Contrasting Patterns of Sensory Adaptation in Living and Extinct Flightless Birds

Avian cranial anatomy is constrained by the competing (or complementary) requirements and costs of various facial, muscular, sensory, and central neural structures. However, these constraints may operate differently in flighted versus flightless birds. We investigated cranial sense organ morphology...

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Autores principales: Peter Johnston, Kieren J. Mitchell
Formato: article
Lenguaje:EN
Publicado: MDPI AG 2021
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moa
Acceso en línea:https://doaj.org/article/656eea544acd4ee6868fef48e9dabfb8
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spelling oai:doaj.org-article:656eea544acd4ee6868fef48e9dabfb82021-11-25T17:22:29ZContrasting Patterns of Sensory Adaptation in Living and Extinct Flightless Birds10.3390/d131105381424-2818https://doaj.org/article/656eea544acd4ee6868fef48e9dabfb82021-10-01T00:00:00Zhttps://www.mdpi.com/1424-2818/13/11/538https://doaj.org/toc/1424-2818Avian cranial anatomy is constrained by the competing (or complementary) requirements and costs of various facial, muscular, sensory, and central neural structures. However, these constraints may operate differently in flighted versus flightless birds. We investigated cranial sense organ morphology in four lineages of flightless birds: kiwi (<i>Apteryx</i>), the Kakapo (<i>Strigops habroptilus</i>), and the extinct moa (Dinornithiformes) from New Zealand; and the extinct elephant birds from Madagascar (Aepyornithidae). Scleral ring and eye measurements suggest that the Upland Moa (<i>Megalapteryx didinus</i>) was diurnal, while measurements for the Kakapo are consistent with nocturnality. Kiwi are olfactory specialists, though here we postulate that retronasal olfaction is the dominant olfactory route in this lineage. We suggest that the Upland Moa and aepyornithids were also olfactory specialists; the former additionally displaying prominent bill tip sensory organs implicated in mechanoreception. Finally, the relative size of the endosseous cochlear duct revealed that the Upland Moa had a well-developed hearing sensitivity range, while the sensitivity of the kiwi, Kakapo, and aepyornithids was diminished. Together, our results reveal contrasting sensory strategies among extant and extinct flightless birds. More detailed characterisation of sensory capacities and cranial anatomy in extant birds may refine our ability to make accurate inferences about the sensory capacities of fossil taxa.Peter JohnstonKieren J. MitchellMDPI AGarticlemoa<i>Aepyornis</i>kiwikakapoolfactionvisionBiology (General)QH301-705.5ENDiversity, Vol 13, Iss 538, p 538 (2021)
institution DOAJ
collection DOAJ
language EN
topic moa
<i>Aepyornis</i>
kiwi
kakapo
olfaction
vision
Biology (General)
QH301-705.5
spellingShingle moa
<i>Aepyornis</i>
kiwi
kakapo
olfaction
vision
Biology (General)
QH301-705.5
Peter Johnston
Kieren J. Mitchell
Contrasting Patterns of Sensory Adaptation in Living and Extinct Flightless Birds
description Avian cranial anatomy is constrained by the competing (or complementary) requirements and costs of various facial, muscular, sensory, and central neural structures. However, these constraints may operate differently in flighted versus flightless birds. We investigated cranial sense organ morphology in four lineages of flightless birds: kiwi (<i>Apteryx</i>), the Kakapo (<i>Strigops habroptilus</i>), and the extinct moa (Dinornithiformes) from New Zealand; and the extinct elephant birds from Madagascar (Aepyornithidae). Scleral ring and eye measurements suggest that the Upland Moa (<i>Megalapteryx didinus</i>) was diurnal, while measurements for the Kakapo are consistent with nocturnality. Kiwi are olfactory specialists, though here we postulate that retronasal olfaction is the dominant olfactory route in this lineage. We suggest that the Upland Moa and aepyornithids were also olfactory specialists; the former additionally displaying prominent bill tip sensory organs implicated in mechanoreception. Finally, the relative size of the endosseous cochlear duct revealed that the Upland Moa had a well-developed hearing sensitivity range, while the sensitivity of the kiwi, Kakapo, and aepyornithids was diminished. Together, our results reveal contrasting sensory strategies among extant and extinct flightless birds. More detailed characterisation of sensory capacities and cranial anatomy in extant birds may refine our ability to make accurate inferences about the sensory capacities of fossil taxa.
format article
author Peter Johnston
Kieren J. Mitchell
author_facet Peter Johnston
Kieren J. Mitchell
author_sort Peter Johnston
title Contrasting Patterns of Sensory Adaptation in Living and Extinct Flightless Birds
title_short Contrasting Patterns of Sensory Adaptation in Living and Extinct Flightless Birds
title_full Contrasting Patterns of Sensory Adaptation in Living and Extinct Flightless Birds
title_fullStr Contrasting Patterns of Sensory Adaptation in Living and Extinct Flightless Birds
title_full_unstemmed Contrasting Patterns of Sensory Adaptation in Living and Extinct Flightless Birds
title_sort contrasting patterns of sensory adaptation in living and extinct flightless birds
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/656eea544acd4ee6868fef48e9dabfb8
work_keys_str_mv AT peterjohnston contrastingpatternsofsensoryadaptationinlivingandextinctflightlessbirds
AT kierenjmitchell contrastingpatternsofsensoryadaptationinlivingandextinctflightlessbirds
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