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

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

Integrated hydrochemical assessment of the Quaternary alluvial aquifer of the Guadalquivir River, southern Spain

The alluvial aquifer of the Guadalquivir River comprises shallow Quaternary deposits located in the central-eastern part of the Province of Jaén in southern Spain, where groundwater resources are used mainly for crop irrigation in an important agricultural area. In order to establish the baseline hydrochemical conditions and processes determining the groundwater quality, groundwater and river water samples were collected as part of an integrated investigation that coupled multivariate statistical analysis with hydrochemical methods to identify and interpret the groundwater chemistry of the aquifer system. Three main hydrochemical types (Mg–Ca–HCO₃, Ca–Mg–SO₄–HCO₃–Cl and Na–Ca–Mg–Cl–SO₄) were identified. Further interpretation, using R-mode principal components analysis (PCA) conducted with 13 hydrochemical variables, identified two principal components which explain ⅔ of the variance in the original data. In combination with the hydrochemical interpretation, mineralogical analyses of the aquifer sediment together with inverse geochemical modelling using NETPATH showed that dedolomitization (calcite precipitation and dolomite dissolution driven by gypsum dissolution) is the principal hydrochemical process controlling the regional groundwater chemistry. Other processes such as silicate weathering, ion exchange, mixing between river water and groundwater, and agricultural practices also affect the groundwater chemistry.     

A geochemical study of the impact of irrigation and aquifer lithology on groundwater in the Upper Yakima River Basin,Washington, USA

The Yakima River, a major tributary of the Columbia River, is currently overallocated in its surface water usage in part because of large agricultural water use. As a result, groundwater availability and surface water/groundwater interactions have become an important issue in this area. In several sub-basins, the Yakima River water is diverted and applied liberally to fields in the summer creating artificial recharge of shallow groundwater. Major ion, trace element, and stable isotope geochemistry of samples from 26 groundwater wells from a transect across the Yakima River and 24 surface waters in the Kittitas sub-basin were used to delineate waters with similar geochemical signatures and to identify surface water influence on groundwater. Major ion chemistry and stable isotope signatures combined with principal component analysis revealed four major hydrochemical groups. One of these groups, collected from shallow wells within the sedimentary basin fill, displays temporal variations in NO₃ and SO₄ along with high δ¹⁸O and δD values, indicating significant contribution from Yakima River and/or irrigation water. Two other major hydrochemical groups reflect interaction with the main aquifer lithologies in the basin: the Columbia River basalts (high-Na groundwaters), and the volcaniclastic rocks of the Ellensburg Formation (Ca–Mg–HCO₃ type waters). The fourth major group has interacted with the volcaniclastic rocks and is influenced to a lesser degree by surface waters. The geochemical groupings constrain a conceptual model for groundwater flow that includes movement of water between underlying Columbia River basalt and deeper sedimentary basin fill and seasonal input of irrigation water.     

Modeling the impact of groundwater depletion on the hydrochemical characteristic of groundwater within Mullusi carbonate aquifer-west Iraq

The study of groundwater impact on the hydrochemical characteristic of groundwater within Mullusi aquifer, west Iraq was conducted using the chemical analysis results in 14 production wells and groundwater levels observation in 17 water wells. The interpretation of hydrochemical phenomena related to ions sources was determined based on spatial analysis maps of various hydrochemical ratios using ArcGis software. The study also determined the relation of groundwater velocity and static water levels with the hydrochemical ratios using statistical application of Curve expert v1.3 program. The variations of ion concentration were examined using the statistical significant differences for chemical constituents of water within Mullusi aquifer. The impact of dewatering due to high exploitation was explained by increasing the magnesium and chloride concentrations and lowering static water levels. Magnesium and chloride concentration may reach their maximum limits for drinking at a groundwater level of 485 m asl. Accordingly, any decline in the water level of Mullusi aquifer that occurs from 4.5 to 30.5 m may cause deterioration in groundwater quality. This study modeled the effect of groundwater depletion on the groundwater quality in a theoretical equations approach.     

Evaluation of the processes affecting vertical water chemistry in an alluvial aquifer of Mankyeong Watershed, Korea, using multivariate statistical analyses

Vertical variations of redox chemistry and groundwater quality were investigated in an alluvial aquifer beneath an agricultural area, in which deep groundwaters are free of NO₃, Fe, and Mn problems that are frequently encountered during the development of alluvial groundwaters. This study was performed to identify and evaluate vertical chemical processes attenuating these chemical species in the study area. For this study, the processes affecting groundwater chemistry were identified by factor analysis (FA) and the groundwater samples collected from six multilevel samplers were hierarchically classified into three different redox zones by cluster analysis (CA) based on the similarity of geochemical features. FA results indicated three major factors affecting the overall water chemistry: agricultural activities (factor 1), redox reactions (factor 2), and remnant seawater (factor 3). The groundwater quality in the study area was revealed to be controlled by a series of different redox reactions, resulting in different redox zones as a function of depth. It was also revealed that the low Fe and Mn levels in the groundwater of the deeper part are associated with sulfate reduction, which led to precipitation of Fe as iron sulfide and adsorption of Mn on it.     

Impact of agricultural activity and lithology on groundwater quality in the Merdja area, Tebessa, Algeria

This work presents results of the hydrogeological and hydrochemical studies on groundwater samples from the alluvial aquifer of Merdja in Tébessa, located in the Western part of this town. Its groundwater resources are used mainly for crop irrigation in an agriculture dominated area. Hydrochemical and water quality data obtained through a sampling period (December 2008) and analysis program indicate that nitrate pollution can be a serious problem affecting groundwater due to the use of nitrogen (N) fertilizers in agriculture. The concentration of nitrate in groundwater ranged from 19 to 281 mg/l. Considerable seasonal fluctuations in groundwater quality were observed as a consequence of agricultural practices and other factors such as annual rainfall distribution and the wadi El Kebir flow regime. The chemical composition of the water is not only influenced by agricultural practices, but also by interaction with the alluvial sediments. The dissolution of evaporites accounts for part of the Na⁺, K⁺, Cl^?, SO ₄ ^2? , Mg²⁺, and Ca²⁺, but other processes, such as calcite precipitation and dedolomitization, also contribute to groundwater chemistry.     

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.     

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 of hydrogeochemical zones in postglacial buried valley aquifer (Wielkopolska Buried Valley aquifer,Poland)

This article presents the difficulty in identifying the hydrochemical zoning of a semi-confined aquifer, characterised by a relative small spatial differentiation of groundwater chemistry. It is shown that multivariate statistical methods can be used for the recognition and interpretation of the groundwater chemistry distribution in an aquifer. The hydrochemical zonation caused by both natural and anthropogenic processes was identified using factor analyses in combination with a classical interpretation of the hydrogeological material. The interpretation of the groundwater chemistry allows both identification of the aquifer recharge mechanism and verification of the groundwater-flow system.     

Groundwater geochemistry of a small reservoir catchment in Central Tunisia

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

The geochemical and isotopic composition of aquifer systems in the deltaic region of the Po River plain (northern Italy)

The chemical and hydrodynamic characteristics of groundwater in deltaic regions are strongly influenced by the complex stratigraphy of these areas, caused by the continuously varying depositional environments associated with their recent hydrographic evolution. As a case study, the eastern sector of the Po River plain, northern Italy, has been investigated to understand the quality of the available groundwater resources. Based on the analysis of hydrochemical and isotopic data, the recharge characteristics, the groundwater residence time and the aquifer vulnerability are defined. The results show significant qualitative degradation of the unconfined aquifer due to the shallow depth to water, while in the underlying confined aquifer, a hydrochemical facies of Ca–HCO₃ type prevails. The spatial variation and relationship between oxygen-18 and deuterium determine: firstly, hydraulic separation of the two hydrogeological units; secondly, direct infiltration of local precipitation to the unconfined aquifer; thirdly, the occurrence of waters originating in the Alps and locally from the Apennines, pervading the confined aquifer. The tritium results suggest local mixing between the superficial waters and the confined aquifer, occurring along the palaeo-river channels. This increases the pollution vulnerability of the confined hydrogeological unit within the plain, which is the only natural groundwater resource exploited for water supply.     

Application of numerical modeling for groundwater flow and contaminant transport analysis in the basaltic terrain, Bagalkot, India

A three-dimensional steady-state finite difference groundwater flow model is used to quantify the groundwater fluxes and analyze the subsurface hydrodynamics in the basaltic terrain by giving particular emphasis to the well field that supplies domestic, agricultural, and industrial needs. The alluvial aquifer of the Ghatprabha River comprises shallow tertiary sediment deposits underlain by peninsular gneissic complex of Archean age, located in the central–eastern part of the Karnataka in southern India. Integrated hydrochemical, geophysical, and hydrogeological investigations have been helped in the conceptualization of groundwater flow model. Hydrochemical study has revealed that groundwater chemistry mainly controlled by silicate weathering in the study area. Higher concentration of TDS and NO₃-N are observed, due to domestic, agriculture, and local anthropogenic activities are directed into the groundwater, which would have increased the concentration of the ions in the water. Groundwater flow model is calibrated using head observations from 23 wells. The calibrated model is used to forecast groundwater flow pattern, and anthropogenic contamination migration under different scenarios. The result indicates that the groundwater flows regionally towards the south of catchment area and the migration of contamination would be reached in the nearby well field in less than 10 years time. The findings of these studies are of strong relevance to addressing the groundwater pollution due to indiscriminate disposal practices of hazardous waste in areas located within the phreatic aquifer. This study has laid the foundation for developing detailed predictive groundwater model, which can be readily used for groundwater management practices.     

Impact of agricultural activity and geologic controls on groundwater quality of the alluvial aquifer of the Guadalquivir River (province of Jaén,Spain): a case study

The alluvial aquifer of the Alto Guadalquivir River is one of the most important shallow aquifers in Jaén, Spain. It is located in the central-eastern part of the province, and its groundwater resources are used mainly for crop irrigation in an agriculture-dominated area. Hydrochemical and water-quality data obtained through a 2-year sampling (2004–2006) and analysis program indicate that nitrate pollution is a serious problem affecting groundwater due to the use of nitrogen (N)-fertilizers in agriculture. During the study, 231 water samples were collected from wells and springs to determine water chemistry and the extent of nitrate pollution. The concentration of nitrate in groundwater ranged from 1.25 to 320.88 mg/l. Considerable seasonal fluctuations in groundwater quality were observed as a consequence of agricultural practices and other factors such as annual rainfall distribution and the Guadalquivir River flow regime. The chemical composition of the water is not only influenced by agricultural practices, but also by interaction with the alluvial sediments. The dissolution of evaporites accounts for part of the Na⁺, K⁺, Cl⁻, SO₄ ²⁻, Mg²⁺, and Ca²⁺, but other processes, such as calcite precipitation and dedolomitization, also contribute to groundwater chemistry.     

Processes Controlling Groundwater Chemistry from Mulakalacheruvu Area,Chittoor District,Andhra Pradesh,South India: A Statistical Approach Based on Hydrochemistry

In India groundwater is an important source for domestic and agricultural purposes. Management of this resource is very important to meet the increasing demand of water. In this study, the ionic concentrations of groundwater from Mulakalacheruvu area, Chittoor district, Andhra Pradesh, South India have been calculated during May 2014 and the major ionic concentrations have been analyzed by hydrochemcial and statistical methods in order to trace the main processes controlling the groundwater chemistry. The results have suggested that these groundwater samples belong to Na-HCO₃ (18 samples), Ca-HCO₃ (16 samples) and Mg-HCO₃ (6 samples) types. The hydrochemical methods suggest that the rocks in the aquifer system are sources of the major ions in the groundwater, and the silicate is the main mineral phase. Three sources viz. mafic silicate, felsic silicates and easily soluble minerals have been identified as responsible for the chemical variations of the groundwater. Further, the source contributions of silicate minerals for the groundwater hydrochemistry have been analyzed. These results suggest that the hydrochemistry of the groundwater in the south-eastern area is mainly controlled by weathering of felsic silicate (61-100%), whereas the north-western area is principally contributed by mafic silicate minerals (48-100%).     

Redox zonation for different groundwater flow paths during bank filtration: a case study at Liao River,Shenyang, northeastern China

The spatial and temporal distribution of redox zones in an aquifer is important when designing groundwater supply systems. Redox zonation can have direct or indirect control of the biological and chemical reactions and mobility of pollutants. In this study, redox conditions are characterized by interpreting the hydrogeological conditions and water chemistry in groundwater during bank infiltration at a site in Shenyang, northeast China. The relevant redox processes and zonal differences in a shallow flow path and deeper flow path at the field scale were revealed by monitoring the redox parameters and chemistry of groundwater near the Liao River. The results show obvious horizontal and vertical components of redox zones during bank filtration. Variations in the horizontal extent of the redox zone were controlled by the different permeabilities of the riverbed sediments and aquifer with depth. Horizontally, the redox zone was situated within 17 m of the riverbank for the shallow flow path and within 200 m for the deep flow path. The vertical extent of the redox zone was affected by precipitation and seasonal river floods and extended to 10 m below the surface. During bank filtration, iron and manganese oxides or hydroxides were reductively dissolved, and arsenic that was adsorbed onto the medium surface or coprecipitated is released into the groundwater. This leads to increased arsenic content in groundwater, which poses a serious threat to water supply security.     

Hydrogeochemistry and isotope techniques to determine water interactions in groundwater-dependent shallow lakes,Wet Pampa Plain,Argentina

This paper gives an account of the implementation of hydrochemical and isotopic techniques to identify and explain the processes that govern solute exchange in two groundwater-dependent shallow lakes in the Southeastern Pampa Plain of Argentina. Water samples (lakes, streams, spring water and groundwater) for hydrochemical and stable isotopic determination were collected and the main physical–chemical parameters were measured. The combination of stable isotope data with hydrogeochemical techniques was used for the identification of sources and preferential recharge areas to these aquatic ecosystems which allowed the explanation of the lake water origin. The hydrochemical processes which explain Los Padres Lake water chemistry are evaporation from groundwater, CO₂ input, calcite dissolution, Na⁺ release by Ca²⁺ and Mg²⁺ exchange, and sulfate reduction. The model that best aligns with La Brava Lake hydrochemical constraints includes: mixing, CO₂ and calcite dissolution, cationic exchange with Na⁺ release and Mg²⁺ adsorption, and to a lesser extent, Ca/Na exchange. This model suggests that the fractured aquifer contribution to this water body is greater than 50 %. An isotopic-specific fingerprint for each lake was identified, finding a higher evaporation rate for La Brava Lake compared to Los Padres Lake. Isotopic data demonstrate the importance of these shallow lakes as recharge areas to the regional aquifer, becoming areas of high groundwater vulnerability. The Tandilia Range System, considered in many hydrogeological studies as the impermeable bedrock of the Pampean aquifer, acts as a fissured aquifer in this area, contributing to low salinity waters and with a fingerprint similar to groundwater isotopic composition.     

The hydrochemical characteristics and evolution of groundwater and surface water in the western part of the River Nile, El Minia district, Upper Egypt

A combination of major and trace elements have been used to characterize surface- and groundwater in El Minia district, Egypt. Surface water versus groundwater chemistry data enabled geographical zonation and chemical types to be differentiated. The main target of this research is to investigate the groundwater quality and hydrochemical evaluation. The situation is further complicated by contamination with lithogenic and anthropogenic (agricultural and sewage wastewaters) sources and low plan exploitation techniques. The investigated Pleistocene aquifer is composed of sand and gravel of different sizes, with some clay intercalation. The semi-confined condition was around the River Nile shifted to unconfine outside the floodplain. The groundwater flow generally from south to north and locally diverts towards the western part from the River Nile. Fifty-six, 11, five, and two water samples were collected from the Pleistocene aquifer, River Nile, Ibrahimia canal, and Al Moheet drain, respectively. The collected water samples were analyzed for major and trace elements. The toxic metal concentrations of Al Moheet drain are higher than those in the River Nile and the Ibrahimia canal. Cr, Hg, As, and Cd concentrations in the River Nile and Ibrahimia canal are fluctuated above and below the WHO drinking standards. Se concentration in River Nile and Ibrahimia canal is below WHO drinking and irrigation guidelines. Total dissolved solid content in groundwater is generally low, but it is increased due to the western part of the study area. The geographic position of the River Nile, Ibrahimia canal, and Al Moheet drain impact on the groundwater quality. The PHREEQC confirm the high mixing proportions from the River Nile into the groundwater and decline away from it. In addition to the thicknesses of the Pleistocene, aquifer and aquitard layer enhance the River Nile and agricultural wastewaters intrusion into the aquifer system. The toxic metal concentrations (Pb, Cd, Cr, PO₄, Se, Mn, As, Hg, Ni, Al, Fe, and SIO₂) in groundwater were increased mainly in the northwestern and southeastern part (far from the River Nile). It is attributed to anthropogenic, high vulnerability rate (unconfined), and partially to lithogenic. In most localities, the groundwater are unsuitable for drinking and irrigation purposes with respect to Se concentration, while they are unsuitable for dinking according Mn, As, and Hg contents. There are some Cd and Pb anomalies concentrations, which cause severe restriction if used in irrigation. The results suggested that significant changes are urgently needed in water use strategy to achieve sustainable development.     

Modeling freshening time and hydrochemical evolution of groundwater in coastal aquifers of Shenzhen,China

This work investigated the freshening time and hydrochemical evolution of coastal groundwater in two brackish aquifers in Shenzhen, China. One was the brackish aquifer that resulted from heavy pumping, and the other was the aquifer reclaimed from the coastal sea. Freshening time and hydrochemical evolution of brackish aquifers were quantitatively evaluated using PHREEQC 2.0, a one-dimensional reactive-transport model. Freshening time was shown to mainly depend on pore water velocity, while the chemical composition of groundwater was determined by the cation exchange capacity of the aquifer. It was shown that after heavy pumping ceased, the freshening time for the original coastal aquifer ranged from 20 to over 80 years. While for the coastal reclaimed aquifer, the freshening time was from 85 to 140 years, which depended on the hydraulic conductivity of the fill materials in the reclaimed site. During aquifer freshening, groundwater evolved from Na–Cl type to Ca–Mg–HCO₃ or Na–HCO₃ type. A sensitivity analysis showed that the freshening time was most sensitive to the pore water velocity in the aquifer, while the groundwater chemical composition was most sensitive to the values of cation exchange capacity of the aquifer. As for the dispersivity, it had almost no effect on the freshening time and the chemical composition of groundwater.     

Spatial distribution of groundwater quality parameters in the Velika Morava River Basin,central Serbia

The reported study includes analysis of 14 physico-chemical parameters of alluvial groundwater based on data collected from 26 piezometers in the Velika Morava River Basin from 2004 to 2014. Eleven of the parameters were assessed applying hierarchical cluster analysis and principal component analysis to examine the spatial distribution, identify the main processes in groundwater variations and segregate the dominant sampling sites based on the characteristic parameters. A Piper diagram shows that the studied alluvial groundwaters are predominantly of the Ca²⁺–HCO₃^? type (67.3%) and to a lesser extent of the mixed Ca²⁺–Mg²⁺–HCO₃^? type (21.6%). Hierarchical clustering results in four clusters depending on the similarities of the hydrochemical parameters. Principal component analysis explains 65.4% of total variance with PC1 (32.5% variance), PC2 (19.8% variance) and PC3 (13.1% variance). A comparative analysis reveals that the main processes responsible for the hydrochemical composition of groundwater in the Velika Morava alluvion are carbonate dissolution-anthropogenic pressure, feldspar weathering and migration caused by river–aquifer interaction. Considerable loading of the alluvial groundwater caused by a complex geologic framework, natural factors and human activities in the river basin contributed to the segregation of six dominant sampling sites. The obtained results can be very useful in the development of an optimal spatial plan for groundwater monitoring, focusing on increasing the density of the national monitoring network and frequency of assessing alluvial groundwater on the dominant sampling sites (from annual to seasonal).     

Recharge source and hydrogeochemical evolution of shallow groundwater in a complex alluvial fan system,southwest of North China Plain

Many cities around the world are developed at alluvial fans. With economic and industrial development and increase in population, quality and quantity of groundwater are often damaged by over-exploitation in these areas. In order to realistically assess these groundwater resources and their sustainability, it is vital to understand the recharge sources and hydrogeochemical evolution of groundwater in alluvial fans. In March 2006, groundwater and surface water were sampled for major element analysis and stable isotope (oxygen-18 and deuterium) compositions in Xinxiang, which is located at a complex alluvial fan system composed of a mountainous area, Taihang Mt. alluvial fan and Yellow River alluvial fan. In the Taihang mountainous area, the groundwater was recharged by precipitation and was characterized by Ca–HCO₃ type water with depleted δ¹⁸O and δD (mean value of −8.8‰ δ¹⁸O). Along the flow path from the mountainous area to Taihang Mt. alluvial fan, the groundwater became geochemically complex (Ca–Na–Mg–HCO₃–Cl–SO₄ type), and heavier δ¹⁸O and δD were observed (around −8‰ δ¹⁸O). Before the surface water with mean δ¹⁸O of −8.7‰ recharged to groundwater, it underwent isotopic enrichment in Taihang Mt. alluvial fan. Chemical mixture and ion exchange are expected to be responsible for the chemical evolution of groundwater in Yellow River alluvial fan. Transferred water from the Yellow River is the main source of the groundwater in the Yellow River alluvial fan in the south of the study area, and stable isotopic compositions of the groundwater (mean value of −8.8‰ δ¹⁸O) were similar to those of transferred water (−8.9‰), increasing from the southern boundary of the study area to the distal end of the fan. The groundwater underwent chemical evolution from Ca–HCO₃, Na–HCO₃, to Na–SO₄. A conceptual model, integrating stiff diagrams, is used to describe the spatial variation of recharge sources, chemical evolution, and groundwater flow paths in the complex alluvial fan aquifer system.