|
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Tomasello, M. (1996). Do apes ape? In C. M. Heyes, & B. G. Galef (Eds.), Social learning in animals: the roots of culture (pp. 319–346). London: Academic Press.
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|
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Lefebvre, L., & Giraldeau, L. - A. (1996). Is social learning an adaptive specialisation? In C. M. Heyes, & B. G. Galef B. G..Jr. (Eds.), Social learning in animals: The root of culture (pp. 107–128). San Diego: Academic Press.
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Brückner, P. D. med. R. (1996). Dein Pferd, sein Auge, seine Sehweise. Basel: Selbstverlag.
Abstract: Inhalt u.a.: Das Pferdeauge, Sehorgan eines Weidegängers. Das Gesichtsfeld. Hornhaut und Pupille. Bewegungen des Augenpaares. Die Zusammenkoppelung der Augen. Sehschärfe. Scharfeinstellung des Auges für die Nähe. Stereopsis (“dreidimensionales” Sehen). Verhalten bei Blindheit mit verbundenen Augen. Augenkrankheiten bei Pferden. Überprüfung der Gesundheit des Pferdeauges.
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Packer, C., & Heinsohn, R. (1996). Response:Lioness leadership. Science, 271(5253), 1215–1216.
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Gary C. Jahn, & Craig Packer, R. H. (1996). Lioness leadership. Science, 271(5253), 1216–1219.
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de Waal, F. B. M., & Aureli, F. (1996). Consolation, reconciliation, and a possible cognitive difference between macaque and chimpanzee. In A. E. Russon, K. A. Bard, & S. T. Parker (Eds.), Reaching into Thought: The Minds of the Great Apes (pp. 80–110.). Cambridge: Cambridge University Press.
Abstract: Russon,A.E.; Bard, K.A.; Parker, S.T.
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King, S. R. B. (1996). The social behaviour of a bachelor group of Przewalski horses under free-ranging conditions. Queen Mary and Westfield College, .
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Zentall TR, Sutton JE, & Sherburne LM. (1996). True imitative learning in pigeons. Psychol. Sci., 7, 343.
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Zentall, T. R., Sutton, J. E., & Sherburne, L. M. (1996). True imitative learning in pigeons. Psychol Sci, 7.
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Barton, R. A. (1996). Neocortex size and behavioural ecology in primates. Proc. R. Soc. Lond. B, 263(1367), 173–177.
Abstract: The neocortex is widely held to have been the focus of mammalian brain evolution, but what selection pressures explain the observed diversity in its size and structure? Among primates, comparative studies suggest that neocortical evolution is related to the cognitive demands of sociality, and here I confirm that neocortex size and social group size are positively correlated once phylogenetic associations and overall brain size are taken into account. This association holds within haplorhine but not strepsirhine primates. In addition, the neocortex is larger in diurnal than in nocturnal primates, and among diurnal haplorhines its size is positively correlated with the degree of frugivory. These ecological correlates reflect the diverse sensory-cognitive functions of the neocortex.
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