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Post, V. E. A. (2018). Annotated translation of “Nota in verband met de voorgenomen putboring nabij Amsterdam [Note concerning the intended well drilling near Amsterdam]” by J. Drabbe and W. Badon Ghijben (1889). Hydrogeology Journal, 26(6).
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Zghibi, A., Zouhri, L., Tarhouni, J., & Kouzana, L. (2013). Groundwater mineralisation processes in Mediterranean semi-arid systems (Cap-Bon, North east of Tunisia): hydrogeological and geochemical approaches. Hydrological Processes, 27(22), 3227–3239.
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Agoubi*, B., Kharroubi, A., & Abida, H. (2013). Saltwater intrusion modelling in Jorf coastal aquifer, Southeastern Tunisia: geochemical, geoelectrical and geostatistical application. Hydrol. Process., 27, 1191–1199.
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Kisi, O., Liepelt, K., & Kulls, C. (2023). Discussion of “Improving Prediction Accuracy of Hydrologic Time Series by Least-Squares Support Vector Machine Using Decomposition Reconstruction and Swarm Intelligence”. Journal of Hydrologic Engineering, 28(4), 07023001.
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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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