Allelopathy in the prymnesiophyte Chrysochromulina polylepis: effect of cell concentration, growth phase and pH

By Lisanna Schmidt, P. J. Hansen. 2001

198 citations recorded by the source corpus.

Subfields: Environmental Chemistry, Molecular Biology, Oceanography

View Paper: https://www.semanticscholar.org/paper/87a7c95f4020213109945bc60a84cbb39a73ddb8

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Citations in the corpus

Allelopathy in Alexandrium spp.: effect on a natural plankton community and on algal monocultures (2004, methodology): “Schmidt & Hansen (2001) also suggested that the release of chemical compounds by C. polylepis could indeed explain a bloom like the one in 1988, although other factors such as pH and perhaps CO2 affect the toxicity of C. polylepis, and must be taken into consideration.”
Allelopathic interactions between the bacillariophyte Skeletonema costatum and the raphidophyte Heterosigma akashiwo (2007, background): “Effects of pH on growth of 4 phytoplankton species Recently, some studies indicated that elevated pH in culture media inhibited the growth of phytoplankters in mixed cultures (Goldman et al. 1981, 1982, Schmidt & Hansen 2001, Lundholm et al. 2005).”
Does the red tide dinoflagellate Karenia brevis use allelopathy to outcompete other phytoplankton? (2005, methodology): “First, using mixed culture competition experiments (e.g., Schmidt and Hansen 2001) or field observations of species composition (e.g., Vardi et al. 2002), it is impossible to distinguish allelopathy from other mechanisms, such as exploitation competition.”
Effect of pH on growth and domoic acid production by potentially toxic diatoms of the genera Pseudo-nitzschia and Nitzschia (2004, background): “These results support previous findings of pH as a limiting factor for growth of other microalgae grown in 7 Mar Ecol Prog Ser 273: 1–15, 2004 nutrient-rich media such as f/2 growth medium (e.g. Schmidt & Hansen 2001, Hansen 2002, Hinga 2002).”
Allelopathic effects of Alexandrium tamarense on other algae: evidence from mixed growth experiments. (2009, background): “Such experiments are not trivial, because a number of factors may influence their outcome (see Schmidt & Hansen 2001), making interpretations difficult.”
Harmful algal blooms of allelopathic microalgal species: The role of eutrophication (2008, background): “studies on haptophytes (Myklestad et al., 1995; Schmidt and Hansen, 2001) and dinoflagellates (Tillmann et al.”
GROWTH INHIBITION AND TOXICITY OF THE DIATOM ALDEHYDE 2‐TRANS, 4‐TRANS‐DECADIENAL ON THALASSIOSIRA WEISSFLOGII (BACILLARIOPHYCEAE) 1 (2005, background): “In phytoplankton, toxin production is usually related to the growth phase (i.e. actively growing or senescent cells) (Schmidt and Hansen 2001) or life or cell cycle stage (Taroncher-Oldenburg et al. 1997).”
Increase in the production of allelopathic substances by Prymnesium parvum cells grown under N- or P-deficient conditions (2003, background): “Schmidt and Hansen (2001) also found that C. polylepis had a strong allelopathic effect on the dinoflagellate Heterocapsa triquetra ,b ut that this effect was also coupled to pH. The ability of P. parvum to excrete toxic substances was demonstrated almost three decades ago (Shilo, 1971).”
Allelopathic effect on a nutrient-limited phytoplankton species (2005, background): “It has been shown that the allelopathic effect of Chrysochromulina polylepis on Heterocapsa triquetra increases if the pH is raised, with the highest effect being observed at a pH between 8 and 9, depending on the cell concentration of C. polylepis (Schmidt & Hansen 2001).”