Hydrochemical evolution and water quality along the groundwater flow path in the Sandıklı plain, Afyon, Turkey

 An unconfined aquifer system suggests an open system in the study area. Hydrochemical evolution is related to the flow path of groundwater. The groundwaters are divided into two hydrochemical facies in the study area, 1) Ca–Mg–HCO₃ and 2) Ca–Mg–SO₄HCO₃. Facies 1 has shallow (young) waters which dominate in recharge areas during rapid flow conditions, whereas facies 2 may show shallow and mixed waters which dominate intermediate or discharge areas during low flow conditions. Ionic concentrations, TDS, EC and water quality are related to groundwater residence time and groundwater types. The groundwaters in the plain are chemically potable and suitable for both domestic and agricultural purposes. Received: 20 May 1996 · Accepted: 30 July 1996     

Hydrochemical appraisal of groundwater and its suitability in the intensive agricultural area of Muzaffarnagar district,Uttar Pradesh,India

Muzaffarnagar is an economically rich district situated in the most fertile plains of two great rivers Ganga and Yamuna in the Indo-gangetic plains, with agricultural land irrigated by both surface water as well as groundwater. An investigation has been carried out to understand the hydrochemistry of the groundwater and its suitability for irrigation uses. Groundwater in the study area is neutral to moderately alkaline in nature. Chemistry of groundwater suggests that alkaline earths (Ca + Mg) significantly exceed the alkalis (Na + K) and weak acids exceed the strong acids (Cl + SO₄), suggesting the dominance of carbonate weathering followed by silicate weathering. Majority of the groundwater samples (62%) posses Ca–Mg–HCO₃ type of hydrochemical species, followed by Ca–Na–Mg–HCO₃, Na–Ca–Mg–HCO₃, Ca–Mg–Na–HCO₃–Cl and Na–Ca–HCO₃–SO₄ types. A positive high correlation (r ² = 0.928) between Na and Cl suggests that the salinity of groundwater is due to intermixing of two or more groundwater bodies with different hydrochemical compositions. Barring a few locations, most of the groundwater samples are suitable for irrigation uses. Chemical fertilizers, sugar factories and anthropogenic activities are contributing to the sulphate and chloride concentrations in the groundwater of the study area. Overexploitation of aquifers induced multi componential mixing of groundwater with agricultural return flow waters is responsible for generating groundwater of various compositions in its lateral extent.     

Evaluation of hydrogeochemical processes in arsenic-contaminated alluvial aquifers in parts of Mid-Ganga Basin,Bihar, Eastern India

The study region covers 1,650 km² of the Mid-Ganga Basin in Bihar, experiencing intensive groundwater draft. The area forms a part of the Gangetic alluvial plain where high incidence of arsenic groundwater contamination (>50 μg/l) has recently been detected. Seventy-seven groundwater samples have been collected and analysed for major ions, iron and arsenic. Arsenic contamination (max 620 μg/l) is confined in hand pump zones (15–35 m) within the newer alluvium deposited during Middle Holocene to Recent age. The older alluvial aquifers are arsenic-safe and recorded maximum concentration as 9 μg/l. Out of 12 hydrochemical facies identified, four have been found arsenic-affected: Ca–HCO₃, Mg–HCO₃, Ca–Mg–HCO₃ and Mg–Ca–HCO₃. The geochemical evolution of groundwater, as investigated by graphical interpretation and statistical techniques (correlation, principal component analysis) revealed that dissolution of detrital calcite, dolomite and infiltration of rainwater are the major processes shaping the groundwater chemistry in the newer alluvium. Arsenic and iron showed strong positive correlation. Rainfall infiltration, carrying organic matter from recently accumulated biomass from this flood-prone belt, plays a critical role in releasing arsenic and iron present in the sediments. Geochemical evolution of groundwater in older alluvium follows a different path, where cation-exchange has been identified as a significant process.     

Groundwater hydrochemistry of a sugarcane cultivation belt in parts of Muzaffarnagar district, Uttar Pradesh, India

The Kali-Hindon is a watershed in the most productive central Ganga plain of India. The whole area is a fertile track with sugarcane being the principal crop. Systematic sampling was carried out to assess the source of dissolved ions, impact of sugar factories and the quality of groundwater. Thirty-six samples were collected covering an area of 395 km². The quality of groundwater is suitable for irrigational purposes but is rich in SO₄ which is not best for human consumption. Graphical treatment of major ion chemistry helps identify six chemical types of groundwater. All possible species such as Na–Cl, K–Cl, Na–HCO₃, Na–SO₄, Ca–HCO₃, Mg–HCO₃, Ca–SO₄ and Mg–SO₄ are likely to occur in the groundwater system. The most conspicuous change in chemistry of groundwater is relative enrichment of SO₄. The interpretation of data reveals that SO₄ has not been acquired through water–rock interaction. The source of SO₄ is anthropogenic. Sugar factories alone are responsible for this potential environmental hazard.     

Groundwater geochemical evolution in the northern portion of the Guarani Aquifer System (Brazil) and its relationship to diagenetic features

The groundwater flow pattern in the northern portion of GAS (Guarani Aquifer System) is characterized by the existence of four regional recharge areas located in São Paulo, Mato Grosso do Sul and Goiás states. From these areas of recharge the regional flow is radial and directed toward the center of the Paraná Sedimentary Basin. Local discharge occurs in portions of outcrop regions. The groundwater has low mineralization and can be classified as Ca or Ca–Mg–HCO₃ type, Na–HCO₃ type and Na–HCO₃/Cl/SO₄ type, this sequence represents the hydrochemical evolution. The mechanisms responsible for this evolution are dissolution of feldspars and removal of the carbonate cement from the sandstone mineral framework, followed by ion exchange, responsible for the increase in the Na concentration and decrease of Ca, and, finally, enrichment in Cl and SO₄ derived from underlying aquifer units. The hydrochemical evolution is consistent with diagenetic features that are observed in the sandstones, with the presence of siliceous cement in the outcrop areas, and carbonate cement toward the center of Paraná Basin.     

Chemical characteristics of groundwater in parts of mountainous region, Alvand, Hamadan, Iran

Eighty-seven groundwater samples have been collected from a mountainous region (Alvand, Iran) for hydrochemical investigations to understand the sources of dissolved ions and assess the chemical quality of the groundwater. Most water quality parameters are within World Health Organization acceptable limits set for drinking water. The least mineralized water is found closest to the main recharge zones and the salinity of water increased towards the north of the basin. The most prevalent water type is Ca–HCO₃ followed by water types Ca–NO₃, Ca–Cl, Ca–SO₄ and Mg–HCO₃. The Ca–NO₃ water type is associated with high nitrate pollution. Agricultural and industrial activities were associated with elevated level of NO₃⁻. Mineral dissolution/weathering of evaporites dominates the major element hydrochemistry of the area. Chemical properties of groundwater in Alvand region are controlled both by natural geochemical processes and anthropogenic activities.     

A topo-geochemical sequence study of groundwater in Asa drainage basin, Kwara State, Nigeria

 A strong geochemical gradient was observed in the thick overburden aquifer of the Asa drainage basin. Different types of groundwater occur at different (downslope) locations and groundwater table depths. The following sequence was noticed with increasing distance downslope or with increasing groundwater table depth: 1. Ca–Mg–HCO₃ water at about 390-m groundwater table elevations or upslope locations. 2. Ca–Mg–HCO₃–Cl water at middle-slope locations or groundwater table elevations of about 350 m above sea level; 3. Ca–Mg–SO₄–Cl water at downslope locations or groundwater table elevations of about 300 m above sea level. In this basin, changes in the type of water are expected at about every 40–50 m depth from the surface. Statistical analysis via the determination of the correlation coefficient (r) and regression analysis shows that about 80–99% of the variation in groundwater chemistry is accounted for by the topography, using the model presented in this paper. The rate of change in the sequence will depend on the permeability of the aquifer, which determines the rate of groundwater flow and the residence time, and the nature of recharge. Received: 4 February 1997 · Accepted: 22 July 1997     

Is groundwater in the Tarkwa gold mining district of Ghana potable?

Hand-pump wells in the Tarkwa gold mining district and the geologically similar Bui area were chemically analysed and compared in an effort to determine whether groundwaters in the Tarkwa area have been affected by mining. Significant chemical differences attributed to mine water discharges have been observed in streams in the Tarkwa area. Groundwater chemistry from hand-pump wells in Tarkwa and Bui areas reveal similar hydrochemical facies, predominantly Ca–Na–Mg–HCO₃–Cl. However, except for SO₄^2–, ionic concentrations of groundwaters from Bui are greater than those from Tarkwa probably due to differences in (1) water availability during sedimentation (2) water-rock interactions and/or residence times for water. No demonstrable impact of mining on groundwaters from hand-pumped wells in the Tarkwa area has been noted. Hydrogeological inference suggests that the main streams which receive mine water discharges are both gaining and are groundwater divides. The overwhelming majority of population centres and mining operations are located on opposite sides of these groundwater divides, therefore, it is unlikely aquifers tapped for drinking by these communities would be affected by mining.     

Hydrochemical baseline condition of groundwater at the Mizunami underground research laboratory (MIU)

Hydrochemical conditions up to depths of 1000 m below ground level around the Mizunami Underground Research Laboratory were investigated to construct a “baseline condition model” describing the undisturbed hydrochemical environment prior to excavation of the underground facilities at Mizunami, Gifu, Japan. Groundwater chemistry in this area was classified into a Na–Ca–HCO₃ type of groundwater in the upper part of sedimentary rock sequence and a Na–(Ca)–Cl type of groundwater in the deeper part of the sedimentary rock sequence and basement granite. The residence time of the groundwaters was estimated from their ¹⁴C contents to be approximately 9.3 ka in the middle part of the sedimentary rock and older than 50 ka in the deep part of the granite. The evolution processes of these groundwaters were inferred to be water–rock interactions such as weathering of plagioclase, dissolution of marine sulphate/sulphide minerals and carbonate minerals in the Na–Ca–HCO₃ type of groundwater, and mixing between “low-salinity water” in the shallow part and “higher-salinity water” in the deeper part of the granite in the Na–(Ca)–Cl type of groundwater. The source of salinity in the deeper part of the granite was possibly a palaeo-hydrothermal water or a fossil seawater that recharged in the Miocene, subsequently being modified by long-term water–rock interaction. The Cl-depth trend in granitic groundwater changes at a depth of −400 m below sea level. The hydrogeological properties controlling the groundwater flow and/or mixing processes such as advection and diffusion were inferred to be different at this depth in the granite. This hydrochemical conceptual model is indispensable not only when constructing the numerical model for evaluating the hydrochemical disturbance during construction and operation of the MIU facility, but also when confirming a hydrogeological model.     

Groundwater quality and its suitability for drinking and agricultural use in Chithar River Basin, Tamil Nadu, India

Hydrochemistry of groundwater in Chithar Basin, Tamil Nadu, India was used to assess the quality of groundwater for determining its suitability for drinking and agricultural purposes. Physical and chemical parameters of groundwater such as electrical conductivity, pH, total dissolved solids (TDS), Na⁺, K⁺, Ca²⁺, Mg²⁺, Cl^–, HCO₃^–, CO₃^2–, SO₄^2–, NO^–₃, F^–, B^– and SiO₂ were determined. Concentrations of the chemical constituents in groundwater vary spatially and temporarily. Interpretation of analytical data shows that mixed Ca–Mg–Cl, Ca–Cl and Na–Cl are the dominant hydrochemical facies in the study area. Alkali earths (Ca²⁺, Mg²⁺) and strong acids (Cl^–, SO₄^2–) are slightly dominating over alkalis (Na⁺, K⁺) and weak acids (HCO₃^–, CO₃^2–). The abundance of the major ions is as follows: Na⁺ Ca²⁺ Mg²⁺ > K⁺ = Cl^– > HCO₃^–> SO₄^2– > NO₃^– > CO₃^2– . Groundwater in the area is generally hard, fresh to brackish, high to very high saline and low alkaline in nature. High total hardness and TDS in a few places identify the unsuitability of groundwater for drinking and irrigation. Such areas require special care to provide adequate drainage and introduce alternative salt tolerance cropping. Fluoride and boron are within the permissible limits for human consumption and crops as per the international standards.     

Hydrogeochemistry of groundwater and anthropogenic control over dolomitization reactions in alluvial sediments of the Deoria district: Ganga plain,India

Groundwater is a critical resource in Deoria district, as it is the main source of drinking water and irrigation. The aquifer has deteriorated to a high degree, during the last two to three decades, in quality and quantity due to high population growth and environmental pollution. More than 90% of the population get their drinking water from subsurface waters. Fifteen wells were sampled in June 2006 to probe the hydrogeochemical components that influence the water quality. The results show that groundwater have EC, TDS, Na⁺, Mg²⁺, HCO₃⁻ and TH higher than the WHO, 1997 maximum desirable limits. A hydrogeochemical numerical model for carbonate minerals was constructed using the PHREEQC package. The regression analysis shows that there are three groups of elements which are significantly and positively correlated. The main hydrochemical facies of the aquifer (Ca + Mg–HCO₃) represents 33.33% of the total wells. The geochemical modeling demonstrated that the reactions responsible for the hydrochemical evolution in the area fall into three categories: (1) dissolution of salts, (2) precipitation of dolomite, (3) ion exchange. Solubility of dolomite, calcite, aragonite and gypsum were assessed in terms of the saturation index. The thermodynamic prerequisites for dolomite supersaturation reactions are satisfied by subsurface waters, since they are supersaturated with respect to dolomite, undersaturated (or in equilibrium) with respect to calcite, and undersaturated with respect to gypsum. The Ca²⁺ versus SO₄²⁻ and Mg²⁺ versus SO₄²⁻ trends are also compatible with homologous trends resulting from dolomite supersaturation.     

Groundwater contamination with arsenic in Sherajdikhan,Bangladesh: geochemical and hydrological implications

An integrated study has been carried out to elucidate the distribution and occurrence of arsenic in selected groundwater samples in the area of Sherajdikhan, Bangladesh. Arsenic and other parameters (T, pH, EC, Na⁺, K⁺, Ca²⁺, Mg²⁺, Cl⁻, NO₃ ⁻, SO₄ ²⁻, HCO₃ ⁻, PO₄ ³⁻, Fe, Mn and DOC) have been measured in groundwater samples collected from shallow/deep tube wells at different depths. Hydrogeochemical data suggest that the groundwaters are generally Ca–Mg–HCO₃ and Mg–Ca–HCO₃ types with bicarbonate (HCO₃ ⁻) as the dominant anion, though the other type of water has also been observed. Dissolved arsenic in groundwater ranged from 0.006 to 0.461 mg/l, with 69% groundwater samples exceeded the Bangladesh limit for safe drinking water (0.05 mg/l). Correlation and principal component analysis have been performed to find out possible relationships among the examined parameters in groundwater. Low concentrations of NO₃ ⁻ and SO₄ ²⁻, and high concentrations of DOC, HCO₃ ⁻ and PO₄ ³⁻ indicate the reducing condition of subsurface aquifer where sediments are deposited with abundant organic matter. Distinct relationship of As with Fe and Mn, and strong correlation with DOC suggests that the biodegradation of organic matter along with reductive dissolution of Fe–Mn oxyhydroxides has being considered the dominant process to release As in the aquifers studied herein.     

Hydro-environmental status and soil management of the River Nile Delta,Egypt

The sea level rise has its own-bearing on the coastal recession and hydro-environmental degradation of the River Nile Delta. Attempts are made here to use remote sensing to detect the coastal recession in some selected parts and delineating the chemistry of groundwater aquifers and surface water, which lie along south-mid-northern and coastal zone of the Nile Delta. Eight water samples from groundwater monitoring wells and 13 water samples from surface water were collected and analyzed for various hydrochemical parameters. The groundwater samples are classified into five hydrochemical facies on Hill-Piper trilinear diagram based on the dominance of different cations and anions: facies 1: Ca–Mg–Na–HCO₃–Cl–SO₄ type I; facies 2: Na–Cl–HCO₃ type II; facies 3: Na–Ca–Mg–Cl type III, facies 4: Ca–Na–Mg–Cl–HCO₃ type IV and facies 5: Na–Mg–Cl type V. The hydrochemical facies showed that the majority of samples were enriched in sodium, bicarbonate and chloride types and, which reflected that the sea water and tidal channel play a major role in controlling the groundwater chemical composition in the Quaternary shallow aquifers, with a severe degradation going north of Nile Delta. Also, the relationship between the dissolved chloride (Cl, mmol/l), as a variable, and other major ion combinations (in mmol/l) were considered as another criterion for chemical classification system. The low and medium chloride groundwater occurs in southern and mid Nile Delta (Classes A and B), whereas the high and very high chloride (classes D and C) almost covers the northern parts of the Nile Delta indicating the severe effect of sea water intrusion. Other facets of hydro-environmental degradation are reflected through monitoring the soil degradation process within the last two decades in the northern part of Nile Delta. Land degradation was assessed by adopting new approach through the integration of GLASOD/FAO approach and Remote Sensing/GIS techniques. The main types of human induced soil degradation observed in the studied area are salinity, alkalinity (sodicity), compaction and water logging. On the other hand, water erosion because of sea rise is assessed. Multi-dates satellite data from Landsat TM and ETM+ images dated 1983 and 2003 were used to detect the changes of shoreline during the last two decades. The obtained results showed that, the eroded areas were determined as 568.20 acre; meanwhile the accreted areas were detected as 494.61 acre during the 20-year period.     

Groundwater hydrochemistry and origin in the south-eastern part of Wadi El Natrun,Egypt

The demand for water is rapidly increasing in Egypt, because of high population and agriculture production growth rate, which makes research of water resources necessary. The regional multi-aquifer system of the Miocene–Pleistocene age is discharged in Wadi El Natrun area. Intensive aquifer overexploitation and agricultural development in the area are related to groundwater quality deterioration. Hydrochemical and hydrogeological data was evaluated to determine the groundwater origin and quality in the south-eastern part of wadi, which appears to be more significant for water supply owing to lower groundwater salinity. The dominance of the high mineralised Cl groundwater type was found; however, also less mineralised SO₄ and HCO₃ types were identified there. Based on the ion relations, halite and gypsum dissolution and ion exchange are the most important hydrochemical processes forming the groundwater chemical composition. The Cl dominated groundwater matches the discharge part of the regional hydrogeological system. Contrary, the presence of HCO₃ and SO₄ hydrochemical types corresponds to the infiltration and transferring parts of the hydrogeological system indicating the presence of zones conducting low mineralised groundwater. The discharge area of the over-pumped aquifer in Wadi El-Natrun lies 23 m beneath the sea level with the shoreline being at the distance of 100 km, thus there is a real risk of seawater intrusion. Using the hydrochemical facies evolution diagram, four samples in the centre of the discharge area indicate advanced seawater intrusion. The zones of the highest demand for groundwater quality protection were indicated based on a spatial pattern of hydrogeochemical composition.     

Influence of hydrogeochemical processes on temporal changes in groundwater quality in a part of Nalgonda district, Andhra Pradesh, India

Geochemical processes that take place in the aquifer have played a major role in spatial and temporal variations of groundwater quality. This study was carried out with an objective of identifying the hydrogeochemical processes that controls the groundwater quality in a weathered hard rock aquifer in a part of Nalgonda district, Andhra Pradesh, India. Groundwater samples were collected from 45 wells once every 2 months from March 2008 to September 2009. Chemical parameters of groundwater such as groundwater level, EC and pH were measured insitu. The major ion concentrations such as Ca²⁺, Mg²⁺, Na⁺, K⁺, Cl⁻, and SO₄ ²⁻ were analyzed using ion chromatograph. CO₃ ⁻ and HCO₃ ⁻ concentration was determined by acid–base titration. The abundance of major cation concentration in groundwater is as Na⁺ > Ca²⁺ > Mg²⁺ > K⁺ while that of anions is HCO₃ ⁻ > SO₄ ²⁻ > Cl⁻ > CO₃ ⁻. Ca–HCO₃, Na–Cl, Ca–Na–HCO₃ and Ca–Mg–Cl are the dominant groundwater types in this area. Relation between temporal variation in groundwater level and saturation index of minerals reveals the evaporation process. The ion-exchange process controls the concentration of ions such as calcium, magnesium and sodium. The ionic ratio of Ca/Mg explains the contribution of calcite and dolomite to groundwater. In general, the geochemical processes and temporal variation of groundwater in this area are influenced by evaporation processes, ion exchange and dissolution of minerals.     

Integrated hydrochemical method of water quality assessment for irrigation in arid areas: application to the Jilh aquifer, Saudi Arabia

Water samples from 72 wells tapping the Jilh aquifer were collected and analyzed for 10 different water quality parameters. Using these data, a regional irrigation water quality was assessed using three techniques: (i) United States Department of Agriculture method (USDA), (ii) Food and Agriculture Organization (FAO) guidelines for water quality assessment, and (iii) Water-Types approach. The USDA method revealed that the aquifer water salinity, as represented by electrical conductivity, EC_w, ranges from high salinity (C3: EC_w > 0.75–2.25 dS/m) to a very high salinity (C4: EC_w > 2.25 dS/m). The sodium adsorption ratio (SAR) varied from low (S1) to very high (S4) sodicity. Therefore, the water of the Jilh aquifer is dominantly of the C4–S2 class representing 56% of the total wells followed by C4–S1, C4–S3, C3–S1 and C4–S4 classes at 19%, 14%, 8%, and 3% of the wells respectively. The FAO system indicated moderate to severe restriction on the use for irrigation and slight to moderate ion toxicities for Na⁺, Cl⁻, B⁺, NO₃⁻ and HCO₃⁻. It is clear that, both USDA and FAO systems condemn the Jilh groundwater as hazardous for irrigation due to its high salt content, unless certain measures for salinity control are undertaken. The dominant salt constituents in the water are Mg–Cl₂, Na–Cl and Ca–Cl₂ as per the Water-Types method. However, due to the complexity in classifying the aquifer groundwater for irrigation, a simplified approach acknowledging three class groups (I-suitable water, II-conditionally suitable water and III-unsuitable water) adopted from the three methods, is suggested in this paper. The simplified approach combines C–S classes of the USDA method among these three groups according to the lowest ratings. The salinity of the FAO method has been split arbitrarily into slight and moderate subclasses with values of 0.7–2.25 and >2.25 dS/m, respectively; to match with the C3-class of the USDA system. The Water-Types were classified assuming that Ca–Cl₂ is the least hazardous salt, followed by Mg–Cl₂ and Na–Cl. Using this integrated hydrochemical method, the majority of the wells (92%) contain unsuitable water for irrigation (Group III) while the remaining wells (8%) are in Group II with water considered conditionally suitable for irrigation.     

Assessment of natural and anthropogenic influences on regional groundwater chemistry in a highly industrialized and urbanized region: a case study of the Vaal River Basin,South Africa

The Vaal River Basin is an economically significant area situated in the interior of South Africa (SA), where mining, industrial, domestic and agricultural activities are very intense. The purpose of the study was to assess the influence of geology and anthropogenic activities on groundwater chemistry, and identify the predominant hydrochemical processes in the basin. Data from seventy groundwater sites were retrieved from the national database, and attention was paid to fifteen water quality parameters. Groundwater samples were clustered into seven hydrochemically distinct groups using Hierarchical Cluster Analysis (HCA), and three samples treated independently. A Piper plot revealed two major water types, Ca–Mg–HCO₃ and Ca–Mg–SO₄-Cl, which were linked to dissolution of the underlying geology and mine pollution. The Ca?+?Mg vs HCO₃?+?SO₄ plot indicated that reverse ion exchange is an active process than cation exchange in the area. Principal component analysis (PCA) was used to identify the main natural and anthropogenic processes causing variation in groundwater chemistry. Four principal components were extracted using PCA that explains 82% of the total variance in the chemical parameters. The PCA results can be categorized by four components: (1) evaporites and silicates weathering enrichment of Na, K, Cl, SO₄ and F, and anthropogenic Cl; (2) dissolution of dolomite, limestone and gypsum; (3) agricultural fertilizers (4) wastewater treatment. This study reveals that both natural and anthropogenic activities are the cause of groundwater variation in the basin.     

Hydrogeological and mixing process of waters in aquifers in arid regions: a case study in San Luis Potosi Valley,Mexico

The climatic conditions of arid regions are characterized by high temperatures, low precipitation and high evapotranspiration rates that can explain the reduced recharge of aquifers. Thus, in these regions, there are some problems related to the groundwater quality and recharge that makes worse the problem of groundwater supply. A model, taking into account ternary mixtures, is presented and applied to a case study: the aquifer of San Luis Potosi valley located in the highlands of the central part of Mexico. In this valley, four hydrochemical facies were identified that correspond to the Ca–Na + K–HCO₃, Na + K–Ca–HCO₃, Ca–HCO₃ and Ca–SO₄ types. From this characterization, it was found out that the recharge area (known as Bledos Graben) is located at the SE of the valley; the deep water flow comes from there (Villa de Reyes and Alvarez Range) to the center of the valley. Mixture fractions were obtained by using chlorides and fluorides as conservative elements, from which it was possible to quantify the contribution of each member to the groundwater quality. According to these results, the contributions to the water extracted from this aquifer are as follows: shallow flows 50%, deep flows from Villa de Reyes 27%, and flows coming from the Alvarez Ranges about 15%.     

Effect of mining on geochemistry of groundwater in Permo-carboniferous Gondwana coalfields: Raniganj Basin, India

Lack of proper reclamation strategy and indiscriminate mining of various economic resources, particularly coal from Permo-carboniferous Gondwana coalfields affects the groundwater quality of the concerned regions. Leaching from mine-tailings along with seasonal fluctuation of water table caused a significant change in groundwater geochemistry of Raniganj coalfield area. Gondwana sequences, developed in intracratonic rift basin, are characterized by numerous longitudinal and cross faults. This results in the formation of many small aquifer systems which may be interconnected laterally as well as vertically providing the conduit for homogenization of aquifers. Although the predominance of major cations (Ca>Na>Mg>K) and anions (HCO₃>Cl>SO₄>NO₃) remain same irrespective of season, the dominance of Na and SO₄ have significantly increased in post-monsoon season. The types of groundwater in pre-monsoon and postmonsoon seasons are CaMgCl and CaHCO₃ respectively. Leaching of SO₄ from surface sources (mine tailings) has increased TDS in post-monsoon. Base exchange (direct and reverse) reactions have taken place between aquifer materials and groundwater.     

Study of hydrogeochemical processes of the groundwater in Ghatprabha river sub-basin, Bagalkot District, Karnataka, India

The alluvial aquifer of the Ghatprabha River comprises shallow tertiary sediment deposits underlain by peninsular gneissic complex of Archean age, located in the central–eastern part of the Karnataka in southern India. In order to establish the baseline hydrochemical conditions and processes determining the groundwater quality, groundwater samples were collected as part of an integrated investigation that coupled multivariate statistical analysis with hydrochemical methods to identify and interpret the groundwater chemistry of the aquifer system. Three main hydrochemical types (Ca–Mg–Cl, Ca–Mg–HCO₃, and Na–SO₄) were identified. Gibbs plots indicate that the evolution of water chemistry is influenced by water–rock interaction followed by evapotranspiration process. The results of factor analysis indicated the total variance explained by the extracted factor 79.9% and 87.1% for both pre- and post-monsoon, respectively. And other processes such as silicate weathering, ion exchange, and local anthropogenic activities affect the groundwater chemistry.