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Introduction:
The bromine monoxide radical (BrO) is well known for its role in
stratospheric ozone destruction, in particular in combination with ClO. In
contrast to chlorine, bromine is in its active forms in the sunlit stratosphere
and BrO is one of the dominant bromine species during daytime. While overall the
contribution of bromine to stratospheric ozone loss is smaller than that of
chlorine as result of its lower abundance, emission of source gases is not yet
declining as is the case for chlorine. Thus, the relative role of bromine could
still be increasing.
Large concentrations of BrO are also observed in the polar boundary layer in
spring time during so called ozone depletion events when ozone levels close to
the surface are strongly reduced. This bromine originates from sea salt and is
released to the gas phase through heterogeneous processes on ice or snow the
details of which are not yet fully understood. One hypothesis is that
concentrated brine on frost flowers acts as the source either directly or once
the frost flowers disintegrate into wind blown aerosol. Once bromine is released
to the gas phase, BrO is formed and can be amplified through an autocatalytic
release from aerosols leading to "bromine explosions" with rapid ozone loss. An
example of typical BrO fields during polar spring are given in the figure above.
Please refer to the data section for a discussion of issues
related to BrO retrieval from satellite.
From ground-based DOAS measurements, comparison of satellite and ground-based
measurements and also from balloon-borne measurements there is indication for
the presence of a BrO background of about 1ppt in the free troposphere. The
source of this BrO could be either short lived organic compounds, transport of
air affected by polar bromine explosions or volcanic eruptions. In the absence
of direct measurements, this tropospheric background is still under debate.
Multi-axis DOAS measurements near active volcanoes provide evidence for very
large BrO concentrations in some volcanic plumes. The signal has been observed
at several different volcanoes, albeit at different levels relative to SO2
concentrations. No BrO could be observed in GOME and SCIAMACHY measurements
during large volcanic eruptions, indicating that under these conditions BrO
emissions are much smaller than during degassing.
Data:
Images of daily, monthly, and annual averages of BrO can be viewed on our
SCIAMACHY data browser
page. Data files are available from
Andreas Richter
on request.
When using satellite retrieved BrO columns, one as to keep in mind that
measurements in the UV/visible spectral range do not provide vertical resolution
for BrO. Thus, it can not easily be decided which part of the signal originates
from the boundary layer, the free troposphere or the stratosphere.
Unfortunately, the sensitivity of the measurements to BrO varies with altitude
as a function of surface reflectivity (this is illustrated in our interactive
airmass factor calculator). Proper analysis of the measurements therefore
requires an assumption on the vertical distribution of the BrO (e.g. from model
calculations) and knowledge of surface albedo and cloud cover, cloud top
altitude, and cloud optical depth. While we a re currently working on such a
detailed retrieval using nadir measurements in combination with SCIAMACHY limb
profiles, the data shown on this page and in the data browser are calculated
assuming a stratospheric profile. They quite accurate for regions where the
stratosphere and upper troposphere dominates, underestimate the total column
over dark surfaces if significant BrO amounts are present in the troposphere and
overestimate the total column over bright surfaces if BrO is present in the
lower atmosphere.
An additional complication arises for SCIAMACHY data from an instrumental
feature in the spectral region traditionally used for the BrO retrieval (345 -
359 nm). To avoid the large noise resulting from this feature, the BrO retrieval
for SCIAMACHY is performed in the 336 - 347 nm region where a low bias in BrO is
observed in the presence of large HCHO signals, e.g. over rain forests or during
large biomass burning.
A short description of the algorithm used for the BrO data product can be
found in the BrO Algorithm
Description.
References:
-
Jacobi, H., L. Kaleschke, A. Richter, A. Rozanov, and J. P. Burrows,
Observation of a fast ozone loss in the
marginal ice zone of the Arctic Ocean, J. Geophys. Res., 111,
D15309, doi:10.1029/2005JD006715, 2006
-
Sinnhuber,
B.-M., Rozanov, A., Sheode, N., Afe, O. T., Richter, A., Sinnhuber, M., Wittrock,
F., Burrows, J. P., Global observations of
stratospheric bromine monoxide from SCIAMACHY, Geophys. Res. Lett.,
32, L20810, doi:10.1029/2005GL023839, 2005.
- Afe, O. T., A. Richter, B. Sierk, F. Wittrock and J. P. Burrows,
BrO Emission from Volcanoes - a
Survey using GOME and SCIAMACHY Measurements, Geophys. Res.Lett.,
31, L24113, doi:10.1029/2004GL020994, 2004
Contact:
If you are interested in more information or SCIAMACHY BrO data, please contact
Andreas Richter.
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