Laboratory measurements of the Ka-band (7.5 mm to 9.2 mm) opacity of phosphine (PH3) and ammonia (NH3) under simulated conditions for the Cassini-Saturn encounter

Recently, a model for the centimeter-wavelength opacity of PH₃ under conditions characteristic of the outer planets was developed by Hoffman et al. (2001, PhD thesis), based on centimeter wavelength laboratory measurements. New laboratory measurements have been conducted which show that this model is also accurate at low pressures and temperatures, and at millimeter wavelengths such as will be employed in Cassini Ka-band (9.3 mm) radio occultation studies. The opacity of PH₃ in a hydrogen/helium (H₂/He) atmosphere has been measured at frequencies in the Ka-band region at 32.7 GHz (9.2 mm), 35.6 GHz (8.4 mm), 37.7 GHz (8.0 mm), and 39.9 GHz (7.5 mm) at pressures of 0.5, 1, and 2 bar and at temperatures of 295, 209, and 188 K. Additionally, new high-precision laboratory measurements of the opacity of NH₃ in an H₂/He atmosphere have been conducted under the same temperature and pressure conditions described for PH₃. These new measurements better constrain the NH₃ opacity model supporting use of a Ben-Reuven lineshape model. These measurements will also elucidate the interpretation of millimeter wavelength observations conducted with the NRAO/VLA at 43 GHz (7 mm).     

In search of water vapor on Jupiter: Laboratory measurements of the microwave properties of water vapor under simulated jovian conditions

Detection and measurement of atmospheric water vapor in the deep jovian atmosphere using microwave radiometry has been discussed extensively by Janssen et al. (Janssen, M.A., Hofstadter, M.D., Gulkis, S., Ingersoll, A.P., Allison, M., Bolton, S.J., Levin, S.M., Kamp, L.W. [2005]. Icarus 173 (2), 447-453.) and de Pater et al. (de Pater, I., Deboer, D., Marley, M., Freedman, R., Young, R. [2005]. Icarus 173 (2), 425-447). The NASA Juno mission will include a six-channel microwave radiometer system (MWR) operating in the 1.3-50 cm wavelength range in order to retrieve water vapor abundances from the microwave signature of Jupiter (see, e.g., Matousek, S. [2005]. The Juno new frontiers mission. Tech. Rep. IAC-05-A3.2.A.04, California Institute of Technology). In order to accurately interpret data from such observations, nearly 2000 laboratory measurements of the microwave opacity of H₂O vapor in a H₂/He atmosphere have been conducted in the 5-21 cm wavelength range (1.4-6 GHz) at pressures from 30 mbars to 101 bars and at temperatures from 330 to 525 K. The mole fraction of H₂O (at maximum pressure) ranged from 0.19% to 3.6% with some additional measurements of pure H₂O. These results have enabled development of the first model for the opacity of gaseous H₂O in a H₂/He atmosphere under jovian conditions developed from actual laboratory data. The new model is based on a terrestrial model of Rosenkranz et al. (Rosenkranz, P.W. [1998]. Radio Science 33, 919-928), with substantial modifications to reflect the effects of jovian conditions. The new model for water vapor opacity dramatically outperforms previous models and will provide reliable results for temperatures from 300 to 525 K, at pressures up to 100 bars and at frequencies up to 6 GHz. These results will significantly reduce the uncertainties in the retrieval of jovian atmospheric water vapor abundances from the microwave radiometric measurements from the upcoming NASA Juno mission, as well as provide a clearer understanding of the role deep atmospheric water vapor may play in the decimeter-wavelength spectrum of Saturn.     

Modeling Jupiter's cloud bands and decks: 2. Distribution and motion of condensates

A simple jovian cloud scheme has been developed for the Oxford Planetary Unified model System (OPUS). NH₃-ice, NH₄SH-solid, H₂O-ice and H₂O-liquid clouds have been modeled in Southern hemisphere limited area simulations of Jupiter. We found that either three or four of the condensates existed in the model. For a deep atmospheric water abundance close to solar composition, an NH₃-ice deck above 0.7 bar, an NH₄SH-solid deck above 2.5 bar and a H₂O-liquid deck with a base at about 7.5 bar and frozen cloud tops formed. If a depleted deep water abundance is assumed, however, a very compact cloud structure develops, where an H₂O-ice cloud forms by direct sublimation above 3 bar. The condensates constitute good tracers of atmospheric motion, and we have confirmed that zonal velocities determined from manual feature tracking in the modeled cloud layers agree reasonably well with the modeled zonal velocities. Dense and elevated clouds form over latitudes with strong atmospheric upwelling and depleted clouds exist over areas with strong downwelling. In the NH₃-ice deck this leads to elevated cloud bands over the zones in the domain and thin clouds over the belts, which is consistent with the observationally deduced distribution. Due to changes in the vertical velocity pattern in the deeper atmosphere, the NH₄SH-solid and water cloud decks are more uniform. This modeled cloud structure thus includes the possibility of more frequent water cloud observations in belts, as this deeper deck could be more easily detected under areas with thin NH₃-ice clouds. Large scale vortices appeared spontaneously in the model and were characterized by elevated NH₃-ice clouds, as expected from observations. These eddies leave the most discernible imprint on the lighter condensate particles of the uppermost layer.     

Updated Galileo probe mass spectrometer measurements of carbon, oxygen, nitrogen, and sulfur on Jupiter

The in situ measurements of the Galileo Probe Mass Spectrometer (GPMS) were expected to constrain the abundances of the cloud-forming condensible volatile gases: H₂O, H₂S, and NH₃. However, since the probe entry site (PES) was an unusually dry meteorological system—a 5-μm hotspot—the measured condensible volatile abundances did not follow the canonical condensation-limited vertical profiles of equilibrium cloud condensation models (ECCMs) such as Weidenschilling and Lewis (1973, Icarus 20, 465-476). Instead, the mixing ratios of H₂S and NH₃ increased with depth, finally reaching well-mixed equilibration levels at pressures far greater than the lifting condensation levels, whereas the mixing ratio of H₂O in the deep well-mixed atmosphere could not be measured. The deep NH₃ mixing ratio (with respect to H₂) of (6.64±2.54)×10⁻⁴ from 8.9-11.7 bar GPMS data is consistent with the NH₃ profile from probe-to-orbiter signal attenuation (Folkner et al., 1998, J. Geophys. Res. 103, 22847-22856), which had an equilibration level of about 8 bar. The GPMS deep atmosphere H₂S mixing ratio of (8.9±2.1)×10⁻⁵ is the only measurement of Jupiter's sulfur abundance, with a PES equilibration level somewhere between 12 and 15.5 bar. The deepest water mixing ratio measurement is (4.9±1.6)×10⁻⁴ (corresponding to only about 30% of the solar abundance) at 17.6-20.9 bar, a value that is probably much smaller than Jupiter's bulk water abundance. The ¹⁵N/¹⁴N ratio in jovian NH₃ was measured at (2.3±0.3)×10⁻³ and may provide the best estimate of the protosolar nitrogen isotopic ratio. The GPMS methane mixing ratio is (2.37±0.57)×10⁻³; although methane does not condense on Jupiter, we include its updated analysis in this report because like the condensible volatiles, it was presumably brought to Jupiter in icy planetesimals. Our detailed discussion of calibration and error analysis supplements previously reported GPMS measurements of condensible volatile mixing ratios (Niemann et al., 1998, J. Geophys. Res. 103, 22831-22846; Atreya et al., 1999, Planet. Space Sci. 47, 1243-1262; Atreya et al., 2003, Planet. Space Sci. 51, 105-112) and the nitrogen isotopic ratio (Owen et al., 2001b, Astrophys. J. Lett. 553, L77-L79). The approximately three times solar abundance of NH₃ (along with CH₄ and H₂S) is consistent with enrichment of Jupiter's atmosphere by icy planetesimals formed at temperatures <40 K (Owen et al., 1999, Nature 402 (6759), 269-270), but would imply that H₂O should be at least 3×solar as well. An alternate model, using clathrate hydrates to deliver the nitrogen component to Jupiter, predicts O/H?9×solar (Gautier et al., 2001, Astrophys. J. 550 (2), L227-L230). Finally we show that the measured condensible volatile vertical profiles in the PES are consistent with column-stretching or entraining downdraft scenarios only if the basic state (the pre-stretched column or the entrainment source region) is described by condensible volatile vertical profiles that are drier than those in the equilibrium cloud condensation models. This dryness is supported by numerous remote sensing results but seems to disagree with observations of widespread clouds on Jupiter at pressure levels predicted by equilibrium cloud condensation models for ammonia and H₂S.     

Laboratory measurements of the microwave opacity of hydrochloric acid vapor in a carbon dioxide atmosphere

Laboratory measurements of the microwave opacity of HCl in a CO₂ atmosphere have been conducted in the S (13.3 cm), X (3.6 cm), and K (1.4 cm) microwave bands at a pressure of 7.2 bar and at two different mixing ratios. The results are consistent with an opacity model employing the Van Vleck-Weisskopf lineshape applied to the published submillimeter line intensities of HCl (JPL Catalog [Pickett et al., 1998, J. Quant. Spectrosc. Rad. Trans. 60, 883-890]) and empirically fitted with a modeled parameter for CO₂ broadening. Based on the deep atmospheric abundance of HCl inferred from near-infrared measurements [Dalton et al., 2000, Bull. Am. Astron. Soc. 32, 1120], the resulting modeled HCl opacity is constrained to have a small effect on the overall microwave absorption spectrum of Venus, but can be used in developing a more accurate radiative transfer model.     

Deuterium chemistry and airglow in the jovian thermosphere

We present a detailed study of the distribution of key deuterated species (viz., atomic D and HD) and the associated deuterium Lyman-α airglow in the jovian thermosphere. The reactions that appear to govern the abundances of these deuterated species are used in conjunction with C₂-chemistry in a 1-D photochemical-diffusion model. While the D abundance is mainly sensitive to H densities and the vibrational temperature profile, the D vertical distribution also depends on other parameters such as eddy mixing and the uncertain values of some of the reaction rate constants. We consider different scenarios by varying several parameters controlling the D distribution in the thermosphere. A radiative transfer model with coupling of the H and D Lyman-α lines is employed to obtain line profiles and total intensities at disk center for these scenarios. This allows a comparison of the impact of various parameters on the jovian D Lyman-α emission. A consequence of these chemical processes in the jovian thermosphere is the formation of CH₂D, CH₃D, and C₂H₅D, and other deuterated species. We also discuss the source of these deuterated hydrocarbons and their abundance. We find that HD vibrational chemistry impacts D in the thermosphere, CH₃D and C₂H₅D are vibrationally enhanced in the thermosphere, and variations in abundance of CH₃D and C₂H₅D in the thermosphere may reflect dynamical activity (i.e., Kh) in the jovian upper atmosphere. An observing program dedicated to providing such measurements of these testable phenomena would provide further insight into the synergistic coupling between chemistry, energetics and airglow in the jovian upper atmosphere.     

Methane absorption in the atmosphere of Jupiter from 1800 to 9500 cm and implications for vertical cloud structure

New measurements of the low-temperature near-infrared absorption of methane (Sihra, 1998, Laboratory measurements of near-infrared methane bands for remote sensing of the jovian atmosphere, Ph.D. thesis, University of Oxford) have been combined with existing, longer path-length, higher-temperature data of Strong et al. (1993, Spectral parameters of self- and hydrogen-broadened methane from 2000 to 9500 cm⁻¹ for remote sounding of the atmosphere of Jupiter, J. Quant. Spectrosc. Radiat. Trans. 50, 309-325) and fitted with band models. The combined data set is found to be more consistent with previous low-temperature methane absorption measurements than that of Strong et al. (1993, J. Quant. Spectrosc. Radiat. Trans. 50, 309-325) but covers the same wider wavelength range and accounts for both self- and hydrogen-broadening conditions. These data have been fitted with k-coefficients in the manner described by Irwin et al. (1996, Calculated k-distribution coefficients for hydrogen- and self-broadened methane in the range 2000-9500 cm⁻¹ from exponential sum fitting to band modelled spectra, J. Geophys. Res. 101, 26,137-26,154) and have been used in multiple-scattering radiative transfer models to assess their impact on our previous estimates of the jovian cloud structure obtained from Galileo Near-Infrared Mapping Spectrometer (NIMS) observations (Irwin et al., 1998, Cloud structure and atmospheric composition of Jupiter retrieved from Galileo NIMS real-time spectra, J. Geophys. Res. 103, 23,001-23,021; Irwin et al., 2001, The origin of belt/zone contrasts in the atmosphere of Jupiter and their correlation with 5-μm opacity, Icarus 149, 397-415; Irwin and Dyudina, 2002, The retrieval of cloud structure maps in the equatorial region of Jupiter using a principal component analysis of Galileo/NIMS data, Icarus 156, 52-63). Although significant differences in methane opacity are found at cooler temperatures, the difference in the optical depth of the atmosphere due to methane is found to diminish rapidly with increasing pressure and temperature and thus has negligible effect on the cloud structure inferred at deeper levels. Hence the main cloud opacity variation is still found to peak at around 1-2 bar using our previous analytical approach, and is thus still in disagreement with Galileo Solid State Imager (SSI) determinations (Banfield et al., 1998, Jupiter's cloud structure from Galileo imaging data, Icarus 135, 230-250; Simon-Miller et al., 2001, Color and the vertical structure in Jupiter's belts, zones and weather systems, Icarus 154, 459-474) which place the main cloud deck near 0.9 bar. Further analysis of our retrievals reveals that this discrepancy is probably due to the different assumptions of the two analyses. Our retrievals use a smooth vertically extended cloud profile while the SSI determinations assume a thin NH₃ cloud below an extended haze. When the main opacity in our model is similarly assumed to be due to a thin cloud below an extended haze, we find the main level of cloud opacity variation to be near the 1 bar level—close to that determined by SSI and moderately close to the expected condensation level of ammonia ice of 0.85 bar, assuming that the abundance of ammonia on Jupiter is (7±1)×¹⁰⁻⁴ (Folkner et al., 1998, Ammonia abundance in Jupiter's atmosphere derived from the attenuation of the Galileo probe's radio signal, J. Geophys. Res. 103, 22,847-22,855; Atreya et al., 1999, A comparison of the atmospheres of Jupiter and Saturn: deep atmospheric composition, cloud structure, vertical mixing, and origin, Planet. Space Sci. 47, 1243-1262). However our data in the 1-2.5 μm range have good height discrimination and our lowest estimate of the cloud base pressure of 1 bar is still too great to be consistent with the most recent estimates of the ammonia abundance of 3.5 × solar. Furthermore the observed limited spatial distribution of ammonia ice absorption features on Jupiter suggests that pure ammonia ice is only present in regions of localised vigorous uplift (Baines et al., 2002, Fresh ammonia ice clouds in Jupiter: spectroscopic identification, spatial distribution, and dynamical implications, Icarus 159, 74-94) and is subsequently rapidly modified in some way which masks its pure absorption features. Hence we conclude that the main cloud deck on Jupiter is unlikely to be composed of pure ammonia ice and instead find that it must be composed of either NH₄SH or some other unknown combination of ammonia, water, and hydrogen sulphide and exists at pressures of between 1 and 2 bar.     

Search for spatial variation in the jovian N/N ratio from Cassini/CIRS observations

We have used the spectra obtained by the Composite Infrared Spectrometer (CIRS) onboard the Cassini spacecraft to search for latitudinal variation in the ¹⁵N/¹⁴N ratio on Jupiter. We found no variations statistically significant given the observational and model uncertainties. The absence of latitudinal variations demonstrates that ¹⁵NH₃ is not fractionated in Jupiter's atmosphere, and that the measured ¹⁵N/¹⁴N represents Jupiter's global value. Our mean value for the global jovian ¹⁵N/¹⁴N ratio of (2.22±0.52)×10⁻³ agrees with previous measurements made by Fouchet et al. (2000, Icarus 143, 223-243) and Owen et al. (2001, Astrophys. J. 553, L77-L79). We argue that the jovian isotopic ¹⁵N/¹⁴N ratio must represent the solar nitrogen isotopic composition. The solar ¹⁵N/¹⁴N ratio hence significantly differs from the terrestrial value: (¹⁵N/¹⁴N)_⊕=3.68×10⁻³. This supports the proposition that terrestrial nitrogen originates from a nitrogen reservoir isolated from the main nitrogen reservoir in the proto-solar nebula. The origin and carrier of this isolated reservoir are still unknown.     

Laboratory measurements of the microwave opacity of gaseous Ammonia (NH3) under simulated conditions for the Jovian atmosphere

Gaseous ammonia (NH₃) has long been recognized as a primary source of microwave opacity in the atmosphere of Jupiter. In order to more accurately infer the abundance and distribution of ammonia from radio emission measurements in the 1 to 20-cm wavelength range and radio occultation measurements at 3.6 and 13 cm, we have made measurements of the microwave opacity from gaseous ammonia under simulated conditions for the Jovian atmosphere. Measurements of ammonia absorptivity were made at five frequencies from 1.62 to 21.7 GHz (wavelengths from 18.5 to 1.38 cm), at temperatures from 178 to 300°K, and at pressures from 1 to 6 atm, in a 90% hydrogen/10% helium atmosphere. The results of these measurements show that in the 1.38- to 18.5-cm wavelength range, the absorption from gaseous ammonia is correctly expressed by the modified Ben-Reuven lineshape as per G.L. Berge and S. Gulkis (1976, Earth-based radio observations of Jupiter: Millimeter to meter wavelengths. In Jupiter (T. Gehrels, Ed.), pp. 621–692, Univ. of Arizona Press, Tucson). When applied to the microwave opacity measured by radio occultation measurements, or the microwave opacity inferred from radio emmission measurements, these results suggest that either an abundance of ammonia 1.5 to 2.0 times greater than the solar abundance must exist at levels below the 1- to 2-bar pressure range, or that some other microwave absorber must be present.We conclude by suggesting further laboratory measurements of other potential microwave-absorbing constituents and additional investigation of the microwave absorption from ammonia in the 10- to 20-cm wavelength range and at wavelengths shortward of 1 cm.     

Saturn's latitudinal C2H2 and C2H6 abundance profiles from Cassini/CIRS and ground-based observations

Hydrocarbons in the upper atmosphere of Saturn are known, from Voyager, ground-based, and early Cassini results, to vary in emission intensity with latitude. Of particular interest is the marked increase in hydrocarbon line intensity near the south pole during southern summer, as the increased line intensity cannot be simply explained by the increased temperatures observed in that region since the variations between C₂H₂ and C₂H₆ emission in the south pole region are different. In order to measure the latitudinal variations of hydrocarbons in Saturn's southern hemisphere we have used 3 cm⁻¹ resolution Cassini CIRS data from 2006 and combined this with measurements from the ground in October 2006 at NASA's IRTF using Celeste, an infrared high-resolution cryogenic grating spectrometer. These two data sets have been used to infer the molecular abundances of C₂H₂ and C₂H₆ across the southern hemisphere in the 1-10 mbar altitude region. We find that the latitudinal acetylene profile follows the yearly average mean daily insolation except at the southern pole where it peaks in abundance. Near the equator (5° S) the C₂H₂ abundance at the 1.2 mbar level is (1.6±0.19)×¹⁰−7 and it decreases by a factor of 2.7 from the equator toward the pole. However, at the pole (∼87° S) the C₂H₂ abundance jumps to (1.8±0.3)×¹⁰−7, approximately the equatorial value. The C₂H₆ abundance near the equator at the 2 mbar level is (0.7±0.1)×¹⁰−5 and stays approximately constant until mid-latitudes where it increases gradually toward the pole, attaining a value of (1.4±0.4)×¹⁰−5 there. The increase in ethane toward the pole with the corresponding decrease in acetylene is consistent with southern hemisphere meridional winds [Greathouse, T.K., Lacy, J.H., Bézard, B., Moses, J.I., Griffith, C.A., Richter, M.J., 2005. Icarus 177, 18-31]. The localized increase in acetylene at the pole provides evidence that there is dynamical transport of hydrocarbons from the equator to the southern pole.     

Broadband Submillimeter Spectroscopy of HCN, NH3, and PH3in the Troposphere of Jupiter

We report measurements of the Jupiter brightness spectrum in the 850-μm and 1100-μm atmospheric windows with a spectral resolution of 125 MHz, obtained with a Fourier transform spectrometer on the James Clerk Maxwell Telescope. Three results were obtained. First, the predicted absorption features due to the rotational lines of HCN at 266 and 354 GHz were not detected within our error limits of less than 1%. We establish new upper limits for the HCN abundance in the jovian troposphere for five assumed abundance distributions and for two assumed NH₃abundances. The upper limits are 1.7 to 13 times smaller than the abundance value obtained in the only reported detection of HCN in Jupiter prior to the impact of Shoemaker–Levy 9. Second, the continuum brightness temperature spectrum at 850 μm was determined and is in agreement with previous measurements, but has large error bars due to uncertainties in the photometric calibration. We estimate the ammonia abundance in the 1–2 bar region to be 1.7 times solar, but this result is tentative since scattering by NH₃cloud particles and absorption by gaseous H₂S were neglected in our atmospheric model. Finally, the first rotational line of PH₃at 267 GHz was not detected, a result which we demonstrate is consistent with the statistical noise level in these measurements, with current values of the spectroscopic parameters, and with phosphine measurements at other wavelengths.     

Surface-bounded atmosphere of Europa

A 1-D collisional Monte Carlo model of Europa's atmosphere is described in which the sublimation and sputtering sources of H₂O molecules and their molecular fragments are accounted for as well as the radiolytically produced O₂. Dissociation and ionization of H₂O and O₂ by magnetospheric electron, solar UV-photon and photo-electron impact, and collisional ejection from the atmosphere by the low-energy plasma are taken into account. Reactions with the surface are discussed, but only adsorption and atomic oxygen recombination are included in this model. The size of the surface-bounded oxygen atmosphere of Europa is primarily determined by a balance between atmospheric sources from irradiation of the satellite's icy surface by the high-energy magnetospheric charged particles and atmospheric losses from collisional ejection by the low-energy plasma, photo- and electron-impact dissociation, and ionization and pick-up from the surface-bounded atmosphere. A range of sources rates for O₂ to H₂O are used with a larger oxygen-to-water ratio than suggested by laboratory measurements in order to account for differences in adsorption onto grains in the regolith. These calculations show that the atmospheric composition is determined by both the water and oxygen photochemistry in the near-surface region, escape of suprathermal oxygen and water into the jovian system, and the exchange of radiolytic water products with the porous regolith. For the electron impact ionization rates used, pick-up ionization is the dominant oxygen loss process, whereas photo-dissociation and atmospheric sputtering are the dominant sources of neutral oxygen for Europa's neutral torus. Including desorption and loss of water enhances the supply of oxygen species to the neutral torus, but hydrogen produced by radiolysis is the dominant source of neutrals for Europa's torus in these models.     

Water vapor variations in the Venus mesosphere from microwave spectra

Mm-wave spectra of HDO in the Venus mesosphere (65-100 km) were obtained over the period March 1998 to June 2004. Each spectrum is a measurement of the hemispheric-average H₂O vapor mixing ratio in the Venus mesosphere. Observations were conducted for wide ranges of Venus solar elongations (46° W to 47° E), and fractional disk illuminations (f=0% to 99%), yielding water vapor abundances on 17 dates and over a full range of local solar time (LST) at the sub-Earth point on Venus. Our mesopheric H₂O values are more numerous and far more precise than the earliest mm-derived H₂O measurements [Encrenaz, Th., Lellouch, E., Paubert, G., Gulkis, S., 1991. First detection of HDO in the atmosphere of Venus at radio wavelengths: An estimate of the H₂O vertical distribution. Astron. Astrophys. 246, L63-L66; Encrenaz, Th., Lellouch, E., Cernicharo, J., Paubert, G., Gulkis, S., Spilker, T., 1995. The thermal profile and water abundance in the Venus mesosphere from H₂O and HDO millimeter observations. Icarus 117, 162-172], allowing an analysis of variability that was previously impossible. Measured 65-100 km H₂O ranged from 0.0±0.06 to 3.5±0.3 ppmv, with significantly different variability than found in previous infrared (lower altitude, cloudtop) studies. Strong global variability on a 1-2 month timescale is clear and unambiguous. A limited number of excellent s/n measurements tentatively indicate the 1-2 month variability manifests most rapidly as change in the lower mesosphere, and more slowly as change in the upper mesosphere. Neither long term (1998-2004) nor diurnal variability in 65-100 km H₂O is evident. While six-year and/or diurnal variabilities are not ruled out, they are weaker than the 1-2 month timescale variation. These conclusions are supported by initial (2004) sub-mm measurements.     

Molecular hydrogen in Titan’s atmosphere: Implications of the measured tropospheric and thermospheric mole fractions

The third most abundant species in Titan’s atmosphere is molecular hydrogen with a tropospheric/lower stratospheric mole fraction of 0.001 derived from Voyager and Cassini infrared measurements. The globally averaged thermospheric H₂ mole fraction profile from the Cassini Ion Neutral Mass Spectrometer (INMS) measurements implies a small positive gradient in the H₂ mixing ratio from the tropopause region to the lower thermosphere (∼950-1000 km), which drives a downward H₂ flux into Titan’s surface comparable to the H₂ escape flux out of the atmosphere (∼2 × 10¹⁰ cm⁻² s⁻¹ referenced to the surface) and requires larger photochemical production rates of H₂ than obtained by previous photochemical models. From detailed model calculations based on known photochemistry with eddy, molecular, and thermal diffusion, the tropospheric and thermospheric H₂ mole fractions are incompatible by a factor of ∼2. The measurements imply that the downward H₂ surface flux is in substantial excess of the speculative threshold value for methanogenic life consumption of H₂ (McKay, C.P., Smith, H.D. [2005], Icarus 178, 274-276. doi:10.1016/j.icarus.2005.05.018), but without the extreme reduction in the surface H₂ mixing ratio.     

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.     

Reconciling the centimeter- and millimeter-wavelength ammonia absorption spectra under jovian conditions: Extensive millimeter-wavelength measurements and a consistent model

Over 1000 laboratory measurements of the 2-4 mm-wavelength opacity of ammonia have been made under simulated jovian atmospheric conditions using a high-precision laboratory system developed at Georgia Tech. These laboratory measurements of the opacity of ammonia were made of various gas mixtures of hydrogen (∼77.5-85.5%), helium (∼12.5-13.5%), and ammonia (1-10%) at pressures between 1 and 3 bars and temperatures between 200 and 300 K. Laboratory measurements were also made of the opacity of pure ammonia at pressures between 0.05 and 1 bar and temperatures between 200 and 300 K. Using these millimeter-wavelength measurements and close to 2000 cm-wavelength measurements made by Hanley et al. (2009), a new consistent model has been developed to accurately characterize the absorption spectra of ammonia in a hydrogen/helium atmosphere in the 1 mm to 30 cm wavelength range. This model can be used in the 1-30 cm wavelength range at pressures up to 20 bars and temperatures from 200 to 500 K and in the 1 mm to 1 cm wavelength range at pressures up to 3 bars and temperatures from 200 to 300 K. These measurements and the accompanying model will enable better interpretation of the centimeter- and millimeter-wavelength emission spectra of the jovian planets.     

The mean Jovian temperature structure derived from spectral observations from 105 to 630 cm−1

New far-infrared observations of the NH₃ rotation-inversion manifolds in the spectrum of Jupiter have been inverted with the use oftthe detailed ammonia line opacity. A temperature of 160°K at a 1-bar pressure level and a temperature of 105°K for the minimum temperature of the inversion level at 0.15 bars have been derived for gaseous absorption due to NH₃, H₂, and He. The overall fit to the brightness temperature as a function of frequency σ is within ±1°K for 100 ≤ σ ≤ 400 cm^?1 except for the centers of the NH₃ rotation-inversion manifolds where for J ≥ 7 the fit is about 5°K too high. In the continuum for 400 ≤ σ ≤ 630 cm^?1 the fit is within 2.5°K. Consideration of an ammonia ice haze, photodissociation of NH₃ by uv radiation, NH₃ abundance variation, different He/H₂ ratios, and uncertainties in the data effect the temperatures at 1 bar and the temperature at the inversion layer by <7°K. The presently derived temperature at 1 bar of 160°K is consistent with Jovian interior models which can match the gravitational moment, J₂.     

Observations with the Visual and Infrared Mapping Spectrometer (VIMS) during Cassini's flyby of Jupiter

The Cassini Visual and Infrared Mapping Spectrometer (VIMS) is an imaging spectrometer covering the wavelength range 0.3-5.2 μm in 352 spectral channels, with a nominal instantaneous field of view of 0.5 mrad. The Cassini flyby of Jupiter represented a unique opportunity to accomplish two important goals: scientific observations of the jovian system and functional tests of the VIMS instrument under conditions similar to those expected to obtain during Cassini's 4-year tour of the saturnian system. Results acquired over a complete range of visual to near-infrared wavelengths from 0.3 to 5.2 μm are presented. First detections include methane fluorescence on Jupiter, a surprisingly high opposition surge on Europa, the first visual-near-IR spectra of Himalia and Jupiter's optically-thin ring system, and the first near-infrared observations of the rings over an extensive range of phase angles (0-120°). Similarities in the center-to-limb profiles of H⁺₃ and CH₄ emissions indicate that the H⁺₃ ionospheric density is solar-controlled outside of the auroral regions. The existence of jovian NH₃ absorption at 0.93 μm is confirmed. Himalia has a slightly reddish spectrum, an apparent absorption near 3 μm, and a geometric albedo of 0.06±0.01 at 2.2 μm (assuming an 85-km radius). If the 3-μm feature in Himalia's spectrum is eventually confirmed, it would be suggestive of the presence of water in some form, either free, bound, or incorporated in layer-lattice silicates. Finally, a mean ring-particle radius of 10 μm is found to be consistent with Mie-scattering models fit to VIMS near-infrared observations acquired over 0-120° phase angle.     

High-resolution spectroscopy of Saturn at 3 microns: CH4, CH3D, C2H2, C2H6, PH3, clouds, and haze

We report observation and analysis of a high-resolution 2.87-3.54 μm spectrum of the southern temperate region of Saturn obtained with NIRSPEC at Keck II. The spectrum reveals absorption and emission lines of five molecular species as well as spectral features of haze particles. The ν₂+ν₃ band of CH₃D is detected in absorption between 2.87 and 2.92 μm; and we derived from it a mixing ratio approximately consistent with the Infrared Space Observatory result. The ν₃ band of C₂H₂ also is detected in absorption between 2.95 and 3.05 μm; analysis indicates a sudden drop in the C₂H₂ mixing ratio at 15 mbar (130 km above the 1 bar level), probably due to condensation in the low stratosphere. The presence of the ν₃+ν₉+ν₁₁ band of C₂H₆ near 3.07 μm, first reported by Bjoraker et al. [Bjoraker, G.L., Larson, H.P., Fink, U., 1981. Astrophys. J. 248, 856-862], is confirmed, and a C₂H₆ condensation altitude of 10 mbar (140 km) in the low stratosphere is determined. We assign weak emission lines within the 3.3 μm band of CH₄ to the ν₇ band of C₂H₆, and derive a mixing ratio of 9±4×¹⁰⁻⁶ for this species. Most of the C₂H₆ 3.3 μm line emission arises in the altitude range 460-620 km (at ∼μbar pressure levels), much higher than the 160-370 km range where the 12 μm thermal molecular line emission of this species arises. At 2.87-2.90 μm the major absorber is tropospheric PH₃. The cloud level determined here and at 3.22-3.54 is 390-460 mbar (∼30 km), somewhat higher than found by Kim and Geballe [Kim, S.J., Geballe, T.R., 2005. Icarus 179, 449-458] from analysis of a low resolution spectrum. A broad absorption feature at 2.96 μm, which might be due to NH₃ ice particles in saturnian clouds, is also present. The effect of a haze layer at about 125 km (∼12 mbar level) on the 3.20-3.54 μm spectrum, which was not apparent in the low resolution spectrum, is clearly evident in the high resolution data, and the spectral properties of the haze particles suggest that they are composed of hydrocarbons.     

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).