Janice L. Bishop

Mineralogic and compositional properties of Martian soil and dust: Results from Mars Pathfinder

Mars Pathfinder obtained multispectral, elemental, magnetic, and physical measurements of soil and dust at the Sagan Memorial Station during the course of its 83 sol mission. We describe initial results from these measurements, concentrating on multispectral and elemental data, and use these data, along with previous Viking, SNC meteorite, and telescopic results, to help constrain the origin and evolution of Martian soil and dust. We find that soils and dust can be divided into at least eight distinct spectral units, based on parameterization of Imager for Mars Pathfinder (IMP) 400 to 1000 nm multispectral images. The most distinctive spectral parameters for soils and dust are the reflectivity in the red, the red/blue reflectivity ratio, the near-IR spectral slope, and the strength of the 800 to 1000 nm absorption feature. Most of the Pathfinder spectra are consistent with the presence of poorly crystalline or nanophase ferric oxide(s), sometimes mixed with small but varying degrees of well-crystalline ferric and ferrous phases. Darker soil units appear to be coarser-grained, compacted, and/or mixed with a larger amount of dark ferrous materials relative to bright soils. Nanophase goethite, akaganeite, schwertmannite, and maghemite are leading candidates for the origin of the absorption centered near 900 nm in IMP spectra. The ferrous component in the soil cannot be well-constrained based on IMP data. Alpha proton X-ray spectrometer (APXS) measurements of six soil units show little variability within the landing site and show remarkable overall similarity to the average Viking-derived soil elemental composition. Differences exist between Viking and Pathfinder soils, however, including significantly higher S and Cl abundances and lower Si abundances in Viking soils and the lack of a correlation between Ti and Fe in Pathfinder soils. No significant linear correlations were observed between IMP spectral properties and APXS elemental chemistry. Attempts at constraining the mineralogy of soils and dust using normative calculations involving mixtures of smectites and silicate and oxide minerals did not yield physically acceptable solutions. We attempted to use the Pathfinder results to constrain a number of putative soil and dust formation scenarios, including palagonitization and acid-fog weathering. While the Pathfinder soils cannot be chemically linked to the Pathfinder rocks by palagonitization, this study and McSween et al. [1999] suggest that palagonitic alteration of a Martian basaltic rock, plus mixture with a minor component of locally derived andesitic rock fragments, could be consistent with the observed soil APXS and IMP properties.

Roter Kamm impact crater, Namibia: Geochemistry of basement rocks and breccias

Abstract The Roter Kamm crater in the southern Namib Desert has previously been identified as an impact structure on the basis of crater morphology and the presence of impact melt breccias which contain shock metamorphosed quartz and lithic clasts. To better define the variety of target rocks and breccias, we studied the petrography and chemical composition of a new suite of twenty-eight basement and breccia samples from the Roter Kamm crater. Based on chemical data for target lithologies and breccias we suggest that the crater was formed in a two-layer target region: an upper layer of Gariep metasediments (schist, marble, ± quartzite and sandstone) overlying the crystalline basement of the Namaqualand Metamorphic Complex. The basement was also heavily intruded by coarse-grained quartz veins and quartz- and quartz-feldspar pegmatites. The clast population in the melt breccias indicates that impact-induced melting involved mainly metasedimentary target rocks, with rarely detected contributions from pegmatite and granite/granodiorite. Three varieties of melt breccias can be defined: (1) “schistose,” (2) quartzitic melt breccias, (3) “true” impact melt breccias. These melt breccia types are chemically heterogeneous, and even the impact melt breccias may have been produced in situ and not from a coherent melt body. The shapes of the schistose melt breccias, previously thought to be ejected impact breccias, are most likely caused by erosion, and these breccias are now interpreted to be locally derived. The crater basement as exposed at the rim was structurally severely affected and, at least locally, considerable thermal energy was generated during formation of large volumes of cataclastic, mylonitic, and pseudotachylitic breccias. Analyses of mylonite and pseudotachylites from the crater rim, as well as their respective host rocks, show that these breccias were mainly formed from local material. Analyses of pseudotachylite-like breccias indicate that these possible friction melts are generated by preferential melting of hydrous ferromagnesian minerals and feldspar, similar to their tectonically produced counterparts. Although no significant fluid effects resulting from formation of mylonites or pseudotachylites are indicated, several breccias (compared to their host rocks) do show evidence of severe chemical alteration (chloritisation and sericitisation). The presence of large vesicles filled with hydrothermal mineral assemblages in some schistose breccias and other petrographic and chemical data support the hypothesis of an impact-induced hydrothermal event in the crater area.

Reflectance and Mossbauer spectroscopy of ferrihydrite-montmorillonite assemblages as Mars soil analog materials.

Spectroscopic analyses show that Fe(3+)-doped smectites prepared in the laboratory exhibit important similarities to the soils on Mars. Ferrihydrite has been identified as the interlayer ferric component in Fe(3+)-doped smectites by a low quadrupole splitting and magnetic field strength of approximately 48 tesla in Mossbauer spectra measured at 4.2 K, as well as a crystal field transition at 0.92 micrometer. Ferrihydrite in these smectites explains features in the visible-near infrared region that resemble the energies and band strengths of features in reflectance spectra observed for several bright regions on Mars. Clay silicates have met resistance in the past as Mars soil analogs because terrestrial clay silicates exhibit prominent hydrous spectral features at 1.4, 1.9, and 2.2 micrometers; and these are observed weakly, if at all, in reflectance spectra of Mars. However, several mechanisms can weaken or compress these features, including desiccation under low-humidity conditions. The hydration properties of the interlayer cations also effect band strengths, such that a ferrihydrite-bearing smectite in the Martian environment would exhibit a 1.9 micrometers H2O absorption that is even weaker than the 2.2 micrometers structural OH absorption. Mixing experiments demonstrate that infrared spectral features of clays can be significantly suppressed and that the reflectance can be significantly darkened by mixing with only a few percent of a strongly absorbing opaque material. Therefore, the absolute reflectance of a soil on Mars may be disproportionately sensitive to a minor component. For this reason, the shape and position of spectral features and the chemical composition of potential analogs are of utmost importance in assessing the composition of the soil on Mars. Given the remarkable similarity between visible-infrared reflectance spectra of soils in bright regions on Mars and Fe(3+)-doped montmorillonites, coupled with recent observations of smectites in SNC meteorites and a weak 2.2 micrometers absorption in some Mars soils, ferrihydrite-bearing smectites warrant serious consideration as a Mars soil analog.