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Feeding and thermal conditioning enhance coral temperature tolerance in juvenile Pocillopora acuta

Scleractinian corals form the foundation of coral reefs by acquiring autotrophic nutrition from photosynthetic endosymbionts (Symbiodiniaceae) and use feeding to obtain additional nutrition, especially when the symbiosis is compromised (i.e. bleaching). Juvenile corals are vulnerable to stress due t...

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Autores principales: Huffmyer, Ariana S., Johnson, Colton J., Epps, Ashleigh M., Lemus, Judith D., Gates, Ruth D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150050/
https://www.ncbi.nlm.nih.gov/pubmed/34084554
http://dx.doi.org/10.1098/rsos.210644
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author Huffmyer, Ariana S.
Johnson, Colton J.
Epps, Ashleigh M.
Lemus, Judith D.
Gates, Ruth D.
author_facet Huffmyer, Ariana S.
Johnson, Colton J.
Epps, Ashleigh M.
Lemus, Judith D.
Gates, Ruth D.
author_sort Huffmyer, Ariana S.
collection PubMed
description Scleractinian corals form the foundation of coral reefs by acquiring autotrophic nutrition from photosynthetic endosymbionts (Symbiodiniaceae) and use feeding to obtain additional nutrition, especially when the symbiosis is compromised (i.e. bleaching). Juvenile corals are vulnerable to stress due to low energetic reserves and high demand for growth, which is compounded when additional stressors occur. Therefore, conditions that favour energy acquisition and storage may enhance survival under stressful conditions. To investigate the influence of feeding on thermal tolerance, we exposed Pocillopora acuta juveniles to temperature (ambient, 27.4°C versus cool, 25.9°C) and feeding treatments (fed versus unfed) for 30 days post-settlement and monitored growth and physiology, followed by tracking survival under thermal stress. Feeding increased growth and resulted in thicker tissues and elevated symbiont fluorescence. Under high-temperature stress (31–60 days post-settlement; ca 30.1°C), corals that were fed and previously exposed to cool temperature had 33% higher survival than other treatment groups. These corals demonstrated reduced symbiont fluorescence, which may have provided protective effects under thermal stress. These results highlight that the impacts of feeding on coral physiology and stress tolerance are dependent on temperature and as oceans continue to warm, early life stages may experience shifts in feeding strategies to survive.
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spelling pubmed-81500502021-06-02 Feeding and thermal conditioning enhance coral temperature tolerance in juvenile Pocillopora acuta Huffmyer, Ariana S. Johnson, Colton J. Epps, Ashleigh M. Lemus, Judith D. Gates, Ruth D. R Soc Open Sci Ecology, Conservation, and Global Change Biology Scleractinian corals form the foundation of coral reefs by acquiring autotrophic nutrition from photosynthetic endosymbionts (Symbiodiniaceae) and use feeding to obtain additional nutrition, especially when the symbiosis is compromised (i.e. bleaching). Juvenile corals are vulnerable to stress due to low energetic reserves and high demand for growth, which is compounded when additional stressors occur. Therefore, conditions that favour energy acquisition and storage may enhance survival under stressful conditions. To investigate the influence of feeding on thermal tolerance, we exposed Pocillopora acuta juveniles to temperature (ambient, 27.4°C versus cool, 25.9°C) and feeding treatments (fed versus unfed) for 30 days post-settlement and monitored growth and physiology, followed by tracking survival under thermal stress. Feeding increased growth and resulted in thicker tissues and elevated symbiont fluorescence. Under high-temperature stress (31–60 days post-settlement; ca 30.1°C), corals that were fed and previously exposed to cool temperature had 33% higher survival than other treatment groups. These corals demonstrated reduced symbiont fluorescence, which may have provided protective effects under thermal stress. These results highlight that the impacts of feeding on coral physiology and stress tolerance are dependent on temperature and as oceans continue to warm, early life stages may experience shifts in feeding strategies to survive. The Royal Society 2021-05-26 /pmc/articles/PMC8150050/ /pubmed/34084554 http://dx.doi.org/10.1098/rsos.210644 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Ecology, Conservation, and Global Change Biology
Huffmyer, Ariana S.
Johnson, Colton J.
Epps, Ashleigh M.
Lemus, Judith D.
Gates, Ruth D.
Feeding and thermal conditioning enhance coral temperature tolerance in juvenile Pocillopora acuta
title Feeding and thermal conditioning enhance coral temperature tolerance in juvenile Pocillopora acuta
title_full Feeding and thermal conditioning enhance coral temperature tolerance in juvenile Pocillopora acuta
title_fullStr Feeding and thermal conditioning enhance coral temperature tolerance in juvenile Pocillopora acuta
title_full_unstemmed Feeding and thermal conditioning enhance coral temperature tolerance in juvenile Pocillopora acuta
title_short Feeding and thermal conditioning enhance coral temperature tolerance in juvenile Pocillopora acuta
title_sort feeding and thermal conditioning enhance coral temperature tolerance in juvenile pocillopora acuta
topic Ecology, Conservation, and Global Change Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150050/
https://www.ncbi.nlm.nih.gov/pubmed/34084554
http://dx.doi.org/10.1098/rsos.210644
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