Pulsed biogenic methane emissions coupled with episodic warming during the Toarcian Oceanic Anoxic Event

R Ruoyuan Qiu (Key Laboratory of Deep Petroleum Intelligent Exploration and Development, Institute of Geology and Geophysics, Chinese Academy of Sciences) Z Zhichao Yu (Key Laboratory of Deep Petroleum Intelligent Exploration and Development, Institute of Geology and Geophysics, Chinese Academy of Sciences) B Benjamin J. W. Mills (School of Earth and Environment, University of Leeds) R Renda Huang (Institute of Energy, Peking University) W Wang Zhang (College of Materials Science and Engineering, College of Environment, State Key Laboratory of Advanced Separation Membrane Materials, Zhejiang Key Laboratory of Low-carbon Control Technology for Industrial Pollution) T Terry Isson (Environmental Research Institute, University of Waikato) B Bo Wan (State Key Laboratory of Lithospheric and Environmental Coevolution, Institute of Geology and Geophysics, Chinese Academy of Sciences) R Ruizhen Zhang (Key Laboratory of Deep Petroleum Intelligent Exploration and Development, Institute of Geology and Geophysics, Chinese Academy of Sciences) M Mingyu Zhao (Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology, Department of Chemical Engineering) Z Zhijun Jin

Abstract

Reconstructing carbon release fluxes during ancient climatic warming events is important for improving predictions of carbon cycle and climate dynamics under future anthropogenic warming scenarios. We investigate the extent of biogenic methane release and its contribution to climate variability across the Toarcian Oceanic Anoxic Event (T-OAE) approximately 183 million years ago. To do this, we developed a global biogeochemical model and applied a Bayesian inversion using Markov Chain Monte Carlo (MCMC) simulations. Based on a high-resolution record of carbon isotope excursions from the Yorkshire section, our results indicate that a release of at least 4,700 Gt carbon from biogenic CH 4 (with a carbon isotopic composition, δ 13 C of −50 to −70‰) is necessary to accurately reproduce the pronounced pulsed shift in the δ 13 C, as well as the inferred changes in atmospheric p CO 2 and global temperature. This massive methane release may have led to a substantial increase in atmospheric p CH 4 and contributed to additional global surface warming, perhaps by more than 2 °C. We further elucidate that the liberation of methane may have been facilitated by an upsurge in methanogenesis alongside a concomitant decline in methane oxidation within organic-rich, sulfate-depleted marine environments. An active CH 4 cycle represents a positive feedback mechanism that exacerbates environmental deterioration during climatic warming events, ultimately contributing to mass extinction of marine life.

Article Details

Volume / Issue Vol. 122, Issue 36
Published September 09, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (10)

R

Ruoyuan Qiu

Key Laboratory of Deep Petroleum Intelligent Exploration and Development, Institute of Geology and Geophysics, Chinese Academy of Sciences

Z

Zhichao Yu

Key Laboratory of Deep Petroleum Intelligent Exploration and Development, Institute of Geology and Geophysics, Chinese Academy of Sciences

B

Benjamin J. W. Mills

School of Earth and Environment, University of Leeds

R

Renda Huang

Institute of Energy, Peking University

W

Wang Zhang

College of Materials Science and Engineering, College of Environment, State Key Laboratory of Advanced Separation Membrane Materials, Zhejiang Key Laboratory of Low-carbon Control Technology for Industrial Pollution

T

Terry Isson

Environmental Research Institute, University of Waikato

B

Bo Wan

State Key Laboratory of Lithospheric and Environmental Coevolution, Institute of Geology and Geophysics, Chinese Academy of Sciences

R

Ruizhen Zhang

Key Laboratory of Deep Petroleum Intelligent Exploration and Development, Institute of Geology and Geophysics, Chinese Academy of Sciences

M

Mingyu Zhao

Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology, Department of Chemical Engineering

Z

Zhijun Jin