Aerosols from Biomass Burning
Biomass burning is a globally important source of aerosols. Although burning
of vegetation occurs in temperate and boreal regions, emissions from these regions
are negligible in comparison to the tropics. The intensity of burning is greatest
in Africa, where savanna burning alone accounts for more than 40% of the total
biomass burned worldwide. Burning of forest during shifting agriculture and
during permanent land clearance produces emissions of a similar order of magnitude.
In addition, in the tropical regions the burning of fuel wood and agricultural
waste is the main energy source (as opposed to fossil fuels, etc.). A recent
analysis suggests that up to 3000 Tg of biofuel may be burned worldwide; it
is mainly used in developing regions experiencing rapid population growth. Recently
it was shown that vast amounts of a strongly light-absorbing carbonaceous aerosol
are emitted from the Indian subcontinent.
Biomass burning produces both primary aerosol particles and precursor gases
for secondary aerosol formation. About 70% of the mass of particulates released
is fine carbon-containing particles. In this particulate matter, most of the
carbon is in organic compounds, but up to about 20% occurs as black carbon
(elemental carbon, or "soot"). Globally, these emissions are important;
according to the IPCC, black carbon emitted worldwide from biomass burning is
similar in magnitude to that from fossil fuel burning (both ca. 6-9 Tg/yr).
Because they absorb light, black carbon aerosols are treated differently than
scattering aersols in studies of climate forcing .
Biomass burning may account for close to half 40% of the global emission of
anthropogenic VOC (volative organic carbon). The gaseous organic compounds released
during biomass burning condense easily (at low saturation values) and react
with each other to form aerosol particles. Gaseous hydrocarbons released during
combustion include ethane, propane, ethene and propene. Acetylene, methyl chloride.
and COS are also released from burning vegetation. Although COS is not a hydrocarbon,
it has a long atmospheric residence time, can be oxidixed to sulfate and contribute
to sulfate aerosol formation. The presence of polar functional groups, particularly
carboxylic and dicarboxylic acids, makes many of the organic compounds in aerosols
water-soluble and allows them to participate in cloud droplet nucleation.