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Escape Behaviours (escape + behaviour)
Selected AbstractsEscape behaviour and ultimate causes of specific induced defences in an anuran tadpoleJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 1 2005C. Teplitsky Abstract Induced defences, such as the predator avoidance morphologies in amphibians, result from spatial or temporal variability in predation risk. One important component of this variability should be the difference in hunting strategies between predators. However, little is known about how specific and effective induced defences are to different types of predators. We analysed the impact of both pursuing (fish, Gasterosteus aculeatus) and sit-and-wait (dragonfly, Aeshna cyanea) predators on tadpole (Rana dalmatina) morphology and performance (viz locomotive performance and growth rate). We also investigated the potential benefits of the predator-induced phenotype in the presence of fish predators. Both predators induced deeper tail fins in tadpoles exposed to threat of predation, and stickleback presence also induced longer tails and deeper tail muscles. Morphological and behavioural differences resulted in better escape ability of stickleback-induced tadpoles, leading to improved survival in the face of stickleback predation. These results clearly indicate that specific morphological responses to different types of predators have evolved in R. dalmatina. The specific morphologies suggest low correlations between the traits involved in the defence. Independence of traits allows prey species to fine-tune their response according to current predation risk, so that the benefit of the defence can be maximal. [source] Costs of Refuge Use Affect Escape Decisions of Iberian Rock Lizards Lacerta monticolaETHOLOGY, Issue 6 2000José Martín Theoretical models of anti-predator escape behaviour suggest that prey may adjust their escape response such that the optimal flight distance is the point at which the costs of staying exceed the costs of fleeing. Anti-predatory decisions should be made based also on consequences for long-term expected fitness, such as the costs of refuge use. For example, in lizards, the maintenance of an optimal body temperature is essential to maximize physiological processes. However, if unfavourable thermal conditions of refuges can decrease the body temperature of lizards, their escape decision should be influenced by refuge conditions. Analyses of the variation in flight distances and emergence latency from a refuge for the lizard Lacerta monticola under two different predation risk levels, and their relationship with the thermal environment, supported these predictions. When risk increased, lizards had longer emergence latencies, and thus costs of refuge use increased (a greater loss of time and body temperature). In the low-risk situation, lizards that were farther from the refuge had longer flight distances, whereas thermal conditions were less important. When risk increased, lizards had longer flight distances when refuges were farther off, but also when the external heating rate and the refuge cooling rate were lower. The results suggest that, in addition to the risk of predation, expected long-term fitness costs of refuges can also affect escape decisions. [source] Ontogeny of escape swimming performance in the spotted salamanderFUNCTIONAL ECOLOGY, Issue 3 2010Tobias Landberg Summary 1.,The life stage suffering the highest predation rate is expected to have the highest escape performance unless developmental or functional constraints interfere. Peak aquatic escape performance in ephemeral pond-breeding amphibians is expected to develop early in the larval period, and metamorphosis is expected to reduce or completely disrupt aquatic escape performance. In anurans, exceptionally low escape performance during metamorphosis creates selection favouring rapid metamorphosis , which minimizes the time individuals spend in the vulnerable transition between tadpole and frog. 2.,We investigated the development of aquatic escape performance in the spotted salamander, Ambystoma maculatum (Shaw, 1802), from embryonic development through metamorphosis. We expected performance to peak early in the larval period as hatchlings face high rates of predation but embryos must first develop escape behaviours. We also tested whether escape performance during metamorphosis was intermediate, as predicted by tail fin resorption, or lower than larvae and adults indicating a major physiological disruption. 3.,Escape performance shows a complex ontogeny that is first positively influenced by embryonic and early larval development and then negatively correlated with tail resorption and body size. Escape distance was the only performance metric not affected by life stage. In contrast, both escape velocity and duration showed ontogenetic peaks early in the larval period with the lowest performance found in early embryos and adults and intermediate performance during metamorphosis. 4.,This pattern suggests that metamorphosis does not impose a major physiological disruption on escape performance. Because spotted salamanders do not pass through a frog-like ,ontogenetic performance valley' during metamorphosis, they may be less subject than anurans to selection favouring rapid metamorphosis. 5.,Functional implications of phenotypic variation should be considered in an ontogenetic framework because the relationship between body size and escape performance can be reversed on either side of an ontogenetic performance peak. The assumption that metamorphosis radically disrupts basic functions such as predator evasion does not seem universally warranted and suggests examination of ontogenetic performance trajectories in a diversity of animals with complex life cycles. [source] Cephalopod chromatophores: neurobiology and natural historyBIOLOGICAL REVIEWS, Issue 4 2001J. B. MESSENGER ABSTRACT The chromatophores of cephalopods differ fundamentally from those of other animals: they are neuromuscular organs rather than cells and are not controlled hormonally. They constitute a unique motor system that operates upon the environment without applying any force to it. Each chromatophore organ comprises an elastic sacculus containing pigment, to which is attached a set of obliquely striated radial muscles, each with its nerves and glia. When excited the muscles contract, expanding the chromatophore; when they relax, energy stored in the elastic sacculus retracts it. The physiology and pharmacology of the chromatophore nerves and muscles of loliginid squids are discussed in detail. Attention is drawn to the multiple innervation of dorsal mantle chromatophores, of crucial importance in pattern generation. The size and density of the chromatophores varies according to habit and lifestyle. Differently coloured chromatophores are distributed precisely with respect to each other, and to reflecting structures beneath them. Some of the rules for establishing this exact arrangement have been elucidated by ontogenetic studies. The chromatophores are not innervated uniformly: specific nerve fibres innervate groups of chromatophores within the fixed, morphological array, producing ,physiological units' expressed as visible ,chromatomotor fields'. The chromatophores are controlled by a set of lobes in the brain organized hierarchically. At the highest level, the optic lobes, acting largely on visual information, select specific motor programmes (i.e. body patterns); at the lowest level, motoneurons in the chromatophore lobes execute the programmes, their activity or inactivity producing the patterning seen in the skin. In Octopus vulgaris there are over half a million neurons in the chromatophore lobes, and receptors for all the classical neurotransmitters are present, different transmitters being used to activate (or inhibit) the different colour classes of chromatophore motoneurons. A detailed understanding of the way in which the brain controls body patterning still eludes us: the entire system apparently operates without feedback, visual or proprioceptive. The gross appearance of a cephalopod is termed its body pattern. This comprises a number of components, made up of several units, which in turn contains many elements: the chromatophores themselves and also reflecting cells and skin muscles. Neural control of the chromatophores enables a cephalopod to change its appearance almost instantaneously, a key feature in some escape behaviours and during agonistic signalling. Equally important, it also enables them to generate the discrete patterns so essential for camouflage or for signalling. The primary function of the chromatophores is camouflage. They are used to match the brightness of the background and to produce components that help the animal achieve general resemblance to the substrate or break up the body's outline. Because the chromatophores are neurally controlled an individual can, at any moment, select and exhibit one particular body pattern out of many. Such rapid neural polymorphism (,polyphenism') may hinder search-image formation by predators. Another function of the chromatophores is communication. Intraspecific signalling is well documented in several inshore species, and interspecific signalling, using ancient, highly conserved patterns, is also widespread. Neurally controlled chromatophores lend themselves supremely well to communication, allowing rapid, finely graded and bilateral signalling. [source] | ||||||||||