S. Houweling et al., Inverse modeling of methane sources and sinks using the adjoint of a global transport model, J GEO RES-A, 104(D21), 1999, pp. 26137-26160
An inverse modeling method is presented to evaluate the sources and sinks o
f atmospheric methane. An adjoint version of a global transport model has b
een used to estimate these fluxes at a relatively high spatial and temporal
resolution. Measurements from 34 monitoring stations and 11 locations alon
g two ship cruises by the National Oceanographic and Atmospheric Administra
tion have been used as input. Recent estimates of methane sources, includin
g a number of minor ones, have been used as a priori constraints. For the t
arget period 1993-1995 our inversion reduces the a priori assumed global me
thane emissions of 528 to 505 Tg(CH4) yr(-1) a posteriori. Further, the rel
ative contribution of the Northern Hemispheric sources decreases from 77% a
priori to 67% a posteriori. In addition to making the emission estimate mo
re consistent with the measurements, the inversion helps to reduce the unce
rtainties in the sources, Uncertainty reductions vary from 75% on the globa
l scale to similar to 1% on the grid-scale (8 degrees x10 degrees), indicat
ing that the grid scale variability is not resolved by the measurements. La
rge scale features such as the interhemispheric methane concentration gradi
ent are relatively well resolved and therefore impose strong constraints on
the estimated fluxes. The capability of the model to reproduce this gradie
nt is critically dependent on the accuracy at which the interhemispheric tr
acer exchange and the large-scale hydroxyl radical distribution are represe
nted. As a consequence, the inversion-derived emission estimates are sensit
ive to errors in the transport model and the calculated hydroxyl radical di
stribution. In fact, a considerable contribution of these model errors cann
ot be ignored. This underscores that source quantification by inverse model
ing is limited by the extent to which the rate of interhemispheric transpor
t and the hydroxyl radical distribution can be validated. We show that the
use of temporal and spatial correlations of emissions may significantly imp
rove our results; however, at present the experimental support for such cor
relations is lacking. Our results further indicate that uncertainty reducti
ons reported in previous inverse studies of methane have been overestimated
.