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1.
CH4 has been observed on Mars both by remote sensing and in situ during the past 15 yr. It could have been produced by early Mars serpentinization processes that could also explain the observed Martian remanent magnetic field. Assuming a cold early Mars, a cryosphere could trap such CH4 as clathrates in stable form at depth. The maximum storage capacity of such a clathrate cryosphere has been recently estimated to be 2 × 1019 to 2 × 1020 moles of methane. We estimate how large amounts of serpentinization‐derived CH4 stored in the cryosphere have been released into the atmosphere during the Noachian and the early Hesperian. Due to rapid clathrate dissociation and photochemical conversion of CH4 to H2, these episodes of massive CH4 release may have resulted in transient H2‐rich atmospheres, at typical levels of 10–20% in a background 1–2 bar CO2 atmosphere. The collision‐induced heating effect of H2 present in such an atmosphere has been shown to raise the surface temperature above the water freezing point. We show how local and rapid destabilization of the cryosphere can be induced by large events (such as the Hellas Basin or Tharsis bulge formation) and lead to such releases. Our results show that the early Mars cryosphere had a sufficient CH4 storage capacity to have maintained H2‐rich transient atmospheres during a total time period up to several million years or tens of million years, having potentially contributed to the formation of valley networks during the Noachian/early Hesperian.  相似文献   

2.
Abstract– A model is presented in which the aqueous conditions needed to generate phyllosilicate minerals in the absence of carbonates found in the ancient Noachian crust are maintained by an early CO2‐rich atmosphere, that, together with iron (II) oxidation, would prevent carbonate formation at the surface. After cessation of the internal magnetic dynamo, a CO2‐rich primordial atmosphere was stripped by interactions with the solar wind and surface conditions evolved from humid to arid, with ground waters partially dissolving subsurface carbonate and sulfide minerals to produce acid‐sulfate evaporitic deposits in areas with upwelling ground water. In a subsequent geochemical state (Late Noachian to Hesperian), surface and subsurface acidic solutions were neutralized in the subsurface through interaction with basaltic crust, allowing the precipitation of secondary carbonates. This model suggests that, in the early Noachian, the surface waters of Mars maintained acidity because of a drop in temperature. This would have favored increased dissolution of CO2 and a reduction in atmospheric pressure. In this scenario, physicochemical conditions precluded the formation of surface carbonates, but induced the precipitation of carbonates in the subsurface.  相似文献   

3.
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   

4.
Volcanism has been a major process during most of the geologic history of Mars. Based on data collected from terrestrial basaltic eruptions, we assume that the volatile content of martian lavas was typically ∼0.5 wt.% water, ∼0.7 wt.% carbon dioxide, ∼0.14 wt.% sulfur dioxide, and contained several other important volatile constituents. From the geologic record of volcanism on Mars we find that during the late Noachian and through the Amazonian volcanic degassing contributed ∼0.8 bar to the martian atmosphere. Because most of the outgassing consisted of greenhouse gases (i.e., CO2 and SO2) warmer surface temperatures resulting from volcanic eruptions may have been possible. Our estimates suggest that ∼1.1 × 1021 g (∼8 ± 1 m m−2) of juvenile water were released by volcanism; slightly more than half the amount contained in the north polar cap and atmosphere. Estimates for released CO2 (1.6 × 1021 g) suggests that a large reservoir of carbon dioxide is adsorbed in the martian regolith or alternatively ∼300 cm cm−2 of carbonates may have formed, although these materials would not occur readily in the presence of excess SO2. Up to ∼120 cm cm−2 (2.2 × 1020 g) of acid rain (H2SO4) may have precipitated onto the martian surface as the result of SO2 degassing. The hydrogen flux resulting from volcanic outgassing may help explain the martian atmospheric D/H ratio. The amount of outgassed nitrogen (∼1.3 mbar) may also be capable of explaining the martian atmospheric 15N/14N ratio. Minor gas constituents (HF, HCl, and H2S) could have formed hydroxyl salts on the surface resulting in the physical weathering of geologic materials. The amount of hydrogen fluoride emitted (1.82 × 1018 g) could be capable of dissolving a global layer of quartz sand ∼5 mm thick, possibly explaining why this mineral has not been positively identified in spectral observations. The estimates of volcanic outgassing presented here will be useful in understanding how the martian atmosphere evolved over time.  相似文献   

5.
We review the mineralogy of the surface of Mars, using data from various sources, including in situ characterisations performed by landers, remote observations from orbit, and studies of the SNC meteorites. We also discuss the possible alteration processes and the factor controlling them, and try to relate the mineralogical observations to the chemical evolution of the surface materials on Mars in order to identify the dominant process(es). Then we try to describe a possible chemical and mineralogical evolution of the surface materials, resulting from weathering driven by the abundance and activity of water. Even if weathering is the dominant process responsible for the surface evolution, all observations suggest that it is strongly affected locally in time and space by various other processes including hydrothermalism, volcanism, evaporites, meteoritic impacts and aeolian erosion. Nevertheless, the observed phases on the surface of Mars globally depend on the evolution of the weathering conditions. This hypothesis, if confirmed, could give a new view of the evolution of the martian surface, roughly in three steps. The first would correspond to clay-type weathering process in the Noachian, under a probable thick H2O/CO2-rich atmosphere. Then, during the Hesperian when water became scarcer and its activity sporadic, linked to volcanic activity, sulfate-type acidic weathering process would have been predominant. The third period would be like today, a very slow weathering by strongly oxidising agents (H2O2, O2) in cold and dry conditions, through solid-gas or solid-films of water resulting frost-thaw and/or acid fog. This would favour poorly crystalline phases, mainly iron (oxy) hydroxides. But in this scenario many questions remain about the transition between these processes, and about the factors affecting the evolution of the weathering process.  相似文献   

6.
Abstract— Martian meteorites (MMs) have been launched from an estimated 5–9 sites on Mars within the last 20 Myr. Some 80–89% of these launch sites sampled igneous rock formations from only the last 29% of Martian time. We hypothesize that this imbalance arises not merely from poor statistics, but because the launch processes are dominated by two main phenomena: first, much of the older Martian surface is inefficient in launching rocks during impacts, and second, the volumetrically enormous reservoir of original cumulate crust enhances launch probability for 4.5 Gyr old rocks. There are four lines of evidence for the first point, not all of equal strength. First, impact theory implies that MM launch is favored by surface exposures of near‐surface coherent rock (≤102 m deep), whereas Noachian surfaces generally should have ≥102 m of loose or weakly cemented regolith with high ice content, reducing efficiency of rock launch. Second, similarly, both Mars Exploration Rovers found sedimentary strata, 1–2 orders of magnitude weaker than Martian igneous rocks, favoring low launch efficiency among some fluvial‐derived Hesperian and Noachian rocks. Even if launched, such rocks may be unrecognized as meteorites on Earth. Third, statistics of MM formation age versus cosmic‐ray exposure (CRE) age weakly suggest that older surfaces may need larger, deeper craters to launch rocks. Fourth, in direct confirmation, one of us (N. G. B.) has found that older surfaces need larger craters to produce secondary impact crater fields (cf. Barlow and Block 2004). In a survey of 200 craters, the smallest Noachian, Hesperian, and Amazonian craters with prominent fields of secondaries have diameters of ?45 km, ?19 km, and ?10 km, respectively. Because 40% of Mars is Noachian, and 74% is either Noachian or Hesperian, the subsurface geologic characteristics of the older areas probably affect statistics of recognized MMs and production rates of secondary crater populations, and the MM and secondary crater statistics may give us clues to those properties.  相似文献   

7.
In this paper, we use a statistical thermodynamic approach to quantify the efficiency with which clathrates on the surface of Titan trap noble gases. We consider different values of the Ar, Kr, Xe, CH4, C2H6 and N2 abundances in the gas phase that may be representative of Titan's early atmosphere. We discuss the effect of the various parameters that are chosen to represent the interactions between the guest species and the ice cage in our calculations. We also discuss the results of varying the size of the clathrate cages. We show that the trapping efficiency of clathrates is high enough to significantly decrease the atmospheric concentrations of Xe and, to a lesser extent, of Kr, irrespective of the initial gas phase composition, provided that these clathrates are abundant enough on the surface of Titan. In contrast, we find that Ar is poorly trapped in clathrates and, as a consequence, that the atmospheric abundance of argon should remain almost constant. We conclude that the mechanism of trapping noble gases via clathration can explain the deficiency in primordial Xe and Kr observed in Titan's atmosphere by Huygens, but that this mechanism is not sufficient to explain the deficiency in Ar.  相似文献   

8.
Calculations of the trapping of heavy noble gases within multiple guest clathrates under Mars-like conditions show that a substantial fraction of the martian Xe, perhaps even the vast majority, could be in clathrates. In addition, the Xe/Kr ratio in the clathrates would probably be much higher than in the atmosphere, so the formation or dissociation of a relatively small amount of clathrate could measurably change the atmospheric ratio. Relatively crude (factor of 2) measurements of the seasonal variability in that ratio by in situ spacecraft would be sensitive to ∼10% of the seasonal atmospheric CO2 variability being a result of clathrates, rather than pure CO2 frost. In addition, sequestration of Xe in clathrates remains a viable mechanism for explaining the variable Xe/Kr ratios seen in different suites of martian meteorites.  相似文献   

9.
《Planetary and Space Science》1999,47(3-4):411-431
We have constructed the complex geologic history of the Thaumasia region of Mars on the basis of detailed geologic mapping and relative-age dating of rock units and structure. The Thaumasia plateau dominates the region and consists of high lava plains partly surrounded by rugged highlands, mostly of Noachian and Hesperian age. Long-lived faulting centered near Syria Planum and at lesser sites produced radiating narrow grabens during the Noachian through Early Amazonian and concentric wrinkle ridges during the Late Noachian and Early Hesperian. Fault activity peaked during the Noachian and waned substantially during Late Hesperian and Amazonian time. Volcanism on the Thaumasia plateau was particularly active in comparison with other martian cratered highlands, resulting in fourteen volcanoes and numerous outcrops of smooth, ridged, and lobate plains materials. A particularly extensive set of overlapping lava-flow units was emplaced sequentially from Thaumasia Planum to Syria Planum, spanning from the Late Noachian to the Late Hesperian; lobate flows succeeded smooth flow at the beginning of the Late Hesperian. Deep crustal intrusion and a thickened, buoyant crust may have caused the uplift of the plateau during the Noachian and Early Hesperian, resulting in outward-verging fold-and-thrust plateau margins. This structural style appears similar to that of the young ranges of the Rocky Mountains in the western U.S. Within the plateau, several sites of volcanotectonic activity and valley erosion may be underlain by large and perhaps long-lived magmatic intrusions. One such site occurs at the headland of Warrego Valles. Here, at least two episodes of valley dissection from the Noachian to Early Hesperian occurred during the formation of two nearby rift systems. The site also is a locus of intersection for regional narrow grabens during the Late Noachian and Early Hesperian. However, at the site, such faults diverge or terminate, which suggests that a resistant body of rock occurs there. The overall volcanotectonic history at Thaumasia fits into a model for Tharsis as a whole in which long-lived Syria Planum-centered activity is ringed by a few significant, shorter-lived centers of activity like the Thaumasia plateau. Valley formation, like tectonism in the region, peaked during the Noachian and declined substantially during the Hesperian and Amazonian. Temporal and spatial associations of single erosional valleys and valley networks with volcanoes, rift systems, and large impact craters suggest that the majority of valleys formed by hydrothermal, deformational, and seismic-induced processes. The origin of scattered, mainly Noachian valleys is more conjectural; possible explanations include local precipitation, seismic disturbance of aquifers, or unrecognized intrusions.  相似文献   

10.
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.  相似文献   

11.
Recent papers attributing the observed microwave opacity of the middle atmosphere of Venus to gaseous sulfur dioxide (SO2) and other cloud-related gases have motivated laboratory measurements of their microwave absorbing properties under simulated conditions for this region. In the pressure range from 1 to 5 atmospheres and in the temperature range from 297 to 355°K, the absorption of SO2 in a carbon dioxide (CO2) atmosphere, at 2.257 and 8.342 GHz, has been found to be approximately 50% larger than that calculated from Van Vleck-Weisskopf theory. The measured absorption is about 25 × 106 q?2p1.20 T?3.1 (dB km?1), where q is the sulfur dioxide number mixing ratio, ? is frequency in gigahertz, p is pressure in atmospheres, and T is temperature in degrees Kelvin. This represents the best-fit expression to the observed pressure dependence, while theoretical values of frequency and temperature dependence are accepted as being consistent with the measurements. Another cloud-related gas, sulfur trioxide (SO3), was also tested in a CO2 atmosphere and found to be relatively transparent. These results reduce the amount of SO2 in the Venus middle atmosphere required to explain the opacity measured by radio occulatation, but this amount still exceeds the abundance measured in situ by atmospheric probes, suggesting that there must be another important source of opacity. Preliminary measurements of the 13-cm absorptivity of gaseous sulfuric acid (H2SO4) show it to be a strong microwave absorber, and thus likely to be responsible for a significant and possibly major part of the observed opacity.  相似文献   

12.
We present an updated model for the photochemistry of Io's atmosphere and ionosphere and use this model to investigate the sensitivity of the chemical structure to vertical transport rates. SO2is assumed to be the dominant atmospheric gas, with minor molecular sodium species such as Na2S or Na2O released by sputtering or venting from the surface. Photochemical products include SO, O2, S, O, Na, NaO, NaS, and Na2. We consider both “thick” and “thin” SO2atmospheres that encompass the range allowed by recent HST and millimeter-wave observations, and evaluate the possibility that O2and/or SO may be significant minor dayside constituents and therefore likely dominant nightside gases. The fast reaction between S and O2limits the column abundance of O2to ∼104less than that calculated by Kumar (J. Geophys. Res.87, 1677–1684, 1982; 89(A9), 7399–7406, 1984) for a pure sulfur/oxygen atmosphere. If a significant source of NaO2or Na2O were supplied by the surface and mixed rapidly upward, then oxygen liberated in the chemical reactions which also liberate free Na would provide an additional source of O2. Fast eddy mixing will enhance the transport of molecular sodium species to the exobase, in addition to increasing the vertical transport rate of ions. Ions produced in the atmosphere will be accelerated by the reduced corotation electric field penetrating the atmosphere. These ions experience collisions with the neutral gas, leading to enhanced vertical ion diffusion. The dominant ion, Na+, is lost primarily by charge exchange with Na2O and/or Na2S in the lower atmosphere and by diffusion through the ionopause in the upper atmosphere. The atmospheric column abundance of SO, O2, and the upper atmosphere escape rates of Na, S, O, and molecular sodium species are all strong functions of the eddy mixing rate. Most atmospheric escape, including that of molecular sodium species, probably occurs from the low density “background” SO2atmosphere, while a localized high density “volcanic” SO2atmosphere can yield an ionosphere consistent with that detected by the Pioneer 10 spacecraft.  相似文献   

13.
Clouds and hazes composed of sulfuric acid are observed to exist or postulated to have once existed on each of the terrestrial planets with atmospheres in our solar system. Venus today maintains a global cover of clouds composed of a sulfuric acid/water solution that extends in altitude from roughly 50 km to roughly 80 km. Terrestrial polar stratospheric clouds (PSCs) form on stratospheric sulfuric acid aerosols, and both PSCs and stratospheric aerosols play a critical role in the formation of the ozone hole. Stratospheric aerosols can modify the climate when they are enhanced following volcanic eruptions, and are a current focus for geoengineering studies. Rain is made more acidic by sulfuric acid originating from sulfur dioxide generated by industry on Earth. Analysis of the sulfur content of Martian rocks has led to the hypothesis that an early Martian atmosphere, rich in SO2 and H2O, could support a sulfur-infused hydrological cycle. Here we consider the plausibility of frozen sulfuric acid in the upper clouds of Venus, which could lead to lightning generation, with implications for observations by the European Space Agency's Venus Express and the Japan Aerospace Exploration Agency's Venus Climate Orbiter (also known as Akatsuki). We also present simulations of a sulfur-rich early Martian atmosphere. We find that about 40 cm/yr of precipitation having a pH of about 2.0 could fall in an early Martian atmosphere, assuming a surface temperature of 273 K, and SO2 generation rates consistent with the formation of Tharsis. This modeled acid rain is a powerful sink for SO2, quickly removing it and preventing it from having a significant greenhouse effect.  相似文献   

14.
O. Gomis  G. Strazzulla 《Icarus》2008,194(1):146-152
In this paper we present the results of new experiments of ion irradiation of water ice deposited on top of a solid sulfurous residue to study the potential formation of SO2 at the interface ice/refractory material and discuss the possibility that this mechanism accounts for the sulfur dioxide ice detected on the surfaces of the Galilean satellites. In situ infrared spectroscopy was the used experimental technique. We have irradiated a thin film of H2O frost on a sulfurous layer with 200 keV of He+ at 80 K. The used sulfurous residue was obtained by irradiation of frozen SO2 at 16 K and it is used as a template of sulfur bearing solid materials. We have not found evidences of the efficient formation of SO2 after irradiation of H2O ice on top of the sulfurous residue. An upper limit to the production yield of SO2, of interface area for each 100 eV of energy absorbed in 1 cm3 of ice-covered residue, has been estimated. These results have relevance in the context of the surfaces of the icy Galilean satellites in which SO2 was detected. Our results show that radiolysis of mixtures of water ice and refractory sulfurous materials is not the primary formation mechanism responsible for the SO2 present on the surfaces of the Galilean satellites.  相似文献   

15.
Chemical kinetic model for the lower atmosphere of Venus   总被引：1，自引：0，他引：1  
A self-consistent chemical kinetic model of the Venus atmosphere at 0-47 km has been calculated for the first time. The model involves 82 reactions of 26 species. Chemical processes in the atmosphere below the clouds are initiated by photochemical products from the middle atmosphere (H2SO4, CO, Sx), thermochemistry in the lowest 10 km, and photolysis of S3. The sulfur bonds in OCS and Sx are weaker than the bonds of other elements in the basic atmospheric species on Venus; therefore the chemistry is mostly sulfur-driven. Sulfur chemistry activates some H and Cl atoms and radicals, though their effect on the chemical composition is weak. The lack of kinetic data for many reactions presents a problem that has been solved using some similar reactions and thermodynamic calculations of inverse processes. Column rates of some reactions in the lower atmosphere exceed the highest rates in the middle atmosphere by two orders of magnitude. However, many reactions are balanced by the inverse processes, and their net rates are comparable to those in the middle atmosphere. The calculated profile of CO is in excellent agreement with the Pioneer Venus and Venera 12 gas chromatographic measurements and slightly above the values from the nightside spectroscopy at 2.3 μm. The OCS profile also agrees with the nightside spectroscopy which is the only source of data for this species. The abundance and vertical profile of gaseous H2SO4 are similar to those observed by the Mariner 10 and Magellan radio occultations and ground-based microwave telescopes. While the calculated mean S3 abundance agrees with the Venera 11-14 observations, a steep decrease in S3 from the surface to 20 km is not expected from the observations. The ClSO2 and SO2Cl2 mixing ratios are ∼10−11 in the lowest scale height. The existing concept of the atmospheric sulfur cycles is incompatible with the observations of the OCS profile. A scheme suggested in the current work involves the basic photochemical cycle, that transforms CO2 and SO2 into SO3, CO, and Sx, and a minor photochemical cycle which forms CO and Sx from OCS. The net effect of thermochemistry in the lowest 10 km is formation of OCS from CO and Sx. Chemistry at 30-40 km removes the downward flux of SO3 and the upward flux of OCS and increases the downward fluxes of CO and Sx. The geological cycle of sulfur remains unchanged.  相似文献   

16.
The large backscattering cross section of the particles composing the upper clouds on Venus suggests that a small quantity of high refractive index material is present in the clouds. We propose that this material is elemental sulfur and that sulfur also accounts for the absorption of uv-visible radiation at wavelengths outside of the SO2 absorption bands. A physical-chemical model of the clouds shows that sulfur, with a mass comparable to that of the observed Mode 1 particles, can be produced in oxygen-poor regions of the upper clouds and in rising air columns. Sulfur production from SO2 can be rapid, which explains the observed correlation between SO2 and the uv absorber. The sulfur is properly located to be the uv absorber uv absorber since its calculated concentration rapidly increases with depth in the upper clouds, but it is largely absent in the middle and lower clouds. Sulfur nucleation provides a means of generating the observed bimodal particle size distribution in the upper clouds. Chemical modeling shows that the sulfur vapor is rich in short-chain allotropes such as S3 and S4. These allotropes have absorption bands centered near 4000 and 5300 Å, respectively. We suggest that the sulfur particles on Venus are largely composed of S8, but also contain a few percent of S3 and S4. Such particles could account for the wavelength dependence of the albedo of Venus and for the solar energy deposition profile in the clouds. These allotropes are metastable and relax to S8 over periods of hours to days, providing a simple explanation for the relatively short lifetime of the uv absorber.  相似文献   

17.
Water is not currently stable in liquid form on the martian surface due to the present mean atmospheric pressure of ～7 mbar and mean global temperature of ～220 K. However, geomorphic features and hydrated mineral assemblages suggest that Mars’ climate was once warmer and liquid water flowed on the surface. These observations may indicate a substantially more massive atmosphere in the past, but there have been few observational constraints on paleoatmospheric pressures. Here we show how the 40Ar/36Ar ratios of trapped gases within martian meteorite ALH 84001 constrain paleoatmospheric pressure on Mars during the Noachian era [～4.56–3.8 billion years (Ga)]. Our model indicates that atmospheric pressures did not exceed ～1.5 bar during the first 400 million years (Ma) of the Noachian era, and were <400 mbar by 4.16 Ga. Such pressures of CO2 are only sufficient to stabilize liquid water on Mars’ surface at low latitudes during seasonally warm periods. Other greenhouse gases like SO2 and water vapor may have played an important role in intermittently stabilizing liquid water at higher latitudes following major volcanic eruptions or impact events.  相似文献   

18.
The composition of the atmosphere is regulated by biological activity on a variety of time scales. Global biogeochemical cycles of nitrogen, carbon and sulfur are discussed with an emphasis on N2O, NO, CO2, CH4 and SO2. It is argued that Man is a major influence on the budget of these gases. His influence is attributed primarily to use of fossil fuels, to various aspects of agriculture and to the disposal of human and animal waste.  相似文献   

19.
The polar condensation/sublimation of CO2, that involve about one fourth of the atmosphere mass, is the major Martian climatic cycle. Early observations in visible and thermal infrared have shown that the sublimation of the Seasonal South Polar Cap (SSPC) is not symmetric around the geographic South Pole.Here we use observations by OMEGA/Mars Express in the near-infrared to detect unambiguously the presence of CO2 at the surface, and to estimate albedo. Second, we estimate the sublimation of CO2 released in the atmosphere and show that there is a two-step process. From Ls=180° to 220°, the sublimation is nearly symmetric with a slight advantage for the cryptic region. After Ls=220° the anti-cryptic region sublimation is stronger. Those two phases are not balanced such that there is 22% ± 9 more mass the anti-cryptic region, arguing for more snow precipitation. We compare those results with the MOLA height measurements. Finally we discuss implications for the Martian atmosphere about general circulation and gas tracers, e.g. Ar.  相似文献   

20.
Several substances besides water ice have been detected on the surface of Europa by spectroscopic sensors, including CO2, SO2, and H2S. These substances might occur as pure crystalline ices, as vitreous mixtures, or as clathrate hydrate phases, depending on the system conditions and the history of the material. Clathrate hydrates are crystalline compounds in which an expanded water ice lattice forms cages that contain gas molecules. The molecular gases that may constitute Europan clathrate hydrates may have two possible ultimate origins: they might be primordial condensates from the interstellar medium, solar nebula, or jovian subnebula, or they might be secondary products generated as a consequence of the geological evolution and complex chemical processing of the satellite. Primordial ices and volatile-bearing compounds would be difficult to preserve in pristine form in Europa without further processing because of its active geological history. But dissociated volatiles derived from differentiation of a chondritic rock or cometary precursor may have produced secondary clathrates that may be present now. We have evaluated the current stability of several types of clathrate hydrates in the crust and the ocean of Europa. The depth at which the clathrates of SO2, CO2, H2S, and CH4 are stable have been obtained using both the temperatures observed in the surface [Spencer, J.R., Tamppari, L.K., Martin, T.Z., Travis, L.D., 1999. Temperatures on Europa from Galileo photopolarimeter-radiometer: Nighttime thermal anomalies. Science 284, 1514-1516] and thermal models for the crust. In addition, their densities have been calculated in order to determine their buoyancy in the ocean, obtaining different results depending upon the salinity of the ocean and type of clathrate. For instance, assuming a eutectic composition of the system MgSO4H2O for the ocean, CO2, H2S, and CH4 clathrates would float but SO2 clathrate would sink to the seafloor; an ocean of much lower salinity would allow all these clathrates to sink, except that CH4 clathrate would still float. Many geological processes may be driven or affected by the formation, presence, and destruction of clathrates in Europa such as explosive cryomagmatic activity [Stevenson, D.J., 1982. Volcanism and igneous processes in small icy satellites. Nature 298, 142-144], partial differentiation of the crust driven by its clathration, or the local retention of heat within or beneath clathrate-rich layers because of the low thermal conductivity of clathrate hydrates [Ross, R.G., Kargel, J.S., 1998. Thermal conductivity of Solar System ices, with special reference to martian polar caps. In: Schmitt, B., De Berg, C., Festou, M. (Eds.), Solar System Ices. Kluwer Academic, Dordrecht, pp. 33-62]. On the surface, destabilization of these minerals and compounds, triggered by fracture decompression or heating could result in formation of chaotic terrain morphologies, a mechanism that also has been proposed for some martian chaotic terrains [Tanaka, K.L., Kargel, J.S., MacKinnon, D.J., Hare, T.M., Hoffman, N., 2002. Catastrophic erosion of Hellas basin rim on Mars induced by magmatic intrusion into volatile-rich rocks. Geophys. Res. Lett. 29 (8); Kargel, J.S., Prieto-Ballesteros, O., Tanaka K.L., 2003. Is clathrate hydrate dissociation responsible for chaotic terrains on Earth, Mars, Europa, and Triton? Geophys. Res. 5. Abstract 14252]. Models of the evolution of the ice shell of Europa might take into account the presence of clathrate hydrates because if gases are vented from the silicate interior to the water ocean, they first would dissolve in the ocean and then, if the gas concentrations are sufficient, may crystallize. If any methane releases occur in Europa by hydrothermal or biological activity, they also might form clathrates. Then, from both geological and astrobiological perspectives, future missions to Europa should carry instrumentation capable of clathrate hydrate detection.  相似文献   

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