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Titel Natural abundance and 13C-enriched characterisation of atmospheric methane uptake in a forest soil
VerfasserIn Peter Maxfield, Edward Hornibrook, Richard Evershed
Konferenz EGU General Assembly 2013
Medientyp Artikel
Sprache Englisch
Digitales Dokument PDF
Erschienen In: GRA - Volume 15 (2013)
Datensatznummer 250084017
 
Zusammenfassung
Whilst much attention is focused on CH4 emission inventories, CH4 sinks are sometimes overlooked and not accurately accounted for in national budgets. Two primary reasons for this disjunction include uncertainties about the magnitude and mechanism of terrestrial CH4 oxidation, and an under-appreciation of the quantity of CH4 that is removed from the atmosphere by microorganisms. These uncertainties in part are caused by a lack of high-resolution field data that quantify microbial soil CH4 sink. To fully characterize the soil CH4 sink, isotopic fractionation of CH4during uptake and the fate of CH4 carbon following oxidation by soil microorganisms should be quantified in addition to CH4 fluxes. Here we report on field tests studying CH4 uptake in soil using a Picarro G2201-i cavity ringdown spectrometer (CRDS). Short term atmospheric CH4 uptake was continuously measured in a forest soil in Leigh Woods, UK where the soil methanotrophic community and soil CH4 uptake kinetic isotopic effect (KIE) had been previously quantified using stable isotope probing and conventional stable isotope analysis techniques (Maxfield et al., 2008). Two methodological approaches were tested: (i) direct measurement of the soil CH4 uptake KIE at subambient CH4 concentrations, and (ii) methanotrophic carbon conversion efficiency (CCE) where CCE was evaluated through monitoring the direct conversion of 13C-labelled CH4 to 13C-labelled CO2. The suitability of the G2201-i analyzer as a continuous isotopic CH4 and CO2 analyzer for use at both subambient CH4 concentrations and high 13C-enrichments will be discussed. Maxfield, P.J., Evershed, R.P. and Hornibrook, E.R.C. (2008) Physical and biological controls on the in situ kinetic isotope effect associated with oxidation of atmospheric CH4 in mineral soils. Environmental Science & Technology, 42, 7824-7830.