Abstract

Animals often show high consistency in their social organisation despite facing changing environmental conditions. Especially in shoaling fish, fission–fusion dynamics that describe for which periods individuals are solitary or social have been found to remain unaltered even when density changed. This compensatory ability is assumed to be an adaptation towards constant predation pressure, but the mechanism through which individuals can actively compensate for density changes is yet unknown. The aim of the current study is to identify behavioural patterns that enable this active compensation. We compared the fission–fusion dynamics of two populations of the live-bearing Atlantic molly (Poecilia mexicana) that live in adjacent habitats with very different predator regimes: cave mollies that inhabit a low-predation environment inside a sulfidic cave with a low density of predatory water bugs (Belostoma sp.), and mollies that live directly outside the cave (henceforth called “surface” mollies) in a high-predation environment. We analysed their fission–fusion dynamics under two different fish densities of 12 and 6 fish per 0.36 m2. As expected, surface mollies spent more time being social than cave mollies, and this difference in social time was a result of surface mollies being less likely to discontinue social contact (once they had a social partner) and being more likely to resume social contact (once alone) than cave mollies. Interestingly, surface mollies were also less likely to switch among social partners than cave mollies. A random walk simulation predicted each population to show reduced social encounters in the low density treatment. While cave mollies largely followed this prediction, surface mollies maintained their interaction probabilities even at low density. Surface mollies achieved this by a reduction in the size of a convex polygon formed by the group as density decreased. This may allow them to largely maintain their fission–fusion dynamics while still being able to visit large parts of the available area as a group. A slight reduction (21%) in the area visited at low densities was also observed but insufficient to explain how the fish maintained their fission–fusion dynamics. Finally, we discuss potential movement rules that could account for the reduction of polygon size and test their performance.

Highlights

  • In many group-living animals, individuals switch frequently between social and solitary periods (Krause & Ruxton, 2002)

  • We explored three different behavioural aspects that can be responsible for the assumed density compensation of fission–fusion dynamics: (a) fish might swim at higher speeds, (b) fish might reduce the area usage to a particular part of the experimental arena, and (c) the polygon formed by the group might decrease while allowing fish to explore most of the arena

  • Surface mollies showed a higher probability to join a new social partner once they were alone compared to cave mollies

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Summary

Introduction

In many group-living animals, individuals switch frequently between social and solitary periods (Krause & Ruxton, 2002) This type of social interaction is wide-spread and known as fission–fusion dynamics (Aureli et al, 2008; Couzin & Laidre, 2009). Anybody who has ever observed fish will have noticed the extremely frequent fission–fusion dynamics at the rate of a few seconds that many species display. The duration of these associations between individuals follows a geometric distribution (i.e., with short associations being very frequent and long ones very rare, see Wilson et al, 2015b; Wilson et al, 2015a). The underlying idea is that the maintenance of geometric fission–fusion dynamics combines the benefits of group-living (e.g., to lower an individual’s risk of predation) with those of being solitary (e.g., lower resource competition) without becoming predictable to predators

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