Abstract The interpretation of metamorphic ages for zircon domains in eclogite remains challenging because of the uncertainties in interpreting their rare earth element (REE) patterns and mineral inclusions. This has seriously hindered the construction of robust pressure ( P )–temperature ( T )–time ( t ) paths for eclogites from collisional orogens. In this study, a composite approach is used to obtain a reliable P–T path for eclogite from the Tongbai orogen and quantitatively attribute zircon U–Pb ages to specific P–T intervals. An integrated study using isochemical phase diagram section (pseudosection) modelling, multi‐equilibrium thermobarometry, and the Zr‐in‐rutile thermometry with petrographic observations indicates that the target eclogite experienced multistage metamorphic evolution. The evolution is characterized by a clockwise P–T path with compressional heating for peak eclogite facies metamorphism at 588 ± 20°C and 26.7 ± 2.8 kbar and two stages of isothermal decompression from an early stage of amphibole eclogite facies metamorphism at 15–10 kbar to a late stage of amphibolite facies metamorphism at pressures of <10 kbar. Metamorphic zircon domains in eclogite and quartz vein show relatively flat patterns of heavy REE without notable Eu anomalies but different cathodoluminescence responses and middle REE (MREE) contents. This indicates their growth in different stages of eclogite facies metamorphism, which are categorized into two groups. The first group is composed of bright rims or homogenous grains that are characterized by low MREE contents, suggesting the existence of abundant amphibole during the metamorphism. The compositional isopleths of amphibole inclusions indicate that this group of zircon domains would form by hydration during crustal exhumation to amphibole eclogite facies at 240 ± 2 Ma. The second group consists of dark sector mantles and shows high MREE contents, indicating the prograde to peak metamorphism with significant decomposition of amphibole or lawsonite during crustal subduction to eclogite facies at 245 ± 2 Ma. Therefore, the combination of the isopleth thermobarometry of mineral inclusions with the Zr‐in‐rutile thermometry and the zircon REE partitioning is an effective means to link the metamorphic P–T conditions to the ages of metamorphic zircons in the different stages of collisional orogeny.
Abstract Several types of multiphase solid (MS) inclusions are identified in garnet from ultrahigh‐pressure (UHP) eclogite in the Dabie orogen. The mineralogy of MS inclusions ranges from pure K‐feldspar to pure quartz, with predominance of intermediate types consisting of K‐feldspar + quartz ± silicate (plagioclase or epidote) ± barite. The typical MS inclusions are usually surrounded with radial cracks in the host garnet, similar to where garnet contains relict coesite. Barite aggregates display significant heterogeneity in major element composition, with total contents of only 57–73% and highly variable SiO 2 contents of 0.32–25.85% that are positively correlated with BaO and SO 3 contents. The occurrence of MS inclusions provides petrographic evidence for partial melting in the UHP metamorphic rock. The occurrence of barite aggregates with variably high SiO 2 contents suggests the coexistence of aqueous fluid with hydrous melt under HP eclogite facies conditions. Thus, local dehydration melting is inferred to take place inside the UHP metamorphic slice during continental collision. This is ascribed to phengite breakdown during ‘hot’ exhumation of the deeply subducted continental crust. As a consequence, the aqueous fluid is internally buffered in chemical composition and its local sink is a basic trigger to the partial melting during the continental subduction‐zone metamorphism.
Abstract Composite multiphase solid ( MS ) inclusions composed of carbonate and silicate minerals have been found for the first time in metamorphic garnet from ultrahigh‐ P eclogite from the Dabie orogen. These inclusions are morphologically euhedral to subhedral, and some show relatively regular shapes approaching the negative crystal shape of the host garnet. Radial fractures often occur in garnet hosting the inclusions. The inclusions are primarily composed of variable proportions of carbonate and silicate minerals such as calcite, quartz, K‐feldspar and plagioclase, with occasional occurrences of magnetite, zircon and barite. They are categorized into two groups based on the proportions of carbonate and silicate phases. Group I is carbonate‐dominated with variable proportions of silicate minerals, whereas Group II is silicate‐dominated with small proportions of carbonates. Trace element analysis by LA ‐ ICPMS for the two groups of MS inclusions yields remarkable differences. Group I inclusions exhibit remarkably lower REE contents than Group II inclusions, with significant LREE enrichment and large fractionation between LREE and HREE in the chondrite‐normalized REE diagram. In contrast, Group II inclusions show rather flat REE patterns with insignificant fractionation between LREE and HREE . In the primitive mantle‐normalized spidergram, Group I inclusions exhibit positive anomalies of Zr and Hf, whereas Group II inclusions show negative anomalies of Zr and Hf. Nevertheless, both groups exhibit positive anomalies of Ba, U, Pb and Sr, but negative anomalies of Nb and Ta, resembling the composition of common continental crust. Group I inclusions have higher Ba and U contents than Group II inclusions. Combined with petrological observations, the two groups of MS inclusions are interpreted as having crystallized from composite silicate and carbonate melts during continental subduction‐zone metamorphism. The differences in trace element composition between the two groups are primarily attributed to the proportions of carbonate and silicate phases in the MS inclusions. The silicate melts were derived from the breakdown of hydrous minerals such as paragonite and phengite, whereas the occurrence of carbonate melts indicates involvement of carbonate minerals in the partial melting and thus has great bearing on recycling of supracrustal carbon into the mantle. The coexistence of silicate and carbonate melts in the eclogitic garnet provides insights into the nature of hydrous melts in the subduction factory.
ABSTRACT An integrated study of U–Pb ages and trace elements was carried out for titanite and zircon from ultrahigh‐pressure (UHP) metagranites in the Sulu orogen, east‐central China. The results provide constraints on the composition of metamorphic fluids during the exhumation of deeply subducted continental crust. Titanite has two domain types based on REE patterns and trace element variations, Ttn‐I and Ttn‐II respectively. These two domains show indistinguishable U–Pb ages of 232 ± 14 to 220 ± 8 Ma, in general agreement with anatectic zircon U–Pb ages of 223 ± 4 to 219 ± 2 Ma for the partial melting event during early exhumation. The Ttn‐I domains have significantly higher REE, Th, Ta and Sr, and higher Th/U ratios than the Ttn‐II domains, indicating that the two domains have grown from metamorphic fluids with different compositions. For the Ttn‐I domains, Zr‐in‐titanite thermometry yields high temperatures of 773–851 °C at 2.5 GPa, and petrographic observations reveal the presence of melt pseudomorphs. Thus, they are interpreted to have grown from hydrous melts in the early exhumation stage. In contrast, the Ttn‐II domains were texturally equilibrated with amphibolite facies minerals such as biotite and plagioclase and contain inclusions of plagioclase and quartz. The Zr‐in‐titanite thermometry yields lower temperatures of 627–685 °C at 1.0 GPa. In combination with their REE patterns, they are interpreted to have grown from aqueous solutions at amphibolite facies metamorphic conditions during further exhumation. The differences in Th and Sr contents are prominent between the Ttn‐I and Ttn‐II domains, signifying the compositional difference between the hydrous melts and aqueous solutions. Therefore, the polygenetic titanite in the UHP metamorphic rocks provides insights into the geochemical property of metamorphic fluids during the continental subduction‐zone processes.
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