Although rapid adaptive changes in morphology on ecological time scales are now well documented in natural populations, the effects of such changes on whole-organism performance capacity and the consequences on ecological dynamics at the population level are often unclear. Here we show how lizards have rapidly evolved differences in head morphology, bite strength, and digestive tract structure after experimental introduction into a novel environment. Despite the short time scale (Ϸ36 years) since this introduction, these changes in morphology and performance parallel those typically documented among species and even families of lizards in both the type and extent of their specialization. Moreover, these changes have occurred side-by-side with dramatic changes in population density and social structure, providing a compelling example of how the invasion of a novel habitat can evolutionarily drive multiple aspects of the phenotype.bite force ͉ diet ͉ evolution ͉ gut structure
We investigated the possible role of variation in predation pressure in the phenotypic divergence of two island populations of the Italian wall lizard, Podarcis sicula . In 1971, ten adult specimens from the island of Pod Kopište (Adriatic Sea, Croatia) were transported to the island of Pod Mrčaru, 3.5 km east, where they founded a new population. Although the two islands resemble each other in general physiognomy (size, elevation, microclimate) and in the absence of terrestrial predators, lizards from the newly established population are now on average larger and have shorter hind limbs. They also exhibit lower maximal sprint speed as measured on a racetrack, and fatigue faster when chased in a torus track. In the field, lizards from the original population of Pod Kopište respond to a simulated predatory attack by fleeing at larger approach distances and by running further from the predator than lizards from Pod Mrčaru. These changes in morphology, behaviour and performance may result from the relaxed predation intensity on the latter island. Our analysis of the structural features of the microhabitats suggests that the vegetation on Pod Mrčaru offers more protection to lizards. Also, plasticine models of lizards, laid out on the islands, less often exhibited signs of being attacked by birds on Pod Mrčaru than on Pod Kopište. Our findings provide an example of how changes in (possibly a single) environmental factor may simultaneously produce responses in behaviour, morphology and whole-animal physiology, and this on a surprisingly small spatial and temporal scale.
Within populations, individual animals may vary considerably in morphology and ecology. The degree to which variation in morphology is related to ecological variation within a population remains largely unexplored. We investigated whether variation in body size and shape among sexes and age classes of the lizard Podarcis melisellensis translates in differential whole-animal performance (sprint speed, bite force), escape and prey attack behaviour in the field, microhabitat use and diet. Male and female adult lizards differed significantly in body size and head and limb proportions. These morphological differences were reflected in differences in bite strength, but not in sprint speed. Accordingly, field measurements of escape behaviour and prey attack speed did not differ between the sexes, but males ate larger, harder and faster prey than females. In addition to differences in body size, juveniles diverged from adults in relative limb and head dimensions. These shape differences may explain the relatively high sprint and bite capacities of juvenile lizards. Ontogenetic variation in morphology and performance is strongly reflected in the behaviour and ecology in the field, with juveniles differing from adults in aspects of their microhabitat use, escape behaviour and diet. . It is tempting to ascribe these ecological differences directly to sexual or ontogenetic differences in body size or shape, but theoretical developments in ecological morphology and empirical observations suggest that the relationship deserves closer inspection.In the spirit of Arnold's (1983) seminal contribution to ecological morphology, prudent assessments of the relationship between the morphology and the ecology of males and females, or juveniles and adults, requires measurements of whole-animal performance. These measurements will indicate whether the morphological variation observed is functionally and ecologically relevant, i.e. translates into differential performance. For instance, does sexual dimorphism in head size actually contribute to differences in bite performance? This is not self-evident, especially not when structures relevant in a survival context (e.g. aiding feeding or locomotion) are at the same time under sexual selection. Sexual selection for larger heads could, for example, theoretically increase head size in males without affecting muscle mass (Herrel Aguirre LF, Herrel A, Van Damme R, Mathyssen E. 2003. The implications of food hardness for diet in bats. Functional Ecology 17: 201-212. Arnold SJ. 1983. Morphology, performance and fitness. American Zoologist 23: 347-361. Bauwens D, Thoen C. 1981. Escape tactics and vulnerability to predation associated with reproduction in the lizard Lacerta vivipara. Journal of Animal Ecology 50: 733-743. Bonine KE, Garland T Jr. 1999. Sprint performance of phrynosomatid lizards, measured on a high-speed treadmill, correlates with hindlimb length. Journal of Zoology, London 248: 255-265. Bonnet X, Ineich I, Shine R. 2005. Terrestrial locomotion in sea snakes: the effects of sex and...
Summary1. Ecological interactions that involve aggressive confrontations between animals are important in shaping the evolution of morphology, behaviour and life history. However, as such confrontations are rarely witnessed, direct quantification of the intensity of these processes in natural populations is notoriously difficult. While the utilization of the frequency of non-lethal injuries is fraught with difficulties, it may provide information concerning different types of interaction, such as predation, intraspecific aggression and interspecific interference competition. 2. In this paper, we report on an exceptionally large difference in toe loss incidence between two populations of Podarcis sicula lizards living on small, neighbouring islands in the Adriatic Sea. We caught 900 lizards and recorded the number and location of missing toes. Subsequently, we investigated five non-mutually exclusive hypotheses concerning differences in bite force capacity, bone strength, predation intensity, average age and intraspecific aggression that may provide proximate explanations for the observed differences in injury frequencies. 3. Bite force differences differed considerably between the populations, but bone strength was found to be stronger in the populations with a higher frequency of natural scars. Predation pressure clearly differed between the populations, but we found higher injury rates under predation relaxation. 4. Our results indicate that density and consequently an increased intraspecific competition is the most likely explanation for the observed high frequencies of injuries. We suggest that the intensity of toe amputation between lizard populations may be a useable indirect indication for the intensity of intraspecific competition. 5. This study shows how a combination of morphological, physiological, behavioural and ecological measurements can be used to test assumptions implicit to alternative explanations of an observed phenomenon. Such tests can reveal how likely each of these explanations is, even if the processes leading to the phenomenon are difficult to observe directly.
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