Abstract:Tail autotomy, the self-induced tail separation from the body, is a common and effective antipredator mechanism in lizards. In this study, we examine the muscle energetics of tail shedding in six lacertid lizard species (Podarcis erhardii, Podarcis peloponnesiaca, Podarcis muralis, Podarcis gaigeae, Podarcis milensis, and Lacerta graeca) from the northeast Mediterranean region. Very long periods of postautotomy tail movement were demonstrated for all species ( min), and differences range p 6-8 among species we… Show more
“…According to our predictions, as a consequence of the higher autotomy rate and the more intense movement, individuals from Colom and Sargantana should accumulate higher lactate levels than those from Aire. Nevertheless, we failed to detect any difference among populations just as recorded in other lacertids species (Pafilis et al 2005). Anaerobic metabolism is a common energy production mechanism among reptiles (Pough and Andrews 1985).…”
Section: Discussioncontrasting
confidence: 63%
“…1) can be explained by the limited sample size in the case of predation simulation). Yet, the value for Aire (74%) is still high as compared to other lacertids (Pérez-Mellado et al 1997;Pafilis et al 2005). We believe that the reason must be attributed to the extremely dense population of the islet, estimated at around 4,100 individuals/ha (as opposed to 1,600 for Colom and 690 for Sargantana, Pérez-Mellado 1998).…”
Section: Discussionmentioning
confidence: 79%
“…Hence, it seems that the isolation time has been too short for a selective adaptation regarding postautotomic tail activity. This point is further indicated by the longer duration of tail thrashing of lacertids from eastern Mediterranean islands (Pafilis et al 2005) where predation pressure has been always heavy, as fossil records indicate (Kotsakis 1981;Caloi et al 1988). Postautotomy movement had to be more prolonged in eastern species so as to offset the severe predation strain.…”
Section: Discussionmentioning
confidence: 95%
“…Postautotomy movement is fueled by glycogen, which is oxidized anaerobically into lactate, providing the required energy to the muscles Fitzpatrick 1981, 1983;Gleeson 1996). Physiological pathways involved in tail muscle energetics have been reported as sharing a common pattern among species of the same family (Pafilis et al 2005). However, interspecies divergences in phylogeny may introduce biases that can easily obscure a real pattern or even create a spurious one (Huey 1987;Pianka 2001).…”
Caudal autotomy is an effective antipredator strategy widespread among lizards. The shed tail thrashes vigorously for long periods to distract the predator and facilitate the lizard's escape. This movement is maintained by energy supplied by the anaerobic conversion of glycogen into lactate. It has been suggested that lactate accumulation serves as an index for the vigor of tail thrashing. We made three predictions: (1) tail loss frequency should be higher under heavier predation regime, (2) the duration of postautotomy tail movement should be extended in populations under heavy predation pressure as an adaptation to the higher risk and the increased need for defense, and (3) as result, lactate in these tail tissues should be concentrated at higher levels. To eliminate the impact of phylogeny and environmental factors on the interpretation of our result, we focused exclusively on one species, the Balearic lizard (Podarcis lilfordi). We studied three populations under different predation pressure but sharing the same climatic conditions. We found no differences among the studied populations either in postautotomy duration of tail movement or in levels of final lactate accumulation while autotomy frequency was higher where predation pressure was more intense. Tail loss effectiveness is directly influenced by the level of predation, while secondary features of the trait appear to remain independent from the impact of environment.
“…According to our predictions, as a consequence of the higher autotomy rate and the more intense movement, individuals from Colom and Sargantana should accumulate higher lactate levels than those from Aire. Nevertheless, we failed to detect any difference among populations just as recorded in other lacertids species (Pafilis et al 2005). Anaerobic metabolism is a common energy production mechanism among reptiles (Pough and Andrews 1985).…”
Section: Discussioncontrasting
confidence: 63%
“…1) can be explained by the limited sample size in the case of predation simulation). Yet, the value for Aire (74%) is still high as compared to other lacertids (Pérez-Mellado et al 1997;Pafilis et al 2005). We believe that the reason must be attributed to the extremely dense population of the islet, estimated at around 4,100 individuals/ha (as opposed to 1,600 for Colom and 690 for Sargantana, Pérez-Mellado 1998).…”
Section: Discussionmentioning
confidence: 79%
“…Hence, it seems that the isolation time has been too short for a selective adaptation regarding postautotomic tail activity. This point is further indicated by the longer duration of tail thrashing of lacertids from eastern Mediterranean islands (Pafilis et al 2005) where predation pressure has been always heavy, as fossil records indicate (Kotsakis 1981;Caloi et al 1988). Postautotomy movement had to be more prolonged in eastern species so as to offset the severe predation strain.…”
Section: Discussionmentioning
confidence: 95%
“…Postautotomy movement is fueled by glycogen, which is oxidized anaerobically into lactate, providing the required energy to the muscles Fitzpatrick 1981, 1983;Gleeson 1996). Physiological pathways involved in tail muscle energetics have been reported as sharing a common pattern among species of the same family (Pafilis et al 2005). However, interspecies divergences in phylogeny may introduce biases that can easily obscure a real pattern or even create a spurious one (Huey 1987;Pianka 2001).…”
Caudal autotomy is an effective antipredator strategy widespread among lizards. The shed tail thrashes vigorously for long periods to distract the predator and facilitate the lizard's escape. This movement is maintained by energy supplied by the anaerobic conversion of glycogen into lactate. It has been suggested that lactate accumulation serves as an index for the vigor of tail thrashing. We made three predictions: (1) tail loss frequency should be higher under heavier predation regime, (2) the duration of postautotomy tail movement should be extended in populations under heavy predation pressure as an adaptation to the higher risk and the increased need for defense, and (3) as result, lactate in these tail tissues should be concentrated at higher levels. To eliminate the impact of phylogeny and environmental factors on the interpretation of our result, we focused exclusively on one species, the Balearic lizard (Podarcis lilfordi). We studied three populations under different predation pressure but sharing the same climatic conditions. We found no differences among the studied populations either in postautotomy duration of tail movement or in levels of final lactate accumulation while autotomy frequency was higher where predation pressure was more intense. Tail loss effectiveness is directly influenced by the level of predation, while secondary features of the trait appear to remain independent from the impact of environment.
“…Ease of caudal autotomy should also balance benefits and costs [14]. Because intact tails indicate social status and also play important roles in locomotion, courtship, defence and as lipid storage sites [15], the costs of caudal autotomy may outweigh the benefits under conditions of relaxed predation [16]. On small islands with few or no predators, the most expensive behaviours are predicted to be lost first [5].…”
Exotic predators have driven the extinction of many island species. We examined impacts of feral cats on the abundance and anti-predator behaviours of Aegean wall lizards in the Cyclades (Greece), where cats were introduced thousands of years ago. We compared populations with high and low cat density on Naxos Island and populations on surrounding islets with no cats. Cats reduced wall lizard populations by half. Lizards facing greater risk from cats stayed closer to refuges, were more likely to shed their tails in a standardized assay, and fled at greater distances when approached by either a person in the field or a mounted cat decoy in the laboratory. All populations showed phenotypic plasticity in flight initiation distance, suggesting that this feature is ancient and could have helped wall lizards survive the initial introduction of cats to the region. Lizards from islets sought shelter less frequently and often initially approached the cat decoy. These differences reflect changes since islet isolation and could render islet lizards strongly susceptible to cat predation.
Resource availability, competition, and predation commonly drive body size evolution. We assess the impact of high food availability and the consequent increased intraspecific competition, as expressed by tail injuries and cannibalism, on body size in Skyros wall lizards (Podarcis gaigeae). Lizard populations on islets surrounding Skyros (Aegean Sea) all have fewer predators and competitors than on Skyros but differ in the numbers of nesting seabirds. We predicted the following: (1) the presence of breeding seabirds (providing nutrients) will increase lizard population densities; (2) dense lizard populations will experience stronger intraspecific competition; and (3) such aggression, will be associated with larger average body size. We found a positive correlation between seabird and lizard densities. Cannibalism and tail injuries were considerably higher in dense populations. Increases in cannibalism and tail loss were associated with large body sizes. Adult cannibalism on juveniles may select for rapid growth, fuelled by high food abundance, setting thus the stage for the evolution of gigantism.
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