Hemispherical distribution of CO above the Venus’ clouds by ground-based 2.3 μm spectroscopy

The abundance of carbon monoxide in the Venus’ dayside atmosphere above the clouds was measured by ground-based 2.3 μm spectroscopy for 4 days. The hemispherical distributions found show no significant latitudinal or longitudinal structure. The disc-averaged mixing ratio of 58 ± 17 ppm found at a representative height of 62-67 km is consistent with previous measurements. Such a flat distribution of CO abundance above the clouds seems to be controlled by an efficient horizontal eddy diffusion with a time scale of 30 days or shorter although the CO distribution below the clouds seems to be controlled by the meridional circulation. The pole-ward wind speed of the meridional circulation above the clouds is estimated to be 0.2 m s⁻¹ or less based on the difference between the CO mixing ratios above and below the clouds.     

Hemispheric distributions of HCl above and below the Venus’ clouds by ground-based 1.7 μm spectroscopy

The abundance of hydrogen chloride (HCl) in the Venus atmosphere was measured by ground-based IR spectroscopy. The dayside measurements were performed in May 2007 with a resolution of 40,000, and the nightside measurements in October 1999 with a resolution of 1000. The hemispheric distributions of the HCl mixing ratio measured above the Venus’ clouds show no significant structure with a disc-averaged value of 0.74±0.06 ppm which is in the similar range as the previous report of 0.6±0.2 ppm. The representative height for the dayside measurements is estimated to be 60-66 km. Recent results by Venus Express/SPICAV/SOIR show much smaller values of 0.1-0.2 ppm at 64-94 km; however the direct comparison is difficult due to the different spatial conditions. The hemispheric distributions of the ³⁵Cl/³⁷Cl isotope ratio are also found to show no significant structure with a disc-averaged value of 3.1±0.4 which coincides with the terrestrial value of 3.1. The HCl mixing ratios below the clouds are also found to show no significant structure with a disc-averaged value of 0.40±0.05 ppm, which is similar to the previous reports of 0.4-0.5 ppm. The larger HCl mixing ratio above the clouds than below suggests the production of HCl in the cloud region or above. Also, a uniform hemispherical distribution of H₂O is found below the clouds with a disc-averaged mixing ratio of 25±5 ppm; this is in the same range as the previous measurements. Those uniform distributions of HCl and H₂O support the fact that their chemical lifetimes are much longer than that of mixing as has been discussed so far.     

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.     

Vertical profiling of SO2 and SO above Venus’ clouds by SPICAV/SOIR solar occultations

New measurements of sulfur dioxide (SO₂) and monoxide (SO) in the atmosphere of Venus by SPICAV/SOIR instrument onboard Venus Express orbiter provide ample statistics to study the behavior of these gases above Venus’ clouds. The instrument (a set of three spectrometers) is capable to sound atmospheric structure above the clouds in several observation modes (nadir, solar and stellar occultations) either in the UV or in the near IR spectral ranges. We present the results from solar occultations in the absorption ranges of SO₂ (190–230 nm, and at 4 μm) and SO (190–230 nm). The dioxide was detected by the SOIR spectrometer at the altitudes of 65–80 km in the IR and by the SPICAV spectrometer at 85–105 km in the UV. The monoxide’s absorption was measured only by SPICAV at 85–105 km. We analyzed 39 sessions of solar occultation, where boresights of both spectrometers are oriented identically, to provide complete vertical profiling of SO₂ of the Venus’ mesosphere (65–105 km). Here we report the first firm detection and measurements of two SO₂ layers. In the lower layer SO₂ mixing ratio is within 0.02–0.5 ppmv. The upper layer, also conceivable from microwave measurements by Sandor et al. (Sandor, B.J., Todd Clancy, R., Moriarty-Schieven, G., Mills, F.P. [2010]. Icarus 208, 49–60) is characterized by SO₂ increasing with the altitude from 0.05 to 2 ppmv, and the [SO₂]/[SO] ratio varying from 1 to 5. The presence of the high-altitude SO_x species could be explained by H₂SO₄ photodissociation under somewhat warmer temperature conditions in Venus mesosphere. At 90–100 km the content of the sulfur dioxide correlates with temperature increasing from 0.1 ppmv at 165–170 K to 0.5–1 ppmv at 190–192 K. It supports the hypothesis of SO₂ production by the evaporation of H₂SO₄ from droplets and its subsequent photolysis at around 100 km.     

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.     

The 1.10- and 1.18-μm nightside windows of Venus observed by SPICAV-IR aboard Venus Express

Observations of the 1.10- and 1.18-μm nightside windows by the SPICAV-IR instrument aboard Venus Express were analyzed to characterize the various sources of gaseous opacity and determine the H₂O mole fraction in the lower atmosphere of Venus. We showed that the line profile model of Afanasenko and Rodin (Afanasenko, T.S., Rodin, A.V. [2007]. Astron. Lett. 33, 203–210) underestimates the CO₂ absorption in the high-wavelength wing of the 1.18-μm window and we derived an empirical lineshape that matches this wing well. An additional continuum opacity is required to reproduce the variation of the 1.10- and 1.18-μm radiances with surface elevation as observed by the VIRTIS-M instrument aboard Venus Express. A constant absorption coefficient of 0.7 ± 0.2 × 10⁻⁹ cm⁻¹ am⁻² best reproduces the observed variation. We compared spectra calculated with different CO₂ and H₂O line lists. We found that the CDSD line list lacks the 5ν₁ + ν₃ series of CO₂ bands, which provide significant opacity in Venus’ deep atmosphere, and we have constructed a composite line list that best reproduces the observations. We also showed for the first time that HDO brings significant absorption at 1140–1190 nm. Using the best representation of the atmospheric opacity we could reach, we retrieved a water vapor mole fraction of ppmv, pertaining to the altitude range 5–25 km. Combined with previous measurements in the 1.74- and 2.3-μm windows, this result provides strong evidence for a uniform H₂O profile below 40 km, in agreement with chemical models.     

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).     

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.     

High resolution investigation of the 7 μm region of the ethane spectrum

Building upon previous studies, we re-investigated the ethane spectrum between 1330 and 1610 cm^?1 by combining unapodized spectra obtained at room temperature with a Bruker Fourier transform spectrometer (FTS) in Brussels and at 131 K with a Bruker FTS in Pasadena. The maximum optical path differences (MOPD) of the two datasets were 450 and 323.7 cm, corresponding to spectral resolutions of 0.0020 and 0.0028 cm^?1, respectively. Of the 15,000 lines observed, over 4592 transitions were assigned to the ν₆ (at 1379 cm^?1), ν₈ (at 1472 cm^?1), ν₄+ν₁₂ (at 1481 cm^?1) and 2ν₄+ν₉ (at 1388 cm^?1) bands, and another 1044 transitions were located for the ν₄+ν₈?ν₄ hot band (at 1472 cm^?1). Our new analysis included an improved implementation of the Hamiltonian calculation needed to interpret the complex spectral structures caused by numerous interactions affecting these four modes of vibration. From these results, we created the first line-by-line database containing the molecular parameters for over 20,000 ¹²C₂H₆ transitions at 7 μm.     

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.     

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 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.     

Optical constants of Titan tholins at mid-infrared wavelengths (2.5–25 μm) and the possible chemical nature of Titan’s haze particles

Complex organic materials may exist as haze layers in the atmosphere of Titan and as dark coloring agents on icy satellite surfaces. Laboratory measurements of optical constants of plausible complex organic materials are necessary for quantitative evaluation from remote sensing observations, and to document the existence of complex organic materials in the extraterrestrial environments. The recent Cassini VIMS and CIRS observations provide new constraints on Titan’s haze properties in the mid-infrared wavelength region. Here, we present the optical constants (2.5–25 μm) of Titan tholins generated with cold plasma irradiation of a N₂/CH₄ (90/10) gas mixture at pressures of 0.26 mbar, 1.6 mbar, and 23 mbar. Our new optical constants of three types of Titan tholins suggest that no single Titan tholin in this study fulfills all the observational constraints of the Titan haze material. The discrepancy remains a challenge for future modeling and laboratory efforts that aim toward a better understanding of Titan’s haze material.     

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.     

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.     

The distribution of Titan's high-altitude (out to ∼50,000 km) exosphere from energetic neutral atom (ENA) measurements by Cassini/INCA

We report observations of Titan's high-altitude exosphere detected out to about 50,000 km altitude. The observations were made by the Ion Neutral Camera (INCA) on board the Cassini spacecraft. INCA detects energetic neutral atoms (ENA) that are formed when the ambient magnetospheric ions charge exchange with Titan's neutral atmosphere and exosphere. We find that Titan's exospheric H₂ distribution follows closely a full Chamberlain distribution including ballistic, escaping and satellite distributions. As expected, neutral densities are dominated by a satellite distribution above about 10,000 km. The maximum detectable extent of the exosphere (～50,000 km) coincides with the radius of the Hill sphere of gravitational influence from Saturn. While we find no direct indications of a neutral Titan torus with densities greater than about 1000 cm^?3, we observe interesting asymmetries in the distribution that warrants further investigation. Based on these findings we compute the average precipitating ENA flux to be about 5×10⁶ keV/(cm² s), or 8×10^?3 erg/(cm² s), which is directly comparable to that of precipitating energetic ions (Sittler, et al., 2009) and slightly higher than that of solar EUV (Tobiska, 2004). Thus, the energy deposited by precipitating ENAs must also be taken into consideration when studying the energy balance of Titan's thermosphere.     

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.