ABSTRACT
On the Qinghai–Tibetan Plateau, isotopic signatures in soil–atmosphere CH4 fluxes were investigated in nine grasslands and three wetlands. In the grasslands, the fractionation factor for soil CH4 uptake, αsoil, was much smaller than the usually reported value of 0.9975–1.0095. Stepwise multiple variation analysis indicates that αsoil is higher for higher soil water contents but is lower for higher C/N ratios of soil surface biomass. In the three wetlands, the soil-emitted δ13C–CH4 was similar (−55.3 ± 5.5 ‰ and −53.0 ± 5.5 ‰) in two bogs separated by >1000 km but was lower (−63.4 ± 6.3 ‰) in a marsh. Environmental factors related to intrasite variations in soil-emitted δ13C–CH4 include the soil C/N ratio, oxidation–reduction potential, soil C concentration and soil water contents. Geographical isotopic surveys revealed environmental constraints on the CH4 consumption pathways in grasslands and the biome type-specific consistency in CH4 production pathways in wetlands.
Acknowledgements
The authors thank Assoc. Prof. S. Toyoda in the Department of Environmental Science and Technology, Tokyo Institute of Technology and Ms. N. Suzuki and other members in Prof. N. Yoshida’s laboratory in the Department of Environmental Chemistry and Engineering, Tokyo Institute of Technology, for providing help and instruments for isotope measurements of the CH4 gas. The authors also thank Assoc. Prof. M. Hirota, University of Tsukuba and Prof. S. Mariko, Hosei University, for providing the instruments and advice to measure CH4 gas concentrations.
Disclosure statement
No potential conflict of interest was reported by the authors.
ORCID
Tomomichi Kato http://orcid.org/0000-0003-3757-3243