Analysis of ordinary chondrites using powder X‐ray diffraction: 2. Applications to ordinary chondrite parent‐body processes

Abstract– We evaluate the chemical and physical conditions of metamorphism in ordinary chondrite parent bodies using X‐ray diffraction (XRD)‐measured modal mineral abundances and geochemical analyses of 48 type 4–6 ordinary chondrites. Several observations indicate that oxidation may have occurred during progressive metamorphism of equilibrated chondrites, including systematic changes with petrologic type in XRD‐derived olivine and low‐Ca pyroxene abundances, increasing ratios of MgO/(MgO+FeO) in olivine and pyroxene, mean Ni/Fe and Co/Fe ratios in bulk metal with increasing metamorphic grade, and linear Fe addition trends in molar Fe/Mn and Fe/Mg plots. An aqueous fluid, likely incorporated as hydrous silicates and distributed homogeneously throughout the parent body, was responsible for oxidation. Based on mass balance calculations, a minimum of 0.3–0.4 wt% H₂O reacted with metal to produce oxidized Fe. Prior to oxidation the parent body underwent a period of reduction, as evidenced by the unequilibrated chondrites. Unlike olivine and pyroxene, average plagioclase abundances do not show any systematic changes with increasing petrologic type. Based on this observation and a comparison of modal and normative plagioclase abundances, we suggest that plagioclase completely crystallized from glass by type 4 temperature conditions in the H and L chondrites and by type 5 in the LL chondrites. Because the validity of using the plagioclase thermometer to determine peak temperatures rests on the assumption that plagioclase continued to crystallize through type 6 conditions, we suggest that temperatures calculated using pyroxene goethermometry provide more accurate estimates of the peak temperatures reached in ordinary chondrite parent bodies.     

Oxygen isotope characteristics of chondrules from the Yamato‐82094 ungrouped carbonaceous chondrite: Further evidence for common O‐isotope environments sampled among carbonaceous chondrites

High‐precision secondary ion mass spectrometry (SIMS) was employed to investigate oxygen three isotopes of phenocrysts in 35 chondrules from the Yamato (Y) 82094 ungrouped 3.2 carbonaceous chondrite. Twenty‐one of 21 chondrules have multiple homogeneous pyroxene data (?¹⁷O 3SD analytical uncertainty: 0.7‰); 17 of 17 chondrules have multiple homogeneous pyroxene and plagioclase data. Twenty‐one of 25 chondrules have one or more olivine data matching coexisting pyroxene data. Such homogeneous phenocrysts (1) are interpreted to have crystallized from the final chondrule melt, defining host O‐isotope ratios; and (2) suggest efficient O‐isotope exchange between ambient gas and chondrule melt during formation. Host values plot within 0.7‰ of the primitive chondrule mineral (PCM) line. Seventeen chondrules have relict olivine and/or spinel, with some δ¹⁷O and δ¹⁸O values approaching ?40‰, similar to CAI or AOA‐like precursors. Regarding host chondrule data, 22 of 34 have Mg#s of 98.8–99.5 and ?¹⁷O of ?3.9‰ to ?6.1‰, consistent with most Acfer 094, CO, CR, and CV chondrite chondrules, and suggesting a common reduced O‐isotope reservoir devoid of ¹⁶O‐poor H₂O. Six Y‐82094 chondrules have ?¹⁷O near ?2.5‰, with Mg#s of 64–97, consistent with lower Mg# chondrules from Acfer 094, CO, CR, and CV chondrites; their signatures suggest precursors consisting of those forming Mg# ~99, ?¹⁷O: ?5‰ ± 1‰ chondrules plus ¹⁶O‐poor H₂O, at high dust enrichments. Three type II chondrules plot slightly above the PCM line, near the terrestrial fractionation line (?¹⁷O: ~+0.1‰). Their O‐isotopes and olivine chemistry are like LL3 type II chondrules, suggesting they sampled ordinary chondrite‐like chondrule precursors. Finally, three Mg# >99 chondrules have ?¹⁷O of ?6.7‰ to ?8.1‰, potentially due to ¹⁶O‐rich refractory precursor components. The predominance of Mg# ~99, ?¹⁷O: ?5‰ ± 1‰ chondrules and a high chondrule‐to‐matrix ratio suggests bulk Y‐82094 characteristics are closely related to anhydrous dust sampled by most carbonaceous chondrite chondrules.     

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.     

A critical evaluation of oxidation versus reduction during metamorphism of L and LL group chondrites,and implications for asteroid spectroscopy

Abstract— Modal mineralogies of individual, equilibrated (petrologic type 4–6 L and LL chondrites have been measured using an electron microprobe mapping technique, and the chemical compositions of coexisting silicate minerals have been analyzed. Progressive changes in the relative abundances and in the molar Fe/Mn and Fe/Mg ratios of olivine, low‐Ca pyroxene, and diopside occur with increasing metamorphic grade. Variations in olivine/low‐Ca pyroxene ratios (Ol/Px) and in metal abundances and compositions with petrologic type support the hypothesis that oxidation of metallic iron accompanied thermal metamorphism in ordinary chondrites. Modal Ol/Px ratios are systematically lower than normative Ol/Px ratios for the same meteorites, suggesting that the commonly used C.I.P.W. norm calculation procedure may not adequately estimate silicate mineral abundances in reduced chondrites. Ol/Px ratios calculated from visible and near‐infrared (VISNIR) reflectance spectra of the same meteorites are not in agreement with other Ol/Px determinations, possibly because of spectral complexities arising from other minerals in chondrites. Characteristic features in VISNIR spectra are sensitive to the proportions and compositions of olivine and pyroxenes, the minerals most affected by oxidative metamorphism. This work may allow spectral calibration for the determination of mineralogy and petrologic type, and thus may be useful for spectroscopic studies of asteroids.     

The Fountain Hills impact‐modified CB chondrite and thermal history of the CB asteroid

Abstract— Fountain Hills is a metal‐rich chondrite with mineral and whole chondrite oxygen isotope compositions that suggest it is a CB chondrite. However, its petrologic characteristics suggest that it has been modified by shock and recrystallization to a greater degree than other CB chondrites. It differs texturally from the CB chondrites in that its metal is interstitial to the silicate and does not occur as discrete clasts as in the other CB chondrites. Portions of Fountain Hills appear to be recrystallized and it contains large (mm‐size) olivine rimmed by pyroxene. A characteristic of the CB chondrites is the presence of small sulfide blebs in large metal clasts and anomalously heavy (¹⁵N‐enriched) nitrogen often associated with metal surrounding the sulfide blebs, but Fountain Hills lacks sulfide and its nitrogen is relatively light. The differences between Fountain Hills and the other CB chondrites can be attributed to a secondary process, most likely impact‐melting and recrystallization, that overprinted its primary features and it is inferred that Fountain Hills is an impact‐modified CB chondrite.     

Northwest Africa 428: Impact‐induced annealing of an L6 chondrite breccia

Abstract— Northwest Africa (NWA) 428 is an L chondrite that was successively thermally metamorphosed to petrologic type‐6, shocked to stage S4–S5, brecciated, and annealed to approximately petrologic type‐4. Its thermal and shock history resembles that of the previously studied LL6 chondrite, Miller Range (MIL) 99301, which formed on a different asteroid. The petrologic type‐6 classification of NWA 428 is based on its highly recrystallized texture, coarse metal (150 ± 150 μm), troilite (100 ± 170 μm), and plagioclase (20–60 μm) grains, and relatively homogeneous olivine (Fa_{24.4 ± 0.6}), low‐Ca pyroxene (Fs_{20.5 ± 0.4}), and plagioclase (Ab_{84.2 ± 0.4}) compositions. The petrographic criteria that indicate shock stage S4–S5 include the presence of chromite veinlets, chromite‐plagioclase assemblages, numerous occurrences of metallic Cu, irregular troilite grains within metallic Fe‐Ni, polycrystalline troilite, duplex plessite, metal and troilite veins, large troilite nodules, and low‐Ca clinopyroxene with polysynthetic twins. If the rock had been shocked before thermal metamorphism, low‐Ca clinopyroxene produced by the shock event would have transformed into orthopyroxene. Post‐shock brecciation is indicated by the presence of recrystallized clasts and highly shocked clasts that form sharp boundaries with the host. Post‐shock annealing is indicated by the sharp optical extinction of the olivine grains; during annealing, the damaged olivine crystal lattices healed. If temperatures exceeded those approximating petrologic type‐4 (?600–700°C) during annealing, the low‐Ca clinopyroxene would have transformed into orthopyroxene. The other shock indicators, likewise, survived the mild annealing. An impact event is the most plausible source of post‐metamorphic, post‐shock annealing because any ²⁶Al that may have been present when the asteroid accreted would have decayed away by the time NWA 428 was annealed. The similar inferred histories of NWA 428 (L6) and MIL 99301 (LL6) indicate that impact heating affected more than 1 ordinary chondrite parent body.     

Oxygen isotopes in chondrule olivine and isolated olivine grains from the CO3 chondrite Allan Hills A77307

Abstract— We have measured O‐isotopic ratios in a variety of olivine grains in the CO3 chondrite Allan Hills (ALH) A77307 using secondary ion mass spectrometry in order to study the chondrule formation process and the origin of isolated olivine grains in unequilibrated chondrites. Oxygen‐isotopic ratios of olivines in this chondrite are variable from δ¹⁷O = ?15.5 to +4.5% and δ¹⁸O = ?11.5 to +3.9%, with Δ¹⁷O varying from ?10.4 to +3.5%. Forsteritic olivines, Fa_<1, are enriched in ¹⁶O relative to the bulk chondrite, whereas more FeO‐rich olivines are more depleted in ¹⁶O. Most ratios lie close to the carbonaceous chondrite anhydrous minerals (CCAM) line with negative values of Δ¹⁷O, although one grain of composition Fa₄ has a mean Δ¹⁷O of +1.6%. Marked O‐isotopic heterogeneity within one FeO‐rich chondrule is the result of incorporation of relic, ¹⁶O‐rich, Mg‐rich grains into a more ¹⁶O‐depleted host. Isolated olivine grains, including isolated forsterites, have similar O‐isotopic ratios to olivine in chondrules of corresponding chemical composition. This is consistent with derivation of isolated olivine from chondrules, as well as the possibility that isolated grains are chondrule precursors. The high ¹⁶O in forsteritic olivine is similar to that observed in forsterite in CV and CI chondrites and the ordinary chondrite Julesburg and suggests nebula‐wide processes for the origin of forsterite that appears to be a primitive nebular component.     

Heavily metamorphosed clasts from the CV chondrite breccias Mokoia and Yamato‐86009

Abstract– Metamorphosed clasts in the CV carbonaceous chondrite breccias Mokoia and Yamato‐86009 (Y‐86009) are coarse‐grained, granular, polymineralic rocks composed of Ca‐bearing (up to 0.6 wt% CaO) ferroan olivine (Fa_34–39), ferroan Al‐diopside (Fs_9–13Wo_47–50, approximately 2–7 wt% Al₂O₃), plagioclase (An_37–84Ab_63–17), Cr‐spinel (Cr/(Cr + Al) = 0.19–0.45, Fe/(Fe + Mg) = 0.60–0.79), nepheline, pyrrhotite, pentlandite, Ca‐phosphate, and rare grains of Ni‐rich taenite; low‐Ca pyroxene is absent. Most clasts have triple junctions between silicate grains, indicative of prolonged thermal annealing. Based on the olivine‐spinel and pyroxene thermometry, the estimated metamorphic temperature recorded by the clasts is approximately 1100 K. Few clasts experienced thermal metamorphism to a lower degree and preserved chondrule‐like textures. The Mokoia and Y‐86009 clasts are mineralogically unique and different from metamorphosed chondrites of known groups (H, L, LL, R, EH, EL, CO, CK) and primitive achondrites (acapulcoites, brachinites, lodranites). On a three‐isotope oxygen diagram, compositions of olivine in the clasts plot along carbonaceous chondrite anhydrous mineral line and the Allende mass‐fractionation line, and overlap with those of the CV chondrule olivines; the Δ¹⁷O values of the clasts range from about ?4.3‰ to ?3.0‰. We suggest that the clasts represent fragments of the CV‐like material that experienced metasomatic alteration, high‐temperature metamorphism, and possibly melting in the interior of the CV parent asteroid. The lack of low‐Ca pyroxene in the clasts could be due to its replacement by ferroan olivine during iron‐alkali metasomatic alteration or by high‐Ca ferroan pyroxene during melting under oxidizing conditions.     

Subtype 3.0 chondrites: Petrologic classification criteria

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.     

Compositional diversity of ordinary chondrites inferred from petrology,bulk chemical,and oxygen isotopic compositions of the lowest FeO ordinary chondrite,Yamato 982717

We performed a petrologic, geochemical, and oxygen isotopic study of the lowest FeO ordinary chondrite (OC), Yamato (Y) 982717. Y 982717 shows a chondritic texture composed of chondrules and chondrule fragments, and mineral fragments set in a finer grained, clastic matrix, similar to H4 chondrites. The composition of olivine (Fa_{11.17 ± 0.48 (1σ)}) and low‐Ca pyroxene (Fs_{11.07 ± 0.98 (1σ)}Wo_{0.90 ± 0.71(1σ)}) is significantly more magnesian than those of typical H chondrites (Fa_16.0‐20, Fs_14.5‐18.0), as well as other known low‐FeO OCs (Fa_12.8‐16.7; Fs_13‐16). However, the bulk chemical composition of Y 982717, in particular lithophile and moderately volatile elements, is within the range of OCs. The bulk siderophile element composition (Ni, Co) is within the range of H chondrites and distinguishable from L chondrites. The O‐isotopic composition is also within the range of H chondrites. The lack of reduction textures indicates that the low olivine Fa content and low‐Ca pyroxene Fs content are characteristics of the precursor materials, rather than the result of reduction during thermal metamorphism. We suggest that the H chondrites are more compositionally diverse than has been previously recognized.     

CHEMICAL COMPOSITION,PETROGRAPHY AND MINERALOGY OF THE SHIBAYAMA CHONDRITE FOUND IN SHIBAYAMA-MACHI,SANBU-GUN,CHIBA-KEN,JAPAN

In April 1969, the chondrite was accidentally found in the side wall of the vegetable storage excavated at Shibayama-machi, Sanbu-gun, Chiba-ken, Japan, by Mr. A. Ishii and his grandson, Mr. S. Ito. The chondrite named Shibayama has been weathered thoroughly for a long period of burial underground. The bulk chemical composition, especially total Fe (21.41%) and ratios of Fe_total/SiO₂(0.557), SiO₂/MgO (1.59) and molar composition of olivine (Fa₂₃) and pyroxene (Fs₂₂) as well as mineral composition, indicate that Shibayama is a typical olivine-hypersthene chondrite. If the oxidized Fe is assumed only from metallic Fe, the original metallic Fe (7.75%) and Fe_metal/Fe_total(0.361) also support the above conclusion. From the well-recrystallized texture, indistinct and obliterated chondrule-matrix boundary, homogeneous composition of olivine and pyroxene, absence of igneous glass, and interstitial and well-developed plagioclase, this chondrite could be classified in petrologic type 6. Mosaic texture, kink bands, undulatory extinction of silicate grains and maskelynitization of plagioclase indicate that Shibayama suffered from a heavy shock effect, as is seen in other L-6 group chondrites.     

Geochemical and oxygen isotope perspective of a new R chondrite Dhofar 1671: Affinity with ordinary chondrites

Dhofar 1671 is a relatively new meteorite that previous studies suggest belongs to the Rumuruti chondrite class. Major and REE compositions are generally in agreement with average values of the R chondrites (RCs). Moderately volatile elements such as Se and Zn abundances are lower than the R chondrite values that are similar to those in ordinary chondrites (OCs). Porphyritic olivine pyroxene (POP), radial pyroxene (RP), and barred olivine (BO) chondrules are embedded in a proportionately equal volume of matrix, one of the characteristic features of RCs. Microprobe analyses demonstrate compositional zoning in chondrule and matrix olivines showing Fa‐poor interior and Fa‐rich outer zones. Precise oxygen isotope data for chondrules and matrix obtained by laser‐assisted fluorination show a genetic isotopic relationship between OCs and RCs. On the basis of our data, we propose a strong affinity between these groups and suggest that OC chondrule precursors could have interacted with a ¹⁷O‐rich matrix to form RC chondrules (i.e., ?¹⁷O shifts from ~1‰ to ~3‰). These interactions could have occurred at the same time as “exotic” clasts in brecciated samples formed such as NWA 10214 (LL3–6), Parnallee (LL3), PCA91241 (R3.8–6), and Dhofar 1671 (R3.6). We also infer that the source of the oxidation and ¹⁷O enrichment is the matrix, which may have been enriched in ¹⁷O‐rich water. The abundance of matrix in RCs relative to OCs, ensured that these rocks would be apparently more oxidized and appreciably ¹⁷O‐enriched. In situ analysis of Dhofar 1671 is recommended to further strengthen the link between OCs and RCs.     

Acfer 217-A new member of the Rumuruti chondrite group (R)

Abstract— Previously, three meteorites from Australia and Antarctica were described as a new chondritic “grouplet” (Carlisle Lakes, Allan Hills (ALH) 85151, Yamato (Y) ?75302; Rubin and Kallemeyn, 1989). This grouplet was classified as the “Carlisle Lakes-type” chondrites (Weisberg et al., 1991). Recently, one Saharan sample and four more Antarctic meteorites were identified to belong to this group (Acfer 217, Y-793575, Y-82002, PCA91002, PCA91241). The latter two are probably paired. With the meteorite Rumuruti, the first fall of this type of chondrite is known (Schulze et al., 1994). We report here on the Saharan meteorite Acfer 217 which has chemical and mineralogical properties very similar to Rumuruti and Carlisle Lakes. All eight members of this group, Rumuruti, Carlisle Lakes, ALH85151, Y-75302, Y-793575, Y-82002, Acfer 217, and the paired samples PCA91002 and PCA91241 justify the introduction of a new group of chondritic meteorites, the Rumuruti meteorites (R). Acfer 217 is a regolith breccia consisting of up to cm-sized clasts (～33 vol%) embedded in a fine-grained, well-lithified clastic matrix. The most abundant mineral is olivine (～72 vol%), which has a high Fa-content of 37–39 mol%. The major minerals (olivine, low-Ca pyroxene, Ca-pyroxene, and plagioclase) show some compositional variability indicating a slightly unequilibrated nature of the meteorite. Considering the mean olivine composition of Fa_{37.8 ± 5.7}, a classification of Acfer 217 as a R3.8 chondrite would result; however, Acfer 217 is a regolith breccia consisting of clasts of various petrologic types. Therefore, we suggest to classify Acfer 217 as a R3–5 chondrite regolith breccia. The bulk meteorite is very weakly shocked (S2). The bulk composition of Acfer 217 and other R-meteorites show that the R-meteorites are basically chondritic in composition. The pattern of moderately volatile elements is unique in R chondrites; Na and Mn are essentially undepleted, similar to ordinary chondrites, while Zn and Se contents are similar to concentrations in CM chondrites. The oxygen isotopic composition in Acfer 217 is similar to that of Rumuruti, Carlisle Lakes, ALH 85151, and Y-75302. In a δ¹⁷O vs. δ¹⁸O-diagram, the R-meteorites form a group well resolved from other chondrite groups. Acfer 217 was a meteoroid of common size with a radius between 15–65 cm and with a single stage exposure history. Based on ²¹Ne, an exposure age of about 35 Ma was calculated.     

Mineralogy,petrology, and oxygen isotopic compositions of chondritic and achondritic lithologies in the anomalous CB carbonaceous chondrites Sierra Gorda 013 and Fountain Hills

The CB (Bencubbin-like) metal-rich carbonaceous chondrites are subdivided into the CB_a and CB_b subgroups. The CB_a chondrites are composed predominantly of ~cm-sized skeletal olivine chondrules and unzoned Fe,Ni-metal ± troilite nodules. The CB_b chondrites are finer grained than the CB_as and consist of chemically zoned and unzoned Fe,Ni-metal grains, Fe,Ni-metal ± troilite nodules, cryptocrystalline and skeletal olivine chondrules, and rare refractory inclusions. Both subgroups contain exceptionally rare porphyritic chondrules and no interchondrule fine-grained matrix, and are interpreted as the products of a gas–melt impact plume formed by a high-velocity collision between differentiated planetesimals about 4562 Ma. The anomalous metal-rich carbonaceous chondrites, Fountain Hills and Sierra Gorda 013 (SG 013), have bulk oxygen isotopic compositions similar to those of other CBs but contain coarse-grained igneous clasts/porphyritic chondrule-like objects composed of olivine, low-Ca-pyroxene, and minor plagioclase and high-Ca pyroxene as well as barred olivine and skeletal olivine chondrules. Cryptocrystalline chondrules, zoned Fe,Ni-metal grains, and interchondrule fine-grained matrix are absent. In SG 013, Fe,Ni-metal (~80 vol%) occurs as several mm-sized nodules; magnesiochromite (Mg-chromite) is accessory; daubréelite and schreibersite are minor; troilite is absent. In Fountain Hills, Fe,Ni-metal (~25 vol%) is dispersed between chondrules and silicate clasts; chromite and sulfides are absent. In addition to a dominant chondritic lithology, SG 013 contains a chondrule-free lithology composed of Fe,Ni-metal nodules (~25 vol%), coarse-grained olivine and low-Ca pyroxene, interstitial high-Ca pyroxene and anorthitic plagioclase, and Mg-chromite. Here, we report on oxygen isotopic compositions of olivine, low-Ca pyroxene, and ±Mg-chromite in Fountain Hills and both lithologies of SG 013 measured in situ using an ion microprobe. Oxygen isotope compositions of olivine, low-Ca pyroxene, and Mg-chromite in these meteorites are similar to those of magnesian non-porphyritic chondrules in CB_a and CB_b chondrites: on a three-isotope oxygen diagram (δ¹⁷O vs. δ¹⁸O), they plot close to a slope-1 (primitive chondrule mineral) line and have a very narrow range of Δ¹⁷O (=δ¹⁷O–0.52 × δ¹⁸O) values, −2.5 ± 0.9‰ (avr ± 2SD). No isotopically distinct relict grains have been identified in porphyritic chondrule-like objects. We suggest that magnesian non-porphyritic (barred olivine, skeletal olivine, cryptocrystalline) chondrules in the CB_as, CB_bs, and porphyritic chondrule-like objects in SG 013 and Fountain Hills formed in different zones of the CB impact plume characterized by variable pressure, temperature, cooling rates, and redox conditions. The achondritic lithology in SG 013 represents fragments of one of the colliding bodies and therefore one of the CB chondrule precursors. Fountain Hills was subsequently modified by impact melting; Fe,Ni-metal and sulfides were partially lost during this process.     

Saint-Pierre-le-Viger (L5-6) from asteroid 2023 CX1 recovered in the Normandy,France—220 years after the historic fall of L'Aigle (L6 breccia) in the neighborhood

On February 13, 2023, a huge fireball was visible over Western Europe (fireball event 2023 CX₁). After the possible strewn field was calculated, the first of several recovered samples, with a mass of about 100 g, was discovered just 2 days after the fireball event on the ground of the village of Saint-Pierre-le-Viger. Meanwhile, more than 60 samples with a total mass of more than 1 kg were recovered and a piece of one of these is studied here. The fall occurred 220 years after the historic meteorite fall of L'Aigle on April 26, 1803, <120 km south. L'Aigle is the closest meteorite fall to Saint-Pierre-le-Viger and belongs to the same chondrite group. Both meteorites are breccias containing only clasts of high metamorphic degree (type 5 and type 6). Since only 20% of the L chondrites are breccias this coincidence is remarkable. As just mentioned, both samples studied from these rocks in this work are ordinary chondrite breccias and consist of equilibrated and recrystallized lithologies of petrologic type 6. The brecciated texture in L'Aigle, resulting in a remarkable light–dark structure, is more pronounced than the brecciated features in Saint-Pierre-le-Viger, from which also type 5 fragments have been reported. The compositions of low-Ca pyroxene and olivine grains in Saint-Pierre-le-Viger (Fs_21.2 and Fa_23.4, respectively) clearly require an L-group classification. L'Aigle was classified as an L6 breccia in the past, and this has now been confirmed by new data on low-Ca pyroxene and olivine (Fs_20.7 and Fa_23.8, respectively). Saint-Pierre-le-Viger contains local thin shock veins, and both meteorites are moderately shocked. Most olivines in the studied samples have planar fractures, but the estimated abundance of mosaicized olivines of 30%–40% among the large grains require a S4 shock classification. Oxygen isotope and bulk chemical data of Saint-Pierre-le-Viger certainly support the L chondrite classification. Bulk spectral data of Saint-Pierre-le-Viger are dominated by silicate minerals, that is, Fe-bearing low-Ca pyroxene, olivine, and plagioclase. Isotopic, chemical, and spectral data of the L'Aigle meteorite are shown for comparison and are very similar, providing additional circumstantial evidence of Saint-Pierre-le-Viger's L chondritic nature.     

Analysis of ordinary chondrites using powder X‐ray diffraction: 1. Modal mineral abundances

Abstract– Powder X‐ray diffraction (XRD) is used to quantify the modal abundances (in wt%) of 18 H, 17 L, and 13 LL unbrecciated ordinary chondrite falls, which represents the complete petrologic range of equilibrated ordinary chondrites (types 4–6). The XRD technique presents an effective alternative to traditional methods for determining modal abundances, such as optical point counting and electron microprobe phase (EMP) mapping. The majority of chondrite powders in this study were previously prepared for chemical characterization from 8 to 20 g of material, which is consistent with the suggested mass (10 g) necessary to provide representative sampling of ordinary chondrites. Olivine and low‐Ca pyroxene are the most abundant phases present, comprising one‐half to three‐fourths of total abundances, while plagioclase, high‐Ca pyroxene, troilite, and metal comprise the remaining XRD‐measured mineralogy. Pigeonite may also be present in some samples, but it is fitted using a high‐Ca pyroxene standard, so exact abundances cannot be measured directly using XRD. Comparison of XRD‐measured abundances with calculated Cross, Iddings, Pirsson, Washington (CIPW) normative abundances indicates that systematic discrepancies exist between these two data sets, particularly in olivine and high‐Ca pyroxene. This discrepancy is attributed to the absence of pigeonite as a possible phase in the CIPW normative mineralogy. Oxides associated with pigeonite are improperly allocated, resulting in overestimated normative olivine abundances and underestimated normative high‐Ca pyroxene abundances. This suggests that the CIPW norm is poorly suited for determining mineralogical modal abundances of ordinary chondrites.     

Petrology and oxygen isotopic compositions of calcium‐aluminum‐rich inclusions in primitive CO3.0‐3.1 chondrites

The petrologic and oxygen isotopic characteristics of calcium‐aluminum‐rich inclusions (CAIs) in CO chondrites were further constrained by studying CAIs from six primitive CO3.0‐3.1 chondrites, including two Antarctic meteorites (DOM 08006 and MIL 090010), three hot desert meteorites (NWA 10493, NWA 10498, and NWA 7892), and the Colony meteorite. The CAIs can be divided into hibonite‐bearing inclusions (spinel‐hibonite spherules, monomineralic grains, hibonite‐pyroxene microspherules, and irregular/nodular objects), grossite‐bearing inclusions (monomineralic grains, grossite‐melilite microspherules, and irregular/nodular objects), melilite‐rich inclusions (fluffy Type A, compact type A, monomineralic grains, and igneous fragments), spinel‐pyroxene inclusions (fluffy objects resembling fine‐grained spinel‐rich inclusions in CV chondrites and nodular/banded objects resembling those in CM chondrites), and pyroxene‐anorthite inclusions. They are typically small (98.4 ± 54.4 µm, 1SD) and comprise 1.54 ± 0.43 (1SD) area% of the host chondrites. Melilite in the hot desert and Colony meteorites was extensively replaced by a hydrated Ca‐Al‐silicate during terrestrial weathering and converted melilite‐rich inclusions into spinel‐pyroxene inclusions. The CAI populations of the weathered COs are very similar to those in CM chondrites, suggesting that complete replacement of melilite by terrestrial weathering, and possibly parent body aqueous alteration, would make the CO CAIs CM‐like, supporting the hypothesis that CO and CM chondrites derive from similar nebular materials. Within the CO3.0‐3.1 chondrites, asteroidal alteration significantly resets oxygen isotopic compositions of CAIs in CO3.1 chondrites (?¹⁷O: ?25 to ?2‰) but left those in CO3.0‐3.05 chondrites mostly unchanged (?¹⁷O: ?25 to ?20‰), further supporting the model whereby thermal metamorphism became evident in CO chondrites of petrologic type ≥3.1. The resistance of CAI minerals to oxygen isotope exchange during thermal metamorphism follows in the order: melilite + grossite < hibonite + anorthite < spinel + diopside + forsterite. Meanwhile, terrestrial weathering destroys melilite without changing the chemical and isotopic compositions of melilite and other CAI minerals.     

Phosphate and feldspar mineralogy of equilibrated L chondrites: The record of metasomatism during metamorphism in ordinary chondrite parent bodies

In ordinary chondrites (OCs), phosphates and feldspar are secondary minerals known to be the products of parent‐body metamorphism. Both minerals provide evidence that metasomatic fluids played a role during metamorphism. We studied the petrology and chemistry of phosphates and feldspar in petrologic type 4–6 L chondrites, to examine the role of metasomatic fluids, and to compare metamorphic conditions across all three OC groups. Apatite in L chondrites is Cl‐rich, similar to H chondrites, whereas apatite in LL chondrites has lower Cl/F ratios. Merrillite has similar compositions among the three chondrite groups. Feldspar in L chondrites shows a similar equilibration trend to LL chondrites, from a wide range of plagioclase compositions in petrologic type 4 to a homogeneous albitic composition in type 6. This contrasts with H chondrites which have homogeneous albitic plagioclase in petrologic types 4–6. Alkali‐ and halogen‐rich and likely hydrous metasomatic fluids acted during prograde metamorphism on OC parent bodies, resulting in albitization reactions and development of phosphate minerals. Fluid compositions transitioned to a more anhydrous, Cl‐rich composition after the asteroid began to cool. Differences in secondary minerals between H and L, LL chondrites can be explained by differences in fluid abundance, duration, or timing of fluid release. Phosphate minerals in the regolith breccia, Kendleton, show lithology‐dependent apatite compositions. Bulk Cl/F ratios for OCs inferred from apatite compositions are higher than measured bulk chondrite values, suggesting that bulk F abundances are overestimated and that bulk Cl/F ratios in OCs are similar to CI.     

Calcium‐aluminum‐rich inclusions and amoeboid olivine aggregates from the CR carbonaceous chondrites

Abstract— Calcium‐aluminum‐rich refractory inclusions (CAIs) in CR chondrites are rare (<1 vol%), fairly small (<500 μm) and irregularly‐shaped, and most of them are fragmented. Based on the mineralogy and petrography, they can be divided into grossite ± hibonite‐rich, melilite‐rich, and pyroxene‐anorthite‐rich CAIs. Other types of refractory objects include fine‐grained spinel‐melilite‐pyroxene aggregates and amoeboid olivine aggregates (AOAs). Some of the pyroxene‐anorthite‐rich CAIs have igneous textures, and most melilite‐rich CAIs share similarities to both the fluffy and compact type A CAIs found in CV chondrites. One major difference between these CAIs and those in CV, CM, and CO chondrites is that secondary mineral phases are rare. In situ ion microprobe analyses of oxygen‐isotopic compositions of 27 CAIs and AOAs from seven CR chondrites demonstrate that most of the CAIs are ¹⁶O‐rich (δ¹⁷O of hibonite, melilite, spinel, pyroxene, and anorthite < ?22‰) and isotopically homogeneous within 3–4‰. Likewise, forsterite, spinel, anorthite, and pyroxene in AOAs have nearly identical, ¹⁶O‐rich compositions (?24‰ < δ¹⁷O < ?20‰). In contrast, objects which show petrographic evidence for extensive melting are not as ¹⁶O‐rich (δ¹⁷O less than ?18‰). Secondary alteration minerals replacing ¹⁶O‐rich melilite in melilite‐rich CAIs plot along the terrestrial fractionation line. Most CR CAIs and AOAs are mineralogically pristine objects that largely escaped thermal metamorphism and secondary alteration processes, which is reflected in their relatively homogeneous ¹⁶O‐rich compositions. It is likely that these objects (or their precursors) condensed in an ¹⁶O‐rich gaseous reservoir in the solar nebula. In contrast, several igneous CAIs are not very enriched in ¹⁶O, probably as a result of their having melted in the presence of a relatively ¹⁶O‐poor nebular gas. If the precursors of these CAIs were as ¹⁶O‐rich as other CR CAIs, this implies either temporal excursions in the isotopic composition of the gas in the CAI‐forming regions and/or radial transport of some CAI precursors into an ¹⁶O‐poor gas. The absence of oxygen isotope heterogeneity in the primary minerals of melilite‐rich CAIs containing alteration products suggests that mineralogical alteration in CR chondrites did not affect oxygen‐isotopic compositions of their CAIs.     

Refractory calcium‐aluminum‐rich inclusions and aluminum‐diopside‐rich chondrules in the metal‐rich chondrites Hammadah al Hamra 237 and Queen Alexandra Range 94411

Abstract— The metal‐rich chondrites Hammadah al Hamra (HH) 237 and Queen Alexandra Range (QUE) 94411, paired with QUE 94627, contain relatively rare (<1 vol%) calcium‐aluminum‐rich inclusions (CAIs) and Al‐diopside‐rich chondrules. Forty CAIs and CAI fragments and seven Al‐diopside‐rich chondrules were identified in HH 237 and QUE 94411/94627. The CAIs, ～50–400 μm in apparent diameter, include (a) 22 (56%) pyroxene‐spinel ± melilite (+forsterite rim), (b) 11 (28%) forsterite‐bearing, pyroxene‐spinel ± melilite ± anorthite (+forsterite rim) (c) 2 (5%) grossite‐rich (+spinel‐melilite‐pyroxene rim), (d) 2 (5%) hibonite‐melilite (+spinel‐pyroxene ± forsterite rim), (e) 1 (2%) hibonite‐bearing, spinel‐perovskite (+melilite‐pyroxene rim), (f) 1 (2%) spinel‐melilite‐pyroxene‐anorthite, and (g) 1 (2%) amoeboid olivine aggregate. Each type of CAI is known to exist in other chondrite groups, but the high abundance of pyroxene‐spinel ± melilite CAIs with igneous textures and surrounded by a forsterite rim are unique features of HH 237 and QUE 94411/94627. Additionally, oxygen isotopes consistently show relatively heavy compositions with Δ¹⁷O ranging from ?6%0 to ?10%0 (1σ = 1.3%0) for all analyzed CAI minerals (grossite, hibonite, melilite, pyroxene, spinel). This suggests that the CAIs formed in a reservoir isotopically distinct from the reservoir(s) where “normal”, ¹⁶O‐rich (Δ¹⁷O < ?20%0) CAIs in most other chondritic meteorites formed. The Al‐diopside‐rich chondrules, which have previously been observed in CH chondrites and the unique carbonaceous chondrite Adelaide, contain Al‐diopside grains enclosing oriented inclusions of forsterite, and interstitial anorthitic mesostasis and Al‐rich, Ca‐poor pyroxene, occasionally enclosing spinel and forsterite. These chondrules are mineralogically similar to the Al‐rich barred‐olivine chondrules in HH 237 and QUE 94411/94627, but have lower Cr concentrations than the latter, indicating that they may have formed during the same chondrule‐forming event, but at slightly different ambient nebular temperatures. Aluminum‐diopside grains from two Al‐diopside‐rich chondrules have O‐isotopic compositions (Δ¹⁷O ? ?7 ± 1.1 %0) similar to CAI minerals, suggesting that they formed from an isotopically similar reservoir. The oxygen‐isotopic composition of one Ca, Al‐poor cryptocrystalline chondrule in QUE 94411/94627 was analyzed and found to have Δ¹⁷O ? ?3 ± 1.4%0. The characteristics of the CAIs in HH 237 and QUE 94411/94627 are inconsistent with an impact origin of these metal‐rich meteorites. Instead they suggest that the components in CB chondrites are pristine products of large‐scale, high‐temperature processes in the solar nebula and should be considered bona fide chondrites.