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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 31 (1959), S. 884-886 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 250 (1974), S. 563-565 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Two other ways have been suggested in which reversals of the Earth's magnetic field could influence evolution. One way is by the direct biological effect of a magnetic field on organisms; there is a short discussion of this by Grain11. The second mechanism proposes that a reversal of the Earth's ...
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 380 (1996), S. 416-419 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Climate models incorporating aerosols suggest that anthropogenic non-seasalt sulphate (n.s.s. SO2") aerosols in the Northern Hemisphere scatter as much as 1-2 Wm2 of incoming solar radiation back to space24, yielding a cooling rate comparable to the heating rates attributed to greenhouse ...
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Earth and Planetary Science Letters 87 (1988), S. 367-378 
    ISSN: 0012-821X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 350 (1991), S. 221-223 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The sulphate ion is the oxidative endmember of the atmos-pheric sulphur cycle and it is one of the principal species in aerosols and precipitation over large areas of the Earth. Globally, anthropogenic emissions of SO2 are the largest source of atmospheric sulphur4 whereas the second largest source ...
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  • 6
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 317 (1985), S. 516-518 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Chester et al.8 were able to distinguish between and characterize dust source types in the Mediterranean region by plotting aluminium concentration against the magnetic susceptibility/aluminium concentration quotient. Soil-derived dusts of North African origin fell at one extreme, with high ...
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  • 7
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 289 (1981), S. 570-572 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] A seasonal meteorological control on African dust transport can be inferred from a 15-yr mineral aerosol study10 carried out on Barbados, West Indies (1310'N, 5930'W). There is a pronounced annual cycle in dust concentration with the maximum occurring during the summer; monthly mean winter ...
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  • 8
    ISSN: 1573-0662
    Keywords: Antarctica ; Palmer ; Marsh ; Mawson ; aerosol particles ; biogeochemical cycles ; sulfate ; nitrate ; methanesulfonate ; lead-210 ; beryllium-7 ; sea-salt ; ammonium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract High volume bulk aerosol samples were collected continuously at three Antarctic sites: Mawson (67.60° S, 62.50° E) from 20 February 1987 to 6 January 1992; Palmer Station (64.77° S, 64.06° W) from 3 April 1990 to 15 June 1991; and Marsh (62.18° S, 58.30° W) from 28 March 1990, to 1 May 1991. All samples were analyzed for Na+, SO 4 2− , NO 3 − , methanesulfonate (MSA), NH 4 + ,210Pb, and7Be. At Mawson for which we have a multiple year data set, the annual mean concentration of each species sometimes vary significantly from one year to the next: Na+, 68–151 ng m−3; NO 3 − , 25–30 ng m−3; nss SO 4 2− , 81–97 ng m−3; MSA, 19–28 ng m−3; NH 4 + , 16–21 ng m−3;210Pb, 0.75–0.86 fCi m−3. Results from multiple variable regression of non-sea-salt (nss) SO 4 2− with MSA and NO 3 − as the independent variables indicates that, at Mawson, the nss SO 4 2− /MSA ratio resulting from the oxidation of dimethylsulfide (DMS) is 2.80±0.13, about 13% lower than our earlier estimate (3.22) that was based on 2.5 years of data. A similar analysis indicates that the ratio at Palmer is about 40% lower, 1.71±0.10, and more comparable to previous results over the southern oceans. These results when combined with previously published data suggest that the differences in the ratio may reflect a more rapid loss of MSA relative to nss SO 4 2− during transport over Antarctica from the oceanic source region. The mean210Pb concentrations at Palmer and Marsh and the mean NO 3 − concentration at Palmer are about a factor of two lower than those at Mawson. The210Pb distributions are consistent with a210Pb minimum in the marine boundary layer in the region of 40°–60° S. These features and the similar seasonalities of NO 3 − and210Pb at Mawson support the conclusion that the primary source regions for NO 3 − are continental. In contrast, the mean concentrations of MSA, nss SO 4 2− , and NH 4 + at Palmer are all higher than those at Mawson: MSA by a factor of 2; nss SO 4 2− by 10%; and NH 4 + by more than 50%. However, the factor differences exhibit substantial seasonal variability; the largest differences generally occur during the austral summer when the concentrations of most of the species are highest. NH 4 + /(nss SO 4 2− +MSA) equivalent ratios indicate that NH3 neutralizes about 60% of the sulfur acids during December at both Mawson and Palmer, but only about 30% at Mawson during February and March.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of atmospheric chemistry 4 (1986), S. 227-240 
    ISSN: 1573-0662
    Keywords: Sulfur cycle ; marine atmosphere ; marine aerosols
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Concentrations of aerosol methanesulfonic acid (MSA) and non-sea-salt (nss) sulfate were measured at six island stations in the Pacific Ocean to investigate regional and seasonal patterns of organosulfur emissions and the origin of nss sulfate over the Pacific. The mean MSA concentrations, in μg/m3, at the stations were: Shemya, 0.097±0.098; Midway, 0.029±0.021; Fanning, 0.044±0.012; American Samoa, 0.026±0.012; New Caledonia, 0.021±0.009; Norfolk, 0.024±0.019. The extremely high MSA levels found at Shemya indicate a major source of organosulfur emissions in the western North Pacific. Significant seasonal trends in MSA were observed, with higher MSA occurring during warm months. The amplitude of the seasonal variation was greatest at higher latitude stations. At Fanning and American Samoa, which have minimal input of continental material, there is a significant positive correlation between MSA and nss sulfate. MSA/nss sulfate ratios at other Pacific stations exhibit greater variability, which may be related to variations in: the input of continentally derived sulfate, the composition of oceanic organosulfur emissions, and atmospheric reaction pathways.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1573-515X
    Keywords: dust ; deposition ; iron ; models ; NHx ; NOy ; nutrients
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Atmospheric chemical models are used to estimate the deposition rate of various inorganic oxides of nitrogen (NOy), reduced nitrogen species (NHx) and mineral dust to the North Atlantic Ocean (NAO). The estimated deposition of NOy to the NAO (excluding the coastal ocean) and the Caribbean is 360 × 109 Moles-N m−2 yr−1 (5.0 Tg N); this is equivalent to about 13% of the estimated global emission rate (natural and anthropogenic) and a quarter of the emission rate from sources in North America and Europe. In the case of NHx, 258 Moles-N m−2 yr−1 (3.6 Tg N) are deposited to the NAO and the Caribbean; this is about 6% of the global continental emissions. There is relatively little data on the deposition rate of organic nitrogen species; nonetheless, this evidence suggests that concentrations and deposition rates are comparable to those for inorganic nitrogen. Because of anthropogenic emissions, the present-day deposition rate of NOy to the NAO is about five times greater than pre-industrial times largely due to emissions from energy production and biomass burning. The present-day emissions of NHx from continental anthropogenic sources are about four-to-five times greater than natural sources, mostly due to the impact of emissions from animal wastes associated with food production. Indeed, present-day emissions of NHx from animal waste are estimated to be about 10 times greater than the pre-human era. The deposition rate of mineral dust to the NAO is about 170 Tg yr−1; deposited with the dust (assuming average crustal abundances) is about 6 Tg yr−1 of Fe and 0.2 Tg yr−1 of P. Dust deposition in the NAO is almost completely attributable to transport from North African sources; a substantial fraction of the dust over the NAO is probably mobilized as a consequence of land use practices in arid regions and, consequently, it should be regarded as a pollutant.
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