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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An infiltration community was the dominating ice algal community in pack-ice off Queen Maud Land, Southern Ocean, in January 1993. The community was dominated by autotrophic processes, and the most common species were the prymnesiophyte Phaeocystis antarctica and the diatoms Chaetoceros neglectus and Fragilariopsis cylindrus. The concentration of chlorophyll a was 1.3–47.9 μg l−1, and the inner part of the community was nitrate depleted. Uptake rates of nitrate, nitrite, ammonium, urea and amino acids were measured using 15N. Nitrate was the major nitrogen source for ice algal growth (67 ± 6% nitrate uptake). It is suggested that % nitrate uptake in the infiltration community decreases during the growth season, from 92% during spring (literature data) to 67% during summer. Scalar irradiance in the infiltration community was high and variable. It reached ca. 2000 μmol m−2 s−1 at some locations, and nitrate uptake rate was potentially photoinhibited at irradiances >500 μmol m−2 s−1. Nitrate uptake rate in an average infiltration community (0.6 m of snow cover) was lowered by 13% over a 2-week period due to photoinhibition.
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The efficiency of physical concentration mechanisms for enrichment of algae and bacteria in newly formed sea-ice was investigated under defined conditions in the laboratory. Sea-ice formation was simulated in a 3,000 l tank under different patterns of water movement. When ice formed in an artificially generated current pattern, algal cells were substantially enriched within the ice matrix. Enrichment factors for chlorophyll a calculated from the ratio between the concentrations in ice and underlying water reached values of up to 53. Repeated mixing of ice crystals into the water column, as well as flow of water through the new ice layer, contributed to the enrichment of algae in the ice. Wave action during ice formation revealed lower phytoplankton enrichment factors of up to 9. Mixing of floating ice crystals with underlying water and pumping of water into the ice matrix by periodical expansion and compression of the slush ice layer were responsible for the wave-induced enrichment of algal cells. Physical enrichment of bacteria within the ice was negligible. Bacterial biomass within new ice was enhanced only when the concentration of algae was high. At low algal biomass, bacteria experienced substantial losses in the ice, most likely due to brine drainage, which were not observed for the microalgae. Bacterial cells are therefore not scavenged by ice crystals and the observed enrichment and sustainment of bacterial biomass within newly formed ice depend on their attachment to cells or aggregates of algae. Division rates of bacteria changed only slightly during ice formation.
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Microscopical examination of near-surface eucaryotic microbial populations in circumcontinental waters of Antarctica indicated that nanoplankton (<20 μm diameter) dominated in regions with low chlorophyll concentrations (< 1 μg l⁻¹). About 30 % of the mean nanoplankton carbon consisted of heterotrophic flagellates. Heterotrophic microplankton carbon (> 20 μm diameter) was generally less significant. The variation in phytoplankton biomass was the result primarily of changes in cell density of pennate diatoms in the East Wind Drift, and of centric diatoms in the Weddell Sea and the Scotia Ridge region. Autotrophic and heterotrophic carbon as determined by microscopical analysis were compared with data for total particulate carbon, chlorophyll a, and adenosine triphosphate. Estimates for the C:chl ratio of autotrophs increased with decreasing concentrations of chlorophyll a, with mean values of 46 in bloom waters and 144 in 'blue water'. A C:ATP ratio for heterotrophic nanoplankton was estimated to be about 100, while that for heterotrophic microplankton may be lower. Algorithms, incorporating concentrations of chlorophyll a and ATP, are described which allow estimates of autotrophic and heterotrophic microbial biomass.
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Some Nitzschia and closely related species have been examined in the light and electron microscopes from fast ice samples in the Arctic and Antarctic. Nitzschia neofrigida, forming arborescent colonies, and Nitzschia promare, forming loose ribbon colonies, are described as new species, both probably included in the distribution of other similar species. A new combination, Auricula compacta, represents the first report of this genus from ice samples. Colony formation is reported for the first time in Nitzschia arctica and Nitzschia taeniiformis. No biopolar species were found and several reports of Arctic species in Antarctic ice samples have been refuted.
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The response of phytoplankton to variations in the light regime was studied during the VULCAN and ACDA cruises in the Antarctic. Unenriched batch cultures of 12–19 days' duration reached chl concentrations of 10–50 μg−1 and exhibited exponential growth rates, with the maximal rate being 0.41 doubl, day−1. Ice edge algae exhibited maximum growth rates at photon flux densities (PFD) of 30–100 μE m−2S−1 and the growth rate was reduced by about 30% at 500–1000 μE m−2S−1 The chl/C ratio ranged between 0.004 and 0.018, with the lowest ratios at PFDs above 500 μE m−2S−1 chl/C ratios were also below maximum at PFDs below 40–50 μE m−2S−1 The C:N:P ratios were close to the Redfield ratios; the Si/C ratio averaged 0.16 (atoms), and the ATP/C ratio averaged from 0.0024 to 0.0050 in different culture senes. When thawed after having been frozen for 10 days, shade-adapted cultures were in a much better condition than sun-adapted ones. P versus I data showed that the maximum assimilation number varied from 0.75 to 4.4 μg C (μg chl)−1h−1. It varied inversely with the chl/C ratio; therefore the maximum carbon turnover rate varied little between samples (0.024/0.035 h−1). Low biomass communities exhibited relatively high values for α (the initial slope of P versus I curves), low values for 1sat (160–330 μE m−2S−1), and they were susceptible to photoinhibition. In contrast, communities dominated by Odontella weissflogii exhibited low values for α, a high value for Isat (560 μE m−2S−1 and they tolerated high PFDs. The photo-adaptational status of the phytoplankton in natural water samples is discussed relative to the profile of water column stability and mixing processes.
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- alger
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