170 / 2025-04-13 17:32:14
Photochemical production of methane from cyanobacterial DOM in the presence of iron (oxyhydr)oxides
Methane paradox; Photo-methanification; Dissolved organic matter; Reactive oxygen species; Iron oxides
摘要待审
Xiaofei Zhu / State Key Laboratory of Geomicrobiology and Environmental Changes, School of Environmental Studies, China University of Geosciences, Wuhan 430078, China
Deng Liu / State Key Laboratory of Geomicrobiology and Environmental Changes, School of Environmental Studies, China University of Geosciences, Wuhan 430078, China
         The biological origin of methane (CH4) has traditionally been ascribed exclusively to the activity of methanogenic archaea in anaerobic environments. However, the emergence of the “CH4 paradox” has fundamentally challenged this paradigm, as a growing body of evidence documenting persistent CH4 emissions from oxygenated water columns of both marine and lacustrine systems. One plausible interpretations for this paradox is the photo-decomposition of dissolved organic matter (DOM) (i.e., photo-methanification) is a previously underestimated source for aquatic CH4 emissions. In aquatic systems, nano-sized iron (oxyhydr)oxidesare commonly found as suspended particles in aquatic systems, yet their potential influence on photo-methanification processes remains largely unknown.

          To address above knowledge gap, we conducted bench-scale experiments to investigate photo-methanification using DOM derived from a brackish cyanobacterium (Synechococcus elongatus) in the presence of idfferent iron (oxyhydr)oxides including hematite, magnetite, goethite, and ferrihydrite. Our results demonstrated that the hematite-supplemented DOM experimental system exhibited significant methanogenesis compared to the DOM-only control, with methane concentrations markedly higher than ambient background levels. And the DOM experimental systems supplemented with magnetite, goethite, and ferrihydrite exhibited marginal methanogenesis compared to the DOM-only control, with methane concentrations slightly higher than ambient background levels. These findings provide critical insights into the mechanisms driving aquatic CH4 emissions.

 
重要日期
  • 会议日期

    06月10日

    2025

    06月13日

    2025

  • 04月15日 2025

    初稿截稿日期

主办单位
National Natural Science Foundation of China
Geobiology Society
National Committee of Stratigraphy of China
Ministry of Science and Technology
Geological Society of China
Paleontological Society of China
Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences (CAS)
Institute of Vertebrate Paleontology and Paleoanthropology, CAS
International Commission on Stratigraphy
International Paleontological Association
承办单位
State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences (CUG, Wuhan)
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