D. J. Schlutter

Isotopic Compositions of Cometary Matter Returned by Stardust

Hydrogen, carbon, nitrogen, and oxygen isotopic compositions are heterogeneous among comet 81P/Wild 2 particle fragments; however, extreme isotopic anomalies are rare, indicating that the comet is not a pristine aggregate of presolar materials. Nonterrestrial nitrogen and neon isotope ratios suggest that indigenous organic matter and highly volatile materials were successfully collected. Except for a single 17O-enriched circumstellar stardust grain, silicate and oxide minerals have oxygen isotopic compositions consistent with solar system origin. One refractory grain is 16O-enriched, like refractory inclusions in meteorites, suggesting that Wild 2 contains material formed at high temperature in the inner solar system and transported to the Kuiper belt before comet accretion.

An asteroidal breccia: The anatomy of a cluster IDP

Abstract We report results of a consortium study of a large interplanetary dust particle known as cluster L2008#5. This cluster is composed of fifty-three fragments (>5 pm in diameter) and several hundred fines ( Several methods were used to estimate the degree of heating that this cluster experienced. Variations in the inferred peak temperatures experienced by different fragments suggest that a thermal gradient was maintained. The cluster as a whole was not strongly heated; it is estimated to have a low earth-encounter velocity which is consistent with origin from an object in an asteroidal orbit rather than from a comet, which would most likely have a high entry velocity. Our conclusions show that cluster L2008#5 consists of a chemically and mineralogically diverse mixture of fragments. We believe that cluster L2008#5 represents a heterogeneous breccia and that it was most likely derived from an object in an asteroidal orbit. We also present an important cautionary note for attempts to interpret individual, small-sized 10–15 μm IDPs as representative of parent bodies. It is not unique that individual building blocks of IDPs, such as discrete olivine, pyroxene, sulfide grains, regions of carbonaceous material, and other noncrystalline material, are found in several fragments; however, it is unique that these building blocks are combined in various proportions in related IDPs from one large cluster particle.

Irradiation records in regolith materials. I: isotopic compositions of solar-wind neon and argon in single lunar mineral grains

Abstract We have applied a stepwise pyrolytic extraction technique to eleven individual lunar regolith grains to investigate the compositions of light noble gases embedded in grain surfaces by solar wind irradiation, with emphasis on the rather poorly known isotopic composition of solar-wind argon. Results are intriguing: average 20 Ne/ 22 Ne ratios observed in early pyrolytic releases from ilmenite grains separated from lunar soils 71501, 79035 and 10084 agree very well with both direct measures of the solar wind neon composition in the Apollo foils and with values obtained in first releases from acid-etched ilmenites by the Zurich laboratory, whereas these same pyrolytic and acid-etch fractions carry argon isotopic signatures that significantly disagree—average 36 Ar/ 38 Ar ratios near 5.8 for thermal extraction compared to 5.4–5.5 for chemical etching at Zurich. Consideration of the isotopic and elemental data from these grains in the context of first-order diffusive modeling calculations points to gas release at low temperatures, without significant isotopic or elemental fractionation, from isolated grain-surface reservoirs of solar wind composition. The physical nature of these reservoirs is presently unknown. In this interpretation the preferred solar wind 20 Ne/ 22 Ne and 21 Ne/ 22 Ne ratios deduced from this study are respectively 13.81 ± 0.08 and 0.0333 ± 0.0003, both within error of the Zurich acid-etch values, and 36 Ar/ 38 Ar = 5.77 ± 0.08. It may be possible to reconcile the discrepancy between the acid-etch and pyrolytic estimates for the solar wind 36 Ar/ 38 Ar ratio in the context of arguments originally advanced by Benkert et al. (1993) to account for their He and Ne isotopic compositions. At the other, high-temperature end of the release profile from one of these grains there are clear isotopic indications of the presence of a Ne constituent with 20 Ne/ 22 Ne close to the 11.2 ratio found at Zurich and attributed by these workers to a deeply-sited component implanted by solar energetic particles.

The Genesis solar-wind collector materials

Genesis (NASA Discovery Mission #5) is a sample return mission. Collectors comprised of ultra-high purity materials will be exposed to the solar wind and then returned to Earth for laboratory analysis. There is a suite of fifteen types of ultra-pure materials distributed among several locations. Most of the materials are mounted on deployable panels (‘collector arrays’), with some as targets in the focal spot of an electrostatic mirror (the ‘concentrator’). Other materials are strategically placed on the spacecraft as additional targets of opportunity to maximize the area for solar-wind collection.Most of the collection area consists of hexagonal collectors in the arrays; approximately half are silicon, the rest are for solar-wind components not retained and/or not easily measured in silicon. There are a variety of materials both in collector arrays and elsewhere targeted for the analyses of specific solar-wind components.Engineering and science factors drove the selection process. Engineering required testing of physical properties such as the ability to withstand shaking on launch and thermal cycling during deployment. Science constraints included bulk purity, surface and interface cleanliness, retentiveness with respect to individual solar-wind components, and availability.A detailed report of material parameters planned as a resource for choosing materials for study will be published on a Genesis website, and will be updated as additional information is obtained. Some material is already linked to the Genesis plasma data website (genesis.lanl.gov). Genesis should provide a reservoir of materials for allocation to the scientific community throughout the 21st Century.

Helium and neon isotopes in deep Pacific Ocean sediments

Helium and neon concentration measurements, along with isotope ratio determinations, have been made for particles collected in the deep Pacific with a magnetic sled, and they are believed to be of extraterrestrial origin. Analyses were made for samples consisting of composites of many extremely fine particles and for several individual particles large enough to contain sufficient gas for analysis but small enough to escape melting in their passage through the atmosphere. Step-heating was employed to extract the gas. Cosmic-ray spallation products or solar-wind helium and neon, if present, were not abundant enough to account for the isotopic compositions measured. In the case of the samples of magnetic fines, the low temperature extractions provided elemental and isotopic ratios in the general range found for the primordial gas in carbonaceous chondrites and gas-rich meteorites. The isotopic ratios found in the high temperature extractions suggest the presence of solar-flare helium and neon.

Irradiation records in regolith materials, II: Solar wind and solar energetic particle components in helium, neon, and argon extracted from single lunar mineral grains and from the Kapoeta howardite by stepwise pulse heating

Abstract High-resolution stepped heating has been used to extract light noble gases implanted in a suite of 13 individual lunar ilmenite and iron grains and in the Kapoeta howardite by solar wind (SW) and solar energetic particle (SEP) irradiation. Isotopic analyses of gases evolved at low temperatures from the lunar grains confirm the neon and argon compositions obtained by Pepin et al. (Pepin R. O., Becker R. H., and Schlutter D. J., “Irradiation records in regolith materials, I: Isotopic compositions of solar-wind neon and argon in single lunar regolith grains”, Geochim. Cosmochim. Acta63, 2145–2162, 1999) in an initial study of 11 regolith grains, primarily ilmenites. Combination of the data sets from both investigations yields 20Ne/22Ne = 13.85 ± 0.04, 21Ne/22Ne = 0.0334 ± 0.0003, and 36Ar/38Ar = 5.80 ± 0.06 for the lunar samples; the corresponding 36Ar/38Ar ratio in Kapoeta is 5.74 ± 0.06. The neon ratios agree well with those measured by Benkert et al. (Benkert J.-P., Baur H., Signer P., and Wieler R., “He, Ne, and Ar from the solar wind and solar energetic particles in lunar ilmenites and pyroxenes”, J. Geophys. Res. (Planets) 98, 13147–13162, 1993) in gases extracted from bulk lunar ilmenite samples by stepped acid etching and attributed by them to the SW. The 36Ar/38Ar ratios, however, are significantly above both Benkert et al.’s (1993) proposed SW value of 5.48 ± 0.05 and a later estimate of 5.58 ± 0.03 from an acid-etch analysis of Kapoeta (Becker R. H., Schlutter D. J., Rider P. E., and Pepin R. O., “An acid-etch study of the Kapoeta achondrite: Implications for the argon-36/argon-38 ratio in the solar wind”, Meteorit. Planet. Sci. 33, 109–113, 1998). We believe, for reasons discussed here and in our earlier report, that 5.80 ± 0.06 ratio most nearly represents the wind composition. The 3He/4He ratio in low-temperature gas releases, not measured in the first particle suite, is found in several grains to be indistinguishable from Benkert et al.’s (1993) SW estimate. Elemental ratios of He, Ne, and Ar initially released from grain-surface SW implantation zones are solar-like, as found earlier by Pepin et al. (1999). Gases evolved from these reservoirs at higher temperatures show evidence for perturbations from solar elemental compositions by prior He loss, thermal mobilization of excess Ne from fractionated SW components, or both. Attention in this second investigation was focused on estimating the isotopic compositions of both the SW and the more deeply sited SEP components in regolith grains. Several high-temperature “isotopic plateaus”—approximately constant isotopic ratios in gas fractions released over a number of consecutive heating steps—were observed in the close vicinities of the SEP ratios for He, Ne, and Ar reported by Benkert et al. (1993). Arguments presented in the text suggest that these plateaus are relatively free of interferences from multicomponent mixing artifacts that can mimic pure component signatures. Average SEP compositions derived from the stepped-heating plateau measurements are in remarkable agreement with the Zurich acid-etch values for all three gases.

Helium and Neon Abundances and Compositions in Cometary Matter

Materials trapped and preserved in comets date from the earliest history of the solar system. Particles captured by the Stardust spacecraft from comet 81P/Wild 2 are indisputable cometary matter available for laboratory study. Here we report measurements of noble gases in Stardust material. Neon isotope ratios are within the range observed in “phase Q,” a ubiquitous, primitive organic carrier of noble gases in meteorites. Helium displays 3He/4He ratios twice those in phase Q and in Jupiters atmosphere. Abundances per gram are surprisingly large, suggesting implantation by ion irradiation. The gases are probably carried in high-temperature igneous grains similar to particles found in other Stardust studies. Collectively, the evidence points to gas acquisition in a hot, high ion-flux nebular environment close to the young Sun.

3He/4He in Stardust Samples

ICP and XRF Spectroscopy methods were used to evaluate the metals (ppm) from soils for the mining dumps of Crucea- Botusana uranium deposit (Bistrita Mountains, Romania). The sequential extraction has emphasized the fact that U is associated with all the mineral fractions present in the soil samples. A great percentage of U can be found in the carbonate, organic and oxides fractions. The percentage of U detected in the exchangeable fraction is rather small. The fact that 21.77% of the total U can be found in the specifically absorbed and carbonate bound fraction, indicated the important role played by the carbonates in the retention of U; one the other hand this fraction is liable to release U if the pH should happen to change.Th appear in high-enough concentration in the soil is scarcely available because 70.29% is present in residual fraction, and about 21.78% in the organic and oxides fractions. This is certainly due to the fact that this naturally occurring radionuclide can be associated with relatively insoluble mineral phases like alumino-silicates and refractory oxides. Its association with the organic matter suggests that it can form soluble organic complexes that can facilitate its removal by the stream waters. In the case of Sr, the sequential extraction shows that it is very strongly fixed because the residual fraction concentrates the great amount of this element. What is interesting is the percentage of 2.65 % of Sr from the exchangeable fraction because it can be easily released and transported to the surrounding environment. Pb it is present in various relatively soluble pools (17.81% in carbonate boud and 34.85% in organically bound), which appears to be an efficient sink for this element. This fact may indicate a possible link between the biological activity and the Pb cycling into the soil. In addition, only 17.78% is present in the insoluble residual fraction. Although from our research it resulted that the radioactive metals does not concentrate in the exchangeable fraction (Th) or it concentrates very little in it (U and Sr), the isolation of the mineral fraction of soil rich in U, Th and Sr helps us in the future identification of the connections which control the cycle of the radioactive metals. These results have important implications for remediation strategies. The thorium and uranium from Crucea mining area are in labile, not strongly retained, fractions, thus making them amendable for remediation by phytoremediation.