Observations of alkaline emissions NaI, KI and LiI during first minutes after DART probe impact on Dimorphos

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¹L. Shestakova,¹A. Serebryanskiy,¹G. Aimanova
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2023.115595]
¹Fesenkov Astrophysical Institute, Obseravtory, 23, Almaty, 050020, Kazakhstan
Copyright Elsevier

We report on the results of the analysis of spectral observations of the asteroid Didymos at the time of impact of the DART mission probe, obtained a few minutes before, directly at the moment, and within a few minutes after the spacecraft hit the surface of the Dimorphos. We found evidence of alkali metal emissions that appeared at the moment and continued for several minutes after the impact. The observation evidence of the appearance of Na, Li and K atoms as a result of the impact of the DART probe on the Dimorphos in a relative amount close to the abundance of these elements in the Solar System are reliably established. We conclude that the main contribution to alkaline emissions is atoms bound to the dust cloud ejected during the impact. This dust cloud is a steady source of alkaline metal atoms. We did not detect the presence of alkaline mater not bound to the dust cloud and moved independently.

Boron adsorption in clay minerals: Implications for martian groundwater chemistry and boron on Mars

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¹Matthew A. Nellessen et al. (>10)
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2023.115599]
¹Earth and Planetary Sciences, University of New Mexico, Albuquerque, NM, USA
Copyright Elsevier

Boron has been detected on Mars in calcium-sulfate veins found within clay mineral rich rocks on Mars by the Mars Science Laboratory (MSL) Curiosity rover using Laser Induced Breakdown Spectroscopy (LIBS) analysis. Borates play a vital role in stabilizing ribose on Earth and has been suggested as a key requirement for life. Borate ions readily adsorb to phyllosilicate clay minerals. The discovery of boron on Mars in proximity to phyllosilicate-bearing bedrock may have strong implications for potential past prebiotic conditions on Mars. In this study we generated a suite of clay minerals with adsorbed borate, including both typical terrestrial clay minerals (montmorillonite) and Mars-analog clay minerals (nontronite, saponite, griffithite), to understand controls on borate adsorption and to analyze with LIBS to compare with MSL data. Clay minerals were subjected to mineralogical and chemical analysis before and after adsorption. Adsorption analysis revealed that the Mars analog clay minerals adsorbed less boron than terrestrial counterparts, but within comparable amounts to those detected on Mars and in meteorites. Post-adsorption analysis by X-ray diffraction (XRD) revealed slight changes in the interlayer spacing of many of the clay minerals. Based on the adsorption analysis of the Mars-analog clay minerals, phyllosilicate-bearing bedrock in Gale crater may contain up to 90-110 ppm B. A series of borate-enriched samples were created for analysis of LIBS spectra from ChemCam on the Curiosity rover and SuperCam on the Perseverance Rover. The results of this study may provide insight into martian groundwater geochemistry processes and the mobility of a key molecule connected with life.

Visible to near-infrared reflectance and Raman spectra of evaporites from sulfate-chloride Mars analogue brines

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^1,2Emmy B. Hughes,¹Martha Gilmore,³Peter E. Martin,⁴Miriam Eleazer
Icarus (in Press) Link to Article [https://doi.org/10.1016/j.icarus.2023.115597]
¹Department of Earth and Environmental Sciences, Wesleyan University, 265 Church St., Middletown, CT 06438, United States of America
²School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, GA, United States of America
³Department of Geological Sciences, University of Colorado, Boulder
⁴Department of Astronomy, Wesleyan University, Middletown, CT, United States of America
Copyright Elsevier

While much attention has been given to the identification and characterization of single-phase salts on Mars, relatively little has been applied to mixed evaporative assemblages. Given the likely existence of these assemblages on Mars (e.g., basin deposits) and the lack of data on their spectral signatures, here we present an experimental study of multicomponent S and Cl-bearing Mars-relevant brines. We modeled, synthesized and evaporated brines in the laboratory under both martian and terrestrial (P, T, pCO2) environmental conditions, and characterized the resulting precipitates using Visible–Near Infrared (VNIR), Raman spectroscopy, XRD and SEM-EDS. We compared these results to mineral assemblages calculated using the FREZCHEM thermodynamic model. For mixed brines primarily containing Na+, K+, Mg2+, Ca2+, SO42− and Cl−, epsomite (MgSO4•7H2O) and bischofite (MgCl2•6H2O) overwhelm VNIR and Raman spectra, while anhydrous crystalline salts and Na- and K-sulfates are unidentified. Mg-sulfates are identifiable in the VNIR and Raman even at low or no modeled mass abundance in an evaporative assemblage and are often the only clearly identifiable salt. These results imply that regions of Mg-sulfate identification on Mars may have only minor amounts of Mg-sulfate present, and significant amounts of halides or other sulfates may be undetectable. This may be due to a combination of late-stage Mg-sulfate precipitation and non-linear spectral mixing. Raman is more sensitive than VNIR to the identification of Ca-sulfate salts in these mixed assemblages. We predict that high abundances of mixed chloride and sulfate salts species will be identified as the Curiosity Rover continues to explore the Sulfate Unit of Gale Crater, and note that the Perseverance rover offers the first opportunity to identify such mixed assemblages in Jezero Crater with this combination of techniques.

Carbon-rich icy moons and dwarf planets

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¹Bruno Reynard,²Christophe Sotin
Earth and Planetary Science Letters 612, 118172 Link to Article [https://doi.org/10.1016/j.epsl.2023.118172]
¹Univ Lyon, ENS Lyon, UCB Lyon 1, Univ St-Etienne, CNRS, Laboratoire de Géologie de Lyon, 69007 Lyon, France
²Laboratoire de Planétologie et Géosciences, Nantes Université, Univ Angers, Le Mans Université, CNRS, UMR 6112, F-44000 Nantes, France
Copyright Elsevier

Density and moment of inertia of icy moons and dwarf planets suggest the presence of a low-density carbonaceous component in their rocky cores. This hypothesis was tested using inner density structure and thermal models. Rocky core densities in dwarf planets and icy moons are found to consist of a mixture of chondritic silicate-sulfide rocks and carbonaceous matter. Carbonaceous matter was originally mixed with ice in a rock-free precursor. In a homogeneous accretion scenario where these components are mixed in solar proportions, ices then differentiated from the carbon-rich refractory core, while hydration of silicates could take place. Thermal models taking into account the presence of carbonaceous matter suggest that originally hydrated silicates are only partially dehydrated in the refractory cores of most moons. Viable scenarios point to a difference in formation or evolution between Ganymede and Titan in spite of their similar size and mass. Fully dehydrated mineralogies, inferred in Europa and possibly the densest dwarf planet Eris, require heterogeneous accretion near the water snow line of the solar or circumplanetary nebula. Progressive gas release from slowly warming carbonaceous matter-rich cores may sustain up to present-day the replenishment of ice-oceanic layers in organics and volatiles. It accounts for the observation of nitrogen, light hydrocarbons and complex organic molecules at the surface, in the atmospheres, or in plumes emanating from moons and dwarf planets. The formation of large carbon-rich bodies in the outer solar system suggests that carbon-rich planets could form at the outskirts of extrasolar systems.

The breakdown of diopside to (Ca, Mg)SiO3 perovskite–(Mg, Ca, Fe)SiO3 glass–(Mg, Ca)SiO3 glass–(Mg, Ca)SiO3 majorite in a melt vein the Suizhou L6 chondrite

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¹Xie, Xiande,²Gu, Xiangping
Acta Geochimica 42, 183 – 194 Link to Article [DOI 10.1007/s11631-023-00594-x]
¹Key Laboratory of Mineralogy and Metallogeny / Guangdong Provincial Key Laboratory of Mineral Physics and Materials, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, 510640, China
²School of Geosciences and Info-Physics, Central South University, Changsha, 410083, China