Thick and thin models of the evolution of carbon dioxide on Mars

We present results from a new simulation code that accounts for the evolution of the reservoirs of carbon dioxide on Mars, from its early years to the present. We establish a baseline model parameter set that produces results compatible with the present (i.e., Patm?6.5 mbar with permanent CO₂ ice cap) for a wide range of initial inventories. We find that the initial inventory of CO₂ broadly determines the evolutionary course of the reservoirs of CO₂. The reservoirs include the atmosphere, ice cap, adsorbed CO₂ in the regolith, and carbonate rocks. We track the evolution of the free inventory: the atmosphere, ice cap and regolith. Simulations begin at 4.53 Gyr before present with a rapid loss of free inventory to space in the early Noachian. Models that assume a relatively small initial inventory (?5 bar) have pronounced minima in the free inventory of CO₂ toward the end of the Noachian. Under baseline parameters, initial inventories below ∼4.5 bar result in a catastrophic loss of the free inventory to space. The current free inventory would be then determined by the balance between outgassing, sputtering losses and chemical weathering following the end of the late bombardment. We call these “thin” models. They generically predict small current free inventories in line with expectations of a small present CO₂ ice cap. For “thick” models, with initial inventories ?5 bar, a surplus of 300-700 mbar of free CO₂ remains during the late-Noachian. The histories of free inventory in time for thick models tend to converge within the last 3.5 Gyr toward a present with an ice cap plus atmospheric inventory of about 100 mbar. For thick models, the convergence is largely due to the effects of chemical weathering, which draws down higher free inventories more rapidly than the low. Thus, thick models have ?450 mbar carbonate reservoirs, while thin models have ?200 mbar. Though both thick and thin scenarios can reproduce the current atmospheric pressure, the thick models imply a relatively large current CO₂ ice cap and thin models, little or none. While the sublimation of a massive cap at a high obliquity would create a climate swing of greenhouse warming for thick models, under the thin model, mean temperatures and pressures would be essentially unaffected by increases in obliquity.     

The role of seasonal reservoirs in the Mars water cycle: II. Coupled models of the regolith,the polar caps,and atmospheric transport

The behavior of water vapor in the Mars atmosphere requires that there be a seasonally accessible nonatmospheric reservoir of water. Coupled models have been constructed which include exchange of water with the regolith and with the polar caps, and transport through the atmosphere due to its circulation. Comparison of the model results with the vapor observations and with other data regarding the physical nature of the surface allows constraints to be placed on the relative importance of each process. The models are capable of satisfactorily explaining the gross features of the observed behavior using plausible values for the regolith and atmosphere mixing terms. In the region between the polar caps, the regolith contributes as much water to the seasonal cycle of vapor as does transport in from the more-poleward regions, to within a factor of 2. Globally, 10–40% of the seasonal cycle of vapor results from exchange of water with the regolith, about 40% results from the behavior of the residual caps, and the remainder is due to exchange of water with the seasonal caps. It is difficult to determine the relative importance of the processes more precisely than this because both regolith and polar cap exchange of water act to first order in the same direction, producing the largest vapor abundance during the local summer. The system is ultimately regulated on the seasonal time scale by the polar caps, as the time to reach equilibrium between the atmosphere and regolith or between the polar atmosphere and the global atmosphere is much longer than the time for the polar caps to equilibrate with the local atmosphere. This same behavior will hold for longer time scales, with the polar caps being in equilibrium with the insolation as it changes on the obliquity time scale, and the atmosphere and regolith following along.     

The astronomical theory of climatic change on Mars

We examine the response of Martian climate to changes in solar energy deposition caused by variations of the Martian orbit and obliquity. We systematically investigate the seasonal cycles of carbon dioxide, water, and dust to provide a complete picture of the climate for various orbital configurations. We find that at low obliquity (15°) the atmospheric pressure will fall below 1 mbar; dust storms will cease; thick permanent CO₂ caps will form; the regolith will release CO₂; and H₂O polar ice sheets will develop as the permafrost boundaries move poleward. At high obliquity (35°) the annual average polar temperature will increase by about 10°K, slightly desorbing the polar regolith and causing the atmospheric pressure to increase by not more than 10 to 20 mbar. Summer polar ground temperatures as high as 273°K will occur. Water ice caps will be unstable and may disappear as the equilibrium permafrost boundary moves equatorward. However, at high eccentricity, polar ice sheets will be favored at one pole over the other. At high obliquity dust storms may occur during summers in both hemispheres, independent of the eccentricity cycle. Eccentricity and longitude of perihelion are most significant at modest obliquity (25°). At high eccentricity and when the longitude of perihelion is close to the location of solstice hemispherical asymmetry in dust-storm generation and in polar ice extent and albedo will occur.The systematic examination of the relation of climate and planetary orbit provides a new theory for the formation of the polar laminae. The terraced structure of the polar laminae originates when eccentricity and/or obliquity variations begin to drive water ice off the dusty permanent H₂O polar caps. Then a thin (meters) layer of consolidated dust forms on top of a dirty, slightly thicker (tens of meters) ice sheet and the composite is preserved as a layer of laminae composed predominately of water ice. Because of insolation variation on slopes, a series of poleward- and equatorward-facing scarps are formed where the edges of the laminae are exposed. Independently of orbital variations, these scarps propagate poleward both by erosion of the equatorward slopes and by deposition on the poleward slopes. Scarp propagation resurfaces and recycles the laminae forming the distinctive spiral bands of terraces observed and provides a supply of water to form new permanent ice caps. The polar laminae boundary marks the furthest eqautorward extension of the permanent H₂O caps as the orbit varies. The polar debris boundary marks the furthest equatorward extension of the annual CO₂ caps as the orbit varies.The Martian regolith is now a significant geochemical sink for carbon dioxide. CO₂ has been irreversibly removed from the atmosphere by carbonate formation. CO₂ has also benn removed by regolith adsorption. Polar temperature increases caused by orbital variations are not great enough     

Loss of water from Mars:: Implications for the oxidation of the soil

The evolution of the martian atmosphere with regard to its H₂O inventory is influenced by thermal loss processes of H, H₂, nonthermal atmospheric loss processes of H⁺, H₂⁺, O, O⁺, CO₂, and O₂⁺ into space, as well as by chemical weathering of the surface soil. The evolution of thermal and nonthermal escape processes depend on the history of the intensity of the solar XUV radiation and the solar wind density. Thus, we use actual data from the observation of solar proxies with different ages from the Sun in Time program for reconstructing the Sun's radiation and particle environment from the present to 3.5 Gyr ago. The correlation between mass loss and X-ray surface flux of solar proxies follows a power law relationship, which indicates a solar wind density up to 1000 times higher at the beginning of the Sun's main sequence lifetime. For the study of various atmospheric escape processes we used a gas dynamic test particle model for the estimation of the pick up ion loss rates and considered pick up ion sputtering, as well as dissociative recombination. The loss of H₂O from Mars over the last 3.5 Gyr was estimated to be equivalent to a global martian H₂O ocean with a depth of about 12 m, which is smaller than the values reported by previous studies. If ion momentum transport, a process studied in detail by Mars Express is significant on Mars, the water loss may be enhanced by a factor of about 2. In our investigation we found that the sum of thermal and nonthermal atmospheric loss rates of H and all nonthermal escape processes of O to space are not compatible with a ratio of 2:1, and is currently close to about 20:1. Escape to space cannot therefore be the only sink for oxygen on Mars. Our results suggest that the missing oxygen (needed for the validation of the 2:1 ratio between H and O) can be explained by the incorporation into the martian surface by chemical weathering processes since the onset of intense oxidation about 2 Gyr ago. Based on the evolution of the atmosphere-surface-interaction on Mars, an overall global surface sink of about 2×10⁴² oxygen particles in the regolith can be expected. Because of the intense oxidation of inorganic matter, this process may have led to the formation of considerable amounts of sulfates and ferric oxides on Mars. To model this effect we consider several factors: (1) the amount of incorporated oxygen, (2) the inorganic composition of the martian soil and (3) meteoritic gardening. We show that the oxygen incorporation has also implications for the oxidant extinction depth, which is an important parameter to determine required sampling depths on Mars aimed at finding putative organic material. We found that the oxidant extinction depth is expected to lie in a range between 2 and 5 m for global mean values.     

Some problems related to the origin of methane on Mars

The following problems related to the origin of methane on Mars have been considered. (1) Laboratory simulations of the impact phenomena confirm effective heterogeneous chemistry between the products of the fireball. This chemistry lowers the fireball freezing temperature from 2000 to 750 K for methane and to 1100 K for CO/CO₂. Production of methane on Mars by cometary impacts is 0.8% of the total production. A probability that the observed methane on Mars came from impact of a single comet is 0.0011. (2) The PFS observations of variations of methane on Mars require a very effective heterogeneous loss of methane. Heterogeneous effect of dust is half that of the surface rocks. Thermochemical equilibrium requires production, not loss, of methane. Existing kinetic data show a very low efficiency of heterogeneous reactions of methane. Highly reactive superoxide ions generated by the solar UV photons on the martian rocks cannot remove methane. The required efficiency of heterogeneous loss of methane on Mars is higher than that on Earth by a factor of ?1000, although the expected efficiency on Earth is stronger than that on Mars because of the liquid ocean and the abundant oxygen. All these inconsistencies may be removed if variations of the rock reflectivity contribute to the PFS observations of methane on Mars. The PFS data on H₂CO, HCl, HF, and HBr also raise doubts. (3) Although geologic sources of methane are possible, the lack of current volcanism, hydrothermal activity, hot spots, and very low seepage of gases from the interior are not favorable for geologic methane. Any proposed geological source of methane on Mars should address these problems. Some weak points in the suggested geologic sources are discussed. (4) Measurements of ¹³C/¹²C and D/H in methane would be difficult because of the low methane abundance. These ratios are mostly sensitive to a temperature of methane formation and cannot distinguish between biogenic and low-temperature geologic sources. Their analysis requires the carbon isotope ratio in CO₂ on Mars, which is known with the insufficient accuracy, and D/H in water, which is different in the atmosphere, polar caps, regolith and interior. Therefore, the stable isotope ratios may not give a unique answer on the origin of methane. (5) Ethane and propane react with OH much faster than methane. If their production relative to methane is similar to that on Earth, then their expected abundances on Mars are of a few parts per trillion. (6) Loss of SO₂ in the reaction with peroxide on ice is smaller than its gas-phase loss by an order of magnitude. The overall results strengthen the biogenic origin of martian methane and its low variability.     

Martian volatiles: Their degassing history and geochemical fate

Observations of Mars and cosmochemical considerations imply that the total inventory of degassed volatiles on Mars is 10² to 10³ times that present in Mars' atmosphere and polar caps. The degassed volatiles have been physically and chemically incorporated into a layer of unconsolidated surface rubble (a “megaregolith”) up to 2km thick. Tentative lines of evidence suggest a high concentration (～5g/cm²) of ⁴⁰ Ar in the atmosphere of Mars. If correct, this would be consistent with a degassing model for Mars in which the Martian “surface” volatile inventory is presumed identical to that of Earth but scaled to Mars' smaller mass and surface area. The implied inventory would be: (⁴⁰Ar) = 4g/cm², (H₂O) = 1 × 10⁵g/cm², (CO₂) = 7 × 10³g/cm², (N₂) = 3 × 10²g/cm², (Cl) = 2 × 10³g/cm², and (S) = 2 × 10²g/cm². Such a model is useful for testing, but differences in composition and planetary energy history may be anticipated between Mars and Earth on theoretical grounds. Also, the model demands huge regolith sinks for the volatiles listed.If the regolith were in physical equilibrium with the atmosphere, as much as 2 × 10⁴g/cm² of H₂O could be stored in it as hard-frozen permafrost, or 5 × 10⁴g/cm² if equilibrium with the atmosphere were inhibited. Spectral measurements of Martian regolith material and laboratory measurement of weathering kinetics on simulated regolith material suggest large amounts of hydrated iron oxides and clay minerals exist in the regolith; the amount of chemically bound H₂O could be from 1 × 10⁴ to 4 × 10⁴g/cm². In an Earth-analogous model, a 2 km mixed regolith must contain the following concentrations of other volatile-containing compounds by weight: carbonates = 1.5%, nitrates = 0·3%, chlorides = 0.6%, and sulfates = 0.1%. Such concentrations would be undetectable by current Earth-based spectral reflectance measurements, and (except the nitrates) formation of the “required” amounts of these compounds could result from interaction of adsorbed H₂O and ice with primary silicates expected on Mars. Most of the CO₂ could be physically adsorbed on the regolith.Thus, maximum amounts of H₂O and other volatiles which could be stored in the Mars regolith are marginally compatible with those required by an Earth-analogous model, although a lower atmospheric ⁴⁰Ar concentration and regolith volatile inventory would be easier to reconcile with observational constraints. Differences in the ratios of H₂O and other volatiles to ⁴⁰Ar between surface volatiles on the real Mars and on an Earth-analogous Mars could result from and reflect differences in bulk composition and time history of degassing between Mars and Earth. Models relating Viking-observable parameters, e.g., (⁴⁰Ar) and (³⁶Ar), to the time history and overall intensity of Mars degassing are given.     

A 1 Gyr climate model for Mars: new orbital statistics and the importance of seasonally resolved polar processes

New results from a 1 Gyr integration of the martian orbit are presented along with a seasonally resolved energy balance climate model employed to illuminate the gross characteristics of the long-term atmospheric pressure evolution. We present a new analysis of the statistical variation of the martian obliquity and precession prior to and subsequent to the formation of the Tharsis uplift, and explore the long term effects on the martian climate. We find that seasonal polar cycles have a critical influence on the ability for the regolith to release CO₂ at high obliquities, and find that the atmospheric CO₂ actually decreases at high obliquities due to the cooling effect of polar deposits at latitudes where seasonal caps form. At low obliquity, the formation of massive, permanent polar caps depends critically on the values of the frost albedo, A_frost, and frost emissivity, ?_frost. Using our model with values of A_frost=0.67 and ?_frost=0.55, matched to the NASA Ames General Circulation Model (GCM) results (Haberle et al., 1993, J. Geophys. Res. 98, 3093-3123, and Haberle et al., 2003, Icarus 161, 66-89), we find that permanent caps only form at low obliquities (<13°), suggesting that any permanent deposits on the surface of Mars today may be residuals left over from a period of very low obliquity, or are the result of mechanisms not represented by this model. Thus, contrary to expectations, the martian atmospheric pressure is remarkable static over time, and decreases both at high and low obliquity. Also, from our one billion year orbital model, we present new results on the fraction of time Mars is expected to experience periods of low obliquity and high obliquity.     

Regolith-atmosphere exchange of water and carbon dioxide on Mars: Effects on atmospheric history and climate change

Exchange of CO₂ and H₂O between the Mars regolith and the atmosphere-cap system plays an important role in governing the evolution of the martian atmosphere and the martian climate. Most of the exchangeable CO₂ (perhaps one or two orders of magnitude more than the atmospheric inventory) is currently adsorbed on the deep regolith, and can be “cryopumped” to a large quasipermanent CO₂ cap (not now present) during lowest Mars obliquity (θ). During the obliquity driven regolith-cap CO₂ exchange cycle, the atmospheric pressure varies harmonically between ~0.1 mb (lowest Θ) and ? 20 mb (highest Θ). The regolith buffer plays only a small or negligible role in the seasonal CO₂ pressure variations caused by atmosphere-cap exchange because adsorption greatly inhibits diffusion of the seasonal “pressure wave” into the regolith. In contrast, thermally driven H₂O seasonal exchange between the atmosphere and regolith appears to be in large part responsible for observed seasonal variations in the small atmospheric H₂O inventory. Long term exchange of H₂O may be dominated by transfer between the polar caps and ice in the regolith. Available and potential tests of regolith-atmospheric-cap volatile exchange models using ground-based and spacecraft-based techniques are discussed.     

Seasonal buffering of atmospheric pressure on Mars

An isothermal reservoir of carbon dioxide in gaseous contact with the Martian atmosphere would reduce the amplitude and advance the phase of global atmospheric pressure fluctuations caused by seasonal growth and decline of polar CO₂ frost caps. Adsorbed carbon dioxide in the upper ～10 m of Martian regolith is sufficient to buffer the present atmosphere on a seasonal basis. Available observations and related polar cap models do not confirm or refute the operation of such a mechanism. Implications for the amplitude and phase of seasonal pressure fluctuations are subject to direct test by the upcoming Viking mission to Mars.     

Depletion of sulfur on the surface of asteroids and the moon

Abstract— Data from the X‐ray and γ‐ray spectrometers onboard the Near Earth Asteroid Rendezvous (NEAR) spacecraft were used to constrain the chemical and mineralogical composition of asteroid 433 Eros (McCoy et al. 2001). The bulk composition appears to be consistent with that of L to H chondrites (Nittler et al. 2001). However, there appeared to be a marked depletion relative to ordinary chondritic composition in the S/Si ratio (0.014 ± 0.017). We investigate space weathering mechanisms to determine the extent to which sulfur can be preferentially lost from the surface regolith. The two processes considered are impact vaporization by the interplanetary meteoroid population and ion sputtering by the solar wind. Using impact data for Al projectiles onto enstatite, we find that the vaporization rate for troilite (FeS) is nine times as fast as that for the bulk of the regolith. If 20% of the iron is in the form of troilite, then the net vaporization rate, normalized to bulk composition, is 2.8 times faster for sulfur than for iron. Sputtering is equally efficient at removing sulfur as impact vaporization.     

Radiative habitable zones in martian polar environments

The biologically damaging solar ultraviolet (UV) radiation (quantified by the DNA-weighted dose) reaches the martian surface in extremely high levels. Searching for potentially habitable UV-protected environments on Mars, we considered the polar ice caps that consist of a seasonally varying CO2 ice cover and a permanent H2O ice layer. It was found that, though the CO2 ice is insufficient by itself to screen the UV radiation, at approximately 1 m depth within the perennial H2O ice the DNA-weighted dose is reduced to terrestrial levels. This depth depends strongly on the optical properties of the H2O ice layers (for instance snow-like layers). The Earth-like DNA-weighted dose and Photosynthetically Active Radiation (PAR) requirements were used to define the upper and lower limits of the northern and southern polar Radiative Habitable Zone (RHZ) for which a temporal and spatial mapping was performed. Based on these studies we conclude that photosynthetic life might be possible within the ice layers of the polar regions. The thickness varies along each martian polar spring and summer between approximately 1.5 and 2.4 m for H2O ice-like layers, and a few centimeters for snow-like covers. These martian Earth-like radiative habitable environments may be primary targets for future martian astrobiological missions. Special attention should be paid to planetary protection, since the polar RHZ may also be subject to terrestrial contamination by probes.     

Measurements of the north polar cap of Mars and the Earth's northern hemisphere ice and snow cover

The boundaries of the polar caps of Mars have been measured on more than 3000 photographs since 1905 from the plate collection at the Lowell Observatory. For the Earth, the polar caps have been accurately mapped only since the mid 1960's when satellites were first available to synoptically view the polar regions. The polar caps of both planets wax and wane in response to changes in the seasons, and interannual differences in polar cap behavior on Mars as well as Earth are intimately linked to global energy balance. Data on the year to year variations in the extent of the north polar caps of Mars and Earth have been assembled and compared, although only 6 years of concurrent data were available for comparison.     

Rummaging through Earth's Attic for Remains of Ancient Life

We explore the likelihood that early remains of Earth, Mars, and Venus have been preserved on the Moon in high enough concentrations to motivate a search mission. During the Late Heavy Bombardment, the inner planets experienced frequent large impacts. Material ejected by these impacts near the escape velocity would have had the potential to land and be preserved on the surface of the Moon. Such ejecta could yield information on the geochemical and biological state of early Earth, Mars, and Venus. To determine whether the Moon has preserved enough ejecta to justify a search mission, we calculate the amount of terran material incident on the Moon over its history by considering the distribution of ejecta launched from the Earth by large impacts. In addition, we make analogous estimates for Mars and Venus. We find, for a well-mixed regolith, that the median surface abundance of terran material is roughly 7 ppm, corresponding to a mass of approximately 20,000 kg of terran material over a 10×10-square-km area. Over the same area, the amount of material transferred from Venus is 1-30 kg and material from Mars as much as 180 kg. Given that the amount of terran material is substantial, we estimate the fraction of this material surviving impact with intact geochemical and biological tracers.     

A photochemical model of the martian atmosphere

The factors governing the amounts of CO, O2, and O3 in the martian atmosphere are investigated using a minimally constrained, one-dimensional photochemical model. We find that the incorporation of temperature-dependent CO2 absorption cross sections leads to an enhancement in the water photolysis rate, increasing the abundance of OH radicals to the point where the model CO abundance is smaller than observed. Good agreement between models and observations of CO, O2, O3, and the escape flux of atomic hydrogen can be achieved, using only gas-phase chemistry, by varying the recommended rate constants for the reactions CO + OH and OH + HO2 within their specified uncertainties. Similar revisions have been suggested to resolve discrepancies between models and observations of the terrestrial mesosphere. The oxygen escape flux plays a key role in the oxygen budget on Mars; as inferred from the observed atomic hydrogen escape, it is much larger than recent calculations of the exospheric escape rate for oxygen. Weathering of the surface may account for the imbalance. Quantification of the escape rates of oxygen and hydrogen from Mars is a worthwhile objective for an upcoming martian upper atmospheric mission. We also consider the possibility that HOx radicals may be catalytically destroyed on dust grains suspended in the atmosphere. Good agreement with the observed CO mixing ratio can be achieved via this mechanism, but the resulting ozone column is much higher than the observed quantity. We feel that there is no need at this time to invoke heterogeneous processes to reconcile models and observations.     

Comparison of Earth and Mars as differentiated planets

Histories of the terrestrial planets are traceable to combinations of to five large-scale postaccretion processes: planetary differentiation, crustal differentiation, outgassing, plate tectonics, and recycling. All have operated on Earth to make a planet that was early differentiated into core, mantle, and crust and at very nearly the same time outgassed to form a differentiated crust, atmosphere and oceans. This gave rise to plate tectonics, recycling and thus two-way communication of the surface crust-atmosphere-ocean system with lower crust and upper mantle. Recycling of the Martian surface is probably restricted to limited chemical weathering of thin alteration surfaces of primary minerals because of the extreme slowness of diffusion controlled alteration where surfaces are not stripped by solution. There is evidence for neither subsidence of sedimentary basins nor subduction zones; thus internal recycling and two-way surface-interior communication is improbable. All sedimentary particles produced by mechanical erosion on Mars through its history are still at the surface or shallowly buried by later sediment. Any atmospheric components reacted with weathering crust are removed from the atmosphere. These and exospheric escape processes must have early reduced an original denser atmosphere to its present pressure after an early episode of planetary differentiation coupled to crustal differentiation and out-gassing. The early history of Mars may have been something like that of Earth until weathering and gas escape drew down its atmosphere.     

Martian Seasonal CO2 Ice in Polygonal Troughs in Southern Polar Region: Role of the Distribution of Subsurface H2O Ice

The Mars Orbiter Camera onboard the Mars Global Surveyor has obtained several images of polygonal features in the southern polar region. In images taken during the end of the southern spring, when the surrounding surface is free of the seasonal frost, CO₂ ice still appears to be present within the polygonal troughs. In Earth's polar regions, polygons such as these are indicative of water ice in the ground below. We analyzed the seasonal evolution of the thermal state and the CO₂ content of these features. Our 2-D model includes condensation and sublimation of the CO₂ ice, a self consistent treatment of the variations of the thermal properties of the regolith, and the seasonal variations of the local atmospheric pressure which we take from the results of a general circulation model. We find that the residence time of seasonal CO₂ ice in troughs depends not only on atmospheric opacity and albedo of the CO₂ ice, but also and most significantly on the distribution of water ice in the regolith. Optical properties of the atmosphere and surface CO₂ ice can be independently obtained from observations. To date this is not true about the distribution of water ice below the surface. Our analysis quantifies the dependence of the seasonal cycle of the CO₂ ice within the troughs on the assumed distribution of the water ice below the surface. We show that presence of water ice in the ground at a depth smaller than the depth of the troughs reduces winter condensation rate of CO₂ ice. This is due to higher heat flux conducted from the water ice rich regolith toward the facets of the troughs.     

Low pressure and desiccation effects on methanogens: Implications for life on Mars

Conditions on the surface of Mars would appear to be too hostile for life as we know it. But the subsurface is another matter. If liquid water is present, even intermittently, life forms present would at least be protected from the lethal radiation bombarding the surface. However, life would have to contend with variations in pressure and possibly extended periods of desiccation. The research reported here involves both active metabolism (methanogenesis) at 400 and 50 mbar of pressure, pressures that would be found in the near subsurface of Mars, and survival following desiccation at both 1 bar (a pressure that would be found in the Martian subsurface) and 6 mbar (the lowest pressure at the surface and very near subsurface). The three methanogens tested for active metabolism, Methanothermobacter wolfeii, Methanosarcina barkeri and Methanobacterium formicicum, all demonstrated methane production at both 400 and 50 mbar on JSC Mars-1, a Mars soil simulant. Methane production at 50 mbar was much reduced compared to that at 400 mbar, most likely due to the greater stress at the lower pressure. In desiccation survival experiments, M. barkeri had survived 330 days of desiccation at 1 bar, while M. wolfeii and M. formicicum survived 180 and 120 days, respectively. Methanococcus maripaludis did not survive desiccation at all at 1 bar. At 6 mbar, M. wolfeii, M. barkeri and M. formicicum survived 120 days of desiccation while M. maripaludis survived 60 days. These results along with results from previous research would seem to indicate that there is no reason that methanogens could not inhabit the subsurface of Mars.     

Computer Simulation of Sputtering of Lunar Regolith by Solar Wind Protons: Contribution to Change of Surface Composition and to Hydrogen Flux at the Lunar Poles

A computer simulation of the sputtering of lunar soil by solar wind protons was performed with the TRIM program. The rate of the sputtering-induced erosion of regolith particles was shown to be less than 0.2 Å per year. A preferential sputtering of Ca, Mg, and O was found along with a less intense sputtering of Fe, Si, and Ti. However, with no other selection mechanisms, surface concentrations of the atoms would differ from the volume ones by no more than 6 %. The enrichment of rims of regolith particles with iron occurs as a result of selective removal of lighter atoms from the lunar surface because of different energies of escape from the Moon's gravity. The energy distributions proved to be the same for all sorts of the sputtered atoms, except for implanted hydrogen; thus, a greater fraction of the atoms left on the lunar surface corresponds to heavier elements. According to simulation results, the concentration of reduced iron observed in the mature regolith could be attained during the time of regolith particle exposure to the present flux of solar wind (10⁵ years). Thus, sputtering can provide the concentration of Fe₀ observed in regolith. On periphery of a cloud of impact vapor the temperature is too low for an irreversible selective removal of evaporation products; thus, a meteoritic bombardment contributes to the formation of composition of the rims of regolith particles mainly through enrichment of the rims with elements from the bulk of the particles. The estimates of fluxes of backscattered solar wind protons and of sputtered protons, earlier implanted to the regolith, demonstrated that their contribution to the proton flux near the poles is only 10⁴ cm^–2 s^–1. This is by two orders of magnitude smaller than the proton flux from the Earth's magnetosphere which is, therefore, the main source of protons for permanently shaded polar craters of the Moon.     

A photohabitable zone in the martian snowpack? A laboratory and radiative-transfer study of dusty water-ice snow

Dusty water-ice snowpacks on Mars may provide a habitable zone for DNA based photosynthetic life. Previous work has over estimated the depths and thicknesses of such photohabitable zones by not considering the effect of red dust within the snowpack. For the summer solar solstice, at 80°N and a surface albedo of 0.45, there is a calculated photohabitable zone in the snowpack between depths of 5.5 and 7.5 cm. For an albedo of 0.62, there is a calculated photohabitable zone in the snowpack between depths of 8 and 11 cm. A coupled atmosphere-snow radiative-transfer model was set to model the Photosynthetic Active Radiation and DNA dose rates through water-ice snow at the north polar region of Mars. The optical properties of the polar caps were determined by creating a laboratory analogue to the Mars north polar deposits, and directly measuring light penetration and albedo. It is important for future exobiology missions to the polar regions of Mars to consider the implications of these findings, as drilling to depths of ∼11 cm should be sufficient to determine whether life exists within the martian snows, whether it is photosynthetic or otherwise, as at this depth the snow cover will provide a permanent protection from DNA damaging UV radiation.     

Numerical simulation of seasonal dynamics of water vapor in the Martian atmosphere

The seasonal evolution of the H₂O snow in the Martian polar caps and the dynamics of water vapor in the Martian atmosphere are studied. It is concluded that the variations of the H₂O mass in the polar caps of Mars are determined by the soil thermal regime in the polar regions of the planet. The atmosphere affects water condensation and evaporation in the polar caps mainly by transferring water between the polar caps. The stability of the system implies the presence of a source of water vapor that compensates for the removal of water from the atmosphere due to permanent vapor condensation in the polar residual caps. The evaporation of the water ice that is present in the surface soil layers in the polar regions of the planet is considered as such a source. The annual growth of the water-ice mass in the residual polar caps is estimated. The latitudinal pattern of the seasonal distribution of water vapor in the atmosphere is obtained for the stable regime.Translated from Astronomicheskii Vestnik, Vol. 38, No. 6, 2004, pp. 497–503.Original Russian Text Copyright © 2004 by Aleshin.