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Nitrous oxide and methane in the Atlantic Ocean between 50˚N and 52˚S: latitudinal distribution and sea-to-air flux
Lookup NU author(s)
Grant Forster
Professor Robert Upstill-Goddard
Dr Guenther Uher
Author(s)
Forster GL, Upstill-Goddard RC, Gist N, Robinson R, Uher G, Woodward EMS
Publication type
Article
Journal
Deep Sea Research II: Topical Studies in Oceanography
Year
2009
Volume
56
Issue
15
Pages
964-976
ISSN (print)
0967-0645
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
We discuss nitrous oxide (N
2
O) and methane (CH
4
) distributions in 49 vertical profiles covering the upper 300 m of the water column along two 13,500 km transects between 50°N and 52°S during the Atlantic Meridional Transect (AMT) programme (AMT cruises 12 and 13). Vertical N
2
O profiles were amenable to analysis on the basis of common features coincident with Longhurst provinces. In contrast, CH
4
showed no such pattern. The most striking feature of the latitudinal depth distributions was a well-defined “plume” of exceptionally high N
2
O concentrations coincident with very low levels of CH
4
, located between 23.5°N and 23.5°S; this feature reflects the upwelling of deep waters containing N
2
O derived from nitrification, as identified by an analysis of N
2
O, apparent oxygen utilization (AOU) and NO
3
−
, and presumably depleted in CH
4
by bacterial oxidation. Sea-to-air emissions fluxes for a region equivalent to 42% of the Atlantic Ocean surface area were in the range 0.40–0.68 Tg N
2
O yr
−1
and 0.81–1.43 Tg CH
4
yr
−1
. Based on contemporary estimates of the global ocean source strengths of atmospheric N
2
O and CH
4
, the Atlantic Ocean could account for 6–15% and 4–13%, respectively, of these source totals. Given that the Atlantic Ocean accounts for around 20% of the global ocean surface, on unit area basis it appears that the Atlantic may be a slightly weaker source of atmospheric N
2
O than other ocean regions but it could make a somewhat larger contribution to marine-derived atmospheric CH
4
than previously thought.
Publisher
Pergamon
URL
http://dx.doi.org/10.1016/j.dsr2.2008.12.002
DOI
10.1016/j.dsr2.2008.12.002
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