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1.
Recent observations suggest methane in the martian atmosphere is variable on short spatial and temporal scales. However, to explain the variability by loss reactions requires production rates much larger than expected. Here, we report results of laboratory studies of methane adsorption onto JSC-Mars-1, a martian soil simulant, and suggest that this process could explain the observations. Uptake coefficient (γ) values were measured as a function of temperature using a high-vacuum Knudsen cell able to simulate martian temperature and pressure conditions. Values of γ were measured from 115 to 135 K, and the data were extrapolated to higher temperatures with more relevance to Mars. Adsorptive uptake was found to increase at lower temperatures and larger methane partial pressures. Although only sub-monolayer methane surface coverage is likely to exist under martian conditions, a very large mineral surface area is available for adsorption as atmospheric methane can diffuse meters into the regolith. As a result, significant methane may be temporarily lost to the regolith on a seasonal time scale. As this weak adsorption is fully reversible, methane will be re-released into the atmosphere when surface and subsurface temperatures rise and so no net loss of methane occurs. Heterogeneous interaction of methane with martian soil grains is the only process proposed thus far which contains both rapid methane loss and rapid methane production mechanisms and is thus fully consistent with the reported variability of methane on Mars. 相似文献
2.
In this paper we attempt to answer the question, how formation of a small-scale trench in the martian regolith affects local distribution of the subsurface ice. We are especially interested in the consequences of digging a trench to search for buried ice, as has been done during the Phoenix Mars Lander mission. However, the results may be also applicable for natural troughs, or cracks. We present results of simulations of diurnal exchange of water between the regolith and the atmosphere. Our model includes the heat and vapor migration in the regolith surrounding the trench, as well as formation of diurnal frost. We take into account scattering of light in the atmosphere and on the trench facets, as well as changes of atmospheric humidity on diurnal and seasonal time scales. Our calculations show, that the measurements of ice content in a sample obtained within one, or two days from the beginning of digging should not be affected. However, on somewhat longer time scale at the south facing site of the trench the regolith can be significantly depleted from ice. This effect should be taken into account if the excavation and taking samples from different depths will be performed in stages separated in time by a month, or more. 相似文献
3.
Bruce M. Jakosky 《Icarus》1983,55(1):19-39
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. 相似文献
4.
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. 相似文献
5.
A 1-D collisional Monte Carlo model of Europa's atmosphere is described in which the sublimation and sputtering sources of H2O molecules and their molecular fragments are accounted for as well as the radiolytically produced O2. Dissociation and ionization of H2O and O2 by magnetospheric electron, solar UV-photon and photo-electron impact, and collisional ejection from the atmosphere by the low-energy plasma are taken into account. Reactions with the surface are discussed, but only adsorption and atomic oxygen recombination are included in this model. The size of the surface-bounded oxygen atmosphere of Europa is primarily determined by a balance between atmospheric sources from irradiation of the satellite's icy surface by the high-energy magnetospheric charged particles and atmospheric losses from collisional ejection by the low-energy plasma, photo- and electron-impact dissociation, and ionization and pick-up from the surface-bounded atmosphere. A range of sources rates for O2 to H2O are used with a larger oxygen-to-water ratio than suggested by laboratory measurements in order to account for differences in adsorption onto grains in the regolith. These calculations show that the atmospheric composition is determined by both the water and oxygen photochemistry in the near-surface region, escape of suprathermal oxygen and water into the jovian system, and the exchange of radiolytic water products with the porous regolith. For the electron impact ionization rates used, pick-up ionization is the dominant oxygen loss process, whereas photo-dissociation and atmospheric sputtering are the dominant sources of neutral oxygen for Europa's neutral torus. Including desorption and loss of water enhances the supply of oxygen species to the neutral torus, but hydrogen produced by radiolysis is the dominant source of neutrals for Europa's torus in these models. 相似文献
6.
This paper describes General Circulation Model (GCM) simulations of the martian water cycle focusing on the effects of an adsorbing regolith. We describe the 10-layer regolith model used in this study which has been adapted from the 1-D model developed by Zent, A.P., Haberle, R.M., Houben, H.C., Jakosky, B.M. [1993. A coupled subsurface-boundary layer model of water on Mars. J. Geophys. Res. 98 (E2), 3319-3337, February]. Even with a 30-min timestep and taking into account the effect of surface water ice, our fully implicit scheme compares well with the results obtained by Zent, A.P., Haberle, R.M., Houben, H.C., Jakosky, B.M. [1993. A coupled subsurface-boundary layer model of water on Mars. J. Geophys. Res. 98 (E2), 3319-3337, February]. This means, however, that the regolith is not able to reproduce the diurnal variations in column water vapour abundance of up to a factor of 2-3 as seen in some observations, with only about 10% of the atmospheric water vapour column exchanging with the subsurface on a daily basis. In 3-D simulations we find that the regolith adsorbs water preferentially in high latitudes. This is especially true in the northern hemisphere, where perennial subsurface water ice builds up poleward of 60° N at depths which are comparable to the Odyssey observations. Much less ice forms in the southern high latitudes, which suggests that the water ice currently present in the martian subsurface is not stable under present conditions and is slowly subliming and being deposited in the northern hemisphere. When initialising the model with an Odyssey-like subsurface water ice distribution the model is capable of forcing the simulated water cycle from an arbitrary state close to the Mars Global Surveyor Thermal Emission Spectrometer observations. Without the actions of the adsorbing regolith the equilibrated water cycle is found to be a factor of 2-4 too wet. The process by which this occurs is by adsorption of water during northern hemisphere summer in northern mid and high latitudes where it remains locked in until northern spring when the seasonal CO2 ice cap retreats. At this time the water diffuses out of the regolith in response to increased temperature and is returned to the residual water ice cap by eddie transport. 相似文献
7.
We have studied the sublimation of ice and water vapor transport through various thicknesses of clay (<63 μm grain size). We experimentally demonstrate that both adsorption and diffusion strongly affect the transport of water, and that the processes of diffusion and adsorption can be separately quantified once the system comes to a steady state. At shallow depths of clay, water vapor transport is determined by diffusion through both the atmosphere and the clay layer, whereas at greater depth the rate of sublimation of the ice is governed only by diffusion through the clay. Using two different models, we determine the diffusion coefficient for water vapor through unconsolidated clay layer to be 1.08±0.04×10−4 and . We also determined the adsorption isotherms for the clay layer, which follow the Langmuir theory at low water vapor pressure (<100 Pa, where a monolayer of water molecules forms on the surface of the clay) and the BET theory at higher pressure (where multiple water layers form). From our analysis of both types of isotherms we determined the adsorption constants to be and c=30±10, respectively, and specific surface areas of 1.10±0.2×105 and , respectively. Finally, we report a theoretical kinetic model for the simultaneous diffusion and adsorption from which we determine adsorption kinetic constants according to the Langmuir theory of and . If the martian regolith possesses diffusive properties similar to those of the unconsolidated montmorillonite soil we investigated here, it would not represent a significant barrier to the sublimation of subsurface ice. However, at the low subsurface temperatures of high latitude (180 K on average), ice could survive from the last glaciation period (about 300 to 400,000 years ago). Higher subsurface temperatures in the equatorial regions would prevent long-timescale survival of ice in the shallow subsurface. In agreement with previous work, we show that adsorption of water by a clay regolith could provide a significant reservoir of subsurface water and it might account for the purported diurnal cycle in the water content of the atmosphere. 相似文献
8.
《Planetary and Space Science》2007,55(10):1246-1256
Small amounts of methane have been detected in the atmosphere of Mars, though the actual sources of the gas remain unknown. Thermodynamic conditions on Mars suggest that gas clathrate hydrate deposits might exist at the polar caps and in some areas of the planetary subsurface. We review the literature available on the detection of methane in the martian atmosphere and the presence of gas clathrate hydrates on Mars. The possibility of martian methane clathrate deposits is established, and initial sources for the sequestered methane are discussed. Based on correlated data and information from disparate sources, we conclude that subsurface methane clathrate deposits are a possible immediate source for the observed atmospheric methane on Mars. 相似文献
9.
Titan is the only body, other than the Earth where liquid is present on the surface. In the present work we consider behavior of methane in the pores of Titan's regolith. Using numerical model we investigate quantitative conditions necessary for the onset of convection. We have found that the methane convection in Titan's regolith is possible. It can be expected in regions where the regolith has sufficiently high porosity, independently of the geothermal heat flux. 相似文献
10.
Assessment of a 2016 mission concept: The search for trace gases in the atmosphere of Mars 总被引：1，自引：0，他引：1
Richard W. Zurek Augustin Chicarro Mark A. Allen Jean-Loup Bertaux R.Todd Clancy Frank Daerden Vittorio Formisano James B. Garvin Gerhard Neukum Michael D. Smith 《Planetary and Space Science》2011,59(2-3):284-291
The reported detection of methane in the atmosphere of Mars as well as its potentially large seasonal spatial variations challenge our understanding of both the sources and sinks of atmospheric trace gases. The presence of methane suggests ongoing exchange between the subsurface and the atmosphere of potentially biogenic trace gases, while the spatial and temporal variations cannot be accounted for with current knowledge of martian photochemistry. A Joint Instrument Definition Team (JIDT) was asked to assess concepts for a mission that might follow up on these discoveries within the framework of a series of joint missions being considered by ESA and NASA for possible future exploration of Mars. The following is based on the report of the JIDT to the space agencies (Zurek et al., 2009); a synopsis of the report was presented at the Workshop on Mars Methane held in Frascati, Italy, in November 2009. To summarize, the JIDT believed that a scientifically exciting and credible mission could be conducted within the evolving capabilities of the science/telecommunications orbiter being considered by ESA and NASA for possible launch in the 2016 opportunity for Mars. 相似文献
11.
R.V. Gough J.J. Turley G.R. Ferrell K.E. Cordova S.E. Wood D.O. DeHaan C.P. McKay O.B. Toon M.A. Tolbert 《Planetary and Space Science》2011,59(2-3):238-246
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. 相似文献
12.
Eric Chassefière 《Icarus》2009,204(1):137-271
The observations of methane made by the PFS instrument onboard Mars Express exhibit a definite correlation between methane mixing ratio, water vapor mixing ratio, and cloud optical depth. The recent data obtained from ground-based telescopes seem to confirm the correlation between methane and water vapor. In order to explain this correlation, we suggest that the source of gaseous methane is atmospheric, rather than at the solid surface of the planet, and that this source may consist of metastable submicronic particles of methane clathrate hydrate continuously released to the atmosphere from one or several clathrate layers at depth, according to the phenomenon of “anomalous preservation” evidenced in the laboratory. These particles, lifted up to middle atmospheric levels due to their small size, and therefore filling the whole atmosphere, serve as condensation nuclei for water vapor. The observed correlation between methane and water vapor mixing ratios could be the signature of the decomposition of the clathrate crystals by condensation-sublimation processes related to cloud activity. Under the effect of water condensation on crystal walls, metastability could be broken and particles be eroded, resulting in a subsequent irreversible release of methane to the gas phase. Using PFS data, and according to our hypothesis, the lifetime of gaseous methane is estimated to be smaller than an upper limit of 6 ± 3 months, much smaller than the lifetime of 300 yr calculated from atmospheric chemical models. The reason why methane has a short lifetime might be the occurrence of heterogeneous chemical decomposition of methane in the subsurface, where it is known since Viking biology experiments that oxidants efficiently decompose organic matter. If true, it is shown by using existing models of H2O2 penetration in the regolith that methane could prevent H2O2 from penetrating in the subsurface, and further oxidizing the soil, at depths larger than a few millimeters. The present source of methane clathrate, acting over the last few hundred thousand or million years, could have given rise to the thin CO2-ice layer covering the permanent water ice south polar cap. The hypothesis proposed in this paper requires, to be validated, a number of laboratory experiments studying the stability of methane clathrates in martian atmospheric conditions, and the kinetics and amplitude of clathrate particle erosion in presence of condensing water vapor. Detailed future observations of methane, and associated modeling, will allow to more accurately quantify the production rate of methane clathrate, its temporal variability at seasonal scale, and possibly to locate the source(s) of clathrates at the surface. 相似文献
13.
Caroline Thomas Olivier Mousis Sylvain Picaud Vincent Ballenegger 《Planetary and Space Science》2009,57(1):42-47
Recent observations have evidenced traces of methane (CH4) heterogeneously distributed in the martian atmosphere. However, because the lifetime of CH4 in the atmosphere of Mars is estimated to be around 300-600 years on the basis of photochemistry, its release from a subsurface reservoir or an active primary source of methane have been invoked in the recent literature. Among the existing scenarios, it has been proposed that clathrate hydrates located in the near subsurface of Mars could be at the origin of the small quantities of the detected CH4. Here, we accurately determine the composition of these clathrate hydrates, as a function of temperature and gas phase composition, by using a hybrid statistical thermodynamic model based on experimental data. Compared to the other recent works, our model allows us to calculate the composition of clathrate hydrates formed from a more plausible composition of the martian atmosphere by considering its main compounds, i.e. carbon dioxide, nitrogen and argon, together with methane. Besides, because there is no low temperature restriction in our model, we are able to determine the composition of clathrate hydrates formed at temperatures corresponding to the extreme ones measured in the polar caps. Our results show that methane enriched clathrate hydrates could be stable in the subsurface of Mars only if a primitive CH4-rich atmosphere has existed or if a subsurface source of CH4 has been (or is still) present. 相似文献
14.
It has been suggested that the present release rate of methane to the Martian atmosphere could be the result of serpentinization in the deep subsurface, followed by the conversion of H2 to CH4 in a CO2-rich fluid. Making this assumption, we show that the cryosphere could act as a buffer storing, under the form of micron-size methane clathrate particles, the methane delivered from below by hydrothermal fluids and progressively releasing it to the atmosphere at the top. From an extrapolation of the present CH4 release rate back to the past, we calculate that up to several hundred millibars (～200–2000 mbar) of CO2, resulting from the oxidation of the released CH4, in addition to the volcanic supply (～400 mbar), should have accumulated in the atmosphere in the absence of a CO2 sink. We reassess the capability of escape to have removed CO2 from the atmosphere by C non-thermal escape and show that it is not significant. We suggest that atmospheric carbon is recycled to the crust through an active subsurface hydrological system, and precipitates as carbonates within the crust. During episodic periods of magmatic activity, these carbonates are decomposed to CO2 dissolved in running water, and CO2 can react with H2 formed by serpentinization to build CH4. CH4 is then buffered in the subsurface cryosphere, above the water table, and finally released to the atmosphere, before being recycled to the subsurface hydrological system, and converted back to carbonates. We propose a typical evolution curve of the CO2 pressure since the late Noachian based on our hypothesis. Contrary to the steady state carbon cycle at work on Earth, a progressive damping of the carbon cycle occurs on Mars due to the absence of plate tectonics and the progressive cooling of the planet. 相似文献
15.
《Icarus》1987,71(2):241-249
We report new CO2 adsorption measurements on palagonites. These results are used together with earlier results on basalt and nontronite adsorption to derive a “generic” relationship which is valid to within a factor of 3 for likely mixtures of basalt and weathering products of basalt. The relationship involves only t, PCO2, and the specific surface area, and is relatively insensitive to mineralogy. It is used to predict the distribution and exchange of CO2 on Mars. We conclude: (1) One to two orders of magnitude more CO2 is adsorbed on the regolith than is present in the atmosphere and cap. (2) Nonetheless, most of the initially degassed CO2 must have been lost to space or must be present as carbonates, especially if there was enough degassed CO2 to provide a significant early greenhouse effect. (3) Given the derived relationship, the CO2 vapor pressure curve, and the constraint that the system exhibits the current PCO2 at the current obliquity, it is possible to predict approximately the atmospheric pressure at any obliquity (with or without a cap) without knowing the total available CO2 inventory, the regolith mass, the regolith distribution, or its mineralogy, any better than those parameters are currently known. 相似文献
16.
《Icarus》1986,67(1):1-18
A thermal/diffusive model of H2O kinetics and equilibrium was developed to investigate the long-term evolution and depth distribution of subsurface ice on Mars. The model quantitatively takes into account (1) obliquity variations; (2) eccentricity variations; (3) long-term changes in the solar luminosity; (4) variations in the argument of subsolar meridian (in planetocentric equatorial coordinates); (5) albedo changes at higher latitudes due to seasonal phase changes of CO2 and the varying extent of CO2 ice cover; (6) planetary internal heat flow; (7) temperature variations in the regolith as a function of depth, time, and latitude due to the above factors; (8) atmospheric pressure variations over a 104-year time scale; (9) the effects of factors (1) through (5) on seasonal polar cap temperatures; and (10) Knudsen and molecular diffusion of H2O through the regolith. The migration of H2O into or out of the regolith is determined by two boundary conditions, the H2O vapor pressure at the subsurface ice boundary and the annual average H2O concentration at the base of the atmosphere. These are controlled respectively by the annual average regolith temperature at the given depth and seasonal temperatures at the polar cap. Starting from an arbitrary initial uniform depth distribution of subsurface ice, H2O fluxes into or out of the regolith are calculated for 100 selected obliquity cycles, each representing a different epoch in Mars' history. The H2O fluxes are translated into ice thicknesses and extrapolated over time to give the subsurface ice depth as a function of latitude and time. The results show that obliquity variations influence annual average regolith temperatures in varying degrees, depending on latitude, with the greatest effect at the poles and almost no effect at 40° lat. Insolation changes at the pole, due to obliquity, argument of subsolar meridian, and eccentricity variations can produce enormous atmospheric H2O concentration variations of ≈6 orders of magnitude over an obliquity cycle. Superimposed on these cyclic variations is a slow, monotonic change due to the increasing solar luminosity. Albedo changes at the polar cap due to seasonal phase changes of CO2 and the varying thickness of the CO2 ice cover are critically important in determining annual average atmospheric H2O concentrations. Despite the strongly oscillating character of the boundary conditions, only small amounts of H2O are exchanged between the regolith and the atmosphere per obliquity cycle (<10 g/cm2). The net result of H2O migration is that the regolith below 30–40° lat is depleted of subsurface ice, while the regolith above 30–40° lat contains permanent ice due to the depth of penetration of the annual thermal wave. This result is supported by recent morphological studies. The rate of migration of H2O is strongly dependent on average pore/capillary radius for which we have assumed values of 1 and 10 μm. We estimate that the H2O ice removed from the regolith would produce a permanent ice cap with a volume between 2 × 106 and 6 × 106 km3. This generally agrees with estimates deduced from deflationary features at lower latitudes, depositional features at higher latitudes, and the mass of the polar caps. 相似文献
17.
Sarah K. Noble Lindsay P. Keller Carl M. Pieters 《Meteoritics & planetary science》2005,40(3):397-408
Abstract— We have analyzed a suite of lunar regolith breccias in order to assess how well space weathering products can be preserved through the lithification process and therefore whether or not it is appropriate to search for space weathering products in asteroidal regolith breccia meteorites. It was found that space weathering products, vapor/sputter deposited nanophase‐iron‐bearing rims in particular, are easily identified in even heavily shocked/compacted lunar regolith breccias. Such rims, if created on asteroids, should thus be preserved in asteroidal regolith breccia meteorites. Two additional rim types, glass rims and vesicular rims, identified in regolith breccias, are also described. These rims are common in lunar regolith breccias but rare to absent in lunar soils, which suggests that they are created in the breccia‐forming process itself. While not “space weathering products” in the strictest sense, these additional rims give us insight into the regolith breccia formation process. The presence or absence of glass and/or vesicular rims in asteroidal regolith breccias will likewise tell us about environmental conditions on the surface of the asteroid body on which the breccia was created. 相似文献
18.
The inversion of regolith thickness over the nearside hemisphere of the Moon from newly acquired Earth-based 70-cm Arecibo radar data is investigated using a quantitative radar scattering model. The radar scattering model takes into account scattering from both the lunar surface and buried rocks in the lunar regolith, and three parameters are critically important in predicting the radar backscattering coefficient: the dielectric constant of the lunar regolith, the surface roughness, and the size and abundance of subsurface rocks. The measured dielectric properties of the Apollo regolith samples at 450 MHz are re-analyzed, and an improved relation among the complex dielectric constant, bulk density and regolith composition is obtained. The complex dielectric constant of the lunar regolith is estimated globally from this relation using the regolith composition derived from Lunar Prospector gamma-ray spectrometer data. To constrain the lunar surface roughness and abundance of subsurface rocks from radar data, nine regions are selected as calibration sites where the regolith thickness has been estimated using independent analysis techniques. For these sites, scattering from the lunar surface and buried rocks cannot be perfectly distinguished, and a tradeoff relationship exists between the size and abundance of buried rocks and surface roughness. Using these tradeoff relations as guidelines for globally representative parameters, the regolith thickness of four regions over the lunar nearside is inverted, and the inversion uncertainties caused by calibration errors of the radar data and model input parameters are analyzed. The regolith thickness of the maria is generally smaller than that of highlands, and older surfaces have thicker regolith thicknesses. Our approach cannot be applied to regions where the surface roughness is very high, such as with young rocky craters and regions in the highly rugged highlands. 相似文献
19.
We have developed a 1D thermal model of Mercury's regolith, in order to simulate the heat diffusion in the upper subsurface (first 10 m). We assume in our model that the thermophysical properties of the Hermean regolith are similar to those of the lunar regolith. We apply our thermal model to the Caloris basin which slopes induce distortions of the surface temperature compared to results obtained for a perfect spherical planet. This thermal model is then coupled with a 3D Monte Carlo model of Mercury's sodium exosphere [Leblanc, F., Johnson, R.E., 2003. Icarus 164, 261-281; Leblanc, F., Delcourt, D., Johnson, R.E., 2003b. J. Geophys. Res. 108 (E12), doi:10.1029/2003JE002151/.5136], in order to describe the signatures of Caloris basin on Mercury's sodium exosphere in term of temporal and spatial variabilities. In particular, we find a motion of the maxima of sodium density in the exosphere towards the Northern hemisphere similar to the one observed by Potter et al. [Potter, A.E., Morgan, T.H., Killen, R.M., 1999. Planet. Space Sci., 47, 1441-1449] but did not reproduce the observed change of the emission brightness. The main conclusion of this study is that the Caloris basin-exosphere relations might be observable from the Earth which we hope will motivate new observations of Mercury's exosphere. 相似文献
20.
Tetsuya Tokano 《Icarus》2003,164(1):50-78
In an effort to test and to understand the global hydrogen distribution in the shallow subsurface of Mars retrieved by the Mars Odyssey gamma-ray spectrometer, the present state and movement of water are investigated by a coupled global subsurface-atmosphere water cycle model. It was found that the observed global subsurface hydrogen distribution is largely consistent with the modeled global water cycle, so a large fraction of hydrogen is likely to exist as water, at low and mid latitudes in the form of adsorbed water. Under the present climate the water content in the shallow subsurface becomes higher in the northern hemisphere than in the southern hemisphere as a result of global water cycle, regardless of the initial water distribution in the soil or adsorptive capacity. The higher annual maximum soil temperature in the south, stronger net northward transport of atmospheric water vapor, and the emission of vapor from the northern residual polar cap in northern summer contribute to this hemispheric asymmetry. The generally higher adsorptive capacity of clay minerals in the northern plains may further increase this bias. The longitudinal inhomogeneity is caused by several factors, such as thermal inertia, adsorptive capacity, and atmospheric surface pressure. The water abundance is locally high in low thermal inertia regions (e.g., Arabia Terra) and at deep places where the surface pressure is high (e.g., Hellas); it is low in soil with a low adsorptive capacity (e.g., Tharsis) and high thermal inertia regions (e.g., Solis Planum). Most of the soil humidity near the surface at low and mid latitudes may originate from the atmosphere. The model implies that the upper soil layer should be largely ice-free because otherwise an excessive sublimation and vapor emission into the atmosphere in warm seasons would violate the observational constraints. Moreover, the more uniform latitudinal variation of the observed hydrogen abundance near the surface compared to that of deeper layers is indicative of the presence of adsorbed water instead of ground ice because the adsorbed water content does not as steeply depend on latitude as the ground ice stability. Concerning the regolith mineralogy, montmorillonite can much better account for the observed water cycle than palagonite. While the presence of permanent ground ice appears likely in the polar region below a thin layer, large seasonal cycle of phase change between pore ice and adsorbed water may be possible. Regolith adsorption/desorption is neither negligible nor crucial for the seasonal atmospheric water cycle, but the surface-atmosphere coupling is a major prerequisite for the long-term evolution of subsurface water distribution. 相似文献