Cargando…
Quantification of correlational selection on thermal physiology, thermoregulatory behavior, and energy metabolism in lizards
Phenotypic selection is widely accepted as the primary cause of adaptive evolution in natural populations, but selection on complex functional properties linking physiology, behavior, and morphology has been rarely quantified. In ectotherms, correlational selection on thermal physiology, thermoregul...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4567864/ https://www.ncbi.nlm.nih.gov/pubmed/26380689 http://dx.doi.org/10.1002/ece3.1548 |
_version_ | 1782389856116146176 |
---|---|
author | Artacho, Paulina Saravia, Julia Ferrandière, Beatriz Decencière Perret, Samuel Le Galliard, Jean-François |
author_facet | Artacho, Paulina Saravia, Julia Ferrandière, Beatriz Decencière Perret, Samuel Le Galliard, Jean-François |
author_sort | Artacho, Paulina |
collection | PubMed |
description | Phenotypic selection is widely accepted as the primary cause of adaptive evolution in natural populations, but selection on complex functional properties linking physiology, behavior, and morphology has been rarely quantified. In ectotherms, correlational selection on thermal physiology, thermoregulatory behavior, and energy metabolism is of special interest because of their potential coadaptation. We quantified phenotypic selection on thermal sensitivity of locomotor performance (sprint speed), thermal preferences, and resting metabolic rate in captive populations of an ectothermic vertebrate, the common lizard, Zootoca vivipara. No correlational selection between thermal sensitivity of performance, thermoregulatory behavior, and energy metabolism was found. A combination of high body mass and resting metabolic rate was positively correlated with survival and negatively correlated with fecundity. Thus, different mechanisms underlie selection on metabolism in lizards with small body mass than in lizards with high body mass. In addition, lizards that selected the near average preferred body temperature grew faster that their congeners. This is one of the few studies that quantifies significant correlational selection on a proxy of energy expenditure and stabilizing selection on thermoregulatory behavior. |
format | Online Article Text |
id | pubmed-4567864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45678642015-09-17 Quantification of correlational selection on thermal physiology, thermoregulatory behavior, and energy metabolism in lizards Artacho, Paulina Saravia, Julia Ferrandière, Beatriz Decencière Perret, Samuel Le Galliard, Jean-François Ecol Evol Original Research Phenotypic selection is widely accepted as the primary cause of adaptive evolution in natural populations, but selection on complex functional properties linking physiology, behavior, and morphology has been rarely quantified. In ectotherms, correlational selection on thermal physiology, thermoregulatory behavior, and energy metabolism is of special interest because of their potential coadaptation. We quantified phenotypic selection on thermal sensitivity of locomotor performance (sprint speed), thermal preferences, and resting metabolic rate in captive populations of an ectothermic vertebrate, the common lizard, Zootoca vivipara. No correlational selection between thermal sensitivity of performance, thermoregulatory behavior, and energy metabolism was found. A combination of high body mass and resting metabolic rate was positively correlated with survival and negatively correlated with fecundity. Thus, different mechanisms underlie selection on metabolism in lizards with small body mass than in lizards with high body mass. In addition, lizards that selected the near average preferred body temperature grew faster that their congeners. This is one of the few studies that quantifies significant correlational selection on a proxy of energy expenditure and stabilizing selection on thermoregulatory behavior. John Wiley & Sons, Ltd 2015-09 2015-08-07 /pmc/articles/PMC4567864/ /pubmed/26380689 http://dx.doi.org/10.1002/ece3.1548 Text en © 2015 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Artacho, Paulina Saravia, Julia Ferrandière, Beatriz Decencière Perret, Samuel Le Galliard, Jean-François Quantification of correlational selection on thermal physiology, thermoregulatory behavior, and energy metabolism in lizards |
title | Quantification of correlational selection on thermal physiology, thermoregulatory behavior, and energy metabolism in lizards |
title_full | Quantification of correlational selection on thermal physiology, thermoregulatory behavior, and energy metabolism in lizards |
title_fullStr | Quantification of correlational selection on thermal physiology, thermoregulatory behavior, and energy metabolism in lizards |
title_full_unstemmed | Quantification of correlational selection on thermal physiology, thermoregulatory behavior, and energy metabolism in lizards |
title_short | Quantification of correlational selection on thermal physiology, thermoregulatory behavior, and energy metabolism in lizards |
title_sort | quantification of correlational selection on thermal physiology, thermoregulatory behavior, and energy metabolism in lizards |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4567864/ https://www.ncbi.nlm.nih.gov/pubmed/26380689 http://dx.doi.org/10.1002/ece3.1548 |
work_keys_str_mv | AT artachopaulina quantificationofcorrelationalselectiononthermalphysiologythermoregulatorybehaviorandenergymetabolisminlizards AT saraviajulia quantificationofcorrelationalselectiononthermalphysiologythermoregulatorybehaviorandenergymetabolisminlizards AT ferrandierebeatrizdecenciere quantificationofcorrelationalselectiononthermalphysiologythermoregulatorybehaviorandenergymetabolisminlizards AT perretsamuel quantificationofcorrelationalselectiononthermalphysiologythermoregulatorybehaviorandenergymetabolisminlizards AT legalliardjeanfrancois quantificationofcorrelationalselectiononthermalphysiologythermoregulatorybehaviorandenergymetabolisminlizards |