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Venn, Alexander A; Tambutté, Eric; Steeve, Comeau; Tambutté, Sylvie (2022): Proton gradients across the coral calcifying cell layer: effects of light, ocean acidification and carbonate chemistry [dataset]. PANGAEA, https://doi.org/10.1594/PANGAEA.949400

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Abstract:
Internal pH measurements made in the extracellular calcifying medium (ECM), calcifying (calicoblastic) epithelium and mesoglea of the coral Stylophora pistillata using the fluorescent dye SNARF-1 and confocal microscopy. The measurements were made in light and darkness three experiments. Experiment 1 involved using coral samples maintained at pH 8 seawater. Experiment 2 involved placing samples in 4 seawater acidification conditions: pH 8, 7.8, 7.4 and 7.2 for 1 week. Experiment 3 involved placing samples in 4 levels of dissolved inorganic carbon concentration: elevated; ambient, low and very low for one week. The research was carried out at the Centre Scientifique de Monaco between 2014-2017. The aim of the experiment was to determine the pH gradient across the calcifying cell layer and determine how it responded to the three experiments.
Keyword(s):
biomineralization; Climate change; Laboratory experiment; pH regulation; physiology; scleractinians
Related to:
Venn, Alexander A; Tambutté, Eric; Comeau, Steeve; Tambutté, Sylvie (2022): Proton gradients across the coral calcifying cell layer: Effects of light, ocean acidification and carbonate chemistry. Frontiers in Marine Science, 9, 973908, https://doi.org/10.3389/fmars.2022.973908
Event(s):
Laboratory-experiments * Method/Device: Experiment (EXP)
Comment:
The experiments were done in the lab on coral samples that have been held in culture in Monaco for the last 30 years. The data file contains pH data from 3 experiments. In experiment 1corals were kept at seawater pH 8. In experiment 2. Corals were exposed to seawater acidification. In experiment 3 corals were exposed to manipulated DIC concentrations. The data are pH measurements taken from 3 internal compartments of the coral Stylophora pistillata: the mesoglea, the calcifying cells and the ECM.
Parameter(s):
#NameShort NameUnitPrincipal InvestigatorMethod/DeviceComment
1ExperimentExpVenn, Alexander A
2Experiment/study setupSetupVenn, Alexander A
3Species, unique identificationSpecies UIDVenn, Alexander A
4Species, unique identification (URI)Species UID (URI)Venn, Alexander A
5Species, unique identification (Semantic URI)Species UID (Semantic URI)Venn, Alexander A
6CommentCommentVenn, Alexander AFigure
7TreatmentTreatVenn, Alexander A
8Temperature, waterTemp°CVenn, Alexander AThermometer
9SalinitySalVenn, Alexander A
10pHpHVenn, Alexander AConfocal Microscope, Leica, SP5Light
11pH, standard deviationpH std dev±Venn, Alexander AConfocal Microscope, Leica, SP5Light
12pHpHVenn, Alexander AConfocal Microscope, Leica, SP5Dark
13pH, standard deviationpH std dev±Venn, Alexander AConfocal Microscope, Leica, SP5Dark
14pH, extracellularpHeVenn, Alexander AConfocal Microscope, Leica, SP5Light
15pH, extracellular, standard deviationpHe std dev±Venn, Alexander AConfocal Microscope, Leica, SP5Light
16pH, extracellularpHeVenn, Alexander AConfocal Microscope, Leica, SP5Dark
17pH, extracellular, standard deviationpHe std dev±Venn, Alexander AConfocal Microscope, Leica, SP5Dark
18pH, intracellularpH inVenn, Alexander AConfocal Microscope, Leica, SP5Light
19pH, intracellular, standard deviationpH in std dev±Venn, Alexander AConfocal Microscope, Leica, SP5Light
20pH, intracellularpH inVenn, Alexander AConfocal Microscope, Leica, SP5Dark
21pH, intracellular, standard deviationpH in std dev±Venn, Alexander AConfocal Microscope, Leica, SP5Dark
22pH, mesogleaph mgVenn, Alexander AConfocal Microscope, Leica, SP5Light
23pH, mesoglea, standard deviationpH mg std dev±Venn, Alexander AConfocal Microscope, Leica, SP5Light
24pH, mesogleaph mgVenn, Alexander AConfocal Microscope, Leica, SP5Dark
25pH, mesoglea, standard deviationpH mg std dev±Venn, Alexander AConfocal Microscope, Leica, SP5Dark
Status:
Curation Level: Enhanced curation (CurationLevelC)
Size:
201 data points

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