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1.
ABSTRACT

Hydrogeochemical investigations were carried out with an objective to identify the processes affecting the chemistry of groundwater in the Coimbatore district of Tamil Nadu, India. Thirty-three groundwater samples were collected from representative wells for chemical analysis. Groundwater types identified from piper plots were Ca-Mg-Cl and Na-Cl. The dominance of ions was in the order of Na>Ca>Mg>K and Cl>HCO3>SO4>CO3. Spatial variation diagrams of ions were generated using the geostatistical analyst tool ArcGIS 9.3. According to these diagrams, most of the ions were higher in the northeast and southeast regions. This is attributed to the flow direction of the groundwater and high residence times. Gibbs diagrams identified rock–water interaction as an important geochemical process in the district. Evaporation, ion exchange, silicate weathering and dissolution of carbonate minerals were identified as other important hydrogeochemical processes which influence the groundwater chemistry of the study area.
EDITOR D. Koutsoyiannis ASSOCIATE EDITOR M. Besbes  相似文献   

2.
In the Manas River basin (MRB), groundwater salinization has become a major concern, impeding groundwater use considerably. Isotopic and hydrogeochemical characteristics of 73 groundwater and 11 surface water samples from the basin were analysed to determine the salinization process and potential sources of salinity. Groundwater salinity ranged from 0.2 to 11.91 g/L, and high salinities were generally located in the discharge area, arable land irrigated by groundwater, and depression cone area. The quantitative contributions of the evaporation effect were calculated, and the various groundwater contributions of transpiration, mineral dissolution, and agricultural irrigation were identified using hydrogeochemical diagrams and δD and δ18O compositions of the groundwater and surface water samples. The average evaporation contribution ratios to salinity were 5.87% and 32.7% in groundwater and surface water, respectively. From the piedmont plain to the desert plain, the average groundwater loss by evaporation increased from 7% to 29%. However, the increases in salinity by evaporation were small according to the deuterium excess signals. Mineral dissolution, transpiration, and agricultural irrigation activities were the major causes of groundwater salinization. Isotopic information revealed that river leakage quickly infiltrated into aquifers in the piedmont area with weak evaporation effects. The recharge water interacted with the sediments and dissolved minerals and subsequently increased the salinity along the flow path. In the irrigation land, shallow groundwater salinity and Cl? concentrations increased but not δ18O, suggesting that both the leaching of soil salts due to irrigation and transpiration effect dominated in controlling the hydrogeochemistry. Depleted δ18O and high Cl? concentrations in the middle and deep groundwater revealed the combined effects of mixing with paleo‐water and mineral dissolution with a long residence time. These results could contribute to the management of groundwater sources and future utilization programs in the MRB and similar areas.  相似文献   

3.
Groundwater resources in Mahdia-Ksour Essef region, located in the central-eastern part of Tunisia, suffer from intensive exploitation and degradation of water quality. The assessment of groundwater vulnerability, the well-understanding of geochemical processes and the investigation of groundwater quality variations are of particular importance for water resources management in this semi-arid region. The results of this multi-disciplinary investigation show that groundwaters of Mahdia-Ksour Essef region are flowing from El Jem and Boumerdes regions in the South, towards the Mediterranean Sea and the sebkha of Moknine in the North. The groundwaters are classified as either Na-Cl or Ca-SO4. Stable oxygen and hydrogen isotope compositions (δ18O and δ2H) confirm a recharge by rapid water infiltration, evaporate surface water and water-rock interaction processes in the salinity increase. The rock-water interaction processes of the mineralization of groundwaters include the cation-exchange reactions and the dissolution of carbonates and evaporate. The high values of the water quality index (WQI) and of the total dissolved solids (TDS) (3.7–11 g/L) of these groundwaters indicate their unsuitability for drinking purpose. Moreover, the combination of the WQI, TDS and nitrate results prove the vulnerability of the studied groundwater to the anthropogenic pollution linked to agriculture and domestic activities and to the salt water contamination.  相似文献   

4.
The mean residence time (MRT) of karst groundwater in three mountainous catchments of the Western Himalaya was estimated using multiple approaches: the tritium method, the sine wave model and tracer tests. Water samples were collected from precipitation, glacier melt, streams and karst springs for δ2H and tritium analysis during 2012 and 2013. High tritium values were observed in winter precipitation and low values in summer precipitation. The variation of tritium in karst springs was similar to that of the streams, whereas glacier melt showed lower tritium values. The MRT of cold karst springs was shorter than that of warm karst springs. The tracer breakthrough curves (TBC) retrieved for different springs suggested a short travel time for groundwater and possibly conduit flow. Deterioration of water quality and variation in flux magnitude are the two main practical consequences of the short travel time of karst groundwater in the region.
EDITOR D. Koutsoyiannis

ASSOCIATE EDITOR K. Heal  相似文献   

5.
The impacts of long-term pumping on groundwater chemistry remain unclear in the Manas River Basin, Northwest China. In this study, major ions within five surface water and 105 groundwater samples were analyzed to identify hydrogeochemical processes affecting groundwater composition and evolution along the regional-scale groundwater flow paths using the multivariate techniques of hierarchical cluster analysis (HCA) and principal components analysis (PCA) and traditional graphical methods for analyzing groundwater geochemistry. HCA classified the groundwater samples into four clusters (C1 to C4). PCA reduced the dimensionality of geochemical data into three PCs, which explained 86% of the total variance. The results of HCA and PCA were used to identify three zones: “recharge,” “transition,” and “discharge.” In the recharge zone the groundwater type is Ca-HCO3-SO4 and is primarily impacted by the dissolution of calcite and silicate weathering. In the transition zone the groundwater type is Ca-HCO3-SO4-Cl and is impacted by rock dissolution and reverse ion exchange. In the discharge zone the groundwater type is Na-Cl and is impacted by evaporation and reverse ion exchange. In addition, anthropogenic activities impact the groundwater chemistry in the study area. The groundwater type generally changes from Ca-HCO3-SO4 in the recharge area to Na-Cl in the discharge area along the regional-scale groundwater flow paths. This study provides a process-based knowledge for understanding the interaction of groundwater flow patterns and geochemical evolution within the Manas River Basin.  相似文献   

6.
Groundwater samples were collected from 11 springs in Ash Meadows National Wildlife Refuge in southern Nevada and seven springs from Death Valley National Park in eastern California. Concentrations of the major cations (Ca, Mg, Na and K) and 45 trace elements were determined in these groundwater samples. The resultant data were subjected to evaluation via the multivariate statistical technique principal components analysis (PCA), to investigate the chemical relationships between the Ash Meadows and Death Valley spring waters, to evaluate whether the results of the PCA support those of previous hydrogeological and isotopic studies and to determine if PCA can be used to help delineate potential groundwater flow patterns based on the chemical compositions of groundwaters. The results of the PCA indicated that groundwaters from the regional Paleozoic carbonate aquifers (all of the Ash Meadows springs and four springs from the Furnace Creek region of Death Valley) exhibited strong statistical associations, whereas other Death Valley groundwaters were chemically different. The results of the PCA support earlier studies, where potentiometric head levels, δ18O and δD, geological relationships and rare earth element data were used to evaluate groundwater flow, which suggest groundwater flows from Ash Meadows to the Furnace Creek springs in Death Valley. The PCA suggests that Furnace Creek groundwaters are moderately concentrated Ash Meadows groundwater, reflecting longer aquifer residence times for the Furnace Creek groundwaters. Moreover, PCA indicates that groundwater may flow from springs in the region surrounding Scotty's Castle in Death Valley National Park, to a spring discharging on the valley floor. The study indicates that PCA may provide rapid and relatively cost‐effective methods to assess possible groundwater flow regimes in systems that have not been previously investigated. Copyright © 1999 John Wiley & Sons, Ltd.  相似文献   

7.
ABSTRACT

Five-year monitoring of physicochemical parameters was performed with two campaigns in low and high water periods of the Lower Soummam catchment. Data from 18 wells were processed by multivariate statistical tools in order to identify the principal factors influencing groundwater chemistry. Two matrices of 14 and 8 physicochemical parameters with 18 groundwater samples collected in wells were obtained. The correlation matrix showed strong associations between nine variables: K+, Ca2+, Na+, SO42?, Cl?, Mg2+, NO2?, Zn2+ and Sr2+. Principal component analysis and factor analysis showed that the cumulated variance of high and low water periods was of 83.19% and 78.55%, respectively. The variables assigned to the mineralization effect or to pollution indicators were presented by the factor analysis. The bivariate plots confirmed a mineralization model, ascribed to dissolution of geological materials, and to high levels of saline contamination attributed to leakages from sanitary systems. They also showed an increase “upstream to downstream” of the mineralization, visualization of temporal variations, and a dilution process identification of the natural mineralization during the recharge of the aquifer.
EDITOR D. Koutsoyiannis; ASSOCIATE EDITOR X. Chen  相似文献   

8.
Saline seepage zone development, and hence the onset of dryland salinity, is a major environmental problem occurring within the Spicers Creek catchment. The primary objective of this paper was to identify previously unmapped faults and show the correlation between these faults and groundwater salinization. As identified from this study, there is a close association between geological structural features and the formation of saline seepage zones. The most saline groundwaters in the catchment were encountered where two geological structures join and form a fault intersection. These saline groundwaters are found at various depths within the fractured aquifers, and changes in groundwater chemistry in the aquifers are associated with the presence of fault zones. 18O and δ2H stable isotopes, together with 87Sr/86Sr isotopic ratios, indicate that groundwaters within the fault zones are enriched in 18O and have a strontium signature similar to seawater. This study identifies several geological structures in the Spicers Creek catchment and demonstrates that groundwaters with the highest salinity arise where fault intersections occur. The results of this study may be used to interpret further the mechanisms leading to seepage zone formation in dryland salinity‐affected catchments located throughout the Central West region of New South Wales, Australia. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

9.
In the arid to semi-arid district of Chengcheng, Weinan City, in central Shaanxi Province, diminishing groundwater reserves in the shallow Quaternary (QLB) aquifer and elevated fluoride in the similarly shallow Permo-Triassic (PTF) aquifer, have promoted interest in the development of groundwater resources in the deep but poorly understood Cambrian-Ordovician carbonate aquifer system (COC). To investigate the origin of the COC groundwaters and the relationship between the deep and shallower systems, a hydrochemical study was undertaken involving 179 major and minor ion analyses, 39 stable isotope analyses (δD and δ18O), and 14 carbon isotope analyses (14C and δ13C). PHREEQC 3.0 was used to investigate mixing. Hydrochemical data support the presence of a well-connected regional flow system extending southwards from the more mountainous north. Stable isotope data indicate that the COC groundwaters originate as soil zone infiltration, under a much cooler regime than is found locally today. This is confirmed by 14C, which indicates the groundwater to be palaeowater recharged during the late Pleistocene (∼10–12 ka B.P.). The presence of nitrate in the COC groundwaters suggests leakage from overlying shallow aquifers currently provides an additional source of COC recharge, with major faults possibly providing the primary pathways for downward vertical flow.  相似文献   

10.
The groundwater of the Korba plain represents major water resources in Tunisia. The Plio‐Quaternary unconfined aquifer of the Cap‐Bon (north‐east Tunisia) is subject to the intensive agricultural activities and high groundwater pumping rates due to the increasing of the groundwater extraction. The degradation of the groundwater quality is characterized by the salinization phenomena. Groundwater were sampled and analysed for physic‐chemical parameters: Ca2+, Mg2+, Na+, K+, Cl, SO42‐, HCO3, NO3, pH, electrical conductivity (EC), and the temperature (T°). The hydrochemical analysis is coupled with the calculation of the saturation indexes (SI gypsum, SI halite, SI calcite and SI dolomite), ionic derivation and with the ion correlations compared to chloride concentrations: Na+/ Cl, Ca2+/ Cl and Mg2+/ Cl ratios. Seawater fractions in the groundwater were calculated using the chloride concentration. Those processes can be used as indicators of seawater intrusion progression. EC methods were also conducted to obtain new informations on the spatial scales and dynamics of the fresh water–seawater interface of coastal groundwater exchange. The mixing zone between freshwater and saltwater was clearly observed from the EC profile in the investigated area where a strong increase in EC with depth was observed, corresponding to the freshwater and saltwater interface. Results of hydrochemical study revealed the presence of direct cation exchange linked to seawater intrusion and dissolution processes associated with cations exchange. These results, together with EC investigation, indicated that the groundwater is affected by seawater intrusion and is still major actor as a source of salinization of the groundwater in Korba coastal plain. Further isotopic and hydrological investigations will be necessary to identify and more understood the underlying mechanisms. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

11.
Abstract

The Complex Terminal (CT) and Plio-Quaternary (P-Q) aquifers in the Chott Gharsa plain in southwestern Tunisia have been investigated with the aid of chemical and isotopic tools. It has been demonstrated that groundwater from the CT is mainly of palaeo-origin, especially in the western and central parts of the plain where the most negative values of δ18O and δ2H were observed (between??8.1 and??7.6‰ for δ18O, and??60 to??57‰ for δ2H), combined with low concentrations of radiocarbon (6.8–7.5 pmc) and absence of tritium. Modern recharge of the aquifer occurs only in the eastern part of the system where younger waters were observed, as indicated by their stable isotope composition, relatively high radiocarbon content and presence of tritium. Groundwater from the P-Q multi-layer aquifer represents mixtures of ascending deep CT waters and modern water recharging the P-Q aquifer system. Isotope mass balance was used to quantify mixing proportions. The calculations showed that the contribution of deep CT groundwater to the P-Q aquifer system reaches about 75% in the western and central parts of the plain where the CT aquifer remains strongly artesian. This contribution decreases to about 15% towards the eastern part of the plain, as a consequence of significant reduction of artesian pressure in this area of the CT aquifer. Chemical data suggest that mineralization of the studied groundwater systems is controlled mainly by dissolution of evaporative minerals (halite, anhydrite and gypsum) and cation exchange reactions with the matrix, possibly enhanced by recent anthropogenic disturbance of the system caused by lowering of the water table due to heavy exploitation and return flow of saline irrigation water into the P-Q aquifer.

Editor D. Koutsoyiannis; Associate editor E. Custodio

Citation Yangui, H., Abidi, I., Zouari, K., and Rozanski, K., 2012. Deciphering groundwater flow between the Complex Terminal and Plio-Quaternary aquifers in Chott Gharsa plain (southwestern Tunisia) using isotopic and chemical tools. Hydrological Sciences Journal, 57 (5), 967–984.  相似文献   

12.
We used hydrochemistry and environmental isotope data (δ18O, δD, tritium, and 14C) to investigate the characteristics of river water, groundwater, and groundwater recharge in China's Heihe River basin. The river water and groundwater could be characterized as Ca2+? Mg2+? HCO3?? SO42? and Na+? Mg2+? SO42?? Cl? types, respectively. Hydrogeochemical modelling using PHREEQC software revealed that the main hydrogeochemical processes are dissolution (except for gypsum and anhydrite) along groundwater flow paths from the upper to middle Heihe reaches. Towards the lower reaches, dolomite and calcite tend to precipitate. The isotopic data for most of the river water and groundwater lie on the global meteoric water line (GMWL) or between the GMWL and the meteoric water line in northwestern China, indicating weak evaporation. No direct relationship existed between recharge and discharge of groundwater in the middle and lower reaches based on the isotope ratios, d‐excess, and 14C values. On the basis of tritium in precipitation and by adopting an exponential piston‐flow model, we evaluated the mean residence time of shallow groundwater with high tritium activities, which was around 50 years (a). Furthermore, based on the several popular models, it is calculated that the deep groundwaters in piedmont alluvial fan zone of the middle reaches and in southern part of the lower reaches are modern water, whereas the deep groundwaters in the edge of the middle reaches and around Juyan Lake in the lower reaches of Heihe river basin are old water. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

13.
ABSTRACT

Groundwater is used by 3?million inhabitants in the coastal urban city of Douala, Cameroon, but comprehensive data are too sparse for it to be managed in a sustainable manner. Hence this study aimed to (1) assess the potability of the groundwater; (2) evaluate the spatial variation of groundwater composition; and (3) assess the interaction and recharge mechanisms of different water bodies. Hydrogeochemical tools and methods revealed the following results in the Wouri and Nkappa formations of the Douala basin, which is beneath Douala city: 30% of water samples from hand-dug wells in the shallow Pleistocene alluvium aquifer were saline and highly mineralized. However, water from boreholes in the deeper (49–92 m depth) Palaeocene aquifer was saline-free, less mineralized and potable. Water in the shallow aquifer (0.5–22 m depth) was of Na+-K+-Cl?-NO3? type and not potable due to point source pollution, whereas Ca+-HCO3? unpolluted water dominates in the deeper aquifer. Water in the deep and shallow aquifers indicates the results of preferential flow pass and evaporative recharge, respectively. Possible hydrogeochemical processes include point source pollution, reverse ion exchange, remote recharge areas and mixing of waters with different chemical signatures.
EDITOR D. Koutsoyiannis ASSOCIATE EDITOR M.D. Fidelibus  相似文献   

14.
Abstract

In order to evaluate groundwater quality and geochemical reactions arising from mixing between seawater and dilute groundwater, we performed a hydrochemical investigation of alluvial groundwater in a limestone-rich coastal area of eastern South Korea. Two sites were chosen for comparison: an upstream site and a downstream site. Data of major ion chemistry and ratios of oxygen–hydrogen isotopes (δ18O, δD) revealed different major sources of groundwater salinity: recharge by sea-spray-affected precipitation in the upstream site, and seawater intrusion and diffusion zone fluctuation in the downstream site. The results of geochemical modelling showed that Ca2+ enrichment in the downstream area is caused by calcite dissolution enhanced by the ionic strength increase, as a result of seawater–groundwater mixing under open system conditions with a constant PCO2 value (about 10?1.5 atm). The results show that, for coastal alluvial groundwater residing on limestone, significant hydrochemical change (especially increased hardness) due to calcite dissolution enhanced by seawater mixing should be taken into account for better groundwater management. This process can be effectively evaluated using geochemical modelling.

Editor D. Koutsoyiannis; Associate editor Y. Guttman

Citation Chae, G.-T., Yun, S.-T., Yun, S.-M., Kim, K.-H., and So, C.-S., 2012. Seawater–freshwater mixing and resulting calcite dissolution: an example from a coastal alluvial aquifer in eastern South Korea. Hydrological Sciences Journal, 57 (8),1–12.  相似文献   

15.
The origin and the chemical and isotopic evolution of dissolved inorganic carbon (DIC) in groundwater of the Okavango Delta in semi-arid Botswana were investigated using DIC and major ion concentrations and stable oxygen, hydrogen and carbon isotopes (δD, δ18O and δ13CDIC). The δD and δ18O indicated that groundwater was recharged by evaporated river water and unevaporated rain. The river water and shallow (<10 m) groundwater are Ca–Na–HCO3 type and the deep (≥10 m) groundwater is Na–K–HCO3 to HCO3–Cl–SO4 to Cl–SO4–HCO3. Compared to river water, the mean DIC concentrations were 2 times higher in shallow groundwater, 7 times higher in deep groundwater and 24 times higher in island groundwater. The δ13CDIC indicate that DIC production in groundwater is from organic matter oxidation and in island groundwater from organic matter oxidation and dissolution of sodium carbonate salts. The ionic and isotopic evolution of the groundwater relative to evaporated river water indicates two independent pools of DIC.  相似文献   

16.
High groundwater salinity has become a major concern in the arid alluvial plain of the Dunhuang Basin in northwestern China because it poses a significant challenge to water resource management. Isotopic and geochemical analyses were conducted on 55 water samples from springs, boreholes and surface water to identify potential sources of groundwater salinity and analyse the processes that control increasing salinity. The total dissolved solid (TDS) content in the groundwater ranged from 400 to 41 000 mg/l, and high TDS values were commonly associated with shallow water tables and flow‐through and discharge zones in unconfined aquifers. Various groundwater contributions from rainwater, agricultural irrigation, river water infiltration and lateral inflows from mountains were identified by major ions and δD and δ18O. In general, HCO3? and SO42? were the dominant anions in groundwater with a salinity of <2500 mg/l, whereas Cl? and SO42? were the dominant anions in groundwater with a salinity of >2500 mg/l. The major ion concentrations indicated that mineral weathering, including carbonate and evaporite dissolution, primarily affected groundwater salinity in recharge areas. Evapotranspiration controlled the major ion concentration evolution and salinity distribution in the unconfined groundwaters in the flow‐through and discharge areas, although it had a limited effect on groundwater in the recharge areas and confined aquifers. Agricultural irrigation increased the water table and enhanced evapotranspiration in the oasis areas of the basin. TDS and Cl became more concentrated, but H and O isotopes were not enriched in the irrigation district, indicating that transpiration dominated the increasing salinity. For other places in the basin, as indicated by TDS, Cl, δD and δ18O characteristics, evaporation, transpiration and water–rock interactions dominated at different hydrogeological zones, depending on the plant coverage and hydrogeological conditions. Groundwater ages of 3H, and δD and δ18O compositions and distributions suggest that most of the groundwaters in Dunhuang Basin have a paleometeoric origin and experienced a long residence time. These results can contribute to groundwater management and future water allocation programmes in the Dunhuang Basin. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

17.
《水文科学杂志》2013,58(4):781-792
Abstract

Groundwaters of known age contained in major aquifer systems in the African sedimentary basins enable low-resolution (±1000 year) characteristics of past climates to be determined, specifically palaeo-temperature, air mass origins, humid/arid transitions and rainfall intensity. Results from both northern and southern Africa indicate the predominance of a westerly Atlantic air flow during the Late Pleistocene. Greater aridity during the Last Glacial Maximum (LGM) is recorded over most of northern Africa by the absence of dated groundwaters. An intensification of the African monsoon during the Early Holocene is apparent from isotopically light groundwaters found, in particular, over Sudan. Maximum cooling around the LGM of 5–7°C is recorded in the noble gas recharge temperatures from Africa. Modern recharge can be readily identified from the chemical and isotopic signatures (Cl, δ18O and 3H) in the unsaturated zone and in shallow groundwaters. The results indicate the non-renewability of many groundwater sources now being exploited across the arid and semi-arid regions of Africa. Extreme events in the past, noted from the groundwater record, may have lessons and implications for adapting to future climate change. Small but finite amounts of renewable groundwater may be estimated using chloride mass balance and other tracer techniques. These renewable waters form the basis of sustainable development in areas such as the Sahel. Based on the field evidence of water scarcity, new approaches are needed in management and education to adapt to the current limited resources in the face of changing climates.  相似文献   

18.
The isotopic chemistry of alluvial groundwaters from two adjacent valleys are described and hydrological processes within related aquifers are identified as evidenced by oxygen-18, deuterium, tritium and chloride data. A plot of δ18O against δD values reveals isotopic enrichment of the groundwater by the recycling of spray irrigation water. A plot of tritium versus chloride concentrations displays separate linear correlations for alluvial groundwaters within the two valleys. The salinity has a common source, therefore the separate correlations are interpreted as the past transfer of low salinity groundwater from the alluvial aquifers in one valley to the underlying sandstone aquifers.  相似文献   

19.
Stable isotopes, 2Hwater, 18Owater as well as 18Osulphate and 34Ssulphate, were used to study the flow system of shallow groundwater and soil water at the base area of a former leaching heap at the uranium mining area of Ronneburg, Germany. The flow paths and water‐retention times were estimated by comparison of δ2H and δ18O values in groundwater and soil water to the δ2H and δ18O signature of precipitation, giving distinctive inputs of summer or winter precipitation. The points of measuring the groundwater were divided into three categories with different flow conditions: rapid flow, stagnant conditions and a transition zone by hierarchical cluster analysis of δ2H and δ18O values of groundwater. The transit time of groundwater in the rapid flow area is less than 6 months, whereas water in the stagnant zone is stored for at least 1 year. In soil water, a clear response to different input signals is detectable only in the 30‐cm horizon (retention time is about 6 months), whereas at deeper levels a mixing with older water is taking place. The isotopic composition of the dissolved sulphate was used to identify oxidation of sulphides as the source of sulphate. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

20.
ABSTRACT

Multivariate statistical analysis and inverse geochemical modelling techniques were employed to deduce the mechanism of groundwater evolution in the hard-rock terrain of Telangana, South India. Q-mode hierarchical cluster analysis (HCA) and principal component analysis (PCA) were used to extract the hydrogeochemical characteristics and classify the groundwater samples into three principal groups. Use of thermodynamic stability diagrams and inverse geochemical modelling in PHREEQC identified the chemical reactions controlling hydrogeochemistry of each of the groups obtained from statistical analysis. The model output showed that a few phases are governing the water chemistry in this area and the geochemical reactions responsible for evolution of groundwater chemistry along the flow path are (i) dissolution of evaporite minerals (dolomite, halite); (ii) dissolution of primary silicate minerals (albite, anorthite, K-feldspar, biotite); (iii) precipitation of secondary silicate minerals (kaolinite, quartz, gibbsite, Ca-montmorillonite) along with anhydrite and calcite; and (iv) reverse ion exchange processes.  相似文献   

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