Hydrochemistry deducing basaltic trap thickness for groundwater resource mapping along the Deccan Volcanic Province (DVP) margin in India

It is hypothesized that hydrochemical parameters can be employed to deduce the basaltic trap thickness and that there exist diverse hydrochemical processes within the existing host rocks along the Deccan Volcanic Province (DVP) margin. Chemical imprints of aquifers, in various flows of flood basalt and fissured zones of granites, had been appraised using major ion chemistry of groundwater in a test site of 623 km² at the southern margin of the DVP in India. The wide ranging hydrochemical processes, obtained from empirical data, describe the predominance of carbonate, dolomite, calcite and anorthite weathering in basalts, and alkali feldspar (albite and orthoclase) in granites. Results showed that the elevated concentrations of alkaline earth elements in basaltic aquifers and alkali rich elements in granitic aquifers were useful in tracing the sources of host rock for dissolved mineral reactants. Further, a digital elevation model using Shuttle Radar Topography Mission (90 m) elevation satellite data aided in deciphering trap thickness, vertical transition zone of trap and granitic basement comprising the well depths and hydrochemistry. The mapping of trap thickness is useful to explore the groundwater resources at the vertical transition zone between the basaltic trap and granitic base. The estimated thickness of the basaltic trap is varied from 4 to 98 m at the DVP southern margin, which is further verified with the help of exploratory well lithologs matched closely.     

Study on the dynamic characteristics of groundwater in the valley plain of Lhasa City

The valley plain of Lhasa City is located on the Qinghai-Tibetan Plateau, which is one of the most developed and densely populated areas in Tibet. Groundwater is an important water supply source and plays an irreplaceable role in the social and economic development of Lhasa City. This study has investigated the dynamic characteristics of groundwater in the valley plain of Lhasa City through the methods of mathematical statistics and hydrochemical analysis. The results showed that local topography, climate, and urbanization substantially influenced the groundwater dynamics. Under the combined influences from urbanization and climate, the groundwater level decreased over three time periods, but the groundwater-level configuration has not shown significant changes in over 15 years. From 1997 to 2015, the hydrochemical type of groundwater has changed from HCO₃–Ca to HCO₃·SO₄–Ca·Mg and HCO₃·SO₄–Ca. The concentrations of Cl^?, Mg²⁺, and SO₄^2? in groundwater increased, but the concentrations of other ions were relatively stable. Water–rock interaction was the main mechanism controlling the groundwater chemistry in the study area, and it was mainly associated with the dissolution of silicate, carbonate, and halite.     

Principal component and multivariate statistical approach for evaluation of hydrochemical characterization of fluoride-rich groundwater of Shaslar Vagu watershed,Nalgonda District,India

In order to assess the impact of fluoride-rich groundwater of Shasilair Vagu watershed on groundwater regime, more than hundred groundwater samples for pre- and post-monsoon seasons were collected from bore wells/dug wells and analyzed for major ions. Water quality analysis of major ion chemistry shows elevated concentration of fluoride in groundwater samples. The fluoride concentration ranges from 1.4 to 5.9 mg/l and 1.5 to 5.8 mg/l in pre- and post-monsoons, respectively. The result clearly shows that the seasonal variation of fluoride in groundwater is due to recharge of rain water during monsoon. The water quality data was analyzed by hydrochemical facies (Piper diagram), Gibbs plot, and various plots. Plots of Na versus Cl, Ca versus SO₄, and (Na+Cl)-(SO₄+HCO₃) versus (Na+K-Cl) shows positive and negative values, indicating that their source of high concentration are aquifer, evapotranpiration, and other anthropogenic sources. Saturation index of halite and gypsum shows that all groundwater samples were undersaturated and suggests that carbonate minerals influence the concentration. Using multivariate statistical techniques, viz., principal component (factor analysis and cluster analysis), the analysis brought out impact of intensity of excess use of fertilizers and excess withdrawal of groundwater regime. Multivariate statistical techniques are potential tools and provide greater precision for identifying contaminant parameter linkages.     

Ion chemistry of groundwater and the possible controls within Lhasa River Basin,SW Tibetan Plateau

In order to study the major ion chemistry and controls of groundwater, 65 groundwater samples were collected and their major ions measured from wells within Lhasa River Basin. Groundwater has the characteristics of slightly alkaline and moderate total dissolved solid (TDS). TDS concentration ranged from 122.0 to 489.9 mg/L with a median value of 271.2 mg/L. Almost all the groundwater samples suited for drinking and irrigation. The major cations of groundwater are Ca²⁺ and Mg²⁺, accounting for 59.6 and 31.3% of the cations, respectively. Meanwhile, HCO₃^? and SO₄^2? constituted about 56.7 and 36.9% of the anions, respectively, in Lhasa River Basin. The hydrochemical type of groundwater is HCO₃-SO₄-Ca-Mg. The chemical composition of groundwater samples located in the middle of Gibbs model, which indicates that the major chemical process of groundwater is controlled by rock weathering. Carbonate weathering was the dominant hydro-geochemical process controlling the concentration of major ions in groundwater within Lhasa River Basin, but silicate weathering also plays an important role.     

Drinking quality assessment of some groundwater sources along the stretch of Jhelum River in Kashmir Himalaya

The physicochemical properties and major ion chemistry of the groundwater sources from alluvial aquifers along the stretch (60 km) of Jhelum River in Kashmir Himalaya were determined in order to identify hydro-geochemical processes and their suitability for drinking purposes. The data depicted that calcium and bicarbonates were dominating among the cations and anions. The results indicate the trend of cation dominance as Ca²⁺ > Na⁺ > Mg²⁺ > K⁺, whereas anion dominance was in the order of HCO₃ ^? > Cl^? > SO₄ ^2?. Ratio of calcium to magnesium indicated the dissolution of Ca²⁺ from CaCO₃, which results in an increased levels of Ca²⁺ in the groundwater. Interpretation of Piper Trilinear plot understands the various geochemical processes affecting the groundwater quality and shows groundwater was dominated by Ca–HCO₃ type. The pH was recorded in the slightly alkalinity range 7.2–7.8 and was showing positive correlation with HCO₃ ^?. The chloro-alkaline indices revealed 86% of the sources exchange by a type of base-exchange reactions, rest by cation–anion exchange. Gibbs diagram revealed groundwater sources fall in the category of rock dominance. The concentration of the nitrogen compounds was in the progression of NO₃–N > NH₄–N > NO₂–N, and the PO₄ ^? fluctuated from 0.12 to 0.22 mg/L. Moreover, corrosivity ratio indicated that water from the majority of sources (71%) is safe to supply using pipes without any corrosive effects, while 29% of sources are corrosive in nature and need non-corrosive pipes for transporting and lifting of groundwater. The results revealed, groundwater samples were within permissible limits as prescribed by International and National standards, for drinking purposes. The State government and NGO’s can show their interest in utilizing such water resources to overcome the shortage of drinking water in a sustainable way for the daily consumption of the people living in the vicinity of Jhelum River.     

Impact of pit-toilet leachate on groundwater chemistry and role of vadose zone in removal of nitrate and E. coli pollutants in Kolar District, Karnataka, India

Assessment of chemistry of groundwater infiltrated by pit-toilet leachate and contaminant removal by vadose zone form the focus of this study. The study area is Mulbagal Town in Karnataka State, India. Groundwater level measurements and estimation of unsaturated permeability indicated that the leachate recharged the groundwater inside the town at the rate of 1 m/day. The average nitrate concentration of groundwater inside the town (148 mg/L) was three times larger than the permissible limit (45 mg/L), while the average nitrate concentration of groundwater outside the town (30 mg/L) was below the permissible limit. The groundwater inside the town exhibited E. coli contamination, while groundwater outside the town was free of pathogen contamination. Infiltration of alkalis (Na⁺, K⁺) and strong acids (Cl^?, SO₄ ^2?) caused the mixed Ca–Mg–Cl type (60 %) and Na–Cl type (28 %) facies to predominate groundwater inside the town, while, Ca–HCO₃ (35 %), mixed Ca–Mg–Cl type (35 %) and mixed Ca–Na–HCO₃ type (28 %) facies predominated groundwater outside/periphery of town. Reductions in E. coli and nitrate concentrations with vadose zone thickness indicated its participation in contaminant removal. A 4-m thickness of unsaturated sand + soft, disintegrated weathered rock deposit facilitates the removal of 1 log of E. coli pathogen. The anoxic conditions prevailing in the deeper layers of the vadose zone (>19 m thickness) favor denitrification resulting in lower nitrate concentrations (28–96 mg/L) in deeper water tables (located at depths of ?29 to ?39 m).     

A diagnosis of groundwater quality from a semiarid region in Rajasthan,India

A diagnosis of the groundwater quality of 70 wells sampled during two climatic regimes (dry and raining seasons) from a semiarid area in Rajasthan, India, had been carried out using standard methods. Analysis of the results for various hydrochemical parameters wherein the geological units are alluvium, quartzite and granite gneisses showed that all the parameters did not fall within the World Health Organisation’s acceptable limits for irrigation and drinking water purposes. The order of major cations and anions obtained during the dry and raining seasons are Na⁺ ? Mg²⁺ ? Ca²⁺ ? K⁺ and Cl^?? HCO₃ ^? ? SO₄ ^2?? CO₃ ^?> F^? ? NO₃ ^?, respectively. A maximum value of nitrate of 491.6 mg/l has been examined and its contamination is due to discriminated highly impacted groundwater samples by agricultural activity and small-scale urbanization. Fluoride (F^?) concentration is 6.50 mg/l as a maximum value, whereas values in about 26 % of the samples are more than the permissible limit (1.5 mg/l) for drinking water. The cumulative probability distributions of the selected ions show two individual intersection points with three diverse segments, considered as regional threshold values and highly impacted threshold values for differentiating the samples with the effects of geogenic, anthropogenic and saline water mixing. The first threshold values indicate the background hydrochemical constituents in the study area. The second threshold value of 732 mg/l for bicarbonate indicates that sandy aquifer is being dissolved during wet period, whereas NO₃ ^? concentration of more than the initial threshold value (=75 mg/l) indicates discriminated highly impacted groundwater samples by agricultural activity and urbanization in dry season. Various parameters such as soluble sodium percentage (SSP), salinity (electrical conductivity (EC)), sodium adsorption ratio (SAR), residual sodium carbonate (RSC), Kelley’s ratio (KR), permeability index (PI), residual sodium bicarbonate (RSB) and magnesium absorption ratio (MAR) for the well samples show that, overall, 46 % of groundwater samples are not suitable for irrigation. Further, chloro-alkaline indices (CAIs) were used for distinguishing regional recharge and discharge zones whereas corrosivity ratio (CR) utilized for demarcating areas to use metallic pipes for groundwater supply. In general, groundwater quality is mainly controlled by the chemical weathering of rock-forming minerals. The information obtained represents a base for future work that will help to assess the groundwater condition for periodical monitoring and managing the groundwater from further degradation.     

安徽马鞍山市当涂地区地下水水化学特征及演化机制

【研究目的】 了解长江中下游平原地区地下水流系统并深入分析其地下水水化学特征及其演化机制。【研究方法】 综合马鞍山市当涂地区的水文地质条件、水动力场等,基于研究区水化学基本特征,运用多元统计分析、水化学图件、离子比值和反向水文地球化学模拟等方法对该地区浅层地下水水化学演化进行分析。【研究结果】 结果表明：（1）研究区地下水主要为低矿化度偏碱性水,地下水组分中阳离子以Ca²⁺和Mg²⁺为主,阴离子以HCO₃^-和SO₄^2-为主。（2）研究区地下水水化学类型主要可分为7类,其中松散岩类孔隙含水岩组和碎屑岩类孔隙裂隙含水岩组的水化学类型主要为HCO₃^-Ca型、HCO₃^-Ca·Na型、HCO₃·Cl-Ca·Na型以及HCO₃^-Ca·Mg型;基岩类裂隙含水岩组的化学类型主要为HCO₃·SO₄-Ca·Mg型和SO₄·HCO₃^-Ca·Mg型。（3）研究区浅层地下水水样超标率为46%,总体水质较差,超标率较高的组分依次为Mn、高锰酸盐指数（COD_Mn）、硝酸盐（以N计）、Fe、As、氨氮（以N计）等。（4）研究区地下水的化学组分主要受到岩石风化作用的控制;此外,还存在Na-Ca的正向阳离子交替吸附作用。反向水文地球化学模拟结果进一步定量论证了水岩相互作用对本区浅层地下水组分的形成和演化起着主导作用。【结论】 研究区地下水主要为低矿化度偏碱性,主要可分为松散岩类孔隙水、碎屑岩类孔隙裂隙水和基岩类裂隙水。主要离子比例和反向水文地球化学模拟揭示了本区浅层地下水化学组分主要是地下水溶滤方解石、白云石等碳酸盐矿物、石英、长石等硅酸盐矿物,高岭土等黏土矿物以及岩盐、石膏等达到过饱和之后形成的。     

Hydrogeochemistry and possible sulfate sources in karst groundwater in Chongqing, China

Groundwater from karst subterranean streams is among the world’s most important sources of drinking water supplies, and the hydrochemical characteristics of karst water are affected by both natural environment and people. Therefore, the study of karst groundwater hydrochemistry and its solutes’ sources is very important to ensure the normal function of life support systems. This paper focused on the major ion chemistry and sulfate isotope of karst groundwater in Chongqing for tracing the sulfate sources and related hydrochemical processes. Hydrochemical types of karst groundwater in Chongqing were mainly of the Ca-HCO₃ type or Ca(Mg)-HCO₃ type. However, some hydrochemical types were the K + Na + Ca-SO₄ type (G25 site) or Ca-HCO₃ + SO₄ type (G26 and G14 sites), indicating that the hydrochemistry of these sites may be strongly influenced by anthropogenic activities or unique geological characteristics. The δ³⁴S-SO₄ ^2? of collected karst groundwater sample fell into a range of ?6.8 to 21.5 ‰, with a mean value of 5.6 ‰. In dolomite aquifer, the δ³⁴S-SO₄ ^2? value ranges from ?4.3 to 11.0 ‰, and in limestone aquifer, it ranged from ?6.8 to 21.5 ‰. The groundwater samples from different land use types showed distinctive δ³⁴S-SO₄ ^2? value. The δ³⁴S-SO₄ ^2? value of groundwater samples had range of ?6.8 to 16.7 ‰ (mean 4.0 ‰, n = 11) in cultivated land areas, 1.5–21.5 ‰ (mean 7.2 ‰, n = 20) in forested land areas, and ?4.3 to 0.8 ‰ (mean ?1.7 ‰, n = 2) in coalmine areas. The δ³⁴S-SO₄ ^2? values of groundwater samples collected from factory area and town area were 2.2 and 9.9 ‰, respectively. According to the δ³⁴S information of potential sulfate sources, this paper discussed the possible sulfate sources of collected karst groundwater samples in Chongqing. The variations of both δ³⁴S and 1/SO₄ ^2? values of the groundwater samples indicated that the atmospheric acid deposition (AAD), dissolution of gypsum (GD), oxidation of sulfide mineral (OS) or anthropogenic inputs (SF: sewage or fertilizer) contributed to sulfate in karst groundwater. The influence of oxidation of sulfide mineral, atmospheric acid deposit and anthropogenic inputs to groundwater in Chongqing karst areas was much widespread. For protecting, sustaining, and utilizing the groundwater resources, the sewage possibly originating from urban, mine or industrial area must be controlled and treated, and the use of fertilizer should be limited.     

Hydrochemical characterization of groundwater system of biodiversity experimental field: Jena, Germany

Hydrochemical modeling, graphical methods, and different statistical techniques were applied to understand the nature of geological and hydrochemical processes in a shallow groundwater aquifer of the Jena biodiversity experimental field. Factor and cluster analyses were used to identify the governing underlying processes and to detect the spatial similarity between the sampling points. The hydrochemical modeling, using PHREEQC, was used to interpret the reactive minerals. Results of factor analysis indicated that there are five dominant factors which account for about 90 % of the variance of the chemical dataset in the cold season (March, April, November) and warm season (June, August). Factor analysis showed that 43 % of the variation in the cold season and 53 % of the variation in the warm season of the groundwater hydrochemical data are due to major cations and anions which reveals groundwater-geological matrix interaction. Redox and redox-sensitive elements are the next important factors and account for 15 % and 19 % variation in the cold season and warm season, respectively. The hydrochemical modeling using PHREEQC and X-ray diffraction results showed that calcite, dolomite, quartz, and siderite are reactive minerals and are responsible for changes in chemical composition. The hydrochemical data of the two seasons were also compared and the results showed that the groundwater chemistry of the study area varied seasonally in terms of some parameters such as mainly heavy metals (Ba, B, Fe, Mn, U, V, Zn, Sr, Ni), HCO₃ ^?, and DOC.     

Assessment of shallow groundwater in Lake Nyos catchment (Cameroon,Central-Africa): implications for hydrogeochemical controls and uses

In 1986, carbon dioxide gas exploded from Lake Nyos and killed about 1,800 people. After that disaster, various administrative and research activities have been conducted to mitigate subsequent disasters. However, none of those endeavors have characterized the groundwater chemistry to identify hydrogeochemical processes that control the water chemistry, and the quality of the water for domestic and agricultural uses that support the lives of un-official resettlers around Lake Nyos. Conventional hydrochemical techniques coupled with statistical and graphical analysis were therefore employed to establish the baseline hydrochemical conditions, assess processes controlling solutes distribution in shallow groundwater in the Lake Nyos catchment and explore its usability. Groundwater samples were analyzed for their physical and chemical properties. The wide ranges of electrical conductivity and total dissolved solid values reveal the heterogeneous distribution of groundwater within the watershed. The relative abundance of major dissolved species was Ca > Mg > Na > K for cations and HCO₃ >>> Cl > SO₄ > NO₃ for anions. Piper diagram classified almost all water samples into mixed CaMg–HCO₃ water type. Major ion geochemistry reveals that, in addition to silicates weathering (water–rock interaction), ion exchange processes regulate the groundwater chemistry. Principal component analysis supports the occurrence of water rock interaction. Hierarchical cluster analysis showed that the chemistry of groundwater in the study area is controlled by three main factors, and suggests no hydraulic connectivity between deep lake water and groundwater in the catchment. The quality assessment of the groundwater showed that groundwater parameters are within the acceptable limit of the World Health Organization and Nigeria guidelines for drinking and domestic uses, and water found to be good for irrigation.     

Hydrochemical and isotopic study of groundwater in the Yinchuan plain, China

The Yinchuan plain is located in the arid climate zone of NW China. The western margin of the plain is the Helan mountain connecting a series of normal slip faults. The eastern margin of the plain connects with the Yellow River and adjacents with the Ordos platform. The south of the plain is bordered by the EN fault of the Niushou mountain. The bottom of the plain is the Carboniferous, Permian, or Ordovician rocks. Based on the analysis of groundwater hydrochemical and isotopic indicators, this study aims to identify the groundwater recharge and discharge in the Yinchuan plain, China. The hydrochemical types of the groundwater are HCO₃–SO₄ in the west, HCO₃–Cl in the middle, and Cl–SO₄ in the east. The hydrochemical types are HCO₃–SO₄ in the south, HCO₃–Cl and SO₄–HCO₃ in the middle. The hydrochemical types are complex in the north, mainly SO₄–HCO₃ and Cl–SO₄. Deuterium, ¹⁸O, and tritium values of groundwater indicate that groundwater recharge sources include precipitation, bedrock fissure water, and irrigation return water. Groundwater discharges include evaporation, abstraction, and discharge to surface water. According to the EW isotopic profile, the groundwater flow system (GFS) in the Yinchuan plain can be divided into local flow systems (LFS) and regional flow systems (RFS). Groundwater has lower TDS and higher tritium in the southern Yellow River alluvial plain and groundwater age ranges from 6 to 25 years. The range of groundwater renewal rates is from 11 to 15 % a^?1. The depth of the water cycle is small, and groundwater circulates fast and has high renewal rates. Groundwater has higher TDS and lower tritium in the northern Yellow River alluvial plain. The range of groundwater age is from 45 to 57 years, and renewal rate is from 6 to 0.1 % a^?1. The depth of the water cycle is larger. Groundwater circulates slowly and has low renewal rates.     

Fracture zone-scale variation of trace elements and stable isotopes in calcite in a crystalline rock setting

With an aim to increase the understanding about the isotopic and chemical heterogeneity of calcites in water-conducting fracture zones with different crystalline wall rock compositions at different depths, we present trace element chemistry, isotopic composition (δ¹⁸O, δ¹³C, ⁸⁷Sr/⁸⁶Sr) and biomarkers of euhedral low-temperature fracture-coating calcite. Paleohydrogeological fluctuations and wall rock influence on the hydrochemistry in the deep groundwater are explored. Samples are from several fracture zone sub-fractures (at −360 to −740 m), retrieved during an extensive core drilling campaign in Sweden.Calcite generally showed fracture zone specific values of δ¹³C, δ¹⁸O and ⁸⁷Sr/⁸⁶Sr, which indicates precipitation from relatively homogeneous fluid (similar to the modern groundwater at the site) at the same event in each fracture zone. δ¹⁸O and δ¹³C in the different fracture zones were consistent with precipitation from waters of different salinity and decreasing organic input with depth, respectively. The latter is also supported by biomarkers showing clear indications of SRB-related organic compounds (e.g. iso- and anteiso-C_17:0-branched fatty acids), except in the deepest zone. In contrast to the isotopes, variation in trace elements within the fracture zones was generally up to several orders of magnitude. Manganese and REE, as oppose to the other metals, were higher in the shallow fracture zones (112–1130 and 44–97 ppm, respectively) than in the deeper (28–272 and 5–11 ppm, respectively), in agreement with the groundwater composition. Although the rock types varied between and within the different fracture zones, this had insignificant influence on the trace element chemistry of the calcites. Co-variation was generally relatively large for many trace elements, with isometric logratio correlation generally better than 0.75, which indicates that their variation in the calcites is due to variation of Ca in the fracture water, but other local factors, especially uptake in co-precipitating minerals (clay minerals, barite, pyrite and zeolites), but also microbial activity and metal speciation may have influenced the metal incorporation into calcite. These detailed studies of fracture calcite are of importance for the understanding of variation in fluid chemistry and trace metal uptake in fracture zones, adding together with hydrochemical studies detailed information optimal for site characterisation.     

Identifying key hydrochemical processes in a confined aquifer of an arid basin using multivariate statistical analysis and inverse modeling

Tertiary fractured permeable confined aquifer, which covered about 70 % of the studying area, played an important role in alleviating drinking water shortages. However, about 58 and 79 % of the groundwater samples exceeded the desirable limits for fluoride (1.5 mg/L) and TDS (1,000 mg/L). Two multivariate statistical methods, hierarchical cluster analysis (HCA) and principal components analysis (PCA), were applied to a subgroup of the dataset in terms of their usefulness for groundwater classification, as well as to identify the key processes controlling groundwater geochemistry. In the PCA, two principal factors have been extracted, which could explain 73 % of the total data variability. Among them, factor 1 revealed the source of groundwater salinity and factor 2 explained the elevated fluoride. Two major groups were classified by HCA and Group 1 was near the groundwater recharge zone and Group 2 was mainly distributed over the groundwater discharge zone. Inverse modeling (NETPATH) results indicated that the hydrochemical evolution was primarily controlled by (1) the dissolution of mirabilite, gypsum and halite for the source of groundwater salinity; (2) the release of the adsorbed fluoride through desorption or through competition with HCO₃ ^? under alkalinity condition for the elevated fluoride in the groundwater.     

Characteristics of stable isotope and hydrochemistry of the groundwater around Qinghai Lake, NE Qinghai-Tibet Plateau, China

The integrated use of isotopic and hydrochemical tracers is an effective approach for investigating complex hydrological processes of groundwater. The stable isotope composition and hydrochemistry of the groundwater around Qinghai Lake were investigated to study the sources and recharge areas. Most of the groundwater points lie close to the local meteoric water line, indicating that the ground waters were recharged primarily from precipitation in the basin, though it had undergone varying degrees of evaporation. The hydrochemical analysis showed that the groundwater was mainly freshwater and that the hydrochemical type was Ca–Mg–HCO₃; the results of the boomerang envelope model and solutes calculated indicated that the groundwater chemistry was mainly controlled by carbonate dissolution around Qinghai Lake. The recharge altitudes of groundwater were relatively low (at 3,400 m.a.s.l) on the northern shore of Qinghai Lake (locations G1 and G5), relatively high (above 3,900 m.a.s.l) on the southern shore (locations G3 and G4), and approximately 3,700 m.a.s.l on the western shore (location G2). Furthermore, groundwater samples from the fault zone (e.g., G3) would be recharged in part from fissure or inter-basin water. High salinity of groundwater on the western shore (location G2) was related with the evaporite dissolution, the groundwater is unsuitable for drinking, and the drinking water should be improved and enhanced in this area. Knowledge of our research can promote effective management of water resources in this cold and semiarid region and add new data to global groundwater database.     

Hydrochemical and isotopic characteristics of groundwater in the Ndop plain,northwest Cameroon: resilience to seasonal climatic changes

Shallow groundwater (>30 mbgl) is an essential source of drinking water to rural communities in the Ndop plain, northwest Cameroon. As a contribution to water management, the effect of seasonal variation on the groundwater chemistry, hydrochemical controls, drinking quality and recharge were investigated during the peaks of the dry (January) and rainy (September) seasons. Field measurements of physical parameters were preceded by sampling 58 groundwater samples during both seasons for major ions and stable isotope analyses. The groundwater, which was barely acidic (mean pH of 6) and less mineralised (TDS < 272 mg/l), showed no significant seasonal variation in temperature, pH and TDS during the two seasons. The order of cation abundance (meq/l) was Na⁺ > Ca²⁺ > Mg²⁺ > K⁺ and Na⁺ > Mg²⁺ > Ca²⁺ > K⁺ in the dry and rainy seasons, respectively, but that of anions ( \( {\text{HCO}}_{3}^{ - } \)  >  \( {\text{NO}}_{3}^{ - } \)  > Cl^? >  \( {\text{SO}}_{4}^{2 - } \)  > F^?) was similar in both seasons. This suggests a negligible effect of seasonal variations on groundwater chemistry. The groundwater, which was CaMgHCO₃ and NaHCO₃, is chemically evolved rainfall (CaMgSO₄Cl) in the area. Silicate mineral dissolution and cation-exchange were the main controls on groundwater chemistry while there was little anthropogenic influence. The major ions and TDS concentrations classified the water as suitable for human consumption as per WHO guidelines. The narrow cluster of δ¹⁸O and δD of same groundwater from both seasons between the δ¹⁸O and δD values of May–June precipitation along the Ndop Meteoric Water Line indicates meteoric origin, rapid recharge (after precipitation) and timing of recharge between May and June rainfall. Diffuse groundwater recharge mainly occurs at low altitudes (<1,400 m asl) within the plain. Besides major ions and TDS, the similar δ¹⁸O and δD of groundwater from both seasons indicate a consistent groundwater recharge and flow pattern throughout the year and resilience to present day short-term seasonal climatic variations. However, controlled groundwater abstraction is recommended given the increasing demand.     

Hydrogeochemical characterization and quality assessment of groundwater around Umrer coal mine area Nagpur District,Maharashtra, India

Quality assessment as well as hydrogeochemical characterization of 45 representative groundwater samples around Umrer coal mine area was undertaken. The pH of the water lies in the normal range i.e. from 7.5 to 8.5, the electrical conductivity varies from 826 to 1,741, the total hardness varies from 289 to 1,302 and the TDS values range from 528.6 to 1,114.2 mg/l which reflects variation in lithology and thus, the distinction in hydrogeological regime. The cation chemistry is dominated by Ca²⁺ and Mg²⁺ while anion chemistry is dominated by Cl^? and HCO₃ ^?. Out of total ten hydrochemical facies, the two dominant facies are Mg–Ca–HCO₃ (37.7 %) and Ca–Mg–SO₄–HCO₃ (17.7 %). The groundwater in the study area, in general, is useful for drinking and domestic use; however, it has marginal utility for irrigation purpose. Standard US Salinity Laboratory classification shows that water of the study area belongs to C2–S1 and C3–S1 classes. The concentration of 9 trace elements analysed from 18 samples did not exceed the desirable limit.     

Groundwater Evolution and Mineral Alteration Reactions in the Basaltic Rock Sequence of Mt. Wasserkuppe, Germany: A Case Study

Groundwater sampling was accomplished in the basaltic sequence of the Rh?n mountain range, Germany, in order to investigate hydrochemical groundwater evolution and to delineate mineral alteration reactions involved in natural weathering. The hydrochemical compositions of near-surface groundwaters indicate a Ca/Mg–HCO₃ type with near-neutral pH and evolve to a Na–HCO₃ type with high pH at greater depth. Column experiments were performed with basaltic and phonolitic rock samples to determine individual mineral alteration reactions. The basic reactions could be related to the alteration of olivine, Ca-pyroxene, plagioclase, pyrrhotite, and feldspathoids under formation of secondary clay minerals (smectites, illite) and goethite. The mineral alteration reactions deduced from the leaching experiments by inverse modelling were found to be consistent with the mineral reactions associated with the natural groundwaters. The reactions calculated for groundwater evolution involve the alteration of primary and secondary minerals to produce low-T mineral phase. The conversion of secondary Na-beidellite to illite occurs at a later stage of groundwater evolution, reducing the concentrations of K⁺ and Mg²⁺. Near-surface groundwaters do not indicate significant cation exchange. Initial cation exchange requires elevated pH values, with Mg²⁺ removed from solution preferred to Ca²⁺. Na-alkalisation of the groundwaters at greater depth suggests the exchange of Na⁺ for Mg²⁺ and Ca²⁺ on Na-beidellite, supported by cation exchange on coatings of iron hydroxides as alteration products. Among the mature high-pH groundwater at greater depth, the dissolution of anorthite and albite has significant effect on groundwater composition.     

Dynamics of greenhouse gases in the river–groundwater interface in a gaining river stretch (Triffoy catchment,Belgium)

This study investigates the occurrence of greenhouse gases (GHGs) and the role of groundwater as an indirect pathway of GHG emissions into surface waters in a gaining stretch of the Triffoy River agricultural catchment (Belgium). To this end, nitrous oxide (N₂O), methane (CH₄) and carbon dioxide (CO₂) concentrations, the stable isotopes of nitrate, and major ions were monitored in river and groundwater over 8 months. Results indicated that groundwater was strongly oversaturated in N₂O and CO₂ with respect to atmospheric equilibrium (50.1 vs. 0.55 μg L^?1 for N₂O and 14,569 vs. 400 ppm for CO₂), but only marginally for CH₄ (0.45 vs. 0.056 μg L^?1), suggesting that groundwater can be a source of these GHGs to the atmosphere. Nitrification seemed to be the main process for the accumulation of N₂O in groundwater. Oxic conditions prevailing in the aquifer were not prone for the accumulation of CH₄. In fact, the emissions of CH₄ from the river were one to two orders of magnitude higher than the inputs from groundwater, meaning that CH₄ emissions from the river were due to CH₄ in-situ production in riverbed or riparian zone sediments. For CO₂ and N₂O, average emissions from groundwater were 1.5?×?10⁵ kg CO₂ ha^?1 year^?1 and 207 kg N₂O ha^?1 year^?1, respectively. Groundwater is probably an important source of N₂O and CO₂ in gaining streams but when the measures are scaled at catchment scale, these fluxes are probably relatively modest. Nevertheless, their quantification would better constrain nitrogen and carbon budgets in natural systems.     

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

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