CYLINDROSPERMOPSIS RACIBORSKII (CYANOBACTERIA) INVASION AT MID‐LATITUDES: SELECTION, WIDE PHYSIOLOGICAL TOLERANCE, ORGLOBALWARMING? 1

By J. Briand, C. Leboulanger, J. Humbert, C. Bernard, P. Dufour. 2004

354 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics, Environmental Chemistry, Renewable Energy, Sustainability and the Environment

View Paper: https://www.semanticscholar.org/paper/0d2a6f11747a91c68093d41884a0b00606ea55d4

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Citations in the corpus

Climate change: links to global expansion of harmful cyanobacteria. (2012, background): “…connection between eutrophication and CyanoHABs expansion is well-established (Fogg, 1969; Paerl, 1988; Reynolds, 2006; Paerl and Fulton, 2006), climatic changes have also been implicated (Briand et al., 2004; Elliott et al., 2005, 2006; Paerl and Huisman, 2008; Paul, 2008; Paerl et al., 2011a,b).”
Distribution of three alien cyanobacterial species (Nostocales) in northeast Germany: Cylindrospermopsis raciborskii, Anabaena bergii and Aphanizomenon aphanizomenoides (2006, background): “There is controversial evidence whether its obvious ecological success is due to selection mechanisms (Chonudomkul et al. 2004), based on a wide physiological tolerance coupled with global warming (Briand et al. 2004), or due to radiation processes after the last glaciations (Gugger et al. 2005).”
Algal bloom and its economic impact (2016, background): “This is the example of Cylindrospermopsis raciborskii which was originally found in Australia and Central Africa while at present it has been observed in Europe and in United States of America (USA), suggesting a link between eutrophication and warmer temperature [63, 64].”
Harmful Algal Blooms (2015, background): “…by a combination of eutrophication and climate change, as seen with the toxin-producing Cylindrospermopsis raciborskii, historically considered a tropical taxa, which has colonized eutrophic lakes in North America and worldwide (Briand et al., 2004; Mehnert et al., 2010; Bonilla et al., 2012).”
DOES ALLELOPATHY CONTRIBUTE TO CYLINDROSPERMOPSIS RACIBORSKII (CYANOBACTERIA) BLOOM OCCURRENCE AND GEOGRAPHIC EXPANSION? 1 (2007, background): “…capitalize on the cheapest N-source while other heterocytic species must fix N2; (5) resistance to grazing due to toxicity; (6) buoyancy control; (7) ability to form akinetes, allowing easy dispersal and environmental resistance (Padisák 1997); and (8) wide thermal tolerance (Briand et al. 2004).”
Climate change: a catalyst for global expansion of harmful cyanobacterial blooms. (2009, background): “It was first described in France in 1994 (Briand et al., 2004), in Portugal in the late 1990s (Saker et al.”
Effects of light intensity on cylindrospermopsin production in the cyanobacterial HAB species Cylindrospermopsis raciborskii (2006, methodology): “Maximum CYN production was also found to occur at 20°C (Saker and Griffiths 2000), whereas maximum growth rates occurred between 29°C and 35°C (Briand et al. 2004).”
Cylindrospermopsin is not degraded by co-occurring natural bacterial communities during a 40-day study (2008, background): “Among these species, the most widely distributed is Cylindrospermopsis raciborskii, which is now found in many countries (Briand et al., 2004).”
Growth at the edge of the niche: An experimental study of the harmful alga Prymnesium parvum (2009, background): “Here, we focus on growth of P. parvum at the edge of the niche, in terms of salinity, an uncommon approach but one that may be valuable for understanding invasive species (Briand et al. 2004).”
The ecology of the invasive cyanobacterium Cylindrospermopsis raciborskii (Nostocales, Cyanophyta) in two hypereutrophic lakes dominated by Planktothrix agardhii (Oscillatoriales, Cyanophyta) (2010, background): “Temperature has been considered the major limiting factor for growth of C. raciborskii (Pádisak, 1997; Wiedner et al., 2007), with its optimal growth rate in laboratory experiments being at 25–35 C (Saker & Griffiths, 2000; Briand et al., 2004; Castro et al., 2004; Chonudomkul et al., 2004).”
Phytoplankton community in the tropical lake of Lagoa Santa (Brazil): Conditions favoring a persistent bloom of Cylindrospermopsis raciborskii (2009, background): “2002); N2-fixation; high affinity for ammonium, allowing it to capitalize on the cheapest N source while other heterocytic species must fix N2; resistance to grazing due to toxicity; buoyancy control; ability to form akinetes, allowing easy dispersal and environmental resistance (Padis ak 1997), wid”
Phytoplankton species succession in a shallow Mediterranean lake (L. Kastoria, Greece): steady-state dominance of Limnothrix redekei, Microcystis aeruginosa and Cylindrospermopsis raciborskii (2006, background): “It is well known that C. raciborskii has a high temperature optimum for growth (20–30 C) (e.g. Briand et al., 2004) and can tolerate low light availability in warm mixed layers (Reynolds et al., 2002).”
Toxicity of Aphanizomenon ovalisporum (Cyanobacteria) in a Spanish water reservoir (2006, background): “Among these species the most widely distributed is Cylindrospermopsis raciborskii, which is now found in many countries (Briand et al., 2004).”
A review of the alien and expansive species of freshwater cyanobacteria and algae in the Czech Republic (2010, background): “…in India and Thailand (Komárek and Komárková 2003), Japan (Chonudomkul et al. 2004), the Philippines, Egypt (Komárek and Komárková 2003), Senegal (Briand et al. 2004), Brazil (Bouvy et al. 2000; Molica et al. 2002), Cuba (Komárek and Komárková 2003), Chile (Lagos 1998), Uruguay (Vidal…”