¹F. N. Lindsay et al. (>10)
Meteoritics & Planetary Science (in Press) Link to Article [https://doi.org/10.1111/maps.13637]
¹Department of Chemistry & Chemical Biology, Rutgers University, New Brunswick, New Jersey, 08854 USA
Published by arrangement with John Wiley & Sons

The Martian breccias NWA 7034, NWA 7533, and paired meteorites record events ranging in age from 4.47 Ga to <200 Ma. Published ages indicate a period of major disturbance at ~1.4 Ga, examined in detail here through 40Ar/39Ar dating of handpicked grains and two small chips. Argon diffusion parameters were obtained for six samples. Also presented are He, Ne, Ar, Kr, and Xe contents of two small (<100 µg), handpicked mineral separates, a felsic “Light” sample and a mafic/pyroxene‐rich “Dark” sample. The 40Ar/39Ar ages of five samples, four containing >1 wt% K and thought to be rich in feldspar and one containing <~1 wt% K, cluster near 1.4 Ga. The 40Ar/39Ar ages of nine grains with low K contents have a wide range of apparent ages from 0.3 ± 0.1 Ga to 2.9 ± 0.1 Ga for individual temperature steps, and from 0.74 ± 0.06 Ga to ~2.1 Ga for plateau ages. Isochron ages are less precise, but generally agree with plateau ages. Only two isochrons have the significantly positive intercepts expected in the presence of terrestrial or Martian atmospheric argon. At higher release temperatures, activation energies for diffusion obtained from 39Ar data for six samples are generally 160–200 kJ mol−1, consistent with published values for feldspathic minerals. For three of these samples, lower temperature data on Arrhenius plots are best fit with a much lower activation energy of <100 kJ mol−1. We attribute the low values to the effects of varying degrees of shock on feldspathic minerals and/or the presence of phases in vitrophyric spherules produced by hydrothermal alteration. The low activation energies place an upper limit of ~14 ka on the terrestrial age of NWA 7034. Much lower concentrations of cosmogenic (c) 3He and 21Ne in the Light than in the Dark separate indicate substantial losses concurrent with or postdating cosmic ray irradiation. A one‐stage, cosmic ray exposure (CRE) age for the Dark separate from NWA 7034 is estimated to be between 7 and 10 Ma from the concentrations of 3Hec and 38Arc, and of close to 15 Ma from the concentration of 21Nec. Most of the 40Ar/39Ar and noble gas data are compatible with (1) a heating and alteration event ~1.40 Ga caused by contact metamorphism, an impact, and/or the infiltration of hydrothermal fluids; and (2) at least one later event at lower temperatures that led to either loss of He and Ar from phases with low activation energies, or to gain of K. Most of the 40Ar/39Ar ages are consistent with the assembly of NWA 7034 1.4 Ga ago or perhaps earlier followed more recently by selective alteration. A more recent time of assembly is also consistent with these ages provided that the temperature stayed low. The five most precise 40Ar/39Ar ages of the samples analyzed are all ~1.4 Ga, a value seen frequently in other NWA 7034 chronometers and very similar to crystallization ages of nakhlites and chassignites (NC). Some CRE ages based on noble gases in NWA 7034 agree within their considerable uncertainties with those of NC. These two chronometric coincidences suggest that the NWA 7034 clan and the NC share a launch date on Mars. We propose that K‐rich fluids derived from the nakhlite source area interacted with proto‐NWA 7034 and modified the K/Ar ratios and ages of previously shocked feldspar grains, with the degree of modification depending on the degree of shock. The NWA 7034 clan may therefore be considered components from a metamorphic aureole around a nakhlite massif.

^1,2F. Jourdan,^2,3L. Forman,^1,2T. Kennedy,¹G. K. Benedix,⁴E. Eroglu,¹C. Mayers
Meteoritics & Planetary Science (in Press) Link to Article [https://doi.org/10.1111/maps.13640]
¹Western Australian Argon Isotope Facility, John de Laeter Centre, TIGeR, Curtin University, Perth, 6845 Western Australia, Australia
²Space Science and Technology Centre, School of Earth and Planetary Sciences, Curtin University, Perth, 6845 Western Australia, Australia
³Department of Earth & Planetary Sciences, Western Australian Museum, Locked Bag 49, Welshpool DC, Perth, 6986 Western Australia, Australia
⁴School of Molecular and Life Sciences, Curtin University, Perth, 6845 Western Australia, Australia
Published by arrangement with John Wiley & Sons

Asteroid 4 Vesta is the only largely preserved differentiated asteroid and thus is an excellent proxy to study early magmatism occurring on planets and moons. In this study, we focus on eucrite Pecora Escarpment (PCA) 82502, a medium‐ to fine‐grained eucrite which chemical analyses suggest belongs to the main howardite–eucrite–diogenite clan, albeit with some peculiarities. We carried out backscattered electron and electron backscattered diffraction microscopy analyses of the meteorite along with step‐heating 40Ar/39Ar dating analyses of various types of groundmass aliquots. We show that Pecora Escarpment 82502 is composed of medium‐grained igneous crystalline clasts and smaller fractured satellite clasts surrounded by approximately 50 µm wide impact melt veins of the same composition. Our results show that the large crystalline clasts and fine‐grained veins both display little evidence of shock processes. Six groundmass aliquots from large crystalline clasts returned concordant plateau (>70% of 39Ar) or mini‐plateau (50–70% of 39Ar) 40Ar/39Ar ages with a weighted mean of 4531 ± 6 Ma (P = 0.67). Thermodynamic cooling and 40Ar diffusion models suggest that the K/Ar system recorded and preserved the igneous age despite subsequent infiltration of hot and quickly quenched melt veins. Our new igneous age, combined with evidence for four other young volcanic and plutonic eucrites of similar age, shows that Vesta was still magmatically active around 4531 Ma. The lack of younger ages suggests that this age might well represent the end of the magmatic activity in the upper crust of Vesta. When combined with existing paleomagnetic constraints, our data suggest that 4 Vesta had an active dynamo that was still active ~35 Ma after accretion.

¹Robert W.Nicklas,¹James M.D.Day,²Zoltan Vaci,³Arya Udry,⁴Yang Liu,⁵Kimberly T.Tait
Earth and Planetary Science Letters 564, 116876 Link to Article [https://doi.org/10.1016/j.epsl.2021.116876]
¹Scripps Institution of Oceanography, University of California San Diego, La Jolla, CA, 92093, USA
²Institute of Meteoritics, Department of Earth and Planetary Science, University of New Mexico, Albuquerque, NM, 87131, USA
³Department of Geoscience, University of Nevada, Las Vegas, Las Vegas, NV 89154, USA
⁴Jet Propulsion Laboratory, California Institute of Technology, Pasadena, CA 91109, USA
⁵Department of Natural History, Royal Ontario Museum, Toronto, ON, M5S 2C6, Canada
Copyright Elsevier

Martian meteorites are the only available samples that can be directly measured to constrain the geological evolution of Mars. It has been suggested that the oxygen fugacity (fO2) of martian shergottite meteorites, which have low (∼7 wt.%) to high-MgO (∼30 wt.%) compositions, correlates with incompatible trace element enrichment (i.e., La/Yb), and 87Sr/86Sr, 143Nd/144Nd, 187Os/188Os and 176Hf/177Hf at the time of crystallization. These relationships have been interpreted to result from early magmatic processes segregating enriched and more oxidized from depleted and more reduced reservoirs in Mars. Here we use the V-in-olivine oxybarometer to constrain the fO2 of shergottites and the dunitic chassignites. These data, utilizing early crystallizing silicate phases, constrain the shergottite fO2 range to between −3.72 ± 0.07 and −0.21 ± 0.55 ΔFMQ (log units relative to the fayalite-magnetite-quartz buffer), with no correlation with trace element enrichment or Nd isotope systematics. Previously employed oxybarometers that use later-formed or multiple mineral phases, and that show such correlations, likely differ from the V-in-olivine oxybarometer in that they record effects from late-stage magmatic processes. In contrast to shergottites, chassignites are relatively oxidized, at +2.1 ± 0.4 to +2.2 ± 0.5 ΔFMQ. The chassignites, along with the nakhlites, have been proposed to be sourced from metasomatized lithospheric mantle, and their high fO2 strengthens this model. The new data implies that the martian mantle sources of shergottites have fO2 of −2.1 ± 1.8 ΔFMQ. This estimate indicates that the mantle and core of Mars are not in redox equilibrium and therefore that oxidation of the martian mantle following core formation is required.

¹Johan Vandenborre,³Laurent Truche,¹Amaury Costagliola,¹Emeline Craff,¹Guillaume Blain,¹Véronique Baty,²Ferid Haddad,²Massoud Fattahi
Earth and Planetary Science Letters 564, 116892 Link to Article [https://doi.org/10.1016/j.epsl.2021.116892]
¹Subatech, UMR 6457, Institut Mines-Télécom Atlantique, CNRS/IN2P3, Université de Nantes, 4, Rue Alfred Kastler, La chantrerie BP 20722, 44307 Nantes cedex 3, France
²GIP ARRONAX, 1 rue ARRONAX, CS 10112, 44817 Saint-Herblain Cedex, France
³University Grenoble Alpes, CNRS, ISTerre, CS 40700, 38058 Grenoble, France
Copyright Elsevier

Low molecular weight carboxylate anions such as formate (HCOO−), acetate (CH3COO−) and oxalate (C2O) have been shown to play an important role in supporting deep subsurface microbial ecosystems. Their origin whether biological or abiotic is currently highly debated, but surprisingly radiolytic production has rarely been considered, as it is the case for H2. Here, we address this question through dedicated irradiation experiments. Aqueous solutions containing carbonate, formate, acetate or oxalate have been irradiated using both the 60.7 MeV α-beam of the ARRONAX cyclotron (Nantes, France) and 661.7 keV γ-Ray in order to reveal the mechanism and chemical yield of radiation-induced dissolved carbonate degradation.

The yields (G-values) of carboxylate anions production/degradation in low-concentration carbonate solution (0.01 to 1 mmol L−1) are measured. Carbonate degradation occurs through three consecutive steps (Carbonate
Formate Acetate Oxalate) involving formate radical (CO2−•), dihydrogen (H2), and carbon dioxide (CO2) generation. Dissolved carbonate radiolysis provides a consistent pathway for both enhancing two-fold the radiolytic H2 production compared to pure water and generating carboxylic species, chiefly oxalate, readily available for microbes. Radiation-induced carbonate degradation may produce substantial amount (millimolar concentration) of carboxylate anions in ancient groundwaters from deep crystalline bedrocks. Subsurface lithoautotrophic microbial ecosystems may not only be supported by radiolytic H2 but also by carboxylate species from carbonate radiolysis. Carbonate radiolysis can be also an endogenous source of carboxylate species on Mars and other planetary bodies.

¹Caroline AVRIL,¹Valérie MALAVERGNE,²Eric D. VAN HULLEBUSCH,³Fabrice BRUNET,²Stephan BORENSZTAJN,⁴Jérôme LABANOWSKI,⁵Louis HENNET,⁶François GUYOT
Meteoritics & Planetary Science (in Press) Link to Article [https://doi.org/10.1111/maps.13641]
¹Laboratoire Géomatériaux et Environnement, Université Gustave Eiffel, EA 4508, UPEM, 5 boulevard Descartes, 77454 Marne‐la‐Vallée, Cedex 2, France
²Institut de physique du globe de Paris, CNRS, Université de Paris, F‐75005 Paris, France
³ISTerre, CNRS—Univ. Grenoble Alpes, Maison des Géosciences, BP 53, 38041 Grenoble Cedex 9, France
⁴Laboratoire de Chimie et Microbiologie de l’Eau, UMR CNRS 6008, Université de Poitiers, 40 avenue du recteur Pineau, 86022 Poitiers, France
⁵Conditions Extrêmes et Matériaux: Haute Température et Irradiation, UPR 3079 CNRS et université d’Orléans, 1d avenue de la recherche scientifique, 45071 Orléans Cedex 2, France
⁶Muséum National d’Histoire Naturelle, Sorbonne Universités, IMPMC UMR 7590 CNRS, 61 rue Buffon, 75005 Paris, France
Published by arrangement with John Wiley & Sons

Understanding the transformations of highly reduced enstatite chondrites (EC) in terrestrial environments, even on very short timescales, is important to make the best use of the cosmochemical and mineralogical information carried by these extraterrestrial rocks. Analogs of EC meteorites were synthesized at high pressure and high temperature. Then, their aqueous alterations, either abiotic or in the presence of the bacteria Acidithiobacillus ferrooxidans or Acidithiobacillus thiooxidans, were studied under air, at pH ~2, 20 °C, and atmospheric pressure. They stayed in shaken batch reactors for 15 days. Reference experiments were carried out separately by altering only one mineral phase among those composing the synthetic EC (i.e., sulfides: troilite or Mg‐Ca‐rich sulfides, enstatite, and Fe70Si30). Composition of the alteration aqueous media and microstructures of the weathered solids were monitored by inductively coupled plasma atomic emission spectroscopy and by scanning electron microscopy, respectively. Alteration sequence of the different mineral components of the synthetic EC was found to occur in the following order: magnesium‐calcium sulfides > troilite > iron‐silicon metallic phase > enstatite regardless of the presence or absence of the microorganisms. Such small biological effects might be due to the fact that the alteration conditions are far from biologically optimal, which is likely the case in most natural environments. The exposed surfaces of an EC meteorite falling on Earth in a wet and acidic environment could lose within a few hours their Ca‐ and Mg‐rich sulfides (oldhamite and niningerite). Then, in <1 week, troilite and kamacite could be altered. In a wet and acidic environment, only the enstatite would remain intact and would weather on a much slower geological timescale.

¹R. P. Lozano,²J. A. Sánchez,¹R. González‐Laguna,³T. Martín‐Crespo
Meteoritics & Planetary Science (in Press) Link to Article [https://doi.org/10.1111/maps.13645]
¹Museo Geominero, Instituto Geológico y Minero de España, C/Ríos Rosas 23, Madrid, 28003 Spain
²C/Rio Añamaza 4, 29620 Torremolinos, Málaga, Spain
³Departamento de Biología y Geología, Física y Química Inorgánica, ESCET, Universidad Rey Juan Carlos, C/Tulipán s/n, Móstoles, 28933 Madrid, Spain
Published by arrangement with John Wiley & Sons

Colomera is the Spanish meteorite (IIE) that has aroused the greatest interest among the international scientific community. Until now, the story of the find was only partially known and certain data are incorrect. The amazing journey of this meteorite has been recounted in this work. It reveals unpublished information derived from local archives, and testimonies from the descendants of the family that found the meteorite in 1913, and from the inhabitants of Colomera (Granada, Spain). We also document the story after its discovery, which culminated in a 2015 court ruling demanding the return of the largest part the mass (120.34 kg) to the heirs of the Spanish family that discovered the meteorite. Some of the material initially extracted in Spain (305 g) is currently housed in the Natural History Museum (121.3 g; London, UK). Nine kilograms of fragments remains in the United States after returning the meteorite to Spain in 1969. Of these, we have only located slightly more than 4 kg in several American institutions. Recently, 235 g has been returned to Spain: two fragments in private collections and two fragments in the Museo Geominero, Spanish Geological and Mining Institute (Spanish acronym: IGME).

¹Devin L.Schrader,¹Jemma Davidson,²Timothy J.McCoy,³Thomas J.Zega,⁴Sara S.Russell,³Kenneth J.Domanik,⁴Ashley J.King
Geochimica et Cosmochimica Acta (in Press) Link to Articel [https://doi.org/10.1016/j.gca.2021.03.019]
¹Center for Meteorite Studies, School of Earth and Space Exploration, Arizona State University, 781 East Terrace Road, Tempe, AZ 85287, USA
²Department of Mineral Sciences, National Museum of Natural History, Smithsonian Institution, 10th & Constitution Avenue NW, Washington, DC 20560-0119, USA
³Lunar and Planetary Laboratory, University of Arizona, Tucson, Arizona 85721, USA
⁴Planetary Materials Group, Department of Earth Sciences, Natural History Museum, Cromwell Road, London SW7 5BD, UK
Copyright Elsevier

Determining compositional trends among individual minerals is key to understanding the thermodynamic conditions under which they formed and altered, and is also essential to maximizing the scientific value of small extraterrestrial samples, including returned samples and meteorites. Here we report the chemical compositions of Fe-sulfides, focusing on the pyrrhotite-group sulfides, which are ubiquitous in chondrites and are sensitive indicators of formation and alteration conditions in the protoplanetary disk and in small Solar System bodies. Our data show that while there are trends with the at.% Fe/S ratio of pyrrhotite with thermal and aqueous alteration in some meteorite groups, there is a universal trend between the Fe/S ratio and degree of oxidation. Relatively reducing conditions led to the formation of troilite during: (1) chondrule formation in the protoplanetary disk (i.e., pristine chondrites) and (2) parent body thermal alteration (i.e., LL4 to LL6, CR1, CM, and CY chondrites). Oxidizing and sulfidizing conditions led to the formation of Fe-depleted pyrrhotite with low Fe/S ratios during: (1) aqueous alteration (i.e., CM and CI chondrites), and (2) thermal alteration (i.e., CK and R chondrites). The presence of troilite in highly aqueously altered carbonaceous chondrites (e.g., CY, CR1, and some CM chondrites) indicates they were heated after aqueous alteration. The presence of troilite, Fe-depleted pyrrhotite, or pyrite in a chondrite can provide an estimate of the oxygen and sulfur fugacities at which it was formed or altered. The data reported here can be used to estimate the oxygen fugacity of formation and potentially the aqueous and/or thermal histories of sulfides in extraterrestrial samples, including those returned by the Hayabusa2 mission and due to be returned by the OSIRIS-REx mission in the near future.

¹T.J.Barrett,¹A.Černok,¹G.Degli-Alessandrini,¹X.Zhao,^1,2M.Anand,¹I.A.Franchi,³J.R.Darling
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2021.03.018]
¹The Open University, School of Physical Sciences, Walton Hall, Milton Keynes, MK7 6AA, UK
²Department of Earth Sciences, Natural History Museum, London, SW7 5BD, UK
¹University of Portsmouth, School of the Environment, Geography and Geosciences, Burnaby Road Portsmouth, PO1 3QL, UK
Copyright Elsevier

The abundance and isotopic composition of volatile elements in meteorites is critical for understanding planetary evolution, given their importance in a variety of geochemical processes. There has been significant interest in the mineral apatite, which occurs as a minor phase in most meteorites and is known to contain appreciable amounts of volatiles (up to wt. % F, Cl, and OH). Impact-driven shock metamorphism, pervasive within many meteorites, can potentially modify the original signatures of volatiles through processes such as devolatilization and diffusion.

In this study, we investigate the microstructures of apatite grains from six eucrites across a broad range of shock stages (S1–S5) using electron backscatter diffraction (EBSD) to explore shock-induced crystallographic features in apatite. New Cl and H abundance and isotopic composition data were collected on moderate to highly shocked samples (S3-S5) by Nano Secondary Ion Mass Spectrometry (NanoSIMS). Previously reported volatile data for S1 and S2 eucrites were integrated with EBSD findings in this study.

Our findings indicate that apatite microstructures become increasingly more complex at higher shock stages. At low shock stages (S1–S2) samples display brecciation and fracturing of apatite. Samples in S3 and S4 display increasing crystal plastic deformation indicated by increasing spread in pole figures. At the higher shock stages (S4/S5) there is potential recrystallisation demonstrated by an increased density of subgrain boundaries.

The Cl content and δ37Cl values of highly-shocked apatite grains range from ∼ 940–1410 ppm and – 3.38 to + 7.70 ‰, respectively, within the range observed in less-shocked eucrites. In contrast, H2O abundances are more variable (from 186 to ∼ 4010 ppm), however, the measured water content still falls within the range previously reported for low-shock eucrites. The measured δD values range from – 157 to + 163 ‰, also within the range of values from known low-shock basaltic eucrites. Weighted averages for both isotopic systems (δD − 122 ± 20 ‰, δ37Cl + 1.76 ± 0.66 ‰) are consistent with the range displayed in other inner Solar System bodies.

NanoSIMS isotope images of apatite grains display heterogeneity in their Cl abundance at the nanoscale which increases in complexity with shock stage. This increasing complexity, however, does not correlate with deformation microstructures observed in EBSD or with the Cl isotopic composition at either an inter-grain or intra-grain scale. These findings are similar to analyses of variably shocked lunar apatite and, therefore, apatite appears to be a robust recorder of Cl and H (at least at spatial resolution and precision currently achievable by NanoSIMS) on airless bodies, despite intensive shock.

^1,2,5Derek Sears,^1,2,5Daniel Ostrowski,³Heather Smith,^1,6Adonay Sissay,⁴Mihir Trivedi
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2021.114442]
¹Arkansas Center for Space and Planetary Sciences, University of Arkansas, Fayetteville, AR 72701, USA
²BAER Institute/NASA Ames Research Center, Moffett Field, CA 94035, USA
³USRA/NASA Ames Research Center, Moffett Field, CA 94035, USA
⁴NASA Ames Research Center, Moffett Field, CA 94035, USA
⁵Department of Chemistry and Biochemistry, University of Arkansas, Fayetteville, AR 72701, USA
Copyright Elsevier

In order to find an additional quantitative way to estimate the petrographic type of unequilibrated ordinary chondrites (UOC), and one that can be used remotely in the study of asteroids, we have analyzed the near-infrared spectra of a suite of UOC observed falls. We obtained spectra from the RELAB database at Brown University and applied several methods for determining the amount of clinopyroxene (CPX) as a percentage of the total pyroxene in the meteorites. The presence of low-Ca CPX has long been known to be characteristic of little-metamorphosed ordinary chondrites. The methods we used were (1) naked-eye determination of the wavelength of the absorption features at ~1 μm and ~2 μm, (2) determination of the wavelengths of these features by fitting polynomial equations, and (3) determining the relative intensities of the CPX and OPX features after isolation by a curve fitting procedure. The measurements were then “calibrated” using data from the literature to obtain values for the amount of CPX in the total pyroxene. We find that there is an empirical relationship between the amount of CPX detected by these methods of spectrum analysis and the petrologic type.

Petrologic type = +4.402–0.019 × CPX%

We explain this empirical relationship (1) as evidence that in pyroxene bearing rocks the spectrum of pyroxene dominates (this has been known in the 1970s), (2) that low-Ca CPX is so abundant in these meteorites (up to 40 vol%) that it is easily detected by reflectance spectroscopy, and (3) compositional effects caused by Ca and Fe in the pyroxenes partially cancel out or are small. We thus have a new method of quantitatively measuring the level of metamorphic alteration experienced by these important meteorites and of assigning them a petrologic type of 3.0 to 3.9. More importantly, unlike existing methods, this can be applied remotely so that chondritic asteroid surfaces (i.e. those of Q and S asteroids) can also be characterized in terms of their metamorphic history. As an example, (433) Eros and (25143) Itokawa were found to be types ~3.5 and ~3.4, respectively. We briefly discuss the implications of this for understanding the history of meteorites and asteroids.

¹Maxime Piralla,²Romain Tartèse,¹Yves Marrocchi,²Katherine H. Joy
Meteoritics & Planetary Science (in Press) Link to Article [https://doi.org/10.1111/maps.13639]
¹CRPG, CNRS, UMR 7358, Université de Lorraine, Vandœuvre‐lès‐Nancy, F‐54500 France
²Department of Earth and Environmental Sciences, School of Natural Sciences, The University of Manchester, Oxford Road, Manchester, M13 9PL UK
Published by arrangement with John Wiley & Sons

Apatite has been widely used for assessing the volatile inventory and hydrothermal fluid compositions of asteroidal and planetary bodies. We report the OH, F, and Cl abundances, as well as the hydrogen isotope composition, of apatite in the CM1‐2 chondrite Boriskino and in the C1‐ungrouped Bench Crater meteorite. Apatite in both meteorites is halogen‐poor, close to the hydroxylapatite endmember composition, and characterized by average δDSMOW values of −226 ± 59% and 233 ± 92%, respectively. Compared to apatite, the matrix in Bench Crater is depleted in D with a δDSMOW value of −16 ± 119‰. Comparing apatite and water H isotope compositions yields similar apatite‐water D/H fractionation ΔDApatite‐Water of approximately 120–150‰ for both chondrites, suggesting that apatite formed at similar temperatures. Combining a lattice strain partitioning model with apatite F and Cl abundances in Boriskino and Bench Crater yields low F and Cl abundances <300 μg g−1 in apatite‐forming fluids, and fluid F/Cl ratios that are roughly consistent with the bulk F/Cl ratios of other CI and CM chondrites. This suggests that hydrothermal alteration on these meteorite parent bodies took place under closed‐system conditions. Based on the OH abundance estimates for the apatite‐forming fluids, we estimated the pH values of alteration fluids to be of approximately 10–13. Such alkaline fluid compositions are consistent with previous modeling and suggest that apatite formed late, toward the end of completion of hydrothermal alteration processes on the Boriskino and Bench Crater parent bodies.