Chondrules, ferromagnesium spherules prevalent in undifferentiated extraterrestrial materials, are the main high-temperature products of the protoplanetary disk. Relict minerals recorded precursor compositions and thermal histories of chondrules, offering critical constraints on the long-debated chondrule heating mechanism. We identified pervasive relict refractory anorthite grains (<= 5 & micro;m) in Al-rich chondrules (bulk Al2O3 >= 10 wt%, ARCs) from pristine carbonaceous chondrites. These grains form rims around relict spinel aggregates or intergrow with high-Ca pyroxene/olivine relics, indicating preferential recycling of anorthite-rich inclusions during outer-disk chondrule heating events over the more abundant melilite-rich ones. The wide occurrence of relict anorthite, which can be readily melted or dissolved in chondrule melts, suggesting that ARCs were most likely formed by one-time crystallization and isolated from subsequent heating events after solidification. Thus, their Al-Mg ages of similar to 2.0-2.5 Ma after CAIs imply that refractory materials were continuously involved over nearly the entire period of outer-disk chondrule formation. Additionally, we infer that a portion of co-formed iron-poor ferromagnesium chondrules must have similarly escaped completely remelting by subsequent intense heating events in the same reservoirs. These findings suggest that the heating events that lead to outer-disk chondrule formation are localized and infrequent, aligning with mechanisms of bow shocks, lightning discharges, and impact jetting but not the large-scale nebular shocks.

Silica polymorphs in meteorites provide critical constraints on crystallization processes associated with thermal activity in the early solar system. A detailed investigation of silica polymorphs in eucrites (the largest group of achondrites) using cathodoluminescence imaging and laser-Raman spectroscopy revealed significant variations in the relative abundance of silica polymorphs. Based on these variations, the eucrites were divided into four "Si-groups" according to their dominant silica phase: Si-0 (cristobalite-dominant eucrites), Si-I (quartz-dominant eucrites), Si-II (quartz and tridymite-dominant eucrites), and Si-III (tridymite-dominant eucrites). In studied eucrites, tridymite and cristobalite form lathy euhedral shapes, while quartz is anhedral, coexistent with opaques and phosphates, suggesting that silica polymorphs were crystallized from different stages and formation processes. We propose a new model that explains the formation pathways of silica minerals in eucrites and accounts for the distinct formation histories represented by each Si-group: tridymite crystallizes from alkali-rich immiscible melts (starting at >= similar to 1060 degrees C), cristobalite crystallizes from quenched melts (similar to 1060 degrees C), and quartz crystallizes from extremely differentiated melts and/or by solid-state transformation from tridymite and cristobalite through interactions with sulfur-rich vapor below similar to 1025 degrees C. This model explains the occurrences of silica polymorphs in eucrites without requiring secondary heating or shock processes.

In this paper, we examine the diverse features of CM (Mighei-type) and related carbonaceous chondrites, including their petrologic classification, secondary heating, brecciation, and we explore anomalous CM-like chondrites. CM chondrites experienced varying degrees of aqueous alteration, resulting in a range of petrologic subtypes from 3.0 to 2.0. The most abundant subtypes are 2.3-2.0, which may reflect melting of significant amounts of ice, resulting in the formation of the heavily altered CM chondrites in the inner regions of the parent body. Additionally, some CM and related chondrites have undergone secondary heating after aqueous alteration. The source of heat for these chondrites is still uncertain, but impacts are the most likely the cause due to the evidence for a short duration of heating. CM chondrites are mainly genomict breccias and contain clasts of various petrologic grade and degree of heating, though some CMs contain xenolithic clasts. Highly recrystallized clasts are particularly important, as they might have formed in the interior, hotter regions of the CM parent body. Subsequently, these clasts may have been mixed with other typical CM lithologies due to impact events. CM chondrite fragments are commonly found in other meteorites, such as HED meteorites and ordinary chondrites. This indicates a widespread distribution of CM chondrite fragments in the main asteroid belt, with incorporation into other meteorites taking place significantly later than chondrule formation. There have been numerous descriptions of anomalous CM or related chondrites. We tentatively classify these anomalous CMs into four categories: highly 16O-rich, medium 16O-rich, an unusual mineral group, and others. However, the processes involved in the formation of these anomalous chondrites and their relationships to the more typical CMs remain unclear, as detailed documentation of most of the anomalous CMs is currently lacking. CM chondrites primarily consist of chondrules, refractory inclusions, opaque minerals, and a matrix material, similar to other C chondrites. The petrographic and bulk chemical features of CMs are most similar to CO chondrites. However, CM and CO chondrites did not originate from a single parent body. CM chondrites provide valuable information about the conditions and processes that operated in the outer region of the early solar system.

The in‐plane rotation method is used to obtain X‐ray random diffraction (XRD) patterns of polished thin sections of 10 CM chondrites. The samples include five intermediately altered CM chondrites with subtypes 2.6–2.3, two heavily altered CM chondrites with subtype 2.0 and three with secondary heating after hydration (Y 980036, Y 980051, and Jbilet Winselwan). These CM chondrites are compared to each other as well as four previously analyzed CM meteorites of subtypes 3.0–2.8 and 2.0. The same thin sections also underwent textural observations and compositional analyses. Unheated CM chondrites display systematic mineralogical changes. As the alteration degree increases from subtypes 3.0–2.0, the presence of olivine and clinoenstatite decreases, while that of serpentines increases. The abundance of tochilinite significantly increases from 2.7 to 2.3 but then decreases from 2.3 to 2.0. Subtype 2.0 consists of relatively more Mg‐rich serpentine than Fe‐rich serpentine (cronstedtite). The XRD identified only Mg‐serpentine from Jbilet Winselwan, suggesting selective decomposition of Fe‐rich serpentine (cronstedtite), while all hydrous minerals in Y 980036 and Y 980051 decomposed. Additionally, all three CM chondrites with secondary heating after hydration show stage II or category B heating by the peak metamorphic temperature of 300–750°C. Compared to previous studies using XRD, the combination of XRD with the textural and compositional analyses using the same polished thin section, avoiding the preparation for powder samples, is a straightforward approach to characterize hydrated chondritic samples. The approach is nondestructive and can be correlated with SEM/EPMA, unlike previous XRD studies that required powdered samples.

Type 3 chondrites are subdivided into 3.0-3.9. Subtype 3.0 chondrites nearly preserve all of their primitive features. Many criteria have been proposed to distinguish such primitive chondrites. Here, we compiled mineral data and reconsider the petrologic classification criteria for subtype 3.0. Chondrites are classified into subtypes by the minor element distribution of olivine and textural and chemical features of Fe-Ni metal. The []Si4O8 and MgO components of feldspar also distinguish subtype 3.0 from subtypes >= 3.1. Other features, such as the occurrence of near pure chromite, are also indicators of subtype 3.0. It is difficult to distinguish between subtypes 3.0 and <= 2.9 based on mineral chemistry. Therefore, we propose the following criteria to distinguish between subtypes 3.0 and <= 2.9. In type 3.0 chondrites, major silicate (olivine, pyroxene, and plagioclase), oxide, metal, and sulfide minerals do not show aqueous alteration features. Melilite, anorthite, and glass show no or mild aqueous alteration features. Subtype 3.0 has not been identified in all chondrite groups. The absence of subtype 3.0 from some groups mainly reflects differences in the degrees of secondary parent body processes among the chondrite groups.

The mechanism of gas-melt interactions and the compositions of precursors are key to understanding the formation of chondrules. To shed light on the two enigmas, we studied the petrography, chemistry, and oxygen isotopes of six Al-rich chondrules (ARCs, five glassy and one plagioclase-bearing) in unequilibrated ordinary chondrites (OCs, petrologic subtype: 3.05). The plagioclase-bearing ARC was also investigated with Al-Mg chronology. Elemental zonation and inter-element correlations in glassy mesostasis of two ARCs indicate the condensation of gaseous Mg, SiO, Fe, and Na onto chondrule melt. The plagioclase-bearing ARC appears to display internal mass-independent oxygen isotope fractionation with delta 18O increasing following the order of mineral crystallization, suggesting partial oxygen isotope exchange with ambient gas during crystallization. Oxygen isotopes of the six ARCs are distributed along a mixing line of slope = 0.99 +/- 0.05, which intersects with calcium-aluminum-rich inclusions (CAIs), consistent with a small portion of OC type IA chondrules, but deviates from other OC ferromagnesium chondrules (FMCs) towards higher delta 17O, suggesting that OC ARCs and some IA chondrules were established by interactions between CAI-like melts and 16O-poor ambient gas, rather than simply remelting solid mixtures of CAI and FMC materials. All six ARCs have unfractionated refractory lithophile element patterns with bulk concentrations ranging from-7 x CI to-15 x CI, indicating- 30-100 % of CAI-like materials in their precursors. Their bulk compositions are linearly evolved toward the Mg: SiO- 3:2 to 2:1 (in atomic) apex, consistent with adding gaseous Mg and SiO to the chondrule bulk via gas-melt interactions. The back-calculated compositions of the recycled CAI-like materials closely overlap with pyroxene-anorthite-rich CAIs, suggesting that extensive interactions between the melt of pyroxene-anorthite-rich CAI-like materials and ambient gas could make OC ARCs. The Al-Mg age of the plagioclase-bearing ARC is-2.2 Ma after CAIs, similar to typical OC FMCs, suggesting that the refractory component arrived at the OC reservoirs in the late stage of the chondrule heating events.

Solar system abundances of the elements, which are determined by spectroscopic measurements of the solar photosphere and laboratory analyses of CI (Ivuna-type) carbonaceous chondrites, are a cornerstone to understand the origin and evolution of planets and other constituents, such as asteroids and comets. Mercury (Hg) is one of the elements whose solar system abundance is still poorly constrained due to no observable lines for Hg in the solar spectrum and large variations of the Hg abundance in CI chondrites caused by mainly terrestrial contamination. Here we determined elemental abundances including Hg for uncontaminated CI-like material from asteroid Ryugu by the Hayabusa2 spacecraft. The new solar system abundance of Hg is 0.907±0.108 atoms/10 6 Si atoms. Our results demonstrate that Hg in bulk silicate Earth originated from the addition of chondritic material after core formation, late sulfide segregation and/or degassing, and volatile elements are depleted in late-accreted materials relative to CI chondrites.

CI chondrites are the most significant extra-terrestrial samples for estimating the composition of primordial materials in the Solar System. However, CIs lose many primary features because of heavy parent body aqueous alteration. However, CI and CI-related Ryugu particles contain small amounts of relict anhydrous minerals, indicating primary occurrences of chondrules and refractory inclusions. In this study, we estimated the primordial abundance of chondrules in CIs from calculations of the bulk major element compositions. The constraints for the calculation were as follows: 1) CI chondrites primarily comprised chondrules, refractory inclusions, opaque minerals, and a matrix similar to other carbonaceous (C) chondrites. 2) The chemical compositions of these components were similar to those of the unaltered C chondrites. 3) The primary matrix composition of the CI was close to the mean bulk composition. 4) The alteration occurred isochemically. We used the mean major elemental compositions of chondrules and refractory inclusions in an almost unaltered chondrite, Y-81020, CO3.05. Our results were within the range of previously reported CI bulk chemical compositions in the case where chondrule abundances are less than or similar to 10 wt%. We also calculated the bulk chemical composition of Tagish Lake, ungrouped C2, which primarily contained less than or similar to 20 wt% chondrules. The CI chondrites and Tagish Lake were formed in the outer Solar System. The low primary abundance of chondrules in CIs is closely related to the formation conditions of chondrules in such regions. We suggest that dust with abundant ice and minor chondrules accreted onto the parent bodies of the CI and Tagish Lake in the outer Solar System. Primordial chondrule abundance is the key to clarifying the physical and chemical conditions and evolution of the early Solar System.

Chondrules and Ca-Al-rich inclusions (CAIs) have been considered characteristic constituents of chondritic meteorites, although the outward transportation of CAIs has been theoretically pointed out. Stardust samples recovered by the Stardust mission from the 81P/Wild2 comet contained chondrule-like objects (CLOs) and refractory inclusions that include CAIs and amoeboid olivine aggregates (AOAs). However, it was not proven that the CLOs, AOAs, and CAIs coexist with fine-grained materials equivalent to chondritic porous interplanetary dust particles (CP IDPs) containing abundant glass with embedded metal and sulfides (GEMS). Here we report on two type II CLOs, containing <90 Mg# in ferromagnesian silicates, enclosed in GEMS-rich CP Antarctic micrometeorites (AMMs) (CP IDPs that reached the surface of the Earth) and one igneous object rich in kosmochloric (Ko-rich: NaCrSi2O6-rich) high-Ca pyroxene and Fe-bearing olivine (KOOL) that is enclosed in a CP IDP. KOOL grains have also been found in Stardust samples and CP IDPs. These three igneous objects are embedded in fine-grained matrices that do not show any evidence of aqueous alteration. The low Mg# and elevated Delta O-17 of olivine and pyroxene in these CLOs and the KOOL grain are consistent with previously studied CLOs from comet 81P/Wild 2 and a giant cluster IDP. These results support the view that CP IDP- and CP AMM-like materials constitute samples from comets or comet-like icy bodies. The CLOs were formed in oxidizing environment beyond the snow line and then transferred to the comet-forming region. In contrast, a spinel-hibonite (SHIB) fragment found in an AMM experienced aqueous alteration of its rim. The SHIB fragment contains ultrarefractory oxides and refractory metal nuggets and has a Mg-26 excess like typical meteoritic CAIs. The mineralogy of the fine-grained matrix is very similar to CP IDPs and CP AMMs. However, because "GEMS" in the matrix of the SHIB fragment-bearing AMM lacks Fe-Ni metal and amorphous silicate in it contains Fe, it is clear that the matrix weakly experienced aqueous alteration. Olivine / (Olivine + low-Ca pyroxene) ratios in the matrices of the four samples range from 0.4 to 0.6, which are comparable with those of anhydrous CP IDPs and CP MMs (around 0.5), and those of P- and D-type asteroids and Jupiter-family comets (around 0.5).

AbstractSilica polymorphs occur under various pressures and temperature conditions, and their characteristics can be used to better understand the complex metamorphic history of planetary materials. Here, we conducted isothermal heating experiments of silica polymorphs in basaltic eucrites to assess their formation and stability. We revealed that each silica polymorph exhibits different metamorphic responses: (1) Quartz recrystallizes into cristobalite when heated at ≥ 1040 °C. (2) Monoclinic (MC) tridymite recrystallizes into no other polymorphs when heated at ≤ 1070 °C. (3) Silica glass recrystallizes into quartz when heated at 900–1010 °C, and recrystallize into cristobalite when heated at ≥ 1040 °C. These results suggest that MC tridymite in eucrites does not recrystallize into other polymorphs during the reheating events, nor does it recrystallize from other silica phases below the solidus temperature of eucrite (~ 1060 °C). Additionally, we found that pseudo-orthorhombic (PO) tridymite crystallizes from quenched melts in the samples heated at ≥ 1070 °C. Previously, cristobalite has been considered as the initial silica phase, which crystallizes from eucritic magma. Our findings suggest that the first crystallizing silica minerals may not always be cristobalite. These require a reconsideration of the formation process of silica minerals in eucrites.

Parent bodies of C-type asteroids may have brought key volatile and organic-rich compounds to the terrestrial planets in the early stages of the Solar System. At the end of 2020, the JAXA Hayabusa2 mission successfully returned samples from Ryugu, providing access to a primitive matter that has not suffered terrestrial alteration. Here we report the discovery of a peculiar class of grains, up to a few hundreds of micrometres in size, that have a hydrated ammonium-magnesium-phosphorus (HAMP)-rich composition. Their specific chemical and physical properties point towards an origin in the outer Solar System, beyond most snow lines, and their preservation along Ryugu history. These phosphorus-rich grains, embedded within an organic-rich phyllosilicate matrix, may have played a major role when immersed in primitive terrestrial water reservoirs. In particular, in contrast to poorly soluble calcium-rich phosphates, HAMP grains favour the release of phosphorus-rich and nitrogen-rich ionic species, to enter chemical reactions. HAMP grains may have thus critically contributed to the reaction pathways of organic matter towards a biochemical evolution. Hydrated ammonium-magnesium-phosphorus-rich grains have been discovered in Ryugu samples. Embedded within an organic-rich phyllosilicate matrix, they may have been a key source of phosphorus and nitrogen in early terrestrial water reservoirs.

Ryugu is the C-type asteroid from which material was brought to Earth by the Hayabusa2 mission. A number of individual grains and fine-grained samples analysed so far for noble gases have indicated that solar wind and planetary (known as P1) noble gases are present in Ryugu samples with concentrations higher than those observed in CIs, suggesting the former to be more primitive compared to the latter. Here we present results of analyses of three fine-grained samples from Ryugu, in one of which Xe concentration is an order of magnitude higher than determined so far in other samples from Ryugu. Isotopically, this Xe resembles P1, but with a much stronger isotopic fractionation relative to solar wind and significantly lower 36Ar/132Xe ratio than in P1. This previously unknown primordial noble gas component (here termed P7) provides clues to constrain how the solar composition was fractionated to form the planetary components. Ryugu is more primitive than carbonaceous chondrites, according to elevated noble gas concentrations. Elevated Xe and its isotopic composition further provide constraints on fractionation of the solar composition to form the early planetary components.

Although CI chondrites are susceptible to terrestrial weathering on Earth, the specific processes are unknown. To elucidate the weathering mechanism, we conduct a laboratory experiment using pristine particles from asteroid Ryugu. Air-exposed particles predominantly develop small-sized euhedral Ca-S-rich grains (0.5-1 mu m) on the particle surface and along open cracks. Both transmission electron microscopy and synchrotron-based computed tomography combined with XRD reveal that the grains are hydrous Ca-sulfate. Notably, this phase does not form in vacuum- or nitrogen-stored particles, suggesting this result is due to laboratory weathering. We also compare the Orgueil CI chondrite with the altered Ryugu particles. Due to the weathering of pyrrhotite and dolomite, Orgueil contains a significant amount of gypsum and ferrihydrite. We suggest that mineralogical changes due to terrestrial weathering of particles returned directly from asteroid occur even after a short-time air exposure. Consequently, conducting prompt analyses and ensuring proper storage conditions are crucial, especially to preserve the primordial features of organics and volatiles.

Micrometeorites, a possible major source of Earth’s water, are thought to form from explosive dispersal of hydrated chondritic materials during impact events on their parental asteroids. However, this provenance and formation mechanism have yet to be directly confirmed using asteroid returned samples. Here, we report evidence of mild shock metamorphism in the surface particles of asteroid Ryugu based on electron microscopy. All particles are dominated by phyllosilicates but lack dehydration textures, which are indicative of shock-heating temperatures below ~500 °C. Microfault-like textures associated with extensively shock-deformed framboidal magnetites and a high-pressure polymorph of Fe–Cr–sulfide have been identified. These findings indicate that the average peak pressure was ~2 GPa. The vast majority of ejecta formed during impact on Ryugu-like asteroids would be hydrated materials, larger than a millimetre, originating far from the impact point. These characteristics are inconsistent with current micrometeorite production models, and consequently, a new formation mechanism is required.

The delivery of water to the inner Solar System, including Earth, is still a debated topic. A preferential role for hydrated asteroids in this process is supported by isotopic measurements. Carbonaceous chondrite (CC) meteorites represent our main source of information about these volatile-rich asteroids. However, the destruction of weaker materials during atmospheric entry creates a bias in our CC data. The return of surface materials from the C-type asteroid 162173 Ryugu by the Hayabusa2 spacecraft provides a unique opportunity to study high-porosity, low-density, primitive materials, unrepresented in the meteorite record. We measured the bulk oxygen isotope composition from four Ryugu particles and show that they most closely resemble the rare CI (CC Ivuna-type) chondrites, but with some differences that we attribute to the terrestrial contamination of the CI meteorites. We suggest that CI-related material is widespread among carbonaceous asteroids and a more important source of Earth’s water and other volatiles than its limited presence in our meteoritic collection indicates.

Samples of the carbonaceous asteroid Ryugu were brought to Earth by the Hayabusa2 spacecraft. We analyzed 17 Ryugu samples measuring 1 to 8 millimeters. Carbon dioxide-bearing water inclusions are present within a pyrrhotite crystal, indicating that Ryugu's parent asteroid formed in the outer Solar System. The samples contain low abundances of materials that formed at high temperatures, such as chondrules and calcium- and aluminum-rich inclusions. The samples are rich in phyllosilicates and carbonates, which formed through aqueous alteration reactions at low temperature, high pH, and water/rock ratios of <1 (by mass). Less altered fragments contain olivine, pyroxene, amorphous silicates, calcite, and phosphide. Numerical simulations, based on the mineralogical and physical properties of the samples, indicate that Ryugu's parent body formed ~2 million years after the beginning of Solar System formation.

NWA 8785 is a remarkable EL3 chondrite with a high abundance (similar to 34 vol%) of an Fe-rich matrix. This is the highest matrix abundance known among enstatite chondrites (ECs) and more similar to the matrix abundances in some carbonaceous and Rumuruti chondrites. X-ray diffraction and TEM data indicate that the fine-grained portion of the NWA 8785 matrix consists of nanoscale magnetite mixed with a noncrystalline silicate material and submicron-sized enstatite and plagioclase grains. This is the first report of magnetite nanoparticles in an EL3. The Si content of the metal (0.7 wt%), presence of ferroan alabandite, and its O isotopic composition indicate NWA 8785 is EL3-related. Having more abundant matrix than in other ECs, and that the matrix is rich in magnetite nanoparticles, which are not present in any other EC, suggest classification as an EL3 anomalous. Although we cannot completely exclude any of the mechanisms or environments for formation of the magnetite, we find a secondary origin to be the most compelling. We suggest that the magnetite formed due to hydrothermal activity in the meteorite parent body. Although ECs are relatively dry and likely formed within the nebular snow line, ices may have drifted inward from just beyond the snow line to the region where the EL chondrites were accreting, or more likely the snow line migrated inward during the early evolution of the solar system. This may have resulted in the condensation of ices and provided an ice-rich region for accretion of the EL3 parent body. Thus, the EL3 parent body may have had hydrothermal activity and if Earth formed near the EC accretion zone, similar bodies may have contributed to the Earth's water supply. NWA 8785 greatly extends the range of known characteristics of ECs and EC parent body processes.