Phytoplankton nutrient competition under dynamic light regimes

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Trait-Based Community Ecology of Phytoplankton (2008, background): “A high maximum growth rate can be advantageous under fluctuating resource supplies and can lead to either the competitive displacement of slowgrowing good competitors or stable coexistence (Grover 1991a,b; Litchman & Klausmeier 2001).”
Dreissenid Phosphorus Excretion Can Sustain C. glomerata Growth Along a Portion of Lake Ontario shoreline (2009, methodology): “Clear chambers were used to ensure phosphorus uptake by phytoplankton and periphyton was maintained during incubations (Reigman et al., 2000; Litchman et al., 2004), as well as to minimize disturbance of dreissenids (Morton, 1969), making our results close to net daytime nutrient uptake and excretio”
Ecological Networks in a Changing Climate (2010, unknown): “For instance, phytoplankton growth physiology has been extensively studied using chemostats and modelled using a range of generalizations (e.g. Klausmeier et al., 2004a,b; Litchman et al., 2004; White and Zhao, 2009) of the classic Droop model (Droop, 1983) of nutrient uptake and growth.”
Phytoplankton motility and the competition for nutrients in the thermocline (2007, background): “Diatoms exhibit relatively high uptake rates when exposed to light and lower rates in darkness, especially for nutrients such as nitrate that require more energy to be assimilated (Eppley et al. 1971, Dortch & Maske 1982, Litchman et al. 2004).”