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1.
Many cities around the world are developed at alluvial fans. With economic and industrial development and increase in population, quality and quantity of groundwater are often damaged by over-exploitation in these areas. In order to realistically assess these groundwater resources and their sustainability, it is vital to understand the recharge sources and hydrogeochemical evolution of groundwater in alluvial fans. In March 2006, groundwater and surface water were sampled for major element analysis and stable isotope (oxygen-18 and deuterium) compositions in Xinxiang, which is located at a complex alluvial fan system composed of a mountainous area, Taihang Mt. alluvial fan and Yellow River alluvial fan. In the Taihang mountainous area, the groundwater was recharged by precipitation and was characterized by Ca–HCO3 type water with depleted δ18O and δD (mean value of −8.8‰ δ18O). Along the flow path from the mountainous area to Taihang Mt. alluvial fan, the groundwater became geochemically complex (Ca–Na–Mg–HCO3–Cl–SO4 type), and heavier δ18O and δD were observed (around −8‰ δ18O). Before the surface water with mean δ18O of −8.7‰ recharged to groundwater, it underwent isotopic enrichment in Taihang Mt. alluvial fan. Chemical mixture and ion exchange are expected to be responsible for the chemical evolution of groundwater in Yellow River alluvial fan. Transferred water from the Yellow River is the main source of the groundwater in the Yellow River alluvial fan in the south of the study area, and stable isotopic compositions of the groundwater (mean value of −8.8‰ δ18O) were similar to those of transferred water (−8.9‰), increasing from the southern boundary of the study area to the distal end of the fan. The groundwater underwent chemical evolution from Ca–HCO3, Na–HCO3, to Na–SO4. A conceptual model, integrating stiff diagrams, is used to describe the spatial variation of recharge sources, chemical evolution, and groundwater flow paths in the complex alluvial fan aquifer system.  相似文献   

2.
On the basis of the hydrogeology of the Dousitu River drainage basin, the changes of water flow rate, δ18O and δD along the Dousitu River are discussed according to measured and analytical results. Changes of flow rate along the Dousitu River agree well with groundwater level contours and the recharge and discharge of groundwater to the river. When compared with other types of water in the area, it is obvious that the 18O and D of river waters have experienced evaporation. The changes of δ18O and δD along the Dousitu River are mainly caused by combined effects of groundwater recharge and river water evaporation. The recharge of groundwater makes δ18O and δD of the river water decrease. Evaporation makes δ18O and δD of the river water increase. The evaporation fractions of the river water are calculated using the kinetic fractionation theory. Results showed as much as 10–30% of water was evaporated in different segments of Dousitu River.  相似文献   

3.
The source of metasomatic fluids in iron-oxide–copper–gold districts is contentious with models for magmatic and other fluid sources having been proposed. For this study, δ 18O and δ 13C ratios were measured from carbonate mineral separates in the Proterozoic eastern Mt Isa Block of Northwest Queensland, Australia. Isotopic analyses are supported by petrography, mineral chemistry and cathodoluminescence imagery. Marine meta-carbonate rocks (ca. 20.5‰ δ 18O and 0.5‰ δ 13C calcite) and graphitic meta-sedimentary rocks (ca. 14‰ δ 18O and −18‰ δ 13C calcite) are the main supracrustal reservoirs of carbon and oxygen in the district. The isotopic ratios for calcite from the cores of Na–(Ca) alteration systems strongly cluster around 11‰ δ 18O and −7‰ δ 13C, with shifts towards higher δ 18O values and higher and lower δ 13C values, reflecting interaction with different hostrocks. Na–(Ca)-rich assemblages are out of isotopic equilibrium with their metamorphic hostrocks, and isotopic values are consistent with fluids derived from or equilibrated with igneous rocks. However, igneous rocks in the eastern Mt Isa Block contain negligible carbon and are incapable of buffering the δ 13C signatures of CO2-rich metasomatic fluids associated with Na–(Ca) alteration. In contrast, plutons in the eastern Mt Isa Block have been documented as having exsolved saline CO2-rich fluids and represent the most probable fluid source for Na–(Ca) alteration. Intrusion-proximal, skarn-like Cu–Au orebodies that lack significant K and Fe enrichment (e.g. Mt Elliott) display isotopic ratios that cluster around values of 11‰ δ 18O and −7‰ δ 13C (calcite), indicating an isotopically similar fluid source as for Na–(Ca) alteration and that significant fluid–wallrock interaction was not required in the genesis of these deposits. In contrast, K- and Fe-rich, intrusion-distal deposits (e.g. Ernest Henry) record significant shifts in δ 18O and δ 13C towards values characteristic of the broader hostrocks to the deposits, reflecting fluid–wallrock equilibration before mineralisation. Low temperature, low salinity, low δ 18O (<10‰ calcite) and CO2-poor fluids are documented in retrograde metasomatic assemblages, but these fluids are paragenetically late and have not contributed significantly to the mass budgets of Cu–Au mineralisation.  相似文献   

4.
Hydro- and isotope geochemistry are used to refine groundwater conceptual models in two areas of central Italy (Acque Albule Basin and Velino River Valley) affected by extensional Quaternary tectonics, where deep and shallow groundwater flow systems are interacting. The role of geology, of recent deposits filling the plains and of main tectonic features controlling groundwater flowpaths and deep-seated fluids emergences are investigated and discussed. Environmental isotopes (2H and 18O) confirm recharge in the surrounding carbonate aquifers, and meteoric origin of both shallow and deep groundwater. Major ion chemistry indicates a mixing between shallow Ca-HCO3 groundwater from carbonate aquifers and deep Ca-HCO3-SO4 groundwater, characterised by higher salinity and temperature and high concentration in sulphates. Isotopic composition of dissolved sulphates (δ 34S and δ 18O) and dissolved inorganic carbon (δ 13C), henceforth indicated as DIC, are used to verify the presence of different sources of groundwater, and to validate the mixing model suggested by the major ion analyses. Sulphate isotope composition suggests a marine origin for the groundwater characterised by elevated sulphate concentration, whose source is present in the deep buried sequences. Carbon isotope composition confirms the role of a DIC source associated to CO2 degassing of a deep reservoir. Groundwater conceptual models are improved underlining the importance of Plio-Pleistocene sequences filling the tectonic depression. In the Acque Albule area, the travertine plateau represents a mixing stratified aquifer, where deep groundwater contribution is spread into the shallow aquifer. The alluvial–clastic–lacustrine leaky aquifer of Velino Valley enables a complete mixing of shallow and deep groundwater allowing spot-located discharge of deep groundwater along tectonic patterns and facilitating sulphate reduction in the lacustrine sediments, explaining locally the presence of H2S.  相似文献   

5.
The need for more agricultural or residential land has encouraged reclamation at the coastal areas of Korea since 1200 ad (approximately). The groundwaters of these reclaimed areas could be expected to reveal hydrogeochemical properties different from those of areas directly affected by seawater intrusion. The purpose of this study, therefore, was to examine the salinization of shallow groundwater in a coastal reclaimed area and to identify the effect of land reclamation on groundwater quality. Major cations and anions, iodide, total organic carbon, δD, δ 18O and δ 13C were measured to assist the hydrogeochemical analysis. Chloride, δD and δ 18O data clearly show that the Na–Cl type water results from mixing of groundwater with seawater. In particular, the δD and δ 18O of Ca+Mg–Cl+NO3 type groundwaters are close to the meteoric water line, but Na–Cl type waters enriched in chloride are 18O-enriched with respect to the meteoric water line. Meanwhile, carbon isotopic data and I/Cl ratios strongly suggest that there are various sources of salinity. The δ 13C values of Na–Cl type groundwaters are generally similar to those of Ca+Mg–Cl+NO3 type waters, which are depleted in 13C with respect to seawater. I/Cl ratios of Na–Cl type groundwater are 10–100 times higher than that of seawater. Because the reclamation has incorporated a large amount of organic matter, it provides optimum conditions for the occurrence of redox processes in the groundwater system. Therefore, the salinization of groundwater in the study area seems to be controlled not only by saltwater intrusion but also by other effects, such as those caused by residual salts and organic matter in the reclaimed sediments.  相似文献   

6.
Klyuchevskoy volcano, in Kamchatka’s subduction zone, is one of the most active arc volcanoes in the world and contains some of the highest δ18O values for olivines and basalts. We present an oxygen isotope and melt inclusion study of olivine phenocrysts in conjunction with major and trace element analyses of 14C- and tephrochronologically-dated tephra layers and lavas spanning the eruptive history of Klyuchevskoy. Whole-rock and groundmass analyses of tephra layers and lava samples demonstrate that both high-Mg (7–12.5 wt% MgO) and high-Al (17–19 wt% Al2O3, 3–6.5 wt% MgO) basalt and basaltic andesite erupted coevally from the central vent and flank cones. Individual and bulk olivine δ18O range from normal MORB values of 5.1‰ to values as high as 7.6‰. Likewise, tephra and lava matrix glass have high-δ18O values of 5.8–8.1‰. High-Al basalts dominate volumetrically in Klyuchevskoy’s volcanic record and are mostly high in δ18O. High-δ18O olivines and more normal-δ18O olivines occur in both high-Mg and high-Al samples. Most olivines in either high-Al or high-Mg basalts are not in oxygen isotopic equilibrium with their host glasses, and Δ18Oolivine–glass values are out of equilibrium by up to 1.5‰. Olivines are also out of Fe–Mg equilibrium with the host glasses, but to a lesser extent. Water concentrations in olivine-hosted melt inclusions from five tephra samples range from 0.4 to 7.1 wt%. Melt inclusion CO2 concentrations vary from below detection (<50 ppm) to 1,900 ppm. These values indicate depths of crystallization up to ~17 km (5 kbar). The variable H2O and CO2 concentrations likely reflect crystallization of olivine and entrapment of inclusions in ascending and degassing magma. Oxygen isotope and Fe–Mg disequilibria together with melt inclusion data indicate that olivine was mixed and recycled between high-Al and high-Mg basaltic melts and cumulates, and Fe–Mg and δ18O re-equilibration processes were incomplete. Major and trace elements in the variably high-δ18O olivines suggest a peridotite source for the parental magmas. Voluminous, highest in the world with respect to δ18O, and hydrous basic volcanism in Klyuchevskoy and other Central Kamchatka depression volcanoes is explained by a model in which the ascending primitive melts that resulted from the hydrous melt fluxing of mantle wedge peridotite, interacted with the shallow high-δ18O lithospheric mantle that had been extensively hydrated during earlier times when it was part of the Kamchatka forearc. Following accretion of the Eastern Peninsula terrains several million years ago, a trench jump eastward caused the old forearc mantle to be beneath the presently active arc. Variable interaction of ascending flux-melting-derived melts with this older, high-δ18O lithospheric mantle has produced mafic parental magmas with a spectrum of δ18O values. Differentiation of the higher δ18O parental magmas has created the volumetrically dominant high-Al basalt series. Both basalt types incessantly rise and mix between themselves and with variable in δ18O cumulates within dynamic Klyuchevskoy magma plumbing system, causing biannual eruptions and heterogeneous magma products. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

7.
Discovery of high contents of methane gas in coals of the Mist Mountain Formation in the Elk River valley, southeastern British Columbia, Canada, has led to increased exploration activity for coal-seam gas (CSG). CSG production requires groundwater abstraction to depressurize the coal beds and to facilitate methane flow to the production wells. Groundwater abstraction will have hydrodynamic effects on the flow system, and an understanding of the groundwater flow system is needed to evaluate these effects. The purpose of this paper is to describe the groundwater flow system in the area by means of a groundwater flow model and interpretation of hydrochemical and isotopic analyses of groundwater and surface water. Groundwater flow for the Weary Creek exploration area is modeled in two vertical sections. The model domains, based on classic upland–lowland conceptual flow models, are approximately 10,000 m long and 4,000 m deep. Each consists of a fixed water-table boundary and no-flow boundaries along the traces of major faults. Steady-state groundwater flow is calibrated to hydraulic-head, streamflow, and groundwater-recharge data. Simulated steady-state velocity fields define regional and local flow components consistent with the conceptual model. The results are consistent with regional trends in δ2H, δ18O, tritium, and TDS, which define two distinct groundwater groups (A and B) and a third of intermediate composition. An active, shallow, local flow component (group A) is recharged in beds cropping out along subdued ridges; this component discharges as seeps along lower and mid-slope positions in the southern part of the study area. The waters are tritiated, relatively enriched in δ2H and δ18O, and have low TDS. A deeper regional flow component (group B), which originates at a higher altitude and which discharges to the Elk River valley bottom, is characterized by non-tritiated groundwater with relatively depleted δ2H and δ18O, and higher TDS. Groundwater contributes less than 10% of the total direct flow to the Elk River, as indicated by flow measurements and by the absence of group A and group B characteristics in the river water. Thus it is hypothesized that groundwater extraction during CSG production will have little impact on the river. The groundwater flow model developed in this work is used in a companion paper to further test this hypothesis. Electronic Publication  相似文献   

8.
Deuterium, δ 18O, major ions and dissolved silica in groundwater from semi-arid Mayo-Tsanaga river basin in the Far North Province, Cameroon were used to trace hydrogeochemical processes that control their concentrations and to explore for usability of the water. Electrical conductivity ranges from 57–2,581 μs/cm with alternating low and high values along the hydraulic gradient. Waters from piedmont alluvium show low concentrations in major cations, which peak in Mg within basalt, Na within plain alluvium, and Ca within basalt and the sandy Limani-Yagoua ridge. The initial dominant groundwater composition is CaHCO3, which did not evolve within the basalt and piedmont alluvium, but evolved to NaHCO3 in the granite and plain alluvium. The main processes controlling the major ions composition include the following: (1) dissolution of silicates and fluorite; (2) precipitation of fluorite and carbonate; (3) cation exchange of Ca in water for Na in clay; (4) and anthropogenic activities. The δD and δ 18O ratios vary from −35 to 0.7 and −5.3 to 1.1‰, respectively. The lowest and highest isotope ratios are observed in groundwater within the downstream sandy Limani-Yagoua ridge and the upstream graintes respectively. Variation in isotope ratios depends on altitude effect of −0.48‰ per 100 m between 600 and 850 m asl, and on evaporation, which had insignificant effect on the water salinity. Seventy percent of the groundwater shows poor drinking quality and 90% is suitable for irrigation. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

9.
Evolution of the shallow groundwater quality under saline intrusion in porous aquifer system has been studied with environmental isotopes and geochemistry in the Laizhou Bay area, China. Two campaigns of water sampling from various sources were carried out in spring and winter for environmental isotopic and chemical analyses. The origin of groundwater salinity from intrusion of both modern seawater and deep brine water was identified by analysing the correlations between 18O, D, T, Cl−, SO42− and electrical conductivity. The results indicate that the brine is originated from evaporating and concentrating of intruded seawater and its δD and δ18O are different from modern seawater but similar to those of mixture of seawater with fresh groundwater. It is hard to distinguish the salinity origin in this area by the δD–δ18O relationship alone. The relations between δ18O and conductivity, Cl− and SO42− have been used to identify the salinity origin due to the distinct difference in salinity between the brine and seawater, conjunctively with use of T. A threshold of T = 12 TU was adopted to identify the origin of saline groundwater.  相似文献   

10.
Unplanned exploitation of groundwater constitutes emerging water-related threats to MayoTsanaga River Basin. Shallow groundwater from crystalline and detrital sediment aquifers, together with rain, dams, springs, and rivers were chemically and isotopically investigated to appraise its evolution, recharge source and mechanisms, flow direction, and age which were used to evaluate the groundwater susceptibility to contamination and the basin’s stage of salinization. The groundwater which is Ca–Na–HCO3 type is a chemically evolved equivalent of surface waters and rain water with Ca–Mg–Cl–SO4 chemistry. The monsoon rain recharged the groundwater preferentially at an average rate of 74 mm/year, while surface waters recharge upon evaporation. Altitude effect of rain and springs show a similar variation of −0.4‰ for δ18O/100 m, but the springs which were recharged at 452, 679, and 773 m asl show enrichment of δ18O through evaporation by 0.8‰ corresponding to 3% of water loss during recharge. The groundwater which shows both local and regional flow regimes gets older towards the basins` margin with coeval enrichment in F− and depletion in NO3 −. Incidentally, younger groundwaters are susceptible to anthropogenic contamination and older groundwaters are sinks of lithologenic fluoride. The basins salinization is still at an early stage.  相似文献   

11.
Measurements were made of sulphur and oxygen isotope ratios of sulphate in some Slovenian rivers, lakes and tap waters. δ34S ranged from −0.2 to + 13.3‰, δ18O ranged from +4.9 to + 13.6‰, and the sulphate content varied from 0.8 to 41.4 mg/L. Rivers flowing from the Julian Alps contain a very low amount of sulphate that is leached from a thin horizon of soil by rain. As confirmed by their low δ18O values, these sulphates do not enter the rivers directly in rain, but arise from biochemical cycling in the soil. The low δ34S of this sulphate indicates that it originates from the oxidation of sedimentary sulphides. The evolution of sulphates along the river course was investigated for the Sava and Ljubljanica rivers. The variations observed in sulphate from the waters studied result from variations in the contribution of sulphates of different origin. Downstream the Sava River sulphate is depleted in the heavy isotopes of both sulphur and oxygen, with δ-values gradually tending toward the δ-values of groundwater sulphates in the watershed. In contrast, the δ-values of sulphate in the Ljubljanica River are almost constant and similar to those of sulphate in local groundwater. Introduction of water from Italian and Slovenian mines was recorded in the Soča River, where the lowest δ34S value of sulphate sulphur (−0.2‰) was observed. In addition, the influence of sulphate from the oxidation of sedimentary sulphides was recorded in the Sotla River. No evidence was found for introduction of sulphate from factories.  相似文献   

12.
The concentrations of CH4, SO42−, σCO2 and the carbon isotope compositions of ΣCO2 and CH4 in the pore-water of the GS sedimentary core collected from Guishan Island (Pearl River Estuary), South China Sea, were determined. The methane concentration in the pore-water shows dramatic changes and sulfate concentration gradients are linear at the base of the sulfate reduction zone for the station. The carbon isotope of methane becomes heavier at the sulfate-methane transition (SMT) likely because of the Raleigh distillation effect; 12CH4 was oxidized faster than 13CH4, and this caused the enrichment of residual methane δ 13C and δ 13C-ΣCO2 minimum. The geochemical profiles of the pore-water support the existence of anaerobic oxidation of methane (AOM), which is mainly controlled by the quality and quantity of the sedimentary organic matter. As inferred from the index of δ 13C-TOC value and TOC/TN ratio, the organic matter is a mix of mainly refractory terrestrial component plus some labile alga marine-derived in the study area. A large amount of labile organic matter (mainly labile alga marine-derived) is consumed via the process of sedimentary organic matter diagenesis, and this reduces the amount of labile organic matter incorporated into the base of the sulfate reduction zone. Due to the scarcity of labile organic matter, the sulfate will in turn be consumed by its reaction with methane and therefore AOM takes place. Based on a diffussion model, the portion of pore-water sulfate reduction via AOM is 58.6%, and the percentage of ΣCO2 in the pore-water derived from AOM is 41.4%. Thus, AOM plays an important role in the carbon and sulfur cycling in the marine sediments of Pearl River Estuary.  相似文献   

13.
Isotopes of deuterium and oxygen-18 in thermal groundwater in China   总被引：1，自引：0，他引：1  
Compositions of deuterium and 18O isotopes of 90 representative samples indicate that thermal groundwater in most parts of China is meteoric in origin. Latitude, altitude, and continent effects have significant bearing on the values of δD and δ18O of the hot water samples. Oxygen-18 shift is not significant in most of the thermal groundwater, especially the hot water of low-to-moderate temperature. Slight oxygen-18 shift is only found in some hot springs of high temperature in Tibet and western Yunnan and in thermal groundwater of low-to-moderate temperature in the deep-seated carbonate aquifers in the northern North China Plain (including the Tianjin area). Near-surface boiling may causes the shift of the former and the latter may be attributed to exchange of oxygen-18 between water and carbonates in the geothermal systems of taphrogenic basin-type. Hot springs in Tibet and western Sichuan have very low contents of δD and δ18O, possibly due to recharge of precipitation and snow-melting water of extremely depleted δD and δ18O values at high latitudes of several thousands of meters.  相似文献   

14.
Stable isotopes of H2O are used to define the hyporheic–hypolentic boundary in Ledbetter Creek as it discharges to Kentucky Lake, a constructed reservoir in western Kentucky, USA. High-resolution (centimeter-scale) sample collection and analysis were utilized to determine one-dimensional variations in δ2H and δ18O of H2O and chloride (Cl−) across the boundary. During reservoir low stand in winter, the hyporheic–hypolentic zone contains water from Ledbetter Creek and groundwater separated by an interface at ~10 cm below the channel bottom. Following reservoir-stage increase in spring and summer, water from Kentucky Lake infiltrates into the hyporheic–hypolentic zone to a depth of at least 18 cm below the channel bottom. Reservoir-stage decline in autumn causes source-water mixing, largely obscuring the hyporheic–hypolentic boundary. Stable isotopes provide an effective complement to conventional tracers for delineation of water masses within the hyporheic–hypolentic zone.
Resumen Se han utilizado isótopos estables del agua para definir el límite hiporreico-hipoléntico en Ledbetter Creek, que constituye una zona de descarga del lago Kentucky, una presa construida al Oeste de Kentucky, USA. Se ha llevado a cabo una recogida de muestras de alta resolución (a escala centimétrica) y se utilizaron los resultados para determinar las variaciones unidimensionales en δ2H y δ18O del H2O y los cloruros (Cl−) alrededor del límite. Durante la época de niveles bajos en invierno, la zona hiporreica-hipolentica tiene agua procedente de Ledbetter Creek y de agua subterránea separada por una interfase de ~10 cm debajo del límite del canal. Siguiendo el incremento de los niveles en la presa en primavera y verano, el agua del Lago Kentucky se infiltra en la zona hiporreica-hipoléntica hasta una profundidad de, al menos, 18 cm bajo el límite hiporreico-hipoléntico. Los isótopos estables aportan un complemento efectivo a los trazadores convencionales para la delimitación de masas de agua dentro de la zona hiporreica-hipoléntica.
Résumé L’utilisation des isotopes stables de la molécule d’eau a permis de définir l’interface hyporhéique-hypolentique dans la Ledbetter Creek, au point de déversement dans le réservoir artificiel que constitue le Kentucky Lake (Ouest du Kentucky, Etats-Unis). Une campagne de prélèvements à haute résolution (échelle centimétrique) a contribué à déterminer les variations unidimensionnelles des valeurs de δ2H et de δ18O de la molécule d’eau et de la concentration en chlorures (Cl−) de part et d’autre de l’interface. En hiver, lorsque le niveau du réservoir est minimal, la zone hyporhéique-hypolentique contient de l’eau de la Ledbetter Creek et de l’eau souterraine, séparées par un interface situé environ 10 cm sous le fond du chenal. Suite aux recharges printanières et estivales, l’eau du Kentucky Lake envahit la zone hyporhéique-hypolentique sur plus de 18 cm sous le fond du chenal. En automne, la baisse de niveau dans le réservoir occasionne un mélange des eaux, rendant diffus l’interface hyporhéique-hypolentique. Les isotopes stables constituent ainsi un complément efficace aux traceurs conventionnels pour la délimitation des masses d’eau dans la zone hyporhéique-hypolentique.
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15.
At Sams Creek, a gold-bearing, peralkaline granite porphyry dyke, which has a 7 km strike length and is up to 60 m in thickness, intrudes camptonite lamprophyre dykes and lower greenschist facies metapelites and quartzites of the Late Ordovician Wangapeka formation. The lamprophyre dykes occur as thin (< 3 m) slivers along the contacts of the granite dyke. δ18Omagma values (+5 to +8‰, VSMOW) of the A-type granite suggest derivation from a primitive source, with an insignificant mature crustal contribution. Hydrothermal gold–sulphide mineralisation is confined to the granite and adjacent lamprophyre; metapelite country rocks have only weak hydrothermal alteration. Three stages of hydrothermal alteration have been identified in the granite: Stage I alteration (high fO2) consisting of magnetite–siderite±biotite; Stage II consisting of thin quartz–pyrite veinlets; and Stage III (low fO2) consisting of sulphides, quartz and siderite veins, and pervasive silicification. The lamprophyre is altered to an ankerite–chlorite–sericite assemblage. Stage III sulphide veins are composed of arsenopyrite + pyrite ± galena ± sphalerite ± gold ± chalcopyrite ± pyrrhotite ± rutile ± graphite. Three phases of deformation have affected the area, and the mineralised veins and the granite and lamprophyre dykes have been deformed by two phases of folding, the youngest of which is Early Cretaceous. Locally preserved early-formed fluid inclusions are either carbonic, showing two- or three-phases at room temperature (liquid CO2-CH4 + liquid H2O ± CO2 vapour) or two-phase liquid-rich aqueous inclusions, some of which contain clathrates. Salinities of the aqueous inclusions are in the range of 1.4 to 7.6 wt% NaCl equiv. Final homogenisation temperatures (Th) of the carbonic inclusions indicate minimum trapping temperatures of 320 to 355°C, which are not too different from vein formation temperatures of 340–380°C estimated from quartz–albite stable isotope thermometry. δ18O values of Stage II and III vein quartz range from +12 and +17‰ and have a bimodal distribution (+14.5 and +16‰) with Stage II vein quartz accounting for the lower values. Siderite in Stage III veins have δ18O (+12 to +16‰) and δ13C values (−5‰, relative to VPDB), unlike those from Wangapeka Formation metasediments (δ13Cbulk carbon values of −24 to −19‰) and underlying Arthur Marble marine carbonates (δ18O = +25‰ and δ13C = 0‰). Calculated δ18Owater (+8 to +11‰, at 340°C) and (−5‰) values from vein quartz and siderite are consistent with a magmatic hydrothermal source, but a metamorphic hydrothermal origin cannot be excluded. δ34S values of sulphides range from +5 to +10‰ (relative to CDT) and also have a bimodal distribution (modes at +6 and +9‰, correlated with Stage II and Stage III mineralisation, respectively). The δ34S values of pyrite from the Arthur Marble marine carbonates (range from +3 to +13‰) and Wangapeka Formation (range from −4 to +9.5‰) indicate that they are potential sources of sulphur for sulphides in the Sams Creek veins. Another possible source of the sulphur is the lithospheric mantle which has positive values up to +14‰. Ages of the granite, lamprophyre, alteration/mineralisation, and deformation in the region are not well constrained, which makes it difficult to identify sources of mineralisation with respect to timing. Our mineralogical and stable isotope data does not exclude a metamorphic source, but we consider that the source of the mineralisation can best be explained by a magmatic hydrothermal source. Assuming that the hydrothermal fluids were sourced from crystallisation of the Sams Creek granite or an underlying magma chamber, then the Sams Creek gold deposit appears to be a hybrid between those described as reduced granite Au–Bi deposits and alkaline intrusive-hosted Au–Mo–Cu deposits.  相似文献   

16.
The aim of the paper is to understand the geological control of groundwater, the recharge sources, the relative age of groundwater and the interaction between surface water and groundwater of the southwestern part of North Bengal Plain in the alluvium filled gap between the Rajmahal hills on the west and the Garo hills on the east. The area is covered by Quaternary alluvia of two different ages, viz. the Older Alluvium and the Newer Alluvium. The Older Alluvium of Pleistocene age is made up of argillaceous bed reddish brown in color and interspread with ‘kankar’ and laterite debris and the Newer Alluvium is dark, loosely compacted and has a high moisture content. A hydrostarigraphic model of the top 120 m geological column has been built by direct field observation, constructing Fence diagram, lithofacies and isotope analyses. The model indicates an oscillating environment of deposition of sediments from bottom to top with oxidizing at the bottom followed by reducing and then oxidizing environment at the top. The hydrogeochemistry of groundwater also suggests a predominantly reducing condition of the aquifer with high HCO3 −, low SO4 2− and NO3 − concentrations. The shallow groundwater at places contains heavy metals such as copper, cadmium, manganese, iron, chromium and arsenic. The δ18O and tritium values of groundwater are within the range of monsoon precipitation composition which indicates that groundwater is probably recharged primarily from precipitation. The plots of δ18O and δD show slight deviation from the Local Mean Water Lines suggesting that some evaporation of rainfall occurs prior to or during infiltration. Therefore groundwater occurs under unconfined condition. Lithofacies analysis indicates that the sediments below the depth of 40 m are the potential water bearing formation. Depletion or enrichment of δ18O and δD with depth was not observed and tritium content is also similar at various depths indicating possibility of mixing of groundwater from various depths due to pumping which may lead to contamination of the deeper aquifer by heavy metals and arsenic.  相似文献   

17.
The hydrogeochemical and isotope characteristics of the River Idrijca, Slovenia, where the world’s second largest mercury (Hg) mine is located, were investigated. The River Idrijca, a typical steep mountain river, has an HCO3 −–Ca2+–Mg2+ chemical composition. Its Ca2+/Mg2+ molar ratio indicates that dolomite weathering prevails in the watershed. The River Idrijca and its tributaries are oversaturated with respect to calcite and dolomite. The pCO2 pressure is up to 13 times over atmospheric pressure and represents a source of CO2 to the atmosphere. δ18O values in river water indicate primary control from precipitation and enrichment of the heavy oxygen isotope of infiltrating water recharging the River Idrijca from its slopes. The δ13CDIC values range from −10.8 to −6.6‰ and are controlled by biogeochemical processes in terrestrial environments and in the stream: (1) exchange with atmospheric CO2, (2) degradation of organic matter, (3) dissolution of carbonates, and (4) tributaries. The contributions of these inputs were calculated according to steady state equations and are estimated to be—11%:19%:30%:61% in the autumn and 0%:26%:39%:35% in the spring sampling seasons.  相似文献   

18.
Despite its extreme aridity, the Badain Jaran Desert is rich in groundwater. In the southeastern part of the desert, it is characterized by coexistence of high megadunes and a great number of lakes. Deuterium and oxygen 18 isotope compositions as well as hydrochemistry of groundwater, lake water, soil water and river water were investigated in detail to gain an insight into their relationships and the origin of the ground-water. The results show that the groundwater and the lake water are genetically related, but unrelated to local precipitation and the leakage of Heine River at northern slope of Qilian mountain. δD and δ18O values of deep soil water (lower than 40 cm) and groundwater plot on the same evaporation line E11, which shows that they have the same recharge source. The point of intersection between E11 and LMWL suggests that the groundwater originates from the water resource which has a weighted mean value that is lighter by some 6‰ δ18O than the local precipitation in Badain Jaran Desert. 3H data of water samples shows that the groundwater in Badain Jaran Desert originates from the water recharged after the nuclear test. The deep fault zone underground maybe the water circulation channel based on Helium analysis of groundwater. The result has guiding significance to rational exploitation and utilization of the local groundwater.  相似文献   

19.
Mid-Holocene age fossil-fringing reefs occur along the tectonically stable north coast of Java, Indonesia, presenting an opportunity for sea level and paleoclimate reconstruction. The fossil reef at Point Teluk Awur, near Jepara, Central Java, contains two directly superposed horizons of Porites lobata microatolls. Corals in the lower horizon, 80 cm above modern sea level, yielded Uranium series dates of 7090 ± 90 year BP, while corals in the upper horizon at 1.5 m grew at 6960 ± 60 year BP. These dates match the transgressive phase of regional sea-level curves, but suggest a mid-Holocene highstand somewhat older than that recorded on mid-Pacific islands. Paleotemperature was calibrated using Sr/Ca and δ18O values of a modern P. lobata coral and the locally measured sea surface temperature (SST), yielding SST–Sr/Ca and SST–δ18O calibration equations [T Sr/Ca = 91.03–7.35(Sr/Ca) and Td18 \textO T_{{\delta^{18} {\text{O}}}}  = −3.77 to −5.52(δ18O)]. The application of the local equations to Sr/Ca and δ18O measurements on these corals yielded a range of temperatures of 28.8 ± 1.7°C, comparable to that of the modern Java Sea (28.4 ± 0.7°C). A paleo-salinometer [Δδ18O = ∂δ18O/∂T ( Td18 \textO T_{{\delta^{18} {\text{O}}}}  − T Sr/Ca)], re-calculated using the local parameters, also suggests Java Sea mid-Holocene paleosalinity similar to modern values.  相似文献   

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