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Author Mongelli, G.; Monni, S.; Oggiano, G.; Paternoster, M.; Sinisi, R. url  doi
openurl 
  Title Tracing groundwater salinization processes in coastal aquifers: a hydrogeochemical and isotopic approach in the Na-Cl brackish waters of northwestern Sardinia, Italy Type Journal Article
  Year 2013 Publication Hydrology and Earth System Sciences Abbreviated Journal  
  Volume (up) 17 Issue 7 Pages 2917-2928  
  Keywords salinization, isotopes, Sardinia  
  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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  Corporate Author Thesis  
  Publisher Copernicus Place of Publication Editor  
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  Notes Approved no  
  Call Number THL @ christoph.kuells @ hess-17-2917-2013 Serial 79  
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Author Karatas, B.S.; Camoglu, G.; Olgen, M.K. doi  openurl
  Title Spatio-temporal trend analysis of the depth and salinity of the groundwater, using geostatistics integrated with GIS, of the Menemen Irrigation System, Western Turkey Type Journal Article
  Year 2013 Publication Ekoloji Abbreviated Journal  
  Volume (up) 22 Issue 86 Pages 36-47  
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  Notes Approved no  
  Call Number CUT @ phaedon.kyriakidis @ Karatas2013 Serial 145  
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Author Zghibi, A.; Zouhri, L.; Tarhouni, J.; Kouzana, L. url  openurl
  Title Groundwater mineralisation processes in Mediterranean semi-arid systems (Cap-Bon, North east of Tunisia): hydrogeological and geochemical approaches Type Journal Article
  Year 2013 Publication Hydrological Processes Abbreviated Journal  
  Volume (up) 27 Issue 22 Pages 3227-3239  
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  Publisher Wiley Online Library Place of Publication Editor  
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  Notes Approved no  
  Call Number THL @ luqianxue.zhang @ zghibi2013groundwater Serial 73  
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Author Agoubi*, B.; Kharroubi, A.; Abida, H. doi  openurl
  Title Saltwater intrusion modelling in Jorf coastal aquifer, Southeastern Tunisia: geochemical, geoelectrical and geostatistical application Type Journal Article
  Year 2013 Publication Hydrol. Process. Abbreviated Journal  
  Volume (up) 27 Issue Pages 1191-1199  
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  Call Number CUT @ phaedon.kyriakidis @ Agoubi2013 Serial 139  
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Author Daniele, L.; Vallejos, Á.; Corbella, M.; Molina, L.; Pulido-Bosch, A. url  doi
openurl 
  Title Hydrogeochemistry and geochemical simulations to assess water–rock interactions in complex carbonate aquifers: The case of Aguadulce (SE Spain) Type Journal Article
  Year 2013 Publication Applied Geochemistry Abbreviated Journal  
  Volume (up) 29 Issue Pages 43-54  
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  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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  ISSN 0883-2927 ISBN Medium  
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  Notes Approved no  
  Call Number THL @ christoph.kuells @ Daniele2013 Serial 19  
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