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 20 resources
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We present the first data on attendance patterns, at-sea movements and diving behaviour of Antarctic fur seals breeding at Bouvetøya (Bouvet Island), Southern Ocean. While other colonies have been extensively studied, this remote and second largest global population remains relatively unknown. Time depth recorders and satellite relay data loggers were deployed on breeding females during the 2000–2001 and 2001–2002 summers. Attendance and foraging patterns were similar to those observed at colonies in the Scotia Sea region where Antarctic krill is the predominant prey. Early to mid-lactation trips ranged within ~100 km of the island, usually towards the west. The dominant direction shifted later in the season and the range also increased markedly to a peak between early February and early March. Solar elevation influenced arrivals and departures from the island, with most departures occurring around sunset. Diurnal variations in diving behaviour were consistent with the vertical migration of krill. Diving frequency was higher at night and diving effort peaked around morning twilight. Afternoon deep diving was common, suggesting that females might target dense daytime krill aggregations between the photic zone and the thermocline. Trip durations increased throughout early to mid-lactation, peaking in late January to early March, before again decreasing towards the end of lactation. Our results illustrate the substantial variability, both between individuals and within individuals over time, that is likely to reflect variations in prey distribution and in the growth requirements of pups. Such variations need to be taken into account when estimating habitat use and resource utilisation in marine top predators.
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Miniature electronic data recorders and transmitters have revolutionized the way we study animals over the past decades, particularly marine animals at sea. But, very recently, animal-borne instruments have also been designed and implemented that provide in situ hydrographic data from parts of the oceans where little or no other data are currently available (even from beneath the ice in polar regions). Ocean data is delivered from animal-borne instruments via satellites in near real-time, which would enrich the Global Ocean Observing System if animal-borne instruments were deployed systematically. In the last 10 years, studies involving more than 10 countries (Australia, Brazil, Canada, France, Germany, Greenland, Norway, South Africa, UK, USA) have demonstrated how highly accurate oceanographic sensors, integrated into standard animal, biologging instruments, can provide data of equal or better quality than XBT/XCTD data. Here, we present some of the pioneering studies and demonstrate that we now have enough information for many marine species to predict where they will go – within reasonable limits. Thus, we can direct sampling effort to particularly interesting and productive regions and maximize data return. In the future, biologging could certainly play an important part in the Global Ocean Observing System, by providing complementary data to more traditional sampling technologies - especially in the high latitudes. This paper will make a core contribution to the Plenary Sessions 4A, 4B and 5A and will be relevant to 2A, 2B and 3A.
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In recent years, the international “Southern Elephant seals as Oceanographic Samplers” (SEaOS) project has deployed miniaturized conductivity-temperature-depth satellite-relayed data loggers (CTD-SRDL) on elephant seals 1) to study their winter foraging ecology in relation to oceanographic conditions, and 2) to collect hydrographic data from polar regions, which are otherwise sparsely sampled. We summarize here the main results that have been published in both science components since 2003/2004. Instrumented southern elephant seals visit different regions within the Southern Ocean (frontal zones, continental shelf, and/or ice covered areas) and forage in a variety of different water masses (e.g. Circumpolar Deep Water upwelling regions, High Salinity Shelf Water), depending on their geographic distribution. Adult females and juvenile males from Kerguelen Is. forage pelagically in frontal zones of the Southern Indian Ocean, while adult males forage benthically over the Kerguelen Plateau and the Antarctic Continental Shelf, with the two groups feeding at different trophic levels as shown by stable isotopes analysis. Oceanographic studies using the data collected from the seals have, to date, concentrated on circumpolar and regional studies of the Antarctic Circumpolar Current (ACC) circulation. The temperature and salinity profiles documented by elephant seals at high latitudes, including below sea ice, have permitted quasi-circumpolar mapping of the southernmost fronts of the ACC. By merging conventional data and the high temporal and spatial resolution data collected by seal-borne SRDLs, it has been possible to describe precisely 1) the large-scale features of the ACC in the South Atlantic and its variability; 2) the circulation pattern over the Kerguelen plateau, revealing that the poorly known Fawn Trough concentrates an important proportion of the ACC flow in that region. Seals that foraged in ice covered areas have made eulerian time series available that have allowed for the estimation of sea ice formation rates, a parameter that is otherwise difficult to obtain, while also providing a unique description of the wintertime ocean circulation over the central Weddell Sea continental shelf. Finally, we present the first data collected by a newly-developed fluorescence sensor that as been embedded in the regular CTD-SRDL and deployed on elephant seals at Kerguelen. The fluorometer data obtained have offered the first synoptic view of the 3 dimensional distribution of temperature, salinity and fluorescence over a vast sector of the Southern Indian Ocean, allowing us to describe both vertical and horizontal variations in chlorophyll. This paper will make a core contribution to the Plenary Sessions 2C, 3A and 4A, and will be relevant to 2A and 2B.
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Entanglements of Antarctic fur seals Arctocephalus gazella were recorded during four summers from 1996 to 2002 at the subantarctic island, Bouvetøya. Rates of entanglement varied between 0.024% and 0.059%. These rates are low for a pinniped population and might be because of the geographic isolation of the haulout site. An apparent decrease in the levels of entanglement over the course of the study was likely due, at least in part, to the removal of entanglements by observers. At least two-thirds of entangling materials were generated by fishery sources. Since there is no known local source of anthropogenic marine pollution, seals become entangled either in waters distant from the island, or when materials drift into local waters. Significantly more subadults were found entangled than expected from the postulated population age class distribution.
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Antarctic fur seal Arctocephalus gazella pup production at Nyrøysa, Bouvetøya was estimated to be approximately 15,000 per annum during each of four summers from 1996 to 2002, indicating a total population of about 66,000. While the Bouvetøya population is the second largest for this species, pup production at this site still accounts for only 2.4% of the global total. This population experienced a mean annual rate of increase of 30.6% for the period 1989–1996, perhaps due, in part, to significant immigration, but has been stable since 1996. Historical accounts of significant numbers of animals being present towards the end of the period of sealing (C.1800–1930), indicate that the geographic isolation and inaccessibility of this site may have resulted in the Bouvetøya population being one of three populations that survived a series of periods of extreme exploitation of this species.
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The distribution and speciation of iron was determined along a transect in the eastern Atlantic sector (6°E) of the Southern Ocean during a collaborative Scandinavian/South African Antarctic cruise conducted in late austral summer (December 1997/January 1998). Elevated concentrations of dissolved iron (>0.4nM) were found at 60°S in the vicinity of the Spring Ice Edge (SIE) in tandem with a phytoplankton bloom, chiefly dominated by Phaeocystis sp. This bloom had developed rapidly after the loss of the seasonal sea ice cover. The iron that fuelled this bloom was mostly likely derived from sea ice melt. In the Winter Ice Edge (WIE), around 55°S, dissolved iron concentrations were low (<0.2nM) and corresponded to lower biological productivity, biomass. In the Antarctic Polar Front, at approximately 50°S, a vertical profile of dissolved iron showed low concentrations (<0.2nM); however, a surface survey showed higher concentrations (1–3nM), and considerable patchiness in this dynamic frontal region. The chemical speciation of iron was dominated by organic complexation throughout the study region. Organic iron-complexing ligands ([L]) ranged from 0.9 to 3.0nM Fe equivalents, with complex stability logKFeL′=21.4–23.5. Estimated concentrations of inorganic iron (Fe′) ranged from 0.03 to 0.79pM, with the highest values found in the Phaeocystis bloom in the SIE. A vertical profile of iron-complexing ligands in the WIE showed a maximum consistent with a biological source for ligand production and near surface minimum possibly consistent with loss via photodecomposition. This work further confirms the role iron that has in the Southern Ocean in limiting primary productivity.
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Southern elephant seals were counted and classified into subjective sex-age classes on a weekly basis during expeditions to Bouvet Island in the austral summers of 1996/1997 and 1998/1999. The expeditions coincided with the moulting period of elephant seals aged one year and older. The presence of weaned pups at the principal haulout site, Nyrøysa/Westwindstranda, during the latter expedition, indicates that breeding took place here during 1998. Elephant seal counts from previous expeditions are summarised.
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Collection and analysis of natural regurgitations and fresh scats, deposited by Antarctic fur seals at the Nyrøysa colony, Bouvetøya, during December 1998 to February 1999, afforded a comprehensive description of the dietary composition of this expanding population during the summer months. Mature, adult Euphausia superba was the staple diet of fur seals at Nyrøysa, while squid and myctophid fish appeared to be taken opportunistically. In metric tons, the total Bouvetøya fur seal population is estimated to have consumed a minimum of 14,365 t krill (representing 1.2713 × 1010 individuals of 1.13 g mass), 186 t fish, 184 t squid and 14,735 t over 3 months, but there are many possible sources of error in these estimates. It is presumed that over-indulgence in krill may cause animals to regurgitate ashore.
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Abstract Commercial sealing in the 18th and 19th centuries had a major impact on the Antarctic and subantarctic fur seal populations (Arctocephalus gazella and A. tropicalis) in the Southern Ocean. The intensive and unrestricted nature of the industry ensured substantial reductions in population sizes and resulted in both species becoming locally extinct at some sites. However, both species are continuing to recover, through the recolonization of islands across their former range and increasing population size. This study investigated the extent and pattern of genetic variation in each species to examine the hypothesis that higher levels of historic sealing in A. gazella have resulted in a greater loss of genetic variability and population structure compared with A. tropicalis. A 316-bp section of the mitochondrial control region was sequenced and revealed nucleotide diversities of 3.2% and 4.8% for A. gazella and A. tropicalis, respectively. There was no geographical distribution of lineages observed within either species, although the respective ΦST values of 0.074 and 0.19 were significantly greater than zero. These data indicate low levels of population structure in A. gazella and relatively high levels in A. tropicalis. Additional samples screened with restriction endonucleases were incorporated, and the distribution of restriction fragment length polymorphism (RFLP) and sequence haplotypes were examined to identify the main source populations of newly recolonized islands. For A. tropicalis, the data suggest that Macquarie Island and Iles Crozet were probably recolonized by females from Marion Island, and to a lesser extent Ile Amsterdam. Although there was less population structure within A. gazella, there were two geographical regions identified: a western region containing the populations of South Georgia and Bouvet?ya, which were the probable sources for populations at Marion, the South Shetland and Heard Islands; and an eastern region containing the panmictic populations of Iles Kerguelen and Macquarie Island. The latter region may be a result of a pronounced founder effect, or represent a remnant population that survived sealing at Iles Kerguelen.
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