Primitive asteroids and carbonaceous chondrites (CCs) record the history of processes in the early solar system. Visible and shortwave infrared (VSWIR) spectroscopy of primitive asteroids and bulk-powdered CCs has identified shared spectral features suggestive of shared parent body origins. However, bulk powder CC spectra are spatially unresolved and destroy textures, which hinders tying shared spectral features to particular phases, petrologic contexts, and alteration histories. This study analyzes 20 CCs measured using microimaging hyperspectral VSWIR spectroscopy, recording over 700,000 individual spectra at the ∼80 μm/pixel scale. We compare CC spectral features with asteroids using the Expanded Bus-DeMeo taxonomy. We introduce a spectral processing pipeline using Savitzky-Golay filtering to better capture subtle spectral features, reduce noise and enhance comparisons between asteroid classes and CC subgroups and constituent phases. Key findings include a close spectral match between CM chondrites and Cgh-class asteroids, as well as between CV3 chondrites and L-class asteroids. Unaltered, iron-bearing silicate CC components are similar to “stony” asteroid spectral classes. Furthermore, taxonomy-based separation of CC spectra also identifies features unique to CCs, for example, oxidized iron signatures in CR2 chondrite NWA 7502 and other samples indicative of terrestrial weathering. Together these CC data show that primary and secondary Fe-bearing minerals drive the separations in the asteroid classes expressed in the Expanded Bus-DeMeo taxonomy. These findings also underscore the value of microimaging spectroscopy and statistically motivated frameworks in conducting larger surveys to interrogate the shared record of alteration in the early solar system. The data set is released for further study.
{"title":"Microimaging Spectroscopy of Carbonaceous Chondrites and Comparison to the Spectral Diversity of Asteroids","authors":"S. A. Parra, R. N. Greenberger, B. L. Ehlmann","doi":"10.1029/2025JE009048","DOIUrl":"10.1029/2025JE009048","url":null,"abstract":"<p>Primitive asteroids and carbonaceous chondrites (CCs) record the history of processes in the early solar system. Visible and shortwave infrared (VSWIR) spectroscopy of primitive asteroids and bulk-powdered CCs has identified shared spectral features suggestive of shared parent body origins. However, bulk powder CC spectra are spatially unresolved and destroy textures, which hinders tying shared spectral features to particular phases, petrologic contexts, and alteration histories. This study analyzes 20 CCs measured using microimaging hyperspectral VSWIR spectroscopy, recording over 700,000 individual spectra at the ∼80 μm/pixel scale. We compare CC spectral features with asteroids using the Expanded Bus-DeMeo taxonomy. We introduce a spectral processing pipeline using Savitzky-Golay filtering to better capture subtle spectral features, reduce noise and enhance comparisons between asteroid classes and CC subgroups and constituent phases. Key findings include a close spectral match between CM chondrites and Cgh-class asteroids, as well as between CV3 chondrites and L-class asteroids. Unaltered, iron-bearing silicate CC components are similar to “stony” asteroid spectral classes. Furthermore, taxonomy-based separation of CC spectra also identifies features unique to CCs, for example, oxidized iron signatures in CR2 chondrite NWA 7502 and other samples indicative of terrestrial weathering. Together these CC data show that primary and secondary Fe-bearing minerals drive the separations in the asteroid classes expressed in the Expanded Bus-DeMeo taxonomy. These findings also underscore the value of microimaging spectroscopy and statistically motivated frameworks in conducting larger surveys to interrogate the shared record of alteration in the early solar system. The data set is released for further study.</p>","PeriodicalId":16101,"journal":{"name":"Journal of Geophysical Research: Planets","volume":"131 2","pages":""},"PeriodicalIF":4.0,"publicationDate":"2026-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://agupubs.onlinelibrary.wiley.com/doi/epdf/10.1029/2025JE009048","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146136042","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Recent studies challenge the classical view of the Moon as lacking ferric iron (Fe3+). Laboratory investigations and remote sensing data confirm the presence of Fe3+, but its evolutionary mechanisms are not fully understood. We propose a temperature-dependent mechanism for the evolution of iron content and valence in the assembly of clinopyroxene-glass from Chang'e 5 lunar regolith samples. In situ heating experiments using transmission electron microscopy coupled with electron energy loss spectroscopy showed that heating from 23°C to 1,000°C reduced clinopyroxene's Fe concentration from 7.73% to 5.59%, while its Fe3+/∑Fe (∑Fe = Fe3+ + Fe2+) ratio increased from 30.17% to 59.74%. Concurrently, the Fe content in adjacent glass decreased at higher temperatures, with a significant drop in its Fe3+/∑Fe ratio from 22.81% at 700°C to 3.93% at 900°C. These findings indicate a heating-induced co-evolution of iron in lunar glass and clinopyroxene, suggesting that the impact-induced thermal evolution of Fe3+ may influence the lunar surface's local redox state.
{"title":"Temperature-Dependent Evolution of Iron Content and Valence Between Clinopyroxene and Glass on the Moon","authors":"Jiaxin Xi, Shan Li, Haiyang Xian, Yiping Yang, Dongsheng He, Jianxi Zhu, Xiaoju Lin, Hongmei Yang, Hongping He","doi":"10.1029/2025JE009174","DOIUrl":"https://doi.org/10.1029/2025JE009174","url":null,"abstract":"<p>Recent studies challenge the classical view of the Moon as lacking ferric iron (Fe<sup>3+</sup>). Laboratory investigations and remote sensing data confirm the presence of Fe<sup>3+</sup>, but its evolutionary mechanisms are not fully understood. We propose a temperature-dependent mechanism for the evolution of iron content and valence in the assembly of clinopyroxene-glass from Chang'e 5 lunar regolith samples. In situ heating experiments using transmission electron microscopy coupled with electron energy loss spectroscopy showed that heating from 23°C to 1,000°C reduced clinopyroxene's Fe concentration from 7.73% to 5.59%, while its Fe<sup>3+</sup>/∑Fe (∑Fe = Fe<sup>3+</sup> + Fe<sup>2+</sup>) ratio increased from 30.17% to 59.74%. Concurrently, the Fe content in adjacent glass decreased at higher temperatures, with a significant drop in its Fe<sup>3+</sup>/∑Fe ratio from 22.81% at 700°C to 3.93% at 900°C. These findings indicate a heating-induced co-evolution of iron in lunar glass and clinopyroxene, suggesting that the impact-induced thermal evolution of Fe<sup>3+</sup> may influence the lunar surface's local redox state.</p>","PeriodicalId":16101,"journal":{"name":"Journal of Geophysical Research: Planets","volume":"131 2","pages":""},"PeriodicalIF":4.0,"publicationDate":"2026-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146135866","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Throughout Gale crater on Mars, the Curiosity rover has found high abundances (15–73 wt%) of X-ray amorphous materials in the rocks and sediments. The composition of this amorphous fraction is primarily calculated by subtracting crystalline abundances measured by the Chemistry & Mineralogy X-Ray Diffractometer (CheMin) from bulk elemental abundances from the Alpha Particle X-Ray Spectrometer (APXS). If any crystalline phase was underrepresented in the CheMin data, the elemental components of that phase would be overestimated in the amorphous fraction. This study examines the possibility of underrepresented crystalline phases in X-ray diffraction data using mixtures of amorphous ferric sulfate (AFS) and crystalline Ca-sulfate. Two compositionally equivalent mixtures were made with different morphologies: first, a simple mixture of AFS and Ca-sulfate grains and second, Ca-sulfate grains with AFS coatings. Each mixture was characterized with Raman spectroscopy, and two X-ray diffractometers (XRDs): a Bragg-Brentano instrument with CuKα radiation and a Debye-Scherrer instrument with CoKα radiation. Raman peaks from Ca-sulfate dominate both mixtures, but are dampened when AFS coats the Ca-sulfate grains. In XRD data, AFS coatings cause an overestimation of the amorphous percentage, with a difference between the known and refined amorphous abundances of 29–34 wt%, compared to 2–2.8 wt% for the uncoated mixtures. The effects of the coatings were slightly amplified with the Debye-Scherrer XRD, primarily due to the increased scattering and absorption of the CoKα radiation. This has implications for interpreting the XRD data of mixed amorphous-crystalline samples on Mars, as any Fe-rich amorphous coating may cause an overestimation of the amorphous abundance.
{"title":"Obscuration of Crystalline Ca-Sulfate in XRD and Raman Data When Coated by Amorphous Ferric Sulfate: Implications for the Amorphous Components at Gale Crater","authors":"R. J. Hopkins, A. D. Rogers, L. Ehm","doi":"10.1029/2025JE009299","DOIUrl":"https://doi.org/10.1029/2025JE009299","url":null,"abstract":"<p>Throughout Gale crater on Mars, the <i>Curiosity</i> rover has found high abundances (15–73 wt%) of X-ray amorphous materials in the rocks and sediments. The composition of this amorphous fraction is primarily calculated by subtracting crystalline abundances measured by the Chemistry & Mineralogy X-Ray Diffractometer (CheMin) from bulk elemental abundances from the Alpha Particle X-Ray Spectrometer (APXS). If any crystalline phase was underrepresented in the CheMin data, the elemental components of that phase would be overestimated in the amorphous fraction. This study examines the possibility of underrepresented crystalline phases in X-ray diffraction data using mixtures of amorphous ferric sulfate (AFS) and crystalline Ca-sulfate. Two compositionally equivalent mixtures were made with different morphologies: first, a simple mixture of AFS and Ca-sulfate grains and second, Ca-sulfate grains with AFS coatings. Each mixture was characterized with Raman spectroscopy, and two X-ray diffractometers (XRDs): a Bragg-Brentano instrument with CuKα radiation and a Debye-Scherrer instrument with CoKα radiation. Raman peaks from Ca-sulfate dominate both mixtures, but are dampened when AFS coats the Ca-sulfate grains. In XRD data, AFS coatings cause an overestimation of the amorphous percentage, with a difference between the known and refined amorphous abundances of 29–34 wt%, compared to 2–2.8 wt% for the uncoated mixtures. The effects of the coatings were slightly amplified with the Debye-Scherrer XRD, primarily due to the increased scattering and absorption of the CoKα radiation. This has implications for interpreting the XRD data of mixed amorphous-crystalline samples on Mars, as any Fe-rich amorphous coating may cause an overestimation of the amorphous abundance.</p>","PeriodicalId":16101,"journal":{"name":"Journal of Geophysical Research: Planets","volume":"131 2","pages":""},"PeriodicalIF":4.0,"publicationDate":"2026-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://agupubs.onlinelibrary.wiley.com/doi/epdf/10.1029/2025JE009299","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146135923","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}