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Responses of rotifers and cladocerans to Microcystis aeruginosa (Cyanophyceae): A demographic study

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Abstract

The response of selected rotifers and cladocerans to Microcystis aeruginosa, offered as colonies and single cells, was compared to that on a diet of Chlorella vulgaris using the life table demography approach. The test zooplankton species were Simocephalus vetulus, Daphnia carinata, Moina macrocopa, Scapholeberis kingi, Ceriodaphnia cornuta, Brachionus calyciflorus and Hexarthra mira. To detect the development of resistance to toxins from Microcystis in zooplankton, in addition to the laboratory cultured strain of Ceriodaphnia cornuta, another strain of the same species was also used (designated as C. cornuta 2, this was collected from a pond containing Microcystis and cultured in the laboratory on Chlorella for a few weeks prior to experimentation). Experiments were conducted at 20 °C and 30 °C. Survivorship was high on Chlorella in most species but low on diets of Microcystis. Except for C. cornuta 2, S. kingi and S. vetulus, all other test species were adversely affected by Microcystis. The ability to utilise Microcystis improved at 30 °C in M. macrocopa, D. carinata and H. mira. The longest mean lifespan was recorded for C. cornuta 2 (25.3 ± 4.86 d) and the lowest for B. calyciflorus (0.58 ± 0.05 d). The highest net reproductive rate was observed for C. cornuta 1 (44.9 ± 4.88) and the longest generation time of 26.6 ± 2.13 d for S. vetulus. Among the cladocerans that showed positive values of population growth rate (r), M. macrocopa had the highest of 0.96 ± 0.04 per day.

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References

  • Arnold DE (1971) Ingestion, assimilation, survival and reproduction by Daphnia pulex fed seven species of blue-green algae. Limnol Oceanogr 16: 906–920

    Google Scholar 

  • Carmichael WW (1986) Alagal toxins. Adv Bot Res 12: 47–101

    Google Scholar 

  • Carpenter SR, Kitchell JF and Hodgson JR (1985) Cascading trophic interactions and lake productivity. BioScience 35: 634–639

    Google Scholar 

  • Dawidowicz P (1990) Effectiveness of phytoplankton control by large-bodied and small-bodied zooplankton. Hydrobiologia 200/201: 43–47

    Google Scholar 

  • De Bernardi R, Giusanni G and Pedretti EL (1981) The significance of blue-green algae as food for filter feeding zooplankton: Experimental studies on Daphnia spp. fed by Microcystis aeruginosa. Verh Internat Verein Limnol 21: 477–483

    Google Scholar 

  • De Bernardi R and Giussani G (1990) Are blue green algae a suitable food for zooplankton? An overview. Hydrobiologia 200/201: 29–41

    Google Scholar 

  • DeClerk S, De Meester L, Podoor N and Conde-Porcuna JM (1997) The relevance of size efficiency to biomanipulation theory: a field test under hypertrophic conditions. Hydrobiologia 360: 265–275

    Google Scholar 

  • DeMott RW and Dhawale S (1995) Inhibition from in-vitro protein phosphatase activity in three zooplankton species by microcystin-LR, a toxin from cyanobacteria. Arch Hydrobiol 134: 417–424

    Google Scholar 

  • DeMott WR and Kerfoot WC (1982) Competition among cladocerans: nature of the interaction between Bosmina and Daphnia. Ecology 63: 1949–1966

    Google Scholar 

  • DeMott WR and Moxter F (1991) Foraging on cyanobacteria by copepods: responses to chemical defenses and resource abundance. Ecology 72: 1820–1834

    Google Scholar 

  • DeMott WR, Zhang QX and Carmichael WW (1991) Effects of toxic cyanobacteria and purified toxins on the survival and feeding of a copepod and three species of Daphnia. Limnol Oceanogr 36: 1346–1357

    Google Scholar 

  • Fernando CH, Paggi JC and Rajapaksa R (1987) Daphnia in tropical lowlands. Mem Ist Ital Idrobiol 45: 107–141

    Google Scholar 

  • Fulton RS III and Paerl HW (1987) Effects of colonial morphology on zooplankton utilisation of algal resources during blue-green algal (Microcystis aeruginosa) blooms. Limnol Oceanogr 32: 634–644

    Google Scholar 

  • Fulton RS III and Paerl HW (1988) Effects of the blue-green algae Microcystis aeruginosa on zooplankton competitive relations. Oecologia 76: 383–389

    Google Scholar 

  • Gilbert JJ (1990) Differential effects of Anabaena affinis on cladocerans and rotifers: Mechanisms and implications. Ecology 71: 1727–1740

    Google Scholar 

  • Gilbert JJ (1996) Effect of temperature on the response of planktonic rotifers to a toxic cyanobacterium. Ecology 77: 1174–1180

    Google Scholar 

  • Gliwicz ZM (1990) Why do cladocerans fail to control algal blooms? Hydrobiologia 200/201: 83–97

    Google Scholar 

  • Gliwicz ZM and Siedlar E (1980) Food size limitation and algae interfering with food collection in Daphnia. Arch Hydrobiol 88: 155–177

    Google Scholar 

  • Gordo T, Lubián LM and Cañavate JP (1994) Influence of temperature on growth, reproduction and longevity of Moina salina Daday, 1888 (Cladocera, Moinidae). J Plankton Res 16: 1513–1523

    Google Scholar 

  • Gulati RD (1990) Structural and grazing responses of zooplankton community to biomanipulation of some Dutch water bodies. Hydrobiologia 200/201: 99–118

    Google Scholar 

  • Gulati RD and DeMott WR (1997) The role of food quality for zooplankton: remarks on the state-of-the-art, perspectives and priorities. Freshwater Biol 38: 753–768

    Google Scholar 

  • Hanazato T (1991) Interrelations between Microcystis and cladocera in the highly eutrophic Lake Kasumigaura, Japan. Int Rev ges Hydrobiol 76: 21–36

    Google Scholar 

  • Hanazato T and Yasuno M (1984) Evaluation of Microcystis as food for zooplankton in a eutrophic lake. Hydrobiologia 144: 251–260

    Google Scholar 

  • Hietala J, Laurén-Määttä C and Walls M (1997) Sensititvity of Daphnia to toxic cyanobacteria: effects of genotype and temperature. Freshw Biol 37: 299–306

    Google Scholar 

  • Holm NP and Shapiro J (1984) Examination of lipid reserves and the nutritional status of Daphnia pulex fed Aphanizomenon flosaquae. Limnol Oceanogr 29: 1137–1140

    Google Scholar 

  • Jungmann D and Benndorf J (1994) Toxicity to Daphnia of a compound extracted from laboratory and natural Microcystis spp., and the role of microcystins. Freshwater Biol 32: 13–20

    Google Scholar 

  • Kiviranta J, Sivonen K, Lahti K, Luukkainen R and Niemela SI (1991) Production and biodegradation of cyanobacterial toxins-a laboratory study. Arch Hydrobiol 121: 281–294

    Google Scholar 

  • Lampert W (1981a) Toxicity of the blue-green Microcystis aeruginosa: Effective defence mechanism against grazing pressure by Daphnia. Verh Internat Verein Limnol 21: 1436–1440

    Google Scholar 

  • Lampert W (1981b) Inhibitory and toxic effects of blue-green algae on Daphnia. Int Revue ges Hydrobiol 66: 285–298

    Google Scholar 

  • Lampert W (1987) Laboratory studies on zooplanktoncyanobacteria interactions. NZJ Mar Freshwater Res 21: 483–490

    Google Scholar 

  • Lee HW and Ban S (1999) Effect of crowding on growth and reproduction of Simocephalus vetulus O.F. Müller. Hydrobiologia 391: 135–145

    Google Scholar 

  • Lynch M (1980) Aphanizomenon blooms: alternate control and cultivation by Daphnia pulex. In: Kerfoot WD (ed.) Evolution and ecology of zooplankton communities. pp. 299–304. Hanover, Univ Press of New England

  • Meybeck M, Chapman D and Helmer R (eds.) (1989) Global freshwater quality: a final assessment. Blackwell Reference, Oxford, UK 306 pp

    Google Scholar 

  • Nandini S and Rao TR (1998) Somatic and population growth in selected cladoceran and rotifer species offered the cyanobacterium Microcystis aeruginosa as food. Aquatic Ecol 31: 283–298

    Google Scholar 

  • Nandini S and Sarma SSS (2000) Life table demography of four cladoceran species in relation to algal food (Chlorella vulgaris) density. Hydrobiologia (In press)

  • Nizan S, Dimentman C and Shilo M (1986) Acute toxic effect of the cyanobacterium Microcystis aeruginosa on Daphnia magna. Limnol Oceanogr 31: 497–502

    Google Scholar 

  • O'Brien WJ and De Noyelles, FJr (1974) Filtering rate of Ceriodaphnia reticulata in pond water of varying phytoplankton concentrations. Am Midl Nat 91: 509–512

    Google Scholar 

  • Paerl HW, Tucker CS (1995)Ecology of blue-green algae in aquaculture ponds. J World Aquaculture Soc 26: 109–131

    Google Scholar 

  • Paerl HW (1988) Nuisance phytoplankton blooms in coastal, estuarine and inland waters. Limnol Oceanogr 33: 823–847

    Google Scholar 

  • Pianka ER (1988) Evolutionary ecology Harper and Row Publishers Inc. 468 pp

  • Porter KG and Orcutt JD (1980) Nutritional adequacy, manageability, and toxicity as factors that determine food quality of green and blue-green algae for Daphnia. Am Soc Limnol Oceanogr Spec Symp 3: 268–281

    Google Scholar 

  • Reynolds CS (1984) The ecology of freshwater phytoplankton. Cambridge University Press, Cambridge, UK 384 pp.

    Google Scholar 

  • Saint-Jean L (1983) The zooplankton. In: JP Carmouze et al. (Eds.) Lake Chad. Monographiae Biologicae, pp 199–232

  • Sarma SSS and Rao TR (1991) The combined effects of food and temperature on the life history parameters of Brachionus patulus Muller (Rotifera). Int. Revue ges. Hydrobiol. 76: 225–239.

    Google Scholar 

  • Sevrin-Reyssac J and Pletikosic M (1990) Cyanobacteria in fish ponds. Aquaculture 88: 1–20

    Google Scholar 

  • Shapiro J, Forsberg B, Lamarra V, Lindmark G, Lynch M, Smeltzer E and Zoto G (1982) Experiments and experiences in biomanipulation: studies of ways to reduce algal abundance and eliminate blue-greens. Interim Rep No. 19 Limnol Res center Univ. of Minnesota, Minneapolis, 251pp

  • Smith AD and Gilbert JJ (1995) Relative susceptibilities of rotifers and cladocerans to Microcystis aeruginosa. Arch Hydrobiol 132: 309–336

    Google Scholar 

  • Sokal RR and Rohlf FJ (1981) Biometry (2nd ed). W.H. Freeman and Company, San Francisco. 859 pp

    Google Scholar 

  • Starkweather PL and Kellar PE (1987) Combined influences of particulate and dissolved factors in the toxicity of Microcystis aeruginosa (NRC-SS-17) to the rotifer Brachionus calyciflorus. Hydrobiologia 147: 375–378

    Google Scholar 

  • Thompson JM, Ferguson AJD and Reynolds CS (1982) Natural filtration rates of zooplankton in a closed system: the derivation of a community grazing index. J Plankton Res 4: 545–560

    Google Scholar 

  • Trimbee AM and Prepas EE (1987) Evaluation of total phosphorus as a predictor of the relative biomass of blue-green algae with emphasis on Alberta lakes. Can J Fish Aquat Sci 44: 1337–1342

    Google Scholar 

  • van Hannen EJ, Zwart G, van Agterveld MP, Gons HJ, Ebert J and Laanbroek HJ (1999) Changes in bacterial and eukaryotic community structure after mass lysis of filamentous cyanobacteria associated with viruses. Appl Environ Microbiol 65: 795–801

    PubMed  Google Scholar 

  • Watanabe MF, Park HD and Watanabe M (1994) Composition of Microcystis species and hepatopeptide toxins. Verh Internat Verein Limnol 25: 2226–2229

    Google Scholar 

  • Webster KE and Peters RH (1978) Some size-dependent inhibition of larger cladoceran filterers in filamentous suspensions. Limnol Oceanogr 23: 1238–1245

    Google Scholar 

  • Zafar AR (1986) Seasonality of phytoplankton in some South Indian lakes. Hydrobiologia 138: 177–187

    Google Scholar 

Download references

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  1. S. Nandini

    Present address: Ecología Acuática, Conservación y Mejoramiento del Ambiente, División de Investigación, Universidad Nacional Autónoma de México, Campus Iztacala, AP 314, CP 54000, Los Reyes, Tlalnepantla, Estado de México, México

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  1. Department of Zoology, University of Delhi, Delhi, 110 007, India

    S. Nandini

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Nandini, S. Responses of rotifers and cladocerans to Microcystis aeruginosa (Cyanophyceae): A demographic study. Aquatic Ecology 34, 227–242 (2000). https://doi.org/10.1023/A:1009986928706

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