Competition for nutrients and light: Stable coexistence, alternative stable states or competitive exclusion?

By J. Passarge, S. Hol, M. Escher, J. Huisman. 2006

228 citations recorded by the source corpus.

Subfields: Environmental Chemistry, Genetics, Global and Planetary Change

View Paper: https://www.semanticscholar.org/paper/794bfe5de1830ed79299bc8e3b6291ade5c221f2

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Citations in the corpus

Competition and facilitation between unicellular nitrogen‐fixing cyanobacteria and non—nitrogen‐fixing phytoplankton species (2007, methodology): “More precisely, we fitted time courses predicted by the model to the time courses of population density (Pi), light transmission (Iout), and nitrogen concentration (R) measured in the monoculture experiments (Huisman et al. 1999; Passarge et al. 2006).”
Summer heatwaves promote blooms of harmful cyanobacteria (2008, methodology): “The model structure is firmly based on well-tested physical models (Svensson, 1978; Jöhnk & Umlauf, 2001; Peeters et al., 2007a) and plankton models (Huisman et al., 1999a, b, 2004; Passarge et al., 2006).”
Trait-Based Community Ecology of Phytoplankton (2008, background): “Phytoplankton need to overcome significant diffusion limitation on resources (Pasciak & Gavis 1974, Raven 1980) and to maintain themselves in the water column to have access to light, despite sinking.”
Influence of water‐column depth and mixing on phytoplankton biomass, community composition, and nutrients (2008, background): “…the light intensity at the bottom of the water column to the lowest level and the limiting nutrients to the lowest concentrations will then displace all other competitors, allowing at best a few species to persist in the long run (Sommer 1985; Huisman and Weissing 1995; Passarge et al. 2006).”
Linking modern coexistence theory and contemporary niche theory (2017, background): “The key papers, including Tilman (1982), Chase and Leibold (2003) and Chesson (2000b),”
A biodiversity‐inspired approach to aquatic ecosystem modeling (2007, background): “If the mechanisms underlying our trade-off are real, its subtlety could explain why the existence of a trade-off between light and nutrient harvesting has as yet not been convincingly demonstrated (Huisman and Weissing 2001; Passarge et al. 2006).”
Light and growth in marine phytoplankton: allometric, taxonomic, and environmental variation (2015, background): “Some support for these predictions comes from lab experiments on competition for light (Huisman and Weissing 1999, Passarge et al. 2006), the existence of high vs. low light ecotypes (Moore and Chisholm 1999, Rodriguez et al. 2005), depth-stratified community structure (Furuya and Marumo 1983,…”
Stoichiometrically Explicit Food Webs: Feedbacks between Resource Supply, Elemental Constraints, and Species Diversity (2009, background): “For instance, they can resist or tolerate herbivory, and they compete with each other for nutrients and light (e.g., DeMott & Tessier 2002, Grover 1997, Passarge et al. 2006).”
Elevated CO2 concentrations affect the elemental stoichiometry and species composition of an experimental phytoplankton community (2013, result): “1 lM in our high CO2 treatment is of similar order of magnitude as R* values for phosphorus reported in previous studies (e.g. Tilman, 1977; Van Donk & Kilham, 1990; Passarge et al., 2006), while the phosphorus concentrations in our moderately elevated CO2 treatment and the control experiment were h”