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.     

Saturn’s F ring grains: Aggregates made of crystalline water ice

We present models of the near-infrared (1-5 μm) spectra of Saturn’s F ring obtained by Cassini’s Visual and Infrared Mapping Spectrometer (VIMS) at ultra-high phase angles (177.4-178.5°). Modeling this spectrum constrains the size distribution, composition, and structure of F ring particles in the 0.1-100 μm size range. These spectra are very different from those obtained at lower phase angles; they lack the familiar 1.5 and 2 μm absorption bands, and the expected 3 μm water ice primary absorption appears as an unusually narrow dip at 2.87 μm. We have modeled these data using multiple approaches. First, we use a simple Mie scattering model to constrain the size distribution and composition of the particles. The Mie model allows us to understand the overall shapes of the spectra in terms of dominance by diffraction at these ultra-high phase angles, and also to demonstrate that the 2.87 μm dip is associated with the Christiansen frequency of water ice (where the real refractive index passes unity). Second, we use a combination of Mie scattering with Effective Medium Theory to probe the effect of porous (but structureless) particles on the overall shape of the spectrum and depth of the 2.87 μm band. Such simple models are not able to capture the shape of this absorption feature well. Finally, we model each particle as an aggregate of discrete monomers, using the Discrete Dipole Approximation (DDA) model, and find a better fit for the depth of the 2.87 μm feature. The DDA models imply a slightly different overall size distribution. We present a simple heuristic model which explains the differences between the Mie and DDA model results. We conclude that the F ring contains aggregate particles with a size distribution that is distinctly narrower than a typical power law, and that the particles are predominantly crystalline water ice.     

Near-infrared spectroscopy of primitive asteroid families

We compare 13 near-infrared (0.8-2.4 μm) spectra of two low albedo C complex outer-belt asteroid families: Themis and Veritas. The disruption ages of these two families lie at opposite extremes: 2.5 ± 1.0 Gyr and 8.7 ± 1.7 Myr, respectively. We found striking differences between the two families, which show a range of spectral shapes and slopes. The seven Themis family members (older surfaces) have “red” (positive) slopes in the 1.6-2.4 μm region; in contrast, the six Veritas members (younger surfaces) have significantly “flatter” slopes at these same wavelengths. Moreover, the two families are characterized by different concavity at shorter (1.0-1.5 μm) wavelengths with the Themis group being consistently flat or concave up (smile) and the Veritas group being consistently concave down (frown). Each family contains a broad range of diameters, suggesting our results are not due to comparisons of asteroids of different sizes. The statistically significant clustering of the two spectral groups could be explained by one of the following three possibilities or a combination of them: (1) space weathering effects, (2) differences in original composition, or (3) differences in thermal history perhaps as a result of the difference in parent body sizes. As a result of our analyses, we propose a new method to quantify broad and shallow structures in the spectra of primitive asteroids. We found reasonable matches between the observed asteroids and individual carbonaceous chondrite meteorites. Because these meteoritic fits represent fresh surfaces, space weathering is neither necessary nor ruled out as an explanation of spectral differences between families. The six Veritas family near-infrared (NIR) spectra represent the first NIR analysis of this family, thus significantly increasing our understanding of this family over these wavelengths.     

The origin of (90) Antiope from component-resolved near-infrared spectroscopy

The origin of the similarly-sized binary Asteroid (90) Antiope remains an unsolved puzzle. To constrain the origin of this unique double system, we recorded individual spectra of the components using SPIFFI, a near-infrared integral field spectrograph fed by SINFONI, an adaptive optics module available on VLT-UT4. Using our previously published orbital model, we requested telescope time when the separation of the components of (90) Antiope was larger than 0.087″, to minimize the contamination between components, during the February 2009 opposition. Several multi-spectral data-cubes in J band (SNR = 40) and H + K band (SNR = 100) were recorded in three epochs and revealed the two components of (90) Antiope. After developing a specific photometric extraction method and running an error analysis by Monte-Carlo simulations, we successfully extracted reliable spectra of both components from 1.1 to 2.4 μm taken on the night of February 21, 2009. These spectra do not display any significant absorption features due to mafic mineral, ices, or organics, and their slopes are in agreement with both components being C- or Cb-type asteroids. Their constant flux ratio indicates that both components’ surface reflectances are quite similar, with a 1-sigma variation of 7%. By comparison with 2MASS J, H, K color distribution of observed Themis family members, we conclude that both bodies were most likely formed at the same time and from the same material. The similarly-sized system could indeed be the result of the breakup of a rubble-pile proto-Antiope into two equal-sized bodies, but other scenarios of formation implying a common origin should also be considered.     

The aftermath of the July 2009 impact on Jupiter: Ammonia, temperatures and particulates from Gemini thermal infrared spectroscopy

We obtained longitudinally resolved thermal infrared spectra (8-13 μm and 17-25 μm) of Jupiter’s impact debris at the Gemini South Telescope on July 24, 2009; five days after the July 19th collision. These were used to study the mechanisms responsible for the redistribution of thermal energy and material (ammonia and stratospheric particulates) following the impact. Upwelling of (8.5 ± 4.1) × 10¹⁴ g of tropospheric air was sufficient to deposit (6.7 ± 4.1) × 10¹² g of NH₃ over a 6° longitude range above the impact core. The NH₃ was distributed over the 20-80 mbar region with a peak abundance of 1.0 ± 0.6 ppm at 45 mbar. Only a 10th of this abundance was observed over the western ejecta, and it is unlikely that these observations were sensitive to NH₃ entrained in the ballistic plume itself. The pattern of excess thermal energy was markedly different from that of Shoemaker-Levy 9 (SL9), with a localized tropospheric perturbation of 2.0 ± 1.0 K at 200-300 mbar and a broader stratospheric warming of up to 3.5 ± 2.0 K at 10-30 mbar. We find no evidence of residual warmth at p < 1 mbar five days after the impact. The excess thermal energy places lower limits on the total energy of the impact (1.8-15.7 × 10²⁶ ergs), which limits the impactor diameter to 70-510 m (depending on the bulk density chosen for the material).The models of the Gemini spectra required three distinct aerosol features, indicative of the mineralogy of the dark particulate debris, centred at 9.1, 10.0 and 18.5 μm. The retrieved opacities for each of these features were distributed over a larger area (9-10° longitude) and at higher altitudes (above the 10-mbar level) than the stratospheric NH₃, and they are more spatially inhomogeneous. This implies the particulates were either entrained with the rising hot plume or created upon plume re-entry and are subsequently redistributed by stratospheric winds. The three particulate features were consistent with a mixture of amorphous iron and magnesium-rich silicates and silicas in the debris field. A broad 10-μm signature was coincident with peaks expected from material rich in amorphous olivines (but poor in pyroxenes), and similar to silicate features observed during SL9. A narrow 9.1-μm signature was interpreted as a combination of amorphous and crystalline silica. Finally, a broad 18.5-μm emitter was not adequately reproduced by a mixture of simple olivines and pyroxenes and remains to be identified.     

Europa’s ridged plains and smooth low albedo plains: Distinctive compositions and compositional gradients at the leading side-trailing side boundary

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.     

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.     

An improvement to the volcano-scan algorithm for atmospheric correction of CRISM and OMEGA spectral data

The observations of Mars by the CRISM and OMEGA hyperspectral imaging spectrometers require correction for photometric, atmospheric and thermal effects prior to the interpretation of possible mineralogical features in the spectra. Here, we report on a simple, yet non-trivial, adaptation to the commonly-used volcano-scan correction technique for atmospheric CO₂, which allows for the improved detection of minerals with intrinsic absorption bands at wavelengths between 1.9 and 2.1 μm. This volcano-scan technique removes the absorption bands of CO₂ by ensuring that the Lambert albedo is the same at two wavelengths: 1.890 and 2.011 μm, with the first wavelength outside the CO₂ gas bands and the second wavelength deep inside the CO₂ gas bands. Our adaptation to the volcano-scan technique moves the first wavelength from 1.890 μm to be instead within the gas bands at 1.980 μm, and for CRISM data, our adaptation shifts the second wavelength slightly, to 2.007 μm. We also report on our efforts to account for a slight ∼0.001 μm shift in wavelengths due to thermal effects in the CRISM instrument.     

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.     

Mid-infrared reflectance spectra and optical constants of six iron oxide/oxyhydroxide phases

We have determined the real and imaginary indices of refraction (n and k) for six iron oxide/oxyhydroxide phases—magnetite, maghemite, goethite, lepidocrocite, akaganéite, and ferrihydrite. A single crystal of magnetite was used to derive bulk n and k values from 100-2000 cm⁻¹ (5-100 μm). Synthetic nanocrystalline samples of maghemite, goethite, lepidocrocite, akaganéite, and ferrihydrite were pressed into compact pellets used to determine bulk n and k values from 100-1200 cm⁻¹ (8.33-100 μm). All values of n and k (the optical constants) were determined from specular reflectance spectra acquired at 2 cm⁻¹ spectral sampling using classical Lorentz-Lorenz dispersion theory. In this paper, we present the optical constants of all six minerals and the oscillator parameters with which they were modeled. Use of these optical constants could aid in radiative transfer models of terrestrial dust as well as Mars, the Moon, and airless bodies in the Solar System.     

Radiation-induced amorphization of crystalline ice

We study radiation-induced amorphization of crystalline ice, analyzing the results of three decades of experiments with a variety of projectiles, irradiation energy, and ice temperature, finding a similar trend of increasing resistance of amorphization with temperature and inconsistencies in results from different laboratories. We discuss the temperature dependence of amorphization in terms of the ‘thermal spike’ model. We then discuss the common use of the 1.65 μm infrared absorption band of water as a measure of degree of crystallinity, an increasingly common procedure to analyze remote sensing data of astronomical icy bodies. The discussion is based on new, high quality near-infrared reflectance absorption spectra measured between 1.4 and 2.2 μm for amorphous and crystalline ices irradiated with 225 keV protons at 80 K. We found that, after irradiation with 10¹⁵ protons cm⁻², crystalline ice films thinner than the ion range become fully amorphous, and that the infrared absorption spectra show no significant changes upon further irradiation. The complete amorphization suggests that crystalline ice observed in the outer Solar System, including trans-neptunian objects, may results from heat from internal sources or from the impact of icy meteorites or comets.     

The source of widespread 3-μm absorption in Jupiter’s clouds: Constraints from 2000 Cassini VIMS observations

The Cassini flyby of Jupiter in 2000 provided spatially resolved spectra of Jupiter’s atmosphere using the Visual and Infrared Mapping Spectrometer (VIMS). A prominent characteristic of these spectra is the presence of a strong absorption at wavelengths from about 2.9 μm to 3.1 μm, previously noticed in a 3-μm spectrum obtained by the Infrared Space Observatory (ISO) in 1996. While Brooke et al. (Brooke, T.Y., Knacke, R.F., Encrenaz, T., Drossart, P., Crisp, D., Feuchtgruber, H. [1998]. Icarus 136, 1-13) were able to fit the ISO spectrum very well using ammonia ice as the sole source of particulate absorption, Sromovsky and Fry (Sromovsky, L.A., Fry, P.M. [2010]. Icarus 210, 211-229), using significantly revised NH₃ gas absorption models, showed that ammonium hydrosulfide (NH₄SH) provided a better fit to the ISO spectrum than NH₃, but that the best fit was obtained when both NH₃ and NH₄SH were present in the clouds. Although the large FOV of the ISO instrument precluded identification of the spatial distribution of these two components, the VIMS spectra at low and intermediate phase angles show that 3-μm absorption is present in zones and belts, in every region investigated, and both low- and high-opacity samples are best fit with a combination of NH₄SH and NH₃ particles at all locations. The best fits are obtained with a layer of small ammonia-coated particles (r ∼ 0.3 μm) overlying but often close to an optically thicker but still modest layer of much larger NH₄SH particles (r ∼ 10 μm), with a deeper optically thicker layer, which might also be composed of NH₄SH. Although these fits put NH₃ ice at pressures less than 500 mb, this is not inconsistent with the lack of prominent NH₃ features in Jupiter’s longwave spectrum because the reflectivity of the core particles strongly suppresses the NH₃ absorption features, at both near-IR and thermal wavelengths. Unlike Jupiter, Saturn lacks the broad 3-μm absorption feature, but does exhibit a small absorption near 2.965 μm, which resembles a similar jovian feature and suggests that both planets contain upper tropospheric clouds of sub-micron particles containing ammonia as a minor fraction.     

Regolith depth growth on an icy body orbiting Saturn and evolution of bidirectional reflectance due to surface composition changes

Using a Markov chain model, we consider the regolith growth on a small body in orbit around Saturn, subject to meteoritic bombardment, and assuming all impact ejecta are re-collected. We calculate the growth of regolith and the fractional pollution, assuming an initial pure ice body and amorphous carbon as a pollutant. We extend the meteorite flux of Cuzzi and Estrada (Cuzzi, J., Estrada, P. [1998]. Icarus 132, 1-35) to larger sizes to consider the effect of disruption of the moonlet on other moonlets in the ensemble. This is a relatively small effect, completely negligible for moonlets of 1 m radius. For the given impact model, fractional pollution reaches 22% for 1 m bodies, but only 3% for 10 m bodies, 1.7% for 20 m bodies, and 1% for 30 m bodies after 4 byr. By considering an ensemble of moonlets, which have identical cross-sections for releasing and capturing ejecta, this analysis can be extended to a model of particles in Saturn’s rings, where the calculated spectra can be compared to observed ring spectra. The measured spectral reflectance of Saturn’s rings from Cassini observations therefore constrains the size and age of the ring particles. The comparison between 1 m, 10 m, 20 m, and 30 m particles confirms that for larger ring mass, the current rings would be less polluted; for the largest particles, we expect negligible changes in the UV spectrum after 4 byr of meteoritic bombardment. We consider two end members for mixing of the meteoritic material: areal and intimate. Given the uncertainties in the actual mixing of the meteoritic infall and in its composition (as a worst case, we assume the meteoritic material is 100% amorphous carbon, intimately mixed) initially pure ice 30 m ring particles would darken after 4 byr of exposure by 15%.     

Spectral reflectance properties of carbonaceous chondrites: 1. CI chondrites

Existing reflectance spectra of CI chondrites (18 spectra of 3 CIs) have been augmented with new (18 spectra of 2 CIs) reflectance spectra to ascertain the spectral variability of this meteorite class and provide insights into their spectral properties as a function of grain size, composition, particle packing, and viewing geometry. Particle packing and viewing geometry effects have not previously been examined for CI chondrites. The current analysis is focused on the 0.3-2.5 μm interval, as this region is available for the largest number of CI spectra. Reflectance spectra of powdered CI1 chondrites are uniformly dark (<10% maximum reflectance) but otherwise exhibit a high degree of spectral variability. Overall spectral slopes range from red (increasing reflectance with increasing wavelength) to blue (decreasing reflectance with increasing wavelength). A number of the CI spectra exhibit weak (<5% deep) absorption bands that can be attributed to both phyllosilicates and magnetite. Very weak absorption bands attributable to other CI phases, such as carbonates, sulfates, and organic matter may be present in one or a few spectra, but their identification is not robust. We found that darker spectra are generally correlated with bluer spectral slopes: a behavior most consistent with an increasing abundance of fine-grained magnetite and/or insoluble organic material (IOM), as no other CI opaque phase appears able to produce concurrent darkening and bluing. Magnetite can also explain the presence of an absorption feature near 1 μm in some CI spectra. The most blue-sloped spectra are generally associated with the larger grain size samples. For incidence and emission angles <60°, increasing phase angle results in darker and redder spectra, particularly below ∼1 μm. At high incidence angles (60°), increasing emission angle results in brighter and redder spectra. More densely packed samples and underdense (fluffed) samples show lower overall reflectance than normally packed and flat-surface powdered samples. Some B-class asteroids exhibit selected spectral properties consistent with CI chondrites, although perfect spectral matches have not been found. Because many CI chondrite spectra exhibit absorption features that can be related to specific mineral phases, the search for CI parent bodies can fruitfully be conducted using such parameters.     

Revised vertical cloud structure of Uranus from UKIRT/UIST observations and changes seen during Uranus’ Northern Spring Equinox from 2006 to 2008: Application of new methane absorption data and comparison with Neptune

Long-slit spectroscopy observations of Uranus by the United Kingdom InfraRed Telescope UIST instrument in 2006, 2007 and 2008 have been used to monitor the change in Uranus’ vertical and latitudinal cloud structure through the planet’s Northern Spring Equinox in December 2007.These spectra were analysed and presented by Irwin et al. (Irwin, P.G.J., Teanby, N.A., Davis, G.R. [2009]. Icarus 203, 287-302), but since publication, a new set of methane absorption data has become available (Karkoschka, E., Tomasko, M. [2010]. Methane absorption coefficients for the jovian planets from laboratory, Huygens, and HST data. Icarus 205, 674-694.), which appears to be more reliable at the cold temperatures and high pressures of Uranus’ deep atmosphere. We have fitted k-coefficients to these new methane absorption data and we find that although the latitudinal variation and inter-annual changes reported by Irwin et al. (2009) stand, the new k-data place the main cloud deck at lower pressures (2-3 bars) than derived previously in the H-band of ∼3-4 bars and ∼3 bars compared with ∼6 bars in the J-band. Indeed, we find that using the new k-data it is possible to reproduce satisfactorily the entire observed centre-of-disc Uranus spectrum from 1 to 1.75 μm with a single cloud at 2-3 bars provided that we make the particles more back-scattering at wavelengths less than 1.2 μm by, for example, increasing the assumed single-scattering albedo from 0.75 (assumed in the J and H-bands) to near 1.0. In addition, we find that using a deep methane mole fraction of 4% in combination with the associated warm ‘F’ temperature profile of Lindal et al. (Lindal, G.F., Lyons, J.R., Sweetnam, D.N., Eshleman, V.R., Hinson, D.P. [1987]. J. Geophys. Res. 92, 14987-15001), the retrieved cloud deck using the new (Karkoschka and Tomasko, 2010) methane absorption data moves to between 1 and 2 bars.The same methane absorption data and retrieval algorithm were applied to observations of Neptune made during the same programme and we find that we can again fit the entire 1-1.75 μm centre-of-disc spectrum with a single cloud model, providing that we make the stratospheric haze particles (of much greater opacity than for Uranus) conservatively scattering (i.e. ω = 1) and we also make the deeper cloud particles, again at around the 2 bar level more reflective for wavelengths less than 1.2 μm. Hence, apart from the increased opacity of stratospheric hazes in Neptune’s atmosphere, the deeper cloud structure and cloud composition of Uranus and Neptune would appear to be very similar.     

Spectroscopic survey of X-type asteroids

We present reflected light spectral observations from 0.4 to 2.5 μm of 24 asteroids chosen from the population of asteroids initially classified as Tholen X-type objects (Tholen, 1984). The X complex in the Tholen taxonomy comprises the E, M and P classes which have very different inferred mineralogies but which are spectrally similar to each other, with featureless spectra in visible wavelengths.The data were obtained during several observing runs in the 2004-2007 years at the NTT, TNG and IRTF telescopes. Sixteen asteroids were observed in the visible and near-infrared wavelength range, seven objects in the visible wavelength range only, and one object in the near-infrared wavelength range only. We find a large variety of near-infrared spectral behaviors within the X class, and we identify weak absorption bands in spectra of 11 asteroids. Our spectra, together with albedos published by Tedesco et al. (2002), can be used to suggest new Tholen classifications for these objects. We describe 1 A-type (1122), 1 D-type (1328), 1 E-type (possibly, 3447 Burckhalter), 10 M-types (77, 92, 184, 337, 417, 741, 758, 1124, 1146 and 1355), 5 P-types (275, 463, 522, 909, 1902), and 6 C-types (50, 220, 223, 283, 517, and 536). In order to constrain the possible composition of these asteroids, we perform a least-squares search through the RELAB spectral database. Many of the best fits are consistent with meteorite analogue materials suggested in the published literature. In fact, we find that seven of the new M-types can be fit with metallic iron (or pallasite) materials, and that the low albedo C/P-type asteroids are best fitted with CM meteorites, some of which have been subjected to heating episodes or laser irradiation. Our method of searching for meteorite analogues emphasizes the spectral characteristics of brightness and shape, and de-emphasizes minor absorption bands. Indeed, faint absorption features like the 0.9 μm band seen on four newly classified M-type asteroids are not reproduced by the iron meteorites. In these cases, we have searched for geographical mixture models that can fit the asteroid spectrum, minor bands, and albedo. We find that a few percent (less than 3%) of orthopyroxene added to iron or pallasite meteorite, results in good spectral matches, reproducing the weak spectral feature around 0.9 μm seen on 92 Undina, 417 Suevia, and 1124 Stroobantia. For 337 Devosa, a mixture model that better reproduces its spectral behavior and the 0.9 μm feature is made with Esquel pallasite enriched with goethite (2%).Finally, we consider the sample of the X-type asteroids we have when we combine the present observations with previously published observations for a total of 72 bodies. This sample includes M and E-type asteroid data presented in [Fornasier et al., 2008] and [Fornasier et al., 2010]. We find that the mean visible spectral slopes for the different E, M and P Tholen classes are very similar, as expected. An analysis of the X-type asteroid distribution in the main belt is also reported, following both the Tholen and the Bus-DeMeo taxonomies (DeMeo et al., 2009).     

The near-IR spectrum of Titan modeled with an improved methane line list

We have obtained spatially resolved spectra of Titan in the near-infrared J, H and K bands at a resolving power of ∼5000 using the near-infrared integral field spectrometer (NIFS) on the Gemini North 8 m telescope. Using recent data from the Cassini/Huygens mission on the atmospheric composition and surface and aerosol properties, we develop a multiple-scattering radiative transfer model for the Titan atmosphere. The Titan spectrum at these wavelengths is dominated by absorption due to methane with a series of strong absorption band systems separated by window regions where the surface of Titan can be seen. We use a line-by-line approach to derive the methane absorption coefficients. The methane spectrum is only accurately represented in standard line lists down to ∼2.1 μm. However, by making use of recent laboratory data and modeling of the methane spectrum we are able to construct a new line list that can be used down to 1.3 μm. The new line list allows us to generate spectra that are a good match to the observations at all wavelengths longer than 1.3 μm and allow us to model regions, such as the 1.55 μm window that could not be studied usefully with previous line lists such as HITRAN 2008. We point out the importance of the far-wing line shape of strong methane lines in determining the shape of the methane windows. Line shapes with Lorentzian, and sub-Lorentzian regions are needed to match the shape of the windows, but different shape parameters are needed for the 1.55 μm and 2 μm windows. After the methane lines are modeled our observations are sensitive to additional absorptions, and we use the data in the 1.55 μm region to determine a D/H ratio of 1.77 ± 0.20 × 10⁻⁴, and a CO mixing ratio of 50 ± 11 ppmv. In the 2 μm window we detect absorption features that can be identified with the ν₅ + 3ν₆ and 2ν₃ + 2ν₆ bands of CH₃D.     

Emissivity measurements of analogue materials for the interpretation of data from PFS on Mars Express and MERTIS on Bepi-Colombo

The Planetary Fourier Spectrometer (PFS) onboard the Mars Express Mission provides thermal infrared, hyperspectral images of Mars and in the future the Mercury Radiometer and Thermal Infrared Spectrometer (MERTIS), part of the selected payload for the Bepi-Colombo Mission, will collect analogous data for Mercury. To interpret these remote sensing data it is essential to understand the spectral emittance of planetary analogue materials and a spectral library of emissivity measurements is needed. Here we introduce the emissivity device built at DLR (Berlin). The device is coupled to a Fourier transform infrared spectrometer (Bruker IFS 88), purged with dry air and equipped with a cooled MCT-detector. We discuss theoretical background of our thermal emission measurements and describe our standard experimental procedures, which are being used to create the Berlin emissivity database (BED). This study presents and discuss the 6.3-22 μm thermal emission spectra of fine-grained feldspar separates ranging from <25 to 90-125 μm. We discuss diagnostic potential of the features present in the emission spectra of plagioclase and alkali feldspars and the particle size effects.     

New laboratory measurements of CH4 in Titan's conditions and a reanalysis of the DISR near-surface spectra at the Huygens landing site

Laboratory spectra of methane-nitrogen mixtures have been recorded in the near-infrared range (1.0-1.65 μm) in conditions similar to Titan's near surface, to facilitate the interpretation of the DISR/DLIS (DISR—Descent Imager/Spectral Radiometer) spectra taken during the last phase of the descent of the Huygens Probe, when the surface was illuminated by a surface-science lamp. We used a 0.03 cm⁻¹ spectral resolution, adequate to resolve the lines at high pressure (p_N2∼1.5 bar). By comparing the laboratory spectra with synthetic calculations in the well-studied ν₂+2ν₃ band (7515-7620 cm⁻¹), we determine a methane absorption column density of 178±20 cm atm and a temperature of 118±10 K in our experiment. From this, we derive the methane absorption coefficients over 1.0-1.65 μm with a 0.03 cm⁻¹ sampling, allowing for the extrapolation of the results to any other methane column density under the relevant pressure and temperature conditions. We then revisit the calibration and analysis of the Titan “lamp-on” DLIS spectra. We infer a 5.1±0.8% methane-mixing ratio in the first 25 m of Titan's atmosphere. The CH₄ mixing ratio measured 90 s after landing from a distance of 45 cm is found to be 0.92±0.25 times this value, thus showing no post-landing outgassing of methane in excess of ∼20%. Finally, we determine the surface reflectivity as seen between 25 m and 45 cm and find that the 1500 nm absorption band is deeper in the post-landing spectrum as compared to pre-landing.