Assessing the hydrogeochemistry and water quality of the Aji-Chay River,northwest of Iran

Aji-Chay River is one of the most important surface reservoirs of northwest of Iran, because it passes through Tabriz city and discharges to Urmia Lake, one of the largest permanent salty lakes in the world. The main objectives of the present study are to evaluate its overall water quality and to explore its hydrogeochemical characteristics, including the potential contamination from heavy metals and metalloids such as Co, Pb, Zn, Cd, Cu, Cr, Al and As. For this purpose, 12 water samples were collected from the main river body and its tributaries within Tabriz plain. The Piper diagram classified water samples mainly into Na–Cl and secondary into Ca–HCO₃ and mixed Ca–Mg–Cl types, denoting a profound salinization effect. The cross-plots showed that natural geochemical processes including dissolution of minerals (e.g., carbonates, evaporites and silicates), as well as ion exchange, are the predominant factors that contribute to fluvial hydrogeochemistry, while anthropogenic activities (industrial and agricultural) impose supplementary effects. Cluster analysis classified samples into two distinct clusters; samples of cluster B appear to have elevated electrical conductivity (EC) values and trace metals concentrations such as Co, Pb and Cd, while SiO₂ and Zn are low in comparison with the samples of the cluster A. The main processes controlling Aji-Chay River hydrogeochemistry and water quality were identified to be salinization and rock weathering. Both are related with geogenic sources which enrich river system with elevated values of Na⁺, Cl^?, Ca²⁺, Mg²⁺, K⁺, SO₄ ^2? and EC as a direct effect of evaporites leaching and elevated values of Pb and Cd as an impact from the weathering process of volcanic formations. According to the US salinity diagram, all of the water samples are unsuitable for irrigation as having moderate to bad quality.     

Seasonal and spatial variations in water chemistry and nitrate sources in six major Korean rivers

Seasonal and spatial variations in water chemistry and contaminant sources were investigated in six major rivers in South Korea that vary widely in drainage area and length. The dissolved-load content of the rivers varied seasonally, and some dissolved ions such as Cl^? and NO₃ ^? showed large spatial differences in all of the rivers. The water type changed from Ca–HCO₃ in the upper reaches to Na–Cl–NO₃ in the lower reaches, indicating anthropogenic contamination in the lower reaches. Compared with two relatively pristine rivers (the Sumjin and Mankyung rivers), the other four rivers, which flow through agricultural and urban areas, registered much higher Cl^? and NO₃ ^? concentrations. Statistical analysis showed that seasonal and spatial variations in water chemistry occurred in all the rivers. The nitrogen and oxygen isotopes of dissolved nitrate indicated that the rivers flowing through urban and agricultural areas were significantly affected by manure, sewage, or both.     

Evaluating the influence of road salt on water quality of Ohio rivers over time

Anthropogenic inputs have largely contributed to the increasing salinization of surface waters in central Ohio, USA. Major anthropogenic contributions to surface waters are chloride (Cl⁻) and sodium (Na⁺), derived primarily from inputs such as road salt. In 2012–2013, central Ohio rivers were sampled and waters analyzed for comparison with historical data. Higher Cl⁻ and Na⁺ concentrations and fluxes were observed in late winter as a result of increased road salt application during winter months. Increases in both chloride/bromide (Cl⁻/Br⁻) ratios and nitrate (N-NO₃⁻) concentrations and fluxes were observed in March 2013 relative to June 2012, suggesting a mixture of road salt and fertilizer runoff influencing the rivers in late winter. For some rivers, increased Cl⁻ and Na⁺ concentrations and fluxes were observed at downstream sites near more urban areas of influence. Concentrations of Na⁺ were slightly lower than respective Cl⁻ concentrations (in equivalents). High Cl⁻/Br⁻ mass ratios in the Ohio surface waters indicated the source of Cl⁻ was likely halite, or road salt. In addition, analysis of ³⁶Cl/Cl ratios revealed low values suggestive of a substantial dissolved halite component, implying the addition of “old” Cl⁻ into the water system. Temporal trend analysis via the Mann–Kendall test identified increasing trends in Cl⁻ and Na⁺ concentration beginning in the 1960s at river locations with more complete historical datasets. An increasing trend in Cl⁻ flux through the 1960s was also identified in the Hocking River at Athens, Ohio. Our results were similar to other studies that examined road salt impacts in the northern US, but a lack of consistent long-term data hindered historical analysis for some rivers.     

Sources of dissolved ions revealed by chemical and isotopic tracers in the Geum River,South Korea

Water samples were collected in the main channel of the Geum River, South Korea, and measured dissolved elemental concentrations and isotopic compositions of nitrate in order to identify the factors controlling water chemistry. Elemental concentrations significantly increased location-wise after the confluence from urban areas, indicating the changes in solute sources from chemical weathering to anthropogenic inputs such as manure, fertilizers, and sewage. In particular, the effect of sewage input is manifested in the concentrations of Cl^?, SO₄ ^2?, and Na⁺, while the NO₃ ^? concentration is influenced mainly by soil inputs with minor contributions from manure and fertilizer because both δ¹⁵N–NO₃ and δ¹⁸O–NO₃ indicate NO₃ ^? mostly consists of soil-derived nitrates in the upper reaches but manure/sewage nitrates in the lower reaches. The relative proportion of three factors, Cl^?, Ca²⁺+Mg²⁺, and NO₃ ^?, indicates that water chemistry in the upstream is controlled by the soil weathering but that in the downstream by the sewage. Seasonally, water chemistry during summer is dominated by the soil weathering due to the flushing effect but that during winter by the sewage. This study suggests that the relative proportion of three factors can be used for tracing natural and anthropogenic sources in water chemistry.     

Characterization of hydrogeochemical process and evaluation of water quality of seven geothermal springs,Bakreswar, India

A study was conducted in seven geothermal springs located in Bakreswar, District Birbhum, West Bengal, India, in order to assess numerous geochemical processes which were responsible for chemical composition of thermal and mineralized water. The study area lies over the Sone, Narmada, and Tapti lineament of Precambrian Chotanagpur Gneissic Complex. Water chemistry has been carried out based on reaction stoichiometry and geo-statistical tools to identify geochemical process. Piper and Gibbs diagram suggest that the spring water belongs to Ca²⁺-Mg²⁺-HCO₃^??+?CO₃^2? water type and are controlled by rock dominance. Dissolution and precipitation of calcite, dolomite, gypsum, and fluorite minerals were identified as principle source of major ions in seven geothermal spring water. Principle component analyses revealed that major ions of spring water are derived from geogenic processes such as weathering, dissolution, and precipitation of various minerals. Overall results suggest that major ions of the spring’s water are derived from natural origin because no evidence of anthropogenic sources was observed during the study period. This study has also revealed that water quality of spring’s water is not suitable for drinking purposes and quite suitable for irrigation because of high abundance of Na⁺, K⁺, Cl^?, and HCO₃^? ions.     

Multivariate water quality assessment from the Tamiraparani river basin,Southern India

The hydrochemistry of a perennial river has been investigated with multivariate cluster analysis (CA) and principal component analysis/factor analysis (PCA/FA). The aim was to investigate parameters responsible for spatial and temporal variations of river water quality. Water quality was monitored along the river basin at 20 different sites over a period of 1 year from July, 2008 to June, 2009. Multivariate statistics revealed that Ca²⁺, Mg²⁺, Na⁺, K⁺, HCO₃ ^?, Cl^?, H₄SiO₄, SO₄ ^2?, NO₂ ^?, and PO₄ ^3? were influenced by seasonal and spatial variations and that water quality was in the first place determined more by natural weathering processes than by anthropogenic activities. We could prove by (a) Box and Whisker plot, (b) matrix scatter score mean plot, (c) ternary plot, and (d) Gibbs plot that the chemistry of river water is controlled by lithogenic weathering processes. The higher concentration of dissolved silica during summer and the pre-monsoon season is explained by natural and tropical climatic conditions of the environment.     

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

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

Assessment of the quality of groundwater from different parts of southeastern Nigeria for potable use

Groundwater samples from three different states of southeastern Nigeria were analyzed for a range of physicochemical parameters and heavy metal constituents in order to determine their potability as drinking water sources. The results indicate that the physicochemical parameters (pH, temperature, TDS, TH, electrical conductivity, Cl^?, NO₃ ^? and SO₄ ^2?) tested for have most of their values fall within the permissible limits given by the Nigerian and World Health Organization standards for drinking water quality. The results also reveal that apart from Cu and Pb the rest of the tested heavy metals (As, Zn, Ni, total Fe, Cd and Mn) recorded values that are significantly above the maximum permissible limits for drinking water purposes and therefore have the potential to cause health impacts for long-term potable use. On the basis of principal component analysis, the sources of the measured chemical constituents are likely to be predominantly geogenic (weathering of soluble minerals in the formations) and partly anthropogenic (industrial effluent, agricultural practices and mining activities). Single-factor ANOVA tests indicated insignificant differences in the datasets within/between states or geological units. Caution or adequate treatment is generally required when utilizing the groundwater from the area for drinking purpose due to the elevated metal concentrations and rating as poor to unsuitable water quality.     

Groundwater solute chemistry,hydrogeochemical processes and fluoride contamination in phreatic aquifer of Odisha,India

The work investigates the major solute chemistry of groundwater and fluoride enrichment(F~-) in the shallow phreatic aquifer of Odisha.The study also interprets the hydrogeochemical processes of solute acquisition and the genetic behavior of groundwater F~-contamination.A total of 1105 groundwater samples collected from across the state from different hydro-geomorphic settings have been analyzed for the major solutes and F~-content.Groundwater is alkaline in nature(range of pH: 6.6–8.7; ave.: 7.9) predominated by moderately hard to very hard types.Average cation and anion chemistry stand in the orders of Ca~(2+) Na~+ Mg~(2+) K~+and HCO_3~- Cl~- SO_4~(2-) CO_3~(2-)respectively.The average mineralization is low(319 mg/L).The primary water types are Ca-Mg-HCO_3 and Ca-Mg-Cl~-HCO_3, followed by Na-Cl, Ca-Mg-Cl, and Na-Ca-Mg-HCO_3~-Cl.Silicate-halite dissolution and reverse ion exchange are the significant processes of solute acquisition.Both the geogenic as well as the anthropogenic sources contribute to the groundwater fluoride contamination,etc.The ratio of Na~+/Ca~(2+) 1.0 comprises Na-HCO_3(Cl) water types with F~- 1.0 mg/L(range 1.0–3.5 mg/L)where the F~-bears geogenic source.Positive relations exist between F~-and pH, Na~+, TDS, and HCO_3~-.It also reflects a perfect Na-TDS correlation(0.85).The ratio of Na~+/Ca~(2+) 1.0 segregates the sample population(F~- range: 1.0–4.0 mg/L) with the F derived from anthropogenic sources.Such water types include Ca-Mg-HCO_3(Cl) varieties which are recently recharged meteoritic water types.The F~-levels exhibit poor and negative correlations with the solutes in groundwater.The Na-TDS relation remains poor(0.12).In contrast, the TDS levels show strong correlations with Ca~(2+)(0.91), Mg~(2+)(0.80) and even Cl~-(0.91).The majority of the monitoring points with the anthropogenic sources of groundwater F~-are clustered in the Hirakud Canal Command area in the western parts of the state, indicating the role of irrigation return flow in the F~-contamination.     

Assessment of hydrogeochemical processes in a coastal region: Application of multivariate statistical model

Hydrogeochemical studies have been carried out in a coastal region, using multivariate statistical model, for better understanding the controlling processes that influence the aquifer chemistry. Two principal components (PC1 and PC2) are extracted from the data set of chemical variables (pH, TDS, Ca²⁺, Mg²⁺, Na⁺, K⁺, HCO ₃ ^? , Cl^?, SO ₄ ^2? , NO ₃ ^? and F^?), which account for 79% of the total variation in the quality of groundwater. The PC1 (salinity controlled process) includes the concentrations of TDS, Mg²⁺, Na⁺, K⁺, Cl^?, SO ₄ ^2? and NO ₃ ^? , while the PC2 (alkalinity controlled process) comprises the concentrations of pH, HCO ₃ ^? and F^?. The spatial distribution of PC scores identifies the locations of high salinity and alkalinity processes. The first process corresponds to the influences of geogenic, anthropogenic and marine sources, and the second one to the influence of water-soil-rock interaction. Thus, the present study shows the usefulness of multivariate statistical model as an effective means of interpretation of spatial controlling processes of groundwater chemistry.     

Hydrogeochemical processes and quality assessment of groundwater in Dumka and Jamtara districts, Jharkhand, India

The hydrogeochemical study of groundwater in Dumka and Jamtara districts has been carried out to assess the major ion chemistry, hydrogeochemical processes and groundwater quality for domestic and irrigation uses. Thirty groundwater samples were collected and analyzed for pH, electrical conductivity, total dissolved solids (TDS), total hardness, anions (F^?, Cl^?, NO₃ ^?, HCO₃ ^?, SO₄ ^2?) and cations (Ca²⁺, Mg²⁺, Na⁺, K⁺). The analytical results show the faintly alkaline nature of water and dominance of Mg²⁺ and Ca²⁺ in cationic and HCO₃ ^? and Cl^? in anionic abundance. The concentrations of alkaline earth metals (Ca²⁺?+?Mg²⁺) exceed the alkali metals (Na⁺?+?K⁺) and HCO₃ ^? dominates over SO₄ ^2??+?Cl^? concentrations in the majority of the groundwater samples. Ca?CMg?CHCO₃ is the dominant hydrogeochemical facies in 60?% of the groundwater samples, while 33?% samples occur as a mixed chemical character of Ca?CMg?CCl hydrogeochemical facies. The water chemistry is largely controlled by rock weathering and ion exchange processes with secondary contribution from anthropogenic sources. The inter-elemental correlations and factor and cluster analysis of hydro-geochemical database suggest combined influence of carbonate and silicate weathering on solute acquisition processes. For quality assessment, analyzed parameter values were compared with Indian and WHO water quality standards. In majority of the samples, the analyzed parameters are well within the desirable limits and water is potable for drinking purposes. Total hardness and concentrations of TDS, Cl^?, NO₃ ^? _, Ca²⁺ and Mg²⁺ exceed the desirable limits at a few sites, however, except NO₃ ^? all these values were below the highest permissible limits. The calculated parameters such as sodium adsorption ratio, percent sodium (%Na) and residual sodium carbonate revealed excellent to good quality of groundwater for agricultural purposes, except at few sites where salinity and magnesium hazard (MH) values exceeds the prescribed limits and demands special management.     

Seasonal and spatial water quality changes in the outflow plume of the Atchafalaya River,Louisiana, USA

The objective of this study was to examine the interaction between the Atchafalaya River and the Atchafalaya Delta estuarine complex. Measurements of suspended sediments, inorganic nutrients (NO₃ ^?, NH₄ ⁺, PO₄ ^3?), chlorophylla (chla), and-salinity were taken monthly from December 1996 to January 1998. These data were compiled by season, and the Atchafalaya River plume data were also analyzed using the Generalized Additive Model technique. There were significant decreases in NO₃ ^? concentrations during summer, fall, and winter as river water passed through the estuary, that were attributable to chemical and biological processes rather than dilution with ambient water. In some regions there were higher chla concentrations during summer and fall compared to winter and spring, when river discharge and the introduction of inorganic nutrients were highest, suggesting biological processes were active during this study. The presence of NH₄ ⁺, as a percentage of available dissolved inorganic nitrogen, increased with distance from the Atchafalaya River, indicative of remineralization processes and NO₃ ^? reduction. Mean PO₄ ^3? concentrations were often higher in the estuarine regions compared to the Atchafalaya River. During summer total suspended solid (TSS) concentrations increased with distance from the river mouth, suggesting a turbidity maximum. Highest chla concentrations were found in the bayous and shallow water bodies of the Terrebonne marshes, as were the lowest TSS concentrations. The low chla concentrations found in other areas of this study, despite high inorganic nutrient concentrations, suggest light limitation as the major control of phytoplankton growth. Salinity reached near seawater concentrations at the outer edge of the Atchafalaya River plume, but much lower salinities (<10 psu) were observed at all other regions. The Atchafalaya Delta estuarine complex buffers the impact of the Atchafalaya River on the Louisiana coastal shelf zone, with a 41% of 47% decrease in Atchafalaya River NO₃ ^? concentrations before reaching Gulf waters.     

Hydrogeochemical investigation and groundwater quality assessment of Pratapgarh district,Uttar Pradesh

Hydogrochemical investigation of groundwater resources of Paragraph district has been carried out to assess the solute acquisition processes and water quality for domestic and irrigation uses. Fifty-five groundwater samples were collected and analyzed for pH, electrical conductivity, total dissolved solids, hardness, major anions (F^?, Cl^?, NO₃, HCO₃ ^?, SO₄ ^2?) and cations (Ca²⁺, Mg²⁺, Na⁺, K⁺). Study results reveal that groundwater of the area is alkaline in nature and HCO₃ ^?, Cl^?, Mg²⁺, Na⁺ and Ca²⁺ are the major contributing ions to the dissolved solids. The hydrogeochemical data suggest that weathering of rock forming minerals along with secondary contributions from agricultural and anthropogenic sources are mainly controlling the groundwater composition of Pratapgarh district. Alkaline earth metals (Ca²⁺+Mg²⁺) exceed alkalis (Na⁺+K⁺) and weak acid (HCO₃ ^?) dominate over strong acids (Cl^?+SO₄ ^2?) in majority of the groundwater samples. Ca-Mg-HCO₃ and Ca-Mg-Cl-HCO₃ are the dominant hydrogeochemical facies in the groundwater of the area. The computed saturation indices demonstrate oversaturated condition with respect to dolomite and calcite and undersaturated with gypsum and fluorite. A comparison of groundwater quality parameters in relation to specified limits for drinking water shows that concentrations of TDS, F^?, NO₃ ^? and total hardness exceed the desirable limits in many water samples. Quality assessment for irrigation uses reveal that the groundwater is good for irrigation. However, values of salinity, sodium adsorption ratio (SAR), residual sodium carbonate (RSC), %Na and Kelley index are exceeding the prescribed limit at some sites, demanding adequate drainage and water management plan for the area.     

Hydrochemical characteristics and quality assessment of regolith aquifers in Enugu metropolis, southeastern Nigeria

Twenty groundwater samples were collected from Enugu metropolis over two seasonal periods in order to characterize the groundwater and to determine its quality for domestic and irrigation purposes. The results show that groundwater of the area is strongly acidic to slightly alkaline in nature and varied from “soft water” to “moderately hard” water type. The major ionic trend is in the order Cl^? > Na⁺ > HCO₃ ^? > K⁺ > Mg²⁺ > Ca²⁺ > SO₄ ^2?and Mg²⁺ > Cl^? > Na⁺ > K⁺ > Ca²⁺ > HCO ₃ ^?  > SO₄ ^2? in abundance for dry and rainy seasons, respectively. The results also reveal that there is an increase in trend of the ionic concentrations during the dry season, which arises from weathering of the host rocks and anthropogenic activities. Two hydrochemical facies were identified, namely, Na⁺ –K⁺ –Cl^? –SO₄ ^2?and Ca²⁺ –Mg²⁺ –Cl^? –SO₄ ^2? _, with Na⁺ –K⁺ –Cl^? –SO₄ ^2? as the dominant facies for the two seasons. Groundwater quality ranges from “very poor water” to “good water” and “water unsuitable for drinking purposes” to “good water” for the dry season and rainy season investigations, respectively. The groundwater is suitable for irrigation purposes for the two seasons.     

Surface water chemistry and nitrate pollution in Shimabara,Nagasaki, Japan

Groundwater is a finite resource that is threatened by pollution all over the world. Shimabara City, Nagasaki, Japan, uses groundwater for its main water supply. During recent years, the city has experienced severe nitrate pollution in its groundwater. For better understanding of origin and impact of the pollution, chemical effects and surface–groundwater interactions need to be examined. For this purpose, we developed a methodology that builds on joint geochemical analyses and advanced statistical treatment. Water samples were collected at 42 sampling points in Shimabara including a part of Unzen City. Spatial distribution of water chemistry constituents was assessed by describing Stiff and Piper diagrams using major ions concentrations. The nitrate (NO₃?+?NO₂–N) concentration in 45% of water samples exceeded permissible Japanese drinking level of 10 mg L^??1. Most of the samples showed Ca–HCO₃ or Ca–(NO₃?+?SO₄) water types. Some samples were classified into characteristic water types such as Na–Cl, (Na?+?K)–HCO₃, (Na?+?K)–(SO₄?+?NO₃), and Ca–Cl. Thus, results indicated salt water intrusion from the sea and anthropogenic pollution. At the upstream of Nishi River, although water chemistry was characterized as Ca–HCO₃, ion concentrations were higher than those of other rivers. This is probably an effect of disinfection in livestock farming using slaked lime. Positive correlation between NO₃^? and SO₄^2?, Mg²⁺, Ca²⁺, Na⁺, K⁺, and Cl^? (r?=?0.32–0.64) is evidence that nitrate pollution sources are chemical fertilizers and livestock waste. Principal component analysis showed that chemistry of water samples can be explained by three main components (PCs). PC1 depicts general ion concentration. PC2 and PC3 share influence from chemical fertilizer and livestock waste. Cluster analyses grouped water samples into four main clusters. One of these is the general river chemistry mainly affected by PC1. The others reflect anthropogenic activities and are identified by the combination of the three PCs.     

Groundwater contamination in parts of Nalgonda district,Telangana, India as revealed by trace elemental studies

The present paper deals with major and trace elements geochemistry of the groundwater from Nalgonda district, Telangana. The study area is very important in terms of anthropogenic activity like rapid industrial, urban development, pesticides, pharmaceutical, granite polishing and agro based industries. Inductively coupled plasma mass spectrometer (ICPMS) was employed to determine the concentration of trace elements in collected groundwater samples (bore well). These probe elements were further categorized as toxic elements (Pb, As, Cd, and V), alkaline earths (Sr and Ba), alkali metals (Li, Rb), transition metals (Cr, Mo and Ni), metallic elements (Cu, Fe, Zn, Al, Co), and other non-metallic elements (Se and Si). The groundwater quality was examined in perspective of Indian as well as World Health Organization drinking water standards. Based on the analytical results, groundwater in the study area is found to be slightly alkaline in nature and very hard, the average abundance of the major cations and anions is in the order of Ca⁺<Na⁺<Mg⁺<K⁺ and Cl^-<HCO₃ ^?<CO₃ ^?<SO₄ ^?<NO₃ ^?<F^– respectively. The dominant hydro chemical facies of groundwater is Na⁺ - HCO ₃ ^– – Cl^– and Na⁺ - Cl^– – HCO^– ₃ types.The results of trace elements shows that concentration of Pb, As, Cd, V in collected samples exceeding the desirable limits, and in the case of alkaline, alkali, transition, non-metallic elements, seventy per cent of the samples crossed the desirable limits, but all metallic elements viz. Cu, Fe, Zn, Al, Co is within the limits as per Indian as well as World Health Organizations drinking water standards. Factor analysis results shows that seven factors emerged as a significant contributor to the groundwater contamination is about 65.32 per cent. The spatial variation maps decipher trace elemental concentrations both geogenic and anthropogenic origin, by three zones i.e. ‘low’, ‘moderate’ and ‘high’ of the study area based on environment using Arc-GIS. High concentrations of trace elements are indicative of phenomenal rise in chemical composition and likely to have its origin from silicate weathering reactions and dissolution/precipitation processes supported by rainfall and anthropogenic activities, indiscriminate use of fertilizers/pesticides, and disposal of waste and sewage, release of reactive pollutants into the atmosphere by industries. Hence, this work is of immense societal benefit in terms of prevailing human health hazards in the study area with a direct relevance to such industrially populated regions elsewhere.     

Environmental geochemistry and quality assessment of surface and subsurface water of Mahi River basin, western India

The hydrogeochemical study of surface and subsurface water of Mahi River basin was undertaken to assess the major ion chemistry, solute acquisition processes and water quality in relation to domestic and irrigation uses. The analytical results show the mildly acidic to alkaline nature of water and dominance of Na⁺ and Ca²⁺ in cationic and HCO₃ ⁻ and Cl⁻ in anionic composition. In general, alkaline-earth elements (Ca²⁺ + Mg²⁺) exceed alkalis (Na⁺ + K⁺) and weak acids (HCO₃ ⁻) dominate over strong acids (SO₄ ²⁺ + Cl⁻) in majority of the surface and groundwater samples. Ca²⁺–Mg²⁺–HCO₃ ⁻ is the dominant hydrochemical facies both in surface and groundwater of the area. The weathering of rock-forming minerals mainly controlled the solute acquisition process with secondary contribution from marine and anthropogenic sources. The higher concentration of sodium and dissolved silica, high equivalent ratios of (Na⁺ + K⁺/TZ⁺), (Na⁺ + K⁺/Cl⁻) and low ratio of (Ca²⁺ + Mg²⁺)/(Na⁺ + K⁺) suggest that the chemical composition of the water is largely controlled by silicate weathering with limited contribution from carbonate weathering and marine and anthropogenic sources. Kaolinite is the possible mineral that is in equilibrium with the water, implying that the chemistry of river water favors kaolinite formation. Assessment of water samples for drinking purposes suggests that the majority of the water samples are suitable for drinking. At some sites concentrations of TDS, TH, F⁻, NO₃ ⁻ and Fe are exceeding the desirable limit of drinking. However, these parameters are well within the maximum permissible limit except for some cases. To assess the suitability for irrigation, parameters like SAR, RSC and %Na were calculated. In general, both surface and groundwater is of good to suitable category for irrigation uses except at some sites where high values of salinity, %Na and RSC restrict its uses.     

Hydrochemical characteristics of groundwater and surface water for domestic and irrigation purposes in Vea catchment,Northern Ghana

The Vea catchment, mainly underlain by crystalline basement rocks, is located in Northern Ghana. Hydrogeochemical studies were carried out in this area with the objective of identifying the geochemical processes influencing water quality and suitability of surface and groundwater for agricultural and domestic uses. Sixty-one groundwater and four surface water samples were collected from boreholes, dams and rivers and analysed for Ca²⁺, Mg²⁺, Na⁺, K⁺, HCO₃ ^?, Cl^?, and SO₄ ^2?, Fe_tot, PO₄ ^3?, Mn_tot, NH₄ ⁺, NO₃ ^?, NO₂ ^?. In addition, pH, total dissolved solids, electrical conductivity, total hardness, turbidity, colour, salinity and dissolved oxygen were analysed. Chloro-alkaline indices 1 and 2, and characterization of weathering processes suggest that the chemistry of groundwater is dominated by the interaction between water and rocks. Cation exchange and silicate weathering are the dominant processes controlling the chemical composition of the groundwater in the area studied. Mineral saturation indices indicate the presence of at least three groups of groundwater in the Vea catchment with respect to residence time. The meteoric genesis index suggests that 86% of the water samples belong to the shallow meteoric water percolation type. The findings further suggest that the groundwater and surface water in the basin studied are mainly Ca–Mg–HCO₃ water type, regardless of the geology. Compared to the water quality guidelines of WHO, the study results on sodium absorption ratio, sodium percentage, magnesium hazard, permeability index and residual sodium carbonate indicate that groundwater and surface water in the Vea catchment are generally suitable for drinking and irrigation purposes.     

Origin and mobility of hexavalent chromium in North-Eastern Attica,Greece

An integrated framework that is comprised of field surveys of groundwater, surface water and soils, laboratory process experiments and hydrologic and geochemical modeling is used to identify the origin (anthropogenic versus geogenic sources), fate and transport of hexavalent Cr in Tertiary and Quaternary deposits of Oropos plain in Greece. Groundwater and soils were analyzed in May 2008 and exhibited considerable Cr concentrations. Mineralogical analysis and micro-XRF analysis of the heavy soil fractions (metallic components) showed Cr bearing phases like chromites, Cr-silicate phases with positive correlation between Si, Al, Fe and Cr soil concentrations. Column experiments showed the Cr(VI) desorption ability of soils, e.g. concentration of 20 μg L⁻¹ was detected after the application of 50 mm of rain. The groundwater model simulated the variability of Cr concentrations emanating from both anthropogenic and geogenic sources, successfully using rate constants obtained from the laboratory experiments, e.g. 4.24 nM h⁻¹ for serpentine soil and 0.77 nM h⁻¹ for soil in alluvial deposits. The mineralogical and geochemical results support a geogenic origin for Cr in soils and groundwater of Oropos plain while modeling results suggest that contaminants transported by Asopos River have affected only the upper layers of the subsurface in the vicinity of the river. The framework can be used to establish background concentrations or clean up levels of Cr-contaminated soils and groundwater.     

A study of groundwater irrigation water quality in south-central Bangladesh: a geo-statistical model approach using GIS and multivariate statistics

Southern Bangladesh’s irrigation and drinking water is threatened by saline intrusion. This study aimed to establish an irrigation water quality index (IWQI) using a geostatistical model and multivariate indices in Gopalganj district, south-central Bangladesh. Groundwater samples were taken randomly (different depths) in two seasons (wet-monsoon and dry-monsoon). Hydrochemical analysis revealed groundwater in this area was neutral to slightly alkaline and dominating cations were Na⁺, Mg²⁺, and Ca²⁺ along with major anions Cl^? and HCO₃ ^?. Principal component analysis and Gibbs plot helped explain possible geochemical processes in the aquifer. The irrigation water evaluation indices showed: electrical conductivity (EC) >750 µS/cm, moderate to extreme saline; sodium adsorption ratio (SAR), excellent to doubtful; total hardness (TH), moderate to very hard; residual sodium bicarbonate, safe to marginal; Kelly’s ratio >1; soluble sodium percentage (SSP), fair to poor; magnesium adsorption ratio, harmful for soil; and IWQI, moderate to suitable. In addition, the best fitted semivariogram for IWQI, EC, SAR, SSP, and TH confirmed that most parameters had strong spatial dependence and others had moderate to weak spatial dependence. This variation might be due to the different origin/sources of major contributing ions along with the influence of variable river flow and small anthropogenic contributions. Furthermore, the spatial distribution maps for IWQI, EC, SSP, and TH during both seasons confirmed the influence of salinity from the sea; low-flow in the major river system was the driving factor of overall groundwater quality in the study area. These findings may contribute to management of irrigation and/or drinking water in regions with similar groundwater problems.