Aerosol emissions from forest and grassland burnings in the southern amazon basin and central Brazil

Abstract

Forest and grassland clearing by means of prescribed fires in tropical areas of the world may be responsible for large inputs of fine particulates to the global atmosphere besides being a major source of trace gases. The major continents on which extensive biomass burning takes place are Africa and South America. Such agricultural practices of burning have been employed throughout man's existence, but the importance and significance of such burning relative to anthropogenic industrial emissions to the atmosphere has not until extremely recently been seriously studied. In August–September 1979 project “Brushfire 1979” took place based in Brasília, Brazil. The Air Quality Division of the National Center for Atmospheric Research made ground level and aircraft measurements of trace gases (e.g. CO 2, CO, CH 4, N 2O, H 2, CH 3Cl, COS, NO, NO 2, O 3) and Florida State University sampled ground level aerosol emissions from grass and forest burnings. Aerosols were sampled using plastic 7-stage single orifice cascade impactors and FSU type linear and circular “streakers”. Long term sampling was made of regional background for total particulates (<15 μmad) with 2 h resolution using streakers and with impactors for 24 h resolution of 7 particle size fractions (<0.25 to >8 μmad). Short term sampling within grass or forest fires was made using impactors incorporated into portable kits containing 4 miniature 12–18 V dc Brailsford pumps and a disposable dry cell power pack. Sampling times of 5–15 min were found optimal under these conditions. Grass fires were sampled in the savannah area northeast of Brasília and forest fires in the state of Mato Grosso on the southern edge of the dryland forest of the Amazon basin. Residual ash samples were collected. All of the samples were analyzed at Florida State University using PIXE for 15–20 elements including Mg, Al, Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Br, Pb and Sr. Computer reduction of the X-ray spectra was made using the “HEXB” program. One of the prominent features found was the large flux of small particles (<2.0 μm) from both fire types. P, S and Cl were mostly small particle, Mg, Al, Si and K showed a bimodal distribution biased towards the small particle range, while Ca, Ti and Fe (crustal elements) predominated in the large particle mode. As Cl was found to be exclusively small particle, a formation mechanism in which HCl gas neutralizes small organic particles containing P and S may be hypothesized. A much more extensive field program for the summer of 1980 is planned to take place in the central Amazon basin using ground and airborne aerosol samplers, to capitalize on the work pioneered in this study.