Methane Distribution, Production, and Emission in the Western North Pacific

Author:

Wang Hao‐Nan12ORCID,Du Guan‐Xiang2,Yu Shu‐Xian23ORCID,Zhang Hong‐Hai12ORCID,Song Guo‐Dong12ORCID,Liu Su‐Mei12,Zheng Nan4,Zhang Xiao‐Hua23ORCID,Zhang Gui‐Ling12ORCID

Affiliation:

1. Frontiers Science Center for Deep Ocean Multispheres and Earth System Key Laboratory of Marine Chemistry Theory and Technology Ministry of Education Ocean University of China Qingdao China

2. Laboratory for Marine Ecology and Environmental Science Qingdao Marine Science and Technology Center Qingdao China

3. College of Marine Life Sciences Ocean University of China Qingdao China

4. National Marine Environmental Monitoring Center Dalian China

Abstract

AbstractThe ocean is a source of atmospheric methane (CH4), but there are still large uncertainties in the estimations of global oceanic CH4 emission due to sparse data coverage. In this study, we investigated the spatial distribution and influencing factors of CH4 in the Western North Pacific (WNP) during May–June 2021. High‐resolution continuous underway measurements showed that surface CH4 concentrations indicated an obvious spatial gradient with an increase from the south to the north due to the influence of water mixing between Kuroshio Extension (KE) and Oyashio. Surface water was generally oversaturated with respect to the atmospheric CH4, and high CH4 fluxes occurred in the Kuroshio‐Oyashio transition region due to high productivity and intensive air‐sea interaction, emphasizing the importance of the Kuroshio‐Oyashio transition region in global oceanic CH4 emission. Vertically, subsurface CH4 maximums were observed around 50–300 m due to in situ production through multiple pathways, and their distributions in the water column were affected by subduction of North Pacific Intermediate Water (NPIW) and advective transport. Methylphosphonate (MPn) enrichment experiment and 16S rRNA gene sequencing showed that in subtropical region and Kuroshio‐Oyashio transition region, Vibrio spp. might produce CH4 by degrading MPn. Although this process was inhibited by inorganic phosphorus and regulated by iron stress, it might be a potential source of CH4 in the oxygenated water in the WNP. Our results contribute to better constrain the global oceanic CH4 emission, and help understanding the role of biological and physical processes in regulating CH4 emission in the WNP.

Publisher

American Geophysical Union (AGU)

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