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Three‐dimensional model synthesis of the global methane cycle
Author(s) -
Fung I.,
John J.,
Lerner J.,
Matthews E.,
Prather M.,
Steele L. P.,
Fraser P. J.
Publication year - 1991
Publication title -
journal of geophysical research: atmospheres
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.67
H-Index - 298
eISSN - 2156-2202
pISSN - 0148-0227
DOI - 10.1029/91jd01247
Subject(s) - methane , atmospheric methane , environmental science , atmospheric sciences , atmosphere (unit) , tundra , flux (metallurgy) , greenhouse gas , carbon cycle , ecosystem , geology , meteorology , chemistry , physics , arctic , ecology , oceanography , organic chemistry , biology
The geographic and seasonal emission distributions of the major sources and sinks of atmospheric methane were compiled using methane flux measurements and energy and agricultural statistics in conjunction with global digital data bases of land surface characteristics and anthropogenic activities. Chemical destruction of methane in the atmosphere was calculated using three‐dimensional OH fields every 5 days taken from Spivakovsky et al. (1990a, b) . The signatures of each of the sources and sinks in the atmosphere were simulated using a global three‐dimensional tracer transport model. Candidate methane budget scenarios were constructed according to mass balance of methane and its carbon isotopes. The verisimilitude of the scenarios was tested by their ability to reproduce the meridional gradient and seasonal variations of methane observed in the atmosphere. Constraints imposed by all the atmospheric observations are satisfied simultaneously by several budget scenarios. A preferred budget comprises annual destruction rates of 450 Tg by OH oxidation and 10 Tg by soil absorption and annual emissions of 80 Tg from fossil sources, 80 Tg from domestic animals, and 35 Tg from wetlands and tundra poleward of 50°N. Emissions from landfills, tropical swamps, rice fields, biomass burning, and termites total 295 Tg; however, the individual contributions of these terms cannot be determined uniquely because of the lack of measurements of direct fluxes and of atmospheric methane variations in regions where these sources are concentrated.

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