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The trade-off between heat tolerance and metabolic cost drives the bimodal life strategy at the air-water interface
The principle of oxygen and capacity limitation of thermal tolerance in ectotherms suggests that the long-term upper limits of an organism's thermal niche are equivalent to the upper limits of the organism's functional capacity for oxygen provision to tissues. Air-breathing ectotherms show...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725839/ https://www.ncbi.nlm.nih.gov/pubmed/26758742 http://dx.doi.org/10.1038/srep19158 |
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author | Fusi, Marco Cannicci, Stefano Daffonchio, Daniele Mostert, Bruce Pörtner, Hans-Otto Giomi, Folco |
author_facet | Fusi, Marco Cannicci, Stefano Daffonchio, Daniele Mostert, Bruce Pörtner, Hans-Otto Giomi, Folco |
author_sort | Fusi, Marco |
collection | PubMed |
description | The principle of oxygen and capacity limitation of thermal tolerance in ectotherms suggests that the long-term upper limits of an organism's thermal niche are equivalent to the upper limits of the organism's functional capacity for oxygen provision to tissues. Air-breathing ectotherms show wider thermal tolerances, since they can take advantage of the higher availability of oxygen in air than in water. Bimodal species move from aquatic to aerial media and switch between habitats in response to environmental variations such as cyclical or anomalous temperature fluctuations. Here we tested the prediction that bimodal species cope better with thermal stress than truly aquatic species using the crab Pachygrapsus marmoratus as a model species. When in water, oxygen consumption rates of P. marmoratus acutely rise during warming. Beyond a temperature threshold of 23 °C the crab's aerobic metabolism in air remains lower than in water. In parallel, the haemolymph oxygen partial pressure of submerged animals progressive decreases during warming, while it remains low but constant during emersion. Our results demonstrate the ability of a bimodal breathing ectotherm to extend its thermal tolerance during air-breathing, suggesting that there are temperature-related physiological benefits during the evolution of the bimodal life style. |
format | Online Article Text |
id | pubmed-4725839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47258392016-01-28 The trade-off between heat tolerance and metabolic cost drives the bimodal life strategy at the air-water interface Fusi, Marco Cannicci, Stefano Daffonchio, Daniele Mostert, Bruce Pörtner, Hans-Otto Giomi, Folco Sci Rep Article The principle of oxygen and capacity limitation of thermal tolerance in ectotherms suggests that the long-term upper limits of an organism's thermal niche are equivalent to the upper limits of the organism's functional capacity for oxygen provision to tissues. Air-breathing ectotherms show wider thermal tolerances, since they can take advantage of the higher availability of oxygen in air than in water. Bimodal species move from aquatic to aerial media and switch between habitats in response to environmental variations such as cyclical or anomalous temperature fluctuations. Here we tested the prediction that bimodal species cope better with thermal stress than truly aquatic species using the crab Pachygrapsus marmoratus as a model species. When in water, oxygen consumption rates of P. marmoratus acutely rise during warming. Beyond a temperature threshold of 23 °C the crab's aerobic metabolism in air remains lower than in water. In parallel, the haemolymph oxygen partial pressure of submerged animals progressive decreases during warming, while it remains low but constant during emersion. Our results demonstrate the ability of a bimodal breathing ectotherm to extend its thermal tolerance during air-breathing, suggesting that there are temperature-related physiological benefits during the evolution of the bimodal life style. Nature Publishing Group 2016-01-13 /pmc/articles/PMC4725839/ /pubmed/26758742 http://dx.doi.org/10.1038/srep19158 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Fusi, Marco Cannicci, Stefano Daffonchio, Daniele Mostert, Bruce Pörtner, Hans-Otto Giomi, Folco The trade-off between heat tolerance and metabolic cost drives the bimodal life strategy at the air-water interface |
title | The trade-off between heat tolerance and metabolic cost drives the bimodal life strategy at the air-water interface |
title_full | The trade-off between heat tolerance and metabolic cost drives the bimodal life strategy at the air-water interface |
title_fullStr | The trade-off between heat tolerance and metabolic cost drives the bimodal life strategy at the air-water interface |
title_full_unstemmed | The trade-off between heat tolerance and metabolic cost drives the bimodal life strategy at the air-water interface |
title_short | The trade-off between heat tolerance and metabolic cost drives the bimodal life strategy at the air-water interface |
title_sort | trade-off between heat tolerance and metabolic cost drives the bimodal life strategy at the air-water interface |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725839/ https://www.ncbi.nlm.nih.gov/pubmed/26758742 http://dx.doi.org/10.1038/srep19158 |
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