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The link between the Milton pallasite and the South Byron Trio irons is examined through metallography and metallogaphic cooling rates; major, minor, and trace element compositions of metal; inclusion mineralogy and mineral compositions; and oxygen isotopic compositions. The metallic hosts of these Ni-rich meteorites (18.2–20.3 wt% Ni) are dominated by plessite with spindles of kamacite and schreibersite. The presence of ∼50 nm wide tetrataenite and absence of high-Ni particles in the cloudy zone in Milton suggest cooling of ∼2000 K/Myr or >10,000 K/Myr. Compositionally, the metallic host in all four meteorites exhibits modest (1–2 orders of magnitude compared to CI chondrites) depletions of volatile elements relative to refractory elements, and marked depletions in the redox sensitive elements W, Mo, Fe, and P. Oxygen isotopic compositions (Δ17O) are, within uncertainty, the same for the Milton and the South Byron Trio and for IVB irons. Similarities in metallography, metal composition, inclusion mineralogy, and oxygen (Δ17O), molybdenum and ruthenium isotopic composition suggest that the Milton pallasite and South Byron Trio irons could have originated on a common parent body as chemically distinct melt, or on separate parent bodies that experience similar cosmochemical and geochemical processes. The Milton pallasite and South Byron Trio irons share a number of properties with IVB irons, including metallography, enrichment in highly siderophile elements and nickel, inclusion mineralogy and oxygen isotopic composition, suggesting they formed in a similar nebular region through common processes, although Milton and the South Byron Trio did not experience the dramatic volatile loss of the IVB irons. Depletions in W, Mo, Fe, and P relative to elements of similar volatility likely result from oxidation, either in the nebula prior to accretion or on the parent body during melting. Oxidation of ∼73 wt% Fe is indicated, with a correspondingly FeO-rich mantle and smaller core. If Milton and the South Byron Trio sample a common core, Milton formed near the surface of the core after stripping of the silicate shell and may have experienced rapid solidification and contamination by an impactor. The molten core, from which the South Byron Trio irons crystallized, solidified from the outside in.

The petrogenesis of the ungrouped iron meteorite Lewis Cliffs (LEW) 86211 and its proposed pair LEW 86498 has remained elusive in the decades since their discovery in Antarctica. Wasson (1990) and Kracher et al. (1998) noted the enrichment in the siderophile refractory elements, fine-grained texture, and high abundances of sulfides in LEW 86211 as features that are both difficult to explain and that set it apart from other iron meteorites. In this work, we investigate the pairing and formation of these two ungrouped iron meteorites using a combination of petrography, electron microprobe analyses, and secondary ion probe analyses of oxygen-three isotope of olivine. Similarities in petrographic features and phase compositions further support the initial pairing of LEW 86211 and 86498. The bulk composition of LEW 86211 (Wasson, 1990) closely resembles those of separated chondritic metallic components (e.g., Kong and Ebihara, 1997), which indicates this pairing group formed directly from this portion of a chondrite. The metal-sulfide cellular textures and mineral compositional trends are consistent with LEW 86211 and 86498 forming by rapid cooling of the FeNiS immiscible liquid of a larger chondritic impact melt unit. Previous bulk oxygen-three isotope analyses (Clayton and Mayeda, 1996) combined with the in situ oxygen-three isotope analyses from this work are consistent with LEW 86211 having a carbonaceous chondrite provenance. LEW 86211 is most similar to CR chondrites in its oxygen-three isotope signatures, but may not be from an established carbonaceous chondrite group. The silicate inclusions in LEW 86211 and 86498 record evidence of pre-impact metamorphism and later reduction related to contact with the metal-sulfide impact melt liquid. The silicate inclusions appear to have been engulfed by metal-sulfide liquids rather than part of the impact melted unit. Additionally, the size of this sulfide-dominated pairing group compared to the volume of sulfides and metal in unmelted CR chondrite suggests that these meteorites originated from a much larger carbonaceous chondrite impact melt body than has been previously recognized (e.g., Lunning et al., 2016).

The Psyche mission’s Oxidation-Reduction Working Group is focused on understanding, determining, and applying the redox state of (16) Psyche to understand the origin of a metal-rich world. The oxidation-reduction state of an asteroid, along with its temperature, parent body size, and composition, is a key parameter in determining the history of an asteroid. Determining the redox state from spacecraft data is most easily done by examining potential metal-oxide buffer pairs. The occurrence of Ni, Fe, C, Cr, P and Si, in that order, in the metal or sulfide phase of an asteroidal body indicates increasingly reduced conditions. Key observations by the Imager and Gamma-Ray and Neutron Spectrometer (GRNS) of Psyche can bracket the redox state using metal-oxide buffers. The presence of Fe,Ni metal can be confirmed by the ratios of Fe/O or Fe/Si and the concentration of Ni variability in metal across the asteroid can be determined by GRNS. The FeO concentration of silicates is complementary to the Ni concentration of metal and can be constrained using filters on the Imager. The presence of FeO in silicates from ground-based observations is one of the few measurements we already have of redox state, although available data permit a wide range of silicate compositions and mineralogies. The presence of C, P or Si concentrated in the metallic, Fe-rich portion of the asteroid, as measured by GRNS, or Ca-sulfide, determined by imaging, would indicate increasingly reducing conditions. Linkage to known types of meteorites, whether metal-rich chondrites, stony-irons or irons, expands the mineralogical, chemical and isotopic data not available from remote observations alone. Redox also controls both silicate and metal mineralogy, influencing differentiation, solidification, and subsolidus cooling, including the relative abundance of sulfur in the core and possible magnetic signatures. The redox state of Psyche, if a fully-differentiated metallic core, might constrain the location and timing of both the formation of Psyche and any oxidation it might have experienced.

The Hamburg meteorite fell on January 16, 2018, near Hamburg, Michigan, after a fireball event widely observed in the U.S. Midwest and in Ontario, Canada. Several fragments fell onto frozen surfaces of lakes and, thanks to weather radar data, were recovered days after the fall. The studied rock fragments show no or little signs of terrestrial weathering. Here, we present the initial results from an international consortium study to describe the fall, characterize the meteorite, and probe the collision history of Hamburg. About 1kg of recovered meteorites was initially reported. Petrology, mineral chemistry, trace element and organic chemistry, and O and Cr isotopic compositions are characteristic of H4 chondrites. Cosmic ray exposure ages based on cosmogenic 3He, 21Ne, and 38Ar are ~12Ma, and roughly agree with each other. Noble gas data as well as the cosmogenic 10Be concentration point to a small 40-60cm diameter meteoroid. An 40Ar-39Ar age of 4532±24Ma indicates no major impact event occurring later in its evolutionary history, consistent with data of other H4 chondrites. Microanalyses of phosphates with LA-ICPMS give an average Pb-Pb age of 4549±36Ma. This is in good agreement with the average SIMS Pb-Pb phosphate age of 4535.3±9.5Ma and U-Pb Concordia age of 4535±10Ma. The weighted average age of 4541.6±9.5Ma reflects the metamorphic phosphate crystallization age after parent body formation in the early solar system.

We investigated the metal‐rich chondrite Sierra Gorda (SG) 009, a member of the new G chondrite grouplet (also including NWA 5492, GRO 95551). G chondrites contain 23% metal, very reduced silicates, and rare oxidized mineral phases (Mg‐chromite, FeO‐rich pyroxene). G chondrites are not related to CH‐CB chondrites, based on bulk O, C, and N isotopic compositions, mineralogy, and geochemistry. G chondrites have no fine‐grained matrix or matrix lumps enclosing hydrated material typical for CH‐CB chondrites. G chondrites’ average metal compositions are similar to H chondrites. Siderophile and lithophile geochemistry indicates sulfidization and fractionation of the SG 009 metal and silicates, unlike NWA 5492 and GRO 95551. The G chondrites have average O isotopic compositions Δ17O>0‰ ranging between bulk enstatite (E) and ordinary (O) chondrites. An Al‐rich chondrule from SG 009 has Δ17O>0‰ indicating some heterogeneity in oxygen isotopic composition of G chondrite components. SG 009’s bulk carbon and nitrogen isotopic compositions correspond to E and O chondrites. Neon isotopic composition reflects a mixture of cosmogenic and solar components, and cosmic ray exposure age of SG 009 is typical for O, E, and R chondrites. G chondrites are closely related to O, E, and R chondrites and may represent a unique metal‐rich parent asteroid containing primitive and fractionated material from the inner solar system. Oxidizing and reducing conditions during SG 009 formation may be connected with a chemical microenvironment and possibly could indicate that G chondrites may have formed by a planetesimal collision resulting in the lack of matrix.

The meteorites Graves Nunataks (GRA) 06128 and 06129 are igneous meteorites dominated by oligoclase feldspar and have basaltic trachyandesite-like whole rock compositions. Formation of the GRA 06128/9 meteorites as primary melts on an oxidized planetesimal has been previously proposed (Day et al. 2009a, 2012a; Gardner-Vandy et al., 2013; Wang et al., 2014). We show experimentally that anhydrous partial melting of an oxidized R chondrite at IW to IW+1 between 1120–1140 °C produces melts of GRA 06128/9-like compositions: intermediate SiO 2 and FeO concentrations that are enriched in volatile sodium. From a process perspective, GRA 06128/9-like magmas are complementary to partial melt residues such as olivine-rich brachinite and FeO-rich brachinite-like meteorites. Magmas of GRA 06128/9’s composition can be generated under equilibrium conditions, as demonstrated by MELTS modeling, but only at temperatures ∼1140 °C. At lower degrees of partial melting liquids formed under equilibrium and non-equilibrium conditions follow distinct compositional pathways to reach GRA 06128/9-like melts. For lower degrees of melting, the non-equilibrium trend more closely resembles GRA 06128/9’s composition. Phase abundance modeling indicates that GRA 06128/9-composition magmas form by 14–22% silicate melting of an oxidized R-chondrite. We conclude that GRA 06128/9-composition magmas can be generated at ∼1140 °C from partial melting of an oxidized chondritic precursor under both non-equilibrium and equilibrium conditions.

204 howardites in the National Meteorite Collection at the Smithsonian were examined for the presence of fine-grained eucrite clasts, with the goal of better understanding the formation of the uppermost crust of asteroid 4Vesta. Eight clasts were identified and characterized in terms of their textures and mineral chemistry, and their degree of thermal metamorphism was assessed. The paucity of fine-grained eucrites, both within the unbrecciated eucrites and as clasts within the howardites, suggests that they originate from small-scale units on the surface of Vesta, most likely derived from partial melting. Six of the eight clasts described were found to be unequilibrated, meaning that they preserve their original crystallization trends. The vast majority of eucrites are at least partially equilibrated, making these samples quite rare and important for deciphering the petrogenesis of the vestan crust. Biomodal grain populations suggest that eucrite melts often began crystallizing pyroxene and plagioclase during their ascent to the surface, where they were subject to more rapid cooling, crystallization, and later metasomatism. Pyroxene compositions from this study and prior work indicate that the products of both primitive and evolved melts were present at the vestan surface after its formation. Two howardite thin sections contained multiple eucrite composition clasts with different crystallization and thermal histories; this mm-scale diversity reflects the complexity of the current day vestan surface that has been observed by Dawn.

Volatile-rich and typically oxidized carbonaceous chondrites, such as CV and CM chondrites, potentially respond to impacts differently than do other chondritic materials. Understanding impact melting of carbonaceous chondrites has been hampered by the dearth of recognized impact melt samples. In this study we identify five carbonaceous chondrite impact melt clasts in three host meteorites: a CV3red chondrite, a CV3oxA chondrite, and a regolithic howardite. The impact melt clasts in these meteorites respectively formed from CV3red chondrite, CV3oxA chondrite, and CM chondrite protoliths. We identified these impact melt clasts and interpreted their precursors based on their texture, mineral chemistry, silicate bulk elemental composition, and in the case of the CM chondrite impact melt clast, in situ measurement of oxygen three-isotope signatures in olivine. These impact melts typically contain euhedral–subhedral olivine microphenocrysts, sometimes with relict cores, in glassy groundmasses. Based on petrography and Raman spectroscopy, four of the impact melt clasts exhibit evidence for volatile loss: these melt clasts either contain vesicles or are depleted in H2O relative to their precursors. Volatile loss (i.e., H2O) may have reduced the redox state of the CM chondrite impact melt clast. The clasts that formed from the more oxidized precursors (CV3oxA and CM chondrites) exhibit phase and bulk silicate elemental compositions consistent with higher intrinsic oxygen fugacities relative to the clast that formed from a more reduced precursor (CV3red chondrite). The mineral chemistries and assemblages of the CV and CM chondrite impact melt clasts identified here provide a template for recognizing carbonaceous chondrite impact melts on the surfaces of asteroids.

Although acapulcoites and lodranites played a key role in understanding partial differentiation of asteroids, the lack of samples of the chondritic precursor limits our understanding of the processes that formed these meteorites. Grove Mountains (GRV) 020043 is a type 4 chondrite, with abundant, well-delineated, pyroxene-rich chondrules with an average diameter of 690 μm, microcrystalline mesostasis, polysynthetically striated low-Ca pyroxene, and slightly heterogeneous plagioclase compositions. Similarities in mineralogy, mineral composition, and oxygen isotopic composition link GRV 020043 to the acapulcoite-lodranite clan. These features include a high low-Ca pyroxene to olivine ratio, high kamacite to taenite ratio, and relatively FeO-poor mafic silicates (Fa10.3, Fs10.4) relative to ordinary chondrites, as well as the presence of ubiquitous metal and sulfide inclusions in low-Ca pyroxene and ƒO2 typical of acapulcoites. GRV 020043 shows that evidence of partial melting is not an essential feature for classification within the acapulcoite-lodranite clan. GRV 020043 experienced modest thermal metamorphism similar to type 4 ordinary chondrites. GRV 020043 suggests a range of peak temperatures on the acapulcoite-lodranite parent body similar to that of ordinary chondrites, but shifted to higher temperatures, perhaps consistent with earlier accretion. The mineralogy and mineral compositions of GRV 020043, despite modest thermal metamorphism, suggests that most features of acapulcoites previously attributed to reduction were, instead, inherited from the precursor chondrite. Although partial melting was widespread on the acapulcoite-lodranite parent body, ubiquitous Fe,Ni-FeS blebs in the cores of silicates were not implanted by shock or trapped during silicate melting, but were inherited from the precursor chondrite with subsequent overgrowths during metamorphism.

Nakhlites, clinopyroxenite meteorites from Mars, share common crystallization and ejection ages, suggesting that they might have been ejected from the same place on Mars by the same ejection event (impact) and are different samples of the same thick volcanic flow unit or shallow sill. Mean modal abundances and abundance ranges of pyroxene, olivine, and mesostasis vary widely among different thin-sections of an individual nakhlite. Lithologic heterogeneity is the main factor contributing to the observed modal-abundance variations measured in thin-sections prepared from different fragments of the same stone. Two groups of nakhlites are distinguished from one another by which major constituent varies the least and the abundance of that constituent. The group consisting of Nakhla, Lafayette, Governador Valadares, and the Yamato nakhlite pairing group is characterized by low modal mesostasis and pyroxene-olivine covariance, whereas the group consisting of the Miller Range nakhlite pairing group and Northwest Africa 5790 is characterized by low modal olivine and pyroxene-mesostasis covariance. These two groups sample the slowest-cooled interior portion and the chilled margin, respectively, of the nakhlite emplacement body as presently understood, and appear to be also related to recently proposed nakhlite groups independently established using compositional rather than petrographic observations. Phenocryst modal abundances vary with inferred depth in the nakhlite igneous body in a manner consistent with solidification of the nakhlite stack from dynamically sorted phenocryst-rich magmatic crystal-liquid mush.

Significance Martian meteorite ALH 84001 serves as a witness plate to the history of the Martian climate ∼4 Ga ago. This study describes ion microprobe δ 18 O analyses coupled with δ 13 C, δ 18 O, and Δ 17 O analyses from stepped acid dissolution of the meteorite that identifies a new carbonate phase with distinct isotope compositions. These new measurements of the oxygen isotope composition of carbonates within this meteorite reveal several episodes of aqueous activity that were strongly influenced by atmospheric chemistry. When paired with carbon isotope measurements, these data suggest that the ancient atmosphere of Mars was significantly depleted in 13 C compared to the present day. This implies substantial enrichment in the δ 13 C of the atmosphere since the Noachian which may have occurred through extensive atmospheric loss.

This article will discuss the unique way in which nursing education at one Catholic University is distinctively value-driven with a focus on the meaning of Mercy and Jesuit traditions and how these philosophies translate into professional nursing practice. An innovative approach to a value-driven education that incorporates the philosophy of the Mercy and Jesuit traditions in a professional nursing role is fostered with the teachings of Catherine McAuley and Ignatius Loyola and infused through the act of service-learning and reflection on the service-learning experience. Nursing students are educated from a perspective of historical tradition, spirituality, social justice, reflective thinking and a value-centered professional education, enriching their self-awareness toward the development of leadership behaviors. Linking the service-learning experience to nursing concepts within the Mercy and Jesuit traditions has demonstrated a deep sense of self-awareness, a high level of understanding of caring and the concept of nurses as leaders amongst the students at our university.

Identifying and mapping olivine on asteroid 4 Vesta are important components to understanding differentiation on that body, which is one of the objectives of the Dawn mission. Harzburgitic diogenites are the main olivine-bearing lithology in the howardite-eucrite-diogenite (HED) meteorites, a group of samples thought to originate from Vesta. Here, we examine all the Antarctic harzburgites and estimate that, on scales resolvable by Dawn, olivine abundances in putative harzburgite exposures on the surface of Vesta are likely at best in the 10–30% range, but probably lower due to impact mixing. We examine the visible/near-infrared spectra of two harzburgitic diogenites representative of the 10–30% olivine range and demonstrate that they are spectrally indistinguishable from orthopyroxenitic diogenites, the dominant diogenitic lithology in the HED group. This suggests that the visible/near-infrared spectrometer onboard Dawn (VIR) will be unable to resolve harzburgites from orthopyroxenites on the surface of Vesta, which may explain the current lack of identification of harzburgitic diogenite on Vesta.

The Institute of Medicine and the American Association of Colleges of Nursing advise that professional nursing education include development of a high level of cultural competency. A 10-day learning experience to Ireland for nursing students at the University of Detroit Mercy, an independent Catholic university, sponsored by the Sisters of Mercy and the Society of Jesus (Jesuit Fathers), helped them develop a philosophy of Mercy care and build cultural competence. Learning focused on the life of Catherine McAuley, Irish culture, spirituality, social justice, reflective thinking, and a value-centered professional education.

A laser ablation mass spectrometer (LAMS) based on a time-of-flight (TOF) analyzer with adjustable drift length is proposed as a standoff elemental composition sensor for space missions to airless bodies. It is found that the use of a retarding potential analyzer in combination with a two-stage reflectron enables LAMS to be operated at variable drift length. For field-free drift lengths between 33 cm to 100 cm, at least unit mass resolution can be maintained solely by adjustment of internal voltages, and without resorting to drastic reductions in sensitivity. Therefore, LAMS should be able to be mounted on a robotic arm and analyze samples at standoff distances of up to several tens of cm, permitting high operational flexibility and wide area coverage of heterogeneous regolith on airless bodies.

– The Old Woman meteorite, discovered in March 1976 by two prospectors searching for a fabled lost Spanish gold mine in mountains ∼270 km east of Los Angeles, has achieved the status of a legend among meteorite hunters and collectors. The question of the ownership of the 2753 kg group IIAB meteorite, the second largest ever found in the United States (34°28′N, 115°14′W), gave rise to disputes involving the finders, the Bureau of Land Management, the Secretary of the Department of the Interior, the State of California, the California members of the U.S. Congress, various museums in California, the Smithsonian Institution, and the Department of Justice. Ultimately, ownership of the meteorite was transferred to the Smithsonian under the powers of the 1906 Antiquities Act, a ruling upheld in a U.S. District Court and a U.S. Court of Appeals. After additional debate, the Smithsonian removed a large cut for study and curation, and for disbursement of specimens to qualified researchers. The main mass was then returned to California on long-term loan to the Bureau of Land Management’s Desert Discovery Center in Barstow. The Old Woman meteorite litigation served as an important test case for the ownership and control of meteorites found on federal lands. The Old Woman meteorite appears to be structurally unique in containing both hexahedral and coarsest octahedral structures in the same mass, unique oriented schreibersites within hexahedral areas, and polycrystalline parent austenite crystals. These structures suggest that different portions of the meteorite may have transformed via different mechanisms upon subsolidus cooling, making the large slices of Old Woman promising targets for future research.

We report analyses of 14 group IVA iron meteorites, and the ungrouped but possibly related, Elephant Moraine (EET) 83230, for siderophile elements by laser ablation ICP-MS and isotope dilution. EET was also analyzed for oxygen isotopic composition and metallographic structure, and Fuzzy Creek, currently the IVA with the highest Ni concentration, was analyzed for metallographic structure. Highly siderophile elements (HSE) Re, Os and Ir concentrations vary by nearly three orders of magnitude over the entire range of IVA irons, while Ru, Pt and Pd vary by less than factors of five. Chondrite normalized abundances of HSE form nested patterns consistent with progressive crystal–liquid fractionation. Attempts to collectively model the HSE abundances resulting from fractional crystallization achieved best results for 3 wt.% S, compared to 0.5 or 9 wt.% S. Consistent with prior studies, concentrations of HSE and other refractory siderophile elements estimated for the bulk IVA core and its parent body are in generally chondritic proportions. Projected abundances of Pd and Au, relative to more refractory HSE, are slightly elevated and modestly differ from L/LL chondrites, which some have linked with group IVA, based on oxygen isotope similarities. Abundance trends for the moderately volatile and siderophile element Ga cannot be adequately modeled for any S concentration, the cause of which remains enigmatic. Further, concentrations of some moderately volatile and siderophile elements indicate marked, progressive depletions in the IVA system. However, if the IVA core began crystallization with � 3 wt.% S, depletions of more volatile elements cannot be explained as a result of prior volatilization/condensation processes. The initial IVA core had an approximately chondritic Ni/Co ratio, but a fractionated Fe/Ni ratio of � 10, indicates an Fedepleted core. This composition is most easily accounted for by assuming that the surrounding silicate shell was enriched in iron, consistent with an oxidized parent body. The depletions in Ga may reflect decreased siderophilic behavior in a relatively oxidized body, and more favorable partitioning into the silicate portion of the parent body. Phosphate inclusions in EET show D 17 O values within the range measured for silicates in IVA iron meteorites. EET has a typical ataxitic microstructure with precipitates of kamacite within a matrix of plessite. Chemical and isotopic evidence for a genetic relation between EET and group IVA is strong, but the high Ni content and the newly determined, rapid cooling rate of this meteorite show that it should continue to be classified as ungrouped. Previously reported metallographic cooling rates for IVA iron meteorites have been interpreted to indicate an inwardly crystallizing, � 150 km radius metallic body with little

Laboratory studies of meteorites and robotic exploration of Mars reveal scant atmosphere, no evidence of plate tectonics, past evidence for abundant water, and a protracted igneous evolution. Despite indirect hints, direct evidence of a martian origin came with the discovery of trapped atmospheric gases in one meteorite. Since then, the study of martian meteorites and findings from missions have been linked. Although the meteorite source locations are unknown, impact ejection modeling and spectral mapping of Mars suggest derivation from small craters in terrains of Amazonian to Hesperian age. Whereas most martian meteorites are young ( 4.5 Ga and formation of enriched and depleted reservoirs. However, the history inferred from martian meteorites conflicts with results from recent Mars missions, calling into doubt whether the igneous histor y inferred from the meteorites is applicable to Mars as a whole. Allan Hills 84001 dates to 4.09 Ga and contains fluid-deposited carbonates. Accompanying debate about the mechanism and temperature of origin of the carbonates came several features suggestive of past microbial life in the carbonates. Although highly disputed, the suggestion spurred interest in habitable extreme environments on Earth and throughout the Solar System. A flotilla of subsequent spacecraft has redefined Mars from a volcanic planet to a hydrologically active planet that may have harbored life. Understanding the history and habitability of Mars depends on understanding the coupling of the atmosphere, surface, and subsurface. Sample return that brings back direct evidence from these diverse reservoirs is essential.

We investigate the relationship between the petrology and visible-near infrared spectra of the unbrecciated eucrites and synthetic pyroxene-plagioclase mixtures to determine how spectra obtained by the Dawn mission could distinguish between several models that have been suggested for the petrogenesis of Vesta's crust (e.g., partial melting and magma ocean). Here, we study the spectra of petrologically characterized unbrecciated eucrites to establish spectral observables, which can be used to yield mineral abundances and compositions consistent with petrologic observations. No information about plagioclase could be extracted from the eucrite spectra. In contrast, pyroxene dominates the spectra of the eucrites and absorption band modeling provides a good estimate of the relative proportions of low- and high-Ca pyroxene present. Cr is a compatible element in eucrite pyroxene and is enriched in samples from primitive melts. An absorption at 0.6 lm resulting from Cr 3+ in the pyroxene structure can be used to distinguish these primitive eucrites. The spectral differences present among the eucrites may allow Dawn to distinguish between the two main competing models proposed for the petrogenesis of Vesta (magma ocean and partial melting). These models predict different crustal structures and scales of heterogeneity, which can be observed spectrally. The formation of eucrite Allan Hills (ALH) A81001, which is primitive (Cr-rich) and relatively unmetamorphosed, is hard to explain in the magma ocean model. It could only have been formed as a quench crust. If the magma ocean model is correct, then ALHA81001-like material should be abundant on the surface of Vesta and the Vestoids.

To better understand the partitioning behavior of elements during the formation and evolution of iron meteorites, two sets of experiments were conducted at 1 atm in the Fe–Ni–P system. The first set examined the effect of P on solid metal/liquid metal partitioning behavior of 22 elements, while the other set explored the effect of the crystal structures of body-centered cubic (α)- and face-centered cubic (γ)-solid Fe alloys on partitioning behavior. Overall, the effect of P on the partition coefficients for the majority of the elements was minimal. As, Au, Ga, Ge, Ir, Os, Pt, Re, and Sb showed slightly increasing partition coefficients with increasing P-content of the metallic liquid. Co, Cu, Pd, and Sn showed constant partition coefficients. Rh, Ru, W, and Mo showed phosphorophile (P-loving) tendencies. Parameterization models were applied to solid metal/liquid metal results for 12 elements. As, Au, Pt, and Re failed to match previous parameterization models, requiring the determination of separate parameters for the Fe–Ni–S and Fe–Ni–P systems. Experiments with coexisting α and γ Fe alloy solids produced partitioning ratios close to unity, indicating that an α versus γ Fe alloy crystal structure has only a minor influence on the partitioning behaviors of the trace element studied. A simple relationship between an element’s natural crystal structure and its α/γ partitioning ratio was not observed. If an iron meteorite crystallizes from a single metallic liquid that contains both S and P, the effect of P on the distribution of elements between the crystallizing solids and the residual liquid will be minor in comparison to the effect of S. This indicates that to a first order, fractional crystallization models of the Fe–Ni–S–P system that do not take into account P are appropriate for interpreting the evolution of iron meteorites if the effects of S are appropriately included in the effort.