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[1] The recent determination of the gravity field of Mercury and new Earth-based radar observations of the planet's spin state afford the opportunity to explore Mercury's internal structure. These observations provide estimates of two measures of the radial mass distribution of Mercury: the normalized polar moment of inertia and the fractional polar moment of inertia of the solid portion of the planet overlying the liquid core. Employing Monte Carlo techniques, we calculate several million models of the radial density structure of Mercury consistent with its radius and bulk density and constrained by these moment of inertia parameters. We estimate that the top of the liquid core is at a radius of 2020 AE 30 km, the mean density above this boundary is 3380 AE 200 kg m À3 , and the density below the boundary is 6980 AE 280 kg m À3 . We find that these internal structure parameters are robust across a broad range of compositional models for the core and planet as a whole. Geochemical observations of Mercury's surface by MESSENGER indicate a chemically reducing environment that would favor the partitioning of silicon or both silicon and sulfur into the metallic core during core-mantle differentiation. For a core composed of Fe-S-Si materials, the thermodynamic properties at elevated pressures and temperatures suggest that an FeS-rich layer could form at the top of the core and that a portion of it may be presently solid.

Abstract-We studied 26 IAB iron meteorites containing silicate-bearing inclusions to better constrain the many diverse hypotheses for the formation of this complex group. These meteorites contain inclusions that fall broadly into five types: (1) sulfide-rich, composed primarily of troilite and containing abundant embedded silicates; (2) nonchondritic, silicate-rich, comprised of basaltic, troctolitic, and peridotitic mineralogies; (3) angular, chondritic silicate-rich, the most common type, with approximately chondritic mineralogy and most closely resembling the winonaites in composition and texture; (4) rounded, often graphite-rich assemblages that sometimes contain silicates; and ( 5 ) phosphate-bearing inclusions with phosphates generally found in contact with the metallic host. Similarities in mineralogy and mineral and 0-isotopic compositions suggest that IAB iron and winonaite meteorites are from the same parent body.We propose a hypothesis for the origin of IAB iron meteorites that combines some aspects of previous formation models for these meteorites. We suggest that the precursor parent body was chondritic, although unlike any known chondrite group. Metamorphism, partial melting, and incomplete differentiation (i.e., incomplete separation of melt from residue) produced metallic, sulfide-rich and silicate partial melts (portions of which may have crystallized prior to the mixing event), as well as metamorphosed chondritic materials and residues. Catastrophic impact breakup and reassembly of the debris while near the peak temperature mixed materials fiom various depths into the re-accreted parent body. Thus, molten metal from depth was mixed with near-surface silicate rock, resulting in the formation of silicate-rich IAB iron and winonaite meteorites. Results of smoothed particle hydrodynamic model calculations support the feasibility of such a mixing mechanism. Not all of the metal melt bodies were mixed with silicate materials during this impact and reaccretion event, and these are now represented by silicate-free IAB iron meteorites. Ages of silicate inclusions and winonaites of 4. 40-4.54 Ga indicate this entire process occurred early in solar system history.

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[1] The Mars Exploration Rover Spirit analyzed multiple occurrences of sulfur-rich, lighttoned soils along its traverse within Gusev Crater. These hydrated deposits are not readily apparent in images of undisturbed soil but are present at shallow depths and were exposed by the actions of the rover wheels. Referred to as ''Paso Robles'' class soils, they are dominated by ferric iron sulfates, silica, and Mg-sulfates. Ca-sulfates, Ca-phosphates, and other minor phases are also indicated in certain specific samples. The chemical compositions are highly variable over both centimeter-scale distances and between the widely separated exposures, but they clearly reflect the elemental signatures of nearby rocks. The quantity of typical basaltic soil mixed into the light-toned materials prior to excavation by the rover wheels is minimal, suggesting negligible reworking of the deposits after their initial formation. The mineralogy, geochemistry, variability, association with local compositions, and geologic setting of the deposits suggest that Paso Robles class soils likely formed as hydrothermal and fumarolic condensates derived from magma degassing and/or oxidative alteration of crustal iron sulfide deposits. Their occurrence as unconsolidated, near-surface soils permits, though does not require, an age that is significantly younger than that of the surrounding rocks.