1989
DOI: 10.1016/s0003-3472(89)80142-3
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Behavioural responses to predators and predation risk in four species of larval anurans

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Cited by 259 publications
(215 citation statements)
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“…Our results imply that the response to the growth-mortality tradeoff differs between B. bombina and B. ariegata tadpoles as predicted by the ecology of their usual breeding habitats ; the genetically-determined behavioural patterns demonstrated here will serve to increase B. bombina's fitness relative to B. ariegata in a semipermanent pond. Differences in tadpole behaviour and susceptibility to predation have been found in other taxa and, similarly, have been invoked to explain species' distributions along environmental gradients or occupation of alternative ecological niches (Morin 1983 ;Woodward 1983 ;Lawler 1989 ;Chovanec 1992 ;Werner & McPeek 1994 ;Skelly 1995). The data are consistent with the hypothesis that predator-rich environments should contain less active species.…”
Section: Discussionsupporting
confidence: 79%
“…Our results imply that the response to the growth-mortality tradeoff differs between B. bombina and B. ariegata tadpoles as predicted by the ecology of their usual breeding habitats ; the genetically-determined behavioural patterns demonstrated here will serve to increase B. bombina's fitness relative to B. ariegata in a semipermanent pond. Differences in tadpole behaviour and susceptibility to predation have been found in other taxa and, similarly, have been invoked to explain species' distributions along environmental gradients or occupation of alternative ecological niches (Morin 1983 ;Woodward 1983 ;Lawler 1989 ;Chovanec 1992 ;Werner & McPeek 1994 ;Skelly 1995). The data are consistent with the hypothesis that predator-rich environments should contain less active species.…”
Section: Discussionsupporting
confidence: 79%
“…One possibility is that tadpoles that do not move will be less likely to be detected and eaten by predators. Odonate nymphs are important predators of many larval anuran species (Lawler, 1989;Skelly and Werner, 1990;Chovanec, 1992) and have been observed in the same ponds as Xenopus tadpoles in South Africa (Alan Roberts, personal observation). We therefore used damselfly nymphs (Zygoptera) to compare the predation of control tadpoles to those with denervated cement glands.…”
Section: Does Predation Increase When the Cement Gland Is Denervated?mentioning
confidence: 99%
“…At this stage of development (stage 37/38) there is no fitness cost in keeping still as the tadpoles have no mouth and do not start to feed until about 2 days later (Nieuwkoop and Faber, 1956). This contrasts with older tadpoles that need to move in order to feed but then face increased risk of predation, for example by dragonfly nymphs (Lawler, 1989;Chovanec, 1992). Such investigations on other tadpoles suggested that tonic inhibition during attachment in the hatchling Xenopus tadpole could be significant in reducing activity and as a consequence, reducing predation.…”
Section: Significance Of Tonic Inhibition During Attachmentmentioning
confidence: 99%
“…Previous studies of the hydroperiod gradient have focused on life history responses to drying and behavioral traits that potentially influence development and growth. Rates of development and sometimes growth are facultatively higher in drying ponds (Wilbur 1987, Merila¨et al 2000, and species differences in foraging activity can be correlated with pond permanence (Woodward 1983, Lawler 1989, Van Buskirk 2002, Richter-Boix et al 2007). However, causal relationships between external shape and developmental rate are unknown and perhaps unlikely, so the observed patterns of morphological change along the permanence gradient may have an explanation that does not directly involve pond drying.…”
Section: Relationships Between Morphology and Habitat Gradientsmentioning
confidence: 99%