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Nutritional input from dinoflagellate symbionts in reef-building corals is minimal during planula larval life stage
Dispersion of larval offspring is of fundamental ecological importance to sessile marine organisms. Photosymbiotic planulae emitted by many reef-forming corals may travel over large distances before settling to form a new colony. It is not clear whether the metabolic requirements of these planula la...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820372/ https://www.ncbi.nlm.nih.gov/pubmed/27051861 http://dx.doi.org/10.1126/sciadv.1500681 |
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author | Kopp, Christophe Domart-Coulon, Isabelle Barthelemy, Dominique Meibom, Anders |
author_facet | Kopp, Christophe Domart-Coulon, Isabelle Barthelemy, Dominique Meibom, Anders |
author_sort | Kopp, Christophe |
collection | PubMed |
description | Dispersion of larval offspring is of fundamental ecological importance to sessile marine organisms. Photosymbiotic planulae emitted by many reef-forming corals may travel over large distances before settling to form a new colony. It is not clear whether the metabolic requirements of these planula larvae are met exclusively with lipid and protein reservoirs inherited from the mother colony or when metabolic inputs from their endosymbiotic dinoflagellates become important. Pulse-chase experiments using [(13)C]bicarbonate and [(15)N]nitrate, combined with subcellular structural and isotopic imaging of freshly emitted symbiotic larvae from the coral Pocillopora damicornis, show that metabolic input from the dinoflagellates is minimal in the planulae compared with adult colonies. The larvae are essentially lecithotrophic upon emission, indicating that a marked shift in metabolic interaction between the symbiotic partners takes place later during ontogeny. Understanding the cellular processes that trigger and control this metabolic shift, and how climate change might influence it, is a key challenge in coral biology. |
format | Online Article Text |
id | pubmed-4820372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48203722016-04-05 Nutritional input from dinoflagellate symbionts in reef-building corals is minimal during planula larval life stage Kopp, Christophe Domart-Coulon, Isabelle Barthelemy, Dominique Meibom, Anders Sci Adv Research Articles Dispersion of larval offspring is of fundamental ecological importance to sessile marine organisms. Photosymbiotic planulae emitted by many reef-forming corals may travel over large distances before settling to form a new colony. It is not clear whether the metabolic requirements of these planula larvae are met exclusively with lipid and protein reservoirs inherited from the mother colony or when metabolic inputs from their endosymbiotic dinoflagellates become important. Pulse-chase experiments using [(13)C]bicarbonate and [(15)N]nitrate, combined with subcellular structural and isotopic imaging of freshly emitted symbiotic larvae from the coral Pocillopora damicornis, show that metabolic input from the dinoflagellates is minimal in the planulae compared with adult colonies. The larvae are essentially lecithotrophic upon emission, indicating that a marked shift in metabolic interaction between the symbiotic partners takes place later during ontogeny. Understanding the cellular processes that trigger and control this metabolic shift, and how climate change might influence it, is a key challenge in coral biology. American Association for the Advancement of Science 2016-03-25 /pmc/articles/PMC4820372/ /pubmed/27051861 http://dx.doi.org/10.1126/sciadv.1500681 Text en Copyright © 2016, The Authors http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Kopp, Christophe Domart-Coulon, Isabelle Barthelemy, Dominique Meibom, Anders Nutritional input from dinoflagellate symbionts in reef-building corals is minimal during planula larval life stage |
title | Nutritional input from dinoflagellate symbionts in reef-building corals is minimal during planula larval life stage |
title_full | Nutritional input from dinoflagellate symbionts in reef-building corals is minimal during planula larval life stage |
title_fullStr | Nutritional input from dinoflagellate symbionts in reef-building corals is minimal during planula larval life stage |
title_full_unstemmed | Nutritional input from dinoflagellate symbionts in reef-building corals is minimal during planula larval life stage |
title_short | Nutritional input from dinoflagellate symbionts in reef-building corals is minimal during planula larval life stage |
title_sort | nutritional input from dinoflagellate symbionts in reef-building corals is minimal during planula larval life stage |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820372/ https://www.ncbi.nlm.nih.gov/pubmed/27051861 http://dx.doi.org/10.1126/sciadv.1500681 |
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