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Ghabayen, S., McKee, M., & Kemblowski, M. (2006). Ionic and Isotopic Ratios for Identification of Salinity Sources and Missing Data in the Gaza Aquifer. Journal of Hydrology, 318, 360–373.
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Garcia*, L. A., & Shigidi, A. (2006). Using neural networks for parameter estimation in ground water. Hydrogeol. J., 318, 215–231.
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Kim, Y., Lee, K. - S., Koh, D. - C., Lee, D. - H., Lee, S. - G., Park, W. - B., et al. (2003). Hydrogeochemical and isotopic evidence of groundwater salinization in a coastal aquifer: a case study in Jeju volcanic island, Korea. Journal of Hydrology, 270(3), 282–294.
Abstract: In order to identify the origin of saline groundwater in the eastern part of Jeju volcanic island, Korea, a hydrogeochemical and isotopic study has been carried out for 18 observation wells located in east and southeast coastal regions. The total dissolved solid contents of groundwaters are highly variable (77–21,782mg/l). Oxygen, hydrogen, sulfur, and strontium isotopic data clearly show that the saline water results from mixing of groundwater with seawater. Strontium isotopic compositions and Br/Cl and I/Cl ratios strongly suggest that the source of salinity is modern seawater intrusion. Hydrogeochemical characteristics based on bivariate diagrams of major and minor ions show that changes in the chemical composition of groundwater are mainly controlled by the salinization process followed by cation-exchange reactions. The highly permeable aquifers at the east coastal region are characterized by low hydraulic gradient and discharge rate and high hydraulic conductivity as compared with other regions. These properties enhance the salinization of groundwater observed in the study area. Based on the Cl, Br, and δ18O data, seawater was determined to have intruded inland some 2.5km from the coastline. Considering the poor correlation of sampling depth and Cl concentrations observed, the position of seawater-freshwater interface is not uniformly distributed in the study area, due to heterogeneities of the basaltic aquifers.
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Gopinath, S., Srinivasamoorthy, K., Saravanan, K., & Prakash, R. (2019). Tracing groundwater salinization using geochemical and isotopic signature in Southeastern coastal Tamilnadu, India. Chemosphere, 236, 124305.
Abstract: Attempt has been made to discriminate groundwater salinity causes along the east coast of India. A total of 122 groundwater samples (61/season) were collected for two diverse seasons (Pre Monsoon and Post Monsoon) and analyzed for physical and chemical components along with stable isotopes. The Piper diagram proposes samples along the coast predisposed by saltwater incursion. Ionic ratio plots recommend groundwater discriminatory by changing geochemical signatures. The statistical correlation suggests impact of saltwater incursion, anthropogenic and rock water interaction as sources for dissolved constituents in groundwater. The thermodynamic stability plot suggests higher silicate dissolution, weathering and ion exchange prompting water chemistry nevertheless of seasons. The δ 18O and δ 2H increases towards the sea suggesting enrichment attributed to the sea water influence and rainfall influences along the southwestern parts of the study area.
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Stigter, T. Y., van Ooijen, S. P. J., Post, V. E. A., Appelo, C. A. J., & Carvalho Dill, A. M. M. (1998). A hydrogeological and hydrochemical explanation of the groundwater composition under irrigated land in a Mediterranean environment, Algarve, Portugal. Journal of Hydrology, 208(3), 262–279.
Abstract: In the Campina de Faro, in the south of Portugal, agricultural practices have a large impact on groundwater composition. These practices involve pumping of water for irrigation from combinations of large diameter, shallow wells (noras) and small diameter, deep boreholes (furos). Excess irrigation water returns to the aquifer and mixes with water from the regional groundwater flow system. This irrigation return flow is concentrated by strong evapotranspiration and by flushing of fertilisers. The concentration increase induces cation exchange, whereby Ca on the soil exchanger is replaced by Na. The mixing in the aquifer allows application of a mixing cell model which may then be used to calculate transmissivities from the Cl mass balance. The calculations are complicated by the time-variant behaviour of Cl and the method is adjusted to calculate the change of chloride in time. Results from the calculations appear to be in good agreement with hydrochemical observations.
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