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Functions of Brain Lateralization :

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Approach before the interaction ... Banya was approached more often from its left visual field. No group-level bias to be approached from one visual field more often. ... – PowerPoint PPT presentation

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Title: Functions of Brain Lateralization :


1
supervisors E. Hogervorst, W. Sellers C.
Blois-Heulin
Amandine Chapelain
Department of Human Sciences, Loughborough
University, LE11 3TU, England
a.s.chapelain_at_lboro.ac.uk
Laterality in social behaviour and handedness for
spontaneous daily actions and for an experimental
task in 36 bonobos
Method
Laterality in social behaviour
19 bonobos from 2 zoos (Twycross, UK Apenheul,
Holland). 155 days of observations. direct
observation (dictaphone). ad libitum group
sampling. I observed spontaneous social
interactions. Data collected identity of the
individuals, side of approach, reaction of the
approached individual, interaction following the
approach, relative position during the interaction
Functions of Brain Lateralization Advantages
at the individual-level improves brain
efficiency allows simultaneous processing of
different processes, avoids hemispheric
competition, avoids replication of functions.
improves cognitive skills and behavioural
efficiency. Advantages of population-level
laterality social ? The direction of
asymmetries is often the same in most individuals
of a population. Based on evidences from low
vertebrates, a new theory proposes that this
population-level laterality may have been
selected under social pressures, to improve the
ability to interact with conspecifics. If most
individuals display the same laterality this may
create a certain predictability in behaviour and
facilitate social interactions. The theory
predicts that social related functions would be
lateralized and that laterality would be present
in social behaviour.
Results
Analysis in progress, we present here data from
the one month pilot study (9 bonobos, Twycross)
  • Approach before the interaction
  • - Bokela and Banya preferred to approach others
    from their left visual field, Cheka from their
    right visual field. No group-level bias to
    approach others from one visual field.
  • - Banya was approached more often from its left
    visual field. No group-level bias to be
    approached from one visual field more often.
  • - Dyad-level analysis preferences of the
    approaching individuals could depend on the
    approached individual identity. e.g. the dominant
    male specifically induced preferences in the
    approach.
  • Approached individuals reacted by accept
    more often when approached in the left visual
    field.

Support for the social related hypothesis Chicks
the hierarchy is maintained better when the
individuals are lateralized. Fishes social
species show population-level laterality,
non-social species tend to show only
individual-level laterality. Primates baboons
preferentially place themselves with the congener
on their left side. Preferences to place itself
relative to the congener would reflect a visual
field preference to monitor the congener, as
evidenced in low vertebrates.
  • During the interaction
  • - approaching individuals Bokela and Luo
    preferred to have the approached individual in
    the left visual field. Group-level bias to have
    the approached individual in the left visual
    field.
  • approached individuals Bokela was more often
    located in the left visual field of approached
    individuals. Banya had approaching individuals
    more often in its left visual field.
  • No group-level bias, but trend for the
    approaching individuals to be located more often
    in the left visual field of the approached
    individual.
  • - Approached individuals reacted by accept
    more often when the approaching individual was
    located in the left visual field.

Conclusion
Social related Hypothesis Does laterality exist
in social behaviour in bonobos ? 1. Is there a
preferred side to approach a congener ? 2. Does
the reaction of the approached subject depend on
the side of approach ? 3. Is there a side
preference to place itself relative to the
congener during dyadic interactions ? 4. Does the
interaction depend on the side of approach or
relative position during interaction ? 5. Do
lateral preferences depend on the interaction
type, relative social status, age/sex class ?
Evidences of asymmetries in the approach and the
relative position during interactions
individual and group-level biases, mostly left
sided. The presence of asymmetries in the social
behaviour, and the influence of the specific
relationship between the two individuals
involved, would support the social related
hypothesis.
Handedness in spontaneous actions (non-social and
social) and for an experimental bimanual task
Methods 36 bonobos. 3 zoos (Twycross, UK
Stuttgart, Germany Apenheul, Holland). March to
October 2006 - spontaneous actions direct
observation (dictaphone), ad libitum group
sampling. - experimental task 10 days of tests
per group. videos. focal sampling.
90 of humans are right-handed. Despite an
important database, handedness in non-human
primates is highly controversial hand
preferences are usually weak and individual (no
group-level bias). almost no data in bonobos. We
studied hand use in 36 bonobos, for 3 groups of
behaviours.
  • Results
  • Spontaneous actions analysis in progress. we
    present preliminary data from a subsample of
    subjects
  • non-social actions individual preferences for
    the behaviours reach, eat, pull grass out, cross
    arms, hang, carry object.
  • social actions strong individual preferences
    for the behaviours ventral embrace, play, drag,
    grasp, hit, touch, hold hand cradle, pick up
    and carry baby. Gestures display, invite.
  • experimental bimanual task (frequency) data for
    29 bonobos. strong individual
  • preferences (mean pref. 78). 11 right-handers,
    15 left-handers, 3 not lateralized.

- non-social actions e.g. food related. only 5
studies on hand preference in bonobos and on
small groups (N 15). Evidences of manual
preferences.
  • social actions actions occuring in the social
    context. Along with the gestural origin of
    language hypothesis, the left hemisphere may
    have controlled gestures prior to the emergence
    of speech, and may have led to a left hemisphere
    control of language.
  • A right hand preference for gesturing has been
    reported in chimpanzees, which suggests a left
    cerebral control of gestures, and would support
    the hypothesis. Few data in the bonobo, despite
    of its outstanding linguistics skills.

Conclusion Evidences of manual preferences for
several actions suggesting brain lateralization
for manual functions
  • experimental task the more complex the task is,
    the stronger the preferences are.
  • We assessed preferences with a complex task
    requiring a bimanual coordination along with a
    precise action holding a tube while reaching for
    food inside with the other hand. This tube
    task has revealed strong preferences in other
    species, and right-handedness in chimpanzees.
    Bonobos had never been tested.

Casperd JM, Dunbar, RIM. 1996. Asymmetries in the
visual processing of emotional cues during
agonistic interactions by gelada baboons.
Behavioural Processes 37 57-65. Chapelain A,
Hogervorst E, Blois-Heulin C. submitted.
Laterality in social behaviour in bonobos (Pan
paniscus) preliminary results. Chapelain A,
Hogervorst E. submitted. Hand preferences for
bimanual coordination (tube task) in 29 bonobos
(Pan paniscus). Ghirlanda S, Vallortigara G.
2004. The evolution of brain lateralization a
game-theoretical analysis of population
structure. Proceedings of the Royal Society of
London 271 853-857. Hopkins WD. 2006.
Comparative and familial analysis of handedness
in great apes. Psychological Bulletin 132
538-559. Rogers LJ, Andrew RJ. 2002. Comparative
vertebrate lateralization. Cambridge Cambridge
University Press. Vallortigara G, Rogers LJ.
2005. Survival with an asymmetrical brain
advantages and disadvantages of cerebral
lateralization. Behavioural and Brain Sciences
28 575-589. Vauclair J, 2004. Lateralization of
communicative signals in nonhuman primates and
the hypothesis of the gestural origin of
language. Interaction studies 5 365-386.
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