Krinner G. & Werner M. (2003). Impact of precipitation seasonality changes on isotopic signals in polar ice cores : A multi-model analysis. Earth Planet. Sci. Lett., 216, 525–538.
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Bourgeon, S., Viera, V., Raclot, T. & Groscolas, R. (2007). Hormone and immunoglobulin levels in king penguins during molting and breeding fasts. Ecoscience, 14, 519–528.
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BOURGEON, S.; VIERA, V.M.; RACLOT, T.; GROSCOLAS, R. (2007). Hormones and immunoglobulin levels in king penguins during moulting and breeding fasts. Ecoscience, 14(4), 519–528.
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Benhamou S. (2006). Detecting an orientation component in animal paths when the preferred direction is individual-dependent. Ecology, 87(2), 518–528.
Abstract: An orientation component leads to directionally biased paths, with major consequences in animal population redistribution. Classical orientation analyses, which focus on the overall direction of motion, are useless for detecting such a component when the preferred direction is not common to the whole population, but differs from one path to another. In-depth path analyses are required in this case. They consist of determining whether paths are more suitably represented as biased or unbiased random walks. The answer is not easy because most animals' paths show some forward persistence propensity that acts as a purely local directional bias and, hence, blurs the possible occurrence of an additional, consistent bias in a preferred direction. I highlight the key differences between biased and unbiased random walks and the different ways orientation mechanisms can generate a consistent directional bias. I then examine the strength and weakness of the available methods likely to detect it. Finally, I introduce a new procedure based on the backward evolution of the beeline distance, from the end of the path, which might correspond to a goal toward which the animal orients itself, to each of the animal's preceding locations. This new procedure proves to be very efficient, as it requires only a small sample of short paths for detecting a possible orientation component
Programme: 421
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Pommereau J.P., Goutail F. & Sarkissian A. (1996). SAOZ total ozone measurements in antarctica; Comparisons with TOMS versions 6 and 7..
Abstract: proc. Third European Symp. on Polar Ozone
Programme: 209
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Criscuolo, F.; Bertile, F.; Durant, J. M.; Raclot, T.; Gabrielsen, G. W.; Massemin, S.; Chastel, O. (2006). Body Mass and Clutch Size May Modulate Prolactin and Corticosterone Levels in Eiders. Physiol. Biochem. Zool., 79(3), 514–521.
Abstract: Altered body condition, increased incubation costs, and egg loss are important proximate factors modulating bird parental behavior, since they inform the adult about its remaining chances of survival or about the expected current reproductive success. Hormonal changes should reflect internal or external stimuli, since corticosterone levels (inducing nest abandonment) are known to increase while body condition deteriorates, and prolactin levels (stimulating incubation) decrease following egg predation. However, in a capital incubator that based its investment on available body reserves and naturally lost about half of its body mass during incubation, corticosterone should be maintained at a low threshold to avoid protein mobilization for energy supply. This study focused on the regulation of corticosterone and prolactin release in such birds during incubation, when facing egg manipulation (control, reduced, or increased) or a stressful event. Blood samples were taken before and after clutch manipulation and at hatching. Corticosterone levels were determined before and after 30 min of captivity. Female eiders exhibited a high hypothalamic?pituitary?adrenal sensitivity, plasma concentration of corticosterone being increased by four? to fivefold following 30 min of captivity. The adrenocortical response was not modified by body mass loss but was higher in birds for which clutch size was increased. In the same way, females did not show different prolactin levels among the experimental groups. However, when incubation started, prolactin levels were correlated to body mass, suggesting that nest attendance is programmed in relation to the female initial body condition. Moreover, due to an artifactual impact of bird manipulation, increased baseline corticosterone was associated with a prolactin decrease in the control group. These data suggest that, in eiders, body mass and clutch size modification can modulate prolactin and corticosterone levels, which cross?regulate each other in order to finely control incubation behavior.
Programme: 332
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Masson-Delmotte V, Kageyama M, Braconnot P, Charbit S, Krinner G, Ritz C, Guilyardi E, Jouzel J, Abe-Ouchi A, Crucifix M, Gladstone RM, Hewitt CD, Kitoh A, LeGrande AN, Marti O, Merkel U, Motoi T, Ohgaito R, Otto-Bliesner B, Peltier WR, Ross I, Valdes PJ,. (2006). Past and future polar amplification of climate change: climate model intercomparisons and ice-core constraints. Climate dynamics, 26, 513–529.
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Jouventin, P. Couchoux, C. Dobson, F. S. (2009). UV signals in penguins. Polar Biol., 32, 513–514.
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Van Vliet Lanoë B., Vandenberghe N., Laignel B., Laurent M., Lauriat Rage A., Louwye S., Mansy J.L., Meilliez F., Mercier D Hallegouët B., Laquement F., Michel Y. & Moguedet G. (2002). Paleogeographic evolution of the Western Europe during the Upper Cenozoic. Geodiversitas, 24(3), 511–541.
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The Epica Dome C 2001 02 science and drilling teams. (2002). Extending the ice core record beyond half a million years. Eos, transactions, american geophysical union, 83(45), 509–517.
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