Methane emissions may be driven by hydrogenotrophic methanogens inhabiting the stem tissues of poplar

Living trees in forests emit methane (CH4) from their stems. However, the magnitudes, patterns, drivers, origins, and biogeochemical pathways of these emissions remain poorly understood. We measured in situ CH4 fluxes in poplar stems and soils using static chambers and investigated the microbial communities of heartwood and sapwood by sequencing bacterial 16S, archaeal 16S, and fungal ITS rRNA genes. Methane emissions from poplar stems occurred throughout the sampling period. The mean CH4 emission rate was 2.7 mg m(-2) stem d(-1). Stem CH4 emission rate increased significantly with air temperature, humidity, soil water content, and soil CH4 fluxes, but decreased with increasing sampling height. The CO2 reduction and methylotrophic methanogenesis were the major methanogenic pathways in wood tissues. The dominant methanogen groups detected in stem tissues were Methanobacterium, Methanobrevibacter, Rice Cluster I, Methanosarcina, Methanomassiliicoccus, Methanoculleus, and Methanomethylophilaceae. In addition, three methanotrophic genera were identified in the heartwood and sapwood - Methylocystis, Methylobacterium, and Paracoccus. Overall, stem CH4 emissions can originate directly from the internal tissues or co-occur from soils and stems. The co-existence of methanogens and methanotrophs within heartwood and sapwood highlights a need for future research in the microbial mechanisms underlying stem CH4 exchange with the atmosphere.

Automated summary

Living trees in forests emit methane from their stems, with emissions influenced by temperature, humidity, soil moisture, and soil methane fluxes. Methane production in wood tissues primarily occurs through CO2 reduction and methylotrophic methanogenesis. Methanogen and methanotroph co-exist within heartwood and sapwood, highlighting the need for further research on the microbial mechanisms behind stem methane exchange with the atmosphere.