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1.
Investigations were undertaken in the riparian zone near Shangba village, an AMD area, in southern China to determine the effects that river–groundwater interactions and groundwater residence time have had on environmental quality and geochemical evolution of groundwater. Based on the Darcy’s law and ionic mass balances as well as the method of isotopic tracer, the results showed that there were active interactions between AMD-contaminated river water and groundwater in the riparian zone in the study area. River water was found to be the main source of groundwater recharge in the northwestern part of the study area, whereas groundwater was found to be discharging into the river in the southeastern part of the study area throughout the year. End-member mixing analysis quantified that the contributions of river water to groundwater decreased gradually from 35.9% to negligible levels along the flow path. The calculated mixing concentrations of major ions indicated that water–rock reactions were the most important influence on groundwater quality. The wide range of Ca2+?+?Mg2+ and HCO3? ratios and the change of groundwater type from Ca2+–SO42? type to a chemical composition dominated by Ca2+–HCO3? type indicated a change of the major water–rock reaction process from the influence of H2SO4 (AMD) to that of CO2 (soil respiration) along a groundwater flow path. Furthermore, the kinetics interpretation of SO42? and HCO3? concentrations suggested that the overlapping time of their kinetics triggered the hydrochemical evolution and the change of major weathering agent. This process might take approximately 8 years and this kinetic time will be continued when a steady source of contamination enter the aquifer.  相似文献   

2.
The functional factors responsible for fluoride (F?)-bearing groundwater used for drinking as well as for cooking in the area of Gummanampadu Sub-basin, Guntur District, Andhra Pradesh, India are discussed. The study area is a part of an Archean Gneissic Complex, consisting of banded-biotite-hornblende-gneisses, over which the Proterozoic Cumbhum quartzites, shales, phyllites, and dolomitic limestones occur. The chemistry of groundwater is dominated by carbonates (HCO3 ? and CO3 2?) at a higher pH. This results in a higher total alkalinity over total hardness, causing an excess alkalinity. Sodium ion is dominated among the cations (Ca2+, Mg2+, and K+). The concentration of F? (2.1–3.7 mg/L) is higher than that of desirable national limit (1.2 mg/L) prescribed for drinking purpose. A significant positive correlation exists between F? and pH as well as that between F? and HCO3 ? + CO3 2?. This indicates that the alkaline condition is the prime conducive factor for dissolving F?-bearing minerals more effectively leading to a higher concentration of F? in the groundwater. Furthermore, a positive chloro-alkaline index reflects the ion exchange, and an oversaturation with respect to CaCO3 indicates the evaporation. In addition, a negative relation between the well depth and F? shows the effect of solubility and/or leaching of salts in different depth levels. These factors regulate the concentration of F? in the groundwater. On the other hand, a positive correlation of F? with SO4 2? as well as with K+ shows the human land use activities (namely, use of chemical fertilizers, disposal of domestic wastes, etc.), which add F? to the groundwater. A significant number of the residents of the study area suffer from the health disorders related to fluorosis, which is a consequence of higher concentration of F? in the drinking water. Thus, this study emphasizes the need for supply of safe drinking water, nutritional diet, rainwater-harvesting structures, and public education to realize “health for all” motto of World Health Organization.  相似文献   

3.
In a mid-continental North American grassland, solute concentrations in shallow, limestone-hosted groundwater and adjacent surface water cycle annually and have increased steadily over the 15-year study period, 1991-2005, inclusive. Modeled groundwater CO2, verified by measurements of recent samples, increased from 10−2.05 atm to 10−1.94 atm, about a 20% increase, from 1991 to 2005. The measured groundwater alkalinity and alkaline-earth element concentrations also increased over that time period. We propose that carbonate minerals dissolve in response to lowered pH that occurs during an annual carbonate-mineral saturation cycle. The cycle starts with low saturation during late summer and autumn when dissolved CO2 is high. As dissolved CO2 decreases in the spring and early summer, carbonates become oversaturated, but oversaturation does not exceed the threshold for precipitation. We propose that groundwater is a CO2 sink through weathering of limestone: soil-generated CO2 is transformed to alkalinity through dissolution of calcite or dolomite. The annual cycle and long-term increase in shallow groundwater CO2 is similar to, but greater than, atmospheric CO2.  相似文献   

4.
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   

5.
In this study, it is determined physicochemical properties of the groundwater and the spatial variability of physicochemical properties of the groundwater in the Amik plain and as well as assess its suitability for drinking and irrigation. A total 92 groundwater samples were collected from drilled well in June 2012. In addition, the 42 of 92 drilled wells were also sampled in September 2012 to evaluate the changes of groundwater properties. According to t test values, the mean Ca2+, SO4 2?, Mg2+ and TH values in the June period were significantly lower than those of the September period. On the other hand, the mean (CO 3 2?  + HCO3 ?) and RSC and MR values in the June period were significantly higher than those of the September period. The order of relative abundance of major cations in the groundwater (in mg L?1) is in order Na+ > Mg2+ > Ca2+ > K+. The order of the anions abundance (mg L?1) is SO4 2? > Cl? > HCO3 ? > CO3 2? in this research. Log and square-root transformation were carried out for the most of the water properties before the calculation of semivariance. The nugget ratio showed all the variables were strongly spatial dependent except for K+ and Mg2+ and (CO3 2? + HCO3 ?) which showed moderate spatial dependence (ratio ranging from 28 to 49.9 %). Spatial distribution analysis of groundwater quality indicated that The EC, TDS values and Na and Cl? contents which is important water quality parameters increase from northern towards southern. The total hardness values increase also from northwestern towards southwestern.  相似文献   

6.
MIS 11 is often considered to be the best climatic analogue for the Holocene. Many studies have suggested, however, that it is a period of extreme climate warmth comparable in temperatures to the Middle and Late Pliocene. In Britain deposits of the Hoxnian interglacial are correlated to MIS 11 and multi-proxy techniques can be used to reconstruct the climate of this interglacial. Soil, groundwater and freshwater carbonates are common in Hoxnian deposits and the stable isotopic composition of these precipitates can be used to increase our understanding of MIS 11 environments in Britain. Carbonates from Marks Tey, Clacton, Swanscombe, Elveden and West Stow are studied, the stratigraphic context of which indicates that their formation is broadly synchronous (in the mid-Hoxnian, pollen zones Ho II to Ho III). The carbon isotopic composition of groundwater and pedogenic carbonates is typically depleted with respect to δ13C (ca −9 to −8‰ VPDB) reflecting uptake of plant respired CO2 during water migration/recharge. The carbon isotopic composition of lacustrine carbonate is more enriched with respect to δ13C (ca 0-1‰VPDB) reflecting the equilibration of lake waters with atmospheric CO2. The δ18O of groundwater and pedogenic carbonates is slightly more enriched than modern soil carbonates but not as enriched as soil carbonates formed under interglacials that were warmer than the Holocene (i.e. the Cromerian). The stable isotopic composition of Hoxnian carbonates does not, therefore, indicate that this interglacial was characterised by uniquely warm climates in the context of other Middle Pleistocene interglacials and the Holocene. This is contrary to many marine and littoral records from around the world but consistent with environmental records from Britain and Europe.  相似文献   

7.
Geochemical processes that take place in the aquifer have played a major role in spatial and temporal variations of groundwater quality. This study was carried out with an objective of identifying the hydrogeochemical processes that controls the groundwater quality in a weathered hard rock aquifer in a part of Nalgonda district, Andhra Pradesh, India. Groundwater samples were collected from 45 wells once every 2 months from March 2008 to September 2009. Chemical parameters of groundwater such as groundwater level, EC and pH were measured insitu. The major ion concentrations such as Ca2+, Mg2+, Na+, K+, Cl−, and SO4 2− were analyzed using ion chromatograph. CO3 − and HCO3 − concentration was determined by acid–base titration. The abundance of major cation concentration in groundwater is as Na+ > Ca2+ > Mg2+ > K+ while that of anions is HCO3 − > SO4 2− > Cl− > CO3 −. Ca–HCO3, Na–Cl, Ca–Na–HCO3 and Ca–Mg–Cl are the dominant groundwater types in this area. Relation between temporal variation in groundwater level and saturation index of minerals reveals the evaporation process. The ion-exchange process controls the concentration of ions such as calcium, magnesium and sodium. The ionic ratio of Ca/Mg explains the contribution of calcite and dolomite to groundwater. In general, the geochemical processes and temporal variation of groundwater in this area are influenced by evaporation processes, ion exchange and dissolution of minerals.  相似文献   

8.
An approach is presented to investigate the regional evolution of groundwater in the basin of the Amacuzac River in Central Mexico. The approach is based on groundwater flow cross-sectional modeling in combination with major ion chemistry and geochemical modeling, complemented with principal component and cluster analyses. The hydrogeologic units composing the basin, which combine aquifers and aquitards both in granular, fractured and karstic rocks, were represented in sections parallel to the regional groundwater flow. Steady-state cross-section numerical simulations aided in the conceptualization of the groundwater flow system through the basin and permitted estimation of bulk hydraulic conductivity values, recharge rates and residence times. Forty-five water locations (springs, groundwater wells and rivers) were sampled throughout the basin for chemical analysis of major ions. The modeled gravity-driven groundwater flow system satisfactorily reproduced field observations, whereas the main geochemical processes of groundwater in the basin are associated to the order and reactions in which the igneous and sedimentary rocks are encountered along the groundwater flow. Recharge water in the volcanic and volcano-sedimentary aquifers increases the concentration of HCO3 –, Mg2+ and Ca2+ from dissolution of plagioclase and olivine. Deeper groundwater flow encounters carbonate rocks, under closed CO2 conditions, and dissolves calcite and dolomite. When groundwater encounters gypsum lenses in the shallow Balsas Group or the deeper Huitzuco anhydrite, gypsum dissolution produces proportional increased concentration of Ca2+ and SO4 2–; two samples reflected the influence of hydrothermal fluids and probably halite dissolution. These geochemical trends are consistent with the principal component and cluster analyses.  相似文献   

9.
Groundwater survey has been carried out in the area of Gummanampadu sub-basin located in Guntur District, Andhra Pradesh, India for assessing the factors that are responsible for changing of groundwater chemistry and consequent deterioration of groundwater quality, where the groundwater is a prime source for drinking and irrigation due to non-availability of surface water in time. The area is underlain by the Archaean Gneissic Complex, over which the Proterozoic Cumbhum rocks occur. The results of the plotting of Ca2+ + Mg2+ versus HCO3 ? + CO3 2?, Ca2+ + Mg2+ versus total cations, Na+ + K+ versus total cations, Cl? + SO4 2? versus Na+ + K+, Na+ versus Cl?, Na+ versus HCO3 ? + CO3 2?, Na+ versus Ca2+ and Na+: Cl? versus EC indicate that the rock–water interaction under alkaline condition is the main mechanism in activating mineral dissociation and dissolution, causing the release of Ca2+, Mg2+, Na+, K+, HCO3 ?, CO3 2?, SO4 2? and F? ions into the groundwater. The ionic relations also suggest that the higher concentrations of Na+ and Cl? ions are the results of ion exchange and evaporation. The influences of anthropogenic sources are the other cause for increasing of Mg2+, Na+, Cl?, SO4 2? and NO3 ? ions. Further, the excess alkaline condition in water accelerates more effective dissolution of F?-bearing minerals. Moreover, the chemical data plotted in the Piper’s, Gibbs’s and Langelier–Ludwig’s diagrams, computed for the chloro-alkaline and saturation indices, and analyzed in the principal component analysis, support the above hypothesis. The groundwater quality is, thus, characterized by Na+ > Ca2+ > Mg2+ > K+: HCO3 ? + CO3 2? > Cl? > SO4 2? > NO3 ? > F? facies. On the other hand, majority of groundwater samples are not suitable for drinking with reference to the concentrations of TDS, TH, Mg2+ and F?, while those are not good for irrigation with respect to USSL’s and Wilcox’s diagrams, residual sodium carbonate, and magnesium hazard, but they are safe for irrigation with respect to permeability index. Thus, the study recommends suitable management measures to improve health conditions as well as to increase agricultural output.  相似文献   

10.
Hydrochemistry of groundwater in Chithar Basin, Tamil Nadu, India was used to assess the quality of groundwater for determining its suitability for drinking and agricultural purposes. Physical and chemical parameters of groundwater such as electrical conductivity, pH, total dissolved solids (TDS), Na+, K+, Ca2+, Mg2+, Cl–, HCO3–, CO32–, SO42–, NO–3, F–, B– and SiO2 were determined. Concentrations of the chemical constituents in groundwater vary spatially and temporarily. Interpretation of analytical data shows that mixed Ca–Mg–Cl, Ca–Cl and Na–Cl are the dominant hydrochemical facies in the study area. Alkali earths (Ca2+, Mg2+) and strong acids (Cl–, SO42–) are slightly dominating over alkalis (Na+, K+) and weak acids (HCO3–, CO32–). The abundance of the major ions is as follows: Na+ Ca2+ Mg2+ > K+ = Cl– > HCO3–> SO42– > NO3– > CO32– . Groundwater in the area is generally hard, fresh to brackish, high to very high saline and low alkaline in nature. High total hardness and TDS in a few places identify the unsuitability of groundwater for drinking and irrigation. Such areas require special care to provide adequate drainage and introduce alternative salt tolerance cropping. Fluoride and boron are within the permissible limits for human consumption and crops as per the international standards.  相似文献   

11.
A holistic study of the composition of the basalt groundwaters of the Atherton Tablelands region in Queensland, Australia was undertaken to elucidate possible mechanisms for the evolution of these very low salinity, silica- and bicarbonate-rich groundwaters. It is proposed that aluminosilicate mineral weathering is the major contributing process to the overall composition of the basalt groundwaters. The groundwaters approach equilibrium with respect to the primary minerals with increasing pH and are mostly in equilibrium with the major secondary minerals (kaolinite and smectite), and other secondary phases such as goethite, hematite, and gibbsite, which are common accessory minerals in the Atherton basalts. The mineralogy of the basalt rocks, which has been examined using X-ray diffraction and whole rock geochemistry methods, supports the proposed model for the hydrogeochemical evolution of these groundwaters: precipitation + CO2 (atmospheric + soil) + pyroxene + feldspars + olivine yields H4SiO4, HCO3 −, Mg2+, Na+, Ca2+ + kaolinite and smectite clays + amorphous or crystalline silica + accessory minerals (hematite, goethite, gibbsite, carbonates, zeolites, and pyrite). The variations in the mineralogical content of these basalts also provide insights into the controls on groundwater storage and movement in this aquifer system. The fresh and weathered vesicular basalts are considered to be important in terms of zones of groundwater occurrence, while the fractures in the massive basalt are important pathways for groundwater movement.  相似文献   

12.
Cave dripwater hydrochemistry responds to environmental changes, both within and outside of the cave, and thereby conveys this information to any stalagmite fed by the drips. As stalagmites are important archives of climate proxy information, understanding how dripwater hydrochemistry responds to environmental forcing is critical. However, despite the large number of speleothems in SW China, the response of dripwater to regional climate variability is not yet adequately understood. A 3‐year study of three drip sites in Xueyu Cave, Chongqing Municipality, SW China, revealed the most important mechanisms controlling dripwater chemical variability. The principal chemical indices (pH, specific conductivity, Ca2+, Mg2+, Sr2+ and ) in collected dripwaters and the local climate data were analysed in this study. The principal controls on the hydrochemistry were found to be the external climate and its changes, groundwater residence time, cave ventilation and prior calcite precipitation (PCP) processes. Dripwater hydrochemistry showed strongly coherent seasonal patterns despite the fact that all sites are Ca–HCO3 type waters and supersaturated with calcite. Seasonal changes in dripwater hydrochemistry were influenced by the soil and vadose zone CO2 content as well as groundwater residence time in the upper karst zone. Cave‐air CO2 seasonal variations were consistent with changes in dripwater PCO2 and cave ventilation. Trace element ratios (Mg/Ca and Sr/Ca) of dripwater were controlled by PCP processes. Seasonal variations in dripwater Mg/Ca and Sr/Ca ratios in Xueyu Cave showed inverse changes with the Asia Monsoon Index during the monitoring period, reflecting the seasonal climate changes that may have been recorded in the speleothems. Based on a linear regression of PCO2 and the Ca2+ data in the cold–dry winter season, a 130‐ppm shift in cave‐air PCO2 results in a 1‐ppm shift in dripwater Ca2+ concentration in Xueyu Cave. This study illustrates the importance of understanding factors controlling the changes in the composition of dripwater before it reaches the speleothem.  相似文献   

13.
The objective of this study was to identify geochemical processes and Quaternary geological events responsible for the variations in groundwater geochemistry observed in a sedimentary rock aquifer system, including brackish to saline groundwater. Inorganic constituents and environmental isotopes were analyzed for 146 groundwater samples. Dissolution of carbonates dominates in recharge areas, resulting in Ca-, Mg-HCO3 groundwater. Further along flow paths, under confined conditions, Ca2+–Na+ ion exchange causes groundwater evolution to Na-HCO3 type. Na-Cl groundwater is also found and it falls on a seawater mixing line. Using conservative tracers, Cl− and Br−, the original Champlain Sea water is shown to have been, in the region, a mixture of about 34% seawater and 66% freshwater, a composition still retained by some groundwater. Na-Cl groundwater thus results from mixing with former Champlain Sea water and also from solute diffusion from overlying marine clay. The system is thus found to be at different stages of desalinization, from the original Champlain Sea water still present in hydraulically stagnant areas of the aquifer to fully flushed conditions in parts, where more flow occurs, especially in recharge zones. The geochemical processes are integrated within the hydrogeological context to produce a conceptual geochemical evolution model for groundwater of the aquifer system.  相似文献   

14.
An investigation of the thermal waters in the Ústí nad Labem area in the northeastern part of the Eger Rift has been carried out, with the principal objective of determining their origin. Waters from geothermal reservoirs in the aquifers of the Bohemian Cretaceous Basin (BCB) from depths of 240 to 616 m are exploited here. For comparison, thermal waters of the adjacent Teplice Spa area were also incorporated into the study. Results based on water chemistry and isotopes indicate mixing of groundwater from aquifers of the BCB with groundwater derived from underlying crystalline rocks of the Erzgebirge Mts. Unlike thermal waters in Dě?ín, which are of Ca–HCO3 type, there are two types of thermal waters in Ústí nad Labem, Na–HCO3–Cl–SO4 type with high TDS values and Na–Ca–HCO3–SO4 type with low TDS values. Carbon isotope data, speciation calculations, and inverse geochemical modeling suggest a significant input of endogenous CO2 at Ústí nad Labem in the case of high TDS groundwaters. Besides CO2 input, both silicate dissolution and cation exchange coupled with dissolution of carbonates may explain the origin of high TDS thermal waters equally well. This is a consequence of similar δ13C and 14C values in endogenous CO2 and carbonates (both sources have 14C of 0 pmc, endogenous CO2 δ13C around −3‰, carbonates in the range from −5‰ to +3‰ V-PDB). The source of Cl− seems to be relict brine formed in Tertiary lakes, which infiltrated into the deep rift zone and is being flushed out. The difference between high and low TDS groundwaters in Ústí nad Labem is caused by location of the high mineralization groundwater wells in CO2 emanation centers linked to channel-like conduits. This results in high dissolution rates of minerals and in different δ13C(DIC) and 14C(DIC) fingerprints. A combined δ34S and δ18O study of dissolved SO4 indicates multiple SO4 sources, involving SO4 from relict brines and oxidation of H2S. The study clearly demonstrates potential problems encountered at sites with multiple sources of C, where several evolutionary groundwater scenarios are possible.  相似文献   

15.
Geoelectrical resistivity method involving vertical electrical sounding (VES) was carried out in a sedimentary environment to determine the suitability of the method for sub-surface groundwater investigations. The EC and TDS hydrochemical data in the study area clearly showed the influence of seawater intrusion. The abundance of the major cations and anions are in the following order, Na+ > Ca2+ > Mg 2+ > K+ = Cl- > HCO3- > SO42- > CO3 > NO3 > PO4. Results suggest that the groundwater in this study area is very hard and alkaline in nature. As indicated by Piper trilinear diagram, NaCl and Ca2+ - Mg2+–Cl- - SO42- facies are the dominant hydrochemical facies in the groundwater of Pearl city. The VES method by Schlamberger electrode array was applied in 12 locations, which is expected to represent the whole area. The resistivity meter (aquameter CRM 5OO) was used to collect the VES data by employing a Schlumberger electrode configuration, with half current electrode spacing (AB/2) ranging from 2 to 180 m and the potential electrode (MN) from 1 to 50 m. The resistivity data is then interpreted by WINSEV 1-D inversion program geoelectric software to entirely describe the aquifer system as well as the occurrence of groundwater. The outputs of sub-surface layers with resistivities and thickness presented in contour maps and 2-D views by using SURFER software were created. Accordingly, three zones with different resistivity values were detected, corresponding to three different formations: (1) a transition zone of sandy soil (aeolian deposits) thick formation, (2) strata’s saturated with fresh groundwater in the east disturbed by the presence of sandy shell limestone horizons, (3) a water-bearing formation in the west containing low saltwater horizons. The bedrock is encountered at an average depth of 95m. This study indicates that the groundwater reservoirs are mainly confined to the alluvial aquifer.  相似文献   

16.
The change in groundwater chemistry along the groundwater flow path in the Matsumoto tunnel vicinity was studied, and the origin of the groundwater and dissoluted substances was determined. The relationship between the concentration of HCO3 –, Ca2+, and Na+, and CO2 gas pressure in the groundwater indicated that the HCO3 –, Ca2+, and Na+ were produced by the reaction of the CO2 gas in the groundwater and feldspar in the rocks. The relationship between the concentration of NO3 – and the Eh and pH values in the groundwater indicated that in an oxidative condition, ammonia-oxidizing and nitriteoxidizing bacteria used NH4 + and produced NO3 – and H+, and in a reductive condition, denitrifying bacteria used NO3 – and produced N2 gas and OH–. The stable hydrogen and oxygen isotopic ratio in the groundwater and precipitation indicated that the groundwater originated from precipitation that had fallen on the area. The concentration of3H and the stable hydrogen and oxygen isotopic ratios in the groundwater suggested that it has been getting warmer climatically for more than 60 years. The stable carbon isotopic ratio indicated that the HCO3 – in the groundwater, excluding deep well water, originated from CO2 gas produced by organic matter in the soil. The deep well water, which had a higher concentration of HCO3 – than the other groundwater sampled, was thought to have acquired HCO3 – though contact with rocks. The36Cl/Cl ratio indicated the recharge age of the deep well water sampled at a depth of 760 m at the foot of the plateau was recent.  相似文献   

17.
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   

18.
Recent studies of uranium(VI) geochemistry have focused on the potentially important role of the aqueous species, CaUO2(CO3)32− and Ca2UO2(CO3)30(aq), on inhibition of microbial reduction and uranium(VI) aqueous speciation in contaminated groundwater. However, to our knowledge, there have been no direct studies of the effects of these species on U(VI) adsorption by mineral phases. The sorption of U(VI) on quartz and ferrihydrite was investigated in NaNO3 solutions equilibrated with either ambient air (430 ppm CO2) or 2% CO2 in the presence of 0, 1.8, or 8.9 mM Ca2+. Under conditions where the Ca2UO2(CO3)30(aq) species predominates U(VI) aqueous speciation, the presence of Ca in solution lowered U(VI) adsorption on quartz from 77% in the absence of Ca to 42% and 10% at Ca concentrations of 1.8 and 8.9 mM, respectively. U(VI) adsorption to ferrihydrite decreased from 83% in the absence of Ca to 57% in the presence of 1.8 mM Ca. Surface complexation model predictions that included the formation constant for aqueous Ca2UO2(CO3)30(aq) accurately simulated the effect of Ca2+ on U(VI) sorption onto quartz and ferrihydrite within the thermodynamic uncertainty of the stability constant value. This study confirms that Ca2+ can have a significant impact on the aqueous speciation of U(VI), and consequently, on the sorption and mobility of U(VI) in aquifers.  相似文献   

19.
The potential for metal release associated with CO2 leakage from underground storage formations into shallow aquifers is an important consideration in assessment of risk associated with CO2 sequestration. Metal release can be driven by acidification of groundwaters caused by dissolution of CO2 and subsequent dissociation of carbonic acid. Thus, acidity is considered one of the main drivers for water quality degradation when evaluating potential impacts of CO2 leakage. Dissolution of carbonate minerals buffers the increased acidity. Thus, it is generally thought that carbonate aquifers will be less impacted by CO2 leakage than non-carbonate aquifers due to their high buffering potential. However, dissolution of carbonate minerals can also release trace metals, often present as impurities in the carbonate crystal structure, into solution. The impact of the release of trace metals through this mechanism on water quality remains relatively unknown. In a previous study we demonstrated that calcite dissolution contributed more metal release into solution than sulfide dissolution or desorption when limestone samples were dissolved in elevated CO2 conditions. The study presented in this paper expanded our work to dolomite formations and details a thorough investigation on the role of mineral composition and mechanisms on trace element release in the presence of CO2. Detailed characterization of samples from dolomite formations demonstrated stronger associations of metal releases with dissolution of carbonate mineral phases relative to sulfide minerals or surface sorption sites. Aqueous concentrations of Sr2+, CO2+, Mn2+, Ni2+, Tl+, and Zn2+ increased when these dolomite rocks were exposed to elevated concentrations of CO2. The aqueous concentrations of these metals correlate to aqueous concentrations of Ca2+ throughout the experiments. All of the experimental evidence points to carbonate minerals as the dominant source of metals from these dolomite rocks to solution under experimental CO2 leakage conditions. Aqueous concentrations of Ca2+ and Mg2+ predicted from numerical simulation of kinetic dolomite dissolution match those observed in the experiments when the surface area is three to five orders of magnitude lower than the surface area of the samples measured by gas adsorption.  相似文献   

20.
The dissolution behavior of natural, ordered kutnahorite (Mn1.14Ca0.82Mg0.04Fe0.012(CO3)2) and a disordered, calcian rhodochrosite (Mn1.16Ca0.78Mg0.06(CO3)2) precipitated in the laboratory was investigated in deionized distilled water and artificial seawater in both open and closed systems at 25 °C, one atmosphere total pressure, and various pCO2s. Both solids dissolved congruently in distilled water in an open system and yielded identical long-term equilibration or extrapolated ion activity products, IAPpkt = aCa 2+aMn 2+(aCO 3 2?)2 = 1.7 (±0.12)× 10?21 or pIAPpkt = 20.77 (±0.03). This value is believed to be the thermodynamic solubility product of pseudokutnahorite. In contrast, the steady state ion concentration products, ICPpkt = [Ca2+][Mn2+][CO3 2?]2, measured following the dissolution of both minerals in artificial seawater increase as the CO2 partial pressure decreases and the [Mn2+]:[Ca2+] ratio increases. These observations are interpreted as resulting from the formation of phases of different stoichiometry in response to large variations of the [Mn2+]:[Ca2+] ratio in solution. These data and results of calcite-seawater equilibration experiments in the presence of various dissolved Mn(II) concentrations define the fields of stability of manganoan calcites and calcian rhodochrosites in seawater within Lippmann phase diagrams for the CaCO3–MnCO3–H2O system. Results of this study reveal that the nature (i.e., mineralogy) and composition of manganese-rich carbonate phases that may form under suboxic/anoxic conditions in marine sediments are dictated by the porewater [Mn2+]:[Ca2+] ratio, the abundance of calcite surfaces and reaction kinetics.  相似文献   

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