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  1. Eshkol-Wachman movement notation and the evolution of locomotor patterns in vertebrates.Robert C. Eaton - 1992 - Behavioral and Brain Sciences 15 (2):272-274.
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  • Is the mobility gradient suitable for general application?George W. Barlow - 1992 - Behavioral and Brain Sciences 15 (2):267-268.
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  • Human observation and human action.Darren Newtson - 1992 - Behavioral and Brain Sciences 15 (2):285-285.
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  • From psychopharmacology to neuropsychopharmacology: Adapting behavioral terminology to neural events.George V. Rebec - 1992 - Behavioral and Brain Sciences 15 (2):287-288.
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  • Joint torque precedes the kinematic end result.William A. MacKay - 1992 - Behavioral and Brain Sciences 15 (2):283-284.
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  • The mobility gradient from a comparative phylogenetic perspective.David Eilam - 1992 - Behavioral and Brain Sciences 15 (2):274-275.
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  • Do grooming and speech really serve homologous functions?Merlin Donald - 1993 - Behavioral and Brain Sciences 16 (4):700-701.
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  • Sensorimotor reference frames and physiological attractors.René Thom - 1992 - Behavioral and Brain Sciences 15 (2):289-289.
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  • Structure and function in the CNS.Peter H. Klopfer - 1992 - Behavioral and Brain Sciences 15 (2):281-282.
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  • 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.
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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.
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  • Confounded correlations, again.Terrence W. Deacon - 1993 - Behavioral and Brain Sciences 16 (4):698-699.
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  • Time-based objective coding and human nonverbal behavior.Roger D. Masters - 1992 - Behavioral and Brain Sciences 15 (2):284-285.
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  • Comparative studies, phylogenies and predictions of coevolutionary relationships.Emília P. Martins - 1993 - Behavioral and Brain Sciences 16 (4):714-716.
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  • 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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  • Fairness as a Moral Grounding for Space Policy.James S. J. Schwartz - 2014 - In Charles S. Cockell (ed.), The Meaning of Liberty Beyond Earth. Cham: Springer.
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  • 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.
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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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  • Number our days: Quantifying social evolution.Harry J. Jerison - 1993 - Behavioral and Brain Sciences 16 (4):712-713.
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  • Behavioural constraints on social communication are not likely to prevent the evolution of large social groups in nonhuman primates.R. J. Andrew - 1993 - Behavioral and Brain Sciences 16 (4):694-694.
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  • What are voluntary movements made of?Ian Q. Whishaw - 1992 - Behavioral and Brain Sciences 15 (2):290-291.
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  • Somewhere in time – temporal factors in vertebrate movement analysis.Melvin Lyon - 1992 - Behavioral and Brain Sciences 15 (2):282-283.
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  • Describing behavior: A new label for an old wine?Wolfgang M. Schleidt - 1992 - Behavioral and Brain Sciences 15 (2):288-289.
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  • 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.
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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.
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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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  • Dynamical systems theory and the mobility gradient: Information, homology and self-similar structure.Gary Goldberg - 1992 - Behavioral and Brain Sciences 15 (2):278-279.
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  • The mobility gradient: Useful, general, falsifiable?John A. Byers - 1992 - Behavioral and Brain Sciences 15 (2):270-271.
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  • Group size, language and evolutionary mechanisms.Harold Kincaid - 1993 - Behavioral and Brain Sciences 16 (4):713-714.
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  • Vocal grooming: Man the schmoozer.David Dean - 1993 - Behavioral and Brain Sciences 16 (4):699-700.
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  • Mosaic evolution of the neocortex.Dean Falk & Bruce Dudek - 1993 - Behavioral and Brain Sciences 16 (4):701-702.
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  • Do larger brains mean greater intelligence?R. W. Byrne - 1993 - Behavioral and Brain Sciences 16 (4):696-697.
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  • Moving beyond words.Robert Fagen - 1992 - Behavioral and Brain Sciences 15 (2):275-276.
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  • A developmental look at grooming, grunting and group cohesion.Lorraine McCune - 1993 - Behavioral and Brain Sciences 16 (4):716-717.
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  • The environment modulates the mobility gradient, temporally if not sequentially.Charles H. M. Beck - 1992 - Behavioral and Brain Sciences 15 (2):268-269.
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  • Brains, grouping and language.A. H. Harcourt - 1993 - Behavioral and Brain Sciences 16 (4):706-706.
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  • Radiators and big brains in walkie-talkie primates.Martin Pickford - 1991 - Behavioral and Brain Sciences 14 (3):528-529.
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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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  • Grooming and language as cohesion mechanisms: Choosing the right data.Marina Cords - 1993 - Behavioral and Brain Sciences 16 (4):697-698.
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  • Brain expansion: Thoughts on hunting or reckoning kinship – or both?C. Loring Brace - 1993 - Behavioral and Brain Sciences 16 (4):695-696.
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  • 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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  • 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.
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  • 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.
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  • Do gossip and lack of grooming make us human?Ilya I. Glezer & Warren G. Kinzey - 1993 - Behavioral and Brain Sciences 16 (4):704-705.
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  • A gesture in the right direction?Michael C. Corballis - 1993 - Behavioral and Brain Sciences 16 (4):697-697.
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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.
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  • 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.
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  • Paleoclimatic Variation and Brain Expansion during Human Evolution.Jessica Ash & Gordon G. Gallup - 2007 - Human Nature 18 (2):109-124.
    One of the major adaptations during the evolution of Homo sapiens was an increase in brain size. Here we present evidence that a significant and substantial proportion of variation in brain size may be related to changes in temperature. Based on a sample of 109 fossilized hominid skulls, we found that cranial capacities were highly correlated with paleoclimatic changes in temperature, as indexed by oxygen isotope data and sea-surface temperature. Indeed, as much as 52% of the variance in the cranial (...)
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  • Testing for controlled variables.William T. Powers - 1992 - Behavioral and Brain Sciences 15 (2):286-287.
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  • Ecological and social variance and the evolution of increased neocortical size.R. A. Foley - 1993 - Behavioral and Brain Sciences 16 (4):702-703.
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