Allelopathic effect of Prymnesium parvum on a natural plankton community
By Giovana O. Fistarol, C. Legrand, E. Granéli. 2003
259 citations recorded by the source corpus.
Subfields: Environmental Chemistry, Oceanography
View Paper: https://www.semanticscholar.org/paper/a9f96968ba802a23a318a18eabed2c48612cbd91
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In Environmental Chemistry
- E. Granéli
- C. Gobler
- Paulo S. Salomon
- P. J. Hansen
- U. Tillmann
- Giovana O. Fistarol
- Y. Tang
- Martin Weberg
In Oceanography
- E. Granéli
- C. Gobler
- Y. Tang
- P. J. Hansen
- Giovana O. Fistarol
- U. Tillmann
- Paulo S. Salomon
- S. Suikkanen
Citations in the corpus
- Phytoplankton blooms: a ‘loophole’ in microzooplankton grazing impact? (2005, background): “A number of species may be able to enter such a loophole at that point in time and space but the best equipped phytoplankton species starts to bloom, consuming nutrients and perhaps releasing allelopathic chemicals inhibiting the growth of competitors (Fistarol et al., 2003, 2004).”
- A chronicle of a killer alga in the west: ecology, assessment, and management of Prymnesium parvum blooms (2015, background): “While it is capable of supporting population growth through autotrophy, it can also support growth through heterotrophy, employing both saprophytic and phagocyticmodes of nutrition (Fistarol et al., 2003; Skovgaard &Hansen, 2003; Tillmann, 2003; Granéli & Johansson, 2003a).”
- Allelopathic effects of the Baltic cyanobacteria Nodularia spumigena, Aphanizomenon flos-aquae and Anabaena lemmermannii on algal monocultures (2004, background): “parvum (Fistarol et al., 2003).”
- Phytoplankton community ecology: principles applied in San Francisco Bay (2005, unknown): “Some algae synthesize multiple compounds which inhibit growth of bacteria, other phytoplankton, protozoan and metazoan grazers (Fistarol et al. 2003) to structure planktonic communities from both the top down and bottom up.”
- POSITIVE FEEDBACK AND THE DEVELOPMENT AND PERSISTENCE OF ECOSYSTEM DISRUPTIVE ALGAL BLOOMS 1 (2006, background): “…h/d except where noted. bW. G. Sunda and D.R. Hardison (unpublished data). cCells and cell extracts elicit toxic activity, but no toxin has been identified (Gainey and Shumway 1991, Buskey and Hyatt 1995, Liu and Buskey 2000, Bricelj et al. 2001, Greenfield and Lonsdale 2002). d16 h/d photoperiod.”
- Allelopathy in Alexandrium spp.: effect on a natural plankton community and on algal monocultures (2004, background): “…where the allelo- 52 Fistarol et al.: Allelopathy in Alexandrium spp. pathic algae cause very strong negative effects, such as Prymnesium parvum, most phytoplankton organisms die causing a decline in the plankton community, which is unable to maintain a positive growth rate (Fistarol et al. 2003).”
- Allelopathic effects of Cochlodinium polykrikoides isolates and blooms from the estuaries of Long Island, New York, on co-occurring phytoplankton. (2010, background): “…are also known to have allelopathic impacts on other algae, including Karenia brevis (Kubanek et al. 2005, Prince et al. 2008), Prymnesium parvum (Fistarol et al. 2003, Granéli & Johansson 2003, Tillmann 2003), Alexandrium spp. (Arzul et al. 1999, Tillmann & John 2002, Fistarol et al. 2004),…”
- Harmful algal blooms of allelopathic microalgal species: The role of eutrophication (2008, background): “Thus, the decline in cell densities of the phytoplankton species exposed to these filtrates can be accounted for by the toxicity of the excreted allelochemicals (Fistarol et al., 2003; Granéli and Johansson, 2003; Tillmann, 2003; Skovgaard and Hansen, 2003).”
- Phagotrophy in harmful algae (2006, background): “Like C. polylepis, Prymnesium parvum is known to severely affect other plankton organisms, as has been shown using algal cultures (Graneli and Johansson 2003b), heterotrophic protists (Graneli and Johansson 2003a; Rosetta and McManus 2003; Tillmann 2003) and natural communities ( Fistarol et al. 200”
- Allelopathic effect on a nutrient-limited phytoplankton species (2005, background): “Consequences for the outcome of allelopathic interactions It has been shown that some microalgae can cause allelopathy under non-limiting nutrient conditions (Arzul et al. 1999, Schmidt & Hansen 2001, Tillmann & John 2002, Fistarol et al. 2003, 2004, Suikkanen et al. 2004).”
- Effects of nutrient enrichment on Prymnesium parvum population dynamics and toxicity: results from field experiments, Lake Possum Kingdom, USA (2007, background): “These included inhibition of competitors through production of allelopathic chemicals (Fistarol et al. 2003, 2005, Granéli & Johansson 2003a, Barreiro et al. 2005, Uronen et al. 2005), mortality or grazing inhibition to predators through production of toxic chemicals (Granéli & Johansson 2003b,…”
- Effects of cyanobacterial allelochemicals on a natural plankton community (2005, background): “Cyanobacteria may not cause as dramatic growth inhibition of Baltic Sea microplankton as, for example, the haptophyte Prymnesium parvum (Fistarol et al. 2003), but they seem able to reduce the growth of some taxa while increasing others, and thus cause significant changes in the plankton…”
- Does the red tide dinoflagellate Karenia brevis use allelopathy to outcompete other phytoplankton? (2005, background): “Understanding the community-wide effects of competition and allelopathy requires field experimentation, or at least the use of field assemblages of phytoplankton (e.g., Fistarol et al. 2003).”
- Harmful Algal Blooms (2015, background): “Although ecological impacts of P. parvum are most commonly reported as fish kills, some prymnesins also appear to act as allelogens against co-occurring phytoplankton (Fistarol et al., 2003; Granéli and Johansson, 2003; Brooks et al., 2010).”