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1.
Water management in semiarid and arid catchments such as the Poopó Lake Basin requires improved understanding of the complex behavior of the various contaminants, which affect the drinking water quality and considered as crucial for sustainable development of the region. Mechanisms of arsenic (As) release in the surface and groundwater were studied. Hydrochemical data for surface water (4 samples) and groundwater (28 samples) were collected in a small watershed in the Poopó catchment at the highland of the Bolivian Andes (Altiplano). All of them show high electrical conductivity values and moderately oxidizing conditions. The surface water contains high concentration of sulfate and the trace elements As, Zn and Pb in the zone affected by acid mine drainage. There is a large variability of the concentration of As and of the trace elements in the groundwater in the five different regions within the Poopó catchment. The metal concentrations sensitive to changes of redox state and results of speciation modeling suggest that As (V) is a predominant aqueous species, which conforms to the prevailing oxidizing conditions in the shallow groundwater environment. Two generalized trends for As distribution were identified in groundwater: (a) high concentrations are found in the arid zone (100–250 μg/L) in the southern (region III) and in the northwestern (region V) regions, and (b) low concentrations (<50 μg/L) are found in the remaining part of the basin (region I, II and IV). However, the spatial distribution within these regions needs to be investigated further. A conclusion from the present study is that there are multiple sources of As as well as other trace elements (such as Cd, Mn and Zn) in the Poopó Lake Basin. Among the sources and the processes which led to the mobility of As and other trace metals in the region are: (a) weathering of sulfide minerals, (b) oxidation of pyrite and/or arsenopyrite in mineralized areas and (c) desorption from hydrous ferric oxide (HFO) surfaces. In non-mining areas, volcanic ash is suggested to be a significant source of As.  相似文献   

2.
The groundwater along the eastern escarpment of the Dead Sea shows a variety of chemical compositions with EC values ranging between 500 and a few thousand μS/cm. In this article the different groundwaters were correlated to the aquifers from where they originate and the water–rock interactions were elaborated at. It was found that the start of intercalations of Permo-Triassic and Jurassic rocks in the area and the basaltic dykes and sills are the sources, which cause a drastic increase in the salinity of the water. These rocks contents of residual evaporites, contact metamorphism products, sills, dykes and secondary altered mineral assemblage of plagioclase-, pyroxenes- and Fe-, Mn- minerals cause also drastic changes in ionic ratios, saturation indices and groundwater types. Fresh groundwater flows entering the area become, gradually, after a few kilometres highly salinized and of earthalkali type with prevailing chloride and sulfate instead of being bicarbonate waters.  相似文献   

3.
In this work the major and trace elements pollution levels in groundwater of Tuticorin city of Tamil Nadu was investigated. This coastal city with numerous large and small scale industries has increasingly affected the water quality by dumping effluents. The mean major and trace elements levels in groundwater in descending order: Si > Sr > Zn > Fe > Rb > Se > Al > Mn > Cu > As > Cr > Ba > V > Ni > Pb > Mo > Co > Sb > Cd > Ag. The concentrations of As, Se, Pb, Ba, Al, Fe and V (0.084, 0.150, 0.057, 0.837, 0.357 and 0.052) in some of the groundwater samples exceed the standard value of world health organization (WHO, 2004). Interrelationship between the elements was done by correlation matrix and factor analysis which indicates the contribution from industrial and irrigation fields. Spatial interpolation of inverse distance method (IDW) maps of all the elements suggested that discharge of effluents from chemical factory (STERLITE, TAC, SPIC, HEAVY WATER PLANT, NILA SEA FOODS), municipal wastewater, fertilizers were added to the natural sources. Results of this research suggests that proper measures should be taken to protect the vital groundwater resources in the Tuticorin city.  相似文献   

4.
Naturally-occurring radionuclides (uranium, radium, and radon), major dissolved constituents, and trace elements were investigated in fresh groundwater in 117 wells in fractured crystalline rocks from the Piedmont region (North Carolina, USA). Chemical variations show a general transition between two water types: (1) slightly acidic (pH 5.0–6.0), oxic, low-total dissolved solids (TDS) waters, and (2) near neutral, oxic to anoxic, higher-TDS waters. The uranium, radium, and radon levels in groundwater associated with granite (Rolesville Granite) are systematically higher than other rock types (gneiss, metasedimentary, and metavolcanic rocks). Water chemistry plays a secondary role on radium and radon distributions as the 222Rn/226Ra activity ratio is correlated with redox-sensitive solutes such as dissolved oxygen and Mn concentrations, as well as overall dissolved solids content including major divalent cations and Ba. Since 224Ra/228Ra activity ratios in groundwater are close to 1, we suggest that mobilization of Ra and Rn is controlled by alpha recoil processes from parent nuclides on fracture surfaces, ruling out Ra sources from mineral dissolution or significant long-distance Ra transport. Alpha recoil is balanced by Ra adsorption that is influenced by redox conditions and/or ion concentrations, resulting in an approximately one order of magnitude decrease (~ 20,000 to ~ 2000) in the apparent Ra distribution coefficient between oxygen-saturated and anoxic conditions and also across the range of dissolved ion concentrations (up to ~ 7 mM). Thus, the U and Th content of rocks is the primary control on observed Ra and Rn activities in groundwater in fractured crystalline rocks, and in addition, linked dissolved solids concentrations and redox conditions impart a secondary control.  相似文献   

5.
Fluid and mud samples were collected from Wushanting (WST), Hsiaokunshui (HKS), Yenshuikeng (YSK), Kuantzeling (KZL), and Kunshuiping (KSP) mud volcanoes of southwestern Taiwan. Concentrations of major ions and trace elements in mud volcanic fluids were analyzed to find the possible linkage to elevated arsenic (As) concentrations in the Chianan plain groundwater. The elevated Na+, K+, and Cl− concentrations indicated possible marine origin of the fluids. The trace element concentrations in the mud volcanic fluids were generally low, but the As concentrations were up to 0.12 mg/L. High contents of As, Fe, and Mn were observed in the mud samples. Saturation index calculations indicated that both carbonate and oxide minerals acted as potential sinks for As in the mud volcanic fluids. Arsenic in the dewatering fluids and muds may be transported by the subsurface flow and surface streams as suspended solids and eventually deposited in the Chianan plain aquifers. Under reducing conditions, As may be released from the host minerals (such as Fe- and Mn-oxides/hydroxides), thereby causing widespread groundwater As pollution.  相似文献   

6.
The distribution of several minor and trace elements mainly in fresh (dominating TDS 160–400 mg/l) groundwater of Latvia have been investigated by the Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) technique. An evaluation of results of about 700 analyses leads to the conclusion that concentrations of these elements is influenced by: pH–Eh conditions, groundwater residence time and diffuse contamination, whereas the role of water-bearing sediments is of secondary importance. Most trace elements are characterised by low mobility under alkaline and reducing conditions; concentrations in confined aquifers are much smaller than the Maximum Permissible Values for drinking water. The strongest anomalies of REE, Al and P were found in shallow groundwater around the former agrochemical storehouses.  相似文献   

7.
The chemical speciation of potentially toxic elements (As, Cd, Cu, Pb, and Zn) in the contaminated soils and sulfides-rich tailings sediments of an abandoned tungsten mine in Korea was evaluated by conducting modified BCR sequential extraction tests. Kinetic and static batch leaching tests were also conducted to evaluate the potential release of As and other heavy metals by acidic rain water and the leaching behaviors of these heavy metals. The major sources of the elements were As-, Zn- and Pb-bearing sulfides, Pb carbonates (i.e., cerussite), and Pb sulfates (i.e., anglesite). The biggest pollutant fraction in these soil and tailing samples consists of metals bound to the oxidizable host phase, which can be released into the environment if conditions become oxidative, and/or to residual fractions. No significant difference in total element concentrations was observed between the tailings sediments and contaminated soils. For both sample types, almost no changes occurred in the mobility of As and the other heavy metals at 7 days, but the mobility increased afterwards until the end of the tests at 30 days, regardless of the initial pH. However, the mobility was approximately 5–10 times higher at initial pH 1.0 than at initial pHs of 3.0 and 5.0. The leached amounts of all the heavy metal contents were higher from tailings sediments than from contaminated soils at pH > 3.0, but were lower at pH < 3.0 except for As. Results of this study suggest that further dissolution of heavy metals from soil and tailing samples may occur during extended rainfall, resulting in a serious threat to surface and groundwater in the mine area.  相似文献   

8.
Sulfide minerals commonly occur in sediments and basement rocks in southern New Zealand, as authigenic precipitates from groundwater below the oxygenated surface zone. There are two principal potential sources for sulfur in the groundwater system: weathering of sulfide minerals in the metamorphic basement and rainwater-derived marine aerosols. We present data for these two key sulfur sources: metamorphic sulfide and associated hydrothermal Au-bearing veins within the Otago Schist (average δ34S = −1.8 ± 2.4‰), and an inland saline lake (S derived entirely from rainwater, δ34S = 21.4 ± 0.8‰). We use these two end member δ34S values to estimate the contributions of these sources of sulfur in authigenic groundwater sulfide minerals and in waters derived from oxidation of these sulfide minerals, across a range of environments. We show that authigenic groundwater pyrite along joints in the Otago schist is derived primarily from metamorphic basement sulfur. In contrast, authigenic groundwater pyrite cementing Miocene-Recent aquifers shows a substantial marine aerosol component, and represents a distinct hydrogeological system. We suggest that marine aerosols represent a significant flux to the terrestrial sulfur cycle that has been present through the groundwater system in Otago over the past 20 million years.  相似文献   

9.
The study area covers two geologically different regions which have intensively been carpeted by tea plants in the eastern Black Sea. The rocks exposed in the region contain considerable amount of trace metals due to Upper Cretaceous massive sulfide formations and tertiary epithermal mineralizations. Tea plants that grow in soils derived from such mineralized rocks contain different concentrations of Cu, Pb, Zn, Fe, Cd, P, Al, Na, K, and S. The content ratios of most of the analyzed elements except Al are higher in basaltic and sedimentary rocks. To describe the transfer of metals from soil to tea leaf, the Freundlich-type model (log c plant = ac soil + log b) is used. The metal concentrations in leaves of tea plant in the studied soils are ranked as Zn > Cu > Pb > Al > Cd > Fe. The capacity of the plant to affect the metal accumulation decreased as follows: Fe > Cd > Pb > Cu > Zn > Al. Negative correlations were found between pH and availability of Cu, Pb, Zn, Mn, and Al elements by the tea plant. Experimental applications indicated that tea plant leaves growing on soils with high metal contents show some signs of toxicity. In soils where, particularly, ammonium sulfate fertilizer is used, metal uptake by the tea plant was found to be significantly higher as a result of extremely acidic character of the soil.  相似文献   

10.
《Applied Geochemistry》2002,17(5):583-603
This study identifies and quantifies the water–rock interactions responsible for the composition of 25 spring waters, and derives the weathering rates of rock-forming minerals in a complex of petrologic units containing ultramafics, amphibolites, augengneisses and micaschists. Bulk chemical analyses were used to calculate the mineralogical composition of these rocks; the composition of the rock-forming minerals were determined by microprobe analyses. The soils developed on augengneisses and micaschists contain predominantly halloysite; on the other units mixtures of halloysite and smectites. The mineralogical and chemical data on rocks and soils are essential for writing the proper weathering reactions and for solving mole balances between the amounts of weathered primary minerals and secondary products formed (soils and solutes in groundwater). Ground waters emanating in springs were collected in 3 consecutive seasons, namely late Summer, Winter and Spring, and analyzed for major components. Using an algorithm based on mole and charge balance equations, the average concentrations of the solutes were linked with a combination of possible weathering reactions. To sort out the best match of weathering reactions and the concomitantly generated water composition, the results were checked against the limiting condition of similarity between the predicted and actual clay mineral abundance in the soils. Having selected the best-fit weathering reactions, the mineral weathering rates could also be calculated by combining the median discharge rates and recharge areas of the springs and normalizing the rates by the mineral abundance. For the one case—plagioclase—for which comparison with published results was possible, the results compare favorably with rates calculated by other groups. For the most abundant primary minerals the following order of decreasing weathering rates was found (in moles/(ha·a·%mineral)): forsterite (485) > clinozoisite (114) > chlorite (49) > plagioclase (45) > amphibole (28). In as far as this order differs from commonly used orders of weatherability, this has to be due to differences in the hydrologic regime within this area and between this and other case studies. As additional objective, the authors wanted to explain the effects of contributions by sources other than water-rock interactions. The latter processes are coupled with acquisition of carbonate alkalinity and dissolved silica. Contributions by sources other than water–rock interactions are manifest by the Cl−, SO2−4 and NO−3 concentrations. It was possible to approximate the contribution of atmospheric deposition. More importantly, knowledge of the application and composition of fertilizers enabled assessment of the effects of farming on the composition of ground waters emanating in the springs. It was also possible to estimate how selective uptake of nutrients and cations by vegetation as well as ion-exchange processes in the soil modified the spring water composition. Using this rather holistic approach, it is possible to satisfactorily explain how spring waters, in this petrologically and agriculturally diverse area, acquired their composition.  相似文献   

11.
In this paper we provide a geochemical investigation on 34 groundwater samples in the Mt. Vulture volcanic aquifer representing one of the most important groundwater resources of the southern Italy pumped for drinking and irrigation supply. The present study includes the first data on the abundance and mobility of minor and trace elements and the thermodynamic considerations on water–rock interaction processes in order to evaluate the conditions of alkali basalt weathering by waters enriched in magma-derived CO2. The results highlight the occurrence of two hydrofacies: bicarbonate alkaline-earth and alkaline waters deriving from low-temperature leaching of volcanic rocks of Mt. Vulture, and bicarbonate-sulfate-alkaline waters (high-salinity waters) related to prolonged water circulation in alkali and feldspathoids-rich pyroclastic layers interbedded with clay deposits. The Al-normalized relative mobility (RM) of metals in Vulture's aquifer varies over a wide range (10− 1 < RM < 104), confirming that the basalt weathering is not a congruent and isochemical process. Chemical equilibrium studies show that the bicarbonate alkaline-earth and alkaline waters, having a short interaction with silicate minerals, plot very close to the kaolinite–smectite stability boundary, whereas the high-salinity waters fall in the stability field of smectite and muscovite because of prolonged interaction with alkali and feldspathoids-rich pyroclastic layers. Overall, for the bicarbonate alkaline-earth and alkaline waters, the release of toxic metals in solutions is related to the spatial variation of host-rock geochemistry, the high-salinity waters, collected near urban areas, show values higher than legal limits for Ni and As, likely as a consequence of anthropogenic contribution.  相似文献   

12.
The Carboniferous–Early Permian rift-related volcanic successions, covering large areas in the Chinese Tianshan and its adjacent areas, make up an important phanerozoic large igneous province in the word, which can be further divided into two sub-provinces: Tianshan and Tarim. The Early Permian volcanic rocks have been considered to be the products of an intraplate volcanism by most researchers. However, there is still strong controversy about the nature and geological setting of the Carboniferous volcanic rocks. The regional angular unconformity of Lower Carboniferous upon basement or pre-Carboniferous rocks, the ages (360–351 Ma) of the youngest ophiolite and the peak of subduction metamorphism of high pressure-low temperature metamorphic belt and the occurrence of Ni-Cu-bearing mafic-ultramafic intrusion with age of ~352 Ma and A-type granite with age of ~358 Ma reveal that the final closure of the Paleo-Asian Ocean might take place in the Early Mississippian. Our studies reveal that although contamination by continental crust or lithosphere can impart subduction-like signature (e.g., low Nb, low Ta and low Ti) and lead to misidentification of contaminated Carboniferous basaltic lavas from the Chinese Tianshan and its neighboring areas as arc related, there are still some essential differences between the Carboniferous basaltic lavas and arc related ones; such as: uncontaminated Carboniferous basaltic lavas have higher Nb concentrations (9–22 ppm), Nb/La > 1, “hump-shaped” OIB-like trace element patterns and moderate positive ɛNd values that distinguish them from the arc related ones; whereas, the contaminated Carboniferous basaltic lavas are characterized by pronounced negative Nb, Ta and Ti anomalies, but, their concentrations of incompatible trace elements are conspicuously higher than those of subduction-zone basalts that also distinguishes them from the arc related ones. Our summation suggests that the Carboniferous volcanic successions did indeed erupt in an intracontinental rift setting and their generation is likely confined to mantle plume.  相似文献   

13.
This study presents the data on the hydrochemical characteristics and isotope chemistry of Liwa aquifer, which could be useful to clarify the hydrochemical facies and hydrogeological regime in the study area. Electric conductivity and total dissolved solid values show that the investigated water is slightly brackish, due to the effect of evaporation and the occurrences of evaporite rocks in the adjacent Sabkhas of Abu Dhabi. Major cations and anions arranged according to their decreasing concentrations are: Na+ > Ca+2 > K+ > Mg+2 and Cl− > HCO3 − > SO4−2, respectively. As sodium is the dominate cation and chloride is the prevailing anion, hydrochemically the groundwater of Liwa can be classified as Na–Cl rich, predominantly chloridic. Ion concentrations increase towards the northeast and presumably coincide with the lithological sources of ions. Factors affecting the hydrochemistry of the groundwater of the investigated area include the effect of weathering of soil and rocks, evaporation and agricultural activities. Stable isotopes of oxygen and hydrogen show that the shallow aquifers contain a single water type that originated in a distinct climatic regime. This water type deviates from the local meteoric water line, as well as from the Eastern Mediterranean Meteoric Water Line, suggesting potential evaporation of recharged water prior to infiltration. The waters are poor in tritium, and thus can be considered generally as indication for recharge prior to 1952. The degradation of groundwater quality can be attributed to evaporation and agricultural practices in most cases.  相似文献   

14.
The solubility controls on vanadium (V) in groundwater were studied due to concerns over possible harmful health effects of ingesting V in drinking water. Vanadium concentrations in the northeastern San Joaquin Valley ranged from <3 μg/L to 70 μg/L with a median of 21 μg/L. Concentrations of V were highest in samples collected from oxic groundwater (49% > 25 μg/L) and lowest in samples collected from anoxic groundwater (70% < 0.8 μg/L). In oxic groundwater, speciation modeling (SM) using PHREEQC predicted that V exists primarily as the oxyanion H2VO4−. Adsorption/desorption reactions with mineral surfaces and associated oxide coatings were indicated as the primary solubility control of V5+ oxyanions in groundwater. Environmental data showed that V concentrations in oxic groundwater generally increased with increasing groundwater pH. However, data from adsorption isotherm experiments indicated that small variations in pH (7.4–8.2) were not likely as an important a factor as the inherent adsorption capacity of oxide assemblages coating the surface of mineral grains. In suboxic groundwater, accurate SM modeling was difficult since Eh measurements of source water were not measured in this study. Vanadium concentrations in suboxic groundwater decreased with increasing pH indicating that V may exist as an oxycationic species [e.g. V(OH)3+]. Vanadium may complex with dissolved inorganic and organic ligands under suboxic conditions, which could alter the adsorption behavior of V in groundwater. Speciation modeling did not predict the existence of V-inorganic ligand complexes and organic ligands were not collected as part of this study. More work is needed to determine processes governing V solubility under suboxic groundwater conditions. Under anoxic groundwater conditions, SM predicts that aqueous V exists as the uncharged V(OH)3 molecule. However, exceedingly low V concentrations show that V is sparingly soluble in anoxic conditions. Results indicated that V may be precipitating as V3+- or mixed V3+/Fe3+-oxides in anoxic groundwater, which is consistent with results of a previous study. The fact that V appears insoluble in anoxic (Fe reducing) redox conditions indicates that the behavior of V is different than arsenic (As) in aquifer systems where the reductive dissolution of Fe-oxides with As adsorbed to the surface is a well-documented mechanism for increasing As concentrations in groundwater. This hypothesis is supported by the relation of V to As concentrations in oxic versus anoxic redox conditions.Sequential extraction procedures (SEP) applied to aquifer material showed that the greatest amount of V was recovered by the nitric acid (HNO3) extract (37–71%), followed by the oxalate-ascorbic acid extract (19–60%) and the oxalate extract (3–14%). These results indicate that V was not associated with the solid phase as an easily exchangeable fraction. Although the total amount of V recovered was greatest for the HNO3 extract that targets V adsorbed to sorption sites of crystalline Al, Fe and Mn oxides, the greatest V saturation of sorption sites appeared to occur on the amorphous and poorly crystalline oxide solid phases targeted by the oxalate and oxalate-ascorbic acid extracts respectively. Adsorption isotherm experiments showed no correlation between V sorption and any of the fractions identified by the SEP. This lack of correlation indicates the application of an SEP alone is not adequate to estimate the sorption characteristics of V in an aquifer system.  相似文献   

15.
Uranium in spinel peridotite inclusions in basalts from Sardinia   总被引：2，自引：0，他引：2  
The uranium distribution in spinel peridotite inclusions and their host basalt from Sardinia, Italy, was determined by fission-track mapping. Whole-rock U concentrations range from 14 to 55 ppb. Although the partitioning of U among major silicate phases of the inclusions — olivine, orthopyroxene and clinopyroxene — remains roughly constant, the U content in the minerals is highly variable, e.g. ranging from 27 ppb to 177 ppb in clinopyroxene. The U variation in the minerals shows no apparent correlation with their major element chemistry. Liquid which equilibrated with the assemblages of inclusions with high U content, had U concentrations higher than those found in basaltic rocks. It is suggested that the inclusions were contaminated with a phase strongly enriched in U and subsequently recrystallized. The available data show that spinel peridotite inclusions of basaltic rocks frequently have complex multistage evolution and thus cannot provide a representative picture of the upper mantle radioactivity.  相似文献   

16.
A logistic regression model for the probability of arsenic exceeding the drinking water guidelines (10 μg/L) in bedrock groundwater was developed for a selected county in Korea, where arsenic occurrence and release reactions have been investigated. Arsenic was enriched naturally by the oxidation of sulfide minerals in metasedimentary rocks and mineralized zones, and due to high mobility in alkaline pH conditions, concentrations were high in groundwater of the county. When considering these reactions of arsenic release and water quality characteristics, several geological and geochemical factors were selected as influencing variables in the model. In the final logistic regression model, geological units of limestone and metasedimentary rocks, the concentrations of nitrate and sulfate, and distances to closed mines and adjacent granite were retained as statistically significant variables. Predicted areas of high probability agreed well with known spatial contamination patterns in the county. The model was also applied to an adjacent county, where the groundwater has not previously been tested for the presence of arsenic, and a probability map for arsenic contamination was then produced. Through the analysis of arsenic concentrations at the wells of high probability, it was determined that the applied model accurately indicated the arsenic contamination of groundwater. The logistic regression approach of this study can be applied to predict arsenic contamination in areas of similar geological and geochemical conditions to the county used in this model.  相似文献   

17.
It is hypothesized that hydrochemical parameters can be employed to deduce the basaltic trap thickness and that there exist diverse hydrochemical processes within the existing host rocks along the Deccan Volcanic Province (DVP) margin. Chemical imprints of aquifers, in various flows of flood basalt and fissured zones of granites, had been appraised using major ion chemistry of groundwater in a test site of 623 km2 at the southern margin of the DVP in India. The wide ranging hydrochemical processes, obtained from empirical data, describe the predominance of carbonate, dolomite, calcite and anorthite weathering in basalts, and alkali feldspar (albite and orthoclase) in granites. Results showed that the elevated concentrations of alkaline earth elements in basaltic aquifers and alkali rich elements in granitic aquifers were useful in tracing the sources of host rock for dissolved mineral reactants. Further, a digital elevation model using Shuttle Radar Topography Mission (90 m) elevation satellite data aided in deciphering trap thickness, vertical transition zone of trap and granitic basement comprising the well depths and hydrochemistry. The mapping of trap thickness is useful to explore the groundwater resources at the vertical transition zone between the basaltic trap and granitic base. The estimated thickness of the basaltic trap is varied from 4 to 98 m at the DVP southern margin, which is further verified with the help of exploratory well lithologs matched closely.  相似文献   

18.
Distribution of fluoride in groundwater of Maku area, northwest of Iran   总被引：3，自引：0，他引：3  
High fluoride groundwater occurs in Maku area, in the north of West Azarbaijan province, northwest of Iran. Groundwater is the main source of drinking water for the area residents. Groundwater samples were collected from 72 selected points including 40 basaltic and 32 nonbasaltic springs and wells, in two stages, during June and August 2006. The areas with high fluoride concentrations have been identified, and the possible causes for its variation have been investigated. Regional hydrogeochemical investigation indicates that water-rock interaction is probably the main reason for the high concentration of ions in groundwater. The concentration of F− in groundwater is positively correlated with that of HCO3 − and Na+, indicating that groundwater with high HCO3 − and Na+ concentrations help to dissolve some fluoride-rich minerals. All of the water samples, collected from the basaltic areas do not meet the water quality standards for fluoride concentration and some other parameters. Hence, it is not suitable for consumption without any prior treatment. Inhabitants of the area that obtain their drinking water supplies from basaltic springs and wells are suffering from dental fluorosis. The population of the study area is at a high risk due to excessive fluoride intake especially when they are unaware of the amount of fluoride being ingested due to lack of awareness.  相似文献   

19.
This paper presents the results of experimental study of fluorine leaching from rocks of various basicity by distilled water and multicomponent organic acid solution, in which the frequency distribution of dissociation constants of carboxyl groups correspond to that of natural soil solutions. It is shown that organic acids significantly enhance the intensity of fluorine leaching from rocks as compared to distilled water. A positive correlation was established between fluorine and magnesium extracted from different rocks by organic acids (r = 0.92). The correlation between fluorine and other main petrogenic elements is absent. Intensity of fluorine mobilization from rocks under the action of organic acids increases with the growth of basicity of the rocks with decreasing their chemical stability in the following sequence: meimechite > basaltic andesite > albitized rhyodacite > alkaline agpaitic granite.  相似文献   

20.
Elevated As concentrations in groundwater in the eastern United States have been recognized predominantly in the accretionary geologic terranes of northern New England. A retrospective examination of more than 18,000 existing groundwater samples from the Pennsylvania Department of Environmental Protection (PA DEP) Drinking Water and Sampling Information System database indicates that elevated groundwater As concentrations occur throughout the northern half of the Piedmont Province of Pennsylvania. Chemical analyses of 53 samples collected in 2005 from drinking water wells in this area all had detectable As, and 23% of these samples contained elevated (>133 nmol/L or >10 μg/L) concentrations of As. Elevated concentrations of As in the groundwater samples were most common in the Mesozoic sedimentary strata composed of sandstone and red mudstone with interbedded gray shale, and gray to black siltstone and shale. Arsenic was typically not elevated in groundwater of diabase intrusions of the Newark Basin or in crystalline and calcareous aquifers to the north of the Newark Basin. Geochemical parameters such as pH and oxidation–reduction potential can indicate mobility mechanisms of As in some regions. In this area, measured groundwater conditions were predominantly oxidizing (Eh > +50 mV), and more than 85% of samples contained arsenate as the dominant As species. Variations in pH were strongly correlated to the As concentration, with highest As concentrations observed at pH values greater than 6.4. The original source of As is most likely the black and gray shales that contain some arsenian pyrite with groundwater concentrations likely to be controlled by adsorption/desorption reactions with Fe oxides in the red mudstone aquifer materials.  相似文献   

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