Component-resolved near-infrared spectra of the (22) Kalliope system

We observed (22) Kalliope and its companion Linus with the integral-field spectrograph OSIRIS, which is coupled to the adaptive optics system at the W.M. Keck 2 telescope on March 25, 2008. We present, for the first time, component-resolved spectra acquired simultaneously in each of the Zbb (1-1.18 μm), Jbb (1.18-1.42 μm), Hbb (1.47-1.80 μm), and Kbb (1.97-2.38 μm) bands. The spectra of the two bodies are remarkably similar and imply that both bodies were formed at the same time from the same material; such as via incomplete re-accretion after a major impact on the precursor body.     

Spatial and short-term temporal variations in Uranus’ near-infrared spectrum

We obtained near-infrared spectra of Uranus at NASA’s Infrared Telescope Facility during the planet’s September 2006 and September 2007 oppositions. Ratios between the spectra indicate that in 2006, Uranus’ methane windows appeared much brighter in the south than in the north, and that between 2006 and 2007 they grew dimmer in the south and brighter in the north; we interpret these variations to be primarily caused by changing brightness in Uranus’ upper cloud layer near 2 bars.     

First observation of CO at 345 GHz in the atmosphere of Saturn with the JCMT: New constraints on its origin

We have performed the first observation of the CO(3-2) spectral line in the atmosphere of Saturn with the James Clerk Maxwell Telescope. We have used a transport model of the atmosphere of Saturn to constrain the origin of the observed CO. The CO line is best-fit when the CO is located at pressures less than (15±2) mbar with a mixing ratio of (2.5±0.6)×10^-8 implying an external origin. By modeling the transport in Saturn’s atmosphere, we find that a cometary impact origin with an impact 200-350 years ago is more likely than continuous deposition by interplanetary dust particles (IDP) or local sources (rings/satellites). This result would confirm that comet impacts are relatively frequent and efficient providers of CO to the atmospheres of the outer planets. However, a diffuse and/or local source cannot be rejected, because we did not account for photochemistry of oxygen compounds. Finally, we have derived an upper limit of ∼1×10^-9 on the tropospheric CO mixing ratio.     

Observations of CO in the atmosphere of Mars with PFS onboard Mars Express

We have analyzed spectra of CO recorded with the instrument PFS onboard Mars Express in the (1-0) band. The dataset we used ranges in time from January until June 2004 (L_S=331^°.17 until L_S=51^°.61; end of Mars Year 26, beginning of Mars Year 27). The aim of this work was to determine the amplitude of the CO mixing ratio departures from the mean globally averaged value currently admitted (8±3×10^-4) [Kaplan, L.D., Connes, J., Connes, P., 1969. Carbon monoxide in the martian atmosphere. Astron. J. 157, L187-L192] as a function of season, local time and location on the planet. We therefore processed the data from 90 calibrated orbits. The globally averaged CO mixing ratio value we derive from our dataset, 11.1×10^-4, is compatible with the range found by Kaplan et al. [1969. Carbon monoxide in the martian atmosphere. Astron. J. 157, L187-L192], although somewhat higher than the “standard” value. However, the CO mixing ratio we retrieve exhibits large variations (roughly between 3×10^-4 and 18×10^-4). Such relative variations have been used on a statistical basis to derive main trends as a function of latitude for three L_S ranges: 331-360^°, 0-30^° and 30-52^°. For the first L_S range, we seem to have an enhancement of the CO mixing ratio towards the northern latitudes, probably linked to the CO₂ condensation in winter on the north polar cap. The situation for the two other L_S ranges is not so clear, mainly as we lack data on the southern hemisphere. We roughly agree with the work of Krasnopolsky [2007. Long-term spectroscopic observations of Mars using IRTF/CSHELL: mapping of O2 dayglow, CO and search for CH4. Icarus 190, 93-102] for L_S=331-360^°, thus confirming the effect of seasonal condensation of CO₂ on the north polar cap, but we have no agreement for other seasons.     

Detecting protoplanets with ALMA

Theoretical investigations show that planet-disk interactions cause structures in circumstellar disks, which are usually much larger in size than the planet itself and thus more easily detectable. The specific result of planet-disk interactions depends on the evolutionary stage of the disk. Exemplary signatures of planets embedded in disks are gaps and spiral density waves in the case of young, gas-rich protoplanetary disks and characteristic asymmetric density patterns in debris disks. Numerical simulations convincingly demonstrate that high-resolution imaging performed with observational facilities which are already available or will become available in the near future will allow to trace these “fingerprints” of planets in protoplanetary and debris disks. These observations will provide a deep insight into specific phases of the formation and early evolution of planets in circumstellar disks. In this context, the Atacama Large Millimeter Array (ALMA) will play a crucial role by allowing to trace features in disks which are indicative for various stages of the formation and early evolution of planets in circumstellar disks.     

Ultraviolet observations of Phoebe from the Cassini UVIS

Observations of Saturn's distant moon Phoebe were made at far-ultraviolet (FUV) (1100-1900 Å) and extreme-ultraviolet (EUV) (600-1100 Å) wavelengths by the Cassini Ultraviolet Imaging Spectrograph (UVIS) during the Cassini spacecraft flyby on June 11, 2004. These are the first UV spectra of Phoebe and the first detection of water ice on a Solar System surface using FUV wavelengths. The characteristics of water ice in the FUV are presented, and Hapke models are used to interpret the spectra in terms of composition and grain size; the use of both areal and intimate mixing models is explored. Non-ice species used in these models include carbon, ice tholin, Triton tholin, poly-HCN and kerogen. Satisfactory disk-integrated fits are obtained for intimate mixtures of ∼10% H₂O plus a non-ice species. Spatially resolved regions of higher (∼20%) and lower (∼5%) H₂O ice concentrations are also detected. Phoebe does not display any evidence of volatile activity. Upper limits on atomic oxygen and carbon are 5×¹⁰¹¹ and 2×¹⁰¹² atoms/cm², respectively, for solar photon scattering. The UVIS detection of water ice on Phoebe, and the ice amounts detected, are consistent with IR measurements and contribute to the evidence for a Phoebe origin in the outer Solar System rather than in the main asteroid belt.     

Global-scale near infrared variability on Mars: Analysis of 2003 Mars opposition observations from HST/NICMOS

We have used HST/NICMOS to observe approximately 57% of the martian surface in 7 narrow band filters (0.97, 1.08, 1.13, 1.66, 1.90, 2.12, and 2.15 μm) during the 2003 opposition (Ls∼250°) and at a resolution of ∼12 km/pixel. Principal components analysis (PCA) of the dataset has identified regional variability on scales of hundreds of kilometers associated with differences in the near-infrared spectrum of Mars. Visualization of the data in principal component space has allowed us to identify spectral endmembers associated with the south polar cap, the classic bright terrains, northern Syrtis Major, southern Syrtis Major, Tyrrhena Terra, and Acidalia Planitia. The two Syrtis Major endmembers and the Tyrrhena Terra endmember differ in their absolute reflectivities but have the same spectral shape at wavelengths longer than 1.6 μm. The Acidalia endmember is distinct from the other dark terrain endmembers because it exhibits a strong negative near-IR spectral slope. Comparisons with spectral library measurements cannot provide unique constraints on the surface mineralogy for these sparsely-sampled spectral data. However, the observed spectral variations between Tyrrhena Terra and Syrtis Major are consistent with variations in iron- and sulfur-bearing minerals, and the relatively strong negative spectral slope in the spectrum of Acidalia is consistent with the presence of hydrated alteration products. Additional comparison with previous NICMOS observations taken in 1997 at Ls∼150° indicate that the average near-IR spectral slope of the Acidalia region is more negative during the late northern fall than during the mid northern summer. This may indicate seasonal variations in the presence of either adsorbed water or re-hydrated minerals in the regolith of Acidalia.     

Infrared studies at the ice laboratory of Alcoy

At present, there are few laboratory spectra of analogs of astrophysical interest in the far-infrared range (FIR). Laboratory infrared (IR) spectra of simple ices and its mixtures obtained at low temperature and pressure are found mainly up to 25 μm, and few up to 200 μm. On the other hand, there are some spectra for carbonaceous material and silicates up to 2000 μm. Our laboratory is equipped with an IR spectrometer that integrates a Michelson interferometer with a resolution better than 0.25 cm⁻¹ and that operates under vacuum conditions of 10⁻¹ mbar. There is also a silicon bolometer, a very high-sensitivity detector in comparison with the standard deuterated triglycine sulfate (DTGS) detectors. The use of the bolometer and the possibility of working under vacuum conditions inside the optics and the sample compartment of the spectrometer allow obtaining high-sensitivity spectra free from H₂O vapor and CO₂ gas bands. Those conditions are necessary to obtain high-quality spectra in the FIR where absorption bands are much less intense than those in the mid-IR region. In our laboratory there is also a high-vacuum chamber that allows different studies on ices deposited onto a cold finger. We have already carried out experiments on the study of ice density as a function of temperature, UV irradiation of ices, temperature-programmed desorption (TPD) and UV-vis reflectance. In this work, we present the design of the experimental setup we are building to carry out different experiments simultaneously on the same ice sample, including spectra measurements in the mid-IR range (MIR) and the FIR. This design integrates jointly the IR spectrometer, the high-vacuum chamber and the silicon bolometer. Lastly, we show a spectrum we have obtained of a solid of astrophysical interest such as crystalline forsterite grains by using the polyethylene pellet technique.     

S2O, polysulfuroxide and sulfur polymer on Io's surface?

To settle the question of disulfur monoxide and sulfur monoxide deposition and occurrence on Io's surface, we performed series of laboratory experiments reproducing the condensation of S₂O at low temperature. Its polymerization has been monitored by recording infrared spectra under conditions of temperature, pressure, mixing with SO₂ and UV-visible radiation simulating that of Io's surface. Our experiments show that S₂O condensates are not chemically stable under ionian conditions. We also demonstrate that SO and S₂O outgassed by Io's volcanoes and condensing on Io's surface should lead to yellow polysulfuroxide deposits or to white deposits of S₂O diluted in sulfur dioxide frost (i.e., S₂O/SO₂ < 0.1%). Thus S₂O condensation cannot be responsible for the red volcanic deposits on Io. Comparison of the laboratory infrared spectra of S₂O and polysulfuroxide with NIMS/Galileo infrared spectra of Io's surface leads us to discuss the possible identification of polysulfuroxide. We also recorded the visible transmission spectra of sulfur samples resulting from polysulfuroxide decomposition. These samples consist in a mixture of sulfur polymer and orthorhombic sulfur. Using the optical constants extracted from these measurements, we show that a linear combination of the reflectance spectra of our samples, the reflectance spectrum of orthorhombic S₈ sulfur and SO₂ reflectance spectrum, leads to a very good matching of Io's visible spectrum between 330 and 520 nm. We conclude then that Io's surface is probably mainly composed of sulfur dioxide and a mixture of sulfur S₈ and sulfur polymer. Some polysulfuroxide could also co-exist with these dominant components, but is probably restricted to some volcanic areas.     

Generation and performance of automated jarosite mineral detectors for visible/near-infrared spectrometers at Mars

We have developed two automated detectors that can recognize the sulfate mineral jarosite in unknown visible to near-infrared spectra (350-2500 nm). The two detectors are optimized for use within the terrestrial and martian atmospheres. The detectors are built from Support Vector Machines trained using a generative model to create linear mixtures of library mineral spectra. Both detectors performed with an average ∼90% accuracy on laboratory spectra of single minerals and the laboratory and field spectra of rocks collected in a hydrothermal environment. This type of algorithm will contribute to the efficiency of onboard data analysis of landed and orbital visible/near-infrared spectrometers at Mars.