Calibration of the Planetary Fourier Spectrometer long wavelength channel

The Planetary Fourier Spectrometer (PFS) experiment on board the Mars Express mission has two channels covering the 1.2-5 μm (SWC) and the 5-50 μm (LWC). The Long Wavelength Channel (LWC) measures the thermal emission spectrum of Mars between 200 and 2000 cm⁻¹ with a spectral resolution of 1.4 cm⁻¹, in absence of apodisation. We present here the calibration of this channel and its performance. The instrument calibration has been performed on ground, before launch, in space during Near Earth Verification (NEV) measurements, and at Mars. Special attention has been given to the problem of microvibrations on board the spacecraft.In order to obtain correct results, the source-instrument-detector interaction is studied very accurately. The instrument variations during a pericentre pass impose a complex procedure for the LW channel calibration, but fortunately the procedure adopted seems to work well. Samples of the calibrated data are given (as single spectrum and as an average over a few spectra) to show the performance of the experiment and its scientific potentialities.     

Calibration of the Planetary Fourier Spectrometer short wavelength channel

The Planetary Fourier Spectrometer (PFS) experiment on board the Mars Express mission has two channels covering the 1.2-5.5 μm short wavelength channel (SWC) and the 5.5-45 μm (LWC). The SWC measures part of the thermal emission spectrum and the solar reflected spectrum of Mars between 1700 and 8200 cm⁻¹ with a spectral resolution of 1.3 cm⁻¹, in absence of apodisation. We present here the calibration of this channel and its performance. The instrument calibration has been performed on ground, before launch, in space during near earth verification (NEV) measurements, and at Mars. Special attention has been given to the problem of microvibrations on board the spacecraft.In order to obtain correct results, the source-instrument-detector interaction for the thermal part is studied very accurately. The instrument shows a nonlinear behaviour with source intensity. The SNR increases with amplification, hence high gain factors are usually used. The detector is, in space, cooled by a passive radiator, and works around 210-215 K. The calibration source (an internal lamp) shows variations during a pericentre pass and therefore impose a complex procedure for the SW channel calibration. Mechanical microvibrations strongly affect part of the spectrum. We discuss the validity of the present calibration, and indicate possible future developments. Samples of the calibrated data are given to show the performance of the experiment and its scientific potentialities.     

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.     

Evidence for Mg-rich carbonates on Mars from a 3.9 μm absorption feature

The origin and nature of the early atmosphere of Mars is still debated. The discovery of sulfate deposits on the surface, coupled with the evidence that there are not large abundances of carbonates detectable on Mars in the optically accessible part of the regolith, leaves open different paleoclimatic evolutionary pathways. Even if carbonates are responsible for the feature observed by TES and Mini-TES at 6.76 μm, alternative hypotheses suggest that it could be due to the presence of Hydrated Iron Sulfates (HIS). Carbonates can be discerned from HIS by investigating the spectral region in which a strong overtone carbonate band is present. The Planetary Fourier Spectrometer on board the Mars Express spacecraft has acquired several thousand martian spectra in the range 1.2-45 μm since January 2004, most of which show a weak absorption feature between 3.8 and 4 μm. A similar feature was observed previously from the Earth, but its origin could not be straightforwardly ascribed to surface materials, and specifically to carbonates. Here we show the surficial nature of this band that can be ascribed to carbonate mixed with the martian soil materials. The materials that best reproduce the detected feature are Mg-rich carbonates (huntite [CaMg₃(CO₃)₄] and/or magnesite [MgCO₃]). The presence of carbonates is demonstrated in both bright and dark martian regions. An evaluation of the likeliest abundance gives an upper limit of ∼10 wt%. The widespread distribution of carbonates supports scenarios that suggest carbonate formation occurred not by precipitation in a water-rich environment but by weathering processes.     

Comparison of HIPWAC and Mars Express SPICAM observations of ozone on Mars 2006-2008 and variation from 1993 IRHS observations

Ozone is a tracer of photochemistry in the atmosphere of Mars and an observable used to test predictions of photochemical models. We present a comparison of retrieved ozone abundances on Mars using ground-based infrared heterodyne measurements by NASA Goddard Space Flight Center’s Heterodyne Instrument for Planetary Wind And Composition (HIPWAC) and space-based Mars Express Spectroscopy for the Investigation of the Characteristics of the Atmosphere of Mars (SPICAM) ultraviolet measurements. Ozone retrievals from simultaneous measurements in February 2008 were very consistent (0.8 μm-atm), as were measurements made close in time (ranging from <1 to >8 μm-atm) during this period and during opportunities in October 2006 and February 2007. The consistency of retrievals from the two different observational techniques supports combining the measurements for testing photochemistry-coupled general circulation models and for investigating variability over the long-term between spacecraft missions. Quantitative comparison with ground-based measurements by NASA/GSFC’s Infrared Heterodyne Spectrometer (IRHS) in 1993 reveals 2-4 times more ozone at low latitudes than in 2008 at the same season, and such variability was not evident over the shorter period of the Mars Express mission. This variability may be due to cloud activity.     

Martian atmospheric particulate spectral end-members recovery from PFS and IRIS data

We present an application of a multivariate analyses technique on data returned by the Planetary Fourier Spectrometer (PFS) instrument on board the ESA’s Mars Express (MEX) spacecraft in order to separate the atmospheric contribution from the observed radiation. We observe that Thermal/Far Infrared spectra returned from Mars, covering almost a whole martian year, can be represented by a linear model using a limited set of end-member spectra. We identify the end-members as the suspended mineral dust and water ice clouds, but no surface signature was found. We improve previous studies performed with data from the Thermal Emission Spectrometer (TES) thanks to the higher spectral resolution of PFS. This allows for distinguishing narrow gaseous bands present in the martian atmosphere. Furthermore, the comparison of results from PFS and TES with data collected in 1971 by the Mariner 9 Infrared Interferometer Spectrometer (IRIS) shows an atmospheric dust component with similar spectral behavior. This might indicate homogeneity of the dust source regions over a time period of more than 30 years.     

Mercury: Mid‐infrared (3–13.5 μm) observations show heterogeneous composition,presence of intermediate and basic soil types,and pyroxene

Abstract— The Aerospace Corporation's broadband array spectrograph system (BASS) mounted on the NASA infrared telescope facility (IRTF) on Mauna Kea, Hawaii was used to obtain spectral measurements of Mercury's thermal emission on 1998 March 21 (45–85° longitude), and on 1998 May 12 (68–108° longitude). The spectra show heterogeneous composition on Mercury's surface between longitudes 45–85° and about 68–108°. These observations include measurements from 3 to 6 μm, a spectral region not previously covered by mid‐infrared spectroscopy. Excellent quality data were obtained in the atmospheric windows between 3–4.2 and 4.6–5.5 μm. These wavelength regions exhibit high emissivity characteristic of a regolith with strong thermal gradients maintained in a vacuum environment with spectra dominated by grain sizes of ?30 μm. Emission peaks are present at 3.5 and 5 μm in the 45–85° longitude data. The 5 μm peak has been tentatively attributed to clinopyroxene. Data were also obtained in the 7.5–13.5 μm spectral region. Spectra obtained during both observing periods show well‐defined emissivity maxima (EM) in the spectral vicinity (between 7.7 and 9.2 μm) of the Christiansen frequency of silicate soils. The location of the EM for longitudes 45–85° (7.9 μm) is consistent with a surface composition of intermediate SiO₂ content. The overall spectral shape is similar to that obtained previously at the same location with different instrumentation. In the region 68–108° longitude, three EM are observed at 7.8, 8.2, and 9.2 μm, indicating the presence of distinctly different surface composition from the other location. Comparisons of these data to other mid‐infrared spectra of Mercury's surface and asteroids, and of the different instrumentation used in observations are included.     

Modelling of atmospheric dust extinction and surface reflectance of Mars applying a radiative transfer simulation in the 2.0 and 2.7 μm CO2 bands

Infrared radiation spectra of Mars which can be measured by an orbiting Planetary Fourier Spectrometer (PFS) have been simulated in the spectral region from 1 to 50 μm. The radiative transfer simulation technique considers absorption, emission and multiple scattering by molecular (CO₂, H₂O, CO) and particulate (palagonite) species. It is shown that the contribution from atmospheric dust extinction and surface reflectance can be separated in the region of the CO₂ bands at 2.0 and 2.7 μm. Quantitative results of simultaneous surface pressure, reflectance and aerosol optical depth retrievals are discussed.     

Spectral evidence of volcanic cryptodomes on the northern plains of Mars

The composition and detailed morphology of dome-shaped features located in western Arcadia Planitia and just west of Utopia Planitia were examined in this study utilizing data from Mars Reconnaissance Orbiter and Mars Odyssey sensors. The domes have diameters averaging 1.5 km and heights averaging 160 m, and are generally dark-toned, although some are lighter toned or have split dark and light-toned surfaces. The domes are surrounded by annular deposits comprising, with increasing distance from the domes, dark-toned aprons, light-toned aureoles, and dark-toned aureoles. Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) data over several areas in the western Arcadia region show that spectra from the flanks of several domes have 1 and 2 μm absorption features consistent with the presence of olivine and a high-Ca pyroxene, nominally augite. Modified Gaussian Model (MGM) analysis of these spectra indicates Fe-rich olivine compositions. The tops of domes and the aprons surrounding many domes have negative sloping flat spectra in the near infrared, which is consistent with tachylite-rich, glassy compositions. High Resolution Imaging Science Experiment (HiRISE) images over several domes indicate that relatively high thermal inertia values associated with the tops of domes can be attributed to boulder strewn surfaces. HiRISE images also reveal that light-toned aureoles around domes consist of crenulated ground resembling “brain terrain” textures previously described for ice-rich concentric crater fill elsewhere on the northern plains. The plains surrounding the domes also display lineations that are interpreted to be lava channels or tubes. The combination of volcanic and ice-related features are consistent with the domes having formed as cryptodomes in the near sub-surface. We suggest that the domes could be basaltic in composition if the magmas were degassed and/or highly crystallized, and thus more viscous than typical basaltic magmas. The intrusion of these magmas into an ice-rich horizon would have produced a pervasively jointed chilled margin on the domes, which, once the domes were exposed, would have mechanically weathered to form the dark aprons. The domes could have served as local centers for ice accumulation during periods of high orbital obliquity, which ultimately would have led to the formation of the “brain terrain” surrounding the features. The domes represent late stage volcanic products on the northern plains of Mars and associated features provide more evidence for the role that ice accumulation and modification has played in recent martian 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.     

Analysis of disturbances in the Planetary Fourier Spectrometer through numerical modeling

Fourier transform spectrometers are instruments with high sensitivity to many kinds of disturbances. This study started from the analysis of the disturbances related to mechanical vibrations on the PFS FTIR spectrometer to show how the measured spectra can differ from the actual ones. The complete study, more in general, accounts for the characteristics of a real instrument and its operating environment to show, which can be the effects of many sources of disturbances on realistic measurements. The analysis is especially relevant when the spectra are used for the determination of parameters through “best fitting techniques” by matching with synthetic ones because it shows how spectral features used in these studies can be modified by disturbances. A previous work addressed the theoretical treatment of vibrations borne effects on FTIR spectrometers and is the ground work for the present; however, that study, being based on an analytical approach could only show examples of single effects on simplified input signals such as emission lines. This study conversely is based on a numerical model, developed in order to include altogether the effects addressed in the theoretical work to show combined effects on complex spectra like those expected from Mars. This allows not only to evaluate the linked effects of many kinds of disturbances but also to account for the real spectrometer characteristics. The use of synthetic spectra as input allows the comparison between expected spectra and measured ones. The simulation is tailored on the Planetary Fourier Spectrometer (PFS), onboard the ESA Mars Express spacecraft, from 2003 orbiting around Mars and in particular on its short wavelength (SW) channel, where many disturbances are more evident.     

Potential for stratospheric Doppler windspeed measurements of Jupiter by sub-millimetre spectroscopy

The sub-millimetre/microwave range of the spectrum has been exploited in the field of Earth observation by many instruments over the years and has provided a plethora of information on atmospheric chemistry and dynamics—however, this spectral range has not been fully explored in planetary science, having been exclusively employed to carry out ground-based measurements. To this end, a sub-millimetre instrument, the Orbiter Terahertz Infrared Spectrometer (ORTIS), is studied by the University of Oxford and the Rutherford Appleton Laboratory, to meet the requirements of the European Space Agency's Cosmic Visions 2015-2025 programme—in particular, the Europa Jupiter System Mission (EJSM), which has the European Space Agency and the National Aeronautics and Space Administration as partners. ORTIS is designed to measure atmospheric temperature, the abundance of stratospheric water vapour and other jovian gases, and is intended to be capable of retrieving vertical profiles of horizontal windspeed in the stratosphere for the first time, from Doppler-shifted emission lines measured at high spectral resolution. In this work, a preliminary study and implementation of the estimation of windspeed profiles on simulated spectra representative of Jupiter is presented, detailing the development of the retrieval algorithm, showing that a sub-millimetre instrument such as ORTIS should be able to retrieve windspeed profiles to an accuracy of about 15 m/s between 70 and 200 km/0.1-10 mb using a single near-limb measurement, for expected noise amplitudes.     

Spectral emissivity measurements of Mercury's surface indicate Mg- and Ca-rich mineralogy, K-spar, Na-rich plagioclase, rutile, with possible perovskite, and garnet

Mid-infrared 2-D spectroscopic measurements from 8.0 to 12.7 μm of Mercury were taken using Boston University's Mid-Infrared Spectrometer and Imager (MIRSI) mounted on the NASA Infrared Telescope Facility (IRTF) on Mauna Kea, Hawaii, 7-11 April 2006. Measurements reported here cover radar bright region C, a dark plains region west of Caloris Basin, and the interior of Caloris Basin. By use of spectral deconvolution with a large spectral library composed of many mineral compositions and grain size separates, we fitted, or “unmixed”, the Mercury spectra. We find mineral suites composed of magnesium-rich orthopyroxene and olivine, Ca-, Mg-, Na-rich clinopyroxene, potassium feldspar, and Na-bearing plagioclase feldspar. Both Ca- and Mg-rich garnet (pyrope and grossular, respectively) are apparently present in small amounts. Opaque minerals are required for spectral matching, with rutile (TiO₂) repeatedly providing the “best fit”. However, in the case of the radar bright region C, perovskite also contributed to a very good fit. Caloris Basin infill is rich in both potassium feldspar and Na-rich plagioclase. There is little or no olivine in the Caloris interior smooth plains. Together with the high alkali content, this indicates that resurfacing magmas were low to intermediate in SiO₂. Data suggest the dark plains exterior to Caloris are highly differentiated low-iron basaltic magmas resulting in material that might be classified as oligoclase basalts.     

Composition and thermal inertia of the Mawrth Vallis region of Mars from TES and THEMIS data

Clay mineral-bearing deposits previously discovered on Mars with near infrared (λ=0.3-5 μm) remote sensing data are of major significance for understanding the aqueous history, geological evolution, and past habitability of Mars. In this study, we analyzed the thermal infrared (λ=6-35 μm) surface properties of the most extensive phyllosilicate deposit on Mars: the Mawrth Vallis area. Clay mineral-bearing units, which in visible images appear to be relatively light-toned, layered bedrock, have thermal inertia values ranging from 150 to 460 J m⁻² K⁻¹ s^−1/2. This suggests the deposits are composed of a mixture of rock with sand and dust at 100-meter scales. Dark-toned materials that mantle the clay-bearing surfaces have thermal inertia values ranging from 150 to 800, indicating variable degrees of rockiness or induration of this younger sedimentary or pyroclastic unit. Thermal Emission Spectrometer (TES) spectra of the light-toned rocks were analyzed with a number of techniques, but none of the results shows a large phyllosilicate component as has been detected in the same surfaces with near-infrared data. Instead, TES spectra of light-toned surfaces are best modeled by a combination of plagioclase feldspar, high-silica materials (similar to impure opaline silica or felsic glass), and zeolites. We propose three hypotheses for why the clay minerals are not apparent in thermal infrared data, including effects due to surface roughness, sub-pixel mixing of multiple surface temperatures, and low absolute mineral abundances combined with differences in spatial sampling between instruments. Zeolites modeled in TES spectra could be a previously unrecognized component of the alteration assemblage in the phyllosilicate-bearing rocks of the Mawrth Vallis area. TES spectral index mapping suggests that (Fe/Mg)-clays detected with near infrared data correspond to trioctahedral (Fe²⁺) clay minerals rather than nontronite-like clays. The average mineralogy and geologic context of these complex, interbedded deposits suggests they are either aqueous sedimentary rocks, altered pyroclastic deposits, or a combination of both.     

Effect of atmospheric dust loading on martian albedo measurements

This work is devoted to the analysis of the variation of albedo measured by orbiting instruments with atmospheric opacity on Mars. The study has been conduced by analysing Mars Global Surveyor Thermal Emission Spectrometer (MGS-TES) data from martian regions with different surface albedo.In support of these data, synthetic spectra with different surface albedo and atmospheric opacities have been computed, so that a comparison has been performed. The synthetic spectra have been retrieved by using two different grain sizes for suspended dust (0.5 and 1.2 μm), allowing a comparison between the two models and the observations.Using the DCI, a parameter describing the quantity of dust deposited on the surface, the effectiveness of the single scattering approximation has been tested for low atmospheric opacity by analysing the quality of the linear fit up to different atmospheric opacity.For more opaque conditions two kinds of fits have been applied to the data, linear and second-order degree polynomial. In this case, we found that the polynomial fit better describes the observations.The analysis of these data made it possible to notice a peculiar trend, already reported by Christensen (1988), of the albedo over Syrtis Major after the occurrence of dust storms, but, differently from that work, now the study of DCI together with atmospheric opacity and albedo allowed us to robustly confirm the hypothesis made by Christensen.Finally, the comparison between observations and synthetic spectra computed with models with different particles grain sizes indicates that dust particles of 0.5 μm diameter are the most effective to change the aerosol atmospheric opacity on Mars.     

Retrieval and tentative indentification of the 3 μm spectral feature in Titan's haze

Recently, an unidentified 3.3-3.4 μm feature found in the solar occultation spectra of the atmosphere of Titan observed by Cassini/VIMS was tentatively attributed to the C-H stretching mode of aliphatic hydrocarbon chains attached to large organic molecules, but without properly extracting the feature from adjacent influences of strong CH₄ and weak C₂H₆ absorptions (Bellucci et al., 2009). In this work, we retrieve the detailed spectral feature using a radiative transfer program including absorption and fluorescent emission of both molecules, as well as absorption and scattering by haze particles. The spectral features of the haze retrieved from the VIMS data at various altitudes are similar to each other, indicating relatively uniform spectral properties of the haze with altitude. However, slight deviations observed near 127 km and above 300 km suggest inhomogeneity at these altitudes. We find that the positions of the major spectral peaks occur at 3.33-3.37 μm, which are somewhat different from the typical 3.3 μm aromatic or 3.4 μm aliphatic C-H stretches usually seen in the spectra of dust particles of the interstellar medium and comets. The peaks, however, coincide with those of the solid state spectra of C₂H₆, CH₄, and CH₃CN; and a broad shoulder from 3.37 to 3.50 μm coincides with those of C₅H₁₂ and C₆H₁₂ as well as those of typical aliphatic C-H stretches. This result combined with high-altitude (∼1000 km) haze formation process recently reported by Waite et al. (2007) opens a new question on the chemical composition of the haze particles. We discuss the possibility that the 3 μm feature may be due to the solid state absorption bands of these molecules (or some other molecules) and we advocate additional laboratory measurements for the ices of hydrocarbon and nitrogen-bearing molecules present in Titan's atmosphere for the identification of this 3 μm feature.     

Principal components analysis of Mars in the near-infrared

Principal components analysis and target transformation are applied to near-infrared image cubes of Mars in a study to disentangle the spectra into a small number of spectral endmembers and characterize the spectral information. The image cubes are ground-based telescopic data from the NASA Infrared Telescope Facility during the 1995 and 1999 near-aphelion oppositions when ice clouds were plentiful [ [Clancy et al., 1996] and [56]], and the 2003 near-perihelion opposition when ice clouds are generally limited to topographically high regions (volcano cap clouds) but airborne dust is more common [Martin, L.J., Zurek, R.W., 1993. J. Geophys. Res. 98 (E2), 3221-3246]. The heart of the technique is to transform the data into a vector space along the dimensions of greatest spectral variance and then choose endmembers based on these new “trait” dimensions. This is done through a target transformation technique, comparing linear combinations of the principal components to a mineral spectral library. In general Mars can be modeled, on the whole, with only three spectral endmembers which account for almost 99% of the data variance. This is similar to results in the thermal infrared with Mars Global Surveyor Thermal Emission Spectrometer data [Bandfield, J.L., Hamilton, V.E., Christensen, P.R., 2000. Science 287, 1626-1630]. The globally recovered surface endmembers can be used as inputs to radiative transfer modeling in order to measure ice abundance in martian clouds [Klassen, D.R., Bell III, J.F., 2002. Bull. Am. Astron. Soc. 34, 865] and a preliminary test of this technique is also presented.     

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.     

Interferometric millimeter observations of water vapor on Mars and comparison with Mars Express measurements

We present interferometric mapping of the 225.9-GHz HDO and 203.4-GHz lines on Mars obtained with the IRAM Plateau de Bure facility (PdBI). The observations were performed during martian year 28 (MY28), at L_s=320.3° for the HDO line, and at L_s=324.3° for the line. The HDO line is detected at the eastern (morning) and western (evening) limbs of the northern hemisphere, corresponding to a water column density in the range 3-6 pr.-μm. The line is not detected, which is compatible with the column densities derived from the HDO line. Quasi-simultaneous far infrared measurements obtained by the Planetary Fourier Spectrometer (PFS) onboard the Mars Express spacecraft confirm our PdBI results, yielding a 5±1 pr.-μm meridionally constant water column abundance.Such a low water abundance during the southern mid-autumn of MY28 does not correspond to the standard martian climatology as observed during the previous years. It was however already retrieved from near-infrared observations performed by the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) onboard the Mars Reconnaissance Orbiter spacecraft [Smith, M.D., Wolff, M.J., Clancy, R.T., Murchie, S.L. 2009. CRISM observations of water vapor and carbon monoxide. J. Geophys. Res. 114, doi: 10.1029/2008JE003288]. Our observations thus confirm that the planet-encircling dust storm that occurred during MY28 significantly affected the martian water cycle. Our observations also demonstrate the usefulness of interferometric submillimeter observations to survey the martian water cycle from ground-based facilities.