Spectro-chemical study of moldavites from Ries impact structure (Germany) using LIBS

1Abhishek K.Rai,1,2Jayanta K.Pati,3Rohit Kumar
Optics&Laser Technology 114, 146-157 Link to Article [https://doi.org/10.1016/j.optlastec.2019.01.028]
1Department of Earth and Planetary Sciences, Nehru Science Centre, University of Allahabad, Allahabad 211 002, India
2National Center of Experimental Mineralogy and Petrology, 14, Chatham Lines, University of Allahabad, Allahabad 211 002, India
3Department of Physics, C.M.P. Degree College, University of Allahabad, Allahabad 211 002, India

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Allabogdanite, the high-pressure polymorph of (Fe,Ni)2P, a stishovite-grade indicator of impact processes in the Fe–Ni–P system

1,2Sergey N. Britvin,3Vladimir V. Shilovskikh,4Renato Pagano,3Natalia S. Vlasenko,5Anatoly N. Zaitsev,5Maria G. Krzhizhanovskaya,3Maksim S. Lozhkin,5Andrey A. Zolotarev,5Vladislav V. Gurzhiy
Scientific Reports 9, 1047 Link to Article [https://doi.org/10.1038/s41598-018-37795-x]
1Institute of Earth Sciences, Saint-Petersburg State University, Universitetskaya Nab. 7/9, 199034, St. Petersburg, Russia
2Kola Science Center of Russian Academy of Sciences, Fersman Str. 14, 184209, Apatity, Murmansk Region, Russia
3Centre for Geo-Environmental Research and Modelling, Saint-Petersburg State University, Ulyanovskaya ul. 1, 198504, St. Petersburg, Russia
4Casella Postale 37, Cinisello, Milano, Italy
5Institute of Earth Sciences, Saint-Petersburg State University, Universitetskaya Nab. 7/9, 199034, St. Petersburg, Russia

 

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Sticking Properties of Silicates in Planetesimal Formation Revisited

Tobias Steinpilz, Jens Teiser, and Gerhard Wurm
Astrophysical Journal 874, 60 Link to Article [DOI: 10.3847/1538-4357/ab07bb ]
University of Duisburg-Essen, Faculty of Physics, Lotharstr. 1-21D, Duisburg 47057, Germany

In the past, laboratory experiments and theoretical calculations showed a mismatch in the derived sticking properties of silicates in the context of planetesimal formation. It has been proposed by Kimura et al. that this mismatch is due to the value of the surface energy assumed, supposedly correlated to the presence or lack of water layers of different thickness on a grain’s surface. We present tensile strength measurements of dust aggregates with different water content here. The results are in support of the suggestion by Kimura et al. Dry samples show increased strengths by a factor of up to 10 over wet samples. A high value of γ = 0.2 J m−2 likely applies to the dry low pressure conditions of protoplanetary disks and should be used in the future.

The r-process with the Newly Developed High-precision Mass Model WS4

B. Zhao (赵斌)1 and S. Q. Zhang (张双全)2
Astrophysical Journal 874, 5 Link to Article [DOI: 10.3847/1538-4357/ab0702 ]
1School of Physics and Nuclear Energy Engineering, Beihang University Beijing 100191, People’s Republic of China
2School of Physics, Peking University, Beijing 100871, People’s Republic of China

The influence of the new mass model Weizsäcker–Skyrme 4 (WS4) on the r-process abundance distribution is investigated using the site-independent classical r-process and the site-dependent dynamical r-process models. The dynamical r-process calculations are performed under the neutrino-driven wind scenario. In comparison with the finite-range droplet model (FRDM) often used in r-process calculations, better agreement between the calculated abundance and the observed solar r-process abundance is found in both the classical and dynamical calculations by using the mass model WS4. The abundance underestimations at the A ~ 115, 140, and 200 mass regions encountered with the calculations using the FRDM is overcome to a large extent by using WS4.

Effect of silicon on activity coefficients of Bi, Cd, Sn, and Ag in liquid Fe‐Si, and implications for differentiation and core formation

1K. Righter,2K. Pando,2D. K. Ross,3M. Righter,3T. J. Lapen
Meteoritics & Planetary Science (in Press) Link to Article [https://doi.org/10.1111/maps.13285]
1NASA JSC, Mailcode XI2, 2101 NASA Pkwy, Houston, Texas, 77058 USA
2UTC–Jacobs JETS Contract, NASA JSC, Houston, Texas, 77058 USA
3Department of Earth and Atmospheric Sciences, University of Houston, Houston, Texas, 77204 USA
Published by arrangement with John Wiley & Sons

The depletion of volatile siderophile elements (VSE) Sn, Ag, Bi, Cd, and P in mantles of differentiated planetary bodies can be attributed to volatile‐depleted precursor materials (building blocks), fractionation during core formation, fractionation into and retention in sulfide minerals, and/or volatile loss associated with magmatism. Quantitative models to constrain the fractionation due to core formation have not been possible due to the lack of activity and partitioning data. Interaction parameters in Fe‐Si liquids have been measured at 1 GPa, 1600 °C and increase in the order Cd (~6), Ag (~10), Sn (~28), Bi (~46), and P (~58). These large and positive values contrast with smaller and negative values in Fe‐S liquids indicating that any chalcophile behavior exhibited by these elements will be erased by dissolution of a small amount of Si in the metallic liquid. A newly updated activity model is applied to Earth, Mars, and Vesta. Five elements (P, Zn, Sn, Cd, and In) in Earth’s primitive upper mantle can largely be explained by metal‐silicate equilibrium at high PT conditions where the core‐forming metal is a Fe‐Ni‐S‐Si‐C metallic liquid, but two other—Ag and Bi—become overabundant during core formation and require a removal mechanism such as late sulfide segregation. All of the VSE in the mantle of Mars are consistent with core formation in a volatile element depleted body, and do not require any additional processes. Only P and Ag in Vesta’s mantle are consistent with combined core formation and volatile‐depleted precursors, whereas the rest require accretion of chondritic or volatile‐bearing material after core formation. The concentrations of Zn, Ag, and Cd modeled for Vesta’s core are similar to the concentration range measured in magmatic iron meteorites indicating that these volatile elements were already depleted in Vesta’s precursor materials.

Carbonaceous matter in the Sariçiçek meteorite

1Mehmet Yesiltas,2Timothy D. Glotch,2Steven Jaret,3Alexander B. Verchovsky,3Richard C. Greenwood
Meteoritics & Planetary Science (in Press) Link to Article [https://doi.org/10.1111/maps.13287]
1Faculty of Aeronautics and Space Sciences, Kirklareli University, Kirklareli, 39100 Turkey
2Department of Geosciences, Stony Brook University, Stony Brook, New York, 11794 USA
3School of Physical Sciences, The Open University, Milton Keynes, MK7 6AA UK
Published by arrangement with John Wiley & Sons

As of today, the Sariçiçek (SC) meteorite is the newest howardite and the only confirmed fall among the 17 known howardites. In this study, we present isotopic, infrared, and Raman data on three distinct pieces of the SC meteorite. Our oxygen isotopic measurements show that Δ17O values of the pieces are close to each other, and are in good agreement with other howardites, eucrites, and diogenites. The carbon isotopic measurements, which were conducted by combusting terrestrial contamination selectively at temperatures lower than 500–600 °C, show the presence of indigenous carbon in the SC specimens. The matrix of these specimens, investigated via infrared microspectroscopy, appears to be dominated by clinopyroxene/orthopyroxene, forsterite, and fayalite, with minor contributions from ilmenite, plagioclase, and enstatite. Carbon‐rich regions were mapped and studied via Raman imaging microspectroscopy, which reveals that both amorphous and graphitic carbon exist in these samples. Synchrotron‐based infrared microspectroscopy data show the presence of very little aliphatic and aromatic hydrocarbons. The SC meteorite is suggested to be originating from the Antonia impact crater in the Rheasilvia impact basin on 4 Vesta (Unsalan et al. 2019). If this is in fact the case, then the carbon phases present in the SC samples might provide clues regarding the impactor material (e.g., carbonaceous chondrites).

Shock‐induced phase transformation of anorthitic plagioclase in the eucrite meteorite Northwest Africa 2650

1De‐Liang Chen,1,2Ai‐Cheng Zhang,1Run‐Lian Pang,1Jia‐Ni Chen,3Yang Li
Meteoritics & Planetary Science (in Press) Link to Article [https://doi.org/10.1111/maps.13286]
1State Key Laboratory for Mineral Deposits Research, School of Earth Sciences and Engineering, Nanjing University, Nanjing, 210023 China
2CAS Center for Excellence in Comparative Planetology, Hefei, 230026 China
3Institute of Geochemistry, Chinese Academy of Sciences, Guiyang, 550081 China
Published by arrangement with John Wiley & Sons

Anorthite is an important constituent mineral in basaltic achondrites from small celestial bodies. Its high‐pressure phase transformation in shocked meteorites has not been systematically studied. In this study, we report the diverse phase transformation behaviors of anorthite in a shocked eucrite Northwest Africa (NWA) 2650, which also contains coesite, stishovite, vacancy‐rich clinopyroxene, super‐silicic garnet, and reidite. Anorthite in NWA 2650 has transformed into anorthite glass (anorthite glassy vein, maskelynite, and glass with a schlieren texture and vesicles), tissintite and dissociated into three‐phase assemblage grossular + kyanite + silica glass. Different occurrences of anorthite glass might have formed via the mechanism involving shear melting, solid‐state transformation, and postshock thermally melting, respectively. Tissintite could have crystallized from a high‐pressure plagioclase melt. The nucleation of tissintite might be facilitated by relict pyroxene fragments and the early formed vacancy‐rich clinopyroxene. The three‐phase assemblage grossular, kyanite, and silica glass should have formed from anorthitic melt at high‐pressure and high‐temperature conditions. The presence of maskelynite and reidite probably suggests a minimum peak shock pressure up to 20 GPa, while the other high‐pressure phases indicate that the shock pressure during the crystallization of shock melt veins might vary from >8 GPa to >2 GPa with a heterogeneous temperature distribution.

Rethinking CO Antibiosignatures in the Search for Life Beyond the Solar System

Edward W. Schwieterman1,2,3,4, Christopher T. Reinhard3,5, Stephanie L. Olson3,6, Kazumi Ozaki3,5,7, Chester E. Harman3,8,9, Peng K. Hong10, and Timothy W. Lyons1,3
Astrophysical Journal 874, 9 Link to Article [DOI: 10.3847/1538-4357/ab05e1 ]
1Department of Earth Sciences, University of California, Riverside, CA, USA
2NASA Postdoctoral Program, Universities Space Research Association, Columbia, MD, USA
3NASA Astrobiology Institute, Alternative Earths & Virtual Planetary Laboratory Teams, USA
4Blue Marble Space Institute of Science, Seattle, WA, USA
5School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, GA, USA
6Department of Geophysical Sciences, University of Chicago, Chicago, IL, USA
7Department of Environmental Science, Toho University, Tokyo, Japan
8NASA Goddard Institute for Space Studies, New York, NY, USA
9Department of Applied Mathematics and Applied Physics, Columbia University, New York, NY, USA
10Planetary Exploration Research Center, Chiba Institute of Technology, 2-17-1 Tsudanuma, Narashino, Chiba 275-0016, Japan

Some atmospheric gases have been proposed as counter indicators to the presence of life on an exoplanet if remotely detectable at sufficient abundance (i.e., antibiosignatures), informing the search for biosignatures and potentially fingerprinting uninhabited habitats. However, the quantitative extent to which putative antibiosignatures could exist in the atmospheres of inhabited planets is not well understood. The most commonly referenced potential antibiosignature is CO, because it represents a source of free energy and reduced carbon that is readily exploited by life on Earth and is thus often assumed to accumulate only in the absence of life. Yet, biospheres actively produce CO through biomass burning, photooxidation processes, and release of gases that are photochemically converted into CO in the atmosphere. We demonstrate with a 1D ecosphere-atmosphere model that reducing biospheres can maintain CO levels of ~100 ppmv even at low H2 fluxes due to the impact of hybrid photosynthetic ecosystems. Additionally, we show that photochemistry around M dwarf stars is particularly favorable for the buildup of CO, with plausible concentrations for inhabited, oxygen-rich planets extending from hundreds of ppm to several percent. Since CH4 buildup is also favored on these worlds, and because O2 and O3 are likely not detectable with the James Webb Space Telescope, the presence of high CO (>100 ppmv) may discriminate between oxygen-rich and reducing biospheres with near-future transmission observations. These results suggest that spectroscopic detection of CO can be compatible with the presence of life and that a comprehensive contextual assessment is required to validate the significance of potential antibiosignatures.

The phase diagram of the Fe-P binary system at 3 GPa and implications for phosphorus in the lunar core

1,2Yuan Yin,1,2Zeming Li,1Shuangmeng Zhai
Geochimica et Cosmochimica Acta (in Press) Link to Article [https://doi.org/10.1016/j.gca.2019.03.037]
1Key Laboratory of High-temperature and High-pressure Study of the Earth’s Interior, Institute of Geochemistry, Chinese Academy of Sciences, Guiyang 550081, China
2University of Chinese Academy of Sciences, Beijing 100049, China
Copyright Elsevier

Phosphorus is a potential candidate in the metallic core of the Moon. The phase diagram of the Fe-P binary system was investigated at the pressure of 3 GPa and temperatures of up to 1600 °C. Up to 3.0 wt% and 10.4 wt% phosphorus can dissolve in the solid iron and liquid Fe-P phases at 1100 °C and 3 GPa, respectively. The eutectic temperature on the iron-rich side was determined as 1085 °C at 3 GPa. The solubility of phosphorus in the iron decreases from ∼1.4 wt% at 1100 °C to ∼0.7 wt% at 1500 °C and 3 GPa. Structure of the solid iron in the quenched sample is the body-center cubic, corresponding to α-Fe phase. Extending the phosphorus solubility in the solid iron to the present lunar core conditions yields a maximum phosphorus concentration in a fully crystallized iron core of 0.85 ± 0.15 wt%. If there are Ni and C in the core, the value would be depressed to 0.4 ± 0.1 wt%. In addition, based on a simple siderophile mass balance between the bulk Moon (BM) and bulk silicate Moon (BSM) and a modeled phosphorus partition coefficient, Dcore/mantle P-Moon(40 – 200) for the lunar magma ocean, a bulk silicate Earth-like P content (82 ± 8 ppm) in the initial Moon yields a lunar core with < 0.3 wt% P. Some other potential light elements such as S and C could reduce the P content in the lunar core. Furthermore, the partition coefficient of phosphorus in the iron and liquid melt (DSM/LM P) was found to be 0.10 ± 0.03 at 3 GPa. Taking the sulfur into account, the DSM/LM P increase to 0.18 ± 0.02 at 5 GPa in the S-rich liquid metal (∼8 wt%). In the case of a solid lunar inner core and S-bearing liquid outer core, their P contents were assessed to be less than 0.09 ± 0.01 wt% and 0.51 ± 0.01 wt%, respectively, when the lunar core’s storage of P is <0.3 wt%. The moderate phosphorus solubility in the solid iron, combined with the assumption of abundant phosphorus in the bulk Moon, indicates that the phosphorus concentration in the lunar core could higher than previously thought.

A High-resolution Mid-infrared Survey of Water Emission from Protoplanetary Disks

Colette Salyk1, John Lacy2, Matt Richter3, Ke Zhang4, Klaus Pontoppidan5, John S. Carr6, Joan R. Najita7, and Geoffrey A. Blake8
Astrophysical Journal 874, 24 Link to Article [DOI: 10.3847/1538-4357/ab05c3 ]
1Department of Physics and Astronomy, Vassar College, 124 Raymond Avenue, Poughkeepsie, NY 12604, USA
2Department of Astronomy, University of Texas at Austin, Austin, TX 78712, USA
3Physics Department, University of California at Davis, Davis, CA 95616, USA
4Department of Astronomy, University of Michigan, 311 West Hall, 1085 South University Avenue, Ann Arbor, MI 48109, USA
5Space Telescope Science Institute, 3700 San Martin Drive, Baltimore, MD 21218, USA
6Naval Research Laboratory, Code 7213, Washington, DC 20375, USA
7National Optical Astronomy Observatory, 950 N. Cherry Avenue, Tucson, AZ 85719, USA
8Division of Geological and Planetary Sciences, California Institute of Technology, MC 150-21, 1200 E California Boulevard, Pasadena, CA 91125, USA

We present the largest survey of spectrally resolved mid-infrared water emission to date, with spectra for 11 disks obtained with the Michelle and TEXES spectrographs on Gemini North. Water emission is detected in six of eight disks around classical T Tauri stars. Water emission is not detected in the transitional disks SR 24 N and SR 24 S, in spite of SR 24 S having pretransitional disk properties like DoAr 44, which does show water emission. With R ~ 100,000, the TEXES water spectra have the highest spectral resolution possible at this time, and allow for detailed line shape analysis. We find that the mid-IR water emission lines are similar to the “narrow component” in CO rovibrational emission, consistent with disk radii of a few astronomical units. The emission lines are either single peaked, or consistent with a double peak. Single-peaked emission lines cannot be produced with a Keplerian disk model, and may suggest that water participates in the disk winds proposed to explain single-peaked CO emission lines. Double-peaked emission lines can be used to determine the radius at which the line emission luminosity drops off. For HL Tau, the lower limit on this measured dropoff radius is consistent with the 13 au dark ring. We also report variable line/continuum ratios from the disks around DR Tau and RW Aur, which we attribute to continuum changes and line flux changes, respectively. The reduction in RW Aur line flux corresponds with an observed dimming at visible wavelengths.