共查询到20条相似文献，搜索用时 15 毫秒
1.
Near-infrared spectra of the near-Earth object (100085) 1992 UY4 are similar to those of P-type asteroids, providing a fitted geometric albedo of 0.052±0.005 and an effective diameter of 1.68±0.08 km. This object, with a likely outer-belt origin, also exhibits a 3-μm absorption feature with a band depth of 3%±1%, corresponding to a regolithic bulk hydrogen-to-silicon ratio of 0.30±0.05. The bulk of this hydrogen seems to be present in H2O-dominated minerals. 相似文献
2.
Roger N. Clark 《Icarus》1980,44(2):388-409
The reflectance spectra of Ganymede, Europa, Callisto, and Saturn's rings are analyzed using recent laboratory reflectance studies of water frost, water ice, and water and mineral mixtures. It is found that the spectra of the icy Galilean satellites are characteristic of water ice (e.g., ice blocks or possibly very large ice crystals ? 1 cm) or frost on ice rather than pure water frost, and that the decrease in reflectance at visible wavelengths is caused by other mineral grains in the surface. The spectra of Saturn's rings are more characteristic of water frost with some other mineral grains mixed in the frost but not on the surface. The impurities on all these objects are not in spectrally isolated patches but appear to be intimately mixed with the water. The impurity grains appear to have reflectance spectra typical of minerals containing Fe3+. Some carbonaceous chondrite meteorite spectra show the necessary spectral shape. Ganymede is found to have more water ice on the surface than previously thought (～90 wt%), as is Callisto (30–90 wt%). The surface of Europa has a vast frozen water surface with only a few percent impurities. Saturn's rings also have only a few percent impurities. The amount of bound water or bound OH for these objects is 5 ± 5 wt% averaged over the entire surface. Thus with the small amount of nonicy material present on these objects, no hydrated minerals can be ruled out. A new absorption feature is identified in Ganymede, Callisto, and probably Europa at 1.5 μm which is also seen in the spectra of Io but not in Saturn's rings. This feature has not been seen in laboratory studies and its cause is unknown. 相似文献
3.
The visible to near-infrared spectral reflectance properties of intimate and areal pyroxene?+?palagonitic material mixtures as well as pure mafic silicates (low-calcium pyroxene, high-calcium pyroxene, pigeonite, olivine) and mixtures of these minerals were analyzed at high spectral resolution (5 nm) as well as with non-contiguous band passes equivalent to recent HST observations and the Pathfinder IMP in order to determine the quality and quantity of mineralogical information (end member compositions, abundances, and grain sizes) derivable in the presence of palagonitic material. In the case of pyroxene?+?palagonitic material mixtures, pyroxene is detectable at abundances as low as 10 wt%, and its composition can be constrained because (a) its diagnostic absorption feature (located near 1000 nm) persists even for high palagonitic material abundances, and (b) palagonitic material does not appreciably alter the wavelength position of this band (<4 nm variation). For broad band data (such as Pathfinder IMP band passes), different mafic silicates can be discriminated and palagonitic material abundances constrained using a variety of reflectance ratios and three-point “absorption band depths.” However, other properties of mafic silicate?±?palagonitic material assemblages, such as mafic silicate major element compositions, grain sizes, and end member abundances, generally cannot be rigorously quantified. The use of multiple reflectance ratios can, however, be used to identify relative changes in these properties, as most changes in mafic silicate?±?palagonitic material assemblage properties are characterized by a unique corresponding set of reflectance ratio variations. The observed spectral-assemblage property trends are consistent with those expected from the known spectral properties of the end members. 相似文献
4.
Visible-near infrared reflectance spectra for five particle size fractions of a Hawaiian palagonite (HWMK101) and a nontronite (ferruginous smectite, Clay Minerals Society source clay SWa-1) were measured under ambient, purged, and heated conditions to characterize the effects of surface and volume scattering on the relationship between absolute H2O content and the strength of the 3 μm absorption feature. Both materials were ground and dry sieved to particle sizes of <25, 25-45, 45-75, 75-125, and 125-250 μm. Particles of the bulk palagonite have an approximate bimodal distribution consisting of small, amorphous particles <5 μm in diameter mixed with crystalline and glass particles <1 mm in diameter, whereas the nontronite particles are polycrystalline aggregates. We find that band parameters value relating the strength of the 3 μm hydration feature to water content increase with particle size for a given water content, regardless of whether reflectance or single scattering albedo spectra are used. Spectra generally increase in reflectance as particle size decreases, a result of the relative increase in volume to surface scattering. Spectra of large particles are commonly saturated in the 3 μm region due to an increase in optical path length, making an accurate estimate of water content indeterminate until the samples dehydrate to the volume-scattering regime. We find that the presence of fines in several of the size fractions of palagonite cause their spectra to be representative of the finest fraction rather than the mean particle size. The nontronite spectra appear to be representative of an effective particle size within the range of the sieved size fractions. Many planetary surfaces are expected to have a large number of small particles which can dominate their spectral signature. Our results for particles <45 μm provide a reasonable model for estimating the H2O content of hydrated asteroids and regions of Mars. 相似文献
5.
New image-tube spectra of Triton are analyzed for a determination of the reflectance of the satellite between 0.32 and 0.74 μm. Comparison of the violet reflectance of Triton with that of terrestrial minerals, lunar samples, and meteorites, gives evidence that the satellite surface is composed largely of rocky material having the same sources of violet opacity (mineral charge transfer and crystal field transitions). New radiometric observations set a stringent upper limit to the satellite radius (r ? 2600 km) and a lower limit to the geometric albedo (pv ? 0.19). The albedo can be somewhat higher and still within the range allowed by a rocky surface. No useful constraints can be put on the mean density of Triton because of remaining uncertainties in the radius and the mass. The image-tube spectra show no evidence of gaseous absorption in the methane bands, though a stronger band has been found in the infrared at 2.3 μm (Cruikshank and Silvaggio, 1979, in press; the near-infrared photometric colors may be affected by the CH4 band. Rayleigh scattering computations of a potential inert atmospheric component of Triton appear to preclude the presence of large quantities of nitrogen and the noble gases. 相似文献
6.
The mineralogy of Mars is well understood on a qualitative level at a global scale due to satellite data. Quantitative analysis of visible and near-infrared (VNIR) satellite data is a desirable but nontrivial task, due partly to the nonlinearity of VNIR reflectance spectra from the mineral mixtures of the Martian surface. In this study, we investigated the use of the Hapke radiative transfer model to generate linearly mixed single scattering albedo data from nonlinearly mixed VNIR reflectance data and then quantitatively analyzed them using the linear spectral mixture model. Simplifications to the Hapke equation were tested accounting for variables that would be unknown when using satellite data. Mineral mixture spectra from the RELAB spectral library were degraded to test the robustness of the unmixing technique in the face of data that mimic some of the complexities of satellite spectral data collected at Mars. A final test was performed on spectra from shergottite meteorites to assess the technique against real Martian mineral mixtures. The simplified Hapke routine produced robust abundance estimates within 5–10% accuracy when applied to laboratory standard spectra from the synthetic mixtures of igneous minerals in agreement with previous studies. The results of tests involving degraded data to mimic the low spectral contrast of the Martian surface and the lack of a priori knowledge of the constituent mineral spectral endmembers, however, were less encouraging, with errors in abundance estimation greater than 25%. These results cast doubt on the utility of Hapke unmixing for the quantitative analysis of VNIR data of the surface of Mars. 相似文献
7.
Storage of hydrogen atoms in or on a planetary surface can take place via several different mechanisms. If the hydrogen atom reacts to form a hydroxyl (OH) group or water molecule, an absorption band near 3 μm will be present. Many possible mechanisms for sequestering atomic hydrogen are discussed: internal hydrogen in the form of non-structural OH and H2O in nominally-anhydrous minerals, structural OH in minerals, structural H2O in minerals, H2O in fluid inclusions, and OH and H2O in glasses; bulk H2O as either liquid water or ice; and surficial hydrogen that is either physisorbed as H2O, chemisorbed as an H2O surface complex, or chemically-bound as an OH group on surface terminal sites and grain boundary regions. Understanding the spectroscopic distinctions among these various phenomena is of critical importance in constraining both the evolution of planetary interiors and the cycling of water on planetary surfaces. Proper interpretation of 3-μm bands in reflectance spectra is shown to depend upon the relative contributions from surficial vs. interior hydrogen, which vary with effective surface area (i.e., the grain size and surface roughness) and the volume sampled by the spectrometer. 相似文献
8.
9.
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
10.
G. Hansen M. Giuranna S. Fonti H. Hirsh A. Maturilli G. Piccioni B. Saggin 《Planetary and Space Science》2005,53(10):1089-1095
The Mars Express spacecraft has a highly inclined orbit around Mars and so has been able to observe the south pole of Mars in illuminated conditions at the end of the southern summer (Ls=330). Spectra from the planetary Fourier spectrometer (PFS) short wavelength (SW) channel were recorded over the permanent ice cap to study its composition in terms of CO2 ice and H2O ice. Models are fitted to the observed data, which include a spatial mixture of soil (not covered by ice) and CO2 frost (with a specific grain size and a small amount of included dust and H2O ice). Two different kinds of spectra were observed: those over the permanent polar cap with almost pure CO2 ice, negligible water ice, no soil fraction required, and bright; and those over mixed terrain (at the edge of the cap or near troughs) containing a significant soil spatial fraction, more water ice and smaller CO2 grain size. The amount of water ice given by fits to scaled albedo models is less than 10 ppm by weight. When using multi-stream reflectance models with the appropriate lighting geometry, the water amount must be 2-5 times greater than the albedo fit (less than 50 ppm). At the periphery of the residual polar cap, we found a region almost completely covered by water frost, modeled as a mixture of micron-sized and sub-mm sized grains. Our result using a granular mixture of micron-sized grains of water ice and dust with the CO2 grains is different from the modeling of OMEGA polar cap observations using molecular mixtures. 相似文献
11.
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
12.
Mariner 10 clear filter (490 nm) images of Mercury were recalibrated and photometrically normalized to produce a mosaic of nearly an entire hemisphere of the planet. Albedo contrasts are slightly larger than seen in the lunar highlands (excluding maria). Variegations indicative of compositional differences include diffuse low albedo units often overlain by smooth plains, the high albedo smooth plains of Borealis Planitia, and high-albedo enigmatic crater floor deposits. A higher level of contrast between immature crater ejecta and average mature material on Mercury compared to the Moon is consistent with a more intense space weathering environment on Mercury that results in a more mature regolith. Immature lunar highlands materials are ∼1.5 times higher in reflectance than analogous immature mercurian materials. Immature materials of the same composition would have the same reflectance on both bodies, thus this observation requires that Mercury's crust contains a significant darkening agent, either opaque minerals or ferrous iron bearing silicates, in abundances significantly higher than those of the lunar highlands. If the darkening agent is opaque minerals (e.g. ilmenite or ulvospinel) Mercury's crust may contain significant ferrous iron and yet not exhibit a 1-μm absorption band. 相似文献
13.
T.B. McCord G.B. Hansen B.J. Buratti R.N. Clark D.P. Cruikshank E. D&#x;Aversa C.A. Griffith E.K.H. Baines R.H. Brown C.M. Dalle Ore G. Filacchione V. Formisano C.A. Hibbitts R. Jaumann J.I. Lunine R.M. Nelson C. Sotin the Cassini VIMS Team 《Planetary and Space Science》2006,54(15):1524-1539
Titan's bulk density along with Solar System formation models indicates considerable water as well as silicates as its major constituents. This satellite's dense atmosphere of nitrogen with methane is unique. Deposits or even oceans of organic compounds have been suggested to exist on Titan's solid surface due to UV-induced photochemistry in the atmosphere. Thus, the composition of the surface is a major piece of evidence needed to determine Titan's history. However, studies of the surface are hindered by the thick, absorbing, hazy and in some places cloudy atmosphere. Ground-based telescope investigations of the integral disk of Titan attempted to observe the surface albedo in spectral windows between methane absorptions by calculating and removing the haze effects. Their results were reported to be consistent with water ice on the surface that is contaminated with a small amount of dark material, perhaps organic material like tholin. We analyze here the recent Cassini Mission's visual and infrared mapping spectrometer (VIMS) observations that resolve regions on Titan. VIMS is able to see surface features and shows that there are spectral and therefore likely compositional units. By several methods, spectral albedo estimates within methane absorption windows between 0.75 and 5 μm were obtained for different surface units using VIMS image cubes from the Cassini-Huygens Titan Ta encounter. Of the spots studied, there appears to be two compositional classes present that are associated with the lower albedo and the higher albedo materials, with some variety among the brighter regions. These were compared with spectra of several different candidate materials. Our results show that the spectrum of water ice contaminated with a darker material matches the reflectance of the lower albedo Titan regions if the spectral slope from 2.71 to 2.79 μm in the poorly understood 2.8-μm methane window is ignored. The spectra for brighter regions are not matched by the spectrum of water ice or unoxidized tholin, in pure form or in mixtures with sufficient ice or tholin present to allow the water ice or tholin spectral features to be discerned. We find that the 2.8-μm methane absorption window is complex and seems to consist of two weak subwindows at 2.7 and 2.8 μm that have unknown opacities. A ratio image at these two wavelengths reveals an anomalous region on Titan that has a reflectance unlike any material so far identified, but it is unclear how much the reflectances in these two subwindows pertain to the surface. 相似文献
14.
Spectral detectability of Ca- and Mg-sulfates in Martian bright soils in the 4–5 μm wavelength range
《Planetary and Space Science》2007,55(4):429-440
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
15.
The near-Earth object (99942) Apophis will make an extremely close approach to the Earth in 2029, and currently has approximately a one-in-45,000 chance of impacting our planet in 2036 (JPL Sentry, November 2006). Computation of the orbital evolution of this object is limited by insufficient knowledge of physical properties required to determine the role played by non-gravitational effects. Using polarimetric observations, we have obtained the first reliable determination of the albedo of Apophis, obtaining 0.33±0.08. We also derive an updated estimate of the asteroid's absolute magnitude: H=19.7±0.4. Using this albedo and H, we find that Apophis has a diameter of 270±60 m, slightly smaller than preliminary estimates based upon an assumed albedo. Our observations demonstrate the feasibility of polarimetric observations aimed at obtaining albedos and sizes of small, potentially hazardous asteroids. 相似文献
16.
Edward A. Cloutis Kaitlyn A. McCormack Amanda R. Hendrix Michael A. Craig Stanley A. Mertzman Miriam A. Riner 《Icarus》2008,197(1):321-347
Ultraviolet spectral reflectance properties (200-400 nm) of a large number of minerals known or presumed to exist on the surfaces of Mars, the Moon, and asteroids, and in many meteorites, were investigated. Ultraviolet reflectance spectra (200-400 nm) of these minerals range from slightly blue-sloped (reflectance decreasing toward longer wavelengths) to strongly red-sloped (reflectance increasing toward longer wavelengths). Most exhibit one or two absorption features that are attributable to FeO charge transfers involving Fe3+ or Fe2+. The UV region is a very sensitive indicator of the presence of even trace amounts (<0.01 wt%) of Fe3+ and Fe2+. The major Fe3+O absorption band occurs at shorter wavelengths (∼210-230 nm), and is more intense than the major Fe2+O absorption band (∼250-270 nm). Ti-bearing minerals, such as ilmenite, rutile and anatase exhibit UV absorption bands attributable to Ti4+O charge transfers. While the positions of metal-O charge transfer bands sometimes differ for different minerals, the variation is often not diagnostic enough to permit unique mineral identification. However, iron oxides and oxyhydroxides can generally be distinguished from Fe-bearing silicates in the 200-400 nm region on the basis of absorption band positions. Within a given mineral group (e.g., low-calcium pyroxene, olivine, plagioclase feldspar), changes in Fe2+ or Fe3+ abundance do not appear to result in a measurable change in absorption band minima positions. Absorption band positions can vary as a function of grain size, however, and this variation is likely due to band saturation effects. The intensity of metal-O charge transfers means that some minerals will exhibit saturated UV absorption bands even for fine-grained (<45 μm) powders. In cases where absorption bands are not saturated (e.g., Fe2+O bands in some plagioclase feldspars and pyroxenes), changes in Fe2+ content do not appear to cause variations in band position. In other minerals (e.g., olivine), changes in band positions are correlated with compositional and/or grain size variations, but this is likely due to increasing band saturation rather than compositional variations. Overall, we find that the UV spectral region is sensitive to different mineral properties than longer wavelength regions, and thus offers the potential to provide complementary capabilities and unique opportunities for planetary remote sensing. 相似文献
17.
B.J. Buratti K. Soderlund J.A. Mosher D.P. Simonelli R.N. Clark D.P. Cruikshank 《Icarus》2008,193(2):309-322
Three weeks prior to the commencement of Cassini's 4 year tour of the saturnian system, the spacecraft executed a close flyby of the outer satellite Phoebe. The infrared channel of the Visual Infrared Mapping Spectrometer (VIMS) obtained images of reflected light over the 0.83-5.1 μm spectral range with an average spectral resolution of 16.5 nm, spatial resolution up to 2 km, and over a range of solar phase angles not observed before. These images have been analyzed to derive fundamental photometric parameters including the phase curve and phase integral, spectral geometric albedo, bolometric Bond albedo, and the single scattering albedo. Physical properties of the surface, including macroscopic roughness and the single particle phase function, have also been characterized. Maps of normal reflectance show the existence of two major albedo regimes in the infrared, with gradations between the two regimes and much terrain with substantially higher albedos. The phase integral of Phoebe is 0.29±0.03, with no significant wavelength dependence. The bolometric Bond albedo is 0.023±007. We find that the surface of Phoebe is rough, with a mean slope angle of 33°. The satellite's surface has a substantial forward scattering component, suggesting that its surface is dusty, perhaps from a history of outgassing. The spectrum of Phoebe is best matched by a composition including water ice, amorphous carbon, iron-bearing minerals, carbon dioxide, and Triton tholin. The characteristics of Phoebe suggest that it originated outside the saturnian system, perhaps in the Kuiper Belt, and was captured on its journey inward, as suggested by Johnson and Lunine (2005). 相似文献
18.
A new infrared spectrum of the leading side of Rhea is presented in the 0.65- to 2.5 μm region with 1.5% spectral resolution and 3 to 5% data precision. Water ice absorptions previously identified at 2.02, 1.65, and 1.55 μm are confirmed and more precisely defined. The 1.25-μm water ice absorption is identified for the first time and the 1.04-μm water ice absorption is probably also present. The spectrum of the leading side of Rhea is very similar to the spectrum of the leading side of Ganymede in the 0.6- to 2.5-μm region. The Rhea spectrum is also very similar to laboratory spectra of water frost on ice blocks rather than that of an optically thick frost. The strong water ice absorption features, high albedo, and little downturn in reflectance toward shorter wavelengths from 0.6 to 0.4 μm all indicate a surface of nearly pure water ice. The surface of Rhea is probably at least 90 wt% water ice and may be as much as 98 wt%. Of the remaining constituents, neither minerals nor clathrathes can be excluded. If the surface of Rhea were a methane clathrate, the surface would still be about 90 wt% water ice. 相似文献
19.
We present thermal emission spectra (5.2-38 μm) of the Trojan asteroids 624 Hektor, 911 Agamemnon, and 1172 Aneas. The observations used the Infrared Spectrograph (IRS) on board the Spitzer Space Telescope. Emissivity spectra are created by dividing the measured Spectral Energy Distribution (SED) by a model of the thermal continuum. We employ the Standard Thermal Model (STM), allowing physical parameters (e.g., radius and albedo) to vary in order to find the best thermal continuum fit to the SED. The best-fit effective radius (R) and visible geometric albedo (pv) for Hektor (R=110.0±7.3, ) and Aneas (R=69.1±5.1, ) agree very well with previous estimates, and for Agamemnon (R=71.5±5.2, ) we find slightly a smaller size and higher albedo than previously derived. Other thermal models (e.g., thermophysical) result in estimates of R and pv that vary a few percent from the STM, but the resulting emissivity spectra are identical. The emissivity spectra of all three asteroids display an emissivity plateau near 10-μm and another broader rise from ∼18 to 28 μm. We interpret these as indications of fine-grained silicates on the surfaces of these asteroids. The emissivity spectra more closely resemble emission spectra from cometary comae than those from solid surfaces and measured in the laboratory for powdered meteorites and regolith analogs. We hypothesize that the coma-like emission from the solid surfaces of trojans may be due to small silicate grains being imbedded in a relatively transparent matrix, or to a very under-dense (fairy-castle) surface structure. These hypotheses need to be tested by further laboratory and theoretical scattering work as well as continued thermal emission observations of asteroids. 相似文献
20.
F. Poulet N. Mangold J.-M. Bardintzeff V. Sautter J.-P. Bibring Y. Langevin A. Aléon-Toppani 《Icarus》2009,201(1):84-243
The primary objectives of this paper are to determine the modal mineralogy of selected low albedo terrains of different ages ranging from Noachian to Amazonian exposed on the surface of Mars. This analysis is conducted using the spectral modeling of the Observatoire pour la Minéralogie, l'Eau, les Glaces, et l'Activité (OMEGA) reflectance data. Results from this work are consistent with the major results of previous spectroscopic studies: plagioclase (40-60% in volume) and high calcium pyroxene (20-40%, HCP) are the dominant minerals of the most regions. Low calcium pyroxene (10-15%, LCP) and minor amounts of olivine are also present. The oldest terrains are characterized by the largest amount of LCP and the lowest concentration of plagioclase. These overall compositions are consistent with two-pyroxene basalts. The particle sizes are in the range of a few hundreds of micrometers, which is in good agreement with the thermal inertia of the martian low albedo regions. In the region around the Nili Fossae, localized concentrations of olivine up to 40% with millimeter particle size similar to picritic basalts observed in situ by the Spirit rover in the Gusev crater are inferred. Chemical compositions are calculated for the first time from OMEGA spectra. They are quite consistent with Gusev rocks and shergottite compositions but they appear to be significantly SiO2-poorer than Thermal Emission Spectrometer data. A decreasing low calcium pyroxene abundance with the decreasing age of the low albedo regions is reported. This may be indicative of decreasing degree of partial melting as thermal flux decreases with time. We propose that the ancient Noachian-aged, LCP-rich terrains could have been formed from H2O-bearing melts. Then, dry, basaltic volcanism occurred leading to decreasing LCP abundance with time due to decreasing degree of partial melting. The olivine-bearing material modeled in Nili Fossae resembles the composition of ALH77005 and Chassigny meteorites consistent with prior studies. Implications on the formation of the basaltic Shergottites are discussed. 相似文献