Recharge of the plio-quaternary water table aquifer in Tunisian chotts region estimated from stable isotopes

The hydrodynamic groundwater data and stable isotopes of water have been used jointly for better understanding of upward leakage and mixing processes in the Djerid aquifer system (southwestern Tunisia). The aquifer system is composed of the upper unconfined Plio-Quaternary (PQ) aquifer, the intermediate (semi-)confined Complex Terminal (CT) aquifer and the deeper confined Continental Intercalaire (CI) aquifer. A total of 41 groundwater samples from the CT and PQ aquifers were collected during June 2001. The stable isotope composition of waters establishes that the CT deep groundwater (depleted as compared to present Nefta local rainfall) is ancient water recharged during late Quaternary time. The relatively recent water in the shallow PQ aquifer is composed of mixed water resulting from upward leakage and sporadic meteoric recharge. In order to characterize the meteoric input signal for PQ in the study area, rainfall water samples were collected during 4 years (2000–2003) at the Nefta meteorological station. Weighted mean values of isotopic contents with respect to rainfall amounts have been computed. Despite the short collection period in the study area, results agree with those found in Beni Abbes (southwestern Algerian Sahara) by Fontes on 9 years of rainfall surveillance. Stable isotopic relationships provide clear evidence of shallow PQ aquifer replenishment by deep CT groundwater. The ¹⁸O/upward leakage rate allowed the identification of distinctive PQ waters related to CT aquifer configuration (confined in the western part of the study area, semi-permeable in the eastern part). These trends were confirmed by the relation ¹⁸O/TDS. The isotope balance model indicated a contribution of up to 75% of the deep CT groundwater to the upper PQ aquifer in the western study area, between Nefta and Hazoua.     

Quantifying regional groundwater flow between Continental Intercalaire and Djeffara aquifers in southern Tunisia using isotope methods

Large-scale interaction between the Continental Intercalaire and the Djeffara aquifer systems in the southeast of Tunisia has been investigated with the aid of chemical and isotopic tracers. Two distinct groundwater types have been identified: (1) the Continental Intercalaire groundwater characterized by elevated temperatures (50–61.4°C), low δ¹⁸O (−8.4 to−7.87) and δ²H (−67.2 to−59) values and negligible radiocarbon content, both testifying its great age dating from the late Pleistocene period, and (2) the Djeffara groundwater with distinctly heavier isotopic composition (δ¹⁸O = −8.31 to −5.80, δ²H = −65.9 to −31.9). The Djeffara groundwaters reveal a distinct changes of physico-chemical and isotopic parameters near El Hamma Faults in the northwestern part of the Djeffara basin. These changes could possibly be explained by a vertical leakage from the Continental Intercalaire aquifer through El Hamma Faults. The mixing proportions inferred from stable isotope mass balance prove that the contribution of the Continental Intercalaire to the recharge of Djeffara aquifer is very significant and may reach 100% in the El Hamma region and in the northern part of Gabes. Isotope tracers strongly suggest that recent recharge to the Djeffara aquifer system is very limited. Its current yield, particularly in its central and northern parts can be maintained only thanks to large-scale underground inflow from the Continental Intercalaire aquifer system, which carries late Pleistocene palaeowater. Consequently, current exploitation of groundwater resources of the Djeffara aquifer has non-sustainable character.     

Hydrogeological and mixing process of waters in deep aquifers in arid regions: south east Tunisia

This study addresses the hydrogeochemistry of thermal and cold waters from south east Tunisia. Temperature intervals are 38.5–68 °C and 22–27.8 °C for thermal water and cold water, respectively. Three distinct hydrogeological systems supply water either for irrigation or for drinking; they are: (1) the Continental Intercalaire geothermal aquifer (CI), (2) the Turonian aquifer and (3) the Senonian aquifer. A synthetic study including hydrochemical, hydrogeological and geothermal approaches have been applied in order to evaluate the inter-aquifers water transfer in south east of Tunisia. By using silica geothermometers and saturation indices for different solid phases, estimated thermal reservoir temperature varies between 52 and 87 °C and between 75 and 110 °C, respectively. Based on chemical and thermal data, mixing, which occurs between the ascending deep geothermal water and shallow cold water, is about 57 % cold water.     

Hydrochemistry and geothermometry of thermal groundwater of southeastern Tunisia (Gabes region)

Given the vital importance of water and energy in desert regions, we undertook a study dealing with the deep reservoirs in Gabes area, which is located in the southeastern part of Tunisia. Geothermal resources are taken from the Intercalary Continental [or Continental Intercalaire (CI)], known as the largest deep aquifer in Tunisia and are used in a number of applications, mainly in agriculture. Previous investigations performed on the thermal waters of this area focused on the genesis of the deep waters with regard to the thermal features of geothermal reservoirs. A more detailed investigation has been carried out, considering both deep and shallow waters. In order to estimate the potential temperatures of deep reservoir in the Gabes area, we developed a synthetic study including chemical geothermometers, multiple mineral equilibrium approach, and other approaches. Chemical types of the thermal waters and effects of mixing between shallow cold waters with deep thermal waters were also discussed. In fact, the application of Na–K–Mg diagram relative to deep geothermal reservoir capitulate estimated temperatures (about 90°C). In addition, the multiple mineral equilibrium approach submits a similar estimated temperature ranging between 65 and 70°C, showing a disequilibrium status which indicates a possibly mixing with surface water. Indeed, wells exploiting the CI aquifer in the south part of the studied area showed the same characteristics, corroborating the reliability of the applied methods.     

Characterization of Continental Intercalaire aquifer (CI) in the Tinrhert-East Area-Illizi Basin on the Algerian-Libyan Border

This paper addresses the characterization of the Continental Intercalaire aquifer (CI) in the Tinrhert-East area of Illizi Basin on the Algerian-Libyan border, which belongs to the SASS1 system, one of the biggest transboundary aquifers in the world. This study concerns a superficies of 4 300 km2. On the basis of Mud Logging borehole data conducted in this part of the aquifer, a realistic characterization of the aquifer was done. The thickness of the CI aquifer varies from 300 m in the south to 700 m in the north, and the depth ranges from 180 m to 320 m. The interpretation of the logs showed that the aquifer is characterized by a maximum net thickness in its southwestern part (more than 600 m), the porosity is very high, ranging from 30% in the west to 24% at the Libyan borders, the permeability is low to medium around 10-5 m/s, and the maximum transmissivity values of about 8×10-3 m2/s were recorded at the center of the study area. The depth of water varies from 235 m to 312 m, and the water flows from south to north, in accordance with the general direction observed in the CI aquifer in the Northern Sahara Aquifer System (SASS). The porosity values obtained from the interpretation of the sonic and density logs permit to estimate the water reserves of this aquifer considered fossil, at thresholds much higher than what was considered until now.     

Hydrochemical and isotopic behaviour of a Saharan phreatic aquifer suffering severe natural and anthropic constraints (case of Oued-Souf region, Algeria)

An approach combining the use of water dissolved chemical species and isotopic fingerprints has been used to understand the behavior of a phreatic aquifer and to determine the origin of its different water components. This aquifer is located in the large sedimentary basin of the Great Oriental Erg (Algeria) and overlies two deeper aquifers: the Complexe Terminal (CT) and the Continental Intercalaire (CI). Besides the deterioration of its groundwater quality, its water table has risen during the last 20 years. A water budget surplus between 950 and 2500 l s^?1 was estimated. Down-gradient groundwater evolution (south-north) has shown that the mineralisation increases from 1.23 to 5.20 g l^?1 due to evaporite minerals dissolution. Chemical and isotopic data demonstrated that in addition to rainfall there is a contribution from the CT and CI aquifers. The latter are tritium-free and less mineralized than the phreatic aquifer. Their radiocarbon contents are very low (<10 pmC, percent modern Carbon) (Pleistocene recharge) whereas quite the contrary is observed for the superficial aquifer which exhibits fairly high and variable C-14 activities (50–100 pmC), evidence of recent recharge. On the basis of tritium contents, two groundwater groups were identified for the phreatic aquifer.     

Hydrologic and geologic factors controlling groundwater geochemistry in the Turonian aquifer (southern Tunisia)

Water in the fissured limestone and dolomite of the Turonian aquifer of Tunisia has been investigated using geochemical (major ions) and isotopic (δ¹⁸O, δ²H, ¹⁴C) data. To carry out a characterization of aquifer behaviour, 48 representative samples were collected at the end of the humid season. The evolution of chemical composition of groundwater from recharge areas to discharge areas is characterized by increasing sodium, chloride and sulphate contents as a result of leaching of evaporite rock. In the study, three distinct chemical trends in groundwater were identified. The major reactions responsible for the chemical evolution of groundwater in the investigated area fall into three categories: (1) calcite precipitation, (2) gypsum and halite dissolution, and (3) ion exchange. The stable isotope composition of water samples indicates large-scale interaction between the Continental Intercalaire and the Turonian aquifer and the presence of a young local component which probably enters the system via faults and/or fractures.     

Deciphering interaction of regional aquifers in Southern Tunisia using hydrochemistry and isotopic tools

Groundwater is the most important source of water supply in southern Tunisia. Previous hydrogeologic and isotopic studies carried out in this region revealed the existence of two major aquifer systems: the “Complex Terminal” (CT) and the “Continental Intercalaire” (CI). Turonian carbonates constitute one of the major aquifer levels of the CT multilayered aquifer. It extends over most of southern Tunisia, and its hydrodynamic regime is largely influenced by tectonics, lithology and recharge conditions. Forty-eight groundwater samples from the CI and Turonian aquifers were collected between January and April 2004 for chemical and isotopic analyses. Hydrochemistry and isotopic tools were combined to get an insight into the processes controlling chemical composition of groundwater and wide-scale interaction of these two aquifer systems. Analysis of the dissolved constituents revealed that several processes control the observed chemical composition: (i) incongruent dissolution of carbonate minerals, (ii) dissolution of evaporitic minerals, and (iii) cation exchange. Dissolution alone cannot account for the observed high supersaturation states of groundwater with respect to calcite and dolomite. The observed supersaturation is most probably linked to geogenic CO₂ entering water-bearing horizons of the CT and CI aquifers via deep tectonic faults and discontinuities and subsequent degassing in the exploitation wells. Presence of geogenic CO₂ in the investigated region was confirmed by C isotope data of the DIC reservoir. The radiocarbon content of the Turonian samples varied between 9.5 and 43 pmc. For CI samples generally lower values were recorded, between 3.8 and 22.5 pmc. Stable isotope composition of Turonian groundwater samples varied from −8.3 to −5.3‰ for δ¹⁸O and from −60 to −25‰ for δ²H. The corresponding ranges of δ values for the Continental Intercalaire samples were from −8.9‰ to −6.9‰ for δ¹⁸O and from −68.2‰ to −45.7‰ for δ²H. Stable isotope composition of groundwater representing CT and CI aquifers provide strong evidence for regional interaction between both systems.     

Salinisation origin and hydrogeochemical behaviour of the Djerid oasis water table aquifer (southern Tunisia)

The shallow Plio-Quaternary (PQ) water table, present over almost the whole Djerid and Chott El Gharsa basins (southern Tunisia), is used as a complement of oases irrigation, especially in summer season. The simplicity of the Plio-Quaternary lithology is confronted to the complexity of the mineralisation mechanisms and the water origin in this aquifer. An approach combining the use of water-dissolved chemical species and isotopic contents has been used to better understand the PQ behaviour under severe increasing exploitation and to determinate the origin of its different water bodies. In southern Tunisia, the aquifer system is composed of the upper unconfined PQ aquifer, the intermediate semi-confined/confined Complexe Terminal (CT) and the deeper confined Continental Intercalaire (CI). Chemical analyses highlighted an origin of mineralisation in close relationship to the dissolution of both sulphated salts (MgSO₄ and Na₂SO₄) and chlorinated salts (NaCl and MgCl) abundant in the surface and subsurface gypsum crust. Positive correlations between gypsum anhydrite, mirabilite, thenardite and halite saturation indexes with respective mineral species, confirm evaporites dissolutions. Isotopic data showed that in addition of sporadic rainfall events, there is a contribution from the CI and the CT Saharan groundwaters, recharging the PQ aquifer in the study area. Return flow irrigation is partly affected by evaporation, before recharging the shallow aquifer, in oases limits.     

The hydro geochemical characterization of ground waters in Tunisian Chott’s region.

Tunisian Chott’s region is one of the most productive artesian basins in Tunisia. It is located in the southwestern part of the country, and its groundwater resources are developed for water supply and irrigation. The chemical composition of the water is strongly influenced by the interaction with the basinal sediments and by hydrologic characteristics such as the flow pattern and time of residence. The system is composed of an upper unconfined “Plio-Quaternary” aquifer with a varying thickness of 20–200 m, an intermediate confined/unconfined “Complex Terminal” aquifer about 100 m in thickness and a deeper “Continental Intercalaire” aquifer about 150 m in thickness separated by thick clay and marl layers. The dissolution of evaporites and carbonates explains part of the contained Na⁺, Ca²⁺, Mg²⁺, K⁺, SO₄²⁻ and Cl^-, but other processes, such carbonate precipitation, also contributes to the water composition. The stable isotope composition of waters establishes that the deep groundwater (depleted as compared to present corresponding local rainfall) is ancient water recharged probably during the late Pleistocene and the early Holocene periods. The relatively recent water in the Plio-Quaternary aquifer is composed of mixed waters resulting presumably from upward leakage from the deeper groundwater.     

Characterising groundwater and surface-water interconnections using hydrogeology,hydrochemistry and stable isotopes in the Ouémé Delta,southern Benin

The Mio-Pliocene aquifer of the coastal sedimentary basin of Benin is the most exploited aquifer for water supply to the urbanised region in the southern part of the country. The population explosion is putting increasing pressure on quantitative and qualitative aspects of the groundwater resources. Preventing groundwater contamination caused by surface waters requires a thorough understanding of surface-water/groundwater interactions, especially the interactions between the Mio-Pliocene aquifer and surface waters. This study aimed to investigate the interactions between groundwater and surface waters along the major rivers (Sô River and Ouémé Stream) and brooks in the Ouémé Delta. Field campaigns identified 75 springs located in the valleys which feed the rivers, and thus maintain their base flow. The piezometric results indicated, through flow direction assessment, that the Mio-Pliocene aquifer feeds Ouémé Stream and Sô River. Chemical analyses of groundwater and surface waters show similar chemical facies, and changes in the chemical composition in groundwater are also observed in the surface waters. Moreover, the isotopic signatures of surface waters are similar to those of the groundwater and springs, which led to the identification of potential groundwater discharge areas. As a result of groundwater discharge into surface waters, the fraction of groundwater in the surface water is more than 66% in the brooks, regardless of the season. In the Ouémé Stream and Sô River, the fraction of groundwater is 0–21% between June and September, while from October to March it is 47–100%.

     

The recharge of glacial meltwater and its influence on the geochemical evolution of groundwater in the Ordovician-Cambrian aquifer system,northern part of the Baltic Artesian Basin

The geochemical evolution of groundwater in the Ordovician-Cambrian aquifer system in the northern part of the Baltic Artesian Basin (BAB) illustrates how continental glaciations have influenced groundwater systems in proglacial areas. The aquifer system contains water that has originated from various end-members: recent meteoric water, glacial meltwater and relict Na-Cl brine. The saline formation water that occupied the aquifer system prior to the glacial meltwater intrusion has been diluted by meltwaters of advancing-retreating ice sheets. The diversity in the origin of groundwater in the aquifer system is illustrated by a wide variety in δ¹⁸O values that range from −11‰ to −22.5‰. These values are mostly depleted with respect to values found in modern precipitation in the area. The chemical and isotopic composition of groundwater has been influenced by mixing between waters originating from different end-members. In addition, the freshening of a previously saline water aquifer due to glacial meltwater intrusion has initiated various types of water-rock interaction (e.g. ion exchange, carbonate mineral dissolution).     

The geochemical and isotopic composition of aquifer systems in the deltaic region of the Po River plain (northern Italy)

The chemical and hydrodynamic characteristics of groundwater in deltaic regions are strongly influenced by the complex stratigraphy of these areas, caused by the continuously varying depositional environments associated with their recent hydrographic evolution. As a case study, the eastern sector of the Po River plain, northern Italy, has been investigated to understand the quality of the available groundwater resources. Based on the analysis of hydrochemical and isotopic data, the recharge characteristics, the groundwater residence time and the aquifer vulnerability are defined. The results show significant qualitative degradation of the unconfined aquifer due to the shallow depth to water, while in the underlying confined aquifer, a hydrochemical facies of Ca–HCO₃ type prevails. The spatial variation and relationship between oxygen-18 and deuterium determine: firstly, hydraulic separation of the two hydrogeological units; secondly, direct infiltration of local precipitation to the unconfined aquifer; thirdly, the occurrence of waters originating in the Alps and locally from the Apennines, pervading the confined aquifer. The tritium results suggest local mixing between the superficial waters and the confined aquifer, occurring along the palaeo-river channels. This increases the pollution vulnerability of the confined hydrogeological unit within the plain, which is the only natural groundwater resource exploited for water supply.     

川东槽谷区岩溶泉水物理化学动态特征及其环境效应研究——以重庆青木关岩溶槽谷姜家泉为例

以重庆青木关岩溶槽谷姜家泉野外观测试验基地为例,利用CTDP300多参数水质自动记录仪、NITRATAX plussc在线硝氮分析仪及HOBO小型气象站,分别对岩溶泉在不同降雨条件下水化学的动态变化特征进行了监测研究。结果表明:岩溶泉水pH值受偏酸性雨水的影响而降低;水温变化取决于降雨量、持续时间及气温等因素影响。分析认为,电导率的变化随环境的不同而不同,一般降雨环境下雨水的稀释作用仅表现在降雨的开始阶段,之后裂隙含水介质起主要作用;暴雨环境下雨水的稀释作用贯穿整个降雨过程,地下河水质主要受岩溶管道裂隙控制,水动力作用占主要地位。NO3-含量与电导率变化呈正相关,都与降雨量密切相关,从而说明降雨是导致岩溶区土壤元素流失的主要原因,也是造成岩溶山区地下水污染的重要原因。岩溶泉水化学动态变化的监测研究对于解决岩溶石山区居民的饮水、水土保持及石漠化治理具有重要意义。     

Geochemical and isotopic investigation of the aquifer system in the Djerid-Nefzaoua basin, southern Tunisia

In the Djerid-Nefzaoua region, southern Tunisia, about 80% of agricultural and domestic water supply is provided by the complex terminal (CT) aquifer. However, 20% of this demand is provided by other hydraulically connected aquifers, namely the continental intercalaire (CI) and the Plio-Quaternary (PQ). Overexploitation of the CT aquifer for agricultural practices has contributed to the loss of the artesian condition and the decline of groundwater level which largely increased the downward leakage from the shallow PQ aquifer. Excess irrigation water concentrates at different rates in the irrigation channels and in the PQ aquifer itself. Then, it returns to the CT aquifer and mixes with water from the regional flow system, which contributes to the salinization of the CT groundwater. A geochemical and isotopic study had been undertaken over a 2-years period in order to investigate the origin of waters pumped from the CT aquifer with an emphasis on its hydraulic relationships with the underlying and the overlying CI and PQ aquifers. Geochemistry indicates that groundwater samples collected from different wells show an evolution of the water types from Na-Cl to Ca-SO₄-Cl. Dissolution of halite, gypsum and anhydrite-bearing rocks is the main mechanism that leads to the salinization of the groundwater. Isotopic data indicate the old origin of all groundwater in the aquifer system. Mixing and evaporation effects characterizing the CT and the PQ aquifers were identified using δ²H and δ¹⁸O relationship and confirmed by the conjunction of δ²H with chloride concentration.     

Geochemical evolution of groundwater in southern Bengal Basin: The example of Rajarhat and adjoining areas,West Bengal,India

Detailed geochemical analysis of groundwater beneath 1223 km² area in southern Bengal Basin along with statistical analysis on the chemical data was attempted, to develop a better understanding of the geochemical processes that control the groundwater evolution in the deltaic aquifer of the region. Groundwater is categorized into three types: ‘excellent’, ‘good’ and ‘poor’ and seven hydrochemical facies are assigned to three broad types: ‘fresh’, ‘mixed’ and ‘brackish’ waters. The ‘fresh’ water type dominated with sodium indicates active flushing of the aquifer, whereas chloride-rich ‘brackish’ groundwater represents freshening of modified connate water. The ‘mixed’ type groundwater has possibly evolved due to hydraulic mixing of ‘fresh’ and ‘brackish’ waters. Enrichment of major ions in groundwater is due to weathering of feldspathic and ferro-magnesian minerals by percolating water. The groundwater of Rajarhat New Town (RNT) and adjacent areas in the north and southeast is contaminated with arsenic. Current-pumping may induce more arsenic to flow into the aquifers of RNT and Kolkata cities. Future large-scale pumping of groundwater beneath RNT can modify the hydrological system, which may transport arsenic and low quality water from adjacent aquifers to presently unpolluted aquifer.     

A Geochemical study of the groundwater in the Misli basin and environmental implications

The aim of this study was to determine geochemical properties of groundwater and thermal water in the Misli Basin and to assess thermal water intrusion into shallow groundwater due to over-extraction. According to isotope and hydrochemical analyses results, sampled waters can be divided into three groups: cold, thermal, and mixed waters. Only a few waters reach water–rock chemical equilibrium. Thermal waters in the area are characterized by Na⁺–Cl⁻–HCO₃⁻, while the cold waters by CaHCO₃ facies. On the basis of isotope results, thermal waters in the Misli basin are meteoric origin. In particular, δ¹⁸O and δ²H values of shallow groundwater vary from −10.2 to −12.2‰ and −71.2 to −82‰, while those of thermal waters range from −7.8 to −10.1‰ and from −67 to −74‰, respectively. The tritium values of shallow groundwater having short circulation as young waters coming from wells that range from 30 to 70 m in depth vary from 10 to 14 TU. The average tritium activity of groundwater in depths more than 100 m is 1.59 ± 1.16, which indicates long circulation. The rapid infiltration of the precipitation, the recycling of the evaporated irrigation water, the influence of thermal fluids and the heterogeneity of the aquifer make it difficult to determine groundwater quality changes in the Misli Basin. Obtained results show that further lowering of the groundwater table by over-consumption will cause further intrusion of thermal water which resulted in high mineral content into the fresh groundwater aquifer. Because of this phenomenon, the concentrations of some chemical components which impairs water quality in terms of irrigation purposes in shallow groundwaters, such as Na⁺, B, and Cl⁻, are highy probably expected to increase in time.     

Recharge,geochemical processes and water quality in karst aquifers: Central West Bank,Palestine

The Central West Bank aquifer (CWB) is one of the most important resources of fresh groundwater of Palestine. The geology of the area consists mainly of karstic and permeable limestones and dolomites interbedded with argillaceous beds of late Albian–Turonian age. Exploitation of the CWB aquifer, combined with lack of information required to understand the groundwater pattern, represents a challenge for reservoir management. The present work reports hydrogeochemistry, microbiology and environmental isotope data from spring water samples, which were utilized to understand recharge mechanisms, geochemical evolution and renewability of groundwater in CWB aquifer. Besides the major chemical compositions, ionic ratios were used to delineate mineral-solution reactions and weathering processes. Interpretation of chemical data suggests that the chemical evolution of groundwater is primarily controlled by (1) water–rock interactions, involving dissolution of carbonate minerals (calcite and dolomite), and (2) cation exchange processes. The measured equation of the local meteoric water line is δD?=?5.8 δ¹⁸O?+?9.9. Stable isotopes show that precipitation is the source of recharge to the groundwater system. The evaporation line has a linear increasing trend from south to north direction in the study area. All analyzed spring waters are suitable for irrigation, but not for drinking purposes. The results from this study can serve as a basis for decision-makers and stakeholders, with the intention to increase the understanding of sustainable management of the CWBs.     

浅谈长春市地下水水质污染现状及其发展趋势

通过历时13年的长春市地下水水质的监测工作,对长春市地下水污染现状及污染趋势作了分析,结果表明,长春市潜水污染重,化学组合中Cl~-、SO_4~(2-)、NO_3~-、COD、总硬度、矿化度在很多地方出现高含量,且上升趋势明显;承压水在市中心集中开采地污染,其它地区尚未污染或污染较轻。并提出五点防止地下水污染的对策性意见。     

Hydrogeology and geochemistry of the multilayered confined aquifer of the Pisa plain (Tuscany – central Italy)

The Pisa plain contains a multilayered confined aquifer made up of Pleistocene sands and gravels. The groundwater from the wells tapping these horizons are generally of poor quality: they exhibit significant TDS, relatively high Cl content and considerable hardness. During geothermal prospecting of the Pisa plain, about 80 wells ranging in depth from 20 to 250 m were sampled, and both chemical (major ions) and isotope analyses were conducted. The data collected show that TDS is strongly influenced by HCO₃ and Cl, and that a 3-component mixing process affects the groundwater’s chemical composition. The end members of this mixing process have been identified as: (a) diluted HCO₃ meteoric water, which enters the plain mainly from the eastern and northern sides of the study area; (b) Cl-rich water, which largely characterizes the shallow sandy horizons of the multilayered aquifer system and has been attributed to the presence of seawater, as also suggested by δ¹⁸O data; and (c) SO₄-rich groundwater, which is linked to the hot groundwater circulation within Mesozoic carbonate formations and, at first sight, seemed to affect only the gravelly aquifer. A SO₄-rich water also contributes to the sandy aquifer; it probably enters the plain both laterally, from the margins of the Pisan Mountains and from depth, but promptly undergoes substantial SO₄ reduction processes by bacteria. That such processes are at work is suggested both by the low SO₄ and high HCO₃ concentrations found in the well waters and by their C and S isotope compositions. The collected data have allowed zones with higher quality waters to be identified, which may someday be used for the local water supply.