LOGIN TO YOUR ACCOUNT

Username
Password
Remember Me
Or use your Academic/Social account:

CREATE AN ACCOUNT

Or use your Academic/Social account:

Congratulations!

You have just completed your registration at OpenAire.

Before you can login to the site, you will need to activate your account. An e-mail will be sent to you with the proper instructions.

Important!

Please note that this site is currently undergoing Beta testing.
Any new content you create is not guaranteed to be present to the final version of the site upon release.

Thank you for your patience,
OpenAire Dev Team.

Close This Message

CREATE AN ACCOUNT

Name:
Username:
Password:
Verify Password:
E-mail:
Verify E-mail:
*All Fields Are Required.
Please Verify You Are Human:
fbtwitterlinkedinvimeoflicker grey 14rssslideshare1
Butler, Robyn; Palmer, Paul I.; Feng, Liang; Andrews, Stephen J.; Atlas, Elliot L.; Carpenter, Lucy J.; Donets, Valeria; Harris, Neil R. P.; Montzka, Stephen A.; Pan, Laura L.; Salawitch, Ross J.; Schauffler, Sue M. (2016)
Languages: English
Types: Article
Subjects:
We use the GEOS-Chem global 3-D atmospheric chemistry transport model to interpret atmospheric observations of bromoform (CHBr3) and dibromomethane (CH2Br2) collected during the CAST and CONTRAST aircraft measurement campaigns over the Western Pacific, January–February, 2014. We use a new linearised, tagged version of CHBr3 and CH2Br2, allowing us to study the influence of emissions from specific geographical regions on observed atmospheric variations. The model describes 32 %–37 % of CHBr3 observed variability and 15 %–45 % of CH2Br2 observed variability during CAST and CONTRAST, reflecting errors in vertical model transport. The model has a mean positive bias of 30 % that is larger near the surface reflecting errors in the poorly constrained prior emission estimates. We find using the model that observed variability of CHBr3 and CH2Br2 is driven by ocean emissions, particularly by the open ocean above which there is deep convection. We find that contributions from coastal oceans and terrestrial sources over the Western Pacific are significant above altitudes > 6 km, but is still dominated by the open ocean emissions and by air masses transported over longer time lines than the campaign period. In the absence of reliable ocean emission estimates, we use a new physical age of air simulation to determine the relative abundance of halogens delivered by CHBr3 and CH2Br2 to the tropical transition layer (TTL). We find that 6 % (47 %) of air masses with halogen released by the ocean reach the TTL within two (three) atmospheric e-folding lifetimes of CHBr3 and almost all of them reach the TTL within one e-folding lifetime of CH2Br2. We find these gases are delivered to the TTL by a small number of rapid convection events during the study period. Over the duration of CAST and CONTRAST and over our study region, oceans delivered a mean (range) CHBr3 and CH2Br2 mole fraction of 0.46 (0.13–0.72) and 0.88 (0.71–1.01) pptv, respectively, to the TTL, and a mean (range) Bry mole fraction of 3.14 (1.81–4.18) pptv to the upper troposphere. Open ocean emissions are responsible for 75 % of these values, with only 8 % from coastal oceans.

Share - Bookmark

Cite this article

Collected from