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Russak, A., Sivan, O., & Yechieli, Y. (2016). Trace elements (Li, B, Mn and Ba) as sensitive indicators for salinization and freshening events in coastal aquifers. Chemical Geology, 441, 35–46.
Abstract: The current global intrusion of seawater into coastal aquifers causes salinization of groundwater and thus significant degradation of its quality. This study quantified the effect of seawater intrusion and freshening events in coastal aquifers on trace elements (Li, B, Mn and Ba) across the fresh-saline water interface (FSI) and their possible use as indicators for these events. This was done by combining field data and column experiments simulating these events. The experiments enabled quantification of the processes affecting the trace element composition and examination of whether salinization and freshening events are geochemically reversible, which has been seldom investigated. The dominant process affecting trace element composition during salinization and freshening is ion exchange. The results of the experiments show that the concentrations of major cations and Li+ were reversible during salinization and freshening, whereas B, Mn2+ and Ba2+ were not. During salinization, Li+ and B were depleted due to sorption by 10 and 100μmol·L−1, respectively, to about half of their expected conservative concentrations. The relative depletion of Li+ increased with distance from the shore, representing the propagation of salinization. Ba2+ and Mn2+ were desorbed from the sediment during salinization and enriched by tenfold in the aqueous phase compared to their concentration in seawater ( 0.1 μeq·L−1). During freshening both were depleted by almost tenfold compared to their concentration in fresh groundwater ( 0.7 μeq·L−1). The depletion of Mn2+ is a sensitive marker for freshening because Mn2+ has a strong affinity to the solid phase. Moreover, this study shows that both Mn2+ and Ba2+ can be used as sensitive hydrogeochemical tools to distinguish between salinization and freshening events in the FSI zone in coastal aquifers.
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Rina, K., Datta, P. S., Singh, C. K., & Mukherjee, S. (2013). Isotopes and ion chemistry to identify salinization of coastal aquifers of Sabarmati River Basin. Current Science, 104(3), 335–344.
Abstract: The lower reaches of the Sabarmati River Basin in Gujarat have intense agricultural and industrial activities and this part is affected by problems of groundwater salinity. Here we attempt to assess the processes governing the causes of groundwater salinity in the coastal alluvial aquifer, employing δ18O and δD isotopes in integration with ionic ratio. The different hydrochemical facies such Na–Mg–HCO3–Cl, Na–Cl–SO4, Na–Mg–Cl–HCO3–SO4 and Na–Cl of groundwater show the occurrence of complex geochemical phenomenon in the study area. Ionic ratio (such as Mg2+/Ca2+, Na+/Cl−, SO24/Cl-, K+/Cl−) and isotopic composition (δ18O and δD) of groundwater indicate that while in coastal areas seawater intrusion is taking place, in inland areas various anthropogenic activities and overexploitation have induced salinity in groundwater. Over-pumping of groundwater has also induced lateral intermixing of highly saline water in the vicinity of coastal areas with relatively fresh/low saline groundwater along specific flow pathways.
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Tulipano, L., Fidelibus, D. M., & Panagopoulos, A. (Eds.). (2005). Groundwater management of coastal karstic aquifers. EU.
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Siarkos, I., & Latinopoulos, P. (2016). Modeling seawater intrusion in overexploited aquifers in the absence of sufficient data: application to the aquifer of Nea Moudania, northern Greece. Hydrogeology J., 24, 2123–2141.
Abstract: In many coastal areas, overexploitation of groundwater resources has led both to the quantitative degradation of local aquifers and the deterioration of groundwater quality due to seawater intrusion. To investigate the behavior of coastal aquifers under these conditions, numerical modeling is usually implemented; however, the proper implementation of numerical models requires a large amount of data, which are often not available due to the time-consuming and costly process of obtaining them. In the present study, the investigation of the behavior of coastal aquifers under the lack of adequate data is
attempted by developing a methodological framework consisting of a series of numerical simulations: a steady-state, a false-transient and a transient simulation. The sequence and the connection between these simulations constitute the backbone of the whole procedure aimed at adjusting the various
model parameters, as well as obtaining the initial conditions for the transient simulation. The validity of the proposed methodology is tested through evaluation of the model calibration procedure and the estimation of the simulation errors (mean error, mean absolute error, root mean square error, mean relative error) using the case of Nea Moudania basin, northern Greece. Furthermore, a sensitivity analysis is performed in order to minimize the error estimates and thus to maximize the reliability of the models. The results of the whole procedure affirm the proper implementation of the developed methodology under specific conditions and assumptions due to the lack of sufficient data, while they give a clear picture of the aquifer’s quantitative and qualitative status.
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Qi, H., Ma, C., He, Z., Hu, X., & Gao, L. (2019). Lithium and its isotopes as tracers of groundwater salinization: A study in the southern coastal plain of Laizhou Bay, China. Sci Total Environ, 650(Pt 1), 878–890.
Abstract: In the southern coastal plain of Laizhou Bay, due to intensive exploitation of groundwater since the early 1970s, the shallow aquifer has been severely influenced by saltwater intrusion, which causes the extraction to shift from shallow to deeper aquifer changing the hydrogeological condition greatly. This study was conducted to investigate the groundwater salinization using hydrochemistry and H, O and Li isotope data. Dissolved Li shows a linear correlation with Cl and Br in seawater, brine and saline groundwater indicating the marine Li source, whereas the enrichment of Li in surface water, brackish and fresh groundwater is impacted by dissolution of silicate minerals. The analyses of hydrochemistry and isotopes (H, O and Li) indicate that brine originated from seawater evaporation, followed by mixing processes and some water-rock interactions; shallow saline groundwater originated from brine diluted with seawater and fresh groundwater; deep saline groundwater originated from seawater intrusion. The negative correlation of δ(7)Li and Li/Na in surface water, brackish and fresh groundwater is contrary to the general conclusion, indicating the slow weathering of silicate minerals and hydraulic interaction between surface water and shallow groundwater in this area. The analyses of hydrochemistry and isotopes (Li, H and O) can well identify the salinity sources and isotope fractionation in groundwater flow and mixing, especially groundwater with high TDS. As both mixing with saltwater and isotope fractionation can explain the combination of high δ(7)Li and low TDS in brackish groundwater, isotope fractionation may limit their use in recognizing salinity sources of groundwater with low TDS.
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