The processes that formed hydrated minerals on Mars remain unconstrained. A suite of minerals including all mineralogical classes known on Mars (clays, sulfates and oxides) has been identified in Noctis Labyrinthus. The particular mineralogical association and proximity to settings of volcanic activity suggests coeval formation in a unique local hydrothermal environment.
Two troughs in Noctis Labyrinthus display a diversity of mineral assemblages rarely seen spatially collocated on Mars. Minerals identified from Mars Reconnaissance Orbiter data within the troughs include polyhydrated and monohydrated sulfates, an Al clay (e. g., kaolinite or beidellite), Fe/Mg smectites, hydrated silica and/or opal, and a leached clay or jarosite mixture with a doublet absorption between 2.2 and 2.3 mu m. Units both pre-date and post-date smaller pits and depressions within the larger troughs, indicating that deposition was coeval with continued extension, collapse, and erosion in the Late Hesperian to Early Amazonian (2-3 Ga). The strata within each trough display a mineralogic diversity consistent with active aqueous processes and/or changing chemical conditions over time, perhaps due to hydrothermal alteration of volcanic ash, influxes of groundwater from nearby Tharsis volcanism, fumarole activity, and melting snow and/or ice. The superposition of younger Fe/Mg smectites over sulfates, Al clays, and hydrated silica and/or opal in both troughs indicates that this region is unique relative to most other locations on Mars, where the opposite progression is observed and the Fe/Mg smectites are Noachian (older than 3.6 Ga) in age. Consequently, these troughs may have been habitable regions on Mars at a time when drier conditions dominated the surface.
Sedimentary deposits within the 280 km wide crater containing Aram Chaos (∼3°N, 339°E) have been differentially eroded by wind to expose a stratigraphic column 900–1000 m thick that unconformably overlies the chaos bedrock. A detailed stratigraphic and mineralogical description of the deposits is presented based on data from the Mars Reconnaissance Orbiter Compact Reconnaissance Imaging Spectrometer for Mars, Context Imager, and High Resolution Imaging Science Experiment. Two sedimentary units overlie the basement chaos material representing the original plains fill in Aram Crater: the first and oldest is composed of (1) a 50–75 m thick dark‐toned basal unit containing ferric hydroxysulfate intercalated with monohydrated‐sulfate‐bearing materials, (2) a 75–100 m thick light‐toned unit with monohydrated sulfates, and (3) a 175–350 m thick light‐toned resistant capping unit with nanophase ferric oxides and monohydrated sulfates. After a period of wind erosion, these deposits were partially and unconformably covered by the second sedimentary unit, a 75–100 m thick, discontinuous dark‐toned unit containing crystalline hematite and polyhydrated sulfate material. These sedimentary deposits were formed by evaporite deposition during at least two distinct rising groundwater episodes fed by regional‐scale recharge. Later groundwater event(s) formed the polyhydrated materials, indicating that environmental conditions changed to a higher water‐to‐rock ratio. Wind has continued to shape the landscape after the last wetting event to produce the features and exposures observed.
Previous orbital mapping of crystalline gray haematite, ferric oxides, and sulfates has shown an association of this mineralogy with light-toned, layered deposits on the floor of Valles Marineris, in chaos terrains in the canyon's outflow channels, and in Meridiani Planum. The exact nature of the relationship between ferric oxides and sulfates within Valles Marineris is uncertain. The Observatoire pour la Mineralogie, l'Eau, les Glaces et l'Activite (OMEGA) spectrometer initially identified sulfate and ferric oxides in the layered deposits of Valles Marineris. The Thermal Emission Spectrometer (TES) has also mapped coarse (gray) haematite in or at the base of these deposits. We use Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) spectra and Context Camera (CTX) and High Resolution Imaging Science Experiment (HiRISE) imagery from the Mars Reconnaissance Orbiter (MRO) to explore the mineralogy and morphology of the large layered deposit in central Capri Chasma, part of the Valles Marineris canyon system that has large, clear exposures of sulfate and haematite. We find kieserite (MgSO4·H2O) and ferric oxide (often crystalline red haematite) in the lower bedrock exposures and a polyhydrated sulfate without ferric oxides in the upper bedrock. This stratigraphy is duplicated in many other basinal chasmata, suggesting a common genesis. We propose the haematite and monohydrated sulfate formed by diagenetic alteration of a sulfate-rich sedimentary deposit, where the upper polyhydrated sulfate-rich, haematite-poor layers either were not buried sufficiently to convert to a monohydrated sulfate or were part of a later depositional phase. Based on the similarities between the Valles Marineris assemblages and the sulfate and haematite-rich deposits of Meridiani Planum, we hypothesize a common evaporite and diagenetic formation process for the Meridiani Planum sediments and the sulfate-bearing basinal Interior Layered Deposits.
The region surrounding the Mawrth Vallis outflow channel on Mars hosts thick layered deposits containing diverse phyllosilicate minerals. Here we report detection of the Ca-sulfate bassanite on the outflow channel floor, requiring a more complex aqueous chemistry than previously inferred for this region. The sulfate-bearing materials underlie phyllosilicate-bearing strata, and provide an opportunity for testing proposed models of martian geochemical evolution with a future landed mission.
New high-resolution spectral and morphologic imaging of deposits on walls and floor of Ius Chasma extend previous geomorphic mapping, and permit a new interpretation of aqueous processes that occurred during the development of Valles Marineris. We identify hydrated mineralogy based on visible-near infrared (VNIR) absorptions. We map the extents of these units with CRISM spectral data as well as morphologies in CTX and HiRISE imagery. Three cross-sections across Ius Chasma illustrate the interpreted mineral stratigraphy. Multiple episodes formed and transported hydrated minerals within Ius Chasma. Polyhydrated sulfate and kieserite are found within a closed basin at the lowest elevations in the chasma. They may have been precipitates in a closed basin or diagenetically altered after deposition. Fluvial or aeolian processes then deposited layered Fe/Mg smectite and hydrated silicate on the chasma floor, postdating the sulfates. The smectite apparently was weathered out of Noachian-age wallrock and transported to the depositional sites. The overlying hydrated silicate is interpreted to be an acid-leached phyllosilicate transformed from the underlying smectite unit, or a smectite/jarosite mixture. The finely layered smectite and massive hydrated silicate units have an erosional unconformity between them, that marks a change in surface water chemistry. Landslides transported large blocks of wallrock, some altered to contain Fe/Mg smectite, to the chasma floor. After the last episode of normal faulting and subsequent landslides, opal was transported short distances into the chasma from a few m-thick light-toned layer near the top of the wallrock, by sapping channels in Louros Valles. Alternatively, the material was transported into the chasma and then altered to opal. The superposition of different types of hydrated minerals and the different fluvial morphologies of the units containing them indicate sequential, distinct aqueous environments, characterized by alkaline, then circum-neutral, and finally very acidic surface or groundwater chemistry.
MAJOR GEOLOGICAL DISCONTINUITIES IN THE WALLS OF VALLES MARINERIS, MARS. J. Flahaut1, J. F. Mustard2, C. Quantin1, H. Clenet1, P. Allemand1, P. Thomas1, G. Dromart1 and L. H. Roach2. 1Laboratoire de Science de la Terre, UMR CNRS 5570, Université Claude Bernard/Ecole Normale Supérieure de Lyon, 2 rue Raphaël Dubois, 696222 Villeurbanne Cedex, France (jessica.flahaut@ens-lyon.fr). 2Department of Geological Sciences, Brown University, Providence, RI 02912.
Juventae Chasma contains four light‐toned sulfate‐bearing mounds (denoted here as A–D from west to east) inside the trough, mafic outcrops at the base of the mounds and in the wall rock, and light‐toned layered deposits of opal and ferric sulfates on the plateau. Hyperspectral visible/near‐infrared Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) spectra were used to identify monohydrated and polyhydrated sulfate (PHS) outcrops of layered material on the bright mounds. Most of the monohydrated sulfate signatures closely resemble those of szomolnokite (FeSO 4 ·H 2 O), characterized by a water band near 2.08 μ m, while some areas exhibit spectral features more similar to those of kieserite (MgSO 4 ·H 2 O), with a band centered closer to 2.13 μ m. The largest PHS outcrops occur on the top of mound B, and their spectral features are most consistent with ferricopiapite, melanterite, and starkeyite, but a specific mineral cannot be uniquely identified at this time. Coordinated analyses of CRISM maps, Mars Orbiter Laser Altimeter elevations, and High Resolution Imaging Science Experiment images suggest that mounds A and B may have formed together and then eroded into separate mounds, while mounds C and D likely formed separately. Mafic minerals (low‐Ca pyroxene, high‐Ca pyroxene, and olivine) are observed in large ∼2–10 km wide outcrops in the wall rock and in smaller outcrops ∼50–500 m across at the floor of the canyon. Most of the wall rock is covered by at least a thin layer of dust and does not exhibit strong features characteristic of these minerals. The plateau region northwest of Juventae Chasma is characterized by an abundance of light‐toned layered deposits. One region contains two spectrally unique phases exhibiting a highly stratified, terraced pattern. CRISM spectra of one unit eroded into swirling patterns with arc‐like ridges exhibit a narrow 2.23‐ μ m band assigned to hydroxylated ferric sulfate. A thin layer of a fractured material bearing an opaline silica phase is observed at the contact between the older plateau unit and the younger hydroxylated ferric sulfate‐bearing light‐toned layered deposits. Hydrothermal processes may have produced an acidic environment that fostered formation of the hydrated silica and hydroxylated ferric sulfate units.
This paper brings together initial results obtained of the high northern latitudes in Mars years 28 and 29, between October 2006 and October 2008. These measurements confirm many previous models and shed new light on the nature of polar surface materials, particularly in intermediate‐albedo units of the polar layered deposits, many of which are found to be ice‐rich. We identify hydrated non ice materials present in many low‐albedo troughs, as well as in the circumpolar erg that was previously associated with gypsum. We identify icy outlier deposits that may be related to subsurface thermophysical properties and permafrost. New observations of the gypsum‐rich dune material constrain models for its formation and distribution. Intrinsic properties of ice content and grain size are found to be independent of the albedo of fine layered units and may provide a novel method for stratigraphic identification and correlation.
The Noachian terrain west of the Isidis basin hosts a diverse collection of alteration minerals in rocks comprising varied geomorphic units within a 100,000 km 2 region in and near the Nili Fossae. Prior investigations in this region by the Observatoire pour l'Minéralogie, l'Eau, les Glaces, et l'Activité (OMEGA) instrument on Mars Express revealed large exposures of both mafic minerals and iron magnesium phyllosilicates in stratigraphic context. Expanding on the discoveries of OMEGA, the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) aboard the Mars Reconnaissance Orbiter (MRO) has found more spatially widespread and mineralogically diverse alteration minerals than previously realized, which represent multiple aqueous environments. Using CRISM near‐infrared spectral data, we detail the basis for identification of iron and magnesium smectites (including both nontronite and more Mg‐rich varieties), chlorite, prehnite, serpentine, kaolinite, potassium mica (illite or muscovite), hydrated (opaline) silica, the sodium zeolite analcime, and magnesium carbonate. The detection of serpentine and analcime on Mars is reported here for the first time. We detail the geomorphic context of these minerals using data from high‐resolution imagers onboard MRO in conjunction with CRISM. We find that the distribution of alteration minerals is not homogeneous; rather, they occur in provinces with distinctive assemblages of alteration minerals. Key findings are (1) a distinctive stratigraphy, in and around the Nili Fossae, of kaolinite and magnesium carbonate in bedrock units always overlying Fe/Mg smectites and (2) evidence for mineral phases and assemblages indicative of low‐grade metamorphic or hydrothermal aqueous alteration in cratered terrains. The alteration minerals around the Nili Fossae are more typical of those resulting from neutral to alkaline conditions rather than acidic conditions, which appear to have dominated much of Mars. Moreover, the mineralogic diversity and geologic context of alteration minerals found in the region around the Nili Fossae indicates several episodes of aqueous activity in multiple distinct environments.