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1.
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 D1values of the Bantimala eclogites were compared with those of eclogites with reliable P–T  estimates. This comparison suggests that peak pressures of the Bantimala eclogites were P =18–24  kbar at T  =580–640 °C. These results are consistent with the P–T  range calculated using garnet–rutile–epidote–quartz and lawsonite–omphacite–glaucophane–epidote equilibria.  相似文献   

2.
Garnet from a kinzigite, a high-grade gneiss from the central Black Forest (Germany), displays a prominent and regular retrograde diffusion zoning in Fe, Mn and particularly Mg. The Mg diffusion profiles are suitable to derive cooling rates using recent datasets for cation diffusion in garnet. This information, together with textural relationships, thermobarometry and thermochronology, is used to constrain the pressure–temperature–time history of the high-grade gneisses. The garnet–biotite thermometer indicates peak metamorphic temperatures for the garnet cores of 730–810  °C. The temperatures for the outer rims are 600–650  °C. Garnet–Al2SiO5–plagioclase–quartz (GASP) barometry, garnet–rutile–Al2SiO5–ilmenite (GRAIL) and garnet–rutile–ilmenite–plagioclase–quartz (GRIPS) barometry yield pressures from 6–9  kbar. U–Pb ages of monazite of 341±2  Ma date the low- P high- T metamorphism in the central Black Forest. A Rb/Sr biotite–whole rock pair defines a cooling age of 321±2  Ma. The two mineral ages yield a cooling rate of about 15±2  °C Ma−1. The petrologic cooling rates, with particular consideration of the f O2 conditions for modelling retrograde diffusion profiles, agree with the geochronological cooling rate. The oldest sediments overlying the crystalline basement indicate a minimum cooling rate of 10  °C Ma−1.  相似文献   

3.
Diffusion modelling is applied to layered garnet–pyroxene–quartz coronas, formed by a pressure-induced reaction between plagioclase and primary pyroxene in a metabasic granulite. The reconstructed reaction involves some change in composition of reactant minerals. The distribution of minerals between layers is satisfactorily explained by diffusion-controlled reaction with local equilibrium, in which the diffusion coefficient for Al was smaller than those for Fe, Mg and Ca by a factor of approximately four. Diffusion of Mg towards plagioclase implies a chemical-potential gradient for MgO component in a direction opposite to the changing Mg content of garnet; this is explained by the influence of Al2O3 on the chemical potential of the pyrope end-member. Grain-boundary diffusion is suggested to have operated, possibly with composition gradients different from those in the bulk minerals. Chemical-potential differences across the corona are estimated from the variation in garnet composition, enabling affinity (the free energy change driving the reaction) to be estimated as 6.9±1.8  kJ per 24-oxygen mole of garnet produced. This implies that the pressure for equilibrium among the minerals was overstepped by 1.4±0.4  kbar. The probable P–T conditions of reaction were in the range 650–790  °C, 8–10  kbar. Assuming a timescale of reaction between 106 and 108 years, estimated diffusion coefficients for Fe, Mg and Ca are in the range 9×10−23 to 5×10−20 m2 s−1. These are consistent with experimental values in the literature for solid-state diffusion, including grain-boundary diffusion.  相似文献   

4.
A ternary solid solution model for omphacite with the end-members jadeite (NaAlSi2O6), diopside (CaMgSi2O6) and hedenbergite (CaFeSi2O6) 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+H2O±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   

5.
A second natural occurrence of yoderite   总被引：3，自引：0，他引：3  
A second example of yoderite has been discovered in whiteschists from the Southern Chewore Hills of northern Zimbabwe. The mineral is pale green in colour and occurs in an equilibrium assemblage with talc+chlorite+kyanite+dravite+hematite. There is no quartz present. Recalculated microprobe analyses give a structural formula of Mg2Al5.7Fe0.3Si4O18(OH)2, similar to that obtained for the type locality at Mautia Hill, Tanzania, i.e. Mg2Al5.6Fe0.4Si4O18(OH)2. Textural relationships and relative proportions of minerals suggest that the yoderite was formed by reaction between talc, chlorite, kyanite and hematite. Experimental evidence suggests high-water-pressure metamorphic conditions at temperatures exceeding a reaction curve that extends between 13  kbar at 590  °C and 21  kbar at 650  °C. The yoderite-bearing whiteschist is associated with a 1.4  Ga dismembered ophiolite. It is proposed that this yoderite occurrence is associated with a relict subduction/suture zone.  相似文献   

6.
Calc-silicate granulites from the Bolingen Islands, Prydz Bay, East Antarctica, exhibit a sequence of reaction textures that have been used to elucidate their retrograde P–T path. The highest temperature recorded in the calc-silicates is represented by the wollastonite- and scapolite-bearing assemblages which yield at least 760°C at 6 kbar based on experimental results. The calc-silicates have partially re-equilibrated at lower temperatures (down to 450°C) as evidenced by the successive reactions: (1) wollastonite + scapolite + calcite = garnet + CO2, (2) wollastonite + CO2= calcite + quartz, (3) wollastonite + plagioclase = garnet + quartz, (4) scapolite = plagioclase + calcite + quartz, (5) garnet + CO2+ H2O = epidote + calcite + quartz, and (6) clinopyroxene + CO2+ H2O = tremolite + calcite + quartz.
The reaction sequence observed indicates that a CO2 was relatively low in the wollastonite-bearing rocks during peak metamorphic conditions, and may have been further lowered by local infiltration of H2O from the surrounding migmatitic gneisses on cooling. Fluid activities in the Bolingen calc-silicates were probably locally variable during the granulite facies metamorphism, and large-scale CO2 advection did not occur.
A retrograde P–T path, from the sillimanite stability field ( c. 760°C at 6 kbar) into the andalusite stability field ( c. 450°C at <3 kbar), is suggested by the occurrence of secondary andalusite in an adjacent cordierite–sillimanite gneiss in which sillimanite occurs as inclusions in cordierite.  相似文献   

7.
The Cretaceous Abukuma metamorphic terrane consists of the oceanic Gosaisyo Series overthrust onto the terrigenous Takanuki Series. Although the dominant mineralogy defines one of the classic areas of andalusite–sillimanite type progressive metamorphism, there are several lines of evidence suggesting an earlier higher-pressure (up to c . 12  kbar) history of the Takanuki Series and the nearby Gosaisyo Series. These are: (1) the occurrence of rare although widespread relic kyanite in sillimanite+K-feldspar zone-grade pelitic rocks; (2) the high grossular content of garnet interiors (up to c . 30  mol %) overgrown by Ca-poor rims ( c . 2  mol % grossular) in pelitic rocks containing Al2SiO5 minerals (sillimanite±relic kyanite±retrograde andalusite), plagioclase and quartz; (3) the occurrence of rutile as inclusions in garnet in pelitic rocks; and (4) the occurrence of relic corundum+almandine association in silica-poor and Al–Fe-rich rocks. Garnet in the Takanuki Series pelitic rocks commonly shows textural sector zoning and preserves growth zoning despite the high metamorphic grade, suggesting rapid changes in P–T  conditions and a relatively short duration of high-temperature conditions. Combined with radiometric dating, these observations suggest that the Abukuma sillimanite+K-feldspar zone-grade rocks underwent a clockwise P–T  path with very fast (>4  mm  y−1) average burial and exhumation rates.  相似文献   

8.
A combined fluid inclusion and mineral thermobarometric study in groups of synchronous inclusions in quartz within weakly foliated granites from the Chottanagpur Gneissic Complex, India, reveals super dense carbonic (CO2 with minor CH4 and H2O) inclusions and hypersaline (H2O–NaCl ± NaHCO3) inclusions, with halite- and nahcolite daughter phases. This study documents the highest density (1.115 g cm− 3) CO2 fluids ever reported in granites. Fluid isochores, constructed from CO2 (± CH4) and halite-bearing inclusions, coupled with two-feldspar thermometry constrain the minimum P–T at 8 kbar/ 750 °C for fluid entrapment in granites. By contrast, the carbonic inclusions in quartz from granite-hosted metapelite enclaves contain substantial CH4 (up to 30 mol%), and the entrapment pressure ( 4.3 kbar/600 °C) is considerably lower compared to those in the granites. By implication, the sillimanite-free granites were not derived from the metapelitic enclaves, and instead were formed by partial melting of fluid-heterogeneous lower crustal protoliths, with fluid entrapment at magmatic conditions.  相似文献   

9.
The pressure-sensitive equilibrium among anorthite, quartz and the Ca-tschermak component in clinopyroxene (CaAl2SiO6; CaTs), CaAl2SiOCpx6+SiOQtz2=CaAl2Si2OPl8 (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   

10.
In this work, the factors controlling the formation and preservation of high-pressure mineral assemblages in the metamorphosed orthopyroxene-bearing metagranitoids of the Sandmata Complex, Aravalli-Delhi Mobile Belt (ADMB), northwestern India have been modelled. The rocks range in composition from farsundite through quartz mangerite to opdalite, and with varying K2O, Ca/(Ca + Na)rock and FeOtot + MgO contents. A two stage metamorphic evolution has been recorded in these rocks.
An early hydration event stabilized biotite with or without epidote at the expense of magmatic orthopyroxene and plagioclase. Subsequent high-pressure granulite facies metamorphism (∼15 kbar, ∼800 °C) of these hydrated rocks produced two rock types with contrasting mineralogy and textures. In the non-migmatitic metagranitoids, spectacular garnet ± K-feldspar ± quartz corona was formed around reacting biotite, plagioclase, quartz and/or pyroxene. In contrast, biotite ± epidote melting produced migmatites, containing porphyroblastic garnet incongruent solids and leucosomes.
Applying NCKFMASHTO T–M (H2O) and P–T pseudosection modelling techniques, it is demonstrated that the differential response of these magmatic rocks to high-pressure metamorphism is primarily controlled by the scale of initial hydration. Rocks, which were pervasively hydrated, produced garnetiferous migmatites, while for limited hydration, the same metamorphism formed sub-solidus garnet-bearing coronae. Based on the sequence of mineral assemblage evolution and the mineral compositional zoning features in the two metagranitoids, a clockwise metamorphic P–T path is constrained for the high-pressure metamorphic event. The finding has major implications in formulating geodynamic model of crustal amalgamation in the ADMB.  相似文献   

11.
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+H2O 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   

12.
查明煤中矿物质在不同温度和CO2分压条件下溶解度变化规律,能为注入CO2过程中煤储层渗透率分析提供重要依据。借助水文地球化学模拟软件PHREEQC对在不同温度和CO2分压条件下煤中各矿物的溶解度进行了水化学模拟,得出不同温度和CO2分压条件下矿物质溶解度的变化规律。结果表明:在无CO2分压时,随着温度的升高各矿物的溶解度增加;当溶液中CO2分压增加到一定程度时,随着温度的升高各矿物的溶解度降低（石英除外）;在温度相同时,随着CO2分压的增加,所有矿物（石英除外）溶解度均增加,方解石的溶解度随着CO2分压的升高呈现出迅速增加的趋势,其他矿物随着CO2分压的升高,溶解度增加的速率较为缓慢。   相似文献   

13.
浙西南八都杂岩早中生代泥质麻粒岩变质作用及构造意义   总被引：1，自引：0，他引：1  
遂昌-大柘泥质麻粒岩出露于华夏地块东北部的浙西南八都杂岩中,该岩石保留了典型的减压反应结构.但其变质演化特点、变质作用时代及构造意义目前尚不明确.通过系统的岩相学、矿物化学和同位素年代学分析,结果表明遂昌-大柘泥质麻粒岩记录了4个阶段的变质矿物组合,其中早期进变质阶段M1的矿物组合为石榴石+黑云母+石英;压力峰期变质阶段M2的矿物组合为石榴石+铝绿泥石+金红石+蓝晶石+刚玉+黑云母+石英±十字石,该矿物组合可能预示着岩石曾经历了超高压变质作用过程;峰期变质阶段M3的矿物组合为石榴石+黑云母+夕线石+石英±钾长石±斜长石±钛铁矿;峰后近等温降压M4-1阶段的矿物组合为石榴石+黑云母+夕线石+堇青石+石英+钛铁矿±尖晶石±斜长石±钾长石;M4-2阶段的矿物组合为石榴石+堇青石+夕线石+斜长石+黑云母+石英±钾长石.相平衡模拟结合传统地质温压计限定其峰期变质阶段的温压条件为T=780~810 ℃、P=8.0~9.2 kbar;峰期后近等温降压的M4-1阶段的温压条件为T=780~860 ℃和P=5.7~6.0 kbar,M4-2阶段的温压条件为T=~700 ℃和P=~4.4 kbar,具有典型的顺时针近等温减压型P-T轨迹特征.LA-ICP-MS U-Pb定年结果表明其麻粒岩相变质作用时代为233.5~238.9 Ma.变质作用历史说明浙西南地体可能卷入了古特提斯洋域内印支-华南-华北板块之间的俯冲-碰撞过程,并经历了早中生代的麻粒岩相变质作用后快速折返至地表.   相似文献   

14.
A compilation of literature data on the Fe-Mg composition of coexisting chlorite and chloritoid from metapelites metamorphosed at various P - T  conditions shows that the logarithm of the Fe-Mg partitioning (ln K D) varies linearly with the inverse of temperature, from about 2.4 at 300  °C to about 1.3 at 600  °C. In contrast, no trend was observed with pressure, and the molar volumes of Mg- and Fe-chlorite end-members suggest that the pressure dependence of ln K D is not significant. Therefore, the chloritoid-chlorite Mg-Fe exchange reaction is a potential thermometer and has been empirically calibrated using the analyses of 112 chloritoid-chlorite pairs from 28 different localities. Temperatures estimated using the Chl-Cld thermometer were checked against independent estimates for 20 samples not involved in the calibration (Beni Mzala window, Morocco), and the results are in fair agreement with independent temperature estimates. However, the analytical uncertainties and errors are too large to obtain reliable temperature estimates for extremely Mg-rich or Fe-rich compositions. The Chl-Cld thermometer is unreliable at XMg-CLD<0.2 and XMg-CLD>0.8 at 700  °C, and XMg-CLD<0.1 and XMg-CLD>0.9 at 300  °C. Using the results of the empirical calibration, we calculated new thermodynamic data for daphnite. Implementing these data, it becomes possible to estimate T  and P conditions of metamorphism for the invariant chlorite-chloritoid-quartz-aluminosilicate assemblage that is widespread in low-grade metapelites. These estimates appear to be relevant only in the stability field of kyanite, whereas the uncertainties on the calculated pressure conditions are very large in the stability field of kaolinite and pyrophyllite.  相似文献   

15.
The Fe2+–Mg distribution coefficients between sapphirine and spinel:
were experimentally determined at pressures of 9–13 kbar and temperatures of 950–1150 °C using a natural ultrahigh-temperature (UHT) granulite with paragenesis of these minerals from the Napier Complex in East Antarctica [XMg = Mg / (Fe + Mg); XFe = Fe / (Fe + Mg)]. A new sapphirine–spinel geothermometer has been obtained as:

We applied the exchange thermometer to UHT or high-grade metamorphic rocks that were reported from various complexes in the world. If the KD values of 2.63–4.34 obtained from low-Cr mineral pairs such as XCrSpr < 0.016 and XCrSpl < 0.047 were substituted into the equation, their temperature conditions would be estimated as 806–1050 °C at 11 kbar. The XCr means Cr / (Al + Cr(+ Fe3+)). These temperatures are reasonable retrograde or near peak metamorphic condition.  相似文献   


16.
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 H2O 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 H2O = 8.54 jadeite + 0.57 glaucophane + 3.09 lawsonite + 5.26 quartz. Metagreywackes of the northern Diablo Range were metamorphosed under conditions of P H2O= 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   

17.
The George Sound Paragneiss (GSP) represents a rare Permo-Triassic unit in Fiordland that occurs as a km-scale pillar to gabbroic and dioritic gneiss of c . 120 Ma Western Fiordland Orthogneiss (WFO). It is distinguished from Palaeozoic paragneiss common in western Fiordland (Deep Cove Gneiss) by SHRIMP and laser-ablation U–Pb ages as young as c . 190 Ma and 176Hf/177Lu >0.2828 for detrital zircon grains. The Mesozoic age of the GSP circumvents common ambiguity in the interpretation of Cretaceous v. Palaeozoic metamorphic assemblages in the Deep Cove Gneiss. A shallowly dipping S1 foliation is preserved in the GSP distal to the WFO, cut by 100 m scale migmatite contact zones. All units preserve a steeply dipping S2 foliation. S1 staurolite and sillimanite inclusions in the cores of metapelitic garnet grains distal to the WFO preserve evidence for prograde conditions of T  <   650 °C and P <  8 kbar. Contact aureole and S2 assemblages include Mg-rich, Ca-poor cores to garnet grains in metapelitic schist that reflect WFO emplacement at ≈760 °C and ≈6.5 kbar. S2 kyanite-bearing matrix assemblages and Ca-enriched garnet rims reflect ≈650 °C and ≈11 kbar. Poorly oriented muscovite–biotite intergrowths and rare paragonite reflect post-S2 high- P retrogression and cooling. Pseudosection modelling in NCKFMASH defines a high- P anti-clockwise P–T history for the GSP involving: (i) mid- P amphibolite facies conditions; preceding (ii) thermal metamorphism adjacent to the WFO; followed by (iii) burial to high- P and (iv) high- P cooling induced by tectonic juxtaposition of cooler country rock.  相似文献   

18.
The 'TitaniQ' (Ti-in-quartz) solubility thermometer was applied to migmatitic metapelites from the southern and western Adirondack Highlands, New York, to examine the effect of granulite facies metamorphism on the distribution of Ti in quartz. Both cathodoluminescence imaging and quantitative traverses revealed that individual grains of Adirondack quartz are highly zoned with respect to Ti, and that core-to-rim decreases of Ti are common. Large ranges in calculated temperature were observed within each sample. One sample, not considered to be saturated with respect to TiO2, gave maximum temperatures more than 100 °C lower than previously estimated peak temperatures. Rutile-saturated southern and western Adirondack samples yielded peak estimates of ≥803 ± 11 °C and ∼860–870 °C, respectively, which are similar to previous estimates from major phase thermometry. Minimum Ti-in-quartz matrix temperatures from rutile-saturated samples are 630 °C, which is interpreted as the closure temperature for Ti diffusion in quartz in these samples. This study demonstrates that Ti-in-quartz thermometry can yield details of rock evolution if the textural setting and reaction history of the quartz is clear, and can yield near-peak metamorphic temperatures in some cases, if care is taken to test for post-peak diffusional resetting.  相似文献   

19.
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–Al2O3–SiO2–H2O. 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   

20.
Abstract Three types of mineral associations are described from calc-silicate granulites from the Eastern Ghats, India, where geothermobarometry in associated rocks suggests extremely high P–T conditions of metamorphism ( c . 9 ± 1 kbar, 950° C). These mineral associations are: (i) calcite + quartz + scapolite + plagioclase, (ii) calcite + scapolite + wollastonite + porphyroblastic garnet + coronal garnet and (iii) calcite + quartz + wollastonite + scapolite + porphyroblastic garnet + coronal garnet, all coexisting with K-feldspar, titanite and clinopyroxene. The first two associations evolved through nearly isobaric cooling retrograde paths, whereas the third evolved through a nearly isothermal decompression path followed by an isobaric cooling retrograde path. Textural and compositional characteristics suggest the following mineral reactions in the calc-silicate granulites: calcite + quartz = wollastonite + CO2, calcite + plagioclase = scapolite, calcite + scapolite + wollastonite = porphyroblastic garnet ± quartz + CO2, CaTs + wollastonite = coronal garnet (association ii) and wollastonite + scapolite = coronal garnet (association iii) + quartz + CO2. Andradite content in garnet was buffered by the redox equilibria wollastonite + hedenbergite + O2= andradite + quartz (association iii) and wollastonite + andradite + CaTs + scapolite = hedenbergite + calcite + grossular + O2 (association ii). The contrasting mineral parageneses have been ascribed to interplay of variables such as X CO2, f O2, f HCl in the fluid, bulk Na content and the nature of the retrograde P–T–X CO2 paths through which the rocks evolved.  相似文献   

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