Experimental Study of the Melting Reaction and Genetic Mechanism of Mineral Phase Transformation in Granulite Facies Metamorphism

The high-temperature and high-pressure experiment on natural block rock indicates that dehydration-melting of hydrous biotite (Bi) and partial melting of felsic minerals in garnet-biotite-plagioclase gneiss are mainly controlled by temperature, while mineral phase transformation is not only controlled by temperature-pressure conditions but also genetically associated with hydrous mineral dehydration-melting and partial melting of felsic minerals. According to the characteristics of biotite dehydration-melting and garnet transformation reaction, three stages may be distinguished: (1) when the experimental temperature is 700℃, biotite transforms to ilmenite (Ilm) + magnetite (Mt) + H2O and garnet to magnetite (Mt); (2) when the temperature is 730-760℃, biotite is dehydrated and melted and transformed into K2O-rich melt + Ilm + Mt, and garnet, into hypersthene (Hy) + cordierite (Crd); (3) when the temperature is up to or higher than 790℃, biotite is dehydrated and melted and transformed into melt + Hy +     

Coexisting garnets and biotites from Precambrian gneisses of the south coast of Western Australia

Garnet-biotite (-cordierite) phase relations in high-grade gneisses of the south coast of Western Australia reflect at least two metamorphic episodes. Chemical uniformity of the interiors of garnet and cordierite grains suggest thorough equilibration during a major phase of metamorphism. Narrow Mg-depleted rims on garnet grain boundaries in contact with biotite or cordierite, and complementary Mg-enriched rims on contiguous cordierites are the result of subsequent retrograde re-equilibration. The absence of reaction zoning in biotites suggests more complete retrograde modification of this mineral.Comparison between granulite and amphibolite facies garnet-biotite pairs shows that Mn contents of both minerals are higher, and Ti contents of the biotites are lower, in the lower-grade rocks. These differences, although not entirely unrelated to grade, are more directly controlled by variations in host rock chemistry and modal amounts of garnet and biotite.Partitioning of Mg, Fe²⁺ and Mn between garnet and biotite is fairly uniform, with no clear differences between granulite and amphibolite facies pairs. Application of the Mg-Fe²⁺ distributions to the geothermometers devised by Perchuk, Thompson, and Goldman & Albee yields variable T estimates of 600–680°C, 580–780°C, and 475–715°C respectively, for the main metamorphism. These estimates are low compared with the T indicated for the granulite facies rocks by other evidence (i.e. > 750°C at 5 kb P_T). The Mg-Fe²⁺ distributions between contiguous garnet-biotite rims suggest that retrograde re-equilibration occurred at least 20–140°C below the T of the main metamorphism.     

Crystallization temperature of anatectic melt: An example of biotite–muscovite granite in the Rikolatvi structure,Belomorian Mobile Belt

Zircon hosted in granite, which crystallized from local pools of anatectic melt among migmatites, in the Rikolatvi structure, Belomorian Mobile Belt, contains minute inclusions of various minerals, biotite and garnet among others. The compositions of the biotite and garnet in the microinclusions differ from those of the same minerals in the granite containing the zircon. The crystallization temperature of the anatectic melt was estimated by the biotite–garnet geothermometer and the composition of the biotite and garnet inclusions at ~800°C.     

Pressure-temperature Evolution of the Metapelites in the Motuo Area,the Eastern Himalayan Syntaxis

The Motuo area is located in the east of the Eastern Himalayan Syntaxis. There outcrops a sequence of high-grade metamorphic rocks, such as metapelites. Petrology and mineralogy data suggest that these rocks have experienced three stages of metamorphism. The prograde metamorphic mineral assemblages(M1) are mineral inclusions(biotite + plagioclase + quartz ± sillimanite ± Fe-Ti oxides) preserved in garnet porphyroblasts, and the peak metamorphic assemblages(M2) are represented by garnet with the lowest XSps values and the lowest XFe# ratios and the matrix minerals(plagioclase + quartz ± Kfeldspar + biotite + muscovite + kyanite ± sillimanite), whereas the retrograde assemblages(M3) are composed of biotite + plagioclase + quartz symplectites rimming the garnet porphyroblasts. Thermobarometric computation shows that the metamorphic conditions are 562–714°C at 7.3–7.4 kbar for the M1 stage, 661–800°C at 9.4–11.6 kbar for the M2 stage, and 579–713°C at 5.5–6.6 kbar for the M3 stage. These rocks are deciphered to have undergone metamorphism characterized by clockwise P-T paths involving nearly isothermal decompression(ITD) segments, which is inferred to be related to the collision of the India and Eurasia plates.     

Separate or shared metamorphic histories of eclogites and surrounding rocks? An example from the Bohemian Massif

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.     

Magmatic garnet in the Triassic (215 Ma) Dehnow pluton of NE Iran and its petrogenetic significance

The Triassic Dehnow pluton of NE Iran is a garnet-bearing I-type calc-alkaline metaluminous diorite-tonalite-granodiorite intrusion. The parental magma formed as the result of partial melting of intermediate to felsic rocks in the lower crust. Petrological and geochemical evidence, which indicates a magmatic origin for the garnet, includes: large size (~10–20 mm) of crystals, absence of reaction rims, a distinct composition from garnet in adjacent metapelitic rocks, and similarity in the composition of mineral inclusions (biotite, hornblende) in the garnet and in the matrix. Absence of garnet-bearing enclaves in the pluton and lack of sillimanite (fibrolite) and cordierite inclusions in magmatic garnet suggests that the garnet was not produced by assimilation of meta-sedimentary country rocks. Also, the δ¹⁸O values of garnet in the pluton (8.3–8.7‰) are significantly lower than δ¹⁸O values of garnet in the metapelitic rocks (12.5–13.1‰). Amphibole-plagioclase and garnet-biotite thermometers indicate crystallization temperatures of 708°C and 790°C, respectively. A temperature of 692°C obtained by quartz-garnet oxygen isotope thermometry points to a closure temperature for oxygen diffusion in garnet. The composition of epidote (X_ep) and garnet (X_adr) indicates ~800°C for the crystallization temperature of these minerals. Elevated andradite content in the rims of garnet suggests that oxygen fugacity increased during crystallization.     

Contact metamorphic P–T–t paths from Sm–Nd garnet ages, phase equilibria modelling and thermobarometry: Garnet Ledge, south-eastern Alaska, USA

Sm–Nd garnet‐whole rock geochronology, phase equilibria, and thermobarometry results from Garnet Ledge, south‐eastern Alaska, provide the first precisely constrained P–T–t path for garnet zone contact metamorphism. Garnet cores from two crystals and associated whole rocks yield a four point isochron age for initial garnet growth of 89.9 ± 3.6 Ma. Garnet rims and matrix minerals from the same samples yield a five point isochron age for final garnet growth of 89 ± 1 Ma. Six size fractions of zircon from the adjacent pluton yield a concordant U–Pb age of 91.6 ± 0.5 Ma. The garnet core and rim, and zircon ages are compatible with single‐stage garnet growth during and/or after pluton emplacement. All garnet core–whole rock and garnet rim‐matrix data from the two samples constrain garnet growth duration to ≤5.5 my. A garnet mid‐point and the associated matrix from one of the two garnet crystals yield an age of 90.0 ± 1.0 Ma. This mid‐point result is logically younger than the 90.7 ± 5.6 Ma core–whole rock age and older than the 88.4 ± 2.5 Ma rim‐matrix age for this sample. A MnNaCaKFMASH phase diagram (P–T pseudosection) and the garnet core composition are used to predict that cores of garnet crystals grew at 610 ± 20 °C and 5 ± 1 kbar. This exceeds the temperature of the garnet‐in reaction by c. 50 °C and is compatible with overstepping of the garnet growth reaction during contact metamorphism. Intersection of three reactions involving garnet‐biotite‐sillimanite‐plagioclase‐quartz calculated by THERMOCALC in average P–T mode, and exchange thermobarometry were used to estimate peak metamorphic conditions of 678 ± 58 °C at 6.1 ± 0.9 kbar and 685 ± 50 °C at 6.3 ± 1 kbar, respectively. Integration of pressure, temperature, and age estimates yields a pressure‐temperature‐time path compatible with near isobaric garnet growth over an interval of c. 70 °C and c. 2.3 my.     

On the interpretation of peak metamorphic temperatures in light of garnet diffusion during cooling

Abstract Finite difference models of Fe-Mg diffusion in garnet undergoing cooling from metamorphic peak conditions are used to infer the significance of temperatures calculated using garnet-biotite Fe-Mg exchange thermometry. For rocks cooled from high grades where the garnet was initially homogeneous, the calculated temperature (T_calc) using garnet core and matrix biotite depends on the size of the garnet, the ratio of garnet to biotite in the rock (V_garnet/V_biotite) and the cooling rate. For garnets with radii of 1 mm and V_garnet/V_biotite<1, T_calc is 633, 700 and 777°C for cooling rates of 1, 10 and 100°C/Ma. For V_garnet/V_biotite= 1 and 4 and a cooling rate of 10° C/Ma, T_calc is approximately 660 and 610° C, respectively. Smaller and larger garnets have lower and higher T_calc, respectively. These results suggest that peak metamorphic temperatures may be reliably attained from rocks crystallized at conditions below T_calc of the garnet core, provided that V_garnet/V_biotite is sufficiently small (<0.1) and that the composition of the biotite at the metamorphic peak has not been altered during cooling. Numerical experiments on amphibolite facies garnets with nominal peak temperatures of 550–600° C generate a ‘well’in Fe/(Fe + Mg) near the rim during cooling. Maximum calculated temperatures for the assemblage garnet + chlorite + biotite + muscovite + plagioclase + quartz using the Fe/(Fe + Mg) at the bottom of the ‘well’with matrix biotite range from 23–43° C to 5–12° C below the peak metamorphic temperature for cooling rates of 1 and 100° C/Ma, respectively. Maximum calculated temperatures for the assemblage garnet + staurolite + biotite + muscovite + plagioclase + quartz are approximately 70° C below the peak metamorphic temperature and are not strongly dependent on cooling rate. The results of this study indicate that it may be very difficult to calculate peak metamorphic temperatures using garnet-biotite Fe-Mg exchange thermometry on amphibolite facies rocks (T_max > 550° C) because the rim composition of the garnet, which is required to calculate the peak temperature, is that most easily destroyed by diffusion.     

Staurolite porphyroblast controls on local bulk compositional and microstructural changes during decompression of a St–Bt–Grt–Crd–And schist (Ancasti metamorphic complex,Sierras Pampeanas,W Argentina)

The staurolite–biotite–garnet–cordierite–andalusite–plagioclase–muscovite–quartz metapelitic mineral assemblage has been frequently interpreted in the literature as a result of superimposition of various metamorphic events, for example, in polymetamorphic sequences. The assemblage was identified in schists from the Ancasti metamorphic complex (Sierras Pampeanas of Argentina) where previous authors have favoured the polymetamorphic genetic interpretation. A pseudosection in the MnNCKFMASH system for the analysed XRF bulk composition predicts the stability of the sub‐assemblage staurolite–biotite–garnet–plagioclase–muscovite–quartz, and the compositional isopleths also agree with measured mineral compositions. Nevertheless, the XRF pseudosection does not predict any field with staurolite, andalusite and cordierite being stable together. As a result of more detailed modelling making use of the effective bulk composition concept, our interpretation is that the staurolite–biotite–garnet–plagioclase–muscovite–quartz sub‐assemblage was present at peak metamorphic conditions, 590 °C and 5.2 kbar, but that andalusite and cordierite grew later along a continuous P–T path. These minerals are not in mutual contact and are observed in separate microstructural domains with different proportions of staurolite. These domains are explained as a result of local reaction equilibrium subsystems developed during decompression and influenced by the previous peak crystal size and local modal distribution of staurolite porphyroblasts that have remained metastable. Thus, andalusite and cordierite grew synchronously, although in separate microdomains, and represent the decompression stage at 565 °C and 3.5 kbar.     

Contrasting behaviour of rare earth and major elements during partial melting in granulite facies migmatites, Wuluma Hills, Arunta Block, central Australia

Low‐P granulite facies metapelitic migmatites in the Wuluma Hills, Strangways Metamorphic Complex, Arunta Block, preserve evidence of polyphase deformation and migmatite formation which is of the same age of the c. 1730 Ma Wuluma granite. Mineral equilibria modelling of garnet‐orthoproxene‐cordierite‐bearing assemblages using thermocalc is consistent with peak S3 conditions of 6.0–6.5 kbar and 850–900 °C. The growth of orthopyroxene and garnet was primarily controlled by biotite breakdown during partial melting reactions. Whereas orthopyroxene in the cordierite‐biotite mesosome shows enrichment of heavy‐REE (HREE) relative to medium‐REE (MREE), orthopyroxene in adjacent garnet‐bearing leucosome shows depletion of HREE relative to MREE. There is no appreciable difference in major element contents of minerals common to both the mesosome and leucosome. The REE variations can be satisfactorily explained by decoupling of major element and REE partitioning, in the context of appropriate phase‐equilibria modelling of a prograde path at ～6 kbar. Sparse garnet nucleii formed at ～760 °C, along with concentrated leucosome development and preferentially partitioned HREE. Further heating to ～800 °C at constant or subtly increasing pressure conditions additionally stabilized orthopyroxene and decreased the garnet mode. Orthopyroxene in the leucosome inherited an REE pattern consequent to the partial consumption of garnet, it being distinct from the REE pattern in mesosome orthoproxene that was mostly controlled by biotite breakdown. Such within‐sample variability in the enrichment of heavy REE indicates that caution needs to be exercised in the application of common elemental partitioning coefficients in spatially complex metamorphic rocks.     

Prograde pressure–temperature paths in the pelitic schists of the Sambagawa metamorphic belt, SW Japan

Prograde P–T paths recorded by the chemistry of minerals of subduction‐related metamorphic rocks allow inference of tectonic processes at convergent margins. This paper elucidates the changing P–T conditions during garnet growth in pelitic schists of the Sambagawa metamorphic belt, which is a subduction related metamorphic belt in the south‐western part of Japan. Three types of chemical zoning patterns were observed in garnet: Ca‐rich normal zoning, Ca‐poor normal zoning and intrasectoral zoning. Petrological studies indicate that normally‐zoned garnet grains grew keeping surface chemical equilibrium with the matrix, in the stable mineral assemblage of garnet + muscovite + chlorite + plagioclase + paragonite + epidote + quartz ± biotite. Pressure and temperature histories were inversely calculated from the normally‐zoned garnet in this assemblage, applying the differential thermodynamic method (Gibbs' method) with the latest available thermodynamic data set for minerals. The deduced P–T paths indicate slight increase of temperature with increasing pressure throughout garnet growth, having an average dP/dT of 0.4–0.5 GPa/100 °C. Garnet started growing at around 470 °C and 0.6 GPa to achieve the thermal and baric peak condition near the rim (520 °C, 0.9 GPa). The high‐temperature condition at relatively low pressure (for subduction related metamorphism) suggests that heating occurred before or simultaneously with subduction.     

Paleoproterozoic migmatitic gneisses from the Tandilia belt (Argentina), Río de la Plata craton,record cooling at deep crustal levels

We studied high-grade metamorphic rocks of the El Cristo hill area of the Tandilia belt. Mineral analyses and thermodynamic calculations were carried out for two adjacent rock samples: an amphibole–biotite gneiss and a garnet–biotite-bearing migmatite. Peritectic garnets in the migmatite show core compositions of pyr_4.5(gro + andr)₁₀spes₆alm_79.5 changing to pyr_3.5(gro + andr)₁₇spes₆alm_73.5 at their thin rims. Garnet compositions in the gneiss are pyr_6.5(gro + andr)₂₆spes₁₂alm_55.5 and pyr_4.5(gro + andr)₃₄spes₁₂alm_49.5 for core and rim, respectively. A P–T path was constructed by calculating pseudosections in the 11-component system Si–Ti–Al–Fe–Mn–Mg–Ca–Na–K–O–H and contouring them by isopleths for garnet components using the PERPLE_X software package. Supra-solidus crystallization of garnet cores in the migmatite began at 5.8 kbar and 660 °C. Garnet rims equilibrated at 7.0 kbar and 640 °C compatible with garnet cores in the amphibole–biotite gneiss (7.6 kbar and 660 °C). The further chemical development of garnet in this rock points to P–T conditions of 11.6 kbar and 620 °C and 12.2 kbar and 595 °C (outermost garnet rim). At this high-pressure stage Ca-amphibole was not stable. Most biotite formed during exhumation whereas the high-pressure accessory minerals, titanite and epidote, persisted. According to the obtained anti-clockwise P–T path the originally partly melted material was tectonically transported from ∼22 km (middle crust) to ∼40 km (lower crust) depths reaching a geothermal gradient as low as 15 °C km⁻¹. This transport probably occurred along a major suture zone, which was active during the Paleoproterozoic (2.25–2.10 Ga), before a terminating collision of terranes near the SW boundary of the Rio de la Plata craton.     

Prograde and retrograde history of eclogites from the Eastern Blue Ridge, North Carolina, USA

Abstract The prograde metamorphism of eclogites is typically obscured by chemical equilibration at peak conditions and by partial requilibration during retrograde metamorphism. Eclogites from the Eastern Blue Ridge of North Carolina retain evidence of their prograde path in the form of inclusions preserved in garnet. These eclogites, from the vicinity of Bakersville, North Carolina, USA are primarily comprised of garnet–clinopyroxene–rutile–hornblende–plagioclase–quartz. Quartz, clinopyroxene, hornblende, rutile, epidote, titanite and biotite are found as inclusions in garnet cores. Included hornblende and clinopyroxene are chemically distinct from their matrix counterparts. Thermobarometry of inclusion sets from different garnets record different conditions. Inclusions of clinozoisite, titanite, rutile and quartz (clinozoisite + titanite = grossular + rutile + quartz + H₂O) yield pressures (6–10 kbar, 400–600 °C and 8–12 kbar 450–680 °C) at or below the minimum peak conditions from matrix phases (10–13 kbar at 600–800 °C). Inclusions of hornblende, biotite and quartz give higher pressures (13–16 kbar and 630–660 °C). Early matrix pyroxene is partially or fully broken down to a diopside–plagioclase symplectite, and both garnet and pyroxene are rimmed with plagioclase and hornblende. Hypersthene is found as a minor phase in some diopside + plagioclase symplectites, which suggests retrogression through the granulite facies. Two‐pyroxene thermometry of this assemblage gives a temperature of c. 750 °C. Pairing the most Mg‐rich garnet composition with the assemblage plagioclase–diopside–hypersthene–quartz gives pressures of 14–16 kbar at this temperature. The hornblende–plagioclase–garnet rim–quartz assemblage yields 9–12 kbar and 500–550 °C. The combined P–T data show a clockwise loop from the amphibolite to eclogite to granulite facies, all of which are overprinted by a texturally late amphibolite facies assemblage. This loop provides an unusually complete P–T history of an eclogite, recording events during and following subduction and continental collision in the early Palaeozoic.     

Coexisting chloritoid-staurolite from the Sillimanite (fibrolite) zone,Sini, district Singhbhum,India

Microprobe analyses of the minerals from an unusual chloritoid-staurolite-garnet (+ muscovite + quartz + ilmenite) assemblage from the sillimanite (fibrolite) zone of Sini, India are presented and the petrological significance of the paragenesis is discussed. The X Mg in the different minerals from the chloritoid-staurolite-bearing rock varies in the order, muscovite > chlorite > chloritoid > staurolite > garnet > ilmenite, and from the associated sillimanite-bearing schists: muscovite > biotite > staurolite > garnet rim > garnet core > ilmenite. A graphical representation of the mineral compositions in an AFM projection displays a consistent topology if the effects of non-AFM components such as Zn in the staurolite and Mn in the garnet are taken into account. Petrographic and mineralogical data are consistent with a prograde formation of the chloritoid-staurolite-garnet assemblage. It is suggested that the paragenesis has been formed at similar PT conditions to the associated sillimanite (fibrolite)-staurolite-garnet-mica schists. These conditions are estimated to be 600–625°C/6±0.5 Kb.     

The ultra‐high pressure coronitic and pseudomorphous reactions in a metagranodiorite from the Brossasco‐Isasca Unit,Dora‐Maira Massif,western Italian Alps: a petrographic study and equilibrium thermodynamic modelling

Metagranodiorite samples from the Brossasco‐Isasca Unit, Dora‐Maira Massif, western Alps, show pseudomorphous and coronitic textures where igneous minerals were partially replaced by ultra‐high pressure (UHP) metamorphic assemblages. The original magmatic paragenesis consisted of quartz, plagioclase, K‐feldspar, biotite and minor phases. During UHP metamorphism, the plagioclase (site P) was replaced by zoisite, jadeite, quartz, K‐feldspar and kyanite, and coronitic reactions developed between biotite and adjacent minerals. At the original igneous biotite–quartz contact (site A), a single corona of poorly zoned garnet is developed, whereas at the biotite–K‐feldspar (site B) and biotite–plagioclase (site C) contacts, composite coronas are formed. Integration of results from petrographic observations, calculations of mineral stoichiometry and thermodynamic calculations of mineral stability has allowed the determination of the metamorphic reactions involved and the estimation of the metamorphic conditions, which reached as high as 24 kbar and 650 °C. Accurate microanalysis by energy‐dispersive spectroscopy (EDS) and statistical analysis of the data allowed us to identify, for the first time in a natural Na‐pyroxene of metagranitoid rocks, the end‐member Ca‐Eskola.     

Prograde metamorphic sequence of REE minerals in pelitic rocks of the Central Alps: implications for allanite–monazite–xenotime phase relations from 250 to 610 °C

The distribution of REE minerals in metasedimentary rocks was investigated to gain insight into the stability of allanite, monazite and xenotime in metapelites. Samples were collected in the central Swiss Alps, along a well‐established metamorphic field gradient that record conditions from very low grade metamorphism (250 °C) to the lower amphibolite facies (～600 °C). In the Alpine metapelites investigated, mass balance calculations show that LREE are mainly transferred between monazite and allanite during the course of prograde metamorphism. At very low grade metamorphism, detrital monazite grains (mostly Variscan in age) have two distinct populations in terms of LREE and MREE compositions. Newly formed monazite crystallized during low‐grade metamorphism (<440 °C); these are enriched in La, but depleted in Th and Y, compared with inherited grains. Upon the appearance of chloritoid (～440–450 °C, thermometry based on chlorite–choritoid and carbonaceous material), monazite is consumed, and MREE and LREE are taken up preferentially in two distinct zones of allanite distinguishable by EMPA and X‐ray mapping. Prior to garnet growth, allanite acquires two growth zones of clinozoisite: a first one rich in HREE + Y and a second one containing low REE contents. Following garnet growth, close to the chloritoid–out zone boundary (～556–580 °C, based on phase equilibrium calculations), allanite and its rims are partially to totally replaced by monazite and xenotime, both associated with plagioclase (± biotite ± staurolite ± kyanite ± quartz). In these samples, epidote relics are located in the matrix or as inclusions in garnet, and these preserve their characteristic chemical and textural growth zoning, indicating that they did not experience re‐equilibration following their prograde formation. Hence, the partial breakdown of allanite to monazite offers the attractive possibility to obtain in situ ages, representing two distinct crystallization stages. In addition, the complex REE + Y and Th zoning pattern of allanite and monazite are essential monitors of crystallization conditions at relatively low metamorphic grade.     

Mineral evolution of a garnet-pyroxenite nodule within eclogite, eastern Sulu ultrahigh-pressure metamorphic terrane, East China

Detailed microtextural observations and bulk chemical analysis were undertaken on a garnet‐pyroxenite nodule within retrograde eclogites from the NE Sulu ultrahigh‐pressure metamorphic (UHPM) terrane. The results suggest that the protolith was a cumulate from a gabbroic body. The nodule consists primarily of coarse clinopyroxene grains with a very high content of the Ca‐Tschermakite molecule. Microscopic observations and back‐scattered electron images (BSE) demonstrate a complicated intergrowth of clinopyroxene, garnet and ilmenite, which represents the peak metamorphic assemblage. The primary clinopyroxene grains are armoured with a thin garnet corona up to 0.5 mm wide that forms an interconnected network. Within the clinopyroxene grains, four sets of garnet lamellae are distributed along crystallographic planes; locally, a vermicular intergrowth of garnet and diopside is developed. Besides the garnet, parallel arrays of ilmenite blebs are common within the clinopyroxene. Hydrous minerals such as amphibole, zoisite and titanite formed at later stages, and replaced diopside, garnet and ilmenite respectively. The P–T conditions determined for the formation of the garnet lamellae indicate that the garnet pyroxenite experienced UHP metamorphism at the same peak P–T condition as its host eclogite. The very high Ca‐Tschermakite content (31–34 mol.%) of the primary clinopyroxene indicates crystallization at about 9–17 kbar and 1250–1450 °C, and together with the microtextural observations, suggests that the protolith of the garnet pyroxenite was a cumulate from a former gabbroic body, in which case, the host eclogite might represent the gabbroic body.     

Formation of elliptical garnet in a metapelitic enclave by melt-assisted dissolution and reprecipitation

Metapelitic residual enclaves in the Neogene Volcanic Province of SE Spain are residues left after melt extraction. Glass (quenched melt) of granitic composition occurs as inclusions in most minerals and as intergranular pockets. The most common enclave types show one stage of garnet growth that is interpreted to have occurred at the same time as glass production. Some of these show a well‐developed foliation outlined by fibrolite, biotite, graphite and glass, which wraps around elongate garnet crystals that have aspect ratios up to 10:1. Based on microstructures and chemistry, the garnet within these rocks shows clear core and mantle structure. The core has an average composition of Alm₇₆–Prp₀₈–Sps₁₄–Grs₀₃ and contains primary inclusions of biotite and melt, trapped during garnet growth. A thin (c. 100 μm), irregular mantle overgrows the garnet core, enclosing oriented fibrolite inclusions in strain caps, and biotite in strain shadows. In places, the overgrowths form skeletal elongated arms, which extend parallel to the foliation. The garnet mantle contains less Mn and higher X_Mg, but both core and mantle display flat Mn profiles, the contact being a sharp break. Ternary feldspar and Grt–Bt thermometry yield temperatures in the range 800–900 °C, with no systematic differences among the different microstructural domains of elliptical garnet. Based on the observed intracrystalline microstructures, the high amount of melt extraction in the rock by flattening component strain and the chemical zoning of garnet, the formation of elliptical garnet is modelled by a multistage sequence. This involves pressure solution and reprecipitation of the core, followed by post‐kinematic, partly mimetic growth of the garnet mantle.     

Metamorphic history of eclogites and country rock gneisses in the Aktyuz area,Northern Tien‐Shan,Kyrgyzstan: a record from initiation of subduction through to oceanic closure by continent–continent collision

Eclogites and related high‐P metamorphic rocks occur in the Zaili Range of the Northern Kyrgyz Tien‐Shan (Tianshan) Mountains, which are located in the south‐western segment of the Central Asian Orogenic Belt. Eclogites are preserved in the cores of garnet amphibolites and amphibolites that occur in the Aktyuz area as boudins and layers (up to 2000 m in length) within country rock gneisses. The textures and mineral chemistry of the Aktyuz eclogites, garnet amphibolites and country rock gneisses record three distinct metamorphic events (M1–M3). In the eclogites, the first MP–HT metamorphic event (M1) of amphibolite/epidote‐amphibolite facies conditions (560–650 °C, 4–10 kbar) is established from relict mineral assemblages of polyphase inclusions in the cores and mantles of garnet, i.e. Mg‐taramite + Fe‐staurolite + paragonite ± oligoclase (An_<16) ± hematite. The eclogites also record the second HP‐LT metamorphism (M2) with a prograde stage passing through epidote‐blueschist facies conditions (330–570 °C, 8–16 kbar) to peak metamorphism in the eclogite facies (550–660 °C, 21–23 kbar) and subsequent retrograde metamorphism to epidote‐amphibolite facies conditions (545–565 °C and 10–11 kbar) that defines a clockwise P–T path. thermocalc (average P–T mode) calculations and other geothermobarometers have been applied for the estimation of P–T conditions. M3 is inferred from the garnet amphibolites and country rock gneisses. Garnet amphibolites that underwent this pervasive HP–HT metamorphism after the eclogite facies equilibrium have a peak metamorphic assemblage of garnet and pargasite. The prograde and peak metamorphic conditions of the garnet amphibolites are estimated to be 600–640 °C; 11–12 kbar and 675–735 °C and 14–15 kbar, respectively. Inclusion phases in porphyroblastic plagioclase in the country rock gneisses suggest a prograde stage of the epidote‐amphibolite facies (477 °C and 10 kbar). The peak mineral assemblage of the country rock gneisses of garnet, plagioclase (An_11–16), phengite, biotite, quartz and rutile indicate 635–745 °C and 13–15 kbar. The P–T conditions estimated for the prograde, peak and retrograde stages in garnet amphibolite and country rock are similar, implying that the third metamorphic event in the garnet amphibolites was correlated with the metamorphism in the country rock gneisses. The eclogites also show evidence of the third metamorphic event with development of the prograde mineral assemblage pargasite, oligoclase and biotite after the retrograde epidote‐amphibolite facies metamorphism. The three metamorphic events occurred in distinct tectonic settings: (i) metamorphism along the hot hangingwall at the inception of subduction, (ii) subsequent subduction zone metamorphism of the oceanic plate and exhumation, and (iii) continent–continent collision and exhumation of the entire metamorphic sequences. These tectonic processes document the initial stage of closure of a palaeo‐ocean subduction to its completion by continent–continent collision.     

Apparent oxygen isotope equilibrium during progressive foliation development and porphyroblast growth in metapelites: implications for stable isotope and conventional thermometry

The assumption of oxygen isotope and major element equilibrium during prograde metamorphism was tested using staurolite‐grade pelitic schists that have undergone sequential porphyroblast growth and multiple episodes of recrystallization of matrix minerals and foliation development. Textural relationships are used to infer a metamorphic history that involves garnet growth followed by staurolite growth, with each porphyroblast growth event followed by at least one period of recrystallization of matrix minerals. Conventional geothermobarometry using Qtz–Grt–Pl–Ms–Bt ± St equilibria yields peak P–T conditions of c. 625 °C at 9–11 kbar, consistent with KMnFMASH petrogenetic grid predictions for stability of the assemblage Grt + St + Bt. Qtz–Grt oxygen isotope fractionations yield apparent temperatures of c. 590 °C and Qtz–St fractionations yield an apparent temperature of c. 595 °C. Diffusional modelling indicates that quartz isotopic compositions were reset by c. 30 °C via retrograde isotopic diffusional exchange with micas. The isotopic temperatures appear to be in excellent agreement with one another, and suggest oxygen isotope equilibrium was attained between garnet and staurolite at c. 625 °C. However, the agreement of Qtz–Grt and Qtz–Str isotopic temperatures is not consistent with petrographic observations (garnet grew before staurolite) and petrogenetic grid constraints that predict that garnet grows over a temperature interval of c. 525–550 °C. Given that: (i) oxygen diffusion rates in staurolite and garnet are slow enough to render an individual porphyroblast effectively closed to exchange after it forms; and (ii) matrix minerals are able to exchange isotopes via recrystallization during each period of deformation; garnet and staurolite could not have simultaneously achieved oxygen isotope equilibrium with each other or with minerals in the recrystallized matrix. Thus, the Qtz–Grt fractionations, which yield apparent temperatures that are in apparent agreement with peak metamorphic temperature and apparent temperatures for Qtz–St fractionations, cannot be fractionations resulting from equilibrium isotopic exchange. Instead, they are apparent fractionations between porphyroblasts formed at different temperature and times in the prograde P–T–D path, and quartz that recrystallized and exchanged with micas and plagioclase during several phases of deformation.