Constraints on the crystal-chemistry of Fe/Mg-rich smectitic clays on Mars and links to global alteration trends

Near-infrared remote sensing data of Mars have revealed thousands of ancient deposits of Fe/Mg-rich smectitic clay minerals within the crust with relevance to past habitability. Diagnostic metal-OH infrared spectroscopic absorptions used to interpret the mineralogy of these phyllosilicates occur at wavelengths of 2.27-2.32 mu m, indicating variable Fe/Mg ratios in the clay structures. The objective of this work is to use these near infrared absorptions to constrain the mineralogy of smectites on Mars. Using Fe/Mg-rich seafloor clay minerals as mineralogical and spectroscopic analogs for Martian clay minerals, we show how crystal-chemical substitution and mixed layering affect the position of the diagnostic metal-OH spectral feature in smectitic clay minerals. Crystal-chemistry of smectites detected on Mars were quantitatively constrained with infrared data and categorized into four mineralogical groups. Possible alteration processes are constrained by comparisons of clay chemistry detected by remote sensing techniques to the chemistry of candidate protoliths. Of the four groups identified, three of them indicate significant segregation of Fe from Mg, suggestive of alteration under water-rich and/or oxidizing conditions on Mars. The fourth group (with low Fe/Mg ratios) may result from alteration in reducing or water-limited conditions, potentially in subsurface environments. Some samples are interstratified di-trioctahedral clay minerals that have characteristics of dioctahedral clay minerals but clear chemical evidence for trioctahedral sheets. Approximately 70% of smectite deposits previously detected on Mars are classified as Fe-rich (FeO/MgO > 10). Only 22% of detections are trioctahedral and relatively Mg-rich. An additional similar to 8% are difficult to characterize, but might be very Fe-rich. The segregation of Fe from Mg in Martian clay minerals suggests that Mg should be enriched in other contemporaneous deposits such as chlorides and carbonates. (C) 2015 The Authors. Published by Elsevier B.V.