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  1. Another primate brain fiction: Brain (cortex) weight and homogeneity.Ralph L. Holloway - 1993 - Behavioral and Brain Sciences 16 (4):707-708.
  • Did primates need more than social grooming and increased group size for acquiring language?Jan Wind - 1993 - Behavioral and Brain Sciences 16 (4):720-720.
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  • What are voluntary movements made of?Ian Q. Whishaw - 1992 - Behavioral and Brain Sciences 15 (2):290-291.
  • Social complexity: The roles of primates' grooming and people's talking.Andrew Whiten - 1993 - Behavioral and Brain Sciences 16 (4):719-719.
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  • Birdsong: Variations that follow rules.Dietmar Todt & Henrike Hultsch - 1992 - Behavioral and Brain Sciences 15 (2):289-290.
  • Sensorimotor reference frames and physiological attractors.René Thom - 1992 - Behavioral and Brain Sciences 15 (2):289-289.
  • The rest of the story: Grooming, group size and vocal exchanges in neotropical primates.Charles T. Snowdon - 1993 - Behavioral and Brain Sciences 16 (4):718-718.
  • Grooming is not the only regulator of primate social interactions.Robert M. Seyfarth & Dorothy L. Cheney - 1993 - Behavioral and Brain Sciences 16 (4):717-718.
  • Describing behavior: A new label for an old wine?Wolfgang M. Schleidt - 1992 - Behavioral and Brain Sciences 15 (2):288-289.
  • From psychopharmacology to neuropsychopharmacology: Adapting behavioral terminology to neural events.George V. Rebec - 1992 - Behavioral and Brain Sciences 15 (2):287-288.
  • Testing for controlled variables.William T. Powers - 1992 - Behavioral and Brain Sciences 15 (2):286-287.
  • Radiators and big brains in walkie-talkie primates.Martin Pickford - 1991 - Behavioral and Brain Sciences 14 (3):528-529.
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  • The yin and yang of behavioral analysis.Sergio M. Pellis - 1992 - Behavioral and Brain Sciences 15 (2):286-286.
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  • Human observation and human action.Darren Newtson - 1992 - Behavioral and Brain Sciences 15 (2):285-285.
  • A developmental look at grooming, grunting and group cohesion.Lorraine McCune - 1993 - Behavioral and Brain Sciences 16 (4):716-717.
  • Time-based objective coding and human nonverbal behavior.Roger D. Masters - 1992 - Behavioral and Brain Sciences 15 (2):284-285.
  • Comparative studies, phylogenies and predictions of coevolutionary relationships.Emília P. Martins - 1993 - Behavioral and Brain Sciences 16 (4):714-716.
  • Joint torque precedes the kinematic end result.William A. MacKay - 1992 - Behavioral and Brain Sciences 15 (2):283-284.
  • Somewhere in time – temporal factors in vertebrate movement analysis.Melvin Lyon - 1992 - Behavioral and Brain Sciences 15 (2):282-283.
  • Animal motility: Gestalt or piecemeal assembly.Paul Leyhausen - 1992 - Behavioral and Brain Sciences 15 (2):282-282.
  • Structure and function in the CNS.Peter H. Klopfer - 1992 - Behavioral and Brain Sciences 15 (2):281-282.
  • Group size, language and evolutionary mechanisms.Harold Kincaid - 1993 - Behavioral and Brain Sciences 16 (4):713-714.
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  • Number our days: Quantifying social evolution.Harry J. Jerison - 1993 - Behavioral and Brain Sciences 16 (4):712-713.
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  • Hunter-gatherer sociospatial organization and group size.Robert Jarvenpa - 1993 - Behavioral and Brain Sciences 16 (4):712-712.
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  • Primate group size, brains and communication: A New World perspective.Charles H. Janson - 1993 - Behavioral and Brain Sciences 16 (4):711-712.
  • Sizing up social groups.Bob Jacobs & Michael J. Raleigh - 1993 - Behavioral and Brain Sciences 16 (4):710-711.
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  • Size of human groups during the Paleolithic and the evolutionary significance of increased group size.Michael E. Hyland - 1993 - Behavioral and Brain Sciences 16 (4):709-710.
  • The functions of grooming and language: The present need not reflect the past.Marc Hauser, Leah Gardner, Tony Goldberg & Adrian Treves - 1993 - Behavioral and Brain Sciences 16 (4):706-707.
  • Shapes of behaviour.John G. Harries - 1992 - Behavioral and Brain Sciences 15 (2):279-281.
  • Brains, grouping and language.A. H. Harcourt - 1993 - Behavioral and Brain Sciences 16 (4):706-706.
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  • The historical turn in the study of adaptation.Paul E. Griffiths - 1996 - British Journal for the Philosophy of Science 47 (4):511-532.
    A number of philosophers and ‘evolutionary psychologists’ have argued that attacks on adaptationism in contemporary biology are misguided. These thinkers identify anti-adaptationism with advocacy of non-adaptive modes of explanation. They overlook the influence of anti-adaptationism in the development of more rigorous forms of adaptive explanation. Many biologists who reject adaptationism do not reject Darwinism. Instead, they have pioneered the contemporary historical turn in the study of adaptation. One real issue which remains unresolved amongst these methodological advances is the nature of (...)
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  • Anthropological criticisms of Dunbar's theory of the origin of language.Robert Bates Graber - 1993 - Behavioral and Brain Sciences 16 (4):705-705.
  • The natural geometry of a behavioral homology.Ilan Golani - 1992 - Behavioral and Brain Sciences 15 (2):291-308.
  • Dynamical systems theory and the mobility gradient: Information, homology and self-similar structure.Gary Goldberg - 1992 - Behavioral and Brain Sciences 15 (2):278-279.
  • A mobility gradient in the organization of vertebrate movement: The perception of movement through symbolic language.Ilan Golani - 1992 - Behavioral and Brain Sciences 15 (2):249-266.
  • Do gossip and lack of grooming make us human?Ilya I. Glezer & Warren G. Kinzey - 1993 - Behavioral and Brain Sciences 16 (4):704-705.
  • Group structure and group size among humans and other primates.Linton C. Freeman - 1993 - Behavioral and Brain Sciences 16 (4):703-704.
  • Ecological and social variance and the evolution of increased neocortical size.R. A. Foley - 1993 - Behavioral and Brain Sciences 16 (4):702-703.
  • Uniqueness of human intelligence may be underrated in current estimates.Konrad R. Fialkowski - 1991 - Behavioral and Brain Sciences 14 (3):527-528.
  • Alternative taxonomies in movement: Not only possible but critical.John C. Fentress - 1992 - Behavioral and Brain Sciences 15 (2):277-278.
  • Connecting invertebrate behavior, neurophysiology and evolution with Eshkol-Wachman movement notation.Zen Faulkes & Dorothy Hayman Paul - 1992 - Behavioral and Brain Sciences 15 (2):276-277.
  • Mosaic evolution of the neocortex.Dean Falk & Bruce Dudek - 1993 - Behavioral and Brain Sciences 16 (4):701-702.
  • More on the radiator.Dean Falk - 1991 - Behavioral and Brain Sciences 14 (3):529-530.
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  • Moving beyond words.Robert Fagen - 1992 - Behavioral and Brain Sciences 15 (2):275-276.
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  • The mobility gradient from a comparative phylogenetic perspective.David Eilam - 1992 - Behavioral and Brain Sciences 15 (2):274-275.
  • Eshkol-Wachman movement notation and the evolution of locomotor patterns in vertebrates.Robert C. Eaton - 1992 - Behavioral and Brain Sciences 15 (2):272-274.
  • On the origins of language: A history of constraints and windows of opportunity.R. I. M. Dunbar - 1993 - Behavioral and Brain Sciences 16 (4):721-735.
  • Coevolution of neocortical size, group size and language in humans.R. I. M. Dunbar - 1993 - Behavioral and Brain Sciences 16 (4):681-694.
    Group size is a function of relative neocortical volume in nonhuman primates. Extrapolation from this regression equation yields a predicted group size for modern humans very similar to that of certain hunter-gatherer and traditional horticulturalist societies. Groups of similar size are also found in other large-scale forms of contemporary and historical society. Among primates, the cohesion of groups is maintained by social grooming; the time devoted to social grooming is linearly related to group size among the Old World monkeys and (...)
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  • Language and levels of selection.Lee Alan Dugatkin & David Sloan Wilson - 1993 - Behavioral and Brain Sciences 16 (4):701-701.
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  • Do grooming and speech really serve homologous functions?Merlin Donald - 1993 - Behavioral and Brain Sciences 16 (4):700-701.