首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
Groundwaters and surface water in the Shihongtan sandstone-hosted U ore district, Xinjiang, NW China, were sampled and analyzed for their major-, and trace element concentrations and oxygen, hydrogen, boron and strontium isotope compositions in order to assess the possible origins of the waters and water–rock interactions that occurred in the deep aquifer system. The waters in the study district have been grouped into three hydrochemical facies: Facies 1, potable spring-water, is a pH neutral (7.0), Na–Ca–HCO3 type water with low total dissolved solids (TDS; 0.2 g/l, fresh) and has δ18O of − 8.3‰, δD of − 48.2‰,δ11B of 1.5‰, and 87Sr/86Sr of 0.70627. Facies 2 groundwaters are mildly acidic to mildly alkaline (pH of 6.5–8.0, mean 7.3), Na–Ca–Mg–Cl–SO4 type waters with moderate TDS (8.2 g/l–17.2 g/l, mean 9.3 g/l, brackish) and haveδ18O values in the − 5.8‰ to − 9.3‰ range (mean − 8.1‰), δD values in the − 20.8‰ to − 85.5‰ range (mean − 47.0‰),δ11B values in the + 9.5‰ to + 39.1‰ range (mean + 17.1‰), and 87Sr/86Sr values in the 0.70595 to 0.70975 range (mean 0.70826). Facies 3, Aiting Lake water, is a mildly alkaline (pH = 7.4), Na–Ca–Mg–Cl–SO4 type water with the highest TDS (249.1 g/l, brine) and has δ18O of − 2.8‰, δD of − 45.8‰,δ11B of 21.2‰, and 87Sr/86Sr of 0.70840. The waters from the study district show a systematic increase in major, trace element and TDS concentrations and δ11B values along the pathway of groundwater migration which can only be interpreted in terms of water–rock interaction at depth and strong surface evaporation. The hydrochemical and isotopic data presented here confirm that the groundwaters in the Shihongtan ore district are the combined result of migration, water–rock interaction and mixing of meteoric water with connate waters contained in sediments.  相似文献   

2.
Data are presented on rare-earth elements (REE) in prefiltered (<450 nm) near-surface and deeper groundwaters and in corresponding particulate matter (>450 nm) from the Osamu Utsumi uranium mine and the Morro do Ferro thorium-REE-deposit. Groundwaters from both sites typically contain between 1–50 μg/l of total REE, but can reach values of up to 160 μg/l in the deepest borehole F4 (U-Mine: 150–415 m). Even higher REE concentrations of up to 29 mg/l were measured in acidic, sulfate-rich near-surface waters of the same site. The chondrite-normalized REE patterns in deeper, more reducing groundwaters and in their corresponding suspended particle fractions are similar to those observed in the bedrock (phonolites), indicating that bedrock leaching and secondary mineral sorption occurred without significant fractionation between these elements, in accordance with the only small variations in the stability constants of the expected REE-sulfate complexes in these waters. Groundwaters from the unsaturated zone of both sites show a very characteristic cerium depletion (less pronounced than that observed in the corresponding suspended particulate fractions), which is most probably related to the oxidation of Ce (III) under the prevailing Eh-conditions of these waters (600 to 800 mV), and to sorption/precipitation reactions of the much less soluble Ce(IV) species. Coarse particulate matter (>450 nm), composed mainly of amorphous ferric hydrous oxides, has a strong capacity for sorption of REE. This is shown by its very high REE concentrations, in some boreholes > 8,000 μg/g (total REE), and by the calculated association ratios Ra (ml/g), which are in the order of 105 to 106. The implications of these findings for the migration behavior of REE in both environments are discussed.  相似文献   

3.
In the Pine Creek Geosyncline, fast moving, annually recharged, low-salinity ground waters dissolve uranium- and magnesium-enriched gangue minerals from mineralized aquifer rocks. The level of dissolved uranium depends on prevailing pH, Eh, salinity and degree of adsorption, which limits its effectiveness as an exploration indicator. Near each known deposit, leaching of magnesium-enriched gangue minerals produces ground waters with very similar major-element concentration plots, the shape of which constitutes a mineralized aquifer “signature”. Gangue minerals also supply high levels of Mg2+ (expressed as NMg = [Mg2+]/[Ca2+ + Mg2+ + Na+ + K+] in milliequivalents per litre) to contained ground waters, NMg > 0.8 being common in ground waters from mineralized aquifers at each Pine Creek Geosyncline deposit. Data from Ranger One No. 3 ore body illustrates how progressive mixing of waters from mineralized and unmineralized aquifers causes graded reductions in NMg, which, when plotted onto a ground plan, delineate a hydrogeochemical aureole.High NMg (> 0.8) coincides with high uranium concentration (> 20 μg/l of U) in ground waters near Nabarlek and Ranger. Because pH-Eh conditions in aquifers at Jabiluka depress uranium solution, < 10 μg/l of U is present, although NMg values are generally > 0.8. To date NMg has always been < 0.8 in nonmineralized aquifer waters, whereas uranium may be > 50 μg/l in ground waters from felsic igneous aquifers, which can be identified as uneconomic by low (< 0.4) NMg, and by a fixed relationship between uranium and co-leached species such as F- and soluble salts.Measurements of pH, Eh, salinity, Fe(II), Ca, Mg, Na, K, Cl, SO4, total carbonate, phosphate, F-, Cu, Pb, Zn and U in waters from 48 percussion holes in and near the Koongarra ore bodies have been related to mineralogy recorded in drill logs. The composition of waters from 20 holes near and along strike from known mineralization, fitted the mineralized aquifer “signature”, had NMg > 0.8 and uranium up to 4100 μ/l. These data confirm the use in this region of NMg as a hydrogeochemical indicator of uranium mineralization; they also indicate additional zones of possible mineralization.  相似文献   

4.
A case study of three springs in Switzerland is used to demonstrate the value of geochemical time-series data as a powerful tool to study the dynamics of groundwater systems. Values of repeatedly measured parameters revealed intermixings of two water types: (a) a 29°C water, circulating to a depth of 1100 m and containing approximately 700 mg/l Ca, 2000 mg/l SO4, 700 mg/l HCO3, 20 mg/l of Na and Cl, 6 mg/l Fe, at least 47 mg/l SiO2, and with an isotopic composition of δD = − 73.0‰ and δ18 O = −10.9‰, and (b) a 12°C or colder water, shallow, and of a post-1953 age, containing 420 mg/l TDI or less, very low in Na and Cl (4 mg/l or less), isotopic values of δD = −71.0‰ and δ18 O = −10.5‰ and tritium as in recent (post-bomb) precipitation.  相似文献   

5.
A carbonate-hosted stratabound siliceous crust type (SCT) mineralization (base metal sulphides, barite, fluorite) occurs over large areas of Carnic Alps and Karawanken in the Eastern Alps. It concerns a pervasively silicified lithological unit, up to some tens of metres thick, which caps the unconformity landscapes developed on epicontinental Devonian–Dinantian carbonates. The SCT mineralization is directly overlaid by different transgressive siliciclastic sediments, which range from Lower Carboniferous to Lower Permian. The presence of fragments of the SCT mineralization in the transgressive siliciclastic sediment bounds its whole lithological evolution within a short stratigraphic interval of Lower Carboniferous age. Selected features of the regional and lithostratigraphic setting are discussed. The chemical characterisation is based on the statistical evaluation of compositional data of 581 selected samples. Three significant groups of elements have been distinguished: (1) the hydrological and metasomatically active elements (Si, Ba, F), which show a strong negative correlation amongst themselves and characterise the silica-saturated aqueous solutions; (2) the terrigenous elements (Al2O3, K2O, Fetot, TiO2, B, Be, Ce, La, Nb, V, Y, Zr), which suggest a continental margin environment for silica deposition; (3) the sulphide metals (Cu, Pb, Zn, Ni, Sb, As, Hg, Cd), which define the metalliferous signature of the SCT mineralization.Some consistent, but still debatable genetic aspects of the SCT mineralization are as follow: (1) silica may be supplied by illitization of clay-rich basinal sediments during their diagenesis. δ18O of microcrystalline quartz ranges from +18.5‰ and +24.6‰ and is very similar to δ18O of authigenic quartz deriving from diagenetic processes of illitization of clay-rich basinal sequences. (2) The diagenetic evolution of these sediments may trigger off the movement of silica-rich marine pore waters. δ34S of barite ranges from +15.5‰ to +19.3‰ with an average of +17.7‰ and are in good agreement with δ34S of sulphate in ocean waters of Upper Devonian–Lower Carboniferous age. (3) A convective hydrological system, connected with sinsedimentary transtensive tectonics, active in the Carnic Alps since the Frasnian, may be the transport mechanism of aqueous solutions. (4) A weak drop in pH in the dominant carbonate environment represents the conditions for silica precipitation.SCT mineralization, showing persistent, independent and distinct characters, occurs over large areas also in other sites of the Alpine belt and outside Italy and Austria. Therefore, it points to important markers for some sedimentary sequences as well as to a worldwide significant cyclic metallogenic event. It represents a new ore deposit-type within the carbonate-hosted mineralization.  相似文献   

6.
Sulfur and O isotope analyses of dissolved SO4 were used to constrain a hydrogeological model for the area overlying the Gorleben–Rambow Salt Structure, Northern Germany. Samples were collected from 80 wells screened at different depth-intervals. The study area consists of a set of two vertically stacked aquifer systems. Generally, the isotope data show a good spatial correlation, outlining well-defined groundwater zones containing SO4 of characteristic isotopic composition. Highly saline waters from deeper parts of the lower aquifer system are characterized by rather constant SO4 isotopic compositions, which are typical of Permian Zechstein evaporites (δ34S=9.6–11.9‰; δ18O=9.5–12.1‰). Above this is a transition zone containing ground waters of intermediate salinity and slightly higher isotopic values (average δ34S=16.6‰; δ18O=15.3‰). The confined groundwater horizon on the top of the lower aquifer system below the low permeable Hamburg Clays is low in total dissolved solids and is characterized by an extreme 34S enrichment (average δ34S=39.1‰; δ18O=18.4‰), suggesting that bacterially mediated SO4 reduction is a dominant geochemical process in this zone. Two areas of distinct isotopic composition can be identified in the shallow ground water horizons of the upper hydrogeological system. Sulfate in groundwaters adjacent to the river Elbe and Löcknitz has a typical meteoric isotopic signature (δ34S=5.2‰; δ18O=8.2‰), whereas the central part of the area is characterized by more elevated isotopic ratios (δ34S=12.7‰; δ18O=15.6‰). The two major SO4 pools in the area are represented by Permian seawater SO4 and a SO4 of meteoric origin that has been mixed with SO4 resulting from the oxidation of pyrite. It is suggested that the S-isotope compositions observed reflect the nature of the SO4 source that have been modified to various extent by bacterial SO4 reduction. Groundwaters with transitional salinity have resulted from mixing between brines and low-mineralized waters affected by bacterial SO4 reduction.  相似文献   

7.
This paper reviews the geochemical, isotopic (2H, 18O, 13C, 3H and 14C) and numerical modelling approaches to evaluate possible geological sources of the high pH (11.5)/Na–Cl/Ca–OH mineral waters from the Cabeço de Vide region (Central-Portugal). Water–rock interaction studies have greatly contributed to a conceptual hydrogeological circulation model of the Cabeço de Vide mineral waters, which was corroborated by numerical modelling approaches. The local shallow groundwaters belong to the Mg–HCO3 type, and are derived by interaction with the local serpentinized rocks. At depth, these type waters evolve into the high pH/Na–Cl/Ca–OH mineral waters of Cabeço de Vide spas, issuing from the intrusive contact between mafic/ultramafic rocks and an older carbonate sequence. The Cabeço de Vide mineral waters are supersaturated with respect to serpentine indicating that they may cause serpentinization. Magnesium silicate phases (brucite and serpentine) seem to control Mg concentrations in Cabeço de Vide mineral waters. Similar δ2H and δ18O suggest a common meteoric origin and that the Mg–HCO3 type waters have evolved towards Cabeço de Vide mineral waters. The reaction path simulations show that the progressive evolution of the Ca–HCO3 to Mg–HCO3 waters can be attributed to the interaction of meteoric waters with serpentinites. The sequential dissolution at CO2 (g) closed system conditions leads to the precipitation of calcite, magnesite, amorphous silica, chrysotile and brucite, indicating that the waters would be responsible for the serpentinization of fresh ultramafic rocks (dunites) present at depth. The apparent age of Cabeço de Vide mineral waters was determined as 2790 ± 40 a BP, on the basis of 14C and 13C values, which is in agreement with the 3H concentrations being below the detection limit.  相似文献   

8.
This work reports new hydrochemical data on the two types of cold high p CO2 groundwaters from the Mukhen deposit (Khabarovsk district). The first type is classed with HCO3-Ca-Mg waters with a relatively low TDS (up to 1.7 g/l) and high concentrations of Fe2+, Mn2+, Ba2+, and SiO2. The second type is of HCO3-Na composition with high TDS (up to 14 g/l) and elevated Li+, B, Sr2+, Br?, and I?. New oxygen (δ18O) and hydrogen (δD) isotopic data on the waters and carbon (δ13C) isotopic data on the gas phase, together with a detailed geological and hydrogeological analysis of the study area, allowed us to decipher the origin of both the mineral waters. Based on the tritium content (3H) in the ground and surface waters of the area, the duration of the mineral water circulation was estimated. It was established that the both types of groundwaters were formed during interaction of meteoric water with bedrock under active influence of CO2, however HCO3-Na groundwaters have longer residence time than HCO3-Ca-Mg groundwaters.  相似文献   

9.
The possible contamination of a groundwater system with industrial wastewater originating from a paper mill factory has been investigated in Piteå, N. Sweden. Six samples were collected from the wastewater in the waste dump and twelve samples from the adjacent groundwater were analyzed for chemistry and sulfur isotopes. The industrial wastewater is a saline water consisting mainly of Na–HCO3–SO4, having a high pH and showing δ34S values between 7‰ and 9‰ affected by bacterial sulfate reduction. The groundwaters are relatively dilute, dominated by Na+, Ca2+ and HCO3−, but with varying concentrations as exemplified by sulfate with concentrations varying between 3 and 69 mg L− 1 while the δ34S values range from − 0.5‰ to 14.3‰. The data suggest that the main S sources in the waters are the bedrock sulfides and/or atmospheric deposition, which, sometimes, are overlapped by bacterial sulfate reduction. Contamination from the waste dump does not occur.  相似文献   

10.
Detailed hydrogeochemical and isotopic data of groundwaters from the Hammamet–Nabeul unconfined aquifer are used to provide a better understanding of the natural and anthropogenic processes that control the groundwater mineralization as well as the sources of different groundwater bodies. It has been demonstrated that groundwaters, which show Na–Cl and Ca–SO4–Cl water facies, are mainly influenced by the dissolution of evaporates, the dedolomitization and the cation-exchange process; and supplementary by anthropogenic process in relation with return flow of irrigation waters. The isotopic signatures permit to classify the studied groundwaters into two different groups. Non-evaporated groundwaters that are characterized by depleted δ 18O and δ 2H contents highlighting the importance of modern recharge at higher altitude. Evaporated groundwaters with enriched contents reflecting the significance infiltration of return flow irrigation waters. Tritium data in the studied groundwaters lend support to the existence of pre-1950 and post-1960 recharge. Carbon-14 activities in shallow wells that provide evidence to the large contamination by organic 14C corroborate the recent origin of the groundwaters in the study area.  相似文献   

11.
Groundwaters in the confined aquifers of the Chianan and Ilan coastal plains of Taiwan are rich in dissolved methane (CH4). Serious endemic “blackfoot disease”, which occurred in the Chianan plain, especially during AD1950-1970, has been demonstrated to have arisen from drinking highly reducing groundwater with abnormal arsenic and humic substance levels. In order to explore the origin of CH4 and its hydrological implications, stable carbon isotope ratios (δ13C) and radiocarbon (14C) ages of exsolved CH4, dissolved inorganic carbon (DIC), and sedimentary biogenic sediments from a total of 34 newly completed water wells at 16 sites were determined. The main results obtained are as follows: (1) The δ13CCH4 (−65‰ to −75‰) values indicate that, except for one thermogenic sample (δ13CCH4=38.2‰) from the Ilan plain, all CH4 samples analyzed were produced via microbially mediated CO2 reduction. Many δ13CDIC values are considerably greater than −10‰ and even up to 10‰ due to Rayleigh enrichment during CO2 reduction. (2) Almost all the 14C ages of CH4 samples from the shallow aquifer (I) (<60 m depth) are greater than the 14C ages of coexisting DIC and sediments, suggesting the presence of CH4 from underlying aquifers. (3) The 14C ages of coexisting CH4, DIC and sediments from aquifer (II) of the Chianan plain are essentially equal, reflecting in-situ generation of CH4 and DIC from decomposition of sedimentary organic matter and sluggishness of the groundwater flow. On the other hand, both CH4 and DIC from each individual well of the relatively deep aquifers (III) and (IV) in the Chianan plain are remarkably younger than the deposition of their coexisting sediments, indicating that current groundwaters entered these two aquifers much later than the deposition of aquifer sediments. (4) Each CH4 sample collected from the Ilan plain is older than coexisting DIC, which in turn is distinctly older than the deposition of respective aquifer sediments, demonstrating the presence of much older CO2 and CH4 from underlying strata.  相似文献   

12.
High concentrations of U and226Ra, and elevated234U/238U activity ratios have been measured in groundwater samples collected from water supply wells and exploratory boreholes in the area surrounding the Underground Research Laboratory (URL) of Atomic Energy of Canada Limited, in southeastern Manitoba. All groundwaters come from the Lac du Bonnet granite batholith or sediments overlying the batholith.Uranium concentrations attain almost 1 mg/l in some shallow, low-salinity groundwaters, whereas226Ra tends to be high (up to 38 Bq/l) in deeper, saline waters. The U concentrations are some of the highest observed in global groundwaters, yet no significant ore body or mineralization is known in the area. Analyses of unaltered rock samples of the Lac du Bonnet granite show slight U enrichment over average Canadian Shield granites (6.5 μg/g vs 4 μg/g), and altered wall rock in fracture zones is enriched in U by up to an order of magnitude compared to adjacent bedrock. Low234U/238U activity ratios in this altered rock indicate active and recent leaching of U by groundwater.The key control on U concentration appears to be redox potential. Concentrations of U in rock, residence time and groundwater composition are of lesser importance. Geochemical modelling of the shallower, oxidized waters indicates that U speciation consists mainly of anionic carbonate complexes of the uranyl ion. This is supported by the remarkable efficiency of an anionic filter developed to remove high levels of U from drinking water in the area.In more reducing groundwaters, U concentrations are similar to those determined in recent experimental work on uraninite solubility in the pH range 7–8.5. Colloidal U is <10% of total U and organic complexation is unlikely to be significant because of low dissolved organic concentrations. The results emphasize the significance of redox potential in controlling U mobility in both oxidizing and reducing environments and indicate the usefulness of U concentration in estimating groundwater Eh.  相似文献   

13.
The potential for using groundwater helium surveys in exploration has been evaluated by conducting local and regional surveys in several mineralized and background areas in Australia. Dissolved helium contents decrease markedly upwards, particularly in the top 10–15m, due to degassing in attaining dynamic equilibrium with the atmosphere. Gradients of depth profiles are not uniform but because total concentration variations to 50m or more are commonly less than 10, whereas regional variations are 103–105, samples from the greatest constant depth possible below water-table are adequate for survey purposes. Helium concentrations in excess of the atmosphere equilibrium value of 0.044 μl He/l H2O were found to be associated with uranium mineralization at Honeymoon (6.9–44.4 μl/l), Manyingee (0.08–1.68 μl/l), Bennett Well (9.9–29.5 μ/l) and the Stuart Shelf—Roxby Downs (910–2495 μl/l), with a carbonatite at Mt. Weld (0.18–13.6 μl/l), and with kimberlites at Wandagee (0.2–3.25 μl/l). No anomaly was associated with the shallow calcrete uranium deposit at Yeelirrie. However, equivalent or higher concentrations were found in groundwaters from unmineralized areas around these deposits, e.g. up to 85 μl/l at Manyingee—Bennett Well, to 215 μl/l at Yeelirrie and to 1525 μl/l, Stuart Shelf—Mt. Gunson. Similarly, helium in waters from stock wells near Mt. Weld appears to indicate the presence of the carbonatite but in a survey of a geologically similar area near Malcolm, equivalent anomalies were not related to carbonatite.Although the uranium (and thorium) mineralization is a significant source, high helium concentrations can arise by accumulation in groundwaters with long residence times and by leakage from deep sources, particularly granitoid basement. The concentration reached is also a function of the porosity and configuration of the aquifer and the permeability of the aquiclude to helium. These factors are more important in determining dissolved helium concentrations than the uranium and thorium contents of the rocks. However, the effects are not readily quantifiable, particularly in exploration areas where geology and hydrology are relatively unknown, hence helium groundwater data can be difficult if not impossible to interpret.  相似文献   

14.
New major, trace and isotopic geochemical results from a regional study of springs discharging from the major carbonate rock aquifer in the Interlake Region of Manitoba, Canada, are used to understand water–rock reactions, timing of recharge/discharge, tufa formation processes, and as baseline data. Spring waters are fresh with total dissolved solids (TDS) concentrations ranging from 150 to 880 mg/L. Waters discharging in the northern part of the study area have lower TDS, are dominantly Ca–Mg–HCO3 waters with low SO4 concentrations (<< 50 mg/L), and appear to have interacted primarily with Silurian carbonate lithologies. In contrast, waters in the southeastern part of the study area have higher TDS and have elevated SO4 concentrations (up to 210 mg/L). Spring waters have elevated Mg/Camolar (1.23 ± 0.23), typically greater than congruent dissolution of dolomite. Ca and Mg concentrations and Mg/Camolar indicate that groundwater residence times were sufficient to allow equilibration with bedrock dolomite lithologies; elevated tritium in northern waters indicates a significant recharge component in the 1960's and 1970's. Tufa precipitates that have formed from many of the spring waters are low-Mg calcite (MgO = 1.70 to 5.80 wt.%). Sr concentrations are variable (57 to 657 ppm) and tufa Sr/Camolar ratios appear to be entirely controlled by spring water Sr/Camolar. Empirically determined Sr distribution coefficients (DSr = 0.389 ± 0.083) indicate rapid crystallization following CO2 degassing, consistent with heavier δ13CVPDB compared to spring waters. Sulfate concentrations are generally too low for calcitization (dedolomitization) reactions driven by anhydrite dissolution to be the dominant control on the elevated groundwater Mg/Camolar, implying either extensive sulfate reduction along the flow paths (however, δ13CDIC suggests the elevated SO4 is more consistent with Fe-sulfide oxidation), or that other processes are involved. Major ion ratios suggest that the waters in the southern part of the study area are more consistent with interaction with siliciclastic rocks than with anhydrite dissolution. We suggest that calcitization (dedolomitization) reactions driven by anhydrite dissolution may not dominate all carbonate aquifers and that mixing of waters in karst conduits combined with ion exchange reactions are important controls on water chemistry in these systems.  相似文献   

15.
Stable isotope ratios of oxygen and carbon were determined for CO2 in soil gas in the vicinity of the massive sulfide deposit at Crandon, Wisconsin with the objective of determining the source of anomalously high CO2 concentrations detected previously by McCarthy et al. (1986). Values of δ13C in soil gas CO2 from depths between 0.5 and 1.0 m were found to range from −12.68‰ to −20.03‰ (PDB). Organic carbon from the uppermost meter of soil has δ13C between −24.1 and −25.8‰ (PDB), indicating derivation from plant species with the C3 (Calvin) type of photosynthetic pathway. Microbial decomposition of the organic carbon and root respiration from C3 and C4 (Hatch-Slack) plants, together with atmospheric CO2 are the likely sources of carbon in soil gas CO2. Values of δ18O in soil-gas CO2 range from 32 to 38‰ (SMOW). These δ18O values are intermediate between that calculated for CO2 gas in isotopic equilibrium with local groundwaters and that for atmospheric CO2. The δ18O data indicate that atmospheric CO2 has been incorporated by mixing or diffusion. Any CO2 generated by microbial oxidation of organic matter has equilibrated its oxygen isotopes with the local groundwaters.The isotopic composition of soil-gas CO2 taken from directly above the massive sulfide deposit was not distinguishable from that of background samples taken 1 to 2 km away. No enrichment of the δ13C value of soil-gas CO2 was observed, contrary to what would be expected if the anomalous CO2 were derived from the dissolution of Proterozoic marine limestone country rock or of Paleozoic limestone clasts in glacial till. Therefore, it is inferred that root respiration and decay of C3 plant material were responsible for most CO2 generation both in the vicinity of the massive sulfide and in the “background” area, on the occasion of our sampling. Interpretation of our data is complicated by the effects of rainfall, which significantly reduced the magnitude of the CO2 anomaly. Therefore, we cannot rule out the possible mechanism of carbonate dissolution driven by pyrite oxidation, as proposed by Lovell et al. (1983) and McCarthy et al. (1986). Further work is needed on seasonal and daily variations of CO2 concentrations and stable isotope ratios in various hydrogeologic and ecologic settings so that more effective sampling strategies can be developed for mineral exploration using soil gases.  相似文献   

16.
Different types of free water have been analysed for their deuterium and chemical composition in order to evaluate their source, mixing phenomena, and the underground dynamics. All types of ground water (mineral, geothermal and wellhead water) display δD values (− 82.6‰ to − 72.6‰) similar to surface waters from the studied area (− 77.1‰ to − 73.6‰). The global salt content varies from 1102 to 8707 mg/l for the groundwater, and from 46 to 392 mg/l for the surface water. From the co-variation between the δD values and the chemical composition of the waters, as well as from the seasonal variation of these two parameters, it is evident that the free water from Tuşnad Băi are meteoric in origin. The mineralization of the mineral water took place by means of an intense underground circulation, probably in the fault system developed within the Neogene magmatites.  相似文献   

17.
Oil-field brines are the most favored ore-forming solutions for the sediment-hosted Mississippi Valley-type ore deposits. Detailed inorganic and organic chemical and isotope analyses of water and gas samples from six oil fields in central Mississippi, one of the very few areas with high metal brines, were conducted to study the inorganic and organic complexes responsible for the high concentrations of these metals. The samples were obtained from production zones consisting of sandstone and limestone that range in depth from 1900 to 4000 m (70–120°C) and in age from Late Cretaceous to Late Jurassic. Results show that the waters are dominantly bittern brines related to the Louann Salt. The brines have extremely high salinities that range from 160,000 to 320,000 mg/l total dissolved solids and are NaCaCl-type waters with very high concentrations of Ca (up to 48,000 mg/l) and other alkaline-earth metals, but with low concentrations of aliphatic acid anions. The concentrations of metals in many water samples are very high, reaching values of 70 mg/l for Pb, 245 mg/l for Zn, 465 mg/l for Fe and 210 mg/l for Mn. The samples with high metal contents have extremely low concentrations (<0.02 mg/l) of H2S. Samples obtained from the Smackover Formation (limestone) have low metal contents that are more typical of oil-field waters, but have very high concentrations (up to 85 mg/l) of H2S. Computations with the geochemical code SOLMINEQ.87 give the following results: (1) both Pb and Zn are present predominantly as aqueous chloride complexes (mainly as PbCl42− and ZnCl42−, respectively); (2) the concentrations of metals complexed with short-chained aliphatic acid anions and reduced S species are minor; (3) organic acid anions are important in controlling the concentrations of metals because they affect the pH and buffer capacity of the waters at subsurface conditions; and (4) galena and sphalerite solubilities control the concentrations of Pb and Zn in these waters.  相似文献   

18.
《Applied Geochemistry》2004,19(4):519-560
The hydrogeochemistry of the Lac du Bonnet granitic batholith has been determined for the region of the Whiteshell Research Area (WRA) in southeastern Manitoba, Canada. This work forms part of the geosciences studies performed for the Canadian Nuclear Fuel Waste Management Program over the period 1980–1995 by Atomic Energy of Canada Limited (AECL). Knowledge of the variation of groundwater chemistry and its causes is useful in assessing the performance and safety of a nuclear fuel waste vault located at depths of up to 1000 m in a crystalline rock formation of the Canadian Shield. Groundwaters and matrix pore fluids have been obtained by standard sampling methods from shallow piezometers in clay-rich overburden, from packer-isolated borehole zones intersecting fractures or fault zones in the bedrock, and from boreholes in unfractured rock in AECL's Underground Research Laboratory (URL). Eighty-six individual fracture groundwaters have been sampled and analysed from permeable zones in 53 boreholes drilled to depths of up to 1000 m in the Lac du Bonnet batholith. In addition, 28 groundwaters from piezometers in a large wetland area near the URL have been sampled and analysed to determine the influence of clay-rich overburden on the bedrock hydrogeochemistry. Analyses have been made for major and minor ions, pH, Eh, trace metals, and stable and radioactive isotopes, to characterise these groundwaters and relate them to their hydrogeologic regimes. Shallow groundwaters in the fractured bedrock are generally dilute (TDS <0.3 g/l), Ca–Na–HCO3 waters and show little indication of mixing with Ca–Mg–HCO3–SO4 groundwater from overburden sediments. The near-modern levels of 3H and 14C, and a warm-climate 2H/18O signature in these groundwaters, indicates that the upper ∼200 m of fractured bedrock contains an active groundwater circulation system with a residence time of tens to hundreds of years. Deeper fracture groundwaters (200–400 m depth) in recharge areas, are more alkaline, Na–Ca–HCO3 waters and evolve to Na–Ca–HCO3–Cl–SO4 waters with increasing distance along the flow path. Isotopic data indicate the presence of a glacial melt-water component suggesting that the residence times of these waters are 103–105 a. These waters form a transition zone between the upper, advective flow regime and a deeper regime in sparsely fractured rock where groundwater in fractures and fracture zones is largely stagnant. At these depths (> 500 m), Na–Ca–Cl–SO4 waters of increasing salinity (up to 50 g/l) with depth are found and in some fractures the waters have evolved to a Ca–Na–Cl composition. Isotopic data indicate that these waters are warm-climate and pre-glacial in origin, with residence times of over 1 Ma. Pore fluids observed to drain from the unfractured rock matrix in the URL facility are almost pure Ca–Cl in composition, ∼90 g/l salinity, and have a 2H/18O composition displaced well to the left of the global meteoric water line, about which all other WRA groundwaters lie. This information indicates that these pore fluids have undergone prolonged water-rock interaction and have residence times of 101–103 Ma. Most of the deeper fracture groundwaters and pore fluids have low Br/Cl ratios and moderate to high δ34S values of dissolved SO4 which indicates that their salinity could be derived from a marine source such as the basinal sedimentary brines and evaporites to the west of the batholith. These fluids may have entered the batholith during early Paleozoic times when sedimentary rocks were deposited over the granite and were driven by a hydraulic gradient resulting from higher ground in western Canada. The hydrogeochemical data and interpretations show that below ∼500 m in the WRA, fracture-hosted groundwaters are very saline, reducing and old, and are, therefore, indicative of stagnant conditions over the period of concern for nuclear waste disposal (1 Ma). The intact rock matrix at these depths is extremely impermeable as indicated by the presence of pore fluids with unusual geochemical and isotopic characteristics. The pore fluids may represent basinal brines that have evolved geochemically and isotopically to their current composition over periods as long as 103 Ma.  相似文献   

19.
The ionic and isotopic compositions (δD, δ18O, and 3H) of urban groundwaters have been monitored in Seoul to examine the water quality in relation to land-use. High tritium contents (6.1–12.0 TU) and the absence of spatial/seasonal change of O–H isotope data indicate that groundwaters are well mixed within aquifers with recently recharged waters of high contamination susceptibility. Statistical analyses show a spatial variation of major ions in relation to land-use type. The major ion concentrations tend to increase with anthropogenic contamination, due to the local pollutants recharge. The TDS concentration appears to be a useful contamination indicator, as it generally increases by the order of forested green zone (average 151 mg/l), agricultural area, residential area, traffic area, and industrialized area (average 585 mg/l). With the increased anthropogenic contamination, the groundwater chemistry changes from a Ca–HCO3 type toward a Ca–Cl(+NO3) type. The source and behavior of major ions are discussed and the hydrochemical backgrounds are proposed as the basis of a groundwater management plan.  相似文献   

20.
Groundwaters from crystalline and metamorphic rocks (hardrocks) and from Quaternary deposits, i.e., alluvial and glacial deposits (softrocks) from the counties of Nord-Trøndelag and Sør-Trøndelag were analyzed for major and minor elements and ions including fluoride. The median concentration of F– in water from the hardrock aquifers is 0.28 mg/l (14.7 eq/l) in contrast to water from softrock aquifers in which it is found to be 0.05 mg/1 (2.6 eq/l). More importantly, ca. 15% of the locations where water was abstracted from hardrock wells contain 1.5 mg/l (78.9 eq/l) F– or more. Thus, 15% of all hardrock wells returned F– results that are at or above the maximum recommended value for drinking water. Of the softrock wells, none are above 1 mg/l. Geologists would normally expect higher F–contents in groundwaters derived from acid rocks, e.g., in granitic or gneissic areas. When comparing the host lithology with the observed F–contents, however, no clear relationship between F– content and lithology is visible. The highest observed F– values actually occur in gneissic host rocks. However, wells drilled in amphibolites/greenstones, mica schists, calcareous rocks, and sedimentary rocks all returned some analytical results above 1.5 mg/l F–. These results suggest that all hardrock wells drilled should be tested for F– and the users informed about the results and advised to take any necessary precautions. When applying the recently proposed Norwegian drinking water limits to our data, 51% of all softrock well waters and 56% of all hardrock well waters are unfit for consumption without prior treatment, although we analyzed only for about half of the proposed elements/parameters. This result seriously questions the concept of fixed action levels—many of them with totally unproven health implications—for so many parameters/elements for hardrock groundwaters.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号