^1,2Renyu Hu
Earth and Planetary Science Letters 519, 192-201 Link to Article [https://doi.org/10.1016/j.epsl.2019.05.017]
¹Jet Propulsion Laboratory, California Institute of Technology, Pasadena, CA 91109, USA
²Division of Planetary and Geological Science, California Institute of Technology, Pasadena, CA 91125, USA
Copyright Elsevier

Regolith on Mars exchanges water with the atmosphere on a diurnal basis and this process causes significant variation in the abundance of water vapor at the surface. While previous studies of regolith-atmosphere exchange focus on the abundance, recent in-situ experiments and remote sensing observations measure the isotopic composition of the atmospheric water. We are therefore motivated to investigate isotopic water exchange between the atmosphere and the regolith and determine its effect on the deuterium to hydrogen ratio (D/H) of the atmosphere. We model transport of water in the regolith and regolith-atmosphere exchange by solving a transport equation including regolith adsorption, condensation, and diffusion. The model calculates equilibrium fractionation between HDO and H2O in each of these processes. The fractionation in adsorption is caused by the difference in the latent heat of adsorption, and that of condensation is caused by the difference in the vapor pressure. Together with a simple, bulk-aerodynamic boundary layer model, we simulate the diurnal variation of the D/H near the planetary surface. We find that the D/H can vary by 300–1400‰ diurnally in the equatorial and mid-latitude locations, and the magnitude is greater at a colder location or season. The variability is mainly driven by adsorption and desorption of regolith particles, and its diurnal trend features a drop in the early morning, a rise to the peak value during the daytime, and a second drop in the late afternoon and evening, tracing the water vapor flow into and out from the regolith. The predicted D/H variation can be tested with in-situ measurements. As such, our calculations suggest stable isotope analysis to be a powerful tool in pinpointing regolith-atmosphere exchange of water on Mars.

¹A.Néri,¹J.Guignard,¹M.Monnereau,¹M.J.Toplis,¹G.Quitté
Earth and Planetary Science Letters 518, 40-52 Link to Article [https://doi.org/10.1016/j.epsl.2019.04.049]
¹IRAP, Université de Toulouse, CNRS, CNES, UPS, Toulouse, France
Copyright Elsevier

High temperature experiments have been performed to constrain interfacial energies in a three-phase system (metal–forsterite–silicate melt) representative of partially differentiated planetesimals accreted early in the solar system history, with the aim of providing new insights into the factors affecting the interconnection threshold of metal-rich phases. Experiments were run under controlled oxygen fugacity (ΔNi-NiO=−3) at 1440 °C, typically for 24 h. Quantification of the true dihedral angles requires a resolution of at least 30 nm per pixel in order to reveal small-angle wedges of silicate melt at crystal interfaces. At this level of resolution, dihedral angle distributions of silicate melt and olivine appear asymmetric, an observation interpreted in terms of anisotropy of olivine crystals. Based upon the theoretical relation between dihedral angles and interfacial energies in a three-phase system, the relative magnitudes of interfacial energies have been determined to be: γMelt-Ol<γMelt-Ni<γOl-Ni. This order differs from that obtained with experiments using an iron sulfide liquid close to the Fe–FeS eutectic for which γMelt-Sulfide<γMelt-Ol<γOl-Sulfide, implying a lower interconnection threshold for sulfur-rich melts than for pure metallic phases. This dependence of the interconnection threshold on the sulfur content will affect the drainage of metallic phases during melting of small bodies. Assuming a continuous extraction of silicate melt, evolution of the metal volume fraction has been modeled. Several sulfur-rich melts extraction events are possible over a range of temperatures relevant with thermometric data on primitive achondrites (1200–1400 °C and 25% of silicate melt extracted). These successive events provide novel insight into the variability of sulfur content in primitive achondrites, which are either representative of a region that experienced sulfide extraction or from a region that accumulated sulfide melt from overlying parts of the parent body.

Yasuhiro Hasegawa¹, Bradley M. S. Hansen², and Gautam Vasisht¹
Astrophysical Journal Letters 876, L32 Link to Article [DOI: 10.3847/2041-8213/ab1b5a]
¹Jet Propulsion Laboratory, California Institute of Technology, Pasadena, CA 91109, USA
²Mani L. Bhaumik Institute for Theoretical Physics, Department of Physics & Astronomy, University of California Los Angeles, Los Angeles, CA 90095, USA

Identification of the main planet formation site is fundamental to understanding how planets form and migrate to their current locations. We consider the heavy-element content trend of observed exoplanets, derived from improved measurements of mass and radius, and explore how this trend can be used as a tracer of their formation sites. Using gas accretion recipes obtained from hydrodynamical simulations, we confirm that the disk-limited gas accretion regime is most important for reproducing the trend. Given that such a regime is specified by two characteristic masses of planets, we compute these masses as a function of the distance (r) from the central star, and then examine how the regime appears in the mass–semimajor axis diagram. Our results show that a plausible solid accretion region emerges at r  0.6 au and expands with increasing r, using the conventional disk model. Given that exoplanets that possess the heavy-element content trend distribute currently near their central stars, our results imply the importance of planetary migration that would occur after solid accretion onto planets might be nearly completed at r ≥ 0.6 au. Self-consistent simulations would be needed to verify the predictions herein.

¹Robert M. Hazen
American Mineralogist 104, 810-816 Link to Article [http://www.minsocam.org/MSA/AmMin/TOC/2019/open_access/AM104P0810.pdf]
¹Geophysical Laboratory, Carnegie Institution for Science, 5251 Broad Branch Road NW, Washington, D.C. 20015, U.S.A. Orcid: 0000-0003-4163-8644
Copyright: The Mineralogical Society of America

Minerals reveal the nature of the co-evolving geosphere and biosphere through billions of years of Earth history. Mineral classification systems have the potential to elucidate this rich evolutionary story; however, the present mineral taxonomy, based as it is on idealized major element chemistry and crystal structure, lacks a temporal aspect, and thus cannot reflect planetary evolution. A complementary evolutionary system of mineralogy based on the quantitative recognition of “natural kind clustering” for a wide range of condensed planetary materials with different paragenetic origins has the potential to amplify, though not supersede, the present classification system.