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    PANGAEA
    In:  Supplement to: McCarthy, Avery; Rogers, Susan P; Duffy, Stephen J; Campbell, Douglas A (2012): Elevated carbon dioxide differentially alters the photophysiology of Thalassiosira pseudonana (Bacillariophyceae) and Emiliania huxleyi (Haptophyta). Journal of Phycology, 48(3), 635-646, https://doi.org/10.1111/j.1529-8817.2012.01171.x
    Publication Date: 2024-03-18
    Description: Increasing anthropogenic carbon dioxide is causing changes to ocean chemistry, which will continue in a predictable manner. Dissolution of additional atmospheric carbon dioxide leads to increased concentrations of dissolved carbon dioxide and bicarbonate and decreased pH in ocean water. The concomitant effects on phytoplankton ecophysiology, leading potentially to changes in community structure, are now a focus of concern. Therefore, we grew the coccolithophore Emiliania huxleyi (Lohmann) W. W. Hay et H. Mohler and the diatom strains Thalassiosira pseudonana (Hust.) Hasle et Heimdal CCMP 1014 and T. pseudonana CCMP 1335 under low light in turbidostat photobioreactors bubbled with air containing 390 ppmv or 750 ppmv CO2. Increased pCO2 led to increased growth rates in all three strains. In addition, protein levels of RUBISCO increased in the coastal strains of both species, showing a larger capacity for CO2 assimilation at 750 ppmv CO2. With increased pCO2, both T. pseudonana strains displayed an increased susceptibility to PSII photoinactivation and, to compensate, an augmented capacity for PSII repair. Consequently, the cost of maintaining PSII function for the diatoms increased at increased pCO2. In E. huxleyi, PSII photoinactivation and the counter-acting repair, while both intrinsically larger than in T. pseudonana, did not change between the current and high-pCO2 treatments. The content of the photosynthetic electron transport intermediary cytochrome b6/f complex increased significantly in the diatoms under elevated pCO2, suggesting changes in electron transport function.
    Keywords: Alkalinity, total; Aragonite saturation state; Bicarbonate ion; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, organic, particulate, per cell; Carbon/Nitrogen ratio; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Cell biovolume; Cell density; CF1 subunit of ATP synthase protein; Chlorophyll a; Chlorophyll c1/chlorophyll a ratio; Chlorophyll c2/chlorophyll a ratio; Chlorophyll c3/chlorophyll a ratio; Chromista; Cytochrome c1; Diadinoxanthin/chlorophyll a ratio; Diatoxanthin/chlorophyll a ratio; Effective absorbance cross-section of photosystem II; Emiliania huxleyi; Fucoxanthin/chlorophyll a ratio; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Haptophyta; Identification; Irradiance; Laboratory experiment; Laboratory strains; Non photochemical quenching; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Ochrophyta; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; Phosphate; Photochemical quenching; Photosynthetic protein, PsbC; Photosynthetic protein PsbA; Photosynthetic protein PsbD; Photosynthetic protein Rubisco; Phytoplankton; Potentiometric; Primary production/Photosynthesis; Protein per cell; Replicates; Salinity; Silicate; Single species; Species; Strain; Temperature, water; Thalassiosira pseudonana; Time in minutes; Treatment
    Type: Dataset
    Format: text/tab-separated-values, 1086 data points
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