X-ray amorphous material that is variably Mg/Fe/Si-rich and Al-poor and that likely contains secondary alteration products is prevalent in Gale crater sediments and rocks (15-73 wt.%). However, the structure and origin of these materials and their implications for past environmental conditions remain unknown. In this study, we use transmission electron microscopy and synchrotron microprobe analyses to examine Mg/Fe/Si-rich and Al-poor ultramafic soils from the warm Mediterranean climate Klamath Mountains of California and cold subarctic climate Tablelands of Newfoundland, Canada to help interpret environmental conditions during the formation of chemically similar X-ray amorphous material in Gale crater, Mars. Primary glass is absent from the Klamath Mountains and Tablelands materials; secondary X-ray amorphous material includes globular amorphous silica and chemically heterogeneous nanospherical amorphous material and nanocrystalline phases. Globular amorphous silica is only present in soils that undergo extensive periods of cyclic freezing. Fe-containing X-ray amorphous material from the subarctic Tablelands is significantly richer in Mg and Si than X-ray amorphous material from the warmer Klamath Mountains. Fe-rich nanocrystallites contain more Mg and Si in the subarctic Tablelands but are more highly Fe-enriched in the warmer Klamath Mountains. Potential secondary nanocrystalline phyllosilicates are only observed in the warmest examined soil in the Klamath Mountains. These characteristics – the presence or absence of amorphous silica, the chemical composition of X-ray amorphous material, the abundance and composition of Fe-rich nanocrystallites, and the presence or absence of secondary phyllosilicates - provide helpful identifiers to interpret past environmental conditions during the formation of X-ray amorphous material on Mars.

During the first 2934 sols of the Curiosity rover’s mission 33,468 passive visible/near-infrared reflectance spectra were taken of the surface by the mast-mounted ChemCam instrument on a range of target types. ChemCam spectra of bedrock targets from the Murray and Carolyn Shoemaker formations on Mt. Sharp were investigated using principal component analysis (PCA) and various spectral parameters including the band depth at 535 nm and the slope between 840 nm and 750 nm. Four endmember spectra were identified. Passive spectra were compared to Laser Induced Breakdown Spectroscopy (LIBS) data to search for correlations between spectral properties and elemental abundances. The correlation coefficient between FeOT reported by LIBS and BD535 from passive spectra was used to search for regions where iron may have been added to the bedrock through oxidation of ferrous-bearing fluids, but no correlations were found. Rocks in the Blunts Point-Sutton Island transition that have unique spectral properties compared to surrounding rocks, that is flat near-infrared (NIR) slopes and weak 535 nm absorptions, are associated with higher Mn and Mg in the LIBS spectra of bedrock. Additionally, calcium-sulfate cements, previously identified by Ca and S enrichments in the LIBS spectra of bedrock, were also shown to be associated with spectral trends seen in Blunts Point. A shift towards steeper near-infrared slope is seen in the Hutton interval, indicative of changing depositional conditions or increased diagenesis.

Images from the Mars Science Laboratory (MSL) mission of lacustrine sedimentary rocks of Vera Rubin ridge on “Mt. Sharp” in Gale crater, Mars, have shown stark color variations from red to purple to gray. These color differences cross-cut stratigraphy and are likely due to diagenetic alteration of the sediments after deposition. However, the chemistry and timing of these fluid interactions is unclear. Determining how diagenetic processes may have modified chemical and mineralogical signatures of ancient martian environments is critical for understanding the past habitability of Mars and achieving the goals of the MSL mission. Here we use visible/near-infrared spectra from Mastcam and ChemCam to determine the mineralogical origins of color variations in the ridge. Color variations are consistent with changes in spectral properties related to the crystallinity, grain size, and texture of hematite. Coarse-grained gray hematite spectrally dominates in the gray patches and is present in the purple areas, while nanophase and fine-grained red crystalline hematite are present and spectrally dominate in the red and purple areas. We hypothesize that these differences were caused by grain size coarsening of hematite by diagenetic fluids, as observed in terrestrial analogs. In this model, early primary reddening by oxidizing fluids near the surface was followed during or after burial by bleaching to form the gray patches, possibly with limited secondary reddening after exhumation. Diagenetic alteration may have diminished the preservation of biosignatures and changed the composition of the sediments, making it more difficult to interpret how conditions evolved in the paleolake over time.