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Appl. Environ. Microbiol., Dec 1996, 4548-4555, Vol 62, No. 12
GM King
Methane oxidation associated with the belowground tissues of a common
aquatic macrophyte, the burweed Sparganium eurycarpum, was assayed in situ
by a chamber technique with acetylene or methyl fluoride as a
methanotrophic inhibitor at a headspace concentration of 3 to 4%. Acetylene
and methyl fluoride inhibited both methane oxidation and peat
methanogenesis. However, inhibition of methanogenesis resulted in no
obvious short-term effect on methane fluxes. Since neither inhibitor
adversely affected plant metabolism and both inhibited methanotrophy
equally well, acetylene was employed for routine assays because of its low
cost and ease of use. Root-associated methanotrophy consumed a variable but
significant fraction of the total potential methane flux; values varied
between 1 and 58% (mean (plusmn) standard deviation, 27.0% (plusmn) 6.0%)
with no consistent temporal or spatial pattern during late summer. The
absolute amount of methane oxidized was not correlated with the total
potential methane flux; this suggested that parameters other than methane
availability (e.g., oxygen availability) controlled the rates of methane
oxidation. Estimates of diffusive methane flux and oxidation at the peat
surface indicated that methane emission occurred primarily through
aboveground plant tissues; the absolute magnitude of methane oxidation was
also greater in association with roots than at the peat surface. However,
the relative extent of oxidation was greater at the latter locus.
Copyright © 1996, American Society for Microbiology
In Situ Analyses of Methane Oxidation Associated with the Roots and Rhizomes of a Bur Reed, Sparganium eurycarpum, in a Maine Wetland
Darling Marine Center, University of Maine, Walpole, Maine 04573
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