Ultraviolet complex refractive index of Martian dust: Laboratory measurements of terrestrial analogs

The optical complex index of refraction of four candidate Martian surface materials has been determined between 0.185 and 0.4 μm using a modified Kubelka-Munk scattering theory. The candidate materials were limonite, andesite, montmorillonite, and basalt. The effect of scattering has been removed from the results. Also presented are diffuse reflection and transmission data on these samples.     

Evaporation of ice in planetary atmospheres: Ice-covered rivers on mars

The evaporation rate of water ice on the surface of a planet with an atmosphere involves an equilibrium between solar heating and radiative and evaporative cooling of the ice layer. The thickness of the ice is governed principally by the solar flux which penetrates the ice layer and then is conducted back to the surface. These calculations differ from those of Lingenfelter et al. [(1968) Science161, 266–269] for putative lunar channels in including the effect of the atmosphere. Evaporation from the surface is governed by two physical phenomena: wind and free convection. In the former case, water vapor diffuses from the surface of the ice through a lamonar boundary layer and then is carried away by eddy diffusion above, provided by the wind. The latter case, in the absence of wind, is similar, except that the eddy diffusion is caused by the lower density of water vapor than the Martian atmosphere. For mean Martian insolations the evaporation rate above the ice is ～ 10^?8 g cm^?2 sec^?1. Thus, even under present Martian conditions a flowing channel of liquid water will be covered with ice which evaporates sufficiently slowly that the water below can flow for hundreds of kilometers even with quite modest discharges. Evaporation rates are calculated for a wide range of frictional velocities, atmospheric pressures, and insolations and it seems clear that at least some subset of observed Martian channels may have formed as ice-choked rivers. Typical equilibrium thicknesses of such ice covers are ～ 10 to 30 m; typical surface temperatures are 210 to 235°K. Ice-covered channels or lakes on Mars today may be of substantial biological interest. Ice is a sufficiently poor conductor of heat that sunlight which penetrates it can cause melting to a depth of several meters or more. Because the obliquity of Mars can vary up to some 35°, the increased polar heating at such times seems able to cause subsurface melting of the ice caps to a depth which corresponds to the observed lamina thickness and may be responsible for the morphology of these polar features.     

Ozone and photochemistry of the Martian lower atmosphere

The calculation of number densities of CO₂, H₂O and N₂ photolysis products was carried out for the Martian atmosphere at heights up to 60 km. The ozone distributed in the atmosphere as a layer of 10 km width with [O₃] max = 2.5 × 10⁹ cm³ at height of 35 km which agree well with the results of u.v. observations on the evening terminator from the Mars-5 satellite. The calculated densities of O₂, CO and H₂O are also in good agreement with the measured data. The eddy diffusion coefficient is equal to 3 × 10⁶ in the troposphere (h ? 30 km) and 10⁸ cm² s^?1 above 40 km. The dependence of the total ozone content on water vapour amount in the atmosphere is considered; the hypothesis about the influence of water ice aerosol on the ozone formation is proposed to explain the high concentrations of ozone in the morning.     

The Martian Hadley circulation: Comparison of “viscous” model predictions to observations

The predictions of an analytical steady thermally forced viscous model for the zonally averaged global circulation of the Martian atmosphere are compared to observations of atmospheric temperatures and eolian feature directions. The temperature of the winter polar atmosphere is a sensitive indicator of the value of the mean eddy diffusivity v of the atmosphere. For global dust storm season, the observed large warming of the atmosphere over the winter (north) pole during the 1977b storm as well as the distribution and azimuths of Type I(b) dust streaks can be well reproduced if v = 10⁷−10⁸cm²sec⁻¹. Observed northeasterly surface winds at high northern latitudes could be produced by plausible fluxes of CO₂ from the northern polar cap. The thermal structure at southern latitudes during this storm is satisfactorily produced, but a major discrepancy exists between observations and predictions of the temperature structure at middle northern latitudes. By comparing these results with those from previous inviscid models of the zonal mean circulation on Mars, we suggest v > 10⁷cm²sec⁻¹ at heights above 30 km and v ⪡ 10⁷cm²sec⁻¹ at lower altitudes may yield a meridional circulation which produces the dynamical warming necessary to account for the observed thermal structure at 0.6 mbar at all latitudes. For late southern summer when the dust content of the atmosphere has decreased to levels characteristic of much of the Martian year, the lack of dynamical warming of the winter pole implies v ≤ 10⁶cm²sec⁻¹. In addition, the predicted surface wind azimuths at this season agree well with the observed azimuths of Type I(d) dust streaks, which are observed to form at this season. The observed latitudinal concentration of the streaks is not explained by the model and may require additional processes which have not been included.     

Can rapid loss and high variability of Martian methane be explained by surface H2O2?

It has been reported by several groups that methane in the Martian atmosphere is both spatially and temporally variable. Gough et al. (2010) suggested that temperature dependent, reversible physical adsorption of methane onto Martian soils could explain this variability. However, it is also useful to consider if there might be chemical destruction of methane (and compensating sources) operating on seasonal time scales. The lifetime of Martian methane due to known chemical loss processes is long (on the order of hundreds of years). However, observations constrain the lifetime to be 4 years or less, and general circulation models suggest methane destruction must occur even faster (<1 year) to cause the reported variability and rapid disappearance. The Martian surface is known to be highly oxidizing based on the Viking Labeled Release experiments in which organic compounds were quickly oxidized by samples of the regolith. Here we test if simulated Martian soil is also oxidizing towards methane to determine if this is a relevant loss pathway for Martian methane. We find that although two of the analog surfaces studied, TiO₂·H₂O₂ and JSC-Mars-1 with H₂O₂, were able to oxidize the complex organic compounds (sugars and amino acids) used in the Viking Labeled Release experiments, these analogs were unable to oxidize methane to carbon dioxide within a 72 h experiment. Sodium and magnesium perchlorate, salts that were recently discovered at the Phoenix landing site and are potential strong oxidants, were not observed to directly oxidize either the organic solution or methane. The upper limit reaction coefficient, α, was found to be <4×10^?17 for methane loss on TiO₂·H₂O₂ and <2×10^?17 for methane loss on JSC-Mars-1 with H₂O₂. Unless the depth of soil on Mars that contains H₂O₂ is very deep (thicker than 500 m), the lifetime of methane with respect to heterogeneous oxidation by H₂O₂ is probably greater than 4 years. Therefore, reaction of methane with H₂O₂ on Martian soils does not appear to be a significant methane sink, and would not destroy methane rapidly enough to cause the reported atmospheric methane variability.     

Multiple emission angle surface-atmosphere separations of thermal emission spectrometer data

A method for separating the spectral signatures of the Martian surface and atmosphere was developed and is applied to multiple emission angle data returned from the MGS TES instrument. This method includes correlated-k and index gas removal algorithms that may be applied to all nadir-pointing TES data. Initial results have provided new and refined measurements of the spectral shapes of atmospheric dust and the Martian surface. Surface temperatures and atmospheric dust opacities are also retrieved with improved accuracy over single observation temperature and opacity retrievals. Low-albedo surfaces display absorptions consistent in both shape and depth with previous studies. These surfaces may be closely modeled using a combination of previously derived basalt, andesitic, and high-albedo surface spectral shapes. Short wavelengths display no significant absorptions, indicating both the coarse particulate nature of the surface and the lack of significant amounts of carbonate. Moderate- and high-albedo surfaces have spectral shapes distinctive of fine particulate silicate materials. No single material can match the entire high-albedo surface spectrum, though there are clear indications of a material that closely matches intermediate to calcic plagioclase and an emission peak at ∼1620 cm⁻¹ due to bound water. The lack of residual restrahlen silicate absorptions indicates that minerals such as olivine or pyroxene are not present in high-albedo surfaces at significant (but unknown) abundances. High-albedo surface results presented here are in agreement with and complementary to shorter wavelength observations. The Martian dust is composed of both primary and secondary minerals. Either chemical weathering has not completely altered its source material or the soil is a mixture of altered and unaltered sources. Further laboratory studies are needed to better establish detection limits and behavior of mineral mixtures of fine particulates in the thermal infrared portion of the spectrum.     

Vertical distribution of water vapor and mars model lower and middle atmosphere

Observations and model calculations of water vapor diffusion suggest that about half the amount of water vapor is distributed with constant mixing ratio in the Martian atmosphere, the other half is the excess water vapor in the lower troposphere. During 24 hr the total content of water vapor may vary by a factor of two. The eddy diffusion coefficient providing agreement between calculations and observations is K = (3–10) × 10⁶ cm² sec^?1 in the troposphere. An analytical expression is derived for condensate density in the stratosphere in terms of the temperature profile, the particle radius r, and K. The calculations agree with the Mars 5 measurements for r = 1.5 μm, condensate density 5 × 10^?12 g/cm³ in the layer maximum at 30 to 35 km, condensate column density 7 × 10^?6 cm^?2, K = (1?3) × 10⁶ cm² sec^?1, and the temperature profile T = 185 ? 0.05z ? 0.01z² at 20 to 40 km. Condensation conditions yield a temperature of 160°K at 60 km in the evening; the scale height for scattered radiation yields T = 110°k at 80 to 90 km. The Mars model atmosphere has been developed up to 125 km.     

Lightnings and nitric oxide on Venus

In an updating of energy characteristics of lightnings on Venus obtained from Venera-9 and -10 optical observations, the flash energy is given as 8 × 10⁸ J and the mean energy release of lightnings is 1 erg cm^?2 s which is 25 times as high as that on the Earth. Lightnings were observed in the cloud layer. The stroke rate in the near-surface atmosphere is less than 5 s^?1 over the entire planet if the light energy of the stroke exceeds 4 × 10⁵ J and less than 15 s^?1 for (1–4) × 10⁵ J.The average NO production due to lightnings equals 5 × 10⁸ cm^?2 s^?1, the atomic nitrogen production is equal to 7 × 10⁹ cm^?2s^?1,the N flux toward the nightside is 3.2 × 10⁹ cm^?2s^?1, the number densities [N] = 3 × 10⁷cm^?3 and [NO] = 1.8 × 10⁶cm^?3 at 135 km. Almost all NO molecules in the upper atmosphere vanish interacting with N and the resulting NO flux at 90-80 km equals 5 × 10⁵cm^?2s^?1, which is negligibly small as compared with lightning production. If the predissociation at 80–90 km is regarded as the single sink of NO, its mixing ratio, f_NO, is 4 × 10^?8, for the case of a surface sink f_NO = 0.8 × 10^?9 at 50 km. Excess amounts, $\text{f}{}_{\mathrm{<mtext>NO</mtext>}}\text{? 4 × 10}{}^{\mathrm{?8}}$, may exist in the thunderstorm region.     

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.     

The structure and microphysical properties of the Venus clouds: Venera 9, 10, and 11 data

Data processing and interpretation of the nephelometer measurements made in the Venus atmosphere aboard the Venera 9, 10 and 11 landers in the sunlit hemisphere near the equator are discussed. These results were used to obtain the aerosol distribution and its microphysical properties from 62 km to the surface. The main aerosol content is found in the altitude range between 62 km (where measurements began) and 48 km, the location of the cloud region. Three prominent layers labeled as I (between 62 and 57 km), II (between 57 and 51 km) and III (between 51 and 48 km), each with different particle characteristics are discovered within the clouds. The measured light-scattering patterns can be intrepreted as having been produced by particles with effective radii from 1 to 2 μm depending on height and indices of refractivity from 1.45 in layer I to 1.42 in layer III. These values do not contradict the idea that the droplets are made of sulfuric acid. In layers II and III the particle size distribution is at least bimodal rather than uni-modal. The index of refraction is found to decrease to 1.33 in the lower part of layer II, suggesting a predominant abundance of larger particles of different chemical origin, and chlorine compounds are assumed to be relevant to this effect. In the entire heightrange of the Venera 9–11 craft descents, the clouds are rather rarefied and are characterized by a mean volume scattering coefficient σ ～ 2 × 10^?5 cm^?1 that corresponds to the mean meteorological range of visibility of about 2 km. The average mass content of condensate is estimated to be equal to 4 × 10^?9 g/cm³, and the total optical depth of clouds to τ ～ 35. Near the bottom of layer III clouds are strongly variable. In the subcloud atmosphere a haze was observed between 48 and 32 km; that haze is mainly made of submicron particles, r_eff ～ 0.1μm. The atmosphere below that is totally transparent but separate (sometimes possibly disappearing) layers may be present up to a height of 8 km above the surface. A model of this region with a very low particle density (N ? 2–3 cm^?3) strongly refractive large particles (r_eff ? 2.5 μm; 1.7 < n < 2.0) provided satisfactory agreement. The optical depth of aerosol in the atmosphere below the subcloud haze does not exceed 2.5.     

Thin magnetic hydrogen atmospheres and the neutron star RX J1856.5–3754

RX J1856.5–3754 is one of the brightest nearby isolated neutron stars, and considerable observational resources have been devoted to it. However, current models are unable to satisfactorily explain the data. We show that our latest models of a thin, magnetic, partially ionized hydrogen atmosphere on top of a condensed surface can fit the entire spectrum, from X-rays to optical, of RX J1856.5–3754, within the uncertainties. In our simplest model, the best-fit parameters are an interstellar column density N _H≈1×10²⁰ cm^?2 and an emitting area with R ^∞≈17 km (assuming a distance to RX J1856.5–3754 of 140 pc), temperature T ^∞≈4.3×10⁵ K, gravitational redshift z _g ～0.22, atmospheric hydrogen column y _H≈1 g cm^?2, and magnetic field B≈(3–4)×10¹² G; the values for the temperature and magnetic field indicate an effective average over the surface.     

Physical properties of the particles composing the Martian dust storm of 1971–1972

Infrared spectra obtained from the Mariner 9 spacecraft during the 1971–1972 dust storm are used to derive information on the composition and particle size distribution of the dust and to study the time evolution of the storm. The dust is not composed of pure granite, basalt, basaltic glass, obsidian, quartz, andesite, or montmorillonite. The infrared spectra suggest that the dust is a mixture of materials, dominated by igneous silicates with >62;60% SiO₂, or weathering products such as clay minerals, but the dust could possibly have a significant component of lower SiO₂ materials such as basalt. Substantial quantities of carbonates, nitrates, or carbon suboxide are excluded from the mixture. All infrared, visible, and ultraviolet data on the Martian surface composition seem consistent with a mixture of basalt and clay minerals or high SiO₂ igneous rocks, with a surface patina of oxides of iron. For all candidate compositions, the data are best matched with a size distribution that approximates a differential power law function of slope ?4. This size distribution is quite similar to terrestial size distributions in regions remote from sources of dust. The relative abundance of particles between 1- and 10-μm radius did not change during the Mariner 9 mission; thus suspended particles did not experience Stokes-Cunningham fallout but instead were supported by turbulence with an eddy diffusion coefficient, $\text{K}{}_{\mathrm{<mtext>e</mtext>}}\text{? 7 × 10}{}^6\text{cm}{}^2\text{sec}{}^{\mathrm{?1}}$. The aerosol optical depth, standardized to 0.3-μm wavelength, varied from about 1.5 early in the mission to about 0.2 at Orbit 200.     

A new hematite formation mechanism for Mars

Abstract— The origin of hematite detected in Martian surface materials is commonly attributed to weathering processes or aqueous precipitation. Here, we present a new hematite formation mechanism that requires neither water nor weathering. Glass‐rich basalts with Martian meteorite‐like chemistry (high FeO, low Al₂O₃) oxidized at high (700 and 900 °C) temperatures in air and CO₂, respectively, form thin (<1 μm) hematite coatings on their outermost surfaces. Hematite is manifested macroscopically by development of magnetism and a gray, metallic sheen on the glass surface and microscopically by Fe enrichment at the glass surface observed in element maps. Visible and near‐infrared, thermal infrared, and Raman spectroscopy confirm that the Fe enrichment at the oxidized glass surfaces corresponds to hematite mineralization. Hematite formation on basaltic glass is enabled by a mechanism that induces migration of Fe²⁺ to the surface of an oxidizing glass and subsequent oxidation to form hematite. A natural example of the hematite formation mechanism is provided by a Hawaiian basalt hosting a gray, metallic sheen that corresponds to a thin hematite coating. Hematite coating development on the Hawaiian basalt demonstrates that Martian meteorite‐like FeO contents are not required for hematite coating formation on basalt glass and that such coatings form during initial extrusion of the glassy basalt flows. If gray hematite originating as coatings on glassy basalt flows is an important source of Martian hematite, which is feasible given the predominance of igneous features on Mars, then the requirement of water as an agent of hematite formation is eliminated.     

Thermal structure of the Martian atmosphere during the dissipation of the dust storm of 1971

The secular variation of the thermal structure of the Martian atmosphere during the dissipation phase of the 1971 dust storm is examined, using temperatures obtained by the infrared spectroscopy investigation on Mariner 9. For the latitude range ?20° to ?30°, the mean temperature at the 2mbar level is found to decrease from approximately 220 K in mid-December 1971 to about 190 K by June 1972 while for the 0.3mbar level a decrease from 203 K to 160 K is observed. Over the same period, the amplitude of the diurnal temperature wave also decreased. Assuming a simplified radiative heating model, the dust optical depth is found to decrease approximately exponentially with an e-folding time of about 60 days at both the 0.3 and 2mbar levels. Stokes-Cunningham settling alone cannot account for this behavior. Sedimentation models which include both gravitational settling and vertical mixing are developed in an effort to explain the time evolution of the dust. Within the framework of a model which assumes an effective vertical diffusivity K independent of height, a mean dust particle diameter of ～2 μm is inferred. To provide the necessary vertical mixing, K ? 10⁷ cm²sec^?1 is required in the lower atmosphere.     

Far-infrared spectrophotometry of Saturn and its rings

The spectrum of Saturn was measured from 80 to 350 cm^?1 (29 to 125 μm) with ≈6-cm^?1 resolution using a Michelson interferometer aboard NASA's Kuiper Airborne Observatory. These observations are of the full disk, with little contribution from the rings. For frequencies below 300 cm^?1, Saturn's brightness temperature rises slowly, reaching ≈111°K at 100 cm^?1. The effective temperature is 96.8 ± 2.5°K, implying that Saturn emits 3.0 ± 0.5 times as much energy as it receives from the Sun. The rotation-inversion manifolds of NH₃ that are prominent in the far-infrared spectrum of Jupiter are not observed on Saturn. Our models predict the strengths to be only ≈2 to 5°K in brightness temperature because most of the NH₃ is frozen out; this is comparable to the noise in our data. By combining our data with those of an earlier investigation when the Saturnicentric latitude of the Sun was B′ = 21.2°, we obtain the spectrum of the rings. The high-frequency end of the ring spectrum (ν > 230 cm^?1) has nearly constant brightness temperature of 85°K. At lower frequencies, the brightness temperature decreases roughly as predicted by a simple absorption model with an optical depth proportional to ν^1.5. This behavior could be due to mu-structure on the surface of the ring particles with a scale size of 10 to 100 μm and/or to impurities in their composition.     

A study of the 3ν3CH4 region in a high-resolution spectrum of Jupiter recorded by Fourier transform spectroscopy

A spectrum of Jupiter between 6000 and 12 000 cm^? at high resolution (0.05 cm^?) was recorded with a Michelson interferometer at Palomar Mountain in October 1974. An analysis of the R branch of the 3ν₃CH₄ band with the reflecting-layer model, taking into account the H₂ absorption which occurs in the same spectral range, leads to a Lorentzian half-width of 0.09 ± 0.02 cm^?1, a rotational temperature of 175 ± 10° K, and a CH₄ abundance of order 52m atm. Five lines of the ¹³CH₄3ν₃ band have been identified; a comparison with new laboratory spectra indicates that the ¹³CH₄/¹²CH₄ ratio in the Jupiter atmosphere is close to the terrestrial ratio.     

The upper Jovian atmosphere aerosol content determined from a satellite eclipse observation

The Galilean satellite eclipse technique for measuring the aerosol distribution in the upper Jovian atmosphere is described and applied using 30 color observations of the 13 May 1972 eclipse of Ganymede obtained with the 5-m Hale telescope. This event probes the South Temperate Zone. The observed aerosol lies above the visible cloud tops, is very tenuous and varies with altitude, increasing rapidly with downward passage through the tropopause. The aerosol extinction coefficient, κ_a (λ1.05 μm), is ～1.1 × 10^?9 cm^?1 in the lower stratosphere and ～1.1 × 10^?8 cm^?1 at the tropopause. The 1σ uncertainty in these values does not exceed 50% The observations require some aerosol above the tropopause but do not clearly determine its structure. The present analysis emphasizes an extended haze distribution, but the alternate possibility is not excluded that the stratospheric aerosol resides in a thin layer. The aerosol extinction increases with decreasing wavelength and indicates the particle radius to be ?0.2 μm. Larger radii are impossible. These overall results confirm Axel's (1972) suggestion of a small quantity of dust above the Jovian cloud tops and the optical depths are consistent with those required to explain the low uv albedo.     

Statistical analysis of the observations of the MEX/ASPERA-3 NPI in the shadow

The analyser of space plasma and energetic atoms (ASPERA-3) neutral particle imager (NPI) on board Mars Express (MEX) is devoted to energetic neutral atom (ENA) detection within the Martian environment. These ENAs originate from the interaction between the energetic ions flowing inside the Martian environment and the exospheric neutral gas, thus providing crucial information about the dynamics of this interaction. NPI records the instantaneous angular distribution of the energy-integrated ENA signal. In order to identify recurrent ENA signals in the Martian environment, we have performed a statistical analysis of the NPI data. Count rates have been averaged using different methods in order to be able to discriminate signals coming from the planet, from a selected direction, or from specific planetographic regions at the planetary surface. Possible recurrent ENA signals (about 5×10⁶ (cm² sr s)^?1) are found coming from the terminator direction and above the atmosphere toward nightside when the spacecraft was inside the planetary shadow, mainly close to the shadow edge. Some significant signal was found from the anti-Mars directions in 2005. No statistically significant signal related to pick-up ions from the atmosphere or related to magnetic anomalies above the sensor intrinsic error (estimated as 3×10⁶ (cm² sr s)^?1) was observed. Our analysis shows that particular attention should be given to the use of NPI data when performing statistical studies; in fact, the sensor has some intrinsic limitations due to inadequate UV suppression, difficulties in sector inter-calibrations, and variations in the sector response versus time.     

Mars: Experimental study of albedo changes caused by dust fallout

An experimental study was undertaken to determine how the spectral and photometric properties of representative Martian areas are affected by fallout of atmospheric dust suspended during dust forms. A laboratory apparatus was used to simulate the uniform fallout and deposition of particles 1 to 5 μm in diameter. Spectral measurements from 0.4- to 1.2-μm wavelengths and photometric measurements at several wavelengths were made for a number of Mars-analog materials before and after deposition of 6 × 10^?5 to 1.5 × 10^?3 g/cm² of simulated fallout. These results indicate that the spectral and photometric properties of Martian regions can be affected significantly even by minute amounts of fallout. For instance, the reflectance at 0.56 μm of an average dark area will increase by 35% after deposition of only 9 × 10^?5 g/cm², and by 70% after deposition of 1.5 × 10^?4 g/cm². Thus the fallout from even one dust storm season (～2 × 10^?3 g/cm²) is sufficient to change significantly the spectral and photometric characteristics of the substrate material, if the fallout were ubiquitous over the surface and if no competing processes of dust removal from surface grains occured.     

AOST: Fourier spectrometer for studying mars and phobos

An AOST Fourier spectrometer of the Phobos-Soil project is intended for studying Mars and Phobos by means of measurements of IR radiation spectra of the Martian surface and atmosphere, the Phobos surface, and the spectrum of solar radiation passing through the Martian atmosphere on its limb. The main scientific problems to be solved with the spectrometer on Mars are measurements of methane content, search for minor constituents, and study of diurnal variations in the temperature and atmospheric aerosol. The spectrometer will also study the Martian and Phobos surface both remotely and after landing. The spectral range of the instrument is 2.5?C25 ??m, the best spectral resolution (without apodization) is 0.6 cm^?1, and the instantaneous field of view is 2.5°. The recording time of one spectrum is equal to 5 s in solar observations and 50 s in observations of Mars and Phobos. The instrument has self-thermal stabilization and two-axis pointing systems, as well as a built-in radiation source for flight calibration. The spectrometer mass is 4 kg, and power consumption is up to 13 W. Scientific problems, measurement modes, and, briefly, engineering implementation of the experiment are discussed in this work.