John M. Allen

Two forsterite-bearing FUN inclusions in the Allende meteorite

We have discovered two FUN inclusions, CG-14 and TE, among a group of five forsterite-rich inclusions in Allende, two of which are described for the first time herein. All five consist of euhedral forsterite and spinel crystals poikilitically enclosed by fassaite. Forsterite and spinel are usually segregated from one another, sometimes into a spinel-rich mantle and a forsterite-rich core. Some inclusions contain vesicles, indicating that they were once molten. The crystallization sequence inferred from textures is: spinel, forsterite, fassaite and, finally, Mg-rich melilite. One concentrically-zoned inclusion contains melilite in its mantle whose composition lies on the opposite side of the liquidus minimum in the melilite binary from that in its core. This suggests that segregation of forsterite from spinel in all of these inclusions could be due to volatilization of MgO and SiO2 relative to Al2O3 and CaO from the outsides of droplets. CG-14 is relatively uniformly enriched in refractory elements relative to Cl chondrites by a factor similar to that for Ca-, Al-rich coarse-grained inclusions except for Ca, Al and Hf which are unusually low. No Ce anomaly such as found in FUN inclusions Cl and HAL is present in CG-14. Whole-rock samples of CG-14 and TE are more strongly mass-fractionated in oxygen relative to “normal” Allende inclusions than the FUN inclusion EK 1-4-1 and less so than Cl. Relative to bulk Allende, both inclusions have strongly massfractionated magnesium and silicon and 25Mg excesses or deficits of 24Mg or 26Mg. CG-14 has a 29Si excess or a deficit of 28Si or 30Si. Volatilization loss cannot be responsible for the magnesium and silicon isotope fractionations, as this would require prohibitively large mass loss from these magnesium-rich inclusions. The remarkable similarity in textures between FUN and non-FUN inclusions implies similar thermal histories, arguing against different rates of evaporative loss of major elements. Sputtering alone may be insufficient to account for the magnitude and direction of oxygen isotope fractionation in FUN inclusions.

Mineralogy and petrography of HAL, an isotopically-unusual Allende inclusion

A detailed mineralogical study of HAL was initiated to elucidate the origin of this inclusion because LEE et al. (1979) had found large mass fractionation effects and small nuclear effects in its Ca isotopic composition, but no ^(26)Mg excesses in samples of it with very high ^(27)Al/^(24)Mg ratios. HALs 1.0 mm radius interior consists almost entirely of three hibonite crystals and is surrounded by a 2.0 mm thick, multi-layered rim. The first layer, called the black rim, is black and compact, resembles a devitrified glass and contains an anisotropic Al-Fe-oxide similar to hercynite in composition. This is followed by a friable rim sequence, layer I of which is predominantly feldspathoids with minor anorthite, Ti-Fe-oxide and Al-Fe-oxide. Layer II contains abundant perovskite, plus grossular, andradite and pyroxene in addition to the minerals of layer I. Layer III is mostly Ca-phosphate, possibly hydroxy-apatite and perovskite. Layer IV is rich in hibonite, Al-Fe-oxide, perovskite, nepheline and the two garnets, lacks Ca-phosphate but contains traces of a Ti-Sc-Zr-oxide. Layer V is rich in Al-Fe-oxide, pyroxene, nepheline, the two garnets and olivine whose crystals display peculiar rectangular cross-sections. The black rim does not completely surround the hibonite core. Sectors of the friable rim exist where layer I is missing and where the mineralogy of adjacent layers is no different from that of the same layers in other sectors. Pentlandite, nickel-iron and barrel-shaped olivine crystals, minerals typical of the matrix of Allende and found nowhere else in HAL, are found in layer V and increase in abundance toward its exterior, as if grains of these phases accreted together with the other minerals of layer V. This layer also contains alternating olivine-rich and garnet-, pyroxene-rich bands, resembling rhythmic layering. For these reasons, we conclude that each of the layers of the friable rim formed by the accretion of an assemblage of condensate grains rather than by complete reaction of a precursor to HAL with a nebular gas. Thus, the unusual isotopic characteristics of HAL are thought to have been inherited from a nebular reservoir which was isotopically distinct from that which gave rise to the bulk of the material in Allende. HALs mineralogical peculiarities indicate that its formation reservoir was also chemically distinct from the latter one.

Electron microprobe study of a ‘mysterite’-bearing inclusion from the Krymka LL-chondrite

The black inclusion from the Krymka LL3 chondrite previously found to contain ‘mysterite’ by Lewiset al. (1979) belongs to a hitherto unknown class of carbonaceous chondrites. Its olivine and pyroxene compositions. Fo 97–99 and En 96, respectively, are characteristic of carbonaceous chondrites and its plagioclase composition. An 100, is characteristic of C3s. It contains a peculiar group of Co-, Cr-rich metal grains whose compositions are similar, but not identical, to those in C2 chondrites and which also bear some similarities to those in Renazzo. Its weight ratios of total FeSiO2 and solSiO2MgO are 0.74 and 1.43, respectively, and its atomic ratio of SiAl is 10.7, exactly the same as in carbonaceous chondrites. Its bulk chemical composition is very close to that of the Murchison C2 chondrite. The association of mysterite with a special type of carbonaceous chondrite material suggests that mysterite formed by low-temperature condensation in a different region of the nebula from other carbonaceous chondrites.