Engineering topics
Publications and source records attributed to Carli, B..
This viewgraph presentation describes the Global Hawk aircraft and its unique performance capabilities as it pertains to the study of the climate change.
The calibration of high resolution infrared spectra is generally more precise than accurate even when they are recorded with Fourier interferometers. In order to improve the consistency of the spectral measurements, an IUPAC project has been undertaken. Its aim was to recommend a selection of spectral lines as wavenumber standards for absolute calibration in the infrared. This paper will report the final recommendations in the spectral range extending from about 4 to about 7000 cm(be).
The calibration of high resolution infrared spectra is generally more precise than accurate. This is the case even when they are recorded with Fourier transform interferometers. This presentation aims at improving the accuracy of wavenumber measurements in the infrared by recommending a selection of spectral lines as wavenumber standards for absolute calibration.
Stratospheric concentrations of HO2, H2O2, and OH have been retrieved simultaneously from the far-infrared emission spectra obtained with a balloon-borne Fourier transform spectrometer in June 1983 at 32 deg N latitude. Retrieved concentrations of HO2 and H2O2 are reported, along with vertical distributions of OH which were reported in an earlier paper for the afternoon, sunset, and nighttime periods for altitudes from 26 to 38 km. HO2 distributions are obtained with uncertainties that are about the same as OH for the same vertical range and for the afternoon and sunset periods. H2O2 concentration is obtained at an altitude of 30 km for the period that covers afternoon and sunset hours. The retrieved concentrations of these HO(x) species agree well with other individually measured results and the steady state photochemical predictions. The ratio HO2/OH at around 32 km seems to increase from the afternoon period to the sunset period.
Observations of the vertical profile of hydrogen fluoride (HF) vapor in the stratosphere and of the vertical column amounts of HF above certain altitudes were made using a variety of spectroscopic instruments in the 1982 and 1983 Balloon Intercomparison Campaigns. Both emission instruments working in the far-infrared spectral region and absorption instruments using solar occultation in the 2.5-micron region were employed. No systematic differences were seen in results from the two spectral regions. A mean profile from 20 - 45 km is presented, with uncertainties ranging from 20 to 50 percent. Total columns measured from ground and from 12 km are consistent with the profile if the mixing ratio for HF is small in the troposphere and low stratosphere.
The balloon-borne instruments used in the two Balloon Intercomparison Campaigns in 1982 and 1983 to measure stratospheric HCl included five different IR spectrometers, three of which operated in the solar absorption mode and two in emission mode (at distinctly different wavelengths). This paper describes the instruments and the data reduction and analysis procedures used in each case, together with the sources and estimated magnitudes of associated errors. Comparisons are made between different techniques (absorption vs emission) used on the same gondola, as well as between the same technique used on different gondolas. The final results yield a mean profile of HCl concentration between 18 and 40 km altitude. The absolute accuracy of the final profile is estimated to be no worse than 10 percent.
Emission features of HBr isotopes have been identified in high-resolution FIR emission spectra obtained with a balloon-borne Fourier-transform spectrometer in the spring of 1979 at 32 deg N latitude. When six single-scan spectra at a zenith angle of 93.2 deg were averaged, two features of HBr isotopes at 50.054 and 50.069/cm were obtained with a signal-to-noise ratio of 2.5. The volume mixing ratio retrieved from the average spectrum is 2.0 x 10 to the -11th, which is assumed to be constant above 28 km, with an uncertainty of 35 percent. This stratospheric amount of HBr is about the same as the current level of tropospheric organic bromine compounds, 25 pptv. Thus HBr could be the major stratospheric bromine species.
The measurement of the ClO concentration in the stratosphere provides crucial information on the mechanism for ozone depletion by catalytic reactions involving chlorine. Two rotational transitions of ClO, J = 35/2 - 33/2 and J = 37/2 - 35/2 have been identified in balloon-borne high-resolution spectra of the stratospheric emission in the submillimeter region. The measurements provide information on the ClO concentration at altitudes around 28 km. In the case of afternoon measurements obtained in April 1979, a scaling factor of 0.85 (+0.67, -0.64) is observed, and in the case of afternoon and early morning measurements obtained in October 1982, a scaling factor of 0.88 (+0.18, -0.08) is observed.
The stratospheric vertical distribution of CO is obtained from balloon-based FIR limb thermal emission spectra by analyzing several limb sequences of the R8 and R1 spectral lines at 34.588 and 49.932/cm, respectively. This constitutes the first determination of the stratospheric CO profile from IR thermal emission spectra. The results, indicating 24.6 + or - 7.6 ppbv at 21 km and 34.4 + or - 10.1 ppbv at 37 km, are compared with the remote-sensing and in situ measurements by other groups and with photochemical-dynamical model calculations.
The distribution of isotopically heavy ozone in the stratosphere has been obtained from analysis of balloon-based high-resolution thermal emission spectra in the far infrared. The mixing ratio profiles of (O-16)(O-16)(O-18) and (O-16)(O-18)(O-16), retrieved from inversion of several limb sequences of a number of spectral lines in the 39-76/cm region, indicate enhancements over the expected values in the 25- to 37-km altitude range. The ratio of total heavy isotopic ozone (10-50)3 to normal (O-48)3 shows enhancements of about 45 percent at 37 km, decreasing to a minimum of about 13 percent at 29 km, and increasing to about 18 percent at 25 km. The results from this work are compared with Mauersberger's (1987) in situ mass spectrometer measurements.
The SAFIRE (Spectroscopy of Atmospheric Far Infra-Red Emissions) experiment is discussed with particular reference to the scientific aims and the conceptual instrument design of the project. The principal requirements of the experiment are reviewed, and it is shown how these requirements are met in the instrument concept. In particular, measurements of hydrogen oxides and other important species in the stratosphere require a far infrared limb sounder. Some problems involved in the optical and thermal design of the instrument are examined.
Limb thermal emission spectra of the earth's stratosphere in the FIR obtained as part of the Balloon Intercomparison Campaign (BIC), have been analyzed for retrieval of trace constituent distributions. The observations analyzed here were made with a balloon-borne high-resolution Michelson interferometer operating in the 20-100/cm region, with an unapodized spectral resolution of 0.0033/cm. In this paper the vertical profiles of O3, H2O, and HDO retrieved from the observed spectra are presented and compared with the results from other BIC experiments. The retrieved profiles are found to be in good agreement with other measurements. The measurement of the HDO profile provides information about the sources of stratospheric water vapor. The variation of the D/H ratio of water vapor is derived from an analysis of HDO and H2O lines observed in the FIR spectra and is compared with the available measurements in the literature.
Far infrared limb thermal emission measurements of the earth's stratosphere were made with a high resolution spectrometer on a balloon payload launched from Palestine, TX, on Oct. 5, 1982. Several limb sequences of a portion of the observed spectra have been analyzed for retrieval of the stratospheric HCN profile from a number of spectral lines in the 32 to 56 cm region. The mixing ratio profile in the 20 to 37 km altitude range has been retrieved with 2-sigma uncertainties of about 4-5 km. The HCN volume mixing ratio is found to be about 139 pptv at 20 km, 127 pptv at 25 km, and increasing to 172 pptv at 37 km. The results are compared with measurements by other groups and with photochemical model calculations reported in the literature.
FIR limb thermal emission spectra obtained from balloon-borne measurements made as a part of the Balloon Intercomparison Campaign (BIC) have been analyzed for retrieval of stratospheric trace-constituent distributions. The measurements were made with a high-resolution Michelson interferometer and covered the 15-180/cm spectral range with an unapodized spectral resolution of 0.0033/cm. The retrieved vertical profiles of O3, H2O, HDO, HCN, CO, and isotopes of O3 are presented. The results are compared with the BIC measurements for O3 and H2O made from the same balloon gondola and with other published data. A comparison of the simultaneously retrieved profiles for several gases with the published data shows good agreement and indicates the validity of the FIR data and retrieval techniques and the accuracy of the inferred profiles.
An analysis method that uses the nonlinear least-squares fit technique has been developed for emission spectra obtained with a Fourier transform spectrometer. This method is used for the analysis of submillimeter-region atmospheric emission spectra obtained with a balloon-borne FT spectrometer that was carried out as a correlative measurement for the Limb IR Monitor of the Stratosphere (LIMS) satellite experiment. The retrieved mixing ratios of H2O and O3 in the stratosphere from four spectral intervals have standard deviations of about 10 percent, and the average values agree to within 10 percent of corresponding results from the LIMS satellite experiment which used a broadband emission radiometer in the IR region.
This paper discusses the spectrum of the earth's stratosphere in the far-infrared, from 5 to 250/cm. Many of the trace gases that are important in stratospheric photochemistry have been measured, or are potentially measurable in the far-infrared. The spectral features of these gases are discussed with application to spacecraft measurements. In particular, the suitability of the spectrum for measurements of the HO(x) and ClO(x) families and of O3 are compared for different classes of instruments: Fourier transform spectrometers, filter radiometers, and scanning high-resolution Fabry-Perot instruments. It is found that these types of instruments have complementary capabilities that would best be used in combination in a comprehensive multispecies measurement scheme.
Model calculations for the production of cosmic ray events in IR detectors by energy impulses due to fast charged particles' ionization trails are presently compared to the pulse-amplitude spectrum observed from a balloon at an altitude of 38 km. The results are pertinent to the current understanding of cosmic ray backgrounds found in all high sensitivity bolometer applications. The observed signal transients are in all details consistent with the modeling of known cosmic charged particle flux characteristics and with the detector response. Generally, the optics design should minimize detector/substrate cross section.
Recent progress in high-resolution measurement of sub-millimeter and far-infrared emission in the stratosphere is reviewed. Attention is given to the results of recent balloon measurements of the minor stratospheric constituents in the spectral range 40-190 per cm. Emission spectra are presented for HCl; HF; and OH. Emission spectra were also obtained for atomic oxygen; hydrobromic acid; and hydroperoxyl radical. The possibility of detecting HO2 and H2O2 in the far-infrared is also briefly discussed.