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Prey Size (prey + size)
Selected AbstractsPrey size of single-prey loaders as an indicator of prey abundanceECOLOGY LETTERS, Issue 1 2000A.I. Houston In this paper I am concerned with the behaviour of seabirds that bring back just one prey item at a time to their young. I use a simple model from central place foraging theory to show that the size of fish that a parent bird brings back may increase or decrease with an increase in the abundance of fish. This means that it may not be possible to use the size of fish that is fed to the young as an indicator of prey abundance. [source] Prey size and ingestion rate in raptors: importance for sex roles and reversed sexual size dimorphismJOURNAL OF AVIAN BIOLOGY, Issue 6 2007Tore Slagsvold Compared to other birds, most raptors take large prey for their size, and feeding bouts are extended. However, ingestion rate has largely been overlooked as a constraint in raptors, foraging and breeding ecology. We measured ingestion rate by offering avian and mammalian prey to eighteen wild raptors temporarily kept in captivity, representing seven species and three orders. Ingestion rate was higher for small than for large prey, higher for mammalian than for avian prey, higher for large than for small raptors, and higher for wide-gaped than for narrow-gaped raptors. Mammalian prey were ingested faster by raptors belonging to species with mainly mammals in their diet than by raptors with mainly birds in their diet, but the drop in ingestion rate with increasing prey size was more rapid for the former than for the latter. We argue that the separate sex roles found in raptors, i.e. the male hunting and the female feeding the young, is a solution of the conflict between the prolonged feeding bouts at the nest, and the benefit of rapid resumption of hunting in general, and rapid return to the previous capture site in particular (the prey size hypothesis). Thus, the sex roles differ more when prey takes longer to feed, i.e. from insects to mammals to birds. We then argue that the reversed sexual size dimorphism in raptors, i.e. smaller males than females, results from a conflict between the benefit of being small during breeding to capture the smallest items with the highest ingestion rate among these agile prey types (mammals and bird), and the benefit of being large outside the breeding season to ensure survival by being able to include large items in the diet when small items are scarce (the ingestion rate hypothesis). This hypothesis explains the observed variation in reversed sexual size dimorphism among raptors in relation to size and type of prey, i.e. increasing RSD from insects to mammals to birds as prey. [source] Survival and growth of selected marine fish larvae first fed with eggs and endotrophic larvae of the sea urchin Paracentrotus lividusAQUACULTURE RESEARCH, Issue 9 2010João Gago Abstract Two sets of experiments were carried out to evaluate the potential of eggs and endotrophic larvae of captive Paracentrotus lividus as alternative live prey for marine fish larvae first feeding. The first consisted in rearing sparids, Diplodus sargus and Sparus aurata, larvae until 15 days after hatching in a recirculation system. Compared with the commonly used live prey , rotifer Brachionus spp. , general lower values of survival and growth were obtained when fish larvae were fed with the alternative live prey. Among these, eggs showed to be the preferred feeding. Broodstock feed showed to play a fundamental role on prey quality and consequent fish larvae survival. In the second set of experiments, the 24-h ingestions of the first feeding larvae in static water were determined for five currently cultured fish larvae species. Except for larger and more predatory Dicentrarchus labrax larvae, there was a trend for higher P. lividus egg ingestion, followed by pre-plutei and prisms. Prey size, colour and movement affected food selection by fish larvae. It is concluded that, in spite of the alternative live prey being readily consumed by all tested fish larvae, they cannot however presently compete with rotifers in marine fish larvae first feeding. [source] Assessing the Potential Impact of Cane Toads on Australian SnakesCONSERVATION BIOLOGY, Issue 6 2003BEN L. PHILLIPS Anecdotal reports suggest that the invasion of toads into an area is followed by dramatic declines in the abundance of terrestrial native frog-eating predators, but quantitative studies have been restricted to nonpredator taxa or aquatic predators and have generally reported minimal impacts. Will toads substantially affect Australian snakes? Based on geographic distributions and dietary composition, we identified 49 snake taxa as potentially at risk from toads. The impact of these feral prey also depends on the snakes' ability to survive after ingesting toad toxins. Based on decrements in locomotor (swimming) performance after ingesting toxin, we estimate the LD50 of toad toxins for 10 of the at-risk snake species. Most species exhibited a similar low ability to tolerate toad toxins. Based on head widths relative to sizes of toads, we calculate that 7 of the 10 taxa could easily ingest a fatal dose of toxin in a single meal. The exceptions were two colubrid taxa (keelbacks [ Tropidonophis mairii] and slatey-grey snakes [ Stegonotus cucullatus]) with much higher resistance to toad toxins (up to 85-fold) and one elapid (swamp snakes [ Hemiaspis signata]) with low resistance but a small relative head size and thus low maximum prey size. Overall, our analysis suggests that cane toads threaten populations of approximately 30% of terrestrial Australian snake species. Resumen: Los sapos (Bufo marinus) son anuros grandes muy tóxicos que fueron introducidos a Australia en 1937. Reportes anecdóticos sugieren que la invasión de sapos a un área es seguida de declinaciones dramáticas en la abundancia de depredadores terrestres nativos que se alimentan de ranas, pero los estudios cuantitativos se han restringido a taxones no depredadores o a depredadores acuáticos y generalmente han indicado impactos mínimos. ¿Los sapos afectarán sustancialmente a las serpientes australianas? Basado en la distribución geográfica y la composición de la dieta, identificamos 49 taxones de serpientes como potencialmente en riesgo por los sapos. El impacto de estas presas también depende de la habilidad de las serpientes para sobrevivir después de ingerir toxinas, estimamos la LD50 de toxinas de sapo para 10 de las especies de serpientes "en riesgo." La mayoría de las especies presentaron la misma poca habilidad para tolerar toxinas de sapo. Tomando en cuenta la anchura del cráneo en relación al tamaño de los sapos, calculamos que 7 de las 10 especies podrían fácilmente ingerir una dosis letal en una sola comida. Las excepciones fueron dos taxones de colúbridos (Tropidonophis mairii y Stegonotus cucullatus) con mucha más resistencia (hasta 85 veces más) a toxinas de sapos y un elápido (Hemiaspis signata) con resistencia baja pero de tamaño cefálico relativamente pequeño (y por lo tanto, tamaño máximo de presa pequeño). En general, nuestro análisis sugiere que los sapos amenazan a 30% de las poblaciones de especies de serpientes terrestres de Australia aproximadamente. [source] Foraging specialisms, prey size and life-history patterns: a test of predictions using sympatric polymorphic Arctic charr (Salvelinus alpinus)ECOLOGY OF FRESHWATER FISH, Issue 1 2008D. Fraser Abstract,,, We use arguments based on optimal foraging theory to predict body size constraints and the consequences of these on a range of life-history traits in three trophic specialist morphs of Arctic charr, Salvelinus alpinus, living in sympatry in Loch Rannoch, Scotland. As predicted, foraging specialists feeding on small prey items with a narrow size range showed evidence of deterministic growth; the ultimate body size of macrobenthos feeders being larger (L, = 238 mm) than that of planktivores (L, = 216 mm). In contrast, the piscivorous morph showed no evidence of reaching a maximal body size. The two size-constrained morphs (benthivores and planktivores) matured earlier and died younger (living for up to 11 and 7 years, respectively, in this study) than did the piscivorous charr which showed continuous growth up to at least 17 years. The pattern of annual reproductive investment in maturing individuals was complex. Planktivores invested in larger eggs than the other two forms, but benthivores produced a greater number of eggs than planktivores, which in turn produced more than piscivores. Planktivorous males had a greater investment in mean testis weight than the other two forms. Lifetime reproductive output was the greatest in the benthivorous charr, intermediate in planktivorous and the lowest in the piscivorous charr when measured either as fecundity or as gonadal weight. We conclude that constraints imposed upon foraging specialists by foraging efficiency is a significant driver of body size and ultimately reproductive investment in gape-limited foraging salmonids. [source] Contrasting Patch Residence Strategy in Two Species of Sit-and-Wait Foragers Under the Same Environment: A Constraint by Life History?ETHOLOGY, Issue 2 2005Tadashi Miyashita The present study explored the significance of life history constraints on patch residence strategy by using two congeneric web spider species living in the same habitat. Nephila maculata had a large body size but had a shorter developmental period compared with N. clavata, indicating that N. maculata should have a greater foraging efficiency to reach maturity and reproduce. Residence time at web-sites in N. maculata was shorter than that in N. clavata, irrespective of the season. However, supplementation of food to N. maculata increased residence time, suggesting that it searches web-sites with higher prey intake. Investment of web materials, an important trait influencing web relocation frequency, was not greater in N. maculata. In addition, microhabitat and prey size did not differ significantly after controlling for the effect of body size. Because N. maculata needs to attain a large body size in a shorter period of time, this species appears to take a risk of moving patches to seek high quality web-sites. [source] THE RELATIONSHIP BETWEEN SEXUAL SIZE DIMORPHISM AND HABITAT USE IN GREATER ANTILLEAN ANOLIS LIZARDSEVOLUTION, Issue 1 2000Marguerite A. Butler Abstract., Sexual size dimorphism (SSD) is the evolutionary result of selection operating differently on the body sizes of males and females. Anolis lizard species of the Greater Antilles have been classified into ecomorph classes, largely on the basis of their structural habitat (perch height and diameter). We show that the major ecomorph classes differ in degree of SSD. At least two SSD classes are supported: high SSD (trunk-crown, trunk-ground) and low SSD (trunk, crown-giant, grass-bush, twig). Differences cannot be attributed to an allometric increase of SSD with body size or to a phylogenetic effect. A third explanation, that selective pressures on male and/or female body size vary among habitat types, is examined by evaluating expectations from the major relevant kinds of selective pressures. Although no one kind of selective pressure produces expectations consistent with all of the information, competition with respect to structural habitat and sexual selection pressures are more likely possibilities than competition with respect to prey size or optimal feeding pressures. The existence of habitat-specific sexual dimorphism suggests that adaptation of Anolis species to their environment is more complex than previously appreciated. [source] Size-dependent predation risk in tree-feeding insects with different colouration strategies: a field experimentJOURNAL OF ANIMAL ECOLOGY, Issue 5 2009Triinu Remmel Summary 1. Body size is positively correlated with fecundity in various animals, but the factors that counterbalance the resulting selection pressure towards large size are difficult to establish. Positively size-dependent predation risk has been proposed as a selective factor potentially capable of balancing the fecundity advantage of large size. 2. To construct optimality models of insect body size, realistic estimates of size-dependent predation rates are necessary. Moreover, prey traits such as colouration should be considered, as they may substantially alter the relationship between body size and mortality risk. 3. To quantify mortality patterns, we conducted field experiments in which we exposed cryptic and conspicuous artificial larvae of different sizes to bird predators, and recorded the incidence of bird attacks. 4. The average daily mortality rate was estimated to vary between 4% and 10%. In both cryptic and conspicuous larvae, predation risk increased with prey size, but the increase tended to be steeper in the conspicuous group. No main effect of colour type was found. All the quantitative relationships were reasonably consistent across replicates. 5. Our results suggest that the size dependence of mortality risk in insect prey is primarily determined by the probability of being detected by a predator rather than by a size-dependent warning effect associated with conspicuous colouration. Our results therefore imply that warningly coloured insects do not necessarily benefit more than the cryptic species from large body size, as has been previously suggested. [source] Predator size, prey size and threshold food densities of diving ducks: does a common prey base support fewer large animals?JOURNAL OF ANIMAL ECOLOGY, Issue 5 2009Samantha E. Richman Summary 1. Allometry predicts that a given habitat area or common prey biomass supports fewer numbers of larger than smaller predators; however, birds from related taxa or the same feeding guild often deviate from this pattern. In particular, foraging costs of birds may differ among locomotor modes, while intake rates vary with accessibility, handling times and energy content of different-sized prey. Such mechanisms might affect threshold prey densities needed for energy balance, and thus relative numbers of different-sized predators in habitats with varying prey patches. 2. We compared the foraging profitability (energy gain minus cost) of two diving ducks: smaller lesser scaup (Aythya affinis, 450,1090 g) and larger white-winged scoters (Melanitta fusca, 950,1800 g). Calculations were based on past measurements of dive costs with respirometry, and of intake rates of a common bivalve prey ranging in size, energy content and burial depth in sediments. 3. For scaup feeding on small prey <12 mm long, all clams buried deeper than 5 cm were unprofitable at realistic prey densities. For clams buried in the top 5 cm, the profitability threshold decreased from 216 to 34 clams m,2 as energy content increased from 50 to 300 J clam,1. 4. For larger scoters feeding on larger prey 18,24 mm long, foraging was profitable for clams buried deeper than 5 cm, with a threshold density of 147 m,2 for clams containing 380 J clam,1. For clams <5 cm deep, the threshold density decreased from 86 to 36 clams m,2 as energy content increased from 380 to 850 J clam,1. If scoters decreased dive costs by swimming with wings as well as feet (not an option for scaup), threshold prey densities were 11,12% lower. 5. Our results show that threshold densities of total prey numbers for different-sized ducks depend on prey size structure and depth in the sediments. Thus, heterogeneity in disturbance regimes and prey population dynamics can create a mosaic of patches favouring large or small predators. Whether a given area or total prey biomass will support greater numbers of larger or smaller predators will vary with these effects. [source] The role of prey size and abundance in the geographical distribution of spider socialityJOURNAL OF ANIMAL ECOLOGY, Issue 5 2007KIMBERLY S. POWERS Summary 1Social species in the spider genus Anelosimus predominate in lowland tropical rainforests, while congeneric subsocial species occur at higher elevations or higher latitudes. 2We conducted a comparative study to determine whether differences in total biomass, insect size or both have been responsible for this pattern. 3We found that larger average insect size, rather than greater overall biomass per se, is a key characteristic of lowland tropical habitats correlating with greater sociality. 4Social species occupied environments with insects several times larger than the spiders, while subsocial species nearing dispersal occupied environments with smaller insects in either high or low overall biomass. 5Similarly, in subsocial spider colonies, individuals lived communally at a time when they were younger and therefore smaller than the average insect landing on their webs. 6We thus suggest that the availability of large insects may be a critical factor restricting social species to their lowland tropical habitats. [source] The role of trout in stream food webs: integrating evidence from field surveys and experimentsJOURNAL OF ANIMAL ECOLOGY, Issue 2 2006KRISTIAN MEISSNER Summary 1We evaluated the effects of brown trout on boreal stream food webs using field surveys and enclosure/exclosure experiments. Experimental results were related to prey preference of uncaged trout in the same stream, as well as to a survey of macroinvertebrate densities in streams with vs. without trout. Finally, we assessed the generality of our findings by examining salmonid predation on three groups of macroinvertebrate prey (chironomid midges, epibenthic grazers, invertebrate predators) in a meta-analysis. 2In a preliminary experiment, invertebrate predators showed a strong negative response to trout, whereas chironomids benefited from trout presence. In the main experiment, trout impact increased with prey size. Trout had the strongest effect on invertebrate predators and cased caddis larvae, whereas Baetis mayfly and chironomid larvae were unaffected. Trout impact on the largest prey seemed mainly consumptive, because prey emigration rates were low and independent of fish presence. Despite strong effects on macroinvertebrates, trout did not induce a trophic cascade on periphyton. Uncaged trout showed a strong preference for the largest prey items (predatory invertebrates and aerial prey), whereas Baetis mayflies and chironomids were avoided by trout. 3Densities of invertebrate predators were significantly higher in troutless streams. Baetis mayflies also were less abundant in trout streams, whereas densities of chironomids were positively, although non-significantly, related to trout presence. Meta-analysis showed a strong negative impact of trout on invertebrate predators, a negative but variable impact on mobile grazers (mainly mayfly larvae) and a slightly positive impact on chironomid larvae. 4Being size-selective predators, salmonid fishes have a strong impact on the largest prey types available, and this effect spans several domains of scale. Discrepancies between our experimental findings and those from the field survey and meta-analysis show, however, that for most lotic prey, small-scale experiments do not reflect fish impact reliably at stream-wide scales. 5Our findings suggest that small-scale experiments will be useful only if the experimental results are evaluated carefully against natural history information about the experimental system and interacting species across a wide array of spatial scales. [source] When time is of the essence: choosing a currency for prey-handling costsJOURNAL OF ANIMAL ECOLOGY, Issue 4 2000Francesco Rovero 1.,Heartbeat rate was measured in shore crabs Carcinus maenas (L.) feeding on mussels Mytilus edulis L. in order to estimate the energetic cost of handling prey and to assess the relative importance of energy and time as costing currencies. 2.,Energetic handling costs represented approximately 2% of corresponding gains. 3.,The tendency of profitability (gain per unit handling time) to increase with prey size was weakened by including energetic handling costs. 4.,Time was judged to be a more appropriate currency than energy for costing prey-handling behaviour. 5.,The importance of time as a costing currency, either through the principle of lost opportunity or through exposure to mortality risk, may extend to other behavioural systems, including aggression. [source] Influence of prey size on predation success by Zelus longipes L. (Het., Reduviidae)JOURNAL OF APPLIED ENTOMOLOGY, Issue 2-3 2002R. Cogni The effects of prey size on the predatory responses of the reduviid Zelus longipes were studied through laboratory tests using larvae of the noctuid moth Spodoptera frugiperda as preys. In tests with one caterpillar, larvae of three different weight classes were offered individually to the predator. The prey weight was positively correlated with relative weight gain by the predator, mean feeding time and discarded biomass, but not with the relative extraction rate (defined as the relative weight gain by the predator by feeding time). The different sizes of caterpillars were attacked with the same frequency, but the successful attacks were more frequent in small larvae. The median mass of successfully attacked larvae was also less than that of unsuccessfully attacked. In tests with three caterpillars, larvae of three weight classes were offered at the same time; small caterpillars were more often attacked and killed than the medium and large ones. The results showed that even if larger preys resulted in more energy intake, when the choice is possible, smaller caterpillars were more likely to be attacked than medium and large. This is probably related to the fact that successful attacks were more frequent in small larvae, and also reduced the risk of injury to the predator. [source] Observations on feed size and capture success in the larval butterfly splitfin (Ameca splendens Miller & Fitzsimons, 1971, Pisces: Goodeidae) reared on zooplanktonJOURNAL OF APPLIED ICHTHYOLOGY, Issue 3 2007F. Peña-Aguado Summary In this study, we quantified the feeding behaviour (encounter, attack, capture. and ingestion) of larval A. splendens on micro-crustacean prey [cladocerans: Alona rectangula, Simocephalus vetulus (separately neonates and adults), Ceriodaphnia dubia, Daphnia pulex (juveniles), Moina macrocopa and ostracods: Heterocypris incongruens]. Although we initially (first 4 weeks) offered rotifers (Brachionus calyciflorus and B. patulus), they were not consumed by the larvae and hence observations with these prey were discontinued. Feeding behaviour was observed during the first 10 weeks. Fifteen observations were made with each prey species (seven diets × four replicates). Experiments were conducted in 50 ml transparent containers with 20 ml fish-conditioned water into which one fry was introduced. Before introducing the fish, 20 individuals of a given cladoceran prey species or 50 individuals of a rotifer prey species were introduced. Until the fourth week, we used 20 ml of medium and thereafter 30 ml, but the prey density used remained constant (1 ind. ml,1). Observations (10 min per fry per cladoceran replicate) were taken under a stereomicroscope (20×) for the first 2 weeks and later with a lamp and a magnifying lens. The number of encounters (E), attacks (A), captures (C) and ingestions (I) were recorded. During the study period, there was a 60% increase in gape size but only a 30% increase in body length. The number of encounters of larval A. splendens was highest (192) on M. macrocopa and lowest (29) on ostracods and adult S. vetulus (59). The inverse relationship between capture success and prey size was more pronounced during the latter half of the study period. Compared with all the other prey types offered, A. splendens fed maximally on M. macrocopa, which therefore could be a suitable diet for the larval rearing of this fish species. [source] Prey size and ingestion rate in raptors: importance for sex roles and reversed sexual size dimorphismJOURNAL OF AVIAN BIOLOGY, Issue 6 2007Tore Slagsvold Compared to other birds, most raptors take large prey for their size, and feeding bouts are extended. However, ingestion rate has largely been overlooked as a constraint in raptors, foraging and breeding ecology. We measured ingestion rate by offering avian and mammalian prey to eighteen wild raptors temporarily kept in captivity, representing seven species and three orders. Ingestion rate was higher for small than for large prey, higher for mammalian than for avian prey, higher for large than for small raptors, and higher for wide-gaped than for narrow-gaped raptors. Mammalian prey were ingested faster by raptors belonging to species with mainly mammals in their diet than by raptors with mainly birds in their diet, but the drop in ingestion rate with increasing prey size was more rapid for the former than for the latter. We argue that the separate sex roles found in raptors, i.e. the male hunting and the female feeding the young, is a solution of the conflict between the prolonged feeding bouts at the nest, and the benefit of rapid resumption of hunting in general, and rapid return to the previous capture site in particular (the prey size hypothesis). Thus, the sex roles differ more when prey takes longer to feed, i.e. from insects to mammals to birds. We then argue that the reversed sexual size dimorphism in raptors, i.e. smaller males than females, results from a conflict between the benefit of being small during breeding to capture the smallest items with the highest ingestion rate among these agile prey types (mammals and bird), and the benefit of being large outside the breeding season to ensure survival by being able to include large items in the diet when small items are scarce (the ingestion rate hypothesis). This hypothesis explains the observed variation in reversed sexual size dimorphism among raptors in relation to size and type of prey, i.e. increasing RSD from insects to mammals to birds as prey. [source] How different provisioning strategies result in equal rates of food delivery: an experimental study of blue tits Parus caeruleusJOURNAL OF AVIAN BIOLOGY, Issue 4 2002Fabrizio Grieco Food provisioning in birds requires a considerable amount of time and usually has to be traded-off against other parental and non-parental activities. I investigated experimentally the rate at which blue tit Parus caeruleus parents deliver food to their brood after a change in food availability. The main argument behind this study is that parents enjoying an additional food source may use less time for self-feeding and therefore use more time for food provisioning. This could increase the rate at which food is brought to the nest. However, a prey choice model that takes the energetic needs of the parent into account allows for the possibility that the food-supplemented parents would deliver the same amount of food by increasing prey size (through an increase in prey selectivity) and reducing visit rate. The field data indicate that the parents changed provisioning strategy when food-supplemented: they fed the chicks natural food less frequently, but brought larger larvae. On the whole, delivery rate of natural food was the same or lower than in controls. The results suggest that food-supplemented parents used the time saved to increase their degree of food selectivity. When the gains from an increased delivery rate are not worth the increased costs (mainly resulting from an increased visiting rate), the parent with low energetic need may increase selectivity to provide the same amount of food to the brood as the unmanipulated parent, but at a lower cost. [source] Musculoskeletal underpinnings to differences in killing behavior between North American accipiters (Falconiformes: Accipitridae) and falcons (Falconidae)JOURNAL OF MORPHOLOGY, Issue 3 2008Diego Sustaita Abstract Accipiters (Accipiter spp.) and falcons (Falco spp.) both use their feet to seize prey, but falcons kill primarily with their beaks, whereas accipiters kill with their feet. This study examines the mechanistic basis to differences in their modes of dispatching prey, by focusing on the myology and biomechanics of the jaws, digits, and distal hindlimb. Bite, grip, and distal hindlimb flexion forces were estimated from measurements of physiological cross-sectional area (PCSA) and indices of mechanical advantage (MA) for the major jaw adductors, and digit and tarsometatarsal flexors. Estimated bite force, total jaw adductor PCSA, and jaw MA (averaged over adductors) tended to be relatively and absolutely greater in falcons, reflecting their emphasis on biting for dispatching their prey. Differences between genera in estimated grip force, total digit flexor PCSA, and digit MA (averaged over inter-phalangeal joints and digits) were not as clear-cut; each of these parameters scaled positively allometric in accipiters, which may reflect the scaling of both prey size, and the proportion of mammalian prey consumed by this lineage with increasing body size. Estimated tarsometatarsal force was greater in falcons than in accipiters, due to their greater MA, which may reflect selection for incurring greater forces during prey strikes. Conversely, the comparatively lower tarsometatarsal MA in accipiters reflects their capacity for greater foot speed potentially necessary for grasping elusive prey. Thus, this study elucidates how differences in jaw and hindlimb musculoskeletal morphology of accipiters and falcons are reflected in differences in their killing modes, and through differences in their force-generating capacities. J. Morphol., 2008. © 2007 Wiley-Liss, Inc. [source] Factors affecting the predation of otter (Lutra lutra) on European pond turtle (Emys orbicularis)JOURNAL OF ZOOLOGY, Issue 2 2006J. Lanszki Abstract In this case study, the ecological background of an unusual hunting behaviour was investigated, when otters Lutra lutra preyed upon European pond turtles Emys orbicularis in a Hungarian fish pond system during an 18-month period. Predation on turtle was found only during cold periods (established by spraint analysis and also by the collection of 182 turtle carcasses in 2003). The relationship was not close between fish availability and turtle consumption (rP=,0.325, P=0.19). The crude protein content of the turtle head and leg was higher than that of fish, frog and turtle body, whereas the energy content of the samples was similar. The mean body weight of the killed turtles (460 g) fell within the range of the optimal prey size of the otter. Turtles were used as cache foods by otters during extreme environmental conditions (as in the long winter), but occurred only rarely as buffer foods during moderate winter. In fish ponds, the conservation of the coexistent otter and turtle depends on pond management. The maintenance of a higher fish availability in ponds during winter makes it possible to avoid the need to acquire a proper hunting technique on turtle, indicated by the scarcity of primary fish food. [source] DIET OF HARBOR PORPOISES IN THE KATTEGAT AND SKAGERRAK SEAS: ACCOUNTING FOR INDIVIDUAL VARIATION AND SAMPLE SIZEMARINE MAMMAL SCIENCE, Issue 1 2003Patrik Börjesson Abstract Stomach contents of 112 bycaught harbor porpoises (Phocoena phocoena) collected between 1989 and 1996 in the Kattegat and Skagerrak seas were analyzed to describe diet composition and estimate prey size, to examine sample size requirements, and to compare juvenile and adult diets. Although porpoises preyed on a variety of species, only a few contributed substantially to the diet. Atlantic herring (Clupea harengus) was the dominating prey species for both juveniles and adults. Our results, in combination with those from previous studies, suggest that where herring is a dominant food source, porpoises prey primarily on size classes containing mature or maturing individuals. Further, we also show that Atlantic hagfish (Myxine glutinosa) may be an important food resource, at least for adult porpoises. Examination of sample size requirement showed that, depending on the taxonomic level used to describe the diet, a minimum of 35,71 stomachs are needed to be confident that all common prey species will be found. [source] Active selection for large guppies, Poecilia reticulata, by the pike cichlid, Crenicichla saxatilisOIKOS, Issue 3 2004Jan Johansson Size-selective predation has been proposed to be one important evolutionary force shaping life-history traits in guppies (Poecilia reticulata). Populations living in the presence of the ring-tailed pike cichlid (Crenicichlasaxatilis) are smaller, mature earlier, allocate more energy to offspring and get more and smaller young than guppies in localities without Crenicichla. We investigated if Crenicichlasaxatilis is a size-selective predator, if the selectivity is a result of active choice and if the optimal prey size can be explained according to an optimal foraging model. In single-prey experiments we quantified the predators' pre-capture costs (time), capture success, and post-capture costs (time) for four different prey sizes spanning from 10 to 40 mm total length. To see which of the components of the prey cycle the predator takes into account for its choice, we then predicted prey values and optimal prey size with 6 different models that included one or more of the prey cycle components. In two multiple prey experiments, the cichlids were given the choice of the two and four different prey sizes simultaneously. Crenicichlasaxatilis actively selected the largest guppies in both cases. The three prey-value functions that included handling time (post-capture cost) did not accurately predict the prey choice. Instead the prey-value functions that took into account pre-capture cost (approach and attack time) were able to correctly predict the choice of the largest guppy size, suggesting that pre-capture costs may be more important than post-capture costs for prey choice in Crenicichlasaxatilis. The study confirms that Crenicichlasaxatilis is a size-selective predator selecting large guppies, while earlier evidence for selectivity for large prey in Crenicichla cichlids has been weak and equivocal. Our result strengthen the possibility that size-selective predation is a mechanism in life-history evolution in guppies. [source] Improved techniques for rearing mud crab Scylla paramamosain (Estampador 1949) larvaeAQUACULTURE RESEARCH, Issue 14 2007Truong Trong Nghia Abstract A series of rearing trials in small 1 L cones and large tanks of 30,100 L were carried out to develop optimal rearing techniques for mud crab (Scylla paramamosain) larvae. Using water exchange (discontinuous partial water renewal or continuous treatment through biofiltration) and micro-algae (Chlorella or Chaetoceros) supplementation (daily supplementation at 0.1,0.2 million cells mL,1 or maintenance at 1,2 millions cells mL,1), six different types of rearing systems were tried. The combination of a green-water batch system for early stages and a recirculating system with micro-algae supplementation for later stages resulted in the best overall performance of the crab larvae. No clear effects of crab stocking density (50,200 larvae L,1) and rotifer (30,60 rotifers mL,1) and Artemia density (10,20 L,1) were observed. A stocking density of 100,150 zoea 1 (Z1) L,1, combined with rotifer of 30,45 mL,1 for early stages and Artemia feeding at 10,15 nauplii mL,1 for Z3,Z5 seemed to produce the best performance of S. paramamosain larvae. Optimal rations for crab larvae should, however, be adjusted depending on the species, larval stage, larval status, prey size, rearing system and techniques. A practical feeding schedule could be to increase live food density from 30 to 45 rotifers mL,1 from Z1 to Z2 and increase the number of Artemia nauplii mL,1 from 10 to 15 from Z3 to Z5. Bacterial disease remains one of the key factors underlying the high mortality in the zoea stages. Further research to develop safe prophylactic treatments is therefore warranted. Combined with proper live food enrichment techniques, application of these findings has sustained a survival rate from Z1 to crab 1,2 stages in large rearing tanks of 10,15% (maximum 30%). [source] Craniodental indicators of prey size preference in the FelidaeBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 4 2009JULIE MEACHEN-SAMUELS In the present study, we used linear morphometrics of the crania, mandible and dentition to explore the association between craniodental shape and prey size among 35 species of living felids. To accomplish this, felids were divided into three prey-size groups: (1) large prey specialists; (2) small prey specialists; and (3) mixed prey feeders. From these linear measurements, large prey specialist felids can be distinguished from small and mixed prey feeders by their relatively robust canines and incisors and relatively wide muzzles. These cranial characters are advantageous when dispatching large prey, due to the stranglehold that cats employ during this activity. Robust canines resist the bending and torsional forces applied by struggling prey and a wider muzzle helps to stabilize grip and distribute bite forces more evenly during the killing bite. Small prey specialists had smaller canines, narrower muzzles and slightly longer jaws for a speed advantage when catching small, quick prey. Mixed prey feeders were intermediate between large and small prey specialists, indicating they are adapted to killing both sizes of prey. Given the success of this ecomorphological analysis of living felids that specialize on different prey sizes, we look forward to applying this same approach to extinct species. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 96, 784,799. [source] Prey size selection in piscivorous pikeperch (Stizostedion lucioperca) includes active prey choiceECOLOGY OF FRESHWATER FISH, Issue 4 2002H. Turesson Abstract,,,Knowledge of the mechanisms behind prey selection in piscivorous fish is important for our understanding of the dynamics of freshwater systems. Prey selection can involve active predator choice or be a passive process. We experimentally studied size-selectivity in pikeperch, feeding on roach and rudd. When given a choice of different prey sizes, pikeperch selected small prey. Passive selection mechanisms (encounter rate, capture success and satiation) could not fully explain the pattern of diet choice. Instead, behavioural analysis revealed that the pikeperch actively selected small-sized prey. Optimal foraging theory, predicting that predators will choose prey sizes giving highest energy return per time spent foraging, is assumed to explain active choice. We measured handling times for a range of prey sizes and found that the most profitable sizes were also the chosen ones, both in experiments and in the field. This suggests that pikeperch choose their prey to maximise energy intake per unit time. [source] Ecological processes influencing mortality of juvenile pink salmon (Oncorhynchus gorbuscha) in Prince William Sound, AlaskaFISHERIES OCEANOGRAPHY, Issue 2001T. M. Willette Abstract Our collaborative work focused on understanding the system of mechanisms influencing the mortality of juvenile pink salmon (Oncorhynchus gorbuscha) in Prince William Sound, Alaska. Coordinated field studies, data analysis and numerical modelling projects were used to identify and explain the mechanisms and their roles in juvenile mortality. In particular, project studies addressed the identification of major fish and bird predators consuming juvenile salmon and the evaluation of three hypotheses linking these losses to (i) alternative prey for predators (prey-switching hypothesis); (ii) salmon foraging behaviour (refuge-dispersion hypothesis); and (iii) salmon size and growth (size-refuge hypothesis). Two facultative planktivorous fishes, Pacific herring (Clupea pallasi) and walleye pollock (Theragra chalcogramma), probably consumed the most juvenile pink salmon each year, although other gadids were also important. Our prey-switching hypothesis was supported by data indicating that herring and pollock switched to alternative nekton prey, including juvenile salmon, when the biomass of large copepods declined below about 0.2 g m,3. Model simulations were consistent with these findings, but simulations suggested that a June pteropod bloom also sheltered juvenile salmon from predation. Our refuge-dispersion hypothesis was supported by data indicating a five-fold increase in predation losses of juvenile salmon when salmon dispersed from nearshore habitats as the biomass of large copepods declined. Our size-refuge hypothesis was supported by data indicating that size- and growth-dependent vulnerabilities of salmon to predators were a function of predator and prey sizes and the timing of predation events. Our model simulations offered support for the efficacy of representing ecological processes affecting juvenile fishes as systems of coupled evolution equations representing both spatial distribution and physiological status. Simulations wherein model dimensionality was limited through construction of composite trophic groups reproduced the dominant patterns in salmon survival data. In our study, these composite trophic groups were six key zooplankton taxonomic groups, two categories of adult pelagic fishes, and from six to 12 groups for tagged hatchery-reared juvenile salmon. Model simulations also suggested the importance of salmon density and predator size as important factors modifying the predation process. [source] Large predators and their prey in a southern African savanna: a predator's size determines its prey size rangeJOURNAL OF ANIMAL ECOLOGY, Issue 3 2004Frans G. T. Radloff Summary 1A long-term (13-year) data set, based on > 4000 kills, was used to test whether a sympatric group of large predators adheres to the theoretical predictions that (1) mean prey body size and (2) prey diversity increase as functions of predator body size. 2All kills observed by safari guides are documented routinely in Mala Mala Private Game Reserve, South Africa. We analysed these records for lion (Panthera leo, Linnaeus), leopard (Panthera pardus, Linnaeus), cheetah (Acinonyx jubatus, Schreber) and African wild dog (Lycaon pictus, Temminck). Males and females of the sexually dimorphic felid species were treated as functionally distinct predator types. Prey types were classified by species, sex and age class. 3Prey profiles were compared among predator types in terms of richness and evenness to consider how both the range of prey types used and the dominance of particular prey types within each range may be influenced by predator size. No significant size-dependent relationships were found, so factors separate from or additional to body size must explain variation in prey diversity across sympatric predators. 4A statistically strong relationship was found between mean prey mass and predator mass (r2 = 0·86, P= 0·002), although pairwise comparisons showed that most predators killed similar prey despite wide differences in predator size. Also, minimum prey mass was independent of predator mass while maximum prey mass was strongly dependent on predator mass (r2 = 0·71, P= 0·017). The ecological significance is that larger predators do not specialize on larger prey, but exploit a wider range of prey sizes. [source] Active selection for large guppies, Poecilia reticulata, by the pike cichlid, Crenicichla saxatilisOIKOS, Issue 3 2004Jan Johansson Size-selective predation has been proposed to be one important evolutionary force shaping life-history traits in guppies (Poecilia reticulata). Populations living in the presence of the ring-tailed pike cichlid (Crenicichlasaxatilis) are smaller, mature earlier, allocate more energy to offspring and get more and smaller young than guppies in localities without Crenicichla. We investigated if Crenicichlasaxatilis is a size-selective predator, if the selectivity is a result of active choice and if the optimal prey size can be explained according to an optimal foraging model. In single-prey experiments we quantified the predators' pre-capture costs (time), capture success, and post-capture costs (time) for four different prey sizes spanning from 10 to 40 mm total length. To see which of the components of the prey cycle the predator takes into account for its choice, we then predicted prey values and optimal prey size with 6 different models that included one or more of the prey cycle components. In two multiple prey experiments, the cichlids were given the choice of the two and four different prey sizes simultaneously. Crenicichlasaxatilis actively selected the largest guppies in both cases. The three prey-value functions that included handling time (post-capture cost) did not accurately predict the prey choice. Instead the prey-value functions that took into account pre-capture cost (approach and attack time) were able to correctly predict the choice of the largest guppy size, suggesting that pre-capture costs may be more important than post-capture costs for prey choice in Crenicichlasaxatilis. The study confirms that Crenicichlasaxatilis is a size-selective predator selecting large guppies, while earlier evidence for selectivity for large prey in Crenicichla cichlids has been weak and equivocal. Our result strengthen the possibility that size-selective predation is a mechanism in life-history evolution in guppies. [source] Decreasing trophic efficiency in cool-water aquaculture ponds: size-selective predation removes large preyAQUACULTURE RESEARCH, Issue 5 2009Chelsea O Bennice Abstract Maximizing young-of-year (YOY) fish production in an aquaculture setting depends on matching predatory demand with prey availability. With a size-selective YOY fish species (saugeye: Sander vitreus Mitchell females ×S. canadense Griffith & Smith males) supplied with natural zooplankton prey (Bosmina sp. Baird), selective removal of larger individuals may decrease prey fecundity. However, increased nutrient fertilization may also ameliorate the top-down effects of fish predation. We tested these interactions in outdoor earthen production ponds (ca. 4000 m2; n=12) by measuring Bosmina sp. size at first reproduction (SFR), maximum size (MAX) and neonate size (NEO) in ponds that varied in YOY saugeye densities (18,50 saugeye m,3) and also differed in phosphorus maintenance levels (either 20 or 30 ,g PO4 -P L,1). We found that SFR decreased by 8% [from 0.298 mm±0.007 (mean±1 SE) to 0.275 mm±0.005], MAX decreased by 11% (from 0.367 mm±0.009 to 0.328 mm±0.009) and NEO decreased by 5% (0.198 mm±0.004 to 0.189 mm±0.003) over the range of saugeye densities, and that SFR increased by 4% (from 0.279 mm±0.004 to 0.290 mm±0.003) and MAX increased by 3% (from 0.336 mm±0.004 to 0.347±0.004) with increased fertilization. Further, prey offspring lengths strongly related to mother lengths and lengths differed from early to late in the production season. These results indicate that multiple factors affect prey sizes and emphasize that the removal of large prey individuals by size-selective YOY predators may decrease trophic efficiency, ultimately decreasing fish production. [source] Craniodental indicators of prey size preference in the FelidaeBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 4 2009JULIE MEACHEN-SAMUELS In the present study, we used linear morphometrics of the crania, mandible and dentition to explore the association between craniodental shape and prey size among 35 species of living felids. To accomplish this, felids were divided into three prey-size groups: (1) large prey specialists; (2) small prey specialists; and (3) mixed prey feeders. From these linear measurements, large prey specialist felids can be distinguished from small and mixed prey feeders by their relatively robust canines and incisors and relatively wide muzzles. These cranial characters are advantageous when dispatching large prey, due to the stranglehold that cats employ during this activity. Robust canines resist the bending and torsional forces applied by struggling prey and a wider muzzle helps to stabilize grip and distribute bite forces more evenly during the killing bite. Small prey specialists had smaller canines, narrower muzzles and slightly longer jaws for a speed advantage when catching small, quick prey. Mixed prey feeders were intermediate between large and small prey specialists, indicating they are adapted to killing both sizes of prey. Given the success of this ecomorphological analysis of living felids that specialize on different prey sizes, we look forward to applying this same approach to extinct species. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 96, 784,799. [source] |