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.     

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.     

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 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.     

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.     

Direct wind measurements from November 2007 in Venus’ upper atmosphere using ground-based heterodyne spectroscopy of CO2 at 10 μm wavelength

Between November 23 and 28, 2007, the Cologne Tuneable Heterodyne Infrared Spectrometer THIS was installed at the McMath-Pierce Solar Telescope (Kitt Peak, Arizona, USA) to determine zonal wind velocities and to estimate the subsolar-to-antisolar flow. We investigate dynamics in the upper atmosphere of Venus by measuring the Doppler shift of fully-resolved non-LTE CO₂ emission lines at 959.3917 cm^?1 (10.423 μm), which probe a narrow altitude region in Venus’ atmosphere around 110 ± 10 km (～1 μbar). The results show no significant zonal wind velocity at the equator. An increase with latitude up to 43 ± 13 m/s at a latitude of 33°N was observed. This confirms the deduction of a minor influence of Venus superrotation at an altitude of 110 km from previous measurements in May 2007 (Sornig et al., 2008). The specific observing geometry enables estimating the maximum cross terminator velocity of the subsolar-to-antisolar flow at 72 ± 47 m/s.     

Temperature and pressure determinations in the Venus atmosphere by means of high-resolution spectra from 1 to 2.5 μm

Twenty-one bands of CO₂ and the 2-0 band of CO were analyzed for best temperature and pressure fits from Venus spectra obtained with the “Connes” interferometer at the Steward Observatory 2.25-m telescope during the spring of 1971. An average temperature of 241 ± 7°K, an effective pressure of 0.12 ± 0.06 atm, and an average two-way transmission abundance of 3 km-amagat were determined. No difference in temperature or pressure between hot bands, a double hot band, and regular bands was found. Our results were compared to model calculations for a reflecting layer and scattering atmosphere. The results indicate that, most likely, spectroscopic line formation occurs in a relatively clear space above a scattering cloud layer with a reasonably well-defined upper boundary.     

Mineralogy and thermal properties of V-type Asteroid 956 Elisa: Evidence for diogenitic material from the Spitzer IRS (5-35 μm) spectrum

We present the thermal infrared (5-35 μm) spectrum of 956 Elisa as measured by the Spitzer Infrared Spectrograph (“IRS”; Houck, J.R. et al. [2004]. Astrophys. J. Suppl. 154, 18-24) together with new groundbased lightcurve data and near-IR spectra. From the visible lightcurve photometry, we determine a rotation period of 16.494 ± 0.001 h, identify the rotational phase of the Spitzer observations, and estimate the visible absolute magnitude (H_V) at that rotational phase to be 12.58 ± 0.04. From radiometric analysis of the thermal flux spectrum, we find that at the time of observation 956 Elisa had a projected radius of 5.3 ± 0.4 km with a visible albedo p_V = 0.142 ± 0.022, significantly lower than that of the prototype V-type asteroid, 4 Vesta. (This corresponds to a radius of 5.2 ± 0.4 km at lightcurve mean.) Analysis with the standard thermal model (STM) results in a sub-solar temperature of 292.3 ±  2.8 K and beaming parameter η = 1.16 ± 0.05. Thermophysical modeling places a lower limit of on the thermal inertia of the asteroid’s surface layer (if the surface is very smooth) but more likely values fall between 30 and depending on the sense of rotation.The emissivity spectrum, calculated by dividing the measured thermal flux spectrum by the modeled thermal continuum, exhibits mineralogically interpretable spectral features within the 9-12 μm reststrahlen band, the 15-16.5 μm Si-O-Si stretching region, and the 16-25 μm reststrahlen region that are consistent with pyroxene of diogenitic composition: extant diogenitic pyroxenes fall within the narrow compositional range Wo_2±1En_74±2Fs_24±1. Spectral deconvolution of the 9-12 μm reststrahlen features indicates that up to ≈20% olivine may also be present, suggesting an olivine-diogenite-like mineralogy. The mid-IR spectrum is inconsistent with non-cumulate eucrite as the major component on the surface of 956 Elisa, although cumulate eucrite material may be present at abundances lower than that of the diogenite component.Analysis of new near-IR spectra of 956 Elisa with the Modified Gaussian Model (MGM; Sunshine, J.M., Pieters, C.M., Pratt, S.F. [1990]. J. Geophys. Res. 95 (May), 6955-6966) results in two pyroxene compositions: 75% magnesian low-Ca pyroxene and 25% high-Ca pyroxene. High-Ca pyroxene is not evident in the mid-IR data, but may belong to a component that is underrepresented in the mid-IR spectrum either because of its spatial distribution on the asteroid or because of its particle size. High-Ca pyroxenes that occur as exsolution lamellae may also be more evident spectrally in the NIR than in the mid-IR. In any case, we find that the mid-IR spectrum of 956 Elisa is dominated by emission from material of diogenite-like composition, which has very rarely been observed among asteroids.     

The 12C/13C and 16O/18O ratios in the atmosphere of Venus from high-resolution 10-μm spectroscopy

Spectra of Venus in the 925- to 980-cm⁻¹ spectral range were recorded in January 1985 at a resolution of 0.06 cm⁻¹. Several lines from the ν₃−ν₁ bands of ¹³CO₂ and ¹²C¹⁶O¹⁸O were observed for the first time. Synthetic spectra, which include absorption from CO₂ bands and from sulfuric acid clouds, are compared to the observations. Taking into account measurement noise as well as systematic errors, the analysis yields ¹²C/¹³C=86±12 and ¹⁶O/¹⁸O=500±80, in agreement with the terrestrial ratios. The results are consistent with previous ground-based near-infrared studies and with in situ mass spectrometer measurements.     

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).     

The 63 μm radiation field in the earth's thermosphere and its influence on the atomic hydrogen temperature

The thermal escape of hydrogen from the Earth's atmosphere is strongly affected by its temperature at the exobase. It has been suggested recently that the hydrogen temperature might be significantly lower than the thermospheric temperature as a result of a collisional exchange of energy with atomic oxygen. The tendency is to cool the hydrogen since the energy of the excited ${}^3\text{P}{}_1$ level of oxygen can be lost from the atmosphere via magnetic dipole emission of the 63 μm line (${}^3\text{P}{}_2\text{?}{}^3\text{P}{}_1$). We present here a detailed calculation of the net cooling effect as a function of altitude throughout the thermosphere. The calculations have been performed for both day and night conditions and for periods of maximum and minimum solar activity conditions. It is found that its effect on ΔT/T varies from a very small value to a maximum of ～3%. We also provide the theoretical framework for describing deviations of the 63 μm emission from local thermodynamic equilibrium and show that these effects can cause the emission to be reduced by as much as 40% near 500 km.