Light noble gases in 11 achondrites: Cosmic ray exposure ages, gas retention ages, and preatmospheric sizes

1Thomas Smith,1,2,3Huaiyu He,4Shijie Li,1Fei Su
Meteoritics & Planetary Science (in Press) Link to Article [https://doi.org/10.1111/maps.14085]
1State Key Laboratory of Lithospheric Evolution, Institute of Geology and Geophysics, Chinese Academy of Sciences, Beijing, China
2Institutions of Earth Science, Chinese Academy of Sciences, Beijing, China
3College of Earth and Planetary Sciences, University of Chinese Academy of Sciences, Beijing, China
4Center for Lunar and Planetary Sciences, Institute of Geochemistry, Chinese Academy of Sciences, Guiyang, China
Published by arrangement with John Wiley & Sons

We report light noble gas (He, Ne, and Ar) concentrations and isotopic ratios in 11 achondrites, Tafassasset (unclassified primitive achondrite), Northwest Africa (NWA) 12934 (angrite), NWA 12573 (brachinite), Jiddat al Harasis (JaH) 809 (ureilite), NWA 11562 (ungrouped achondrite), four lodranites (NWA 11901, NWA 7474, NWA 6685, and NWA 6484), NWA 2871 (acapulcoite), and Sahara 02029 (winonaite), most of which have not been previously studied for noble gases. We discuss their noble gas isotopic composition, determine their cosmogenic nuclide content, and systematically calculate their cosmic ray exposure (CRE) and gas retention ages. In addition, we estimate their preatmospheric radii and preatmospheric masses based on the shielding parameter (22Ne/21Ne)cos. None of the studied meteorites shows evidence of contribution from solar cosmic rays (SCRs). JaH 809 and NWA 12934 show evidence of 3He diffusive losses of >90% and 40%, respectively. The winonaite Sahara 02029 has lost most of its noble gases, either during or before analysis. The average CRE age of Tafassasset of ~49 Ma is lower than that reported by Patzer et al. (2003), but is consistent with it within the uncertainties; this confirms that Tafassasset and CR chondrites are not source paired, CR chondrites having CRE ages from 1 to 25 Ma (Herzog & Caffee, 2014). The ureilite JaH 809 has a CRE age of ~5.4 Ma, which falls into the typical range of exposure ages for ureilites; the angrite NWA 12934 has a CRE age of ~49 Ma, which is within the main range of exposure ages reported for angrites (0.2–56 Ma). We calculate a CRE age of ~2.4 Ma for the brachinite NWA 12573, which falls into a possible “cluster” in the brachinite CRE age histogram around ~3 Ma. Three lodranites (NWA 11901, NWA 7474, and NWA 6685) have CRE ages higher than the average CRE ages of lodranites measured so far, NWA 11901 and NWA 6685 having CRE ages far higher than the CRE age already reported by Li et al. (2019) on NWA 8118. The measured 40K-40Ar gas retention ages fit well into established systematics. The gas retention age of Tafassasset is consistent, within respective uncertainties, with that previously calculated by Patzer et al. (2003). Our study indicates that Tafassasset originates from a meteoroid with a preatmospheric radius of ~20 cm, however discordant with the radius of ~85 cm inferred in a previous study (Patzer et al., 2003).

The “Meteorite meter”: A handheld instrument for the combined measurement of magnetic susceptibility and electrical conductivity, with application to meteorite identification and classification

1Minoru Uehara,1Jérôme Gattacceca
Meteoritics & Planetary Science (in Press) Open Access Link to Article [https://doi.org/10.1111/maps.14087]
1CNRS, IRD, INRAE, CEREGE, Aix Marseille Univ, Aix-en-Provence, France
Published by arrangement with John Wiley & Sons

We developed a simple, handheld, and user-friendly magnetic susceptibility meter specialized for the identification of meteorites. The measurement is based on an LC resonance circuit. When provided with a rough estimate of the sample mass, the instrument displays directly the mass-normalized magnetic susceptibility expressed in logχm (with χm in 10−9 m3 kg−1), a parameter that is widely used in the classification of meteorites. Moreover, the measurement of the impedance of the LC resonator provides a proxy of the electrical conductivity (C-index) that can be helpful to distinguish metal-bearing samples from magnetite-bearing samples. This C-index offers an additional diagnostic for the identification of meteorites. Our tests demonstrate that the precision and the accuracy of this instrument called “Meteorite meter” (MetMet) are sufficient to allow distinguishing most meteorites from most terrestrial rocks, for a minimum recommended sample mass of 5 g. The distinction of some meteorite groups is also possible, in particular the separation of the three ordinary chondrite groups. Meteorite hunters, collectors, and curators and non-specialists, including children, can use this instrument as a guidance in the identification and classification of meteorites. This kind of instrument has an immense advantage over the widely used testing of meteorites with magnets, as it does not affect the paleomagnetic records of meteorites that are highly valuable for scientists.

Pyroxene and Hydroxyl Signatures in Vesta Newly Calibrated Data from Dawn Mission

1,2Massa, Giuseppe,2Longobardo, Andrea,2Palomba, Ernesto,1,2Angrisani, Marianna,1,2Gisellu, Chiara,Dirri, Fabrizio,2De Sanctis, Maria Cristina,2Raponi, Andrea,2Carrozzo, Filippo Giacomo,2Ciarniello, Mauro
Universe 9, 296 Open Access Link to Article [DOI 10.3390/universe9060296]
1INAF Istituto di Astrofisica e Planetologia Spaziali, Rome, 00133, Italy
2Department of Information Engineering, Electronics and Telecommunications, University of Rome “Sapienza”, Rome, 00185, Italy

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Abundant extraterrestrial purine nucleobases in the Murchison meteorite: Implications for a unified mechanism for purine synthesis in carbonaceous chondrite parent bodies

1Toshiki Koga,1Yoshinori Takano,2Yasuhiro Oba,3Hiroshi Naraoka,1Naohiko Ohkouchi
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2023.10.024]
1Biogeochemistry Research Center (BGC), Japan Agency for Marine-Earth Science and Technology (JAMSTEC), 2-15 Natsushima, Yokosuka, Kanagawa 237-0061, Japan
2Institute of Low Temperature Science (ILTS), Hokkaido University, N19W8, Kita-ku, Sapporo, Hokkaido 060-0189, Japan
3Department of Earth and Planetary Sciences, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka, Fukuoka, 819-0395, Japan
Copyright Elsevier

Extraterrestrial nucleobases are of key interest owing to their implications for the chemical evolution of primordial molecules in the solar system and their potential contributions to prebiotic chemistry on the early Earth. Recent advances in analytical techniques capable of detecting femto-mole-order nucleobases have allowed us to identify all five exogenous nucleobases—uracil, cytosine, thymine, adenine, and guanine—in carbonaceous chondrites and to quantify uracil obtained from the carbonaceous asteroid (162173) Ryugu. In this study, we optimized the analytical method using hot-water extraction followed by 6 M hydrochloric acid (HCl) extraction from a sample of the CM2 Murchison meteorite to reassess the abundances and distributions of extraterrestrial nucleobases. The target analyses performed using high-performance liquid chromatography paired with electrospray-ionization, high-resolution mass spectrometry revealed that purine nucleobases were substantially more enriched in the subsequent 6 M HCl extract (951 ± 104 parts per billion, ppb) than in the hot-water extract (199 ± 3 ppb). The most abundant nucleobase was guanine (649 ± 103 ppb in total). The 6 M HCl extract not only contained canonical nucleobases but also included rare nucleobase analogs from the purine family, such as 8-substituted purines. Unlike purines, we preferentially detected pyrimidine nucleobases in the hot-water extract and the acid hydrolysate (185 ± 17 ppb and 297 ± 5 ppb, respectively) rather than in the 6 M HCl extract (51 ± 4 ppb). The disparate distributions of purine and pyrimidine bases in the Murchison meteorite suggests that purines are more robustly incorporated than pyrimidines into meteoritic matrices and/or insoluble macromolecular organic matter. We propose a unified formation mechanism for purine nucleobases—which involves the synthesis of 5-aminoimidazole derivatives from hydrogen cyanide and its related molecules—that can account for the molecular distributions of the extraterrestrial purine nucleobases found in the Murchison meteorite.

Physical properties and average atomic numbers of chondrules using computed tomography

1,2Yogita Kadlag,3David Haberthür,2Ingo Leya,3Ruslan Hlushchuk,4Klaus Mezger
Planetary and Space Science (in Press) Link to Article [https://doi.org/10.1016/j.pss.2023.105799]
1Geosciences Division, Physical Research Laboratory, Navrangpura, 380009, Ahmedabad, India
2Space Science and Planetology, Physikalisches Institut, Universität Bern, Sidlerstrasse 5, 3012, Bern, Switzerland
3Institut für Anatomie, Universität Bern, Baltzerstrasse 2, 3012, Bern, Switzerland
4Institut für Geologie, Universität Bern, Baltzerstrasse 1+3, 3012, Bern, Switzerland

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Detectability of carbon with ChemCam LIBS: Distinguishing sample from Mars atmospheric carbon, and application to Gale crater

1P.Beck et al. (>10)
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2023.115840]
1Univ. Grenoble Alpes, IPAG, F-38000 Grenoble, France
Copyright Elsevier

Onboard NASA’s Curiosity rover, the ChemCam LIBS instrument has provided a wealth of information on the chemistry of rocks within Gale crater. Here, we use ChemCam in order to search for carbonates among the >3500 individual targets analyzed by this instrument. Because the carbon-lines are a combination of signal from the CO2-rich atmosphere and possible carbon from the targets, we developed a laboratory-based univariate calibration obtained under Mars-like atmosphere. We measured different type of carbon-bearing samples (sediments, coals, carbonates) and their mixture with a basaltic powder. Based on this work, the preferred approach to qualitatively assess carbon under a CO2-rich atmosphere is to use a ratio to an oxygen line (777 nm) and the estimated limit of detection for carbon in a single LIBS point are found to be of 4.5 wt% and 6.9 wt% for reduced and organic carbon, respectively. Considering carbonate, this LOD correspond to about 50 wt% carbonate in the analyzed volume.

Analysis of data obtained on Mars by ChemCam up to sol 3350 reveals the presence of a correlation between the intensity of carbon and oxygen lines, as observed in the laboratory, confirming that most carbon signal is related to ionization of the atmosphere. Some variability in the carbon signal appears related to the physical state of the atmosphere (density, temperature).

Based on a combined analysis of carbon lines and major element compositions (Ca, Fe, Mg), there was no detection of carbonate in the ChemCam dataset up to sol 3355. Therefore, we conclude that carbonate was not present as a major constituent (>50%) in the ChemCam LIBS targets, and that soils are not enriched in carbon beyond the limit of detection. The dominant salts present are sulfate, chlorides, and the lack of carbonates in Gale, while observed in Jezero, may at least partly be related to a difference in protolith.

Volatiles, vesicles, and vugs: Unraveling the magmatic and eruptive histories of Steno crater basalts

1Z.E. Wilbur et al.(>10)
Meteoritics & Planetary Science (in Press) Open Access Link to Article [https://doi.org/10.1111/maps.14086]
1Lunar and Planetary Laboratory, University of Arizona, Tucson, Arizona, USA
Published by arrangement with John Wiley & Sons

In 1972, Apollo 17 astronauts returned 170.4 kg of lunar material. Within 1 month of their return, a subset of those samples was specially curated with the forethought that future analytical techniques would offer new insight into the formation and evolution of the Moon. Of interest in this work is sample 71036, a basalt collected from the rim of Steno crater in the Taurus–Littrow Valley, which was stored frozen and was processed and released for study 50 years later. We report, for the first time, the detailed mineralogy and petrology of 71036 and its companion samples 71035, 71037, and 71055 using a novel combination of 2-D and 3-D methods. We investigate lunar volatiles through in situ measurements of apatite and 3-D measurements of vesicles to understand the degassing histories of the Steno crater basalts. Our coupled 2-D petrography and 3-D tomography data sets support a model of the Steno crater basalts crystallizing in the upper crust of a mare lava flow. Apatite F and OH chemistry and the late-stage deformation of voids and formation of smaller vesicles provide evidence supporting coeval degassing of volatiles and crystallization of mesostasis apatite in Apollo 17 basalts. This work helps to close knowledge gaps surrounding the origin, magmatic evolution, emplacement, and crystallization history of high-titanium basalts.

Evaporation of moderately volatile elements from metal and sulfide melts: Implications for volatile element abundances in magmatic iron meteorites

1E.S. Steenstra,1C.J. Renggli,1J. Berndt,1S. Klemme
Earth and Planetary Science Letters 622, 118406 Link to Article [https://doi.org/10.1016/j.epsl.2023.118406]
1Institute of Mineralogy, University of Münster, Germany
Copyright Elsevier

Volatile element abundances in magmatic iron meteorites provide fundamental insights into the processing of volatile elements in the early solar system. Although Cu, Ge and Ag concentrations of magmatic iron meteorites deviate up to 4 orders of magnitude between different magmatic iron meteorite groups, the role of evaporation on these volatile abundances is poorly constrained. Here, we experimentally assess the volatility of Cu, Ge, Ag, S, Cr, Co, Ni, Mo, Ru, Pd, W, Re and Ir from metal and sulfide melts as a function of pressure (10−4 and 1 bar), temperature (1573–1823 K) and time (5–120 min) for two end-member compositions (Fe versus FeS). These novel experiments demonstrate that the presence of S is a major parameter in establishing the volatility of Cu, Ge, Mo, Ag, Ru, W, Re and Ir. At constant P-T and time, the volatility of Ge, Mo, Ru, W, Re and Ir is greatly increased in the presence of S, whereas Cu and Ag are less volatile in the presence of S. At 1773 K and ∼0.001 bar, the volatility of S is sufficiently high that the degassed FeS liquid showed immiscibility of a S-rich sulfide and a S-poor Fe melt. Empirical equations were derived that predict the evaporative loss of Cu, Ge, Mo, Ag from Fe and/or FeS liquid as a function of temperature and time. A comparison of the newly derived volatility sequences with commonly applied 50% condensation temperature models shows that the condensation temperature models cannot be applied to sulfur-bearing Fe liquids and therefore to magmatic iron meteorites. Application of the new models on previously derived elemental depletions in the IVB parent body shows that evaporation, if it occurred, cannot have taken place under S-rich conditions. The latter would result in a depletion of Mo, which is not observed for the IVB irons. However, evaporation of a S-free or S-poor Fe liquid reproduces the observed volatility depletion trend for IVB irons under a wider range of temperature and evaporation times, demonstrating the potential importance of evaporative loss on the IVB parent body.

Magnetic Recording Stability of Taenite-Containing Meteorites

1Devienne, José A. P. M.,1Berndt, Thomas A.,2Williams, Wyn, 3Nagy, Lesleis
Geophysical Research Letters 50, e2022GL102602 Open Access Link to Article [DOI 10.1016/j.jas.2023.105827]
1Department of Geophysics, School of Earth and Space Sciences, Peking University, Beijing, China
2School of GeoSciences, The University of Edinburgh, Edinburgh, United Kingdom
3Department of Geophysics, Ocean and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom

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An arrowhead made of meteoritic iron from the late Bronze Age settlement of Mörigen, Switzerland and its possible source

1,2Hofmann, B.A. et al. (>10)
Journal of Archaelogical Research 157, 105827 Link to Article [DOI 10.1016/j.jas.2023.105827]
1Naturhistorisches Museum Bern, Bernastrasse 15, Bern, CH-3005, Switzerland
2Institute of Geological Sciences, University of Bern, Baltzerstrasse 1+3, Bern, CH-3012, Switzerland

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