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1.
Observations of H2O rotational lines from the Infrared Space Observatory (ISO) and the Submillimeter Wave Astronomy Satellite (SWAS) and of the CO2 ν2 band by ISO are analyzed jointly to determine the origin of water vapor and carbon dioxide in Jupiter's stratosphere. Simultaneous modelling of ISO/LWS and ISO/SWS observations acquired in 1997 indicates that most of the stratospheric jovian water is restricted to pressures less than 0.5±0.2 mbar, with a disk-averaged column density of (2.0±0.5)×1015 cm−2. Disk-resolved observations of CO2 by ISO/SWS reveal latitudinal variations of the CO2 abundance, with a decrease of at least a factor of 7 from mid-southern to mid-northern latitudes, and a disk-center column density of (3.4±0.7)×1014 cm−2. These results strongly suggest that the observed H2O and CO2 primarily result from the production, at midsouthern latitudes, of oxygenated material in the form of CO and H2O by the Shoemaker-Levy 9 (SL9) impacts in July 1994 and subsequent chemical and transport evolution, rather than from a permanent interplanetary dust particle or satellite source. This conclusion is supported by quantitative evolution model calculations. Given the characteristic vertical mixing times in Jupiter's stratosphere, material deposited at ∼0.1 mbar by the SL9 impacts is indeed expected to diffuse down to the ∼0.5 mbar level after 3 years. A coupled chemical-horizontal transport model indicates that the stability of water vapor against photolysis and conversion to CO2 is maintained over typically ∼50 years by the decrease of the local CO mixing ratio associated with horizontal spreading. A model with an initial (i.e., SL9-produced) H2O/CO mass mixing ratio of 0.07, not inconsistent with immediate post-impact observations, matches the observed H2O abunda nce and CO2 horizontal distribution 3 years after the impacts. In contrast, the production of CO2 from SL9-produced CO and a water component deriving from an interplanetary dust component is insufficient to account for the observed CO2 amounts. The observations can further be used to place a stringent upper limit (8×104 cm−2 s−1) on the permanent water influx into Jupiter. This may indicate that the much larger flux observed at Saturn derives dominantly from a ring source, or that the ablation of micrometeoroids leads dominantly to different species at Saturn (H2O) and Jupiter (CO). Finally, the SWAS H2O spectra do not appear fully consistent with the ISO data and should be confirmed by future ODIN and Herschel observations.  相似文献   

2.
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 (LS=331°.17 until LS=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 LS ranges: 331-360°, 0-30° and 30-52°. For the first LS 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 LS 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 LS=331-360°, thus confirming the effect of seasonal condensation of CO2 on the north polar cap, but we have no agreement for other seasons.  相似文献   

3.
Venus was observed at 2.4 and 3.7 μm with a resolving power of 4×104 using the long-slit high-resolution spectrograph CSHELL at NASA IRTF. The observations were made along a chord that covered a latitude range of ± 60° at a local time near 8:00. The continuous reflectivity and limb brightening at 2.4 μm are fitted by the clouds with a single scattering albedo 1−a=0.01 and a pure absorbing layer with τ=0.09 above the clouds. The value of 1−a agrees with the refractive index of H2SO4 (85%) and the particle radius of 1 μm. The absorbing layer is similar to that observed by the UV spectrometer at the Pioneer Venus orbiter. However, its nature is puzzling. CO2 was measured using its R32 and R34 lines. The retrieved product of the CO2 abundance and airmass is constant at 1.9 km-atm along the instrument slit in the latitude range of ± 60°. The CO mixing ratio (measured using the P21 line) is rather constant at 70 ppm, and its variations of ∼10% may be caused by atmospheric dynamics. The observed value is higher than the 50 ppm retrieved previously from a spectrum of the full disk, possibly, because of some downward extension of the mesospheric morningside bulge of CO. The observations of the HF R3 line reveal a constant HF mixing ratio of 3.5±0.5 ppb within ± 60° of latitude, which is within the scatter in the previous measurements of HF. OCS has been detected for the first time at the cloud tops by summing 17 lines of the P-branch. The previous detections of OCS refer to the lower atmosphere at 30-35 km. The retrieved OCS mixing ratio varies with a scale height of 1 to 3 km. The mean OCS mixing ratio is ∼2 ppb at 70 km and ∼14 ppb at 64 km. Vertical motions in the atmosphere may change the OCS abundance. The detected OCS should significantly affect Venus' photochemistry. A sensitive search for H2S using its line at 2688.93 cm−1 results in a 3 sigma upper limit of 23 ppb, which is more restrictive than the previous limit of 100 ppb.  相似文献   

4.
A large number of spectra measured by the planetary Fourier spectrometer aboard the European Mars Express mission have been studied to identify the average properties of methane in the Martian atmosphere. Using the line at 3018 cm−1, we have studied the seasonal, diurnal, and spatial variations of methane through the analysis of large averages of spectra (more than 1000 measurements). Methane mixing ratio has been obtained simultaneously with water vapour mixing ratio and water ice content, by best fitting (minimising the χ2) the computed averages with synthetic spectra. These spectra were computed for different values of the three parameters (methane and water vapour mixing ratio, and water ice optical depth).The methane mixing ratio shows a slow decrease from northern spring to southern summer with an average value of 14±5 ppbv (part per billion by volume) and it does not show a particular trend with latitude. The methane mixing ratio seems not to be uniform in longitude in the Martian atmosphere, as already reported by Formisano et al. [2004. Detection of methane in the atmosphere of Mars. Science 306, 1758-1761]. Two maxima are present at −40°E and +70°E longitude. In local time, the methane mixing ratio seems to follow the water vapour diurnal cycle. The most important point for future understanding is, however, that there are special orbits in which methane mixing ratio has a very high value.  相似文献   

5.
Ethane (C2H6), methylacetylene (CH3C2H or C3H4) and diacetylene (C4H2) have been discovered in Spitzer 10-20 μm spectra of Uranus, with 0.1-mbar volume mixing ratios of (1.0±0.1)×10−8, (2.5±0.3)×10−10, and (1.6±0.2)×10−10, respectively. These hydrocarbons complement previously detected methane (CH4) and acetylene (C2H2). Carbon dioxide (CO2) was also detected at the 7-σ level with a 0.1-mbar volume mixing ratio of (4±0.5)×10−11. Although the reactions producing hydrocarbons in the atmospheres of giant planets start from radicals, the methyl radical (CH3) was not found in the spectra, implying much lower abundances than in the atmospheres of Saturn or Neptune where it has been detected. This finding underlines the fact that Uranus' atmosphere occupies a special position among the giant planets, and our results shed light on the chemical reactions happening in the absence of a substantial internal energy source.  相似文献   

6.
We have investigated the abundances of Titan's stratospheric oxygen compounds using 0.5 cm−1 resolution spectra from the Composite Infrared Spectrometer on the Cassini orbiter. The CO abundance was derived for several observations of far-infrared nadir spectra, taken at a range of latitudes (75° S-35° N) and emission angles (0°-60°), using rotational lines that have not been analysed before the arrival of Cassini at Saturn. The derived volume mixing ratios for the different observations are mutually consistent regardless of latitude. The weighted mean CO volume mixing ratio is 47±8 ppm if CO is assumed to be uniform with latitude. H2O could not be detected and an upper limit of 0.9 ppb was determined. CO2 abundances derived from mid-infrared nadir spectra show no significant latitudinal variations, with typical values of 16±2 ppb. Mid-infrared limb spectra at 55° S were used to constrain the vertical profile of CO2 for the first time. A vertical CO2 profile that is constant above the condensation level at a volume mixing ratio of 15 ppb reproduces the limb spectra very well below 200 km. This is consistent with the long chemical lifetime of CO2 in Titan's stratosphere. Above 200 km the CO2 volume mixing ratio is not well constrained and an increase with altitude cannot be ruled out there.  相似文献   

7.
The J = 3-2 rotational line of CO in Neptune has been measured using the heterodyne receiver B3 at the JCMT. The spectral resolution was 1.25 MHz and 25 tunings were used to cover a frequency range of almost 20 GHz. The measured line shape, encompassing both the broad absorption feature arising in the lower atmosphere and a narrow emission core from the upper stratosphere, indicates that the CO mole ratio is not uniform with altitude, with best-fit values of in the upper stratosphere and 0.6±0.4×10−6 in the lower stratosphere and troposphere. The higher stratospheric abundance indicates that a dual, internal and external, origin of CO is most likely.  相似文献   

8.
Thirteen lines of the CO band near 4.7 μm have been observed on a jovian hot spot at a resolution of 0.045 cm−1. The measured line profiles indicate that the CO mole fraction is 1.0±0.2 ppb around the 6-bar level and is larger in the upper troposphere and/or stratosphere. An external source of CO providing an abundance of 4+3−2×1016 molecules cm−2 is implied by the observations in addition to the amount deposited at high altitude by the Shoemaker-Levy 9 collision. From a simple diffusion model, we estimate that the CO production rate is (1.5-10)×106 molecules cm−2 s−1 assuming an eddy diffusion coefficient around the tropopause between 300 and 1500 cm2 s−1. Precipitation of oxygen atoms from the jovian magnetosphere or photochemistry of water vapor from meteoroidal material can only provide a negligible contribution to this amount. A significant fraction of the CO in Jupiter's upper atmosphere may be formed by shock chemistry due to the infall of kilometer- to subkilometer-size Jupiter family comets. Using the impact rate from Levison et al. (2000, Icarus143, 415-420) rescaled by Bottke et al. (2002, Icarus156, 399-433), this source can provide the observed stratospheric CO only if the eddy diffusion coefficient around the tropopause is 100-300 cm2 s−1. Higher values, ∼700 cm2 s−1, would require an impact rate larger by a factor of 5-10, which cannot be excluded considering uncertainties in the distribution of Jupiter family comets. Such a large rate is indeed consistent with the observed cratering record of the Galilean satellites (Zahnle et al. 1998, Icarus136, 202-222). On the other hand, the ∼1 ppb concentration in the lower troposphere requires an internal source. Revisiting the disequilibrium chemistry of CO in Jupiter, we conclude that rapid vertical mixing can provide the required amount of CO at ∼6 bar for a global oxygen abundance of 0.2-9 times the solar value considering the uncertainties in the convective mixing rate and in the chemical constants.  相似文献   

9.
Variations of the upper cloud boundary and the CO, HF, and HCl mixing ratios were observed using the CSHELL spectrograph at NASA IRTF. The observations were made in three sessions (October 2007, January 2009, and June 2009) at early morning and late afternoon on Venus in the latitude range of ±60°. CO2 lines at 2.25 μm reveal variations of the cloud aerosol density (∼25%) and scale height near 65 km. The measured reflectivity of Venus at low latitudes is 0.7 at 2.25 μm and 0.028 at 3.66 μm, and the effective CO2 column density is smaller at 3.66 μm than those at 2.25 μm by a factor of 4. This agrees with the almost conservative multiple scattering at 2.25 μm and single scattering in the almost black aerosol at 3.66 μm. The expected difference is just a factor of (1 − g)−1 = 4, where g = 0.75 is the scattering asymmetry factor for Venus’ clouds. The observed CO mixing ratio is 52 ± 4 ppm near 08:00 and 40 ± 4 ppm near 16:30 at 68 km, and the higher ratio in the morning may be caused by extension of the CO morningside bulge to the cloud tops. The observed weak limb brightening in CO indicates an increase of the CO mixing ratio with altitude. HF is constant at 3.5 ± 0.2 ppb at 68 km in both morningside and afternoon observations and in the latitude range ±60°. Therefore the observations do not favor a bulge of HF, though HF is lighter than CO. Probably a source in the upper atmosphere facilitates the bulge formation. The recent measurements of HCl near 70 km are controversial (0.1 and 0.74 ppm) and require either a strong sink or a strong source of HCl in the clouds. The HCl lines of the (2-0) band are blended by the solar and telluric lines. Therefore we observed the P8 lines of the (1-0) band at 3.44 μm. These lines are spectrally clean and result in the HCl mixing ratio of 0.40 ± 0.03 ppm at 74 km. HCl does not vary with latitude within ±60°. Our observations support a uniformly mixed HCl throughout the Venus atmosphere.  相似文献   

10.
Submillimeter line observations of CO in the Venus middle atmosphere (mesosphere) were observed with the James Clerk Maxwell Telescope (JCMT, Mauna Kea) about the May 2000, February 2002 superior and July 1999, March 2001 inferior conjunctions of Venus. Combined 12CO and 13CO isotope spectral line measurements at 345 and 330 gHz frequencies, respectively, provided enhanced sensitivity and vertical coverage for simultaneous retrievals of atmospheric temperatures and CO mixing ratios over the altitude region 75-105 km with vertical resolution 4-5 km. Supporting millimeter 12CO spectral line observations with the Kitt Peak 12-m telescope (Steward Observatories) provide enhanced temporal coverage and CO mixing sensitivity. Implementation of CO/temperature profile retrievals for the 2000, 2002 dayside (superior conjunction) and 1999, 2001 nightside (inferior conjunction) periods yields a first-time definition of the vertical structure and diurnal variation of a low-to-mid-latitude mesopause within the Venus atmosphere. At the times of these 1999-2002 observations, the Venus mesopause was located at a slightly lower level in the nightside (0.5 mbar, ∼87 km) versus the dayside (0.2 mbar, ∼91 km) atmosphere. Average diurnal variation of Venus mesospheric temperatures appears to be ≤ 5 K at and below the mesopause. Diurnal variation of Venus thermospheric temperatures increases abruptly just above the mesopause, reaching 50 K by the 0.01-mbar pressure level (∼102 km). Atmospheric temperatures above and below the Venus mesopause exhibited global-scale (≥4000 km horizontal) variations of large amplitude (7-15 K) on surprisingly short timescales (daily to monthly) during the 2001 nightside and 2002 dayside observing periods. Venus dayside mesospheric temperatures observed during the 2002 superior conjunction were also 10-15 K warmer than observed during the 2000 superior conjunction. A characteristic timescale for these global temperature variations is not defined, but their magnitude is comparable to previous determinations of secular variability in nightside mesospheric temperatures (Clancy and Muhleman, 1991).  相似文献   

11.
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.  相似文献   

12.
The apparition of Comet C/1996 B2 (Hyakutake) offered an unexpected and rare opportunity to probe the inner atmosphere of a comet with high spatial resolution and to investigate with unprecedented sensitivity its chemical composition. We present observations of over 30 submillimeter transitions of HCN, H13CN, HNC, HNCO, CO, CH3OH, and H2CO in Comet Hyakutake carried out between 1996 March 18 and April 9 at the Caltech Submillimeter Observatory. Detections of the H13CN (4–3) and HNCO (160,16–150,15) transitions represent the first observations of these species in a comet. In addition, several other transitions, including HCN (8–7), CO (4–3), and CO (6–5) are detected for the first time in a comet as is the hyperfine structure of the HCN (4–3) line. The observed intensities of the HCN (4–3) hyperfine components indicate a line center optical depth of 0.9 ± 0.2 on March 22.5 UT. The HCN/HNC abundance ratio in Comet Hyakutake at a heliocentric distance of 1 AU is similar to that measured in the Orion extended ridge— a warm, quiescent molecular cloud. The HCN/H13CN abundance ratio implied by our observations is 34 ± 12, similar to that measured in giant molecular clouds in the galactic disk but significantly lower than the Solar System12C/13C ratio. The low HCN/H13CN abundance ratio may be in part due to contamination by an SO2line blended with the H13CN (4–3) line. In addition, chemical models suggest that the HCN/H13CN ratio can be affected by fractionation during the collapse phase of the protosolar nebula; hence a low HCN/H13CN ratio observed in a comet is not inconsistent with the solar system12C/13C isotopic ratio. The abundance of HNCO relative to water derived from our observations is (7 ± 3) × 10−4. The HCN/HNCO abundance ratio is similar to that measured in the core of Sagittarius B2 molecular cloud. Although a photo-dissociative channel of HNCO leads to CO, the CO produced by HNCO is a negligible component of cometary atmospheres. Production rates of HCN, CO, H2CO, and CH3OH are presented. Inferred molecular abundances relative to water are typical of those measured in comets at 1 AU from the Sun. The exception is CO, for which we derive a large relative abundance of 30%. The evolution of the HCN production rate between March 20 and March 30 suggests that the increased activity of the comet was the cause of the fragmentation of the nucleus. The time evolution of the H2CO emission suggests production of this species from dust grains.  相似文献   

13.
We report on mid-resolution (R∼2000) spectroscopic observations of Titan, acquired in November 2000 with the Very Large Telescope and covering the range 4.75-5.07 μm. These observations provide a detailed characterization of the CO (1-0) vibrational band, clearly separating for the first time individual CO lines (P10 to P19 lines of 13CO). They indicate that the CO/N2 mixing ratio in Titan’s troposphere is 32±10 ppm. Comparison with photochemical models indicates that CO is not in a steady state in Titan’s atmosphere. The observations confirm that Titan’s 5-μm continuum geometric albedo is ∼0.06, and further indicates a ∼20% albedo decrease over 4.98-5.07 μm. Nonzero flux is detected at the 0.01 geometric albedo level in the saturated core of the 12CO (1-0) band, at 4.75-4.85 μm, providing evidence for backscattering on the stratospheric haze. Finally, emission lines are detected at 4.75-4.835 μm, coinciding in position with lines from the CO(1-0) and/or CO(2-1) bands. Matching them by thermal emission would require Titan’s stratosphere to be much warmer (by ∼ 25 K at 0.1 mbar) than indicated by the methane 7.7-μm emission and the Voyager radio-occultation. We show instead that a nonthermal mechanism, namely solar-excited fluorescence, is a more plausible source for these emissions. Improved observations and laboratory measurements on the vibrational-translational relaxation of CO are needed for further interpretation of these emissions in terms of a CO stratospheric mixing ratio.  相似文献   

14.
A. Tokunaga  R.D. Cess 《Icarus》1977,32(3):321-327
A model for the temperature inversion within the atmosphere of Saturn is proposed and is shown to be consistent with photometric data in the 17- to 25-μm region. The proposed model incorporates solar heating by some “aerosol,” with the aerosol heating per unit mass of the atmosphere being uniformly distributed throughout that portion of the atmosphere overlying the upper cloud deck. For a methane-to-hydrogen mixing ratio of 7 × 10?4, the model results suggest that 20% of the incident solar radiation is absorbed by the aerosol, while this is reduced to 16% for an enhanced methane mixing ratio of 2.1 × 10?3.  相似文献   

15.
The Venus mesosphere constitutes a highly variable transition region between the zonal rotation of the lower atmosphere and the diurnal circulation of the upper atmosphere. It further serves as the primary photochemical region of the Venus atmosphere. We obtained James Clerk Maxwell Telescope (JCMT, Mauna Kea Hawaii) sub-millimeter line observations of mesospheric 12CO and 13CO during coordinated space (MESSENGER and Venus Express) and ground-based observations of Venus in June of 2007. Such CO spectra line measurements support temperature, CO mixing ratio, and wind retrievals over the 80-110 km altitude range, encompassing the upper mesosphere and lower thermosphere of Venus. Five-point beam integrations were obtained across the observed Venus disk, allowing distinction of afternoon (noon to 6 p.m.) versus evening (6 p.m. to midnight) local times and northern (0-60N) versus southern (0-60S) latitudes. Distinctive diurnal variations (noon to midnight) are retrieved for both temperatures above 95 km and CO mixing ratios above 85 km altitudes. Separate CO line maps obtained on (UT) June 2, 3, 6, and 11 indicate moderate daily variability in afternoon and evening CO mixing ratios (20-50%) and temperatures (5-10 K). Average Venus mesospheric temperatures over this period were 10 K warmer than returned from 1978 to 1979 Pioneer Venus or 2000-01 sub-millimeter measurements, without evidence for the very large temperature inversions indicated by Venus Express SPICAV measurements at 90-100 km altitudes (Bertaux, J.L., Vandaele, A.-C., Korablev, O., Villard, E., Fedorova, A., Fussen, D., Quémerais, E., Belyaev, D., Mahieux, A., Montmessin, F., Muller, C., Neefs, E., Nevejans, D., Wilquet, V., Dubois, J.P. Hauchecorne, A., Stepanov, A., Vinogradov, I., Rodin, A., Bertaux, J.-L., Nevejans, D., Korablev, O., Montmessin, F., Vandaele, A.-C., Fedorova, A., Cabane, M., Chassefière, E., Chaufray, J.Y., Dimarellis, E., Dubois, J.P., Hauchecorne, A., Leblanc, F., Lefèvre, F., Rannou, P., Quémerais, E., Villard, E., Fussen, D., Muller, C., Neefs, E., Van Ransbeeck, E., Wilquet, V., Rodin, A., Stepanov, A., Vinogradov, I., Zasova, L., Forget, F., Lebonnois, S., Titov, D., Rafkin, S., Durry, G., Gérard, J.C., Sandel, B., 2007. A warm layer in Venus’ cryosphere and high-altitude measurements of HF, HCl, H2O and HDO. Nature 450, 646-649). Measured Doppler shifts associated with June 2 and 11 12CO line center absorptions indicate nearly supersonic (200 m/s, Mach 1) afternoon-to-evening (retrograde) circulation; composed of additive subsolar-to-antisolar (SSAS) and zonal retrograde wind components, which are not separable due to the particular observational geometry.  相似文献   

16.
The detection of CH4 in the martian atmosphere, at a mixing ratio of about 10 ppb, prompted Krasnopolsky et al. [Krasnopolsky, V.A., Maillard, J.P., Owen, T.C., 2004. Icarus 172, 537-547] and Krasnopolsky [Krasnopolsky, V.A., 2006. Icarus 180, 359-367] to propose that the CH4 is of biogenic origin. Bar-Nun and Dimitrov [Bar-Nun, A., Dimitrov, V., 2006. Icarus 181, 320-322] proposed that CH4 can be formed in the martian atmosphere by photolysis of H2O in the presence of CO. We based our arguments on a clear demonstration that CH4 is formed in our experiments, and on thermodynamic equilibrium calculations, which show that CH4 formation is favored even in the presence of oxygen at a mixing ratio 1.3×10−3, as observed on Mars. In the present comment, Krasnopolsky [Krasnopolsky, V.A., 2007. Icarus, in press (this issue)] presents his arguments against the suggestion of Bar-Nun and Dimitrov [Bar-Nun, A., Dimitrov, V., 2006. Icarus 181, 320-322], based on the effect of O2 on CH4 formation, the absence of kinetic pathways for CH4 formation and on the inadequacy of thermodynamic equilibrium calculations to describe the martian atmosphere. In this rebuttal we demonstrate that experiments with molecular oxygen at a ratio of O2/CO2=(8.9-17)×10−3, exceeding the martian ratio, still form CH4. Thermodynamic equilibrium calculations replicate the experimental CH4 mixing ratio to within a factor of 1.9 and demonstrate that CH4 production is favored in the martian atmosphere, which is obviously not in thermodynamic equilibrium. Consequently, we do not find the presence of methane to be a sign of biological activity on Mars.  相似文献   

17.
We present an analysis of observations of the auroral/polar regions of Saturn, carried out in 1999, 2004 and 2005, making use of the facility spectrometer, CGS4, on the United Kingdom Infrared Telescope (UKIRT), Mauna Kea, Hawaii. We obtain temperatures of 380(±70) K in 1999 and 420(±70) K in 2004. (The 2005 data has insufficient spectral resolution for a temperature determination to be made.) Our most probable interpretation is that the temperature of Saturn's auroral/polar H+3 layer should be taken as 400(±50) K. This is lower than the value obtained by Miller et al. [Miller, S., and 10 colleagues, 2000. Philos. Trans. R. Soc. 358, 2485-2502], which is shown to be in error. Our analysis reveals clearly that the line emission due to H+3 varies considerably, showing nearly an order of magnitude increase when one compares the data obtained in 1999 with those of 2004. Our conclusion is that this variability is (mainly) due to the changing H+3 column density. By analogy with modelling results obtained for Jupiter, we estimate that the particle (keV electron) precipitation experienced by Saturn must be ∼20 times greater in 2004 than in 1999, to produce this additional ionisation. The H+3 emission increases, but this is insufficient to offset most of the heating due to the extra particle precipitation, indicating that this ion does not act as a “thermostat” on Saturn, in the same way that it does on Jupiter.  相似文献   

18.
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.  相似文献   

19.
Jeremy Bailey 《Icarus》2009,201(2):444-453
The discovery of the near infrared windows into the Venus deep atmosphere has enabled the use of remote sensing techniques to study the composition of the Venus atmosphere below the clouds. In particular, water vapor absorption lines can be observed in a number of the near-infrared windows allowing measurement of the H2O abundance at several different levels in the lower atmosphere. Accurate determination of the abundance requires a good database of spectral line parameters for the H2O absorption lines at the high temperatures (up to ∼700 K) encountered in the Venus deep atmosphere. This paper presents a comparison of a number of H2O line lists that have been, or that could potentially be used, to analyze Venus deep atmosphere water abundances and shows that there are substantial discrepancies between them. For example, the early high-temperature list used by Meadows and Crisp [Meadows, V.S., Crisp, D., 1996. J. Geophys. Res. 101 (E2), 4595-4622] had large systematic errors in line intensities. When these are corrected for using the more recent high-temperature BT2 list of Barber et al. [Barber, R.J., Tennyson, J., Harris, G.J., Tolchenov, R.N., 2006. Mon. Not. R. Astron. Soc. 368, 1087-1094] their value of 45±10 ppm for the water vapor mixing ratio reduces to 27±6 ppm. The HITRAN and GEISA lists used for most other studies of Venus are deficient in “hot” lines that become important in the Venus deep atmosphere and also show evidence of systematic errors in line intensities, particularly for the 8000 to 9500 cm−1 region that includes the 1.18 μm window. Water vapor mixing ratios derived from these lists may also be somewhat overestimated. The BT2 line list is recommended as being the most complete and accurate current representation of the H2O spectrum at Venus temperatures.  相似文献   

20.
These are the first results from nadir studies of meridional variations in the abundance of stratospheric acetylene and ethane from Cassini/CIRS data in the southern hemisphere of Saturn. High resolution, 0.5 cm−1, CIRS data was used from three data sets taken in June-November 2004 and binned into 2° wide latitudinal strips to increase the signal-to-noise ratio. Tropospheric and stratospheric temperatures were initially retrieved to determine the temperature profile for each latitude bin. The stratospheric temperature at 2 mbar increased by 14 K from 9° to 68° S, including a steep 4 K rise between 60° and 68° S. The tropospheric temperatures showed significantly more meridional variation than the stratospheric ones, the locations of which are strongly correlated to that of the zonal jets. Stratospheric acetylene abundance decreases steadily from 30 to 68° S, by a factor of 1.8 at 2.0 mbar. Between 18° and 30° S the acetylene abundance increases at 2.0 mbar. Global values for acetylene have been calculated as (1.9±0.19)×10−7 at 2.0 mbar, (2.6±0.27)×10−7 at 1.6 mbar and (3.1±0.32)×10−7 at 1.4 mbar. Global values for ethane are also determined and found to be (1.6±0.25)×10−5 at 0.5 mbar and (1.4±0.19)×10−5 at 1.0 mbar. Ethane abundance in the stratosphere increases towards the south pole by a factor of 2.5 at 2.0 mbar. The increase in stratospheric ethane is especially pronounced polewards of 60° S at 2.0 mbar. The increase of stratospheric ethane towards the south pole supports the presence of a meridional wind system in the stratosphere of Saturn.  相似文献   

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