Major cellular and physiological impacts of ocean acidification on a reef building coral.
As atmospheric levels of CO(2) increase, reef-building corals are under greater stress from both increased sea surface temperatures and declining sea water pH. To date, most studies have focused on either coral bleaching due to warming oceans or declining calcification due to decreasing oceanic carb...
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Public Library of Science (PLoS)
2012
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oai:doaj.org-article:0c7f0e972cff44bda6fb7c58468540db2021-11-18T07:22:38ZMajor cellular and physiological impacts of ocean acidification on a reef building coral.1932-620310.1371/journal.pone.0034659https://doaj.org/article/0c7f0e972cff44bda6fb7c58468540db2012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22509341/?tool=EBIhttps://doaj.org/toc/1932-6203As atmospheric levels of CO(2) increase, reef-building corals are under greater stress from both increased sea surface temperatures and declining sea water pH. To date, most studies have focused on either coral bleaching due to warming oceans or declining calcification due to decreasing oceanic carbonate ion concentrations. Here, through the use of physiology measurements and cDNA microarrays, we show that changes in pH and ocean chemistry consistent with two scenarios put forward by the Intergovernmental Panel on Climate Change (IPCC) drive major changes in gene expression, respiration, photosynthesis and symbiosis of the coral, Acropora millepora, before affects on biomineralisation are apparent at the phenotype level. Under high CO(2) conditions corals at the phenotype level lost over half their Symbiodinium populations, and had a decrease in both photosynthesis and respiration. Changes in gene expression were consistent with metabolic suppression, an increase in oxidative stress, apoptosis and symbiont loss. Other expression patterns demonstrate upregulation of membrane transporters, as well as the regulation of genes involved in membrane cytoskeletal interactions and cytoskeletal remodeling. These widespread changes in gene expression emphasize the need to expand future studies of ocean acidification to include a wider spectrum of cellular processes, many of which may occur before impacts on calcification.Paulina KaniewskaPaul R CampbellDavid I KlineMauricio Rodriguez-LanettyDavid J MillerSophie DoveOve Hoegh-GuldbergPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 4, p e34659 (2012) |
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Medicine R Science Q Paulina Kaniewska Paul R Campbell David I Kline Mauricio Rodriguez-Lanetty David J Miller Sophie Dove Ove Hoegh-Guldberg Major cellular and physiological impacts of ocean acidification on a reef building coral. |
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As atmospheric levels of CO(2) increase, reef-building corals are under greater stress from both increased sea surface temperatures and declining sea water pH. To date, most studies have focused on either coral bleaching due to warming oceans or declining calcification due to decreasing oceanic carbonate ion concentrations. Here, through the use of physiology measurements and cDNA microarrays, we show that changes in pH and ocean chemistry consistent with two scenarios put forward by the Intergovernmental Panel on Climate Change (IPCC) drive major changes in gene expression, respiration, photosynthesis and symbiosis of the coral, Acropora millepora, before affects on biomineralisation are apparent at the phenotype level. Under high CO(2) conditions corals at the phenotype level lost over half their Symbiodinium populations, and had a decrease in both photosynthesis and respiration. Changes in gene expression were consistent with metabolic suppression, an increase in oxidative stress, apoptosis and symbiont loss. Other expression patterns demonstrate upregulation of membrane transporters, as well as the regulation of genes involved in membrane cytoskeletal interactions and cytoskeletal remodeling. These widespread changes in gene expression emphasize the need to expand future studies of ocean acidification to include a wider spectrum of cellular processes, many of which may occur before impacts on calcification. |
format |
article |
author |
Paulina Kaniewska Paul R Campbell David I Kline Mauricio Rodriguez-Lanetty David J Miller Sophie Dove Ove Hoegh-Guldberg |
author_facet |
Paulina Kaniewska Paul R Campbell David I Kline Mauricio Rodriguez-Lanetty David J Miller Sophie Dove Ove Hoegh-Guldberg |
author_sort |
Paulina Kaniewska |
title |
Major cellular and physiological impacts of ocean acidification on a reef building coral. |
title_short |
Major cellular and physiological impacts of ocean acidification on a reef building coral. |
title_full |
Major cellular and physiological impacts of ocean acidification on a reef building coral. |
title_fullStr |
Major cellular and physiological impacts of ocean acidification on a reef building coral. |
title_full_unstemmed |
Major cellular and physiological impacts of ocean acidification on a reef building coral. |
title_sort |
major cellular and physiological impacts of ocean acidification on a reef building coral. |
publisher |
Public Library of Science (PLoS) |
publishDate |
2012 |
url |
https://doaj.org/article/0c7f0e972cff44bda6fb7c58468540db |
work_keys_str_mv |
AT paulinakaniewska majorcellularandphysiologicalimpactsofoceanacidificationonareefbuildingcoral AT paulrcampbell majorcellularandphysiologicalimpactsofoceanacidificationonareefbuildingcoral AT davidikline majorcellularandphysiologicalimpactsofoceanacidificationonareefbuildingcoral AT mauriciorodriguezlanetty majorcellularandphysiologicalimpactsofoceanacidificationonareefbuildingcoral AT davidjmiller majorcellularandphysiologicalimpactsofoceanacidificationonareefbuildingcoral AT sophiedove majorcellularandphysiologicalimpactsofoceanacidificationonareefbuildingcoral AT ovehoeghguldberg majorcellularandphysiologicalimpactsofoceanacidificationonareefbuildingcoral |
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1718423516923035648 |