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1.
The Whitestone Anorthosite (WSA), located in the Central Gneiss Belt of the south-western Grenville Province, Ontario, exhibits a nearly concentric metamorphic envelope characterized by an increase in modal scapolite, hornblende, epidote and garnet, developed around a core of granulite facies clinopyroxene ± orthopyroxene ± garnet meta-anorthosite. Scapolite- and hornblende-bearing assemblages develop mainly at the expense of plagioclase and pyroxene within the envelope. Stable isotopic and petrological data for scapolite-bearing mineral assemblages within meta-anorthosite constrain the source of carbon responsible for CO3-scapolite formation and the extent of fluid/rock interaction between the anorthosite and adjacent lithologies. Stable isotopic data indicate increasing δ18O and δ13C from core to margin of the meta-anorthosite and for samples from the southern extension of the WSA, where it is ductilely deformed within the Parry Sound Shear Zone (PSSZ). The average δ18OSMOW value (whole rock) for the WSA core is 6.9‰, increasing to 11.5‰ where the WSA is in tectonic contact with marble breccia. The average δ13CPBD value of scapolite in meta-anorthosite from the centre of the WSA is -3.4‰, increasing to -0.5‰ at the eastern (marble) contact. Average values of δ13C for scapolite and whole-rock δ18O for samples from the shear zone are -1.0 and 8.0‰, respectively. Marbles have average δ18O and δ13C values of 19.2 and -0.4‰, respectively. The sulphate content of texturally primary scapolite decreases from the core of the WSA (XSO4= 0.48) to the eastern contact (≤0.05). Texturally late scapolite after plagioclase and garnet tends to be CO3-rich relative to texturally primary scapolite, and some scapolite grains show zoning in the anion site with CO3-enriched rims. Scapolite composition may vary at any scale from a single grain to outcrop. The pattern of isotopic enrichment in 13C and 18O preserved in the eastern margin of the WSA is consistent with marble as the major source of fluid contributing to the formation of the metamorphic envelope. The decrease in XSO4 and increase in XCO3 in scapolite toward the margin of the WSA indicate that the volatile content was reset by, or developed from, a CO2-bearing fluid. Assuming derivation of fluid from marble, minimum fluid/rock values at the margin of the WSA range from 0.03 for the least enriched, to 0.30 for the most isotopically enriched samples. Although marble is not found in immediate contact with samples of sheared meta-anorthosite from the PSSZ, a marble source is also consistent with the C and O isotope composition and anion chemistry of scapolite within these samples.  相似文献   

2.
At a total pressure of 5 kb, calcic, Cl-free scapolite (Me83) is stable relative to plagioclase-bearing assemblages at T ≧ 625°C, XCO2 ≧ 0.12. With decreasing temperature, scapolite breaks down to plagioclase + calcite. Scapolite is replaced by plagioclase + grossular + cancrinite + CO2 in the presence of H2O-rich fluids. The stable coexistence of scapolite and calcite, an assemblage typical of most natural occurrences of calcic scapolite, is limited by the reaction: scapolite + calcite → grossular + cancrinite + CO2, which occurs at 750°C, XCO2 = 0.46; 700°C, XCO2 = 0.33; 650°C, XCO2 = 0.18, for the chosen bulk composition.Generalization of the experimental results to encompass the complete range of fully carbonated scapolite compositions indicates that mizzonite (Me75) has the largest T-XCO2 stability field. For scapolite more calcic than mizzonite, stable growth is restricted to conditions of increasingly higher temperature and XCO2.The experimental results are consistent with various petrologic features of scapolite-bearing rocks, particularly scapolite-clinopyroxene granulites, and indicate that such rocks were formed in the presence of CO2-rich fluids.  相似文献   

3.
Synorogenic veins from the Proterozoic Eastern Mount Isa Fold Belt contain three different types of fluid inclusions: CO2-rich, aqueous two-phase and rare multiphase. Inclusions of CO2 without a visible H2O phase are particularly common. The close association of CO2-rich inclusions with aqueous two-phase, and possibly multiphase inclusions suggests that phase separation of low- to -moderate salinity CO2-rich hydrothermal fluids led to the selective entrapment of the CO2. Microthermometric results indicate that CO2-rich inclusions homogenize between –15.5 and +29.9 °C which corresponds to densities of 0.99 to 0.60 g.cm−3. The homogenization temperatures of the associated aqueous two-phase inclusions are 127–397 °C, with salinities of 0.5 to 18.1 wt.% NaCl equivalent. The rarely observed multiphase inclusions homogenize between 250 and 350 °C, and have salinities ranging from 34.6 to 41.5 wt.% NaCl equivalent. Evidence used to support the presence of fluid immiscibility in this study is mainly derived from observations of coexisting H2O-rich and CO2-rich inclusions in groups and along the same trail. In addition, these two presumably unmixed fluids are also found on adjacent fractures where monophase CO2-rich inclusions are closely related to H2O-rich inclusions. Similar CO2-rich inclusions are widespread in mineral deposits in this region, which are simply metal-enriched synorogenic veins. Therefore, we argue that fluid immiscibility caused volatile species such as CO2 and H2S to be lost from liquid, thus triggering ore deposition by increasing the fluid pH and decreasing the availability of complexing ligands. Received: 28 April 1997 / Accepted: 4 January 1999  相似文献   

4.
Unaltered metasediments of the Mary Kathleen Fold Belt are composed predominantly of layered amphibolite-facies scapolitic calc-silicate rocks in which minimal infiltration of externally derived fluids occurred during regional metamorphism. There were substantial differences in volatile activities between different layers in the layered sequences, in particular: a CO2/a H 2 O inferred from reaction progress estimates and analysis of biotite-clinopyroxene-fluid phase relations; a NaCl/a H 2 O inferred from scapolite compositions; and a HCl/a H 2 O inferred from biotite compositions. In one outcrop in which a clinopyroxene-producing reaction dominated, differences in approximate X CO 2of up to 0.25 occurred between several samples collected over 50 metres. Variations in a H 2 O/a HCl of up to one order of magnitude are inferred at 1 to 50 m scales from biotite-Cl contents, and variations in NaCl contents of scapolite from 0.0 to up to 0.6 Cl atoms in the Cl–CO3–SO4 site reflect a large variation of a NaCl in the coexisting fluid at similar scales. Most calcsilicate layers internally buffered fluid compositions in the H2O–CO2–NaCl–HCl system. Local occurrences of NaCl-rich scapolite suggest that some layers may have been in equilibrium with halite during early prograde metamorphism. At peak metamorphic temperatures, disolution of halite was complete but layers containing high-NaCl scapolite continued to buffer fluid at high values of a NaCl. Fluid immiscibility does not appear to have affected the progress of the devolatilization reactions. Although fluid was predominantly internally buffered, moderate quantities of fluid were released by prograde mineral reactions in many layers, up to 30 cm3 fluid per 100 cm3 rock. Numerous episodes of fluid escape were required, probably via microfractures, such that the released fluid did not obviously influence reaction progress in the layers through which it passed. The anomaly of beautifully preserved internal buffering signatures and the requirement for produced fluid locally to pass across layers in a deforming rock sequence suggest that the escaping fluid did not leave any readily observable tracks. This is explained by rapid rates of fracture propogation and fluid migration therein. This internally buffered system contrasts strongly with adjacent calc-silicate rocks that show evidence for infiltration of externally derived fluids at high fluid/rock ratios, and highlights the broad range of fluid behaviour that can be expected in deforming, heterogeneous rock sequences.  相似文献   

5.
Phase equilibria in the ternary system H2O-CO2-NaCl were studied at 800 °C and 9 kbar in internally heated gas pressure vessels using a modified synthetic fluid inclusion technique. The low rate of quartz overgrowth along the `b' and `a' axes of quartz crystals was used to avoid fluid inclusion formation during heating, prior to attainment of equilibrium run conditions. The density of CO2 in the synthetic fluid inclusions was calibrated using inclusions in the binary H2O-CO2 system synthesised by the same method and measured on the same heating-freezing stage. In the two-phase field, two types of fluid inclusions with different densities of CO2 were observed. Using mass balance calculations, these inclusions are used to constrain the miscibility gap and the orientation of two-phase tie-lines in the H2O-CO2-NaCl system at 800 °C and 9 kbar. The equation of state of Duan et al. (1995) approximately describes the P-T section of the ternary system up to about 40 wt% of NaCl. At higher NaCl concentrations the measured solubility of CO2 in the brine is much smaller than predicted by the EOS. A “salting out” effect must be added to the equation of state to include coulomb interaction in the model of Anderko and Pitzer (1993) and Pitzer and Jiang (1996). The new experimental data together with published data up to 5 kbar (Shmulovich et al. 1995) encompass practically all subsolidus crustal P-T conditions. A feature of the new experimental results is the large compositional range in the H2O-CO2-NaCl system occupied by the stability fields of halite + CO2-rich fluid ± H2O-NaCl brine. The prediction of halite stability in equilibrium with CO2-rich fluid in deep-crustal rocks is supported by recent petrological and fluid inclusion studies of granulites. Received: 29 June 1998 / Accepted: 17 March 1999  相似文献   

6.
Fluid infiltration into retrograde granulites of the Southern Marginal Zone(Limpopo high grade terrain)is exemplified by hydration reactions.shear zone hosted metasomatism,and lode gold mineralisation.Hydration reactions include the breakdown of cordierite and orthopyroxene to gedrite kyanite,and anthophyllite,respectively.Metamorphic petrology,fluid inclusions,and field data indicate that a low H_2O-activity carbon-saturated CO_2-rich and a saline aqueous fluid infiltrated the Southern Marginal Zone during exhumation.The formation of anthophyllite after orthopyroxene eslablished a regional retrograde anthophyllite-in isograd and occurred at P-T conditions of- 6 kbar and 610 C,which fixes the minimum mole fraction of II.0 in the CO_2-rich fluid phase at- 0.1.The maximum H_2O mole fraction is hxed by the lower temperature limit(~800℃) for partial melting at ~0.3.C-O-H fluid calculations show that the CO_2-rich fluid had an oxygen fugacity that was 0.6 log10 units higher than that of the fayalite-magnetitequartz buffer and that the CO_2/(CO_2+CH_4) mole ratio of this fluid was 1.The presence of dominantly relatively low density CO_2-rich fluid inclusions in the hydrated granulites indicates that the fluid pressure was less than the lithostatic pressure.This can be explained by strike slip faulting and/or an increase of the rock permeability caused by hydration reactions.  相似文献   

7.
Mid-Proterozoic ( 1000 Ma) granulite facies calc-silicates fromthe Rauer Group, East Antarctica, contain grossular-wollastonite-scapolite-dinopyroxene( + quartz or calcite) assemblages which preserve symplectiteand corona textures typically involving the growth of secondarywollastonite. The textures include (1) wollastonite rims betweenquartz and calcite; (2) wollastonite-plagioclase rims and intergrowthsbetween quartz and scapolite; (3) wollastonite-scapolite-clinopyroxeneinter-growths replacing grossular; and (4) wollastonite-plagioclasesymplectites replacing grossular or earlier symplectites (3). Reactions between grossular, scapolite, wollastonite, calcite,quartz, anorthite, and vapour, have been modelled in the CaO-Al2O3SiO2-H2O-CO2and more complex systems using the internally consistent data-setof Holland & Powell (1990). Reactions producing scapoliteand wollastonite consume vapour as temperature increases (i.e., carbonation), in agreement with the results of Moecher &Essene (1990). These calc-silicates can therefore behave asfluid sinks under high-grade conditions. Conversely, they maybe important fluid sources on cooling and contribute to theformation of post-metamorphic CO2rich fluid inclusions in isobaricallycooled granulites. P-T-CO2 diagrams calculated for typical phase compositions (e.g., garnet, scapolite) demonstrate that the observed texturesare a record of near-isothermal decompression at 800–850 C, consistent with P—rpath determinations based on otherrock types from the Rauer Group. For example, texture (2) resultsfrom crossing the reaction Scapolite + Quartz = Wollastonite + Plagioclase + V on decompression, at 6. 5–7 kb, 820 C, and aCO2 of0–4–0–5. Furthermore, correlations betweenmodes of product phases (e. g., wollastonitexlinopyroxene) andreactant garnet composition preclude open-system behaviour inthe formation of these textures, consistent with post-peak vapour-absentreactions such as Grossular + Calcite + Quartz = Wollastonite + Scapolite occurring on decomposition at high temperatures (>800C). Reaction textures developed in calc-silicates from other granuliteterranes often involve the formation of grossular ( + quartz calcite) as rims on wollastonite-scapolite, or replacementof wollastonite by calcite-quartz. These textures have developedprincipally in response to cooling below 780–810 C andmay be signatures of near-isobaric cooling. Infiltration ofhydrous fluid is not a necessary condition for the productionof garnet coronas in wollastonite-scapolite granulites. *Present address: Department of Earth Sciences, University ofMelbourne, Parkville, Victoria 3052, Australia  相似文献   

8.
The high-pressure granulites of the Uluguru Mountains are part of the Pan-African belt of Tanzania, the metamorphic evolution of which is characterized by an anticlockwise P-T path. Mineral assemblages that represent distinct metamorphic stages are selected for fluid inclusion studies in order to deduce the fluid evolution in metapelites and pyroxene granulites from the prograde to the retrograde stage. Fluid inclusion data improve the petrologically derived P-T path and confirm the anticlockwise evolution. Fluid inclusions in quartz enclosed in garnet porphyroblasts in metapelites preserve prograde fluids of CO2–N2 composition and later-trapped pure CO2. During isochoric heating at temperatures near the peak of metamorphism, deformation and recrystallization led to fluid homogenization yielding N2-poor CO2 composition in the metapelites. Near-peak CO2–N2 fluid inclusions in quartz of metapelites and CO2 inclusions in garnet-pyroxene granulites are characterized by perfect negative crystal shape. Garnet formed in veins and as coronas around orthopyroxene represent the near-isochoric/isobaric cooling stage which is characterized by high-density CO2-rich fluid inclusions. Up to 15 mol% N2 in some primary CO2 inclusions in corona garnet indicate small-scale fluid heterogeneity during the static garnet growth. The fact that high-density fluid inclusions are preserved, suggests a shallow dP/dT slope of the uplift path. Nevertheless, some fluid inclusions decrepitated or re-equilibrated and low-density CO2 inclusions were trapped in the garnet-pyroxene granulite while N2–CH4 inclusions formed in the metapelites. Different fluid compositions in metapelite and metabasite argue for an internal control of the fluid composition by phase equilibria. In shear zones where the pyroxene granulite was transformed into scapolite-biotite schist, CO2–N2 and low-density N2–CH4 fluid inclusions indicate several stages of tectonic activity and suggest fluid influx from the nearby metapelites. High- and low-salinity aqueous inclusions observed beside CO2 inclusions in garnet-pyroxene granulites, in vein quartz and shear zones could be of high-grade origin but are mainly re-equilibrated or re-trapped along healed microfractures during lower-grade stages. Received: 21 May 1997 / Accepted: 6 October 1997  相似文献   

9.
The Archean Shawmere anorthosite lies within the granulite facies portion of the Kapuskasing Structural Zone (KSZ), Ontario, and is crosscut by numerous linear alteration veins containing calcite + quartz ± dolomite ± zoisite ± clinozoisite ± margarite ±paragonite ± chlorite. These veins roughly parallel the trend of the Ivanhoe Lake Cataclastic Zone. Equilibria involving clinozoisite + margarite + quartz ± calcite ± plagioclase show that the vein minerals were stable at T < 600 °C, XCO2 < 0.4 at P ≈ 6 kbar. The stabilities of margarite and paragonite in equilibrium with quartz are also consistent with T < 600 °C and XCO2 < 0.4 at 6 kbar. Additional assemblages consisting of calcite + clinochlore + quartz + talc + margarite indicate T < 500 °C with XCO2 > 0.9. Thus, vein formation, while clearly retrograde, spanned a range of temperatures, and fluid compositions evolved from H2O-rich to CO2-rich. The calcite in the retrograde veins has δ18O values that range from 8.4 to 11.2‰ (average = +9.7 ± 0.9‰) and δ13C values that range from −3.9 to −1.6‰ (average = −3.1 ± 0.6‰). These values indicate that the fluids from which calcite precipitated underwent extensive exchange with the anorthosite and other crustal lithologies. The fluids may have been initially derived either from devolatilization of metamorphic rocks or crystallization of igneous rocks in the adjacent Abitibi subprovince. Vein quartz contains CO2-rich fluid inclusions (final melting T = −57.0 to −58.7 °C) that range in size from 5 to 17 μm. Measured homogenization temperatures (T h) range from −44.0 to 14.5 °C, however for most inclusions (46 of S1), T h = −44.0 to −21.1 °C (ρCO2 ≈ 1.13 to 1.05 g/cm3). At 400 to 600 °C, these densities correspond to pressures of 3.5 to 7 kbar, which is the best estimate of pressures of vein formation. It has been argued that some high density CO2-rich fluid inclusions found in the KSZ were formed during peak metamorphism and thus document the presence of a CO2-rich fluid during peak granulite facies metamorphism (Rudnick et al. 1984). The association of high density CO2-rich fluid inclusions with clearly retrograde veins documents the formation of similar composition and density inclusions after the peak of metamorphism. Thus, the coincidence of entrapment pressures calculated from fluid inclusion density measurements with peak metamorphic pressures alone should not be considered strong evidence for peak metamorphic inclusion entrapment. All fluid inclusion results are consistent with an initially semi-isobaric retrograde P–T path. Received: 2 April 1996 / Accepted: 15 November 1996  相似文献   

10.
Fluid inclusions in garnet, kyanite and quartz from microdiamond-bearing granulites in the Western Gneiss Region, Norway, document a conspicuous fluid evolution as the rocks were exhumed following Caledonian high- and ultrahigh-pressure (HP–UHP) metamorphism. The most important of the various fluid mixtures and daughter minerals in these rocks are: (N2 + CO2 + magnesian calcite), (N2 + CO2 + CH4 + graphite + magnesian calcite), (N2 + CH4), (N2 + CH4 + H2O), (CO2) and (H2O + NaCl + CaCl2 + nahcolite). Rutile also occurs in the N2 + CO2 inclusions as a product of titanium diffusion from the garnet host into the fluid inclusions. Volatiles composed of N2 + CO2 + magnesian calcite characterise the ambient metamorphic environment between HP–UHP (peak) and early retrograde metamorphism. During progressive decompression, the mole fraction of N2 increased in the fluid mixtures; as amphibolite-facies conditions were reached, CH4 and later, H2O, appeared in the fluids, concomitant with the disappearance of CO2 and magnesian calcite. Graphite is ubiquitous in the host lithologies and fluid inclusions. Thermodynamic modelling of the metamorphic volatiles in a graphite-buffered C-O-H system demonstrates that the observed metamorphic volatile evolution was attainable only if the f O2 increased from c. −3.5 (±0.3) to −0.8 (±0.3) log units relative to the FMQ oxygen buffer. External introduction of oxidising aqueous solutions along a system of interconnected ductile shear zones adequately explains the dramatic increase in the f O2. The oxidising fluids introduced during exhumation were likely derived from dehydration of oceanic crust and continental sediments previously subducted during an extended period of continental collision in conjunction with the Caledonian orogeny. Received: 15 December 1997 / Accepted: 25 May 1998  相似文献   

11.
Fluid-calcite-calcite dihedral angles have been measured for fluids in the system H2O−CO2−NaCl, between 1 and 2 kbar, and 550–750° C. It is found that the calcite-calcite-H2O dihedral angle decreases steadily with addition of NaCl from a value of about 80° (pure water) to 44° (60 wt% NaCl). The CO2−H2O system displays a well-defined minimum at , with a dihedral angle of 50°, in contrast to those of pure CO2 and H2O which are 90° and 80° respectively. Experiments containing fluids which are immiscible at run conditions showed a bimodal distribution of dihedral angles in the CO2−H2O−NaCl system, which can be approximately correlated with the compositions of the two fluid phases. Such bimodality was only observed for immiscible fluids in the H2O−NaCl system if the quench rate exceeded about 200°C per min. This is probably due to the extremely rapid establishment of the single phase dihedral angle on quenching. The fluid phase topology in devolatilising marbles will only be a connected network for very saline brines and fluids with close to 0.5. Fluids trapped in fluid inclusions in calcite grains in marbles may be predominantly H2O-rich or CO2-rich, and of low salinity. All other fluid compositions in the H2O−CO2−NaCl-calcite system will occupy isolated pores, the largest of which will grow at the expense of the smallest. Escape of fluid produced during devolatilisation reactions under such conditions will occur by fluid overpressuring and hydrofracture. In contrast, previous experimental studies of quartz-fluid dihedral angles between 950° and 1100° C (Watson and Brenan 1987) predict that quartz-dominated lithologies will permit pervasive flow of H2O−NaCl fluids, but not of H2O−CO2 fluids. Documented geological examples of differences in permeability and fluid flow mechanism between metamorphic argillites, psammites and limestones which support the results of the experimental studies are discussed.  相似文献   

12.
Eclogite-facies rocks and high-pressure granulites provide windows to the deeper parts of subduction zones and the root of mountain chains, carrying potential records of fluids associated with subduction-accretion-collision tectonics. Here, we report petrological and fluid inclusion data on retrogressed eclogite and high-pressure granulite samples from Sittampundi, Kanji Malai and Perundarai in southern India. These rocks occur within the trace of the Cambrian collisional suture which marks the final phase of amalgamation of the Gondwana supercontinent. The garnet–clinopyroxene assemblage in the eclogites preserves relict omphacite, whereas the high-pressure granulites are characterized by an assemblage of garnet and clinopyroxene in the absence of omphacite and with minor plagioclase, orthopyroxene, and quartz. Phase relations computed for the eclogite assemblage yield peak P–T conditions of 19 kbar and 1,010°C. The mafic granulites also preserve the memory of high to ultrahigh-temperature metamorphism followed by an isothermal decompression. Systematic fluid inclusion optical, microthermometric and laser Raman spectroscopic studies were conducted in garnet and plagioclase from the eclogite–high pressure granulite suite. The results suggest that the early fluids were a mixture of CO2, CH4 and N2 probably derived from decarbonation and devolatilization reactions in a subduction setting during the prograde stage. The later generation inclusions, which constitute the dominant category in all the samples studied, are characterized by a near-pure CO2 composition with moderate to high densities (up to 1.154 g/cm3). The highest density fluid inclusions recorded in this study occur within the mafic granulites from Sittampundi (0.968–1.154 g/cm3) and Kanji Malai (1.092–1.116 g/cm3). In some cases, carbonate minerals such as dolomite and calcite are associated with the CO2-rich fluid inclusions. The composition and densities of the later generation fluids closely match with those of the CO2-bearing fluid inclusions reported from ultrahigh-temperature granulites occurring proximal to the eclogite–high pressure granulite suite within this suture zone, and suggest a common tectonic link for the fluid regime. We evaluate the fluid characteristics associated with convergent plate margin processes and propose that the early aqueous fluids probably associated with the eclogites were consumed during the formation of the retrograde hydrous mineral assemblages, whereas the fluid regime of the high-pressure and ultrahigh-temperature granulites was mostly CO2-dominated. The tectonic setting of the rocks along a collisional suture marking the trace along which crustal blocks were welded through subduction–collision process is in favor of a model involving the derivation of CO2 from sub-lithospheric sources such as a carbonated tectosphere invaded by hot asthenosphere, or underplated mafic magmas.  相似文献   

13.
Abstract Fluid inclusion studies of rocks from the late Archaean amphibolite-facies to granulite-facies transition zone of southern India provide support for the hypothesis that CO2,-rich H2O-poor fluids were a major factor in the origin of the high-grade terrain. Charnockites, closely associated leucogranites and quartzo-feldspathic veins contain vast numbers of large CO2-rich inclusions in planar arrays in quartz and feldspar, whereas amphibole-bearing gray gneisses of essentially the same compositions as adjacent charnockites in mixed-facies quarries contain no large fluid inclusions. Inclusions in the northernmost incipient charnockites, as at Kabbal, Karnataka, occasionally contain about 25 mol. % of immiscible H2O lining cavity walls, whereas inclusions from the charnockite massif terrane farther south do not have visibile H2O Microthermometry of CO2 inclusions shows that miscible CH4 and N2 must be small, probably less than 10mol.%combined. Densities of CO2 increase steadily from north to south across the transitional terrane. Entrapment pressures calculated from the CO2 equation of state range from 5 kbar in the north to 7.5 kbar in the south at the mineralogically inferred average metamorphic temperature of 750°C, in quantitative agreement with mineralogic geobarometry. This agreement leads to the inference that the fluid inclusions were trapped at or near peak metamorphic conditions. Calculations on the stability of the charnockite assemblage biotite-orthopyroxene-K-feldspar-quartz show that an associated fluid phase must have less than 0.35 H2O activity at the inferred P and T conditions, which agrees with the petrographic observations. High TiO2 content of biotite stabilizes it to lower H2O activities, and the steady increase of biotite TiO2 southward in the area suggests progressive decrease of aH2O with increasing grade. Oxygen fugacities calculated from orthopyroxene-magnetite-quartz are considerably higher than the graphite CO2-O2 buffer, which explains the absence of graphite in the charnockites. The present study quantifies the nature of the vapours in the southern India granulite metamorphism. It remains to be determined whether CO2-flushing of the crust can, by itself, create large terranes of largeion lithophile-depleted granulites, or whether removal of H2O-bearing anatectic melts is essential.  相似文献   

14.
Non-aqueous CO2 and CO2-rich fluid inclusions are found in the vein quartz hosting mesothermal gold-sulphide mineralization at Bin Yauri, northwestern Nigeria. Although mineralizing fluids responsible for gold mineralization are thought to be CO2-rich, the occurrence of predominantly pure to nearly pure CO2 inclusions is nevertheless unusual for a hydrothermal fluid system. Many studies of similar CO2-rich fluid inclusions, mainly in metamorphic rocks, proposed preferential loss (leakage) of H2O from H2O-CO2 inclusions after entrapment. In this study however, it is proposed that phase separation (fluid immiscibility) of low salinity CO2-rich hydrothermal fluids during deposition of the gold mineralization led to the loss of the H2O phase and selective entrapment of the CO2. The loss of H2O to the wallrocks resulted in increasing oxidizing effects. There is evidence to suggest that the original CO2-rich fluid was intrinsically oxidized, or perhaps in equilibrium with oxidizing conditions in the source rocks. The source of the implicated fluid is thought to be subducted metasediments, subjected to dehydration and devolatilization reactions along a transcurrent Anka fault/shear system, which has been described as a Pan-African (450–750 Ma) crustal suture.  相似文献   

15.
Calc-silicate boudins within Proterozoic granulite facies gneisses of the northern Prince Charles Mountains, East Antarctica, preserve a number of reaction textures including garnet coronas between calcite and scapolite; garnet-quartz coronas between scapolite and wollastonite and between plagioclase and wollastonite; calcite-quartz intergrowths in wollastonite; and calcite-plagioclase symplectites in scapolite. These textures have been modelled using petrogenetic grids for reactions in the CaO-Al2,O3-SiO2-CO2 system, but with reduced mineral activities to account for additional components in real mineral compositions. Such fixed-composition reduced-activity grids are strictly valid only at the point in P-T-aCO2 space where an assemblage last equilibrated, and do not show the true positions of reactions away from this point because mineral compositions change with reaction progress. In this case, however, mineral compositions close to end-member values and low extents of reaction progress mean that compositional change was limited and the grids are good approximations to true pseudosections over the entire P-T-aco2 range of interest. The grids show that the textures are consistent with near-isobaric cooling from about 850 to 700d? C at 7 kbar, a P-T path compatible with thermobarometric studies of other lithologies from the area. Phase relationships indicate that CO2 activities were buffered by the local mineral assemblage during peak and retrograde metamorphism, either under fluid-absent conditions or within a non-pervasive fluid phase. Previous studies of garnet coronas in scapolite-wollastonite calc-silicates have used qualitative grids based on limited experimental data to invoke garnet growth during water infiltration at high temperature, but the grids used here show that garnet coronas can form on cooling, without any need for water influx.  相似文献   

16.
Iron-oxide–Cu–Au deposits, particularly those formed in deeper level (plutonic) environments, are commonly characterized by regional scale sodic(–calcic) alteration, which typically formed pre- or syn-Cu–Au mineralization. The sodic(–calcic) assemblages include albite, scapolite, pyroxene, actinolite, apatite, titanite, epidote and calcite. The consistent presence of coexisting hypersaline aqueous and CO2-rich fluids in minerals from sodic(–calcic) alteration and associated Fe-oxide–Cu–Au deposits is the result of unmixing of H2O–CO2–NaCl ± CaCl2–KCl magmatic fluids. Experimental evidence indicates that the Na/(Na + K) ratio of fluids in equilibrium with two alkali feldspars in CO3 2−-bearing parent fluids would be significantly higher than in unmixed chloride-bearing aqueous fluids. Therefore, fluid unmixing caused by decreases in temperature and/or pressure, will result in albitization of wall rocks, as is observed in most deeper level Fe-oxide–Cu–Au deposits. This alteration style may be succeeded by K-feldspathization with decreasing temperature because of the increase in equilibrium Na/(Na + K) in chloride-bearing fluids buffered by alkali feldspars. Received: 26 May 1999 / Accepted: 8 June 2000  相似文献   

17.
A refined thermodynamic model of H2O and CO2 bearing cordierite based on recent data on volatile incorporation into cordierite (Thompson et al. in Contrib Mineral Petrol 142:107–118, 2001; Harley and Carrington in J Petrol 42:1595–1620, 2001) reflects non-ideality of channel H2O and CO2 mixing. The dependence of cordierite H2O and CO2 contents on P, T and equilibrium fluid composition has been calculated for the range 600–800°C and 200–800 MPa. It has been used for establishing thermodynamic conditions of cordierite formation and the following retrograde P–T paths of cordierite rocks from many localities. Estimates of the H2O and CO2 activities have shown that cordierites in granites, pegmatites and high-pressure granulites were formed in fluid-saturated conditions and wide range of H2O/CO2 relations. Very low cordierite H2O contents in many migmatites may be caused not only by fluid-undersaturated conditions at rock formation and H2O leakage on retrograde P–T paths but also by the presence of additional volatile components like CH4 and N2. The pressure dependence of cordierite-bearing mineral equilibria on fluid H2O/CO2 relations has been evaluated.  相似文献   

18.
Abstract Fluid evolution paths in the COHN system can be calculated for metamorphic rocks if there are relevant data regarding the mineral assemblages present, and regarding the oxidation and nitrodation states throughout the entire P-T loop. The compositions of fluid inclusions observed in granulitic rocks from Rogaland (south-west Norway) are compared with theoretical fluid compositions and molar volumes. The fluid parameters are calculated using a P-T path based on mineral assemblages, which are represented by rocks within the pigeonite-in isograd and by rocks near the orthopyroxene-in isograd surrounding an intrusive anorthosite massif. The oxygen and nitrogen fugacities are assumed to be buffered by the coexisting Fe-Ti oxides and Cr-carlsbergite, respectively. Many features of the natural fluid inclusions, including (1) the occurrence of CO2-N2-rich graphite-absent fluid inclusions near peak M2 metamorphic conditions (927° C and 400 MPa), (2) the non-existence of intermediate ternary CO2-CH4-N2 compositions and (3) the low-molar-volume CO2-rich fluid inclusions (36–42 cm3 mol?1), are reproduced in the calculated fluid system. The observed CO2-CH4-rich inclusions with minor N2 (5 mol%) should also include a large proportion of H2O according to the calculations. The absence of H2O from these natural high-molar-volume CO2-CH4-rich inclusions and the occurrence of natural CH4-N2-rich inclusions are both assumed to result from preferential leakage of H2O. This has been previously experimentally demonstrated for H2O-CO2-rich fluid inclusions, and has also been theoretically predicted. Fluid-deficient conditions may explain the relatively high molar volumes, but cannot be used to explain the occurrence of CH4-N2-rich inclusions and the absence of H2O.  相似文献   

19.
The Southern Marginal Zone of the Limpopo Belt in South Africa is characterised by a granulite and retrograde hydrated granulite terrane. The Southern Marginal Zone is, therefore, perfectly suitable to study fluids during and after granulite facies metamorphism by means of fluid inclusions and equilibrium calculations. Isolated and clustered high-salinity aqueous and CO2(-CH4) fluid inclusions within quartz inclusions in garnet in metapelites demonstrate that these immiscible low H2O activity fluids were present under peak metamorphic conditions (800-850 °C, 7.5-8.5 kbar). The absence of widespread high-temperature metasomatic alteration indicates that the brine fluid was probably only locally present in small quantities. Thermocalc calculations demonstrate that the peak metamorphic mineral assemblage in mafic granulites was in equilibrium with a fluid with a low H2O activity (0.2-0.3). The absence of water in CO2-rich fluid inclusions is due to either observation difficulties or selective water leakage. The density of CO2 inclusions in trails suggests a retrograde P-T path dominated by decompression at T<600 °C. Re-evaluation of previously published data demonstrates that retrograde hydration of the granulites at 600 °C occurred in the presence of H2O and CO2-rich fluids under P-T conditions of 5-6 kbar and ~600 °C. The different compositions of the hydrating fluid suggest more than one fluid source.  相似文献   

20.
Scapolite and other halogen-rich minerals (phlogopite, amphibole,apatite, titanite and clinohumite) occur in some high-pressureamphibolite facies calc-silicates and orthopyroxene-bearingrocks at Sare Sang (Sar e Sang or Sar-e-Sang), NE Afghanistan.The calc-silicates are subdivided into two groups: garnet-bearingand garnet-free, phlogopite-bearing. Besides garnet and/or phlogopite,the amphibolite facies mineral assemblages in the calc-silicatesinclude clinopyroxene, calcite, quartz and one or more of theminerals scapolite, plagioclase, K-feldspar, titanite, apatiteand rarely olivine. Orthopyroxene-bearing rocks consist of clinopyroxene,garnet, plagioclase, scapolite, amphibole, quartz, calcite andaccessory dolomite and alumosilicate (kyanite?). Retrogradephases in the rocks are plagioclase, scapolite, calcite, amphibole,sodalite, haüyne, lazurite, biotite, apatite and dolomite.The clinopyroxene is mostly diopside and rarely also hedenbergite.Aegirine and omphacite with a maximum jadeite content of 29mol % were also found. Garnet from the calc-silicates is Grs45–95Py0–2and from the orthopyroxene-bearing rocks is Grs10–15Py36–43.Peak P–T metamorphic conditions, calculated using availableexchange thermobarometers and the TWQ program, are 750°Cand 1·3–1·4 GPa. Depending on the rock type,the scapolite exhibits a wide range of composition (from EqAn= 0·07, XCl =0·99 to EqAn = 0·61, XCl =0·07).Equilibria calculated for scapolite and coexisting phases atpeak metamorphic conditions yield XCO2 = 0·03–0·15.XNaCl (fluid), obtained for scapolite, ranges between 0·04and 0·99. Partitioning of F and Cl between coexistingphases was calculated for apatite–biotite and amphibole–biotite.Fluorapatite is present in calc-silicates, but orthopyroxene-bearingrocks contain chlorapatite. Cl preferentially partitions intoamphibole with respect to biotite. All these rocks have sufferedvarious degrees of retrogression, which resulted in removalof halogens, CO2 and S. Halogen- and S-bearing minerals formedduring retrogression and metasomatism are fluorapatite, sodalite,amphibole, scapolite, clinohumite, haüyne, pyrite, andlazurite, which either form veins or replace earlier formedphases. KEY WORDS: scapolite; fluid composition; high-pressure; amphibolite facies; Western Hindukush; Afghanistan  相似文献   

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