Grazing on Microcystis (Cyanophyceae) by testate amoebae with special reference to cyanobacterial abundance and physiological state

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

Feeding habits of omnivorous Asplanchna: comparison of diet composition among Asplanchna herricki, A. priodonta and A. girodi in pond ecosystems

Spatial distribution and the diet composition of Asplanchna species were studied in 18 water bodies in Matsuyama, Japan. The abundance of Asplanchna and other rotifers, crustaceans, phytoplankton and microbial plankton, together with basic environmental parameters, were determined between October and December 2006, and the distribution and diet composition of Asplanchna species were estimated. Three species of Asplanchna, A. herricki, A. priodonta and A. girodi were found in the present study, but A. herricki was rather less abundant than the other two species. Their diet composition was different among the species, showing that A. herricki consumed only particulate matter while the diet of A. priodonta included mainly phytoplankton, dominated by dinoflagellates. In contrast, A. girodi was rather carnivorous, and included other rotifers in its diet. Their different food habits are not explained by their morphotypes and trophi structures, suggesting this difference might be related to their feeding abilities. For A. girodi, prey selectivity (Chesson's α) for rotifer prey was negative, except for Keratella cochlearis. The amount of rotifers consumed was also low at a mean prey number of less than 3 per A. girodi gut. The result suggests that the predation impact of Asplanchna as a top-down controller of rotifer populations is species-specific and can be apparent only when Asplanchna population reaches high density in these ponds. From the present results, three Asplanchna species were found to belong to basically different feeding groups, A. herricki is detritivore while A. priodonta and A. girodi are omnivores; but A. girodi is more predacious

Lack of congruence in species diversity indices and community structures of planktonic groups based on local environmental factors.

The importance of analyzing the determinants of biodiversity and community composition by using multiple trophic levels is well recognized; however, relevant data are lacking. In the present study, we investigated variations in species diversity indices and community structures of the plankton taxonomic groups-zooplankton, rotifers, ciliates, and phytoplankton-under a range of local environmental factors in pond ecosystems. For each planktonic group, we estimated the species diversity index by using linear models and analyzed the community structure by using canonical correspondence analysis. We showed that the species diversity indices and community structures varied among the planktonic groups and according to local environmental factors. The observed lack of congruence among the planktonic groups may have been caused by niche competition between groups with similar trophic guilds or by weak trophic interactions. Our findings highlight the difficulty of predicting total biodiversity within a system, based upon a single taxonomic group. Thus, to conserve the biodiversity of an ecosystem, it is crucial to consider variations in species diversity indices and community structures of different taxonomic groups, under a range of local conditions

Canonical correspondence analysis results for whole zooplankton and plankton taxonomic groups.

<p>Graph showing canonical correspondence analysis results for whole zooplankton (a) and plankton taxonomic groups, namely, cladocerans (b), rotifers (c), ciliates (d), and phytoplankton (e). TP, total phosphorus; DOC, dissolved organic carbon in water; Chl, chlorophyll <i>a</i>; HNF, heterotrophic nanoflagellates. Each numbered point indicates an individual site.</p

Pair plot for genus richness of plankton taxonomic groups and whole zooplankton.

<p>The pair plots showing genus richness of the plankton taxonomic groups, namely, cladocerans, rotifers, ciliates, and phytoplankton, and whole zooplankton. Each point represents a single pond (<i>n</i> = 18). The numbers in the upper right-hand columns denote Pearson’s correlation coefficients.</p

Grazing on Microcystis (Cyanophyceae) by testate amoebae with special reference to cyanobacterial abundance and physiological state

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