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Journal ArticleDOI

Retrograde processes in migmatites and granulites revisited

TLDR
In this article, the authors show that the extent of post-thermal peak reaction is influenced by several factors, including the P-T path in relation to invariants in the system and the Clapeyron slopes of the equilibria, and the availability of fluid (H2O-rich volatile phase or melt) for fluid-consuming reactions.
Abstract
Many migmatites and granulites preserve evidence of a clockwise P–T evolution involving decompression (decrease in P) while close to the thermal peak The extent of post-thermal peak reaction is influenced by several factors, including: (1) the P–T path in relation to invariants in the system and the Clapeyron slopes of the equilibria; (2) the rate of cooling; and (3) the availability of fluid (H2O-rich volatile phase or melt) for fluid-consuming reactions Reaction may occur between products of a prograde (increasing T) fluid-generating reaction as the same equilibrium is re-crossed in the retrograde (decreasing T) sense In general, reaction reversal or ‘back reaction’ requires the P–T path to approximate isobaric heating and cooling, without significant decompression, and evolved fluid to remain within the equilibration volume The larger the decompression segment in the P–T evolution, the more chance there is of crossing different reactions along the retrograde segment from those crossed along the prograde segment For common pelite compositions, we may generalize by considering three pressure regimes separated by the [Spl, Ms, H2O] invariant in KFMASH (approximately 9 kbar) and the intersection of muscovite breakdown with the H2O-rich volatile phase-saturated solidus (approximately 4 kbar) Reaction reversal cannot occur along P–T paths that traverse around one of these points, but may occur along P–T paths confined to one of the three regimes in between Additionally, above the solidus, melt segregation and loss potentially change the composition of the equilibration volume; and, the size of the equilibration volume shrinks with decreasing T Since the proportion of melt to residue in the equilibration volume may change with decreasing size, the composition of the equilibration volume may change throughout the supra-solidus part of the retrograde segment of the P–T evolution If melt has been lost from the equilibration volume, reaction reversal may not be possible or may be only partial; indeed, the common preservation of close-to-peak mineral assemblages in migmatite and granulite demonstrates that extensive reaction with melt is uncommon, which implies melt isolation or loss prior to crossing potential melt-consuming reactions Water dissolved in melt is transported through the crust to be exsolved on crystallization at the solidus appropriate to the intrinsic a(H2O) This recycled water causes retrogression at subsolidus conditions Consideration of the evidence for supra-solidus decompression-dehydration reactions, and review of microstructures that have proven controversial, such as corona and related microstructures, selvage microstructures and ‘late’ muscovite, leads to the conclusion that there is more than one way for these microstructures to form and reminds us that we should always consider multiple working hypotheses!

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Citations
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Journal ArticleDOI

The Ti-saturation surface for low-to-medium pressure metapelitic biotites: Implications for geothermometry and Ti-substitution mechanisms

TL;DR: The relationship between Ti-content, temperature, and Mg/(Mg + Fe) value was calibrated empirically using an extensive natural biotite data set (529 samples) from western Maine and south-central Massachusetts in combination with the petrogenetic grid of Spear et al..
Journal ArticleDOI

Metamorphic Conditions in Orogenic Belts: A Record of Secular Change

TL;DR: The abundance and scale of ultra-high-temperature (UHT) metamorphic belts from the Neoarchean to the Cambrian imply a significant change in geodynamics during the Neo-Archean Era, after which transient sites of high heat flow were available at intervals throughout this period of Earth evolution as mentioned in this paper.
Book

A Practical Guide to Rock Microstructure

TL;DR: In this article, a glossary of microstructural terms for sedimentary and metamorphic rocks is presented, along with a discussion of the relationship between sedimentary, igneous and deformed rocks.
Journal ArticleDOI

Melt loss and the preservation of granulite facies mineral assemblages

TL;DR: In this article, phase diagram modelling of the effects of melt loss in hypothetical aluminous and subaluminous metapelitic compositions is presented, showing that the amount of melt that has to be removed from a rock to preserve a granulite facies assemblage varies markedly with rock composition, the number of partial melt loss events and the P-T conditions at which melt loss occurs.
Journal ArticleDOI

Granite: From genesis to emplacement

TL;DR: In this paper, phase diagrams for pelite are used to illustrate the mineralogical controls on melt production and the consequences of different clockwise pressure-temperature (P - T ) paths on melt composition.
References
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Journal ArticleDOI

An internally consistent thermodynamic data set for phases of petrological interest

TL;DR: In this paper, the thermodynamic properties of 154 mineral endmembers, 13 silicate liquid end-members and 22 aqueous fluid species are presented in a revised and updated data set.
Journal ArticleDOI

The origins of granulites: a metamorphic perspective

TL;DR: A thorough survey of over 90 granulite terranes or occurrences reveals that over 50% of them record P-T conditions outside the 7.5 ± 1 kbar and 800 ± 50 °C average granulites regime preferred by many authors as discussed by the authors.
Journal ArticleDOI

Calculating phase diagrams involving solid solutions via non‐linear equations, with examples using THERMOCALC

TL;DR: The THERMOCALC software as mentioned in this paper allows the calculation of a range of other types of phase diagrams involving solid solutions, such as P-T projections and compatibility diagrams, with the equations used for each equilibrium are the equilibrium relationships for an independent set of reactions between the endmembers of the phases in the equilibrium.
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