Phagotrophic Mechanisms and Prey Selection in Free-living Dinoflagellates1

Three types of feeding mechanisms are known in dinoflagellates: pallium feeding, tube feeding, and direct engulfment. Pallium feeding has only been described for heterotrophic thecate species (Protoperidinium, Diplopsalis group). Tube feeding is commonly found among both naked and thecate species of mixotrophic and heterotrophic dinoflagellates (e.g. Amphidinium, Dinophysis, Gyrodinium, Peridiniopsis). Direct engulfment is mainly found among naked species (e.g. Gymnodinium, Gyrodinium, Noctiluca): recently, however, some thecate species have been shown to use this feeding mechanism as well. Feeding behavior in dinoflagellates involves several steps prior to actual ingestion, including precapture, capture, and prey manipulation. As feeding mechanisms allow the ingestion of relatively large prey or parts thereof, dinoflagellates are regarded as raptorial feeders. While prey size plays an important role in the ability of dinoflagellates to ingest food, this alone cannot explain observed prey preferences. Some dinoflagellate species can be very selective in their choice of prey, while others show a remarkable versatility.     

Cyclopoids feed selectively on free-living stages of parasites

1. Many aquatic organisms can consume parasite larvae, thus hampering parasite transmission; however, information about feeding on them in the presence of an alternative prey remains scarce. When having a food choice, predators may decrease parasite consumption, therefore, it is important to assess the role of parasites in the diet of predators in natural communities with different types of prey available. Our study aims to test whether common freshwater cyclopoids feed on trematode free-living stages (cercariae) when an alternative food source is present.
2. We experimentally studied ingestion rates of cyclopoids Macrocyclops distinctus fed with cercariae of trematode Diplostomum pseudospathaceum, a common and harmful parasite of freshwater fishes, and ciliates Paramecium caudatum (an alternative prey, known as suitable food for copepods). First, the feeding response of cyclopoids to different densities of each prey was studied. Then, feeding selectivity in the mixtures of cercariae and ciliates was tested.
3. Feeding rates of cyclopoids increased with prey densities (both ciliates and cercariae) but almost stopped growing at high prey densities, which indicated saturation (Holling type II functional response). In most cases, cyclopoids consumed cercariae at higher rates than ciliates. Maximum ingestion rates estimated from the obtained curves were 37 cercariae ind⁻¹ hr⁻¹ and 17 ciliate ind⁻¹ hr⁻¹.
4. When exposed to prey mixtures, cyclopoids fed on cercariae selectively. When cercariae were offered to cyclopoids at concentrations exceeding the saturation level, the ingestion of ciliates remained constantly low at all ciliate densities. In contrast, the ingestion of cercariae increased with rising cercariae densities even when ciliates were presented ad libitum, decreasing only at very high prey densities. Possible reasons of such feeding preferences are discussed.
5. Our study demonstrated that cyclopoids may prefer to feed on cercariae when there is an alternative food choice and can ingest cercariae at high rates. These experimental results could be extended to natural communities, suggesting that cyclopoids can reduce the transmission of parasites and contribute to the incorporation of parasite production in food webs of lentic ecosystems.

     

Factors affecting zooplankton feeding by the sea anemoneAiptasia pallida

Effects of various treatments on prey capture, prey ingestion and ingestion time of individualArtemia salina nauplii by the sea anemoneAiptasia pallida Verrill were studied in the laboratory. Exposure to crudeArtemia homogenate, 5 × 10^–4 M reduced glutathione or 5 × 10^–4 M proline significantly decreased the number ofArtemia that were captured and ingested but had no significant effect on the ingestion time of individualArtemia. Multiple captures increased the total ingestion time but decreased ingestion time per prey item. Results suggest that, under these conditions, the prey capture phase of zooplankton feeding was somewhat distinct from the ingestion phase since chemical stimuli that significantly reduced prey capture had no significant effect on ingestion time.     

The behaviour of an omnivorous protozoan affects the extent of induced morphological defence in a protozoan prey

1. The ciliate Euplotes octocarinatus responds to the presence of Stylonychia mytilus with a morphological transformation rendering its ingestion more difficult. Predation on Euplotes is reduced when an alternative prey, the flagellate Chlorogonium elongatum, is available. Lower predation is accompanied by reduced induction in Euplotes. 2. We quantified the motility of both ciliates in the presence and absence of Chlorogonium to test the hypothesis that the differential response in Euplotes is a consequence of behavioural changes affecting the encounter rate of the prey and the predator. 3. The results indicate that S. mytilus uses different feeding strategies for each prey. It is a filter feeder when small food particles (Chlorogonium) are abundant, however, it becomes a raptorial feeder when large prey with an escape capability (Euplotes) is available and small alternative prey are absent. 4. As the mobility of filter feeding Stylonychia is strongly limited, the presence of the flagellate may indirectly affect the defence level in Euplotes by reducing the frequency of contacts with the predator. 5. An experiment with Chaetogaster diastrophus, a more specialised predator not affected by the presence of Chlorogonium, as well as direct manipulation of the encounter rate by changing the surface area available for the crawling ciliates, supported the encounter rate hypothesis.     

Prey features affecting ingestion rates by Acanthocyclops robustus (Copepoda: Cyclopoida) on zooplankton

Summary (1) Ingestion rates by adult female and juvenile Acanthocyclops robustus on a number of prey types were measured at a prey concentration of 100/l in experimental volumes of 300–400 ml. (2) For the adult predator, Synchaeta pectinata was most vulnerable (22.3, standard error 1.4, prey ingested per predator per day) as compared to Brachiomus calyciflorus, Brachionus diversicornis, Keratella cochlearis (two morphs), Asplanchna priodonta, Polyarthra major, Synchaeta kitina, Pompholyx sulcata, Daphnia spec., and Bosmina longirostris. For these latter prey, the lowest ingestion rate was on one morph of K. cochlearis and the highest on A. priodonta, being, respectively, 1.0, SE 0.5, and 11.3, SE 1.0, prey per predator per day. (3) With regard to the juvenile predator (mostly copepodite stages I, II and III), ingestion rates on K. cochlearis and P. sulcata were low (respectively 1.2, SE 0.7, and 0.3, SE 0.1, prey per predator per day) but quite high on S. kitina (5.7, SE 0.6). (4) In addition, the effect of increasing prey concentration on the ingestion rate (functional response) by the adult female predator was examined for B. calyciflorus, K. cochlearis, S. pectinata, S. kitina and Daphnia spec.. Increases in ingestion rate with prey density were minimal for B. calyciflorus and K. cochlearis, greater for Daphnia spec., still greater for S. pectinata and of greatest magnitude for S. kitina. (5) The reasons for these results are discussed with particular reference to prey features.     

Differential feeding by common heterotrophic protists on four Scrippsiella species of similar size

The dinoflagellate genus Scrippsiella is known to cause red tides. Mortality due to predation should be assessed in order to understand the population dynamics of Scrippsiella species. However, predation has been explored only in a few species. In this study, we examined feeding by common heterotrophic dinoflagellates Oxyrrhis marina, Gyrodinium dominans, Polykrikos kofoidii, Oblea rotunda, and Pfiesteria piscicida, and a ciliate Strombidinopsis sp., on four Scrippsiella species, of similar size, namely Scrippsiella acuminata, Scrippsiella donghaiensis, Scrippsiella lachrymosa, and Scrippsiella masanensis. All the heterotrophic protists tested could feed on all the four Scrippsiella species. However, the numerical and functional responses of P. kofoidii to the mean prey concentration were apparently different between the Scrippsiella species. With increasing prey concentration, the growth and ingestion rates of P. kofoidii on S. lachrymosa increased rapidly, and then saturated similar to those on S. acuminata, as previously reported, but those on S. donghaiensis continuously decreased. The cells of S. donghaiensis lysed P. kofoidii cells. In contrast, the growth and ingestion rates of P. kofoidii on S. masanensis were not significantly related to the prey concentration. At similarly high mean prey concentration, the growth and ingestion rates of G. dominans were significantly different between the four Scrippsiella species Therefore, differences in the growth and/or ingestion rates of G. dominans and P. kofoidii on the four Scrippsiella species might result in different ecological niches of both the predator and prey species.     

Dynamics and Nutritional Ecology of a Nanoflagellate Preying Upon Bacteria

Ingestion and growth rates of the nanoflagellate predator Ochromonas danica feeding on the bacterium Pseudomonas fluorescens were quantified in laboratory cultures. Bacterial prey were grown under four nutritional conditions with respect to macronutrient elements: C-limited, N-limited, P-limited, and balanced. Ingestion and growth rates were saturating functions of prey abundance when preying upon nutritionally balanced, C-limited, and P-limited bacteria but were unimodal functions of abundance when preying on N-limited bacteria. At saturating prey concentrations, the ingestion rate of C-limited prey was about twice that of prey in other nutritional states, while at subsaturating prey concentrations, the ingestion rates of both C- and N-limited prey were higher than those of prey in other nutritional states. Over all prey concentrations, growth was most rapid on balanced and C-limited prey and generally lowest for P-limited prey. Due to the unimodal response of growth rate to abundance of N-limited prey, growth rate on N-limited prey approached that obtained on balanced and C-limited prey when prey were available at intermediate abundances. The accumulation of recycled N increased with the growth rate of O. danica. Recycling of N was highest when O. danica was feeding upon P-limited prey. The accumulation of recycled P increased with growth rate for balanced and N-limited prey, but not for P-limited prey, which consistently had low accumulation of recycled P. The low growth rate and negligible recycling of P for O. danica preying on P-limited prey is consistent with the theory of ecological stoichiometry and resembles results found for crustacean zooplankton, especially in the genus Daphnia. Potentially, the major predators of bacterioplankton and a major predator of phytoplankton play analogous roles in the trophic dynamics and biogeochemistry of aquatic ecosystems.     

Prey-handling Behaviour of Newly Hatched Snakes in Two Species of the Genus Elaphe with Comparison to Adult Behaviour

The prey-handling behaviour of two species of Asian ratsnakes was studied in the laboratory. In experiment 1, effects of prey size and type (mouse, lizard and frog) on capture position, direction of ingestion, condition of prey at ingestion, and prey-handling method were investigated using newly hatched Elaphe quadrivirgata. Prey size did not affect these variables except prey-handling method in frog trials: large frogs were more frequently constricted after a delay of more than 1 s than small frogs, and small frogs were usually simply seized. On the other hand, prey type affected prey-handling method: mice and lizards were more frequently constricted or pinioned than frogs. When hatchlings of E. quadrivirgata tried to coil around a prey animal immediately after striking, they frequently failed or released their coils within 10 s after striking. In experiment 2, prey-handling behaviour of adult E. climacophora was examined with mice of various sizes. Adult E. climacophora tended to constrict large mice immediately after striking, whereas they simply seized small mice. Only one out of 38 mice which were constricted immediately after striking was released from the coils within the subsequent 10 s. Large mice were killed prior to ingestion, whereas small mice were swallowed alive. Large mice tended to be swallowed head first. Experiment 3 was conducted to investigate effects of mouse size on prey-handling behaviour of newly hatched E. climacophora. Mouse size affected condition of prey at ingestion and prey-handling method but not capture position and direction of ingestion. Possible relationships between feeding ecology and the differences of prey-handling behaviour among Elaphe are discussed.     

PHAGOTROPHY IN GYMNODINIUM FUNGIFORME (PYRRHOPHYTA): THE PEDUNCLE AS AN ORGANELLE OF INGESTION1

The non-photosynthetic phagotrophic dinoflagellate, Gymnodinium fungiforme Anissimova, ingests prey cytoplasm through a highly extensible structure called the peduncle. Although the peduncle is not observable when G. fungiforme is swimming, it protrudes 8–12 μm from the sulcal-angular vicinity of the cell during feeding, and is approximately 3.3 μm wide when the cytoplasm of its prey is flowing through it. A circular-oval ring of overlapping microtubules, the ‘microtubular basket’ may be seen in transmission electron microscope sections of G. fungiforme and it is inferred that this structure is a cross section of a retracted peduncle. The microtubular basket-peduncle complex is discussed in relation to similar structures in other dinoflagellates and to the tentacle of the suctorian ciliates which have a homologous ingestion system.     

Feeding responses of Asplanchna brightwelli (rotifera): laboratory and field studies

Laboratory-reared A. brightwelli were offered 16 different prey rotifer species from the genera Anuraeopsis, Brachionus, Epiphanes, Filinia, Hexarthra, Lecane, Lepadella, Pompholyx, Proalides and Trichocerca. Feeding responses (prey encounter, escape, capture, rejection and ingestion) were recorded. In general, the predator's ingestion time was positively correlated with prey length. B. falcatus and H. intermedia were never captured. Once captured, smaller rotifer species were ingested. Gut contents of field-collected A. brightwelli revealed increased occurrence of prey numbers when concentrated plankton samples were preserved after some delay.     

Optimal diet theory: behavior of a starved predatory snail

Summary The tenets of optimal foraging theory are used to contrast the behavior of the predatory snail Acantina spirata when feeding on the barnacles Balanus glandula and Chthamalus fissus under conditions of satiation and starvation. As predicted in optimal diet models, A. spirata is less selective (ratio of attack frequency on a prey species to number of individuals available) when the higher ranking prey has low abundance. When given a choice, starved snails attack both barnacle species equally, whereas satiated individuals preferentially attack B. glandula, the more profitable prey (ash-free dry weight of barnacles ingested per unit handling time). Under starvation conditions, equal attack frequency does not result in equal prey species consumption because Acanthina spirata is more successful at attacking C. fissus than B. glandula.The assumption of constant prey encounter rates in optimal diet models is not met when A. spirata goes from a state of satiation to starvation. The encounter rate on B. glandula is lowered due to a decrease in attack success. A loss of feeding skills in starved A. spirata is responsible for the greater difficulty snails have in gaining access through the opercular plates of B. glandula.Behavioral changes in A. spirata as snails pass from satiation to hunger translate into an energetic disadvantage during feeding for hungry snails for two reasons. First, higher prey handling times result in a decreased rate of biomass intake. Second, alteration in the relative attack frequency between barnacle species, combined with a decrease in attack success on the more profitable prey leads to more frequent ingestion of the less profitable prey.     

Differences in predation among morphotypes of the rotifer Asplanchna silvestrii

1. Interactions were observed between three morphotypes of the predatory rotifer Asplanchna silvestrii and six different prey (Brachionus plicatilis, B. rotundiformis, B. pterodinoides, B. satanicus, Hexarthra jenkinae and copepod nauplii) to understand the differences in feeding abilities among morphotypes that may have led to the evolution of this predator polymorphism. The outcome of predation events was affected significantly, both by predator morphotype and prey type. Predator morphotypes also interacted differently with different prey types. 2. The two smaller morphotypes, the saccate and the cruciform, responded similarly to prey overall, except that the smallest morphotype (saccate) was unable to ingest the most mobile prey (nauplii) and less able to ingest relatively large prey (B. plicatilis). The largest morphotype, the campanulate, had the highest encounter rate with prey, but the lowest probability of attack after encounter, so that it consumed far fewer prey per feeding bout than did the smaller morphotypes. This may have been because campanulates prefer larger prey than used in this study. 3. Highly mobile prey (H. jenkinae and copepod nauplii) were much less susceptible to predation than the less mobile Brachionus species. While evasiveness reduced attacks by saccates and cruciforms, campanulates did not have a significantly lower attack rate on H. jenkinae and copepod nauplii than on less evasive prey. Large body size moderately defended B. plicatilis against ingestion by saccates only. The short-spined B. satanicus was the only prey that was rejected after capture, resulting in lower ingestion probabilities for B. satanicus than other brachionid prey.     

Morphological and functional bases of durophagy in the queen triggerfish,Balistes vetula (Pisces,tetraodontiformes)

Tetraodontiform fishes are characterized by jaws specialized for powerful biting and a diet dominated by hard-shelled prey. Strong biting by the oral jaws is an unusual feature among teleosts. We present a functional morphological analysis of the feeding mechanism of a representative tetraodontiform, Balistes vetula. As is typical for the order, long, sharp, strong teeth are mounted on the short, robust jaw bones of B. vetula. The neurocranium and suspensorium are enlarged and strengthened to serve as sites of attachment for the greatly hypertrophied adductor mandibulae muscles. Electromyographic recordings made from 11 cranial muscles during feeding revealed four distinct behaviors in the feeding repertoire of B. vetula. Suction is used effectively to capture soft prey and is associated with a motor pattern similar to that reported for many other teleosts. However, when feeding on hard prey, B. vetula directly bit the prey, exhibiting a motor pattern very different from that of suction feeding. During buccal manipulation, repeated cycles of jaw opening and closing (biting) were coupled with rapid movement of the prey in and out of the mouth. Muscle activity during buccal manipulation was similar to that seen during bite-captures. A blowing behavior was periodically employed during prey handling, as prey were forcefully “spit out” from the mouth, either to reposition them or to separate unwanted material from flesh. The motor pattern used during blowing was distinct from similar behaviors described for other fishes, indicating that this behaviors may be unique to tetraodontiforms. Thus B. vetula combines primitive behaviors and motor patterns (suction feeding and buccal manipulation) with specialized morphology (strong teeth, robust jaws, and hypertrophied adductor muscles) and a novel behavior (blowing) to exploit armored prey such as sea urchins molluscs, and crabs. © 1993 Wiley-Liss, Inc.     

The effects of group size on per capita ingestion in flatworms

1. We evaluated the effect of group size on the per capita ingestion rates of three species of flatworm, two of which actively group with conspecifics (Dugesia tigrina, D, dorotocephala) and employ mucus to capture prey, and a third species (Mesostoma ehrenbergii) that does not actively group but does use mucus to capture prey. 2. As flatworm group size increased, daily per capita ingestion first increased and then decreased for D. tigrina and D. dorotocephala. In the case of D. tigrina this pattern was observed even at low predator densities. Ingestion rates of M. ehrenbergii were largely unaffected by group size. 3. Results suggest that the observed changes in per capita ingestion rates with changes in group size previously reported for D. tigrina are related to their tendency for active grouping and are not directly a consequence of prey capture technique or experimental design. 4. We argue that freshwater triclads in general, and D. tigrina in particular, represent an ideal model system for the development and testing of group foraging theory.     

Killing them softly: Ontogeny of jaw mechanics and stiffness in mollusk-feeding freshwater stingrays

Durophagous predators consume hard-shelled prey such as bivalves, gastropods, and large crustaceans, typically by crushing the mineralized exoskeleton. This is costly from the point of view of the bite forces involved, handling times, and the stresses inflicted on the predator's skeleton. It is not uncommon for durophagous taxa to display an ontogenetic shift from softer to harder prey items, implying that it is relatively difficult for smaller animals to consume shelled prey. Batoid fishes (rays, skates, sawfishes, and guitarfishes) have independently evolved durophagy multiple times, despite the challenges associated with crushing prey harder than their own cartilaginous skeleton. Potamotrygon leopoldi is a durophagous freshwater ray endemic to the Xingu River in Brazil, with a jaw morphology superficially similar to its distant durophagous marine relatives, eagle rays (e.g., Aetomylaeus, Aetobatus). We used second moment of area as a proxy for the ability to resist bending and analyzed the arrangement of the mineralized skeleton of the jaw of P. leopoldi over ontogeny using data from computed tomography (CT) scans. The jaws of P. leopoldi do not resist bending nearly as well as other durophagous elasmobranchs, and the jaws are stiffest nearest the joints rather than beneath the dentition. While second moment has similar material distribution over ontogeny, mineralization of the jaws under the teeth increases with age. Neonate rays have low jaw stiffness and poor mineralization, suggesting that P. leopoldi may not feed on hard-shelled prey early in life. These differences in the shape, stiffness and mineralization of the jaws of P. leopoldi compared to its durophagous relatives show there are several solutions to the problem of crushing shelled prey with a compliant skeleton.     

Identification of trophic interactions between <Emphasis Type="Italic">Macrolophus caliginosus</Emphasis> (Heteroptera: Miridae) and <Emphasis Type="Italic">Myzus persicae</Emphasis> (Homoptera: Aphididae) using real time PCR

Understanding food web interactions in native or agricultural ecosystems is an important step towards establishing sustainable pest management strategies. While the role of generalist predators as biological control agents is increasingly appreciated, the study of trophic interactions between individual predator species and their prey provides practical difficulties. Recently, different approaches have been suggested to determine prey items from predator guts using molecular methods. Macrolophus caliginosus is a generalist predator active in herbaceous agro-ecosystems. We developed a system to identify the DNA of its prey after ingestion, using Myzus persicae as a model. Esterase (MpEST) and cytochrome oxidase I (MpCOI) genes were targeted in the aphid, while M. caliginosus COI gene was used as control for predator DNA. Real time PCR proved to be specific and sensitive enough to detect prey DNA upon ingestion after feeding experiments. The system provided a linear amplification response with only 10 fg of prey genomic DNA as template. The detection system of MpCOI gene was more sensitive than MpEST, while the detection period was similar for both genes. Possibilities for using the system in ecological and biosafety studies with regard to sustainable pest management are discussed.

A Dinoflagellate Amylax triacantha with Plastids of the Cryptophyte Origin: Phylogeny,Feeding Mechanism,and Growth and Grazing Responses

The gonyaulacalean dinoflagellates Amylax spp. were recently found to contain plastids of the cryptophyte origin, more specifically of Teleaulax amphioxeia. However, not only how the dinoflagellates get the plastids of the cryptophyte origin is unknown but also their ecophysiology, including growth and feeding responses as functions of both light and prey concentration, remain unknown. Here, we report the establishment of Amylax triacantha in culture, its feeding mechanism, and its growth rate using the ciliate prey Mesodinium rubrum (= Myrionecta rubra) in light and dark, and growth and grazing responses to prey concentration and light intensity. The strain established in culture in this study was assigned to A. triacantha, based on morphological characteristics (particularly, a prominent apical horn and three antapical spines) and nuclear SSU and LSU rDNA sequences. Amylax triacantha grew well in laboratory culture when supplied with the marine mixotrophic ciliate M. rubrum as prey, reaching densities of over 7.5 × 10³ cells/ml. Amylax triacantha captured its prey using a tow filament, and then ingested the whole prey by direct engulfment through the sulcus. The dinoflagellate was able to grow heterotrophically in the dark, but the growth rate was approximately two times lower than in the light. Although mixotrophic growth rates of A. triacantha increased sharply with mean prey concentrations, with maximum growth rate being 0.68/d, phototrophic growth (i.e. growth in the absence of prey) was ?0.08/d. The maximum ingestion rate was 2.54 ng C/Amylax/d (5.9 cells/Amylax/d). Growth rate also increased with increasing light intensity, but the effect was evident only when prey was supplied. Increased growth with increasing light intensity was accompanied by a corresponding increase in ingestion. In mixed cultures of two predators, A. triacantha and Dinophysis acuminata, with M. rubrum as prey, A. triacantha outgrew D. acuminata due to its approximately three times higher growth rate, suggesting that it can outcompete D. acuminata. Our results would help better understand the ecophysiology of dinoflagellates retaining foreign plastids.     

Prey handling time and ingestion probability for Mesocyclops sp. predation on small cladoceran species Bosmina longirostris, Bosminopsis deitersi, and Scapholeberis mucronata

We compared the vulnerability of small cladoceran species (Bosminopsis deitersi, Bosmina longirostris, and Scapholeberis mucronata) to predation by Mesocyclops sp. in the laboratory based on prey handling time and ingestion probability. We also estimated the effects of ontogenetic changes on handling time by testing prey of various body sizes. All tested prey species showed an increasing pattern of handling time along with growth (increase of body size). For juveniles smaller than 0.3mm, the prey handling time was similar for B. deitersi and B. longirostris, but markedly longer for S. mucronata. Mesocyclops sp. rejected large (>0.35mm) B. longirostris and S. mucronata soon after capture and consequently showed a low probability of successful ingestion, whereas most large individuals of B. deitersi were consumed. The shorter handling time and higher ingestion probability of small juveniles indicate that the copepods ingest small juveniles more efficiently than larger individuals. Thus, it seems that the vulnerability of small cladocerans to copepod predation differs ontogenetically, with the greatest vulnerability being during the juvenile period. The ontogenetic reduction in the vulnerability of B. longirostris and S. mucronata was shown in the rapidly reduced ingestion probability as well as by the increase in prey handling time for large individuals. The results show that the vulnerability to predation by copepods of B. longirostris and S. mucronata reduces more quickly with increasing size than does that of B. deitersi, and it seems that the former two species are more resistant to copepod predation.     

Feeding by Phototrophic Red-Tide Dinoflagellates on the Ubiquitous Marine Diatom Skeletonema costatum

ABSTRACT We investigated feeding by phototrophic red‐tide dinoflagellates on the ubiquitous diatom Skeletonema costatum to explore whether dinoflagellates are able to feed on S. costatum, inside the protoplasm of target dinoflagellate cells observed under compound microscope, confocal microscope, epifluorescence microscope, and transmission electron microscope (TEM) after adding living and fluorescently labeled S. costatum (FLSc). To explore effects of dinoflagellate predator size on ingestion rates of S. costatum, we measured ingestion rates of seven dinoflagellates at a single prey concentration. In addition, we measured ingestion rates of the common phototrophic dinoflagellates Prorocentrum micans and Gonyaulax polygramma on S. costatum as a function of prey concentration. We calculated grazing coefficients by combining field data on abundances of P. micans and G. polygramma on co‐occurring S. costatum with laboratory data on ingestion rates obtained in the present study. All phototrophic dinoflagellate predators tested (i.e. Akashiwo sanguinea, Amphidinium carterae, Alexandrium catenella, Alexandrium tamarense, Cochlodinium polykrikoides, G. polygramma, Gymnodinium catenatum, Gymnodinium impudicum, Heterocapsa rotundata, Heterocapsa triquetra, Lingulodinium polyedrum, Prorocentrum donghaiense, P. micans, Prorocentrum minimum, Prorocentrum triestinum, and Scrippsiella trochoidea) were able to ingest S. costatum. When mean prey concentrations were 170–260 ng C/ml (i.e. 6,500–10,000 cells/ml), the ingestion rates of G. polygramma, H. rotundata, H. triquetra, L. polyedrum, P. donghaiense, P. micans, and P. triestinum on S. costatum (0.007–0.081 ng C/dinoflagellate/d [0.2–3.0 cells/dinoflagellate/d]) were positively correlated with predator size. With increasing mean prey concentration of ca 1–3,440 ng C/ml (40–132,200 cells/ml), the ingestion rates of P. micans and G. polygramma on S. costatum continuously increased. At the given prey concentrations, the maximum ingestion rates of P. micans and G. polygramma on S. costatum (0.344–0.345 ng C/grazer/d; 13 cells/grazer/d) were almost the same. The maximum clearance rates of P. micans and G. polygramma on S. costatum were 0.165 and 0.020 μl/grazer/h, respectively. The calculated grazing coefficients of P. micans and G. polygramma on co‐occurring S. costatum were up to 0.100 and 0.222 h, respectively (i.e. up to 10% and 20% of S. costatum populations were removed by P. micans and G. polygramma populations in 1 h, respectively). Our results suggest that P. micans and G. polygramma sometimes have a considerable grazing impact on populations of S. costatum.     

Predation by Neomysis mercedis: effects of temperature, Daphnia magna size and prey density on ingestion rate and size selectivity

1. Neomysis mercedis predation rates on Daphnia magna were determined under laboratory conditions. There were generally no consistent differences between the number of Daphnia ingested at 10 and 14°C. 2. At each temperature, the number of prey consumed increased with mysid size and decreased with Daphnia size. 3. For small prey the relationship between ingestion rate and prey density represented a Type II functional response. However, for larger prey there was no significant relationship between density of prey and consumption by mysids. 4. The pattern of size-selective predation by Neomysis was studied to test the optimal foraging hypothesis. For prey populations with mixed size classes, the smallest size of prey was consumed most frequently but intermediate size prey provided the greatest biomass. These observations are contrary to our predictions based on calculations of profitability of different sizes of prey.