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1.
MicrOmega is an ultra miniaturized spectral microscope for in situ analysis of samples. It is composed of 2 microscopes; one with a spatial sampling less or equal to 4 μm, working in 4 colors in the visible range: MicrOmega/VIS, and a NIR hyperspectral microscope working in the spectral range 0.9–4 μm with a spatial sampling of 20 μm per pixel: MicrOmega/IR (described in this paper). MicrOmega/IR illuminates and images samples a few mm in size and acquires the NIR spectrum of each resolved pixel in up to 320 contiguous spectral channels. The goal of this instrument is to analyze in situ the composition of collected samples at almost their grain size scale, in a non-destructive way. With the chosen spectral range and resolution, a wide variety of constituents can be identified: minerals, such as pyroxene and olivine, ferric oxides, hydrated phyllosilicates, sulfates and carbonates and ices and organics. The composition of the various phases within a given sample is a critical record of its formation and evolution. Coupled to the mapping information, it provides unique clues to describe the history of the parent body (planet, satellite and small body). In particular, the capability to identify hydrated grains and to characterize their adjacent phases has a huge potential in the search for possible bio-relics.  相似文献   

2.
Chemical analyses of soil samples performed at different landing sites on Mars suggest the presence of sulfate minerals. These minerals are also thought to be present in the globally mixed Martian bright soils covering large areas of the planet. However, remote soil spectra have so far provided only tentative identification of sulfates regarding mineral types and abundances. This paper concentrates on the detectability of four Ca- and Mg-sulfates (anhydrite, gypsum, kieserite, hexahydrite) in the 4–5 μm range of Martian remote soil spectra. This spectral range is important for sulfate detection as most fine-grained sulfates exhibit significant absorption bands between 4 and 5 μm, independent of the texture of the host soils (e.g., loose powdered or cemented soils). Furthermore, this is the spectral range for which the Planetary Fourier Spectrometer (PFS) and Observatoire pour la Minéralogie, l’Eau, les Glaces, et l’Activité (OMEGA) instruments onboard ESA/Mars Express mission provide high spectral and spatial resolution data. Laboratory near- and mid-IR reflectance spectra of the pure sulfates and their mixtures with a terrestrial Martian soil analog were acquired. The results show that even the smallest amount of admixed sulfate (∼5 wt%) generates significant absorption features in the portion of the 4–5 μm range not covered by the saturated Martian atmospheric CO2 absorption band between 4.2 and 4.4 μm. Model calculations of the influence of emitted surface radiation on the detectability of sulfate features show that the depth of the features decreases strongly with increasing surface temperature of an observed area resulting in the fact that all sulfates are spectrally hidden at surface temperatures around 270 K even at ∼14 or ∼25 wt% sulfate content in the soils. Sulfates become increasingly detectable depending on the sulfate content if the surface temperature is below 260 K. The outcome of this work helps to constrain the conditions needed for remote detection of sulfates within Martian bright soils in the 4–5 μm range.  相似文献   

3.
Most phyllosilicates on Mars appear to be associated with ancient terrains. As such, they may have experienced shock heating produced by impacts and could have been significantly altered or melted. We characterized the effects of high temperatures on the mid-to-far-infrared (mid-to-far-IR) emission (100–1400 cm?1; 7.1–100 μm) and near-infrared (NIR) reflectance (1.2–2.5 μm) spectra of phyllosilicates by measuring experimentally calcined (100–900 °C) phyllosilicates and also two zeolites. Correlated differential scanning calorimetry (DSC) measurements were also performed on each sample to provide insight into the thermal activities of the phyllosilicates and natural zeolites. Our results indicate that all phyllosilicates exhibit characteristic degradations in both NIR and mid-to-far-IR spectral properties between 400 and 800 °C, mainly attributable to the dehydroxylation and recrystallization processes as temperature increases. Spectral features of natural zeolites persist to higher temperatures compared to features of phyllosilicates during heating treatments. The thermal behaviors of phyllosilicate infrared (IR) properties are greatly influenced by the compositions of the octahedral cations: (1) changes in both the NIR and mid-to-far-IR spectra of phyllosilicates tend to occur at lower temperatures (300–400 °C) in the Fe3+-rich samples as compared to the Al3+-rich types (400–600 °C); (2) Mg2+-trioctahedral phyllosilicates hectorite, saponite, and sepiolite all display major mid-to-far-IR spectral changes at 700 °C, corresponding to the formation of enstatite; (3) phyllosilicates that have minor replacement of Mg2+ for Al3+ in octahedral positions (e.g. cheto-type montmorillonite and palygorskite) show an absorption band at ～920 cm?1 that becomes strong at 900 °C. Inconsistency between spectral behaviors in the mid-to-far-IR and NIR regions is also discussed for phyllosilicates. Results from this study have provided suggestive evidence for the scenario that some phyllosilicates could lose all original spectral features in mid-to-far-IR region while maintaining their characteristic hydration bands in NIR region in the same temperature range.  相似文献   

4.
We present the Messinian evaporite suite (Mediterranean region) and the Solfatara hydrothermal system (Phlegraean Fields volcanic province, Italy), discuss their implications for understanding the origin of sulfates on Mars and show preliminary sets of VNIR laboratory and in situ reflectance spectra of rocks from these geologic systems. The choice was based on a number of evidence relative to Mars: (1) the chemistry of the Martian sulfates, suggesting fluid interactions with possibly alkali-basaltic rocks and/or regolith; (2) close range evidence of sulfates within sedimentary formations on Mars; (3) sulfate spectral signatures associated to large-scale layered patterns interpreted as thick depositional systems on Mars. The Messinian evaporites comprise three units: primary shallow-water sulfates (primary lower gypsum: PLG), shallow- to deep-water mixed sulfates and clastic terrigenous deposits (resedimented lower gypsum: RLG), and shallow-water associations of primary sulfates and clastic fluvio-deltaic deposits (upper evaporites: UE). The onset of the Messinian evaporites records the transition to negative hydrologic budget conditions associated with the Messinian Salinity Crisis, which affected the entire Mediterranean basin and lasted about 640 kyr. The Solfatara is a still evolving hydrothermal system that provides epithermal deposits precipitated from the interaction of fluids and trachybasaltic to phonolitic rocks. Thermal waters include alkali-chloride, alkali-carbonate and alkali-sulfate endmembers.The wide spectrum of sedimentary gypsum facies within the Messinian formation includes some of the depositional environments hitherto identified on Mars and others not found on Mars. The PLG unit includes facies associations correlated over long distances, that could be a possible analog of the stratified rock units exposed from Arabia Terra at least as far as Valles Marineris. The facies cycles within the UE unit can be compared to the sequences of strata observed in craters such as Holden and Eberswalden. The UE unit records paleoenvironmental changes which are ultimately controlled by terrestrial climatic variations. They can be considered as a reliable climatic proxy and may be useful for the reconstruction of climatic events on Mars. The intermediate Messinian RLG unit has not, at present, a well-defined depositional counterpart on Mars, although there are some similarities with the northern lowlands and Vastitas Borealis Formation. The dramatic variation of hydrologic budget conditions at the onset of the Messinian evaporites may provide criteria for the interpretation of similar variations on Mars.The volcanic rocks at the Solfatara bear some similarities with the “alkaline magmatic province” observed at the Gusev crater on Mars, and the assemblages of hydrothermal phases resulting from the Solfatara's parent rocks could be analogues for processes involving Gusev-type rocks.The Messinian sulfates have a prevalent Ca-sulfatic composition and wide textural variability. Preliminary laboratory reflectance spectra of rock samples in the VNIR region reveal the signature of sulfates and mixtures of several Fe-bearing phases. At the Solfatara, in situ reflectance measurements of epithermal minerals close to active fumaroles showed the presence of Fe-bearing sulfates, hematite, Al- and K-sulfates and abundant amorphous fraction. XRD analysis supported this interpretation.The range of depositional facies observed in the Messinian units and the variety of minerals detected in the Solfatara will be useful for the interpretation of close range data of Mars. The spectral characterization at various scales of the Messinian sedimentary facies and the Solfatara hydrothermal minerals will both help in the exploration of Mars from orbit and with close range inspection.  相似文献   

5.
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   

6.
Previous orbital mapping of crystalline gray haematite, ferric oxides, and sulfates has shown an association of this mineralogy with light-toned, layered deposits on the floor of Valles Marineris, in chaos terrains in the canyon’s outflow channels, and in Meridiani Planum. The exact nature of the relationship between ferric oxides and sulfates within Valles Marineris is uncertain. The Observatoire pour la Mineralogie, l’Eau, les Glaces et l’Activite (OMEGA) spectrometer initially identified sulfate and ferric oxides in the layered deposits of Valles Marineris. The Thermal Emission Spectrometer (TES) has also mapped coarse (gray) haematite in or at the base of these deposits. We use Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) spectra and Context Camera (CTX) and High Resolution Imaging Science Experiment (HiRISE) imagery from the Mars Reconnaissance Orbiter (MRO) to explore the mineralogy and morphology of the large layered deposit in central Capri Chasma, part of the Valles Marineris canyon system that has large, clear exposures of sulfate and haematite. We find kieserite (MgSO4·H2O) and ferric oxide (often crystalline red haematite) in the lower bedrock exposures and a polyhydrated sulfate without ferric oxides in the upper bedrock. This stratigraphy is duplicated in many other basinal chasmata, suggesting a common genesis. We propose the haematite and monohydrated sulfate formed by diagenetic alteration of a sulfate-rich sedimentary deposit, where the upper polyhydrated sulfate-rich, haematite-poor layers either were not buried sufficiently to convert to a monohydrated sulfate or were part of a later depositional phase. Based on the similarities between the Valles Marineris assemblages and the sulfate and haematite-rich deposits of Meridiani Planum, we hypothesize a common evaporite and diagenetic formation process for the Meridiani Planum sediments and the sulfate-bearing basinal Interior Layered Deposits.  相似文献   

7.
We investigate the sulfate and iron oxide deposits in Ophir Chasma, Mars, based on short-wave infrared data from the Compact Reconnaissance Imaging Spectrometer for Mars - CRISM and from the Observatoire pour la Minéralogie, l’Eau, les Glaces et l’Activité - OMEGA. Sulfates are detected mainly in two locations. In the valley between Ophir Mensa and the southern wall of Ophir Chasma, kieserite is found both within the slope of Ophir Mensa, and superposed on the basaltic wall of the chasm. Here, kieserite is unconformably overlain by polyhydrated sulfate deposits and iron oxides. Locally, jarosite and unidentified phases with absorptions at 2.21 μm or 2.23 μm are detected, which could be mixtures of jarosite and amorphous silica or other poorly crystalline phases.The second large sulfate-rich outcrop is found on the floor of the central valley. Although the same minerals are found here, polyhydrated sulfates, kieserite, iron oxides, and locally a possibly jarosite-bearing phase, this deposit is very distinct. It is not layered, almost horizontal, and located at a much lower elevation of below −4250 m. Kieserite superposes polyhydrated sulfate-rich deposits, and iron oxides form lags.The facies of sulfate formation remains unclear, and could be different for the two locations. A formation in a lake, playa or under a glacier is consistent with the mineralogy of the central valley and its flat, low-lying topography. This is not conceivable for the kieserite deposits observed south of Ophir Mensa. These deposits are observed over several thousands of meters of elevation, which would require a standing body of water several thousands of meters deep. This would have lead to much more pervasive sulfate deposits than observed. These deposits are therefore more consistent with evaporation of groundwater infiltrating into previously sulfate-free light-toned deposits. The overlying polyhydrated sulfates and other mineral phases are observed in outcrops on ridges along the slopes of the southern chasm wall, which are too exposed to be reached by groundwater. Here, a water supply from the atmosphere by rain, snow, fog or frost is more conceivable.  相似文献   

8.
Analysis of visible to near infrared reflectance data from the MRO CRISM hyperspectral imager has revealed the presence of an ovoid-shaped landform, approximately 3 by 5 km in size, within the layered terrains surrounding the Mawrth Vallis outflow channel. This feature has spectral absorption features consistent with the presence of the ferric sulfate mineral jarosite, specifically a K-bearing jarosite (KFe3(SO4)2(OH)6). Terrestrial jarosite is formed through the oxidation of iron sulfides in acidic environments or from basaltic precursor minerals with the addition of sulfur. Previously identified phyllosilicates in the Mawrth Vallis layered terrains include a basal sequence of layers containing Fe-Mg smectites and an upper set of layers of hydrated silica and aluminous phyllosilicates. In terms of its fine scale morphology revealed by MRO HiRISE imagery, the jarosite-bearing unit has fracture patterns very similar to that observed in Fe-Mg smectite-bearing layers, but unlike that observed in the Al-bearing phyllosilicate unit. The ovoid-shaped landform is situated in an east-west bowl-shaped depression superposed on a north sloping surface. Spectra of the ovoid-shaped jarosite-bearing landform also display an anomalously high 600 nm shoulder, which may be consistent with the presence of goethite and a 1.92 μm absorption which could indicate the presence of ferrihydrite. Goethite, jarosite, and ferrihydrite can be co-precipitated and/or form through transformation of schwertmannite, both processes generally occurring under low pH conditions (pH 2-4). To date, this location appears to be unique in the Mawrth Vallis region and could represent precipitation of jarosite in acidic, sulfur-rich ponded water during the waning stages of drying.  相似文献   

9.
E.A. Cloutis  P. Hudon  T. Hiroi  M.J. Gaffey 《Icarus》2012,217(1):389-407
Powdered samples of a suite of 14 CR and CR-like chondrites, ranging from petrologic grade 1 to 3, were spectrally characterized over the 0.3–2.5 μm interval as part of a larger study of carbonaceous chondrite reflectance spectra. Spectral analysis was complicated by absorption bands due to Fe oxyhydroxides near 0.9 μm, resulting from terrestrial weathering. This absorption feature masks expected absorption bands due to constituent silicates in this region. In spite of this interference, most of the CR spectra exhibit absorption bands attributable to silicates, in particular an absorption feature due to Fe2+-bearing phyllosilicates near 1.1 μm. Mafic silicate absorption bands are weak to nonexistent due to a number of factors, including low Fe content, low degree of silicate crystallinity in some cases, and presence of fine-grained, finely dispersed opaques. With increasing aqueous alteration, phyllosilicate: mafic silicate ratios increase, resulting in more resolvable phyllosilicate absorption bands in the 1.1 μm region. In the most phyllosilicate-rich CR chondrite, GRO 95577 (CR1), an additional possible phyllosilicate absorption band is seen at 2.38 μm. In contrast to CM spectra, CR spectra generally do not exhibit an absorption band in the 0.65–0.7 μm region, which is attributable to Fe3+–Fe2+ charge transfers, suggesting that CR phyllosilicates are not as Fe3+-rich as CM phyllosilicates. CR2 and CR3 spectra are uniformly red-sloped, likely due to the presence of abundant Fe–Ni metal. Absolute reflectance seems to decrease with increasing degree of aqueous alteration, perhaps due to the formation of fine-grained opaques from pre-existing metal. Overall, CR spectra are characterized by widely varying reflectance (4–21% maximum reflectance), weak silicate absorption bands in the 0.9–1.3 μm region, overall red slopes, and the lack of an Fe3+–Fe2+ charge transfer absorption band in the 0.65–0.7 μm region.  相似文献   

10.
《Planetary and Space Science》2007,55(10):1328-1345
The planetary fourier spectrometer (PFS) for the Mars express mission (MEX) is an infrared spectrometer operating in the wavelength range from 1.2 to 45 μm by means of two spectral channels, called SWC (short wavelength channel) and LWC (long wavelength channel), covering, respectively, 1.2–5.5 and 5.5–45 μm.The middle-spring Martian north polar cap (Ls∼40°) has been observed by PFS/MEX in illuminated conditions during orbit 452. The SWC spectra are here used to study the cap composition in terms of CO2 ice, H2O ice and dust content. Significant spectral variation is noted in the cap interior, and regions of varying CO2 ice grain sizes, water frost abundance, CO2 ice cover and dust contamination can be distinguished. In addition, we correlate the infrared spectra with an image acquired during the same orbit by the OMEGA imaging spectrometer and with the altimetry from MOLA data. Many of the spectra variations correlate with heterogeneities noted in the image, although significant spectral variations are not discernible in the visible. The data have been divided into five regions with different latitude ranges and strong similarities in the spectra, and then averaged. Bi-directional reflectance models have been run with the appropriate lighting geometry and used to fit the observed data, allowing for CO2 ice and H2O ice grain sizes, dust and H2O ice contaminations in the form of intimate granular mixtures and spatial mixtures.A wide annulus of dusty water ice surrounds the recessing CO2 seasonal cap. The inner cap exhibits a layered structure with a thin CO2 layer with varying concentrations of dark dust, on top of an H2O ice underneath ground. In the best-fits, the ices beneath the top layer have been considered as spatial mixtures. The results are still very good everywhere in the spectral range, except where the CO2 ice absorption coefficients are such that even a thin layer is enough to totally absorb the incoming radiation (i.e. the band is saturated). This only happens around 3800 cm−1, inside the strong 2.7-μm CO2 ice absorption band. The effect of finite snow depth has been investigated through a layered albedo model. The thickness of the CO2 ice deposits increases with latitude, ranging from 0.5–1 g cm−2 within region II to 60–80 g cm−2 within the highest-latitude (up to 84°N) region V.Region I is at the cap edge and extends from 65°N to 72°N latitude. No CO2 ice is present in this region, which consists of relatively large grains of water ice (20 μm), highly contaminated by dust (0.15 wt%). The adjacent region II is a narrow region [76–79°N] right at the edge of the north residual polar cap. This region is very distinct in the OMEGA image, where it appears to surround the whole residual cap. The CO2 ice features are barely visible in these spectra, except for the strong saturated 2.7 μm band. It basically consists of a thin layer of 5-mm CO2 ice on top of an H2O ice layer with the same composition as region I. A third interesting region III is found all along the shoulder of the residual cap [79–81°N]. It extends over 1.5 km in altitude and over only 2° of latitude and consists of CO2 ice with a large dust content. It is an admixture of CO2 ice (3–4 mm), with several tens of ppm by mass of water ice and more than 2 ppt by mass of dust. The surface temperatures have been retrieved from the LWC spectra for each observation. We found an increase in the surface temperature in this region, indicating a spatial mixture of cold CO2 ice and warmer dust/H2O ice. Region IV is close to the top of the residual cap [81–84°N]; it is much brighter than region III, with a dust content 10 times lower than the latter. The CO2 grain size is 3 mm and strong CO2 ice features are present in the data, indicating a thicker CO2 ice layer than in region II (1–2 g cm−2). The final region V is right at the top of the residual cap (⩾84°N). It is “pure” CO2 ice (no dust) of 5 mm grain sizes, with 30 ppm by weight of water ice. The CO2 ice features are very pronounced and the 2.7 μm band is saturated. The optical thickness is close to the semi-infinite limit (30–40 g cm−2). Assuming a snowpack density of 0.5 g cm−3, we get a minimum thickness of 1–2 cm for the top-layer of regions II and III, 4–10 cm for region IV, and ⩾60–80 cm thickness for region V. These values are in close agreement with several recent results for the south seasonal polar cap.These results should provide new, useful constraints in models of the Martian climate system and volatile cycles.  相似文献   

11.
The extensive light-toned deposits in canyons and troughs in Valles Marineris provide evidence of formation through water-related processes. As such, these deposits offer a window to past conditions on Mars. We study a small outcrop of light-toned deposits in a closed trough in Coprates Catena, a chain of collapse pits to the south-east of the main Valles Marineris system. A well-exposed sequence of deposits on the base of the north wall of the trough offers a 220 m section for geochemical and morphologic analysis. Using CRISM data we identify the presence of both phyllosilicates and sulfates and/or opaline silica in the light toned deposits, which vary in relative strength with elevation. We observe a trend in the dominant mineralogical signal, with Al phyllosilicates occurring near the base of the deposits, both below and above a band of Fe/Mg phyllosilicates, before a transition to more sulfate- or opaline silica-rich material near the top of the section. This trend likely reflects a change in the chemistry of the water in which the deposits formed. Using a HiRISE Digital Elevation Model, we find that the layers in the light-toned deposits on both sides of the trough dip gently towards the center of the trough, with a dip direction that aligns with the strike of the trough, suggesting that the light-toned deposits formed after the trough. Our general morphologic and mineralogical observations fit well with significant amounts of water in the trough. The deposits are too small to be dated using crater counting techniques, however, our crater analysis suggests that the plains in which the trough formed are probably Late Hesperian in age. If the chemistry of the light-toned deposits reflects the primary depositional mineralogy, then this and other small troughs in Coprates Catena might provide evidence of limited phyllosilicate formation in this region towards the end of the Hesperian era on Mars.  相似文献   

12.
We identified 104 unique rock targets belonging to the olivine-rich Adirondack class using Mini-TES data. Rare rocks on the West Spur of the Columbia Hills and on the plains east of the Hills also belong to this class. We present evidence that Adirondack-class basaltic lavas may have had their origin at Apollinaris Tholus. Linear modeling of Adirondack-class rock spectra shows only minor variations in mineralogy and the primary phases identified are consistent with olivine basalt having an average olivine composition of ～Fo45. We used factor analysis and target transformation to identify variability within a single class of rocks for the first time, and we find that olivine abundance varies independently of a basaltic matrix. A spectral component previously attributed to downwelling radiance is proposed here to be attributable to optically thin dust on rocks, which has a greater effect on Mini-TES spectra than previously recognized, but can explain the sloping continuum observed in Adirondack-class rock spectra as well as the apparent distortion of an olivine absorption. Spectral mixing is not completely linear, leading to the overestimation of sulfate and olivine fractions and the underestimation of plagioclase feldspar, although linear mixing appears to successfully replicate the majority of the observed signal. Published TES spectra of low albedo, low dust cover, olivine-bearing materials do not exhibit the spectral telltales of non-linear behavior, probably because orbital spectra represent mostly mobile regolith that has not accumulated a sufficient dust cover over ～3 × 6 km areas.  相似文献   

13.
E.Z. Noe Dobrea  F. Poulet 《Icarus》2008,193(2):516-534
We have identified the presence of polyhydrated sulfates in association with crystalline gray hematite in outcrop units of the chaotic terrain east of Valles Marineris. The hematite is found in abundances of up to ∼18%, and is usually associated with thin (∼10's of meters) cliff-forming layers of intermediate-toned outcrops (albedo ∼0.15-0.20) as well as mantling deposits adjacent to the outcrops. The polyhydrated sulfates are usually restricted to the bedrock unit, and are not found in the adjacent mantling units. In analogy to the observations performed at the Opportunity landing site, we hypothesize that erosion of the sulfate/hematite-bearing outcrops leaves the hematite behind as a lag and breaks the sulfates down to wind-transportable sizes. We also find that the layered outcrops present, for the most part, embayment or on-lap relationships with respect to the hummocks that constitute the chaotic terrain, suggesting that these units were emplaced via subaqueous or aeolian deposition and/or flow after the event that formed the associated chaos. These morphological observations, in conjunction with the correlation between hematite and polyhydrated sulfates also suggest an aqueous genesis for the crystalline gray hematite in these chaotic units, and presents evidence for the action of aqueous processes after the formation of at least some of the chaotic units on Mars.  相似文献   

14.
Driss Takir  Joshua P. Emery 《Icarus》2012,219(2):641-654
This paper examines the distribution and the abundance of hydrated minerals (any mineral that contains H2O or OH) on outer Main Belt asteroids spanning the 2.5 < a < 4.0 AU region. The hypothesis we are testing is whether planetesimals that accreted closer to the Sun experienced a higher degree of aqueous alteration. We would expect then to see a gradual decline of the abundance of hydrated minerals among the outer Main Belt asteroids with increasing heliocentric distance (2.5 < a < 4.0 AU). We measured spectra (0.8–2.5 μm and 1.9–4.1 μm) of 28 outer Main Belt asteroids using the SpeX spectrograph/imager at the NASA Infrared Telescope Facility (IRTF). We identified four groups on the basis of the shape and the band center of the 3-μm feature. The first group, which we call “sharp”, exhibits a sharp 3-μm feature, attributed to hydrated minerals (phyllosilicates). Most asteroids in this group are located in the 2.5 < a < 3.3 AU region. The second group, which we call “Ceres-like”, consists of 10 Hygiea and 324 Bamberga. Like Asteroid Ceres, these asteroids exhibit a 3-μm feature with a band center of 3.05 ± 0.01 μm that is superimposed on a broader absorption feature from ～2.8 to 3.7 μm. The third group, which we call “Europa-like”, includes 52 Europa, 31 Euphrosyne, and 451 Patientia. Objects in this group exhibit a 3-μm feature with a band center of 3.15 ± 0.01 μm. Both the Ceres-like and Europa-like groups are concentrated in the 2.5 < a < 3.3 AU region. The fourth group, which we call “rounded”, is concentrated in the 3.4 < a < 4.0 AU region. Asteroids in this group are characterized by a rounded 3-μm feature, attributed to H2O ice. A similar rounded 3-μm feature was also identified in 24 Themis and 65 Cybele. Unlike the sharp group, the rounded group did not experience aqueous alteration. Of the asteroids observed in this study, 140 Siwa, a P-type, is the only one that does not exhibit a 3-μm feature. These results are important to constrain the nature and the degree of aqueous alteration in outer Main Belt asteroids.  相似文献   

15.
In the history of Mars exploration its atmosphere and planetary climatology aroused particular interest. In the study of the minor gases abundance in the Martian atmosphere, water vapour became especially important, both because it is the most variable trace gas, and because it is involved in several processes characterizing the planetary atmosphere. The water vapour photolysis regulates the Martian atmosphere photochemistry, and so it is strictly related to carbon monoxide. The CO study is very important for the so-called “atmosphere stability problem”, solved by the theoretical modelling involving photochemical reactions in which the H2O and the CO gases are main characters.The Planetary Fourier Spectrometer (PFS) on board the ESA Mars Express (MEX) mission can probe the Mars atmosphere in the infrared spectral range between 200 and 2000 cm?1 (5–50 μm) with the Long Wavelength Channel (LWC) and between 1700 and 8000 cm?1 (1.2–5.8 μm) with the Short Wavelength Channel (SWC). Although there are several H2O and CO absorption bands in the spectral range covered by PFS, we used the 3845 cm?1 (2.6 μm) and the 4235 cm?1 (2.36 μm) bands for the analysis of water vapour and carbon monoxide, respectively, because these ranges are less affected by instrumental problems than the other ones. The gaseous concentrations are retrieved by using an algorithm developed for this purpose.The PFS/SW dataset used in this work covers more than two and a half Martian years from Ls=62° of MY 27 (orbit 634) to Ls=203° of MY 29 (orbit 6537). We measured a mean column density of water vapour of about 9.6 pr. μm and a mean mixing ratio of carbon monoxide of about 990 ppm, but with strong seasonal variations at high latitudes. The seasonal water vapour map reproduces very well the known seasonal water cycle. In the northern summer, water vapour and CO show a good anticorrelation most of the time. This behaviour is due to the carbon dioxide and water sublimation from the north polar ice cap, which dilutes non-condensable species including carbon monoxide. An analogous process takes place during the winter polar cap, but in this case the condensation of carbon dioxide and water vapour causes an increase of the concentration of non-condensable species. Finally, the results show the seasonal variation of the carbon monoxide mixing ratio with the surface pressure.  相似文献   

16.
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   

17.
CRISM indicates the presence of water ice patches in Richardson crater, located on Mars’ southern polar region at the area of the seasonal ice cap. Numerical simulations suggest that the maximum daytime temperature of the ice at these locations is between 195 and 220 K during local spring. Previous studies suggest that at these temperatures liquid interfacial water could be present. Here, for the first time, we provide an example where the environmental conditions allow for the formation of such liquid films on present day Mars at the southern hemisphere. The upper bound estimated H2O loss during the presence of these water ice patches is approximately 30 μm between Ls = 200 and 220, though it may be as low as 0.1 μm depending on the ambient water vapor. The upper bound value is larger than the expected condensation thickness in autumn; however, it may still be realistic due to CO2 gas jet generated deposition and possible subsequent accumulation on mineral grains. The presence of this interfacial water may have impact on local chemical processes along with astrobiological importance.  相似文献   

18.
《Planetary and Space Science》2007,55(13):2025-2036
Titan's vast equatorial fields of RADAR-dark longitudinal dunes seen in Cassini RADAR synthetic aperture images correlate with one of two dark surface units discriminated as “brown” and “blue” in Visible and Infrared Mapping Spectrometer (VIMS) color composites of short-wavelength infrared spectral cubes (RGB as 2.0, 1.6, 1.3 μm). In such composites bluer materials exhibit higher reflectance at 1.3 μm and lower at 1.6 and 2.0 μm. The dark brown unit is highly correlated with the RADAR-dark dunes. The dark brown unit shows less evidence of water ice suggesting that the saltating grains of the dunes are largely composed of hydrocarbons and/or nitriles. In general, the bright units also show less evidence of absorption due to water ice and are inferred to consist of deposits of bright fine precipitating tholin aerosol dust. Some set of chemical/mechanical processes may be converting the bright fine-grained aerosol deposits into the dark saltating hydrocarbon and/or nitrile grains. Alternatively the dark dune materials may be derived from a different type of air aerosol photochemical product than are the bright materials. In our model, both the bright aerosol and dark hydrocarbon dune deposits mantle the VIMS dark blue water ice-rich substrate. We postulate that the bright mantles are effectively invisible (transparent) in RADAR synthetic aperture radar (SAR) images leading to lack of correlation in the RADAR images with optically bright mantling units. RADAR images mostly show only dark dunes and the water ice substrate that varies in roughness, fracturing, and porosity. If the rate of deposition of bright aerosol is 0.001–0.01 μm/yr, the surface would be coated (to optical instruments) in hundreds-to-thousands of years unless cleansing processes are active. The dark dunes must be mobile on this very short timescale to prevent the accumulation of bright coatings. Huygens landed in a region of the VIMS bright and dark blue materials and about 30 km south of the nearest occurrence of dunes visible in the RADAR SAR images. Fluvial/pluvial processes, every few centuries or millennia, must be cleansing the dark floors of the incised channels and scouring the dark plains at the Huygens landing site both imaged by Descent Imager/Spectral Radiometer (DISR).  相似文献   

19.
The equilibrium suggested as a buffer for CO2 in the Venus atmosphere, CaCO3 + SiO2 = CaSiO3 + CO2, cannot act as a buffer at the Venus surface/troposphere – the pressure–temperature slope of the equilibrium and that of the atmosphere (dry adiabat with significant greenhouse heating) do not provide buffering capacity (if indeed CaCO3 were present). Instead, perturbations to T or P(CO2) can produce catastrophic expansion or collapse of the atmosphere. This instability can be generalized to all devolatilization reactions that produce a radiatively active gas in a planetary atmosphere dominated by such gases, and gives a simple thermochemical criterion for whether a reaction could buffer such an atmosphere. Simple decarbonation reactions fail this criterion, suggesting that the abundance of CO2 in a CO2-dominated atmosphere cannot be buffered by chemical reactions with the surface; a similar conclusion holds for the abundance of H2O in an H2O-dominated (steam) atmosphere. Buffering of minor gases is more likely; a mineral buffer equilibrium for SO2 proposed for Venus, FeS2 + CO2 = Fe3O4 + SO2 + CO, passes the thermochemical criterion, as does a reaction involving Ca sulfate. These inferences can be generalized to atmospheres in ‘moist’ adiabatic equilibria, and to extrasolar Venus-like planets, and will help in interpreting the compositions of their atmospheres.  相似文献   

20.
This work is a continuation of our previous paper about brightening of Comet 17P/Holmes (Kossacki, K.J., Szutowicz, S. [2010]. Icarus 207, 320–340). In that paper we presented results of simulations indicating that the nonuniform crystallization of amorphous water ice itself is probably not sufficient for an explosion. In the present work we investigate the possibility that the explosion is caused by a rapid sublimation of the CO ice leading to the rise of gas pressure above the tensile strength of the nucleus. We simulated evolution of a model nucleus in the orbit of Comet 17P/Holmes. The nucleus is composed of water ice, carbon monoxide ice and dust and has the shape of an elongated ellipsoid. The simulations include crystallization of amorphous ice in the nucleus, changes of the dust mantle thickness, and sublimation of the CO ice. In our model CO is mantling grains composed of dust and amorphous water ice. Orientation of the nuclear spin axis in space is the same as derived in Moreno et al. (Moreno, F., Ortiz, J.L., Santos-Sanz, P., Morales, N., Vidal-Nunez, M.J., Lara, L.M., Gutierrez, P.J. [2008]. Astrophys. J. 677, L63–L66) for Comet Holmes during recent brightening event. Hence, the angle between the orbital and the equatorial planes of the comet is I = 95°, and the cometocentric solar longitude at perihelion is Φ = 210°. The calculations are performed for the south pole being the sub-solar point close to time of the outburst. Our computations indicate, that the CO pressure within the comet nucleus can rise to high values. When the layer between the dust mantle and the crystallization front of the amorphous water ice is very fine grained, few microns in radius, the CO pressure within the nucleus can exceed 10 kPa. This value is the lowest estimate for the tensile strength of the nucleus of Comet Holmes (Reach, W.T., Vaubaillon, J., Lisse, C.M., Holloway, M., Rho, J. [2010]. Icarus 208, 276–292). Hence, when the gas pressure reaches this value the nucleus may explode.  相似文献   

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