Bromoform and dibromomethane in the tropics: a 3-D model study of chemistry and transport

We have developed a detailed chemical scheme for the degradation of the short-lived source gases bromoform (CHBr<sub>3</sub>) and dibromomethane (CH<sub>2</sub>Br<sub>2</sub>) and implemented it in the TOMCAT/SLIMCAT...

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Main Authors: R. Hossaini, M. P. Chipperfield, B. M. Monge-Sanz, N. A. D. Richards, E. Atlas, D. R. Blake
Format: Article
Language:English
Published: Copernicus Publications 2010-01-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/10/719/2010/acp-10-719-2010.pdf
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spelling doaj-c0b25d3d4a7043a69488a7677cfd54f12020-11-24T22:48:05ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242010-01-01102719735Bromoform and dibromomethane in the tropics: a 3-D model study of chemistry and transportR. HossainiM. P. ChipperfieldB. M. Monge-SanzN. A. D. RichardsE. AtlasD. R. BlakeWe have developed a detailed chemical scheme for the degradation of the short-lived source gases bromoform (CHBr<sub>3</sub>) and dibromomethane (CH<sub>2</sub>Br<sub>2</sub>) and implemented it in the TOMCAT/SLIMCAT three-dimensional (3-D) chemical transport model (CTM). The CTM has been used to predict the distribution of the two source gases (SGs) and 11 of their organic product gases (PGs). These first global calculations of the organic PGs show that their abundance is small. The longest lived organic PGs are CBr<sub>2</sub>O and CHBrO, but their peak tropospheric abundance relative to the surface volume mixing ratio (vmr) of the SGs is less than 5%. We calculate their mean local tropospheric lifetimes in the tropics to be ~7 and ~2 days (due to photolysis), respectively. Therefore, the assumption in previous modelling studies that SG degradation leads immediately to inorganic bromine seems reasonable. <br><br> We have compared observed tropical SG profiles from a number of aircraft campaigns with various model experiments. In the tropical tropopause layer (TTL) we find that the CTM run using p levels (TOMCAT) and vertical winds from analysed divergence overestimates the abundance of CH<sub>2</sub>Br<sub>2</sub>, and to a lesser extent CHBr<sub>3</sub>, although the data is sparse and comparisons are not conclusive. Better agreement in the TTL is obtained in the sensitivity run using θ levels (SLIMCAT) and vertical motion from diabatic heating rates. Trajectory estimates of residence times in the two model versions show slower vertical transport in the SLIMCAT θ-level version. In the p-level model even when we switch off convection we still find significant amounts of the SGs considered may reach the cold point tropopause; the stratospheric source gas injection (SGI) is only reduced by ~16% for CHBr<sub>3</sub> and ~2% for CH<sub>2</sub>Br<sub>2</sub> without convection. <br><br> Overall, the relative importance of the SG pathway and the PG pathway for transport of bromine to the stratospheric overworld (θ>380 K) has been assessed. Assuming a 10-day washout lifetime of Br<sub>y</sub> in TOMCAT, we find the delivery of total Br from CHBr<sub>3</sub> to be 0.72 pptv with ~53% of this coming from SGI. Similary, for CH<sub>2</sub>Br<sub>2</sub> we find a total Br value of 1.69 pptv with ~94% coming from SGI. We infer that these species contribute ~2.4 pptv of inorganic bromine to the lower stratosphere with SGI being the dominant pathway. Slower transport to and through the TTL would decrease this estimate. http://www.atmos-chem-phys.net/10/719/2010/acp-10-719-2010.pdf
collection DOAJ
language English
format Article
sources DOAJ
author R. Hossaini
M. P. Chipperfield
B. M. Monge-Sanz
N. A. D. Richards
E. Atlas
D. R. Blake
spellingShingle R. Hossaini
M. P. Chipperfield
B. M. Monge-Sanz
N. A. D. Richards
E. Atlas
D. R. Blake
Bromoform and dibromomethane in the tropics: a 3-D model study of chemistry and transport
Atmospheric Chemistry and Physics
author_facet R. Hossaini
M. P. Chipperfield
B. M. Monge-Sanz
N. A. D. Richards
E. Atlas
D. R. Blake
author_sort R. Hossaini
title Bromoform and dibromomethane in the tropics: a 3-D model study of chemistry and transport
title_short Bromoform and dibromomethane in the tropics: a 3-D model study of chemistry and transport
title_full Bromoform and dibromomethane in the tropics: a 3-D model study of chemistry and transport
title_fullStr Bromoform and dibromomethane in the tropics: a 3-D model study of chemistry and transport
title_full_unstemmed Bromoform and dibromomethane in the tropics: a 3-D model study of chemistry and transport
title_sort bromoform and dibromomethane in the tropics: a 3-d model study of chemistry and transport
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2010-01-01
description We have developed a detailed chemical scheme for the degradation of the short-lived source gases bromoform (CHBr<sub>3</sub>) and dibromomethane (CH<sub>2</sub>Br<sub>2</sub>) and implemented it in the TOMCAT/SLIMCAT three-dimensional (3-D) chemical transport model (CTM). The CTM has been used to predict the distribution of the two source gases (SGs) and 11 of their organic product gases (PGs). These first global calculations of the organic PGs show that their abundance is small. The longest lived organic PGs are CBr<sub>2</sub>O and CHBrO, but their peak tropospheric abundance relative to the surface volume mixing ratio (vmr) of the SGs is less than 5%. We calculate their mean local tropospheric lifetimes in the tropics to be ~7 and ~2 days (due to photolysis), respectively. Therefore, the assumption in previous modelling studies that SG degradation leads immediately to inorganic bromine seems reasonable. <br><br> We have compared observed tropical SG profiles from a number of aircraft campaigns with various model experiments. In the tropical tropopause layer (TTL) we find that the CTM run using p levels (TOMCAT) and vertical winds from analysed divergence overestimates the abundance of CH<sub>2</sub>Br<sub>2</sub>, and to a lesser extent CHBr<sub>3</sub>, although the data is sparse and comparisons are not conclusive. Better agreement in the TTL is obtained in the sensitivity run using θ levels (SLIMCAT) and vertical motion from diabatic heating rates. Trajectory estimates of residence times in the two model versions show slower vertical transport in the SLIMCAT θ-level version. In the p-level model even when we switch off convection we still find significant amounts of the SGs considered may reach the cold point tropopause; the stratospheric source gas injection (SGI) is only reduced by ~16% for CHBr<sub>3</sub> and ~2% for CH<sub>2</sub>Br<sub>2</sub> without convection. <br><br> Overall, the relative importance of the SG pathway and the PG pathway for transport of bromine to the stratospheric overworld (θ>380 K) has been assessed. Assuming a 10-day washout lifetime of Br<sub>y</sub> in TOMCAT, we find the delivery of total Br from CHBr<sub>3</sub> to be 0.72 pptv with ~53% of this coming from SGI. Similary, for CH<sub>2</sub>Br<sub>2</sub> we find a total Br value of 1.69 pptv with ~94% coming from SGI. We infer that these species contribute ~2.4 pptv of inorganic bromine to the lower stratosphere with SGI being the dominant pathway. Slower transport to and through the TTL would decrease this estimate.
url http://www.atmos-chem-phys.net/10/719/2010/acp-10-719-2010.pdf
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