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  • 2020-2024  (1)
  • 1965-1969  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 3 (1969), S. 1207-1210 
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naturwissenschaften 54 (1967), S. 110-113 
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Notes: Summary Atmospheric samples have been analyzed for iodine, bromine, and chlorine by neutron activation analysis. Aerosols of marine origin, derived from sea spray, are found to contain the halogens in relative proportions different from sea water, and data from Hawaii and winter northern Alaska indicate fractionation of the elements both during transfer across the sea-air interface and by chemical reactions in the atmosphere. The ratio Br/Cl is usually severalfold greater in aerosols over land than in sea water (Br/Cl=0.0034), but over open sea water it is less. In general, the ratio I/Br exhibits a greater degree of constancy (values cluster in the region I/Br ∼ 0.1–0.2) than does either I/Cl or Br/Cl, suggesting a long residence time and a coherence of I and Br in their movement as particulate material in the atmosphere. However, a singularly effective sea-air transfer mechanism for iodine is indicated by its generally high atmospheric concentration compared to sea water (I/Br=0.001). Bromine of pollution origin and associated with lead has been observed in aerosols from Cambridge, Massachusetts. Chlorine and iodine concentrations are similar to the Hawaii values and provide a basis for resolving excess pollution bromine from the natural marine component. The ratio (excess Br)/Pb in aerosols appears to be correlated directly with the haziness of the air.
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 2024-02-07
    Description: The discovery of atmospheric micro(nano)plastic transport and ocean–atmosphere exchange points to a highly complex marine plastic cycle, with negative implications for human and ecosystem health. Yet, observations are currently limited. In this Perspective, we quantify the processes and fluxes of the marine-atmospheric micro(nano)plastic cycle, with the aim of highlighting the remaining unknowns in atmospheric micro(nano)plastic transport. Between 0.013 and 25 million metric tons per year of micro(nano)plastics are potentially being transported within the marine atmosphere and deposited in the oceans. However, the high uncertainty in these marine-atmospheric fluxes is related to data limitations and a lack of study intercomparability. To address the uncertainties and remaining knowledge gaps in the marine-atmospheric micro(nano)plastic cycle, we propose a future global marine-atmospheric micro(nano)plastic observation strategy, incorporating novel sampling methods and the creation of a comparable, harmonized and global data set. Together with long-term observations and intensive investigations, this strategy will help to define the trends in marine-atmospheric pollution and any responses to future policy and management actions.
    Type: Article , PeerReviewed
    Format: other
    Format: text
    Format: text
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