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  • Anthropogenic sources  (1)
  • long-range transport  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pure and applied geophysics 116 (1978), S. 244-273 
    ISSN: 1420-9136
    Keywords: Anthropogenic sources ; Budget ; Natural sources ; Organic matter
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract Perhaps less is known about the global source, distribution, and fluxes of non-methane organic matter than any other major class of chemical substances in the atmosphere. Source strength estimates and consideration of the available concentration data suggest that the quantity of organic carbon on large particles (d〉1 μm) in the global troposphere can be explained by primary emissions from anthropogenic sources and such natural sources as the ocean, crustal weathering, and forest wildfires. However, these pollution and natural sources apparently cannot account for the global tropospheric burden of small particle (d〈1 μm) organic carbon. Approximately 80–160 MT/yr of small particle carbon from some additional source is required to balance this cycle. Possibilities include direct production from the leaves of vegetation and gas to particle conversion of natural and anthropogenic organic carbon compounds. The estimated production of reactive vapor phase organic compounds from natural and pollution sources is sufficient to account for the mass of this additional small particle organic carbon. However, considerably more data is required on the global distribution, source strengths, reaction pathways and rates, and removal mechanisms before an accurate description of the non-methane organic carbon cycle can be made.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of atmospheric chemistry 3 (1985), S. 123-138 
    ISSN: 1573-0662
    Keywords: Annual dust flux ; mineral aerosol ; North Pacific ; spatial distribution ; long-range transport ; Asian dust ; marine sediments
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Total deposition of atmospheric mineral particles (wet plus dry) has been measured during consecutive two-week sampling intervals from January, 1981 to March, 1982 at four island stations (Midway, Oahu, Enewetak, and Fanning) of the SEAREX Asian Dust Study Network in the North Pacific. The total deposition of mineral aerosol during the period from February to June is higher than that during the period from July to January at most of the stations. A systematic geographical trend is apparent in the dust flux, with greater fluxes at higher latitudes. The deposition values are correlated with the atmospheric mineral particle concentrations at these stations. The mineral particles are transported from arid regions in Asia to the North Pacific, and the annual dust deposition to the ocean appears to be dominated by sporadic dust events of short duration. Wet deposition dominates the removal of dust particles from the atmosphere over the North Pacific. The total deposition of atmospheric mineral material to the central North Pacific is estimated to be ∼20×1012 g yr-1.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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