Diurnal variability and night detection of stratospheric hydroxyl radical from far infrared emission measurements

Citation
M. Carlotti et al., Diurnal variability and night detection of stratospheric hydroxyl radical from far infrared emission measurements, J ATMOS S-P, 63(14), 2001, pp. 1509-1518
Citations number
24
Categorie Soggetti
Earth Sciences
Journal title
JOURNAL OF ATMOSPHERIC AND SOLAR-TERRESTRIAL PHYSICS
ISSN journal
13646826 → ACNP
Volume
63
Issue
14
Year of publication
2001
Pages
1509 - 1518
Database
ISI
SICI code
1364-6826(200109)63:14<1509:DVANDO>2.0.ZU;2-E
Abstract
We report the measurement of the stratospheric hydroxyl radical (OH) perfor med with a balloon-borne far-infrared Fourier Transform Spectrometer. Conti nuous observations were made, on a mid-latitude air mass, between 15 km and about 38 km, with a cycling limb-scanning observation technique. The measu rement period commenced before the local noon and ended just before sunrise on the following day, permitting nearly complete observations of the diurn al OH cycle. A retrieval analysis of the daytime observations has produced a set of altitude-distribution profiles of the volume-mixing ratio, from 22 to 38 km, that provides a picture of the variation of the radical as a fun ction of the solar zenith angle at 1 km altitude steps. Above 38 km column density values have been determined. The observations taken at sunset show the expected rapid decay of OH. The nighttime data also show residual spect ral features in correspondence to OH transitions. A spectroscopic analysis, carried out with the help of simulated spectra, indicates that these spect ral features are most likely due to the OH transitions and hence these data provide the first positive detection of OH in the stratosphere in darkness . The retrieval analysis of the nighttime spectral features has established that the nighttime OH distribution is peaked around 36 km with a mixing ra tio of 3.2 +/- 2.0 ppt; values for the column density are also determined a bove and below this altitude. (C) 2001 Elsevier Science Ltd. All rights res erved.