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1.
This work present results of the hydrochemical and isotopic studies on groundwater samples from the study area. Chemical and environmental isotope data are presented and discussed in terms of the origin of dissolved species and of groundwater. All of the investigated groundwater are categorized into two chemical types: low and relatively high mineralized waters type. Interpretation of chemical data, based on both thermodynamic calculations and stability diagrams, suggests that the chemical evolution of groundwater is primarily controlled by water-rock interactions. Interpretation of 18O and 2H suggests that the recharge of the investigated groundwater may result from differents mechanisms  相似文献   

2.
The Middle Awash basin is an arid region in Ethiopia where surface waters are scarce and local communities are dependent on groundwater resources for water supply. The complex hydrogeological system of this basin has been conceptualized. Multivariate statistical analysis of hydrochemical variables and water isotopes were used to study the rock?Cwater interaction, geochemical reaction processes and the hydrological link between aquifers. Groundwaters from aquifers of the high-rainfall plateau bounding the rift are slightly mineralized, as well as depleted in ??18O and ??D, and contain 3H above 0.8?TU. This suggests a low degree of rock?Cwater interaction and that groundwater is under recharge from heavy rain that falls on surrounding highlands. On the other hand, groundwaters from aquifers of the rift floor are highly mineralized and show slight enrichment in ??18O and ??D with positive oxygen shift, but contain 3H below 0.8?TU. The positive oxygen shift in rift floor groundwaters may be caused by the isotopic exchange of oxygen between groundwater and aquifer materials during rock?Cwater interaction, whereas the low 3H content could be due to the decay of tritium along relatively long flow paths. The approach utilized in this study may be applicable to understanding hydrogeochemical processes in other complex volcanic terrains.  相似文献   

3.
A study of the hydrogeochemical processes in the Morsott-El Aouinet aquifer was carried out with the objective of identifying the geochemical processes and their relation with groundwater quality as well as to get an insight into the hydrochemical evaluation of groundwater. The high salinity coupled with groundwater level decline pose serious problems for current irrigation and domestic water supplies as well as future exploitation. A combined hydrogeologic and isotopic investigation have been carried out using chemical and isotopic data to deduce a hydrochemical evaluation of the aquifer system based on the ionic constituents, water types, hydrochemical facies and factors controlling groundwater quality. The ionic speciation and mineral dissolution/precipitation was calculated by WATEQF package software. The increase in salinity is related to the dissolution and/or precipitation processes during the water–rock interaction and to the cationic exchange reactions between groundwater and clay minerals. The isotopic analysis of some groundwater samples shows a similarity with the meteoric waters reflect their short residence time and a lowest evaporation phenomenon of infiltrated groundwater.  相似文献   

4.
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   

5.
Geochemical characterization of groundwater from an arid region in India   总被引：3，自引：1，他引：2  
A study on the geochemical processes in arid region of western India (Kachchh district) was carried out using major, minor, trace metal data and isotopic composition (δ2H, δ18O) of groundwaters. Results indicate that the distribution of chemical species in groundwater of this district is controlled by leaching of marine sediments, dissolution of salts in root zone and incongruent dissolution of carbonate minerals. Common inorganic contaminants such as fluoride, nitrate and phosphate are within drinking water permissible limits. However, most of the samples analyzed contain total dissolved salts more than desirable limits and fall in doubtful to unsuitable category with regard to irrigational purpose. Trace metal data indicates no contamination from toxic elements such as arsenic and lead. An increased salt content is observed in groundwater at shallower depths indicating mixing with surface water sources. The chemical characteristics of the groundwater have found to be strongly dependent on the local lithological composition. Environmental isotopic data indicates that the groundwater is of meteoric origin and has undergone limited modification before its recharge. The processes responsible for observed brackishness are identified using chemical and isotope indicators, which are in agreement with subsurface lithology and hydrochemistry. These data though represent hydrochemical scenario of 2001 can still be used for understanding the long-term fluctuations in water chemistry and would be quite useful for the planners in validating groundwater quality models.  相似文献   

6.
《Applied Geochemistry》2001,16(7-8):745-758
The physical–chemical characteristics of the groundwater in the Baza–Caniles detrital aquifer system indicate that a wide diversity of hydrochemical conditions exists in this semiarid region, defining geochemical zones with distinct groundwater types. The least mineralized water is found closest to the main recharge zones, and the salinity of the water increases significantly with depth towards the center of the basin. Geochemical reaction models have been constructed using water chemistry data along flow paths that characterize the different sectors of the aquifer system, namely: Quaternary aquifer, unconfined sector and shallow and deep confined sectors of the Mio–Pliocene aquifer. Geochemical mass–balance calculations indicate that the dominant groundwater reaction throughout the detrital system is dedolomitisation (dolomite dissolution and calcite precipitation driven by gypsum dissolution); this process is highly developed in the central part of the basin due to the abundance of evaporites. Apart from this process, there are others which influence the geochemical zoning of the system. In the Quaternary aquifer, which behaves as a system open to gases and which receives inputs of CO2 gas derived from the intensive farming in the area, the interaction of the CO2 with the carbonate matrix of the aquifer produces an increase in the alkalinity of the water. In the shallow confined sector of the Mio–Pliocene aquifer, the process of dedolomitisation evolves in a system closed to CO2 gas. Ca2+/Na+ cation exchange and halite dissolution processes are locally important, which gives rise to a relatively saline water. Finally, in the deep confined sector, a strongly reducing environment exists, in which the presence of H2S and NH+4 in the highly mineralized groundwater can be detected. In this geochemical zone, the groundwater system is considered to be closed to CO2 gas proceeding from external sources, but open to CO2 from oxidation of organic matter. The geochemical modeling indicates that the chemical characteristics of this saline water are mainly due to SO4 dissolution, dedolomitisation and SO4 reduction, coupled with microbial degradation of lignite.  相似文献   

7.
The phreatic aquifer beneath the Pampean plain, in eastern central Argentina, constitutes a relevant source of water supply in the area. The objective of this work was to assess the significance of the cation exchange processes in the hydrochemical evolution of this aquifer, based on a study case located in the middle and upper basin of the El Pescado creek. Results indicate that Ca2+/Na+ exchange is the main process determining the evolution of groundwater from the recharge areas (Ca–HCO3) towards the local discharge areas (Na–HCO3), as well as representing a source of Na+ contribution to the water in the aquifer. This hydrochemical characteristic is central to the identification of local discharge areas within a plain environment which extends regionally. The ion exchange capacity of these discharge areas has environmental importance, due to its influence on groundwater quality and potential groundwater uses. These results may be applied to any aquifer sharing similar hydrogeological characteristics.  相似文献   

8.
The identification of sources and behavior of contaminants is important to control and manage groundwater quality of aquifer systems in urban areas. In this study, hydrogeochemistry of major constituents and stable isotope ratios of nitrate in groundwater were determined to identify contamination sources and transformation processes occurring in soils and deeper groundwater of Beijing with intense human activities. The nitrogen and oxygen isotopic compositions of nitrate in pore water extracts from groundwater samples indicate at least three potential sources of nitrate in groundwaters at Beijing. Stable isotope analyses from this study site, which has atmospheric, chemical fertilizer and human waste nitrate sources, provide a tool to distinguish nitrate sources in a confined aquifer where concentrations alone do not. These data indicate that the most common sources of high nitrate concentrations in groundwater at Beijing are wastewater and denitrification process occurred specially in the Central area. NO3–N and cation and anion concentrations (Ca2+, Mg2+ Cl? and SO 4 2 ) showed strong correlations indicating that they originated from the same sources. This study demonstrates that a thorough evaluation of hydrodynamic and hydrochemical parameters with dual isotopes of NO3 ? constitutes an effective approach for identifying sources and transformation processes of NO3 ? in deeper groundwater systems.  相似文献   

9.
The demand for water is rapidly increasing in Egypt, because of high population and agriculture production growth rate, which makes research of water resources necessary. The regional multi-aquifer system of the Miocene–Pleistocene age is discharged in Wadi El Natrun area. Intensive aquifer overexploitation and agricultural development in the area are related to groundwater quality deterioration. Hydrochemical and hydrogeological data was evaluated to determine the groundwater origin and quality in the south-eastern part of wadi, which appears to be more significant for water supply owing to lower groundwater salinity. The dominance of the high mineralised Cl groundwater type was found; however, also less mineralised SO4 and HCO3 types were identified there. Based on the ion relations, halite and gypsum dissolution and ion exchange are the most important hydrochemical processes forming the groundwater chemical composition. The Cl dominated groundwater matches the discharge part of the regional hydrogeological system. Contrary, the presence of HCO3 and SO4 hydrochemical types corresponds to the infiltration and transferring parts of the hydrogeological system indicating the presence of zones conducting low mineralised groundwater. The discharge area of the over-pumped aquifer in Wadi El-Natrun lies 23 m beneath the sea level with the shoreline being at the distance of 100 km, thus there is a real risk of seawater intrusion. Using the hydrochemical facies evolution diagram, four samples in the centre of the discharge area indicate advanced seawater intrusion. The zones of the highest demand for groundwater quality protection were indicated based on a spatial pattern of hydrogeochemical composition.  相似文献   

10.
In order to identify the origin of the main processes that affect the composition of groundwater in a karstic aquifer, a hydrogeochemical and isotopic study was carried out of water from numerous observation wells located in Sierra de Gador, a semiarid region in SE Spain. Several natural and anthropogenic tracers were used to calculate groundwater residence time within this complex aquifer system. Analysis of major ions enabled the principal geochemical processes occurring in the aquifer to be established, and the samples were classified into four distinctive solute groups according to this criterion. Dissolution of carbonate rocks determines the chemical composition of less mineralized water. In another group, the concurrent dissolution of dolomite and precipitation of calcite in gypsum-bearing carbonate aquifer, where the dissolution of relatively soluble gypsum controls the reaction, are the dominant processes. Marine intrusion results in highly mineralized waters and leads to base exchange reactions. The groundwater enrichment of minor and trace elements allowed classification of the samples into two classes that are linked to different flow patterns. One of these classes is influenced by a slow and/or deep regional flow, where the temperature is generally elevated. The influence of sulphate reduces by up to 40 % the barium concentration due to the barite precipitation. Isotope data (T, 14C) confirm the existence of recent local flows, and regional flow system, and ages of ground water may reach 8000 years. The importance of gypsum dissolution in this aquifer is proved by the δ34S content.  相似文献   

11.
A multi-tracer approach has been carried out in the Sbeïtla multilayer aquifer system, central Tunisia, to investigate the geochemical evolution, the origin of groundwaters and their circulation patterns. It involves statistical data analysis coupled with the definition of the hydrochemical and isotopic features of the different groundwaters. Principal Components Analysis (PCA) of geochemical data used in conjunction with bivariate diagrams of major and trace elements indicate that groundwater mineralization is mainly controlled by water-rock interaction and anthropogenic processes in relation to return flow of irrigation waters. The PCA of isotopic data and bivariate conventional diagrams of stable and radiogenic isotopes i.e. δ18O vs. δ2H and δ18O vs. 14C provide valuable information about the origin and the circulation patterns of the different groundwater groups. They permit classifying groundwaters into three groups. The first group is characterized by low 3H concentrations, low 14C activities and depleted stable isotope contents. It corresponds to an old end-member in relation with palaeoclimatic recharge which occurred during the Late Pleistocene and the Early Holocene humid periods. The second group is distinguished by high to moderate 3H concentrations, high 14C activities and enriched heavy isotope signatures. It corresponds to a modern end-member originating from a mixture of post-nuclear and present-day recharge in relation to return flow of irrigation waters. The third group is characterized by an average composition of stable and radiogenic isotope signatures. It provides evidence for the mixing between the upward moving palaeoclimatic end-member and the downward moving present-day end-member.  相似文献   

12.
Ayadi  Rahma  Trabelsi  Rim  Zouari  Kamel  Saibi  Hakim  Itoi  Ryuichi  Khanfir  Hafedh 《Hydrogeology Journal》2018,26(4):983-1007

Major element concentrations and stable (δ18O and δ2H) and radiogenic (3H and 14C) isotopes in groundwater have proved useful tracers for understanding the geochemical processes that control groundwater mineralization and for identifying recharge sources in the semi-arid region of Sfax (southeastern Tunisia). Major-ion chemical data indicate that the origins of the salinity in the groundwater are the water–rock interactions, mainly the dissolution of evaporitic minerals, as well as the cation exchange with clay minerals. The δ18O and δ2H relationships suggest variations in groundwater recharge mechanisms. Strong evaporation during recharge with limited rapid water infiltration is evident in the groundwater of the intermediate aquifer. The mixing with old groundwater in some areas explains the low stable isotope values of some groundwater samples. Groundwaters from the intermediate aquifer are classified into two main water types: Ca-Na-SO4 and Ca-Na-Cl-SO4. The high nitrate concentrations suggest an anthropogenic source of nitrogen contamination caused by intensive agricultural activities in the area. The stable isotopic signatures reveal three water groups: non-evaporated waters that indicate recharge by recent infiltrated water; evaporated waters that are characterized by relatively enriched δ18O and δ2H contents; and mixed groundwater (old/recent) or ancient groundwater, characterized by their depleted isotopic composition. Tritium data support the existence of recent limited recharge; however, other low tritium values are indicative of pre-nuclear recharge and/or mixing between pre-nuclear and contemporaneous recharge. The carbon-14 activities indicate that the groundwaters were mostly recharged under different climatic conditions during the cooler periods of the late Pleistocene and Holocene.

  相似文献   

13.
《Applied Geochemistry》2000,15(6):819-832
In this paper the groundwater in-situ generation of dissolved organic carbon (DOC) is discussed based on the origin of groundwaters, their physico-chemical and isotopic properties, chemical composition and the dissolved inorganic carbon (DIC) concentration and its 13C content. Three aquifer systems are investigated. Two of these have relatively well defined hydrological and geochemical conditions (Fuhrberg and Munich) and are used as reference systems. The third aquifer (Gorleben) is a complex system containing DOC concentrations up to 200 mg C/L in deep groundwaters. From this aquifer system 19 groundwaters from different hydrogeochemical conditions are analyzed. The in-situ generation of DOC is found to occur in conjunction with the microbiologically mediated mineralization of sedimentary organic carbon (SOC). Thereby, SO4 is reduced and phosphate is released into the groundwater. Where SO4 is depleted, the mineralization of SOC occurs via fermentation, resulting in CH4 generation.  相似文献   

14.
A hydrogeochemical approach has been carried out in the Mio-Plio-Quaternary aquifer system of northern Sfax to investigate the geochemical evolution, the origin of groundwaters and their circulation patterns. The groundwater samples collected from different wells seem to be dominated by sodium chloride type to sulphate chloride type. Detail analysis of chemical data including the thermodynamic calculations was used to assess that the chemical evolution of groundwater is primarily controlled by water–rock interactions. The values of sodium absorption ratio and electrical conductivity of the groundwater were plotted in the US Salinity Laboratory diagram for irrigation water. Most of the water samples in northern Sfax fall in the fields of C4S1, C4S2 and C4S3 indicating very high salinity and medium to high sodium alkalinity hazard. Thus, groundwater quality is ranging between doubtful to unsuitable for irrigation uses under normal condition, and further action for salinity control is required in remediating such problem. Principal component analysis of geochemical data used in conjunction with bivariate diagrams of major elements indicates that groundwater mineralization is mainly controlled by (1) water–rock interaction processes, (2) anthropogenic process in relation with return flow of NO3-rich irrigation waters and (3) domestic discharges.  相似文献   

15.
The evaluation of the long-term effects of seawater intrusion into the aquifers due to negative water balance and nitrate pollution of drinking-water quality due to human activities requires detailed knowledge of both the transport of the chemical constituents and the geochemical processes within aquifers. Hydrogeological and hydrochemical studies in the unconfined aquifer of Malia have provided the necessary data to define the areas at increased risk from these phenomena. The solution of the second Fick's low under given boundary conditions gave an estimate of the propagation of groundwater pollution by NO3 –. Additionally, in order to simulate the ion concentration changes during a period, for example a period of positive water balance or refreshening, groundwater transport and cation exchange reactions were modelled using the code PHREEQM. Received: 25 July 1997 · Accepted: 4 November 1997  相似文献   

16.
Hydrochemical and isotopic study of Miocene and Mio-Plio-Quaternary (M-P-Q) aquifers in Wadi El Hechim?CGaraa Hamra basin, Central Tunisia was undertaken in order to investigate recharge mode and processes leading to mineralization of groundwater as well as interaction between both systems. The results revealed striking differences between the two aquifer systems. While the Miocene aquifer contains recently recharged waters with generally low mineralization (around 0.5?g?L?1), stemming mainly from dissolution of carbonate minerals, the M-P-Q aquifer reveals TDS values reaching 3?g?L?1, controlled mainly by dissolution of evaporitic minerals. Isotopic data indicate that the Miocene aquifer contains water recharged in past several decades (bomb tritium and bomb radiocarbon detected). The M-P-Q system appears to be much slower, with time scales of groundwater flow possibly reaching some thousands of years. Sharp discontinuity of hydrochemical and isotope characteristic of groundwater observed across the major tectonic fault separating the Miocene and M-P-Q aquifers supports the idea of very limited (if any) hydraulic interconnection between both studied systems. This in turn calls for revision of existing conceptual models of groundwater flow in the region postulating significant groundwater fluxes crossing the fault in the direction of M-P-Q aquifer and adjacent aquifers in the Wadi al Fakka plain.  相似文献   

17.
Significant upward movement of mineralized water takes place in the Puebla aquifer system. Preferential groundwater flow paths related to the geological structure and the lowering of the potentiometric surface are suspected to be the prime factors for this intrusion. A combined approach of geochemical and isotope analyses was used to assess the sources of salinity and processes that are controlling the changes in groundwater chemical composition in the Puebla aquifer. Geochemical and isotope data indicate that the likely source of increased solutes is mineralized water from the dissolution of evaporites of the Cretaceous age at the base of the Upper deep aquifer, which is deeper than the intakes of the shallow wells. Dedolomitization and cation exchange seems also to occur along flow paths where sulphate concentrations tend to increase. The deep regional flow paths controls the chemical stratification of groundwater in response to decreased heads through interconnecting vertical and horizontal pathways, such as in the Fosa Atlixco. The results also suggest that high sulphate concentrations originating in the Lower deep aquifer are currently affecting shallow production wells. It is concluded that hydrodynamic aspects together with hydrogeochemical characteristics need to be taken into account to correctly explain the hydrochemical evolution in the stratified aquifer.  相似文献   

18.
A 4-yr study of spatial and temporal variability in the geochemistry of vadose groundwaters from caves within the Edwards aquifer region of central Texas offers new insights into controls on vadose groundwater evolution, the relationship between vadose and phreatic groundwaters, and the fundamental influence of soil composition on groundwater geochemistry. Variations in Sr isotopes and trace elements (Mg/Ca and Sr/Ca ratios) of dripwaters and soils from different caves, as well as phreatic groundwaters, provide the potential to distinguish between local variability and regional processes controlling fluid geochemistry, and a framework for understanding the links between climatic and hydrologic processes.The Sr isotope compositions of vadose cave dripwaters (mean 87Sr/86Sr = 0.7087) and phreatic groundwaters (mean 87Sr/86Sr = 0.7079) generally fall between values for host carbonates (mean 87Sr/86Sr = 0.7076) and exchangeable Sr in overlying soils (mean 87Sr/86Sr = 0.7088). Dripwaters have lower Mg/Ca and Sr/Ca ratios, and higher 87Sr/86Sr values than phreatic groundwaters. Dripwater 87Sr/86Sr values also inversely correlate with both Mg/Ca and Sr/Ca ratios. Mass-balance modeling combined with these geochemical relationships suggest that variations in fluid compositions are predominantly controlled by groundwater residence times, and water-rock interaction with overlying soils and host aquifer carbonate rocks. Consistent differences in dripwater geochemistry (i.e., 87Sr/86Sr, Mg/Ca, and Sr/Ca) between individual caves are similar to compositional differences in soils above the caves. While these differences appear to exert significant control on local fluid evolution, geochemical and isotopic variations suggest that the controlling processes are regionally extensive. Temporal variations in 87Sr/86Sr values and Mg/Ca ratios of dripwaters from some sites over the 4-yr interval correspond with changes in both aquifer and climatic parameters. These results have important implications for the interpretation of trace element and isotopic variations in speleothems as paleoclimate records, as well as the understanding of controls on water chemistry for both present-day and ancient carbonate aquifers.  相似文献   

19.
《Applied Geochemistry》1998,13(5):593-606
The comparative geochemical and isotopic study of confined and unconfined Chalk groundwaters of the Paris Basin and the N German Basin proves a significant chemical evolution during groundwater flow from the recharge zones to the deep confined aquifer. Different time dependent geochemical parameters have been tested as dating tools: Cation ratios (Sr2+/Ca2+, Mg2+/Ca2+), N–NO−3, noble gas contents as paleotemperature indicators (Ne, Ar, Kr, Xe), radiogenic He, 13C, 14C, 18O, 2H, 3H. Cation ratios and 13C show the importance of incongruent dissolution processes in the Chalk aquifer. Water–rock interactions were taken into account in a multi-step dissolution model to determine radiocarbon groundwater ages. The oldest waters in the confined part of the Paris basin Chalk with maximum 14C ages of 14,000 a B.P. contain pleistocene recharge components as can be shown by a stable isotope depletion and noble gas temperatures significantly lower than in recent groundwaters. Chalk waters at the Lägerdorf site in Northern Germany show a distinct stratification with respect to residence times and hydrochemistry.  相似文献   

20.
Groundwater resources in the North China Plain (NCP) are undergoing tremendous changes in response to the operation of groundwater exploitation reduction (GWER) project. To identify groundwater evolution in this complex context, hierarchical cluster analysis (HCA) and principal component analysis (PCA) were combined to interpret an integrated dataset of stable isotopes and chemical data from four sampling campaigns in a pilot area of groundwater control. We proposed a novel HCA approach integrating stable isotopes and chemical signals, which successfully partitioned the groundwater samples into the unconfined and the confined water samples. Stable isotopic evidence showed that the lateral inflow and the surface water may contribute more to groundwater recharge in this region than local modern precipitation. The unconfined water’s main hydrochemical types were Na type with mixed anions, and Na–Cl–SO4 type, while the confined water was mainly Na–Cl and Na–SO4 types. Geochemical processes mainly involved the dissolution/precipitation of halite, gypsum, Glauber's salt, feldspar, calcite and dolomite, as well as the cation exchange. PCA results showed that water–rock interaction (i.e., salinity-based and alkalinity-based processes) predominated the hydrochemical evolution, along with local nitrate contamination resulting from fertilizers and domestic sewage. The GWER project regulated the natural evolution of unconfined water chemistry, and significantly reduced the unconfined water’s salinity (mainly Na+, Mg2+, SO42?). This may be attributed to upward leakage from low-salinity confined water at some parts of the aquifer. Additionally, insignificant changes in the confined water’s salinity reflected that the impact of GWER on the confined aquifer was negligible. This study facilitates the groundwater classification effectively in the areas lack of geological data, and enhances the knowledge of groundwater chemical evolution in such a region where groundwater restoration is in progress, with important implications for groundwater sustainable management in similar basins worldwide.  相似文献   

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