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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En rekelignende skapning i Sørishavet er Kjell Inge Røkkes nye yndling. Den kan nemlig brukes i alt fra slankemidler til fiskefôr. Men vet vi nok om krill til å slippe trålerne løs? Forskningsskipet G.O. Sars har vært på tokt for å finne u mer.
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Identification of DNA sequence diversity is a powerful means for assessing the species present in environmental samples. The most common molecular strategies for estimating taxonomic composition depend upon PCR with universal primers that amplify an orthologous DNA region from a range of species. The diversity of sequences within a sample that can be detected by universal primers is often compromised by high concentrations of some DNA templates. If the DNA within the sample contains a small number of sequences in relatively high concentrations, then less concentrated sequences are often not amplified because the PCR favours the dominant DNA types. This is a particular problem in molecular diet studies, where predator DNA is often present in great excess of food-derived DNA.
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Climate is altering rapidly in parts of the Arctic and Antarctic but we know little about how marine organisms are responding to, or might respond to such changes. Knowledge of within-taxon variability is the vital context (currently missing) to interpretation of environmental signals. We investigated growth in six species and three genera of erect Antarctic bryozoans, an ideal model taxon to investigate such response. Cellarinella margueritae, C. nodulata, C. rogickae, C. watersi, Melicerita obliqua and Stomhypselosaria watersi, extended 3.4, 5.2, 4.6, 4.1, 4.9 and 4.5 mm year(-1) and synthesised 24, 55, 45, 176, 34 and 46 mg CaCO3 year(-1), respectively. The maximum ages of these species ranged from 11 to 15 years except M. obliqua, which reached 32 years. This is the first investigation of growth rates of closely related Antarctic invertebrate species and reports the slowest growth rates of bryozoans known from anywhere to date. Our data coupled with that from literature shows that Antarctic bryozoan growth varies << 10(1) between species, 10(1) between genera, 10(2) between morphologies and is similar to 10(1) slower than in tropical or temperate regions. However, within encrusting types the slowest growing species grow at similar rates from poles to tropics. Age was a strong confounding factor across our Antarctic study species but age-standardised data showed a possible decline in annual growth from 1992 to 2003. We identify several factors increasing this environmental signal strength, including (1) the importance of generic (though not necessarily species) identification and (2) use of dry-mass or ash-free dry-mass as the measures of growth.
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Responses by marine top predators to environmental variability have previously been almost impossible to observe directly. By using animal-mounted instruments simultaneously recording movements, diving behavior, and in situ oceanographic properties, we studied the behavioral and physiological responses of southern elephant seals to spatial environmental variability throughout their circumpolar range. Improved body condition of seals in the Atlantic sector was associated with Circumpolar Deep Water upwelling regions within the Antarctic Circumpolar Current, whereas High-Salinity Shelf Waters or temperature/salinity gradients under winter pack ice were important in the Indian and Pacific sectors. Energetic consequences of these variations could help explain recently observed population trends, showing the usefulness of this approach in examining the sensitivity of top predators to global and regional-scale climate variability.
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Six out of ten adult Ross seals that were tagged with Argos satellite-linked dive recorders off Queen Maud Land, just after the moult in February, provided data on location and diving activity throughout a year. Shortly after tagging, the animals headed 2,000 km north and stayed pelagic in the area south of the Antarctic Polar Front, until October when they went south into the pack-ice. Throughout the year they made about 100 dives a day, most to a depth of 100–300 m, the deepest dive on record being 792 m, while some dives were very shallow during their stay in the pack-ice. Most dives, outside the breeding and moulting period, lasted for 5–15 min throughout the year. This diving behaviour is consistent with feeding on mid-water fish, like Pleurogramma antarcticum, squid, and to some extent krill (Euphausia superba), when in the pack-ice, and myctophid fish and several species of squid, when in the open ocean. The nursing period was 13 days in mid-November, and moulting occurs in late January–early February, which is the period when sightings surveys for this species should be done.
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We examined deep-sea benthic data on polychaetes, isopods and bivalves from the Atlantic sector of the Southern Ocean. Samples were taken during the expeditions EASIZ II (1998), ANDEEP I and II (2002) (depth: 742-6,348 m). The range between sites varies from 3 to 1,900 km. Polychaetes (175 species in total) and isopods (383 species) had a high proportion of species restricted to one or two sites (72 and 70%, respectively). Bivalves (46 species) had a higher proportion of species represented at more sites. Beta diversity (Whittaker and Jaccard) was higher for polychaetes and isopods than for bivalves. The impact of depth on species richness was not consistent among groups; polychaetes showed a negative relationship to depth, isopods displayed highest richness in the middle depth range (2,000-4,000 m), whereas bivalves showed no clear relationship to depth. Species richness was not related to latitude (58-74 degrees S) or longitude (22-60 degrees W) for any group.
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Macrobenthic soft-bottom molluscs were sampled in 30 stations located in the Bellingshausen Sea at depths ranging from 90 to 3304 m. The samples were collected using a quantitative grab box-corer during the cruises BENTART 03, from 24 January to 3 March 2003, and BENTART 06, from 2 January to 16 February 2006. Molluscs represent 1074 specimens belonging to 62 species of Polyplacophora, Gastropoda, Bivalvia and Scaphopoda. The bivalve Cyamiocardium denticulatum was the most abundant species (448 specimens). The abundance per station varied between 1 and 446 specimens. The Shannon–Wiener diversity index ranged between one specimen and 2.36, the Pielou evenness index ranged between 0.00 and 1 and species richness ranged from 1 to 14 species. Diversity showed great variations at different stations. After multivariate analysis (cluster analysis and nonmetrical multidimensional scaling) based on Bray–Curtis similarities, we were able to separate two principal clusters. The first cluster groups together species from shallower bottoms near Peter I Island and the Antarctic Peninsula, and the second cluster groups together species from deeper bottoms in the Bellingshausen Sea. The combination of environmental variables with the highest correlations with faunistic data was that of depth and coarse sand at the surface.
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This review concerns crustaceans that associate with sea ice. Particular emphasis is placed on comparing and contrasting the Arctic and Antarctic sea ice habitats, and the subsequent influence of these environments on the life history strategies of the crustacean fauna. Sea ice is the dominant feature of both polar marine ecosystems, playing a central role in physical processes and providing an essential habitat for organisms ranging in size from viruses to whales. Similarities between the Arctic and Antarctic marine ecosystems include variable cover of sea ice over an annual cycle, a light regimen that can extend from months of total darkness to months of continuous light and a pronounced seasonality in primary production. Although there are many similarities, there are also major differences between the two regions: The Antarctic experiences greater seasonal change in its sea ice extent, much of the ice is over very deep water and more than 80% breaks out each year. In contrast, Arctic sea ice often covers comparatively shallow water, doubles in its extent on an annual cycle and the ice may persist for several decades. Crustaceans, particularly copepods and amphipods, are abundant in the sea ice zone at both poles, either living within the brine channel system of the ice‐crystal matrix or inhabiting the ice–water interface. Many species associate with ice for only a part of their life cycle, while others appear entirely dependent upon it for reproduction and development. Although similarities exist between the two faunas, many differences are emerging. Most notable are the much higher abundance and biomass of Antarctic copepods, the dominance of the Antarctic sea ice copepod fauna by calanoids, the high euphausiid biomass in Southern Ocean waters and the lack of any species that appear fully dependent on the ice. In the Arctic, the ice‐associated fauna is dominated by amphipods. Calanoid copepods are not tightly associated with the ice, while harpacticoids and cyclopoids are abundant. Euphausiids are nearly absent from the high Arctic. Life history strategies are variable, although reproductive cycles and life spans are generally longer than those for temperate congeners. Species at both poles tend to be opportunistic feeders and periods of diapause or other reductions in metabolic expenditure are not uncommon.
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Our knowledge of the biodiversity of the Southern Ocean (SO) deep benthos is scarce. In this review, we describe the general biodiversity patterns of meio-, macro- and megafaunal taxa, based on historical and recent expeditions, and against the background of the geological events and phylogenetic relationships that have influenced the biodiversity and evolution of the investigated taxa. The relationship of the fauna to environmental parameters, such as water depth, sediment type, food availability and carbonate solubility, as well as species interrelationships, probably have shaped present-day biodiversity patterns as much as evolution. However, different taxa exhibit different large-scale biodiversity and biogeographic patterns. Moreover, there is rarely any clear relationship of biodiversity pattern with depth, latitude or environmental parameters, such as sediment composition or grain size. Similarities and differences between the SO biodiversity and biodiversity of global oceans are outlined. The high percentage (often more than 90%) of new species in almost all taxa, as well as the high degree of endemism of many groups, may reflect undersampling of the area, and it is likely to decrease as more information is gathered about SO deep-sea biodiversity by future expeditions. Indeed, among certain taxa such as the Foraminifera, close links at the species level are already apparent between deep Weddell Sea faunas and those from similar depths in the North Atlantic and Arctic. With regard to the vertical zonation from the shelf edge into deep water, biodiversity patterns among some taxa in the SO might differ from those in other deep-sea areas, due to the deep Antarctic shelf and the evolution of eurybathy in many species, as well as to deep-water production that can fuel the SO deep sea with freshly produced organic matter derived not only from phytoplankton, but also from ice algae.
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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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Diverse microbial communities survive within the sea ice matrix and are integral to the energy base of the Southern Ocean. Here we describe initial findings of a four season survey (between 1999–2004) of community structure and biomass of microalgae within the sea ice and in the underlying water column at Cape Evans and Cape Hallett, in the Ross Sea, Antarctica as part of the Latitudinal Gradient Project. At Cape Evans, bottom-ice chlorophyll a levels ranged from 4.4 to 173 mg Chl a m−2. Dominant species were Nitzschia stellata, N. lecointei, and Entomoneis kjellmanii, while the proportion of Berkeleya adeliensis increased steadily during spring. Despite being obtained later in the season, the Cape Hallett data show considerably lower standing stocks of chlorophyll ranging from 0.11 to 36.8 mg Chl a m−2. This difference was attributed to a strong current, which may have ablated much of the bottom ice biomass and provided biomass to the water below. This loss of algae from the bottom of the ice may explain why the ice community contributed only 2% of the standing stock in the total water column. Dominant species at Cape Hallett were Nitzschia stellata, Fragilariopsis curta and Cylindrotheca closterium. The low biomass at Cape Hallett and the prevalence of smaller-celled diatoms in the bottom ice community indicate that the ice here is more typical of pack ice than fast ice. Further data will allow us to quantify and model the extent to which ice-driven dynamics control the structure and function of the sea ice ecosystem and to assess its resilience to changing sea ice conditions.
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Polar shores probably represent the most dynamic and extremely disturbed environments on the globe. Nevertheless intense battles amongst sessile organisms for space are commonplace on hard substrata, mainly between fast-growing pioneer species. In this study we examined spatial interactions in encrusting species at 3 sites within each of 2 high Arctic localities, Horsundfjord (77°N) and Kongsfjord (79°N) in Spitsbergen, and 2 Antarctic localities, Signy Island (60°S) and Adelaide Island (68°S). In both polar regions 1 to 11% of encrusting fauna were involved in intraspecific interactions. Intraspecific competition was common; it usually involved just 1 or 2 pioneer species, mainly ended in tied outcomes, and most variability was at a local scale. The proportion of intraspecific encounters varied considerably at local (km) scales (19 to 99% intraspecific at different sites), reflecting an extremely patchy environment due to ice scour. Most intraspecific encounters resulted in ties (stand-offs) and again most variability was at a local scale. Many intraspecific encounters were constructive, forming large (>1 m3) foliaceous colonies (termed bioconstructions) whose 3D structures can harbour rich biotas. In other colonies intraspecific competition caused crowding and accelerated ovicell production (reproductive activity). Homosyndrome (fusion) was not observed in the Arctic and was rare in the Antarctic, where its frequency differed significantly between competitor identities. We found that the likelihood of meeting conspecifics versus other species and of tied outcomes in encounters was related to the performance of species in interspecific competition: ties were most common, and homosyndrome only occurred in poor competitors. In the context of rapid Arctic and west Antarctic warming and ice-loading of nearshore waters, we predict strongly changing patterns of intraspecific competition. Indeed we suggest that decreased patchiness of intra- versus interspecific competition and decreased levels of intraspecific competition should be strong indicators of increases in surface water ice-loading from ice-sheet collapses. KEYWORDS: Sublittoral · Benthos · Bioconstruction · Climate change · Homosyndrome
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We examined deep-sea epibenthic sledge isopod data from the Atlantic sector of the Southern Ocean (SO) (depth range=742–5,191 m). Samples were taken during the expeditions EASIZ II (ANT XV-3) in 1998 and ANDEEP I and II (ANT XIX3/4) in 2002. A total of 471 isopod species were recorded from 28 sites. The species richness of the epibenthic sledge samples was highly variable (6–82 species). Species richness was highest at site 131-3 in 3,053 m depth in the north-eastern Weddell Sea. The highest numbers of species were sampled in the middle depth range and lower species richness was found in the shallower and deeper parts of the study area. Depth is suggested to explain isopod species richness better than both latitude and longitude. Between 58°S and 65°S, the number of species ranged from 9 to 82 (mean=35.9). Further south in the Weddell Sea, between 73°S and 74°S, species richness was lower and the number of species ranged from 6 to 35 (mean=19.2). With regard to longitude, the highest species richness (up to 82 species) was found between 50°W and 60°W in the area of the South Shetland Islands and around the Antarctic Peninsula, while numbers did not exceed 50 species in the eastern Weddell Sea. The haul length, ranging from 807 to 6,464 m, was positively correlated with depth; however, there was no linear relationship between haul length and species richness. We therefore suggest that depth was the most important factor explaining isopod species richness. However, only 28 sites were visited and the statistical power is thus limited. Sampling in the deep sea is expensive and time consuming and as yet this is the best isopod data set available from the Atlantic sector of the SO. Future expeditions are therefore important to better explain the current patterns of benthic diversity in Antarctica.
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Inevitably, aerobic life leads to the formation of deleterious reactive oxygen species (ROS) which participate in biomolecule oxidation, hence augmenting biomolecule turnover. Organisms have adapted to counteract the noxious effects of ROS by developing a battery of antioxidant defences (AOX) which comprise enzymes and low-molecular weight scavengers. Past studies have reported elevated AOX levels in polar pectinid bivalves compared with temperate congeners. This fi nding is controversial as mitochondrial ROS generation is low in polar versus temperate species, and, to date, there is no generally accepted explanation of the causes of increased basal AOX levels in polar waters. We suggest that the low food availability in those ecosystems may result in polar marine ectotherms diverting some energy into the maintenance of high AOX. We tested this hypothesis by comparing the total oxyradical scavenging capacity (peroxyl, hydroxyl and peroxynitrite) of three clam species: Laternula elliptica (Antarctic), Mya truncata (Arctic) and Mya arenaria (temperate). The data confi rmed that polar bivalves are characterized by higher AOX. Herein, we propose that high AOX is required in environments characterized by low food availability as AOX effi ciently protects biomolecules, notably the RNA expressed at high levels by cold-water ectotherms. Also, high AOX may explain the relatively long lifespan of most polar ectotherms.
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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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Telonema is a widely distributed group of phagotrophic flagellates with two known members. In this study, the structural identity and molecular phylogeny of Telonema antarcticum was investigated and a valid description is proposed. Molecular phylogeny was studied using small-subunit rRNA (SSU rRNA) gene sequences. The pear-shaped cell had two subequal flagella that emerged laterally on the truncated antapical tail. One flagellum had tripartite hairs. The cell was naked, but had subsurface vesicles containing angular paracrystalline bodies of an unknown nature. A unique complex cytoskeletal structure, the subcortical lamina, was found to be an important functional and taxonomic feature of the genus. Telonema has an antero-ventral depression where food particles are ingested and then transferred to a conspicuous anterior food vacuole. The molecular phylogeny inferred from the SSU rRNA gene sequence suggested that Telonema represents an isolated and deep branch among the tubulocristate protists.
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A solitary skin lesion was found on the neck of a Weddell seal (Leptonychotes weddellii), chemically immobilized in Queen Maud Land (70°09′S, 05°22′E) Antarctica 2001. The lesion was elevated and 3cm in diameter, consisting of partly fresh and partly necrotic tissue, and proliferative papilloma-like structures were seen. Electron microscopy on a biopsy from the lesion revealed typical parapoxvirus particles. Polymerase chain reaction (PCR; B2L gene) generated amplicons of approximately 594 base pairs, comparable to Orf-virus, the prototype parapoxvirus. A comparison of these B2L PCR amplicon DNA sequences with corresponding sequences from other parapoxviruses, showed that the Weddell seal virus resembled isolates from grey seal (Halichoerus grypus) and harbour seal (Phoca vitulina) more than parapoxvirus from red deer (Cervus elaphus), sheep, cattle and Japanese serows (Capricornis crispus). It is thus concluded that the Weddell seal parapoxvirus belong to the tentative seal parapoxvirus species. Since parapox and orthopoxviruses may cause similar clinical diseases, we suggest that the term sealpox should be restricted to the clinical disease, whereas seal parapoxvirus should be used when caused by a parapoxvirus, rather than the general term “sealpox virus”. This is the first verified case of parapoxvirus infection in a Weddell seal, and also the first report of any such infections in the Antarctic.
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