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Seawater carbonate chemistry and changes in isotope fractionation during nitr...
We measured N and O isotope effects during nitrate assimilation and physiological states of the marine diatom Thalassiosira weissflogii and Synechococcus under different pH (8.1... -
Elemental and biochemical contents of the diets of the copepod Temora longico...
This dataset has no description
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Seawater carbonate chemistry, POC, PIC, TPC, SPM, N, TEP and growth rate duri...
The response of three coccolithophores (Emiliania huxleyi, Calcidiscus leptoporus and Syracosphaera pulchra) to elevated partial pressure (pCO2) of carbon dioxide was... -
Seawater carbonate chemistry and biological processes during experiments with...
The response of Emiliania huxleyi (Lohmann), Calcidiscus leptoporus (Murray and Blackman), and Syracosphaera pulchra (Lohmann) to elevated partial pressure of carbon dioxide... -
Seawater carbonate chemistry and processes during experiments with cyanobacte...
The surface ocean absorbs large quantities of the CO2 emitted to the atmosphere from human activities. As this CO2 dissolves in seawater, it reacts to form carbonic acid. While... -
Seawater carbonate chemistry and growth rates, physiology, and geneexpression...
Heterosigma akashiwo is a raphidophyte known for forming ichthyotoxic blooms. In order to predict the potential impacts of rising CO2 on H. akashiwo it is necessary to... -
Grazing rates of Temora longicornis under different nutrient regimes
This dataset has no description
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Elemental cellular contents of Rhodomonas salina and Oxyrrhis marina, and res...
This dataset contains data on the cellular elemental contents (carbon, nitrogen and phosphorus) of the phytoplankton species Rhodomonas salina grown in nitrogen limited and... -
Ocean acidification affects the phyto-zoo plankton trophic transfer efficiency
The critical role played by copepods in ocean ecology and biogeochemistry warrants an understanding of how these animals may respond to ocean acidification (OA). Whilst an... -
Cellular elemental stoichiometry of two phytoplankton species, Rhodomonas sal...
Cellular elemental stoichiometry of two phytoplankton species, Rhodomonas salina and Teleaulax sp., grown in nutrient replete F/2 medium and in P-limited conditions, as well as... -
(Supplement 2) Phytoplankton and dinoflagellate stoichiometry in the Microsco...
This dataset comprises data from two experiments analysed with two different tools, a FlowCam and a microscope. The heterotrophic dinoflagellate Oxyrrhis marina was subjected to... -
(Supplement 1) Phytoplankton and dinoflagellate stoichiometry in the FlowCam ...
This dataset comprises data from two experiments analysed with two different tools, a FlowCam and a microscope. The heterotrophic dinoflagellate Oxyrrhis marina was subjected to... -
Carbon and nitrogen contents of the diet of Temora longicornis under differen...
This dataset has no description
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Lack of evidence for elevated CO2-induced bottom-up effects on marine copepod...
Rising levels of atmospheric CO2 are responsible for a change in the carbonate chemistry of seawater with associated pH drops (acidification) projected to reach 0.4 units from... -
Seawater carbonate chemistry and processes during experiments with Emiliania ...
We have measured the stable carbon isotopic composition of bulk organic matter (POC), alkenones, sterols, fatty acids, and phytol in the coccolithophorid Emiliania huxleyi grown... -
Seawater carbonate chemistry and particulate organic particles during a semic...
Diazotrophic (N2-fixing) cyanobacteria provide the biological source of new nitrogen for large parts of the ocean. However, little is known about their sensitivity to global...
