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Abstract: Throughout the Mediterranean, salinization threatens water quality, especially in coastal areas. This salinization is the result of concomitant processes related to both seawater intrusion and water–rock interaction, which in some cases are virtually indistinguishable. In the Nurra region of northwestern Sardinia, recent salinization related to marine water intrusion has been caused by aquifer exploitation. However, the geology of this region records a long history from the Palaeozoic to the Quaternary, and is structurally complex and comprises a wide variety of lithologies, including Triassic evaporites. Determining the origin of the saline component of the Jurassic and Triassic aquifers in the Nurra region may provide a useful and more general model for salinization processes in the Mediterranean area, where the occurrence of evaporitic rocks in coastal aquifers is a common feature. In addition, due to intensive human activity and recent climatic change, the Nurra has become vulnerable to desertification and, in common with other Mediterranean islands, surface water resources periodically suffer from severe shortages. With this in mind, we report new data regarding brackish and surface waters (outcrop and lake samples) of the Na-Cl type from the Nurra region, including major ions and selected trace elements (B, Br, I, and Sr), in addition to isotopic data including δ18O, δD in water, and δ34S and δ18O in dissolved SO4. To identify the origin of the salinity more precisely, we also analysed the mineralogical and isotopic composition of Triassic evaporites. The brackish waters have Cl contents of up to 2025 mg L−1 , and the ratios between dissolved ions and Cl, with the exception of the Br / Cl ratio, are not those expected on the basis of simple mixing between rainwater and seawater. The δ18O and δD data indicate that most of the waters fall between the regional meteoric water line and the global meteoric water line, supporting the conclusion that they are meteoric in origin. A significant consequence of the meteoric origin of the Na-Cl-type water studied here is that the Br / Cl ratio, extensively used to assess the origin of salinity in fresh water, should be used with care in carbonate aquifers that are near the coast. Overall, δ34S and δ18O levels in dissolved SO4 suggest that water–rock interaction is responsible for the Na-Cl brackish composition of the water hosted by the Jurassic and Triassic aquifers of the Nurra, and this is consistent with the geology and lithological features of the study area. Evaporite dissolution may also explain the high Cl content, as halite was detected within the gypsum deposits. Finally, these Na-Cl brackish waters are undersaturated with respect to the more soluble salts, implying that in a climate evolving toward semi-arid conditions, the salinization process could intensify dramatically in the near future.
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Han, D., & Currell, M. J. (2018). Delineating multiple salinization processes in a coastal plain aquifer, northern China: hydrochemical and isotopic evidence. Hydrology and Earth System Sciences, 22(6), 3473–3491.
Abstract: Groundwater is an important water resource for agricultural irrigation and urban and industrial utilization in the coastal regions of northern China. In the past 5 decades, coastal groundwater salinization in the Yang–Dai river plain has become increasingly serious under the influence of anthropogenic activities and climatic change. It is pivotal for the scientific management of coastal water resources to accurately understand groundwater salinization processes and their causative factors. Hydrochemical (major ion and trace element) and stable isotopic (δ18O and δ2H) analysis of different water bodies (surface water, groundwater, geothermal water and seawater) were conducted to improve understanding of groundwater salinization processes in the plain's Quaternary aquifer. Saltwater intrusion due to intensive groundwater pumping is a major process, either by vertical infiltration along riverbeds which convey saline surface water inland, and/or direct subsurface lateral inflow. Trends in salinity with depth indicate that the former may be more important than previously assumed. The proportion of seawater in groundwater is estimated to have reached up to 13 % in shallow groundwater of a local well field. End-member mixing calculations also indicate that the geothermal water with high total dissolved solids (up to 10.6 g L−1) with depleted stable isotope compositions and elevated strontium concentrations (> 10 mg L−1) also mixes locally with water in the overlying Quaternary aquifers. This is particularly evident in samples with elevated Sr ∕ Cl ratios (> 0.005 mass ratio). Deterioration of groundwater quality by salinization is also clearly exacerbated by anthropogenic pollution. Nitrate contamination via intrusion of heavily polluted marine water is evident locally (e.g., in the Zaoyuan well field); however, more widespread nitrate contamination due to other local sources such as fertilizers and/or domestic wastewater is evident on the basis of NO3 ∕ Cl ratios. This study provides an example of how multiple geochemical indicators can delineate different salinization processes and guide future water management practices in a densely populated water-stressed coastal region.
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Gaye, C. B. (2001). Isotope techniques for monitoring groundwater salinization. Hydrogeology Journal, 9, 217–218.
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Cary, L., Petelet-Giraud, E., Bertrand, G., Kloppmann, W., Aquilina, L., Martins, V., et al. (2015). Origins and processes of groundwater salinization in the urban coastal aquifers of Recife (Pernambuco, Brazil): a multi-isotope approach. Science of the Total Environment, 530-531, 411–429.
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Araguás-Araguás, L. (2003). Identification of the mechanisms and origin of salinization of groundwater in coastal aquifers by isotope techniques. Tecnología de la intrusión de agua de mar en acuíferos costeros, Países Mediterráneos, , 365–371.
Abstract: When assessing the origin of salinity and the mechanisms of salinization in coastal aquifers, hydrogeologists may consider the combined use of certain geochemical tools to assess critical aspects of the hydrogeological setting of the system. These tools are based in the integrated use of chemical (major ions, trace elements and ionic ratios) and isotope parameters (oxygen, hydrogen, sulphur, carbon, strontium and boron). The problem of groundwater salinization in coastal aquifers, besides active seawater intrusion, may be affected by several human activities that accelerate the progressive deterioration of water quality, such as concentrated pumping, intensive agricultural practices including return flows or reuse of waste waters from urban or industrial origin. The characterisation of the perating processes and mechanisms of salinization is a requisite for a proper management of groundwater resources and for adopting remediation strategies. In this contribution the potential role of several isotopic tools in these studies is briefly described.
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