JpGU-AGU Joint Meeting 2017

Presentation information

[JJ] Oral

M (Multidisciplinary and Interdisciplinary) » M-IS Intersection

[M-IS26] [JJ] Aqua planetology

Sat. May 20, 2017 9:00 AM - 10:30 AM 103 (International Conference Hall 1F)

convener:Yasuhito Sekine(Department of Earth and Planetary Science, University of Tokyo), Takazo Shibuya(Japan Agency for Marine-Earth Science and Technology), Hidenori Genda(Earth-Life Sicence Institute, Tokyo Institute of Technology), Keisuke Fukushi(Institute of Nature & Environmental Technology, Kanazawa University), Chairperson:Yasuhito Sekine(Department of Earth and Planetary Science, University of Tokyo), Chairperson:Takazo Shibuya(JAMSTEC)

10:00 AM - 10:15 AM

[MIS26-05] EXPERIMENTAL STUDY ON MANGANESE OXIDE FORMATION: INTERPRETAION OF MANGANESE OXIDE ON GALE CRATER AND OXIDIZING ENVIRONMENT ON EARLY MARS.

*Natsumi Noda1, Shoko Imamura1, Yasuhito Sekine1, Soichiro Uesugi1, Minako Kurisu1, Chihiro Miyamoto1, Haruhisa Tabata1, Yoshio Takahashi1, Takashi Murakami1 (1. Department of Earth and Planetary Science, The University of Tokyo)

Keywords:Early Mars, Planetary environment, Atmospheric evolution

The Curiosity rover has found Mn enrichments within sandstones in the Kimberley region of the Gale crater on Mars [1]. These enrichments were detected within fracture-filling materials, i.e., veins, crosscutting the surrounding sandstones, implying that Mn was once concentrated in subsurface fluids and then precipitated within ancient aquifers [1]. The chemical composition analysis for the Mn-rich materials also show that the abundance of Mn is coupled with those of transition trace metals, particularly Ni and Zn; meanwhile, Si, Ca, Cl and/or S are inversely correlated or not correlated with Mn [1]. This indicates that Mn exists as oxides in the fracture-filling materials, rather than silicate, carbonate, or chloride [1]. Since oxidation of Mn requires high levels of redox potential [2], the findings of Mn oxides indicate a possible coexistence of a highly oxidizing atmosphere and wet conditions on early Mars [1]. However, the pO2 level at the time of deposition of Mn oxides remains poorly constrained.
In the present study, we conducted laboratory experiments in order to constrain the pO2 level at the time of deposition of the Mn oxides based on the elemental pattern of coprecipitation of Mn oxides. In the experiments, we synthesized MnO2, Mn3O4, and Mn(OH)2 from solutions of dissolved Mn, Ni, Zn, and Cr using different oxidants, such as KMnO4 [8] or H2O2 [9]. After the reactions, filtered solutions and solid precipitates were collected. The recovered solid precipitates were analyzed with X-ray absorption fine structure (XAFS) and X-ray diffraction (XRD). In addition, concentrations of dissolved Mn, Cr, Ni, and Zn in the remnant solution samples were measured using inductively coupled plasma atomic emission spectroscopy (ICP-AES). We found that only formation of MnO2 can explain the enrichments of Mn together with Ni and Zn, which is consistent with the pattern of trace metal enrichments of the Mn oxides in the Gale crater. On the other hand, formations of Mn3O4 or Mn(OH)2 cannot account for the observations. Given that precipitation of MnO2 requires a high level of O2 (>0.01 bar), our results strongly suggest the presence of an O2-rich atmosphere on early Mars at the time when groundwater was active within the Gale crater. These results, in turn, imply effective formation of O2 via H2O photolysis and/or ineffective loss of O2 due to limited amounts of reductants on early Mars.

References: [1] Lanza, N.L. et al. (2016). Geophys. Res. Lett., 43, 7398-7407. [2] Usui, A. et al. (2015). Geoscience of Marine Manganese Deposits, 1st ed., University of Tokyo Press. [3] Holland, H.D. (1984). Princeton Univ. Press, Princeton, NJ. 582 pp. [4] Forget, F. & Pierrehumbert, R.T. (1997). Science 278:1273-76 [5] Wordsworth, R.D. (2016). Annu. Rev. Earth Planet. Sci. 44, 381-408 [6] Noda, N.et al. (2017). LPSC abstract, 48th, 1786 [7] Imamura, S. et al. (2017). JpGU, this meeting [8] Uesugi, S. (2017) master’s thesis [9] Mu, J. et al. (2006). Journal of Dispersion Sci. and Tech. 27:1223-1225