POSITIVE FEEDBACK AND THE DEVELOPMENT AND PERSISTENCE OF ECOSYSTEM DISRUPTIVE ALGAL BLOOMS 1

By W. Sunda, E. Granéli, C. Gobler. 2006

266 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/b8ae9855aa713b7b0b746f2a4c2aa98bfed47072

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In Oceanography

Citations in the corpus

Eutrophication and Harmful Algal Blooms: A Scientific Consensus (2008, background): “Increased nutrient enrichment can lead to a shift in plankton community composition, which in turn can afect predator–prey relationships, further altering the transfer of nutrients (e.g., Smayda, 1989; MacIntyre et al., 2004; Irigoien et al., 2005; Mitra and Flynn, 2006; Sunda et al., 2006).”
Characterization of the toxicity of Cochlodinium polykrikoides isolates from Northeast US estuaries to finfish and shellfish. (2009, background): “, 2001), which tend to bemaximal and accumulate when cell growth declines (Sunda et al., 2006).”
Effects of changing pCO2 and phosphate availability on domoic acid production and physiology of the marine harmful bloom diatom Pseudo‐nitzschia multiseries (2011, background): “In general, many harmful algal species often show increased toxin production when their growth is limited by nutrients (Sunda et al. 2006).”
Growth at the edge of the niche: An experimental study of the harmful alga Prymnesium parvum (2009, background): “There is a perception that the frequency of such blooms has increased over recent decades (Hallegraeff 1993; Sunda et al. 2006), perhaps due to ongoing eutrophication, aquaculture, and other anthropogenic changes.”
The role of nitrogenous nutrients in the occurrence of harmful algal blooms caused by Cochlodinium polykrikoides in New York estuaries (USA) (2012, background): “While many HABs do not directly harm aquatic organisms, others can be lethal (Landsberg, 2002; Sunda et al., 2006).”
Ecological Stoichiometry, Biogeochemical Cycling, Invasive Species, and Aquatic Food Webs: San Francisco Estuary and Comparative Systems (2011, background): “The dominance of such species can result in a failure of normal predator–prey interactions, which, in turn, enhances the transfer of nutrients that sustain the harmful algal blooms at the expense of competing algal species (Irigoien et al., 2005; Mitra and Flynn, 2006; Sunda et al., 2006).”
Allelopathic effects of Cochlodinium polykrikoides isolates and blooms from the estuaries of Long Island, New York, on co-occurring phytoplankton. (2010, background): “Allelopathic effects on competitors, together with grazing deterrence, could promote C. polykrikoides blooms through positive feedback (Sunda et al. 2006), whereby higher C. polykrikoides cell densities yield fewer competitors and predators, which, in turn, facilitates higher cell densities.”
Linking traits to species diversity and community structure in phytoplankton (2010, background): “Therefore , it would be useful to develop trait-based approaches to explain and predict the occurrence of HABs in diverse ecosystems.”
OCEAN CLIMATE CHANGE, PHYTOPLANKTON COMMUNITY RESPONSES, AND HARMFUL ALGAL BLOOMS: A FORMIDABLE PREDICTIVE CHALLENGE 1 (2010, background): “…algal blooms of, for example, Aureococcus, Chrysochromulina, Prymnesium, and Nodularia have recently been referred to as ecosystem disruptive algal blooms (EDABs), in which toxic or unpalatable algal species disrupt grazing and thus diminish nutrient supply via recycling (Sunda et al. 2006).”
Complexity in the eutrophication–harmful algal bloom relationship, with comment on the importance of grazing (2008, background): “The mixotrophy of Aureococcus is expected to influence the extent to which its putative husbandry of blooms through grazer feedback control mechanisms (Sunda et al., 2006) is realized.”
The role of mixotrophic protists in the biological carbon pump (2013, unknown): “In essence, the dominance of the mixotrophs in the P-limited high N : P system developed through a process not dissimilar to that proposed by Mitra and Flynn (2006b) for the formation of an ecosystem-disruptive harmful algal bloom (EDAB; Sunda et al., 2006).”
Harmful dinoflagellate blooms caused by Cochlodinium sp.: Global expansion and ecological strategies facilitating bloom formation (2012, background): “Although many HABs are thought to be caused by factors that enhance cellular growth rates such as nutrients, light, and temperature, an absence of strong top down control by grazing populations may also contribute towards bloom formation (Gobler et al., 2002; Sunda et al., 2006; Smayda, 2008).”