Northwest Africa 8418: The first CV4 chondrite

Northwest Africa (NWA) 8418 is an unusual chondrite whose properties do not exactly match those of any other known chondrite. It has similarities to the CV (Vigarano group), CK (Karoonda group), and CL (Loongana group) chondrites, but its abundance of large calcium-aluminum-rich inclusions (CAIs) and the low NiO content (<0.2 wt%) of its matrix olivine ally it most closely with the CV group. The absence of grossular, monticellite, wollastonite, and sodalite from the alteration products of the CAIs; the magnesium-rich nature of the matrix olivines (Fa₃₈) relative to that of the CV3 chondrites (~Fa₅₀); and the presence of secondary Na-bearing plagioclase and chlorapatite indicate a metamorphic temperature >600 °C. NWA 8418 contains kamacite, taenite, and troilite, and lacks magnetite and pentlandite. We propose that NWA 8418 be reclassified as a reduced CV4 chondrite, which makes it the first CV chondrite of petrologic type 4.     

Magnetite in the unequilibrated CK chondrites: Implications for metamorphism and new insights into the relationship between the CV and CK chondrites

Bulk isotopic and elemental compositions of CV and CK chondrites have led to the suggestion that both originate from the same asteroid. It has been argued that magnetite compositions also support this model; however, magnetite has been studied almost exclusively in the equilibrated (type 4‐6) CKs. Magnetite in seven unequilibrated CKs analyzed here is enriched in MgO, TiO₂, and Al₂O₃ relative to the equilibrated CKs, suggesting that magnetite compositions are affected by metamorphism. Magnetite in CKs is compositionally distinct from CVs, particularly in abundances of Cr₂O₃, NiO, and TiO₂. Although there are minor similarities between CV and equilibrated CK chondrite magnetite, this is contrary to what we would expect if the CVs and CKs represent a single metamorphic sequence. CV magnetite should resemble CK3 magnetite, as both were metamorphosed to type 3 conditions. Oxygen fugacities and temperatures of CV_ox and CK chondrites are also difficult to reconcile using existing CV‐CK parent body models. Mineral chemistries, which eliminate issues of bulk sample heterogeneity, provide a reliable alternative to techniques that involve a small amount of sample material. CV and CK chondrite magnetite has distinct compositional differences that cannot be explained by metamorphism.     

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

Based 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., >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 CV_red 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.     

Oxygen isotope and chemical compositions of magnetite and olivine in the anomalous CK3 Watson 002 and ungrouped Asuka‐881595 carbonaceous chondrites: Effects of parent body metamorphism

We report in situ O isotope and chemical compositions of magnetite and olivine in chondrules of the carbonaceous chondrites Watson‐002 (anomalous CK3) and Asuka (A)‐881595 (ungrouped C3). Magnetite in Watson‐002 occurs as inclusion‐free subhedral grains and rounded inclusion‐bearing porous grains replacing Fe,Ni‐metal. In A‐881595, magnetite is almost entirely inclusion‐free and coexists with Ni‐rich sulfide and less abundant Ni‐poor metal. Oxygen isotope compositions of chondrule olivine in both meteorites plot along carbonaceous chondrite anhydrous mineral (CCAM) line with a slope of approximately 1 and show a range of Δ¹⁷O values (from approximately ?3 to ?6‰). One chondrule from each sample was found to contain O isotopically heterogeneous olivine, probably relict grains. Oxygen isotope compositions of magnetite in A‐881595 plot along a mass‐dependent fractionation line with a slope of 0.5 and show a range of Δ¹⁷O values from ?2.4‰ to ?1.1‰. Oxygen isotope compositions of magnetite in Watson‐002 cluster near the CCAM line and a Δ¹⁷O value of ?4.0‰ to ?2.9‰. These observations indicate that magnetite and chondrule olivine are in O isotope disequilibrium, and, therefore, not cogenetic. We infer that magnetite in CK chondrites formed by the oxidation of pre‐existing metal grains by an aqueous fluid during parent body alteration, in agreement with previous studies. The differences in Δ¹⁷O values of magnetite between Watson‐002 and A‐881595 can be attributed to their different thermal histories: the former experienced a higher degree of thermal metamorphism that led to the O isotope exchange between magnetite and adjacent silicates.     

Oxygen isotope systematics of chondrule olivine,pyroxene, and plagioclase in one of the most pristine CV3Red chondrites (Northwest Africa 8613)

We performed in situ oxygen three‐isotope measurements of chondrule olivine, pyroxenes, and plagioclase from the newly described CV_Red chondrite NWA 8613. Additionally, oxygen isotope ratios of plagioclase in chondrules from the Kaba CV3_OxB chondrite were determined to enable comparisons of isotope ratios and degree of alteration of chondrules in both CV lithologies. NWA 8613 was affected by only mild thermal metamorphism. The majority of oxygen isotope ratios of olivine and pyroxenes plot along a slope‐1 line in the oxygen three‐isotope diagram, except for a type II and a remolten barred olivine chondrule. When isotopic relict olivine is excluded, olivine, and low‐ and high‐Ca pyroxenes are indistinguishable regarding Δ¹⁷O values. Conversely, plagioclase in chondrules from NWA 8613 and Kaba plot along mass‐dependent fractionation lines. Oxygen isotopic disequilibrium between phenocrysts and plagioclase was caused probably by exchange of plagioclase with ¹⁶O‐poor fluids on the CV parent body. Based on an existing oxygen isotope mass balance model, possible dust enrichment and ice enhancement factors were estimated. Type I chondrules from NWA 8613 possibly formed at moderately high dust enrichment factors (50× to 150× CI dust relative to solar abundances); estimates for water ice in the chondrule precursors range from 0.2× to 0.6× the nominal amount of ice in dust of CI composition. Findings agree with results from an earlier study on oxygen isotopes in chondrules of the Kaba CV chondrite, providing further evidence for a relatively dry and only moderately high dust‐enriched disk in the CV chondrule‐forming region.     

NWA 10214—An LL3 chondrite breccia with an assortment of metamorphosed,shocked, and unique chondrite clasts

NWA 10214 is an LL3‐6 breccia containing ~8 vol% clasts including LL5, LL6, and shocked‐darkened LL fragments as well as matrix‐rich Clast 6 (a new kind of chondrite). This clast is a dark‐colored, subrounded, 6.1 × 7.0 mm inclusion, consisting of 60 vol% fine‐grained matrix, 32 vol% coarse silicate grains, and 8 vol% coarse opaque grains. The large chondrules and chondrule fragments are mainly Type IB; one small chondrule is Type IIA. Also present are one 450 × 600 μm spinel‐pyroxene‐olivine CAI and one 85 × 110 μm AOI. Clast 6 possesses a unique set of properties. (1) It resembles carbonaceous chondrites in having relatively abundant matrix, CAIs, and AOIs; the clast's matrix composition is close to that in CV3 Vigarano. (2) It resembles type‐3 OC in its olivine and low‐Ca pyroxene compositional distributions, and in the Fe/Mn ratio of ferroan olivine grains. Its mean chondrule size is within 1σ of that of H chondrites. The O‐isotopic compositions of the chondrules are in the ordinary‐ and R‐chondrite ranges. (3) It resembles type‐3 enstatite chondrites in the minor element concentrations in low‐Ca pyroxene grains and in having a high low‐Ca pyroxene/olivine ratio in chondrules. Clast 6 is a new variety of type‐3 OC, somewhat more reduced than H chondrites or chondritic clasts in the Netschaevo IIE iron; the clast formed in a nebular region where aerodynamic radial drift processes deposited a high abundance of matrix material and CAIs. A chunk of this chondrite was ejected from its parent asteroid and later impacted the LL body at low relative velocity.     

A clast of Bali‐like oxidized CV material in the reduced CV chondrite breccia Vigarano

Abstract— The CV (Vigarano‐type) chondrites are a petrologically diverse group of meteorites that are divided into the reduced and the Bali‐like and Allende‐like oxidized subgroups largely based on secondary mineralogy (Weisberg et al., 1997; Krot et al., 1998b). Some chondrules and calcium‐aluminum‐rich inclusions (CAIs) in the reduced CV chondrite Vigarano show alteration features similar to those in Allende: metal is oxidized to magnetite; low‐Ca pyroxene, forsterite, and magnetite are rimmed and veined by ferrous olivine (Fs_40–50); and plagioclase mesostases and melilite are replaced by nepheline and sodalite (Sylvester et al., 1993; Kimura and Ikeda, 1996, 1997, 1998). Our petrographic observations indicate that Vigarano also contains individual chondrules, chondrule fragments, and lithic clasts of the Bali‐like oxidized CV materials. The largest lithic clast (about 1 times 2 cm in size) is composed of opaque matrix, type‐I chondrules (400–2000 μm in apparent diameter) surrounded by coarse‐grained and fine‐grained rims, and rare CAIs. The matrix‐chondrule ratio is about 1.1. Opaque nodules in chondrules in the clast consist of Cr‐poor and Cr‐rich magnetite, Ni‐ and Co‐rich metal, Ni‐poor and Ni‐rich sulfide; low‐Ni metal nodules occur only inside chondrule phenocrysts. Chromium‐poor magnetite is preferentially replaced by fayalite. Chondrule mesostases are replaced by phyllosilicates; low‐Ca pyroxene and olivine phenocrysts appear to be unaltered. Matrix in the clast consists of very fine‐grained (<1 μm) ferrous olivine, anhedral fayalite grains (Fa_80–100), rounded objects of porous Ca‐Fe‐rich pyroxenes (Fs_10–50Wo₅₀), Ni‐poor sulfide, Ni‐ and Co‐rich metal, and phyllosilicates; magnetite is rare. On the basis of the presence of the Bali‐like lithified chondritic clast—in addition to individual chondrules and CAIs of both Bali‐like and Allende‐like materials—in the reduced CV chondrite Vigarano, we infer that (1) all three types of materials were mixed during regolith gardening on the CV asteroidal body, and (2) the reduced and oxidized CV materials may have originated from a single, heterogeneously altered asteroid.     

Oxygen isotopes in magnetite and fayalite in CV chondrites Kaba and Mokoia

Abstract— We report in situ measurements of O‐isotopic compositions of magnetite and primary and secondary olivine in the highly unequilibrated oxidized CV chondrites Kaba and Mokoia. In both meteorites, the magnetite and the secondary olivine (fayalite, Fa_90–100) have O‐isotopic compositions near the terrestrial fractionation (TF) line; the mean Δ¹⁷O (= δ¹⁷O‐0.52 × δ¹⁸O) value is about ?1%‰. In contrast, the compositions of nearby primary (chondrule), low‐FeO olivines (Fa_1–2) are well below the TF line; Δ¹⁷O values range from ?3 to ?9%‰. Krot et al. (1998) summarized evidence indicating that the secondary phases in these chondrites formed by aqueous alteration in an asteroidal setting. The compositions of magnetite and fayalite in Kaba and Mokoia imply that the O‐isotopic composition of the oxidant was near or somewhat above the TF line. In Mokoia the fayalite and magnetite differ in δ¹⁸O by ～20%‰, whereas these same materials in Kaba have virtually identical compositions. The difference between Mokoia magnetite and fayalite may indicate formation in isotopic equilibrium in a water‐rich environment at low temperatures, ～300 K. In contrast, the similar compositions of these phases in Kaba may indicate formation of the fayalite by replacement of preexisting magnetite in dry environment, with the O coming entirely from the precursor magnetite and silica. The Δ¹⁷O of the oxidant incorporated into the CV parent body (as phyllosilicates or H₂O) appears to have been much (7–8%‰) lower than that in that incorporated into the LL parent body (Choi et al, 1998), which suggests that the O‐isotopic composition of the nebular gas was spatially or temporally variable.     

An amoeboid olivine inclusion (AOI) in CK3 NWA 1559, comparison to AOIs in CV3 Allende,and the origin of AOIs in CK and CV chondrites

An amoeboid olivine inclusion in CK3 NWA 1559 (0.54 × 1.3 mm) consists of a diopside‐rich interior (approximately 35 vol%) and an olivine‐rich rim (approximately 65 vol%). It is the first AOI to be described in CK chondrites; the apparent paucity of these inclusions is due to extensive parent‐body recrystallization. The AOI interior contains irregular 3–15 μm‐sized Al‐bearing diopside grains (approximately 70 vol%), 2–20 μm‐sized pores (approximately 30 vol%), and traces of approximately 2 μm plagioclase grains. The 75–160 μm‐thick rim contains 20–130 μm‐sized ferroan olivine grains, some with 120º triple junctions. A few coarse (25–50 μm‐sized) patches of plagioclase with 2–18 μm‐thick diopside rinds occur in several places just beneath the rim. The occurrence of olivine rims around AOI‐1 and around many AOIs in CV3 Allende suggests that CK and CV AOIs formed by the acquisition of porous forsteritic rims around fine‐grained, rimless CAIs that consisted of diopside, anorthite, melilite, and spinel. Individual AOIs in carbonaceous chondrites may have formed after transient heating events melted their olivine rims as well as portions of the underlying interiors. In AOI‐1, coarse plagioclase grains with diopside rinds crystallized immediately below the olivine rim. Secondary parent‐body alteration transformed forsterite in the rims of CV and CK AOIs into more‐ferroan olivine. Some of the abundant pores in the interior of AOI‐1 may have formed during aqueous alteration after fine‐grained melilite and anorthite were leached out. Chondrite groups with large chondrules tend to have large AOIs. AOIs that formed in dust‐rich nebular regions (where CV and CK chondrites later accreted) tend to be larger than AOIs from less‐dusty regions.     

Mineralogy,petrography, bulk chemical,iodine-xenon,and oxygen-isotopic compositions of dark inclusions in the reduced CV3 chondrite Efremovka

Abstract— We studied the petrography, mineralogy, bulk chemical, I-Xe, and O-isotopic compositions of three dark inclusions (E39, E53, and E80) in the reduced CV3 chondrite Efremovka. They consist of chondrules, calcium-aluminum-rich inclusions (CAIs), and fine-grained matrix. Primary minerals in chondrules and CAIs are pseudomorphed to various degrees by a mixture largely composed of abundant (>95%), fine-grained (>0.2 μm) fayalitic olivine (Fa_35–42) and minor amounts of chlorite, poorly-crystalline Si-Al-rich material, and chromite; chondrule and CAI shapes and textures are well-preserved. Secondary Ca-rich minerals (Ti-andradite, kirschsteinite, Fe-diopside) are common in chondrule pseudomorphs and matrices in E39 and E80. The degree of replacement increases from E53 to E39 to E80. Fayalitic olivines are heavily strained and contain abundant voids similar to those in incompletely dehydrated phyllosilicates in metamorphosed CM and CI chondrites. Opaque nodules in chondrules consist of Ni- and Co-rich taenite, Co-rich kamacite, and wairauite; sulfides are rare; magnetite is absent. Bulk O-isotopic compositions of E39 and E53 plot in the field of aqueously altered CM chondrites, close to the terrestrial fractionation line; the more heavily altered E39 is isotopically heavier than the less altered E53. The apparent I-Xe age of E53 is 5.4 Ma earlier than Bjurböle and 5.7 ± 2.0 Ma earlier than E39. The I-Xe data are consistent with the most heavily altered dark inclusion, E39 having experienced either longer or later alteration than E53. Bulk lithophile elements in E39 and E53 most closely match those of CO chondrites, except that Ca is depleted and K and As are enriched. Both inclusions are depleted in Se by factors of 3–5 compared to mean CO, CV, CR, or CK chondrites. Zinc in E39 is lower than the mean of any carbonaceous chondrite groups, but in E53 Zn is similar to the means in CO, CV, and CK chondrites. The Efremovka dark inclusions experienced various degrees of aqueous alteration, followed by low degree thermal metamorphism in an asteroidal environment. These processes resulted in preferential oxidation of Fe from opaque nodules and formation of Ni- and Co-rich metal, metasomatic alteration of primary minerals in chondrules and CAIs, and the formation of fayalitic olivine and secondary Ca-Fe-rich minerals. Based on the observed similarities of the alteration mineralization in the Efremovka and Allende dark inclusions, we infer that the latter may have experienced similar alteration processes.     

Origin of the metamorphosed clasts in the CV3 carbonaceous chondrite breccias of Graves Nunataks 06101, Vigarano,Roberts Massif 04143, and Yamato‐86009

We observed metamorphosed clasts in the CV3 chondrite breccias Graves Nunataks 06101, Vigarano, Roberts Massif 04143, and Yamato‐86009. These clasts are coarse‐grained polymineralic rocks composed of Ca‐bearing ferroan olivine (Fa_24–40, up to 0.6 wt% CaO), diopside (Fs_7–12Wo_44–50), plagioclase (An_52–75), Cr‐spinel (Cr/[Cr + Al] = 0.4, Fe/[Fe + Mg] = 0.7), sulfide and rare grains of Fe‐Ni metal, phosphate, and Ca‐poor pyroxene (Fs₂₄Wo₄). Most clasts have triple junctions between silicate grains. The rare earth element (REE) abundances are high in diopside (REE ~3.80–13.83 × CI) and plagioclase (Eu ~12.31–14.67 × CI) but are low in olivine (REE ~0.01–1.44 × CI) and spinel (REE ~0.25–0.49 × CI). These REE abundances are different from those of metamorphosed chondrites, primitive achondrites, and achondrites, suggesting that the clasts are not fragments of these meteorites. Similar mineralogical characteristics of the clasts with those in the Mokoia and Yamato‐86009 breccias (Jogo et al. 2012 ) suggest that the clasts observed in this study would also form inside the CV3 chondrite parent body. Thermal modeling suggests that in order to reach the metamorphosed temperatures of the clasts of >800 °C, the clast parent body should have accreted by ~2.5–2.6 Ma after CAIs formation. The consistency of the accretion age of the clast parent body and the CV3 chondrule formation age suggests that the clasts and CV3 chondrites could be originated from the same parent body with a peak temperature of 800–1100 °C. If the body has a peak temperature of >1100 °C, the accretion age of the body becomes older than the CV3 chondrule formation age and multiple CV3 parent bodies are likely.     

Silicate darkening in the Kobe CK chondrite: Evidence for shock metamorphism at high temperature

Abstract— The Kobe CK4 chondrite, like most metamorphosed CK chondrites, exhibits pronounced silicate darkening of matrix and chondrule mesostases. Our petrographic and scanning electron microscopic study reveals that the matrix of Kobe consists mostly of intermixtures of two types of fine‐grained olivine. One forms subhedral to anhedral normal crystals. The other fills interstices of the subhedral to anhedral olivine crystals, exhibiting a complex network of veinlets. The latter type of olivine contains high densities of small spherical vesicles (<0.05‐3 μm in diameter) and grains (<0.05‐5 μm) of magnetite and pentlandite as well as round to anhedral grains (1–10 μm) of plagioclase, low‐Ca pyroxene, diopside and chlorapatite. The vesicular olivine is particularly abundant in regions of matrix that exhibit a relatively high degree of darkening and commonly fills chondrule mesostases. The vesicular olivine is clearly the principal cause of the silicate darkening in Kobe. The internal texture of the vesicular olivine closely resembles those of local melts produced from the matrices of experimentally and naturally shocked carbonaceous chondrites. The occurrence and texture of the vesicular olivine suggest that it resulted from recrystallization of partially melted matrix olivine by shock. Kobe exhibits light shock effects in olivine that are consistent with shock stage S2 that is too low to explain the occurrence of olivine melting. We suggest that the vesicular olivine in Kobe was produced by shock metamorphism at a relatively mild shock pressure (<25 GPa) and a high temperature (>600 °C). Thus, it is probable that the shock effects in olivine, manifest as fracturing and deformation, were relatively minor, but heating was strong enough to cause partial melting of matrix olivine.     

Chondrules in CK carbonaceous chondrites and thermal history of the CV–CK parent body

CK chondrites are the only group of carbonaceous chondrites with petrologic types ranging from 3 to 6. It is commonly reported than ~15 vol% of CK4–6 samples are composed of chondrules. The modal abundance of chondrules estimated here for 18 CK3–6 (including five CK3s) ranges from zero (totally recrystallized) to 50.5%. Although almost all chemically re‐equilibrated with the host matrix, we recognized in CK3s and Tanezrouft (Tnz) 057 (CK4) up to 85% of chondrules as former type I chondrules. Mean diameters of chondrules range from 0.22 to 1.05 mm for Karoonda (CK4) and Tnz 057 (CK4), respectively. Up to ~60% of chondrules in CK3–4 are surrounded by igneous rims (from ~20 μm to 2 mm width). Zoned olivines were found in unequilibrated chondrules from DaG 431 (CK3‐an), NWA 4724 (CK3.8), NWA 4423 (CK3.9), and Tnz 057 (CK4). We modeled Fe/Mg interdiffusion profiles measured in zoned olivines to evaluate the peak metamorphic temperatures and time scales of the CK parent body metamorphism, and proposed a two‐stage diffusion process in order to account for the position of inflection points situated within chondrules. Time scales inferred from Fe/Mg interdiffusion in olivine from unequilibrated chondrules are on the order of tens to a hundred thousand years (from 50 to 70,000 years for peak metamorphic temperatures of 1140 and 920 K, respectively). These durations are longer than what is commonly accepted for shock metamorphism and shorter than what is required for nuclide decay. Using the concept of a continuous CV–CK metamorphic series, which is reinforced by this study, we estimated peak metamorphic temperatures <850 K for CV, 850–920 K for CK3, and 920–1140 K for CK4–6 chondrites considering a duration of 70,000 years.     

Fayalitic olivine in CV3 chondrite matrix and dark inclusions: A nebular origin

Abstract— Fayalitic olivine (Fa₃₂) is the major component of the matrices and dark inclusions of CV3 and other unequilibrated chondrites. It occurs most commonly as rims, veins and halos in and around chondrule silicates in the Allende-type (CV3_OXA) chondrites and, to a much lesser extent, in the reduced (CV3R) and Bali-type (CV3OXB) chondrites. The olivines have distinctive platy, tabular and lath- or irregular-shaped crystals, with the ratio of the two types varying widely. In CV3_OXB chondrites, matrix fayalitic olivines range up to Fag_99.9; whereas, in the other CV3 chondrites, the range is much smaller. The platy and tabular anisotropic forms of the fayalitic olivines strongly suggest growth from a vapor, and the nature of the occurrences suggests that CV3 matrices are unequilibrated mixtures of nebular materials. We argue that the parent body hydration/dehydration model has numerous inconsistencies that make this hypothesis highly unlikely. These include: (1) There is no direct evidence linking fayalitic olivine to precursor phyllosilicates. (2) Dehydration of phyllosilicates cannot explain the wide range of morphologies of the fayalitic olivines. (3) Fayalitic olivine clearly predates the formation of the hydrous phases in CV3 chondrites and is one of the phases that breaks down to form phyllosilicates (Keller et al., 1994). (4) The unequilibrated nature of the matrix, including fine-scale zoning in 10 μm sized fayalitic olivine crystals, would not survive the parent body metamorphism required in the dehydration model. (5) A dark inclusion in the Ningqiang chondrite contains fayalitic olivine rimmed by glassy and microcrystalline material (Zolensky et al., 1997), which probably formed by radiation damage. This indicates that the fayalitic olivine was exposed to solar radiation in a nebular setting. (6) Some Allende chondrules contain unaltered primary, anhydrous glassy mesostasis in contact with the host matrix (e.g., Ikeda and Kimura, 1995). Chondrule mesostases would not have survived parent body hydration without becoming hydrated and would probably not survive the metamorphic heating required in the dehydration scenario. (7) Single platy and barrel-shaped crystals of fayalitic olivine are present in accretionary rims in calcium-aluminum-rich inclusions (CAIs) (MacPherson and Davis, 1997), which developed in the nebula. (8) Matrix lumps completely encased in chondrules in ordinary chondrites contain mainly fayalitic olivine (Scott et al., 1984), which indicates a nebular origin. (9) Oxygen isotopic compositions of Allende matrix and dark inclusions strongly indicate little or no hydration for Allende and its components (Clayton, 1997). We favor a nebular vaporization/recondensation model in which vaporization of chondritic dust produced a fayalite-rich vapor, followed by formation of the fayalitic olivine by direct recondensation from the vapor, epitactic growth on surfaces of existing forsterite and enstatite in chondrules, and replacement of existing forsterite and enstatite by gas-solid exchange.     

Pecora Escarpment 91002: A member of the new Rumuruti (R) chondrite group

Abstract— Pecora Escarpment (PCA)91002 is a light/dark-structured chondrite breccia related to Carlisle Lakes and Rumuruti; the meteorite contains ～10–20 vol% equilibrated (type ?5 and ?6) clasts within a clastic groundmass, much of which was metamorphosed to type-3.8 levels. The olivine compositional distribution forms a tight cluster that peaks at Fa_38–40; by contrast, low-Ca pyroxene compositions are highly variable. Opaque phases identified in PCA91002 and its paired specimen, PCA91241, include pyrrhotite, pentlandite, pyrite, chromite, ilmenite, metallic Cu and magnetite. The majority of the rock is of shock stage S3-S4; there are numerous sulfide-rich shock veins and 50-μm plagioclase melt pockets. Instrumental neutron activation analysis shows that, unlike Carlisle Lakes and ALH85151, PCA91002 exhibits no Ca enrichment or Au depletion; because PCA91002 is relatively unweathered, it seems probable that the Ca and Au fractionations in Carlisle Lakes and ALH85151 were caused by terrestrial alteration. The Rumuruti-like (formerly Carlisle-Lakes-like) chondrites now include eight separate meteorites. Their geochemical and petrographic similarities suggest that they constitute a distinct chondrite group characterized by unfractionated refractory lithophile abundances (0.95 ± 0.05x CI), high bulk Δ¹⁷O, a low chondrule/groundmass modal abundance ratio, mean chondrule diameters in the 400 ± 100 μm range, abundant NiO-bearing ferroan olivine, sodic plagioclase, titanian chromite, abundant pyrrhotite and pentlandite and negligible metallic Fe-Ni. We propose that this group be called R chondrites after Rumuruti, the only fall. The abundant NiO-bearing ferroan olivine grains, the occurrence of Cu-bearing sulfide, and the paucity of metallic Fe-Ni indicate that R chondrites are highly oxidized. It is unlikely that appreciable oxidation took place on the parent body because of the essential lack of plausible oxidizing agents (e.g., magnetite or hydrated silicates). Therefore, oxidation of R chondrite material must have occurred in the nebula. A few type-I porphyritic olivine chondrules containing olivine grains with cores of Fa_3–4 composition occur in PCA91002; these chondrules probably formed initially as metallic-Fe-Ni-bearing objects at high nebular temperatures. As temperatures decreased and more metallic Fe was oxidized, these chondrules accreted small amounts of oxidized material and were remelted. The ferroan compositions of the >5-μm olivine grains in the R chondrites reflect equilibration with fine-grained FeO-rich matrix material during parent body metatnorphism.     

Petrographic classification of Middle Ordovician fossil meteorites from Sweden

Abstract— The maximum diameter of chromite (FeCr₂O₄) grains within L chondrites reflects the petrographic type of the sample. On the basis of our measurements of nine recent L chondrites, L3 chromite D_max = 34–50 μm, L4 = 87–150 μm, L5 = 76–158 μm, and L6 = 253–638 μm. This variation reflects the crystallization of the chromite grains during parent body thermal metamorphism. We use this calibration to classify six fossil meteorites from the Middle Ordovician in Sweden as type 3 (or 4) to 6. The high flux of L chondrites at 470 Ma contained a range of petrographic types and may have had a higher proportion of lower petrographic type meteorites than are found in recent L chondrite falls. The fossil meteorites have in places preserved recognizable chondrule textures, including porphyritic olivine, barred olivine, and radiating pyroxene. A large relict clast and fusion crust have also been tentatively identified in one fossil meteorite. Apart from chromite, all of the original meteorite minerals have been replaced by carbonate (and sheet silicate and sulfate) during diagenesis within the limestone host. The preservation of chondrule definition has allowed us to measure the mean diameters of relict chondrules. The range (0.4–0.6 mm) is consistent with measurements made in the same way on recent L chondrites.     

Size-frequency distributions of chondrules in CO3 chondrites

Abstract— The size-frequency distributions of chondrules in 11 CO3 chondrites were determined by petrographic analysis of thin sections. CO chondrites have the smallest chondrules of any major chondrite group. In order of decreasing chondrule size, chondrite groups can be arranged as CV ≥ LL > L > H ≥ CM ≥ EH > CO. Chondrule size varies significantly among different CO chondrites; there is a tendency for chondrules to increase in average size with increasing metamorphic grade of the whole-rock. Different chondrule types in CO chondrites have distinct size-frequency distributions: in order of decreasing chondrule size, BO > PO > PP > POP > RP = C. The large size of BO chondrules is problematic; however, PO chondrules are among the largest because ～20% of them contain very coarse relict olivine grains that constitute 40–90 vol.% of the individual chondrules. PP chondrules may be larger than POP chondrules because some of them contain coarse relict pyroxene grains; a compound object consisting of a POP chondrule attached to a large relict pyroxene grain occurs in Lancé. The mean proportions of chondrule types in CO chondrites are estimated to be 69% POP, 18% PP, 8% PO, 2% BO, 2% RP, 1% C and <0.1% GOP. CO chondrites thus contain a smaller proportion of nonporphyritic chondrules than ordinary or EH chondrites, but a larger proportion than CV chondrites. Relative proportions of chondrule types vary with size interval: PO chondrules decrease fairly regularly in abundance with decreasing chondrule size, and RP chondrules appear to be most abundant in the smallest size intervals.     

Secondary calcium-iron-rich minerals in the Bali-like and Allende-like oxidized CV3 chondrites and Allende dark inclusions

Abstract— We have characterized Ca-Fe-rich silicates (salite-hedenbergite pyroxenes (Fs_10–50Wo_45–50), andradite (Ca₃Fe₂Si₃O₁₂), kirschsteinite (CaFeSiO₄), and wollastonite (Ca₃Si₃O₉)) in the type I chondrules and matrices in the Bali-like and Allende-like oxidized CV3 chondrites and Allende dark inclusions. In type I chondrules in the Bali-like CV3 chondrites, metal is oxidized to magnetite; magnetite-sulfide nodules are replaced by Ca-Fe-rich pyroxenes with minor andradite and pure fayalite. We infer that Ca-Fe-rich pyroxenes, andradite, fayalite, magnetite, and phyllosilicates (which occur in mesostases) formed at relatively low temperatures (<300 °C) in the presence of aqueous solutions. Thermodynamic analysis of phase relations in the Si-Fe-Ca-O-H system and large O isotopic fractionation of the coexisting magnetite and fayalite (～20%) (Krot et al., 1998) are consistent with this interpretation. In type I chondrules in the Allende-like CV3 chondrites and dark inclusions, magnetite-sulfide nodules are replaced by Ca-Fe-rich pyroxenes and ferrous olivine; low-Ca pyroxene and forsterite phenocrysts are rimmed and veined by ferrous olivine. It appear that the Ca-Fe-rich pyroxenes predate formation of ferrous olivine; the latter postdates formation of talc and biopyriboles (Brearley, 1997). The Allende dark inclusions are crosscut by Ca-Fe-pyroxene-andradite veins and surrounded by Ca-rich rims that consist of Ca-Fe-rich pyroxenes, andradite, wollastonite, and kirschsteinite. Calcium-rich veins and rims formed after aggregation and lithification of the dark inclusions. The rimmed dark inclusions show zoned depletion in Ca, which is due to a lower abundance of Ca-Fe-rich pyroxenes close to the rim. Calcium was probably leached from the inclusions and redeposited along their edges. We infer that the Allende-like chondrites and dark inclusions experienced similar aqueous alteration to the Bali-like chondrites and were metamorphosed subsequently, which resulted in loss of aqueous solutions and dehydration of phyllosilicates. We conclude that Ca-Fe-rich silicates in the oxidized CV3 chondrites and Allende dark inclusions are secondary and resulted from aqueous fluid-rock interactions during progressive metamorphism of a heterogeneous mixture of hydrous (ices?) and anhydrous materials; the latter were possibly mineralogically similar to the reduced CV3 chondrites.     

Nickel abundance in stony cosmic spherules: Constraining precursor material and formation mechanisms

Abstract– We report bulk and olivine compositions in 66 stony cosmic spherules (Na₂O < 0.76 wt%), 200–800 μm in size, from the Transantarctic Mountains, Antarctica. In porphyritic cosmic spherules, relict olivines that survived atmospheric entry heating are always Ni‐poor and similar in composition to the olivines in carbonaceous or unequilibrated ordinary chondrites (18 spherules), and equilibrated ordinary chondrites (one spherule). This is consistent with selective survival of high temperature, Mg‐rich olivines during atmospheric entry. Olivines that crystallized from the melts produced during atmospheric entry have NiO contents that increase with increasing NiO in the bulk spherule, and that range from values similar to those observed in chondritic olivines (NiO generally <0.5 wt%) to values characteristic of olivines in meteoritic ablation spheres (NiO > 2 wt%). Thus, NiO content in olivine cannot be used alone to distinguish meteoritic ablation spheres from cosmic spherules, and the volatile element contents have to be considered. We propose that the variation in NiO contents in cosmic spherules and their olivines is the result of variable content of Fe, Ni metal in the precursor. NiO contents in olivines and in cosmic spherules can thus be used to discuss their parent body. Ni‐poor spherules can be derived from C‐rich and/or metal‐poor precursors, either related to CM, CI, CR chondrites or to chondritic fragments dominated by silicates, regardless of the parent body. Ni‐rich spherules (NiO > 0.7 wt%) that represent 55% of the 47 barred‐olivine spherules we studied, were derived from the melting of C‐poor, metal‐rich precursors, compatible with ordinary chondrite or CO, CV, CK carbonaceous chondrite parentages.     

Light noble gases in 11 achondrites: Cosmic ray exposure ages,gas retention ages,and preatmospheric sizes

We report light noble gas (He, Ne, and Ar) concentrations and isotopic ratios in 11 achondrites, Tafassasset (unclassified primitive achondrite), Northwest Africa (NWA) 12934 (angrite), NWA 12573 (brachinite), Jiddat al Harasis (JaH) 809 (ureilite), NWA 11562 (ungrouped achondrite), four lodranites (NWA 11901, NWA 7474, NWA 6685, and NWA 6484), NWA 2871 (acapulcoite), and Sahara 02029 (winonaite), most of which have not been previously studied for noble gases. We discuss their noble gas isotopic composition, determine their cosmogenic nuclide content, and systematically calculate their cosmic ray exposure (CRE) and gas retention ages. In addition, we estimate their preatmospheric radii and preatmospheric masses based on the shielding parameter (²²Ne/²¹Ne)_cos. None of the studied meteorites shows evidence of contribution from solar cosmic rays (SCRs). JaH 809 and NWA 12934 show evidence of ³He diffusive losses of >90% and 40%, respectively. The winonaite Sahara 02029 has lost most of its noble gases, either during or before analysis. The average CRE age of Tafassasset of ~49 Ma is lower than that reported by Patzer et al. (2003), but is consistent with it within the uncertainties; this confirms that Tafassasset and CR chondrites are not source paired, CR chondrites having CRE ages from 1 to 25 Ma (Herzog & Caffee, 2014). The ureilite JaH 809 has a CRE age of ~5.4 Ma, which falls into the typical range of exposure ages for ureilites; the angrite NWA 12934 has a CRE age of ~49 Ma, which is within the main range of exposure ages reported for angrites (0.2–56 Ma). We calculate a CRE age of ~2.4 Ma for the brachinite NWA 12573, which falls into a possible “cluster” in the brachinite CRE age histogram around ~3 Ma. Three lodranites (NWA 11901, NWA 7474, and NWA 6685) have CRE ages higher than the average CRE ages of lodranites measured so far, NWA 11901 and NWA 6685 having CRE ages far higher than the CRE age already reported by Li et al. (2019) on NWA 8118. The measured ⁴⁰K-⁴⁰Ar gas retention ages fit well into established systematics. The gas retention age of Tafassasset is consistent, within respective uncertainties, with that previously calculated by Patzer et al. (2003). Our study indicates that Tafassasset originates from a meteoroid with a preatmospheric radius of ~20 cm, however discordant with the radius of ~85 cm inferred in a previous study (Patzer et al., 2003).