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 6 resources
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We present the first detailed maps of fast ice around East Antarctica (75°E–170°E), using an image correlation technique applied to RADARSAT ScanSAR images from November in 1997 and 1999. This method is based upon searching for, and distinguishing, correlated regions of the ice-covered ocean which remain stationary, in contrast to adjacent moving pack ice. Within the overlapping longitudinal range of ∼86°E–150.6°E, the total fast-ice area is 141,450 km2 in 1997 and 152,216 km2 in 1999. Calibrated radar backscatter data are also used to determine the distribution of two fast-ice classes based on their surface roughness characteristics. These are “smooth” fast ice (−25.4 dB to −13.5 dB) and “rough” fast ice (−13.5 dB to −2.5 dB). The former comprises ∼67% of the total area, with rough fast ice making up the remaining ∼33%. An estimate is made of fast-ice volume, on the basis of fast-ice type as a proxy measure of ice thickness and area. Results suggest that although fast ice forms 2–16% of the total November sea ice area for this sector of East Antarctica in 1997 and 1999 (average 8.3% across maps), it may comprise 6–57% of the total ice volume (average ∼28% across maps). Grounded icebergs play a key role in fast-ice distribution in all regions apart from 150°E–170°E. These are “snapshot” estimates only, and more work is required to determine longer-term spatiotemporal variability.
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It is shown by use of a newly discovered, old photo of the missing type that Siphulina orphnina (Hue) C. W. Dodge is identical with Pannaria caespitosa P. M. Jorg. The new combination Pannaria orphnina (Hue) R M. Jorg. is made, and the name neotypitied. Parmeliella austroshetlandica Sochting & Ovstedal is shown to be a species in the small subantarctic genus Peltularia R. Sant. (Coccocarpiaceae), and is transferred to that genus.
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The climatic features of Antarctic waters are more extreme and constant than in the Arctic. The Antarctic has been isolated and cold longer than the Arctic. The polar ichthyofaunas differ in age, endemism, taxonomy, zoogeographic distinctiveness and physiological tolerance to environmental parameters. The Arctic is the connection between the Antarctic and the temperate-tropical systems. Paradigmatic comparisons of the pathways of adaptive evolution of fish from both poles address the oxygen-transport system and the antifreezes of northern and southern species, (i) Haemoglobin evolution has included adaptations at the biochemical, physiological and molecular levels. Within the study of the molecular bases offish cold adaptation, and taking advantage of the information on haemoglobin amino acid sequence, we analysed the evolutionary history of the ? and ? globins of Antarctic, Arctic and temperate haemoglobins as a basis for reconstructing phylogenetic relationships. In the trees, the constant physico-chemical conditions of the Antarctic waters are matched by clear grouping of globin sequences, whereas the variability typical of the Arctic ecosystem corresponds to high sequence variation, reflected by scattered intermediate positions between the Antarctic and non-Antarctic clades. (ii) Antifreeze (glyco)proteins and peptides allow polar fish to survive at sub-zero temperatures. In Antarctic Notothenioidei the antifreeze gene evolved from a trypsinogen-like serine protease gene. In the Arctic polar cod the genome contains genes which encode nearly identical proteins, but have evolved from a different genomic locus–a case of convergent evolution.
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