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1.
《Chemical Geology》2003,193(3-4):273-293
The El Berrocal granite/U-bearing quartz vein (UQV) system has been studied as a natural analogue of a high-level radioactive waste repository. The main objective was to understand the geochemical behaviour of natural nuclides under different physicochemical conditions. Within this framework, the argillization processes related to fracturing and formation of the uranium–quartz vein were studied from a mineralogical and isotopic standpoint in order to establish their temperatures of formation and thus complete the geothermal history of the system. For this purpose, δ18O values were determined for pure mineral from the unaltered granite and quartz from the uranium–quartz vein, as well as for mixture samples from the hydrothermally altered granite (sericitised granite) and clayey samples from fracture fillings, including the clayey walls of the uranium–quartz vein. The isotopic signature of quartz from the uranium–quartz vein and the monophasic nature of its fluid inclusions led us to conclude that the isotopic signature of water in equilibrium with quartz was approximately in the range from −8.3‰ to −5.7‰ V-SMOV, its temperature of formation being around 85–120 °C. The δ18O values of pure sericite from the hydrothermally altered granite, calculated by means of the oxygen fraction molar method, indicate that its temperature of formation, in equilibrium with the aforementioned waters, is also in the range from 70 °C to approximately 120 °C. Clays from fracture fillings and clayey walls of the uranium–quartz vein are usually mixtures, in different proportions, of illite, approximately formed between 70 and 125 °C; two generations of kaolinite formed at approximately 90–130 °C and at around 25 °C, respectively; smectite, formed at ≤25 °C; and occasionally palygorskite, formed either between 30 and 45 °C or 19 and 32 °C, depending on the fractionation equation used. These data suggest that sericite from the hydrothermally altered granite, quartz from the uranium–quartz vein, illite and the first generation of kaolinite from the fracture fillings resulted from the same hydrothermal process affecting the El Berrocal granite in relation to fracturing. Under certain physicochemical conditions (T≈100 °C, pH≈8 and log [H4SiO4] between −4 and −3), illite and kaolinite can be paragenetic. As a result of weathering processes, smectite was formed from hydrothermal illite and inherited albite under alkaline weathering, while the second generation of kaolinite was formed from smectite, under acid conditions and close to the sulphide-rich uranium–quartz vein. Palygorskite is an occasional mineral formed probably either during the thermal tail of the above-described hydrothermal process or during weathering processes. In both cases, palygorskite must have formed from alkaline Si–Mg-rich solutions. Finally, these data and processes are discussed in terms of natural analogue processes, drawing some implications for the performance assessment of a deep geological radwaste repository (DGRR). 相似文献
2.
Carbonate concretions, lenses and bands in the Pleistocene, Palaeogene and Upper Triassic coalfields of Japan consist of various carbonate minerals with varied chemical compositions. Authigenic carbonates in freshwater sediments are siderite > calcite > ankerite > dolomite >> ferroan magnesite; in brackish water to marine sediments in the coal measures, calcite > dolomite > ankerite > siderite >> ferroan magnesite; and in the overlying marine deposits, calcite > dolomite >> siderite. Most carbonates were formed progressively during burial within a range of depths between the sediment-water interface and approximately 3 km. The mineral species and the chemical composition of the carbonates are controlled primarily by the initial sedimentary facies of the host sediments and secondarily by the diagenetic evolution of pore water during burial. Based on the regular sequence and burial depth of precipitation of authigenic carbonates in a specific sedimentary facies, three diagenetic stages of carbonates are proposed. Carbonates formed during Stage I (< 500 m) strongly reflect the initial sedimentary facies, e.g. low Ca-Mg siderite in freshwater sediments which are initially rich in iron derived from lateritic soil on the nearby landmass, and Mg calcite and dolomite in brackish-marine sediments whose pore waters abound in Ca2+ and Mg2+ originating in seawater and calcareous shells. Carbonates formed during Stage II (500–2000 m) include high Ca-Mg siderite, ankerite, Fe dolomite and Fe–Mg calcite in freshwater sediments. The assemblage of Stage II carbonates in brackish-marine sediments in the coal measures is similar to that in freshwater sediments. This suggests similar diagenetic environments owing to an effective migration and mixing of pore water due to the compaction of host sediments. Carbonates formed during Stage III (> 2000 m) are Fe calcite and extremely high Ca-Mg siderite; the latter is exclusively in marine mudstones. The supply of Ca is partly from the alteration of silicates in the sediments at elevated burial temperatures. After uplift, calcite with low Mg content precipitates from percolating groundwater and fills extensional cracks. 相似文献
3.
Kenneth M. Voglesonger John R. Holloway Eileen E. Dunn Peter J. Dalla-Betta Peggy A. O''Day 《Chemical Geology》2001,180(1-4):129-139
The abiotic synthesis of organic compounds in seafloor hydrothermal systems is one mechanism through which the subsurface environment could be supplied with reduced carbon. A flow-through, fixed-bed laboratory reactor vessel, the Catalytic Reactor Vessel (CRV) system, has been developed to investigate mineral–surface promoted organic synthesis at temperatures up to 400°C and pressures up to 30 MPa, conditions relevant to seafloor hydrothermal systems. Here we present evidence that metastable methanol can be directly synthesized from a gas-rich CO2–H2–H2O mixture in the presence of a mineral substrate. Experiments have been performed without a substrate, with quartz, and with a mixture of quartz and magnetite. Temperatures and pressures in the experiments ranged from 200°C to 350°C and from 15 to 18 MPa, respectively. Maximum conversion of 5.8×10−4% CO2 to CH3OH per hour was measured using a mixture of magnetite and quartz in the reactor. After passivation of the stainless steel reactor vessel, experiments demonstrate that methanol is formed at temperatures up to 350°C in the presence of magnetite, and that the formation rate decreases over time. The experiments also show a loss of surface reactivity at 310°C and a regeneration of surface reactivity with increased temperature up to 350°C. Concentrations of CO2 and H2 used in the experiments simulate periodic, localized and dynamic conditions occurring within the seafloor during and immediately following magmatic diking events. High concentrations of CO2 and H2 may be generated by dike injection accompanied by exsolution of CO2 and reaction of dissolved H2O with FeO in the magma to form H2. The experiments described here examine how the ephemeral formation of an H2–CO2-rich vapor phase within seafloor hydrothermal systems may supply reactants for abiotic organic synthesis reactions. These experiments show that the presence of specific minerals can promote the abiotic synthesis of simple organic molecules from common inorganic reactants such H2O, CO2 and H2 under geologically realistic conditions. 相似文献
4.
Anja M. Schleicher Laurence N. Warr Bernd Kober Emmanuel Laverret Norbert Clauer 《Contributions to Mineralogy and Petrology》2006,152(3):349-364
Episodic and localized illite mineralization is documented in the hydrothermally altered Soultz-sous-Forêts granite (Upper Rhine Graben, France). Separated grain-size fractions of altered granite and argillite vein samples contain mixtures of 2M1 and 1M trans-vacant illite varieties. The platy pseudohexagonal 2M1 illite phases dominate the vein fillings, whereas the 1M illite occurs largely as a fibrous pore-filling variety, which is particularly abundant in the granite matrix. Multiple phases of fluid injections into the granite body have resulted in different illite assemblages, each sample containing a mixture of polytype generations formed during different crystal growth events. On the basis of mineralogical and K–Ar isotopic constraints, the ages of these vein-mineralizing events are determined by plotting the K–Ar values of the various grain-size fractions against polytype abundance and the fitted volume-weighted crystallite thickness distributions. The results suggest a Permian age for the formation of the studied argillite veins, characterized by successive injections of hydrothermal fluids. Secondary episodes of illite crystallization occurred during Jurassic and Cretaceous (or even younger times) in both the veins and the granite matrix. There are indications that the polytype structure and composition of illite were strongly influenced by variations in fluid chemistry and the degree of fluid–rock interaction as the granite was progressively sealed during post-Variscan, episodic hydrothermal activity. 相似文献
5.
J. G. Liou 《Lithos》1971,4(4):389-402
The stability fields of analcime and analcime+quartz have been investigated using conventional hydrothermal techniques, over the approximate range of conditions 160–600 °C and 500–5000 bars fluid pressure. The dehydration of analcime (Na2Al2Si3·3O11·6 · nH2O) to albite, nepheline and H2O occurs at temperatures of 492±5 °C at 500 bars, 538±5 °C at 1000 bars, 578±5 °C at 2000 bars and 598±5 °C at 3000 bars. In the presence of quartz, analcine dehydrates to highly disordered albite and H2O at about 200 °C and 2000 bars, 196°±5 °C and 3000 bars, about 190 °C and 4000 bars, and 183±5 °C at 5000 bars Pfluid. The synthetic phase equilibria appear to be compatible with field observations that primary analcimes occur as phenocrysts or in groundmass in some volcanic and hypabyssal rocks and secondary analcimes in sedimentary, hydrothermally altered and low-grade metamorphic rocks. 相似文献
6.
Subías I. Yuste A. Fanlo I. Fernández-Nieto C. González López J.M. 《Geologie en Mijnbouw》1999,78(1):87-102
Mineralogical, textural and geochemical investigations were made to determine the post-depositional evolution of Devonian and Early Carboniferous carbonates from Valle de Tena. The carbonate association is made up of low-Mg calcite, which occurs as micrite, spar cements, neomorphic patches and spar filling veinlets. Non-stoichiometric dolomite and ankerite occur as cements (dolomite also as replacements) in the Middle Devonian, post-dating calcite types. All these phases pre-date tectonic stylolites, indicating compaction after stabilization of the carbonate minerals. Strontium concentrations indicate that Early Devonian and Early Carboniferous micrites initially precipitated as aragonite; Middle and Late Devonian micrites precipitated as high-Mg calcites. Both precursors were diagenetically stabilized to low-Mg calcites through interaction with meteoric waters in phreatic environments. Trace elements in dolomite and ankerite indicate precipitation from Sr-enriched meteoric water. All studied carbonates, except Middle Devonian limestones, precipitated in reducing environments, which favoured incorporation of Fe and Mn. Late calcite generations precipitated from more saline waters than micrites. Light 18O values in micrites suggest alteration mainly in meteoric-phreatic environments. The dolomites and ankerites precipitated from more 18O-depleted fluids than the calcites, suggesting a greater contribution from meteoric waters. Variations in 13C of micrites represent primary secular trends, according to published 13C variations. The 13C oscillations within each succession probably relate to sea-level oscillations. Strontium isotopes also point to a meteoric origin of diagenetic fluids. Model calculations suggest that O and Sr isotopes equilibrated between calcites and fluid at relatively low water/rock ratios, whereas C isotopic signatures are inherited from limestones. 相似文献
7.
利用岩芯和薄片资料,通过薄片孔隙描述、铸体薄片图像分析等方法,在对研究区马五41储层孔隙类型划分的基础上,详细划分了膏模孔充填类型,并对其充填过程进行了阐述。研究结果表明,研究区马五41储层主要发育溶蚀孔（膏模孔和其他溶孔）、晶间孔、晶间溶孔、微裂缝4种类型的孔隙,且以膏模孔为主。通过镜下薄片对膏模孔内不同充填物观察发现,充填物主要为白云石、方解石、硬石膏,其中半充填的膏模孔中主要充填物为白云岩粉砂、白云岩粉砂+石英、白云岩粉砂+铁白云石3种类型,而全充填的膏模孔中主要充填物为白云岩粉砂+方解石、白云岩粉砂+石英+方解石、白云岩粉砂+硬石膏3种类型。综合分析认为膏模孔是含膏云岩中石膏等易溶晶体溶蚀后,晶体轮廓保留而形成的,首先裸露风化壳期先充填白云岩粉砂和深灰色方解石,其次深埋藏期充填自生石英、白色亮晶方解石、铁白云石及硬石膏。 相似文献
8.
Fluid inclusion studies combined with the isotope geochemistry of several generations of fracture calcite from the Olkiluoto research site, Finland, has been used to better understand the past thermal and fluid history in the crystalline rock environment. Typically, fracture mineral investigations use O and C isotopes from calcite and an estimate of the isotopic composition of the water that precipitated the calcite to perform δ18O geothermometry calculations to estimate past temperature conditions. By combining fluid inclusion information with calcite isotopes, one can directly measure the temperature at which the calcite formed and can better determine past fluid compositions. Isotopic, petrologic and fluid inclusion studies at the Olkiluoto research site in Finland were undertaken as part of an investigation within the Finnish nuclear waste disposal program. The study revealed that four fluids were recorded by fracture calcites. From petrologic evidence, the first fluid precipitated crystalline calcite at 151–225°C with a δ13C signature of −21 to −13.9‰ PDB and a δ18O signature of 12.3–13.0‰ SMOW. These closed fracture fillings were found at depths greater than 500 m and were formed from a high temperature, low salinity, Na–Cl fluid of possible meteoric water altered by exchange with wallrock or dilute basinal origin. The next fluid precipitated crystalline calcite with clay at 92–210°C with a δ13C signature of −2.6 to +3.8‰ PDB and a δ18O signature of 19.4–20.7‰ SMOW. These closed fracture fillings were found at depths less than 500 m and were formed from a moderate to high temperature, low to moderate salinity, Na–Cl fluid, likely of magmatic origin. The last group of calcites to form, record the presence of two distinct fluid types. The platy (a) calcite formed at 95–238°C with a δ13C signature of −12.2 to −3.8‰ PDB and a δ18O signature of 14.9–19.6‰ SMOW, from a high temperature, low salinity, Na–Cl fluid of possible magmatic origin. The platy (b) calcite formed at 67–98°C with a δ13C signature of −13.0 to −6.2‰ PDB and a δ18O signature of 15.1–20.1‰ SMOW, from a low temperature, high salinity, Ca–Na–Cl fluid of possible basinal brine origin. The two calcites are related through a mixing between the two end members. The source of the fluids for the platy grey (a) calcites could be the olivine diabase dykes and sills that cut through the site. The source of fluids for the platy (b) calcites could be the Jotnian arkosic sandstone formations in the northern part of the site. At the Olkiluoto site, δ18O geothermometry does not agree with fluid inclusion data. The original source of the water that forms the calcite has the largest effect on the isotopic signature of the calcites formed. Large isotopic shifts are seen in any water by mineral precipitation during cooling under rock–water equilibrium fractionation conditions. Different calcite isotopic signatures are produced depending on whether cooling occurred in an open or closed system. Water–rock interaction, at varying W/R ratios, between a water and a host rock can explain the isotopic shifts in many of the calcites observed. In some cases it is possible to shift the δ18O of the water by +11.5‰ (SMOW) using a realistic water–rock ratio. This process still does not explain some of the very positive δ18O values calculated using fluid inclusion data. Several other processes, such as low temperature recrystallization, boiling, kinetic effects and dissolution of calcite from fluid inclusion walls can affect isotopic signatures to varying degrees. The discrepancy between fluid inclusion data and δ18O geothermometry at the Olkiluoto site was most likely due to poor constraint on the original source of the water. 相似文献
9.
Hydrothermal mixing,carbonate dissolution and sulfide precipitation in Mississippi Valley-type deposits 总被引：1，自引：0，他引：1
A large number of Mississippi Valley-Type (MVT) deposits are located within dissolution zones in carbonate host rocks. Some genetic models propose the existence of cavities generated by an earlier event such as a shallow karstification, that were subsequently filled with hydrothermal minerals. Alternative models propose carbonate dissolution caused by the simultaneous precipitation of sulfides. These models fail to explain either the deep geological setting of the cavities, or the observational features which suggest that the dissolution of carbonates and the precipitation of minerals filling the cavities are not strictly coeval. We present a genetic model inspired by the textural characteristics of MVT deposits that accounts for both the dissolution of carbonate and precipitation of sulfides and later carbonates in variable volumes. The model is based on the mixing of two hydrothermal fluids with a different chemistry. Depending on the proportion of the end members, the mixture dissolves and precipitates carbonates even though the two mixing solutions are both independently saturated in carbonates. We perform reactive transport simulations of mixing of a regional groundwater and brine ascending through a fracture, both saturated in calcite, but with different overall chemistries (Ca and carbonate concentrations, pH, etc). As a result of the intrinsic effects of chemical mixing, a carbonate dissolution zone, which is enhanced by acid brines, appears above the fracture, and another zone of calcite precipitation builds up between the cavity and the surrounding rock. Sulfide forms near the fracture and occupies a volume smaller than the cavity. A decline of the fluid flux in the fracture would cause the precipitation of calcite within the previously formed cavities. Therefore, dissolution of carbonate host rock, sulfide precipitation within the forming cavity, and later filling by carbonates may be part of the same overall process of mixing of fluids in the carbonate host rock.Editorial handling: C. Everett 相似文献
10.
The differentiated Mesozoic alkali dolerite Prospect Intrusion contains a wide range of secondary minerals, including carbonates (primarily calcite), laumontite, prehnite and heulandite, whose stability relationships imply a formation temperature of <200°C. The δ18O data for carbonates define a higher temperature (160 – 195°C) suite, and a lower temperature (51 – 73°C) suite. The δ13C, δ18O and 87Sr/86Sr isotope systematics for these carbonates suggest derivation of the higher temperature group from magmatic fluids, whereas the other group had a major meteoric component that probably originated from porewater in the country rock. Source fluids for prehnite were meteoric rather than magmatic in origin based on their δD and δ18O ratios. Early in the intrusion's emplacement, CO2-rich hydrothermal fluids formed a carbonate rind sealing the upper part of the hydrothermal system and produced the higher temperature carbonates (calcite) and laumontite. Later, cooler fluids with a meteoric component infiltrated vesicles and fractures, depositing the lower temperature carbonates (calcite, aragonite), heulandite and prehnite. 相似文献
11.
Kentaro Nakamura 《Geochimica et cosmochimica acta》2004,68(22):4595-4618
Early Archean (3.46 Ga) hydrothermally altered basaltic rocks exposed near Marble Bar, eastern Pilbara Craton, have been studied in order to reveal geological and geochemical natures of seafloor hydrothermal carbonatization and to estimate the CO2 flux sunk into the altered oceanic crust by the carbonatization. The basaltic rocks are divided into basalt and dolerite, and the basalt is further subdivided into type I, having original igneous rock textures, and type II, lacking these textures due to strong hydrothermal alteration. Primary clinopyroxene phenocrysts are preserved in some part of the dolerite samples, and the alteration mineral assemblage of dolerite (chlorite + epidote + albite + quartz ± actinolite) indicates that the alteration condition was typical greenschist facies. In other samples, all primary minerals were completely replaced by secondary minerals, and the alteration mineral assemblage of the type I and type II basalts (chlorite + K-mica + quartz + carbonate minerals ± albite) is characterized by the presence of K-mica and carbonate minerals and the absence of Ca-Al silicate minerals such as epidote and actinolite, suggesting the alteration condition of high CO2 fugacity. The difference of the alteration mineral assemblages between basalt and dolerite is probably attributed to the difference of water/rock ratio that, in turn, depends on their porosity.Carbonate minerals in the carbonatized basalt include calcite, ankerite, and siderite, but calcite is quite dominant. The δ13C values of the carbonate minerals are −0.3 ± 1.2‰ and mostly within the range of marine carbonate, indicating that the carbonate minerals were formed by seafloor hydrothermal alteration and that carbonate carbon in the altered basalt was derived from seawater. Whole-rock chemical composition of the basaltic rocks is essentially similar to that of modern mid-ocean ridge basalt (MORB) except for highly mobile elements such as K2O, Rb, Sr, and Ba. Compared to the least altered dolerite, all altered basalt samples are enriched in K2O, Rb, and Ba, and are depleted in Na2O, reflecting the presence of K-mica replacing primary plagioclase. In addition, noticeable CO2 enrichment is recognized in the basalt due to the ubiquitous presence of carbonate minerals, but there was essentially neither gain nor loss of CaO. This suggests that the CO2 in the hydrothermal fluid (seawater) was trapped by using Ca originally contained in the basalt. The CaO/CO2 ratios of the basalt are generally the same as that of pure calcite, indicating that Ca in the basalt was almost completely converted to calcite during the carbonatization, although Mg and Fe were mainly redistributed into noncarbonate minerals such as chlorite.The carbon flux into the Early Archean oceanic crust by the seafloor hydrothermal carbonatization is estimated to be 3.8 × 1013 mol/yr, based on the average carbon content of altered oceanic crust of 1.4 × 10-3 mol/g, the alteration depth of 500 m, and the spreading rate of 1.8 × 1011 cm2/yr. This flux is equivalent to or greater than the present-day total carbon flux. It is most likely that the seafloor hydrothermal carbonatization played an important role as a sink of atmospheric and oceanic CO2 in the Early Archean. 相似文献
12.
塔里木盆地北部下奥陶统碳酸盐岩孔洞充填物特征及其成岩环境分析 总被引：2，自引：0，他引：2
为了正确分析和评价碳酸盐岩溶蚀孔洞在埋藏成岩环境中的发育和保存条件,对塔里木盆地北部露头剖面中下奥陶统白云岩及其溶蚀孔洞的充填物进行了详细的矿物学和地球化学研究,试图对这类孔洞充填物沉淀时的成岩环境进行恢复。大型洞穴充填物的矿物学特征和微孔洞充填物扫描电镜的分析表明,此类孔洞的环带状充填物具有明显的世代性,由基岩向孔洞中心,至少可识别出4期充填物,即第1期的乳白色白云石,第2期的铁质浸染的杂色高镁方解石,第3期的无色透明白云石和第4期的自形石英。碳、氧同位素分析结果表明,孔洞充填物形成于高温条件,结合微量元素、稀土元素所示的成岩信息可进一步推断其形成于高温埋藏环境,而非现代表生暴露期的充填物;第1期和第3期白云石充填物形成在相对还原且高盐度的流体性质条件下,而第2期高镁方解石充填物沉淀时相对偏氧化,盐度也偏低。据下奥陶统此类4期充填物的特征分析可知,第2期高镁方解石充填物的发育可能与构造抬升导致成岩环境的改变有关。 相似文献
13.
At Telões, a subaluminous medium- to coarse-grained porphyritic biotite granite, crops out along the Vila Real NNE–SSW fault. It is a post-tectonic granite of 299±3 Ma old given by U–Pb isotopic data on zircon. It contains metaluminous to subaluminous tonalitic, granodioritic and monzogranitic enclaves. All granitoids have Fe2+-biotite and some enclaves contain magnesiohornblende and subsolidus actinolite. Monzogranitic enclaves show obvious similarities to the host granite. Linear array between enclaves and host granite is observed in Rb–Sr typical isochron diagram and gives the age of 286±11 Ma and (87Sr/86Sr)0=0.7063±0.0011. Microgranular enclaves have δ18O values similar to those of the hosting granite. Microgranular enclaves are hybrid rocks probably formed by mixing between a tonalitic enclave magma and a host granite magma as supported by the modelling of major and trace elements. The similar isotopic signatures suggest a subsequent partial equilibration of the enclaves and granite magmas. 相似文献
14.
Maria Luce Frezzotti Tom Andersen Else-Ragnhild Neumann Siri Lene Simonsen 《Lithos》2002,64(3-4):77-96
Three types of fluid inclusions have been identified in olivine porphyroclasts in the spinel harzburgite and lherzolite xenoliths from Tenerife: pure CO2 (Type A); carbonate-rich CO2–SO2 mixtures (Type B); and polyphase inclusions dominated by silicate glass±fluid±sp±silicate±sulfide±carbonate (Type C). Type A inclusions commonly exhibit a “coating” (a few microns thick) consisting of an aggregate of a platy, hydrous Mg–Fe–Si phase, most likely talc, together with very small amounts of halite, dolomite and other phases. Larger crystals (e.g. (Na,K)Cl, dolomite, spinel, sulfide and phlogopite) may be found on either side of the “coating”, towards the wall of the host mineral or towards the inclusion center. These different fluids were formed through the immiscible separations and fluid–wall-rock reactions from a common, volatile-rich, siliceous, alkaline carbonatite melt infiltrating the upper mantle beneath the Tenerife. First, the original siliceous carbonatite melt is separated from a mixed CO2–H2O–NaCl fluid and a silicate/silicocarbonatite melt (preserved in Type A inclusions). The reaction of the carbonaceous silicate melt with the wall-rock minerals gave rise to large poikilitic orthopyroxene and clinopyroxene grains, and smaller neoblasts. During the metasomatic processes, the consumption of the silicate part of the melt produced carbonate-enriched Type B CO2–SO2 fluids which were trapped in exsolved orthopyroxene porphyroclasts. At the later stages, the interstitial silicate/silicocarbonatite fluids were trapped as Type C inclusions. At a temperature above 650 °C, the mixed CO2–H2O–NaCl fluid inside the Type A inclusions were separated into CO2-rich fluid and H2O–NaCl brine. At T<650 °C, the residual silicate melt reacted with the host olivine, forming a reaction rim or “coating” along the inclusion walls consisting of talc (or possibly serpentine) together with minute crystals of NaCl, KCl, carbonates and sulfides, leaving a residual CO2 fluid. The homogenization temperatures of +2 to +25 °C obtained from the Type A CO2 inclusions reflect the densities of the residual CO2 after its reactions with the olivine host, and are unrelated to the initial fluid density or the external pressure at the time of trapping. The latter are restricted by the estimated crystallization temperatures of 1000–1200 °C, and the spinel lherzolite phase assemblage of the xenolith, which is 0.7–1.7 GPa. 相似文献
15.
Origin and granite alteration effects of hydrothermal fluid: isotopic evidence from fluorite veins, Co. Galway, Ireland 总被引：1，自引：0，他引：1
The Costelloe Murvey Granite is a chemically evolved, high heat production, leucocratic component of the 400 Ma old Galway
Granite batholith and is host to hydrothermal fluorite-quartz-calcite veins. A previously reported clinopyroxene 40Ar-39Ar age of 231±4 Ma obtained from a pre-mineralization dolerite dyke is reinterpreted as dating this mineralization. The hydrothermal
fluid extensively altered its granite wallrocks, leading to lower Sm and Nd and higher Rb concentrations in altered granite,
disturbing both its Rb-Sr and Sm-Nd isotopic systems. The 87Sr/86Sr ratio of the hydrothermal fluid from which fluorite and calcite precipitated ranged from 0.7101 to 0.7139. These ratios
are very much lower than in the Costelloe Murvey Granite at the time of mineralization, precluding the granite as a source
for more than 2% of the hydrothermal Sr. The initial 143Nd/144Nd ratio varies between fluorite in different veins due to Nd derivation from local wallrocks, and between fluorite of petrographically
distinct growth phases within a single hand specimen, highlighting the difficulty of Sm-Nd isochron dating of fluorite in
cases where there are multiple sources of hydrothermal Nd. It is proposed that fluorite and calcite precipitated where hot,
dilute fluids rising through the granite mixed with cooler, more saline fluids of basinal origin migrating through Lower Carboniferous
limestone which then overlay the granite.
Received: 3 August 1995 / Accepted: 11 April 1996 相似文献
16.
《Applied Geochemistry》1999,14(7):953-962
Isotopic compositions of C (δ13C), O (δ18O) and Sr (δ87Sr) were determined for calcite fracture fillings in the crystalline rock penetrated by a 1.6 km drill hole at Laxemar, near the Äspö Hard Rock Laboratory (ÄHRL) in southern Sweden. These calcites precipitated from groundwater some time in the past, and their δ13C, δ18O and δ87Sr values reflect those of the source waters. The present-day groundwater system is hydrochemically stratified with highly saline water underlying more shallow brackish and fresh water. The origin of this stratified system is probably related to past glaciations although the ultimate origin of the deep, highly saline water is still problematical. None of the calcite fracture fillings sampled below 900 m could have precipitated from any of the present-day ground waters which in view of the glacial history of the region is not surprising. However, several shallow calcite fracture fillings are formed by precipitation from the present-day groundwater. Coupled variations in δ13C, δ18O and δ87Sr isotopes at depths in excess of 900 m suggest that these isotope systems in calcite are recording a time-dependent evolution of groundwater composition. 相似文献
17.
沉积地层中成矿作用的碳同位素特征和含矿缺氧盆地成因新观点 总被引：2，自引：0，他引：2
沉积盆地内地层中碳的来源 ,根据其碳、氧同位素特征可归纳为 :海洋沉积碳酸盐碳、生物碳、热解非生物成因碳、大气淡水方解石碳和热卤水系统中的无机碳。热水成因的金矿及喷气 沉积矿床中的碳都具有深源成因的无机碳。深部含无机碳的热流体喷溢到海洋底部可以解释为扩张盆地底部形成的缺氧环境和含矿黑色页岩的主导原因 相似文献
18.
沉积盆地内地层中碳的来源,根据其碳,氧同位素特征可归纳为：海洋沉积碳酸盐碳,生物碳,热解非生物成因碳,大气淡水方解石碳和热卤水系统中的无机碳。热水成因的金矿及喷气－沉积矿床中的碳都具有深源成因的无机碳。深部含无机碳的热流体喷溢到海洋底部可以解释为扩张盆地底部形成的缺氧环境和含矿黑色页岩的主导原因。 相似文献
19.
H.-R. Wenk Hu Meisheng T. Lindsey J. W. Morris Jr. 《Physics and Chemistry of Minerals》1991,17(6):527-539
Two rhombohedral carbonates, ferroan dolomite (ankerite) and magnesian calcite from lower Jurassic ammonites, have been studied by transmission electron microscopy. The samples show small domains with the morphology of platelets parallel to (11 \(\bar 2\) 0) which have exceptionally well ordered superstructures and characteristic c-reflections. Diffraction patterns and contrast analysis of atomic resolution images indicate that the domains observed in ankerite are rich in Ca [Ca0.75(Mg, Fe)0.25CO3] and those in calcite rich in Mg, and there is strong evidence that cation ordering is the cause for the observed superstructures which are proposed mainly on diffraction evidence. Rhombohedral carbonates have a close similarity to NaCl, with CO3-groups substituting for Cl. Cation ordering patterns can therefore be discussed in analogy to f.c.c. alloys. We make use of ordering waves to describe superstructures and to qualitatively interpret kinetic conditions for their formation. 相似文献
20.
Takazo Shibuya Tsuyoshi Komiya Kentaro Nakamura Ken Takai Shigenori Maruyama 《Precambrian Research》2010
Based on the petrology of hydrothermally altered Archean basaltic greenstones, thermodynamic calculations of phase equilibria were conducted to estimate the composition of a high-temperature (∼350 °C) hydrothermal fluid in an Archean subseafloor basalt-hosted hydrothermal system. The results indicate that the hydrothermal fluid was highly alkaline attributed to the presence of calcite in the alteration minerals under a high-CO2 condition, and predict a generation of SiO2-rich, Fe-poor hydrothermal fluids in the Archean subseafloor hydrothermal system. The chemically reactive mixing zones between alkaline hydrothermal fluids and slightly acidic-neutral seawater are characterized by inverse pH and chemical polarity to modern hydrothermal systems, leading to extensive precipitation of silica and iron oxyhydroxides on/under the seafloor. Such processes can be responsible for the abiotic formation of voluminous chert and subseafloor silica dike, the mechanism of silicification, and the pH-controlled generation of banded iron formation that has been arising mainly from the redox chemistry in the Archean ocean. Such high-temperature alkaline fluids could have had a significant role not only in the early ocean geochemical processes but also in the early evolution of life. 相似文献