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Di Lorenzo, T., & Galassi, D. M. P. (2013). Agricultural impact on Mediterranean alluvial aquifers: do groundwater communities respond? Fundamental and Applied Limnology/Archiv für Hydrobiologie, 182(4), 271–282.
Abstract: In Mediterranean countries agricultural development heavily depends on groundwater availability due
to arid and semi-arid climate and poor surface-water resources. Agriculture represents one of the most relevant
pressures which generate impacts in alluvial aquifers by means of fertilizers and pesticides usage and groundwater
overexploitation. Until now, very few studies have addressed the ecological response of groundwater fauna to
groundwater contamination and overexploitation due to agricultural practices. We investigated a Mediterranean
alluvial aquifer heavily affected by nitrates contamination and groundwater abstraction stress due to crop irrigation. The aim of this study was to evaluate the sensitivity of groundwater communities to (a) groundwater nitrate
contamination, (b) groundwater abstraction due to irrigation practices, and (c) saltwater intrusion. The present
work suggests that nitrate concentration lower than 150 mg l
–1 is not an immediate threat to groundwater biodiversity in alluvial aquifers. This conclusion must be carefully considered in the light of the total lack of knowledge
of the effects of long-term nitrate pollution on the groundwater biota. Moreover, local extinctions of less tolerant
species, prior to monitoring, cannot be ruled out. Conversely, species abundances in ground water are affected by
groundwater withdrawal, but species richness may be less sensitive. This result is attributable to the disappearance
of saturated microhabitats and to the depletion of fine unconsolidated sediments, reducing the surface available
to bacterial biofilm, which represent the trophic resource for several groundwater invertebrates and where the
main aquifer self-purification processes, such as denitrification, take place. Saltwater intrusion seems not to affect
groundwater species at the values measured in this coastal aquifer.
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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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Morales-Baquero, R., Pulido-Villena, E., & Reche, I. (2013). Chemical signature of Saharan dust on dry and wet atmospheric deposition in the south-western Mediterranean region. Tellus B: Chemical and Physical Meteorology, 65(1), 18720.
Abstract: We studied if the presence of Saharan dust intrusions and the rains modify the chemical signature of the wet and dry deposition in the southern Iberian Peninsula. We have sorted the 109 sampling weeks by the presence (rainy weeks) or absence (dry weeks) of rain and by the occurrence or not of Saharan dust intrusions. Dry deposition dominated the delivery of particulate material (PM), total phosphorus (TP), soluble reactive phosphorus (SRP), Ca2+, Mg2+ and K+, whereas wet deposition dominated the delivery of Na+, total nitrogen, and . In the dry weeks, the presence of Saharan dust intrusions lead to higher inputs of PM, TP, SRP, Ca2+, Mg2+ and K+ in the dry deposition. Conversely, in the rainy weeks, there were no differences in mean values of dry deposition irrespective of the occurrence of Saharan dust intrusions. Nevertheless, in the presence of Saharan intrusions and some rain, the weekly collection of PM, TP and Ca2+ in dry deposition were significantly higher and increased as rainfall was lower. By contrast, the ions Cl– and Na+ in wet deposition were higher in absence of Saharan dust intrusion and increased as rainfall increased.
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Khaska, M., Salle], C. [L. G. L., Lancelot, J., team, A. S. T. E. R., Mohamad, A., Verdoux, P., et al. (2013). Origin of groundwater salinity (current seawater vs. saline deep water) in a coastal karst aquifer based on Sr and Cl isotopes. Case study of the La Clape massif (southern France). Applied Geochemistry, 37, 212–227.
Abstract: In this study a typical coastal karst aquifer, developed in lower Cretaceous limestones, on the western Mediterranean seashore (La Clape massif, southern France) was investigated. A combination of geochemical and isotopic approaches was used to investigate the origin of salinity in the aquifer. Water samples were collected between 2009 and 2011. Three groundwater groups (A, B and C) were identified based on the hydrogeological setting and on the Cl− concentrations. Average and maximum Cl− concentrations in the recharge waters were calculated (ClRef. and ClRef.Max) to be 0.51 and 2.85mmol/L, respectively). Group A includes spring waters with Cl− concentrations that are within the same order of magnitude as the ClRef concentration. Group B includes groundwater with Cl− concentrations that range between the ClRef and ClRef.Max concentrations. Group C includes brackish groundwater with Cl− concentrations that are significantly greater than the ClRef.Max concentration. Overall, the chemistry of the La Clape groundwater evolves from dominantly Ca–HCO3 to NaCl type. On binary diagrams of the major ions vs. Cl, most of the La Clape waters plot along mixing lines. The mixing end-members include spring waters and a saline component (current seawater or fossil saline water). Based on the Br/Clmolar ratio, the hypothesis of halite dissolution from Triassic evaporites is rejected to explain the origin of salinity in the brackish groundwater. Groundwaters display 87Sr/86Sr ratios intermediate between those of the limestone aquifer matrix and current Mediterranean seawater. On a Sr mixing diagram, most of the La Clape waters plot on a mixing line. The end-members include the La Clape spring waters and saline waters, which are similar to the deep geothermal waters that were identified at the nearby Balaruc site. The 36Cl/Cl ratios of a few groundwater samples from group C are in agreement with the mixing hypothesis of local recharge water with deep saline water at secular equilibrium within a carbonate matrix. Finally, PHREEQC modelling was run based on calcite dissolution in an open system prior to mixing with the Balaruc type saline waters. Modelled data are consistent with the observed data that were obtained from the group C groundwater. Based on several tracers (i.e. concentrations and isotopic compositions of Cl and Sr), calculated ratios of deep saline water in the mixture are coherent and range from 3% to 16% and 0% to 3% for groundwater of groups C and B, respectively. With regard to the La Clape karst aquifer, the extension of a lithospheric fault in the study area may favour the rise of deep saline water. Such rises occur at the nearby geothermal Balaruc site along another lithospheric fault. At the regional scale, several coastal karst aquifers are located along the Gulf of Lion and occur in Mezosoic limestones of similar ages. The 87Sr/86Sr ratios of these aquifers tend toward values of 0.708557, which suggests a general mixing process of shallow karst waters with deep saline fossil waters. The occurrence of these fossil saline waters may be related to the introduction of seawater during and after the Flandrian transgression, when the highly karstified massifs invaded by seawater, formed islands and peninsulas along the Mediterranean coast.
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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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