Antarktis-bibliografi er en database over den norske Antarktis-litteraturen.
Hensikten med bibliografien er å synliggjøre norsk antarktisforskning og annen virksomhet/historie i det ekstreme sør. Bibliografien er ikke komplett, spesielt ikke for nyere forskning, men den blir oppdatert.
Norsk er her definert som minst én norsk forfatter, publikasjonssted Norge eller publikasjon som har utspring i norsk forskningsprosjekt.
Antarktis er her definert som alt sør for 60 grader. I tillegg har vi tatt med Bouvetøya.
Det er ingen avgrensing på språk (men det meste av innholdet er på norsk eller engelsk). Eldre norske antarktispublikasjoner (den eldste er fra 1894) er dominert av kvalfangst og ekspedisjoner. I nyere tid er det den internasjonale polarforskninga som dominerer. Bibliografien er tverrfaglig; den dekker både naturvitenskapene, politikk, historie osv. Skjønnlitteratur er også inkludert, men ikke avisartikler eller upublisert materiale.
Til høyre finner du en «HELP-knapp» for informasjon om søkemulighetene i databasen. Mange referanser har lett synlige lenker til fulltekstversjon av det aktuelle dokumentet. For de fleste tidsskriftartiklene er det også lagt inn sammendrag.
Bibliografien er produsert ved Norsk Polarinstitutts bibliotek.
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Results 4 resources
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Levels of persistent organic pollutants (POPs), such as polychlorinated biphenyls and pesticides have been determined in ambient air at Signy Island, Antarctica, over a period of 17 weeks. Mean concentrations for single polychlorinated biphenyls (0.02–17 pg/m3), for chlordanes (0.04–0.9 pg/m3), DDT compounds (0.07–0.40 pg/m3) and γ-hexachlorocyclohexane (HCH, 22 pg/m3) were comparable to those in Arctic air. However, α-HCH levels were approximately one order of magnitude lower. Compared to the Arctic, differences were also observed in the concentration ratios of α-/γ-HCH and chlordane compounds. Two possible atmospheric long-range transport episodes from South America were found by comparing 10-day back trajectories with observed concentration changes. The lower limits of determination (LOD) were mainly governed by the field blanks. They were satisfactory for the most volatile PCBs. However, many concentrations for DDT and chlordane compounds were below the LODs (range 0.1–1 pg/m3) or even the instrumental detection limit (0.01–0.03 pg/m3).
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A first long-term monitoring of selected persistent organic pollutants (POPs) in Antarctic air has been conducted at the Norwegian research station Troll (Dronning Maud Land). As target contaminants 32 PCB congeners, α- and γ-hexachlorocyclohexane (HCH), trans- and cis-chlordane, trans- and cis-nonachlor, p,p'- and o,p-DDT, DDD, DDE as well as hexachlorobenzene (HCB) were selected. The monitoring program with weekly samples taken during the period 2007–2010 was coordinated with the parallel program at the Norwegian Arctic monitoring site (Zeppelin mountain, Ny-Ålesund, Svalbard) in terms of priority compounds, sampling schedule as well as analytical methods. The POP concentration levels found in Antarctica were considerably lower than Arctic atmospheric background concentrations. Similar to observations for Arctic samples, HCB is the predominant POP compound, with levels of around 22 pg m−3 throughout the entire monitoring period. In general, the following concentration distribution was found for the Troll samples analyzed: HCB > Sum HCH > Sum PCB > Sum DDT > Sum chlordanes. Atmospheric long-range transport was identified as a major contamination source for POPs in Antarctic environments. Several long-range transport events with elevated levels of pesticides and/or compounds with industrial sources were identified based on retroplume calculations with a Lagrangian particle dispersion model (FLEXPART).
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The Troll Atmospheric Station in Antarctica (72°01'S, 2°32'E, 1309 m a.s.l.) was established and put into operation in early 2007. The main foci of the measurement programme are pollution and aerosols in the transition zone between the coastal zone and the inland ice plateau, complementing existing observation programmes along the Antarctic coast and on the Antarctic Plateau. After one year of operation, the monitoring programme is fully operative, and a comprehensive set of data is being analysed. As far as comparable data are available, there is satisfactory agreement between previous and new data. Both aerosol data and measurements of pollution indicate the episodic influence of coastal air masses throughout the year. Background values of medium long-lived pollutants such as CO, O3 and Hg are up to 50% lower than at corresponding Arctic sites (depending on the season), but are still significant. Total ozone and UV doses manifest the recurring Antarctic stratospheric ozone hole, which was moderately severe, but very persistent in 2007. Specific episodes of elevated aerosol concentration and mercury activation are currently under detailed investigation, and will be published separately.
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Spatial variations of atmospheric alkylated polycyclic aromatic hydrocarbons (Alk-PAHs) are key to understanding their long-range atmospheric transport (LRAT). However, limited Alk-PAHs data have hindered their LRAT characterizations on a global scale. In this study, 49 Alk-PAHs were measured in the atmospheric samples collected across the Western Pacific to the Southern Ocean. The summed concentration of 39 frequently detected Alk-PAHs (Σ39Alk-PAHs) was 25.8 ± 25.3 ng m–3. The concentrations of Σ39Alk-PAHs significantly declined with the decrease in latitude (°N). Higher concentrations (55.8 ± 33.8 ng m–3) were linked to continental air mass compared to oceanic/Antarctica air mass (17.0 ± 13.6 ng m–3), highlighting continental emissions as the primary source of marine atmospheric Alk-PAHs. An unexpected increase in the G/P partitioning ratio (KP) was found in samples farther away from the continent, which cannot be explained by the influence of temperature on the partitioning process. Deposition analysis suggested that gaseous concentrations and the G/P partitioning largely influenced deposition patterns. Hypothetical scenario analysis indicated that increased KP under snowy conditions could enhance the total Alk-PAH deposition. These findings emphasize the need for accurate characterization of partitioning and deposition processes when studying the global fate of Alk-PAHs, particularly in remote and polar regions.
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