Petrologic Subtype Research Articles

The secondary classification of unequilibrated chondrites

AbstractThe multiplication of decimal petrologic schemes for different or the same chondrite groups evinces a lack of unified guiding principle in the secondary classification of type 1–3 chondrites. We show that the current OC, R and CO classifications can be a posteriori unified, with only minor reclassifications, if the decimal part of the subtype is defined as the ratio m = FaI/FaII of the mean fayalite contents of type I and type II chondrules, rounded to the nearest tenth (with adaptations from Cr systematics for the lowest subtypes following the past literature). This parameter is more efficiently evaluable than the oft‐used relative standard deviation of fayalite contents and defines a general metamorphic scale from M0.0 to M1, where the suffixed number is the rounded m. Type 3 chondrites thus span the range M0.0–M0.9 (i.e. subtypes 3.0–3.9) and M1 designates type 4. Corresponding applications are then proposed for other chondrite groups (with, e.g., CV secondary classification reduced to essentially three grades from M0.0 to M0.2, that is, subtypes 3.0–3.2). Known type 1 and 2 chondrites are at M0.0 (i.e. the metamorphic grade of type 3.0 chondrites), even so‐called “CY” chondrites, since our metamorphic scale is insensitive to brief heating. Independently, we define an aqueous alteration scale from A0.0 to A1.0, where the suffixed number is the (rounded) phyllosilicate fraction (PSF). For CM and CR chondrites, the alteration degrees can be characterized in terms of the thin‐section‐based criteria of previous schemes which are thus incorporated in the present framework, if in a coarser, but hereby more robust form. We propose their corresponding petrologic subtype to be 3‐PSF, rounded to the nearest tenth (so that type 1 would correspond to subtypes 2.0 and 2.1). Since nonzero alteration and metamorphic degrees remain mutually exclusive at the level of precision chosen, a single petrologic subtype ≈3+m‐PSF indeed remains a good descriptor of secondary processes for all unequilibrated chondrites, obviating the explicit mention of our separate scales unless finer subdivisions are adopted for the most primitive chondrites.

Chondrule sizes within the CM carbonaceous chondrites and measurement methodologies

AbstractThe sizes of chondrules are a valuable tool for understanding relationships between meteorite groups and the affinity of ungrouped chondrites, documenting temporal/spatial variability in the solar nebula, and exploring the effects of parent body processing. Many of the recently reported sizes of chondrules within the CM carbonaceous chondrites differ significantly from the established literature average and are more closely comparable to those of chondrules within CO chondrites. Here, we report an updated analysis of chondrule dimensions within the CM group based on data from 1937 chondrules, obtained across a suite of CM lithologies ranging from petrologic subtypes CM2.2 to CM2.7. Our revised average CM chondrule size is 194 μm. Among the samples examined, a relationship was observed between petrologic subtype and chondrule size such that chondrule long‐axis lengths are greater in the more highly aqueously altered lithologies. These findings suggest a greater similarity between the CM and CO chondrites than previously thought and support arguments for a genetic link between the two groups (i.e., the CM‐CO clan). Using the 2‐D and 3‐D data gathered, we also apply numerous stereological corrections to examine their usefulness in correcting 2‐D chondrule measurements within the CM chondrites. Alongside this analysis, we present the details of a standardized methodology for 2‐D chondrule size measurement to facilitate more reliable inter‐study comparisons.

Forging inner-disk Al-rich chondrules by interactions of CAI-like melt and ambient gas

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 δ18O 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 δ17O, 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 × CI to ∼15 × 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.

Identification of a primordial high D/H component in the matrix of unequilibrated ordinary chondrites

Deuterium to hydrogen isotope ratios in unequilibrated ordinary chondrites (UOCs) which have undergone little-to-no thermal metamorphism pose an interesting problem when looking at water in the early Solar System. Bulk chondrite studies have shown that UOCs of the lowest subtypes have D/H ratios as high as comets from the outer Solar System, which, along with bulk UOC water abundances, decrease with thermal metamorphism. Since bulk UOC analyses represent a complex mixture of organic and hydrated phases, it is not clear what phase(s) is responsible for the high bulk D/H values. In this study, we report in situ secondary ion mass spectrometry (SIMS) measurements of the H isotope composition of the fine-grained matrix of UOCs with petrological subtypes ranging from 3.00 to 3.9. We find that for matrix areas in UOCs of petrologic subtype ≥3.2, correlations between D-rich organic material and D-poor phyllosilicates give relatively D-poor intrinsic water isotopic compositions, with δD values between −320 ± 91 ‰ and −71 ± 71 ‰, which are inherited from parent body accretion. Therefore, we conclude that OC parent bodies accreted D-poor water ice that had an H isotopic composition similar to that of CM and CV chondrite parent bodies. We find that matrix in UOCs of the lowest subtypes (Semarkona, Bishunpur, and Ngawi) show similar water and organic H isotope compositions to higher type UOCs. Our in situ analyses also show that matrix areas in these pristine UOCs contain a third, thus far unidentified, component that carries the high D/H signature, with δD values up to ∼6000 ‰. We propose that this component is pristine amorphous silicates preserved from the molecular cloud or early protoplanetary disc that is extremely sensitive to thermal and aqueous alteration on asteroidal parent bodies.

Brecciation at the grain scale within the lithologies of the Winchcombe Mighei‐like carbonaceous chondrite

AbstractThe Mighei‐like carbonaceous (CM) chondrites have been altered to various extents by water–rock reactions on their parent asteroid(s). This aqueous processing has destroyed much of the primary mineralogy of these meteorites, and the degree of alteration is highly heterogeneous at both the macroscale and nanoscale. Many CM meteorites are also heavily brecciated juxtaposing clasts with different alteration histories. Here we present results from the fine‐grained team consortium study of the Winchcombe meteorite, a recent CM chondrite fall that is a breccia and contains eight discrete lithologies that span a range of petrologic subtypes (CM2.0–2.6) that are suspended in a cataclastic matrix. Coordinated multitechnique, multiscale analyses of this breccia reveal substantial heterogeneity in the extent of alteration, even in highly aqueously processed lithologies. Some lithologies exhibit the full range and can comprise nearly unaltered coarse‐grained primary components that are found directly alongside other coarse‐grained components that have experienced complete pseudomorphic replacement by secondary minerals. The preservation of the complete alteration sequence and pseudomorph textures showing tochilinite–cronstedtite intergrowths are replacing carbonates suggest that CMs may be initially more carbonate rich than previously thought. This heterogeneity in aqueous alteration extent is likely due to a combination of microscale variability in permeability and water/rock ratio generating local microenvironments as has been established previously. Nevertheless, some of the disequilibrium mineral assemblages observed, such as hydrous minerals juxtaposed with surviving phases that are typically more fluid susceptible, can only be reconciled by multiple generations of alteration, disruption, and reaccretion of the CM parent body at the grain scale.

Bulk mineralogy, water abundance, and hydrogen isotope composition of unequilibrated ordinary chondrites

AbstractThe origin and transport of water in the early Solar System is an important topic in both astrophysics and planetary science, with applications to protosolar disk evolution, planetary formation, and astrobiology. Of particular interest for understanding primordial water transport are the unequilibrated ordinary chondrites (UOCs), which have been affected by very limited alteration since their formation. Using X‐ray diffraction and isotope ratio mass spectrometry, we determined the bulk mineralogy, H2O content, and D/H ratios of 21 UOCs spanning from petrologic subtypes 3.00–3.9. The studied UOC falls of the lowest subtypes contain approximately 1 wt% H2O, and water abundance globally decreases with increasing thermal metamorphism. In addition, UOC falls of the lowest subtypes have elevated D/H ratios as high as those determined for some outer Solar System comets. This does not easily fit with existing models of water in the protoplanetary disk, which suggest D/H ratios were low in the warm inner Solar System and increased radially. These new analyses confirm that OC parent bodies accreted a D‐rich component, possibly originating from either the outer protosolar nebula or from injection of molecular cloud streamers. The sharp decrease of D/H ratios with increasing metamorphism suggests that the phase(s) hosting this D‐rich component is readily destroyed through thermal alteration.

Assessment of petrologic subtypes, subgroups, and pairing within CV chondrites in the US Antarctic meteorite collection

AbstractCarbonaceous chondrites of the Vigarano group (CV) are primitive (nearly un‐metamorphosed) meteorites that provide a wealth of information about the early solar system, including constraints on chondrule formation, origin of calcium‐aluminum inclusions, stability of organic compounds, and redox conditions. The US Antarctic meteorite collection contains 119 CV samples from 15 dense collection areas (DCAs) from the TransAntarctic Mountains; these samples have been assigned a preliminary classification as CVs, but not to the subgroups oxidized A, oxidized B, and reduced. Furthermore, variation in petrologic grade can be determined non‐destructively using Raman spectroscopy. To update the classification of both subgroups and petrologic types in the collection, we have acquired magnetic susceptibility, metal and sulfide compositions, and Raman spectra. Overall, there are 55 oxidized A samples, 18 oxidized B samples, and 46 reduced samples. Several of the CVs are quite primitive (Lewis Cliffs Ice Tongue and MacAlpine Hills) but are also very small. Multiple pairing groups have been identified in the Miller Range (MIL), Queen Alexandra Range, and Larkman Nunatak DCAs, including all of the subgroups. In MIL 090981, there is evidence for multiple lithologies. We make suggested updates for all the samples, knowing that this information will help to better guide researchers interested in studying the CV chondrites in the US Antarctic meteorite collection.

High precision 26Al-26Mg chronology of chondrules in unequilibrated ordinary chondrites: Evidence for restricted formation ages

Chondrules in ordinary chondrites are considered to form in high density environments, likely related to the evolution of protoplanets and large planetesimals. In order to determine the timing of their formation at high time resolution (≤0.1 Ma), we conducted high precision Al-Mg chronology of 17 porphyritic chondrules from 6 different unequilibrated ordinary chondrites (UOCs) of low petrologic subtypes (3.00–3.05). Detailed petrology, mineralogy, and oxygen isotope ratios of individual chondrules were also obtained that include 10 additional chondrules without Al-Mg ages. Seventeen chondrules for Al-Mg chronology consist of 14 chondrules with plagioclase (An1-An87) and three chondrules with Na-rich glassy mesostasis, all of which have high 27Al/24Mg ratios (30–3000). The inferred initial (26Al/27Al)0 ratios range between (6.5 ± 0.6) × 10–6 to (9.5 ± 1.0) × 10–6, corresponding to chondrule formation ages of 1.74 ± 0.12/0.11 Ma to 2.13 ± 0.09 Ma after CAIs, which have a canonical (26Al/27Al)0 ratio of 5.25 × 10–5. Six albite-bearing chondrules (An<30) show a much more restricted ages range, spanning between 2.00 ± 0.11/0.10 Ma and 2.07 ± 0.11/0.10 Ma. Including 14 anorthite-bearing chondrules studied previously, chondrules in ordinary chondrites have a restricted range of formation ages from 1.8 Ma to 2.2. Ma after CAIs.Based on the newly acquired oxygen isotope data and previous high precision studies, chondrules in L and LL chondrites do not show systematic difference in their δ18O and δ17O signatures. Majority of plagioclase-bearing chondrules studied for Al-Mg chronology show similar oxygen isotope ratios to those of glass-bearing chondrules. There is no obvious difference in Al-Mg ages of chondrules between L and LL chondrites. Thus, chondrules in L and LL chondrites would have formed in common environments and processes, though they accreted to two separate parent bodies by 2.2 Ma after CAIs, which timing is consistent with the proposed thermal model for ordinary chondrite parent bodies. Onset of chondrule formation at 1.8 Ma after CAIs may be caused by the delay of Jupiter formation or the formation of protoplanets in ordinary chondrite chondrule forming regions if chondrules formed by large scale disk shock or impact jetting of protoplanets. Alternatively, early formed chondrules would not be preserved before 1.8 Ma if chondrules formed by the impacts of molten planetesimals.

Plagioclase alteration and equilibration in ordinary chondrites: Metasomatism during thermal metamorphism

In ordinary chondrites (OCs), feldspar is present both in chondrules as a primary, igneous phase, and as a secondary phase that results from crystallization of chondrule mesostasis glass during thermal metamorphism. To further understand the chemical and physical conditions prevailing during thermal metamorphism in OCs, we conducted a study of feldspar microtextures and compositions within chondrules, focusing on alteration and equilibration features. We included OCs representing the full metamorphic sequence (petrologic types 3–6) and all OC groups (H, L and LL). Our observations show that primary calcic plagioclase alters to sodalite, scapolite, and nepheline in petrologic types 3.2–3.9, and to albite in types 3.6–5. Plagioclase also develops alteration features such as zoning, micropores, and alteration lamellae in types 3–4. Sodic plagioclase is present in minor amounts as a primary phase, but also forms from the crystallization of chondrule mesostasis glass (types 3.2–3.9), and predominantly through albitization reactions in calcic plagioclase (types 3.6–5). K-feldspar occurs in albite in types 3.6–6 as fine-scale exsolution lamellae and as larger patches.We combine these observations into an overall model of metasomatism during thermal metamorphism in OCs. Hydrous alteration during prograde metamorphism results in most of the alteration and equilibration features we observe in plagioclase. During retrograde metamorphism, high temperature, short duration infiltration of anhydrous, alkali- and halogen-bearing fluids causes incorporation of K into plagioclase that subsequently exsolves. Overall, we show that evidence of metasomatism is present throughout the metamorphic sequence in all the OCs, and thus was a ubiquitous process on all OC parent bodies. Recognition of the effects of fluid activity in OCs of even the lowest petrologic subtypes has important consequences for radioisotope chronometers, such as Al-Mg and I-Xe, that rely on the integrity of phases such as plagioclase and feldspathic mesostasis glass which are highly susceptible to alteration. Furthermore, the presence of aqueous alteration features in OCs implies that the non-carbonaceous chondrite isotopic reservoir must have also had ices and that models of protoplanetary disk evolution must also include the presence of ices in the inner solar system.

Tracing the earliest stages of hydrothermal alteration on the CM chondrite parent body

AbstractThe CM carbonaceous chondrites are an important resource in our efforts to understand the role of volatiles in the formation of planetary systems. We report the bulk mineralogy, water abundance, and infrared (IR) reflectance spectra of the CM chondrites LaPaz Icefield (LAP) 04514, LAP 04796, LAP 04565, and LAP 02333. They contain abundant Fe‐ and Mg‐rich serpentines (~70–80 vol%), and based on their phyllosilicate fractions, we classify LAP 04514, LAP 04796, and LAP 04565 as petrologic subtype 1.6 and LAP 02333 as 1.4. This is consistent with estimated water abundances of 9.9 (±1.1) wt% for LAP 04796, 10.4 (±0.1) wt% for LAP 04565, and 11.5 (±0.5) wt% for LAP 02333. However, LAP 04514 contains less water (8.8 ± 0.3 wt%), has a shallower 3 µm band depth, and lacks tochilinite having experienced posthydration temperatures of ~300–400 °C. We conclude that LAP 04514, LAP 04796, and LAP 04565 are among the least altered CM chondrites, which retain primitive features from the initial building blocks of the CM parent body. Finally, we use the IR spectral features of LAP 04514, LAP 04796, and LAP 04565 to identify C‐complex asteroid surfaces that record mild levels of hydration.

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.

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.

Formation of metallic-Cu-bearing mineral assemblages in type-3 ordinary and CO chondrites

Abstract Studies of the new growth and re-distribution of Cu-rich phases in chondrites of different petrologic subtypes can potentially provide insights into post-accretionary parent-body processes. We present a systematic study of the distribution of Cu-rich phases and metallic Cu in Ornans-like carbonaceous chondrites (CO3) that underwent little aqueous alteration or shock (most with shock stages of S1) but exhibit a range of thermal metamorphism (subtype 3.0–3.7). A comparison to ordinary chondrites (OCs), which have undergone a larger range of shock levels, allows us to constrain the relative roles of radiogenic and shock heating in the origin of Cu distribution in chondrites. We found that the Cu content of Ni-rich metal and calculated bulk Cu content of CO3 chondrites (based on mass-balance calculations) show an increase from CO3.0 to CO3.2 chondrites. We speculate that some unidentified phases in the matrix account for a significant portion (nearly ~100 ppm) of the Cu budget in bulk samples of CO3.0 chondrites, while Ni-rich metal is the main Cu-carrier for CO3.2–3.7 chondrites. Within CO3.2–3.7 chondrites, Cu and Ni contents of Ni-rich metal are positively correlated, showing a systematic decrease from lower to higher subtype (~0.41 wt% Cu and ~45.0 wt% Ni in CO3.2 Kainsaz; ~0.28 wt% Cu and ~38.8 wt% Ni in CO3.7 Isna). Metallic Cu grains were found in every sample of CO3.2–3.7 chondrites, but not in any CO3.0–3.1 chondrites. Metallic Cu is: (1) present at metallic-Fe-Ni-pyrrhotite interfaces; (2) associated with fine irregular pyrrhotite grains in Ni-rich-metal-pyrrhotite nodules; (3) associated with fizzed pyrrhotite (fine-grained mixtures of irregularly shaped metal grains surrounded by pyrrhotite); (4) present at the edges of metallic Fe-Ni grains; and (5) present as isolated grains. In some metallic-Cu-bearing mineral assemblages, pyrrhotite has higher Cu concentrations than adjacent Ni-rich metal and shows a drop in Cu concentration at the interface between metallic Cu and Cu-rich pyrrhotite. This implies that the precipitation of metallic Cu grains could be related to the local Cu enrichment of pyrrhotite. We consider that radiogenic heating is mainly responsible for the formation of opaque phases in CO chondrites based on the relatively slow metallographic cooling rate (~0.1–5 °C/Ma), the increasing uniformity of Ni contents in Ni-rich metal with increasing CO subtype (44.3 ± 17.3 wt% in CO3.00 to 38.8 ± 3.4 wt% in CO3.7 chondrite), and the relatively narrow range of pyrrhotite metal/sulfur ratios (~0.976–0.999). Metal/sulfur ratios of pyrrhotite grains in most CO3.2–3.7 chondrites (mean = ~0.986–0.997; except Lancé) are slightly higher than those in CO3.0–3.1 chondrites (mean = ~0.981–0.987; except Y-81020), possibly indicative of a release and re-mobilization of sulfur during progressive heating as previously reported for type-3 chondrites. In this regard, we suggest most metallic Cu grains in CO3 chondrites may have precipitated from Cu-rich pyrrhotite due to sulfidation of Fe-Ni metal during parent-body thermal metamorphism. Locally, a few metallic Cu grains associated with fizzed pyrrhotite could have formed during transient shock-heating. Both thermal and shock metamorphism could be responsible for the formation of metallic Cu. Although the systematic decrease in the Ni contents of Ni-rich metal from subtype-3.2 to subtype-3.8 also occurs in OCs, the average Cu contents of Ni-rich metal grains are indistinguishable among type-3 OCs of different subtypes. The paucity of metallic Cu in weakly shocked type-3 OCs could be related to: (1) the relatively low-bulk Cu contents of OCs, and/or (2) the relatively rapid metallographic cooling rates at &amp;lt;500–600 °C (~1–10 °C/Ma for LL chondrites), possibly resulting from early disturbance of OC parent bodies. The intergrowth of metallic Cu and irregular pyrrhotite more commonly occurs in shocked type-4 to type-6 OCs than in CO3 chondrites. This could be due to S in type-4 to type-6 OCs being more mobilized due to shock heating than in unshocked CO3 chondrites. We predict that some other groups of carbonaceous chondrites (e.g., CI and CM) are less likely to produce metallic Cu due to the: (1) relatively low amount of metallic Fe-Ni; (2) relatively low parent-body temperatures of ~100–300 °C; (3) high mobility of Cu in solution for aqueously altered samples; and (4) the short heating duration for metamorphosed samples.

The alteration history of the CY chondrites, investigated through analysis of a new member: Dhofar 1988

We provide the first detailed analysis of the carbonaceous chondrite Dhofar (Dho) 1988. This meteorite find was recovered in 2011 from the Zufar desert region of Oman and initially classified as a C2 ungrouped chondrite. Dho 1988 is a monomict breccia composed of millimetre-sized clasts, between which large (∼50–250 µm) intermixed sulphide-Ca-carbonate veins formed. It has high sulphide abundances (∼14 vol%), medium-sized chondrules (avg. 530 µm, N = 33), relatively low chondrule/CAI abundances (<20 area%), a heavy bulk O-isotope composition (δ17O = 9.12‰, δ18O = 19.46‰) and an aqueously altered and then dehydrated alteration history. These characteristics are consistent with the newly defined Yamato-type (CY) carbonaceous chondrite group, suggesting this meteorite should be reclassified as a CY chondrite.Dho 1988 experienced advanced aqueous alteration [petrologic subtype 1.3 in the scheme of Howard et al. (2015)]. Alteration style and extent are similar to the CM chondrite group, with the matrix having been replaced by tochilinite-cronstedtite intergrowths and chondrules progressively pseudomorphed by phyllosilicates, sulphides and in one instance Ca-carbonates. However, departures from CM-like alteration include the replacement of chondrule cores with Al-rich, Na-saponite and upon which Cr-spinel and Mg-ilmenite grains precipitated. These late-stage aqueous alteration features are common among the CY chondrites. Fractures in Dho 1988 that are infilled by phyllosilicates, sulphides and carbonates attest to post-brecciation aqueous alteration. However, whether aqueous alteration was also active prior to brecciation remains unclear. Veins are polymineralic with a layered structure, allowing their relative chronology to be reconstructed: intermixed phyllosilicate-sulphide growth transitioned to sulphide-carbonate deposition. We estimate temperatures during aqueous alteration to have been between 110 °C < T < 160 °C, based on the co-formation of Na-saponite and tochilinite.Dho 1988 was later overprinted by thermal metamorphism. Peak temperatures are estimated between 700 °C and 770 °C, based on the thermal decomposition of phyllosilicates (both serpentine and saponite) combined with the survival of calcite. As temperatures rose during metamorphism the thermal decomposition of pyrrhotite produced troilite. Sulphur gas was liberated in this reaction and flowed through the chondrite reacting with magnetite (previously formed during aqueous alteration) to form a second generation of troilite grains. The presence of both troilite and Ni-rich metal in Dho 1988 (and other CY chondrites) demonstrate that conditions were constrained at the iron-troilite buffer.

New constraints from 26Al-26Mg chronology of anorthite bearing chondrules in unequilibrated ordinary chondrites

26Al-26Mg ages were determined for 14 anorthite-bearing chondrules from five different unequilibrated ordinary chondrites (UOCs) with low petrologic subtypes (3.00–3.05). In addition, oxygen three isotopes of these chondrules were also measured. The selected chondrules are highly depleted in alkali elements, and anorthite is the only mesostasis phase, though they show a range of mafic mineral compositions (Mg# 76–97 mole%) that are representative of chondrules in UOCs. The mean Δ17O values in these chondrules range from −0.44 ± 0.23‰ to 0.49 ± 0.15‰, in good agreement with previous studies of plagioclase-bearing chondrules from UOCs. Anorthite in all chondrules exhibit resolvable excess 26Mg (>1.0 ± 0.4‰). Their inferred (27Al/26Al)0 range from (6.3 ± 0.7) × 10−6 to (8.9 ± 0.3) × 10−6 corresponding to a timescale for chondrule formation of 1.8 ± 0.04 Ma to 2.16 ± 0.12/0.11 Ma after CAIs using a canonical (27Al/26Al)0 value of 5.25 × 10−5. The ages from six chondrules in LL chondrites are restricted to between 1.8 Ma and 1.9 Ma, whereas eight chondrules in L chondrites show ages from 1.8 Ma to 2.2 Ma, including three chondrules at ∼2.0 Ma and two chondrules at ∼2.15 Ma.The inferred chondrule formation ages from this study are at the peak of those previously determined for UOC chondrules, though with much shorter durations. This is potentially due to the time difference between formation of anorthite-bearing chondrules and typical UOC chondrules with alkali-rich compositions. Alternatively, younger chondrules ages in previous studies could have been the result of disturbance to the Al-Mg system in glassy mesostasis even at the low degree of thermal metamorphism in the parent bodies. Nevertheless, the high precision ages from this study (with uncertainties from 0.04 Ma to 0.15 Ma) indicate that there was potentially more than one chondrule forming event represented in the studied population. Considering data from LL chondrites only, the restricted duration (≤0.1 Ma) of chondrule formation ages suggests an origin in high density environments that subsequently lead to parent body formation. However, the unusually low alkali contents of the studied chondrules compared to common alkali-rich chondrules could also represent earlier chondrule formation events under relatively lower dust densities in the disk. Major chondrule forming events for UOCs might have postdated or concurrent with the younger anorthite-bearing chondrule formation at 2.15 Ma after CAIs, which are very close to the timing of accretion of ordinary chondrite parent bodies that are expected from thermal evolution of ordinary chondrite parent bodies.

Distinguishing relative aqueous alteration and heating among CM chondrites with IR spectroscopy

Using infrared (IR) spectroscopy of thin sections, we characterize the relative degree of aqueous alteration and subsequent heating of a suite of CM chondrites to document spectral indicators of these processes that can contextualize observations of carbonaceous asteroids. We find that the progressive aqueous alteration of CMs manifests in two spectral regions. The low-wavenumber region (1200–400 cm−1; 8–25 μm) records the increasing proportion of Mg-Fe phyllosilicates relative to anhydrous silicates as aqueous alteration proceeds, with a highly correlated shift of the Christiansen feature (CF) to lower wavenumber and the Si-O bending band minimum to higher wavenumber, and an increase in depth of the Mg-OH band (~625 cm−1). The strongest correlation (R2 = 0.90) with petrologic subtype is the distance between the CF and Si-O stretching band minimum, which predicts the petrologic subtype of the sample to within 0.1. The high-wavenumber region (4000–2500 cm−1, ≤3.33 μm) probes the variation in abundance and composition of Mg-Fe serpentine and tochilinite among the altered CMs. All moderately to highly altered CMs (≤2.3) have an OH/H2O (‘3 μm’) band emission maximum of 3690 cm−1 (2.71 μm) indicative of Mg-bearing serpentine, and mildly aqueously altered CMs (≥ 2.5) have a wider band with a complex shape that results from contributions of Fe-bearing serpentine and tochilinite. Among weakly heated CMs (Stage II; 300–500 °C), the low-wavenumber region exhibits spectral features resulting from the dehydration and dehydroxylation of phyllosilicates that include broadening of the Si-O stretching band and a shift of its minimum to lower wavenumber, and the disappearance of the Mg-OH band. The location of the Si-O bending band minimum appears to be unaffected by mild heating. Extensively heated CMs (Stage III+; > 500 °C) have a low-wavenumber region dominated by the spectral features of secondary, Fe-bearing olivine and low-Ca pyroxene and thus are readily distinguished from unheated and mildly heated CMs. The OH/H2O band of all heated CMs is broad and rounded with an emission peak at lower wavenumbers (≤3636 cm−1; ≥2.75 μm) than in unheated CMs. However, spectral and petrographic evidence suggests that our heated CMs have been compromised by terrestrial rehydration. Our study confirms that thermal metamorphism effects are concentrated within the matrix and suggests that the matrix of the CM WIS 91600 had a CI-like mineralogy prior to heating.

The diversity of CM carbonaceous chondrite parent bodies explored using Lewis Cliff 85311

Lewis Cliff (LEW) 85311 is classified as a Mighei-like (CM) carbonaceous chondrite, yet it has some unusual properties that highlight an unrealised diversity within the CMs, and also questions how many parent bodies are sampled by the group. This meteorite is composed of rimmed chondrules, chondrule fragments and refractory inclusions that are set in a fine-grained phyllosilicate-rich matrix. The chondrules are of a similar size to those in the CMs, and have narrow fine-grained rims. LEW 85311 has been mildly aqueously altered, as evidenced by the preservation of melilite and kamacite, and X-ray diffraction results showing a low phyllosilicate fraction and a high ratio of cronstedtite to Fe, Mg serpentine. The chemical composition of LEW 85311 matrix, fine-grained rims, tochilinite and P-rich sulphides is similar to mildly aqueously altered CMs. LEW 85311 is enriched in refractory elements and REEs such that its CI-normalised profile falls between the CMs and CVs, and its oxygen isotopic composition plots in the CV-CK-CO field. Other distinctive properties of this meteorite include the presence of abundant refractory inclusions, and hundreds of micrometer size objects composed of needle-fibre calcite. LEW 85311 could come from part of a single CM parent body that was unusually rich in refractory inclusions, but more likely samples a different parent body to most other members of the group that accreted a subtly different mixture of materials. The mineralogical and geochemical evolution of LEW 85311 during subsequent aqueous alteration was similar to other CMs and was arrested at an early stage, corresponding to a petrologic subtype of CM2.7, probably due to an unusually low proportion of accreted ice. The CM carbonaceous chondrites sample multiple parent bodies whose similar size and inventory of accreted materials, including radiogenic isotopes, led to a comparable post-accretionary evolution.

The alteration history of the Jbilet Winselwan CM carbonaceous chondrite: An analog for C‐type asteroid sample return

AbstractJbilet Winselwan is one of the largest CM carbonaceous chondrites available for study. Its light, major, and trace elemental compositions are within the range of other CM chondrites. Chondrules are surrounded by dusty rims and set within a matrix of phyllosilicates, oxides, and sulfides. Calcium‐ and aluminum‐rich inclusions (CAIs) are present at ≤1 vol% and at least one contains melilite. Jbilet Winselwan is a breccia containing diverse lithologies that experienced varying degrees of aqueous alteration. In most lithologies, the chondrules and CAIs are partially altered and the metal abundance is low (&lt;1 vol%), consistent with petrologic subtypes 2.7–2.4 on the Rubin et al. () scale. However, chondrules and CAIs in some lithologies are completely altered suggesting more extensive hydration to petrologic subtypes ≤2.3. Following hydration, some lithologies suffered thermal metamorphism at 400–500 °C. Bulk X‐ray diffraction shows that Jbilet Winselwan consists of a highly disordered and/or very fine‐grained phase (73 vol%), which we infer was originally phyllosilicates prior to dehydration during a thermal metamorphic event(s). Some aliquots of Jbilet Winselwan also show significant depletions in volatile elements such as He and Cd. The heating was probably short‐lived and caused by impacts. Jbilet Winselwan samples a mixture of hydrated and dehydrated materials from a primitive water‐rich asteroid. It may therefore be a good analog for the types of materials that will be encountered by the Hayabusa‐2 and OSIRIS‐REx asteroid sample‐return missions.

Intense aqueous alteration on C-type asteroids: Perspectives from giant fine-grained micrometeorites

This study explores the petrology of five giant (>400 μm) hydrated fine-grained micrometeorites from the Transantarctic Mountain (TAM) micrometeorite collection. For the first time, the extent and mechanisms of aqueous alteration in unmelted cosmic dust are evaluated and quantified. We use a range of criteria, previously defined for use on hydrated chondrites, including phyllosilicate fraction, matrix geochemistry and micro textures. Collectively, these micrometeorites represent ∼2.22 mm2 of intensely altered hydrated chondritic matrix (with petrologic subtypes of <1.2 in the scheme of Howard et al. (2015)) and reveal a range of alteration styles. Two particles are found to contain pseudomorphic chondrules with thick fine-grained rims, while another micrometeorite contains several aqueously altered CAIs. Their outlines range from well-defined to indistinct, demonstrating that the advanced stages of aqueous alteration progressively remove evidence of coarse-grained components. The remaining two micrometeorites entirely lack coarse-grained components but are similarly altered. Thus, the combined chondrule-to-matrix ratio among these giant micrometeorites is extremely low (6.45 area%), and significantly below the average ratio found in typical CM or CR chondrites (∼20%, Weisberg et al., 2006). Our findings are consistent with previous analyses from smaller Antarctic micrometeorites, which suggest that chondrules (and CAIs) derived from hydrated carbonaceous chondrite parent bodies are underrepresented among the micrometeorite flux, even when considering contributions from coarse-grained micrometeorites. Therefore, to explain the relative paucity of anhydrous material, we propose that the flux of fine-grained micrometeorites is primarily derived from intensely aqueously altered, primitive C-type asteroids, which have lost the majority of their refractory coarse-grained components by replacement with secondary phyllosilicate minerals.

Characterization of matrix material in Northwest Africa 5343: Weathering and thermal metamorphism of the least equilibrated CK chondrite

AbstractBased on the chemical heterogeneity of chondrule and matrix olivine, Northwest Africa (NWA) 5343 is the least metamorphosed CK chondrite reported so far. To better constrain the lower limit of metamorphism in the CK chondrites, we performed a detailed analysis of matrix material in NWA 5343, including characterization of the texture and bulk composition and analyses of individual silicate minerals. Results suggest that NWA 5343 is petrologic type 3.6 or 3.7. Although silicate minerals in the matrix seem to be equilibrated to roughly the same extent throughout the sample, there are recognizable differences in grain size and shape. These textural differences may be the result of transient heating events during impacts, which would be likely on the CK chondrite parent body. The difference between the extent of chemical equilibration and texture may also suggest that grain size and shape are still sensitive to metamorphism at petrologic subtypes where silicate mineral equilibration is nearly complete (e.g., &gt;3.7). Carbonate material present in NWA 5343 is a product of terrestrial weathering; however, infiltration of a Ca‐bearing fluid did not influence the composition of silicate minerals in the matrix. To evaluate the possibility of a continuous metamorphic sequence between the CV and CK chondrites, the bulk matrix composition of NWA 5343 is compared to the CVred chondrite, Vigarano. Although the matrix composition of NWA 5343 could be derived by secondary processing of a Vigarano‐like precursor, porosity and texture of matrix olivine in NWA 5343 are hard to reconcile with a continuous metamorphic sequence.