Diffusive Mass Transport in Agglomerated Glassy Fallout from a Near-Surface Nuclear Test

1David G. Weisz, 1Benjamin Jacobsen, 1Naomi E. Marks, 1Kim B. Knight, 1Brett H. Isselhardt, 1Jennifer E. Matzel
Geochimica et Cosmochimica Acta (in Press) link to Article [https://doi.org/10.1016/j.gca.2017.12.011]
1Glenn T. Seaborg Institute, Lawrence Livermore National Laboratory, 7000 East Avenue, Livermore, CA 94550, USA
Copyright Elsevier

Aerodynamically-shaped glassy fallout is formed when vapor phase constituents from the nuclear device are incorporated into molten carriers (i.e. fallout precursor materials derived from soil or other near-field environmental debris). The effects of speciation and diffusive transport of condensing constituents are not well defined in models of fallout formation. Previously we reported observations of diffuse micrometer scale layers enriched in Na, Fe, Ca, and 235U, and depleted in Al and Ti, at the interfaces of agglomerated fallout objects. Here, we derive the timescales of uranium mass transport in such fallout as it cools from 2500 K to 1500 K by applying a 1-dimensional planar diffusion model to the observed 235U/30Si variation at the interfaces. By modeling the thermal transport between the fireball and the carrier materials, the time of mass transport is calculated to be <0.6 seconds, <1 second, <2 seconds, and <3.5 seconds for fireball yields of 0.1 kt, 1 kt, 10 kt, and 100 kt respectively. Based on the calculated times of mass transport, a maximum temperature of deposition of uranium onto the carrier material of ∼2200 K is inferred (1σ uncertainty of ∼200 K). We also determine that the occurrence of micrometer scale layers of material enriched in relatively volatile Na-species as well as more refractory Ca-species provides evidence for an oxygen-rich fireball based on the vapor pressure of the two species under oxidizing conditions. These results represent the first application of diffusion-based modeling to derive material transport, thermal environments, and oxidation-speciation in near-surface nuclear detonation environments.

Evolution of interstellar organic compounds under asteroidal hydrothermal conditions

1V. Vinogradoff, 1S. Bernard, 2C. Le Guillou, 1L. Remusata
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2017.12.019]
1Institut de Minéralogie, Physique des Matériaux et Cosmochimie, IMPMC, Sorbonne Universités, CNRS UMR 7590, Muséum National d’Histoire naturelle, MNHN, UPMC, IRD UMR 206, Paris, France
2Unité Matériaux et Transformations, UMET, UMR CNRS 8207, Université Lille 1, France
Copyright Elsevier

Carbonaceous chondrites (CC) contain a diversity of organic compounds. No definitive evidence for a genetic relationship between these complex organic molecules and the simple organic molecules detected in the interstellar medium (ISM) has yet been reported. One of the many difficulties arises from the transformations of organic compounds during accretion and hydrothermal alteration on asteroids. Here, we report results of hydrothermal alteration experiments conducted on a common constituent of interstellar ice analogs, Hexamethylenetetramine (HMT – C6H12N4). We submitted HMT to asteroidal hydrothermal conditions at 150°C, for various durations (up to 31 days) and under alkaline pH. Organic products were characterized by gas chromatography mass spectrometry, infrared spectroscopy and synchrotron-based X-ray absorption near edge structure spectroscopy. Results show that, within a few days, HMT has evolved into (1) a very diverse suite of soluble compounds dominated by N-bearing aromatic compounds (> 150 species after 31 days), including for instance formamide, pyridine, pyrrole and their polymers (2) an aromatic and N-rich insoluble material that forms after only 7 days of experiment and then remains stable through time. The reaction pathways leading to the soluble compounds likely include HMT dissociation, formose and Maillard-type reactions, e.g. reactions of sugar derivatives with amines. The present study demonstrates that, if interstellar organic compounds such as HMT had been accreted by chondrite parent bodies, they would have undergone chemical transformations during hydrothermal alteration, potentially leading to the formation of high molecular weight insoluble organic molecules. Some of the diversity of soluble and insoluble organic compounds found in CC may thus result from asteroidal hydrothermal alteration.

The Mukundpura meteorite, a new fall of CM chondrite

1Dwijesh Ray, 1Anil D.Shukla
Planetary and Space (in Press) Link to Article [https://doi.org/10.1016/j.pss.2017.11.005]
1Physical Research Laboratory, Ahmedabad 380 009, India
Copyright Elsevier

Mukundpura is a new CM chondrite fell near Jaipur, Rajasthan, India on June 6, 2017 at 5:15 IST. The fall was observed by local villager. According to eyewitness, the meteorite was fragmented into several pieces once the object hit the ground. Based on petrography, mineralogy and bulk composition, Mukundpura is classified as CM2 chondrite. The chondrules are mainly similar to type I (Olivine: Fo99). Olivines are often found associated with pyroxene (Wo10-35En62-87Fs2-7) phenocryst. However, occurrences of forsteritic and fayalitic olivine (Fa58-71) as isolated mineral clast in matrix are not uncommon. Other types of chondrules include porphyritic pyroxene (En86Fs14) and barred olivine (Fa32.7±0.3) clast. Chondrules are commonly rimmed by fine-grained accretionary dust mantles. Phyllosilicates are the most dominant secondary mineral in matrix and largely associated with poorly characterised phases (PCP). FeO/SiO2 and S/SiO2 of PCP are 2.7 and 0.4 respectively. Other phases in matrix generally include calcite (pure CaCO3), Fe-Ni metal and sulphides. Spinel and perovskite occur occasionally as inclusions. The spherical or elliptical shaped metals (within chondrule or in isolated grains) are low-Ni type (kamacite <7.5 wt%) and resembles the solar Ni/Co ratio. However, Ni content in metal rarely exceeds 8.5 wt% (up to 23 wt%, taenite). Pyrrhotite (Fe ∼62 wt%; S ∼38 wt%) and pentlandite (Fe ∼31–33 wt%, Ni ∼28–32 wt%, S ∼33 wt%)) are the common sulphides occur as isolated grains within the matrix, however, the former is the most dominant. The bulk chemical composition of Mukundpura is largely similar to other CM type chondrite (e.g. Paris CM). Based on petrography, we infer a modest aqueous alteration stage for Mukundpura while the effect of thermal metamorphism was negligible.

Structure analysis and conditions of formation of akimotoite in the Tenham chondrite

1O.Tschauner,2C. Ma,3,4C. Prescher,3V. B. Prakapenka
Meteoritics&Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.13009]
1Department of Geoscience, University of Nevada, Las Vegas, Nevada, USA
2Division of Geology and Planetary Sciences, California Institute of Technology, Pasadena, California, USA
3Center for Advanced Radiation Sources, University of Chicago, Chicago, Illinois, USA
4Institut für Geologie und Mineralogie, Universität zu Köln, Köln, Germany
Published by arrangement with John Wiley & Sons

Akimotoite (Mg,Fe)SiO3 is one of the most common mineralogical indicators for high-level shock metamorphism in meteorites. First described 1997, its occurrence has been amply confirmed in a number of highly shocked chondrites. Yet, a thorough structure analysis of natural akimotoite has remained extant. Here we report accurate cell parameters, fractional atomic coordinates, and site occupancies for natural akimotoite from the holotype specimen based on synchrotron microdiffraction. The variation of unit cell shape and volume with Fe content define mixing volumes. Based on the mixing volume relation for akimotoite and hemleyite, we constrain the unit cell volume of endmember hemleyite to 273.8 ± 1.0 Å3. We show that mixing is nearly ideal for low Fe content but evolves to positive excess volume toward the Fe endmember. Based on this finding and the actual composition of akimotoite in Tenham, we show that this mineral has formed by solid–solid transformation prograde from enstatite, not by crystallization from melt.

The Chelyabinsk meteorite: Thermal history and variable shock effects recorded by the 40Ar-39Ar system

1,2Mario Trieloff,1,2,3Ekaterina V. Korochantseva,1,2,3Alexei I. Buikin,1,2Jens Hopp,3Marina A. Ivanova,3Alexander V. Korochantsev
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.13012]
1Institut für Geowissenschaften, Universität Heidelberg, Heidelberg, Germany
2Klaus-Tschira-Labor für Kosmochemie, Universität Heidelberg, Heidelberg, Germany
3Vernadsky Institute of Geochemistry, Moscow, Russia
Published by arrangement with John Wiley & Sons

We studied three lithologies (light and dark chondritic and impact melt rock) differing in shock stage from the LL5 chondrite Chelyabinsk. Using the 40Ar-39Ar dating technique, we identified low- and high-temperature reservoirs within all samples, ascribed to K-bearing oligoclase feldspar and shock-induced jadeite–feldspar glass assemblages in melt veins, respectively. Trapped argon components had variable 40Ar/36Ar ratios even within low- and high-temperature reservoirs of individual samples. Correcting for trapped argon revealed a lithology-specific response of the K-Ar system to shock metamorphism, thereby defining two distinct impact events affecting the Chelyabinsk parent asteroid (1) an intense impact event ~1.7 ± 0.1 Ga ago formed the light–dark-structured and impact-veined Chelyabinsk breccia. Such a one-stage breccia formation is consistent with petrological observations and was recorded by the strongly shocked lithologies (dark and impact melt) where a significant fraction of oligoclase feldspar was transformed into jadeite and feldspathic glass; and (2) a young reset event ~30 Ma ago particularly affected the light lithology due to its low argon retentivity, while the more retentive shock-induced phases were more resistant against thermal reset. Trapped argon with 40Ar/36Ar ratios up to 1900 was likely incorporated during impact-induced events on the parent body, and mixed with terrestrial atmospheric argon contamination. Had it not been identified via isochrons based on high-resolution argon extraction, several geochronologically meaningless ages would have been deduced.

Search for sulfates on the surface of Ceres

1C. Bu,1G. Rodriguez Lopez,1C. A. Dukes,2O. Ruesch,2L. A. McFadden,3J.-Y. Li
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.13024]
1Laboratory for Astrophysics and Surface Physics, University of Virginia, Charlottesville, Virginia, USA
2NASA Goddard Space Flight Center, Greenbelt, Maryland, USA
3Planetary Science Institute, Tucson, Arizona, USA
Published by arrangement with John Wiley & Sons

The formation of hydrated salts is an expected consequence of aqueous alteration of Main Belt objects, particularly for large, volatile-rich protoplanets like Ceres. Sulfates, present on water-bearing planetary bodies (e.g., Earth, Mars, and carbonaceous chondrite parent bodies) across the inner solar system, may contribute to Ceres’ UV and IR spectral signature along with phyllosilicates and carbonates. We investigate the presence and stability of hydrated sulfates under Ceres’ cryogenic, low-pressure environment and the consequent spectral effects, using UV–Vis–IR reflectance spectroscopy. H2O loss begins instantaneously with vacuum exposure, measured by the attenuation of spectral water absorption bands, and a phase transition from crystalline to amorphous is observed for MgSO4·6H2O by X-ray powder diffraction. Long-term (>40 h), continuous exposure of MgSO4·nH2O (n = 0, 6, 7) to low pressure (10−3–10−6 Torr) causes material decomposition and strong UV absorption below 0.5 μm. Our measurements suggest that MgSO4·6H2O grains (45–83 μm) dehydrate to 2% of the original 1.9 μm water band area over ~0.3 Ma at 200 K on Ceres and after ~42 Ma for 147 K. These rates, inferred from an Avrami dehydration model, preclude MgSO4·6H2O as a component of Ceres’ surface, although anhydrous and minimally hydrated sulfates may be present. A comparison between Ceres emissivity spectra and laboratory reflectance measurements over the infrared range (5–17 μm) suggests sulfates cannot be excluded from Ceres’ mineralogy.

Theoretical analysis of the atmospheric entry of sub-mm meteoroids of MgxCa1−xCO3 composition

1G. Micca Longo, 1,2,3S. Longo
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2017.12.001]
1Department of Chemistry, University of Bari, via Orabona 4, Bari, 70126, Italy
2CNR-Nanotec, via Amendola 122/D, Bari, 70126, Italy
3INAF-Osservatorio Astrofisico di Arcetri, Largo E. Fermi 5, Firenze, I-50125, Italy
Copyright Elsevier

Current models allow to reliably simulate mechanical and thermal phenomena associated with a micrometeor passage through the Earth’s atmosphere. However, these models have rarely been applied to materials other than those most common in meteorites, such as silicates and metals. A particular case that deserves attention is the one of micrograins made of minerals, in particular carbonates, which have been associated, in meteorites, with organic molecules. Carbonates are known for their decomposition in vacuum at moderate temperatures, and they might contribute to the thermal protection of organic matter. In this work, a model with non isothermal atmosphere, power balance, evaporation, ablation, radiation losses and stoichiometry, is proposed. This paper includes the very first calculations for meteoroids with a mixed carbonate composition. Results show that the carbonate fraction of these objects always go to zero at high altitudes except for grazing entries, where the reached temperature is lower and some carbonate remains unreacted. For all entry conditions, peculiar temperature curves are obtained due to the decomposition process. Furthermore, a significant impact of decomposition cooling on the temperature peak is observed for some grazing entry cases. Although specific solutions used in these calculations can be improved, this work sets a definite model and a basis for future research on sub-mm grains of relatively volatile minerals entering the Earth’s atmosphere.

Air penetration enhances fragmentation of entering meteoroids

1M. E. Tabetah,1H. J. Melosh
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.13034]
1EAPS Department, Purdue University, West Lafayette, Indiana, USA
Published by arrangement with John Wiley & Sons

The entry and subsequent breakup of the ~17–20 m diameter Chelyabinsk meteoroid deposited approximately 500 kT of TNT equivalent energy to the atmosphere, causing extensive damage that underscored the hazard from small asteroid impacts. The breakup of the meteoroid was characterized by intense fragmentation that dispersed most of the original mass. In models of the entry process, the apparent mechanical strength of the meteoroid during fragmentation, ~1–5 MPa, is two orders of magnitude lower than the mechanical strength of the surviving meteorites, ~330 MPa. We implement a two-material computer code that allows us to fully simulate the exchange of energy and momentum between the entering meteoroid and the interacting atmospheric air. Our simulations reveal a previously unrecognized process in which the penetration of high-pressure air into the body of the meteoroid greatly enhances the deformation and facilitates the breakup of meteoroids similar to the size of Chelyabinsk. We discuss the mechanism of air penetration that accounts for the bulk fragmentation of an entering meteoroid under conditions similar to those at Chelyabinsk, to explain the surprisingly low values of the apparent strength of the meteoroid during breakup.

Mineralogy of the Urvara-Yalode region on Ceres

1A.Longobardo et al. (>10)
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2017.12.011]
1INAF-IAPS, via Fosso del Cavaliere 100, I-00133 Rome, Italy
Copyright Elsevier

We studied the distribution in the Urvara-Yalode region of Ceres (latitudes 21-66°S, longitudes 180-360°E) of main spectral parameters derived from the VIR imaging spectrometer onboard the NASA/Dawn spacecraft, as an overall study of Ceres mineralogy reported in this special issue. In particular, we analyzed the distribution of reflectance at 1.2 μm, band depth at 2.7 and 3.1 μm, ascribed to magnesium and ammoniated phyllosilicates, respectively.

Whereas the average band depths of this region are lower than eastern longitudes, reflecting the E-W dichotomy of abundance of phyllosilicates on Ceres, spectral variations inside this region are observed in the following units: a) the central peak of the Urvara crater (45.9°S, 249.2°E, 170 km in diameter), showing a deep 3.1 μm band depth, indicating an ammonium enrichment; b) the cratered terrain westwards of the Yalode basin (42.3°S, 293.6°E, 260 km in diameter), where absorption bands are deeper, probably due to absence of phyllosilicates depletion following the Yalode impact; c) the hummocky cratered floor of Yalode and Besua (42.4°S, 300.2°E) craters, characterized by lower albedo and band depths, probably due to different roughness; d) Consus (21°S 200°E) and Tawals (39.1°S, 238°E) craters, whose albedo and band depths decreasing could be associated to different grain size or abundance of dark materials. Twenty-two small scale (i.e., lower than 400 m) bright spots are observed: because their composition is similar to the Ceres average, a strong mixing may have occurred since their formation.

Iron Distribution of the Moon Observed by the Kaguya Gamma-ray Spectrometer: Geological Implications for the South Pole-Aitken Basin, the Orientale Basin, and the Tycho Crater.

1M. Naito, 1,2N. Hasebe, 2H. Nagaoka, 2E. Shibamura, 3M. Ohtake, 4K.J. Kim, 5C. Wöhler, 6A.A. Berezhnoy
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2017.12.005]
1School of Advanced Science and Engineering, Waseda University, Japan
2Research Institute for Science and Engineering, Waseda University, Japan
3Institute of Space and Astronautical Science, Japan Aerospace Exploration Agency, Japan
4Korea Institute of Geoscience and Mineral Resources, South Korea
5Image Analysis Group, TU Dortmund University, Germany
6Sternberg Astronomical Institute, Moscow State University, Russia
Copyright Elsevier

In this study we describe the distribution of iron on the Moon as obtained by the Kaguya high energy resolution gamma-ray spectrometer (KGRS). We achieved for the first time the identification of iron based on the fast neutron flux obtained by the KGRS. The iron distribution obtained by KGRS is compared to that of the Lunar Prospector Gamma-Ray Spectrometer (LP GRS), showing that the FeO distributions observed by KGRS and LP GRS, in general, are in good agreement. Furthermore, we compare the iron content data obtained by KGRS and LP GRS to spectral reflectance measurements of the Clementine, Kaguya and Chandrayaan-1 spacecraft as well as those inferred from returned samples. We found differences in FeO concentration and distribution in areas of moderate abundance (6-15 wt%) of the South Pole-Aitken basin, Mare Orientale, and around the crater Tycho crater. It implies that high concentrations of FeO at Mare Ingenii in the South Pole-Aitken basin and Mare Orientale are due to the presence of mare basalts, whereas the enriched FeO content in the central depression of the South Pole-Aitken basin and the Tycho crater indicates the presence of mafic materials such as impact melt breccia.