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1.
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   

2.
The present study investigates the hydrogeochemistry and contamination of Varamin deep aquifer located in the southeast of Tehran province, Iran. The study also evaluates groundwater suitability for irrigation uses. The hydrogeochemical study was conducted by collecting and analyzing 154 groundwater samples seasonally during 2014. Based on evolutionary sequence of Chebotarev, the aquifer is in the stage of SO4 + HCO3 in the north half of the plain and it has evolved into SO4 + Cl in the south half. The unusual increase in TDS and Cl? toward the western boundaries of the aquifer indicates some anomalies. These anomalies have originated from discharge of untreated wastewater of Tehran city in these areas. The studied aquifer contains four dominant groundwater types including Na–Ca–SO4 (55%), Na–Ca–HCO3 (22%), Na–Cl (13%) and Ca–Cl (10%). The spatial distributions of Na–Cl and Ca–Cl water types coincide with observed anomalies. Ionic relationships of SO4 2? versus Cl? and Na+ versus Cl? confirm that water–rock interaction and anthropogenic contribution are main sources of these ions in the groundwater. The main processes governing the chemistry of the groundwater are the dissolution of calcite, dolomite and gypsum along the flow path, and direct ion exchange. Reverse ion exchange controls the groundwater chemistry in the areas contaminated with untreated wastewater. Based on Na% and SAR, 10.3 and 27% of water samples are unsuitable for irrigation purposes, respectively. Regarding residual sodium carbonate, there is no treat for crop yields. Only 6% of water samples represent magnesium adsorption ratios more than 50% which are harmful and unsuitable for irrigation.  相似文献   

3.
Aquifer-based groundwater quality assessment offers critical insight into the major hydrochemical processes, and aids in making groundwater resources management decisions. The Texas Rolling Plains (TRP), spanning over 22 counties, is a major agro-ecological region in Texas from where highest groundwater nitrate (NO3 ?) levels in the state have been reported. In this study, we present a comparative assessment of major hydrochemical facies pertaining to NO3 ? contamination and a host of species such as sulfate (SO4 2?), chloride (Cl?), and total dissolved solids (TDS) in different water use classes in the Seymour and Blaine aquifers, underlying the TRP. Aquifer-stratified groundwater quality information from 1990 to 2010 was obtained from the Texas Water Development Board and aggregated over decadal scale. High groundwater salinization was found in the municipal water use class in the Blaine aquifer with about 100, 87 and 50 % of observations exceeding the secondary maximum contaminant level for TDS, SO4 2?, and Cl?, respectively in the 2000s (2000–2010). The NO3-contamination was more alarming in the Seymour aquifer with 82 and 61 % of observations, respectively, exceeding the maximum contaminant level (MCL) in the irrigation and municipal water use classes in the 2000s. Salinization was more influenced by SO4 2? and Cl? in the Blaine aquifer and by NO3 ? in the Seymour aquifer. High NO3 ? (>MCL) observations in the Seymour aquifer occurred in the Ca–HCO3 and Ca–Mg–HCO3 facies, the domains of fresh water recharge and anthropogenic influences (e.g., agricultural activities, waste disposal). High SO4 2?, Cl? and TDS observations in the Blaine aquifer dominated the Ca–Cl, Na–Cl, and mixed Ca(Mg)–SO4(Cl) facies indicating evaporite dissolution, mixing and solute exchange, and lack of fresh recharge.  相似文献   

4.
Correct identification of water inrush sources is particularly important to prevent and control mine water disasters. Hydrochemical analysis, Fisher discriminant analysis, and geothermal verification analysis were used to identify and verify the water sources of the multi‐aquifer groundwater system in Gubei coal mine, Anhui Province, North China. Results show that hydrochemical water types of the Cenozoic top aquifer included HCO3–Na+K–Ca, HCO3–Na+K–Mg and HCO3–Na+K, and this aquifer was easily distinguishable from other aquifers because of its low concentration of Na++K+ and Cl–. The Cenozoic middle and bottom aquifers, the Permian fissure aquifer, and the Taiyuan and Ordovician limestone aquifers were mainly characterized by the Cl–Na+K and SO4–Cl‐Na+K or HCO3–Cl–Na+K water types, and their hydrogeochemistries were similar. Therefore, water sources could not be identified via hydrochemical analysis. Fisher model was established based on the hydrogeochemical characteristics, and its discrimination rate was 89.19%. Fisher discrimination results were improved by combining them with the geothermal analysis results, and this combination increased the identification rate to 97.3 % and reasonably explained the reasons behind two water samples misjudgments. The methods described herein are also applicable to other mines with similar geological and hydrogeological conditions in North China.  相似文献   

5.
The Panama coastal aquifer system is an important water resource in the southeast coast of Sri Lanka that provides adequate supplies of water for agriculture and domestic uses. One of the biggest threats to these fragile aquifers is the sea water intrusion. In this study, recharging mechanism and geochemical evaluation of groundwater in the coastal sandy aquifer of Panama were evaluated using chemical and stable isotope techniques. Thirty groundwater samples were collected and analyzed for their major ion concentrations and stable isotope ratios of oxygen (18O/16O) and hydrogen (D/H). All studied samples showed a ranking of major anions in the order Cl? > HCO 3 ?  > SO 4 2?  > N-NO3 ? while cations showed a decreasing order of abundance with Na+ > Ca2+ > Mg2+ > K+. Dominant groundwater hydrogeochemical types were Na–Cl and mixed Ca–Mg–Cl. Results of saturation index calculations indicate that the investigated groundwater body was mostly saturated with respect to calcite, dolomite and gypsum. In addition, stable isotope and geochemical data suggest that fresh groundwater in the aquifer is recharged mainly by local precipitation with slight modification from evaporation and saline water intrusions. Isotope data suggest that mixing of salt water with freshwater occurs in aquifers which are located towards the lagoon. Since the communities in the study area depend entirely on groundwater, an understanding of the hydrogeochemical characteristics of the aquifer system is extremely important for the better water resource management in the region.  相似文献   

6.
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   

7.
Dar es Salaam Quaternary coastal aquifer is a major source of water supply in Dar es Salaam City used for domestic, agricultural, and industrial uses. However, groundwater overdraft and contamination are the major problems affecting the aquifer system. This study aims to define the principal hydrogeochemical processes controlling groundwater quality in the coastal strip of Dar es Salaam and to investigate whether the threats of seawater intrusion and pollution are influencing groundwater quality. Major cations and anions analysed in 134 groundwater samples reveal that groundwater is mainly affected by four factors: dissolution of calcite and dolomite, weathering of silicate minerals, seawater intrusion due to aquifer overexploitation, and nitrate pollution mainly caused by the use of pit latrines and septic tanks. High enrichment of Na+ and Cl? near the coast gives an indication of seawater intrusion into the aquifer as also supported from the Na–Cl signature on the Piper diagram. The boreholes close to the coast have much higher Na/Cl molar ratios than the boreholes located further inland. The dissolution of calcite and dolomite in recharge areas results in Ca–HCO3 and Ca–Mg–HCO3 groundwater types. Further along flow paths, Ca2+ and Na+ ion exchange causes groundwater evolution to Na–HCO3 type. From the PHREEQC simulation model, it appears that groundwater is undersaturated to slightly oversaturated with respect to the calcite and dolomite minerals. The results of this study provide important information required for the protection of the aquifer system.  相似文献   

8.
The present work was carried out in Nalbari district of Assam (India) with an objective to assess the quality of groundwater and to check its suitability for drinking and irrigation purposes. Groundwater samples were collected from 50 different locations during pre- and post-monsoon seasons of 2016. Results of chemical analysis revealed that mean concentration of cations varied in the order Ca2+?>?Na+?>?Mg2+?>?K+, while for anions the order was HCO3 ??>?Cl??>?SO42??>?NO32??>?F? during both pre- and post-monsoon seasons. The suitability of groundwater samples for drinking purpose was assessed by comparing the results of physico-chemical analysis of groundwater with Indian Standards. Further, its suitability for irrigation purpose was assessed by evaluating several parameters like sodium adsorption ratio (SAR), sodium percentage (Na%), magnesium ratio, Kelly’s ratio and residual sodium carbonate (RSC). The SAR values obtained for all the samples were plotted against EC values in the US Salinity Laboratory diagram, and it was revealed that the most of the samples fall under water type C2-S1 indicating medium salinity and low SAR. Further, it was found that the majority of the samples belong to Ca–Mg–HCO3 hydrochemical facies followed by Ca–Mg–Cl–SO4, whereas only a few samples belong to Na–K–HCO3 hydrochemical facies.  相似文献   

9.
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   

10.
We investigated major ions, stable isotopes, and radiocarbon dates in a Quaternary aquifer in semi-arid northwestern China to gain insights into groundwater recharge and evolution. Most deep and shallow groundwater in the Helan Mountains was fresh, with total dissolved solids <1,000 mg L?1 and Cl? <250 mg L?1. The relationships of major ions with Cl? suggest strong dissolution of evaporites. However, dissolution of carbonates, albite weathering, and ion exchange are also the major groundwater process in Jilantai basin. The shallow desert groundwater is enriched in δ18O and intercepts the local meteoric water line at δ18O = ?13.4 ‰, indicating that direct infiltration is a minor recharge source. The isotope compositions in intermediate confined aquifers resemble those of shallow unconfined groundwater, revealing that upward recharge from intermediate formations is a major source of shallow groundwater in the plains and desert. The estimated residence time of 10.0 kyr at one desert site, indicating that some replenishment of desert aquifers occurred in the late Pleistocene and early Holocene with a wetter and colder climate than at present.  相似文献   

11.
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   

12.
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   

13.
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   

14.
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   

15.
This work addresses hydrogeochemical processes in shallow aquifers, represented by the Quaternary alluvial deposits, from a part of the semi-arid Mexican Highlands through the evaluations of physicochemical parameters as well as the δ18O and δ2H compositions of groundwater. Mifflin diagram separates the Na-bicarbonate, sulphate and mixed groundwater into one group showing interactions with volcanic lithology in the recharge zones and another group interacting with the evaporite rich sedimentary formation. In the Gibbs diagram, the samples with Cl?/(Cl? + HCO3?) < 0.4 showed higher influence of ion exchange and the samples with Cl?/(Cl? + HCO3?) > 0.4 showed higher effects of evaporation. All of them were oversaturated with carbonate minerals (i.e., calcite and dolomite) and unsaturated with evaporites (i.e., gypsum and halite). Evaporation (earlier stage) occurred before the water-rock interactions (later stage). Evolution occurs through three different routes such as up to 7.5‰ enrichment in δ18O caused by the infiltration with a certain delay and subsequently, the water-rock interaction became dominant. Ternary mixing models revealed dominant influence of local recharge (C1) on the water system, contributing 70.4%. Water-rock interaction (C3) with 18% and evaporation (C2) with 11.6% had comparatively less influences. The presence of nitrate (2–60 mg/L) in the groundwater indicated variable degrees of anthropogenic pollution.  相似文献   

16.
Evaluation of major ion chemistry and solute acquisition process controlling water chemical composition were studied by collecting a total of fifty-one groundwater samples in shallow (<25 m) and deep aquifer (>25 m) in the Varanasi area. Hydrochemical facies, Mg-HCO3 dominated in the largest part of shallow groundwater followed by Na-HCO3 and Ca-HCO3 whereas Ca-HCO3 is dominated in deep groundwater followed by Mg-HCO3 and Na-HCO3. High As concentration (>50 μg/l) is found in some of the villages situated in northeastern parts (i.e. adjacent to the concave part of the meandering Ganga river) of the Varanasi area. Arsenic contamination is confined mostly in tube wells (hand pump) within the Holocene newer alluvium deposits, whereas older alluvial aquifers are having arsenic free groundwater. Geochemical modeling using WATEQ4F enabled prediction of saturation state of minerals and indicated dissolution and precipitation reactions occurring in groundwater. Majority of shallow and deep groundwater samples of the study area are oversaturated with carbonate bearing minerals and under-saturated with respect to sulfur and amorphous silica bearing minerals. Sluggish hydraulic conductivity in shallow aquifer results in higher mineralization of groundwater than in deep aquifer. But the major processes in deep aquifer are leakage of shallow aquifer followed by dominant ion-exchange and weathering of silicate minerals.  相似文献   

17.
High water demand for domestic use in Douala with over 3 million inhabitants is met mainly by shallow groundwater. Field measurements and water sampling in January 2015 were carried out to examine the major controls on the groundwater composition and spatial view of ions in the water, timing of recharge and link between the recharge process and quality of the water. Fifty-two water samples were analysed for major ions and stable hydrogen and oxygen isotopes. Low pH values (3.61–6.92) in the groundwater indicated an acidic aquifer; thus, prone to acidification. The dominant water type was Na–Cl. Nitrate, which exceeded the WHO guide value of 50 mg/l in 22% of the groundwater, poses a health problem. Mass ratios of Cl?/Br? in the water ranged from 54 to 3249 and scattered mostly along the mixing lines between dilute waters, septic-tank effluent and domestic sewage. A majority of the samples, especially the high NO3 ? shallow wells, clustered around the septic-tank effluent-end-member indicating high contamination by seepage from pit latrines; hence, vulnerable to pollution. Stable isotopes in the groundwater indicated its meteoric origin and rapid infiltration after rainfall. The δ18O values showed narrow ranges and overlaps in rivers, springs, open wells and boreholes. These observations depict hydraulic connectivity, good water mixing and a homogeneous aquifer system mainly receiving local direct uniform areal recharge from rainfall. The rapid and diffused recharge favours the leaching of effluent from the pit toilets into the aquifer; hence, the high NO3 ? and Cl? in shallow wells. Silicate weathering, ion exchange and leaching of waste from pit toilets are the dominant controls on the groundwater chemistry. Drilling of deep boreholes is highly recommended for good-quality water supply. However, due the hydraulic connection to the shallow aquifer, geochemical modelling of future effects of such an exploitation of the deeper aquifer should support groundwater management and be ahead of the field actions.  相似文献   

18.
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   

19.
El Shalal-Kema area is located east of Aswan town and Nile River. The Quaternary sediments (unconsolidated material of sands, gravels, and clays intercalation) represent the main aquifer in the studied area. Its water is under unconfined condition, and the water table is shallow (vary from 7.5 to 16.3 m). The concerned aquifer is recharged mainly from Aswan Dam Lake, from the excess irrigation water and from septic tanks, where the area is not served by sewage system. The direction of the groundwater movement is generally from south to north. The transmissivity values of the Quaternary aquifer (from three pumping tests) are relatively high (vary from 1,996 to 3,029 m2/day). The exploitation of groundwater is carried out where there is continuous withdrawal for industrial and domestic uses with a total average quantity of groundwater of 71,304 m3 per day (25.67 million m3 per year). The hydrochemical characteristics of the Quaternary aquifer is studied based on the chemical analysis of 29 groundwater and four surface water samples collected from different sites. The chemical composition of the groundwater is dominated by calcium Ca2+ from the cations and bicarbonate (HCO 3 ? ) from the anions, and the order of cation abundance is Ca2+ > Na+ > Mg2+ > K+ and HCO 3 ? > SO 4 2? > Cl? among the anions. The groundwater types are normal chloride water, normal sulfate water, and normal carbonate water. The hypothetical salt combination revealed the presence of different salts arranged in terms of their predominant as Ca(HCO3)2, Mg(HCO3)2, NaCl, Na2SO4, MgSO4, KCL, NaHCO3, MgCl2, CaSO4, and K2SO4. The analytical measurements to the NO2 and NH3 reveal that their values decrease in summer and increase in winter due to the stoppage of pumping which leads to the increase of the wastewater quantities that reach the groundwater. The chemical and microbiological analyses show that the aquifer in this area is contaminated with fecal and disease-causing bacteria. The main cause of this contamination is the outflow from the septic tanks; therefore, the construction of sewage network is a vital solution. Chlorination is important to disinfect the groundwater at the tanks before its distribution to the houses.  相似文献   

20.
Exploration of unconventional natural gas reservoirs such as impermeable shale basins through the use of horizontal drilling and hydraulic fracturing has changed the energy landscape in the USA providing a vast new energy source. The accelerated production of natural gas has triggered a debate concerning the safety and possible environmental impacts of these operations. This study investigates one of the critical aspects of the environmental effects; the possible degradation of water quality in shallow aquifers overlying producing shale formations. The geochemistry of domestic groundwater wells was investigated in aquifers overlying the Fayetteville Shale in north-central Arkansas, where approximately 4000 wells have been drilled since 2004 to extract unconventional natural gas. Monitoring was performed on 127 drinking water wells and the geochemistry of major ions, trace metals, CH4 gas content and its C isotopes (δ13CCH4), and select isotope tracers (δ11B, 87Sr/86Sr, δ2H, δ18O, δ13CDIC) compared to the composition of flowback-water samples directly from Fayetteville Shale gas wells. Dissolved CH4 was detected in 63% of the drinking-water wells (32 of 51 samples), but only six wells exceeded concentrations of 0.5 mg CH4/L. The δ13CCH4 of dissolved CH4 ranged from −42.3‰ to −74.7‰, with the most negative values characteristic of a biogenic source also associated with the highest observed CH4 concentrations, with a possible minor contribution of trace amounts of thermogenic CH4. The majority of these values are distinct from the reported thermogenic composition of the Fayetteville Shale gas (δ13CCH4 = −35.4‰ to −41.9‰). Based on major element chemistry, four shallow groundwater types were identified: (1) low (<100 mg/L) total dissolved solids (TDS), (2) TDS > 100 mg/L and Ca–HCO3 dominated, (3) TDS > 100 mg/L and Na–HCO3 dominated, and (4) slightly saline groundwater with TDS > 100 mg/L and Cl > 20 mg/L with elevated Br/Cl ratios (>0.001). The Sr (87Sr/86Sr = 0.7097–0.7166), C (δ13CDIC = −21.3‰ to −4.7‰), and B (δ11B = 3.9–32.9‰) isotopes clearly reflect water–rock interactions within the aquifer rocks, while the stable O and H isotopic composition mimics the local meteoric water composition. Overall, there was a geochemical gradient from low-mineralized recharge water to more evolved Ca–HCO3, and higher-mineralized Na–HCO3 composition generated by a combination of carbonate dissolution, silicate weathering, and reverse base-exchange reactions. The chemical and isotopic compositions of the bulk shallow groundwater samples were distinct from the Na–Cl type Fayetteville flowback/produced waters (TDS ∼10,000–20,000 mg/L). Yet, the high Br/Cl variations in a small subset of saline shallow groundwater suggest that they were derived from dilution of saline water similar to the brine in the Fayetteville Shale. Nonetheless, no spatial relationship was found between CH4 and salinity occurrences in shallow drinking water wells with proximity to shale-gas drilling sites. The integration of multiple geochemical and isotopic proxies shows no direct evidence of contamination in shallow drinking-water aquifers associated with natural gas extraction from the Fayetteville Shale.  相似文献   

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