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Adapted to Roar: Functional Morphology of Tiger and Lion Vocal Folds

Vocal production requires active control of the respiratory system, larynx and vocal tract. Vocal sounds in mammals are produced by flow-induced vocal fold oscillation, which requires vocal fold tissue that can sustain the mechanical stress during phonation. Our understanding of the relationship bet...

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Autores principales: Klemuk, Sarah A., Riede, Tobias, Walsh, Edward J., Titze, Ingo R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206895/
https://www.ncbi.nlm.nih.gov/pubmed/22073246
http://dx.doi.org/10.1371/journal.pone.0027029
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author Klemuk, Sarah A.
Riede, Tobias
Walsh, Edward J.
Titze, Ingo R.
author_facet Klemuk, Sarah A.
Riede, Tobias
Walsh, Edward J.
Titze, Ingo R.
author_sort Klemuk, Sarah A.
collection PubMed
description Vocal production requires active control of the respiratory system, larynx and vocal tract. Vocal sounds in mammals are produced by flow-induced vocal fold oscillation, which requires vocal fold tissue that can sustain the mechanical stress during phonation. Our understanding of the relationship between morphology and vocal function of vocal folds is very limited. Here we tested the hypothesis that vocal fold morphology and viscoelastic properties allow a prediction of fundamental frequency range of sounds that can be produced, and minimal lung pressure necessary to initiate phonation. We tested the hypothesis in lions and tigers who are well-known for producing low frequency and very loud roaring sounds that expose vocal folds to large stresses. In histological sections, we found that the Panthera vocal fold lamina propria consists of a lateral region with adipocytes embedded in a network of collagen and elastin fibers and hyaluronan. There is also a medial region that contains only fibrous proteins and hyaluronan but no fat cells. Young's moduli range between 10 and 2000 kPa for strains up to 60%. Shear moduli ranged between 0.1 and 2 kPa and differed between layers. Biomechanical and morphological data were used to make predictions of fundamental frequency and subglottal pressure ranges. Such predictions agreed well with measurements from natural phonation and phonation of excised larynges, respectively. We assume that fat shapes Panthera vocal folds into an advantageous geometry for phonation and it protects vocal folds. Its primary function is probably not to increase vocal fold mass as suggested previously. The large square-shaped Panthera vocal fold eases phonation onset and thereby extends the dynamic range of the voice.
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spelling pubmed-32068952011-11-09 Adapted to Roar: Functional Morphology of Tiger and Lion Vocal Folds Klemuk, Sarah A. Riede, Tobias Walsh, Edward J. Titze, Ingo R. PLoS One Research Article Vocal production requires active control of the respiratory system, larynx and vocal tract. Vocal sounds in mammals are produced by flow-induced vocal fold oscillation, which requires vocal fold tissue that can sustain the mechanical stress during phonation. Our understanding of the relationship between morphology and vocal function of vocal folds is very limited. Here we tested the hypothesis that vocal fold morphology and viscoelastic properties allow a prediction of fundamental frequency range of sounds that can be produced, and minimal lung pressure necessary to initiate phonation. We tested the hypothesis in lions and tigers who are well-known for producing low frequency and very loud roaring sounds that expose vocal folds to large stresses. In histological sections, we found that the Panthera vocal fold lamina propria consists of a lateral region with adipocytes embedded in a network of collagen and elastin fibers and hyaluronan. There is also a medial region that contains only fibrous proteins and hyaluronan but no fat cells. Young's moduli range between 10 and 2000 kPa for strains up to 60%. Shear moduli ranged between 0.1 and 2 kPa and differed between layers. Biomechanical and morphological data were used to make predictions of fundamental frequency and subglottal pressure ranges. Such predictions agreed well with measurements from natural phonation and phonation of excised larynges, respectively. We assume that fat shapes Panthera vocal folds into an advantageous geometry for phonation and it protects vocal folds. Its primary function is probably not to increase vocal fold mass as suggested previously. The large square-shaped Panthera vocal fold eases phonation onset and thereby extends the dynamic range of the voice. Public Library of Science 2011-11-02 /pmc/articles/PMC3206895/ /pubmed/22073246 http://dx.doi.org/10.1371/journal.pone.0027029 Text en Klemuk et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Klemuk, Sarah A.
Riede, Tobias
Walsh, Edward J.
Titze, Ingo R.
Adapted to Roar: Functional Morphology of Tiger and Lion Vocal Folds
title Adapted to Roar: Functional Morphology of Tiger and Lion Vocal Folds
title_full Adapted to Roar: Functional Morphology of Tiger and Lion Vocal Folds
title_fullStr Adapted to Roar: Functional Morphology of Tiger and Lion Vocal Folds
title_full_unstemmed Adapted to Roar: Functional Morphology of Tiger and Lion Vocal Folds
title_short Adapted to Roar: Functional Morphology of Tiger and Lion Vocal Folds
title_sort adapted to roar: functional morphology of tiger and lion vocal folds
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206895/
https://www.ncbi.nlm.nih.gov/pubmed/22073246
http://dx.doi.org/10.1371/journal.pone.0027029
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