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Narany, T. S., Ramli, M. F., Aris, A. Z., Sulaiman, W. N. A., Juahir, H., & Fakharian, K. (2014). Identification of the hydrogeochemical processes in groundwater using classic integrated geochemical methods and geostatistical techniques, in Amol-Babol plain, Iran. Sci. World J., 419058,, 15.
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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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Zhou, X., & Li, C. (1992). Hydrogeochemistry of deep formation brines in the central Sichuan Basin, China. Journal of Hydrology, 138(1), 1–15.
Abstract: Subsurface brines are abundant in the Sichuan Basin, China. Five brine-bearing aquifers have been identified within rocks of Triassic age in the central part of the basin. These are of two types: brine-bearing clastic and brine-bearing carbonate aquifers. Brines in this region have high total dissolved solids and chemical species that are different from those of evaporatively concentrated seawater. Deep formation brines in clastic aquifers, in which evaporites do not exist, are characterized by high concentrations of Ca, Sr, Ba, Br and I, low concentrations of Mg and K, and lack of SO4, and are dominated by the NaCaCl type. Brines in carbonate aquifers, which have interbeds of evaporites, are characterized by high total dissolved solids, low concentrations of Ca, Mg and SO4, and lack of Ba, and are of the NaCl type. The brines in clastic aquifers originate from connate continental sedimentary waters mixed with marine waters; membrane filtration through shales has played an important part in modifying the chemical compositions and increasing the salinity of the brines. Those in carbonate aquifers are bittern marine sedimentary waters, with chemical compositions mainly controlled by precipitation of evaporites.
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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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Daniele, L., Vallejos, Á., Corbella, M., Molina, L., & Pulido-Bosch, A. (2013). Hydrogeochemistry and geochemical simulations to assess water–rock interactions in complex carbonate aquifers: The case of Aguadulce (SE Spain). Applied Geochemistry, 29, 43–54.
Abstract: The hydrogeological unit of Aguadulce (Campo de Dalías aquifers, SE Spain) has a complex geometry. This fact, together with a continuous rise in water demand due to intensive agriculture and tourism create problems for groundwater quantity and quality. In this paper classic geochemical tools managed by means of GIS software and geochemical simulations are combined to delineate, identify and locate the possible physicochemical processes acting in the Aguadulce groundwater. Two main aquifers can be distinguished: the carbonate or lower aquifer of Triassic age, and the calcodetritic or upper aquifer of Plio-Quaternary age. Groundwaters from the latter are more saline and, assuming all chlorinity originates from seawater intrusion, the seawater contribution to their composition would be up to 7%. Nevertheless the carbonate aquifer appears not to be homogeneous: it is compartmentalised into 4 zones where different processes explain the different groundwaters compositions. Zone 4 samples (E margin of the carbonate aquifer) resemble those of the Plio-Quaternary aquifer, where calcite precipitation, dolomite and gypsum dissolution and some cation exchange (water–rock interaction) together with seawater–freshwater mixing occur. In contrast, water–rock interaction predominates in zones 1 and 3 of the carbonate aquifer. Moreover, zone 2 samples, located between zones 1 and 3, are explained by water–rock interaction in addition to mixing with Plio-Quaternary aquifer waters. The combination of geochemical simulations with GIS and hydrogeochemical analyses has proven to be effective in identifying and locating the different physicochemical processes in the aquifer areas, thus improving understanding of hydrogeochemistry in complex aquifers.
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