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Evaluating global emission inventories of biogenic bromocarbons.

Authors :
Hossaini, R.
Mantle, H.
Chipperfield, M. P.
Montzka, S. A.
Hamer, P.
Ziska, F.
Quack, B.
Krüger, K.
Tegtmeier, S.
Atlas, E.
Sala, S.
Engel, A.
Bönisch, H.
Keber, T.
Oram, D.
Mills, G.
Ordóñez, C.
Saiz-Lopez, A.
Warwick, N.
Liang, Q.
Source :
Atmospheric Chemistry & Physics; 2013, Vol. 13 Issue 23, p11819-11838, 20p, 8 Charts, 8 Graphs, 5 Maps
Publication Year :
2013

Abstract

Emissions of halogenated very short-lived substances (VSLS) are poorly constrained. However, their inclusion in global models is required to simulate a realistic inorganic bromine (Br<subscript>y</subscript>) loading in both the troposphere, where bromine chemistry perturbs global oxidizing capacity, and in the stratosphere, where it is a major sink for ozone (O<subscript>3</subscript>). We have performed simulations using a 3-D chemical transport model (CTM) including three top-down and a single bottom-up derived emission inventory of the major brominated VSLS bromoform (CHBr<subscript>3</subscript>) and dibromomethane (CH<subscript>2</subscript>Br<subscript>2</subscript>). We perform the first concerted evaluation of these inventories, comparing both the magnitude and spatial distribution of emissions. For a quantitative evaluation of each inventory, model output is compared with independent long-term observations at National Oceanic and Atmospheric Administration (NOAA) ground-based stations and with aircraft observations made during the NSF HIAPER Pole-to-Pole Observations (HIPPO) project. For CHBr<subscript>3</subscript>, the mean absolute deviation between model and surface observation ranges from 0.22 (38%) to 0.78 (115%) parts per trillion (ppt) in the tropics, depending on emission inventory. For CH<subscript>2</subscript>Br<subscript>2</subscript>, the range is 0.17 (24%) to 1.25 (167%) ppt. We also use aircraft observations made during the 2011 "Stratospheric Ozone: Halogen Impacts in a Varying Atmosphere" (SHIVA) campaign, in the tropical West Pacific. Here, the performance of the various inventories also varies significantly, but overall the CTM is able to reproduce observed CHBr<subscript>3</subscript> well in the free troposphere using an inventory based on observed sea-to-air fluxes. Finally, we identify the range of uncertainty associated with these VSLS emission inventories on stratospheric bromine loading due to VSLS (Br<subscript>y</subscript>VSLS). Our simulations show Br<subscript>y</subscript>VSLS ranges from ~ 4.0 to 8.0 ppt depending on the inventory. We report an optimised estimate at the lower end of this range (~ 4 ppt) based on combining the CHBr<subscript>3</subscript> and CH<subscript>2</subscript>Br<subscript>2</subscript> inventories which give best agreement with the compilation of observations in the tropics. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16807316
Volume :
13
Issue :
23
Database :
Complementary Index
Journal :
Atmospheric Chemistry & Physics
Publication Type :
Academic Journal
Accession number :
92997133
Full Text :
https://doi.org/10.5194/acp-13-11819-2013