Groundwater recharge and evolution of water quality in China’s Jilantai Basin based on hydrogeochemical and isotopic evidence

We investigated major ions, stable isotopes, and radiocarbon dates in a Quaternary aquifer in semi-arid northwestern China to gain insights into groundwater recharge and evolution. Most deep and shallow groundwater in the Helan Mountains was fresh, with total dissolved solids <1,000 mg L^?1 and Cl^? <250 mg L^?1. The relationships of major ions with Cl^? suggest strong dissolution of evaporites. However, dissolution of carbonates, albite weathering, and ion exchange are also the major groundwater process in Jilantai basin. The shallow desert groundwater is enriched in δ¹⁸O and intercepts the local meteoric water line at δ¹⁸O = ?13.4 ‰, indicating that direct infiltration is a minor recharge source. The isotope compositions in intermediate confined aquifers resemble those of shallow unconfined groundwater, revealing that upward recharge from intermediate formations is a major source of shallow groundwater in the plains and desert. The estimated residence time of 10.0 kyr at one desert site, indicating that some replenishment of desert aquifers occurred in the late Pleistocene and early Holocene with a wetter and colder climate than at present.     

Characterisation of groundwater recharge conditions and flow mechanisms in bedrock aquifers of the Johannesburg area,South Africa

Groundwater is the major source of water and a critical resource for socioeconomic development in semi-arid environments like the Johannesburg area. Environmental isotopes are employed in this study to characterise groundwater recharge and flow mechanisms in the bedrock aquifers of Johannesburg, which is known for polluted surface water. With the exception of boreholes near the Hartbeespoort Dam, groundwater in the study area was derived from meteoric water that has undergone some degree of evaporation before recharge, possibly via diffuse mechanisms. Boreholes that tap groundwater from the Transvaal Supergroup Formation show depletion in δ¹⁸O and δ²H values. This is attributed to diffuse recharge through weathering fractures at high elevation that are undergoing deep circulation or recharge from depleted rainfall from the high-latitude moisture sources. The influence of focused recharge from the Hartbeespoort Dam was observed in the boreholes north of the dam, possibly as a result of the north–south trending fault lines and the north-dipping fractures in the bedding planes of quartzites. This is also supported by a reservoir water budget method which indicated a mean annual net flux of 2,084,131 m³ from Hartbeespoort Dam recharging groundwater per annum. Using tritium in the dam and boreholes located at 750 m and 5400 m downstream, average groundwater flow velocity was estimated as 202 m/year. An open system was observed in shale, andesite and granitic-gneiss aquifers indicating soil CO₂ as a dominant source of carbon (δ¹³C) in groundwater. A closed system was also observed in dolomitic aquifers indicating carbonate dissolution as the predominant source of carbon.     

Mechanism of fluoride enrichment in groundwater of hard rock aquifers in Medak,Telangana State,South India

A total of 194 groundwater samples were collected from wells in hard rock aquifers of the Medak district, South India, to assess the distribution of fluoride in groundwater and to determine whether this chemical constituent was likely to be causing adverse health effects on groundwater user in the region. The study revealed that the fluoride concentration in groundwater ranged between 0.2 and 7.4 mg/L with an average concentration of 2.7 mg/L. About 57% of groundwater tested has fluoride concentrations more than the maximum permissible limit of 1.5 mg/L. The highest concentrations of fluoride were measured in groundwater in the north-eastern part of the Medak region especially in the Siddipeta, Chinnakodur, Nanganoor and Dubhaka regions. The areas are underlain by granites which contain fluoride-bearing minerals like apatite and biotite. Due to water–rock interactions, the fluoride has become enriched in groundwater due to the weathering and leaching of fluoride-bearing minerals. The pH and bicarbonate concentrations of the groundwater are varied from 6.6 to 8.8 and 18 to 527 mg/L, respectively. High fluoride concentration in the groundwater of the study area is observed when pH and the bicarbonate concentration are high. Data plotted in Gibbs diagram show that all groundwater samples fall under rock weathering dominance group with a trend towards the evaporation dominance category. An assessment of the chemical composition of groundwater reveals that most of the groundwater samples have compositions of Ca²⁺–Mg²⁺–Cl^? > Ca²⁺–Na⁺–HCO₃ ^? > Ca²⁺–HCO₃ ^? > Na⁺–HCO₃ ^?. This suggests that the characteristics of the groundwater flow regime, long residence time and the extent of groundwater interaction with rocks are the major factors that influence the concentration of fluoride. It is advised not to utilize the groundwater for drinking purpose in the areas delineated, and they should depend on alternate safe source.     

Groundwater flow dynamics in the complex aquifer system of Gidabo River Basin (Ethiopian Rift): a multi-proxy approach

Hydrochemical and isotope data in conjunction with hydraulic head and spring discharge observations were used to characterize the regional groundwater flow dynamics and the role of the tectonic setting in the Gidabo River Basin, Ethiopian Rift. Both groundwater levels and hydrochemical and isotopic data indicate groundwater flow from the major recharge area in the highland and escarpment into deep rift floor aquifers, suggesting a deep regional flow system can be distinguished from the shallow local aquifers. The δ¹⁸O and δ²H values of deep thermal (≥30 °C) groundwater are depleted relative to the shallow (<60 m below ground level) groundwater in the rift floor. Based on the δ¹⁸O values, the thermal groundwater is found to be recharged in the highland around 2,600 m a.s.l. and on average mixed with a proportion of 30 % shallow groundwater. While most groundwater samples display diluted solutions, δ¹³C data of dissolved inorganic carbon reveal that locally the thermal groundwater near fault zones is loaded with mantle CO₂, which enhances silicate weathering and leads to anomalously high total dissolved solids (2,000–2,320 mg/l) and fluoride concentrations (6–15 mg/l) exceeding the recommended guideline value. The faults are generally found to act as complex conduit leaky barrier systems favoring vertical mixing processes. Normal faults dipping to the west appear to facilitate movement of groundwater into deeper aquifers and towards the rift floor, whereas those dipping to the east tend to act as leaky barriers perpendicular to the fault but enable preferential flow parallel to the fault plane.     

Evaluation of hydrogeochemical characteristics of phreatic alluvial aquifers in southeastern coastal belt of Prakasam district, South India

The assessment of hydrogeochemical processes that govern the water quality of inland freshwater aquifers in coastal environment, especially in Indian sub-continent, is occasionally attempted. To bridge the gap, a detail hydrochemical evaluation of groundwater occurring in coastal alluvium is attempted. Single set of high-density water sampling is done from a limited area to gain an in-depth knowledge of the processes that govern the water chemistry of the sandy aquifers. The water is of weak alkaline nature and less mineralized, EC being < 1,000 μS/cm in many samples. Major ion composition indicates that water is contaminated with excess concentration of nitrates. Ionic abundance is in the order of Cl^? > Na⁺  > Ca²⁺ > HCO₃ ^? > SO₄ ^2? > Mg²⁺  > NO₃ ^?. Na⁺ and Cl^? are almost in similar proportions implying the influence of coastal climate on water quality. The water shows modest variation in their ionic assemblage among different sample points as evident from Schoeller scheme. Groundwater can be classified into three distinct facies viz. Cl^?–Ca²⁺–Mg²⁺, Na⁺–Cl^? and Ca²⁺–Mg²⁺–HCO₃ ^? types. The ionic assemblages, their indices, ratios and cross-plots substantiate that multiple processes were involved in the evolution of the water chemistry. Among them, silicate weathering, halite dissolution, ion exchange and base exchange played prominent role in the ion enrichment of groundwater. The aquatic chemistry is further influenced and modified by marine environment, evapotranspiration and anthropogenic inputs which is authenticated by good correlation (r ² = 1) among the Na⁺–Cl^?, EC–Mg²⁺, Na⁺ and Cl^?. Gibbs plots established that evaporation is more responsible for contribution of minerals to the groundwater than aquifer material. Nitrate contamination can be attributed for poor sewerage disposal mechanism which is aggravated by fertilizer inputs, irrigation practices and agriculture activity. A contrasting correlation (r ² ≥90 to <0.40) among select pairs of ions reassures dissimilar source of those ions, involvement of multiple processes and limited interaction of formation water with aquifer material.     

The evolution of groundwater in the Tyrrell catchment, south-central Murray Basin, Victoria, Australia

The Tyrell catchment lies on the western margin of the Riverine Province in the south-central Murray Basin, one of Australia’s most important groundwater resources. Groundwater from the shallow, unconfined Pliocene Sands aquifer and the underlying Renmark Group aquifer is saline (total dissolved solids up to 150,000 mg/L) and is Na-Cl-Mg type. There is no systematic change in salinity along hydraulic gradients implying that the aquifers are hydraulically connected and mixing during vertical flow is important. Stable isotopes (¹⁸O+²H) and Cl/Br ratios indicate that groundwater is entirely of meteoric origin and salts in this system have largely been derived by evapotranspiration of rainfall with only minor halite dissolution, rock weathering (mainly feldspar dissolution), and ion exchange between Na and Mg on clays. Similarity in chemistry of all groundwater in the catchment implies relative consistency in processes over time, independent of any climatic variation. Groundwater in both the Pliocene Sands and Renmark Group aquifers yield ages of up to 25 ka. The Tyrrell Catchment is arid to semi-arid and has low topography. This has resulted in relatively low recharge rates and hydraulic gradients that have resulted in long groundwater residence times.     

Groundwater mixing in the discharge area of San Vittorino Plain (Central Italy): geochemical characterization and implication for drinking uses

Discharge areas of carbonate fractured and karstified aquifers are a sensitive system of great interest, where frequently groundwater resources are tapped for drinking water supply. In geological settings affected by recent and/or active tectonics, mixing between fresh water coming from recharge areas and groundwater from deeper circuits, influenced by raising fluids, influences hydrogeochemistry. Surveys on major ions, trace elements and stable isotopes have been performed in the San Vittorino Plain (Central Italy), where the major source of drinking water for Rome is located (Peschiera Springs, mean discharge 18 m³ s^?1, half of them tapped). Results of 21 springs revealed different contribution from recharge areas and deep flow paths, by increasing salinity and ion content, with particular references to Ca²⁺, HCO₃ ^? and SO₄ ^2?. Three main groups, respectively, related to fresh waters from recharge areas, groundwater from deep contribution and a mixing group between them, have been identified. Water stable isotopes allow to identify the common origin from rainfall and a very steady contribution with seasons and year, due to the huge extent of recharge area (>1000 km²). Saturation Indexes gave insight on the contribution of deep fluids, mainly CO₂ and H₂S, which turned groundwater to undersaturated conditions, facilitating rock dissolution. By PHREEQC software, the mixing between two considered end-members has been simulated, evaluating about 25% of deep contribution in the basal springs of San Vittorino Plain. Chemistry of Peschiera spring reveals a very limited percentage of deep flow paths (10%), which can lead to slight hydrochemistry changes even in possible drought conditions, when discharge can decrease until 15 m³ s^?1.     

Hydrogeochemical characterization and evolution of a regional karst aquifer in the Cuatrociénegas area,Mexico

The Cuatrociénegas area is useful for the investigation of the effect of groundwater extraction in the Chihuahuan freshwater xeric ecoregion. It has been investigated at this time using a selection of geochemical indicators (major, minor and trace elements) and δ³⁴S data, to characterize the origin of groundwater, the main geochemical processes and the mineral/groundwater interactions controlling the baseline geochemistry. The area is composed of limestones of Mesozoic age, with a composite thickness of about 500 m, overlaid by basin fill (poorly consolidated young sediments). Substantial water extraction and modification of natural discharges from the area along the last century have produced a detrimental impact on ecosystem structure and function. Water–rock interactions, mixing and evaporative processes dominate the baseline groundwater quality. Natural recharge is HCO₃–Ca type in equilibrium with calcite, low salinity (TDS?<?500 mg/L), Cl^? lower than 11 mg/L and average Li⁺ concentration of 0.005 mg/L. Along the groundwater flow systems, δ³⁴S evidence and mass transfer calculations indicate that Cretaceous gypsum dissolution and dedolomitization reactions adjust water composition to the SO₄–Ca type. The increase of water–rock interaction is reflected by Cl^? values increase (average 68 mg/L), TDS up to about 1500 mg/L and an average Li⁺ concentration of 0.063 mg/L. Calculations with chemical geothermometers indicate that temperature at depth could be at maximum of 15–20 °C higher than field-measured temperature for pozas. After groundwater is discharged to the surface, chemical evolution continues; water evaporation, CO₂ degassing and precipitation of minerals such as gypsum, calcite and kaolinite represent the final processes and reactions controlling water chemical composition.     

Groundwater flow dynamics of weathered hard-rock aquifers under climate-change conditions: an illustrative example of numerical modeling through the equivalent porous media approach in the north-western Pyrenees (France)

A numerical groundwater model of the weathered crystalline aquifer of Ursuya (a major water source for the north-western Pyrenees region, south-western France) has been computed based on monitoring of hydrological, hydrodynamic and meteorological parameters over 3 years. The equivalent porous media model was used to simulate groundwater flow in the different layers of the weathered profile: from surface to depth, the weathered layer (5?·?10^?8?≤?K?≤?5?·? 10^?7 m s^?1), the transition layer (7?·?10^?8?≤?K?≤?1?·? 10^?5 m s^?1, the highest values being along major discontinuities), two fissured layers (3.5?·?10^?8?≤?K?≤?5?·?? 10^?4 m s^?1, depending on weathering profile conditions and on the existence of active fractures), and the hard-rock basement simulated with a negligible hydraulic conductivity (K = 1 10 ^?9 ). Hydrodynamic properties of these five calculation layers demonstrate both the impact of the weathering degree and of the discontinuities on the groundwater flow. The great agreement between simulated and observed hydraulic conditions allowed for validation of the methodology and its proposed use for application on analogous aquifers. With the aim of long-term management of this strategic aquifer, the model was then used to evaluate the impact of climate change on the groundwater resource. The simulations performed according to the most pessimistic climatic scenario until 2050 show a low sensitivity of the aquifer. The decreasing trend of the natural discharge is estimated at about ?360 m³ y^?1 for recharge decreasing at about ?5.6 mm y^?1 (0.8 % of annual recharge).     

Hydrochemistry and isotopic studies to identify Ganges River and riverbank groundwater interaction, southern Bangladesh

The Ganges River water and riverbank shallow groundwater were studied during a single wet season using the hydrochemical and isotopic composition of its dissolved load. The dissolved concentrations of major ions (Cl^?, SO₄ ^2?, NO₃ ^?, HCO₃ ^?, Ca²⁺, Na⁺, Mg²⁺, and K⁺), trace elements (barium (Ba) and strontium (Sr)) and stable isotopes (O and D) were determined on samples collected from the Ganges River and its riverbank shallow aquifers. In the present study, the shallow groundwater differs significantly from the Ganges River water; it shows distinct high concentrations of Ca²⁺, Mg²⁺, HCO₃ ^?, Ba, and Sr due to water–rock interaction and this in particular suggests that the Ganges River may not contribute significantly to the riverbank shallow aquifers during wet season. Besides, the sum of the total cationic charge (∑⁺, in milliequivalents per liter) in the groundwater shows high values (2.48 to 13.91 meq/L, average 9.12 meq/L), which is much higher than the sum of the cations observed in the Ganges water (1.36 to 3.10 meq/L, average 1.94 meq/L). Finally, the more depleted stable isotopic (δ ¹⁸O and δ ²H) compositions of the Ganges River water are in contrast to those of the riverbank aquifer having enriched stable isotopic values during the wet season and the riverbank groundwater thus has a purely local origin from precipitation.     

Hydrochemical and isotopic investigation of groundwater of Al-Batin alluvial fan aquifer,Southern Iraq

Major ions and important trace elements in addition to δ¹⁸O and δ²H were analysed for 43 groundwater samples sampled from the Al-Batin alluvial fan aquifer, South Iraq. The most dominant ions (with respect to molarity) were: Na⁺ > Cl^? > SO₄ ^2? > Ca²⁺ > Mg²⁺ > NO₃ ^? > HCO₃ ^?, with total dissolved solids (TDS) averaging 7855 mg/L. High concentrations were found for the trace elements U, Mo, V, B, Sr, and Cr. This study suggests a hydraulic connection exists near the fan apex between the uppermost part of the Al-Batin aquifer and the underlying Dammam aquifer by means of the Abu-Jir fault system. Except for the effects of extensive irrigation, fertilizer use, and poorly maintained sewers, the groundwater chemistry is mainly controlled by geological processes such as dissolution of evaporites and the enrichment of dissolved ions as a result of the high evaporation and low recharge rate. Furthermore, it is shown that the Kuwaiti fuel–oil burning during Gulf War in 1991 contributed to the enrichment of V and Mo in the studied aquifer. The spatial distribution of most ions appears to generally increase from the south-west towards the north-east, in the direction of groundwater flow. The stable isotopes show heavier values in groundwater with a gradually increasing trend in the direction of groundwater flow due to the decreasing depth to groundwater and thus increasing of evaporation from both groundwater or irrigation return water. Additionally, the stable isotope signature suggests that rainfall from sources in the Arabian Gulf and the Arabian Sea is the major source of recharge for the Al-Batin aquifer. Except for two samples of groundwater, all samples were not suitable for potable use according to the WHO standards. Most of the groundwater is suitable for some agricultural purpose and for livestock water supply. Apart from the high salinity, boron represents the most critical element in the groundwater with respect to agricultural purposes.     

Isotope Geochemistry of Groundwater from Fractured Dolomite Aquifers in Central Slovenia

The hydrogeochemistry and isotope geochemistry of groundwater from 85 wells in fractured dolomite aquifers of Central Slovenia were investigated. This groundwater represents waters strongly influenced by chemical weathering of dolomite with an average of δ¹³C_CARB value of +2.2 ‰. The major groundwater geochemical composition is HCO₃ ^? > Ca²⁺ > Mg²⁺. Several differences in hydrogeochemical properties among the classes of dolomites were observed when they were divided based on their age and sedimentological properties, with a clear distinction of pure dolomites exhibiting high Mg²⁺/Ca²⁺ ratios and low Na⁺, K⁺ and Si values. Trace element and nutrient concentrations (SO₄ ^2?, NO₃ ^?) were low, implying that karstic and fractured dolomite aquifers are of good quality to be used as tap water. Groundwater was generally slightly oversaturated with respect to calcite and dolomite, and dissolved CO₂ was up to 46 times supersaturated relative to the atmosphere. The isotopic composition of oxygen (δ¹⁸O_H2O), hydrogen (δD_H2O) and tritium ranged from ?10.3 to ?8.4 ‰, from ?68.5 to ?52.7 ‰ and from 3.5 TU to 10.5 TU, respectively. δ¹⁸O and δD values fell between the GMWL (Global Meteoric Water Line) and the MMWL (Mediterranean Meteoric Water Line) and indicate recharge from precipitation with little evaporation. The tritium activity in groundwater suggests that groundwater is generally younger than 50 years. δ¹³C_DIC values ranged from ?14.6 to ?9.3 ‰ and indicated groundwater with a contribution of degraded organic matter/dissolved inorganic carbon in the aquifer. The mass balances for groundwater interacting with carbonate rocks suggested that carbonate dissolution contributes from 43.7 to 65.4 % and degradation of organic matter from 34.6 to 56.3 %.     

Hydrogeochemical and isotopic evolution of water in the Complexe Terminal aquifer in the Algerian Sahara

The hydrogeochemical and isotopic evolution of groundwaters in the Mio–Pliocene sands of the Complexe Terminal (CT) aquifer in central Algeria are described. The CT aquifer is located in the large sedimentary basin of the Great Oriental Erg. Down-gradient groundwater evolution is considered along the main representative aquifer cross section (south–north), from the southern recharge area (Tinrhert Plateau and Great Oriental Erg) over about 700 km. Groundwater mineralisation increases along the flow line, from 1.5 to 8 g l^?1, primarily as a result of dissolution of evaporite minerals, as shown by Br/Cl and strontium isotope ratios. Trends in both major and trace elements demonstrate a progressive evolution along the flow path. Redox reactions are important and the persistence of oxidising conditions favours the increase in some trace elements (e.g. Cr) and also NO₃ ^?, which reaches concentrations of 16.8 mg l^?1 NO₃-N. The range in ¹⁴C, 0–8.4 pmc in the deeper groundwaters, corresponds with late Pleistocene recharge, although there then follows a hiatus in the data with no results in the range 10–20 pmc, interpreted as a gap in recharge coincident with hyper-arid but cool conditions across the Sahara; groundwater in the range 24.7–38.9 pmc signifies a distinct period of Holocene recharge. All δ¹⁸O compositions are enriched relative to deuterium and are considered to be derived by evaporative enrichment from a parent rainfall around ?11‰ δ¹⁸O, signifying cooler conditions in the late Pleistocene and possibly heavy monsoon rains during the Holocene.     

Groundwaters of the Central Ethiopian Rift: diagnostic trends in trace elements, δ<Superscript>18</Superscript>O and major elements

The Ethiopian Rift (a major portion of the Great East African Rift) is characterized by a narrow elongated depression bounded by highlands from both sides. This topographic configuration leads to a monsoon redistribution which resulted in an arid rift floor and humid high rainfall highlands. The rifting and associated volcanism also caused a thinning of the crust and facilitates influx of CO₂ and other mantle gases as diffuse sources or along faults from deeper sources. Groundwaters in the rift floor are usually of high mineral content (high F, U, As and salinity) while those on the plateau are of low mineral content. Among many factors, groundwater availability and quality in the rift floor aquifers is the function of their connection to the aquifers in the high rainfall plateau and the residence time of groundwater prior to reaching the rift floor. This entails the need for addressing one basic hydrologic question in such a setting: at what depth and rate does recharge from the high rainfall highland reach the lowland rift aquifers? This study uses spatial variations in trace elements and relates them to ¹⁴C variations, thereby investigating the suitability of using trace elements as proxies for residence time estimation of groundwaters of relatively short (1,000–2,000 years) residence time. This work also investigates the behavior of trace element trends along the groundwater flow path in a rifted setting and compares them with such trends in sedimentary aquifers elsewhere. The comparison shows a clear difference in behavior of trace elements along the groundwater flow path when compared with such variations in big sedimentary basins with no prominent rifting and volcanism, suggesting the need of calibrating the relation between trace elements and any direct residence time indicators. An integrated use of major elements, trace elements, and environmental isotopes reveals that the main recharge of the aquifers originates from mountain blocks and that recharge takes place via fractures with no evidence of evaporation prior to recharge. Redox processes appear to play a limited role in trace element geochemistry of groundwaters in the region. Progressive trends in trace element composition along the groundwater flow path suggest continuous groundwater flow from the plateau.     

Geochemical characteristics and controlling factors of chemical composition of groundwater in a part of Guntur district,Andhra Pradesh,India

A survey on quality of groundwater was carried out for assessing the geochemical characteristics and controlling factors of chemical composition of groundwater in a part of Guntur district, Andhra Pradesh, India, where the area is underlain by Peninsular Gneissic Complex. The results of the groundwater chemistry show a variation in pH, EC, TDS, Ca²⁺, Mg²⁺, Na⁺, K⁺, HCO₃ ^?, Cl^?, SO₄ ^2?, NO₃ ^? and F^?. The chemical composition of groundwater is mainly characterized by Na⁺?HCO₃ ^? facies. Hydrogeochemical type transits from Na⁺–Cl^?–HCO₃ ^? to Na⁺–HCO₃ ^?–Cl^? along the flow path. Graphical and binary diagrams, correlation coefficients and saturation indices clearly explain that the chemical composition of groundwater is mainly controlled by geogenic processes (rock weathering, mineral dissolution, ion exchange and evaporation) and anthropogenic sources (irrigation return flow, wastewater, agrochemicals and constructional activities). The principal component (PC) analysis transforms the chemical variables into four PCs, which account for 87% of the total variance of the groundwater chemistry. The PC I has high positive loadings of pH, HCO₃ ^?, NO₃ ^?, K⁺, Mg²⁺ and F^?, attributing to mineral weathering and dissolution, and agrochemicals (nitrogen, phosphate and potash fertilizers). The PC II loadings are highly positive for Na⁺, TDS, Cl^? and F^?, representing the rock weathering, mineral dissolution, ion exchange, evaporation, irrigation return flow and phosphate fertilizers. The PC III shows high loading of Ca²⁺, which is caused by mineral weathering and dissolution, and constructional activities. The PC IV has high positive loading of Mg²⁺ and SO₄ ^2?, measuring the mineral weathering and dissolution, and soil amendments. The spatial distribution of PC scores explains that the geogenic processes are the primary contributors and man-made activities are the secondary factors responsible for modifications of groundwater chemistry. Further, geochemical modeling of groundwater also clearly confirms the water–rock interactions with respect to the phases of calcite, dolomite, fluorite, halite, gypsum, K-feldspar, albite and CO₂, which are the prime factors controlling the chemistry of groundwater, while the rate of reaction and intensity are influenced by climate and anthropogenic activities. The study helps as baseline information to assess the sources of factors controlling the chemical composition of groundwater and also in enhancing the groundwater quality management.     

Identifying interactions between river water and groundwater in the North China Plain using multiple tracers

Interactions between river water and groundwater have been used to help understand the movement of water and to evaluate water quality in the semi-arid area of the North China Plain (NCP). Stable isotopes, chlorofluorocarbons (CFCs) and hydrochemistry were used to study the influence of surface water from the Xiao River on regional groundwater. Using a mass balance approach based on chloride concentrations, hydrogen and oxygen isotope ratios, the average fraction of surface water recharging to groundwater was 50–60 %. CFC results indicated that the groundwater recharge age varied from 22.5 to 39.5 years. The vertical flow velocity of groundwater was estimated at about 1.8–3.5 m year^?1. Nitrate concentrations in groundwater varied from 9.42 to 156.62 mg L^?1, and exceeded 50 mg L^?1 in most aquifers shallower than 80 m bordering the Xiao River. The δ ¹⁵N-NO₃ data indicate that the major sources of nitrogen in groundwater are human sewage and animal excreta. Because groundwater is the main source of drinking water, there should be concern about public health related to the elevated nitrate concentrations in the NCP.     

Dévitrification et altération supergène d'une rhyolite (bassin du Paraná, Brésil) : mécanismes et bilans géochimiques

The weathering of a rhyolitic lava flow of the Paraná Basin (Brazil) developed, on few centimeters only, simplified petrographic features. The initial meteoric fluid pass-way is marked by celadonite-to-nontronite transformation. The second step is the complete dissolution of plagioclases, and the last one is the massive precipitation of halloysite. The geochemical mass balances according to the alteration features demonstrate the progressive leaching of major and trace elements fractionated by plagioclases, glass and opaques, and the sorption of Cu>As>Sb in the halloysite matrix. To cite this article: M. Bernard et al., C. R. Geoscience 336 (2004).     

Dissolved noble gases and stable isotopes as tracers of preferential fluid flow along faults in the Lower Rhine Embayment,Germany

Groundwater in shallow unconsolidated sedimentary aquifers close to the Bornheim fault in the Lower Rhine Embayment (LRE), Germany, has relatively low δ²H and δ¹⁸O values in comparison to regional modern groundwater recharge, and ⁴He concentrations up to 1.7?×?10^?4 cm³ (STP) g^–1?±?2.2 % which is approximately four orders of magnitude higher than expected due to solubility equilibrium with the atmosphere. Groundwater age dating based on estimated in situ production and terrigenic flux of helium provides a groundwater residence time of ～10⁷ years. Although fluid exchange between the deep basal aquifer system and the upper aquifer layers is generally impeded by confining clay layers and lignite, this study’s geochemical data suggest, for the first time, that deep circulating fluids penetrate shallow aquifers in the locality of fault zones, implying  that sub-vertical fluid flow occurs along faults in the LRE. However, large hydraulic-head gradients observed across many faults suggest that they act as barriers to lateral groundwater flow. Therefore, the geochemical data reported here also substantiate a conduit-barrier model of fault-zone hydrogeology in unconsolidated sedimentary deposits, as well as corroborating the concept that faults in unconsolidated aquifer systems can act as loci for hydraulic connectivity between deep and shallow aquifers. The implications of fluid flow along faults in sedimentary basins worldwide are far reaching and of particular concern for carbon capture and storage (CCS) programmes, impacts of deep shale gas recovery for shallow groundwater aquifers, and nuclear waste storage sites where fault zones could act as potential leakage pathways for hazardous fluids.     

A comparative study of aquifer systems occurring at the Paraná sedimentary basin, Brazil: U-isotopes contribution

The radioactivity due to ²³⁸U and ²³⁴U in three aquifer systems occurring within the Paraná sedimentary basin, South America, has been investigated. Uranium is much less dissolved from fractured igneous rocks than from the porous sedimentary rocks as indicated by the U-mobility coefficients between 7.6 × 10^?6 and 1.2 × 10^?3 g cm^?3. These values are also compatible with the U preference ratios relative to Na, K, Ca, Mg and SiO₂, which showed that U is never preferentially mobilized in the liquid phase during the flow occurring in cracks, fissures, fractures and faults of the igneous basaltic rocks. Experimental dissolution of diabase grains on a time-scale laboratory has demonstrated that the U dissolution appeared to be a two-stage process characterized by linear and second-order kinetics. The U dissolution rate was 8 × 10^?16 mol m^?2 s^?1 that is within the range of 4 × 10^?16–3 × 10^?14 mol m^?2 s^?1 estimated for other rock types. The ²³⁴U/²³⁸U activity ratio of dissolved U in solutions was higher than unity, a typical result expected during the water–rock interactions when preferential ²³⁴U-leach from the rock surfaces takes place. Some U-isotopes data allowed estimating 320 ka for the groundwater residence time in a sector of a transect in São Paulo State. A modeling has been also realized considering all U-isotopes data obtained in Bauru (35 samples), Serra Geral (16 samples) and Guarani (29 samples) aquifers. The results indicated that the Bauru aquifer waters may result from the admixture of waters from Guarani (1.5 %) and Serra Geral (98.5 %) aquifers.