Aggressive behaviour within pairs of male crickets leads to the establishment of a dominance hierarchy. Defeated males avoid their victorious adversaries for several hours before regaining aggressiveness. However, the defeated male does not regain aggressiveness if repeated fighting occurs. Loss of individual aggressiveness is limited by group size, which constrains the number of crickets fighting at any given time. Thus, group aggressive behaviour is modulated by an environmental factor, group size, which is ultimately determined by individual actions, i.e. fighting between two individuals. We developed a robot model to elucidate the mechanism of group-size-dependent behaviour alternation in crickets. The behaviour of individual robots was evaluated experimentally with mobile robots and the group behaviour of the robots was evaluated by computer simulation. We demonstrated that the group-size-dependent strategy in crickets could be generated by local interactions between robots, where the behaviour was governed by an oscillator and memory of the outcome of previous fights.
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Ecol Lett
March 2020
Graduate School of Accounting and Department of Applied Mathematics, Waseda University, Nishi-waseda 1-6-1, Shinjuku, Tokyo, 169-8050, Japan.
The origin of eusociality in the Hymenoptera is a question of major interest. Theory has tended to focus on genetic relatedness, but ecology can be just as important a determinant of whether eusociality evolves. Using the model of Fu et al.
View Article and Find Full Text PDFPhys Rev E
March 2019
Centre for Ecological Sciences, Indian Institute of Science, Bengaluru, 560 012, India.
Many animal groups are heterogeneous and may even consist of individuals of different species, called mixed-species flocks. Mathematical and computational models of collective animal movement behavior, however, typically assume that groups and populations consist of identical individuals. In this paper, using the mathematical framework of the coagulation-fragmentation process, we develop and analyze a model of merge and split group dynamics, also called fission-fusion dynamics, for heterogeneous populations that contain two types (or species) of individuals.
View Article and Find Full Text PDFProc Biol Sci
November 2015
Centre for Ecology and Conservation, College of Life and Environmental Sciences, University of Exeter, Penryn Campus, Cornwall TR10 9FE, UK
Life-history theory assumes that reproduction entails a cost, and research on cooperatively breeding societies suggests that the cooperative sharing of workloads can reduce this cost. However, the physiological mechanisms that underpin both the costs of reproduction and the benefits of cooperation remain poorly understood. It has been hypothesized that reproductive costs may arise in part from oxidative stress, as reproductive investment may elevate exposure to reactive oxygen species, compromising survival and future reproduction and accelerating senescence.
View Article and Find Full Text PDFProc Biol Sci
August 2014
Behavioural Ecology, Institute of Ecology and Evolution, University of Bern, Wohlenstrasse 50a, 3032 Hinterkappelen, Switzerland.
In cooperative breeding systems, dominant breeders sometimes tolerate unrelated individuals even if they inflict costs on the dominants. According to the 'pay-to-stay' hypothesis, (i) subordinates can outweigh these costs by providing help and (ii) dominants should be able to enforce help by punishing subordinates that provide insufficient help. This requires that dominants can monitor helping and can recognize group members individually.
View Article and Find Full Text PDFBiophys J
September 2013
Department of Physiology, McGill University, Montréal, Québec, Canada; Centre for Applied Mathematics in Bioscience and Medicine, McGill University, Montréal, Québec, Canada; Meakins-Christie Laboratories, McGill University, Montréal, Québec, Canada.
Naturally occurring groups of muscle myosin behave differently from individual myosins or small groups commonly assayed in vitro. Here, we investigate the emergence of myosin group behavior with increasing myosin group size. Assuming the number of myosin binding sites (N) is proportional to actin length (L) (N = L/35.
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