Abstract

Many organisms avoid habitats posing risks of parasitism. Parasites are not generally conspicuous, however, which raises the question of what cues individuals use to detect parasitism risk. Here, we provide evidence in alpine newts (Ichthyosaura alpestris) that non-visual cues from parasite-exposed conspecifics inform habitat avoidance. Alpine newts breed in aquatic habitats and occasionally move among adjacent terrestrial habitat during breeding seasons. We completed experiments with newts whereby individuals had access to both habitats, and the aquatic habitats varied in prior occupancy by conspecifics with different histories of exposure to the parasitic skin fungus, Batrachochytrium dendrobatidis (Bd). Continuous filming of newt activity for 2 days provided little evidence that prior use of aquatic habitats by conspecifics, regardless of their Bd exposure history, immediately influenced newt habitat use. However, newts that encountered aquatic habitats used specifically by Bd-exposed conspecifics on day 1 spent less time aquatic on day 2, whereas other newts did not alter habitat use. Responses could have been elicited by cues generated by Bd stages on the conspecifics or, perhaps more likely, cues emitted by the conspecifics themselves. In either case, these observations suggest that newts use non-visual cues sourced from exposed conspecifics to detect Bd risk and that those cues cause newts to avoid aquatic habitats. Bd may therefore influence host behavior in early phases of interactions, and possibly before any contact with infectious stages is made, creating potential for non-consumptive effects.

Highlights

  • Avoiding habitats containing parasites poses clear benefits

  • Neither general conspecific cues nor Batrachochytrium dendrobatidis (Bd)-exposed conspecific cues influenced any measures of newt habitat use on the first day

  • Newts tended to make fewer transitions between aquatic and terrestrial habitats on day 2 after encountering water from Bdexposed conspecifics on day 1 compared with newts that did not encounter those conditions on day 1 (Figure 1B)

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Summary

Introduction

Parasitic infections can be detrimental to individual health and fitness, and in some cases, lead to population collapses (Bosch et al, 2001; Briggs et al, 2010). Free-living organisms can minimize the likelihood of being parasitized by reducing time in habitats posing a risk of infection (Hutchings et al, 2001; Koprivnikar and Penalva, 2015; Daversa et al, 2018a; Mierzejewski et al, 2019). Parasite avoidance can affect higher-order ecological processes, exemplified by trophic cascades that restructure entire ecosystems (Buck and Ripple, 2017; Buck et al, 2018). Infective parasite stages are in most cases too small relative to their hosts to visually detect, which raises the question of what cues hosts use to avoid habitats posing a risk of infection

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