Hydrogeochemistry of groundwaters in a semi-arid region. El Ma El Abiod aquifer, Eastern Algeria

In this work, we present results of the hydrogeochemical and isotopic studies on groundwater samples from the El Ma El Abiod Sandstone aquifer, in Tébessa, Algeria. Chemical and environmental isotope data are presented and discussed in order to identify the geochemical processes and their relation with groundwater quality as well as to get an insight into the hydrochemical evaluation, in space and time, of groundwater and of the origin of dissolved species. A combined hydrogeologic and isotopic investigation have been carried out using chemical and isotopic data to deduce a hydrochemical evaluation of the aquifer system based on the ionic constituents, water types, hydrochemical facies, and factors controlling groundwater quality. All of the investigated groundwaters are categorized into two chemical types: low mineralized water type and relatively high mineralized water type. Interpretation of chemical data, based on thermodynamic calculations and geochemical reaction models of selected water groups constructed using PHREEQC, suggest that the chemical evolution of groundwater is primarily controlled by water–rock interactions, involving (1) acidic weathering of aluminosilicates, (2) dissolution of secondary carbonate minerals, and (3) cation exchange of Na⁺ for Ca²⁺. However, the original composition of groundwater may have been modified by further secondary processes such as mixing of chemically different water masses. The combined use of SI and mass-balance modeling has shown to be a useful approach in interpreting groundwater hydrochemistry in an area where large uncertainties exist in the understanding of the groundwater flow system. Interpretation of ¹⁸O and ²H, suggest that the recharge of the investigated groundwaters may result from different mechanisms.     

Recharge mode and mineralization of groundwater in a semi-arid region: Sidi Bouzid plain (central Tunisia)

Groundwater is the most important source of water supply in Sidi Bouzid plain located in central Tunisia. Proper understanding of the geochemical evolution of groundwater is important for sustainable development of water resources in this region. A hydrogeochemical survey was conducted on the Mio–Plio–Quaternary aquifer system using stable isotopes, radiocarbon, tritium and major elements, in order to evaluate the groundwater chemistry patterns and the main mineralization processes occurring in this system. The chemical data indicate that dissolution of evaporate minerals and evaporation are the main processes controlling groundwater mineralization. The isotopic data show that groundwater in the study area is a mixture of recent shallow waters located upstream and along Wadi Al Fakka bed and paleowaters located towards plain limits and discharge areas. Low ³H and ¹⁴C contents are observed in major part of the plain indicating that recharge of the aquifer occurs mainly through direct infiltration at Wadi Al Fakka while there is no evidence of significant recharge in major part of the plain and mountains piedmonts.     

Using 87Sr/86Sr, δ18O and δ2H isotopes along with major chemical composition to assess groundwater salinization in lower Shire valley,Malawi

Groundwater resources in some parts of the lower section of Shire River valley, Malawi, are not useable for rural domestic water supply due to high salinity. In this study, a combined assessment of isotopic (⁸⁷Sr/⁸⁶Sr, δ¹⁸O and δ²H) and major ion composition was conducted in order to identify the hydro-geochemical evolution of the groundwater and thereby the causes of salinity. Three major end-members (representing fresh- and saline groundwater, and evaporated recharge) were identified based on major ion and isotopic composition. The saline groundwater is inferred to result from dissolution of evaporitic salts (halite) and the fresh groundwater shows influence of silicate weathering. Conservative mixing models show that brackish groundwater samples result from a three component mixture comprising the identified end-members. Hence their salinity is interpreted to result from mixing of fresh groundwater with evaporated recharge and saline groundwater. On the other hand, the groundwater with low TDS, found at some distance from areas of high salinity, is influenced by mixing of evaporated recharge and fresh groundwater only. Close to the Shire marshes, where there is shallow groundwater, composition of stable isotopes of water indicates that evaporation may also be an important factor.     

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.     

Geochemical and isotopic characterization of groundwater from shallow and deep limestone aquifers system of Aleppo basin (north Syria)

Stable isotopes (δ¹⁸O, δ²H and ¹³C) and radioactivity (³H, ¹⁴C) have been used in conjunction with chemical data to evaluate the processes generating the chemical composition, reconstruct the origin of the water and groundwater residence time. The Aleppo basin is comprised of two main limestone aquifers: the first one is unconfined of Paleogene age and the second is confined of Upper Cretaceous age. The chemical data indicate that the dissolution of minerals and evaporation are the main processes controlling groundwater mineralization. The groundwater from the two aquifers is characterized by distinctive stable isotope signatures. This difference in water isotopes is interpreted in terms of difference origin and recharge period. Fresh and brackish shallow groundwater were mostly recharged during the Holocene period. The presence of ³H in several groundwater samples of this aquifer gives evidence that groundwater recharge is going on. Brackish water of the deep confined aquifer has depleted stable isotope composition and very low ¹⁴C activity that indicates recharge during the late Pleistocene cold period.     

Hydrogeochemistry and isotope techniques to determine water interactions in groundwater-dependent shallow lakes,Wet Pampa Plain,Argentina

This paper gives an account of the implementation of hydrochemical and isotopic techniques to identify and explain the processes that govern solute exchange in two groundwater-dependent shallow lakes in the Southeastern Pampa Plain of Argentina. Water samples (lakes, streams, spring water and groundwater) for hydrochemical and stable isotopic determination were collected and the main physical–chemical parameters were measured. The combination of stable isotope data with hydrogeochemical techniques was used for the identification of sources and preferential recharge areas to these aquatic ecosystems which allowed the explanation of the lake water origin. The hydrochemical processes which explain Los Padres Lake water chemistry are evaporation from groundwater, CO₂ input, calcite dissolution, Na⁺ release by Ca²⁺ and Mg²⁺ exchange, and sulfate reduction. The model that best aligns with La Brava Lake hydrochemical constraints includes: mixing, CO₂ and calcite dissolution, cationic exchange with Na⁺ release and Mg²⁺ adsorption, and to a lesser extent, Ca/Na exchange. This model suggests that the fractured aquifer contribution to this water body is greater than 50 %. An isotopic-specific fingerprint for each lake was identified, finding a higher evaporation rate for La Brava Lake compared to Los Padres Lake. Isotopic data demonstrate the importance of these shallow lakes as recharge areas to the regional aquifer, becoming areas of high groundwater vulnerability. The Tandilia Range System, considered in many hydrogeological studies as the impermeable bedrock of the Pampean aquifer, acts as a fissured aquifer in this area, contributing to low salinity waters and with a fingerprint similar to groundwater isotopic composition.     

Groundwater flow and residence time in a karst aquifer using ion and isotope characterization

In order to identify the origin of the main processes that affect the composition of groundwater in a karstic aquifer, a hydrogeochemical and isotopic study was carried out of water from numerous observation wells located in Sierra de Gador, a semiarid region in SE Spain. Several natural and anthropogenic tracers were used to calculate groundwater residence time within this complex aquifer system. Analysis of major ions enabled the principal geochemical processes occurring in the aquifer to be established, and the samples were classified into four distinctive solute groups according to this criterion. Dissolution of carbonate rocks determines the chemical composition of less mineralized water. In another group, the concurrent dissolution of dolomite and precipitation of calcite in gypsum-bearing carbonate aquifer, where the dissolution of relatively soluble gypsum controls the reaction, are the dominant processes. Marine intrusion results in highly mineralized waters and leads to base exchange reactions. The groundwater enrichment of minor and trace elements allowed classification of the samples into two classes that are linked to different flow patterns. One of these classes is influenced by a slow and/or deep regional flow, where the temperature is generally elevated. The influence of sulphate reduces by up to 40 % the barium concentration due to the barite precipitation. Isotope data (T, ¹⁴C) confirm the existence of recent local flows, and regional flow system, and ages of ground water may reach 8000 years. The importance of gypsum dissolution in this aquifer is proved by the δ³⁴S content.     

Hydrochemical characterization of groundwater in the Accra plains of Ghana

Chemical and isotopic analyses are used to characterize and identify the relevant water-rock interactions, which are responsible for the poor groundwater quality in the Accra Plains. Four main water types are identified. Processes that singly or in combination influence the chemical composition of each water type include halite dissolution carbonate dissolution and precipitation, seawater intrusion, cation exchange, evaporative concentration of solutes and aluminosilicates dissolution. These processes contribute considerably to the concentration of major ions in the groundwater. Stable isotope contents of the groundwater suggest mainly direct integrative recharge. A few samples plot along the meteoric-seawater mix line which is coincidentally the evaporative line. The Cl⁻/Br⁻ ratios of some of these are close to 300 confirming marine origin, others probably concentrated by evaporation have their Cl⁻/Br⁻ ratios significantly lower than 300. Groundwater is qualitatively good for drinking purposes only along the foothills of the Akwapim Togoland ranges.     

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.     

Hydrogeochemistry of the Saloum (Senegal) superficial coastal aquifer

Seawater has entered and concentrated in the Saloum hydrologic system up to 100 km upstream, contaminating both the surface water and the superficial 'Continental terminal' (CT) groundwater resources, and large proportions of cultivated lands. In the areas affected by saltwater contamination, chloride concentrations as high as 3,195 mg/l have been measured in the groundwater samples collected from wells located in the vicinity of the Saloum River, making the water inadequate for drinking water purposes. This paper presents the results of a study designed to characterise the current extent of the saline groundwater and the mechanism of saline surface water body/fresh groundwater mixing in relation to the groundwater flow trends. It also describes the groundwater chemical and isotopic composition and geochemical processes controlling the chemical patterns. Four major water types occur in the study area, namely Na-rich saline groundwater, Ca-Na-rich saline groundwater, Na-dominant fresh groundwater and Ca-dominant fresh groundwater. A hydrogeochemical zonation of the aquifer, based on the presence of different water families and on the groundwater flow, led to the identification of the main processes controlling the groundwater chemistry. Cation exchange reactions on the kaolinite clay mineral, calcite dissolution in the eastern zone where calcite minerals have been identified, reverse cation exchange reactions in the saline-contaminated band along the Saloum River and, to a lesser extent, a gypsum dissolution are the predominant processes. Results of i¹⁸O and iD analysis in 15 groundwater samples compared with the local meteoric line indicate that the groundwater has been affected by evaporation, and the groundwater is isotopically lighter as the depth of water table increases. In this study, i¹⁸O data were used in conjunction with chloride data to identify the source of high chloride. Results show a departure of the contaminated water samples from the seawater mixing line, which indicates that other processes rather than mixing between modern seawater and native groundwater alone increase the chloride concentrations.     

Genesis of the mineral groundwaters of the Razdol’nenskii occurrence in Primorye

Original isotopic and chemical data are reported on the groundwater and gases from the unique occurrence of mineral water in the coastal zone of southern Primorye. Results of the δ¹⁸O and δ²H analysis of the underground and surface water of the area integrated with their δ¹³C composition made it possible to solve the problem of the genesis and evolution of groundwater and gases in the coastal part of the Sea of Japan. It was established that meteoric waters penetrate into the Mesozoic terrigenous rocks and changed their chemical composition under the influence of transformation of organic matter from the host rocks. CO₂ released owing to reactions provides multiple enrichment of the water in HCO₃ and stimulates Na influx via dissolution of aluminosilicates.     

Tracing salinization processes in coastal aquifers using an isotopic and geochemical approach: comparative studies in western Morocco and southwest Portugal

Environmental stable and radioactive isotopes (δ²H, δ¹³C, δ¹⁸O; ³H and ¹⁴C), together with physical and geochemical data, were used in the determination of the origins of groundwater salinization and geochemical evolution processes in coastal regions. Two case studies on the Atlantic Coast are discussed, one located in the Essaouira sedimentary basin, western Morocco, and the second, in the Lower Tagus–Sado sedimentary basin, southwest Portugal. In both regions, groundwater degradation occurs by salinization increase to different concentrations and in relation to different origins. The main quality issues for the groundwater resources are related to seawater intrusion, dissolution of diapiric structures intruding the aquifer layers, brine dissolution at depth, and/or evaporation of irrigation water. Anthropogenic pollution ascribed to agricultural activities is another source for groundwater degradation, affecting mainly the shallow aquifers. The apparent ¹⁴C age of the analysed samples ranges from 2.9?±?0.3 up to 45.6?±?0.6 pmC in the Miocene groundwater samples from the basin in Portugal; at the Essaouira basin in Morocco, the ¹⁴C content varies from 60 to 86 pmC. In most of the water samples, the ³H concentration is below the detection limit. In both basins, the isotopic results together with the geochemical data provided an effective label for tracing the mineralization origin and groundwater degradation processes. Further, the isotopic signatures were used in the identification of a paleoclimate (colder period), recorded in the stable isotopic composition and corroborated with the ¹⁴C data.     

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.     

Delineation of groundwater provenance in a coastal aquifer using statistical and isotopic methods,Southeast Tanzania

Rapid population growth and urbanization has placed a high demand on freshwater resources in southeast costal Tanzania. In this paper, we identify the various sources of groundwater and the major factors affecting the groundwater quality by means of multivariate statistical analyses, using chemical tracers and stable isotope signatures. The results from hierarchical cluster analyses show that the groundwater in the study area may be classified into four groups. A factor analysis indicates that groundwater composition is mainly affected by three processes, accounting for 80.6% of the total data variance: seawater intrusion, dilution of groundwater by recharge, and sewage infiltration. The hydrochemical facies of shallow groundwater was mostly of the Na–Ca–Cl type, although other water types were also observed. The deep groundwater samples were slightly to moderately mineralized and they were of the NaHCO₃ type. This water type is induced mainly by dissolution of carbonate minerals and modified by ion exchange reactions. The signal from the stable isotope composition of the groundwater samples corresponded well with the major chemical characteristics. In the shallow groundwater, both high-nitrate and high-chloride concentrations were associated with localized stable isotope enrichments which offset the meteoric isotopic signature. This is inferred to be due to the contamination by influx of sewage, as well as intrusion by seawater. The depleted stable isotope values, which coincides with a chemical signature for the deep aquifer indicates that this deep groundwater is derived from infiltration in the recharge zone followed by slow lateral percolation. This study shows that a conceptual hydrogeochemical interpretation of the results from multivariate statistical analysis (using HCA and FA) on water chemistry, including isotopic data, provides a powerful tool for classifying the sources of groundwater and identifying the significant factors governing the groundwater quality. The derived knowledge generated by this study constitutes a conceptual framework for investigating groundwater characteristics. This is a prerequisite for developing a sound management plan, which is a requirement for ensuring a sustainable exploitation of the deep aquifer water resource in the coastal area of Tanzania.     

Hydrogeological and hydrochemical investigation of groundwater using environmental isotopes (18O, 2H, 3H, 14C) and chemical tracers: a case study of the intermediate aquifer,Sfax, southeastern Tunisia

Major element concentrations and stable (δ¹⁸O and δ²H) and radiogenic (³H and ¹⁴C) isotopes in groundwater have proved useful tracers for understanding the geochemical processes that control groundwater mineralization and for identifying recharge sources in the semi-arid region of Sfax (southeastern Tunisia). Major-ion chemical data indicate that the origins of the salinity in the groundwater are the water–rock interactions, mainly the dissolution of evaporitic minerals, as well as the cation exchange with clay minerals. The δ¹⁸O and δ²H relationships suggest variations in groundwater recharge mechanisms. Strong evaporation during recharge with limited rapid water infiltration is evident in the groundwater of the intermediate aquifer. The mixing with old groundwater in some areas explains the low stable isotope values of some groundwater samples. Groundwaters from the intermediate aquifer are classified into two main water types: Ca-Na-SO₄ and Ca-Na-Cl-SO₄. The high nitrate concentrations suggest an anthropogenic source of nitrogen contamination caused by intensive agricultural activities in the area. The stable isotopic signatures reveal three water groups: non-evaporated waters that indicate recharge by recent infiltrated water; evaporated waters that are characterized by relatively enriched δ¹⁸O and δ²H contents; and mixed groundwater (old/recent) or ancient groundwater, characterized by their depleted isotopic composition. Tritium data support the existence of recent limited recharge; however, other low tritium values are indicative of pre-nuclear recharge and/or mixing between pre-nuclear and contemporaneous recharge. The carbon-14 activities indicate that the groundwaters were mostly recharged under different climatic conditions during the cooler periods of the late Pleistocene and Holocene.

     

Isotopic and noble gas study of Chalk groundwater in the London Basin, England

The chemical and isotopic composition of groundwater from 52 sites in the London (U.K.) area was determined as part of a project aimed at assessing the spatial variation in the age of Chalk groundwater, and in determining the relationship between fracture and matrix groundwater in this dual porosity system.Systematic changes in groundwater chemistry take place in the downgradient direction in response to several chemical processes. These processes include early concentration by evaporation and congruent dissolution of calcite followed by widespread incongruent dissolution and ion exchange in addition to local oxidation-reduction reactions, gypsum dissolution and saline intrusion. As a result of the above processes, Chalk groundwater follows an evolutionary path from Ca bicarbonate type to Na bicarbonate type.The age of Chalk groundwater was modelled using¹⁴C, δ¹³C,³H, δ²H and δ¹⁸0. There is a general increase in the groundwater age in a downgradient direction with the oldest water found in N central areas of the basin. Groundwater in the unconfined zones and in areas S of the Greenwich fault is almost entirely of unevolved, modem composition. Carbon-14 modelling suggests that Chalk groundwater in the S basin is generally less than 10000 a old while that in the north is generally between 10000 and 25000 a old. The presence of³H in concentrations of up to 7 TU in groundwater which yields ages of several 1000 a, however, indicates that mechanisms exist for the rapid introduction of recent groundwater to the confined aquifer. Results of palaeorecharge temperature determinations using δ²H, δ¹⁸0 and noble gas analytical results suggest that significant Devensian recharge did indeed occur in the aquifer.A model of the development of the Chalk recognizes that it is a classic dual porosity aquifer in which groundwater flow occurs predominantly in the fracture system. The upper 50 m of the aquifer was flushed with fresh water during the 2–3 × 10⁶ a of the Quaternary and therefore meteoric water largely replaced the Tertiary and Cretaceous marine water that previously saturated the system. Most processes which control the chemistry of the groundwater occur in the matrix where the surface area is exceptionally high. Although fracture flow dominates the flow regime, diffusion from the matrix into the fracture porosity controls the chemistry of Chalk groundwater.     

Factors controlling mechanisms of groundwater salinization and hydrogeochemical processes in the Quaternary aquifer of the Eastern Nile Delta, Egypt

In this study, combining interpretations of conservative dissolved ions and environmental isotopes in water were used to investigate the main factors and mechanisms controlling groundwater salinization and hydrogeochemical processes in the Eastern Nile Delta, Egypt. Hydrogeochemical and isotopic study has been carried out for 61 water samples from the study area. Total dissolved solid (TDS) contents of groundwater are highly variable rising along flowpath from the south (410 mg/L) to the north (14,784 mg/L), implying significant deterioration and salinization of groundwater. Based on TDS and ionic ratios, groundwater samples were classified into three groups. In low-saline groups, water chemistry is greatly influenced by cation exchange, mineral dissolution/precipitation, anthropogenic pollutants and mixing with surface water. Whilst, in high-saline groups, water chemistry is affected by salt-water intrusion, reverse cation exchange and evaporation. The chemical constituents originating from saline water sources, reverse ion exchange and mineral dissolution are successfully differentiated using ionic delta and saturation index approaches. The δ¹⁸O–δ²H relationship plots on a typical evaporation line, suggesting potential evaporation of the recharging water prior to infiltration. Isotope evidence concludes that the groundwater have been considerably formed by mixing between depleted meteoric water recharged under different climatic conditions and recently infiltrating enriched surface water and excess of irrigation water. The δ¹⁸O data in conjunction with chloride concentrations provide firm evidence for impact of dissolution of marine-origin evaporite deposits, during past geologic periods, on groundwater salinity in the northern region. Moreover, the relation between ¹⁴C activities and Cl^? concentration confirms this hypothesis.     

Use of isotopic tracers to characterize the interaction of water components and nitrate contamination in the arid Rasafeh area (Syria)

Chemical and isotopic data in atmospheric precipitation, surface water, and groundwater in arid Rasafeh area, northeast Syria, are used to clarify the status of groundwater quality, the interaction of water components, groundwater dating, and vulnerability to anthropogenic contamination. Interpretation of chemical data with thermodynamic calculation reveals that the dissolution of evaporate mineral is the main factor of high salinity. The δ¹⁸O and δ²H relationships indicate that the groundwater is fed by mixing water from Euphrates River and precipitation and the isotope balance equation were used to estimate the contribution of the Euphrates River to the aquifers recharge. High tritium content, together with high ¹⁴C activity in the majority of groundwater samples, indicate shorter residence times and consequently potentially greater recharge. The presence of high nitrate concentration associated with high tritium concentration in both shallow and deep aquifer units indicates the presence of high permeability, so that groundwater is highly susceptible to anthropogenic contamination. Nitrate seems to derive exclusively from the application of N fertilizers. The high nitrate values are characteristic of the areas with intensive agricultural activity, indicating the importance of irrigated return flow on the groundwater.     

Geochemistry of groundwater in the alluvial plain of Tucumán province, Argentina

The Salí River hydrogeological basin is one of the most productive artesian basins in Argentina. It is located in the southeastern part of the province of Tucumán, northwestern Argentina, 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. Three hydrochemical zones are defined in the study area and the processes that control the chemical composition of the water are manifestly different in each zone. The dissolution of halite, sodium sulphate, and gypsum explains part of the contained Na⁺, K⁺, Cl^–, SO₄ ^2–, and Ca²⁺, but other processes, such as cation exchange, calcite precipitation, weathering of aluminosilicates, and gas exchange with the atmosphere, also contribute to the water composition. The assessment of contamination indicators, such as pH, dissolved organic matter, dissolved oxygen, phosphate, and nitrate, indicates that the groundwater is suitable for human consumption. However, biological contamination has been detected in samples from some wells, especially those near the Salí River. Electronic Publication     

Groundwater flow and radioactivity in Namaqualand, South Africa

The Namaqualand area is located in the Northern Cape Province of South Africa which is characterised by arid climate where groundwater is the only source of water supply for local communities. Extensive groundwater sampling was carried out in the area and the physico-chemical parameters, inorganic constituents, stable isotopes and trace metals were measured. The hydrochemistry of the area indicates dissimilar groundwater composition due to complex geochemical processes where groundwater flow takes place from catchment F30A to the catchment D82B, and the chemistry is controlled primarily by Redox reaction, dissolution and mixing processes. The Br^?/Cl^? ratio revealed that the salinity in the area is derived from seawater mixing, halite dissolution and atmospheric deposition/sea aerosol spray. Under excessive evaporative condition due to climatic aridity, groundwater salinity shows increasing trend. Isotope results show the presence of shallow-weathered zone and deep-fracture controlled circulating groundwater in the crystalline basement aquifer of the area. In comparison to the South African water quality standard, the results obtained for gross alpha activity which could be derived from uranium isotopes show that 41 % of the reported data in the area fall above the drinking water limit.