首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
A comprehensive and systematic study to understand various geochemical processes as well as process drivers controlling the water quality and patterns of the hydrochemical composition of river water in Muthirapuzha River Basin, MRB (a major tributary of Periyar, the longest river in Kerala, India), was carried out during various seasons, such as monsoon, post-monsoon and pre-monsoon of 2007–2008, based on the data collected at 15 monitoring stations (i.e., 15 × 3 = 45 samples). Ca2+ and Mg2+ dominate the cations, while Cl? followed by HCO3 ? dominates the anions. In general, major ion chemistry of MRB is jointly controlled by weathering of silicate and carbonate rocks, which is confirmed by relatively larger Ca2+ + Mg2+/Na+ + K+ ratios as well as Ca2+/Na+ vs. Mg2+/Na+ and Ca2+/Na+ vs. HCO3 ?/Na+ scatter plots. The relationship between Cl? and Na+ implies stronger contributions of anthropogenic activities modifying the hydrochemical composition, irrespective of seasons. The water types emerged from this study are transitional waters or waters that changed their chemical character by mixing with waters of geochemically different ionic signatures. However, various ionic ratios, hydrochemical plots and graphical diagrams suggest seasonality over the hydrochemical composition, which is solely controlled by the rainfall pattern. Relatively higher pCO2 indicates the disequilibrium existing in natural waterbodies vis-à-vis the atmosphere, which is an outcome of both the contribution of groundwater to stream discharge and anthropogenic activities. Hence, continuous monitoring of hydrochemical composition of mountain rivers is essential in the context of climate change, which has serious implications on tropical mountain fluvial-hydro systems.  相似文献   

2.
The assessment of hydrogeochemical processes that govern the water quality of inland freshwater aquifers in coastal environment, especially in Indian sub-continent, is occasionally attempted. To bridge the gap, a detail hydrochemical evaluation of groundwater occurring in coastal alluvium is attempted. Single set of high-density water sampling is done from a limited area to gain an in-depth knowledge of the processes that govern the water chemistry of the sandy aquifers. The water is of weak alkaline nature and less mineralized, EC being < 1,000 μS/cm in many samples. Major ion composition indicates that water is contaminated with excess concentration of nitrates. Ionic abundance is in the order of Cl? > Na+  > Ca2+ > HCO3 ? > SO4 2? > Mg2+  > NO3 ?. Na+ and Cl? are almost in similar proportions implying the influence of coastal climate on water quality. The water shows modest variation in their ionic assemblage among different sample points as evident from Schoeller scheme. Groundwater can be classified into three distinct facies viz. Cl?–Ca2+–Mg2+, Na+–Cl? and Ca2+–Mg2+–HCO3 ? types. The ionic assemblages, their indices, ratios and cross-plots substantiate that multiple processes were involved in the evolution of the water chemistry. Among them, silicate weathering, halite dissolution, ion exchange and base exchange played prominent role in the ion enrichment of groundwater. The aquatic chemistry is further influenced and modified by marine environment, evapotranspiration and anthropogenic inputs which is authenticated by good correlation (r 2 = 1) among the Na+–Cl?, EC–Mg2+, Na+ and Cl?. Gibbs plots established that evaporation is more responsible for contribution of minerals to the groundwater than aquifer material. Nitrate contamination can be attributed for poor sewerage disposal mechanism which is aggravated by fertilizer inputs, irrigation practices and agriculture activity. A contrasting correlation (r 2 ≥90 to <0.40) among select pairs of ions reassures dissimilar source of those ions, involvement of multiple processes and limited interaction of formation water with aquifer material.  相似文献   

3.
Based on analysis of groundwater hydrogeochemical and isotopic data, this study aims to identify the recharge sources and understand geochemical evolution of groundwater along the downstream section of the Shule River, northwest China, including two sub-basins. Groundwater samples from the Tashi sub-basin show markedly depleted stable isotopes compared to those in the Guazhou sub-basin. This difference suggests that groundwater in the Tashi sub-basin mainly originates from meltwater in the Qilian Mountains, while the groundwater in the Guazhou sub-basin may be recharged by seepage of the Shule River water. During the groundwater flow process in the Tashi sub-basin, minerals within the aquifer material (e.g., halite, calcite, dolomite, gypsum) dissolve in groundwater. Mineral dissolution leads to strongly linear relationships between Na+ and Cl? and between Mg2++ Ca2+ and SO4 2??+?HCO3 ?, with stoichiometry ratios of approximately 1:1 in both cases. The ion-exchange reaction plays a dominant role in hydrogeochemical evolution of groundwater in the Guazhou sub-basin and causes a good linear relationship between (Mg2++ Ca2+)–(SO4 2??+?HCO3 ?) and (Na++ K+)–Cl? with a slope of ?0.89 and also results in positive chloroalkaline indices CAI 1 and CAI 2. The scientific results have implications for groundwater management in the downstream section of Shule River. As an important irrigation district in Hexi Corridor, groundwater in the Guazhou sub-basin should be used sustainably and rationally because its recharge source is not as abundant as expected. It is recommended that the surface water should be used efficiently and routinely, while groundwater exploitation should be limited as much as possible.  相似文献   

4.
The Densu River Basin (DRB) is an important agricultural area in Ghana and has a high population density. Water shortages have occurred in the basin due to drying out of surface water, heavy pollution and low yield in most of the production wells, which are crucial factors restricting sustainable socioeconomic development. This study was carried out to investigate the geochemical characteristics and evolution, as well as recharge processes in the DRB system with regard to the tectonics, geomorphology, lithology and flow system. It mainly used hydrochemistry, environmental isotopes and a series of comprehensive data interpretation, e.g., statistics, ionic ratios and Piper diagram to obtain a better understanding of the functioning of the system. The following hydrochemical processes were identified as the main factors controlling the water quality of the groundwater system: weathering of silicate minerals, dissolution, ion exchange and, to a lesser extent, evaporation, which seems to be more pronounced downgradient of the flow system. As groundwater flows from the recharge to discharge areas, chemical patterns evolve in the order of Ca2+–HCO3 ?, Ca2+/Mg2+–HCO3 ? to Ca2+/Na+–Cl?, Ca2+–Na+–HCO3 ? and Na+–Cl? according to lithology. The environmental isotope (δ18O, δ2H, 3H) measurements further revealed that groundwater in the DRB was a relatively well-mixed system as evidenced by the encoded narrow range of values. However, deviation from the rainwater signature indicates combined local processes such as direct percolation through preferential channels, evaporation, and probable surface water and anthropogenic contribution to the system.  相似文献   

5.
Hydrogeochemical controlling factors for high rate of groundwater contamination in stressed aquifer of fractured, consolidated rocks belonging to semi-arid watershed are examined. The groundwater in mid-eastern part of Prakasam district confining to Musi-Gundlakamma sub-basins is heavily contaminated with nitrate and fluoride. Distinct water chemistry is noticed among each group of samples segregated based on concentration of these contaminants. The nitrate is as high as 594 mg/l and 57 % of the samples have it in toxic level as per BIS drinking water standards, so also the fluoride which has reached a maximum of 8.96 mq/l and 43 % of samples are not fit for human consumption. Nitrate contamination is high in shallow aquifers and granitic terrains, whereas fluoride is in excess concentration in deeper zones and meta-sediments among the tested wells, and 25 % of samples suffer from both NO3 ? and F? contamination. Na+ among cations and HCO3 ? among anions are the dominant species followed by Mg2+ and Cl?. The NO3 ?-rich groundwater is of Ca2+–Mg2+–HCO3 ?, Ca2+–Mg2+–Cl? and Na+–HCO3 ? type. The F?-rich groundwater is dominantly of Na+–HCO3 ? type and few are of Na+–SO4 2? type, whereas the safe waters (without any contaminants) are of Ca2+–Mg2+–HCO3 ?– and Na+–HCO3 ? types. High molecular percentage of Na+, Cl?, SO4 2? and K? in NO3 ? rich groundwater indicates simultaneous contribution of many elements through domestic sewerage and agriculture activity. It is further confirmed by analogous ratios of commonly associated ions viz NO3 ?:Cl?:SO4 2? and NO3 ?:K+:Cl? which are 22:56:22 and 42:10:48, respectively. The F? rich groundwater is unique by having higher content of Na+ (183 %) and HCO3 ? (28 %) than safe waters. The K+:F?:Ca2+ ratio of 10:5:85 and K+:F?: SO4 2? of 16:7:77 support lithological origin of F? facilitated by precipitation of CaCO3 which removes Ca2+ from solution. The high concentrations of Na+, CO3 ? and HCO3 ? in these waters act as catalyst allowing more fluorite to dissolve into the groundwater. The indices, ratios and scatter plots indicate that the NO3 ? rich groundwater has evolved through silicate weathering-anthropogenic activity-evapotranspiration processes, whereas F? rich groundwater attained its unique chemistry from mineral dissolution-water–rock interaction-ion exchange. Both the waters are subjected to external infusion of certain elements such as Na+, Cl?, NO3 ? which are further aggravated by evaporation processes leading to heavy accumulation of contaminants by raising the water density. Presence of NO3 ? rich samples within F? rich groundwater Group and vice versa authenticates the proposed evolution processes.  相似文献   

6.
Conventional hydrogeochemical data and environmental stable isotopes are used to identify the recharge sources and the water–rock interactions in the groundwater-flowing direction within the multilayer groundwater system of the Sulin coal-mining district in the north Anhui province in China. δD and δ 18O of groundwater in the mining district decrease along the groundwater-flowing direction in the recharge areas, yet in the runoff or discharge areas, they rise and fall along average δ values (δ 18O = ?8.68 ‰, δD = ?67.4 ‰), which are lower than average δ values of local atmospheric precipitation (δ 18O = ?7.80 ‰, δD = ?52.4 ‰). Principal component analysis is used to analyze the conventional hydrogeochemical data (K+ + Na+, Mg2+, Ca2+, Cl?, SO4 2?, HCO3 ?, CO3 2?) in the groundwater. The first and second principal components have large variance contributions, and represent “pyrite oxidation or groundwater hardening” and “desulfurization or cation exchange and adsorption,” respectively. From conventional hydrogeochemical data and environmental stable isotopes, it is demonstrated that groundwater of the Sulin coal-mining district is characterized by a mixing type, which is confirmed by three recharge end-members: fresh groundwater, leaching groundwater, and retained groundwater. By means of a sample dot-encompassed triangle in the scatter diagram of load scores for Component 1–Component 2, whose vertexes stand for the three end-members, a model for calculating groundwater mixing ratio is established and applied successfully to the evaluation and management of groundwater hazards in the coal-mining districts.  相似文献   

7.
As one of the most arid regions in the world, the study area, Zhangye Basin is located in the middle reaches of the Heihe River, northwest China. Besides aridity, rapid social and economic development also stimulates greater demand for water, which is gradually fulfilled by groundwater extraction. In this study, the conventional hydrochemical techniques and statistical analyses were applied to examine the major ions chemistry and hydrochemical processes of groundwater in the Zhangye Basin. The results of chemical analysis indicate that no one pair of cations and anions proportions is more than 50% in the groundwater samples of the study area. High-positive correlations were obtained among the following ions: HCO3 ?–Mg2+, SO4 2?–Mg2+, SO4 2?–Na+ and Cl?–Na+. TDS depends mainly on the concentration of major ions such as HCO3 ?, SO4 2?, Cl?, Mg2+ and Na+. The hydrochemical types in the area can be divided into two major groups: the first group includes Mg2+–Na+–HCO3 ?, Mg2+–Na+–Ca2+–HCO3 ?–SO4 2? and Mg2+–Ca2+–Na+–SO4 2?–HCO3 ? types. The second group comprises Mg2+–Ca2+–SO4 2? type, Mg2+–Ca2+–SO4 2?–Cl? type and Mg2+–Na+–SO4 2?–Cl? type. The ionic ratio plot and saturation index calculation suggests that the silicate weathering, to some extent, and evaporation are dominant factors that determine the major ionic composition in the study area.  相似文献   

8.
Hydrogeochemical investigation of groundwater has been carried out in the coastal aquifers of southern Tamil Nadu, India. Seventy-nine dug well samples were collected and analyzed for various physicochemical parameters. The result of the geochemical analysis indicates the groundwater in the study area is slightly alkaline with moderate saline water. The cation and anion concentrations confirm most of the groundwater samples belong to the order of Na+ > Mg2+ > Ca2+ > K+ and Cl? > SO4 2? > HCO3 ?. Thereby three major hydrochemical facies (Ca–Cl, mixed Ca–Mg–Cl and Na–Cl) were identified. Based on the US Salinity diagram, majority of the samples fall under medium to very high salinity with low to high sodium hazard. The cross plot of Ca2+ + Mg2+ versus chloride shows 61 % of the samples fall under saline water category. Higher EC, TDS and Cl concentrations were observed from Tiruchendur to Koodankulam coastal zone. It indicates that these regions are significantly affected by saltwater contamination due to seawater intrusion, saltpan deposits, and beach placer mining activities.  相似文献   

9.
Groundwater of the unconfined aquifer (1,100 sq. km) of a two-tier coastal aquifer located in the Amol–Ghaemshahr plain, Mazandaran Province, Northern Iran, is classified into fresh and brackish water types. Fresh groundwater (FGW) samples (n = 36) are characterized by Ca2+ > Na+ > Mg2+ > K+ and HCO3 ? > Cl? > SO4 2? > NO3 ?. Spearman’s rank correlation coefficient matrices, factor analysis data, values of the C-ratio (av. = 0.89) and CAI and values of the molar ratios of Ca2+/HCO3 ?, Ca2+/SO4 2?, Mg2+/HCO3 ? and Mg2+/SO4 2? indicate that the ionic load in the FGW is derived essentially from carbonic acid-aided weathering of carbonates and aluminosilicates, saline/sea water trapped in the aquifer sediments (now admixed with the groundwater) and ion exchange reactions. Values of the CAI and Na+/Cl? molar ratio suggest that the part of the Ca2+ (±Mg2+) content in 23 FGW samples is derived from clay minerals of the aquifer matrix, and part of the Na+ content in 20, 12, and 3 FGW samples is derived, respectively, from alkali feldspar weathering, clay minerals of the aquifer matrix and rain water and/or halite. Brackish groundwater (BGW) samples (n = 4) contain Cl? as the dominant anion and their average total ionic concentration (38.65 meq/L) is 1.79 times higher than that of the FGW samples (21.50 meq/L). BGW pockets were generated by non-conservative mixing of FGW with the upconed saline water from the underlying saline groundwater zone of the semi-confined aquifer along bore wells involved in excessive extraction of groundwater from the unconfined aquifer. Groundwater belongs essentially to “high salinity, low sodium” irrigation water class.  相似文献   

10.
Twenty groundwater samples were collected from Enugu metropolis over two seasonal periods in order to characterize the groundwater and to determine its quality for domestic and irrigation purposes. The results show that groundwater of the area is strongly acidic to slightly alkaline in nature and varied from “soft water” to “moderately hard” water type. The major ionic trend is in the order Cl? > Na+ > HCO3 ? > K+ > Mg2+ > Ca2+ > SO4 2?and Mg2+ > Cl? > Na+ > K+ > Ca2+ > HCO 3 ?  > SO4 2? in abundance for dry and rainy seasons, respectively. The results also reveal that there is an increase in trend of the ionic concentrations during the dry season, which arises from weathering of the host rocks and anthropogenic activities. Two hydrochemical facies were identified, namely, Na+ –K+ –Cl? –SO4 2?and Ca2+ –Mg2+ –Cl? –SO4 2? , with Na+ –K+ –Cl? –SO4 2? as the dominant facies for the two seasons. Groundwater quality ranges from “very poor water” to “good water” and “water unsuitable for drinking purposes” to “good water” for the dry season and rainy season investigations, respectively. The groundwater is suitable for irrigation purposes for the two seasons.  相似文献   

11.
Groundwater of an aquifer located in the vicinity of a large coal washery near Zarand City, Iran consists of two hydrochemically differing facies, which have been informally designated as groundwater (A) and groundwater (B). Groundwater (A) is native, brackish in composition and is characterized by Na+ > Mg2+ > Ca2+ > K+ and SO4 2? > HCO3 ? > Cl? > NO3 ?. Spearman’s rank correlation coefficient matrices, factor analysis data, and values of chloro-alkaline indices, C ratio and Na+/Cl? molar ratio indicate that in the groundwater (A), the ionic load of Ca2+, Mg2+, Na+, K+, SO4 2? and HCO3 ? is derived essentially from weathering of both carbonates and aluminosilicates and direct cation and reverse cation–anion exchange reactions. Groundwater (B) is the polluted variant of the groundwater (A), brackish to saline in composition, and unlike the groundwater (A), consists of HCO3 ? as the dominant anion. In comparison with the groundwater (A), the groundwater (B) contains higher concentrations of all ions, and its average ionic load (av. = 59.74 me/L) is 1.43 times higher than that of the groundwater (A) (av. = 41.54 me/L). Additional concentrations of Ca2+, Mg2+, K+, SO4 2?, Cl? and HCO3 ? in the groundwater (B) are provided mainly by downward infiltrating water from the coal washery tailings pond and reverse cation–anion exchange reaction between tailings pond water and exchanger of the aquifer matrix during non-conservative mixing process of groundwater (A) and tailings pond water. Certain additional concentrations of Na+, K+ and NO3 ? in the groundwater (B) are provided by other anthropogenic sources. Quality wise, both groundwaters are marginally suitable for cultivation of salt-tolerant crops only.  相似文献   

12.
Groundwater survey has been carried out in the area of Gummanampadu sub-basin located in Guntur District, Andhra Pradesh, India for assessing the factors that are responsible for changing of groundwater chemistry and consequent deterioration of groundwater quality, where the groundwater is a prime source for drinking and irrigation due to non-availability of surface water in time. The area is underlain by the Archaean Gneissic Complex, over which the Proterozoic Cumbhum rocks occur. The results of the plotting of Ca2+ + Mg2+ versus HCO3 ? + CO3 2?, Ca2+ + Mg2+ versus total cations, Na+ + K+ versus total cations, Cl? + SO4 2? versus Na+ + K+, Na+ versus Cl?, Na+ versus HCO3 ? + CO3 2?, Na+ versus Ca2+ and Na+: Cl? versus EC indicate that the rock–water interaction under alkaline condition is the main mechanism in activating mineral dissociation and dissolution, causing the release of Ca2+, Mg2+, Na+, K+, HCO3 ?, CO3 2?, SO4 2? and F? ions into the groundwater. The ionic relations also suggest that the higher concentrations of Na+ and Cl? ions are the results of ion exchange and evaporation. The influences of anthropogenic sources are the other cause for increasing of Mg2+, Na+, Cl?, SO4 2? and NO3 ? ions. Further, the excess alkaline condition in water accelerates more effective dissolution of F?-bearing minerals. Moreover, the chemical data plotted in the Piper’s, Gibbs’s and Langelier–Ludwig’s diagrams, computed for the chloro-alkaline and saturation indices, and analyzed in the principal component analysis, support the above hypothesis. The groundwater quality is, thus, characterized by Na+ > Ca2+ > Mg2+ > K+: HCO3 ? + CO3 2? > Cl? > SO4 2? > NO3 ? > F? facies. On the other hand, majority of groundwater samples are not suitable for drinking with reference to the concentrations of TDS, TH, Mg2+ and F?, while those are not good for irrigation with respect to USSL’s and Wilcox’s diagrams, residual sodium carbonate, and magnesium hazard, but they are safe for irrigation with respect to permeability index. Thus, the study recommends suitable management measures to improve health conditions as well as to increase agricultural output.  相似文献   

13.
Assessment of groundwater quality in and around Vedaraniyam,South India   总被引：1，自引：1，他引：0  
Groundwater from 47 wells were analyzed on the basis of hydrochemical parameters like pH, electric conductivity, total dissolved solids, Ca2+, Mg2+, Na+, K+, Cl?, CO3 2?, HCO3 ?, NO3 ?, PO4 3? and F? in the Cauvery delta of Vedaraniyam coast. Further, water quality index (WQI), sodium percentage (Na %), sodium absorption ratio, residual sodium carbonate, permeability index and Kelley’s ratio were evaluated to understand the suitability of water for drinking and irrigation purposes. The result shows significant difference in the quality of water along the coastal stretch. The order of dominance of major ions is as follows: Na+ ≥ Mg2+ ≥ Ca2+ ≥ K+ and Cl? ≥ HCO3 ? ≥ CO3 2? ≥ PO4 3? ≥ F?. Na/Cl, Cl/HCO3 ratio and Revelle index confirmed that 60–70 % of the samples were affected by saline water intrusion. WQI showed that 36 % of the samples were good for drinking and the remaining were poor and unsuitable for drinking purpose. The degradation of groundwater quality was found to be mainly due to over-exploitation, brackish aquaculture practice, fertilizer input from agriculture and also due to domestic sewage.  相似文献   

14.
The Ganges River water and riverbank shallow groundwater were studied during a single wet season using the hydrochemical and isotopic composition of its dissolved load. The dissolved concentrations of major ions (Cl?, SO4 2?, NO3 ?, HCO3 ?, Ca2+, Na+, Mg2+, and K+), trace elements (barium (Ba) and strontium (Sr)) and stable isotopes (O and D) were determined on samples collected from the Ganges River and its riverbank shallow aquifers. In the present study, the shallow groundwater differs significantly from the Ganges River water; it shows distinct high concentrations of Ca2+, Mg2+, HCO3 ?, Ba, and Sr due to water–rock interaction and this in particular suggests that the Ganges River may not contribute significantly to the riverbank shallow aquifers during wet season. Besides, the sum of the total cationic charge (∑+, in milliequivalents per liter) in the groundwater shows high values (2.48 to 13.91 meq/L, average 9.12 meq/L), which is much higher than the sum of the cations observed in the Ganges water (1.36 to 3.10 meq/L, average 1.94 meq/L). Finally, the more depleted stable isotopic (δ 18O and δ 2H) compositions of the Ganges River water are in contrast to those of the riverbank aquifer having enriched stable isotopic values during the wet season and the riverbank groundwater thus has a purely local origin from precipitation.  相似文献   

15.
In this study, it is determined physicochemical properties of the groundwater and the spatial variability of physicochemical properties of the groundwater in the Amik plain and as well as assess its suitability for drinking and irrigation. A total 92 groundwater samples were collected from drilled well in June 2012. In addition, the 42 of 92 drilled wells were also sampled in September 2012 to evaluate the changes of groundwater properties. According to t test values, the mean Ca2+, SO4 2?, Mg2+ and TH values in the June period were significantly lower than those of the September period. On the other hand, the mean (CO 3 2?  + HCO3 ?) and RSC and MR values in the June period were significantly higher than those of the September period. The order of relative abundance of major cations in the groundwater (in mg L?1) is in order Na+ > Mg2+ > Ca2+ > K+. The order of the anions abundance (mg L?1) is SO4 2? > Cl? > HCO3 ? > CO3 2? in this research. Log and square-root transformation were carried out for the most of the water properties before the calculation of semivariance. The nugget ratio showed all the variables were strongly spatial dependent except for K+ and Mg2+ and (CO3 2? + HCO3 ?) which showed moderate spatial dependence (ratio ranging from 28 to 49.9 %). Spatial distribution analysis of groundwater quality indicated that The EC, TDS values and Na and Cl? contents which is important water quality parameters increase from northern towards southern. The total hardness values increase also from northwestern towards southwestern.  相似文献   

16.
A total of 194 groundwater samples were collected from wells in hard rock aquifers of the Medak district, South India, to assess the distribution of fluoride in groundwater and to determine whether this chemical constituent was likely to be causing adverse health effects on groundwater user in the region. The study revealed that the fluoride concentration in groundwater ranged between 0.2 and 7.4 mg/L with an average concentration of 2.7 mg/L. About 57% of groundwater tested has fluoride concentrations more than the maximum permissible limit of 1.5 mg/L. The highest concentrations of fluoride were measured in groundwater in the north-eastern part of the Medak region especially in the Siddipeta, Chinnakodur, Nanganoor and Dubhaka regions. The areas are underlain by granites which contain fluoride-bearing minerals like apatite and biotite. Due to water–rock interactions, the fluoride has become enriched in groundwater due to the weathering and leaching of fluoride-bearing minerals. The pH and bicarbonate concentrations of the groundwater are varied from 6.6 to 8.8 and 18 to 527 mg/L, respectively. High fluoride concentration in the groundwater of the study area is observed when pH and the bicarbonate concentration are high. Data plotted in Gibbs diagram show that all groundwater samples fall under rock weathering dominance group with a trend towards the evaporation dominance category. An assessment of the chemical composition of groundwater reveals that most of the groundwater samples have compositions of Ca2+–Mg2+–Cl? > Ca2+–Na+–HCO3 ? > Ca2+–HCO3 ? > Na+–HCO3 ?. This suggests that the characteristics of the groundwater flow regime, long residence time and the extent of groundwater interaction with rocks are the major factors that influence the concentration of fluoride. It is advised not to utilize the groundwater for drinking purpose in the areas delineated, and they should depend on alternate safe source.  相似文献   

17.
Quality assessment as well as hydrogeochemical characterization of 45 representative groundwater samples around Umrer coal mine area was undertaken. The pH of the water lies in the normal range i.e. from 7.5 to 8.5, the electrical conductivity varies from 826 to 1,741, the total hardness varies from 289 to 1,302 and the TDS values range from 528.6 to 1,114.2 mg/l which reflects variation in lithology and thus, the distinction in hydrogeological regime. The cation chemistry is dominated by Ca2+ and Mg2+ while anion chemistry is dominated by Cl? and HCO3 ?. Out of total ten hydrochemical facies, the two dominant facies are Mg–Ca–HCO3 (37.7 %) and Ca–Mg–SO4–HCO3 (17.7 %). The groundwater in the study area, in general, is useful for drinking and domestic use; however, it has marginal utility for irrigation purpose. Standard US Salinity Laboratory classification shows that water of the study area belongs to C2–S1 and C3–S1 classes. The concentration of 9 trace elements analysed from 18 samples did not exceed the desirable limit.  相似文献   

18.
Hydrogeochemistry of groundwater is important for sustainable development and effective management of the groundwater resource. Fifty-six groundwater samples were collected from shallow tube wells of the intensively cultivated southern part of district Bathinda of Punjab, India, during pre- and post-monsoon seasons. Conventional graphical plots were used to define the geochemical evaluation of aquifer system based on the ionic constituents, water types, hydrochemical facies and factors controlling groundwater quality. Negative values of chloroalkaline indices suggest the prevalence of reverse ion exchange process irrespective of the seasons. A significant effect of monsoon is observed in terms chemical facies as a considerable amount of area with temporary hardness of Ca2+–Mg2+–HCO3 ? type in the pre-monsoon switched to Ca2+–Mg2+–Cl? type (18%) followed by Na+–HCO3 ? type (14%) in the post-monsoon. Evaporation is the major geochemical process controlling the chemistry of groundwater process in pre-monsoon; however, in post-monsoon ion exchange reaction dominates over evaporation. Carbonate weathering is the major hydrogeochemical process operating in this part of the district, irrespective of the season. The abundance of Ca2+ + Mg2+ in groundwater of Bathinda can be attributed mainly to gypsum and carbonate weathering. Silicate weathering also occurs in a few samples in the post-monsoon in addition to the carbonate dissolution. Water chemistry is deteriorated by land-use activities, especially irrigation return flow and synthetic fertilisers (urea, gypsum, etc.) as indicted by concentrations of nitrate, sulphate and chlorides. Overall, results indicate that different natural hydrogeochemical processes such as simple dissolution, mixing, weathering of carbonate minerals locally known as ‘‘kankar’’ and silicate weathering are the key factors in both seasons.  相似文献   

19.
The physicochemical properties and major ion chemistry of the groundwater sources from alluvial aquifers along the stretch (60 km) of Jhelum River in Kashmir Himalaya were determined in order to identify hydro-geochemical processes and their suitability for drinking purposes. The data depicted that calcium and bicarbonates were dominating among the cations and anions. The results indicate the trend of cation dominance as Ca2+ > Na+ > Mg2+ > K+, whereas anion dominance was in the order of HCO3 ? > Cl? > SO4 2?. Ratio of calcium to magnesium indicated the dissolution of Ca2+ from CaCO3, which results in an increased levels of Ca2+ in the groundwater. Interpretation of Piper Trilinear plot understands the various geochemical processes affecting the groundwater quality and shows groundwater was dominated by Ca–HCO3 type. The pH was recorded in the slightly alkalinity range 7.2–7.8 and was showing positive correlation with HCO3 ?. The chloro-alkaline indices revealed 86% of the sources exchange by a type of base-exchange reactions, rest by cation–anion exchange. Gibbs diagram revealed groundwater sources fall in the category of rock dominance. The concentration of the nitrogen compounds was in the progression of NO3–N > NH4–N > NO2–N, and the PO4 ? fluctuated from 0.12 to 0.22 mg/L. Moreover, corrosivity ratio indicated that water from the majority of sources (71%) is safe to supply using pipes without any corrosive effects, while 29% of sources are corrosive in nature and need non-corrosive pipes for transporting and lifting of groundwater. The results revealed, groundwater samples were within permissible limits as prescribed by International and National standards, for drinking purposes. The State government and NGO’s can show their interest in utilizing such water resources to overcome the shortage of drinking water in a sustainable way for the daily consumption of the people living in the vicinity of Jhelum River.  相似文献   

20.
Groundwater hydrochemistry could reveal the interaction mechanism between groundwater and the environment, which provides a scientific basis for environmental resources management. In this study, Shukaliefu’s classification method and Piper diagram were adopted to determine the hydrochemical types of groundwater in the Tarim Basin of Xinjiang, China. The method of “one-vote veto” was applied to evaluate the quality of groundwater. Phreeqc software was used to calculate the saturation indices of calcite and fluorite in groundwater. By comparing groundwater quality data of 2003 and 2011, we characterized the variations in hydrochemical types and water quality types, salinization of groundwater and fluoride geochemistry of the plain area of the Tarim Basin. Results show that the primary anion in phreatic water in the plain area of the Tarim Basin changed from HCO3 ? to SO4 2? or Cl?. On the contrary, the primary anion in confined water changed from SO4 2? or Cl? to HCO3 ?. In 2003, 63.1 % of the sampling points in the study area exceeded the Class III water quality standard of China. In 2011, the proportion increased to 82.5 %. In addition, severe groundwater salinization was found at 19.7 % of the sampling points. Some of the deep groundwater samples were salinized as well. In the Aksu area at the north-west part of the Tarim Basin, F? concentration exceeding the standard limit (1 mg/L) was found to be 55.0 % of the groundwater samples tested. Based on these findings, it is concluded that the phreatic water in the study area was severely influenced by the industrial wastewater and domestic sewage related to human activities, while the confined water was less affected. The general quality of groundwater was in an aggravation trend, and the groundwater salinization was in a severe condition in this area. The Ca2+–Na+ ionic exchange, the unsaturated fluorite and oversaturated calcite in the aquifer of the Aksu area are proposed to cause F? enrichment in groundwater of this area.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号