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The evolution of anti-bat sensory illusions in moths
Prey transmit sensory illusions to redirect predatory strikes, creating a discrepancy between what a predator perceives and reality. We use the acoustic arms race between bats and moths to investigate the evolution and function of a sensory illusion. The spinning hindwing tails of silk moths (Saturn...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031379/ https://www.ncbi.nlm.nih.gov/pubmed/29978042 http://dx.doi.org/10.1126/sciadv.aar7428 |
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author | Rubin, Juliette J. Hamilton, Chris A. McClure, Chris J. W. Chadwell, Brad A. Kawahara, Akito Y. Barber, Jesse R. |
author_facet | Rubin, Juliette J. Hamilton, Chris A. McClure, Chris J. W. Chadwell, Brad A. Kawahara, Akito Y. Barber, Jesse R. |
author_sort | Rubin, Juliette J. |
collection | PubMed |
description | Prey transmit sensory illusions to redirect predatory strikes, creating a discrepancy between what a predator perceives and reality. We use the acoustic arms race between bats and moths to investigate the evolution and function of a sensory illusion. The spinning hindwing tails of silk moths (Saturniidae) divert bat attack by reflecting sonar to create a misleading echoic target. We characterized geometric morphometrics of moth hindwings across silk moths, mapped these traits onto a new, robust phylogeny, and found that elaborated hindwing structures have converged on four adaptive shape peaks. To test the mechanism underlying these anti-bat traits, we pit bats against three species of silk moths with experimentally altered hindwings that created a representative gradient of ancestral and extant hindwing shapes. High-speed videography of battles reveals that moths with longer hindwings and tails more successfully divert bat attack. We postulate that sensory illusions are widespread and are underappreciated drivers of diversity across systems. |
format | Online Article Text |
id | pubmed-6031379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-60313792018-07-05 The evolution of anti-bat sensory illusions in moths Rubin, Juliette J. Hamilton, Chris A. McClure, Chris J. W. Chadwell, Brad A. Kawahara, Akito Y. Barber, Jesse R. Sci Adv Research Articles Prey transmit sensory illusions to redirect predatory strikes, creating a discrepancy between what a predator perceives and reality. We use the acoustic arms race between bats and moths to investigate the evolution and function of a sensory illusion. The spinning hindwing tails of silk moths (Saturniidae) divert bat attack by reflecting sonar to create a misleading echoic target. We characterized geometric morphometrics of moth hindwings across silk moths, mapped these traits onto a new, robust phylogeny, and found that elaborated hindwing structures have converged on four adaptive shape peaks. To test the mechanism underlying these anti-bat traits, we pit bats against three species of silk moths with experimentally altered hindwings that created a representative gradient of ancestral and extant hindwing shapes. High-speed videography of battles reveals that moths with longer hindwings and tails more successfully divert bat attack. We postulate that sensory illusions are widespread and are underappreciated drivers of diversity across systems. American Association for the Advancement of Science 2018-07-04 /pmc/articles/PMC6031379/ /pubmed/29978042 http://dx.doi.org/10.1126/sciadv.aar7428 Text en Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Rubin, Juliette J. Hamilton, Chris A. McClure, Chris J. W. Chadwell, Brad A. Kawahara, Akito Y. Barber, Jesse R. The evolution of anti-bat sensory illusions in moths |
title | The evolution of anti-bat sensory illusions in moths |
title_full | The evolution of anti-bat sensory illusions in moths |
title_fullStr | The evolution of anti-bat sensory illusions in moths |
title_full_unstemmed | The evolution of anti-bat sensory illusions in moths |
title_short | The evolution of anti-bat sensory illusions in moths |
title_sort | evolution of anti-bat sensory illusions in moths |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031379/ https://www.ncbi.nlm.nih.gov/pubmed/29978042 http://dx.doi.org/10.1126/sciadv.aar7428 |
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