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1.
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   

2.
The present study aims to discuss the hydrogeochemical processes in the Aosta Valley region and assess the quality of its groundwater for suitability of drinking and irrigation purposes. One hundred twenty-two samples were collected from the Aosta Valley region in the years 2007 and 2008 (61 per year), and analysed for pH, electrical conductivity, total dissolved solids (TDS), total hardness, major cations and anions. The pH of the samples in both years indicated a near-neutral to alkaline nature of the groundwater. The cation and anion chemistry showed the general ionic abundance as: Ca2+ > Mg2+ > Na+ > K+ and HCO3 ?>SO4 2?>Cl?>NO3 ?>F? in both years. Ca2+-Mg2+-HCO3 ? and Ca2+-Mg2+-Cl?-SO4 2? were the dominant hydrogeochemical facies. The computed saturation indices demonstrated that the groundwater was supersaturated with respect to dolomite and calcite in both years. The groundwater chemistry of the study area was mainly controlled by the dissolution of carbonate, sulphate and silicate minerals, as well as ion exchange processes. A comparison of the groundwater quality in relation to drinking water standards showed that most of the water samples were suitable for drinking and domestic uses. The computed water quality index (WQI) values of the study area groundwater ranged from 24 to 84 in the year 2007 and from 22 to 82 in the year 2008, and all the location fell under the Excellent to Good category. Quality assessment for irrigation uses revealed that the groundwater was good to permissible quality for irrigation; however, locally higher salinity, residual sodium carbonate (RSC) and magnesium hazard (MH) restricted its suitability for irrigation at a few sites. These results will be useful in implementing future measures in groundwater resource management at regional and national level.  相似文献   

3.
Groundwater from karst subterranean streams is among the world’s most important sources of drinking water supplies, and the hydrochemical characteristics of karst water are affected by both natural environment and people. Therefore, the study of karst groundwater hydrochemistry and its solutes’ sources is very important to ensure the normal function of life support systems. This paper focused on the major ion chemistry and sulfate isotope of karst groundwater in Chongqing for tracing the sulfate sources and related hydrochemical processes. Hydrochemical types of karst groundwater in Chongqing were mainly of the Ca-HCO3 type or Ca(Mg)-HCO3 type. However, some hydrochemical types were the K + Na + Ca-SO4 type (G25 site) or Ca-HCO3 + SO4 type (G26 and G14 sites), indicating that the hydrochemistry of these sites may be strongly influenced by anthropogenic activities or unique geological characteristics. The δ34S-SO4 2? of collected karst groundwater sample fell into a range of ?6.8 to 21.5 ‰, with a mean value of 5.6 ‰. In dolomite aquifer, the δ34S-SO4 2? value ranges from ?4.3 to 11.0 ‰, and in limestone aquifer, it ranged from ?6.8 to 21.5 ‰. The groundwater samples from different land use types showed distinctive δ34S-SO4 2? value. The δ34S-SO4 2? value of groundwater samples had range of ?6.8 to 16.7 ‰ (mean 4.0 ‰, n = 11) in cultivated land areas, 1.5–21.5 ‰ (mean 7.2 ‰, n = 20) in forested land areas, and ?4.3 to 0.8 ‰ (mean ?1.7 ‰, n = 2) in coalmine areas. The δ34S-SO4 2? values of groundwater samples collected from factory area and town area were 2.2 and 9.9 ‰, respectively. According to the δ34S information of potential sulfate sources, this paper discussed the possible sulfate sources of collected karst groundwater samples in Chongqing. The variations of both δ34S and 1/SO4 2? values of the groundwater samples indicated that the atmospheric acid deposition (AAD), dissolution of gypsum (GD), oxidation of sulfide mineral (OS) or anthropogenic inputs (SF: sewage or fertilizer) contributed to sulfate in karst groundwater. The influence of oxidation of sulfide mineral, atmospheric acid deposit and anthropogenic inputs to groundwater in Chongqing karst areas was much widespread. For protecting, sustaining, and utilizing the groundwater resources, the sewage possibly originating from urban, mine or industrial area must be controlled and treated, and the use of fertilizer should be limited.  相似文献   

4.
Calcite (CaCO3), dolomite [CaMg(CO3)2], silicate dissolution, ion-exchange and reverse ion-exchange reactions are the predominant processes influencing groundwater quality in the Savelugu?CNanton District. The main objective of this study is to characterize groundwater and delineate water?Crock interactions responsible for the chemical evolution of groundwater in the District. Eighty-one (81) boreholes were sampled for quality assessment. Results showed that, the pH of the boreholes are slightly acidic to basic ranging from 6.1?C8.3?pH units. Conductivity values are low to high ranging from 147?C23,200???S/cm with, 23.5?% of groundwater within the study area being either brackish (1,500?C5,000???S/cm) or saline (>5,000???S/cm) and therefore, unsuitable for potable purposes. TDS values in groundwater varied widely, ranging from 62?C11,900?mg/L. 61.7?% of groundwater within the study area are fresh (TDS?<?500?mg/L). The chemical constituents generally, have low concentrations and are within the WHO (Guidelines for drinking water quality. Revision of the 1993 Guidelines. Final Task Group Meeting. Geneva, 2004) Guideline values. The relative abundance of cations and anions in the groundwater are in the order: Ca2+?>?Na+?>?Mg2+?>?K+ and HCO3 ??>?Cl??>?SO4 2??>?NO3 ? respectively. Multivariate statistical analysis showed expected process-based relationship derived mainly from the geochemical and biochemical processes within the aquifer. Hydrochemical facies using piper plot of major ions showed one major hydrochemical water type. The Ca?CMg?CHCO3 water type. Due to the high cost of drilling of boreholes coupled with the high percentage (×1?%) of people without access to potable water in the Northern Region, it is recommended that the Government of Ghana and other stakeholders within the Water Sector take immediate measures to reduce (to recommended limits for potable uses) the levels of dissolved solids either by installing Reverse Osmosis equipments on such boreholes or employ other relatively known cheaper methods to reduce the dissolved solids to recommended limits. High yielding boreholes with hydrochemical parameters within WHO guideline limits in the Savelugu?CNanton District could also be mechanized to serve a wider area.  相似文献   

5.

Progressive developments in industrial and agricultural activities are causing a critical stress on groundwater quality in developing countries. The objective of this paper is to assess and evaluate the contamination level of groundwater caused by leachate in 11 villages of the Gautam Budh Nagar district in Uttar Pradesh, India. We systematically sampled 22 groundwater samples and 13 leachate samples to ascertain the source of pollution on groundwater quality. The standard analytical methods given by the American Public Health Association (APHA) (Standard methods for examination of water and wastewater, 23rd edn. APHA, AWWA, WPCF, Washington, 2017) were used for quantitative estimation of hydrochemical parameters of collected samples. The results of the analysis of groundwater samples indicate that pH values range from 7.31 to 8.97. The mean magnesium concentration in groundwater samples is 58.93 ± 21.44 mg/L. Out of the groundwater samples taken, approximately 41% and 73% of samples analysis results have been found beyond the acceptable limit with respect to the parameters of turbidity and total dissolved solids, respectively, according to the Bureau of Indian Standards (Indian standard specification for drinking water (IS:10500). BIS, Manak Bhawan, New Delhi, 2012) for drinking water. Around 95.4% of groundwater samples and 92.3% of leachate samples have high nitrate concentrations above the standard limit of BIS (45 mg/L), respectively. The Piper plot shows that 50% of the samples belong to the Ca2+–Mg2+–HCO3 type. Ternary and Durov’s diagrams indicate that the mean concentrations of ions are in the order of Na+ > Mg2+ > Ca2+ > K+ (for cations) and HCO3> NO3 > Cl > SO42− > CO32− > F (for anions) in groundwater of the study area. The spatial variation of the hydrochemical parameters shows that groundwater is heavily contaminated with respect to nitrate. Analytical results indicate that the groundwater of villages Achheja, Bisrakh road, Dujana, Badalpur and Sadopur is not suitable for drinking.

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6.
7.
Groundwater is a vital source for domestic and irrigation purposes in the loess area of Northwest China where climate is arid. However, the quality of groundwater in this area is deteriorating due to intensive industrial and agricultural activities, and this has a great adverse impact on human health. In order to better understand the pollution status of groundwater and the health risks to local residents, comprehensive water quality index was applied to assess the quality of drinking water in Yulin City, Northwest China, and sodium adsorption ratio, sodium percentage, residual sodium carbonate and permeability index were used to evaluate the quality of irrigation water. Moreover, the health risks caused by ingestion of groundwater were evaluated using the model proposed by the Ministry of Environmental Protection of the PR China. The results show that all groundwater samples for irrigation will not induce soil salinization, but more than half of them are not suitable for drinking, and Fe, Mn, TH, Mg2+ and NO3–N are the common contaminants which are mainly from natural processes, industrial and agricultural activities. The health risk assessment indicates that children face greater non-carcinogenic risk than adults. The order of contribution of contaminants to non-carcinogenic risk is NO3 ? > As > F? > Fe > Mn > Ba2+ > Cr6+ > Zn > NO2 ?. The average carcinogenic risk of carcinogens (Cr6+ and As) is 1.17 × 10?4 and 1.37 × 10?4 for adults and children, respectively, which surpasses the permissible level (1 × 10?6) stipulated by the Ministry of Environmental Protection of the PR China. Hence, effective measures are highly demanded to manage groundwater pollution and reduce the risks to human health.  相似文献   

8.
The concentrations of uranium, iron and the major constituents were determined in groundwater samples from aquifer containing uranyl phosphate minerals (meta-autunite, meta-torbernite and torbernite) in the Köprüba?? area. Groundwater samples from wells located at shallow depths (0.5–6 m) show usually near neutral pH values (6.2–7.1) and oxidizing conditions (Eh = 119–275 mV). Electrical conductivity (EC) values of samples are between 87 and 329 μS/cm?1. They are mostly characterized by mixed cationic Ca dominating bicarbonate types. The main hydrogeochemical process is weathering of the silicates in the shallow groundwater system. All groundwater in the study area are considered undersaturated with respect to torbernite and autunite. PHREEQC predicted UO2(HPO4) 2 2? as the unique species. The excellent positive correlation coefficient (r = 0.99) between U and PO4 indicates the dissolved uranium in groundwater would be associated with the dissolution of uranyl phosphate minerals. The groundwater show U content in the range 1.71–70.45 μg/l but they are mostly lower than US EPA (2003) maximum contaminant level of 30 μg/l. This low U concentrations in oxic groundwater samples is attributed to the low solubility of U(VI) phosphate minerals under near neutral pH and low bicarbonate conditions. Iron closely associated with studied sediments, were also detected in groundwater. The maximum concentration of Fe in groundwater samples was 2837 μg/l, while the drinking water guidelines of Turkish (TSE 1997) and US EPA (2003) were suggested 200 and 300 μg/l, respectively. Furthermore, iron and uranium showed a significant correlation to each other with a correlation coefficient (r) of 0.94. This high correlation is probably related to the iron-rich sediments which contain also significant amounts of uranium mineralization. In addition to pH and bicarbonate controlling dissolution of uranyl phosphates, association of uranyl phosphates with iron (hydr) oxides seems to play important role in the amount of dissolved U in shallow groundwater.  相似文献   

9.
Groundwater in Farashband plain, Southern Iran, is the main source of water for domestic and agricultural uses. This study was carried out to assess the overall water quality and identify major variables affecting the groundwater quality in Farashband plain. The hydrochemical study was undertaken by randomly collecting 84 groundwater samples from observation wells located in 13 different stations covering the entire plain in order to assess the quality of the groundwater through analysis of major ions. The water samples were analyzed for various physicochemical attributes. Groundwater is slightly alkaline and largely varies in chemical composition; e.g., electrical conductivity (EC) ranges from 2314 to 12,678 μS/cm. All the samples have total dissolved solid values above the desirable limit and belong to a very hard type. The abundance of the major ions is as follows: Na+ > Ca2+ > Ma2+ > K+ and Cl? > SO4 2– > HCO3 ?. Interpretation of analytical data shows three major hydrochemical facies (Ca–Cl, Na–Cl, and mixed Ca–Mg–Cl) in the study area. Salinity, total dissolved solids, total hardness, and sodium percentage (Na%) indicate that most of the groundwater samples are not suitable for irrigation as well as for domestic purposes and far from drinking water standard. A comparison of groundwater quality in relation to drinking water standards showed that most of the water samples are not suitable for drinking purposes. Based on the US salinity diagram, most of samples belong to high salinity and low to very high sodium type.  相似文献   

10.
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   

11.
The chemical analysis of 19 water wells in Ferdows area, Northeastern Iran, has been evaluated to determine the hydrogeochemical processes and ion concentration background in the region. In the study area, the order of cation and anion abundance is Na+ > Ca2+ > Mg2+ > K+ and Cl? > SO 4 ?2  > HCO3 ? > NO3 ?, respectively, and the dominating hydrochemical types are Na–Cl. Most metal concentrations in water depend on the mineral solubility, and pH, Eh, and salinity of the solution. Their ΣREE concentrations showed excellent correlations with parameters such as TDS and pH. North American Shale Composite (NASC)-normalized REE patterns are enriched in the HREEs relative to the LREEs for all groundwaters. They all have positive Eu anomalies (Eu/Eu* = 0.752–3.934) and slightly negative Ce anomalies (Ce/Ce* = 0.019–1.057). Reduction–oxidation, complexation, desorption, and re-adsorption alter groundwater REE concentrations and fractionation patterns. The positive Eu anomalies in groundwaters are probably due to preferential mobilization of Eu2+ relative to the trivalent REEs in the reducing condition.  相似文献   

12.
A total of 129 groundwater samples were collected in the Jangseong region of South Korea to characterize and evaluate groundwater quality and its suitability for irrigation and domestic uses. Samples were chemically analyzed for major ions, pH, electrical conductivity, and total dissolved solids following standard methods. The AquaChem 2014.2 model linked with PHREEQC was used for the statistical analysis and characterization of the hydrochemistry of the groundwater. The analysis showed that in all samples Ca–HCO3 was the leading water type and that the abundance of major cations was in the order Ca > Na > Mg > K, and of anions in the order HCO3 > Cl > SO4 > F. According to the correlation analysis, Ca showed strong interdependence with HCO3, suggesting that these parameters may have originated from common sources. Saturation index calculations indicated that all samples were undersaturated with respect to aragonite, calcite, dolomite, fluorite, gypsum, halite, and siderite, and oversaturated with respect to goethite and hematite. The irrigation suitability analysis revealed that groundwater in the Jangseong area can be used for irrigation without any restrictions based on EC, sodium adsorption ratio, percent sodium, residual sodium carbonate, Kelley ratio, permeability index, and the US Salinity Laboratory diagram analysis. The drinking water suitability analysis made for major parameters by comparison with the WHO guidelines indicates that the groundwater in the area is suitable for drinking except in some samples with high nitrate–N concentrations. The elevated nitrate concentrations in the groundwater are likely an indicator of agricultural pollution.  相似文献   

13.
Groundwater is an important water source for agricultural irrigation in Penyang County. Some traditional methods such as irrigation coefficient, sodium adsorption ratio, total alkalinity, total salinity and total dissolved solids were employed to assess groundwater quality in this area. In addition, an improved technique for order preference by similarity to ideal solution model was applied for comprehensive assessment. The origin of major ions and groundwater hydrogeochemical evolution was also discussed. Groundwater in Penyang County contains relative concentrations of dominant constituents in the following order: Na+ > Ca2+ > Mg2+ > K+ for cations and HCO3 ? > SO4 2? > Cl? > CO3 2? for anions. Groundwater quality is largely excellent and/or good, suggesting general suitability for agricultural use. Calcite and dolomite are found saturated in groundwater and thus tend to precipitate out, while halite, fluorite and gypsum are unsaturated and will dissolve into groundwater during flow. Groundwater in the study area is weathering-dominated, and mineral weathering (carbonate and silicate minerals) and ion exchange are the most important factors controlling groundwater chemistry.  相似文献   

14.
15.
This study is the first investigation of biodegradation of carbon disulphide (CS2) in soil that provides estimates of degradation rates and identifies intermediate degradation products and carbon isotope signatures of degradation. Microcosm studies were undertaken under anaerobic conditions using soil and groundwater recovered from CS2-contaminated sites. Proposed degradation mechanisms were validated using equilibrium speciation modelling of concentrations and carbon isotope ratios. A first-order degradation rate constant of 1.25 × 10?2 h?1 was obtained for biological degradation with soil. Carbonyl sulphide (COS) and hydrogen sulphide (H2S) were found to be intermediates of degradation, but did not accumulate in vials. A 13C/12C enrichment factor of ?7.5 ± 0.8 ‰ was obtained for degradation within microcosms with both soil and groundwater whereas a 13C/12C enrichment factor of ?23.0 ± 2.1 ‰ was obtained for degradation with site groundwater alone. It can be concluded that biological degradation of both CS2-contaminated soil and groundwater is likely to occur in the field suggesting that natural attenuation may be an appropriate remedial tool at some sites. The presence of biodegradation by-products including COS and H2S indicates that biodegradation of CS2 is occurring and stable carbon isotopes are a promising tool to quantify CS2 degradation.  相似文献   

16.
Major ions and important trace elements in addition to δ18O and δ2H were analysed for 43 groundwater samples sampled from the Al-Batin alluvial fan aquifer, South Iraq. The most dominant ions (with respect to molarity) were: Na+ > Cl? > SO4 2? > Ca2+ > Mg2+ > NO3 ? > HCO3 ?, with total dissolved solids (TDS) averaging 7855 mg/L. High concentrations were found for the trace elements U, Mo, V, B, Sr, and Cr. This study suggests a hydraulic connection exists near the fan apex between the uppermost part of the Al-Batin aquifer and the underlying Dammam aquifer by means of the Abu-Jir fault system. Except for the effects of extensive irrigation, fertilizer use, and poorly maintained sewers, the groundwater chemistry is mainly controlled by geological processes such as dissolution of evaporites and the enrichment of dissolved ions as a result of the high evaporation and low recharge rate. Furthermore, it is shown that the Kuwaiti fuel–oil burning during Gulf War in 1991 contributed to the enrichment of V and Mo in the studied aquifer. The spatial distribution of most ions appears to generally increase from the south-west towards the north-east, in the direction of groundwater flow. The stable isotopes show heavier values in groundwater with a gradually increasing trend in the direction of groundwater flow due to the decreasing depth to groundwater and thus increasing of evaporation from both groundwater or irrigation return water. Additionally, the stable isotope signature suggests that rainfall from sources in the Arabian Gulf and the Arabian Sea is the major source of recharge for the Al-Batin aquifer. Except for two samples of groundwater, all samples were not suitable for potable use according to the WHO standards. Most of the groundwater is suitable for some agricultural purpose and for livestock water supply. Apart from the high salinity, boron represents the most critical element in the groundwater with respect to agricultural purposes.  相似文献   

17.
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   

18.
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   

19.
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   

20.
The hydrogeochemistry and isotope geochemistry of groundwater from 85 wells in fractured dolomite aquifers of Central Slovenia were investigated. This groundwater represents waters strongly influenced by chemical weathering of dolomite with an average of δ13CCARB value of +2.2 ‰. The major groundwater geochemical composition is HCO3 ? > Ca2+ > Mg2+. Several differences in hydrogeochemical properties among the classes of dolomites were observed when they were divided based on their age and sedimentological properties, with a clear distinction of pure dolomites exhibiting high Mg2+/Ca2+ ratios and low Na+, K+ and Si values. Trace element and nutrient concentrations (SO4 2?, NO3 ?) were low, implying that karstic and fractured dolomite aquifers are of good quality to be used as tap water. Groundwater was generally slightly oversaturated with respect to calcite and dolomite, and dissolved CO2 was up to 46 times supersaturated relative to the atmosphere. The isotopic composition of oxygen (δ18OH2O), hydrogen (δDH2O) and tritium ranged from ?10.3 to ?8.4 ‰, from ?68.5 to ?52.7 ‰ and from 3.5 TU to 10.5 TU, respectively. δ18O and δD values fell between the GMWL (Global Meteoric Water Line) and the MMWL (Mediterranean Meteoric Water Line) and indicate recharge from precipitation with little evaporation. The tritium activity in groundwater suggests that groundwater is generally younger than 50 years. δ13CDIC values ranged from ?14.6 to ?9.3 ‰ and indicated groundwater with a contribution of degraded organic matter/dissolved inorganic carbon in the aquifer. The mass balances for groundwater interacting with carbonate rocks suggested that carbonate dissolution contributes from 43.7 to 65.4 % and degradation of organic matter from 34.6 to 56.3 %.  相似文献   

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