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1.
Major element concentrations, stable (δ18O and δ2H) and radiogenic (3H, 14C) isotopes determined in groundwater provided useful initial tracers for understanding the processes that control groundwater mineralization and identifying recharge sources in semi-arid Cherichira basin (central Tunisia).Chemical data based on the chemistry of several major ions has revealed that the main sources of salinity in the groundwaters are related to the water–rock interaction such as the dissolution of evaporitic and carbonate minerals and some reactions with silicate and feldspar minerals.The stable isotope compositions provide evidence that groundwaters are derived from recent recharge. The δ18O and δ2H relationships implied rapid infiltration during recharge to both the Oligocene and Quaternary aquifers, with only limited evaporation occurring in the Quaternary aquifer.Chemical and isotopic signatures of the reservoir waters show large seasonal evolution and differ clearly from those of groundwaters.Tritium data support the existence of recent recharge in Quaternary groundwaters. But, the low tritium values in Oligocene groundwaters are justified by the existence of clay lenses which limit the infiltration of meteoric water in the unsaturated zone and prolong the groundwater residence time.Carbon-14 activities confirm that groundwaters are recharged from the surface runoff coming from precipitation.  相似文献   

2.
The three-dimensional exposures of the Sierra Blanca marbles and neighbouring rocks in the western Betic cordillera of the south of Spain show tight to isoclinal F3 folds re-folded by a larger sheath-like structure. The relationships between both structures are as follows: (1) The mean axial surface for Sierra Blanca sheath fold can be defined as the great circle of best fit through the ß-axes of sub-cylindrical F3 folding domains. (2) The asymmetric F3-folds indicate a single mainly eastward normal sense of shear. (3) The mean attitude of the axial-plane crenulation foliation, Sc, is also sub-parallel to the mean axial surface for Sierra Blanca sheath fold. The regional context of the Sierra Blanca sheath fold is finally discussed, and a model of a heterogeneous high-strain extensional zone proposed.  相似文献   

3.
This paper records, for the first time, the mineralization of gold (0.98–2.76 ppm) and uranium (133–640 ppm) in marbles from the Arabian-Nubian Shield of the Eastern Desert of Egypt. These auriferous and uraniferous marbles are hosted by sheared and altered ophiolitic serpentinized ultramafic rocks of Gebel El-Rukham (ER), Wadi Daghbag (DG), and Wadi Al Barramiyah (BM). They occur as massive or banded in pod-like or bedded shapes. The ER and BM-mineralized marbles are impure calcitic, whereas the DG marble is impure calcitic to impure dolomitic. Their protolith are pure limestones and dolomitic limestones with probable argillaceous components (BM marble), and their metamorphism (Pan-African) was retrograde. Peaks of metamorphism were at granulite-amphibolite facies for the ER and BM marbles, forming diopside (Al2O3?=?0.17–1.07 wt.%) at 600–900°C and augite (Al2O3?=?2.45–9.40 wt.%) at 825–975°C, and at the amphibolite facies for DG marble, recrystallising the carbonate minerals and forming tremolite. The lowest temperatures of metamorphism were at the upper subgreenschist facies as chlorite (ER and BM marbles) and kaolinite (DG marble) were formed. Metamorphic fluids were, most probably, essentially binary H2O–CO2 mixtures with low NaCl and HF concentrations. Gold in the studied mineralized marbles occurs as native nuggets (10–35 μm) having globule, rod, crescent, and streak shapes, in pores, vugs, and fissures. The source of gold in all marbles is mostly the country ultramafic rocks. Timing of gold mineralization relative to the marblization and metamorphism of the country source ultramafic rocks was both syn- and post-metamorphic. Concerning the ER and DG marbles, it was syn-metamorphic, where Au liberation and transportation were mostly by the metamorphic fluids. The composition and temperature of these fluids were most probably inappropriate for formation of the sulfide complexes of gold. The gold mineralization of BM marble, on the other hand, was mostly post-metamorphic. The mineralising fluid was of surficial origin under oxidizing conditions. The encountered uranium minerals are of secondary origin such as autunite, uranophane, and carnotite. These minerals occur as fine oval aggregates and irregular grains (10–50 μm) usually filling fissures and vugs. The uranium mineralization can be classified as surficial of ages <1.5 Ma. It is proposed that the U was transported from its source (might be flesite and trachyte dikes for the ER and DG marbles and granite rocks for BM marble) to the marble rocks by surface and/or underground water related to the pluvial periods in Egypt. In BM marble, U and Au have mutual mineralizing fluid but different paragenesis.  相似文献   

4.
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   

5.
《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   

6.
The Sierras Pampeanas orogen, in northwestern Argentina, hosts significant Sn–W mineralization in a variety of mostly epizonal granite stocks emplaced in variably metamorphosed country rocks. The San Blas, Huaco and El Durazno granite stocks in the Sierra de Velasco, the La Quebrada granite in the Sierra de Mazán, the Cerro Colorado granite in the Cerro Negro, and the Los Mudaderos and Sauce Guacho granite stocks in the Sierra de Ancasti, are largely peraluminous (ASI between 1.05 and 1.38) and represent S-type granites, are strongly fractionated (i.e., high Rb–Sr ratio), have a low oxidation state (low Fe2O3/Fe2O3 ratio) and are geotectonically linked to syncollisional magmatism. The U–Pb SHRIMP analyses on zircons from the Cerro Colorado and La Quebrada granites, located in the Cerro Negro and Sierra de Mazán, respectively, revealed ages from Lower Ordovician (Tremadocian) to Carboniferous. All granites display elevated LREE values, low HREE values and negative Eu anomalies. With regards to total REE values, two groups of granite stocks can be recognized. The granites with lower REE contents are highly evolved granites and are related to Sn–W mineralization. The mineralized granites display higher values of Sn, W and Rb, and lower values of Sr and Ba compared to barren granites. These trace element characteristics appear to be diagnostic for Sn–W mineralized granite stocks in the western Sierras Pampeanas. The western Sierras Pampeanas contains locally geochemically evolved Carboniferous granites, which are interpreted to be the main control of significant Sn–W mineralization. The Carboniferous age of western Sierras Pampeanas Sn–W mineralization sets it apart from the Triassic age of the Sn–W mineralization in the Eastern Tin belt of Bolivia.  相似文献   

7.
Changes in the climatic conditions during the Late Quaternary and Holocene greatly impacted the hydrology and geochemical evolution of groundwaters in the Great Lakes region. Increased hydraulic gradients from melting of kilometer-thick Pleistocene ice sheets reorganized regional-scale groundwater flow in Paleozoic aquifers in underlying intracratonic basins. Here, we present new elemental and isotopic analyses of 134 groundwaters from Silurian-Devonian carbonate and overlying glacial drift aquifers, along the margins of the Illinois and Michigan basins, to evaluate the paleohydrology, age distribution, and geochemical evolution of confined aquifer systems. This study significantly extends the spatial coverage of previously published groundwaters in carbonate and drift aquifers across the Midcontinent region, and extends into deeper portions of the Illinois and Michigan basins, focused on the freshwater-saline water mixing zones. In addition, the hydrogeochemical data from Silurian-Devonian aquifers were integrated with deeper basinal fluids, and brines in Upper Devonian black shales and underlying Cambrian-Ordovician aquifers to reveal a regionally extensive recharge system of Pleistocene-age waters in glaciated sedimentary basins. Elemental and isotope geochemistry of confined groundwaters in Silurian-Devonian carbonate and glacial drift aquifers show that they have been extensively altered by incongruent dissolution of carbonate minerals, dissolution of halite and anhydrite, cation exchange, microbial processes, and mixing with basinal brines. Carbon isotope values of dissolved inorganic carbon (DIC) range from −10 to −2‰, 87Sr/86Sr ratios range from 0.7080 to 0.7090, and δ34S-SO4 values range from +10 to 30‰. A few waters have elevated δ13CDIC values (>15‰) from microbial methanogenesis in adjacent organic-rich Upper Devonian shales. Radiocarbon ages and δ18O and δD values of confined groundwaters indicate they originated as subglacial recharge beneath the Laurentide Ice Sheet (14-50 ka BP, −15 to −13‰ δ18O). These paleowaters are isolated from shallow flow systems in overlying glacial drift aquifers by lake-bed clays and/or shales. The presence of isotopically depleted waters in Paleozoic aquifers at relatively shallow depths illustrates the importance of continental glaciation on regional-scale groundwater flow. Modern groundwater flow in the Great Lakes region is primarily restricted to shallow unconfined glacial drift aquifers. Recharge waters in Silurian-Devonian and unconfined drift aquifers have δ18O values within the range of Holocene precipitation: −11 to −8‰ and −7 to −4.5‰ for northern Michigan and northern Indiana/Ohio, respectively. Carbon and Sr isotope systematics indicate shallow groundwaters evolved through congruent dissolution of carbonate minerals under open and closed system conditions (δ13CDIC = −14.7 to−11.1‰ and 87Sr/86Sr = 0.7080-0.7103). The distinct elemental and isotope geochemistry of Pleistocene- versus Holocene-age waters further confirms that surficial flow systems are out of contact with the deeper basinal-scale flow systems. These results provide improved understanding of the effects of past climate change on groundwater flow and geochemical processes, which are important for determining the sustainability of present-day water resources and stability of saline fluids in sedimentary basins.  相似文献   

8.
This study presents new data on major, trace and REE element concentration of groundwaters in Lastochka spa located in the northern part of Primorye, Far East of Russia. The studied area is characterized by two types of groundwaters issued from a spring and wells: fresh waters with low mineralization (Total Dissolved Solids is up to 400 mg/l) and high pCO2 waters with high mineralization (TDS is up to 4700 mg/l). New data and previous δ13C(TIC), oxygen (δ18O) and hydrogen (δ2H) isotope data indicate that these waters result from meteoric water infiltration in the Sikhote–Alin mountain, circulating at shallow depths in sedimentary rocks. CO2 in groundwater is of mantle origin.  相似文献   

9.
Groundwater from the major aquifers in southeastern part of Ghana was sampled to determine the main controls on groundwater salinity in the area. This paper uses multivariate statistical methods, conventional graphical methods and stable isotope data to determine spatial relationships among groundwaters from the different hydrogeologic units in the area on the basis of salinity. Q-mode hierarchical cluster analysis (HCA) was used to spatially classify the samples, whilst R-mode factor analysis was used to reduce the dataset into two major principal components representing the sources of variation in the hydrochemistry. Analysis of the major chemical parameters suggests that the principal component responsible for salinity increment in the area is the weathering of minerals in the aquifers. This factor is especially more significant in the upland areas away from the coast. The second factor responsible for salinity in the area is the combined effects of seawater intrusion, and anthropogenic activities. This study finds that four major spatial groundwater groups exist in the area: low salinity, acidic groundwaters which are mainly derived from the Birimian and Togo Series aquifers; low salinity, moderate to neutral pH groundwaters which are mainly from the Voltaian, Buem and Cape Coast granitoids; very high salinity waters which are not suitable for most domestic and irrigation purposes and are mainly from the Keta aquifers; and intermediate salinity groundwaters comprising groundwater from the Keta basin aquifers with minor contributions from the other major terrains. The major water type identified in this study is the Ca–Mg–HCO3 type, which degrades into predominantly Na–Cl–SO4 more saline groundwaters toward the coast. Stable isotope data analyses suggest that groundwater in the Voltaian aquifers is largely of recent meteoric origin. The Birimian and Togo aquifers receive a component of recharge from the tributaries of the Densu and Volta Rivers, after the waters have undergone evaporative enrichment of the heavier isotopes. In the Keta basin, recharge is mainly from precipitation but an observed enrichment of 2H and 18O isotopes is probably due to seawater and evaporative effects since the water table there is very shallow. An analysis of the irrigation quality of groundwater from the six aquifers in the study area using sodium adsorption ratio and electrical conductivity suggests that most of the aquifers supply groundwater of acceptable quality for irrigation. The only exception is the Keta Basin area, where extremely high salinities and SAR values render groundwater from this basin unsuitable for irrigation purposes.  相似文献   

10.
Stable isotopes (δ18O, δ2H and 13C) and radioactivity (3H, 14C) have been used in conjunction with chemical data to evaluate the processes generating the chemical composition, reconstruct the origin of the water and groundwater residence time. The Aleppo basin is comprised of two main limestone aquifers: the first one is unconfined of Paleogene age and the second is confined of Upper Cretaceous age. The chemical data indicate that the dissolution of minerals and evaporation are the main processes controlling groundwater mineralization. The groundwater from the two aquifers is characterized by distinctive stable isotope signatures. This difference in water isotopes is interpreted in terms of difference origin and recharge period. Fresh and brackish shallow groundwater were mostly recharged during the Holocene period. The presence of 3H in several groundwater samples of this aquifer gives evidence that groundwater recharge is going on. Brackish water of the deep confined aquifer has depleted stable isotope composition and very low 14C activity that indicates recharge during the late Pleistocene cold period.  相似文献   

11.
Although shallow groundwater (<50 mbgl) sustains the vast majority of improved drinking-water supplies in rural Africa, there is little information on how resilient this resource may be to future changes in climate. This study presents results of a groundwater survey using stable isotopes, CFCs, SF6, and 3H across different climatic zones (annual rainfall 400–2,000 mm/year) in West Africa. The purpose was to quantify the residence times of shallow groundwaters in sedimentary and basement aquifers, and investigate the relationship between groundwater resources and climate. Stable-isotope results indicate that most shallow groundwaters are recharged rapidly following rainfall, showing little evidence of evaporation prior to recharge. Chloride mass-balance results indicate that within the arid areas (<400 mm annual rainfall) there is recharge of up to 20 mm/year. Age tracers show that most groundwaters have mean residence times (MRTs) of 32–65 years, with comparable MRTs in the different climate zones. Similar MRTs measured in both the sedimentary and basement aquifers suggest similar hydraulic diffusivity and significant groundwater storage within the shallow basement. This suggests there is considerable resilience to short-term inter-annual variation in rainfall and recharge, and rural groundwater resources are likely to sustain diffuse, low volume abstraction.  相似文献   

12.
Atmospheric pollution is one of the main agents of decay in monuments and other works of art located in industrialised urban centres. SO2 is a permanent and abundant component of air pollution and, although it does not have an immediate visual effect, after continuous exposure, it can cause irreversible damage to building materials. Marble is one of the most commonly used ornamental stones in historical monuments and its mineralogical composition makes it very susceptible to damage caused by exposure to SO2. To measure the chemical reactions caused on marble by the action of atmosphere rich in SO2, selected calcitic and dolomitic samples were altered by weathering accelerated test. For this, seven marble types (four calcitic and three dolomitic) were exposed to high concentration of sulphur dioxide for 24 h in a climate chamber under controlled temperature and humidity conditions (20 °C and > 90 % HR). Changes on marble surfaces caused by reactions of SO2 with calcite and dolomite were studied using two non-destructive techniques: chromatic change by means of colorimetry and chemical analysis using X-ray photoelectron spectroscopy (XPS). The development of new mineral phases was also observed by scanning electron microscopy. Colorimetric analysis revealed a decrease in lightness and chromatic parameters suggesting that these changes were due to the development of new mineral phases in all marbles. The XPS technique, which is generally used in the analysis of metals, is relatively new in the field of stone deterioration. It enabled us to recognise the development of sulphites and sulphates on marble surfaces with high precision, after just 24 h of exposure to high SO2 concentrations and to distinguish different decay paths for calcitic and dolomitic marbles.  相似文献   

13.
The compositions of rain, snow, melt, spring and geothermal waters from the rift zone of N.E. Iceland can be explained by seaspray addition, chemical fractionation at the seawater-air interface, burning of fossil fuel, farming activities, purification by partial melting of snow and ice, dissolution of basalts and buffering by alteration minerals. The dissolution of the rocks appears to be incongruent. During solute acquisition, spring compositions move through the stability fields of kaolinite and smectite to the laumontite and illite fields. All but four of the springs are undersaturated with respect to calcite. Silica concentrations are compatible with the solubility of basaltic glass. The reactions reflected in the spring waters appear to have taken place sealed off from atmospheric CO2 after initial saturation.The geothermal waters which are recharged by the spring waters are depleted in Mg and Ca but enriched in carbon and sulfur with respect to dissolution of primary rocks. Expressions are derived relating dissolution rates of rocks, age of groundwaters, physical properties of groundwaters and mass transfer. The characteristic rock particle radii in the cold water aquifers range from 0.2 to 2 cm and the characteristic crack openings are of the order 0.04 to 0.4 cm. Using laboratory studies on the Icelandic lavas as a guide, the residence times of the cold waters in the aquifers can be estimated at 60 days to 4 years. The average active surface area of the aquifers enclosing 1000 g of spring water is of the order of 0.6 to 6 m2 and these 1000 g of water have reacted with 0.1 to 1 g of basaltic rocks. The same mass of thermal water has interacted with 100 to 300 g of unaltered rocks.  相似文献   

14.
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   

15.
《Ore Geology Reviews》2003,22(1-2):17-39
Many talc deposits occur in the Hwanggangri Mineralized Zone (HMZ) in dolomitic marbles of the Cambro-Ordovician Samtaesan Formation within 1 km of the contact with the Cretaceous Muamsa Granite. Talc commonly forms fine-grained, fibrous aggregates, or pseudomorphs after tremolite; abundant tremolite is included as impurities in the talc ore. Talc generally was derived from tremolite in calc-silicate rock within the dolomitic marble. Calc-silicate rock, consisting mainly of tremolite and diopside, was generated from silicic metasomatism during the prograde stage, which promoted decarbonation reactions until dolomite was exhausted locally. Hydrothermal alteration of calc-silicate rock to talc is marked by the addition of Mg and Si, and the leaching of Ca; Cr, Co, and Ni were relatively immobile during the retrograde stage. Contact metamorphism related to the granite intrusion generated the successive appearance of tremolite, diopside, and forsterite, or wollastonite-bearing assemblages in the marble, depending on the bulk rock composition. The XCO2 content of the metamorphic fluids rose initially above XCO2=0.6, and decreased steadily toward a water-rich composition with increasing temperature above 600 °C in the calcitic marble, while buffered reaction of the dolomitic marble occurred at higher XCO2 conditions above 600 °C. Talc mineralization developed under metastable conditions with infiltration of large amounts of igneous fluids along a fault-shattered zone during the retrograde stage and is characterized by the loss of Ca2+ with the addition of Mg2+. Oxygen and carbon isotopic variations of carbonate and calc-silicate minerals are in agreement with theoretical relationships determined for decarbonation products of contact metamorphism. Talc formation temperatures obtained from oxygen isotope fractionation, T–XCO2 relationships, and activity diagrams range from 380 to 400 °C.  相似文献   

16.
《Applied Geochemistry》1998,13(5):593-606
The comparative geochemical and isotopic study of confined and unconfined Chalk groundwaters of the Paris Basin and the N German Basin proves a significant chemical evolution during groundwater flow from the recharge zones to the deep confined aquifer. Different time dependent geochemical parameters have been tested as dating tools: Cation ratios (Sr2+/Ca2+, Mg2+/Ca2+), N–NO−3, noble gas contents as paleotemperature indicators (Ne, Ar, Kr, Xe), radiogenic He, 13C, 14C, 18O, 2H, 3H. Cation ratios and 13C show the importance of incongruent dissolution processes in the Chalk aquifer. Water–rock interactions were taken into account in a multi-step dissolution model to determine radiocarbon groundwater ages. The oldest waters in the confined part of the Paris basin Chalk with maximum 14C ages of 14,000 a B.P. contain pleistocene recharge components as can be shown by a stable isotope depletion and noble gas temperatures significantly lower than in recent groundwaters. Chalk waters at the Lägerdorf site in Northern Germany show a distinct stratification with respect to residence times and hydrochemistry.  相似文献   

17.
Whole-rock geochemical analyses using major and trace elements in combination with the Sm–Nd and Pb–Pb isotope systems, together with SHRIMP age dating on metasedimentary rocks from the Sierras de Chepes, the Sierras de Córdoba, the Sierra Norte and the San Luis Formation in the Sierra de San Luis, have been carried out to unravel the provenance and the geodynamic history of the Eastern Sierras Pampeanas, Central Argentina. The geochemical and the Sm–Nd data point to a slightly stronger mafic and less-fractionated material in the provenance area of the Sierras de Córdoba when compared to the other units. The TDM model ages from the Sierras de Chepes (~1.82 Ga) and the Sierra Norte (~1.79 Ga) are significantly older than the data from the Sierras de Córdoba (1.67 Ga). The Pb data are homogeneous for the different units. Only the 208Pb/204Pb ratios of some samples from the Sierras de Córdoba are higher. A late Pampean detrital zircon peak around 520 Ma from the Sierras de Chepes is in accordance with the new data from the San Luis Formation. This is similar to the literature data from the Famatina Belt located to the northwest of the Sierras de Chepes and also fits the detrital zircon peaks in the Mesón group. These maximum depositional ages were also reported from some locations in the Puncoviscana Formation but are absent in the Sierras de Córdoba. An improved model for the development of the Eastern Sierras Pampeanas in the area between the Sierras de Córdoba and the Puncoviscana Formation is provided. This gives new insights into the late Pampean development of the Sierra de San Luis and the complex development of the Eastern Sierras Pampeanas. This new model explains the younger detrital ages in the Puncoviscana Formation compared with the older ages of the Sierras de Córdoba. Another model of the Sierra de San Luis explains the younger depositional ages of the Pringles Metamorphic Complex and the San Luis Formation when compared to the Nogolí Metamorphic Complex and the Conlara Metamorphic Complex. Additionally, the rather fast change of the high-grade metamorphic conditions in the Pringles Metamorphic Complex and the low-grade metamorphic conditions in the San Luis Formation is explained by extension, the ascent of (ultra) mafic material and later folding and erosion.  相似文献   

18.
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   

19.
《Applied Geochemistry》1987,2(4):417-426
This paper discusses the geochemistry, origin and evolution of groundwaters in the Lode`ve Basin Massif Central, France, including major and trace elements (U, Ra, Ba and Fe) and the significance of the redox potential. These groundwaters originate from thermal waters by CO2 outgassing and mixing with meteoric waters. The measured redox potential (Eh > −50 mV) is generally controlled by the ferric oxide-Fe2+ equilibrium; below this potential the groundwaters are saturated with respect to FeS.Redox systems other than Fe are not necessarily at equilibrium, and this is particularly true for U. In the relatively reduced waters (Eh< 100mV), U concentrations may be controlled by coffinite or uraninite. Above 100 mV, U concentrations range from 10 to 200 ppb; they correspond either to mineral dissolution, or could be controlled by an oxidized mineral.Radium mobility is strongly dependent on SO4 concentration, and it coprecipitates with barite. Radium probably has its origin in calcium-sodium bicarbonate type waters and is not related to U mineralization.  相似文献   

20.
The Salumber-Ghatol belt in Rajasthan, India, situated along southern margin of the Aravalli Craton, hosts a cluster of Cu-Au deposits in calcitic and dolomitic marbles that belong to Debari Group of the Paleo-mesoproterozoic Aravalli Supergroup. The Fe-Mn rich dolomitic marble of the Delwara Formation hosts Cu-Au-Fe-oxide mineralization at Ghagri and associated distal K-Fe-Mg rich altered rocks (cryptocrystalline microcline + magnesioriebeckite + magnetite + phlogopite) and proximal feldspathised carbonate rocks (medium grained albite + microcline + dolomite + magnetite). The calcitic marble of Mukandpura Formation hosts Dugocha Cu-Au deposit with development of distal graphitetourmaline-bearing albitites and proximal albite-microcline-magnetite rocks. Calcite and dolomite carbonates of Bhukia region with development of albite-actinolite-bearing alteration assemblages host the largest of the Cu-Au deposits in this belt. The second generation folds and associated ductile-brittle shear zones of the multiply deformed events constitute conduits for the mineralizing fluids at all locations in this belt.  相似文献   

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