Approaches for determining phytoplankton nutrient limitation
By John Beardall, E. Young, S. Roberts. Aquatic Sciences, 2001
324 citations recorded by the source corpus.
Subfields: Ecology, Environmental Chemistry, Oceanography
View Paper: https://www.semanticscholar.org/paper/55d960b8ef90194e9e797371b7e6a83cd69c00e4
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In Ecology
- Sonya T. Dyhrman
- T. Andersen
- Timo Tamminen
- K. Ruttenberg
- S. Duhamel
- R. Geider
- M. Borowitzka
- David M. Karl
In Environmental Chemistry
- Sonya T. Dyhrman
- K. Ruttenberg
- T. Andersen
- Timo Tamminen
- M. Borowitzka
- R. Geider
- N. Leonardos
- Navid R. Moheimani
In Oceanography
- Sonya T. Dyhrman
- M. Borowitzka
- K. Ruttenberg
- Timo Tamminen
- T. Andersen
- R. Geider
- Navid R. Moheimani
- S. Duhamel
Citations in the corpus
- Presence and regulation of alkaline phosphatase activity in eukaryotic phytoplankton from the coastal ocean: Implications for dissolved organic phosphorus remineralization (2006, methodology): “…interpretation of community APA as a P deficiency indicator and necessitates the use of multiple indicators and/or nutrient-addition experiments in order to confidently assign the nutrient-deficiency status of a population (Healey and Hendzel 1979; Rose and Axler 1998; Beardall et al. 2001).”
- Alkaline phosphatase activity and regulation in the North Pacific Subtropical Gyre (2010, background): “The extent to which these Pstressed cells are able to scavenge P will result in either P limitation or recovery (Beardall et al. 2001; Dyhrman and Ruttemberg 2006).”
- Nutrient limitation of picophytoplankton photosynthesis and growth in the tropical North Atlantic (2008, background): “Use of bioassay experiments to assess nutrient limitation has sometimes been questioned on the basis of perceived flaws in the experimental design and/or perceived limitations imposed by confining natural phytoplankton communities in bottles (Beardall et al. 2001).”
- A comparison of methods for detection of phosphate limitation in microalgae (2001, methodology): “FT-IR MS analysis indicates that Sphaerocystis, Phormidium and Nitzschia all showed alterations in the storage of carbon, in response to changes in nutrient availability, similar to those reported elsewhere using conventional methods (see Beardall et al., 2001).”
- Sustainable biofuels from algae (2013, background): “The average elemental composition of freshwater algae is CH1.7O0.4N0.15P0.0094 (Oswald 1988), although the N content in particular will vary somewhat with the environmental conditions and nutrient status of the algae (e.g., Beardall et al. 2001; Berges et al. 2002).”
- Seasonal phytoplankton nutrient limitation patterns as revealed by bioassays over Baltic Sea gradients of salinity and eutrophication (2007, methodology): “Methods for verifying the limitation pattern of this domain all carry inherent constraints, which also relate to the temporal and spatial scales of the processes involved (e.g. Beardall et al. 2001).”
- Responses of elemental and biochemical composition of Chaetoceros muelleri to growth under varying light and nitrate : phosphate supply ratios and their influence on critical N: P (2004, background): “There are two distinctively different types of limitation: one referring to limitation of the maximum population density achieved (Liebig limitation) and one referring to limitation of growth rates (Blackman limitation, Perry 1976; Beardall et al. 2001).”