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The strong electric dipole-allowed transitions of the molecular ion CO(+) in the region 235-470 GHz have been measured in the laboratory. The laboratory spectra at 235 GHz appear to confirm the claim by Erickson et al. (1981) to have observed CO(+) in OMC-1.
The absorption lines corresponding to the A-X transition of CO have been looked for in the IUE spectra of 14 stars with varying values of the colour excess, E(B-V) and found to be present in the spectra of nine stars with E(B-V) at least 0.28. The column density of CO has been determined towards these nine stars and its upper limit towards the rest of the stars. The curve of growth analysis has been found to show that the contribution to CO absorption is possibly from a single interstellar cloud for stars with E(B-V) less than 0.4 and from more than one cloud for stars with E(B-V) greater than 0.4. The observed column density of CO as a function of E(B-V) has been found to be in good agreement with that expected from the theory of ion-molecular chemistry.
Atoms, molecules, and atomic and molecular ions generated by solar wind interactions with dust grains of the zodiacal cloud are discussed. The main processes leading to the generation of these particles are described and relevant methods of observation are examined.
The paper presents some initial results on measurements of the thermal plasma environment obtained by a spherical retarding potential analyzer and a Langmuir probe flown on (STS-3) as part of the NASA Office of Space Science-1 payload in March 1982. One of the major effects observed is a higher degree of turbulence in the ambient plasma compared to what is observed from similar instruments flown on unmanned satellites. In addition we see the temperature of the thermal electrons elevated to values of 4000-5000 K. Associated with elevated electron temperatures are regions of enhanced plasma density resulting from the appearance of high densities of molecular ions. The thermal plasma data also show clear effects of an induced V x B.L potential at the location of the probes which matches that produced by an L vector linking the probes to the engine nozzles; thereby establishing the prime return current location on the Orbiter. The final observations discussed are the pronounced and complex wake effects resulting both from the main structure of the Orbiter and from the complex shapes of appendages attached to the Orbiter.
Recent laboratory spectroscopic results on the transient neutral species CCH, NH2, and NaH, the molecular ions HCO(+), N2H(+), and CO(+), and the light asymmetric internal rotor HOOH are reviewed. It is shown that the shorter millimeter and submillimeter spectral region offers a number of advantages, even in the laboratory. Attention is also given to the requirements for theoretical models capable of the accurate spectral predictions required for many astrophysical applications. The results presented here are seen as demonstrating that millimeter and submillimeter microwave spectroscopy provides a sensitive and flexible means of studying short-lived species in the laboratory. It is believed that, in combination with the appropriate theoretical approach, studies of this type are capable of providing accurate spectral maps over wide spectral regions for most species of astrophysical importance.
The spatial and compositional distribution of the thermal plasma in the magnetosphere of Saturn is described in the light of the Voyager encounters. Theoretical considerations are applied to the elucidation of the structure, including two external and two internal boundaries. The outer boundary is a magnetohydrodynamic entity, while the inner boundary of locally created thermal plasma is a result of the dissociative recombination of corotating molecular ions. The internal boundaries, which separate plasmas of different composition, are explained as a charge exchange quasi-resonance phenomenon.
The imaging spectrometric observatory (ISO) is discussed. The objectives of this instrument are to measure the spectral signatures of a large range of minor constituents, metastable, and excited species of both atomic and molecular ions, and neutrals in the atmosphere (from the stratosphere to the upper thermosphere). The instrument is composed of five identical spectrometers, each restricted to a given spectral range between 20 and 1200 nanometers designed for high speed operation as an imaging device. Each module is an imaging scanning spectrometer with coincident 0.5 x 0.007 degree field of view.
The development of techniques for the calculation of electron capture widths, electronic wave functions, cross sections and rates needed for the description of the dissociative recombination (DR) of molecular ions with electrons were described. The cross sections and rates were calculated by using harmonic oscillator wave functions for the ion and a delta function approximation for the continuum vibrational wave function in the repulsive dissociative channel. In order to obtain DR cross sections of quantitative accuracy, a computer program which solves the one dimensional nuclear motion wave equation was revised to calculate the cross sections and rates. The program and the new results are described. Included is a discussion of large windows found in the dissociative recombination cross sections from excited ion vibrational levels. These windows have not been previously reported in the literature. The magnitude of the DR cross sections for several dissociative routes are sensitive to the location of the crossing of the neutral and ion potential curves. Studies of the effects of basis set and CI wave function size on vertical excitation energies are described. Preliminary studies on N2 and O2 using large scale wave functions are also reported.
The imaging spectrometric observatory (ISO) is discussed. The objectives of this instrument are to measure the spectral signatures of a large range of minor constituents, metastable, and excited species of both atomic and molecular ions, and neutrals in the atmosphere (from the stratosphere to the upper thermosphere). The instrument is composed of five identical spectrometers, each restricted to a given spectral range between 20 and 1200 nanometers designed for high speed operation as an imaging device. Each module is an imaging scanning spectrometer with coincident 0.5 x 0.007 degree field of view.
The winter anomaly of radio wave absorption in the ionospheric D region (65 to 90 km), caused by a factor of about ten increase in electron density, has been considered to be due to a factor of about ten increase of the nitric oxide concentration and/or a few tens of degrees Kelvin temperature rise due to a strong temperature dependency of the conversion rate of molecular ions to cluster ions. In order to investigate the mechanism of the winter anomaly, the processes that brought about these changes are identified. It is well known that stratospheric warmings sometimes accompany the winter anomaly in middle latitudes. The present study concentrates on the winter anomaly which occurred simultaneously during a sudden warming of the 1967 to 1968 winter, from middle December 1967 to middle January 1968. Variations of geophysical and ionospheric parameters are shown.
The application of a recently described technique for producing significantly enhanced concentrations of molecular ions for spectroscopic study to the detection and measurement of the millimeter and submillimeter wave spectrum of CF(+) is reported. The experimental procedure is discussed, and the measured absorption frequencies are shown and compared with those calculated from spectral constants. These constants are given together with those from the infrared spectrum by Kawaguchi and Hirota (1985).
The deuterated cyclopropenylidene ring molecule, C3HD, has been detected toward several sources in four rotational lines, at 19, 79, 104, and 107 GHz. The relative integrated intensities of the 2-sub-12 - 1-sub-01 lines of C3HD and C3H2 are found in the ratio 1:5, indicating a high deuterium fractionation ratio for cyclopropenylidene. The detection of the C-13 isotope of C3H2 at the same position allows a determination of the optical thickness (about 3) of the line. The detection of such a large enhancement in the deuterated form of C3H2 very strongly suggests that a molecular ion is the chemical precursor of the molecules. Consideration of the amount of the enhancement relative to that in other molecules suggests that the precursor ion is C3H3+.
Model potential curves are used to show that large windows are present in direct dissociative-recombination cross sections from excited molecular-ion vibrational levels. The windows are due to the overlap of vibrational wave functions of the repulsive neutral states with the nodes of the ion vibrational wave function.
Attempts to measure the ambient ionospheric plasma environment in the vicinity of the payload bay of the Space Shuttle Orbiter have shown that the plasma is quite different, in a variety of characteristics, from the ionospheric plasma at low earth orbit altitudes. It appears that the large size, complex geometry and various outgassing characteristics of a typical Orbiter payload can all contribute to modifications of the plasma environment of the Space Shuttle Orbiter. The measurements indicate that the plasma is often quite turbulent and contains populations more energetic than the ambient ionospheric plasma. Pronounced wake and ram effects have been observed, and at times the data can be interpreted as plasma number density enhancements of an order of magnitude or greater over the ambient, undisturbed plasma concentration. There is evidence that this enhanced plasma concentration contains molecular ions, not occurring naturally at low earth orbit altitudes. In addition to describing the observations, the electrodynamics of enhanced Orbiter-generated plasma and its possible impact on optical measurements from the Space Shuttle Orbiter will be discussed.
An interpretation of the variation of rate constants with vibrational temperature is proposed which introduces parameters analogous to those of the classical Arrhenius expression. The constancy of vibrational activation energy is studied for the dissociaton of NO, the ion-molecular reaction of O(+) with N2, and the atom exchange reaction of I with H2. It is found that when a Boltzmann distribution for vibrational states is applicable, the variation of the rate constant with the vibrational temperature can be used to define a vibrational activation energy. The method has application to exchange reactions where a vibrational energy threshold exists.
Observations of NH2, (OI) and molecular ion spectra in comets represent virtually all of the volatile fraction of a comet nucleus. Their study leads to the N2, NH3, H2O, CO2, CO content of the nucleus, and thus to important constraints on models of comet formation and chemical processing in the primitive solar nebula. The observations of Comet Halley provide the opportunity for the first comprehensive determination of the abundances in a comet nucleus. The carbon isotope abundance ratio 12 C/13 C = 65 plus or minus 8 has been determined for Comet Halley from resolved rotational line structure in the CN B-X (0,0) band. The ratio is approximately 30 pct lower than the solar system value, 89, indicating either an enhancement of 13CN or a depletion of 12CN in the comet. Scenarios consistent with the observed carbon isotope ratio are: (1) formation of the comet at the periphery of the solar nebula in a fractionation-enriched 13CN region, or hidden from 12CN enrichment sources, and (2) capture of an interestellar comet. Long-slit charge coupled device (CCD) spectra obtained at the time of the spacecraft encounter of Comet Halley have also been analyzed. Scale lengths, production rates and column densities of CH, CN, C2 and NH2 were determined.
Dissociative recombination (DR) of molecular ions with electrons has important consequences in many areas of physical science. Ab-initio calculations coupled with resonant scattering theory and multichannel quantum defect studies have produced detailed results illuminating the role of ion vibrational excitation, the quantum yields of the DR products, and the role of Rydberg states. The theoretical and experimental results are discussed.
Deexcitation rates, lifetimes, and branching ratios are calculated for all the J = 0, J = 1, and J = 2 bound states of the muonic molecular ion td(mu) when it serves as the nucleus of a hydrogen atom. The J = 2 binding energy (E2 = 101.59 eV) is the first reported variational result for this state. It is found that the excited J = 0 state is populated several hundred times as often as the ground state.