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Cardenal, J., Benavente, J., & Cruz-Sanjulián, J. J. (1994). Chemical evolution of groundwater in Triassic gypsum-bearing carbonate aquifers (Las Alpujarras, southern Spain). Journal of Hydrology, 161(1), 3–30.
Abstract: A hydrochemical study employing modelling techniques, was carried out using samples taken at 65 points (springs and wells) in Triassic carbonate aquifers (Lújar-Gádor Unit, Alpujárride Complex, Betic Cordillera). These aquifers are made up of limestones and dolomites with some gypsum scattered or interbedded. Though the area is semi-arid, recharge is relatively high because of their mountainous nature. The carbonate rocks contain dense microfissuration; the groundwater flow regime is predominantly diffuse. The karstic forms are in general poorly developed. Two main hydrochemical processes have been identified in these aquifers. One is incongruent dissolution of dolomite that determines the chemical composition of the less mineralised water. The other is dedolomitisation (dolomite dissolution together with calcite precipitation caused by dissolution of gypsum), which becomes predominant when the flow encounters interbedded gypsum. This reaction is also frequently associated with low temperature thermalism, and can play a part in more intense local karstification (cavities, sinkholes, high transmisivity in wells) observed in the sectors of these aquifers where gypsum is more abundant. A reaction path model has been used to simulate the geochemical processes through a hypothetical aquifer (with similar lithology to the Alpujárride carbonate aquifers). Successive stages of evolution through the carbonate sequence, represented by different saturation states with respect to calcite, dolomite gypsum and CO2, have been modelled and then compared with the field data.
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El Yaouti, F., El Mandour, A., Khattach, D., Benavente, J., & Kaufmann, O. (2009). Salinization processes in the unconfined aquifer of Bou-Areg (NE Morocco): A geostatistical, geochemical, and tomographic study. Applied Geochemistry, 24(1), 16–31.
Abstract: Hydrogeological and geochemical data, in conjunction with the results of an electrical imaging tomographic survey, were examined to determine the main factors and mechanisms controlling the groundwater chemistry and salinity of the unconfined aquifer of Bou-Areg, on the Mediterranean coast of NE Morocco. In addition, statistical and geochemical interpretation methods were used to identify the distribution of the salinity. Multivariate statistical analysis (cluster and principal component factors) revealed the main sources of contamination. Groups A, B, and C in the cluster analysis and Factors 1–3 (Factor 1: CE, Cl−, K+, SO42-, and Mg2+; Factor 2: Ca2+, HCO3-, and pH; Factor 3: NO3-) represent the ‘signature’ of seawater intrusion in the coastal zone, the influence of marly-gypsum outcrops in the upstream zone, and anthropogenic sources, respectively. The ionic delta, the ionic ratio, the saturation index, and Stuyfzand’s method were applied to evaluate geochemical processes. The results obtained indicate, on the one hand, the phenomenon of salinization in both the coastal and the upstream zones, and on the other, the dilution of groundwater by recharge. Cation exchange is shown to modify the concentration of ions in groundwater. Locally, with respect to salinization processes in the coastal zone, the results of electrical imaging tomography show that salinity increases both with depth and laterally inland from the coastline, due to seawater intrusion.
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Bobba, A. G. (1993). Mathematical models for saltwater intrusion in coastal aquifers. Water Resources Management, 7(1), 3–37.
Abstract: Flow of freshwater and saltwater intrusion in coastal aquifers has drawn the attention of many investigators. Several laboratory, as well as mathematical models have been developed to study the pattern of flow of groundwater in coastal aquifers. Mathematical models have wider range of application and are the concern of this paper. Due to the complex nature of the problem, each of these mathematical models are based on certain simplifying assumptions and approximations. This paper presents a critical review of various methods of solution which have been proposed. The validity of the results abtained and the limitations of these models are also discussed.
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Kafri, U., Goldman, M., Lyakhovsky, V., Scholl, C., Helwig, S., & Tezkan, B. (2007). The configuration of the fresh–saline groundwater interface within the regional Judea Group carbonate aquifer in northern Israel between the Mediterranean and the Dead Sea base levels as delineated by deep geoelectromagnetic soundings. Journal of Hydrology, 344(1), 123–134.
Abstract: A combined high resolution short offset transient electromagnetic (SHOTEM) and deep sounding, long offset (LOTEM) survey has been carried out along two traverses between the Mediterranean Sea and the Jordan-Dead Sea Rift (DSR). The DSR is located in the study area some 200–250m below sea level. The measurements detected a deep conductor, the top of which exhibited a regular behavior along the both traverses, declining from the Mediterranean to the DSR base level. The geometry of this geoelectric boundary coincides fairly well with the configuration of a supposed fresh/saline groundwater interface as also obtained by both numerical and physical modeling for the known hydrogeological conditions in the study area. Therefore the detected geoelectric boundary is identified with the interface, supporting the hypothesis of current seawater intrusion into the deep regional aquifers between the Mediterranean and the DSR base levels. The intrusion causes the salination of fresh groundwater within the aquifers as well as the salination of the Sea of Galilee.
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Magaritz, M., Nadler, A., Kafri, U., & Arad, A. (1984). Hydrogeochemistry of continental brackish waters in the southern Coastal Plain, Israel. Chemical Geology, 42(1), 159–176.
Abstract: The southern Coastal Plain in Israel incorportates a transitional fringe of the desert in which three different chemical types of groundwater are found: (1) near-surface waters from springs along the Besor River course: (2) shallow- to moderate-depth waters from the slightly westward-dipping Pleistocene coastal aquifer (this aquifer, which consists of sandstone layers of the Kurkar Group, is recharged in the Coastal Plain); and (3) deep waters of the westward-dipping Upper Cretaceous Judea Group carbonates, which are recharged in the mountains in the east. A thick aquiclude of Upper Cretaceous-Tertiary rocks separates the Judea Group aquifer from the overlying coastal aquifer in the southern Coastal Plain. Isotopically light oxygen and depleted deuterium characterize the Judea Group waters, as expected from high-altitude recharge. The isotopic composition of the Coastal Plain waters is variable, but for the most part enriched in 18O and D. Within the southern Coastal Plain aquifer a southern subgroup comprises waters more depleted in heavy isotopes than those of either the northern or eastern subgroups. The Besor waters are isotopically similar to the Judea Group waters, reflecting their origin in the mountain region, and flow through the surficial river gravels and sands. It is suggested that leakage of the Besor waters into the underlying southern Coastal Plain aquifer results in mixing of the two water types. The most prominent chemical feature characterizing the groundwater of the southern Coastal Plain is Na+Cl− \textgreater 1. This Na+Cl− ratio can be maintained only by a continuous input from a non-marine source of Na. The most plausible source of this Na is the dissolution of feldspar derived from the windblown loess deposits which cover the area and/or leaching of trona minerals found in the unsaturated zone, combined with base-exchange processes.
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