Simulation of preindustrial atmospheric methane to constrain the global source strength of natural wetlands

被引:69
作者
Houweling, S [1 ]
Dentener, F [1 ]
Lelieveld, J [1 ]
机构
[1] Univ Utrecht, Inst Marine & Atmospher Res Utrecht, NL-3584 CC Utrecht, Netherlands
关键词
D O I
10.1029/2000JD900193
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Previous attempts to quantify the global source strength of CH4 from natural wetlands have resulted in a range of 90-260 TE(CH4) yr(-1). This relatively uncertain estimate significantly limits our understanding of atmospheric methane. In this study we reduce this uncertainty by simulating preindustrial CH4 with a three-dimensional chemistry-transport model. Methane mixing ratios and delta(13)C-CH4, as deduced from ice cores, and estimates of other preindustrial sources and sinks, are used as constraints. This yields an average preindustrial natural wetland source strength of 163 Tg(CH4) yr(-1), with an estimated +/-2 sigma uncertainty range of 130-194 Tg(CH4) yr(-1). The present natural wetland source may be similar to 10% smaller, owing to drainage and cultivation of wetland area since 1800 A.D. The simulated pole-to-pole concentration difference is found to be rather insensitive to the assumed relative contributions of important preindustrial sources and sinks, and therefore imposes only a limited constraint on the estimate of natural wetland emissions. In contrast, delta(13)C-CH4 could provide robust constraints, but, unfortunately, at present reliable measurements are absent. Estimates of the historic development of anthropogenic CH4 sources, in combination with our model calculations, can largely explain the increase of methane mixing ratios during the nineteenth century. Results for the twentieth century indicate that these historical emission inventories underestimate anthropogenic emissions by at least 10%. Simulations of preindustrial and present-day isotopic ratios show that the growth of anthropogenic sources since 1800 A.D. may have increased delta(13)C-CH4 by 3 parts per thousand.
引用
收藏
页码:17243 / 17255
页数:13
相关论文
共 80 条
[1]   A time-averaged inventory of subaerial volcanic sulfur emissions [J].
Andres, RJ ;
Kasgnoc, AD .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D19) :25251-25261
[2]   TROPOSPHERIC OZONE IN THE 19TH-CENTURY - THE MONCALIERI SERIES [J].
ANFOSSI, D ;
SANDRONI, S ;
VIARENGO, S .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1991, 96 (D9) :17349-17352
[3]  
[Anonymous], GUID NAT GREENH GAS
[4]  
[Anonymous], 1993, GEOPHYS RES LETT
[5]  
[Anonymous], 1987, The Geophysiology of Amazonia: The Vegetation and Climate Interactions
[6]   GLOBAL DISTRIBUTION OF NATURAL FRESH-WATER WETLANDS AND RICE PADDIES, THEIR NET PRIMARY PRODUCTIVITY, SEASONALITY AND POSSIBLE METHANE EMISSIONS [J].
ASELMANN, I ;
CRUTZEN, PJ .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1989, 8 (04) :307-358
[7]   REVIEW AND ASSESSMENT OF METHANE EMISSIONS FROM WETLANDS [J].
BARTLETT, KB ;
HARRISS, RC .
CHEMOSPHERE, 1993, 26 (1-4) :261-320
[8]   A reevaluation of the open ocean source of methane to the atmosphere [J].
Bates, TS ;
Kelly, KC ;
Johnson, JE ;
Gammon, RH .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1996, 101 (D3) :6953-6961
[9]   Atmospheric gas concentrations over the past century measured in air from firn at the South Pole [J].
Battle, M ;
Bender, M ;
Sowers, T ;
Tans, PP ;
Butler, JH ;
Elkins, JW ;
Ellis, JT ;
Conway, T ;
Zhang, N ;
Lang, P ;
Clarke, AD .
NATURE, 1996, 383 (6597) :231-235
[10]   Global gridded inventories of anthropogenic emissions of sulfur and nitrogen [J].
Benkovitz, CM ;
Scholtz, MT ;
Pacyna, J ;
Tarrason, L ;
Dignon, J ;
Voldner, EC ;
Spiro, PA ;
Logan, JA ;
Graedel, TE .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1996, 101 (D22) :29239-29253