Physiological comparison between colonial and unicellular forms of Microcystis aeruginosa Kütz. (Cyanobacteria)

REFERENCES

• Abelson J.N. & Simon M.I. 1988. Phycobiliproteins in cyanobacteria. In: Method in enzymology (Ed. by P. Lester & N.G. Alexander), p. 167. Kluwer Academic Publishers, Dordrecht.
   Google Scholar
• Amemiya Y. & Nakayama O. 1984. The chemical composition and metal adsorption capacity of the sheath materials isolated from Microcystis, Cyanobacteria. Japanese Journal of Limnology 45: 187–193.
   Google Scholar
• Aráoz R. & Häder D-P. 1997. Ultraviolet radiation induces both degradation and synthesis of phycobilisomes in Nostoc sp.: a spectroscopic and biochemical approach. FEMS Microbiology Ecology 23: 301–313.
   Web of Science ®Google Scholar
• Carmichael W.W. 1994. The toxins of cyanobacteria. Scientific American 1: 64–72.
   Google Scholar
• Cermeň O.P., Maraňón E., Rodríguez J. & Fernández E. 2005. Size dependence of coastal phytoplankton photosynthesis under vertical mixing conditions. Journal of Plankton Research 27: 473–483.
   Web of Science ®Google Scholar
• Dubois M., Giles K.A., Hamilton J.K., Rebers P.A. & Smith F. 1956. Colorimetric method of determination of sugars and related substances. Analytical Chemistry 28: 350–356.
   Web of Science ®Google Scholar
• Eloff J.N. 1981. Autecological studies on Microcystis. In: The water environment algal toxins and health (Ed. by W.W. Carmichael), pp. 71–96. Plenum Press, New York.
   Google Scholar
• Forni C., Telo F.R. & Caiola M.G. 1997. Comparative analysis of the polysaccharides produced by different species of Microcystis (Chroococcales, Cyanophyta). Phycologia 36: 181–185.
   Web of Science ®Google Scholar
• Genty B., Briantais J.M. & Baker N.R. 1989. The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochimica et Biophysica Acta 990: 87–92.
   Web of Science ®Google Scholar
• Henley W.J. 1993. Measurement and interpretation of photosynthetic light-response curves in alga in the context of photoinhibition and diel changes. Journal of Phycology 29: 729–739.
   Web of Science ®Google Scholar
• King D.L. 1970. The role of carbon in eutrophication. Journal of the Water Pollution Control Federation 42: 2035–2051.
   Web of Science ®Google Scholar
• Lancelot C., Mathot S. & Owens N.J.P. 1986. Modeling protein synthesis, a step to an accurate estimate of net primary production: Phaeocystis pouchetii colonies in Belgian coastal waters. Marine Ecology Progress Series 32: 193–202.
   Web of Science ®Google Scholar
• Li Y. & Gao K. 2004. Photosynthetic physiology and growth as a function of colony size in the cyanobacterium Nostoc sphaeroides. European Journal of Phycology 39: 9–15.
   Web of Science ®Google Scholar
• Masojídek J., Grobbelaar J.U., Pechar L. & Koblízek M. 2001. Photosystem electron transport rates and oxygen production in natural water blooms of freshwater cyanobacteria during a diel cycle. Journal of Plankton Research 23: 57–66.
   Web of Science ®Google Scholar
• Maxwell K. & Johnson G.N. 2000. Chlorophyll fluorescence-a practical guide. Journal of Experimental Botany 345: 659–668.
   Web of Science ®Google Scholar
• Oliver R.L. & Ganf G.G. 2000. Freshwater blooms. In: Ecology of cyanobacteria: their diversity in time and space (Ed. by B.A. Whitton & M. Potts), pp. 1–11. Kluwer Academic Publishers, Dordrecht.
   Google Scholar
• Otero A. & Vincenzini M. 2003. Extracellular polysaccharide synthesis by Nostoc strains as affected by N source and light intensity. Journal of Biotechnology 102: 143–152.
   PubMed Web of Science ®Google Scholar
• Paerl H.W. 1983. Partitioning of CO2 fixation in the colonial cyanobacterium Microcystis aeruginosa: mechanism promoting formation of surface scums. Applied and Environmental Microbiology 46: 252–259.
   PubMed Web of Science ®Google Scholar
• Paerl H.W. & Ustach J.F. 1982. Blue-green algal scums: an explanation for their occurrence during freshwater blooms. Limnology and Oceanography 23: 179–184.
   Google Scholar
• Qiu B. & Gao K. 2002. Effects of CO2 enrichment on the bloom-forming cyanobacterium Microcystis aeruginosa (Cyanophyceae): physiological responses and relationships with the availability of dissolved inorganic carbon. Journal of Phycology 38: 721–729.
   Web of Science ®Google Scholar
• Raps S., Wyman K., Siegelman H.W. & Falkowski P.G. 1983. Adaptation of the cyanobacterium Microcystis aeruginosa to light intensity. Plant Physiology 72: 829–832.
   PubMed Web of Science ®Google Scholar
• Reynolds C.S. & Walsby A.E. 1975. Water blooms. Biological Research 50: 437–481.
   Google Scholar
• Reynolds C.S., Jaworski G., Cmiech H. & Leedale G. 1981. On the annual cycle of the blue-green alga Microcystis aeruginosa Kütz. emend. Elenkin. Philosophical Transactions of the Royal Society of London B Biological Sciences 293: 419–477.
   Web of Science ®Google Scholar
• Reynolds C.S., Oliver R.L. & Walsby A.E. 1987. Cyanobacterial dominance: the role of buoyancy regulation in dynamic lake environments. New Zealand Journal of Marine and Freshwater Research 21: 379–390.
   Web of Science ®Google Scholar
• Rippka R., Deruelles J., Waterbury J.B., Herdman M. & Stanier R.Y. 1979. Generic assignments, strain histories and properties of pure cultures of cyanobacteria. Journal of General Microbiology 111: 1–61.
   Google Scholar
• Sathyendranathe S., Lazzara L. & Prieur L. 1987. Variations in the spectral values of specific absorption of phytoplankton. Limnology and Oceanography 32: 403–415.
   Web of Science ®Google Scholar
• Sedmak B. & Elerše K. 2006. Microcystins induce morphological and physiological changes in selected representative phytoplanktons. Microbial Ecology 51: 508–515.
   PubMed Web of Science ®Google Scholar
• Shapiro J. 1972. Blue-green algae: why they become dominant. Science 179: 382–384.
   Web of Science ®Google Scholar
• Shen H. & Song L. 2007. Comparative studies on physiological responses to phosphorus in two phenotypes of bloom-forming Microcystis. Hydrobiologia. (in press).
   Google Scholar
• Sivonen K. 1996. Cyanobacterial toxins and toxin production. Phycologia 35: 12–24.
   Google Scholar
• Song L., Lei L., Ou D. & Gan N. 2004. Growth, photosynthetic affinity and toxicity of single-celled and colony-shaped Microcystis viridis. In: Harmful algae management and mitigation (Ed. by M.S. Hall, S. Etheridge, D. Anderson, J. Kleindinst, M. Zhu & Y. Zou), pp. 212–215. Asia-Pacific Economic Cooperation, Singapore.
   Google Scholar
• Tien C.J., Krivtsov V., Levado E., Sigee D.C. & White K.N. 2002. occurrence of cell-associated mucilage and soluble extracellular polysaccharides in Rostherne Mere and their possible significance. Hydrobiologia 485: 245–252.
   Web of Science ®Google Scholar
• Tilzer M.M. 1987. Light-dependence of photosynthesis and growth in cyanobacteria: implications for their dominance in eutrophic lakes. New Zealand Journal of Marine Freshwater Research 21: 401–412.
   Web of Science ®Google Scholar
• Wu Z., Gan N., Huang Q. & Song L. 2007. Response of Microcystis to copper stress — do phenotypes of Microcystis make a difference in stress tolerance? Environmental Pollution 147: 324–330.
   PubMed Web of Science ®Google Scholar
• Yamamoto Y. & Nakahara H. 2005a. The formation and degradation of cyanobacterium Aphanizomenon flos-aquae blooms: the importance of pH, water temperature, and day length. Limnology 6: 1–6.
   Web of Science ®Google Scholar
• Yamamoto Y. & Nakahara H. 2005b. Competitive dominance of the cyanobacterium Microcystis aeruginosa in nutrient-rich culture conditions with special reference to dissolved inorganic carbon uptake. Phycological Research 53: 201–208.
   Web of Science ®Google Scholar
• Zohary T. 1985. Hyperscums of the cyanobacterium Microcystis aeruginosa in a hypertrophic lake (Hartbeespoort Dam South Africa). Journal of Plankton Research 7: 399–409.
   Web of Science ®Google Scholar