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1.
We present near-IR spectra of solid CO2 in H2O and CH3OH, and find they are significantly different from that of pure solid CO2. Peaks not present in either pure H2O or pure CO2 spectra become evident when the two are mixed. First, the putative theoretically forbidden CO2 (2ν3) overtone near 2.134 μm (4685 cm−1), that is absent from our spectrum of pure solid CO2, is prominent in the spectra of H2O/CO2=5 and 25 mixtures. Second, a 2.74-μm (3650 cm−1) dangling OH feature of H2O (and a potentially related peak at 1.89 μm) appear in the spectra of CO2-H2O ice mixtures, but are probably not diagnostic of the presence of CO2. Other CO2 peaks display shifts in position and increased width because of intermolecular interactions with H2O. Warming causes some peak positions and profiles in the spectrum of a H2O/CO2=5 mixture to take on the appearance of pure CO2. Absolute strengths for absorptions of CO2 in solid H2O are estimated. Similar results are observed for CO2 in solid CH3OH. Since the CO2 (2ν3) overtone near 2.134 μm (4685 cm−1) is not present in pure CO2 but prominent in mixtures, it may be a good observational (spectral) indicator of whether solid CO2 is a pure material or intimately mixed with other molecules. These observations may be applicable to Mars polar caps as well as outer Solar System bodies.  相似文献   

2.
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.  相似文献   

3.
Hydrocarbons such as acetylene (C2H2) and ethane (C2H6) are important tracers in Jupiter's atmosphere, constraining our models of the chemical and dynamical processes. However, our knowledge of the vertical and meridional variations of their abundances has remained sparse. During the flyby of the Cassini spacecraft in December 2000, the Composite Infrared Spectrometer (CIRS) instrument was used to map the spatial variation of emissions from 10 to 1400 cm−1 (1000-7 μm). In this paper we analyze a zonally averaged set of CIRS spectra taken at the highest (0.48 cm−1) resolution, firstly to infer atmospheric temperatures in the stratosphere at 0.5-20 mbar via the ν4 band of CH4, and in the troposphere at 150-400 mbar, via the H2 absorption at 600-800 cm−1. Stratospheric temperatures at 5 mbar are generally warmer in the north than the south by 7-8 K, while tropospheric temperatures show no such asymmetry. Both latitudinal temperature profiles however do show a pattern of maxima and minima which are largely anti-correlated between the two levels. We then use the derived temperature profiles to infer the vertical abundances of C2H2 and C2H6 by modeling tropospheric absorption (∼200 mbar) and stratospheric emission (∼5 mbar) in the C2H2ν5 and C2H6ν9 bands, and also emission of the acetylene (ν4+ν5)−ν4 hotband (∼0.1 mbar). Acetylene shows a distinct north-south asymmetry in the stratosphere, with 5 mbar abundances greatest close to 20° N and decreasing from there towards both poles by a factor of ∼4. At 200 mbar in contrast, acetylene is nearly flat at a level of ∼3×10−9. Additionally, the abundance gradient of C2H2 between 10 and 0.1 mbar is derived, based on interpolated temperatures at 0.1 mbar, and is found to be positive and uniform with latitude to within errors. Ethane at both 5 and 200 mbar shows increasing VMR towards polar regions of ∼1.75 towards 70° N and ∼2.0 towards 70° S. An explanation for the meridional trends is proposed in terms of a combination of photochemistry and dynamics. Poleward, the decreasing UV flux is predicted to decrease the abundances of C2H2 and C2H6 by factors of 2.7 and 3.5, respectively, at latitude 70°. However, the lifetime of C2H6 in the stratosphere (3×1010 s at 5 mbar) is much longer than the dynamical timescale for meridional mixing inferred from Comet SL-9 debris (5-50×108 s), and therefore the rising abundance towards high latitudes likely indicates that meridional mixing dominates over photochemical effects. For C2H2, the opposite occurs, with the relatively short photochemical lifetime (3×107 s), compared to meridional mixing times, ensuring that the expected photochemical trends are visible.  相似文献   

4.
Sang J. Kim  T.R. Geballe 《Icarus》2005,179(2):449-458
We have used synthetic spectra to analyze a medium resolution 2.9-4.2 μm spectrum of Saturn's temperate region observed at UKIRT using CGS4. The synthetic spectra include CH4, PH3, and NH3 lines, for which mixing ratios were adopted from recent Cassini results. The observed absorption features in the spectrum are well accounted for by lines of these molecular species formed 22 +/− 8 km above the 1 bar pressure level at ∼610 mbar. The influence of optically thin haze particles at higher altitudes on the spectrum is not pronounced, with higher spectral resolution probably required to constrain the effects of haze in this wavelength region. Fluorescent line emission by CH4 in its ν3 and ν3+ν4−ν4 bands, detected in the 3.2-3.5 μm region, originates between 400 km (∼0.06 mbar) and 800 km (∼0.01 μbar) above the 1 bar level, with peak contributions from the two major contributing bands at 550 km (∼3 μbar) and 700 km (∼0.1 μbar), respectively.  相似文献   

5.
We present spectra of Saturn's icy satellites Mimas, Enceladus, Tethys, Dione, Rhea, and Hyperion, 1.0-2.5 μm, with data extending to shorter (Mimas and Enceladus) and longer (Rhea and Dione) wavelengths for certain objects. The spectral resolution (R=λ/Δλ) of the data shown here is in the range 800-1000, depending on the specific instrument and configuration used; this is higher than the resolution (R=225 at 3 μm) afforded by the Visual-Infrared Mapping Spectrometer on the Cassini spacecraft. All of the spectra are dominated by water ice absorption bands and no other features are clearly identified. Spectra of all of these satellites show the characteristic signature of hexagonal H2O ice at 1.65 μm. We model the leading hemisphere of Rhea in the wavelength range 0.3-3.6 μm with the Hapke and the Shkuratov radiative transfer codes and discuss the relative merits of the two approaches to fitting the spectrum. In calculations with both codes, the only components used are H2O ice, which is the dominant constituent, and a small amount of tholin (Ice Tholin II). Tholin in small quantities (few percent, depending on the mixing mechanism) appears to be an essential component to give the basic red color of the satellite in the region 0.3-1.0 μm. The quantity and mode of mixing of tholin that can produce the intense coloration of Rhea and other icy satellites has bearing on its likely presence in many other icy bodies of the outer Solar System, both of high and low geometric albedos. Using the modeling codes, we also establish detection limits for the ices of CO2 (a few weight percent, depending on particle size and mixing), CH4 (same), and NH4OH (0.5 weight percent) in our globally averaged spectra of Rhea's leading hemisphere. New laboratory spectral data for NH4OH are presented for the purpose of detection on icy bodies. These limits for CO2, CH4, and NH4OH on Rhea are also applicable to the other icy satellites for which spectra are presented here. The reflectance spectrum of Hyperion shows evidence for a broad, unidentified absorption band centered at 1.75 μm.  相似文献   

6.
We present 0.8-2.4 μm spectral observations of uranian satellites, obtained at IRTF/SpeX on 17 nights during 2001-2005. The spectra reveal for the first time the presence of CO2 ice on the surfaces of Umbriel and Titania, by means of 3 narrow absorption bands near 2 μm. Several additional, weaker CO2 ice absorptions have also been detected. No CO2 absorption is seen in Oberon spectra, and the strengths of the CO2 ice bands decline with planetocentric distance from Ariel through Titania. We use the CO2 absorptions to map the longitudinal distribution of CO2 ice on Ariel, Umbriel, and Titania, showing that it is most abundant on their trailing hemispheres. We also examine H2O ice absorptions in the spectra, finding deeper H2O bands on the leading hemispheres of Ariel, Umbriel, and Titania, but the opposite pattern on Oberon. Potential mechanisms to produce the observed longitudinal and planetocentric distributions of the two ices are considered.  相似文献   

7.
We present a preliminary analysis of CH4 absorptions near 6800 Å in new high resolution spectra of Uranus. A curve of growth analysis of the data yields a rotational temperature near 100 K and a CH4/H2 ratio that is 1 to 3 times that expected for a solar type composition. The long pathlengths of CH4, apparently demanded by absorptions near 4700 Å, are qualitatively shown to be the result of line formation in a deep, predominantly Rayleigh scattering atmosphere in which continuum absorption is a strong function of wavelength. The analysis of the CH4 also yields a minimum value for the effective pressure of line formation (～ 2 atm). This value is shown to be twice that expected on Uranus if the atmosphere were predominantly H2. It is speculated that large amounts of some otherwise optically inert gas is present in the Uranus atmosphere. N2 is suggested as a possible candidate since there are cosmogonic reasons why Uranus should contain large amounts of N relative to C, He, and H, and also because the pressure-induced pure rotation spectrum of N2 could possibly account for the low brightness temperatures that have recently been observed at 33 and 350 μm. If N2 is present the planet probably possesses a surface at the 10–100 atmosphere level.  相似文献   

8.
A spectrum of Jupiter between 6000 and 12 000 cm? at high resolution (0.05 cm?) was recorded with a Michelson interferometer at Palomar Mountain in October 1974. An analysis of the R branch of the 3ν3CH4 band with the reflecting-layer model, taking into account the H2 absorption which occurs in the same spectral range, leads to a Lorentzian half-width of 0.09 ± 0.02 cm?1, a rotational temperature of 175 ± 10° K, and a CH4 abundance of order 52m atm. Five lines of the 13CH43ν3 band have been identified; a comparison with new laboratory spectra indicates that the 13CH4/12CH4 ratio in the Jupiter atmosphere is close to the terrestrial ratio.  相似文献   

9.
The nucleus of Comet C/2001 A2 (LINEAR) split several times during its recent apparition, presenting an unusual opportunity to search for chemical differences in freshly exposed material. We conducted this search using NIRSPEC at the W.M. Keck Observatory on four dates in 2001: 9.5 and 10.5 July and 4.4 and 10.5 August. We detected the R0 and R1 lines of the ν3 vibrational band of CH4 near 3.3 μm on all dates. The R2 line was detected on 4.4 and 10.5 August. When we compare production rates of CH4 to H2O, we find evidence of a significant enhancement in August relative to that found in July. H2CO was securely detected via its ν1 and ν5 bands on 9.5 July. On 10.5 July, H2CO emission was much weaker, and its mixing ratio had dropped by a factor of about four. The mixing ratios for other detected volatile species did not change significantly over the course of the observations. We discuss the implications of this evidence for chemical heterogeneity in the nucleus of Comet C/2001 A2.  相似文献   

10.
We report the detection of 13CH3D in Titan's stratosphere from Cassini/CIRS infrared spectra near 8.7 μm. Fitting simultaneously the ν6 bands of both 13CH3D and 12CH3D and the ν4 band of CH4, we derive a D/H ratio equal to and a 12C/13C ratio in deuterated methane of , consistent with that measured in normal methane.  相似文献   

11.
New thermal profiles of Jupiter are retrieved from recent far infrared spectral measurements and for H2 mixing ratios varying from 0.8 to 0.94. The effective temperature corresponding to the inferred thermal profile is 123.15 ± 0.35°K. Far-infrared brightness temperature spectra computed from these profiles are compared to experimental data including measurements made at high spectral resolution in the NH3ν2 band at 10 μm and in NH3 pure rotational bands between 40 and 110 μm. It is found that a strong depletion of NH3 does occur in the Jovian stratosphere and that ammonia seems to be undersaturated in the upper troposphere.  相似文献   

12.
T.Y Brooke  H.A Weaver  G Chin  S.J Kim 《Icarus》2003,166(1):167-187
High resolution infrared spectra of Comet C/1995 O1 (Hale-Bopp) were obtained during 2-5 March 1997 UT from the NASA Infrared Telescope Facility on Mauna Kea, Hawaii, when the comet was at r≈1.0 AU from the Sun pre-perihelion. Emission lines of CH4, C2H6, HCN, C2H2, CH3OH, H2O, CO, and OH were detected. The rotational temperature of CH4 in the inner coma was Trot=110±20 K. Spatial profiles of CH4, C2H6, and H2O were consistent with release solely from the nucleus. The centroid of the CO emission was offset from that of the dust continuum and H2O. Spatial profiles of the CO lines were much broader than those of the other molecules and asymmetric. We estimate the CO production rate using a simplified outflow model: constant, symmetric outflow from the peak position. A model of the excitation of CO that includes optical depth effects using an escape probability method is presented. Optical depth effects are not sufficient to explain the broad spatial extent. Using a parent+extended-source model, the broad extent of the CO lines can be explained by CO being produced mostly (∼90% on 5 March) from an extended source in the coma. The CO rotational temperature was near 100 K. Abundances relative to H2O (in percent) were 1.1±0.3 (CH4), 0.39±0.10 (C2H6), 0.18±0.04 (HCN), 0.17±0.04 (C2H2), 1.7±0.5 (CH3OH), and 37-41 (CO, parent+extended source). These are roughly comparable to those obtained for other long-period comets also observed in the infrared, though CO appears to vary.  相似文献   

13.
The infrared AOTF spectrometer is a part of the SPICAM experiment onboard the Mars-Express ESA mission. The instrument has a capability of solar occultations and operates in the spectral range of 1-1.7 μm with a spectral resolution of ∼3.5 cm−1. We report results from 24 orbits obtained during MY28 at Ls 130°-160°, and the latitude range of 40°-55° N. For these orbits the atmospheric density from 1.43 μm CO2 band, water vapor mixing ratio based on 1.38 μm absorption, and aerosol opacities were retrieved simultaneously. The vertical resolution of measurements is better than 3.5 km. Aerosol vertical extinction profiles were obtained at 10 wavelengths in the altitude range from 10 to 60 km. The interpretation using Mie scattering theory with adopted refraction indices of dust and H2O ice allows to retrieve particle size (reff∼0.5-1 μm) and number density (∼1 cm−3 at 15-30 km) profiles. The haze top is generally below 40 km, except the longitude range of 320°-50° E, where high-altitude clouds at 50-60 km were detected. Optical properties of these clouds are compatible with ice particles (effective radius reff=0.1-0.3 μm, number density N∼10 cm−3) distributed with variance νeff=0.1-0.2 μm. The vertical optical depth of the clouds is below 0.001 at 1 μm. The atmospheric density profiles are retrieved from CO2 band in the altitude range of 10-90 km, and H2O mixing ratio is determined at 15-50 km. Unless a supersaturation of the water vapor occurs in the martian atmosphere, the H2O mixing ratio indicates ∼5 K warmer atmosphere at 25-45 km than predicted by models.  相似文献   

14.
Using synthetic spectra derived from an updated model atmosphere together with a continuum model that includes contributions from haze, cloud and ground, we have re-analyzed the recently published (Geballe et al., 2003, Astrophys. J. 583, L39-L42) high-resolution 3 μm spectrum of Titan which contains newly-detected bands of HCN (in emission) and C2H2 and CH3D (in absorption), in addition to previously detected bands of CH4. In the 3.10-3.54 μm interval the analysis yields strong evidence for the existence of a cloud deck or optically thick haze layer at about the 10 mbar (∼ 100 km) level. The haze must extend well above this altitude in order to mask the strong CH4 lines at 3.20-3.50 μm. These cloud and haze components must be transparent at 2.87-2.92 μm, where analysis of the CH3D spectrum demonstrates that Titan's surface is glimpsed through a second cloud deck at about the 100 mbar (∼ 50 km) level. Through a combination of areal distribution and optical depth this cloud deck has an effective transmittance of ∼ 20%. The spectral shape of Titan's continuum indicates that the higher altitude cloud and haze particles responsible for suppressing the CH4 absorptions have a largely organic make-up. The rotational temperature of the HCN ranges from 140 to 180 K, indicating that the HCN emission occurs over a wide range of altitudes. This emission, remodeled using an improved collisional deactivation rate, implies mesospheric mixing ratio curves that are consistent with previously predictions. The stratospheric and mesospheric C2H2 mixing ratios are ∼10−5, considerably less than previous model predictions (Yung et al., 1984), but approximately consistent with recent observational results. Upper limits to mixing ratios of HC3N and C4H2 are derived from non-detections of those species near 3.0 μm.  相似文献   

15.
L.M. Trafton 《Icarus》1975,24(4):443-453
Detailed analysis of the R(5) manifold of Titan's 3ν3 CH4 band confirms that the column abundance of Titan's spectroscopically visible atmosphere is greater than 1.6 kmamagats. This agrees with the value estimated from the strength of Titan's 3ν3 CH4Q branch and is at least 25 times the value for the column abundance of Mars' atmosphere. Moreover, the enhanced strength of the weaker CH4 lines in Titan's spectrum relative to Saturn's spectrum suggests that CH4 constitutes a significant fraction of this bulk.Recently discovered strong, unidentified absorptions in Titan's spectrum at 1.05–1.06 μm have been compared with laboratory spectra of a number of gases including CH4, C2H4, C2H6, and C3H8 with negative results. These comparisons, however, have not excluded the possibility that these features arise from a very large quantity of CH4 or from an isotope of CH4. The fundamental transition of the responsible molecule may affect the interpretation of Titan's 8–14 μm spectrum since its wavelength may lie in this window. Comparison with Uranus' spectrum suggests that the visible abundance of this molecule in Titan's atmosphere may be much greater than in Uranus' relatively clear, deep atmosphere.Spectra of features at λ8150.7 and λ8272.7 attributed possibly to H2 have been obtained at high resolution also during the apparitions of 1971, 1972, and 1973. These are presented for comparison with the results of the 1970 apparition. The existence of the λ8150.7 feature is established definitively but further observations are needed to establish whether the λ8272.7 feature exists beyond doubt.  相似文献   

16.
O. Gomis  G. Strazzulla 《Icarus》2005,177(2):570-576
In this work we report on new experiments of ion irradiation of water ice deposited on top of solid carbonaceous materials to study the production of CO2 at the interface ice/refractory material and discuss the possibility that this mechanism accounts for the quantity of CO2 ice detected on the surfaces of the Galilean satellites. The used experimental technique has been in situ infrared spectroscopy. We have irradiated thin films of H2O frost on carbonaceous layers with 200 keV of He+ and Ar+, and 30 keV of He+ at 16 and 80 K. The used carbonaceous layers have been asphaltite, a natural bitumen, and solid organic residues obtained by irradiation of frozen benzene. In both cases the results show that CO2 is produced very efficiently after irradiation obtaining a maximum quantity of the order of . These results are, also quantitatively similar, to those recently obtained for water ice deposited on amorphous carbon films [Mennella, V., Palumbo, M.E., Baratta, G.A., 2004. Formation of CO and CO2 molecules by ion irradiation of water ice covered hydrogenated carbon grains. Astrophys. J. 615, 1073-1080]. Thus we suggest that, whatever is the carbonaceous residue, CO2 will be produced efficiently by the studied process. These results have interest in the context of the surfaces of the icy Galilean satellites in which CO2 has been detected mainly trapped in the non-ice material, not in the pure water ice. We suggest that radiolysis of mixtures of water ice and refractory carbonaceous materials is the primary formation mechanism responsible for the CO2 formation on the surfaces of the Galilean satellites.  相似文献   

17.
E.L. Gibb  M.J. Mumma  M.A. DiSanti 《Icarus》2003,165(2):391-406
We detected CH4 in eight Oort cloud comets using high-dispersion (λ/Δλ∼2×104) infrared spectra acquired with CSHELL at NASA's IRTF and NIRSPEC at the W.M. Keck Observatory. The observed comets were C/1995 O1 (Hale-Bopp), C/1996 B2 (Hyakutake), C/1999 H1 (Lee), C/1999 T1 (McNaught-Hartley), C/1999 S4 (LINEAR), C/2000 WM1 (LINEAR), C/2001 A2 (LINEAR), and 153/P Ikeya-Zhang (C/2002 C1). We detected the R0 and R1 lines of the ν3 vibrational band of CH4 near 3.3 μm in each comet, with the exception of McNaught-Hartley where only the R0 line was measured. In order to obtain production rates, a fluorescence model has been developed for this band of CH4. We report g-factors for the R0 and R1 transitions at several rotational temperatures typically found in comet comae and relevant to our observations. Using g-factors appropriate to Trot as determined from HCN, CO and/or H2O and C2H6, CH4 production rates and mixing ratios are presented. Abundances of CH4/H2O are compared among our existing sample of comets, in the context of establishing their place of origin. In addition, CH4 is compared to native CO, another hypervolatile species, and no correlation is found among the comets observed.  相似文献   

18.
Jeremy Bailey  Linda Ahlsved 《Icarus》2011,213(1):218-232
We have obtained spatially resolved spectra of Titan in the near-infrared J, H and K bands at a resolving power of ∼5000 using the near-infrared integral field spectrometer (NIFS) on the Gemini North 8 m telescope. Using recent data from the Cassini/Huygens mission on the atmospheric composition and surface and aerosol properties, we develop a multiple-scattering radiative transfer model for the Titan atmosphere. The Titan spectrum at these wavelengths is dominated by absorption due to methane with a series of strong absorption band systems separated by window regions where the surface of Titan can be seen. We use a line-by-line approach to derive the methane absorption coefficients. The methane spectrum is only accurately represented in standard line lists down to ∼2.1 μm. However, by making use of recent laboratory data and modeling of the methane spectrum we are able to construct a new line list that can be used down to 1.3 μm. The new line list allows us to generate spectra that are a good match to the observations at all wavelengths longer than 1.3 μm and allow us to model regions, such as the 1.55 μm window that could not be studied usefully with previous line lists such as HITRAN 2008. We point out the importance of the far-wing line shape of strong methane lines in determining the shape of the methane windows. Line shapes with Lorentzian, and sub-Lorentzian regions are needed to match the shape of the windows, but different shape parameters are needed for the 1.55 μm and 2 μm windows. After the methane lines are modeled our observations are sensitive to additional absorptions, and we use the data in the 1.55 μm region to determine a D/H ratio of 1.77 ± 0.20 × 10−4, and a CO mixing ratio of 50 ± 11 ppmv. In the 2 μm window we detect absorption features that can be identified with the ν5 + 3ν6 and 2ν3 + 2ν6 bands of CH3D.  相似文献   

19.
The S(1) line of the pressure-induced fundamental band of H2 was identified and measured in the spectra of Saturn and Jupiter. This broad line at 4750 cm?1 lies in a region free from telluric and planetary absorptions. It is about 99% absorbing in the core; the high-frequency wing extends to at least 5100 cm?1. We compare the obseved line shape to the predictions of both a reflecting-layer model (RLM) and a homogeneous scattering model (HSM). The RLM provides a good fit to the Saturn line profile for temperatures near 150K; the derived base-level density is 0.52 (+0.26, ?0.17) amagat and the H2 abundance is 25 (+10, ?9) km-amagat, assuming a scale height of 48 km. The Jupiter line profile is fit by both the RLM and HSM, but for widely differing temperatures, neither of which seems probable. The precise fitting of the observed S(1) line profile to computed models depends critically on the determination of the true continuum level; difficulties encountered in finding the continuum, especially for Jupiter, are discussed. Derived RLM densities and abundances for both planets are substantially lower than those derived from RLM analyses of the H2 quadrupole lines, the 3ν3 band of CH4, and from other sources.  相似文献   

20.
W. Macy 《Icarus》1980,41(1):153-158
Matching computed spectra for the ν4 band of methane, the ν9 band of ethane, and the R branch of the ν5 band of acetylene to observed spectra for Neptune suggests mixing ratios of CH4/H2 ～ 10?3?10?2, C2H6/H2 ～ 10?6, and C2H2/H2 ～ 10?8 in the stratosphere.  相似文献   

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