Evidence for the occurrence of hydrogeochemical processes in the groundwater of Khoy plain,northwestern Iran,using ionic ratios and geochemical modeling

Rapid population growth, industrialization, and agricultural expansion in the Khoy area (northwestern Iran) have led to its dependence on groundwater and degradation of groundwater quality. This study attempts to decipher the major processes and factors that degrade the groundwater quality of the Khoy plain. For this purpose, 54 groundwater samples from unconfined and confined aquifers of the plain were collected in July 2017 and analyzed for major cations and anions (Na, K, Ca, Mg, HCO₃, SO_4, and Cl), minor ions (NO₃ and F), and Al. Magnesium and bicarbonate were identified as the dominant cation and anion, respectively. Several ionic ratios and geochemical modeling using PHREEQC indicated that the most important hydrogeochemical processes to affect groundwater quality in the plain were weathering and dissolution of evaporitic and silicate minerals, mixing, and ion exchange. There were smaller effects from evaporation and anthropogenic factors (e.g., industries). Results showed that the high salinity of the groundwater in the northeast area of the plain was due to the high solubility of the evaporitic minerals, e.g., halite and gypsum. Reverse ion exchange and the contribution of mineral dissolution were more significant than ion exchange in the northeastern part of the plain. Elevated salinity of the groundwater in the southeast was attributed mostly to reverse ion exchange and somewhat to evaporation.     

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.     

Geochemical and hydrogeochemical evolution of groundwater in Ferdows area, northeast of Iran

The chemical analysis of 19 water wells in Ferdows area, Northeastern Iran, has been evaluated to determine the hydrogeochemical processes and ion concentration background in the region. In the study area, the order of cation and anion abundance is Na⁺ > Ca²⁺ > Mg²⁺ > K⁺ and Cl^? > SO ₄ ^?2  > HCO₃ ^? > NO₃ ^?, respectively, and the dominating hydrochemical types are Na–Cl. Most metal concentrations in water depend on the mineral solubility, and pH, Eh, and salinity of the solution. Their ΣREE concentrations showed excellent correlations with parameters such as TDS and pH. North American Shale Composite (NASC)-normalized REE patterns are enriched in the HREEs relative to the LREEs for all groundwaters. They all have positive Eu anomalies (Eu/Eu* = 0.752–3.934) and slightly negative Ce anomalies (Ce/Ce* = 0.019–1.057). Reduction–oxidation, complexation, desorption, and re-adsorption alter groundwater REE concentrations and fractionation patterns. The positive Eu anomalies in groundwaters are probably due to preferential mobilization of Eu²⁺ relative to the trivalent REEs in the reducing condition.     

Multivariate statistics and hydrogeochemical modeling for source identification of major elements and heavy metals in the groundwater of Qareh-Ziaeddin plain,NW Iran

The present study aims to evaluate the possible source of major and some minor elements and heavy metals in the groundwater of Qareh-Ziaeddin plain, NW Iran with respect to chemical elements, saturation index, and multivariate statistics including correlation coefficient, cluster analysis, and factor analysis. Groundwater samples were collected in Jun 2016 and measured with respect to EC, pH, major and some minor elements and heavy metals including Fe, Mn, Zn, Cr, Pb, Cd, Al, and As. Among all the measured parameters, some of the samples exceed the World Health Organization (WHO) guideline value for EC, Na, Mg, HCO₃, SO₄, Cl, NO₃, F, As, Zn, and Pb. The results of correlation analysis show that weathering and dissolution of minerals especially evaporites and silicates, water-rock interaction, and cation exchange are dominant occurred processes in the groundwater of the study area. Also, denitrification process is occurred in the groundwater system. Cluster analysis categorizes the samples into three distinct groups which are different based on their EC and dependent variables, e.g., Na, Ca, Cl, SO₄ and pH, Pb, Cd, and As. It can be found that volcanic, evaporite, and clay formations have the least impact on the chemistry of the cluster 1 samples while clay and evaporite formations have the highest impact on the cluster 3 and also calcareous formations on cluster 2. Factor analysis shows that five factors, with total variance of 83%, are effective in the release of heavy metals and groundwater chemistry which are mostly geogenic.     

Geochemical and quality assessment of groundwater of Marand Basin, East Azarbaijan Province, northwestern Iran

The chemical analysis of 83 water wells in the Marand area, Azarbaijan Province NW of Iran was evaluated to determine the hydrogeochemical processes and ion concentration background in the region. Over the entire area, the dominated hydrochemical types are Ca? +?Mg?+?SO₄?+?Cl, Ca?+?SO₄, Na?+?Cl and Ca?+?Mg?+?HCO₃. Based on the total hardness, the softness of the groundwater is determined. According to electrical conductivity (EC) and sodium adsorption ratio (SAR), the most dominant classes are C3?CS1, C3?CS2, C4?CS2 and C2?CS1. The major ion concentrations are below the acceptable level for drinking water. The groundwater salinity hazard is medium to high, but the Na hazard is low to medium; with regard to irrigation water, the quality is low to medium. So, a drainage system is necessary to avoid the increase of toxic salt concentrations.     

Origin of groundwater salinity in the Fasa Plain,southern Iran,hydrogeochemical and isotopic approaches

The study area, the Fasa Plain, is situated in the semiarid region of Fars Province in the south of Iran. The Salloo diapir is a salt dome that crops out in the northwest of the study area. Isotopic and hydrochemical analyses were used to examine the water and how the origin of salinity and the diapir affect the quality of the groundwater quality in the study area. Groundwater was sampled from 31 representative pumping wells in alluvial aquifer and five springs in order to measure their stable isotope compositions, bromide ion concentration, and physical and chemical parameters. The alluvial aquifer was organized into two main groups based on the chemistry, with Group 1 consisting of low-salinity well samples (544–1744 µS/cm) with water type Ca–Mg–HCO₃–SO₄ which were taken in the center and north of the area, and Group 2 consisting of high-salinity samples (2550–4620 µS/cm) with water type Ca–Mg–Cl–SO₄ which were taken from the wells in the south and southwest of the area. A saline spring near the salt dome with an EC of 10,280 µS/cm has water type Na–Cl, while the compositions of the water in the other karstic springs is comparable to the fresh groundwater samples. All groundwater samples are undersaturated with respect to gypsum, anhydrite, and halite and are supersaturated with respect to calcite and dolomite. Stable isotopes (δ¹⁸O and δ²H) differentiated four water types: saline springs, freshwater spring, fresh groundwater, and saline groundwater. The results indicate that meteoric water is the main origin of these water resources. Halite dissolution from the salt dome was identified as the origin of salinity. The Na/Cl and Cl/Br ratios confirmed the results. Groundwater compositions in the southwestern part of the area are affected by the intrusion of saltwater from the salt dome. The average saltwater fraction in the some water wells is about 0.2%. In the south and southwestern part of the area, the saltwater fraction is positive in mixed freshwater/saltwater (Group 2). Different processes interact together to change the hydrochemical properties of Fasa’s alluvial aquifer. The main processes that occur in the aquifer are mixing, gypsum dissolution, and calcite precipitation.     

Identification and evaluation of the hydrogeochemical processes of the lower part of Wadi Siham catchment area, Tihama plain, Yemen

One hundred forty-eight groundwater samples were collected from the lower part of Wadi Siham catchment area for hydrogeochemical investigations to understand the hydrogeochemical processes affecting groundwater chemistry and their relation with groundwater quality. Groundwater in the study area is abstracted from different aquifers. The study area is characterized by arid climate and extremely high relative humidity. The results indicate that groundwater in the study area is fresh to brackish in nature. The abundance of the major ions is as follows: Na⁺¹?>?Ca⁺²?>?Mg⁺²?≥?K⁺¹ and Cl^?1?>?HCO ₃ ^?1 ?>?SO ₄ ^?2 ?>?NO ₃ ^?1 . Various graphical and ionic ration plots, statistical analyses, and saturation indices calculations have been carried out using chemical data to deduce a hydrochemical evaluation of the study area. The prevailing hydrogeochemical processes operating in the study area are dissolution, mixing, evaporation, ion exchange, and weathering of silicate minerals in the eastern part (recharge areas). The reverse ion exchange and seawater intrusion control the groundwater chemistry along the Red Sea coast areas and few parts of the study area. Deterioration in groundwater quality from anthropogenic activities has resulted from saltwater intrusion along the coastal areas due to groundwater overpumping and extensive use of fertilizers and infiltration of sewage water. Salinity and nitrate contamination are the two major problems in the area, which is alarming considering the use of this water for drinking.     

基于多元统计分析的地下水水源地污染识别

为实现地下水水源地的科学保护,识别水源地可能的污染源,通过采集吴忠市金积水源地保护区及周边16个水井地下水样品,依据采样测试分析结果,遵循连续性和代表性原则,选择了电导率、溶解性总固体、总硬度、浊度、溶解氧、氟化物、亚硝酸盐和细菌总数等8个指标进行多元统计分析。采用因子分析法,提取出4个公因子,利用因子得分进行多元线性回归,实现对金积水源地可能的地下水污染源的识别。结果表明,因子分析提取出的4个公因子,解释了所选样本总方差的96.979%,其中第一公因子代表蒸发浓缩作用,第二公因子代表粪便污染,第三公因子代表含氟矿物的溶解和工业污染,第四公因子代表自然作用,且各污染因子对不同采样点的污染程度不同,四个公因子对地下水水质的贡献率分别为:42.63%,29.23%,22.40%和5.74%。     

Recharge sources and hydrogeochemical evolution of groundwater in the coal-mining district of Jiaozuo, China

Investigations in the Jiaozuo coal-mining district (China) aim to link water-inrush aquifers with the sources of groundwater recharge. Concentrations of TDS, HCO ₃ ^– , Cl^– and Na⁺ in the groundwater samples gradually decrease with increasing depth; in contrast, the factor 1 value of the Q-mode analysis gradually increases, which indicates that the deep groundwater may upflow, recharging the aquifers near the faulted zone. Some groundwater samples (above the local meteoric water line and ‘evaporation line 1’) may originate from recharge by infiltrating local rainfall. Spring and river samples are symmetrically distributed on the regression line of the Ordovician and Carboniferous limestone aquifer groundwater (δ²H?=?3.76?×?δ¹⁸O?–?31.77) and may, therefore, originate from groundwater recharge in the northern Taihang mountains. This mechanism is supported by the observation that groundwater levels change with rainfall. According to radiocarbon residence-time estimates, two groundwater sample sites may have been recharged during the late glacial stage.     

Nitrate pollution of groundwater in Toyserkan,western Iran

A total of 95 groundwater samples were collected from Toyserkan, western Iran to assess the chemical composition and nitrate (NO₃ ⁻) status of groundwater. The most prevalent water type is Ca–HCO₃ followed by water types Ca–Mg–HCO₃. In comparison with the World Health Organization (WHO) drinking water guideline of 50 mg l⁻¹ for NO₃ ⁻, a total of nine wells (9.5%) showed higher concentrations. In 36% of samples (34) NO₃ ⁻ concentration was low (<20 mg l⁻¹), and in 53.7% of samples (51), in the range of 20–50 mg l⁻¹. The samples were classified into four groups based on NO₃ ⁻ and chloride (Cl⁻) concentrations. Of the samples, 40% were classified as group 4 and were relatively high in Cl⁻ and NO₃ ⁻ (Cl⁻ > 47 mg l⁻¹, NO₃ ⁻ > 27 mg l⁻¹). The high correlation between NO₃ ⁻ and Cl⁻ (r = 0.86, p < 0.01) is consistent with a manure source, resulting from the practice of adding salt to animal feed. Pollution of groundwaters appeared to be affected by the application of inorganic fertilizer at greater than agronomic rates, Cl-salt inputs, and irrigation practice.     

Assessment of groundwater quality and hydrochemical characteristics in Farashband plain,Iran

Groundwater in Farashband plain, Southern Iran, is the main source of water for domestic and agricultural uses. This study was carried out to assess the overall water quality and identify major variables affecting the groundwater quality in Farashband plain. The hydrochemical study was undertaken by randomly collecting 84 groundwater samples from observation wells located in 13 different stations covering the entire plain in order to assess the quality of the groundwater through analysis of major ions. The water samples were analyzed for various physicochemical attributes. Groundwater is slightly alkaline and largely varies in chemical composition; e.g., electrical conductivity (EC) ranges from 2314 to 12,678 μS/cm. All the samples have total dissolved solid values above the desirable limit and belong to a very hard type. The abundance of the major ions is as follows: Na⁺ > Ca²⁺ > Ma²⁺ > K⁺ and Cl^? > SO₄ ^2– > HCO₃ ^?. Interpretation of analytical data shows three major hydrochemical facies (Ca–Cl, Na–Cl, and mixed Ca–Mg–Cl) in the study area. Salinity, total dissolved solids, total hardness, and sodium percentage (Na%) indicate that most of the groundwater samples are not suitable for irrigation as well as for domestic purposes and far from drinking water standard. A comparison of groundwater quality in relation to drinking water standards showed that most of the water samples are not suitable for drinking purposes. Based on the US salinity diagram, most of samples belong to high salinity and low to very high sodium type.     

Distribution of fluoride in groundwater of Maku area, northwest of Iran

High fluoride groundwater occurs in Maku area, in the north of West Azarbaijan province, northwest of Iran. Groundwater is the main source of drinking water for the area residents. Groundwater samples were collected from 72 selected points including 40 basaltic and 32 nonbasaltic springs and wells, in two stages, during June and August 2006. The areas with high fluoride concentrations have been identified, and the possible causes for its variation have been investigated. Regional hydrogeochemical investigation indicates that water-rock interaction is probably the main reason for the high concentration of ions in groundwater. The concentration of F⁻ in groundwater is positively correlated with that of HCO₃ ⁻ and Na⁺, indicating that groundwater with high HCO₃ ⁻ and Na⁺ concentrations help to dissolve some fluoride-rich minerals. All of the water samples, collected from the basaltic areas do not meet the water quality standards for fluoride concentration and some other parameters. Hence, it is not suitable for consumption without any prior treatment. Inhabitants of the area that obtain their drinking water supplies from basaltic springs and wells are suffering from dental fluorosis. The population of the study area is at a high risk due to excessive fluoride intake especially when they are unaware of the amount of fluoride being ingested due to lack of awareness.     

Identification and evolution of hydrogeochemical processes in the groundwater environment in an area of the Palar and Cheyyar River Basins,Southern India

The Palar and Cheyyar River Basins in Tamil Nadu state of Southern India are characterised by different geological formations, and groundwater is the major source for domestic, agricultural and other water-related activities. Hydrogeochemical studies were carried out in this area with the objective of identifying the geochemical processes and their relation to groundwater quality. Groundwater samples were collected once a month from 43 groundwater wells in this area from January 1998 to July 1999. Sampling procedures and chemical analysis were carried out as per the standard methods. Chemical data are used for mathematical calculations and graphical plots to understand the chemical process and its relation to the groundwater quality. The chemical composition of groundwater in the central part of the study area mainly depends on the recharge from lakes and the river, which is explained by a mixing mechanism. In addition, weathering of silicate minerals controls the concentration of major ions such as sodium, calcium, magnesium and potassium in the groundwater of this area. Further, the activity ratios indicate that the groundwater is in equilibrium with kaolinite, smectite and montmorrillonite. The reverse ion exchange process controls the concentration of calcium, magnesium and sodium in hard rock formations, and dissolution of carbonate minerals and accessory minerals is the source of Ca and Mg, in addition to cation exchange in the sedimentary formations. In general, the chemical composition of the groundwater in this area is influenced by rock–water interaction, dissolution and deposition of carbonate and silicate minerals, ion exchange, and surface water interactions.     

Evaluation of hydrogeochemical processes and groundwater quality in the Jhansi district of Bundelkhand region, India

A base line study involving analysis of groundwater samples from the Jhansi district were carried out to determine the major and trace element chemistry and to assess the hydrogeochemical processes and water quality for domestic and irrigation uses. Study results show that groundwater is mildly acidic to alkaline in nature and HCO₃ ^?, Cl^?, Ca²⁺, Na⁺ and Mg²⁺ are the major contributing ions for the dissolved loads. The data plotted on the Gibbs and Piper diagrams reveal that the groundwater chemistry is mainly controlled by rock weathering with secondary contribution from anthropogenic sources. In a majority of the groundwater samples, alkaline earth metals exceed alkalies and weak acid dominate over strong acids. Ca–Mg–HCO₃ is the dominant hydrogeochemical facies in the majority of the groundwater samples. The computed saturation indices demonstrate that groundwater is oversaturated with respect to dolomite and calcite. Kaolinite is the possible mineral that is in equilibrium with the water, implying that the groundwater chemistry favors kaolinite formation. A comparison of groundwater quality parameters in relation to specified limits for drinking water shows that the concentrations of TDS, F^?, NO₃ ^?, total hardness and Fe are exceeding the desirable limits in many water samples. Quality assessment for irrigation uses reveal that the groundwater is of good to suitable category. Higher salinity and residual sodium carbonate values at some sites restrict the suitability of groundwater and need an adequate drainage and water management plan for the area.     

Characterising the main karst aquifers of the Alvand basin, northwest of Zagros, Iran, by a hydrogeochemical approach

The Alvand River basin, situated in the northwest of the Zagros mountain range, Iran, drains carbonate aquifers through some important karst springs. The physical, chemical and isotopic characteristics of spring water were studied for two years in order to assess the origin of groundwater and determine the factors driving the geochemical composition. Principal components analysis was used to identify the main factors controlling the water chemistry. Two groups of springs were identified: (1) low mineralisation, ion concentration, especially sulphate, low temperature, light isotope composition and high elevation of the recharge area, and (2) moderate to high mineralisation, especially sulphate, higher temperature, heavy isotope composition and low altitude of the recharge area. The main factors controlling the groundwater composition and its seasonal variations are the geology, because of the presence of evaporite formations, the elevation and the rate of karst development. In both groups, the carbonate chemistry is diagnostic of the effect of karst development. The supersaturation with respect to calcite indicates CO₂ degassing, occurring either inside the aquifer in open conduits, or at the outlet in reservoirs. The undersaturation with respect to calcite shows the existence of fast flow and short residence-time conditions inside the aquifer. A PCA analysis showed that, contrary to most developed karst systems, where dilution occurs during the wet season, leaching of the gypsum-bearing Gachsaran Formation by rainwater produced higher mineralisation.

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Resumen La cuenca del río Alvand, situada en el noreste de la cadena montañosa Zagros drena acuíferos compuestos por carbonatos a través de manantiales kársticos. Durante dos años se estudiaron las características físicas, químicas e isotópicas del agua de manantial con el objetivo de determinar el origen del agua subterránea y de los factores que controlan su composición geoquímica. Se utililizó el análisis de componentes principales para identificar los factores principales que controlan la química del agua. Se identificaron dos grupos de mantaniales: (1) de baja mineralización, concentración de iones especialmente sulfatos, y baja temperatura, composición de isotopos livianos y elevación alta del área de recarga, y (2) mineralización moderada y alta, especialmente, sulfatos, y temperatura más alta, composición de isotopos pesados y altitud más baja del agua de recarga. Los factores principales que controlan la composición del agua subterránea y sus variaciones estacionales son la geología debido a la presencia de formaciones evaporitas, la elevación y la tasa a la que se desarrolla el karst. En ambos grupos la química de los carbonatos es un diagnóstico del efecto del desarollo de la estructura kárstica. La supersaturación con respecto a la calcita indica presencia de CO₂ que está en proceso de degasificación que ocurre dentro de acuífero en conductos abiertos o a la salida en reservorios. La subsaturación en lo referente a la calcita muestra la existencia de flujo rápido y de tiempos cortos de residencia al interior del acuífero. El análisis de componentes principales muestra que a diferencia de la mayor parte de sistemas kársticos en donde la dilución ocurre durante la temporada de lluvias, la lixiviación de la formación Gachsaran que contiene yeso a causa de lluvia produce mineralizaciones más altas.

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Résumé Le bassin de la rivière Alvand, situé dans le nord-ouest de la chaîne de montagne Zagros, draine des aquifères carbonatés par le biais dun important réseau de sources karstiques. Les caractéristiques physiques, chimiques et isotopiques de leau provenant des sources ont été étudiées pendant deux ans afin de déterminer lorigine de leau souterraine et les facteurs responsables de sa composition chimique actuelle. Lanalyse des éléments chimiques majeurs a été utilisée pour identifier les processus qui contrôlent la composition chimique de leau. Deux groupes différents de sources ont été identifiés: (1) faible minéralisation et concentration en ions, spécialement en sulfates, faible température, composition isotopique légère et haute élévation de la zone de recharge, et (2) minéralisation moyenne à élevée, particulièrement en sulfates, température élevée, composition isotopique lourde et plus basse altitude de la zone de recharge. Les facteurs principaux qui contrôlent la composition et la variation saisonnière de leau souterraine sont la géologie, en raison de la présence dévaporites, lélévation et le taux de développement des karsts. Dans les deux groupes, la teneur en carbonates est un diagnostic de leffet du développement de la structure des karsts. La sursaturation par rapport à la calcite indique un dégazage en CO₂ qui a lieu soit à lintérieur de laquifère, dans les conduits ouverts, ou à sa sortie, dans les réservoirs. La sous-saturation par rapport à la calcite indique lexistence dun écoulement rapide et un faible temps de résidence dans laquifère. Une analyse des éléments chimiques majeurs a démontré que contrairement aux systèmes de karst les mieux développés où la dilution a lieu lors de la saison humide, le lessivage du gypse de la formation de Gachsaran par leau de pluie produit une minéralisation plus élevée.