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1.
Origin of garnet phenocrysts in calc-alkaline rocks   总被引：2，自引：0，他引：2  
A large number of garnet phenocrysts from Palaeozoic rhyodacites and granodiorite porphyrites from Central and Northeastern Victoria have been analyzed using the electron microprobe. These garnets, from an area of several thousand square miles, are very uniform in composition (dominantly almandine, with subordinate pyrope and minor grossular and spessartine). They show minor zoning with a very thin outer rim slightly richer in almandine and spessartine than the remainder of the phenocryst. They are surrounded by a complex intergrowth of cordierite and hypersthene forming a reaction rim. Resorbed quartz phenocrysts are typically associated with the garnet phenocrysts. The uniform composition, the conspicuous size and the subhedral-euhedral form of the garnet phenocrysts indicate that they crystallized directly from the acid calc-alkaline magma at an early stage of its crystallization. High pressure experimental work on a natural garnet-bearing rhyodacite glass demonstrates that almandine-rich garnet and quartz are near-liquidus phases at 18 and 27 kb , but garnet does not appear until well below the liquidus at 9 kb. A comparison of the composition of the experimentally crystallized garnets with the natural garnets suggests that these acid calc-alkaline magmas began to crystallize at pressures between 9 and 18 kb, i.e. at depths corresponding to the lower crust or upper mantle.  相似文献   

2.
Principal component analysis, using eigenvalues and eigenvectors, of the encountered variation in the chemistry of 153 garnets indicates the following: (1) In low grade metamorphic rocks, spessertite and almandine are distinctly isomorphous. The variability of pyrope content does not influence the binary Fe-Mn relationship. However there may be some influence of the grossularite content. (2) In high grade metamorphic rocks, pyrope and almandine are distinctly isomorphous. Variability of grossularite content does not affect the binary Mg-Fe relationship. However, variability in spessertite content may influence the linearity particularly when there is little pyrope.Similar statistical analysis of the chemical data on 119 samples of clinopyroxenes indicates that only significant changes in the concentrations of Al in octahedral and/or of Al in tetrahedral sites and Ti could cause some change in the FeMg ratio in the mineral.Principal component analysis of the data on coexisting garnet and clinopyroxene could be used to classify rocks into their petrogenetic types.Distribution coefficient calculated by assuming ideal binary solution of Mg and Fe members in pyroxene and garnet is useful to indicate the P-T of the formation of the rocks.  相似文献   

3.
Garnet, an uncommon accessory mineral in igneous rocks, occurs in seven small peraluminous granitoid plutons in the southeastern Arabian Shield; textural equilibrium between garnet and other host granitoid minerals indicates that the garnets crystallized from their host magmas. Compositions of the garnets form three groups that reflect host-granitoid compositions, which in turn reflect source compositions and tectonic regimes in which the host magmas were generated. Garnets from the seven plutons have almandine-rich cores and spessartine-rich rims. This reverse zoning depicts host magma compositional evolution; i.e. rimward spessartine enrichment resulted from progressive, host-magma manganese enrichment. The garnets are heavy rare-earth element enriched; (Lu/La) N ranges from 13 to 355 and one of the garnets contains spectacularly elevated abundances of Y, Ta, Th, U, Zn, Zr, Hf, Sn, and Nb. Involvement of garnets with these trace element characteristics in magma genesis or evolution can have dramatic effects on trace element signatures of the resulting magmas. Other researchers suggest that Mn-enriched magmas are most conducive to garnet nucleation. Although the garnetiferous granitoids discussed here are slightly Mn enriched, other genetically similar peraluminous Arabian granitoids lack garnet; Mn enrichment alone does not guarantee garnet nucleation. The presence of excess alumina in the magma may be a prerequisite for garnet nucleation.  相似文献   

4.
Garnet-bearing mineral assemblages are commonly observed in pelitic schists regionally metamorphosed to upper greenschist and amphibolite facies conditions. Modelling of thermodynamic data for minerals in the system Na2O–K2O–FeO–MgO–Al2O3–SiO2–H2O, however, predicts that garnet should be observed only in rocks of a narrow range of very high Fe/Mg bulk compositions. Traditionally, the nearly ubiquitous presence of garnet in medium- to high-grade pelitic schists is attributed qualitatively to the stabilizing effect of MnO, based on the observed strong partitioning of MnO into garnet relative to other minerals. In order to quantify the dependence of garnet stability on whole-rock MnO content, we have calculated mineral stabilities for pelitic rocks in the system MnO–Na2O–K2O–FeO–MgO–Al2O3–SiO2–H2O for a moderate range of MnO contents from a set of non-linear equations that specify mass balance and chemical equilibrium among minerals and fluid. The model pelitic system includes quartz, muscovite. albite, pyrophyllite, chlorite, chloritoid, biotite, garnet, staurolite, cordierite, andalusite, kyanite. sillimanite, K-feldspar and H2O fluid. In the MnO-free system, garnet is restricted to high Fe/Mg bulk compositions, and commonly observed mineral assemblages such as garnet–chlorite and garnet–kyanite are not predicted at any pressure and temperature. In bulk compositions with XMn= Mn/(Fe + Mg + Mn) > 0.01, however, the predicted garnet-bearing mineral assemblages are the same as the sequence of prograde mineral assemblages typically observed in regional metamorphic terranes. Temperatures predicted for the first appearance of garnet in model pelitic schist are also strongly dependent on whole-rock MnO content. The small MnO contents of normal pelitic schists (XMn= 0.01–0.04) are both sufficient and necessary to account for the observed stability of garnet.  相似文献   

5.
Activity-composition relationships of Ca3Al2Si3O12 (grs) in ternary Ca-Mg-Fe garnets of various compositions have been determined by reversed displaced equilibrium experiments at 1000° C and 900° C and pressures of 8 to 17 kbar. The mixing of grs in garnet is nearly ideal at 30 mol% grs, with positive deviations from ideality at lower grs contents. Models of garnet mixing currently in the literature do not predict this trend. Analysis of the present reversals, in conjunction with a garnet mixing model based solely on calorimetry measurements on the binary joins, indicates that a ternary interaction constant for a ternary asymmetric Margules model (Wohl 1953) cannot be constrained. Apparently, some aspects of the garnet binary joins are still not well-known. An alternative asymmetric empirical model, based on analysis of pseudobinary joins of constant Mg/Mg + Fe(Mg #), reproduces the data well and is able to predict grs activity coefficients for garnets with grs contents between 3 and 40 mol% and Mg numbers between 0 and 0.60. The grossular activity coefficient, grs, is given by:
  相似文献   

6.
In pelitic rocks, under conditions of low f O 2 and low f H 2 O, the stability of the mineral pair cordierite-garnet is limited by five univariant reactions. In sequence from high pressure and low temperature to high temperature and low pressure these are: cordierite+garnet hypersthene+sillimanite+quartz, cordierite+garnet hypersthene+sapphirine+quartz, cordierite+garnet hypersthene+spinel+quartz and cordierite+garnet olivine+spinel +quartz. In this sequence of reactions the Mg/Mg+Fe2+ ratio of all ferro-magnesian minerals involved decreases continuously from the first reaction to the fifth. The five univariant boundaries delimit a wide P-T range over which cordierite and garnet may coexist.Two divariant equilibria in which the Mg/Mg+ Fe2+ ratio of the coexisting phases are uniquely determined by pressure and temperature have been studied in detail. P-T-X grids for the reactions cordierite garnet+sillimanite+quartz and cordierite+hypersthene garnet+quartz are used to obtain pressure-temperature estimates for several high grade metamorphic areas. The results suggest temperatures of formation of 700–850° C and load pressures of 5–10 kb. In rare occasions temperatures of 950–1000° C appear to have been reached during granulite metamorphism.On the basis of melting experiments in pelitic compositions it is suggested that Ca-poor garnet xenocrysts found in calc-alkaline magmas derive from admixed pelitic rocks and did not equilibrate with the calc-alkaline magma.  相似文献   

7.
Three garnet-biotite pairs and eleven garnet-cordierite-biotite triplets from the Steinach aureole (Oberpfalz, North-East Bavaria) were analyzed using an electron probe microanalyzer.The regional metamorphic muscovite-biotite schists contain garnets strongly zoned with Mn-Ca-rich centers and Fe-rich edges, the average composition being almandine 67 — spessartine 4 — pyrope 4 — grossular (+andradite) 25.The first contact garnet that is formed in mica schists of the outermost part of the aureole is small, virtually unzoned, and has an average composition of almandine 52 — spessartine 37 — pyrope 8 — grossular (+andradite) 3. With increasing metamorphic grade, there is a consistent trend to form garnets richer in Fe ending up with a composition almandine 84.5 — spessartine 5.5 — pyrope 7.5 — grossular (+andradite) 2.5. This trend is accompanied by a general increase in grain size and modal amount of garnet. Associated cordierites and biotites also become richer in Fe with increasing grade. While the garnets in the highest grade sillimanite hornfelses are poorly zoned, the transitional andalusite-sillimanite hornfelses contain garnets with distinct but variable zonation profiles.These facts can possibly be explained by the time-temperature relationships in the thermal aureole. In a phase diagram such as the Al-Fe-Mg-Mn tetrahedron, the limiting mineral compositions of a four-phase volume or a three-phase triangle are fixed by T and P (the latter remaining effectively constant within a thermal aureole). Thus, in garnet-cordierite-biotite assemblages, garnet zonation should be controlled by temperature variation rather than by a non-equilibrium depletion process. Taking into account the experimental data of Dahl (1968), a zoned garnet from a transitional andalusite-sillimanite hornfels would reflect a temperature increase of about 40° C during its growth. A hypothetical P-X diagram is proposed to show semi-quantitatively the compositional variation of garnet-cordierite pairs with varying pressures (T constant).  相似文献   

8.
Some inclusions from Salt Lake Crater are essentially single-phase subcalcic clinopyroxenites whose original clinopyroxenes, prior to extensive unmixing, were tschermakitic subcalcic varieties with compositions close to Ca34Mg54Fe12. In addition to copious amounts of orthopyroxene, very minor garnet and spinel also were exsolved from the subcalcic clinopyroxenes.The genesis of the garnet pyroxenite suite at Salt Lake Crater has been examined in terms of three models, namely: (i) cumulates from alkali basaltic magmas; (ii) fractional fusion of basanitic garnet clinopyroxenite; and (iii) anatexis of upper mantle lherzolites. Field, mineralogical, chemical and experimental data collectively favour model (iii) and indicate that the nodules are genetically unrelated to their nephelinitic hosts. The Salt Lake garnet pyroxenites can be closely equated with the garnet pyroxenites in magmatictype layers in certain alpine-type ultramafic massifs and they are also similar to many garnet pyroxenite xenoliths in alkaline volcanics from other localities.Liquids produced by anhydrous partial melting of spinel Iherzolite at pressures of approximately 20 kb commonly have picritic chemistries. The crystallization behaviour of picritic liquids at elevated pressures ( 20 kb) indicates that the initial crystallization products may be either essentially single-phase subcalcic clinopyroxenites (with minimal high pressure fractionation) or a range of olivine-aluminous orthopyroxene-aluminous subcalcic clinopyroxene-garnet-(spinel) assemblages with variable 100 Mg/(Mg+Fe) ratios (when fractionation has been operative). All these assemblages may be subsequently modified by subsolidus exsolution and recrystallization.  相似文献   

9.
Garnet and plagioclase pairs from fourteen selected samples, from garnet to sillimanite zones, collected along a NS traverse throughout the metamorphic basement of NE Sardinia, have been analyzed by microprobe.Beyond the garnet isograd, plagioclase has albitic composition and the garnet (a Ca-rich almandine) shows Ca/ Ca+Mg+Fe ratios of about 0.35–0.30, fairly constant from core to rim.Towards the North, still in the garnet zone, when on the large albitic core of plagioclase a thin and discontinuous oligoclasic rim (An22–An18) formed, we observe in the garnet edge an abrupt decrease of the Ca/Ca+Mg+Fe ratio (0.27–0.16).In the staurolite and sillimanite zones garnet does not show significant Ca-zoning and it is characterized by low Ca content (Ca/Ca+Mg+Fe<0.1); the coexisting plagioclase has oligoclasic (An16–An27) composition.The chemical data and the microstructural evidence on growth time indicate that the garnet and plagioclase had a strong mutual interference in determining the relative Ca distribution.The most relevant reactions are discussed and, in particular, the antipathetical Ca-zoning, recorded by garnet and plagioclase in the garnet zone, is considered as the evidence of temperature increase during growth of the two minerals. It is also suggested that the sharp variation of Ca content at the garnet edge was controlled by the discontinuous nature of plagioclase solid solution in the peristeritic range.The order of appearance of garnet and oligoclase in the basement of NE Sardinia is also discussed in comparison with other well known metamorphic sequence (Vermont, New Zealand and Dalradian). It is concluded that the different order of appearance is controlled other than the different nature of the calcic phases in the lower grade zones also by the in the fluid phase.  相似文献   

10.
Near-liquidus phase relationships of a spinel lherzolite-bearing olivine melilitite from Tasmania were investigated over a P, T range with varying , , and . At 30 kb under MH-buffered conditions, systematic changes of liquidus phases occur with increasing ( = CO2/CO2 +H2O+olivine melilitite). Olivine is the liquidus phase in the presence of H2O alone and is joined by clinopyroxene at low . Increasing eliminates olivine and clinopyroxene becomes the only liquidus phase. Further addition of CO2 brings garnet+orthopyroxene onto the liquidus together with clinopyroxene, which disappears with even higher CO2. The same systematic changes appear to hold at higher and lower pressures also, only that the phase boundaries are shifted to different . The field with olivine- +clinopyroxene becomes stable to higher with lower pressure and approaches most closely the field with garnet+orthopyroxene+clinopyroxene at about 27 kb, 1160 °C, 0.08 and 0.2 (i.e., 6–7% CO2+ 7–8% H2O). Olivine does not coexist with garnet+orthopyroxene+clinopyroxene under these MH-buffered conditions. Lower oxygen fugacities do not increase the stability of olivine to higher and do not change the phase relationships and liquidus temperatures drastically. Thus, it is inferred that olivine melilitite 2927 originates as a 5% melt (inferred from K2 O and P2O5 content) from a pyrolite source at about 27kb, 1160 dg with about 6–7% CO2 and 7–8% H2O dissolved in the melt. The highly undersaturated character of the melt and the inability to find olivine together with garnet and orthopyroxene on the liquidus (in spite of the close approach of the respective liquidus fields) can be explained by reaction relationships of olivine and clinopyroxene with orthopyroxene, garnet and melt in the presence of CO2.  相似文献   

11.
Moderately manganiferous siliceous pelagites near Meyers Pass, Torlesse Terrane, South Canterbury, New Zealand, have been metamorphosed in the prehnite–pumpellyite facies. A conodont colour index measurement suggests T max in the range 190–300 °C. Porphyroblastic manganaxinite, manganoan pumpellyite, manganoan chlorite and trace spessartine-rich garnet and sphalerite have formed in an extremely fine-grained quartz–albite–berthierine–phengite–titanite groundmass. Porphyroblastic manganaxinite semischists and schists are distinctive rocks in prehnite–pumpellyite to lower-grade greenschist and blueschist facies of New Zealand and Japan. Mn in the manganoan pumpellyites substitutes for Ca in W sites. Total Fe/(Fe+Mg) ratios in chlorite are dependent on oxidation state, being ≤0.22 in red hematitic hemipelagites, and ≥0.61 in low-f O2 grey metapelagites. In the low-f O2 metapelagites, manganoan berthierine with little or no chlorite is inferred in the groundmass and iron-rich chlorite occurs as porphyroblasts and veinlets, whereas in the red rocks, Mg-rich chlorite occurs both in groundmasses and veinlets. Variably high Si in the manganoan chlorites correlates with evidence for contaminant phases. The Mn content of chlorite contributing to garnet growth is dependent on metamorphic grade; incipient spessartine indicates a saturation value of 6–8% MnO in chlorite in low-f O2 rocks at Meyers Pass. Lower MnO contents are recorded for otherwise analogous rocks with increasing metamorphic grade, but at a given grade coexisting chlorite and garnet are richer in Mn where f O2 is high. Manganaxinite and manganoan pumpellyite also contributed to reactions forming grossular–spessartine solid solutions. Formation of garnet in siliceous pelagites is dependent on both Mn and Ca content. The spessartine component increases with grade into the greenschist facies. Partial recrystallization of berthierine to chlorite and the growth of porphyroblastic patches of other minerals was facilitated by brittle fracture and access of fluids to an otherwise impermeable matrix; to this extent the very low-grade metamorphism was episodic.  相似文献   

12.
The garnet-cordierite zone, the highest-grade zone of the Ryoke metamorphic rocks in the Yanai district, SW Japan, is defined by the coexistence of garnet and cordierite in pelitic rocks. Three assemblages in this zone are studied in detail, i.e. spinel + cordierite + biotite, garnet + cordierite + biotite and garnet + biotite, all of which contain quartz, K-feldspar and plagioclase. The Mg/(Fe + Mg) in the coexisting minerals decreases in the following order: cordierite, biotite, garnet and spinel. Two facts described below are inconsistent with the paragenetic relation in the K2OFeOMgOAl2O3SiO2H2O (KFMASH) system in terms of an isophysical variation. First, garnet and biotite in the last assemblage have Mg/(Fe + Mg) higher than those in the second. Second, the first two assemblages are described by the reaction,
while they occur in a single outcrop. The addition of MnO, ZnO and TiO2 to the system can resolve the inconsistencies as follows. The assemblage garnet + biotite can consist of garnet and biotite higher in Mg/(Fe + Mg) than those in garnet + cordierite + biotite as long as they are enriched in spessartine and depleted in Al, respectively. The assemblage garnet + cordierite + biotite becomes stable relative to spinel + cordierite + biotite with increasing spessartine content or decreasing gahnite content and the Ti content of biotite. The constituent minerals of the assemblages, spinel + cordierite + biotite and garnet + cordierite + biotite, preserve several reaction microstructures indicative of prograde reactions,
and
together with retrograde reactions,
and
This suggests that the pressure-temperature path of the rocks includes an isobaric heating and an isobaric or decompressional cooling. The high-grade areas consisting of the K-feldspar-cordierite zone, sillimanite-K-feldspar zone and garnet-cordierite zone have prograde paths involving isobaric heating and show a southwards increase in pressure with a thermal maximum in the middle. These high-grade zones are closely associated with the gneissose granitic rocks, suggesting that the Ryoke metamorphism, one of the typical low-pressure type, is caused by the heat supply from the syn-tectonic granitic rocks that emplaced at the middle level of the crust. Received: 22 August 1997 / Accepted: 11 May 1998  相似文献   

13.
Analyses of major and rare earth elements are presented for co-existing garnet, clinopyroxene, and amphibole from a Kakanui eclogite.New and previously published analyses of garnets suggest a gradual increase of Fe and decrease of Mg from xenocrysts through garnet pyroxene eclogitic rocks to amphibole-rich eclogitic rocks. Clinopyroxenes show a parallel increase in Fe/Mg ratio and an increase in Jadeite component and decrease in Tschermak's component. These data indicate crystallization of garnet and clinopyroxene from an alkali-rich undersaturated magma and are consistent with the concept of eclogite fractionation, but rare earth data allow severe constraints to be placed on this process. The eclogites are considered to be deep-seated crystallization products of nephelinite, but eclogite fractionation is small and cannot account for the association of alkali basalt, basanite and nephelinite.  相似文献   

14.
Compositional dependence of apparent partition coefficient of iron and magnesium between coexisting garnet and clinopyroxene from Mt. Higasiakaisi is studied by means of a multicomponent regular solution model. It is shown that garnet and clinopyroxene solid solutions are positively non-ideal, and the non-ideal parameters according to the symmetric regular solution model are 2.58 kcal and 2.39 kcal, respectively, assuming the equilibration temperature of the mass to be 550° C.Notations a i h activity of component i in phase h - ij interaction parameter of component i and j in a solid solution - i activity coefficient of component i - X i mole fraction of component i - K partition coefficient of Fe and Mg between coexisting garnet and clinopyroxene - K apparent partition coefficient of Fe and Mg between coexisting garnet and clinopyroxene - G 0 difference in free energy of the partition reaction - H 0 difference in enthalpy of the partition reaction - S 0 difference in entropy of the partition reaction - R gas constant - G garnet - Alm almandine component - Py pyrope component - Gr grossular component - Sp spessartine component - CPx clinopyroxene - Hd hedenbergite component - Di diopside component - Jd jadeite component - Ts Tschermac's molecule component Deceased on April 17, 1974.  相似文献   

15.
The Violet Town Volcanics are a 373 Ma old, comagmatic, S-type volcanic sequence mainly comprising crystal-rich intracaldera ignimbrites. Rock types vary from rhyolites to rhyodacites, all containing magmatic cordierite and garnet phenocrysts. Variation in the suite is primarily due to fractionation of early-crystallized quartz, plagioclase and biotite (plus minor accessory phases) in a high-level magma chamber prior to eruption. Early magmatic crystallization occurred at around 4 kb and 850° C with melt water contents between 2.8 and 4 wt.%. This high-temperature, markedly water-undersaturated, restite-poor, granitic magma was generated by partial melting reactions involving biotite breakdown in a dominantly quartzofeldspathic source terrain, leaving a granulite facies residue.Table of Less Common Abbreviations Used Pkb pressure in kilobars - T° C temperature in degrees Celsius - mole fraction of water in the fluid - aH2O activity of water - Bi biotite - Cd cordierite - Gt garnet - Py pyrope - Gr grossular - Alm almandine - Sp spessartine - He hercynite - Ilm ilmenite - Kfs potassium feldspar - Opx orthopyroxene - Pl plagioclase - An anorthite - Q quartz - Sill sillimanite - Ap apatite  相似文献   

16.
Ferric iron in mantle-derived garnets   总被引：4，自引：0，他引：4  
The oxidation state of a mantle assemblage may be defined by heterogeneous reactions between oxygen and iron-bearing minerals. In spinel lherzolites, the presence of Fe3+ in spinel allows use of the assemblage olivine-orthopyroxene-spinel to define f O 2 at fixed T and P. As a first step towards establishing an analogous reaction for garnet lherzolites, garnets from mantle-derived xenoliths from South Africa and the USSR have been analyzed with 57Fe Mössbauer spectroscopy at 298 and 77K to determine Fe3+/Fe2+ and the coordination state of iron. Garnets from South African alkremites (pyrope+Mg-spinel) and eclogites, as well as garnet-spinel and low-temperature garnet lherzolites from both South Afica and the USSR, have Fe3+/Fe<0.07. In contrast, garnets from high-temperature garnet lherzolites from within the Kaapvaal craton of South Africa have Fe3+/Fe>0.10. Ferric iron is octahedrally coordinated, and ferrous iron is present in the dodecahedral site in all samples. The occurrence of significant Fe3+ in these garnets necessitates caution in the use of geothermometers and geobarometers that are applied to mantle samples. For example, the presence of 12% of the Fe as Fe3+ in garnets can increase temperatures calculated from existing Fe/Mg geothermometers by>200°C. The concomitant increase in pressures calculated from geobarometers that use the Al content in orthopyroxene coexisting with garnet are 10–15 kbar. Results of calculations based on heterogeneous equilibria between garnet, olivine, and pyroxene are consistent with the derivation of the peridotite samples from source regions that are relatively oxidized, between the f O 2 of the FMQ (quartz-fayalite-magnetite) buffer and that of the WM buffer. No samples yield values of f O 2 as reduced as IW (iron-wüstite buffer).  相似文献   

17.
Garnet, biotite and host rock have been analysed along a traverse from the garnet isograd to the kyanite zone in the Dalradian of Central Perthshire, Scotland. FeO and MgO increase and MnO and CaO decrease in the garnet with increasing grade. Microprobe analyses of the garnets reveal zoning, which indicates that a garnet crystal as a whole does not equilibrate with the matrix during growth. Coexisting biotite varies in composition as a result of the abstraction of MnO, FeO etc. from the rook by the growing garnet, i.e. the mg/mg + fe ratio increases with grade. The microprobe analyses also reveal the size of the system from which garnet abstracted material varied from 0.100 to 2.000 g and the nucleation was frequently instantaneous. It also reveals the equilibrium or non-equilibrium nature of the assemblage, and explains the variation in garnet composition with grade in terms of a segregation model with a changing distribution coefficient. Primary chlorite was analysed from rocks near to the garnet isograd containing garnet and biotite. It has a similar mg/mg + fe value to the coexisting biotite. The results show that the three phase field defining the garnet isograd moves towards the mg corner with increasing grade. The higher grade fields lie to the mg rich side of the three phase field so that the sequence of mineral assemblages across the Barrovian zones in Perthshire, from the garnet isograd to the kyanite zone, can be summarized and displayed on a phase diagram.  相似文献   

18.
Important mineral assemblages of metapelite and quartzite of the Strathgordon area are phengite + chlorite + tourmaline + quartz and phengite + garnet + chlorite + tourmaline + quartz. Over a limited area the Si4+‐content of phengite does not vary significantly and is considered to depend only on the PT regime. The Si4+‐content of phengite coexisting with almandine‐grossular‐spessartine garnet and tourmaline indicate that the maximum metamorphism of the area occurred at 400 ± 50°C and 3 ± 1 kb.  相似文献   

19.
Idioblastic spessartine garnet pervasively developed in Mn-rich rocks and impure manganese carbonate ore at the Lower Proterozoic Nsuta manganese deposit, Western Ghana, contains abundant inclusions of micritic and microconcretionary carbonates and, to a lesser extent, quartz. Detailed mineralogical and microprobe studies indicate all the carbonate phases (i.e. carbonate inclusions in garnet, carbonates coexisting with garnet and carbonates not directly in contact with garnet, the latter hereafter referred to as matrix carbonates) lie within the rhodochrosite-kutnahorite solid solution series, i.e. ~Mn55-80(Ca + Mg)20-45CO3 to Ca42(Mn + Mg)58(CO3)2. Minor compositional differences occur in the various carbonate phases, but partition of major elements among coexisting phases indicate most carbonate minerals strongly fractionate Ca and Mg over coexisting spessartine. The nature, composition and textural relationship of coexisting minerals and inclusions in porphyroblastic spessartine indicate that the latter formed from metamorphic reactions in which rhodochrosite and/or kutnahorite and quartz were consumed, in part corroborating earlier observations on a rhodochrosite precursor for spessartine. Spessartine formation is thus envisaged to have taken place when the predominantly Mn carbonate-quartz assemblage became unstable in the presence of minor amounts of an unknown aluminous phase. Because all the carbonates appear to be low-temperature phases with no indications of significant recrystallisation or homogenisation, it could be argued that the spessartine + rhodochrosite - kutnahorite - quartz - pyrite assemblage stabilised during very low-grade greenschist facies metamorphism under relatively low but uniform fO2 conditions. These observations also suggest the stability field of spessartine could extend to relatively lower temperatures than currently envisaged.  相似文献   

20.
A thermodynamic model is developed that describes the compositional variation of coexisting olivine, orthopyroxene, and ferrite (Fe3O4-MgFe2O4) as a function of and T. The ferrite phase has a cation distribution which varies from nearly inverse to nearly random with increasing T and is described with a model in which the number of sites per formula unit on which mixing occurs varies from 1.67 to 2.0. Given this model and the equilibrium phase composition data for coexisting olivine and ferrite at 1,300° C of Jamieson and Roeder (1984), the ferrite solution is described to an excellent approximation by a symmetric regular solution model with W ft =+14.0 ±0.3 kJ/mole. Orthopyroxene and olivine non-ideality are also considered. The T-dependence of the equilibrium constant for the oxidation reaction 6Fs+2Mt=6Fa+O2 and the two Fe/Mg exchange reactions between olivine-ferrite and olivine-orthopyroxene, are used to calculate the compositional variation of coexisting phases as a function of and T. The results are summarized on an isobaric (1 bar) –1/Tplot with the compositional variation of olivine, ferrite, and orthopyroxene shown by sets of isopleths. The ferrite isopleths intersect those of olivine and orthopyroxene at sufficiently high angles for this assemblage to serve as a sensitive geothermometer and oxygen-barometer. The model is applied to orthopyroxene-ferrite symplectite in coronas around olivine in a metamorphosed gabbro, to olivine-hosted orthopyroxene-ferrite symplectite in unmetamorphosed gabbros and norites and to olivine-hosted orthopyroxene-ferrite symplectites developed within the rims of lherzolite xenoliths.  相似文献   

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