Publications

Abstract

Animal acoustic communication contains many structural features. Among these, temporal structure, or rhythmicity, is increasingly tested empirically and modelled quantitatively. Accelerando is a rhythmic structure which consists of temporal intervals increasing in rate over a sequence. Why this particular vocal behaviour is widespread in many different animal lineages, and how it evolved, is so far unknown. Here, we use evolutionary game theory and computer simulations to link two rhythmic aspects of animal communication, acceleration and overlap: We test whether rhythmic accelerando could evolve under a pressure for acoustic overlap in time. Our models show that higher acceleration values result in a higher payoff, driven by the higher relative overlap between sequences. The addition of a cost to the payoff matrix models a physiological disadvantage to high acceleration rates and introduces a divergence between an individual’s incentive and the overall payoff of the population. Analysis of the invasion dynamics of acceleration strategies shows a stable, non-invadable range of strategies for moderate acceleration levels. Our computational simulations confirm these results: A simple selective pressure to maximise the expected overlap, while minimising the associated physiological cost, causes an initially isochronous population to evolve towards producing increasingly accelerating sequences until a population-wide equilibrium of rhythmic accelerando is reached. These results are robust to a broad range of parameter values. Overall, our analyses show that if overlap is beneficial, emergent evolutionary dynamics allow a population to gradually start producing accelerating sequences and reach a stable state of moderate acceleration. Finally, our modelling results closely match empirical data recorded from an avian species showing rhythmic accelerando, the African penguin. This shows the productive interplay between theoretical and empirical biology.

Abstract

To study patterns in behavior, fitness, and population dynamics, estimating the age of the individuals is often a necessity. Specifically, age estimation of young animals is very important for animal rehabilitation centers because it may determine if the animal should be taken in and, if so, what care is optimal for its rehabilitation. Accurate age estimation is also important to determine the growth pattern of an individual, and it is needed to correctly interpret the influence of early body condition on its growth trajectories. The purpose of our study was to find body measurements that function as good age estimators in young (up to 3 months old) harbor seals (Phoca vitulina vitulina), placing emphasis on noninvasive techniques that can be used in the field. To meet this goal, body mass (BM), dorsal standard length (DSL), upper canine length (CL), body condition (BC), and sex were determined from 45 Harbor Seal pups of known age. Generalized additive mixed models were fitted to find how well these morphometric measures predicted age, and the results from the selected model were used to compute growth curves and to create a practical table to determine the age of young animals in the field. We found that both DSL and CL—and to some extent sex—were useful predictors for estimating age in young harbor seals and that the growth rate of pups raised in captivity is significantly lower than for those raised in the wild. In addition, we found no evidence for compensatory growth, given that animals that arrived at the center with a poor BM or BC continued to show lower BM or BC throughout almost the entire rehabilitation period.

Abstract

Time is one crucial dimension conveying information in animal communication. Evolution has shaped animals’ nervous systems to produce signals with temporal properties fitting their socio-ecological niches. Many quantitative models of mechanisms underlying rhythmic behaviour exist, spanning insects, crustaceans, birds, amphibians, and mammals. However, these computational and mathematical models are often presented in isolation. Here, we provide an overview of the main mathematical models employed in the study of animal rhythmic communication among conspecifics. After presenting basic definitions and mathematical formalisms, we discuss each individual model. These computational models are then compared using simulated data to uncover similarities and key differences in the underlying mechanisms found across species. Our review of the empirical literature is admittedly limited. We stress the need of using comparative computer simulations – both before and after animal experiments – to better understand animal timing in interaction. We hope this article will serve as a potential first step towards a common computational framework to describe temporal interactions in animals, including humans.

Abstract

The study of human language is progressively moving toward comparative and interactive frameworks, extending the concept of turn‐taking to animal communication. While such an endeavor will help us understand the interactive origins of language, any theoretical account for cross‐species turn‐taking should consider three key points. First, animal turn‐taking must incorporate biological studies on animal chorusing, namely how different species coordinate their signals over time. Second, while concepts employed in human communication and turn‐taking, such as intentionality, are still debated in animal behavior, lower level mechanisms with clear neurobiological bases can explain much of animal interactive behavior. Third, social behavior, interactivity, and cooperation can be orthogonal, and the alternation of animal signals need not be cooperative. Considering turn‐taking a subset of chorusing in the rhythmic dimension may avoid overinterpretation and enhance the comparability of future empirical work.