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The petrology and timing of crustal melting has been investigated in the migmatites of the Higher Himalayan Crystalline (HHC) exposed in Sikkim, India. The metapelites underwent pervasive partial melting through hydrous as well as dehydration melting reactions involving muscovite and biotite to produce a main assemblage of quartz, K-feldspar, plagioclase, biotite, garnet ± sillimanite. Peak metamorphic conditions were 8–9 kbar and ~800 °C. Monazite and zircon crystals in several migmatites collected along a N–S transect show multiple growth domains. The domains were analyzed by microbeam techniques for age (SHRIMP) and trace element composition (LA-ICP-MS) to relate ages to conditions of formation. Monazite preserves the best record of metamorphism with domains that have different zoning pattern, composition and age. Zircon was generally less reactive than monazite, with metamorphic growth zones preserved in only a few samples. The growth of accessory minerals in the presence of melt was episodic in the interval between 31 and 17 Ma, but widespread and diachronous across samples. Systematic variations in the chemical composition of the dated mineral zones (HREE content and negative Eu anomaly) are related to the variation in garnet and K-feldspar abundances, respectively, and thus to metamorphic reactions and P–T stages. In turn, this allows prograde versus decompressional and retrograde melt production to be timed. A hierarchy of timescales characterizes melting which occurred over a period of ~15 Ma (31–17 Ma): a given block within this region traversed the field of melting in 5–7 Ma, whereas individual melting reactions lasted for time durations below, or approaching, the resolution of microbeam dating techniques (~0.6 Ma). An older ~36 Ma high-grade event is recorded in an allocthonous relict related to mafic lenses. We identify two sections of the HHC in Sikkim that traversed similar P–T conditions at different times, separated by a tectonic discontinuity. The higher structural levels reached melting and peak conditions later (~26–23 Ma) than the lower structural levels (~31–27 Ma). Diachronicity across the HHC cannot be reconciled with channel flow models in their simplest form, as it requires two similar high-grade sections to move independently during collision.

Dehydration reactions in the subducting slab liberate fluids causing major changes in rock density, volume and permeability. Although it is well known that the fluids can migrate and interact with the surrounding rocks, fluid pathways remain challenging to track and the consequences of fluid-rock interaction processes are often overlooked. In this study, we investigate pervasive fluid-rock interaction in a sequence of schists and mafic felses exposed in the Theodul Glacier Unit (TGU), Western Alps. This unit is embedded within metaophiolites of the Zermatt-Saas Zone and reached eclogite-facies conditions during Alpine convergence. Chemical mapping and in situ oxygen isotope analyses of garnet from the schists reveal a sharp chemical zoning between a xenomorphic core and a euhedral rim, associated to a drop of ~ 8‰ in δ18O. Thermodynamic and δ18O models show that the large amount of low δ18O H2O required to change the reactive bulk δ18O composition cannot be produced by dehydration of the mafic fels from the TGU only, and requires a large contribution of the surrounding serpentinites. The calculated time-integrated fluid flux across the TGU rocks is 1.1 × 105 cm3/cm2, which is above the open-system behaviour threshold and argues for pervasive fluid flow at kilometre-scale under high-pressure conditions. The transient rock volume variations caused by lawsonite breakdown is identified as a possible trigger for the pervasive fluid influx. The calculated schist permeability at eclogite-facies conditions (~ 2 × 10–20 m2) is comparable to the permeability determined experimentally for blueschist and serpentinites.

Garnet is one of the most robust and ubiquitous minerals that record element zoning during crustal metamorphism. In addition to major elements, zoning in trace elements can provide a wealth of information to document the changing conditions of garnet growth and modification. However, mapping trace elements at low concentrations, over large areas and with high resolution has remained a major challenge. We present a comprehensive investigation of the TE distribution in garnet from three Alpine samples that underwent a complex evolution at different metamorphic conditions. The TE distribution in garnet grains is mapped in 2D in thin section with a novel approach using laser ablation inductively coupled plasma time of flight mass spectrometry (LA-ICP-TOFMS) to achieve a lateral resolution of 5 µm and limits of detection for the heavy rare earth elements (REE) down to 0.2 µg/g. Comparison with major element zoning measured by electron probe microanalysis and trace elements measured by conventional LA-ICPMS spot analysis testifies to the accuracy of the measurements. Garnet in an amphibolite-facies metapelite from Campolungo, Central Alps, that recorded metamorphism to 600 °C preserves Y + REE trace element zoning that closely matches that of Ca. In this sample, there is no notable diffusive modification for trace elements. Y + REE zoning is dominated by Rayleigh fractionation in the core and by the sporadic breakdown of accessory phases producing annuli in the rim of the garnet. A granulite-facies garnet from Malenco, Eastern Central Alps, formed during subsolidus heating, followed by peritectic melting reactions up to temperatures of 800–850 °C. Major and trace element zoning are decoupled indicating diffusional resetting of major elements, whereas trace elements still largely document the growth history. Enrichment of trace elements in the garnet mantle may be related to the consumption of biotite (V, Cr) and the dissolution of zircon (Zr) and monazite (Y + REE) in the melt. Diffusion of Y + HREE at the core–mantle boundary occurred over a length scale of ~ 200 µm. Garnet in an eclogite from the Sesia Zone, Western Alps (P ~ 2 GPa, T ~ 600 °C), displays pronounced fluid-related veinlets, visible in FeO, MgO and MnO, which cross-cut the primary growth zoning. Surprisingly, complex Y + REE and Cr zoning is not affected by the veinlets, indicating that they did not form by a crack-seal mechanism but are rather related to a selective replacement process. The trace element maps provide a detailed insight into the growth and modification of garnet and thus allow assessment of equilibrium versus disequilibrium processes, and assist in determination of P–T conditions, garnet dating, diffusion modelling as well as documenting fluid-induced modifications.

This study investigates the behaviour of the Zr-in-rutile and Ti-in-zircon thermometers in granulite facies metapelites from the Ivrea-Verbano Zone lower crustal section. U–Pb ages of zircon constrain the timing of regional amphibolite–granulite facies metamorphism to 316 ± 3 Ma and record zircon recrystallisation and resetting of U–Pb ages at 276 ± 4 Ma and 258 ± 3 Ma. Zr-in-rutile thermometry records peak contact metamorphic temperatures related to intrusion of mafic magmatic rocks and gives peak temperatures between 900–930 °C and 1,000–1,020 °C that are consistent with the geological settings of the samples. Ti-in-zircon temperatures of 700–800 °C and 810–870 °C record growth or re-equilibration of zircon after cooling from peak temperatures. Ti-in-quartz thermometry for one sample records both peak and retrograde temperatures. Some rutiles in all samples record resetting of Zr-in-rutile temperatures at ~750–800 °C. Electron microprobe profiles across individual rutiles demonstrate that Zr expulsion occurred by recrystallisation rather than by diffusive exchange. Exsolution of small needles of baddelyite or zircon from rutile is an important method of Zr redistribution, but results in no net Zr loss from the grain. The demonstration that Zr-in-rutile thermometry can robustly record peak temperatures that are not recorded by any other thermometer emphasises the relevance of this technique to investigating the evolution of high-grade metamorphic terranes, such as those that characterise the lower crust.

A series of sharp bends (oroclines) are recognized in the Paleozoic to early Mesozoic New England Orogen of eastern Australia. The exact geometry and origin of these bends is obscured by voluminous magmatism and is still debated. Here we present zircon U‐Pb ages that confirm the lateral continuation of early Permian (296–288 Ma) granitoids and shed new light on the oroclinal structure. Orogenic curvature is defined by the alignment of early Permian granitoids parallel to the structural grain of the orogen, as well as the curved geometry of sub‐vertical deformation fabrics, forearc basin terranes, and serpentinite outcrops. Alternative geometrical interpretations may involve two bends (Texas and Coffs Harbour Oroclines), three bends (+Manning Orocline), or even four bends (+Nambucca Orocline). We argue that the model involving four bends is most consistent with available data, although further kinematic constraints are required to confirm the existence of the Manning and Nambucca Oroclines. A subsequent phase of younger magmatism (<260 Ma) cuts across the curved structural grain, providing a minimum age constraint for orocline development. Assuming a structure of four oroclines, we suggest a tentative tectonic model that involves an early stage of subduction curvature during slab rollback at 300–285 Ma, followed by bending associated with dextral transpression. A final tightening of the curved structures was possibly obtained by E‐W shortening during the late Permian to Triassic (265–230 Ma) Hunter‐Bowen orogeny. Key Points A strongly contorted orogen is recognized in the southern New England Orogen The curved geometry is outlined by the shape of Early Permian granitoids Oroclinal bending was possibly promoted by subduction rollback

The timing and dynamics of fluid-induced melting in the typical Barrovian sequence of the Central Alps has been investigated using zircon chronology and trace element composition. Multiple zircon domains in leucosomes and country rocks yield U–Pb ages spanning from ~32 to 22 Ma. The zircon formed during Alpine melting can be distinguished from the inherited and detrital cores on the basis of their age, Th/U (<0.1) and trace element composition. Ti-in-zircon thermometry indicates crystallization temperatures around 620–700°C. Their composition allows discriminating between (1) zircon formation in the presence of early garnet, (2) zircon in equilibrium with abundant L-MREE-rich accessory phases (allanite, titanite and apatite) typical of metatonalites, and (3) zircon formed during melting of metasediments in feldspar-dominated assemblages. The distribution of zircon overgrowths and ages indicate that repeated melting events occurred within a single Barrovian metamorphic cycle at roughly constant temperature; that in the country rocks zircon formation was limited to the initial stages of melting, whereas further melting concentrated in the segregated leucosomes; that melting occurred at different times in samples a few meters apart because of the local rock composition and localized influx of the fluids; and that leucosomes were repeatedly melted when fluids became available. The geochronological data force a revision of the temperature–time path of the migmatite belt in the Central Alps. Protracted melting over 10 My followed the fast exhumation of Alpine eclogites contained within the same region and preceded fast cooling in the order of 100°C/Ma to upper crustal levels.

Subduction zones represent one of the most critical settings for fluid recycling as a consequence of dehydration of the subducting lithosphere. A better understanding of fluid flows within and out of the subducting slab is fundamental to unravel the role of fluids during burial. In this study, major and trace element geochemistry combined with oxygen isotopes were used to investigate metasediments and eclogites from the Sesia Zone in order to reconstruct the effect of internal and external fluid pulses in a subducted continental margin. Garnet shows a variety of textures requiring dissolution–precipitation processes in presence of fluids. In polycyclic metasediments, garnet preserves a partly resorbed core, related to pre-Alpine high-temperature/low-pressure metamorphism, and one or multiple rim generations, associated with Alpine subduction metamorphism. In eclogites, garnet chemical zoning indicates monocyclic growth with no shift in oxygen isotopes from core to rim. In metasediments, pre-Alpine garnet relics show δ18O values up to 5.3 ‰ higher than the Alpine rims, while no significant variation is observed among different Alpine garnet generations within each sample. This suggests that an extensive re-equilibration with an externally-derived fluid of distinct lower δ18O occurred before, or in correspondence to, the first Alpine garnet growth, while subsequent influxes of fluid had δ18O close to equilibrium. The observed shift in garnet δ18O is attributed to a possible combination of (1) interaction with sea-water derived fluids during pre-Alpine crustal extension and (2) fluids from dehydration reactions occurring during subduction of previously hydrated rocks, such as the serpentinised lithospheric mantle or hydrated portions of the basement.

The structural and chemical properties of zircon inclusions in garnet megablasts from the Dora Maira Massif (Western Alps, Italy) were characterized in detail using charge contrast imaging, Raman spectroscopy, and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). The aim of this work is to determine to what extent the degree of metamictization, metamorphic recrystallization, inherent structural heterogeneity, chemical composition, and zoning, along with the elastic stress imposed by the host mineral, can influence the Raman peak position of the zircon inclusion and hence, the residual pressure estimated via Raman geo-thermobarometry. We show and confirm that metamictization and inherent structural heterogeneity have a major influence in the Raman spectra of zircon in terms of peak position and peak width. We suggest that, for spectral resolution of 2 cm , the peak width of the B mode near 1008 cm of reliable grains must be smaller than 5 cm . The method can be applied to both inherited igneous and newly formed Alpine metamorphic crystals. By coupling structural and chemical information, we demonstrate that there are no significant diferences between the Raman spectra of zircon with oscillatory-zoned texture, formed during magmatic crystallization, and those formed by fluid-induced Alpine (re)crystallization. The discrimination between magmatic and metamorphic zircon based only on micro-textural constraints is not robust. Finally, our results allow establishing a protocol devoted to the selection of reliable buried zircon inclusions, relying only on Raman spectroscopic measurements, to use for elastic thermobarometry applications.

High-pressure metamorphic rocks form during subduction of Earth’s crust to mantle depths at convergent plate margins. Their exposure at the surface of Earth today provides a record of the subduction zone process. In general, such metamorphic rocks record only a single cycle of subduction and exhumation, yet tectonic models suggest that individual rock units should undergo multiple subduction–exhumation cycles. Here we investigate the microstructure and chemical composition of metamorphic minerals in high-pressure rocks exposed in the Sesia zone in the Italian Western Alps. We find that the minerals white mica, garnet, allanite and zircon each exhibit multiple generations of mineral overgrowths. In particular, two generations of white mica with high-silicon content, indicative of formation at high pressure, are separated by an overgrowth with low-silicon content that formed during exhumation at low pressures. Furthermore, the trace-element signatures of distinct zones within zircon and allanite also reveal two episodes of high-pressure metamorphism, separated by a period of rapid exhumation. We use uranium–lead dating of zircon and allanite overgrowths to constrain the timing of this subduction–exhumation–subduction cycle to 79–65 Myr ago. We conclude that slices of the Sesia zone crust experienced two cycles of burial to mantle depths in less than 20 million years. The yo-yo subduction occurred during oblique convergence between the African and European plates, which involved a continental margin. Individual rock units are predicted by tectonic models to undergo numerous, complex cycles of subduction. Analysis of high-pressure rocks exposed in the Sesia zone, Italian Western Alps, suggest that slices of the crust underwent two distinct episodes of subduction to mantle depths in fewer than 20 million years.

Converging lines of evidence suggest that, during the late Archean, Earth completed its transition from a stagnant-lid to a plate tectonics regime, although how and when this transition occurred is debated. The geological record indicates that some form of subduction, a key component of plate tectonics—has operated since the Mesoarchean, even though the tectonic style and timescales of burial and exhumation cycles within ancient convergent margins are poorly constrained. Here, we present a Neoarchean pressure–temperature–time ( P–T–t ) path from supracrustal rocks of the transpressional Yilgarn orogen (Western Australia), which documents how sea-floor-altered rocks underwent deep burial then exhumation during shortening that was unrelated to the episode of burial. Archean subduction, even if generally short-lived, was capable of producing eclogites along converging lithosphere boundaries, although exhumation processes in those environments were likely less efficient than today, such that return of high-pressure rocks to the surface was rare. Supracrustal rocks of the Yilgarn orogen underwent deep burial, and later syn-shortening exhumation. Archean exhumation processes were likely less efficient that today, so that complete exhumation of high-pressure rocks was rare and accidental.