Comparative population growth and life table demography of the rotifer Asplanchna girodi at different prey (Brachionus calyciflorus and Brachionus havanaensis) (Rotifera) densities

Population growth and life table demography of the predatory rotifer A. girodi using spineless Brachionus calyciflorus and spined Brachionus havanaensis as prey at densities of 1, 2, 4 and 8 ind. ml^–1 at 25°C were studied. Regardless of the prey species, the population of A. girodi increased with increasing availability of Brachionus in the medium. At any given prey density, A. girodi fed B. calyciflorus showed consistently better growth than when fed B. havanaensis. The maximum population densities of A. girodi varied from 0.28 to 1.8 ind. ml^–1 depending on the prey species and the density. The rate of population increase observed in population growth studies varied from 0.17 to 0.43 day^–1 when fed B. calyciflorus and 0.09 to 0.27 day^–1 when fed B. havanaensis. Male population of A. girodi was closely related to female density. The lowest average lifespan was observed for A. girodi when fed B. havanaensis at 1 ind. ml^–1, while the converse was the case when fed B. calyciflorus at comparable prey concentration. Net reproductive rates varied from 16 to 26 offspring female^–1 lifespan^–1 depending on the prey species and concentration. Generation time of A. girodi decreased with increasing food concentrations for both the prey species. The rates of population increase obtained from life table demography were lower for A. girodi when fed B. havanaensis than when fed B. calyciflorus.     

Feeding the fairy shrimp Streptocephalus (Anostraca - Crustacea) with the rotifer Anuraeopsis

Laboratory-cultured Streptocephalus torvicornis were offered 8 concentrations (from 6 to 800 ind. ml^–1) of Anuraeopsis fissa for periods of 2 h 30 min. Two size classes, small (male: 14.7 mm± 1.6, female: 15.4 mm± 1.3) and large (male: 20.0 mm±2.0, female: 23.1 mm± 1.5), of S. torvicornis were used. Functional response for large S. torvicornis (both sexes) plateaued at 400 rotifers ml^–1, while in small specimens it did so at 200 prey ml^–1. Females consumed significantly more (30%) prey than males. Large males consumed maximum 4730 rotifers h^–1, females 6560 h^–1.     

Lifetable demography of four cladoceran species in relation to algal food (Chlorella vulgaris) density

Algal food density is known to influence life history variables of cladoceran species. It is not, however, well established whether both littoral and planktonic cladocerans show similar trends when exposed to increasing food concentrations. In the present work, we studied the life table demography of four cladoceran species (Ceriodaphnia cornuta, Moina macrocopa, Pleuroxus aduncus and Simocephalus vetulus) in relation to three algal food concentrations (low: 0.5 × 10⁶, medium: 1.5 × 10⁶ and high: 4.5 × 10⁶ cells ml^–1 of Chlorella vulgaris) (in terms of carbon content, these were equivalent to 0.15, 0.45 and 1.35 g ml^–1, respectively) at 25 °C. In general, for all the tested cladoceran species, values of average lifespan, gross reproductive rate, net reproductive rate, generation time and the rate of population growth were higher at lower food concentrations. Furthermore, high food concentration resulted in a negative population growth rate (mean ± standard error: –0.091 ± 0.026) for P. aduncus. The highest population growth rate (0.602 ± 0.014) was recorded for M. macrocopa at low food density. S. vetulus had the longest average lifespan (40 ± 1 d) while M. macrocopa had the lowest (5 ± 1 d). C. cornuta showed better performance at medium food concentration. We conclude that among the algal concentrations used here, 0.5 × 10⁶ – 1.5 × 10⁶ was beneficial not only to the planktonic species but also to the littoral P. aduncus and S. vetulus while 4.5 × 10⁶ cells ml^–1 was unsuitable for all the cladocerans tested.     

Population growth of some genera of cladocerans (Cladocera) in relation to algal food (Chlorella vulgaris) levels

We studied the patterns of population growth of 7 cladoceran species (Alona rectangula, Ceriodaphnia dubia, Daphnia laevis, Diaphanosoma brachyurum, Moina macrocopa, Scapholeberis kingi and Simocephalus vetulus) using 6 algal densities, viz. 0.05×10⁶, 0.1×10⁶, 0.2×10⁶, 0.4×10⁶, 0.8×10⁶ and 1.6×10⁶ cells ml^–1, of Chlorella vulgaris for 18 – 30 days. In terms of carbon content these algal concentrations corresponded to 0.29, 0.58, 1.16, 2.33, 4.65 and 9.31 g ml^–1, respectively. Cladocerans in the tested range of algal levels responded similarly, in that increasing the food concentrations resulted in higher numerical abundance and population growth rates (r). The peak population densities were (mean±standard error) 71±5; 17.1±0.4, 3.6±0.3, 12.7±1.1, 18.2±2.7, 15.8±1.0 and 10.9±0.02 ind. ml^–1, respectively for A. rectangula, C. dubia, D. laevis, D. brachyurum, M. macrocopa, S. kingi and S. vetulus. In general, the lowest r values were obtained for D. laevis (0.01±0.001) at 0.05×10⁶ cells ml^–1 food level while the highest was 0.283±0.004 for A. rectangula at 1.6×10⁶ cells ml^–1 of Chlorella. When the data of peak population density for each cladoceran species were plotted against the body length, we found an inverse relation, broadly curvilinear in shape. From regression equations between the food level and rate of population increase, we calculated the theoretical food quantity (the threshold level) required to maintain a zero population growth (r = 0) for each cladoceran species, which varied from 0.107 to 0.289 g ml^–1 d^–1 depending on the body size. When we plotted the cladoceran body size against the corresponding threshold food levels, we obtained a normal distribution curve. From this it became evident that for up to 1300 m body size, the threshold food level increased with increasing body size; however, beyond this, the threshold level decreased supporting earlier observations on rotifers and large cladocerans.     

Utilization of cyanobacteria by Brachionus calyciflorus: Anabaena flos-aquae (NRC-44-1) as a sole or complementary food source

The rotifer Brachionus calyciflorus can utilize the cyanobacterium Anabaena flos-aquae as either a sole or supplementary food source in laboratory culture. Positive population growth rates accompany food densities of 10 or 100 µg dry weight ml^–1, but slightly negative rates are found at a lower density (1.0 µg ml^–1). These results are consistent for rotifers feeding on two strains of A. flos-aquae, UTEX-1444 and NRC-44-1, with slightly enhanced survivorship and reproduction with the latter food. A 1:1 mixture (by dry weight) of Euglena gracilis and A. flos-aquae (NRC-44-1) produces survivorship comparable to that of control rotifer cohorts fed E. gracilis alone, but elicits significantly greater fecundity and population growth rates than found with the control food suspension at the same biomass density.     

Effect of Aeolosoma sp. (Aphanoneura: Aeolosomatidae) on the Population Dynamics of Selected Cladoceran Species

Although oligochaete worms naturally coexist with cladocerans in many shallow freshwater ponds and lakes, their influence on the latter is not well established. In this work we studied the effect of Aeolosoma sp. on the population growth of Alona rectangula, Ceriodaphnia dubia, Daphnia pulex, Macrothrix triserialis and Moina macrocopa. Population growth studies were conducted at one algal food density (1 × 10⁶cells ml^–1 of Chlorella vulgaris). The experimental design was similar for all five cladoceran species, where we used 100 ml capacity transparent jars containing 50 ml of EPA medium with the desired algal density and three replicates for each treatment. The test medium was changed daily and fresh algal food was added. The initial density of each of the cladoceran species in the population growth studies was 0.4 ind ml^–1 while that of the worms 1.0 ind ml^–1. Following inoculation, we estimated daily the number of cladocerans and the worms for duration of 21 days. Regardless of the presence of worms, Moina macrocopa and Macrothrix triserialis showed rapid population growth while A. rectangula took more than 2 weeks to reach peak abundances. With the exception of M. triserialis, all the other our cladoceran species declined in the presence of Aeolosoma sp. The lowest peak population density (about 1 ind ml^–1) was observed for M. triserialisin controls. The remaining species had peak densities of about 3–5 ind ml^–1. The rates of population increase per day varied from 0.03 to 0.19 depending on the cladoceran taxa and the treatment. In general we found that pelagic taxa were more adversely affected by the presence of the worms than were the littoral cladocerans.     

Predatory and toxic effects of the turbellarian (Stenostomum cf leucops) on the population dynamics of Euchlanis dilatata,Plationus patulus (Rotifera) and Moina macrocopa (Cladocera)

Catenulid turbellarians, common in shallow, tropical ponds, affect their rotifer prey via the production of toxins. There is, however, no quantitative information on their effect on the demography of their prey. Here, we test the impact of Stenostomum cf leucops on the population dynamics of the rotifers Euchlanis dilatata and Plationus patulus, and the cladoceran Moina macrocopa. Experiments were initiated with rotifers at 0.5 ind. ml⁻¹ and the cladoceran at 0.2 ind. ml⁻¹; growth patterns were compared in the absence and presence of worms (2 Stenostomum ind. per 50 ml). Results revealed that brachionids were most adversely affected: there was a lower growth rate of the rotifers in the presence of worms (P < 0.01, repeated measures ANOVA), although at the densities applied, the predator did not wipe out its prey. These littoral predators may therefore regulate rotifer prey in natural conditions. In Moina, the population evolved differently; initially, we found no difference between control and treatment, but after about 10 days, the population collapsed, irrespective of a direct or indirect contact with the predator. This delayed effect deserves more study, as it could represent flatworm toxin accumulation by the cladoceran.     

Studies on functional response and prey selection using zooplankton in the anostracan Chirocephalus diaphanus Prevost, 1803

Freshwater cladocerans and rotifers were used as prey to study functional response and prey selection by adult females of Chirocephalus diaphanus under laboratory conditions. For functional response studies, we offered three rotifer species (Brachionus calyciflorus, B. patulus and Euchlanis dilatata) and three cladoceran species (Alona rectangula, Ceriodaphnia dubia and Moina macrocopa) at various densities ranging from 0.5 to 16 ind. ml^–1. We found increased zooplankton consumption with increasing prey density but beyond 4 ind ml^–1 cladocerans and 8 ind. ml^–1 rotifers, the number of animals eaten plateaued. In general, C. diaphanus consumed fewer large prey (cladocerans) and many more smaller zooplankton (rotifers). For prey selection experiments, we used B. calyciflrous, B. patulus, C. dubia and M. macrocopa, offered at the ratio of two rotifers: one cladoceran and at three prey densities (total zooplankton numbers: 3, 6 and 12 ind. ml^–1). Prey selectivity patterns followed the functional response trends. In general, regardless of prey types, with an increase in the available zooplankton, there was an increase in the number of prey consumed. At any given prey density, C. diaphanus consumed higher numbers of rotifers than cladocerans. Among the prey offered, B. patulus and M. macrocopa were positively selected. Results are discussed in light of possible control of zooplankton by anostracans in temporary ponds.     

Demographic parameters of Brachionus patulus Muller (Rotifera) exposed to sublethal DDT concentrations at low and high food levels

The combined effects of sublethal levels of DDT (0, 15, 30, 45, and 60 µg·l^–1) and food (Chlorella at 1 and 3 × 10⁶ cells ml^–1) on the demography of the rotifer Brachionus patulus were studied. The average lifespan, life expectancy, net reproductive rate (R_o) and intrinsic rate of increase (r) were significantly greater at the higher food level, but declined with increasing DDT concentration. A significant DDT food interaction was manifested in the toxicity-mitigating action of the higher food density at higher DDT levels. The r values were negative at DDT levels 30 µg · l^–1 and above, only when food density was low. The effective DDT concentration at which a given parameter value was reduced to 50% of that in the controls (EC50) was lower at lower food levels for both survivorship and reproduction, and lower for reproduction than for survivorship at either food level.     

Effect of salinity on competition between the rotifers Brachionus rotundiformis Tschugunoff and Hexarthra jenkinae (De Beauchamp) (Rotifera)

We studied the effect of different concentrations (0, 3, 6, 9 and 12 g l^–1) of sodium chloride at one food level of Chlorella (1×10⁶ cells ml^–1) on competition between the rotifers B. rotundiformis and H. jenkinae, both of which were isolated from a saline lake. The population growth experiments were conducted for 3 weeks. Both the rotifer species did not survive beyond one week at a salinity of 0 g l^–1. Regardless of salt concentration and the presence of a competitor, H. jenkinae reached higher densities than B. rotundiformis. When grown alone, both B. rotundiformis and H. jenkinae showed optimal peak population densities at the salinity of 6 and 9 g l^–1. Since biomass wise, B. rotundiformis was larger than H. jenkinae, it showed a lower numerical abundance. Thus, the maximum peak population densities of B. rotundiformis and H. jenkinae recorded in this study were 107±3 and 203±28 ind. ml^–1. The maximal rates of population increase for B. rotundiformis and H, jenkinae when grown alone were 0.264±0.003 and 0.274±0.004, respectively. Our results also indicated that B. rotundiformis and H. jenkinae coexisted better at a salinity of 6 and 9 g l^–1 of sodium chloride while a salinity of 3 g l^–1 favoured Hexarthra over B. rotundiformis. At 12 g l^–1, both the rotifer species grown alone or together showed lower growth rates compared to those at lower salinity levels. Except 0 g l^–1, in all other salinity treatments, H. jenkinae was a superior competitor to B. rotundiformis.     

The maintenance ofBdellovibrio at low prey density

A mathematical model for the interaction ofBdellovibrio and its prey predicted that a relatively high prey density (7×10⁵ cells ml^–1) would be required for the establishment of an equilibrium in a mixed population [8]. The present report shows thatBdellovibrio can be maintained in a continuous culture when the prey cell density is much lower (2–5×10⁴ cells ml^–1), and closer to that of naturally occurring bacterial populations in sea waters.     

Feeding preference and population growth of Asplanchna brightwelli (Rotifera) offered two non-evasive prey rotifers

Population growth rates of the predatory rotifer Asplanchna brightwelli were determined at 25 °C using a large (Brachionus calyciflorus) and a small (Anuraeopsis fissa) rotifer prey species in three concentrations (0.5, 0.1 and 2.0 g dry weight ml^-1) and in five combinations. The prey ingestion time by the predator was also measured. For B. calyciflorus the ingestion time (22.97–8.95 s) was more than six times that of A. fissa (3.68 ± 0.93). Regardless of prey type, the population growth of Asplanchna increased with increasing food density. There was a direct correlation between densities of amictic and mictic fernales. The maximum rate of population growth (1.01 ± 0.10 d^-1) was higher at high density of A. fissa prey than that at the same density of B. calyciflorus. Progressive increase of A. fissa density in the offered food combination resulted in a corresponding increase of the predator's number. Gut content analysis of A. brightwelli revealed that the number of prey ingested increased with increasing prey densities.     

Life History Characteristics of <Emphasis Type="Italic">Asplanchnopus multiceps</Emphasis> (Rotifera) Fed Rotifer and Cladoceran Prey

Members of rotifer family Asplanchnidae are important invertebrate predators in freshwater communities. Although a considerable amount of information exists on species of Asplanchna, relatively less is known about Asplanchnopus. We isolated Asplanchnopus multiceps from the littoral of a small river in the State of Hidalgo in Central Mexico and separated a clone in our cultures. The gut content analysis of some animals collected from the field revealed the presence of cladocerans and rotifers, and therefore we cultured A. multiceps on a food mixture comprising littoral rotifers and cladocerans. We conducted population growth experiments of A. multiceps using six prey types (cladocerans: Macrothrix triserialis, Alona rectangula and Pleuroxus aduncus; rotifers, Brachionus patulus, B. macracanthus and B. urceolaris). The prey species (A. rectangula and B. patulus) on which the highest growth rates were observed were used to test the life-table demographic patterns in A. multiceps. All experiments were conducted in 50 ml containers with 25 ml of the medium and at three food levels (0.5, 1.0 and 2.0 ind. ml⁻¹ for the cladocerans, and 2.0, 4.0 and 8.0 ind. ml⁻¹ for the rotifers) with four replicates at each treatment. The spines of M. triserialis and B. macracanthus were apparently effective deterrents against Asplanchnopus predation since both these diets resulted in low, and sometimes negative, growth rates of the predator. The average lifespan and net reproductive rate of A. multiceps ranged from 3.8 to 8.4 days and 2.6 to 12.2 ind. female⁻¹, respectively, on A. rectangula; and from 5.0 to 9.4 days and 1.6–18.4 ind. female⁻¹, respectively, on B. patulus. The rate of population increase of A. multiceps ranged from 0.1 to 0.8 d⁻¹, depending on the prey type and density. The role of A. multiceps in structuring littoral rotifer and cladoceran communities is discussed.     

Morphometric and demographic responses of brachionid prey (Brachionus calyciflorus Pallas and Plationus macracanthus (Daday)) in the presence of different densities of the predator Asplanchna brightwellii (Rotifera: Asplanchnidae)

We quantified the indirect effects of different densities (1, 4, 16 individuals per jar) of the predator Asplanchna brightwellii on the morphometry and demography of their prey Brachionus calyciflorus and Plationus macracanthus. Population growth and life table demography experiments were separately conducted for each of the two prey rotifer species while keeping A. brightwellii in indirect contact. The brachionids were fed the green alga Chlorella vulgaris at a density of 1 × 10⁶ cells ml⁻¹. As compared to those cultured in the absence of the predator, in the presence of A. brightwellii the postero-lateral spines of P. macracanthus increased by about 15 μm, while in B. calyciflorus the increase was more (>80 μm). For both the brachionid species, the peak population density significantly decreased in the presence of A. brightwellii. The reproductive variables viz., net reproductive rate, generation time, and the rate of population increase of B. calyciflorus and P. macracanthus were negatively affected in the presence of kairomones from A. brightwellii.     

Combined effects of food level and inoculation density on competition between Brachionus patulus (Rotifera) and the cladocerans Ceriodaphnia dubia and Moina macrocopa

Competition among cladocerans and rotifers is of considerable interest not only due to their close similarity in life history strategies, but also due to the considerable overlap they exhibit in their feeding habits. In tropical waterbodies, several genera of cladocerans, including Ceriodaphnia and Moina occur, simultaneously with rotifers. We tested over a period of 3 weeks the combined effects of food (0.5×10⁶ and 1.5×10⁶ cells ml^–1 of Chlorella) level and rotifer density on the competition between B. patulus and C. dubia and M. macrocopa using population growth experiments. For each cladoceran species we used 30 test jars of 50 ml capacity. The initial density of cladocerans was 0.2 ind ml^–1, while for B. patulus it was either 1 ind ml^–1 or 5 ind ml^–1. Neither the maximal population density nor the rate of population increase (r) of C. dubia was significantly affected by B. patulus. However, for M. macrocopa, both these variables were negatively affected by the rotifers. The combined effects of low food level and high initial density of B. patulus resulted in a 50% reduction in the peak population density of M. macrocopa. The population growth of B. patulus was negatively influenced by the presence of C. dubia and M. macrocopa. The results of the competition experiments conducted in the present study between cladocerans and rotifers suggest the existence of a more complex and delicate interaction than is generally thought.     

Ecological problems of Lake Ladoga: causes and solutions

We studied the outcome of competition between a large (Brachionus calyciflorus) and a small (Anuraeopsis fissa) rotifer species at five algal (Scenedesmus acutus) concentrations (0.5 × 10⁶ to 40.5 × 10⁶ cells ml^–1) and with varying initial densities in mixed populations (100 to 0% of B. calcyciflorus or A. fissa), the combined initial biomass being 0.2 µg ml^–1 in all test jars. Experiments were conducted at 28 ± 1 °C.Regardless of food concentration, B. calcyciflorus showed a greater increase in biomass than A. fissa, peak densities (mean ± standard error) at the lowest food concentration in the controls being 1.34 ± 0.31 µg dry weight ml^–1 and 0.82 ± 0.08 dry weight ml^–1, respectively. At the lower food concentrations, A. fissa displaced B. calyciflorus and vice versa at the higher food concentrations. At the intermediate food concentrations of 4.5 × 10⁶ cells ml^–1, B. calyciflorus outcompeted A. fissa only if its initial population density was three times higher. The rates of population growth in controls varied from 0.792 ± 0.06 d^–1 to 1.492 ± 0.13 d^–1 for B. calyciflorus and 0.445 ± 0.04 to 0.885 ± 0.01 for A. fissa depending on food level. When both species were introduced together, low food levels favoured higher abundance of A. fissa than B. calyciflorus, suggesting, in nature, it is likely that small Anuraeopsis colonize oligotrophic water bodies more successfully than larger Brachionus. The results also suggest that the outcome of competition depends not only on the size of the competing species and food availability but also on their colonizing density.     

Rotifers as predators on small ciliates

Clearance rates of Synchaeta pectinata, Brachionus calyciflorus and Asplanchna girodi on Tetrahymena pyriformis (46 µm in length) at a density of 10 cells ml^–1, in the presence of algal food, were 2.5 to 6.1 ml rot.^–1 day^–1. Clearance rates of these rotifers were, respectively, about 2, 3, and 13 times lower on Strobilidium gyrans (58 µm in length) than on T. pyriformis, indicating that the saltations of S. gyrans are an effective escape response. Clearance rates of S. pectinata were considerably lower on Colpidium striatum (81 µm) than on S. gyrans, suggesting that S. pectinata may not be able to ingest ciliates of this size. S. pectinata had a clearance rate of 19 ml rot.^–1 day^–1 on S. gyrans at a density of 1.2 cells ml^–1, in the absence of edible algal food. Rotifers may prey extensively on ciliates in natural plankton communities, ingesting 25 to 50 individuals in the 45–60 µm size range day^–1.     

A study of the freshwater rotifer Brachionus calyciflorus in Pekanbaru, Riau, Indonesia

Brachionus calyciflorus is one of freshwaterrotifers found in fish ponds in Pekanbaru, Riau,Indonesia. Its density varied depending on that ofphytoplankton. Maximum of 2.5 ×10³ ind. l^–1 was found in ponds fertilised with animal wastes.The fecundity and population growth of B.calyciflorus was studied. Results indicated that the fecundity of amictic females was higher thanthat of unfertilized mictic females. During their life span, amictic and mictic females produced29.7 and 12.5 eggs per female, respectively. In the mass culture of 500 ml media, the highestdensity of female and male rotifers was 975.8 and 9.6 ind. ml^–1, respectively. During 8 days cultureperiod, they also produced eggs as many as 124.2 ml^–1.Human and animal wastespromoted the growth of phytoplankton as food forrotifers in the pond. A laboratory study confirms this. The best growth of B. calyciflorus at a density of 109 ind. ml^–1 was found at 0.5 g l^–1 of humanexcreta. A high density of B. calyciflorus (542ind. ml^–1) was also found in semi-continuous culturewith chicken excreta.     

High density culture of the freshwater rotifer,Brachionus calyciflorus

The freshwater rotifer, Brachionus calyciflorus is one of the live food organisms used for the mass production of larval fish. In this study possibility of obtaining high density cultures of the freshwater rotifer B. calyciflorus were investigated. The two culture systems used differed in their air and dissolved oxygen supplies using three temperatures in each case: 24, 28 and 32 °C. Rotifers were batch-cultured using 5 l-vessels and fed with the freshwater Chlorella. The growth rate of rotifers significantly increased with an increase in temperature. The maximum density of the rotifers with air-supply at 24 °C, 6500 ind. ml^–1, was significantly lower than those cultured at 28 and 32 °C, i.e. 8600 and 8100 ind. ml^–1, respectively. Dissolved oxygen levels decreased with time and ranged from 0.8 to 1.4 mg l^–1 when the density of freshwater rotifer was the highest at each temperature. The highest density (19200 ind. ml^–1) of freshwater rotifer was obtained in cultures with a supply of oxygen at 28 °C. Densities of 13500 and 17200 ind. ml^–1 were found at 24 and 32 °C, respectively. Levels of NH₃-N increased with time and a dramatic increase of NH₃-N was observed at high temperatures. Levels of NH₃-N at 24, 28 and 32 °C were 13.2, 18.5 and 24.5 mg l^–1, respectively. These levels coincided with the highest rotifer density at each of the three temperatures. When rotifers were cultured with an oxygen-supply and pH was adjusted to 7, the maximum density of rotifer reached 33500 ind. ml^–1 at 32 °C . These results suggested that high density culture of freshwater rotifer, B. calyciflorus could be achieved under optimal conditions with DO value of exceeding 5 mg l^–1 and NH₃-N values of lower than 12.0 mg l^–1.     

Predator–prey interactions between a planktonic ciliate Strombidium sp. (Ciliophora, Oligotrichida) and the dinoflagellate Pfiesteria piscicida (Dinamoebiales, Pyrrophyta)

The functional response of a planktonic ciliate, Strombidium sp. feeding on the dinoflagellate Pfiesteria piscicida non-toxic zoospores (NTZ) was experimentally studied with four different prey concentrations (43–3153 cells ml⁻¹). Data from direct observations (NTZ inside individual Strombidium sp.) was used to calculate predator–prey specific ingestion and clearance rates. The ingestion rates varied between 0.68 and 14.26 NTZ ind⁻¹ h⁻¹, and with the predator–prey specific handling time of 2.83 min the U_max was 21.18 NTZ ind⁻¹ h⁻¹. The increase in the prey concentration between approximately 700 and 3000 NTZ ml⁻¹ did not increase the uptake of prey, and at the lowest Pfiesteria NTZ concentrations the feeding efficiency of Strombidium sp. was lowered, possibly indicating a situation of threshold feeding. When data from direct observations of ingested Pfiesteria NTZ were compared with values of total NTZ loss from the experimental water during the experiment, ingestion was found to represent only a fraction of the total NTZ loss in the presence of ciliates. This discrepancy was concluded to be due to other grazer related factors than actual ciliate grazing. The control of the initial growth of Pfiesteria community, in a pre-bloom situation, would require only a small ciliate abundance (less than 5 ml⁻¹), but when the Pfiesteria NTZ are scarce, relatively more ciliates are needed to limit the population growth of the dinoflagellate community because of the apparent feeding threshold. It is concluded that the formation of non-toxic P. piscicida blooms require periods of low grazing pressure or a means to escape grazing.