Ureilite Parent Body Research Articles

Extra-terrestrial mantle samples: Rare Earth Element variations and evidence for melt metasomatism in ureilite meteorites

Ureilites are meteorites derived from the mantle of a reduced differentiated asteroid, the “Ureilite Parent Body” (UPB), which was later disrupted by impact with another Solar System body. They have ultramafic compositions dominated mostly by olivine and pigeonite with rare orthopyroxene and augite; aluminous phases are generally absent. Ureilites vary from abundant peridotites to much rarer pyroxenites, and their core olivine compositions range from Fo74 to Fo97 across different samples. The UPB experienced sufficiently high temperatures to undergo silicate partial melting, as shown by depletion in the Light Rare Earth Elements (LREE) in bulk restitic ureilites. Plagioclase and merrillite were probably present in the UPB mantle but have been completely removed during silicate partial melting. Partial melts of the UPB mantle are represented by glassy melt inclusions, igneous clasts in ureilite breccias, cumulus augite in some ureilites, and rare trachyandesitic fragments. These melts are generally intermediate and sub-alkaline in composition, although a few are alkaline. They have more enriched and flatter bulk REE patterns than the restitic ureilites and often show positive Eu anomalies. Glasses (representing melts) in ureilites from this study range from 57 to 79 wt% SiO2. One sample (AhS 22) shows petrographic and geochemical evidence for interaction between magma and the solid UPB mantle by forming metasomatic augite.Silicate minerals in ureilites analysed by LA-ICP-MS are generally LREE-depleted, with negative Eu anomalies. Ureilitic olivines have the lowest REE contents and the smallest negative Eu anomalies. Low-Ca pyroxenes have similar patterns with slightly stronger Eu anomalies. Augites have the highest REE contents and the most negative Eu anomalies. Augites show REE disequilibrium with olivine and low-Ca pyroxene, suggesting that they were not part of the restitic assemblage but were added by silicate melts passing through the UPB mantle, i.e. they are metasomatic in origin. We also discuss the size of the original UPB, using silicate minerals as evidence for it being a typical asteroid rather than a planet-sized object.

53Mn-53Cr chronometry of ureilites: Implications for the timing of parent body accretion, differentiation and secondary reduction

Establishing the temporal evolution of the ureilite parent body(ies) is crucial for understanding the quantitative timescale of planetesimal formation and evolution in the protoplanetary disk. In order to establish a timeline for these early processes, age constraints on the accretion, differentiation and secondary reduction were obtained with the short-lived 53Mn-53Cr chronometer to whole-rock and sequentially digested fractions of main group ureilites. A whole-rock isochron dates the reservoir-scale Mn-Cr fractionation in the ureilite parent body(ies), associated with magmatic differentiation, to 2.89-0.51+0.56 Ma after CAI formation. This age implies that the ureilite parent body(ies) accreted no later than ∼1.5 Ma after CAI formation, at a time when the NC-CC dichotomy was already established. The 53Mn-53Cr systematics of fractions from chromite-bearing ureilites yield an age of 4.29-0.45+0.49 Ma after CAI formation for a secondary reduction event on the parent body. This event is commonly associated with the catastrophic disruption of the ureilite parent body while still hot. The chromite model ages are consistent with the isochron ages obtained from chromite-bearing ureilites. Collectively these ages indicate that chemical differentiation processes were underway on the ureilite parent body(ies) during the time interval when undifferentiated meteorite parent bodies were forming, and may have paused at the peak of planetesimal formation when planetary collisions were common.

NWA 11562: A Unique Ureilite with Extreme Mg-rich Constituents

A comprehensive study of an ungrouped achondrite meteorite, North West Africa (NWA) 11562, was conducted, involving petrology, mineralogy, and mass-independent chromium isotopic composition. NWA 11562 comprises 34.9 vol% olivine, 56.1 vol% pyroxenes, 6.7 vol% Fe–Ni metal and oxides, 2.2 vol% carbon, and 0.2 vol% anhydrite. The oxygen isotopic composition (δ 18O = 6.24‰ ± 0.13‰ and Δ17O = −1.81‰ ± 0.03‰; Meteoritical Bulletin Database) and chromium isotopic compositions (ε 54Cr = −0.82 ± 0.10, 2SE) are consistent with NWA 11562 being a ureilite, and petrographic observations show features similar to those of the common ureilite group meteorites. Olivine (core: Fo99.0 ± 0.1; rim: Fo98.9 ± 0.1) and pyroxene (orthopyroxene: Mg# 99.0 ± 0.2; clinopyroxene: Mg# 99.1 ± 0.7) core compositions are more magnesian than in any previously known ureilite and lack the characteristic reduction rims of ureilites. Rounded small olivine grains within NWA 11562 indicate that the meteorite experienced impact and associated melting. Combined with the characteristic Fe/Mn ratio (3.84 ± 0.16) and Mg# (99.0 ± 0.1) of olivine cores, we suggest that NWA 11562 represents a more Mg-rich ureilite than any previously reported. NWA 11562 has a high 55Mn/52Cr ratio, and when combined with literature data, it plots on a well-defined 53Mn–53Cr isochron, providing a more accurate age, i.e., 4566.7 ± 0.8 Ma, overlapping previous work. This age may represent the result of early partial melting of the ureilite parent body.

Iron isotope fractionation between metal and silicate during core-mantle differentiation in rocky bodies

Fe isotope variations in rocky bodies reveal fundamental information about planetary evolution. However, experimental results have come to contradictory conclusions on the equilibrium Fe isotope fractionation between metal and silicate during core-mantle differentiation. Many different processes, including evaporation, core formation, partial melting and disproportion of mantle silicate, have been consequently proposed to explain the observed Fe isotope variations in rocky solar system bodies. Here we perform ab initio molecular dynamics simulations and find that the anharmonicity in iron strongly decreases the force constant of Fe at low pressures (<∼50 GPa), which even reverses the equilibrium Fe isotope fractionation between metal and silicate. We conclude that pyrolitic melt is always enriched in heavy Fe isotopes relative to liquid Fe-alloys, no matter what pressure. Therefore core-mantle differentiation will play a significant role in explaining the heavy Fe isotope compositions of the mantles of some rocky bodies (e.g., Earth, the ureilite parent body, and possibly the asteroid Vesta). As all previously proposed processes for Fe isotope fractionation can only enrich the mantle-derived rocks in heavy Fe isotopes, the near/sub-chondritic Fe isotope signatures of Mars and the aubrite parent body thus imply that iron sulfide enriched in light Fe isotopes may significantly contribute to the iron components of those meteoritic samples.

The catastrophic break‐up of the ureilite parent body: Modeling constraints on the debris size

AbstractThe ureilite parent body (UPB) was, in all likelihood, completely broken apart when hit by another object early in its history and reassembled into daughter bodies. We here present a study tailored to constrain the dimensions of the impact debris produced in the catastrophic disruption. Using a customized Python code to simulate the thermal evolution of the UPB fragments, we compared the FeO profiles modeled for different depths within those fragments with those measured across the reduction rims in olivines of 12 different ureilites (n = 37). Our profile data were fitted to the theoretical cooling profiles determined with a transient thermal model. The results are coherent and consistent with earlier studies and, despite using simplified boundary conditions (fragments described as ideal spheres and maximum radiation), our data provide valuable context on possible cooling pathways of the UPB debris. In detail, we found that the average depths within the given fragments from which our samples of ureilites originated were limited to 0.3–0.4 ± 0.1 m, with only few exceptions (e.g., one highly reduced sample lacked suitable reduction profiles suggesting either a depth of origin of &gt;2 m or shielding of this fragment from rapid cooling, e.g., due to hovering in the center of a relatively dense cloud of debris). In addition, we calculated that the cooling from 1473 to 1100 K of the average fragment at the depth of our samples took no more than 3–4 days, suggesting that the reassembly of the ureilite daughter bodies could have been a very fast process.

Hydrogen in acapulcoites and lodranites: A unique source of water for planetesimals in the inner Solar System

Acapulcoites and lodranites are primitive achondrites, sampling a common planetesimal formed a few million years after calcium-aluminium rich inclusions in the inner Solar System, that provides information into melting and differentiation processes in the early inner Solar System. The chemistry and mineralogy of their chondritic parent body lies in between enstatite and ordinary chondrites. As they record a range in planetary differentiation degree, from 1% up to 20% partial melting, with lodranites experiencing the most melt extraction, we investigate (i) the behaviour of hydrogen in terms of abundance and isotopic composition during the early stages of planetary differentiation and (ii) the source(s) of hydrogen for the acapulcoite-lodranite parent body in order to place it in our current understanding of the source(s) of water in the inner Solar System. In this study, we analysed water content and hydrogen isotopic composition of phosphates and nominally anhydrous minerals in a range of acapulcoite and lodranite meteorite samples. While apatites seemed to have recorded a degassing signature, no such variations were observed in the H2O–δD systematics of the nominally anhydrous minerals suggesting that subsequent to their crystallisation, acapulcoites and lodranites experienced minimal modifications to their volatile composition during thermal metamorphism and partial melting. The low abundance of water in acapulcoite and lodranite nominally anhydrous minerals (i.e., average 5.2±1.6 μg/g H2O) suggests that their parent body was much drier than what has been estimated for enstatite and ordinary chondrite parent bodies. We estimated a bulk water content for the acapulcoite-lodranite parent body of 3 to 19 μg/g H2O, similar to the ureilite parent body. The hydrogen isotopic composition of nominally anhydrous minerals in acapulcoites and lodranites (–211±145‰), and in particular for the two falls Acapulco and Lodran (–239±149‰), matches with the hydrogen isotopic composition recorded by nominally anhydrous minerals in ordinary chondrite falls, eucrites, S–type asteroid Itokawa, consistent with a common source of water for the inner Solar System planetesimals, isotopically distinctive to bulk carbonaceous chondrites.

40Ar/39Arages ofL4,H5,EL6,and feldspathic ureilitic clasts from the Almahata Sitta polymict ureilite (asteroid 2008TC3)

AbstractThe Almahata Sitta (AhS) meteorite consists of disaggregated clasts from the impact of the polymict asteroid 2008 TC3, including ureilitic (70%–80%) and diverse non‐ureilitic materials. We determined the40Ar/39Ar release patterns for 16 AhS samples (3–1500 μg) taken from three chondritic clasts, AhS 100 (L4), AhS 25 (H5), and MS‐D (EL6), as well as a clast of ureilitic trachyandesite MS‐MU‐011, also known as ALM‐A, which is probably a sample of the crust of the ureilite parent body (UPB). Based on our analyses, best estimates of the40Ar/39Ar ages (Ma) of the chondritic clasts are 4535 ± 10 (L4), 4537–4555 with a younger age preferred (H5), and 4513 ± 17 (EL6). The ages for the L4 and the H5 clasts are older than the most published40Ar/39Ar ages for L4 and H5 meteorites, respectively. The age for the EL6 clast is typical of older EL6 chondrites. These ages indicate times of argon closure ranging up to 50 Ma after the main constituents of the host breccia, that is, the ureilitic components of AhS, reached the &gt;800°C blocking temperatures of pyroxene and olivine thermometers. We suggest that these ages record the times at which the clasts cooled to the Ar closure temperatures on their respective parent bodies. This interpretation is consistent with the recent proposal that the majority of xenolithic materials in polymict ureilites were implanted into regolith 40–60 Ma after calcium–aluminum‐rich inclusion and is consistent with the interpretation that 2008 TC3was a polymict ureilite. With allowance for its 10‐Ma uncertainty, the 4549‐Ma40Ar/39Ar age of ALM‐A is consistent with closure within a few Ma of the time recorded by its Pb/Pb age either on the UPB or as part of a rapidly cooling fragment. Plots of age versus cumulative39Ar release for 10 of 15 samples with ≥5 heating steps indicate minor losses of40Ar over the last 4.5 Ga. The other five such samples lost some40Ar at estimated times no earlier than 3800–4500 Ma bp. Clustering of ages in the low‐temperature data for these five samples suggests that an impact caused localized heating of the AhS progenitor ~2.7 Ga ago. In agreement with the published work, 10 estimates of cosmic‐ray exposure ages based on38Ar concentrations average 17 ± 5 Ma but may include some early irradiation.

The H2O content of the ureilite parent body

The fate of highly volatile elements (H, C, F, Cl and S) during planetary accretion and differentiation is debated. Recent analyses of water in non-carbonaceous chondrites (RC, OC, EC) and achondrites (angrites, eucrites) have been used to argue that inner solar system parent bodies accreted and retained their highly volatile element budgets from their primary feedstock without substantial loss during accretion, metamorphism and differentiation. An alternative model posits that differentiated inner solar system parent bodies (e.g., the angrite parent body, 4 Vesta, Earth) derived the majority of their water from a carbonaceous chondrite-like source, delivered during the final stages of accretion.In order to add new constraints to this debate, we have measured water in nominally anhydrous minerals, melt inclusions, and interstitial glass in ureilites, the largest group of primitive achondrites in the terrestrial meteorite collection. Primitive achondrites did not experience global melting and homogenization. Therefore, these meteorites capture part of the transition from chondritic to achondritic parent bodies, allowing us to constrain the fate of water during the earliest stages of differentiation. Our nano-scale secondary ion mass spectrometry (nanoSIMS) analyses allow us to assess the viability of ureilite-like material as a potential source of terrestrial water. Analyses of pigeonite in main group ureilites yield a range of 2.0 – 6.0 µg/g H2O, and analyses of high-Ca pyroxene and glass (glassy melt inclusions and interstitial glass) in the Almahata Sitta ureilitic trachyandesite yield ranges of 13 – 19 µg/g H2O and 44 – 216 µg/g H2O, respectively. Mass balance, incremental melting, and batch melting calculations yield a preferred ureilite parent body H2O content of 2 – 20 µg/g, similar to previous estimates of water in the eucrite parent body (4 Vesta), but lower than estimates of Earth’s water budget. With these data, we demonstrate that 1) the ureilite parent body is H2O-depleted relative to the Earth; 2) ureilite-like material is unlikely to be a primary source of H2O to the Earth; 3) C and H are not necessarily coupled elements during planetary accretion and thermal processing; and 4) accretion, heating, partial melting, and degassing of rocky planetesimals likely results in significant depletion of H2O.

Shock degree and graphite geothermometry in ureilites NWA 6871 and NWA 3140

AbstractCarbon aggregates from two differently shocked ureilites were analyzed to gain insight into the shock transformation of graphite to diamond in ureilites, which happened when the ureilite parent body (UPB) was most likely destroyed by massive impact events. We present data for carbon aggregates from the highly shocked (U‐S6) Northwest Africa (NWA) 6871 and the medium shocked (U‐S3) NWA 3140. Both samples contain abundant carbon aggregates which were analyzed by X‐ray diffraction and micro‐Raman spectroscopy revealing the presence of close associations of (compressed) nanographite, micro‐ and nanodiamond, as well as Fe‐rich phases. Graphite and diamond in NWA 6871 show shock indicators that are absent in NWA 3140. Based on Raman geothermometry on graphite, we calculated mean temperatures of 1368 ± 120 °C and 1370 ± 120 °C for NWA 3140 and NWA 6871, respectively. For comparison, a geothermometer based on the partitioning of Cr between olivine and low‐Ca pyroxene was applied on NWA 3140, which yielded a temperature of only 1215 ± 16 °C. The graphite‐based temperatures are the highest reported for graphite in ureilites so far and exceed calculated magmatic temperatures for ureilites from silicate‐ and chromite‐based geothermometers. Graphite temperatures fall into the temperature field of catalytic diamond synthesis, which supports the hypothesis of direct transformation from graphite to diamond upon shock. Although the temperatures estimated seem to be independent of the shock degree, they can be ascribed to the shock event that destroyed the UPB.

The first main group ureilite with primary plagioclase: A missing link in the differentiation of the ureilite parent body

AbstractMS‐MU‐012, a 15.5 g clast from the Almahata Sitta polymict ureilite, is the first known plagioclase‐bearing main group ureilite. It is a coarse‐grained (up to 4 mm), equilibrated assemblage of 52% olivine (Fo 88), 13% orthopyroxene (Mg# 89.2, Wo 4.5), 11% augite (Mg# 90.2, Wo 37.3), and 14% plagioclase (An 68), plus minor metal and sulfide. The plagioclase grains have been secondarily remelted and internally recrystallized, but retain primary external morphologies. Melt inclusions occur in olivine. Rounded chadocrysts of olivine and orthopyroxene are enclosed in augite grains. In terms of texture, mineralogy, major and minor element mineral compositions, and oxygen isotopes, MS‐MU‐012 is virtually identical to the archetypal Hughes‐type main group ureilites, with the significant addition of primary plagioclase. We conclude that MS‐MU‐012 formed as a cumulate in a common lithologic unit with the Hughes‐type ureilites. Based on reconstructed compositions of melts trapped in olivine, orthopyroxene, and augite in the Hughes‐type samples, we infer that the parent magma of the Hughes unit originated as a late melt in the incremental melting of the ureilite parent body (UPB), near the end of the melting sequence, but was not completely extracted from the mantle like earlier melts and was emplaced in an intrusive body. MELTS calculations indicate that olivine began to crystallize at ~1260 °C, followed shortly thereafter by co‐crystallization of orthopyroxene and augite. Plagioclase began to crystallize at ~1170–1180 °C. Graphite was buoyant in the melt and became heterogeneously distributed in flotation cumulates. Residual silicate liquid was extracted from the cumulate pile and could have crystallized to form the “labradoritic melt lithology” (with plagioclase of An ~68‐35), which is partially preserved as clasts in polymict ureilites. The final equilibration temperature recorded by the Hughes unit was ~1140–1170 °C, just before catastrophic disruption of the UPB. MS‐MU‐012 provides a critical missing link in the differentiation history of this asteroid.

Detection of Cosmic Fullerenes in the Almahata Sitta Meteorite: Are They an Interstellar Heritage?

Buckminsterfullerene, C60, is the largest molecule observed to date in interstellar and circumstellar environments. The mechanism of formation of this molecule is actively debated. Despite targeted searches in primitive carbonaceous chondrites, no unambiguous detection of C60 in a meteorite has been reported to date. Here we report the first firm detection of fullerenes, from C30 to at least C100, in the Almahata Sitta (AhS) polymict ureilite meteorite. This detection was achieved using highly sensitive laser desorption laser ionization mass spectrometry. Fullerenes have been unambiguously detected in seven clasts of AhS ureilites. Molecular family analysis shows that fullerenes are from a different reservoir compared to the polycyclic aromatic hydrocarbons detected in the same samples. The fullerene family correlates best with carbon clusters, some of which may have been formed by the destruction of solid carbon phases by the impacting laser. We show that the detected fullerenes are not formed in this way. We suggest that fullerenes are an intrinsic component of a specific carbon phase that has yet to be identified. The nondetection of fullerenes in the Murchison and Allende bulk samples, while using the same experimental conditions, suggests that this phase is absent or less abundant in these primitive chondrites. The former case would support the formation of fullerenes by shock-wave processing of carbonaceous phases in the ureilite parent body. However, there are no experimental data to support this scenario. This leaves open the possibility that fullerenes are an interstellar heritage and a messenger of interstellar processes.

Nickel and Chromium Stable Isotopic Composition of Ureilites: Implications for the Earth's Core Formation and Differentiation of the Ureilite Parent Body

AbstractWe report the first Ni and Cr stable isotope data for ureilite meteorites that are the mantle residue of a carbon‐rich differentiated planet. Ureilites have similar Ni stable isotope compositions as chondrites, suggesting that the core‐mantle differentiation of ureilite parent body (UPB) did not fractionate Ni isotopes. Since the size of Earth is potentially larger than that of UPB; with diameter &gt;690 km), resulting in higher temperatures at the core‐mantle boundary of Earth, it can be predicted that the terrestrial core formation may not directly cause Ni stable isotope fractionation. On the other hand, we also report high‐precision Cr stable isotope composition of ureilites, including one ureilitic trachyandesite (ALM‐A) that is enriched in lighter Cr stable isotopes relative to the main‐group ureilites, which suggests that the partial melting occurred on UPB. The globally heavy Cr in the UPB compared to chondrites can be caused by sulfur‐rich core formation processes.

Xenoliths in ordinary chondrites and ureilites: Implications for early solar system dynamics

AbstractForeign clasts (xenoliths) in meteoritic breccias are a serendipitous source of information about the impact environment in which their hosts formed, including impactor flux and cosmochemical types. These parameters may be related to timing and/or heliocentric distance of xenolith origin and implantation, and thus can be used to test or inform models of early solar system dynamics. We use xenoliths in ordinary chondrites (OCs) and ureilites to do this. We first conducted a petrologic and oxygen isotope study of a new, cm‐sized igneous‐textured clast in L3.7 Northwest Africa (NWA) 092, which highlighted some of the difficulties of identifying xenoliths in meteorites. Results indicate that this clast is not a xenolith but an impact melt of non‐local OC material. We add this result to a literature survey of more than 3000 OCs and find that the fraction of OCs that contain xenoliths is &lt;&lt;1%, and, even in these, the abundance and the diversity of xenoliths are very low. This contrasts markedly with the ureilites, ˜5% of which contain ˜1–10 vol% xenoliths from every major meteorite class, including multiple groups and petrologic types. To investigate reasons for this difference, we compare the histories of OC and ureilite parent bodies. The OC and ureilitic parent bodies accreted in the inner solar system within ˜1 AU of one another. The OC bodies accreted ˜2–3 Myr after calcium‐aluminum‐rich inclusion (CAI) formation and were heated slowly, experiencing thermal metamorphism over ˜50–60 Myr. The ureilite parent body (UPB) accreted &lt;1 Myr after CAIs and was heated rapidly, experiencing partial melting over ˜4 Myr. Both OC parent bodies and the UPB were catastrophically disrupted and reassembled into rubble piles. For ureilites, this occurred ˜5.0–5.4 Ma after CAIs, while for OCs, it did not occur until 50–60 Myr after CAIs. Xenoliths in OC and ureilitic breccias were acquired as fragments of impactors on the rubble piles. The presence in polymict ureilites of xenoliths of all OC groups (H, L, LL) and petrologic types (3–6), and the intimate scale on which these and myriad other xenolith types are mixed, indicate that most xenoliths were acquired within a short time period around ˜50–60 Myr after CAIs when OC (likely also Rumuruti chondrite and enstatite chondrite) parent bodies were disrupted. This timing is consistent with the early instability dynamical model for a period of excitation in the asteroid belt. Outer solar system (CC) xenoliths were also acquired during this period, but were derived indirectly from C‐type bodies that had already been emplaced in orbits in the asteroid belt. The large discrepancy in xenolith abundance between ureilites and OC may be due to different physical properties of their regoliths at 50–60 Myr after CAIs. CC‐like xenoliths in OC may represent a different, more recently acquired, population than those in polymict ureilites.

Origin of micrometer-sized impact diamonds in ureilites by catalytic growth involving Fe-Ni-silicide: The example of Kenna meteorite

The occurrence of shock-induced diamonds in ureilite meteorites is common and is used to constrain the history of the ureilite parent bodies. We have investigated a fragment of the Kenna ureilite by micro-X-ray diffraction, micro-Raman spectroscopy and scanning electron microscopy to characterize its carbon phases. In addition to olivine and pigeonite, within the carbon-bearing areas, we identified microdiamonds (up to about 10 μm in size), nanographite and magnetite. The shock features observed in the silicate minerals and the presence of microdiamonds and nanographite indicate that Kenna underwent a shock event with a peak pressure of at least 15 GPa. Temperatures estimated using a graphite geothermometer are close to 1180 °C. Thus, Kenna is a medium-shocked ureilite, yet it contains microdiamonds, which are typically found in highly shocked carbon-bearing meteorites, instead of the more common nanodiamonds. This can be explained by a relatively long shock event duration (in the order of 4–5 s) and/or by the catalytic effect of Fe-Ni alloys known to favour the crystallization of diamonds. For the first time in a ureilite, carletonmooreite with formula Ni3Si and grain size near 4–7 nm, was found. The presence of nanocrystalline carletonmooreite provides further evidence to support the hypothesis of the catalytic involvement of Fe-Ni bearing phases into the growth process of diamond from graphite during shock events in the ureilite parent body, enabling the formation of micrometer-sized diamond crystals.

Graphite-Based Geothermometry on Almahata Sitta Ureilitic Meteorites.

The thermal history of carbon phases, including graphite and diamond, in the ureilite meteorites has implications for the formation, igneous evolution, and impact disruption of their parent body early in the history of the Solar System. Geothermometry data were obtained by micro-Raman spectroscopy on graphite in Almahata Sitta (AhS) ureilites AhS 72, AhS 209b and AhS A135A from the University of Khartoum collection. In these samples, graphite shows G-band peak centers between 1578 and 1585 cm−1 and the full width at half maximum values correspond to a crystallization temperature of 1266 °C for graphite for AhS 209b, 1242 °C for AhS 72, and 1332 °C for AhS A135A. Recent work on AhS 72 and AhS 209b has shown graphite associated with nanodiamonds and argued that this assemblage formed due to an impact-event. Our samples show disordered graphite with a crystalline domain size ranging between about 70 and 140 nm. The nanometric grain-size of the recrystallized graphite indicates that it records a shock event and thus argues that the temperatures we obtained are related to such an event, rather than the primary igneous processing of the ureilite parent body.

Incremental melting in the ureilite parent body: Initial composition, melting temperatures, and melt compositions

AbstractUreilites are carbon‐rich ultramafic achondrites that have been heated above the silicate solidus, do not contain plagioclase, and represent the melting residues of an unknown planetesimal (i.e., the ureilite parent body, UPB). Melting residues identical to pigeonite‐olivine ureilites (representing 80% of ureilites) have been produced in batch melting experiments of chondritic materials not depleted in alkali elements relative to the Sun’s photosphere (e.g., CI, H, LL chondrites), but only in a relatively narrow range of temperature (1120 ºC–1180 ºC). However, many ureilites are thought to have formed at higher temperature (1200 ºC–1280 ºC). New experiments, described in this study, show that pigeonite can persist at higher temperature (up to 1280 ºC) when CI and LL chondrites are melted incrementally and while partial melts are progressively extracted. The melt productivity decreases dramatically after the exhaustion of plagioclase with only 5–9 wt% melt being generated between 1120 ºC and 1280 ºC. The relative proportion of pyroxene and olivine in experiments is compared to 12 ureilites, analyzed for this study, together with ureilites described in the literature to constrain the initial Mg/Si ratio of the UPB (0.98–1.05). Experiments are also used to develop a new thermometer based on the partitioning of Cr between olivine and low‐Ca pyroxene that is applicable to all ureilites. The equilibration temperature of ureilites increases with decreasing Al2O3and Wo contents of pyroxene and decreasing bulk REE concentrations. The UPB melted incrementally, at differentfO2, and did not cool significantly (0 ºC–30 ºC) prior to its disruption. It remained isotopically heterogenous, but the initial concentration of major elements (SiO2, MgO, CaO, Al2O3, alkali elements) was similar in the different mantle reservoirs.

Chromium Isotopic Constraints on the Origin of the Ureilite Parent Body

Abstract We report on the mass-independent Cr isotope compositions of 11 main group ureilites and an ureilitic trachyandesite (ALM-A). The 54Cr/52Cr ratios for main group ureilites vary from −1.06 ± 0.04 to −0.78 ± 0.05 and averaged at −0.91 ± 0.15 (2SD, N = 18) including the data from literature. We argue that this variation reflects primitive mantle heterogeneities within the ureilite parent body (UPB). As such, this body did not experience a global-scale magma ocean, which is consistent with heterogeneous O isotope in ureilites. Furthermore, the ε 54Cr values, Mn/Cr ratios, C isotope ratios, Mg# values, and Fe/Mn ratios in the olivine cores of ureilites are correlated with each other, which suggests the mixing of ureilite precursors from at least two reservoirs, rather than a smelting process or the oxidation from ice melting. All the ureilite samples (including the ALM-A) fall on a well-defined 53Mn–53Cr isochron corresponding to a 53Mn/55Mn ratio of (6.02 ± 1.59) × 10−6, which translates to an age of 4566.7 ± 1.5 Ma (within 2 Ma after calcium-aluminum-rich inclusions; CAIs) when anchored to the U-corrected Pb–Pb age for the D’Orbigny angrite. This old age indicates early partial melting on the UPB, consistent with the early accretion of the UPB (within 1 Ma after CAIs) predicted by thermal modeling. Furthermore, there is a 4∼5 Ma age difference between the external isochron in this study and internal isochron ages for the feldspathic clasts in polymict ureilites, which likely reflects an impact history during the early evolution of the UPB.

Noble gas variations in ureilites and their implications for ureilite parent body formation

Ureilites are equilibrated carbon-rich olivine-pyroxene rocks from the partially melted mantle of a large (>500 km diameter) heterogeneous parent body. Recently the ureilite parent body was interpreted as an incomplete mixture of material from two carbon-rich chondritic reservoirs, one (Mg-rich) with reduced iron, low Δ17O and low δ13C, and the other with oxidised iron, high Δ17O and high δ13C. Here we analyse noble gases (Ar, Kr and Xe) in six equilibrated (unbrecciated) ureilites from Northwest Africa (NWA 2236, NWA 7686, NWA 8049, NWA 8172, NWA 11032 and NWA 11368). We observe weak positive and negative correlations of Δ17O and Mg# with the elemental ratios of Ar/Xe and Kr/Xe, respectively, as well as a weak positive correlation of Mg# with the heavy isotopes of Xe. These correlations broadly support the idea of the two-component mixing hypothesis. Our analyses further suggest that the Mg-rich endmember was rich in Xe from presolar grains (HL-Xe) while the Mg-poorer component may have contained solar-derived noble gases. The observed correlations are less straightforward to reconcile with a recent model for the origin of the ureilite parent body, involving oxidation of metal by H2O from accreted ice with ‘heavy’ oxygen isotopes.

The origin of iron silicides in ureilite meteorites

Ureilite meteorites contain iron silicide minerals including suessite (Fe,Ni)3Si, hapkeite (Fe2Si) and xifengite (Fe5Si3). Despite occurring mostly in brecciated varieties presumed to be derived from the regolith of the ureilite parent asteroid, suessite has also been confirmed in one lithology of a dimict ureilite (NWA 1241). In contrast, Si-bearing Fe-metals occur in both brecciated and unbrecciated ureilites, implying that they were formed throughout the ureilite parent asteroid. We examined major, minor and trace element data of Fe-metals in seven brecciated ureilites (DaG 319, DaG 999, DaG 1000, DaG 1023, DaG 1047, EET 83309, and EET 87720) in addition to the dimict ureilite NWA 1241.In this study we show that the silicides and Si-bearing metals in ureilites have similar siderophile trace element patterns; therefore, the precursors to the silicides were indigenous to the ureilite parent body. Si-free kamacite grains in brecciated ureilites show flatter, more chondritic siderophile element patterns. They may also be derived from the interior of the ureilite parent body, but some may be of exogenous origin (impactor debris), as are rare taenite grains.On Earth, iron silicides are often formed under high-temperature and strongly reducing conditions (e.g. blast furnaces, lightning strikes). On the Moon, hapkeite (Fe2Si) and other silicides have been found in the regolith where they were formed by impact-induced space weathering. In the Stardust aerogel, iron silicides derived from comet Wild2 were also formed by an impact-related reduction process. Silicides in ureilite regolith breccias may have formed by similar processes but ureilites additionally contain abundant elemental carbon which probably acted as a reducing agent, thus larger and more abundant silicide grains were formed than in the lunar regolith or cometary material. The origin of suessite in NWA 1241 may be analogous to that of reduced lithologies in the terrestrial mantle, although a regolith origin may also be possible since this sample is shown here to be a dimict breccia.

Zinc isotopic variations in ureilites

Abstract The Ureilite Parent Body (UPB) was a C-rich planetary embryo disrupted by impact. Ureilites are fragments of the UPB mantle and among the most numerous achondrites. Zinc isotopic data are presented for 26 unbrecciated ureilites and a trachyandesite (ALM-A) from the same parent body. The δ66Zn values of ureilites range from 0.40 to 2.71‰ including literature results. Zinc isotopic compositions do not correlate with the compositions of olivine cores, with C and O isotopic compositions, with Zn abundances, nor with shock grades. The wide range of δ66Zn displayed by the ureilites is chiefly explained by evaporation processes that took place during the catastrophic breakup of the UPB. During breakup, the high temperatures of the UPB mantle allowed Zn to evaporate, regardless of the intensity the shock suffered by the ureilitic debris. For the most shocked of them, post-shock heating permitted greater evaporation, and heavier Zn isotopic compositions. The surface of the UPB was certainly much colder than the mantle before the breakup. Therefore, crustal rocks were probably less prone to Zn evaporation. ALM-A, the sole crustal rock analyzed at present, has a δ66Zn value (0.67‰) significantly higher than those of regular chondrites. This result indicates that its mantle source displayed already non-chondritic Zn isotopic compositions before the breakup of the UPB.