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Detection of water vapour absorption around 363 nm in measured atmospheric absorption spectra and its effect on DOAS evaluations

MPG-Autoren
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Lampel,  J.
Satellite Remote Sensing, Max Planck Institute for Chemistry, Max Planck Society;

/persons/resource/persons140374

Wang,  Y.
Satellite Remote Sensing, Max Planck Institute for Chemistry, Max Planck Society;

/persons/resource/persons100850

Beirle,  S.
Satellite Remote Sensing, Max Planck Institute for Chemistry, Max Planck Society;

/persons/resource/persons101349

Wagner,  T.
Satellite Remote Sensing, Max Planck Institute for Chemistry, Max Planck Society;

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Zitation

Lampel, J., Pöhler, D., Polyansky, O. L., Kyuberis, A. A., Zobov, N. F., Tennyson, J., et al. (2016). Detection of water vapour absorption around 363 nm in measured atmospheric absorption spectra and its effect on DOAS evaluations. Atmospheric Chemistry and Physics Discussions, 16.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-002C-EB4E-8
Zusammenfassung
Water vapour is known to absorb radiation from the microwave region to the blue part of the visible spectrum with decreasing efficiency. Ab initio approaches to model individual absorption lines of the gaseous water molecule predict absorption lines up to its dissociation limit at 243 nm. We present the first evidence of water vapour absorption near 363 nm from field measurements using data from multi-axis differential optical absorption spectroscopy (MAX-DOAS) and long-path (LP)-DOAS measurements. The identification of the absorptions was based on the recent “POKAZATEL” line list by Polyansky et al. (2017). For MAX-DOAS measurements, we observed absorption by water vapour in an absorption band around 363 nm with optical depths of up to 2×10−3. The retrieved column densities from 2 months of measurement data and more than 2000 individual observations at different latitudes correlate well with simultaneously measured well-established water vapour absorptions in the blue spectral range from 452 to 499 nm (R2=0.89), but the line intensities at around 363 nm are underestimated by a factor of 2.6 ±0.5 by the ab initio model. At a spectral resolution of 0.5 nm, we derive a maximum cross section value of 2.7×10−27cm2 molec−1at 362.3 nm. The results were independent of the used literature absorp- tion cross section of the O4absorption, which overlays this water vapour absorption band. Also water vapour absorption around 376 nm was identi- fied. Below 360 nm no water vapour absorption above 1.4×10−26cm2 molec−1 was observed. The newly found absorption can have a significant impact on the spectral retrievals of absorbing trace-gas species in the spectral range around 363 nm. Its effect on the spectral analysis of O4 , HONO and OClO is discussed.