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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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Moral, F., Cruz-Sanjulián, J. J., & Olías, M. (2008). Geochemical evolution of groundwater in the carbonate aquifers of Sierra de Segura (Betic Cordillera, southern Spain). Journal of Hydrology, 360(1), 281–296.
Abstract: Sierra de Segura (Betic Cordillera), with a total area of over 3000km2, is the source of the two principal rivers in southern Spain, the Guadalquivir and the Segura. Due to the orographic effect of these mountains, precipitations are considerably more abundant than in nearby lowland areas, where the climate is semi-arid. Sierra de Segura is constituted of Mesozoic and Cenozoic sedimentary rocks, among which there are thick limestone–dolomitic formations which have given rise to extensive outcrops of permeable materials. In geomorphological terms, there is a large plateau intensively karstified that constitutes the main recharge area. Discharge takes place via a large number of springs, of which the 50 most important add up to a mean spring flow of about 13,500l/s. The active geochemical processes in aquifers of Sierra de Segura, with their corresponding time sequence, are: dissolution of CO2, dissolution of calcite, incongruent dissolution of dolomite, dedolomitization, exsolution of CO2, and precipitation of calcite. More evolved water has higher temperature, magnesium content and Mg/Ca ratio; therefore, these parameters can be utilised as indicators of the degree of hydrochemical evolution. In addition, a good correlation between water temperature and magnesium concentration (or Mg/Ca ratio) indicates that an increase in temperature accelerates the kinetics of the dissolution of dolomite. Finally, the distribution of the temperatures in the vadose zone, determined by atmospheric thermal gradient, implies an apparent stratification of the predominant hydrochemical processes and of the groundwater physical and chemical characteristics.
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Vengosh, A., & Rosenthal, E. (1994). Saline groundwater in Israel: its bearing on the water crisis in the country. Journal of Hydrology, 156(1), 389–430.
Abstract: One of the major causes for the deterioration of water quality bearing heavily on the water crisis in Israel is the ongoing contamination of its water resources by saline water bodies. The present paper reviews the geochemical processes forming saline water, lists and explains certain chemical and isotopic parameters which enable understanding these processes and describes the saline groundwater bodies and various salinization phenomena occurring in the country’s various aquifers. Deterioration of groundwater in Israel is caused by numerous natural processes such as encroachment of sea water, migration of connate, highly pressurized brines penetrating into fresh groundwater, by subsurface dissolution of soluble salts originating in surrounding country rocks and by water-rock interaction. In addition to sea water, two saline water bodies were identified as the main factors causing salinization of fresh groundwater: (a) Ca-chloride brines encountered in the Jordan-Dead Sea Rift Valley, in various parts of the Negev and of the Coastal Plain, and (b) Na-chloride saline water identified in the subsurface of the Negev and in the southern part of the Coastal Plain. Intensive exploitation of groundwater in Israel has disturbed the natural equilibrium which prevailed between fresh and saline water. The newly established groundwater flow regimes have facilitated the migration of saline water bodies, their participation in the active hydrological cycle and the progressive contamination of fresh groundwater. These processes which were not anticipated by planners and water resources managers emphasize that large-scale groundwater exploitation was undertaken without giving sufficient consideration to the occurrence and subsurface migration of saline water and brines.
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