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1.
The distribution and textural features of staurolite–Al2SiO5 mineral assemblages do not agree with predictions of current equilibrium phase diagrams. In contrast to abundant examples of Barrovian staurolite–kyanite–sillimanite sequences and Buchan‐type staurolite–andalusite–sillimanite sequences, there are few examples of staurolite–sillimanite sequences with neither kyanite nor andalusite anywhere in the sequence, despite the wide (~2.5 kbar) pressure interval in which they are predicted. Textural features of staurolite–kyanite or staurolite–andalusite mineral assemblages commonly imply no reaction relationship between the two minerals, at odds with the predicted first development (in a prograde sense) of kyanite or andalusite at the expense of staurolite in current phase diagrams. In a number of prograde sequences, the incoming of staurolite and either kyanite, in Barrovian sequences, or andalusite, in Buchan‐type sequences, is coincident or nearly so, rather than kyanite or andalusite developing upgrade of a significant staurolite zone as predicted. The width of zones of coexisting staurolite and either kyanite, in Barrovian sequences, or andalusite, in Buchan‐type sequences, is much wider than predicted in equilibrium phase diagrams, and staurolite commonly persists upgrade until its demise in the sillimanite zone. We argue that disequilibrium processes provide the best explanation for these mismatches. We suggest that kyanite (or andalusite) may develop independently and approximately contemporaneously with staurolite by metastable chlorite‐consuming reactions that occur at lower P–T conditions than the thermodynamically predicted staurolite‐to‐kyanite/andalusite reaction, a process that involves only modest overstepping (<15°C) of the stable chlorite‐to‐staurolite reaction and which is favoured, in the case of kyanite, by advantageous nucleation kinetics. If so, the pressure difference between Barrovian kyanite‐bearing sequences and Buchan andalusite‐bearing sequences could be ~1 kbar or less, in better agreement with the natural record. The unusual width of coexistence of staurolite and Al2SiO5 minerals, in particular kyanite and andalusite, can be accounted for by a combination of lack of thermodynamic driving force for conversion of staurolite to kyanite or andalusite, sluggish dissolution of staurolite, and possibly the absence of a fluid phase to catalyse reaction. This study represents an example of how kinetic controls on metamorphic mineral assemblage development have to be considered in regional as well as contact metamorphism.  相似文献   

2.
Eclogite boudins occur within an orthogneiss sheet enclosed in a Barrovian metapelite‐dominated volcano‐sedimentary sequence within the Velké Vrbno unit, NE Bohemian Massif. A metamorphic and lithological break defines the base of the eclogite‐bearing orthogneiss nappe, with a structurally lower sequence without eclogite exposed in a tectonic window. The typical assemblage of the structurally upper metapelites is garnet–staurolite–kyanite–biotite–plagioclase–muscovite–quartz–ilmenite ± rutile ± silli‐manite and prograde‐zoned garnet includes chloritoid–chlorite–paragonite–margarite, staurolite–chlorite–paragonite–margarite and kyanite–chlorite–rutile. In pseudosection modelling in the system Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O (NCKFMASH) using THERMOCALC, the prograde path crosses the discontinuous reaction chloritoid + margarite = chlorite + garnet + staurolite + paragonite (with muscovite + quartz + H2O) at 9.5 kbar and 570 °C and the metamorphic peak is reached at 11 kbar and 640 °C. Decompression through about 7 kbar is indicated by sillimanite and biotite growing at the expense of garnet. In the tectonic window, the structurally lower metapelites (garnet–staurolite–biotite–muscovite–quartz ± plagioclase ± sillimanite ± kyanite) and amphibolites (garnet–amphibole–plagioclase ± epidote) indicate a metamorphic peak of 10 kbar at 620 °C and 11 kbar and 610–660 °C, respectively, that is consistent with the other metapelites. The eclogites are composed of garnet, omphacite relicts (jadeite = 33%) within plagioclase–clinopyroxene symplectites, epidote and late amphibole–plagioclase domains. Garnet commonly includes rutile–quartz–epidote ± clinopyroxene (jadeite = 43%) ± magnetite ± amphibole and its growth zoning is compatible in the pseudosection with burial under H2O‐undersaturated conditions to 18 kbar and 680 °C. Plagioclase + amphibole replaces garnet within foliated boudin margins and results in the assemblage epidote–amphibole–plagioclase indicating that decompression occurred under decreasing temperature into garnet‐free epidote–amphibolite facies conditions. The prograde path of eclogites and metapelites up to the metamorphic peak cannot be shared, being along different geothermal gradients, of about 11 and 17 °C km?1, respectively, to metamorphic pressure peaks that are 6–7 kbar apart. The eclogite–orthogneiss sheet docked with metapelites at about 11 kbar and 650 °C, and from this depth the exhumation of the pile is shared.  相似文献   

3.
Thermodynamic modelling of metamorphic rocks increases the possibilities of deciphering prograde paths that provide important insights into early orogenic evolution. It is shown that the chloritoid–staurolite transition is not only an indicator of temperature on prograde P–T paths, but also a useful indicator of pressure. The approach is applied to the Moravo‐Silesian eastern external belt of the Bohemian Massif, where metamorphic zones range from biotite to staurolite‐sillimanite. In the staurolite zone, inclusions of chloritoid occur in garnet cores, while staurolite is included at garnet rims and is widespread in the matrix. Chloritoid XFe = 0.91 indicates transition to staurolite at 5 kbar and 550 °C and consequently, an early transient prograde geothermal gradient of 29 °C km?1. The overall elevated thermal evolution is then reflected in the prograde transition of staurolite to sillimanite and in the achievement of peak temperature of 660 °C at a relatively low pressure of 6.5 kbar. To the south and to the west of the studied area, high‐grade metamorphic zones record a prograde path evolution from staurolite to kyanite and development of sillimanite on decompression. Transition of chloritoid to staurolite was reported in two places, with chloritoid XFe = 0.75–0.80, occurring at 8–10 kbar and 560–580 °C, and indicating a transient prograde geothermal gradient of 16–18 °C km?1. These data show variable barric evolutions along strike and across the Moravo‐Silesian domain. Elevated prograde geothermal gradient coincides with areas of Devonian sedimentation and volcanism, and syn‐ to late Carboniferous intrusions. Therefore, we interpret it as a result of heat inherited from Devonian rifting, further fuelled by syntectonic Carboniferous intrusions.  相似文献   

4.
ABSTRACT The Darjeeling-Sikkim region provides a classic example of inverted Himalayan metamorphism. The different parageneses of pelitic rocks containing chlorite, biotite, garnet, staurolite, kyanite, sillimanite, plagioclase and K-feldspar are documented by a variety of textures resulting from continuous and discontinuous reactions in the different zones. Microprobe data of coexisting minerals show that XMg varies in the order: garnet < staurolite < biotite < chlorite. White mica is a solid solution between muscovite and phengite. Garnet is mostly almandine-rich and shows normal growth zoning in the lower part of the Main Central Thrust (MCT) zone, and reverse zoning in the upper part of the zone. Chemographical relations and inferred reactions for different zones are portrayed in AFM space. In the low-grade zones oriented chlorites and micas and rolled garnets grew syntectonically, and were succeeded by cross-cutting chlorites and micas and garnet rims. In the upper zones sillimanite, kyanite and staurolite crystallized during a static inter-kinematic phase. P-T contitions of metamorphism, estimated through different models of geothermobarometry, are estimated to have been 580°c for the garnet zone to a maximum of 770°c for the sillimanite zone. The preferred values of pressure range from 5.0 kbar to 7.7 kbar. Models to explain the inverted metamorphism include overthrusting of a hot high Himalayan slab along a c. 5 km wide ductile MCT zone and the syn- or post-metamorphic folding of isograds.  相似文献   

5.
During prograde metamorphism garnet and, in some higher grade samples, staurolite were produced in a chlorite-chloritoid schist, part of the Precambrian Z to Cambrian Hoosac Formation near Jamaica, VT. Garnet grew during two prograde events separated by a retrogression. This sequence resulted in distinctive inclusion textures and zoning anomalies in garnet produced by diffusive alteration. Textures, reaction space analysis, and mineral compositional variations constrain the possible sequence of reactions in these rocks. Below the staurolite isograd, and to some unknown extent above it, garnet grew by the reaction chloritoid+chlorite+quartz→garnet+H2O. With increasing grade the mineral compositions are displaced towards lower Mn/Fe and higher Mg/Fe ratios. The data are compatible with equilibrium with respect to exchange reactions for the matrix assemblages on a thin section scale and with minerals having closely followed equilibrium paths during reaction. The staurolite isograd coincides with the reaction chloritoid+quartz→garnet+staurolite+chlorite+H2O. This reaction is continuous and trivariant with ZnO becoming an additional component concentrated in staurolite. During this reaction both the Mn/Fe and Mg/Fe ratios of the phases appear to have decreased. This new chemical trend is recorded by garnet zoning profiles and is compatible with trends predicted from phase diagrams. Thus there are two distinct types of garnet zoning reversals in these samples. One is near the textural unconformity and is best explained by diffusive alteration during partial resorption of first stage garnet. The other occurs near the outer rim of garnet in staurolite zone samples and marks the onset of a new prograde garnet producing reaction.  相似文献   

6.
A suite of pelitic rocks around Kandra, Singhbhum District, Bihar, displays a metamorphic gradient registered by the index minerals chlorite, biotite, garnet, staurolite and sillimanite in a Barrovian sequence. Metamorphism was by and large coeval with folding movements, and correlating the internal fabric of minerals and deformational characters, a regular sequence of the index minerals is derived. It is argued that the chronological order by itself is not sufficient to prove that metamorphism was progressive in time.Among the index minerals, garnet appears to have formed by the reaction chlorite+biotitea+quartz garnet+biotiteb+H2O. For the origin of sillimanite, a new reaction, 3 staurolite+muscovite+quartz=7 sillimanite+biotite+3H2O, is suggested on the basis of significant textural features. Textural and petrological indications regarding the formation of staurolite are in discordance. Staurolite was either derived from the biotite zone phases, or should be taken to have formed, against textural evidences, from chloritoids of the garnet zone.Graphical analysis of the assemblages by Thompson's AFM projection reveals that chlorite and staurolite are excess phases owing to retrogression and incomplete reaction. Shifting of apices of triangular fields and intersection of garnet-biotite tie lines within a zone can be satisfactorily explained in terms of extra components CaO and MnO or their ratios. It is pointed out that if MgO/(MgO + FeO) between two phases show a linear relation, their tie lines will be concurrent on the AF side of the projection, the point of concurrence reflecting equilibrium and temperature of recrystallisation.  相似文献   

7.
A detailed study of retrograde alteration of a staurolite porphyroblast and its surrounding matrix of mica schist has made use of petrographic, modal, and microprobe analysis. Retrogression was to the garnet zone of metamorphism and apparently occurred largely after a temperature decline of 70–100° C. The event caused metasomatic removal of Zn but may have been isochemical relative to other analyzed elements. The best estimate of the overall reaction is: 1 staurolite+3.018 biotite+3.550 quartz+0.629 albite +0.014 anorthite+0.678 NaCl+14.004 H2O =3.274 Na-rich muscovite+3.561 chlorite +0.273 ilmenite+0.110 chloritoid+0.039 garnet +0.339 ZnCl2.Non-systematic variation in composition of analyzed minerals is revealed by statistical treatment of replicate analyses. Such variation involves monovalent and divalent cations within many minerals, but is most pronounced within retrograde muscovite. Muscovite variation involves Si and Al as well as FM and alkalis and does not follow a phengite law of charge-coupled substitution.Relative to the core of the retrograded staurolite crystal, zoning is seen in averaged muscovite compositions and in development of incompatible mineral assemblages, which include chloritoid well within retrograded staurolite but biotite within the matrix. A local gradient in the chemical potential of an Al-bearing component was likely present during retrogression.Alteration of staurolite was probably accomplished by reaction and diffusion through the medium of an intergranular fluid phase. Relative to staurolite, migration of elements involved immigration of considerable amounts of Mg, Na, K, and H and expulsion of Al, Fe, Zn, and O. It is inferred that concentration of Al within the fluid phase was considerably lower than those of monovalent and divalent cations.Preservation of considerable staurolite and evidence for a local concentration gradient of Al in the fluid phase suggest that limited amounts of H2O were available. Expulsion of Zn suggests that much water was not consumed locally but exited the terrane. An attempt at resolution of this dilemna involves fracture-channelized infiltration of H2O into the rock. A more regional petrographic study of retrogression suggests that H2O which entered the rock may have been liberated initially by prograde dehydration at a moderately greater depth of 2–3 km.Results of this study, especially the non-phengitic nature of crystal-chemical substitution within muscovite, indicate chemical reaction under conditions of disequilibrium. Apparently, extent of retrogression was controlled by availability of H2O rather than by thermochemical equilibria.  相似文献   

8.
Prograde mineral assemblages and compositions have been predicted for pelitic schist in the 10 component system Na2O–K2O–CaO–MnO–FeO–MgO–Al2O3–SiO2–CO2–H2O for three cases of prograde metamorphism and fluid-rock interaction: (1) increasing temperature (T) at constant pressure (P) and constant pore fluid volume (1%) without infiltration (no-infiltration case); (2) increasing T at constant P accompanied by sufficient fluid infiltration that fluid composition is at all times constant (large-flux case); and (3) increasing T at constantP accompanied by a timeintegrated fluid flux f 104 cm3 cm 2 (intermediate-flux case). Stable mineral assemblages and compositions were calculated by solving a system of non-linear equations that specify mass balance and chemical equilibrium between minerals and fluid. The model pelitic system includes quartz, muscovite, plagioclasc, chlorite, ankerite, siderite, biotite, garnet, staurolite, andalusite, kyanite, sillimanite, K-feldspar, and a coexisting, binary H2O–CO2 fluid. Specifically, prograde thermal metamorphism was modelled for Shaw's (1956) average low-grade pelite and for a moderate range of bulk rock compositions at P=3, 5, and 7 kb and initial fluids with Xco 2 o =0.02–0.40. The model predicts a carbonate-bearing mineral assemblage for average pelite under chlorite zone conditions composed of quartz, muscovite, albite, chlorite, ankerite, and siderite. The mineral assemblages predicted for the noinfiltration case are unlike those typically observed in regional metamorphic terranes. Simulations of metamorphism for the large-flux and intermediate-flux cases, however, reproduce the sequence of mineral assemblages observed in normal Barrovian regional metamorphic terranes. These results suggest that regional metamorphism of pelitic schists is typically associated with infiltration of significant quantities of aqueous fluid.  相似文献   

9.
《Journal of Structural Geology》2002,24(6-7):1139-1156
In metapelitic rocks of western Maine, a pluton-related M3 metamorphic gradient ranging in grade from garnet to upper sillimanite zone was superposed on a fairly uniform M2 regional metamorphic terrain characterized by the assemblage andalusite+staurolite+biotite+/−garnet. As a result, M2 assemblages re-equilibrated to the P, T, and aH2O conditions of M3, and both prograde and retrograde pseudomorphism of M2 porphyroblasts occurred. The type of pseudomorph and degree of development is directly related to the rock's position within the M3 metamorphic gradient, a function of its proximity to the Mooselookmeguntic pluton. Several ‘hinge’ zones occur in which the M3 minerals that pseudomorphed a particular M2 phase change. For example, M2 garnet was replaced by M3 chlorite or biotite, depending on its position within the M3 gradient. Similarly, in a transition zone between M3 upper staurolite and lower sillimanite zones, M2 staurolite was stable and shows M3 growth rims. Downgrade from this transition zone, staurolite was pseudomorphed by chlorite and muscovite, whereas upgrade, the pseudomorphs contain muscovite and some biotite. M3 pseudomorphs commonly retain crystal shapes of the original M2 porphyroblasts, reflecting relatively low regional deviatoric stress during and after M3. Although evidence for textural disequilibrium is common, chemical equilibrium was closely approached during M3. This study demonstrates for M3 that: (1) the pseudomorphic replacement was a constant volume process, and (2) fabrics produced by tectonic events can be erased by subsequent deformation and/or sufficiently intense subsequent recrystallization.  相似文献   

10.
Amphibolite facies mafic rocks that consist mainly of hornblende, plagioclase and quartz may also contain combinations of chlorite, garnet, epidote, and, more unusually, staurolite, kyanite, sillimanite, cordierite and orthoamphiboles. Such assemblages can provide tighter constraints on the pressure and temperature evolution of metamorphic terranes than is usually possible from metabasites. Because of the high variance of most of the assemblages, the phase relationships in amphibolites depend on rock composition, in addition to pressure, temperature and fluid composition. The mineral equilibria in the Na2O–CaO–FeO–MgO–Al2O3–SiO2–H2O (NCFMASH) model system demonstrate that aluminium content is critical in controlling the occurrence of assemblages involving hornblende with aluminous minerals such as sillimanite, kyanite, staurolite and cordierite. Except in aluminous compositions, these assemblages are restricted to higher pressures. The iron to magnesium ratio (XFe), and to a lesser extent, sodium to calcium ratio, have important roles in determining which (if any) of the aluminous minerals occur under particular pressure–temperature conditions. Where aluminous minerals occur in amphibolites, the P–T–X dependence of their phase relationships is remarkably similar to that in metapelitic rocks. The mineral assemblages of Fe‐rich amphibolites are typically dominated by garnet‐ and staurolite‐bearing assemblages, whereas their more Mg‐rich counterparts contain chlorite and cordierite. Assemblages involving staurolite–hornblende can occur over a wide range of pressures (4–10 kbar) at temperatures of 560–650 °C; however, except in the more aluminous, iron‐rich compositions, they occupy a narrow pressure–temperature window. Thus, although their occurrence in ‘typical’ amphibolites may be indicative of relatively high pressure metamorphism, in more aluminous compositions their interpretation is less straightforward.  相似文献   

11.
Interpretations based on quantitative phase diagrams in the system CaO–Na2O–K2O–TiO2–MnO–FeO–MgO–Al2O3–SiO2–H2O indicate that mineral assemblages, zonations and microstructures observed in migmatitic rocks from the Beit Bridge Complex (Messina area, Limpopo Belt) formed along a clockwise P–T path. That path displays a prograde P–T increase from 600 °C/7.0 kbar to 780 °C/9–10 kbar (pressure peak) and 820 °C/8 kbar (thermal peak), followed by a P–T decrease to 600 °C/4 kbar. The data used to construct the P–T path were derived from three samples of migmatitic gneiss from a restricted area, each of which has a distinct bulk composition: (1) a K, Al‐rich garnet–biotite–cordierite–sillimanite–K‐feldspar–plagioclase–quartz–graphite gneiss (2) a K‐poor, Al‐rich garnet–biotite–staurolite–cordierite–kyanite–sillimanite–plagioclase–quartz–rutile gneiss, and (3) a K, Al‐poor, Fe‐rich garnet–orthopyroxene–biotite–chlorite–plagioclase–quartz–rutile–ilmenite gneiss. Preservation of continuous prograde garnet growth zonation demonstrates that the pro‐ and retrograde P–T evolution of the gneisses must have been rapid, occurring during a single orogenic cycle. These petrological findings in combination with existing geochronological and structural data show that granulite facies metamorphism of the Beit Bridge metasedimentary rocks resulted from an orogenic event during the Palaeoproterozoic (c. 2.0 Ga), caused by oblique collision between the Kaapvaal and Zimbabwe Cratons. Abbreviations follow Kretz (1983 ).  相似文献   

12.
Abstract The Siluro-Devonian Waits River Formation of north-east Vermont was deformed, intruded by plutons and regionally metamorphosed during the Devonian Acadian Orogeny. Five metamorphic zones were mapped based on the mineralogy of carbonate rocks. From low to high grade, these are: (1) ankerite-albite, (2) ankerite-oligoclase, (3) biotite, (4) amphibole and (5) diopside zones. Pressure was near 4.5kbar and temperature varied from c. 450° C in the ankerite-albite zone to c. 525° C in the diopside zone. Fluid composition for all metamorphic zones was estimated from mineral equilibria. Average calculated χco2[= CO2/(CO2+ H2O)] of fluid in equilibrium with the marls increases with increasing grade from 0.05 in the ankerite-oligoclase zone, to 0.25 in the biotite zone and to 0.44 in the amphibole zone. In the diopside zone, χCO2 decreases to 0.06. Model prograde metamorphic reactions were derived from measured modes, mineral chemistry, and whole-rock chemistry. Prograde reactions involved decarbonation with an evolved volatile mixture of χCO2 > 0.50. The χCO2 of fluid in equilibrium with rocks from all zones, however, was generally <0.40. This difference attests to the infiltration of a reactive H2O-rich fluid during metamorphism. Metamorphosed carbonate rocks from the formation suggests that both heat flow and pervasive infiltration of a reactive H2O-rich fluid drove mineral reactions during metamorphism. Average time-integrated volume fluxes (cm3 fluid/cm2 rock), calculated from the standard equation for coupled fluid flow and reaction in porous media, are (1) ankerite-oligoclase zone: c. 1 × 104; (2) biotite zone: c. 3 × 104; (3) amphibole zone: c. 10 × 104; and diopside zone: c. 60 × 104. The increase in calculated flux with increasing grade is at least in part the result of internal production of volatiles from prograde reactions in pelitic schists and metacarbonate rocks within the Waits River Formation. The mapped pattern of time-integrated fluxes indicates that the Strafford-Willoughby Arch and the numerous igneous intrusions in the field area focused fluid flow during metamorphism. Many rock specimens in the diopside zone experienced extreme alkali depletion and also record low χCO2. Metamorphic fluids in equilibrium with diopside zone rocks may therefore represent a mixture of acid, H2O-rich fluids given off by the crystallizing magmas, and CO2-H2O fluids produced by devolatilization reactions in the host marls. Higher fluxes and different fluid compositions recorded near the plutons suggest that pluton-driven hydrothermal cells were local highs in the larger regional metamorphic hydrothermal system.  相似文献   

13.
Low-pressure, medium- to high-temperature (Buchan-type) regional metamorphism of pelitic rocks in the Mount Lofty Ranges, South Australia, is defined by the development of biotite, staurolite-andalusite, fibrolite, prismatic sillimanite and migmatite zones. K-feldspar makes its first appearance in the prismatic sillimanite zone and here we restrict our discussion to lower grade assemblages containing prograde muscovite, concentrating particularly on well-developed andalusitestaurolite parageneses. In general, the spatial distribution and mineral chemical variation of these assemblages accord with the predictions of petrogenetic grids and P-T and T-X Fe pseudo-sections constructed from the internally consistent data set of Holland and Powell (1990) in the system KFMASH, assuming a(H2O) 1, although analysed white mica compositions are systematically more aluminous than predicted. Importantly, the stability ranges of most critical assemblages predicted by these grids and pseudo-sections coincide closely with P-T estimates calculated using the data set of Holland and Powell (1990) from the Mount Lofty Ranges assemblages. With the exception of Mn in garnet and Zn in one staurolite-cordierite-muscovite assemblage non-KFMASH components do not significantly appear to have affected the stability ranges of the observed assemblages. An apparent local reversal in isograd zonation in which andalusite first appears down-grade of staurolite suggests a metamorphic field gradient concave towards the temperature axis and, together with evidence for essentially isobaric heating of individual rocks, is consistent with the exposures representing an oblique profile through a terrain in which heat was dissipated from intrusive bodies at discrete structural levels.Mineral abbreviations used in figures als Al2SiO5 phase - bi biotite - chl chlorite - ky kyanite - ph phengite - sill sillimanite - and andalusite - cd cordieritc - gt garnet - mu muscovite - q quartz - st staurolite  相似文献   

14.
Partial melting and retrogression related to Variscan tectonic exhumation have been recognized in the high-grade metapelites of the Tatra Mountains, Western Carpathians. Staurolite and kyanite relics document an early stage of the prograde metamorphism at c. 600 °C and 9–10 kbar. An increase in temperature to >730 °C at 11–12 kbar resulted in partial melting and incipient migmatization in the stability field of kyanite. Further heating at decreasing pressure during the earliest stage of exhumation led to the dehydration-melting of muscovite and biotite at >750–800 °C and 6–10 kbar, producing garnet-bearing granite as leucosomes in migmatite. Subsequent cooling is documented by garnet resorption by biotite and sillimanite (a reversal of the prograde biotite dehydration-melting reaction). This was followed by nearly isothermal decompression to c. 4–5 kbar producing cordierite and some melt due to biotite decomposition. Later nearly isobaric cooling led to cordierite pinitization and formation of orthoamphibole, chlorite and carbonates. Densities of primary, monophase CO2–N2 inclusions (0.69–1.06 g cm?3) from the migmatite leucosome are consistent with the near-peak and retrograde conditions. Highly varying N2 contents (5–30 mol%) are thought to result from the nitrogen uptake in retrograde K-bearing minerals, or dilution by CO2 liberated during interaction of melt-derived water with metapelite graphite. The relatively high nitrogen content, not observed until now in migmatites, could have been inherited from the high-pressure metamorphism stage. It is assumed that the water-absent composition of fluid inclusions is not representative of the bulk water content (XH2O≤0.7), which was masked by mechanical separation of the CO2- and H2O-dominated immiscible phases, and/or by post-entrapment modifications of the fluid inclusions. Decompression and the final stage of exhumation were accomplished by top-to-the-south thrusting as well as west–east (orogen-parallel) extension. They were most probably related to regional uplift and gravitational collapse of thermally weakened Variscan crust.  相似文献   

15.
During Hercynian low-pressure/high-temperature metamorphism of Palaeozoic metasediments of the southern Aspromonte (Calabria), a sequence of metamorphic zones at chlorite, biotite, garnet, staurolite–andalusite and sillimanite–muscovite grade was developed. These metasediments represent the upper part of an exposed tilted cross-section through the Hercynian continental crust. P–T information on their metamorphism supplements that already known for the granulite facies lower crust of the section and allows reconstruction of the thermal conditions in the Calabrian crust during the late Hercynian orogenic event. Three foliations formed during deformation of the metasediments. The peak metamorphic assemblages grew mainly syntectonically (S2) during regional metamorphism, but mineral growth outlasted the deformation. This is in accordance with the textural relationships found in the lower part of the same crustal section exposed in the northern Serre. Pressure conditions recorded for the base of the upper crustal metasediments are c. 2.5 kbar and estimated temperatures range from <350 °C in the chlorite zone, increasing to 500 °C in the lower garnet zone, and reaching 620 °C in the sillimanite–muscovite zone. Geothermal gradients for the peak of metamorphism indicate a much higher value for the upper crust (c. 60 °C km?1) than for the granulite facies lower crust (30–35 °C km?1). The small temperature difference between the base of the upper crust (620 °C at c. 2.5 kbar) and the top of the lower crust (690 °C at 5.5 kbar) can be explained by intrusions of granitoids into the middle crust, which, in this crustal section, took place synchronously with the regional metamorphism at c. 310– 295 Ma. It is concluded that the thermal structure of the Calabrian crust during the Hercynian orogeny – as it is reflected by peak metamorphic assemblages – was mainly controlled by advective heat input through magmatic intrusions into all levels of the crust.  相似文献   

16.
Metapelitic hornfelses in the contact aureole of the Vedrette di Ries pluton exhibit the terminal decomposition of Zn-poor Fe-staurolite in a muscovite-quartz-free domain. The reaction takes place only within coarsegrained sillimanite that has replaced andalusite porphyroblasts during prograde metamorphism. The product is a gahnite-poor hercynitic spinel, which occurs as very small grains closely associated in space with resorbed staurolite. Microstructural observations indicate that bereynite growth postdates the pseudomorphs of sillimanite after andalusite. The textural evidence for a genetic relationship between hercynite and staurolite is confirmed by the identical Fe/Mg/Zn ratios of the two minerals, which causes the collinearity of hercynite, staurolite and Al2SiO5 in FeO–MgO–ZnO–Al2O3–SiO2–H2O composition space (FMZASH), and indicates hercynite formed by the reaction: Fe-staurolite = 3.85hercynite + 5.1sillimanite + 2.55quartz + 2H2O Staurolite inclusions within andalusite did not break down to form hercynite, indicating a kinetic control, as well as little overstepping of the equilibrium conditions, of the reaction forming hercynite. Assuming overstepping did not occur, modelling of the reaction with existing thermodynamic data in the simplified FASH system suggests that the terminal breakdown of staurolite to form hercynite occurred at 2.5–3.75kbar and 585–655°C.  相似文献   

17.
Oxygen isotope analyses of quartz-Al2SiO5 pairs have been made for samples from the Mica Creek area, British Columbia. We have analysed quartz–kyanite nodules and quartz–kyanite and quartz–sillimanite in multiphase pelitic rocks from the staurolite–kyanite, kyanite, and sillimanite zones. Apparent temperatures calculated from oxygen isotopic fractionation range from 555 °C (staurolite–kyanite zone) to 695 °C (sillimanite zone). Temperatures from the quartz–kyanite nodules range from 630 to 675 °C. Some of the nodules show isotopic disequilibrium. Most of the results confirm predictions that bimineralic rocks will yield an estimate of peak metamorphic temperatures, when the less abundant mineral (an aluminium silicate) is the slower oxygen diffuser. Using cooling rates of 10–100 °C Ma?1 for the multiphase rocks, measured crystal sizes and modes, the Fast Grain Boundary diffusion model with ‘wet’ diffusion data (PH2O?1.0 kbar) yields predicted apparent temperatures which are generally lower than the measured apparent temperatures. The agreement is improved if slower diffusion coefficients are used. This suggests that f (H2O) during cooling was lower than that of the hydrothermal experiments and thus that there was little interaction with aqueous fluids of internal or external origin to modify the isotopic compositions. The measured apparent isotopic temperatures and apparent garnet–biotite Fe–Mg exchange temperatures show very poor agreement for the sillimanite zone samples, with the garnet–biotite Fe–Mg exchange temperatures generally higher than the oxygen isotope temperatures. Compared with the other calibrations that we tested the measured apparent temperatures using the Sharp calibration show the best agreeement with recently published P–T grids, although some variability in agreement is expected due to variable f (H2O) during cooling.  相似文献   

18.
ABSTRACT The high-grade rocks (metapelite, quartzite, metagabbro) of the Hisøy-Torungen area represent the south-westernmost exposures of granulites in the Proterozoic Bamble sector, south Norway. The area is isoclinally folded and a metamorphic P–T–t path through four successive stages (M1-M4) is recognized. Petrological evidence for a prograde metamorphic event (M1) is obtained from relict staurolite + chlorite + albite, staurolite + hercynite + ilmenite, cordierite + sillimanite, fine-grained felsic material + quartz and hercynite + biotite ± sillimanite within metapelitic garnet. The phase relations are consistent with a pressure of 3.6 ± 0.5 kbar and temperatures up to 750–850°C. M1 is connected to the thermal effect of the gabbroic intrusions prior to the main (M2) Sveconorwegian granulite facies metamorphism. The main M2 granulite facies mineral assemblages (quartz+ plagioclase + K-feldspar + garnet + biotite ± sillimanite) are best preserved in the several-metre-wide Al-rich metapelites, which represent conditions of 5.9–9.1 kbar and 790–884°C. These P–T conditions are consistent with a temperature increase of 80–100°C relative to the adjacent amphibolite facies terranes. No accompanying pressure variations are recorded. Up to 1-mm-wide fine-grained felsic veinlets appear in several units and represent remnants of a former melt formed by the reaction: Bt + Sil + Qtz→Grt + lq. This dehydration reaction, together with the absence of large-scale migmatites in the area, suggests a very reduced water activity in the rocks and XH2O = 0.25 in the C–O–H fluid system was calculated for a metapelitic unit. A low but variable water activity can best explain the presence or absence of fine-grained felsic material representing a former melt in the different granulitic metapelites. The strongly peraluminous composition of the felsic veinlets is due to the reaction: Grt +former melt ± Sil→Crd + Bt ± Qtz + H2O, which has given poorly crystalline cordierite aggregates intergrown with well-crystalline biotite. The cordierite- and biotite-producing reaction constrains a steep first-stage retrograde (relative to M2) uplift path. Decimetre- to metre-wide, strongly banded metapelites (quartz + plagioclase + biotite + garnet ± sillimanite) inter-layered with quartzites are retrograded to (M3) amphibolite facies assemblages. A P–T estimate of 1.7–5.6 kbar, 516–581°C is obtained from geothermobarometry based on rim-rim analyses of garnet–biotite–plagioclase–sillimanite–quartz assemblages, and can be related to the isoclinal folding of the rocks. M4 greenschist facies conditions are most extensively developed in millimetre-wide chlorite-rich, calcite-bearing veins cutting the foliation.  相似文献   

19.
The timing and thermal effects of granitoid intrusions into accreted sedimentary rocks are important for understanding the growth process of continental crust. In this study, the petrology and geochronology of pelitic gneisses in the Tseel area of the Tseel terrane, SW Mongolia, are examined to understand the relationship between igneous activity and metamorphism during crustal evolution in the Central Asian Orogenic Belt (CAOB). Four mineral zones are recognized on the basis of progressive changes in the mineral assemblages in the pelitic gneisses, namely: the garnet, staurolite, sillimanite and cordierite zones. The gneisses with high metamorphic grades (i.e. sillimanite and cordierite zones) occur in the central part of the Tseel area, where granitoids are abundant. To the north and south of these granitoids, the metamorphic grade shows a gradual decrease. The composition of garnet in the pelitic gneisses varies systematically across the mineral zones, from grossular‐rich garnet in the garnet zone to zoned garnet with grossular‐rich cores and pyrope‐rich rims in the staurolite zone, and pyrope‐rich garnet in the sillimanite and cordierite zones. Thermobarometric analyses of individual garnet crystals reveal two main stages of metamorphism: (i) a high‐P and low‐T stage (as recorded by garnet in the garnet zone and garnet cores in the staurolite zone) at 520–580 °C and 4.5–7 kbar in the kyanite stability field and (ii) a low‐P and high‐T stage (garnet rims in the staurolite zone and garnet in the sillimanite and cordierite zones) at 570–680 °C and 3.0–6.0 kbar in the sillimanite stability field. The earlier high‐P metamorphism resulted in the growth of kyanite in quartz veins within the staurolite and sillimanite zones. The U–Pb zircon ages of pelitic gneisses and granitoids reveal that (i) the protolith (igneous) age of the pelitic gneisses is c. 510 Ma; (ii) the low‐P and high‐T metamorphism occurred at 377 ± 30 Ma; and (iii) this metamorphic stage was coeval with granitoid intrusion at 385 ± 7 Ma. The age of the earlier low‐T and high‐P metamorphism is not clearly recorded in the zircon, but probably corresponds to small age peaks at 450–400 Ma. The low‐P and high‐T metamorphism continued for c. 100 Ma, which is longer than the active period of a single granitoid body. These findings indicate that an elevation of geotherm and a transition from high‐P and low‐T to low‐P and high‐T metamorphism occurred, associated with continuous emplacement of several granitoids, during the crustal evolution in the Devonian CAOB.  相似文献   

20.
Two types of biotite isograd are defined in the low-grade metamorphism of the Wazuka area, a Ryoke metamorphic terrain in the Kii Peninsula, Japan. The first, BI1, is defined by the reaction of chlorite+K-feldspar= biotite+muscovite+quartz+H2O that took place in psammitic rocks, and the second, BI2, by the continuous reaction between muscovite, chlorite, biotite and quartz in pelitic rocks. The Fe/Mg ratios of the host rocks do not significantly affect the reactions. From the paragenesis of pelitic and psammitic metamorphic rocks, the following mineral zones were established for this low-pressure regional metamorphic terrain: chlorite, transitional, chlorite-biotite, biotite, and sillimanite. The celadonite content of muscovite solid solution in pelitic rocks decreases systematically with the grade of metamorphism from 38% in the chlorite zone to 11% in the biotite zone. Low pressure does not prohibit muscovite from showing the progressive change of composition, if only rocks with appropriate paragenesis are chosen. A qualitative phase diagram of the AKF system relevant to biotite formation suggests that the higher the pressure of metamorphism, the higher the celadonite content of muscovite at BI1, which is confirmed by comparing the muscovites from the Barrovian and Ryoke metamorphism.  相似文献   

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