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Johnson, J. S., Baker, L. A., & Fox, P. (1999). Geochemical transformations during artificial groundwater recharge: soil–water interactions of inorganic constituents. Water research, 33(1), 196–206.
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Vengosh, A., Spivack, A. J., Artzi, Y., & Ayalon, A. (1999). Geochemical and boron, strontium, and oxygen isotopic constraints on the origin of the salinity in groundwater from the Mediterranean coast of Israel. Water Resources Research, 35(6), 1877–1894.
Abstract: In order to identify the origin of the salinity and formation of saline plumes in the central part of the Mediterranean coastal aquifer of Israel, we determined the elemental and boron, strontium, and oxygen isotopic compositions of fresh and brackish groundwater (C1 up to 1500 mg/L). We distinguish between two key anthropogenic sources: (1) sewage effluents used for irrigation with high Na/C1, SO4/C1, and B/C1 ratios and low Br/C1 ratios relative to seawater ratios, low ;5•B values (0-10%o) and high ;5•80 values (>-4%0); and (2) imported water from the Sea of Galilee that is artificially
recharged tothe aquifer with high Br/C1 (3 x 10 -3) and ;5•80 values (-1%o) and a low 87Sr/86Sr ratio of 0.70753. The brackish groundwater from the saline plumes have relatively low Na/C1 ratios (0.5-0.8) and high Ca/Mg, Mg/C1, and Ca/(SO 4 q- HCO3) (> l) ratios relative to seawater ratios; marine SO4/C1 and Br/C1 ratios;5•B values of 24.8-49.9%0; 18 87 86 ;50 of -2.95%0 to -4.73%0; and Sr/ Sr ratios of 0.708275-0.708532. The composition of most of the investigated groundwater from the saline plumes differs from those of the 87 86 anthropogenic sources, imported water, fresh uncontaminated groundwater (Sr/ Sr of 0.70866, ;5•B of 20-30%o), and saline water from the adjacent Eocene aquitard. Only in ß 18 areas of artificial recharge does local groundwater have high Br/C1 and ;50 values that are typical to the Sea of Galilee. The linear relationships between chloride and most of the ions, including Band Sr, the relatively high ;5•B (>30%0) and low ;5•80 (<-4%0) values, and the chemical signature of the saline plumes (e.g., marine Br/C1 and SO4/C1 ratios), suggest that (1) mixing processes control the chemical composition of the brackish water within the aquifer, and (2) the saline postulated end-member has a chemical composition that resembles modified seawater with a marine and higher ;5•B values, and a 87Sr/86Sr ratio of <0.7083. We propose that most of the salinization phenomena and the formation of saline plumes in the inner parts of the coastal aquifer are derived from upconing of underlying natural saline water bodies and enhanced by overexploitation and draw-down of the overlying fresh groundwater.
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Glavas, S., & Moschonas, N. (2002). Origin of observed acidic–alkaline rains in a wet-only precipitation study in a Mediterranean coastal site, Patras, Greece. Atmospheric Environment, 36(19), 3089–3099.
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Schmittner, K. - E., & Giresse, P. (1999). The impact of atmospheric sodium on erodibility of clay in a coastal Mediterranean region. Environmental Geology, 37(3), 195–206.
Abstract: Heavy rainfalls, between 25 and 100 mm·h–1, were simulated on Pliocene/Quaternary sediments. To reproduce the heterogeneity of natural environments, 231 small plots of various sizes (between 2.5 and 3.5 m2; mean: about 3 m2) were used. The duration of all simulations was 1 h. We used water that had been collected during natural rainfall. The concentration of clay particles in the sheet wash depended upon the concentration of dissolved sodium in the wash (for about 42%) and of the sheet wash quantity (for about 37%). Under natural water conditions colloidal matter, like clay minerals, is charged negatively and therefore is destabilized by metal cations such as in the case of Na+. Results suggest that relatively higher concentrations of montmorrillonite were related to higher concentrations of sodium as opposed to illite and kaolinite. Microflakes of up to 25 μ were observed to vary between face-to-edge and face-to-face modes (competition between protons and other cations). The concentration of dissolved sodium (Na+) in the runoff water depends on water and sodium balances such as atmospheric input, infiltration, evaporation and surface water runoff. The reduction of vegetation cover increases the amount of salt and amorphous matter in/on the topsoil between heavy rainfall generations. The best predictor to explain montmorillonite, illite and kaolinite in % of mineral clay-sized matter in the surface water runoff (sheet wash) is the percentage of each clay mineral in the topsoil. As opposed to illite and kaolinite, more sheet wash indicate for montmorillonite relatively higher concentrations in the wash. The results of model simulations were confirmed on different field plots of about 1 ha and small catchments during natural heavy rainfall events. Models can also be used to understand and to better simulate sheet, rill and gully erosion, micropedimentation; and pedimentation.
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Khaska, M., Salle], C. [L. G. L., Lancelot, J., team, A. S. T. E. R., Mohamad, A., Verdoux, P., et al. (2013). Origin of groundwater salinity (current seawater vs. saline deep water) in a coastal karst aquifer based on Sr and Cl isotopes. Case study of the La Clape massif (southern France). Applied Geochemistry, 37, 212–227.
Abstract: In this study a typical coastal karst aquifer, developed in lower Cretaceous limestones, on the western Mediterranean seashore (La Clape massif, southern France) was investigated. A combination of geochemical and isotopic approaches was used to investigate the origin of salinity in the aquifer. Water samples were collected between 2009 and 2011. Three groundwater groups (A, B and C) were identified based on the hydrogeological setting and on the Cl− concentrations. Average and maximum Cl− concentrations in the recharge waters were calculated (ClRef. and ClRef.Max) to be 0.51 and 2.85mmol/L, respectively). Group A includes spring waters with Cl− concentrations that are within the same order of magnitude as the ClRef concentration. Group B includes groundwater with Cl− concentrations that range between the ClRef and ClRef.Max concentrations. Group C includes brackish groundwater with Cl− concentrations that are significantly greater than the ClRef.Max concentration. Overall, the chemistry of the La Clape groundwater evolves from dominantly Ca–HCO3 to NaCl type. On binary diagrams of the major ions vs. Cl, most of the La Clape waters plot along mixing lines. The mixing end-members include spring waters and a saline component (current seawater or fossil saline water). Based on the Br/Clmolar ratio, the hypothesis of halite dissolution from Triassic evaporites is rejected to explain the origin of salinity in the brackish groundwater. Groundwaters display 87Sr/86Sr ratios intermediate between those of the limestone aquifer matrix and current Mediterranean seawater. On a Sr mixing diagram, most of the La Clape waters plot on a mixing line. The end-members include the La Clape spring waters and saline waters, which are similar to the deep geothermal waters that were identified at the nearby Balaruc site. The 36Cl/Cl ratios of a few groundwater samples from group C are in agreement with the mixing hypothesis of local recharge water with deep saline water at secular equilibrium within a carbonate matrix. Finally, PHREEQC modelling was run based on calcite dissolution in an open system prior to mixing with the Balaruc type saline waters. Modelled data are consistent with the observed data that were obtained from the group C groundwater. Based on several tracers (i.e. concentrations and isotopic compositions of Cl and Sr), calculated ratios of deep saline water in the mixture are coherent and range from 3% to 16% and 0% to 3% for groundwater of groups C and B, respectively. With regard to the La Clape karst aquifer, the extension of a lithospheric fault in the study area may favour the rise of deep saline water. Such rises occur at the nearby geothermal Balaruc site along another lithospheric fault. At the regional scale, several coastal karst aquifers are located along the Gulf of Lion and occur in Mezosoic limestones of similar ages. The 87Sr/86Sr ratios of these aquifers tend toward values of 0.708557, which suggests a general mixing process of shallow karst waters with deep saline fossil waters. The occurrence of these fossil saline waters may be related to the introduction of seawater during and after the Flandrian transgression, when the highly karstified massifs invaded by seawater, formed islands and peninsulas along the Mediterranean coast.
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