Identification of major sources controlling groundwater chemistry from a hard rock terrain — A case study from Mettur taluk,Salem district,Tamil Nadu,India

The study area Mettur forms an important industrial town situated NW of Salem district. The geology of the area is mainly composed of Archean crystalline metamorphic complexes. To identify the major process activated for controlling the groundwater chemistry an attempt has been made by collecting a total of 46 groundwater samples for two different seasons, viz., pre-monsoon and post-monsoon. The groundwater chemistry is dominated by silicate weathering and (Na + Mg) and (Cl + SO₄) accounts of about 90% of cations and anions. The contribution of (Ca + Mg) and (Na + K) to total cations and HCO₃ indicates the domination of silicate weathering as major sources for cations. The plot for Na to Cl indicates higher Cl in both seasons, derived from Anthropogenic (human) sources from fertilizer, road salt, human and animal waste, and industrial applications, minor representations of Na also indicates source from weathering of silicate-bearing minerals. The plot for Na/Cl to EC indicates Na released from silicate weathering process which is also supported by higher HCO₃ values in both the seasons. Ion exchange process is also activated in the study area which is indicated by shifting to right in plot for Ca + Mg to SO₄ + HCO₃. The plot of Na-Cl to Ca + Mg-HCO₃-SO₄ confirms that Ca, Mg and Na concentrations in groundwater are derived from aquifer materials. Thermodynamic plot indicates that groundwater is in equilibrium with kaolinite, muscovite and chlorite minerals. Saturation index of silicate and carbonate minerals indicate oversaturation during pre-monsoon and undersaturation during post-monsoon, conforming dissolution and dilution process. In general, water chemistry is guided by complex weathering process, ion exchange along with influence of Cl ions from anthropogenic impact.     

Environmental geochemistry of Damodar River basin, east coast of India

 Water and bed sediment samples collected from the Damodar River and its tributaries were analysed to study elemental chemistry and suspended load characteristics of the river basin. Na and Ca are the dominant cations and HCO₃ is the dominant anion. The water chemistry of the Damodar River basin strongly reflects the dominance of continental weathering aided by atmospheric and anthropogenic activities in the catchment area. High concentrations of SO₄ and PO₄ at some sites indicate the mining and anthropogenic impact on water quality. The high concentration of dissolved silica, relatively high (Na+K)/TZ⁺ ratio (0.2–0.4) and low equivalent ratio of (Ca+Mg)/(Na+K) indicate that dissolved ions contribute significantly to the weathering of aluminosilicate minerals of crystalline rocks. The seasonal data show a minimum ionic concentration in the monsoon season, reflecting the influence of atmospheric precipitation on total dissolved solids contents. The suspended sediments show a positive correlation with discharge and both discharge and suspended load reach their maximum value during the monsoon season. Kaolinite is the mineral that is possibly in equilibrium with the water. This implies that the chemistry of the Damodar River water favours kaolinite formation. The concentration of heavy metals in the finer size fraction (<37 μ m) is significantly higher than the bulk composition. The geoaccumulation index values calculated for Fe, Mn, Zn, Ni and Cr are well below zero, suggesting that there is no pollution from these metals in Damodar River sediments. Received: 21 January 1998 · Accepted: 4 May 1998     

Major ion chemistry,weathering processes and water quality assessment in upper catchment of Damodar River basin,India

The chemical characteristics of surface, groundwater and mine water of the upper catchment of the Damodar River basin were studied to evaluate the major ion chemistry, geochemical processes controlling water composition and suitability of water for domestic, industrial and irrigation uses. Water samples from ponds, lakes, rivers, reservoirs and groundwater were collected and analysed for pH, EC, TDS, F, Cl, HCO₃, SO₄, NO_3, Ca, Mg, Na and K. In general, Ca, Na, Mg, HCO₃ and Cl dominate, except in samples from mining areas which have higher concentration of SO₄. Water chemistry of the area reflects continental weathering, aided by mining and other anthropogenic impacts. Limiting groundwater use for domestic purposes are contents of TDS, F, Cl, SO₄, NO₃ and TH that exceed the desirable limits in water collected from mining and urban areas. The calculated values of SAR, RSC and %Na indicate good to permissible use of water for irrigation. High salinity, %Na, Mg-hazard and RSC values at some sites limit use for agricultural purposes.     

Assessment of groundwater quality with special emphasis on fluoride contamination in crystalline bed rock aquifers of Mettur region, Tamilnadu, India

Groundwater samples were collected from Mettur taluk of Salem district, Tamilnadu, India for two different seasons (pre-monsoon and post-monsoon) and analyzed for fluoride ion along with other chemical parameters. The major litho units of the study area are Charnockites, peninsular gneiss, and calc gneiss of meta-sedimentary group. The fluoride concentration ranges from 0.1 to 2.8?mg/L and 0.4 to 4.0?mg/L during pre-monsoon (PRM) and post-monsoon (POM) seasons, respectively. Results showed that collected water samples were contaminated by the presence of fluoride ion. During PRM and POM, 21% and 56% of samples recorded higher fluoride when compared with Indian Drinking Water Standard (1?mg/L) and (9% and 35%) of samples recorded higher fluoride when compared with World Health Organization tolerance limit (1.5?mg/L). The ratio of Na/Ca indicates high sodium content in groundwater enhances the dissolution of fluoride at higher pH. Hydrogeochemical facies indicates water-rock interaction as main source for high fluoride in groundwater. A positive correlation between pH, Mg, and F indicates high alkaline nature of water promotes fluoride leaching from source rocks into ground water. Factor analysis indicates hydro-geochemical processes like weathering, ion exchange, and anthropogenic contributes to groundwater chemistry. The saturation index indicates dissolution and precipitation contributes fluoride dissolution along with mixing.     

Geochemical Eccentricity of Ground Water Allied to Weathering of Basalts from the Deccan Volcanic Province,India: Insinuation on CO<Subscript>2</Subscript> Consumption

Analyses of 72 samples from Upper Panjhara basin in the northern part of Deccan Plateau, India, indicate that geochemical incongruity of groundwater is largely a function of mineral composition of the basaltic lithology. Higher proportion of alkaline earth elements to total cations and HCO₃>Cl + SO₄ reflect weathering of primary silicates as chief source of ions. Inputs of Cl, SO₄, and NO₃ are related to rainfall and localized anthropogenic factors. Groundwater from recharge area representing Ca + Mg–HCO₃ type progressively evolves to Ca + Na–HCO₃ and Na–Ca–HCO₃ class along flow direction replicates the role of cation exchange and precipitation processes. While the post-monsoon chemistry is controlled by silicate mineral dissolution + cation exchange reactions, pre-monsoon variability is attributable chiefly to precipitation reactions + anthropogenic factors. Positive correlations between Mg vs HCO₃ and Ca + Mg vs HCO₃ supports selective dissolution of olivine and pyroxene as dominant process in post-monsoon followed by dissolution of plagioclase feldspar and secondary carbonates. The pre-monsoon data however, points toward the dissolution of plagioclase and precipitation of CaCO₃ supported by improved correlation coefficients between Na + Ca vs HCO₃ and negative correlation of Ca vs HCO₃, respectively. It is proposed that the eccentricity in the composition of groundwater from the Panjhara basin is a function of selective dissolution of olivine > pyroxene followed by plagioclase feldspar. The data suggest siallitization (L < R and R _k) as dominant mechanism of chemical weathering of basalts, stimulating monosiallitic (kaolinite) and bisiallitic (montmorillonite) products. The chemical denudation rates for Panjhara basin worked out separately for the ground and surface water component range from 6.98 to 36.65 tons/km²/yr, respectively. The values of the CO₂ consumption rates range between 0.18 × 10⁶ mol//km²/yr (groundwater) and 0.9 × 10⁶ mol/km²/yr (surface water), which indicates that the groundwater forms a considerable fraction of CO₂ consumption, an inference, that is, not taken into contemplation in most of the studies.     

Hydrochemistry and quality assessment of groundwater in part of NOIDA metropolitan city,Uttar Pradesh

An attempt has been made to study the groundwater geochemistry in part of the NOIDA metropolitan city and assessing the hydrogeochemical processes controlling the water composition and its suitability for drinking and irrigation uses. The analytical results show that Na and Ca are the major cations and HCO₃ and Cl are the major anions in this water. The higher ratios of Na+K/TZ⁺ (0.2–0.7), Ca+Mg/HCO₃ (0.8–6.1); good correlation between Ca-Mg (0.75), Ca-Na (0.77), Mg-Na (0.96); low ratio of Ca+Mg/Na+K (1.6), Ca/Na (1.03), Mg/Na (0.64), HCO₃/Na (1.05) along with negative correlation of HCO₃ with Ca and Mg signify silicate weathering with limited contribution from carbonate dissolution. The hydro-geochemical study of the area reveals that many parameters are exceeding the desirable limits and quality of the potable water has deteriorated to a large extent at many sites. High concentrations of TDS, Na, Cl, SO₄, Fe, Mn, Pb and Ni indicate anthropogenic impact on groundwater quality and demand regional water quality investigation and integrated water management strategy. SAR, %Na, PI and Mg-hazard values show that water is of good to permissible quality and can be used for irrigation. However, higher salinity and boron concentration restrict its suitability for irrigation uses at many sites.     

A Statistical appraisal to hydrogeochemistry of fluoride contaminated ground water in Nayagarh district, Odisha

Seasonal variation of ground water in Nayagarh district, Odisha is determined by analysing both pre and post monsoon water samples. The high fluoride content is an endemic problem in the area and special attention was attached to the point. The chemical compositions of the ground water of the area are dominated by CaCl, NaCl and mixed CaMgCl types in pre-monsoon and CaHCO₃-mixed CaMgCl type in post-monsoon. This is largely due to chemical weathering of Eastern Ghats Mobile Belt rock types. Increasing alkalinity vis-a-vis F concentration in pre-monsoon is associated with sodium-bicarbonate water types having high pH (>7) and low calcium and magnesium contents. The percentage of total high fluoride containing water samples is nearly double in pre-monsoon than in post-monsoon. During both the seasons, pH values indicate mildly alkaline to weakly acidic nature of the water samples. Fluoride concentration has good correlation with pH in pre-monsoon whereas in post-monsoon it shows good correlation with Fe. Facies analysis indicates that water is becoming predominantly Ca-Na cation and Cl-SO₄-HCO₃ anion type in premonsoon than Ca-Mg type and HCO₃-Cl-SO₄ type in post-monsoon. The seasonal variations in concentrations of anthropogenic components demonstrate that the groundwater system is very less liable to pollution by human activities.     

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.     

Geochemical characteristics of water and sediment from the Dal Lake, Kashmir Himalaya: constraints on weathering and anthropogenic activity

Two hundred and forty water samples (in four seasons) and seventeen sediment samples have been analyzed to monitor the natural and anthropogenic influences on the water and sediment chemistry of the Dal Lake, Kashmir Himalaya. The scatter diagrams [(Ca+Mg)/total cations (TZ⁺), (Ca+Mg)/HCO₃, (Ca+Mg)/(HCO₃₊SO₄), (Na+K)/TZ⁺; (Ca+Mg)/(Na+K)] and the geological map of the study area suggest predominance of carbonate and silicate weathering. Lower pH and high total dissolved solids, electrical conductivity and values in the Gagribal basin and in some patches of other basins reflect anthropogenic inputs in the form of sewage from surrounding population, houseboats, hotels, etc. The Dal Lake is characterized by high chemical index of alteration (CIA: 87–95), reflecting extreme weathering of the catchment area. Relative to the average carbonates, the lakebed sediments are enriched in Al, Ti, Zn, Cu and Co and depleted in Ni and Mn. Compared to the post-Archean Shale the sediments have higher Al, Zn and Cu contents and lower Ni and Co. There are distinct positive anomalies of Al, Mn, Zn and Cu and negative anomalies of Ni and Pb with respect to the upper continental crust. Geoaccumulation index (I _geo) and the US Environmental Protection Agency sediment quality standards indicate that the Gagribal basin and some patches of the Nagin basin are polluted with respect to Zn, Cu and Pb. These data suggest that the Dal Lake is characterized by differential natural and anthropogenic influences.     

Development of Water Quality Index (WQI) model for the groundwater in Tirupur district, South India

Groundwater quality of the Tiruppur district in Tamil Nadu was investigated in this study to develop a Water Quality Index (WQI) model. Hydrochemical parameters showed tremendous variation in certain location over the seasons. Ionic chemistry of groundwater suggested that textile industries and rock-water interaction are major threats to the water quality. Analysis of Na and Ca concentration indicates that direct as well as the inverse cation exchange controls the natural cation chemistry. NO3 concentration shows that the pre-monsoon samples were affected by the fertilizer usage in agricultural fields. Na-Cl type of the water was dominant throughout the study area except few locations. WQI showed that 55% of the pre-monsoon samples and the 47% of the post monsoon samples were classified as poor/very poor/unsuitable for drinking category. Leaching of the textile waste and their transport to the downstream was well observed during the post-monsoon season. The specific contribution of river Noyyal in the transport of the solutes to the discharge zones was proved by the hydrochemistry of the samples.     

Major ion chemistry and metal distribution in coal mine pit lake contaminated with industrial effluents: constraints of weathering and anthropogenic inputs

Ion chemistry of mine pit lake water reveals dominance of alkaline earths (Ca²⁺ and Mg²⁺) over total cation strength, while SO₄ ^2? and Cl^? constitute the majority of total anion load. Higher value of Ca²⁺?+?Mg²⁺/Na⁺?+?K⁺ (pre-monsoon 5.986, monsoon 8.866, post-monsoon 7.09) and Ca²⁺?+?Mg²⁺/HCO₃ ^??+?SO ₄ ² (pre-monsoon 7.14, monsoon 9.57, post-monsoon 8.29) is explained by weathering of Ca?CMg silicates and dissolution of Ca²⁺-bearing minerals present in parent rocks and overburden materials. Silicate weathering supposed to be the major geological contributor, in contrast to bicarbonate weathering does a little. Distribution coefficient for dissolved metals and sorbed to surface sediments is in the order of Cd?>?Pb?>?Fe?>?Zn?>?Cu?>?Cr?>?Mn. Speciation study of monitored metals in surface sediments shows that Fe and Mn are dominantly fractionated in exchangeable-acid reducible form, whereas rest of the metals (Cr, Pb, Cd, Zn, and Cu) mostly in residual form. Cd, Pb, and Zn show relatively higher recalcitrant factor that indicates their higher retention in lake sediments. Factor loading of monitored physico-chemical parameters resembles contribution/influences from geological weathering, anthropogenic inputs as well as natural temporal factors. Ionic load/strength of lake water accounted for geochemical process and natural factors, while pollutant load (viz BOD, COD and metals, etc.) is associated with anthropogenic inputs through industrial discharge.     

Fluvial geochemistry of Subarnarekha River basin,India

The fluvial geochemistry of the Subarnarekha River and its major tributaries has been studied on a seasonal basis in order to assess the geochemical processes that explain the water composition and estimate solute fluxes. The analytical results show the mildly acidic to alkaline nature of the Subarnarekha River water and the dominance of \(\hbox {Ca}^{2+}\) and \(\hbox {Na}^{+}\) in cationic and \(\hbox {HCO}_{3}^{-}\) and \({\hbox {Cl}}^{-}\) in anionic composition. Minimum ionic concentration during the monsoon and maximum concentration in the pre-monsoon seasons reflect concentrating effects due to decrease in the river discharge and increase in the base flow contribution during the pre-monsoon and dilution effects of atmospheric precipitation in the monsoon season. The solute acquisition processes are mainly controlled by weathering of rocks, with minor contribution from marine and anthropogenic sources. Higher contribution of alkaline earth \((\hbox {Ca}^{2+}{+}\,\hbox {Mg}^{2+})\) to the total cations \((\hbox {TZ}^{+})\) and high \((\hbox {Na}^{+}+\hbox {K}^{+})/\hbox {Cl}^{-}\), \((\hbox {Na}^{+}+\hbox {K}^{+})/\hbox {TZ}^{+}\), \(\hbox {HCO}_{3}^{-}/(\hbox {SO}_{4}^{2-}+\hbox {Cl}^{-})\) and low \((\hbox {Ca}^{2+}+\hbox {Mg}^{2+})/(\hbox {Na}^{+}+\hbox {K}^{+})\) equivalent ratios suggest that the Subarnarekha River water is under the combined influence of carbonate and silicate weathering. The river water is undersaturated with respect to dolomite and calcite during the post-monsoon and monsoon seasons and oversaturated in the pre-monsoon season. The pH–log \(\hbox {H}_{4}\hbox {SiO}_{4}\) stability diagram demonstrates that the water chemistry is in equilibrium with the kaolinite. The Subarnarekha River annually delivered \(1.477\times 10^{6}\) ton of dissolved loads to the Bay of Bengal, with an estimated chemical denudation rate of \(77\hbox { ton km}^{-2}\hbox { yr}^{-1}\). Sodium adsorption ratio, residual sodium carbonate and per cent sodium values placed the studied river water in the ‘excellent to good quality’ category and it can be safely used for irrigation.     

Factor analysis in hydrogeochemistry of coastal aquifers – a preliminary study

 This paper examines the results of R-mode factor analysis performed on major ion data from a hydrogeochemical survey over the coastal Quaternary deltaic aquifer of the Cauvery Basin, Tamil Nadu, India. Seven major ions (Ca, Mg, Na, K, HCO₃, Cl, and NO₃) were analyzed from each of the 126 water samples collected in two seasons (pre- and post-monsoon 63 each). A set of factors was found both in pre-monsoon and post-monsoon data which explained the source of the dissolved ions and the chemical processes which accompany the intrusion of seawater. Received: 4 March 1996 · Accepted: 28 August 1996     

Geochemistry and assessment of hydrogeochemical processes in groundwater in the southern part of Bathinda district of Punjab, northwest India

Hydrogeochemistry of groundwater is important for sustainable development and effective management of the groundwater resource. Fifty-six groundwater samples were collected from shallow tube wells of the intensively cultivated southern part of district Bathinda of Punjab, India, during pre- and post-monsoon seasons. Conventional graphical plots were used to define the geochemical evaluation of aquifer system based on the ionic constituents, water types, hydrochemical facies and factors controlling groundwater quality. Negative values of chloroalkaline indices suggest the prevalence of reverse ion exchange process irrespective of the seasons. A significant effect of monsoon is observed in terms chemical facies as a considerable amount of area with temporary hardness of Ca²⁺–Mg²⁺–HCO₃ ^? type in the pre-monsoon switched to Ca²⁺–Mg²⁺–Cl^? type (18%) followed by Na⁺–HCO₃ ^? type (14%) in the post-monsoon. Evaporation is the major geochemical process controlling the chemistry of groundwater process in pre-monsoon; however, in post-monsoon ion exchange reaction dominates over evaporation. Carbonate weathering is the major hydrogeochemical process operating in this part of the district, irrespective of the season. The abundance of Ca²⁺ + Mg²⁺ in groundwater of Bathinda can be attributed mainly to gypsum and carbonate weathering. Silicate weathering also occurs in a few samples in the post-monsoon in addition to the carbonate dissolution. Water chemistry is deteriorated by land-use activities, especially irrigation return flow and synthetic fertilisers (urea, gypsum, etc.) as indicted by concentrations of nitrate, sulphate and chlorides. Overall, results indicate that different natural hydrogeochemical processes such as simple dissolution, mixing, weathering of carbonate minerals locally known as ‘‘kankar’’ and silicate weathering are the key factors in both seasons.     

南水北调中线水源地河水地球化学特征与流域侵蚀

丹江口水库及其上游流域是南水北调中线工程的水源地,本文讨论了水源地河流水化学与锶同位素(87Sr/86Sr)组成变化特征,目的在于了解水源地流域河流地表水溶质的物质来源以及岩石风化侵蚀过程和人为活动的影响。流域内河流水化学组成以Ca2+、HCO3-为主,Mg2+和SO42-次之,反映了碳酸盐岩风化溶解起控制作用的典型特征。水化学分析表明水源地河水受到工农业活动等人为因素的影响;河流87Sr/86Sr同位素地球化学研究表明,流域岩石风化输入至少存在三个不同端员(硅酸岩、石灰岩和白云岩)之间的混合。水源地流域内硅酸岩和碳酸岩的风化侵蚀速率分别为38.6和4.4 t/km2.a,总岩石风化侵蚀速率高于全球河流平均值。     

Major element chemistry of the Huai River basin, China

The chemistry of major ions (Ca, Mg, Na, K, HCO₃, SO₄, Cl and Si) in the water of the Huai River basin was studied, based on samples from 52 sites from nine different water bodies in July 2008. Ions and total dissolved solids (TDS) displayed clear spatial patterns with lower concentrations in the south and higher in the north of the basin; the same conditions were also found in the East Line of South-North Water Transfer Project (SNWTP) in this region. The Huai River main channel and Hongze Lake have moderate ion concentrations relative to the whole basin. TDS concentrations versus the weight ratios of Na/(Na + Ca) and ternary ions demonstrate that the southern rivers (Shi R. and Pi R.) are mainly controlled by the weathering of carbonates, whereas the northern water systems (Guo R., Shaying R., Nansi Lake and its tributaries) are dominated by the weathering of evaporites. The Huai River main channel, Hongze Lake and the East Line of SNWTP are synergistically influenced by weathering of evaporites and carbonates, yet Hongze Lake and the East Line of SNWTP are mainly controlled by evaporation and crystallization processes. This study also confirmed that the Huai River is the geographic division between southern and northern China. Most rivers of this basin have very high ionic composition relative to the global median and other world rivers. The spatial patterns and ionic composition also suggest that intensive anthropogenic activities in northern areas of this basin are well characterized. A comparison with WHO and Chinese standards for drinking water indicates that the northern water systems of this basin are not suitable for use as drinking water sources, and pollution control should be improved and enhanced in northern areas of the basin.     

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.     

Understanding the Cyclicity of Chemical Weathering and Associated CO<Subscript>2</Subscript> Consumption in the Brahmaputra River Basin (India): The Role of Major Rivers in Climate Change Mitigation Perspective

Weathering of rocks that regulate the water chemistry of the river has been used to evaluate the CO₂ consumption rate which exerts a strong influence on the global climate. The foremost objective of the present research is to estimate the chemical weathering rate (CWR) of the continental water in the entire stretch of Brahmaputra River from upstream to downstream and their associated CO₂ consumption rate. To establish the link between the rapid chemical weathering and thereby enhance CO₂ drawdown from the atmosphere, the major ion composition of the Brahmaputra River that drains the Himalaya has been obtained. Major ion chemistry of the Brahmaputra River was resolved on samples collected from nine locations in pre-monsoon, monsoon and post-monsoon seasons for two cycles: cycle I (2011–2012) and cycle II (2013–2014). The physico-chemical parameters of water samples were analysed by employing standard methods. The Brahmaputra River was characterized by alkalinity, high concentration of Ca²⁺ and HCO₃ ^? along with significant temporal variation in major ion composition. In general, it was found that water chemistry of the river was mainly controlled by rock weathering with minor contributions from atmospheric and anthropogenic sources. The effective CO₂ pressure (log\({{\text{P}}_{{\text{C}}{{\text{O}}_{\text{2}}}}}\)) for pre-monsoon, monsoon and post-monsoon has been estimated. The question of rates of chemical weathering (carbonate and silicate) was addressed by using TDS and run-off (mm year^?1). It has been found that the extent of CWR is directly dependent on the CO₂ consumption rate which may be further evaluated from the perspective of climate change mitigation The average annual CO₂ consumption rate of the Brahmaputra River due to silicate and carbonate weathering was found to be 0.52 (×10⁶ mol Km^?2 year^?1) and 0.55 (×10⁶ mol Km^?2 year^?1) for cycle I and 0.49 (×10⁶ mol Km^?2 year^?1) and 0.52 (×10⁶ mol Km^?2 year^?1) for cycle II, respectively, which were significantly higher than that of other Himalayan rivers. Estimation of CWR of the Brahmaputra River indicates that carbonate weathering largely dominates the water chemistry of the Brahmaputra River.     

Groundwater geochemistry of a small reservoir catchment in Central Tunisia

Due to the scarcity of water resources in semiarid sedimentary basins, hill reservoirs are often constructed to recharge groundwater and limit runoff induced water loss. The impact of such reservoirs on groundwater chemistry is investigated in the aquifers of the El Gouazine watershed, Central Tunisia. Three groundwater types are recognised, Ca–HCO₃, Na–Cl and Ca–SO₄. The strong similarity between host rock and groundwater chemistries indicates significant rock–water interaction. A flowpath, along which the chemical composition of the groundwater evolves, can be identified using the contrast in stable isotope signature between upstream and downstream groundwater. Shallow upstream groundwater is recharged by the infiltration of rainwater with the rate of recharge strongly linked to the permeability of the host lithology. Calcium and HCO₃ are supplied to an alluvial aquifer from a more rapidly recharged limestone aquifer with the concentration of Ca and HCO₃ ions decreasing by dilution. The alluvial aquifer is also enriched in Ca and SO₄ during the downstream flow of groundwater through gypsiferous materials. There is evidence of mixing between meteoric groundwater and evaporated reservoir water. Below the reservoir and partly responsible for reservoir leakage is a sandy aquifer, formed by weathering and erosion of a sandstone host which also supplies water to the alluvial aquifer.     

Tracing ionic sources and geochemical evolution of groundwater in the Intermountain Una basin in outer NW Himalaya,Himachal Pradesh,India

The present research aims to identify sources of ions and factors controlling the geochemical evolution of groundwater in an intermountain basin, comprising hill and valley fill region, of Outer Himalaya in Himachal Pradesh, India. The groundwater samples collected from 81 tubewells and handpumps are analyzed for major ions, trace metals and stable isotopes (δ¹⁸O and δD). Geochemically the dominant hydrochemical facies in the Una basin are Ca–HCO₃, Ca–Mg–HCO₃ and Na–Cl types at few locations. A relatively lower ionic concentration in the valley fills indicates dilution and low residence time of water to interact with the aquifer mass due to high porosity and permeability. The ionic ratios of 0.9, 0.8 and 3.8 to 5.7, respectively, for (Ca?+?Mg): HCO₃, (Ca?+?Mg): (HCO₃?+?SO₄) and Na: Cl, suggests that ionic composition of groundwater is mainly controlled by rock weathering of, particularly by dissolution/precipitation of calcrete and calcite hosted in rock veins and Ca–Na feldspar hosted in conglomerate deposits derived from the Higher and Lesser Himalaya during the formation of Siwalik rocks. Although Na, K, NO₃ and SO₄ are introduced in the groundwater through agricultural practices, Na has also been introduced through ion exchange processes that have occurred during water–rock interaction, as indicated by negative CAI values. Factor analysis further suggests three major factors affecting the water chemistry of the area. The first two factors are associated with rock weathering while the third is anthropogenic processes associated with high nitrate and iron concentration. High concentrations of Fe and Mn ions that are exceeded that of WHO and BIS standards are also present at few locations. The recharge of groundwater in the Outer Himalaya is entirely through Indian Southwest Monsoon (ISM) and depleted ratios of δ¹⁸O/δD in valley region indicate infiltration from irrigation in recharging the groundwater and fractionation of isotopes of precipitation due to evaporation before infiltration. High d-excess values and inverse relation with δ¹⁸O are indicative of secondary evaporation of precipitation during recharge of groundwater.