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Predation Events (predation + event)
Selected AbstractsTemperature-sensing telemetry , possibilities for assessing the feeding ecology of marine mammals and their potential impacts on returning salmonid populationsFISHERIES MANAGEMENT & ECOLOGY, Issue 5-6 2008B. BENDALL Abstract, Adult salmonids returning to the River Tees (north-east England) tagged with temperature-sensing acoustic transmitters provided some unexpected and novel information on the possible impact of seal predation at a tidal barrage 16 km from the sea. Predation events of tagged fish by seals were inferred by an increase in the temperature transmitted by the acoustic tags. Subsequent events of feeding or drinking by the seals were also inferred from further changes in temperature recorded by tags whilst in their stomachs. Rates of inferred predation on tagged individuals were high (47%). This is the first time that temperature-sensing transmitters deployed inside wild salmonids have revealed instances of predation by, and subsequent feeding ecology of, marine mammals. The results are discussed in relation to the use of such technology in future studies attempting to address the interactions between marine mammals and their fish prey species. [source] Interpreting the smells of predation: how alarm cues and kairomones induce different prey defencesFUNCTIONAL ECOLOGY, Issue 6 2009Nancy M. Schoeppner Summary 1.,For phenotypically plastic organisms to produce phenotypes that are well matched to their environment, they must acquire information about their environment. For inducible defences, cues from damaged prey and cues from predators both have the potential to provide important information, yet we know little about the relative importance of these separate sources of information for behavioural and morphological defences. We also do not know the point during a predation event at which kairomones are produced, i.e. whether they are produced constitutively, during prey attack or during prey digestion. 2.,We exposed leopard frog tadpoles (Rana pipiens) to nine predator cue treatments involving several combinations of cues from damaged conspecifics or heterospecifics, starved predators, predators only chewing prey, predators only digesting prey or predators chewing and digesting prey. 3.,We quantified two behavioural defences. Tadpole hiding behaviour was induced only by cues from crushed tadpoles. Reduced tadpole activity was induced only by cues from predators digesting tadpoles or predators chewing + digesting tadpoles. 4.,We also quantified tadpole mass and two size-adjusted morphological traits that are known to be phenotypically plastic. Mass was unaffected by the cue treatments. Relative body length was affected (i.e. there were differences among some treatments), but none of the treatments significantly differed from the no-predator control. Relative tail depth was affected by the treatments and deeper tails were induced only when tadpoles were exposed to cues from predators digesting tadpoles or cues from predators chewing + digesting tadpoles. 5.,These results demonstrate that some prey species can discriminate among a diverse set of potential cues from heterospecific prey, conspecific prey and predators. Moreover, the results illustrate that the cues responsible for the full suite of behavioural and morphological defences are not induced by tadpole crushing nor can they be induced by generalized digestive chemicals produced when predators digest their prey. Instead, both prey damage and predator digestion of conspecific tissues appear to be important for communicating predatory risk to phenotypically plastic anuran prey. Importantly, the production of chemical cues by predators may be unavoidable and prey have evolved the ability to eavesdrop on these signals. [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] Predator functional response and prey survival: direct and indirect interactions affecting a marked prey populationJOURNAL OF ANIMAL ECOLOGY, Issue 1 2006DAVID A. MILLER Summary 1Predation plays an integral role in many community interactions, with the number of predators and the rate at which they consume prey (i.e. their functional response) determining interaction strengths. Owing to the difficulty of directly observing predation events, attempts to determine the functional response of predators in natural systems are limited. Determining the forms that predator functional responses take in complex systems is important in advancing understanding of community interactions. 2Prey survival has a direct relationship to the functional response of their predators. We employed this relationship to estimate the functional response for bald eagle Haliaeetus leucocepalus predation of Canada goose Branta canadensis nests. We compared models that incorporated eagle abundance, nest abundance and alternative prey presence to determine the form of the functional response that best predicted intra-annual variation in survival of goose nests. 3Eagle abundance, nest abundance and the availability of alternative prey were all related to predation rates of goose nests by eagles. There was a sigmoidal relationship between predation rate and prey abundance and prey switching occurred when alternative prey was present. In addition, predation by individual eagles increased as eagle abundance increased. 4A complex set of interactions among the three species examined in this study determined survival rates of goose nests. Results show that eagle predation had both prey- and predator-dependent components with no support for ratio dependence. In addition, indirect interactions resulting from the availability of alternative prey had an important role in mediating the rate at which eagles depredated nests. As a result, much of the within-season variation in nest survival was due to changing availability of alternative prey consumed by eagles. 5Empirical relationships drawn from ecological theory can be directly integrated into the estimation process to determine the mechanisms responsible for variation in observed survival rates. The relationship between predator functional response and prey survival offers a flexible and robust method to advance our understanding of predator,prey interactions in many complex natural systems where prey populations are marked and regularly visited. [source] Nest predators of Lance-tailed Manakins on Isla Boca Brava, PanamáJOURNAL OF FIELD ORNITHOLOGY, Issue 2 2009Jennifer L. Reidy ABSTRACT Nest predation is often the primary cause of nest failure for passerines. Despite this, little is known about predation rates and the nest predators of birds in the tropics. I used video cameras to monitor seven Lance-tailed Manakin (Chiroxiphia lanceolata) nests on Isla Boca Brava, Panamá. One nest fledged young and six nests failed due to predation. I recorded five predation events involving four avian predators and one mammalian predator. Crested Oropendolas (Psarocolius decumanus) predated two nests and a Roadside Hawk (Buteo magnirostris) and a Black-chested Jay (Cyanocorax affinis) each predated one. The mammalian predator was a common opossum (Didelphis marsupialis). All avian predation was diurnal; the mammalian predation was nocturnal. My results suggest that tropical birds are subject to a diverse suite of nest predators, and that avian predators may be an important cause of nest failure at my study site. RESUMEN La depredación de nidos es usualmente la primera causa del fracaso de lo nidos de los paserinos. A pesar de esto, poco se conoce sobre la tasa de depredación y los depredadores de nidos de aves neotropicales. Yo use cámaras de video para monitorear siete nidos del Lance-tailed Manakins (Chiroxiphia lanceolata) en la isla Boca brava, Panamá. De un nido salieron polluelos y seis nidos fracasaron debido a la depredación. Yo documente cinco eventos de depredación de los cuales cuatro fueron por aves y uno por mamíferos. Crested Oropendolas (Psarocolius decumanus) depredo dos nidos y Roadside Hawk (Buteo magnirostris) y el Black-chested Jay (Cyanocorax affinis) depredaron uno cada uno. El depredador mamífero fue un marsupial común (Didelphis marsupialis). Todas las depredaciones de aves fueron diurnas y la del mamífero fue nocturna. Mis resultados sugieren que las aves neotropicales están sujetas a una diversa gama de depredadores de nidos y posiblemente la depredación por aves puede ser una causa importante del fracaso de las nidadas en mi lugar de estudio. [source] Predators at bird nests in a northern hardwood forest in New HampshireJOURNAL OF FIELD ORNITHOLOGY, Issue 3 2006David I. King ABSTRACT Nest predation is the primary cause of nest failure in most passerine birds, and increases in nest predation associated with anthropogenic habitat disturbance are invoked as explanations for population declines of some bird species. In most cases, however, the identity of the nest predators is not known with certainty. We monitored active bird nests with infrared time-lapse video cameras to determine which nest predators were responsible for depredating bird nests in northern New Hampshire. We monitored 64 nests of 11 bird species during three breeding seasons, and identified seven species of predators during 14 predation events. In addition, we recorded two instances of birds defending nests from predators and, in both cases, these nests were ultimately lost to predation. These results contrast with other studies in terms of the relatively high proportion of nests depredated by raptors and mice, as well as the absence of any predation by snakes. The diverse suite of predators in this and other studies is likely to confound our understanding of patterns of nest predation relative to fragmentation and habitat structure. SINOPSIS La depredación de nidos es la causa principal del fracaso de anidamiento de muchos paserinos. El incremento en depredación ha sido asociado a disturbio antropogénico de habitat y considerado como la causa de la disminución poblacional de muchas especies de aves. En la mayoría de los casos, no se sabe a ciencia cierta quién es el depredador. Monitoreamos nidos activos con cámaras infrarojas de video que tomaban la acción en lapsos para determinar que depredadores eran responsables de la pérdida de nidos en el norte de New Hampshire. A lo largo de tres temporadas reproductivas monitoreamos 64 nidos, pertenecientes a 11 especies, e identificamos siete depredadores en 14 actos de depredación. Además, pudimos grabar dos casos en donde los aves defendieron sus nidos, aunque los nidos eventualmente fueron depredados posteriormente. Estos resultados contrastan con otros estudios en términos de la alta proporción de depredación por parte de rapaces y ratoncitos, y en la ausencia de depredación por parte de culebras. La diversidad de depredadores en este y otros estudios ampliará los conocimiento sobre los patrones de depredación en nidos, y su relación con la fragmentación y la estructura del hábitat. [source] The role of Steller sea lions in a large population decline of harbor sealsMARINE MAMMAL SCIENCE, Issue 4 2010Elizabeth A. Mathews Abstract We provide the first direct evidence that Steller sea lions will prey on harbor seals. Direct observations of predation on marine mammals at sea are rare, but when observed rates of predation are extrapolated, predation mortality may be found to be significant. From 1992 to 2002, harbor seals in Glacier Bay declined steeply, from 6,200 to 2,500 (,65%). After documenting that Steller sea lions were preying on seals in Glacier Bay, we investigated increased predation by sea lions as a potential explanation for the large decline. In five independent data sets spanning 21,25 yr and including 14,308 d of observations, 13 predation events were recorded. We conducted a fine-scale analysis for an intensively studied haul-out (Spider Island) and a broader analysis of all of Glacier Bay. At Spider Island, estimated predation by sea lions increased and could account for the entirety of annual pup production in 5 of 8 yr since 1995. The predation rate, however, was not proportional to the number of predators. Predation by Steller sea lions is a new source of mortality that contributed to the seal declines; however, life history modeling indicates that it is unlikely that sea lion predation is the sole factor responsible for the large declines. [source] Restoring a keystone predator may endanger a prey species in a human-altered ecosystem: the return of the snow leopard to Sagarmatha National ParkANIMAL CONSERVATION, Issue 6 2009S. Lovari Abstract Twenty-five years ago, the snow leopard Uncia uncia, an endangered large cat, was eliminated from what is now Sagarmatha National Park (SNP). Heavy hunting pressure depleted that area of most medium,large mammals, before it became a park. After three decades of protection, the cessation of hunting and the recovery of wild ungulate populations, snow leopards have recently returned (four individuals). We have documented the effects of the return of the snow leopard on the population of its main wild prey, the Himalayan tahr Hemitragus jemlahicus, a ,near-threatened' caprin. Signs of snow leopard presence were recorded and scats were collected along a fixed trail (130 km) to assess the presence and food habits of the snow leopard in the Park, from 2004 to 2006. Himalayan tahr, the staple of the diet, had a relative occurrence of 48% in summer and 37% in autumn, compared with the next most frequent prey, musk deer Moschus chrysogaster (summer: 20%; autumn: 15%) and cattle (summer: 15%; autumn: 27%). In early summer, the birth rate of tahr (young-to-female ratio: 0.8,0.9) was high. The decrease of this ratio to 0.1,0.2 in autumn implied that summer predation concentrated on young tahr, eventually altering the population by removing the kid cohort. Small populations of wild Caprinae, for example the Himalayan tahr population in SNP, are sensitive to stochastic predation events and may be led to almost local extinction. If predation on livestock keeps growing, together with the decrease of Himalayan tahr, retaliatory killing of snow leopards by local people may be expected, and the snow leopard could again be at risk of local extinction. Restoration of biodiversity through the return of a large predator has to be monitored carefully, especially in areas affected by humans, where the lack of important environmental components, for example key prey species, may make the return of a predator a challenging event. [source] Linkage disequilibrium and natural selection for mimicry in the Batesian mimic Hypolimnas misippus (L.) (Lepidoptera: Nymphalidae) in the AfrotropicsBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 1 2010IAN J. GORDON On two occasions, on opposite sides of the African continent (Cape Coast, Ghana, and Dar es Salaam, Tanzania), high adult population densities in the polymorphic butterfly Hypolimnas misippus (a presumed mimic of Danaus chrysippus) were followed by linkage disequilibrium in combinations of fore- and hindwing colour patterns. On both occasions, disequilibrium was caused by significant changes in morph frequencies favouring rarer and more mimetic forms. Recaptures were too few for analysis at Dar, although the changes there took place within a single generation and must have been the result of differential survival. Recapture rate data and survival rate estimates at Cape Coast support the hypothesis that selective predation was responsible, as does the observation of synchronous linkage disequilibrium at Dar in the model D. chrysippus, indicating parasitic mimicry. There was clear selection for the perfection of mimicry for forewings at Dar and for hindwings at Cape Coast. Disequilibrium is also reported for two other sites, Legon (Ghana) and Boksburg (South Africa) and, in all four sites, it was associated with an increase in the most mimetic forms. New chemical evidence is presented to support the contention that D. chrysippus is a defended model. Although all the evidence leads to the conclusion that H. misippus is a Batesian mimic of D. chrysippus, many questions remain, particularly with regard to the identity of predators, the episodic nature of selective predation events, and their apparent lack of lasting and significant impact on overall gene frequencies. We conclude that H. misippus presents both challenges and opportunities for studies on mimicry, and we suggest that linkage disequilibrium can be a useful generic indicator for Gestalt predation on polymorphic prey. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 100, 180,194. [source] | |||||||||||||