Atmospheric Chemistry and Physics (Feb 2014)

Temporal changes in the emissions of CH<sub>4</sub> and CO from China estimated from CH<sub>4</sub> / CO<sub>2</sub> and CO / CO<sub>2</sub> correlations observed at Hateruma Island

  • Y. Tohjima,
  • M. Kubo,
  • C. Minejima,
  • H. Mukai,
  • H. Tanimoto,
  • A. Ganshin,
  • S. Maksyutov,
  • K. Katsumata,
  • T. Machida,
  • K. Kita

DOI
https://doi.org/10.5194/acp-14-1663-2014
Journal volume & issue
Vol. 14, no. 3
pp. 1663 – 1677

Abstract

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In situ observation of the atmospheric CO2, CH4, and CO mixing ratios at Hateruma Island (HAT, 24.05° N, 123.80° E) often show synoptic-scale variations with correlative elevations during winter, associated with air transport from the East Asian countries. We examine winter (November– March) trends in ΔCH4 / ΔCO2, ΔCO / ΔCO2, and ΔCO / ΔCH4 observed at Hateruma over the period 1999 to 2010. To investigate the relationship between the East Asian emissions and the short-term variations in the atmospheric mixing ratios, we use the FLEXPART Lagrangian particle dispersion model (LPDM). The observed ratios ΔCH4 / ΔCO2 and ΔCO / ΔCO2 both show an overall gradual decrease over the study period due to a recent rapid increase in fossil fuel consumption in China. We note, however, that the decreasing rates of ΔCH4 / ΔCO2 and ΔCO / ΔCO2 show gradual decrease and increase, respectively, during the entire observation periods used in this study. The ΔCO / ΔCH4 slope, on the other hand, shows an increasing trend during 1999–2004 but a decrease during 2005–2010. Calculation of the concentration footprint for the atmospheric observation at HAT by using the FLEXPART LPDM indicates that most of the short-term variations are caused by emission variations from northern and eastern China. Combined with a set of reported emission maps, we have estimated the temporal changes in the annual CH4 and CO emissions from China under the assumption that the estimate of the fossil-fuel-derived CO2 emissions based on the energy statistics are accurate. The estimated annual CH4 emissions, corresponding to nonseasonal sources or anthropogenic sources without rice fields, show a nearly constant value of 39 ± 7 TgCH4 yr−1 during 1998–2002, and then gradually increase to 46 ± 8 TgCH4 yr−1 in 2009/2010. The estimated annual CO emissions increase from 134 ± 32 TgCO yr−1 in 1998/1999 to 182 ± 42 TgCO yr−1 in 2004/2005, level off after 2005, and then slightly decrease to less than 160 TgCO yr−1 in 2008–2010.