Capturing the oxidation of silicon carbide in rocky exoplanetary interiors

Theoretical models predict the condensation of silicon carbide around host stars with C/O ratios higher than 0.65 (cf. C/O$_{\mathrm{Sun}}$ = 0.54), in addition to its observations in meteorites, interstellar medium and protoplanetary disks. Consequently, the interiors of rocky exoplanets born from carbon-enriched refractory material are often assumed to contain large amounts of silicon carbide. Here we aim to investigate the stability of silicon carbide in the interior of carbon-enriched rocky exoplanets and to derive the reaction leading to its transformation. We performed a high-pressure high-temperature experiment to investigate the reaction between a silicon carbide layer and a layer representative of the bulk composition of a carbon-enriched rocky exoplanet. We report the reaction leading to oxidation of silicon carbide producing quartz, graphite, and molten iron silicide. Combined with previous studies, we show that in order to stabilize silicon carbide, carbon saturation is not sufficient, and a complete reduction of Fe$^{2+}$ to Fe$^{0}$ in a planetary mantle is required, suggesting that future spectroscopic detection of Fe$^{2+}$ or Fe$^{3+}$ on the surface of rocky exoplanets would imply the absence of silicon carbide in their interiors.Comment: Accepted for publication in Astronomy & Astrophysic

In situ Viscometry of Primitive Lunar Magmas at High Pressure and High Temperature

Understanding the dynamics of the magmatic evolution of the interior of the Moon requires accurate knowledge of the viscosity (η) of lunar magmas at high pressure (P) and high temperature (T) conditions. Although the viscosities of terrestrial magmas are relatively well-documented, and their relation to magma composition well-studied, the viscosities of lunar titano-silicate melts are not well-known. Here, we present an experimentally measured viscosity dataset for three end member compositions, characterized by a wide range of titanium contents, at lunar-relevant pressure-temperature range of ∼1.1–2.4 GPa and 1830–2090 K. In situ viscometry using the falling sphere technique shows that the viscosity of lunar melts varies between ∼0.13 and 0.87 Pa-s depending on temperature, pressure and composition. Viscosity decreases with increasing temperature with activation energies for viscous flow of Ea = 201 kJ/mol and Ea = 106 kJ/mol for low-titanium (Ti) and high-Ti melts, respectively. Pressure is found to mildly increase the viscosity of these intermediate polymerized melts by a factor of ∼1.5 between 1.1 and 2.4 GPa. Viscosities of low-Ti and high-Ti magmas at their respective melting temperatures are very close. However at identical P-T conditions (∼1.3 GPa, ∼1840 K) low-Ti magmas are about a factor of three more viscous than high-Ti magmas, reflecting structural effects of Si and Ti on melt viscosity. Measured viscosities differ significantly from empirical models based on measurements of the viscosity of terrestrial basalts, with largest deviations observed for the most Ti-rich and Si-poor composition. Viscosity coefficients for these primitive lunar melts are found to be lower than those of common terrestrial basalts, giving them a high mobility throughout the lunar mantle and onto the surface of the Moon despite their Fe and Ti-rich compositions

Experimental and computational study of trace element distribution between orthopyroxene and anhydrous silicate melts: substitution mechanisms and the effect of iron

Although orthopyroxene (Opx) is present during a wide range of magmatic differentiation processes in the terrestrial and lunar mantle, its effect on melt trace element contents is not well quantified. We present results of a combined experimental and computational study of trace element partitioning between Opx and anhydrous silicate melts. Experiments were performed in air at atmospheric pressure and temperatures ranging from 1,326 to 1,420°C in the system CaO-MgO-A

Quantifying garnet-melt trace element partitioning using lattice-strain theory: New crystal-chemical and thermodynamic constraints

Many geochemical models of major igneous differentiation events on the Earth, the Moon, and Mars invoke the presence of garnet or its high-pressure majoritic equivalent as a residual phase, based on its ability to fractionate critical trace element pairs (Lu/Hf, U/Th, heavy REE/light REE). As a result, quantitative descriptions of mid-ocean ridge and hot spot magmatism, and lunar, martian, and terrestrial magma oceans require knowledge of garnet-melt partition coefficients over a wide range of conditions. In this contribution, we present new crystal-chemical and thermodynamic constraints on the partitioning of rare earth elements (REE), Y and Sc between garnet and anhydrous silicate melt as a function of pressure (P), temperature (T), and composition (X). Our approach is based on the interpretation of experimentally determined values of partition coefficients D using lattice-strain theory. In this and a companion paper (Draper and van Westrenen this issue) we derive new predictive equations for the ideal ionic radius of the dodecahedral garnet X-site,

Solar System Exploration Research Virtual Institute: Year Three Annual Report 2016

NASA's Solar System Exploration Research Virtual Institute (SSERVI) is pleased to present the 2016 Annual Report. Each year brings new scientific discoveries, technological breakthroughs, and collaborations. The integration of basic research and development, industry and academic partnerships, plus the leveraging of existing technologies, has further opened a scientific window into human exploration. SSERVI sponsorship by the NASA Science Mission Directorate (SMD) and Human Exploration and Operations Mission Directorate (HEOMD) continues to enable the exchange of insights between the human exploration and space science communities, paving a clearer path for future space exploration. SSERVI provides a unique environment for scientists and engineers to interact within multidisciplinary research teams. As a virtual institute, the best teaming arrangements can be made irrespective of the geographical location of individuals or laboratory facilities. The interdisciplinary science that ensues from virtual and in-person interactions, both within the teams and across team lines, provides answers to questions that many times cannot be foreseen. Much of this research would not be accomplished except for the catalyzing, collaborative environment enabled by SSERVI. The SSERVI Central Office, located at NASA Ames Research Center in Silicon Valley, California, provides the leadership, guidance and technical support that steers the virtual institute. At the start of 2016, our institute had nine U.S. teams, each mid-way through their five-year funding cycle, plus nine international partnerships. However, by the end of the year we were well into the selection of four new domestic teams, selected through NASA's Cooperative Agreement Notice (CAN) process, and a new international partnership. Understanding that human and robotic exploration is most successful as an international endeavor, international partnerships collaborate with SSERVI domestic teams on a no-exchange of funds basis, but they bring a richness to the institute that is priceless. The international partner teams interact with the domestic teams in a number of ways, including sharing students, scientific insights, and access to facilities. We are proud to introduce our newest partnership with the Astrophysics and Planetology Research Institute (IRAP) in Toulouse, France. In 2016, Principal Investigator Dr. Patrick Pinet assembled a group of French researchers who will contribute scientific and technological expertise related to SSERVI research. SSERVI's domestic teams compete for five-year funding opportunities through proposals to a NASA CAN every few years. Having overlapping proposal selection cycles allows SSERVI to be more responsive to any change in direction NASA might experience, while providing operational continuity for the institute. Allowing new teams to blend with the more seasoned teams preserves corporate memory and expands the realm of collaborative possibilities. A key component of SSERVI's mission is to grow and maintain an integrated research community focused on questions related to the Moon, Near-Earth asteroids, and the moons of Mars. The strong community response to CAN-2 demonstrated the health of that effort. NASA Headquarters conducted the peer-review of 22 proposals early in 2017 and, based on recommendations from the SSERVI Central Office and NASA SSERVI program officers, the NASA selecting officials determined the new teams in the spring of 2017. We are pleased to welcome the CAN-2 teams into the institute, and look forward to the collaborations that will develop with the current teams. The new teams are: The Network for Exploration and Space Science (NESS) team (Principal Investigator (PI) Prof. Jack Burns/U. Colorado); the Exploration Science Pathfinder Research for Enhancing Solar System Observations (ESPRESSO) team (PI Dr. Alex Parker/Southwest Research Institute); the Toolbox for Research and Exploration (TREX) team (PI Dr. Amanda Hendrix/ Planetary Science Institute); and the Radiation Effects on Volatiles and Exploration of Asteroids & Lunar Surfaces (REVEALS) team (PI Prof. Thomas Orlando/ Georgia Institute of Technology). In this report, you will find an overview of the 2016 leadership activities of the SSERVI Central Office, reports prepared by the U.S. teams from CAN-1, and achievements from several of the SSERVI international partners. Reflecting on the past year's discoveries and advancements serves as a potent reminder that there is still a great deal to learn about NASA's target destinations. Innovation in the way we access, sample, measure, visualize, and assess our target destinations is needed for further discovery. At the same time, let us celebrate how far we have come, and strongly encourage a new generation that will make the most of future opportunities

Toxicity of lunar dust

The formation, composition and physical properties of lunar dust are incompletely characterised with regard to human health. While the physical and chemical determinants of dust toxicity for materials such as asbestos, quartz, volcanic ashes and urban particulate matter have been the focus of substantial research efforts, lunar dust properties, and therefore lunar dust toxicity may differ substantially. In this contribution, past and ongoing work on dust toxicity is reviewed, and major knowledge gaps that prevent an accurate assessment of lunar dust toxicity are identified. Finally, a range of studies using ground-based, low-gravity, and in situ measurements is recommended to address the identified knowledge gaps. Because none of the curated lunar samples exist in a pristine state that preserves the surface reactive chemical aspects thought to be present on the lunar surface, studies using this material carry with them considerable uncertainty in terms of fidelity. As a consequence, in situ data on lunar dust properties will be required to provide ground truth for ground-based studies quantifying the toxicity of dust exposure and the associated health risks during future manned lunar missions.Comment: 62 pages, 9 figures, 2 tables, accepted for publication in Planetary and Space Scienc

Constraints on early Earth's water budget from the evolution of the lunar hydrogen cycle

During the Hadean, Earth recovered from the Moon-forming giant impact, became covered with liquid water oceans, and witnessed the onset of plate tectonics and life. Quantifying the abundances, distribution, and chemical states of water in the atmosphere, on the surface, and in the interior of the early Earth is essential to constrain the early evolution of System Earth. Assessing these parameters is hampered by the general dearth of early Earth samples, the difficulty of distinguishing primary signatures from later alteration processes in such samples, leading to large uncertainties on the influx and outflux of water to and from the early Earth. Given the close proximity of Earth and Moon, constraints on the early hydrogen cycle in the Moon may reflect coeval aspects of the water cycle on early Earth. Here, we assess constraints on the lunar water cycle from the time the Moon formed until the end of late accretion at ~3.8 Ga, and implications of these constraints for the early Earth water budget. Dynamic accretion models suggest the Moon initially contained ~455 ppm of water. Recent experimental studies of lunar magma ocean crystallization suggest similarly substantial initial lunar water contents. Hydrogen concentration measurements in lunar plagioclase crystals derived from the magma ocean illustrate that the Moon experienced significant degassing during the solidification of the lunar magma ocean (thought to have occurred between 4.5 and ~ 4.3 Ga). Hydrogen and chlorine systematics in lunar magmatic apatite grains formed between ~4.1 Ga and ~ 3 Ga indicate that lunar hydrogen reservoirs were replenished by volatile delivery during late accretion (~4.1–3.8 Ga), after which the water abundance of the Moon stabilized. Using this knowledge of the lunar water cycle to model Earth's early water budget leads to two scenarios that are consistent with the observed present-day terrestrial water content of 1000–3000 ppm: (1) Earth contained significantly more water than the Moon-forming material immediately after the giant impact, suggesting hydrogen heterogeneity in the initial Earth-Moon system; (2) Earth did not experience significant degassing in the aftermath of the giant impact, and the late accretion mass added to Earth was large and water-ric

Isotopic evidence for volatile replenishment of the Moon during the Late Accretion

The traditional view of a dry, volatile-poor Moon has been challenged by the identification of water and other volatiles in lunar samples, but the volatile budget delivery time(s), source(s) and temporal evolution remain poorly constrained. Here we show that hydrogen and chlorine isotopic ratios in lunar apatite changed significantly during the Late Accretion (LA, 4.1-3.8 billion years ago). During this period, deuterium/hydrogen ratios in the Moon changed from initial carbonaceous-chondrite-like values to values consistent with an influx of ordinary-chondrite-like material and pre-LA elevated δ37Cl values drop towards lower chondrite-like values. Inferred pre-LA lunar interior water contents are significantly lower than pristine values suggesting degassing, followed by an increase during the LA. These trends are consistent with dynamic models of solar-system evolution, suggesting that the Moon's (and Earth's) initial volatiles were replenished ∼0.5 Ga after their formation, with their final budgets reflecting a mixture of sources and delivery times