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Journal Abstract Search

317 related items for PubMed ID: 15961744

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  • 4. Energetic costs of diving and thermal status in European shags (Phalacrocorax aristotelis).
    Enstipp MR, Grémillet D, Lorentsen SH.
    J Exp Biol; 2005 Sep; 208(Pt 18):3451-61. PubMed ID: 16155218
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  • 5. Why do macaroni penguins choose shallow body angles that result in longer descent and ascent durations?
    Sato K, Charrassin JB, Bost CA, Naito Y.
    J Exp Biol; 2004 Nov; 207(Pt 23):4057-65. PubMed ID: 15498951
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  • 6. Air sac PO2 and oxygen depletion during dives of emperor penguins.
    Knower Stockard T, Heil J, Meir JU, Sato K, Ponganis KV, Ponganis PJ.
    J Exp Biol; 2005 Aug; 208(Pt 15):2973-80. PubMed ID: 16043602
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  • 9. Aerobic dive limit. What is it and is it always used appropriately?
    Butler PJ.
    Comp Biochem Physiol A Mol Integr Physiol; 2006 Sep; 145(1):1-6. PubMed ID: 16846744
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  • 14. Dive behaviour impacts the ability of heart rate to predict oxygen consumption in Steller sea lions (Eumetopias jubatus) foraging at depth.
    Young BL, Rosen DA, Hindle AG, Haulena M, Trites AW.
    J Exp Biol; 2011 Jul 01; 214(Pt 13):2267-75. PubMed ID: 21653820
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  • 17. Energetic cost of foraging in free-diving emperor penguins.
    Nagy KA, Kooyman GL, Ponganis PJ.
    Physiol Biochem Zool; 2001 Jul 01; 74(4):541-7. PubMed ID: 11436138
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  • 18. To what extent is the foraging behaviour of aquatic birds constrained by their physiology?
    Green JA, Halsey LG, Butler PJ.
    Physiol Biochem Zool; 2005 Jul 01; 78(5):766-81. PubMed ID: 16075394
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  • 19. Metabolic regulation in diving birds and mammals.
    Butler PJ.
    Respir Physiol Neurobiol; 2004 Aug 12; 141(3):297-315. PubMed ID: 15288601
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