[1] The High Resolution Dynamics Limb Sounder (HIRDLS) experiment was designed to provide global temperature and composition data on the region from the upper troposphere to the mesopause with vertical and horizontal resolution not previously available. The science objectives are the study of small-scale dynamics and transports, including stratosphere-troposphere exchange, upper troposphere/lower stratosphere chemistry, aerosol, cirrus and PSC distributions, and gravity waves. The instrument features 21 channels, low noise levels, high vertical resolution, and a mechanical cooler for long life. During launch most of the optical aperture became obscured, so that only a potion of an optical beam width at a large azimuth from the orbital plane on the side away from the Sun can see the atmosphere. Irrecoverable loss of capabilities include limitation of coverage to the region 65°S-82°N and inability to obtain longitudinal resolution finer than an orbital spacing. While this optical blockage also impacted radiometric performance, extensive effort has gone into developing corrections for the several effects of the obstruction, so that radiances from some of the channels can be put into retrievals for temperature. Changes were also necessary for the retrieval algorithm. The validation of the resulting temperature retrievals is presented to demonstrate the effectiveness of these corrections. The random errors range from $0.5 K at 20 km to $1.0 at 60 km, close to those predicted. Comparisons with high-resolution radiosondes, lidars, ACE-FTS, and ECMWF analyses give a consistent picture of HIRDLS temperatures being 1-2 K warm from 200 to 10 hPa and within ±2 K of standards from 200 to 2 hPa (but warmer in the region of the tropical tropopause), above which HIRDLS appears to be cold. Comparisons show that both COSMIC and HIRDLS can see small vertical features down to about 2 km

We have used a high resolution infrared spectrometer aboard the NASA Wallops Flight Facility Electra aircraft to measure the total column amount of SO2, O3, and HCl above the aircraft while flying over the Caribbean three weeks after the June 15 eruption of Mt. Pinatubo in the Philippines, South of 20°N latitude we observed columns of SO2 ranging from 2.0 × 1016 to 3.7 × 1016 molecules‐cm−2. In addition, the column amount of HCl averaged 1.5 × 1015 molecules‐cm−2 in the region of the plume. This may represent a small increase in HCl above the amount, estimated from our previous measurements, that would have been present had there been no volcanic eruption, but the increase is substantially less than that seen following the 1982 eruptions of El Chichón [Mankin and Coffey, 1984].

Spectroscopic observations of the total column amount of hydrogen chloride above an altitude of 12 kilometers in the latitude range 20 degrees to 40 degrees N have been made both before and 3 to 6 months after the eruptions of El Chichón Volcano in March and April 1982. In the region of the cloud of volcanic aerosols, the hydrogen chloride total column after the eruptions increased by approximately 40 percent, even after allowance is made for the global secular increase in hydrogen chloride of 5 percent per year. The column amounts of hydrogen fluoride show no such increase.

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Abstract. An intercomparison of four Fourier transform infrared (FTIR) spectrometers, operated side by side by Jet Propulsion Laboratory (JPL), National Center for Atmospheric Research, and National Physical Laboratory groups, using two different spectral fitting algorithms, was conducted at JPL's Table Mountain Facility (TMF) during November 1996. A "blind" comparison of retrieved vertical column amounts, of preselected trace gases in preselected microwindows (mw), and subsequent reanalysis of the results are described. The species analyzed are N2 (3 mw), HF (1 mw), HC1 (1 mw), CH4 (1 mw), 03 (2 mw), N20 (2 mw), HNO3 (2 mw), and CO2 (1 mw). The column agreements from the "blind" phase were within 0.5-2%, except that for HNO3, HF, and 03 the disagreement of the results was up to 10%, 5%, and 4%, respectively. It was found that several systematic effects were neglected in the "blind" phase analysis. Taking these into account in the postanalysis reduced the disagreements to 0.5-1.0% for most cases, and to less than 4%, 3%, and 1% for HNO3, HF, and 03 respectively. It was concluded that zero offsets caused by detector nonlinearity were the main cause of the large errors in HNO3 and other gases (i.e., CO2) retrieved from the HgCdTe spectra. At shorter wavelengths (i.e., HF) we conclude that incomplete modeling of the instrument line shapes (ILS) was the main cause of column differences larger than 1%.