Groundwater chemistry of strike slip faulted aquifers: the case study of Wadi Zerka Ma’in aquifers, north east of the Dead Sea

Wadi Zerka Ma’in catchment area is located to the north east of the Dead Sea. It has two types of aquifers: (a) an upper unconfined aquifer and (b) a lower confined aquifer. The two aquifers are separated by a marl aquiclude. A major strike slip fault passes perpendicularly through the two aquifers and the aquiclude layer with embedded normal faults. The aim of the study was to specify the effect of the major strike slip fault on the groundwater chemistry. The spatial variability of the hydrochemical compositions and physiochemical parameters of the groundwater were investigated. It was found that the embedded normal faults, of the strike slip fault, form conduits that allow groundwater to flow from the lower aquifer to the upper aquifer, resulting in mixed groundwater. The ratio of mixing was estimated to be 94 % groundwater from the upper aquifer and 6 % from the lower aquifer. Since groundwater in the lower aquifer is around three times more saline than the upper aquifer, water mixing into the upper water aquifer generates a salinity hazard.     

Origin of groundwater salinity (current seawater vs. saline deep water) in a coastal karst aquifer based on Sr and Cl isotopes. Case study of the La Clape massif (southern France)

In this study a typical coastal karst aquifer, developed in lower Cretaceous limestones, on the western Mediterranean seashore (La Clape massif, southern France) was investigated. A combination of geochemical and isotopic approaches was used to investigate the origin of salinity in the aquifer. Water samples were collected between 2009 and 2011. Three groundwater groups (A, B and C) were identified based on the hydrogeological setting and on the Cl⁻ concentrations. Average and maximum Cl⁻ concentrations in the recharge waters were calculated (Cl_Ref. and Cl_Ref.Max) to be 0.51 and 2.85 mmol/L, respectively). Group A includes spring waters with Cl⁻ concentrations that are within the same order of magnitude as the Cl_Ref concentration. Group B includes groundwater with Cl⁻ concentrations that range between the Cl_Ref and Cl_Ref.Max concentrations. Group C includes brackish groundwater with Cl⁻ concentrations that are significantly greater than the Cl_Ref.Max concentration. Overall, the chemistry of the La Clape groundwater evolves from dominantly Ca–HCO₃ to NaCl type. On binary diagrams of the major ions vs. Cl, most of the La Clape waters plot along mixing lines. The mixing end-members include spring waters and a saline component (current seawater or fossil saline water). Based on the Br/Cl_molar ratio, the hypothesis of halite dissolution from Triassic evaporites is rejected to explain the origin of salinity in the brackish groundwater.Groundwaters display ⁸⁷Sr/⁸⁶Sr ratios intermediate between those of the limestone aquifer matrix and current Mediterranean seawater. On a Sr mixing diagram, most of the La Clape waters plot on a mixing line. The end-members include the La Clape spring waters and saline waters, which are similar to the deep geothermal waters that were identified at the nearby Balaruc site. The ³⁶Cl/Cl ratios of a few groundwater samples from group C are in agreement with the mixing hypothesis of local recharge water with deep saline water at secular equilibrium within a carbonate matrix. Finally, PHREEQC modelling was run based on calcite dissolution in an open system prior to mixing with the Balaruc type saline waters. Modelled data are consistent with the observed data that were obtained from the group C groundwater. Based on several tracers (i.e. concentrations and isotopic compositions of Cl and Sr), calculated ratios of deep saline water in the mixture are coherent and range from 3% to 16% and 0% to 3% for groundwater of groups C and B, respectively.With regard to the La Clape karst aquifer, the extension of a lithospheric fault in the study area may favour the rise of deep saline water. Such rises occur at the nearby geothermal Balaruc site along another lithospheric fault. At the regional scale, several coastal karst aquifers are located along the Gulf of Lion and occur in Mezosoic limestones of similar ages. The ⁸⁷Sr/⁸⁶Sr ratios of these aquifers tend toward values of 0.708557, which suggests a general mixing process of shallow karst waters with deep saline fossil waters. The occurrence of these fossil saline waters may be related to the introduction of seawater during and after the Flandrian transgression, when the highly karstified massifs invaded by seawater, formed islands and peninsulas along the Mediterranean coast.     

Groundwater resource sustainability in the Wadi Watir delta, Gulf of Aqaba, Sinai, Egypt

The Wadi Watir delta, in the arid Sinai Peninsula, Egypt, contains an alluvial aquifer underlain by impermeable Precambrian basement rock. The scarcity of rainfall during the last decade, combined with high pumping rates, resulted in degradation of water quality in the main supply wells along the mountain front, which has resulted in reduced groundwater pumping. Additionally, seawater intrusion along the coast has increased salinity in some wells. A three-dimensional (3D) groundwater flow model (MODFLOW) was calibrated using groundwater-level changes and pumping rates from 1982 to 2009; the groundwater recharge rate was estimated to be 1.58?×?10⁶ m³/year. A variable-density flow model (SEAWAT) was used to evaluate seawater intrusion for different pumping rates and well-field locations. Water chemistry and stable isotope data were used to calculate seawater mixing with groundwater along the coast. Geochemical modeling (NETPATH) determined the sources and mixing of different groundwaters from the mountainous recharge areas and within the delta aquifers; results showed that the groundwater salinity is controlled by dissolution of minerals and salts in the aquifers along flow paths and mixing of chemically different waters, including upwelling of saline groundwater and seawater intrusion. Future groundwater pumping must be closely monitored to limit these effects.     

Processes affecting groundwater chemistry in a zone of saline intrusion into an urban sandstone aquifer

Samples have been collected from inflows into railway tunnels in the Triassic sandstone aquifer beneath Liverpool and the Mersey Estuary, England, U.K. These provide a profile through a saline–freshwater mixing zone. Analyses were made of major anions and cations, δ³⁴S and δ¹⁸O in SO₄, δ¹³C in dissolved inorganic C and ⁸⁷Sr/⁸⁶Sr. The data demonstrate that the presence of a low permeability fault exerts a strong control on the local groundwater chemistry. On the estuary side of the fault, groundwater chemistry is dominated by mixing of intruding estuary water, which is modified by SO₄ reduction and calcite dissolution, with fresh groundwater. The environment of SO₄ reduction in the tidal estuary is one of repeated reduction and re-oxidation of S in an open system and has resulted in virtually no change in S isotopic composition, but an enrichment in residual SO₄ δ¹⁸O of 1.5‰. Groundwater chemistry on the landward side of the fault is primarily the result of recharge in an urban environment. There is also evidence that saline water has been present in this region of the aquifer in the past and that this has now been flushed by fresh groundwaters. This saline water was either transported along the landward side of the fault from nearer the estuary or more probably transmitted across the fault. Both mechanisms would have been driven by large landward head gradients caused by heavy industrial abstraction earlier this century. This has produced a zone of groundwaters depleted in Ca and radiogenic Sr and enriched in Na as a result of ion exchange between the fresh groundwaters and the aquifer previously occupied by more saline water. Sulphur isotopic composition, however, shows no variation since SO₄ does not undergo significant ion exchange. A tracer test from a borehole to the tunnels showed multiple breakthroughs to some locations indicating a number of different flow paths through the aquifer. The maximum flow velocity recorded in this test was 140 m/d suggesting flow along fractures.     

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).     

Genesis and distribution of mineral waters as a consequence of recent lithospheric dynamics: the Rhenish Massif,Central Europe

Three major, interdependent processes control the genesis and distribution of mineral and thermal waters in the Rhenish Massif, Central Europe: (a) Magmatic processes in the upper mantle provide most of the CO₂ to produce bicarbonate waters in shallow aquifers. (b) Extension of the brittle upper crust enables the ascent of sodium chloride waters. (c) Uplift and erosion shape the massif's relief, which determines the extent of flow systems and the distribution of thermal springs. The chemistry of mineral waters further depends on the aquifers' mineral composition. A comprehensive set of hydrological, chemical, tectonic and geophysical data on the Rhenish Massif has been compiled. It was used to classify the mineral waters and to map the spatial distribution of water properties. The composition of cuttings from several representative wells producing different water types shows that the hydrothermal alteration of the aquifer rocks consists mainly of kaolinization of chlorite and dissolution of feldspar. Numerical transport simulations favour two modes of groundwater flow: topography-driven flow and the pressure-driven ascent of basement brines along active faults. Thermal convection is less important.     

Modeling of limestone aquifer in the western part of the River Nile between Beni Suef and El Minia

A robust classification scheme for partitioning groundwater chemistry into homogeneous groups was an important tool for the characterization of Eocene limestone aquifer. The aquifer locally is composed of chalky limestone with thin clay intercalated (Samalut Fm.), the fissures, the joints, and the fractures are represented the conduits of the aquifer system. The flow patterns are conditioned by karstification processes which develop a conduit network and preserve low permeability microfractured blocks. The aquifer is mainly recharged by surrounding aquifers and agricultural wastewaters. The groundwater flows in the eastern part (due the Bahr Yossef and River Nile), which is a discharge area rather than a recharge. Twenty-eight groundwater samples was collected from the Eocene limestone aquifer and analyzed for isotopes, major, and trace elements. δD and δ¹⁸O concentrations ranged widely due to geology, infiltration of different surface waters, evaporation, and hydrogeology. The concentration of δD and δ¹⁸O isotopes is depleted in the northern zone of the northern part and western zone of the central and southern part of the study area. They are enriched due the eastern area of the central and southern part of the study area. δD vs. δ¹⁸O delineate the Pleistocene aquifer and has a strong influence than other waters on aquifer hydrogeochemistry. It is confirmed by the AquaChem outputs of the mixing proportions of different water types included in the aquifer system. Cl-δD and Cl-δ¹⁸O relationships indicate the role of evaporation especially due the eastern area of the central and southern part of the study area. This research tests the performance of the many available graphical and statistical methodologies used to classify water samples. R-mode clustering, correlation analysis, and principal component analysis were investigated. All the methods were discussed and compared as to their ability to cluster, ease of use, and ease of interpretation. Nearly most low-salinity waters are in equilibrium to supersaturate with respect to both carbonate minerals, while it is shifted to undersaturate with salinity. The inverse modeling findings clarify that the calcite, gypsum, and anhydrite dissolution increased due the northeastern area, middle zone, and southern corner of the northern, central, and southern part of the study area, respectively. The latter areas also were characterized by the lowest precipitation of the dolomite. Such areas are distinguished by much more enhancement for aquifer permeability and therefore transmissivity. The latter areas can be use as injection zone by fresh water. It can be a triple function; firstly, it recharges the saline Eocene limestone aquifer through the enhancement hydraulic conductivity and dilutes it. Secondly, it enhances much more the aquifer permeability and therefore the transmissivity. The Eocene limestone aquifer can be improved in quality and quantity by using such a model and exploits it as an alternative water resource with Quaternary aquifer and Nile water. Thirdly, it irrigates more areas to increase the income/capita. The dedolomitization represents the main hydrogeochemical process in the aquifer system. The geomedia (limestone, clay, marl, shale, and sand deposits) are in contact with water, therefore, the rock/water interaction, mixing, and ion exchange were estimated by the geochemical evolution of the groundwater systems.     

Mixing of shallow and deep groundwater as indicated by the chemistry and age of karstic springs

Large karstic springs in east-central Florida, USA were studied using multi-tracer and geochemical modeling techniques to better understand groundwater flow paths and mixing of shallow and deep groundwater. Spring water types included Ca–HCO₃ (six), Na–Cl (four), and mixed (one). The evolution of water chemistry for Ca–HCO₃ spring waters was modeled by reactions of rainwater with soil organic matter, calcite, and dolomite under oxic conditions. The Na–Cl and mixed-type springs were modeled by reactions of either rainwater or Upper Floridan aquifer water with soil organic matter, calcite, and dolomite under oxic conditions and mixed with varying proportions of saline Lower Floridan aquifer water, which represented 4–53% of the total spring discharge. Multiple-tracer data—chlorofluorocarbon CFC-113, tritium (³H), helium-3 (³He_trit), sulfur hexafluoride (SF₆)—for four Ca–HCO₃ spring waters were consistent with binary mixing curves representing water recharged during 1980 or 1990 mixing with an older (recharged before 1940) tracer-free component. Young-water mixing fractions ranged from 0.3 to 0.7. Tracer concentration data for two Na–Cl spring waters appear to be consistent with binary mixtures of 1990 water with older water recharged in 1965 or 1975. Nitrate-N concentrations are inversely related to apparent ages of spring waters, which indicated that elevated nitrate-N concentrations were likely contributed from recent recharge.The online version of the original article can be found at     

川西南喜德热田地下水水文地球化学特征

地下热水的形成和化学组分特征常受断裂构造和热储地层岩性的影响。川西南喜德地热田内出露的冷泉水和地热水严格受断裂控制,前者为主断裂控制的浅循环型碎屑岩或岩溶裂隙孔隙水;后者则为次级断裂所控制的深循环型裂隙水,其热储层为碳酸盐岩。基于喜德热田形成的地质构造背景,通过开展热田内地热水和冷泉水水化学指标的测试和分析及水岩相互作用模拟,对该热田水文地球化学特征进行了研究。结果表明：喜德热田地热水和冷泉水水源均为大气降水,补给高程分别为2 874~3 092 m和2 584~2 818 m。受温度、含水层矿物类型、水岩相互作用的影响,地热水和冷泉水水化学类型和各组分差别较大,前者为HCO3·SO4-Ca·Mg型水,后者为HCO3-Ca·Mg型水。水岩相互作用模拟表明碳酸盐岩矿物、石膏矿物的溶解和沉淀及阳离子交换过程是导致地热水和冷泉水水化学组分差别较大的主要原因。此外,采用二氧化硅类温标计算喜德热田热储温度为56~90 ℃,循环深度为1 422~2 558 m。研究结果对阐明喜德热田的成因模式,地热水的进一步开发和热水资源的可持续利用具有重要意义。     

Mixing of shallow and deep groundwater as indicated by the chemistry and age of karstic springs

Large karstic springs in east-central Florida, USA were studied using multi-tracer and geochemical modeling techniques to better understand groundwater flow paths and mixing of shallow and deep groundwater. Spring water types included Ca–HCO₃ (six), Na–Cl (four), and mixed (one). The evolution of water chemistry for Ca–HCO₃ spring waters was modeled by reactions of rainwater with soil organic matter, calcite, and dolomite under oxic conditions. The Na–Cl and mixed-type springs were modeled by reactions of either rainwater or Upper Floridan aquifer water with soil organic matter, calcite, and dolomite under oxic conditions and mixed with varying proportions of saline Lower Floridan aquifer water, which represented 4–53% of the total spring discharge. Multiple-tracer data—chlorofluorocarbon CFC-113, tritium (³H), helium-3 (³He_trit), sulfur hexafluoride (SF₆)—for four Ca–HCO₃ spring waters were consistent with binary mixing curves representing water recharged during 1980 or 1990 mixing with an older (recharged before 1940) tracer-free component. Young-water mixing fractions ranged from 0.3 to 0.7. Tracer concentration data for two Na–Cl spring waters appear to be consistent with binary mixtures of 1990 water with older water recharged in 1965 or 1975. Nitrate-N concentrations are inversely related to apparent ages of spring waters, which indicated that elevated nitrate-N concentrations were likely contributed from recent recharge.An erratum to this article can be found at     

Groundwater components in the alluvial aquifer of the alpine Rhone River valley, Bois de Finges area, Wallis Canton, Switzerland

Source, type, and quantity of various components of groundwater, as well as their spatial and temporal variations were determined by different hydrochemical methods in the alluvial aquifer of the upper Rhone River valley, Bois de Finges, Wallis Canton, Switzerland. The methods used are hydrochemical modeling, stable-isotope analysis, and chemical analysis of surface water and groundwater. Sampling during high- and low-water periods determined the spatial distribution of the water chemistry, whereas monthly sampling over three years provided a basis for understanding seasonal variability. The physico-chemical parameters of the groundwater have spatial and seasonal variations. The groundwater chemical composition of the Rhone alluvial aquifer indicates a mixing of weakly mineralized Rhone River water and SO₄-rich water entering from the south side of the valley. Temporal changes in groundwater chemistry and in groundwater levels reflect the seasonal variations of the different contributors to groundwater recharge. The Rhone River recharges the alluvial aquifer only during the summer high-water period. Electronic Publication     

The Pliocene Yafo Formation in Israel: Hydrogeologically inert or active?

For several decades the “Saqiye beds” (later renamed Yafo Formation) underlying the Coastal Plain aquifer (Kurkar Group) aquifer of Israel, were regarded as an extremely thick, tectonically undisturbed, and absolutely impervious aquiclude. Following intensive groundwater exploitation from the overlying Kurkar Group aquifer, brackish and saline waters were locally encountered in the lower parts of this aquifer and always at the contact with the underlying Yafo Formation aquiclude. The present study revealed that this aquiclude is not a uniform and impervious rock unit, but rather an alternation of pervious and impervious strata within the Yafo Formation containing highly pressured fluids of different — mostly high — salinities. The permeable beds are at an angular unconformity and in direct contact with the overlying Kurkar Group aquifer. The Yafo Formation and the underlying and overlying rock units are dislocated by numerous fault systems, which facilitate accessibility of brines into the Kurkar Group aquifer. The mobilization of the saline fluids and their injection into the Kurkar Group aquifer could be due either to diffusion of saline fluids occurring in the permeable horizons of the Petah Tiqva Member through the clays of the Yafo Formation or to their upconing following intensive pumping in the Coastal Plain aquifer. It could have also been caused by up-dip movement of saline water as the result of overpressure generated by major accumulation of gas in the permeable horizons. Another possible mechanism could be hydraulic contact with pressurized brines up-flowing along fault zones from deep-seated Jurassic or Cretaceous reservoirs. The squeezing of saline interstitial water from the clays of the Yafo Formation into the overlying Kurkar Group aquifer, is of secondary importance for groundwater salinization (its input is comparable with salt input from rain).     

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.     

Deep groundwater in the crystalline basement of the Black Forest region

Two major types of groundwater can be readily distinguished in the Variscian crystalline basement of the Black Forest in S–W Germany. Saline thermal water utilized in spas has its origin in 3–4 km deep reservoirs and developed its composition by 3 component mixing of surface freshwater, saltwater (of ultimately marine origin) and a water–rock reaction component. In contrast to the thermal water, CO₂-rich mineral water, tapped and bottled from many wells in the Black Forest, has low salinities but a TDS distribution similar to that of thermal water. It developed its chemical composition entirely by reaction of CO₂-rich water with the gneissic or granitic aquifer rock matrix. Particularly important is the contribution of various plagioclase dissolution and weathering reactions that may, at some locations, involve precipitation and dissolution of secondary calcite. Sodium/Ca ratios of water and of rock forming plagioclase in the basement rocks suggests that plagioclase weathering is strongly incongruent. Calcium is released to the water, whereas Na remains fixed to the albite feldspar component.The major element composition of 192 water samples used in this study also indicates a clear vertical stratification of the type of water chemistry; Ca–HCO₃ near the surface, Na–Ca–HCO₃–SO₄ at intermediate depth and Na–Ca–Cl at great depth.The mean permeability of Black Forest granite is about K=10⁻⁶ m/s; it is significantly lower in gneisses (gneiss: mean K=5×10⁻⁸ m/s) leading to focused flow through granite. Highly permeable fracture and fault zones, particularly in granite, are utilized by high-TDS saline deep groundwater as ascent channels and flow paths. Although spatially closely associated, the topography driven upwelling system of saline deep water and the near-surface flow system of CO₂-rich mineral waters are hydraulically and chemically unconnected.     

Multivariate statistical analyses of the groundwater system in Darb El-Arbaein, Southwestern Desert, Egypt

In Darb El-Arbaein, the groundwater is the only water resource. The aquifer system starts from Paleozoic–Mesozoic to Upper Cretaceous sandstone rocks. They overlay the basement rocks and the aquifer is confined. In the present research, the performance of the statistical analyses to classify groundwater samples depending on their chemical characters has been tested. The hydrogeological and hydrogeochemical data of 92 groundwater samples were obtained from the General Authority for Rehabilitation Projects and Agricultural Development authority in northern, central, and southern Darb El-Arbaein. A robust classification scheme for partitioning groundwater chemistry into homogeneous groups was an important tool for the characterization of Nubian sandstone aquifer. We test the performance of the many available graphical and statistical methodologies used to classify water samples. R-mode, Q-mode, correlation analysis, and principal component analysis were investigated. All the methods were discussed and compared as to their ability to cluster, ease of use, and ease of interpretation. The correlation investigation clarifies the relationship among the lithologic, hydrogeologic, and anthropogenic factors. Factor investigation revealed three factors, namely, the evaporation process–agricultural impact–lithogenic dissolution, the hydrogeological characteristics of the aquifer system, and the surface meteoric water that recharge the aquifer system. Two main clusters that subdivided into four subclusters were identified in the groundwater system based on hydrogeological and hydrogeochemical data. They reflect the impact of geomedia, hydrogeology, geographic position, and agricultural wastewater. The groundwater is undersaturated with respect to most selected minerals. The groundwater was supersaturated with respect to iron minerals in northern and southern Darb El-Arbaein. The partial pressure of the groundwater versus saturation index of calcite shows the gradual change in PCO₂ from atmospheric to the present aquifer pressures.     

Hydrogeochemical evolution of the shallow and deep basaltic aquifers in Tamborine Mountain,Queensland (Australia)

Tamborine Mountain, Queensland (Australia), is a prime example of a basalt fractured-rock aquifer. Yet very little is known about the hydrochemistry of this groundwater system. Both analytical (major ions and stable isotopes) and multivariate (hierarchical cluster analysis, principal component analysis and factor analysis) analyses were used in this study to investigate the factors that interact within this aquifer system, in order to determine groundwater hydrogeochemistry. A new approach was applied to the data by classifying hydrographs by water type to clearly identify differing aquifer zones. Three distinct groundwater chemistry types were identified, and they were differentiated by variations in depth. Shallow bores were dominated by Na–Cl waters, deep bores were dominated by Na–HCO₃ and Ca–HCO₃ waters, and the two deepest bores were dominated by mixed water types. The evaluation of hydrogeochemical data has determined that both mineral weathering processes and groundwater/surface-water interaction had a strong influence on the hydrogeochemistry. Seasonal effects were minimal in the study area based on physicochemical parameters and ion chemistry. However, stable isotopic data show temporal trends. Increased rainfall events during the wet season produced a depletion in δ¹⁸O and increased d-excess values. The opposite is found during the dry season as a result of higher evaporation rates that are not hindered by intense rainfall events.

     

Hydrochemical and isotopic characterisation of groundwaters to define aquifer type and connectivity in a subtropical coastal setting,Fraser Coast,Queensland

Physico-chemical parameters, major ion chemistry and isotope composition of surface and groundwaters were determined in forested coastal catchments and adjacent coastal plains. Results showed obvious characterisation related to physical and hydrological setting, and highly variable spatial differences reflecting the complexities of these areas. All these coastal waters are dominated by Na–Cl and fall on a common dilution line; hydrochemical grouping is largely due to anionic differences (Cl, SO₄ and HCO₃), although Na and Mg ratios also vary. Six major hydrochemical facies were determined. For groundwaters, compositional differences are largely related to aquifer material and level of confinement; for coastal groundwaters important are tidal effects and proximity to the shoreline. Differentiation for surface waters is mainly by drainage morphology, flow regime plus proximity to the coast. Connectivity between water bodies is reflected by minor base flow to catchment streams, including with flood plain wetlands, but mostly occurs in low-lying zones where there is mixing of fresh and saline water within surface water and subterranean estuaries, or by seawater intrusion enhanced by overuse. Oxygen and hydrogen isotopic data for confined and semi-confined groundwaters along the coast indicates local recharge; fresh surface waters in the elevated catchments are shown to be sourced further inland plus have experienced evaporation.     

The changes of groundwater chemistry of semi-confined buried valley aquifer during one decade of water exploitation

This article presents the analysis of the temporal changes in water chemistry in a semi-confined aquifer (Wielkopolska Buried Valley aquifer, Poland) during one decade of water exploitation. It is shown that the groundwater contamination, as documented in a previous work, still persists and has lead to steady groundwater quality deterioration. The most intensive changes in water chemistry due to contamination are observed in the regions recognized earlier as the most vulnerable parts of the aquifer. The influence of contamination is effective despite implementation of groundwater protection activities. The travails of groundwater quality protection of the confined or semi-confined aquifers were accented.     

Contributions of boron isotopes to understanding the hydrogeochemistry of the coastal detritic aquifer of Castellón Plain,Spain

The Castellón Plain alluvial aquifer, Spain, is intensively exploited to meet the demand for agricultural irrigation and industrial water supply. The geochemistry of its groundwater shows complex salinization in the northern and southern parts of the aquifer, with significant pollution from human origin in the central portion. Boron content and B isotope geochemistry are useful for distinguishing between various sources of pollution and their relative importance in different parts of this aquifer. Boron concentrations in the groundwater vary between 0.01 and 0.85 mg/L. In the more saline groundwaters, found at the northern and southern ends of the study area, the presence of B is linked to inputs from seawater and water with a calcium-magnesium sulphate facies, which feed the aquifer and clearly influence the chemistry of its waters. Evidence of B adsorption processes in some samples is shown by the low B/Cl ratios and the high values of δ¹¹B. In the central portion of the aquifer, the high B/Cl ratios and the strongly negative δ¹¹B are related to pollution of human origin.     

Geochemistry of regional aquifer systems hosted by carbonate-evaporite formations in Umbria and southern Tuscany (central Italy)

In central Italy Mesozoic carbonates represent the principal reservoir of freshwater of the region. The hydrogeological setting is linked to the geological evolution of the Apennine chain and is generally characterised by a lower aquifer and one or more shallower aquifers separated by thin aquicludes. In these systems, groundwater composition is the result of a complex array of regional and local geochemical processes. The main geochemical processes are the dissolution of calcite, the influx of deeply derived CO₂ related to a regional process of mantle degassing, dedolomitization and mixing with deep saline fluids. The occurrence of saline fluids, characterised by a Na–Cl(HCO₃) composition, is related to the presence of a deep regional aquifer at the base of Mesozoic carbonates. The extremely high pCO₂ values computed for the saline waters suggest that the deep aquifer is also a structural trap for the mantle derived CO₂ during its ascent towards the surface. In central Italy, geological and geophysical data highlight the presence of two different crustal sectors: the eastern sector, where the geometry of the Apennine thrust belt is still preserved, and the western sector, where the compressive structures are dislocated by important extensional deformations. In the western sector, the normal faults disrupting the compressive structures allow the mixing of the deep Na–Cl(HCO₃) fluids with the shallow groundwater causing a salinity increase and the natural deterioration of groundwater quality.