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Pressures Acting (pressure + acting)
Selected AbstractsTHE EVOLUTION OF WING COLOR: MALE MATE CHOICE OPPOSES ADAPTIVE WING COLOR DIVERGENCE IN COLIAS BUTTERFLIESEVOLUTION, Issue 5 2003Jacintha Ellers Abstract Correlated evolution of mate signals and mate preference may be constrained if selection pressures acting on mate preference differ from those acting on mate signals. In particular, opposing selection pressures may act on mate preference and signals when traits have sexual as well as nonsexual functions. In the butterfly Colias philodice eriphyle, divergent selection on wing color across an elevational gradient in response to the thermal environment has led to increasing wing melanization at higher elevations. Wing color is also a long-range signal used by males in mate searching. We conducted experiments to test whether sexual selection on wing melanization via male mate choice acts in the same direction as natural selection on mate signals due to the thermal environment. We performed controlled mate choice experiments in the field over an elevational range of 1500 meters using decoy butterflies with different melanization levels. Also, we obtained a more direct estimate of the relation between wing color and sexual selection by measuring mating success in wild-caught females. Both our experiments showed that wing melanization is an important determinant of female mating success in C. p. eriphyle. However, a lack of elevational variation in male mate preference prevents coevolution of mate signals and mate preference, as males at all elevations prefer less-melanized females. We suggest that this apparently maladaptive mate choice may be maintained by differences in detectability between the morphs or by preservation of species recognition. [source] THE EVOLUTION OF SEXUAL SIZE DIMORPHISM IN THE HOUSE FINCH.EVOLUTION, Issue 6 2000Abstract Recent colonization of ecologically distinct areas in North America by the house finch (Carpodacus mexicanus) was accompanied by strong population divergence in sexual size dimorphism. Here we examined whether this divergence was produced by population differences in local selection pressures acting on each sex. In a long-term study of recently established populations in Alabama, Michigan, and Montana, we examined three selection episodes for each sex: selection for pairing success, overwinter survival, and within-season fecundity. Populations varied in intensity of these selection episodes, the contribution of each episode to the net selection, and in the targets of selection. Direction and intensity of selection strongly differed between sexes, and different selection episodes often favored opposite changes in morphological traits. In each population, current net selection for sexual dimorphism was highly concordant with observed sexual dimorphism,in each population, selection for dimorphism was the strongest on the most dimorphic traits. Strong directional selection on sexually dimorphic traits, and similar intensities of selection in both sexes, suggest that in each of the recently established populations, both males and females are far from their local fitness optimum, and that sexual dimorphism has arisen from adaptive responses in both sexes. Population differences in patterns of selection on dimorphism, combined with both low levels of ontogenetic integration in heritable sexually dimorphic traits and sexual dimorphism in growth patterns, may account for the close correspondence between dimorphism in selection and observed dimorphism in morphology across house finch populations. [source] Three-dimensional analysis of single pile response to lateral soil movementsINTERNATIONAL JOURNAL FOR NUMERICAL AND ANALYTICAL METHODS IN GEOMECHANICS, Issue 8 2002J. L. Pan Abstract Three-dimensional finite element analysis was carried out to investigate the behaviour of single piles subjected to lateral soil movements and to determine the ultimate soil pressures acting along the pile shaft. The finite element analysis program ABAQUS was used for the analysis and run on a SUN Workstation. The von Mises constitutive model was employed to model the non-linear stress,strain soil behaviour. The pile was assumed to have linear elastic behaviour. This was considered to be a reasonable approximation, as the maximum stress developed in the pile did not exceed the yield stress of the concrete pile. The length of the pile is 15 m, the width of the square pile is 1 m. The three-dimensional finite element mesh used in the analysis was optimized taking into account the computing capacity limitations of the Sun Workstation. The computed ultimate soil pressures agreed well with those from the literature. The shapes of the soil pressure versus soil movement curves and the soil pressure versus the relative soil,pile displacement curves as well as the magnitude of the relative soil,pile displacement to mobilize the ultimate soil pressures were in reasonable agreement with those reported by other researchers. Copyright © 2002 John Wiley & Sons, Ltd. [source] How to use molecular marker data to measure evolutionary parameters in wild populationsMOLECULAR ECOLOGY, Issue 7 2005DANY GARANT Abstract Estimating the genetic basis of phenotypic traits and the selection pressures acting on them are central to our understanding of the evolution and conservation of wild populations. However, obtaining such evolutionary-related parameters is not an easy task as it requires accurate information on both relatedness among individuals and their breeding success. Polymorphic molecular markers are very useful in estimating relatedness between individuals and parentage analyses are now extensively used in most taxa. The next step in the application of molecular data to wild populations is to use them to derive estimates of evolutionary-related parameters for quantitative traits, such as quantitative genetic parameters (e.g. heritability, genetic correlations) and measures of selection (e.g. selection gradients). Despite their great appeal and potential, the optimal use of molecular tools is still debated and it remains unclear how they should best be used to obtain reliable estimates of evolutionary parameters in the wild. Here, we review the methods available for estimating quantitative genetic and selection parameters and discuss their merits and shortcomings, to provide a tool that summarizes the potential uses of molecular data to obtain such parameters in wild populations. [source] | ||||||||||