Statistical analysis of APXS-derived chemistry of the clay-bearing Glen Torridon region and Mount Sharp group, Gale crater, Mars

1C. D. O’Connell-Cooper,1L. M. Thompson,1J. G. Spray,2J. A. Berger,3R. Gellert,3M. McCraig,4S. J. VanBommel,5A. Yen
Journal of Geophysical Research (Planets) (in Press) Link to Article [https://doi.org/10.1029/2021JE007177]
1Planetary and Space Science Centre, University of New Brunswick, Fredericton, Canada
2NASA Johnson Space Center, Houston, TX, USA
3University of Guelph, Ontario, Canada
4Washington University, St Louis, MO, USA
5Jet Propulsion Laboratory, California Institute of Technology, Pasadena, CA, USA
Published by arrangement with John Wiley & Sons

The Glen Torridon stratigraphic sequence marks the transition from the low energy lacustrine-dominated Murray formation (Mf) (Jura member: Jm) to the more diverse Carolyn Shoemaker formation (CSf) (Knockfarril Hill member: Knockfarril Hill; Glasgow member: Glasgow). This transition defines a change in depositional setting. Alpha Particle X-ray Spectrometer (APXS) results and statistical analysis reveal that the bulk primary geochemistry of Mf targets are broadly in family with CSf targets, but with subtle compositional and diagenetic trends with increasing elevation. APXS results reveal significant compositional differences between Jura_GT and the stratigraphically equivalent Jura on Vera Rubin ridge (Jura_VRR). The data define two geochemical facies (high-K or high-Mg), with a strong bimodal grain distribution in Jura_GT and Knockfarril Hill. The contact between Knockfarril Hill and Glasgow is marked by abrupt sedimentological changes but a similar composition for both. Away from the contact, the Knockfarril Hill and Glasgow plot discretely, suggesting a zone of common alteration at the transition and/or a gradual transition in provenance with increasing elevation in the Glasgow member. APXS results point to a complex history of diagenesis within Glen Torridon, with increasing diagenesis close to the Basal Siccar Point unconformity on the Greenheugh pediment, and with proximity to the beginning of the clay sulfate transition. Elemental mobility is evident in localized enrichments or depletions in Ca, S, Mn, P, Zn, Ni. The highly altered Hutton interval, in contact with the unconformity on Tower butte, is also identified on Western Butte, indicating that the “interval” was once laterally extensive.

Global Hydrogen Abundances on the Lunar Surface

1David J. Lawrence,1Patrick N. Peplowski,1Jack T. Wilson,2Richard C. Elphic
Journal of Geophysical research (Planets) (in Press) Open Access Link to Article [https://doi.org/10.1029/2022JE007197]
1Johns Hopkins University Applied Physics Laboratory, Laurel, Maryland, United States
2NASA Ames Spaceflight Center, Moffett Field, California, United States
Published by arrangement with John Wiley & Sons

A global map of bulk hydrogen abundances on the Moon is presented. This map was generated using data from the Lunar Prospector Neutron Spectrometer. This map required corrections for variations due to rare-earth elements, and was calibrated to Apollo sample hydrogen abundances. Since neutron-derived measurements sample hydrogen content to a depth of tens of cm, these results provide complementary insights to those provided by studies using spectral reflectance data, which sample depths of order μm. Comparison of these abundances to Apollo sample values suggest that the samples reflect actual hydrogen content on the lunar surface, not dominantly from non-lunar contamination. The average lunar hydrogen abundance is 47 ppm with a systematic uncertainty of ∼10 ppm. This is consistent with bulk hydrogen from solar wind emplacement. A bulk hydrogen enhancement (50–68 ppm) has been identified at the Moon’s largest pyroclastic deposit (Aristarchus Plateau), which corroborates prior observations that hydrogen and/or water plays a role in lunar magmatic events. Global data show a correlation between hydrogen and evolved materials rich in incompatible trace elements (i.e., KREEP type rocks), with a hydrogen excess of 14–36 ppm in these materials. Based on this hydrogen enhancement, we estimate a lower-limit water abundance within urKREEP materials (i.e., the final ∼2% of the lunar magma ocean) of 320–820 ppm H2O. This observation implies that water played a role in the original magma-ocean formation and solidification with a lower-limit water content in the original lunar magma ocean of 7–16 ppm or higher.