Oxygen and carbon isotope ratios in the martian atmosphere

Oxygen and carbon isotope ratios in the martian CO₂ are key values to study evolution of volatiles on Mars. The major problems in spectroscopic determinations of these ratios on Mars are uncertainties associated with: (1) equivalent widths of the observed absorption lines, (2) line strengths in spectroscopic databases, and (3) thermal structure of the martian atmosphere during the observation. We have made special efforts to reduce all these uncertainties. We observed Mars using the Fourier Transform Spectrometer at the Canada–France–Hawaii Telescope. While the oxygen and carbon isotope ratios on Mars were byproducts in the previous observations, our observation was specifically aimed at these isotope ratios. We covered a range of 6022 to 6308 cm⁻¹ with the highest resolving power of ν/δν=3.5×10⁵ and a signal-to-noise ratio of 180 in the middle of the spectrum. The chosen spectral range involves 475 lines of the main isotope, 184 lines of ¹³CO₂, 181 lines of CO¹⁸O, and 119 lines of CO¹⁷O. (Lines with strengths exceeding 10⁻²⁷ cm at 218 K are considered here.) Due to the high spectral resolution, most of the lines are not blended. Uncertainties of retrieved isotope abundances are in inverse proportion to resolving power, signal-to-noise ratio, and square root of the number of lines. Laboratory studies of the CO₂ isotope spectra in the range of our observation achieved an accuracy of 1% in the line strengths. Detailed observations of temperature profiles using MGS/TES and data on temperature variations with local time from two GCMs are used to simulate each absorption line at various heights in each part of the instrument field of view and then sum up the results. Thermal radiation of Mars' surface and atmosphere is negligible in the chosen spectral range, and this reduces errors associated with uncertainties in the thermal structure on Mars. Using a combination of all these factors, the highest accuracy has been achieved in measuring the CO₂ isotope ratios: ¹³C/¹²C = 0.978 ± 0.020 and ¹⁸O/¹⁶O = 1.018 ± 0.018 times the terrestrial standards. Heavy isotopes in the atmosphere are enriched by nonthermal escape and sputtering, and depleted by fractionation with solid-phase reservoirs. The retrieved ratios show that isotope fractionation between CO₂ and oxygen and carbon reservoirs in the solid phase is almost balanced by nonthermal escape and sputtering of O and C from Mars.     

Electron reflectometry in the martian atmosphere

The technique of electron reflectometry, a method for remote estimation of planetary magnetic fields, is expanded from its original use of mapping crustal magnetic fields at the Moon to achieving the same purpose at Mars, where the presence of a substantial atmosphere complicates matters considerably. The motion of solar wind electrons, incident on the martian atmosphere, is considered in detail, taking account of the following effects: the electrons' helical paths around the magnetic field lines to which they are bound, the magnetic mirror force they experience due to converging field lines in the vicinity of crustal magnetic anomalies, their acceleration/deceleration by electrostatic potentials, their interactions with thermal plasma, their drifts due to magnetic field line curvature and perpendicular electric fields and their scattering off, and loss of energy through a number of different processes to, atmospheric neutrals. A theoretical framework is thus developed for modeling electron pitch angle distributions expected when a spacecraft is on a magnetic field line which is connected to both the martian crust and the interplanetary magnetic field. This framework, along with measured pitch angle distributions from the Mars Global Surveyor (MGS) Magnetometer/Electron Reflectometer (MAG/ER) experiment, can be used to remotely measure crustal magnetic field magnitudes and atmospheric neutral densities at ∼180 km above the martian datum, as well as estimate average parallel electric fields between 200 and 400 km altitude. Detailed analysis and full results, concerning the crustal magnetic field and upper thermospheric density of Mars, are left to two companion papers.     

Recombination rates of O and CO on solid CO2: Implications for the composition of the martian atmosphere

An atomic oxygen flow system and a C¹⁴ radiochemical technique have been used to show that the reactions O + CO → CO₂ and O + O → O₂, are heterogeneously catalysed by solid CO₂ at 77 K.The O-CO recombination is first order in CO and inhibited by O, whereas the O-O recombination is first order in O and weakly inhibited by CO. Assuming simple first order kinetics, recombination coefficients γ_co = 1.3(±0.9) × 10^?5 and γ_O = 0.05± 0.02 are determined. A recombination mechanism involving an intermediate adsorbed CO₃ is proposed. If the kinetic results are assumed to apply under Martian surface conditions, then conversion of CO to CO₂ by reaction on the solid CO₂ at the polar caps occurs at ~10 times the total column recombination rates for homogeneous reactions previously proposed; night-side CO₂ ice clouds would also constitute an important recombination surface.     

Convective instability in the martian middle atmosphere

Dry convective instabilities in Mars’s middle atmosphere are detected and mapped using temperature retrievals from Mars Climate Sounder observations spanning 1.5 martian years. The instabilities are moderately frequent in the winter extratropics. The frequency and strength of middle atmospheric convective instability in the northern extratropics is significantly higher in MY 28 than in MY 29. This may have coupled with changes to the northern hemisphere mid-latitude and tropical middle atmospheric temperatures and contributed to the development of the 2007 global dust storm. We interpret these instabilities to be the result of gravity waves saturating within regions of low stability created by the thermal tides. Gravity wave saturation in the winter extratropics has been proposed to provide the momentum lacking in general circulation models to produce the strong dynamically-maintained temperature maximum at 1-2 Pa over the winter pole, so these observations could be a partial control on modeling experiments.     

Physical parameters of the martian atmosphere

The following physical parameters have been computed from 0 to 200 km altitude; (1) pressure, (2) density (3), speed of sound, (4) density, (5) number density, (6) mean free path, (7) viscosity, (8) pressure scale, (9) mean particle velocity, (10) collisional frequency and (11) columnar mass.The Viking measurements have been used as input data. A critical comparison of the computed pressures and densities, is given, useful for future explorations.     

A sensitive search for SO2 in the martian atmosphere: Implications for seepage and origin of methane

Mars was observed near the peak of the strongest SO₂ band at 1364-1373 cm⁻¹ with resolving power of 77,000 using the Texas Echelon Cross Echelle Spectrograph on the NASA Infrared Telescope Facility. The observation covered the Tharsis volcano region which may be preferable to search for SO₂. The spectrum shows absorption lines of three CO₂ isotopomers and three H₂O isotopomers. The water vapor abundance derived from the HDO lines assuming D/H = 5.5 times the terrestrial value is 12±1.0 pr. μm, in agreement with the simultaneous MGS/TES observations of 14 pr. μm at the latitudes (50° S to 10° N) of our observation. Summing of spectral intervals at the expected positions of sixteen SO₂ lines puts a 2σ upper limit on SO₂ of 1 ppb. SO₂ may be emitted into the martian atmosphere by seepage and is removed by three-body reactions with OH and O. The SO₂ lifetime, 2 years, is longer than the global mixing time 0.5 year, so SO₂ should be rather uniformly distributed across Mars. Seepage of SO₂ is less than 15,000 tons per year on Mars which is smaller than the volcanic production of SO₂ on the Earth by a factor of 700. Because CH₄/SO₂ is typically 10⁻⁴-10⁻³ in volcanic gases on the Earth, our results show seepage is unlikely to be the source of the recently discovered methane on Mars and therefore strengthen its biogenic origin.     

Fractionated martian atmosphere in the nakhlites?

Abstract— Considerable evidence points to a martian origin of the SNC meteorites. Noble gas isotopic compositions have been measured in most SNC meteorites. The ¹²⁹Xe/¹³²Xe vs. ⁸⁴Kr/¹³²Xe ratios in Chassigny, most shergottites, and lithology C of EETA 79001 define a linear array. This array is thought to be a mixing line between martian mantle and martian atmosphere. One of the SNC meteorites, Nakhla, contains a leachable component that has an elevated ¹²⁹Xe/¹³²Xe ratio relative to its ⁸⁴Kr/¹³²Xe ratio when compared to this approximately linear array. The leachable component probably consists in part of iddingsite, an alteration product produced by interaction of olivine with aqueous fluid at temperatures lower than 150 °C. The elevated Xe isotopic ratio may represent a distinct reservoir in the martian crust or mantle. More plausibly, it is elementally fractionated martian atmosphere. Formation of sediments fractionates the noble gases in the correct direction. The range of sediment/atmosphere fractionation factors is consistent with the elevated ¹²⁹Xe/¹³²Xe component in Nakhla being contained in iddingsite, a low temperature weathering product. The crystallization age of Nakhla is 1.3 Ga. Its low-shock state suggests that it was ejected from near the surface of Mars. As liquid water is required for the formation of iddingsite, these observations provide further evidence for the near surface existence of aqueous fluids on Mars more recently than 1.3 Ga.     

Experimental hydrothermal alteration of a martian analog basalt: Implications for martian meteorites

Abstract— A number of martian meteorite samples contain secondary alteration minerals such as Ca‐Mg‐Fe carbonates, Fe oxides, and clay minerals. These mineral assemblages hint at hydrothermal processes occurring in the martian crust, but the alteration conditions are poorly constrained. This study presents the results of experiments that examined the alteration of a high‐Fe basalt by CO₂‐saturated aqueous fluids at 23 and 75 °C and by mixed H₂O‐CO₂ vapors at 200 and 400 °C and water‐rock ratios of 1:1 and 1:10. Results indicate that observable alteration of the basalt takes place after runs of only seven days. This alteration includes mobilization of silica into phases such as opal‐CT and quartz, as well as the formation of carbonates, oxides, and at some conditions, zeolites and hydrous silicates. The degree of alteration increases with run temperature and, in high‐temperature vapor experiments, with increasing water content of the vapor. The degree of alteration and the mineralogy observed in the martian meteorites suggests that none of these samples were exposed to aqueous fluids for long periods of time. Nakhla and Lafayette probably interacted with water for relatively brief periods of time; if so, silica may have been leached from the parent rocks by the altering fluids. Allan Hills 84001 shows possible evidence for very limited interaction with an aqueous fluid, but the overall slight degree of alteration described for this meteorite strongly suggests that it never interacted extensively or at high temperature with any water‐bearing fluid. Elephant Moraine A79001 may not have been altered by aqueous fluids at all. The results of this study best support models wherein the meteorite parent rocks were wetted intermittently or for brief periods of time rather than models that invoke long‐term reaction with large volumes of water. Our experiments studied alteration of a high‐Fe basalt by dilute, CO₂‐saturated, aqueous solutions at 23 and 75 °C and by mixed H₂O‐CO₂ vapors at 200 and 400 °C. The results suggest that alteration of the parent rock takes place even after very short reaction times of seven days. All experiments produced carbonate minerals, including calcite, and in some cases, magnesite, siderite, and ankerite. A free silica phase, either opal, quartz, or hydrated silica, formed in most experiments. More altered experiments also contained minerals such as zeolites and hydrous phyllosilicates. Clay minerals were not observed to form in any experiments. In aqueous fluids, higher temperature corresponded with a higher degree of alteration, whereas changing fluid composition had no observable effect. In high‐temperature vapors, the degree of alteration was controlled by temperature and the proportion of H₂O to CO₂, with water‐rock ratio also playing a role in transport of silica. Application of these results to martian meteorites that contain secondary alteration minerals suggests that none of the martian rocks underwent extensive interaction with aqueous fluids. Nakhla and Lafayette contain clay minerals, which suggests that they interacted with water to some extent, possibly at elevated temperatures. Although ALH84001 shows possible evidence of very limited interaction with aqueous fluids, EETA79001 does not. These results support models for the alteration of these meteorites that do not invoke long‐term interaction with water or reaction with large volumes of water. Except for some models for alteration of ALH84001, this conclusion agrees with most of the literature on alteration of martian meteorites.     

Methane adsorption on a martian soil analog: An abiogenic explanation for methane variability in the martian atmosphere

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.     

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.     

Isotopic fractionation of methane in the martian atmosphere

The existence of methane in the martian atmosphere may be an indicator of subsurface life. Biological processes are known to fractionate the common isotopologues of methane, and hence measuring these isotopic ratios may yield constraints on the nature of the methane source. Any measurement of the isotopic ratios of atmospheric methane must consider the additional fractionation due to photochemistry in order to quantify the isotopic ratios of the source. Using a one-dimensional photochemical model, we find that photochemistry has a small (4.5‰) contribution to δ¹³C(CH₄) but has a large (114‰) contribution to δD(CH₄). Confirmation of these fractionation values will require additional laboratory data on key model inputs, particularly the ultraviolet absorption cross sections of ¹³CH₄ and kinetic rate coefficients for the reactions of ¹³CH₄ and CH₃D with OH and O(¹D) at pressures and temperatures relevant to the martian atmosphere.     

Hydrogen‐isotopic compositions in Allan Hills 84001 and the evolution of the martian atmosphere

Abstract— Hydrogen‐isotopic compositions of carbonate and maskelynite in Allan Hills (ALH) 84001 were measured by secondary ion mass spectrometry (SIMS). the δd values of both minerals show considerable deviation. The deviation seems to be caused by addition of varying amounts of terrestrial water in the case of carbonate. In the case of maskelynite, H is heterogeneously distributed and the deviation in δD values seems to be due to mixing of this indigenous heavy H with isotopically normal H present in the SIMS chamber. The indigenous δD value in ALH 84001 seems to be ～2000%‰. Carbonate rather than maskelynite seems to be the main carrier of H in ALH 84001. Because ALH 84001 is ～4 Ga old, the H‐isotopic composition suggests that a large fraction of the initial martian atmosphere had already escaped by 4 Ga.     

Thermal alteration of nontronite and montmorillonite: Implications for the martian surface

To test the effects of meteorite impacts on martian phyllosilicate deposits, we heated two smectites (nontronite and montmorillonite) to temperatures ranging from 350 °C to 1150 °C for durations of 4-24 h in two different atmospheres, under air and a steady flow of CO₂. Samples were analyzed using X-ray diffraction (XRD) and near-infrared (NIR) and mid-infrared (MIR) reflectance spectroscopy. Interlayer water was lost after heating to temperatures of ∼400 °C. Between 400 °C and 700 °C, nontronite converted to an intermediary phase which conserved the XRD pattern of untreated nontronite with the exception of the 0 0 1 peak. Nanocrystalline high-temperature phases formed for both smectites at temperatures between 700 °C and 1000 °C. Finally, after being heated to temperatures above ∼1100 °C, the samples melted and recrystallized into secondary phases. Secondary high-temperature phases included sillimanite and cristobalite for both smectites plus hematite for nontronite. NIR and MIR reflectance spectra significantly evolved with increasing temperature. NIR spectra of smectites showed that 1.4 and 1.9 μm bands decrease in intensity and disappear above 700 °C. Similarly, the 2.2-2.3 μm metal-OH band showed a decrease in intensity as well as an overall shift towards lower wavelengths (for nontronite) due to the thermal resistance of the Al-OH bond compared to the Fe-OH bond. NIR spectra of montmorillonite showed a gradual increase in band depth up to temperatures between 500 °C and 600 °C, then decreased with increasing temperature. In the MIR spectra of samples heated to temperatures above ∼1100 °C, newly formed bands confirmed the secondary phases identified by XRD. Similarities between the NIR spectra of our heated samples and the phyllosilicates in some martian craters imply that these phyllosilicates were altered by the impact-generated heat and thus were not formed post-impact. In addition, NIR reflectance spectra provide a proxy for shock temperatures of smectites up to 700 °C while MIR is optimum for identification of high-temperature phases of smectites above 700 °C.     

MAWD observations revisited: seasonal behavior of water vapor in the martian atmosphere

Viking/MAWD experiment and more recent MGC/TES observations have provided to date the most detailed information about the annual atmospheric water cycle on Mars. Their data agree in major details but still reveal some disagreements. These disagreements turn out to be most significant in the perihelion season and especially during the major dust storms. We consider the potential influence of aerosol scattering on 1.38 μm water retrieval under various types of observation geometry. In order to obtain new retrievals of water vapor abundance from MAWD data, we apply radiative transfer calculations. The resulting seasonal and spatial distribution of water turns out to be more consistent with TES results, implying a remarkable stability of the martian seasonal water cycle. Mapping data corresponding to particular seasons reveals a distinct wave structure in the global distribution of the water column. We interpret it as a manifestation of a strong control over the water cycle on Mars from the atmospheric circulation.     

History of Martian volatiles: Implications for organic synthesis

A theoretical reconstruction of the history of Martian volatiles indicates that Mars probably possessed a substantial reducing atmosphere at the outset of its history and that its present tenous and more oxidized atmosphere is the result of extensive chemical evolution. As a consequence, it is probable that Martian atmospheric chemical conditions, now hostile with respect to abiotic organic synthesis in the gas phase, were initially favorable. Evidence indicating the chronology and degradational history of Martian surface features, surface mineralogy, bulk volatile content, internal mass distribution, and thermal history suggests that Mars catastrophically developed a substantial reducing atmosphere as the result of rapid accretion. This atmosphere probably persisted—despite the direct and indirect effects of hydrogen escape—for a geologically short time interval during, and immediately following, Martian accretion. That was the only portion of Martian history when the atmospheric environment could have been chemically suited for organic synthesis in the gas phase. Subsequent gradual degrassing of the Martian interior throughout Martian history could not sustain a reducing atmosphere due to the low intensity of planet-wide orogenic activity and the short atmospheric mean residence time of hydrogen on Mars. During the post-accretion history of Mars, the combined effects of planetary hydrogen escape, solar-wind sweeping, and reincorporation of volatiles into the Martian surface produced and maintained the present atmosphere.     

The water cycle in the general circulation model of the martian atmosphere

Within the numerical general-circulation model of the Martian atmosphere MAOAM (Martian Atmosphere: Observation and Modeling), we have developed the water cycle block, which is an essential component of modern general circulation models of the Martian atmosphere. The MAOAM model has a spectral dynamic core and successfully predicts the temperature regime on Mars through the use of physical parameterizations typical of both terrestrial and Martian models. We have achieved stable computation for three Martian years, while maintaining a conservative advection scheme taking into account the water–ice phase transitions, water exchange between the atmosphere and surface, and corrections for the vertical velocities of ice particles due to sedimentation. The studies show a strong dependence of the amount of water that is actively involved in the water cycle on the initial data, model temperatures, and the mechanism of water exchange between the atmosphere and the surface. The general pattern and seasonal asymmetry of the water cycle depends on the size of ice particles, the albedo, and the thermal inertia of the planet’s surface. One of the modeling tasks, which results from a comparison of the model data with those of the TES experiment on board Mars Global Surveyor, is the increase in the total mass of water vapor in the model in the aphelion season and decrease in the mass of water ice clouds at the poles. The surface evaporation scheme, which takes into account the turbulent rise of water vapor, on the one hand, leads to the most complete evaporation of ice from the surface in the summer season in the northern hemisphere and, on the other hand, supersaturates the atmosphere with ice due to the vigorous evaporation, which leads to worse consistency between the amount of the precipitated atmospheric ice and the experimental data. The full evaporation of ice from the surface increases the model sensitivity to the size of the polar cap; therefore, the increase in the latter leads to better results. The use of a more accurate dust scenario changes the model temperatures, which also strongly affects the water cycle.     

Methane evolution from UV-irradiated spacecraft materials under simulated martian conditions: Implications for the Mars Science Laboratory (MSL) mission

Fifteen organic and three inorganic compounds were tested for methane (CH₄) evolution under simulated martian conditions of 6.9 mbar; UVC (200-280 nm) flux of 4 W m⁻²; 20 °C; simulated optical depth of 0.1; and a Mars gas composition of CO₂ (95.3%), N₂ (2.7%), Ar (1.7%), O₂ (0.13%), and water vapor (0.03%). All three inorganic compounds (i.e., NaCl, CaCO₃, graphite) failed to evolve methane at the minimum detection level 0.5 ppm, or above. In contrast, all organic compounds evolved methane when exposed to UV irradiation under simulated martian conditions. The polycyclic aromatic hydrocarbon, pyrene, released the most methane per unit of time at 0.175 nmol CH₄ g⁻¹ h⁻¹, and a spectral reflectance target material used for the MER rovers and Phoenix lander released the least methane at 0.00065 nmol CH₄ cm⁻² h⁻¹. Methane was also released from UV-killed bacterial endospores of Bacillus subtilis. Although all organic compounds evolved methane when irradiated with UV photons under martian conditions, the concentrations of residual organics, biogenic signature molecules, and dead microbial cells should be relatively low on the exterior surfaces of the MSL rover, and, thus, not significant sources of methane contamination. In contrast, kapton tape was found to evolve methane at the rate of 0.00165 nmol CH₄ cm⁻² h⁻¹ (16.5 nmol m⁻² h⁻¹) under the UV and martian conditions tested. Although the evolution of methane from kapton tape was found to decline over time, the large amount of kapton tape used on the MSL rover (lower bound estimated at 3 m²) is likely to create a significant source of terrestrial methane contamination during the early part of the mission.     

The volcanic history of central Elysium Planitia: Implications for martian magmatism

Central Elysium Planitia (CEP) is located south of Elysium Mons. Back to the era of the Viking orbiters, clues accumulated in favor of recent volcanism in relation with ground water release and the formation of long sub-parallel fissures. Four aqueous flood channel systems emanate from linear fissures. Recent eruptions of low viscosity lavas originate from these fissures and from low shield volcanoes. The objective of this paper is to constrain the volcanic history of this region, and to determine the chronological relationships with fluvial/erosional processes. New observations (e.g., new shield volcanoes and one new fluvial event) are summarized on a context map. Thirty-five surfaces have been dated from the count of about 15,000 impact craters. Ages have been cross-checked with relative stratigraphy when possible. A probabilistic approach has been introduced to compare similar ages and define periods of volcanic activity. Our results confirm that some volcanic features are extremely recent (∼2 My). Active periods are found at 2.5-3 My, 4.3 My, 13.5-16.2 My, 19 My, 21-32 My, 58 My, 71 My, 85-95 My, 134 My, 173 My and 234 My, not excluding the possibility that some of the gaps would be filled with additional crater counts. The volcanic activity thus extended for at least the last 250 My. The lava volumes have been estimated from the topographic modeling of the floor of depressions filled up by volcanic products, including the volumes of several large crater cavities buried under lavas (>20% of the total volume). Our new estimation of the total lava volume is 1.5 ± 0.2 × 10⁵ km³. This value corresponds to an average thickness of one hundred meters of lavas for the young volcanic plain. As a consequence, the total eruption rate at CEP, defined as the total volume of lava divided by the time of emplacement 1.4 × 10⁻²-1.8 × 10⁻² m³/s is lower than values typically estimated for terrestrial hot spots or large igneous provinces, suggesting longer inactive periods. The concept of mantle plumes responsible for terrestrial flood volcanism may not be applicable to the case of CEP and the mechanism proposed in Schumacher and Dreuer (2007) offers a plausible alternative to explain our observations.     

A new view of martian evolution

Conventional evolutionary models for Mars adopt a dry mantle solidus. Taking into account the condensation conditions in the preplanetary nebula in the accretion zone of Mars, it can be concluded that large amounts of water or hydrated silicates have condensed in those regions. Therefore, water influences significantly the melting behaviour and the viscosity of the silicatic material. A model for the calculation of the thermal history of a planet is constructed. On this basis, and use of water — saturated solidus — it is possible to derive that the core is not liquid, as given in models employing a dry mantle solidus, but solid to a large extent, which prevents the operation of a large-scale dynamo and explains in that way the lack of a magnetic field. With these assumptions one can construct a possible evolutionary scheme that covers early crust differentiation, a hot thermal past and the missing magnetic field at present.