Isotope–geochemical characterization and geothermometrical modeling of Uttarakhand geothermal field,India

Uttarakhand geothermal area, located in the central belt of the Himalayan geothermal province, is one of the important high temperature geothermal fields in India. In this study, the chemical characteristics of the thermal waters are investigated to identify the main geochemical processes affecting the composition of thermal waters during its ascent toward the surface as well as to determine the subsurface temperature of the feeding reservoir. The thermal waters are mainly Ca–Mg–HCO₃ type with moderate silica and TDS concentrations. Mineral saturation states calculated from PHREEQC geochemical code indicate that thermal waters are supersaturated with respect to calcite, dolomite, aragonite, chalcedony, quartz (SI > 0), and undersaturated with respect to gypsum, anhydrite, and amorphous silica (SI < 0). XRD study of the spring deposit samples fairly corroborates the predicted mineral saturation state of the thermal waters. Stable isotopes (δ¹⁸O, δ²H) data confirm the meteoric origin of the thermal waters with no oxygen-18 shift. The mixing phenomenon between thermal water with shallow ground water is substantiated using tritium (³H) and chemical data. The extent of dilution is quantified using tritium content of thermal springs and non-thermal waters. Classical geothermometers, mixing model, and multicomponent fluid geothermometry modeling (GeoT) have been applied to estimate the subsurface reservoir temperature. Among different classical geothermometers, only quartz geothermometer provide somewhat reliable estimation (96–140 °C) of the reservoir temperature. GeoT modeling results suggest that thermal waters have attained simultaneous equilibrium with respect to minerals like calcite, quartz, chalcedony, brucite, tridymite, cristobalite, talc, at the temperature 130 ± 5 °C which is in good agreement with the result obtained from the mixing model.     

A hydrochemical study of the Hammam Righa geothermal waters in north-central Algeria

This study focuses on the hydrochemical characteristics of 47 water samples collected from thermal and cold springs that emerge from the Hammam Righa geothermal field, located in north-central Algeria. The aquifer that feeds these springs is mainly situated in the deeply fractured Jurassic limestone and dolomite of the Zaccar Mount. Measured discharge temperatures of the cold waters range from 16.0 to 26.5 °C and the hot waters from 32.1 to 68.2 °C. All waters exhibited a near-neutral pH of 6.0–7.6. The thermal waters had a high total dissolved solids (TDS) content of up to 2527 mg/l, while the TDS for cold waters was 659.0–852.0 mg/l. Chemical analyses suggest that two main types of water exist: hot waters in the upflow area of the Ca–Na–SO₄ type (Hammam Righa) and cold waters in the recharge zone of the Ca–Na–HCO₃ type (Zaccar Mount). Reservoir temperatures were estimated using silica geothermometers and fluid/mineral equilibria at 78, 92, and 95 °C for HR4, HR2, and HR1, respectively. Stable isotopic analyses of the δ¹⁸O and δD composition of the waters suggest that the thermal waters of Hammam Righa are of meteoric origin. We conclude that meteoric recharge infiltrates through the fractured dolomitic limestones of the Zaccar Mount and is conductively heated at a depth of 2.1–2.2 km. The hot waters then interact at depth with Triassic evaporites located in the hydrothermal conduit (fault), giving rise to the Ca–Na–SO₄ water type. As they ascend to the surface, the thermal waters mix with shallower Mg-rich groundwater, resulting in waters that plot in the immature water field in the Na–K–Mg diagram. The mixing trend between cold groundwaters from the recharge zone area (Zaccar Mount) and hot waters in the upflow area (Hammam Righa) is apparent via a chloride-enthalpy diagram that shows a mixing ratio of 22.6 < R < 29.2 %. We summarize these results with a geothermal conceptual model of the Hammam Righa geothermal field.     

Statistical and geochemical assessment of groundwater quality in Teboursouk area (Northwestern Tunisian Atlas)

Teboursouk region, Northwestern Tunisia, is characterized by the diversity of its natural resources (petroleum, groundwater and minerals). It constitutes a particular site widely studied, especially from a tectonic stand point as it exhibits a complex architecture dominated by multi-scale synclinals and Triassic extrusions. It has typical karst landform that constitutes important water resources devoted for human consumption and agriculture activities, besides to the exploitation of the Mio-Plio-Quaternary aquifer (MPQ). Thus, hydrogeological investigations play a significant role in the assessment of groundwater mineralization and the evaluation of the used water quality for different purposes. Hence, the current study based on a combined geochemical–statistical investigation of 50 groundwater samples from the multilayered aquifer system in the study area give crucial information about the principal factors and processes influencing groundwater chemistry. The chemical analysis of the water samples showed that Teboursouk groundwater is dominantly of Ca–Mg–Cl–SO₄ water type with little contribution of Ca–Mg–HCO₃, Na–K–Cl–SO₄ and Na–K–HCO₃. The total dissolved solids (TDS) values range from 0.37 to 3.58 g/l. The highest values are located near the Triassic outcrops. Furthermore, the hydrogeochemistry of the studied system was linked with various processes such as carbonates weathering, evaporites dissolution of Triassic outcrops and anthropogenic activities (nitrate contamination). Additionally, the main processes controlling Teboursouk water system were examined by means of multivariate statistical analysis (PCA and HCA) applied in this study based on 10 physicochemical parameters (TDS, pH, SO₄, HCO₃, pCO₂, Ca, Mg, Na, K, Cl and NO₃). Two principal components were extracted from PCA accounting 61% of total variance and revealing that the chemical characteristics of groundwater in the region were acquired through carbonates and evaporite dissolution besides to nitrate contamination. Similarly, according to Cluster analysis using Ward’s method and squared Euclidean distance, groundwater from the studied basin belongs to five different groups suggesting that the geochemical evolution of Teboursouk groundwater is controlled by dissolution of carbonates minerals, chemical weathering of Triassic evaporite outcrops, cation exchange and anthropogenic activities (nitrate contamination).     

Preliminary groundwater quality assessment in the central region of Ghana

Insufficient knowledge of the hydrogeochemistry of aquifers in the Central Region of Ghana has necessitated a preliminary water quality assessment in some parts of the region. Major and minor ions, and trace metal compositions of groundwater have been studied with the aim of evaluating hydrogeochemical processes that are likely to impair the quality of water in the study area. The results show that groundwater in the area is weakly acidic with mean acidity being 5.83 pH units. The dominant cation in the area is Na, followed by K, Ca, and Mg, and the dominant anion is Cl^?, followed by HCO₃ ^? and SO₄ ^2?. Two major hydrochemical facies have been identified as Na–Cl and Na–HCO_3, water types. Multivariate statistical techniques such as cluster analysis (CA) and factor analysis/principal component analysis (PCA), in R mode, were employed to examine the chemical compositions of groundwater and to identify factors that influenced each. Q-mode CA analysis resulted in two distinct water types as established by the hydrochemical facies. Cluster 1 waters contain predominantly Na–Cl. Cluster 2 waters contain Na–HCO₃ and Na–Cl. Cluster 2 waters are fresher and of good quality than cluster 1. Factor analysis yielded five significant factors, explaining 86.56% of the total variance. PC1 explains 41.95% of the variance and is contributed by temperature, electrical conductivity, TDS, turbidity, SO₄ ^2?, Cl^?, Na, K, Ca, Mg, and Mn and influenced by geochemical processes such as weathering, mineral dissolution, cation exchange, and oxidation–reduction reactions. PC2 explains 16.43% of the total variance and is characterized by high positive loadings of pH and HCO₃ ^?. This results from biogenic activities taking place to generate gaseous carbon dioxide that reacts with infiltrating water to generate HCO₃ ^?, which intend affect the pH. PC3 explains 11.17% of the total variance and is negatively loaded on PO₄ ^3? and NO₃ ^? indicating anthropogenic influence. The R-mode PCA, supported by R-mode CA, have revealed hydrogeochemical processes as the major sources of ions in the groundwater. Factor score plot revealed a possible flow direction from the northern sections of the study area, marked by higher topography, to the south. Compositional relations confirmed the predominant geochemical process responsible for the various ions in the groundwater as mineral dissolution and thus agree with the multivariate analysis.     

Geochemical patterns and origin of alkaline thermal waters in Central Greece (Platystomo and Smokovo areas)

This study investigates the origin and chemical composition of the thermal waters of Platystomo and Smokovo areas in Central Greece as well as any possible relationships of them to the neighboring geothermal fields located in the south-eastern part of Sperchios basin. The correlations between different dissolved salts and the temperature indicate that the chemical composition of thermal waters are controlled by, the mineral dissolution and the temperature, the reactions due to CO₂ that originates possibly by diffusion from the geothermal fields of Sperchios basin and the mixing of thermal waters with fresh groundwater from karst or shallow aquifers. Two major groups of waters are recognized on the basis of their chemistry: thermal waters of Na–HCO₃–Cl type and thermal waters mixed with fresh groundwater of Ca–Mg–Na–HCO₃ type. All thermal waters of the study area are considered as modified by water–rock interaction rainwater, heated in depth and mixed in some cases with fresh groundwater when arriving to the surface. Trace elements present low concentrations. Lithium content suggests discrimination between the above two groups of waters. Boron geochemistry confirms all the above remarks. Boron concentration ranges from 60 μg L^?1 to 10 mg L^?1, while all samples’ constant isotopic composition (δ¹¹B ≈ 10 ‰) indicates leaching from rocks. The positive correlation between the chemical elements and the temperature clearly indicates that much of the dissolved salts are derived from water–rock interactions. The application of geothermometers suggests that the reservoir temperature is around 100–110 °C. Chalcedony temperatures are similar to the emergent temperatures and this is typical of convective waters in fault systems in normal thermal gradient areas.     

Hydrogeochemical investigations of thermal waters in the northeastern part of Morocco

Northeastern Morocco is characterised by a large number of surface geothermal manifestations. Thermal waters are hosted within sedimentary rocks, and in particular the Liassic dolomitic limestones act as a reservoir. The presence of geothermal waters is closely related to important fault systems. Meteoric water infiltrates along those fractures and faults, gets heated, and then returns to the surface through hydrothermal conduits. Most of the thermal waters are of Na–Cl and Ca–Mg–HCO₃ types. In this paper different geochemical approaches were applied to infer the reservoir temperature. Na–K–Mg^1/2 ternary diagram points to temperatures ranging from 100 to 180 °C. Cation geothermometers suggest an average reservoir temperature of about 100 °C. Mineral solution equilibria analysis yields temperatures ranging from 50 to 185 °C. The silica enthalpy mixture model gives an average value (about 110 °C) higher than that inferred from cation geothermometers.     

Assessment of hydrogeochemistry and contamination of Varamin deep aquifer,Tehran Province,Iran

The present study investigates the hydrogeochemistry and contamination of Varamin deep aquifer located in the southeast of Tehran province, Iran. The study also evaluates groundwater suitability for irrigation uses. The hydrogeochemical study was conducted by collecting and analyzing 154 groundwater samples seasonally during 2014. Based on evolutionary sequence of Chebotarev, the aquifer is in the stage of SO₄ + HCO₃ in the north half of the plain and it has evolved into SO₄ + Cl in the south half. The unusual increase in TDS and Cl^? toward the western boundaries of the aquifer indicates some anomalies. These anomalies have originated from discharge of untreated wastewater of Tehran city in these areas. The studied aquifer contains four dominant groundwater types including Na–Ca–SO₄ (55%), Na–Ca–HCO₃ (22%), Na–Cl (13%) and Ca–Cl (10%). The spatial distributions of Na–Cl and Ca–Cl water types coincide with observed anomalies. Ionic relationships of SO₄ ^2? versus Cl^? and Na⁺ versus Cl^? confirm that water–rock interaction and anthropogenic contribution are main sources of these ions in the groundwater. The main processes governing the chemistry of the groundwater are the dissolution of calcite, dolomite and gypsum along the flow path, and direct ion exchange. Reverse ion exchange controls the groundwater chemistry in the areas contaminated with untreated wastewater. Based on Na% and SAR, 10.3 and 27% of water samples are unsuitable for irrigation purposes, respectively. Regarding residual sodium carbonate, there is no treat for crop yields. Only 6% of water samples represent magnesium adsorption ratios more than 50% which are harmful and unsuitable for irrigation.     

An appraisal of groundwater quality in Seymour and Blaine aquifers in a major agro-ecological region in Texas,USA

Aquifer-based groundwater quality assessment offers critical insight into the major hydrochemical processes, and aids in making groundwater resources management decisions. The Texas Rolling Plains (TRP), spanning over 22 counties, is a major agro-ecological region in Texas from where highest groundwater nitrate (NO₃ ^?) levels in the state have been reported. In this study, we present a comparative assessment of major hydrochemical facies pertaining to NO₃ ^? contamination and a host of species such as sulfate (SO₄ ^2?), chloride (Cl^?), and total dissolved solids (TDS) in different water use classes in the Seymour and Blaine aquifers, underlying the TRP. Aquifer-stratified groundwater quality information from 1990 to 2010 was obtained from the Texas Water Development Board and aggregated over decadal scale. High groundwater salinization was found in the municipal water use class in the Blaine aquifer with about 100, 87 and 50 % of observations exceeding the secondary maximum contaminant level for TDS, SO₄ ^2?, and Cl^?, respectively in the 2000s (2000–2010). The NO₃-contamination was more alarming in the Seymour aquifer with 82 and 61 % of observations, respectively, exceeding the maximum contaminant level (MCL) in the irrigation and municipal water use classes in the 2000s. Salinization was more influenced by SO₄ ^2? and Cl^? in the Blaine aquifer and by NO₃ ^? in the Seymour aquifer. High NO₃ ^? (>MCL) observations in the Seymour aquifer occurred in the Ca–HCO₃ and Ca–Mg–HCO₃ facies, the domains of fresh water recharge and anthropogenic influences (e.g., agricultural activities, waste disposal). High SO₄ ^2?, Cl^? and TDS observations in the Blaine aquifer dominated the Ca–Cl, Na–Cl, and mixed Ca(Mg)–SO₄(Cl) facies indicating evaporite dissolution, mixing and solute exchange, and lack of fresh recharge.     

A geochemical and stable isotope investigation of groundwater/surface-water interactions in the Velenje Basin,Slovenia

The geochemical and isotopic composition of surface waters and groundwater in the Velenje Basin, Slovenia, was investigated seasonally to determine the relationship between major aquifers and surface waters, water–rock reactions, relative ages of groundwater, and biogeochemical processes. Groundwater in the Triassic aquifer is dominated by HCO₃ ^–, Ca²⁺, Mg²⁺ and δ¹³C_DIC indicating degradation of soil organic matter and dissolution of carbonate minerals, similar to surface waters. In addition, groundwater in the Triassic aquifer has δ¹⁸O and δD values that plot near surface waters on the local and global meteoric water lines, and detectable tritium, likely reflecting recent (<50 years) recharge. In contrast, groundwater in the Pliocene aquifers is enriched in Mg²⁺, Na⁺, Ca²⁺, K⁺, and Si, and has high alkalinity and δ¹³C_DIC values, with low SO₄ ^2– and NO₃ ^– concentrations. These waters have likely been influenced by sulfate reduction and microbial methanogenesis associated with coal seams and dissolution of feldspars and Mg-rich clay minerals. Pliocene aquifer waters are also depleted in ¹⁸O and ²H, and have ³H concentrations near the detection limit, suggesting these waters are older, had a different recharge source, and have not mixed extensively with groundwater in the Triassic aquifer.     

Hydrogeochemical assessment of groundwater quality along the coastal aquifers of southern Tamil Nadu,India

Hydrogeochemical investigation of groundwater has been carried out in the coastal aquifers of southern Tamil Nadu, India. Seventy-nine dug well samples were collected and analyzed for various physicochemical parameters. The result of the geochemical analysis indicates the groundwater in the study area is slightly alkaline with moderate saline water. The cation and anion concentrations confirm most of the groundwater samples belong to the order of Na⁺ > Mg²⁺ > Ca²⁺ > K⁺ and Cl^? > SO₄ ^2? > HCO₃ ^?. Thereby three major hydrochemical facies (Ca–Cl, mixed Ca–Mg–Cl and Na–Cl) were identified. Based on the US Salinity diagram, majority of the samples fall under medium to very high salinity with low to high sodium hazard. The cross plot of Ca²⁺ + Mg²⁺ versus chloride shows 61 % of the samples fall under saline water category. Higher EC, TDS and Cl concentrations were observed from Tiruchendur to Koodankulam coastal zone. It indicates that these regions are significantly affected by saltwater contamination due to seawater intrusion, saltpan deposits, and beach placer mining activities.     

A hydrogeochemical approach to evaluate the occurrence and source of salinization in the shallow aquifers of the southeastern Imphal valley in the Indo-Myanmar range of Northeast India

The Imphal valley is an intramontane basin confined within an anticlinorium of several anticlines and synclines in the Disang Group of rocks of Tertiary age. This valley of more than 2 million people is occupied by fluvio-lacustrine deposits of Quaternary age and is located in the central part of the Indo-Myanmar range of Northeast India. The hydrogeochemical parameters of temperature, pH, ORP, TDS, Na, Cl, Br, Ba, B, Sr, Li, δ¹⁸O, HCO₃, K, Mg, Ca, NO₃, PO₄, SO₄ in 173 samples using ion-chromatograph, ICP (AES), ICP (OES), ICP (MS) and 37 dugwells were studied to understand the occurrence and origin of salinization process for the first time. The order of abundance of ions is identified as HCO₃ > Na > Cl > Ca > Mg > K > NO₃ > PO₄ > Sr > Br > B>Ba > Li > SO₄. Five hydrochemical facies (Na–Cl, Ca–Mg–HCO₃, Na–HCO₃, Ca–Mg–HCO₃–Cl and Ca–Mg–Cl) represent the types of waters. The saline-dominated water types (Na–Cl and Na–HCO₃) represent piedmont and the rest of the facies represent alluvial plain and flood plain groundwaters. Durov’s diagram reveales initial and intermediate stages of groundwater evolution. Isotope δ¹⁸O, Gibbs diagram and ions scatter plots suggest evaporation and crystallization processes leading to halite encrustation in the Disang shales. Negative Eh, low NO₃ and the absence of SO₄ indicates reduced condition coupled with rich dissolve organic matters leading to elevation of salts in soils around piedmont where the rock type is exclusively of the Disang shales. Trilinear plot, correlation matrix and water table flow analysis suggest salinization of groundwater originates in piedmont groundwater and disseminates towards alluvial plain and flood plain along the flow path.     

Groundwater recharge,circulation and geochemical evolution in the source region of the Blue Nile River,Ethiopia

Geochemical and environmental isotope data were used to gain the first regional picture of groundwater recharge, circulation and its hydrochemical evolution in the upper Blue Nile River basin of Ethiopia. Q-mode statistical cluster analysis (HCA) was used to classify water into objective groups and to conduct inverse geochemical modeling among the groups. Two major structurally deformed regions with distinct groundwater circulation and evolution history were identified. These are the Lake Tana Graben (LTG) and the Yerer Tullu Wellel Volcanic Lineament Zone (YTVL). Silicate hydrolysis accompanied by CO₂ influx from deeper sources plays a major role in groundwater chemical evolution of the high TDS Na–HCO₃ type thermal groundwaters of these two regions. In the basaltic plateau outside these two zones, groundwater recharge takes place rapidly through fractured basalts, groundwater flow paths are short and they are characterized by low TDS and are Ca–Mg–HCO₃ type waters. Despite the high altitude (mean altitude ∼2500 masl) and the relatively low mean annual air temperature (18 °C) of the region compared to Sahelian Africa, there is no commensurate depletion in δ¹⁸O compositions of groundwaters of the Ethiopian Plateau. Generally the highland areas north and east of the basin are characterized by relatively depleted δ¹⁸O groundwaters. Altitudinal depletion of δ¹⁸O is 0.1‰/100 m. The meteoric waters of the Blue Nile River basin have higher d-excess compared to the meteoric waters of the Ethiopian Rift and that of its White Nile sister basin which emerges from the equatorial lakes region. The geochemically evolved groundwaters of the YTVL and LTG are relatively isotopically depleted when compared to the present day meteoric waters reflecting recharge under colder climate and their high altitude.     

Geochemistry of Thermal Waters of Continental Margin of Far East of Russia

Studied waters belong to warm(T=30-50℃),alkaline(pH=8.9-9.3),low mineralized(TDS235 mg/1)Na-HCO_3 or Na-SO_4-HCO_3 thermal waters with high content of SiO_2(up to 81 mg/l)and F(up to 3.9 mg/1),occur on modern volcano-tectonic rejuvenated areas of Eastern Sikhote-Alin orogenic belt.Low~3He concentration as well as N_2/O_2 and N_2/Ar ratios exclude influence of deep mantle fluid.New rare earth element data constrain our understandmg of water-rock interaction occurring in the water source region.Meteoric origin of waters is proved by stable isotope values varying from-71‰to-136.1‰and from-10.8‰to-18.8‰forδ~2U andδ~(18)O respectively.REE patterns reflect high pH,resultfing from water-rock interaction and oxidative conditions.Calculations of deep aquifer temperature using Na-K and quartz geothermometers show 116.8-131.1°C and 82.2-125.8℃respectively.Presence of deep faults both with abnormal thermal gradient(~45-50 K/km)define unique geochemical shape of thermal waters of Sikhote-Alin,area,where no present volcanic activity is registered.     

Chemical evolution of thermal waters from limestone aquifers of the Southern Upper Rhine Valley

Thermal spas in the Upper Rhine Graben recover their waters mainly from two different limestone aquifers, Hauptrogenstein (Middle Jurassic) and Muschelkalk (Middle Triassic). The thermal waters are heated along anomalous high thermal gradients in the Tertiary rift valley. The highest well head temperature is about 40°C in Hauptrogenstein wells and 60°C in Muschelkalk wells. Mineralization (TDS) is up to 5 g/kg in Hauptrogenstein and as high as 17 g/kg in the Muschelkalk aquifer. About 300 chemical analyses from 13 wells were used in this study.Compositional relationships between major chemical components (Na/Cl, K/Cl, Mg/Cl, SO₄/Cl, Cl/Br and Na/Br) suggest that thermal water from the Hauptrogenstein originates from mixing of 3 components: (a) meteoric water, (b) fossil seawater (residual formation water) and (c) a third component that resulted from water–rock reaction.The total amount of dissolved solids and the water type from the deeper Muschelkalk aquifer depends on the depth of the aquifer at the well location. The chemical characteristics of the thermal water indicate that water composition is derived mainly from water–rock interaction.     

Hydrochemical characterization and groundwater quality in Delta Tokar alluvial plain, Red Sea coast—Sudan

The leaching processes along the flow path and over abstraction of the alluvial aquifer, the principal aquifer in delta Tokar, by the agricultural and domestic sectors and natural factors, have led to its salinization which may be due to interaction between geological formations and adjacent brackish and saline water bodies as well as seawater transgression. The main objectives of this study are to assess the hydrochemical characteristics of the groundwater and to delineate the locations and the sources of aquifer salinization. Water samples in the project area were chemically analyzed for major cations and anions at the laboratory by the standard analytical procedures. Chemical data and water level measurements were manipulated using GIS techniques for hydro chemical and flow direction maps and piper diagram for chemical facies and SPSS software for statistical analyses such as basic statistics (mean and standard deviation) and Spearman’s correlation matrix. The general flow direction of the groundwater is from Southwest towards East and Northeast. The hydraulic gradient is relatively steeper at the apex of the delta (0.06) and amounts to 0.005 at the distal part of the delta. The average transmissivity value of the water bearing formations was found to be about 4.5?×?10³ m²/s, whereas, the storage coefficient was about 0.28. A hydrochemical study identified the locations and the sources of aquifer salinization and delineated their areas of influence. The investigation indicates that the aquifer water quality is significantly modified as groundwater flows from the southwestern parts of the study area, where the aquifer receives its water by lateral underflow from Khor Baraka flood plain, to the central and northeastern parts, with few exceptions of scattered anomalous concentration pockets in the deltaic plain. Significant correlation between TDS and/or EC with the major components of Na⁺, Cl^?, and SO ₄ ^?2 ions is an indication of seawater influence on the groundwater salinity. Moreover, Cl^?, SO ₄ ^2? , and Na⁺ are predominant ions followed by Ca²⁺ and HCO ₃ ^? . Hence, four types of groundwater can be chemically distinguished: Na–Ca–SO₄–Cl– facies, Na–Cl–SO₄–HCO₃– facies, Na–Ca–Mg–SO₄–Cl–HCO₃ facies, and Na–Ca–Mg–Cl–SO₄ facies. The processes that govern changes in groundwater composition as revealed by chemical and statistical analyses are mainly associated with over-abstraction, biodegradation, marine intrusions, and carbonate saturation.     

Hydrochemistry of groundwater and its assessment for irrigation purpose in coastal Jeffara Aquifer, southeastern Tunisia

Groundwater is of a paramount importance in arid areas, as it represents the main water resource to satisfy the different needs of the various sectors. Nevertheless, coastal aquifers are generally subjected to seawater intrusion and groundwater quality degradation. In this study, the groundwater quality of the coastal Jeffara aquifer (southeastern Tunisia) is evaluated to check its suitability for irrigation purposes. A total of 74 groundwater samples were collected and analyzed for various physical and chemical parameters, such as, electrical conductivity, pH, dissolved solids (TDS), Na, K, Ca, Mg, Cl, HCO₃, and SO₄. Sodium adsorption ratio, magnesium adsorption ratio, Sodium percentage, and permeability index were calculated based on the analytical results. The analytical results obtained show a strong mineralization of the water in the studied aquifer. TDS concentrations range from 3.40 to 18.84 g?L^?1. Groundwater salinity was shown to be mainly controlled by sodium and chloride. The dominant hydrochemical facieses are Na–Cl–Ca–SO₄, mainly as a result of mineral dissolution (halite and gypsum), infiltration of saline surface water, and seawater intrusion. Assessment of the groundwater quality of the different samples by various methods indicated that only 7% of the water, in the northwest of the study area, is considered suitable for irrigation purposes while 93% are characterized by fair to poor quality, and are therefore just suitable or unsuitable for irrigation purposes.     

Quantification of groundwater–seawater interaction in a coastal sandy aquifer system: a study from Panama,Sri Lanka

The Panama coastal aquifer system is an important water resource in the southeast coast of Sri Lanka that provides adequate supplies of water for agriculture and domestic uses. One of the biggest threats to these fragile aquifers is the sea water intrusion. In this study, recharging mechanism and geochemical evaluation of groundwater in the coastal sandy aquifer of Panama were evaluated using chemical and stable isotope techniques. Thirty groundwater samples were collected and analyzed for their major ion concentrations and stable isotope ratios of oxygen (¹⁸O/¹⁶O) and hydrogen (D/H). All studied samples showed a ranking of major anions in the order Cl^? > HCO ₃ ^?  > SO ₄ ^2?  > N-NO₃ ^? while cations showed a decreasing order of abundance with Na⁺ > Ca²⁺ > Mg²⁺ > K⁺. Dominant groundwater hydrogeochemical types were Na–Cl and mixed Ca–Mg–Cl. Results of saturation index calculations indicate that the investigated groundwater body was mostly saturated with respect to calcite, dolomite and gypsum. In addition, stable isotope and geochemical data suggest that fresh groundwater in the aquifer is recharged mainly by local precipitation with slight modification from evaporation and saline water intrusions. Isotope data suggest that mixing of salt water with freshwater occurs in aquifers which are located towards the lagoon. Since the communities in the study area depend entirely on groundwater, an understanding of the hydrogeochemical characteristics of the aquifer system is extremely important for the better water resource management in the region.     

A geochemical and 3D-geometry geophysical survey to assess artificial groundwater recharge potential in the Pacific coast of Baja California,Mexico

A geophysical and geochemical study was carried out in the Maneadero aquifer, Baja California, Mexico, with the aim of identifying potential recharge locations for reclaimed water (RW). This coastal aquifer shows a significant decline in water quality, both as a result of salinization and the pollution by nitrates. Total dissolved solids (TDS) in an extreme case increased from 4 g l^?1 in 2000 to 27 g l^?1 in 2011. Nitrate as N–NO₃, reaches 46 mg l^?1. Based on their geochemistry and location, four water-quality zones are identified: (a) fresh water with TDS ≈ 1 g l^?1 in the upper creeks, (b) mixture between seawater and freshwater in the coast-proximal sections, (c) water significantly enriched in nitrate below and adjacent to the town of Maneadero, and (d) brackish water with no signs of current interaction with freshwater. The 3D geophysics identifies the influence of modern recharge areas and also buried flow-paths down to at least 30 m depth. The locations best suitable for aquifer recharge are those with equal or higher TDS concentrations (>2.5 g l^?1) than RW, which are located at the brackish water zone and/or at the coastal limits of the mixing zones.     

Morphology and growth of aragonite crystals in hot-spring travertines at Lake Bogoria, Kenya Rift Valley

Pseudohexagonal aragonite crystals are common components in some hot-spring travertines at Chemurkeu on the western shore of Lake Bogoria, Kenya. Beds, lenses and pods of aragonite crystals are intercalated with beds of white non-crystallographic calcite dendrites. The pseudohexagonal aragonite crystals, which are up to 4 cm long and 4 mm wide, are formed of nested skeletal crystals. Each skeletal crystal is formed of cyclical twinned crystals that are constructed of stacked subcrystals. The latter are inclined at a consistent angle of 40° to the long axis of the pseudohexagonal aragonite crystal. Intense competition for space during growth modified the crystal morphology with the result that many of the pseudohexagonal crystals are distorted. Intercrystalline and intracrystalline pores are filled or partly filled by epitaxial aragonite overgrowths and/or reticulate microbial coatings that have a high concentration of Si and Mg. In places, this extracellular mucus induced etching of the underlying aragonite crystal. Today the hot (T>95 °C) Na-HCO₃-Cl spring waters at Chemurkeu have a salinity of 5–6 g L^?1 TDS, a pH of 8·1–9·1, Ca²⁺ concentrations of <2 mg L^?1 and Mg²⁺ concentrations of <0·7 mg L^?1, The springs of the Lake Bogoria Geothermal Field are fed by a shallow aquifer (T～100 °C) and a deeper aquifer (T～170 °C). Springs at Chemurkeu derive from meteoric groundwater, lake water and condensed steam, and are fed mainly from the shallow thermal aquifer. Much of the aragonite may have formed when the spring waters contained more dissolved Ca²⁺ than today, possibly under more humid conditions during the Holocene.     

Carbonate weathering and connate seawater influencing karst groundwaters in the Gevas–Gurpinar–Güzelsu basins,Turkey

There are 59 springs at the Gevas–Gurp?nar–Güzelsu basins, 38 of these springs emerge from the fractured karst aquifers (recrystallized limestone and travertine) and 21 emerge from the Yuksekova ophiolites, K?rkgeçit formation and alluvium. The groundwater samples collected from 38 out of the total of 59 springs, two streams, one lake and 12 wells were analyzed physico-chemically in the year 2002. EC and TDS values of groundwater increased from the marble (high altitude) to the ophiolites and alluvium (toward Lake Van) as a result of carbonate dissolution and connate seawater. Five chemical types of groundwater are identified: Ca–Mg–HCO₃, Mg–Ca–HCO₃, Mg–Na–HCO₃, Na–Ca–HCO₃ and Mg–Ca–Na–HCO₃. The calculations and hydrochemical interpretations show that the high concentrations of Ca²⁺, Mg²⁺ and HCO₃ ^? as predominant ions in the waters are mainly attributed to carbonate rocks and high pCO₂ in soil. Most of the karst springs are oversaturated in calcite, aragonite and dolomite and undersaturated in gypsum, halite and anhydrite. The water–rock interaction processes that singly or in combination influence the chemical composition of each water type include dissolution of carbonate (calcite and dolomite), calcite precipitation, cation exchange and freshening of connate seawater. These processes contribute considerably to the concentration of major ions in the groundwater. Stable isotope contents of the groundwater suggest mainly direct integrative recharge.