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Haematological traits co-vary with migratory status, altitude and energy expenditure: a phylogenetic, comparative analysis

Aerobic capacity is assumed to be a main predictor of workload ability and haematocrit (Hct) and haemoglobin (Hb) have been suggested as key determinants of aerobic performance. Intraspecific studies have reported increases in Hct and Hb in response to increased workload. Furthermore, Hct and Hb var...

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Autores principales: Yap, Kang Nian, Tsai, Olivia Hsin-I, Williams, Tony D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6476874/
https://www.ncbi.nlm.nih.gov/pubmed/31011157
http://dx.doi.org/10.1038/s41598-019-42921-4
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author Yap, Kang Nian
Tsai, Olivia Hsin-I
Williams, Tony D.
author_facet Yap, Kang Nian
Tsai, Olivia Hsin-I
Williams, Tony D.
author_sort Yap, Kang Nian
collection PubMed
description Aerobic capacity is assumed to be a main predictor of workload ability and haematocrit (Hct) and haemoglobin (Hb) have been suggested as key determinants of aerobic performance. Intraspecific studies have reported increases in Hct and Hb in response to increased workload. Furthermore, Hct and Hb vary markedly among individuals and throughout the annual cycle in free-living birds and it has been suggested that this variation reflects adaptive modulation of these traits to meet seasonal changes in energy demands. We used a comparative dataset of haematological traits, measures of metabolic rate (57 species), and life-history traits (160 species) to test several hypotheses for adaptive variation in haematology in relation to migration and altitude. We then extended these general ideas to test relationships between Hct and basal metabolic rate, daily energy expenditure and activity energy expenditure, using the 57 species that we have metabolic rate information for. We found that at the interspecific level, full migrants have higher Hct and Hb than partial migrants and non-migrants, and that altitude is positively correlated with Hb but not Hct. Hct is positively associated with activity energy expenditure (energy spent specifically on costly activities), suggesting that haematological traits could be adaptively modulated based on life-history traits and that Hct is a potential physiological mediator of energetic constraint.
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spelling pubmed-64768742019-05-02 Haematological traits co-vary with migratory status, altitude and energy expenditure: a phylogenetic, comparative analysis Yap, Kang Nian Tsai, Olivia Hsin-I Williams, Tony D. Sci Rep Article Aerobic capacity is assumed to be a main predictor of workload ability and haematocrit (Hct) and haemoglobin (Hb) have been suggested as key determinants of aerobic performance. Intraspecific studies have reported increases in Hct and Hb in response to increased workload. Furthermore, Hct and Hb vary markedly among individuals and throughout the annual cycle in free-living birds and it has been suggested that this variation reflects adaptive modulation of these traits to meet seasonal changes in energy demands. We used a comparative dataset of haematological traits, measures of metabolic rate (57 species), and life-history traits (160 species) to test several hypotheses for adaptive variation in haematology in relation to migration and altitude. We then extended these general ideas to test relationships between Hct and basal metabolic rate, daily energy expenditure and activity energy expenditure, using the 57 species that we have metabolic rate information for. We found that at the interspecific level, full migrants have higher Hct and Hb than partial migrants and non-migrants, and that altitude is positively correlated with Hb but not Hct. Hct is positively associated with activity energy expenditure (energy spent specifically on costly activities), suggesting that haematological traits could be adaptively modulated based on life-history traits and that Hct is a potential physiological mediator of energetic constraint. Nature Publishing Group UK 2019-04-23 /pmc/articles/PMC6476874/ /pubmed/31011157 http://dx.doi.org/10.1038/s41598-019-42921-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yap, Kang Nian
Tsai, Olivia Hsin-I
Williams, Tony D.
Haematological traits co-vary with migratory status, altitude and energy expenditure: a phylogenetic, comparative analysis
title Haematological traits co-vary with migratory status, altitude and energy expenditure: a phylogenetic, comparative analysis
title_full Haematological traits co-vary with migratory status, altitude and energy expenditure: a phylogenetic, comparative analysis
title_fullStr Haematological traits co-vary with migratory status, altitude and energy expenditure: a phylogenetic, comparative analysis
title_full_unstemmed Haematological traits co-vary with migratory status, altitude and energy expenditure: a phylogenetic, comparative analysis
title_short Haematological traits co-vary with migratory status, altitude and energy expenditure: a phylogenetic, comparative analysis
title_sort haematological traits co-vary with migratory status, altitude and energy expenditure: a phylogenetic, comparative analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6476874/
https://www.ncbi.nlm.nih.gov/pubmed/31011157
http://dx.doi.org/10.1038/s41598-019-42921-4
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