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Hosts of avian brood parasites have evolved egg signatures with elevated information content
Hosts of brood-parasitic birds must distinguish their own eggs from parasitic mimics, or pay the cost of mistakenly raising a foreign chick. Egg discrimination is easier when different host females of the same species each lay visually distinctive eggs (egg ‘signatures’), which helps to foil mimicry...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590476/ https://www.ncbi.nlm.nih.gov/pubmed/26085586 http://dx.doi.org/10.1098/rspb.2015.0598 |
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author | Caves, Eleanor M. Stevens, Martin Iversen, Edwin S. Spottiswoode, Claire N. |
author_facet | Caves, Eleanor M. Stevens, Martin Iversen, Edwin S. Spottiswoode, Claire N. |
author_sort | Caves, Eleanor M. |
collection | PubMed |
description | Hosts of brood-parasitic birds must distinguish their own eggs from parasitic mimics, or pay the cost of mistakenly raising a foreign chick. Egg discrimination is easier when different host females of the same species each lay visually distinctive eggs (egg ‘signatures’), which helps to foil mimicry by parasites. Here, we ask whether brood parasitism is associated with lower levels of correlation between different egg traits in hosts, making individual host signatures more distinctive and informative. We used entropy as an index of the potential information content encoded by nine aspects of colour, pattern and luminance of eggs of different species in two African bird families (Cisticolidae parasitized by cuckoo finches Anomalospiza imberbis, and Ploceidae by diederik cuckoos Chrysococcyx caprius). Parasitized species showed consistently higher entropy in egg traits than did related, unparasitized species. Decomposing entropy into two variation components revealed that this was mainly driven by parasitized species having lower levels of correlation between different egg traits, rather than higher overall levels of variation in each individual egg trait. This suggests that irrespective of the constraints that might operate on individual egg traits, hosts can further improve their defensive ‘signatures' by arranging suites of egg traits into unpredictable combinations. |
format | Online Article Text |
id | pubmed-4590476 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-45904762015-10-13 Hosts of avian brood parasites have evolved egg signatures with elevated information content Caves, Eleanor M. Stevens, Martin Iversen, Edwin S. Spottiswoode, Claire N. Proc Biol Sci Research Articles Hosts of brood-parasitic birds must distinguish their own eggs from parasitic mimics, or pay the cost of mistakenly raising a foreign chick. Egg discrimination is easier when different host females of the same species each lay visually distinctive eggs (egg ‘signatures’), which helps to foil mimicry by parasites. Here, we ask whether brood parasitism is associated with lower levels of correlation between different egg traits in hosts, making individual host signatures more distinctive and informative. We used entropy as an index of the potential information content encoded by nine aspects of colour, pattern and luminance of eggs of different species in two African bird families (Cisticolidae parasitized by cuckoo finches Anomalospiza imberbis, and Ploceidae by diederik cuckoos Chrysococcyx caprius). Parasitized species showed consistently higher entropy in egg traits than did related, unparasitized species. Decomposing entropy into two variation components revealed that this was mainly driven by parasitized species having lower levels of correlation between different egg traits, rather than higher overall levels of variation in each individual egg trait. This suggests that irrespective of the constraints that might operate on individual egg traits, hosts can further improve their defensive ‘signatures' by arranging suites of egg traits into unpredictable combinations. The Royal Society 2015-07-07 /pmc/articles/PMC4590476/ /pubmed/26085586 http://dx.doi.org/10.1098/rspb.2015.0598 Text en http://creativecommons.org/licenses/by/4.0/ © 2015 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Articles Caves, Eleanor M. Stevens, Martin Iversen, Edwin S. Spottiswoode, Claire N. Hosts of avian brood parasites have evolved egg signatures with elevated information content |
title | Hosts of avian brood parasites have evolved egg signatures with elevated information content |
title_full | Hosts of avian brood parasites have evolved egg signatures with elevated information content |
title_fullStr | Hosts of avian brood parasites have evolved egg signatures with elevated information content |
title_full_unstemmed | Hosts of avian brood parasites have evolved egg signatures with elevated information content |
title_short | Hosts of avian brood parasites have evolved egg signatures with elevated information content |
title_sort | hosts of avian brood parasites have evolved egg signatures with elevated information content |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590476/ https://www.ncbi.nlm.nih.gov/pubmed/26085586 http://dx.doi.org/10.1098/rspb.2015.0598 |
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