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1.
Aji-Chay River is one of the most important surface reservoirs of northwest of Iran, because it passes through Tabriz city and discharges to Urmia Lake, one of the largest permanent salty lakes in the world. The main objectives of the present study are to evaluate its overall water quality and to explore its hydrogeochemical characteristics, including the potential contamination from heavy metals and metalloids such as Co, Pb, Zn, Cd, Cu, Cr, Al and As. For this purpose, 12 water samples were collected from the main river body and its tributaries within Tabriz plain. The Piper diagram classified water samples mainly into Na–Cl and secondary into Ca–HCO3 and mixed Ca–Mg–Cl types, denoting a profound salinization effect. The cross-plots showed that natural geochemical processes including dissolution of minerals (e.g., carbonates, evaporites and silicates), as well as ion exchange, are the predominant factors that contribute to fluvial hydrogeochemistry, while anthropogenic activities (industrial and agricultural) impose supplementary effects. Cluster analysis classified samples into two distinct clusters; samples of cluster B appear to have elevated electrical conductivity (EC) values and trace metals concentrations such as Co, Pb and Cd, while SiO2 and Zn are low in comparison with the samples of the cluster A. The main processes controlling Aji-Chay River hydrogeochemistry and water quality were identified to be salinization and rock weathering. Both are related with geogenic sources which enrich river system with elevated values of Na+, Cl?, Ca2+, Mg2+, K+, SO4 2? and EC as a direct effect of evaporites leaching and elevated values of Pb and Cd as an impact from the weathering process of volcanic formations. According to the US salinity diagram, all of the water samples are unsuitable for irrigation as having moderate to bad quality.  相似文献   

2.
The present study investigates the hydrogeochemistry and contamination of Varamin deep aquifer located in the southeast of Tehran province, Iran. The study also evaluates groundwater suitability for irrigation uses. The hydrogeochemical study was conducted by collecting and analyzing 154 groundwater samples seasonally during 2014. Based on evolutionary sequence of Chebotarev, the aquifer is in the stage of SO4 + HCO3 in the north half of the plain and it has evolved into SO4 + Cl in the south half. The unusual increase in TDS and Cl? toward the western boundaries of the aquifer indicates some anomalies. These anomalies have originated from discharge of untreated wastewater of Tehran city in these areas. The studied aquifer contains four dominant groundwater types including Na–Ca–SO4 (55%), Na–Ca–HCO3 (22%), Na–Cl (13%) and Ca–Cl (10%). The spatial distributions of Na–Cl and Ca–Cl water types coincide with observed anomalies. Ionic relationships of SO4 2? versus Cl? and Na+ versus Cl? confirm that water–rock interaction and anthropogenic contribution are main sources of these ions in the groundwater. The main processes governing the chemistry of the groundwater are the dissolution of calcite, dolomite and gypsum along the flow path, and direct ion exchange. Reverse ion exchange controls the groundwater chemistry in the areas contaminated with untreated wastewater. Based on Na% and SAR, 10.3 and 27% of water samples are unsuitable for irrigation purposes, respectively. Regarding residual sodium carbonate, there is no treat for crop yields. Only 6% of water samples represent magnesium adsorption ratios more than 50% which are harmful and unsuitable for irrigation.  相似文献   

3.
Insufficient knowledge of the hydrogeochemistry of aquifers in the Central Region of Ghana has necessitated a preliminary water quality assessment in some parts of the region. Major and minor ions, and trace metal compositions of groundwater have been studied with the aim of evaluating hydrogeochemical processes that are likely to impair the quality of water in the study area. The results show that groundwater in the area is weakly acidic with mean acidity being 5.83 pH units. The dominant cation in the area is Na, followed by K, Ca, and Mg, and the dominant anion is Cl?, followed by HCO3 ? and SO4 2?. Two major hydrochemical facies have been identified as Na–Cl and Na–HCO3, water types. Multivariate statistical techniques such as cluster analysis (CA) and factor analysis/principal component analysis (PCA), in R mode, were employed to examine the chemical compositions of groundwater and to identify factors that influenced each. Q-mode CA analysis resulted in two distinct water types as established by the hydrochemical facies. Cluster 1 waters contain predominantly Na–Cl. Cluster 2 waters contain Na–HCO3 and Na–Cl. Cluster 2 waters are fresher and of good quality than cluster 1. Factor analysis yielded five significant factors, explaining 86.56% of the total variance. PC1 explains 41.95% of the variance and is contributed by temperature, electrical conductivity, TDS, turbidity, SO4 2?, Cl?, Na, K, Ca, Mg, and Mn and influenced by geochemical processes such as weathering, mineral dissolution, cation exchange, and oxidation–reduction reactions. PC2 explains 16.43% of the total variance and is characterized by high positive loadings of pH and HCO3 ?. This results from biogenic activities taking place to generate gaseous carbon dioxide that reacts with infiltrating water to generate HCO3 ?, which intend affect the pH. PC3 explains 11.17% of the total variance and is negatively loaded on PO4 3? and NO3 ? indicating anthropogenic influence. The R-mode PCA, supported by R-mode CA, have revealed hydrogeochemical processes as the major sources of ions in the groundwater. Factor score plot revealed a possible flow direction from the northern sections of the study area, marked by higher topography, to the south. Compositional relations confirmed the predominant geochemical process responsible for the various ions in the groundwater as mineral dissolution and thus agree with the multivariate analysis.  相似文献   

4.
The present study assesses the impact of coal mining on surface and groundwater resources of Korba Coalfield, Central India. Accordingly, water samples collected from various sources are analyzed for major ions, trace elements, and other mine effluent parameters. Results show that the groundwater samples are slightly acidic, whereas river water and mine water samples are mildly alkaline. Elevated concentrations of Ca2+, Na+, HCO3 ?, and SO4 2? alongside the molar ratios (Ca2++Mg2+)/(SO4 2?+HCO3 ?) <1 and Na+/Cl? >1 suggest that silicate weathering (water-rock interaction) coupled with ion exchange are dominant solute acquisition processes controlling the chemistry of groundwater in the study area. The overall hydrogeochemistry of the area is dominated by two major hydrogeochemical facies (i.e., Ca–Cl–SO4 and Ca–HCO3). Analysis of groundwater and river water quality index (GRWQI) elucidates that majority (82%) of samples are of “excellent” to “good” category, and the remaining 12% are of “poor” quality. Similarly, the effluent water quality index (EWQI) indicates that 6 out of 8 samples belong to excellent quality. Concentration of trace element constituents such as As, Zn, Cu, Cr, and Cd is found to be well within the stipulated limits for potable use, except for Fe, Mn, and Pb. Suitability of water samples for irrigation purpose, established using standard tools like Wilcox and USSL diagrams, reveal “excellent to permissible” category for majority of the samples. The present study also substantiates the effectiveness of the measures implemented for the treatment of mine effluent water.  相似文献   

5.
Chemical characteristics of groundwater in the Midyan Basin (northwestern Saudi Arabia) were investigated and evaluated. A total of 72 water samples were collected from existing shallow wells and analyzed for different elements. Two multivariate statistical methods, hierarchical cluster analysis (HCA) and principal components analysis (PCA), were applied to a subgroup of the data set in terms of their usefulness for groundwater classification, and to identify the processes controlling groundwater geochemistry. The subgroup consisted of 46 water samples out of 72 samples and 24 variables included major elements (Ca2+, Na+, Mg2+, K+, Cl?, HCO3 ?, NO3 ?, SO4 2?), minor and trace element (SiO2, Al, As, B, Ba, Cd, Cr, F, Fe, Mo, P, Pb, Sb, Sn, Ti, and V). For water samples, four geochemically distinct clusters (i.e., C1, C2, C3 and C4) have been observed by hierarchical cluster analysis. Cr, F and Pb are the dominant ions in cluster C2. Al, As, Cd, Mo, Sb and Ti are the dominant ions in cluster C3, while B, Ca, Cl, HCO3, K, Mg, Na, SO4 and V are identified as dominant ions in the cluster C4. In the PCA, a total of five components are extracted form the data set, which explained 73.37 % of the total data variability. Among them the first component reveals strong associations between As, B, Cd, Cr, F, Mo, Pb, Sb and Ti. The second component reveals the associations between Ca, Cl, HCO3, Mg, Na, SO4 and V.  相似文献   

6.
Continual expansion of population density, urbanization, agriculture, and industry in most parts of the world has increased the generation of pollution, which contributes to the deterioration of surface water quality. This causes the dependence on groundwater sources for their daily needs to accumulate day by day, which raises concerns about their quality and hydrogeochemistry. This study was carried out to increase understanding of the geological setup and assess the groundwater hydrogeochemical characteristics of the multilayered aquifers in Lower Kelantan Basin. Based on lithological data correlation of exploration wells, the study area can be divided into three main aquifers: shallow, intermediate and deep aquifers. From these three aquifers, 101 groundwater samples were collected and analyzed for various parameters. The results showed that pH values in the shallow, intermediate and deep aquifers were generally acidic to slightly alkaline. The sequences of major cations and anions were Na+ > Ca2+ > Mg2+ > K+ and HCO3? > Cl? > SO42? > CO32?, respectively. In the intermediate aquifer, the influence of ancient seawater was the primary factor that contributed to the elevated values of electrical conductivity (EC), Cl? and total dissolved solids (TDS). The main facies in the shallow aquifer were Ca–HCO3 and Na–HCO3 water types. The water types were dominated by Na–Cl and Na–HCO3 in the intermediate aquifer and by Na–HCO3 in the deep aquifer. The Gibbs diagram reveals that the majority of groundwater samples belonged to the deep aquifer and fell in the rock dominance zone. Shallow aquifer samples mostly fell in the rainfall zone, suggesting that this aquifer is affected by anthropogenic activities. In contrast, the results suggest that the deep aquifer is heavily influenced by natural processes.  相似文献   

7.
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.  相似文献   

8.
Teboursouk region, Northwestern Tunisia, is characterized by the diversity of its natural resources (petroleum, groundwater and minerals). It constitutes a particular site widely studied, especially from a tectonic stand point as it exhibits a complex architecture dominated by multi-scale synclinals and Triassic extrusions. It has typical karst landform that constitutes important water resources devoted for human consumption and agriculture activities, besides to the exploitation of the Mio-Plio-Quaternary aquifer (MPQ). Thus, hydrogeological investigations play a significant role in the assessment of groundwater mineralization and the evaluation of the used water quality for different purposes. Hence, the current study based on a combined geochemical–statistical investigation of 50 groundwater samples from the multilayered aquifer system in the study area give crucial information about the principal factors and processes influencing groundwater chemistry. The chemical analysis of the water samples showed that Teboursouk groundwater is dominantly of Ca–Mg–Cl–SO4 water type with little contribution of Ca–Mg–HCO3, Na–K–Cl–SO4 and Na–K–HCO3. The total dissolved solids (TDS) values range from 0.37 to 3.58 g/l. The highest values are located near the Triassic outcrops. Furthermore, the hydrogeochemistry of the studied system was linked with various processes such as carbonates weathering, evaporites dissolution of Triassic outcrops and anthropogenic activities (nitrate contamination). Additionally, the main processes controlling Teboursouk water system were examined by means of multivariate statistical analysis (PCA and HCA) applied in this study based on 10 physicochemical parameters (TDS, pH, SO4, HCO3, pCO2, Ca, Mg, Na, K, Cl and NO3). Two principal components were extracted from PCA accounting 61% of total variance and revealing that the chemical characteristics of groundwater in the region were acquired through carbonates and evaporite dissolution besides to nitrate contamination. Similarly, according to Cluster analysis using Ward’s method and squared Euclidean distance, groundwater from the studied basin belongs to five different groups suggesting that the geochemical evolution of Teboursouk groundwater is controlled by dissolution of carbonates minerals, chemical weathering of Triassic evaporite outcrops, cation exchange and anthropogenic activities (nitrate contamination).  相似文献   

9.
The present paper deals with major and trace elements geochemistry of the groundwater from Nalgonda district, Telangana. The study area is very important in terms of anthropogenic activity like rapid industrial, urban development, pesticides, pharmaceutical, granite polishing and agro based industries. Inductively coupled plasma mass spectrometer (ICPMS) was employed to determine the concentration of trace elements in collected groundwater samples (bore well). These probe elements were further categorized as toxic elements (Pb, As, Cd, and V), alkaline earths (Sr and Ba), alkali metals (Li, Rb), transition metals (Cr, Mo and Ni), metallic elements (Cu, Fe, Zn, Al, Co), and other non-metallic elements (Se and Si). The groundwater quality was examined in perspective of Indian as well as World Health Organization drinking water standards. Based on the analytical results, groundwater in the study area is found to be slightly alkaline in nature and very hard, the average abundance of the major cations and anions is in the order of Ca+<Na+<Mg+<K+ and Cl-<HCO3 ?<CO3 ?<SO4 ?<NO3 ?<F– respectively. The dominant hydro chemical facies of groundwater is Na+ - HCO 3 – – Cl– and Na+ - Cl– – HCO– 3 types.The results of trace elements shows that concentration of Pb, As, Cd, V in collected samples exceeding the desirable limits, and in the case of alkaline, alkali, transition, non-metallic elements, seventy per cent of the samples crossed the desirable limits, but all metallic elements viz. Cu, Fe, Zn, Al, Co is within the limits as per Indian as well as World Health Organizations drinking water standards. Factor analysis results shows that seven factors emerged as a significant contributor to the groundwater contamination is about 65.32 per cent. The spatial variation maps decipher trace elemental concentrations both geogenic and anthropogenic origin, by three zones i.e. ‘low’, ‘moderate’ and ‘high’ of the study area based on environment using Arc-GIS. High concentrations of trace elements are indicative of phenomenal rise in chemical composition and likely to have its origin from silicate weathering reactions and dissolution/precipitation processes supported by rainfall and anthropogenic activities, indiscriminate use of fertilizers/pesticides, and disposal of waste and sewage, release of reactive pollutants into the atmosphere by industries. Hence, this work is of immense societal benefit in terms of prevailing human health hazards in the study area with a direct relevance to such industrially populated regions elsewhere.  相似文献   

10.
Groundwater is a precious resource for humankind not only in Nepal but also across the globe due to its diverse functions. A total of 48 groundwater samples were collected from three villages of Nawalparasi district, Nepal, during pre-monsoon and monsoon to estimate the overall groundwater quality and to identify the sources of contamination with emphasis on arsenic (As). The average concentrations of all tested groundwater quality parameters (temp., pH, EC, ORP, Ca2+, Mg2+, Na+, K+, Cl?, F?,SO4 2?, PO4 3?, HCO3 ?, NO3 ?, Cu, Ni, Mn, Cd, Pb, Fe, Zn, Cr, and As) were well within permissible limits of WHO for drinking water, except for Ni, Cd, Pb, Cr, and As. Concentration of As ranged from 60 to 3,100 μg L?1 and 155 to 1,338 μg L?1 in pre-monsoon and monsoon, respectively. The Piper diagram of the groundwater chemistry showed groundwater of Nawalparasi belongs to Ca–Mg–HCO3 and Mg–HCO3 water type with HCO3 ? as dominant ions. As content in the study area was negatively correlated with Fe in pre-monsoon, while it was positively correlated in monsoon. Furthermore, As was negatively correlated with oxidation reduction potential suggesting reducing condition of groundwater. Principal component analysis revealed seven major factors that explained 81.996 and 83.763 % of total variance in water quality in pre-monsoon and monsoon, respectively. The variance of water quality was related mainly with the degree of water–rock interaction, mineralization, and anthropogenic inputs.  相似文献   

11.
The study of groundwater hydrogeochemistry of a hard rock aquifer system in Thoothukudi district has resulted in a large geochemical data set. A total of 100 water samples representing various lithologies like Hornblende Biotite Gneiss, Alluvium Marine, alluvium Fluvial, Quartzite, Charnockite, Granite and Sandstone were collected for two different seasons and analyzed for major ions like Ca2+, Mg2+, Na+, K+, HCO3 ?, Cl?, SO4 2?, NO3 ?, PO4 ?, F? and H4SiO4. Statistical analysis of the data has been attempted to unravel the hidden relationship between ions. Correlation analyses and factor analyses were applied to classify the groundwater samples and to identify the geochemical processes controlling groundwater geochemistry. Factor analysis indicates that sea water intrusion followed by leaching of secondary salts, weathering and anthropogenic impacts are the dominant factors controlling hydrogeochemistry of groundwater in the study area. Factor score overlay indicate major active hydrogeochemical regimes are spread throughout the Eastern, Northwestern and Southeastern parts of the study area. The dominant ions controlling the groundwater chemistry irrespective of season are Cl?, Na+, Mg2+, Ca2+, SO4 2?, K+ and NO3 ?. An attempt has also been made to note the seasonal variation of the factor representations in the study area. This study also illustrates the usefulness of statistical analysis to improve the understanding of groundwater systems and estimates of the extent of salinity/salt water intrusion.  相似文献   

12.
The present research aims to identify sources of ions and factors controlling the geochemical evolution of groundwater in an intermountain basin, comprising hill and valley fill region, of Outer Himalaya in Himachal Pradesh, India. The groundwater samples collected from 81 tubewells and handpumps are analyzed for major ions, trace metals and stable isotopes (δ18O and δD). Geochemically the dominant hydrochemical facies in the Una basin are Ca–HCO3, Ca–Mg–HCO3 and Na–Cl types at few locations. A relatively lower ionic concentration in the valley fills indicates dilution and low residence time of water to interact with the aquifer mass due to high porosity and permeability. The ionic ratios of 0.9, 0.8 and 3.8 to 5.7, respectively, for (Ca?+?Mg): HCO3, (Ca?+?Mg): (HCO3?+?SO4) and Na: Cl, suggests that ionic composition of groundwater is mainly controlled by rock weathering of, particularly by dissolution/precipitation of calcrete and calcite hosted in rock veins and Ca–Na feldspar hosted in conglomerate deposits derived from the Higher and Lesser Himalaya during the formation of Siwalik rocks. Although Na, K, NO3 and SO4 are introduced in the groundwater through agricultural practices, Na has also been introduced through ion exchange processes that have occurred during water–rock interaction, as indicated by negative CAI values. Factor analysis further suggests three major factors affecting the water chemistry of the area. The first two factors are associated with rock weathering while the third is anthropogenic processes associated with high nitrate and iron concentration. High concentrations of Fe and Mn ions that are exceeded that of WHO and BIS standards are also present at few locations. The recharge of groundwater in the Outer Himalaya is entirely through Indian Southwest Monsoon (ISM) and depleted ratios of δ18O/δD in valley region indicate infiltration from irrigation in recharging the groundwater and fractionation of isotopes of precipitation due to evaporation before infiltration. High d-excess values and inverse relation with δ18O are indicative of secondary evaporation of precipitation during recharge of groundwater.  相似文献   

13.
Groundwater is a finite resource that is threatened by pollution all over the world. Shimabara City, Nagasaki, Japan, uses groundwater for its main water supply. During recent years, the city has experienced severe nitrate pollution in its groundwater. For better understanding of origin and impact of the pollution, chemical effects and surface–groundwater interactions need to be examined. For this purpose, we developed a methodology that builds on joint geochemical analyses and advanced statistical treatment. Water samples were collected at 42 sampling points in Shimabara including a part of Unzen City. Spatial distribution of water chemistry constituents was assessed by describing Stiff and Piper diagrams using major ions concentrations. The nitrate (NO3?+?NO2–N) concentration in 45% of water samples exceeded permissible Japanese drinking level of 10 mg L??1. Most of the samples showed Ca–HCO3 or Ca–(NO3?+?SO4) water types. Some samples were classified into characteristic water types such as Na–Cl, (Na?+?K)–HCO3, (Na?+?K)–(SO4?+?NO3), and Ca–Cl. Thus, results indicated salt water intrusion from the sea and anthropogenic pollution. At the upstream of Nishi River, although water chemistry was characterized as Ca–HCO3, ion concentrations were higher than those of other rivers. This is probably an effect of disinfection in livestock farming using slaked lime. Positive correlation between NO3? and SO42?, Mg2+, Ca2+, Na+, K+, and Cl? (r?=?0.32–0.64) is evidence that nitrate pollution sources are chemical fertilizers and livestock waste. Principal component analysis showed that chemistry of water samples can be explained by three main components (PCs). PC1 depicts general ion concentration. PC2 and PC3 share influence from chemical fertilizer and livestock waste. Cluster analyses grouped water samples into four main clusters. One of these is the general river chemistry mainly affected by PC1. The others reflect anthropogenic activities and are identified by the combination of the three PCs.  相似文献   

14.
The leaching processes along the flow path and over abstraction of the alluvial aquifer, the principal aquifer in delta Tokar, by the agricultural and domestic sectors and natural factors, have led to its salinization which may be due to interaction between geological formations and adjacent brackish and saline water bodies as well as seawater transgression. The main objectives of this study are to assess the hydrochemical characteristics of the groundwater and to delineate the locations and the sources of aquifer salinization. Water samples in the project area were chemically analyzed for major cations and anions at the laboratory by the standard analytical procedures. Chemical data and water level measurements were manipulated using GIS techniques for hydro chemical and flow direction maps and piper diagram for chemical facies and SPSS software for statistical analyses such as basic statistics (mean and standard deviation) and Spearman’s correlation matrix. The general flow direction of the groundwater is from Southwest towards East and Northeast. The hydraulic gradient is relatively steeper at the apex of the delta (0.06) and amounts to 0.005 at the distal part of the delta. The average transmissivity value of the water bearing formations was found to be about 4.5?×?103 m2/s, whereas, the storage coefficient was about 0.28. A hydrochemical study identified the locations and the sources of aquifer salinization and delineated their areas of influence. The investigation indicates that the aquifer water quality is significantly modified as groundwater flows from the southwestern parts of the study area, where the aquifer receives its water by lateral underflow from Khor Baraka flood plain, to the central and northeastern parts, with few exceptions of scattered anomalous concentration pockets in the deltaic plain. Significant correlation between TDS and/or EC with the major components of Na+, Cl?, and SO 4 ?2 ions is an indication of seawater influence on the groundwater salinity. Moreover, Cl?, SO 4 2? , and Na+ are predominant ions followed by Ca2+ and HCO 3 ? . Hence, four types of groundwater can be chemically distinguished: Na–Ca–SO4–Cl– facies, Na–Cl–SO4–HCO3– facies, Na–Ca–Mg–SO4–Cl–HCO3 facies, and Na–Ca–Mg–Cl–SO4 facies. The processes that govern changes in groundwater composition as revealed by chemical and statistical analyses are mainly associated with over-abstraction, biodegradation, marine intrusions, and carbonate saturation.  相似文献   

15.
There are 59 springs at the Gevas–Gurp?nar–Güzelsu basins, 38 of these springs emerge from the fractured karst aquifers (recrystallized limestone and travertine) and 21 emerge from the Yuksekova ophiolites, K?rkgeçit formation and alluvium. The groundwater samples collected from 38 out of the total of 59 springs, two streams, one lake and 12 wells were analyzed physico-chemically in the year 2002. EC and TDS values of groundwater increased from the marble (high altitude) to the ophiolites and alluvium (toward Lake Van) as a result of carbonate dissolution and connate seawater. Five chemical types of groundwater are identified: Ca–Mg–HCO3, Mg–Ca–HCO3, Mg–Na–HCO3, Na–Ca–HCO3 and Mg–Ca–Na–HCO3. The calculations and hydrochemical interpretations show that the high concentrations of Ca2+, Mg2+ and HCO3 ? as predominant ions in the waters are mainly attributed to carbonate rocks and high pCO2 in soil. Most of the karst springs are oversaturated in calcite, aragonite and dolomite and undersaturated in gypsum, halite and anhydrite. The water–rock interaction processes that singly or in combination influence the chemical composition of each water type include dissolution of carbonate (calcite and dolomite), calcite precipitation, cation exchange and freshening of connate seawater. These processes contribute considerably to the concentration of major ions in the groundwater. Stable isotope contents of the groundwater suggest mainly direct integrative recharge.  相似文献   

16.
An attempt has been made to delineate the hydrochemistry for a small island based on the major ions and heavy metal concentrations. In this investigation, six sampling campaigns were conducted to measure the concentrations of major ions (Ca, Mg, Na, K, HCO3, Cl, and SO4) and heavy metals (Zn, Cr, Pb, Mn, As, and Cu) in groundwater samples collected from seven sampling stations (boreholes) located on Kapas Island, Terengganu, Malaysia. The distribution of major ions is illustrated by a piper plot where Ca–HCO3 is the dominant type. In addition, the concentrations of heavy metals demonstrate that Mn shows as being the highest concentrated heavy metal in the groundwater sampled in the sampling campaigns; the average Mn content in groundwater sampled was 54.05 μg/L. However, a comparison of the heavy metal (Mn, Cr, Zn, As, Pb, and Cu) concentrations in groundwater samples with the Drinking Water Quality Standard prescribed by World Health Organization reveals that none of these heavy metals exceeded the recommended threshold limits. The principal component analyses (PCA) extracted four components that control the groundwater chemistry. Components 1 and 2 from the PCA analyses extracted approximately 52.11 % of the total variance, which represent the heavy metals (As and Mn) and physical parameters (pH, redox potential, electrical conductivity, temperature, and total dissolved solids). Based on the output of the PHREEQC hydrogeochemical software, several species of heavy metals exist, in which the dominant species found are Mn2+, PbCO3, Cu(OH)2, and Zn+.  相似文献   

17.
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18.
Water samples from the river network and from some shallow and brackish springs located in a tectonic window of the northern Apennines of Italy were studied in the frame of a comprehensive hydrogeological investigation in order to better understand the origin and the mixing processes between the two water types noticed also in previous studies (Ca–HCO3 and Na–Cl). A sampling campaign covering the drought period during year 2010 was planned to gather electric conductivity, temperature and redox potential data along the river network and on groundwater occurrences located inside the tectonic structure. Additionally, eight water samples were collected for hydrochemical (major anions and cations: Na+, K+, Ca2+, Mg2+, HCO3 ?, Cl?, SO4 2? and trace ion Btot) and isotopic (δ18O, δ2H, 3H) analyses and compared with other eighteen samples from shallow and brackish springs collected near the study site during the period 2005–2012. Moreover, river discharge and water balance estimations were carried out. Results confirmed the presence of old Na–Cl water with salinity progressively increasing up to 5.5 g l?1 at the northern termination of the tectonic window. These values are in agreement with the ions contents of the most mineralized spring (Macognano spring: salinity of 7.6 g l?1), which has been considered as having the deepest and longest flow-path. Stable isotopes and trace ions contents are consistent with rainfall and snowmelt water mixed with brines associated with a hydrocarbon reservoir hosted at depth. Considering as end-member the more mineralized Na–Cl water, a cumulate inflow in the range of 12.9 ± 5.9 l s?1 has been estimated. This aliquot is released into the river network with different mixing proportions by the groundwater occurrences discharging from the autochthonous flysch unit.  相似文献   

19.
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.  相似文献   

20.
Hydogrochemical investigation of groundwater resources of Paragraph district has been carried out to assess the solute acquisition processes and water quality for domestic and irrigation uses. Fifty-five groundwater samples were collected and analyzed for pH, electrical conductivity, total dissolved solids, hardness, major anions (F?, Cl?, NO3, HCO3 ?, SO4 2?) and cations (Ca2+, Mg2+, Na+, K+). Study results reveal that groundwater of the area is alkaline in nature and HCO3 ?, Cl?, Mg2+, Na+ and Ca2+ are the major contributing ions to the dissolved solids. The hydrogeochemical data suggest that weathering of rock forming minerals along with secondary contributions from agricultural and anthropogenic sources are mainly controlling the groundwater composition of Pratapgarh district. Alkaline earth metals (Ca2++Mg2+) exceed alkalis (Na++K+) and weak acid (HCO3 ?) dominate over strong acids (Cl?+SO4 2?) in majority of the groundwater samples. Ca-Mg-HCO3 and Ca-Mg-Cl-HCO3 are the dominant hydrogeochemical facies in the groundwater of the area. The computed saturation indices demonstrate oversaturated condition with respect to dolomite and calcite and undersaturated with gypsum and fluorite. A comparison of groundwater quality parameters in relation to specified limits for drinking water shows that concentrations of TDS, F?, NO3 ? and total hardness exceed the desirable limits in many water samples. Quality assessment for irrigation uses reveal that the groundwater is good for irrigation. However, values of salinity, sodium adsorption ratio (SAR), residual sodium carbonate (RSC), %Na and Kelley index are exceeding the prescribed limit at some sites, demanding adequate drainage and water management plan for the area.  相似文献   

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