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1.
Geochemical processes that take place in the aquifer have played a major role in spatial and temporal variations of groundwater quality. This study was carried out with an objective of identifying the hydrogeochemical processes that controls the groundwater quality in a weathered hard rock aquifer in a part of Nalgonda district, Andhra Pradesh, India. Groundwater samples were collected from 45 wells once every 2 months from March 2008 to September 2009. Chemical parameters of groundwater such as groundwater level, EC and pH were measured insitu. The major ion concentrations such as Ca2+, Mg2+, Na+, K+, Cl−, and SO4 2− were analyzed using ion chromatograph. CO3 − and HCO3 − concentration was determined by acid–base titration. The abundance of major cation concentration in groundwater is as Na+ > Ca2+ > Mg2+ > K+ while that of anions is HCO3 − > SO4 2− > Cl− > CO3 −. Ca–HCO3, Na–Cl, Ca–Na–HCO3 and Ca–Mg–Cl are the dominant groundwater types in this area. Relation between temporal variation in groundwater level and saturation index of minerals reveals the evaporation process. The ion-exchange process controls the concentration of ions such as calcium, magnesium and sodium. The ionic ratio of Ca/Mg explains the contribution of calcite and dolomite to groundwater. In general, the geochemical processes and temporal variation of groundwater in this area are influenced by evaporation processes, ion exchange and dissolution of minerals.  相似文献   

2.
Pollution of groundwater by seawater intrusion poses a threat to sustainable agriculture in the coastal areas of Korea. Therefore, seawater intrusion monitoring stations were installed in eastern, western, and southern coastal areas and have been operated since 1998. In this study, groundwater chemistry data obtained from the seawater intrusion monitoring stations during the period from 2007 to 2009 were analyzed and evaluated. Groundwater was classified into fresh (<1,500 μS/cm), brackish (1,500–3,000 μS/cm), and saline (>3,000 μS/cm) according to EC levels. Among groundwater samples (n = 233), 56, 7, and 37% were classified as the fresh, brackish, and saline, respectively. The major dissolved components of the brackish and saline groundwaters were enriched compared with those of the fresh groundwater. The enrichment of Na+ and Cl− was especially noticeable due to seawater intrusion. Thus, the brackish and saline groundwaters were classified as Ca–Cl and Na–Cl types, while the fresh groundwater was classified as Na–HCO3 and Ca–HCO3 types. The groundwater included in the Na–Cl types indicated the effects of seawater mixing. Ca2+, Mg2+, Na+, K+, SO4 2−, and Br− showed good correlations with Cl− of over r = 0.624. Of these components, the strong correlations of Mg2+, SO4 2−, and Br− with Cl− (r ≥ 0.823) indicated a distinct mixing between fresh groundwater and seawater. The Ca/Cl and HCO3/Cl ratios of the groundwaters gradually decreased and approached those of seawater. The Mg/Cl, Na/Cl, K/Cl, SO4/Cl, and Br/Cl ratios of the groundwaters gradually decreased, and were similar to or lower than those of seawater, indicating that Mg2+, Na+, K+, SO4 2−, and Br−, as well as Cl− in the saline groundwater can be enriched by seawater mixing, while Ca2+ and HCO3 − are mainly released by weathering processes. The influence of seawater intrusion was evaluated using threshold values of Cl− and Br−, which were estimated as 80.5 and 0.54 mg/L, respectively. According to these criteria, 41–50% of the groundwaters were affected by seawater mixing.  相似文献   

3.
The Heihe River Basin is a typical arid inland river basin for examining stress on groundwater resources in northwest China. The basin is composed of large volumes of unconsolidated Quaternary sediments of widely differing grain size, and during the past half century, rapid socio-economic development has created an increased demand for groundwater resources. Understanding the hydrogeochemical processes of groundwater and water quality is important for sustainable development and effective management of groundwater resources in the Heihe River basin. To this end, a total of 30 representative groundwater samples were collected from different wells to monitor the water chemistry of various ions and its quality for irrigation. Chemical analysis shows that water presents a large spatial variability of chemical facies (SO4 2−–HCO3−, SO4 2−–Cl−, and Cl−–SO4 2−) as groundwater flow from recharge area to discharge area. The ionic ratio indicates positive correlation between the flowing pairs of parameters: Cl− and Na+(r = 0.95), SO4 2− and Na+ (r = 0.84), HCO3 − and Mg2+(r = 0.86), and SO4 2− and Ca2+ (r = 0.91). Dissolution of minerals, such as halite, gypsum, dolomite, silicate, and Mirabilite (Na2SO4·10H2O) in the sediments results in the Cl−, SO4 2−, HCO3 −, Na+, Ca2+ and Mg2+ content in the groundwater. Other reactions, such as evaporation, ion exchange, and deposition also influence the water composition. The suitability of the groundwater for irrigation was assessed based on the US Salinity Laboratory salinity classification and the Wilcox diagram. The results show that most of the groundwater samples are suitable for irrigation uses barring a few locations in the dessert region in the northern sub-basin.  相似文献   

4.
About 24 samples from hand-dug wells and boreholes were used to characterize concentrations of the main inorganic ions in a laterite environment under semi-arid climatic conditions in Tikaré, northern Burkina Faso. It was found that the most represented groundwater anion in groundwater was HCO3 − with average levels of 49.1 mg/L in the dry season and 33.5 mg/L in the rainy season. The most represented cation was Ca2+ with mean concentrations of 13.7 and 9.5 mg/L, respectively. The main processes, which influence the concentrations of these ions, are evaporation (dry season), local enrichment of recharge water in some elements, ion exchange and fixation by clay minerals (in case of K+). The best correlations were found between Ca2+ and Mg2+ (r = 0.95), Cl− and Na+ (r = 0.95), HCO3 − and Mg2+ (r = 0.89), HCO3 − and Ca2+ (r = 0.89), and between HCO3 − and Na+ (r = 0.80). In general, the quality of the groundwater from the different wells sampled for this study was good enough to serve as drinking water. However, there were situations where the quality of water was polluted because of anthropogenic contaminants (mainly NO3 −, K+, Cl−) from septic tanks and manure pits located in the vicinity of some sampled wells. In addition, application of fertilizers also represents a potential anthropogenic contamination source with regard to SO4 2−, Ca2+, K+, Na+, and Mg2+. Considering the high concentrations of SO4 2−, Mg2+, Na+ and Ca2+ found in one borehole, the deeper, fractured aquifers were also likely to be enriched in these elements. In contrast, the shallow aquifers are likely to be contaminated with Cl−, NO3 − and K+. Cl− and K+ seem to be locally present in recharge water as shown by their relative higher mean concentrations in the rainy season samples.  相似文献   

5.
Hydrochemical investigations were carried out in Damagh area, Hamadan, western Iran, to assess chemical composition of groundwater. Forty representative groundwater samples were collected from different wells to monitor the water chemistry of various ions. Chemical analysis of the groundwater showed that the mean concentration of the cations is in the order Na+ > Ca2+ > Mg2+ > K+, while that for anions was HCO3− > Cl− > SO42 − > NO3−. All of the investigated groundwaters present two different chemical facies (Ca–HCO3 and Na–HCO3) which is in relation with their interaction with the geological formations of the basin, cation exchange between groundwater and clay minerals and anthropogenic activities. The principal component analysis (PCA) performed on groundwater identified three principal components controlling their variability in groundwater. Electrical conductivity, Mg2+, Na+, SO42−, and Cl− content were associated in the same component (PC1) (salinity), determined principally by anthropogenic activities. The pH, CO32 −, HCO3−, and Ca2+ (PC2) content were related to the geogenic factor. Finally, the NO3−, Cl− and K+ (PC3) were controlled by anthropogenic activity as a consequence of inorganic fertilizers.  相似文献   

6.
Muzaffarnagar is an economically rich district situated in the most fertile plains of two great rivers Ganga and Yamuna in the Indo-gangetic plains, with agricultural land irrigated by both surface water as well as groundwater. An investigation has been carried out to understand the hydrochemistry of the groundwater and its suitability for irrigation uses. Groundwater in the study area is neutral to moderately alkaline in nature. Chemistry of groundwater suggests that alkaline earths (Ca + Mg) significantly exceed the alkalis (Na + K) and weak acids exceed the strong acids (Cl + SO4), suggesting the dominance of carbonate weathering followed by silicate weathering. Majority of the groundwater samples (62%) posses Ca–Mg–HCO3 type of hydrochemical species, followed by Ca–Na–Mg–HCO3, Na–Ca–Mg–HCO3, Ca–Mg–Na–HCO3–Cl and Na–Ca–HCO3–SO4 types. A positive high correlation (r 2 = 0.928) between Na and Cl suggests that the salinity of groundwater is due to intermixing of two or more groundwater bodies with different hydrochemical compositions. Barring a few locations, most of the groundwater samples are suitable for irrigation uses. Chemical fertilizers, sugar factories and anthropogenic activities are contributing to the sulphate and chloride concentrations in the groundwater of the study area. Overexploitation of aquifers induced multi componential mixing of groundwater with agricultural return flow waters is responsible for generating groundwater of various compositions in its lateral extent.  相似文献   

7.
Sources of deep groundwater salinity in the southwestern zone of Bangladesh   总被引：2，自引：2，他引：0  
Twenty groundwater samples were collected from two different areas in Satkhira Sadar Upazila to identify the source of salinity in deep groundwater aquifer. Most of the analyzed groundwater is of Na–Cl–HCO3 type water. The trends of anion and cation are Cl− > HCO3 − > NO3 − > SO4 2− and Na+ > Ca2+ > Mg2+ > K+, respectively. Groundwater chemistry in the study area is mainly governed by rock dissolution and ion exchange. The dissolved minerals in groundwater mainly come from silicate weathering. The salinity of groundwater samples varies from ~1 to ~5%, and its source is possibly the paleo-brackish water which may be entrapped during past geologic periods.  相似文献   

8.
 Groundwater in alluvial aquifers of the Wakatipu and Wanaka basins, Central Otago, New Zealand, has a composition expressed in equivalent units of Ca2+≫Mg2+≅Na+>K+ for cations, and HCO3 –≫SO4 2->NO3 –≅Cl– for anions. Ca2+ and HCO3 – occur on a 1 : 1 equivalent basis and account for >80% of the ions in solution. However, some groundwater has increased proportions of Na+ and SO4 2-, reflecting a different source for this water. The rock material of the alluvial aquifers of both basins is derived from the erosion and weathering of metamorphic Otago Schist (grey and green schists). Calcite is an accessory mineral in both the grey and green schists at <5% of the rock. Geological mapping of both basins indicates that dissolution of calcite from the schist is the only likely mechanism for producing groundwater with such a constant composition dominated by Ca2+ and HCO3 – on a 1 : 1 equivalent basis. Groundwater with higher proportions of Na+ and SO4 2- occurs near areas where the schist crops out at the surface, and this groundwater represents deeper and possibly older water derived from basement fluids. Anomalously high K+ in the Wakatipu basin and high NO3 – concentrations in the Wanaka basin cannot be accounted for by interaction with basement lithologies, and these concentrations probably represent the influence of anthropogenic sources on groundwater composition. Received, June 1996 Revised, March 1997, July 1997 Accepted, July 1997  相似文献   

9.
In this study, the hydrochemical characteristics of shallow groundwater in a coastal region (Khulna) of southwest Bangladesh have been evaluated based on different indices for drinking and irrigation uses. Water samples were collected from 26 boreholes and analyzed for major cations and anions. Other physico-chemical parameters like pH, electrical conductivity (EC), and total dissolved solids were also measured. Most groundwater is slightly alkaline and largely varies in chemical composition, e.g. EC ranges from 962 to 9,370 μs/cm. The abundance of the major ions is as follows: Na+ > Ca2+ > Mg2+ > K+ = Cl− > HCO3 − > SO4 2− > NO3 −. Interpretation of analytical data shows two major hydrochemical facies (Na+–K+–Cl−–SO4 2− and Na+–K+–HCO3 −) in the study area. Salinity, 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. Results suggest that the brackish nature in most of the groundwaters is due to the seawater influence and hydrogeochemical processes.  相似文献   

10.
Hydrogeochemical assessment of groundwater in Moro area,Kwara state,Nigeria   总被引：1，自引：0，他引：1  
Detailed study of chemical analysis results of several groundwater samples (UNICEF-Assisted Water project, Kwara state, Nigeria) were carried out in an attempt to assess the quality and usability of groundwaters in the Moro area. Chemical analysis results indicate higher concentrations of Ca2+, Mg2+, and HCO3 – as compared to Na+, K+, Cl–, and SO4 2–. With exception of few locations where Fe is relatively higher, the concentrations of these ions together with other water quality parameters are all within permissible limits of the domestic and agricultural standards.On the basis of the analytical results, groundwaters in the study area are largely characterized as Ca-(Mg)-HCO3 type reflecting (possibly) young facies with limited migratory history. The occurrence of Ca-(Mg)-Na-HCO3 water type in certain areas is attributed to cation exchange processes. In addition, the observed scattered relationship between the TDS and the thickness of weathered horizons in the boreholes indicates the contribution of precipitation (recharge) to the ionic inputs in the groundwaters in addition to the weathering and dissolution processes.  相似文献   

11.
This paper reports original data on the physical and chemical parameters of precipitation, river water and groundwater in and around the Longhushan Nature Reserve Area, located in southwestern China karst region, and provides a preliminary characterization of the hydrogeochemical process governing the natural water evolution in this area. The rainfall and river water mainly pertain to the HCO3 −–Ca2+ type and groundwater mainly pertain to the HCO3 −–Ca2+ + Mg2+ type. The HCO3 − was the predominant anion and Ca2+ was the predominant cation in all waters, respectively. The Gibbs Boomerang Envelop model, the 1:1 relationship of Na+ plus K+ versus Cl− as well as the 1:1 relationship of Ca2+ plus Mg2+ versus HCO3 − all suggested geochemical weathering is the main controlling factor for the geochemical compositions of this natural water. In surface water, the Mg2+/Ca2+ ratios ranged from 0.32 to 0.42 and the Na+/Ca2+ varied between 0.04 and 0.05. In the groundwater, the Mg2+/Ca2+ ratios varied from 0.37 to 0.62 and were below the ideal ratio of 0.8. These ratios showed the presence of a dolomite source. Analysis of trace elements showed that As, B, Pb, Se, Sr, V and Zn elements were abundant in the natural water during summer in this region.  相似文献   

12.
An attempt has been made to study the groundwater geochemistry in part of the NOIDA metropolitan city and assessing the hydrogeochemical processes controlling the water composition and its suitability for drinking and irrigation uses. The analytical results show that Na and Ca are the major cations and HCO3 and Cl are the major anions in this water. The higher ratios of Na+K/TZ+ (0.2–0.7), Ca+Mg/HCO3 (0.8–6.1); good correlation between Ca-Mg (0.75), Ca-Na (0.77), Mg-Na (0.96); low ratio of Ca+Mg/Na+K (1.6), Ca/Na (1.03), Mg/Na (0.64), HCO3/Na (1.05) along with negative correlation of HCO3 with Ca and Mg signify silicate weathering with limited contribution from carbonate dissolution. The hydro-geochemical study of the area reveals that many parameters are exceeding the desirable limits and quality of the potable water has deteriorated to a large extent at many sites. High concentrations of TDS, Na, Cl, SO4, Fe, Mn, Pb and Ni indicate anthropogenic impact on groundwater quality and demand regional water quality investigation and integrated water management strategy. SAR, %Na, PI and Mg-hazard values show that water is of good to permissible quality and can be used for irrigation. However, higher salinity and boron concentration restrict its suitability for irrigation uses at many sites.  相似文献   

13.
Analyses of 72 samples from Upper Panjhara basin in the northern part of Deccan Plateau, India, indicate that geochemical incongruity of groundwater is largely a function of mineral composition of the basaltic lithology. Higher proportion of alkaline earth elements to total cations and HCO3>Cl + SO4 reflect weathering of primary silicates as chief source of ions. Inputs of Cl, SO4, and NO3 are related to rainfall and localized anthropogenic factors. Groundwater from recharge area representing Ca + Mg–HCO3 type progressively evolves to Ca + Na–HCO3 and Na–Ca–HCO3 class along flow direction replicates the role of cation exchange and precipitation processes. While the post-monsoon chemistry is controlled by silicate mineral dissolution + cation exchange reactions, pre-monsoon variability is attributable chiefly to precipitation reactions + anthropogenic factors. Positive correlations between Mg vs HCO3 and Ca + Mg vs HCO3 supports selective dissolution of olivine and pyroxene as dominant process in post-monsoon followed by dissolution of plagioclase feldspar and secondary carbonates. The pre-monsoon data however, points toward the dissolution of plagioclase and precipitation of CaCO3 supported by improved correlation coefficients between Na + Ca vs HCO3 and negative correlation of Ca vs HCO3, respectively. It is proposed that the eccentricity in the composition of groundwater from the Panjhara basin is a function of selective dissolution of olivine > pyroxene followed by plagioclase feldspar. The data suggest siallitization (L < R and R k) as dominant mechanism of chemical weathering of basalts, stimulating monosiallitic (kaolinite) and bisiallitic (montmorillonite) products. The chemical denudation rates for Panjhara basin worked out separately for the ground and surface water component range from 6.98 to 36.65 tons/km2/yr, respectively. The values of the CO2 consumption rates range between 0.18 × 106 mol//km2/yr (groundwater) and 0.9 × 106 mol/km2/yr (surface water), which indicates that the groundwater forms a considerable fraction of CO2 consumption, an inference, that is, not taken into contemplation in most of the studies.  相似文献   

14.
Hydrochemical investigations were carried out in Bahar area, Hamadan, western Iran, to assess the chemical composition of groundwater. The area falls in a semi-arid type of climate. In this area, groundwater has been exploited over the past century mainly for irrigation and water supply. A total of 135 representative groundwater samples were collected from different wells to monitor the water chemistry of various ions. Chemical analysis of the groundwater shows that the mean concentration of the cations is of the order Ca2+>Mg 2+>Na+>K+, while that for anions is SO42–>HCO3–>Cl–>NO3–. Statistical analyses indicate positive correlation between the following pairs of parameters Cl– and Mg 2+ (r=0.71), Cl– and Na+ (r=0.76), HCO3– and Na+ (r=0.56), SO42– and Mg2+ (r=0.76), SO42– and Na+ (r=0.69). Water presents a large spatial variability of the chemical facies (Ca-HCO3, Ca-SO4, Mg-HCO3, Mg-SO4, Na-HCO3) which is in relation to their interaction with the geological formations of the basin (carbonates, dolomite and various silicates) and evaporation. The hydrochemical types Ca-HCO3 and Ca-SO4 dominate the largest part of the studied area. The dissolution of halite, calcite, dolomite, and gypsum explains part of the contained Na +, Ca2+, Mg2+, Cl–, SO42– and HCO3–, but other processes, such as cation exchange and weathering of aluminosilicates also contribute to the water composition.  相似文献   

15.
This study was carried out to analyze groundwater quality in selected villages of Nalbari district, Assam, India, where groundwater is the main source of drinking water. 40 groundwater samples collected from hand pumps and analyzed for pH, EC, TDS, Ca2+, Mg2+, Na+, K+, HCO3 −, SO4 2−, Cl− and F−. Chemical analysis of the groundwater showed that mean concentration of cations in (mg/L) is in the order Ca2+ > Mg2+ > Na+ > K+ while for anions it is HCO3 − > Cl− > SO4 2− > F−. Fluoride concentration was recorded in the range of 0.02–1.56 mg/L. As per the desirable and maximum permissible limits for fluoride in drinking water recommended by WHO and by Bureau of Indian Standards (BIS), which is 1.5 mg/L, the groundwater of about 97% of the samples were found to be suitable for drinking purpose. The suitability of the groundwater for irrigation purpose was investigated by some determining factors such as sodium adsorption ratio, soluble sodium percentage, Kelly’s ratio and electrical conductivity. The value of the sodium absorption ratio and electrical conductivity of the groundwater samples were plotted in the US Salinity laboratory diagram for irrigation water. Most of the groundwater samples fall in the field of C2S1 and C3S1 indicating medium to high salinity and low sodium water, which can be used for irrigation on almost all types of soil with little doubt of exchangeable sodium. The hydrochemical facies shows that the groundwater is Ca-HCO3 type.  相似文献   

16.
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   

17.
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   

18.
An integrated study has been carried out to elucidate the distribution and occurrence of arsenic in selected groundwater samples in the area of Sherajdikhan, Bangladesh. Arsenic and other parameters (T, pH, EC, Na+, K+, Ca2+, Mg2+, Cl−, NO3 −, SO4 2−, HCO3 −, PO4 3−, Fe, Mn and DOC) have been measured in groundwater samples collected from shallow/deep tube wells at different depths. Hydrogeochemical data suggest that the groundwaters are generally Ca–Mg–HCO3 and Mg–Ca–HCO3 types with bicarbonate (HCO3 −) as the dominant anion, though the other type of water has also been observed. Dissolved arsenic in groundwater ranged from 0.006 to 0.461 mg/l, with 69% groundwater samples exceeded the Bangladesh limit for safe drinking water (0.05 mg/l). Correlation and principal component analysis have been performed to find out possible relationships among the examined parameters in groundwater. Low concentrations of NO3 − and SO4 2−, and high concentrations of DOC, HCO3 − and PO4 3− indicate the reducing condition of subsurface aquifer where sediments are deposited with abundant organic matter. Distinct relationship of As with Fe and Mn, and strong correlation with DOC suggests that the biodegradation of organic matter along with reductive dissolution of Fe–Mn oxyhydroxides has being considered the dominant process to release As in the aquifers studied herein.  相似文献   

19.
This study applied a comprehensive quantitative approach including statistical, principal component and gray relation analyses to assess the groundwater chemistry based on monitored data from 840 samples collected from the lower reaches of Tarim River from 2000 to 2009. The main findings were: (1) there were six types of groundwater chemistry in the lower reaches of Tarim River where Cl·SO4–Na·Mg was the dominant type accounting for 73.57% in all samples. There were linear relationships among chemical parameters, where TDS had significant multiple correlations with Na+, K+, Mg2+, Ca2+ and Cl−, respectively. (2) Three principal components (PC1, PC2 and PC3) were extracted. They included comprehensive measurements for salinization, alkalinity and pH, respectively. Most parameters showed decreasing trends during the period of 2000–2009, as well as the scores on PC1, because the concentrations of various chemical substances were diluted due to the uplift of the groundwater table in the lower reaches and the implementation of the ecological water delivery project in 2000. (3) HCO3 − was the most sensitive chemical parameter affected by the groundwater table followed by TA, Mg2+, TH, SO42−, K+, TDS and TS. PC2 was the most sensitive principal component to the change of the groundwater table followed by PC1 and PC3.  相似文献   

20.
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