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Chemical abundances in cold, dark interstellar clouds.

The Sun may well have formed in the type of interstellar cloud currently referred to as a cold, dark cloud. We present current tabulations of the totality of known interstellar molecules and of the subset which have been identified in cold clouds. Molecular abundances are given for two such clouds which show interesting chemical differences in spite of strong physical similarities, Taurus Molecular Cloud 1 (TMC-1) and Lynd's 134N (L134N, also referred to as L183). These regions may be at different evolutionary stages.

Acetonitriles↗

Laboratory studies of the newly discovered infrared band at 4705.2 cm-1 (2.1253 micrometers) in the spectrum of Io: the tentative identification of CO2.

We discuss over 120 laboratory experiments pertaining to the identification of the new absorption band discovered by Trafton et al. (1991) at 4705.2 cm-1 (2.1253 micrometers) in the spectrum of Io. It is shown that this band is not due to overtones or combinations of the fundamental bands associated with the molecules (or their chemical complexes) already identified on Io, namely, SO2, H2S, and H2O. Thus, this band is due to a new, previously unidentified, component of Io. Experiments also demonstrate that the band is not due to molecular H2 frozen in SO2 frosts. Since the frequency of this band is very close to the first overtone of the nu 3 asymmetric stretching mode of CO2, we have investigated the spectral behavior of CO2 under a variety of conditions appropriate for Io. The profile of the Io band is not consistent with the rotational envelope expected for single, freely rotating, gaseous CO2 under Io-like conditions. It was found that pure, solid CO2 and CO2 intimately mixed in a matrix of solid SO2 and H2S produce bands with similar widths (5-10 cm-1), but that these bands consistently fall at frequencies about 10-20 cm-1 (approximately 0.007 micrometer) lower than the Io band. CO2 in SO2 : H2S ices also produces several additional bands that are not in the Io spectra. The spectral fit improves, however, as the CO2 concentration in SO2 increases, suggesting that CO2-CO2 interactions might be involved. A series of Ar : CO2 and Kr : CO2 matrix isolation experiments, as well as laboratory work done elsewhere, show that CO2 clustering shifts the band position to higher frequencies and provides a better fit to the Io band. Various laboratory experiments have shown that gaseous CO2 molecules have a propensity to cluster between 80 and 100 K, temperatures similar to those found on the colder regions of Io. We thus tentatively identify the newly discovered Io band at 4705.2 cm-1 (2.1253 micrometers) with CO2 multimers or "clusters" on Io. Whether these clusters are buried within an SO2 frost, reside on the surface, or are in a residual, steady-state "atmospheric aerosol" population over local coldtraps is not entirely clear, although we presently favor the latter possibility. The size of these clusters is not well defined, but evidence suggests groups of more than four molecules are required. The absorption strength of the 2 nu 3 CO2 cluster overtone determined in the laboratory, in conjunction with the observed strength of the Io band, suggests that the disk-integrated abundance of CO2 is less than 1% that of the SO2. Studies of the sublimation behavior of CO2 indicate that it probably resides predominantly in the cooler areas (< 100 K) of Io. The relative constancy of the Io feature over a variety of orbital phases suggests that the polar regions may contain much of the material. Some consequences of the physical properties of CO2 under conditions pertinent to Io are discussed. The presence of CO2 clusters on Io could be verified by the detection of any one of several other infrared bands associated with the CO2 molecule, of which the strongest are the nu 3 12CO2 asymmetric stretch fundamental near 2350 cm-1 (4.25 micrometers) and the nu 2 bending mode fundamental near 660 cm-1 (15.1 micrometers). Weaker bands that may also be detectable include the nu 3 13CO2 asymmetric stretch fundamental near 2280 cm-1 (4.39 micrometers), the 2 nu 2 + nu 3 combination/overtone band near 3600 cm-1 (2.78 micrometers), and the nu 1 + nu 3 combination band near 3705 cm-1 (2.70 micrometers).

Astronomical Phenomena↗

CO2 condensation and the climate of early Mars.

A one-dimensional, radiative-convective climate model was used to reexamine the question of whether early Mars could have been kept warm by the greenhouse effect of a dense, CO2 atmosphere. The new model differs from previous models by considering the influence of CO2 clouds on the convective lapse rate and on the the planetary radiation budget. Condensation of CO2 decreases the lapse rate and, hence, reduces the magnitude of the greenhouse effect. This phenomenon becomes increasingly important at low solar luminosities and may preclude warm (0 degree C), globally averaged surface temperatures prior to approximately 2 billion years ago unless other greenhouse gases were present in addition to CO2 and H2O. Alternative mechanisms for warming early Mars and explaining channel formation are discussed.

Atmosphere↗

A new class of absorption feature in Io's near-infrared spectrum.

We report our discovery of an absorption feature in the infrared spectrum of Io centered at 2.1253 micrometers (4705.2 cm-1). This band is marginally resolved at resolving power 1200 with a deconvolved full width at half-maximum (FWHM) of about 4 cm-1. This contrasts with the 30- to 50-cm-1 widths of the broad absorption features previously detected at longer wavelengths which arise from mixtures of SO2 with H2S and H2O. This newly discovered feature is relatively weak, having a core only 5% below the continuum at this resolving power. Our survey from 1.98 to 2.46 micrometers (5050-4065 cm-1) at this same resolving power revealed no other feature greater than 1% of the continuum level shortward of 2.35 micrometers, and 3% elsewhere. The feature does not correspond to any gas- or solid-phase absorption that might be expected from previously identified constituents of Io's surface. No temporal or longitudinal variation has been detected in the course of 18 nights of observation over the past year and no significant variation in the strength of the feature was seen during an emergence from eclipse. These observations indicate that the source material of the feature is reasonably stable, and is more uniformly distributed in longitude than Io's hot spots. These characteristics all indicate that the feature belongs to a class different from those characterizing other known absorption features in Io's spectrum. Consequently, it should reveal important new information about Io's atmosphere-surface composition and interaction. A series of laboratory experiments of plausible surface ices indicates that (i) the band does not arise from overtones or combinations of any of the molecular vibrations associated with species already identified on Io (SO2, H2S, H2O) or from chemical complexes of these molecules, (ii) the band does not arise from H2 trapped in SO2, and (iii) the band may arise from the 2 nu3 mode of CO2. If the band arises from CO2, it is clear from its detailed shape and position that the molecules are not embedded in an SO2 matrix, as are H2S and H2O, but may be present as multimers or "clusters."

Atmosphere↗

Troposphere-stratosphere interactions in a one-dimensional model of Jovian photochemistry.

A simple one-dimensional model of the Jovian atmosphere including the coupling between a rapidly mixed troposphere and a stagnant stratosphere is presented. We treat analytically the case of a chemically unreactive species flowing downward through the stratosphere and troposphere with a constant flux. The calculated concentration profile has a maximum value approximately one atmospheric scale height above the tropopause. The corresponding mixing ratio rapidly decreases in the lower stratosphere. The contrast between the peak stratosphere and tropopause concentrations reflects the variation between the lower stratosphere and upper troposphere eddy diffusion coefficients. Numerical simulations of unreactive CO and C2H6, considering high-altitude photochemical sources (yielding downward fluxes to the troposphere) and deep troposphere thermochemical sources, demonstrate that upper troposphere abundances may have a large photochemical contribution. Recent observations of CO near 5 bar can be reproduced by a model using any one of three different tropospheric eddy diffusion profiles: a constant value of approximately 10(8) cm2 sec-1, a constant value of < or approximately 10(4) cm2 sec-1, or a two-layer model with a rapidly mixed (10(8) cm2 sec-1) layer below 20 bar and a slower mixing layer (10(4) cm2 sec-1) between 100 mbar and 20 bar. In the latter two scenarios, the photochemical source is an important and/or dominant source of upper tropospheric CO. However, the upper tropospheric C2H6 abundances are distinctly different among the three cases. These calculations suggest objectives for higher spectral resolution observations, critical vertical scales for planning experiments on future missions to Jupiter, and predictions that can be tested with the Galileo probe mass spectrometer.

Atmosphere↗

Titan's surface and troposphere, investigated with ground-based, near-infrared observations.

New observations of Titan's near-infrared spectrum (4000-5000 cm-1) combined with points taken from Fink and Larson's (1979) spectrum (4000-12500 cm-1) provide information on Titan's haze, possible clouds, surface albedo, and atmospheric abundance of H2. In the near-infrared, the main features in Titan's spectrum result from absorption of solar radiation by CH4. The strength of this absorption varies considerably with wavelength, allowing us to probe various atmospheric levels down to the surface itself by choosing specific wavelengths for analysis. At 4715 cm-1, the pressure-induced S(1) fundamental band of H2 lies in the wings of CH4 bands. Based on current values for the CH4 line parameters, Titan's spectrum can be best interpreted with a volume mixing ratio of H2 between 0.5 and 1.0%. Our observations suggest the existence of an optically thin CH4 cloud layer. The optical depths that we derive for Titan's haze and clouds are small enough to allow us to sense the surface of Titan at 4900, 6250, and 7700 cm-1. The most plausible interpretation of the albedos determined at these wavenumbers suggests a surface dominated by "dirty" water ice. A global ethane ocean is not compatible with these albedos.

Atmosphere↗

CH4/NH3/H2O spark tholin: chemical analysis and interaction with Jovian aqueous clouds.

The organic solid (tholin) produced by spark discharge in a CH4 + NH3 + H2O atmosphere is investigated, along with the separable components of its water-soluble fraction. The chemistry of this material serves as a provisional model for the interaction of Jovian organic heteropolymers with the deep aqueous clouds of Jupiter. Intact (unhydrolyzed) tholin is resolved into four chemically distinct fractions by high-pressure liquid chromatography (HPLC). Gel filtration chromatography reveals abundant components at molecular weights approximately or equal to 600-700 and 200-300 Da. Gas chromatography/mass spectrometry of derivatized hydrolysis products of unfractionated tholin shows about 10% by mass protein and nonprotein amino acids, chiefly glycine, alanine, aspartic acid, beta-alanine, and beta-aminobutyric acid, and 12% by mass other organic acids and hydroxy acids. The stereospecificity of alanine is investigated and shown to be racemic. The four principal HPLC fractions yield distinctly different proportions of amino acids. Chemical tests show that small peptides or organic molecules containing multiple amino acid precursors are a possibility in the intact tholins, but substantial quantities of large peptides are not indicated. Candidate 700-Da molecules have a central unsaturated, hydrocarbon- and nitrile-rich core, linked by acid-labile (ester or amide) bonds to amino acid and carboxylic acid side groups. The core is probably not HCN "polymer." The concentration of amino acids from tholin hydrolysis in the lower aqueous clouds of Jupiter, about 0.1 micromole, is enough to maintain small populations of terrestrial microorganisms even if the amino acids must serve as the sole carbon source.

Amino Acids↗

On the possibility of chemosynthetic ecosystems in subsurface habitats on Mars.

We have reexamined the question of extant microbial life on Mars in light of the most recent information about the planet and recently discovered nonphotosynthetic microbial ecosystems on Earth--deep sea hydrothermal vent communities and deep subsurface aquifer communities. On Mars, protected subsurface niches associated with hydrothermal activity could have continued to support life even after surface conditions became inhospitable. Geochemical evidence from the SNC meteorites and geomorphological evidence for recent volcanism suggest that such habitats could persist to the present time. There are also extensive geological features that attest to the ubiquitous nature of volcano-ground ice interactions on Mars. We suggest a possible deep subsurface microbial ecology similar to those discovered to depths of several kilometers below the surface of the Earth. We focus on anaerobic systems utilizing CO2 as the primary source of carbon. Liquid water could be provided by the heat of geothermal or volcanic activity melting permafrost or other subsurface water sources. Gases from volcanic activity deep in the planet could provide reducing power (as CH4, H2, or H2S) percolating up from below and enabling the development of a microbial community based upon chemolithoautotrophy. We suggest a methanogen (or acetogen) and sulfur-based microbial ecology as one possible basis for microbial primary production. Our hypothetical ecosystem is neither supported, nor excluded, by current observations of Mars. Tests for such a subsurface system involve locating active geothermal areas associated with ground ice or detecting trace quantities of reduced atmospheric gases that would leak from such a system.

Carbon Dioxide↗

Minor constituents in the Martian atmosphere from the ISM/Phobos experiment.

Global Martian atmospheric results derived from the infrared imaging spectrometer ISM flown aboard the Phobos 2 Soviet spacecraft are presented. Over low altitude regions the expected CO mixing ratio of (8 +/- 3) x 10(-4) is measured. Variations of the 2.35-micrometers feature are inconsistent with this value over the Great Martian Volcanoes. If the 2.35-micrometers band is entirely attributable to carbon monoxide, the CO mixing ratio is typically depleted by a factor of 3 over these high altitude areas. Orography should play a major role in the existence of this CO "hole." If, however, these spectral variations at 2.35 micrometers are due to the surface composition, the fraction of the surface covered by the responsible mineral must smoothly decrease as the surface elevation decreases. This phenomenon implies a strong interaction between the surface and the atmosphere for the Great Martian Volcanoes. Diurnal behavior and latitudinal variations of water vapor are globally consistent with Viking measurements. During the Phobos observations, the water vapor amounts over the bright equatorial regions range around 11 pr-micrometers during the day. These amounts are slightly larger than those inferred from 1976 to 1979. The lack of global dust storms during 1988-1989 could explain the enhancement of H2O in the atmosphere.

Astronomy↗

The relative abundance of ethane to acetylene in the Jovian stratosphere.

The observed ratio of C2H6 to C2H2 in the Jovian stratosphere increases from approximately 55 at 2 mbar to approximately 277 at 12 mbar. In current photochemical models this ratio typically increases between 2 and 12 mbar by a factor of < or = 3. Recent laboratory kinetics studies on the reaction between C2H3 and H2 to form C2H4 suggest an efficient chemical mechanism for hydrogenation of C2H2 to C2H6. Inclusion of this scheme as part of a comprehensive updated model for hydrocarbon photochemistry in the atmosphere of Jupiter provides an explanation of the altitude variation of the C2H6/C2H2 ratio. The sensitivity of these results to uncertainties in the key rate constants at low temperatures is illustrated, identifying needs for additional laboratory measurements. Since the key reaction rate constants decrease with decreasing temperature, the hydrogenation of C2H2 as proposed predicts a qualitatively decreasing trend in the C2H6/C2H2 value with decreasing distance from the Sun. The observed variation between Jupiter and Saturn is consistent with this prediction.

Acetylene↗

Hydrocarbon nucleation and aerosol formation in Neptune's atmosphere.

Photodissociation of methane at high altitude levels in Neptune's atmosphere leads to the production of complex hydrocarbon species such as acetylene (C2H2), ethane (C2H6), methylacetylene (CH3C2H), propane (C3H8), diacetylene (C4H2), and butane (C4H8). These gases diffuse to the lower stratosphere where temperatures are low enough to initiate condensation. Particle formation may not occur readily, however, as the vapor species become supersaturated. We present a theoretical analysis of particle formation mechanisms at conditions relevant to Neptune's troposphere and stratosphere and show that hydrocarbon nucleation is very inefficient under Neptunian conditions: saturation ratios much greater than unity are required for aerosol formation by either homogeneous, heterogeneous, or ion-induced nucleation. Homogeneous nucleation will not be important for any of the hydrocarbon species considered; however, both heterogeneous and ion-induced nucleation should be possible on Neptune for most of the above species. The relative effectiveness of heterogeneous and ion-induced nucleation depends on the physical and thermodynamic properties of the particular species, the abundance of the condensable species, the temperature at which the vapor becomes supersaturated, and the number and type of condensation nuclei or ions available. Typical saturation ratios required for observable particle formation rates on Neptune range from approximately 3 for heterogeneous nucleation of methane in the upper troposphere to greater than 1000 for heterogeneous nucleation of methylacetylene, diacetylene, and butane in the lower stratosphere. Thus, methane clouds may form slightly above, and stratospheric hazes far below, their saturation levels. When used in conjunction with the results of detailed models of atmospheric photochemistry, our nucleation models place realistic constraints on the altitude levels at which we expect hydrocarbon hazes or clouds to form on Neptune.

Atmosphere↗

Radiation chemistry in the Jovian stratosphere: laboratory simulations.

Low-pressure continuous-flow laboratory simulations of plasma induced chemistry in H2/He/CH4/NH3 atmospheres show radiation yields of hydrocarbons and nitrogen-containing organic compounds that increase with decreasing pressure in the range 2-200 mbar. Major products of these experiments that have been observed in the Jovian atmosphere are acetylene (C2H2), ethylene (C2H4), ethane (C2H6), hydrogen cyanide (HCN), propane (C3H8), and propyne (C3H4). Major products that have not yet been observed on Jupiter include acetonitrile (CH3CN), methylamine (CH3NH2), propene (C3H6), butane (C4H10), and butene (C4H8). Various other saturated and unsaturated hydrocarbons, as well as other amines and nitriles, are present in these experiments as minor products. We place upper limits of 10(6)-10(9) molecules cm-2 sec-1 on production rates of the major species from auroral chemistry in the Jovian stratosphere, and calculate stratospheric mole fraction contributions. This work shows that auroral processes may account for 10-100% of the total abundances of most observed organic species in the polar regions. Our experiments are consistent with models of Jovian polar stratospheric aerosol haze formation from polymerization of acetylene by secondary ultraviolet processing.

Ammonia↗

Impact-generated atmospheres over Titan, Ganymede, and Callisto.

The competition between impact erosion and impact supply of volatiles to planetary atmospheres can determine whether a planet or satellite accumulates an atmosphere. In the absence of other processes (e.g., outgassing), we find either that a planetary atmosphere should be thick, or that there should be no atmosphere at all. The boundary between the two extreme cases is set by the mass and velocity distributions and intrinsic volatile content of the impactors. We apply our model specifically to Titan, Callisto, and Ganymede. The impacting population is identified with comets, either in the form of stray Uranus-Neptune planetesimals or as dislodged Kuiper belt comets. Systematically lower impact velocities on Titan allow it to retain a thick atmosphere, while Callisto and Ganymede get nothing. Titan's atmosphere may therefore be an expression of a late-accreting, volatile-rich veneer. An impact origin for Titan's atmosphere naturally accounts for the high D/H ratio it shares with Earth, the carbonaceous meteorites, and Halley. It also accounts for the general similarity of Titan's atmosphere to those of Triton and Pluto, which is otherwise puzzling in view of the radically different histories and bulk compositions of these objects.

Atmosphere↗

A physical model of Titan's aerosols.

Microphysical simulations of Titan's stratospheric haze show that aerosol microphysics is linked to organized dynamical processes. The detached haze layer may be a manifestation of 1 cm sec-1 vertical velocities at altitudes above 300 km. The hemispherical asymmetry in the visible albedo may be caused by 0.05 cm sec-1 vertical velocities at altitudes of 150 to 200 km, we predict contrast reversal beyond 0.6 micrometer. Tomasko and Smith's (1982, Icarus 51, 65-95) model, in which a layer of large particles above 220 km altitude is responsible for the high forward scattering observed by Rages and Pollack (1983, Icarus 55, 50-62), is a natural outcome of the detached haze layer being produced by rising motions if aerosol mass production occurs primarily below the detached haze layer. The aerosol's electrical charge is critical for the particle size and optical depth of the haze. The geometric albedo, particularly in the ultraviolet and near infrared, requires that the particle size be near 0.15 micrometer down to altitudes below 100 km, which is consistent with polarization observations (Tomasko and Smith 1982, West and Smith 1991, Icarus 90, 330-333). Above about 400 km and below about 150 km Yung et al.'s (1984, Astrophys. J. Suppl. Ser. 55, 465-506) diffusion coefficients are too small. Dynamical processes control the haze particles below about 150 km. The relatively large eddy diffusion coefficients in the lower stratosphere result in a vertically extensive region with nonuniform mixing ratios of condensable gases, so that most hydrocarbons may condense very near the tropopause rather than tens of kilometers above it. The optical depths of hydrocarbon clouds are probably less than one, requiring that abundant gases such as ethane condense on a subset of the haze particles to create relatively large, rapidly removed particles. The wavelength dependence of the optical radius is calculated for use in analyzing observations of the geometric albedo. The lower atmosphere and surface should be visible outside of regions of methane absorption in the near infrared. Limb scans at 2.0 micrometers wavelength should be possible down to about 75 km altitude.

Atmosphere↗

The photolysis of NH3 in the presence of substituted acetylenes: a possible source of oligomers and HCN on Jupiter.

Photolysis of NH3 in the presence of propyne yields dimethylketazine (4) as the main product along with dimethylketimine, isopropylamine, and propioazine (7). Dimethylketazine and isopropylamine are the principal reaction products when the photolysis is performed at 198 K. The conversion to dimethylketazine is about 35 times greater at 198 K because it is not volatile and condenses on the wall of the photolysis cell out of the UV flux. Photolysis of dimethylketazine at 185 nm yields acetonitrile and small amounts of N-methyldimethylketimine (8). Photolysis of 8 gives acetonitrile. Photolysis of NH3 in the presence of 2-butyne gives the cis and trans isomers of 2-butene as the principal products along with the corresponding azine (9). Photolysis of azine 9 yields acetonitrile and propionitrile. Photolysis of hydrazine in the presence of propyne yields acetonitrile and isopropylamine but no azines were detected as reaction products. Quantum yields and percentage conversion to products are reported. These studies show that acetylenic hydrocarbons formed by the photolysis of methane in the stratosphere of Jupiter may react with radicals formed by NH3 photolysis to give nonvolatile yellow-brown polymers, dialkylazines, alkylnitriles, and eventually HCN. This scenario accounts for the observation of both HCN and chromophores on Jupiter.

Acetonitriles↗

The tropospheric abundances of NH3 and PH3 in Jupiter's Great Red Spot, from Voyager IRIS observations.

To investigate the chemistry and dynamics of Jupiter's Great Red Spot (GRS), the tropospheric abundances of NH3 and PH3 in the GRS are determined and compared to those of the surrounding region, the South Tropical Zone (STZ). These gases well up from deep in the atmosphere, and, in the upper troposphere, are depleted by condensation (in the case of NH3), chemical reactions, and UV photolysis. At Jupiter's tropopause, the chemical lifetimes of NH3 and PH3 are comparable to the time constant for vertical transport over the atmospheric scale height. The distributions of these gases are therefore diagnostic of the rate of vertical transport in the upper troposphere and lower stratosphere. Three groups of Voyager IRIS spectra are analyzed, two of the STZ and one of the GRS. The two groups of STZ spectra are defined on the basis of their radiances at 602 and 226 cm-1, which reflect, respectively, the temperature near 150 mbar and the cloud opacity in the 300-600 mbar region. One selection of STZ spectra is chosen to have the same radiance as does the GRS at 226 cm-1. The other STZ selection has a significantly greater radiance, indicative of reduced cloudiness. Variations in the abundances of NH3 and PH3 are determined within the STZ, as a background for our studies of the GRS. Within the uncertainty of our measurements (-55% and +75%), the PH3 mixing ratio at 600 mbar is 3 x 10(-7), the same for all three selections. The NH3 mixing ratio profile in the pressure region between 300 and 600 mbar is the same within error (-25% and +50% at 300 mbar) for both STZ selections. In the GRS, however, NH3 is significantly depleted at 300 mbar, with an abundance of 25% that derived for the STZ selections. Since the GRS is believed to be a region of strong vertical transport, our finding of a depletion of NH3 below the tropopause within the GRS is particularly unexpected. One of the STZ selections has a temperature-pressure profile similar to that of the GRS below the 300-mbar level; therefore, condensation at this level does not easily explain the low NH3 abundance in the GRS. All samples are taken at essentially the same latitude; photolysis and/or charged particle precipitation is probably not directly responsible either. The observed NH3 depletion may have a dynamical origin or result from some unidentified chemical processes at work in the GRS.

Ammonia↗

A high-precision ab initio determination of the equilibrium geometry and force field of HOC+.

Ab initio molecular orbital theory is used to determine if the molecular ion HOC+ is linear (as are the isoelectronic species HCN, HNC, HCO+, etc.), or if it is quasilinear. Near the Hartree-Fock limit the molecule is either linear, or very close to linear. Electron correlation favors the linear geometry, leading to the unequivocal prediction of a linear molecule. Detailed comparisons between HOC+ and isoelectronic HNC show an apparent lack of convergence in the bending potential for the former which is remedied by the addition of f functions to the basis set. The HOC+ potential energy surface is computed in the bending and bend-stretch coordinates and fit to an analytical function. Use of this function to compute the rotation-vibration energies results in improved agreement with experiment relative to previous potentials by nearly two orders of magnitude, as documented in the accompanying paper.

Astronomical Phenomena↗