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1

N, Hughes R., ed. Diet selection: An interdisciplinary approach to foraging behaviour. Oxford: Blackwell Scientific Publications, 1993.

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2

Redhead, Edward. Foraging behaviour in rats: Experimental investigation in the laboratory. Birmingham: University of Birmingham, 1989.

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3

Burness, Gary P. Foraging ecology and parental behaviour in the common tern (Sterna hirundo). St. Catharines, [Ont.]: Dept. of Biological Sciences, Brock University, 1992.

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4

Saint-Jacques, Nathalie. Flexibility, and the foraging behaviour of the white sucker (catostomus commersoni). Ottawa: National Library of Canada, 1996.

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5

Kamil, Alan C., John R. Krebs, and H. Ronald Pulliam, eds. Foraging Behavior. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1839-2.

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6

Wageningen, Landbouwuniversiteit, ed. Foraging behaviour of the egg parasitoid Uscana lariophaga towards biological control of bruchid pests in stored cowpea in West Africa. Wageningen: [s.n], 1996.

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7

1955-, Stephens David W., Brown Joel S. 1959-, and Ydenberg Ronald C, eds. Foraging: Behavior and ecology. Chicago: University of Chicago Press, 2007.

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8

van, Langevelde Frank, ed. Resource Ecology: Spatial and Temporal Dynamics of Foraging. Dordrecht: Springer Netherlands, 2008.

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9

M, Reilly Stephen, McBrayer Lance D, and Miles Donald B, eds. Lizard ecology: The evolutionary consequences of foraging mode. Cambridge: Cambridge University Press, 2007.

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10

1963-, Miller Lynne E., ed. Eat or be eaten: Predator sensitive foraging among primates. Cambridge, U.K: Cambridge University Press, 2002.

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11

Miller, Lynne E. Eat or be eaten: Predator sensitive foraging among primates. Cambridge, UK: Cambridge University Press, 2002.

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12

Nowacek, Douglas Paul. Sound use, sequential behavior and ecology of foraging bottlenose dolphins, Tursiops truncatus. Cambridge, Mass: Massachusetts Institute of Technology, 1999.

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13

author, Ben-Gal Irad, ed. Search and foraging: Individual motion and swarm dynamics. Boca Raton, FL: CRC Press, 2015.

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14

Viswanathan, Gandhimohan M. The physics of foraging: An introduction to random searches and biological encounters. Cambridge: Cambridge University Press, 2011.

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15

Robinson, John G. Seasonal variation in use of time and space by the wedge-capped capuchin monkey, Cebus olivaceus: Implications for foraging theory. City of Washington: Smithsonian Institution Press, 1986.

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16

Cooper Ornithological Society. International Symposium. Avian foraging: Theory, methodology, and applications : proceedings of an International Symposium of the Cooper Ornithological Society held at Asilomar, California, December 18-19, 1988. Edited by Morrison Michael L and Cooper Ornithological Society. Los Angeles, CA: The Society, 1990.

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17

Andrew, Whiten, and Widdowson Elsie M. 1906-, eds. Foraging strategies and natural diet of monkeys, apes, and humans: Proceedings of a Royal Society Discussion Meeting held on 30 and 31 May 1991. Oxford: Clarendon Press, 1992.

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18

Hughes, R. N. Diet Selection: An Interdisciplinary Approach to Foraging Behaviour. Blackwell Publishing Limited, 1993.

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19

Hughes, R. Diet Selection: An Interdisciplinary Approach to Foraging Behaviour. Wiley & Sons, Incorporated, John, 2009.

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20

Wyatt, Tristram D. 3. How behaviour develops. Oxford University Press, 2017. http://dx.doi.org/10.1093/actrade/9780198712152.003.0003.

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Behaviours evolve by natural selection. As genes influence how behaviours develop, selection on behaviour will alter gene frequencies in subsequent generations: genes that lead to successful behaviours in foraging, parental care, or mate choice, for example, will be represented in more individuals in future generations. If conditions change, then mutations of the genes that give rise to advantageous behaviours will be favoured by selection. ‘How behaviour develops’ explains that the environment is equally important: both genes and environment are intimately and interactively involved in behaviour development. Behavioural imprinting is also discussed along with co-opting genes, gene regulation, social influences on brain gene expression, phenotypic plasticity, and play.
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21

Litvak, Matthew Kenneth. Predator avoidance, foraging behaviour and social transmission of information in fish shoals. 1990.

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22

McMartin, Donald William. Impact of insecticide applications on the foraging behaviour and diet of three boreal forest warbler species. 1996.

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23

Laverty, Terence Mortimer. On the ecological significance of floral complexity and its effect on the foraging behaviour of bumble bees (Hymenoptera: Apidae). 1985.

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24

Foraging behavior. New York: Plenum Press, 1987.

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25

Kamil, A. C. Foraging Behavior. Springer, 2011.

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26

Pulliam, H. R., J. R. Krebs, and A. C. Kamil. Foraging Behavior. Springer, 2012.

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27

Foraging Behavior. Springer, 2013.

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28

Estes, James A., M. Tim Tinker, and Terrie M. Williams. Advances in understanding the physiology, behaviour, and ecology of sea otters. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198759805.003.0023.

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Sea otters are the only fully marine-living mustelid and the smallest extant marine mammal. They have the highest mass-specific metabolic rate of any marine mammal, which coupled with the lack of blubber for insulator and energy storage, relegates them to operating as an extreme income strategist, and appears to have led to a life history tactic in which pregnancy rate is fixed while reproductive success varies with the mother’s body condition at the time of birth, which triggers a decision immediately post-partum to care for or abandon her pup. When resources are limiting, sea otters assume highly individualized diets, which are inherited matrilineally. Sea otters exert strong limiting influences on their macroinvertebrate prey, leading to far reaching indirect effects on the structure and function of coastal marine ecosystems. This chapter reviews and synthesizes the interplay between sea otter energetics and life histories, diet and foraging behaviour, and ecosystem influences.
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29

Ydenberg, Ronald C., Joel S. Brown, and David W. Stephens. Foraging: Behavior and Ecology. University of Chicago Press, 2010.

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30

(Editor), David W. Stephens, Joel S. Brown (Editor), and Ronald C. Ydenberg (Editor), eds. Foraging: Behavior and Ecology. University Of Chicago Press, 2007.

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31

(Editor), David W. Stephens, Joel S. Brown (Editor), and Ronald C. Ydenberg (Editor), eds. Foraging: Behavior and Ecology. University Of Chicago Press, 2007.

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32

(Editor), David W. Stephens, Joel S. Brown (Editor), and Ronald C. Ydenberg (Editor), eds. Foraging: Behavior and Ecology. University Of Chicago Press, 2007.

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33

(Editor), David W. Stephens, Joel S. Brown (Editor), and Ronald C. Ydenberg (Editor), eds. Foraging: Behavior and Ecology. University Of Chicago Press, 2007.

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34

Foraging. Hillsdale, N.J: Lawrence Erlbaum Associates, 1987.

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35

Okasha, Samir. Risk, Rational Choice, and Evolution. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198815082.003.0009.

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Decision-theoretic ideas arise in two areas of biology: risk-sensitive foraging, and the theory of evolution in variable environments. The former concerns the actual behavioural choices that organisms make, the latter the ‘choices’ made by natural selection. A natural suggestion is that both sorts of choices can be modelled in terms of expected utility maximization, the standard theory of rational decision in the face of risk. However, this is only true under particular model assumptions; it does not hold in situations involving a combination of aggregate and idiosyncratic risk. Mixed strategies further complicate the relation between rational and biologically optimal risk preferences. This implies a limit on the validity of the organism-as-rational-agent heuristic as a tool for understanding evolved behaviour.
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36

Giraldeau, Luc-Alain, and Thomas Caraco. Social Foraging Theory. Princeton University Press, 2018.

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37

Giraldeau, Luc-Alain, and Thomas Caraco. Social Foraging Theory. Princeton University Press, 2000.

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38

Shettleworth, Sara J., Michael L. Commons, and Alejandro Kacelnik. Foraging: Quantitative Analyses of Behavior, Volume Vi. Taylor & Francis Group, 2013.

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39

Shettleworth, Sara J., Michael L. Commons, and Alejandro Kacelnik. Foraging: Quantitative Analyses of Behavior, Volume Vi. Taylor & Francis Group, 2013.

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40

Malloy, Cameron. Honeybees: Foraging Behavior, Reproductive Biology and Diseases. Nova Science Publishers, Incorporated, 2014.

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41

Shettleworth, Sara J., Michael L. Commons, and Alejandro Kacelnik. Foraging: Quantitative Analyses of Behavior, Volume Vi. Taylor & Francis Group, 2013.

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42

Shettleworth, Sara J., Michael L. Commons, and Alejandro Kacelnik. Foraging: Quantitative Analyses of Behavior, Volume Vi. Taylor & Francis Group, 2013.

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43

Social Foraging Theory. Princeton University Press, 2000.

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44

Blanckenhorn, Wolf U. Behavioral, plastic, and evolutionary responses to a changing world. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198797500.003.0019.

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Organisms can respond to environmental change by modifying their behavior to obtain an instant response, through short-term phenotypically plastic, often physiological, adjustments, and/or by adapting their life history through a more long-term evolutionary response. Behavioural and physiological responses, in fact, can occur at all these three temporal scales. Examples of behaviors so affected include congregation, dispersal, foraging, migration, or mating. Such responses have consequences at the population and community levels, and ultimately for the evolution of species. This chapter discusses insect examples of these kinds, with an emphasis on human-induced factors, such as (primarily) climate change, pollution, fragmentation, and urbanization.
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45

Foraging: Quantitative Analyses of Behavior, Volume Vi (Quantitative Analyses of Behavior). Lawrence Erlbaum, 1987.

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46

Martin, Graham R. From Senses to Sensory Ecology. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780199694532.003.0005.

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The sensory information available to birds differs markedly between species and it is important to make sense of this diversity in the context of the species’ ecology and behaviour. It is clear that sensory information varies in relation to the environmental challenges that birds face in conducting their lives in different environments, especially with respect to the tasks associated with foraging. Applying knowledge of sensory systems and sensory capacities to questions about how birds are able to carry out particular tasks, especially in environments where information is restricted, provides valuable insights into how bird behaviour is governed by information. By delving into the details of these different sensory worlds, and by exploring their links with specific environments and tasks, we can gain valuable insights into how our human world is also a product of specialised sensory information, which has also evolved for the control of particular tasks in specific types of environmental situations.
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47

Rosati, Alexandra G. Ecological variation in cognition: Insights from bonobos and chimpanzees. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198728511.003.0011.

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Bonobos and chimpanzees are closely related, yet they exhibit important differences in their wild socio-ecology. Whereas bonobos live in environments with less seasonal variation and more access to fallback foods, chimpanzees face more competition over spatially distributed, variable resources. This chapter argues that bonobo and chimpanzee cognition show psychological signatures of their divergent wild ecology. Current evidence shows that despite strong commonalities in many cognitive domains, apes express targeted differences in specific cognitive skills critical for wild foraging behaviours. In particular, bonobos exhibit less accurate spatial memory, reduced levels of patience and greater risk aversion than do chimpanzees. These results have implications for understanding the evolution of human cognition, as studies of apes are a critical tool for modelling the last common ancestor of humans with nonhuman apes. Linking comparative cognition to species’ natural foraging behaviour can begin to address the ultimate reason for why differences in cognition emerge across species. Les bonobos et les chimpanzés sont prochement liés, pourtant ils montrent d’importantes différences dans leur sociologie naturelle. Alors que les bonobos vivent dans des environnements avec peu de diversité de climat entre saisons et plus d’accès à des ressources de nourriture alternatives, les chimpanzés ménagent une compétition étalée spatialement et des ressources plus variées. Je soutiens que la cognition des chimpanzés et bonobos montre les signatures psychologiques de leur écologie naturelle divergente. Les témoignages courants montrent que, malgré les forts points communs dans en cognition, les grands singes expriment des différences au niveau de compétences cognitives importantes au butinage. En particulier, les bonobos démontrent une mémoire spatial moin précise, moin de patience, et plus d’aversion de risques que les chimpanzés. Ces résultats fournissent des signes dans l’étude de l’évolution de la cognition humaine. Les études des grands singe sont un outil d’importance majeure dans la modélisation du dernier ancêtre commun des humains et grands singes non-humains. Faire des liens cognitives comparatives entre le butinage des différentes espèces peut commencer à dévoiler les raisons pour les différences de cognition entre espèces.
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48

Purdy, John. Foraging Behavior of the Honey Bee (Apis Mellifera, L. ). Elsevier Science & Technology Books, 2023.

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49

Foraging behavior and morphology in the avian genus Myrmotherula. 1990.

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50

Pirolli, Peter L. T. Information Foraging Theory: Adaptive Interaction with Information. Oxford University Press, 2009.

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