Evidence for Very Early Planetesimal Formation and 26Al/27Al Heterogeneity in the Protoplanetary Disk

1J. N. Connelly,1J. Bollard,1E. Amsellem,1M. Schiller,1K. K. Larsen,1M. Bizzarro
The Astrophysical Journal Letters 952, L33 Open Access Link to Article [DOI 10.3847/2041-8213/ace42e]
1Centre for Star and Planet Formation, Globe Institute, University of Copenhagen, Øster Voldgade 5–7, DK-1350, Copenhagen, Denmark; connelly@sund.ku.dk

We present a U-corrected Pb–Pb age of 4566.19 ± 0.20 Ma (1.11 ± 0.26 Myr after t0) for the moderately volatile element rich, andesitic meteorite Erg Chech 002 (EC002). Our Al–Mg isochron defines a 26Al/27Al initial ratio of (8.65 ± 0.09) × 10−6 that corresponds to a 26Al/27Al ratio of 2.48−0.56+0.67 × 10−5 for the parent body precursor at the time of solar system formation. Whereas the published bulk chemistry and our high-precision Ca isotope measurement correspond to those for inner solar system materials, the 26Al/27Al ratio overlaps that for outer solar system CI chondrites. This indicates that the carriers and/or processes responsible for the nucleosynthetic isotope compositions for inner and outer disk materials are different than those controlling the heterogeneous distribution of 26Al. A low μ26Mg* initial value of −6.1 ± 1.7 ppm infers a source region with a subchondritic Al/Mg ratio until 1.1 Myr after t0 such that melt generation must have immediately preceded its crystallization. With 26Al as the main heating source, a modeled temperature–time path for a 100 km radius parent body with our inferred 26Al abundance suggests that accretion must have occurred before 0.5 Myr after t0 to reach melting temperatures at appropriate depths within 1.1 Myr. This requires that the parent body formed very early within the protoplanetary disk, consistent with predictions of rapid formation of planetesimals by streaming instabilities within high-density dust filaments during the earliest phase of the protoplanetary disk. Finally, an absence of initial Pb in this otherwise moderately volatile-rich achondrite implies Pb was effectively sequestered to the Fe–Ni core.

Mechanochemical Synthesis of Amorphous Silicates with an Enstatite and Forsterite Composition

1C. Koike, 1H. Chihara
The Astrophysical Journal 951, 24 Open Access Link to Article [DOI 10.3847/1538-4357/acd002]
1Department of Environmental Science and Technology, Faculty of Design Technology, Osaka Sangyo University, 3-1-1 Nakagaito, Daito, Osaka 574-8530, Japan koike-c@mua.biglobe.ne.jp

The presence of amorphous silicate particles in interstellar and circumstellar space has been suggested based on the observation of 9.7 and 18 μm emission bands. We have successfully synthesized amorphous silicate samples of an enstatite and forsterite composition by the mechanical milling of mixed powder consisting of SiO2–MgO and SiO2–Mg(OH)2 reagent-grade particles under different rotation frequencies and milling times. These two types of starting materials are prepared to study the effect of the OH bond on synthesis and crystallization. The amorphous samples were characterized by X-ray diffraction and infrared spectroscopy. Amorphous samples with enstatite composition are synthesized from both SiO2–MgO and SiO2–Mg(OH)2 at 300 rpm and for 300 hr. Amorphous samples with forsterite composition are synthesized from both SiO2–MgO and SiO2–Mg(OH)2. The samples from SiO2–Mg(OH)2 require 400 rpm and a long milling time of 1600 hr. After crystallization, amorphous samples with an enstatite composition synthesized from SiO2–Mg(OH)2 mainly transform into forsterite with small amounts of amorphous silica SiO2 and enstatite depending on the rotation frequencies and milling time, while those from SiO2–MgO become enstatite. The amorphous samples with a forsterite composition are crystallized to forsterite from both starting materials. The presence of H2O or OH bonds significantly affects the final products after the crystallization of amorphous silicates of enstatite composition.

Miniaturized high-resolution dual 2D MEMS mirror scanning confocal Raman microscopy for topographic and Raman mapping

1Zhang, Guozhuo,1Wang, Xu,1Wang, Yun,1Cui, Han,1Zhao, Weiqian,1Qiu, Lirong
Measurement: Journal of the International Measurement Confederation 224, 113807 Link to Article [DOI 10.1016/j.measurement.2023.113807]
1MIIT Key Laboratory of Complex-field Intelligent Exploration, School of Optics and Photonics, Beijing Institute of Technology, Beijing, 100081, China

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Hydrogen Isotopic Composition of Hydrous Minerals in Asteroid Ryugu

1Laurette Piani et al. (>10)
The Astrophysical Journal Letters 946, L43 Open Access Link to Article [DOI 10.3847/2041-8213/acc393]
1Centre de Recherches Pétrographiques et Géochimiques, CNRS—Université de Lorraine; F-54500 Nancy, France

Rock fragments of the Cb-type asteroid Ryugu returned to Earth by the JAXA Hayabusa2 mission share mineralogical, chemical, and isotopic properties with the Ivuna-type (CI) carbonaceous chondrites. Similar to CI chondrites, these fragments underwent extensive aqueous alteration and consist predominantly of hydrous minerals likely formed in the presence of liquid water on the Ryugu parent asteroid. Here we present an in situ analytical survey performed by secondary ion mass spectrometry from which we have estimated the D/H ratio of Ryugu’s hydrous minerals, D/HRyugu, to be [165 ± 19] × 10−6, which corresponds to δDRyugu = +59 ± 121‰ (2σ). The hydrous mineral D/HRyugu’s values for the two sampling sites on Ryugu are similar; they are also similar to the estimated D/H ratio of hydrous minerals in the CI chondrites Orgueil and Alais. This result reinforces a link between Ryugu and CI chondrites and an inference that Ryugu’s samples, which avoided terrestrial contamination, are our best proxy to estimate the composition of water at the origin of hydrous minerals in CI-like material. Based on this data and recent literature studies, the contribution of CI chondrites to the hydrogen of Earth’s surficial reservoirs is evaluated to be ∼3%. We conclude that the water responsible for the alteration of Ryugu’s rocks was derived from water ice precursors inherited from the interstellar medium; the ice partially re-equilibrated its hydrogen with the nebular H2 before being accreted on the Ryugu’s parent asteroid.

Distribution of s-, r-, and p-process Nuclides in the Early Solar System Inferred from Sr Isotope Anomalies in Meteorites

1,2Jonas M. Schneider,1,2Christoph Burkhardt,1,2 Thorsten Kleine
The Astrophysical Journal Letters 952, 1 Open Access Link to Article [DOI 10.3847/2041-8213/ace187]
1Max Planck Institute for Solar System Research, Justus-von-Liebig-Weg 3, D-37077 Göttingen, Germany
2Institute for Planetology, University of Münster, Wilhelm-Klemm-Straße 10, D-48149 Münster, Germany

Nucleosynthetic isotope anomalies in meteorites allow distinguishing between the noncarbonaceous (NC) and carbonaceous (CC) meteorite reservoirs and show that correlated isotope anomalies exist in both reservoirs. It is debated, however, whether these anomalies reflect thermal processing of presolar dust in the disk or are primordial heterogeneities inherited from the solar system’s parental molecular cloud. Here, using new high-precision 84Sr isotope data, we show that NC meteorites, Mars, and the Earth and Moon are characterized by the same 84Sr isotopic composition. This 84Sr homogeneity of the inner solar system contrasts with the well-resolved and correlated isotope anomalies among NC meteorites observed for other elements, and most likely reflects correlated s- and (r, p)-process heterogeneities leading to 84Sr excesses and deficits of similar magnitude, which cancel each other out. For the same reason there is no clearly resolved 84Sr difference between NC and CC meteorites, because in some carbonaceous chondrites the characteristic 84Sr excess of the CC reservoir is counterbalanced by an 84Sr deficit resulting from s-process variations. Nevertheless, most carbonaceous chondrites exhibit 84Sr excesses, which reflect admixture of refractory inclusions and more pronounced s-process heterogeneities in these samples. Together, the correlated variation of s- and (r, p)-process nuclides revealed by the 84Sr data of this study refute an origin of these isotope anomalies solely by processing of presolar dust grains, but points to primordial mixing of isotopically distinct dust reservoirs as the dominant process producing the isotopic heterogeneity of the solar system.

Origin of Isotopic Diversity among Carbonaceous Chondrites

1,2Jan L. Hellmann,1,3Jonas M. Schneider,1,3Elias Wölfer,3Joanna Drążkowska,1Christian A. Jansen,1,3Timo Hopp,1,3Christoph Burkhardt,1,3Thorsten Kleine
The Astrophysical Journal 946, L34 Open Access Link to Article [DOI 10.3847/2041-8213/acc102]
1Institut für Planetologie, University of Münster, Wilhelm-Klemm-Str. 10, D-48149 Münster, Germany;
2Department of Geology, University of Maryland, 8000 Regents Drive, College Park, MD 20742, USA
3Max Planck Institute for Solar System Research, Justus-von-Liebig-Weg 3, D-37077 Göttingen, Germany

Carbonaceous chondrites are some of the most primitive meteorites and derive from planetesimals that formed a few million years after the beginning of the solar system. Here, using new and previously published Cr, Ti, and Te isotopic data, we show that carbonaceous chondrites exhibit correlated isotopic variations that can be accounted for by mixing among three major constituents having distinct isotopic compositions, namely refractory inclusions, chondrules, and CI chondrite-like matrix. The abundances of refractory inclusions and chondrules are coupled and systematically decrease with increasing amount of matrix. We propose that these correlated abundance variations reflect trapping of chondrule precursors, including refractory inclusions, in a pressure maximum in the disk, which is likely related to the water ice line and the ultimate formation location of Jupiter. The variable abundance of refractory inclusions/chondrules relative to matrix is the result of their distinct aerodynamical properties resulting in differential delivery rates and their preferential incorporation into chondrite parent bodies during the streaming instability, consistent with the early formation of matrix-poor and the later accretion of matrix-rich carbonaceous chondrites. Our results suggest that chondrules formed locally from isotopically heterogeneous dust aggregates, which themselves derive from a wide area of the disk, implying that dust enrichment in a pressure trap was an important step to facilitate the accretion of carbonaceous chondrite parent bodies or, more generally, planetesimals in the outer solar system.

Comet 81P/Wild 2: A record of the Solar System’s wild youth

1Ryan C. Ogliore
Geochemistry (Chemie der Erde) (in Press) Link to Article [https://doi.org/10.1016/j.chemer.2023.126046]
1McDonnell Center for the Space Sciences, Washington University in St. Louis, 1 Brookings Dr., St. Louis 63130, MO, USA
Copyright Elsevier

NASA’s Stardust mission returned rocky material from the coma of comet 81P/Wild 2 (pronounced “Vilt 2”) to Earth for laboratory study on January 15, 2006. Comet Wild 2 contains volatile ices and likely accreted beyond the orbit of Neptune. It was expected that the Wild 2 samples would contain abundant primordial molecular cloud material—interstellar and circumstellar grains. Instead, the interstellar component of Wild 2 was found to be very minor, and nearly all of the returned particles formed in broad and diverse regions of the solar nebula. While some characteristics of the Wild 2 material are similar to primitive chondrites, its compositional diversity testifies to a very different origin and evolution history than asteroids. Comet Wild 2 does not exist on a continuum with known asteroids. Collisional debris from asteroids is mostly absent in Wild 2, and it likely accreted dust from the outer and inner Solar System (across the putative gap created by a forming Jupiter) before dispersal of the solar nebula. Comets are a diverse set of bodies, and Wild 2 may represent a type of comet that accreted a high fraction of dust processed in the young Solar System.

Mid-Infrared Spectroscopy of Sulfidation Reaction Products and Implications for Sulfur on Mercury

1,2Christian J. Renggli,3Aleksandra N. Stojic,3Andreas Morlok,1Jasper Berndt,3Iris Weber,1Stephan Klemme,3Harald Hiesinger
Journal of Geophysical Research (Planets)(in Press) Open Access Link to Article [https://doi.org/10.1029/2023JE007895]
1Institut für Mineralogie, Universität Münster, Münster, Deutschland
2Max Planck Institut für Sonnensystemforschung, Göttingen, Deutschland
3Institut für Planetologie, Universität Münster, Münster, Deutschland
Published by arrangement with John Wiley & Sons

We propose that the observed enrichment of sulfur at the surface of Mercury (up to 4 wt.%) is the product of silicate sulfidation reactions with a S-rich reduced volcanogenic gas phase. Here, we present new experiments on the sulfidation behavior of olivine, diopside, and anorthite. We investigate these reaction products, and those of sulfidized glasses with Mercury compositions previously reported, by mid-IR reflectance spectroscopy. We investigate both the reacted bulk materials as powders as well as cross-sections of the reaction products by in situ micro-IR spectroscopy. The mid-IR spectra confirm the presence of predicted reaction products including quartz. The mid-IR reflectance of sulfide reaction products, such as CaS (oldhamite) or MgS (niningerite), is insufficient to be observed in the complex run products. However, the ESA/JAXA BepiColombo mission to Mercury will be able to test our hypothesis by investigating the correlated abundances of sulfides with other reaction products such as quartz.

Nanoscale constraints on the nucleation and evolution of granular zircon from reidite in impactites at the Chicxulub impact structure

1Jiawei Zhao et al. (>10)
Earth and Planetary Science Letters 626, 118507 Link to Article [https://doi.org/10.1016/j.epsl.2023.118507]
1State Key Laboratory of Geological Processes and Mineral Resources, Planetary Science Institute, School of Earth Sciences, China University of Geosciences, Wuhan, 430074, China
2Space Science and Technology Centre, The Institute for Geoscience Research, School of Earth and Planetary Science, Curtin University, GPO Box U1987, Perth, WA 6845, Australia
Copyright Elsevier

Zircon with granular texture from hypervelocity impact structures can be used to estimate the thermodynamic conditions of impact processes, including pressure and temperature, and in some cases the timing of impact events via U-Pb geochronology. However, two disparate formation models have been proposed to explain the occurrence of zircon neoblasts that preserve systematic orientation relations; one involves zircon-reidite phase transformations (FRIGN zircon), whereas the other features melting and thermal dissociation of zircon in the absence of reidite. Distinguishing between these models is hampered by the lack of observational constraints on the intermediate transformation steps at nanoscale, and what processes give rise to observed systematic orientation relations among zircon neoblasts. Here we report new analyses of reidite-bearing and granular zircons from peak ring core samples of the Chicxulub impact structure using nanoscale methods. We describe lamellar and lense-like reidite habits associated with reidite twins in shocked zircon from impact melt-bearing breccia, along with the first observation of nanoscale zircon granules forming locally within preserved reidite lamellae. The crystallographic orientation of the zircon nano-granules matches the orientations predicted by the FRIGN zircon model, confirming they formed directly by solid-state reversion of reidite to zircon, and represent the earliest stages of the formation of granular zircon. Minor occurrences of baddeleyite at the interface of reidite and neoblastic zircon domains suggest that the reversion of reidite to zircon can occur together with local ZrSiO4 dissociation driven either by the loss of SiO2, which creates excess zirconia, or by local thermal dissociation of reidite. Other partially- and fully-granular zircon grains from the same impact melt-bearing breccia also preserve systematic orientation relationships among zircon neoblasts, consistent with having transformed directly from reidite. The observation that zircon neoblasts maintain systematic orientations from nanoscale to microscale in granular zircon supports the idea that neoblast orientations are encoded at the nucleation stage via solid state phase transformation. Observations in this study provide direct evidence to explain the nature of systematic high-pressure phase transitions involving zircon and have implications for unraveling the pressure-temperature history of zircon phase transitions in large impacts on Earth or other planetary bodies.