ABSTRACT
The solar system formed from interstellar dust and gas in a molecular cloud. Astronomical observations show that typical interstellar dust consists of amorphous (a-) silicate and organic carbon. Bona fide physical samples for laboratory studies would yield unprecedented insight about solar system formation, but they were largely destroyed. The most likely repositories of surviving presolar dust are the least altered extraterrestrial materials, interplanetary dust particles (IDPs) with probable cometary origins. Cometary IDPs contain abundant submicron a-silicate grains called GEMS (glass with embedded metal and sulfides), believed to be carbon-free. Some have detectable isotopically anomalous a-silicate components from other stars, proving they are preserved dust inherited from the interstellar medium. However, it is debated whether the majority of GEMS predate the solar system or formed in the solar nebula by condensation of high-temperature (>1,300 K) gas. Here, we map IDP compositions with single nanometer-scale resolution and find that GEMS contain organic carbon. Mapping reveals two generations of grain aggregation, the key process in growth from dust grains to planetesimals, mediated by carbon. GEMS grains, some with a-silicate subgrains mantled by organic carbon, comprise the earliest generation of aggregates. These aggregates (and other grains) are encapsulated in lower-density organic carbon matrix, indicating a second generation of aggregation. Since this organic carbon thermally decomposes above â¼450 K, GEMS cannot have accreted in the hot solar nebula, and formed, instead, in the cold presolar molecular cloud and/or outer protoplanetary disk. We suggest that GEMS are consistent with surviving interstellar dust, condensed in situ, and cycled through multiple molecular clouds.
ABSTRACT
Filamentary enstatite crystals are found in interplanetary dust particles (IDPs) of likely cometary origin but are very rare or absent in meteorites. Crystallographic characteristics of filamentary enstatites indicate that they condensed directly from vapor. We measured the O isotopic composition of an enstatite ribbon from a giant cluster IDP to be δ18O = 25 ± 55, δ17O = -19 ± 129, Δ17O = -32 ± 134 (2σ errors), which is inconsistent at the 2σ level with the composition of the Sun inferred from the Genesis solar wind measurements. The particle's O isotopic composition, consistent with the terrestrial composition, implies that it condensed from a gas of nonsolar O isotopic composition, possibly as a result of vaporization of disk region enriched in 16O-depleted solids. The relative scarcity of filamentary enstatite in asteroids compared to comets implies either that this crystal condensed from dust vaporized in situ in the outer solar system where comets formed or it condensed in the inner solar system and was subsequently transported outward to the comet-forming region.
ABSTRACT
Magnesium stable isotope ratios and minor element abundances of five olivine particles from comet 81P/Wild 2 were examined by secondary ion mass spectrometry (SIMS). Wild 2 olivine particles exhibit only small variations in δ25Mg values from -1.0 +0.4/-0.5 to 0.6 +0.5/- 0.6 (2σ). This variation can be simply explained by mass-dependent fractionation from Mg isotopic compositions of the Earth and bulk meteorites, suggesting that Wild 2 olivine particles formed in the chondritic reservoir with respect to Mg isotope compositions. We also determined minor element abundances, and O and Mg isotope ratios of olivine grains in amoeboid olivine aggregates (AOAs) from Kaba (CV3.1) and DOM 08006 (CO3.01) carbonaceous chondrites. Our new SIMS minor element data reveal uniform, low FeO contents of ~0.05 wt% among AOA olivines from DOM 08006, suggesting that AOAs formed at more reducing environments in the solar nebula than previously thought. Furthermore, the SIMS-derived FeO contents of the AOA olivines are consistently lower than those obtained by electron microprobe analyses (~1 wt% FeO), indicating possible fluorescence from surrounding matrix materials and/or Fe,Ni-metals in AOAs during electron microprobe analyses. For Mg isotopes, AOA olivines show more negative mass-dependent fractionation (-3.8 ± 0.5 ≤ δ25Mg ≤ -0.2 ± 0.3; 2σ) relative to Wild 2 olivines. Further, these Mg isotope variations are correlated with their host AOA textures. Large negative Mg isotope fractionations in olivine are often observed in pore-rich AOAs, while those in compact AOAs tend to have near-chondritic Mg isotopic compositions. These observations indicate that pore-rich AOAs preserved their gas-solid condensation histories, while compact AOAs experienced thermal processing in the solar nebula after their condensation and aggregation. Importantly, one 16O-rich Wild 2 LIME olivine particle (T77/F50) shows negative Mg isotope fractionation (δ25Mg = -0.8 ± 0.4, δ26Mg = -1.4 ± 0.9; 2σ) relative to bulk chondrites. Minor element abundances of T77/F50 are in excellent agreement with those of olivines from pore-rich AOAs in DOM 08006. The observed similarity in O and Mg isotopes, and minor element abundances suggest that T77/F50 formed in an environment similar to AOAs, probably near the proto-Sun, and then was transported to the Kuiper belt, where comet 81P/Wild 2 likely accreted.
ABSTRACT
In order to explore the link between comet 81P/Wild 2 and materials in primitive meteorites, seven particles 5 to 15 µm in diameter from comet 81P/Wild 2 have been analyzed for their oxygen isotope ratios using a secondary ion mass spectrometer. Most particles are single minerals consisting of olivine or pyroxene with Mg# higher than 85, which are relatively minor in 81P/Wild 2 particles (~1/3 of the 16O-poor cluster). Four particles extracted from Track 149 are 16O-poor and show Δ17O (= δ17O - 0.52 × Î´18O) values from -2%0 to +1%0, similar to previous studies, while one enstatite (En99) particle shows lower Δ17O value of -7±4%o (2σ). This compositional range has not been reported among 16O-poor particles in 81P/Wild 2, but is commonly observed among chondrules in carbonaceous chondrites and in particular in CR chondrites. The distribution in Δ17O indicates that 16O-poor 81P/Wild 2 particles are most similar to chondrules (and their fragments) in the CR chondrites and Tagish Lake-like WIS91600 chondrite chondrule silicate grains, which indicates that they likely come from a reservoir with similar dust/ice ratios as CR chondrites and WIS91600. However, differences in the Mg# distribution imply that the 81P/Wild 2 reservoir was comparatively more oxidized, with a higher dust enrichment. Two nearly pure enstatite grains from track 172 are significantly enriched in 16O, with δ18O values of -51.2 ± 1.5%0 (2σ) and -43.0 ± 1.3% (2σ), respectively, and Δ17O values of -22.3 ± 1.9% (2σ) and -21.3 ± 2.3%0 (2σ), respectively. They are the first 16O-rich pyroxenes found among 81P/Wild 2 particles, with similar Δ17O values to those of 16O-rich low-iron, manganese-enriched (LIME) olivine and CAI (calcium and aluminum-rich inclusions) -like particles from 81P/Wild 2. The major element and oxygen isotopic compositions of the pyroxenes are similar to those of enstatite in amoeboid olivine aggregates (AOAs) in primitive chondrites, in which 16O-rich pyroxenes have previously been found, and thus suggest a condensation origin.