rock interactions and, locally, sedimentary organic matter mineralisation probably enhanced by pyrite oxidation. Finally, combining the results of this study and those of Caballero and Ladouche (2015), we discuss the possible future evolution of this aquifer system under global change, as well as the potential management strategies needed to preserve quantitatively and qualitatively this water resource.
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Carreira, P. M., & Marques, J. M. (2018). Groundwater Salinity and Environmental Change Over the Last 20,000 Years: Isotopic Evidences in the Lower Sado Aquifer Recharge, Portugal. Springer.
Abstract: Impacts of the Water Resources Variability on Cereal Yields in the Region of Souss-Massa Southern MoroccoErstes
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Löhnert, E. P., & Sonntag, C. (1981). Grundwasserversalzungen im Raum Hamburg im Licht neuer Isotopendaten. Zeitschrift der Deutschen Geologischen Gesellschaft, 132, 559–574.
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Nisi, B., Raco B., & Dotsika, E. (2014). Groundwater Contamination Studies by Environmental Isotopes: A review. In E. Jimenez (Ed.), Environment, Energy and Climate Change I: Environmental Chemistry of Pollutants and Wastes. Springer-Verlag Berlin Heidelberg.
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Richter, B. C., & Kreidler, C. W. (1991). Identification of Sources of Groundwater Salinization using Geochemical Techniques. EPA/600/2-91/064, , 259.
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