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1.
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.  相似文献   

2.
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.  相似文献   

3.
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.  相似文献   

4.
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.  相似文献   

5.
In the light of progressive depletion of groundwater reservoir and water quality deterioration of the Neyveli basin, an investigation on dissolved major constituents in 25 groundwater samples was performed. The main objective was detection of processes for the geochemical assessment throughout the area. Neyveli aquifer is intensively inhabited during the last decenniums, leading to expansion of the residential and agricultural area. Besides semi-aridity, rapid social and economic development stimulates greater demand for water, which is gradually fulfilled by groundwater extraction. Groundwaters of the study area are characterized by the dominance of Na?+?K over Ca?+?Mg. HCO3 was found to be the dominant anion followed by Cl and SO4. High positive correlation was obtained among the following ions: Ca–Mg, Cl–Ca,Mg, Na–K, HCO3–H4SiO4, and F–K. The hydrochemical types in the area can be divided into two major groups: the first group includes mixed Ca–Mg–Cl and Ca–Cl types. The second group comprises mixed Ca–Na–HCO3 and Ca–HCO3 types. Most of the groundwater samples are within the permissible limit of WHO standard. Interpretation of data suggests that weathering, ion exchange reactions, and evaporation to some extent are the dominant factors that determine the major ionic composition in the study area.  相似文献   

6.
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.  相似文献   

7.
Aquifer-based groundwater quality assessment offers critical insight into the major hydrochemical processes, and aids in making groundwater resources management decisions. The Texas Rolling Plains (TRP), spanning over 22 counties, is a major agro-ecological region in Texas from where highest groundwater nitrate (NO3 ?) levels in the state have been reported. In this study, we present a comparative assessment of major hydrochemical facies pertaining to NO3 ? contamination and a host of species such as sulfate (SO4 2?), chloride (Cl?), and total dissolved solids (TDS) in different water use classes in the Seymour and Blaine aquifers, underlying the TRP. Aquifer-stratified groundwater quality information from 1990 to 2010 was obtained from the Texas Water Development Board and aggregated over decadal scale. High groundwater salinization was found in the municipal water use class in the Blaine aquifer with about 100, 87 and 50 % of observations exceeding the secondary maximum contaminant level for TDS, SO4 2?, and Cl?, respectively in the 2000s (2000–2010). The NO3-contamination was more alarming in the Seymour aquifer with 82 and 61 % of observations, respectively, exceeding the maximum contaminant level (MCL) in the irrigation and municipal water use classes in the 2000s. Salinization was more influenced by SO4 2? and Cl? in the Blaine aquifer and by NO3 ? in the Seymour aquifer. High NO3 ? (>MCL) observations in the Seymour aquifer occurred in the Ca–HCO3 and Ca–Mg–HCO3 facies, the domains of fresh water recharge and anthropogenic influences (e.g., agricultural activities, waste disposal). High SO4 2?, Cl? and TDS observations in the Blaine aquifer dominated the Ca–Cl, Na–Cl, and mixed Ca(Mg)–SO4(Cl) facies indicating evaporite dissolution, mixing and solute exchange, and lack of fresh recharge.  相似文献   

8.
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.  相似文献   

9.
Groundwater qualities of coastal aquifers in the Ottapidaram taluk of Thoothukudi district, Tamil Nadu have been extensively monitored in post monsoon seasons in 2014 to assess its suitability in relation to domestic and drinking uses in four regions (N-S-EW). 34 groundwater samples were analyzed for various physicochemical attributes like pH, electrical conductivity (EC), Total dissolved solid (TDS), Na, K, Ca, Mg, Cl, HCO3, CO3, SO4, NO3, PO4. Most of these parameters fall under not permissible limits. The western part of the study area is highly polluted from K, Cl, HCO3 due to industrial/agriculture activity. The southern part is less polluted compared to other region. Hydrogeochemical processes controlling the water chemistry (Gibbs) indicates that most of groundwater samples fall at rock-weathering supremacy zone. Geochemical processes and temporal variation in the groundwater in this area are influenced by evaporation processes, ion exchange and dissolution of minerals. Major cation and anion ionic interaction indicate that weathering reactions have an inconsequential role in the hydrochemical processes of the shallow groundwater system. As a result of the hydrogeochemical analysis, seawater intrusion, aquifer rock weathering, sewer leakage are the overriding factors that determine the major ionic composition. The appropriate management plan is necessary to preserve precious groundwater resources.  相似文献   

10.
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   

11.
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   

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.
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14.
Correct identification of water inrush sources is particularly important to prevent and control mine water disasters. Hydrochemical analysis, Fisher discriminant analysis, and geothermal verification analysis were used to identify and verify the water sources of the multi‐aquifer groundwater system in Gubei coal mine, Anhui Province, North China. Results show that hydrochemical water types of the Cenozoic top aquifer included HCO3–Na+K–Ca, HCO3–Na+K–Mg and HCO3–Na+K, and this aquifer was easily distinguishable from other aquifers because of its low concentration of Na++K+ and Cl–. The Cenozoic middle and bottom aquifers, the Permian fissure aquifer, and the Taiyuan and Ordovician limestone aquifers were mainly characterized by the Cl–Na+K and SO4–Cl‐Na+K or HCO3–Cl–Na+K water types, and their hydrogeochemistries were similar. Therefore, water sources could not be identified via hydrochemical analysis. Fisher model was established based on the hydrogeochemical characteristics, and its discrimination rate was 89.19%. Fisher discrimination results were improved by combining them with the geothermal analysis results, and this combination increased the identification rate to 97.3 % and reasonably explained the reasons behind two water samples misjudgments. The methods described herein are also applicable to other mines with similar geological and hydrogeological conditions in North China.  相似文献   

15.
The present study deals with the hydrochemical characteristics of groundwater in the upper catchment of Wadi Fatimah basin. The analysis of data indicated strongly that the chloride and sulfate in the groundwater are mainly of marine origin, concentrated by high evaporation processes. Flushing is the most important factor that modifies the ionic concentrations and almost stands for the short-term variation in groundwater chemistry. Weathering reactions of the rock-forming minerals take place under relatively high PCO2 condition in water and soil zone; it can be an important long-term neutralization process. It is accounted as a contributor for Ca and Mg ions in the groundwater. Using the chloride method the recharge rate has been estimated at 72 mm yr–1.  相似文献   

16.
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.  相似文献   

17.
Source, type, and quantity of various components of groundwater, as well as their spatial and temporal variations were determined by different hydrochemical methods in the alluvial aquifer of the upper Rhone River valley, Bois de Finges, Wallis Canton, Switzerland. The methods used are hydrochemical modeling, stable-isotope analysis, and chemical analysis of surface water and groundwater. Sampling during high- and low-water periods determined the spatial distribution of the water chemistry, whereas monthly sampling over three years provided a basis for understanding seasonal variability. The physico-chemical parameters of the groundwater have spatial and seasonal variations. The groundwater chemical composition of the Rhone alluvial aquifer indicates a mixing of weakly mineralized Rhone River water and SO4-rich water entering from the south side of the valley. Temporal changes in groundwater chemistry and in groundwater levels reflect the seasonal variations of the different contributors to groundwater recharge. The Rhone River recharges the alluvial aquifer only during the summer high-water period. Electronic Publication  相似文献   

18.
The Çeltikçi (Burdur) plain is located in the southwest of Turkey and is a semi-closed basin. Groundwater is densely used as drinking, irrigation and domestic water in the plain. Hydrogeochemical processes controlling groundwater chemistry and geochemical assessment of groundwater were investigated in the Çeltikçi (Burdur/Turkey) plain. In this study, groundwater samples for two seasons were analyzed and major ion chemistry of groundwater was researched to understand the groundwater geochemistry. Two major hydrochemical facies (Ca–HCO3 and Ca–Mg–HCO3) were determined in the area. Various graphical plots and multivariate statistical analysis were used for identifying the occurrence of different geochemical processes. In the study area, weathering is one of the key geochemical processes which controlled the solute concentration in groundwater. Chemical indexes such as sodium adsorption ratio, %Na, residual sodium carbonate, magnesium hazard and permeability index were calculated and results show that groundwater is suitable for irrigation purpose except for permeability index values. Concentrations of Mn, NO3 and total hardness exceed the prescribed limits of WHO and are the major limiting parameters of groundwater use for potable and domestic purposes.  相似文献   

19.
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   

20.
《Applied Geochemistry》2001,16(9-10):1179-1192
The Cabra-Alcaide karstic massif situated in the south of Spain constitutes an important part of the so-called Natural Park of the Subbetic Sierras. This aquifer system is drained by various springs which supply a population of some 100,000 inhabitants. The feed areas of these springs show very different characteristics with respect to their geological structure, size of the drainage area, thickness of the vadose zone, elevation and degree of karstification. In addition, the carbonate rocks lie over a clayey substratum which contains large masses of intercalated evaporites. Due to these conditions, the hydrochemical composition of the springs is relatively variable. In this study a hydrogeochemical characterization of the aquifer in both space and time is undertaken and the factors that determine it are discussed. To achieve this, 19 monthly samples were taken from the 6 most significant springs of the hydrogeological system. The commencement of sampling coincided with the transition from a period of several years of severe drought and a very wet two-year period, which amplified considerably the hydrochemical and hydrodynamic response of the springs to the recharge. Identification of hydrogeochemical processes was performed by studying hydrographs, the temporal evolution of physico-chemical parameters, ionic ratios (mainly Mg/Ca) and by means of simple and multivariate statistical analyses. The saturation status was established using the WATEQF program and the mass transfer was quantified using PHREEQC. With the exception of the epikarstic subsystem (i.e. the Zarza spring), the majority of the results indicate that the aquifer exhibits a diffuse flow model, in which piston flow phenomena are seen, closely linked to the most intense precipitation. Along the direction of flow hydrochemical trends are seen as the water type changes from Ca–HCO3 to Ca–Mg–HCO3; at the same time enrichment in some ions, derived from the dissolution of evaporitic minerals of the impermeable substratum, and dedolomitization processes occur. In this way, almost 90% of the water samples were oversaturated in calcite, the majority of cases being a consequence of the dissolution of the gypsum of the substratum. Only in the epikarstic springs can it be considered that the oversaturation in calcite is due to loss of CO2 from the emerging groundwater. It is concluded that hydrodynamic aspects together with hydrogeochemical characteristics need to be taken into account to correctly explain the hydrochemical evolution of the karstic springs. Moreover, the use of both approaches permits a more accurate establishment of the degree of aquifer karstification, which in turn needs to be known in order to assess its vulnerability to contamination and to protect recharge zones.  相似文献   

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