EGU2020-1008
https://doi.org/10.5194/egusphere-egu2020-1008
EGU General Assembly 2020
© Author(s) 2020. This work is distributed under
the Creative Commons Attribution 4.0 License.

A novel technique for studying volcanic gas chemistry and dispersion on short time scales

Christopher Fuchs1, Jonas Kuhn1,2, Nicole Bobrowski1,2, and Ulrich Platt1,2
Christopher Fuchs et al.
  • 1Institute of Environmental Physics, University of Heidelberg, Germany, (cfuchs@iup.uni-heidelberg.de)
  • 2Max Planck Institute for Chemistry, Mainz, Germany

Volcanic gas emissions, in particular, of sulphur and halogen species, play an important role in atmospheric chemistry. Due to the complex reaction kinetics of halogen radicals inside the volcanic plume, many properties like e.g. chemistry limiting factors and timescales of reactions, are still not well understood.
Imaging techniques based on optical remote sensing can get valuable insights into the study of both volcanic degassing fluxes and chemical conversions within the plume that continuously mixes with the atmosphere. However, state-of-the-art techniques are either too slow to resolve plume chemistry processes on its intrinsic time scales (e.g. DOAS) or show many cross sensitivities and hence are limited to rather high trace gas concentrations (e.g. SO2 cameras). 

We introduce a novel technique for volcanic trace gas imaging, which, by employing a Fabry-Perot interferometer (FPI), uses detailed spectral information for the detection of the target trace gas. Cross sensitivities are thereby drastically reduced, allowing for the detection of much lower SO2 concentrations and imaging of other trace gas species like, e.g., BrO, OClO. Furthermore, the inherent calibration of the new techniques avoids the requirement of additional DOAS measurements or gas cells for calibration.

We present the first measurements of volcanic SO2 with an imaging Fabry-Perot interferometer correlation spectroscopy (IFPICS) prototype. The sensitivity of ≈ 1019 cm2 molec-1 is comparable to filter based SO2 cameras, whereas the selectivity is much higher (e.g. no ozone interference). This will largely increase the accuracy of SO2 emission rates, which are routinely used to approximate fluxes of other volcanic gas emissions into the atmosphere.

Additionally, sensitivity studies for further trace gases combining laboratory measurements and radiation transfer modelling show promising prospected BrO detection limits of < 1014 molec cm-², corresponding to mixing ratios of 10 to 100 ppt in volcanic plumes. The direct visualisation of BrO within the volcanic plume mixing with the ambient atmosphere will give important insights into the plume’s halogen chemistry and, thereby, its impact on the atmosphere.

How to cite: Fuchs, C., Kuhn, J., Bobrowski, N., and Platt, U.: A novel technique for studying volcanic gas chemistry and dispersion on short time scales, EGU General Assembly 2020, Online, 4–8 May 2020, EGU2020-1008, https://doi.org/10.5194/egusphere-egu2020-1008, 2019

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