Mineralogy, reflectance spectra, and physical properties of the Chelyabinsk LL5 chondrite – insight into shock-induced changes in asteroid regoliths

Tomas Kohouta,b,*, Maria Gritsevichc,d,e, Victor I. Grokhovskyf, Grigoriy A. Yakovlevf, Jakub Halodag,h, Patricie Halodovag, Radoslaw M. Michalliki, Antti Penttiläa, Karri Muinonena,c

aDepartment of Physics, University of Helsinki, P.O. Box 64, 00014 Helsinki University, Finland
bInstitute of Geology, Academy of Sciences of the Czech Republic, Rozvojová 269, 16500 Prague 6, Czech Republic
cFinnish Geodetic Institute, Geodeetinrinne 2, P.O. Box 15, FI-02431 Masala, Finland
dInstitute of Mechanics, Lomonosov Moscow State University, Michurinsky prt., 1, 119192, Moscow, Russia
eRussian Academy of Sciences, Dorodnicyn Computing Centre, Department of Computational Physics, Vavilova ul. 40, 119333 Moscow, Russia
fUral Federal University, Ekaterinburg, Russia
gCzech Geological Survey, Geologická 6, 152 00 Praha 5, Czech Republic
hOxford Instruments NanoAnalysis, Halifax Road, High Wycombe, Bucks, HP12 3SE, United Kingdom
iDepartment of Geosciences and Geography, University of Helsinki, P.O. Box 64, 00014 Helsinki University, Finland

The mineralogy and physical properties of Chelyabinsk meteorites (fall, February 15, 2013) are presented. Three types of meteorite material are present, described as the light-colored, dark-colored, and impact-melt lithologies. All are of LL5 composition with the impact-melt lithology being close to whole-rock melt and the dark-colored lithology being shock-darkened due to partial melting of iron metal and sulfides. This enables us to study the effect of increasing shock on material with identical composition and origin. Based on the magnetic susceptibility, the Chelyabinsk meteorites are richer in metallic iron as compared to other LL chondrites. The measured bulk and grain densities and the porosity closely resemble other LL chondrites. Shock-darkening does not have a significant effect on the material physical properties, but causes a decrease of reflectance and decrease in silicate absorption bands in the reflectance spectra. This is similar to the space weathering effects observed on asteroids. However, compared to space weathered materials, there is a negligible to minor slope change observed in impact-melt and shock-darkened meteorite spectra. Thus, it is possible that some dark asteroids with invisible silicate absorption bands may be composed of relatively fresh shock-darkened chondritic material.

Reference
Kohout T, Gritsevich M, Grokhovsky VI, Yakovlev GA, Haloda J, Halodova P, Michallik RM, Penttilä A and Muinonen K (in press) Mineralogy, reflectance spectra, and physical properties of the Chelyabinsk LL5 chondrite – insight into shock-induced changes in asteroid regoliths. Icarus
[doi:10.1016/j.icarus.2013.09.027]
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Evidence for water ice on the moon: Results for anomalous polar craters from the LRO Mini-RF imaging radar

P. D. Spudis1,*, D. B. J. Bussey2, S. M. Baloga3, J. T. S. Cahill2, L. S. Glaze4, G. W. Patterson2, R. K. Raney2, T. W. Thompson5, B. J. Thomson6, E. A. Ustinov5

1Lunar and Planetary Institute, Houston, Texas, USA
2Johns Hopkins University Applied Physics Laboratory, Laurel, Maryland, USA
3Proxemy Research, Laytonsville, Maryland, USA
4NASA Goddard Spaceflight Center, Greenbelt, Maryland, USA
5Jet Propulsion Laboratory, California Institute of Technology, Pasadena, California, USA
6Center for Remote Sensing, Boston University, Boston, Massachusetts, USA

The Mini-RF radar instrument on the Lunar Reconnaissance Orbiter spacecraft mapped both lunar poles in two different RF wavelengths (complete mapping at 12.6 cm S-band and partial mapping at 4.2 cm X-band) in two look directions, removing much of the ambiguity of previous Earth- and spacecraft-based radar mapping of the Moon’s polar regions. The poles are typical highland terrain, showing expected values of radar cross section (albedo) and circular polarization ratio (CPR). Most fresh craters display high values of CPR in and outside the crater rim; the pattern of these CPR distributions is consistent with high levels of wavelength-scale surface roughness associated with the presence of block fields, impact melt flows, and fallback breccia. A different class of polar crater exhibits high CPR only in their interiors, interiors that are both permanently dark and very cold (less than 100 K). Application of scattering models developed previously suggests that these anomalously high-CPR deposits exhibit behavior consistent with the presence of water ice. If this interpretation is correct, then both poles may contain several hundred million tons of water in the form of relatively “clean” ice, all within the upper couple of meters of the lunar surface. The existence of significant water ice deposits enables both long-term human habitation of the Moon and the creation of a permanent cislunar space transportation system based upon the harvest and use of lunar propellant.

Reference
Spudis PD, Bussey DBJ, Baloga SM. Cahill JTS, Glaze LS, Patterson GW, Raney RK, Thompson TW, Thomson BJ and Ustinov EA (in press) Evidence for water ice on the moon: Results for anomalous polar craters from the LRO Mini-RF imaging radar. Journal of Geophysical Research – Planets, 118
[doi:10.1002/jgre.20156]
Published by arrangement with John Wiley & Sons

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Thermal and Collisional History of Tishomingo: More evidence for early disruption of differentiated planetesimals

Jijin Yanga,e,*, Joseph I. Goldsteina, Edward R.D. Scottb, Paul G. Kotulac, Ansgar Grimbergd, Ingo Leyad

aDept. of Mechanical and Industrial Engineering, University of Massachusetts, Amherst, MA 01003, USA
bHawaii Institute of Geophysics and Planetology, University of Hawaii at Manoa, Honolulu, HI 96822, USA
cMaterials Characterization Dept., Sandia National Laboratories, Albuquerque, NM 87185, USA
dPhysical Institute , Universität Bern, CH-3012 Bern, Switzerland
eCarl Zeiss Microscopy, One Zeiss Drive, Thornwood, NY 10594, USA

Tishomingo is a chemically and structurally unique iron with 32.5 wt.% Ni that contains 20% residual taenite and 80% martensite plates, which formed on cooling to between -75 and -200 °C, probably the lowest temperature recorded by any meteorite. Our studies using transmission (TEM) and scanning electron microscopy (SEM), x-ray microanalysis (AEM) and electron backscatter diffraction (EBSD) show that martensite plates in Tishomingo formed in a single crystal of taenite and decomposed during reheating forming 10-100 nm taenite particles with ~50 wt.% Ni, kamacite with ~4 wt.% Ni, along with martensite or taenite with 32 wt.% Ni. EBSD data and experimental constraints show that Tishomingo was reheated to 320-400 °C for about a year transforming some martensite to kamacite and to taenite particles and some martensite directly to taenite without composition change. Fizzy-textured intergrowths of troilite, kamacite with 2.7 wt.% Ni and 2.6 wt.% Co, and taenite with 56 wt.% Ni and 0.15 wt.% Co formed by localized shock melting. A single impact probably melted the sub-mm sulfides, formed stishovite, and reheated and decomposed the martensite plates. Tishomingo and its near-twin Willow Grove, which has 28 wt.% Ni, differ from IAB-related irons like Santa Catharina and San Cristobal that contain 25-36 wt.% Ni, as they are highly depleted in moderately volatile siderophiles and enriched in Ir and other refractory elements. Tishomingo and Willow Grove therefore resemble IVB irons but are chemically distinct. The absence of cloudy taenite in these two irons shows that they cooled through 250 °C abnormally fast at >0.01 °C/yr. Thus this grouplet, like the IVA and IVB irons, suffered an early impact that disrupted their parent body when it was still hot. Our noble gas data show that Tishomingo was excavated from its parent body about 100 to 200 Myr ago and exposed to cosmic rays as a meteoroid with a radius of ~50-85 cm.

Reference
Yang J, Goldstein JI, Scott ERD, Kotula PG, Grimberg A and Leya I (in press) Thermal and Collisional History of Tishomingo: More evidence for early disruption of differentiated planetesimals. Geochimica et Cosmochimica Acta
[doi:10.1016/j.gca.2013.09.023]
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Calibration of cosmogenic noble gas production in ordinary chondrites based on 36Cl-36Ar ages. Part 1: Refined produced rates for cosmogenic 21Ne and 38Ar

N. Dalcher1, M. W. Caffee2, K. Nishiizumi3, K. C. Welten3, N. Vogel4,†, R. Wieler4, I. Leya1,*

1Space Sciences and Planetology, University of Bern, Bern, Switzerland
2Department of Physics, PRIME Laboratory, Purdue University, West Lafayette, Indiana, USA
3Space Sciences Laboratory, University of California, Berkeley, California, USA
4Institute of Geochemistry and Petrology, ETH Zurich, Switzerland
†EAWAG, Dübendorf, Switzerland

We measured the concentrations and isotopic compositions of He, Ne, and Ar in bulk samples and metal separates of 14 ordinary chondrite falls with long exposure ages and high metamorphic grades. In addition, we measured concentrations of the cosmogenic radionuclides 10Be,26Al, and 36Cl in metal separates and in the nonmagnetic fractions of the selected meteorites. Using cosmogenic 36Cl and 36Ar measured in the metal separates, we determined 36Cl-36Ar cosmic-ray exposure (CRE) ages, which are shielding-independent and therefore particularly reliable. Using the cosmogenic noble gases and radionuclides, we are able to decipher the CRE history for the studied objects. Based on the correlation 3He/21Ne versus 22Ne/21Ne, we demonstrate that, among the meteorites studied, only one suffered significant diffusive losses (about 35%). The data confirm that the linear correlation 3He/21Ne versus 22Ne/21Ne breaks down at high shielding. Using 36Cl-36Ar exposure ages and measured noble gas concentrations, we determine 21Ne and 38Ar production rates as a function of 22Ne/21Ne. The new data agree with recent model calculations for the relationship between 21Ne and 38Ar production rates and the 22Ne/21Ne ratio, which does not always provide unique shielding information. Based on the model calculations, we determine a new correlation line for 21Ne and 38Ar production rates as a function of the shielding indicator 22Ne/21Ne for H, L, and LL chondrites with preatmospheric radii less than about 65 cm. We also calculated the 10Be/21Ne and 26Al/21Ne production rate ratios for the investigated samples, which show good agreement with recent model calculations.

Reference
Dalcher N, Caffee MW, Nishiizumi K, Welten KC, Vogel N, Wieler R and Leya I (in press) Calibration of cosmogenic noble gas production in ordinary chondrites based on 36Cl-36Ar ages. Part 1: Refined produced rates for cosmogenic 21Ne and 38Ar. Meteoritics & Planetary Science
[doi:10.1111/maps.12203]
Published by arrangement with John Wiley & Sons

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Carbon substitution for oxygen in silicates in planetary interiors

Sabyasachi Sena, Scarlett J. Widgeona,b, Alexandra Navrotskya,b,*, Gabriela Merac, Amir Tavakolib, Emanuel Ionescuc, and Ralf Riedelc

aDepartment of Chemical Engineering and Materials Science and
bPeter A. Rock Thermochemistry Laboratory and Nanomaterials in the Environment, Agriculture, and Technology Organized Research Unit, University of California, Davis, CA 95616
cInstitut für Materialwissenschaft, Technische Universität Darmstadt, D-64287 Darmstadt, Germany

Amorphous silicon oxycarbide polymer-derived ceramics (PDCs), synthesized from organometallic precursors, contain carbon- and silica-rich nanodomains, the latter with extensive substitution of carbon for oxygen, linking Si-centered SiOxC4-x tetrahedra. Calorimetric studies demonstrated these PDCs to be thermodynamically more stable than a mixture of SiO2, C, and silicon carbide. Here, we show by multinuclear NMR spectroscopy that substitution of C for O is also attained in PDCs with depolymerized silica-rich domains containing lithium, associated with SiOxC4-x tetrahedra with nonbridging oxygen. We suggest that significant (several percent) substitution of C for O could occur in more complex geological silicate melts/glasses in contact with graphite at moderate pressure and high temperature and may be thermodynamically far more accessible than C for Si substitution. Carbon incorporation will change the local structure and may affect physical properties, such as viscosity. Analogous carbon substitution at grain boundaries, at defect sites, or as equilibrium states in nominally acarbonaceous crystalline silicates, even if present at levels at 10–100 ppm, might form an extensive and hitherto hidden reservoir of carbon in the lower crust and mantle.

Reference
Sen S Widgeon SJ, Navrotsky A, Mera G, Tavakoli A, Ionescu E and Riedel R (in press) Carbon substitution for oxygen in silicates in planetary interiors. PNAS
[doi:10.1016/j.icarus.2013.09.020]

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Experimental simulation of oxygen isotopic exchange in olivine and implication for the formation of metamorphosed carbonaceous chondrites

Marina A. Ivanova1,*, Cyril A. Lorenz1, Ian A. Franchi2, Andrei Y. Bychkov3, Jeffrey E. Post4

1Vernadsky Institute of Geochemistry of Russian Academy of Sciences, Moscow, Russia
2Planetary and Space Sciences, The Open University, Milton Keynes, UK
3Moscow State University, Moscow, Russia
4National Museum of Natural History, Smithsonian Institution, Washington, District of Columbia, USA

We have conducted hydration–dehydration experiments on terrestrial olivine to investigate the behavior of oxygen isotopic fractionation to test the hypothesis that multiple cycles of aqueous and thermal processing on a parent asteroid comprise a genetic relationship between CM2s and metamorphosed carbonaceous chondrites (MCCs). Two experiments were undertaken. In the first experiment, serpentine was obtained by hydrating terrestrial olivine (Fo90.9) in the laboratory. During this experiment, olivine was reacted with isotopically heavy water (δ18O 21.5‰) at T = 300 °C, PH2O = 300 bar, for 100 days. The oxygen isotopic composition of the experimental serpentine was enriched in 18O (by 10 ‰ in δ18O) due to exchange of oxygen isotopes between olivine and the 18O-rich water. Dehydrated serpentine was then produced during laboratory heating experiment in vacuum, at T = 930 °C, for 1 h. The oxygen isotopic composition of the dehydrated serpentine was enriched in 18O by a further 7 ‰. The net result of the hydration–dehydration process was an enrichment of 18O in the final material by approximately 17‰. The new experimental results suggest that the oxygen isotopic compositions of MCCs of the Belgica-like group, including Dhofar 225 and Dhofar 725, could be derived from those of typical CM2 chondrites via several cycles of hydration–dehydration caused by aqueous alteration and subsequent thermal metamorphism within their parent asteroids.

Reference
Ivanova MA, Lorenz CA, Franchi IA, Bychkov AY and Post JE (in press) Experimental simulation of oxygen isotopic exchange in olivine and implication for the formation of metamorphosed carbonaceous chondrites. Meteoritics & Planetary Science
[doi:10.1111/maps.12204]
Published by arrangement with John Wiley & Sons

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Formation of brucite and cronstedtite-bearing mineral assemblages on Ceres

Mikhail Yu. Zolotov

School of Earth and Space Exploration, Arizona State University, Tempe, AZ 85287-1404, USA

Dwarf planet Ceres is the largest body in the main asteroid belt with a rocky surface and uncertain internal structure. Spectra of Ceres in near- and mid-infrared wavelengths are consistent with the occurrence of brucite, Mg-bearing carbonates, and an Fe-rich phyllosilicate cronstedtite. Spectra of 10 Hygiea and 324 Bamberga imply similar compositions. Here, we considered stabilities of these minerals to constrain their origin. Cronstedtite is most stable at the temperature of ~0 °C at moderately oxidizing aqueous conditions, and at high water/rock ratios. Although cronstedtite could form on planetesimals, the apparent lack of serpentine may indicate its formation by Ceres’ temporary surface solutions. Brucite forms at a low activity of dissolved SiO2, at a low fugacity of CO2, and at highly alkaline pH. Brucite and cronstedtite do not form together and may not form deep in the Ceres’ interior. The absence of Mg serpentine from Ceres’ surface materials and the unlikely occurrence of very olivine-rich rocks do not indicate a formation of brucite through serpentinization of such rocks. Brucite could form by transient near-surface fluids which do not equilibrate with silicates. Temporary fluids could deposit Mg carbonates before, after, or together with brucite at near-surface conditions that favor CO2 degassing. Regardless of Ceres’ internal structure, internal thermal and aqueous processes may not affect cold near-surface layers. Percolation of interior fluids is not consistent with the lack of detection of low-solubility salts. However, impacts of ice-rich targets during the Late Heavy Bombardment could account for transient aqueous environments and unusual surface mineralogies of Ceres, Hygiea, and Bamberga. Brucite and Mg carbonates could have formed through hydration and carbonation of MgO evaporated from silicates. Apparently abundant carbonates may indicate an ample impact oxidation of organic matter, and the occurrence of brucite with cronstedtite may reflect turbulent and disequilibrium environments. Clay-like homogeneous surface materials on Ceres could be gravitationally sorted deposits of impact clouds.

Reference
Zolotov MY (in press) Formation of brucite and cronstedtite-bearing mineral assemblages on Ceres. Icarus
[doi:10.1016/j.icarus.2013.09.020]
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Anhydrous liquid line of descent of Yamato-980459 and evolution of Martian parental magmas

Jennifer F. Rapp1,2,*, David S. Draper1, Cameron M. Mercer3

1Astromaterials Research Office, Astromaterials Research and Exploration Science Directorate, NASA Johnson Space Center, Houston, Texas, USA
2Lunar and Planetary Institute, Houston, Texas, USA
3School of Earth and Space Exploration, Arizona State University, Tempe, Arizona, USA

We report the results of nominally anhydrous equilibrium and fractional crystallization experiments on a synthetic Yamato-980459 (Y98) bulk composition at 0.5 GPa. These experiments allow us to test a suggested fractional crystallization model, calculated using MELTS by Symes et al. (), in which a Y98-like initial liquid yielded a magma closely resembling the bulk composition of QUE 94201. Although the two meteorites cannot be cogenetic owing to their age difference, they are thought to represent bona fide magmatic liquids rather than products of crystal accumulation, as are most Martian basaltic meteorites. Hence, understanding possible petrogenetic links between these types of liquids could be revealing about processes of melting and crystallization that formed the range of Martian basalts. We find that Y98 can, in fact, generate a residual liquid closely resembling QUE, but only after a very different crystallization process, and different degree of crystallization, than that modeled using MELTS. In addition, both the identity and sequence of crystallizing phases are very different between model and experiments. Our fractional crystallization experiments do not produce a QUE-like liquid, and the crystallizing phases are an even poorer match to the MELTS-calculated compositions than in the equilibrium runs. However, residual liquids from our experiments define a liquid line of descent that encompasses bulk compositions of parental melts calculated for several Martian basaltic meteorites, suggesting that the known Martian basaltic meteorites had their ultimate origin from the same or very similar source lithologies. These are, in turn, similar to source rocks modeled by previous studies as products of extensive crystallization of an initial Martian magma ocean.

Reference
Rapp JF, Draper DS and Mercer CM (in press) Anhydrous liquid line of descent of Yamato-980459 and evolution of Martian parental magmas. Meteoritics & Planetary Science
[doi:10.1111/maps.12197]
Published by arrangement with John Wiley & Sons

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R-chondrite bulk-chemical compositions and diverse oxides: Implications for parent-body processes

Junko Isaa,b,*, Alan E. Rubina,b and John T. Wassona,b,c

aInstitute of Geophysics and Planetary Physics, University of California, Los Angeles, CA 90095–1567, USA
bDepartment of Earth and Space Sciences, University of California, Los Angeles, CA 90095–1567, USA
cDepartment of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095–1567, USA

R chondrites are among the most oxidized chondrite groups; they also have the highest Δ17O values known in whole-rock meteorites. We analyzed R chondrites (six Antarctic, four hot-desert) by instrumental neutron-activation analysis. Data for one of the former and three of the latter show large weathering effects, but the remainder show only moderate scatter and permit us to determine trends and mean compositions for the group. Bulk R-chondrite compositions are similar to those in H and L chondrites, but the concentrations of several volatiles, especially Se and Zn, are higher; the more volatile the element, the higher the enrichment in R chondrites relative to H and L.
Petrologic types in R chondrites extend as low as 3.6. We determined olivine compositional distributions and studied opaque oxides in 15 R-chondrite thin sections, including a newly discovered R4 clast in Bencubbin (adding to the diversity of chondritic clasts in this polymict breccia) and an R clast in CM2 Murchison. Opaque oxides in R chondrites include nearly pure magnetite, Al-rich chromite, magnetite-chromite solid solution, nearly pure chromite, and ilmenite. This diverse set of opaque phases reflects differing aqueous-alteration conditions.
The least equilibrated R chondrites contain nearly pure magnetite but the spinels in metamorphosed R chondrites contain additional components (e.g., Cr2O3 and Al2O3 and some minor cations). The NiO content in olivine correlates with the magnetite component in magnetite-chromite solid solution in equilibrated R chondrites and is a function of the degree of oxidation. The absence of metallic Fe in A-881988 and LAP 031156 indicates a high degree of oxidation; the relatively low-FeO (Fa35) olivine in these rocks in part reflects the conversion of Fe2+ to Fe3+ and its partitioning into magnetite. Oxidation trends in R chondrites are affected by both aqueous alteration and thermal metamorphism. The differing degrees of oxidation in this group reflect differences in local environments on the parent asteroid.

Reference
Isa J, Rubin AE and Wassona JT (in press) R-chondrite bulk-chemical compositions and diverse oxides: Implications for parent-body processes. Geochimica et Cosmochimica Acta
[doi:10.1016/j.gca.2013.09.018]
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Lunar Mare Basalts in the Aristarchus Region: Implications for the Stratigraphic Sequence from Clementine UVVIS data

F Zhanga,b,*, Y L Zoua, Zhenga,c, X H Fua and Y C Zhua,b

aNational Astronomical Observatories, Chinese Academy of Sciences, Beijing 100012, China
bUniversity of Chinese Academy of Sciences, Beijing 100049, China
cCenter for Space Science Research, The Hong Kong University of Science and Technology, Hong Kong, China

The Aristarchus region of Oceanus Procellarum is an area concentrated with lunar basalts, which were mainly produced by the last major phase of lunar volcanism on the western nearside. A group of lunar sample and remote sensing scientists have carried out the extensive task of characterization of lunar mare soils with regard to their mineralogical and chemical makeup and regional geologic mapping. Spectral parameters of the high spatial resolution Clementine images are used to identify and define these basalts as different compositional and spectral units. This endeavor is aimed at deciphering the subtle spectral characteristics of mare soils and validating the mapping technique used in this study, together with making statistical analysis of the links between the basalt types with ages in order to provide a further understanding of material types and geologic evolution in the Aristarchus region of the Moon. From the new perspective of mining geologic information in multivariable image-spaces, spectrally distinct 9 high-Ti and 11 low-Ti basalt reference spectra have been distinguished and as a result, more than 70 spectrally and compositionally basaltic units, which range in age from 1.20 b.y. to 3.74 b.y., have been identified. To some extent, a potential relationship between composition and relative age exists in the statistical analysis of the links between spectral types (related with the Clementine ratio colors) of various basalts and ages in this study, which suggests that composition with different states of maturity correlate with age to some extent. The mineralogical characteristics and spectra-age relationship in the Marius Hills region indicate that the early basalts may still be exposed at the surface deposit after prolonged volcanic activity in this region. This may be a result of not being blanketed by later lava flows, or lava extrusions of underlying low-Ti basalts. In addition, stratigraphic analysis also reveals and confirms that TiO2 concentrations appear to vary independently with time, and generally eruptions of TiO2-rich and TiO2-poor basalts have occurred contemporaneously.

Reference
Zhang F, Zou YL, Zheng YC, Fu XH and Zhu YC (in press) Lunar Mare Basalts in the Aristarchus Region: Implications for the Stratigraphic Sequence from Clementine UVVIS data. Icarus
[doi:10.1016/j.icarus.2013.09.011]
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