Formation of unequilibrated R chondrite chondrules and opaque phases

1,2K.E. Miller, 1,2D.S. Lauretta, 2,3,4,5H.C. Connolly Jr., 6E.L. Berger, 7K. Nagashima, 2K. Domanik
Geochimica et Cosmochimica Acta (in Press) Link to Article [http://doi.org/10.1016/j.gca.2017.04.009]
1Space Sciences Division, Southwest Research Institute, San Antonio, TX 78238
2Lunar and Planetary Laboratory, University of Arizona, Tucson, AZ 85721, USA
3Department of Geology, School of Earth and the Environment, Rowan University, 201 Mullica Hill Road, Glassboro, N. J. 08028 USA
4Earth and Environmental Sciences, The Graduate Center of the City University of New York, Brooklyn, NY 10016, USA
5Earth and Planetary Science, American Museum of Natural History, Central Park West, New York, NY 10024, USA
6GeoControl Systems Inc. – Jacobs JETS – NASA Johnson Space Center, Houston, TX 77058, USA
7Hawai’i Institute of Geophysics and Planetology, University of Hawai’i at Manoa, Honolulu, HI 96822, USA
Copyright Elsevier

Sulfide assemblages are commonly found in chondritic meteorites as small inclusions in the matrix or in association with chondrules. These assemblages are widely hypothesized to form through pre-accretionary corrosion of metal by H2S gas or through parent body processes. We report here on two unequilibrated R chondrite samples that contain large, chondrule-sized sulfide nodules in the matrix. Both samples are from Mount Prestrud (PRE) 95404. Chemical maps and spot and broad-beam electron microprobe analyses (EMPA) were used to assess the distribution, stoichiometry, and bulk composition of sulfide nodules and silicate chondrules in the clasts. Oxygen isotope data were collected via secondary ion mass spectrometry (SIMS) to assess the relationship of chondrules to other chondrite groups. Scanning electron microscopy (SEM), focused ion beam (FIB), and transmission electron microscopy (TEM) analyses were used to assess fine-scale features and identify crystal structures in sulfide assemblages. Thermodynamic models were used to assess the temperature, sulfur fugacity (fS2), total pressure, dust-to-gas ratio, and oxygen fugacity (fO2) conditions during sulfide nodule and chondrule formation.

The unequilibrated clasts include a mixture of type I and type II chondrules, as well as non-porphyritic chondrules. Chondrule oxygen isotopes overlap with ordinary-chondrite chondrules. Sulfide nodules average 200 µm in diameter, have rounded shapes, and are primarily composed of pyrrhotite, pentlandite, and magnetite. Some are deformed around chondrules in a petrologic relationship similar in appearance to compound chondrules. Both nodules and sulfides in chondrules include phosphate inclusions and Cu-rich lamellae, which suggests a genetic relationship between sulfides in chondrules and in the matrix. Ni/Co ratios for matrix and chondrule sulfides are solar, while Fe and Ni are non-solar and inversely related.

We hypothesize that sulfide nodules formed via pre-accretionary melt processes. During chondrule formation, precursors composed of a mixture of silicate and sulfide material were heated to form immiscible melt droplets, which separated and cooled to form Si-rich chondrules and S-rich nodules. Sulfide melt was stabilized by a high total pressure (∼1 atm) in a dust- or ice-enriched environment. Heating of this material contributed to a high fS2 (2 × 10-3 atm at 1138 °C), and high fO2 (IW – 1 to IW – 4), in an environment with peak temperatures between 1539 °C and 1750 °C. Oxygen isotopic compositions in this region were similar to those recorded by the LL-chondrite chondrules.

The role of sulfides in the fractionation of highly siderophile and chalcophile elements during the formation of martian shergottite meteorites

1Raphael J. Baumgartner, 1Marco L. Fiorentini, 2Jean-Pierre Lorand, 3,4David Baratoux, 5Federica Zaccarini, 6Ludovic Ferrière, 7Marko K. Prašek,8Kerim Sener
Geochimica et Cosmochimica Acta (in Press) Link to Article [http://doi.org/10.1016/j.gca.2017.04.011]
1Centre for Exploration Targeting, School of Earth Sciences, ARC Centre of Excellence for Core to Crust Fluid Systems, University of Western Australia, 6009 Crawley, Australia
2Laboratoire de Planétologie et Géodynamique de Nantes, Université de Nantes and Centre National de la Recherche Scientifique, UMR 6112 44322 Nantes, France
3Géosciences Environnement Toulouse, CNRS, IRD and University of Toulouse, 31400 Toulouse, France
4Institut Fondamental d’Afrique Noire Cheikh Anta Diop, 5005 Dakar, Senegal
5Department of Applied Geological Sciences and Geophysics, University of Leoben, 8700 Leoben, Austria
6Natural History Museum Vienna, 1010 Vienna, Austria
7McGill University, Department of Earth and Planetary Sciences, H3A 0E8, Montreal, Canada
8Matrix Exploration Pty Ltd, 6112 Armadale, Australia
Copyright Elsevier

The shergottite meteorites are ultramafic to mafic igneous rocks whose parental magmas formed from partial melting of the martian mantle. This study reports in-situ laser ablation inductively coupled plasma mass spectrometry analyses for siderophile and chalcophile major and trace elements (i.e., Co, Ni, Cu, As, Se, Ag, Sb, Te, Pb, Bi, and the highly siderophile platinum-group elements, PGE: Os, Ir, Ru, Rh, Pt and Pd) of magmatic Fe-Ni-Cu sulfide assemblages from four shergottite meteorites. They include three geochemically similar incompatible trace element- (ITE-) depleted olivine-phyric shergottites (Yamato-980459, Dar al Gani 476 and Dhofar 019) that presumably formed from similar mantle and magma sources, and one distinctively ITE-enriched basaltic shergottite (Zagami). The sulfides in the shergottites have been variably modified by alteration on Earth and Mars, as well as by impact shock-shock related melting/volatilization during meteorite ejection. However, they inherit and retain their magmatic PGE signatures. The CI chondrite-normalized PGE concentration patterns of sulfides reproduce the whole-rock signatures determined in previous studies. These similarities indicate that sulfides exerted a major control on the PGE during shergottite petrogenesis. However, depletions of Pt (and Ir) in sulfide relative to the other PGE suggest that additional phases such discrete Pt-Fe-Ir alloys have played an important role in the concentration of these elements. These alloys are expected to have enhanced stability in reduced and FeO-rich shergottite magmas, and could be a common feature in martian igneous systems. A Pt-rich PGM was found to occur in a sulfide assemblage in Dhofar 019. However, its origin may be related to impact shock-related sulfide melting and volatilisation during meteorite ejection. In the ITE-depleted olivine-phyric shergottites, positive relationships exist between petrogenetic indicators (e.g., whole-rock Mg-number) and most moderately to strongly siderophile and chalcophile elements in sulfides. These variations extend to incompatible elements like Te and Pd. The whole-rock concentrations of Pd derived from mass-balance calculations decrease by one order of magnitude in the order Y-980459, DaG 476 and Dhofar 019, and broadly overlap the trends in previously published whole-rock analyses. Mantle heterogeneities, and the timing of sulfide saturation as function of mantle melting and/or magma fractionation following ascent from the mantle, may have been the controlling factors of the siderophile and chalcophile element systematics in the analyzed shergottites.

The origin of volatile element depletion in early solar system material: Clues from Zn isotopes in chondrules

1Emily A. Pringle, 1,2Frédéric Moynier, 2,3Pierre Beck, 4Randal Paniello, 5,6Dominik C. Hezel
Earth and Planetary Science Letters 468. 62-71 Link to Article [http://doi.org/10.1016/j.epsl.2017.04.002]
1Institut de Physique du Globe de Paris, Université Paris Diderot, Sorbonne Paris Cité, CNRS UMR 7154, 1 rue Jussieu, 75238 Paris, France
2Institut Universitaire de France, Paris, France
3Institut d’Astrophysique et de Planétologie de Grenoble, Université Grenoble Alpes, France
4Department of Earth and Planetary Sciences, Washington University in St. Louis, USA
5University of Cologne, Department of Geology and Mineralogy, Zülpicher Str. 49b, 50674 Köln, Germany
6Department of Mineralogy, Natural History Museum, Cromwell Road, London, SW7 5BD, UK
Copyright Elsevier

Volatile lithophile elements are depleted in the different planetary materials to various degrees, but the origin of these depletions is still debated. Stable isotopes of moderately volatile elements such as Zn can be used to understand the origin of volatile element depletions. Samples with significant volatile element depletions, including the Moon and terrestrial tektites, display heavy Zn isotope compositions (i.e. enrichment of 66Zn vs. 64Zn), consistent with kinetic Zn isotope fractionation during evaporation. However, Luck et al. (2005) found a negative correlation between δ66Zn and 1/[Zn] between CI, CM, CO, and CV chondrites, opposite to what would be expected if evaporation caused the Zn abundance variations among chondrite groups.

We have analyzed the Zn isotope composition of multiple samples of the major carbonaceous chondrite classes: CI (1), CM (4), CV (2), CO (4), CB (2), CH (2), CK (4), and CK/CR (1). The bulk chondrites define a negative correlation in a plot of δ66Zn vs 1/[Zn], confirming earlier results that Zn abundance variations among carbonaceous chondrites cannot be explained by evaporation. Exceptions are CB and CH chondrites, which display Zn systematics consistent with a collisional formation mechanism that created enrichment in heavy Zn isotopes relative to the trend defined by CI–CK.

We further report Zn isotope analyses of chondrite components, including chondrules from Allende (CV3) and Mokoia (CV3), as well as an aliquot of Allende matrix. All chondrules are enriched in light Zn isotopes (∼500 ppm on 66Zn/64Zn) relative to the bulk, contrary to what would be expected if Zn were depleted during evaporation, on the other hand the matrix has a complementary heavy isotope composition. We report sequential leaching experiments in un-equilibrated ordinary chondrites, which show sulfides are isotopically heavy compared to silicates and the bulk meteorite by ca. +0.65 per mil on 66Zn/64Zn. We suggest isotopically heavy sulfides were removed from either chondrules or their precursors, thereby producing the light Zn isotope enrichments in chondrules.

Primordial and cosmogenic noble gases in the Sutter’s Mill CM chondrite

1Ryuji Okazaki, 2,3Keisuke Nagao
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.12819]
1Faculty of Sciences, Department of Earth and Planetary Sciences, Kyushu University, Nishi-ku, Fukuoka, Japan
2Graduate School of Science, Geochemical Research Center, University of Tokyo, Hongo, Bunkyo-ku, Tokyo, Japan
3Korea Polar Research Institute, Incheon, Yeonsu-gu, South Korea
Published by arrangement with John Wiley & Sons

The Sutter’s Mill (SM) CM chondrite fell in California in 2012. The CM chondrite group is one of the most primitive, consisting of unequilibrated minerals, but some of them have experienced complex processes occurring on their parent body, such as aqueous alteration, thermal metamorphism, brecciation, and solar wind implantation. We have determined noble gas concentrations and isotopic compositions for SM samples using a stepped heating gas extraction method, in addition to mineralogical observation of the specimens. The primordial noble gas abundances, especially the P3 component trapped in presolar diamonds, confirm the classification of SM as a CM chondrite. The mineralogical features of SM indicate that it experienced mild thermal alteration after aqueous alteration. The heating temperature is estimated to be 500 °C. The variation in the heating temperature of thermal alteration is consistent with the texture as a breccia. The heterogeneous distribution of solar wind noble gases is also consistent with it. The cosmic-ray exposure (CRE) age for SM is calculated to be 0.059 ± 0.023 Myr based on cosmogenic 21Ne by considering trapped noble gases as solar wind, the terrestrial atmosphere, P1 (or Q), P3, A2, and G components. The CRE age lies at the shorter end of the CRE age distribution of the CM chondrite group.

Annama H chondrite—Mineralogy, physical properties, cosmic ray exposure, and parent body history

1,2,3Tomáš Kohout et al (>10)*
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.12871]
1Department of Physics, University of Helsinki, Finland
2Institute of Geology, The Czech Academy of Sciences, Praha, Czech Republic
3Finnish Fireball Network, Finland
*Find the extensive, full author and affiliation list on the publishers website
Published by arrangement with John Wiley & Sons

The fall of the Annama meteorite occurred early morning (local time) on April 19, 2014 on the Kola Peninsula (Russia). Based on mineralogy and physical properties, Annama is a typical H chondrite. It has a high Ar-Ar age of 4.4 Ga. Its cosmic ray exposure history is atypical as it is not part of the large group of H chondrites with a prominent 7–8 Ma peak in the exposure age histograms. Instead, its exposure age is within uncertainty of a smaller peak at 30 ± 4 Ma. The results from short-lived radionuclides are compatible with an atmospheric pre-entry radius of 30–40 cm. However, based on noble gas and cosmogenic radionuclide data, Annama must have been part of a larger body (radius >65 cm) for a large part of its cosmic ray exposure history. The 10Be concentration indicates a recent (3–5 Ma) breakup which may be responsible for the Annama parent body size reduction to 30–35 cm pre-entry radius.

Type 1 aqueous alteration in CM carbonaceous chondrites: Implications for the evolution of water-rich asteroids

1A. J. King, 1P. F. Schofield, 1S. S. Russell
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.12872]
1Department of Earth Sciences, Natural History Museum, London, UK
Published by arrangement with John Wiley & Sons

The CM carbonaceous chondrite meteorites experienced aqueous alteration in the early solar system. They range from mildly altered type 2 to almost completely hydrated type 1 chondrites, and offer a record of geochemical conditions on water-rich asteroids. We show that CM1 chondrites contain abundant (84–91 vol%) phyllosilicate, plus olivine (4–8 vol%), magnetite (2–3 vol%), Fe-sulfide (120 °C), although higher water/rock ratios may also have played a role. The modal data provide constraints for interpreting the composition of asteroids and the mineralogy of samples returned from these bodies. We predict that “CM1-like” asteroids, as has been proposed for Bennu—target for the OSIRIS-REx mission—will have a high abundance of Mg-rich phyllosilicates and Fe-oxides, but be depleted in calcite.

Update (2012–2017) on lunar meteorites from Oman

1Randy L. Korotev
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.12869]
1Department of Earth and Planetary Sciences and McDonnell Center for the Space Sciences, Washington University, St. Louis, Missouri, USA
Published by arrangement with John Wiley & Sons

This report presents bulk composition data for 10 lunar meteorite stones from Oman for which the names have been approved since June, 2012. On the basis of composition and reported find location, four new meteorites are represented among this group of stones. Data from neutron activation analysis of 371 subsamples of all lunar meteorites from Oman and Saudi Arabia analyzed in this laboratory are presented.

Unmelted cosmic metal particles in the Indian Ocean

1Mokkapati Shyam Prasad, 1N. G. Rudraswami, 1Agnelo A. De Araujo, 1Vijay D. Khedekar
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.12858]
1CSIR-National Institute of Oceanography, Dona Paula, Goa, India
Published by arrangement with John Wiley & Sons

Fe-Ni metal is a common constituent of most meteorites and is an indicator of the thermal history of the respective meteorites, it is a diagnostic tool to distinguish between groups/subgroups of meteorites. In spite of over a million micrometeorites collected from various domains, reports of pure metallic particles among micrometeorites have been extremely rare. We report here the finding of a variety of cosmic metal particles such as kamacite, plessite, taenite, and Fe-Ni beads from deep-sea sediments of the Indian Ocean, a majority of which have entered the Earth unaffected by frictional heating during atmospheric entry. Such particles are known as components of meteorites but have never been found as individual entities. Their compositions suggest precursors from a variety of meteorite groups, thus providing an insight into the metal fluxes on the Earth. Some particles have undergone heating and oxidation to different levels during entry developing features similar to I-type cosmic spherules, suggesting atmospheric processing of individual kamacites/taenite grains as another hitherto unknown source for the I-type spherules. The particles have undergone postdepositional aqueous alteration transforming finally into the serpentine mineral cronstedtite. Aqueous alteration products of kamacite reflect the local microenvironment, therefore they have the potential to provide information on the composition of water in the solar nebula, on the parent bodies or on surfaces of planetary bodies. Our observations suggest it would take sustained burial in water for tens of thousands of years under cold conditions for kamacites to alter to cronstedtite.

Meteoritic minerals and their origins

1,2Alan E. Rubin, 3Chi Ma
Chemie der Erde – Geochemistry (in Press) Link to Article [http://doi.org/10.1016/j.chemer.2017.01.005]
1Department of Earth, Planetary, and Space Sciences, University of California, Los Angeles, CA 90095-1567, USA
2Institute of Geophysics and Planetary Physics, University of California, Los Angeles, CA 90095-1567, USA
3Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, CA 91125, USA
Copyright Elsevier

About 435 mineral species have been identified in meteorites including native elements, metals and metallic alloys, carbides, nitrides and oxynitrides, phosphides, silicides, sulfides and hydroxysulfides, tellurides, arsenides and sulfarsenides, halides, oxides, hydroxides, carbonates, sulfates, molybdates, tungstates, phosphates and silico phosphates, oxalates, and silicates from all six structural groups. The minerals in meteorites can be categorized as having formed by a myriad of processes that are not all mutually distinct: (1) condensation in gaseous envelopes around evolved stars (presolar grains), (2) condensation in the solar nebula, (3) crystallization in CAI and AOI melts, (4) crystallization in chondrule melts, (5) exsolution during the cooling of CAIs, (6) exsolution during the cooling of chondrules and opaque assemblages, (7) annealing of amorphous material, (8) thermal metamorphism and exsolution, (9) aqueous alteration, hydrothermal alteration and metasomatism, (10) shock metamorphism, (11) condensation within impact plumes, (12) crystallization from melts in differentiated or partially differentiated bodies, (13) condensation from late-stage vapors in differentiated bodies, (14) exsolution, inversion and subsolidus redox effects within cooling igneous materials, (15) solar heating near perihelion, (16) atmospheric passage, and (17) terrestrial weathering.

 

Evidence for OH or H2O on the surface of 433 Eros and 1036 Ganymed

1Andrew S. Rivkin, 2Ellen S. Howell, 3Joshua P. Emery, 4Jessica Sunshine
Icarus (in Press) Link to Article [http://doi.org/10.1016/j.icarus.2017.04.006]
1Johns Hopkins University Applied Physics Laboratory, 11101 Johns Hopkins Rd, Laurel MD, 20723 USA 443-778-2811
2University of Arizona, Lunar and Planetary Laboratory
3University of Tennessee
4University of Maryland
Copyright Elsevier

Water and hydroxyl, once thought to be found only in the primitive airless bodies that formed beyond roughly 2.5-3 AU, have recently been detected on the Moon and Vesta, which both have surfaces dominated by evolved, non-primitive compositions. In both these cases, the water/OH is thought to be exogenic, either brought in via impacts with comets or hydrated asteroids or created via solar wind interactions with silicates in the regolith or both. Such exogenic processes should also be occurring on other airless body surfaces. To test this hypothesis, we used the NASA Infrared Telescope Facility (IRTF) to measure reflectance spectra (2.0 to 4.1 μm) of two large near-Earth asteroids (NEAs) with compositions generally interpreted as anhydrous: 433 Eros and 1036 Ganymed. OH is detected on both of these bodies in the form of absorption features near 3 μm. The spectra contain a component of thermal emission at longer wavelengths, from which we estimate thermal of 167±98 J m−2s−1/2K−1 for Eros (consistent with previous estimates) and 214±80 J m−2s−1/2K−1 for Ganymed, the first reported measurement of thermal inertia for this object. These observations demonstrate that processes responsible for water/OH creation on large airless bodies also act on much smaller bodies.