Absorption bands near three micrometers in diffuse reflectance spectra of carbonaceous chondrites: Comparison with asteroids

Abstract— We measured infrared diffuse reflectance spectra of several carbonaceous chondrites in order to obtain additional information on the surface materials of their presumed parent bodies, C-type asteroids. The presence and intensity of absorption bands near 3 μm in the reflectance spectra are due to the presence and abundance of hydrates and/or hydroxyl ions. The absorption features of the 3 μm hydration bands of carbonaceous chondrites were compared with those of asteroids 1 Ceres and 2 Pallas. They are commonly classified into separate subtypes, G- and B-type. The spectral shapes of Pallas and Renazzo (CR2 chondrite) around the 3 μm absorption band are an excellent match. This result may suggest that the amount of hydrous minerals in the surface material of Pallas is smaller than that in the CM2 or CI chondrites, and the hydrous minerals on the surface of Pallas may be similar to those found in Renazzo. The spectral features around the 3 μm band of Ceres are different from those of carbonaceous chondrites studied in this paper.     

Characteristic features in the spectra of Europa, Ganymede, and Callisto

The results of ground-based spectrophotometry of the icy Galilean satellites of Jupiter—Europa, Ganymede, and Callisto—are discussed. The observations were carried out in the 0.39–0.92 μm range with the use of the CCD spectrometer mounted on the 1.25-m telescope of the Crimean laboratory of the Sternberg Astronomical Institute in March 2004. It is noted that the calculated reflectance spectra of the satellites mainly agree with the analogous data of the earlier ground-based observations and investigations in the Voyager and Galileo space missions. The present study was aimed at identifying new weak absorption bands (with the relative intensity of ～3–5%) in the reflectance spectra of these bodies with laboratory measurements (Landau et al., 1962; Ramaprasad et al., 1978; Burns, 1993; Busarev et al., 2008). It has been ascertained that the spectra of all of the considered objects contain weak absorption bands of molecular oxygen adsorbed into water ice, which is apparently caused by the radiative implantation of O⁺ ions into the surface material of the satellites in the magnetosphere of Jupiter. At the same time, spectral features of iron of different valence (Fe²⁺ and Fe³⁺) values typical of hydrated silicates were detected on Ganymede and Callisto, while probable indications of methane of presumably endogenous origin, adsorbed into water ice, were found on Europa. The reflectance spectra of the icy Galilean satellites were compared to the reflectance spectra of the asteroids 51 Nemausa (C-class) and 92 Undina (X-class).     

Spectral reflectance properties of carbonaceous chondrites: 2. CM chondrites

We have examined the spectral reflectance properties and available modal mineralogies of 39 CM carbonaceous chondrites to determine their range of spectral variability and to diagnose their spectral features. We have also reviewed the published literature on CM mineralogy and subclassification, surveyed the published spectral literature and added new measurements of CM chondrites and relevant end members and mineral mixtures, and measured 11 parameters and searched pair-wise for correlations between all quantities. CM spectra are characterized by overall slopes that can range from modestly blue-sloped to red-sloped, with brighter spectra being generally more red-sloped. Spectral slopes, as measured by the 2.4:0.56 μm and 2.4 μm:visible region peak reflectance ratios, range from 0.90 to 2.32, and 0.81 to 2.24, respectively, with values <1 indicating blue-sloped spectra. Matrix-enriched CM spectra can be even more blue-sloped than bulk samples, with ratios as low as 0.85. There is no apparent correlation between spectral slope and grain size for CM chondrite spectra - both fine-grained powders and chips can exhibit blue-sloped spectra. Maximum reflectance across the 0.3-2.5 μm interval ranges from 2.9% to 20.0%, and from 2.8% to 14.0% at 0.56 μm. Matrix-enriched CM spectra can be darker than bulk samples, with maximum reflectance as low as 2.1%. CM spectra exhibit nearly ubiquitous absorption bands near 0.7, 0.9, and 1.1 μm, with depths up to 12%, and, less commonly, absorption bands in other wavelength regions (e.g., 0.4-0.5, 0.65, 2.2 μm). The depths of the 0.7, 0.9, and 1.1 μm absorption features vary largely in tandem, suggesting a single cause, specifically serpentine-group phyllosilicates. The generally high Fe content, high phyllosilicate abundance relative to mafic silicates, and dual Fe valence state in CM phyllosilicates, all suggest that the phyllosilicates will exhibit strong absorption bands in the 0.7 μm region (due to Fe³⁺-Fe²⁺ charge transfers), and the 0.9-1.2 μm region (due to Fe²⁺ crystal field transitions), and generally dominate over mafic silicates. CM petrologic subtypes exhibit a positive correlation between degree of aqueous alteration and depth of the 0.7 μm absorption band. This is consistent with the decrease in fine-grained opaques that accompanies aqueous alteration. There is no consistent relationship between degree of aqueous alteration and evidence for a 0.65 μm region saponite-group phyllosilicate absorption band. Spectra of different subsamples of a single CM can show large variations in absolute reflectance and overall slope. This is probably due to petrologic variations that likely exist within a single CM chondrite, as duplicate spectra for a single subsample show much less spectral variability. When the full suite of available CM spectra is considered, few clear spectral-compositional trends emerge. This indicates that multiple compositional and physical factors affect absolute reflectance, absorption band depths, and absorption band wavelength positions. Asteroids with reflectance spectra that exhibit absorption features consistent with CM spectra (i.e., absorption bands near 0.7 and 0.9 μm) include members from multiple taxonomic groups. This suggests that on CM parent bodies, aqueous alteration resulted in the consistent production of serpentine-group phyllosilicates, however resulting absolute reflectances and spectral shapes seen in CM reflectance spectra are highly variable, accounting for the presence of phyllosilicate features in reflectance spectra of asteroids across diverse taxonomic groups.     

Aqueous alteration affecting the irregular outer planets satellites: Evidence from spectral reflectance

The surface reflectance properties of the irregular outer planets satellites are probed for evidence for the presence of aqueous alteration products on their surfaces using the strong correlation between the 3.0-μm water of hydration absorption feature and the 0.7-μm Fe²⁺ → Fe³⁺ oxidized iron feature seen in low-albedo asteroid reflectances, in an effort to expand our understanding of the composition of the precursor bodies from which the dynamical satellite clusters are derived. Equations converting Johnson V and Kron-Cousins RI photometry to Eight Color Asteroid Survey v (0.550 μm), w (0.701 μm), and x (0.853 μm) photometry are derived from relationships defined by Howell (1995, Ph.D. thesis), and coupled with an algorithm previously defined to detect the presence of the 0.7-μm absorption feature in ECAS asteroid photometry [Vilas, F., 1994. Icarus 111, 456-467]. Broadband VRI photometry of Ch-class Asteroid 19 Fortuna acquired during 2004 confirms the efficacy of this method of identifying the presence of the 0.7-μm feature. Photometric observations of many recently discovered irregular outer jovian, saturnian, uranian, and neptunian satellites, coupled with limited asteroid spectroscopy, were examined for the presence of aqueous alteration. The dynamical clusters of outer irregular jovian satellites are mixed between objects that do and do not show this absorption feature. Multiple observations of some objects test both positively and negatively, similar to the surface variegation that has been observed among many C-class asteroids in the main asteroid belt. Evidence for aqueous alteration on these jovian satellites augers for an origin in or near the same location as the asteroids now occupying the aqueous alteration zone (2.6-3.5 AU), at heliocentric distances internal to Jupiter's orbit. Among the saturnian irregular satellites, only S IX Phoebe shows limited evidence of aqueous alteration from ground-based observations. The other satellites show no sign of this feature, and have general reflectance properties very similar to the D-class asteroids, supporting an origin for their precursor bodies in the outer Solar System, perhaps the Centaur region. Only two uranian satellites were tested: U XVII Caliban tests positively for the feature. The differences in surface reflectance properties support the idea that Caliban and U XVI Sycorax derive from separate parent bodies. One observation of neptunian satellite N II Nereid shows no sign of this absorption feature.     

Thermal metamorphism of the C,G, B,and F asteroids seen from the 0.7 μm, 3 μm,and UV absorption strengths in comparison with carbonaceous chondrites

Abstract Thermal metamorphism study of the C, G, B, and F asteroids has been revisited using their UV, visible, NIR, and 3 μm reflectance spectra. High-quality reflectance spectra of seven selected C, G, B, and F asteroids have been compared with spectra for 29 carbonaceous chondrites, including thermally-metamorphosed CI/CM meteorites. There are three sets of spectral counterparts, among which 511 Davida and B-7904 are the most similar to each other in terms of both spectral shape and brightness. By comparing the 0.7 μm and 3 μm absorption strengths of 21 C, G, B, and F asteroids and heated Murchison samples, these asteroids have been grouped into three heating-temperature ranges. These correspond to (1) <400 °C: phyllosilicate-rich; (2) 400–600 °C: phyllosilicates transformed to anhydrous silicates; and (3) >600 °C: fully anhydrous. A good correlation between the UV and 3 μm absorption strengths has been confirmed for the C, G, B, and F asteroids and the CI, CM, and CR meteorites. A plot of the UV absorption strength vs. the IRAS diameter for 142 C, G, B, and F asteroids shows that the maximum UV absorption strength decreases as the diameter increases for the asteroids >60 km, with a notable exception, Ceres. These relationships suggest that some of the larger asteroids may be the heated inner portions of once larger bodies and that common CI/CM meteorites may have come from the lost outer portions, which escaped extensive late-stage heating events.     

Spectral reflectance properties of carbonaceous chondrites: 3. CR chondrites

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.     

Exploration of faint absorption bands in the reflectance spectra of the asteroids by method of optimal smoothing: Vestoids

An optimization method of smoothing noisy spectra was developed to investigate faint absorption bands in the visual spectral region of reflectance spectra of asteroids and the compositional information derived from their analysis. The smoothing algorithm is called “optimal” because the algorithm determines the best running box size to separate weak absorption bands from the noise. The method is tested for its sensitivity to identifying false features in the smoothed spectrum, and its correctness of forecasting real absorption bands was tested with artificial spectra simulating asteroid reflectance spectra. After validating the method we optimally smoothed 22 vestoid spectra from SMASS1 [Xu, Sh., Binzel, R.P., Burbine, T.H., Bus, S.J., 1995. Icarus 115, 1-35]. We show that the resulting bands are not telluric features. Interpretation of the absorption bands in the asteroid spectra was based on the spectral properties of both terrestrial and meteorite pyroxenes. The bands located near 480, 505, 530, and 550 nm we assigned to spin-forbidden crystal field bands of ferrous iron, whereas the bands near 570, 600, and 650 nm are attributed to the crystal field bands of trivalent chromium and/or ferric iron in low-calcium pyroxenes on the asteroids' surface. While not measured by microprobe analysis, Fe³⁺ site occupancy can be measured with Mössbauer spectroscopy, and is seen in trace amounts in pyroxenes. We believe that trace amounts of Fe³⁺ on vestoid surfaces may be due to oxidation from impacts by icy bodies. If that is the case, they should be ubiquitous in the asteroid belt wherever pyroxene absorptions are found. Pyroxene composition of four asteroids of our set is determined from the band position of absorptions at 505 and 1000 nm, implying that there can be orthopyroxenes in all range of ferruginosity on the vestoid surfaces. For the present we cannot unambiguously interpret of the faint absorption bands that are seen in the spectra of 4005 Dyagilev, 4038 Kristina, 4147 Lennon, and 5143 Heracles. Probably there are other spectrally active materials along with pyroxenes on the surfaces of these asteroids.     

Ultraviolet spectral reflectance properties of common planetary minerals

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.     

Infrared diffuse reflectance spectra of carbonaceous chondrites: Amount of hydrous minerals

Abstract— Infrared diffuse reflectance spectra (2.53–25 μm) of some carbonaceous (C) chondrites were measured. The integrated intensity of the absorption bands near 3 μm caused by hydrous minerals were compared with the modal content of hydrous minerals for the meteorites. The CM and CI chondrites show larger values of the integrated intensity than those of the unique C chondrites Y82162, Y86720 and B7904, suggesting that the amount of hydrous minerals in the CM and CI chondrites is larger, which supports the contention that hydrous minerals were dehydrated by thermal metamorphism in the unique chondrites. Orgueil (CI) has the largest value of the integrated intensity among the C chondrites we measured and shows a sharp absorption band at 3685 cm^?1 (2.71 μm) that is not seen in the spectra of the CM chondrites. There is an excellent correlation between the observed hydrogen content in C chondrites and the integrated intensity. The CM chondrites show a wide variation in the strength of absorption bands at 1470 cm^?1 (6.8 μm), despite the similarity in absorption features near 3 μm for all CM chondrites. The 1470 cm^?1 band could be due to the presence of some hydrocarbons but may also be a result of terrestrial alteration processes.     

Could G-class asteroids be the parent bodies of the CM chondrites?

Abstract— I review the dynamical and compositional evidence for possibly linking CM chondrites and asteroids having G-class taxonomic designations. Three G asteroids have been identified through previous theoretical studies as being likely meteorite source bodies due to their locations near resonances. Two of these objects, 19 Fortuna and 13 Egeria, have spectral properties that are consistent with such a linkage with CM chondrites. Fortuna has a similar strength 0.7 μm absorption feature and near-infrared spectral slope to CM chondrites but a weaker ultraviolet feature. Egeria also has the characteristic 0.7 μm feature of CM chondrite spectra but does not match as well in the near-infrared. However, since the 0.7 μm feature is apparent in the spectra of approximately one-half of measured C-type asteroids, no definitive statement about any linkages can be made. Ceres is spectrally different from known meteorites in the 3 μm wavelength region and cannot be convincingly linked with any meteorite group.     

Near-infrared reflectance spectroscopy of Ca-rich clinopyroxenes and prospects for remote spectral characterization of planetary surfaces

We present results of laboratory near-infrared reflectance studies of a set of calcic pyroxenes with comparable calcium contents (Wo_45-50) but variable iron content and oxidation states. This new dataset complements earlier published data (Cloutis and Gaffey, 1991, J. Geophys. Res. 96, 22809-28826, and references therein). In particular, our new spectra extend the scarce available spectral data on chemically analyzed Fe-rich high-Ca clinopyroxenes. We attempted to interpret the spectral behavior of our samples in terms of chemistry and coordination site occupancies. Tentatively, we conclude that Fe-rich calcic pyroxenes have very low contents of Fe²⁺ in the M2 sites and belong to the spectral type A lacking the 2-μm band. This may be due to high Ca and Mn contents in these pyroxenes. Fe-poor high-Ca pyroxenes are more spectrally variable. In general, they tend to belong to the spectral type B with two major bands near 1 and 2 μm, unless the samples have high Fe³⁺/Fe²⁺ ratios or are rich in Mn and Ca. Some of them (including unusual meteorite Angra dos Reis) are of type B despite very high Ca contents. We applied the Modified Gaussian Model (MGM) to characterize three major Fe²⁺ absorption bands in the 1-μm region of the spectra of Ca-rich pyroxenes. Only the band due to Fe²⁺ in the M1 coordination site near 1.15 μm may be potentially useful to estimate the Fe content in calcic pyroxenes on remotely-sensed surfaces of Solar System bodies. The spectral variability of basaltic meteorites (angrites) that are rich in calcic pyroxenes is also discussed. The presence of spectral type A calcic pyroxenes in these meteorites complicates unambiguous identification of olivine in asteroid spectra.     

Hydrated Silicates on M-, S-, and E-Type Asteroids as Possible Traces of Collisions with Bodies from the Jupiter Growth Zone

Absorption bands near 0.43 and 0.60–0.80 m, with a relative intensity of approximately 5–10%, were discovered in the reflectance spectra of five M asteroids (21, 75, 161, 201, and 497) and two S asteroids (11 and 198). It is highly probable that these absorption bands are related to oxidized and/or hydrated silicates that incorporate OH structural groups. Absorbed water in the surface material of about 24% of the known M asteroids and three E asteroids has been identified by a group of astronomers at the University of Arizona (Rivkin et al., 1995; Rivkin, 1997; Rivkin et al., 2000) on the basis of the characteristic 3-m absorption band. In addition to this, four of the six E-type asteroids observed spectrally in the visible region quite recently were found to have an absorption band at 0.5 m (Burbine et al., 1998; Fornasier and Lazzarin, 2001), which could likewise be associated with the presence of hydrated silicates in their material. The above data contradict the generally accepted viewpoint on the nature of M, S, and E asteroids, which is based on their common observed characteristics as bodies that arose at high temperatures (in the 1000–2000°C range). This contradiction, however, can be eliminated if use is made of the cosmogonic model developed by V.S. Safronov and co- workers. According to this model, the initial evolution of the main-belt asteroids was directly influenced by the process of the growth of Jupiter and was later controlled by its gravitational field.     

The 506 nm absorption feature in pyroxene spectra: Nature and implications for spectroscopy-based studies of pyroxene-bearing targets

High-resolution (0.34 nm) reflectance spectra of a suite of terrestrial ortho- and clinopyroxenes were characterized in the 506-nm region. This region exhibits absorption bands attributed to spin-forbidden transitions in Fe²⁺ located in the M2, and possibly M1, crystallographic site(s). The most intense absorption bands (up to 3.8% deep in <45 μm fractions) are present in low Ca-content orthopyroxene spectra. This region exhibits two (spectral Group I) or more (spectral Group II) absorption bands in the 500-515 nm interval. Group I spectra are associated with the lowest Ca-content samples. For orthopyroxenes, the number of constituent absorption bands and band depths vary as a function of Ca content; increasing Ca content results the appearance of more than two absorption bands and a general reduction in band depths, offsetting an expected increase in band depth with increasing Fe²⁺ content; band depths may also be reduced due to the long wavelength wing of ultraviolet region Fe-O charge transfer absorptions. Band depths and shapes in this region are also a function of grain size, with the strongest bands appearing for larger grain sizes - in the 90-250 μm range. The number and position of constituent absorption bands can be used to constrain factors such as cooling rates, as expressed in the formation of Guinier-Preston zones versus coarser-grained augite exsolution lamellae. Band depths in the spectra of fine-grained (<45 μm) clinopyroxenes do not exceed 1% and are generally lowest for spectral type A clinopyroxenes, where most of the Fe²⁺ is present in the M1 crystallographic site. The appearance of the 506 nm band in the spectra of pyroxene-bearing asteroids can be used to constrain pyroxene composition and structure. The results of this study suggest that detailed analysis of absorption features in the 506 nm region is a powerful tool for determining the composition and structure of pyroxenes. The spectral resolution of the VIR-MS spectrometer aboard the Dawn spacecraft - which will examine Asteroid 4 Vesta, a body possessing surficial pyroxenes - will be sufficient to provide some constraints on pyroxene composition.     

Spectral reflectance properties of minerals exposed to simulated Mars surface conditions

A number of mineral species were exposed to martian surface conditions of atmospheric pressure and composition, temperature, and UV light regime, and their evolution was monitored using reflectance spectroscopy. The stabilities for different groups varied widely. Phyllosilicate spectra all showed measurable losses of interlayer H₂O, with some structural groups showing more rapid H₂O loss than others. Loss of OH from the phyllosilicates is not always accompanied by a change in metal-OH overtone absorption bands. OH-bearing sulfates, such as jarosite and alunite, show no measurable change in spectral properties, suggesting that they should be spectrally detectable on Mars on the basis of diagnostic absorption bands in the 0.4-2.5 μm region. Fe³⁺- and H₂O-bearing sulfates all showed changes in the appearance and/or reduction in depths of hydroxo-bridged Fe³⁺ absorption bands, particularly at 0.43 μm. The spectral changes were often accompanied by visible color changes, suggesting that subsurface sulfates exposed to the martian surface environment may undergo measurable changes in reflectance spectra and color over short periods of time (days to weeks). Organic-bearing geological materials showed no measurable change in CH related absorption bands, while carbonates and hydroxides also showed no systematic changes in spectral properties. The addition of ultraviolet irradiation did not seem to affect mineral stability or rate of spectral change, with one exception (hexahydrite). In some cases, spectral changes could be related to the formation of specific new phases. The data also suggest that hydrated minerals detected on Mars to date retain their diagnostic spectral properties that allow their unique identification.     

Spectral reflectance‐compositional properties of spinels and chromites: Implications for planetary remote sensing and geothermometry

Abstract— Reflectance spectra of spinels and chromites have been studied as a function of composition. These two groups of minerals are spectrally distinct, which relates largely to differences in the types of major cations present. Both exhibit a number of absorption features in the 0.3–26 μm region that show systematic variations with composition and can be used to quantify or constrain certain compositional parameters, such as cation abundances, and site occupancies. For spinels, the best correlations exist between Fe²⁺ content and wavelength positions of the 0.46, 0.93, 2.8, Restrahelen, 12.3, 16.2, and 17.5 μm absorption features, Al and Fe³⁺ content with the wavelength position of the 0.93 μm absorption feature, and Cr content from the depth of the absorption band near 0.55 μm. For chromites, the best correlations exist between Cr content and wavelength positions of the 0.49, 0.59, 2, 17.5, and 23 μm absorption features, Fe²⁺ and Mg contents with the wavelength position of the 1.3 μm absorption feature, and Al content with the wavelength position of the 2 μm absorption feature. At shorter wavelengths, spinels and chromites are most readily distinguished by the wavelength position of the absorption band in the 2 μm region (<2.1 μm for spinels, >2.1 μm for chromite), while at longer wavelengths, spectral differences are more pronounced. The importance of being able to derive compositional information for spinels and chromites from spectral analysis stems from the relationship between composition and petrogenetic conditions (pressure, temperature, oxygen fugacity) and the widespread presence of spinels and chromites in the inner solar system. When coupled with the ability to derive compositional information for mafic silicates from spectral analysis, this opens up the possibility of deriving petrogenetic information for remote spinel‐ and chromite‐bearing targets from analysis of their reflectance spectra.     

Thermal metamorphism of CI and CM carbonaceous chondrites: An internal heating model

Abstract— Infrared diffuse reflectance spectra were measured for several thermally metamorphosed carbonaceous chondrites with CI-CM affinities which were recently found from Antarctica. Compared with other CI or CM carbonaceous chondrites, these Antarctic carbonaceous chondrites show weaker absorption bands near 3 μm due to hydrous minerals, and weaker absorption bands near 6.9 μm due to carbonates, interpreted as thermal metamorphic features. These absorption bands also disappear in the spectra of samples of the Murchison (CM) carbonaceous chondrite heated above 500 °C, implying that the metamorphic temperatures of the Antarctic carbonaceous chondrites considered here were higher than about 500 °C. Model calculations were performed to study thermal metamorphism of carbonaceous chondrites in a parent body internally heated by the decay of the extinct nuclide ²⁶Al. The maximum temperature of the interior of a body more than 20 km in radius is 500–700 °C for the bulk Al contents of CI and CM carbonaceous chondrites, assuming a ratio of ²⁶Al/²⁷Al = 5 × 10^?6 which has been previously proposed for an ordinary-chondrite parent body. The metamorphic temperatures experienced by the Antarctic carbonaceous chondrites considered here may be attainable by an internally heated body with an ²⁶Al/²⁷Al ratio similar to that inferred for an ordinary-chondrite parent body.     

Vesta: The first pyroxene band from new spectroscopic measurements

New spectral reflectance measurements of asteroid 4 Vesta were obtained using a silicon vidicon spectrometer with a resolution of 0.002–0.004 μm. The major absorption band in the near infrared has a minimum at 0.924 ± 0.004 μm with a bandwidth of 0.18 μm full width at half power (fwhp). The band represents a 30% absorption relative to peak reflectance at 0.75 μm. The absorption band has been interpreted to be due to electronic absorptions in ferrous iron in sixfold coordination in the pyroxene, pigeonite. The increased spectral resolution of these observations compared to earlier spectrophotometry enables us to refine the pyroxene composition, from the position of the Fe²⁺ absorption band, and arrive at a relative calcium content [Ca/(Mg + Fe + Ca)] of 10–12%. The absorption band is symmetric about its center, implying the presence of little or no olivine. The existence of the 2.0-μm pyroxene band which was verified by Larson and Fink (1975) confirms the interpretation based on the 1.0-μm band.     

Titanium-bearing pyroxenes of some E asteroids: Coexisting of igneous and hydrated rocks

In this paper, we present arguments for the presence of optically active Ti³⁺ in the structure of low iron pyroxenes to explain the strong 0.49-μm absorption band in spectra of E[II] asteroids. Such an interpretation supports the idea that E asteroid material is formed at high temperature in a strongly reducing medium. We also discuss the possibility of high temperature and hydrated rocks coexisting on some E asteroids. Our discussion is based on the idea of collisional evolution of aubrite parent bodies that was presented by Keil (1989).     

The composition of M-type asteroids: Synthesis of spectroscopic and radar observations

We have conducted a radar-driven observational campaign of 22 main-belt asteroids (MBAs) focused on Bus–DeMeo Xc- and Xk-type objects (Tholen X and M class asteroids) using the Arecibo radar and NASA Infrared Telescope Facilities (IRTF). Sixteen of our targets were near-simultaneously observed with radar and those observations are described in a companion paper (Shepard, M.K., and 19 colleagues [2010]. Icarus, in press). We find that most of the highest metal-content asteroids, as suggested by radar, tend to exhibit silicate absorption features at both 0.9 and 1.9 μm, and the lowest metal-content asteroids tend to exhibit either no bands or only the 0.9 μm band. Eleven of the asteroids were observed at several rotational longitudes in the near-infrared and significant variations in continuum slope were found for nine in the spectral regions 1.1–1.45 μm and 1.6–2.3 μm. We utilized visible wavelength data (Bus, S.J., Binzel, R.P. [2002b]. Icarus 158, 146–177; Fornasier, S., Clark, B.E., Dotto, E., Migliorini, A., Ockert-Bell, M., Barucci, M.A. [2010]. Icarus 210, 655–673.) for a more complete compositional analysis of our targets. Compositional evidence is derived from our target asteroid spectra using two different methods: (1) a χ² search for spectral matches in the RELAB database, and (2) parametric comparisons with meteorites. This paper synthesizes the results of the RELAB search and the parametric comparisons with compositional suggestions based on radar observations. We find that for six of the seven asteroids with the highest iron abundances, our spectral results are consistent with the radar evidence (16 Psyche, 216 Kleopatra, 347 Pariana, 758 Mancunia, 779 Nina, and 785 Zwetana). Three of the seven asteroids with the lowest metal abundances, our spectral results are consistent with the radar evidence (21 Lutetia, 135 Hertha, 497 Iva). The remaining seven asteroids (22 Kalliope, 97 Klotho, 110 Lydia, 129 Antigone, 224 Oceana, 678 Fredegundis, and 771 Libera) have ambiguous compositional interpretations when comparing the spectral analogs to the radar analogs. The number of objects with ambiguous results from this multi-wavelength survey using visible, near-infrared, and radar wavelengths indicates that perhaps a third diagnostic wavelength region (such as the mid-infrared around 2–4 μm, the mid-infrared around 10–15 μm, and/or the ultraviolet around 0.2–0.4 μm) should be explored to resolve the discrepancies.     

The rings of Saturn: New near-infrared reflectance measurements and a 0.326–4.08 μm summary

A new high photometric precision reflectance spectrum of Saturn's rings covering the spectral region 0.65 to 2.5-μm is presented and three previously unreported absorption features at 1.25, 0.85, and probably 1.04 μm are identified. The 1.25- and 1.04-μm absorptions are due to water ice. The 0.85-μm feature may be due to a combination of 0.81- and 0.90-μm ice absorptions but this feature appears too strong relative to the 1.04-μm band to be completely explained by weater ice. Another possibility is that the 0.85-μm band is due to Fe³⁺-bearing minerals in an ice-mineral mixture. This explanation could also account for the drop in the visible and ultraviolet reflectance and the rise in reflectance around 3.6 μm. Finally, a composite spectrum from 0.325 to 4.08 μm is presented which will be useful for future analysis and laboratory studies.