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1.
H. Levy 《Planetary and Space Science》1973,21(4):575-591
Altitude profiles for the number densities of NO, NO2, NO3, N2O5, HNO2, CH3O, CH3O2, H2CO, OH, and HO2 are calculated as a function of time of day with a steady-state photochemical model in which the altitude profiles for the number densities of H2O, CH4, H2, CO, O3, and the sum of NO and NO2 are fixed at values appropriate to a summer latitude of 34°. Average daily profiles are calculated for the long-lived species, HNO3, H2O2, and CH3O2H.The major nitrogen compound HNO3 may have a number density approaching 5 × 1011 molecules cm?3 at the surface, although an effective loss path due to collisions with particulates could greatly reduce this value.The number density of OH remains relatively unchanged in the first 6 km and reaches 1 × 107 molecules cm?3 at noon, while the number density of HO2 decreases throughout the lower troposphere from its noontime value of 8 × 108 molecules cm?3 at the surface.H2O2 and H2CO both have number densities in the ppb range in the lower troposphere.Owing to decreasing temperature and water concentration, the production of radicals and their steady-state number densities decrease with altitude, reaching a noontime minimum of 1 × 108 molecules cm?3 for OH and 3 × 107 molecules cm?3 for HO2 at the tropopause. The related minor species show even sharper decreases with increasing altitude.The primary path for interconverting OH and HO2 serves as the major sink for CO and leads to a tropospheric lifetime for CO of ~0.1 yr.Another reaction cycle, the oxidation of CH4, is quite important in the lower troposphere and leads to the production of H2CO along with the destruction of CH4 for which a tropospheric lifetime of ~2 yr is estimated.The destruction of H2CO that was produced in the CH4 oxidation cycle provides the major source of CO and H2 in the atmosphere. 相似文献
2.
The methane abundance in the lower Jovian stratosphere is measured using Galilean satellite eclipse light curves. Spectrally selective observations in and between absorption bands are compared. An average mixing ratio at the locations measured is [CH4]/[H2] ～ 1.3 × 10?3, larger than the value 0.9 × 10?3 expected for a solar abundance of carbon. Some zenographic variation of the mixing ratio may occur. Observationally compatible values are 1.3–2.0 × 10?3 in the STZ, 1.3– 2.6 × 10?3 on the GRS/STrZ edge, and 0.7–1.3 × 10?3 in the GRS. 相似文献
3.
The abundances of PH3, CH3D, and GeH4 are derived from the 2100- to 2250-cm?1 region of the Voyager 1 IRIS spectra. No evidence is seen for large-scale variations of the phosphine abundance over Jovian latitudes between ?30 and +30°. In the atmospheric regions corresponding to 170–200°K, the derived PH3/H2 value is (4.5 ± 1.5) × 10?7 or 0.75 ± 0.25 times the solar value. This result, compared with other PH3 determinations at 10 μm, suggests than the PH3/H2 ratio on Jupiter decreases with atmospheric pressure. In the 200–250°K region, we derive, within a factor of 2, CH3D/H2 and GeH4/H2 ratios of 2.0 × 10?7 and 1.0 × 10?9, respectively. Assuming a C/H value of 1.0 × 10?3, as derived from Voyager, our CH3D/H2 ratio implies a D/H ratio of 1.8 × 10?5, in reasonable agreement with the interstellar medium value. 相似文献
4.
A variety of models are explored to study the photochemistry of CO2 in the Martian atmosphere with emphasis on reactions involving compounds of carbon, hydrogen, and oxygen. Acceptable models are constrained to account for measured concentrations of CO and O above 90 km, with an additional requirement that they should be in accord with observations of CO, O2, and O3 in the lower atmosphere. Dynamical mixing must be exceedingly rapid at altitudes above 90 km, with effective eddy diffusion coefficients in excess of 107 cm2 sec?1. If recombination of CO2 is to occur mainly by gas phase chemistry, catalyzed by trace quantities of H, OH, and HO2, mixing must be rapid over the altitude interval 30 to 40 km. The value implied for the diffusion coefficient in this region is a function of assumptions made regarding the rates for reaction of OH with HO2 to form H2O and of the rate for reaction of HO2 with itself to form H2O2. If rates for these reactions are taken to have values similar to rates used in current models for the Earth's stratosphere, the eddy diffusion coefficient at 40 km on Mars should be about 5 × 107 cm2 sec?1, consistent with Zurek's (1976) estimate for this parameter inferred from tidal theory. Surface chemistry could have an influence on the abundances of atmospheric CO and O2, but a major effect would imply sluggish mixing at all altitudes below 50 km and in addition would carry implications for the magnitude of the rates for reaction of OH with HO2 and HO2 with itself. 相似文献
5.
The scattering and absorption properties of Axel dust were investigated by means of Mie theory. We find that a flat distribution of particle radii between 0 and 0.1 μm, and an imaginary part of the index of refraction which varies as λ?2.5 produce a good fit to the variation of Titan's geometric albedo with wavelength (λ) provided that τext, the extinction optical depth of Titan's atmosphere at 5000 Å, is about 10. The real part of the complex index is taken to be 2.0. The model assumes that the mixing ratio of Axel dust to gas is uniform above the surface of Titan. The same set of physical properties for Axel dust also produces a good fit to Saturn's albedo if τext = 0.7 at 5000 Å. To match the increase in albedo shortward of 3500 Å, a clear layer (containing about 7 km-am H2) is required above the Axel dust. Such a layer is also required to explain the limb brightening in the ultraviolet. These models can be used to analyze the observed equivalent widths of the visible methane bands. The analysis yields an abundance of the order of 1000 m-am CH4 in Titan's atmosphere. The derived CH4/H2 mixing ratio for Saturn is about 3.5 × 10?3 or an enhancement of about 5 over the solar ratio. 相似文献
6.
The abundance of H2O is derived from the 1900- to 2100-cm?1 region of the Voyager 1 IRIS spectra. Scale variations of about a factor of 2 are seen in the water abundance between the North and South Equatorial Belts. Averaged over the full disk, the mixing ratio is , if H2O is uniformly mixed in the atmospheric region having temperatures of 230 to 270°K; this result implies a solar depletion by a factor of 100 in this region. In the belts, the best agreement is obtained for a H2O/H2 mixing ratio of 4.0 × 10?6 in the NEB and 7.2 × 10?6 in the SEB, assuming a constant mixing ratio. 相似文献
7.
Nonthermal escape processes responsible for the escape of hydrogen and deuterium from Venus are examined for present and past atmospheres. Three mechanisms are important for the escape of hydrogen from the present atmosphere: (a) charge exchange of plasmaspheric H+ with exospheric H, (b) impact of exospheric hot O atoms on H, and (c) ion molecule reactions involving O+ and H2. However, in the past when the H abundance was higher, the charge-exchange mechanism would be the strongest. The H escape flux increases rapidly with increasing hydrogen abundance in the upper atmosphere and saturates at a value of 1 × 1010 cm?2 sec?1 emerging primarily from the day side when the H mixing ratio at the homopause is 2 × 10?3. This corresponds to an H2O mixing ratio of 1 × 10?3 at the cold trap and ～15% at the surface. Deuterium would also escape by the charge-exchange mechanism and a D/H enrichment by a factor of ～1000 over the nonthermal escape regime is expected, which could have lasted over the last 3 billion years. Coincidentally, the onset of hydrodynamic flow leading to efficient H escape occurs just at the H2O mixing ratio at which the charge-exchange escape flux saturates. Thus it is possible that Venus has lost an Earth-equivalent ocean of water over geologic time. If so, either the D/H enrichment has been kept low by modest outgassing of juvenile water or Venus started out with a D/H ratio of ～4.0 × 10?6. 相似文献
8.
The radiative lifetimes of cometary OH are calculated as a function of the heliocentric velocity of the comet and the velocity distributions of the product atoms are determined. At a distance of 1 AU from the Sun, the lifetimes vary between 1.2×105 and 1.9×105 sec at solar minimum and between 1.0×105 and 1.4×105 sec at solar maximum, depending upon velocity. Continuous absorption into the repulsive 12Σ- state is major destruction path. The calculated lifetimes are generally consistent with the lifetimes inferred from observations, but suggest some elaboration of the models is necessary. Photodissociation of OH produces a low-velocity component of hydrogen atoms at 8 km sec?1 relative to the parent OH molecule and a high-velocity component between 17 and 27 km sec?1. Photodissociation of OH leads to metastable O(1D) and O(1S) and is an additional source of the red and green line emission of atomic oxygen. The lifetime of OD is estimated to be about 4.3× 105 sec at solar minimum and 2.6×105 sec at solar maximum so that the OD/OH ratio in comets is enhanced relative to the HDO/H2O production ratio by a factor between 2 and 3. Photodissociation of OD produces only high-velocity D atoms with a mean value of 17 km sec?1. 相似文献
9.
William C. Maguire 《Icarus》1977,32(1):85-97
The Mariner 9 infrared spectrometer obtained data over a large part of Mars for almost a year beginning late in 1971. Mars' infrared emission spectrum was measured from 200 to 2000 cm?1 with an apodized resolution of 2.4 cm?1. No significant deviation from terrestrial ratios of carbon (12C/13C) or oxygen (16O/18O; 16O/17O) isotopes was observed on Mars. The 12C/13C isotopic ratio was found to be terrestrial with an uncertainty of 15%. Upper limits have been calculated for several minor constituents. With an effective noise equivalent radiance of 1.2 × 10?9 W cm?2 sr?1/cm?1, new upper limits in centimeter-atmospheres of 2 × 10?5 for C2H2, 4 × 10?3 for C2H4, 3 × 10?3 for C2H6, 2 × 10?4 for CH4, 1 × 10?3 for N2O, 1 × 10?4 for NO2, 4 × 10?5 for NH3, 1 × 10?3 for PH3, 7 × 10?4 for SO2, and 1 × 10?4 for OCS have been derived. 相似文献
10.
Michael B. McElroy 《Planetary and Space Science》1975,23(5):763-786
Models are presented for the height distribution of various photochemically active gases in Venus' upper atmosphere. Attention is directed to the chemistry and vertical transport of odd hydrogen (H, OH, HO2, H2O2), odd oxygen (O, O3), free chlorine (Cl, ClO, ClOO, Cl2), CO, O2, H2 and H2O. Supply of O2 may play a limiting role in the formation of a possible H2SO4 cloud on Venus. The supply rate is influenced by both chemical and dynamical processes in the stratosphere, and an analysis of recent spectroscopic data for O2 implies a lower limit to the appropriate eddy coefficient of about 3 × 105 cm2/sec. The abundances of thermospheric O and CO are determined largely by vertical mixing, and an analysis of Mariner 10 measurements of Venus' Lyman α airglow suggests that the eddy coefficient in the lower thermosphere may be as large as 5 × 107cm2sec. The corresponding values for the mixing ratios of O and CO at the ionospheric peak are approximately 1 per cent. The Lyman α data could be reconciled with larger values for thermospheric O, and smaller values for the vertical eddy coefficient, if non-thermal loss processes were to play a dominant role in hydrogen escape, and if the corresponding flux were to exceed 107 atoms/cm2/sec. A sink of this magnitude would imply major depletion of Venus' atmospheric water over geologic time, and would appear to require mixing ratios of H2O in the lower atmosphere in excess of 4 × 10?4. The extensive component to the Lyman α emission measured by Mariner 5 may be due to resonance scattering of sunlight by hot atoms formed by charge transfer with O+. The H scale height, therefore, may reflect the temperature of positive ions in Venus' topside ionosphere. 相似文献
11.
A radiative seasonal model which incorporates a multilayer radiative transfer treatment at wave-lengths longward of 7 μm is presented and applied to Saturn's stratosphere. Opacities due to H2-He, CH4, C2H2, and C2H6 are included. Season-dependent insolation is shown to produce a strong hemispheric asymmetry decreasing with depth at the Voyager encounter times, and seasonal amplitudes of 30°K at the poles are predicted in the high stratosphere. The ring-modulated dependence of the insolation and the orbital eccentricity are shown to have a significant effect. Calculations agree closely with the Voyager 1 and 2 radio occultation ingress profiles recorded at 76°S and 36.5°S for CH4/H2 = 3.5 + 1.4/? 1.0 × 10?3;the estimated errors include modeling systematic errors and uncertainties in the occultations profiles. The possible role of aerosols in the stratospheric heating is analyzed. The Voyager 2 egress profile recorded at 31°S cannot be reproduced by calculations. Some constraints on the C2H2 and C2H6 abundances are derived. The upper portion of the occultation profiles (p < 3mbar) can be matched for C2H2/H2 = 1.0 + 1.3/?0.6 × 10?7, C2H6/H2 = 1.5 + 1.8/?0.9 × 10?6 at 76°S and C2H2/H2 = 4 + 6/?4 × 10?8, C2H6/H2 = 6 + 9/?6 × 10?7 at 36.5°N. At the northern occultation latitude, the discrepancy with the concentrations derived from analysis of IRIS spectra by R. Courtin, D. Gautier, A. Marten, B. Bézard, and R. Hanel (1984, Astrophys. J.287) can be explained by a sharp variation of the mixing ratios of these gases with altitude in the upper stratosphere. Other interpretations are discussed. 相似文献
12.
The 8.6-μm emission feature of Titan's infrared spectrum was analyzed using the Voyager temperature-pressure profile. Although both C3H8 and CH3D have bands at that wavelength, we show that CH3D dominates the observed emission on Titan. We derived a CH3D/CH4 mixing ratio using this band and the strong CH4 band at 7.7 μm. The corresponding D/H ratio is 4.2?1.5+2 × 10?4, neglecting deuterium fractionation with other molecules. The main uncertainty in this value comes from the continuum emission characteristics. The D/H ratio is apparently significantly enhanced on Titan with respect to published values for Saturn. 相似文献
13.
The photochemistry of the stratosphere of Venus was modeled using an updated and expanded chemical scheme, combined with the results of recent observations and laboratory studies. We examined three models, with H2 mixing ratio equal to 2 × 10?5, 5 × 10?7, and 1 × 10?13, respectively. All models satisfactorily account for the observations of CO, O2, O2(1Δ), and SO2 in the stratosphere, but only the last one may be able to account for the diurnal behavior of mesospheric CO and the uv albedo. Oxygen, derived from CO2 photolysis, is primarily consumed by CO2 recombination and oxidation of SO2 to H2SO4. Photolysis of HCl in the upper stratosphere provides a major source of odd hydrogen and free chlorine radicals, essential for the catalytic oxidation of CO. Oxidation of SO2 by O occurs in the lower stratosphere. In the high-H2 model (model A) the OO bond is broken mainly by S + O2 and SO + HO2. In the low-H2 models additional reactions for breaking the OO bond must be invoked: NO + HO2 in model B and ClCO + O2 in model C. It is shown that lightning in the lower atmosphere could provide as much as 30 ppb of NOx in the stratosphere. Our modeling reveals a number of intriguing similarities, previously unsuspected, between the chemistry of the stratosphere of Venus and that of the Earth. Photochemistry may have played a major role in the evolution of the atmosphere. The current atmosphere, as described by our preferred model, is characterized by an extreme deficiency of hydrogen species, having probably lost the equivalent of 102–103 times the present hydrogen content. 相似文献
14.
The flux emitted by Titan's disk in millimeter lines of HCN, HC3N, CH3CN, and CO is calculated by means of a radiative transfer formulation which takes into account the sphericity of the atmosphere. It is demonstrated that the plane-parallel approximation for radiative transfer is no longer valid, especially in the core of emission lines, when Titan is not spatially resolved. The antenna temperatures which would be measured by large radiotelescopes observing Titan at frequencies of (1?0) and (2?1) transitions of CO, of (1?0), (2?1), and (3?2) transitions of HCN, and of selected transitions of HC3N and CH3CN in the range 80–300 GHz are calculated. The observability of these transitions is investigated. It is concluded that there is the possibility of inferring the vertical stratospheric distribution of these species from line shape measurements to be achieved with existing or forthcoming radioastronomical instrumentation. The determination of the CO abundance by D. O. Muhleman, G. L. Berge, and R. T. Clancy (1984, (Science (Washington, D.C.), 223, 393–396) from measurements at 115.3 GHz in two 200 MHz bands, is reinterpreted by means of this radiative transfer formulation. A CO mixing ratio between 3 × 10?5 and 18 × 10?5, with a most plausible value of 7.5 × 10?5, is found. 相似文献
15.
A review is given of the stratospheric budgets of odd oxygen, odd nitrogen, nitrous oxide, methane and carbonyl sulfide. The stratospheric column production rate of NO by the reaction N2O + O(1D) → 2 NO is 1.1–1.9 × 108 molecules cm?2 s?1. The stratospheric loss rates for N2O, CH4 and COS are equal to 0.9–1.4 × 109, 1 × 1010 and 0.5 × 107 molecules cm?2 s?1, respectively. From currently available information on the global distributions of N2O and CH4 there are some indications of about two times smaller OH concentrations below 35 km than those which are calculated based on the latest compilation of kinetic data.Most significantly, however, it is shown that photochemical models and available ozone observations cannot be reconciled and that there may be particularly severe problems in the 25–35 km region. This issue is thoroughly discussed.Volcanic emissions of SO2 to the stratosphere may locally lead to much enhanced ozone concentrations and heating rates. These may influence the dynamic behaviour of volcanic plumes before their dispersion over large volumes of the stratosphere. 相似文献
16.
The Q and R branches of the C2H2 ν5 fundamental, observed in emission in an aircraft spectrum of Jupiter near 750 cm?1, have been analyzed with the help of an improved line listing for this band. The line parameters have been certified in the laboratory with the same interferometer used in the Jovian observations. The maximum mixing ratio of C2H2 is found to be between 5 × 10?8 and 6 × 10?9, depending on the form of its vertical distribution and the temperature structure assumed for the lower stratosphere. Most consistent with observations of both Q and R branches are: (1) distributions of C2H2 with a constant mixing ratio in the stratosphere and a cutoff at a total pressure of 100 mbar or less, and (2) the assumption of a temperature at 10?2 bar which is near 155°K. 相似文献
17.
Results of the scattered solar radiation spectrum measurements made deep in the Venus atmosphere by the Venera 11 and 12 descent probes are presented. The instrument had two channels: spectrometric (to measure downward radiation in the range 0.45 < γ < 1.17 μm) and photometric (four filters and circular angle scanning in an almost vertical plane). Spectra and angular scans were made in the height range from 63 km above the planet surface. The integral flux of solar radiation is 90 ± 12 W m?2 measured on the surface at the subsolar point. The mean value of surface absorbed radiation flux per planetary unit area is 17.5 ± 2.3 W m?2. For Venera 11 and 12 landing sites the atmospheric absorbed radiation flux is ～15 W m?2 for H >; 43 km and ～45 W m?2 for H < 48 km in the range 0.45 to 1.55 μm. At the landing sites of the two probes the investigated portion of the cloud layer has almost the same structure: it consists of three parts with boundaries between them at about 51 and 57 km. The base of clouds is near 48 km above the surface. The optical depth of the cloud layer (below 63 km) in the range 0.5 to 1 μm does not depend on the wavelength and is ～29 and ～38 for the Venera 11 and 12 landing sites, respectively. The single-scattering albedo, ω0, in the clouds is very close to 1 outside the absorption bands. Below 58 km the parameter (1 ? ω0) is <10?3 for 0.49 and 0.7 μm. The parameter (1 ? ω0) obviously increases above 60 km. Below 48 km some aerosol is present. The optical depth here is a strong function of wavelength. It varies from 1.5 to 3 at λ = 0.49 μm and from 0.13 to 0.4 at 1.0 μm. The mean size of particles below the cloud deck is about 0.1 μm. Below 35 km true absorption was found at λ < 0.55 μm with the (1 ? ω0) maximum at H ≈ 15 km. The wavelength and height dependence of the absorption coefficient are compatible with the assumption that sulfur with a mixing ratio ～2 × 10?8 normalized to S2 molecules is the absorber. The upper limits of the mixing ratio for Cl2, Br2, and NO2 are 4 × 10?8, 2 × 10?11, and 4 × 10?10, respectively. The CO2 and H2O bands are confidently identified in the observed spectra. The mean value of the H2O mixing ratio is 3 × 10?5 < FH2O < 10?4 in the undercloud atmosphere. The H2O mixing ratio evidently varies with height. The most probable profile is characterized by a gradual increase from FH2O = 2 × 10?5 near the surface to a 10 to 20 times higher value in the clouds. 相似文献
18.
Models are developed to describe the photochemistry of ozone on Mars. Catalytic reactions involving H, OH and HO2 play a major role at low latitudes where they ensure a vertical column density for O3 of less than 2 × 10?4 cm atm. The source for odd hydrogen (H + OH + HO2) is relatively smaller at high latitudes in winter due to the small concentrations of H2O present there at that time. Odd hydrogen is also efficiently removed from the high-latitude winter atmosphere by condensation of H2O2. The role of catalytic chemistry is reduced accordingly and the vertical column density of O3 may be as large as 5.7 × 10?3 cm atm in accord with earlier observations carried out by Barth and co-workers with instruments on Mariner 9. 相似文献
19.
V.G. Teifel 《Icarus》1983,53(3):389-398
Modeling of the geometric albedo of Uranus in and near prominent methane absorption bands between 0.5 and 0.9 μm indicates that the visible atmosphere probably consists of a thin aerosol haze layer (τscat ? 0.3?0.5; ωH ? 0.95) above an optically thick, semi-infinite Rayleigh scattering atmosphere. A significant depletion of methane gas above the haze layer is indicated. The mixing ratio of methane in the lower atmosphere is consistent with a value of CH4/H2 ? 3 × 10?3, comparable to those derived for Jupiter and Saturn. 相似文献
20.
A spectroscopic search for H2O and CH4 in Comet Kohoutek (1973f) was made using a Pepsios interferometer. No evidence was found for either molecule, allowing us to set an upper limit on their production rates (on about 21 January 1974) of Q(H2O) < 6.2 × 1028 sec?1 and Q(CH4) < 2.0 × 1030 sec?1. If the cometary surface is water-ice, this production rate leads to a product (1 ? A)·(πR02) < 2.2 km2, where A is the Bond albedo, R0 is the nuclear radius, and we assume that all the absorbed solar energy is used to evaporate H2O. 相似文献