|
Hureau J.C. (1993). Un antigel dans le sang des poissons. (Vol. 170).
|
|
|
Weimerskirch, H., Pinaud, D, Pawlowski, F. & Bost, CA. (2007). Does Prey Capture Induce Area-Restricted Search? A Fine-Scale Study Using GPS in a Marine Predator,the Wandering Albatross capture and GPS. Am. Nat., 170(5), 735–743.
|
|
|
Jouanne, F., T. Villemin, A. Berger, and O. Henriot. (2006). Rift-transform Junction in North-Iceland: rigid blocks and narrow accommodation zones revealed by GPS 1997-1999-2002. Geophysical journal international, 167, 1439–1447.
|
|
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Nicolas, J., J.-M. Nocquet, M. Van Camp, T. van Dam, J.-P. Boy, J. Hinderer, P. Gegout, E. Calais, M. Amalvict. (2006). Seasonal effect on vertical positioning by Satellite Laser Ranging and Global Positioning System and on absolute gravity at the OCA geodetic station, Grasse, France. Geophysical journal international, 167, 1127–1137.
|
|
|
Giret A. (1994). Hommage, l'oeuvre de Jean Lameyre aux Kerguelen. Memoires de la societe geologique de france, 166.
|
|
|
Bonin B., Bardintzeff J.M., & Giret A. (1994). The distribution of felsic rocks within the alkaline igneous centres. Memoires de la societe geologique de france, 166.
|
|
|
Maggi A., Debayle E., Priestley K. & Barruol G. (2006). Multi-mode surface waveform tomography of the Pacific Ocean: A closer look at lithospheric cooling. Geophysical journal international, 166, 1384–1397.
|
|
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Sato, T., Okuno, J., Hinderer, J., MacMillan, D. S., Plag, H.-P., Francis, O., Falk, R. and Fukuda, Y. (2006). A geophysical interpretation of the secular displacement and gravity rates observed at Ny-Alesund, Svalbard in the Arctic- Effects of the post-glacial rebound and present-day ice melting. Geophysical journal international, 165, 729–743.
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Angelier F., Chastel O. (2009). Stress, prolactin and parental investment in birds: a review. Gen. Comp. Endocrinol., 163, 142–148.
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ANGELIER F, CHASTEL O. (2009). Stress, prolactin and parental investment in birds: A review. Gen. Comp. Endocrinol., 163, 142–148.
Abstract: In this paper, we review the relationships that link avian parental behavior, stress (acute or chronic) and energetic constraints to the secretion of prolactin, the ‘parental hormone’. Prolactin secretion is stimulated by exposure of the parent to tactile and visual stimuli from the nest, the eggs or the chicks, while prolactin facilitates/stimulates the expression of parental behaviors, such as incubating, brooding or feeding. Because of this role of prolactin in the expression of parental behaviors, we suggest that absolute circulating prolactin levels may reflect to the extent to which individuals provide parental care (i.e., parental effort). Stressors and energetic constraints (acute or chronic) depress prolactin levels (‘the prolactin stress response’) and this may be adaptive because it may disrupt the current parental effort of an individual and promote its survival. Alternatively, an attenuation of the prolactin stress response can be considered as a hormonal tactic permitting the maintenance of parental care to the detriment of parental survival during stressful situations. Therefore, we suggest that the magnitude of the prolactin stress response may reflect parental investment. Finally, we detail the interaction that links corticosterone, prolactin and stress in bird parents. We suggest that corticosterone and prolactin may mediate different components of the stress response, and, therefore, we emphasize the importance of considering both hormones when investigating the hormonal basis of parental investment.
Programme: 330
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