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1.
The surface composition of Europa is of special interest due to the information it might provide regarding the presence of a subsurface ocean. One source of this information is the infrared reflectance spectrum. Certain surface regions of Europa exhibit distorted H2O vibrational overtone bands in the 1.5 and 2.0 μm region, as measured by the Galileo mission Near Infrared Mapping Spectrometer (NIMS). These bands are clearly the result of highly concentrated solvated contaminants. However, two interpretations of their identity have been presented. One emphasizes hydrated salt minerals and the other sulfuric acid, although each does not specifically rule out some of the other. It has been pointed out that accurate chemical identification of the surface composition must depend on integrating spectral data with geochemical models, and information on the tenuous atmosphere sputtered from the surface. It is also extremely important to apply detailed chemistry when interpreting the spectral data, including knowledge of mineral dissolution chemistry and the subsequent optical signatures of ion solvation in low-temperature ice. We present studies of flash frozen acid and salt mixtures as Europa surface analogs and demonstrate that solvated protons, metal cations and inorganic anions all influence the spectra and must all, collectively, be considered when assigning Europa spectral features. These laboratory data show best correlation with NIMS Europa spectra for multi-component mixtures of sodium and magnesium bearing sulfate salts mixed with sulfuric acid. The data provide a concentration upper bound of 50-mol% for MgSO4 and 40-mol% for Na2SO4. This newly reported higher sodium and proton content is consistent with low-temperature aqueous differentiation and hydrothermal processing of carbonaceous chondrite-forming materials during the formation and early evolution of Europa.  相似文献   

2.
M.H. Moore  R.L. Hudson 《Icarus》2007,189(2):409-423
Spectra of Europa, Ganymede, and Callisto reveal surfaces dominated by frozen water, hydrated materials, and minor amounts of SO2, CO2, and H2O2. These icy moons undergo significant bombardment by jovian magnetospheric radiation (protons, electrons, and sulfur and oxygen ions) which alters their surface compositions. In order to understand radiation-induced changes on icy moons, we have measured the mid-infrared spectra of 0.8 MeV proton-irradiated SO2, H2S, and H2O-ice mixtures containing either SO2 or H2S. Samples with H2O/SO2 or H2O/H2S ratios in the 3-30 range have been irradiated at 86, 110, and 132 K, and the radiation half-lives of SO2 and H2S have been determined. New radiation products include the H2S2 molecule and HSO−3, HSO−4, and SO2−4 ions, all with spectral features that make them candidates for future laboratory work and, perhaps, astronomical observations. Spectra of both unirradiated and irradiated ices have been recorded as a function of temperature, to examine thermal stability and phase changes. The formation of hydrated sulfuric acid in irradiated ice mixtures has been observed, along with the thermal evolution of hydrates to form pure sulfuric acid. These laboratory studies provide fundamental information on likely processes affecting the outer icy shells of Europa, Ganymede, and Callisto.  相似文献   

3.
Europa's surface is chemically altered by radiolysis from energetic charged particle bombardment. It has been suggested that hydrated sulfuric acid (H2SO4·nH2O) is a major surface species and is part of a radiolytic sulfur cycle, where a dynamic equilibrium exists between continuous production and destruction of sulfur polymers Sx, sulfur dioxide SO2, hydrogen sulfide H2S, and H2SO4·nH2O. We measured the rate of sulfate anion production for cyclo-octal sulfur grains in frozen water at temperatures, energies, and dose rates appropriate for Europa using energetic electrons. The measured rate is GMixture(SO42−)=fSulfur (r0/r)βG1 molecules (100 eV)−1, where fSulfur is the sulfur weight fraction, r is the grain radius, r0=50 μm, β≈1.9, and G1=0.4±0.1. Equilibrium column densities N are derived for Europa's surface and follow the ordering N(H2SO4) » N(S)>N(SO2)>N(H2S). The lifetime of a sulfur atom on Europa's surface for radiolysis to H2SO4 is τ(−S)=120(r/r0)β years. Rapid radiolytic processing hides the identity of the original source of the sulfurous material, but Iogenic plasma ion implantation and an acidic or salty ocean are candidate sources. Sulfate salts, if present, would be decomposed in <3800 years and be rapidly assimilated into the sulfur cycle.  相似文献   

4.
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   

5.
The formation of hydrated salts is an expected consequence of aqueous alteration of Main Belt objects, particularly for large, volatile‐rich protoplanets like Ceres. Sulfates, present on water‐bearing planetary bodies (e.g., Earth, Mars, and carbonaceous chondrite parent bodies) across the inner solar system, may contribute to Ceres’ UV and IR spectral signature along with phyllosilicates and carbonates. We investigate the presence and stability of hydrated sulfates under Ceres’ cryogenic, low‐pressure environment and the consequent spectral effects, using UV–Vis–IR reflectance spectroscopy. H2O loss begins instantaneously with vacuum exposure, measured by the attenuation of spectral water absorption bands, and a phase transition from crystalline to amorphous is observed for MgSO4·6H2O by X‐ray powder diffraction. Long‐term (>40 h), continuous exposure of MgSO4·nH2O (n = 0, 6, 7) to low pressure (10?3–10?6 Torr) causes material decomposition and strong UV absorption below 0.5 μm. Our measurements suggest that MgSO4·6H2O grains (45–83 μm) dehydrate to 2% of the original 1.9 μm water band area over ~0.3 Ma at 200 K on Ceres and after ~42 Ma for 147 K. These rates, inferred from an Avrami dehydration model, preclude MgSO4·6H2O as a component of Ceres’ surface, although anhydrous and minimally hydrated sulfates may be present. A comparison between Ceres emissivity spectra and laboratory reflectance measurements over the infrared range (5–17 μm) suggests sulfates cannot be excluded from Ceres’ mineralogy.  相似文献   

6.
Sulfurous acid (H2SO3) has never been characterized or isolated on Earth. This is caused by the unfavorable conditions for H2SO3 within Earth's atmosphere due to the high temperatures, the high water content and the oxidizing environment. Kinetic investigations by means of transition state theory showed that the half-life of H2SO3 at 300 K is 1 day but at 100 K it is increased to 2.7 billion years. Natural conditions to form H2SO3 presumably require cryogenic SO2 or SO2/H2O mixtures and high energy proton irradiation at temperatures around 100 K. Such conditions can be found on the Jupiter moons Io and Europa. Therefore, we calculated IR-spectra of H2SO3 which we compared with Galileo's spectra of Io and Europa. From the available data we surmise that H2SO3 is present on Io and probably but to a smaller extent on Europa.  相似文献   

7.
Ryo Nakamura  Eiji Ohtani 《Icarus》2011,211(1):648-654
We have determined the phase relation of the MgSO4-H2O binary system using an externally heated diamond anvil cell in the compositional range of 0-30 wt.% MgSO4, and under temperature and pressure conditions from 298 to 500 K and up to 4.5 GPa. Using our experimental results, we were able to estimate the composition of the ice mantle of the large icy satellites of Jupiter, such as Ganymede.In our experiments, we identified the following phases in the MgSO4-H2O system up to 4 GPa at 298 K: Ices VI and VII, magnesium heptahydrate, MgSO4·7H2O, and a liquid phase. The present phase relations suggest that there may be a deep internal ocean down to a depth about 800 km in the interior of Ganymede.  相似文献   

8.
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   

9.
We report laboratory studies on the 0.8 MeV proton irradiation of ices composed of sulfuric acid (H2SO4), sulfuric acid monohydrate (H2SO4·H2O), and sulfuric acid tetrahydrate (H2SO4·4H2O) between 10 and 180 K. Using infrared spectroscopy, we identify the main radiation products as H2O, SO2, (S2O3)x, H3O+, , and . At high radiation doses, we find that H2SO4 molecules are destroyed completely and that H2SO4·H2O is formed on subsequent warming. This hydrate is significantly more stable to radiolytic destruction than pure H2SO4, falling to an equilibrium relative abundance of 50% of its original value on prolonged irradiation. Unlike either pure H2SO4 or H2SO4·H2O, the loss of H2SO4·4H2O exhibits a strong temperature dependence, as the tetrahydrate is essentially unchanged at the highest irradiation temperatures and completely destroyed at the lowest ones, which we speculate is due to a combination of radiolytic destruction and amorphization. Furthermore, at the lower temperatures it is clear that irradiation causes the tetrahydrate spectrum to transition to one that closely resembles the monohydrate spectrum. Extrapolating our results to Europa’s surface, we speculate that the variations in SO2 concentrations observed in the chaotic terrains are a result of radiation processing of lower hydration states of sulfuric acid and that the monohydrate will remain stable on the surface over geological times, while the tetrahydrate will remain stable in the warmer regions but be destroyed in the colder regions, unless it can be reformed by other processes, such as thermal reactions induced by diurnal cycling.  相似文献   

10.
Due to the discovery of the evaporitic environment on the Martian surface, there is a reasonable possibility that evaporites served (or still serve) as habitats for microbial life if ever present on Mars. At the very least, if no signatures of extant life exist within these rocks, it may sustain molecular remnants as evidence for living organisms in the past. β-Carotene, among other carotenoids, could be such a suitable biomarker. In this study, Raman micro-spectroscopy was tested as a nondestructive method of determining the presence of β-carotene in experimentally prepared evaporitic matrices. Samples prepared by mixing β-carotene with powdered gypsum (CaSO4·2H2O), halite (NaCl) and epsomite (MgSO4·7H2O) were analyzed using a 785 nm excitation source. Various concentrations of β-carotene in the matrices were investigated to determine the lowest β-carotene content detectable by Raman micro-spectroscopy. Mixtures were also measured with a laser beam permeating the crystals of gypsum and epsomite in order to evaluate the possibility of identifying β-carotene inside the mineral matrix.We were able to obtain a clear β-carotene signal at the 10 mg kg−1 concentration level—the number of registered β-carotene Raman bands differed depending on the particular mineral matrix. Spectral signatures of β-carotene were detected even when analyzing samples containing 1 mg kg−1 of this molecule. The 10-100 mg kg−1 of β-carotene in mineral matrices (halite, epsomite) was detected when analyzed through the monocrystal of gypsum and epsomite, respectively. These results will aid both in-situ analyses on Mars and sample analyses on Earth.  相似文献   

11.
Europa is bombarded by intense radiation that erodes the surface, launching molecules into a thin “atmosphere” representative of surface composition. In addition to atoms and molecules created in the mostly water ice surface such as H2O, O2, H2, the atmosphere is known to have species representative of trace surface materials. These trace species are carried off with the 10-104 H2O molecules ejected by each energetic heavy ion, a process we have simulated using molecular dynamics. Using the results of those simulations, we found that a neutral mass spectrometer orbiting ∼100 km above the surface could detect species with surface concentrations above ∼0.03%. We have also modeled the atmospheric spatial structure of the volatile species CO2 and SO2 under a variety of assumptions. Detections of these species with moderate time and space resolution would allow us to constrain surface composition, chemistry and to study space weathering processes.  相似文献   

12.
The goal of this work is to determine the spectroscopic properties of sulfate in martian soil analogs over the wavelength range 0.3 to 25 μm (which is relevant to existing and planned remotely sensed data sets for Mars). Sulfate is an abundant component of martian soil (up to 9% SO3 by weight) and apparently exists as a particulate in the soil but also as a cement. Although previous studies have addressed the spectroscopic identity of sulfates on Mars, none have used laboratory mixtures of materials with sulfates at the abundances measured by landed spacecraft, nor have any works considered the effect of salt-cementation on spectral properties of soil materials. For this work we created mixtures of a palagonitic soil (JSC Mars-1) and sulfates (MgSO4 and CaSO4·2H2O). The effects of cementation were determined and separated from the effects of packing and hydration by measuring the samples as loose powders, packed powders, cemented materials, and disaggregated materials. The results show that the presence of particulate sulfate is best observed in the 4-5 μm region. Soils cemented with sulfate exhibit a pronounced restrahlen band between 8 and 9 μm as well as well-defined absorptions in the 4-5 μm region. Cementation effects are distinct from packing effects and disaggregation of cemented samples rapidly diminishes the strength of the restrahlen bands. The results of this study show that sulfate in loose materials is more detectable in the near infrared (4-5 μm) than in the thermal infrared (8-9 μm). However, cemented materials are easily distinguished from loose mixtures in the thermal infrared because of the high values of their absorption coefficient in this region. Together these results suggest that both wavelength regions are important for determining the spatial extent and physical form of sulfates on the surface of Mars.  相似文献   

13.
This investigation uses linear mixture modeling employing cryogenic laboratory reference spectra to estimate surface compositions and water ice grain sizes of Europa’s ridged plains and smooth low albedo plains. Near-infrared spectra for 23 exposures of ridged plains materials are analyzed along with 11 spectra representing low albedo plains. Modeling indicates that these geologic units differ both in the relative abundance of non-ice hydrated species and in the abundance and grain sizes of water ice. The background ridged plains in our study area appear to consist predominantly of water ice (∼46%) with approximately equal amounts (on average) of hydrated sulfuric acid (∼27%) and hydrated salts (∼27%). The solutions for the smooth low albedo plains are dominated by hydrated salts (∼62%), with a relatively low mean abundance of water ice (∼10%), and an abundance of hydrated sulfuric acid similar to that found in ridged plains (∼27%). The model yields larger water ice grain sizes (100 μm versus 50-75 μm) in the ridged plains. The 1.5-μm water ice absorption band minimum is found at shorter wavelengths in the low albedo plains deposits than in the ridged plains (1.498 ± .003 μm versus 1.504 ± .001 μm). The 2.0-μm band minimum in the low albedo plains exhibits a somewhat larger blueshift (1.964 ± .006 μm versus 1.983 ± .006 μm for the ridged plains).The study area spans longitudes from 168° to 185°W, which includes Europa’s leading side-trailing side boundary. A well-defined spatial gradient of sulfuric acid hydrate abundance is found for both geologic units, with concentrations increasing in the direction of the trailing side apex. We associate this distribution with the exogenic effects of magnetospheric charged particle bombardment and associated chemical processing of surface materials (the radiolytic sulfur cycle). However, one family of low albedo plains exposures exhibits sulfuric acid hydrate abundances up to 33% lower than found for adjacent exposures, suggesting that these materials have undergone less processing, thus implying that these deposits may have been emplaced more recently.Modeling identifies high abundances (to 30%) of magnesium sulfate brines in the low albedo plains exposures. Our investigation marks the first spectroscopic identification of MgSO4 brine on Europa. We also find significantly higher abundances of sodium-bearing species (bloedite and mirabilite) in the low albedo plains. The results illuminate the role of radiolytic processes in modifying the surface composition of Europa, and may provide new constraints for models of the composition of Europa’s putative subsurface ocean.  相似文献   

14.
We report the results from a systematic laboratory investigation on the fundamental properties of hydrous ferric sulfates. The study involves 150 experiments with duration of over 4 years on the stability field and phase transition pathways under Mars relevant environmental conditions for five ferric sulfates: ferricopiapite [Fe4.67(SO4)6(OH)2·20H2O], kornelite [Fe2(SO4)3·7H2O], a crystalline and an amorphous pentahydrated ferric sulfate [Fe2(SO4)3·5H2O], and rhomboclase [FeH(SO4)2·4H2O]. During the processes of phase transitions, we observed the phenomena that reflect fundamental properties of these species and the occurrence of other common hydrous ferric sulfates, e.g. paracoquimbite [Fe2(SO4)3·9H2O]. Based on the results of this set of experiments, we have drown the boundaries of deliquescence zone of five hydrous ferric sulfates and estimated the regions of their stability field in temperature (T) – relative humidity (RH) space. Furthermore, we selected the experimental parameters for a next step investigation, which is to determine the location of the phase boundary between two solid ferric sulfates, kornelite [Fe2(SO4)3·7H2O] and pentahydrated ferric sulfate [Fe2(SO4)3·5H2O]. The experimental observations in ferricopiapite dehydration processes were used to interpret the observed spectral change of Fe-sulfate-rich subsurface soils on Mars after their exposure by the Spirit rover to current martian atmospheric conditions.  相似文献   

15.
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   

16.
M. Parente  J.L. Bishop 《Icarus》2009,203(2):421-436
The objective of this work is to propose an automated unmixing technique for the analysis of 11-channel Mars Exploration Rover Panoramic Camera (MER/Pancam) spectra. Our approach is to provide a screening tool for identifying unique/distinct reflectance spectra. We demonstrate the utility of this unmixing technique in a study of the mineralogy of the bright salty soils exposed by the rover wheels in images of Gusev crater regions known as Paso Robles (Sols 400,426), Arad (Sol 721), and Tyrone (Sol 790). The unmixing algorithm is based on a novel derivation of the Nonnegative Matrix Factorization technique and includes added features that preclude the adverse effects of low abundance materials that would otherwise skew the unmixing. In order to create a full 11-channel spectrum out of the left and right eye stereo pairs, we also developed a new registration procedure that includes rectification and disparity calculation of the images. We identified two classes of endmember spectra for the bright soils imaged on Sols 426 and 790. One of these endmember classes is also observed for soils imaged on Sols 400 and 721 and has a unique spectral shape that is distinct from most iron oxide, sulfate and silicate spectra and differs from typical martian surface spectra. Instead, its unique spectral character resembles the spectral shape of the ferric sulfate minerals fibroferrite (Fe3+(SO4)(OH) · 5H2O) and ferricopiapite and the phosphate mineral ferristrunzite . The other endmember class is less consistent with specific minerals and is likely a mixture of altered volcanic material and some bright salts. Further analyses of data from Sols 400 and 790 using an anomaly detection algorithm as a tool for detecting low abundance materials additionally suggests the identification of the sulfate mineral paracoquimbite (Fe2(SO4)3 · 9H2O). This spectral study of Pancam images of the bright S- and P-enriched soils of Gusev crater identifies specific ferric sulfate and ferric phosphate minerals that are consistent with the unique spectral properties observed here in the 0.4-1 μm range.  相似文献   

17.
We present new experimental results on impact shock chemistry into icy satellites of the outer planets. Icy mixtures of pure water ice with CO2, Na2CO3, CH3OH, and CH3OH/(NH4)2SO4 at 77 K were ablated with a powerful pulsed laser—a new technique used to simulate shock processes which can occur during impacts. New products were identified by GC-MS and FTIR analyses after laser ablation. Our results show that hydrogen peroxide is formed in irradiated H2O/CO2 ices with a final concentration of 0.23%. CO and CH3OH were also detected as main products. The laser ablation of frozen H2O/Na2CO3 generates only CO and CO2 as destruction products from the salt. Pulsed irradiation of water ice containing methanol leads also to the formation of CO and CO2, generates methane and more complex molecules containing carbonyl groups like acetaldehyde, acetone, methyl formate, and a diether, dimethyl formal. The last three compounds are also produced when adding ammonium sulfate to H2O/CH3OH ice, but acetone is more abundant. The formation of two hydrocarbons, CH4 and C2H6 is observed as well as the production of three nitrogen compounds, nitrous oxide, hydrogen cyanide, and acetonitrile.  相似文献   

18.
The available full-disk reflectance spectra of Io in the range 0.3 to 2.5 μm have been interpreted by comparison with new laboratory spectra of a wide variety of natural and synthetic mineral phases in order to determine a surface compositional model for Io that is consistent with Io's other known chemical and physical properties. Our results indicate that the dominant mineral phases are sulfates and free sulfur derived from them, which points toward a low temperature and initially water-rich surface assemblage. Our current preferred mineral phase mixture that best matches the Io data and is simultaneously most consistent with other constraints, consists of a fine-grained particulate mixture of free sulfur (55 vol%), dehydrated bloedite [Na2Mg(SO4)2·xH2O] (30 vol%) ferric sulfate [Fe2(SO4)3·xH2O] (15 vol%), and trace amounts of hematite [Fe2O3]. Other salts may be present, such as halite and sodium nitrate, as well as clay minerals. Such a model is consistent with a probable pre- and post-accretion thermal history of Io-forming material and Io's observed Na emission and other properties. These results further support the evaporite surface hypothesis of Fanale et al'; while not precluding the presence of certain silicate phases such as montmorillonite.The average surface of Io's leading hemisphere appears to contain less free sulfur and more salts and to be finer grained than that of the trailing hemisphere. Since Io is immersed in Jupiter's magnetosphere, irradiation damage effects from low-energy proton bombardment were studied. Irradiation damage of lattices is estimated to be a relatively minor but operative process on the surface of Io; irradiation darkening by sulfate reduction to free sulfur and by F-center production in salts may be partly responsible for the differences in albedo of leading and trailing hemispheres and equatorial and polar regions of Io, but slight regional differences in relative intrinsic phase concentration on the surface may likewise account for these global variations in albedo.Possible unusual surface properties predicted by this model include: posteclipse darkening in certain wavelenghts, limb brightening in certain wavelengths, and unusual surface electrical properties. Further refinement of Io's surface composition model and better understanding of surface irradiation effects will be possible when observational data in the range 0.20 to 0.30 μm are obtained and when improved spectra in the range 0.30 to 5.0 μm are obtained having increased spectral, spatial, and temporal resolution.  相似文献   

19.
A thermodynamical analysis of the multicomponent system SiTiAlFeMnMgCaNaKPCHO open with respect to CO2, CO, H2O was carried out. Hydration and carbonatization processes are proposed to be geochemical consequences of the hypothesis of quasi-equilibrium conditions between the troposphere and crustal surface rocks. The probable rock-forming hydrated mineral phases are represented by epidote, glaucophane, tremolite, phlogopite, and annite; the carbonatization results in existence of calcite and dolomite as rock-forming minerals of weathered alkaline lavas. The surface rocks are assumed to have high ferric/ferrous iron ratios. The wollastonite equilibrium is rejected as a buffering chemical reaction. Hydrated minerals could be stable at least up to 5-km depths and contribute about 0.1 × 1024 g of H2O whereas about (0.7–0.8) × 1024 g of H2O would be consumed in ferrous iron oxidation with concomitant hydrogen dissipation. The distribution of H2O in the outer planetary shells is possibly a function of their temperatures.  相似文献   

20.
The exosphere of an atmosphereless icy moon is the result of different surface release processes and subsequent modification of the released particles. At Europa icy moon, water molecules are directly released, but photolysis and radiolysis due to solar UV and Jupiter’s magnetospheric plasma, respectively, can result in OH, H, O and (possibly) H2 production. These molecules can recombine to reform water and/or new chemical species. As a consequence, Europa’s neutral environment becomes a mixture of different molecules, among which, H2O dominates in the highest altitudes and O2, formed mainly by radiolysis of ice and subsequent release of the produced molecules, prevails at lower altitudes. In this work, starting from a previously developed Monte Carlo model for the generation of Europa’s exosphere, where the only considered species was water, we make a first attempt to simulate also the H2 and O2 components of the neutral environment around Europa, already observed by the Hubble Space Telescope and the Ultraviolet Imaging Spectrograph on board Cassini, during its flyby of Jupiter. Considering a specific configuration where the leading hemisphere coincides with the sunlit hemisphere, we estimate along the Europa–Sun line an O2 column density of about 1.5 × 1019 m?2 at the dayside and 3 × 1018 m?2 at the nightside. In this work we also improve our previous estimation of the sputtered H2O exosphere of this moon, taking into consideration the trailing–leading asymmetry in the magnetospheric ion bombardment and the energy and temperature dependences of the process yields. We find that a density of 1.5 × 1012 H2O/m3 is expected at altitudes ～0.1RE above the surface of the trailing hemisphere. Additionally, we calculate the escape of H2O, O2 and H2. The total number of neutral atoms in Europa’s neutral torus, is estimated to be in the range 7.8 × 1032–3.3 × 1033.  相似文献   

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