59. El-Sheekh MM, Dawah AM, Abd El-Rahman AM, El-Adel HM, Abd El-Hay RA (2008)
Antimicrobial activity of the cyanobacteria Anabaena wisconsinense and Oscillatoria
curviceps against pathogens of fish in aquaculture. Ann Microbiol 58:527–534
60. Jonas A, Buranova V, Scholz S, Fetter E, Novakova K, Kohoutek J, Hilscherova K (2014)
Retinoid-like activity and teratogenic effects of cyanobacterial exudates. Aquat Toxicol
155:283–290
61. Jonas A, Scholz S, Fetter E, Sychrova E, Novakova K, Ortmann J, Benisek M, Adamovsky O,
Giesy JP, Hilscherova K (2015) Endocrine, teratogenic and neurotoxic effects of cyanobacteria
detected by cellular in vitro and zebrafish embryos assays. Chemosphere 120:321–327
62. Zagatto PA, Buratini S, Aragão MA, Ferrão-Filho AS (2012) Neurotoxicity of two Cylindrospermopsis raciborskii (cyanobacteria) strains to mice, Daphnia, and fish. Environ Toxicol
Chem 31:857–862
63. Otten TG, Paerl HW (2015) Health effects of toxic cyanobacteria in U.S. drinking and
recreational waters: our current understanding and proposed direction. Curr Environ Health
Rep 2:75–84
64. Carmichael WW (1992) Cyanobacteria secondary metabolites – the cyanotoxins. J Appl
Bacteriol 72:445–459
65. Pearson L, Mihali T, Moffitt M, Kellmann R, Neilan B (2010) On the chemistry, toxicology
and genetics of the cyanobacterial toxins, microcystin, nodularin, saxitoxin and cylindrospermopsin. Mar Drugs 8:1650–1680
66. Babica P, Bláha L, Maršálek B (2006) Exploring the natural role of microcystins – a review of
effects on photoautotrophic organisms. J Phycol 42:9–20
67. Leflaive JP, Ten-Hage L (2007) Algal and cyanobacterial secondary metabolites in freshwaters: a comparison of allelopathic compounds and toxins. Freshw Biol 52:199–214
68. Li Y, Li D (2012) Competition between toxic Microcystis aeruginosa and nontoxic
Microcystis wesenbergii with Anabaena PCC7120. J Appl Phycol 24:69–78
69. Mazmouz R, Chapuis-Hugon F, Pichon V, Méjean A, Ploux O (2011) The last step of the
biosynthesis of the cyanotoxins cylindrospermopsin and 7-epi-cylindrospermopsin is
catalysed by CyrI, a 2-Oxoglutarate-dependent iron oxygenase. Chembiochem 12:858–862
70. Burford MA, Beardall J, Willis A, Orr PT, Magalhaes VF, Rangel LM, Azevedo SMFOE,
Neilan BA (2016) Understanding the winning strategies used by the bloom-forming cyanobacterium Cylindrospermopsis raciborskii. Harmful Algae 54:44–53
71. Preussel K, Wessel G, Fastner J, Chorus I (2009) Response of cylindrospermopsin production
and release in Aphanizomenon flos-aquae (Cyanobacteria) to varying light and temperature
conditions. Harmful Algae 8:645–650
72. Rzymski P, Poniedziałek B, Kokociński M, Jurczak T, Lipski D, Wiktorowicz K (2014)
Interspecific allelopathy in cyanobacteria: Cylindrospermopsin and Cylindrospermopsis
raciborskii effect on the growth and metabolism of Microcystis aeruginosa. Harmful Algae
35:1–8
73. Sant’Anna CL, de Carvalho LR, Fiore MF, Silva-Stenico ME, Lorenzi AS, Rios FR, Konno K,
Garcia C, Lagos N (2011) Highly toxic Microcystis aeruginosa strain, isolated from São Paulo
– Brazil, produce hepatotoxins and paralytic shellfish poison neurotoxins. Neurotox Res
19:389–402
74. Legrand C, Rengefkors K, Fistarol G, Granéli E (2003) Allelopathy in phytoplankton –
biochemical, ecological and evolutionary aspects. Phycologia 42:406–419
75. Matsuura HN, Fett-Neto AG (2017) Plant alkaloids: main features, toxicity, and mechanisms
of action. In: Carlini CR, Ligabue-Braun R (eds) Plant toxins. Springer Netherlands, Dordrecht
76. Wink M, Twardowski T (1992) Allelochemical properties of alkaloids. Effects on plants,
bacteria and protein biosynthesis. In: Rizvi SJH, Rizvi V (eds) Allelopathy: basic and applied
aspects. Springer Netherlands, Dordrecht
77. Pattanaik B, Lindberg P (2015) Terpenoids and their biosynthesis in cyanobacteria. Life
5:269–293
14 Effects of Cyanobacterial Secondary Metabolites on Phytoplankton Community. . . 341
Antimicrobial activity of the cyanobacteria Anabaena wisconsinense and Oscillatoria
curviceps against pathogens of fish in aquaculture. Ann Microbiol 58:527–534
60. Jonas A, Buranova V, Scholz S, Fetter E, Novakova K, Kohoutek J, Hilscherova K (2014)
Retinoid-like activity and teratogenic effects of cyanobacterial exudates. Aquat Toxicol
155:283–290
61. Jonas A, Scholz S, Fetter E, Sychrova E, Novakova K, Ortmann J, Benisek M, Adamovsky O,
Giesy JP, Hilscherova K (2015) Endocrine, teratogenic and neurotoxic effects of cyanobacteria
detected by cellular in vitro and zebrafish embryos assays. Chemosphere 120:321–327
62. Zagatto PA, Buratini S, Aragão MA, Ferrão-Filho AS (2012) Neurotoxicity of two Cylindrospermopsis raciborskii (cyanobacteria) strains to mice, Daphnia, and fish. Environ Toxicol
Chem 31:857–862
63. Otten TG, Paerl HW (2015) Health effects of toxic cyanobacteria in U.S. drinking and
recreational waters: our current understanding and proposed direction. Curr Environ Health
Rep 2:75–84
64. Carmichael WW (1992) Cyanobacteria secondary metabolites – the cyanotoxins. J Appl
Bacteriol 72:445–459
65. Pearson L, Mihali T, Moffitt M, Kellmann R, Neilan B (2010) On the chemistry, toxicology
and genetics of the cyanobacterial toxins, microcystin, nodularin, saxitoxin and cylindrospermopsin. Mar Drugs 8:1650–1680
66. Babica P, Bláha L, Maršálek B (2006) Exploring the natural role of microcystins – a review of
effects on photoautotrophic organisms. J Phycol 42:9–20
67. Leflaive JP, Ten-Hage L (2007) Algal and cyanobacterial secondary metabolites in freshwaters: a comparison of allelopathic compounds and toxins. Freshw Biol 52:199–214
68. Li Y, Li D (2012) Competition between toxic Microcystis aeruginosa and nontoxic
Microcystis wesenbergii with Anabaena PCC7120. J Appl Phycol 24:69–78
69. Mazmouz R, Chapuis-Hugon F, Pichon V, Méjean A, Ploux O (2011) The last step of the
biosynthesis of the cyanotoxins cylindrospermopsin and 7-epi-cylindrospermopsin is
catalysed by CyrI, a 2-Oxoglutarate-dependent iron oxygenase. Chembiochem 12:858–862
70. Burford MA, Beardall J, Willis A, Orr PT, Magalhaes VF, Rangel LM, Azevedo SMFOE,
Neilan BA (2016) Understanding the winning strategies used by the bloom-forming cyanobacterium Cylindrospermopsis raciborskii. Harmful Algae 54:44–53
71. Preussel K, Wessel G, Fastner J, Chorus I (2009) Response of cylindrospermopsin production
and release in Aphanizomenon flos-aquae (Cyanobacteria) to varying light and temperature
conditions. Harmful Algae 8:645–650
72. Rzymski P, Poniedziałek B, Kokociński M, Jurczak T, Lipski D, Wiktorowicz K (2014)
Interspecific allelopathy in cyanobacteria: Cylindrospermopsin and Cylindrospermopsis
raciborskii effect on the growth and metabolism of Microcystis aeruginosa. Harmful Algae
35:1–8
73. Sant’Anna CL, de Carvalho LR, Fiore MF, Silva-Stenico ME, Lorenzi AS, Rios FR, Konno K,
Garcia C, Lagos N (2011) Highly toxic Microcystis aeruginosa strain, isolated from São Paulo
– Brazil, produce hepatotoxins and paralytic shellfish poison neurotoxins. Neurotox Res
19:389–402
74. Legrand C, Rengefkors K, Fistarol G, Granéli E (2003) Allelopathy in phytoplankton –
biochemical, ecological and evolutionary aspects. Phycologia 42:406–419
75. Matsuura HN, Fett-Neto AG (2017) Plant alkaloids: main features, toxicity, and mechanisms
of action. In: Carlini CR, Ligabue-Braun R (eds) Plant toxins. Springer Netherlands, Dordrecht
76. Wink M, Twardowski T (1992) Allelochemical properties of alkaloids. Effects on plants,
bacteria and protein biosynthesis. In: Rizvi SJH, Rizvi V (eds) Allelopathy: basic and applied
aspects. Springer Netherlands, Dordrecht
77. Pattanaik B, Lindberg P (2015) Terpenoids and their biosynthesis in cyanobacteria. Life
5:269–293
14 Effects of Cyanobacterial Secondary Metabolites on Phytoplankton Community. . . 341