Spectral reflectance properties of minerals exposed to simulated Mars surface conditions

A number of mineral species were exposed to martian surface conditions of atmospheric pressure and composition, temperature, and UV light regime, and their evolution was monitored using reflectance spectroscopy. The stabilities for different groups varied widely. Phyllosilicate spectra all showed measurable losses of interlayer H₂O, with some structural groups showing more rapid H₂O loss than others. Loss of OH from the phyllosilicates is not always accompanied by a change in metal-OH overtone absorption bands. OH-bearing sulfates, such as jarosite and alunite, show no measurable change in spectral properties, suggesting that they should be spectrally detectable on Mars on the basis of diagnostic absorption bands in the 0.4-2.5 μm region. Fe³⁺- and H₂O-bearing sulfates all showed changes in the appearance and/or reduction in depths of hydroxo-bridged Fe³⁺ absorption bands, particularly at 0.43 μm. The spectral changes were often accompanied by visible color changes, suggesting that subsurface sulfates exposed to the martian surface environment may undergo measurable changes in reflectance spectra and color over short periods of time (days to weeks). Organic-bearing geological materials showed no measurable change in CH related absorption bands, while carbonates and hydroxides also showed no systematic changes in spectral properties. The addition of ultraviolet irradiation did not seem to affect mineral stability or rate of spectral change, with one exception (hexahydrite). In some cases, spectral changes could be related to the formation of specific new phases. The data also suggest that hydrated minerals detected on Mars to date retain their diagnostic spectral properties that allow their unique identification.     

Spectral evidence for zeolite in the dust on Mars

Spectral features observed in Mars Global Surveyor Thermal Emission Spectrometer data (∼1670-220 cm⁻¹) of martian surface dust provide clues to its mineralogy. An emissivity peak at ∼1630 cm⁻¹ is consistent with the presence of an H₂O-bearing mineral. This spectral feature can be mapped globally and shows a distribution related to the classical bright regions on Mars that are known to be dust covered. An important spectral feature at ∼830 cm⁻¹ present in a newly derived average spectrum of surface dust likely is a transparency feature arising from the fine particulate nature of the dust. Its shape and location are consistent with plagioclase feldspars and also zeolites, which essentially are the hydrous form of feldspar. The generally favored visible/near-infrared spectral analog for martian dust, JSC Mars-1 altered tephra, does not display the ∼830 cm⁻¹ feature. Zeolites commonly form from the interaction of low temperature aqueous fluids and volcanic glass in a variety of geologic settings. The combination of spectral features that are consistent with zeolites and the likelihood that Mars has (or had) geologic conditions necessary to produce them makes a strong case for recognizing zeolite minerals as likely components of the martian regolith.     

Mineralogy of Terra Meridiani and western Arabia Terra from OMEGA/MEx and implications for their formation

Analyses of Mars Express OMEGA hyperspectral data (0.4-2.7 μm) for Terra Meridiani and western Arabia Terra show that the northern mantled cratered terrains are covered by dust that is spectrally dominated by nanophase ferric oxides. Dark aeolian dunes inside craters and dark streaks extending from the dunes into the intercrater areas in mantled cratered terrains in western Arabia Terra have similar pyroxene-rich signatures demonstrating that the dunes supply dark basaltic material to create dark streaks. The dissected cratered terrains to the south of the mantled terrains are dominated spectrally by both low-calcium and high-calcium pyroxenes with abundances of 20-30% each retrieved from nonlinear radiative transfer modeling. Spectra over the hematite-bearing plains in Meridiani Planum are characterized by very weak but unique spectral features attributed to a mixture of a dark and featureless component (possibly gray hematite) and minor olivine in some locations. Hydrated minerals (likely hydrous ferric sulfates and/or hydrous hydroxides) associated with poorly ferric crystalline phases are found in the etched terrains to the north and east of the hematite-bearing plains where erosion has exposed ∼1 km of section of layered outcrops with high thermal inertias. These materials are also found in numerous craters in the northern Terra Meridiani and may represent outliers of the etched terrain materials. A few localized spots within the etched terrain also exhibit the spectral signature of Fe-rich phyllosilicates. The ensemble of observations show that the evidence for aqueous processes detected by the Opportunity Rover in Meridiani Planum is widespread and confirms the extended presence of surface or near-surface water over this large region of Mars. The scenarios of formation of Terra Meridiani (“dirty” acidic evaporite, impact surge or weathering of volcanic ash) cannot satisfactorily explain the mineralogy derived from the OMEGA observations. The formation of the etched terrains is consistent with leaching of iron sulfides and formation of sulfates and hydrated iron oxides, either in-place or via transport and evaporation of aqueous fluids and under aqueous conditions less acidic than inferred from rocks examined by Opportunity.     

Properties of the hermean regolith: iii. disk-resolved vis-NIR reflectance spectra and implications for the abundance of iron

Disk-resolved reflectance spectra of the surface of Mercury (longitudes 240-300°), obtained in the visual (vis) and near-infrared (NIR) spectral region, are presented and analyzed. The observations were made at the 2.6-m Nordic Optical Telescope with the ALFOSC low-resolution spectrograph on 20 and 22 June 1999 in the wavelength range 520-970 nm with a footprint size of 700 km on the mid-disk of Mercury. A method which enables more accurate correction for telluric line absorptions and atmospheric extinction than that applied on previously published vis-NIR spectra of Mercury is introduced. The resulting reflectance spectra are remarkably linear, lack significant absorption features, and have optical slopes comparable to remotely sensed lunar pure anorthosites. The relation between spectral slope and photometric geometry found by Warell (2002, Icarus 156, 313-317) is confirmed and is explained as caused by strongly backscattering particles with embedded submicroscopic metallic iron in a mature regolith. With the theoretical maturation model of Hapke (2001, J. Geophys. Res. 106 (E5), 10039-10073) an abundance of 0.05-0.3 wt% submicroscopic metallic iron in the regolith for silicate grain sizes in the range 10-80 μm is determined, implying a ferrous iron content in mafic minerals intrinsically lower than that of the lunar highlands. A binary crustal composition model with anorthite linearly mixed with pyroxene provides better spectral fits than a pure anorthitic composition. Comparison with mature lunar pure anorthosite spectra yields a confident upper limit to the FeO content of 3 wt% under the assumption that the surfaces are similarly matured, but this figure probably represents a considerable overestimate. The average mercurian regolith does not seem to be substantially more weathered than the most mature lunar highland soils in terms of abundance of submicroscopic metallic iron, indicating that a steady-state maturation level has been reached. However, the strong relation between optical spectral slope and photometric geometry may imply that the majority of regolith particles are more fine-grained than their lunar counterparts and that the regolith is admixed with complex agglutinate weathering products which are more abundant and more transparent than those of the lunar highlands. This is consistent with more energetic impacts and a higher rate of impact melt production in an iron-poor regolith. An observed relation between the spectral slope and latitude provides evidence that the Ostwald ripening process may be operating at equatorial latitudes on Mercury.     

Mercury's albedo from Mariner 10: Implications for the presence of ferrous iron

Mariner 10 clear filter (490 nm) images of Mercury were recalibrated and photometrically normalized to produce a mosaic of nearly an entire hemisphere of the planet. Albedo contrasts are slightly larger than seen in the lunar highlands (excluding maria). Variegations indicative of compositional differences include diffuse low albedo units often overlain by smooth plains, the high albedo smooth plains of Borealis Planitia, and high-albedo enigmatic crater floor deposits. A higher level of contrast between immature crater ejecta and average mature material on Mercury compared to the Moon is consistent with a more intense space weathering environment on Mercury that results in a more mature regolith. Immature lunar highlands materials are ∼1.5 times higher in reflectance than analogous immature mercurian materials. Immature materials of the same composition would have the same reflectance on both bodies, thus this observation requires that Mercury's crust contains a significant darkening agent, either opaque minerals or ferrous iron bearing silicates, in abundances significantly higher than those of the lunar highlands. If the darkening agent is opaque minerals (e.g. ilmenite or ulvospinel) Mercury's crust may contain significant ferrous iron and yet not exhibit a 1-μm absorption band.     

Flood-formed dunes in Athabasca Valles, Mars: morphology, modeling, and implications

Estimates of discharge for martian outflow channels have spanned orders of magnitude due in part to uncertainties in floodwater height. A methodology of estimating discharge based on bedforms would reduce some of this uncertainty. Such a methodology based on the morphology and granulometry of flood-formed (‘diluvial’) dunes has been developed by Carling (1996b, in: Branson, J., Brown, A.G., Gregory, K.J. (Eds.), Global Continental Changes: The Context of Palaeohydrology. Geological Society Special Publication No. 115, London, UK, 165-179) and applied to Pleistocene flood-formed dunes in Siberia. Transverse periodic dune-like bedforms in Athabasca Valles, Mars, have previously been classified both as flood-formed dunes and as antidunes. Either interpretation is important, as they both imply substantial quantities of water, but each has different hydraulic implications. We undertook photoclinometric measurements of these forms, and compared them with data from flood-formed dunes in Siberia. Our analysis of those data shows their morphology to be more consistent with dunes than antidunes, thus providing the first documentation of flood-formed dunes on Mars. Other reasoning based on context and likely hydraulics also supports the bedforms' classification as dunes. Evidence does not support the dunes being aeolian, although a conclusive determination cannot be made with present data. Given the preponderance of evidence that the features are flood-formed instead of aeolian, we applied Carling's (1996b, in: Branson, J., Brown, A.G., Gregory, K.J. (Eds.), Global Continental Changes: The Context of Palaeohydrology. Geological Society Special Publication No. 115, London, UK, 165-179) dune-flow model to derive the peak discharge of the flood flow that formed them. The resultant estimate is approximately 2×10⁶ m³/s, similar to previous estimates. The size of the Athabascan dunes' in comparison with that of terrestrial dunes suggests that these martian dunes took at least 1-2 days to grow. Their flattened morphology implies that they were formed at high subcritical flow and that the flood flow that formed them receded very quickly.     

Thermal alteration of nontronite and montmorillonite: Implications for the martian surface

To test the effects of meteorite impacts on martian phyllosilicate deposits, we heated two smectites (nontronite and montmorillonite) to temperatures ranging from 350 °C to 1150 °C for durations of 4-24 h in two different atmospheres, under air and a steady flow of CO₂. Samples were analyzed using X-ray diffraction (XRD) and near-infrared (NIR) and mid-infrared (MIR) reflectance spectroscopy. Interlayer water was lost after heating to temperatures of ∼400 °C. Between 400 °C and 700 °C, nontronite converted to an intermediary phase which conserved the XRD pattern of untreated nontronite with the exception of the 0 0 1 peak. Nanocrystalline high-temperature phases formed for both smectites at temperatures between 700 °C and 1000 °C. Finally, after being heated to temperatures above ∼1100 °C, the samples melted and recrystallized into secondary phases. Secondary high-temperature phases included sillimanite and cristobalite for both smectites plus hematite for nontronite. NIR and MIR reflectance spectra significantly evolved with increasing temperature. NIR spectra of smectites showed that 1.4 and 1.9 μm bands decrease in intensity and disappear above 700 °C. Similarly, the 2.2-2.3 μm metal-OH band showed a decrease in intensity as well as an overall shift towards lower wavelengths (for nontronite) due to the thermal resistance of the Al-OH bond compared to the Fe-OH bond. NIR spectra of montmorillonite showed a gradual increase in band depth up to temperatures between 500 °C and 600 °C, then decreased with increasing temperature. In the MIR spectra of samples heated to temperatures above ∼1100 °C, newly formed bands confirmed the secondary phases identified by XRD. Similarities between the NIR spectra of our heated samples and the phyllosilicates in some martian craters imply that these phyllosilicates were altered by the impact-generated heat and thus were not formed post-impact. In addition, NIR reflectance spectra provide a proxy for shock temperatures of smectites up to 700 °C while MIR is optimum for identification of high-temperature phases of smectites above 700 °C.     

The 0.7-5.3 μm IR spectra of Mercury and the Moon: Evidence for high-Ca clinopyroxene on Mercury

We present infrared spectra of Mercury and the Moon in the wavelength range 0.7-5.3 μm obtained with the SpeX spectrograph at the NASA Infrared Telescope Facility. The spectra were acquired from pole and terminator locations of Mercury's surface and of Mersenius C and the Copernicus central peak on the Moon. Spectra of both bodies were measured in close temporal succession and were reduced in the same manner with identical calibration stars to minimize differences in the reduction process. The Copernicus spectra display the expected absorption features due to mafic minerals in the near infrared and show spectral features in the SiO combination/overtone vibrational band region above 4 μm. The spectra of Mercury from longitude 170° and north and south mid-latitudes display a 1-μm absorption band indicative of high-Ca clinopyroxene, while a spectrum from longitude 260° and northern mid-latitudes does not. The Mercury spectra show a broad feature of low emittance over the full 3-5 μm thermal infrared region, but no narrow features in this spectral range. The longitude 260° spectrum shows excess thermal emission around 5 μm attributable to the existence of a thermal gradient in the insolated dayside regolith. The thermal-IR spectra suggest a significant difference in the compositional and/or structural properties of Mercury and the Moon that may be due to grain size, absorption coefficient, or the magnitude of near-surface thermal gradients. The results indicate that the composition of Mercury's surface is heterogeneous on regional scales, and that the near infrared wavelength range provides more discriminative information on the surface composition than the 2-4 μm region, where the solar reflected and thermally emitted radiation contribute approximately equally to the observed flux of these bodies.     

Interpretation of Mars southern highlands high amplitude magnetic field with total gradient and fractal source modeling: New insights into the magnetic mystery of Mars

Using model studies, the total gradient (TG) of the Z-component magnetic field is shown to be a useful quantity for delineating sources of satellite-altitude magnetic anomalies; this field is used to constrain the location and lateral boundaries of sources of high amplitude magnetic anomalies of southern highlands of Mars. The TG field suggests two parallel linear and oppositely magnetized sources of 1000 and 1800 km length separated by 1000 km of region of intervening non-parallel sources. The simplest interpretation of the long, linear features is that they are zones of multitudinous crustal scale dikes formed in separate episodes of rifting, and not features associated with the mechanism of seafloor spreading. Forward modeling with uniformly magnetized sources suggests that magnetizations of the order of 10-50 A/m (40 km thickness) over ∼100 km width in the case of the southern source and of 12.5-27.5 A/m (40 km thickness) and ∼200 km width for the northern source are necessary to explain the Z-component amplitudes and features of the TG field. If the crustal magnetization on Mars were to be distributed fractally as on Earth, magnetizations matching the largest amplitude features on Mars may be spatially correlated from a 50-100 km distance range (β ∼ 3) to approaching nearly uniform magnetization (β ∼ 5) values. To keep magnetization intensity as small as possible, the higher end of β values are preferred, whereas, small amplitude anomaly features could be generated from sources with β ∼ 3. Many of the Mars anomaly features could be coalescence effects similar to the coalescence of anomaly features observed on http://icarus.cornell.edu/information/keywords.html.Earth.     

Correlations between hematite and sulfates in the chaotic terrain east of Valles Marineris

We have identified the presence of polyhydrated sulfates in association with crystalline gray hematite in outcrop units of the chaotic terrain east of Valles Marineris. The hematite is found in abundances of up to ∼18%, and is usually associated with thin (∼10's of meters) cliff-forming layers of intermediate-toned outcrops (albedo ∼0.15-0.20) as well as mantling deposits adjacent to the outcrops. The polyhydrated sulfates are usually restricted to the bedrock unit, and are not found in the adjacent mantling units. In analogy to the observations performed at the Opportunity landing site, we hypothesize that erosion of the sulfate/hematite-bearing outcrops leaves the hematite behind as a lag and breaks the sulfates down to wind-transportable sizes. We also find that the layered outcrops present, for the most part, embayment or on-lap relationships with respect to the hummocks that constitute the chaotic terrain, suggesting that these units were emplaced via subaqueous or aeolian deposition and/or flow after the event that formed the associated chaos. These morphological observations, in conjunction with the correlation between hematite and polyhydrated sulfates also suggest an aqueous genesis for the crystalline gray hematite in these chaotic units, and presents evidence for the action of aqueous processes after the formation of at least some of the chaotic units on Mars.     

Properties of the Hermean regolith: V. New optical reflectance spectra, comparison with lunar anorthosites, and mineralogical modelling

We present new optical (0.4-0.65 μm) spectra of Mercury and lunar pure anorthosite locations, obtained quasi-simultaneously with the Nordic Optical Telescope (NOT) in 2002. A comparative study is performed with the model of Lucey et al. (2000, J. Geophys. Res. 105, 20297-20305, and references therein) between iron-poor, mature, pure anorthosite (>90% plagioclase feldspar) Clementine spectra from the lunar farside and a combined 0.4-1.0 μm mercurian spectrum, obtained with the NOT, calculated for standard photometric geometry. Mercury is located at more extreme locations in the Lucey ratio-reflectance diagrams than any known lunar soil, specifically with respect to the extremely iron-poor mature anorthosites. Though quantitative prediction of FeO and TiO₂ abundances cannot be made without a more generally applicable model, we find qualitatively that the abundances of both these oxides must be near zero for Mercury. We utilize the theory of Hapke (2002, Icarus 157, 523-534, and references therein), with realistic photometric parameters, to model laboratory spectra of matured mineral powders and lunar soils, and remotely sensed spectra of lunar anorthosites and Mercury. An important difference between fabricated and natural powders is the high value for the internal scattering parameter necessary to interpret the spectra for the former, and the requirement of rough and non-isotropically scattering surfaces in the modelling of the latter. The mature lunar anorthosite spectra were well modelled with binary mixtures of calcic feldspars and olivines, grain sizes of 25-30 μm and a concentration of submicroscopic metallic iron (SMFe) of 0.12-0.15% in grain coatings. The mercurian spectrum is not possible to interpret from terrestrial mineral powder spectra without introducing an average particle scattering function for the bulk soil that increases in backscattering efficiency with wavelength. The observed spectrum is somewhat better predicted with binary mixture models of feldspars and pyroxenes, than with single-component regoliths consisting of either albite or diopside. Correct spectral reflectance values were predicted with a concentration of 0.1 wt% SMFe in coatings of 15-30 μm sized grains. Since reasonable cosmogonical formation scenarios for Mercury, or meteoritic infall, predict iron concentrations at least this high, we draw the conclusion that the average grain size of Mercury is about a factor of two smaller than for average returned lunar soil samples. The 0.6-2.5 μm spectrum of McCord and Clark (1979, J. Geophys. Res. 178, 745-747) is used to further limit the possible range of mineralogical composition of Mercury. It is found that an intimately mixed and matured 3:1 labradorite-to-enstatite regolith composition best matches both the optical and near-infrared spectra, yielding an abundance of ∼1.2 wt% FeO and ∼0 wt% TiO₂.     

Mineralogical constraints on the high-silica martian surface component observed by TES

The Thermal Emission Spectrometer (TES) has observed a high-silica material in the dark regions of Mars that is spectrally similar to obsidian glass and may have a volcanic origin. An alternate interpretation is that the spectrally amorphous material consists of clay minerals or some other secondary material, formed by chemical alteration of surface rocks. The regions where this material is observed (e.g., Acidalia Planitia) have relatively high spectral contrast, suggesting that the high-silica material exists as coarse particulates, indurated soils or cements, within rocks, or as indurated coatings on rock surfaces. The geologic interpretation of this spectral result has major implications for understanding magmatic evolution and weathering processes on Mars. One of the complications in interpreting spectral observations of glasses and clay minerals is that both are structurally and compositionally complex. In this study, we perform a detailed spectroscopic analysis of indurated smectite clay minerals and relate their thermal emission spectral features to structural and crystal chemical properties. We examine the spectral similarities and differences between smectite clay minerals and obsidian glass from a structural-chemical perspective, and make further mineralogical interpretations from previous TES results. The results suggest that neither smectite clays nor any clay mineral with similar structural and chemical properties can adequately explain TES observations of high-silica materials in some martian dark regions. If the spectrally amorphous materials observed by TES do represent an alteration product, then these materials are likely to be poorly crystalline aluminosilicates. While all clay minerals have Si/O ratios ?0.4, the position of the emissivity minimum at Mars suggests a Si/O ratio of 0.4-0.5. The spectral observation could be explained by the existence of a silica-rich alteration product, such as Al- or Fe-bearing opal, an intimate physical mixture of relatively pure silica and other aluminosilicates (such as clay minerals or clay precursors), or certain zeolites. The chemical alteration of basaltic rocks on Mars to phyllosilicate-poor, silica-rich alteration products provides a geologically reasonable and consistent explanation for the global TES surface mineralogical results.     

Preferential low-pH dissolution of pyroxene in plagioclase-pyroxene mixtures: Implications for martian surface materials

Acid weathering of plagioclase-pyroxene mixtures has been investigated with an open system kinetic dissolution model. The modeling reveals that elevated plagioclase/pyroxene ratios observed in some low-albedo martian regions and atmospheric dust could be partially caused by preferential dissolution of pyroxenes at pHs below ∼3-4. Surface materials with smaller grain sizes, affected by lower pH fluids, and/or exposed to longer durations of acid weathering would be enriched in plagioclase. If preferential dissolution is responsible for the observed mineral ratios, the dissolution process likely occurred on a large scale, such as weathering by acid atmospheric precipitates. If dissolution was continuous, modeled timeframes required to produce a high plagioclase/pyroxene ratio are short on geologic timescales; however, it is likely that acid weathering on Mars was episodic, possibly occurring over a longer period of time.     

A study of the properties of a local dust storm with Mars Express OMEGA and PFS data

We present observations of a local dust storm performed by the OMEGA and PFS instruments aboard Mars Express. OMEGA observations are used to retrieve the dust single-scattering albedo in the spectral range 0.4-4.0 μm. The single-scattering albedo shows fairly constant values between 0.6 and 2.6 μm, and a sharp decrease at wavelengths shorter than 0.6 μm, in agreement with previous studies. It presents a small absorption feature due to ferric oxide at 0.9 μm, and a strong absorption feature due to hydrated minerals between 2.7 and 3.6 μm. We use a statistical method, the Independent Component Analysis, to determine that the dust spectral signature is decoupled from the surface albedo, proving that the retrieval of the single-scattering albedo is reliable, and we map the dust optical thickness with a conventional radiative transfer model. The effect of the dust storm on the atmospheric thermal structure is measured using PFS observations. We also simulate the thermal impact of the dust storm using a one-dimensional atmospheric model. A comparison of the retrieved and modeled temperature structures suggests that the dust in the storm should be confined to the 1-2 lowest scale heights of the atmosphere. However, the observed OMEGA reflectance in the CO₂ absorption bands does not support this suggestion.     

Discovery of jarosite within the Mawrth Vallis region of Mars: Implications for the geologic history of the region

Analysis of visible to near infrared reflectance data from the MRO CRISM hyperspectral imager has revealed the presence of an ovoid-shaped landform, approximately 3 by 5 km in size, within the layered terrains surrounding the Mawrth Vallis outflow channel. This feature has spectral absorption features consistent with the presence of the ferric sulfate mineral jarosite, specifically a K-bearing jarosite (KFe₃(SO₄)₂(OH)₆). Terrestrial jarosite is formed through the oxidation of iron sulfides in acidic environments or from basaltic precursor minerals with the addition of sulfur. Previously identified phyllosilicates in the Mawrth Vallis layered terrains include a basal sequence of layers containing Fe-Mg smectites and an upper set of layers of hydrated silica and aluminous phyllosilicates. In terms of its fine scale morphology revealed by MRO HiRISE imagery, the jarosite-bearing unit has fracture patterns very similar to that observed in Fe-Mg smectite-bearing layers, but unlike that observed in the Al-bearing phyllosilicate unit. The ovoid-shaped landform is situated in an east-west bowl-shaped depression superposed on a north sloping surface. Spectra of the ovoid-shaped jarosite-bearing landform also display an anomalously high 600 nm shoulder, which may be consistent with the presence of goethite and a 1.92 μm absorption which could indicate the presence of ferrihydrite. Goethite, jarosite, and ferrihydrite can be co-precipitated and/or form through transformation of schwertmannite, both processes generally occurring under low pH conditions (pH 2-4). To date, this location appears to be unique in the Mawrth Vallis region and could represent precipitation of jarosite in acidic, sulfur-rich ponded water during the waning stages of drying.     

Generation and performance of automated jarosite mineral detectors for visible/near-infrared spectrometers at Mars

We have developed two automated detectors that can recognize the sulfate mineral jarosite in unknown visible to near-infrared spectra (350-2500 nm). The two detectors are optimized for use within the terrestrial and martian atmospheres. The detectors are built from Support Vector Machines trained using a generative model to create linear mixtures of library mineral spectra. Both detectors performed with an average ∼90% accuracy on laboratory spectra of single minerals and the laboratory and field spectra of rocks collected in a hydrothermal environment. This type of algorithm will contribute to the efficiency of onboard data analysis of landed and orbital visible/near-infrared spectrometers at Mars.     

Constraints on Mercury’s surface composition from MESSENGER and ground-based spectroscopy

The composition and chemistry of Mercury’s regolith has been calculated from MESSENGER MASCS 0.3-1.3 μm spectra from the first flyby, using an implementation of Hapke’s radiative transfer-based photometric model for light scattering in semi-transparent porous media, and a linear spectral mixing algorithm. We combine this investigation with linear spectral fitting results from mid-infrared spectra and compare derived oxide abundances with mercurian formation models and lunar samples. Hapke modeling results indicate a regolith that is optically dominated by finely comminuted particles with average area weighted grain size near 20 μm. Mercury shows lunar-style space weathering, with maturation-produced microphase iron present at ∼0.065 wt.% abundance, with only small variations between mature and immature sites, the amount of which is unable to explain Mercury’s low brightness relative to the Moon. The average modal mineralogies for the flyby 1 spectra derived from Hapke modeling are 35-70% Na-rich plagioclase or orthoclase, up to 30% Mg-rich clinopyroxene, <5% Mg-rich orthopyroxene, minute olivine, ∼20-45% low-Fe, low-Ti agglutinitic glass, and <10% of one or more lunar-like opaque minerals. Mercurian average oxide abundances derived from Hapke models and mid-infrared linear fitting include 40-50 wt.% SiO₂, 10-35 wt.% Al₂O₃, 1-8 wt.% FeO, and <25 wt.% TiO₂; the inferred rock type is basalt. Lunar-like opaques or glasses with high Fe and/or Ti abundances cannot on their own, or in combination, explain Mercury’s low brightness. The linear mixing results indicate the presence of clinopyroxenes that contain up to 21 wt.% MnO and the presence of a Mn-rich hedenbergite. Mn in M1 crystalline lattice sites of hedenbergite suppresses the strong 1 and 2 μm crystal field absorption bands and may thus act as a strong darkening agent on Mercury. Also, one or more of thermally darkened silicates, Fe-poor opaques and matured glasses, or Mercury-unique Ostwald-ripened microphase iron nickel may lower the albedo. A major part of the total microphase iron present in Mercury’s regolith is likely derived from FeO that is not intrinsic to the crust but has been subsequently delivered by exogenic sources.     

Assessing the limits of the Modified Gaussian Model for remote spectroscopic studies of pyroxenes on Mars

We investigate the ability to refine pyroxene composition and modal abundance from laboratory and remotely acquired spectra. Laboratory data including the martian meteorites, Shergotty, Zagami, MIL03346, and ALH84001 as well as additional pyroxene-rich spectra obtained from the OMEGA (Observatoire pour la Minéralogie, l'Eau, les Glaces, et l'Activité) spectrometer for Mars are characterized using the Modified Gaussian Model (MGM), a spectral deconvolution method developed by Sunshine et al. [Sunshine, J.M., Pieters, C.M., Pratt, S., 1990. J. Geophys. Res. 95, 6955-6966]. We develop two sensitivity tests to assess the extent to which the MGM can consistently predict (1) pyroxene composition and (2) modal abundance for a compositionally diverse suite of pyroxene spectra. Results of the sensitivity tests indicate that the MGM can be appropriately applied to remote spectroscopic measurements of extraterrestrial surfaces and can estimate pyroxene composition and relative abundance within a derived uncertainty. Deconvolved band positions for laboratory spectra of the meteorites Shergotty and Zagami are determined within ±17 nm while remotely acquired OMEGA spectra are defined within ±50 nm. These results suggest that absolute compositions can be uniquely derived from laboratory pyroxene-rich spectra and non-uniquely derived from the remote measurements of OMEGA at this time. While relative pyroxene chemistries are not assessed from OMEGA measurements at this time, relative pyroxene abundances are estimated using a normalized band strength ratio between the low-calcium (LCP) and high-calcium (HCP) endmember components and are constrained to ±10%. The fraction of LCP in a two-pyroxene mixture is the derived value from the normalized band strength ratio, LCP/(LCP + HCP). This calculation for relative abundance is robust in the presence of up to 10-15% olivine. Deconvolution results from the OMEGA spectra indicate that the ancient terrain in the Syrtis Major region is uniquely enriched in LCP (59±10% LCP) relative to HCP while the volcanics of Syrtis Major are uniquely enriched in HCP (39±10% LCP).     

Geomorphic knobs of Candor Chasma, Mars: New Mars Reconnaissance Orbiter data and comparisons to terrestrial analogs

High Resolution Imaging Science Experiment (HiRISE) imagery and digital elevation models of the Candor Chasma region of Valles Marineris, Mars, reveal prominent and distinctive positive-relief knobs amidst light-toned layers. Three classifications of knobs, Types 1, 2, and 3, are distinguished from a combination of HiRISE and Thermal Emission Imaging System (THEMIS) images based on physical expressions (geometries, spatial relationships), and spectral data from Compact Reconnaissance Imaging Spectrometer for Mars (CRISM). Type 1 knobs are abundant, concentrated, topographically resistant features with their highest frequency in West Candor, which have consistent stratigraphic correlations of the peak altitude (height). These Type 1 knobs could be erosional remnants of a simple dissected terrain, possibly derived from a more continuous, resistant, capping layer of pre-existing material diagenetically altered through recrystallization or cementation. Types 2 and 3 knobs are not linked to a single stratigraphic layer and are generally solitary to isolated, with variable heights. Type 3 are the largest knobs at nearly an order of magnitude larger than Type 1 knobs. The variable sizes and occasional pits on the tops of Type 2 and 3 knobs suggest a different origin, possibly related to more developed erosion, preferential cementation, or textural differences from sediment/water injection or intrusion, or from a buried impact crater. Enhanced color HiRISE images show a brown coloration of the knob peak crests that is attributable to processing and photometric effects; CRISM data do not show any detectable spectral differences between the knobs and the host rock layers, other than albedo. These intriguing knobs hold important clues to deducing relative rock properties, timing of events, and weathering conditions of Mars history.     

A search for basaltic-to-intermediate glasses on Mars: Assessing martian crustal mineralogy

Multiple datasets have demonstrated that the crust of Mars is fundamentally basaltic. However, spectral libraries used to interrogate thermal infrared spectra of Martian dark regions through spectral deconvolution have heretofore lacked mafic glasses despite the importance of amorphous phases (or phases with amorphous-like spectral signatures) in Martian mineralogy. To establish the presence and importance of basaltic-to-intermediate glasses in Martian lithologies, we created five such glasses, obtained their thermal infrared spectra and included the spectra in a library used to deconvolve nine regional Thermal Emission Spectrometer spectra from Mars. We employed the nonnegative least squares (NNLS) deconvolution method, which yields deconvolved phase abundances and the uncertainties associated with those abundances. The basaltic-to-intermediate glasses do not appear in the deconvolution solutions, indicating they are not globally or regionally important phases. Because Martian igneous or impact processes are capable of basaltic-to-intermediate glass formation, the lack of such glasses in the deconvolved mineralogies suggests either the glasses did not form in detectable quantities or they (or their signatures) have been removed. The masking or replacement of basaltic-to-intermediate glasses through alteration is supported by the appearance in the deconvolution solutions of amorphous phases (e.g., silica-rich glasses, opal) or phases with amorphous-like spectral signatures (e.g., clays, zeolites) that commonly form through aqueous alteration of mafic glasses. The glasses may still be important to local-scale thermal infrared studies given the basaltic nature of Mars and the variety of local-scale lithologies detected by various missions. The regional mineralogies derived from the NNLS deconvolution analysis divide into five statistically separable groups, which provide insight into regional trends in mineralogy.