Silicate liquid immiscibility in impact melts

1,2Christopher Hamann,3Agnese Fazio,4Matthias Ebert,1,2Lutz Hecht,5Richard Wirth,6Luigi Folco,7Alex Deutsch,1,8,9Wolf Uwe Reimold
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.12907]
1Museum für Naturkunde, Leibniz-Institut für Evolutions- und Biodiversitätsforschung, Berlin, Germany
2Institut für Geologische Wissenschaften, Freie Universität Berlin, Berlin, Germany
3Institut für Geowissenschaften, Friedrich-Schiller-Universität Jena, Jena, Germany
4Institut für Geo- und Umweltnaturwissenschaften, Albert-Ludwigs-Universität Freiburg, Freiburg im Breisgau, Germany
5Helmholtz-Zentrum Potsdam—Deutsches GeoForschungsZentrum GFZ, Potsdam, Germany
6Dipartimento di Science della Terra, Università di Pisa, Pisa, Italy
7Institut für Planetologie, Westfälische Wilhelms-Universität Münster, Münster, Germany
8Humboldt-Universität zu Berlin, Berlin, Germany
9Laboratório de Geocronologia, Instituto de Geociências, Universidade de Brasília, Brazil
Published by arrangement with John Wiley & Sons

We have investigated silicate emulsions in impact glasses and impact melt rocks from the Wabar (Saudi Arabia), Kamil (Egypt), Barringer (USA), and Tenoumer (Mauritania) impact structures, and in experimentally generated impact glasses and laser-generated glasses (MEMIN research unit) by scanning electron microscopy, electron microprobe analysis, and transmission electron microscopy. Textural evidence of silicate liquid immiscibility includes droplets of one glass disseminated in a chemically distinct glassy matrix; sharp phase boundaries (menisci) between the two glasses; deformation and coalescence of droplets; and occurrence of secondary, nanometer-sized quench droplets in Si-rich glasses. The compositions of the conjugate immiscible liquids (Si-rich and Fe-rich) are consistent with phase separation in two-liquid fields in the general system Fe2SiO4–KAlSi3O8–SiO2–CaO–MgO–TiO2–P2O5. Major-element partition coefficients are well correlated with the degree of polymerization (NBO/T) of the Si-rich melt: Fe, Ca, Mg, and Ti are concentrated in the poorly polymerized, Fe-rich melt, whereas K, Na, and Si prefer the highly polymerized, Si-rich melt. Partitioning of Al is less pronounced and depends on bulk melt composition. Thus, major element partitioning between the conjugate liquids closely follows trends known from tholeiitic basalts, lunar basalts, and experimental analogs. The characteristics of impact melt inhomogeneity produced by melt unmixing in a miscibility gap are then compared to impact melt inhomogeneity caused by incomplete homogenization of different (miscible or immiscible) impact melts that result from shock melting of different target lithologies from the crater’s melt zone, which do not fully homogenize and equilibrate due to rapid quenching. By taking previous reports on silicate emulsions in impact glasses into account, it follows that silicate impact melts of variable composition, cooling rate, and crystallization history might readily unmix during cooling, thereby rendering silicate liquid immiscibility a much more common process in the evolution of impact melts than previously recognized.

Identification of a primordial asteroid family constrains the original planetesimal population

1Marco Delbo’, 2Kevin Walsh, 1Bryce Bolin, 3Chrysa Avdellidou, 1Alessandro Morbidelli
Science 357, 1026-1029 Link to Article [DOI: 10.1126/science.aam6036]
1Université Côte d’Azur, CNRS–Lagrange, Observatoire de la Côte d’Azur, CS 34229–F 06304 Nice Cedex 4, France.
2Southwest Research Institute, 1050 Walnut Street, Suite 300, Boulder, CO 80302, USA.
3Scientific Support Office, Directorate of Science, European Space Agency, Keplerlaan 1, NL-2201 AZ Noordwijk ZH, Netherlands.
Reprinted with permission from AAAS

A quarter of known asteroids is associated with more than 100 distinct asteroid families, meaning that these asteroids originate as impact fragments from the family parent bodies. The determination of which asteroids of the remaining population are members of undiscovered families, or accreted as planetesimals from the protoplanetary disk, would constrain a critical phase of planetary formation by unveiling the unknown planetesimal size distribution. We discovered a 4-billion-year-old asteroid family extending across the entire inner part of the main belt whose members include most of the dark asteroids previously unlinked to families. This allows us to identify some original planetesimals, which are all larger than 35 kilometers, supporting the view of asteroids being born big. Their number matches the known distinct meteorite parent bodies.

Insights into solar nebula formation of pyrrhotite from nanoscale disequilibrium phases produced by H2S sulfidation of Fe metal

1Zack Gainsforth, 2Dante S. Lauretta, 3Nobumichi Tamura, 1Andrew J. Westphal, 1Christine E. Jilly-Rehak, 1Anna L. Butterworth
American Mineralogist 102, 1881-1893 Link to Article [DOI
https://doi.org/10.2138/am-2017-5848]
1Space Sciences Laboratory, University of California at Berkeley, Berkeley, California 94720, U.S.A.
2Lunar and Planetary Laboratory, University of Arizona, Tucson, Arizona 85721, U.S.A.
3Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, California 94720, U.S.A.
Copyright: The Mineralogical Society of America

Lauretta (2005) produced sulfide in the laboratory by exposing canonical nebular metal analogs to H2S gas under temperatures and pressures relevant to the formation of the Solar System. The resulting reactions produced a suite of sulfides and nanophase materials not visible at the microprobe scale, but which we have now analyzed by TEM for comparison with interplanetary dust samples and comet Wild 2 samples returned by the Stardust mission. We find the unexpected result that disequilibrium formation favors pyrrhotite over troilite and also produces minority schreibersite, daubréelite, barringerite, taenite, oldhamite, and perryite at the metal-sulfide interface. TEM identification of nanophases and analysis of pyrrhotite superlattice reflections illuminate the formation pathway of disequilibrium sulfide. We discuss the conditions under which such disequilibrium can occur, and implications for formation of sulfide found in extraterrestrial materials.

Trace element inventory of meteoritic Ca-phosphates

1Dustin Ward, 1Addi Bischoff, 2Julia Roszjar, 3Jasper Berndt, 4Martin J. Whitehouse
American Mineralogist 102, 1856-1880 Link to Article [DOI
https://doi.org/10.2138/am-2017-6056]
1Institut für Planetologie, Westfälische Wilhelms-Universität Münster, Wilhelm-Klemm-Str. 10, 48149 Münster, Germany
2Department of Mineralogy and Petrography, Natural History Museum Vienna, Burgring 7, 1010 Vienna, Austria
3Institut für Mineralog
ie, Westfälische Wilhelms-Universität Münster, Corrensstrasse 24, 48149 Münster, Germany
4Department of Geosciences, Swedish Museum of Natural History, Box 50007, 10405 Stockholm, Sweden
Copyright: The Mineralogical Society of America

Most extraterrestrial samples feature the two accessory Ca-phosphates (apatite-group minerals and merrillite), which are important carrier phases of the rare earth elements (REE). The trace-element concentrations (REE, Sc, Ti, V, Cr, Mn, Co, As, Rb, Sr, Y, Zr, Nb, Ba, Hf, Ta, Pb, Th, and U) of selected grains were analyzed by LA-ICP-MS and/or SIMS (REE only). This systematic investigation includes 99 apatite and 149 merrillite analyses from meteorites deriving from various asteroidal bodies including 1 carbonaceous chondrite, 8 ordinary chondrites, 3 acapulcoites, 1 winonaite, 2 eucrites, 5 shergottites, 1 ureilitic trachyandesite, 2 mesosiderites, and 1 silicate-bearing IAB iron meteorite.

Although Ca-phosphates predominantly form in metamorphic and/or metasomatic reactions, some are of igneous origin. As late-stage phases that often incorporate the vast majority of their host’s bulk REE budget, the investigated Ca-phosphates have REE enrichments of up to two orders of magnitude compared to the host rock’s bulk concentrations. Within a single sample, each phosphate species displays a uniform REE-pattern, and variations are mainly restricted to their enrichment, therefore indicating similar formation conditions. Exceptions are brecciated samples, i.e., the Adzhi-Bogdo (LL3-6) ordinary chondrite. Despite this uniformity within single samples, distinct meteorite groups do not necessarily have unique REE-patterns. Four basic shapes dominate the REE patterns of meteoritic Ca-phosphates: (1) flat patterns, smoothly decreasing from La-Lu with prominent negative Eu anomalies (acapulcoites, eucrites, apatite from the winonaite and the ureilitic trachyandesite, merrillite from ordinary chondrites); (2) unfractionated patterns, with only minor or no anomalies (mesosiderites, enriched shergottites, IAB-iron meteorite); (3) LREE-enriched patterns, with either positive or slightly negative Eu anomalies (chondritic apatite); and (4) strongly LREE-depleted patterns, with negative Eu anomalies (depleted shergottites). The patterns do not correlate with the grade of metamorphism (petrologic type), specific adjacent mineral assemblages or with Ca-phosphate grain size. Neither the proportions of different REE, nor particular REE patterns themselves are universally correlated to a specific formation mechanism yet Eu (i.e., magnitude of the Eu anomaly) is a sensitive indicator to evaluate the timing of plagioclase and phosphate crystallization. Based on our data, U and Th abundances in apatite increase (almost linearly) with the grade of metamorphism, as well as with the differentiation of their host rock.

Application of spectral linear mixing to rock slabs analyses at various scales using Ma_Miss BreadBoard instrument

1Simone De Angelis, 1Paola Manzari, 1Maria Cristina De Sanctis, 1Francesca Altieri, 1Cristian Carli, 2Giovanna Agrosì
Planetary and Space Science 144 1-15 Link to Article [https://doi.org/10.1016/j.pss.2017.06.005]
1Institute for Space Astrophysics and Planetology, INAF-IAPS, via Fosso del Cavaliere, 100, 00133, Rome, Italy
2University of Bari “Aldo Moro”, Department of Earth and Geoenvironmental Sciences, via Orabona, 4, 70125, Bari, Italy

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Cosmic-ray exposure ages of six chondritic Almahata Sitta fragments

1,2M.E.I.Riebe et al. (>10)
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.12936]
1Institute of Geochemistry and Petrology, ETH Zürich, Zurich, Switzerland
2Department of Terrestrial Magnetism, Carnegie Institution of Washington, Washington, D.C., USA
Published by arrangement with John Wiley & Sons

The Almahata Sitta strewn field is dominated by ureilites, but contains a large fraction of chondritic fragments of various types. We analyzed stable isotopes of He, Ne, Ar, Kr, and Xe, and the cosmogenic radionuclides 10Be, 26Al, and 36Cl in six chondritic Almahata Sitta fragments (EL6 breccia, EL6, EL3-5, CB, LL4/5, R-like). The cosmic-ray exposure (CRE) ages of five of the six samples have an average of 19.2 ± 3.3 Ma, close to the average of 19.5 ± 2.5 Ma for four ureilites. The cosmogenic radionuclide concentrations in the chondrites indicate a preatmospheric size consistent with Almahata Sitta. This corroborates that Almahata Sitta chondrite samples were part of the same asteroid as the ureilites. However, MS-179 has a lower CRE age of 11.0 ± 1.4 Ma. Further analysis of short-lived radionuclides in fragment MS-179 showed that it fell around the same time, and from an object of similar size as Almahata Sitta, making it almost certain that MS-179 is an Almahata Sitta fragment. Instead, its low CRE age could be due to gas loss, chemical heterogeneity that may have led to an erroneous 21Ne production-rate, or, perhaps most likely, MS-179 could represent the true 4π exposure age of Almahata Sitta (or an upper limit thereof), while all other samples analyzed so far experienced exposure on the parent body of similar lengths. Finally, MS-179 had an extraordinarily high activity of neutron-capture 36Cl, ~600 dpm kg−1, the highest activity observed in any meteorite to date, related to a high abundance of the Cl-bearing mineral lawrencite.

The Northwest Africa 8159 Martian Meteorite: Expanding the Martian Sample Suite to the Early Amazonian

Christopher D.K.Herd et al. (>10)
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2017.08.037]
1Department of Earth and Atmospheric Sciences, University of Alberta, Edmonton, Alberta, T6G 2E3, Canada
Copyright Elsevier

Northwest Africa (NWA) 8159 is an augite-rich shergottite, with a mineralogy dominated by Ca-, Fe-rich pyroxene, plagioclase, olivine, and magnetite. NWA 8159 crystallized from an evolved melt of basaltic composition under relatively rapid conditions of cooling, likely in a surface lava flow or shallow sill. Redox conditions experienced by the melt shifted from relatively oxidizing (with respect to known Martian lithologies, ∼QFM) on the liquidus to higher oxygen fugacity (∼QFM+2) during crystallization of the groundmass, and under subsolidus conditions. This shift resulted in the production of orthopyroxene and magnetite replacing olivine phenocryst rims. NWA 8159 contains both crystalline and shock-amorphized plagioclase (An50-62), often observed within a single grain; based on known calibrations we bracket the peak shock pressure experienced by NWA 8159 to between 15 and 23 GPa. The bulk composition of NWA 8159 is depleted in LREE, as observed for Tissint and other depleted shergottites; however, NWA 8159 is distinct from all other martian lithologies in its bulk composition and oxygen fugacity. We obtain a Sm-Nd formation age of 2.37 ± 0.25 Ga for NWA 8159, which represents an interval in Mars geologic time which, until recently, was not represented in the other martian meteorite types. The bulk rock 147Sm/144Nd value of 0.37 ± 0.02 is consistent with it being derived directly from its source and the high initial ε143Nd value indicates this source was geochemically highly depleted. Cr, Nd, and W isotopic compositions further support a unique mantle source. While the rock shares similarities with the 2.4-Ga NWA 7635 meteorite, there are notable distinctions between the two meteorites that suggest differences in mantle source compositions and conditions of crystallization. Nevertheless, the two samples may be launch-paired. NWA 8159 expands the known basalt types, ages and mantle sources within the Mars sample suite to include a second igneous unit from the early Amazonian.

The noble gas concentrations of the Martian meteorites GRV 99027 and paired NWA 7906/NWA 7907

1Peter C. Stephenson,2Yangting Lin,1Ingo Leya
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.12950]
1Physical Institute, Space Sciences and Planetology, University of Bern, Bern, Switzerland
2Key Laboratory of Earth and Planetary Physics, Institute of Geology and Geophysics, Chinese Academy of Sciences, Beijing, China
Published by arrangement with John Wiley & Sons

Here we present the isotopic concentrations of He, Ne, Ar, Kr, and Xe for the three Martian meteorites, namely Grove Mountains 99027 (GRV 99027), Northwest Africa 7906 (NWA 7906), and Northwest Africa 7907 (NWA 7907). The cosmic ray exposure (CRE) age for GRV 99027 of 5.7 ± 0.4 Ma (1σ) is consistent with CRE ages for other poikilitic basaltic shergottites and suggests that all were ejected in a single event ~5.6 Ma ago. After correcting for an estimated variable sodium concentration, the CRE ages for NWA 7906 and NWA 7907 of 5.4 ± 0.4 and 4.9 ± 0.4 Ma (1σ), respectively, are in good agreement with the CRE age of ~5 Ma favored by Cartwright et al. (2014) for NWA 7034. The data, therefore, support the conclusion that all three basaltic regolith breccias are paired. The 40Ar gas retention age for NWA 7907 of ~1.3 Ga is in accord with Cartwright et al. (2014). For NWA 7906, we were unable to determine a 40Ar gas retention age. The 4He gas retention ages for NWA 7906 and 7907 are in the range of 200 Ma and are much shorter than the 40Ar gas retention age of NWA 7907, indicating that about 86–88% of the radiogenic 4He has been lost. The Kr and Xe isotopic concentrations in GRV 99027 are composed almost exclusively of Martian interior (MI) gases, while for NWA 7906 and NWA 7907, they indicate gases from the MI, elementally fractionated air, and possibly Martian atmosphere.

Intermineral oxygen three-isotope systematics of silicate minerals in equilibrated ordinary chondrites

1David McDougal,1,2Daisuke Nakashima,1,3Travis J. Tenner,1Noriko T. Kita,1John W. Valley,4Takaaki Noguchi
Meteoritics & Planetary Science (in Press) Link to Article [DOI: 10.1111/maps.12932]
1WiscSIMS, Department of Geoscience, University of Wisconsin-Madison, Madison, Wisconsin, USA
2Department of Earth and Planetary Material Sciences, Faculty of Science, Tohoku University, Sendai, Miyagi, Japan
3Chemistry Division, Nuclear and Radiochemistry, Los Alamos National Laboratory, Los Alamos, New Mexico, USA
4Faculty of Arts and Science, Kyushu University, Fukuoka, Japan
Published by arrangement with John Wiley & Sons

High-precision oxygen three-isotope ratios were measured for four mineral phases (olivine, low-Ca and high-Ca pyroxene, and plagioclase) in equilibrated ordinary chondrites (EOCs) using a secondary ion mass spectrometer. Eleven EOCs were studied that cover all groups (H, L, LL) and petrologic types (4, 5, 6), including S1–S4 shock stages, as well as unbrecciated and brecciated meteorites. SIMS analyses of multiple minerals were made in close proximity (mostly <100 μm) from several areas in each meteorite thin section, to evaluate isotope exchange among minerals. Oxygen isotope ratios in each mineral become more homogenized as petrologic type increases with the notable exception of brecciated samples. In type 4 chondrites, oxygen isotope ratios of olivine and low-Ca pyroxene are heterogeneous in both δ18O and Δ17O, showing similar systematics to those in type 3 chondrites. In type 5 and 6 chondrites, oxygen isotope ratios of the four mineral phases plot along mass-dependent fractionation lines that are consistent with the bulk average Δ17O of each chondrite group. The δ18O of three minerals, low-Ca and high-Ca pyroxene and plagioclase, are consistent with equilibrium fractionation at temperatures of 700–1000 °C. In most cases the δ18O values of olivine are higher than those expected from pyroxene and plagioclase, suggesting partial retention of premetamorphic values due to slower oxygen isotope diffusion in olivine than pyroxene during thermal metamorphism in ordinary chondrite parent bodies.