ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    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.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1573-0662
    Keywords: Antarctica ; aerosol particles ; ice ; biogeochemical cycles ; sulfate ; nitrate ; methanesulfonate ; lcad-210 ; boryllium-7 ; sea-salt
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract High volume aerosol samples were collected continuously at Mawson, Antarctica (67°36'S, 62°30'E), from February 1987 through October 1989. All samples were analyzed for Na+, Cl-, SO4 =, NO3 -, methanesulfonate (MSA), NH4 +,7Be, and210Pb. The annual mean concentrations of many of the species are very low, substantially lower than even those over the relatively pristine regions of the tropical and subtropical South Pacific. The concentrations at Mawson are comparable both in magnitude and in seasonality to those which have been measured in long term studies at the South Pole and at the coastal German Antarctic research station, Georg von Neumayer (GvN). This comparability suggests that the aerosol composition may be relatively uniform over a broad sector of the Antarctic. The concentrations of most of the species exhibit very strong and sharply-defined seasonal cycles. MSA, non-sea-salt (nss) SO4 = and NH4 + all exhibit similar cycles, with maxima during the austral summer (December through February) being more than an order of magnitude higher than the winter minima. The limited7Be data appears to exhibit a similar cycle. Although nitrate and210Pb also exhibit relatively high concentrations during the austral summer, their cycles are far more complex than those of the previous species with indications of multiple peaks. As expected, the concentration of sea-salt (as indicated by Na+ and Cl-) peaks during the winter. The results from multiple variable regression analyses indicate that the dominant source of nss SO4 = is the oxidation of dimethylsulfide (DMS) which produces MSA and nss SO4 = in a ratio of about 0.31 (about five times higher than that over the tropical and subtropical oceans). However, a very significant fraction (about 25%) of the nss SO4 = is associated with NO3 -, The seasonal cycle of NO3 - is similar to that of210Pb and distinctly different from that of7Be and MSA. These results indicate that the major source of NO3 - over Antarctica is probably continental as opposed to stratospheric or marine biogenic.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 1573-0662
    Keywords: Acrosol particles ; mineral acrosol ; antimony ; selenium ; non-sea salt sulfate ; biogeochemical cycles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The concentrations of selected trace elements and non-sea salt sulfate were determined for aerosol particle samples collected over the open North Atlantic Ocean as part of the Atmosphere/Ocean Chemistry Experiment (AEROCE). The concentrations of atmospheric sea salt and mineral aerosol, which together dominate the mass of particulate material in the atmosphere, were higher at Barbados than at Bermuda. In contrast, the impact of pollution sources on trace element concentrations was more evident at Bermuda than at Barbados. At both sites Sb and Se were enriched significantly over the concentrations expected from mineral dust or from atmospheric sea salt. Moreover, the concentrations of Sb and Se were correlated, and the observed Sb/Se ratios often were similar to those resulting from anthropogenic emissions. At Bermuda, the concentrations of Sb and Se co-varied with non-sea salt sulfate, suggesting that a significant fraction of the non-sea salt sulfate is anthropogenic. In a broader context, the synthesis of results demonstrates that trace element data are useful for evaluating the relative contributions of anthropogenic vs. natural sources to the budgets of non-sea salt sulfate in acrosol particles.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...