Geochemistry of the ungrouped carbonaceous chondrite Tagish Lake,the anomalous CM chondrite Bells,and comparison with CI and CM chondrites

Abstract— I have determined the composition via instrumental neutron activation analysis of a bulk pristine sample of the Tagish Lake carbonaceous chondrite fall, along with bulk samples of the CI chondrite Orgueil and of several CM chondrites. Tagish Lake has a mean of refractory lithophile element/Cr ratios like those of CM chondrites, and distinctly higher than the CI chondrite mean. Tagish Lake exhibits abundances of the moderately volatile lithophile elements Na and K that are slightly higher than those of mean CM chondrites. Refractory through moderately volatile siderophile element abundances in Tagish Lake are like those of CM chondrites. Tagish Lake is distinct from CM chondrites in abundances of the most volatile elements. Mean CI‐normalized Se/Co, Zn/Co and Cs/Co for Tagish Lake are 0.68 ± 0.01, 0.71 ± 0.07 and 0.76 ± 0.02, while for all available CM chondrite determinations, these ratios lie between 0.31 and 0.61, between 0.32 and 0.58, and between 0.39 and 0.74, respectively. Considering petrography, and oxygen isotopic and elemental compositions, Tagish Lake is an ungrouped member of the carbonaceous chondrite clan. The overall abundance pattern is similar to those of CM chondrites, indicating that Tagish Lake and CMs experienced very similar nebular fractionations. Bells is a CM chondrite with unusual petrologic characteristics. Bells has a mean CI‐normalized refractory lithophile element/Cr ratio of 0.96, lower than for any other CM chondrite, but shows CI‐normalized moderately volatile lithophile element/Cr ratios within the ranges of other CM chondrites, except for Na which is low. Iridium, Co, Ni and Fe abundances are like those of CM chondrites, but the moderately volatile siderophile elements, Au, As and Sb, have abundances below the ranges for CM chondrites. Abundances of the moderately volatile elements Se and Zn of Bells are within the CM ranges. Bells is best classified as an anomalous CM chondrite.     

Lewis Cliff 85332: A unique carbonaceous chondrite

Abstract— Lewis Cliff 85332 (LEW85332) is a highly unequilibrated (type 3.0–3.1) unique carbonaceous chondrite. It resembles CI and “CR” chondrites in its abundance ratios of refractory lithophiles and refractory siderophiles, but differs significantly from these groups in important ways: relative to CI chondrites, LEW85332 has low abundances of Mn, Se, Zn and most volatile siderophiles; relative to “CR” chondrites, LEW85332 has high abundance ratios of Mn and most volatile siderophiles. Although several petrologic characteristics of LEW85332 resemble those of CO chondrites, LEW85332 differs from this group in having lower abundance ratios of refractory lithophiles and higher abundance ratios of common and volatile siderophiles. Chondrules (mean diameter of 170 μm) are smaller than those in CV and CM chondrites and bigger than those in most CO chondrites. Two melilite-rich (Åk 22) fluffy type-A refractory inclusions were observed. Weathering of LEW85332 has resulted in the formation of 6.2 vol.% limonite; 3.9 vol.% metallic Fe-Ni remains. The inferred original metallic Fe-Ni abundance (13–15 wt.%) is very high for a carbonaceous chondrite and is most similar to those of Kainsaz and Colony (both CO3). LEW85332 is a breccia: the one thin section we examined contains (a) ≥ 10 primitive carbonaceous chondrite clasts (with both C1 and C2 affinities) that contain magnetite framboids and platelets, (b) two clasts containing numerous 10-μm-size clusters of troilite grains, and (c) one clast containing small needles of schreibersite embedded in fine-grained silicate matrix. The unique nature of LEW85332 underscores the wide diversity of materials produced in the solar nebula.     

Chondrules: Precursors and interactions with the nebular gas

Abstract– Chondrule compositions suggest either ferroan precursors and evaporation, or magnesian precursors and condensation. Type I chondrule precursors include granoblastic olivine aggregates (planetary or nebular) and fine‐grained (dustball) precursors. In carbonaceous chondrites, type I chondrule precursors were S‐free, while type II chondrules have higher Fe/Mn than in ordinary chondrites. Many type II chondrules contain diverse forsteritic relicts, consistent with polymict dustball precursors. The relationship between finer and coarser grained type I chondrules in ordinary chondrites suggests more evaporation from more highly melted chondrules. Fe metal in type I, and Na and S in type II chondrules indicate high partial pressures in ambient gas, as they are rapidly evaporated at canonical conditions. The occurrence of metal, sulfide, or low‐Ca pyroxene on chondrule rims suggests (re)condensation. In Semarkona type II chondrules, Na‐rich olivine cores, Na‐poor melt inclusions, and Na‐rich mesostases suggest evaporation followed by recondensation. Type II chondrules have correlated FeO and MnO, consistent with condensation onto forsteritic precursors, but with different ratios in carbonaceous chondrites and ordinary chondrites, indicating different redox history. The high partial pressures of lithophile elements require large dense clouds, either clumps in the protoplanetary disk, impact plumes, or bow shocks around protoplanets. In ordinary chondrites, clusters of type I and type II chondrules indicate high number densities and their similar oxygen isotopic compositions suggest recycling together. In carbonaceous chondrites, the much less abundant type II chondrules were probably added late to batches of type I chondrules from different O isotopic reservoirs.     

The solar system abundances of phosphorus and titanium and the nebular volatility of phosphorus

Abstract— The bulk chemical composition of Orgueil and 25 other carbonaceous chondrites was determined by x‐ray fluorescence analysis. The sample sizes of the analyzed meteorites were in all cases 120 mg. The abundances of P and Ti in Orgueil and Ivuna were precisely determined by the standard addition method. The new P CI abundance is 926 ± 65 ppm. Excluding the low P of Ivuna and one Orgueil sample with unusual chemistry gives a CI P content of 930 ± 23 ppm. A CI abundance of 926 ppm corresponds to a P/Si wt ratio of 8.66 times 10^?3 (atomic ratio 7.85 times 10^?3). For Ti a CI content of 458 ± 18 ppm and a Ti/Si wtratio of 4.28 times 10^?3 (atomic ratio 2.51 times 10^?3) were found. A Si content of 10.69% was obtained for average CI. The new P CI abundance is 20 to 30% below earlier estimates, while the Ti CI abundance is in agreement with earlier determinations. From the results of the analyses of bulk carbonaceous chondrites it is concluded: (1) Refractory element/Mg ratios increase from CI through CM and C3O to C3V, but ratios among Al, Ca and Ti are constant, except for low Ca/Al ratios in the reduced subgroup of C3V. (2) The Si/Mg ratios are constant in all groups of carbonaceous chondrites. (3) There is a volatility related depletion of Cr and Fe, but the Cr/Fe ratios are constant. (4) The sequence of volatility related depletions of the moderately volatile elements P, Au, As, Mn, and Zn follows condensation temperatures (except for As), if in condensation calculations non‐ideal solid solution in the host phase is considered.     

Thermal metamorphism of CI and CM carbonaceous chondrites: An internal heating model

Abstract— Infrared diffuse reflectance spectra were measured for several thermally metamorphosed carbonaceous chondrites with CI-CM affinities which were recently found from Antarctica. Compared with other CI or CM carbonaceous chondrites, these Antarctic carbonaceous chondrites show weaker absorption bands near 3 μm due to hydrous minerals, and weaker absorption bands near 6.9 μm due to carbonates, interpreted as thermal metamorphic features. These absorption bands also disappear in the spectra of samples of the Murchison (CM) carbonaceous chondrite heated above 500 °C, implying that the metamorphic temperatures of the Antarctic carbonaceous chondrites considered here were higher than about 500 °C. Model calculations were performed to study thermal metamorphism of carbonaceous chondrites in a parent body internally heated by the decay of the extinct nuclide ²⁶Al. The maximum temperature of the interior of a body more than 20 km in radius is 500–700 °C for the bulk Al contents of CI and CM carbonaceous chondrites, assuming a ratio of ²⁶Al/²⁷Al = 5 × 10^?6 which has been previously proposed for an ordinary-chondrite parent body. The metamorphic temperatures experienced by the Antarctic carbonaceous chondrites considered here may be attainable by an internally heated body with an ²⁶Al/²⁷Al ratio similar to that inferred for an ordinary-chondrite parent body.     

Coolidge and Loongana 001: A new carbonaceous chondrite grouplet

Abstract— Petrographic and bulk compositional data suggest the existence of a new grouplet of carbonaceous chondrites consisting of Coolidge and Loongana 001. Coolidge is a carbonaceous chondrite find from Kansas, USA, previously considered a metamorphosed CV chondrite. Loongana 001 is a recent find from Western Australia. It has a high matrix/chondrule modal abundance ratio, 1–2 vol% refractory inclusions and high refractory lithophile abundance ratios (～1.35x CI), indicating that it is a carbonaceous chondrite. Coolidge and Loongana 001 have many compositional and petrographic similarities. They have refractory element abundances in the range of CV chondrites, significantly higher than those in the CR chondrites. They have similar volatile element abundance patterns showing low volatile element abundances relative to both CR and CV chondrites. Coolidge and Loongana 001 have similar chondrule dimensions and shapes, oxidation states and opaque mineral assemblages. They are also similar in petrologic type (3.8–4) and shock stage (S2). Although both Coolidge and Loongana 001 may be related to the CV clan, they are not CV chondrites, nor are they formed by metamorphism of a CV precursor. They are distinctly different in composition from CV chondrites and their chondrules are smaller and have a much lower abundance of coarse-grained chondrule rims. Coolidge and Loongana 001 constitute a distinct carbonaceous chondrite grouplet.     

Sulfur and selenium in chondritic meteorites

Abstract— We report here new analyses of S and Se in carbonaceous chondrites (2 CIs, 11 CMs, 6 CO3s, 7 CV3s, 2 C4s, 4 CRs, and 1 CH), 2 rumurutiites, ordinary chondrites (2 Hs, 2 Ls, and 1 LL), 3 anomalous chondrites, 3 acapulcoites, 3 lodranites, and in silicate inclusions of the Landes IAB iron meteorite. To avoid problems from inhomogeneous distribution of sulfides, the same samples that had been analysed for Se by INAA were analysed for S using a Leybold Heraeus Carbon and Sulfur Analyser (CSA 2002). With the measured CI contents of 5.41% S and 21.4 ppm Se a CI S/Se ratio of 2540 is obtained. A nearly identical S/Se ratio of 2560 ± 150 is found for carbonaceous chondrites (average of falls). The average ratio of all meteorite falls analysed in this study was 2500 ± 270. These data suggest that the new S content of Orgueil with 5.41% provides a reliable estimate for the average Solar System. The new solar system abundance of S of 4.62 × 10⁵ (atoms/10⁶ Si) is in good agreement with the solar photospheric abundance of 7.21 (log (a(H)) = E12) (Anders and Grevesse, 1989). Among the 50 analysed meteorites, 24 were finds from hot (Australia, Africa) and cold (Antarctica) deserts. Weathering effects in the carbonaceous chondrites and in one lodranite from the hot deserts resulted in losses of S, Se, Na and occasionally Ni. Sulfur is apparently more affected by weathering than Se. No losses were observed in ordinary chondrite finds and in meteorites collected in the Antarctica, except for the obvious loss of Na in the CM-chondrite Y 74662. The low S-content of 0.096% in Gibson, a lodranite, is probably not representative of this group of meteorites. Gibson is a find from the Australian desert and has lost S and also Se by weathering. Two other lodranites, finds from Antarctica, have about 2% S.     

Niobium and tantalum in carbonaceous chondrites: Constraints on the solar system and primitive mantle niobium/tantalum,zirconium/niobium,and niobium/uranium ratio

Abstract— We have determined Nb, Y, and Zr abundances in the carbonaceous chondrites Orgueil (CI), Murray (CM2), Murchison (CM2), Allende (CV3), and Karoonda (CK4), and in the eucrites, Pasamonte and Juvinas, by a recently developed spark source mass spectrometric technique using multiple ion counting (MIC‐SSMS). The abundance of Ta was determined in the same meteorites by radiochemical neutron activation analysis (RNAA). Precision of the MIC‐SSMS and RNAA techniques is ～3% and ≤ 5%, respectively. The new abundances for CI chondrites are: Nb = 0.247, Ta = 0.0142, Zr = 3.86, Y = 1.56 μg/g; or 0.699, 0.0202, 11.2, and 4.64 atoms/10⁶ Si atoms, respectively. The values agree with earlier compilations, but they are a factor of 2 more precise than earlier analyses. Trace element concentrations in the CM, CV, and CK chondrites are higher than in the CI chondrite Orgueil by about 37, 86, and 120%, respectively, in agreement with the variable absolute contents of refractory lithophile elements in different groups of carbonaceous chondrites. Of particular interest are the chondritic Nb/Ta, Zr/Nb, and Nb/U ratios, because these ratios are important tools for interpreting the chemical evolution of planetary bodies. We obtained Nb/Ta = 17.4 ± 0.5 for the carbonaceous chondrites and the Juvinas‐type eucrites investigated. Though this value is similar to previous estimates, it is much more precise. The same is true for Zr/Nb (15.5 ± 0.2) and Zr/Y (2.32 ± 0.12). In combination with recently published MIC‐SSMS U data for carbonaceous chondrites, we obtained a chondritic Nb/U ratio of 29 ± 2. Because Nb, Ta, Zr, Y, and U are refractory lithophile elements and presumably partitioned into the silicate phase of the Earth during core formation, the elemental ratios may also be used to constrain evolution of the Earth's primitive mantle and, with the more precise determinations fractionation of Nb and Ta during magmatic processes and mantle‐crust interactions, can now be interpreted with greater confidence.     

LIME silicates in amoeboid olivine aggregates in carbonaceous chondrites: Indicator of nebular and asteroidal processes

MnO/FeO ratios in olivine from amoeboid olivine aggregates (AOAs) reflect conditions of nebular condensation and can be used in concert with matrix textures to compare metamorphic conditions in carbonaceous chondrites. LIME (low‐iron, Mn‐enriched) olivine was identified in AOAs from Y‐81020 (CO3.05), Kaba (CV~3.1), and in Y‐86009 (CV3), Y‐86751 (CV3), NWA 1152 (CR/CV3), but was not identified in AOAs from Efremovka (CV3.1–3.4) or Allende (CV>3.6). According to thermodynamic models of nebular condensation, LIME olivine is stable at lower temperatures than Mn‐poor olivine and at low oxygen fugacities (dust enrichment <10× solar). Although this set of samples does not represent a single metamorphic sequence, the higher subtypes tend to have AOA olivine with lower Mn/Fe, suggesting that Mn/Fe decreases during parent body metamorphism. Y‐81020 has the lowest subtype and most forsteritic AOA olivine (Fo_>95) in our study, whereas Efremovka AOAs are slightly Fe‐rich (Fo_>92). AOA olivines from Kaba are mostly forsteritic, but rare Fe‐rich olivine precipitated from an aqueous fluid. A combination of precipitation of Fe‐rich olivine and diffusion of Fe into primary olivine grains resulted in iron‐rich compositions (Fo_97–59) in Allende AOAs. Variations from fine‐grained, nonporous matrix toward higher porosity and coarser lath‐like matrix olivine can be divided into six stages represented by (1) Y‐81020, Efremovka, NWA 1152; (2) Y‐86751 lithology B; (3) Y‐86009; (4) Kaba; (5) Y‐86751 lithology A; (6) Allende. These stages are inferred to represent general degree of metamorphism, although the specific roles of thermally driven grain growth and diffusion versus aqueous dissolution and precipitation remain uncertain.     

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.     

Clearwater East impact structure: A re‐interpretation of the projectile type using new platinum‐group element data from meteorites

Abstract— Platinum‐group element (PGE) concentrations and ratios obtained from samples of the Clearwater East impact melt have been used along with other siderophile element ratios to classify the impacting projectile as a carbonaceous chondrite. This is at odds with recent chromium isotope analyses that suggest ordinary chondrite‐type material is present. The present study reviews and reinterprets the available PGE data in the light of new PGE data from meteorites and concludes that the PGE ratios in the impact melt are most consistent with ordinary (possibly type‐L) chondrite source material, not carbonaceous chondrites. Therefore the structure was most probably formed by the impact of an asteroid composed of material similar to ordinary chondrites.     

Origin of Halogens and Nitrogen in Enstatite Chondrites

The EH and EL enstatite chondrites are the most reduced chondrite groups, having formed in nebular regions where the gas may have had high C/O and/or pH₂/pH₂O ratios. Enstatite chondrites (particularly EH) have higher CI- and Mg-normalized abundances of halogens (especially F and Cl) and nitrogen than ordinary chondrites and most groups of carbonaceous chondrites. Even relative to CI chondrites, EH and EL chondrites are enriched in F. We have found that literature values for the halogen abundance ratios in EH and EL chondrites are strongly correlated with the electronegativities of the individual halogens. We suggest that the most reactive halogens were the most efficient at forming compounds (e.g., halides) that were incorporated into EH-chondrite precursor materials. It seems plausible that, under the more-oxidizing conditions pertaining to the other chondrite groups, a larger fraction of the halogens remained in the gas. Nitrogen may have been incorporated into the enstatite chondrites as simple nitrides that did not condense under the more-oxidizing conditions in the regions where other chondrite groups formed. Literature data show that unequilibrated enstatite chondrites have light bulk N (δ ¹⁵N ≈ −20‰) compared to most ordinary (−5 to +20‰) and carbonaceous (+20 to +190‰) chondrites; this may reflect the contribution in enstatite chondrites of nitride condensates with δ¹⁵ N values close to the proposed nebular mean (~−400‰). In contrast, N in carbonaceous chondrites is mainly contained within ¹⁵N-rich organic matter. The major carrier of N in ordinary chondrites is unknown.     

Cover

Cover: Background–Orion Nebula; bottom left corner–combined elemental map in Mg (red), Ca (green), and Al Kα X–rays of a compound ultrarefractory CAI–bearing inclusion from the reduced CV3 carbonaceous chondrite Efremovka. The CAI consists of a Fluffy Type A inclusion, an ultrarefractory inclusion, and an amoeboid olivine aggregate (see paper by Ivanova et al. on p. 2107).     

A chemical sequence of macromolecular organic matter in the CM chondrites

Abstract— A new organic parameter is proposed to show a chemical sequence of organic matter in carbonaceous chondrites, using carbon, hydrogen, and nitrogen concentrations of solvent‐insoluble and high‐molecular weight organic matter (macromolecules) and the molecular abundance of solvent‐extractable organic compounds. The H/C atomic ratio of the macromolecule purified from nine CM chondrites including the Murchison, Sayama, and seven Antarctic meteorites varies widely from 0.11 to 0.72. During the H/C change of ?0.7 to ?0.3, the N/C atomic ratio remains at ?0.04, followed by a sharp decline from ?0.040 to ?0.017 between H/C ratios from ?0.3 to ?0.1. The H/CN/C sequence shows different degrees of organic matter thermal alteration among these chondrites in which the smaller H/C‐N/C value implies higher alteration levels on the meteorite parent body. In addition, solvent‐extractable organic compounds such as amino acids, carboxylic acids, and polycyclic aromatic hydrocarbons are abundant only in chondrites with macromolecular H/C values >?0.5. These organic compounds were extremely depleted in the chondrites with a macromolecular H/C value of <?0.5. Possibly, most solvent‐extractable organic compounds could have been lost during the thermal alteration event that caused the H/C ratio of the macromolecule to fall below 0.4.     

Zirconium and hafnium in meteorites

Abstract– The ratio of the two refractory trace elements zirconium (Zr) and hafnium (Hf) in meteorites has been proposed to be uniform. The most precise value available is 34.3 ± 0.2 (1σ). It was obtained by isotope dilution ICP‐MS applied to 15 chondrites, most of which were carbonaceous chondrites, and six achondrites. We reinvestigated the case and determined Zr/Hf ratios of a broad spectrum of meteoritic samples via laser ablation ICP‐MS. Our sample suite comprised 29 chondrites and five achondrites. The main objective of the study was two‐fold: we intended to verify the accuracy and precision of a relatively fast and inexpensive sample preparation method combined with expeditious laser ablation ICP‐MS techniques. Furthermore, we were looking into the possibility of systematic fine‐scale Zr/Hf variations among bulk meteoritic matter of different classes. The applied fusion technique together with laser ablation ICP‐MS turned out to be well suited to determine relative refractory trace element abundances. Absolute Zr/Hf ratios yield uncertainties of approximately 4% (1σ). As opposed to the most recent findings, we observed variable Zr/Hf ratios in different meteorites ranging from approximately 28 to approximately 38. Our value for Orgueil (CI1) is 34.0 ± 0.3 (1σ). Including literature data, we propose a solar system value of 34.1 ± 0.3. Our data also suggest that H chondrites tend to exhibit higher Zr/Hf ratios (average of 35.6 ± 0.5 [1σ]) while EL6 chondrites rather show low values (average of 30.8 ± 0.6 [1σ]). In addition to examining Zr/Hf ratios, we also explored the content of refractory major elements in different meteorite groups. Here, we found that EL6 chondrites often show very low Ca/Al ratios. The CI1 value for CaO/Al₂O₃ is 0.804. EL6 chondrites, however, display ratios as low as approximately 0.3. While the variation in Zr/Hf can be explained by fractional condensation processes in the early solar nebula, the observed low Ca/Al ratios in EL6 chondrites are probably attributable to deficits in oldhamite (CaS).     

Mineralogical characterization of Baptistina Asteroid Family: Implications for K/T impactor source

Bottke et al. [Bottke, W.F., Vokrouhlicky, D., Nesvorný, D., 2007. Nature 449, 48–53] linked the catastrophic formation of Baptistina Asteroid Family (BAF) to the K/T impact event. This linkage was based on dynamical and compositional evidence, which suggested the impactor had a composition similar to CM2 carbonaceous chondrites. However, our recent study [Reddy, V., Emery, J.P., Gaffey, M.J., Bottke, W.F., Cramer, A., Kelley, M.S., 2009. Meteorit. Planet. Sci. 44, 1917–1927] suggests that the composition of (298) Baptistina is similar to LL-type ordinary chondrites rather than CM2 carbonaceous chondrites. This rules out any possibility of it being related to the source of the K/T impactor, if the impactor was of CM-type composition. Mineralogical study of asteroids in the vicinity of BAF has revealed a plethora of compositional types suggesting a complex formation and evolution environment. A detailed compositional analysis of 16 asteroids suggests several distinct surface assemblages including ordinary chondrites (Gaffey SIV subtype), primitive achondrites (Gaffey SIII subtype), basaltic achondrites (Gaffey SVII subtype and V-type), and a carbonaceous chondrite. Based on our mineralogical analysis we conclude that (298) Baptistina is similar to ordinary chondrites (LL-type) based on olivine and pyroxene mineralogy and moderate albedo. S-type and V-type in and around the vicinity of BAF we characterized show mineralogical affinity to (8) Flora and (4) Vesta and could be part of their families. Smaller BAF asteroids with lower SNR spectra showing only a ‘single’ band are compositionally similar to (298) Baptistina and L/LL chondrites. It is unclear at this point why the silicate absorption bands in spectra of asteroids with formal family definition seem suppressed relative to background population, despite having similar mineralogy.     

Mechanisms accounting for variations in the proportions of carbonaceous and ordinary chondrites in different mass ranges

The number ratio of carbonaceous to ordinary chondrites (the CC/OC ratio) varies with mass. It is very high (≳90) in small mass ranges (10⁻⁸ to 10⁻¹² kg) among interplanetary dust particles and micrometeorites; it is moderately high (~5 to 30) for 1 to 10 m size fireball meteoroids (with estimated masses between ~10³ and ~10⁶ kg). In the range of most normal-sized meteorite falls (0.01–20 kg), the ratio is low (0.04–0.05); the ratio increases at greater mass ranges: at ≥200 kg, the ratio is 0.09; at ≥500 kg, the ratio is 0.20. The CC/OC ratio also increases from 0.05 to 0.16 for small meteorite finds (10⁻³ to 10⁻⁴ kg). High CC/OC ratios at low and high mass ranges are due to the predominance of CC material in the outer solar system. Small particles from this region spiral into the inner solar system typically in ≤10⁶ years due to Poynting–Robertson drag. Meter-sized meteoroids in this region are affected by Yarkovsky forces, pushing them into resonances where they are efficiently transferred to the inner solar system. Normal-sized meteorites are derived from centimeter-to-decimeter-sized meteoroids that have sluggish drift rates (i.e., they are less affected by the seasonal Yarkovsky effect) compared to larger bodies. Consequently, the centimeter-to-decimeter-sized meteoroids spend more time in interplanetary space (where they are subject to collisions) than larger objects. The greater friability of carbonaceous chondrites relative to ordinary chondrites tends to winnow the carbonaceous chondrites out in this size/mass range during their long interplanetary sojourn, thereby decreasing the CC/OC ratio.     

Aluminum‐26 in calcium‐aluminum‐rich inclusions and chondrules from unequilibrated ordinary chondrites

Abstract— In order to investigate the distribution of ²⁶A1 in chondrites, we measured aluminum‐magnesium systematics in four calcium‐aluminum‐rich inclusions (CAIs) and eleven aluminum‐rich chondrules from unequilibrated ordinary chondrites (UOCs). All four CAIs were found to contain radiogenic ²⁶Mg (²⁶Mg*) from the decay of ²⁶A1. The inferred initial ²⁶Al/²⁷Al ratios for these objects ((²⁶Al/²⁷Al)₀ ? 5 × 10^?5) are indistinguishable from the (²⁶Al/²⁷Al)₀ ratios found in most CAIs from carbonaceous chondrites. These observations, together with the similarities in mineralogy and oxygen isotopic compositions of the two sets of CAIs, imply that CAIs in UOCs and carbonaceous chondrites formed by similar processes from similar (or the same) isotopic reservoirs, or perhaps in a single location in the solar system. We also found ²⁶Mg* in two of eleven aluminum‐rich chondrules. The (²⁶Al/²⁷Al)₀ ratio inferred for both of these chondrules is ～1 × 10^?5, clearly distinct from most CAIs but consistent with the values found in chondrules from type 3.0–3.1 UOCs and for aluminum‐rich chondrules from lightly metamorphosed carbonaceous chondrites (～0.5 × 10^?5 to ～2 × 10^?5). The consistency of the (²⁶Al/²⁷Al)₀ ratios for CAIs and chondrules in primitive chondrites, independent of meteorite class, implies broad‐scale nebular homogeneity with respect to ²⁶Al and indicates that the differences in initial ratios can be interpreted in terms of formation time. A timeline based on ²⁶Al indicates that chondrules began to form 1 to 2 Ma after most CAIs formed, that accretion of meteorite parent bodies was essentially complete by 4 Ma after CAIs, and that metamorphism was essentially over in type 4 chondrite parent bodies by 5 to 6 Ma after CAIs formed. Type 6 chondrites apparently did not cool until more than 7 Ma after CAIs formed. This timeline is consistent with ²⁶Al as a principal heat source for melting and metamorphism.     

Perceptive of the pyroxene-bearing micrometeorites and their relation to chondrites

We studied 149 pyroxenes from 69 pyroxene-bearing micrometeorites collected from deep-sea sediments of the Indian Ocean and South Pole Water Well at Antarctica, Amundsen-Scott South Pole station. The minor elements in pyroxenes from micrometeorites are present in the ranges as follows: MnO ~0.0–0.4 wt%, Al₂O₃ ~0.0–1.5 wt%, CaO ~0.0–1.0 wt%, Cr₂O₃ ~0.3–0.9 wt%, and FeO ~0.5–4 wt%. Their chemical compositions suggest that pyroxene-bearing micrometeorites are mostly related to precursors from carbonaceous chondrites rather than ordinary chondrites. The Fe/(Fe+Mg) ratio of the pyroxenes and olivines in micrometeorites shows similarities to carbonaceous chondrites with values lying between 0 and 0.2, and those with values beyond this range are dominated by ordinary chondrites. Atmospheric entry of the pyroxene-bearing micrometeorites is expected to have a relatively low entry velocity of <16 km s⁻¹ and high zenith angle (70–90°) to preserve their chemical compositions. In addition, similarities in the pyroxene and olivine mineralogical compositions between carbonaceous chondrites and cometary particles suggest that dust in the solar system is populated by materials from different sources that are chemically similar to each other. Our results on pyroxene chemical compositions reveal significant differences with those from ordinary chondrites. The narrow range in olivine and pyroxene chemical compositions are similar to those from carbonaceous chondrites, and a small proportion to ordinary chondrites indicates that dust is largely sourced from carbonaceous chondrite-type bodies.     

The Distribution and Significance of Evaporitic Weathering Products on Antarctic Meteorites

Abstract— The distribution of white evaporitic deposits differs among different meteorite compositional groups and weathering categories of Antarctic meteorites. Evaporites occur with unusual frequency on carbonaceous chondrites, and are especially common in carbonaceous chondrites of weathering categories A and B. Among achondrites, weathering categories A and A/B show the most examples of evaporite weathering. Unlike carbonaceous chondrites and achondrites, most evaporite-bearing ordinary (H and L) chondrites are from rustier meteorites of weathering categories B and, to a lesser degree, B/C and C. LL chondrites are conspicuous by their complete lack of any evaporitic weathering product. Almost two-thirds of all evaporite-bearing meteorites belong to weathering categories A, A/B, and B. Where chemical data are available, surficial evaporite deposits are associated with elemental anomalies in meteorite interiors. Meteorites of weathering classes B, A/B, and even A may have experienced significant element redistribution and/or contamination as a result of terrestrial exposure. Evaporite formation during terrestrial weathering cannot be neglected in geochemical, cosmochemical, and mineralogical studies of Antarctic meteorites. A lower-case “e” should be added to the weathering classification of evaporite-bearing Antarctic meteorites, to inform meteorite scientists of the presence of evaporite deposits and their associated compositional effects.