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The bulk density of a planet, as measured by mass and radius, is a result of planet structure and composition. Relative proportions of iron core, rocky mantle, and gaseous envelopes are degenerate for a given density. This degeneracy is reduced for rocky planets without significant gaseous envelopes when the structure is assumed to be a differentiated iron core and rocky mantle, in which the core mass fraction (CMF) is a first-order description of a planet’s bulk composition. A rocky planet’s CMF may be derived both from bulk density and by assuming the planet reflects the host star’s major rock-building elemental abundances (Fe, Mg, and Si). Contrasting CMF measures, therefore, shed light on the outcome diversity of planet formation from processes including mantle stripping, out-gassing, and/or late-stage volatile delivery. We present a statistically rigorous analysis of the consistency of these two CMF measures accounting for observational uncertainties of planet mass and radius and host-star chemical abundances. We find that these two measures are unlikely to be resolvable as statistically different unless the bulk density CMF is at least 40% greater than or 50% less than the CMF as inferred from the host star. Applied to 11 probable rocky exoplanets, Kepler-107 c has a CMF as inferred from bulk density that is significantly greater than the inferred CMF from its host star (2σ) and is therefore likely an iron-enriched super-Mercury. K2-229b, previously described as a super-Mercury, however, does not meet the threshold for a super-Mercury at a 1σor 2σlevel.

 

The degree to which the Earth’s mantle stores and cycles water in excess of the storage capacity of nominally anhydrous minerals is dependent upon the stability of hydrous phases under mantle-relevant pressures, temperatures, and compositions. Two hydrous phases, phase D and phase H, are stable to the pressures and temperatures of the Earth’s lower mantle, suggesting that the Earth’s lower mantle may participate in the cycling of water. We build on our prior work of density functional theory calculations on phase H with the stability, structure, and bonding of hydrous phases D, and we predict the aluminum partitioning with H in the Al 2 O 3 -SiO 2 -MgO-H 2 O system. We address the solid solutions through a statistical sampling of site occupancy and calculation of the partition function from the grand canonical ensemble. We show that each phase has a wide solid solution series between MgSi 2 O 6 H 2 -Al 2 SiO 6 H 2 and MgSiO 4 H 2 -2 δ AlOOH + SiO 2 , in which phase H is more aluminum rich than phase D at a given bulk composition. We predict that the addition of Al to both phases D and H stabilizes each phase to higher temperatures through additional configurational entropy. While we have shown that phase H does not exhibit symmetric hydrogen bonding at high pressure, we report here that phase D undergoes a gradual increase in the number of symmetric H-bonds beginning at ∼30 GPa, and it is only ∼50% complete at 60 GPa.