First published online July 25, 2005
Journal of Experimental Biology 208, 2903-2912 (2005)
Published by The Company of Biologists 2005
doi: 10.1242/jeb.01711
Temporal organization of bi-directional traffic in the ant Lasius niger (L.)
Audrey Dussutour1,*,
Jean-Louis Deneubourg2 and
Vincent Fourcassié1,
1 Centre de Recherches sur la Cognition Animale, UMR CNRS 5169,
Université Paul Sabatier, 118 route de Narbonne, F-31062, Toulouse
Cedex 4, France
2 Service d'Ecologie Sociale and Centre d'Etudes des
Phénomènes Non-linéaires et des Systèmes
Complexes, Université Libre de Bruxelles, CP231, Boulevard du Triomphe,
B-1050 Bruxelles, Belgium

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Fig. 1. Schematic illustration of the 3 mm-width bridge, with the different sectors
defined for the analysis of the ants' individual behaviour.
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Fig. 2. Mean number of ants per minute crossing the bridge in both directions every
3 min. Values are means ± S.E.M.
N=15 trials for both bridge widths.
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Fig. 3. Effect of the number of encounters with contact on the duration of travel
between the two bottlenecks of the bridge for the two bridge widths studied.
The slope of the linear regression lines corresponds to the time lost by each
ant per interaction; its intercept gives the duration of travel without
interaction. N=133 and N=126 for the 3 mm and 10 mm bridge,
respectively.
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Fig. 4. Relationship between the number of encounters with contact and the total
number of encounters per ant for each bridge width studied. The slope of the
lines corresponds to the probability of an ant travelling on the bridge to be
contacted by another ant during an encounter. N=133 and
N=126 for the 3 mm and 10 mm bridge, respectively.
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Fig. 5. Experimental results. Distribution frequency of the size of the groups of
successive ants travelling in the same direction identified at the level of
the line between the bottleneck and the entrance on the nest side of the
bridge for each bridge width. The distribution frequency of group size
obtained with a random sequence of ants generated on the basis of an equal
probability of occurrence of nestbound and outbound ants is also represented.
N=1203 and N=905 for the 10 mm and 3 mm bridge,
respectively.
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Fig. 6. Distribution of the time spent crossing the bottlenecks and the entrances
for ants travelling to and from the centre of a 3 mm bridge (for each sector,
the results for the nest and source sides of the bridge have been pooled). The
dotted lines within the boxplots represent the median, the lower and upper
boundaries of the boxes represent, respectively, the 25th and 75th
percentiles, while the whiskers extend to the smallest and largest values
within 1.5 box lengths. The open circles represent the outliers.
N=500 for each box plot.
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Fig. 7. Simulation results. Distribution frequency of the size of the groups of
successive ants travelling in the same direction at the level of the line
between the bottleneck and the entrance on the nest side of the bridge when
the simulations were run with a flow of ants entering the bottlenecks of the
bridge equal to 0.5 ants per time step, corresponding to the flow measured in
the experiments on a 3 mm bridge. The simulations were run with and without
implementing a cooperative rule between following ants. For explanations on
the random distribution, see Fig.
5.
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Fig. 8. Simulation results. Distribution frequency of the size of groups of
successive ants travelling in the same direction at the level of the line
between the bottleneck and the entrance on the nest side of the bridge, when
the simulations were run with increasing values of the flow of ants entering
the bridge. For explanations on the random distribution, see
Fig. 5. The inset shows the
mean group size obtained for different values of entrance flow.
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© The Company of Biologists Ltd 2005