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1.
High As contents in groundwater were found in Rayen area and chosen for a detailed hydrogeochemical study. A total of 121 groundwater samples were collected from existing tube wells in the study areas in January 2012 and analyzed. Hydrogeochemical data of samples suggested that the groundwater is mostly Na–Cl type; also nearly 25.62 % of samples have arsenic concentrations above WHO permissible value (10 μg/l) for drinking waters with maximum concentration of aqueous arsenic up to 25,000 μg/l. The reducing conditions prevailing in the area and high arsenic concentration correlated with high bicarbonate and pH. Results show that arsenic is released into groundwater by two major phenomena: (1) through reduction of arsenic-bearing iron oxides/oxyhydroxides and Fe may be precipitated as iron sulfide when anoxic conditions prevail in the aquifer sediments and (2) transferring of As into the water system during water–acidic volcanic rock interactions.  相似文献   

2.
Groundwater pollution by arsenic is a major health threat in suburban areas of Hanoi, Vietnam. The present study evaluates the effect of the sedimentary environments of the Pleistocene and Holocene deposits, and the recharge systems, on the groundwater arsenic pollution in Hanoi suburbs distant from the Red River. At two study sites (Linh Dam and Tai Mo communes), undisturbed soil cores identified a Pleistocene confined aquifer (PCA) and Holocene unconfined aquifer (HUA) as major aquifers, and Holocene estuarine and deltaic sediments as an aquitard layer between the two aquifers. The Holocene estuarine sediments (approximately 25–40 m depth, 9.6–4.8 cal ka BP) contained notably high concentrations of arsenic and organic matter, both likely to have been accumulated by mangroves during the Holocene sea-level highstand. The pore waters in these particular sediments exhibited elevated levels of arsenic and dissolved organic carbon. Arsenic in groundwater was higher in the PCA (25–94 μg/L) than in the HUA (5.2–42 μg/L), in both the monitoring wells and neighboring household tubewells. Elevated arsenic concentration in the PCA groundwater was likely due to vertical infiltration through the arsenic-rich and organic-matter-rich overlying Holocene estuarine sediments, caused by massive groundwater abstraction from the PCA. Countermeasures to prevent arsenic pollution of the PCA groundwater may include seeking alternative water resources, reducing water consumption, and/or appropriate choice of aquifers for groundwater supply.  相似文献   

3.
High arsenic levels in groundwater of the aquifers, belonging to the Pliocene terrestrial layers and Quaternary alluvial sediments, have become a significant problem for the inhabitants living in Sarkisla (Turkey). The main objective of this study was to determine the origin and arsenic contamination mechanisms of the Sarkisla drinking water aquifer systems. The highest arsenic concentrations were found in Pliocene layers and alluvial sediments with concentrations ranging from 2.1 to 155 mg/kg. These rocks are the main aquifers in the study area, and most of the drinking groundwater demand is met by these aquifers. Groundwater from the Pliocene aquifer is mainly Ca-HCO3 and Ca-SO4 water type with high EC values reaching up to 3,270 μS/cm, which is due to the sulfate dissolution in some parts of the alluvial aquifer. Stable isotope values showed that the groundwater was of meteoric origin. Tritium values for the groundwater were between 8.31 and 14.06 TU, representing a fast circulation in the aquifer. Arsenic concentrations in the aquifers were between 0.5 and 345 μg/L. The highest arsenic concentrations detected in the Pliocene aquifer system reached up to 345 μg/L with an average value of 60.38 μg/L. The arsenic concentrations of the wells were high, while the springs had lower arsenic concentrations. These springs are located in the upper parts of the study area where the rocks are less weathered. The hydrogeochemical properties demonstrated that the water–rock interaction processes in sulfide-bearing rocks were responsible for the remarkably high groundwater arsenic contamination in the study area. In the study area, the arsenic levels determined in groundwater exceeded the levels recommended by the WHO. Therefore, it is suggested that this water should not be used for drinking purposes and new water sources should be investigated.  相似文献   

4.
Arsenic in groundwaters of the alluvial aquifer of Bardsir plain, SE Iran   总被引：1，自引：1，他引：0  
Bardsir plain is located in the central part of Kerman Province of Iran. The relative prevalence of arsenic-related cancers, the high concentration of arsenic in nearby plains, as well as the recharge of this aquifer through the mountains composed of high-sulfide volcanic rocks have been motivations of the authors to study the concentration of this element in Bardsir plain. Arsenic concentration was measured in 63 groundwater samples using inductively coupled plasma mass spectrometry method. The results were evaluated through iso-concentration maps, correlation diagrams, and multivariate statistical methods. Accordingly, the concentration of arsenic ranges from 1.3 to 464.5 μg/l with an average value of 134.2 μg/l. So, the groundwaters are enriched with arsenic to much higher levels than permitted for than drinking water acceptable level (10 μg/l). The high arsenic levels in groundwaters of Bardsir plain are ascribed to joint influence of decomposition of sulfides present in mountainous volcanic rocks and the mixing with hydrothermal waters in some locations. Supposedly, the prevalence of higher than 8 pH values has enhanced the release of arsenic from Fe-hydroxides generated during sulfide weathering process.  相似文献   

5.
The stratigraphic and structural setting of the Cimini Mountains and Viterbo area of Italy has been reconstructed. The architecture of the tectonic edifice, below the Pleistocene Cimino and Vicano volcanic districts cover, is characterized by the Mesozoic–Cenozoic Tuscan Nappe and the similar Umbria-Marche Succession; both are capped by the overthrusted Ligurian Late Cretaceous–Eocene Tolfa Flysch. A shallow unconfined volcanic aquifer is separated, by a thick aquiclude, from the deep confined carbonate aquifer consisting of the Tuscan Nappe and the Umbria-Marche Succession. The volcanic aquifer hosts cold waters, whilst the carbonate aquifer hosts hot sulphate–alkaline earth waters that emerge in the thermal area of Viterbo with a temperature of 30–60°C. The recharge area of cold waters is located in the Cimini Mountains. Thermal waters of the Viterbo hot springs are derived from a circuit of waters that emerge along the River Nera near Narni (about 34 km ENE of Viterbo), with a high salinity, a temperature of 16–18°C, a sulphate–alkaline earth composition, and a discharge of 13 m3/sec, whose recharge area is located in the central pre-Apennines reliefs.  相似文献   

6.
A conceptual hydrogeological model of the Viterbo thermal area (central Italy) has been developed. Though numerous studies have been conducted on its geological, geochemical and geothermal features, there is no generalized picture defining the origin and yield of the hydrothermal system. These latter aspects have therefore become the objectives of this research, which is based on new hydrogeological and geochemical investigations. The geological setting results in the coexistence of overlapped interacting aquifers. The shallow volcanic aquifer, characterized by fresh waters, is fed from the area around the Cimini Mountains and is limited at its base by the semiconfining marly-calcareous-arenaceous complex and low-permeability clays. To the west of Viterbo, vertical upflows of thermal waters of the sulphate-chloride-alkaline-earth type with higher gas contents, are due to the locally uplifted carbonate reservoir, the reduced thickness of the semiconfining layer and the high local geothermal gradient. The hot waters (30–60°C) are the result of deep circulation within the carbonate rocks (0.5–1.8 km) and have the same recharge area as the volcanic aquifer. The upward flow in the Viterbo thermal area is at least 0.1 m3/s. This flow feeds springs and deep wells, also recharging the volcanic aquifer from below.  相似文献   

7.
A comparative hydrogeochemical study evaluated arsenic release mechanism and differences in contamination levels in the shallow groundwater of two areas within the deltaic environment of West Bengal (i.e. Karimpur and Tehatta blocks of Nadia district) in India. Groundwaters from both the areas are Ca-Na(K)-Cl-HCO3 type with highly reducing character (−110.16 ± 16.85 to −60.77 ± 16.93 mV). Low correlations among As, Fe, and Mn and the higher association between As and DOC are indicative of microbial decomposition of organic matter enhancing the weathering of shallow aquifer materials. Arsenic contamination in groundwater is higher in Karimpur (95 ± 81.17 μg/L) than that in Tehatta (43.05 ± 41.06 μg/L). The release mechanism of arsenic into groundwater is very complex. Low Fe (0.27–4.78 mg/L and 0.81–4.13 mg/L), Mn (0.08–0.2 mg/L and 0.03–0.22 mg/L), and SO42− (3.82 ± 0.31 and 2.78 ± 0.40 mg/L) suggest that the mechanism of arsenic release is not a single mechanistic pathway. Clustering of redox-active parameters in the principal component planes indicate that the reductive dissolution, and/or weathering/co-precipitation of Fe/Mn-bearing minerals in the shallow aquifer sediments control the dominant mechanistic pathway of arsenic release.  相似文献   

8.
This study investigates the origin and chemical composition of the thermal waters of Platystomo and Smokovo areas in Central Greece as well as any possible relationships of them to the neighboring geothermal fields located in the south-eastern part of Sperchios basin. The correlations between different dissolved salts and the temperature indicate that the chemical composition of thermal waters are controlled by, the mineral dissolution and the temperature, the reactions due to CO2 that originates possibly by diffusion from the geothermal fields of Sperchios basin and the mixing of thermal waters with fresh groundwater from karst or shallow aquifers. Two major groups of waters are recognized on the basis of their chemistry: thermal waters of Na–HCO3–Cl type and thermal waters mixed with fresh groundwater of Ca–Mg–Na–HCO3 type. All thermal waters of the study area are considered as modified by water–rock interaction rainwater, heated in depth and mixed in some cases with fresh groundwater when arriving to the surface. Trace elements present low concentrations. Lithium content suggests discrimination between the above two groups of waters. Boron geochemistry confirms all the above remarks. Boron concentration ranges from 60 μg L?1 to 10 mg L?1, while all samples’ constant isotopic composition (δ11B ≈ 10 ‰) indicates leaching from rocks. The positive correlation between the chemical elements and the temperature clearly indicates that much of the dissolved salts are derived from water–rock interactions. The application of geothermometers suggests that the reservoir temperature is around 100–110 °C. Chalcedony temperatures are similar to the emergent temperatures and this is typical of convective waters in fault systems in normal thermal gradient areas.  相似文献   

9.
Core sediments from three disturbed boreholes (JOR, GHAT, and RAJ) and two undisturbed boreholes (DW1 and DW2) were collected in the study area of the Chapai-Nawabganj district of northwestern Bangladesh for geochemical analyses. In the study area, groundwater samples from fourteen As-contained private wells and five nested piezometers at both the DW1 and DW2 boreholes were also collected and analyzed. The groundwater arsenic concentrations in the uppermost aquifer (10–40 m of depth) range from 3 to 315 μg/L (mean 47.73 ± 73.41 μg/L), while the arsenic content in sediments range from 2 to 14 mg/kg (mean 4.36 ± 3.34 mg/kg). An environmental scanning electron microscope (ESEM) with an energy dispersive X-ray spectrometer was used to investigate the presence of major and trace elements in the sediments. Groundwaters in the study area are generally the Ca–HCO3 type with high concentrations of As, but low levels of Fe, Mn, NO3 ? and SO 4 ?2 . The concentrations of As, Fe, Mn decrease with depth in the groundwater, showing vertical geochemical variations in the study area. Statistical analysis clearly shows that As is closely associated with Fe and Mn in the sediments of the JOR core (r = 0.87, p < 0.05 for Fe and r = 0.78, p < 0.05 for Mn) and GHAT core (r = 0.95, p < 0.05 for Fe and r = 0.93, p < 0.05 for Mn), while As is not correlated with Fe and Mn in groundwater. The comparatively low Fe and Mn concentrations in some groundwater and the ESEM image revealed that siderite precipitated as a secondary mineral on the surface of the sediment particles. The correlations along with results of sequential extraction experiments indicated that reductive dissolution of FeOOH and MnOOH represents a mechanism for releasing arsenic into the groundwater.  相似文献   

10.
Arsenic contamination of well water is a serious issue in the Nawalparasi District of the Terai region in Nepal. A local investigation was carried out on 137 tube wells in 24 communities of the district in December 2011. The investigation revealed that the average arsenic concentration in the tube wells was 350 μg/L, and that nearly 98 % of the wells exceeded the WHO guideline arsenic level limit of 10 μg/L. Highly contaminated well water, with more than 400 μg/L of arsenic, was found within the limited depth ranges of 18–22 and 50–80 m. High arsenic levels exceeding 500 μg/L were detected in shallower wells at Patkhauli, Mahuawa, Thulokunwar, and Goini located between 27.517° and 27.543°N and between 83.648° and 83.748°E. Boring sampling at five communities of Kashiya, Goini, Sanokunwar, Thulokunwar, and Mahuawa revealed two aquifers located at the two depths around 14–22 and 41–50 m in each community. Dark gray or black-colored peaty clay layers rich in organic matter were distributed at depths of 18–21 m beside the upper aquifers with high arsenic concentration in each community. Positive correlations were shown between iron and arsenic in the sediments from the five communities. It can be inferred that these results were caused by dissolution of iron-oxyhydroxide molecules with arsenic from solid phases. Microbial metabolisms have a great potential to induce the dissolution and release arsenic attached on the solid phases into aqueous phases depending on the level of redox potential and pH.  相似文献   

11.
Groundwater arsenic survey in Cachar and Karimganj districts of Barak Valley, Assam shows that people in these two districts are drinking arsenic-contaminated (max. 350 μg/l) groundwater. 66% of tubewells in these two districts have arsenic concentration above the WHO guideline value of 10 μg/l and 26% tubewells have arsenic above 50 μg/l, the Indian standards for arsenic in drinking water. 90% of installed tubewells in these two districts are shallow depth (14–40 m). Shallow tubewells were installed in Holocene Newer Alluvium aquifers are characterised by grey to black coloured fine grained organic rich argillaceous sediments and are mostly arsenic contamination in groundwater. Plio-Pleistocene Older Alluvium aquifers composed of shale, ferruginous sandstone, mottle clay, pebble and boulder beds, which at higher location or with thin cover of Newer Alluvium sediments are safe in arsenic contamination in groundwater. 91% of tubewell water samples show significantly higher concentrations of iron beyond its permissible limit of 1 mg/l. The iron content in these two districts varies from 0.5 to as much as 48 mg/l. Most of the arsenic contaminated villages of Cachar and Karimganj districts are located in entrenched channels and flood plains of Newer Alluvium sediments in Barak-Surma-Langai Rivers system. However, deeper tubewells (>60 m) in Plio-Pleistocene Older Alluvium aquifers would be a better option for arsenic-safe groundwater. The arsenic in groundwater is getting released from associated Holocene sediments which were likely deposited from the surrounding Tertiary Barail hill range.  相似文献   

12.
The occurrence of minor toxic elements (arsenic, vanadium and fluoride among others) in the volcanic aquifers of central Italy, with concentrations often above the national standards for drinking waters, has been recognized since the 1970s. However, these groundwaters are still often used for human consumption. With the aim of providing insight into the water–rock interaction processes, as well as into the evolution of arsenic and other elements, water-sampling campaigns where undertaken within a 100 km2 area at the eastern margin of the Viterbo region, where volcanites overlie an alluvial aquifer complex. The samples were analysed and geochemical modelling was applied to characterize the thermodynamic state of the waters. The results indicate the existence of direct relations among arsenic, vanadium and fluoride concentrations and of their inverse relationship with calcium concentration. An evolution scheme of groundwater composition from the upstream volcanic aquifer to the downstream sedimentary aquifer is also discussed. Two hypotheses are proposed which justify the observed decrease of the cited minor element concentrations, i.e. dilution processes and/or precipitation of fluorapatite, which can include in its structure small amounts of these elements. The precipitation hypothesis is supported by modelling results.  相似文献   

13.
This study addresses the hydrogeochemistry of thermal and cold waters from south east Tunisia. Temperature intervals are 38.5–68 °C and 22–27.8 °C for thermal water and cold water, respectively. Three distinct hydrogeological systems supply water either for irrigation or for drinking; they are: (1) the Continental Intercalaire geothermal aquifer (CI), (2) the Turonian aquifer and (3) the Senonian aquifer. A synthetic study including hydrochemical, hydrogeological and geothermal approaches have been applied in order to evaluate the inter-aquifers water transfer in south east of Tunisia. By using silica geothermometers and saturation indices for different solid phases, estimated thermal reservoir temperature varies between 52 and 87 °C and between 75 and 110 °C, respectively. Based on chemical and thermal data, mixing, which occurs between the ascending deep geothermal water and shallow cold water, is about 57 % cold water.  相似文献   

14.
Groundwater arsenic (As) concentrations above 10 μg/L (World Health Organization; WHO standard) are frequently found in the Titas Upazila in Bangladesh. This paper evaluates the groundwater chemistry and the mechanisms of As release acting in an underground aquifer in the middle-northeast part of the Titas Upazila in Bangladesh. Previous measurements and analyses of 43 groundwater samples from the region of interest (ROI) are used. Investigation is based on major ions and important trace elements, including total As and Fe in groundwater samples from shallow (8–36 m below ground level: mbgl) and deep (85–295 mbgl) tube wells in the aforementioned ROI. Principal hydrochemical facies are Ca–HCO3, with circumneutral pH. The different redox-sensitive constituents (e.g., As, Fe, Mn, NH4, and SO4) indicate overlapping redox zones, leading to differences regarding the redox equilibrium. Multivariate statistical analysis (factor analysis) was applied to reduce 20 chemical variables to four factors but still explain 81% of the total variance. The component loadings give hints as to the natural processes in the shallow aquifers, in which organic matter is a key reactant. The observed chemistry of As, Fe, and Mn can be explained by simultaneous equilibrium between Fe-oxide and SO4 reduction and an equilibrium of rhodochrosite precipitation/dissolution. A correlation test indicates the likeliness of As release by the reductive dissolution of Fe-oxides driven by the degradation of sediments organic matter. Other mechanisms could play a role in As release, albeit to a lesser extent. Reactive transport modeling using PHREEQC reproduced the observed chemistry evolution using simultaneous equilibrium between Fe-oxide and SO4 reduction and the equilibrium of rhodochrosite dissolution/precipitation alongside organic matter oxidation.  相似文献   

15.
Properties of geothermal resources in Kebilli region, Southwestern Tunisia   总被引：2，自引：2，他引：0  
The Kebilli region is located in the Southwestern part of Tunisia, and is characterized by the presence of deep and shallow geothermal systems (continental intercalary and complex terminal). Chemical and isotopic contents are used to classify the type and determine the origin of thermal water. An evaluation of reservoir temperature and a possible geothermal fluid mixing are also carried out. Both continental intercalary-deep aquifer and complex terminal-shallow aquifer are of Na–(Ca)–Cl–(SO4) mixed water type. The use of different geothermometers and the computation of saturation indexes for different solid phases suggests that the thermal reservoir temperature of the continental intercalary is between 92 and 105 °C, while the fluid temperature from the shallow complex terminal aquifer ranges from 50 to 75 °C. Also, the isotopic data indicates the old origin of all groundwater of Southwestern Tunisia. Mixing effects characterizing the continental intercalary and the complex terminal aquifers were identified using δ2H and δ18O relationship. It appears that the upward movement of thermal water from the deep aquifer to shallow ones is probably due to the abundant fractures in the research area.  相似文献   

16.
A heterogeneous anisotropic steady-state groundwater flow model for the multi-aquifer system of a part of southern Bengal Basin shows that human intervention has changed the natural groundwater flow system. At present, the shallow groundwater flow is restricted within the aquifer, with very short travel time of tens of years and vertical path length. The deep aquifer is fed by surface water or rainwater from distant locations with travel time of thousands of years and has no hydraulic connection with the arsenic-rich shallow aquifer. Numerical simulations indicate that the future pumping of deep groundwater is not likely to drive in arsenic from the shallow aquifer. Therefore, new wells may be installed in the deep aquifer. High pumping of shallow unpolluted aquifer consisting of brown sand will drive in groundwater containing organic matter from the post-Last Glacial Maximum aquifer-aquitard system. The organic matter drives reduction of manganese oxides at strip interfaces between palaeo-channel and palaeo-interfluve. After the completion of manganese reduction, FeOOH reduction may take place in the marginal palaeo-interfluvial aquifer and release sorbed arsenic. Arsenic then moves into the interior of palaeo-interfluvial aquifer polluting its fresh groundwater. Arsenic migration rates ranges between 0.21 and 6.3 and 1.3 × 10?2 and 0.4 m/year in horizontal and vertical directions, respectively. Therefore, palaeo-interfluvial aquifer will remain arsenic-free for hundreds to thousands of years to supply safe drinking water.  相似文献   

17.
This study observes groundwater hydrochemical characteristics during mixing between geothermal and non-geothermal fluids in Germencik–Nazilli area in the Büyük Menderes Basin (SW Turkey). Hydrogeochemical features of 32 non-geothermal, geothermal and surface samples were studied. The mean temperatures of the geothermal reservoirs are calculated to be 150–240 °C in Germencik field, based on Na-K-Mg geothermometry. Hydrochemical characteristics of Germencik geothermal fluid differ from non-geothermal fluids, mainly Na-Cl-HCO3-type geothermal fluid, while non-geothermal fluid is mostly Ca-Mg-HCO3-SO4 type. High contents of some minor elements in geothermal fluids are most likely sourced from prolonged water-rock interaction, reflecting the signals of flow paths and residence times. A mass-balance approach was used to calculate mixing ratios between geothermal and non-geothermal fluids based on B, Cl and Na concentrations. Germencik field is considerably characterised by rising geothermal fluids and overlying non-geothermal fluids. The amount of water stored in the Quaternary aquifer evolved from a deep thermal source is low in Germencik (.5–40% geothermal fluid in non-geothermal wells). Mixing between geothermal and non-geothermal fluids has been caused by groundwater utilisation practices and is increased close to active faults. Irrigation of the shallow groundwater composition is considered as influx of low-temperature geothermal fluid.  相似文献   

18.
《Applied Geochemistry》1997,12(4):411-427
Chemical and isotope compositions of fluid samples, collected between 1974 and 1986 from 52 springs or shallow boreholes located in the Mont-Dore region (Massif Central, France), were examined. Some springs and wells were sampled several times during this period. The fluids emerge from Quaternary volcanic rocks or Paleozoic granite at temperatures between 4 and 62°C, and the origin of the H2O is meteoric. The waters can be classified into three groups: bicarbonate fluids, mixed bicarbonate-chloride fluids (with a mineralization up to 8 g/l), and acid-sulfate fluids. Only two fluids contain sufficient Cl− to be considered as ‘mature’ waters. Previous work has demonstrated that they all contain partly mantle-derived CO2 gas, and that the CO2-rich gas phase and bicarbonate-chloride waters are separated at substantial depth.Mineralized fluids circulate at depth and undergo several processes, such as cooling or dilution with recent freshwater, during their ascent to the surface. Therefore, the CO2-rich gas phase can be partly dissolved in the freshwater, or in deep fluids after their dilution. This process leads to the dissolution of surrounding rocks; such dissolution is discussed on the basis of major-element concentrations (Na, K, Ca, Mg), as well as the Sr 87/86 isotope ratio. Dissolution of S-bearing minerals has also been demonstrated. The presence of the CO2-rich gas phase also leads to isotope exchange between CO2 and H2O. Some mineralized fluids are less affected by these processes than others, in which case they display the chemical and isotopic characteristics of the original deep fluids.It was shown that the applicability of geothermometer calculations for these waters is hampered by several processes that modify the chemical composition. However, some geothermometers can be used for estimating the temperature of the deep fluids using the chemical composition of the less modified fluids. They indicate that fluids emerging from volcanic rocks in the Dordogne valley reach temperatures of around 100–130°C at depth, while the temperature of the fluid that issues from the granite at Saint-Nectaire is 160–175°C at depth.  相似文献   

19.
Differences in the degree of confinement, redox conditions, and dissolved organic carbon (DOC) are the main factors that control the persistence of nitrate and pesticides in the Upper Floridan aquifer (UFA) and overlying surficial aquifer beneath two agricultural areas in the southeastern US. Groundwater samples were collected multiple times from 66 wells during 1993–2007 in a study area in southwestern Georgia (ACFB) and from 48 wells in 1997–98 and 2007–08 in a study area in South Carolina (SANT) as part of the US Geological Survey National Water-Quality Assessment Program. In the ACFB study area, where karst features are prevalent, elevated nitrate-N concentrations in the oxic unconfined UFA (median 2.5 mg/L) were significantly (p = 0.03) higher than those in the overlying oxic surficial aquifer (median 1.5 mg/L). Concentrations of atrazine and deethylatrazine (DEA; the most frequently detected pesticide and degradate) were higher in more recent groundwater samples from the ACFB study area than in samples collected prior to 2000. Conversely, in the SANT study area, nitrate-N concentrations in the UFA were mostly <0.06 mg/L, resulting from anoxic conditions and elevated DOC concentrations that favored denitrification. Although most parts of the partially confined UFA in the SANT study area were anoxic or had mixed redox conditions, water from 28 % of the sampled wells was oxic and had low DOC concentrations. Based on the groundwater age information, nitrate concentrations reflect historic fertilizer N usage in both the study areas, but with a lag time of about 15–20 years. Simulated responses to future management scenarios of fertilizer N inputs indicated that elevated nitrate-N concentrations would likely persist in oxic parts of the surficial aquifer and UFA for decades even with substantial decreases in fertilizer N inputs over the next 40 years.  相似文献   

20.

Background

High salinity and arsenic (As) concentrations in groundwater are widespread problems in the tidal deltaplain of southwest Bangladesh. To identify the sources of dissolved salts and As, groundwater samples from the regional shallow Holocene aquifer were collected from tubewells during the dry (May) and wet (October) seasons in 2012–2013. Thirteen drill cores were logged and 27 radiocarbon ages measured on wood fragments to characterize subsurface stratigraphy.

Results

Drill cuttings, exposures in pits and regional studies reveal a >5 m thick surface mud cap overlying a ~30 m thick upper unit of interbedded mud and fine sand layers, and a coarser lower unit up to 60 m thick dominated by clean sands, all with significant horizontal variation in bed continuity and thickness. This thick lower unit accreted at rates of ~2 cm/year through the early Holocene, with local subsidence or compaction rates of 1–3 mm/year. Most tubewells are screened at depths of 15–52 m in sediments deposited 8000–9000 YBP. Compositions of groundwater samples from tubewells show high spatial variability, suggesting limited mixing and low and spatially variable recharge rates and flow velocities. Groundwaters are Na–Cl type and predominantly sulfate-reducing, with specific conductivity (SpC) from 3 to 29 mS/cm, high dissolved organic carbon (DOC) 11–57 mg/L and As 2–258 ug/L, and low sulfur (S) 2–33 mg/L.

Conclusions

Groundwater compositions can be explained by burial of tidal channel water and subsequent reaction with dissolved organic matter, resulting in anoxia, hydrous ferric oxide (HFO) reduction, As mobilization, and sulfate (SO4) reduction and removal in the shallow aquifer. Introduction of labile organic carbon in the wet season as rice paddy fertilizer may also cause HFO reduction and As mobilization. Variable modern recharge occurred in areas where the clay cap pinches out or is breached by tidal channels, which would explain previously measured 14C groundwater ages being less than depositional ages. Of samples collected from the shallow aquifer, Bangladesh Government guidelines are exceeded in 46 % for As and 100 % for salinity.
  相似文献   

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