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1.
The Fairholme carbonate complex is part of the extensively dolomitized Upper Devonian carbonate reefs in west-central Alberta. The studied formations contain moulds (up to 10 cm in diameter), which are filled partially with (saddle) dolomite, quartz and calcite cements. These cements precipitated from a mixture of brines that acquired high salinity by dissolution of halite and brines derived from evaporated sea water. The fluids were warm (homogenization temperature of primary fluid inclusions of 76 to 200 °C) and saline (20 to 25 wt% NaCl equivalent) and testify to thermochemical sulphate reduction processes. The latter is deduced from S in solid inclusions, CO2 and H2S in volatile-rich aqueous inclusions and depleted δ13C values down to −26‰ Vienna Pee Dee Belemnite. High 87Sr/86Sr values (0·7094 to 0·7110) of the cements also indicate interaction of the fluids with siliciclastic sequences. The thermochemical sulphate reduction-related cements probably formed during early Laramide burial. Another (younger) calcite phase, characterized by depleted δ18O values (−23·9‰ to −13·9‰ Vienna Pee Dee Belemnite), low Na (27 to 37 p.p.m.) and Sr (39 to 150 p.p.m.) concentrations and non-saline (∼0 wt% NaCl equivalent) fluid inclusions, is attributed to post-Laramide meteoric water.  相似文献   

2.
Nine stratigraphic sections, each ≈5 m thick, were sampled from the Alamogordo Member limestones of the Lake Valley Formation, Sacramento Mountains, New Mexico, USA. Four stratigraphic sections consist entirely of lime mudstone and wackestone, whereas the other five sections have a prominent layer of crinoidal packstone about 1 m thick at their base. Stable isotopic analyses reveal that the lime muds in the sections with basal packstone layers show a downward decrease in δ18O and constant δ13C values, whereas those in the sections solely composed of lime mudstone and wackestone have, in general, relatively uniform δ18O and δ13C values. The diagenesis of the Alamogordo Member limestones was previously believed to have been governed by the downward percolation of meteoric water from a regional pre-Pennsylvanian exposure surface ≈100 m above this unit. However, the uniform δ13C and downward decrease in δ18O values in the lime muds in the sections with basal packstones indicate that the meteoric water ascended within the Alamogordo Member, rather than descended from the overlying exposure surface. This indicates that the basal packstones were probably a conduit for meteoric water. This is further supported indirectly by the relatively uniform δ18O and δ13C values of the lime mud in the sections without basal packstones. The implications are that the oxygen isotopic gradients may be used to identify palaeoaquifers, flow directions within these aquifers and that meteoric diagenesis below an exposure surface could be governed by flow through a palaeoaquifer.  相似文献   

3.
Abstract. Granitic rocks related to the formation of Haobugao Zn-Pb-Cu-Sn skarn deposit, Inner Mongolia, China, show unusual low whole-rock δ18O values down to -8.8 % (V-SMOW), whereas separated quartz crystals from those rocks give positive δ18O values of+4.1 to +9.9 %. Chemical analyses and microscopic observation of those granitic rocks confirm that they suffered hydrothermal alteration. Some skarn specimens and quartz from the Haobugao deposit also show negative δ18O values. The isotopic evidence indicates that intensive meteoric water circulation occurred at the time of granitic intrusion, and caused the pervasive hydrothermal alteration of granitic rocks and the precipitation of skarn deposit in this area.  相似文献   

4.
Calcite and quartz veins have formed, and are forming, in steeply dipping fissures in the actively rising Alpine Schist metamorphic belt of New Zealand. The fluids that deposited these minerals were mostly under hydrostatic pressure almost down to the brittle-ductile transition, which has been raised to 5-6 km depth by rapid uplift. Some fluids were trapped under lithostatic pressures. Fluids in the fissure veins were immiscible H2O + NaCl-CO2 mixtures at 200-350 C. Bulk fluid composition is 15-20 mol% CO2 and <4.3 total mol CH4+ N2+ Ar/100mol H2O. Water hydrogen isotopic ratio δDH2O in the fissure veins spans -29 to -68‰, δ18OH2O -0.7 to 8.5‰, and bulk carbon isotopic ratio δ13C ranges from -3.7 to -11.7‰. The oxygen and hydrogen isotopic data suggest that the water has a predominantly meteoric source, and has undergone an oxygen isotope shift as a result of interaction with the host metamorphic rock. Similar fluids were present during cooling and uplift. Dissolved carbon is not wholly derived from residual metamorphic fluids; part may be generated by oxidation of graphite.  相似文献   

5.
Abstract. Carboniferous-Permian limestones of the Akiyoshi Plateau, in the Inner Zone of southwestern Japan, are composed of essentially pure calcium carbonate containing only small amounts of other elements, and they are accompanied by marble and copper skarn deposits near the contact with late Cretaceous granitoids. The δ18O values of the Akiyoshi limestones range widely from 7.6 to 28.3% and are mostly lower than those of other areas of the same age (23–29%), whereas the differences among the δ13C values are small. The δ18O values are negatively correlated with Mn and Fe contents. Samples with high δ18O (>25%) and δ13C (>2%) values do not contain Fe, Zn, or Pb, but those with low δ18O values tend to be rich in these elements, indicating that these elements were introduced by interaction with H2O dominant fluids, possibly of magmatic origin. Potential scores for evaluating the degree of interaction with hydro thermal fluids were calculated for δ18O, δ13C, Fe, Mn, Zn, Pb, and Sr. Higher scores implying much hydrothermal interaction were evident in the Mt. Hananoyama area, where there are many skarn deposits, and along faults oriented mainly NNW-SSE. Therefore, these are promising areas for exploring for blind deposits. It is likely that the hydrothermal fluid traveled through the limestones along fractures at the time of the granitic intrusions. However, the potential scores here are much smaller than those in the Pb-Zn mineralized area of the Kamioka mine, so more detailed petrological and mineralogical investigations are necessary.  相似文献   

6.
Abstract: The physical and chemical mechanism of gold precipitation in the typical low-sulfidation epithermal gold deposit at the Hishikari mine was quantified by submillimeter scale oxygen isotope analyses of vein quartz. In situ CO2 laser-ablated fluorination was used to measure temporal δ18O excursions. The calculated oxygen isotopic compositions of the ore-forming fluid indicate a dynamic process of epithermal vein formation. Intermittent opening of the vein allowed introduction of metal-bearing deep fluid to the epithermal system, and associated boiling and subsequent mixing with meteoric water caused precipitation of precious metals.  相似文献   

7.
A breccia vein sampled from a shear zone in greenschist facies metapelites at Mount Isa, Queensland, Australia, shows a systematic variation in vein geometry that is related to the geometry of folding and faulting within the sample. Calcite vein-fill is coarse grained and equigranular, suggesting precipitation in a fluid-filled space. Partially folded veins suggest that veining occurred during folding and faulting. The breccia vein contains a central zone in which dilation has occurred simultaneously in all directions in the plane of section, implying that this was a zone of high fluid pressure and nearly isostatic differential stress during folding and faulting. From these observations, it can be inferred that the breccia vein was a zone of high permeability and a likely fluid channel during deformation. This hypothesis was tested by stable isotope analysis of veins and host rocks. The calcite veins have δ13C values of -11.1 ± 0.1% and δ18O values of 6-10%o, whereas the host metapelite has δ13C values of -10.62 and -10.11% and δ18O values of 14-15%o. These values are consistent with an igneous-derived, H2O-dominated fluid that exchanged little oxygen with the host rocks, but derived much of its carbon from the wall rock. The isotopic disequilibrium between the veins and the wall rock confirms that the fluid was externally derived, and that the breccia vein acted as a channel for large-volume fluid flow within the shear zone.  相似文献   

8.
Abstract. The Onsen site is an active submarine hydrothermal system hosted by the Desmos caldera in the Eastern Manus Basin, Papua New Guinea. The hydrothermal fluid is very acidic (pH=1.5) and abundant native sulfur is deposited around the vent. The δ34S values of native sulfur range from -6.5 to -9.3 %o. δ34S values of H2S and SO4 in the hydrothermal fluid are -4.3 to -9.9 %o and +18.6 to +20.0 %o, respectively. These δ34S values are significantly lower than those of the other hydrothermal systems so far reported. These low δ34S values and the acidic nature of the vent fluids suggest that volcanic SO2 gas plays an important role on the sulfur isotope systematic of the Onsen hydrothermal system. Relationship among the δ34S values of S-bearing species can be successively explained by the model based on the disproportionation reaction starting from the volcanic SO2 gas. The predicted δ34S values of SO2 agree with the measured whole rock δ34S values. δD and δ18O values of clay minerals separated from the altered rock samples also suggest the contribution of the magmatic fluid to the hydrothermal system. Present stable isotopic study strongly suggests that the Onsen hydrothermal site in the Desmos caldera is a magmatic submarine hydrothermal system.  相似文献   

9.
Refinements have been made to achieve over 99% yield in the conversion of CO to CO2 in order to improve the reproducibility and accuracy of δ18 O measurements in sulfates. BaSO4 (10-15 mg) was mixed with an identical amount of spectrographic-grade graphite and loaded into a Pt boat. The mixture was gradually heated to 1100 °C to reduce sulfate to CO and CO2; the former gas was simultaneously converted to CO2 by a glow discharge between Pt electrodes immersed in a magnetic field (produced by a pair of external neodymium magnets). A small memory effect was noticed during the analysis (less than 0.3‰ per 10‰ difference in δ18 O between two subsequently analysed samples). The memory effect, however, was suppressed by repetitive preparation of the same specimen. CO2 produced in this way from sulfate reference samples was analysed on a dual inlet and triple collector mass spectrometer along with CO2 equilibrated with VSMOW, GISP and SLAP water reference samples. To avoid large departures of measured isotope ratios from 18O/16O of the working calibrator we used CO2 gas prepared from ocean water sulfate for this purpose. The calibrated δ18 O values (in ‰) obtained in this way for NBS-127, IAEA SO-5 and IAEA SO-6 reference materials were 8.73 ± 0.05, 12.20 ± 0.07 and -10.43 ± 0.12, respectively.  相似文献   

10.
Abstract Fluids, some of which are CO2-rich (up to 40 mol.% CO2) and some of which are highly saline (up to 18 wt% NaCl equivalent), are trapped as fluid inclusions in quartz-calcite (∼ metallic minerals) veins which cross-cut the pumpellyite-actinolite to amphibolite facies rocks of the Alpine Schist. Fluids were commonly trapped as immiscible liquid-vapour mixes in quartz and calcite showing open-space growth textures. Fluid entrapment occurred at fluid pressures near 500 bars (possibly as low as 150 bars) at temperatures ranging from 260 to 330° C. Saline fluids may have formed by partitioning of dissolved salts into an aqueous phase on segregation of immiscible fluids from a low-density CO2-rich fluid. Calcite deposited by these fluids has δ13C ranging from – 8.4 to – 11.5 and δ18O from + 4 to + 13. Isotopic data, fluid compositions and mode of occurrence suggest that the fluids are derived from high-grade metamorphic rocks. Fluid interaction with wall-rock has caused biotite crystallization and/or recrystallization in some rocks and retrogression of biotite to chlorite in other rocks.
Fluid penetration through the rock is almost pervasive in many areas where permeability, probably related to Alpine Fault activity, has focussed fluids on a regional scale into fractured rocks. The fluid flow process is made possible by high uplift-rates (in excess of 10 mm/year) bringing hot rocks near to the surface.  相似文献   

11.
Large amounts of fluid, bound up in the hydrated upper layers of the ocean crust, are consumed at convergent margins and released in subduction zones through devolatilization. The liberated fluids may play an integral role in subduction zone processes, including the generation of arc-magmas. However, exhumed subduction zone rocks often record little evidence of large-scale fluid flow, especially at deeper levels within the subduction zone. Basaltic pillows from the high-pressure Corsican and Zermatt-Saas ophiolites show a range of δ18O values that overall reflect seafloor alteration prior to subduction. However, comparison between the δ18O values of the cores and rims of the pillows suggests that the δ18O values of the pillow rims at least have been modified during subduction and high-pressure metamorphism. Pillows that have not undergone high-pressure metamorphism generally have rims with higher δ18O values than their cores, whereas the converse is the case in pillows that have undergone high-pressure metamorphism. This reversal in the core to rim oxygen isotope relationship between unmetamorphosed and metamorphosed pillows is strong evidence for fluid–rock interaction occurring during subduction and high-pressure metamorphism. However, the preservation of different δ18O values in the cores and rims of individual pillows and within and between different pillows suggests that fluid flow within the subduction zone was strongly channelled. Resetting of the δ18O values in the pillow rims was probably due to fluid-hosted diffusion that occurred over relatively short time-scales (<1 Myr).  相似文献   

12.
The carbon (δ13 C) and oxygen (δ18O) isotopic composistion in mollusc shells in mainly determined by the isotopic composition of water and dissolved bicarbonate. The δ18O values of water show a good correlation with the salinity of the Baltic. This correlation served as a basis for reconstructing palaeosalinity and for stratifying the marine sediments according to the δ18O values of the carbonate skeletons of subfossil shells. The δ13C values in shells are mainly determined by the isotopic composition of land-originating bicarbonate, especially in the carbonate skeleton of Lymnaea balthica , which inhabits the immediate coastal zone. According to the δ18O data, salinity in the investigated area (the coastal area of W and NW Estonia) was highest (about 9–11%) during the Littorina stage. The Limnae a stage had, in general, a salinity similar to the contemporary one, but during some phases possibly exceeding it by 2–3%.  相似文献   

13.
Abstract: Interstitial water expelled from gas hydrate-bearing and -free sediments in the Nankai Trough are analyzed in terms of Cl-, SO42-, δ18O and δD. The baselines for the Cl- concentration and δ18O value are close to seawater values (530 mM and 0%), indicating that the interstitial water is of seawater origin. The δD values decrease with depth, implying isotopic exchange of hydrogen between upwelling biogenic methane depleted in D and interstitial water. The Cl- concentrations in gas hydrate-bearing sediments are anomalously low, while the δ18O and δD values are both high, suggesting that the water forming these gas hydrates was poor in Cl- and enriched in 18O and D during gas hydrate formation. Calculation of the gas hydrate saturations using Cl "and δ18O anomalies gives results of up to 80 % in sand, and shows that the δ18O baseline is not consistent with the Cl" baseline. The δ18O baseline increases by +1% in gas hydrate-free clay and silt. This is considered to be caused by clustering of water molecules after gas hydrate dissociation in response to the upward migration of the base of gas hydrate stability, as indicated by the presence of a double bottom-simulating reflector at this site. The water clusters enriched in 18O are responsible for the increase in the δ18O baseline with normal Cl". The abrupt shallowing of the base of gas hydrate stability may induce the dissociation of gas hydrates and the accumulation of gases in the new stability zone, representing a geological process that increases gas hydrate saturation.  相似文献   

14.
The Archean mafic–ultramafic complex of Lac des Iles, Ontario, Canada, hosts economic platinum group elements (PGE)-Au-Cu-Ni mineralization in the Roby Zone. All lithologies in the North Roby Zone have been affected by hydrothermal alteration. The alteration products include talc (the most dominant mineral), anthophyllite, serpentine, actinolite, tremolite, chlorite, hornblende, zoisite, clinozoisite, epidote and sericite. In the altered rocks, light rare earth elements (La, Ce, Nd, Sm), Pb, Rb, Ba, Cs, S and possibly Y have been added by hydrothermal solution whereas Eu and heavy rare earth elements (Yb, Gd, Dy, Er) remained immobile. There are five types of fluid inclusions in the pegmatitic plagioclase with homogenization temperature and salinity ranging from 240°C to 445°C and 15.37 to 48.52 wt% equivalent NaCl, respectively. The δ18O and δD of talc range form 6.2‰ to 6.9‰ and −28‰ to −48‰, respectively. δ18O and δD water in equilibrium with talc during the hydrothermal alteration suggest a modified source for the hydrothermal solution. Microthermometry and stable isotope studies suggest that high temperature–high salinity fluid was diluted by, and mixed with, low temperature–low salinity meteoric solution. This mechanism precipitated the hydrothermal assemblage and redistributed trace elements during and after pegmatite formation in the North Ruby Zone.  相似文献   

15.
Oxygen isotope exchange and closure temperatures in cooling rocks   总被引：3，自引：0，他引：3  
Retrograde exchange of oxygen isotopes between minerals in igneous and metamorphic rocks by means of diffusion is explored using a finite difference computer model, which predicts both the zonation profile of δ18O within grains, and the bulk δ18O value of each mineral in the rock. Apparent oxygen isotope equilibrium temperatures that would be observed in these rocks are calculated from the δ18O values of each mineral pair within the rock. In systems which cool linearly from a sufficiently high temperature or at a low enough cooling rate, such that the final oxygen isotope values are not dependent upon the initial oxygen isotope values ('slow cooling'), the apparent oxygen isotope temperature derived for a rock composed of a single mineral pair can be shown to be simply related to the Dodson closure temperatures ( T c) for the two phases and the mode of the rock. Adding a third phase into a system which undergoes 'slow' cooling will cause the apparent temperature derived for the two minerals already present to differ from the simple relationship for a two-phase system. In some systems oxygen isotope reversals can be developed. If cooling is not 'slow', then the mineral δ18O values resulting from cooling will be partly dependent upon the initial temperature of the system concerned. The model successfully simulates the mineral δ18O values that are often observed in granitic rocks. Application of the model will help in assessing the validity of oxygen isotope thermometry in different geological settings, and allows quantitative prediction of the oxygen isotope fractionations that are developed in cooling closed systems.  相似文献   

16.
Abstract Quartz-hosted, synthetic CO2-H2O fluid inclusions behave as open systems with respect to diffusional transfer of hydrogen during laboratory-simulated metamorphic re-equilibration at 650, 750 and 825°C and 1.5 kbar total pressure with fO2 defined by the C-CH4 buffer. Microthermometry and Raman spectroscopy show that the initial CO2-H2O inclusions become CO2-CH4-H2-H2O
inclusions after diffusive influx of hydrogen from the reducing confining medium. Measurable changes are observed in inclusion compositions after only 15 days of re-equilibration, implying significant hydrogen mobility at still lower temperatures over geological time spans. Results of synthetic inclusion re-equilibrium experiments have profound implications for the interpretation of natural fluid-inclusion data; failure to account for potential hydrogen migration in inclusions from high-temperature geological environments may lead to erroneous estimates of P-T, and/or the compositions of metamorphic fluids.  相似文献   

17.
荒沟山金矿床为吉南老岭金-多金属成矿带内较具代表性矿床之一,产于元古宇老岭群珍珠门组地层之中,受韧性剪切带构造控制.按地质特征、矿物组合及矿脉之间的穿切关系,将荒沟山金矿床热液成矿作用划分为Ⅰ黄铁矿-毒砂-石英阶段和Ⅱ晚期辉锑矿-乳白色石英两个阶段.系统的流体包裹体岩相学及显微测温研究表明:Ⅰ阶段石英中发育含CO2三相、碳质及气液两相3种类型的原生流体包裹体,成矿流体属不混溶的中低温、低盐度NaCl-H2O-CO2体系热液,在成矿过程中发生过不混溶作用而导致金等有用元素沉淀富集;Ⅱ阶段石英颗粒中主要发育气液两相包裹体,成矿流体属均匀的NaCl-H2O体系热液.碳、氢、氧同位素研究表明,Ⅰ阶段成矿流体主要来源于岩浆热液,Ⅱ阶段流体除继承早阶段的热液外,还有大气降水的混入;δD和δ13CV-PDB值分析结果证明两个成矿阶段流体均与地层发生过较强的水岩反应.矿床成因属于中温岩浆热液矿床.   相似文献   

18.
One-dimensional advection-dispersion models predict that characteristic δ18O vs. distance and δ18O vs. δ13C profiles should be produced during isothermal metamorphic fluid flow under equilibrium conditions. However, the patterns of isotopic resetting in rocks that have experienced fluid flow are often different from the predictions. Two-dimensional advection-dispersion simulations in systems with simple geometries suggest that such differences may be as a result of fluid channelling and need not indicate disequilibrium, high dispersivities, or polythermal flow. The patterns of isotopic resetting are a function of: (1) the permeability contrast between more permeable layers ('channels') and less permeable layers ('matrix'); (2) the width and spacing of the channels; (3) the width and spacing of discrete fractures; and (4) the orientation of the pressure gradient with respect to layering. In fractured systems, the efficiency of isotopic transport depends on the fracture aperture and the permeability of the surrounding rock. Resetting initially occurs along and immediately adjacent to the fractures, but with time isotopic resetting because of flow through the rock as a whole increases in importance. Application of the one-dimensional advection-dispersion equations to metamorphic fluid flow systems may yield incorrect estimates of fluid fluxes, intrinsic permeabilities, dispersivities, and permeability contrasts unless fluid flow occurred through zones of high permeability that were separated by relatively impermeable layers.  相似文献   

19.
红岭铅锌矿是内蒙古东南部的大型代表性矿床之一.目前,对该矿床成矿流体地球化学特征、性质及演化问题尚缺乏系统研究.对其展开了系统的流体包裹体研究.结果表明,矿区矽卡岩期Ⅰ阶段石榴石中发育含NaCl子矿物三相(SL)、气相-富气相(LV)及气液两相(VL)3种类型的原生流体包裹体,Ⅱ阶段中石英颗粒主要发育LV和VL两种类型原生流体包裹体,测温结果表明矽卡岩期成矿流体属中-高温、高盐度的不均匀NaCl-H2O体系热液,在成矿过程中发生过沸腾作用而导致铅、锌、铜等有用元素沉淀富集.石英-硫化物期Ⅲ→Ⅵ阶段中矿物均主要发育较单一的VL型包裹体,其中Ⅲ阶段热液均一温度较矽卡岩期明显降低,而盐度没有明显变化;Ⅳ阶段成矿流体均一温度明显增高、盐度明显降低,反映了有新的高温、低盐度体系热液的加入;而Ⅴ→Ⅵ阶段成矿流体均一温度及盐度逐渐降低,体现了一种不断与外来天水混合的演变趋势;整体上看,石英-硫化物期流体为简单的中-低温、低盐度NaCl-H2O体系热液.流体包裹体C、H、O同位素研究表明,红岭矿床矽卡岩期Ⅱ阶段成矿流体以岩浆水为主;石英-硫化物期成矿流体源自大气降水与岩浆水的混合流体,晚阶段逐渐演化为以大气降水为主.矿床S、Pb同位素研究表明,区内成矿物质具深源特点.   相似文献   

20.
Results of electron microprobe and microthermometric studies of samples collected from the Bouvet Triple Junction Region (BTJR) during a joint Russian-Italian geological expedition on the R/V Academician Nikolaj Strakhov (1994) have revealed new data on the composition of basaltic magmas and oceanic hydrothermal fluids connected with magmatic processes. Detailed analysis of basaltic glasses shows that the modem Mid-Atlantic Ridge (MAR) rift valley is composed of normal mid-ocean ridge basalts with low concentrations of K2 O and TiOz (N-MORB), while its flanks are more enriched with these components approaching E-MORB. A marked influence of the Bouvet hot spot volcanism on magma generation on the South-West Indian Ridge (SWIR) near Bouvet Island is observed. Basaltic melts in this area belong to alkalic and transitional series and have maximum contents of K2O, TiO2, H2O.
Microthermometric analyses of fluid inclusions in the samples from the BTJR have revealed major differences in the oceanic hydrothermal fluid systems on the MAR and near SWIR, which depends on the peculiarities of magma. In the area of the MAR (with dry melts) only H2O solution inclusions in quartz were found; thus, seawater is probably the only primary source of hydrothermal fluids (NaCl + MgCl2+ H2O; T = 170–200°C). In the SWIR area (with the high content of water in melts) syngenetic liquid CO2 and H2O solution inclusions in quartz indicate the influence of the magmatic fluid component on the ore-forming water/carbon dioxide solutions (NaCl + CaC12+ H2O + CO2; T = 200–310 °C; P = 900–1700 bar).  相似文献   

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