Nitrous Oxide Formation and Consumption in Thawing Permafrost: A Microcosm Study
Yanchen SuniD, Xiaofen WuiD, Oksana G. ZaninaiD, Elizaveta RivkinaiD, Karen G. LloydiD, Frank E. LöffleriD, Tatiana A. VishnivetskayaiD
Abstract
Nitrous oxide (N2O) emissions contribute to stratospheric ozone depletion and global warming. Climate warming causes permafrost thawing and decomposition of the dormant nitrogenous compounds, releasing N2O; however, understanding of the microbial formation and consumption of N2O in permafrost is still limited. Permafrost soils collected at two depths (5.4 m and 16.9 m) from the East Siberian Sea coast of Russia were used to establish microcosms assessing N2O formation and consumption in the presence of either nitrate (NO3-, 1 mM) or N2O (1 mM), respectively, during incubation at 4 and 20{degrees}C. Rapid N2O formation was observed in NO3--amended microcosms, but N2O consumption was slow and incomplete over a 1-year incubation period in all microcosms. Twenty-six quality-filtered metagenome-assembled genomes (MAGs) harboring genes involved in the reduction of NO3- and/or N2O were recovered from 16 metagenomes obtained from duplicate NO3-- and N2O-amended microcosms. None of the MAGs carried a complete set of genes to perform canonical denitrification (i.e., NO3-[->]N2) indicating N2O formation and consumption is likely driven by non-denitrifying bacteria. While coastal permafrost microbiomes harbor nosZ genes, activity monitored in the microcosms indicates N2O formation exceeds N2O consumption, emphasizing the need for integrated approaches to assess and predict N turnover in thawing permafrost.
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