Search

Achondrite meteorites are remnants of the earliest planetary differentiation processes in the Solar System. They have been used to anchor short-lived radiochronometers to absolute ages determined from long-lived radiochronometers. More specifically, when comparing the isotopic systematics of the shortlived 26Al-26Mg chronometer anchored to absolute U-corrected Pb-Pb ages, inferences about the distribution of 26Al (half-life of 717 000 yr) in the protoplanetary disk can be evaluated. The ungrouped achondrite Erg Chech (EC) 002 has a distinct mineralogy and more evolved elemental composition compared to basaltic achondrites. In situ and solution 26Al-26Mg chronometry and 53Mn-53Cr chronometry suggest that EC 002 formed within 0.7 to 2.2 Ma after the formation of Ca-Al-rich inclusions (CAIs), making it the oldest known sample of igneous crust in the Solar System (Barrat et al., 2021; Anand et al., 2022; Zhu et al., 2022; Fang et al., 2022). Here we present the U-corrected Pb-Pb age and 26Al-26Mg age obtained by MC-ICPMS solution analysis of the same mineral separate samples of EC 002. In addition, six merrillite grains were analyzed by in-situ SIMS to determine their Pb-Pb individual ages. The U isotope composition of EC 002 exhibits internal heterogeneities between leached pyroxene (238U/235U = 137.766 ± 0.027) and the bulk rock (238U/235U = 137.8190 ± 0.0074). The Pb isotope composition of progressively leached pyroxenes are characterized by radiogenic 206Pb/204Pb ratios (ranging from 41 to 23487). Using the U isotope composition of the leached pyroxenes, the resulting age of the 207Pb/206Pb-204Pb/206Pb isochron is 4565.87 ± 0.30 Ma (2r). The weighted mean of the Pb-Pb ages of seven SIMS analyses of merrillites are 4564.3 ± 5.2 Ma (2r). These similar ages (within uncertainty) indicate rapid cooling and the absence of significant thermal events after 4559 Ma on the parent body of EC 002. The 26Al-26Mg isochron through a bulk rock, pyroxene, fine-rained and four plagioclase fractions defines an initial 26Al/27Al ratio of [8.89 ± 0.79] 106 corresponding to a formation age of 1.83 ± 0.12 Ma after CAIs ([5.23 ± 0.13] 105; Jacobsen et al., 2008). The initial 26Al abundance is consistent with previous MC-ICP-MS 26Al-26Mg reported systematics for EC 002 (Fang et al., 2022), but 0.46 ± 0.13 Myr older than the in situ SIMS 26Al-26Mg age previously reported by Barrat et al. (2021).When anchored to the absolute Pb-Pb age of CV3 CAIs (4567.30 ± 0.16 Ma; Connelly et al., 2012), the Al-Mg model age of EC 002 is 4565.47 ± 0.20 Ma, slightly younger than its U-corrected Pb-Pb age.

We conducted a petrologic study of apatite within eight unbrecciated, non-cumulate eucrites and two monomict, non-cumulate eucrites. These data were combined with previously published data to quantify the abundances of F, Cl, and H2O in the bulk silicate portion of asteroid 4 Vesta (BSV). Using a combination of apatite-based melt hygrometry/chlorometry and appropriately paired volatile/refractory element ratios, we determined that BSV has 3.0–7.2 ppm F, 0.39–1.8 ppm Cl, and 3.6–22 ppm H2O. The abundances of F and H2O are depleted in BSV relative to CI chondrites to a similar degree as F and H2O in the bulk silicate portion of the Moon. This degree of volatile depletion in BSV is similar to what has been determined previously for many moderately volatile elements in 4 Vesta (e.g., Na, K, Zn, Rb, Cs, and Pb). In contrast, Cl is depleted in 4 Vesta by a greater degree than what is recorded in samples from Earth or the Moon. Based on the Cl-isotopic compositions of eucrites and the bulk rock Cl/F ratios determined in this study, the eucrites likely formed through serial magmatism of a mantle with heterogeneous δ37Cl and Cl/F, not as extracts from a partially crystallized global magma ocean. Furthermore, the volatile depletion and Cl-isotopic heterogeneity recorded in eucrites is likely inherited, at least in part, from the precursor materials that accreted to form 4 Vesta and is unlikely to have resulted solely from degassing of a global magma ocean, magmatic degassing of eucrite melts, and/or volatile loss during thermal metamorphism. Although our results can be reconciled with the past presence of wide-scale melting on 4 Vesta (i.e., a partial magma ocean), any future models for eucrite petrogenesis involving a global magma ocean would need to account for the preservation of a heterogeneous eucrite source with respect to Cl/F ratios and Cl isotopes.

Mantles of rocky planets are dominantly composed of olivine and its high-pressure polymorphs, according to seismic data of Earth’s interior, the mineralogy of natural samples, and modelling results. The missing mantle problem represents the paucity of olivine-rich material among meteorite samples and remote observation of asteroids, given how common differentiated planetesimals were in the early Solar System. Here we report the discovery of new olivine-rich meteorites that have asteroidal origins and are related to V-type asteroids or vestoids. Northwest Africa 12217, 12319, and 12562 are dunites and lherzolite cumulates that have siderophile element abundances consistent with origins on highly differentiated asteroidal bodies that experienced core formation, and with trace element and oxygen and chromium isotopic compositions associated with the howardite-eucrite-diogenite meteorites. These meteorites represent a step towards the end of the shortage of olivine-rich material, allowing for full examination of differentiation processes acting on planetesimals in the earliest epoch of the Solar System., Ultramafic olivine-rich achondrites provide insight into the missing mantle problem in the asteroid belt. The petrology and geochemistry of these samples suggests they are related to Vesta or the Vestoids.

Primitive achondrites derive from the residual mantle of incompletely differentiated planetesimals, from which partial silicate and metallic melts were extracted. As such, primitive achondrites are uniquely useful to examine the early stages of planetesimal melting and differentiation. To better understand this early melting and melt segregation as well as the nature of the melts involved, we obtained mass-dependent Ru isotopic compositions of 17 primitive achondrites, including winonaites, acapulcoite-lodranites, ureilites, brachinites, and two ungrouped samples. Most primitive achondrites with subchondritic Ru concentrations are characterized by heavy Ru isotopic compositions relative to chondrites, likely reflecting the extraction of isotopically light partial metallic melts. While the segregation of early-formed partial Fe-Ni-S melts likely had no effect on the Ru isotope compositions, the subsequent extraction of S-free partial metallic melts at higher temperatures provides a viable mechanism for producing the observed Ru isotopic fractionation and fractionated highly siderophile element ratios among primitive achondrites. Together, these observations indicate that differentiation of primitive achondrite parent bodies involved the segregation of distinct partial metallic melts over a range of temperatures, and that these melts ultimately formed a partial core with fractionated and light Ru isotopic composition. This contrasts with the unfractionated Ru isotope signatures previously estimated for bulk iron meteorite cores, which therefore indicates quantitative metal segregation during core formation in the iron meteorite parent bodies. The less efficient metal segregation in primitive achondrite parent bodies most likely reflects lower initial amounts of heat-producing 26Al due to later accretion or impact disruption of the parent bodies during differentiation.

© The Meteoritical Society, 2020. Ureilites 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 Al2O3 and Wo contents of pyroxene and decreasing bulk REE concentrations. The UPB melted incrementally, at different fO2, 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.

Although pure metallic iron (i.e. that with an Fe content of greater than 99%) commonly occurs in achondrites, and within the returned soil from asteroids or the Lunar surface, it is rarely found in ordinary chondrites meteorites. Abundant nanophase iron particles (np-Fe0) were identified in pyroxene glass, within the shock melt vein of Grove Mountains (GRV) 022115, which is an ordinary (L6) chondrite, with a shock stage determined as S5. The association of np-Fe0, highly defective high pressure clinoenstatite (HP-CEn), silica glass, as well as vesicles, embedded in a pyroxene glass selvage within the shock melt vein in this meteorite suggests that these phases formed as the result of decomposition of the host pyroxene grain, a process induced by the shock event that affected GRV 022115. The reaction to account for this mineral breakdown can be written as: FeSiO3 → Fe + SiO2 + 1/2O2 ↑ (MgSiO3 remain in the HP-CEn). The pressure and temperature condition attending this reaction are estimated at 20–23 GPa and over 1800 °C, as indicated by the surrounded high-pressure mineral assemblage: ringwoodite, majorite, and magnesiowustite. This study provides evidence to the formation of np-Fe0 derived from pyroxene, and HP-CEn quenched metastably in such shocked vein could preserve the metastable phase transitions history record.

Volatile-rich, CI- and CM-like clasts occur in different brecciated achondrite and chondrite groups. The CI-like clasts in HEDs, polymict ureilites, as well as ordinary, CR, and CB chondrites have a similar mineralogy, indicating a similar alteration history. However, when viewed in detail, their mineral chemistry shows some minor differences between the clasts from different meteorite groups. For CM-like clasts found in HED meteorites, the clasts are, based on their mineralogy, clearly fragments of CM chondrites. To be able to decipher whether CI- (or CM-)like clasts from different meteorite groups are related to certain meteorite classes known to contain volatiles, we obtained D/H ratios of several clasts from the meteorite groups mentioned above and compared them with those of CI and CM chondrites as well as to unique carbonaceous chondrites such as Bells, Essebi, and Tagish Lake. Considering the δD-values, CM-like clasts in HEDs span a similar range compared to bulk values of CM chondrites, further indicating that CM-like clasts are fragments of CM chondrites. For CI-like clasts a clear distinction can be made: While CI-like clasts in HEDs and ordinary chondrites show a very similar range in their δD-signatures compared to “common” CI chondrites, meaning that these clasts are likely related to CI chondrites, the CI-like clasts in polymict ureilites are enriched in D up to 3000‰; a similarly high enrichment is found for the CI-like clasts in CR chondrites. Thus, although the CI-like clasts in ureilites and CR chondrites likely experienced similar alteration histories as the CI-like clasts found in the other meteorite types, these clasts probably formed in a different region than the CI chondrites and, thus, are more accurately referred to as C1 clasts. Overall, the existence and isotopic signatures of the C1 clasts in several meteorite groups proves the existence of additional primitive, volatile-rich material in the (early) Solar System besides the matter we study as the CI, CM, and CR chondrites. This material was distributed throughout the Solar System very early and might have played an important role for the volatile inventory of the terrestrial planets.

Major processes affecting high field strength (HFSE) and rare earth (REE) element ratios in planetary basalts are degree of melting, separation of metal-sulfide melt fractions, addition and loss of silicate melt, ilmenite fractionation, and subduction. Fractional crystallization of planetary magma oceans has left a surviving imprint on only three bodies for which we have data: the Moon, Vesta, and the angrite parent body. Thorium mobilization in aqueous fluids may account for decoupling of Th and Nb in planetary systems, and this is especially notable on Earth but also possible on Mars, the Moon and some asteroids. On Earth, HFSE and REE ratios in young basalts characterize hydrated (HM), enriched (EM) and depleted (DM) mantle sources, associated with, respectively, subduction, mantle plumes and ocean ridges. Terrestrial hydrated and depleted mantle were in existence by at least 4 Ga and possibly they may have been produced in a stagnant lid tectonic regime before 3 Ga. Also, removal of Nb in metal-sulfide melts can force the composition of silicate restitic material into the hydrated mantle field on HFSE-REE graphs, thus not requiring hydration. Such an origin is probable for “hydrated” mantle in primitive achondrites and plutonic angrites. The record of all three types of mantle in basalts from other bodies in the Solar System indicates the three mantle reservoirs are not diagnostic of plate tectonics, but can be produced in stagnant lid settings. Enriched mantle is thus far recognized only in Earth and possibly Mars. There are at least two enriched mantle reservoirs in Earth: a primordial (>4 Ga) reservoir, perhaps hidden in the D” layer above the core and rarely sampled by basalts, and a recycled plate reservoir ( Although there are several processes by which Nb can be fractionated from Ta in planetary bodies, the low Nb/Ta (

Ferrous oxide (FeO)-rich asteroid achondrites can be defined as asteroid-derived samples that experienced incipient partial melting processes in the early Solar System (>4.5 Ga) leading to melt-residues and cumulate and melt rocks that have high FeO in silicate grains (molar Mg/[Mg + Fe]

A late afternoon in February 1971, a meteorite impacted the rooftop of a house in Tintigny village in southern Belgium. Confirmed as a possible meteorite by the schoolteacher, the meteorite and its fall story did not leave the village. Finally, 46 years after the fall event, we got the opportunity to study and characterize this meteorite. In this work, we give a detailed report on its textural, mineralogical, whole-rock elemental and oxygen isotopic composition. Officially named as Tintigny, we classified it as an achondrite from howardite-eucrite-diogenite (HED) clan and more precisely a polymict eucrite. A brecciated basaltic rock believed to be originated from the surface of V-type asteroids namely the asteroid 4-Vesta. Tintigny has recorded the evidence of the impact metamorphism and metasomatism processes active on its parent body. Tintigny is one of the 39 eucrite falls known to date, and one of the 11 eucrites occurred in Europe. It is the fifth officially recognized meteorite and the first achondrite from Belgium. This report shows the importance of studying and accessing such a meteorite for further cosmochemical and planetary investigations and enriching our knowledge on the formation of HED meteorites and their parent bodi(es). In addition, it brings the attention to its importance as a scientific heritage that has to be properly understood and safeguarded for the generations of scientists, scholar, and amateurs to come., info:eu-repo/semantics/published

Kapoeta is an achondrite meteorite containing mm-sized carbonaceous-chondrite inclusions that are thought to have been incorporated into its parent body by carbonaceous-chondrite impactors (mainly CM “Mighei-type” material). Two different samples (A and B) of the Kapoeta carbonaceous-chondrite materials are studied by Mossbauer spectroscopy at room temperature. The Mossbauer spectra are fitted with a combination of Fe2+ and Fe3+ quadrupole doublets using a Voigt-based function. The spectrum of sample A shows two Fe2+ doublets and one Fe3+ doublet, with Fe3+ accounting for 64% of the total spectral area, and are ascribed to hydrated phyllosilicates. Sample-B spectrum, on the other hand, shows three doublets that are due to Fe2+ only, and are attributed mainly to amorphous silicates (predominantly dehydrated amorphous phyllosilicates) and presence of small amounts of olivine. The results are compared with published Mossbauer data on carbonaceous chondrites, and discussed in relation to aqueous alteration that occurred in their parent bodies and the thermal history the Kapoeta meteorite.

International audience; Heterogeneity in isotopic compositions within the protoplanetary disc has been demonstrated for a number of elements measured in extra-terrestrial materials, mostly based on chondrite meteorite analyses. However, precise 182Hf-182W and 26Al-26Mg ages of iron meteorites, achondrites, and chondrules show that chondrites accreted later than achondrites and therefore do not strictly represent the early (145Nd/144Nd and 148Nd/144Nd ratios (3.9 145Nd < 11.0 and 9.1 148Nd < 17.9 in part per million deviation, or μiNd) compared to NC chondrites (2.7 145Nd < 3.3 and 2.2 148Nd < 8.1). Moreover, the three terrestrial planets for which we have samples available (Earth, Mars, and the Moon) as well as the silicate inclusions from the non-magmatic IIE iron meteorite Miles present a systematic deficit in μ145Nd and μ148Nd compared to early-formed NC achondrites. Unlike chondrites, the Nd anomalies in achondrites are not correlated to the heliocentric distance of accretion of their respective parent bodies as inferred from redox conditions. Chronological constraints on planetesimal accretion suggest that Nd (and other elements such as Mo and Zr) nucleosynthetic compositions of the inner part of the protoplanetary disc significantly changed around 1.5 Ma after Solar System formation due to thermal processing of dust in the protoplanetary disc. This relatively late event coincides with the beginning of chondrule formation or at least their preservation. Terrestrial planets formed subsequently by a complex accretion regime during several million years. Therefore, two scenarios are envisioned considering the reported Nd isotope composition of early planetesimals: 1) Terrestrial planets accreted mostly chondritic material similar in composition to enstatite chondrites, or 2) early planetesimals constitute substantial parts of terrestrial planets building blocks mixed with highly thermally processed material enriched in s-process, still unsampled by meteorites.

International audience; The composition of asteroids gives crucial insights into the formation and evolution of the Solar System. Although spectral surveys and spacecraft missions provide information on small bodies, many important analyses can only be performed in terrestrial laboratories. Meteorites represent our main source of samples of extraterrestrial material. Determining the source asteroids of these meteorites is crucial to interpret their analyses in the broader context of the inner Solar System. For now, the total number of parent bodies represented in our meteorites collection is estimated to about 150 parent bodies, of which 50 parent bodies represented by the poorly studied ungrouped chondrites. Linking ungrouped meteorites to their parent bodies is thus crucial to significantly increase our knowledge of asteroids. To this end, the petrography of 25 ungrouped chondrites and rare meteorite groups was studied, allowing grouping into 6 petrographic groups based on texture, mineralogy, and aqueous and thermal parent body processing. Then, we acquired visible-near-infrared (VIS-NIR) reflectance spectroscopy data of those 25 meteorites, in order to compare them to ground-based telescopic observations of asteroids. The reflectance spectra of meteorites were obtained on powdered samples, as usually done for such studies, but also on raw samples and polished sections. With asteroids surfaces being more complex than fine-grained regolith (e.g., asteroid (101955) Bennu), in particular near-Earth asteroids, the use of raw samples is a necessary addition for investigating parent bodies. Our results showed that sample preparation influences the shape of the spectra, and thus asteroid spectral matching, especially for carbonaceous chondrites. Overall, the petrographic groups defined initially coincide with reflectance spectral groups, with only few exceptions. The meteorite spectra were then compared with reference end-member spectra of asteroids taxonomy. We matched the 25 studied meteorites to asteroids types, using a qualitative match of the shape of the spectra, as well as a quantitative comparison of spectral parameters (bands positions, bands depths and slopes at 1 and 2 μm). We define links between some of the studied ungrouped chondrites and asteroid types that had no meteorite connection proposed before, such as some very primitive type 3.00 ungrouped chondrites to B-type or Cg-type asteroids. We also matched metamorphosed ungrouped carbonaceous chondrites to S-complex asteroids, suggesting that this complex is not only composed of ordinary chondrites or primitive achondrites, as previously established, but may also host carbonaceous chondrites. Conversely, some ungrouped chondrites could not be matched to any known asteroid type, showing that those are potential samples from yet unidentified asteroid types.

Almahata Sitta (AhS), an anomalous polymict ureilite, is the first meteorite observed to originate from a spectrally classified asteroid (2008 TC(3)). However, correlating properties of the meteorite with those of the asteroid is not straightforward because the AhS stones are diverse types. Of those studied prior to this work, 70–80% are ureilites (achondrites) and 20–30% are various types of chondrites. Asteroid 2008 TC(3) was a heterogeneous breccia that disintegrated in the atmosphere, with its clasts landing on Earth as individual stones and most of its mass lost. We describe AhS 91A and AhS 671, which are the first AhS stones to show contacts between ureilitic and chondritic materials and provide direct information about the structure and composition of asteroid 2008 TC(3). AhS 91A and AhS 671 are friable breccias, consisting of a C1 lithology that encloses rounded to angular clasts (

Acid leaching has been widely used in Pb–Pb chronology especially on meteorite samples, as it enhances the precision and accuracy of the chronology by separating radiogenic Pb from non-radiogenic Pb in the samples. Yet, the detailed mechanism of the radiogenic Pb separation remains elusive. Here we report scanning electron microscopy observations of acid-leached minerals from three achondrites that were previously analyzed for pyroxene Pb Pb dating (D'Orbigny, Ibitira and Northwest Africa 6704), and one stony‑iron meteorite (Brenham). Moreover, we present chemical analysis of acid leachates and residues of pyroxene and whole-rock fractions from the three achondrites using inductively coupled plasma mass spectrometry. The combined results reveal the resistance of minerals to acid treatments with HNO3, HCl, and HF and, in turn, allow us to explore the prospects and limitations of acid leaching for Pb Pb chronology. In particular, we show that (i) washing with dilute acids can efficiently liberate contaminant terrestrial Pb adsorbed on the mineral surface; (ii) hot and more concentrated (~6 M) HNO3 and HCl can separate pyroxenes from sulfides and anorthitic plagioclase that are highly enriched in initial non-radiogenic Pb; (iii) albitic plagioclase and pyroxenes show limited dissolution during the HNO3 and HCl treatments, but are progressively leached by hot 1 M HF, making it difficult to separate them from each other; and (iv) within single pyroxene grains having exsolved lamellar textures, high-Ca lamellae are more efficiently leached by the HF treatment than low-Ca ones. In the context of a two-stage Pb isotopic evolution model for pyroxene lamellae, we demonstrate that heterogeneous and incomplete dissolution of pyroxene lamellae with dilute HF can result in inaccurate Pb Pb age estimates. This may account for previously observed scattered Pb isotopic data for meteorite samples that were taken as evidence for isotope fractionation in a radiogenic Pb component during HF treatments.

Deciphering aspects of the solar system’s formation process and the origin of planetary bodies can be achieved by examining primitive solar system materials, as these materials reflect the early solar system composition and may represent the building blocks of planetary bodies. Along these lines, knowing the original composition of carbonaceous chondrite meteorites is a valuable asset for determining the conditions in the parent bodies where they formed. Therefore, to determine the key characteristics of the parent bodies from which the carbonaceous chondrites and primitive materials are derived, we examined chemical and sulfur isotope compositions of sulfides in CM, CI and C2ung carbonaceous chondrites as well as from CM- and CI-like volatile-rich clasts; such an investigation allows us to explore the origin of these sulfides and to determine the primordial S composition of their parent body source region. In this study, sulfides from 7 CM, CI, and C2ung carbonaceous chondrites and 16 chondritic and achondritic breccias containing volatile-rich clasts were analyzed by electron microprobe and SIMS. Different sulfides were found, which shows evidence of different formation origins. Based on compositions and exsolution textures, we suggest that one fraction of the sulfides in both clasts and chondrites formed at high temperatures prior to incorporation into the parent body. The other sulfides most likely have a secondary origin and precipitated during fluid–rock interaction. Furthermore, differences in the S isotopic signature of the sulfides in chondrites correlate with the degree of aqueous alteration of the carbonaceous host rocks (CM or CI). Studying the sulfides of the volatile-rich clasts in brecciated chondrites and achondrites, a similar fractionation cannot be seen. Even though the mineralogy of CI chondrites and CI-like clasts is similar, the sulfides in CI chondrites appear to be enriched in heavy isotopes compared to those in the clasts (δ34S + 1‰ (CI) vs −2‰ (CI-like clast). This could have been caused by different alteration conditions, or it represents a different sampling reservoir. In this study a large S isotopic fractionation between pentlandite and pyrrhotite was found in large primarily formed sulfides showing exsolution textures, indicating that pentlandite prefers to incorporate light S isotopes. Considering the S isotope composition of the exsolved phase which can be found in CM- and CI-like clasts, the pristine δ34S value of the original monosulfide solid solution (mss) is estimated to be ∼−2‰. This value possibly resembles the sampling reservoir from which the sulfides formed, indicating that both CM- and CI-like clasts derived from a similar reservoir, and this reservoir is different from the formation reservoir of the CI chondrites.

The ungrouped achondrite NWA 7325 is a cumulate olivine gabbro (Irving et al., 2013). It contains abundant and unique micro-inclusions of Ca-pyroxene (Bischoff et al., 2013) and spinel-like Al-Mg oxide (Goodrich et al., 2017) in plagioclase, indicating a remelting event induced either by impact (Goodrich et al., 2017) or by magma intrusion (Bischoff et al., 2013; Weber et al., 2016). In this work, a combined FIB-TEM study has been conducted on these micro-inclusions to address their petrogenesis and the related history of NWA 7325. TEM study revealed that micro-inclusions in the interiors of large plagioclase grains are Al-enriched spinel (Mg/Al atomic ratio: 0.03–0.4) with minor needle-like α-corundum, whereas those in the margins are predominantly Al-rich diopside (En44.5-46.6Fs1.2-1.5Wo31.2-36.7CaTs17.6-22.4) with minor forsterite (Fo94.6-94.7). The Mg/Al atomic ratios of the spinel micro-inclusions are negatively correlated with the distance away from the interface of plagioclase-pyroxene. Large plagioclase grains also exhibit a decrease in the Mg/Al atomic ratio from the rims to the cores. Based on the reaction texture at the interfaces of plagioclase-pyroxene, we infer that the Mg concentration gradient in large plagioclase grains could have resulted from Mg diffusion from the remelted rims of pyroxene into plagioclase. In addition, TEM observations showed that large plagioclase grains are not single crystals, but assemblages of submicron to micron-sized crystals. The preservation of Mg concentration gradients, submicron-sized polycrystalline plagioclases, and the consistent presence of micro-inclusions within large plagioclase grains likely indicate complete remelting of plagioclase and partial remelting of pyroxene (only rims of pyroxene with plagioclase) followed by fast cooling. We propose that micro-inclusions of diopside, forsterite, Al-rich spinel and corundum crystallized from the melt, which developed a Mg concentration gradient during the remelting of NWA 7325. The heating temperatures of pyroxene and plagioclase in the remelting event were estimated to be 1274–1327 °C and ≥1530 °C, respectively. A subsequent cooling rate of ∼500–650 °C/h at 1300 °C was found by fitting the measured Mg concentration gradient in large plagioclase grains with a Fick’s second law model that incorporated the diffusion coefficients of Mg in plagioclase-melt. These results are better explained by a shock event; a magmatic intrusion process is ruled out. To achieve the coexistence of shock-induced high temperature (≥1274 °C) in-situ melting and only undulatory extinction of forsterite grains, an ambient temperature of 1000–1100 °C in the surrounding, parent rock of NWA 7325 was required prior to impact. This work suggests a very early shock event when NWA 7325 was hot and buried in the crust of its parental planetesimal, which is a scenario consistent with its magma crystallization age (∼4.3 Ma after CAIs, e.g., Koefoed et al., 2016). This work also implies that impacts are a potential heat source for melting hot planetesimals in the early Solar System.

Given the compositional diversity of asteroids, and their distribution in space, it is impossible to consider returning samples from each one to establish their origin. However, the velocity and molecular composition of primary minerals, hydrated silicates, and organic materials can be determined by in situ dust detector instruments. Such instruments could sample the cloud of micrometer-scale particles shed by asteroids to provide direct links to known meteorite groups without returning the samples to terrestrial laboratories. We extend models of the measured lunar dust cloud from LADEE to show that the abundance of detectable impact-generated microsamples around asteroids is a function of the parent body radius, heliocentric distance, flyby distance, and speed. We use monte carlo modeling to show that several tens to hundreds of particles, if randomly ejected and detected during a flyby, would be a sufficient number to classify the parent body as an ordinary chondrite, basaltic achondrite, or other class of meteorite. Encountering and measuring microsamples shed from near-earth and main-belt asteroids, coupled with complementary imaging and multispectral measurements, could accomplish a thorough characterization of small, airless bodies., 19 pages, 3 Tables, 10 Figures, accepted May 30, 2019

Spectral observations of asteroid family members provide valuable information regarding parent body interiors, the origin and source regions of near-Earth asteroids, and the link between meteorites and their parent bodies. Asteroids of the Hungaria family represent some of the closest samples to the Earth from a collisional family (∼1.94 AU), permitting observations of smaller family fragments than accessible for Main Belt families. We have carried out a ground-based observational campaign entitled Hungaria Asteroid Region Telescopic Spectral Survey (HARTSS) to record reflectance spectra of these preserved samples from the inner-most regions of the primordial asteroid belt. During HARTSS phase one (Lucas et al. (2017). Icarus 291, 268–287) we found that ∼80% of the background population is comprised of stony S-complex asteroids that exhibit considerable spectral and mineralogical diversity. In HARTSS phase two, we turn our attention to family members to determine if the Hungaria collisional family is compositionally homogeneous or heterogeneous. We use taxonomic classification, geometric albedo (pv) estimates, and near-infrared (NIR) spectral properties to infer the composition of the family. During phase two of HARTSS we acquired NIR spectra of 50 new Hungarias (19 family; 31 background) with the SpeX spectrograph at NASA's Infrared Telescope Facility (IRTF) and with the NICS spectrograph at the Telescopio Nazionale Galileo (TNG). We analyzed X-type spectra for NIR color indices (0.85-J; J-K), and a subtle ∼0.9 µm absorption feature that may be attributed to Fe-poor orthopyroxene ± the sulfide mineral oldhamite. Surviving fragments of an asteroid collisional family typically exhibit similar taxonomies, albedos, and spectral properties. Spectral analysis of Hungaria family X-types and independently calculated WISE albedos for family members (average pv= 0.403; n = 192) is consistent with this scenario. Furthermore, about one-fourth of the background population exhibit similar spectral properties and albedos to family X-types. Spectral observations of 92 Hungaria region asteroids acquired during both phases of HARTSS uncover a compositionally-heterogeneous background population—including two rare olivine-dominated A-types and one apparent D-type interloper—and spectral homogeneity down to ∼2 km for collisional family members. Taxonomy, albedos, and spectral properties indicate that the Hungaria family progenitor was an igneous body that formed under reduced conditions, and was likely consistent in composition with the enstatite achondrite (i.e., aubrite) meteorite group.

Ureilites are the second largest group of achondrite meteorites but consensus is still lacking on the nature of their precursors, melting processes, and the genetic relationship between monomict ureilites and brecciated ureilites. The recently found ureilite Ramlat as Sahmah 517 is of special interest in this context. This meteorite lacks shock features in its primary silicates and belongs to a rare augite- and chromite-bearing subset of the monomict ferroan ureilites. It hosts abundant intergranular glass veinlets speckled with pyroxene and metal globules. Detailed petrographic investigations show that the Si-Al-rich glass represents quenched anatectic melt that was present prior to formation of the reduced olivine rims by incomplete low-pressure equilibration (smelting) of carbon and silicates. The melt facilitated smelting which, along with rapid crystallization of secondary pyroxene, modified the originally trachyandesitic melt. Melt-silicate equilibrium preceding these events is constrained by modelling using MELTS and the first reported in-situ measurements of LREE-enriched glass that is largely complementary to the depleted mafic silicates in monomict ureilites. The inferred major element composition of the partial melt that formed in RaS 517 is similar to that of trachyandesite in Almahata Sitta but RaS 517 lacks phosphates which are abundant in the Almahata Sitta trachyandesite and in alkali-rich feldspathic clasts in polymict ureilites. The LREE-depletion in the dominant monomict ferroan ureilite population can be explained by the formation of melt fractions similar to the glass in RaS 517 after initial rapid melting of phosphates. These finds provide evidence for a genetic relationship between ferroan ureilites and lithologies similar to the Almahata Sitta trachyandesite and further suggest that these ureilites formed by partial melting of P- and alkali-rich precursors with trace element concentrations similar to equilibrated ordinary chondrites. Quenched Si-Al-rich glass also occurs in magnesian ureilites but has lower concentrations of alkalis and LREE-depleted trace element signatures which can reflect more depleted compositions at the onset of partial melting. The evidence presented here favors a scenario in which the primary ureilite differentiation was driven by gradual heating from radioactive decay with resulting temperatures (>1100 °C) being maintained until disruption of the ureilite parent asteroid.

The achondrite Asuka 881394 has mineralogy broadly similar to that of eucrites but is isotopically, chemically and texturally distinct from them. Previous U-Pb chronology shows that it is very old; forming within the first 0.8 Ma of the formation of calcium-aluminum rich inclusions (CAIs). However, the age difference between Asuka 881394 and other very old Solar System materials (CAIs, quenched angrites) measured with the 26Al-26Mg and 53Mn-53Cr extinct radionuclide chronometers, and 207Pb/206Pb chronometer, is not the same. This could be interpreted to reflect heterogeneity in the distribution of 26Al and 53Mn in the early Solar System. Given the significant implications for the early Solar System chronology if 26Al and 53Mn are indeed heterogeneously distributed, in this study we further investigate the origin of Asuka 881394 and the apparent age discordance between short-lived and absolute chronometers, by focusing on measurement of its e54Cr composition, renewed measurements of the absolute Pb-Pb age and new, high precision measurements of its 26Al-26Mg systematics. New Cr isotope data places additional constraints on the origin of Asuka 881394; its e 54Cr value of −0.37 ± 0.10e is resolvable outside of uncertainty from HED meteorites (−0.72 ± 0.10e), reinforcing evidence from oxygen isotopic analyses that suggest it originated from a distinct parent body, unlikely to be 4 Vesta. New Pb-Pb analyses, combined with using a directly measured 238U/235U ratio for age calculation, result in a recalculated Pb-Pb age of 4564.95 ± 0.53 Ma, ∼1.5 Ma younger than the previously reported age. With this age Asuka 881394 remains one of the oldest known achondrites in our Solar System. New high precision 26Al-26Mg data produce an initial 26Al/27Al ratio of 1.48 ± 0.12 × 10−6, within error of previous data. This ratio corresponds to an Al-Mg age of 4563.69 ± 0.36 Ma or 4564.83 ± 0.21 Ma relative to CAIs and the D’Orbigny angrite, respectively. Thus, depending on which age anchor is used, the 26Al-26Mg age is either 1.26 Ma or 0.12 Ma younger than the new Pb-Pb age, the latter being unresolved within analytical uncertainty. Though a potential age discrepancy between 26Al-26Mg and Pb-Pb could be a result of heterogeneous distribution of 26Al, we demonstrate with our new high precision Mg isotope data, in conjunction with petrographic evidence, that the Mg isotope system has been disturbed in Asuka 881394. We suggest that the 26Al-26Mg system closed to diffusion after the U-Pb system, either due to slow cooling on the parent body or low-grade metamorphic re-equilibration of Mg. Thus, we can satisfactorily explain the observed age discrepancy between 26Al-26Mg and U-Pb systems in Asuka 881394 without invoking heterogeneous distribution of 26Al/27Al ratio in the early Solar System. Comparison of the Asuka 881394 data with that of other anomalous achondrites from distinct parent bodies suggests that these could also have evolved from a source region with a canonical 26Al/27Al ratio. Because these achondrites have significant differences in their e54Cr-Δ17O systematics, which could be indicative of location within the early protoplanetary disk, it is consistent with homogeneous distribution of 26Al in the early Solar System. Angrites remain an outlier; either because they evolved from a source with a lower 26Al/27Al ratio or because their 26Al-26Mg or Pb-Pb data are problematic. In either case, this suggests that basaltic angrites are questionable as the age anchor for the entire Solar System as a whole, and other very old, well preserved achondrites should be considered for that role.

Northwest Africa (NWA) 6704 is a unique achondrite characterized by a near-chondritic major element composition with a remarkably intact igneous texture. To investigate the origin of this unique achondrite, we have conducted a combined petrologic, chemical, and (187)Re–(187)Os, O, and Ti isotopic study. The meteorite consists of orthopyroxene megacrysts (En(55–57)Wo(3–4)Fs(40–42); Fe/Mn = 1.4) up to 1.7 cm in length with finer interstices of olivine (Fa(50–53); Fe/Mn = 1.1–2.1), chromite (Cr# ~ 0.94), awaruite, sulfides, plagioclase (Ab(92)An(5)Or(3)) and merrillite. The results of morphology, lattice orientation analysis, and mineral chemistry indicate that orthopyroxene megacrysts were originally hollow dendrites that most likely crystallized under high super-saturation and super-cooling conditions (1–10(2) °C/h), whereas the other phases crystallized between branches of the dendrites in the order of awaruite, chromite → olivine → merrillite → plagioclase. In spite of the inferred high supersaturation, the remarkably large size of orthopyroxene can be explained as a result of crystallization from a melt containing a limited number of nuclei that are preserved as orthopyroxene megacryst cores having high Mg# or including vermicular olivine. The Re–Os isotope data for bulk and metal fractions yield an isochron age of 4576 ± 250 Ma, consistent with only limited open system behavior of highly siderophile elements (HSE) since formation. The bulk chemical composition is characterized by broadly chondritic absolute abundances and only weakly fractionated chondrite-normalized patterns for HSE and rare earth elements (REE), together with substantial depletion of highly volatile elements relative to chondrites. The HSE and REE characteristics indicate that the parental melt and its protolith had not undergone significant segregation of metals, sulfides, or silicate minerals. These combined results suggest that a chondritic precursor to NWA 6704 was heated well above its liquidus temperature so that highly volatile elements were lost and the generated melt initially contained few nuclei of relict orthopyroxene, but the melting and subsequent crystallization took place on a timescale too short to allow magmatic differentiation. Such rapid melting and crystallization might occur as a result of impact on an undifferentiated asteroid. The O–Ti isotope systematics (Δ(17)O = −1.052 ± 0.004, 2 SD; ε(50)Ti = 2.28 ± 0.23, 2 SD) indicate that the NWA 6704 parent body sampled the same isotopic reservoirs in the solar nebula as the carbonaceous chondrite parent bodies. This is consistent with carbonaceous chondrite-like refractory element abundances and oxygen fugacity (FMQ = −2.6) in NWA 6704. Yet, the Si/Mg ratio of NWA 6704 is remarkably higher than those of carbonaceous chondrites, suggesting significant nebular fractionation of forsterite in its provenance.

Northwest Africa (NWA) 6704/6693 are medium- to coarse-grained achondrites with unique petrologic and geochemical traits that are distinct from the currently established meteorite groups. Here, we report on the extinct 26Al-26Mg and 53Mn-53Cr systems to establish fine-scale chronology of its formation and Cr and Ti isotopic anomalies to constrain the composition of the source reservoir of NWA 6704/6693. Excesses in the neutron-rich 54Cr and 50Ti isotopes, due to nucleosynthetic anomalies, separate NWA 6704/6693 from the vast majority of established achondrites and instead resemble the excesses seen among the carbonaceous chondrites; specifically, the CR-type chondrites. The excesses in these isotopes indicate a common feeding zone during accretion in the protoplanetary disk between the source of NWA 6704/6693 and that of the carbonaceous chondrites. The 26Al-26Mg data for pyroxene and plagioclase from NWA 6704 yield a (26Al/27Al)0 = (3.15 ± 0.38)×10−7 (MSWD = 0.49) and an initial δ26Mg∗ = −0.004 ± 0.005 at the time of isotopic closure. This initial (26Al/27Al)0 translates to an absolute age of 4563.14 ± 0.38 Ma, relative to the D’Orbigny angrite. However, given the potential heterogeneity of 26Al, the D’Orbigny angrite might not be a good age anchor for the purpose of calculating 26Al-26Mg ages. The 26Al-26Mg age relative to another carbonaceous achondrite, NWA 2976, is 4562.66 ± 0.60 Ma. The 53Mn-53Cr systematics of NWA 6704/6693 indicate a (53Mn/55Mn)0 of (2.59 ± 0.34) × 10−6 (MSWD = 1.2) with an evolved initial e53Cr of +0.14 ± 0.03. The (53Mn/55Mn)0 yields an 53Mn-53Cr age of 4562.17 ± 0.76 Ma relative to the D’Orbigny angrite. Concordant ages determined using the short-lived 26Al-26Mg and 53Mn-53Cr systems and extant 207Pb-206Pb system (4562.60 ± 0.30 Ma for NWA 6704/6693; Amelin et al., 2019) indicate rapid cooling and nearly contemporaneous closing of multiple isotope systems. The ancient crystallization ages and positive 54Cr and 50Ti anomalies of NWA 6704/6693 indicate widespread melting and differentiation processes occurring in both non-carbonaceous (NC) and carbonaceous chondrite (CC) regions of the protoplanetary disk. Additionally, we report the Cr and Ti isotopic composition for a petrologic range of CR-type materials (CR2, CR6, and achondrites). The additional Cr and Ti isotopic data for these CR-type materials indicates a range in isotopic composition not previously observed based on CR2 chondrites alone.

The angrites are a class of achondrites that encompass a wide range of igneous textures from quenched, volcanic, and subvolcanic stones to slowly cooled, plutonic rocks. The compositions of the various geochemical reservoirs generating this variety of rocks have not been investigated fully because historically the numbers and masses of angrites available for study have been quite small. However, the rapid increase in meteorites from Northwest Africa (NWA) has enabled a renewed opportunity for such an investigation. In particular, three samples, NWA 2999, 4590, and 4801, have provided a new window into our understanding of the origin and petrogenesis of the coarse-grained (plutonic) angrites. We report here the trace element abundances in individual mineral grains of pyroxene, plagioclase, olivine/kirschsteinite, and phosphate and in the whole-rock samples. We utilize these data to constrain the petrogenetic history of each of these samples on the angrite parent body (e.g., parental melt compositions and oxygen fugacity conditions) and assess genetic relationships to previously investigated angrites. The trace element abundances in each of the three coarse-grained angrites studied here indicate a unique history for each. The observed trace element abundances and patterns in NWA 2999 show similarities with previously studied fine-grained, volcanic angrites and potentially indicate a common geochemical source reservoir, even though NWA 2999 is temporally distinct from the volcanic angrites. In contrast, NWA 4590 has trace element characteristics analogous to other coarse-grained angrites (e.g., Lewis Cliff [LEW] 86010), suggesting that these samples originated from geochemically similar source reservoirs. The third angrite, NWA 4801, exhibits geochemical characteristics most similar to the plutonic, coarse-grained angrites, but also appears to have some affinities in its trace element characteristics to the volcanic, fine-grained angrites. This suggests that NWA 4801 may represent a petrogenetic link between two distinct geochemical reservoirs on the angrite parent body. In aggregate, the trace element distributions in these three plutonic angrites suggest that while they may have originated up to several million years after the fine-grained angrites, they sampled a range of source reservoirs on the angrite parent body. Some of these source reservoirs were likely similar to those of the fine-grained angrites, but others had distinct geochemical characteristics.

Northwest Africa (NWA) 11042 is a heavily shocked achondrite with medium-grained cumulate textures. Its olivine and pyroxene compositions, oxygen isotopic composition, and chromium isotopic composition are consistent with L chondrites. Sm-Nd dating of its primary phases shows a crystallization age of 4100 +/- 160 Ma. Ar-Ar dating of its shocked mineral maskelynite reveals an age of 484.0 +/- 1.5 Ma. This age coincides roughly with the breakup event of the L chondrite parent body evident in the shock ages of many L chondrites and the terrestrial record of fossil L chondritic chromite. NWA 11042 shows large depletions in siderophile elements (

New methods to determine the titanium (Ti) mass-dependent isotope fractionation of solar system materials to high precision were developed by combining internally normalised Ti isotope data with double-spike analyses utilising a 47Ti-49Ti double spike. The procedure includes a three-stage ion-exchange separation procedure to isolate Ti from the sample matrix that provides high-purity Ti fractions that are necessary for high-precision Ti isotope analyses. Analyses of sample aliquots that were spiked before and after the ion-exchange separation procedure demonstrate that Ti isotope fractionation can be induced by the separation procedure. This outcome requires the addition of the double spike before the ion exchange separation procedure in order to accurately determine the natural mass-dependent Ti isotope fractionation of samples. Multiple double spike analyses of an Alfa Aesar Ti standard performed over eight months yielded a reproducibility (2σ standard deviation) of 0.033‰ for δ49/47Ti (differences in 49Ti/47Ti relative to the OL-Ti standard). Terrestrial sample analyses display a 2σ reproducibility of 0.018 to 0.031‰ for δ49/47Ti. Titanium isotope results for three terrestrial USGS magmatic reference samples (AGV-2, BHVO-2 and BCR-2) agree well with literature data and therefore demonstrate the accuracy and precision of the presented methodologies. Achondritic meteorites display an overall range of 0.75‰ for δ49/47Ti. The ungrouped achondrite NWA 7325 has a more positive composition by 0.64‰ for δ49/47Ti compared to all other investigated samples likely reflecting Ti isotope fractionation induced by magmatic differentiation associated with highly reducing conditions and potentially associated with oxide and plagioclase formation. In contrast, eucrites with δ49/47Ti of -0.020 ± 0.070 and -0.003 ± 0.033 and the first mass-dependent Ti isotope data for an acapulcoite (Dhofar 125; δ49/47Ti = 0.094 ± 0.033) show only limited magmatic Ti isotope fractionation. Chondrites also display a relatively restricted range of 0.085‰ for δ49/47Ti, including one calcium aluminum rich inclusion (CAI) from Allende and the first mass-dependent Ti isotope data for two Rumuruti chondrites (NWA 753 and NWA 755). Furthermore, the mass-dependent Ti isotope composition of chondrites overlaps with that of eucrites and the acapulcoite Dhofar 125 indicating that nebular processes induce only limited Ti isotope fractionation. Additionally, the Ti isotope data indicate that thermal metamorphism also produced marginal Ti isotope fractionation at the bulk sample scale for chondrites. Small mass-dependent Ti isotope variations between different bulk meteorite samples are also evident, which might reflect sample heterogeneity. Importantly, the mass-dependent Ti isotope composition of the Earth and Moon overlap with the composition of the investigated chondrites, eucrites and acapulcoites within the 2 standard deviation uncertainties., Chemical Geology, 568, ISSN:0009-2541, ISSN:1872-6836

We report petrologic studies and oxygen isotope analyses of normal and anomalous eucrites, termed eucrite-type achondrites. Petrologically anomalous eucrite-type achondrites can have normal oxygen isotope compositions, and vice versa. Two basaltic eucrites with normal oxygen isotope compositions contain pyroxenes with anomalous Fe/Mn engendered by parent body processes acting on normal eucrites: solid-state reduction by S gas in EET 87542, and reduction during crystallization by magmatic S in QUE 94484. Cataclastic basaltic breccias PCA 82502 and PCA 91007 are paired (petrology, anomalous oxygen). Although isotopically like Pasamonte, they are petrologically distinct. We confirm the petrological and isotopic anomalies of cumulate gabbro EET 92023; likely formed by impact melting of mixed cumulate and basaltic materials. Many main group eucrites include plagioclases that retain near-liquidus compositions despite metamorphic overprinting. Stannern group eucrites contain more sodic plagioclase, which is consistent with the melt hybridization hypothesis for Stannern group magma formation. The lack of more calcic plagioclase suggests reactive exchange of the anorthite component of the primary melt with the albitic component of the crust. Asteroids that are modestly different in composition can produce virtually indistinguishable basalts, providing a ready explanation for the eucrite-type achondrite suite. Small stochastic variations in petrologic evolution can cause substantial differences in rocks produced on an asteroid.

In this presentation, we will summarize the conclusions of three recent articles [1-3] describing partial melting experiments of ordinary and carbonaceous synthetic chondrites (H, LL, CI, CM and CV). The experiments highlight the role of alkali elements on the melting processes of chondritic planetesimals and provide insights into the distribution of “moderately volatile elements” in the early solar system. They were performed at 2–13 MPa (CO pressure) in a Molybdenum-Hafnium Carbide Pressure Vessel. This approach prevented the loss of alkali elements during experiments, a common limitation of previous studies using gas-mixing furnaces. Alkali-rich planetesimals, similar in composition to CI, H and LL chondrites, started to melt at low temperature (1040 ºC) and produced silicate melts with high alkali, SiO2 and Al2O3 contents [1], similar in composition to “trachyandesite achondrites” such as GRA 06128 [4] and ALM-A [5]. In addition, the main groups of primitive achondrites (i.e., brachinites, acapulcoites-lodranites and ureilites), which represent mantle residues, all produced similar low-degree melts (2, Al2O3 and alkalis that were extracted from the mantle of the different parent bodies [2]. Ureilites (>550 samples), represent the residual mantle of a planetesimal that was catastrophically disrupted and quenched while in the process of melting [3]. Our experiments show that the Ureilite Parent Body (UPB) produced a total of 16-24 wt.% silicate melt as small increments (< 5%). Following the extraction of melts rich in SiO2, Al2O3 and alkalis, the residual mantle produced melts poor in alkalis but rich in CaO. The sampled portion of the UPB reached temperatures as high as 1300 ºC, but the rapid extraction of silicate melts preserved primordial heterogeneities in O, C and Cr isotopes as well as in intrinsic fO2. Trachyandesite achondrites, ureilites and other major groups of primitive achondrites were all derived from planetesimals that were initially rich in alkali elements (i.e., not depleted relative to the Sun’s photosphere). They all display nucleosynthetic anomalies characteristic of the inner solar system. Therefore, the depletion of alkalis in other meteorite parent bodies of the inner solar system (e.g., Vesta) likely results from processes that occurred during partial melting. Similarly, the depletion of alkalis in terrestrial planets could result from a secondary loss of alkalis associated with partial melting of the planets building blocks, rather than from the incomplete condensation of the solar nebula. References: [1] Collinet and Grove (2020a), GCA, https://doi.org/10.1016/j.gca.2020.03.005, [2] Collinet and Grove (2020b), GCA, https://doi.org/10.1016/j.gca.2020.03.004, [3] Collinet and Grove (2020c), MAPS, https://doi.org/10.1111/maps.13471, [4] Day et al., (2009), Nature, https://doi.org/10.1038/nature07651, [5] Bischoff et al. (2014), PNAS, https://doi.org/10.1073/pnas.1404799111

14th Europlanet Science Congress, The Moon is no longer a goal in itself but a necessary step for the conquest of space. In this work we focus in the composition of Lunar meteorites as the only objects alongside Apollo, and Luna collected samples, that the scientific community has available to first-hand analyze the Moon. Future Artemis sample return missions will provide new samples to continue learning from our satellite. Given its proximity to our planet, our satellite is an ideal planetary body to use it as a space camp for new technology, to establish a space base, and to test space mining. The continuous depletion of Earth resources put special importance on the exploration of extraterrestrial natural resources potential and the feasibility of its exploitation. After many robotic and manned missions, the utilization of lunar resources has been studied for a long time. In-Situ Resources Utilization (ISRU) refers to the generation of materials (for construction, life support, or as propellants) from the available resources on a celestial body that otherwise, would have needed to be brought from Earth, The authors acknowledge financial support from the Spanish Ministry (PGC2018-097374-B-I00).

Data on the chromium stable isotope composition of planetary reservoirs have the potential to provide information about core formation, partial melting and conditions of the Moon formation. In order to detect the small Cr isotopic differences between various reservoirs in the solar system, their compositions need to be precisely constrained. The current BSE value of δ53Cr = −0.11 ± 0.06‰ (Sossi et al., 2018) cannot resolve differences between achondrites, (Vesta δ53Cr = −0.17 ± 0.05‰) and chondrites (carbonaceous δ53Cr = −0.12 ± 0.05‰; ordinary δ53Cr = −0.11 ± 0.04‰). The composition of the bulk silicate Earth (BSE) is often used as a reference point for comparisons to other planetary reservoirs. However, past attempts to estimate the Cr isotopic composition of the BSE have been unable to provide a well-constrained BSE value. Traditional methods, using mantle peridotites, are affected by the susceptibility of Cr isotopes to fractionation during metasomatism. More recently, the Cr isotope composition of the BSE has been calculated using komatiites, in addition to mantle peridotites, to produce a more precise value (Sossi et al., 2018). In order to constrain the BSE composition to a higher precision, the δ53Cr of remarkably fresh komatiite lava flows from three localities, ranging in age from 2.7 Ga to 89 Ma, have been investigated in detail. These included the Tony's Flow in the Belingwe Greenstone Belt, Zimbabwe, the Victoria's Lava Lake in Fennoscandia, and komatiites from Gorgona Island in Colombia.\ud\udIn the komatiites studied, a range in Cr isotopic compositions was found, from δ53Cr = −0.16 ± 0.02 to −0.01 ± 0.02‰. We show that the high degrees of partial melting that produced the komatiites, did not result in Cr isotopic fractionation between the komatiitic melt and mantle residue. However, limited Cr isotopic fractionation is found to be a consequence of komatiite lava differentiation. For the lava flows with high Mg content and high Cr2+/ƩCrTOT (the molar ratio of Cr2+/(Cr2+ + Cr3+)), such as Tony's Flow and Gorgona, δ53Cr increases in the evolved portion of the magma during olivine fractionation due to the preferential inclusion of light Cr into olivine. Other flows with lower MgO content do not show this behaviour because a smaller fraction of the Cr is contained in olivine. The effects of fractional crystallisation must, therefore, be taken into account when calculating the Cr isotopic composition of the source of komatiite lavas.\ud\udThe weighted average of δ53Cr for the komatiite lavas analysed is −0.12 ± 0.04‰ (n = 5) and represents our best estimate for the Cr isotopic composition of the BSE. It agrees with the previous estimates, while providing an improvement to the uncertainty. There is no resolvable difference between this value and that of chondritic meteorites. Our data also indicate that the δ53Cr of the mantle has been constant since at least the Archean.