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  • 1
    Publication Date: 2012-09-05
    Print ISSN: 1438-387X
    Electronic ISSN: 1438-3888
    Topics: Biology
    Published by BioMed Central
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  • 2
  • 3
    Publication Date: 2013-05-01
    Print ISSN: 0024-3590
    Electronic ISSN: 1939-5590
    Topics: Biology , Geosciences , Physics
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  • 4
    facet.materialart.
    Unknown
    Elsevier
    In:  Journal of Experimental Marine Biology and Ecology, 413 . pp. 131-137.
    Publication Date: 2020-07-24
    Description: The coccolithophore Calcidiscus leptoporus was grown in batch culture under nitrogen (N) as well as phosphorus (P) limitation. Growth rate, particulate inorganic carbon (PIC), particulate organic carbon (POC), particulate organic nitrogen (PON), and particulate organic phosphorus (POP) production were determined and coccolith morphology was analysed. While PON production decreased by 70% under N-limitation and POP production decreased by 65% under P-limitation, growth rate decreased by 33% under N- as well as P-limitation. POC as well as PIC production (calcification rate) increased by 27% relative to the control under P-limitation, and did not change under N-limitation. Coccolith morphology did not change in response to either P or N limitation. While these findings, supported by a literature survey, suggest that coccolith morphogenesis is not hampered by either P or N limitation, calcification rate might be. The latter conclusion is in apparent contradiction to our data. We discuss the reasons for this inference
    Type: Article , PeerReviewed
    Format: text
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  • 5
    Publication Date: 2023-12-12
    Description: Near-daily concentrations of Chlorophyll a and phaeopigments from RV Polarsterns underway water supply system (inlet at 11m water depth) collected during legs 1,3,4, and 5 of the MOSAiC (PS122) drift expedition in the central Arctic Ocean. 2-4L of water were filtered onto pre-combusted GF/F filters (nominal pore size 0.7µm) and frozen at -80°C. Samples were subsequently extracted in 90°C acetone, homogenized using a cell mill, and measured on the following day using a Turner flourometer, followed by an acidification step to determine phaeopigments (see Knap et al. 1996 for details and calculations). Samples were collected from end of October 2019 to beginning of October 2020, with a gap between mid-December and the end of February.
    Keywords: Acidification method according to Knap et al. (1996); Activity description; Arctic Ocean; Cast number; CHLa; Chl-a; Chlorophyll a; DATE/TIME; DEPTH, water; Device type; Event label; LATITUDE; Leg Number; LONGITUDE; Mosaic; MOSAiC; MOSAiC_ECO; MOSAiC20192020; Multidisciplinary drifting Observatory for the Study of Arctic Climate; North Greenland Sea; Phaeopigments; pigments; Pigments, Turner fluorometer; Polarstern; PS122/1; PS122/1_10-109; PS122/1_10-84; PS122/1_10-85; PS122/1_10-86; PS122/1_10-87; PS122/1_10-88; PS122/1_10-89; PS122/1_11-14; PS122/1_11-2; PS122/1_11-26; PS122/1_11-36; PS122/1_11-48; PS122/1_5-42; PS122/1_5-44; PS122/1_5-87; PS122/1_6-88; PS122/1_6-89; PS122/1_6-90; PS122/1_6-91; PS122/1_6-92; PS122/1_6-94; PS122/1_7-115; PS122/1_7-116; PS122/1_7-117; PS122/1_7-118; PS122/1_7-119; PS122/1_7-132; PS122/1_8-127; PS122/1_8-89; PS122/1_8-90; PS122/1_8-91; PS122/1_8-92; PS122/1_8-93; PS122/1_9-112; PS122/1_9-82; PS122/1_9-83; PS122/1_9-84; PS122/1_9-85; PS122/1_9-86; PS122/3; PS122/3_29-78; PS122/3_29-89; PS122/3_30-15; PS122/3_30-49; PS122/3_30-51; PS122/3_30-63; PS122/3_30-80; PS122/3_30-93; PS122/3_31-14; PS122/3_31-27; PS122/3_31-40; PS122/3_31-48; PS122/3_31-58; PS122/3_31-74; PS122/3_31-83; PS122/3_32-20; PS122/3_32-35; PS122/3_32-4; PS122/3_32-47; PS122/3_32-49; PS122/3_32-69; PS122/3_32-87; PS122/3_33-16; PS122/3_33-49; PS122/3_33-54; PS122/3_33-6; PS122/3_33-77; PS122/3_33-94; PS122/3_33-95; PS122/3_34-19; PS122/3_34-33; PS122/3_34-44; PS122/3_34-48; PS122/3_34-6; PS122/3_34-73; PS122/3_34-82; PS122/3_35-101; PS122/3_35-109; PS122/3_35-27; PS122/3_35-45; PS122/3_35-6; PS122/3_35-68; PS122/3_35-86; PS122/3_36-100; PS122/3_36-126; PS122/3_36-136; PS122/3_36-33; PS122/3_36-36; PS122/3_36-7; PS122/3_36-71; PS122/3_37-10; PS122/3_37-106; PS122/3_37-107; PS122/3_37-113; PS122/3_37-13; PS122/3_37-43; PS122/3_37-54; PS122/3_38-153; PS122/3_38-154; PS122/3_38-156; PS122/3_38-23; PS122/3_38-29; PS122/3_38-73; PS122/3_39-118; PS122/3_39-119; PS122/3_39-120; PS122/3_39-121; PS122/3_39-122; PS122/3_39-123; PS122/3_39-124; PS122/3_40-23; PS122/3_40-24; PS122/3_40-25; PS122/3_40-56; PS122/3_40-57; PS122/3_40-58; PS122/3_40-59; PS122/3_41-28; PS122/3_41-29; PS122/3_41-30; PS122/3_41-31; PS122/3_41-39; PS122/3_41-43; PS122/3_41-49; PS122/3_42-15; PS122/3_42-2; PS122/3_42-22; PS122/3_42-36; PS122/3_42-37; PS122/3_42-46; PS122/3_42-54; PS122/3_42-59; PS122/3_42-7; PS122/4; PS122/4_44-104; PS122/4_44-117; PS122/4_44-132; PS122/4_44-148; PS122/4_44-163; PS122/4_44-168; PS122/4_44-176; PS122/4_44-192; PS122/4_44-20; PS122/4_44-21; PS122/4_44-212; PS122/4_44-33; PS122/4_44-40; PS122/4_44-41; PS122/4_44-55; PS122/4_44-66; PS122/4_44-84; PS122/4_44-86; PS122/4_44-93; PS122/4_44-94; PS122/4_45-109; PS122/4_45-110; PS122/4_45-111; PS122/4_45-134; PS122/4_45-27; PS122/4_45-28; PS122/4_45-49; PS122/4_46-10; PS122/4_46-156; PS122/4_46-157; PS122/4_46-158; PS122/4_46-159; PS122/4_46-34; PS122/4_46-54; PS122/4_47-141; PS122/4_47-142; PS122/4_47-15; PS122/4_47-30; PS122/4_47-78; PS122/4_47-79; PS122/4_47-95; PS122/4_48-107; PS122/4_48-108; PS122/4_48-109; PS122/4_48-110; PS122/4_48-16; PS122/4_48-181; PS122/4_48-182; PS122/4_49-104; PS122/4_49-13; PS122/4_49-41; PS122/4_49-42; PS122/4_49-60; PS122/4_49-65; PS122/4_49-84; PS122/4_50-15; PS122/4_50-23; PS122/4_50-33; PS122/4_50-46; PS122/4_50-54; PS122/4_50-6; PS122/4_50-60; PS122/4_50-63; PS122/4_50-76; PS122/5; PS122/5_59-118; PS122/5_59-131; PS122/5_59-150; PS122/5_59-157; PS122/5_59-165; PS122/5_59-166; PS122/5_59-177; PS122/5_59-190; PS122/5_59-205; PS122/5_59-221; PS122/5_59-24; PS122/5_59-257; PS122/5_59-283; PS122/5_59-289; PS122/5_59-3; PS122/5_59-34; PS122/5_59-385; PS122/5_59-386; PS122/5_59-387; PS122/5_59-388; PS122/5_59-48; PS122/5_59-49; PS122/5_59-52; PS122/5_59-54; PS122/5_59-56; PS122/5_59-71; PS122/5_59-9; PS122/5_60-132; PS122/5_60-252; PS122/5_60-253; PS122/5_60-254; PS122/5_60-255; PS122/5_60-256; PS122/5_60-257; PS122/5_61-120; PS122/5_61-121; PS122/5_61-122; PS122/5_61-306; PS122/5_61-307; PS122/5_61-308; PS122/5_61-309; PS122/5_62-245; PS122/5_62-246; PS122/5_62-247; PS122/5_62-248; PS122/5_62-249; PS122/5_62-250; PS122/5_62-251; PS122/5_63-113; PS122/5_63-114; PS122/5_63-147; PS122/5_63-148; PS122/5_63-149; PS122/5_63-22; PS122/5_63-23; PS122/5_63-26; PS122/5_63-65; PS122/5_63-67; PS122/5_63-79; Tap; TAP; under ice; Underway water sampling; UWS; Volume
    Type: Dataset
    Format: text/tab-separated-values, 3863 data points
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  • 6
    Publication Date: 2023-12-12
    Description: Concentrations of Chlorophyll a and phaeopigments from CTD-rosette casts during the MOSAiC (PS122) drift expedition in the central Arctic Ocean. 2-4L of water were filtered onto precombusted GF/F filters (nominal pore size 0.7µm) and frozen at -80°C. Samples were subsequently extracted in 90°C acetone,homogenized using a cell mill, and meaured on the following day using a Turner flourometer, followed by an acidification step to determine pheopigments (see Knap et al. 1994 for details and calculations). Samples were collected roughly once per week from end of October 2019 to beginning of October 2020.
    Keywords: Acidification method according to Knap et al. (1996); Activity description; Arctic; Arctic Ocean; Cast number; Chl-a; Chlorophyll a; Collector; CTD/Rosette; CTD-RO; DATE/TIME; DEPTH, water; Device type; Event label; Feature; LATITUDE; Leg Number; LONGITUDE; MOSAiC; MOSAiC_ECO; MOSAiC20192020; Multidisciplinary drifting Observatory for the Study of Arctic Climate; phaeopigments; Phaeopigments; Phytoplankton; pigments; Pigments, Turner fluorometer; Polarstern; PS122/1; PS122/1_10-44; PS122/1_5-40; PS122/1_5-59; PS122/1_6-58; PS122/1_7-49; PS122/1_8-46; PS122/1_9-50; PS122/2; PS122/2_17-41; PS122/2_18-34; PS122/2_19-56; PS122/2_20-46; PS122/2_21-1; PS122/2_21-65; PS122/2_22-47; PS122/2_23-63; PS122/2_24-4; PS122/2_25-54; PS122/3; PS122/3_30-41; PS122/3_30-53; PS122/3_31-39; PS122/3_31-59; PS122/3_32-75; PS122/3_33-69; PS122/3_34-65; PS122/3_34-66; PS122/3_34-77; PS122/3_35-63; PS122/3_36-81; PS122/3_37-45; PS122/3_38-54; PS122/3_39-51; PS122/3_40-36; PS122/4; PS122/4_44-184; PS122/4_44-67; PS122/4_45-100; PS122/4_45-31; PS122/4_45-75; PS122/4_45-79; PS122/4_45-82; PS122/4_45-85; PS122/4_45-96; PS122/4_46-60; PS122/4_47-52; PS122/4_48-62; PS122/4_49-25; PS122/5; PS122/5_59-274; PS122/5_59-306; PS122/5_59-357; PS122/5_59-72; PS122/5_60-69; PS122/5_60-89; PS122/5_61-161; PS122/5_62-91; PS122/5_63-53; Sample code/label
    Type: Dataset
    Format: text/tab-separated-values, 2273 data points
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  • 7
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Trimborn, Scarlett; Thoms, Silke; Brenneis, Tina; Heiden, Jasmin; Beszteri, Sara; Bischof, Kai (2017): Two Southern Ocean diatoms are more sensitive to ocean acidification and changes in irradiance than the prymnesiophyte Phaeocystis antarctica. Physiologia Plantarum, https://doi.org/10.1111/ppl.12539
    Publication Date: 2024-03-15
    Description: To better understand the impact of ocean acidification (OA) and changes in light availability on Southern Ocean phytoplankton physiology, we investigated the effects of pCO2 (380 and 800 µatm) in combination with low and high irradiance (20 or 50 and 200 µmol photons/m2/s) on growth, particulate organic carbon (POC) fixation and photophysiology in the three ecologically relevant species Chaetoceros debilis, Fragilariopsis kerguelensis and Phaeocystis antarctica. Irrespective of the light scenario, neither growth nor POC per cell was stimulated by OA in any of the tested species and the two diatoms even displayed negative responses in growth (e.g. C. debilis) or POC content (e.g. F. kerguelensis) under OA in conjunction with high light. For both diatoms, also maximum quantum yields of PSII (Fv/Fm) were decreased under these conditions, indicating lowered photochemical efficiencies. To counteract the negative effects by OA and high light, the two diatoms showed diverging photoacclimation strategies. While cellular chlorophyll a and fucoxanthin contents were enhanced in C. debilis to potentially maximize light absorption, F. kerguelensis exhibited reduced chlorophyll a per cell, increased disconnection of antennae from photosystem II reaction centers and strongly lowered absolute electron transport rates (ETR). The decline in ETRs in F. kerguelensis might be explained in terms of different species-specific strategies for tuning the available flux of adenosine triphosphate and nicotinamide adenine dinucleotide phosphate. Overall, our results revealed that P. antarctica was more tolerant to OA and changes in irradiance than the two diatoms, which may have important implications for biogeochemical cycling.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Antarctic; Aragonite saturation state; Bicarbonate ion; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbon, organic, particulate, per cell; Carbon, organic, particulate, standard deviation; Carbon/Nitrogen ratio; Carbon/Nitrogen ratio, standard deviation; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Chaetoceros debilis; Chromista; Electron transport rate; Electron transport rate, standard deviation; Fragilariopsis kerguelensis; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Growth rate, standard deviation; Haptophyta; Irradiance; Laboratory experiment; Maximum photochemical quantum yield of photosystem II; Maximum photochemical quantum yield of photosystem II, standard deviation; Non photochemical quenching; Non photochemical quenching, standard deviation; OA-ICC; Ocean Acidification International Coordination Centre; Ochrophyta; Open ocean; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; pH, standard deviation; Phaeocystis antarctica; Phytoplankton; Polar; Primary production/Photosynthesis; Registration number of species; Salinity; Single species; Species; Temperature, water; Treatment; Type; Uniform resource locator/link to reference; Yield; Yield, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 7396 data points
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  • 8
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Langer, Gerald; Oetjen, Kerstin; Brenneis, Tina (2012): Calcification of Calcidiscus leptoporus under nitrogen and phosphorus limitation. Journal of Experimental Marine Biology and Ecology, 413, 131-137, https://doi.org/10.1016/j.jembe.2011.11.028
    Publication Date: 2024-03-15
    Description: The coccolithophore Calcidiscus leptoporus was grown in batch culture under nitrogen (N) as well as phosphorus (P) limitation. Growth rate, particulate inorganic carbon (PIC), particulate organic carbon (POC), particulate organic nitrogen (PON), and particulate organic phosphorus (POP) production were determined and coccolith morphology was analysed. While PON production decreased by 70% under N-limitation and POP production decreased by 65% under P-limitation, growth rate decreased by 33% under N- as well as P-limitation. POC as well as PIC production (calcification rate) increased by 27% relative to the control under P-limitation, and did not change under N-limitation. Coccolith morphology did not change in response to either P or N limitation. While these findings, supported by a literature survey, suggest that coccolith morphogenesis is not hampered by either P or N limitation, calcification rate might be. The latter conclusion is in apparent contradiction to our data. We discuss the reasons for this inference.
    Keywords: AA; Alkalinity, Gran titration (Gran, 1950); Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Autoanalyzer; Bicarbonate ion; BIOACID; Biological Impacts of Ocean Acidification; Biomass/Abundance/Elemental composition; Bottles or small containers/Aquaria (〈20 L); Calcidiscus leptoporus; Calcidiscus leptoporus, standard deviation; Calcification/Dissolution; Calcification rate, standard deviation; Calcification rate of carbon per cell; Calcite saturation state; Calculated, see reference(s); Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbon, inorganic, particulate, per cell; Carbon, organic, particulate, per cell; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Chromista; Element analyser CNS, EURO EA; EPOCA; EUR-OCEANS; European network of excellence for Ocean Ecosystems Analysis; European Project on Ocean Acidification; Experimental treatment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Growth rate, standard deviation; Haptophyta; Laboratory experiment; Laboratory strains; Light:Dark cycle; Macro-nutrients; Measured; Mediterranean Sea Acidification in a Changing Climate; MedSeA; Nitrate; Nitrate, standard deviation; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Particulate inorganic carbon per cell, standard deviation; Particulate organic carbon, production, standard deviation; Particulate organic carbon content per cell, standard deviation; Particulate organic carbon production per cell; Particulate organic nitrogen per cell; Particulate organic nitrogen per cell, standard deviation; Particulate organic nitrogen production, standard deviation; Particulate organic phosphorus per cell; Particulate organic phosphorus per cell, standard deviation; Particulate organic phosphorus production; Particulate organic phosphorus production per cell; Pelagos; pH; pH, standard deviation; pH meter, WTW, 340i; Phosphate; Phosphate, standard deviation; Phytoplankton; Primary production/Photosynthesis; Production of particulate organic nitrogen; Radiation, photosynthetically active; Salinity; Sample ID; Seal QuAAtro SFA Analyzer, Seal Analytical, 800 TM; Single species; South Atlantic; Species; Temperature, water; Tetra Con 325 salinity and temperature probe
    Type: Dataset
    Format: text/tab-separated-values, 238 data points
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  • 9
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Trimborn, Scarlett; Brenneis, Tina; Hoppe, Clara Jule Marie; Laglera, Luis Miguel; Norman, Louiza; Santos-Echeandía, Juan; Völkner, Christian; Wolf-Gladrow, Dieter A; Hassler, Christel S (2017): Iron sources alter the response of Southern Ocean phytoplankton to ocean acidification. Marine Ecology Progress Series, 578, 35-50, https://doi.org/10.3354/meps12250
    Publication Date: 2024-03-15
    Description: The rise in anthropogenic CO2 and the associated ocean acidification (OA) will change trace metal solubility and speciation, potentially altering Southern Ocean (SO) phytoplankton productivity and species composition. As iron (Fe) sources are important determinants of Fe bioavailability, we assessed the effect of Fe-laden dust versus inorganic Fe (FeCl3) enrichment under ambient and high pCO2 levels (390 and 900 μatm) in a naturally Fe-limited SO phytoplankton community. Despite similar Fe chemical speciation and net particulate organic carbon (POC) production rates, CO2-dependent species shifts were controlled by Fe sources. Final phytoplankton communities of both control and dust treatments were dominated by the same species, with an OA-dependent shift from the diatom Pseudo nitzschia prolongatoides towards the prymnesiophyte Phaeocystis antarctica. Addition of FeCl3 resulted in high abundances of Nitzschia lecointei and Chaetoceros neogracilis under ambient and high pCO2, respectively. These findings reveal that both the characterization of the phytoplankton community at the species level and the use of natural Fe sources are essential for a realistic projection of the biological carbon pump in the Fe-limited pelagic SO under OA. As dust deposition represents a more realistic scenario for the Fe-limited pelagic SO under OA, unaffected net POC production and dominance of P. antarctica can potentially weaken the export of carbon and silica in the future.
    Keywords: Abundance; Abundance, standard deviation; Alkalinity, total; Alkalinity, total, standard deviation; Antarctic; Aragonite saturation state; Bicarbonate ion; Biogenic particulate silica/Carbon, organic, particulate; Biogenic particulate silica/Carbon, organic, particulate, standard deviation; Biomass/Abundance/Elemental composition; 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, inorganic, dissolved, standard deviation; Carbon, organic, particulate, net production; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Cell density; Cell density, standard deviation; Community composition and diversity; Entire community; EXP; Experiment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth rate; Growth rate, standard deviation; Iron, chemically labile; Iron, dissolved; Iron, dissolved, inorganic; Iron, dissolved, standard deviation; Iron, inorganic, conditional stability constants; Iron, inorganic, conditional stability constants, standard deviation; Iron uptake/Carbon, organic, particulate; Iron uptake/Carbon, organic, particulate, standard deviation; Laboratory experiment; Ligand concentration; Ligand concentration, standard deviation; Maximum photochemical quantum yield of photosystem II; Maximum photochemical quantum yield of photosystem II, standard deviation; Micro-nutrients; Nitrate; Nitrate, standard deviation; OA-ICC; Ocean Acidification International Coordination Centre; Open ocean; Other metabolic rates; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Particulate inorganic carbon per cell; Pelagos; pH; pH, standard deviation; Polar; Polar_front; Primary production/Photosynthesis; Salinity; Side coefficient of dissolved Fe-complex ligands; Temperature, water; Time in days; Time point, descriptive; Treatment; Type
    Type: Dataset
    Format: text/tab-separated-values, 4906 data points
    Location Call Number Expected Availability
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  • 10
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Trimborn, Scarlett; Brenneis, Tina; Sweet, Elizabeth; Rost, Björn (2013): Sensitivity of Antarctic phytoplankton species to ocean acidification: Growth, carbon acquisition, and species interaction. Limnology and Oceanography, 58(3), 997-1007, https://doi.org/10.4319/lo.2013.58.3.0997
    Publication Date: 2024-03-15
    Description: Despite the fact that ocean acidification is considered to be especially pronounced in the Southern Ocean, little is known about CO2-dependent physiological processes and the interactions of Antarctic phytoplankton key species. We therefore studied the effects of CO2 partial pressure (PCO2) (16.2, 39.5, and 101.3 Pa) on growth and photosynthetic carbon acquisition in the bloom-forming species Chaetoceros debilis, Pseudo-nitzschia subcurvata, Fragilariopsis kerguelensis, and Phaeocystis antarctica. Using membrane-inlet mass spectrometry, photosynthetic O2 evolution and inorganic carbon (Ci) fluxes were determined as a function of CO2 concentration. Only the growth of C. debilis was enhanced under high PCO2. Analysis of the carbon concentrating mechanism (CCM) revealed the operation of very efficient CCMs (i.e., high Ci affinities) in all species, but there were species-specific differences in CO2-dependent regulation of individual CCM components (i.e., CO2 and uptake kinetics, carbonic anhydrase activities). Gross CO2 uptake rates appear to increase with the cell surface area to volume ratios. Species competition experiments with C. debilis and P. subcurvata under different PCO2 levels confirmed the CO2-stimulated growth of C. debilis observed in monospecific incubations, also in the presence of P. subcurvata. Independent of PCO2, high initial cell abundances of P. subcurvata led to reduced growth rates of C. debilis. For a better understanding of future changes in phytoplankton communities, CO2-sensitive physiological processes need to be identified, but also species interactions must be taken into account because their interplay determines the success of a species.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Antarctic; Aragonite saturation state; Bicarbonate ion; Bicarbonate ion, reciprocal of photosynthetic affinity value; Bicarbonate ion, reciprocal of photosynthetic affinity value, standard deviation; Bicarbonate uptake/net fixation ratio; Bicarbonate uptake/net fixation ratio, standard deviation; Bicarbonate uptake per chlorophyll a, maximum velocity, standard deviation; Bicarbonate uptake rate, per chlorophyll a, maximum velocity; 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, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, reciprocal of photosynthetic affinity value; Carbon dioxide, reciprocal of photosynthetic affinity value, standard deviation; Carbon dioxide, standard deviation; Cell surface area/cell volume, standard deviation; Cell surface area/cell volume ratio; Chaetoceros debilis; Chaetoceros debilis/Pseudo-nitzschia subcurvata ratio; Chaetoceros debilis/Pseudo-nitzschia subcurvata ratio, standard deviation; Chromista; Description; Extracellular carbonic anhydrase activity; Extracellular carbonic anhydrase activity, standard deviation; Fragilariopsis kerguelensis; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Gross carbon dioxide uptake, half saturation concentration; Gross carbon dioxide uptake, half saturation concentration, standard deviation; Gross carbon dioxide uptake/net fixation ratio; Gross carbon dioxide uptake/net fixation ratio, standard deviation; Gross carbon dioxide uptake per chlorophyll a, maximum velocity, standard deviation; Gross carbon dioxide uptake rate, per chlorophyll a, maximum velocity; Growth/Morphology; Growth rate; Growth rate, standard deviation; Identification; Laboratory experiment; Laboratory strains; Measured by loss of 18O (Silverman, 1982); Net carbon dioxide uptake, half saturation concentration; Net carbon dioxide uptake, half saturation concentration, standard deviation; Net carbon dioxide uptake per chlorophyll a, maximum velocity, standard deviation; Net carbon dioxide uptake rate, per chlorophyll a, maximum velocity; Nitrate; OA-ICC; Ocean Acidification International Coordination Centre; Ochrophyta; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; pH, standard deviation; Phaeocystis antarctica; Phosphate; Photosynthesis carbon dioxide uptake, maximum velocity, standard deviation; Photosynthesis carbon dioxide uptake rate, maximum velocity; Phytoplankton; Potentiometric; Potentiometric titration; Primary production/Photosynthesis; Priority Programme 1158 Antarctic Research with Comparable Investigations in Arctic Sea Ice Areas; Pseudo-nitzschia subcurvata; Salinity; Silicate; Single species; Species; Species interaction; SPP1158; Temperature, water; Treatment
    Type: Dataset
    Format: text/tab-separated-values, 1753 data points
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