Accretion of Solid Materials onto Circumplanetary Disks from Protoplanetary Disks

Takayuki Tanigawa1, Akito Maruta2, and Masahiro N. Machida2

1Institute of Low Temperature Science, Hokkaido University, Sapporo 060-0819, Japan
2Department of Earth and Planetary Sciences, Kyushu University, Fukuoka 812-8581, Japan

We investigate the accretion of solid materials onto circumplanetary disks from heliocentric orbits rotating in protoplanetary disks, which is a key process for the formation of regular satellite systems. In the late stage of the gas-capturing phase of giant planet formation, the accreting gas from protoplanetary disks forms circumplanetary disks. Since the accretion flow toward the circumplanetary disks affects the particle motion through gas drag force, we use hydrodynamic simulation data for the gas drag term to calculate the motion of solid materials. We consider a wide range of size for the solid particles (10-2-106 m), and find that the accretion efficiency of the solid particles peaks around 10 m sized particles because energy dissipation of drag with circum-planetary disk gas in this size regime is most effective. The efficiency for particles larger than 10 m becomes lower because gas drag becomes less effective. For particles smaller than 10 m, the efficiency is lower because the particles are strongly coupled with the background gas flow, which prevents particles from accretion. We also find that the distance from the planet where the particles are captured by the circumplanetary disks is in a narrow range and well described as a function of the particle size.

Reference
Tanigawa T, Maruta A and Machida MN (2014) Accretion of Solid Materials onto Circumplanetary Disks from Protoplanetary Disks. The Astrophysical Journal 784:109.
[doi:10.1088/0004-637X/784/2/109]

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Geochemical processes between steel projectiles and silica-rich targets in hypervelocity impact experiments

Matthias Eberta,b, Lutz Hechta,b, Alexander Deutschc, Thomas Kenkmannd, Richard Wirthe and Jasper Berndtf

aMuseum für Naturkunde (MfN), Leibniz-Institut für Evolutions- und Biodiversitätsforschung, Invalidenstraße 43, D-10115 Berlin, Germany
bFreie Universität Berlin (FU Berlin), Institut für Geologische Wissenschaften, Malteserstr. 74-100, D-12249 Berlin, Germany
cInstitut für Planetologie, Westfälische Wilhelms-Universität Münster (WWU), Wilhelm-Klemm-Str. 10, D-48149 Münster, Germany
dInstitut für Geo- und Umweltwissenschaften, Albert-Ludwigs-Universität Freiburg (ALU), Albertstr. 23-B, D-79104 Freiburg, Germany
eHelmholtz-Zentrum Potsdam, Deutsches GeoForschungsZentrum (GFZ), 3.3, Telegrafenberg, D-14473 Potsdam, Germany
fInstitut für Mineralogie, Westfälische Wilhelms-Universität Münster (WWU), Correns-Str. 24, D-48149 Münster, Germany

The possibility of fractionation processes between projectile and target matter is critical with regard to the classification of the impactor type from geochemical analysis of impactites from natural craters. Here we present results of five hypervelocity MEMIN impact experiments (Poelchau et al., 2013) using the Cr-V-Co-Mo-W-rich steel D290-1 as projectile and two different silica-rich lithologies (Seeberger sandstone and Taunus quartzite) as target materials. Our study is focused on geochemical target-projectile interaction occurring in highly shocked and projectile-rich ejecta fragments. In all of the investigated impact experiments, whether sandstone or quartzite targets, the ejecta fragments show (i) shock-metamorphic features e.g., planar-deformation features (PDF) and the formation of silica glasses, (ii) partially melting of projectile and target, and (iii) significant mechanical and chemical mixing of the target rock with projectile material. The silica-rich target melts are strongly enriched in the “projectile tracer elements” Cr, V, and Fe, but have just minor enrichments of Co, W, and Mo. Inter-element ratios of these tracer elements within the contaminated target melts differ strongly from the original ratios in the steel. The fractionation results from differences in the reactivity of the respective elements with oxygen during interaction of the metal melt with silicate melt. Our results indicate that the principles of projectile-target interaction and associated fractionation do not depend on impact energies (at least for the selected experimental conditions) and water-saturation of the target. Partitioning of projectile tracer elements into the silicate target melt is much more enhanced in experiments with a non-porous quartzite target compared with the porous sandstone target. This is mainly the result of higher impact pressures, consequently higher temperatures and longer reaction times at high temperatures in the experiments with quartzite as target material.

Reference
Ebert M, Hecht L, Deutsch A, Kenkmann T, Wirth R and Berndt J (in press) Geochemical processes between steel projectiles and silica-rich targets in hypervelocity impact experiments. Geochimica et Cosmochimica Acta
[doi:10.1016/j.gca.2014.02.034]
Copyright Elsevier

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Orbit and Bulk Density of the OSIRIS-REx Target Asteroid (101955) Bennu

Steven R. Chesleya et al. (>10)*
*Find the extensive, full author and affiliation list on the publishers website.

aJet Propulsion Laboratory, California Institute of Technology, 4800 Oak Grove Drive, Pasadena, CA 91109, USA

The target asteroid of the OSIRIS-REx asteroid sample return mission, (101955) Bennu (formerly 1999RQ36), is a half-kilometer near-Earth asteroid with an extraordinarily well constrained orbit. An extensive data set of optical astrometry from 1999 to 2013 and high-quality radar delay measurements to Bennu in 1999, 2005, and 2011 reveal the action of the Yarkovsky effect, with a mean semimajor axis drift rate View the MathML source or View the MathML source. The accuracy of this result depends critically on the fidelity of the observational and dynamical model. As an example, neglecting the relativistic perturbations of the Earth during close approaches affects the orbit with 3σ significance in da/dt.

The orbital deviations from purely gravitational dynamics allow us to deduce the acceleration of the Yarkovsky effect, while the known physical characterization of Bennu allows us to independently model the force due to thermal emissions. The combination of these two analyses yields a bulk density of View the MathML source, which indicates a macroporosity in the range 40±10% for the bulk densities of likely analog meteorites, suggesting a rubble-pile internal structure. The associated mass estimate is View the MathML source and View the MathML source.

Bennu’s Earth close approaches are deterministic over the interval 1654–2135, beyond which the predictions are statistical in nature. In particular, the 2135 close approach is likely within the lunar distance and leads to strong scattering and numerous potential impacts in subsequent years, from 2175 to 2196. The highest individual impact probability is 9.5×10-5 in 2196, and the cumulative impact probability is 3.7×10-4, leading to a cumulative Palermo Scale of −1.70.

Reference

Chesley et al. (in press) Orbit and Bulk Density of the OSIRIS-REx Target Asteroid (101955) Bennu. Icarus
[doi:10.1016/j.icarus.2014.02.020]
Copyright Elsevier

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Efflorescence as a source of hydrated sulfate minerals in valley settings on Mars

Anna Szynkiewicza,b, David M. Borrokc,b and David T. Vanimand

aEarth and Planetary Sciences, University of Tennessee, 1412 Circle Drive, Knoxville, TN 37996, USA
bGeological Sciences, University of Texas at El Paso, 500 W University Ave., El Paso, TX 79968, USA
cUniversity of Louisiana at Lafayette, 611 McKinley Street, Lafayette, LA 70504, USA
dPlanetary Science Institute, 1700 E Fort Lowell, Tucson, AZ 85719, USA

A distinctive sulfur cycle dominates many geological processes on Mars and hydrated sulfate minerals are found in numerous topographic settings with widespread occurrences on the Martian surface. However, many of the key processes controlling the hydrological transport of sulfur, including sulfur sources, climate and the depositional history that led to precipitation of these minerals, remain unclear. In this paper, we use a model for the formation of sulfate efflorescent salts (Mg–Ca–Na sulfates) in the Rio Puerco watershed of New Mexico, a terrestrial analog site from the semiarid Southwest U.S., to assess the origin and environmental conditions that may have controlled deposition of hydrated sulfates in Valles Marineris on Mars. Our terrestrial geochemical results (View the MathML source of −36.0 to +11.1‰) show that an ephemeral arid hydrological cycle that mobilizes sulfur present in the bedrock as sulfides, sulfate minerals, and dry/wet atmospheric deposition can lead to widespread surface accumulations of hydrated sulfate efflorescences. Repeating cycles of salt dissolution and reprecipitation appear to be major processes that migrate sulfate efflorescences to sites of surface deposition and ultimately increase the aqueous View the MathML source flux along the watershed (average 41,273 metric tons/yr). We suggest that similar shallow processes may explain the occurrence of hydrated sulfates detected on the scarps and valley floors of Valles Marineris on Mars. Our estimates of salt mass and distribution are in accord with studies that suggest a rather short-lived process of sulfate formation (minimum rough estimate ∼100 to 1000 years) and restriction by prevailing arid conditions on Mars.ed.

Reference
Szynkiewicz A, Borrok DM and Vaniman DT (2014) Efflorescence as a source of hydrated sulfate minerals in valley settings on Mars. Earth and Planetary Science Letters 393:14–25.
[doi:10.1016/j.epsl.2014.02.035]
Copyright Elsevier

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Case Study of Magmatic Differentiation Trends on the Moon based on Lunar Meteorite Northwest Africa 773 and Comparison with Apollo 15 Quartz Monzodiorite

Timothy J. Fagan, Daiju Kashima, Yuki Wakabayashi, Akiko Suginohara

Department of Earth Sciences, Waseda University, 1-6-1 Nishiwaseda, Shinjuku, Tokyo 169-8050

Pyroxene and feldspar compositions indicate that most clasts from the Northwest Africa 773 (NWA 773) lunar meteorite breccia crystallized from a common very low-Ti (VLT) mare basalt parental magma on the Moon. An olivine cumulate (OC), with low-Ca and high-Ca pyroxenes and plagioclase feldspar formed during early stages of crystallization, followed by pyroxene gabbro, which is characterized by zoned pyroxene (Fe# = molar Fe/(Fe+Mg) x 100 from ~35 to 90; Ti# = molar Ti/(Ti+Cr) x 100 from ~20 to 99) and feldspar (~An90-95Ab05-10 to An80-85Ab10-16). Late stage lithologies include alkali-poor symplectite consisting of fayalite, hedenbergitic pyroxene and silica, and alkaline-phase-ferroan clasts characterized by K-rich glass and/or K,Ba-feldspar with fayalite and/or pyroxene. Igneous silica only occurs with the alkaline-phase-ferroan clasts. This sequence of clasts represents stages of magmatic evolution along a ferroan-titanian trend characterized by correlated Fe# and Ti# in pyroxene, and a wide range of increase in Fe# and Ti# prior to crystallization of igneous silica.
Clasts of Apollo 15 quartz monzodiorite (QMD) also have pyroxene co-existing with silica, but the QMD pyroxene has more moderate Fe# (~70). Thus, in AFM components (A = Na2O+K2O, M = MgO, F = FeO), the QMD clasts are similar to the terrestrial calc-alkaline trend (silica-enrichment at moderate Fe#), whereas the ferroan-titanian trend is similar to the terrestrial tholeiitic trend (silica-enrichment only after strong increase in Fe#). However, the variations in SiO2-contents of QMD clasts are due to variable mixing of SiO2-rich and FeO-rich immiscible liquids (i.e., not a progressive increase in SiO2). Immiscibility occurred after fractionation of a KREEP-rich parent liquid.
A third trend is based on zoning relations within the NWA 773 OC, where pyroxene Ti# increases at constant Fe# with proximity to intercumulus, incompatible element-rich pockets rich in K,Ba-feldspar and Ca-phosphates. This type of fractionation (increasing refractory trace elements at constant Fe#) in a cumulate parent rock may have been important for generating lunar rocks that combine low Fe# with high incompatible trace element concentrations, such as KREEP basalts and the magnesian suite.
MELTS (Ghiorso and Sack, 1995; Asimow and Ghiorso, 1998) models of one VLT, one low-Ti and two high-Ti mare basalts and one KREEP basalt all show evolution from low to high Fe# residual liquids during fractional crystallization; however strong enrichments in FeO-concentrations are limited to the VLT and low-Ti liquids. In the high-Ti liquids, crystallization of Fe-Ti-oxides prevents enrichment in FeO, and the increases in Fe# are due to depletion of MgO. Fe-Ti-oxide fractionation results in steady silica-enrichment in the high-Ti mare compositions. Intervals of FeO-enrichment on the VLT and low-Ti mare liquid lines of descent are linked to shifts from olivine to pyroxene crystallization. The onset of plagioclase feldspar crystallization limits the depletion of FeO during crystallization of one high-Ti mare basalt and of the KREEP basalt composition modeled.

Reference
Fagan TJ, Kashima D, Wakabayashi Y and Suginohara A (in press) Case Study of Magmatic Differentiation Trends on the Moon based on Lunar Meteorite Northwest Africa 773 and Comparison with Apollo 15 Quartz Monzodiorite. Geochimica et Cosmochimica Acta
[doi:10.1016/j.gca.2014.02.025]
Copyright Elsevier

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An Organic Cosmo-barometer: Distinct Pressure and Temperature Effects for Methyl Substituted Polycyclic Aromatic Hydrocarbons

Wren Montgomery, Jonathan S. Watson, and Mark A. Sephton

Impacts and Astromaterials Research Centre, Department of Earth Science and Engineering, Imperial College London SW7 2AZ, UK

There are a number of key structures that can be used to reveal the formation and modification history of organic matter in the cosmos. For instance, the susceptibility of organic matter to heat is well documented and the relative thermal stabilities of different isomers can be used as cosmothermometers. Yet despite being an important variable, no previously recognized organic marker of pressure exists. The absence of a pressure marker is unfortunate considering our ability to effectively recognize extraterrestrial organic structures both remotely and in the laboratory. There are a wide variety of pressures in cosmic settings that could potentially be reflected by organic structures. Therefore, to develop an organic cosmic pressure marker, we have used state-of-the-art diamond anvil cell (DAC) and synchrotron-source Fourier transform infrared (FTIR) spectroscopy to reveal the effects of pressure on the substitution patterns for representatives of the commonly encountered methyl substituted naphthalenes, specifically the dimethylnaphthalenes. Interestingly, although temperature and pressure effects are concordant for many isomers, pressure appears to have the opposite effect to heat on the final molecular architecture of the 1,5-dimethylnaphthalene isomer. Our data suggest the possibility of the first pressure parameter or “cosmo-barometer” (1,5-dimethylnaphthalene/total dimethylnaphthalenes) that can distinguish pressure from thermal effects. Information can be obtained from the new pressure marker either remotely by instrumentation on landers or rovers or directly by laboratory measurement, and its use has relevance for all cases where organic matter, temperature, and pressure interplay in the cosmos.

Reference
Montgomery W, Watson JS and Sephton MA (2014) An Organic Cosmo-barometer: Distinct Pressure and Temperature Effects for Methyl Substituted Polycyclic Aromatic Hydrocarbons. The Astrophysical Journal 784:98.
[doi:10.1088/0004-637X/784/2/98]

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Consequences of giant impacts in early Mars: Core merging and Martian dynamo evolution

Julien Monteux1 and Jafar Arkani-Hamed2

1Laboratoire de Planétologie et de Géodynamique, Université de Nantes, Nantes, France
2Department of Physics, University of Toronto, Toronto, Ontario, Canada

A giant impact is an increasingly popular explanation for the formation of the northern lowland on Mars. It is plausible that at the impact time both Mars and the impactor were differentiated with solid silicate mantles and liquid iron cores. Such a large impact likely resulted in merging of the cores of both bodies, a process which will have implications on the thermal state of the planet. We model the evolution of the Martian mantle following a giant impact and characterize the thermochemical consequences of the sinking of an impactor’s core as a single diapir. The impact heating and the viscous heating induced during the core merging may affect the early thermal state of Mars during several tens of million years. Our results show that large viscosity contrasts between the impactor’s core and the surrounding mantle silicates can reduce the duration of the merging down to 1 kyr but do not modify the merging temperature. When the viscosity contrast between the diapir and the surrounding silicates is larger than a factor of 1000, the descent of the diapir can lead to some entrainment of the relatively shallow silicates to deepest regions close to the core-mantle boundary. Finally, the direct impact heating of Martian core leads to thermal stratification of the core and kills the core dynamo. It takes on the order of 150–200 Myr to reinitiate a strong dynamo anew. The merging of the impactor’s core with the Martian core only delays the reinitiation of the dynamo for a very short time.

Reference
Monteux J and Arkani-Hamed J (in press) Consequences of giant impacts in early Mars: Core merging and Martian dynamo evolution. Journal of Geophysical Research: Planets
[doi:10.1002/2013JE004587]
Published by arrangement with John Wiley & Sons

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Corrigendum to “Petrographic, chemical and spectroscopic evidence for thermal metamorphism in carbonaceous chondrites I: CI and CM chondrites” [Geochim. Cosmochim. Acta 126 (2014) 284–306]

Eric Tonui1 et al.

1BP Upstream Research and Technology, 501 Westlake Boulevard, Houston, TX 77079, USA

The authors regret the figure captions of Figs. 1, 13, and 14 fail to provide some necessary references. The following sentences are to be added at the end of the captions, respectively.

Fig. 1. Figures b, c, and d adapted from Nakamura (2005).

Fig. 13. Replotted from Hiroi et al. (1996).

Fig. 14. Spectral data of Y-82162, Y-86720, and B-7904 are from Hiroi et al. (1996).

 The authors would like to apologise for any inconvenience caused.

Reference
Tonui E et al. (in press) Corrigendum to “Petrographic, chemical and spectroscopic evidence for thermal metamorphism in carbonaceous chondrites I: CI and CM chondrites” [Geochim. Cosmochim. Acta 126 (2014) 284–306]. Geochimica et Cosmochimica Acta
[doi:10.1016/j.gca.2014.02.022]
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39Ar-40Ar chronology of the enstatite chondrite parent bodies

Jens Hopp1, Mario Trieloff1, Uli Ott2, Ekaterina V. Korochantseva3, Alexey I. Buykin3

1Institut für Geowissenschaften, Universität Heidelberg, Heidelberg, Germany
2Max-Planck-Institut für Chemie, Mainz, Germany
3Vernadsky Institute for Geochemistry, Moscow, Russia

Ar-Ar isochron ages of EL chondrites suggest closure of the K-Ar system at 4.49 ± 0.01 Ga for EL5 and 6 chondrites, and 4.45 ± 0.01 Ga for EL3 MAC 88136. The high-temperature release regimes contain a mixture of radiogenic 40Ar* and trapped primordial argon (solar or Q-type) with 40Ar/36ArTR ~ 0, which does not affect the 40Ar budget. The low-temperature extractions show evidence of an excess 40Ar component. The 40Ar/36Ar is 180–270; it is defined by intercept values of isochron regression. Excess 40Ar is only detectable in petrologic types >4/5. These lost most of their primordial 36Ar from low-temperature phases during metamorphism and retrapped excess 40Ar. The origin of this excess 40Ar component is probably related to metamorphic Ar mobilization, homogenization of primordial and in situ radiogenic Ar, and trapping of Ar by distinct low-temperature phases. Ar-Ar ages of EH chondrites are more variable and show clear evidence of a major impact-induced partial resetting at about 2.2 Ga ago or alternatively, prolonged metamorphic decomposition of major K carrier phases. EH impact melt LAP 02225 displayed the highest Ar-Ar isochron age of 4.53 ± 0.01 Ga. This age sets a limit of about 25–45 Ma for the age bias between the K-Ar and U-Pb decay systems.

Reference
Hopp J, Trieloff M, Ott U, Korochantseva EV and Buykin AI (in press) 39Ar-40Ar chronology of the enstatite chondrite parent bodies. Meteoritics & Planetary Science
[doi:10.1111/maps.12243]
Published by arrangement with John Wiley & Sons

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Mid-infrared study of stones from the Sutter’s Mill meteorite

Michel Nuevo1,2, Scott A. Sandford1, George J. Flynn3, Susan Wirick4

1NASA Ames Research Center, MS 245-6, Moffett Field, California, USA
2SETI Institute, Mountain View, California, USA
3Department of Physics, SUNY-Plattsburgh, Plattsburgh, New York, USA
4Center for Advanced Radiation Sources, University of Chicago, Chicago, Illinois, USA

The Sutter’s Mill meteorite fell in northern California on April 22, 2012. Several fragments of the meteorite were recovered, some of them shortly after the fall, others several days later after a heavy rainstorm. In this work, we analyzed several samples of four fragments―SM2, SM12, SM20, and SM30―from the Sutter’s Mill meteorite with two infrared (IR) microscopes operating in the 4000–650 cm−1 (2.5–15.4 μm) range. Spectra show absorption features associated with minerals such as olivines, phyllosilicates, carbonates, and possibly pyroxenes, as well as organics. Spectra of specific minerals vary from one particle to another within a given stone, and even within a single particle, indicating a nonuniform mineral composition. Infrared features associated with aliphatic CH2 and CH3 groups associated with organics are also seen in several spectra. However, the presence of organics in the samples studied is not clear because these features overlap with carbonate overtone bands. Finally, other samples collected within days after the rainstorm show evidence for bacterial terrestrial contamination, which indicates how quickly meteorites can be contaminated on such small scales.

Reference
Nuevo M, Sandford SA, Flynn GJ and Wirick S (in press) Mid-infrared study of stones from the Sutter’s Mill meteorite. Meteoritics & Planetary Science
[doi:10.1111/maps.12269]
Published by arrangement with John Wiley & Sons

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