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Natural high pCO(2) increases autotrophy in Anemonia viridis (Anthozoa) as revealed from stable isotope (C, N) analysis
Contemporary cnidarian-algae symbioses are challenged by increasing CO(2) concentrations (ocean warming and acidification) affecting organisms' biological performance. We examined the natural variability of carbon and nitrogen isotopes in the symbiotic sea anemone Anemonia viridis to investigat...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4350107/ https://www.ncbi.nlm.nih.gov/pubmed/25739995 http://dx.doi.org/10.1038/srep08779 |
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author | Horwitz, Rael Borell, Esther M. Yam, Ruth Shemesh, Aldo Fine, Maoz |
author_facet | Horwitz, Rael Borell, Esther M. Yam, Ruth Shemesh, Aldo Fine, Maoz |
author_sort | Horwitz, Rael |
collection | PubMed |
description | Contemporary cnidarian-algae symbioses are challenged by increasing CO(2) concentrations (ocean warming and acidification) affecting organisms' biological performance. We examined the natural variability of carbon and nitrogen isotopes in the symbiotic sea anemone Anemonia viridis to investigate dietary shifts (autotrophy/heterotrophy) along a natural pCO(2) gradient at the island of Vulcano, Italy. δ(13)C values for both algal symbionts (Symbiodinium) and host tissue of A. viridis became significantly lighter with increasing seawater pCO(2). Together with a decrease in the difference between δ(13)C values of both fractions at the higher pCO(2) sites, these results indicate there is a greater net autotrophic input to the A. viridis carbon budget under high pCO(2) conditions. δ(15)N values and C/N ratios did not change in Symbiodinium and host tissue along the pCO(2) gradient. Additional physiological parameters revealed anemone protein and Symbiodinium chlorophyll a remained unaltered among sites. Symbiodinium density was similar among sites yet their mitotic index increased in anemones under elevated pCO(2). Overall, our findings show that A. viridis is characterized by a higher autotrophic/heterotrophic ratio as pCO(2) increases. The unique trophic flexibility of this species may give it a competitive advantage and enable its potential acclimation and ecological success in the future under increased ocean acidification. |
format | Online Article Text |
id | pubmed-4350107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43501072015-03-10 Natural high pCO(2) increases autotrophy in Anemonia viridis (Anthozoa) as revealed from stable isotope (C, N) analysis Horwitz, Rael Borell, Esther M. Yam, Ruth Shemesh, Aldo Fine, Maoz Sci Rep Article Contemporary cnidarian-algae symbioses are challenged by increasing CO(2) concentrations (ocean warming and acidification) affecting organisms' biological performance. We examined the natural variability of carbon and nitrogen isotopes in the symbiotic sea anemone Anemonia viridis to investigate dietary shifts (autotrophy/heterotrophy) along a natural pCO(2) gradient at the island of Vulcano, Italy. δ(13)C values for both algal symbionts (Symbiodinium) and host tissue of A. viridis became significantly lighter with increasing seawater pCO(2). Together with a decrease in the difference between δ(13)C values of both fractions at the higher pCO(2) sites, these results indicate there is a greater net autotrophic input to the A. viridis carbon budget under high pCO(2) conditions. δ(15)N values and C/N ratios did not change in Symbiodinium and host tissue along the pCO(2) gradient. Additional physiological parameters revealed anemone protein and Symbiodinium chlorophyll a remained unaltered among sites. Symbiodinium density was similar among sites yet their mitotic index increased in anemones under elevated pCO(2). Overall, our findings show that A. viridis is characterized by a higher autotrophic/heterotrophic ratio as pCO(2) increases. The unique trophic flexibility of this species may give it a competitive advantage and enable its potential acclimation and ecological success in the future under increased ocean acidification. Nature Publishing Group 2015-03-05 /pmc/articles/PMC4350107/ /pubmed/25739995 http://dx.doi.org/10.1038/srep08779 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Horwitz, Rael Borell, Esther M. Yam, Ruth Shemesh, Aldo Fine, Maoz Natural high pCO(2) increases autotrophy in Anemonia viridis (Anthozoa) as revealed from stable isotope (C, N) analysis |
title | Natural high pCO(2) increases autotrophy in Anemonia viridis (Anthozoa) as revealed from stable isotope (C, N) analysis |
title_full | Natural high pCO(2) increases autotrophy in Anemonia viridis (Anthozoa) as revealed from stable isotope (C, N) analysis |
title_fullStr | Natural high pCO(2) increases autotrophy in Anemonia viridis (Anthozoa) as revealed from stable isotope (C, N) analysis |
title_full_unstemmed | Natural high pCO(2) increases autotrophy in Anemonia viridis (Anthozoa) as revealed from stable isotope (C, N) analysis |
title_short | Natural high pCO(2) increases autotrophy in Anemonia viridis (Anthozoa) as revealed from stable isotope (C, N) analysis |
title_sort | natural high pco(2) increases autotrophy in anemonia viridis (anthozoa) as revealed from stable isotope (c, n) analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4350107/ https://www.ncbi.nlm.nih.gov/pubmed/25739995 http://dx.doi.org/10.1038/srep08779 |
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