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Hidden diversity: comparative functional morphology of humans and other species

Gastrointestinal (GI) morphology plays an important role in nutrition, health, and epidemiology; yet limited data on GI variation have been collected since 1885. Here we demonstrate that students can collect reliable data sets on gut morphology; when they do, they reveal greater morphological variat...

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Autores principales: McKenney, Erin A., Hale, Amanda R., Anderson, Janiaya, Larsen, Roxanne, Grant, Colleen, Dunn, Robert R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10135406/
https://www.ncbi.nlm.nih.gov/pubmed/37123005
http://dx.doi.org/10.7717/peerj.15148
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author McKenney, Erin A.
Hale, Amanda R.
Anderson, Janiaya
Larsen, Roxanne
Grant, Colleen
Dunn, Robert R.
author_facet McKenney, Erin A.
Hale, Amanda R.
Anderson, Janiaya
Larsen, Roxanne
Grant, Colleen
Dunn, Robert R.
author_sort McKenney, Erin A.
collection PubMed
description Gastrointestinal (GI) morphology plays an important role in nutrition, health, and epidemiology; yet limited data on GI variation have been collected since 1885. Here we demonstrate that students can collect reliable data sets on gut morphology; when they do, they reveal greater morphological variation for some structures in the GI tract than has been documented in the published literature. We discuss trait variability both within and among species, and the implications of that variability for evolution and epidemiology. Our results show that morphological variation in the GI tract is associated with each organ’s role in food processing. For example, the length of many structures was found to vary significantly with feeding strategy. Within species, the variability illustrated by the coefficients of variation suggests that selective constraints may vary with function. Within humans, we detected significant Pearson correlations between the volume of the liver and the length of the appendix (t-value = 2.5278, df = 28, p = 0.0174, corr = 0.4311) and colon (t-value = 2.0991, df = 19, p = 0.0494, corr = 0.4339), as well as between the lengths of the small intestine and colon (t-value = 2.1699, df = 17, p = 0.0445, corr = 0.4657), which are arguably the most vital organs in the gut for nutrient absorption. Notably, intraspecific variation in the small intestine can be associated with life history traits. In humans, females demonstrated consistently and significantly longer small intestines than males (t-value(15) = 2.245, p = 0.0403). This finding supports the female canalization hypothesis, specifically, increased female investment in the digestion and absorption of lipids.
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spelling pubmed-101354062023-04-28 Hidden diversity: comparative functional morphology of humans and other species McKenney, Erin A. Hale, Amanda R. Anderson, Janiaya Larsen, Roxanne Grant, Colleen Dunn, Robert R. PeerJ Anthropology Gastrointestinal (GI) morphology plays an important role in nutrition, health, and epidemiology; yet limited data on GI variation have been collected since 1885. Here we demonstrate that students can collect reliable data sets on gut morphology; when they do, they reveal greater morphological variation for some structures in the GI tract than has been documented in the published literature. We discuss trait variability both within and among species, and the implications of that variability for evolution and epidemiology. Our results show that morphological variation in the GI tract is associated with each organ’s role in food processing. For example, the length of many structures was found to vary significantly with feeding strategy. Within species, the variability illustrated by the coefficients of variation suggests that selective constraints may vary with function. Within humans, we detected significant Pearson correlations between the volume of the liver and the length of the appendix (t-value = 2.5278, df = 28, p = 0.0174, corr = 0.4311) and colon (t-value = 2.0991, df = 19, p = 0.0494, corr = 0.4339), as well as between the lengths of the small intestine and colon (t-value = 2.1699, df = 17, p = 0.0445, corr = 0.4657), which are arguably the most vital organs in the gut for nutrient absorption. Notably, intraspecific variation in the small intestine can be associated with life history traits. In humans, females demonstrated consistently and significantly longer small intestines than males (t-value(15) = 2.245, p = 0.0403). This finding supports the female canalization hypothesis, specifically, increased female investment in the digestion and absorption of lipids. PeerJ Inc. 2023-04-24 /pmc/articles/PMC10135406/ /pubmed/37123005 http://dx.doi.org/10.7717/peerj.15148 Text en ©2023 McKenney et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , 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) and either DOI or URL of the article must be cited.
spellingShingle Anthropology
McKenney, Erin A.
Hale, Amanda R.
Anderson, Janiaya
Larsen, Roxanne
Grant, Colleen
Dunn, Robert R.
Hidden diversity: comparative functional morphology of humans and other species
title Hidden diversity: comparative functional morphology of humans and other species
title_full Hidden diversity: comparative functional morphology of humans and other species
title_fullStr Hidden diversity: comparative functional morphology of humans and other species
title_full_unstemmed Hidden diversity: comparative functional morphology of humans and other species
title_short Hidden diversity: comparative functional morphology of humans and other species
title_sort hidden diversity: comparative functional morphology of humans and other species
topic Anthropology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10135406/
https://www.ncbi.nlm.nih.gov/pubmed/37123005
http://dx.doi.org/10.7717/peerj.15148
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