Foraging behaviour and prey size of the painted stork

The foraging behaviour of painted stork Mycteria leucocephala was studied during 2004–2006 at 14 different sites in the Delhi region, India. Observations were recorded on 131 individuals, including 29 juvenile birds using a video camera. Recordings were also made at the nesting colony in Delhi zoo to study the prey sizes regurgitated to nestlings. The results confirm that the painted stork is a tactile forager and exclusively piscivorous. Foraging group size ranged from 1 to 18 individuals. Per 5 min foot stirring rates in the vegetated habitats were significantly higher than in non-vegetated habitats. The attempt rate and feeding rate in the breeding season were significantly higher than that in the non-breeding season. Prey sizes taken in the breeding season were significantly smaller than those taken in the non-breeding season. About 80% fish fed to the chicks were smaller than 10 cm. Young chicks were offered smaller prey compared with older chicks. The variations in foraging parameters are discussed in relation to habitats and their conservation in the Delhi region.     

Effects of water level changes and wading bird abundance on the foraging behaviour of blacknecked storks Ephippiorhynchus asiaticus in Dudwa National Park, India

The effect of water level changes and wading birds' abundance on the foraging behaviour of the blacknecked stork (BNS)Ephippiorhynchus asiaticus was studied from January 1995 to June 1997 in Dudwa National Park, Uttar Pradesh. Our observations indicate that BNS territoriality increased as food levels became depleted, resulting in increased rates of aggression towards intruders. Chasing or aggression was more intense during the early period (February and March) than the late period (April, May and June). Most of (> 50%) the aggressive encounters were observed between 0600 and 1000 h of the day. Seventeen species (including BNS) were observed interacting with BNS, throughout the study period. Most interactions were with the spoonbill,Platalea leucorodia (67.4%), followed by the whitenecked stork,Ciconia episcopus (16.6%). The distance (while foraging) between BNS and other wading birds varied significantly (P < 0001) between years indicating that BNS and other water birds foraged at different water depths and thereby explored the wetlands fully. Spoonbills were chased often; the number varied from 1 to 43 birds. BNS occasionally accepted the presence of other wading birds, including spoonbills and started foraging amidst them. This led to successful foraging of BNS (solitary feeder). Other fish-eating bird species and their numbers also limited the food consumption of foraging BNS as they had to spend time chasing away the intruders. Availability of the preferred prey fish species,Heteropnestus fossilis, forced BNS to stay throughout the year in their respective territories. High (> 60 cm) water levels were not suitable for BNS even though the patch had high prey abundance.     

The effects of perceived competition and parasitism on the foraging behaviour of the upland bully (Eleotridae)

Prey choice by fish is subject to many constraints, some of which may interact to determine the relative preference of fish for prey with different profitabilities. The constraining effects of parasitism and perceived competition on foraging behaviour were examined in the upland bully, Gobiomorphus breviceps . In the laboratory, bullies faced with a choice of prey items of two different sizes chose the larger prey significantly more often than the smaller ones. The presence of a conspecific fish near the source of large prey significantly reduced the bullies'preference for larger prey. Neither the size of the test fish, nor the number of digenean metacercarial cysts they harboured, had any influence on their relative preference for larger prey, or on how that preference was dampened by the presence of a competitor. The threat of competition appears to be a more important constraint on prey choice in upland bullies than parasitism.     

Sibling cannibalism among juvenile vundu under controlled conditions. I. Cannibalistic behaviour, prey selection and prey size selectivity

Sibling cannibalism among vundu Heterobranchus longifilis larvae started at the age of 4 days, with the prey caught tail-first then swallowed up to the head, which was eventually discarded (type I cannibalism). At 17 days old, this type of cannibalism vanished and was replaced by the ingestion of the whole prey (type II cannibalism), which could only be exerted by predators six times as heavy as their prey. Type II cannibalism consisted of a seemingly opportunistic ambush attack by a formerly passive predator towards a disorientated prey. It required no preliminary aggression or chase, or even contact with the prey, suggesting that the attack was not mediated by the tactile sense, and that cannibalism was independent of aggressive behaviour. When alternative food resources (formulated feed, live tilapia prey) were available, the intensity of cannibalism decreased but pellet-eaters or tilapia predators always achieved lower growth rates than those feeding on conspecifics, suggesting that cannibalism was the most advantageous foraging tactic. Losses to cannibalism among populations of 30-day old juvenile vundu with an initial ratio of 4% of cannibals were as high as 75·5–79·9% over 15 days. Predation peaked during the first days (up to 2·8 prey C⁻¹ day⁻¹), then vanished progressively as surviving prey grew faster than cannibals and escaped their predation. Cannibals preferred consuming the largest prey available with respect to the logistics of cannibalism (body weight ratio of 6·0). This preference for large prey was interpreted both as a foraging tactic aiming to maximize the energetic return, and as foraging strategy enabling the cannibals to exploit their prey as long as possible. Based on these data, comprehensive models of the impact of cannibalism on vundu populations were developed.     

Foraging habitat determines predator–prey size relationships in marine fishes

Predator–prey size (PPS) relationships are determined by predator behaviour, with the likelihood of prey being eaten dependent on their size relative to that of the consumer. Published PPS relationships for 30 pelagic or benthic marine fish species were analysed using quantile regression to determine how median, lower and upper prey sizes varied with predator size and habitat. Habitat effects on predator foraging activity/mode, morphology, growth and natural mortality are quantified and the effects on PPS relationships explored. Pelagic species are more active, more likely to move by caudal fin propulsion and grow more rapidly but have higher mortality rates than benthic species, where the need for greater manoeuvrability when foraging in more physically complex habitats favours ambush predators using pectoral fin propulsion. Prey size increased with predator size in most species, but pelagic species ate relatively smaller prey than benthic predators. As pelagic predators grew, lower prey size limits changed little, and prey size range increased but median relative prey size declined, whereas the lower limit increased and median relative prey size was constant or increased in benthic species.     

Linking piscivory to spatial–temporal distributions of pelagic prey fishes with a visual foraging model

A visual foraging model (VFM) used light-dependent reaction distance and capture success functions to link observed prey fish abundance and distribution to predation rates and the foraging performance of piscivorous cutthroat trout Oncorhynchus clarki in Lake Washington (WA, U.S.A.). Total prey density did not correlate with predation potential estimated by the foraging model for cutthroat trout because prey were rarely distributed in optically favourable conditions for detection. Predictions of the depth-specific distribution and timing of cutthroat trout foraging were qualitatively similar to diel stomach fullness patterns observed in field samples. Nocturnal foraging accounted for 34–64% of all prey fish consumption in simulations for 2002 and 2003. Urban light contamination increased the access of nocturnally foraging cutthroat trout to vertically migrating prey fishes. These results suggest that VFMs are useful tools for converting observed prey fish density into predictions of predator consumptions and behavioural responses of predators to environmental change.     

The influence of prey size,sediment thickness and fish size on consumption in common sole (Solea solea L.)

This study determined prey consumption in common sole as a function of prey size (0–0.5, 1–1.5, 2–2.5 and 4–5 g), sediment thickness (20 cm and 2 cm) and fish size (50 g, 125 g or 300 g). Prey consumption (in numbers of prey eaten per fish per day) was reduced with increasing prey size and sediment thickness, and was increased with increasing fish size (p < .001 for all factors). All 3 factors showed significant two way interactions (p < .001) when expressed in numbers of prey eaten. Prey consumption decreased with prey size when prey could not escape by burying (2 cm of sediment thickness) irrespective of fish size. We suggest that increasing effort to ingest and handle larger prey played a role. Prey consumption increased with fish size when prey could not bury (2 cm of sediment thickness). However, when prey was able to bury (at 20 cm sediment thickness) prey consumption was similar irrespective of fish size (p < .001 for interaction fish size × sediment). This interaction suggests that with increasing fish size there is an increasing mismatch between foraging adaptation and prey burial depth. This may explain the dominance of crustaceans in the diet of adult common sole in nature, despite the high abundance of polychaetes.     

FORAGING OF JUVENILE MONK SEALS AT FRENCH FRIGATE SHOALS, HAWAII

Emaciation and poor survivorship of juvenile Hawaiian monk seals at French Frigate Shoals atoll prompted a study of their foraging, using video camera technology ( crittercam ). Nine juveniles between the ages of 1 and 3 yr (six males, three females) were fitted with crittercam to identify their foraging habitat and feeding behavior. All feeding was directed at small (≤ 10 cm), cryptic, benthic prey. Older seals (ages 2 and 3), varied in their foraging intensity with most of their attention directed at shallow atoll depths (10–30 m). In contrast, the three yearlings focused all their feeding in the sand fields (50–100 m) on the atoll's outer slope. Bottom trawls were used to assess the prey abundance of the sand habitat and found 70% of the numerical catch was flounder ( Bothidae ). Extrapolating the yearlings' prey capture rate (0.13/min, derived from the crittercam video) over their total bottom time yielded an estimated 1–1.3 kg/day of flounder. The mean size of flounder (5 ± 1.7 cm) caught in the bottom trawls was close to the size at which larval flounder settle from the plankton (3 cm), suggesting that localized changes in oceanography could directly impact the seals' prey supply. Extensive use of sand communities by young seals may be the strongest link yet identified between juvenile survivorship and oceanographic dynamics.     

Foraging behavior and energetics of Great Egrets and Snowy Egrets at interior rivers and weirs

ABSTRACT.   Wading birds may use different foraging methods and prey capture techniques in particular habitats or under specific conditions. We measured foraging behavior and its energetic costs for Great Egrets ( Ardea alba ) and Snowy Egrets ( Egretta thula ) at two weirs (small overflow dams that raise water levels in a stream or river) and in two naturally flowing rivers in Kansas in May and June 2000 and 2005. We observed 99 randomly selected birds (38 Great Egrets and 61 Snowy Egrets) for 1513 min, and noted strike rate, prey capture rate, capture efficiency, prey size, and social interactions. In addition, 30 of these birds were observed for 504 min to estimate ambulation velocities and foraging energetics. Both species had higher strike rates and prey capture rates in rivers, but caught larger fish at weirs. Capture efficiency was higher for Snowy Egrets at weirs, but did not differ between microhabitats for Great Egrets. Snowy Egrets had higher rates of conspecific aggression at weirs than in rivers, but little aggression was documented for Great Egrets. Established algorithms suggest that, while foraging in rivers, Snowy Egrets had similar costs for changes in velocity. Changes in ambulation velocity for Great Egrets were greater at weirs than rivers. For both species, the percentage of time spent standing was twice as high at weirs as in rivers. Both species also used low-cost foraging strategies at weirs that yielded larger fish, so net energetic gains at weirs were higher than in rivers. Weirs appear to be more important to Snowy Egrets than to Great Egrets. Estimates of energy gains and expenses provide valuable predictive power for understanding egret behavior.     

Ontogenetic changes in foraging tactics of the piscivorous cornetfish <Emphasis Type="Italic">Fistularia commersonii</Emphasis>

Foraging behaviors of the piscivorous cornetfish Fistularia commersonii were observed at shallow reefs in Kuchierabu-jima Island, southern Japan. This fish foraged on two types of prey fishes: one was reef fish that typically dwell on or near substrata (e.g., Tripterygiidae and Labridae), and the other was pelagic fish that shoal in the water column (e.g., Clupeidae and Carangidae). The prey sizes, prey types and foraging behaviors changed as the predator size increased. Prey sizes were largely limited by gape size of the cornetfish, and small predators consumed small prey. The small cornetfish (10–30 cm in total length) fed only on reef fish captured after stalking (where the fish slowly approaches the prey and then suddenly attacks). The stalking was done either solitarily or in foraging association with conspecifics. Large fish (30–120 cm) fed on both types of fishes by stalking and/or chasing (where the fish chases the prey using its high mobility and attacks), either solitarily or in foraging association with con- or heterospecifics. Thus, chasing was only performed by the large cornetfish against pelagic prey fish in associative foraging with other con- and heterospecific predators. As their body sizes increased, F. commersonii began to show a diversification of foraging behaviors, which was strongly related not only to the habitat types and anti-predatory behaviors of the prey fishes but also to associative foraging with con- or heterospecifics, which improves their foraging success.     

Effects of crayfish size,orientation, and movement on the reactive distance of largemouth bass foraging in clear and turbid water

Laboratory experiments were performed in clear and turbid water to determine the effects of prey size, orientation, and movement on the reactive distance of largemouth bass (Micropterus salmoides) when feeding on crayfish (Procambarus acutus). In clear water, the reactive distance increased linearly with an increase in prey size, and prey movement resulted in a significant increase in the reactive distance. Prey orientation (head-on versus perpendicular) did not change the reactive distances. In moderately turbid water, the reactive distance did not increase with increased prey size, and prey movement did not result in any changes in the reactive distance. The absence of any effects of prey orientation in clear water or prey movement in turbid water is inconsistent with results from studies using different species (primarily planktivorous fish). I propose that largemouth bass change their foraging tactics as prey visibility changes. When prey are highly visible (low turbidity), predators attack (react) only after prey recognition, which is based on multiple cues such as prey size (length, width) and movement. When prey are less visible (high turbidity), predators attack immediately upon initial prey sighting, which does not depend on prey size or movement.     

The effects of predator size, temperature, and prey characteristics on gastric evacuation in whiting

No effect of prey size on gastric evacuation rate was found in whiting Merlangius merlangus .Prey energy density explained most of the data variation among fish prey, and evacuation time increased by a factor 1·6–1·7 with prey energy density increasing from 3·4 to 5·6 kJ g⁻¹. The power model expanded to include predator size, temperature, and prey energy density could describe gastric evacuation in whiting fed fish prey. Krill Meganyctiphanes norvegica was evacuated at a rate similar to fish prey of equal energy density, while the evacuation of brown shrimp Crangon crangon took almost twice as long.     

Prey capture and selection throughout the breeding season in a deep‐diving generalist seabird,the thick‐billed murre

Generalist seabirds forage on a variety of prey items providing the opportunity to monitor diverse aquatic fauna simultaneously. For example, the coupling of prey consumption rates and movement patterns of generalist seabirds might be used to create three‐dimensional prey distribution maps (‘preyscapes’) for multiple prey species in the same region. However, the complex interaction between generalist seabird foraging behaviour and the various prey types clouds the interpretation of such preyscapes, and the mechanisms underlying prey selection need to be understood before such an application can be realized. Central place foraging theory provides a theoretical model for understanding such selectivity by predicting that larger prey items should be 1) selected farther from the colony and 2) for chick‐feeding compared with self‐feeding, but these predictions remain untested on most seabird species. Furthermore, rarely do we know how foraging features such as handling time, capture methods or choice of foraging location varies among prey types. We used three types of animal‐borne biologgers (camera loggers, GPS and depth‐loggers) to examine how a generalist Arctic seabird, the thick‐billed murre Uria lomvia, selects and captures their prey throughout the breeding season. Murres captured small prey at all phases of a dive, including while descending and ascending, but captured large fish mostly while ascending, with considerably longer handling times. Birds captured larger prey and dove deeper during chick‐rearing. As central place foraging theory predicted, birds travelling further also brought bigger prey items for their chick. The location of a dive (distance from colony and distance to shore) best explained which prey type was the most likely to get caught in a dive, and we created a preyscape surrounding our study colony. We discuss how these findings might aid the use of generalist seabirds as bioindicators.     

Underwater predatory behaviour of the American mink (Mustela vison)

Fishing behaviour of the American mink ( Mustela vison Schreber) was investigated in the laboratory. Data were recorded using ciné film and tape recorded commentaries. Three species of prey were presented to mink, namely, carp ( Cyprinus curpio ), goldfish ( Carassius auratus ) and minnows ( Phoxinus phoxinus ).
It was found to be necessary to train ranch-bred mink to enter water and catch fish; young mink appeared to be easier to train than adults. Mink spent 5–20 sec under water when fishing; prey had usually previously been located from an aerial vantage point. Predatory behaviour was highly organized sequentially whereas fish were more prone to indulge in unpredictable stratagems; the behaviour of mink and fish were highly correlated.
The mink's efficiency in catching fish was related to prey size (smaller individuals being more vulnerable to capture) and shoaling. Minnows, which form highly organized shoals, were less easily caught when present in large numbers; this was not true of a loosely shoaling species, the carp.
Of the three species of prey presented, vulnerability to capture took the form goldfish> carp> minnow; these differences, however, may have been influenced by the fish's previous experience of underwater predators.     

The influence of prey size and abundance, and individual phenotype on prey choice by the three-spined stickleback, Gasterosteus aculeatm L.

Prey selection behaviour of three-spined sticklebacks, Gasterosteus aculeatus L., was studied in two experiments. Where possible, the experimental apparatus satisfied the assumptions of the simplest optimal diet model (the basic prey model); prey were presented sequentially, the fish could not search for and handle prey at the same time, and net energy gain, handling time and encounter rate were fixed. Experiment 1 presented fish with a range of Asellus sizes so that pursuit ( p ) and handling ( h ) time could be related to prey size. Published energy values of Asellus together with pursuit and handling times were used to calculate E /( p+h ) for Asellus measuring 3,4,5,6,7 and 9 mm. Pursuit times did not differ with prey size but handling times did. E /( p+h ) was very variable particularly at the larger prey sizes. Experiment 2 presented fish with two sequences of prey differing in the encounter rate with the most profitable prey sizes. Fish did not select the diet predicted by the basic prey model tending to always ignore the largest prey even when net energy gain would have been maximized by including them in the diet. Further analysis showed that the probability of a prey size being taken was a function of prey size, fish stomach fullness and encounter rate. It is concluded that the basic prey model is too simple to capture the behaviour of the fish. One of its main faults is that the changing state of the fish through the feeding bout is ignored.     

Foraging ecology of the Great Crested Grebe (Podiceps cristatus L.) at a mesotrophic-eutrophic reservoir

The foraging ecology of the Great Crested Grebe wasstudied at Dobczyce Reservoir in southernPoland. The mean diving frequency of grebes withoutyoung was 19.3 h^–1, while grebes with young dived onaverage 32.5 h^–1. The mean number of apparent prey caughtby grebes without young was 0.5 fish h^–1. Birds with young caught a greater number, on average4.5 fish h^–1. Probably, birds fishing forthemselves ate much prey underwater. The total lengthof the fish consumed by adult grebes was on average10.0 cm. Adults ate larger fish in the breeding seasonthan in the autumn migration period. Young birds werefed fish about 8.3 cm long. More than 50% of preywere bleak. The mean success of dives of birds withoutyoung was 3.3% and for individuals with young 14.8%.A comparison of the weight of the daily food demandwith the weight of fish brought to the surface showed that it was 70% lower than the dailyfood demand. The poor relation between prey size anddiving success shows that grebes can eat both small andlarge fish below the water surface.     

Foraging in precocial chicks of the black-tailed godwit Limosa limosa: vulnerability to weather and prey size

Self-feeding precocial development is associated with high energy requirements and potentially vulnerable to short-term reductions in food availability, yet few studies have investigated development of foraging in precocial chicks and its sensitivity to environmental conditions. We studied time budgets and foraging behaviour during the 25-d prefledging period in the insectivorous chicks of a grassland shorebird, the black-tailed godwit Limosa limosa . Until 8–10  d old, parental brooding was the main determinant of chicks' daily foraging time. Brooding decreased with age and temperature and increased during rainfall. Foraging time increased to 70–90% of the daylight period in chicks older than a week, during which distances of 3–12  km  d⁻¹ were covered. Chicks took 98% of their arthropod prey from the grassland vegetation. Prey ingestion rates increased in the first week and slowly declined thereafter, modified by wind speed, temperature and time of day. Chicks in poor body condition were brooded more than chicks growing normally and hence had less feeding time, potentially leading to a negative condition spiral under adverse conditions. However, we found no effect of condition on prey ingestion rate that would preclude recovery when conditions improve. Combining behavioural observations with data on energy expenditure revealed that mean prey size was small (1–4.5  mg), necessitating a high feeding rate, but increased notably after 7–10  d of age. This coincided with a decrease in walking speed, suggesting that chicks fed more selectively. Prey of older chicks approached the upper limit of sizes available in exploitable densities in the grassland vegetation, and this enhances the chicks' sensitivity to variation in prey availability due to weather and agricultural practice.     

Optimal foraging as the criteria of prey selection by two centrarchid fishes

The nature of prey selection by two centrarchids (white crappie and bluegill) is presented as a model incorporating optimal foraging strategies. The visual field of the foraging fish as represented by the reactive distance is analysed in detail to estimate the number of prey encounters per search bout. The predicted reactive distances are compared with experimental data. The energetic cost associated with fish foraging behaviour is calculated based on the sequence of events that takes place for each prey consumed. Comparisons of the relative abundance of prey species and size categories in the stomach to the lake environment indicated that both white crappie and bluegill (length < 100 mm) strongly select prey utilising an energy optimization strategy. In most cases, the fish exclusively selected large Daphnia ignoring evasive prey types (Cyclops, Diaptomids) and small cladocera. This selectivity is the result of fish actively avoiding prey with high evasion capabilities even though they appear to be high in energetic content and having translated this into optimal selectivity through capture success rates. The energy consideration and visual system, apart from the forager's ability to capture prey, are the major determinants of prey selectivity for large-sized bluegill and white crappie still at planktivorous stages.     

DIET OF SOUTH AMERICAN FUR SEALS (ARCTOCEPHALUS AUSTRALIS) IN ISLA DE LOBOS, URUGUAY

The diet of Arctocephalus australis was studied through fecal analysis, from September of 1995 to May of 1998, in Isla de Lobos (35°01'50"S-54°53'00"W), Uruguay. A total of 539 scats analyzed indicated that the weakfish ( Cynoscion guatucupa ), the cutlasfish ( Trichiurus lepturus ), the anchoveta ( Engraulis anchoita ), the anchovy ( Anchoa marinii ), and cephalopods were the main prey consumed by these fur seals. Prey richness was higher during January. The diet of A. australis varied between years, apparently related to changes in prey availability. C. guatucupa and E. anchoita decreased while T. lepturus and cephalopods increased from 1996 to 1998. South American fur seals fed on fish ranging in length from 5.4 to 104.8 cm and from 0.7 to 629.9 g in wet mass. However, the mean mass of the main items was never more than 200 g. Observations suggests that A. australis is a trophic generalist with the potential to prey on a wide range of species, although most of the diet is comprised of relatively few species. Fur seals and artisan fisheries both took C. guatucupa , with fur seals taking younger individuals (1–2 yr) than artisan fisheries (> 3 yr).     

Prey selection by experienced and naive juvenile Atlantic salmon

Both in foraging groups and in a sequential prey encounter context, learning had a visible effect on the pattern of selection for three live prey types ( Ecdyonurus larvae, Hydropsyche larvae, and Gammarus ) by juvenile Atlantic salmon Salmo salar . Compared to wild-caught fish, naive, hatchery-reared fish that had not been exposed to natural prey ate Hydropsyche larvae in a remarkably low proportion, and consumed a higher proportion of Gammarus. Ecdyonurus experienced a high and rather steady predation rate across the experience gradient, but after a short period of experience with live prey the consumption rate for Hydropsyche increased drastically, and that of Gammarus decreased, matching the selection pattern exhibited by wild fish. Individual fish offered prey in a sequential encounter context increased consumption rates of all the prey types as they gained experience, but the improvement was higher for the prey that were less consumed initially. Fish became more selective as they approached satiation, conforming to the prediction of optimal foraging theory that higher predator's energy requirements, as well as low food availability, result in reduced selectivity. The results also suggest that fish from distinct populations can differ in the degree of diet selectivity according to their energetic requirements for growth. The fast learning response of Atlantic salmon parr towards novel prey probably allows fish to maintain a high foraging efficiency when faced with frequent changes in the availability of different prey types.