Dc. Lowe et al., CONCENTRATION AND C-13 RECORDS OF ATMOSPHERIC METHANE IN NEW-ZEALAND AND ANTARCTICA - EVIDENCE FOR CHANGES IN METHANE SOURCES, JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 99(D8), 1994, pp. 16913-16925
Measurements of C-13 in atmospheric methane made at Baring Head, New Z
ealand (41-degrees-S), over the 4-year period, 1989-1993, display a pe
rsistent but highly variable seasonal cycle. Values for deltaC-13 peak
in summer at about -46.9 parts per thousand and drop to around -47.5
parts per thousand in the late winter. Methane concentration shows a s
imilar cycle, with winter peaks and summer minima. Similar features ar
e observed at the New Zealand Antarctic station, Scott Base, at 78-deg
rees-S. While the phase of the deltaC-13 cycle is consistent with a ki
netic isotope effect that preferentially leaves methane enriched in C-
13 in the atmosphere after oxidation by OH, the amplitude of the cycle
is much larger than expected from published laboratory measurements o
f the effect. We interpret the origin of this cycle and its interannua
l variability to be due to episodic southward transport of isotopicall
y heavy methane from large-scale tropical biomass burning, possibly in
conjunction with changes in the rate of interhemispheric transport in
the troposphere. The Baring Head C-13 data show no significant secula
r trend from 1989 to mid-1991, followed by a rapid trend toward methan
e less enriched in C-13. This indicates a major shift in the balance o
f the sources of atmospheric methane and precludes an increased sink s
trength. The trend in C-13 since mid-1991 coincided with significant c
hanges to the methane growth rate observed at Baring Head and at Scott
Base: an elevated growth rate of about 15 parts per billion by volume
(ppbv) during 1991 gave way to less than 3 ppbv yr-1 thereafter. A 2-
box model of atmospheric methane (one box per hemispheric reservoir) s
uggests that (1) the recent decline in C-13 in methane observed at Bar
ing Head and Scott Base cannot have a solely northern hemispheric orig
in and (2) the most plausible origin is a recent reduction in methane
released by biomass burning in the southern hemisphere, combined with
a lower release rate of fossil methane in the northern hemisphere.