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Ureilites are among the most common achondrites and are widely believed to sample the mantle of a single, now-disrupted, C-rich body. We analyzed 17 ureilite samples, mostly Antarctic finds, and determined their incompatible trace element abundances. In order to remove or reduce the terrestrial contamination, which is marked among Antarctic ureilites by light-REE enrichment, we leached the powdered samples with nitric acid. The residues display consistent abundances, which strongly resemble those of the pristine rocks. All the analyzed samples display light-REE depletions, negative Eu anomalies, low (Sr/Eu ∗ ) n , and (Zr/Eu ∗ ) n ratios which are correlated. Two groups of ureilites (groups A and B) are defined. Compared to group A, group B ureilites, which are the less numerous, tend to be richer in heavy REEs, more light-REE depleted, and display among the deepest Eu anomalies. In addition, olivine cores in group B ureilites tend to be more forsteritic (Mg# = 81.9–95.2) than in group A ureilites (Mg# = 74.7–86.1). Incompatible trace element systematics supports the view that ureilites are mantle restites. REE modeling suggests that their precursors were rather REE-rich (ca. 1.8–2 × CI) and contained a phosphate phase, possibly merrillite. The REE abundances in ureilites can be explained if at least two distinct types of magmas were removed successively from their precursors: aluminous and alkali-rich melts as exemplified by the Almahata Sitta trachyandesite (ALM-A), and Al and alkali-poor melts produced after the exhaustion of plagioclase from the source. Partial melting was near fractional (group B ureilites, which are probably among the least residual samples) to dynamic with melt porosities that did not exceed a couple of percent (group A ureilites). The ureilite parent body (UPB) was almost certainly covered by a crust formed chiefly from the extrusion products of the aluminous and alkali-rich magmas. It is currently uncertain whether the Al and alkali-poor melts produced during the second phase of melting reached the surface of the body. The fact that initial silicate melting of ureilitic precursors would have produced relatively low density liquids capable of forming an external crust to the UPB casts doubt on models that invoke chondritic outer layers to achondritic asteroids. [ABSTRACT FROM AUTHOR]

Northwest Africa (NWA) 3164 and 5167 are two angrites with a granulitic texture unlike that of other angrites, with a variable, up to millimeter grain size. Besides mineralogical and chemical similarities to other angrites, NWA 3164 and 5167 exhibit unique characteristics. Ca-rich olivine dominates (in NWA 3164: ∼49 vol%, Fo 57 ; NWA 5167: 40 vol%, Fo 59 ). Fassaitic clinopyroxene is the second major phase (in NWA 3164: 29 vol%; in NWA 5167: 36 vol%) with a significant Tschermak component. In addition, two Al-rich phases are present: plagioclase An 99 and hercynitic spinel (∼6 and ∼7 vol% respectively for NWA 3164; 17 and 4 vol% respectively for NWA 5167). Heavily weathered iron sulfide and kamacite, (9 wt% in NWA 3164; 4 wt% in NWA 5167) are the remaining minor phases, a unique feature among angrites. All mineral phases are homogeneous. Like other angrites, NWA 3164 and 5167 exhibit a superchondritic Ca/Al ratio, with negligible amounts of alkalis and very low silica content. The presence of metal results from the incorporation of exogenous iron following impact. Subsequent annealing resulted in the observed granulitic texture. Major element composition indicates that both NWA 3164 and 5167 are derived from a picritic angrite precursor after incorporation of metal and annealing. After correction for iron and Fo 90 olivine incorporation, bulk rock REE abundances of both NWA 3164 and NWA 5167 appear lower than those of quenched angrites, showing the lowest absolute abundances among angrites. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analyses of clinopyroxene, olivine and anorthite indicate that difference of Rare Earth Element (REE) abundances between NWA 3164 and NWA 5167 can be explained by adding traces of phosphate to NWA 3164. NWA 3164/5167 trace elements abundances are similar, showing depletion in volatile elements and enrichment in refractory lithophile elements such as Ca, Ti, and Al. The most incompatible elements are depleted as well, unlike other angrites. This indicates that the source of these younger angrites was more depleted in incompatible elements when compared to the older magmatic angrites. The low Hf/W is understood as the result of exogenous iron incorporation and therefore the Hf/W and W isotopic heterogeneity of the angrite parent body (APB) mantle is secondary. Comparison with other angrites suggests that iron incorporation may be necessary to explain their low Hf/W and W isotopic compositions. [ABSTRACT FROM AUTHOR]

Presents research which investigated the solubility data of argon in olivine melt at very high pressure. Importance of the solubility of rare gases in silicate melts and minerals at high pressures; Role of rare gases, especially argon (Ar) in the Earth's mantle structure; Use of geochemical models; Argon solubility strongly dependent on pressure.