Abstract
We examined the growth of testate amoebae preying on Microcystis whose physiological states were different in laboratory experiments and a hypertrophic pond. We prepared three experimental systems using water samples dominated by Microcystis aeruginosa: light incubation (control), dark incubation (dark), and light incubation with addition of nitrogen and phosphorus (+NP). In all the systems, the colony density of M. aeruginosa decreased slightly during incubation. Physiological activity of phytoplankton as determined by chlorophyll fluorescence was high and almost constant in the control and +NP systems, whereas it decreased in the dark system. Cell densities of testate amoebae increased in the control and +NP systems, whereas in the dark system they remained low. Thus, growth of the amoebae was low in the systems where physiological activity of Microcystis was low. In a hypertrophic pond, cell density of testate amoebae increased and remained high when M. aeruginosa predominated. Cell density of testate amoebae increased remarkably, simultaneously with the increases in M. aeruginosa colony density and phytoplankton physiological activity. We also found a significant correlation between densities of M. aeruginosa colonies and testate amoebae. We suggested that the physiological activity of Microcystis is one important factor affecting the growth of testate amoebae grazing on Microcystis.



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Becares E, Romo S (1994) Selective predation of Thecamoeba sphaeronucleolus (Greeff, 1891) on filamentous algae in natural conditions. J Gen Appl Microbiol 40:15–21
Cole GT, Wynne MJ (1974) Endocytosis of Microcystis aeruginosa by Ochromonas danica. J Phycol 10:397–410
Cook WL, Ahearn DG, Reinhardt DJ, Reiber RJ (1974) Blooms of an algophorous amoeba associated with Anabeba in a freshwater lake. Water Air Soil Pollut 3:71–80
Dryden RC, Wright SJL (1987) Predation of cyanobacteria by protozoa. Can J Microbiol 33:471–482
Fulton RS, Paerl HW (1987) Toxic and inhibitory effects of the blue-green alga Microcystis aeruginosa on herbivorous zooplankton. J Plankton Res 9:837–855
Hanazato T, Yasuno M (1984) Growth, reproduction and assimilation of Moina macrocopa fed on Microcystis and/or Chlorella. Jpn J Limnol 34:195–202
Harris GP (1978) Photosynthesis, productivity and growth: the physiological ecology of phytoplankton. Arch Hydrobiol Beih Ergeb Limnol 10:1–177
Ho TS, Alexander M (1974) The feeding of amoebae on the filamentous blue-green algae. Bot Bull Acad Sin 23:63–70
Jarvis AC, Hart RC, Combrink S (1987) Zooplankton feeding on size fractionated Microcystis colonies and Chlorella in a hypertrophic lake (Hartbeespoort Dam, South Africa): implications to resource utilization and zooplankton succession. J Plankton Res 9:1231–1249
Kawanabe H, Mizuno T (1989) Freshwater fishes in Japan. Yama-to-Keikoku-sha Co. Ltd, Tokyo
Kim BR, Nakano S, Kim BH, Han MS (2006) Growth and grazing of the heterotrophic nanoflagellate, Diphylleia rotans on the cyanobacterium Microcystis aeruginosa. Aquat Microb Ecol 45:163–170
Laybourn-Parry J, Jones K, Holdich JP (1987) Grazing by Mayorella sp. (Protozoa: Sarcodina) on cyanobacteria. Funct Ecol 1:99–104
Liu X, Shi M, Liao Y, Gao Y, Zhang Z, Wen D (2006) Feeding characteristics of an amoeba (Lobosea: Naegleria) grazing upon cyanobacteria: food selection, ingestion and digestion progress. Microb Ecol 51:315–325
Manage PM, Kawabata Z, Nakano S (1999) Seasonal changes in densities of cyanophage infectious to Microcystis aeruginosa in a hypereutrophic pond. Hydrobiologia 411:211–216
Manage PM, Kawabata Z, Nakano S (2001) Dynamics of cyanophages and algicidal bacteria causing Microcystis aeruginosa mortality. Limnology 2:73–78
Miura T (1990) The effects of planktivorous fishes on the plankton community in a eutrophic lake. Hydrobiologia 200(210):567–579
Moran R, Porath D (1980) Chlorophyll determination in intact tissues using N,N-dimethylformamide. Plant Physiol 65:478–479
Moriarty DJW (1973) The physiology of digestion of blue-green algae in the cichlid fish, Tilapia nilotica. J Zool 171:25–39
Nakano S, Ishii N, Manage PM, Kawabata Z (1998) Trophic roles of heterotrophic nanoflagellates and ciliates among planktonic organisms in a hypereutrophic pond. Aquat Microb Ecol 16:153–161
Nakano S, Hayakawa K, Frenette JJ, Nakajima T, Jiao C, Tsujimura S, Kumagai M (2001a) Cyanobacterial blooms in a shallow lake: a large-scale enclosure assay of the importance of diurnal stratification. Arch Hydrobiol 150:491–509
Nakano S, Manage PM, Nishibe Y, Kawabata Z (2001b) Trophic linkage among heterotrophic nanoflagellates, ciliates and metazoan zooplankton in a hypereutrophic pond. Aquat Microb Ecol 25:259–270
Nishibe Y, Kawabata Z, Nakano S (2002) Grazing on Microcystis aeruginosa by the heterotrophic flagellate Collodictyon triciliatum in a hypertrophic pond. Aquat Microb Ecol 29:173–179
Nishibe Y, Manage PM, Kawabata Z, Nakano S (2004) Trophic coupling of testate amoeba and Microcystis species in a hypertrophic pond. Limnology 5:71–76
Nishii K, Nakano S, Tamada M, Manage PM, Nishibe S, Kawabata Z (2001) Microbial decomposition of dissolved organic matter in a hypertrophic pond. Limnology 2:207–212
Oliver RL, Ganf GC (2000) Freshwater blooms. In: Whitton BA, Potts M (eds) Ecology of cyanobacteria: their diversity in time and space. Kluwer, Dordrecht, pp 149–194
Reynolds CS, Jaworski GHM, Cmiench HA, Leedale GF (1981) On the annual cycle of the blue-green alga Microcystis aeruginosa Kutz. emend. Elenkin. Philos Trans R Soc Lond Ser B 293:419–477
Rodriguez-Zaragoza S (1994) Ecology of free-living amoebae. Crit Rev Microbiol 20:225–241
Snell TW (1980) Blue-green algae and selection in rotifer populations. Oecologia 46:343–346
Whitton BA (1973) Interactions with other organism. In: Carr NG, Whitton BA (eds) The biology of blue-green algae. Blackwell, Oxford, pp 415–433
Wilken S, Wiezer S, Huisman J, Van Donk E (2010) Microcystins do not provide anti-herbivore defence against mixotrophic flagellates. Aquat Microb Ecol 59:207–216
Yamamoto Y (1981) Observation on the occurrence of microbial agents which cause lysis of blue-green algae in Lake Kasumigaura. Jap J Limnol 42:20–27
Yamamoto Y, Suzuki K (1984) Light and electron microscope observations and prey specificities of an algophorous amoeba from Japanese freshwater. J Gen Appl Microbiol 31:411–417
Zhang X, Watanabe MM, Inouye I (1996) Light and electron microscopy of grazing by Poterioochromonas malhamensis (Chrysophyceae) on a range of phytoplankton taxa. J Phycol 32:486–492
Acknowledgments
We thank Dr. Kotaro Takayama, Ehime University, for teaching us the PAM technique. Thanks are also due to the members of LAFWEDY, Ehime University, for their advice, discussions and encouragement throughout the study. We thank Dr. M.J. Morris for correction of our English and constructive comments on the manuscript. This study was partly supported by the Center of Excellence (COE) Program at the “Global Center of Excellence for Interdisciplinary Studies on Environmental Chemistry” by the Espec Foundation for Global Environment Research and Technology and by the Environment Research and Technology Development Fund (D-0905) of the Ministry of Environment, Japan.
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Mizuta, S., Imai, H., Chang, KH. et al. Grazing on Microcystis (Cyanophyceae) by testate amoebae with special reference to cyanobacterial abundance and physiological state. Limnology 12, 205–211 (2011). https://doi.org/10.1007/s10201-010-0341-1
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DOI: https://doi.org/10.1007/s10201-010-0341-1


