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1.
The zonal structure of prograde garnet in pelitic schists from the medium-grade garnet zone and the higher-grade albite-biotite zone was examined to investigate the evolution of prograde P–T paths of the Sanbagawa metamorphism. The garnet studied shows a bell-shaped chemical zoning of the spessartine component, which decreases in abundance from the core towards the rim. Almandine and pyrope contents and XMg [=Mg/(Mg+Fe2+)] increase monotonously outwards. The general scheme of the zonal structure for grossular content [XGrs=Ca/(Fe2++Mn+Mg+Ca)] can be summarized as: (1) XGrs increases outwards (inner segment) and reaches a maximum at an intermediate position between the crystal core and the rim, then decreases towards the outermost rim (outer segment) (2) the inner segment of garnet in the garnet zone samples tends to have a higher XGrs/XSps values for a given XSps than those in the albite–biotite zone samples (3) average XSps at the maximum XGrs position in the albite–biotite zone samples ranges from 0.02 to 0.12 and is lower than that in the garnet zone samples (0.13–0.32) (4) the maximum XGrs in the albite–biotite zone samples (0.34–0.39 on average) tends to be higher than that in the garnet zone samples (0.26–0.36), and (5) differences of XGrs between the maximum and rim in the albite–biotite zone samples are between 0.10 and 0.14 and higher than those in the garnet zone samples (< 0.11). These facts imply that albite–biotite zone materials (a) were recrystallized under lower dP/dT conditions at an early stage of the prograde metamorphism (b) began their exhumation under higher P–T conditions and (c) have been continuously heated during exhumation for a longer duration than the garnet zone materials. The systematic changes of prograde P–T paths can be interpreted as documenting the evolution of the Sanbagawa subduction zone.  相似文献   

2.
The present study from the Sausar Mobile Belt (SMB) in the southern part of the Central Indian Tectonic zone (CITZ) demonstrates how microdomainal compositional variation of a single garnet porphyroblast in a metapelite granulite sample records the different segments of a near complete P-T path of metamorphic evolution. The microdomainal variation is ascribed to the preservation of growth zoning and heterogeneous distribution of diverse inclusion mineral assemblages. Subsequent mineral reactions under changing P/T conditions were controlled by this compositional heterogeneity. Four stages of metamorphic evolution have been deciphered. An early prograde stage (Mo) is implied by the rare presence of staurolite-biotite-quartz and in places of kyanite inclusion assemblages in other metapelite samples, together with the growth zoning preserved in garnet. The peak metamorphism (M1) at ~9.5 kbar, ~850 °C is consistent with the biotite dehydration melting that produced garnet-K-feldspar and granitic leucosomes. This was followed by near isothermal decompression (M2) at ~6 kbar, ~825 °C, during which different garnet segments behaved as separate microscale bulk compositions and decomposed both internally and externally to produce different retrograde mineral assemblages. In the quartz-bearing domain of almandine-rich and grossular-rich garnet core, grossular components in garnet reacted with included sillimanite and quartz to produce coronal plagioclase (XAn=0.90). By contrast, grossular-rich garnet in quartz-absent domain reacted with included sillimanite to produce layered spinelss {XMg (Mg/Mg+Fe2+) = 0.23–0.26}, XAl (Al/Al+Fe3+)=0.71–0.81}-plagioclase (XAn=0.91)-cordierite {XMg (Mg/Mg+Fe2+) = 0.80–0.83} coronas both in the core and inner rim region of garnet. During post-decompression cooling, reactions occurred at about 600 °C (M3), whereby quartz-bearing, sillimanite-absent microdomains of pyrope-rich, grossular-poor garnet outer rim decomposed to form relatively magnesian assemblages of cordierite-anthophyllite and cordierite-biotite-quartz. M2 spinelss decomposed to polyphase domains of spinel-magnetite±högbomite at this stage. Collating the textural and geothermobarometric results, a clockwise P-T path has been deduced. The deduced P-T loop is consistent with a model of crustal thickening due to continental collision, followed by rapid vertical thinning, which appears to be the general feature of the Sausar Mobile Belt. Using model calculations of the preserved growth and diffusion zoning in garnet, we demonstrate rather short-lived nature of this collision orogeny (in the order of 40–60 Ma).Editorial responsibility: W. Schreyer  相似文献   

3.
Detailed petrographic analysis was performed on samples from five localities within the southern Adirondacks. Textures and zoning patterns in garnet from all samples provide evidence for dehydration melting of biotite. Zoning of grossular in garnet – providing a record of prograde growth – shows both increasing and decreasing trends in garnet from the same sample. However, Ca concentrations at the garnet rims of most samples are identical (grossular = 3.4%). These observations have been interpreted as evidence for the differential timing of garnet nucleation and growth. All Fe/(Fe + Mg) and some spessartine distributions are consistent between samples, displaying diffusive profiles established largely upon cooling. Only one sample, in which retrogression was minimal, contains garnet with flat Fe/(Fe + Mg) profiles. A general pelitic pseudosection constructed in the system MnNCKFMASH reveals a maximum for Ca in garnet where the plagioclase‐out isopleth intersects the solidus (muscovite = 0). The pseudosection predicts bell‐shaped core‐to‐rim profiles of grossular during anatexis, similar to those observed in the rocks. Garnet–biotite thermometry and GASP barometry indicate peak temperatures of at least 790 °C at about 7–9 kbar, similar to conditions determined for the central Adirondacks. Cooling rates determined from finite difference modelling of spessartine and Fe/(Fe + Mg) diffusional profiles indicate a multi‐stage cooling history in which some period of rapid cooling (>200 °C Myr?1) is required.  相似文献   

4.
Published experimental data including garnet and clinopyroxene as run products were used to develop a new formulation of the garnet–clinopyroxene geothermometer based on 333 garnet–clinopyroxene pairs. Only experiments with graphite capsules were selected because of difficulty in estimating the Fe3+ content of clinopyroxene. For the calibration, a published subregular‐solution model was adopted to express the non‐ideality of garnet. The magnitude of the Fe–Mg excess interaction parameter for clinopyroxene (WFeMgCpx), and differences in enthalpy and entropy of the Fe–Mg exchange reaction were regressed from the accumulated experimental data set. As a result, a markedly negative value was obtained for the Fe–Mg excess interaction parameter of clinopyroxene (WFeMgCpx = ? 3843 J mol?1). The pressure correction is simply treated as linear, and the difference in volume of the Fe–Mg exchange reaction was calculated from a published thermodynamic data set and fixed to be ?120.72 (J kbar?1 mol?1). The regressed and obtained thermometer formulation is as follows: where T = temperature, P = pressure (kbar), A = 0.5 Xgrs (Xprp ? Xalm ? Xsps), B = 0.5 Xgrs (Xprp ? Xalm + Xsps), C = 0.5 (Xgrs + Xsps) (Xprp ? Xalm), Xprp = Mg/(Fe2+ + Mn + Mg + Ca)Grt, Xalm = Fe/(Fe2+ + Mn + Mg + Ca)Grt, Xsps = Mn/(Fe2+ + Mn + Mg + Ca)Grt, Xgrs = Ca/(Fe2+ + Mn + Mg + Ca)Grt, XMgCpx = Mg/(Al + Fetotal + Mg)Cpx, XFeCpx = Fe2+/(Al + Fetotal + Mg)Cpx, KD = (Fe2+/Mg)Grt/(Fe2+/Mg)Cpx, Grt = garnet, Cpx = clinopyroxene. A test of this new formulation to the accumulated data gave results that are concordant with the experimental temperatures over the whole range of the experimental temperatures (800–1820 °C), with a standard deviation (1 sigma) of 74 °C. Previous formulations of the thermometer are inconsistent with the accumulated data set; they underestimate temperatures by about 100 °C at >1300 °C and overestimate by 100–200 °C at <1300 °C. In addition, they tend to overestimate temperatures for high‐Ca garnet (Xgrs ≈ 0.30–0.50). This new formulation has been tested against previous formulations of the thermometer by application to natural eclogites. This gave temperatures some 20–100 °C lower than previous formulations.  相似文献   

5.
The Leverburgh Belt and South Harris Igneous Complex in South Harris (northwest Scotland) experienced high-pressure granulite facies metamorphism during the Palaeoproterozoic. The metamorphic history has been determined from the following mineral textures and compositions observed in samples of pelitic, quartzofeldspathic and mafic gneisses, especially in pelitic gneisses from the Leverburgh Belt: (1) some coarse-grained garnet in the pelitic gneiss includes biotite and quartz in the inner core, sillimanite in the outer core, and is overgrown by kyanite at the rims; (2) garnet in the pelitic gneiss shows a progressive increase in grossular content from outer core to rims; (3) the AlVI/AlIV ratio of clinopyroxene from mafic gneiss increases from core to rim; (4) retrograde reaction coronas of cordierite and hercynite+cordierite are formed between garnet and kyanite, and orthopyroxene+cordierite and orthopyroxene+plagioclase reaction coronas develop between garnet and quartz; (5) a P–T path is deduced from inclusion assemblages in garnet and from staurolite breakdown reactions to produce garnet+sillimanite and garnet+sillimanite+hercynite with increasing temperature; and (6) in sheared and foliated rocks, hydrous minerals such as biotite, muscovite and hornblende form a foliation, modifying pre-existing textures. The inferred metamorphic history of the Leverburgh Belt is divided into four stages, as follows: (M1) prograde metamorphism with increasing temperature; (M2) prograde metamorphism with increasing pressure; (M3) retrograde decompressional metamorphism with decreasing pressure and temperature; and (M4) retrograde metamorphism accompanied by shearing. Peak P–T conditions of the M2 stage are 800±30 °C, 13–14 kbar. Pressure increasing from M1 to M2 suggests thrusting of continental crust over the South Harris belt during continent–continent collision. The inferred P–T path and tectonic history of the South Harris belt are different from those of the Lewisian of the mainland.  相似文献   

6.
High-grade metamorphic rocks were used to explore oxygen isotope fractionations between pyroxene and garnet, and to investigate the effects on fractionation factors of the cation substitutions Fe3+Al?1 and Ca(Fe,Mg)?1. Recrystallized, granulite facies (725 °C) wollastonite ores from the northern Adirondack highlands contain essentially only the minerals clinopyroxene (a Di–Hd solid solution)+garnet (a Grs–Adr solid solution)±wollastonite, and exhibit a systematic dependence of measured fractionations on the Fe3+ content of calcic garnet: Δ(Cpx–CaGrt)=(0.14±0.12)+(0.78±0.20)XAdr and Δ(Wo–CaGrt)=(0.15±0.22)+(0.57±0.33)XAdr. In eclogites formed at T ≤650 °C, measured compositions of Ca-poor garnet and omphacite combined with experimental data indicate that Ca-poor, Fe-rich garnet is enriched in 18O compared to both diopside and grossular: extrapolating to 1000 K, Δ(Alm–Di)≈c. 0.2 and Δ(Alm–Grs)≈c. 0.5. Orthopyroxene and clinopyroxene from Gore Mountain, New York, show a constant fractionation that is independent of rock type, as expected if they have the same closure temperature. These data imply Δ(Opx-Cpx)≈c. 0.7 at 1000 K. Measured fractionations among Ca-poor garnet, orthopyroxene, clinopyroxene and hornblende in the Gore Mountain rocks further indicate an 18O enrichment in Ca-poor garnet over Grs (≈c. 0.5 at 1000 K). The new measurements are indistinguishable from expected equilibrium values based on experiments for the minerals enstatite, diopside, grossular, wollastonite and feldspar, but consistently indicate a significant isotope effect for the simple octahedral cation substitutions Fe3+Al?1 (Grs vs. Adr) and Ca(Fe,Mg)?1 (Ca-poor garnet vs. Grs; Opx vs. Cpx). Neither cation substitution has been directly investigated for its effect on 18O/16O fractionation with experiments in silicates. Chemical characterization of minerals is required prior to petrological interpretation of oxygen isotope trends.  相似文献   

7.
Abstract Sapphirine-bearing rocks occur in three conformable, metre-size lenses in intrusive quartzo-feldspathic orthogneisses in the Curaçà valley of the Archaean Caraiba complex of Brazil. In the lenses there are six different sapphirine-bearing rock types, which have the following phases (each containing phlogopite in addition): A: Sapphirine, orthopyroxene; B: Sapphirine, cordierite, orthopyroxene, spinel; C: Sapphirine, cordierite; D: Sapphirine, cordierite, orthopyroxene, quartz; E: Sapphirine, cordierite, orthopyroxene, sillimanite, quartz; F: Sapphirine, cordierite, K-feldspar, quartz. Neither sapphirine and quartz nor orthopyroxene and sillimanite have been found in contact, however. During mylonitization, introduction of silica into the three quartz-free rocks (which represent relict protolith material) gave rise to the three cordierite and quartz-bearing rocks. Stable parageneses in the more magnesian rocks were sapphirine–orthopyroxene and sapphirine–cordierite. In more iron-rich rocks, sapphirine–cordierite, sapphirine-cordierite–sillimanite, cordierite–sillimanite, sapphirine–cordierite–spinel–magnetite and quartz–cordierite–orthopyroxene were stable. The iron oxide content in sapphirine of the six rocks increases from an average of 2.0 to 10.5 wt % (total Fe as FeO) in the order: C,F–A,D–B,E. With increase in Fe there is an increase in recalculated Fe2O3 in sapphirine. The four rock types associated with the sapphirine-bearing lenses are: I: Orthopyroxene, cordierite, biotite, quartz, feldspar tonalitic to grandioritic gneiss; II: Biotite, quartz, feldspar gneiss; III: Orthopyroxene, clinopyroxene, hornblende, plagioclase meta-norite; IV: Biotite, orthopyroxene, quartz, feldspar, garnet, cordierite, sillimanite granulite gneiss. The stable parageneses in type IV are orthopyroxene–cordierite–quartz, garnet–sillimanite–quartz and garnet–cordierite–sillimanite. Geothermobarometry suggests that the associated host rocks equilibrated at 720–750°C and 5.5–6.5 kbar. Petrogenetic grids for the FMASH and FMAFSH (FeO–MgO–Al2O3–Fe2O3–SiO2–H2O) model systems indicate that sapphirine-bearing assemblages without garnet were stabilized by a high Fe3+ content and a high XMg= (Mg/ (Mg+Fe2+)) under these P–T conditions.  相似文献   

8.
Abstract Muscovite-poor pelitic schists in the wallrocks of the Proterozoic Annex sulphide deposit, near Prieska, South Africa, contain peak metamorphic assemblages including Crd + Bt + Sil, St + Sil + Bt, Crd + St + Bt and, rarely, Ky + St ° Crd. All rocks include oligoclase, quartz and commonly Fe–Mn garnet, with or without muscovite. Peak assemblages, assigned to M2 regional metamorphism in the Gordonia Belt (Namaqua Province), are syn- to post-kinematic with respect to the main S2 fabric although larger staurolite grains contain S1 inclusion trails. Garnet–biotite thermometry, utilizing corrections for Fe3+, Mn, AlVI and Ti, yields peak temperatures of 571–624°C at pressures of 4.5–6.0 kbar. Consideration of the sympathetic variation of XMn in garnet with XMg in biotite and the preserved zoning patterns in prograde garnets, together with the inferred prograde transition from kyanite to sillimanite, indicates that heating occurred during mild decompression to the M2 metamorphic peak. Sillimanite and cordierite grew last in the prograde sequence, possibly related to a pulse of thermal metamorphism (M3) that is found along the margin of the Keimoes Suite batholith to the north. Retrograde assemblages, including Ms + Ky + Chl + Qtz (after Crd + Bt), Ky + Ms (after Sil) and Chl + Ms (after St) indicate a period of isobaric cooling (M4a) terminated by rehydration in the kyanite stability field at about 500°C. The size difference between prograde (1–2-mm) and retrograde (0.05–0.1-mm) mineral grains indicates substantial undercooling below equilibrium positions of relevant retrograde reactions prior to rehydration, and explains why cordierite that grew during M2 is almost completely destroyed. Post-M4a regrowth of staurolite and garnet (M4b) is spatially linked to sites of M4a rehydration. It reached temperatures of 510–530°C, remaining within the stability field of kyanite. A best fit of the observed textural history to the Namaqua orogenic cycle involves collision and heating (M2/D2) followed by granite intrusion (M3), rifting (M4a) and renewed heating due to crustal loading during volcanism (M4b). The P–T path for the Annex region is consistent with those derived from elsewhere in the Gordonia Belt and, with modification, to that published already for the nearby Prieska Copper Mines.  相似文献   

9.
Aluminous parageneses containing gedrite, cordierite, garnet, staurolite, biotite, sillimanite, kyanite, quartz or spinel plus corundum are found as dark colored lenses in the polymetamorphic, multideformed Archean complex at Ajitpura in northwest peninsular India. Staurolite, like kyanite, is a relict phase of earlier metamorphism and is excluded as a paragenetic mineral in view of its incompatibility with quartz and gedrite and its lower X Mg values than for garnet of the assemblage. Its stability here is attributed to zinc content of up to 3 wt%. The XMg in other ferromagnesian minerals decreases in the order: cordierite, biotite, gedrite, garnet, as found elsewhere in high grade rocks.The textural criteria and systematic partitioning of Fe and Mg in the ferromagnesian phases, excluding staurolite, indicate attainment of equilibrium during the second metamorphism. From tie line configurations in the phase diagrams, X Mg ratios in the constituent minerals, and other petrographic criteria, it is suggested that gedrite — cordierite-garnet — sillimanite — biotite assemblage has been produced by the reactions: Biotite+Sillimanite+Quartz = Cordierite+Garnet+K-feldspar+Vapor (1) and Biotite+Sillimanite+Quartz = Cordierite +Gedrite+K-feldspar+Vapor (2) which occurred during partial melting of the rocks at fixed P and T conditions.By isothermal P-X(Fe-Mg) sections it has been demonstrated that release of FeO, SiO2 and other components modified the composition of the reactant biotite presumably by the substitution FeSi2 Al, whereby reaction 1 was replaced by reaction 2. Cordierite with higher X Mg was produced with gedrite instead of with garnet, whose X Mg is less than X Mg of gedrite. Reaction 2 has been tentatively located in T-P space from the intersection of some continuous loops in the P-X(Fe-Mg) diagram at 700°C and also by other constraints. The discontinuous reaction 2 is located about 1–2 kilobars higher than reaction 1, which implies that it is difficult to distinguish between effects of pressure and those of melting on the X Mg ratios of the reaction phases.The P-T calibrations of garnet — cordierite, garnet — biotite and garnet — plagioclase equilibria and the calibrations from other dehydration curves give temperatures near 700°C and pressure (assuming ) about 6 kilobars.  相似文献   

10.
In a prograde amphibolite-granulite transition zone in the Namaqualand Metamorphic Complex, metapelites show an interbanding of the amphibolite facies association biotite+sillimanite+quartz with the granulite facies association garnet+cordierite+K-feldspar. Relict graded bedding shows that compositional banding is of sedimentary origin. The garnet-cordierite-K-feldspar gneisses contain quartzofeldspathic segregations surrounding garnets, and have more Fe-rich bulk compositions than the biotite-sillimanite schists.The contrasting asemblages could have formed at the same pressure and temperature provided that a(H2O) was systematically lower in the garnet-cordierite-K-feldspar layers. The a(H2O) reduction resulted from the production of silicate melt by a vapour-absent continuous Fe-Mg reaction such as biotite+sillimanite+quartz=garnet+K-feldspar+liquid which affects Fe-rich compositions before vapour-absent melting occurs in more Mg-rich rocks. The segregations represent the solid and liquid products of the reaction.Such processes imply local control of a(H2O), and indicate that this granulite transition did not result from a regional influx of metasomatising fluids.  相似文献   

11.
An analysis is presented of equilibrium in six specimens ofgarnet—biotite—sillimanite—plagioclase—potashfeldspar—quartz ... gneiss from a metamorphic terrainin south-western Quebec. A nearly uniform Ti content of biotite may be accounted forby an equilibrium (a) involving biotite, sillimanite, quartz,garnet, potash feldspar, and H2O. The nature of the distributionof Fe and Mg between garnet and biotite may be accounted forby another equilibrium (b) involving the same mineral suite,or by a simple exchange equilibrium (c) involving only garnetand biotite. The distribution of Mn between garnet and biotiteis accounted for by an exchange equilibrium (d). A nearly uniformvalue of the ratio Ca content of plagioclase/Ca content of garnetmay be accounted for by an equilibrium (e) involving plagioclase,garnet, sillimanite, and quartz. A proposed equilibrium (f)involving biotite, quartz, ilmenite, potash feldspar, sillimanite,and H2O conflicts with equilibrium (a) and was evidently notestablished in the gneisses. The factors governing the Ca contentof biotite remain largely unknown. Some of these equilibria form potential indicators of relativegeologic temperature, pressure, and chemical potential of H2O.  相似文献   

12.
Textural relations, thermobarometry and petrogenetic grid considerations in the syn-tectonic granitoid massif and the enveloping metasedimentary gneisses at Salur are consistent with a counter-clockwise P–T –t path for the rocks. The low-P/high-T prograde sector is documented by the pre- to syn-D1 cordierite±orthopyroxene±garnet±spinel–bearing metatexite leucosomes in metapelites. Heating and loading of the rocks (syn- to post-D1) resulted in the formation of garnet+orthopyroxene± cordierite-bearing diatexites, and decomposition of cordierite in metatexite leucosomes to orthopyroxene+sillimanite+biotite+quartz symplectites. Near-peak temperature, 850 °C at 8.0 kbar, was reached syn- to post-D2. Post-peak cooling resulted in the stabilization of coronal grossular and anorthite+calcite symplectites at the expense of scapolite+wollastonite+calcite assemblages in calc-silicate gneisses, and the resetting of cation exchange temperatures at 700–750 °C. Near-isothermal decompression at c. 700–750 °C is manifested by the decomposition of garnet porphyroblasts in the granitoid gneisses to plagioclase+orthopyroxene/ilmenite/biotite two-phase coronas and restabilization of cordierite at garnet margins in metapelites. Subsequent low-P, near-isobaric cooling led to the overprinting of granulite facies assemblages by muscovite+calcite assemblages, and further resetting of cation exchange thermometers to lower temperatures c. 600 °C. The tectonothermal evolution of the Salur gneiss complex vis-a-vis the Eastern Ghats Belt is therefore consistent with high degrees of lower crustal melting, followed by prograde heating of the cover rocks due to magma invasion synchronous with crustal compression, and finally thermal relaxation over a protracted period punctuated by tectonic/erosional denudation of the thickened crust.  相似文献   

13.
Manganocummingtonite occurs with spessartine, quartz and pyrolusite in the Chikmara area, Sausar fold belt, central India. Its composition is [Ca0.3–0.35(Mg3.3–3.5Mn1.6–1.8Fe2+ 1.4–1.5)(Si7.931–7.997Aliv 0.003–0.069)O22(OH1.5–2.0F0.0–0.5)] being fairly rich in Ca, which is indicative of metamorphic temperature in the amphibolite facies. The garnet contains 77.5% spessartine, 13% almandine and minor andradite, grossular and pyrope components. Unusually, there is no carbonate, pyroxene, pyroxmangite, rhodonite, magnetite or hematite. The available Al in the rock stabilized garnet and this mineral incorporated minor Fe3+ present in the rock as andradite component. The manganocummingtonite-garnet pairs developed at ～600°C during amphibolite facies metamorphism in low $X_{CO_2 } $ system, stabilized with $X_{Mn/(Mn + Fe^{2 + } + Mg)} $ = 0.25 to 0.28 in the amphibole and 0.85 in the garnet and formed under unusually low fO 2 conditions for the Sausar region, near channelized fluids which deposited quartz may have controlled the fO 2 .  相似文献   

14.
The stability of cordierite and garnet has been studied experimentally in complex, silica oversaturated compositions (in the systems MgO-FeO-Al2O-CaO3-Na2O-K2OSiO2) in which the molecular ratio Al2O3/FeO+MgO<1. Compositions with 100 Mg/Mg+Fe2+ ratios (X) of 0, 30, 50, 70 and 100 have been used to investigate the role of this ratio in determining phase assemblages and P, T coordinates of reactions. The minimum pressure for appearance of garnet at a given temperature is strongly dependent on X total rock.The X-values of co-existing phases (chiefly garnet, cordierite, hypersthene) in divariant equilibrium are a function of temperature and pressure and have been experimentally determined at 900° C, 1000° C and 1100° C. At high temperature (>1050° C) the phases sapphirine and spinel are stable with quartz in Mg-rich and Fe-rich compositions respectively. Experiments in the system MgO-FeO-Al2O3-SiO2 show that for a given X-value and temperature the pressure required to produce Ca-free garnet from hypersthene-cordierite assemblages is 1–2 kb greater than that required to produce garnet containing 6±2 mol percent grossular solid solution in the more complex Ca-bearing system.  相似文献   

15.
Theoretical stability relations have been derived between the phases cordierite (Cd), garnet (Ga), hypersthene (Hy), olivine (Ol), sapphirine (Sa), spinel (Sp), sillimanite (Si) and quartz (Qz) in the system MgO-FeO-Al2O3-SiO2. Natural rock data and experimental evidence suggest that the Mg/Mg+Fe2+ ratio (X) of coexisting ferromagnesian phases decreases as follows: X Cd>X Sa>X Hy>X Ol>X Sp>X Ga. By use of this information four stable invariant points are proposed involving the phases: Cd, Hy, Sa, Ga, Si, Qz; Cd, Sa, Ga, Sp, Si, Qz; Cd, Hy, Sa, Ga, Sp, Qz; Cd, Ga, Hy, Ol, Sp, Qz. All univariant curves in the system are nonterminal, representing the breakdown of a join rather than the stability limit of an individual phase. A detailed treatment of divariant equilibria involving two and three ferromagnesian solid solutions illustrates the potential of these equilibria as Pressure-Temperature indicators. Interactions between solid-solid reactions and dehydration reactions involving biotite in the system MgO-FeO-Al2O3-SiO2-K2O-H2O have been graphically analysed. The addition of biotite to anhydrous divariant assemblages does not affect the composition of coexisting phases at constant P and T but can affect their relative proportions.  相似文献   

16.
In the Boi Massif of Western Timor the Mutis Complex, which is equivalent to the Lolotoi Complex of East Timor, is composed of two lithostratigraphical components: various basement schists and gneisses; and the dismembered remnants of an ophiolite. Cordierite-bearing pelitic schists and gneisses carry an early mineral assemblage of biotite + garnet + plagioclase + Al-silicate, but contain no prograde muscovite; sillimanite occurs in a textural mode which suggests that it replaced and pseudomorphed kyanite at an early stage and some specimens of pelitic schist contain tiny kyanite relics in plagioclase. Textural relations between, and mineral chemistries of, ferro-magnesian phases in these pelitic chists and gneisses suggest that two discontinuous reactions and additional continuous compositional changes have been overstepped, possibly with concomitant anatexis, as a result of decrease in Pload during high temperature metamorphism. The simplified reactions are: garnet and/or biotite + sillimanite + quartz + cordierite + hercynite + ilmenite + excess components. P-T conditions during the development of the early mineral assemblage in the pelitic gneisses are estimated to have been P + 10 kbar and T > 750°C, based upon the plagioclase-garnet-Al-silicate-quartz geobarometer and the garnet-biotite geothermometer. P-T conditions during the subsequent development of cordierite-bearing mineral assemblages in the pelitic gneisses are estimated to have been P + 5 kbar and T + 700°C with XH2O < 0.5, based upon the Fe content of cordierite occurring in the assemblage quartz + plagioclase + sillimanite + biotite + garnet + cordierite coexisting with melt. Final equilibration between some of the phases suggests that conditions dropped to P > 2.3 kbar and T > 600°C. A similar exhumation P-T path is suggested for the pelitic schists with early metamorphic conditions of P > 6.2 kbar and T > 745°C and subsequent development of cordierite under conditions in the range P = 3-4 kbar and T = 600-700°C. The tectonic implications of these P-T estimates are discussed and it is concluded that the P-T path followed by these rocks was caused by decompression during rifting and synmetamorphic ophiolite emplacement resulting from processes during the initiation and development of a convergent plate junction located in Southeast Asia during late Jurassic to Cretaceous time.  相似文献   

17.
Abstract. Pink piemontite-spessartine-bearing and grey-green spessartine-bearing manganiferous quartzose schists derived from siliceous pelagites, and green quartzofeldspathic schists, are described from the greenschist facies of the Haast Schist terrane, near Arrow Junction, western Otago. Electron microprobe data are reported for sphene, spessartine-rich garnet, manganoan epidote, piemontite, tourmaline, phengitic muscovite, chlorite, albite, haematite, rutile, manganoan calcite and chalcopyrite. Metamorphism occurred at about 6.4kbar, 400°C. Xco2 was above the quartz-rutile-calcite-sphene buffer (Xco2± 0.02) throughout the recorded metamorphic history of the piemontite schists. It dropped from above to below this critical buffering value in a spessartine-rich schist and it was close to or below the buffering value in the quartzofeldspathic schists. Production of piemontite required high fO2, believed to be inherited from MnOx in the parent pelagite. Substantial loss of O2 (e.g. minimum of 0.19% by weight in one rock) during diagenesis and/or metamorphism is inferred. In the grey-green schists this inhibited piemontite formation. Slight loss of O2 and Ca2+ accompanied minor late-stage replacement of piemontite by second generation spessartine. Observed zoning and mineral replacements indicate rise of temperature, drop in pressure, or invasion by solutions of lower fO2 and XCO2 equilibrated with surrounding schists. The detailed chemistry of the minerals studied correlates with available Mn and with bulk-rock (Fe3+ x 100)/(Fe2++ Fe3+). The oxidation ratio ranges from 24 in average green quartzofeldspathic schist, through 78 in average grey-green manganiferous quartzose schist, to almost 100 in some piemontite-bearing schists. As Fe2+ gives way to Fe3+, Mg/Fe ratios tend to rise in chlorite, phengite, tourmaline, spessartine, and calcite, Mn increases and Ti decreases in haematite, Mn increases in spessartine and calcite, and Fe increases in rutile. Available divalent cations are depleted relative to Al; chlorite is more aluminous, and phengite more paragonitic than in typical Haast schists.  相似文献   

18.
Summary Garnet occurs as a significant mineral constituent of felsic garnet-biotite granite in the southern edge of the Třebíč pluton. Two textural groups of garnet were recognized on the basis of their shape and relationship to biotite. Group I garnets are 1.5–2.5 mm, euhedral grains which have no reaction relationship with biotite. They are zoned having high XMn at the rims and are considered as magmatic. Group II garnets form grain aggregates up to 2.5 cm in size, with anhedral shape of individual grains. The individual garnet II grains are usually rimmed by biotite and have no compositional zoning. The core of group I garnets and group II garnets contains 67–80 mol% of almandine, 5–19 mol% of pyrope, 7–17 mol% of spessartine and 2–4 mol% of grossular. Biotite occurs in two generations; both are magnesian siderophyllites with Fe/(Fe + Mg) = 0.50–0.69. The matrix biotite in granites (biotite I) has high Ti content (0.09–0.31 apfu) and Fe/(Fe + Mg) ratio between 0.50 and 0.59. Biotite II forms reaction rims around garnet, is poor in Ti (0.00–0.06 apfu) and has a Fe/(Fe + Mg) ratio between 0.61 and 0.69. The textural relationship between biotite and garnet indicates that garnet reacted with granitic melt to form Ti-poor biotite and a new granitic melt, depleted in Ti and Mg and enriched in Fe and Al. In contrast to the host durbachites (hornblende-biotite melagranites), which originated by mixing of crustal melts and upper mantle melts, the origin of garnet-bearing granites is related to partial melting of the aluminium-rich metamorphic series of the Moldanubian Zone.  相似文献   

19.
The cordierite-bearing gneisses occurring as elongate patches in an 8- to 10-km-wide zone along the Achankovil fault-lineament at the northern margin of the southern Kerala crustal segment represent an important lithological unit in the Archaean granulite terrane of south India. The textural relationships in these rocks are consistent with the following main reactions: (1) garnet+quartz=cordierite+hypersthene; (2) garnet+sillimanite+quartz=cordierite; (3) hypersthene+sillimanite+quartz=cordierite; (4) sillimanite+spinel=cordierite+corundum; and (5) biotite+quartz+sillimanite=cordierite+K-feldspar. Many of the mineral associations and reaction textures, including the remarkable preservation of symplectites, are indicative of partial replacement of high-pressure assemblages by cordierite-bearing lower-pressure ones during an event of rapid decompression. Temperature estimates from coexisting mineral phases show 710° (garnet-biotite), 791° (garnet-cordierite) and 788° C (garnet-orthopyroxene). Pressure estimates from mineral assemblages range from 5.4 to 7 kb. Detailed fluid inclusion studies in quartz associated with cordierite show high-density CO2 (0.80–0.95 g/cm3) as the dominant fluid phase, with traces of probable CH4 (?) in the sillimanite-bearing rocks. The isochore for the higher-density fluid inclusions defines a pressure of 5.5 kb. The fracture-bound CO2 and CO2-H2O (±CH4?) inclusions indicate simultaneous entrapment at 400° C and 1.7 kb in the cordierite-hypersthene assemblage and 340° C and 1.2 kb in the cordierite-sillimanite assemblage. The P-T path delineated from combined solid and fluid data corresponds to the piezothermic array of the gneisses and is characterized by T-convex nature, indicative of rapid and virtually isothermal crustal uplift, probably aided by extensional tectonics.  相似文献   

20.
Multiple regression analysis on an extended dataset has been performed to refine the relationship between temperature, pressure, composition and the Fe–Mg distribution between garnet and clinopyroxene. In addition to a significant dependence between the distribution coefficient KD and X GrtCa and X GrtMg#, as shown by the experimental data, the effect of X GrtMn has also been incorporated using data from natural Mn‐rich garnet–clinopyroxene pairs. Multiple regression of data (n=360) covering a large span in pressure, temperature and composition from 27 experimental datasets, combined with 49 natural high‐Mn granulites from Ruby Range, Montana, USA, and Karnataka, India, yields the P–T –compositional relationship (r2=0.98): where KD=(Fe2+/Mg)Grt/(Fe2+/Mg)Cpx, X GrtCa=Ca/(Ca+Mn+Fe2++Mg) in garnet, X GrtMn= Mn/(Ca+Mn+Fe2++Mg) in garnet, and X GrtMg#=Mg/(Mg+Fe2+) in garnet. The Fe2+–Mg equilibrium between garnet and clinopyroxene does not seem to be affected by variations in the sodic content of the co‐existing clinopyroxene in the range X CpxNa=0–0.51. Comparisons between the new and former calibrations of the garnet–clinopyroxene Fe2+–Mg geothermometer clearly demonstrate how the various parameters in each case affect the calculated temperatures. Application of the new expression gives reasonable results for natural garnet–clinopyroxene pairs from various rock types and settings, and should be preferred to previous formulations. Using the new calibration to the self‐consistent dataset of Pattison & Newton (Contributions to Mineralogy and Petrology, 1989, 101, 87–103) suggests a systematic deviation with regard to both temperature and composition between their dataset and the datasets used in the present calibration.  相似文献   

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