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  • Annual dust flux  (1)
  • marine aerosols  (1)
  • 1
    ISSN: 1573-0662
    Keywords: Nitrate ; marine aerosols ; South Pacific ; sources ; 210Pb ; 1Be ; non-sea-salt sulfate ; trajectories
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Weekly bulk aerosol samples collected at Funafuti, Tuvalu (8°30′S, 179°12′E), American Samoa (14°15′S, 170°35′W), and Rarotonga (21°15′S, 159°45′W), from 1983 through most of 1987 have been analyzed for nitrate and other constituents. The mean nitrate concentration is about 0.11 μg m−3 at each of these stations: 0.107±0.011 μg m−3 at Funafuti; 0.116±0.008 at American Samoa; and 0.117±0.010 at Rarotonga. Previous measurements of mineral aerosol and trace metal concentrations at American Samoa are among the lowest ever recorded for the near-surface troposphere and indicate that this region is minimally affected by transport of soil material and pollutants from the continents. Consequently, the nitrate concentration of 0.11 μg m−3 can be regarded as the natural level for the remote marine boundary layer of the tropical South Pacific Ocean. In contrast, over the tropical North Pacific which is significantly impacted by the transport of material from Asia and North America, the mean nitrate concentrations are about three times higher, 0.29 and 0.36 μg m−3 at Midway and Oahu, respectively. The major sources of the nitrate over the tropical South Pacific are still very uncertain. A very significant correlation between the nitrate concentrations at American Samoa and the concentrations of 210Pb suggests that transport from continental sources might be important. This continental source could be lightning, which occurs most frequently over the tropical continents. A near-zero correlation with 7Be indicates that the stratosphere and upper troposphere are probably not the major sources. A significant biogenic source would be consistent with the higher mean nitrate concentrations, 0.16 to 0.17 μg m−3, found over the equatorial Pacific at Fanning Island (3°55′N, 159°20′W) and Nauru (0°32′S, 166°57′E). The lack of correlation between nitrate and nss sulfate at American Samoa does not necessarily preclude an important role for marine biogenic sources.
    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
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