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McGreevy, P.D. |
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2004 |
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Equine Behavior: A Guide for Veterinarians and Equine Scientists |
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Cited By (since 1996): 25; Export Date: 21 October 2008 |
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Equine Behaviour @ team @ |
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4530 |
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McLean, A.N. |
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The mental processes of the horse and their consequences for training |
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2004 |
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Animal Welfare Science Centre |
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Cited By (since 1996): 1; Export Date: 24 October 2008 |
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Admin @ knut @ |
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4619 |
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Kleiven, J.; Bjerke, T.; Kaltenborn, B.P. |
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Factors influencing the social acceptability of large carnivore behaviours |
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2004 |
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Biodivers Conserv |
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13 |
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Equine Behaviour @ team @ Kleiven2004 |
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6447 |
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Apollonio, M.; Mattioli, L.; Scandura, M.; Mauri, L.; Gazzola, A.; Avanzinelli, E. |
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Wolves in the Casentinesi Forests: insights for wolf conservation in Italy from a protected area with a rich wild prey community |
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2004 |
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Biol Conserv |
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120 |
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Equine Behaviour @ team @ Apollonio2004 |
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6475 |
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Author |
Huebener, E. |
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Title |
Die Bewegungen von Pferderumpf und -rücken aus der Sicht des Reiters |
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Journal Article |
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2004 |
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Tierärztliche Umschau |
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Tierärztl. Umschau |
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6 |
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327-334 |
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Schritt – Trab – Galopp – Schmerz – Schäden |
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Die Bewegungen von Rumpf und Rücken des Pferdes in der Fortbewegung bestimmen Sitz und Schenkelhilfen – Grundlagen pferdgerechten und kultivierten, feinfühligen Reitens. In ihrer Tendenz ließen sich diese Bewegungen jetzt aus den Fußfolgen der Grundgangarten ableiten. Die Erkenntnisse sind per Video verifiziert. Mit ihrer Übersetzung in Diagramme wurde versucht, den gegenwärtigen Wissensstand für nicht-reitende Wissenschaftler und denkende Reiter gleichermaßen verständlich darzustellen. Die Akzeptanz des aufbereiteten Wissens in der Reiterei würde verbessert, wenn man zu gemessenen Werten für die Bewegungen des Pferderückens und des Pferderumpfes käme. Plädoyer eines “Nur-Reiters” für einschlägige, universitäre Forschung. |
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German |
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refbase @ user @ |
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420 |
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Author |
Huebener, E. |
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Title |
Movements of Trunk and Back of the Horse from a Rider's View |
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2004 |
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Tierärztliche Umschau |
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Tierärztl. Umschau |
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6 |
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327 |
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walk – trot – canter – pain – damages |
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The trunk and back movements of the horse during locomotion determine seat position and leg aids of the rider, this is the basis for horse-oriented and cultivated, sensitive riding. In their tendency these movements could now be derived from the foot sequences of the basic paces. The realizations are verified by video. By translating these movements into diagrams, the author is making an attempt to present the current state of knowledge for non-riding scholars and academically oriented riders alike. The acceptance of the prepared riding knowledge would be improved if one could produce measured values of the horse's back and trunk movements. An appeal of a rider for relevant, scholarly research. |
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German |
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refbase @ user @ |
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437 |
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Author |
Dall, Sasha R. X; Houston, Alasdair I.; McNamara, John M. |
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Title |
The behavioural ecology of personality: consistent individual differences from an adaptive perspective |
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2004 |
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Ecology Letters |
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Ecol. Letters |
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7 |
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734-739 |
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Adaptive individual differences, behavioural ecology, behavioural syndromes, evolutionary game theory, life history strategies, personality differences, state-dependent dynamic programming |
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Abstract |
Individual humans, and members of diverse other species, show consistent differences in
aggressiveness, shyness, sociability and activity. Such intraspecific differences in
behaviour have been widely assumed to be non-adaptive variation surrounding
(possibly) adaptive population-average behaviour. Nevertheless, in keeping with recent
calls to apply Darwinian reasoning to ever-finer scales of biological variation, we sketch
the fundamentals of an adaptive theory of consistent individual differences in behaviour.
Our thesis is based on the notion that such .personality differences. can be selected for if
fitness payoffs are dependent on both the frequencies with which competing strategies
are played and an individual`s behavioural history. To this end, we review existing models
that illustrate this and propose a game theoretic approach to analyzing personality
differences that is both dynamic and state-dependent. Our motivation is to provide
insights into the evolution and maintenance of an apparently common animal trait:
personality, which has far reaching ecological and evolutionary implications. |
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494 |
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Author |
Cheney, D. l .; Seyfarth, R. M. |
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Title |
Social complexity and the information acquired during eavesdropping by primates and other animals |
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2004 |
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Animal Communication networks |
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In many of the studies reviewed in this book, eavesdropping takes the
following form: a subject has the opportunity to monitor, or eavesdrop upon, an
interaction between two other animals,Aand B. The subject then uses the information
obtained through these observations to assess A`s and B`s relative dominance
or attractiveness as a mate (e.g. Mennill et al., 2002; Ch. 2). For example, Oliveira
et al. (1998) found that male fighting fish Betta splendens that had witnessed two
other males involved in an aggressive interaction subsequently responded more
strongly to the loser of that interaction than the winner. Subjects-behaviour could
not have been influenced by any inherent differences between the two males, because
subjects responded equally strongly to the winner and the loser of competitive
interactions they had not observed. Similarly, Peake et al. (2001) presented
male great tits Parus major with the opportunity to monitor an apparent competitive
interaction between two strangers by simulating a singing contest using two
loudspeakers. The relative timing of the singing bouts (as measured by the degree
of overlap between the two songs) provided information about each “contestants”
relative status. Following the singing interaction, one of the “contestants” was
introduced into the male`s territory. Males responded significantly less strongly
to singers that had apparently just “lost” the interaction (see also McGregor &
Dabelsteen, 1996; Naguib et al., 1999; Ch. 2).
What information does an individual acquire when it eavesdrops on others?
In theory, an eavesdropper could acquire information of many different sorts:
about A, about B, about the relationship between A and B, or about the place of
Animal Communication Networks, ed. Peter K. McGregor. Published by Cambridge University Press.
c.
Cambridge University Press 2005.
583
P1: JZZ/... P2: JZZ/...
0521823617c25.xml CU1917B/McGregor 0 521 582361 7 October 7, 2004 22:31
584 D. L. Cheney & R. M. Seyfarth
A`s and B`s relationship in a larger social framework. The exact information acquired
will probably reflect the particular species social structure. For example,
songbirds like great tits live in communities in which six or seven neighbours
surround each territory-holding male. Males appear to benefit from the knowledge
that certain individuals occupy specific areas (e.g. Brooks & Falls, 1975), that
competitive interactions between two different neighbours have particular outcomes,
and that these outcomes are stable over time. We would, therefore, expect
an eavesdropping great tit not only to learn that neighbour A was dominant to
neighbour B, for example, but also to form the expectation that A was likely to
defeat B in all future encounters. More speculatively, because the outcome of territorial
interactions are often site specific (reviewed by Bradbury & Vehrencamp,
1998), we would expect eavesdropping tits to learn further that A dominates B
in some areas but B dominates A in others. In contrast, the information gained
from monitoring neighbours interactions would unlikely be sufficient to allow
the eavesdropper to rank all of its neighbours in a linear dominance hierarchy,
because not all neighbouring males would come into contact with one another.
Such information would be difficult if not impossible to acquire; it might also be
of little functional value.
In contrast, species that live in large, permanent social groups have a much
greater opportunity to monitor the social interactions of many different individuals
simultaneously. Monkey species such as baboons Papio cynocephalus, for
example, typically live in groups of 80 or more individuals, which include several
matrilineal families arranged in a stable, linear dominance rank order (Silk et al.,
1999). Offspring assume ranks similar to those of their mothers, and females maintain
close bonds with their matrilineal kin throughout their lives. Cutting across
these stable long-term relationships based on rank and kinship are more transient
bonds: for example, the temporary associations formed between unrelated
females whose infants are of similar ages, and the “friendships” formed between
adult males and lactating females as an apparent adaptation against infanticide
(Palombit et al., 1997, 2001). In order to compete successfully within such groups, it
would seem advantageous for individuals to recognize who outranks whom, who
is closely bonded to whom, and who is likely to be allied to whom (Harcourt, 1988,
1992; Cheney & Seyfarth, 1990; see below). The ability to adopt a third party`s perspective
and discriminate among the social relationships that exist among others
would seem to be of great selective benefit.
In this chapter, we review evidence for eavesdropping in selected primate
species and we consider what sort of information is acquired when one individual
observes or listens in on the interactions of others. We then compare eavesdropping
by primates with eavesdropping in other animal species, focusing on both
potential differences and directions for further research |
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Cambridge University Press |
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Cambridge, Massachusetts |
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McGregor, P.K. |
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495 |
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Author |
Itakura, S. |
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Title |
Gaze Following and Joint Visual Attention in Nonhuman Animals |
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Journal Article |
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2004 |
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Japanese Psychological Research |
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Jpn. Psychol. Res. |
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3 |
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216-226 |
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gaze-following; joint visual attention; theory of mind; nonhuman animal |
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n this paper, studies of gaze-following and joint visual attention in nonhuman animals are reviewed from the theoretical perspective of Emery (2000). There are many studies of gaze-following and joint visual attention in nonhuman primates. The reports concern not only adult individuals but also the development of these abilities. Studies to date suggest that monkeys and apes are able to follow the gaze of others, but only apes can understand the seeing-knowing relationship with regards to conspecifics in competitive situations. Also, there have recently been some reports of ability to follow the gaze of humans in domestic animals, such as dogs or horses, interacting with humans. These domestic animals are considered to have acquired this ability during their long history of selective breeding by humans. However, we need to clarify social gaze parameters in various species to improve our knowledge of the evolution of how we process others gazing, attention, and mental states. |
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Author |
Galef Jr B.G., |
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Title |
Approaches to the study of traditional behaviors of free-living animals |
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Journal Article |
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2004 |
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Learning & Behavior |
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Learn. Behav. |
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32 |
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53-61 |
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I review literature on four different approaches to the study of traditions in animals: observation of free-living animals, laboratory experiment, armchair analysis, and field experiment. Because, by definition, a tradition entails social learning of some kind, it is difficult, perhaps impossible, to establish that a behavior is in fact traditional without knowledge of how it develops. Observations of free-living animals often provide strong circumstantial evidence of a tradition. However, even in the view of several researchers who have studied possibly traditional behaviors in natural populations, observation alone has not proven sufficient to show that social learning contributes to development of behaviors of interest. The relevance of laboratory experiments to the understanding of the development of behaviors in free-living animals is always open to challenge. Armchair analyses of field data can produce interesting hypotheses but cannot test them. Field experiments to determine how behaviors of interest develop in population members provide a promising way forward. |
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