-
Sporolithon sp2 structural integrity responses across the PETM
This dataset contains cell measurements (length, width and wall thickness) for an unidentified coralline alga of the genus Sporolithon, labelled Sporolithon sp2. Samples were... -
Sporolithon sp1 structural integrity responses across the PETM
This dataset contains cell measurements (length, width and wall thickness) for an unidentified coralline alga of the genus Sporolithon, labelled Sporolithon sp1. Samples were... -
Sporolithon aschersonii structural integrity responses across the PETM
This dataset contains cell measurements (length, width and wall thickness) for the coralline alga Sporolithon aschersonii. Samples were extracted from limestone collected in... -
Lithothamnion roveretoi structural integrity responses across the PETM
This dataset contains cell measurements (length, width and wall thickness) for the coralline alga Lithothamnion roveretoi. Samples were extracted from limestone collected in... -
Long-term dynamics of adaptive evolution in a globally important coccolithoph...
In order to allow full comparability with other ocean acidification data sets, the R package seacarb (Lavigne et al, 2014) was used to compute a complete and consistent set of... -
Seawater carbonate chemistry and calcification of an estuarine coccolithophore
Ocean acidification has the capacity to impact future coccolithophore growth, photosynthesis, and calcification, but experimental culture work with coccolithophores has produced... -
The effect of phosphorus limitation and heat stress on calcification in Emili...
Calcifying haptophytes (coccolithophores) sequester carbon in the form of organic and inorganic cellular components (coccoliths). We examined the effect of phosphorus (P)... -
Differing responses of three Southern Ocean Emiliania huxleyi ecotypes to cha...
The invasion of anthropogenic carbon dioxide into the surface ocean is altering seawater carbonate speciation, a process commonly called ocean acidification. The high latitude... -
Seawater carbonate chemistry and specific growth rate, respiration rate, net ...
Experimentally elevated pCO2 and the associated pH drop are known to differentially affect many aspects of the physiology of diatoms under different environmental conditions or... -
Seawater carbonate chemistry and nitrogen fixation by phosphorus-limited Tric...
Growth of the prominent nitrogen-fixing cyanobacterium Trichodesmium is often limited by phosphorus availability in the ocean. How nitrogen fixation by phosphorus-limited... -
Seawater carbonate chemistry and morphology and nutrient physiology of the co...
We investigated the effect of decreased pH on the morphology and nutrient physiology of the cosmopolitan marine diatom Thalassiosira rotula (CCMP3362) by acclimating unialgal... -
Seawater carbonate chemistry and water content, apoptosis, and proliferation ...
Here, we studied structural changes in medaka (Oryzias melastigma) brain regions contacting cerebrospinal fluid (CSF) after short-term (7 days) CO2 exposure. This dataset is... -
Growth responses of Skeletonema marinoi-dohrnii complex and Chattonella marin...
Growth responses of Skeletonema marinoi-dohrnii complex and Chattonella marina isolated from Japanese coastal waters were monitored under different nitric oxide (NO) supply... -
Growth rates and biometric measurements of coccolithophores (Coccolithus pela...
Coccolithophores, a diverse group of phytoplankton, make important contributions to pelagic calcite production and export, yet the comparative biogeochemical role of species... -
Growth rates of various ciliates determined experimentally
This dataset has no description
-
Feeding rates of Ciliates on Heterocapsa triquetra determined experimentally
This dataset has no description
-
Feeding and growth rates of Favella sp. determined experimentally
Carbon per cell of prey 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 the marine planktonic ciliate Strombidin...
Carbon per cell of grazer calculated using the following equation of Menden-Deuer and Lessard (2000): picogram carbon per cell = 0.216biovolume*0.939. -
Growth rate of the marine planktonic ciliate Strombidinopsis cheshiri determi...
Carbon per cell of grazer calculated using the following equation of Menden-Deuer and Lessard (2000): picogram carbon per cell = 0.216biovolume*0.939. -
Growth response of the genera Strobilidium and Strombidium determined experim...
Carbon per cell of grazer calculated using the following equation of Menden-Deuer and Lessard (2000): picogram carbon per cell = 0.216biovolume*0.939.
