The contribution of terrestrial sources and sinks to trends in the seasonal cycle of atmospheric carbon dioxide

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Increased plant growth in the northern high latitudes from 1981 to 1991

R. Myneni, C. D. Keeling, C J Tucker … (1997)

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Biomass burning in the tropics: impact on atmospheric chemistry and biogeochemical cycles.

P. CRUTZEN, M. Andreae (1990)

Biomass burning is widespread, especially in the tropics. It serves to clear land for shifting cultivation, to convert forests to agricultural and pastoral lands, and to remove dry vegetation in order to promote agricultural productivity and the growth of higher yield grasses. Furthermore, much agricultural waste and fuel wood is being combusted, particularly in developing countries. Biomass containing 2 to 5 petagrams of carbon is burned annually (1 petagram = 10(15) grams), producing large amounts of trace gases and aerosol particles that play important roles in atmospheric chemistry and climate. Emissions of carbon monoxide and methane by biomass burning affect the oxidation efficiency of the atmosphere by reacting with hydroxyl radicals, and emissions of nitric oxide and hydrocarbons lead to high ozone concentrations in the tropics during the dry season. Large quantities of smoke particles are produced as well, and these can serve as cloud condensation nuclei. These particles may thus substantially influence cloud microphysical and optical properties, an effect that could have repercussions for the radiation budget and the hydrological cycle in the tropics. Widespread burning may also disturb biogeochemical cycles, especially that of nitrogen. About 50 percent of the nitrogen in the biomass fuel can be released as molecular nitrogen. This pyrdenitrification process causes a sizable loss of fixed nitrogen in tropical ecosystems, in the range of 10 to 20 teragrams per year (1 teragram = 10(12) grams).

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Observational contrains on the global atmospheric co2 budget.

P Tans, I. Fung, T Takahashi (1990)

Observed atmospheric concentrations of CO(2) and data on the partial pressures of CO(2) in surface ocean waters are combined to identify globally significant sources and sinks of CO(2). The atmospheric data are compared with boundary layer concentrations calculated with the transport fields generated by a general circulation model (GCM) for specified source-sink distributions. In the model the observed north-south atmospheric concentration gradient can be maintained only if sinks for CO(2) are greater in the Northern than in the Southern Hemisphere. The observed differences between the partial pressure of CO(2) in the surface waters of the Northern Hemisphere and the atmosphere are too small for the oceans to be the major sink of fossil fuel CO(2). Therefore, a large amount of the CO(2) is apparently absorbed on the continents by terrestrial ecosystems.