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Rinsland, C. P.

Publications and source records attributed to Rinsland, C. P..

At least 91 records · Page 5
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NASA NTRS1993

The nu(sub 2) and 2nu(sub 2) - nu(sub 2) bands of N-14 (16)O2: Electron Spin-Rotation and Hyperfine Contact Resonances in the (010) Vibrational State

High-resolution Fourier transform spectra covering the 720-9-10/ cm spectral region have been used to perform a reanalysis of the 2nu(sub 2) band ((010) - (000) vibrational transition) together with the first analysis of the nu(sub 2) - nu(sub 2) hot band of nitrogen dioxide ((020)-(010) vibrational transition). The high-quality spectra show that, for numerous nu(sub 2) lines, the hyperfine structure is easily observable in the case of resonances due to the hyperfine Fermi-type operator. By performing a full treatment of the spin-rotation and of the hyperfine operators, a near line list of the nu(sub 2) band (positions and intensities) has been generated, and it is in excellent agreement with the experimental spectrum. Also, a thorough analysis of the -2nu(sub 2) nu(sub 2) hot band has been performed leading to an extended set of new (020) spin-rotation levels, These levels, together with the (100), (020), (001) spin-rotation levels deduced previously from the analysis of thenu(sub 1), 2nu(sub 2), and nu(sub 3) cold bands performed in the 6.3 - to 7.5 microns spectral range were least-squares fitted, allowing one to derive a new set of vibrational band centers and rotational. spin-rotation, and interaction constants for the {(100)(020)(001)} interacting states of N-14(16)O2.

Perrin, A.↗
NASA NTRS1993

Stratospheric N2O5, CH4, and N2O Profiles from IR Solar Occultation Spectra

Stratospheric volume mixing ratio profiles of N2O5, CH4, and N2O have been retrieved from a set of 0.052/ cm resolution (FWHM) solar occultation spectra recorded at sunrise during a balloon flight from Aire sur I'Adour, France (44 deg N latitude) on 12 October 1990. The N2O5 results have been derived from measurements of the integrated absorption by the 1246/ cm band. Assuming a total intensity of 4.32 x 10(exp 17)cm(exp -1) molecule sq cm(exp -2) independent of temperature, the retrieved N2O5 volume mixing ratios in ppbv (parts per billion by volume, 10(exp -9)), interpolated to 2 km height spacings, are 1.64 +/- 0.49 at 37.5 km, 1.92 +/- 0.56 at 35.5 km, 2.06 +/- 0.47 at 33.5 km, 1.95 +/- 0.42 at 31.5 km, 1.60 +/- 0.33 at 29.5 km, 1.26 +/- 0.28 at 27.5 km, and 0.85 +/- 0.20 at 25.5 km. Error bars indicate the estimated I-sigma uncertainty including the error in the total band intensity (+/- 20% has been assumed). The retrieved profiles are compared with previous measurements and photochemical model results.

Peyeret, C. Camy↗
NASA NTRS1992

Middle and upper atmosphere pressure-temperature profiles and the abundances of CO2 and CO in the upper atmosphere from ATMOS/Spacelab 3 observations

An improved method for retrieving pressure-temperature profiles is described and is used to retrieve profiles of the kinetic-temperature and atmospheric-pressure profiles between 20 and 116 km altitudes and the CO2 and CO volume-mixing ratios between 70 and 116 km, using the IR occultation spectra recorded by the Spacelab 3 atmospheric trace molecular spectroscopy (ATMOS) Fourier transform spectrometer between April 29 and May 6, 1985. Profiles are derived for six ATMOS occultations. The CO2 and CO volume-mixing profiles are compared with previous observations and model predictions. Evidence is found for vibrational non-LTE by analyzing the lines of the (nu-2 + nu-3 - nu-2) (C-12)(O-16) band. Results are used for deriving (C-12)(O-16) (010) vibrational temperatures, which are compared with the retrieved kinetic temperatures and the predictions of non-LTE effects by recent models.

Rinsland, C. P.↗
NASA NTRS1992

The HITRAN molecular data base - Editions of 1991 and 1992

We describe in this paper the modifications, improvements, and enhancements to the HITRAN molecular absorption database that have occurred in the two editions of 1991 and 1992. The current database includes line parameters for 31 species and their isotopomers that are significant for terrestrial atmospheric studies. This line-by-line portion of HITRAN presently contains about 709,000 transitions between 0 and 23,000/cm and contains three molecules not present in earlier versions: COF2, SF6, and H2S. The HITRAN compilation has substantially more information on chlorofluorocarbons and other molecular species that exhibit dense spectra which are not amenable to line-by-line representation. The user access of the database has been advanced, and new media forms are now available for use on personal computers.

Rothman, Laurence S.↗
NASA NTRS1992

Improved spectroscopic line parameters for the ozone molecule

Recently available spectral O3 line parameters are summarized and progress in remote sensing based on these parameters is discussed. Particular attention is given to covering line positions, line intensities and linewidths for both the main isotopic species (O-16)3 and the isotopic variants (O-16)(O-18)(O-16) and (O-16)(O-16)(O-18).

Flaud, J.-M.↗
NASA NTRS1992

The 1985 chlorine and fluorine inventories in the stratosphere based on ATMOS observations at 30 deg North latitude

Results are presented of an investigation of the Cl and F inventories derived from the concentrations of eleven Cl- and F-bearing organic and inorganic species throughout the atmosphere, based on observations with the Atmospheric Trace Molecule Spectroscopy instrument aboard the Space Shuttle during the Spacelab 3 mission of April 29 to May 6, 1985. It was found that, in April-May 1985, near 30 deg N, the mean total stratospheric concentrations of Cl and F were 2.58 +/-0.10 ppbv and 1.15 +/-0.12 ppbv, respectively. Partitioning among the source, sink, and reservoir species was consistent with the conservation of the F and Cl budgets throughout the stratosphere. It is shown that the budgets of Cl and F above about 45 km altitude can be determined accurately by measuring only HCl, HF, and CF4 and provide a straightforward timely reference point for future inventories and trends evaluations.

Zander, R.↗
NASA NTRS1992

Ground-based infrared measurements of carbonyl sulfide total column abundances - Long-term trends and variability

Attention is given to total vertical column abundances of carbonyl sulfide (OCS) derived from time series of high-resolution IR solar absorption spectra recorded near Tucson, Arizona, and in the Swiss Alps. The analysis of both data sets is based on nonlinear least squares spectral fittings of narrow intervals centered on lines of the intense nu3 band of OCS, the P(37) transition at 2045.5788/cm, and the P(15) transition at 2055.8609/cm, with a consistent set of spectroscopic line parameters. The Arizona measurements, recorded on 20 different days between May 1977 and March 1991, show a 10-percent peak-to-peak seasonal cycle with a summer maximum and a winter minimum and a trend in the total column abundance equal to (0.1 +/-0.2) percent/yr, 2sigma. The Alpine total columns exhibit a more complex seasonal variation than noted in the Arizona data. The results from the two sites indicate that there has been no significant change in the OCS total column abundance at northern midlatitudes over the last decade.

Rinsland, C. P.↗
NASA NTRS1992

Stratospheric HNO3 measurements from 0.002/cm resolution solar occultation spectra and improved spectroscopic line parameters in the 5.8-micron region

Very-high-resolution FWHM solar-occultation spectra are investigated with a balloon-borne interferometer using revised spectroscopic line parameters for HNO3, O3, and H2O. The O3 and H2O data are evaluated to determine their capacity for interference in the HNO3 line which is studied in the nu sub 2 band at 5.8 microns. The line parameters developed with the stratospheric data are compared to data based on a HITRAN compilation as well as laboratory spectra with a 0.002/cm resolution. The line list is calculated and shown to include J and Ka transitions which improve the line parameters for HNO3 by accounting for the weaker absorption features in the stratospheric spectra. The stratospheric HNO3 profile developed analytically is compared to those based on reported measurements, and the one developed with the stratospheric solar spectra is found to be consistent with the measurements and confirm inherent measurement biases.

Goldman, A.↗
NASA NTRS1992

Mt. Pinatubo SO2 column measurements from Mauna Loa

Absorption features of the nu sub 1 band of SO2 are identified in high-resolution IR solar-absorption spectra recorded from Mauna Loa, Hawaii, on July 9 and 12, 1991, shortly after the arrival of the first eruption plume from the Mt. Pinatubo volcano. A total SO2 vertical column amount of (5.1 +/- 0.5) x 10 exp 16 molecules/sq cm on July 9 is retrieved based on nonlinear least-squares spectral fittings of 9 selected SO2 absorption features with an updated set of SO2 spectral parameters. A SO2 total-column upper limit of 0.9 x 10 exp 16 molecules/sq cm deduced from measurements on September 20-24, 1991, is consistent with the dispersion of the SO2 cloud and the rapid conversion of the SO2 vapor into volcanic aerosol particles.

Goldman, A.↗
NASA NTRS1992

Mt. Pinatubo SO2 Column Measurements From Mauna Loa

Absorption features of the nu(sub 1) band of SO2 have been identified in high resolution infrared solar absorption spectra recorded from Mauna Loa, Hawaii, on July 9 and 12, 1991, shortly after the arrival of the first eruption plume from the Mt. Pinatubo volcano in the Phillipines. A total SO2 vertical column amount of (5.1 +/- 0.5) x 10(exp 16) molecules/sq cm on July 9 has been retrieved based on nonlinear least- squares spectral fittings of 9 selected SO2 absorption features with an updated set of SO2 spectral parameters. A SO2 total column upper limit of 0.9 x 10(esp 16) molecules/sq cm deduced from measurements on September 20-24, 1991, is consistent with the dispersion of the SO2 cloud and the rapid conversion of the SO2 vapor into volcanic aerosol particles.

Goldman, A.↗
NASA NTRS1991

Vertical column abundances and seasonal cycle of acetylene, C2H2, above the Jungfraujoch station, derived from IR solar observations

Results derived from a spectroscopic analysis of the nu5 band R19 transition of C2H2 observed in solar spectra recorded at the Jungfraujoch station, Switzerland, between June 1986 and April 1991 are reported. A least-squares sine fit to the data reveals a seasonal variability with an amplitude of about +/-40 percent of the mean; the maximum occurs during mid-winter and the minimum in summer. In general, the observed seasonal observations are comparable with those derived from airborne in-situ measurements and those reported from ground-based stations.

Zander, R.↗
NASA NTRS1991

Infrared spectroscopic measurements of the vertical column abundance of sulfur hexafluoride, SF6, from the ground

The solar observations involved in the present monitoring evaluation were made at two facilities, using Fourier-transform spectrometers achieving spectral resolutions of 0.005/cm and signal-to-rms noise ratios for individual scans from near 500 to near 1000. The monthly mean total vertical-column abundances of SF6 above both facilities are reported for time intervals from June 1986 to June 1990 and from March 1981 to June 1990. It is found that the vertical-column abundances increased at mean rates of 6.9 +/- 2.8 pct above one station and 6.6 +/- 7.2 pct above the other. Since all the results were retrieved using the same spectroscopic parameters and similar nonlinear least-squares curve-fitting algorithms validated through intercomparison exercises, the large error reported for the second station is attributed to a larger measurement uncertainty due to stronger H2O and C2O interferences, and a greater variability during each month.

Zander, R.↗
NASA NTRS1991

Infrared measurements of HF and HCl total column abundances above Kitt Peak, 1977-1990 - Seasonal cycles, long-term increases, and comparisons with model calculations

The paper deals with hydrogen-chloride and hydrogen-fluoride total column measurements, their estimated long-term rates of increase, seasonal cycles, and variability, deduced from the analysis of a set of high-resolution infrared solar spectra recorded at Kitt Peak. The Kitt Peak observations and methods of analysis are described, the results are presented and compared with previously reported measurements and trends. The data is analyzed by using a multilayer nonlinear least-squares spectral fitting procedure and a consistent set of spectroscopic line parameters. Model-calculated hydrogen-chloride and hydrogen-fluoride total columns obtained with a two-dimensional model are discussed, and the model results are compared with the measured hydrogen-chloride and hydrogen-fluoride total columns, seasonal cycles, and trends. It is pointed out that the observed trends of both molecules are in satisfactory agreement with the model results calculated from emission histories and photooxidation rates for the source molecules.

Rinsland, C. P.↗
NASA NTRS1991

Determination of absolute strengths of N2 quadrupole lines from high-resolution ground-based IR solar observations

The strength of S-branch lines of the N2 (1-0) electric quadrupole vibration-rotation band are determined by an analysis of solar absorption spectra. The solar data were recorded with a Fourier transform spectrometer and are characterized by high resolution, and a high signal-to-noise ratio. By extrapolating equivalent width measurements of the lines from varying air masses to zero air mass, the line strengths are found for the transitions from S7 to S10. The results presented do not include half widths and are found to be accurate to within 5 percent, and following a redetermination the N2 transitions are accurate to within 0.0002/cm. Line-of-sight atmospheric air masses associated with remotely sensed IR spectroscopic observations can be determined directly by utilizing the highly accurate data.

Demoulin, P.↗
NASA NTRS1991

Improved spectroscopic line parameters for the ozone molecule

Recently the authors made a comprehensive compilation of improved line positions, intensities, and lower state energies of ozone between 0 and 3400/cm. Examples of improvement brought by these data and progress achieved in remote sensing using them are given. Areas for future study include hot bands in the higher wavenumber range, spectral regions above 3400/cm, the O-17 isotopic variants of ozone, broadening coefficients, and emission from high-lying vibrational levels of ozone in the upper atmosphere.

Flaud, J. M.↗
NASA NTRS1991

Ground-based infrared measurements of HNO3 total column abundances - Long-term trend and variability

The long-term trend and variability of the total column amount of atmospheric nitric acid (HNO3) have been investigated. The study was based on time series of infrared solar absorption spectra recorded at two sites, the International Scientific Station of the Jungfraujoch (ISSJ) in the Swiss Alps (altitude 3.6 km, latitude 46.5 N, longitude 8.0 E) and the National Solar Observatory McMath solar telescope facility on Kitt Peak (altitude 2.1 km, latitude 31.9 N, longitude 111.6 W), Arizona. Measurements of HNO3 absorption features recorded at Kitt Peak between 1980 and 1990 and measurements of the same features in ISSJ solar spectra obtained in June 1951 and June 1986 to June 1990 provide quantitative estimates of the long-term trend in the HNO3 total vertical column. It is found that the trend deduced for each site is equal to zero within the measurement uncertainty. The modern ISSJ measurements show that the fitted trend is (-0.16 + or - 0.50) percent/yr, 2 sigma, which indicates that there has been no detectable change in HNO3 total column over three decades. The Kitt Peak measurements show marked variability in the HNO3 total column, but no obvious seasonal cycle is observed.

Rinsland, C. P.↗