Phase equilibria constraints on melting of stromatic migmatites from Ronda (S. Spain): insights on the formation of peritectic garnet

Stromatic metatexites occurring structurally below the contact with the Ronda peridotite (Ojén nappe, Betic Cordillera, S Spain) are characterized by the mineral assemblage Qtz+Pl+Kfs+Bt+Sil+Grt+Ap+Gr+Ilm. Garnet occurs in low modal amount (2–5 vol.%). Very rare muscovite is present as armoured inclusions, indicating prograde exhaustion. Microstructural evidence of melting in the migmatites includes pseudomorphs after melt films and nanogranite and glassy inclusions hosted in garnet cores. The latter microstructure demonstrates that garnet crystallized in the presence of melt. Re‐melted nanogranites and preserved glassy inclusions show leucogranitic compositions. Phase equilibria modelling of the stromatic migmatite in the MnO–Na₂O–CaO–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂–O₂–C (MnNCaKFMASHOC) system with graphite‐saturated fluid shows P–T conditions of equilibration of 4.5–5 kbar, 660–700 °C. These results are consistent with the complete experimental re‐melting of nanogranites at 700 °C and indicate that nanogranites represent the anatectic melt generated immediately after entering supersolidus conditions. The P–T estimate for garnet and melt development does not, however, overlap with the low‐temperature tip of the pure melt field in the phase diagram calculated for the composition of preserved glassy inclusions in garnet in the Na₂O–CaO–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O (NCKFMASH) system. A comparison of measured melt compositions formed immediately beyond the solidus with results of phase equilibria modelling points to the systematic underestimation of FeO, MgO and CaO in the calculated melt. These discrepancies are present also when calculated melts are compared with low‐T natural and experimental melts from the literature. Under such conditions, the available melt model does not perform well. Given the presence of melt inclusions in garnet cores and the P–T estimates for their formation, we argue that small amounts (<5 vol.%) of peritectic garnet may grow at low temperatures (≤700 °C), as a result of continuous melting reactions consuming biotite.     

Regional-scale Grenvillian-age UHT metamorphism in the Mollendo–Camana block (basement of the Peruvian Andes)

The Mollendo–Camana Block (MCB) is a 50 × 150 km Precambrian inlier of the Andean belt that outcrops along the Pacific coast of southern Peru. It consists of stromatic migmatites of Paleoproterozoic heritage intensely metamorphosed during the Grenville event (c. 1 Ga; U‐Pb and U‐Th‐Pb ages on zircon and monazite). In the migmatites, aluminous mesosomes (FMAS) and quartzofeldspathic leucosomes (KFMASH), contain various amounts of K‐feldspar (Kfs), orthopyroxene (X_Mg Opx = 0.86), plagioclase (Pl), sillimanite (Sil; exceptionally kyanite, Ky) ilmenite (Ilm), magnetite (Mag), quartz (Qtz), and minor amounts of garnet (X_Mg Grt = 0.60), sapphirine (X_Mg Spr = 0.87), cordierite (X_Mg Crd = 0.92) and biotite (X_Mg Bt = 0.83). The ubiquitous peak mineral assemblage is Opx‐Sil‐Kfs‐Qtz‐(± Grt) in most of the MCB, which, together with the high Al content of orthopyroxene (10% Al₂O₃) and the local coexistence of sapphirine‐quartz, attest to regional UHT metamorphism (> 900 °C) at pressures in excess of 1.0 GPa. Fluid‐absent melting of biotite is responsible for the massive production of orthopyroxene that proceeded until exhaustion of biotite (and most of the garnet) in the southern part of the MCB (Mollendo‐Cocachacra areas). In this area, a first stage of decompression from 1.1–1.2 to 0.8–0.9 GPa at temperatures in excess of 950 °C, is marked by the breakdown of Sil‐Opx to Spr‐Opx‐Crd assemblages according to several bivariant FMAS reactions. High‐T decompression is also shown by Mg‐rich garnet being replaced by Crd‐Spr‐ and Crd‐Opx‐bearing symplectites, and reacting with quartz to produce low‐Al‐Opx‐Sil symplectites in quartz‐rich migmatites. Neither osumilite nor spinel‐quartz assemblages being formed, isobaric cooling at about 0.9 GPa probably followed the initial decompression and proceeded with massive precipitation of melts towards the (Os) invariant point, as demonstrated by Bt‐Qtz‐(± pl) symplectites in quartz‐rich migmatites (melt + Opx + Sil = Bt + Grt + Kfs + Qtz). Finally, Opx rims around secondary biotite attest to late fluid‐absent melting, compatible with a second stage of decompression below 900 °C. The two stages of decompression are interpreted as due to rapid tectonic denudation whereas the regional extent of UHT metamorphism in the area, probably results from large‐scale penetration of hot asthenospheric mantle at the base of an over‐thickened crust.     

Low‐P and high‐T metamorphism of basalts: Insights from the Sudbury impact melt sheet aureole and thermodynamic modelling

Low‐pressure and high‐temperature (LP–HT) metamorphism of basaltic rocks, which occurs globally and throughout geological time, is rarely constrained by forward phase equilibrium modelling, yet such calculations provide valuable supplementary thermometric information and constraints on anatexis that are not possible to obtain from conventional thermometry. Metabasalts along the southern margin of the Sudbury Igneous Complex (SIC) record evidence of high‐grade contact metamorphism involving partial melting and melt segregation. Peak metamorphic temperatures reached at least ~925°C at ~1–3 kbar near the SIC contact. Preservation of the peak mineral assemblage indicates that most of the generated melt escaped from these rocks leaving a residuum characterized by a plagioclase–orthopyroxene–clinopyroxene–ilmenite‐magnetite±melt assemblage. Peak temperatures reached ~875°C up to 500 m from the SIC lower contact, which marks the transition to metabasalts that only experienced incipient partial melting without melt loss. Metabasalts ~500 to 750 m from the SIC contact are characterized by a similar two‐pyroxene mineral assemblage, but typically contain abundant hornblende that overgrew clino‐ and orthopyroxene along an isobaric cooling path. Metabasalts ~750 to 1,000 m from the SIC contact are characterized by a hornblende–plagioclase–quartz–ilmenite assemblage indicating temperatures up to ~680°C. Mass balance and phase equilibria calculations indicate that anatexis resulted in 10–20% melt generation in the inner ~500 m of the aureole, with even higher degrees of melting towards the contact. Comparison of multiple models, experiments, and natural samples indicates that modelling in the Na₂O–CaO–FeO–MgO–Al₂O₃–SiO₂–H₂O–TiO₂–O₂ (NCFMASHTO) system results in the most reliable predictions for the temperature of the solidus. Incorporation of K₂O in the most recent amphibole solution model now successfully predicts dehydration melting by the coexistence of high‐Ca amphibole and silicate melt at relatively low pressures (~1.5 kbar). However, inclusion of K₂O as a system component results in prediction of the solidus at too low a temperature. Although there are discrepancies between modelling predictions and experimental results, this study demonstrates that the pseudosection approach to mafic rocks is an invaluable tool to constrain metamorphic processes at LP–HT conditions.     

Fluid‐fluxed melting and melt loss in a syntectonic contact metamorphic aureole from the Variscan eastern Pyrenees

Open‐system behaviour through fluid influx and melt loss can produce a variety of migmatite morphologies and mineral assemblages from the same protolith composition. This is shown by different types of granulite facies migmatite from the contact aureole of the Ceret gabbro–diorite stock in the Roc de Frausa Massif (eastern Pyrenees). Patch, stromatic and schollen migmatites are identified in the inner contact aureole, whereas schollen migmatites and residual melanosomes are found as xenoliths inside the gabbro–diorite. Patch and schollen migmatites record D1 and D2 structures in folded melanosome and mostly preserve the high‐T D2 in granular or weakly foliated leucosome. Stromatic migmatites and residual melanosomes only preserve D2. The assemblage quartz–garnet–biotite–sillimanite–cordierite±K‐feldspar–plagioclase is present in patch and schollen migmatites, whereas stromatic migmatites and residual melanosomes contain a sub‐assemblage with no sillimanite and/or K‐feldspar. A decrease in X _Fe (molar Fe/(Fe + Mg)) in garnet, biotite and cordierite is observed from patch migmatites through schollen and stromatic migmatites to residual melanosomes. Whole‐rock compositions of patch, schollen and stromatic migmatites are similar to those of non‐migmatitic rocks from the surrounding area. These metasedimentary rocks are interpreted as the protoliths of the migmatites. A decrease in the silica content of migmatites from 63 to 40 wt% SiO₂ is accompanied by an increase in Al₂O₃ and MgO+FeO and by a depletion in alkalis. Thermodynamic modelling in the NCKFMASHTO system for the different types of migmatite provides peak metamorphic conditions ~7–8 kbar and 840 °C. A nearly isothermal decompression history down to 5.5 kbar was followed by isobaric cooling from 840 °C through 690 °C to lower temperatures. The preservation of granulite facies assemblages and the variation in mineral assemblages and chemical composition can be modelled by ongoing H₂O‐fluxed melting accompanied by melt loss. The fluids were probably released by the crystallizing gabbro–diorite, infiltrating the metasedimentary rocks and fluxing melting. Release of fluids and melt loss were probably favoured by coeval deformation (D2). The amount of melt remaining in the system varied considerably among the different types of migmatite. The whole‐rock compositions of the samples, the modelled compositions of melts at the solidus at 5.5 kbar and the residues show a good correlation.     

P–T–fluid evolution in the Mahalapye Complex, Limpopo high-grade terrane, eastern Botswana

Metapelites, migmatites and granites from the c. 2 Ga Mahalapye Complex have been studied for determining the P–T–fluid influence on mineral assemblages and local equilibrium compositions in the rocks from the extreme southwestern part of the Central Zone of the Limpopo high‐grade terrane in Botswana. It was found that fluid infiltration played a leading role in the formation of the rocks. This conclusion is based on both well‐developed textures inferred to record metasomatic reactions, such as Bt ? And + Qtz + (K₂O) and Bt ± Qtz ? Sil + Kfs + Ms ± Pl, and zonation of Ms | Bt + Qtz | And + Qtz and Grt | Crd | Pl | Kfs + Qtz reflecting a perfect mobility (Korzhinskii terminology) of some chemical components. The conclusion is also supported by the results of a fluid inclusion study. CO₂ and H₂O ( = 0.6) are the major components of the fluid. The fluid has been trapped synchronously along the retrograde P–T path. The P–T path was derived using mineral thermobarometry and a combination of mineral thermometry and fluid inclusion density data. The Mahalapye Complex experienced low‐pressure granulite facies metamorphism with a retrograde evolution from 770 °C and 5.5 kbar to 560 °C and 2 kbar, presumably at c. 2 Ga.     

Origin,age, and significance of deep‐seated granulite‐facies migmatites in the Barrow zones of Scotland,Cairn Leuchan,Glen Muick area

Petrological modelling of granulite‐facies mafic and semipelitic migmatites from Cairn Leuchan, northeast Scotland, has provided new constraints on the pressure (P) and temperature (T) conditions of high‐grade metamorphism in the type‐locality Barrow zones. Phase diagrams constructed in the Na₂O–CaO–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O–TiO₂–O₂ system have constrained the P?T conditions of peak metamorphism in the Glen Muick region of the upper sillimanite zone (Sill+Kfs) to have been at least ～840°C at ～9 kbar (high‐P granulite facies). These conditions are ～120°C and ～3 kbar higher than those recorded by lower sillimanite zone (Sill+Ms) units located only a few kilometres away to the southeast at Glen Girnock, indicating the presence of a significant thermal and barometric high exposed within the Scottish Dalradian, and supporting previous suppositions of a potential tectonic break between the two regions. U–Pb zircon geochronology performed on these mafic migmatites produced ages of c. 540–470 Ma from grains with both igneous and metamorphic morphological characteristics. Their basaltic protoliths likely formed during a period of volcanism dated at c. 570 Ma, associated with passive‐margin extension prior to the onset of Iapetus Ocean closure, and high‐grade metamorphism and partial melting is interpreted to have taken place at c. 470 Ma, synchronous with sillimanite‐grade metamorphism recorded elsewhere in the Dalradian. These high‐grade Cairn Leuchan lithologies are interpreted as representing a fragment of Grampian Terrane lower crust that was exhumed via displacement along a steeply dipping tectonic discontinuity related to the Portsoy–Duchray Hill Lineament, and are not pre‐Caledonian Mesoproterozoic basement, as suggested by some previous studies. Veins within some mafic migmatites in the Cairn Leuchan area, composed almost entirely (>80%) of garnet, with minor quartz, plagioclase, amphibole, and clinopyroxene, are interconnected with leucosomes and are interpreted to represent former garnet‐bearing melt segregations that have been locally drained of almost all melt. Thus, mafic components of the lower crust, currently underlying relatively lower grade metasediments exposed to the southeast, may represent a potential source rock for widely documented, post‐orogenic felsic plutons, sills, and dykes that occur throughout the Grampian Terrane.     

Decoding the complex internal chemical structure of garnet porphyroblasts from the Zermatt area,Western Alps

Garnet is a prototypical mineral in metamorphic rocks because it commonly preserves chemical and textural features that can be used for untangling its metamorphic development. Large garnet porphyroblasts may show extremely complex internal structures as a result of a polycyclic growth history, deformation, and modification of growth structures by intra‐ and intercrystalline diffusion. The complex internal structure of garnet porphyroblasts from garnet–phengite schists (GPS) of the Zermatt area (Western Alps) has been successfully decoded. The centimetre‐sized garnet porphyroblasts are composed of granulite facies garnet fragments overgrown by a younger generation of grossular‐rich eclogite facies garnet. The early granulite facies garnet (G‐Grt) formed from low‐P, high‐T metamorphism during a pre‐Alpine orogenic event. The late garnet (E‐Grt) is typical of high‐pressure, low‐temperature (HPLT) metamorphism and can be related to Alpine subduction of the schists. Thus, the garnet of the GPS are polycyclic (polymetamorphic). G‐Grt formation occurred at ~670 MPa and 780°C, E‐Grt formed at ~1.7 GPa and 530°C. The G‐Grt is relatively rich in Prp and poor in Grs, while E‐Grt is rich in Grs and poor in Prp. The Alm content (mol.%) of G‐Grt is 68 of E‐Grt 55. After formation of E‐Grt between and around fragmented G‐Grt at 530°C, the GPS have been further subducted and reached a maximum temperature of 580°C before exhumation started. Garnet composition profiles indicate that the initially very sharp contacts between the granulite facies fragments of G‐Grt and fracture seals of HPLT garnet (E‐Grt) have been modified by cation diffusion. The profiles suggest that Ca did not exchange at the scale of 1 µm, whereas Fe and Mg did efficiently diffuse at the derived maximum temperature of 580°C for the GPS at the scale of 7–8 µm. The Grt–Grt diffusion profiles resulted from spending c. 10 Ma at 530–580°C along the P–T–t path. The measured Grt composition profiles are consistent with diffusivities of log D_MgFe = ?25.8 m²/s from modelled diffusion profiles. Mg loss by diffusion from G‐Grt is compensated by Fe gain by diffusion from E‐Grt to maintain charge balance. This leads to a distinctive Fe concentration profile typical of uphill diffusion.     

Metamorphic evolution of the Río Santa Rosa Granulites,northern Sierra de Comechingones,Argentina

Highly anhydrous granulites from Río Santa Rosa in the eastern Sierras Pampeanas of Argentina occur as a thick lens surrounded by melt-depleted migmatites. Grt–Crd granulite composed of Qtz+Pl+Grt+Crd+Ilm±Spl±Ath±Phl is the dominant rock, whereas Opx–Grt granulite appears as discontinuous lenses in the center of the granulite body. Grt–Crd granulite includes blocks of metabasite that are relics of refractory lithologic beds interlayered in the supracrustal sequence. A distinct assemblage composed of Qtz, Pl, Grt, Crd, Opx, Spl, Crn, Sil, Bt, Phl, Ath, and Fe–Ti oxides in different combinations was generated in a reaction zone between Grt–Crd granulites and metabasites at peak metamorphism (850–900 °C and 7.6±0.5 kbar). The P–T trajectory of Grt–Crd granulites suggests an early prograde garnet-forming stage followed by nearly isothermal decompression that caused garnet breakdown. Melting and melt draining accompanying garnet growth was active during heating (to 900 °C) at intermediate pressures (∼7.6 kbar). Peak P–T estimates for Opx–Grt granulites are similar to those obtained with Grt–Crd granulites, which indicates that both granulites passed through the highest thermal stage. These results constrain the late evolution of Opx–Grt granulite to a garnet-consuming stage. Furthermore, they imply that garnet formation in Opx–Grt granulite happened at an early prograde P–T trajectory. Garnet growth in Opx–Grt granulite cannot result from heating at high pressure, which would lead to an apparent contradiction in the prograde P–T paths of the two granulites. This discrepancy may be solved by demonstrating that Opx–Grt granulite is the product of synmetamorphic mafic magmatism that was contaminated while cooling. The Río Santa Rosa granulites are inferred to have formed in a thickened crust in which mafic magmatic activity providing a local heat input.     

Upper‐amphibolite facies partial melting of paragneisses from the Epupa Complex,NW Namibia,and relations to Mesoproterozoic anorthosite magmatism

The evolution of the mineral assemblages and P–T conditions during partial melting of upper‐amphibolite facies paragneisses in the Orue Unit, Epupa Complex, NW Namibia, is modelled with calculated P–T–X phase diagrams in the Na₂O–CaO–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O system. The close concordance of predictions from the phase diagrams to petrographic observations and thermobarometric results documents that quantitative phase diagrams are suitable to explain the phase relationships in migmatitic upper‐amphibolite facies low‐ and medium‐pressure metapelites, which occur in many high‐grade metamorphic terranes worldwide. Different mineral assemblages in the migmatitic metapelites of the Orue Unit reflect regional discrepancies in the metamorphic grade: in a Northern Zone, early biotite–sillimanite–quartz assemblages were replaced via melt‐producing reactions by cordierite‐bearing assemblages. In a Southern Zone, they were replaced via melt‐producing reactions by garnet‐bearing assemblages while cordierite is restricted to rare metapelitic granofelses, which preserve Grt–Sil–Crd–Bt peak assemblages. Peak‐metamorphic conditions of 700–750 °C at 5.5–6.7 kbar in the Southern Zone and of ～750 °C at 4.5 kbar in the Northern Zone are estimated by integrating thermobarometric calculations with data from calculated mineral composition isopleths. Retrograde back‐reactions between restite and crystallizing melt are recorded by the replacement of garnet by biotite–sillimanite and/or biotite–muscovite intergrowths. Upper‐amphibolite facies metamorphism and partial melting (c. 1340–1320 Ma) in the rocks of the Southern Zone of the Orue Unit, which underwent probably near‐isobaric heating–cooling paths, are attributed to contact metamorphism induced by the coeval (c. 1385–1319 Ma) emplacement of the Kunene Intrusive Complex, a huge massif‐type anorthosite body. The lower‐pressure metapelites of the Northern Zone are interpreted to record contact metamorphism at an upper crustal level.     

Petrogenesis of garnet-bearing ultramafic rocks and associated eclogites in the Su-Lu ultrahigh-P metamorphic terrane, eastern China

Ultramafic blocks that themselves contain eclogite lenses in the Triassic Su-Lu ultrahigh-P terrane of eastern China range in size from hundreds of metres to kilometres. The ultramafic blocks are enclosed in quartzofeldspathic gneiss of early Proterozoic age. Ultramafic rocks include garnetiferous lherzolite, wehrlite, pyroxenite, and hornblende peridotite. Garnet lherzolites are relatively depleted in Al₂O₃ (<3.8wt%), CaO (<3.2%) and TiO₂ (<0.11 wt%), and are low in total REE contents (several p.p.m.), suggesting that the rocks are residual mantle material that was subjected to low degrees of partial melting. The eclogite lenses or layers within the ultramafic rocks are characterized by higher MgO and CaO, lower Al₂O₃ and TiO₂ contents, and a higher CaO/Al₂O₃ ratio compared to eclogites enclosed in the quartzofeldspathic gneiss. Scatter in the plots of major and trace elements vs. MgO, REE patterns and La, Sm and Lu contents suggest that some eclogites were derived from melts formed by various degrees (0.05–0.20) of partial melting of peridotite, and that other eclogites formed by accumulation of garnet and clinopyroxene ± trapped melt in the upper mantle. Both ultramafic and eclogitic rocks have experienced a complex metamorphic history. At least six stages of recrystallization occurred in the ultramafic rocks based on an analysis of reaction textures and mineral compositions. Stage I is a high temperature protolith assemblage of Ol + Opx + Cpx + Spl. Stage II consists of the ultrahigh-pressure assemblage Ol + Cpx + Opx + Grt. Stage III is manifested by the appearance of fine-grained garnet after coarse-grained garnet. Stage IV is characterized by formation of kelyphitic rims of fibrous Opx and Cpx around garnet, and replacement of garnet by spinel and pargasitic-hornblende. Stage V is represented by the assemblage Ol + Opx + Prg-Hbl + Spl. The mineral assemblages of stages VI_A and VI_B are Ol + Tr-Amp + Chl and Serp + Chl ± talc, respectively. Garnet and orthopyroxene all show a decrease in MgO with retrogressive recrystallization and Na₂O in clinopyroxene also decreases throughout this history. Eclogites enclosed within ultramafic blocks consist of Grt + Omp + Rt ± Qtz ± Phn. A few quartz-bearing eclogites contain rounded and oval inclusion of polycrystalline quartz aggregates after coesite in garnet and omphacite. Minor retrograde features include thin symplectic rims or secondary amphiboles after Cpx, and ilmenite after rutile. P-T estimates indicate that the ultrahigh-metamorphism (stage II) of ultramafic rocks occurred at 820-900d? C and 36-41 kbar and that peak metamorphism of eclogites occurred at 730-900d? C and >28 kbar. Consonant with earlier plate tectonic models, we suggest that these rocks were underplated at the base of the continental crust. The rocks then underwent ultrahigh-pressure metamorphism and were tectonically emplaced into thickened continental crust during the Triassic collision between the Sino-Korean and Yangtze cratons.     

Polymetamorphic history of a relict Permian hornfels from the central Gran Paradiso Massif (Western Alps,Italy): a microstructural and thermodynamic modelling study

A petrological and thermobarometric study of the Lago Teleccio hornfelses was undertaken to reconstruct the polymetamorphic evolution and constrain the P–T conditions of Permian contact metamorphism. The Lago Teleccio metasedimentary rocks record a Variscan regional metamorphism characterized by amphibolite facies mineral assemblages including quartz, plagioclase, K‐feldspar (Kfs 1), biotite, garnet (Grt 1) and staurolite; this was followed by a late‐Variscan mylonitization event. Metamorphism of the Variscan metamorphic rocks at the contact with a Permian granitic intrusion produced static recrystallization and/or new growth of quartz, garnet (Grt 2), plagioclase, K‐feldspar (Kfs 2), cordierite, green spinel, biotite and prismatic sillimanite (Contact 1). This thermal event, which occurred at a peak pressure of 0.23–0.35 GPa, temperature of 670–700 °C and a_H2O of 0.75–1, was followed either during post‐contact metamorphism cooling or, more likely, during the early‐Alpine metamorphism by the breakdown of cordierite into an anhydrous kyanite + orthopyroxene + quartz assemblage. The poorly developed early‐Alpine eclogite facies metamorphism (Alpine 1) was characterized by relatively anhydrous mineral associations and low strain, which locally produced coronitic and pseudomorphous microstructures in metasedimentary rocks, with scanty formation of jadeite, zoisite and a new high‐pressure garnet (Grt 3). Greenschist facies retrogression (Alpine 2) was characterized by the local development of a chlorite‐ and muscovite‐bearing mineral association, suggestive of aqueous fluid incursion. In the hornfelses, the limited extent of metamorphic overprinting is suggested by the fine grain size of the Alpine mineral associations, which formed at the expense of the Permian contact metamorphic associations, and was favoured by the anhydrous mineralogy of the hornfelses.     

Amphibolite to granulite transition in aluminous greywackes from the Sierra de Comechingones, Córdoba, Argentina

We discuss upper-amphibolite to granulite facies, early Palaeozoic metamorphism and partial melting of aluminous greywackes from the Sierra de Comechingones, SE Sierras Pampeanas of Central Argentina. Consistent P–T estimates, obtained from equilibria involving Al and Ti exchange components in biotite and from more traditional thermobarometric equilibria, suggest that peak metamorphism of the exposed section took place at an essentially constant pressure of 7–8 kbar, and at temperatures ranging from 650 to 950 °C. Mineral compositions record an initial decompression, after peak metamorphism, of c. 1.5 kbar, which was accompanied by a cooling of c. 100 °C. Upper-amphibolite facies gneisses consist of the assemblage Qtz+Pl+Bt+Grt+Rt/Ilm. The transition to the granulite facies is marked by the simultaneous appearance of the assemblage Kfs+Sil and of migmatitic structures, suggesting that the amphibolite to granulite transition in the Sierra de Comechingones corresponds to the beginning of melting. Rocks with structural and/or chemical manifestations of partial melting range from metatexites, to diatexites, to melt-depleted granulites, consisting of the assemblage Grt+Crd+Pl+Qtz+Ilm±Ath. The melting stage overlapped at least partially with decompression, as suggested by the occurrence of cordierite, in both the migmatites and the residual granulites, of two distinct textural types: idiomorphic porphyroblasts (probably representing peritectic cordierite) and garnet-rimming coronas. Metapelitic rocks are unknown in the Sierra de Comechingones. Therefore, it appears most likely that the Al-rich residual assemblages found in the migmatites and residual granulites were formed by partial melting of muscovite- and sillimanite-undersaturated metagreywackes. We propose a mechanism for this that relies on the sub-solidus stabilization of garnet and the ensuing changes in the octahedral Al content of biotite with pressure and temperature.     

Deep subduction of mantle-derived garnet peridotites from the Su-Lu UHP metamorphic terrane in China

Garnet peridotites from the southern Su‐Lu ultra‐high‐pressure metamorphic (UHPM) terrane, eastern China, contain porphyroblastic garnet with aligned inclusions comprising a low‐P–T mineral assemblage (chlorite, hornblende, Na‐gedrite, Na‐phlogopite, talc, spinel and pyrite). Orthopyroxene porphyroblasts show fine exsolution lamellae of clinopyroxene and minor chromite. A clinopyroxene inclusion in garnet shows some orthopyroxene exsolution lamellae. Both the rims of porphyroblastic pyroxene and garnet and the matrix pyroxene and garnet crystallized at the expense of olivine. This is interpreted as a result of metasomatism of the peridotites by an SiO₂‐rich melt at UHP conditions. A chromian garnet further overgrew on the rims of the garnet. The X_Mg values (Mg/(Mg+Fe)) of porphyroblastic garnet decrease from core to rim and vary in different peridotite samples, while the compositions of both the porphyroblastic and the matrix pyroxene are similar in terms of Ca–Mg–Fe. The Mg‐rich cores of porphyroblastic garnet and orthopyroxene record high temperatures and pressures (c. 1000 °C, ≥5.1 GPa), whereas the matrix minerals, including the rims of porphyroblasts, record much lower P–T (c. 4.2 GPa, c. 760 °C). Sm–Nd data give apparent isochron ages of c. 380 Ma and negative ε_Nd(0) values (c.?9). These dates are considered meaningless due to isotopic disequilibrium between garnet cores and the rest of the rocks. The isotopic disequilibrium was probably caused by metasomatism of the peridotites by melt/fluids derived from the coevally subducted crustal materials. On the other hand, the Rb–Sr isotopic systems of phlogopite and clinopyroxene appear to have reached equilibrium and record a cooling age of c. 205 Ma. It is suggested that the garnet peridotites were originally emplaced into a low‐P–T environment prior to the c. 220 Ma continental collision, during which they were subducted together with crustal rocks to mantle depth and subjected to UHP metamorphism. An important corollary is that at least some of the coevally subducted crustal rocks in the Su‐Lu terrane have been subjected to peak metamorphism at P–T conditions much higher than presently estimated (≥2.7 GPa, ≤800 °C).     

Petrogenesis of the garnet peridotite and garnet-free peridotite of the Zhimafang ultramafic body in the Sulu ultrahigh-pressure metamorphic belt, eastern China

The CCSD‐PP1 drillhole penetrated a 110‐m‐thick sequence of the Zhimafang ultramafic body in the Sulu ultrahigh‐pressure (UHP) metamorphic belt, east China. The sequence consists of interlayered garnet‐bearing (Grt) and garnet‐free (GF) peridotite. Eleven layers of Grt‐peridotite, ranging from 1.2 to 9.5 m in thickness, have an aggregate thickness of 54.49 m, whereas eight layers of GF‐peridotite, ranging from 2.2 to 14.2 m in thickness, have a total thickness of 57.53 m. The boundaries between the two rock types are gradational. The Grt‐peridotites have slightly higher contents of Al₂O₃, CaO and SiO₂, and lower Mg^#s (0.90–0.92) than the GF‐peridotites (Mg^#s 0.91–0.93). Both contain low TiO₂ (<0.05 wt%) and have higher modal abundances of enstatite (average 10 vol.%) than diopside (1–5 vol.%), typical of depleted‐type upper mantle. The diopside in these rocks has high and relatively uniform Mg^# members (0.93–0.95), but highly variable Al₂O₃ (0.2–2.3 wt%), Na₂O (0.5–2.5 wt%) and Cr₂O₃ (0.38–2.09 wt%). Enstatite (En_92?93) contains very low Al₂O₃ (0–0.3 wt%). Both porphyroblastic and equigranular garnet are present. The equigranular varieties are zoned, from core to rim in Cr₂O₃ (3.4–4.2 wt%), MgO (18.4–17.5 wt%) and Al₂O₃ (21.1–20.1 wt%). Titania is very low in all the garnet, mostly <0.05 wt%. Chromite or chromium (Cr)‐spinel occur both in the Grt‐ and GF‐peridotite, and are characterized by high contents of Cr₂O₃ (49–58 wt%) and FeO (24–43 wt%), similar to that in iron‐rich Alpine‐type peridotites. Based on the bulk‐rock MgO–FeO compositions, the Zhimafang Grt‐peridotite probably underwent 20–30% partial melting, whereas the GF‐peridotite may have undergone as much as 35–40% partial melting, suggesting that the two rock types owe their differences to different degrees of partial melting rather than to pressure differences during metamorphism.     

Phase equilibria modelling of residual migmatites and granulites: An evaluation of the melt‐reintegration approach

Suprasolidus continental crust is prone to loss and redistribution of anatectic melt to shallow crustal levels. These processes ultimately lead to differentiation of the continental crust. The majority of granulite facies rocks worldwide has experienced melt loss and the reintegration of melt is becoming an increasingly popular approach to reconstruct the prograde history of melt‐depleted rocks by means of phase equilibria modelling. It involves the stepwise down‐temperature reintegration of a certain amount of melt into the residual bulk composition along an inferred P–T path, and various ways of calculating and reintegrating melt compositions have been developed and applied. Here different melt‐reintegration approaches are tested using El Hoyazo granulitic enclaves (SE Spain), and Mt. Stafford residual migmatites (central Australia). Various sets of P–T pseudosections were constructed progressing step by step, to lower temperatures along the inferred P–T paths. Melt‐reintegration was done following one‐step and multi‐step procedures proposed in the literature. For El Hoyazo granulites, modelling was also performed reintegrating the measured melt inclusions and matrix glass compositions and considering the melt amounts inferred by mass–balance calculations. The overall topology of phase diagrams is pretty similar, suggesting that, in spite of the different methods adopted, reintegrating a certain amount of melt can be sufficient to reconstruct a plausible prograde history (i.e. melting conditions and reactions, and melt productivity) of residual migmatites and granulites. However, significant underestimations of melt productivity may occur and have to be taken into account when a melt‐reintegration approach is applied to highly residual (SiO₂ <55 wt%) rocks, or to rocks for which H₂O retention from subsolidus conditions is high (such as in the case of rapid crustal melting triggered by mafic magma underplating).     

Origin of CO2-rich fluid inclusions in leucosomes from the Skagit migmatites, North Cascades, Washington, USA

CO₂–CH₄ fluid inclusions are present in anatectic layer-parallel leucosomes from graphite-bearing metasedimentary rocks in the Skagit migmatite complex, North Cascades, Washington. Petrological evidence and additional fluid inclusion observations indicate, however, that the Skagit Gneiss was infiltrated by a water-rich fluid during high-temperature metamorphism and migmatization. CO₂-rich fluid inclusions have not been observed in Skagit metasedimentary mesosomes or melanosomes, meta-igneous migmatites, or unmigmatized rocks, and are absent from subsolidus leucosomes in metasedimentary migmatites. The observation that CO₂-rich inclusions are present only in leucosomes interpreted to be anatectic based on independent mineralogical and chemical criteria suggests that their formation is related to migmatization by partial melting. Although some post-entrapment modification of fluid inclusion composition may have occurred during decompression and deformation, the generation of the CO₂-rich fluid is attributed to water-saturated partial melting of graphitic metasedimentary rocks by a reaction such as biotite + plagioclase + quartz + graphite ± Al₂SiO₅+ water-rich fluid = garnet + melt + CO₂–CH₄. The presence of CO₂-rich fluid inclusions in leucosomes may therefore be an indication that these leucosomes formed by anatexis. Based on the inferences that (1) an influx of fluid triggered partial melting, and (2) some episodes of fluid inclusion trapping are related to migmatization by anatexis, it is concluded that a free fluid was present at some time during high-temperature metamorphism. The infiltrating fluid was a water-rich fluid that may have been derived from nearby crystallizing plutons. Because partial melting took place at pressures of at least 5 kbar, abundant free fluid may have been present in the crust during orogenesis at depths of at least 15 km.     

MnNCKFMASH phase relations in cordierite-orthopyroxene migmatitic gneisses, southern india: implications for low-pressure crustal melting under granulite-facies

Cordierite-orthopyroxene migmatitic gneisses exposed in Achankovil unit of the Kerala Khondalite Belt, southern India show evidences of melting, melt extraction and in-situ crystallization of melt under granulite-facies conditions. The sequential mineral assemblages garnet + biotite + orthopyroxene + plagioclase + quartz (± melt) in the mesosomes and garnet + biotite + orthopyroxene + cordierite + plagioclase + K-feldspar + quartz + melt in the melanosomes makes the Achankovil cordierite-orthopyroxene migmatitic gneisses a good example of anatectic rocks, where substantial melt fractions remained in-situ during decompression and cooling. Therefore, the rocks provide an opportunity to investigate deep crustal processes and record of rheological (thermal and mechanical) reequilibration prevailed during the final stages of orogeny. The significance of cordierite formation and its possible relationship with melt formation are investigated applying theoretical calculations in the MnO-Na₂O-CaO-K₂O-FeO-MgO-Al₂O₃-SiO₂-H₂O (MnNCKFMASH) system. Results of numerical modelling of the mineral assemblages in pressure-temperature-composition (P-T-X) pseudosections using Perple_X infer that the sequence of reactions involving formation of cordierite-orthopyroxene-melt assemblage is consistent with an isothermal decompression (with a pressure drop of >1.5 kbars) at high temperatures (>800 °C), forming leucosomes. Biotite dehydration melting reactions, occurring above 4.5 kbars constrain prograde arm of the P-T trajectory and is interpreted as a product of crustal thickening, which was followed by rapid decompression. The final stage of exhumation is characterized by rehydration of cordierites in the melanosome by melt-solid interactions at exceptionally low-pressure (??3.2 kbars) conditions. The high-temperature isothermal decompression inferred from the mineral reactions and P-T-X pseudosections constitute a clockwise P-T path for the exhumation of the lower crust. This clockwise P-T path is consistent with the common tectonic model accepted for the genesis of granulite-facies migmatites during crustal thickening and later unroofing, accompanied with arc-continent collision. Our conclusions indicate low-P metamorphism and anatexis can be traced to convergent setting, where melt buoyancy considerably decreases density of the lithosphere and modifies rheology leading to rapid exhumation of the lower crust. Therefore, the crustal evolution in the Kerala Khondalite Belt is correlated with two stage processes: (i) thickening of the crust in relation to a continental-arc setting, followed by (ii) exhumation along a high-temperature stable geotherm with sufficient pressure release associated with syn- to post-convergence transpression and transtension.     

Dating metamorphic reactions and fluid flow: application to exhumation of high-P granulites in a crustal-scale shear zone, western Canadian Shield

The Legs Lake shear zone is a crustal‐scale thrust fault system in the western Canadian Shield that juxtaposes high‐pressure (1.0+ GPa) granulite facies rocks against shallow crustal (< 0.5 GPa) amphibolite facies rocks. Hangingwall decompression is characterized by breakdown of the peak assemblage Grt + Sil + Kfs + Pl + Qtz into the assemblage Grt + Crd + Bt ± Sil + Pl + Qtz. Similar felsic granulite occurs throughout the region, but retrograde cordierite is restricted to the immediate hangingwall of the shear zone. Textural observations, petrological analysis using P–T/P–M_H2O phase diagram sections, and in situ electron microprobe monazite geochronology suggest that decompression from peak conditions of 1.1 GPa, c. 800 °C involved several distinct stages under first dry and then hydrated conditions. Retrograde re‐equilibration occurred at 0.5–0.4 GPa, 550–650 °C. Morphology, X‐ray maps, and microprobe dates indicate several distinct monazite generations. Populations 1 and 2 are relatively high yttrium (Y) monazite that grew at 2.55–2.50 Ga and correspond to an early granulite facies event. Population 3 represents episodic growth of low Y monazite between 2.50 and 2.15 Ga whose general significance is still unclear. Population 4 reflects low Y monazite growth at 1.9 Ga, which corresponds to the youngest period of high‐pressure metamorphism. Finally, population 5 is restricted to the hydrous retrograded granulite and represents high Y monazite growth at 1.85 Ga that is linked directly to the synkinematic garnet‐consuming hydration reaction (KFMASH): Grt + Kfs + H₂O = Bt + Sil + Qtz. Two samples yield weighted mean microprobe dates for this population of 1853 ± 15 and 1851 ± 9 Ma, respectively. Subsequent xenotime growth correlates with the reaction: Grt + Sil + Qtz + H₂O = Crd. We suggest that the shear zone acted as a channel for fluid produced by dehydration of metasediments in the underthrust domain.     

Orogeny, migmatites and leucogranites: A review

The type ofP-T-t path and availability of fluid (H₂O-rich metamorphic volatile phase or melt) are important variables in metamorphism. Collisional orogens are characterized by clockwiseP-T evolution, which means that in the core, where temperatures exceed the wet solidus for common crustal rocks, melt may be present throughout a significant portion of the evolution. Field observations of eroded orogens show that lower crust is migmatitic, and geophysical observations have been interpreted to suggest the presence of melt in active orogens. A consequence of these results is that orogenic collapse in mature orogens may be controlled by a partially-molten layer that decouples weak crust from subducting lithosphere, and such a weak layer may enable exhumation of deeply buried crust. Migmatites provide a record of melt segregation in partially molten crustal materials and syn-anatectic deformation under natural conditions. Grain boundary flow and intra-and inter-grain fracture flow are the principal grain scale melt flow mechanisms. Field observations of migmatites in ancient orogens show that leucosomes occur oriented in the metamorphic fabrics or are located in dilational sites. These observations are interpreted to suggest that melt segregation and extraction are syntectonic processes, and that melt migration pathways commonly relate to rock fabrics and structures. Thus, leucosomes in depleted migmatites record the remnant permeability network, but evolution of permeability networks and amplification of anomalies are poorly understood. Deformation of partially molten rocks is accommodated by melt-enhanced granular flow, and volumetric strain is accommodated by melt loss. Melt segregation and extraction may be cyclic or continuous, depending on the level of applied differential stress and rate of melt pressure buildup. During clockwiseP-T evolution, H₂O is transferred from protolith to melt as rocks cross dehydration melting reactions, and H₂O may be evolved above the solidus at lowP by crossing supra-solidus decompression-dehydration reactions if micas are still present in the depleted protolith. H₂O dissolved in melt is transported through the crust to be exsolved on crystallization. This recycled H₂O may promote wet melting at supra-solidus conditions and retrogression at subsolidus conditions. The common growth of ‘late’ muscovite over sillimanite in migmatite may be the result of this process, and influx of exogenous H₂O may not be necessary. However, in general, metasomatism in the evolution of the crust remains a contentious issue. Processes in the lower-most crust may be inferred from studies of xenolith suites brought to the surface in lavas. Based on geochemical data, we can use statistical methods and modeling to evaluate whether migmatites are sources or feeder zones for granites, or simply segregated melt that was stagnant in residue, and to compare xenoliths of inferred lower crust with exposed deep crust. Upper-crustal granites are a necessary complement to melt-depleted granulites common in the lower crust, but the role of mafic magma in crustal melting remains uncertain. Plutons occur at various depths above and below the brittle-to-viscous transition in the crust and have a variety of 3-D shapes that may vary systematically with depth. The switch from ascent to emplacement may be caused by amplification of instabilities within (permeability, magma flow rate) or surrounding (strength or state of stress) the ascent column, or by the ascending magma intersecting some discontinuity in the crust that enables horizontal magma emplacement followed by thickening during pluton inflation. Feedback relations between rates of pluton filling, magma ascent and melt extraction maintain compatibility among these processes.     

Stability of sapphirine + quartz in the oxidized rocks of the Wilson Lake terrane,Labrador: calculated equilibria in NCKFMASHTO

The equilibrium coexistence of sapphirine + quartz is inferred to record temperatures in excess of 980 °C, based on the stability of this assemblage in the simplified chemical system FeO–MgO–Al₂O₃–SiO₂ (FMAS) system. However, the potential for sapphirine to contain significant Fe³⁺ suggests that the stability of sapphirine + quartz could extend to lower temperatures than those constrained in this ideal system. The Wilson Lake terrane in the Grenville Province of central Labrador preserves sapphirine + quartz‐bearing assemblages in highly oxidized bulk compositions, and provides an opportunity to explore the stability of sapphirine + quartz in such rock compositions within the Na₂O–CaO–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O–TiO₂–O (NCKFMASHTO) chemical system. Starting with the phase equilibria in FeO–MgO–Al₂O₃–SiO₂–TiO₂–O (FMASTO), expansion into K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O–TiO₂–O (KFMASHTO) allows the effect of the stability of the additional phases, biotite, K‐feldspar and melt, on the stability of sapphirine + quartz to be assessed. These phase relations are evaluated generally using P–T projections, and the ultimate extension into NCKFMASHTO is done with pseudosections. Conditions of peak metamorphism in the Wilson Lake terrane are constrained using P–T pseudosections, and the appropriate H₂O and O contents to use in the modelled compositions are investigated using T–M_H2O and T–M_O pseudosections. The peak P–T estimates from a sapphirine + quartz‐bearing sample are ～960 to 935 °C at ～10 to 8.6 kbar, similar to estimates from orthopyroxene + sillimanite + quartz ± garnet‐bearing samples. Whereas the sapphirine + quartz‐bearing sample is more Fe‐rich than the orthopyroxene + sillimanite‐bearing sample on an all‐Fe‐as‐FeO basis, once the oxidation state is taken into account, the former is effectively more magnesian than the latter, accounting for the sapphirine occurrence.