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 28 resources

  • We report on ground-based atmospheric measurements and emission estimates of the four anthropogenic hydrofluorocarbons (HFCs) HFC-365mfc (CH3CF2CH2CF3, 1,1,1,3,3-pentafluorobutane), HFC-245fa (CHF2CH2CF3, 1,1,1,3,3-pentafluoropropane), HFC-227ea (CF3CHFCF3, 1,1,1,2,3,3,3-heptafluoropropane), and HFC-236fa (CF3CH2CF3, 1,1,1,3,3,3-hexafluoropropane). In situ measurements are from the global monitoring sites of the Advanced Global Atmospheric Gases Experiment (AGAGE), the System for Observations of Halogenated Greenhouse Gases in Europe (SOGE), and Gosan (South Korea). We include the first halocarbon flask sample measurements from the Antarctic research stations King Sejong and Troll. We also present measurements of archived air samples from both hemispheres back to the 1970s. We use a two-dimensional atmospheric transport model to simulate global atmospheric abundances and to estimate global emissions. HFC-365mfc and HFC-245fa first appeared in the atmosphere only ∼1 decade ago; they have grown rapidly to globally averaged dry air mole fractions of 0.53 ppt (in parts per trillion, 10−12) and 1.1 ppt, respectively, by the end of 2010. In contrast, HFC-227ea first appeared in the global atmosphere in the 1980s and has since grown to ∼0.58 ppt. We report the first measurements of HFC-236fa in the atmosphere. This long-lived compound was present in the atmosphere at only 0.074 ppt in 2010. All four substances exhibit yearly growth rates of >8% yr−1 at the end of 2010. We find rapidly increasing emissions for the foam-blowing compounds HFC-365mfc and HFC-245fa starting in ∼2002. After peaking in 2006 (HFC-365mfc: 3.2 kt yr−1, HFC-245fa: 6.5 kt yr−1), emissions began to decline. Our results for these two compounds suggest that recent estimates from long-term projections (to the late 21st century) have strongly overestimated emissions for the early years of the projections (∼2005–2010). Global HFC-227ea and HFC-236fa emissions have grown to average values of 2.4 kt yr−1 and 0.18 kt yr−1 over the 2008–2010 period, respectively.

  • The oceans play a key role in climate regulation especially in part buffering (neutralising) the effects of increasing levels of greenhouse gases in the atmosphere and rising global temperatures. This chapter examines how the regulatory processes performed by the oceans alter as a response to climate change and assesses the extent to which positive feedbacks from the ocean may exacerbate climate change. There is clear evidence for rapid change in the oceans. As the main heat store for the world there has been an accelerating change in sea temperatures over the last few decades, which has contributed to rising sea‐level. The oceans are also the main store of carbon dioxide (CO2), and are estimated to have taken up ∼40% of anthropogenic-sourced CO2 from the atmosphere since the beginning of the industrial revolution. A proportion of the carbon uptake is exported via the four ocean ‘carbon pumps’ (Solubility, Biological, Continental Shelf and Carbonate Counter) to the deep ocean reservoir. Increases in sea temperature and changing planktonic systems and ocean currents may lead to a reduction in the uptake of CO2 by the ocean; some evidence suggests a suppression of parts of the marine carbon sink is already underway. While the oceans have buffered climate change through the uptake of CO2 produced by fossil fuel burning this has already had an impact on ocean chemistry through ocean acidification and will continue to do so. Feedbacks to climate change from acidification may result from expected impacts on marine organisms (especially corals and calcareous plankton), ecosystems and biogeochemical cycles. The polar regions of the world are showing the most rapid responses to climate change. As a result of a strong ice–ocean influence, small changes in temperature, salinity and ice cover may trigger large and sudden changes in regional climate with potential downstream feedbacks to the climate of the rest of the world. A warming Arctic Ocean may lead to further releases of the potent greenhouse gas methane from hydrates and permafrost. The Southern Ocean plays a critical role in driving, modifying and regulating global climate change via the carbon cycle and through its impact on adjacent Antarctica. The Antarctic Peninsula has shown some of the most rapid rises in atmospheric and oceanic temperature in the world, with an associated retreat of the majority of glaciers. Parts of the West Antarctic ice sheet are deflating rapidly, very likely due to a change in the flux of oceanic heat to the undersides of the floating ice shelves. The final section on modelling feedbacks from the ocean to climate change identifies limitations and priorities for model development and associated observations. Considering the importance of the oceans to climate change and our limited understanding of climate-related ocean processes, our ability to measure the changes that are taking place are conspicuously inadequate. The chapter highlights the need for a comprehensive, adequately funded and globally extensive ocean observing system to be implemented and sustained as a high priority. Unless feedbacks from the oceans to climate change are adequately included in climate change models, it is possible that the mitigation actions needed to stabilise CO2 and limit temperature rise over the next century will be underestimated.

  • A new climate simulation for the middle Pliocene (ca. 3 Ma BP) is performed by a global grid-point atmospheric general circulation model developed at the Institute of Atmospheric Physics (IAP AGCM) with boundary conditions provided by the U. S. Geological Survey's Pliocene Research, Interpretations, and Synoptic Mapping (PRISM) group. It follows that warmer and slightly wetter conditions dominated at the middle Pliocene with a globally annual mean surface temperature increase of 2.60°C, and an increase in precipitation of 4.0% relative to today. At the middle Pliocene, globally annual terrestrial warming was 1.86°C, with stronger warming toward high latitudes. Annual precipitation enhanced notably at high latitudes, with the augment reaching 33.5% (32.5%) of the present value at 60–90°N (60–90°S). On the contrary, drier conditions were registered over most parts at 0–30°N, especially in much of East Asia and the northern tropical Pacific. In addition, both boreal summer and winter monsoon significantly decreased in East Asia at the middle Pliocene. It is indicated that the IAP AGCM simulation is generally consistent with the results from other atmospheric models and agrees well with available paleoclimatic reconstructions in East Asia. Additionally, it is further revealed that the PRISM warmer sea surface temperature and reduced sea ice extent are main factors determining the middle Pliocene climate. The simulated climatic responses arising from the PRISM reconstructed vegetation and continental ice sheet cannot be neglected on a regional scale at mid to high latitudes (like over Greenland and the Qinghai-Tibetan Plateau, and around the circum-Antarctic) but have little influence on global climate.

  • The most consistent means of investigating the global sea ice cover is by satellite passive microwave sensors, as these are independent of illumination and cloud cover. The Nimbus 7 Scanning Multichannel Microwave Radiometer (SMMR) and the Defense Meteorological Satellite Program (DMSP) Special Sensor Microwave Imager (SSMI) provide information on the global sea ice cover from 1978 to present. The two instruments flew simultaneously during a 6-week overlap period in July and August 1987, thus enabling intercomparison of the two sensors. Brightness temperatures are corrected for instrument drift and calibration differences in order to produce continuous time series of monthly averaged Arctic and Antarctic sea ice extent and sea ice area through the use of the NOrwegian Remote Sensing EXperiment (NORSEX) algorithm, which relates brightness temperatures to ice concentration. Statistical analysis on the time series estimates the decreases in Arctic ice extent and ice area to be 4.5% and 5.7%, respectively, during the 16.8-year observation period. The overall trends established here serve to better define and strengthen earlier assertions of a reduced ice cover, based on analysis of SMMR and SSMI data taken separately. These results are consistent with GCM simulations that suggest retreat of the sea ice cover under global warming scenarios.

  • Until 1985 most studies of CO2 in gas inclusions in pre-industrial ice indicated that CO2 concentrations (up to 2450 ppm) were higher than the current atmospheric level. After 1985, lower pre-industrial CO2 values were reported, and used as evidence for a recent man-made CO2 increase. The errors in these revised values, however, are of a similar magnitude to the apparent increase in atmospheric CO2 level. The assumptions used in estimating lower CO2 values in past atmospheres have been: no liquid phase in polar ice; younger age of air than of ice due to free gas exchange between deep firn and the atmosphere; and no change in composition of air inclusions. These assumptions are shown to be invalid. Liquid saline water exists in ice at low temperatures, even below −70°C; airtight ice layers are ubiquitous in Antarctic firn; and more than 20 physico-chemical processes operating in situ and in ice cores contribute to the alteration of the chemical composition of air inclusions. The permeable ice sheet with its capillary liquid network acts as a sieve which redistributes elements, isotopes, and micro-particles. Thirty-six to 100% of air recovered from old ice is contaminated by recent atmospheric air during field and laboratory operations. The value of ∼290 ppm, widely accepted from glacier studies for the pre-industrial atmospheric CO2 level, apparently results from: invalid assumptions; processes in ice sheets; artifacts in ice cores; and arbitrary rejection of high readings. To date, glaciological studies are not able to provide a reliable reconstruction of either the CO2 level in pre-industrial and ancient atmospheres or paleoclimates. Instead these studies have led to a widely accepted false dogma of man-made climatic warming. This dogma may have enormous negative impact on our common future.

Last update from database: 3/1/25, 3:17 AM (UTC)

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