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    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1992
    In:  Journal of Geophysical Research: Atmospheres Vol. 97, No. D6 ( 1992-04-30), p. 6207-6217
    In: Journal of Geophysical Research: Atmospheres, American Geophysical Union (AGU), Vol. 97, No. D6 ( 1992-04-30), p. 6207-6217
    Abstract: We determined the distribution of gaseous and particulate sulfur compounds in the canopy of the tropical rain forest of northern Congo and the overlying atmosphere during February 12–25, 1988. Hydrogen sulfide and dimethylsulfide decayed exponentially with altitude from approximately 30–40 ppt at ground level to 3–5 ppt at around 3 km altitude. Emission fluxes from the forest to the atmosphere were estimated by fitting a one‐dimensional time‐dependent numerical model of chemistry and transport of the sulfur compounds to their observed vertical profiles. Emission fluxes of 0.6–1.0 nmol H 2 S m −2 min −1 and 0.3–0.7 nmol DMS m −2 min −1 were consistent with the observed vertical profiles of H 2 S and DMS. These fluxes compare well with fluxes reported previously for the Amazon rain forest during the dry season and support the view of a subordinate role of land biota in the global cycling of sulfur. The particulate sulfur concentration of 248 ppt was found below the forest canopy. Biomass burning is considered to be an important contributor to this particulate sulfur. Carbonyl sulfide was found to be enhanced above the 500 ppt tropospheric background throughout the mixing layer of 2–3 km depth, likely due to biomass burning.
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1992
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