id ftpangaea:oai:pangaea.de:doi:10.1594/PANGAEA.837880
record_format openpolar
spelling ftpangaea:oai:pangaea.de:doi:10.1594/PANGAEA.837880 2023-05-15T17:52:09+02:00 Adaptation of a globally important coccolithophore to ocean warming and acidification Gibbin, Emma M Putnam, H M Davy, Simon K Gates, Ruth D 2014-11-04 text/tab-separated-values, 3840 data points https://doi.pangaea.de/10.1594/PANGAEA.837880 https://doi.org/10.1594/PANGAEA.837880 en eng PANGAEA Lavigne, Héloïse; Epitalon, Jean-Marie; Gattuso, Jean-Pierre (2014): seacarb: seawater carbonate chemistry with R. R package version 3.0. https://cran.r-project.org/package=seacarb https://doi.pangaea.de/10.1594/PANGAEA.837880 https://doi.org/10.1594/PANGAEA.837880 CC-BY-3.0: Creative Commons Attribution 3.0 Unported Access constraints: unrestricted info:eu-repo/semantics/openAccess CC-BY Supplement to: Gibbin, Emma M; Putnam, H M; Davy, Simon K; Gates, Ruth D (2014): Intracellular pH and its response to CO2-driven seawater acidification in symbiotic versus non-symbiotic coral cells. Journal of Experimental Biology, 217(11), 1963-1969, https://doi.org/10.1242/jeb.099549 Acid-base regulation Alkalinity total standard error Animalia Aragonite saturation state Benthic animals Benthos Bicarbonate ion Calcite saturation state Calculated using seacarb after Nisumaa et al. (2010) Carbon inorganic dissolved Carbonate ion Carbonate system computation flag Carbon dioxide Cnidaria Coast and continental shelf Containers and aquaria (20-1000 L or < 1 m**2) Figure Fugacity of carbon dioxide (water) at sea surface temperature (wet air) Laboratory experiment North Pacific OA-ICC Ocean Acidification International Coordination Centre Partial pressure of carbon dioxide (water) at sea surface temperature (wet air) pH extracellular intracellular pH change Pocillopora damicornis Replicate Salinity Single species Species Temperature water Time in minutes Dataset 2014 ftpangaea https://doi.org/10.1594/PANGAEA.837880 https://doi.org/10.1242/jeb.099549 2023-01-20T09:04:17Z Regulating intracellular pH (pHi) is critical for optimising the metabolic activity of corals, yet mechanisms involved in pH regulation and the buffering capacity within coral cells are not well understood. Our study investigated how the presence of symbiotic dinoflagellates affects the response of pHi to pCO2-driven seawater acidification in cells isolated from Pocillopora damicornis. Using the fluorescent dye BCECF-AM, in conjunction with confocal microscopy, we simultaneously characterised the response of pHi in host coral cells and their dinoflagellate symbionts, in symbiotic and non-symbiotic states under saturating light, with and without the photosynthetic inhibitor DCMU. Each treatment was run under control (pH 7.8) and CO2 acidified seawater conditions (decreasing pH from 7.8 - 6.8). After two hours of CO2 addition, by which time the external pH (pHe) had declined to 6.8, the dinoflagellate symbionts had increased their pHi by 0.5 pH units above control levels. In contrast, in both symbiotic and non-symbiotic host coral cells, 15 min of CO2 addition (0.2 pH unit drop in pHe) led to cytoplasmic acidosis equivalent to 0.4 pH units. Despite further seawater acidification over the duration of the experiment, the pHi of non-symbiotic coral cells did not change, though in host cells containing a symbiont cell the pHi recovered to control levels. This recovery was negated when cells were incubated with DCMU. Our results reveal that photosynthetic activity of the endosymbiont is tightly coupled with the ability of the host cell to recover from cellular acidosis after exposure to high CO2 / low pH. Dataset Ocean acidification PANGAEA - Data Publisher for Earth & Environmental Science Pacific
institution Open Polar
collection PANGAEA - Data Publisher for Earth & Environmental Science
op_collection_id ftpangaea
language English
topic Acid-base regulation
Alkalinity
total
standard error
Animalia
Aragonite saturation state
Benthic animals
Benthos
Bicarbonate ion
Calcite saturation state
Calculated using seacarb after Nisumaa et al. (2010)
Carbon
inorganic
dissolved
Carbonate ion
Carbonate system computation flag
Carbon dioxide
Cnidaria
Coast and continental shelf
Containers and aquaria (20-1000 L or < 1 m**2)
Figure
Fugacity of carbon dioxide (water) at sea surface temperature (wet air)
Laboratory experiment
North Pacific
OA-ICC
Ocean Acidification International Coordination Centre
Partial pressure of carbon dioxide (water) at sea surface temperature (wet air)
pH
extracellular
intracellular
pH change
Pocillopora damicornis
Replicate
Salinity
Single species
Species
Temperature
water
Time in minutes
spellingShingle Acid-base regulation
Alkalinity
total
standard error
Animalia
Aragonite saturation state
Benthic animals
Benthos
Bicarbonate ion
Calcite saturation state
Calculated using seacarb after Nisumaa et al. (2010)
Carbon
inorganic
dissolved
Carbonate ion
Carbonate system computation flag
Carbon dioxide
Cnidaria
Coast and continental shelf
Containers and aquaria (20-1000 L or < 1 m**2)
Figure
Fugacity of carbon dioxide (water) at sea surface temperature (wet air)
Laboratory experiment
North Pacific
OA-ICC
Ocean Acidification International Coordination Centre
Partial pressure of carbon dioxide (water) at sea surface temperature (wet air)
pH
extracellular
intracellular
pH change
Pocillopora damicornis
Replicate
Salinity
Single species
Species
Temperature
water
Time in minutes
Gibbin, Emma M
Putnam, H M
Davy, Simon K
Gates, Ruth D
Adaptation of a globally important coccolithophore to ocean warming and acidification
topic_facet Acid-base regulation
Alkalinity
total
standard error
Animalia
Aragonite saturation state
Benthic animals
Benthos
Bicarbonate ion
Calcite saturation state
Calculated using seacarb after Nisumaa et al. (2010)
Carbon
inorganic
dissolved
Carbonate ion
Carbonate system computation flag
Carbon dioxide
Cnidaria
Coast and continental shelf
Containers and aquaria (20-1000 L or < 1 m**2)
Figure
Fugacity of carbon dioxide (water) at sea surface temperature (wet air)
Laboratory experiment
North Pacific
OA-ICC
Ocean Acidification International Coordination Centre
Partial pressure of carbon dioxide (water) at sea surface temperature (wet air)
pH
extracellular
intracellular
pH change
Pocillopora damicornis
Replicate
Salinity
Single species
Species
Temperature
water
Time in minutes
description Regulating intracellular pH (pHi) is critical for optimising the metabolic activity of corals, yet mechanisms involved in pH regulation and the buffering capacity within coral cells are not well understood. Our study investigated how the presence of symbiotic dinoflagellates affects the response of pHi to pCO2-driven seawater acidification in cells isolated from Pocillopora damicornis. Using the fluorescent dye BCECF-AM, in conjunction with confocal microscopy, we simultaneously characterised the response of pHi in host coral cells and their dinoflagellate symbionts, in symbiotic and non-symbiotic states under saturating light, with and without the photosynthetic inhibitor DCMU. Each treatment was run under control (pH 7.8) and CO2 acidified seawater conditions (decreasing pH from 7.8 - 6.8). After two hours of CO2 addition, by which time the external pH (pHe) had declined to 6.8, the dinoflagellate symbionts had increased their pHi by 0.5 pH units above control levels. In contrast, in both symbiotic and non-symbiotic host coral cells, 15 min of CO2 addition (0.2 pH unit drop in pHe) led to cytoplasmic acidosis equivalent to 0.4 pH units. Despite further seawater acidification over the duration of the experiment, the pHi of non-symbiotic coral cells did not change, though in host cells containing a symbiont cell the pHi recovered to control levels. This recovery was negated when cells were incubated with DCMU. Our results reveal that photosynthetic activity of the endosymbiont is tightly coupled with the ability of the host cell to recover from cellular acidosis after exposure to high CO2 / low pH.
format Dataset
author Gibbin, Emma M
Putnam, H M
Davy, Simon K
Gates, Ruth D
author_facet Gibbin, Emma M
Putnam, H M
Davy, Simon K
Gates, Ruth D
author_sort Gibbin, Emma M
title Adaptation of a globally important coccolithophore to ocean warming and acidification
title_short Adaptation of a globally important coccolithophore to ocean warming and acidification
title_full Adaptation of a globally important coccolithophore to ocean warming and acidification
title_fullStr Adaptation of a globally important coccolithophore to ocean warming and acidification
title_full_unstemmed Adaptation of a globally important coccolithophore to ocean warming and acidification
title_sort adaptation of a globally important coccolithophore to ocean warming and acidification
publisher PANGAEA
publishDate 2014
url https://doi.pangaea.de/10.1594/PANGAEA.837880
https://doi.org/10.1594/PANGAEA.837880
geographic Pacific
geographic_facet Pacific
genre Ocean acidification
genre_facet Ocean acidification
op_source Supplement to: Gibbin, Emma M; Putnam, H M; Davy, Simon K; Gates, Ruth D (2014): Intracellular pH and its response to CO2-driven seawater acidification in symbiotic versus non-symbiotic coral cells. Journal of Experimental Biology, 217(11), 1963-1969, https://doi.org/10.1242/jeb.099549
op_relation Lavigne, Héloïse; Epitalon, Jean-Marie; Gattuso, Jean-Pierre (2014): seacarb: seawater carbonate chemistry with R. R package version 3.0. https://cran.r-project.org/package=seacarb
https://doi.pangaea.de/10.1594/PANGAEA.837880
https://doi.org/10.1594/PANGAEA.837880
op_rights CC-BY-3.0: Creative Commons Attribution 3.0 Unported
Access constraints: unrestricted
info:eu-repo/semantics/openAccess
op_rightsnorm CC-BY
op_doi https://doi.org/10.1594/PANGAEA.837880
https://doi.org/10.1242/jeb.099549
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