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Jalali*, M., Karami, S., & Marj, A. F. (2019). On the problem of the spatial distribution delineation of the groundwater quality indicators via multivariate statistical and geostatistical approaches. Environ. Monit. Assess., 191(S2), 323.
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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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Lu, C., Xin, P., Kong, J., Li, L., & Luo, J. (2016). Analytical solutions of seawater intrusion in sloping confined and unconfined coastal aquifers. Water Resources Research, 52(9), 6989–7004.
Abstract: Abstract Sloping coastal aquifers in reality are ubiquitous and well documented. Steady state sharp-interface analytical solutions for describing seawater intrusion in sloping confined and unconfined coastal aquifers are developed based on the Dupuit-Forchheimer approximation. Specifically, analytical solutions based on the constant-flux inland boundary condition are derived by solving the discharge equation for the interface zone with the continuity conditions of the head and flux applied at the interface between the freshwater zone and the interface zone. Analytical solutions for the constant-head inland boundary are then obtained by developing the relationship between the inland freshwater flux and hydraulic head and combining this relationship with the solutions of the constant-flux inland boundary. It is found that for the constant-flux inland boundary, the shape of the saltwater interface is independent of the geometry of the bottom confining layer for both aquifer types, despite that the geometry of the bottom confining layer determines the location of the interface tip. This is attributed to that the hydraulic head at the interface is identical to that of the coastal boundary, so the shape of the bed below the interface is irrelevant to the interface position. Moreover, developed analytical solutions with an empirical factor on the density factor are in good agreement with the results of variable-density flow numerical modeling. Analytical solutions developed in this study provide a powerful tool for assessment of seawater intrusion in sloping coastal aquifers as well as in coastal aquifers with a known freshwater flux but an arbitrary geometry of the bottom confining layer.
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Wigley, T. M. L., & Plummer, L. N. (1976). Mixing of carbonate waters. Geochimica et Cosmochimica Acta, 40(9), 989–995.
Abstract: When mineral solutions of different compositions are mixed, the molalities and activities of individual ions in the mixture are often non-linear functions of their end-member values. This non-linearity is particularly significant in determining mineral saturation levels. Mixtures of saturated solutions may be either undersaturated or supersaturated depending on the end-member compositions and the physical conditions in which end-members and their mixtures exist. In carbonate solutions important non-linear effects occur due to redistribution of carbonate species. In extreme cases this causes mixture pH to be below both the end-member pH values. A simple but precise computer program (WATMIX) has been developed for calculating mixture composition for closed and open system mixing of arbitrary end-members. A number of mixing examples are considered which allow one to isolate three important processes leading to non-linear behaviour: the algebraic effect, the δPCO2 effect, and the ionic strength effect.
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Karatas, B. S., Camoglu, G., & Olgen, M. K. (2013). Spatio-temporal trend analysis of the depth and salinity of the groundwater, using geostatistics integrated with GIS, of the Menemen Irrigation System, Western Turkey. Ekoloji, 22(86), 36–47.
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