Search

To improve our understanding of wintertime polar ozone losses, two ozonesonde Match campaigns were performed. The first one was carried out in the Arctic winter 2002/03. About 450 coordinated ozonesondes were launched from late November 2002 to March 2003. Temperatures low enough for the formation of polar stratospheric clouds (PSC) occurred already in the second half of November. At 475 K the Match analysis shows increasing ozone loss rates from early December until the second half of January with peaking loss rates of 35 ppbv/day. Afterwards the rate of ozone loss decreased and stopped after a month. Throughout the whole winter we find accumulated ozone loss of about 1.5 ppmv at the 500 K isentrope and approximately 60 DU in the total ozone column, which is about half of the maximum loss found in past winters. From June to October 2003 an Antarctic Match campaign was carried out for the first time. About 400 sondes were launched by 9 stations. Ozone loss rates of up to 75 ppbv/day were found inside the polar vortex at the 475 K potential temperature level during the first half of September. The timing of the fastest ozone loss coincides with the return of sunlight to the vortex after the Antarctic winter. During the whole time period temperatures were low enough for PSCs, including ice clouds, to form. Results for the potential temperature range between 400 K and 550 K will be presented.

The role of iron and light in controlling photosynthate production and allocation in phytoplankton populations of the Atlantic sector of the Southern Ocean was investigated in April–May 1999. The 14C incorporation into five biochemical pools (glucan, amino acids, proteins, lipids and polysaccharides) was measured during iron/light perturbation experiments. The diurnal Chl a-specific rates of carbon incorporation into these pools did not change in response to iron addition, yet were decreased at 20 μmol photons m−2 s−1, an irradiance comparable with the one at 20–45 m in situ depth. This suggests that the low phytoplankton biomass encountered (0.1–0.6 μg Chl a L−1) was mainly caused by light limitation in the deep wind mixed layer (>40 m). Regional differences in Chl a-specific carbon incorporation rates were not found in spite of differences in phytoplankton species composition: at the Antarctic Polar Front, biomass was dominated by a diatom population of Fragilariopsis kerguelensis, whereas smaller cells, including chrysophytes, were relatively more abundant in the Antarctic Circumpolar Current beyond the influence of frontal systems. Because mixing was often in excess of 100 m in the latter region, diatom cells may have been unable to fulfil their characteristically high Fe demand at low average light conditions, and thus became co-limited by both resources. Using a model that describes the 14C incorporation, the consistency was shown between the dynamics in the glucan pool in the field experiments and in laboratory experiments with an Antarctic diatom, Chaetoceros brevis. The glucan respiration rate was almost twice as high during the dark phase as during the light phase, which is consistent with the role of glucan as a reserve supplying energy and carbon skeletons for continued protein synthesis during the night.

Life histories are state-dependent, and an individual's reproductive decisions are determined by its available resources and the needs of its offspring. Here we test how a chick's needs for food and protection influence parental decisions in the Antarctic petrel, Thalassoica antarctica, where the parents, due to their long breeding lifespan, are expected to give priority to their own needs before those of the young. We exchanged one-day-old chicks with four-day-old chicks and studied how the parents subsequently provided care to the chick. The duration of the guarding period was adjusted, and parents left older chicks earlier and younger chicks later compared to controls. Three mechanisms were responsible for the adjustments. 1) Parents with an older chick co-ordinated fewer guarding spells whereas parents with a younger chick co-ordinated more guarding spells. 2) At the last guarding spell, i.e. where a parent left the chick alone before the partner returned, less time was spent with older chicks, and more time with younger chicks. 3) Foraging trip duration was shortened by parents given older chicks and prolonged by parents given younger chicks, probably in response to the chick's food demand. Hence, the parents responded quickly to the altered needs of the chick. Parents with high body mass guarded longer and were better able to co-ordinate the guarding spells compared to lighter parents. In conclusion, Antarctic petrels adjust reproductive decisions to their own, their mate's, and their chick's state, and they seem to respond to the chick's needs for both food and protection.

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.

Ocean Drilling Program Site 1165 penetrated drift sediments on the East Antarctic continental rise and recovered sediments from a low-energy depositional environment. The sediments are characterized by prominent alternations between a green to greenish-gray diatom-bearing hemipelagic facies and gray to dark gray hemiturbiditic facies. Our investigation of an upper Miocene section, using high-resolution color spectra, multisensor core logs, and X-ray fluorescence scans, reveals that sedimentation changes occur at Milankovitch orbital frequencies of obliquity and precession. We use this finding to derive an astronomical calibrated time scale and to calculate iron mass-accumulation rates, as a proxy for sediment-accumulation rates. Terrigenous iron fluxes change by as much as 100% during each obliquity cycle. This change and an episodic pattern of enhanced ice-rafted debris deposition during times of deglaciation provide evidence for a dynamic and likely wet-based late Miocene East Antarctic Ice Sheet (EAIS) that underwent large size variations at orbital time scales. The dynamic behavior of the EAIS implies that a significant proportion of the variability seen in oxygen isotope records of the late Miocene reflects Antarctic ice-volume changes.

In previous work, whaling catch positions were used as a proxy record for the position of the Antarctic sea ice edge and mean sea ice extent greater than the present one spanning 2.8° latitude was postulated to have occurred in the pre-1950s period, compared to extents observed since 1973 from microwave satellite imagery. The previous conclusion of an extended northern latitude for ice extent in the earlier epoch applied only to the January (mid-summer) period. For this summer period, however, there are also possible differences between ship and satellite-derived measurements. Our work showed a consistent summer offset (November– December), with the ship-observed ice edge 1 - 1.5° north of the satellitederived ice edge. We further reexamine the use of whale catch as an ice edge proxy where agreement was claimed between the satellite ice edge (1973–1987) and the ship whale catch positions. This examination shows that, while there may be a linear correlation between ice edge position and whale catch data, the slope of the line deviates from unity and the ice edge is also further north in the whale catch data than in the satellite data for most latitudes. We compare the historical (direct) record and modern satellite maps of ice edge position accounting for these differences in ship and satellite observations. This comparison shows that only regional perturbations took place earlier, without significant deviations in the mean ice extents, from the pre-1950s to the post-1970s. This conclusion contradicts that previously stated from the analysis of whale catch data that indicated Antarctic sea ice extent changes were circumpolar rather than regional in nature between the two periods.

Dronning Maud Land contains a fragment of an Archaean craton covered by sedimentary and magmatic rocks of Mesoproterozoic age, surrounded by a Late Mesoproterozoic metamorphic belt. Tectonothermal events at the end of the Mesoproterozoic and in Late Neoproterozoic–Cambrian times (Pan-African) have been proved within the metamorphic belt. In western Dronning Maud Land a juvenile Mesoproterozoic basement was accreted to the craton at c. 1.1 Ga. Mesoproterozoic rocks were also detected by zircon SHRIMP dating of gneisses in central Dronning Maud Land, followed by a long hiatus for which geochronological data are lacking, an amphibolite to granulite facies metamorphism and syntectonic granitoid emplacement of Pan-African age have been dated. During this orogeny older structures were completely overprinted in a sinistral tranpressive deformation regime, leading to the mainly coast-parallel tectonic structures of the East Antarctic Orogen. Putting Antarctica back in its Gondwana position, the East Antarctic Orogen continues northward in East Africa as the East African Orogen, whereas a connection to the marginal Ross Orogen at the Pacific margin of East Antarctica is suggested along the Shackleton Range. The East Antarctic-East African Orogen resulted from closure of the Mozambique Ocean and collision of West and East Gondwana, i.e. western Dronning Maud Land was part of West Gondwana. During this collision the lithospheric mantle probably delaminated, allowing the asthenosphere to underplate the continental crust and producing heat for the voluminous, typically anhydrous, Pan-African granitoids of central Dronning Maud Land.

A new stegocephalid (Amphipoda) species, Metandania tordi n.sp, is described, belonging to the subfamily Andaniexinae Berge & Vader 2001. The new species is the first record of the genus in the southern hemisphere. In addition, a morphological trait, previously not figured nor described within this family, is presented: a process proximally on the inner anterior surface of the fourth coxa. This locking-process is interpreted, and named accordingly, to enhance a relative stabilization of the third and fourth coxae. A brief comparison of the morphology of the fourth coxa between all five stegocephalid subfamilies is presented.

A large database of rocket measurements of the D-region electron concentration has been studied. The data were obtained at four sites in the Antarctic (Molodezhnaya and Syowa) and Arctic (Heiss Island, and Andøya/Kiruna). The electron densities were analysed in terms of their variations with solar zenith angle, geomagnetic activity and atmospheric temperature. We found that there is a particle ionisation source in the auroral oval even in quiet conditions. The energy of the particles is such, that they penetrate down to 85km, are partially absorbed between 85 and 80km but do not penetrate (are completely absorbed) below 75km. Analysis of the dependence of the electron concentration [e] on the daily sum of Kp indices, ∑Kp, shows that at all heights considered there is an increase of [e] with ∑Kp up to some saturation value of ∑Kp and beyond this level [e] is either constant (with large scatter of the data) or even decreases. This indicates that when the auroral oval expands with increasing geomagnetic activity, a particular station may move from a position outside or at the boundary of the oval, to a position inside the polar cap. An attempt is made to find the temperature dependence of the electron concentration. It is found that [e] at 75 and 80km increases with temperature T. Analysis of the flights conducted during noctilucent cloud (NLC) events at Andøya/Kiruna reveals a strong dependence of [e] on ∑Kp at 80 and 85km. This dependence is stronger and better defined than that for the entire data set. This may be explained by the low mesopause temperatures observed in summer when NLC occur. A comparison of the electron density data sets with empirical and theoretical models is presented and during quiet magnetic conditions a good agreement with mid-latitude models is found.

Sea ice is a remarkable component of the global climate system. It can form over up to about 10 % of the global ocean area, and creates an insulating barrier between the relatively warm seawater and the cold atmosphere, allowing a temperature difference that may be tens of degrees over only a couple of meters. It reduces evaporation from the ocean, leading to a drier atmosphere than would otherwise exist. Sea ice modifies the radiation balance at the Earth’s surface because it supports snow (the most reflective of the Earth’s natural surfaces, with an albedo of up to approximately 0.8), where otherwise there would be seawater (the least reflective, with an albedo of about 0.07). As sea ice forms it excludes brine, deepening the ocean surface mixed layer and influencing the formation of deep and bottom water. As it melts, it releases relatively fresh water, stratifying the upper layers of the ocean. Through these processes sea ice exerts an enormous influence on the atmospheric and oceanic circulation in cold regions and indeed the climate of the rest of the globe.

How animals change their movement patterns in relation to the environment is a central topic in a wide area of ecology, including foraging ecology, habitat selection, and spatial population ecology. To understand the underlying behavioral mechanisms involved, there is a need for methods to measure changes in movement patterns along a pathway through the landscape. We used simulated pathways and satellite tracking of a long-ranging seabird to explore the properties of first-passage time as a measure of search effort along a path. The first-passage time is defined as the time required for an animal to cross a circle with a given radius. It is a measure of how much time an animal uses within a given area. First-passage time is scale dependent, and a plot of variance in first-passage time vs. spatial scale reveals the spatial scale at which the animal concentrates its search effort. By averaging the first-passage time on a geographical grid, it is possible to relate first-passage time to environmental variables and the search pattern of other individuals.

A hindcast simulation of the Arctic and Antarctic sea ice variability during 1955–2001 has been performed with a global, coarse resolution ice–ocean model driven by the National Centers for Environmental Prediction / National Center for Atmospheric Research reanalysis daily surface air temperatures and winds. Both the mean state and variability of the ice packs over the satellite observing period are reasonably well reproduced by the model. Over the 47-year period, the simulated ice area (defined as the total ice-covered oceanic area) in each hemisphere experiences large decadal variability together with a decreasing trend of ~1 % per decade. In the Southern Hemisphere, this trend is mostly caused by an abrupt retreat of the ice cover during the second half of the 1970s and the beginning of the 1980s. The modelled ice volume also exhibits pronounced decadal variability, especially in the Northern Hemisphere. Besides these fluctuations, we detected a downward trend in Arctic ice volume of 1.8 % per decade and an upward trend in Antarctic ice volume of 1.5 % per decade. However, caution must be exercised when interpreting these trends because of the shortness of the simulation and the strong decadal variations. Furthermore, sensitivity experiments have revealed that the trend in Antarctic ice volume is model-dependent.

A 12.5 m long core was retrieved from the continental margin off Dronning Maud Land, Antarctica. Magnetostratigraphy, stable isotopes, 14C accelerator mass spectrometer and amino acid analyses indicate a continuous sediment record going back 1.3 Myr. Comparison of CaCO3 results with those from ODP Site 1089 and an index of North Atlantic Deep Water (NADW) influence in surface waters indicate that NADW upwelled along the Antarctic continental margin during the whole of this period. The mid-Pleistocene transition (1.0–0.6 Ma) was accompanied by an apparent decline in the NADW influence, and was followed by extended carbonate dissolution during the interglacials of marine isotope stages (MIS) 13 and 11. Less extensive periods of dissolution occur at the end of the interglacials younger than MIS 11. While interglacial dissolution is characteristic of the Pacific and Indian oceans, the carbon isotopes return to pre-transition values indicative of renewed NADW upwelling. The concentration of ice-rafted debris may reflect changes in the relative rate of interglacial sedimentation. It is speculated that the high ice rafted debris (IRD) concentrations during interglacials younger than 400 kyr may be due to a reduced relative sedimentation rate of other interglacial components whereas the low concentrations during interglacials before the mid-Pleistocene transition may be due to a higher relative sedimentation rate of these.

A new coupled atmosphere–ocean–sea ice model has been developed, named the Bergen Climate Model (BCM). It consists of the atmospheric model ARPEGE/IFS, together with a global version of the ocean model MICOM including a dynamic–thermodynamic sea ice model. The coupling between the two models uses the OASIS software package. The new model concept is described, and results from a 300-year control integration is evaluated against observational data. In BCM, both the atmosphere and the ocean components use grids which can be irregular and have non-matching coastlines. Much effort has been put into the development of optimal interpolation schemes between the models, in particular the non-trivial problem of flux conservation in the coastal areas. A flux adjustment technique has been applied to the heat and fresh-water fluxes. There is, however, a weak drift in global mean sea-surface temperature (SST) and sea-surface salinity (SSS) of respectively 0.1 °C and 0.02 psu per century. The model gives a realistic simulation of the radiation balance at the top-of-the-atmosphere, and the net surface fluxes of longwave, shortwave, and turbulent heat fluxes are within observed values. Both global and total zonal means of cloud cover and precipitation are fairly close to observations, and errors are mainly related to the strength and positioning of the Hadley cell. The mean sea-level pressure (SLP) is well simulated, and both the mean state and the interannual standard deviation show realistic features. The SST field is several degrees too cold in the equatorial upwelling area in the Pacific, and about 1 °C too warm along the eastern margins of the oceans, and in the polar regions. The deviation from Levitus salinity is typically 0.1 psu – 0.4 psu, with a tendency for positive anomalies in the Northern Hemisphere, and negative in the Southern Hemisphere. The sea-ice distribution is realistic, but with too thin ice in the Arctic Ocean and too small ice coverage in the Southern Ocean. These model deficiencies have a strong influence on the surface air temperatures in these regions. Horizontal oceanic mass transports are in the lower range of those observed. The strength of the meridional overturning in the Atlantic is 18 Sv. An analysis of the large-scale variability in the model climate reveals realistic El Niño – Southern Oscillation (ENSO) and North Atlantic–Arctic Oscillation (NAO/AO) characteristics in the SLP and surface temperatures, including spatial patterns, frequencies, and strength. While the NAO/AO spectrum is white in SLP and red in temperature, the ENSO spectrum shows an energy maximum near 3 years.