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. 1996 Dec;62(12):4548–4555. doi: 10.1128/aem.62.12.4548-4555.1996

In Situ Analyses of Methane Oxidation Associated with the Roots and Rhizomes of a Bur Reed, Sparganium eurycarpum, in a Maine Wetland

G M King
PMCID: PMC1389005  PMID: 16535467

Abstract

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.

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Selected References

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  1. Dacey J. W. Internal winds in water lilies: an adaptation for life in anaerobic sediments. Science. 1980 Nov 28;210(4473):1017–1019. doi: 10.1126/science.210.4473.1017. [DOI] [PubMed] [Google Scholar]
  2. Dacey J. W., Klug M. J. Methane efflux from lake sediments through water lilies. Science. 1979 Mar 23;203(4386):1253–1255. doi: 10.1126/science.203.4386.1253. [DOI] [PubMed] [Google Scholar]
  3. King G. M. Associations of methanotrophs with the roots and rhizomes of aquatic vegetation. Appl Environ Microbiol. 1994 Sep;60(9):3220–3227. doi: 10.1128/aem.60.9.3220-3227.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. King G. M., Roslev P., Skovgaard H. Distribution and rate of methane oxidation in sediments of the Florida everglades. Appl Environ Microbiol. 1990 Sep;56(9):2902–2911. doi: 10.1128/aem.56.9.2902-2911.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Nouchi I., Mariko S., Aoki K. Mechanism of Methane Transport from the Rhizosphere to the Atmosphere through Rice Plants. Plant Physiol. 1990 Sep;94(1):59–66. doi: 10.1104/pp.94.1.59. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Oremland R. S., Culbertson C. W. Evaluation of methyl fluoride and dimethyl ether as inhibitors of aerobic methane oxidation. Appl Environ Microbiol. 1992 Sep;58(9):2983–2992. doi: 10.1128/aem.58.9.2983-2992.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Oremland R. S., Taylor B. F. Inhibition of methanogenesis in marine sediments by acetylene and ethylene: validity of the acetylene reduction assay for anaerobic microcosms. Appl Microbiol. 1975 Oct;30(4):707–709. doi: 10.1128/am.30.4.707-709.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]

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