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1.
Metasediments in the southern Grossvenediger area (Tauern Window, Austria) were studied along a cross-section through rocks of increasing metamorphic grade from the margin of the Tauern Window in the south to the base of the Upper Schieferhülle, including the Eclogite Zone, in the north. In the southern part of the cross-section there is no evidence for a pre-late Alpine metamorphic history in the form of high-pressure relics or pseudomorphs. Mineral assemblages are characterized by the stability of tremolite + calcite, biotite + calcite and biotite + chlorite + calcite. In the northern part a more complete Alpine metamorphic evolution is preserved. Primary high-pressure assemblages are dolomite + quartz, tremolite + zoisite, zoisite + dolomite + quartz + phengite I and probably tremolite + dolomite + phengite I. Secondary, post-kinematic assemblages [tremolite + calcite, talc + calcite, phengite II + chlorite + calcite (+ quartz), biotite + chlorite + calcite, biotite + zoisite + calcite] formed as a result of the dominant late Alpine metamorphic overprint. The occurrence of biotite + zoisite + calcite is confined to the northernmost area and defines a biotite–zoisite–calcite isograd. P–T estimates based on standard thermobarometric techniques and on stability relationships of tremolite + calcite + dolomite + quartz and zoisite give consistent results. P–T conditions of the main Tertiary metamorphic overprint were 525° C, P= 7.5 ± 1 kbar in the northern part of the cross-section. The southern part was metamorphosed at lower temperatures of 430–470° C. The Si-content of phengites from this area is almost as high as that of phengites from the Eclogite Zone (Simax= 3.4 pfu). Pressures > 10 kbar at 420° C are suggested by phengite barometry according to Massone & Schreyer (1987). In the absence of high-pressure relics or pseudomorphs, these phengites, which lack late Alpine re-equilibration, are the only record that rocks of the southern part probably also experienced an early non-eclogitic high-pressure metamorphism.  相似文献   

2.
A petrological and thermobarometric study of the Lago Teleccio hornfelses was undertaken to reconstruct the polymetamorphic evolution and constrain the P–T conditions of Permian contact metamorphism. The Lago Teleccio metasedimentary rocks record a Variscan regional metamorphism characterized by amphibolite facies mineral assemblages including quartz, plagioclase, K‐feldspar (Kfs 1), biotite, garnet (Grt 1) and staurolite; this was followed by a late‐Variscan mylonitization event. Metamorphism of the Variscan metamorphic rocks at the contact with a Permian granitic intrusion produced static recrystallization and/or new growth of quartz, garnet (Grt 2), plagioclase, K‐feldspar (Kfs 2), cordierite, green spinel, biotite and prismatic sillimanite (Contact 1). This thermal event, which occurred at a peak pressure of 0.23–0.35 GPa, temperature of 670–700 °C and aH2O of 0.75–1, was followed either during post‐contact metamorphism cooling or, more likely, during the early‐Alpine metamorphism by the breakdown of cordierite into an anhydrous kyanite + orthopyroxene + quartz assemblage. The poorly developed early‐Alpine eclogite facies metamorphism (Alpine 1) was characterized by relatively anhydrous mineral associations and low strain, which locally produced coronitic and pseudomorphous microstructures in metasedimentary rocks, with scanty formation of jadeite, zoisite and a new high‐pressure garnet (Grt 3). Greenschist facies retrogression (Alpine 2) was characterized by the local development of a chlorite‐ and muscovite‐bearing mineral association, suggestive of aqueous fluid incursion. In the hornfelses, the limited extent of metamorphic overprinting is suggested by the fine grain size of the Alpine mineral associations, which formed at the expense of the Permian contact metamorphic associations, and was favoured by the anhydrous mineralogy of the hornfelses.  相似文献   

3.
Two types of biotite isograd are defined in the low-grade metamorphism of the Wazuka area, a Ryoke metamorphic terrain in the Kii Peninsula, Japan. The first, BI1, is defined by the reaction of chlorite+K-feldspar= biotite+muscovite+quartz+H2O that took place in psammitic rocks, and the second, BI2, by the continuous reaction between muscovite, chlorite, biotite and quartz in pelitic rocks. The Fe/Mg ratios of the host rocks do not significantly affect the reactions. From the paragenesis of pelitic and psammitic metamorphic rocks, the following mineral zones were established for this low-pressure regional metamorphic terrain: chlorite, transitional, chlorite-biotite, biotite, and sillimanite. The celadonite content of muscovite solid solution in pelitic rocks decreases systematically with the grade of metamorphism from 38% in the chlorite zone to 11% in the biotite zone. Low pressure does not prohibit muscovite from showing the progressive change of composition, if only rocks with appropriate paragenesis are chosen. A qualitative phase diagram of the AKF system relevant to biotite formation suggests that the higher the pressure of metamorphism, the higher the celadonite content of muscovite at BI1, which is confirmed by comparing the muscovites from the Barrovian and Ryoke metamorphism.  相似文献   

4.
Using graphical analysis of the system CaO-Al2O3-SiO2-H2O-CO2, this paper derives a topology relating the minerals calcite, laumontite, wairakite, prehnite, quartz, and zoisite. Simple thermodynamic reasoning allows this system to be applied to natural rocks and indicates that the first appearance of the assemblage epidote-chlorite-quartz (±albite) should mark the upper boundary of zeolite facies. This assemblage forms at the expense of laumontite+prehnite, laumontite+calcite, or laumontite+pumpellyite, with wairakite likely to replace laumontite as the stable zeolite at low pressures. In natural systems this proposed facies boundary is multivariant and, hence, it is likely to be strongly sensitive to compositional variables. For example, Na-bearing wairakite will be more stable than pure Ca-wairakite and increasing abundance of Fe3+ will tend to stabilize epidote+quartz at the expense of the zeolites. Because of this, monitoring the composition of minerals such as epidote, prehnite, or wairakite from lowvariance assemblages may provide a more-sensitive indicator of metamorphic grade than the presence or absence of any particular mineral assemblage.  相似文献   

5.
Mineral assemblages, rock and mineral chemistry, and mineral reactions, in calc-silicate rocks from Koduru area, Andhra Pradesh, India are discussed. Mineralogical and bulk chemical differences indicate 3 calc-silicate rock types — type I with K feldspar+calcite+wollastonite+quartz+scapolite+diopsidess +andraditess+sphene, has relatively high rock oxidation ratios. Type II is a highly calcic variety with high rock MgFe ratios, and has K feldspar+calcite+wollastonite+quartz+scapolite + diopsidess±grossularitess+sphene+zoisite. Type III has K feldspar +calcite+wollastonite+quartz+scapolite+diopsidess +sphene+hornblende+magnetite, and has relatively low oxidation ratio and low MgFe ratio. The 3 calc-silicate rock types have originated as mixtures of limestone/dolomite/marl.Diopside was produced by a reaction involving Ca-amphibole +calcite+quartz, and reversed during retrogression. Andraditess in type I rocks was produced at the expense of hedenbergitic component of pyroxene in a continuous reaction as a consequence of increase in the oxygen content of the original sediment relative to type III. Calcite+quartz reacted to give wollastonite. During cooling an influx of water caused scapolite to alter to zoisite.  相似文献   

6.
The Motuo area is located in the east of the Eastern Himalayan Syntaxis. There outcrops a sequence of high-grade metamorphic rocks, such as metapelites. Petrology and mineralogy data suggest that these rocks have experienced three stages of metamorphism. The prograde metamorphic mineral assemblages(M1) are mineral inclusions(biotite + plagioclase + quartz ± sillimanite ± Fe-Ti oxides) preserved in garnet porphyroblasts, and the peak metamorphic assemblages(M2) are represented by garnet with the lowest XSps values and the lowest XFe# ratios and the matrix minerals(plagioclase + quartz ± Kfeldspar + biotite + muscovite + kyanite ± sillimanite), whereas the retrograde assemblages(M3) are composed of biotite + plagioclase + quartz symplectites rimming the garnet porphyroblasts. Thermobarometric computation shows that the metamorphic conditions are 562–714°C at 7.3–7.4 kbar for the M1 stage, 661–800°C at 9.4–11.6 kbar for the M2 stage, and 579–713°C at 5.5–6.6 kbar for the M3 stage. These rocks are deciphered to have undergone metamorphism characterized by clockwise P-T paths involving nearly isothermal decompression(ITD) segments, which is inferred to be related to the collision of the India and Eurasia plates.  相似文献   

7.
A petrographic and electron microprobe study of an interbedded calc-mica schist from Gassetts, Vermont reveals the complexities of Fe-Mg crystalline solution and gradients in X H2O/X CO2 during regional metamorphism. The common association of microcline+diopside ± zoisite formed from biotite +calcite+quartz may be produced by continuous (Fe-Mg) exchange reactions, despite the implied metastability in the CaO-K2O-MgO-Al2O3-SiO2-H2O-CO2 system. Different assemblages are produced in a reaction zone between carbonate and pelite beds of varying thickness. This illustrates the importance of exhaustion of fluid buffering assemblages due to mineral reactions proceeding on a local scale. Siliceous dolomites at the same metamorphic grade have produced significantly different assemblages to the interlayered carbonatepelite sequence.  相似文献   

8.
The frequency of occurrence of minerals in 1876 samples of Sanbagawa pelitic schist in central Shikoku is summarized on the basis of microscopic observation accompanied, in part, by use of an electron microprobe. All samples contain quartz, plagioclase, phengite, chlorite and graphite. More than 90% of samples contain clinozoisite, titanite and apatite. Garnet is present in 95% of samples from the garnet zone, and biotite is present in 64% of samples from the albite‐biotite zone. Calcite is found in about 40% of samples of the pelitic schist collected from outcrop, but occurs in 95% of the pelitic schist from drill cores. Calcite was apparently ubiquitous in the pelitic schist during the Sanbagawa metamorphism, but must have been dissolved recently by the action of surface or ground water. The mineral assemblages of the Sanbagawa pelitic schist have to be analyzed in the system with excess calcite, quartz, albite (or oligoclase), clinozoisite, graphite and fluid that is composed mainly of H2O, CO2 and CH4. In the presence of calcite, reactions that produce garnet, rutile, oligoclase, biotite and hornblende, some of which define isograds of the metamorphic belt, should be written as mixed volatile equilibria that tend to take place at lower temperature than the dehydration reactions that have been proposed. The presence of calcite in pelitic schist suggests that fluid composition is a variable as important in determining mineral assemblages as pressure and temperature. Thus Ca‐bearing phases must be taken into account to analyze the phase relations of calcite‐bearing pelitic schist, even if CaO content of Sanbagawa pelitic schist is low. As calcite is a common phase, the mineral assemblages of the biotite zone pelitic schist may contravene the mineralogical phase rule and warrant further study.  相似文献   

9.
ABSTRACT The high-grade rocks (metapelite, quartzite, metagabbro) of the Hisøy-Torungen area represent the south-westernmost exposures of granulites in the Proterozoic Bamble sector, south Norway. The area is isoclinally folded and a metamorphic P–T–t path through four successive stages (M1-M4) is recognized. Petrological evidence for a prograde metamorphic event (M1) is obtained from relict staurolite + chlorite + albite, staurolite + hercynite + ilmenite, cordierite + sillimanite, fine-grained felsic material + quartz and hercynite + biotite ± sillimanite within metapelitic garnet. The phase relations are consistent with a pressure of 3.6 ± 0.5 kbar and temperatures up to 750–850°C. M1 is connected to the thermal effect of the gabbroic intrusions prior to the main (M2) Sveconorwegian granulite facies metamorphism. The main M2 granulite facies mineral assemblages (quartz+ plagioclase + K-feldspar + garnet + biotite ± sillimanite) are best preserved in the several-metre-wide Al-rich metapelites, which represent conditions of 5.9–9.1 kbar and 790–884°C. These P–T conditions are consistent with a temperature increase of 80–100°C relative to the adjacent amphibolite facies terranes. No accompanying pressure variations are recorded. Up to 1-mm-wide fine-grained felsic veinlets appear in several units and represent remnants of a former melt formed by the reaction: Bt + Sil + Qtz→Grt + lq. This dehydration reaction, together with the absence of large-scale migmatites in the area, suggests a very reduced water activity in the rocks and XH2O = 0.25 in the C–O–H fluid system was calculated for a metapelitic unit. A low but variable water activity can best explain the presence or absence of fine-grained felsic material representing a former melt in the different granulitic metapelites. The strongly peraluminous composition of the felsic veinlets is due to the reaction: Grt +former melt ± Sil→Crd + Bt ± Qtz + H2O, which has given poorly crystalline cordierite aggregates intergrown with well-crystalline biotite. The cordierite- and biotite-producing reaction constrains a steep first-stage retrograde (relative to M2) uplift path. Decimetre- to metre-wide, strongly banded metapelites (quartz + plagioclase + biotite + garnet ± sillimanite) inter-layered with quartzites are retrograded to (M3) amphibolite facies assemblages. A P–T estimate of 1.7–5.6 kbar, 516–581°C is obtained from geothermobarometry based on rim-rim analyses of garnet–biotite–plagioclase–sillimanite–quartz assemblages, and can be related to the isoclinal folding of the rocks. M4 greenschist facies conditions are most extensively developed in millimetre-wide chlorite-rich, calcite-bearing veins cutting the foliation.  相似文献   

10.
The solid‐state reaction magnesite (MgCO3) + calcite (aragonite) (CaCO3) = dolomite (CaMg(CO3)2) has been identified in metapelites from western Tianshan, China. Petrological studies show that two metamorphic stages are recorded in the metapelites: (1) the peak mineral assemblage of magnesite and calcite pseudomorphs after aragonite which is only preserved as inclusions within dolomite; and (2) the retrograde glaucophane‐chloritoid facies mineral assemblage of glaucophane, chloritoid, dolomite, garnet, paragonite, chlorite and quartz. The peak metamorphic temperatures and pressures are calculated to be 560–600 °C, 4.95–5.07 GPa based on the calcite–dolomite geothermometer and the equilibrium calculation of the reaction dolomite = magnesite + aragonite, respectively. These give direct evidence in UHP metamorphic rocks from Tianshan, China, that carbonate sediments were subducted to greater than 150 km depth. This UHP metamorphism represents a geotherm lower than any previously estimated for subduction metamorphism (< 3.7 °C km?1) and is within what was previously considered a ‘forbidden’ condition within Earth. In terms of the carbon cycle, this demonstrates that carbonate sediments can be subducted to at least 150 km depth without releasing significant CO2 to the overlying mantle wedge.  相似文献   

11.
The Muzkol metamorphic complex in the Central Pamirs contains widespread occurrences of corundum mineralization, sometimes with gem-quality corundum. These occurrences are spatially related to zones of metasomatic alterations in calcite and dolomite marbles and crystalline schists. The calcite marbles contain corundum together with muscovite, scapolite, and biotite; the dolomite marbles contain corundum in association with biotite; and the schists bear this mineral coexisting with biotite and chlorite. All these rocks additionally contain tourmaline, apatite, rutile, and pyrite. The biotite is typically highly aluminous (up to 1.9 f.u. Al), and the scapolite is rich in the marialite end member (60–75 mol %). The crystallization parameters of corundum were estimated using mineral assemblages at T = 600–650°C, P = 4–6 kbar, X CO 2 = 0.2–0.5 at elevated alkalinity of the fluid. The Sr concentration in the calcite and dolomite marbles is low (345–460 and 62–110 ppm, respectively), as is typical of recrystallized sedimentary carbonates. The variations in the 87Sr/86Sr ratio in the calcite and dolomite marbles (0.70852–0.70999 and 0.70902–0.71021, respectively) were controlled by the introduction of radiogenic 87Sr during the metasomatic transformations of the rocks. The isotopic-geochemical characteristics obtained for the rocks and the results of numerical simulations of the fluid-rock interactions indicate that the corundum-bearing metasomatic rocks developed after originally sedimentary Phanerozoic carbonate rocks, with the desilication of the terrigenous material contained in them. This process was a manifestation of regional alkaline metasomatism during the closing stages of Alpine metamorphism. In the course of transformations in the carbonate reservoir, the juvenile fluid flow became undersaturated with respect to silica, which was a necessary prerequisite for the formation of corundum.  相似文献   

12.
Equilibria for several reactions in the system CaO-Al2O3-SiO2-CO2-H2O have been calculated from the reactions calcite+quartz=wollastonite+CO2 (5) and calcite+Al2SiO5+quartz=anorthite+CO2 (19) and other published experimental studies of equilibria in the systems Al2O3-SiO2-H2O and CaO-Al2O3-SiO2-H2O.The calculations indicate that the reactions laumontite+CO2=calcite+kaolinite+2 quartz+2H2O (1) and laumontite+calcite=prehnite+quartz+3H2O+CO2 (3) in the system CaO-Al2O3-SiO2-CO2-H2O, are in equilibrium with an H2O-CO2 fluid phase having -0.0075 for P fluid=P total=2000 bars.These calculations limit the stability of zeolite assemblages to low p CO2.Using the above reactions as model equilibria, several probelms of p CO2 in low grade metamorphism are discussed. (a) the problem of producing zeolitic minerals from metasedimentary assemblages of carbonate, clay mineral, quartz. (b) the significance of calcite (or aragonite) associated with zeolite (or lawsonite) in low grade metamorphism and hydrothermal alteration. (c) the reaction of zeolites (or lawsonite) with calcite (or aragonite) to produce dense Ca-Al-hydrosilicates (eg. prehnite, zoisite, grossular).  相似文献   

13.
At sub‐arc depths, the release of carbon from subducting slab lithologies is mostly controlled by fluid released by devolatilization reactions such as dehydration of antigorite (Atg‐) serpentinite to prograde peridotite. Here we investigate carbonate–silicate rocks hosted in Atg‐serpentinite and prograde chlorite (Chl‐) harzburgite in the Milagrosa and Almirez ultramafic massifs of the palaeo‐subducted Nevado‐Filábride Complex (NFC, Betic Cordillera, S. Spain). These massifs provide a unique opportunity to study the stability of carbonate during subduction metamorphism at P–T conditions before and after the dehydration of Atg‐serpentinite in a warm subduction setting. In the Milagrosa massif, carbonate–silicate rocks occur as lenses of Ti‐clinohumite–diopside–calcite marbles, diopside–dolomite marbles and antigorite–diopside–dolomite rocks hosted in clinopyroxene‐bearing Atg‐serpentinite. In Almirez, carbonate–silicate rocks are hosted in Chl‐harzburgite and show a high‐grade assemblage composed of olivine, Ti‐clinohumite, diopside, chlorite, dolomite, calcite, Cr‐bearing magnetite, pentlandite and rare aragonite inclusions. These NFC carbonate–silicate rocks have variable CaO and CO2 contents at nearly constant Mg/Si ratio and high Ni and Cr contents, indicating that their protoliths were variable mixtures of serpentine and Ca‐carbonate (i.e., ophicarbonates). Thermodynamic modelling shows that the carbonate–silicate rocks attained peak metamorphic conditions similar to those of their host serpentinite (Milagrosa massif; 550–600°C and 1.0–1.4 GPa) and Chl‐harzburgite (Almirez massif; 1.7–1.9 GPa and 680°C). Microstructures, mineral chemistry and phase relations indicate that the hybrid carbonate–silicate bulk rock compositions formed before prograde metamorphism, likely during seawater hydrothermal alteration, and subsequently underwent subduction metamorphism. In the CaO–MgO–SiO2 ternary, these processes resulted in a compositional variability of NFC serpentinite‐hosted carbonate–silicate rocks along the serpentine‐calcite mixing trend, similar to that observed in serpentinite‐hosted carbonate‐rocks in other palaeo‐subducted metamorphic terranes. Thermodynamic modelling using classical models of binary H2O–CO2 fluids shows that the compositional variability along this binary determines the temperature of the main devolatilization reactions, the fluid composition and the mineral assemblages of reaction products during prograde subduction metamorphism. Thermodynamic modelling considering electrolytic fluids reveals that H2O and molecular CO2 are the main fluid species and charged carbon‐bearing species occur only in minor amounts in equilibrium with carbonate–silicate rocks in warm subduction settings. Consequently, accounting for electrolytic fluids at these conditions slightly increases the solubility of carbon in the fluids compared with predictions by classical binary H2O–CO2 fluids, but does not affect the topology of phase relations in serpentinite‐hosted carbonate‐rocks. Phase relations, mineral composition and assemblages of Milagrosa and Almirez (meta)‐serpentinite‐hosted carbonate–silicate rocks are consistent with local equilibrium between an infiltrating fluid and the bulk rock composition and indicate a limited role of infiltration‐driven decarbonation. Our study shows natural evidence for the preservation of carbonates in serpentinite‐hosted carbonate–silicate rocks beyond the Atg‐serpentinite breakdown at sub‐arc depths, demonstrating that carbon can be recycled into the deep mantle.  相似文献   

14.
Calc-silicate rocks occur as elliptical bands and boudins intimately interlayered with eclogites and high-pressure gneisses in the Münchberg gneiss complex of NE Bavaria. Core assemblages of the boudins consist of grossular-rich garnet, diopside, quartz, zoisite, clinozoisite, calcite, rutile and titanite. The polygonal granoblastic texture commonly displays mineral relics and reaction textures such as post kinematic grossular-rich garnet coronas. Reactions between these mineral phases have been modelled in the CaO-Al2O3-SiO2-CO2-H2O system with an internally consistent thermodynamic data base. High-pressure metamorphism in the calc-silicate rocks has been estimated at a minimum pressure of 31 kbar at a temperature of 630d? C with XH2, O ≥ 0.03. Small volumes of a CO2-N2-rich fluid whose composition was buffered on a local scale were present at peak-metamorphic conditions. The P-T conditions for the onset of the amphibolite facies overprint are about 10 kbar at the same temperature. XCo2 of the H2O-rich fluid phase is regarded to have been <0.03 during amphibolite facies conditions. These P-T estimates are interpreted as representing different stages of recrystallization during isothermal decompression. The presence of multiple generations of mineral phases and the preservation of very high-pressure relics in single thin sections preclude pervasive post-peak metamorphic fluid flow as a cause of a re-equilibration within the calc-silicates. The preservation of eclogite facies, very high-pressure relics as well as amphibolite facies reactions textures in the presence of a fluid phase is in agreement with fast, tectonically driven unroofing of these rocks.  相似文献   

15.
In the middle part of the Cévennes, situated at the south-eastern border of the Massif Central, there are outcrops of micaschists, gneisses and granites in which the increase of metamorphic grade was investigated along the river Beaume. This paper presents the results of the petrographic-geochemical analysis of the micaschists of the greenschist facies.Chemical analyses of the micaschist-samples examined petrographically show their nearly constant composition, a fact which e.g., is expressed by similar CaO/Na2O- and MgO/FeO-proportions. As the average values of the determined oxides approach the respective average values of analyses of graywackes recorded by Pettijohn (1957) the original sediment is likely to have been an argillaceous graywacke deficient in calcite.In enrichments of the phyllosilicates pyrophyllite was detected by X-ray diffraction; its amount is about 2 to 5 weight percent of the rocks.With increasing metamorphic grade the following parageneses were found in the metamorphic zones of the greenschist facies: Zone Ia: Quartz+chlorite+pyrophyllite+muscovite+clinozoisite. Zone Ib: Quartz+chlorite+pyrophyllite+muscovite+biotite+clinozoisite.The absence of biotite in Zone Ia, though the chemism of the rocks is practically the same, is obviously due to the different Al2O3-content of the chlorites of Zones Ia and Ib. The chlorite of Zone Ia is more deficient in Al2O3 than the one of Zone Ib. With passage from Zone Ia to Zone Ib the position of the tie line between chlorite and muscovite in the ACF-A'FK-diagram changes in such a way that in Zone Ia, because of purely chemical reasons, biotite cannot occur as coexisting mineral.The beginning of Zone II is characterized by the occurence of almandine, rich in spessartine. The following paragenesis is typical of this zone: Quartz+chlorite+pyrophyllite +muscovite+biotite+almandine+clinozoisite.Additionally the micaschists of these three zones display albite, the greater part of which is concentrated in mm-thin layers with associated minor amounts of quartz and micas. Paragonite whose formation by reaction between albite and pyrophyllite is to be expected based on experimental results (Winkler, 1967, p. 95) could not be proved by X-ray diffraction.In Zone III andalusite occurs instead of pyrophyllite. Furthermore, as chlorite and clinozoisite are absent and oligoclase occurs for the first time this zone is regarded as the first subfacies of the almandine-amphibolite-facies. The chemism and the observed mineral parageneses of the subfacies of the almandine-amphibolite-facies will be treated in a separate publication.  相似文献   

16.
Representative diamond-bearing gneisses and dolomitic marble, eclogite and Ti-clinohumite-bearing garnet peridotite from Unit I at Kumdy Kol and whiteschist from Unit II at Kulet, eastern Kokchetav Massif, northern Kazakhstan, were studied. Diamond-bearing gneisses contain variable assemblages, including Grt+Bt+Qtz±Pl±Kfs±Zo±Chl±Tur±Cal and minor Ap, Rt and Zrn; abundant inclusions of diamond, graphite+chlorite (or calcite), phengite, clinopyroxene, K-feldspar, biotite, rutile, titanite, calcite and zircon occur in garnet. Diamond-bearing dolomitic marbles consist of Dol+Di±Grt+Phl; inclusions of diamond, dolomite±graphite, biotite, and clinopyroxene were identified in garnet. Whiteschists carry the assemblage Ky+Tlc+Grt+Rt; garnet shows compositional zoning, and contains abundant inclusions of talc, kyanite and rutile with minor phlogopite, chlorite, margarite and zoisite. Inclusions and zoning patterns of garnet delineate the prograde P–T path. Inclusions of quartz pseudomorphs after coesite were identified in garnet from both eclogite and gneiss. Other ultrahigh-pressure (UHP) indicators include Na-bearing garnet (up to 0.14 wt% Na2O) with omphacitic Cpx in eclogite, occurrence of high-K diopside (up to 1.56 wt% K2O) and phlogopite in diamond-bearing dolomitic marble, and Cr-bearing kyanite in whiteschist. These UHP rocks exhibit at least three stages of metamorphic recrystallization. The Fe-Mg partitioning between clinopyroxene and garnet yields a peak temperature of 800–1000 °C at P >40 kbar for diamond-bearing rocks, and about 740–780 °C at >28–35 kbar for eclogite, whiteschist and Ti-bearing garnet peridotite. The formation of symplectitic plagioclase+amphibole after clinopyroxene, and replacement of garnet by biotite, amphibole, or plagioclase mark retrograde amphibolite facies recrystallization at 650–680 °C and pressure less than about 10 kbar. The exsolution of calcite from dolomite, and development of matrix chlorite and actinolite imply an even lower grade greenschist facies overprint at c. 420 °C and 2–3 kbar. A clockwise P–T path suggests that supracrustal sediments together with basaltic and ultramafic lenses apparently were subjected to UHP subduction-zone metamorphism within the diamond stability field. Tectonic mixing may have occurred prior to UHP metamorphism at mantle depths. During subsequent exhumation and juxtaposition of many other tectonic units, intense deformation chaotically mixed and mylonitized these lithotectonic assemblages.  相似文献   

17.
Eclogite facies metatroctolites from a variety of Western Alps localities (Voltri, Monviso, Lanzo, Allalin, Zermat–Saas, etc.) that preserve textural evidence of their original form as bimineralic olivine‐plagioclase rocks are considered in terms of calculated mineral equilibria in the system Na2O‐CaO‐FeO‐MgO‐Al2O3‐SiO2‐H2O (NCFMASH). Pseudosections, based on a new petrogenetic grid for NCFMASH presented here, are used to unravel the metamorphic history of the metatroctolites, considering the rocks to consist of different composition microdomains corresponding to the original olivine and plagioclase grains. On the basis that the preservation of the mineral assemblage in each microdomain will tend to be from where on a rock's P–T path the metamorphic fluid phase is used up via rehydration reactions, P–T pseudosections contoured for water content, and P–T path‐MH2O (amount of water) pseudosections, are used to examine fluid behaviour in each microdomain. We show that the different microdomains are likely to preserve their mineral assemblages from different places on the P–T path. For the olivine microdomain, the diagnostic mineral assemblage is chloritoid + talc (+ garnet + omphacite). The preservation of this assemblage, in the light of the closed system P–T path‐MH2O relationships, implies that the microdomain loses its metamorphic fluid as it starts to decompress, and, in the absence of subsequent hydration, the high pressure mineral assemblage is then preserved. In the plagioclase microdomain, the diagnostic assemblage is epidote (or zoisite) + kyanite + quartz suggesting a lower pressure (of about 2 GPa) than for the olivine microdomain. In the light of P–T path‐MH2O relationships, development of this assemblage implies breakdown of lawsonite across the lawsonite breakdown reaction, regardless of the maximum pressure reached. It is likely that the plagioclase microdomain was mainly fluid‐absent prior to lawsonite breakdown, only becoming fluid‐present across the reaction, then immediately becoming fluid‐absent again.  相似文献   

18.
Published phase diagrams for the siliceous carbonate system CaO–MgO–SiO2–CO2–H2O are contradictory because of different estimates of the relative stability of magnesite. Experimental data on magnesite are too ambiguous to determine the validity of these estimates. Therefore, field evidence is used to select the correct phase diagram topology for siliceous carbonate and carbonate ultramafic rocks at pressures of about 2–5 kbar. The primary selection criterion is provided by the existence of the stable assemblage talc+dolomite+forsterite+tremolite+antigorite, which occurs in the Bergell contact aureole and Swiss Central Alps. Field evidence also is used to argue that the reaction magnesite+quartz=enstatite must occur at lower temperature than the reaction dolomite+quartz=diopside. T-X CO 2 and P CO 2-T phase diagrams consistent with these observations are calculated from experimental and thermo-dynamic data. For antigorite ophicarbonate rocks, remarkable agreement is obtained between the spatial distribution of low variance mineral assemblages and the calculated diagrams.  相似文献   

19.
The Huai Kham On gold deposit is located in the central part of the Sukhothai Fold Belt, northern Thailand. The Sukhothai Fold Belt represents an accretionary complex formed by subduction and collision between the Indochina and Sibumasu Terranes. There are many small gold deposits in the Sukhothai Fold Belt; however, the styles and formation environments of those gold deposits are not clear. The geology of the Huai Kham On deposit consists of volcanic and volcanosedimentary rocks, limestone, and low‐grade metamorphic rocks of Carboniferous to Triassic age. Gold‐bearing quartz veins are hosted by volcanic and volcanosedimentary rocks. The quartz veins can be divided into four stages. The mineral assemblage of the gold‐bearing quartz veins of Stages I and II comprises quartz, calcite, illite, pyrite, native gold, galena, chalcopyrite, and sphalerite. Quartz veins of Stage III consist of microcrystalline quartz, dolomite, calcite, pyrite, native gold, and chalcopyrite. Veins of Stage IV consist of calcite, dolomite, chlorite, and quartz. Fluid inclusions in quartz veins are classified into liquid‐rich two‐phase (Types IA and IB), carbonic‐aqueous (Type II), and carbonic (Type III) fluid inclusions. The homogenization temperatures of Types IA and II fluid inclusions that are related to the gold‐bearing quartz veins from Stages I to III ranged from 240° to 280°C. The δ18O values of quartz veins of Stages I to III range from +12.9 to +13.4‰, suggesting the presence of a homogeneous hydrothermal solution without temperature variation such as a decrease of temperature during the formation of gold‐bearing quartz veins from Stages I to III in the Huai Kham On gold deposit. Based on the calculated formation temperature of 280°C, the δ18O values of the hydrothermal solution that formed the gold‐bearing quartz veins range from +3.2 to +3.7‰, which falls into the range of metamorphic waters. The gold‐bearing quartz veins of the Huai Kham On deposit are interpreted to be the products of metamorphic water.  相似文献   

20.
Using the method of Schreinemakers, along with other thermodynamic considerations, a phase diagram for the system CaO-MgO-Al2O3-SiO2-CO2-H2O was constructed. The phases prehnite, pumpellyite, calcite, chlorite, dolomite, quartz, tremolite, talc, zoisite, grossularite and vapor were considered in this construction. The results indicate that prehnite-pumpellyite facies mineral assemblages will only exist in equilibrium with a vapor phase in which the mole fraction of CO2 is less than 0.2 at 1 kb, and less than 0.15 at 2 kb. Although talc could theoretically be a stable phase under these conditions, its common absence from rocks of this facies probably results from the existence of an enantiomorphic point which makes tremolite-calcite-CO2 the stable assemblage at low X CO 2, and the compositionally equivalent talc-calcite-CO2 assemblage stable at moderate X CO 2.  相似文献   

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