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The cameras on the Pathfinder probe (Imager for Pathfinder) and the rovers Spirit and Opportunity (Panoramic Camera), Curiosity (Mast Camera) and Perseverance (Mast Camera-Z) produce visible-range spectra of limited wavelength resolution but of great target resolution which allows mineralogical analysis of selected areas within martian rocks. Laboratory spectra of relevant specimens were transformed into the spectra corresponding to each of the above cameras to increase our capability to interpret martian spectral data collected in-situ. The focus was on finding spectral features that can be detected by the cameras on Mars and are diagnostic of specific minerals. The samples are a collection of (1) Fe/Mg-phyllosilicates from submarine hydrothermal sites and (2) of rocks from acid alteration environments containing goethite, hematite, jarosite and Fe-bearing chlorite as these minerals are detectable in the extended visible range. Among all the samples, interstratified glauconite-nontronite has the most unique spectral features and should be easily detectable with the rover cameras. The spectral features of talc from Fe-bearing interstratified specimens are described. These data are especially relevant as glauconite and talc have been proposed to be fairly abundant on Mars and their detections are suggested from remote-sensing near-IR data. Several indices are proposed to assess Fe content on the investigated samples as well as mineral concentration of goethite and hematite. Among these indices, the normalized spectral slope in the range 420–600 nm increases with total Fe content for all samples, whether phyllosilicates, oxides or sulphates (R2 = 0.7–0.8). For pure phyllosilicates, the slope from 600 to 1010 nm decreases with increasing octahedral Fe (R2 = 0.75). An index for goethite produced excellent results assessing goethite concentration (R2 = 0.84). Of all cameras, Mast Camera reproduces the spectra with lowest fidelity and generates the poorest correlations between indices and tested variables. The other three cameras perform similarly. [Display omitted] • Lab spectra of Earth analogues shown with the resolution of martian rover cameras. • Spectral fidelity of Fe-clays and Fe oxides is: IMP, PanCam, MastCam-Z > MastCam. • Interstratified glauconite-nontronite easily recognizable on Mars by rover cameras. • Spectral features of Fe-rich talc and interstratified talc layers are shown. • Spectral indexes correlate well with Fe content and goethite content in samples. [ABSTRACT FROM AUTHOR]

Abstract: Aluminous clay deposits on Mars are recognized from remotely sensed infrared spectral features similar to those of montmorillonite, beidellite, and/or kaolinite. The nature of aluminous clay deposits on Mars is of interest because they likely indicate a different formation mechanism than that of Fe–Mg clays, which are widespread on Mars and likely alteration products of the Fe–Mg-rich basaltic crust. The near-infrared reflectance spectra of aluminous martian clay deposits frequently display characteristics typical of both montmorillonite and kaolinite. The question arises whether such mixed character is due to the existence of end-member phases or to kaolinite–smectite mixed-layer (K–S). The issue is relevant because K–S implies the existence of a smectite precursor that alters into kaolinite, and thus constrains the timing and intensity of the alteration processes that generates it. A mixture of kaolinite and smectite end-members may indicate locally heterogeneous alteration processes, or alternatively, could result from the physical mixing of altered materials of different provenance. A group of natural K–S samples and synthetic kaolinite/smectite mixtures of known proportion, all of which had been thoroughly characterized in previous work using several analytical techniques, were investigated here using near-infrared (NIR) spectroscopy. The NIR spectral features correlate well with their kaolinite–smectite relative proportions. The shape of spectral features attributed to Al–OH in K–S is subtly different from those in physical mixtures of kaolinite and smectite. Based on qualitative comparison, some regions on Mars appear to have spectral signatures similar to K–S. We also applied a quantitative technique using the second derivative of spectra. In this technique, plots of the height of the features at (λ=) 2.21μm (band present in kaolinite and montmorillonite) and 2.17μm (kaolinite only) were able to discriminate between K–S and kaolinite–smectite physical mixtures, as they generated correlations with different slopes. The method of discrimination was applied to Mars spectra, which resulted in reasonable evidence for the existence of K–S in Nili Fossae and Mawrth Vallis, and mixtures of end-members in Mawrth Vallis and Leighton Crater. This is one of the first times that evidence for mixed-layer clay minerals, and particularly K–S, on Mars has been gathered. The ability to detect mixed-layer clays is an important step forward for further development of our understanding of the processes that generated clay on Mars. [Copyright &y& Elsevier]

Abstract: Amino acid–smectite interaction may have catalyzed prebiotic reactions essential for the emergence of life. Lysine solutions (0.05 M) were reacted with Na-smectite in adsorption–desorption experiments. The lysine–smectite complexes were heated at 80 °C for 10 days to investigate (1) possible slow processes taking place at surface temperature that would be accelerated at higher temperature and (2) processes taking place in hydrothermal systems. Three sets of experiments were performed: thermal treatment in closed tubes and water added regularly; thermal treatment in closed tubes without adding water; and thermal treatment in open tubes and no added water. After lysine desorption (displacement with 0.1 M CaCl2), the solutions were investigated using circular dichroism (CD) and the smectite samples using FTIR and CHN elemental analysis. CD spectra were dependent on the solution pH, which was controlled by lysine protonation state. The lysine protonation state was altered by the adsorption–desorption process, with a higher Lys+/Lys± ratio after desorption. The CD and CHN analyses show that the thermal treatment in a moist state causes stronger smectite–lysine binding. FTIR data suggest that the stronger binding is caused by more or stronger H bonds between –NH+ 3 lysine groups and smectite basal O atoms. [Copyright &y& Elsevier]

The detection of organic molecules associated with life on Mars is one of the main goals of future life-searching missions such as the ESA-Roscosmos ExoMars and NASA 2020 mission. In this work we studied the preservation of 25 amino acids that were spiked onto the Mars-relevant minerals augite, enstatite, goethite, gypsum, hematite, jarosite, labradorite, montmorillonite, nontronite, olivine and saponite, and on basaltic lava under simulated Mars conditions. Simulations were performed using the Open University Mars Chamber, which mimicked the main aspects of the martian environment, such as temperature, UV radiation and atmospheric pressure. Quantification and enantiomeric separation of the amino acids were performed using gas-chromatography-mass spectrometry (GC–MS). Results show that no amino acids could be detected on the mineral samples spiked with 1 µM amino acid solution (0.1 µmol of amino acid per gram of mineral) subjected to simulation, possibly due to complete degradation of the amino acids and/or low extractability of the amino acids from the minerals. For higher amino acid concentrations, nontronite had the highest preservation rate in the experiments in which 50 µM spiking solution was used (5 µmol/g), while jarosite and gypsum had a higher preservation rate in the experiments in which 25 and 10 µM spiking solutions were used (2.5 and 1 µmol/g), respectively. Overall, the 3 smectite minerals (montmorillonite, saponite, nontronite) and the two sulfates (gypsum, jarosite) preserved the highest amino acid proportions. Our data suggest that clay minerals preserve amino acids due to their high surface areas and small pore sizes, whereas sulfates protect amino acids likely due to their opacity to UV radiation or by partial dissolution and crystallization and trapping of the amino acids. Minerals containing ferrous iron (such as augite, enstatite and basaltic lava) preserved the lowest amount of amino acids, which is explained by iron (II) catalyzed reactions with reactive oxygen species generated under Mars-like conditions. Olivine (forsterite) preserved more amino acids than the other non-clay silicates due to low or absent ferrous iron. Our results show that D- and L-amino acids are degraded at equal rates, and that there is a certain correlation between preservation/degradation of amino acids and their molecular structure: alkyl substitution in the α-carbon seem to contribute towards amino acid stability under UV radiation. These results contribute towards a better selection of sampling sites for the search of biomarkers on future life detection missions on the surface of Mars. [ABSTRACT FROM AUTHOR]