Abstract
AbstractMonazite is a common accessory phase in felsic granulite ribbon mylonites exposed in the Upper Deck domain of the Athabasca granulite terrane, western Canadian Shield. Field relationships, bulk rock geochemistry and phase equilibria modelling in the Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–Fe2O3 system are consistent with the garnet‐rich rocks representing the residual products of ultrahigh temperature melting of biotite‐bearing paragneisses driven by intraplating of mafic magma in continental lower crust. The c. 2.64–2.61 Ga Y‐rich resorbed monazite cores included in garnet are interpreted as relicts of detrital grains deposited on the Earth's surface after c. 2.61 Ga. Yttrium‐poor monazite domains in garnet are depleted in Sm and Gd and linked to fluid‐absent melting of biotite + plagioclase + quartz ± sillimanite during a prograde loading path from ≤0.8 to ≥1.4 GPa. The c. 2.61–2.55 Ga Y‐depleted, Th‐rich monazite domains crystallized in the presence of garnet + ternary feldspar ± orthopyroxene + peraluminous melt. The c. 2.58–2.52 Ga monazite rims depleted in Th + Ca and enriched in Eu are linked to localized melt extraction synchronous with growth of high‐pressure (HP) grossular‐rich garnet at the expense of plagioclase during crustal thickening, culminating at >950 °C. Re‐heating and dextral transpressive lower crustal reactivation at c. 1.9 Ga resulted in syn‐kinematic growth of (La + Ce)‐enriched monazite and a second generation of garnet, concurrent with recrystallization of feldspar and orthopyroxene at 1.0–1.2 GPa and 600–700 °C. Monazite grains in this study are marked by positive Eu‐anomalies relative to chondrite. A direct link is implied between Y, Sm, Eu and Gd in monazite and two major phases in continental lower crust: garnet and plagioclase. Positive Eu‐anomalies in lower crustal monazite associated with modally abundant garnet appear to be directly related to Eu‐enrichment and depletions of Y, Sm and Gd that are consequences of garnet growth and plagioclase breakdown during HP melting of peraluminous bulk compositions.
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