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1.
The presence of water-bearing minerals on Mars has long been discussed, but little or no data exist showing that minerals such as smectites and zeolites may be present on the surface in a hydrated state (i.e., that they could contain H2O molecules in their interlayer or extra-framework sites, respectively). We have analyzed experimental thermodynamic and X-ray powder diffraction data for smectite and the most common terrestrial zeolite, clinoptilolite, to evaluate the state of hydration of these minerals under martian surface conditions. Thermodynamic data for clinoptilolite show that water molecules in its extra-framework sites are held very strongly, with enthalpies of dehydration for Ca-clinoptilolite up to three times greater than that for liquid water. Using these data, we calculated the Gibbs free energy of hydration of clinoptilolite and smectite as a function of temperature and pressure. The calculations demonstrate that these minerals would indeed be hydrated under the very low-P (H2O) conditions existing on Mars, a reflection of their high affinities for H2O. These calculations assuming the partial pressure of H2O and the temperature range expected on Mars suggest that, if present on the surface, zeolites and Ca-smectites could also play a role in affecting the diurnal variations in martian atmospheric H2O because their calculated water contents vary considerably over daily martian temperature ranges. The open crystal structure of clinoptilolite and existing hydration and kinetic data suggest that hydration/dehydration are not kinetically limited. Based on these calculations, it is possible that hydrated zeolites and clay minerals may explain some of the recent observations of significant amounts of hydrogen not attributable to water ice at martian mid-latitudes.  相似文献   

2.
Spores of Bacillus subtilis were used as a model system to study the impact of the two major DNA double-strand break (DSB) repair mechanisms [homologous recombination (HR) and non-homologous end-joining (NHEJ)] on the survivability of air-dried mono- and multilayers of bacterial spores under a simulated martian environment; i.e., an environment with low temperature (−10 °C), pure CO2 atmosphere (99.99% CO2), 200-1100 nm UV-VIS-NIR radiation, and 0.69 kPa pressure. Spores in multilayers exhibited low inactivation rates compared to monolayers, mainly due to shadowing effects of overlying spores. Simulated martian UV irradiation reduced dramatically spore viability, whereas when shielded from martian UV radiation, spores deficient in NHEJ- and HR-mediated DNA repair were significantly more sensitive to simulated martian environmental conditions than were wild-type spores. In addition, NHEJ-deficient spores were consistently more sensitive than HR-deficient spores to simulated Mars environmental conditions, suggesting that DSBs were an important type of DNA damage. The results indicated that both HR and NHEJ provide an efficient set of DNA repair pathways ensuring spore survival after exposure to simulated martian environmental conditions.  相似文献   

3.
The interval from Ls = 330° in Mars Year (MY) 26 until Ls = 84° in MY 27 has been used to compare and validate measurements from the Mars Global Surveyor Thermal Emission Spectrometer (TES) and the Mars Express Planetary Fourier Spectrometer (PFS). We studied differences between atmospheric temperatures observed by the two instruments. The best agreement between atmospheric temperatures was found at 50 Pa between 40°S and 40°N latitude, where differences were within ±5 K. For other atmospheric levels, differences as large as ∼25 K were observed between the two instruments at some locations. The largest temperature differences occurred mainly over the Hellas Planitia, Argyre Planitia, Tharsis and Valles Marineris regions.On this basis we report on the variability of the martian atmosphere during the 5.5 martian years of Mars climatology obtained by combining the two data sets from TES and PFS. Atmospheric temperatures at 50 Pa responded to the global-scale dust storms of MY 25 and in MY 28 raising temperatures from ∼220 K to ∼250 K during the daytime. An atmospheric temperature of ∼140 K at 50 Pa was observed poleward of 70°N during northern winter and poleward of 60°S during southern winter each year in both the PFS and TES results. Water vapor observed by the two spectrometers showed consistent seasonal and latitudinal variations.  相似文献   

4.
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.  相似文献   

5.
Encouraged by recent results of the Mars Odyssey spacecraft mission and the OMEGA team (Mars Express) concerning water in equatorial latitudes between ±45° on Mars and the possible existence of hydrated minerals, we have investigated the water sorption properties of natural zeolites and clay minerals close to martian atmospheric surface conditions as well as the properties of Mg-sulfates and gypsum. To quantify the stability of hydrous minerals on the martian surface and their interaction with the martian atmosphere, the water adsorption and desorption properties of nontronite, montmorillonite, chabazite and clinoptilolite have been investigated using adsorption isotherms at low equilibrium water vapor pressures and temperatures, modeling of the adsorption equilibrium data, thermogravimetry (TG), differential scanning calorimetry (DSC), and proton magic angle spinning nuclear magnetic resonance measurements (1H MAS NMR). Mg-sulfate hydrates were also analyzed using TG/DSC methods to compare with clay mineral and zeolites. Our data show that these microporous minerals can remain hydrated under present martian atmospheric conditions and hold up to 2.5-25 wt% of water in their void volumes at a partial water vapor pressure of 0.001 mbar in a temperature range of 333-193 K. Results of the 1H MAS NMR measurements suggest that parts of the adsorbed water are liquid-like water and that the mobility of the adsorbed water might be of importance for adsorption-water-triggered chemistry and hypothetical exobiological activity on Mars.  相似文献   

6.
Steven W. Ruff 《Icarus》2004,168(1):131-143
Spectral features observed in Mars Global Surveyor Thermal Emission Spectrometer data (∼1670-220 cm−1) of martian surface dust provide clues to its mineralogy. An emissivity peak at ∼1630 cm−1 is consistent with the presence of an H2O-bearing mineral. This spectral feature can be mapped globally and shows a distribution related to the classical bright regions on Mars that are known to be dust covered. An important spectral feature at ∼830 cm−1 present in a newly derived average spectrum of surface dust likely is a transparency feature arising from the fine particulate nature of the dust. Its shape and location are consistent with plagioclase feldspars and also zeolites, which essentially are the hydrous form of feldspar. The generally favored visible/near-infrared spectral analog for martian dust, JSC Mars-1 altered tephra, does not display the ∼830 cm−1 feature. Zeolites commonly form from the interaction of low temperature aqueous fluids and volcanic glass in a variety of geologic settings. The combination of spectral features that are consistent with zeolites and the likelihood that Mars has (or had) geologic conditions necessary to produce them makes a strong case for recognizing zeolite minerals as likely components of the martian regolith.  相似文献   

7.
Using the Fourier Transform Spectrometer at the Canada-France-Hawaii Telescope, we observed a spectrum of Mars at the P-branch of the strongest CH4 band at 3.3 μm with resolving power of 180,000 for the apodized spectrum. Summing up the spectral intervals at the expected positions of the 15 strongest Doppler-shifted martian lines, we detected the absorption by martian methane at a 3.7 sigma level which is exactly centered in the summed spectrum. The observed CH4 mixing ratio is 10±3 ppb. Total photochemical loss of CH4 in the martian atmosphere is equal to , the CH4 lifetime is 340 years and methane should be uniformly mixed in the atmosphere. Heterogeneous loss of atmospheric methane is probably negligible, while the sink of CH4 during its diffusion through the regolith may be significant. There are no processes of CH4 formation in the atmosphere, so the photochemical loss must therefore be balanced by abiogenic and biogenic sources. Outgassing from Mars is weak, the latest volcanism is at least 10 million years old, and thermal emission imaging from the Mars Odyssey orbiter does not reveal any hot spots on Mars. Hydrothermal systems can hardly be warmer than the room temperature at which production of methane is very low in terrestrial waters. Therefore a significant production of hydrothermal and magmatic methane is not very likely on Mars. The calculated average production of CH4 by cometary impacts is 2% of the methane loss. Production of methane by meteorites and interplanetary dust does not exceed 4% of the methane loss. Methane cannot originate from an extinct biosphere, as in the case of “natural gas” on Earth, given the exceedingly low limits on organic matter set by the Viking landers and the dry recent history which has been extremely hostile to the macroscopic life needed to generate the gas. Therefore, methanogenesis by living subterranean organisms is a plausible explanation for this discovery. Our estimates of the biomass and its production using the measured CH4 abundance show that the martian biota may be extremely scarce and Mars may be generally sterile except for some oases.  相似文献   

8.
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   

9.
The origin and nature of the early atmosphere of Mars is still debated. The discovery of sulfate deposits on the surface, coupled with the evidence that there are not large abundances of carbonates detectable on Mars in the optically accessible part of the regolith, leaves open different paleoclimatic evolutionary pathways. Even if carbonates are responsible for the feature observed by TES and Mini-TES at 6.76 μm, alternative hypotheses suggest that it could be due to the presence of Hydrated Iron Sulfates (HIS). Carbonates can be discerned from HIS by investigating the spectral region in which a strong overtone carbonate band is present. The Planetary Fourier Spectrometer on board the Mars Express spacecraft has acquired several thousand martian spectra in the range 1.2-45 μm since January 2004, most of which show a weak absorption feature between 3.8 and 4 μm. A similar feature was observed previously from the Earth, but its origin could not be straightforwardly ascribed to surface materials, and specifically to carbonates. Here we show the surficial nature of this band that can be ascribed to carbonate mixed with the martian soil materials. The materials that best reproduce the detected feature are Mg-rich carbonates (huntite [CaMg3(CO3)4] and/or magnesite [MgCO3]). The presence of carbonates is demonstrated in both bright and dark martian regions. An evaluation of the likeliest abundance gives an upper limit of ∼10 wt%. The widespread distribution of carbonates supports scenarios that suggest carbonate formation occurred not by precipitation in a water-rich environment but by weathering processes.  相似文献   

10.
F. Altieri  L. Zasova  G. Bellucci  B. Gondet 《Icarus》2009,204(2):499-511
We present a method to derive the 2D maps of the O2 (a1Δg) airglow emission at 1.27 μm from the OMEGA/MEx nadir observations. The OMEGA imaging capabilities allow monitoring the 2D distribution, daily and seasonal variation of the O2 emission intensities with a detection limit of 4 MR. The highest values, of the order of ∼31 MR, are found on the south pole for 11 h < LT < 13 h, during the early spring (186° < Ls < 192°) of martian year (MY) 27, according to the Mars Year numbering scheme of Clancy et al. [Clancy, R.T., Wolff, M.J., Christensen, P.R., 2003. Mars aerosol studies with the MGS TES emission phase function observations: Optical depths, particle sizes, and ice cloud types versus latitude and solar longitude. J. Geophys. Res. 108. doi: 10.1029/2003JE002058]. In the polar regions the day-by-day variability, associated with polar vortex turbulences, is obtained of the order of 30-50% as predicted by the model [Lefévre, F., Lebonnois, S., Montmessin, F., Forget, F., 2004. Three-dimensional modeling of ozone on Mars. J. Geophys. Res. 109, E07004. doi: 10.1029/2004JE002268] and found by SPICAM [Perrier, S., Bertaux, J.-L., Lebonnois, S., Korablev, O., Fedorova, A., 2006. Global distribution of total ozone on Mars from SPICAM/MEX UV measurements. J. Geophys. Res. 111, E09S06. doi: 10.1029/2006JE002681]. In the considered set of data a maximum of the O2 emission is observed between 11 h and 15 h LT in the latitude range 70-85° during early spring on both hemispheres, while for the southern autumn-winter season a maximum is found between 50° and 60° in the southern hemisphere for MY28. Increase of intensity of the O2 emission observed from Ls 130° to 160° at southern high latitudes may be explained by increase of solar illumination conditions in the maps acquired during the considered period.Atmospheric waves crossing the terminator on the southern polar regions are observed for the first time during the MY28 early spring. The spatial scale of the waves ranges from 100 to 130 km, and the intensity fluctuations are of the order of 4MR.This study confirms the high potentiality of O2 (a1Δg) day glow as a passive tracer of the martian atmosphere dynamics at high latitudes.  相似文献   

11.
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.  相似文献   

12.
The Tyrrhena Terra region of Mars is studied with the imaging spectrometers OMEGA (Observatoire pour la Minéralogie, l’Eau, les Glaces et l’Activité) onboard Mars Express and CRISM (Compact Reconnaissance Infrared Spectrometer for Mars) onboard Mars Reconnaissance Orbiter, through the observation of tens of craters that impacted into this part of the martian highlands. The 175 detections of hydrated silicates are reported, mainly associated with ejecta blankets, crater walls and rims, and central up-lifts. Sizes of craters where hydrated silicates are detected are highly variable, diameters range from less than 1 km to 42 km. We report the presence of zeolites and phyllosilicates like prehnite, Mg-chlorite, Mg-rich smectites and mixed-layer chlorites–smectites and chlorite–vermiculite from comparison of hyperspectral infrared observations with laboratory spectra. These minerals are associated with fresh craters post-dating any aqueous activity. They likely represent ancient hydrated terrains excavated by the crater-forming impacts, and hence reveal the composition of the altered Noachian crust, although crater-related hydrothermal activity may have played a minor role for the largest craters (>20 km in diameter). Most detected minerals formed over relatively high temperatures (100–300 °C), likely due to aqueous alteration of the Noachian crust by regional low grade metamorphism from the Noachian thermal gradient and/or by extended hydrothermal systems associated with Noachian volcanism and ancient large impact craters. This is in contrast with some other phyllosilicate-bearing regions like Mawrth Vallis where smectites, kaolinites and hydrated silica were mainly identified, pointing to a predominance of surface/shallow sub-surface alteration; and where excavation by impacts played only a minor role. Smooth plains containing hydrated silicates are observed at the boundary between the Noachian altered crust, dissected by fluvial valleys, and the Hesperian unaltered volcanic plains. These plains may correspond to alluvial deposition of eroded material. The highlands of Tyrrhena Terra are therefore particularly well suited for investigating the diversity of hydrated minerals in ancient martian terrains.  相似文献   

13.
There have been several reports of methane on Mars at the 10-60 ppbv level. Most suggest that methane is both seasonally and latitudinally variable. Here we review why variable methane on Mars is physically and chemically implausible, and then we critically review the published reports. There is no known mechanism for destroying methane chemically on Mars. But if there is one, methane oxidation would deplete the O2 in Mars’s atmosphere in less than 10,000 years unless balanced by an equally large unknown source of oxidizing power. Physical sequestration does not raise these questions, but adsorption in the regolith or condensation in clathrates ignore competition for adsorption sites or are inconsistent with clathrate stability, respectively. Furthermore, any mechanism that relies on methane’s van der Waals’ attraction is inconsistent with the continued presence of Xe in the atmosphere at the 60 ppbv level. We then use the HITRAN database and transmission calculations to identify and characterize the absorption lines that would be present on Earth or Mars at the wavelengths of the published observations. These reveal strong competing telluric absorption that is most problematic at just those wavelengths where methane’s signature seems most clearly seen from Earth. The competing telluric lines must be removed with models. The best case for martian methane was made for the 12CH4ν3 R0 and R1 lines seen in blueshift when Mars was approaching Earth in early 2003 (Mumma, M.J., Villanueva, G.L., Novak, R.E., Hewagama, T., Bonev, B.P., DiSanti, M.A., Mandell, A.M., Smith, M.D. [2009]. Science 323, 1041-1045). For these the Doppler shift moves the two martian lines into near coincidence with telluric 13CH4ν3 R1 and R2 lines that are 10-50× stronger than the inferred martian lines. By contrast, the 12CH4ν3 R0 and R1 lines when observed in redshift do not contend with telluric 13CH4. For these lines, Mumma et al.’s observations and analyses are consistent with an upper limit on the order of 3 ppbv.  相似文献   

14.
L.J. Preston  G.K. Benedix 《Icarus》2008,198(2):331-350
Surface features observed on Mars and evidence from martian meteorites both suggest that hydrothermal systems have operated in the crust of the planet. Hydrothermal systems are a potential habitat for living organisms and identifying these on Mars is, therefore, important in the search for life beyond the Earth. One of the surface expressions of hydrothermal systems on Earth are silica sinters, deposited during the cooling of hydrothermal solutions. In this paper we present analyses of the mineralogy, textures, chemistry and organic chemistry of silica sinters from two very different geothermal provinces, Waiotapu, New Zealand and Haukadalur, Iceland, in order to determine common features by which silica sinters can be identified. Infrared reflectance spectroscopy was utilised in combination with textural studies to evaluate the mineralogy of sinter deposits in terms of the abundances of different polymorphs of SiO2. Concentrations of organic molecules, principally lipids, within regions of the sinters in which there is textural evidence for micro-organisms were identified in the infrared spectral data and their presence was confirmed using gas chromatography mass spectroscopy. The results of this study indicate that reflectance spectra in the wavelength region from 2.5 to 14 μm, when calibrated against natural terrestrial analogues, can be used to identify silica sinters, as well as the possible presence of recent microbial communities on Mars.  相似文献   

15.
High-resolution infrared imaging spectroscopy of Mars has been achieved at the NASA Infrared Telescope Facility (IRTF) on June 19-21, 2003, using the Texas Echelon Cross Echelle Spectrograph (TEXES). The areocentric longitude was 206°. Following the detection and mapping of hydrogen peroxide H2O2 [Encrenaz et al., 2004. Icarus 170, 424-429], we have derived, using the same data set, a map of the water vapor abundance. The results appear in good overall agreement with the TES results and with the predictions of the Global Circulation Model (GCM) developed at the Laboratory of Dynamical Meteorology (LMD), with a maximum abundance of water vapor of 3±1.5×10−4(17±9 pr-μm). We have searched for CH4 over the martian disk, but were unable to detect it. Our upper limits are consistent with earlier reports on the methane abundance on Mars. Finally, we have obtained new measurements of CO2 isotopic ratios in Mars. As compared to the terrestrial values, these values are: (18O/17O)[M/E] = 1.03 ± 0.09; (13C/12C)[M/E] = 1.00 ± 0.11. In conclusion, in contrast with the analysis of Krasnopolsky et al. [1996. Icarus 124, 553-568], we conclude that the derived martian isotopic ratios do not show evidence for a departure from their terrestrial values.  相似文献   

16.
NASA’s Phoenix lander identified perchlorate and carbonate salts on Mars. Perchlorates are rare on Earth, and carbonates have largely been ignored on Mars following the discovery by NASA’s Mars Exploration Rovers of acidic precipitated minerals such as jarosite. In light of the Phoenix results, we updated the aqueous thermodynamic model FREZCHEM to include perchlorate chemistry. FREZCHEM models the Na-K-Mg-Ca-Fe(II)-Fe(III)-Al-H-Cl-Br-SO4-NO3-OH-HCO3-CO3-CO2-O2-CH4-Si-H2O system, with 95 solid phases. We added six perchlorate salts: NaClO4·H2O, NaClO4·2H2O, KClO4, Mg(ClO4)2·6H2O, Mg(ClO4)2·8H2O, and Ca(ClO4)2·6H2O. Modeled eutectic temperatures for Na, Mg, and Ca perchlorates ranged from 199 K (−74 °C) to 239 K (−34 °C) in agreement with experimental data.We applied FREZCHEM to the average solution chemistry measured by the Wet Chemistry Laboratory (WCL) experiment at the Phoenix site when soil was added to water. FREZCHEM was used to estimate and alkalinity concentrations that were missing from the WCL data. The amount of is low compared to estimates from elemental abundance made by other studies on Mars. In the charge-balanced solution, the dominant cations were Mg2+ and Na+ and the dominant anions were , and alkalinity. The abundance of calcite measured at the Phoenix site has been used to infer that the soil may have been subject to liquid water in the past, albeit not necessarily locally; so we used FREZCHEM to evaporate (at 280.65 K) and freeze (from 280.65 to 213.15 K) the WCL-measured solution to provide insight into salts that may have been in the soil. Salts that precipitated under both evaporation and freezing were calcite, hydromagnesite, gypsum, KClO4, and Mg(ClO4)2·8H2O. Epsomite (MgSO4·7H2O) and NaClO4·H2O were favored by evaporation at temperatures >0 °C, while meridianite (MgSO4·11H2O), MgCl2·12H2O, and NaClO4·2H2O were favored at subzero temperatures. Incongruent melting of such highly hydrated salts could be responsible for vug formation elsewhere on Mars.All K+ precipitated as insoluble KClO4 during both evaporation and freezing simulations, accounting for 15.8% of the total perchlorates. During evaporation, 35.8% of perchlorates precipitated with Na+ and 48.4% with Mg2+. During freezing, 58.4% precipitated with Na+ and 24.8% with Mg2+. Given its low eutectic temperature, the existence of Mg(ClO4)2 in either case allows for the possibility of liquid brines on Mars today. FREZCHEM also showed that Ca(ClO4)2 would likely not have precipitated at the Phoenix landing site due to the strong competing sinks for Ca as calcite and gypsum. Overall, these results help constrain the salt mineralogy of the soil. Differences between evaporites and cryogenites suggest ways to discriminate between evaporation and freezing during salt formation. Future efforts, such as sample return or in situ X-ray diffraction, may make such a determination possible.  相似文献   

17.
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18.
The role of water ice clouds in the martian water cycle and climate depends on cloud properties such as particle size and number distribution. These properties, in turn, depend on heterogeneous nucleation parameters which are poorly understood. Here we report laboratory experiments performed under martian temperature and water partial pressure conditions (158–185 K, 9 × 10−7–1 × 10−4 Torr H2O) to determine the critical saturation ratio for ice onset, Scrit, as a function of temperature and dust composition. Using infrared spectroscopy to monitor ice nucleation and growth, we find a significant barrier to ice formation, with a pronounced temperature dependence. Even on clay minerals which show uptake of non-crystalline water before ice nucleation, we find a saturation ratio of 2.5 or more (RHice > 250%) is needed to begin ice growth at temperatures near 160 K. These results could lead to changes of four orders of magnitude in the nucleation rate relative to the presumptions used currently in Mars microphysical models, which commonly set the contact parameter, m, to a single value of 0.95. Our results range from m = 0.84 to m = 0.98. For ice nucleation on Arizona Test Dust, the temperature dependence is described by m = 0.0046 * Tnucl + 0.1085, while m = 0.0055 * Tnucl + 0.0003 on a smectite-rich clay sample. Our findings suggest that cloud formation will be more difficult than previously thought, potentially leading to areas of increased near-surface humidity but generally drier conditions in the atmosphere of Mars, overall.  相似文献   

19.
Hydrated minerals on Mars are most commonly found in ancient terrains dating to the first billion years of the planet’s evolution. Here we discuss the identification of a hydrated light-toned rock unit present in one Chasma of the Noctis Labyrinthus region. Stratigraphy and topography show that this alteration layer is part of a thin unit that drapes pre-existing bedrock. CRISM spectral data show that the unit contains hydrated minerals indicative of aqueous alteration. Potential minerals include sulfates such as bassanite (CaSO4·1/2H2O) or possibly hydrated chloride salts. The proximity of a smooth volcanic plain and the similar crater model age (Late Amazonian, <100 Myr) of this plain and the draping deposits suggest that the alteration layer may be formed by the interaction of water with ash layers deposited during this geologically recent volcanic activity. The alteration phases may have formed due to the presence of snow in contact with hot ash, or eventually solid-gas interactions due to the volcanic activity. The relatively young age of the volcanic plain implies that recent alteration processes have occurred on Mars in relation with volcanic activity, but such local processes do not require conditions different than the current climate.  相似文献   

20.
We study the propagation of gravity waves in the martian atmosphere using a linearized one-dimensional full-wave model. Calculations are carried out for atmospheric parameters characteristic of Mars Orbiter Laser Altimeter (on Mars Global Surveyor MGS) observations of apparent gravity waves in high latitude clouds and MGS radio occultation measurements of temperature variations with height suggestive of gravity wave activity. Waves that reach the thermosphere produce fluctuations in density comparable in amplitude with the density variations detected in Mars Odyssey aerobraking data. Gravity waves of modest amplitude are found to deposit momentum and generate significant heating and cooling in the martian atmosphere. The largest heating and cooling effects occur in the thermosphere, at altitudes between about 130 and 150 km, with heating occurring at the lower altitudes and cooling taking place above.  相似文献   

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