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 1,176 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 programme of systematic iceberg observations was initiated in 1981 by Norsk Polarinstitutt through the SCAR Working Group on Glaciology. Icebergs are recorded every 6 h and in five length groups: 10-50, 50-200, 200-500 and 500-1000 m, and those over 1000 m, which are described individually. Data on more than 100 000 icebergs are now on file at Norsk Polarinstitutt, and practically all ships travelling to and from Antarctica participate in the collection of data. This paper presents the first comprehensive analysis of the iceberg data. The quality of the data set is discussed, with consideration of potential errors in and limitations of the data, and various statistical evaluations. Representative distribution data are presented, and used to determine iceberg production, disintegration and mean residence times, and regional and total Antarctic calving rates. The incidence of large-scale calving in particular is evaluated, including the remarkably large break-offs in recent years. These exceed both the total annual accumulation on the Antarctic continent and the mean annual calving rate as determined from ship observations. The results show further: (1) that there are more than 200 000 icebergs south of the Antarctic Convergence, (2) that there are large regional differences in iceberg calving rates and iceberg sizes, and (3) that the calving rate from Antarctica is higher than that given in most previous estimates, which implies (4) that the mass balance of the Antarctic ice sheet is not positive as suggested by most recent estimates.
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1. Autoproteolysis post mortem was examined at 0 degree C by following the changes in the major classes of krill (Euphausia superba and Euphausia crystallorophias) proteins and by liberation of peptides and free amino acids, and was based on experiments conducted on board expedition vessels in the Antarctic. 2. Primarily salt-soluble proteins were broken down during the first week of incubation, whereas water-soluble and insoluble proteins were degraded to a much smaller extent. The enzymes responsible for the hydrolysis presumably originate primarily from the digestive apparatus of the krill. 3. In general, the individual amino acids were released at rates corresponding to their relative occurrence in the bulk protein of the krill. Alanine was liberated in larger amounts than would be expected from the composition of the krill protein, and was evidently formed also by reactions other than proteolysis. Glutamic acid, and certain amino acids which presumably occur with high frequency adjacent to glumatic acid residues in the krill protein, were liberated only to a limited extent, and accumulated in smaller peptides. 4. During proteolysis, arginine seemed to be converted to some degree into ornithine, and on prolonged incubation conversion of arginine and lysine into their corresponding decarboxylation products, agmatine and cadaverine, appeared to take place.
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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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A systematic programme of side-scan sonar and plumb- line soundings was carried out in the Weddell Sea area in 1985 to measure the under-water sides of ice shelves and icebergs. From these observations the following model is suggested for the evolution of the ice front: (1) Initial stage: fracturing of the ice shelves takes place along smooth, curvi-linear segments with vertical faces. (2) Formative stage: the freshly formed vertical face is eroded both by wave and swell action around the water line, by small calvings from the undercut, overhanging subaerial face, and by submarine melting. The melting has a minimum at 50–100 m depth, and increases with depth to a rate of around 10 m a−1 at 200 m, This is about twice the rate of erosion at the water line. The variation in melting with depth results from a combination of summer melting by near-surface water, and year-round melting by water masses that are increasingly warmer than the pressure melting-point with depth. (3) Mature stage: this stage is reached after a few years of exposure. The backward erosion of the face leads to a shape with a prominent under-water “nose” with a maximum projection to more than 50 m at 50–100 m depth. The ramp above this slopes upwards to meet the vertical wall about 5 m below the water line. The ice below the nose is melted back beyond the above-water face. There is no net buoyancy and ice shelves at this mature stage are generally not up-warped at the front.
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Relatively little data on the distribution of Antarctic icebergs were available prior to 1980. The published literature included size data of about 5000 icebergs, and position data of 12 000 icebergs. There were indications that the size data were biased in favour of larger icebergs. A programme of systematic iceberg observations was therefore initiated by Norsk Polarinstitutt in 198! through the SCAR Working Group on Glaciology. This programme is based on standard “blue” forms distributed to all ships going to Antarctica. The icebergs are recorded every 6 h and in Five length groups: 10–50, 50–200, 200–500, and 500–1000 m, and those over 1000 m are described individually. The amount of data has increased greatly from the start in 1981–82. The position of 70 000 icebergs, including 50 000 that had been size classified, were on file at Norsk Polarinstitutt by December 1985, and the data set is growing rapidly. Most ships travelling to and from Antarctica now participate in collection of the data. ( shows the locations of the icebergs sighted.) Fig. 1. Location of iceberg observations under the programme initiated in 1981. Main ship tracks are clearly reflected. The average observation represents 14 icebergs. The size distribution of the classified icebergs observed under this programme up to December 1985 is given in : Table I The “standard size” (length, width, and thickness) is based on our observations from three Antarctic expeditions which carried out dedicated iceberg studies. Many icebergs are of course not right-angled parallelepipedal in shape, but this is a good approximation for most of the larger icebergs. The data are based both on visual sightings and on radar observations. Duplicate observations from a ship moving at slow or zero speed are as far as possible eliminated, both during observation, and by critical appraisal before the data are filed. The data editing also includes evaluation of data quality, especially in connection with radar observations, and comparison of positions and dimensions of the large icebergs in order to reduce to a minimum repeated observations from different vessels of icebergs >1000 m. These account for most of the iceberg mass (see ). Consideration of iceberg-distribution patterns and the observed area of the Southern Ocean, and of duplicate observations, indicates more than 300 000 icebergs south of the Antarctic Convergence, with a total ice mass of about 1016 kg. Consideration of mean residence times indicates an annual iceberg production from the continent of 23–1015 kg, which is considerably higher than most other recent estimates. This also suggests that the Antarctic ice sheet is in balance. The data indicate large regional differences in iceberg sizes, the most noticeable being between the two sides of the Antarctic Peninsula, and between the Amery Ice Shelf/ Prydz Bay area and the remainder of East Antarctica. These differences are probably mainly related to different calving sites. About one-third of the observed icebergs are over the continental shelf of Antarctica. The total under-water area of these icebergs is two orders of magnitude less than the under-water area of the Antarctic ice shelves. The annual total iceberg melting and its effect on the water masses over the continental shelf has been calculated from ocean-water temperature variations at 200 m depth and estimated melt rates. This turns out to be an order of magnitude less than the annual effect of melting sea ice. The iceberg data considered here are probably under-represented with respect to the smallest sizes, and they do not include icebergs that have become <10 m. Inclusion of these ice bodies would increase the total melt.
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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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The Antarctic krill (Euphausia superba) possesses an ‘over-dimensioned’ digestive system, which is of vital importance for the survival of this euphaucean shrimp in the extreme marine environment. The isolated enzymes contain a well-balanced mixture of both endo- and exopeptidases, assuring fast and complete breakdown of proteinaceous material. These unique properties have now been shown to be extremely valuable for the effective removal of necrotic debris, fibrin or blood crusts in vitro. Therefore the krill enzymes should be considered as an important resource in the future management of necrotic wounds.
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