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1.
The Koyna River basin in India drew the attention of geoscientists after an earthquake (magnitude 7) in 1967. Since then, detailed geological, tectonic, and seismic investigations of this river basin have been carried out by several workers. However, very little study has been done on its hydrogeological framework. The present work aims at filling this gap. Basalts, laterites, alluvium, soils, and talus deposits form shallow unconfined aquifers, with transmissivity of 27–135 m2/d and a regional specific yield of 0.012. In shallow basaltic aquifers, the lower part of the highly weathered and highly jointed horizon above, and the poorly weathered and highly jointed horizon below, form the most potential zone for groundwater occurrence. Well yields in the deeper basaltic aquifers are directly related to the occurrence of lineaments, whereas at a shallower level they are related to geomorphic features. Spring discharges are highly dependent on their source aquifers and areas of recharge. They have a mean winter discharge of 46 m3/d and a summer discharge of 28 m3/d. Chemically, groundwaters are dominated by alkaline earths (Ca2+, Mg2+) and weak acids (HCO3 –, CO3 –); they are calcium-bicarbonate type (53%) and calcium-magnesium-bicarbonate type (27%) at shallower levels; and calcium-magnesium-bicarbonate type (29%), sodium-bicarbonate type (24%), calcium-bicarbonate type (19%), and calcium-magnesium-sodium-bicarbonate type (19%) in deeper aquifers. The Koyna River basin is characterized by both scarcity and abundance of groundwater. In the water-scarce areas in the dissected plateaus, artificial recharge of aquifers through construction of several recharge structures at suitable locations is highly recommended. In the water-abundant areas in the central valley, on the other hand, expanded consumptive use of water resources is encouraged. Electronic Publication  相似文献   

2.
Hydrogeochemical investigations are carried out in the northeastern part of Nagpur urban to assess the quality of groundwater for its suitability for drinking and irrigation purposes. Groundwater samples are collected from both shallow and deep aquifers to monitor the hydrochemistry of various ions. The groundwater quality of the area is adversely affected by urbanization as indicated by distribution of EC and nitrate. In the groundwater of study area, Ca2+ is the most dominant cation and Cl− and HCO3 − are the dominant anions. Majority of the samples have total dissolved solids values above desirable limit and most of them belong to very hard type. As compared to deep aquifers, shallow aquifer groundwaters are more polluted and have high concentration of NO3 −. The analytical results reveal that most of the samples containing high nitrate also have high chloride. Major hydrochemical facies were identified using Piper trilinear diagram. Alkaline earth exceeds alkalis and weak acids exceed strong acids. Shoeller index values reveal that base-exchange reaction exists all over the area. Based on US salinity diagram most of samples belong to high salinity-low sodium type. A comparison of groundwater quality in relation to drinking water standards showed that most of the water samples are not suitable for drinking purpose.  相似文献   

3.
 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   

4.
Datong Basin is one of the Cenozoic faulted basins in Northern China’s Shanxi province, where groundwater is the major source of water supply. The results of hydrochemical investigation show that along the groundwater flow path, from the margins to the lower-lying central parts of the basin, groundwater generally shows increases in concentrations of TDS, HCO3 ?, SO4 2?, Cl?, Na+ and Mg2+ (except for Ca2+ content). Along the basin margin, groundwater is dominantly of Ca–HCO3 type; however, in the central parts of the basin it becomes more saline with Na–HCO3-dominant or mixed-ion type. The medium-deep groundwater has chemical compositions similar to those of shallow groundwater, except for the local area affected by human activity. From the mountain front to the basin area, shallow groundwater concentrations of major ions increase and are commonly higher than those in medium-deep aquifers, due to intense evapotranspiration and anthropogenic contamination. Hydrolysis of aluminosilicate and silicate minerals, cation exchange and evaporation are prevailing geochemical processes occurring in the aquifers at Datong Basin. The isotopic compositions indicate that meteoric water is the main source of groundwater recharge. Evaporation is the major way of discharge of shallow groundwater. The groundwater in medium-deep aquifers may be related to regional recharges of rainwater by infiltrating along the mountain front faults, and of groundwater permeating laterally from bedrocks of the mountain range. However, in areas of groundwater depression cones, groundwater in the deep confined aquifers may be recharged by groundwater from the upper unconfined aquifer through aquitards.  相似文献   

5.
Degradation of groundwater quality by human activities is a widespread environmental problem in Vietnam. Groundwater there is a major source of water for domestic and industrial purposes. This paper reviews, compiles, and comprehensively analyzes spatiotemporal variations of hydrological and hydrogeological characteristics of shallow and deep groundwater aquifers in northern Hanoi industrial zones and in nearby Red River water. Groundwater level, electrical conductivity, and water temperature were measured in six monitoring wells, complemented by anion, cation, and stable isotope analyses of ground and surface water. The results show that the groundwater in both shallow and deep aquifers was fresh, but mainly calcium-bicarbonate type contaminants and human activities affect groundwater and surface water composition. With the goal of devising sustainable water use regulations, more research must be directed toward long-term monitoring of groundwater and surface water quality, as well as toward detailed investigation of the hydraulic characteristics of local aquifers in the study area.  相似文献   

6.
Groundwater constitutes the main source of water supply in the High Mekerra watershed of northwestern Algeria. This resource is currently under heavy pressures to meet the growing needs of drinking water and irrigation. This study assesses the geochemical characteristics of groundwater of the High Mekerra watershed at 21 points distributed across the two main aquifers (Ras El Ma and Mouley Slissen) in the region. Hydrochemical facies of Ras El Ma groundwater are dominantly MgCl and CaCl type, while those of Mouley Slissen groundwater are of CaHCO3 type. Principal component analysis shows a strong correlation between groundwater mineralization and Ca2+, Na+, Cl? and SO4 2? ions stemming from the dissolution of carbonates, gypsum and anhydrite. Groundwater mineralization evolves from south to north. Geochemical modeling shows that the High Mekerra groundwater is saturated with respect to calcite and dolomite and undersaturated with respect to gypsum and anhydrite. Nitrate concentrations that exceed the WHO standard (50 mg L?1) at several points are linked to the agro-pastoral activities in this region.  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.
The Ganges River water and riverbank shallow groundwater were studied during a single wet season using the hydrochemical and isotopic composition of its dissolved load. The dissolved concentrations of major ions (Cl?, SO4 2?, NO3 ?, HCO3 ?, Ca2+, Na+, Mg2+, and K+), trace elements (barium (Ba) and strontium (Sr)) and stable isotopes (O and D) were determined on samples collected from the Ganges River and its riverbank shallow aquifers. In the present study, the shallow groundwater differs significantly from the Ganges River water; it shows distinct high concentrations of Ca2+, Mg2+, HCO3 ?, Ba, and Sr due to water–rock interaction and this in particular suggests that the Ganges River may not contribute significantly to the riverbank shallow aquifers during wet season. Besides, the sum of the total cationic charge (∑+, in milliequivalents per liter) in the groundwater shows high values (2.48 to 13.91 meq/L, average 9.12 meq/L), which is much higher than the sum of the cations observed in the Ganges water (1.36 to 3.10 meq/L, average 1.94 meq/L). Finally, the more depleted stable isotopic (δ 18O and δ 2H) compositions of the Ganges River water are in contrast to those of the riverbank aquifer having enriched stable isotopic values during the wet season and the riverbank groundwater thus has a purely local origin from precipitation.  相似文献   

9.
Continual expansion of population density, urbanization, agriculture, and industry in most parts of the world has increased the generation of pollution, which contributes to the deterioration of surface water quality. This causes the dependence on groundwater sources for their daily needs to accumulate day by day, which raises concerns about their quality and hydrogeochemistry. This study was carried out to increase understanding of the geological setup and assess the groundwater hydrogeochemical characteristics of the multilayered aquifers in Lower Kelantan Basin. Based on lithological data correlation of exploration wells, the study area can be divided into three main aquifers: shallow, intermediate and deep aquifers. From these three aquifers, 101 groundwater samples were collected and analyzed for various parameters. The results showed that pH values in the shallow, intermediate and deep aquifers were generally acidic to slightly alkaline. The sequences of major cations and anions were Na+ > Ca2+ > Mg2+ > K+ and HCO3? > Cl? > SO42? > CO32?, respectively. In the intermediate aquifer, the influence of ancient seawater was the primary factor that contributed to the elevated values of electrical conductivity (EC), Cl? and total dissolved solids (TDS). The main facies in the shallow aquifer were Ca–HCO3 and Na–HCO3 water types. The water types were dominated by Na–Cl and Na–HCO3 in the intermediate aquifer and by Na–HCO3 in the deep aquifer. The Gibbs diagram reveals that the majority of groundwater samples belonged to the deep aquifer and fell in the rock dominance zone. Shallow aquifer samples mostly fell in the rainfall zone, suggesting that this aquifer is affected by anthropogenic activities. In contrast, the results suggest that the deep aquifer is heavily influenced by natural processes.  相似文献   

10.
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   

11.
《Applied Geochemistry》2004,19(2):231-243
In large parts of rural Argentina people depend on groundwater whose As content exceeds the Argentine drinking water standards (0.05 mg l−1). The most affected areas are located in the Chaco-Pampean Plain, where aquifers comprise Tertiary loess deposits (in the Pampean Plain) and Tertiary and Quaternary fluvial and aeolian sediments (in the Chaco Plain). Robles county is located in the alluvial cone of the Dulce River consisting of loess (aeolian), and gravel, silt, sand and clay (alluvial) deposits. In the shallow aquifers, more than 48% of the 63 studied wells show As at toxic levels (maximum 4.8 mg l−1), while in the deep groundwater the concentration is below 0.05 mg l−1. The pH of the shallow groundwaters range between 6.5 and 9 and generally have high electrical conductivity with mean values of 2072 and 1693 μS/cm−1 in the years 1998 and 1999, respectively. Arsenic concentrations are high in the alkaline Na–HCO3 type groundwaters, where As correlates positively with Na+ and HCO3−. Moreover, As correlates positively with Mo, U, and V, while a negative correlation was observed with Ca2+ and Mg2+. The potential sources of groundwater As are: (i) layers of volcanic ash with 90% of rhyolitic glass; (ii) volcanic glass dispersed in the sediments; and (iii) clastic sediments of metamorphic and igneous origin. Great lateral variability in the concentration of groundwater As is caused by several hydrogeological and hydrogeochemical factors.  相似文献   

12.
Groundwater is the most important source of water supply in Iran and understanding the geochemical evolution of groundwater is important for sustainable development of the water resources in Tabas area. A total of 29 samples of groundwater in Tabas area have been analyzed for ions and major elements. Groundwater of the study area is characterized by the dominance of Na–Cl water type. Groundwater was generally acidic to high alkaline with pH ranging from 5.42 to 10.75. The TDS as a function of mineralization characteristics of the groundwater ranged from 479 to 10,957 mg/l, with a mean value of 2,759 mg/l. The Ca2+, Mg2+, SO4 2? and HCO3 ? were mainly derived from the dissolution of calcite, dolomite and gypsum. The Cu, Pb and Zn ions are not mobile in recent pH–Eh, but these conditions controlled dissolved Se, V and Mo in groundwater. The As is released in groundwater as a result of the weathering of sulfide minerals like arsenopyrite.  相似文献   

13.
Study on geochemistry of groundwater occurring at different depths is rarely attempted due to inherent difficulties in sample isolation and lack of significant species variations. Three-dimensional (spatial, temporal and depth-wise) evaluation of water chemistry variations would give holistic picture of aquatic chemistry. In order to fill the knowledge gap the vertical hydrogeochemistry of Penna-Chitravati inter-stream sub-basin is studied.Water samples are segregated into different groups based on water levels of source wells. The group samples pertaining to granite terrain (A to C) does not show much variation for tested parameters as most of the samples fall within 20m water level. In shale aquifers groundwater is progressively less ionized as depth to levels increases (Group D to G). Reduction of EC and Na-Cl along with falling water levels indicates deeper aquifers are free from contamination. Gradual decrease in HCO 3 - with depth substantiates that deeper aquifers are getting less fresh water due to lack of inter connectivity in shale formations. Sodium in groundwater of both the granite and shale aquifers is contributed by weathering of silicate rocks as the Na+/Cl- molar ratio is >1 in many samples. Majority of the samples in both the geological terrains have Ca2+/Mg2+ ratio between 1 to < 2 indicating dolomite dissolution is responsible for Ca2+-Mg2+ contribution. The chemistry of tested water indicate aquifer matrix is responsible for chemical make-up of pore water which was obliterated due to extraneous sources like anthropogenic contamination as Na+, Cl-, NO 3 - and SO 4 2- /HCO 3 - is high in many samples belonging to shallow aquifers. Thermodynamic action in deep aquifers could be responsible for dissimilar water chemistry in aquifers belonging to same geological domain.  相似文献   

14.
Water resources are a key factor, particularly for the planning of the sustainable regional development of agriculture, as well as for socio-economic development in general. A hydrochemical investigation was conducted in the Friuli Venezia Giulia aquifer systems to identify groundwater evolution, recharge and extent of pollution. Temperature, pH, electric conductivity, total dissolved solids, alkalinity, total hardness, SAR, Ca2+, Na+, K+, Mg2+, Cl−, SO4 2−, NO3 −, HCO3 − , water quality and type, saturation indexes and the environmental stable isotope δ18O were determined in 149 sampling stations. The pattern of geochemical and oxygen stable isotope variations suggests that the sub-surface groundwater (from phreatic and shallow confined aquifers) is being recharged by modern precipitations and local river infiltrations. Four hydrogeological provinces have been recognised and mapped in the Friuli Venezia Giulia Plain having similar geochemical signatures. These provinces have different degrees of vulnerability to contamination. The deep confined groundwater samples are significantly less impacted by surface activities; and it appears that these important water resources have very low recharge rates and would, therefore, be severely impacted by overabstraction.  相似文献   

15.
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   

16.
In the salinity affected lower Atrai floodplain aquifer in the NW Bangladesh, geoelectric resistivity survey and hydrochemical analysis are carried out with an aim to identify fresh and saline groundwater zones; investigate the status of salinity; evaluate hydrochemical processes involved and suggest management approaches for irrigation. Here a two-fold aquifer system, inter-layered by silt, clay and silty-clay aquitard and aquiclude is classified as: upper aquifer — spatially affected by salinity of varying degrees; and lower aquifer — generally characterized by high salinity. The aquifer with resistivity values greater than 69 Ωm is safe for irrigation use. Concentrations of major ions vary as: Ca2+>Na+>Mg2+>K+ and HCO3>Cl>NO3>SO4 2?. Groundwater is dominated by Na-Ca to Ca-Na, HCO3-Cl-SO4, Cl-SO4-HCO3 and Cl-SO4 2? facies where Ca2+, Mg2+, SO4 2?, HCO3 ?, Cl? and NO3 2? ion concentrations are statistically dominant and water is of Ca-Mg, HCO3-SO4-Cl and NO3 types. Geochemically, groundwater is hard and saline to fresh water type. Salinity increases with depth, but spatially towards the southern part. Groundwater quality is a product of water-rock interaction, direct mixing and marine spraying, or fall-out of airborne marine salts, where silicate weathering is the primary source of bivalent cations. Sediment provenance of alkaline earth silicates and higher concentrations of alkalis are derived from sources other than precipitation. In general partially or fully salinity affected upper and lower aquifers in the area except in its eastern part are not suitable for tubewell irrigation. As groundwater demand for irrigation is increasing, the saline water has progressively invaded relatively fresher parts of the aquifer by upconning. So, special salinity control management approaches can be adopted through engineering techniques such as groundwater abstraction optimization, as also through scientific behavioral approaches like groundwater demand management, salt tolerant crops production. In this context, surface water conservation and rain water harvesting for domestic and irrigational uses are recommended in the salinity affected area.  相似文献   

17.
The alluvial aquifer of the Alto Guadalquivir River is one of the most important shallow aquifers in Jaén, Spain. It is located in the central-eastern part of the province, and its groundwater resources are used mainly for crop irrigation in an agriculture-dominated area. Hydrochemical and water-quality data obtained through a 2-year sampling (2004–2006) and analysis program indicate that nitrate pollution is a serious problem affecting groundwater due to the use of nitrogen (N)-fertilizers in agriculture. During the study, 231 water samples were collected from wells and springs to determine water chemistry and the extent of nitrate pollution. The concentration of nitrate in groundwater ranged from 1.25 to 320.88 mg/l. Considerable seasonal fluctuations in groundwater quality were observed as a consequence of agricultural practices and other factors such as annual rainfall distribution and the Guadalquivir River flow regime. The chemical composition of the water is not only influenced by agricultural practices, but also by interaction with the alluvial sediments. The dissolution of evaporites accounts for part of the Na+, K+, Cl−, SO4 2−, Mg2+, and Ca2+, but other processes, such as calcite precipitation and dedolomitization, also contribute to groundwater chemistry.  相似文献   

18.
Concentration and isotope ratios (δ34SSO4 and δ18OSO4) of dissolved sulfate of groundwater were analyzed in a very large anaerobic aquifer system under the Lower Central Plain (LCP) (25,000 km2) in Thailand. Groundwater samples were collected in two different kinds of aquifers; type 1 with a saline water contribution and type 2 lateritic aquifers with no saline water contribution. Two different isotopic compositional trends were observed: in type 1 aquifers sulfate isotope ratios range from low values (+2.2‰ for δ34SSO4 and +8.0‰ for δ18OSO4) to high values (+49.9‰ for δ34SSO4 and +17.9‰ for δ18OSO4); in type 2 aquifers sulfate isotope ratios range from low values (−0.1‰ for δ34SSO4 and +12.2‰ for δ18OSO4) to high δ18OSO4 ratios (+18.4‰) but with low δ34SSO4 ratios (<+12.9‰). Isotopic comparison with possible source materials and theoretical geochemical models suggests that the sulfate isotope variation for type 1 aquifer groundwater can be explained by two main processes. One is the contribution of remnant seawater, which has experienced dissimilatory sulfate reduction in the marine clay, into recharge water of freshwater origin. This process accounts for the high salinity groundwater. The other process, explaining for the modest salinity groundwater, is the bacterial sulfate reduction of the mixture water between high salinity water and fresh groundwater. Isotopic variation of type 2 aquifer groundwater may also be explained by bacterial sulfate reduction, with slower reduction rate than that of the groundwater with saline water effect. The origin of groundwater sulfate with low δ34SSO4 but high δ18OSO4 is recognized as an important topic to be examined in a future investigation.  相似文献   

19.
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   

20.
Sediment and groundwater profiles were compared in two villages of Bangladesh to understand the geochemical and hydrogeological factors that regulate dissolved As concentrations in groundwater. In both villages, fine-grained sediment layers separate shallow aquifers (< 28 m) high in As from deeper aquifers (40-90 m) containing < 10 μg/L As. In one village (Dari), radiocarbon dating indicates deposition of the deeper aquifer sediments > 50 ka ago and a groundwater age of thousands of years. In the other village (Bay), the sediment is < 20 ka old down to 90 m and the deeper aquifer groundwater is younger, on the order of hundreds of years. The shallow aquifers in both villages that are high in As contain bomb-3H and bomb-14C, indicating recent recharge. The major and minor ion compositions of the shallow and deeper aquifers also differ significantly. Deeper aquifer water is of the Na+-HCO3- type, with relatively little dissolved NH4+ (76 ± 192 μmol/L), Fe (27 ± 43 μmol/L) and Mn (3 ± 2 μmol/L). In contrast, shallow aquifer water is of the Ca2+-Mg2+-HCO3- type, with elevated concentrations of dissolved NH4+ (306 ± 355 μmol/L), Fe (191 ± 73 μmol/L), and Mn (27 ± 43 μmol/L). In both villages, the quantity of As extractable from deeper aquifer sands with a 1 mol/L phosphate solution (0.2 ± 0.3 mg/kg, n = 12; 0.1 ± 0.1 mg/kg, n = 5) is 1 order of magnitude lower than P-extractable As from shallow deposits (1.7 ± 1.2 mg/kg, n = 9; 1.4 ± 2.0 mg/kg, n = 11). The differences suggest that the concentration of P-extractable As in the sediment is a factor controlling the concentration of As in groundwater. Low P-extractable As levels are observed in both deeper aquifers that are low in As, even though there is a large difference in the time of deposition of these aquifers in the two villages. The geochemical data and hydrographs presented in this study suggest that both Holocene and Pleistocene deeper aquifers that are low in As should be a viable source of drinking water as long as withdrawals do not exceed recharge rates of ∼1 cm/yr.  相似文献   

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