Effects of hot desert weathering on highly siderophile elements in ordinary chondrites

1Kiran Shahood Almas,1Richard D. Ash,1Richard J. Walker
Meteoritics & Planetary Science (in Press) Open Access Link to Article [https://doi.org/10.1111/maps.14267]
1Department of Geology, University of Maryland, College Park, Maryland, USA
Published by arrangenent with John Wiley & Sons

Over 20,000 meteorites have been recovered from hot deserts. The effects of hot desert weathering upon highly siderophile elements (HSE) have been little studied. We have investigated the effects of neutral to mildly acidic leaching of three L6-type ordinary chondrites of different weathering grades on HSE concentrations and Re-Os isotopic systematics. We have characterized the bulk sample HSE patterns of these meteorites and conducted leaching experiments with progressively longer leaching times to determine the possible effects of long-term residence in a desert. The most weathered sample (NWA 14239) displayed greater HSE concentration homogeneity than the other samples and released lower quantities of HSEs during leaching. Water leaching was milder than acetic acid and did not significantly modify the Re-Os isotopic systematics of the residue relative to the bulk sample of NWA 869. Short-term leachates of the less weathered samples (Viñales and NWA 869) were characterized by low 187Os/188Os ratios, indicating the preferential dissolution of early solar system–formed phases such as non-magnetic chondrules and matrix with low Re/Os that are no longer intact in the most weathered sample. Of the HSE, Pd is most resistant to both water and acetic acid leaching, with a maximum removal of ~5% Pd, while Re, Os, and Ir are most mobile with up to 40% removal.

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

1,2Mingbao Li,3,4Ke Zhu,1,5Yan Fan,6P. M. Ranjith,7Chao Wang,1Wen Yu, 1,8,9Shijie Li
The Planetary Science Journal 5, 178 Open Access Link to Article [DOI 10.3847/PSJ/ad6154]
1Center for Lunar and Planetary Sciences, Institute of Geochemistry, Chinese Academy of Sciences, Guiyang 55021, People’s Republic of China
2State Key Laboratory of Lunar and Planetary Sciences, Macau University of Science and Technology, Macau 999078, People’s Republic of China
3Freie Universität Berlin, Institut für Geologische Wissenschaften, Malteserstr. 74-100, Berlin 12249, Germany
4Bristol Isotope Group, School of Earth Sciences, University of Bristol, Wills Memorial Building, Queen’s Road, Bristol BS8 1RJ, UK
5State Key Laboratory of Continental Dynamics and Department of Geology, Northwest University, Xi’an 710069, People’s Republic of China
6Graduate School of Advanced Science and Technology, Japan Advanced Institute of Science and Technology (JAIST), 1-1 Asahidai, Nomi, Ishikawa, 923-1292, Japan
7School of Earth and Space Sciences, Peking University, Beijing 100871, People’s Republic of China
8CAS Center for Excellence in Comparative Planetology, Hefei, 230022, People’s Republic of China

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Low temperature phase transitions in the visible and near-infrared (VNIR) reflectance spectra of (NH4)2HPO4 and (NH4)HSO4 salts

1M. Fastelli, 2B. Schmitt, 2P. Beck, 2O. Poch, 1A. Zucchini, 1P. Comodi
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2024.116321]
1Department of Physics and Geology, University of Perugia, I-06123 Perugia, Italy
2Univ. Grenoble Alpes, CNRS, IPAG, 38000 Grenoble, France
Copyright Elsevier

The detection of ammonium bearing crystalline solids in salt-water systems on icy bodies and solar system bodies could provide information about the ascent of these salts from a deep reservoir within the hydrosphere. Due to their chemical-physical properties, NH4+ compounds play a key role both in the internal dynamics of celestial bodies and in the potential habitability of ocean worlds.. In this work we analysed the reflectance spectra of two synthetic NH4+ salts: ammonium hydrogen phosphate (NH4)2HPO4 and ammonium hydrogen sulphate (NH4)HSO4 in the 1–4.2 μm spectral range at low temperature, between 110 and 290 K. For (NH4)2HPO4 we also examined the effect of three different grain sizes (150–125 μm; 125–80 μm; 80–32 μm). The collected reflectance spectra show absorption features related to NH4+ group overtone and combination modes in the 1–2.5 μm range. In particular, the bands located at ~1.09 μm (3ν3), ~1.30 μm (2ν3 + ν4), ~1.58 μm (2ν3), ~2.02 μm (ν2 + v3) and ~ 2.2 μm (v3 + v4) could be useful to discriminate these salts. The low temperature spectra, compared to those at ambient temperature, reveal finer structures, displaying sharper and narrower absorption bands. The selected NH4+-bearing salts are subjected to reversible low temperature phase transitions, which are revealed in the spectra by a progressive growth and shift of the bands toward shorter wavelengths with a drastic change of their depth. We performed laboratory measurements ammonium (NH4+) compounds to address the limited data available expanding the existing database. The collected cryogenic spectra can be directly compared with remote sensing data from planetary missions of the upcoming decade such as NASA’s Europa Clipper, and ESA’s JUICE and the newly launched James Webb Space Telescope expanding the existing database of ammonium compounds at cryogenic temperature.

Fe, Zn, and Mg stable isotope systematics of acapulcoite lodranite clan meteorites

1,2Stepan M. Chernonozhkin,3Lidia Pittarello,4Genevieve Hublet,5Philippe Claeys,4Vinciane Debaille,1Frank Vanhaecke,5Steven Goderis
Meteoritics & Planetary Science (in Press) Open Access Link to Article [https://doi.org/10.1111/maps.14258]
1Atomic & Mass Spectrometry—A&MS Research Unit, Department of Chemistry, Ghent University, Ghent, Belgium
2Isotope Ratio Analysis Research Group, Chair of General and Analytical Chemistry, Montanuniversität Leoben, Leoben, Austria
3Naturhistorisches Museum Wien – NHMW, Vienna, Austria
4Laboratoire G-Time, Université Libre de Bruxelles, Brussels, Belgium
5Archaeology, Environmental Changes, and Geo-Chemistry (AMGC), Vrije Universiteit Brussel, Brussels, Belgium
Published by arrangement with John Wiley & Sons

The processes of planetary accretion and differentiation, whereby an unsorted mass of primitive solar system material evolves into a body composed of a silicate mantle and metallic core, remain poorly understood. Mass-dependent variations of the isotope ratios of non-traditional stable isotope systems in meteorites are known to record events in the nebula and planetary evolution processes. Partial melting and melt separation, evaporation and condensation, diffusion, and thermal equilibration between minerals at the parent body (PB) scale can be recorded in the isotopic signatures of meteorites. In this context, the acapulcoite–lodranite meteorite clan (ALC), which represents the products of thermal metamorphism and low-degree partial melting of a primitive asteroid, is an attractive target to study the processes of early planetary differentiation. Here, we present a comprehensive data set of mass-dependent Fe, Zn, and Mg isotope ratio variations in bulk ALC species, their separated silicate and metal phases, and in handpicked mineral fractions. These non-traditional stable isotope ratios are governed by mass-dependent isotope fractionation and provide a state-of-the-art perspective on the evolution of the ALC PB, which is complementary to interpretations based on the petrology, trace element composition, and isotope geochemistry of the ALC. None of the isotopic signatures of ALC species show convincing co-variation with the oxygen isotope ratios, which are considered to record nebular processes occurring prior to the PB formation. Iron isotopic compositions of ALC metal and silicate phases broadly fall on the isotherms within the temperature ranges predicted by pyroxene thermometry. The isotope ratios of Mg in ALC meteorites and their silicate minerals are within the range of chondritic meteorites, with only accessory spinel group minerals having significantly different compositions. Overall, the Mg and Fe isotopic signatures of the ALC species analyzed are in line with their formation as products of high-degree thermal metamorphism and low-degree partial melting of primitive precursors. The δ66/64Zn values of the ALC meteorites demonstrate a range of ~3.5‰ and the Zn is overall isotopically heavier than in chondrites. The superchondritic Zn isotopic signatures have possibly resulted from evaporative Zn losses, as observed for other meteorite parent bodies. This is unlikely to be the result of PB differentiation processes, as the Zn isotope ratio data show no covariation with the proxies of partial melting, such as the mass fractions of the platinum group and rare earth elements.

On the origin and evolution of deuterium enrichment in type 1 and 2 chondritic organic solids

1George D. Cody, 1Conel M. O’D. Alexander, 1Dionysis I. Foustoukos, 1,2Yoko Kebukawa, 1Ying Wang
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2024.09.023]
1Earth and Planets Laboratory, Carnegie Institution for Science, 5241 Broad Branch Road, NW, Washington, DC, United States
2Tokyo Institute of Technology, Department of Earth and Planetary Science, Tokyo, Japan
Copyright Elsevier

Rotationally resonant Deuterium Nuclear Magnetic Resonance spectroscopy (D MAS NMR) was applied to IOM isolated from a CR1 chondrite Grosvenor Mountains (GRO) 95577 and a CM2 chondrite (Murchison). It is shown that in IOM D strongly prefers the aliphatic hydrogen reservoir over the aromatic hydrogen reservoir. For GRO 95577, that has a bulk δD of 3303 ‰ (Alexander et al., 2010), the average δD value of the aromatic reservoir is 1740 ± 128 ‰ and the aliphatic reservoir is 4477 ± 105 ‰, i.e., D/H enrichments of 1.27 and 0.64, respectively, relative to the bulk. For Murchison IOM, that has a bulk δD of 811 ‰ (Alexander et al., 2010), the average δD of the aromatic reservoir is 512 ± 88 ‰ and the aliphatic reservoir is 1033 ± 64 ‰ i.e., D/H enrichments of 1.12 and 0.82, respectively, relative to the bulk. D-H exchange between D-enriched water and a type III kerogen reveals nearly equivalent D up take by both aromatics and aliphatics. Laboratory synthesis of IOM-like material in the presence of D2O reveals a high degree of deuteration with a strong preferential deuteration of the aliphatic hydrogen reservoir indicating that the δD of the water during IOM synthesis is the primary determinant of syn-IOM’s δD. The IOM in GRO 95577 and Murchison (FA and H/C × 100) lie on the molecular evolution line as defined by the IOM of the Tagish Lake clasts and Murchison IOM has experienced more molecular evolution relative to that exhibited by GRO 95577 IOM. A forward prediction derived from the D/H ratios for the aliphatic and aromatic hydrogen reservoirs in Murchison and GRO 95577, relative to their bulk D/H ratios, derived from D MAS NMR, is applied to explain the origin of the Tagish Lake trend of δD vs molecular evolution (H/C × 100). The results of this forward prediction suggest that the Tagish Lake isotopic trend results from a combination of molecular evolution (loss of predominantly aliphatic H and D) and partial D-H exchange with D depleted chondritic water during a short-term hydrothermal alteration event. Such events may be faithfully identified in chondritic organic solids and be a common occurrence, but not necessarily revealed in the mineralogy of type 1 and 2 carbonaceous chondrites.

Early generation of a refractory inclusions-enriched H-chondritic parent body: A safe harbor for Ca, Al-rich inclusions

1Samuel Ebert, 2Kazuhide Nagashima, 2Alexander N. Krot, 3Shigeru Wakita, 4Jean-Alix Barrat, 1Addi Bischoff
Earth and Planetary Science Letters 646, 119010, Open Access Link to Article [https://doi.org/10.1016/j.epsl.2024.119010]
1Institut für Planetologie, University of Münster, D-48149, Münster, Germany
2Hawai‘i Institute of Geophysics and Planetology, University of Hawai‘i at Mānoa, Honolulu, HI 96822, USA
3Department of Earth, Atmospheric, and Planetary Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA
4Institut Universitaire Européen de la Mer, Université de Bretagne Occidentale, Place Nicolas Copernic, F-29280, Plouzané Cedex, France
Copyright Elsevier

Calcium-aluminum-rich inclusions (CAIs) commonly observed in chondritic meteorites are the oldest dated solids formed in the Solar System. Short-lived isotope chronologies (26Al-26Mg, 182Hf-182W) suggest a ∼2 Ma gap between the formation of CAIs and the accretion of the final chondrite parent bodies. One thin section, 3.27 cm2 in size, of an ordinary chondrite NWA 3358 (H3.1) studied contains 52 refractory inclusions (CAIs and amoeboid olivine aggregates (AOAs)) comprising 0.14 % of its area, which is the highest abundance of refractory inclusions among non-carbonaceous chondrites containing on average ∼0.009 area % of CAIs and AOAs. In combination with a low chondrule/matrix ratio of ∼1.5, this makes NWA 3358 a unique ordinary chondrite. The aqueously-formed fayalites (Fa>99) in NWA 3358 have the inferred initial 53Mn/55Mn ratio of (5.56 ± 0.44) × 10−6 which is the highest measured value for secondary minerals in chondrites and corresponds to the formation time of ∼1.0–1.5 Ma after CAIs. Based on the 53Mn-53Cr chronology of fayalite formation and the thermal modeling, we infer that the first-generation of an H chondrite parent body, ∼6–12 km in diameter, accreted within 1.0 Ma after formation of CAIs, filling the gap of ∼2 Ma between CAIs and the earliest chondrite parent bodies. This early accretion provides a possible mechanism of CAIs/AOAs storage in the inner solar nebula and could explain the high amount of refractory inclusions in NWA 3358. A later destruction of these first-generation bodies may also explain the presence of CAIs and chondrules of different ages within later formed chondrite parent bodies.

The very late-stage crystallization of the lunar magma ocean and the composition of immiscible urKREEP

1,2Yishen Zhang, 3,4,5Bernard Charlier, 4Stephanie B. Krein, 4Timothy L. Grove, 1,5Olivier Namur, 5Francois Holtz
Earth and Planetary Science Letters 646, 118989 Link to Article [https://doi.org/10.1016/j.epsl.2024.118989]
1Department of Earth and Environmental Sciences, KU Leuven, 3001 Leuven, Belgium
2Department of Earth, Environmental and Planetary Sciences, Rice University, 6100 Main Street, MS 126, Houston, TX 77005, USA
3Department of Geology, University of Liège, 4000 Sart Tilman, Belgium
4Massachusetts Institute of Technology, Department of Earth, Atmospheric, and Planetary Sciences, Cambridge, MA 02139 USA
5Institut für Erdsystemwissenschaften, IESW, Abteilung Mineralogie, Leibniz Universität Hannover, 30167 Hannover, Germany
Copyright Elsevier

The latest stages of the lunar magma ocean (LMO) crystallization led to the formation of ilmenite-bearing cumulates and urKREEP, residual melts enriched in K, rare earth elements (REEs), P, and other incompatible elements. Those highly evolved lithologies had major impacts on the petrogenesis of lunar volcanic rocks and the compositional diversity of post-LMO magmatism resulting from mantle remelting. Here, we present new experimental results constraining the composition of the very last liquids produced during LMO crystallization. To test the potential role of silicate liquid immiscibility in the formation of urKREEP, synthetic samples representative of residual melts of bulk Moon compositions were placed in double platinum-graphite capsules at 1020–980 °C and 0.08–0.10 GPa in an internally-heated pressure vessel. The produced silicate liquids are multiply saturated with plagioclase, augite, silica phases, and ilmenite (± fayalitic olivine ± pigeonite). Our experiments show that the liquid line of descent reaches a two-liquid field at 1000 °C and >97% crystallization for a range of whole-Moon compositions. Under these conditions, a small proportion of silica-rich melt (70.0–71.4 wt.% SiO2, 6.4–7.3 wt.% FeO, 5.4–6.1 wt.% K2O, 0.2–0.3 wt.% P2O5) coexists within an abundant Fe-rich melt (42.6–44.1 wt.% SiO2, 27.6–28.8 wt.% FeO, 0.9–1.0 wt.% K2O, 2.8–3.2 wt.% P2O5) with sharp two-liquid interfaces. Our experimental results also constrain the relative onset of ilmenite crystallization compared to the development of immiscibility and indicate that an ilmenite-bearing layer formed in the lunar interior before immiscibility was attained. Using a self-consistent physicochemical LMO model, we constrain the thickness and depth of the ilmenite-bearing layer during LMO differentiation. The immiscible K-Si-rich and P-Fe-rich melts together also produced an immiscible urKREEP layer ∼2–6 km thick and ∼30–50 km deep depending on the trapped liquid fraction in the cumulate column (≤10%) and the thickness of the buoyant anorthosite crust (30–50 km). We provide constraints on the relationship between the compositions of immiscible urKREEP melts and those of KREEPy rocks. By modeling the mixing of KREEP-poor basalt and the immiscible melt pairs, we reproduce the K and P enrichments and apparent decoupling of K from P in KREEPy rocks. Our results highlight that processes such as the assimilation of evolved heterogeneous mantle lithologies may be involved in hybridization during post-LMO magmatism. The immiscible K-Si-rich lithology may also have contributed to lunar silicic magmatism.

Evidence suggesting that earth had a ring in the Ordovician

1Andrew G. Tomkins, 1Erin L. Martin, 1Peter A. Cawood
Earth and Planetary Science Letters 646, 118991 Open Access Link to Article [https://doi.org/10.1016/j.epsl.2024.118991]
1School of Earth, Atmosphere and Environment, Monash University, Melbourne, Victoria 3800, Australia
Copyright Elsevier

All large planets in our Solar System have rings, and it has been suggested that Mars may have had a ring in the past. This raises the question of whether Earth also had a ring in the past. Here, we examine the paleolatitudes of 21 asteroid impact craters from an anomalous ∼40 m.y. period of enhanced meteor impact cratering known as the Ordovician impact spike, and find that all craters fall in an equatorial band at ≤30°, despite ∼70 % of exposed, potentially crater-preserving crust lying outside this band. The beginning of this period is marked by a large increase in L chondrite material accumulated in sedimentary rocks at 465.76 ± 0.30 Ma, which, together with the impact spike, has long been suggested to result from break-up of the L chondrite parent body in the asteroid belt. Our binomial probability calculation indicates that it is highly unlikely that the observed crater distribution was produced by bolides on orbits directly from the asteroid belt (P = 4 × 10–8). We therefore propose that instead, a large fragment of the L chondrite parent body broke up due to tidal forces during a near-miss encounter with the Earth at ∼466 Ma. Given the longevity of the impact spike and sediment-hosted L chondrite debris accumulation, we suggest that a debris ring formed after this break up event, from which material deorbited to produce the observed crater distribution. We further speculate that shading of Earth by this ring may have triggered cooling into the Hirnantian global icehouse period.