4.6 Article

Diamond resorption and immiscibility of C-O-H fluid in kimberlites: Evidence from experiments in H2O - CO2 - SiO2 - MgO - CaO system at 1-3 GPa

Journal

LITHOS
Volume 380, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.lithos.2020.105858

Keywords

Kimberlitic fluid; Immiscible C-O-H fluids; Diamond resorption features; High-pressure experiment; Synthetic fluid inclusion technique; Atomic force microscope

Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)

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This study conducted experiments under kimberlite ascent conditions to examine the relationship between the H2O:CO2 ratio of the fluid and diamond resorption, finding that the morphology of diamond resorption depends on the proportions of end-member aqueous and carbonic fluids. This suggests that the bulk composition of the fluid plays a role in determining diamond resorption characteristics.
Kimberlites are the deepest sourced magmas emplaced at the Earth's surface. They provide a window into the processes at the base of the subcratonic mantle. A better understanding of the origin, composition, and emplacement mechanisms of kimberlites is hampered by uncertainties in the contents of the two main volatiles, H2O and CO2. Diamond dissolution in H2O and in CO2 fluids produces distinct resorption features offering an opportunity to determine the composition of the magmatic fluid in kimberlites. Here we examined the relationship between H2O:CO2 ratio of the fluid and the style of diamond resorption by conducting experiments in C-O-H fluid saturated with silicates with variable H2O:CO2 ratios at the conditions of kimberlite ascent of 1-3 GPa and 1150-1350 degrees C. Our results showed that the geometry of etch pits on diamond and the resorption style evolve consistently as bulk CO2 content of the fluid changes from 0 to 50 to 50-90 and 90-100 mol%. The fluid composition at the run conditions was monitored by entrapment of synthetic fluid inclusions in olivine and quartz. The inclusions demonstrated the existence of a fluid miscibility gap at 1-3 GPa and 1250 degrees C with two fluid endmembers, an aqueous and a carbonic phase, which H2O:CO2 ratio at 1 GPa determined with confocal Raman microscopy is (H2O)0.62(CO2)0.38 and (H2O)0.12(CO2)0.88 respectively. Hence, diamond resorption morphology depends on the proportions of the end-member aqueous and carbonic fluids, which vary with the bulk composition of the fluid. The different density and ability of aqueous and carbonic fluids to dissolve silicates (olivine) would promote their separation in the rising magma column. Concentration of the lower density aqueous fluid towards the tip of the propagating dyke would facilitate more efflcient fracturing of the country rocks and faster ascent of the kimberlite magma causing explosive eruption. We propose that preferential attachment of aqueous fluid bubbles would help to increase the buoyancy of olivine xenocrysts and possibly diamond in the kimberlite magma offering a mechanism for transporting the heavy mantle cargo. (c) 2020 Elsevier B.V. All rights reserved.

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