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Behavioural and physiological adaptations to low-temperature environments in the common frog, Rana temporaria
BACKGROUND: Extreme environments can impose strong ecological and evolutionary pressures at a local level. Ectotherms are particularly sensitive to low-temperature environments, which can result in a reduced activity period, slowed physiological processes and increased exposure to sub-zero temperatu...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4037278/ https://www.ncbi.nlm.nih.gov/pubmed/24885261 http://dx.doi.org/10.1186/1471-2148-14-110 |
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author | Muir, Anna P Biek, Roman Mable, Barbara K |
author_facet | Muir, Anna P Biek, Roman Mable, Barbara K |
author_sort | Muir, Anna P |
collection | PubMed |
description | BACKGROUND: Extreme environments can impose strong ecological and evolutionary pressures at a local level. Ectotherms are particularly sensitive to low-temperature environments, which can result in a reduced activity period, slowed physiological processes and increased exposure to sub-zero temperatures. The aim of this study was to assess the behavioural and physiological responses that facilitate survival in low-temperature environments. In particular, we asked: 1) do high-altitude common frog (Rana temporaria) adults extend the time available for larval growth by breeding at lower temperatures than low-altitude individuals?; and 2) do tadpoles sampled from high-altitude sites differ physiologically from those from low-altitude sites, in terms of routine metabolic rate (RMR) and freeze tolerance? Breeding date was assessed as the first day of spawn observation and local temperature recorded for five, paired high- and low-altitude R. temporaria breeding sites in Scotland. Spawn was collected and tadpoles raised in a common laboratory environment, where RMR was measured as oxygen consumed using a closed respiratory tube system. Freeze tolerance was measured as survival following slow cooling to the point when all container water had frozen. RESULTS: We found that breeding did not occur below 5°C at any site and there was no significant relationship between breeding temperature and altitude, leading to a delay in spawning of five days for every 100 m increase in altitude. The relationship between altitude and RMR varied by mountain but was lower for individuals sampled from high- than low-altitude sites within the three mountains with the highest high-altitude sites (≥900 m). In contrast, individuals sampled from low-altitudes survived freezing significantly better than those from high-altitudes, across all mountains. CONCLUSIONS: Our results suggest that adults at high-altitude do not show behavioural adaptations in terms of breeding at lower temperatures. However, tadpoles appear to have the potential to adapt physiologically to surviving at high-altitude via reduced RMR but without an increase in freeze tolerance. Therefore, survival at high-altitude may be facilitated by physiological mechanisms that permit faster growth rates, allowing completion of larval development within a shorter time period, alleviating the need for adaptations that extend the time available for larval growth. |
format | Online Article Text |
id | pubmed-4037278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40372782014-05-29 Behavioural and physiological adaptations to low-temperature environments in the common frog, Rana temporaria Muir, Anna P Biek, Roman Mable, Barbara K BMC Evol Biol Research Article BACKGROUND: Extreme environments can impose strong ecological and evolutionary pressures at a local level. Ectotherms are particularly sensitive to low-temperature environments, which can result in a reduced activity period, slowed physiological processes and increased exposure to sub-zero temperatures. The aim of this study was to assess the behavioural and physiological responses that facilitate survival in low-temperature environments. In particular, we asked: 1) do high-altitude common frog (Rana temporaria) adults extend the time available for larval growth by breeding at lower temperatures than low-altitude individuals?; and 2) do tadpoles sampled from high-altitude sites differ physiologically from those from low-altitude sites, in terms of routine metabolic rate (RMR) and freeze tolerance? Breeding date was assessed as the first day of spawn observation and local temperature recorded for five, paired high- and low-altitude R. temporaria breeding sites in Scotland. Spawn was collected and tadpoles raised in a common laboratory environment, where RMR was measured as oxygen consumed using a closed respiratory tube system. Freeze tolerance was measured as survival following slow cooling to the point when all container water had frozen. RESULTS: We found that breeding did not occur below 5°C at any site and there was no significant relationship between breeding temperature and altitude, leading to a delay in spawning of five days for every 100 m increase in altitude. The relationship between altitude and RMR varied by mountain but was lower for individuals sampled from high- than low-altitude sites within the three mountains with the highest high-altitude sites (≥900 m). In contrast, individuals sampled from low-altitudes survived freezing significantly better than those from high-altitudes, across all mountains. CONCLUSIONS: Our results suggest that adults at high-altitude do not show behavioural adaptations in terms of breeding at lower temperatures. However, tadpoles appear to have the potential to adapt physiologically to surviving at high-altitude via reduced RMR but without an increase in freeze tolerance. Therefore, survival at high-altitude may be facilitated by physiological mechanisms that permit faster growth rates, allowing completion of larval development within a shorter time period, alleviating the need for adaptations that extend the time available for larval growth. BioMed Central 2014-05-23 /pmc/articles/PMC4037278/ /pubmed/24885261 http://dx.doi.org/10.1186/1471-2148-14-110 Text en Copyright © 2014 Muir et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Muir, Anna P Biek, Roman Mable, Barbara K Behavioural and physiological adaptations to low-temperature environments in the common frog, Rana temporaria |
title | Behavioural and physiological adaptations to low-temperature environments in the common frog, Rana temporaria |
title_full | Behavioural and physiological adaptations to low-temperature environments in the common frog, Rana temporaria |
title_fullStr | Behavioural and physiological adaptations to low-temperature environments in the common frog, Rana temporaria |
title_full_unstemmed | Behavioural and physiological adaptations to low-temperature environments in the common frog, Rana temporaria |
title_short | Behavioural and physiological adaptations to low-temperature environments in the common frog, Rana temporaria |
title_sort | behavioural and physiological adaptations to low-temperature environments in the common frog, rana temporaria |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4037278/ https://www.ncbi.nlm.nih.gov/pubmed/24885261 http://dx.doi.org/10.1186/1471-2148-14-110 |
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