Publications by authors named "DC Benner"

Retrievals of atmospheric composition from near-infrared measurements require measurements of airmass to better than the desired precision of the composition. The oxygen bands are obvious choices to quantify airmass since the mixing ratio of oxygen is fixed over the full range of atmospheric conditions. The OCO-2 mission is currently retrieving carbon dioxide concentration using the oxygen A-band for airmass normalization.

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Using 0.002 cm(-1) resolution Fourier transform absorption spectra of an (17)O enriched ozone sample, an extensive analysis of the v(1)+v(3) bands of the (16)O(17)O(16)O and (16)O(16)O(17)O isotopomers of ozone has been performed for the first time. The experimental rotational levels of the (101) vibrational states were satisfactorily reproduced using a Hamiltonian matrix that takes into account the observed rovibrational resonances.

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High-resolution Fourier transform absorption spectra of ozone broadened by dry air have been recorded at a number of temperatures from -63°C to 29°C. Using a multispectrum nonlinear least-squares procedure, we fit 29 of these spectra simultaneously to determine the air-broadening and shift coefficients and their temperature dependences for 450 lines in the 9-&mgr;m region; most of these belong to the nu1 band. Partial air-broadening results were obtained for 104 additional lines, and room-temperature self-broadening coefficients were also determined for most of the 554 lines measured.

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Room temperature measurements of self- and air-broadening coefficients are reported for over 370 transitions covering a range of 0 View Article and Find Full Text PDF

Air-, nitrogen-, and oxygen-broadened halfwidth and pressure-induced line shift coefficients have been measured for over seventy-five individual vibration-rotation transitions in the v(3) fundamental band of (13)CH(4)at 3 mum from room temperature IR laboratory absorption spectra recorded at a 0.01-cm(-1) resolution with a Fourier transform spectrometer. Transitions up to J" = 13 in the P-branch and J" = 7 in the R-branch were analyzed using a nonlinear least-squares curve fitting technique assuming a Voigt line shape.

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Room temperature argon broadened halfwidth and pressure-induced line shift coefficients have been determined for 118 transitions in the nu(4) band of (12)CH(4) from analysis of high resolution laboratory absorption spectra recorded with the McMath Fourier transform spectrometer operated on Kitt Peak by the National Solar Observatory. Transitions up to J''= 12 have been measured using a nonlinear least-squares spectral fitting procedure. The variation of the measured halfwidth coefficients with symmetry type and rotational quantum number is very similar to that measured previously for N(2) and air broadening, but the absolute values of the argon broadening coefficients are all smaller.

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Air-broadened halfwidths and pressure-induced line shifts in the nu(4) fundamental of (13)CH(4) were determined from spectra recorded at room temperature and at 0.01-cm(-1) resolution using a Fourier transform spectrometer. Halfwidths and pressure shifts were determined for over 180 transitions belonging to J''values of View Article and Find Full Text PDF

Absolute intensities for 430 transitions belonging to eleven rotation-vibration bands of (12)C(16)O(2),(13)C(16)O(2) and(16)O(12)C(18)O in the 3140-3410-cm(-1) spectral region have been determined by analyzing spectra recorded at 0.01-cm(-1) resolution with the Fourier transform spectrometer in the McMath solar telescope complex at the National Solar Observatory on Kitt Peak. The data were recorded at room temperature and low pressures (<10 Torr) using a natural sample of carbon dioxide.

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Air-broadened and N(2)-broadened halfwidth and pressure shift coefficients of 294 transitions in the nu(4) and nu(2) bands of (12)CH(4) have been measured from laboratory absorption spectra recorded at room temperature with the Fourier transform spectrometer in the McMath solar telescope facility of the National Solar Observatory. Total pressures of up to 551 Torr were employed with absorption paths of 5-150 cm, CH(4) volume mixing ratios of 2.6% or less, and resolutions of 0.

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Air-broadened and N2-broadened halfwidths at room temperature for twenty-five transitions in the 4 fundamental band of '2CH4 have been determined from IR absorption spectra recorded with a tunable diode laser spectrometer. Two tunable diode lasers operating in the 1250-1380-cm(-1) region were used to obtain these data. Air-broadened halfwidths for twenty of these lines were also determined from additional spectra recorded at 0.

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A nonlinear least-squares spectral fitting procedure has been used to derive experimental absolute intensities for over 300 unblended lines belonging to twelve bands of (12)C(16)O2, (13)C(16)O2, (16)O(12)C(18)O, (16)O(12)C(17)O, and (16)O(13)C(18)O in the 5.2-microm region. The spectral data were recorded at 0.

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A nonlinear least-squares fitting procedure has been used to derive absolute intensities for lines in the P, R, and Q branches of the (11(1)0)II <-- 00(0)0 band of 12Cl602 (band center = 1932 cm(-1)) from long-path 0.01-cm(-1) resolution laboratory spectra. The spectral data were recorded at room temperature and low pressure (<10 Torr) with the Fourier transform spectrometer in the McMath solar telescope complex at Kitt Peak National Observatory.

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