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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... -
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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Seawater carbonate chemistry and phytoplankton, copepod development, and fatt...
Change in the nutritional quality of phytoplankton is a key mechanism through which ocean acidification can affect the function of marine ecosystems. Copepods play an important... -
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... -
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... -
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... -
Nano- and microplankton in the northern Patagonian shelf (SW South Atlantic) ...
The species composition and structure (e.g. abundance and biomass) of protistan plankton (cell size > 5 µm) and in situ chorophyll a were assessed in a shallow (<50 m... -
Prokaryotic respiration and growth in Baltic and north Seas 2017
Data was collected in a project investigating the importance of prokaryotic maintenance respiration in the marine environment. Prokaryotic respiration, growth and abundance was... -
Plankton data from 2017 mesocosm experiment manipulating nutrient concentrati...
Data from a mesocosm experiment where the effects of nitrate and phosphate fertilization and copepod grazing pressure on Baltic sea plankton community were followed. Oversupply... -
Plankton data from 2016 mesocosm experiment manipulating Si:N and copepod gra...
Phytoplankton, microzooplankton, copepod and dissolved nutrient data from a mesocosm experiment, which took place in summer 2016. A range of Si:N ratios and two levels of... -
Feeding rates of Favella sp. and Balanion sp. determined experimentally
Carbon per cell of grazer Balanion sp. calculated using the following equation of Menden-Deuer and Lessard (2000): picogram carbon per cell = 0.216biovolume*0.939. -
Feeding, growth and grazing rates of Strombidium sulcatum determined experime...
Carbon per cell of prey and grazer calculated using the following equation of Menden-Deuer and Lessard (2000): picogram carbon per cell = 0.216biovolume*0.939.
