Major ion chemistry of groundwater in a river basin: a study from India

Groundwater is the prime source in the area of Varaha River Basin, Andhra Pradesh, India. Groundwater samples collected during pre- and post-monsoon were analyzed for major ion chemistry to understand the operating mechanism of geochemical processes for variation of groundwater quality. Low ionic concentration is observed in the groundwater occurring at topographic-highs and towards the river compared to the rest of the area. This is caused by the influence of recharge water. Geochemistry of groundwater is observed to be mainly controlled by the rock-weathering, mineral dissolution, leaching, ion exchange and evaporation, and is subsequently modified by the anthropogenic and marine activities. Contribution of residual soluble salts below the depth of 5 m from the ground surface is high, while it is low beyond the depth of 5 m. Anthropogenic activities cause an accumulation of excess residual soluble salts in the former depth and the content of this soluble matter is reduced by the clay products beyond the latter depth. Seasonal ionic concentration of groundwater is greatly influenced by the recharge process with reference to topographical features, lithological characteristics and anthropogenic activities. Groundwater quality is classified as mixed and non-carbonate alkali groups due to a combined action of geogenic/anthropogenic and marine sources, respectively. The groundwater quality is above the adequacy level for both drinking and irrigation, and appropriate management measures are recommended for sustainable development.     

Factors controlling mechanisms of groundwater salinization and hydrogeochemical processes in the Quaternary aquifer of the Eastern Nile Delta, Egypt

In this study, combining interpretations of conservative dissolved ions and environmental isotopes in water were used to investigate the main factors and mechanisms controlling groundwater salinization and hydrogeochemical processes in the Eastern Nile Delta, Egypt. Hydrogeochemical and isotopic study has been carried out for 61 water samples from the study area. Total dissolved solid (TDS) contents of groundwater are highly variable rising along flowpath from the south (410 mg/L) to the north (14,784 mg/L), implying significant deterioration and salinization of groundwater. Based on TDS and ionic ratios, groundwater samples were classified into three groups. In low-saline groups, water chemistry is greatly influenced by cation exchange, mineral dissolution/precipitation, anthropogenic pollutants and mixing with surface water. Whilst, in high-saline groups, water chemistry is affected by salt-water intrusion, reverse cation exchange and evaporation. The chemical constituents originating from saline water sources, reverse ion exchange and mineral dissolution are successfully differentiated using ionic delta and saturation index approaches. The δ¹⁸O–δ²H relationship plots on a typical evaporation line, suggesting potential evaporation of the recharging water prior to infiltration. Isotope evidence concludes that the groundwater have been considerably formed by mixing between depleted meteoric water recharged under different climatic conditions and recently infiltrating enriched surface water and excess of irrigation water. The δ¹⁸O data in conjunction with chloride concentrations provide firm evidence for impact of dissolution of marine-origin evaporite deposits, during past geologic periods, on groundwater salinity in the northern region. Moreover, the relation between ¹⁴C activities and Cl^? concentration confirms this hypothesis.     

Isotopic and geochemical characteristics of groundwater in the Senegal River delta aquifer: implication of recharge and flow regime

Groundwater and surface water samples were collected to improve understanding of the Senegal River Lower Valley and Delta system, which is prone to salinization. Inorganic ion concentrations and environmental isotopes (¹⁸O, ²H and ³H) in groundwater, river, lake and precipitation were investigated to gain insight into the functioning of the system with regard to recharge sources and process, groundwater renewability, hydraulic interconnection and geochemical evolution. The geochemical characteristics of the system display mainly cation (Ca²⁺ and/or Na⁺) bicarbonated waters, which evolve to chloride water type; this occurs during groundwater flow in the less mineralized part of the aquifer. In contrast, saline intrusion and secondary brines together with halite dissolution are likely to contaminate the groundwater to Na–Cl type. Halite, gypsum and calcite dissolution determine the major ion (Na⁺, Cl⁻, Ca²⁺, Mg²⁺, SO₄ ²⁻ and HCO₃ ⁻) chemistry, but other processes such as evaporation, salt deposition, ion exchange and reverse exchange reactions also control the groundwater chemistry. Both surface water and groundwater in the system show an evaporation effect, but high evaporated signatures in the groundwater may be due to direct evaporation from the ground, infiltration of evaporated water or enriched rainwater in this region. The stable isotopes also reveal two types of groundwater in this system, which geomorphologically are distributed in the sand dunes (depleted isotopes) and in the flood plain (enriched isotopes). Consideration of the ³H content reinforces this grouping and suggests two mechanisms of recharge: contribution of enriched surface water in recharging the flood plain groundwater and, in the sand dunes area where water table is at depth between 8 and 13 m, slow recharge process characterized the submodern to mixed water.     

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.     

Isotope hydrogeochemical models for assessing the hydrological processes in a part of the largest continental flood basalts province of India

Continental Flood Basalts (CFB) occupy one fourth of the world’s land area. Hence, it is important to discern the hydrological processes in this complex hydrogeological setup for the sustainable water resources development. A model assisted isotope, geochemical, geospatial and geophysical study was conducted to understand the monsoonal characteristics, recharge processes, renewability and geochemical evolution in one of the largest continental flood basalt provinces of India. HYSPLIT modelling and stable isotopes were used to assess the monsoonal characteristics. Rayleigh distillation model were used to understand the climatic conditions at the time of groundwater recharge. Lumped parameter models (LPM) were employed to quantify the mean transit time (MTT) of groundwater. Statistical and geochemical models were adopted to understand the geochemical evolution along the groundwater flow path. A geophysical model was used to understand the geometry of the aquifer. The back trajectory analysis confirms the isotopic finding that precipitation in this region is caused by orographic uplifting of air masses originating from the Arabian Sea. Stable isotopic data of groundwater showed its meteoric origin and two recharge processes were discerned; (i) quick and direct recharge by precipitation through fractured and weathered basalt, (ii) low infiltration through the clayey black cotton soil and subjected to evaporation prior to the recharge. Tritium data showed that the groundwater is a renewable source and have shorter transit times (from present day to <30 years). The hydrogeochemical study indicated multiple sources/processes such as: the minerals dissolution, silicate weathering, ion exchange, anthropogenic influences etc. control the chemistry of the groundwater. Based on the geo-electrical resistivity survey, the potential zones (weathered and fractured) were delineated for the groundwater development. Thus, the study highlights the usefulness of model assisted isotopic hydrogeochemical techniques for understanding the recharge and geochemical processes in a basaltic aquifer system.     

Groundwater quality assessment using integrated geochemical methods,multivariate statistical analysis,and geostatistical technique in shallow coastal aquifer of Terengganu,Malaysia

Extensive agricultural, residential, and industrial activities have increased demand for water supplies, which can lead to groundwater quality degradation. The integration of geochemical methods, multivariate statistical analysis, and geostatistical approaches were carried out on 169 groundwater samples to elucidate the regional factors and processes that influencing the geochemical composition of groundwater in coastal shallow aquifer of Terengganu, Malaysia. Hydrochemical modelling revealed that the abundance of Ca and Mg was contributed by carbonate and silicate weathering while higher HCO₃ and Cl were resulted from reverse ion exchange reaction. Therefore, the dominant hydrogeochemical facies of groundwater was Ca-Mg-HCO₃-Cl type. The influence of salinization resulting from seawater mixing to the groundwater was corroborated by Cl/HCO₃ ratio, which affected around 50.9% of the groundwater samples slightly or moderately. Spatial mapping using ordinary kriging found that the threat of sea water intrusion is more prominent in the major river confluence especially around Terengganu and Marang River in the northeast and Dungun and Kemaman River confluence in southeast of study area. Moreover, factor analyses concluded that salinization, anthropogenic activities, reverse ion exchange, weathering processes, agricultural impact, and seasonal variations were the factors that regulate 63% of the major ion chemistry in study area. Finally, these findings showed the importance of understanding the hydrochemical characteristics for effective utilization, aquifer protection, and prediction of changes to minimize the effects of salinization and reduce human pollution such as agriculture and urbanization. It is essential steps in order to safeguard the utilization of groundwater resources for future generations.     

Evaluation of hydrogeochemical characteristics of groundwater in parts of the lower Benue Trough, Nigeria

The aim of this work is to evaluate the hydrogeochemical characteristics of groundwater in parts of the lower Benue Through in Nigeria as well as to evaluate the variation in groundwater chemistry data and the suitability of the groundwater for drinking and other domestic purposes. This was based on chemical analyses of 44 water samples from existing wells and boreholes in the study area. From the statistical analysis (wide ranges, median and standard deviation), it is obvious that there are significant variations in the quality/composition of groundwater in the period of sampling. The calculated SAR, Na% and RSC values indicated that the water is of excellent to good quality and is suitable for irrigation. Na and HCO₃ are dominant with respect to the chemical composition of the groundwater. On the basis of water chemistry, hydrochemical indices and factor analysis the dominant controls or processes affecting the distribution of geochemical variables in the study area have been shown to be water/rock interaction which is mainly controlled by carbonate and silicate dissolution as well as anthropogenic influence to a lesser extent. Additional processes include cation exchange reactions and reverse ion exchange to a minor extent.     

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

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

Assessment of groundwater chemistry in a coastal region (Kunsan, Korea) having complex contaminant sources: a stoichiometric approach

Groundwater chemistry in a coastal region (Kunsan, Korea) having complex contaminant sources was investigated. Water analysis data for 197 groundwater samples collected from the uniformly distributed sixty-six wells were used. Chemical analysis results indicate that groundwaters show wide concentration ranges in major inorganic ions, reflecting complex hydrochemical processes. Due to the complexity of groundwater chemistry, the samples were classified into four groups based on Cl and NO₃ concentrations and the processes controlling water chemistry were evaluated based on the reaction stoichiometry. The results explained the importance of mineral weathering, anthropogenic activities (nitrification and oxidation of organic matters), and Cl-salt inputs (seawater, deicer, NaCl, etc.) on groundwater chemistry. It was revealed that mineral dissolution is the major process controlling the water chemistry of the low Cl and NO₃ group (Group 1). Groundwaters high in NO₃ (Groups 2 and 4) are acidic in nature, and their chemistry is largely influenced by nitrification, oxidation of organic matters and mineral dissolution. In the case of chloride rich waters (Group 3), groundwater chemistry is highly influenced by mineral weathering and seawater intrusion associated with cation-exchange reactions.     

Groundwater Recharge and Mixing in Arid and Semiarid Regions: Heihe River Basin, Northwest China

A sound understanding of groundwater recharged from various sources occurring at different time scales is crucial for water management in arid and semi-arid river basins. Groundwater recharge sources and their geochemical evolution are investigated for the Heihe River Basin(HRB) in northwest China on the basis of a comprehensive compilation of geochemical and isotopic data. Geochemical massbalance modeling indicates that mountain-block recharge accounts for a small fraction(generally less than 5%) of the shallow and deep groundwater sustaining the oasis, whereas infiltration of rivers and irrigation water contribute most of the groundwater recharge. Dedolomitization is the primary process responsible for the changes in groundwater chemical and carbon isotope compositions from the piedmont to the groundwater discharge zone, where the dedolomitization is very likely enhanced by modern agricultural activities affecting the shallow groundwater quality. Analysis of radioactive isotopes suggests that these primary recharge sources occur at two different time scales. Radiocarbon-derived groundwater age profiles indicate a recharge rate of approximately 12 mm/year, which probably occurred during 2000–7000 years B.P., corresponding to the mid-Holocene humid period. The recharge of young groundwater on the tritium-dated time scale is much higher, about 360 mm/year in the oasis region. Infiltration from irrigation canals and irrigation return flow are the primary contributors to the increased young groundwater recharge. This study suggests that groundwater chemistry in the HRB has been influenced by the complex interaction between natural and human-induced geochemical processes and that anthropogenic effects have played a more significant role in terms of both groundwater quantity and quality.     

Effect of agricultural land use on the chemistry of groundwater from basaltic aquifers, Jeju Island, South Korea

Geochemical processes were identified as controlling factors of groundwater chemistry, including chemical weathering, salinization from seawater and dry sea-salt deposition, nitrate contamination, and rainfall recharge. These geochemical processes were identified using principal component analysis of major element chemistry of groundwater from basaltic aquifers in Jeju Island, South Korea, a volcanic island with intense agricultural activities. The contribution of the geochemical processes to groundwater chemistry was quantified by a simple mass-balance approach. The geochemical effects due to seawater were considered based on Cl contributions, whereas the effects due to natural chemical weathering were based on alkalinity. Nitrogenous fertilizers, and especially the associated nitrification processes, appear to significantly affect groundwater chemistry. A strong correlation was observed between Na, Mg, Ca, SO₄ and Cl, and nitrate concentrations in groundwater. Correspondingly, the total major cations, Cl, and SO₄ in groundwater were assessed to estimate relative effect of N-fertilizer use on groundwater chemistry. Cl originates more from nitrate sources than from seawater, whereas SO₄ originates mostly from rainwater. N-fertilizer use has shown the greatest effect on groundwater chemistry, particularly when nitrate concentrations exceed 6–7 mg/L NO₃–N. Nitrate contamination significantly affects groundwater quality and 18% of groundwater samples have contamination-dominated chemistry.     

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.     

Hydrogeochemistry of the Saloum (Senegal) superficial coastal aquifer

Seawater has entered and concentrated in the Saloum hydrologic system up to 100 km upstream, contaminating both the surface water and the superficial 'Continental terminal' (CT) groundwater resources, and large proportions of cultivated lands. In the areas affected by saltwater contamination, chloride concentrations as high as 3,195 mg/l have been measured in the groundwater samples collected from wells located in the vicinity of the Saloum River, making the water inadequate for drinking water purposes. This paper presents the results of a study designed to characterise the current extent of the saline groundwater and the mechanism of saline surface water body/fresh groundwater mixing in relation to the groundwater flow trends. It also describes the groundwater chemical and isotopic composition and geochemical processes controlling the chemical patterns. Four major water types occur in the study area, namely Na-rich saline groundwater, Ca-Na-rich saline groundwater, Na-dominant fresh groundwater and Ca-dominant fresh groundwater. A hydrogeochemical zonation of the aquifer, based on the presence of different water families and on the groundwater flow, led to the identification of the main processes controlling the groundwater chemistry. Cation exchange reactions on the kaolinite clay mineral, calcite dissolution in the eastern zone where calcite minerals have been identified, reverse cation exchange reactions in the saline-contaminated band along the Saloum River and, to a lesser extent, a gypsum dissolution are the predominant processes. Results of i¹⁸O and iD analysis in 15 groundwater samples compared with the local meteoric line indicate that the groundwater has been affected by evaporation, and the groundwater is isotopically lighter as the depth of water table increases. In this study, i¹⁸O data were used in conjunction with chloride data to identify the source of high chloride. Results show a departure of the contaminated water samples from the seawater mixing line, which indicates that other processes rather than mixing between modern seawater and native groundwater alone increase the chloride concentrations.     

Chemical evolution of groundwater in the River Danube deposits in the southern part of the Pannonian Basin (Hungary)

Processes controlling the groundwater chemical composition were studied in the River Danube deposits, in the southeastern part of Hungary. PHREEQM, a combined geochemical and one-dimensional transport model and PHREEQE, NETPATH and WATEQF geochemical computer codes were used to simulate these processes. The main processes controlling water chemistry are equilibrium with calcite, undersaturation in dolomite and albite weathering in the recharge area, ion exchange along the flow path, and ion exchange and mixing with old water at the end of the flow path. Ion exchange seems to be the most important process controlling groundwater chemistry along the flowpath in the fluvial sediments studied. Isotopic data support the geochemical model. The groundwater ages, adjusted for the modeled C mass transfer range from 3300 to 20 200 a B.P. Cation exchange suggests that displacement of a former aqueous solution by the present groundwater occurred. This displacement is attributed to tectonic and paleoclimatic events at the end of the Pleistocene.     

Isotopic and geochemical identifications of groundwater salinisation processes in Salalah coastal plain,Sultanate of Oman

A detail investigation was carried out to improve the current knowledge of groundwater salinisation processes in coastal aquifers using hydrochemical and isotopic parameters. Data of major ions for 40 wells located in the Salalah plain aquifer, Sultanate of Oman, were collected during pre-monsoon 2004 and analysed. The groundwater changes along the general flow path towards the coast from fresh (EC < 1500 μS/cm), brackish (EC: 1500–3000 μS/cm) and saline (EC > 3000 μS/cm). Results of inverse modeling simulations using PHREEQC show that dissolution of halite may be the main source of Cl and Na in the study area. Ionic delta calculation indicates that the depletion of Na and K and enrichment of Ca and Mg in groundwater were probably attributed to reverse ion exchange reactions. During a sampling campaign conducted in October 2015, 11 groundwater samples were collected for Cl, Br and isotopic analysis (²H/¹⁸O). Molar Cl/Br ratios in fresh groundwater were higher than those of seawater, indicating the impact of halite dissolution on the groundwater quality. For saline groundwater, these ratios were less than those of seawater, showing the influence of anthropogenic input from agriculture on the same. Relatively depleted isotopic signature of all groundwater samples show that the monsoon precipitation is the main source of groundwater recharge in the study area.     

Characterisation of groundwater chemistry in an eastern coastal area of Cuddalore district,Tamil Nadu

The groundwater quality detoriation due to various geochemical processes like saline water intrusion, evaporation and interaction of groundwater with brines is a serious problem in coastal environments. Understanding the geochemical evolution is important for sustainable development of water resources. A detailed investigation was carried out to evaluate the geochemical processes regulating groundwater quality in Cuddalore district of Tamilnadu, India. The area is entirely underlined by sedimentary formations, which include sandstone, clay, alluvium, and small patches of laterite soils of tertiary and quaternary age. Groundwater samples were collected from the study area and analyzed for major ions. The electrical conductivity (EC) value ranged from 962 to 11,824 μS/cm, with a mean of 2802 μS/cm. The hydrogeochemical evolution of groundwater in the study area starts from Mg-HCO₃ type to Na-Cl type indicating the cation exchange reaction along with seawater intrusion. The Br/Cl ratio indicates the evaporation source for the ion. The Na/Cl ratios indicate groundwater is probably controlled by water-rock interaction, most likely by derived from the weathering of calcium-magnesium silicates. The plot of (Ca+Mg) versus HCO₃ suggests ions derived from sediment weathering. The plot of Na+K over Cl reflects silicate weathering along with precipitation. Gibbs plot indicates the dominant control of rock weathering. Factor analysis indicates dominance of salt water intrusion, cation-exchange and anthropogenic phenomenon in the study.     

Effect of saline water bodies on the hydrogeochemical evaluation of groundwater at Kalpakkam coastal site, Tamil Nadu

Geochemical signatures of groundwater in Kalpakkam plant site were used to identify the geochemistry of the unconfined coastal aquifer. Ground water samples collected from 14 borewells around the study area were studied for four different seasons viz. Summer, South-west monsoon, North-east monsoon and Post-monsoon to identify the major geochemical processes activated in the study area. Data obtained through chemical analyses of groundwater samples were used for graphical plots and geochemical calculations. Piper, Chloro alkaline indices and Chadda’s diagram were determined for geochemical classification of the groundwaters. Identified geochemical processes were verified and quantified using hydrogeochemical aqueous speciation model, PHREEQC to find out the Saturation Indices (SI) of the possible minerals of the study area. It was observed that majority of the bore well samples were under saturated with respect to minerals such as Gypsum, Aragonite and oversaturated with respect to dolomite and calcite. Parameters such as ion exchange and reverse ion exchange, saline water incursion were observed due to the presence of saline water bodies in addition to dissolution of minerals.     

Hydrogeochemical and Isotopic Study of Groundwater in a Semi-arid Region: Yeniceoba Plain (Cihanbeyli-KONYA), Central Anatolia,Turkey

Groundwater is the most important source of water supply in the Yeniceoba Plain in Central Anatolia,Turkey.An understanding of the geochemical evolution of groundwater is important for the sustainable development of water resources in this region.A hydrogeochemical investigation was conducted in the Plio-Quaternary aquifer system using stable isotopes(δ~(18)O andδD),tritium(~3H),major and minor elements(Ca,Na,K,Mg,Cl,SO_4,NO_3,HCO_3 and Br)in order to identify groundwater chemistry patterns and the processes affecting groundwater mineralization in this system.The chemical data reveal that the chemical composition of groundwater in this aquifer system is mainly controlled by rock/water interactions including dissolution of evaporitic minerals,weathering of silicates,precipitation/dissolution of carbonates,ion exchange,and evaporation.Based on the values of Cl/Br ratio(300 mg/l)in the Plio-Quaternary groundwater,dissolution of evaporitic minerals in aquifer contributes significantly to the high mineralization.The stable isotope analyses indicate that the groundwater in the system was influenced by evaporation of rainfall during infiltration.Low tritium values(generally1 tritium units)of groundwater reflect a minor contribution of recent recharge and groundwater residence times of more than three or four decades.     

Source of salinity in the groundwater of Lenjanat Plain,Isfahan, Iran

The present study aimed at identifying the salinity source in the groundwater of Lenjanat Plain. To do so, non-isotopic geochemical methods were employed: groundwater samples were collected seasonally from 33 wells widespread in the area, and physicochemical parameters as well as major and minor elements were measured in the 132 samples. The data collected from the field and laboratory measurements were interpreted through statistical and hydrogeochemical graphs, mass ratios and saturation indexes obtained from modeling. The results revealed that hydrogeochemical properties of the study aquifer were controlled by rock/water interactions including ion exchange, dissolution of evaporation deposits (halite and gypsum) and precipitation/dissolution of carbonates. Based on the values of Cl/Br ratio in Lenjanat groundwater (329–4,492), dissolution of evaporation deposits in aquifer was the main cause for groundwater salinity. Considering the Lenjanat groundwater geochemical properties, the data confirm the reported Cl/Br ratios for groundwater affected by the dissolution of evaporation deposits (Cl/Br > 300) and overlaps with the range of Cl/Br ratios for domestic sewage effluent groundwater. Selecting the best chemical components and their ratios in non-isotopic geochemical methods provides an accurate distinction between sources of groundwater salinity.