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Books on the topic 'Social foraging'

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1

K, Earle Timothy, ed. The evolution of human societies: From foraging group to agrarian state. Stanford, Calif: Stanford University Press, 1987.

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2

K, Earle Timothy, ed. The evolution of human societies: From foraging group to agrarian state. 2nd ed. Stanford, Calif: Stanford University Press, 2000.

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3

N, Schmitt Dave, ed. Buzz-Cut Dune and Fremont foraging at the margin of horticulture. Salt Lake City: University of Utah Press, 2004.

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4

Fishing, foraging and farming in the Bolivian Amazon: On a local society in transition. Dordrecht: Springer, 2010.

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5

The principle of sharing: Segregation and construction of social identities at the transition from foraging to farming : proceedings of a symposium held on 29th-31st January 2009 at the Albert-Ludwigs-University of Freiburg, hosted by the Department of Near Eastern Archaeology. Berlin: Ex Oriente, 2010.

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6

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

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7

Social Foraging Theory. Princeton University Press, 2000.

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8

Kelly, Robert L. Lifeways of Hunter-Gatherers: The Foraging Spectrum. Cambridge University Press, 2013.

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9

Kelly, Robert L. Lifeways of Hunter-Gatherers: The Foraging Spectrum. Cambridge University Press, 2013.

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10

Bushmen Of Southern Africa: Foraging Society In Transition. Ohio University Press, 2000.

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11

Evolution of Human Societies: From Foraging Group to Agrarian State. Stanford University Press, 1988.

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12

Johnson, Allen W., and Timothy K. Earle. Evolution of Human Societies: From Foraging Group to Agrarian State. Stanford University Press, 2000.

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13

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

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14

Habu, Junko, and Ben Fitzhugh. Beyond Foraging and Collecting: Evolutionary Change in Hunter-Gatherer Settlement Systems. Springer, 2012.

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15

From Foraging To Farming In The Andes New Perspectives On Food Production And Social Organization. Cambridge University Press, 2011.

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16

From Foraging to Farming in the Andes: New Perspectives on Food Production and Social Organization. University of Cambridge ESOL Examinations, 2014.

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17

Edwards, Thomas C. Temporal and social aspects of the foraging ecology of a piscivore, the osprey (Pandion haliaetus). 1987.

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18

Ringhofer, Lisa. Fishing, Foraging and Farming in the Bolivian Amazon: On a Local Society in Transition. Springer, 2014.

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19

Schulkin, Jay. Social Contact, Gonadal Steroids, and CRF. Oxford University Press, 2017. http://dx.doi.org/10.1093/acprof:oso/9780198793694.003.0006.

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Chapter 6 begins with a brief discussion of CRF in approach/avoidance behaviors across pre- and postnatal events. What will follow is the description of diverse steroids, in particular gonadal steroids (e.g., testosterone and estrogen) and their effect on CRF and other peptides expression, and finally, sex differences in the expression of CRF in the brain. Importantly, the rapid-fire expression of CRF would serve essential for differing social/ecological demands: parenting is one; responding to conspecifics is another. What evolved is a CRF signature ready for action, responding to changing demands of importance, part of the neural armor in foraging for coherence.
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20

(Editor), Ben Fitzhugh, and Junko Habu (Editor), eds. Beyond Foraging and Collecting: Evolutionary Change in Hunter-Gatherer Settlement Systems (Fundamental Issues in Archaeology). Springer, 2002.

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21

Schmitt, Dave N., and David Madsen. Buzz-Cut Dune And Fremont Foraging at the Margin of Horticulture (University of Utah Anthropological Paper). University of Utah Press, 2005.

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22

Sterelny, Kim. The Pleistocene Social Contract. Oxford University Press, 2021. http://dx.doi.org/10.1093/oso/9780197531389.001.0001.

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No human now gathers for himself or herself the essential resources for life: food, shelter, clothing and the like. Humans are obligate co-operators, and this has been true for tens of thousands of years; probably much longer. In this regard, humans are very unusual. In the living world more generally, cooperation outside the family is rare. Though it can be very profitable, it is also very risky, as cooperation makes an agent vulnerable to incompetence and cheating. This book presents a new picture of the emergence of cooperation in our lineage, developing through four fairly distinct phases. Our trajectory began from a baseline that was probably fairly similar to living great apes, who cooperate, but in fairly minimal ways. As adults, they rarely depend on others when the outcome really matters. This book suggests that cooperation began to be more important for humans through an initial phase of cooperative foraging generating immediate returns from collective action in small mobile bands. This established in our lineage about 1.8 million years ago, perhaps earlier. Over the rest of the Pleistocene, cooperation became more extended in its social scale, with forms of cooperation between bands gradually establishing, and in spatial and temporal scale too, with various forms of reciprocation becoming important. The final phase was the emergence of cooperation in large scale, hierarchical societies in the Holocene, beginning about 12,000 years ago. This picture is nested in a reading of the archaeological and ethnographic record, and twinned to an account of the gradual elaboration of cultural learning in our lineage, making cooperation both more profitable and more stable.
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23

Fewell, Jennifer, and Patrick Abbot. Sociality. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198797500.003.0015.

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This chapter examines the different types of social forms found in insect taxa, from the relatively simple social behaviors of aggregating species, to the complex cooperative and altruistic interactions that frame cohesive communal and eusocial groups. The diverse patterns of insect social living are considered within an inclusive fitness framework, to explore the fundamental question of why social species can be so successful, but sociality itself is taxonomically rare. To answer this question requires consideration of the ecological, life history and behavioral drivers of social living, including the roles of cooperative group defence, alloparental care, cooperative foraging, and group homeostasis. The evolution of cooperative sociality does not form a single path from group living to eusociality. Instead, its diverse forms represent different evolutionary solutions to those ecological problems that can best be solved by living socially.
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24

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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25

Bar-Yosef, Ofer, Miryam Bar-Matthews, and Avner Ayalon. 12,000–11,700 cal BP. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780199329199.003.0002.

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We take up the question of “why” cultivation was adopted by the end of the Younger Dryas by reviewing evidence in the Levant, a sub-region of southwestern Asia, from the Late Glacial Maximum through the first millennium of the Holocene. Based on the evidence, we argue that the demographic increase of foraging societies in the Levant at the Terminal Pleistocene formed the backdrop for the collapse of foraging adaptations, compelling several groups within a particular “core area” of the Fertile Crescent to become fully sedentary and introduce cultivation alongside intensified gathering in the Late Glacial Maximum, ca. 12,000–11,700 cal BP. In addition to traditional hunting and gathering, the adoption of stable food sources became the norm. The systematic cultivation of wild cereals begun in the northern Levant resulted in the emergence of complex societies across the entire Fertile Crescent within several millennia. Results of archaeobotanical and archaeozoological investigations provide a basis for reconstructing economic strategies, spatial organization of sites, labor division, and demographic shifts over the first millennium of the Holocene. We draw our conclusion from two kinds of data from the Levant, a sub-region of southwestern Asia, during the Terminal Pleistocene and early Holocene: climatic fluctuations and the variable human reactions to natural and social calamities. The evidence in the Levant for the Younger Dryas, a widely recognized cold period across the northern hemisphere, is recorded in speleothems and other climatic proxies, such as Dead Sea levels and marine pollen records.
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26

Verschure, Paul F. M. J. A chronology of Distributed Adaptive Control. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780199674923.003.0036.

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This chapter presents the Distributed Adaptive Control (DAC) theory of the mind and brain of living machines. DAC provides an explanatory framework for biological brains and an integration framework for synthetic ones. DAC builds on several themes presented in the handbook: it integrates different perspectives on mind and brain, exemplifies the synthetic method in understanding living machines, answers well-defined constraints faced by living machines, and provides a route for the convergent validation of anatomy, physiology, and behavior in our explanation of biological living machines. DAC addresses the fundamental question of how a living machine can obtain, retain, and express valid knowledge of its world. We look at the core components of DAC, specific benchmarks derived from the engagement with the physical and the social world (the H4W and the H5W problems) in foraging and human–robot interaction tasks. Lastly we address how DAC targets the UTEM benchmark and the relation with contemporary developments in AI.
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27

Russ, Jon, ed. Bat Calls of Britain and Europe. Pelagic Publishing, 2021. http://dx.doi.org/10.53061/nlhc3923.

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A comprehensive guide to the calls of the 44 species of bat currently known to occur in Europe. Following on from the popular British Bat Calls by Jon Russ, this new book draws on the expertise of more than forty specialist authors to substantially update all sections, further expanding the volume to include sound analysis and species identification of all European bats. Aimed at volunteers and professional alike, topics include the basics of sound, echolocation in bats, an introduction to acoustic communication, equipment used and call analysis. For each species, detailed information is given on distribution, emergence, flight and foraging behaviour, habitat, echolocation calls – including parameters of common measurements – and social calls. Calls are described for both heterodyne and time expansion/full spectrum systems. A simple but complete echolocation guide to all species is provided for beginners, allowing them to analyse call sequences and arrive at the most likely species or group. The book also includes access to a downloadable library of over 450 calls presented as sonograms in the species sections.
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28

Call, Josep. Bonobos, chimpanzees and tools: Integrating species-specific psychological biases and socio-ecology. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198728511.003.0012.

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Over the years there has been some controversy regarding the comparison between chimpanzees and bonobos. Whereas some authors have stressed their differences, others have stressed their similarities. One striking difference between wild chimpanzees and bonobos is tool use, especially in foraging contexts. While several chimpanzee populations possess tool kits formed by multiple tools (and their associated techniques) to exploit embedded resources, bonobos display no such tool specialization. However, studies in the laboratory have shown that bonobos are perfectly capable of using tools. In fact, several studies devoted to investigate the cognitive abilities underlying tool use have failed to detect any substantial differences between the two species. This chapter explores three aspects that could explain the difference between chimpanzees and bonobos in their propensity to use tools in the wild: socio-ecological factors, social versus technical cognition, and personality profiles. Au cours du temps, il y a eu beaucoup de controverse en relation aux comparaisons entres les chimpanzés et les bonobos. Alors que certains auteurs ont stressé les différences entre eux, d’autres ont stressé les similarités. Une grande différence entre les chipmanzés et les bonobos sauvages est l’utilisation des outils, spécialement en butinage. Tandis que plusieurs populations de chimpanzés possèdent des boîtes à outils diverses (et leur techniques respectives) pour exploiter les ressources, les bonobos ne montrent pas une spécialisation pareille. Cependant, les études en laboratoir ont montré que les bonobos sont capables d’utiliser des outils. En faite, plusieurs études des facultés cognitives dans l’utilisation des outils n’ont pas pu détecter de différences substantielles entre les deux espèces. Je vais explorer trois aspects qui pourraient expliquer les différences entre les chimpanzés et les bonobos en ce qui concerne leur tendance naturelle à utiliser les outils: facteurs socio-écologiques, cognition social vs. technique, et profils de personnalité.
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29

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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30

Weiss, Harvey. Megadrought, Collapse, and Causality. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780199329199.003.0001.

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Recent discoveries of megadroughts, severe periods of drought lasting decades or centuries, during the course of the Holocene have revolutionized our understanding of modern climate history. Through advances in paleoclimatology, researchers have identified these periods of climate change by analyzing high-resolution proxy data derived from lake sediment cores, marine cores, glacial cores, speleothem cores, and tree rings. Evidence that megadroughts occurred with frequency and abruptly over the last 12,000 years, a timespan long assumed to be stable compared to earlier glacial periods, has also altered our understanding of societies’ trajectories. The fact that severe, multi-decadal or century-scale droughts coincided with societal collapses well known to archaeologists has challenged established multi-causal analyses of these events. Megadroughts, impossible to predict and impossible to withstand, may have caused political collapse, regional abandonment, and habitat tracking to still-productive regions. The nine megadrought and societal collapse events presented in this volume extend from the foraging-to-agriculture transition at the dawn of the Holocene in West Asia to the fifteenth-century AD collapse of the Khmer Empire in Angkor (Cambodia). Inevitably, this collection of essays also raises challenges to causal analyses of societal collapse and for future paleoclimatic and archaeological research.
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31

Tong, Wenfei. How Birds Behave. CSIRO Publishing, 2020. http://dx.doi.org/10.1071/9781486313297.

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Birds are intelligent, sociable creatures that exhibit a wide array of behaviours – from mobbing and mimicking to mating and joint nesting. Why do they behave as they do? Bringing to light the remarkable actions of birds through examples from species around the world, How Birds Behave presents engaging vignettes about the private lives of birds, all explained in an evolutionary context. We discover how birds find food, relying on foraging techniques, tools and thievery. We learn about the courtship rituals through which birds choose, compete for, woo and win mates; the familial conflicts that crop up among parents, offspring and siblings; and the stresses and strains of nesting, including territory defence, nepotism and relationship sabotage. We see how birds respond to threats and danger – through such unique practices as murmurations, specific alarm calls, distraction displays and antipredator nest design. We also read about how birds change certain behaviours – preening, migration, breeding and huddling – based on climate. Richly illustrated, this book explores the increasing focus on how individual birds differ in personality and how big data and citizen scientists are helping to add to what we know about them. Drawing on classic examples and the latest research, How Birds Behave offers a close-up look at the many ways birds conduct themselves in the wild.
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