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Microbiological processes in the terrestrial carbon cycle: Methane cycling in peat

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Microbiological processes in the terrestrial carbon cycle: Methane cycling in peat. / Edwards, C.; Hales, B. A.; Hall, G. H. et al.
In: Atmospheric Environment, Vol. 32, No. 19, 01.10.1998, p. 3247-3255.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Edwards, C, Hales, BA, Hall, GH, McDonald, IR, Murrell, JC, Pickup, R, Ritchie, DA, Saunders, JR, Simon, BM & Upton, M 1998, 'Microbiological processes in the terrestrial carbon cycle: Methane cycling in peat', Atmospheric Environment, vol. 32, no. 19, pp. 3247-3255. https://doi.org/10.1016/S1352-2310(98)00107-1

APA

Edwards, C., Hales, B. A., Hall, G. H., McDonald, I. R., Murrell, J. C., Pickup, R., Ritchie, D. A., Saunders, J. R., Simon, B. M., & Upton, M. (1998). Microbiological processes in the terrestrial carbon cycle: Methane cycling in peat. Atmospheric Environment, 32(19), 3247-3255. https://doi.org/10.1016/S1352-2310(98)00107-1

Vancouver

Edwards C, Hales BA, Hall GH, McDonald IR, Murrell JC, Pickup R et al. Microbiological processes in the terrestrial carbon cycle: Methane cycling in peat. Atmospheric Environment. 1998 Oct 1;32(19):3247-3255. doi: 10.1016/S1352-2310(98)00107-1

Author

Edwards, C. ; Hales, B. A. ; Hall, G. H. et al. / Microbiological processes in the terrestrial carbon cycle : Methane cycling in peat. In: Atmospheric Environment. 1998 ; Vol. 32, No. 19. pp. 3247-3255.

Bibtex

@article{47db9ad06b934d83b02395281abf91dc,
title = "Microbiological processes in the terrestrial carbon cycle: Methane cycling in peat",
abstract = "Coring and cutting devices were developed to extract 30 cm cores from peat under conditions which preserve their physical/spatial integrity, maintain anoxic conditions and allow transverse sectioning. Methane production potential, measured on 1-2 cm vertical sections, was broadly absent from the upper 5 cm, maximum in the next 10 cm and thereafter declined. Methane oxidation potential was maximum in the upper 10 cm and thereafter detected in reducing amounts. Molecular methods, based on the extraction of total DNA and its PCR amplification and hybridisation with specific phylogenetic 16S rRNA and functional gene specific primers and probes, were developed to analyse the methane producing and methane oxidising microbial communities. The functional gene sequences were based on methanogen methyl coenzyme reductase and methanotroph methane monooxygenase. Methanotrophs are located throughout the core whereas methanogens are restricted to the lower zones. The composition of the microbial communities is however complex consisting of a number of novel species not previously recognised and with the various species/sub-groups occupying different vertical zones.",
keywords = "Methanogens, Methanotrophs, Microbial diversity, Molecular probes, Polymerase chain reaction",
author = "C. Edwards and Hales, {B. A.} and Hall, {G. H.} and McDonald, {I. R.} and Murrell, {J. C.} and R. Pickup and Ritchie, {D. A.} and Saunders, {J. R.} and Simon, {B. M.} and M. Upton",
note = "Funding Information: We thank NERC for financial support provided through the TIGER programme (Grant Nos: GST/02/621, GST/02/622 and GST/02/623, the National Trust for access to the Moorhouse site and permision to remove samples, the Daresbury Laboratory for access to SEQNET facility for DNA sequence analysis and Angela Rosin for the DNA sequencing.",
year = "1998",
month = oct,
day = "1",
doi = "10.1016/S1352-2310(98)00107-1",
language = "English",
volume = "32",
pages = "3247--3255",
journal = "Atmospheric Environment",
issn = "1352-2310",
publisher = "PERGAMON-ELSEVIER SCIENCE LTD",
number = "19",

}

RIS

TY - JOUR

T1 - Microbiological processes in the terrestrial carbon cycle

T2 - Methane cycling in peat

AU - Edwards, C.

AU - Hales, B. A.

AU - Hall, G. H.

AU - McDonald, I. R.

AU - Murrell, J. C.

AU - Pickup, R.

AU - Ritchie, D. A.

AU - Saunders, J. R.

AU - Simon, B. M.

AU - Upton, M.

N1 - Funding Information: We thank NERC for financial support provided through the TIGER programme (Grant Nos: GST/02/621, GST/02/622 and GST/02/623, the National Trust for access to the Moorhouse site and permision to remove samples, the Daresbury Laboratory for access to SEQNET facility for DNA sequence analysis and Angela Rosin for the DNA sequencing.

PY - 1998/10/1

Y1 - 1998/10/1

N2 - Coring and cutting devices were developed to extract 30 cm cores from peat under conditions which preserve their physical/spatial integrity, maintain anoxic conditions and allow transverse sectioning. Methane production potential, measured on 1-2 cm vertical sections, was broadly absent from the upper 5 cm, maximum in the next 10 cm and thereafter declined. Methane oxidation potential was maximum in the upper 10 cm and thereafter detected in reducing amounts. Molecular methods, based on the extraction of total DNA and its PCR amplification and hybridisation with specific phylogenetic 16S rRNA and functional gene specific primers and probes, were developed to analyse the methane producing and methane oxidising microbial communities. The functional gene sequences were based on methanogen methyl coenzyme reductase and methanotroph methane monooxygenase. Methanotrophs are located throughout the core whereas methanogens are restricted to the lower zones. The composition of the microbial communities is however complex consisting of a number of novel species not previously recognised and with the various species/sub-groups occupying different vertical zones.

AB - Coring and cutting devices were developed to extract 30 cm cores from peat under conditions which preserve their physical/spatial integrity, maintain anoxic conditions and allow transverse sectioning. Methane production potential, measured on 1-2 cm vertical sections, was broadly absent from the upper 5 cm, maximum in the next 10 cm and thereafter declined. Methane oxidation potential was maximum in the upper 10 cm and thereafter detected in reducing amounts. Molecular methods, based on the extraction of total DNA and its PCR amplification and hybridisation with specific phylogenetic 16S rRNA and functional gene specific primers and probes, were developed to analyse the methane producing and methane oxidising microbial communities. The functional gene sequences were based on methanogen methyl coenzyme reductase and methanotroph methane monooxygenase. Methanotrophs are located throughout the core whereas methanogens are restricted to the lower zones. The composition of the microbial communities is however complex consisting of a number of novel species not previously recognised and with the various species/sub-groups occupying different vertical zones.

KW - Methanogens

KW - Methanotrophs

KW - Microbial diversity

KW - Molecular probes

KW - Polymerase chain reaction

U2 - 10.1016/S1352-2310(98)00107-1

DO - 10.1016/S1352-2310(98)00107-1

M3 - Journal article

AN - SCOPUS:0032189517

VL - 32

SP - 3247

EP - 3255

JO - Atmospheric Environment

JF - Atmospheric Environment

SN - 1352-2310

IS - 19

ER -