Isotope anomalies in tellurium and palladium from Allende nanodiamonds

Abstract— ‐The elemental and isotopic abundances of Te and Pd have been measured by thermal ionization mass spectrometry in a purified sample of interstellar nanodiamonds from the Allende meteorite, after combustion of the diamonds in an oxygen plasma. Small positive anomalies were found in ¹²⁸Te (4.0 ± 1.5 %0) and ¹³⁰Te (9.3 ± 2.8 %0) from three analyses of the Allende nanodiamond sample EB, and in ¹¹⁰Pd (9.4 ± 5.7 %0) from two analyses of the same sample. No other anomalies of a significant nature were found in either Te or Pd. These results are consistent with the neutron burst model (Meyer et al., 2000), and the r‐process based rapid separation model of Ott (1996) in that ^{128, 130}Te and ¹¹⁰Pd are enhanced relative to their solar abundances. However, in the framework of the neutron burst model, some separation between stable products and radioactive precursors may be required in order to be consistent with the full data set of Te isotopes. In the framework of the rapid separation scenario, our data suggests a separation time of approximately 4000 s, based on the magnitudes of the precursor life‐times for ¹²⁸Te and ¹³⁰Te. The elemental abundance ratio Te‐H/Xe‐H agrees with the prediction of the rapid separation model, provided little fractionation occurred during trapping of the exotic components by the diamonds, but differs significantly from expectations based on the neutron burst model. Differences in the inferred ¹²⁸Te/¹³⁰Te ratio between our work and that of Richter et al. (1998) point to the need for further investigations.     

Search for extractable fullerenes in the Allende meteorite

Abstract— In an effort to confirm earlier observations of fullerenes in the Allende meteorite by Becker et al. (1994), we have treated nine separate whole-rock chips of this meteorite with toluene to search for extractable C₆₀ and C₇₀ fullerenes. The analysis was done with high performance liquid chromatography. Less than 1 ppb C₆₀ and C₇₀ were detected in a total of 131.82 g of this meteorite. Becker et al. (1994) have estimated a content of 100 ppm in one Allende sample. Either they have grossly overestimated the C₆₀ content of their sample, or Allende is very inhomogeneous concerning fullerenes.     

CONSTRAINTS ON CHONDRULE ORIGIN FROM PETROLOGY OF ISOTOPICALLY CHARACTERIZED CHONDRULES IN THE ALLENDE METEORITE

Petrographic and chemical features of Allende ferromagnesian chondrules previously analyzed for oxygen and silicon isotopes by Clayton et al. (1983a) provide additional information on chondrule origin. Allende, like other carbonaceous chondrites, contains two chondrule populations, but one of these is represented by only one chondrule in this isotopically characterized set. All Allende chondrules fall along an isotopic mixing line, probably defined by an ¹⁶O-rich solid component and an isotopically heavier oxygen gaseous exchange component. Differences in the amounts of isotopic exchange for porphyritic and barred chondrules presumably resulted from varying degrees of melting. Those porphyritic chondrules containing abundant relict grains experienced the least isotopic exchange. Chondrules with high bulk FeO/(FeO + MgO) ratios apparently persisted longer as liquids and contain more of the exchange component. The distinct directions of oxygen isotopic exchange in chondrules from carbonaceous, ordinary, and enstatite chondrites indicate that each formed from different solid precursor materials. Silicon isotopic variations in Allende chondrules probably reflect evaporative loss of lighter isotopes; however, silicon loss is also controlled by chondrule sizes, which are unknown. Observed correlations point to the importance of kinetic factors in a gaseous nebula for chondrule genesis, and are not consistent with models that explain chondrules as mixtures of several solids with distinct oxygen and silicon isotopic compositions.     

Axtell,a new CV3 chondrite find from Texas

Abstract— We describe a previously unreported meteorite found in Axtell, Texas, in 1943. Based on the mineralogical composition and texture of its matrix and the sizes and abundance of chondrules, we classify it as a CV3 carbonaceous chondrite. The dominant opaque phase in the chondrules is magnetite, and that in refractory inclusions is Ni-rich NiFe metal (awaruite). Axtell, therefore, belongs to the oxidized subgroup of CV3 chondrites, although unlike Allende it escaped strong sulfidation. The meteorite bears a strong textural resemblance to Allende, and its chondrule population and matrix appear to be quite similar to those of Allende, but its refractory inclusions, thermoluminescence properties, and cosmogenic ⁶⁰Co abundances are not. Our data are consistent with a terrestrial age for Axtell of ～100 years and a metamorphic grade slightly lower than that of Allende.     

Production rates and proton‐induced production cross sections of 129I from Te and Ba: An attempt to model the 129I production in stony meteoroids and 129I in a Knyahinya sample

Abstract— Proton‐induced production cross sections of ¹²⁹I from Te and Ba are presented. Earlier assumptions that Te is the most important target element in meteoroids are confirmed. Based on this data set and the experimental production rates of ¹²⁹I from thick‐target experiments, the production of ¹²⁹I in stony meteoroids is modeled using a GCR flux density of 4.06 cm^?2 s^?1. The results of this modeling must be considered preliminary because the contribution from neutron capture on ¹²⁸Te needs further investigation. We obtained modeled production rates that agree with experimental results for samples from two medium‐sized meteorites (Abee and Knyahinya). However, we find that this model does not describe ⁴¹Ca in lunar rocks well and seems to overestimate ¹²⁹I production in larger bodies, such as Allende. We present elemental production rates from Te and Ba based on our modeling as well as for a model that describes neutron capture products. For ¹²⁹I analysis of Knyahinya, a novel method to separate Te and analysis using ICP‐MS was used, enabling the use of experimental elemental concentrations obtained from the same meteorite to calculate ¹²⁹I production.     

Infrared,ultraviolet, and electron paramagnetic resonance measurements on presolar diamonds: Implications for optical features and origin

Abstract— Infrared (IR) and ultraviolet (UV) absorption spectra were obtained for diamonds from the Allende and Murchison meteorites. In addition, and for the first time, electron paramagnetic resonance spectra were measured. The IR and UV data confirm the suspicion of Russell et al. (1996) that N in presolar diamonds predominantly appears in the form of dispersed N atoms, as is the case for terrestrial type Ib diamonds. In accordance with other observations, our electron paramagnetic resonance measurements suggest a high H content in presolar diamonds. The presolar diamonds most likely originated in a H‐rich region, an environment in which nanometer‐sized diamonds may be more stable than graphite (Badziag et al., 1990). This adds to the evidence—previously based mainly on the twin microstructures of presolar diamonds (Daulton et al., 1996) and the absence of graphite with the same isotopic composition as presolar diamonds (Anders and Zinner, 1993)—for a homogeneous nucleation of presolar diamonds from a gas phase. Based on our results for detection of diamonds in space, we suggest searching for the N‐induced IR and UV absorption features of type Ib diamonds. Other characteristic diamond features that could also be used to detect diamonds in space are the (‐CH_n) IR absorption features due to H‐coated diamonds, as they are described by Allamandola et al. (1993) and the IR multiphonon absorption features of the diamond lattice. The multiphonon features are very weak (Edwards, 1985), but their intensity increases somewhat with increasing temperature (Collins and Fan, 1954), so perhaps a search for them is not totally hopeless.     

A numerical model for isotopic patterns from thermal-extraction experiments

Abstract— A model based on volume diffusion is proposed to describe thermal extraction (progressive or stepped vacuum-pyrolysis or combustion) experimental results (yield and isotopic composition), reported against time or temperature. It accounts for the common asymmetrical shape of the release patterns, with peak-tails due to the extraction kinetics. By analogy to this model, a simulation function is introduced which allows calculation of the concentration and isotopic patterns resulting from component mixings during such experiments. In this calculation, each component's isotopic composition is assumed to be constant throughout its extraction. The simulation readily explains the shift between the isotopic composition peaks and the concentration peaks in the temperature release pattern commonly observed during pyrolysis or combustion of meteorite samples. Because of its simplicity, the principles of the simulation can be easily applied by the readers to real data. One example is taken from the meteoritic stable isotope literature: the progressive pyrolysis extraction of hydrogen from the Parnallee LL3 meteorite (Robert et al., 1987a). The simulation permits calculation of a range for the isotopic composition of a D-depleted reservoir in this meteorite: ?460 < δD < ?320‰ rel. SMOW.     

Complexly zoned chromium‐aluminum spinel found in situ in the Allende meteorite

Abstract— In addition to the Mg‐, Al‐, ¹⁶O‐rich spinels that are known to occur in refractory inclusions, the Murchison meteorite contains Cr‐rich, ¹⁶O‐poor spinels, most of whose sources are unknown because they are rarely found in situ. Here we report the in situ occurrence in Allende of Cr‐rich spinels, found in 13 chondrules and 4 “olivine‐rich objects”. The Allende spinels exhibit major and minor element contents, isotopic compositions, and zoning of Cr₂O₃ contents like those of the Cr‐spinels from Murchison. Some chondrules contain patchy‐zoned spinel (Simon et al., 1994), which suggests that such grains did not form by sintering but perhaps by formation of overgrowths on relic grains. Unlike the olivine‐rich objects, phases in all three chondrules that were analyzed by ion microprobe have uniform, near‐normal O‐isotopic compositions. One olivine‐rich object, ALSP1, has a huge (1 mm) fragment of chevron‐zoned spinel. This spinel has near‐normal O‐isotopic compositions that are quite distinct from those of adjacent forsteritic olivine, which are relatively ¹⁶O‐rich and plot on the calcium‐aluminum‐inclusion (CAI) line, like some isolated forsterite grains found in Allende. The spinel and olivine in this object are therefore not genetically related to each other. Another olivine‐rich object, ALSP11A, contains a rectangular, 150 ×s 100 μm, homogeneous spinel grain with 50 wt% Cr₂O₃ and 23 wt% FeO in a vuggy aggregate of finer‐grained (5–90 μm), FeO‐rich (Fo_47–55) olivine. The magnesian core of one olivine grain has a somewhat ¹⁶O‐rich isotopic composition like that of the large spinel, whereas the FeO‐rich olivine is relatively ¹⁶O‐poor. The composition of the spinel in ALSP11A plots on the CAI line, the first Cr‐rich spinel found to do so. Chevron‐zoned spinel has not been observed in chondrules, and it is unlikely that either ALSP1 or ALSP11A were ever molten. Calculations show that a spinel with the composition of that in ALSP1 can condense at 1780 K at a P^tot of 10^?3 atm and a dust/gas ratio of 100 relative to solar. The Cr‐rich spinel in ALSP11A could condense at ～1420 K, but this would require a dust/gas enrichment of 1000 relative to solar. The data presented here confirm that, as in Murchison, the coarse Cr‐rich spinels in Allende are relatively ¹⁶O‐depleted and are isotopically distinct from the ¹⁶O‐enriched MgAl₂O₄ from CAIs. Sample ALSP11A may represent a third population, one that is Cr‐rich and plots on the CAI line. That the O‐isotopic composition of ALSP1 is like those of Cr‐rich spinels from chondrules indicates that O‐isotopic compositions cannot be used to distinguish whether grains from such unequilibrated objects are condensates or are fragments from a previous generation of chondrules.     

Nuclear field shift effect as a possible cause of Te isotopic anomalies in the early solar system—An alternative explanation of Fehr et al. (2006 and 2009)

Abstract— We explore the possibility that Te isotopic anomalies measured in Ca‐Al‐rich inclusions (Fehr et al. 2009) and in leachates of carbonaceous chondrites (Fehr et al. 2006) may be due to mass‐independent effects controlled by nuclear field shift rather than to nucleosynthetic processes. Fehr et al.'s spectrum of mass‐independent anomalies of Te isotopes shows a smooth correlation with mass number and nuclear charge distribution. Ratios of even to odd isotopes, as the ¹²⁵Te/¹²⁶Te ratio used by these authors for normalization are particularly prone to nuclear field shift effects. We show that the alternative normalization of isotopic ratios to ¹³⁰Te/¹²⁶Te strongly reduces the trend of isotopic fractionation with mass number, leaving only ¹²⁵Te as truly anomalous. For both normalizations (¹²⁵Te/¹²⁶Te and ¹³⁰Te/¹²⁶Te), Fehr et al.'s results fit the theory of Bigeleisen (1996), which suggests that the nuclear field shift effect can potentially account for the observed Te isotope abundances, as an alternative to nucleosynthetic processes. We propose that these mass‐independent effects may be acquired during accretion of sulfides from the solar nebula.     

Fullerenes, fulleranes and polycyclic aromatic hydrocarbons in the Allende meteorite

In this paper, we confirm our earlier observations of fullerenes (C60 and C70) in the Allende meteorite (Becker et al., 1994a, 1995). Fullerene C60 was also detected in two separate C-rich (approximately 0.5-1.0%) dark inclusions (Heymann et al., 1987) that were hand picked from the Allende sample. The amounts of C60 detected were approximately 5 and approximately 10 ppb, respectively, which is considerably less than what was detected in the Allende 15/21 sample (approximately 100 ppb; Becker et al., 1994a, 1995). This suggests that fullerenes are heterogeneously distributed in the meteorite. In addition, we present evidence for fulleranes, (C60Hx), detected in separate samples by laser desorption (reflectron) time-of-flight (TOF) mass spectrometry (LDMS). The LDMS spectra for the Allende extracts were remarkably similar to the spectra generated for the synthetic fullerane mixtures. Several fullerane products were synthesized using a Rh catalyst (Becker et al., 1993a) and separated using high-performance liquid chromatography (HPLC). Polycyclic aromatic hydrocarbons (PAHs) were also observed ppm levels) that included benzofluoranthene and corannulene, a cup-shaped molecule that has been proposed as a precursor molecule to the formation of fullerenes in the gas phase (Pope et al., 1993).     

Abundance and isotopic composition of noble gases in metal and graphite of the Bohumilitz IAB iron meteorite

Abstract— Abundances and isotopic compositions of noble gases in metal and graphite of the Bohumilitz IAB iron meteorite were measured. The abundance ratios of spallogenic components in metal reveal a ³He deficiency which is due to the diffusive loss of parent isotopes, that is, tritium (Tilles, 1963; Schultz, 1967). The diffusive loss likely has been induced by thermal heating by the Sun during cosmic‐ray exposure (～160 Ma; Lavielle et al, 1999). Thermal process such as impact‐induced partial loss may have affected the isotopic composition of spallogenic Ne. The ¹²⁹Xe/¹³¹Xe ratio of cosmogenic components in the metal indicates an enhanced production of epi‐thermal neutrons. The abundance ratios of spallogenic components in the graphite reveal that it contained small amounts of metal and silicates. The isotopic composition of heavy noble gases in graphite itself was obtained from graphite treated with HF/HCl. The isotopic composition of the etched graphite shows that it contains two types of primordial Xe (i.e., Q‐Xe and El Taco Xe). The isotopic heterogeneity preserved in the Bohumilitz graphite indicates that the Bohumilitz graphite did not experience any high‐temperature event and, consequently, must have been emplaced into the metal at subsolidus temperatures. This situation is incompatible with an igneous model as well as the impact melting models for the IAB‐IIICD iron meteorites as proposed by Choi et al. (1995) and Wasson et al (1980).     

The oxygen‐isotopic record in enstatite meteorites

Abstract— Oxygen‐isotopic compositions were determined for a suite of enstatite chondrites and aubrites. In agreement with previous work (Clayton et al., 1984), most samples have O‐isotopic compositions close to the terrestrial fractionation line (TFL), and there appear to be no significant differences in O‐isotopic compositions between individual EH and EL chondrites and aubrites. Five enstatite meteorites have O‐isotopic compositions that are significantly different from the other samples and >0.2% away from the TFL. Two of these have petrographic evidence of brecciation and interaction between other meteorite types; for the other three, similar scenarios are suggested. There appears to be a systematic increase in δ¹⁸O from enstatite chondrites (both EH and EL) of petrologic type 3 to those of type 6. There is also good evidence that the EH meteorites do not fall along a mass fractionation line but along a line slope 0.66. At the present time, detailed understanding of the origin of these O‐isotopic systematics remain elusive but clearly point to a complex accretion history, parent‐body evolution, or both.     

The identification of early condensates from the solar nebula

Calcium-aluminum-rich chondrules which are highly deficient in alkalis were extracted from the carbonaceous chondrite Allende and yield a range of compositions with the lowest measured isotopic composition of $\text{(}{}^{87}\text{Sr}\text{/}{}^{86}\text{Sr}\text{)}{}_{\mathrm{<mtext>ALL</mtext>}}\text{= 0.69877±0.00002}$ and identify this material as the earliest known condensate from the solar nebula. Other chondrules suggest the possible presence of even more primitive Sr in this meteorite. This result also shows that some chondritic material formed very near the earliest part of the condensation sequence. Using alkali-deficient planetary objects (Moon, basaltic achondrites, Angra dos Reis, Allende), the Sr data indicate a time interval for condensation of 10 m.y. (from ALL to BABI) if condensation occurred in a solar Rb/Sr environment. A variety of alkali-rich olivine chondrules and CaAl-rich aggregates from Allende fail to determine an isochron and indicate that the element distribution in this meteorite was disturbed later than 3.6ae, possibly recently, in a cometary nucleus. This disturbance requires that the determination of initial ⁸⁷Sr/⁸⁶Sr be done on essentially Rb-free phases. Strontium data from equilibrated chondrites and from an iron meteorite establish an interval for metamorphism or differentiation in protoplanetary objects which followed the condensation process by ≈80 mm.y. The chronology for condensation and early planetary evolution obtained for Sr is in disagreement with the ¹²⁹I chronology but can be brought into agreement, if it is assumed that the high temperature iodine containing phases have not been affected by the metamorphic events determined by Sr.     

Martian “microfossils” in lunar meteorites?

Abstract— One of the five lines of evidence used by McKay et al. (1996) for relic life in the Martian meteorite Allan Hills (ALH) 84001 was the presence of objects thought to be microfossils. These ovoid and elongated forms are similar to structures found in terrestrial rocks and described as “nanobacteria” (Folk, 1993; McBride et al, 1994). Using the same procedures and apparatus as McKay et al. (1996), we have found structures on internal fracture surfaces of lunar meteorites that cannot be distinguished from the objects described on similar surfaces in ALH 84001. The lunar surface is currently a sterile environment and probably always has been. However, the lunar and Martian meteorites share a common terrestrial history, which includes many thousands of years of exposure to Antarctic weathering. Although we do not know the origin of these ovoid and elongated forms, we suggest that their presence on lunar meteorites indicates that the objects described by McKay et al. (1996) are not of Martian biological origin.     

Magnesium isotopic fractionations in barred olivine chondrules from the Allende meteorite

Abstract— The Mg‐isotopic compositions in five barred olivine (BO) chondrules, one coarse‐grained rim of a BO chondrule, a relic spinel in a BO chondrule, one skeletal olivine chondrule similar to BO chondrules in mineralogy and composition, and two non‐BO chondrules from the Allende meteorite have been measured by thermal ionization mass spectrometry. The Mg isotopes are not fractionated and are within terrestrial standard values (±2.0%o per amu) in seven of the eight analyzed ferromagnesian chondrules. A clump of relic spinel grain and its host BO chondrule R‐11 give well‐resolvable Mg fractionations that show an enrichment of the heavier isotopes, up to +2.5%‰ per amu. The Mg‐isotopic compositions of coarse‐grained rim are identical to those of the host chondrule with BO texture. The results imply that ferromagnesian and refractory precursor components of the Allende chondrule may have been formed from isotopically heterogeneous reservoirs. In the nebula region where Allende chondrules formed, recycling of chondrules and multiple high‐temperature heating did not significantly alter the chemical and isotopic memory of earlier generations. Chemical and isotopic characteristics of refractory precursors of carbonaceous chondrite chondrules and CAIs are more closely related than previously thought. One of the refractory chondrule precursors of CV Allende is enriched in the heavier Mg isotopes and different from those of more common ferromagnesian chondrule precursors. The most probable scenario at the location where chondrule R‐11 formed is as follows. Before chondrule formation, several high‐temperature events occurred and then RPMs, refractory oxides, and silicates condensed from the nebular gas in which Mg isotopes were fractionated. Then, this CAI was transported into the chondrule formation region and mixed with more common, ferromagnesian precursors with normal Mg isotopes, and formed the BO chondrule. Because Mg isotope heterogeneity among silicates and spinel are found in some CAIs (Esat and Taylor, 1984), we cannot rule out the possibility that Mg isotopes of a melted portion of the refractory precursor (i.e., outer portion of CAI) are normal or enriched in the light isotope. Magnesium isotopes in the R‐11 host are also enriched in the heavier isotopes, +2.5%o per amu, which suggests that effects of isotopic heterogeneity among silicates and spinel, if they existed, are not considered to be large. It is possible that CAI precursor silicates partially dissolved during the chondrule forming event, contributing Mg to the melt and producing a uniform Mg‐isotopic signature but enriched in the heavier Mg isotopes, +2.5%‰ per amu. Most Mg isotopes in more common ferromagnesian chondrules represent normal chondritic material. Chemical and Mg‐isotopic signatures formed during nebular fractionations were not destroyed during thermal processes that formed the chondrule, and these were partly preserved in relic phases. Recycling of Allende chondrules and multiple heating at high temperature did not significantly alter the chemical and Mg‐isotopic memory of earlier generations.     

GROSSULAR IN THE ALLENDE (TYPE III CARBONACEOUS) METEORITE*

Grossular garnet has been observed in several white inclusions in the Allende meteorite. Compositions range from Gro_9sPy₅ to Gro₈₈Py₁₂ in five inclusions. Its mottled appearance indicates that it crystallized from a glass of near-grossular composition and not by a solid state reaction between wollastonite, anorthite and melilite. These grossular-bearing inclusions either condensed directly as metastable liquids from the solar nebula or if initial solid condensates were liquefied by some subsequent heating process. In either case, a prolonged residence time in a thermal blanket appears necessary to effect crystallization of the grossular.     

Terrestrial ages of ordinary chondrites from the Lewis Cliff stranding area,East Antarctica

Abstract— We determined terrestrial ages of ordinary chondrites from the Lewis Cliff stranding area, East Antarctica, on the basis of the concentrations of cosmogenic ¹⁰Be (t_½; = 1.51 Ma), ²⁶Al (t_½; = 0.705 Ma), and ³⁶Cl (t_½; = 0.301 Ma). After an initial ²⁶Al γ-ray survey of 91 meteorites suggested that many have terrestrial ages >0.1 Ma, we selected 62 meteorites for ¹⁰Be and ²⁶Al measurements by accelerator mass spectrometry (AMS) and measured ³⁶Cl in twelve of those. Low terrestrial ages (<0.1 Ma) were found for ～60% of the meteorites, whereas all others have ages between 0.1 and 0.5 Ma, except for one exceptional age of >2 Ma (Welten et al., 1997). Our major conclusions are: (1) The Lewis Cliff H-chondrites show similar ages to those from the Allan Hills icefields, but the L-chondrites are about a factor of 2 younger than those from Allan Hills, which indicates that Lewis Cliff is a younger stranding area. (2) The terrestrial age distributions at different parts of the Lewis Cliff stranding area generally agree with simple meteorite concentration models, although differences in weathering rate may also play a role. (3) We confirm that meteorites with natural thermoluminescence (TL) levels >80 krad are associated with low terrestrial ages (Benoit et al., 1992) but conclude that natural TL levels <80 krad can not be used to calculate the terrestrial age of a meteorite. Natural TL levels do seem useful to estimate relative terrestrial ages of large groups of meteorites and to determine differences in the surface exposure age of paired meteorite fragments. (4) Of the 62 meteorites measured with AMS, 31 were assigned to 11 different pairing groups, mainly on the basis of their cosmogenic nuclide record. The meteorites are estimated to represent between 42 and 52 distinct falls.     

RARE EARTH AND OTHER ELEMENTS IN COMPONENTS OF THE ABEE ENSTATITE CHONDRITE

Abee clast samples, a matrix sample, a dark inclusion, magnetic and nonmagnetic samples, and bulk samples were analyzed by neutron activation analysis (NAA). The REE were determined by radiochemical NAA. Na, K, Sc, Cr, Mn, Fe, Co, Ni, Zn, As, Se, Sm, Ir, Au were determined by instrumental NAA. High abundances of As, Ir, and Au in the magnetic separate and the correlation of their abundances with the metal content of the clasts indicate that As, Ir, and Au chiefly occur in the metal. Correlations for Zn and Sc indicate that they chiefly occur in niningerite, but a significant amount of Sc may also occur in oldhamite. The dark inclusions do not follow the As and Zn correlations, suggesting that the dark inclusions and clasts are not equilibrated with each other. Correlation of the REE and oldhamite abundances for both the clasts and dark inclusions indicates that the REE chiefly occur in oldhamite. In view of the INAA and mineralogical evidence for non-equilibration among the clasts and a dark inclusion (Sears et al., 1981), the similar REE patterns for clasts (3,3) and dark inclusion (5,1), and the similar mineral composition of oldhamite in clast (3,3) and dark inclusion (5,1), suggest that the oldhamite in the clasts and dark inclusions is of a common origin, which Sears et al. (1981) showed could be formed by condensation. A Tb anomaly of a factor of 2 was found in sample (2,9 and 9,2), and a La anomaly of a factor of 2 was found in clast (3,3). The only other REE anomaly in Abee, a factor of 3.5 for Yb, was found by Nakamura and Masuda(1973). In view of the evidence for equilibration among the clasts, this anomaly must have been introduced shortly before the brecciation process and indicates that no significant reheating has occurred. This concurs with the findings of Sugiura and Strangeway (1981) and Bogard et al. (1982).     

GAS RELEASE AND ORDERING OF CARBON IN THE ALLENDE METEORITE

Mass-spectrometric determinations of the inert gas release from samples of the Allende carbonaceous meteorite heated in the range 300°C to 1100°C, followed by Raman spectroscopic studies of the 1360 cm^?1 and 1580 cm^?1 bands of carbon support the hypothesis that the gas release at high temperatures is causally related with ordering of carbon.     

Refractory forsterite in primitive meteorites: Condensates from the solar nebula?

Abstract— All groups of chondritic meteorites contain discrete grains of forsteritic olivine with FeO contents below 1 wt% and high concentrations of refractory elements such as Ca, Al, and Ti. Ten such grains (52 to 754 μg) with minor amounts of adhering matrix were separated from the Allende meteorite. After bulk chemical analysis by instrumental neutron activation analysis (INAA), some samples were analyzed with an electron microprobe and some with an ion microprobe. Matrix that accreted to the forsterite grains has a well‐defined unique composition, different from average Allende matrix in having higher Cr and lower Ni and Co contents, which implies limited mixing of Allende matrix. All samples have approximately chondritic relative abundances of refractory elements Ca, Al, Sc, and rare‐earth elements (REE), although some of these elements, such as Al, do not quantitatively reside in forsterite; whereas others (e.g., Ca) are intrinsic to forsterite. The chondritic refractory element ratios in bulk samples, the generally high abundance level of refractory elements, and the presence of Ca‐Al‐Ti‐rich glass inclusions suggest a genetic relationship of refractory condensates with forsteritic olivine. The Ca‐Al‐Ti‐rich glasses may have acted as nuclei for forsterite condensation. Arguments are presented that exclude an origin of refractory forsterite by crystallization from melts with compositions characteristic of Allende chondrules: (a) All forsterite grains have CaO contents between 0.5 and 0.7 wt% with no apparent zoning, requiring voluminous parental melts with 18 to 20 wt% CaO, far above the average CaO content of Allende chondrules. Similar arguments apply to Al contents. (b) The low FeO content of refractory forsterite of 0.2‐0.4 wt% imposes an upper limit of ～1 wt% of FeO on the parental melt, too low for ordinary and carbonaceous chondrule melts, (c) The Mn contents of refractory forsterites are between 30 to 40 ppm. This is at least one order of magnitude below the Mn content of chondrule olivines in all classes of meteorites. The observed Mn contents of refractory forsterite are much too low for equilibrium between olivine and melts of chondrule composition, (d) As shown earlier, refractory forsterites have O‐isotopic compositions different from chondrules (Weinbruch et al., 1993a). Refractory olivines in carbonaceous chondrites are found in matrix and in chondrules. The compositional similarity of both types was taken to indicate that all refractory forsterites formed inside chondrules (e.g., Jones, 1992). As refractory forsterite cannot have formed by crystallization from chondrule melts, we conclude that refractory forsterite from chondrules are relic grains that survived chondrule melting and probably formed in the same way as refractory forsterite enclosed in matrix. We favor an origin of refractory forsterite by condensation from an oxidized nebular gas.