Mineralogical Investigation of Mg‐Sulfate at the Canaima Drill Site, Gale Crater, Mars
- Creators
- Chipera, S. J.
- Vaniman, D. T.
- Rampe, E. B.
- Bristow, T. F.
- Martínez, G.
- Tu, V. M.
- Peretyazhko, T. S.
- Yen, A. S.
- Gellert, R.
- Berger, J. A.
- Rapin, W.
- Morris, R. V.
- Ming, D. W.
- Thompson, L. M.
- Simpson, S.
- Achilles, C. N.
- Tutolo, B.
- Downs, R. T.
- Fraeman, A. A.
- Fischer, E.
- Blake, D. F.
- Treiman, A. H.
- Morrison, S. M.
- Thorpe, M. T.
- Gupta, S.
- Dietrich, W. E.
- Downs, G.
- Castle, N.
- Craig, P. I.
- Des Marais, D. J.
- Hazen, R. M.
- Vasavada, A. R.
- Hausrath, E.
- Sarrazin, P.
- Grotzinger, J. P.1
Abstract
For the first time on Mars, the crystalline magnesium-sulfate mineral starkeyite (MgSO4‧4H2O) was definitively identified using the CheMin X-ray diffraction instrument at Gale crater. At the Canaima drill site, starkeyite along with amorphous MgSO4‧nH2O 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 MgSO4‧nH2O 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 MgSO4‧nH2O would be resistant to recrystallize to more hydrous forms and thus likely persist year-round. During the course of analyses, starkeyite transforms into amorphous MgSO4‧nH2O 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 MgSO4‧nH2O are likely present on the surface as starkeyite could partially transform into amorphous MgSO4‧nH2O due to direct solar heating.
Copyright and License
© 2023. The Authors. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Acknowledgement
We thank M. Velbel, R. Peterson, and 2 anonymous reviewers for helping improve the manuscript. We acknowledge the support of the Jet Propulsion Lab engineering and management teams and MSL science team members who participated in tactical and strategic operations, without whom the data presented here could not have been collected. Some of this research was carried out at the Jet Propulsion Laboratory, California Institute of Technology, under a contract with the National Aeronautics and Space Administration (NASA). Some co-authors acknowledged funding from the MSL Participating Scientist Program. The MSL APXS instrument and operations were supported by the Canadian Space Agency contract 9F52-19-0632. E.F work was carried out under a contract with the National Aeronautics and Space Administration (NASA) contract 1449038.
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Additional details
- ISSN
- 2169-9100
- National Aeronautics and Space Administration
- 1449038
- Canadian Space Agency
- 9F52‐19‐0632
- Caltech groups
- Division of Geological and Planetary Sciences