Pressure and temperature conditions for crystallization of metamorphic allanite and monazite in metapelites: a case study from the Miyar Valley (high Himalayan Crystalline of Zanskar,NW India)

The textural and chemical evolution of allanite and monazite along a well‐constrained prograde metamorphic suite in the High Himalayan Crystalline of Zanskar was investigated to determine the P–T conditions for the crystallization of these two REE accessory phases. The results of this study reveals that: (i) allanite is the stable REE accessory phase in the biotite and garnet zone and (ii) allanite disappears at the staurolite‐in isograd, simultaneously with the occurrence of the first metamorphic monazite. Both monazite and allanite occur as inclusions in staurolite, indicating that the breakdown of allanite and the formation of monazite proceeded during staurolite crystallization. Staurolite growth modelling indicates that staurolite crystallized between 580 and 610 °C, thus setting the lower temperature limit for the monazite‐forming reaction at ~600 °C. Preservation of allanite and monazite inclusions in garnet (core and rim) constrains the garnet molar composition when the first monazite was overgrown and subsequently encompassed by the garnet crystallization front. Garnet growth modelling and the intersection of isopleths reveal that the monazite closest to the garnet core was overgrown by the garnet advancing crystallization front at 590 °C, which establishes an upper temperature limit for monazite crystallization. Significantly, the substitution of allanite by monazite occurs in close spatial proximity, i.e. at similar P–T conditions, in all rock types investigated, from Al‐rich metapelites to more psammitic metasedimentary rocks. This indicates that major silicate phases, such as staurolite and garnet, do not play a significant role in the monazite‐forming reaction. Our data show that the occurrence of the first metamorphic monazite in these rocks was mainly determined by the P–T conditions, not by bulk chemical composition. In Barrovian terranes, dating prograde monazite in metapelites thus means constraining the time when these rocks reached the 600 °C isotherm.     

Variscan relicts in Alpine high-P pelitic rocks from Samos (Greece): evidence from multi-stage garnet and its included minerals

Porphyroblastic garnet schists from northern Samos contain in their matrix the assemblage Ca‐rich garnet + phengite + paragonite ± chloritoid equilibrated at ～530 °C and ～19 kbar during early Tertiary metamorphism. These high‐pressure/low‐temperature (HP‐LT) metapelitic rocks also exhibit mineralogical and microstructural evidence of an older, higher temperature metamorphism. Large, centimetre‐sized Fe‐rich garnet showing growth zoning developed discontinuous, <0.5 mm thick, Ca‐rich and Mn‐poor overgrowths, compositionally matching small (<1 mm) high‐P matrix garnet. Because the discontinuous garnet rims are in textural and chemical equilibrium with Alpine high‐P minerals, the central parts of the garnet porphyroblasts were found to have formed prior to the Tertiary metamorphism. This is supported by electron microprobe U‐Th‐Pb dating of monazite inclusions yielding partly reset Variscan ages between 360 and 160 Ma. Monazite‐xenotime and garnet‐muscovite thermometry applied to inclusions in the pre‐Alpine garnet yielded temperatures of 600–625 °C (at 3–8 kbar). Prismatic Al‐rich pseudomorphs, possibly after kyanite/sillimanite, and inclusions in garnet composed of white K‐Na mica + quartz ± albite ± K feldspar, interpreted as possible replacements of an intermediate K‐Na feldspar, further support Variscan amphibolite facies conditions. The Samos metapelites thus experienced higher temperatures during the Variscan than during Alpine metamorphism. Diffusional relaxation was very limited between pre‐Alpine garnet and Alpine garnet; both were filled with Alpine garnet along overgrowths and fractures. Fluid‐mediated intergranular element transport, enhanced by deformation, appears crucial in transforming the Variscan garnet into a grossular richer composition during Alpine subduction‐zone metamorphism. At such conditions, dissolution–reprecipitation appears to be a much more effective mechanism for modifying garnet compositions than diffusion. Amphibolite facies conditions are typical for Variscan basement relics exposed in central Cycladic and Dodecanese islands as well as in eastern Crete. The Samos metapelites studied comprise a north‐eastern extension of these basement occurrences.     

Residence and redistribution of REE, Y, Zr, Th and U during granulite-facies metamorphism: behaviour of accessory and major phases in peraluminous granulites of central Spain

Accessory minerals are thought to play a key role in controlling the behaviour of certain trace elements such as REE, Y, Zr, Th and U during crustal melting processes under high-grade metamorphic conditions. Although this is probably the case at middle crustal levels, when a comparison is made with granulite-facies lower crustal levels, differences are seen in trace element behaviour between accessory minerals and some major phases. Such a comparison can be made in Central Spain where two granulite-facies terranes have equilibrated under slightly different metamorphic conditions and where lower crustal xenoliths are also found. Differences in texture and chemical composition between accessory phases found in leucosomes and leucogranites and those of melanosomes and protholiths indicate that most of the accessory minerals in melt-rich migmatites are newly crystallized. This implies that an important redistribution of trace elements occurs during the early stages of granulite-facies metamorphism. In addition, the textural position of the accessory minerals with respect to the major phases is crucial in the redistribution of trace elements when melting proceeds via biotite dehydration melting reactions. In granulitic xenoliths from lower crustal levels, the situation seems to be different, as major minerals show high concentration of certain trace elements, the distribution of which is thus controlled by reactions involving final consumption of Al-Ti-phlogopite. A marked redistribution of HREE–Y–Zr between garnet and xenotime (where present) and zircon, but also of LREE between feldspars (K-feldspar and plagioclase) and monazite, is suggested.     

Prograde destruction and formation of monazite and allanite during contact and regional metamorphism of pelites: petrology and geochronology

The conditions at which monazite and allanite were produced and destroyed during prograde metamorphism of pelitic rocks were determined in a Buchan and a Barrovian regional terrain and in a contact aureole, all from northern New England, USA. Pelites from the chlorite zone of each area contain monazite that has an inclusion-free core surrounded by a highly irregular, inclusion-rich rim. Textures and ²⁰⁸Pb/²³²Th dates of these monazites in the Buchan terrain, obtained by ion microprobe, suggest that they are composite grains with detrital cores and very low-grade metamorphic overgrowths. At exactly the biotite isograd in the regional terrains, composite monazite disappears from most rocks and is replaced by euhedral metamorphic allanite. At precisely the andalusite or kyanite isograd in all three areas, allanite, in turn, disappears from most rocks and is replaced by subhedral, chemically unzoned monazite neoblasts. Allanite failed to develop at the biotite isograd in pelites with lower than normal Ca and/or Al contents, and composite monazite survived at higher grades in these rocks with modified texture, chemical composition, and Th-Pb age. Pelites with elevated Ca and/or Al contents retained allanite in the andalusite or kyanite zone. The best estimate of the time of peak metamorphism at the andalusite or kyanite isograd is the mean Th-Pb age of metamorphic monazite neoblasts that have not been affected by retrograde metamorphism: 364.3Dž.5 Ma in the Buchan terrain, 352.9NJ.9 Ma in the Barrovian terrain, and 403.4LJ.9 Ma in the contact aureole. Some metamorphic monazites from the Buchan terrain have ages partially to completely reset during an episode of retrograde metamorphism at 343.1Nj.1 Ma. Interpretation of Th-Pb ages of individual composite monazite grains is complicated by the occurrence of subgrain domains of detrital material intergrown with domains of material formed or recrystallized during prograde and retrograde metamorphism.     

Contrasting magmas in metapelitic and metapsammitic migmatites in the Cooma Complex, Australia

Metapelite-derived migmatites (“bedded migmatites”) formed in the low-pressure/high-temperature (LPHT) Cooma Complex, southeastern Australia, contain magma (neosome and leucosome) confined to the metapelitic beds in which they were generated. The metapsammitic beds were more ductile than the metapelitic beds (and the metapelitic parts of graded beds), which underwent fracture and boudinage, thereby providing space for the magma, though some also occurs in axial surface folia. Transitions from bedded to stromatic migmatites can be seen, but the magma mainly remained in the metapelites, even in the most strongly deformed stromatic migmatites. This, together with boudinage and transposition of the leucosome, as well as microstructural evidence of quartz recrystallization, suggest that much or most of the stromatic layering was formed by solid-state deformation. In contrast, magmas (neosomes) formed by partial melting of feldspathic metapsammites at Cooma moved out of their parent rocks, and coalesced into veins and small intrusions of diatexite, because (1) the host rocks deformed more homogeneously, and no interboudin space was made for the melts, and (2) the melt escape threshold was exceeded, probably with the assistance of deformation. Metapsammite melting occurred after solidification of the metapelite-derived magma, and the mobile metapsammite-derived magma (diatexite) disrupted and incorporated fragments of the metapelitic migmatites. The metapsammite-derived magma, together with this solid metapelitic material, locally coalesced into bodies closely resembling the Cooma Granodiorite.     

Coupling forward modelling of garnet growth with monazite geochronology: an application to the Rappold Complex (Austroalpine crystalline basement)

Results from forward modelling of garnet growth and U–Th–Pb chemical dating suggest three periods of metamorphism that affected metapelitic rocks of the Rappold Complex (Eastern European Alps). Garnet first grew during Barrovian-type metamorphism, possibly during the Carboniferous Variscan orogeny. The second period of metamorphism produced monazite and resulted in minor garnet growth in some samples. Variable garnet growth was controlled by changes to the effective bulk rock composition resulting from resorption of older garnet porphyroblasts. Monazite crystals have variable morphology, textures and composition, but all yield Permian ages (267 ± 12 to 274 ± 17 Ma). In samples in which there was Permian garnet growth, monazite forms isolated and randomly distributed grains. In other samples, monazite formed pseudomorphous clusters after allanite. This difference is attributed to higher transport rates of monazite-forming elements in samples which underwent dehydration reactions during renewed garnet growth. The third and final period of garnet growth took place during Eo-Alpine (Cretaceous) metamorphism. Garnet of this age displays a wart-like texture. This may reflect transport-limited growth, possibly as a result of repeated dehydration during polyphase metamorphism.     

Palaeoproterozoic evolution of the Challenger Au deposit, South Australia, from monazite geochronology

Monazite in granulite facies metatexite migmatites (Christie Gneiss) hosting the Challenger Au deposit, South Australia, records a series of growth and resorption stages over a c. 60 Myr period between 2470 and 2410 Ma. A combination of electron microprobe X‐ray mapping and in situ ion‐microprobe dating was used to delineate and date five compositional domains. The oldest prograde metamorphic components are preserved in granoblastic gneisses surrounding the deposit, and as small high‐Y cores in large monazite grains in Au‐bearing migmatites. In metatexite leucosomes, these cores were partially resorbed prior to the growth of large high‐Th monazite domains that crystallized during partial melting and stromatic migmatite development at c. 2443 Ma. Subsequent heating to biotite dehydration conditions (c. 850 °C at 7 kbar) caused further partial melting roughly 10–15 Myr later, giving rise to c. 2428 Ma domains surrounding partly resorbed 2443 Ma grains that were entrained in the higher‐temperature melts. This period of partial melting coincided with isoclinal folding culminating in dextral transpression and represents the most likely window for remobilization of Au‐bearing polymetallic sulphide melts into low‐strain domains. Localized reaction of residual melt with the granulite facies assemblage during cooling gave rise to narrow high‐Y rims dated at 2414 ± 7 Ma. Although monazite from unmineralized granoblastic gneisses and migmatitic ore zones display the same range of U‐Pb dates, monazite in migmatites displays a higher overall Ca + Th + U content, indicating that compositional heterogeneities between ore zones and host rocks developed prior to 2470 Ma, perhaps a consequence of the hydrothermal alteration inferred to have accompanied gold mineralization.     

Tectonically controlled fluid flow and water-assisted melting in the middle crust: An example from the Central Alps

Melting triggered by influx of a free aqueous fluid in the continental crust has commonly been inferred, but the source of water in such contexts remains a matter of debate. We focus on the Tertiary migmatites in the Southern Steep Belt of the Central Alps (Switzerland) to discuss the petrology, structures and geodynamic setting of water-assisted melting. These migmatites comprise various structural types (e.g. metatexites, diatexites, melt in shear zones), which reflect variable leucosome fractions. The melting event itself as well as the variable melt fractions are related to the amount of aqueous fluids. At a given P and T, melt-fractions in rocks of minimum melt composition correlate with the amount of infiltrated aqueous fluids. In more granodioritic systems the water distributes between melt and newly crystallizing hydrous phases such as amphibole, such that the melt fraction correlates with the contents of H₂O, Al, and Ca in the system. Phase-equilibrium modelling indicates that the stabilization of amphibole leads to slightly lower melt fractions than in a granitic system at the same P, T and bulk water content. Phase-equilibrium models further indicate that in the Alpine migmatite belt: (1) several wt.% water (fluid:rock ratio of  1:30) are necessary to produce the inferred melt fraction; (2) the activity of H₂O in the fluid is high; and (3) spatially associated metapelites are unlikely as a source for the required aqueous fluids.

We present a tectonic scenario for the southern margin of the Central Alps, to which these migmatites are confined, and we propose that water was produced from dehydration reactions in metapelites in the Southern Alps. We model fluid production rates at the time of melting and demonstrate that the resulting fluid flow pattern is mainly controlled by the differences in permeability between the fluid source region and melting region. The proposed model requires strong gradients in temperature and permeability for the two tectonic blocks. This is consistent with the scenario involving indenter tectonics at the boundary between the Central and the Southern Alps in Oligocene times.     

P–T–t evolution of granulite facies metamorphism and partial melting in the Winding Stair Gap,Central Blue Ridge,North Carolina,USA

The Winding Stair Gap in the Central Blue Ridge province exposes granulite facies schists, gneisses, granofelses and migmatites characterized by the mineral assemblages: garnet–biotite–sillimanite–plagioclase–quartz, garnet–hornblende–biotite–plagioclase–quartz ± orthopyroxene ± clinopyroxene and orthopyroxene–biotite–quartz. Multiple textural populations of biotite, kyanite and sillimanite in pelitic schists support a polymetamorphic history characterized by an early clockwise P–T path in which dehydration melting of muscovite took place in the stability field of kyanite. Continued heating led to dehydration melting of biotite until peak conditions of 850 ± 30 °C, 9 ± 1 kbar were reached. After equilibrating at peak temperatures, the rocks underwent a stage of near isobaric cooling during which hydrous melt ± K‐feldspar were replaced by muscovite, and garnet by sillimanite + biotite + plagioclase. Most monazite crystals from a pelitic schist display patchy zoning for Th, Y and U, with some matrix crystals having as many as five compositional zones. A few monazite inclusions in garnet, as well as Y‐rich cores of some monazite matrix crystals, yield the oldest dates of c. 500 Ma, whereas a few homogeneous matrix monazites that grew in the main foliation plane yield dates of 370–330 Ma. Culling and analysis of individual spot dates for eight monazite grains yields three age populations of 509 ± 14 Ma, 438 ± 5 Ma and 360 ± 5 Ma. These data suggest that peak‐temperature metamorphism and partial melting in the central Blue Ridge occurred during the Salinic or Taconic orogeny. Following near isobaric cooling, a second weaker thermal pulse possibly related to intrusion of nearby igneous bodies resulted in growth of monazite c. 360 Ma, coinciding with the Neoacadian orogeny.     

Fluid‐induced breakdown of monazite in medium‐grade metasedimentary rocks of the Pontremoli basement (Northern Apennines,Italy)

The last (decompression) stages of the metamorphic evolution can modify monazite microstructure and composition, making it difficult to link monazite dates with pressure and temperature conditions. Monazite and its breakdown products under fluid‐present conditions were studied in micaschist recovered from the cuttings of the Pontremoli1 well, Tuscany. Coronitic microstructures around monazite consist of concentric zones of apatite + Th‐silicate, allanite and epidote. The chemistry and microstructure of the monazite grains, which preserve a wide range of chemical dates ranging from Upper Carboniferous to Tertiary times, suggest that this mineral underwent a fluid‐mediated coupled dissolution–reprecipitation and crystallization processes. Consideration of the chemical zoning (major and selected trace elements) in garnet, its inclusion mineralogy (including xenotime), monazite breakdown products and phase diagram modelling allow the reaction history among accessory minerals to be linked with the reconstructed P–T evolution. The partial dissolution and replacement by rare earth element‐accessory minerals (apatite–allanite–epidote) occurred during a fluid‐present decompression at 510 ± 35 °C. These conditions represent the last stage of a metamorphic history consisting of a thermal metamorphic peak at 575 °C and 7 kbar, followed by the peak pressure stage occurring at 520 °C and 8 kbar. An anticlockwise P–T path or two clockwise P–T loops can fit the above P–T constraints. The former path may be related to a context of late Variscan strike‐slip‐dominated exhumation with minor Tertiary (Alpine‐related) reworking and fluid infiltration, while the latter requires an Oligocene–Miocene fluid‐present tectono‐metamorphic overprint on the Variscan paragenesis.     

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.     

Residence of REE, Y, Th and U in Granites and Crustal Protoliths; Implications for the Chemistry of Crustal Melts

A systematic study with laser ablation—ICP-MS, scanningelectron microscopy and electron microprobe revealed that 70–95wt% of REE (except Eu), Y, Th and U in granite rocks and crustalprotoliths reside within REEYThU-rich accessories whose nature,composition and associations change with the rock aluminosity.The accessory assemblage of peraluminous granites, migmatitesand high-grade rocks is composed of monazite, xenotime (in low-Cavarieties), apatite, zircon, Thorthosilicate, uraninite andbetafite-pyrochlore. Metaluminous granites have allanite, sphene,apatite, zircon, monazite and Thorthosilicaie. Peralkaline graniteshave aeschinite, fergusonite, samarskite, bastnaesite, fluocerite,allanite, sphene, zircon, monazite, xenotime and Th-orthosilicate.Granulite-grade garnets are enriched in Nd and Sm by no lessthan one order of magnitude with respect to amphibolite-gradegarnets. Granulitegrade feldspars are also enriched in LREEwith respect to amphibolite-grade feldspars. Accessories causenon-Henrian behaviour of REE, Y, Th and U during melt—solidpartitioning. Because elevated fractions of monazite, xenotimeand zircon in common migmatites are included within major minerals,their behaviour during anatexis is controlled by that of theirhost. Settling curves calculated for a convecting magma showthat accessories are too small to settle appreciably, beingseparated from the melt as inclusions within larger minerals.Biotite has the greatest tendency to include accessories, therebyindirectly controlling the geochemistry of REE, Y, Th and U.We conclude that REE, Y, Th and U are unsuitable for petrogeneticalmodelling of granitoids through equilibrium-based trace-elementfractionation equations. KEY WORDS: accessory minerals; geochemical modelling; granitoids; REE, Y, Th, U     

Why allanite may swindle about its true age

Allanite from the Tertiary Rieserferner pluton (Austrian Alps) is texturally and chemically heterogeneous. Continuous covariation trends reflect coupled substitution of Ca+Al vs. Fe+REE+Th in allanite, whereas systematic variations in La/Nd demonstrate the increasingly stronger depletion of LREE in the melt during its crystallization. Allanite samples (corrected for ²⁰⁶Pb_excess) from two rocks scatter in the concordia diagram and define discordias from 31.8±0.4 Ma and 32.2±0.4 Ma to ca. 540 Ma. The apparent inheritance does not originate from the inclusion of older allanite or a high- phase, such as monazite, xenotime, or zircon, but from the incorporation of radiogenic Pb originating from a precursor. Since allanite requires a high enrichment of Th, (U), and LREE, it may form at the expense of a Th-LREE-rich precursor in metamorphic rocks or where such a phase had dissolved in melts. Likely precursors acquire with time radiogenic Pb isotopic compositions. This Pb, if incorporated in the product mineral, may give the illusion of inheritance. The allanite samples from the Rieserferner pluton show a tendency from high Th/U_calc (30–50) in samples with an Alpine age to low Th/U_calc (4–12) in samples with distinct inheritance. This relation between extent of inheritance and apparent Th/U_calc indicates a lower Th/U_calc for a possible precursor, falling into the Th/U range commonly encountered for monazite. Precursor monazite would have originated from assimilated Palaeozoic rocks and give rise to localized enrichments of Th and LREE in the melt, thus eventually enabling the growth of allanite.Electronic Supplementary Material Supplementary material is available in the online version of this article at .Editorial responsibility: J. Hoefs     

REE distribution in some layered migmatites: constraints on their petrogenesis

The REE distributions in mesosomes, neosomes, leucosomes and melanosomes of four layered migmatites have been investigated. In one example (Arvika migmatites) the REE patterns in adjacent paragneisses, the presumed parent rock of the migmatites, were also determined. REE patterns of neosomes and mesosomes of Arvika migmatites are similar to the finegrained layers and coarse-grained layers, respectively, observed in the adjacent paragneiss. This is in agreement with the layer-by-layer paragneiss-migmatite transformation model.

The REE patterns of mesosomes and neosomes indicate that these lithologies may have been closed systems (for REE) during the formation of the migmatites. No indication of metasomatic reactions, melt segregation or injection could be detected. Within the neosomes, leucosomes are depleted and melanosomes enriched in REE contents. This is interpreted to be due to separation and concentration of accessory minerals (monazite, epidote, allanite, zircon, sphene, apatite, garnet) into the melanosomes. The behaviour of accessory minerals during migmatite formation is closely allied to that of biotite, which is also concentrated in the melanosomes.     

Petrology and U/Pb geochronology of the Telohat migmatites,Aleksod, Central Hoggar,Algeria

The Aleksod region is composed of metasedimentary rocks and large areas of biotite and hornblende-bearing migmatites. Anatexis associated with the main deformation stages, occurred under high pressure and temperature conditions estimated at 13±2 Kbar and 750±50° C. The bulk mineralogical composition of the Telohat migmatites shows that their protolith was granodioritic. Internal structures of zircons and U-Pb data suggest a polyphased evolution, with a 2131±12 Ma age for the protolith and a 609±17 Ma age for the Pan-African tectono-metamorphic evolution, thus precluding any Kibaran event in the Aleksod area. Leucosomes are richer in Sr and display lower Rb, Zr, Nb, Y, Th, U and REE contents than melanosomes wherein accessory phases are stored. Eu contents are also lower in the leucosomes but in lesser proportion than the other rare earth's, leading to a significant positive anomaly. Petrogenetic modelling accounting for accessory mineral phases clearly shows that the trace element contents of leucosomes and melanosomes follow a distribution law consistent neither with equilibrium nor fractional melting. Their trace element patterns are best explained by the model of disequilibrium melting, with mixing of a few residual phases. The present results and previous Sr isotopic data as well raise the question of disequilibrium melting in anatexis of crustal material CRPG Contribution no 782     

Polymetamorphic evolution of pelitic schists and evidence for Permian low-pressure metamorphism in the Vepor Unit, West Carpathians

Phase equilibrium modelling and monazite microprobe dating were used to characterize the polymetamorphic evolution of metapelites from the northern part of the Vepor Unit, West Carpathians. Three generations of garnet and associated metamorphic assemblages found in these rocks correspond to three distinct metamorphic events related to the Variscan orogeny, a Permian phase of crustal extension and the Alpine orogeny. Variscan staurolite‐bearing and Alpine chloritoid‐bearing assemblages record medium‐temperature and medium‐pressure regional metamorphisms reaching 540–570 °C/5–7.5 kbar and 530–550 °C/5–6.5 kbar respectively. The Permian metamorphic assemblage involves garnet, andalusite, sillimanite, biotite, muscovite, plagioclase and corundum and locally forms silica‐undersaturated andalusite‐biotite‐spinel coronas around older staurolite. The transition from andalusite to sillimanite indicates a prograde low‐pressure and medium‐temperature metamorphism characterized by temperature increase from 500 to 650 °C at ～3 kbar. As accessory monazite is abundant in the rocks, an attempt was made to derive its age of formation by means of electron microprobe‐based Th‐U‐Pb chemical dating. Despite the polymetamorphic nature of the metapelites, the monazite yielded uniform Permian ages. Microstructures confirm that monazite was formed in relation to the low‐pressure and medium‐temperature paragenesis, and the weighted average ages obtained for two different samples are 278 ± 5 and 275 ± 12 Ma respectively. The virtual lack of Variscan and Alpine monazite populations points to interesting aspects concerning the growth systematics of monazite in metamorphic rocks.     

Accessory phase petrogenesis in relation to major phase assemblages in pelites from the Nelson contact aureole, southern British Columbia

Monazite petrogenesis in the Nelson contact aureole is the result of allanite breakdown close to, but downgrade and therefore independent of, major phase isograds involving cordierite, andalusite and staurolite. The development of garnet downgrade of the staurolite and andalusite isograds does not appear to affect the onset of the allanite-to-monazite reaction but does affect the textural development of monazite. In lower pressure, garnet-absent rocks, allanite breakdown results in localized monazite growth as pseudomorphous clusters. In higher pressure, garnet-bearing rocks, allanite breakdown produces randomly distributed, lone grains of monazite with no textural relationship to the original reaction site. Fluids liberated from hydrous phases (chlorite, muscovite) during garnet formation may have acted as a flux to distribute light rare earth elements more widely within the rock upon allanite breakdown, preventing the localized formation of monazite pseudomorphs. Despite these textural differences, both types of monazite have very similar chemistry and an indistinguishable age by electron microprobe chemical dating (157 ± 6.4 Ma). This age range is within error of isotopic ages determined by others for the Nelson Batholith. Garnet from the garnet, staurolite and andalusite zones shows euhedral Y zoning typified by a high-Y core, low-Y collar and moderate-Y annulus, the latter ascribed to allanite breakdown during garnet growth in the garnet zone. The cause of the transition from high-Y core to low-Y collar, traditionally interpreted to be due to xenotime consumption, is unclear because of the ubiquitous presence of xenotime. Accessory phase geothermometry involving monazite, xenotime and garnet returns inconsistent results, suggesting calibration problems or a lack of equilibration between phases.     

Relating zircon and monazite domains to garnet growth zones: age and duration of granulite facies metamorphism in the Val Malenco lower crust

Zircon from a lower crustal metapelitic granulite (Val Malenco, N‐Italy) display inherited cores, and three metamorphic overgrowths with ages of 281 ± 2, 269 ± 3 and 258 ± 4 Ma. Using mineral inclusions in zircon and garnet and their rare earth element characteristics it is possible to relate the ages to distinct stages of granulite facies metamorphism. The first zircon overgrowth formed during prograde fluid‐absent partial melting of muscovite and biotite apparently caused by the intrusion of a Permian gabbro complex. The second metamorphic zircon grew after formation of peak garnet, during cooling from 850 °C to c. 700 °C. It crystallized from partial melts that were depleted in heavy rare earth elements because of previous, extensive garnet crystallization. A second stage of partial melting is documented in new growth of garnet and produced the third metamorphic zircon. The ages obtained indicate that the granulite facies metamorphism lasted for about 20 Myr and was related to two phases of partial melting producing strongly restitic metapelites. Monazite records three metamorphic stages at 279 ± 5, 270 ± 5 and 257 ± 4 Ma, indicating that formation ages can be obtained in monazite that underwent even granulite facies conditions. However, monazite displays less clear relationships between growth zones and mineral inclusions than zircon, hampering the correlation of age to metamorphism. To overcome this problem garnet–monazite trace element partitioning was determined for the first time, which can be used in future studies to relate monazite formation to garnet growth.     

Protracted fluid-induced melting during Barrovian metamorphism in the Central Alps

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.     

Using monazite and zircon petrochronology to constrain the P–T–t evolution of the middle crust in the Bhutan Himalaya

The growth and dissolution behaviour of accessory phases (and especially those of geochronological interest) in metamorphosed pelites depends on, among others, the bulk composition, the prograde metamorphic evolution and the cooling path. Monazite and zircon are arguably the most commonly used geochronometers for dating felsic metamorphic rocks, yet crystal growth mechanisms as a function of rock composition, pressure and temperature are still incompletely understood. Ages of different growth zones in zircon and monazite in a garnet‐bearing anatectic metapelite from the Greater Himalayan Sequence in NW Bhutan were investigated via a combination of thermodynamic modelling, microtextural data and interpretation of trace‐element chemical ‘fingerprint’ indicators in order to link them to the metamorphic stage at which they crystallized. Differences in the trace‐element composition (HREE, Y, Eu_N/Eu*_N) of different phases were used to track the growth/dissolution of major (e.g. plagioclase, garnet) and accessory phases (e.g. monazite, zircon, xenotime, allanite). Taken together, these data constrain multiple pressure–temperature–time (P–T–t) points from low temperature (<550 °C) to upper amphibolite facies (partial melting, >700 °C) conditions. The results suggest that the metapelite experienced a cryptic early metamorphic stage at c. 38 Ma at <550 °C, ≥0.85 GPa during which plagioclase was probably absent. This was followed by a prolonged high‐T, medium‐pressure (~600 °C, 0.55 GPa) evolution at 35–29 Ma during which the garnet grew, and subsequent partial melting at >690 °C and >18 Ma. Our data confirm that both geochronometers can crystallize independently at different times along the same P–T path and that neither monazite nor zircon necessarily provides timing constraints on ‘peak’ metamorphism. Therefore, collecting monazite and zircon ages as well as major and trace‐element data from major and accessory phases in the same sample is essential for reconstructing the most coherent metamorphic P–T–t evolution and thus for robustly constraining the rates and timescales of metamorphic cycles.