Literature DB >> 16348299

Distribution and rate of methane oxidation in sediments of the Florida everglades.

G M King1, P Roslev, H Skovgaard.   

Abstract

Rates of methane emission from intact cores were measured during anoxic dark and oxic light and dark incubations. Rates of methane oxidation were calculated on the basis of oxic incubations by using the anoxic emissions as an estimate of the maximum potential flux. This technique indicated that methane oxidation consumed up to 91% of the maximum potential flux in peat sediments but that oxidation was negligible in marl sediments. Oxygen microprofiles determined for intact cores were comparable to profiles measured in situ. Thus, the laboratory incubations appeared to provide a reasonable approximation of in situ activities. This was further supported by the agreement between measured methane fluxes and fluxes predicted on the basis of methane profiles determined by in situ sampling of pore water. Methane emissions from peat sediments, oxygen concentrations and penetration depths, and methane concentration profiles were all sensitive to light-dark shifts as determined by a combination of field and laboratory analyses. Methane emissions were lower and oxygen concentrations and penetration depths were higher under illuminated than under dark conditions; the profiles of methane concentration changed in correspondence to the changes in oxygen profiles, but the estimated flux of methane into the oxic zone changed negligibly. Sediment-free, root-associated methane oxidation showed a pattern similar to that for methane oxidation in the core analyses: no oxidation was detected for roots growing in marl sediment, even for roots of Cladium jamaicense, which had the highest activity for samples from peat sediments. The magnitude of the root-associated oxidation rates indicated that belowground plant surfaces may not markedly increase the total capacity for methane consumption. However, the data collectively support the notion that the distribution and activity of methane oxidation have a major impact on the magnitude of atmospheric fluxes from the Everglades.

Entities:  

Year:  1990        PMID: 16348299      PMCID: PMC184862          DOI: 10.1128/aem.56.9.2902-2911.1990

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  5 in total

1.  Colorless Sulfur Bacteria, Beggiatoa spp. and Thiovulum spp., in O(2) and H(2)S Microgradients.

Authors:  B B Jørgensen; N P Revsbech
Journal:  Appl Environ Microbiol       Date:  1983-04       Impact factor: 4.792

2.  Denitrification in marl and peat sediments in the Florida everglades.

Authors:  A S Gordon; W J Cooper; D J Scheidt
Journal:  Appl Environ Microbiol       Date:  1986-11       Impact factor: 4.792

Review 3.  Methane-oxidizing microorganisms.

Authors:  I J Higgins; D J Best; R C Hammond; D Scott
Journal:  Microbiol Rev       Date:  1981-12

4.  Carbon-14 in methane sources and in atmospheric methane: the contribution from fossil carbon.

Authors:  M Wahlen; N Tanaka; R Henry; B Deck; J Zeglen; J S Vogel; J Southon; A Shemesh; R Fairbanks; W Broecker
Journal:  Science       Date:  1989-07-21       Impact factor: 47.728

5.  Methane efflux from lake sediments through water lilies.

Authors:  J W Dacey; M J Klug
Journal:  Science       Date:  1979-03-23       Impact factor: 47.728

  5 in total
  18 in total

1.  Survival and Recovery of Methanotrophic Bacteria Starved under Oxic and Anoxic Conditions.

Authors:  P Roslev; G M King
Journal:  Appl Environ Microbiol       Date:  1994-07       Impact factor: 4.792

2.  Microbial Community and Greenhouse Gas Fluxes from Abandoned Rice Paddies with Different Vegetation.

Authors:  Sunghyun Kim; Seunghoon Lee; Melissa McCormick; Jae Geun Kim; Hojeong Kang
Journal:  Microb Ecol       Date:  2016-06-28       Impact factor: 4.552

3.  Use of an oxygen-insensitive microscale biosensor for methane to measure methane concentration profiles in a rice paddy.

Authors:  L R Damgaard; N P Revsbech; W Reichardt
Journal:  Appl Environ Microbiol       Date:  1998-03       Impact factor: 4.792

Review 4.  Methanotrophic bacteria.

Authors:  R S Hanson; T E Hanson
Journal:  Microbiol Rev       Date:  1996-06

5.  Regulation of root-associated methanotrophy by oxygen availability in the rhizosphere of two aquatic macrophytes.

Authors:  A Calhoun; G M King
Journal:  Appl Environ Microbiol       Date:  1997-08       Impact factor: 4.792

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

Authors:  G M King
Journal:  Appl Environ Microbiol       Date:  1996-12       Impact factor: 4.792

7.  Aerobic and anaerobic starvation metabolism in methanotrophic bacteria.

Authors:  P Roslev; G M King
Journal:  Appl Environ Microbiol       Date:  1995-04       Impact factor: 4.792

8.  Capacity for methane oxidation in landfill cover soils measured in laboratory-scale soil microcosms.

Authors:  D Kightley; D B Nedwell; M Cooper
Journal:  Appl Environ Microbiol       Date:  1995-02       Impact factor: 4.792

9.  Activity and Distribution of Methane-Oxidizing Bacteria in Flooded Rice Soil Microcosms and in Rice Plants (Oryza sativa).

Authors:  U Bosse; P Frenzel
Journal:  Appl Environ Microbiol       Date:  1997-04       Impact factor: 4.792

10.  Methane oxidation by methanotrophs and its effects on the phosphate flux over the sediment-water interface in a eutrophic lake.

Authors:  A J Sinke; F H Cottaar; K Buis; P Keizer
Journal:  Microb Ecol       Date:  1992-11       Impact factor: 4.552

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