Health status and immunocompetence have been proposed as important factors affecting individual variation in the attainment of breeding condition in birds. We studied individual variation in serological variables indicating health status (blood sedimentation rate, haematocrit, `buffy coat' layer, proportions of different types of leucocytes) in two groups of breeding chinstrap penguins Pygoscelis antarctica with breeding dates 9 days apart. We sampled these individuals shortly after hatching of their young and at the end of the chick-raising period. A group of failed breeders was also sampled. Birds of both sexes were included. We also measured the T-cell-mediated immune response as indicated by an in vivo hypersensitivity response to an intradermal injection of a mitogen (phytohaemagglutinin) in early and late breeders. Sex had no significant effect on most variables. Late breeders had poorer health (more leucocytes, especially heterophils and lymphocytes) and a lower T-cell-mediated immune response than early breeders. Failed breeders were more similar to late than to early breeders. Early breeders suffered a decline in health status throughout the chick-raising period. The impact of pathogens on variation in life history traits in avian populations may be important even in extreme Antarctic environments.
JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact support@jstor.org.. Ecological Society of America is collaborating with JSTOR to digitize, preserve and extend access to Ecology. Abstract.The foraging behavior of four Parus species feeding at artificial feeders was studied, while controlling for ecological variables related to patch characteristics (food quality, food access, and escape distance to the nearest refuge). Hindlimb morphology (osteology and myology) was analyzed and compared with foraging postures at feeders. Using the Long-Tailed Tit as an appropriate outgroup for comparison, and considering functional changes associated with morphological changes, we demonstrated the existence of clear ecomorphological patterns relating foraging postures and hindlimb morphology in the four Parus species studied. The Blue Tit uses hanging postures preferably and its hindlimb morphology is modified for helping leg flexion. The Crested Tit more often stands and its hindlimb morphology is modified to aid leg extension. Great and Coal Tits are ecologically and morphologically intermediate between the two former species. Our results show morphology as a determinant of locomotion mode. Since foraging postures are tightly associated with substrate use, then morphology should be considered when studying pressures determining community organization. Our proposed integrative method for dealing with ecomorphology can be valuable in demonstrating the adaptiveness of morphological structures in phylogenetically and ecologically related species.
BackgroundAnimals have been hypothesized to benefit from pendulum mechanics during suspensory locomotion, in which the potential energy of gravity is converted into kinetic energy according to the energy-conservation principle. However, no convincing evidence has been found so far. Demonstrating that morphological evolution follows pendulum mechanics is important from a biomechanical point of view because during suspensory locomotion some morphological traits could be decoupled from gravity, thus allowing independent adaptive morphological evolution of these two traits when compared to animals that move standing on their legs; i.e., as inverted pendulums. If the evolution of body shape matches simple pendulum mechanics, animals that move suspending their bodies should evolve relatively longer legs which must confer high moving capabilities.Methodology/Principal FindingsWe tested this hypothesis in spiders, a group of diverse terrestrial generalist predators in which suspensory locomotion has been lost and gained a few times independently during their evolutionary history. In spiders that hang upside-down from their webs, their legs have evolved disproportionately longer relative to their body sizes when compared to spiders that move standing on their legs. In addition, we show how disproportionately longer legs allow spiders to run faster during suspensory locomotion and how these same spiders run at a slower speed on the ground (i.e., as inverted pendulums). Finally, when suspensory spiders are induced to run on the ground, there is a clear trend in which larger suspensory spiders tend to run much more slowly than similar-size spiders that normally move as inverted pendulums (i.e., wandering spiders).Conclusions/SignificanceSeveral lines of evidence support the hypothesis that spiders have evolved according to the predictions of pendulum mechanics. These findings have potentially important ecological and evolutionary implications since they could partially explain the occurrence of foraging plasticity and dispersal constraints as well as the evolution of sexual size dimorphism and sociality.
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