The abundance of acetylene in the atmosphere of Jupiter

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.     

A determination of the composition of the Saturnian stratosphere using the IUE

We reduced ultraviolet spectra of Saturn from the IUE satellite to produce a geometric albedo of the planet from 1500 to 3000 Å. By matching computer models to the albedo we determined a chemical composition consistent with the data. This model includes C₂H₂ and C₂H₆ with mixing ratios and distributions of (9 ± 3) × 10^?8 in the top 20 mbar of the atmosphere with none below for C₂H₂ and (6 ± 1) × 10^?6 also in the top 20 mbar with none below for C₂H₆. The C₂H₂ and C₂H₆ distributions and the C₂H₆ mixing ratio are taken directly from the Voyager IRIS model [R. Courtin et al., Bull. Amer. Astron. Soc.13, 722 (1981), and private communication]. The Voyager IRIS model also includes PH₃, which is not consistent with the uv albedo from 1800 to 2400 Å. Our model requires a previously unidentified absorber to explain the albedo near 1600 Å. After considering several candidates, we find that the best fit to the data is obtained with H₂O, having a column density of (6 ± 1) × 10^?3 cm-am.     

An estimate of the PH3, CH3D,and GeH4 Abundances on Jupiter from the Voyager IRIS data at 4.5 μm

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.     

Mixing ratios of methane,ethane, and acetylene in Neptune's stratosphere

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.     

Postperihelion interference filter photometry of the “annual” comet P/Encke

Interference filter photometry was taken of Comet Encke on June 14, 1974 (1.07 AU heliocentric distance, postperihelion) at the CTIO (Cerro Tololo Interamerican Observatory) 150-cm reflector. Production rates were calculated of 4.1 × 10²³ mol sec^?1 of CN, 5.3 × 10²³ mol sec^?1 of C₃, and 4.3 × 10²⁴ mol sec^?1 of C₂. These are about three times smaller than at comparable heliocentric distance preperihelion, assuming a value of 100 for the ratio H₂O/ (C₂ + C₃ + CN). An upper limit was placed on the production of nonvolatiles at about one-third that of volatiles in mass by assuming a bulk density of 1 g cm^?3, a particle geometric albedo of 0.1, and a phase function of 0.2.     

Photochemistry of the stratosphere of Venus: Implications for atmospheric evolution

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 OO bond is broken mainly by S + O₂ and SO + HO₂. In the low-H₂ models additional reactions for breaking the OO 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 NO_x 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.     

Variations of the stratospheric temperature along the limb of Uranus: Results of the 22 April 1982 stellar occultation

Stratospheric temperature profiles of Uranus were derived from the stellar occultation of 22 April 1982 in the pressure range 5–30 μbar. The observations were made at the European Southern Observatory, Chile, and at the Observatoire du Pic du Midi et de Toulouse, France with two telescopes in both sites. The study of these profiles confirms that Uranus' stratosphere is warmer than had been expected from radiative models (J. F. Appleby, 1980, Atmospheric Structures of the Giant Planets from Radiative-Convective Equilibrium Models. PhD. Thesis, State University of New York at Stony Brook) and that there has been a general increase of temperature since 1977 (R. G. French, J. L. Elliot, E. W. Dunham, D. A. Allen, J. H. Elias, J. A. Frogel, and W. Liller, 1983, Icarus53, 399–414). Furthermore, the profiles exhibit a nonisothermal feature with a maximum temperature around the 8-μbar pressure level. The amplitude of this feature increases linearly with the diurnally averaged insolation 〈D〉 up to the observed value 〈D〉 ～ 0.15. Moreover, the temperature at 8 μbar, as well as the mean stratospheric temperature, reaches a plateau around the equator of the planet which is far from maximum insolation. For a nominal abundance of methane η_CH4 ～ 3 × 10^?5 and normal incidence, the UV absorption could compete with the IR methane absorption bands at the pressure level 8 μbar. However, the high temperatures observed even at grazing incidence imply important circulation phenomena to isothermalize distant regions of the planet. Alternatively, the observed profiles may suggest that an optically thin aerosol layer distributed over one scale height is responsible for the temperature maximum at 8 μbar. The total mass of dust necessary to heat this region up significantly would be a small fraction (6 × 10¹⁰ g vs 5 × 10¹⁸ g) of the Uranian ring system, which appears then as a possible reservoir of dust. However, a falling rate of ～1 msec^?1 would deplete the rings in a short time (≈2 × 10⁵ years) so that a dynamical process is needed to sustain the aerosol layer.     

On the production of nitric oxide by cosmic rays in the mesosphere and stratosphere

Nitric oxide is formed in the atmosphere through the ionization and dissociation of molecular nitrogen by galactic cosmic rays. One NO molecule is formed for each ion pair produced by cosmic ray ionization.The height-integrated input (day and night) to the lower stratosphere is of the order of 6 × 10⁷ NO molecules cm^?2/sec in the auroral zone (geomagnetic latitude Φ ? 60°) during the minimum of the sunspot cycle and 4 × 10⁷ NO molecules cm^?2/sec in the subauroral belt and auroral region (Φ? 45°) at the maximum of solar activity. The tropical production is less than 10^?7 NO molecules cm^?2/sec above 17 km and at the equator the production is only 3 × 10⁶NO molecules cm^?2/sec.     

Phosphine photochemistry in the atmosphere of Saturn

A model is presented for the photochemistry of PH₃ in the upper troposphere and lower stratosphere of Saturn that includes the effects of coupling with NH₃ and hydrocarbon photochemistry, specifically the C₂H₂ catalyzed photodissociation of CH₄. PH₃ is rapidly depleted with altitude (scale height ～35 km) in the upper troposphere when K～10⁴cm²sec^?1; an upper limit for K at the tropopause is estimated at ～10⁵cm²sec^?1. If there is no gas phase P₂H₄ because of sublimation, P₂ and P₄ formation is unlikely unless the rate of the spin-forbidden recombination reaction PH + H₂ + M → PH₃ + M is exceedingly slow. An upper limit P₄ column density of ～2×10¹⁵cm^?2 is estimated in the limit of no recombination. If sublimation does not remove all gas phase P₂H₄, P₂ and P₄ may be produced in potentially larger quantities, although they would be restricted almost entirely to the lowest levels of our model, where T?100°K. Potentially observable amounts of the organophosphorus compounds CH₃P₂H₂ and HCP are predicted, with column densities of >10¹⁷ cm^?2 and production rates of ～2×10⁸cm^?2sec^?1. The possible importance of electronically excited states of PH_x and additional PH₃/hydrocarbon photochemical coupling paths are also considered.     

The abundance of water on Jupiter from the voyager IRIS data at 5 μm

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 $\text{H}{}_2\text{O}\text{H}{}_2\text{=(4.0±1.0) × 10}{}^{\mathrm{?6}}$, 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.     

Simultaneous measurements of No and No2 in the stratosphere

Simultaneous measurements of NO and NO₂ in the stratosphere leading to an NO_x determination have been performed by means of i.r. absorption spectrometry using the Sun as a source in the 5·2 μm band of NO and in the 6·2 μm band of NO₂. The observed abundance of NO_P peaks at 26 km where it is equal to (4·2 ± 1) × 10⁹ cm^?3. The volume mixing ratio of NO_p was observed to vary from 1·3 × 10^?9 at 20 km to 1·3 × 10^?8 at 34 km.     

Titan: Far-infrared and microwave remote sensing of methane clouds and organic haze

It is shown that Titan's surface and plausible atmospheric thermal opacity sources—gaseous N₂, CH₄, and H₂, CH₄ cloud, and organic haze—are sufficient to match available Earth-based and Voyager observations of Titan's thermal emission spectrum. Dominant sources of thermal emission are the surface for wavelenghts λ ? 1 cm, atmospheric N₂ for 1 cm ? λ ? 200 μm,, condensed and gaseous CH₄ for 200 μm ? λ ? 20 μm, and molecular bands and organic haze for λ ? 20 μm. Matching computed spectra to the observed Voyager IRIS spectra at 7.3 and 52.7° emission angles yields the following abundances and locations of opacity sources: CH₄ clouds: 0.1 g cm^? at a planetocentric radius of 2610–2625 km, 0.3 g cm^?2 at 2590–2610 km, total 0.4 ± 0.1 g cm^–2 above 2590 km; organic haze: $\text{4 ± 2 × 10}{}^{\mathrm{?6}}\text{,}\text{g cm}\text{,}{}^{\mathrm{?2}}$ above 2750 km; tropospheric H₂: 0.3 ± 0.1 mol%. This is the first quantitative estimate of the column density of condensed methane (or CH₄/C₂H₆) on Titan. Maximum transparency in the middle to far IR occurs at 19 μm where the atmospheric vertical absorption optical depth is $\text{?0.6}$ A particle radius $\text{r}\text{? 2 μ}\text{m}$ in the upper portion of the CH₄ cloud is indicated by the apparent absence of scattering effects.     

Equatorial ozone profiles from the solar maximum mission—a comparison with theory

The u.v. spectrometer polarimeter on the Solar Maximum Mission has been utilized to measure mesospheric ozone vs altitude profiles by the technique of solar occultation. Sunset data are presented for 1980, during the fall equinoctal period within ± 20° of the geographic equator. Mean O₃, concentrations are 4.0 × 10¹⁰ cm^?3at 50 km, 1.6 × 10¹⁰ cm^?3 at 55 km. 5.5 × 10⁹ cm^?3 at 60 km and 1.5 × 10⁹ cm^?3 at 65 km. Som profiles exhibit altitude structure which is wavelike. The mean ozone profile is fit best with the results of a time-dependent model if the assumed water vapor mixing ratio employed varies from 6 ppm at 50 km to 2–4 ppm at 65 km.     

On the structure of Mars' atmosphere at 120–220 km

Altitude dependences of [CO₂] and [CO₂⁺] are deduced from Mariner 6 and 7 CO₂⁺ airglow measurements. CO₂ densities are also obtained from n_e radio occultation measurements. Both [CO₂] profiles are similar and correspond to the model atmosphere of Barth et al. (1972) at 120 km, but at higher altitudes they diverge and at 200–220 km the obtained [CO₂] values are three times less the model. Both the airglow and radio occultation observations show that a correction factor of 2.5 should be included into the values for solar ionization flux given by Hinteregger (1970). The ratio of [CO₂⁺]/n_e is 0.15–0.2 and, hence, [O]/[CO₂] is ～3% at 135 km. An atmospheric and ionospheric model is developed for 120–220 km. The calculated temperature profile is characterized by a value of T ≈ 370°K at h ? 220 km, a steep gradient (～2°/km) at 200-160 km, a bend in the profile at 160 km, a small gradient (～0.7°/km) below and a value of T ≈ 250°K at 120 km. The upper point agrees well with the results of the Lyman-α measurements; the steep gradient may be explained by molecular viscosity dissipation of gravity and acoustical waves (the corresponding energy flux is 4 × 10^?2 erg cm^?2sec^?1 at 180 km). The bend at 160 km may be caused by a sharp decrease of the eddy diffusion coefficient and defines K ≈ 2 × 10⁸cm²sec^?1; and the low gradient gives an estimate of the efficiency of the atmosphere heating by the solar radiation as ? ≈ 0.1.     

Titan’s atmosphere from ISO mid-infrared spectroscopy

We have analyzed Titan observations performed by the Infrared Space Observatory (ISO) in the range 7-30 μm. The spectra obtained by three of the instruments on board the mission (the short wavelength spectrometer, the photometer, and the camera) were combined to provide new and more precise thermal and compositional knowledge of Titan’s stratosphere. With the high spectral resolution achieved by the SWS (much higher than that of the Voyager 1 IRIS spectrometer), we were able to detect and separate the contributions of most of the atmospheric gases present on Titan and to determine disk-averaged mole fractions. We have also tested existing vertical distributions for C₂H₂, HCN, C₂H₆, and CO₂ and inferred some information on the abundance of the first species as a function of altitude. From the CH₃D band at 1161 cm⁻¹ and for a CH₄ mole fraction assumed to be 1.9% in Titan’s stratosphere, we have obtained the monodeuterated methane-averaged abundance and retrieved a D/H isotopic ratio of 8.7−1.9+3.2 × 10⁻⁵. We discuss the implications of this value with respect to current evolutionary scenarios for Titan. The ν₅ band of HC₃N at 663 cm⁻¹ was observed for the first time in a disk-averaged spectrum. We have also obtained a first tentative detection of benzene at 674 cm⁻¹, where the fit of the ISO/SWS spectrum at R = 1980 is significantly improved when a constant mean mole fraction of 4 × 10⁻¹⁰ of C₆H₆ is incorporated into the atmospheric model. This corresponds to a column density of ∼ 2 × 10¹⁵ molecules cm⁻² above the 30-mbar level. We have also tested available vertical profiles for HC₃N and C₆H₆ and adjusted them to fit the data. Finally, we have inferred upper limits of a few 10⁻¹⁰ for a number of molecules proposed as likely candidates on Titan (such as allene, acetonitrile, propionitrile, and other more complex gases).     

Gravity field of Mars from Mariner 9 tracking data

Further reduction of Doppler tracking data from Mariner 9 confirms our earlier conclusion that the gravity field of Mars is considerably rougher than the fields of either the Earth or the Moon. The largest positive gravity anomaly uncovered is in the Tharsis region which is also topographically high and geologically unusual. The best determined coefficients of the harmonic expansion of the gravitational potential are: J₂ = (1.96 ± 10.01) × 10^?3 ; C₂₂ = ?(5.1 ± 0.2) × 10^?5; and S₂₂ = (3.4 ± 0.2) × 10^?5. The other coefficients have not been well determined on an individual basis, but the ensemble yields a useful model for the gravity field for all longitudes in the vicinity of 23° South latitude which corresponds to the periapse position for the orbiter.The value obtained for the inverse mass of Mars (3 098 720 ± 70 M⊙^?1) is in good agreement with prior determinations from Mariner flyby trajectories. The direction found for the rotational pole of Mars, referred to the mean equinox and equator of 1950.0, is characterized by α = 317°.3 ± 0°.2, δ = 52°.7 ± 0°.2. This result is in excellent agreement with Sinclair's recent value, determined from earth-based observations of Mars' satellites, but differs by about 0°.5 from the previously accepted value. Other important physical constants that have either been refined or confirmed by the Mariner 9 data include: (i) the dynamical flattening, f = (5.24 ± 0.02) × 10^?3; (ii) the maximum principal moment of inertia, C = (0.375 ± 0.006) MR²; and (iii) the period of precession of Mars' pole, P ? (1.73 ± 0.03) × 10⁵ yr, corresponding to a rate of 7.4 sec of arc per yr.     

Measurements of positive ion conversion and removal reactions relating to the Jovian ionosphere

Measured rates are presented for the reaction of He⁺ ions with H₂ (and D₂) molecules to form H⁺, H₂⁺, and HeH⁺ ions, as well as for the subsequent reactions of H⁺ and HeH⁺ ions with H₂ to form H₃⁺. The neutralization of H₃⁺ (and H₅⁺) ions by dissociative recombination with electrons is shown to be fast. The reaction He⁺ + H₂ is slow (k = 1.1 × 10^?13 cm³/sec at300°K) and produces principally H⁺ by the dissociative charge transfer branch. It is concluded that there may be a serious bottleneck in the conversion of two of the primary ions of the upper Jovian ionosphere, H⁺ and He⁺ (which recombine slowly), to the rapidly recombining H₃⁺ ion (α[H₃⁺]?3.4 × 10^?7 cm³/sec at 150°K).     

Production and condensation of organic gases in the atmosphere of Titan

The rates and altitudes for the dissociation of atmospheric constituents of Titan are calculated for solar UV, solar wind protons, interplanetary electrons, Saturn magnetospheric particles, and cosmic rays. The resulting integrated synthesis rates of organic products range from 10²–10³ g cm^?2 over 4.5 × 10⁹ years for high-energy particle sources to 1.3 × 10⁴ g cm^?2 for UV at $\text{λ < 1550}\text{A}\text{?}$, and to 5.0 × 10⁵ g cm^?2 if $\text{λ > 1550}\text{A}\text{?}$ (acting primarily on C₂H₂, C₂H₄, and C₄H₂) is included. The production rate curves show no localized maxima corresponding to observed altitudes of Titan's hazes and clouds. For simple to moderately complex organic gases in the Titanian atmosphere, condensation occurs below the top of the main cloud deck at 2825 km. Such condensates comprise the principal cloud mass, with molecules of greater complexity condensing at higher altitudes. The scattering optical depths of the condensates of molecules produced in the Titanian mesosphere are as great as ～ 10²/(particulate radius, μm) if column densities of condensed and gas phases are comparable. Visible condensation hazes of more complex organic compounds may occur at altitudes up to ～ 3060 km provided only that the abundance of organic products declines with molecular mass no faster than laboratory experiments indicate. Typical organics condensing at 2900 km have molecular masses = 100–150 Da. At current rates of production the integrated depth of precipitated organic liquids, ices, and tholins produced over 4.5 × 10⁹ years ranges from a minimum ～ 100 m to kilometers if UV at $\text{λ > 1550}\text{A}\text{?}$ is important. The organic nitrogen content of this layer is expected to be ～ 10^?1?10^?3 by mass.     

Laboratory measurements of the microwave opacity and vapor pressure of sulfuric acid vapor under simulated conditions for the middle atmosphere of Venus

Microwave absorption observed in the 35- to 48-km-altitude region of the Venus atmosphere has been attributed to the presence of gaseous sulfuric acid (H₂SO₄) in that region. This has motivated the laboratory measurement of the microwave absorption at 13.4- and 3.6-cm wavelengths from gaseous H₂SO₄ in a CO₂ atmosphere under simulated conditions for that region. As part of the same experiments, upper limits on the saturation vapor pressure of gaseous H₂SO₄ have also been determined. The measurements for microwave absorption have been made in the 1- to 6-atm pressure range, with temperatures in the 500 to 575°K range. Using a theoretically derived temperature dependence, the best-fit expression for absorption from gaseous H₂SO₄ in a CO₂ atmosphere at the 13.4-cm wavelength is $\text{9.0 × 10}{}^9\text{q(P)}{}^{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{T}{}^{\mathrm{?3}}\text{(}\text{dB km}{}^{\mathrm{?1}}\text{),}\text{where}\text{q}$ is the H₂SO₄ number mixing ratio, P is the pressure in atmospheres, and T is the temperature in degrees Kelvins. The best-fit expression for absorption at the 3.6-cm wavelength is 4.52 × 10¹⁰q(P)^0.85T^?3 (dB km^?1). The inferred H₂SO₄ vapor pressure above liquid H₂SO₄ corresponds to ln p = 8.84 ? 7220/t where p is the H₂SO₄ vapor pressure (in atm) and T is the temperature in degrees Kelvins. These results suggest that abundances of gaseous H₂SO₄ on the order of 15 to 30 ppm could account for the microwave absorption observed by radio occultation experiments at 13.3- and 3.6-cm wavelengths. They also suggest that such abundances would correspond to saturation vapor pressure existing at or above the 46- to 48-km range, which correlates with the observed cloud base. It is suggested that future measurements of absorption in the 1- to 3-cm wavelength range will provide additional tools for monitoring variations in H₂SO₄ abundance via radio occultation and radio astronomical observations.     

Galilean satellite eclipse studies: III. Jovian methane abundance

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.