11:00 〜 11:15
[ACG34-08] Lower anthropogenic fossil CH4 emissions inferred from multi-isotopic constraints on the global CH4 budget
★Invited Papers
キーワード:メタン、同位体、温室効果ガス、炭素循環、大気化学
Stable isotope measurements of atmospheric CH4 (δ13C-CH4, δD-CH4) have been utilized to resolve major three CH4 sources (i.e., biogenic, fossil fuel, and biomass burning sources) in the global CH4 budget. However, given the uncertainty of both the source isotope signatures and kinetic isotope effects, recent estimates of the global CH4 budget using stable isotope observations are still inconclusive. Radiocarbon measurements (Δ14C-CH4) could provide stronger additional constraint on the fossil-fuel CH4 sources (i.e., 14C-free), but the uncertainty of 14CH4 emissions from nuclear power facilities and a lack of data have limited such utilization. Here we present a new approach to estimate plausible global CH4 emissions and sinks scenarios over 1750–2015 using historical observations and Monte Carlo simulations of atmospheric CH4, δ13C-CH4, δD-CH4, and Δ14C-CH4. We utilize a particle filter (or Sequential Monte Carlo filter) approach to optimize the key 19 parameters of global CH4 sources and sinks. The ensemble members of CH4 source and sink scenarios, generated by the ensembles of 19 parameter combinations considering their uncertainties, were used to simulate atmospheric CH4, δ13C-CH4, δD-CH4, and Δ14C-CH4, and then retained when matching the historical observations. Our multi-isotopic model-data analysis suggests that current bottom-up estimates in natural and anthropogenic fossil and natural biogenic CH4 emissions are too high, whereas those in anthropogenic biogenic and biomass burning emissions are too low. The estimated global total fossil emission is also lower than the recent Δ14C-CH4-derived top-down estimates, but an independent estimate of global nuclear 14CH4 emissions would rather support our result. To obtain more robust estimates from multi-isotopic model-data analysis, many more global background observations of atmospheric δ13C-CH4, δD-CH4, and Δ14C-CH4, with their inter-laboratory measurement differences reduced, are indispensable to characterize their global representatives.