Modified clay minerals on Mars: Sedimentary rocks exposed in Gale crater on Mars contain extensive clay minerals. Bristow et al. analyzed drill samples collected by the Curiosity rover as it climbed up sedimentary layers in the crater. They found evidence of past reactions with liquid water and sulfate brines, which could have percolated through the clay from an overlying sulfate deposit. Similar sulfate deposits are widespread across the planet and represent some of the last sedimentary rocks to form before the planet lost its surface liquid water, so the results inform our understanding of the geologic processes that occurred as Mars dried out. Science, abg5449, this issue p. 198

The Glen Torridon (GT) region in Gale crater, Mars is a region with strong clay mineral signatures inferred from orbital spectroscopy. The CheMin X‐ray diffraction (XRD) instrument onboard the Mars Science Laboratory rover, Curiosity, measured some of the highest clay mineral abundances to date within GT, complementing the orbital detections. GT may also be unique because in the XRD patterns of some samples, CheMin identified new phases, including: (a) Fe‐carbonates, and (b) a phase with a novel peak at 9.2 Å. Fe‐carbonates have been previously suggested from other instruments onboard, but this is the first definitive reporting by CheMin of Fe‐carbonate. This new phase with a 9.2 Å reflection has never been observed in Gale crater and may be a new mineral for Mars, but discrete identification still remains enigmatic because no single phase on Earth is able to account for all of the GT mineralogical, geochemical, and sedimentological constraints. Here, we modeled XRD profiles and propose an interstratified clay mineral, specifically greenalite‐minnesotaite, as a reasonable candidate. The coexistence of Fe‐carbonate and Fe‐rich clay minerals in the GT samples supports a conceptual model of a lacustrine groundwater mixing environment. Groundwater interaction with percolating lake waters in the sediments is common in terrestrial lacustrine settings, and the diffusion of two distinct water bodies within the subsurface can create a geochemical gradient and unique mineral front in the sediments. Ultimately, the proximity to this mixing zone may have controlled the secondary minerals preserved in sedimentary rocks exposed in GT.

The Curiosity rover's exploration of rocks and soils in Gale crater has provided diverse geochemical and mineralogical data sets, underscoring the complex geological history of the region. We report the crystalline, clay mineral, and amorphous phase distributions of four Gale crater rocks from an 80‐m stratigraphic interval. The mineralogy of the four samples is strongly influenced by aqueous alteration processes, including variations in water chemistries, redox, pH, and temperature. Localized hydrothermal events are evidenced by gray hematite and maturation of amorphous SiO₂ to opal‐CT. Low‐temperature diagenetic events are associated with fluctuating lake levels, evaporative events, and groundwater infiltration. Among all mudstones analyzed in Gale crater, the diversity in diagenetic processes is primarily captured by the mineralogy and X‐ray amorphous chemistry of the drilled rocks. Variations indicate a transition from magnetite to hematite and an increase in matrix‐associated sulfates suggesting intensifying influence from oxic, diagenetic fluids upsection. Furthermore, diagenetic fluid pathways are shown to be strongly affected by unconformities and sedimentary transitions, as evidenced by the intensity of alteration inferred from the mineralogy of sediments sampled adjacent to stratigraphic contacts.

For the first time on Mars, the crystalline magnesium‐sulfate mineral starkeyite (MgSO ₄ ‧4H ₂ O) was definitively identified using the CheMin X‐ray diffraction instrument at Gale crater. At the Canaima drill site, starkeyite along with amorphous MgSO ₄ ‧ n H ₂ O are among the “polyhydrated Mg‐sulfates” interpreted in orbital reflectance spectra. Mg‐sulfates are good climate indicators as they are very responsive to changes in temperature and relative humidity. We hypothesize that, through evaporation, Mg‐sulfates formed at the end of brine evolution when ion concentrations became saturated and precipitated on the surface or near sub‐surface as either epsomite or meridianiite. These minerals were subsequently dehydrated later to starkeyite and amorphous MgSO ₄ ‧ n H ₂ O in response to a drier Mars. At Canaima, starkeyite is stable and would form during the warmer Mars summers. Due to very slow kinetics at the low Mars winter temperatures, starkeyite and amorphous MgSO ₄ ‧ n H ₂ O would be resistant to recrystallize to more hydrous forms and thus likely persist year‐round. During the course of analyses, starkeyite transforms into amorphous MgSO ₄ ‧ n H ₂ O inside the rover body due to the elevated temperature and greatly reduced relative humidity compared to the martian surface at the Canaima drill site. It is possible that crystalline sulfate minerals existed in earlier samples measured by CheMin but altered inside the rover before they could be analyzed. Starkeyite is most likely prevalent in the subsurface, whereas both starkeyite and amorphous MgSO ₄ ‧ n H ₂ O are likely present on the surface as starkeyite could partially transform into amorphous MgSO ₄ ‧ n H ₂ O due to direct solar heating.