Types Of Chondrites Research Articles

The non-carbonaceous nature of Earth’s late-stage accretion

Constraining the origin of Earth’s building blocks requires knowledge of the chemical and isotopic characteristics of the source region(s) where these materials accreted. The siderophile elements Mo and Ru are well suited to investigating the mass-independent nucleosynthetic (i.e., “genetic”) signatures of material that contributed to the latter stages of Earth’s formation. Studies contrasting the Mo and Ru isotopic compositions of the bulk silicate Earth (BSE) to genetic signatures of meteorites, however, have reported conflicting estimates of the proportions of the non-carbonaceous type or NC (presumptive inner Solar System origin) and carbonaceous chondrite type or CC (presumptive outer Solar System origin) materials delivered to Earth during late-stage accretion (likely including the Moon-forming event and onwards). The present study reports new mass-independent isotopic data for Mo, which are presumed to reflect the composition of the BSE. A comparison of the new estimate for the BSE composition with new data for a select suite of NC iron meteorites is used to constrain the genetic characteristics of materials accreted to Earth during late-stage accretion. Results indicate that the final 10 to 20 wt% of Earth’s accretion was dominated by NC materials that were likely sourced from the inner Solar System, although the addition of minor proportions of CC materials, as has been suggested to occur during accretion of the final 0.5 to 1 wt% of Earth’s mass, remains possible. If this interpretation is correct, it brings estimates of the genetic signatures of Mo and Ru during the final 10 to 20 wt% of Earth accretion into concordance.

Chrome-rich spinels in micrometeorites from modern Antarctic sedimentary deposits

Each year, approximately 5000 tons of extraterrestrial material reaches the Earth's surface as micrometeorites, cosmic dust particles ranging from 10 to 2000 μm in size. These micrometeorites, collected from diverse environments, mainly deep-sea sediments, Antarctic ice, snow and loose sediments, and hot deserts, are crucial in understanding our Solar System's evolution. Chrome-rich spinel (Cr-spinel) minerals have gained attention as proxies for studying the extraterrestrial flux in sedimentary deposits, because these robust minerals occur, in various extraterrestrial materials, with compositions characteristic of their parent bodies. A total of 27 Cr-spinel bearing micrometeorites within the size range of 185–800 μm, were identified from approximately 6000 micrometeorites from the Transantarctic Mountains (n = 23) and the Sør Rondane Mountains (n = 4), in Antarctica, containing Cr-spinel (8–120 μm), were examined in this study for geochemical composition and high-precision oxygen isotope ratios to assess alteration and identify potential parent bodies.Oxygen isotopes in the micrometeorite groundmass and in Cr-spinel grains reveal a predominance of ordinary chondritic precursors, with only 1 in 10 micrometeorites containing Cr-spinel minerals showing a carbonaceous chondritic signature. This may be further confirmed by an elevated Al content (> 12 wt% Al2O3) in Cr-spinel from specific carbonaceous chondrite types, but a more extensive dataset is required to establish definitive criteria. The first Cr-spinel bearing particle, in an Antarctic micrometeorite, that can be linked to R-chondrites based on oxygen isotopes, has been documented, demonstrating the potential for R-chondrites as a source of chrome-rich spinels. The study also highlights the potential for chemical modifications and alteration processes that Cr-spinel minerals may undergo during their time on the parent body, atmospheric entry, and terrestrial residence.In the context of the broader micrometeorite flux, the results align with previous findings, showing a consistent contribution of micrometeorites containing Cr-spinel minerals related to ordinary chondrites over the past 2 to 4 million years. This is however a small fraction (∼ 1 %) of the total micrometeorite flux. The study further confirms that Cr-spinel minerals recovered from sedimentary deposits serve as valuable proxies for tracking events related to ordinary chondritic or achondritic materials. However, it is emphasized that Cr-spinel minerals alone cannot serve as exclusive indicators of the overall extraterrestrial flux, especially during periods dominated by carbonaceous chondritic dust in the inner Solar System. To comprehensively understand the complete extraterrestrial flux, additional proxies are needed to trace dust-producing events associated with various Solar System objects. The intricate nature of Cr-spinel compositions, and the potential for alteration processes emphasize the need for further research to refine our understanding of these extraterrestrial markers.

Abundance, sizes, and major element compositions of components in CR and LL chondrites: Formation from single reservoirs

AbstractAbundances, apparent sizes, and individual chemical compositions of chondrules, refractory inclusions, other objects, and surrounding matrix have been determined for Semarkona (LL3.00) and Renazzo (CR2) using consistent methods and criteria on X‐ray element intensity maps. These represent the non‐carbonaceous (NC, Semarkona) and carbonaceous chondrite (CC, Renazzo) superclans of chondrite types. We compare object and matrix abundances with similar data for CM, CO, K, and CV chondrites. We assess, pixel‐by‐pixel, the major element abundance in each object and in the entire matrix. We determine the abundance of “metallic chondrules” in LL chondrites. Chondrules with high Mg/Si and low Fe/Si and matrix carrying opposing ratios complement each other to make whole rocks with near‐solar major element ratios in Renazzo. Similar Mg/Si and Fe/Si chondrule–matrix relationships are seen in Semarkona, which is within 11% of solar Mg/Si but significantly Fe‐depleted. These results provide a robust constraint in support of single‐reservoir models for chondrule formation and accretion, ruling out whole classes of astrophysical models and constraining processes of chondrite component formation and accretion into chondrite parent bodies.

Oxygen isotope study of the Asuka-881020 CH chondrite II: Porphyritic chondrules

Oxygen isotope ratios and elemental compositions of porphyritic chondrules and olivine and pyroxene fragments in the Asuka-881020 CH chondrite were analyzed. The oxygen isotope ratios inside individual porphyritic chondrules are homogeneous within the uncertainty, except for relict grains of olivine and low-Ca pyroxene that have distinct oxygen isotope ratios. The average oxygen isotope ratios of the individual chondrules plot along and above the primitive chondrule mineral (PCM) line with Δ17O (=δ17O – 0.52 × δ18O) values from −4.7 ‰ to +4.1 ‰. The olivine and pyroxene fragments, which have Δ17O values ranging from −2.1 ‰ to +3.2 ‰, are likely to be fragments of the porphyritic chondrules.Unlike the non-porphyritic chondrules in CH and CB chondrites and chondrules in other carbonaceous chondrites, the type I and II chondrules do not show a systematic difference in the Δ17O values. Furthermore, the Δ17O values of the type I chondrules increase from −4.7 ‰ to +4.1 ‰ with increasing Mg# (=molar [MgO]/[MgO + FeO] × 100) from 96 to 99. We argue that the positive Δ17O-Mg# trend is explained by an addition of 16O-poor carbon-rich organics as a reducing agent to the relatively 16O-rich precursor silicate, which is a new environment for chondrule formation. This hypothesis is supported by the two lines of evidence observed in the present study. (1) The chondrules and fragments with higher Δ17O values show larger deviations from the PCM line towards low δ18O, suggesting oxygen isotope mass fractionation between the chondrule melt and CO or CO2. (2) Olivine phenocrysts in the chondrules with high Δ17O values contain Ni-poor Fe-metal particles surrounded by silica-rich glass, which may be reduction products during the chondrule formation. Thus, it is suggested that the porphyritic chondrules in CH and CB chondrites have different origins from chondrules in any other chondrite types, even from the non-porphyritic chondrules in CH and CB chondrites.

Insights on the origin of oldhamite in enstatite meteorites from Ca stable isotopes

In order to understand the origin of oldhamite (CaS) in enstatite meteorites, we report Ca isotopic compositions (δ44/40Ca) of oldhamite (obtained from water leachate of bulk chondrites and aubrites and mineral separates from the Norton County aubrite) and silicate minerals from different types of enstatite chondrites and aubrite. The δ44/40Ca of the bulk enstatite chondrites range from 1.05 ‰ to 1.24 ‰, with an average of 1.13 ± 0.12 ‰, higher than that of the estimate of the bulk silicate earth (∼0.94 ‰). Major and trace element analyses show that the water leachates of enstatite chondrites are mainly composed of oldhamite, and they take over 20.6–68.5 % Ca of the bulk meteorite Ca budget. The Ca isotope fractionation between oldhamite and residual silicate (Δ44/40Caoldhamite-silicate) for the studied enstatite chondrites is minimum (−0.44 ‰) for Abee (impact-melt breccia) and maximum (+0.16) for St.Marks (EH5). The Ca isotope fractionation between oldhamite (individual mineral grains and leachate) and silicates in Norton County varies from −0.47 ‰ to −0.31 ‰ with an average of −0.41 ‰. These Δ44/40Caoldhamite-silicate correlate well with previous theoretical calculation and suggests that the oldhamites in Norton County are in isotopic equilibrium with co-existing silicates, and therefore were formed during magmatic processes. However, in enstatite chondrites, the large variation on Δ44/40Caoldhamite-silicate and its negative correlation with metamorphic temperature reflects the redistribution and equilibration of Ca isotopes during metamorphism. The variable Δ44/40Caoldhamite-silicate found in unequilibrated chondrites reflect kinetic Ca isotope fractionation between oldhamite and nebular gas and therefore is evidence for the formation of oldhamite by condensation in the solar nebula.

14C and 14C‐10Be terrestrial age dating system for meteorites—New data for four recently fallen meteorites

AbstractWe perform a systematic and detailed study of the 14C and 14C‐10Be dating systems for meteorite terrestrial ages. Physical model calculations indicate that neither the 14C production rates nor the 14C/10Be production rate ratios are constant enough to be reasonably approximated by average values. By using simple averages, one introduces a significant size‐dependent bias into the database for meteorite terrestrial ages. By combining modeled 14C production rates and 14C/10Be production rate ratios with (22Ne/21Ne)cos ratios and assuming ~80% ablation losses, relatively easy to use correlations of 14C production rates and 14C/10Be production rate ratios as a function of (22Ne/21Ne)cos are established. The new correlations enable the determination of terrestrial ages that are more accurate than ages based solely on average values for 14C and/or 14C/10Be. We validate the model predictions by measuring 14C activity concentrations, 14C/10Be production rate ratios, 21Necos concentrations, and (22Ne/21Ne)cos ratios in four recently fallen meteorites: Mt. Tazerzait, Boumdeid (2011), Bensour, and SaU 606. The experimental data confirmed the model predictions, although the available data are insufficient to be conclusive. More data from freshly fallen meteorites are needed for validating the model predictions for different chondrite sizes and chondrite types.

Iron Isotope Constraints on the Structure of the Early Solar System

The recent advent of nontraditional isotopic systems has revealed that meteorites display a fundamental isotopic dichotomy between noncarbonaceous (NC) and carbonaceous (C) groups, which represent material from the inner and outer solar system, respectively. On the basis of iron isotope anomalies, this view has recently been challenged in favor of a circumsolar disk structured into three distinct reservoirs (the so-called isotopic trichotomy). In this scenario, the CI chondrites—a rare type of carbonaceous chondrites with chemical composition similar to that of the Sun’s photosphere—would sample a distinct source region than other carbonaceous chondrites, located beyond Saturn’s orbit. Here, we report a model based on the available data for both mass-dependent fractionation of Te stable isotopes and mass-independent Fe nucleosynthetic anomalies. On the basis of the Te–Fe isotopic correlation defined by all carbonaceous chondrites including CIs, we show that the NC-CC dichotomy extends to Fe isotopes. Our finding thus supports (i) the existence of only two reservoirs in the early solar system and (ii) the ubiquitous presence of CI-like dust throughout the carbonaceous reservoir. Our approach also reveals that the carrier phase of 54Fe anomalies corresponds to Fe–Ni metal beads mostly located within chondrules. Finally, we propose that the CC chondrule component records a constant mix of refractory inclusions and NC-like dust.

Results of statistical analysis of primary components concentrations in bulk chemical composition of ordinary chondrite groups

AbstractWe used two different methods of statistical analysis—cluster analysis and principal component analysis—to analyze the concentrations of principal chemical components (Si, Mg, Ca, Fe, Ni) and Co in ordinary chondrites. The analysis is based predominantly on published data (metadata). In total, chemical composition data from 646 ordinary chondrites were used in the statistical analysis. The aim of this analysis was to establish whether it would be possible or not to distinguish H, L, and LL chondrites based on the concentrations of major elements and Co in their bulk chemical compositions. It was also important to determine what conclusions such an analysis could enable to draw about matter differentiation in the formation environments of primordial parent bodies of particular ordinary chondrite groups (H, L, and LL). Another aim of the statistical analysis was to determine whether the distribution of Fe and Ni (with Co admixtures) is independent of petrographic types within particular groups of chondrites. This is of crucial importance for determining the distribution of FeNi(Co) ore occurrences in potential extraterrestrial deposits on modern asteroids—the sources of ordinary chondrites. The obtained results of statistical analyses confirmed that a clear‐cut distinction between particular groups of ordinary chondrites is only possible for group H, while distinguishing L chondrites from LL chondrites is not always obvious. The results of the statistical analyses relating to the question of the possible existence of several primordial parent bodies (formation environments) of each group of ordinary chondrites are consistent with the results of contemporary astronomical spectroscopy research. What is particularly interesting is obtaining indications of the existence of common formation environments of the matter of L and LL chondrites, possibly on a few primordial parent bodies. The statistical analyses indicate that there is no correlation between the concentration of principal chemical components and the petrographic type of ordinary chondrites. This proves homogenous distributions of these elements within the parent bodies of each group of ordinary chondrites. Hence, the distribution of these elements in individual present‐day asteroids is also homogenous.

Native Nickel–Iron Metals from Lonar Crater Impactites (India) and Regolith of the Moon

The Lonar crater (India) is the best preserved and most studied on Earth, formed in basalts, which makes it possible to conduct a comparative study with impact transformations of mineral matter on the Moon and other planets of the Solar System. Comparative studies have shown that impactor material, both on the Earth and on the Moon, is present in impactites not only in a geochemically dispersed form, as previously thought, but also in the form of individual submicron particles distributed in the molten target material. These are particles of native nickel, taenite, and high-nickel kamacite, which, apparently, are the transformed material of the impactor. High-nickel submicron metal inclusions are widespread in the impactites of the Lonar crater, as they were found in all studied preparations made from materials collected from different points along the rim of the crater. The high-nickel particles found in this study are an additional argument in favor of the previously stated assumption about the chondrite type of impactor.

Silicon and iron isotopes in components of enstatite chondrites: Implications for metal–silicate–sulfide fractionation in the solar nebula

AbstractSilicon and iron isotope compositions of different physically separated components of enstatite chondrites (EC) were determined in this study to understand the role of nebular and planetary scale events in fractionating Si and Fe isotopes of the terrestrial planet‐forming region. We found that the metal–sulfide nodules of EC are strongly enriched in light Si isotopes (δ30Si ≥ −5.61 ± 0.12‰, 2SD), whereas the δ30Si values of angular metal grains, magnetic, slightly magnetic, and non‐magnetic fractions become progressively heavier, correlating with their Mg# (Mg/(Mg+Fe)). White mineral phases, composed primarily of SiO2 polymorphs, display the heaviest δ30Si of up to +0.23 ± 0.10‰. The data indicate a key role of metal–silicate partitioning on the Si isotope composition of EC. The overall lighter δ30Si of bulk EC compared to other planetary materials can be explained by the enrichment of light Si isotopes in EC metals along with the loss of isotopically heavier forsterite‐rich silicates from the EC‐forming region. In contrast to the large Si isotope heterogeneity, the average Fe isotope composition (δ56Fe) of EC components was found to vary from −0.30 ± 0.08‰ to +0.20 ± 0.04‰. A positive correlation between δ56Fe and Ni/S in the components suggests that the metals are enriched in heavy Fe isotopes whereas sulfides are the principal hosts of light Fe isotopes in the non‐magnetic fractions of EC. Our combined Si and Fe isotope data in different EC components reflect an inverse correlation between δ30Si and δ56Fe, which illustrates that partitioning of Si and Fe among metal, silicate, and sulfidic phases has significantly fractionated Si and Fe isotopes under reduced conditions. Such isotope partitioning must have occurred before the diverse components were mixed to form the EC parent body. Evaluation of diffusion coefficients of Si and Fe in the metal and non‐metallic phases suggests that the Si isotope compositions of the silicate fractions of EC largely preserve information of their nebular processing. On the other hand, the Fe isotopes might have undergone partial or complete re‐equilibration during parent body metamorphism. The relatively uniform δ56Fe among different types of bulk chondrites and the Earth, despite Fe isotope differences among their components, demonstrates that the chondrite parent bodies were not formed by random mixing of chondritic components from different locations in the disk. Instead, the chondrite components mostly originated in the same nebular reservoir and Si and Fe isotopes were fractionated either due to gas–solid interactions and associated changes in physicochemical environment of the nebular reservoir and/or during parent body processing. The heavier Si isotope composition of the bulk silicate Earth may require accretion of chondritic and/or isotopically heavier EC silicates along with cumulation of refractory forsterite‐rich heavier silicates lost from the EC‐forming region to form the silicate reservoir of the Earth.

The Spectrum and Orbit of a Fireball Producing Mesospheric Irregularity and Implications for Meteor Mass Deposition

The physical properties of meteoroids producing meteor plasma non-field-aligned irregularities (NFAI) in the Earth’s atmosphere are poorly known. Here we report a complete picture of a fireball and mesospheric NFAI that it produced for the first time. Simultaneous radar and optical observations were made by the recently completed facility, Meteor and ionospheric Irregularity Observation System. The observations show that the mesospheric NFAI were clustered into three patches where the optical meteor flares took place, instead of being generated continuously along the whole meteor path. It is very likely that nanometer-or-larger-sized dust particles could be directly generated via meteoroid fragmentation at the flaring points and thus promote the generation of NFAI patches. The properties of the parent meteoroid show a chondrite type and a Jupiter family comet orbit, with Na/Mg and Fe/Mg intensity ratios of 1.5 and 1, respectively, photometric mass of about 4 g, and fragmentation strengths of around 10–74 kPa. The results suggest that the direct generation of dust particles, which was previously observed in the atmospheric disintegration of a kiloton-scale meteoroid, could be extended to the much smaller gram-scale meteoroids. Since meteoroids having such characteristics or more fragile material are not unusual, further studies leading to a better understanding of meteor mass deposition in the upper atmosphere, which consider the dust particles directly generated via gram-scale meteoroid fragmentation, are extremely important.

How Mössbauer spectroscopy can be of value to industry to select extraterrestrial objects for natural resources

Space agencies are working on the project of capturing asteroids which contain natural resources valuable for industry. Based on studies of meteorites samples it was determined that the most useful source of raw materials for this purpose could be parent bodies of ordinary chondrites of type H. The identification of the type of ordinary chondrites with the use of a classical method (determination of the Fa/Fs ratio (fayalite versus ferrosilite) by electron microprobe measurements) cannot be performed on the surface of asteroids due to technical reasons. It may, however, be done based on Mössbauer measurements followed by the application of the 4M method. The name of the method – 4M, comes from four words: Meteorites, Mössbauer spectroscopy, Multidimensional discriminant analysis and Mahalanobis distance. Following the success of Mössbauer spectroscopy in the mission on Mars, there are suggestions to use the same method for the investigation of the surface of asteroids. In our experimental study, in which five Mössbauer laboratories took part, we assessed the effectiveness and reliability of the 4M method by comparison of the results obtained by Mössbauer studies of ordinary chondrites of type H, L and LL. Details of the study and problems related to the effectiveness of the 4M method are discussed.

Raman Spectroscopy Studies of Equilibrated Ordinary Chondrites with H and L Group and Shock Metamorphism Degrees

Ordinary chondrites are the most common type of chondrites. As a non-destructive, rapid, and semi-quantitative technology, Raman spectroscopy is widely used in geoscience. This paper presents the results of a Raman spectroscopic study that we conducted for 16 ordinary chondrites with different chemical groups and variable degrees of shock metamorphism. We found that: (1) the relationship between the Fe composition of olivine and pyroxene and the characteristic peaks of the Raman spectrum established by predecessors cannot be refined to the range of meteorites, the shock on meteorites also affects the Raman spectral characteristics of minerals and (2) the full width at half maximum (FWHM) of the shocked minerals (including high-pressure minerals) in meteorites increases in the Raman spectrum, however, no clear numerical relationship with pressure was found. Based on these data, we assess that the feasibility of Raman spectroscopy for the classification of chemical group and shock metamorphism in ordinary chondrites is not well established.

Nickel-rich, volatile depleted iron meteorites: Relationships and formation processes

Ungrouped iron meteorites Tishomingo, Willow Grove, and Chinga, and group IVB iron meteorites, are Ni-rich. Similarities include enrichments of 10–100 × CI for some refractory siderophile elements, and equivalent depletions in more volatile siderophile elements. Superimposed on the overall enrichment/depletion trend, certain siderophile elements (P, W, Fe, Mo) are depleted relative to elements of similar volatility. All three ungrouped irons derive from parent bodies formed in the early Solar System. Willow Grove and Chinga are characterized by cosmic ray exposure corrected 182W/184W consistent with metal-silicate segregation on their parent bodies within 1–3 Myr of Solar System formation, within the age range determined for segregation of magmatic iron meteorite parent bodies, including group IVB irons. Tishomingo is characterized by a younger model age 4–5 Myr subsequent to Solar System formation, reflecting either late stage melting resulting from 26Al decay, or an impact resetting. The discovery of stishovite in Tishomingo, indicating exposure to a minimum shock pressure of 8–9 GPa, is consistent with the latter.Stishovite in Tishomingo and chromite included in troilite-daubréelite in IVB irons allows oxygen isotopic composition comparison between these meteorites. Different mass independent oxygen isotopic compositions of IVB irons and Tishomingo indicate genetically distinct parent bodies. By contrast, mass independent Mo isotopic compositions overlap within analytical uncertainties, indicating a similar, carbonaceous chondrite (CC) type genetic heritage. Molybdenum and 183W isotopic data for Chinga and Willow Grove indicate derivation from CC type parent bodies. Willow Grove shares Mo and 183W isotopic compositions with the Ni-rich South Byron Trio (SBT) grouplet and the Milton pallasite. These Ni-rich meteorites likely formed in the same general nebular environment as other CC planetesimals, likely the outer Solar System.Highly siderophile element (HSE) abundances of Willow Grove and Tishomingo are similar to some IVB meteorites, consistent with formation by moderate degrees of fractional crystallization from initial metallic melts with low S and P, and modestly fractionated HSE. The comparable HSE abundances of Tishomingo and Willow Grove to some IVB irons, yet substantially higher Ni concentrations, indicate formation on parent bodies with lower bulk HSE abundances or HSE concentration in proportionally smaller volumes of metal. HSE abundances in Chinga are considerably lower than in IVB irons, highly fractionated, and processes responsible for these remain elusive.For IVB irons and these ungrouped irons, high temperature condensation likely dominated the enrichment and depletion of the refractory and volatile siderophile elements, respectively. Parent body degassing may have also played a role. Relative depletion of volatile siderophile elements is not, however, a universal feature of high-Ni meteorites. The SBT and Milton pallasite are Ni-rich, but less depleted in the more volatile siderophile elements. Nickel enrichment was likely driven by oxidation of Fe metal during parent body accretion or core segregation. Oxidation of the Tishomingo and Willow Grove parent bodies may have occurred at ∼ IW + 1, indicated by relative Mo and W depletions due to metal/water reaction during differentiation. Late-stage reduction, indicated by the presence of Cr-bearing sulfides in Tishomingo and IVB irons, may have resulted from exhaustion of the oxidant.

Barium stable isotopic composition of chondrites and its implication for the Earth

Barium is a refractory and fluid mobile element that is highly incompatible in basaltic systems. The elemental and isotopic compositions of Ba are used to trace fluid processes or sediment recycling during subduction. However, the Ba isotopic composition of primitive meteorites (chondrites), which represents the possible building blocks of terrestrial planets, is presently poorly known. Here, we report high precision Ba isotopic compositions of major types of chondrites using a double-spike method. Chondritic meteorites without clear terrestrial weathering show relatively homogeneous Ba isotopic distributions and have an average δ137/134Ba (the permil deviation of the 137Ba/134Ba ratio from the SRM3104a standard) value of 0.09 ± 0.09‰ (2SD, N = 14). Given the refractory and lithophile behavior of Ba and the limited variations of Ba isotope composition between various chondrite groups, this value can represent the Ba isotopic composition of the bulk Earth and the Bulk Silicate Earth (BSE). It is actually consistent with the present estimate of BSE (0.05 ± 0.06‰, Li et al., 2020; Nan et al., 2022) based on the measurements of mid-ocean ridge basalts and carbonatites. Small Ba isotope variations are observed between carbonaceous chondrite groups where CO and CV show slightly heavier (by 0.09‰) Ba isotopic compositions than CI and CM. Significant light stable Ba isotopes enrichment has previously been documented in calcium, aluminum-rich inclusions (CAIs) in the Allende CV chondrite, and the Ba isotopic differences between CO and CV might result from the various proportions of CAIs based on a mass balance calculation. However, the parent body of CI and CM might have experienced aqueous alteration and secondary carbonates are most likely responsible for their light Ba isotopic signatures.

Spectral and Petrographic Properties of Inclusions in Carbonaceous Chondrites and Comparison with In Situ Images from Asteroid Ryugu

Abstract We imaged a set of carbonaceous chondrites from the CM2, CO3, CV3, and CK4 groups using the qualification model of MasCam, the camera on board the asteroid lander MASCOT, which touched down on asteroid Ryugu in 2018 October. A CI1 meteorite was also imaged but excluded from the analysis due to prominent terrestrial weathering. Following the methods used to image the rock on Ryugu, we placed a total of 14 meteorites approximately 20 cm in front of the camera to achieve a spatial resolution of about 0.2 mm per pixel and illuminated the samples with onboard light-emitting diodes of four different colors in the visible wavelength range. We mapped bright and dark inclusions within the meteorites and derived the inclusion brightness relative to the matrix in the red light, the relative spectral slope of each inclusion, the inclusion size frequency distribution and the matrix volume abundance. We find that the meteorite groups overlap within these parameters, but individual samples, as well as individual inclusions, can have deviating values. Terrestrial weathering appears to have no systematic influence on these parameters. Relating our analysis to the inclusions found in the rock on Ryugu, we find that the spectral parameters of Ryugu’s inclusions fit well in the parameter space of the carbonaceous chondrites. Compared with the most common types of carbonaceous chondrites, Ryugu’s rock has larger inclusions (mean diameter: 0.63 ± 0.91 mm) and a higher upper limit to the matrix abundance (92.4 vol%).

Petrology and classification of A‐9003, A 09535, and Y‐82094: A new type of carbonaceous chondrite

AbstractMost carbonaceous (C) chondrites are classified into eight major groups: CI, CM, CO, CV, CK, CR, CH, and CB. However, some are ungrouped. We studied two such chondrites, Asuka (A)‐9003 and A 09535. The abundance of chondrules and matrix and chondrule sizes in these meteorites are similar to those in ordinary chondrites and unlike any known carbonaceous chondrite group. In contrast, they contain 4–6 vol% of refractory inclusions and have oxygen isotopic compositions within the range of CO and CV chondrites. Therefore, A‐9003 and A 09535 are classified as C chondrites. Petrologic subtypes of A‐9003 and A 09535 are 3.2. All these features closely resemble those of another ungrouped chondrite, Yamato (Y)‐82094, and differ from those of any C chondrites reported by now. A‐9003, A 09535, and Y‐82094 likely represent a new type of C chondrite. We provisionally call them CA chondrite after Asuka in Antarctica. Our study suggests a wider range of formation conditions for C chondrites than currently recorded by the major C chondrite groups.

A new method for determining the petrologic type of unequilibrated ordinary chondrites that can be applied to asteroids

In order to find an additional quantitative way to estimate the petrographic type of unequilibrated ordinary chondrites (UOC), and one that can be used remotely in the study of asteroids, we have analyzed the near-infrared spectra of a suite of UOC observed falls. We obtained spectra from the RELAB database at Brown University and applied several methods for determining the amount of clinopyroxene (CPX) as a percentage of the total pyroxene in the meteorites. The presence of low-Ca CPX has long been known to be characteristic of little-metamorphosed ordinary chondrites. The methods we used were (1) naked-eye determination of the wavelength of the absorption features at ~1 μm and ~2 μm, (2) determination of the wavelengths of these features by fitting polynomial equations, and (3) determining the relative intensities of the CPX and OPX features after isolation by a curve fitting procedure. The measurements were then “calibrated” using data from the literature to obtain values for the amount of CPX in the total pyroxene. We find that there is an empirical relationship between the amount of CPX detected by these methods of spectrum analysis and the petrologic type.Petrologic type=+4.402–0.019×CPX%We explain this empirical relationship (1) as evidence that in pyroxene bearing rocks the spectrum of pyroxene dominates (this has been known in the 1970s), (2) that low-Ca CPX is so abundant in these meteorites (up to 40 vol%) that it is easily detected by reflectance spectroscopy, and (3) compositional effects caused by Ca and Fe in the pyroxenes partially cancel out or are small. We thus have a new method of quantitatively measuring the level of metamorphic alteration experienced by these important meteorites and of assigning them a petrologic type of 3.0 to 3.9. More importantly, unlike existing methods, this can be applied remotely so that chondritic asteroid surfaces (i.e. those of Q and S asteroids) can also be characterized in terms of their metamorphic history. As an example, (433) Eros and (25143) Itokawa were found to be types ~3.5 and ~3.4, respectively. We briefly discuss the implications of this for understanding the history of meteorites and asteroids.

The polymict carbonaceous breccia Aguas Zarcas: A potential analog to samples being returned by the OSIRIS‐REx and Hayabusa2 missions

AbstractOn April 23, 2019, a meteorite fall occurred in Aguas Zarcas, Costa Rica. According to the Meteoritical Bulletin, Aguas Zarcas is a brecciated CM2 chondrite dominated by two lithologies. Our X‐ray computed tomography (XCT) results show many different lithologies. In this paper, we describe the petrographic and mineralogical investigation of five different lithologies of the Aguas Zarcas meteorite. The bulk oxygen isotope compositions of some lithologies were also measured. The Aguas Zarcas meteorite is a breccia at all scales. From two small fragments, we have noted five main lithologies, including (1) Met‐1: a metal‐rich lithology; (2) Met‐2: a second metal‐rich lithology which is distinct from Met‐1; (3) a brecciated CM lithology with clasts of different petrologic subtypes; (4) a C1/2 lithology; and (5) a C1 lithology. The Met‐1 lithology is a new and unique carbonaceous chondrite which bears similarities to CR and CM chondrite groups, but is distinct from both based on oxygen isotope data. Met‐2 also represents a new type of carbonaceous chondrite, but it is more similar to the CM chondrite group, albeit with a very high abundance of metal. We have noted some similarities between the Met‐1 and Met‐2 lithologies and will explore possible genetic relationships. We have also identified a brecciated CM lithology with two primary components: a chondrule‐poor lithology and a chondrule‐rich lithology showing different petrologic subtypes. The other two lithologies, C1 and C1/2, are very altered and possibly related to the CM chondrite group. In this article, we describe all the lithologies in detail and attempt a classification of each in order to understand the origin and the history of formation of the Aguas Zarcas parent body.

Meteoritic amino acids as chemical tracers of parent-body chemistries

ABSTRACT The analysis of the organic matter of meteorites made it possible to identify over 70 amino acids (AA), including 8 of those found in living organisms. However, their relative abundances vary drastically with the type of the carbonaceous chondrite, even for isomers of same chemical formula. In this report, we address the question whether this difference may have its origin in the relative stability of these isomers according to the conditions they experienced when they were formed and after. To this end, we rely on the fact that for most of the species observed so far in the interstellar medium (ISM), the most abundant isomer of a given generic chemical formula is the most stable one (minimum energy principle, MEP). Using quantum density functional theory (DFT) simulations, we investigate the relative stability of the lowest energy isomers of alanine (Ala) and amino butyric acid (ABA) in the neutral, protonated, and zwitterionic structures together with corresponding nitrile precursors. It is shown that β-alanine and γ-ABA are the most stable in a protonated form, whereas α-AA are the most stable in the zwitterionic and nitrile structures. The different composition of the carbonaceous chondrites CIs and CMs could be linked to the chemical context of the aqueous alterations of the parent bodies.