Fire-Induced Thermal Alteration in Iron Meteorites: Metallographic Analysis of the 2018 Disaster at the National Museum of Rio de Janeiro

1Felipe Abrahão Monteiro, 2Maria Elizabeth Zucolotto, 1Amanda Araujo Tosi
Anuário do Instituto de Geociências (in Press)
Open Access Link to Article [DOI: 10.11137/1982-3908_2026_49_71839]
1Universidade Federal do Rio de Janeiro, Instituto de Geociências, Departamento de Geologia, RJ, Rio de Janeiro, Brazil
2Universidade Federal do Rio de Janeiro, Museu Nacional, Departamento de Geologia e Paleontologia, Setor de Meteoritos, RJ, Rio de Janeiro, Brazil

We currently do not have a copyright agreement with this publisher and cannot display the abstract here

Revisiting chondrule formation ages using plagioclase chemistry as an indicator of thermal metamorphic overprint

1Kohei Fukuda
Japanese Magazine of Mineralogical and Petrological Sciences (in Press)
Open Access Link to Article [DOI: 10.2465/gkk.260113]
1Forefront Research Center, Graduate School of Science, The University of Osaka, 1–1 Machikaneyama-cho, Osaka, Toyonaka, 560–0043, Japan

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Trial production of the S-type asteroid regolith simulator based on ordinary chondrites

1,2Zhi-Peng Han, 1,2De-Han Shen, 3Dong-Liang Zhang, 4Guang-Ming Song, 4Chuan Chen, 5Zi-Zheng Gong, 1Shi-Jie Li
Bulletin of Mineralogy, Petrology and Geochemistry (in Press)
Link to Article [DOI: 10.3724/j.issn.1007-2802.20250040]
1Center for Lunar and Planetary Sciences, Institute of Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences, Guiyang, 550081, China
2University of Chinese Academy of Sciences, Beijing, 100049, China
3Key Laboratory of Metallogenic Prediction of Nonferrous Metals, Ministry of Education, School of Geosciences and Info-physics, Central South University, Changsha, 410083, China
4Beijing Institute of Spacecraft Environment Engineering, Beijing, 100094, China
5Deep Space Exploration Lab., Beijing, 100089, China

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Variations in nitrogen speciation in carbonaceous chondritic materials and their origins: Insights from partial fluorescence yield X-ray absorption spectra of nitrogen K-edge

1Yoko Kebukawa, 2Hiroki Suga, 1,3Masanori Suzuki, 3Minori Ogino, 4Michael E. Zolensky, 5Yoshio Takahashi
Geochemical Journal (in Press)
Open Access Link to Article [DOI: 10.2343/geochemj.GJ26009]
1Department of Earth and Planetary Sciences, Institute of Science Tokyo, 2-12-1 Ookayama, Meguro-ku, Tokyo, 152-8551, Japan
2NanoTerasu Promotion Division, Japan Synchrotron Radiation Research Institute, 468-1 Aramaki-Aza-Aoba, Aoba-ku, Miyagi, Sendai, 980-8572, Japan
3Department of Chemistry and Life Science, Yokohama National University, 79-5 Tokiwadai, Hodogaya-ku, Yokohama, 240-8501, Japan
4Astromaterials Research and Exploration Science, NASA Johnson Space Center, Houston, 77058, TX, United States
5Department of Earth and Planetary Science, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan

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Petrology, Geochemistry, and Geochronology of the L6 Ordinary Chondrite Maoming Meteorite

1Cheng Yue, 1Xiaohao Che, 1Tao Long, 2Ziyao Wang, 1Huimin Wang, 1Chen Wang, 1Dunyi Liu
Acta Geoscientica Sinica (in Press) Link to Article [DOI: 10.3975/cagsb.2026.032421]
1Institute of Geology, Chinese Academy of Geological Sciences, Beijing, 100037, China
2Hebei GEO University, Hebei, Shijiazhuang, 052161, China

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Characterization of Northwest Africa 6410 L6 ordinary chondrite using scanning electron microscopy, X-ray diffraction and Mössbauer spectroscopy

1A. A. Maksimova, 1E. V. Petrova, 1A. V. Chukin, 2G. Varga, 2Z. Dankházi, 1,3,4M. Gritsevich, 5E. Kuzmann, 5Z. Homonnay, 1M. I. Oshtrakh
Meteoritics & Planetary Science, (in Press), 1–15 Link to Article [DOI: 10.1111/maps.70258]
1Institute of Physics and Technology, Ural Federal University, Ekaterinburg, Russian Federation
2Department of Materials Physics, Eötvös Loránd University, Budapest, Hungary
3Instituto de Astrofísica de Andalucía (IAA-CSIC), Granada, Spain
4Finnish Fireball Network, Ursa Astronomical Association, Helsinki, Finland
5Laboratory of Nuclear Chemistry, Institute of Chemistry, Eötvös Loránd University, Budapest, Hungary

Published by arrangement with John Wiley & Sons

Ordinary chondrites preserve important information on the mineralogical and phase evolution as well as thermal metamorphism of their parent bodies. Quantitative characterization of minerals/phases and cation distributions in silicates using complementary analytical techniques provides valuable constraints on their crystal chemistry and thermal history. In this study, we investigate the Northwest Africa (NWA) 6410 L6 ordinary chondrite using optical microscopy, scanning electron microscopy (SEM) with energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), and 57Fe Mössbauer spectroscopy. Optical microscopy revealed significant porosity of the polished section together with abundant chondrules and chondrule relics. The mineralogical/phase composition and crystal chemistry of the meteorite were characterized by SEM, EDS, XRD, and Mössbauer spectroscopy. XRD identified the major mineral phases, whereas Mössbauer spectroscopy resolved the Fe-bearing mineral/phase compounds and the distribution of Fe2+ between the M1 and M2 crystallographic sites in olivine and orthopyroxene. The occupancies of Fe2+ and Mg2+ at the M1 and M2 sites were determined from XRD refinements, while the ratios of Fe2+ site populations in silicates were derived from Mössbauer spectra. The Fe2+ M1/M2 site-occupancy ratios obtained independently by XRD and Mössbauer spectroscopy are in good agreement, demonstrating the consistency of the two approaches. The temperatures of cation equilibrium distribution calculated from XRD and Mössbauer spectroscopy are 570 and 626 K, respectively, for olivine and 679 and 686 K, respectively, for orthopyroxene. Classification based on the relative spectral areas (roughly the relative Fe fractions) of characteristic Mössbauer components confirms that NWA 6410 belongs to the L group of ordinary chondrites.

Distribution and rare earth element abundances of apatite in Bennu samples determined by synchrotron X-ray fluorescence spectroscopy

1B. J. Tkalcec (>10)
Meteoritics & Planetary Science, (in Press), 1–23
Open Source Link to Article [DOI: 10.1111/maps.70259]
1Schwiete Cosmochemistry Laboratory, Goethe University, Frankfurt am Main, Germany

Published by arrangement with John Wiley & Sons

Apatite is often the most rare earth element (REE)-enriched mineral in chondritic meteorites. REE enrichment and fractionation levels in apatite grains can give insight into the aqueous fluids in which they formed and the conditions prevailing within the host body. In this study, we applied synchrotron X-ray fluorescence (SXRF) spectroscopy to investigate the distribution and REE enrichments of 34 apatite grains in five rock fragments from asteroid (101955) Bennu, collected and brought to Earth by NASA’s OSIRIS-REx mission. We observe a strongly heterogeneous apatite distribution with frequent occurrence of clusters containing three to nine apatite grains. SXRF results reveal a wide grain-to-grain range of REE enrichment levels, at 15–900 times those of bulk CI chondrites. Of the 34 measured apatite grains, four are Mn-enriched (Mn > 1.26 wt%) and these show the lowest REE concentrations (15–65 times CI). Little light/heavy REE fractionation is observed in the Bennu apatite grains, in contrast to the heavy REE enrichment observed in apatite grains in samples from asteroid Ryugu. Our results suggest fluid circulation in Bennu’s parent asteroid involved apatite precipitation in cavities and local variations in water-rock interaction leading to local changes in fO2, and fluid chemistry. Given the dynamically evolving fluid conditions and the enhanced peripheral luminescence and oscillatory zoning observed in some apatite grains, an absence of REE fractionation during apatite formation appears unlikely. We postulate that, as fluid chemistry evolved to higher alkalinity and salinity, sequential complexation resulted in early incorporation of light REEs into precipitating apatite grains, subsequently balanced by later adsorption of heavy REEs.