Ozone production due to emissions from vegetation burning

Ozone has been observed in elevated concentrations by satellites over areas previously believed to be background. There is meteorological evidence, that these ozone plumes found over the Atlantic Ocean originate from vegetation fires on the African continent.In a previous study (DECAFE-88), we have investigated ozone and assumed precursor compounds over African tropical forest regions. Our measurements revealed large photosmog layers at altitudes from 1.5 to 4 km. Both chemical and meteorological evidence point to savanna fires up to several thousand km upwind as sources.Here we describe ozone mixing ratios observed over western Africa and compare ozone production ratios from different field measurement campaigns related to vegetation burning. We find that air masses containing photosmog ingredients require several days to develop their oxidation potential, similar to what is known from air polluted by emissions from fossil fuel burning. Finally, we estimate the global ozone production due to vegetation fires and conclude that this source is comparable in strength to the stratospheric input.     

Production of N2O,CH4, and CO2 from soils in the tropical savanna during the dry season

Emissions of N₂O, CH₄, and CO₂ from soils at two sites in the tropical savanna of central Venezuela were determined during the dry season in February 1987. Measured arithmetic mean fluxes of N₂O, CH₄, and CO₂ from undisturbed soil plots to the atmosphere were 2.5×10⁹, 4.3×10¹⁰, and 3.0×10¹³ molecules cm^-2 s^-1, respectively. These fluxes were not significantly affected by burning the grass layer. Emissions of N₂O increased fourfold after simulated rainfall, suggesting that production of N₂O in savanna soils during the rainy season may be an important source for atmospheric N₂O. The CH₄ flux measurements indicate that these savanna soils were not a sink, but a small source, for atmospheric methane. Fluxes of CO₂ from savanna soils increased ninefold two hours after simulated rainfall, and remained three times higher than normal after 16 hours. More research is needed to clarify the significance of savannas in the global cycles of N₂O, CH₄, CO₂, and other trace gases, especially during the rainy season.     

Field studies of methane emission from termite nests into the atmosphere and measurements of methane uptake by tropical soils

The flux of CH₄ and CO₂ from termite nests into the atmosphere has been measured in a broad-leafed-type savannah in South Africa. Measurements were carried out on nests of species of six genera, i.e., Hodotermes, Macrotermes, Odontotermes, Trinervitermes, Cubitermes, and Amitermes. The flux rates of CH₄ relative to the flux rate of CO₂ in terms of carbon obtained for the individual species showed ratios of 2.9×10^-3, 7.0×10^-4, 6.7×10^-5, 8.7×10^-3, 2.0×10^-3 and 4.2×10^-3, respectively. Using data published on the assimulation efficiencies of termites, the flux of carbon as CH₄ accounts for 6.0×10^-5 to 2.6×10^-3 of the carbon ingested which results in a global CH₄ emission by termites of 2 to 5×10¹² g/yr. Methane is decomposed in the soil with average decomposition rates of 52 g/m²/h. The annual CH₄ consumption in the tropics and subtropics is estimated to be 21×10¹² g which exceeds the CH₄ emission rate by termites.     

Trace Gas Measurements Between Moscow and Vladivostok Using the Trans-Siberian Railroad

Using a laboratory wagon traveling along the Trans-Siberian railroad, O₃, NO, NO₂, CO, CH₄, SF₆ and black carbon aerosol have been measured during the summer of 1996. The expedition from Niznij Novgorod (500 km east of Moscow) to Vladivostok (and back to Moscow) has shown the great potential of the train method; here the first results are presented and discussed. A wealth of boundary layer air data was obtained during the over 18000 km travel without serious contamination problems from the electric train itself. The diurnal O₃ cycle peaked generally below 50 nmole/mole, showed the effects of changes in J(NO₂), and often dropped to a few nmole/mole at night time during inversions. Over the vast Siberian lowlands situated between the Ural mountains and the river Yenisey, CH₄ levels were consistently elevated at around 1.95 µmole/mole, which we mainly attribute to wetland emissions. Over eastern Siberia, however, CH₄ levels were generally lower at 1.85 µmole/mole. In contrast, over the west Siberian lowlands, CO levels were relatively low, often reaching values of only 110 nmole/mole, whereas over eastern Siberia CO levels were higher. Very high CO levels were detected over a 2000 km section east of Chita, along the river Amur, which represented an enormous polluted air mass. ¹⁴C analysis performed on several CO samples confirms that the origin was biomass burning. SF₆, which was measured as a general conserved tracer, showed an eastward attenuation from 4.0 to 3.9 pmole/mole, with peaks in a number of places due to local Russian emissions.     

N2O measurements of air extracted from antarctic ice cores: Implication on atmospheric N2O back to the last glacial-interglacial transition

A method has been developed for determining the N₂O concentrations of air bubbles trapped in ice cores. The air is removed by cutting ice samples of about 45 cm³ with a rotating knife, under pure nitrogen. About 2 cm³ of the gas extracted from the ice is analyzed. The N₂O concentrations are measured by gas chromatography, using electron capture detection with a detection limit of approximately 1 ppbv. The accuracy of the analysis is lower than 6%.This method has been used to analyze 34 Antarctic ice samples. Twelve air samples are from the D57 core and date approximately from AD 1600 and 1900. Data indicate a concentration of about 270 ppbv approximately 400 years ago, and of about 293 ppbv for the beginning of the 20th Century. The other samples have been taken from the Dome C core and date back to the time period extending from the Holocene to the Last Glacial Maximum. The results obtained for the Holocene period are in very good agreement with the concentrations measured for the pre-industrial time from the D57 core and indicate that, during the Holocene period, atmospheric N₂O mixing ratios may have remained fairly constant. The value observed during the last climatic transition suggest a slight increase in the N₂O concentrations when the climate was warming up. The results obtained on samples formed during the Last Glacial Maximum show high scattering which is best explained by the bad quality of this part of the core.     

Methane emission from rice paddies

Methane release rates from rice paddies have been measured in Andalusia, Spain, during almost a complete vegetation period in 1982 using the static box system. The release rates ranged between 2 and 14 mg/m²/h and exhibited a strong seasonal variation with low values during the tillering stage and shortly before harvest, while maximum values were observed at the end of the flowering stage. The CH₄ release rate, averaged over the complete vegetation period, accounted for 4 mg/m²/h which results in a worldwide CH₄ emission from rice paddies of 35–59×10¹² g/yr if we assume that the observed CH₄ release rates are representative of global conditions. The CH₄ release rates showed diurnal variations with higher values late in the afternoon which were most likely caused by temperature variations within the upper layers of the paddy soils. Approximately 95% of the CH₄ emitted into the atmosphere by rice paddies was due to transport through the rice plants. Transport by bubbles or diffusion through the paddy water was of minor importance. Incubation experiments showed that CH₄ was neither produced nor consumed in the paddy water. The relase of CH₄ from rice paddies caused a diurnal variation of CH₄ in ambient air within the rice-growing area with maximum values of up to 2.3 ppmv during the early morning, compared to average daytime values of 1.75 ppmv.     

Airborne measurements of savanna fire emissions and the regional distributio of pyrogenic pollutants over Western Africa

We measured CO₂, CO, CH₄, H₂, and NO₂ in air masses polluted by savanna fires over Côte d'Ivoire, western Africa. Elevated concentrations of these trace gases were found in fire plumes and also in extensive haze layers. Trace gas mixing ratios ranged as high as 605 ppmv for CO₂, 14.8 ppmv for CO, 2.7 ppmv for CH₄, 4.2 ppmv for H₂, and 25 ppbv for NO₂. We compare our emission ratios to those obtained in previous field and laboratory studies. The emission ratios, expressed as an average and as a range or as an average only, were: dCO/dCO₂ 5.3×10^–2 (3–18×10^–2); dCH₄/dCO 5.3×10^–2; dH₂/dCO 2.4×10^–1 and dNO₂/dCO₂ 1.8×10^–4 (1.5–2.2×10^–4). The values found match those found during similar measurements, though our results point to rather vigorous burning in the savanna of western Africa.