松辽盆地油田地下水化学场的垂直分带性与平面分区性

松辽盆地地下水动力场的形成与演化控制了地下水化学场的形成与分布,地下水化学分布特征又反映地下水动力场的演化结果。在地下水化学场的形成过程中,影响沉积盆地地下水化学性质的因素较多,这些因素对地下水化学性质的影响作用在垂向上具有阶段性,在平面上具有选择性。前者导致地下水化学性质的垂直分带性,从浅到深可以划分出:1)大气水下渗淡化带,2)近地表蒸发浓缩带,3)泥岩压实排水淡化带(C₁)—压滤浓缩带(C₂),4)粘土矿物脱水淡化带和5)渗滤浓缩带等5种水化学剖面单元类型。后者决定了地下水化学场的平面分区性:1)盆地边缘为大气水下渗淡化区,2)盆地中央为泥岩压实排水淡化区,3)越流区为过渡区,4)越流-蒸发区为浓缩区。在泥岩压实排水形成的离心流方向上,矿化度、Na⁺浓度、Cl^-浓度和盐化系数升高,(CO₃^2-+HCO₃^-、SO₄^2-浓度、钠氯系数(γNa⁺/γCl^-)和脱硫系数(SO₄^2-/SO₄^2-+Cl^-)降低。在大气水下渗向心流方向上,矿化度、离子浓度和钠氯系数、脱硫系数和盐化系数一致升高。     

Geochemistry of groundwater in parts of Guntur district, Andhra Pradesh, India

Hydrogeochemical investigations, which are significant for the assessment of water quality, have been carried out to study the sources of dissolved ions in groundwaters of some rural areas of Guntur district, Andhra Pradesh, India. Groundwaters in the area are mostly brackish. High contents of SiO₂, and Na⁺ and Cl^- ions in groundwater, in comparison with those of seawater, suggests a meteoric origin of groundwater. The high concentration of SiO₂ and various geochemical signatures reflect the weathering of minerals. However, the Na⁺+K⁺ vs Cl^- ratio suggests weathering, has occurred only to some extent. The chemistry of groundwater favours the formation of clay minerals (montmorillonite, illite and chlorite), because of evapotranspiration. The positive saturation index of CaCO₃ and the high signatures of Ma²⁺:Ca²⁺ and Na⁺:Ca²⁺ reveals the occurrence of evaporation. The evaporation enhances the concentration of ions (which occurred originally in the water) in the soils during summer. The very high % MathType!MTEF!2!1!+- % feaaeaart1ev0aaatCvAUfKttLearuavTnhis1MBaeXatLxBI9gBae % bbnrfifHhDYfgasaacH8srps0lbbf9q8WrFfeuY-Hhbbf9v8qqaqFr % 0xc9pk0xbba9q8WqFfea0-yr0RYxir-Jbba9q8aq0-yq-He9q8qqQ8 % frFve9Fve9Ff0dmeaabaqaciGacaGaaeqabaqabeaadaaakeaacqqG % tbWucqqGpbWtdaqhaaWcbaGaeeinaqdabaGaeeOmaiJaeeyla0caaa % aa!2EC5! SO₄^{2 -} {\rm SO}_{\rm 4}^{{\rm 2 - }} and Cl^- contents in some groundwaters and the occurrence of kankar (CaCO₃) in the area suggest a long history of evaporation. Greater ionic concentration in the groundwaters of post-monsoon compared with pre-monsoon indicates the increasing addition of leachates into the groundwater from the soils in the monsoon and anthropogenic activities, which leads to a deteriorating quality of groundwater. According to the Gibbs' diagrams, rock weathering, to some extent, and evaporation are the dominant phenomena responsible for the higher ionic concentrations found in groundwater. Measures that benefit sustainable management of groundwater quality are suggested in this study.     

Water quality assessment and the investigation of the relationship between the River Delice and the aquifer systems in the vicinity of Yerköy (Yozgat,Turkey)

The aim of this study was to investigate the pollution parameters relating to surface and groundwaters and to establish an interaction between these for the area near Yerköy. Three characteristic facies were determined based on the results of hydrochemical analyses: (1) Na⁺-Cl^- facies were greater the deeper the aquifer, (2) Na⁺-SO₄^2- facies were the greater portion of the shallow alluvium aquifer, and (3) Na⁺-HCO₃^- (SO₄^2-) facies represented the western portion of the shallow alluvium aquifer. Based on field and laboratory observations it was found that the water of the River Delice is suitable for irrigation and domestic use whereas the water from the shallow aquifer is extremely saline and considered to have been polluted by local lithological units. Active groundwater circulation and dilution between the alluvium aquifer and the River Delice was observed. Because of the short residence time of the groundwater in this area, the hydrogeochemical concentration and the salinity were found to be low. The other portions of the alluvium aquifer bear higher concentrations of soluble ions.     

Hydrochemical and isotopic characteristics of groundwater in the Souss Upstream Basin, southwestern Morocco

Heterogeneous shallow Plio-Quaternary formations of the Souss Plain represent the most important aquifer in southern High Atlas Mountains in Morocco. The present work was conducted in the Souss Upstream Basin to identify the chemical characteristics and the origin of groundwater in an aquifer under semi-arid climate. Isotopic and hydrochemical compositions combined with geological and hydrogeological data were used for this purpose. The total dissolved solids vary from 239 to 997 mg l⁻¹, and the following groundwater types are recognized: Ca²⁺–Mg²⁺–HCO₃⁻, Ca²⁺–Mg²⁺–SO₄²⁻ and Ca²⁺–Mg²⁺–Cl⁻. The groundwater is saturated and slightly supersaturated with respect to carbonate minerals and undersaturated with respect to evaporite minerals, which means that the groundwater composition is largely controlled by the dissolution of carbonate rocks known in the basin. The isotopic contents of groundwaters ranged from −8‰ to −5.2‰ for δ¹⁸O, from −52‰ to −34‰ for δD, and from 0 to 5.5 TU for tritium. The hydrogen (δD) and oxygen (δ¹⁸O) isotope signatures reveal a significant infiltration before evaporation takes place, indicating a major recharge directly from fractures in the crystalline and limestone formations of Atlas Mountains (above 800 m a.s.l.) and infiltration of surface water in the alluvial cones at the border of the Atlas basins. The very low tritium values suggest that the groundwater recharge follows a long flow path and a mixing between old and modern water is shown. However, a slight evaporation effect is noted in the southern part of the basin close to the Anti-Atlas Mountains.     

Groundwater chemical and fecal contamination assessment of the Jerba unconfined aquifer,southeast of Tunisia

Located in the southeast of Tunisia, on the Mediterranean Sea, Jerba Island has a semiarid climate condition. The surface water scarcity has made groundwater the main source to supply the domestic, touristic, and agricultural water demand. Unconfined aquifer is a vulnerable costal aquifer system that undergoes several phenomena. This work aims at assessing the geochemical and bacteriological groundwater quality, defining groundwater pollution sources and promoting sustainable development and effective management of groundwater resources in Jerba Island. Data were collected after the wet season in 2014 from 79 wells. Electric conductivity, pH, TDS, and major and fecal tracers (total coliforms, thermotolerant coliforms, Escherichia coli, and Salmonella) were analyzed. Geochemical modeling including the relationships between geochemical tracers Na⁺ vs. Cl^?, Ca²⁺ vs. Cl^?, K⁺ vs. Cl^?, representative ionic ratios (Br^?/Cl^?, Na⁺/Cl^?, Mg²⁺/Ca²⁺), and statistical analysis were used to specify major process contributing to groundwater pollution and main factors controlling groundwater mineralization in the island. Groundwater varieties were hydrochemically classified into three types in terms of salinity values: group 1 (8.86%) to fresh water, group 2 (27.84%) to brackish water, and group 3 (63.29%) belongs to saline water. In addition, groundwater quality revealed high concentrations in chemical pollution tracers (Na⁺, Cl^?, SO₄ ^2?, and NO₃ ^?) and fecal tracers. Besides, most of the sampled wells were contaminated with nitrate (50.63%). Also, thermotolerant coliforms and E. coli were detected in all groundwater samples (96.2% of wells). Results indicated that the Jerba shallow aquifer was under serious threat from both natural and anthropogenic contamination. However, the wild discharge of domestic effluents, septic tanks, and sewage were the main origins of underground water contamination in Jerba Island. The reduction of fecal sources, through constructing normalized latrines is thus recommended.     

A regional study of saltwater intrusion in southeastern Nigeria based on the analysis of geoelectrical and hydrochemical data.

Vertical electrical sounding (VES) and hydrochemical data have been used to examine the extent of saltwater intrusion into shallow aquifers (depth<300 m) beneath the coastal plains of southeastern Nigeria underlain by siliciclastic sedimentary rocks of the Cenozoic Niger Delta. The VES data indicate that the coastal regions not affected by saltwater are characterised by K-and H-type geoelectrical curves and models in which high-layer resistivities (in excess of about 100 ohm-m) reflect the presence of freshwater aquifers at depths greater than 5 m below the surface. By contrast, Q-type curves and models denote saltwater-infiltrated islands with the upper boundary of the saline zone at depths of about 25 to 30 m. Chemical analysis results of precipitation and ground water show that, compared to coastal and continental sites, island localities have higher concentrations of major ions (Na⁺, K⁺, Ca²⁺, Mg²⁺, Cl^-, HCO₃^-, SO₄^2-, NO₃) due to saltwater intrusion. In addition, these ions, which also characterise seawater, show very good correlations (>0.70). Furthermore, the coastal sites are marked by Ca-Cl and Ca-HCO₃ water types whereas Na-Cl dominated both the islands ( at depths greater than 20 m) and the seawater. This gives an indication of seawater contamination. Seawater contamination is also indicated by the results of five assessment parameters as follows: high chloride concentration (>500 mg/l), high saturation index (halite>10^-6), high ionic strength (>0.05), low formation resistivity (<25 ohm-m), and low formation factor (<0.05). Two of these parameters (chloride concentration, ionic strength) have been used to compose an assessment scheme with five major classes (AA, BB, CC, DD, EE) corresponding to various degrees of salinity. Generally in the study area, saltwater contamination is a feature of island locations at depths greater than about 20 m. Water within the inland coastal regions is fresh.     

Deciphering the interaction between quaternary and continental Sabkhas aquifers in Central Tunisia using hydrochemical and isotopic tools

Climate aridity and intensive exploitation due to uncontrolled pumping for irrigation have caused a drastic decrease in the piezometric level of the shallow aquifer of Chougafiya plain, central Tunisia, and have seriously degraded groundwater quality. According to the hydrochemical data (Cl^?, SO₄ ^2?, NO₃ ^?, HCO₃ ^?, Br^?, Na⁺, Mg²⁺, K⁺, Ca²⁺, Sr²⁺) and the stable isotopes (¹⁸O and ²H content), groundwater salinization in the investigated aquifer is caused by four main processes: (1) evaporite dissolution (2) cation exchange reactions (3) evaporation processes and (4) mixing with Sabkhas salt water causing salinity to increase in the central and southern parts of the basin. The radiogenic (³H) isotope data provided insight into the presence of significant contemporaneous recharge waters in the western part of the shallow aquifer. The movement of the tritiated water may have occurred according to the general flow path (NW–SE). When tritium was used in conjunction with the stable isotopes and chloride, the mixing process could be clearly identified, especially in the central part of the study area.     

Surface-water quality for the Salí River watershed in NW Argentina

Spatial and temporal variations of Na, Mg, Si, K, Ca, SO₄^2-, Cl^-, HCO₃^-, Ag, Al, As, Au, B, Ba, Be, Bi, Br, Ce, Cd, Co, Cr, Cs, Cu, Dy, Er, Eu, F, Fe, Ga, Ge, Gd, Hf, Hg, Ho, I, La, Li, Mn, Mo, Nb, Nd, Ni, P, Pb, Pr, Rb, Sb, Sm, Sn, Sr, Ta, Tb, Te, Th, Ti, Tl, U, V, W, Y, Yb, Zn, and Zr were monitored through 37 sampling stations to determine the main aspects influencing the surface-water quality in the Salí River watershed (Tucumán Province, NW Argentina). The influence of the regional geological setting on water chemistry allows to distinguish three sub-basins. The interaction with sedimentary rocks was found to be dominant in the northern and central-eastern sub-basin as well as in the southern sub-basin, whereas the metamorphic-granitic basement of the Pampean Ranges was noted in the central sub-basin. In addition, anthropogenic activities affect the spatial variation of K, P, Mn, Rb, and Pb as well as dissolved oxygen concentrations and Eh. Temporal water-quality variation is related to the spatial distribution of precipitation and to the seasonal character of the main local industries (sugar cane, alcohol, citrus), increasing P and K concentrations and decreasing dissolved oxygen concentration and Eh in winter. Cl^-, Na, SO₄^2-, Al, As, B, Fe, Mn, Se and U concentrations exceed the regulated drinking-water thresholds at several sampling stations.     

Microchemical and Sr Isotopic Investigation of Zoned K-feldspar Megacrysts: Insights into the Petrogenesis of a Granitic System and Disequilibrium Crystal Growth

K-feldspar megacrysts (Kfm) are used to investigate the magmaticevolution of the 7 Ma Monte Capanne (MC) monzogranite (Elba,Italy). Dissolution and regrowth of Kfm during magma mixingor mingling events produce indented resorption surfaces associatedwith high Ba contents. Diffusion calculations demonstrate thatKfm chemical zoning is primary. Core-to-rim variations in Ba,Rb, Sr, Li and P support magma mixing (i.e. high Ba and P andlow Rb/Sr at rims), but more complex variations require othermechanisms. In particular, we show that disequilibrium growth(related to variations in diffusion rates in the melt) may haveoccurred as a result of thermal disturbance following influxof mafic magma in the magma chamber. Initial ⁸⁷Sr/⁸⁶Sr ratios(I_Sr) (obtained by microdrilling) decrease from core to rim.Inner core analyses define a mixing trend extending towardsa high I_Sr–Rb/Sr melt component, whereas the outer coresand rims display a more restricted range of I_Sr, but a largerrange of Rb/Sr. Lower I_Sr at the rim of one megacryst suggestsmixing with high-K calc-alkaline mantle-derived volcanics ofsimilar age on Capraia. Trace element and isotopic profilessuggest (1) early megacryst growth in magmas contaminated bycrust and refreshed by high I_Sr silicic melts (as seen in theinner cores) and (2) later recharge with mafic magmas (as seenin the outer cores) followed by (3) crystal fractionation, withpossible interaction with hydrothermal fluids (as seen in therim). The model is compatible with the field occurrence of maficenclaves and xenoliths. KEY WORDS: Elba; monzogranite; K-feldspar megacrysts; zoning; magma mixing; trace element; Sr isotopes; petrogenesis     

The chemistry of groundwater: A geoindicator of environmental change across the Polish-Lithuanian border

Groundwater monitoring in the Polish-Lithuanian cross-border area was launched in 1994, utilizing 24 monitoring stations. Of these, 20 are installed in aquifers in Quaternary tills, which are the main source of fresh water for centralized use and single households. Hydro-chemical sampling has been performed twice a year (spring and autumn) over a seven-year period, with determination of main chemical compounds. Hydrochemical differences on both sides of the border appear to be related to the type of land use. The groundwater quality on the Lithuanian side may have been influenced by anthropogenic factors operating prior to 1991 in the Soviet-type collective farms. The main trends over the monitoring period involve increase in SO₄²⁺and Cl^- ions on both sides of the border. The data demonstrate the importance of cross-border monitoring and exemplify groundwater chemistry as a direct geoindicator of the state of the environment.     

Estimating groundwater recharge beneath irrigated farmland using environmental tracers fluoride, chloride and sulfate

Accurate recharge estimation is essential for effective groundwater management, especially in the North China Plain, where irrigation return flow is significant to vertical recharge but brings difficulty for recharge estimation. Three environmental tracers (F^?, Cl^? and SO₄ ^2?) were used to estimate vertical recharge based on the mass balance and cumulative methods. Four boreholes were dry-drilled to 5–25 m depth beneath irrigated farmland and one was drilled to 5 m beneath non-irrigated woodland; soil samples were collected in all boreholes at set depths. The results indicated that F^?, Cl^? and SO₄ ^2?were suitable tracers beneath the non-irrigated woodland, yielding recharge rates of 16.9, 18.8 and 19.4 mm/year, respectively. Recharge estimation was not straightforward when taking account of crop type, irrigation and/or fertilizer use. After comparing with previous research, conclusions were drawn: Cl^? was an appropriate tracer for irrigated farmland when taking account of Cl^? input from irrigation and absorption by crops; recharge rates were 65.9–126.8 mm/year. However, F^? was a more suitable tracer for irrigated regions where account is made of the proportion of precipitation to irrigation return flow, provided low F^? concentrations can be measured reliably.     

Delineation of groundwater salinization in a coastal aquifer, Bousheher, South of Iran

The geochemical processes controlling chemical composition of groundwater are studied using hydrochemical and isotopic data in Abdan-Dayer coastal plain, south of Iran. The salinity of groundwater in the coastal plain ranges from 1,000, a fresh end-member, to more than 50,000 μS cm^?1, a saline end-member. Groundwater salinity increases from the recharge area toward areas with a shallow water table close to the Persian Gulf coast due to direct evaporation and sea water intrusion as confirmed by mixing binary diagrams, stable isotope content, and Br^?/Cl^? ratio. Groundwater flow pattern in the study area has been modified due to over-pumping of groundwater in recent years which resulted in further saline water migration toward fresh water and their mixing. The maximum mixing ratio is estimated about 15% in different parts of the study area according to chloride concentration.     

Present recharge of an aquifer in a semi-arid region: an example from the Turonian limestones of the Errachidia basin, Morocco

 The Errachidia basin is composed of three superposed aquifers (Senonian, Turonian limestones and Infracenomanian). The Liassic limestone of the upper Atlas borders the northern part of the basin. The piezometric map of the Turonian aquifer displays a north-south flow, with an inflow area from the Atlas. This recharge hypothesis is demontrated by a discriminant analysis performed on chemical data: the majority of the spots are of sodium choride and hydrogenocarbonate types, while several boreholes are assigned to a calcium hydrogenocarbonate type Jurassic component. ¹⁸O measurements, using the Atlasic gradient δ¹⁸O=–4.18–0.0027 x elevation to estimate the recharge areas, confirm that the recharge area is the basin itself (<1100 m) on the Turonian outcrops, while in the confined part, the Turonian is recharged higher than 1400 m (corresponding to the Atlas). This contribution ranges from 56 to 85%, according to the situation versus the piezometric inflow area. The remainder represents infiltration and vertical leakage from the Senonian layers.     

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.     

Statistical and hydrochemical methods to compare basalt- and basement rock-hosted groundwaters: Atherton Tablelands,north-eastern Australia

Multivariate analysis of physico-chemical and chemical data has enabled differentiation among groundwaters sourced from different lithological formations in the Atherton Tablelands region of north-eastern Australia. The main water resource is stored in basalt, although basement rocks such as granite and metamorphics also contain variable amounts of water. Groundwater in the basalt is mostly Mg-Ca-Na, HCO₃ type, with electrical conductivities less than 300 µS/cm and pH values from 6.5 to 8.5. Some of the other groundwater is quite similar, making the identification of hydrochemical facies difficult. Groundwater samples were grouped based on the results of a principal component factor analysis of the major dissolved constituents H₄SiO₄, Na⁺, Ca²⁺, Mg²⁺ and HCO₃^-, as well as pH and electrical conductivity. Based on this differentiation it was possible to identify the likely host rocks of groundwaters from unidentified lithological units, define the basalt thickness and provide a better understanding of the groundwater resource. Principal component factor analysis has also been useful in identifying the likely hydrochemical processes controlling the composition of these groundwaters, including the production of weak acids in the soil layers, silicate mineral weathering, ion-exchange reactions, evapotranspiration and the leaching of ions from organic matter. Supplementary material to this paper can be obtained by using the Springer LINK server located at http://dx.doi.org/10.1007/s00254-002-0667-z.     

Desalination of a sedimentary rock aquifer system invaded by Pleistocene Champlain Sea water and processes controlling groundwater geochemistry

The objective of this study was to identify geochemical processes and Quaternary geological events responsible for the variations in groundwater geochemistry observed in a sedimentary rock aquifer system, including brackish to saline groundwater. Inorganic constituents and environmental isotopes were analyzed for 146 groundwater samples. Dissolution of carbonates dominates in recharge areas, resulting in Ca-, Mg-HCO₃ groundwater. Further along flow paths, under confined conditions, Ca²⁺–Na⁺ ion exchange causes groundwater evolution to Na-HCO₃ type. Na-Cl groundwater is also found and it falls on a seawater mixing line. Using conservative tracers, Cl⁻ and Br⁻, the original Champlain Sea water is shown to have been, in the region, a mixture of about 34% seawater and 66% freshwater, a composition still retained by some groundwater. Na-Cl groundwater thus results from mixing with former Champlain Sea water and also from solute diffusion from overlying marine clay. The system is thus found to be at different stages of desalinization, from the original Champlain Sea water still present in hydraulically stagnant areas of the aquifer to fully flushed conditions in parts, where more flow occurs, especially in recharge zones. The geochemical processes are integrated within the hydrogeological context to produce a conceptual geochemical evolution model for groundwater of the aquifer system.     

Characterization of surface water and groundwater in the Damascus Ghotta basin: hydrochemical and environmental isotopes approaches

The hydrochemistry of major ions and environmental isotope compositions (¹⁸O, ²H and tritium) of water samples have been used to investigate the characteristics of rainfalls, surface water and groundwater in the Damascus Ghotta basin. The groundwater salinity in the Damascus Ghotta basin gradually increases, as the groundwater moves from western to south-eastern and north-eastern parts of the basin. A strong relationship exists between the Barada river and the surrounded groundwaters, mainly in terms of recharge by infiltration of surface waters. The groundwater quality in the Adra region has clearly become less saline as a result of establishment of the sewage-water-treatment station in this area since 1997. The uncommon depleted stable isotope concentrations in the vicinity of Al-Ateibeh Lake and Adra valley could be interpreted as a result of sub-flow recharge from the Cenomanian–Turonian aquifer, mostly prolonged along the Damascus Fault, which forms direct contact between this complex and the Quaternary alluvium aquifers. The extensive exploitation of water from the Cenomanian–Turonian aquifer for drinking water supply would shortly be reflected by a gradual decline of the groundwater table in the Damascus Ghotta basin. Amelioration of water quality in the Damascus basin still requires further management strategies and efforts to be taken within the forthcoming years.     

Hydrochemical and isotopic characterisation of the Bathonian and Bajocian coastal aquifer of the Caen area (northern France)

This paper describes the geochemical evolution of groundwater in the Bathonian and Bajocian aquifer along its flowpath. Since this aquifer represents one of the main sources of fresh water supply in the Caen area and has been subjected to a Holocene marine intrusion, its management requires a sound knowledge of (1) the primary conditions and (2) the potential influence of either natural or anthropogenic pressures. Groundwater vertical sampling validity is discussed with the contribution of high resolution temperature logging. The main processes of geochemical evolution along a groundwater flow line and the sea-water intrusion characteristics are discussed using ionic concentrations (Br⁻, F⁻ and major elements) and isotopes (water δ²H and δ¹⁸O, TDIC δ¹³C and A¹⁴C, sulphate δ¹⁸O and δ³⁴S). As the ¹³C content of TDIC is used as a tracer of water-rock interaction, it shows evidence of specific chemical and isotopic evolutions of groundwater within the aquifer, both related to water-rock interaction and mineral equilibria in groundwater. All the above-mentioned tracers evolve downflow: cation concentrations are modified by exchange with clay minerals allowing a high F⁻ concentration in groundwater, whereas Br⁻ and SO²⁻₄ concentrations appear to be redox condition dependant. Superimposed on these geochemical patterns, δ¹⁸O and δ²H compositions indicate that aquifer recharge has varied significantly through time. The chemical evolution of groundwater is locally affected by a salty water intrusion that is characterised by mixing between Flandrian fresh water and sea-water which has interacted with peat as evidenced by a high Br⁻/Cl⁻ ratio and SO²⁻₄ reduction.     

Effects of rainwater-harvesting-induced artificial recharge on the groundwater of wells in Rajasthan, India

In light of the increasing deterioration of groundwater supplies in Rajasthan, India, rainwater harvesting practices in southern Rajasthan were studied to determine the effects of artificially recharged groundwater on the supply and quality of local groundwater. A physical and geochemical investigation utilizing environmental tracers (δ¹⁸O and Cl^–), groundwater level and groundwater quality measurements, and geological surveys was conducted with two objectives: (1) to quantify the proportion of artificially recharged groundwater in wells located near rainwater harvesting structures and (2) to examine potential effects of artificial recharge on the quality of groundwater in these wells. A geochemical mixing model revealed that the proportion of artificial recharge in these wells ranged from 0 to 75%. Groundwater tracer, water table, and geological data provided evidence of complex groundwater flow and were used to explain the spatial distribution of artificial recharge. Furthermore, wells receiving artificial recharge had improved groundwater quality. Statistical analysis revealed a significant difference between the water quality in these wells and wells determined not to receive artificial recharge, for electrical conductivity and SO ₄ ^– . The findings from this study provide quantitative evidence that rainwater harvesting structures in southern Rajasthan influence the groundwater supply and quality of nearby wells by artificially recharging local groundwater.     

Hydrogeochemical and isotopic characterizations of an aquifer in the semi-arid region of the Mexican Highlands

This work addresses hydrogeochemical processes in shallow aquifers, represented by the Quaternary alluvial deposits, from a part of the semi-arid Mexican Highlands through the evaluations of physicochemical parameters as well as the δ¹⁸O and δ²H compositions of groundwater. Mifflin diagram separates the Na-bicarbonate, sulphate and mixed groundwater into one group showing interactions with volcanic lithology in the recharge zones and another group interacting with the evaporite rich sedimentary formation. In the Gibbs diagram, the samples with Cl^?/(Cl^? + HCO₃^?) < 0.4 showed higher influence of ion exchange and the samples with Cl^?/(Cl^? + HCO₃^?) > 0.4 showed higher effects of evaporation. All of them were oversaturated with carbonate minerals (i.e., calcite and dolomite) and unsaturated with evaporites (i.e., gypsum and halite). Evaporation (earlier stage) occurred before the water-rock interactions (later stage). Evolution occurs through three different routes such as up to 7.5‰ enrichment in δ¹⁸O caused by the infiltration with a certain delay and subsequently, the water-rock interaction became dominant. Ternary mixing models revealed dominant influence of local recharge (C₁) on the water system, contributing 70.4%. Water-rock interaction (C₃) with 18% and evaporation (C₂) with 11.6% had comparatively less influences. The presence of nitrate (2–60 mg/L) in the groundwater indicated variable degrees of anthropogenic pollution.