Testing the habituation assumption underlying models of parasitoid foraging behavior
- Published
- Accepted
- Subject Areas
- Animal Behavior, Ecology, Entomology
- Keywords
- learning, optimal foraging theory, habituation, patch exploitation, infochemical cues
- Copyright
- © 2016 Abram et al.
- Licence
- This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ Preprints) and either DOI or URL of the article must be cited.
- Cite this article
- 2016. Testing the habituation assumption underlying models of parasitoid foraging behavior. PeerJ Preprints 4:e2555v1 https://doi.org/10.7287/peerj.preprints.2555v1
Abstract
Habituation, a form of non-associative learning, has several well-defined characteristics that apply to a wide range of physiological and behavioral responses in many organisms. In classic patch time allocation models, habituation is considered to be a major mechanistic component of parasitoid behavioral strategies. However, parasitoid behavioral responses to host cues have not previously been tested for the known, specific characteristics of habituation. Here, we tested whether the foraging behavior of the egg parasitoid Trissolcus basalis shows specific characteristics of habituation in response to consecutive encounters with patches of host (Nezara viridula) chemical contact cues (footprints), in particular: (i) a training interval-dependent decline in response intensity, and (ii) a training interval dependent recovery of the response. As would be expected of a habituated response, wasps trained at higher frequencies decreased their behavioral response to host footprints more quickly and to a greater degree than those trained at low frequencies, and subsequently showed a more rapid, although partial, recovery of their behavioral response to host footprints. In contrast to previously studied forms of parasitoid memory (i.e., from associative learning), this putative habituation learning could not be blocked by cold anesthesia, ingestion of an ATPase inhibitor, or ingestion of a protein synthesis inhibitor. Our study provides support for the assumption that diminishing responses of parasitoids to chemical indicators of host presence constitutes habituation as opposed to sensory fatigue, and may indicate that the underlying mechanisms differ from other, better-studied forms of parasitoid learning.
Author Comment
This is a submission to PeerJ for review.