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1.
Hydogrochemical investigation of groundwater resources of Paragraph district has been carried out to assess the solute acquisition processes and water quality for domestic and irrigation uses. Fifty-five groundwater samples were collected and analyzed for pH, electrical conductivity, total dissolved solids, hardness, major anions (F?, Cl?, NO3, HCO3 ?, SO4 2?) and cations (Ca2+, Mg2+, Na+, K+). Study results reveal that groundwater of the area is alkaline in nature and HCO3 ?, Cl?, Mg2+, Na+ and Ca2+ are the major contributing ions to the dissolved solids. The hydrogeochemical data suggest that weathering of rock forming minerals along with secondary contributions from agricultural and anthropogenic sources are mainly controlling the groundwater composition of Pratapgarh district. Alkaline earth metals (Ca2++Mg2+) exceed alkalis (Na++K+) and weak acid (HCO3 ?) dominate over strong acids (Cl?+SO4 2?) in majority of the groundwater samples. Ca-Mg-HCO3 and Ca-Mg-Cl-HCO3 are the dominant hydrogeochemical facies in the groundwater of the area. The computed saturation indices demonstrate oversaturated condition with respect to dolomite and calcite and undersaturated with gypsum and fluorite. A comparison of groundwater quality parameters in relation to specified limits for drinking water shows that concentrations of TDS, F?, NO3 ? and total hardness exceed the desirable limits in many water samples. Quality assessment for irrigation uses reveal that the groundwater is good for irrigation. However, values of salinity, sodium adsorption ratio (SAR), residual sodium carbonate (RSC), %Na and Kelley index are exceeding the prescribed limit at some sites, demanding adequate drainage and water management plan for the area.  相似文献   

2.
In this study, 92 groundwater samples were collected from the Attica region (Greece). Moreover, geographical information system database, geochemistry of groundwater samples and statistics were applied. These were used for studying the chemical parameters (NO3 −, Mg2+, Ca2+, Cl−, and Na+) and conductivity spatial distribution and for assessing their environmental impact. The ranges of chemical parameters of the water samples (in mg L−1) are: NO3 − 1–306, Mg2+ 2–293, Ca2+ 3–453, Cl− 5–1,988, and Na+ 4–475. The elevated concentrations of sodium, Mg2+, Cl− are attributed to natural contamination (seawater intrusion). On the other hand, NO3 − elevated concentrations are attributed to anthropogenic contamination (nitrate fertilizers). The results of the GIS analysis showed that elevated values of Na+, Mg2+, Cl− are related to shrubby and sparsely vegetated areas, while elevated values of NO3 − are connected with urban and agricultural areas.  相似文献   

3.
A survey on quality of groundwater was carried out for assessing the geochemical characteristics and controlling factors of chemical composition of groundwater in a part of Guntur district, Andhra Pradesh, India, where the area is underlain by Peninsular Gneissic Complex. The results of the groundwater chemistry show a variation in pH, EC, TDS, Ca2+, Mg2+, Na+, K+, HCO3 ?, Cl?, SO4 2?, NO3 ? and F?. The chemical composition of groundwater is mainly characterized by Na+?HCO3 ? facies. Hydrogeochemical type transits from Na+–Cl?–HCO3 ? to Na+–HCO3 ?–Cl? along the flow path. Graphical and binary diagrams, correlation coefficients and saturation indices clearly explain that the chemical composition of groundwater is mainly controlled by geogenic processes (rock weathering, mineral dissolution, ion exchange and evaporation) and anthropogenic sources (irrigation return flow, wastewater, agrochemicals and constructional activities). The principal component (PC) analysis transforms the chemical variables into four PCs, which account for 87% of the total variance of the groundwater chemistry. The PC I has high positive loadings of pH, HCO3 ?, NO3 ?, K+, Mg2+ and F?, attributing to mineral weathering and dissolution, and agrochemicals (nitrogen, phosphate and potash fertilizers). The PC II loadings are highly positive for Na+, TDS, Cl? and F?, representing the rock weathering, mineral dissolution, ion exchange, evaporation, irrigation return flow and phosphate fertilizers. The PC III shows high loading of Ca2+, which is caused by mineral weathering and dissolution, and constructional activities. The PC IV has high positive loading of Mg2+ and SO4 2?, measuring the mineral weathering and dissolution, and soil amendments. The spatial distribution of PC scores explains that the geogenic processes are the primary contributors and man-made activities are the secondary factors responsible for modifications of groundwater chemistry. Further, geochemical modeling of groundwater also clearly confirms the water–rock interactions with respect to the phases of calcite, dolomite, fluorite, halite, gypsum, K-feldspar, albite and CO2, which are the prime factors controlling the chemistry of groundwater, while the rate of reaction and intensity are influenced by climate and anthropogenic activities. The study helps as baseline information to assess the sources of factors controlling the chemical composition of groundwater and also in enhancing the groundwater quality management.  相似文献   

4.
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   

5.
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   

6.
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   

7.
One hundred forty-eight groundwater samples were collected from the lower part of Wadi Siham catchment area for hydrogeochemical investigations to understand the hydrogeochemical processes affecting groundwater chemistry and their relation with groundwater quality. Groundwater in the study area is abstracted from different aquifers. The study area is characterized by arid climate and extremely high relative humidity. The results indicate that groundwater in the study area is fresh to brackish in nature. The abundance of the major ions is as follows: Na+1?>?Ca+2?>?Mg+2?≥?K+1 and Cl?1?>?HCO 3 ?1 ?>?SO 4 ?2 ?>?NO 3 ?1 . Various graphical and ionic ration plots, statistical analyses, and saturation indices calculations have been carried out using chemical data to deduce a hydrochemical evaluation of the study area. The prevailing hydrogeochemical processes operating in the study area are dissolution, mixing, evaporation, ion exchange, and weathering of silicate minerals in the eastern part (recharge areas). The reverse ion exchange and seawater intrusion control the groundwater chemistry along the Red Sea coast areas and few parts of the study area. Deterioration in groundwater quality from anthropogenic activities has resulted from saltwater intrusion along the coastal areas due to groundwater overpumping and extensive use of fertilizers and infiltration of sewage water. Salinity and nitrate contamination are the two major problems in the area, which is alarming considering the use of this water for drinking.  相似文献   

8.
Agricultural activities act as dominant polluter of groundwater due to increased fertilizers and pesticides usage. Bist-Doab region, Punjab, India, is one such region facing deterioration of groundwater quality due to usage of fertilizers. This study aims in delineating and evaluating the groundwater quality in the region. Water samples are collected from canals, reservoir, and shallow and deep groundwater. Water types in canal and reservoir in Kandi region are Mg2+HCO3 ? and Mg2+Ca2+Na+HCO3 ?, respectively. While water types of shallow and deep groundwaters are found to be of two types: Na+Mg2+Ca2+HCO3 ? and Ca2+Mg2+Na+HCO3 ?. Presence of Mg2+ in groundwater at locations adjoining canals indicates recharge due to canal. The major ion (Na+, Mg2+, Ca2+, HCO3 ?) chemistry of the region is due to weathering of rocks that are rich in sodic minerals and kankar. Deep groundwater quality in the region meets BIS and WHO standards for drinking purpose, unlike shallow groundwater which is of poor quality at many locations. Both shallow and deep groundwater with high sodium concentration (>1.5 meq/l) affect cropping yield and permeability of soil matrix. High concentration of SO4 2? and NO3 2? (>1 meq/l) in shallow groundwater at few locations indicates influence of anthropogenic (fertilizer) activity. Factor analysis indicates that the major cations, bicarbonate and chloride are derived from weathering/dissolution of source rocks. Higher concentration of nitrate and presence of sulphate in shallow groundwater at few locations is due to usage of fertilizers and pesticides.  相似文献   

9.
The study of groundwater hydrogeochemistry of a hard rock aquifer system in Thoothukudi district has resulted in a large geochemical data set. A total of 100 water samples representing various lithologies like Hornblende Biotite Gneiss, Alluvium Marine, alluvium Fluvial, Quartzite, Charnockite, Granite and Sandstone were collected for two different seasons and analyzed for major ions like Ca2+, Mg2+, Na+, K+, HCO3 ?, Cl?, SO4 2?, NO3 ?, PO4 ?, F? and H4SiO4. Statistical analysis of the data has been attempted to unravel the hidden relationship between ions. Correlation analyses and factor analyses were applied to classify the groundwater samples and to identify the geochemical processes controlling groundwater geochemistry. Factor analysis indicates that sea water intrusion followed by leaching of secondary salts, weathering and anthropogenic impacts are the dominant factors controlling hydrogeochemistry of groundwater in the study area. Factor score overlay indicate major active hydrogeochemical regimes are spread throughout the Eastern, Northwestern and Southeastern parts of the study area. The dominant ions controlling the groundwater chemistry irrespective of season are Cl?, Na+, Mg2+, Ca2+, SO4 2?, K+ and NO3 ?. An attempt has also been made to note the seasonal variation of the factor representations in the study area. This study also illustrates the usefulness of statistical analysis to improve the understanding of groundwater systems and estimates of the extent of salinity/salt water intrusion.  相似文献   

10.
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   

11.
 This paper describes the origins and distribution of saline groundwaters in the coastal area of Rhodope, Greece. The aquifer system includes two aquifers within coarse-grained alluvial sediments in the coastal part of the study area. Two major water-quality groups occur in the study area, namely Ca2+-rich saline groundwater and Ca2+-poor, almost fresh groundwater. The main process controlling the groundwater chemistry is the exchange of calcium and sodium between the aquifer matrix and intruding seawater. The natural salt water in the study area is probably residual water that infiltrated the aquifer system during repeated marine transgressions in late Pleistocene time. Seawater intrusion into the coastal aquifer system occurs as a result of overpumping in two seawater wedges separated vertically by a low-permeability layer. The rate of intrusion averages 0.8 m/d and is less than expected due to a decline of the aquifer's permeability at the interface with the seawater. The application of several hydrochemical techniques (Piper and Durov diagrams; Na+/Cl–, Ca2+/Cl–, Mg2+/Cl–, and Br–/Cl– molar ratios; Ca2+/Mg2+ weight ratio; and chloride concentrations), combined with field observations, may lead to a better explanation of the origin of the saline groundwater. Received, May 1997 / Revised, May 1998, December 1998 / Accepted, February 1999  相似文献   

12.
Groundwater samples collected from the East Bokaro coalfield of Jharkhand state, India during the dry and rainy seasons of the year 2012. Samples were analyzed for the assessment of groundwater quality in the study area. The results of the chemical analysis indicate that the pH values were found alkaline in nature during both the season. The major cations in groundwater was in the order of Na+>Ca2+>Mg2+>K+ during the dry season while Ca2+>Na+>Mg2+>K+ during the rainy season. The abundance of the major anions was of HCO3->SO42->Cl->NO3->F- did not change on the seasonal basis. The average NO3-concentration was exceeded the desirable limit for drinking water as per Indian standard in the rainy season. Silicate weathering was inferred to be a dominant process, controlling the groundwater chemistry in both seasons, with lesser contributions by carbonate weathering and ion exchange. Leaching of salts from the unsaturated zone also has a major impact on groundwater quality during the rainy season. The water quality data indicate that groundwater is generally suitable for irrigation. However, higher salinity and residual sodium carbonate values at some sites may limit groundwater use and therefore an adequate drainage and water management plan for the study area is required.  相似文献   

13.
The Narava basin in Visakhapatnam district situated on the east coast is a productive agricultural area, and is also one of the fastest growing urban areas in India. The agricultural and urban-industrialization activities have a lot of impact on this coastal aquifer water quality. The hydrochemistry of the groundwater was analyzed in the basin area with reference to drinking and agricultural purposes. The area is underlain by Precambrian rocks like khondalites, charnockites and migmatites. The water samples were collected from shallow wells for the year 2008. Physical and chemical parameters of groundwater such as pH, total alkalinity (TA), electrical conductivity (EC), total dissolved solids (TDS), total hardness (TH), Ca2+, Mg2+, Na+, K+, HCO3 ?, Cl?, SO4 2?, NO3 ?, F? were determined. The analytical results revealed that the most of the groundwater found to be in polluted category. Geographical information system (GIS) was utilized to generate different spatial distribution maps of various chemical constituents in the study area. The analytical data were used to compute certain parameters such as salinity hazard, percent sodium (Na%), sodium adsorption ratio (SAR), residual sodium carbonate (RSC), permeability index (PI), Kelley??s ratio (KR) and corrosivity ratio (CR) to determine the quality of water for agricultural purposes. The abundance of the major ions in the basin area was found to be in the following sequence: Na+?>?Ca2+?>?Mg2+?>?K+:Cl??>?HCO3 ??>?SO4 2??>?NO3 ??>?F?. According to Gibbs?? diagram most of the samples fall under rock dominance. As per Wilcox and USSL classification most of the groundwater samples are suitable for irrigation except few samples which are unsuitable due to the presence of high salinity and high sodium hazard. From the obtained data, it can be concluded that the water quality profile was good and useful for normal irrigation agriculture.  相似文献   

14.
The hydrogeochemical study of groundwater in Dumka and Jamtara districts has been carried out to assess the major ion chemistry, hydrogeochemical processes and groundwater quality for domestic and irrigation uses. Thirty groundwater samples were collected and analyzed for pH, electrical conductivity, total dissolved solids (TDS), total hardness, anions (F?, Cl?, NO3 ?, HCO3 ?, SO4 2?) and cations (Ca2+, Mg2+, Na+, K+). The analytical results show the faintly alkaline nature of water and dominance of Mg2+ and Ca2+ in cationic and HCO3 ? and Cl? in anionic abundance. The concentrations of alkaline earth metals (Ca2+?+?Mg2+) exceed the alkali metals (Na+?+?K+) and HCO3 ? dominates over SO4 2??+?Cl? concentrations in the majority of the groundwater samples. Ca?CMg?CHCO3 is the dominant hydrogeochemical facies in 60?% of the groundwater samples, while 33?% samples occur as a mixed chemical character of Ca?CMg?CCl hydrogeochemical facies. The water chemistry is largely controlled by rock weathering and ion exchange processes with secondary contribution from anthropogenic sources. The inter-elemental correlations and factor and cluster analysis of hydro-geochemical database suggest combined influence of carbonate and silicate weathering on solute acquisition processes. For quality assessment, analyzed parameter values were compared with Indian and WHO water quality standards. In majority of the samples, the analyzed parameters are well within the desirable limits and water is potable for drinking purposes. Total hardness and concentrations of TDS, Cl?, NO3 ? , Ca2+ and Mg2+ exceed the desirable limits at a few sites, however, except NO3 ? all these values were below the highest permissible limits. The calculated parameters such as sodium adsorption ratio, percent sodium (%Na) and residual sodium carbonate revealed excellent to good quality of groundwater for agricultural purposes, except at few sites where salinity and magnesium hazard (MH) values exceeds the prescribed limits and demands special management.  相似文献   

15.
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   

16.
Based on the analysis of element correlation, the Gibbs diagram, hydro-geochemical ion ratios, isoline maps of groundwater and soil, and change patterns of strontium content after normalization, the study examines water-rock interaction of shallow groundwater in Dingtao area. The results suggest that strontium in the study area mainly comes from water-rock interactions, and the strata interacting with groundwater are the top of Quaternary and Neogene. The element correlation analysis shows that the formation of strontium-rich groundwater is sufficiently affected by sulfate and carbonate. The Gibbs diagram suggests that the chemical composition of groundwater is mainly influenced by water-rock interactions, accompanied by evaporation crystallization. c(Ca2++Mg2+)/c(HCO3-+SO42-) reflects that the main reactions in the groundwater system is weathering dissolution of carbonate and sulfate, and ion exchange takes place. c(Na+)/c(Cl-) indicates that Na+ in groundwater may have water-rock interactions with rocks it flows through. c(Cl-)/c(Ca2+) indicates that the hydrodynamic condition in the pumping well is poor and the water circulation is slow. The study examines the macro isoline map change patterns, correlation curves of change of strontium content in groundwater and shallow soil, and correlation curves of change of strontium content in groundwater, shallow soil, and deep soil. The results suggest that the strontium content in the study area has the same change pattern in groundwater and in soil, which further indicates that strontium in the study area comes from water-rock interactions.  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.
Soil salinization is an environmental problem having significant impacts on the soil–water–plant system. This problem is more frequent in coastal areas due to seawater intrusion into the land. Assessing the soil salinization is a critical issue for the agricultural areas situated in the Mediterranean basin. This paper examines the deterioration of soil quality in the cultivated land of a Mediterranean site (Agoulinitsa district—West Greece). Soil samples were collected in both pre-irrigation and post-irrigation seasons. Electrical conductivity (EC), pH and the ions Br?, Ca2+, Cl?, F?, K+, Li+, Mg2+, Na+, NH4 +, NO2 ?, NO3 ?, PO4 3? and SO4 2? were determined by the 1:2 (soil/water ratio on weight basis) method. The salts which were present in both seasons in the soils of the area studied are KCl, MgCl2, NaCl, CaSO4 and K2SO4. The wide spatiotemporal variation of EC in the cultivated land in both seasons demonstrates that soil salinity is controlled mainly by seawater intrusion and anthropogenic factors such as the application of salt-rich water which is directly pumped from the drainage ditches. Seawater intrusion provides the affected soil with elevated contents of Ca2+, Cl?, K+, Mg2+, Na+ and SO4 2?. Classification of the soils by using criteria given by the literature is discussed. Practices to prevent, or at least ameliorate, salinization in the cultivated land of Agoulinitsa district are proposed.  相似文献   

19.
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   

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