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    New mineral activity-composition relations for thermodynamic calculations in metapelitic systems
    White, RW ; Powell, R ; Holland, TJB ; Johnson, TE ; Green, ECR (WILEY-BLACKWELL, 2014-04)
    Abstract New activity–composition (a–x) relations for minerals commonly occurring in metapelites are presented for use with the internally consistent thermodynamic dataset of Holland & Powell (, Journal of Metamorphic Geology, 29, 333–383). The a–x relations include a broader consideration of Fe2O3 in minerals, changes to the formalism of several phases and order–disorder in all ferromagnesian minerals where Fe–Mg mixing occurs on multiple sites. The a–x relations for chlorite, biotite, garnet, chloritoid, staurolite, cordierite, orthopyroxene, muscovite, paragonite and margarite have been substantially reparameterized using the approach outlined in the companion paper in this issue. For the first time, the entire set of a–x relations for the common ferromagnesian minerals in metapelitic rocks is parameterized simultaneously, with attention paid to ensuring that they can be used together to calculate phase diagrams of geologically appropriate topology. The a–x relations developed are for use in the Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–O2 (NCKFMASHTO) system for both subsolidus and suprasolidus conditions. Petrogenetic grids in KFMASH and KFMASHTO are similar in topology to those produced with earlier end‐member datasets and a–x relations, but with some notable differences. In particular, in subsolidus equilibria, the FeO/(FeO + MgO) of garnet is now greater than in coexisting staurolite, bringing a number of key staurolite‐bearing equilibria into better agreement with inferences from field and petrographic observations. Furthermore, the addition of Fe3+ and Ti to a number of silicate phases allows more plausible equilibria to be calculated in relevant systems. Pseudosections calculated with the new a–x relations are also topologically similar to equivalent diagrams using earlier a–x relations, although with many low variance fields shifting in P–T space to somewhat lower pressure conditions.
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    The effect of Mn on mineral stability in metapelites revisited: new a-x relations for manganese-bearing minerals
    White, RW ; Powell, R ; Johnson, TE (WILEY, 2014-10)
    Abstract The a–x relations recently presented in White et al. (, Journal of Metamorphic Geology, 32, 261–286) are extended to include MnO. This provides a set of internally consistent a–x relations for metapelitic rocks in the MnO–Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–O2 (MnNCKFMASHTO) system. The mixing parameters for the Mn‐bearing minerals were estimated using the micro‐ϕ approach of Powell et al. (, Journal of Metamorphic Geology, 32, 245–260). Then the Mn‐end‐member thermodynamic properties were calibrated using a database of co‐existing minerals involving literature data from rocks and from experiments on natural materials. Mn‐end‐members were calibrated for orthopyroxene, cordierite, staurolite, chloritoid, chlorite, biotite, ilmenite and hematite, assuming known properties for the garnet end‐member spessartine. The addition of MnO to phase diagram calculations results in a marked expansion of the stability of garnet‐bearing assemblages. At greenschist facies conditions garnet stability is extended down temperature. At amphibolite facies conditions, the garnet‐in boundary shifts to lower pressure. While the addition of MnO greatly influences the stability of garnet, it has relatively little effect on the stability of other common metapelitic minerals, with the resultant diagrams being topologically very similar to those calculated without MnO. Furthermore, the addition of MnO in the amounts measured in most metapelites has only a small effect on the mode of garnet, with calculated garnet modes remaining smaller than 1% in the P–T range outside its predicted Mn‐free P–T range.
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    Grain-scale pressure variations and chemical equilibrium in high-grade metamorphic rocks
    Tajcmanova, L ; Podladchikov, Y ; Powell, R ; Moulas, E ; Vrijmoed, JC ; Connolly, JAD (WILEY, 2014-02)
    Abstract In the classical view of metamorphic microstructures, fast viscous relaxation (and so constant pressure) is assumed, with diffusion being the limiting factor in equilibration. This contribution is focused on the only other possible scenario – fast diffusion and slow viscous relaxation – and brings an alternative interpretation of microstructures typical of high‐grade metamorphic rocks. In contrast to the pressure vessel mechanical model applied to pressure variation associated with coesite inclusions in various host minerals, a multi‐anvil mechanical model is proposed in which strong single crystals and weak grain boundaries can maintain pressure variation at geological time‐scales in a polycrystalline material. In such a mechanical context, exsolution lamellae in feldspar are used to show that feldspar can sustain large differential stresses (>10 kbar) at geological time‐scales. Furthermore, it is argued that the existence of grain‐scale pressure gradients combined with diffusional equilibrium may explain chemical zoning preserved in reaction rims. Assuming zero net flux across the microstructure, an equilibrium thermodynamic method is introduced for inferring pressure variation corresponding to the chemical zoning. This new barometric method is applied to plagioclase rims around kyanite in felsic granulite (Bohemian Massif, Czech Republic), yielding a grain‐scale pressure variation of 8 kbar. In this approach, kinetic factors are not invoked to account for mineral composition zoning preserved in rocks metamorphosed at high grade.
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    Rare eclogite-mafic granulite in felsic granulite in Blansk y les: precursor of intermediate granulite in the Bohemian Massif?
    Stipska, P ; Powell, R ; Racek, M (WILEY, 2014-05)
    Abstract Mafic granulite, generated from eclogite, occurs in felsic granulite at Kleť, Blanský les, in the Bohemian Massif. This is significant because such eclogite is very rare within the felsic granulite massifs. Moreover, at this locality, strong interaction has occurred between the mafic granulite and the adjacent felsic granulite producing intermediate granulite, such intermediate granulite being of enigmatic origin elsewhere. The mafic granulite involves garnet from the original eclogite, containing large idiomorphic inclusions of omphacite, plagioclase and quartz, as well as rutile. The edge of the garnet is replaced by a plagioclase corona, with the garnet zoned towards the corona and also the inclusions. The original omphacite–quartz–?plagioclase matrix has recrystallized to coarse‐grained polygonal (‘equilibrium’‐textured) plagioclase‐diopsidic clinopyroxene–orthopyroxene also with brown amphibole commonly in the vicinity of garnet. Somewhat larger quartz grains are embedded in this matrix, along with minor ilmenite, rutile and zircon. Combining the core garnet composition with core inclusion compositions gives a pressure of the order of 18 kbar from assemblage and isopleths on a P−T pseudosection, with temperature poorly constrained, but most likely >900 °C. From this P−T pseudosection, the recrystallization of the matrix took place at ~12 kbar, and from Zr‐in‐rutile thermometry, at relatively hot conditions of 900–950 °C. It is largely at these conditions that the eclogite/mafic granulite interacted with the felsic granulite to make intermediate granulite (see next paper).
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    HIGH-PRESSURE METAMORPHISM OF SERPENTINIZED CHROMITITE AT LUOBUSHA (SOUTHERN TIBET)
    Huang, M-X ; Yang, J-J ; Powell, R ; Mo, X (AMER JOURNAL SCIENCE, 2014-01)
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