Distribution of HCN in Titan’s upper atmosphere from Cassini/VIMS observations at 3 μm

Cassini/VIMS limb observations have been used to retrieve vertical profiles of hydrogen cyanide (HCN) from its 3 μm emission in the region from 600 to 1100 km altitude at daytime. While the daytime emission is large up to about 1100 km, it vanishes at nighttime at very low altitudes, suggesting that the daytime emission originates under non-LTE conditions. The spectrally integrated radiances around 3.0 μm shows a monotonically decrease with tangent altitude, and a slight increase with solar zenith angle in the 40-80° interval around 800 km.A sophisticated non-LTE model of HCN energy levels has been developed in order to retrieve the HCN abundance. The population of the HCN 0 0⁰ 1 energy level, that contributes mostly to the 3.0 μm limb radiance, has been shown to change significantly with the solar zenith angle (SZA) and HCN abundance. Also its population varies with the collisional rate coefficients, whose uncertainties induced errors in the retrieved HCN of about 10% at 600-800 km and about 5% above. HCN concentrations have been retrieved from a set of spectra profiles, covering a wide range of latitudes and solar zenith angles, by applying a line-by-line inversion code. The results show a significant atmospheric variability above ∼800 km with larger values for weaker solar illumination. The HCN shows a very good correlation with solar zenith angles, irrespective of latitude and local time, suggesting that HCN at these high altitudes is in or close to photochemical equilibrium. A comparison with UVS and UVIS measurements show that these are close to the lower limit (smaller SZAs) of the VIMS observations above 750 km. However, they are in reasonable agreement when combining the rather large UV measurement errors and the atmospheric variability observed in VIMS. A comparison of the mean profile derived here with the widely used profile reported by Yelle and Griffith (Yelle R.V., Griffith, C.A. [2003]. Icarus 166, 107-115) shows a good agreement for altitudes ranging from 850 to 1050 km, while below these altitudes our result exhibits higher concentrations.     

Saturn’s tropospheric composition and clouds from Cassini/VIMS 4.6-5.1 μm nightside spectroscopy

The latitudinal variation of Saturn’s tropospheric composition (NH₃, PH₃ and AsH₃) and aerosol properties (cloud altitudes and opacities) are derived from Cassini/VIMS 4.6-5.1 μm thermal emission spectroscopy on the planet’s nightside (April 22, 2006). The gaseous and aerosol distributions are used to trace atmospheric circulation and chemistry within and below Saturn’s cloud decks (in the 1- to 4-bar region). Extensive testing of VIMS spectral models is used to assess and minimise the effects of degeneracies between retrieved variables and sensitivity to the choice of aerosol properties. Best fits indicate cloud opacity in two regimes: (a) a compact cloud deck centred in the 2.5-2.8 bar region, symmetric between the northern and southern hemispheres, with small-scale opacity variations responsible for numerous narrow light/dark axisymmetric lanes; and (b) a hemispherically asymmetric population of aerosols at pressures less than 1.4 bar (whose exact altitude and vertical structure is not constrained by nightside spectra) which is 1.5-2.0× more opaque in the summer hemisphere than in the north and shows an equatorial maximum between ±10° (planetocentric).Saturn’s NH₃ spatial variability shows significant enhancement by vertical advection within ±5° of the equator and in axisymmetric bands at 23-25°S and 42-47°N. The latter is consistent with extratropical upwelling in a dark band on the poleward side of the prograde jet at 41°N (planetocentric). PH₃ dominates the morphology of the VIMS spectrum, and high-altitude PH₃ at p < 1.3 bar has an equatorial maximum and a mid-latitude asymmetry (elevated in the summer hemisphere), whereas deep PH₃ is latitudinally-uniform with off-equatorial maxima near ±10°. The spatial distribution of AsH₃ shows similar off-equatorial maxima at ±7° with a global abundance of 2-3 ppb. VIMS appears to be sensitive to both (i) an upper tropospheric circulation (sensed by NH₃ and upper-tropospheric PH₃ and hazes) and (ii) a lower tropospheric circulation (sensed by deep PH₃, AsH₃ and the lower cloud deck).     

Characterization of Titan’s Ontario Lacus region from Cassini/VIMS observations

Liquid hydrocarbons were long predicted on Titan’s surface before the RADAR instrument onboard Cassini detected lakes poleward of 70°N in July 2006. Before that the Cassini Imaging Science Subsystem (ISS) observed a lake-like feature in the South Pole, named Ontario Lacus, in July 2004. Here we analyze one observation of Ontario Lacus taken by the Visual and Infrared Mapping Spectrometer (VIMS) on 2007 December 5, during the T 38 flyby. This is the best spatially resolved image of a Titan lake to date by an imaging spectrometer, and has been previously reported in Brown et al. (Brown, R.H., Soderblom, L.A., Soderblom, J.M., Clark, R.N., Jaumann, R., Barnes, J.W., Sotin, C., Buratti, B., Baines, K.H., Nicholson, P.D. [2008]. Nature 454, 607–610) and in Barnes et al. (Barnes, J.W. et al. [2009]. Icarus 201, 217–225). The observing geometry and our data processing will be explained, followed by a discussion of the main characteristics of the image. The analyzed image covers a small portion of Ontario Lacus and shows what appears from RADAR data to be a region of modest slope (“ramp”) adjacent to the dark lake itself. Our analysis of 5.0 μm spectral data suggests that the previously reported absorption feature of ethane seen at shorter wavelengths may be produced by damp sediments adjacent to the main liquid basin. The latter appears to be absorbing all of the photons incident upon it in the 5 μm spectral region and shows no discernible absorption features. A characterization of the basin composition and morphology is developed with the help of ISS and RADAR observations. The simplest model consistent with the data is an optically deep lake surrounded by a region in which ethane, propane, possibly methane, and other, less volatile hydrocarbons and nitriles are present mixed into spectroscopically neutral sediments. The dominance of relatively low vapor pressure organics outside the lake itself suggests a retreat of Ontario Lacus associated with evaporation on seasonal or longer timescales, consistent with analysis of RADAR and ISS images.     

The gas composition of jupiter derived from 5-μm airborne spectroscopic observations

The atmospheric transmission window between 1850 and 2250 cm⁻¹ in Jupiter's atmosphere was observed at a spectral resolution of 0.5 cm⁻¹ from the Kuiper Airborne Observatory. The mole fractions of NH₃, PH₃, CH₄, CH₃D, CO, and GeH₄ were derived for the 1- to 6-bar portion of Jupiter's troposphere using a spectrum synthesis program. Knowledge of the abundances of these gases below the visible clouds is necessary to calculate the global inventory of nitrogen, phosphorus, carbon, and deuterium, which, in turn, may constrain models of Jupiter's formation. The N/H ratio is 1.5 ± 0.2 times the value for the Sun's photosphere. The P/H ratio for the 5-bar level is between 1.0 and 1.6 times the solar abundance. The weak ν₃−ν₄ hot band of CH₄ was detected for the first time on Jupiter, thus providing a deep atmospheric value for C/H of 3.6 ± 1.2 times solar. The Jovian deuterium abundance is comparable to that measured in the interstellar medium (D/H = 1.2 ± 0.5) × 10⁻⁵. CO appears to be well mixed with a mole fraction of (1.0 ± 0.3) × 10⁻⁹. Multiple absorption features confirm that GeH₄ is present on Jupiter with a mole fraction of (7.0_−2.0^+4.0) × 10⁻¹⁰. The observed abundances of CO, GeH₄, and PH₃ are consistent with models of convective transport from Jupiter's deep atmosphere.     

Phosphine absorption in the 5-μm window of Jupiter

Since the original suggestion by Gillett et al. (1969) it has generally been assumed that the region of partial transparency near 5 μm in Jupiter's atmosphere (the 5-μm window) is bounded by the v₄ NH₃ at 6.1 μm and the v₃ CH₄ band at 3.3 μm. New measurements of Jupiter and of laboratory phosphine (PH₃) samples show that PH₃ is a significant contributor to the continuum opacity in the window and in fact defines its short-wavelength limit. This has important implications for the use of 5-mu;m observations as a means to probe the deep atmospheric structure of Jupiter. The abundance of PH₃ which results from a comparison of Jovian and laboratory spectra is about 3 to 5 cm-am. This is five to eight times less than that found by Larson et al. [Astrophys. J. (1977) 211, 972–979] in the same spectral region, but is in good agreement with the result of Tokunaga et al. [Astrophys. J. (1979) 232, 603–615] from 10-μm observations.     

The 2–4-μm spectrum of Saturn's rings

Observations of the rings of Saturn at 2–4 μm reveal the presence of a 3.6-μm peak in the infrared reflectivity. This peak is consistent with a particle size of ? 50 μm, and a composition of pure H₂O ice. The quoted size may only be indicative of the textural scale of frost on the surface of larger particles. The presence of small amounts of CH₄ in the form of a clathrate, however, cannot be ruled out by our measurements.     

Analysis of Titan CH4 3.3 μm upper atmospheric emission as measured by Cassini/VIMS

After molecular nitrogen, methane is the most abundant species in Titan’s atmosphere and plays a major role in its energy budget and its chemistry. Methane has strong bands at 3.3 μm emitting mainly at daytime after absorption of solar radiation. This emission is strongly affected by non-local thermodynamic equilibrium (non-LTE) in Titan’s upper atmosphere and, hence, an accurate modeling of the non-LTE populations of the emitting vibrational levels is necessary for its analysis. We present a sophisticated and extensive non-LTE model which considers 22 CH₄ levels and takes into account all known excitation mechanisms in which they take part. Solar absorption is the major excitation process controlling the population of the v₃-quanta levels above 1000 km whereas the distribution of the vibrational energy within levels of similar energy through collisions with N₂ is also of importance below that altitude. CH₄-CH₄ vibrational exchange of v₄-quanta affects their population below 500 km. We found that the ν₃ → ground band dominates Titan’s 3.3 μm daytime limb radiance above 750 km whereas the ν₃ + ν₄ → ν₄ band does below that altitude and down to 300 km. The ν₃ + ν₂ → ν₂, the 2ν₃ → ν₃, and the ¹³CH₄ν₃ → ground bands each contribute from 5% to 8% at regions below 800 km. The ν₃ + 2ν₄ → 2ν₄and ν₂ + ν₃ + ν₄ → ν₂ + ν₄ bands each contribute from 2% to 5% below 650 km. Contributions from other CH₄ bands are negligible. We have used the non-LTE model to retrieve the CH₄ abundance from 500 to 1100 km in the southern hemisphere from Cassini-VIMS daytime measurements near 3.3 μm. Our retrievals show good agreement with previous measurements and model results, supporting a weak deviation from well mixed values from the lower atmosphere up to 1000 km.     

Cassini spectra and photometry 0.25-5.1 μm of the small inner satellites of Saturn

The nominal tour of the Cassini mission enabled the first spectra and solar phase curves of the small inner satellites of Saturn. We present spectra from the Visual Infrared Mapping Spectrometer (VIMS) and the Imaging Science Subsystem (ISS) that span the 0.25-5.1 μm spectral range. The composition of Atlas, Pandora, Janus, Epimetheus, Calypso, and Telesto is primarily water ice, with a small amount (∼5%) of contaminant, which most likely consists of hydrocarbons. The optical properties of the “shepherd” satellites and the coorbitals are tied to the A-ring, while those of the Tethys Lagrangians are tied to the E-ring of Saturn. The color of the satellites becomes progressively bluer with distance from Saturn, presumably from the increased influence of the E-ring; Telesto is as blue as Enceladus. Janus and Epimetheus have very similar spectra, although the latter appears to have a thicker coating of ring material. For at least four of the satellites, we find evidence for the spectral line at 0.68 μm that Vilas et al. [Vilas, F., Larsen, S.M., Stockstill, K.R., Gaffley, M.J., 1996. Icarus 124, 262-267] attributed to hydrated iron minerals on Iapetus and Hyperion. However, it is difficult to produce a spectral mixing model that includes this component. We find no evidence for CO₂ on any of the small satellites. There was a sufficient excursion in solar phase angle to create solar phase curves for Janus and Telesto. They bear a close similarity to the solar phase curves of the medium-sized inner icy satellites. Preliminary spectral modeling suggests that the contaminant on these bodies is not the same as the exogenously placed low-albedo material on Iapetus, but is rather a native material. The lack of CO₂ on the small inner satellites also suggests that their low-albedo material is distinct from that on Iapetus, Phoebe, and Hyperion.     

Upper limits to trace constituents in Jupiter's atmosphere from an analysis of its 5-μm spectrum

A high-resolution (0.6 cm^?1) spectrum of Jupiter at 5 μm recorded at the Kuiper Airborne Observatory is used to determine upper limits to the column density of 19 molecules. The upper limits to the mixing ratios of SiH₄, H₂S, HCN, and simple hydrocarbons are discussed with respect to current models of Jupiter's atmosphere. These upper limits are compared to expectations based upon the solar abundance of the elements. This analysis permits upper limit measurements (SiH₄), or actual detections (GeH₄), of molecules with mixing ratios with hydrogen as low as 10^?9. In future observations at 5 μm the sensitivity of remote spectroscopic analyses should permit the study of constituents with mixing ratios as low as 10^?10, which would include the hydrides of such elements as Sn and As as well as numerous organic molecules.     

Titan’s aerosol and stratospheric ice opacities between 18 and 500 μm: Vertical and spectral characteristics from Cassini CIRS

Vertical distributions and spectral characteristics of Titan’s photochemical aerosol and stratospheric ices are determined between 20 and 560 cm^?1 (500–18 μm) from the Cassini Composite Infrared Spectrometer (CIRS). Results are obtained for latitudes of 15°N, 15°S, and 58°S, where accurate temperature profiles can be independently determined.In addition, estimates of aerosol and ice abundances at 62°N relative to those at 15°S are derived. Aerosol abundances are comparable at the two latitudes, but stratospheric ices are ～3 times more abundant at 62°N than at 15°S. Generally, nitrile ice clouds (probably HCN and HC₃N), as inferred from a composite emission feature at ～160 cm^?1, appear to be located over a narrow altitude range in the stratosphere centered at ～90 km. Although most abundant at high northern latitudes, these nitrile ice clouds extend down through low latitudes and into mid southern latitudes, at least as far as 58°S.There is some evidence of a second ice cloud layer at ～60 km altitude at 58°S associated with an emission feature at ～80 cm^?1. We speculate that the identify of this cloud may be due to C₂H₆ ice, which in the vapor phase is the most abundant hydrocarbon (next to CH₄) in the stratosphere of Titan.Unlike the highly restricted range of altitudes (50–100 km) associated with organic condensate clouds, Titan’s photochemical aerosol appears to be well-mixed from the surface to the top of the stratosphere near an altitude of 300 km, and the spectral shape does not appear to change between 15°N and 58°S latitude. The ratio of aerosol-to-gas scale heights range from 1.3–2.4 at about 160 km to 1.1–1.4 at 300 km, although there is considerable variability with latitude. The aerosol exhibits a very broad emission feature peaking at ～140 cm^?1. Due to its extreme breadth and low wavenumber, we speculate that this feature may be caused by low-energy vibrations of two-dimensional lattice structures of large molecules. Examples of such molecules include polycyclic aromatic hydrocarbons (PAHs) and nitrogenated aromatics.Finally, volume extinction coefficients Nχ_E derived from 15°S CIRS data at a wavelength of λ = 62.5 μm are compared with those derived from the 10°S Huygens Descent Imager/Spectral Radiometer (DISR) data at 1.583 μm. This comparison yields volume extinction coefficient ratios Nχ_E(1.583 μm)/Nχ_E(62.5 μm) of roughly 70 and 20, respectively, for Titan’s aerosol and stratospheric ices. The inferred particle cross-section ratios χ_E(1.583 μm)/χ_E(62.5 μm) appear to be consistent with sub-micron size aerosol particles, and effective radii of only a few microns for stratospheric ice cloud particles.     

Rotationally-resolved spectra of Ceres in the 3-μm region

We present observations of Ceres over the 2.2-4.0 μm region taken using the SpeX instrument on the NASA IRTF in 2005. The observations cover Ceres’ entire longitude range and show evidence for a relatively uniform surface in terms of Ceres’ composition, however there is a subtle but consistently shallower band depth over longitudes associated with bright regions in HST maps, suggesting those areas are slightly less carbonate- and brucite-rich. We also find Ceres’ beaming parameter, a measure of its thermal properties, to have changed with its viewing aspect.     

The 10- and 20-μm interstellar absorption bands: Comparison with the infrared spectrum of the Nogoya meteorite

For submicrometer-sized particles of the carbonaceous chondrite Nogoya and, for comparison purposes, also of terrestrial chamosite, the mass absorption coefficients have been derived from laboratory spectra for the wavenumber range 250–1300 cm^–1. Using these data the expected spectrum of an infrared source has been calculated under simple model assumptions and compared with the observed flux from the infrared source OH 26.5+0.6. Although certain discrepancies are left in the 20-m region it is concluded that phyllosilicates, especially such occurring in carbonaceous chondrites, are interesting candidates for the material of interstellar grains.     

High-resolution 3-μm spectra of Jupiter: Latitudinal spectral variations influenced by molecules, clouds, and haze

We present latitudinally-resolved high-resolution (R = 37,000) pole-to-pole spectra of Jupiter in various narrow longitudinal ranges, in spectral intervals covering roughly half of the spectral range 2.86-3.53 μm. We have analyzed the data with the aid of synthetic spectra generated from a model jovian atmosphere that included lines of CH₄, CH₃D, NH₃, C₂H₂, C₂H₆, PH₃, and HCN, as well as clouds and haze. Numerous spectral features of many of these molecular species are present and are individually identified for the first time, as are many lines of and a few unidentified spectral features. In both polar regions the 2.86-3.10-μm continuum is more than 10 times weaker than in spectra at lower latitudes, implying that in this wavelength range the single-scattering albedos of polar haze particles are very low. In contrast, the 3.24-3.53 μm the weak polar and equatorial continua are of comparable intensity. We derive vertical distributions of NH₃, C₂H₂ and C₂H₆, and find that the mixing ratios of NH₃ and C₂H₆ show little variation between equatorial and polar regions. However, the mixing ratios of C₂H₂ in the northern and southern polar regions are ∼6 and ∼3 times, respectively, less than those in the equatorial regions. The derived mixing ratio curves of C₂H₂ and C₂H₆ extend up to the 10⁻⁶ bar level, a significantly higher altitude than most previous results in the literature. Further ground-based observations covering other longitudes are needed to test if these mixing ratios are representative values for the equatorial and polar regions.     

Quantification of middle and lower cloud variability and mesoscale dynamics from Venus Express/VIRTIS observations at 1.74 μm

We present an analysis of VIRTIS-M-IR observations of 1.74 μm emission from the nightside of Venus. The 1.74 μm window in the near infrared spectrum of Venus is an ideal proxy for investigating the evolution of middle and lower cloud deck opacity of Venus because it exhibits good signal to noise due to its brightness, good contrast between bright and dark regions, and few additional sources of extinction beside the clouds themselves. We have analyzed the data from the first 407 orbits (equivalent to 407 Earth days) of the Venus Express mission to determine the magnitude of variability in the 1.74 μm radiance. We have also performed an analysis of the evolution of individual features over a span of roughly 5–6 h on two successive orbits of Venus Express. We find that the overall 1.74 μm brightness of Venus has been increasing through the first 407 days of the mission, indicating a gradual diminishing of the cloud coverage and/or thickness, and that the lower latitudes exhibited more variability and more brightening than higher latitudes. We find that individual features evolve with a time scale of about 30 h, consistent with our previous analysis. Analysis of the evolution and motion of the clouds can be used to estimate the mesoscale dynamics within the clouds of Venus. We find that advection alone cannot explain the observed evolution of the features. The measured vorticity and divergence in the vicinity of the features are consistent with evolution under the influence of significant vertical motions likely driven by a radiative dynamical feedback. We measure a zonal wind speed of around 65 m/s, and a meridional wind speed around 2.5 m/s by tracking the motion of the central region of the features. But we also find that the measured wind speeds depend strongly on the points chosen for the wind speed analysis.     

Optical constants of Titan’s stratospheric aerosols in the 70–1500 cm−1 spectral range constrained by Cassini/CIRS observations

We utilized aerosol extinction coefficient inferred from Cassini/CIRS spectra in the far and mid infrared region to derive the extinction cross-section near an altitude of 190 km at 15°S (from far-IR) and 20°S (from mid-IR). By comparing the extinction cross section that are derived from observations with theoretical calculations for a fractal aggregate of 3000 monomers, each having a radius of 0.05 μm, and a fractal dimension of 2, we are able to constrain the refractive index of Titan’s aerosol between 70 and 1500 cm^?1 (143 and 6.7 μm). As the real and imaginary parts of the refractive index are related by the Kramers–Kronig equation, we apply an iterative process to determine the optical constants in the thermal infrared. The resulting spectral dependence of the imaginary index displays several spectral signatures, some of which are also seen for some Titan’s aerosol analogues (tholins) produced in laboratory experiments. We find that Titan’s aerosols are less absorbent than tholins in the thermal infrared. The most prominent emission bands observed in the mid-infrared are due to CH bending vibrations in methyl and methylene groups. It appears that Titan’s aerosols predominantly display vibrations implying carbon and hydrogen atoms and perhaps marginally nitrogen. In the mid infrared, all the aerosol spectral signatures are observed at three additional latitudes (56°S, 5°N and 30°N) and in the 193–274 km altitude range, which implies that Titan’s aerosols exhibit the same chemical composition in all investigated latitude and altitude regions.     

Retrieval and tentative indentification of the 3 μm spectral feature in Titan's haze

Recently, an unidentified 3.3-3.4 μm feature found in the solar occultation spectra of the atmosphere of Titan observed by Cassini/VIMS was tentatively attributed to the C-H stretching mode of aliphatic hydrocarbon chains attached to large organic molecules, but without properly extracting the feature from adjacent influences of strong CH₄ and weak C₂H₆ absorptions (Bellucci et al., 2009). In this work, we retrieve the detailed spectral feature using a radiative transfer program including absorption and fluorescent emission of both molecules, as well as absorption and scattering by haze particles. The spectral features of the haze retrieved from the VIMS data at various altitudes are similar to each other, indicating relatively uniform spectral properties of the haze with altitude. However, slight deviations observed near 127 km and above 300 km suggest inhomogeneity at these altitudes. We find that the positions of the major spectral peaks occur at 3.33-3.37 μm, which are somewhat different from the typical 3.3 μm aromatic or 3.4 μm aliphatic C-H stretches usually seen in the spectra of dust particles of the interstellar medium and comets. The peaks, however, coincide with those of the solid state spectra of C₂H₆, CH₄, and CH₃CN; and a broad shoulder from 3.37 to 3.50 μm coincides with those of C₅H₁₂ and C₆H₁₂ as well as those of typical aliphatic C-H stretches. This result combined with high-altitude (∼1000 km) haze formation process recently reported by Waite et al. (2007) opens a new question on the chemical composition of the haze particles. We discuss the possibility that the 3 μm feature may be due to the solid state absorption bands of these molecules (or some other molecules) and we advocate additional laboratory measurements for the ices of hydrocarbon and nitrogen-bearing molecules present in Titan's atmosphere for the identification of this 3 μm feature.     

Assessing the spatial variability of the ~3 μm OH/H2O absorption feature in CM2 carbonaceous chondrites

H₂O and OH are readily detected in hydrated minerals in CM chondrites via reflectance spectroscopy due to their characteristic vibration absorptions at infrared wavelengths. Previous spectroscopic work on bulk powdered CM chondrites has shown that spectral parameters, like the wavelength position of the “3 μm absorption feature,” vary systematically with the extent to which the samples have been aqueously altered. However, it is yet unclear how these spectral features may vary across an intact meteorite chip when measured at spatial scales smaller than that of the individual components of the meteorite. Here, we explore the spatial variability of this spectral feature and others on intact CM2 chips which, unlike powders, retain their petrologic and textural characteristics. We also model the modal mineralogy of the bulk meteorite powders and correlate this with key spectral features, demonstrating that microscope Fourier transform infrared spectroscopic mapping provides a powerful, rapid, and non-destructive technique for assessing compositional diversity and variations in water–rock interactions in chondritic planetary materials. In all CM2 chondrites studied here, we find that variations in the position, shape, and strength of the 3 μm absorption feature reveal a single chondrite can exhibit as much spectral variation as the entire suite of CM2 chondrites. The observed variations in the position and shape of the 3 μm feature within individual CM2 chondrite chips suggest a range of alteration products (e.g., Mg-rich to Fe-rich phyllosilicates) are present and record sub-mm scale variations in the amount and/or chemistry of the altering fluids. The samples having experienced the most progressive aqueous alteration show the least amount of variability in features like the 3 μm absorption band minimum position, whereas the least altered samples exhibit the most variability. We also find that the bulk spectral signatures in the least altered samples appear to be biased toward the spectral signatures of clasts versus matrix. By extension, asteroid reflectance spectra exhibiting 3 μm absorption features consistent with those measured here may be interpreted in a similar framework in which the spectrum of what may appear to be the least altered asteroids represents an average that belies the true diversity of mineralogy and chemistry of the body.     

Outer Main Belt asteroids: Identification and distribution of four 3-μm spectral groups

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.     

Eclipse reappearances of Io: Time-resolved spectroscopy (1.9-4.2 μm)

We obtained time-resolved, near-infrared spectra of Io during the 60-90 min following its reappearance from eclipse by Jupiter on five occasions in 2004. The purpose was to search for spectral changes, particularly in the well-known SO₂ frost absorption bands, that would indicate surface-atmosphere exchange of gaseous SO₂ induced by temperature changes during eclipse. These observations were a follow-on to eclipse spectroscopy observations in which Bellucci et al. [Bellucci et al., 2004. Icarus 172, 141-148] reported significant changes in the strengths of two strong SO₂ bands in data acquired with the VIMS instrument aboard the Cassini spacecraft. One of the bands (4.07 μm [ν₁ + ν₃]) observed by Bellucci et al. is visible from ground-based observatories and is included in our data. We detected no changes in Io’s spectrum at any of the five observed events during the approximately 60-90 min during which spectra were obtained following Io’s emergence from Jupiter’s shadow. The areas of the three strongest SO₂ bands in the region 3.5-4.15 μm were measured for each spectrum; the variation of the band areas with time does not exceed that which can be explained by the Io’s few degrees of axial rotation during the intervals of observation, and in no case does the change in band strength approach that seen in the Cassini VIMS data. Our data are of sufficient quality and resolution to show the weak 2.198 μm (4549.6 cm⁻¹) 4ν₁ band of SO₂ frost on Io for what we believe is the first time. At one of the events (June 22, 2004), we began the acquisition of spectra ∼6 min before Io reappeared from Jupiter’s shadow, during which time it was detected through its own thermal emission. No SO₂ bands were superimposed on the purely thermal spectrum on this occasion, suggesting that the upper limit to condensed SO₂ in the vertical column above Io’s surface was ∼4 × 10⁻⁵ g cm⁻².