4.5 Article

Dehydration of Glaucophane in the System Na2O-MgO-Al2O3-SiO2-H2O and the Effects of NaCl-, CO2- and Silicate-bearing Aqueous Fluids

Journal

JOURNAL OF PETROLOGY
Volume 60, Issue 12, Pages 2369-2385

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/petrology/egaa011

Keywords

blueschist; dehydration; glaucophane; pyroxene solid solution; silicate-bearing aqueous fluids

Funding

  1. NSF [EAR-1725053]

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Arc magmas are thought to be generated by partial melting of the mantle wedge above the subduction slab, which is triggered by the fluids from the dehydration of subducting oceanic crust. Among the dehydration reactions, those occurring at the depths of the blueschist-to-eclogite transition are considered to be very important. The sodium amphibole glaucophane (square Na2Mg3Al2Si8O22(OH)(2), where square represents a vacancy) is characteristic of blueschists, so that determining the higher-temperature stability of end-member glaucophane helps constrain the maximum temperature of the transition between blueschists and eclogites. A reversed determination of the dehydration reaction 2 glaucophane = 4 jadeite + 3 enstatite + 2 quartz + 2 H2O was done in the system Na2O-MgO-Al2O3-SiO2-H2O over the pressure-temperature (P-7) range of 2.5-3.3 GPa and 760-900 degrees C for durations of 24-96 hours, using synthetic phases as starting materials. The reaction was bracketed at 830-850 degrees C at 2.5 GPa and at 810-830 degrees C at 2.9 GPa in the presence of water. In addition to pure water, 5 molality H2O-NaCl (mole fraction X-Nacl = 0.08) and 5 molality H2O-CO2 (XCO2 = 0.08) fluids were used to check the effects of NaCl and CO2, respectively, on the dehydration reaction. The H2O-NaCl fluid shifts the reaction boundary at 2.5 GPa from 840 degrees C to a lower T (800 degrees C), while the CO2-H2O fluid shifts the boundary to a higher T (860 degrees C). At these high P-Tconditions, the fluid, even without any added NaCl or CO2, is a silicate-bearing aqueous fluid. The different effects of NaCl and CO2 are attributed to differences in their capabilities to inhibit the solubility of silicates, such as quartz in water, and in changing the activity of water at such P-Tconditions. The difference can shift the depth of dehydration by 6 km for an average low d T/dP geothermal gradient of 325 degrees C/GPa. The shift in the boundary could be considerably larger for shallower d T/dP slab-top geothermal gradients. The experimental results show a good fit with those from thermodynamic modelling and aqueous geochemical calculation.

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