^1,2M.D.Suttle,^2,3L.Folco,^2,4M.J.Genge,¹S.S.Russell
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2020.113956]
¹Planetary Materials Group, Department of Earth Sciences, Natural History Museum, Cromwell Road, London SW7 5BD, UK
²Dipartimento di Scienze della Terra, Università di Pisa, 56126 Pisa, Italy
³CISUP, Centro per l’Integrazione della Strumentazione dell’Università di Pisa, Lungarno Pacinotti 43, 56126 Pisa, Italy
⁴Impacts and Astromaterials Research Centre, Department of Earth Science and Engineering, Imperial College London, South Kensington, London SW7 2AZ, UK
Copyright Elsevier

Comets are typically considered to be pristine remnants of the early solar system. However, by definition they evolve significantly over their lifetimes through evaporation, sublimation, degassing and dust release. This occurs once they enter the inner solar system and are heated by the Sun. Some comets (e.g. 1P/Halley, 9P/Tempel and Hale-Bopp) as well as chondritic porous cosmic dust – released from comets – show evidence of minor aqueous alteration resulting in the formation of phyllosilicates, carbonates or other secondary phases (e.g. Cu-sulphides, amphibole and magnetite). These observations suggest that (at least some) comets experienced limited interaction with liquid water under conditions distinct from the alteration histories of hydrated chondritic asteroids (e.g. the CM and CR chondrites).

This synthesis paper explores the viability of perihelion-induced heating as a mechanism for the generation of highly localised subsurface liquid water and thus mild aqueous alteration in periodic comets. We draw constraints from experimental laboratory studies, numerical modelling, spacecraft observations and microanalysis studies of cometary micrometeorites. Both temperature and pressure conditions necessary for the generation and short-term (hour-long) survival of liquid water are plausible within the immediate subsurface (<0.5 m depth) of periodic comets with small perihelia (<1.5 A.U.), low surface permeabilities and favourable rotational states (e.g. high obliquities and/or slow rotational periods). We estimate that solar radiant heating may generate liquid water and perform aqueous alteration reactions in 3–9% of periodic comets. An example of an ideal candidate is 2P/Encke which has a small perihelion (0.33 A.U.), a high obliquity and a short orbital period. This comet should therefore be considered a high priority candidate in future spectroscopic studies of comet surfaces. Small quantities of phyllosilicate generated by aqueous alteration may be important in cementing together grains in the subsurface of older dormant comets, thereby explaining observations of unexpectedly high tensile strength in some bodies.

Most periodic comets which currently pass close to the Sun are dormant, having experienced surface heating, significant cometary activity and dust release in the past. These bodies may be responsible for the partially hydrated cometary micrometeorites we find at the Earth’s surface and their aqueous alteration histories may have been produced by perihelion-induced subsurface heating. This is in contrast to radiogenic and impact heating that operated during the early solar system on asteroids. This study has implications for the alteration history of the active asteroid Phaethon, the target of JAXA’s DESTINY+ mission.

¹J.V.Clark,²P.D.Archer,³J.E.Gruener,³D.W.Ming,²V.M.Tu,³P.B.Niles,⁴S.A.Mertzman
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2020.113936]
¹GeoControls Systems, Inc – Jacobs JETS Contract at NASA Johnson Space Center, 2101 NASA Pkwy, Houston, TX 77058, USA
²Jacobs JETS Contract at NASA Johnson Space Center, 2101 NASA Pkwy, Houston, TX 77058, USA
³NASA Johnson Space Center, 2101 NASA Pkwy, Houston, TX 77058, USA
⁴Department of Earth and Environmental, Franklin & Marshall College, Lancaster, PA 17604, USA
Copyright Elsevier

The Johnson Space Center-Rocknest (JSC-RN) simulant was developed in response to a need by NASA’s Advanced Exploration Systems (AES) In-Situ Resource Utilization (ISRU) project for a simulant to be used in component and system testing for water extraction from Mars regolith. JSC-RN was designed to be chemically and mineralogically similar to material from the aeolian sand shadow named Rocknest in Gale Crater, particularly the 1–3 wt% low temperature (<450 °C) water release as measured by the Sample Analysis at Mars (SAM) instrument on the Curiosity rover. Sodium perchlorate, goethite, pyrite, ferric sulfate, regular and high capacity granular ferric oxide, and forsterite were added to a Mojave Mars Simulant (MMS) base in order to match the mineralogy, evolved gases, and elemental chemistry of Rocknest. Mineral and rock components were sent to the United States Geological Survey (USGS) in Denver for mixing. Approximately 800 kg of JSC-RN was sent back to NASA in 5 gal buckets, which were subsampled and characterized. All samples of the USGS-produced simulants had similar evolved gas profiles as a small prototype batch of JSC-RN made in JSC laboratories, with the exception of HCl, and were similar in terms of mineralogy and total chemistry. Also, all JSC-RN subsamples were homogenous and had similar mineralogy, total chemistry, and low-temperature evolved gas profiles as the Rocknest aeolian sand shadow examined with Curiosity‘s instrument suite on Mars. In particular, the low temperature water releases were similar and the amount of water evolved from JSC-RN at <450 °C was similar to the water content of Rocknest based on SAM water peak integrations. Overall, JSC-RN is ideally suited for ISRU studies of water extraction of global martian soil due to its excellent agreement with measured properties of martian soils and its proven feasibility for large-scale production.

¹Adrian Brearley
Meteoritics & Planetary Science (in Press) Link to Article [https://doi.org/10.1111/maps.13537]
¹Department of Earth and Planetary Sciences, University of New Mexico, Albuquerque, New Mexico, 87131 USA
Published by arrangement with John Wiley & Sons

Transmission electron microscope studies of fine‐grained rims in three CM2 carbonaceous chondrites, Y‐791198, Murchison, and ALH 81002, have revealed the presence of widespread nanoparticles with a distinctive core–shell structure, invariably associated with carbonaceous material. These nanoparticles vary in size from ~20 nm up to 50 nm in diameter and consist of a core of Fe,Ni carbide surrounded by a continuous layer of polycrystalline magnetite. These magnetite shells are 5–7 nm in thickness irrespective of the diameter of the core Fe,Ni carbide grains. A narrow layer of amorphous carbon a few nanometers in thickness is present separating the carbide core from the magnetite shell in all the nanoparticles observed. The Fe,Ni carbide phases that constitute the core are consistent with both haxonite and cohenite, based on electron diffraction data, energy dispersive X‐ray analysis, and electron energy loss spectroscopy. Z‐contrast scanning transmission electron microscopy shows that these core–shell magnetite‐carbide nanoparticles can occur as individual isolated grains, but more commonly occur in clusters of multiple particles. In addition, energy‐filtered transmission electron microscopy (EFTEM) images show that in all cases, the nanoparticles are embedded within regions of carbonaceous material or are coated with carbonaceous material. The observed nanostructures of the carbides and their association with carbonaceous material can be interpreted as being indicative of Fischer–Tropsch‐type (FTT) reactions catalyzed by nanophase Fe,Ni metal grains that were carburized during the catalysis reaction. The most likely environment for these FTT reactions appears to be the solar nebula consistent with the high thermal stability of haxonite and cohenite, compared with other carbides and the evidence of localized catalytic graphitization of the carbonaceous material. However, the possibility that such reactions occurred within the CM parent body cannot be excluded, although this scenario seems unlikely, because the kinetics of the reaction would be extremely slow at the temperatures inferred for CM asteroidal parent bodies. In addition, carbides are unlikely to be stable under the oxidizing conditions of alteration experienced by CM chondrites. Instead, it is most probable that the magnetite rims on all the carbide particles are the product of parent body oxidation of Fe,Ni carbides, but this oxidation was incomplete, because of the buildup of an impermeable layer of amorphous carbon at the interface between the magnetite and the carbide phase that arrested the reaction before it went to completion. These observations suggest that although FTT catalysis reactions may not have been the major mechanism of organic material formation within the solar nebula, they nevertheless contributed to the inventory of complex insoluble organic matter that is present in carbonaceous chondrites.