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  • BIOACID; Biological Impacts of Ocean Acidification  (2)
  • Abundance per volume; Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Bicarbonate ion; BIOACID; Biological Impacts of Ocean Acidification; Biomass/Abundance/Elemental composition; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calcite saturation state, standard deviation; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, particulate, per cell; Carbon, organic, dissolved, per cell; Carbon, organic, dissolved/Nitrogen, organic, dissolved ratio; Carbon, organic, particulate, per cell; Carbon, organic, particulate, standard deviation; Carbon, organic, particulate/Nitrogen, particulate ratio; Carbon, organic, particulate/Nitrogen, particulate ratio, standard deviation; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, partial pressure; Chlorophyll a, standard deviation; Chlorophyll a per cell; Chromista; Day of experiment; Emiliania huxleyi; Emiliania huxleyi, standard deviation; Figure; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Haptophyta; Laboratory experiment; Laboratory strains; Nitrogen, organic, dissolved, per cell; Nitrogen, particulate, per cell; Nitrogen, total, particulate/Phosphorus, organic, particulate, ratio; Nitrogen, total, particulate/Phosphorus, organic, particulate, ratio, standard deviation; Not applicable; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Particulate inorganic carbon/particulate organic carbon ratio; Particulate inorganic carbon/particulate organic carbon ratio, standard deviation; Pelagos; pH; pH, standard deviation; Phosphorus, organic, particulate, per cell; Phytoplankton; Salinity; Single species; Species; Standard deviation; Temperature, water  (1)
  • 2010-2014  (3)
Document type
Keywords
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  • 2010-2014  (3)
Year
  • 1
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    PANGAEA
    In:  Supplement to: Wannicke, Nicola; Endres, Sonja; Engel, Anja; Grossart, Hans-Peter; Unger, Juliane; Voss, Maren (2012): Response of Nodularia spumigena to pCO2 - Part 1: Growth, production and nitrogen cycling. Biogeosciences, 9(8), 2973-2988, https://doi.org/10.5194/bg-9-2973-2012
    Publication Date: 2023-05-12
    Description: Heterocystous cyanobacteria of the genus Nodularia form extensive blooms in the Baltic Sea and contribute substantially to the total annual primary production. Moreover, they dispense a large fraction of new nitrogen to the ecosystem when inorganic nitrogen concentration in summer is low. Thus, it is of ecological importance to know how Nodularia will react to future environmental changes, in particular to increasing carbon dioxide (CO2) concentrations and what consequences there might arise for cycling of organic matter in the Baltic Sea. Here, we determined carbon (C) and dinitrogen (N2) fixation rates, growth, elemental stoichiometry of particulate organic matter and nitrogen turnover in batch cultures of the heterocystous cyanobacterium Nodularia spumigena under low (median 315 µatm), mid (median 353 µatm), and high (median 548 µatm) CO2 concentrations. Our results demonstrate an overall stimulating effect of rising pCO2 on C and N2 fixation, as well as on cell growth. An increase in pCO2 during incubation days 0 to 9 resulted in an elevation in growth rate by 84 ± 38% (low vs. high pCO2) and 40 ± 25% (mid vs. high pCO2), as well as in N2 fixation by 93 ± 35% and 38 ± 1%, respectively. C uptake rates showed high standard deviations within treatments and in between sampling days. Nevertheless, C fixation in the high pCO2 treatment was elevated compared to the other two treatments by 97% (high vs. low) and 44% (high vs. mid) at day 0 and day 3, but this effect diminished afterwards. Additionally, elevation in carbon to nitrogen and nitrogen to phosphorus ratios of the particulate biomass formed (POC : POP and PON : POP) was observed at high pCO2. Our findings suggest that rising pCO2 stimulates the growth of heterocystous diazotrophic cyanobacteria, in a similar way as reported for the non-heterocystous diazotroph Trichodesmium. Implications for biogeochemical cycling and food web dynamics, as well as ecological and socio-economical aspects in the Baltic Sea are discussed.
    Keywords: BIOACID; Biological Impacts of Ocean Acidification
    Type: Dataset
    Format: application/zip, 3 datasets
    Location Call Number Limitation Availability
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  • 2
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    PANGAEA
    In:  Supplement to: Schulz, Kai Georg; Bellerby, Richard G J; Brussaard, Corina P D; Büdenbender, Jan; Czerny, Jan; Engel, Anja; Fischer, Matthias; Krug, Sebastian; Lischka, Silke; Koch-Klavsen, Stephanie; Ludwig, Andrea; Meyerhöfer, Michael; Nondal, G; Silyakova, Anna; Stuhr, Annegret; Riebesell, Ulf (2013): Temporal biomass dynamics of an Arctic plankton bloom in response to increasing levels of atmospheric carbon dioxide. Biogeosciences, 10(1), 161-180, https://doi.org/10.5194/bg-10-161-2013
    Publication Date: 2023-10-21
    Description: Ocean acidification and carbonation, driven by anthropogenic emissions of carbon dioxide (CO2), have been shown to affect a variety of marine organisms and are likely to change ecosystem functioning. High latitudes, especially the Arctic, will be the first to encounter profound changes in carbonate chemistry speciation at a large scale, namely the under-saturation of surface waters with respect to aragonite, a calcium carbonate polymorph produced by several organisms in this region. During a CO2 perturbation study in 2010, in the framework of the EU-funded project EPOCA, the temporal dynamics of a plankton bloom was followed in nine mesocosms, manipulated for CO2 levels ranging initially from about 185 to 1420 matm. Dissolved inorganic nutrients were added halfway through the experiment. Autotrophic biomass, as identified by chlorophyll a standing stocks (Chl a), peaked three times in all mesocosms. However, while absolute Chl a concentrations were similar in all mesocosms during the first phase of the experiment, higher autotrophic biomass was measured at high in comparison to low CO2 during the second phase, right after dissolved inorganic nutrient addition. This trend then reversed in the third phase. There were several statistically significant CO2 effects on a variety of parameters measured in certain phases, such as nutrient utilization, standing stocks of particulate organic matter, and phytoplankton species composition. Interestingly, CO2 effects developed slowly but steadily, becoming more and more statistically significant with time. The observed CO2 related shifts in nutrient flow into different phytoplankton groups (mainly diatoms, dinoflagellates, prasinophytes and haptophytes) could have consequences for future organic matter flow to higher trophic levels and export production, with consequences for ecosystem productivity and atmospheric CO2.
    Keywords: BIOACID; Biological Impacts of Ocean Acidification
    Type: Dataset
    Format: application/zip, 2 datasets
    Location Call Number Limitation Availability
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  • 3
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    PANGAEA
    In:  Supplement to: Engel, Anja; Cisternas Novoa, Carolina; Wurst, Mascha; Endres, Sonja; Tang, Tiantian; Schartau, Markus; Lee, Cindy (2014): No detectable effect of CO2 on elemental stoichiometry of Emiliania huxleyi in nutrient-limited, acclimated continuous cultures. Marine Ecology Progress Series, 507, 15-30, https://doi.org/10.3354/meps10824
    Publication Date: 2024-04-27
    Description: Effects of CO2 concentration on elemental composition of the coccolithophore Emiliania huxleyi were studied in phosphorus-limited, continuous cultures that were acclimated to experimental conditions for 30 d prior to the first sampling. We determined phytoplankton and bacterial cell numbers, nutrients, particulate components like organic carbon (POC), inorganic carbon (PIC), nitrogen (PN), organic phosphorus (POP), transparent exopolymer particles (TEP), as well as dissolved organic carbon (DOC) and nitrogen (DON), in addition to carbonate system parameters at CO2 levels of 180, 380 and 750 µatm. No significant difference between treatments was observed for any of the measured variables during repeated sampling over a 14 d period. We considered several factors that might lead to these results, i.e. light, nutrients, carbon overconsumption and transient versus steady-state growth. We suggest that the absence of a clear CO2 effect during this study does not necessarily imply the absence of an effect in nature. Instead, the sensitivity of the cell towards environmental stressors such as CO2 may vary depending on whether growth conditions are transient or sufficiently stable to allow for optimal allocation of energy and resources. We tested this idea on previously published data sets where PIC and POC divided by the corresponding cell abundance of E. huxleyi at various pCO2 levels and growth rates were available.
    Keywords: Abundance per volume; Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Bicarbonate ion; BIOACID; Biological Impacts of Ocean Acidification; Biomass/Abundance/Elemental composition; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calcite saturation state, standard deviation; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, particulate, per cell; Carbon, organic, dissolved, per cell; Carbon, organic, dissolved/Nitrogen, organic, dissolved ratio; Carbon, organic, particulate, per cell; Carbon, organic, particulate, standard deviation; Carbon, organic, particulate/Nitrogen, particulate ratio; Carbon, organic, particulate/Nitrogen, particulate ratio, standard deviation; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, partial pressure; Chlorophyll a, standard deviation; Chlorophyll a per cell; Chromista; Day of experiment; Emiliania huxleyi; Emiliania huxleyi, standard deviation; Figure; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Haptophyta; Laboratory experiment; Laboratory strains; Nitrogen, organic, dissolved, per cell; Nitrogen, particulate, per cell; Nitrogen, total, particulate/Phosphorus, organic, particulate, ratio; Nitrogen, total, particulate/Phosphorus, organic, particulate, ratio, standard deviation; Not applicable; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Particulate inorganic carbon/particulate organic carbon ratio; Particulate inorganic carbon/particulate organic carbon ratio, standard deviation; Pelagos; pH; pH, standard deviation; Phosphorus, organic, particulate, per cell; Phytoplankton; Salinity; Single species; Species; Standard deviation; Temperature, water
    Type: Dataset
    Format: text/tab-separated-values, 3723 data points
    Location Call Number Limitation Availability
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