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1.
The western Tianshan range is a major Cenozoic orogenic belt in central Asia exposing predominantly Paleozoic rocks including granite. Ongoing deformation is reflected by very rugged topography with peaks over 7000 m high. Active tectonic deformation is tied to an E–W trending fracture and fault system that sections the mountain chain into geologically diverse blocks that extend parallel to the orogen. In the Muzhaerte valley upwelling hot water follows such a fault system in the Muza granite. About 20 L min−1 Na–SO4–Cl water with a temperature of 55 °C having a total mineralization of about 1 g L−1 discharge from the hot spring. The water is used in a local spa that is frequented by the people of the upper Ili river area. Its waters are used for balneological purposes and the spa serves as a therapeutic institution. The major element composition of the hot water is dominated by Na and by SO4 and Cl, Ca is a minor component. Dissolved silica (1.04 mmol L−1) corresponds to a quartz-saturation temperature of 116 °C and a corresponding depth of the source of the water of about 4600 m. This temperature is consistent with Na/K and Na/Li geothermometry. The water is saturated with respect to fluorite and contains 7.5 mg L−1 F− as a consequence of the low Ca-concentration. The water is undersaturated with respect to the primary minerals of the reservoir granite at reservoir temperature causing continued irreversible dissolution of granite. The waters are oversaturated with respect to Ca–zeolite minerals (such as stilbite and mesolite), and it is expected that zeolites precipitate in the fracture pore space and in alteration zones replacing primary granite.  相似文献   

2.
Presented here are halogen concentrations (Cl, Br and I) in pore waters and sediments from three deep cores in gas hydrate fields of the Nankai Trough area. The three cores were drilled between 1999 and 2004 in different geologic regions of the northeastern Nankai Trough hydrate zone. Iodine concentrations in all three cores increase rapidly with depth from seawater concentrations (0.00043 mmol/L) to values of up to 0.45 mmol/L. The chemical form of I was identified as I−, in accordance with the anaerobic conditions in marine sediments below the SO4 reduction depth. The increase in I is accompanied by a parallel, although lesser increase in Br concentrations, while Cl concentrations are close to seawater values throughout most of the profiles. Large concentration fluctuations of the three halogens in pore waters were found close to the lower boundary of the hydrate stability zone, related to processes of formation and dissociation of hydrates in this zone. Generally low concentrations of I and Br in sediments and the lack of correlation between sediment and pore water profiles speak against derivation of I and Br from local sediments and suggest transport of halogen rich fluids into the gas hydrate fields. Differences in the concentration profiles between the three cores indicate that modes of transportation shifted from an essentially vertical pattern in a sedimentary basin location to more horizontal patterns in accretionary ridge settings. Because of the close association between organic material and I and the similarity of transport behavior for I− and CH4, the results suggest that the CH4 in the gas hydrates also was transported by aqueous fluids from older sediments into the present layers.  相似文献   

3.
《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   

4.
Uranium deposits containing molybdenum and fluorite occur in the Central Mining Area, near Marysvale, Utah, and formed in an epithermal vein system that is part of a volcanic/hypabyssal complex. They represent a known, but uncommon, type of deposit; relative to other commonly described volcanic-related uranium deposits, they are young, well-exposed and well-documented. Hydrothermal uranium-bearing quartz and fluorite veins are exposed over a 300 m vertical range in the mines. Molybdenum, as jordisite (amorphous MoS2), together with fluorite and pyrite, increase with depth, and uranium decreases with depth. The veins cut 23-Ma quartz monzonite, 20-Ma granite, and 19-Ma rhyolite ash-flow tuff. The veins formed at 19-18 Ma in a 1 km2 area, above a cupola of a composite, recurrent, magma chamber at least 24 × 5 km across that fed a sequence of 21- to 14-Ma hypabyssal granitic stocks, rhyolite lava flows, ash-flow tuffs, and volcanic domes. Formation of the Central Mining Area began when the intrusion of a rhyolite stock, and related molybdenite-bearing, uranium-rich, glassy rhyolite dikes, lifted the fractured roof above the stock. A breccia pipe formed and relieved magmatic pressures, and as blocks of the fractured roof began to settle back in place, flat-lying, concave-downward, “pull-apart” fractures were formed. Uranium-bearing, quartz and fluorite veins were deposited by a shallow hydrothermal system in the disarticulated carapace. The veins, which filled open spaces along the high-angle fault zones and flat-lying fractures, were deposited within 115 m of the ground surface above the concealed rhyolite stock. Hydrothermal fluids with temperatures near 200 °C, 18OH2O∼−1.5, DH2O∼−130, log f O2 about −47 to −50, and pH about 6 to 7, permeated the fractured rocks; these fluids were rich in fluorine, molybdenum, potassium, and hydrogen sulfide, and contained uranium as fluoride complexes. The hydrothermal fluids reacted with the wallrock resulting in precipitation of uranium minerals. At the deepest exposed levels, wallrocks were altered to sericite; and uraninite, coffinite, jordisite, fluorite, molybdenite, quartz, and pyrite were deposited in the veins. The fluids were progressively oxidized and cooled at higher levels in the system by boiling and degassing; iron-bearing minerals in wall rocks were oxidized to hematite, and quartz, fluorite, minor siderite, and uraninite were deposited in the veins. Near the ground surface, the fluids were acidified by condensation of volatiles and oxidation of hydrogen sulfide in near-surface, steam-heated, ground waters; wall rocks were altered to kaolinite, and quartz, fluorite, and uraninite were deposited in veins. Secondary uranium minerals, hematite, and gypsum formed during supergene alteration later in the Cenozoic when the upper part of the mineralized system was exposed by erosion. Received: 23 June 1997 / Accepted: 15 October 1997  相似文献   

5.
Fluorite can be used as a probe for the source of Sr and REE, as well as for the Sr and Nd isotope systematics of mineralizing solutions, allowing characterization of the composition, oxidation state and sources of the fluids. The 87Sr / 86Sr ratios in vein fluorite from the Santa Catarina Fluorite District, southern Brazil, are low (0.720 to 0.745) relative to those of the majority of host granites at the time of mineralization (90 Ma), but are similar to those of less abundant and less evolved Sr- and Ca-rich granites and plagioclases of the heterogeneous Pedras Grandes granite association. Major contributions of Sr from the unradiogenic Parana Basin rocks (87Sr / 86Sr90 Ma = 0.705 to 0.718) are unlikely, considering the radiogenic character of the lower 87Sr / 86Sr end-member in fluorite mixing lines. Estimated fluorite fluid partition coefficients (KdSr-Ca = 0.019 and DSr ≈ 600) indicate a Sr / Ca ratio in the fluorite-forming solution of 0.012, and Sr contents of 0.05 to 0.25 ppm, which are similar to those of present-day granitic geothermal waters. Initial Nd isotopic compositions of the vein fluorites (0.5120 to 0.512) are similar to those of the Pedras Grandes granites. The 143Nd / 144Nd90 Ma of the evolved granites of the Tabuleiro granite association, their accessory fluorites and the Parana Basin rocks are considerably more radiogenic (0.5120 to 0.5127) and these are thus considered to be unlikely sources of the fluids. The REE patterns of vein fluorites, normalized to upper continental crust, show a range of LREE-depleted patterns, with highly variable positive and negative Eu anomalies. The host Pedras Grandes granites show flat to slightly depleted UCC normalized LREE patterns with strong negative Eu anomalies. Depletion of the LREE in fluorites resulted from the mobility of HREE fluoride complexes during fluid migration. A REE fractionation model based on ionic potential ratios indicates that Eu3+ was stable during fluid migration and fluorite precipitation. The coexistence of pyrite and Eu3+ in the mineralizing fluids is consistent with low pH and oxygen fugacities near the hematite-magnetite buffer.  相似文献   

6.
The authors report here halogen concentrations in pore waters and sediments collected from the Mallik 5L-38 gas hydrate production research well, a permafrost location in the Mackenzie Delta, Northwest Territories, Canada. Iodine and Br are commonly enriched in waters associated with CH4, reflecting the close association between these halogens and source organic materials. Pore waters collected from the Mallik well show I enrichment, by one order of magnitude above that of seawater, particularly in sandy layers below the gas hydrate stability zone (GHSZ). Although Cl and Br concentrations increase with depth similar to the I profile, they remain below seawater values. The increase in I concentrations observed below the GHSZ suggests that I-rich fluids responsible for the accumulation of CH4 in gas hydrates are preferentially transported through the sandy permeable layers below the GHSZ. The Br and I concentrations and I/Br ratios in Mallik are considerably lower than those in marine gas hydrate locations, demonstrating a terrestrial nature for the organic materials responsible for the CH4 at the Mallik site. Halogen systematics in Mallik suggest that they are the result of mixing between seawater, freshwater and an I-rich source fluid. The comparison between I/Br ratios in pore waters and sediments speaks against the origin of the source fluids within the host formations of gas hydrates, a finding compatible with the results from a limited set of 129I/I ratios determined in pore waters, which gives a minimum age of 29 Ma for the source material, i.e. at the lower end of the age range of the host formations. The likely scenario for the gas hydrate formation in Mallik is the derivation of CH4 together with I from the terrestrial source materials in formations other than the host layers through sandy permeable layers into the present gas hydrate zones.  相似文献   

7.
A number of chemical and physical processes inside and outside a sedimentary basin (e.g. evaporite dissolution and topographic drive, respectively) affect groundwater flow near the basin’s margin. Contrasting formations at the margin, typically basinal sedimentary rocks and basement, are host to the interplay between these processes so that groundwater flows and compositions change within a relatively small volume. To interpret how groundwater flow and geochemistry have evolved, interactions between these processes must be understood. Such interactions were investigated near the margin of the East Irish Sea Basin in NW England, by sampling deep groundwaters (to 1500 m below sea level) from Ordovician volcanic basement rocks and Carboniferous to Triassic sedimentary cover rocks. Variable Br/Cl ratios and Cl concentrations in deep saline waters and brines indicate mixing patterns. Variations in 36Cl/Cl constrain the timing of mixing. Relatively low Br/Cl ratios (ca. 1 × 10−3 by mass) characterise brine from the western sedimentary cover and reflect halite dissolution further west. Saline water with relatively high Br/Cl ratios (ca. 2 × 10−3 by mass) of uncertain origin occupies the eastern basement. These two waters mix across the area. However, mixing alone cannot explain variable 36Cl/Cl ratios, which partly reflect differing in situ36Cl production rates in different rock formations. Most 36Cl/Cl ratios in groundwater sampled from the eastern metavolcanic basement (mean = 25 × 10−15) and western sedimentary cover (mean = 10 × 10−15) are at or close to equilibrium with in situ36Cl production. These variations in 36Cl/Cl across the site possibly took >1.5 Ma to be attained, implying that deep groundwater flow responded only slowly to the Quaternary glaciation of the site. Interplay between varied processes in basin marginal settings does not necessarily imply flow instability.  相似文献   

8.
Kinetics of isotopic equilibrium in the mineral radiometric systems of igneous and metamorphic rocks is an important issue in geochronology. It turns out that temperature is the most important factor in dictating isotopic equilibrium or disequilibrium with respect to diffusion mechanism. Contemporaneous occurrence of Mesozoic granites and gneisses in the Dabie orogen of China allows us to evaluate the thermal effect of magma emplacement and associated metamorphism on mineral radiometric systems. Zircon U-Pb, mineral Rb-Sr and O isotope analyses were carried out for a Cretaceous granite and its host gneiss (foliated granite) from North Dabie. Zircon U-Pb dating gave consistently concordant ages of 127 ± 3 Ma and 128 ± 2 Ma for the granite and the gneiss, respectively. A direct correspondence in equilibrium state is observed between the O and Rb-Sr isotope systems of both granitic and gneissic minerals. Mineral O isotope temperatures correlate with O diffusion closure temperatures under conditions of slow cooling, indicating attainment and preservation of O isotope equilibrium in these minerals. The mineral Rb-Sr isochron of granite, constructed by biotite, feldspar, apatite and whole-rock with the O isotope equilibrium, yields a meaningful age of 118 ± 3 Ma, which is in accordance with the mineral Rb-Sr isochron age of 122 ± 1 Ma for the host gneiss. The consistency in both U-Pb and Rb-Sr ages between the granite and the gneiss suggests a contemporaneous process of crystallizing the zircons and resetting the Rb-Sr radiometric systems during magma emplacement and granite foliation. Whereas the zircon U-Pb ages for both granite and gneiss are interpreted as the timing of magma crystallization, the young Rb-Sr isochron ages record the timing of Sr diffusion closure during the slow cooling. Protolith of the gneiss crystallized shortly before intrusion of the granite, so that it was able to be foliated by voluminous emplacement of coeval mafic to felsic magmas derived by anatexis of orogenic lithospheric keel. Therefore, extensional collapse of collision-thickened crust at Early Cretaceous is suggested to trigger the post-collisional magmatism, which in turn serves as an essential driving force for the contemporaneous high-T deformation/metamorphism.  相似文献   

9.
To investigate the possible variations of Rn concentration in crystalline rocks as a function of flow conditions, a field study was carried out of a fractured aquifer in granite. The method is based on the in situ measurement of Rn in groundwater, aquifer tests for the determination of hydraulic characteristics of the aquifer and laboratory measurement of Rn exhalation rate from rocks. A simple crack model that simulates the Rn concentration in waters circulating in a fracture intersecting a borehole was also tested. The Rn concentrations in groundwaters from boreholes of the study site ranged from 192 to 1597 Bq L−1. The Rn exhalation rates of selected samples of granite and micaschist were determined from laboratory experiments. The results yielded fluxes varying from 0.5 to 1.3 mBq m−2 s−1 in granite and from 0.5 to 0.9 mBq m−2 s−1 in micaschists. Pumping tests were performed in the studied boreholes to estimate the transmissivity and calculate the equivalent hydraulic aperture of the fractures. Transmissivities ranged from 10−5 to 10−3 m2 s−1. Using the cubic law, hydraulic equivalent fracture apertures were calculated to be in the range of 0.5–2.3 mm.  相似文献   

10.
The hydrothermal system of Saint-Gervais-les-Bains, France is located in a south western low-elevation point of the Aiguilles Rouges crystalline Massif. The crystalline rocks are not directly outcropping in the studied area but certainly exist beyond 300 m depth. Uprising waters are pumped from two different aquifers below the Quaternary deposits of the Bon Nant Valley. In the Lower Trias-Permian aquifer crossed by De Mey boreholes (27–36 °C), the ascending Na-SO4 and high-Cl thermal water from the basement (4.8 g/L) is mostly mixed by a Ca-SO4 and low-Cl cold water circulating in the autochthonous cover of the Aiguilles Rouges Basement. The origin of the saline thermal water probably results from infiltration and circulation in the basement until it reaches deep thrust faults with leaching of residual brines or fluid inclusions at depth (Cl/Br molar ratio lower than 655). The dissolution of Triassic halite (Cl/Br > 1000) is not possible at Saint-Gervais-les-Bains because the Triassic cold waters have a low-Cl concentration (< 20 mg/L). Water–rock interactions occur during the upflow via north–south strike-slip faults in the basement and later on in the autochthonous cover. For the De Mey Est borehole, gypsum dissolution is occurring with cationic exchanges involving Na, as well as low-temperature Mg dissolution from dolomite in the Triassic formations. The aquifer of imbricated structures (Upper-Middle Trias) crossed by the Lépinay well (39 °C) contains thermal waters, which are strongly mixed with a low-Cl water, where gypsum dissolution also occurs. The infiltration area for the thermal end-member is in the range 1700–2100 m, close to the Lavey-les-Bains hydrothermal system corresponding to the Aiguilles Rouges Massif. For the Ca-SO4 and low-Cl end-member, the infiltration area is lower (1100–1300 m) showing circulation from the Mont Joly Massif. The geothermometry method indicates a reservoir temperature of probably up to 65 °C but not exceeding 100 °C.  相似文献   

11.
The chemical composition of water sampled in a 700 m deep underground barite-fluorite mine in the crystalline basement of the Black Forest area (SW Germany) varies systematically with depth and the length of flow paths trough, the fracture porosity of the gneiss matrix. Calcium and sulfate increase as a result of a combined sulfide oxidation and plagioclase alteration reaction. The gneiss contains andesine–plagioclase (An20–An40) and is rich in primary sulfide. As an effect of Ca and SO4 release by the prime water–rock reaction, dissolved oxygen decreases and the waters become more reduced. The waters have Cl/Br mass ratios of about 50, which is very close to that of experimentally leached gneiss powders indicating that the rock matrix is the source of the halogens. The waters are undersaturated with respect to calcite in the upper parts of the mine. With increasing reaction progress, calcite saturation is reached and carbonate forms as a reaction product of the prime reaction that also controls the partial pressure of CO2 to progressively lower values. The chemical evolution of groundwater in fractured basement of the Clara mine suggests that the partial pressure of CO2 is an internally buffered parameter rather than a controlling external variable.  相似文献   

12.
Origin of salinity of deep groundwater in crystalline rocks   总被引：2，自引：0，他引：2  
Stober  & Bucher 《地学学报》1999,11(4):181-185
Deep groundwater in fractured crystalline basement has been reported from deep mines and from scientific deep wells. Highly saline brines have been described from several km depth in the continental basement of the Canadian, Fennoscandian and Ukrainian shields and elsewhere in the world. The origin of salinity is unknown and many different possibilities have been presented. We compare the compositional evolution of deep waters in the Black Forest basement, SW Germany, with those of other deep crystalline waters, and use halogen systematics (e.g. Cl/Br ratios) and other parameters of the waters to deduce the origin of their salinity. In the Black Forest the composition of deep thermal waters results from chemical interaction of surface water with the rock matrix (mainly weathering of plagioclase and mica) and from mixing of the reacted water with stagnant saline deep water. Here we show by Na/TDS-and Cl/TDS-investigations, by molality-ratios of the Na and Cl concentrations, and by Cl/Br systematics that these deep saline waters have a marine origin. The Cl/Br ratios in deep crystalline waters are very close to normal marine ratios (Cl/Br = 288 ppm basis). In contrast, Cl/Br ratios of other possible sources of salinity show distinctly different Cl/Br ratios: water derived from dissolved Tertiary halite deposits of the rift valley is in the order of Cl/Br = 2400 and water from dissolved Muschelkalk halite deposits has values of about Cl/Br = 9900. Leaching experiments on crystalline rocks, on the other hand, show that the average Cl/Br ratio of crystalline rocks is far below Cl/Br = 100.  相似文献   

13.
A mathematical model is presented that describes the effects of pore fluid aqueous diffusion and reaction rate on the isotopic exchange between fluids and rocks in reactive geo-hydrological systems where flow is primarily through fractures. The model describes a simple system with parallel equidistant fractures, and chemical transport in the matrix slabs between fractures by aqueous diffusion through a stagnant pore fluid. The solid matrix exchanges isotopes with pore fluid by solution-precipitation at a rate characterized by a time constant, R (yr−1), which is an adjustable parameter. The effects of reaction on the isotopes of a particular element in the fracture fluid are shown to depend on the ratio of the diffusive reaction length for that element (L) to the fracture spacing (b). The reaction length depends on the solid-fluid exchange rate within the matrix, the partitioning of the element between the matrix pore fluid and the matrix solid phase, the porosity and density of the matrix, and the aqueous diffusivity. For L/b < 0.3, fluid-rock isotopic exchange is effectively reduced by a factor of 2L/b relative to a standard porous flow (single porosity) model. For L/b > 1, the parallel fracture model is no different from a porous flow model. If isotopic data are available for two or more elements with different L values, it may be possible to use the model with appropriate isotopic measurements to estimate the spacing of the primary fluid-carrying fractures in natural fluid-rock systems. Examples are given using Sr and O isotopic data from mid-ocean ridge (MOR) hydrothermal vent fluids and Sr isotopes in groundwater aquifers hosted by fractured basalt. The available data for MOR systems are consistent with average fracture spacing of 1-4 m. The groundwater data suggest larger effective fracture spacing, in the range 50-500 m. In general, for fractured rock systems, the effects of fracture-matrix diffusive exchange must be considered when comparing isotopic exchange effects for different elements, as well as for estimating water age using radioactive and cosmogenic isotopes.  相似文献   

14.
The largest gold district in China is the Jiaodong Peninsula, where three types of gold deposits are recognized: quartz vein, fracture-altered and breccia types. The first two developed along a group of NE-trending faults and are hosted by granitic intrusions, dated at 160 to 150 Ma (biotite granite) and 130 to 126 Ma (granodiorite), and by metamorphic rocks of the Precambrian crystalline basement. The breccia-type gold system is mainly located around the northern margin of the Jiaolai Cretaceous basin, where mineralisation is controlled by both detachment fractures and NE-trending faults. This study is based on stable isotope determinations from ten gold deposits, including Linglong, Jiaojia, Sanshandao, Cangshang, Wang'ershan, Dayigezhuang, Denggezhuang, Pengjiakuang, Fayunkuang and Dazhuangzi, as well as the Linglong Jurassic biotite granite, Guojialing Cretaceous granodiorite and Archean gneiss. The stable isotope systematics reflect the style of the three types of gold deposits, but also show that they belong to the same metallogenic system, in which the hydrothermal fluids were derived from a mantle fluid reservoir and mixed with crustal fluids. The ore-forming age is later than both the Jurassic biotite granite and Cretaceous granodiotite, but overlaps with the 121 to 114 Ma ages of lamprophyre and diabase dykes. The hydrothermal fluids that were responsible for both gold mineralisation and the retrograde alteration of the diabase and lamprophyre dykes are similar, and represent a CO2 and potassium-rich system. This fluid system is interpreted to be the consequence of Cretaceous lithospheric thinning, asthenospheric upwelling and mantle degassing in Eastern China.  相似文献   

15.
为了解阿尔金山前带东段基岩储层主要特征,对储层进行评价.在野外露头踏勘、岩心观察描述、薄片鉴定及相关分析测试的基础上,结合普通测井资料、成像测井资料及孔渗密实验数据等进行分析.结果表明,阿尔金山前带东段基岩储层岩性主要是岩浆岩和变质岩,岩浆岩以花岗岩为主,变质岩以片麻岩为主.储集空间类型主要包括未完全充填裂缝、溶蚀孔洞和基质微孔3类.基岩储层孔隙度介于0.004%~9.760%,平均孔隙度在1.663%~3.844%;渗透率介于最大值0.002~33.239mD,平均渗透率在0.020~3.836 mD,片麻岩类物性整体好于花岗岩类,孔隙度和渗透率之间没有明显的相关性.基岩储层主控因素包括岩性及矿物组合、古地貌、先存断裂及破碎带、后期岩浆侵入及热液作用4个方面.结合基岩储层的物性特征及形成的主控因素,建立了多因素控制的基岩储层评价标准,将储层分为好、中等、较差、差4类.评价结果表明,研究区多以Ⅱ类储层为主,主要见于花岗片麻岩,其次是花岗岩、黑云母斜长片麻岩等.东坪鼻隆、牛中-牛北斜坡可见Ⅰ类储层;尖北斜坡、牛东鼻隆、冷北斜坡多为Ⅱ类储层.   相似文献   

16.
Analyses of halogen concentration and stable chlorine isotope composition of fluid inclusions from hydrothermal quartz and carbonate veins spatially and temporally associated with giant unconformity-related uranium deposits from the Paleoproterozoic Athabasca Basin (Canada) were performed in order to determine the origin of chloride in the ore-forming brines. Microthermometric analyses show that samples contain variable amounts of a NaCl-rich brine (Cl concentration between 120,000 and 180,000 ppm) and a CaCl2-rich brine (Cl concentration between 160,000 and 220,000 ppm). Molar Cl/Br ratios of fluid inclusion leachates range from ∼100 to ∼900, with most values between 150 and 350. Cl/Br ratios below 650 (seawater value) indicate that the high salinities were acquired by evaporation of seawater. Most δ37Cl values are between −0.6‰ and 0‰ (seawater value) which is also compatible with a common evaporated seawater origin for both NaCl- and CaCl2-rich brines.Slight discrepancies between the Cl concentration, Cl/Br, δ37Cl data and seawater evaporation trends, indicate that the evaporated seawater underwent secondary minor modification of its composition by: (i) mixing with a minor amount of halite-dissolution brine or re-equilibration with halite during burial; (ii) dilution in a maximum of 30% of connate and/or formation waters during its migration towards the base of the Athabasca sandstones; (iii) leaching of chloride from biotites within basement rocks and (iv) water loss by hydration reactions in alteration haloes linked to uranium deposition.The chloride in uranium ore-forming brines of the Athabasca Basin has an unambiguous dominantly marine origin and has required large-scale seawater evaporation and evaporite deposition. Although the direct evidence for evaporative environments in the Athabasca Basin are lacking due to the erosion of ∼80% of the sedimentary pile, Cl/Br ratios and δ37Cl values of brines have behaved conservatively at the basin scale and throughout basin history.  相似文献   

17.
The origin and evolution of formation water from Upper Jurassic to Upper Cretaceous mudstone–packstone–dolomite host rocks at the Jujo–Tecominoacán oil reservoir, located onshore in SE-Mexico at a depth from 5200 to 6200 m.b.s.l., have been investigated, using detailed water geochemistry from 12 producer wells and six closed wells, and related host rock mineralogy. Saline waters of Cl–Na type with total dissolved solids from 10 to 23 g/L are chemically distinct from hypersaline Cl–Ca–Na and Cl–Na–Ca type waters with TDS between 181 and 385 g/L. Bromine/Cl and Br/Na ratios suggest the subaerial evaporation of seawater beyond halite precipitation to explain the extreme hypersaline components, while less saline samples were formed by mixing of high salinity end members with surface-derived, low salinity water components. The dissolution of evaporites from adjacent salt domes has little impact on present formation water composition. Geochemical simulations with Harvie-Mφller-Weare and PHRQPITZ thermodynamic data sets suggest secondary fluid enrichment in Ca, HCO3 and Sr by water–rock interaction. The volumetric mass balance between Ca enrichment and Mg depletion confirms dolomitization as the major alteration process. Potassium/Cl ratios below evaporation trajectory are attributed to minor precipitation of K feldspar and illitization without evidence for albitization at the Jujo–Tecominoacán reservoir. The abundance of secondary dolomite, illite and pyrite in drilling cores from reservoir host rock reconfirms the observed water–rock exchange processes. Sulfate concentrations are controlled by anhydrite solubility as indicated by positive SI-values, although anhydrite deposition is limited throughout the lithological reservoir column. The chemical variety of produced water at the Jujo–Tecominoacán oil field is related to a sequence of primary and secondary processes, including infiltration of evaporated seawater and original meteoric fluids, the subsequent mixing of different water types and the formation of secondary minerals by water–rock interaction. A best fit between measured and calculated reservoir temperatures was obtained with the Mg–Li geothermometer for high salinity formation water (TDS > 180 g/L), whereas Na–K, Na–Ka–Ca and quartz geothermometers are partially applicable for less salinite water (TDS < 23 g/L).  相似文献   

18.
Saline groundwaters were recovered from undisturbed (Restigouche deposit) and active (Brunswick #12 mine) Zn-Pb volcanogenic massive sulfide deposits in the Bathurst Mining Camp (BMC), northern New Brunswick, Canada. These groundwaters, along with fresh to brackish meteoric ground and surface waters from the BMC, have been analyzed to determine their major, trace element and stable isotopic (O, H, C, and B) compositions. Saline groundwaters (total dissolved solids = 22-45 g/L) are characterized by relatively high Na/Ca ratios compared to brines from the Canadian Shield and low Na/Clmolar and δ11B isotopic compositions (−2.5‰ to 11.1‰) compared to seawater. Although saline waters from the Canadian Shield commonly have oxygen and hydrogen isotopic compositions that plot to the left of the global meteoric water line, those from the BMC fall close to the water line. Fracture and vein carbonate minerals at the Restigouche deposit have restricted carbon isotopic compositions of around −5‰ to −6‰. The carbon isotopic compositions of the saline waters at the Restigouche deposit (+12‰ δ13CDIC) are the result of fractionation of dissolved inorganic carbon by methanogenesis. We suggest that, unlike previous models for shield brines, the composition of saline waters in the BMC is best explained by prolonged water-rock reaction, with no requirement of precursor seawater. We suggest that elevated Br/Cl ratios of saline waters compared to seawater may be explained by differential uptake of Br and Cl during groundwater evolution through water-rock reaction.  相似文献   

19.
The oxidation of sulfide-rich rocks, mostly leftover debris from Cu mining in the early 20th century, is contributing to metal contamination of local coastal environments in Prince William Sound, Alaska. Analyses of sulfide, water, sediment, precipitate and biological samples from the Beatson, Ellamar, and Threeman mine sites show that acidic surface waters generated from sulfide weathering are pathways for redistribution of environmentally important elements into and beyond the intertidal zone at each site. Volcanogenic massive sulfide deposits composed of pyrrhotite and (or) pyrite + chalcopyrite + sphalerite with subordinate galena, arsenopyrite, and cobaltite represent potent sources of Cu, Zn, Pb, As, Co, Cd, and Hg. The resistance to oxidation among the major sulfides increases in the order pyrrhotite ? sphalerite < chalcopyrite ? pyrite; thus, pyrrhotite-rich rocks are typically more oxidized than those dominated by pyrite. The pervasive alteration of pyrrhotite begins with rim replacement by marcasite followed by replacement of the core by sulfur, Fe sulfate, and Fe–Al sulfate. The oxi dation of chalcopyrite and pyrite involves an encroachment by colloform Fe oxyhydroxides at grain margins and along crosscutting cracks that gradually consumes the entire grain. The complete oxidation of sulfide-rich samples results in a porous aggregate of goethite, lepidocrocite and amorphous Fe-oxyhydroxide enclosing hydrothermal and sedimentary silicates. An inverse correlation between pH and metal concentrations is evident in water data from all three sites. Among all waters sampled, pore waters from Ellamar beach gravels have the lowest pH (∼3) and highest concentrations of base metals (to ∼25,000 μg/L), which result from oxidation of abundant sulfide-rich debris in the sediment. High levels of dissolved Hg (to 4100 ng/L) in the pore waters probably result from oxidation of sphalerite-rich rocks. The low-pH and high concentrations of dissolved Fe, Al, and SO4 are conducive to precipitation of interstitial jarosite in the intertidal gravels. Although pore waters from the intertidal zone at the Threeman mine site have circumneutral pH values, small amounts of dissolved Fe2+ in the pore waters are oxidized during mixing with seawater, resulting in precipitation of Fe-oxyhydroxide flocs along the beach–seawater interface. At the Beatson site, surface waters funneled through the underground mine workings and discharged across the waste dumps have near-neutral pH (6.7–7.3) and a relatively small base-metal load; however, these streams probably play a role in the physical transport of metalliferous particulates into intertidal and offshore areas during storm events. Somewhat more acidic fluids, to pH 5.3, occur in stagnant seeps and small streams emerging from the Beatson waste dumps. Amorphous Fe precipitates in stagnant waters at Beatson have high Cu (5.2 wt%) and Zn (2.3 wt%) concentrations that probably reflect adsorption onto the extremely high surface area of colloidal particles. Conversely, crystalline precipitates composed of ferrihydrite and schwertmannite that formed in the active flow of small streams have lower metal contents, which are attributed to their smaller surface area and, therefore, fewer reactive sorption sites. Seeps containing precipitates with high metal contents may contribute contaminants to the marine environment during storm-induced periods of high runoff. Preliminary chemical data for mussels (Mytilus edulis) collected from Beatson, Ellamar, and Threeman indicate that bioaccumulation of base metals is occurring in the marine environment at all three sites.  相似文献   

20.
Primary multiphase brine fluid inclusions in omphacite and garnet from low‐ to medium‐temperature eclogites have been analysed for Cl, Br, I, F, Li and SO4. Halogen contents and ratios provide information about trapped lower crustal fluids, even though the major element (Na, K, Ca) contents of inclusion fluids have been modified by fluid–mineral interactions and (step‐) daughter‐crystal formation after trapping. Halogens in the inclusion fluids were analysed with crush–leach techniques. Cl/Br and Cl/I mass ratios of eclogite fluids are in the range 31–395 and 5000–33 000, respectively. Most fluids have a Cl/Br ratio lower than modern seawater and a Cl/I ratio one order of magnitude lower than modern seawater. Fluids with the lowest Cl/Br and highest Cl/I ratios come from an eclogite that formed by hydration of granulite facies rocks, and may indicate that Br and I are fractionated into hydrous minerals. Reconstructions indicate that the inclusion fluids originally contained 500–4000 ppm Br, 1–14 ppm I and 33–438 ppm Li. Electron microprobe analyses of eclogite facies amphibole, biotite, phengite and apatite indicate that F and Cl fractionate most strongly between phengite (F/Cl mass ratio of 1469 ± 1048) and fluid (F/Cl mass ratio of 0.008), and the least between amphibole and fluid. The chemical evolution of Cl and Br in pore fluids during hydration reactions is in many ways analogous to Cl and Br in seawater during evaporation: the Cl/Br ratio remains constant until the aH2O value is sufficiently lowered for Cl to be removed from solution by incorporation into hydrous minerals.  相似文献   

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