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 33 resources
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Icebergs and sea ice rework the sediments of high-latitude shelves, producing modern diamicts (ice-keel turbates) unrelated to glacial proximity. Off Antarctica, sidescan sonar data indicate the presence of ice-gouge features formed by the physical interaction between ice keels and the sea bed. These are recognized as incisions a few metres deep and tens of metres wide, in water depths up to 500 m. On the submarine bank tops and slopes off Wilkes Land and in the Weddell Sea, subcircular depressions 30 to 150 m in diameter, a washboard pattern, and hummocky bed features also represent iceberg-resting sites. The freshness of sea-bed morphology, nearby Holocene sediment ponding, and active hydraulic sedimentary processes indicate that the sea floor is being reworked by iceberg keels. Tabular iceberg drafts in excess of 330 m have been measured, and modeling studies suggest that nontabular iceberg drafts of 500 m are possible. We conclude that a modern ice-keel turbate deposit in the form of a poorly stratified diamicton is probably widespread on that part (54%) of the Antarctic shelf less than 500 m deep.
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Electrophoretic analyses of allele distributions at nine polymorphic gene loci were conducted in samples of Euphausia superba from the Bransfield Strait, off the South Orkney Islands, and from the south-eastern part of the Weddell Sea. The aim was to determine whether reported phenotypic differences between krill stocks from these areas could be linked to genotypic differences. Despite minor deviations of genotype distributions from Hardy-Weinberg expectations, the data gave no evidence of genetic heterogeneity over the sampled area, and the hypothesis of a single genetically homogeneous krill population could not be rejected. Genetic data for four selected loci were verified by using two different electrophoretic methods. Results from these two techniques yielded no discrepancies in interpretation of the data.
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The Southern Ocean circulation and sea-ice distribution is briefly described. The formation of extremely cold bottom water in the Weddell Sea and its relation to the floating Ronne-Filchner Ice Shelves is discussed. It is shown that a concentrated swift eroding bottom current with anomalous low ratio transports the cold and dense ice Shelf Water from the shelf towards large depths. Comments are made on possible implications of this process for the large-scale deep-water circulation and for the interpretation of sediment cores.
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A prominent escarpment, called the Explora-Andenes Escarpment, has been recognized between long. 40°W, lat. 72°40^primeS and long. 10°W, lat. 69°20^primeS. It separates the continental margin from the Weddell Sea basin. Our recent MCS data have revealed the presence of some remarkably symmetric structures beneath a thick pile of tectonically undisturbed sediments. For example, two extensive wedge-shaped basement units occur between 20°W and 40°W. These units are characterized by a pattern of divergent reflectors which surround an elongated depression in basement. The northern wedge terminates against the Explora-Andenes Escarpment between 25°W and 30°W. The southern wedge, known as the Explora Wedge, shows a northward-dipping reflection pattern. The seismic characteristics suggest that both wedges consist of volcanic rocks. The basement depression is interpreted as a failed rift basin. The initial fragmentation of Gondwana was accompanied by prolific volcanism, which led to the emplacement of the wedges of "dipping reflectors." The tectonomagmatic/volcanic period was followed by transtensional movements between Africa and Antarctica. This phase was heralded by the formation of the Explora-Andenes Escarpment as a new plate boundary and the opening of the Weddell Sea by sea-floor spreading. The Explora-Andenes Escarpment cuts across the early rift structures. The initial fragmentation of Gondwana was accompanied by prolific volcanism, which led to the emplacement of the wedges of dipping reflectors. The tectonomagmatic/volcanic period was followed by transtensional movements between Africa and Antarctica. This phase was heralded by the formation of the Explora-Andenes Escarpment as a new plate boundary and the opening of the Weddell Sea by sea-floor spreading. The Explora-Andenes Escarpment cuts across the early rift structures.
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Nine samples of Antarctic krill collected at seven localities in the Palmer Archipelago and Bransfield Strait west of the Antarctic Peninsula were analysed for genetic variation at eight enzyme loci. Despite significant among sample heterogeneity in allele frequencies, no convincing evidence was found to support the hypothesis of distinct genetic stocks of Euphausia superba in the investigated area. Allele frequency distributions could not be correlated to regional differences in size patterns. Allelic proportions at the PGI locus did not indicate that the investigated krill was genetically different from E. superba from the Weddell Sea region (from earlier investigations). Deviations of genotypes, or allele frequencies from those expected under Hardy-Weinberg equilibrium, however, may indicate regional, or yearly variation due to occasional selection.
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An improved Gondwanaland reconstruction compatible with geological and geophysical information from the surrounding oceans and continents seems to require microplates to solve the enigmatic pre-early-Mesozoic tectonic relation between West and East Antarctica1. New multi-channel seismic reflection data from the southeastern Weddell Sea acquired during the 1984–85 Norwegian Antarctic Research Expedition (NARE) have outlined a linear WSW–ENE-trending basement ridge buried below the continental slope over a distance of 700 km. This structural high truncates the trend of the large sedimentary basins below the Filchner and Ronne ice shelves and may continue to within a few hundred kilometres of the Antarctic Penninsula. We interpret the basement ridge as part of the East Antarctic plate boundary during the break-up of Gondwana. The morphology and structure of this boundary show greater apparent similarity to a rifted or obliquely rifted margin than to the sheared margin which is predicted by current reconstructions2,3. A linear East Antarctic plate margin extending to the vicinity of the Antarctic Peninsula makes any post-rift micro-plate motion in the Weddell Embayment unlikely.
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In the austral summer of 1983, schools of krill from Bransfield Strait and Palmer Archipelago were analyzed for composition in terms of size frequencies and maturity stages. Juveniles dominated in all schools, and mature animals never exceeded 6.8% of the animals at any sampling site. Gravid females were encountered in only four out of 15 schools and were never more frequent than 1.8% of the animals in any school. Among subadults and juveniles the largest animals were found on the inside of Palmer Archipelago. Smaller nonreproductive animals were on the outside and in Bransfield Strait. A second group of juveniles, in a size range of 12-15 mm, was more pronounced north of Crocker Passage than south of the Passage. Their potential origin from a more slowly growing and later spawning Southern Weddell Sea population is discussed. Lack of reproductive animals in the Bransfield/South Shetlands vicinity may reflect yearly variation in this region. A hypothesis is put forward on the basis of this study that Palmer Archipelago is a nursery ground for krill spawned elsewhere. The sites of origin of this krill could be ascertained on the basis of studies of enzyme polymorphism in these populations.
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