Constraints from monazite and xenotime growth modelling in the MnCKFMASH‐PYCe system on the P–T path of a metapelite from Shillong‐Meghalaya Plateau: implications for the Indian shield assembly

The Palaeo‐Mesoproterozoic metapelite granulites from northern Garo Hills, western Shillong‐Meghalaya Gneissic Complex (SMGC), northeast India, consist of resorbed garnet, cordierite and K‐feldspar porphyroblasts in a matrix comprising shape‐preferred aggregates of biotite±sillimanite+quartz that define the penetrative gneissic fabric. An earlier assemblage including biotite and sillimanite occurs as inclusions within the garnet and cordierite porphyroblasts. Staurolite within cordierite in samples without matrix sillimanite is interpreted to have formed by a reaction between the sillimanite inclusion and the host cordierite during retrogression. Accessory monazite occurs as inclusions within garnet as well as in the matrix, whereas accessory xenotime occurs only in the matrix. The monazite inclusions in garnet contain higher Ca, and lower Y and Th/U than the matrix monazite outside resorbed garnet rims. On the other hand, matrix monazite away from garnet contains low Ca and Y, and shows very high Th/U ratios. The low Th/U ratios (<10) of the Y‐poor garnet‐hosted monazite indicate subsolidus formation during an early stage of prograde metamorphism. A calculated P–T pseudosection in the MnCKFMASH‐PYCe system indicates that the garnet‐hosted monazite formed at <3 kbar/600 °C (Stage A). These P–T estimates extend backward the previously inferred prograde P–T path from peak anatectic conditions of 7–8 kbar/850 °C based on major mineral equilibria. Furthermore, the calculated P–T pseudosections indicate that cordierite–staurolite equilibrated at ~5.5 kbar/630 °C during retrograde metamorphism. Thus, the P–T path was counterclockwise. The Y‐rich matrix monazite outside garnet rims formed between ~3.2 kbar/650 °C and ~5 kbar/775 °C (Stage B) during prograde metamorphism. If the effect of bulk composition change due to open system behaviour during anatexis is considered, the P–T conditions may be lower for Stage A (<2 kbar/525 °C) and Stage B (~3 kbar/600 °C to ~3.5 kbar/660 °C). Prograde garnet growth occurred over the entire temperature range (550–850 °C), and Stage‐B monazite was perhaps initially entrapped in garnet. During post‐peak cooling, the Stage‐B monazite grains were released in the matrix by garnet dissolution. Furthermore, new matrix monazite (low Y and very high Th/U ≤80, ~8 kbar/850–800 °C, Stage C), some monazite outside garnet rims (high Y and intermediate Th/U ≤30, ~8 kbar/800–785 °C, Stage D), and matrix xenotime (<785 °C) formed through post‐peak crystallization of melt. Regardless of textural setting, all monazite populations show identical chemical ages (1630–1578 Ma, ±43 Ma). The lithological association (metapelite and mafic granulites), and metamorphic age and P–T path of the northern Garo Hills metapelites and those from the southern domain of the Central Indian Tectonic Zone (CITZ) are similar. The SMGC was initially aligned with the southern parts of CITZ and Chotanagpur Gneissic Complex of central/eastern India in an ENE direction, but was displaced ~350 km northward by sinistral movement along the north‐trending Eastern Indian Tectonic Zone in Neoproterozoic. The southern CITZ metapelites supposedly originated in a back‐arc associated with subducting oceanic lithosphere below the Southern Indian Block at c. 1.6 Ga during the initial stage of Indian shield assembly. It is inferred that the SMGC metapelites may also have originated contemporaneously with the southern CITZ metapelites in a similar back‐arc setting.     

Monazite–xenotime miscibility gap thermometry. I. An empirical calibration

Rare earth element (REE) and yttrium concentrations of coexisting monazite and xenotime were determined from a suite of seven metapelites from the Variscan fold belt in NE Bavaria, Germany. The metapelites include a continuous prograde, mainly low-P (3–5 kbar) metamorphic profile from greenschist (c. 400 °C) to lower granulite facies conditions (c. 700 °C). The LREE (La–Sm) are incorporated preferentially in monoclinic monazite (REO₉ polyhedron), whereas the HREE plus Y are concentrated in tetragonal xenotime (REO₈ polyhedron). The major element concentrations of both phases in all rocks are very similar and do not depend on metamorphic grade. Monazite consists mainly of La, Ce and Nd (La_0.20–0.23, Ce_0.41–0.45, Nd_0.15–0.18)PO₄, all other elements are below 6 mol%. Likewise, xenotime consists mainly of YPO₄ with some Dy and Gd solid solutions (Y_0.76–0.80, Dy_0.05–0.07, Gd_0.04–0.06). In contrast, the minor HREE concentrations in monazite increase strongly with increasing metamorphic grade: Y, Dy and Gd increase by a factor of 3–5 from greenschist to granulite facies rocks. Monazite crystals often show zonation with cores low in HREE and rims high in HREE that is interpreted as growth zonation attained during prograde metamorphism. Similarly, Sm and Nd in xenotimes increase by a factor of 3–4 with increasing metamorphic grade. Prograde zonation in single crystals of xenotime was not observed. The X_HREE+Y in monazite and X_LREE in xenotime of the seven rocks define two limbs along the strongly asymmetric miscibility gap from c. 400 °C to 700 °C. The empirical calibration of the monazite miscibility gap limb coexisting with xenotime is appropriate for geothermometry. Due to its contents of U and Th, monazite has often been used for U–Pb age determination. The combination of our empirical thermometer on prograde zoned monazite along with possible age determination of zoned single crystals may provide information about prograde branches of temperature–time paths.     

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.     

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.     

Trace-element distributions in silicates during prograde metamorphic reactions: implications for monazite formation

To assess the petrogenetic relationship between monazite and major silicates during prograde metamorphism, REE were measured across coexisting zoned silicates in garnet through kyanite‐grade pelitic schists from the Great Smoky Mountains, western Blue Ridge terrane, southern Appalachians, to establish REE concentrations and distributions before and after the monazite‐in isograd, and to identify the role major silicates play in the formation of monazite. Results indicate significant scavenging of light rare‐earth elements (LREE) from silicates during the monazite‐in isograd reaction; however, the absolute concentration of LREE hosted in the silicates was insufficient to produce monazite in the quantity observed in these schists. Monazite must have formed mainly from either the dissolution of allanite or some other source of concentrated LREE (possibly adsorbed onto grain boundaries), even though direct evidence for allanite is lacking in a majority of the samples. Laser‐ablation ICP‐MS analyses and theoretical thermodynamic calculations show that monazite may have formed as a result of contributions from both allanite and major silicates. Allanite breakdown initially formed monazite, and monazite production drew LREE liberated from allanite, major silicates and possibly from crystal boundaries. In many rocks the reaction was further promoted by the staurolite‐in reaction, allowing for rapid, isogradic monazite growth.     

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.     

Zonal REE + Y profiles in garnet and their genetic implications: A case study of metapelites from the northern Ladoga region

The objective of this study is to provide insights into the REE and Y behavior during garnet porphyroblast formation in staurolite-bearing schists as a constituent of Late Paleoproterozoic metapelites of the Ladoga Complex. The MnNCKFMASH P–T pseudosection for a single sample and Grt–Bt thermometry indicate that the garnet core grew at 520°C and under 7.0–7.2 kbar in the Grt–Bt–Pl–Chl–Ms–Zo field, whereas the garnet rim was equilibrated at 590–600°C and under 3.5–4.0 kbar. The measured zoning profiles are strongly depleted in REE + Y in the garnet core containing high Mn and Ca concentrations. The intermediate zone of garnet is enriched in La, Ce, Pr, and Nd (inner LREE + Nd annulus), as well as in Dy, Er, Yb, Lu, and Y (outer HREE + Y + Dy annulus). According to pseudosection analysis, these peaks were probably produced owing to breakdown of epidote-group minerals (allanite, REE-rich epidote) at T < 535°C and P > 6.5 kbar. Towards the rim, the HREE + Y contents gradually decrease, whereas MREE (Sm, Eu, Gd) display an inverse trend. The rim also exhibits a negative Eu anomaly. The former tendency reflects an increase in temperature during garnet crystallization and partitioning of elements between garnet and monazite. It is thought that the latter is linked to oppositely directed change in garnet-monazite partition coefficients for HREE and MREE with increasing temperature.     

Two-stage metamorphic evolution of the Bemarivo Belt of northern Madagascar: constraints from reaction textures and in situ monazite dating

New results on the pressure–temperature–time evolution, deduced from conventional geothermobarometry and in situ U‐Th‐total Pb dating of monazite, are presented for the Bemarivo Belt in northern Madagascar. The belt is subdivided into a northern part consisting of low‐grade metamorphic epicontinental series and a southern part made up of granulite facies metapelites. The prograde metamorphic stage of the latter unit is preserved by kyanite inclusions in garnet, which is in agreement with results of the garnet (core)‐alumosilicate‐quartz‐plagioclase (inclusions in garnet; GASP) equilibrium. The peak metamorphic stage is characterized by ultrahigh temperatures of ～900–950 °C and pressures of ～9 kbar, deduced from GASP equilibria and feldspar thermometry. In proximity to charnockite bodies, garnet‐sillimanite‐bearing metapelites contain aluminous orthopyroxene (max. 8.0 wt% Al₂O₃) pointing to even higher temperatures of ～970 °C. Peak metamorphism is followed by near‐isothermal decompression to pressures of 5–7 kbar and subsequent near‐isobaric cooling, which is demonstrated by the extensive late‐stage formation of cordierite around garnet. Internal textures and differences in chemistry of metapelitic monazite point to a polyphasic growth history. Monazite with magmatically zoned cores is rarely preserved, and gives an age of c. 737 ± 19 Ma, interpreted as the maximum age of sedimentation. Two metamorphic stages are dated: M1 monazite cores range from 563 ± 28 Ma to 532 ± 23 Ma, representing the collisional event, and M2 monazite rims (521 ± 25 Ma to 513 ± 14 Ma), interpreted as grown during peak metamorphic temperatures. These are among the youngest ages reported for high‐grade metamorphism in Madagascar, and are supposed to reflect the Pan‐African attachment of the Bemarivo Belt to the Gondwana supercontinent during its final amalgamation stage. In the course of this, the southern Bemarivo Belt was buried to a depth of >25 km. Approximately 25–30 Myr later, the rocks underwent heating, interpreted to be due to magmatic underplating, and uplift. Presumably, the northern part of the belt was also affected by this tectonism, but buried to a lower depth, and therefore metamorphosed to lower grades.     

Phase equilibria of bastnaesite,allanite, and monazite: Bastnaesite-out isograde in metapelites of the Vorontsovskaya group,Voronezh crystalline massif

Paleoproterozoic metapelites of the Vorontsovskaya structure contain accessory REE phosphates (monazite, xenotime, and REE-apatite), fluorine-carbonates (bastnaesite and synchysite), and silicate (allanite). Analysis of phase equilibria involving REE-bearing minerals indicates that bastnaesite is stable only in the greenschist facies and decomposes with the synthesis of monazite at temperatures below the staurolite isograde (490–500°C) at a pressure of 3 kbar. Monazite first appears in the greenschist facies, and its stability expands with increasing temperature, including the granulite facies. A diversity of reaction textures suggests that the mineral is formed in the garnet zone by a reaction of bastnaesite with apatite and by the partial decomposition of REE-bearing chlorite. Monazite is produced in the garnet and staurolite zones by a reaction of allanite with apatite and by a decomposition reaction of REE-bearing apatite.     

Phase relations of REE-bearing minerals during the metamorphism of carbonaceous shales in the Tim-Yastrebovskaya structure,Voronezh Crystalline Massif,Russia

Paleoproterozoic carbonaceous shales in the Tim-Yastrebovskii ancient rift, which underwent zonal metamorphism at 350–550°C, contain REE mineralization of silicates (allanite, thorite, and Ce-P huttonite) fluorcarbonates (bastnaesite and synchysite), phosphates (monazite and xenotime), and REE-bearing apatite. The reason for the wide occurrence of bastnaesite and other REE minerals is relatively high REE concentrations in the sulfide-bearing carbonaceous shales, with these elements accumulated in the organic matter in the course of diagenesis. Reaction textures with REE-bearing chlorite, bastnaesite, and allanite suggest that REE-bearing chlorite and bastnaesite provided REE for the forming of higher temperature allanite and monazite. This is corroborated by the REE patterns of the monazite, allanite, and bastnaesite, which are almost identical and are characterized by the strong predominance of LREE. The replacements of REE minerals during metamorphism at 350–550°C took place via a number successive transitions: (1) Mnz → Aln, Chl _REE → Bst, Chl _REE → Aln, Bst → Aln and (2) Bst → Mnz and Ap _LREE → Mnz. These replacements can be accounted for by prograde metamorphic reactions.     

Re-evaluating monazite as a record of metamorphic reactions

This study presents a re-examination of historical specimens (DG136 and DG167) from the Monashee complex in the southeastern Canadian Cordillera that are critical to the current understanding of rare earth element (REE) distribution between garnet and monazite (and other accessory minerals) during metamorphism. Nine-hundred and fifty-one new monazite petrochronology spot analyses on 29 different grains across two specimens outline detailed (re)crystallization histories. Trace element data collected from the same ablated volume, interpreted in the context of new phase equilibria modelling that includes monazite, xenotime and apatite, link ages to specific portions of the pressure–temperature (P-T) paths followed by the specimens. These linkages are further informed by garnet Lu-Hf geochronology and xenotime petrochronology. The clockwise P-T paths indicate prograde metamorphism was ongoing by ca. 80 Ma in both specimens. The structurally deeper specimen, DG136, records peak P-T conditions of ~755–770 ℃ and 8.8–10.4 kbar, interpreted to coincide with (re-)crystallization of low Y monazite at ～75–70 Ma. Near-rim garnet isopleths from DG167 cross in the observed peak assemblage field at ～680 °C and 9.3 kbar. These conditions are interpreted to correspond with low Y monazite (re-)crystallisation at ～65 Ma. Both specimens record decompression along their retrograde path coincident with high Y 70–55 Ma and 65–55 Ma monazite populations in DG136 and DG167, respectively. These findings broadly agree with those initially reported ～20 years ago and confirm early interpretations using trace elements in monazite as generally reliable markers of metamorphic reactions. Modern phase equilibria modelling and in situ petrochronological analysis, however, provide additional insight into monazite behaviour during anatexis and the effects of potential trace element buffering by REE-bearing phases such as apatite.     

Ultrahigh‐temperature osumilite gneisses in southern Madagascar record combined heat advection and high rates of radiogenic heat production in a long‐lived high‐T orogen

We report the discovery of osumilite in ultrahigh‐temperature (UHT) metapelites of the Anosyen domain, southern Madagascar. The gneisses equilibrated at ~930°C/0.6 GPa. Monazite and zircon U–Pb dates record 80 Ma of metamorphism. Monazite compositional trends reflect the transition from prograde to retrograde metamorphism at 550 Ma. Eu anomalies in monazite reflect changes in fO₂ relative to quartz–fayalite–magnetite related to the growth and breakdown of spinel. The ratio Gd/Yb in monazite records the growth and breakdown of garnet. High rates of radiogenic heat production were the primary control on metamorphic grade at the regional scale. The short duration of prograde metamorphism in the osumilite gneisses (<29 ± 8 Ma) suggests that a thin mantle lithosphere (<80 km) or advective heating may have also been important in the formation of this high‐T, low‐P terrane.     

Behavior of accessory phases and redistribution of Zr,REE, Y,Th, and U during metamorphism and partial melting of metapelites in the lower crust: an example from the Kinzigite Formation of Ivrea-Verbano,NW Italy

This study is aimed at understanding the behavior of monazite, xenotime, apatite and zircon, and the redistribution of Zr, REE, Y, Th, and U among melt, rock-forming and accessory phases in a prograde metamorphic sequence, the Kinzigite Formation of Ivrea-Verbano, NW Italy, that may represent a section from the middle to lower continental crust. Metamorphism ranges from middle amphibolite to granulite facies and metapelites show evidence of intense partial melting and melt extraction. The appearance of melt controls the grain size, fraction of inclusions and redistribution of REE, Y, Th, and U among accessories and major minerals. The textural evolution of zircon and monazite follows, in general, the model of Watson et al. (1989). Apatite is extracted from the system dissolved into partial melts. Xenotime is consumed in garnet-forming reactions and is the first source for the elevated Y and HREE contents of garnet. Once xenotime is exhausted, monazite, apatite, zircon, K-feldspar, and plagioclase are progressively depleted in Y, HREE, and MREE as the modal abundance of garnet increases. Monazite is severely affected by two retrograde reactions, which may have consequences for U-Pb dating of this mineral. Granulite-grade metapelites (stronalites) are significantly richer in Ti, Al, Fe, Mg, Sc, V, Cr, Zn, Y, and HREE, and poorer in Li, Na, K, Rb, Cs, Tl, U, and P, but have roughly the same average concentration of Cu, Sr, Pb, Zr, Ba, LREE, and Th as amphibolite-grade metapelites (kinzigites). The kinzigite-stronalite transition is marked by the sudden change of Th/U from 5–6 to 14–15, the progressive increase of Nb/Ta, and the decoupling of Ho from Y. Leucosomes were saturated in zircon, apatite, and (except at the lowest degree of partial melting) monazite. Their REE patterns, especially the magnitude of the Eu anomaly, depend on the relative proportion of feldspars and monazite incorporated into the melt. The presence of monazite in the source causes an excellent correlation of LREE and Th, with nearly constant Nd/Th ≈ 2.5–3. The U depletion and increase in Th/U characteristic of granulite facies only happens in monazite-bearing rocks. It is attributed to enhancement of the U partitioning in the melt due to elevated Cl activity followed by the release of a Cl-rich F-poor aqueous fluid at the end of the crystallization of leucosomes. Halide activity in partial melts was buffered by monazite and apatite. Since the U (and K) depletion does not substantially affect the heat-production of metapelites, and mafic granulites maintain similar Th/U and abundance of U and Th as their unmetamorphosed equivalents, it seems that geochemical changes associated to granulitization have only a minor influence on heat-production in the lower crust.     

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.     

Polymetamorphism in garnet micaschists of the Saualpe Eclogite Unit (Eastern Alps,Austria), resolved by automated SEM methods and EMP–Th–U–Pb monazite dating

Polymetamorphic garnet micaschists from the Austroalpine Saualpe Eclogite Unit (Kärnten, Austria, Eastern Alps) display complex microstructural and mineral–chemical relationships. Automated scanning electron microscopy routines with energy dispersive X‐ray (EDX) spectral mapping were applied for monazite detection and garnet mineral–chemical characterization. When the Fe, Mg, Mn and Ca element wt% compositions are used as generic labels for garnet EDX spectra, complex zonations and porphyroblast generations can be resolved in complete thin sections for selective electron‐microprobe analyses. Two garnet porphyroblast generations and diverse monazite age populations have been revealed in low‐Ca and high‐Al‐metapelites. Garnet 1 has decreasing Mn, constant Ca and significantly increasing Mg from cores to rims. Geothermobarometry of garnet 1 assemblages signals a crystallization along a M1 prograde metamorphism at ~650 °C/6–8 kbar. Sporadic monazite 1 crystallization started at c. 320 Ma. Subsequent pervasive 300–250 Ma high‐Y and high‐Gd monazite 1 formation during decompression coincided with the intrusion of Permian and Early Triassic pegmatites. Monazite 1 crystallized along the margin of garnet 1. Coronas of apatite and allanite around the large 320–250 Ma monazite signal a retrogressive stage. These microstructures suggest a Carboniferous‐to‐Early‐Permian age for the prograde M1 event with garnet 1. Such a M1 event at an intermediate‐P/T gradient has not yet been described from the Saualpe, and preceded a Permo‐Triassic low‐P stage. The M2 event with garnet 2 postdates the corona formation around Permian monazite. Garnet 2 displays first increasing X_Ca at decreasing X_Mg, then increasing X_Ca and X_Mg, and finally decreasing X_Ca with increasing X_Mg, always at high Ca and Mg, and low Mn. This records a P–T evolution which passed through eclogite facies conditions and reached maximum temperatures at ~750 °C/14 kbar during decompression‐heating. A monazite 2 population (94–86 Ma) with lower Y and Gd contents crystallized at decreasing pressure during the Cretaceous (Eo‐Alpine) metamorphism M2 at a high‐P/T gradient. The Saualpe Eclogite Unit underwent two distinct clockwise metamorphic cycles at different P–T conditions, related to continental collisions under different thermal regimes. This led to a characteristic distribution pattern of monazite ages in this unit which is different from other Austroalpine basement areas.     

Coupled garnet Lu–Hf and monazite U–Pb geochronology constrain early convergent margin dynamics in the Ross orogen,Antarctica

The Ross orogen of Antarctica is an extensive (>3000 km‐long) belt of deformed and metamorphosed sedimentary rocks and granitoid batholiths, which formed during convergence and subduction of palaeo‐Pacific lithosphere beneath East Gondwana in the Neoproterozoic–early Palaeozoic. Despite its prominent role in Gondwanan convergent tectonics, and a well‐established magmatic record, relatively little is known about the metamorphic rocks in the Ross orogen. A combination of garnet Lu–Hf and monazite U–Pb (measured by laser‐ablation split‐stream ICP‐MS) geochronology reveals a protracted metamorphic history of metapelites and garnet amphibolites from a major segment of the orogen. Additionally, direct dating of a common rock‐forming mineral (garnet) and accessory mineral (monazite) allows us to test assumptions that are commonly used when linking accessory mineral geochronology to rock‐forming mineral reactions. Petrography, mineral zoning, thermobarometry and pseudosection modelling reveal a Barrovian‐style prograde path, reaching temperatures of ~610–680 °C. Despite near‐complete diffusional resetting of garnet major element zoning, the garnet retains strong rare earth element zoning and preserves Lu–Hf dates that range from c. 616–572 Ma. Conversely, monazite in the rocks was extensively recrystallized, with concordant dates that span from c. 610–500 Ma, and retain only vestigial cores. Monazite cores yield dates that overlap with the garnet Lu–Hf dates and typically have low‐Y and heavy rare earth element (HREE) concentrations, corroborating interpretations of low‐Y and low‐HREE monazite domains as records of synchronous garnet growth. However, ratios of REE concentrations in garnet and monazite do not consistently match previously reported partition coefficients for the REE between these two minerals. High‐Y monazite inclusions within pristine, crack‐free garnet yield U–Pb dates significantly younger than the Lu–Hf dates for the same samples, indicating recrystallization of monazite within garnet. The recrystallization of high‐Y and high‐HREE monazite domains over >50 Ma likely records either punctuated thermal pulses or prolonged residence at relatively high temperatures (up to ~610–680 °C) driving monazite recrystallization. One c. 616 Ma garnet Lu–Hf date and several c. 610–600 Ma monazite U–Pb dates are tentatively interpreted as records of the onset of tectonism metamorphism in the Ross orogeny, with a more robust constraint from the other Lu–Hf dates (c. 588–572 Ma) and numerous c. 590–570 Ma monazite U–Pb dates. The data are consistent with a tectonic model that involves shortening and thickening prior to widespread magmatism in the vicinity of the study area. The early tectonic history of the Ross orogen, recorded in metamorphic rocks, was broadly synchronous with Gondwana‐wide collisional Pan‐African orogenies.     

Coupling thermodynamic modeling and high-resolution in situ LA-ICP-MS monazite geochronology: evidence for Barrovian metamorphism late in the Grenvillian history of southeastern Ontario

The Flinton Group is a greenschist to upper amphibolite facies package of metasediments in southeastern Ontario that was metamorphosed during the Ottawan Orogeny. Thermodynamic modeling of metapelitic mineral assemblages suggests an increase in peak conditions of metamorphism across the 40 km wide study area from 3.5 to 7.9 kbar and 540 to 715 °C. Garnet isopleth thermobarometry applied to the cores of compositionally zoned porphyroblasts reveals remarkably similar P-T conditions of initial crystallization at approximately 3.7–4.0 kbar and 512–520 °C, corresponding to a relatively high geothermal gradient of ca. 34–45 °C km^?1. It is inferred from modeling and reaction textures that metamorphism was along Barrovian P-T paths. Major and trace element zoning in garnet from one sample records a complex growth history as evidenced by major and trace element zoning and the distribution of xenotime, allanite and monazite inclusions. High-resolution (6 μm) LA-ICP-MS U-Pb geochronology performed on monazite in the rock matrix and included in the outer 150 μm of garnet rim-ward of a Y annulus revealed an age of 976?±?4 Ma. The age is interpreted to reflect monazite growth at the expense of allanite and apatite late in garnet’s growth history over the P-T interval 4.5–6.8 kbar and 540–640 °C. This new age estimate for near peak metamorphism fits well into the regional framework but is significantly younger than previously reported ages for Ottawan metamorphism. Based on microstructures this new age suggests that compressional tectonics were operating much later in the history of the Grenville of southeastern Ontario than previously thought.     

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

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

The timing of migmatization in the northern Arabian–Nubian Shield: Evidence for a juvenile sedimentary component in collision‐related batholiths

Collision‐related granitoid batholiths, like those of the Hercynian and Himalayan orogens, are mostly fed by magma derived from metasedimentary sources. However, in the late Neoproterozoic calcalkaline (CA) batholiths of the Arabian–Nubian Shield (ANS), which constitutes the northern half of the East African orogen, any sedimentary contribution is obscured by the juvenile character of the crust and the scarcity of migmatites. Here, we use paired in situ LASS‐ICP‐MS measurements of U–Th–Pb isotope ratios and REE contents of monazite and xenotime and SHRIMP‐RG analyses of separated zircon to demonstrate direct linkage between migmatites and granites in the northernmost ANS. Our results indicate a single prolonged period of monazite growth at 640–600 Ma, in metapelites, migmatites and peraluminous granites of three metamorphic suites: Abu‐Barqa (SW Jordan), Roded (S Israel) and Taba–Nuweiba (Sinai, Egypt). The distribution of monazite dates and age zoning in single monazite grains in migmatites suggest that peak thermal conditions, involving partial melting, prevailed for c. 10 Ma, from 620 to 610 Ma. REE abundances in monazite are well correlated with age, recording garnet growth and garnet breakdown in association with the prograde and retrograde stages of the melting reactions, respectively. Xenotime dates cluster at 600–580 Ma, recording retrogression to greenschist facies conditions as garnet continued to destabilize. Phase equilibrium modelling and mineral thermobarometry yield P–T conditions of ~650–680°C and 5–7 kbar, consistent with either water‐fluxed or muscovite‐breakdown melting. The expected melt production is 8–10 vol.%, allowing a melt connectivity network to form leading to melt segregation and extraction. U–Pb ages of zircon rims from leucosomes indicate crystallization of melt at 610 ± 10 Ma, coinciding with the emplacement of a vast volume of CA granites throughout the northern ANS, which were previously considered post‐collisional. Similar monazite ages (c. 620 Ma) retrieved from the amphibolite facies Elat schist indicate that migmatites are the result of widespread regional rather than local contact metamorphism, representing the climax of the East African orogenesis.     

Age and duration of ultrahigh-temperature metamorphism in the Anápolis–Itauçu Complex, Southern Brasília Belt, central Brazil – constraints from U–Pb geochronology, mineral rare earth element chemistry and trace-element thermometry

Integrated petrographic and chemical analysis of zircon, garnet and rutile from ultrahigh‐temperature (UHT) granulites in the Anápolis–Itauçu Complex, Brazil, is used to constrain the significance of zircon ID‐TIMS U–Pb geochronological data. Chondrite‐normalized rare earth element (REE) profiles of zircon cores have positive‐sloping heavy‐REE patterns, commonly inferred to be magmatic, whereas unambiguous metamorphic grains and overgrowths have flat to slightly negatively sloping heavy‐REE patterns. However, in one sample, a core of zircon interpreted as having formed prior to garnet crystallization and a metamorphic zircon formed within microstructures involving garnet breakdown both display elevated heavy‐REE (and Y) with positive‐sloping patterns. D_REE(zrc/grt) partition coefficients suggest an approximation to equilibrium between zircon and garnet cores, although progressive enrichment in heavy REE towards garnet rims occurs in two of the samples investigated. Titanium‐in‐zircon thermometry indicates zircon growth during both the prograde and post‐peak evolution, but not at peak temperatures of the UHT metamorphism. By contrast, zirconium‐in‐rutile thermometry of inclusions armoured by garnet records crystallization temperatures, based on the upper end of the interquartile range of the data, of ～890 to 870 °C and maximum temperature around 980 °C, indicating prograde and retrograde growth close to and after peak conditions. Rutile located in retrograde microstructures records crystallization temperatures of 850 to 820 °C. Rutile intergrown with ilmenite and included within orthopyroxene, which is associated with exsolved zircon, records temperatures ～760 °C, consistent with Ti‐in‐zircon crystallization temperatures. ID‐TIMS U–Pb geochronological data from two of the four samples investigated define upper intercept ages of 641.3 ± 8.4 Ma (MSWD 0.91) and 638.8 ± 2.5 Ma (MSWD 1.03) that correlate with periods of zircon growth along the prograde segment of the P–T path. Individual zircon U–Pb dates retrieved from all samples range from 649 to 634 Ma, indicating a maximum duration of c. 15 Myr for the UHT event. This period is interpreted as recording modest thickening of hot backarc lithosphere located behind the Arenópolis Arc at the edge of the São Francisco Craton consequent upon terminal collision of the Parána Block with the arc during the amalgamation of West Gondwana.