Boron in chondrules

Abstract— Isotopic compositions and abundances of boron were measured in sixteen chondrules from seven chondrites by ion microprobe mass spectrometry. The chondrules are of the porphyritic, barred, and radial type and host meteorites include carbonaceous, ordinary, and enstatite chondrites. Boron abundances are generally low with average boron concentrations of between 80 and 500 ppb. These abundances are lower than those of bulk chondrites (0.35 to 1.2 ppm; Zhai et al., 1996), confirming earlier suggestions that boron is mostly contained in the matrix. No significant variation in the ¹¹B/¹⁰B ratio is observed among these chondrules, outside our experimental error limits of several permil, and B‐isotopic compositions agree with those reported for bulk chondrites. The lack of a significant isotope fractionation between chondrules and matrix implies that the low boron abundances are not the result of a Rayleigh fractionation during chondrule formation. Isotopic heterogeneities within individual chondrules are constrained to be < ±20%0 at > 95% confidence level at a spatial scale of 20–30 μm, significantly lower than the value of about ±40%0 previously reported for chondrules from carbonaceous and ordinary chondrites (Chaussidon and Robert, 1995, 1998). The observed B‐isotopic homogeneity does not conflict with the presence of decay products from extinct ¹⁰Be, with (¹⁰Be/⁹Be)₀ ? 10^?3, as was inferred for calcium‐aluminum‐rich inclusions. Extinct ¹⁰Be in chondrules would shift the abundance ratio ¹¹B/¹⁰B at best by several permil because of their commonly observed low Be/B ratios (<2). The results show that potential B‐isotopic heterogeneities in the solar nebula due to the presence of components with different B‐isotopic signatures, such as boron produced by high‐energy galactic cosmic rays (¹¹B/¹⁰B ? 2.5), or by the hypothetical low‐energy particle irradiation (¹¹B/¹⁰B ? 3.5–11) or boron from type II supernovae (¹¹B/¹⁰B >> 1), did not survive the chondrule formation processes to a measurable extent.     

Bulk Mg isotopic compositions of Ca‐Al‐rich inclusions and amoeboid olivine aggregates

Abstract— High‐precision Mg isotopic compositions of Ca‐Al‐rich inclusions (CAIs) from both Ningqiang (ungrouped) and Allende (CV3) carbonaceous chondrites and amoeboid olivine aggregations (AOAs) from Allende were analyzed by multicollector inductively coupled plasma mass spectrometry (MC‐ICP‐MS). The CAIs from Allende plot on a line, with an inferred initial ²⁶Al/²⁷Al ratio of (4.77 ± 0.39) × 10^?5 close to the canonical value. This indicates a relatively closed Al‐Mg system in the CAIs and no significant Mg isotope exchange with ambient materials, although two of the CAIs are severely altered. The AOAs contain excess ²⁶Mg and plot close to the CAI regression line, which is suggestive of their contemporary formation. The CAIs from Ningqiang define a different line with a lower inferred (²⁶Al/²⁷Al)₀ ratio of (3.56 ± 0.08) × 10^?5. None of the CAIs and AOAs studied in this work shows significant mass fractionation with enrichment of the heavier Mg isotopes, arguing against an evaporation origin.     

Light noble gases and cosmogenic radionuclides in Estherville,Budulan, and other mesosiderites: Implications for exposure histories and production rates

Abstract— We report measurements of ²⁶AI, ¹⁰Be, ⁴¹Ca, and ³⁶Cl in the silicate and metal phases of 11 mesosiderites, including several specimens each of Budulan and Estherville, of the brecciated meteorite Bencubbin, and of the iron meteorite Udei Station. Average production rate ratios (atom/atom) for metal phase samples from Estherville and Budulan are ²⁶Al/¹⁰Be = 0.77 ± 0.02; ³⁶Cl/¹⁰Be = 5.3 ± 0.2. For a larger set of meteorites that includes iron meteorites and other mesosiderites, we find ²⁶Al/¹⁰Be = 0.72 ± 0.01 and ³⁶Cl/¹⁰Be = 4.5 ± 0.2. The average ⁴¹Ca/³⁶Cl production rate ratio is 1.10 ± 0.04 for metal separates from Estherville and four small iron falls. The ⁴¹Ca activities in dpm/(kg Ca) of various silicate separates from Budulan and Estherville span nearly a factor of 4, from <400 to >1600, indicating preatmospheric radii of >30 cm. After allowance for composition, the activities of ²⁶Al and ¹⁰Be (dpm/kg silicate) are similar to values measured in most ordinary chondrites and appear to depend only weakly on bulk Fe content. Unless shielding effects are larger than suggested by the ³⁶Cl and ⁴¹Ca activities of the metal phases, matrix effects are unimportant for ¹⁰Be and minor for ²⁶Al. Noble gas concentrations and isotopic abundances are reported for samples of Barea, Emery, Mincy, Morristown, and Marjalahti. New estimates of ³⁶Cl/³⁶Ar exposure ages for the metal phases agree well with published values. Neon‐21 production rates for mesosiderite silicates calculated from these ages and from measured ²¹Ne contents are consistently higher than predicted for L chondrites despite the fact that the mesosiderite silicates have lower Mg contents than L chondrites. We suggest that the elevation of the ²¹Ne production rate in mesosiderite silicates reflects a “matrix effect,” that is, the influence of the higher Fe content of mesosiderites, which acts to enhance the flux of low‐energy secondary particles and hence the ²¹Ne production from Mg. As ¹⁰Be production is relatively insensitive to this matrix effect, ¹⁰Be/²¹Ne ages give erroneously low production rates and high exposure ages. By coincidence, standard ²²Ne/²¹Ne based “shielding” corrections give fairly reliable ²¹Ne production rates in the mesosiderite silicates.     

In situ oxygen,magnesium, and silicon isotopic compositions of the FUN inclusion Vigarano 1623-5

Oxygen, magnesium, and silicon isotopic abundances in Vigarano 1623-5 were studied using secondary ion mass spectrometry to investigate correlations between isotopic and petrologic properties of this unique forsterite-bearing FUN inclusion. Vigarano 1623-5 displays large, correlated mass-dependent fractionation effects, tightly linked to mineralogy within distinct petrologic units of the inclusion. The pyroxene-rich and melilite-rich interior parts of the inclusion display highly mass-fractionated isotopic compositions of oxygen, magnesium, and silicon, consistent with Rayleigh distillation during evaporation of a melt with initial oxygen composition close to a solar composition. However, the chemical composition, enriched in magnesium and silicon, suggests a precursor already fractionated by prior melt evaporation. A discontinuous igneous rim was produced by a flash-melting event followed by isotopic exchange in the rim melilite with planetary-like oxygen, mechanical fragmentation, and reassembly with an accretionary rim of heterogeneous materials. Al-rich minerals in 1623-5 show evidence for having crystallized with live ²⁶Al but at less than the “canonical” level of most CV calcium-aluminum-rich inclusions. However, well-defined ²⁶Al-²⁶Mg isochrons are not found and temporal implications are ambiguous.     

Campo del Cielo iron meteorite: Sample shielding and meteoroid's preatmospheric size

Abstract— Long‐lived cosmogenic radioisotopes, ¹⁰Be, ²⁶Al, ³⁶Cl, ⁴¹Ca and ⁵⁹Ni, have been measured in five samples from the Campo del Cielo iron meteorite by accelerator mass spectrometry (AMS). The ³⁶Cl activities were significantly above the background. For the concentrations of the other four radioisotopes, only upper limits were obtained that were, however, consistent with the ³⁶Cl result. The measured ³⁶Cl activity allowed an estimate of the meteoroid's preatmospheric size: a radius larger than 300 cm and a mass of at least 840 000 kg. We conclude that this meteorite might be one of the largest meteorites to have been recovered.     

The lack of potassium‐isotopic fractionation in Bishunpur chondrules

Abstract— In a search for evidence of evaporation during chondrule formation, the mesostases of 11 Bishunpur chondrules and melt inclusions in olivine phenocrysts in 7 of them have been analyzed for their alkali element abundances and K‐isotopic compositions. Except for six points, all areas of the chondrules that were analyzed had δ⁴¹K compositions that were normal within error (typically ±3%, 2s?). The six “anomalous” points are probably all artifacts. Experiments have shown that free evaporation of K leads to large ⁴¹K enrichments in the evaporation residues, consistent with Rayleigh fractionation. Under Rayleigh conditions, a 3% enrichment in δ⁴¹K is produced by ～12% loss of K. The range of L‐chondrite‐normalized K/Al ratios (a measure of the K‐elemental fractionation) in the areas analyzed vary by almost three orders of magnitude. If all chondrules started out with L‐chondrite‐like K abundances and the K loss occurred via Rayleigh fractionation, the most K‐depleted chondrules would have had compositions of up to δ⁴¹K ? 200%. Clearly, K fractionation did not occur by evaporation under Rayleigh conditions. Yet experiments and modeling indicate that K should have been lost during chondrule formation under currently accepted formation conditions (peak temperature, cooling rate, etc.). Invoking precursors with variable alkali abundances to produce the range of K/Al fractionation in chondrules does not explain the K‐isotopic data because any K that was present should still have experienced sufficient loss during melting for there to have been a measurable isotopic fractionation. If K loss and isotopic fractionation was inevitable during chondrule formation, the absence of K‐isotopic fractionation in Bishunpur chondrules requires that they exchanged K with an isotopically normal reservoir during or after formation. There is evidence for alkali exchange between chondrules and rim‐matrix in all unequilibrated ordinary chondrites. However, melt inclusions can have alkali abundances that are much lower than the mesostases of the host chondrules, which suggests that they at least remained closed since formation. If it is correct that some or all melt inclusions remained closed since formation, the absence of K‐isotopic fractionation in them requires that the K‐isotopic exchange took place during chondrule formation, which would probably require gas‐chondrule exchange. Potassium evaporated from fine‐grained dust and chondrules during chondrule formation may have produced sufficient K‐vapor pressure for gas‐chondrule isotopic exchange to be complete on the timescales of chondrule formation. Alternatively, our understanding of chondrule formation conditions based on synthesis experiments needs some reevaluation.     

Mass‐dependent fractionation of nickel isotopes in meteoritic metal

Abstract— We measured nickel isotopes via multicollector inductively coupled plasma mass spectrometry (MC‐ICPMS) in the bulk metal from 36 meteorites, including chondrites, pallasites, and irons (magmatic and non‐magmatic). The Ni isotopes in these meteorites are mass fractionated; the fractionation spans an overall range of ～0.4‰ amu^?1. The ranges of Ni isotopic compositions (relative to the SRM 986 Ni isotopic standard) in metal from iron meteorites (～0.0 to ～0.3‰ amu^?1) and chondrites (～0.0 to ～0.2‰ amu^?1) are similar, whereas the range in pallasite metal (～–0.1 to 0.0‰ amu^?1) appears distinct. The fractionation of Ni isotopes within a suite of fourteen IIIAB irons (～0.0 to ～0.3‰ amu^?1) spans the entire range measured in all magmatic irons. However, the degree of Ni isotopic fractionation in these samples does not correlate with their Ni content, suggesting that core crystallization did not fractionate Ni isotopes in a systematic way. We also measured the Ni and Fe isotopes in adjacent kamacite and taenite from the Toluca IAB iron meteorite. Nickel isotopes show clearly resolvable fractionation between these two phases; kamacite is heavier relative to taenite by ～0.4‰ amu^?1. In contrast, the Fe isotopes do not show a resolvable fractionation between kamacite and taenite. The observed isotopic compositions of kamacite and taenite can be understood in terms of kinetic fractionation due to diffusion of Ni during cooling of the Fe‐Ni alloy and the development of the Widmanstätten pattern.     

Exposure history of glass and breccia phases of lunar meteorite EET87521

Abstract— Glass-rich separates were prepared from a sample of the basaltic lunar meteorite EET87521 rich in dark glass. Noble gas isotopic abundances and ²⁶Al and ¹⁰Be activities were measured to find out whether shock effects associated with lunar launch helped to assemble these phases. Similar ¹⁰Be and ²⁶Al activities indicate that all materials in EET87521 had a common exposure history in the last few million years before launch. However, the glass contains much higher concentrations of trapped gases and records a much longer cosmic-ray exposure, 100 Ma–150 Ma, in the lunar regolith than does the bulk sample. The different histories show that the glass existed long before the ejection of EET87521. The trapped ⁴⁰Ar/³⁶Ar ratio of 1.6 ± 0.1 implies that the lunar exposure that produced most of the stable cosmogenic noble gases began 500 Ma ago. Cosmogenic and trapped noble gas components correlate strongly in various temperature-release fractions and phases of EET87521, which is probably because the glass contains most of the gas. The trapped solar ratios, ²⁰Ne/²²Ne = 12.68 ± 0.20 and ³⁶Ar/³⁸Ar = 5.24 ± 0.05 can be understood as resulting from a mixture consisting of ～60% solar wind and 40% solar energetic particles (SEP). All EET87521 phases show a ⁴⁰K-⁴⁰Ar gas retention age of ～3300 Ma, which is in the range of typical lunar mare basalts.     

Oxygen and Al‐Mg isotopic compositions of grossite‐bearing refractory inclusions from CO3 chondrites

The distribution of the short‐lived radionuclide ²⁶Al in the early solar system remains a major topic of investigation in planetary science. Thousands of analyses are now available but grossite‐bearing Ca‐, Al‐rich inclusions (CAIs) are underrepresented in the database. Recently found grossite‐bearing inclusions in CO3 chondrites provide an opportunity to address this matter. We determined the oxygen and magnesium isotopic compositions of individual phases of 10 grossite‐bearing CAIs in the Dominion Range (DOM) 08006 (CO3.0) and DOM 08004 (CO3.1) chondrites. All minerals in DOM 08006 CAIs as well as hibonite, spinel, and pyroxene in DOM 08004 are uniformly ¹⁶O‐rich (Δ¹⁷O = ?25 to ?20‰) but grossite and melilite in DOM 08004 CAIs are not; Δ¹⁷O of grossite and melilite range from ~ ?11 to ~0‰ and from ~ ?23 up to ~0‰, respectively. Even within this small suite, in the two chondrites a bimodal distribution of the inferred initial ²⁶Al/²⁷Al ratios (²⁶Al/²⁷Al)₀ is seen, with four having (²⁶Al/²⁷Al)₀ ≤1.1 × 10^?5 and six having (²⁶Al/²⁷Al)₀ ≥3.7 × 10^?5. Five of the ²⁶Al‐rich CAIs have (²⁶Al/²⁷Al)₀ within error of 4.5 × 10^?5; these values can probably be considered indistinguishable from the “canonical” value of 5.2 × 10^?5 given the uncertainty in the relative sensitivity factor for grossite measured by secondary ion mass spectrometry. We infer that the ²⁶Al‐poor CAIs probably formed before the radionuclide was fully mixed into the solar nebula. All minerals in the DOM 08006 CAIs, as well as spinel, hibonite, and Al‐diopside in the DOM 08004 CAIs retained their initial oxygen isotopic compositions, indicating homogeneity of oxygen isotopic compositions in the nebular region where the CO grossite‐bearing CAIs originated. Oxygen isotopic heterogeneity in CAIs from DOM 08004 resulted from exchange between the initially ¹⁶O‐rich (Δ¹⁷O ~?24‰) melilite and grossite and ¹⁶O‐poor (Δ¹⁷O ~0‰) fluid during hydrothermal alteration on the CO chondrite parent body; hibonite, spinel, and Al‐diopside avoided oxygen isotopic exchange during the alteration. Grossite and melilite that underwent oxygen isotopic exchange avoided redistribution of radiogenic ²⁶Mg and preserved undisturbed internal Al‐Mg isochrons. The Δ¹⁷O of the fluid can be inferred from O‐isotopic compositions of aqueously formed fayalite and magnetite that precipitated from the fluid on the CO parent asteroid. This and previous studies suggest that O‐isotope exchange during fluid–rock interaction affected most CAIs in CO ≥3.1 chondrites.     

SODIUM-22, 26AI,AND 10Be IN 3He-RICH FLARES

The theory of ³He-rich flares by Colgate, Audouze, and Fowler implies that the composition of the solar cosmic ray-event associated with a ³He-rich flare is grossly non-solar. The relative abundances (relative to hydrogen) of carbon, nitrogen, and oxygen, as well as those of heavier elements are significantly reduced, and the isotopic compositions of virtually all elements are bound to be strongly anomalous. In addition, the abundances of ²²Na, ²⁶Al, and ¹⁰Be (of which there are approximately 10²⁵atoms each in a ³He-rich flare) are at least comparable to the abundances of stable isotopes of these elements. Conditions for the detectability of the three radioactive species are discussed.     

Al‐Mg systematics of hibonite‐bearing Ca,Al‐rich inclusions from Ningqiang

Abstract– Hibonite‐bearing Ca,Al‐rich inclusions (CAIs) usually occur in CM and CH chondrites and possess petrographic and isotopic characteristics distinctive from other typical CAIs. Despite their highly refractory nature, most hibonite‐bearing CAIs have little or no ²⁶Mg excess (the decay product of ²⁶Al), but do show wide variations of Ca and Ti isotopic anomalies. A few spinel‐hibonite spherules preserve evidence of live ²⁶Al with an inferred ²⁶Al/²⁷Al close to the canonical value. The bimodal distribution of ²⁶Al abundances in hibonite‐bearing CAIs has inspired several interpretations regarding the origin of short‐lived nuclides and the evolution of the solar nebula. Herein we show that hibonite‐bearing CAIs from Ningqiang, an ungrouped carbonaceous chondrite, also provide evidence for a bimodal distribution of ²⁶Al. Two hibonite aggregates and two hibonite‐pyroxene spherules show no ²⁶Mg excesses, corresponding to inferred ²⁶Al/²⁷Al < 8 × 10^?6. Two hibonite‐melilite spherules are indistinguishable from each other in terms of chemistry and mineralogy but have different Mg isotopic compositions. Hibonite and melilite in one of them display positive ²⁶Mg excesses (up to 25‰) that are correlated with Al/Mg with an inferred ²⁶Al/²⁷Al of (5.5 ± 0.6) × 10^?5. The other one contains normal Mg isotopes with an inferred ²⁶Al/²⁷Al < 3.4 × 10^?6. Hibonite in a hibonite‐spinel fragment displays large ²⁶Mg excesses (up to 38‰) that correlate with Al/Mg, with an inferred ²⁶Al/²⁷Al of (4.5 ± 0.8) × 10^?5. Prolonged formation duration and thermal alteration of hibonite‐bearing CAIs seem to be inconsistent with petrological and isotopic observations of Ningqiang. Our results support the theory of formation of ²⁶Al‐free/poor hibonite‐bearing CAIs prior to the injection of ²⁶Al into the solar nebula from a nearby stellar source.     

Cross sections from 5 to 35 MeV for the reactions natMg(3He,x)26Al, 27Al(3He,x)26Al,natCa(3He,x)41Ca,and natCa(3He,x)36Cl: Implications for early irradiation in the solar system

Abstract– Cross sections were measured for the nuclear reactions ^natMg(³He,x)²⁶Al, ²⁷Al(³He,x)²⁶Al, ^natCa(³He,x)⁴¹Ca, and ^natCa(³He,x)³⁶Cl in the energy region from approximately 5–35 MeV. The rates of these reactions are important for studies of early solar system irradiation scenarios. The ²⁶Al, ³⁶Cl, and ⁴¹Ca were separated chemically, and the numbers of atoms produced in each reaction channel were measured using accelerator mass spectrometry (AMS). From these results, 26 cross sections were determined and compared with predictions of the TALYS code. Agreement is within 40% for most cross sections. Our measurements were used to model the production of ⁷Be, ¹⁰Be, ²⁶Al, and ⁴¹Ca in the early solar system. For projectiles ¹H, ³He, and ⁴He, we assumed energy spectra of the general form E^?α. For a wide range of parameterizations, the modeled ratios of ⁷Be/Be and ¹⁰Be/Be on the one hand and of ²⁶Al/²⁷Al and ⁴¹Ca/Ca on the other are coupled because the excitation functions for the relevant nuclear reactions have similar shapes. Modeling of a closed system with the constraint that ¹⁰Be/⁹Be = 0.001 fails to reproduce simultaneously the range of ⁷Be/⁹Be, ²⁶Al/²⁷Al, and ⁴¹Ca/Ca ratios inferred for the early solar system from studies of meteorites.     

Chemical and oxygen isotopic properties of ordinary chondrites (H5, L6) from Oman: Signs of isotopic equilibrium during thermal metamorphism

Mean bulk chemical data of recently found H5 and L6 ordinary chondrites from the deserts of Oman generally reflect isochemical features which are consistent with the progressive thermal metamorphism of a common, unequilibrated starting material. Relative differences in abundances range from 0.5–10% in REE (Eu = 14%), 6–13% in siderophile elements (Co = 48%), and >10% in lithophile elements (exceptions are Ba, Sr, Zr, Hf, U = >30%) between H5 and L6 groups. These differences may have accounted for variable temperature conditions during metamorphism on their parent bodies. The CI/Mg‐normalized mean abundances of refractory lithophile elements (Al, Ca, Sm, Yb, Lu, V) show no resolvable differences between H5 and L6 suggesting that both groups have experienced the same fractionation. The REE diagram shows subtle enrichment in LREE with a flat HREE pattern. Furthermore, overall mean REE abundances are ~0.6 × CI with enriched La abundance (~0.9 × CI) in both groups. Precise oxygen isotope compositions demonstrate the attainment of isotopic equilibrium by progressive thermal metamorphism following a mass‐dependent isotope fractionation trend. Both groups show a ~slope‐1/2 line on a three‐isotope plot with subtle negative deviation in ?¹⁷O associated with δ¹⁸O enrichment relative to δ¹⁷O. These deviations are interpreted as the result of liberation of water from phyllosilicates and evaporation of a fraction of the water during thermal metamorphism. The resultant isotope fractionations caused by the water loss are analogous to those occurring between silicate melt and gas phase during CAI and chondrule formation in chondrites and are controlled by cooling rates and exchange efficiency.     

Magnesium isotopic fractionation in chondrules from the Murchison and Murray CM2 carbonaceous chondrites

We present high‐precision measurements of the Mg isotopic compositions of a suite of types I and II chondrules separated from the Murchison and Murray CM2 carbonaceous chondrites. These chondrules are olivine‐ and pyroxene‐rich and have low ²⁷Al/²⁴Mg ratios (0.012–0.316). The Mg isotopic compositions of Murray chondrules are on average lighter (δ²⁶Mg ranging from ?0.95‰ to ?0.15‰ relative to the DSM‐3 standard) than those of Murchison (δ²⁶Mg ranging from ?1.27‰ to +0.77‰). Taken together, the CM2 chondrules exhibit a narrower range of Mg isotopic compositions than those from CV and CB chondrites studied previously. The least‐altered CM2 chondrules are on average lighter (average δ²⁶Mg = ?0.39 ± 0.30‰, 2SE) than the moderately to heavily altered CM2 chondrules (average δ²⁶Mg = ?0.11 ± 0.21‰, 2SE). The compositions of CM2 chondrules are consistent with isotopic fractionation toward heavy Mg being associated with the formation of secondary silicate phases on the CM2 parent body, but were also probably affected by volatilization and recondensation processes involved in their original formation. The low‐Al CM2 chondrules analyzed here do not exhibit any mass‐independent variations in ²⁶Mg from the decay of ²⁶Al, with the exception of two chondrules that show only small variations just outside of the analytical error. In the case of the chondrule with the highest Al/Mg ratio (a type IAB chondrule from Murchison), the lack of resolvable ²⁶Mg excess suggests that it either formed >1 Ma after calcium‐aluminum‐rich inclusions, or that its Al‐Mg isotope systematics were reset by secondary alteration processes on the CM2 chondrite parent body after the decay of ²⁶Al.     

Mineralogical and chemical composition and cosmic‐ray exposure history of two mesosiderites and two iron meteorites

Abstract— We performed a comprehensive study of the noble gas isotopic abundances, radionuclide activities, and mineralogical and chemical composition of two mesosiderites and two iron meteorites. For the mesosiderites Dong Ujimqin Qi and Weiyuan, the silicate and the metal phases were studied. The anomalous ataxite Rafrüti is not chemically related to any other meteorite class, whereas Ningbo is a type IVA octahedrite. The mineralogy and major and trace element abundances of the silicate phases of Dong Ujimqin Qi and Weiyuan are similar to those of other mesosiderites and distinct from those of the howardites. The cosmic‐ray exposure history was studied based on the concentrations of the cosmogenic noble gas nuclei and radionuclide activities. For the iron meteorites, cosmic‐ray exposure ages were calculated from the pairs ¹⁰Be‐²¹Ne, ²⁶Al‐²¹Ne, and ³⁶Cl‐³⁶Ar. Rafrüti yields the youngest exposure age of all ataxites (6.8 ± 1.7 Ma), whereas that of Ningbo with 107 ± 15 Ma falls within the range observed for the other octahedrites. The parent body break‐up times of the mesosiderites Dong Ujimqin Qi and Weiyuan are 252 ± 50 and 25.9 ± 5.0 Ma, respectively. We find no evidence for a common break‐up event for the mesosiderites and the howardites.     

3‐D elemental and isotopic composition of presolar silicon carbides

Abstract— Thirteen presolar silicon carbide grains—three of supernova (SN) origin and ten of asymptotic giant branch (AGB) star origin—were examined with time‐of‐flight‐secondary ion mass spectrometry (TOF‐SIMS). The grains had been extracted from two different meteorites—Murchison and Tieschitz—using different acid residue methods. At high lateral resolution of ～300 nm, isotopic and elemental heterogeneities within the micrometer‐sized grains were detected. The trace elemental abundances, when displayed in two‐element correlation plots, of Li, Mg, K, and Ca show a clear distinction between the two different meteoritic sources. The different concentrations might be attributed to differences of the host meteorites and/or of extraction methods whereas the stellar source seems to be less decisive. In one SN grain with ²⁶Mg‐enrichment from extinct ²⁶Al, the acid treatment, as part of the grain separation procedure, affected the Mg/Al ratio in the outer rim and therefore the inferred initial ²⁶Al/²⁷Al ratio. A second SN grain exhibits a lateral heterogeneity in ²⁶Al/²⁷Al, which either is due to residual Al‐rich contamination on the grain surface or to the condensation chemistry in the SN ejecta.     

Short‐lived radioactivity in the early solar system: The Super‐AGB star hypothesis

Abstract– The composition of the most primitive solar system condensates, such as calcium‐aluminum‐rich inclusions (CAIs) and micron‐sized corundum grains, show that short‐lived radionuclides (SLR), e.g., ²⁶Al, were present in the early solar system. Their abundances require a local or stellar origin, which, however, is far from being understood. We present for the first time the abundances of several SLR up to ⁶⁰Fe predicted from stars with initial mass in the range approximately 7–11 M_⊙. These stars evolve through core H, He, and C burning. After core C burning they go through a “Super”‐asymptotic giant branch (Super‐AGB) phase, with the H and He shells activated alternately, episodic thermal pulses in the He shell, a very hot temperature at the base of the convective envelope (approximately 10⁸ K), and strong stellar winds driving the H‐rich envelope into the surrounding interstellar medium. The final remnants of the evolution of Super‐AGB stars are mostly O–Ne white dwarfs. Our Super‐AGB models produce ²⁶Al/²⁷Al yield ratios approximately 0.02–0.26. These models can account for the canonical value of the ²⁶Al/²⁷Al ratio using dilutions with the solar nebula of the order of 1 part of Super‐AGB mass per several 10² to several 10³ of solar nebula mass, resulting in associated changes in the O‐isotope composition in the range Δ¹⁷O from 3 to 20‰. This is in agreement with observations of the O isotopic ratios in primitive solar system condensates, which do not carry the signature of a stellar polluter. The radionuclides ⁴¹Ca and ⁶⁰Fe are produced by neutron captures in Super‐AGB stars and their meteoritic abundances are also matched by some of our models, depending on the nuclear and stellar physics uncertainties as well as the meteoritic experimental data. We also expect and are currently investigating Super‐AGB production of SLR heavier than iron, such as ¹⁰⁷Pd.     

Re-Os isotope systematics and fractionation of siderophile elements in metal phases from CBa chondrites

We report Os isotope compositions of metal grains in two CB_a chondrites (Bencubbin and Gujba) determined using a micromilling sampling coupled with thermal ionization mass spectrometry, together with the abundances of major and trace siderophile elements obtained by electron probe microanalysis and femtosecond laser ablation inductively coupled plasma–mass spectrometry. The CB_a metal grains presented ¹⁸⁷Os/¹⁸⁸Os ratios akin to carbonaceous chondrites with limited variations (0.1257–0.1270). Most of the CB_a metal grains were scattered along a ¹⁸⁷Re-¹⁸⁷Os reference isochron of IIIAB iron meteorites, indicating that the CB_a metals experienced limited Re-Os fractionation at the time of their formation. The Re/Os ratios of sampling spots for the CB_a metals, recast from the observed ¹⁸⁷Os/¹⁸⁸Os ratios, had a positive correlation with their Os/Ir ratios. In addition, the metal grains showed a positive correlation in a Pd/Fe versus Ni/Fe diagram. These correlations suggest that the CB_a metal grains have formed via equilibrium condensation or evaporation from a gaseous reservoir at ~10⁻⁴ bar with enhanced metal abundances. Compared to the Bencubbin metals, the Gujba metals are characterized by having systematically lower Pd/Fe and Ni/Fe ratios that span subchondritic values. Such a difference was most likely induced by the compositionally heterogeneous impact plume from which the metals were condensed.     

Evidence for common breakup events of the acapulcoites‐lodranites and chondrites

Abstract— Acapulcoites and lodranites are believed to originate on a common parent body and to represent some of the earliest events in the differentiation of the chondritic asteroids. We have conducted isotopic studies of the noble gases He, Ne, Ar, Kr, and Xe, and determinations of the concentrations of the major elements and of the radionuclides ¹⁰Be, ²⁶Al, and ³⁶Cl in an attempt to constrain the cosmic‐ray exposure history of two members of the acapulcoite‐lodranite clan recovered in Antarctica: Frontier Mountain (FRO) 95029 and Graves Nunataks (GRA) 95209. From cosmic‐ray‐produced ³He, ²¹Ne, and ³⁸Ar and appropriate production rates, we derive parent‐body breakup times of 4.59 ± 0.60 and 6.82 ± 0.60 Ma for FOR 95029 and GRA 95209, respectively. These times are consistent with those obtained from the pairs ¹⁰Be‐²¹Ne and ²⁶Al‐²¹Ne; whereas the times inferred from the pair ³⁶Cl‐³⁶Ar are slightly longer, perhaps because the ³⁶Cl activities decreased as a result of decay on Earth. Terrestrial ages up to ～50 ka for the two meteorites are consistent with the measured ³⁶Cl activities of the metal phases. All acapulcoites and lodranites dated until now show cosmic‐ray exposure ages in the range of 4–10 Ma. This is the same range as that found for the major exposure age cluster of the H chondrites. As a common parent body is improbable on the basis of the O‐isotopic systematics, a common set of impactors might have affected the asteroid belt 4–10 Ma ago.     

Lithium isotopes and light lithophile element abundances in shergottites: Evidence for both magmatic degassing and subsolidus diffusion

Degassed magmatic water was potentially the major source of surficial water on Mars. We measured Li, B, and Be abundances and Li isotope profiles in pyroxenes, olivines, and maskelynite from four compositionally different shergottites—Shergotty, QUE 94201, LAR 06319, and Tissint—using secondary ion mass spectrometry (SIMS). All three light lithophile elements (LLE) are incompatible: Li and B are soluble in H₂O‐rich fluids, whereas Be is insoluble. In the analyzed shergottites, Li concentration decreases and Be concentration increases from cores to rims in pyroxenes. However, B concentrations do not vary consistently with Li and Be abundances, except in QUE 94201 pyroxenes. Additionally, abundances of these three elements in olivines show a normal igneous‐fractionation trend consistent with the crystallization of olivine before magma ascent and degassing. We expect that kinetic effects would lead to fractionation of ⁶Li in the vapor phase compared to ⁷Li during degassing. The Li isotope profiles, with increasing δ⁷Li from cores to rims, as well as Li and B profiles indicate possible degassing of hydrous fluids only for the depleted shergottite QUE 94201, as also supported by degassing models. Conversely, Shergotty, LAR 06319, and Tissint appear to have been affected by postcrystallization diffusion, based on their LLE and Li isotope profiles, accompanied by diffusion models. This process may represent an overlay on a degassing pattern. The LLE profiles and isotope profiles in QUE 94201 support the hypothesis that degassing of some basaltic shergottite magmas provided water to the Martian surface, although evidence may be obscured by subsolidus diffusion processes.