Spectral reflectance properties of carbonates from terrestrial analogue environments: Implications for Mars

Spectroscopic analysis of carbonate-bearing samples from a variety of terrestrial environments provides important insights into spectroscopy-based investigations of Mars designed to detect the presence of carbonate minerals. In order to better address the spectral detectability of carbonates on Mars, we examined the spectral reflectance properties of carbonates and carbonate-bearing lithologies from a variety of terrestrial environments, including impact structures (Haughton, St. Martin, Eagle Butte), landslides (Frank), quarrying operations (Hecla), carbonates affected by weathering (Haughton, East German Creek), and sulfide-sulfate-carbonate assemblages (Central Manitoba). The goal is to identify processes and environments that can affect spectroscopy-based carbonate detection, for more detailed follow-on studies. Common carbonates appear to be stable, from a spectroscopic perspective, to various tectonic processes. Iron oxides/hydroxides do not appear to significantly affect spectral detectability of carbonates, as the spectrum-altering effects of these phases are largely restricted to the region below ∼1 μm, while useful carbonate absorption bands occur longward of ∼1.8 μm. Carbonate detection and characterization in the 0.35-2.5-μm region is largely restricted to a single absorption feature in the 2.3-μm region, which can be problematic for robust carbonate identification. While tectonic processes and iron oxide/hydroxide staining do not appear to significantly impair carbonate detection based on the 2.3-μm region absorption band, a number of other factors can affect carbonate detection. These include the fact that this absorption band is weak compared to many other minerals, a number of other minerals also exhibit absorption bands in this wavelength region (leading to possible misidentifications), and that even small abundances of minerals that absorb strongly in this region will reduce the strength of the carbonate absorption band. Identifying the nature of accessory minerals associated with carbonates can be used to constrain possible formation environments. Ongoing research at carbonate-bearing terrestrial analogue sites will continue to provide new insights into the occurrence and detection of carbonates on Mars.     

Spectral detectability of Ca- and Mg-sulfates in Martian bright soils in the 4–5 μm wavelength range

Chemical analyses of soil samples performed at different landing sites on Mars suggest the presence of sulfate minerals. These minerals are also thought to be present in the globally mixed Martian bright soils covering large areas of the planet. However, remote soil spectra have so far provided only tentative identification of sulfates regarding mineral types and abundances. This paper concentrates on the detectability of four Ca- and Mg-sulfates (anhydrite, gypsum, kieserite, hexahydrite) in the 4–5 μm range of Martian remote soil spectra. This spectral range is important for sulfate detection as most fine-grained sulfates exhibit significant absorption bands between 4 and 5 μm, independent of the texture of the host soils (e.g., loose powdered or cemented soils). Furthermore, this is the spectral range for which the Planetary Fourier Spectrometer (PFS) and Observatoire pour la Minéralogie, l’Eau, les Glaces, et l’Activité (OMEGA) instruments onboard ESA/Mars Express mission provide high spectral and spatial resolution data. Laboratory near- and mid-IR reflectance spectra of the pure sulfates and their mixtures with a terrestrial Martian soil analog were acquired. The results show that even the smallest amount of admixed sulfate (∼5 wt%) generates significant absorption features in the portion of the 4–5 μm range not covered by the saturated Martian atmospheric CO₂ absorption band between 4.2 and 4.4 μm. Model calculations of the influence of emitted surface radiation on the detectability of sulfate features show that the depth of the features decreases strongly with increasing surface temperature of an observed area resulting in the fact that all sulfates are spectrally hidden at surface temperatures around 270 K even at ∼14 or ∼25 wt% sulfate content in the soils. Sulfates become increasingly detectable depending on the sulfate content if the surface temperature is below 260 K. The outcome of this work helps to constrain the conditions needed for remote detection of sulfates within Martian bright soils in the 4–5 μm range.     

Morphology, stratigraphy, and mineralogical composition of a layered formation covering the plateaus around Valles Marineris, Mars: Implications for its geological history

An extensive layered formation covers the high plateaus around Valles Marineris. Mapping based on HiRISE, CTX and HRSC images reveals these layered deposits (LDs) crop out north of Tithonium Chasma, south of Ius Chasma, around West Candor Chasma, and southwest of Juventae Chasma and Ganges Chasma. The estimated area covered by LDs is ∼42,300 km². They consist of a series of alternating light and dark beds, a 100 m in total thickness that is covered by a dark unconsolidated mantle possibly resulting from their erosion. Their stratigraphic relationships with the plateaus and the Valles Marineris chasmata indicate that the LDs were deposited during the Early- to Late Hesperian, and possibly later depending on the region, before the end of the backwasting of the walls near Juventae Chasma, and probably before Louros Valles sapping near Ius Chasma. Their large spatial coverage and their location mainly on highly elevated plateaus lead us to conclude that LDs correspond to airfall dust and/or volcanic ash. The surface of LDs is characterized by various morphological features, including lobate ejecta and pedestal craters, polygonal fractures, valleys and sinuous ridges, and a pitted surface, which are all consistent with liquid water and/or water ice filling the pores of LDs. LDs were episodically eroded by fluvial processes and were possibly modified by sublimation processes. Considering that LDs correspond to dust and/or ash possibly mixed with ice particles in the past, LDs may be compared to Dissected Mantle Terrains currently observed in mid- to high latitudes on Mars, which correspond to a mantle of mixed dust and ice that is partially or totally dissected by sublimation. The analysis of CRISM and OMEGA hyperspectral data indicates that the basal layer of LDs near Ganges Chasma exhibits spectra with absorption bands at ∼1.4 μm, and ∼1.9 μm and a large deep band between ∼2.21 and ∼2.26 μm that are consistent with previous spectral analysis in other regions of LDs. We interpret these spectral characteristics as an enrichment of LDs in opaline silica or by Al-phyllosilicate-rich layers being overlain by hydroxylated ferric sulfate-rich layers. These alteration minerals are consistent with the aqueous alteration of LDs at low temperatures.     

The 1.7- to 4.2-μm spectrum of asteroid 1 Ceres: Evidence for structural water in clay minerals

A high-resolution Fourier spectrum (1.7–3.5 μm) and medium-resolution spectrophotometry (2.7–4.2 μm) were obtained for Asteroid 1 Ceres. The presence of the 3-μm absorption feature due to water of hydration was confirmed. The 3-μm feature is compared with the 3-μm bands due to water of hydration in clays and salts. It is concluded that the spectrum of Ceres shows a strong absorption at 2.7–2.8 μm due to structural OH groups in clay minerals. The dominant minerals on the surface of Ceres are therefore hydrated clay minerals structurally similar to terrestrial montmorillonites. There is also a narrow absorption feature at 3.1 μm which is attributable to a very small amount of water ice on Ceres. This is the first evidence for ice on the surface of an asteroid.     

Evidence for frost on Rhea's surface

We have observed Rhea (S5) at 1.6 μm and 2.2 μm at Mt. Wilson using the Caltech photometer on the 1.52m and 2.54m telescopes. The infrared spectral reflectances relative to 0.55μm are 0.8 (±0.1 p.e.) at 1.65μm and 0.6 (±0.1 p.e.) at 2.2μm. Such absorption bands in the near infrared are not consistent with spectra of most rocks or minerals; even carbonaceous chondritic materials have nearly flat reflectances over this spectral region. Frosts, however, have strong absorption bands in the 1–3μm region. In particular, the broadband infrared reflectances of Rhea are similar to those of the Galilean satellites Europa (J2) and Ganymede (J3) and also the rings of Saturn (all of which are known from high resolution scans to have water frosts on their surfaces). The broadband photometry does not have sufficient resolution to identify the frost species: but Rhea's low density, high albedo and relatively flat reflectance from 0.3μm to 1.1μm as well as the low infrared reflectances reported here are consistent with the presence of water ice on Rhea's surface.     

Saturn’s F ring grains: Aggregates made of crystalline water ice

We present models of the near-infrared (1-5 μm) spectra of Saturn’s F ring obtained by Cassini’s Visual and Infrared Mapping Spectrometer (VIMS) at ultra-high phase angles (177.4-178.5°). Modeling this spectrum constrains the size distribution, composition, and structure of F ring particles in the 0.1-100 μm size range. These spectra are very different from those obtained at lower phase angles; they lack the familiar 1.5 and 2 μm absorption bands, and the expected 3 μm water ice primary absorption appears as an unusually narrow dip at 2.87 μm. We have modeled these data using multiple approaches. First, we use a simple Mie scattering model to constrain the size distribution and composition of the particles. The Mie model allows us to understand the overall shapes of the spectra in terms of dominance by diffraction at these ultra-high phase angles, and also to demonstrate that the 2.87 μm dip is associated with the Christiansen frequency of water ice (where the real refractive index passes unity). Second, we use a combination of Mie scattering with Effective Medium Theory to probe the effect of porous (but structureless) particles on the overall shape of the spectrum and depth of the 2.87 μm band. Such simple models are not able to capture the shape of this absorption feature well. Finally, we model each particle as an aggregate of discrete monomers, using the Discrete Dipole Approximation (DDA) model, and find a better fit for the depth of the 2.87 μm feature. The DDA models imply a slightly different overall size distribution. We present a simple heuristic model which explains the differences between the Mie and DDA model results. We conclude that the F ring contains aggregate particles with a size distribution that is distinctly narrower than a typical power law, and that the particles are predominantly crystalline water ice.     

The influence of van der Waals forces on the state of water in the shallow subsurface of Mars

Microscopic liquid layers of water can evolve via adsorption on grain and mineral surfaces at and in the soil of the surface of Mars. The upper parts of these layers will start to freeze at temperatures clearly below the freezing point of bulk water (freezing point depression). A sandwich structure with layers of ice (top), liquid water (in between) and mineral surface (bottom) can evolve. The properties of the interfacial water (of adsorption water and premelted ice) on grain surfaces are described by a sandwich-model of a layer of liquid-like adsorption water between the adsorbing mineral surface layer and an upper ice layer. It is shown that the thickness or number of mono-layers of the interfacial water (of adsorption water and premelted ice) depends on temperature and atmospheric relative humidity. The derived equations for the sandwich model fit well to a known phenomenological relation between thickness of the liquid layer and relative humidity, and can be a tool to estimate or to determine for appropriate materials Hamaker's constant for van der Waals interactions on grains and in porous media. The curvature of grain surfaces is shown to have no remarkable effects for particles in the μm-range and larger. The application of these equations to thermo-physical conditions on Mars shows that the thickness of frost-layers, which can evolve over several hours on cooling surface parts of Mars, is typically of the order or a few tenths of one millimeter or less. This is in agreement with observations. Furthermore, an equation is derived, which relates the freezing point depression for van der Waals force governed interfacial water to the value of the Hamaker constant, to the latent heat of solidification, to the mass density of water ice, and to the thickness of the liquid-like layer. Again, this equation fits well to a known phenomenological relation between freezing point depression and thickness of the liquid-like layer. The derived equation shows that the lower limiting temperature of the liquid phase can reach about 180 K under martian conditions having an atmospheric water content of around 10 pr μm. An “Equilibrium Moisture Content” (EMC)/“Equilibrium Relative Humidity” (ERH) relation for the water content of martian soil has been derived, which relates, for equilibrium conditions, soil water content and atmospheric relative humidity. This relation indicates that the content of liquid interfacial water in the upper surface of Mars can reach up to 10% by weight and more in course of saturation during night hours, and it can be of about 2% by weight during the dry daytime hours.     

Observations of water vapour and carbon monoxide in the Martian atmosphere with the SWC of PFS/MEX

In the history of Mars exploration its atmosphere and planetary climatology aroused particular interest. In the study of the minor gases abundance in the Martian atmosphere, water vapour became especially important, both because it is the most variable trace gas, and because it is involved in several processes characterizing the planetary atmosphere. The water vapour photolysis regulates the Martian atmosphere photochemistry, and so it is strictly related to carbon monoxide. The CO study is very important for the so-called “atmosphere stability problem”, solved by the theoretical modelling involving photochemical reactions in which the H₂O and the CO gases are main characters.The Planetary Fourier Spectrometer (PFS) on board the ESA Mars Express (MEX) mission can probe the Mars atmosphere in the infrared spectral range between 200 and 2000 cm^?1 (5–50 μm) with the Long Wavelength Channel (LWC) and between 1700 and 8000 cm^?1 (1.2–5.8 μm) with the Short Wavelength Channel (SWC). Although there are several H₂O and CO absorption bands in the spectral range covered by PFS, we used the 3845 cm^?1 (2.6 μm) and the 4235 cm^?1 (2.36 μm) bands for the analysis of water vapour and carbon monoxide, respectively, because these ranges are less affected by instrumental problems than the other ones. The gaseous concentrations are retrieved by using an algorithm developed for this purpose.The PFS/SW dataset used in this work covers more than two and a half Martian years from Ls=62° of MY 27 (orbit 634) to Ls=203° of MY 29 (orbit 6537). We measured a mean column density of water vapour of about 9.6 pr. μm and a mean mixing ratio of carbon monoxide of about 990 ppm, but with strong seasonal variations at high latitudes. The seasonal water vapour map reproduces very well the known seasonal water cycle. In the northern summer, water vapour and CO show a good anticorrelation most of the time. This behaviour is due to the carbon dioxide and water sublimation from the north polar ice cap, which dilutes non-condensable species including carbon monoxide. An analogous process takes place during the winter polar cap, but in this case the condensation of carbon dioxide and water vapour causes an increase of the concentration of non-condensable species. Finally, the results show the seasonal variation of the carbon monoxide mixing ratio with the surface pressure.     

Measurements of water vapor in Mars' Antarctic

A complete Mars year of measurements of atmospheric water vapor in the south arctic have been obtained from the Viking Orbiters. Analysis of the observations indicates that, except for the south remnant cap, the southern hemisphere of Mars is devoid of any substantial reservoirs of water in contact with the atmosphere, and that, in the summer time, the top layer of soil is desiccated. Small amounts of water ice are incorporated into the annual CO₂ cap; this water is released at the cap margin when it retreats in the spring. The first global dust storm resulted in heating of the south arctic atmosphere and a transport of water in from the equatorial region. The second global dust storm had a negligible effect on atmospheric water vapor; the dust contained little water.     

An improvement to the volcano-scan algorithm for atmospheric correction of CRISM and OMEGA spectral data

The observations of Mars by the CRISM and OMEGA hyperspectral imaging spectrometers require correction for photometric, atmospheric and thermal effects prior to the interpretation of possible mineralogical features in the spectra. Here, we report on a simple, yet non-trivial, adaptation to the commonly-used volcano-scan correction technique for atmospheric CO₂, which allows for the improved detection of minerals with intrinsic absorption bands at wavelengths between 1.9 and 2.1 μm. This volcano-scan technique removes the absorption bands of CO₂ by ensuring that the Lambert albedo is the same at two wavelengths: 1.890 and 2.011 μm, with the first wavelength outside the CO₂ gas bands and the second wavelength deep inside the CO₂ gas bands. Our adaptation to the volcano-scan technique moves the first wavelength from 1.890 μm to be instead within the gas bands at 1.980 μm, and for CRISM data, our adaptation shifts the second wavelength slightly, to 2.007 μm. We also report on our efforts to account for a slight ∼0.001 μm shift in wavelengths due to thermal effects in the CRISM instrument.     

The rings of Saturn: New near-infrared reflectance measurements and a 0.326–4.08 μm summary

A new high photometric precision reflectance spectrum of Saturn's rings covering the spectral region 0.65 to 2.5-μm is presented and three previously unreported absorption features at 1.25, 0.85, and probably 1.04 μm are identified. The 1.25- and 1.04-μm absorptions are due to water ice. The 0.85-μm feature may be due to a combination of 0.81- and 0.90-μm ice absorptions but this feature appears too strong relative to the 1.04-μm band to be completely explained by weater ice. Another possibility is that the 0.85-μm band is due to Fe³⁺-bearing minerals in an ice-mineral mixture. This explanation could also account for the drop in the visible and ultraviolet reflectance and the rise in reflectance around 3.6 μm. Finally, a composite spectrum from 0.325 to 4.08 μm is presented which will be useful for future analysis and laboratory studies.     

Evidence for enhanced hydration on the northern flank of Olympus Mons, Mars

In this paper we report about a small region on the northern scarp of Olympus Mons showing an increase of the 3 μm hydration band in the OMEGA spectra, together with low superficial temperatures. Although water ice clouds can occurs on the flank of big martian volcanoes, radiative transfer modeling indicates that atmospheric water ice alone cannot justify the shape of the observed band. A fit of the 1.9–3 μm absorption features is obtained by hypothesizing that the study region consists of a mixture of dust and water ice covered by an optically thin (τ=0.08 at 3 μm) layer of dust. Thermal modeling also suggests that water ice in this region may be stable during most of the martian year due to the saturation of the atmosphere. If water ice is responsible for the observed spectral behavior, it might consist of a number of ice or snow patches possibly deposited in small depressions.     

Saturn's satellites: Nuar-infrared spectrophotometry (0.6–2.5 μm) of the leading and trailing sides and compositional implications

Near-infrared spectra, 0.65–2.5 μm, are presented for Tethys, Dione, Rhea, Iapetus, and Hyperion. Water ice absorptions at 2.0, 1.5, and 1.25 μm are seen in the spectra of all five objects (except the 1.25-μm band was not detected in spectra of Hyperion) and the weak 1.04-μm ice absorption is detected on the leading and trailing sides of Rhea, and the trailing side of Dione. Upper limits to the 1.04-μm ice band depth are <0.3% for the leading side of Dione; <0.7% for the leading side of Iapetus, and the trailing side of Tethys; <1% on the trailing side of Iapetus; and <5% on the leading side of Tethys. The leading-trailing side ice band depth differences on Saturn's satellites are similar to those for the Galilean satellites, indicating possible surface modification by magnetospheric charged particle bombardment. Limits are determined for the amount of particulates, trapped gases, and amonium hydroxide on the surface. The surfaces of Saturn's satellites (except the dark side of Iapetus) are nearly pure water ice, with probably less than about 1 wt% particulate minerals. The ice could be clathrates with as much as a few weight percent trapped gases. The upper limit of amonium hydroxide depends on the spectral data precision and varies from ～ 1 wt% NH₃ for the leading side of Rhea to ～ 10 wt% NH₃ for Dione.     

The Galilean satellites: New near-infrared spectral reflectance measurements (0.65–2.5 μm) and a 0.325–5 μm summary

New near-infrared (0.65–2.5 μm) reflectance spectra of the Galilean satellites with 1.5% spectral resolution and ≈2% intensity precision are presented. These spectra more precisely define the water ice absorption features previously identified on Europa, Ganymede, and Callisto at 1.55 and 2.0 μm. In addition, previously unreported spectral features due to water ice are seen at 1.25, 1.06, 0.90, and 0.81 μm on Europa, and at 1.25, 1.04, and possibly 0.71 μm on Ganymede. Unreported absorption features in Callisto's spectrum occur at 1.2 μm, probably due to H₂O, and a weak, broad band extending from 0.75 to 0.95 μm, due possibly to other minerals. The spectrum of Io has only weak absorption features at 1.15 μm and between 0.8 and 1.0 μm. No water absorptions are positively identified in the Io spectra, indicating an upper limit of areal water frost coverage of 2% (leading and trailing sides). It is found for Callisto, Ganymede, and Europa that the water ice absorption features are due to free water and not to water bound or absorbed onto minerals. The areal coverage of water frost is ≈ 100% on Europa (trailing side), ≈65% on Ganymede (leading side), and 20–30% on Callisto (leading side). An upper limit of ≈5% bound water (in addition to the 20–30% ice) may be present on Callisto, based on the strong 3-μm band seen by other investigators. A summary of spectra of the satellites from 0.325 to about 5 μm to aid in laboratory and interpretation studies is also presented.     

Spectral imaging of martian water ice clouds and their diurnal behavior during the 1999 aphelion season (Ls = 130°)

We report high-spectral-resolution (λ/δλ = 800-2300) near-infrared mapping observations of Mars at L_s = 130° (April 1999), which were obtained by drift-scanning the cryogenic long-slit spectrometer at the KPNO 2.2-m telescope across the disk. Data were reformatted into calibrated spectral image cubes (x,y,λ) spanning 2.19 to 4.12 μm, which distinguish atmospheric CO₂ features, solar lines, and surface and aerosol features. Maps of relative band depth between 3.0 and 3.5 μm trace water ice clouds and show the diurnal evolution of features in the persistent northern summer aphelion cloud belt, which was mapped contemporaneously but at fixed local time by the Mars Global Surveyor Thermal Emission Spectrometer (MGS/TES). Cloud optical depth, particle sizes, and ice aerosol content were estimated using a two-stream, single-layer scattering model, with Mie coefficients derived from recently published ice optical constants, followed by a linear spectral deconvolution process. A comparison of data and model spectra shows evaporating nighttime clouds in the morning followed by afternoon growth of a prominent orographic cloud feature on the west flank of Elysium Mons. Cloud optical depth at 3.2 μm evolved to 0.28 ± 0.13 and ice aerosol column abundance to 0.9 ± 0.3 pr μm in the afternoon. Column abundances as large as 0.17 pr μm were retrieved in nonorographic clouds within the aphelion cloud band around midday. These clouds exhibit a modest decline in optical depth during the afternoon. Results show that ice particle radii from <2 μm to >4 μm exist in both cloud types. However, large particles dominate the spectra, consistent with recent MGS/TES emission phase function measurements of aphelion cloud aerosol properties.     

Spatial inhomogeneity of the martian subsurface water distribution: implication from a global water cycle model

In an effort to test and to understand the global hydrogen distribution in the shallow subsurface of Mars retrieved by the Mars Odyssey gamma-ray spectrometer, the present state and movement of water are investigated by a coupled global subsurface-atmosphere water cycle model. It was found that the observed global subsurface hydrogen distribution is largely consistent with the modeled global water cycle, so a large fraction of hydrogen is likely to exist as water, at low and mid latitudes in the form of adsorbed water. Under the present climate the water content in the shallow subsurface becomes higher in the northern hemisphere than in the southern hemisphere as a result of global water cycle, regardless of the initial water distribution in the soil or adsorptive capacity. The higher annual maximum soil temperature in the south, stronger net northward transport of atmospheric water vapor, and the emission of vapor from the northern residual polar cap in northern summer contribute to this hemispheric asymmetry. The generally higher adsorptive capacity of clay minerals in the northern plains may further increase this bias. The longitudinal inhomogeneity is caused by several factors, such as thermal inertia, adsorptive capacity, and atmospheric surface pressure. The water abundance is locally high in low thermal inertia regions (e.g., Arabia Terra) and at deep places where the surface pressure is high (e.g., Hellas); it is low in soil with a low adsorptive capacity (e.g., Tharsis) and high thermal inertia regions (e.g., Solis Planum). Most of the soil humidity near the surface at low and mid latitudes may originate from the atmosphere. The model implies that the upper soil layer should be largely ice-free because otherwise an excessive sublimation and vapor emission into the atmosphere in warm seasons would violate the observational constraints. Moreover, the more uniform latitudinal variation of the observed hydrogen abundance near the surface compared to that of deeper layers is indicative of the presence of adsorbed water instead of ground ice because the adsorbed water content does not as steeply depend on latitude as the ground ice stability. Concerning the regolith mineralogy, montmorillonite can much better account for the observed water cycle than palagonite. While the presence of permanent ground ice appears likely in the polar region below a thin layer, large seasonal cycle of phase change between pore ice and adsorbed water may be possible. Regolith adsorption/desorption is neither negligible nor crucial for the seasonal atmospheric water cycle, but the surface-atmosphere coupling is a major prerequisite for the long-term evolution of subsurface water distribution.     

Seasonal redistribution of water in the surficial Martian regolith: Results from the <Emphasis Type="Italic">Mars Odyssey</Emphasis> high-energy neutron detector (HEND)

The seasonal variation of neutron emissions from Mars in different spectral intervals measured by the HEND neutron detector for the entire Martian year are analyzed. Based on these data, the spatial variations of the neutron emissions from the planet are globally mapped as a function of season, and the dynamics of seasonal variation of neutron fluxes with different energies is analyzed in detail. No differences were found between seasonal regimes of neutron fluxes in different energy ranges in the southern hemisphere of Mars, while the regime of fast neutrons (with higher energies) during the northern winter strongly differs from that during the southern winter. In winter (L _s = 270°–330°), the fast neutron fluxes are noticeably reduced in the northern hemisphere (along with the consecutive thickening of the seasonal cap of solid carbon dioxide). This provides evidence of a temporary increase in the water content in the effective layer of neutron generation. According to the obtained estimates, the observed reduction of the flux of fast neutrons in the effective layer corresponds to an increase in the water abundance of up to 5% in the seasonal polar cap (70°–90°N), about 3% at mid-latitudes, and from 1.5 to 2% at low latitudes. The freezing out of atmospheric water at the planetary surface (at middle and high latitudes) and the hydration of salt minerals composing the Martian soil are considered as the main processes responsible for the temporary increase in the water content in the soil and upper layer of the seasonal polar cap. The meridional atmospheric transport of water vapor from the summer southern to the winter northern hemisphere within the Hadley circulation cell is a basic process that delivers water to the subsurface soil layer and ensures the observed scale of the seasonal increase in water abundance. In the summer northern hemisphere, the similar Hadley circulation cell transports mainly dry air masses to the winter southern hemisphere. The point is that the water vapor becomes saturated at lower heights during aphelion, and the bulk of the atmospheric water mass is captured in the near-equatorial cloudy belt and, thus, is only weakly transferred to the southern hemisphere. This phenomenon, known as the Clancy effect, was suggested by Clancy et al. (1996) as a basic mechanism for the explanation of the interhemispheric asymmetry of water storage in permanent polar caps. The asymmetry of seasonal meridional circulation of the Martian atmosphere seems to be another factor determining the asymmetry of the seasonal water redistribution in the “atmosphere-regolith-seasonal polar caps” system, found in the peculiarities of the seasonal regime of the neutron emission of Mars.     

Spectroscopy of Mars from 2.04 to 2.44 micrometers during the 1993 opposition: absolute calibration and atmospheric vs mineralogic origin of narrow absorption features

We present moderate-resolution (lambda/delta lambda = 300 to 370) reflectance spectra of Mars from 2.04 to 2.44 micrometers that were obtained at UKIRT during the 1993 opposition. Seven narrow absorption features were detected and found to have a Mars origin. By comparison with solar and Mars atmospheric spectra, five of these features were attributed all or in part to Mars atmospheric CO2 or CO(2.052 +/- 0.003, 2.114 +/- 0.002, 2.150 +/- 0.003, 2.331 +/- 0.001, and 2.357 +/- 0.002 micrometers). Two of the bands (2.331 +/- 0.001 and 2.357 +/- 0.002 micrometers) appear to have widths and depths that are consistent with additional, nonatmospheric absorptions, although a solar contribution cannot be entirely ruled out. Two other weak bands centered at 2.278 +/- 0.002 and 2.296 +/- 0.002 micrometers may be at least partially mineralogic in origin. The data provide no conclusive identification of the mineralogy responsible for these absorption features. However, examination of terrestrial spectral libraries and previous moderate spectral resolution mineral studies indicates that the most likely origin of these features is either (bi)carbonate or (bi)sulfate anions in framework silicates or (Fe, Mg)-OH bonds in sheet silicates. If the bands are caused by phyllosilicate minerals, then an explanation must be found for the extremely narrow widths of the cation-OH features in the Mars spectra as compared to terrestrial minerals.     

Mapping of water frost and ice at low latitudes on Mars

This paper reports on mapping of water frost and ice on Mars, in the range of latitudes between 30°S and 30°N. The study has been carried out by analysing 2485 orbits acquired during almost one martian year by the Mars Express/OMEGA imaging spectrometer. Water frost/ice is identified by the presence of ∼1.5 μm, ∼2 μm and ∼3.0 μm absorptions. Although the orbits analysed in this study cover all seasons, water frost/ice is observed only near the aphelion seasons, at Ls = 19° and at Ls = 98-150°. Water frost/ice is detected mainly on the southern hemisphere between 15°S and 30°S latitude while it has not been identified within 15°S-15°N. In the northern hemisphere, the water frost/ice detection is complicated by the presence of clouds. Usually, water frost/ice is found in shadowed areas, while in few cases it is exposed to the sunlight. This indicates a clear relationship with the local illumination conditions on the slopes which favour the water frost/ice deposition on the surface when the temperatures are very low. OMEGA observations span from 10 to 17 LT and the frost/ice is detected mainly between 15 and 16 LT, with practically no detection before 13 LT. We think this is due to the fact that the 10-12 LT observations occur at large distances and it is not a local time effect. A thermal model is used to determine the deposition conditions on the sloped surfaces where water frost/ice has been found. There, daily atmospheric saturation does not occur on pole facing 10-25° slopes with current water vapour abundances but only by assuming values greater than 40 pr μm. Moreover, the water frost/ice is not detected during the northern winter, even if the thermal model foresees daily saturation on 25° slopes.     

Investigation of water signatures at gully-exposed sites on Mars by hyperspectral image analysis

High-resolution images from the Mars Obiter Camera (MOC) onboard the Mars Global Surveyor (MGS) show a variety of gully features on sloped surfaces of Mars. The mechanism of gully formation is still under debate, although a majority of studies tend to favor a mechanism related to liquid water flow based on geomorphology and fluid mechanics considerations. In this study, we examined four known gully sites using Visible and Infrared Mineralogical Mapping Spectrometer (OMEGA) imagery. In particular, we analyzed the absorption depths of the water-associated absorption bands and concluded that there are stronger water signatures at the gully-exposed sites than in the surrounding areas. This implies that the water signatures, most likely representing water ice, isolated water molecules, and/or hydroxyl molecules incorporated into minerals, are still present in the shallow unconsolidated soils. This study provides additional evidence that water was likely involved in the formation of the gully features and is still locally active on the Martian surface in the present time.