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1.
A ternary solid solution model for omphacite with the end-members jadeite (NaAlSi2 O6 ), diopside (CaMgSi2 O6 ) and hedenbergite (CaFeSi2 O6 ) was derived from experimental data from the literature. The subregular solution model, fitted by linear programming, is best suited to omphacites with very little aegirine component in common eclogites. Applying this solution model to the calculation of equilibrium phase diagrams of eclogites from the Adula nappe (Central Alps, Switzerland) results in large stability fields for common eclogite assemblages (garnet+omphacite+quartz+H2 O±kyanite). Within this field the compositions of garnet and omphacite show very little variation. A precise determination of the peak-pressure and temperature is not possible. The occurrence of amphibole, overgrowing the peak-pressure assemblage in fresh eclogite, suggests retrograde re-equilibration, still under eclogite facies conditions. The computation of isopleths for garnet and pyroxene end-members allows the estimation of the pressure and temperature conditions of this re-equilibration event (19–21 kbar, c . 700 °C). 相似文献
2.
A reaction producing jadeitic pyroxene in metagreywackes of the northern Diablo Range has been identified on the basis of mineral distribution, isograd patterns and composition of coexisting minerals. The appearance of jadeitic pyroxene (∼Jd80 ) is closely followed by the disappearance of pumpellyite, which indicates that pumpellyite plays a major role in the pyroxene-producing reaction. A new projection from hematite, lawsonite, chlorite, quartz and H2 O on to the NaAlO2 -FeO-MgO ternary confirms the role of pumpellyite in pyroxene production and suggests a reaction of the form: 1.00 pumpellyite + 0.31 chlorite + 8.71 albite + 0.70 hematite + 2.00 H2 O = 8.54 jadeite + 0.57 glaucophane + 3.09 lawsonite + 5.26 quartz. Metagreywackes of the northern Diablo Range were metamorphosed under conditions of P H2 O = P total at 200-300 °C and 7.5-10.0 kbar. Despite the low temperatures attained during metamorphism, the assumption of equilibrium yields results consistent with field observations and phase relations. 相似文献
3.
The water-pressure temperature stability field of yoderite,ideally Mg2Al5.6Fe3 + 0.4Si4O18(OH)2, was determined at highoxygen fugacities by high-pressure bracketing runs on eightpossible breakdown reactions involving the phases chlorite,kyanite, talc, staurolite, pyrope, enstatite, boron-free kornerupine,cordierite, quartz, and invariably an excess of hematite. Yoderitewas found to be stable over the surprisingly large PT rangefrom 6 to 25 kbar water pressure and 590 to 795 C. It is thusa high-pressure mineral covering the upper amphibolite and portionsof the eclogite facies. In the presence of quartz its upperpressure stability is reduced to some 15 kbar, and its uppertemperature stability to 715 C. Two of the yoderite-producingreactions are anomalous as they show dehydration in the directiontowards lower temperatures. Importantly, this is also true forthe reaction kyanite + talc + hematite+H2O=yoderite+quartz whichis responsible for the only yoderite occurrence in nature atMautia Hill, Tanzania. Preliminary thermodynamic calculationsindicate that—owing to this unusual dehydration behavior—thestability field for the assemblage yoderite+quartz disappearsfor water activities lower than 0.5. The rarity of yoderitein natural rocks, which is in contrast to its large PT stabilityfield, must be explained on chemical rather than on physicalgrounds. Yoderite can only occur in whiteschist-type bulk compositionsrich in MgO, Al2O3, SiO2, and containing some iron, but poorin alkalis and CaO. Oxygen fugacities must be unusually highto keep Fe trivalent, and—at least for rocks with excessquartz—the water activity must be high as well. In anenvironment of this kind, yoderite formation in the Mautia Hillwhiteschist may have occurred even at constant total pressureand temperature simply by an influx of hydrous fluid duringthe late stages of metamorphism under amphibolite facies conditions. 相似文献
4.
The solid-solid reaction magnesiocarpholite = sudoite + quartz has been bracketed between 350 and 500°C, 6.3 and 7.8 kbar. Because it is impossible to synthesize end-member sudoite, all experiments were carried out using natural minerals as starting materials. Although mineral compositions were very close to those of the end-members, the effect of the fluorine content in carpholite was significant. Particularly in those experiments where sudoite grows at the expense of carpholite, electron microprobe analysis of the run products shows that a more stable F-rich carpholite crystallizes too, and consumes the fluorine released in solution by the breakdown of the original carpholite.
Our experimental results are combined, through a thermodynamic analysis, with a previous data set and with previous experimental data concerning the relative stability of chlorite, talc and magnesiocarpholite with excess of quartz and water as a function of P–T and AlAl(SiMg)-1 substitutions in phyllosilicates. This allows us to constrain the feasible thermodynamic parameters (H°f , sud; S ° sud) and (H°f,car ; S °car ) for the Mg end-members. Using the partition coefficients calculated from natural parageneses, we have computed a petrogenetic grid for the system FeO–MgO–Al2 O3 –SiO2 –H2 O. It demonstrates that parageneses involving sudoite and carpholite can be used as indicators of P–T conditions, up to 600° C, 8 kbar for sudoite, and at higher pressure for carpholite. 相似文献
Our experimental results are combined, through a thermodynamic analysis, with a previous data set and with previous experimental data concerning the relative stability of chlorite, talc and magnesiocarpholite with excess of quartz and water as a function of P–T and AlAl(SiMg)
5.
In order to better identify the mineral phase which controls the rheology of the transition zone (between 410 and 660 km depth) transmission electron microscopy observations were made on several coexisting spinel-garnet assemblies: alkremite xenolith; pyrope-rich – MgO:1.1Al2 O3 spinel assembly deformed at 1173K, 800 MPa in a Griggs apparatus; (Mg,Fe)3 (Al,Mg,Si)2 Si3 O12 majorite – (Mg,Fe)2 SiO4 spinel assembly synthesized in a laser heated diamond anvil cell. It was found that garnet crystals systematically remain undeformed while spinel crystals are plastically deformed. These results are in accord with the assumption that the rheology of majorite is stronger than the rheology of spinel, in the conditions of the transition zone. 相似文献
6.
Oxygen isotope geothermometers for metamorphic rocks 总被引：10，自引：1，他引：10
A. MATTHEWS 《Journal of Metamorphic Geology》1994,12(3):211-219
The Chicago mineral-carbonate oxygen isotope fractionation curves have been combined with mineral-water fractionation data for jadeite, zoisite and rutile and new data for grossular-water to provide a set of self-consistent mineral-pair calibrations. The A coefficients in the equation 1000 In α= A × 106 T-2 of the new mineral-pair fractionations are
Jadeite Zoisite Grossular Rutile
Quartz 1.69 2.00 3.03 5.02
Jadeite 0.31 1.34 3.33
Zoisite 1.03 3.02
Grossular 1.99
The isotopic fractionation properties of natural pyralspite garnet [(Ca, Fe, Mg, Mn)3 Al2 Si3 O12 ] can be approximated by those of the grossular end-member. Appropriate substitutions also yield coefficients for the solid-solution minerals: sodic pyroxene and epidote, e.g.
Aquartz-sodic pyroxene = 2.75 - 1.06Xjd ,
Aquartz-epidote = 2.00 + 0.75Xps
where XJd and X Ps are the mole fractions of the jadeite and pistacite components, respectively.
The new data set is particularly suitable for the geothermometry of metamorphic rocks. δ18 O data from minerals of the high-pressure metamorphic rocks of the Sesia Zone of Italy and Cyclades Complex of Greece yield well-constrained mean temperatures of 572 and 478 C, respectively. Type III blueschist metabasalts of the Franciscan Formation of California give mean quartz-garnet temperatures of 354 C. 相似文献
Jadeite Zoisite Grossular Rutile
Quartz 1.69 2.00 3.03 5.02
Jadeite 0.31 1.34 3.33
Zoisite 1.03 3.02
Grossular 1.99
The isotopic fractionation properties of natural pyralspite garnet [(Ca, Fe, Mg, Mn)
A
A
where X
The new data set is particularly suitable for the geothermometry of metamorphic rocks. δ
7.
The pressure-sensitive equilibrium among anorthite, quartz and the Ca-tschermak component in clinopyroxene (CaAl2 SiO6 ; CaTs), CaAl2 SiOCpx6+SiOQtz2=CaAl2 Si2 OPl8 (SCAn) ,can be used as a geobarometer in granulites with the proper assemblage, and has been calibrated using mineral composition data from partial melting experiments of natural assemblages and from phase equilibrium experiments on the end-member CMAS system. The experimental data cover the P – T range 4–32 kbar and 900–1400 °C. Linear least-squares regression analysis of the experimental data resulted in the following empirical expressions for pressure in terms of composition and temperature: P = 5.066 [±0.760]+ 1300 [±800] T −ln K 276 [±16] · T [±2.5 kbar]or P = 6.330 [±0.116]−ln K 301 [±9]· T [±1.0 kbar] ,where K = a PlAn a CpxCaTs .The first equation incorporates an enthalpy term, but is less accurate than the second equation, in which the enthalpy of reaction is ignored. Application of these expressions to natural and experimental equilibrium mineral assemblages demonstrates that the empirical barometers are applicable over a wide range of pressures (≥4 kbar), temperatures (≥700 °C) and bulk compositions (Mg#≥32.5). 相似文献
8.
J. A. GRANT 《Journal of Metamorphic Geology》2009,27(8):571-578
Calculated results using thermocalc for melting of pelitic compositions are compared with the results of experimental melting of pelite from Morton Pass, Wyoming, USA. The experiments were carried out at 1, 2 and 3.5 kbar, dominantly at 2 kbar. For experimental charges with ('wet') and without ('dry') added H2 O, the agreement is good. This is true for the compositions without added H2 O, in which liquid first appears with the production of orthopyroxene at ∼800 °C, and for the runs with added H2 O, in which melting begins at ∼700 °C, and continues, with the appearance of orthopyroxene between 780 and 800 °C at 2 kbar. The compositions of melts are also compared: the comparison is generally good, except in the modelling of wet runs below ∼780 °C, where the calculated values for FeO and MgO are about one-tenth of the already low analytical values, and in somewhat low calculated values of Al2 O3 compared to the analytical data. A quantitative model to illustrate melting of pelite at Morton Pass is calculated, giving T – X (H2 O) conditions for the observed sets of natural assemblages, along with the reactions at and near the beginning of melting. 相似文献
9.
H.-J. MASSONNE 《Journal of Metamorphic Geology》1989,7(6):567-581
Experiments up to water pressures of 21 kbar have been undertaken to bracket the reactions chlorite + quartz = talc + kyanite + H2O, chlorite + quartz = talc + cordierite + H2O, and talc + kyanite + quartz = cordierite ± H2O by reversed runs in the system MgO-Al2O3-SiO2-H2O (MASH). These reaction curves intersect at an invariant point (IP1) at PH2O = 6.4 ± 0.2 kbar and a temperature of 624 ± 4°C. The curve of the chlorite + quartz breakdown to talc + kyanite + H2O at water pressures above 6.4 kbar shows a negative dP/dT, with the slope decreasing with rising pressure, whereas the slope of the breakdown curve to talc + cordierite + H2O at water pressures is clearly positive. The composition of the chlorite solid solution reacting with quartz has been estimated to be approximately Mg4.85Al1.15[Al1.15Si2.85O10](OH)8 over the entire pressure range investigated. The composition of the talc solid solution forming by the breakdown of chlorite + quartz appears to be Mg2.94Al0.06[Al0.06Si3.94O10](OH)2 at PH2O = 2kbar. With increasing pressure, the Al content of talc decreases, reaching a value of about 0.06 atoms per formula unit at P,H2O = 21 kbar. As a consequence of the new experimental data, the existing phase topologies of the MASH-system and K2O-MASH-system have been revised. For example, the invariant point IP1 and the univariant reaction curve kyanite + talc + H2O = chlorite + cordierite are stable. For this reason, the development of medium- to high-temperature metamorphic rocks compositionally approximating the MASH-system must be reconsidered. The whiteschists from Sar e Sang, Afghanistan, are treated as an example. The application of the present experimental data to metamorphic rocks of more normal composition requires the examination of the influence of further components. This leads to the conclusion that the introduction of Fe2+ into magnesian chlorite extends its stability field in the presence of quartz by 10°-15°C in comparison with pure Mg-chlorite. 相似文献
10.
Ultra-high-pressure (UHP) marble and eclogite in the Su-Lu UHP terrane, eastern China 总被引：22，自引：0，他引：22
A large mass of dolomitic marble including many eclogite blocks occurs in orthogneisses of the Rongcheng area of the Su-Lu province, eastern China. The marble consists mainly of dolomite, calcite (formerly aragonite), graphite, forsterite, diopside, talc, tremolite and phlogopite. Aggregates of talc and calcite occur at the boundary between dolomite and diopside. Tremolite is a reaction product between talc and calcite. Eclogite blocks are rimmed by dark green amphibolite. The primary mineral assemblage in the core of eclogite is Na-bearing garnet (up to 0.2 wt% Na2 O), omphacitic pyroxene, clintonite and rutile. Secondary minerals are pargasitic/edenitic amphibole, plagioclase, sodic diopside, chlorite, zoisite and titanite. The peak metamorphic conditions, based on stability of the dolomite+forsterite+aragonite (now calcite)+graphite assemblage, under conditions where tremolite is unstable, are estimated at T =610–660 °C and P =2.5–3.5 GPa (for X CO=0.001). A reaction between dolomite and diopside to form talc under tremolite-unstable conditions indicates a temperature decrease under ultra-high-pressure conditions ( P >2.4 GPa, X CO<0.0013). The formation of secondary tremolite is consistent with a nearly adiabatic pressure decrease post-dating the ultra-high-pressure metamorphism. The temperature decrease under ultra-high-pressure conditions preceding decompression may reflect the underplating of a cold slab, and the rapid decompression probably corresponds to the upwelling stage promoted by the delamination of a downwelling lithospheric root. The P – T conditions of the amphibolitization stage are estimated at <0.9 GPa and <460 °C, and are similar to conditions recorded by the surrounding orthogneisses. 相似文献
11.
The Feiran–Solaf metamorphic complex of Sinai, Egypt, is one of the highest grade metamorphic complexes of a series of basement domes that crop out throughout the Arabian-Nubian Shield. In the Eastern Desert of Egypt these basement domes have been interpreted as metamorphic core complexes exhumed in extensional settings. For the Feiran–Solaf complex an interpretation of the exhumation mechanism is difficult to obtain with structural arguments as all of its margins are obliterated by post-tectonic granites. Here, metamorphic methods are used to investigate its tectonic history and show that the complex was characterized by a single metamorphic cycle experiencing peak metamorphism at ∼700–750 °C and 7–8 kbar and subsequent isothermal decompression to ∼4–5 kbar, followed by near isobaric cooling to 450 °C. Correlation of this metamorphic evolution with the deformation history shows that peak metamorphism occurred prior to the compressive deformation phase D 2 , while the compressive D 2 and D 3 deformation occurred during the near isothermal decompression phase of the P–T loop. We interpret the concurrence of decompression of the P–T path and compression by structural shortening as evidence for the Najd fault system exhuming the complex in an oblique transpressive regime. However, final exhumation from ∼15 km depth must have occurred due to an unrelated mechanism. 相似文献
12.
Abstract A deerite-bearing rock occurs at the boundary between quartzite and metabasites within the 'schistes lustrés'of eastern Corsica. It contains the typomorphic assemblage pyroxene, blue amphibole, hematite and magnetite. Pyroxene shows homogeneous composition close to the aegirine end-member and blue amphibole is zoned from crossite core to riebeckite rim. The bulk chemical analysis of the rock is remarkable by its very high iron content and the presence of an unusually large amount of Zn which is concentrated in both deerite and amphibole. Electron microprobe analyses of the Corsican deerite are compared with those published in the literature; as shown by deerite from the Fransciscan iron formation, the principal substitution for Fe2+ is Mn whereas the amount of substitution for Fe3+ is low. In the system SiO2 -FeO-Fe2 O3 -Al2 O3 -Na2 O-MgO-H2 O the typomorphic paragenesis can be described by an univariant reaction interpreted as the result of a pressure decrease. P-T conditions of metamorphism, previously estimated to be 8 kbar and 300°C, are in good agreement with present knowledge of the deerite stability field. The occurrence of hematite and magnetite in equilibrium permits an estimation of the oxygen fugacity (log f o2 = -29.41 bar). Oxidation conditions are higher than those previously mentioned in the literature for similar assemblages. 相似文献
13.
Magnesian metapelites of probable Archaean age from Forefinger Point, SW Enderby Land, East Antarctica, contain very-high-temperature granulite facies mineral assemblages, which include orthopyroxene (8–9.5 wt% Al2 O3 )–sillimanite ± garnet ± quartz ± K-feldspar, that formed at 10 ± 1.5 kbar and 950 ± 50°C. These assemblages are overprinted by symplectite and corona reaction textures involving sapphirine, orthopyroxene (6–7 wt% Al2 O3 ), cordierite and sometimes spinel at the expense of porphyroblastic garnet or earlier orthopyroxene–sillimanite. These textures mainly pre-date the development of coarse biotite at the expense of initial mesoperthite, and the subsequent formation of orthopyroxene (4–6 wt% Al2 O3 )–cordierite–plagioclase rinds on late biotite.
The early reaction textures indicate a period of near-isothermal decompression at temperatures above 900°C. Decompression from 10 ± 1.5 kbar to 7–8 kbar was succeeded by biotite formation at significantly lower temperatures (800–850°C) and further decompression to 4.5 ± 1 kbar at 700–800°C.
The later parts of this P–T evolution can be ascribed to the overprinting and reworking of the Forefinger Point granulites by the Late-Proterozoic ( c . 1000 Ma) Rayner Complex metamorphism, but the age and timing of the early high-temperature decompression is not known. It is speculated that this initial decompression is of Archaean age and therefore records thinning of the crust of the Napier Complex following crustal thickening by tectonic or magmatic mechanisms and preceding the generally wellpreserved post-deformational near-isobaric cooling history of this terrain. 相似文献
The early reaction textures indicate a period of near-isothermal decompression at temperatures above 900°C. Decompression from 10 ± 1.5 kbar to 7–8 kbar was succeeded by biotite formation at significantly lower temperatures (800–850°C) and further decompression to 4.5 ± 1 kbar at 700–800°C.
The later parts of this P–T evolution can be ascribed to the overprinting and reworking of the Forefinger Point granulites by the Late-Proterozoic ( c . 1000 Ma) Rayner Complex metamorphism, but the age and timing of the early high-temperature decompression is not known. It is speculated that this initial decompression is of Archaean age and therefore records thinning of the crust of the Napier Complex following crustal thickening by tectonic or magmatic mechanisms and preceding the generally wellpreserved post-deformational near-isobaric cooling history of this terrain. 相似文献
14.
A new petrogenetic grid for low-grade metabasites 总被引：7，自引：0，他引：7
Abstract We have used internally-consistent thermodynamic data to present calculated phase equilibria for the system Na2 O-CaO-MgO-Al2 O3 -SiO2 -H2 O (NCMASH), in the range 0–500° C and 0.1–10 kbar, involving the phases anorthite, glaucophane, grossular, heulandite, jadeite, laumontite, lawsonite, paragonite, prehnite, pumpellyite, stilbite, tremolite, wairakite, zoisite with excess albite, clinochlore, quartz and pure water. Average activity terms derived from published mineral chemical data were included for clinochlore, glaucophane, prehnite, pumpellyite, tremolite, and zoisite. The new petrogenetic grid delineates stability fields and parageneses of common index minerals in zeolite, prehniteactinolite, prehnite-pumpellyite, pumpellyite-actinolite, blueschist and greenschist facies metabasites. The stability fields of mineral assemblages containing prehnite, pumpellyite, epidote, actinolite (+ albite + chlorite + quartz) were analysed in some detail, using activity data calculated from five specific samples. For example, the prehnite-actinolite facies covers a P-T field ranging from about 220 to 320° C at pressures below 4.5 kbar. The transition from the prehnite-actinolite and pumpellyite-actinolite to greenschist facies occurs at about 250–300° C at 1–3 kbar and at about 250–350° C at 3–8 kbar. P-T fields of individual facies overlap considerably due to variations in chemical composition. 相似文献
15.
Hydration of eclogite, Pam Peninsula, New Caledonia 总被引：2，自引：0，他引：2
Garnet glaucophanite and greenschist facies assemblages were formed by the recrystallization of barroisite-bearing eclogite facies metabasites in northern New Caledonia. The mineralogical evolution can be modelled by calculated P–T and P–X H2O diagrams for appropriate bulk rock compositions in the model system CaO–Na2 O–FeO–MgO–Al2 O3 –SiO2 –H2 O. The eclogites, having developed in a clockwise P–T path that reached P ≈19 kbar and T ≈590 °C, underwent decompression with the consumption of free H2 O as the volume of hydrous minerals increased. Eclogite is preserved in domains that experienced no fluid influx following the loss of this fluid. Garnet glaucophanite formed at P ≈16 kbar during semi-pervasive fluid influx. Fluid influx, after further isothermal decompression, was focused in shear zones, and resulted in chlorite–albite-bearing greenschist facies mineral assemblages that reflect P ≈9 kbar. 相似文献
16.
The assemblage diaspore+quartz in metamorphic rocks: a petrological, experimental and thermodynamic study 总被引：1，自引：0，他引：1
The upper pressure limit of pyrophyllite is given by the equilibria (i) pyrophyllite=diaspore+quartz and (ii) pyrophyllite=diaspore+coesite. High- P experimental investigations carried out to locate equilibrium (i) yield brackets between 497 °C/24.8 kbar and 535 °C/25.1 kbar, and between 500 °C/23 kbar and 540 °C/23 kbar. Equilibrium (ii) was bracketed at 550 °C between 26.0 and 28.3 kbar. In the experimental P–T range, equilibria (i) and (ii) are metastable with respect to kyanite. A stable P–T grid is calculated using thermodynamic data derived under consideration of the present experimental results. According to these data, the lower pressure limit of the assemblage diaspore+quartz according to equilibrium (i) range from about 12 kbar/300 °C to 20 kbar/430 °C (in the presence of pure water). The upper stability of diaspore+quartz is limited by the reaction diaspore+quartz=kyanite+H2 O at about 450 °C (nearly independent of pressure) and, to higher pressure, by the quartz=coesite transition. Equilibrium (ii) is metastable over the whole P–T range.
Natural occurrences600.S of the diaspore–quartz assemblage in metamorphic rocks in Sulawesi, New Caledonia, Amorgos and the Vanoise are characterized by minerals indicative of high- P such as ferro-magnesiocarpholite, glaucophane, sodic pyroxene and lawsonite. The metamorphic P–T conditions of these rocks are estimated to be in the range 300–400 °C, >8 kbar. These data are compatible with the derived P–T stability field of the diaspore+quartz assemblage. We conclude that, in metamorphic rocks, diaspore+quartz is, as ferrocarpholite, an indicator for unusual low- T /very high- P settings. 相似文献
Natural occurrences600.S of the diaspore–quartz assemblage in metamorphic rocks in Sulawesi, New Caledonia, Amorgos and the Vanoise are characterized by minerals indicative of high- P such as ferro-magnesiocarpholite, glaucophane, sodic pyroxene and lawsonite. The metamorphic P–T conditions of these rocks are estimated to be in the range 300–400 °C, >8 kbar. These data are compatible with the derived P–T stability field of the diaspore+quartz assemblage. We conclude that, in metamorphic rocks, diaspore+quartz is, as ferrocarpholite, an indicator for unusual low- T /very high- P settings. 相似文献
17.
Coarse-grained whiteschist, containing the assemblage: garnet+kyanite+phengite+talc+quartz/coesite, is an abundant constituent of the ultrahigh-pressure metamorphic (UHPM) belt in the Kulet region of the Kokchetav massif of Kazakhstan.
Garnet displays prograde compositional zonation, with decreasing spessartine and increasing pyrope components, from core to rim. Cores were recrystallized at T=380°C (inner) to 580°C (outer) at P<10 kbar (garnet–ilmenite geothermometry, margarite+quartz stability), and mantles at T=720–760°C and PH20=34–36 kbar (coesite+graphite stability, phengite geobarometer, KFMASH system reaction equilibria). Textural evidence indicates that rims grew during decompression and cooling, within the Qtz-stability field.
Silica inclusions (quartz and/or coesite) of various textural types within garnets display a systematic zonal distribution. Cores contain abundant inclusions of euhedral quartz (type 1 inclusions). Inner mantle regions contain inclusions of polycrystalline quartz pseudomorphs after coesite (type 2), with minute dusty micro-inclusions of chlorite, and more rarely, talc and kyanite in their cores; intense radial and concentric fractures are well developed in the garnet. Intermediate mantle regions contain bimineralic inclusions with coesite cores and palisade quartz rims (type 3), which are also surrounded by radial fractures. Subhedral inclusions of pure coesite without quartz overgrowths or radial fractures (type 4) occur in the outer part of the mantle. Garnet rims are silica-inclusion-free.
Type 1 inclusions in garnet cores represent the low-P, low-T precursor stage to UHPM recrystallization, and attest to the persistence of low-P assemblages in the coesite-stability field. Coesites in inclusion types 2, 3, and 4 are interpreted to have sequentially crystallized by net transfer reaction (kyanite+talc=garnet+coesite+H2O), and were sequestered within the garnet with progressively decreasing amounts of intragranular aqueous fluid.
During the retrograde evolution of the rock, all three inclusion types diverged from the host garnet P–T path at the coesite–quartz equilibrium, and followed a trajectory parallel to the equilibrium boundary resulting in inclusion overpressure. Coesite in type 2 inclusions suffered rapid intragranular H2O-catalysed transformation to quartz, and ruptured the host garnet at about 600°C (when inclusion P27 kbar, garnet host P9 kbar). Instantaneous decompression to the host garnet P–T path, passed through the kyanite+talc=chlorite+quartz reaction equilibrium, resulting in the dusty micro-assemblage in inclusion cores. Type 3 inclusions suffered a lower volumetric proportion transformation to quartz at the coesite–quartz equilibrium, and finally underwent rupture and decompression when T<400°C, facilitating coesite preservation. Type 4 coesite inclusions are interpreted to have suffered minimal transformation to quartz and proceeded to surface temperature conditions along or near the coesite–quartz equilibrium boundary. 相似文献
18.
K. MIYAZAKI I. ZULKARNAIN J. SOPAHELUWAKAN & K. WAKITA 《Journal of Metamorphic Geology》1996,14(5):549-563
High-pressure metamorphic rocks exposed in the Bantimala area, c . 40 km north-east of Ujung Pandang, were formed as a Cretaceous subduction complex with fault-bounded slices of melange, chert, basalt, turbidite, shallow-marine sedimentary rocks and ultrabasic rocks. Eclogites, garnet–glaucophane rocks and schists of the Bantimala complex have estimated peak temperatures of T =580–630 °C at 18 kbar and T =590–640 °C at 24 kbar, using the garnet–clinopyroxene geothermometer. The garnet–omphacite–phengite equilibrium is used to estimate pressures. The distribution coefficient K D1 =[( X pyr )3 ( X grs )6 /( X di )6 ]/[(Al/Mg)M2,wm (Al/Si)T2,wm ]3 among omphacite, garnet and phengite is a good index for metamorphic pressures. The K D1
19.
Decompressional coronas and symplectites in granulites of the Musgrave Complex, central Australia 总被引：2，自引：0，他引：2
Abstract In granulite facies metapelitic rocks in the Musgrave Complex, central Australia, reaction between S1 garnet and sillimanite involves the development in S2 of both garnet + cordierite + hercynitic spinel + biotite and hercynitic spinel + cordierite + sillimanite + biotite. The S2 assemblages occur either in coronas and symplectites, mainly around garnet, or, in rocks in which S2 is more strongly developed, as recrystallized assemblages. Ignoring the presence of biotite and ilmenite, the mineral textures can be accounted for qualitatively by a consideration of the model system FeO-MgO-Al2 O3 -SiO2 (FMAS); the textural relationships accord with decompression accompanying the change from S1 to S2. However, since biotite and ilmenite are involved in the assemblages, the parageneses are better accounted for in terms of equilibria in the expanded model system K2 O-FeO-MgO-Al2 O3 -SiO2 -H2 -TiO2 -Fe2 O3 (KFMASHTO), i.e. AFM + TiO2 + Fe2 O3 . The coronas reflect the tectonic unroofing of at least part of the Musgrave Complex from peak S1 conditions of about 8 kbar to S2 conditions of about 4 kbar. 相似文献
20.
The pyrope-coesite rocks and their country rocks at Parigi,Dora Maira Massif,Western Alps: detailed petrography,mineral chemistry and PT-path 总被引：1，自引：0，他引：1
Both the coarse- and fine-grained varieties of the partly coesite-bearing pyrope-quartzites, their interlayered jadeite-kyanite rocks, and the biotite-phengite gneiss country rock common to all of them were subjected to detailed petrographic and textural studies in order to determine the sequence of crystallisation of their mineral constituents, which were also studied analytically by microprobe. Prior to pyrope and coesite growth, the Mg-rich metapelites were talc-kyanite-chlorite-rutile-ellenbergerite schists which — upon continued prograde metamorphism — developed first pyrope megacrysts in silica-deficient local environments at the expense of chlorite + talc + kyanite, and subsequently the smaller pyrope crystals with coesite inclusions from reacting talc + kyanite. Based on geobarometrically useful mineral inclusions as well as on experimentally determined phase relations, a prograde PT-path — simplified for water activity = 1 — is constructed which passes through the approximate PT-conditions 16 kbar and 560° C, 29 kbar and 720° C, and finally up to 37 kbar at about 800° C, where the Mg-rich metapelite was a pyrope-coesite rock with phengite, kyanite, and talc still present. During the retrograde path, pyrope was altered metasomatically either into phlogopite + kyanite + quartz or, at a later stage, to chlorite + muscovite + quartz. Both assemblages yield PT-constraints, the latter about 7–9 kbar, 500–600° C. The country rock gneisses have also endured high-pressures of at least 15 kbar, but they provide mostly constraints on the lowest portion of the uplift conditions within the greenschist facies (about 5 kbar, 450° C). Microprobe data are presented for the following minerals: pyrope, ellenbergerite, dumortierite (unusually MgTi-rich), jadeite, vermiculite (formed after Na-phlogopite?), paragonite, and for several generations of phengite, chlorite, talc, phlogopite, dravite, and glaucophane in the high-pressure rocks, as well as for biotite, chlorite, phengites, epidote, garnet, albite, and K-feldspar in the country rock gneisses. An outstanding open problem identified in this study is the preservation of minerals as inclusions within kyanite and pyrope beyond their PT-stability limits. 相似文献