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Fox, K.

Publications and source records attributed to Fox, K..

At least 37 records · Page 2

Two new methanol transitions in Orion A

Emission from the 11(1) - 10(2) (A-) and 5(0) - 4(1) (E) transitions of CH3OH at rest frequencies of 76,247.4 and 76,509.9 MHz, respectively, has been detected toward Orion A. The velocity widths of the two transitions are estimated to be approximately 3 km/s, which is consistent with other methanol lines in Orion. It is noted that the 117.5-kayser upper-state energy of the 11(1) - 10(2) (A-) transition is the highest yet reported for methanol in any source. The observed intensity is shown to be consistent with the 90-K thermal excitation model that seems to be appropriate for all other reported CH3OH lines in Orion A. Total column densities of 3 x 10 to the 16th per sq cm for the 11(1) - 10(2) (A-) transition and of 2 x 10 to the 16th per sq cm for the 5(0) - 4(1) (E) transition are calculated.

Jennings, D. E.

Methane detected in Orion A

This letter reports the detection of line emission from the Orion Molecular Cloud corresponding to six distinct pure-rotational delta J = 0 transitions in CH4. The transitions observed and the transition frequencies are: J = 11 E(2) - E(1), 4600.359 MHz; J = 18 F1(4) - F2(1), 76,231.45 MHz; J = 18 A1(2) - A2(1), 76,700.02 MHz; J = 19 F1(4) - F2(1), 75,944.99 MHz; J = 19 F2(4) - F1(1), 78,233.59 MHz; and J = 20 F2(5) - F1(2), 82,873.59 MHz. The observed spectra at the six transition frequencies are plotted, and all but two of the methane lines are found to be very narrow (about 2 km/s). It is noted that the small velocity widths of the four weaker lines and an observed variability of the J = 18 A line are classic characteristics of a maser and that the excitation appears to be nonthermal. An effective excitation temperature of 1100 to 2100 K is estimated for the methane in Orion A.

Fox, K.

High-resolution infrared spectra of v sub 3 and 2v sub 3 of germane

Band origins, secondary (or satellite) lines, and intensity anomalies are discussed for the infrared spectra of v sub 3 and 2v sub 3 of germane. Germane has been tentatively identified as spectroscopically active in the atmosphere of Jupiter. The molecule is also of interest for studies of isotope shifts in spherical-top spectra such as those measured in methane at 6000 kaysers.

Daunt, S. J.

Possible Jovian methane emission at 76 GHz in coincidence with decameter activity

The tentative detection of a methane line in emission at 76.2 GHz in the atmosphere of Jupiter is reported. The observed feature is well-correlated with the presence and absence of Jovian decameter-emission activity on successive days. The present results may represent the first detection of extraterrestrial methane microwave emission.

Fox, K.

Isotope shifts in methane near 6000/cm

Isotope shifts for cleanly resolved vibrational-rotational absorption lines of CH4-12 and CH4-13 were measured by a 5-m focal length Littrow spectrometer in the 6000/cm range. The methane isotopes were held in separate absorption cells: 20 torr of CH4-13 in a 1-m cell, and 5 torr of CH4-12 in a White cell of 4-m optical path length. Measured shifts for the cleanly resolved singlets R(0), R(1), Q(1) and P(1) are summarized in tabular form.

Fox, K.

On the 23-micron feature in the spectrum of Jupiter

The spectroscopic activity of gaseous constituents in the Jovian atmosphere is investigated with a view toward absorption at 23 microns. Various possibilities for the source of this feature are excluded, particularly pressure-induced dipole transitions involving collisions between H2 and either CH4 or HD.

Fox, K.

nu sub 1 + nu sub 3 combination band of S-32 O2-16.

The infrared-active vibration-rotation band nu sub 1 + nu sub 3 of sulfur dioxide has been measured with moderately high spectral resolution. Quantum number identifications of spectral lines were made by comparison with theoretically computed spectra which include the effects of centrifugal distortion. The band center for nu sub 1 + nu sub 3 was determined to be 2499.60 plus or minus 0.10 per cm. An absolute band intensity has also been measured in this work, and the magnitude of the dipole moment derivative was evaluated.

Corice, R. J., Jr.

Nu sub 1 plus nu sub 3 combination band of SO2

The infrared-active vibration-rotation combination band nu sub 1 + nu sub 3 of sulfur dioxide was measured with moderately high spectral resolution. Quantum number identifications of spectral lines were made by comparison with theoretically computed spectra which include the effects of centrifugal distortion. Relative line intensities were also calculated. The band center for nu sub 1 + nu sub 3 was determined to be 2499.60 + or - 0.10/cm.

Corice, R. J., Jr.

A tentative identification of /C-13/H4 and an estimate of C-12/C-13 in the atmosphere of Jupiter.

Laboratory spectra of the 3nu(sub 3) band of (C-13)H4 at 1.1 micron were analyzed along with high-resolution image-tube spectra of Jupiter in the appropriate spectral region. Comparison of several J-multiplets in these spectra resulted in the identification of (C-13)H4 in the atmosphere of Jupiter. A Jovian C-12/C-13 isotopic abundance ratio of 110 (plus or minus 35) has been derived from the equivalent width of the R(2) multiplet measured on the two best spectrograms.

Fox, K.

Fundamental bands of S(32)O2(16)

The infrared-active vibration-rotation fundamentals of sulfur dioxide were measured with moderately high spectral resolution. Quantum number assignments were made for spectral lines from J = O to 57, by comparison with theoretically computed spectra which include the effects of centrifugal distortion. The following values for the band centers were determined: nu sub 1 = 1151.65 + or - 0.10/cm, nu sub 2 = 517.75 + or - 0.10/cm, and nu sub 3 = 1362.00 + or - 0.10/cm. Intensities of the observed lines have also been computed. Dipole moment derivatives were obtained.

Fox, K.