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The relationship between genetic differentiation and phenotypic plasticity can provide information on whether plasticity generally facilitates or hinders adaptation to environmental change. Here, we studied wing shape variation in a damselfly (Lestes sponsa) across a latitudinal gradient in Europe that differed in time constraints mediated by photoperiod and temperature. We reared damselflies from northern and southern populations in the laboratory using a reciprocal transplant experiment that simulated time-constrained (i.e. northern) and unconstrained (southern) photoperiods and temperatures. After emergence, adult wing shape was analysed using geometric morphometrics. Wings from individuals in the northern and southern populations differed significantly in shape when animals were reared in their respective native environment. Comparing wing shape across environments, we found evidence for phenotypic plasticity in wing shape, and this response differed across populations (i.e. G x E interactions). This interaction was driven by a stronger plastic response by individuals from the northern population and differences in the direction of plastic wing shape changes among populations. The alignment between genetic and plastic responses depended on the specific combination of population and rearing environment. For example, there was an alignment between plasticity and genetic differentiation under time-constrained, but not under non-time-constrained conditions for forewings. We thus find mixed support for the hypothesis that environmental plasticity and genetic population differentiation are aligned. Furthermore, although our laboratory treatments mimicked the natural climatic conditions at northern and southern latitudes, the effects of population differences on wing shape were two to four times stronger than plastic effects. We discuss our results in terms of time constraints and the possibility that natural and sexual selection is acting differently on fore- and hind

Imperfect mimicry may be maintained when the various components of an aposematic signal have different salience for predators. Experimental laboratory studies provide robust evidence for this phenomenon. Yet, evidence from natural settings remains scarce. We studied how natural bird predators assess multiple features in a multicomponent aposematic signal in the Neotropical ‘clear wing complex’ mimicry ring, dominated by glasswing butterflies. We evaluated two components of the aposematic signal, wing colouration and wing morphology, in a predation experiment based on artificial replicas of glasswing butterflies (model) and Polythoridae damselflies (mimics) in their natural habitat. We also studied the extent of the colour aposematic signal in the local insect community. Finally, we inspected the nanostructures responsible for this convergent colour signal, expected to highly differ between these phylogenetically distinct species. Our results provide direct evidence for a stronger salience of wing colouration than wing morphology, as well as stronger selection on imperfect than in perfect colour mimics. Additionally, investigations of how birds perceive wing colouration of the local insect community provides further evidence that a UV‐reflective white colouration is being selected as the colour aposematic signal of the mimicry ring. Using electron microscopy, we also suggest that damselflies have convergently evolved the warning colouration through a pre‐adaptation. These findings provide a solid complement to previous experimental evidence suggesting a key influence of the cognitive assessment of predators driving the evolution of aposematic signals and mimicry rings.

Understanding why species range sizes vary is important for predicting the impact of environmental change on biodiversity. Here we use a multi-variable approach in a phylogenetic comparative context to understand how four morphological, two ecological, and two eco-geographical variables are associated with range size, latitudinal range and longitudinal range in 81 species of North-American libellulid dragonflies. Our results show that: 1) migratory species and species with a more expanded basal hindwing lobe have a larger range size; 2) opposite to Rapoport's rule, latitudinal range is negatively correlated with mid-range latitude; 3) longitudinal range is predicted by wing morphology and migration; 4) body size and larval habitat are not correlated with range size, latitudinal range or longitudinal range. These results suggest that dispersal-related traits, such as wing shape and migratory status, are important factors in predicting the range size of libellulid dragonflies. In addition, the reverse Rapoport's rule suggests that more northern-centred species might be more specialized than more southern-centred species. We suggest that the variables predicting range size are likely imposed by taxon-specific morphological, ecological, physiological and behavioural traits. Taxon-specific knowledge is thus necessary to understand the dynamics of range sizes and is important to implement successful restoration and conservation plans of threatened species.

Wing shape is related to flight performance, which is expected to be under selection for improving flight behaviours such as predator avoidance. Moreover, wing conspicuousness, usually involved in sexual selection processes, is also relevant in terms of predation risk. In this study, we examined how predation by a passerine bird, the white wagtail Motacilla alba, selects wing shape and wing colour patch size in males of the banded demoiselle Calopteryx splendens. The wing colour patch is intra- and intersexually selected in the study species. In a field study, we compared wings of live damselflies to wings of predated damselflies which are always discarded after predation. Based on aerodynamic theory and a previous study on wing shape of territorial tactics in damselflies, we predicted an overall short and broad wing, with a concave front margin shape to be selected by predation. This shape would be expected to improve escaping ability. Moreover, we predicted that wing patch size should be negatively selected by predation. We found that selection operated differently on fore- and hindwings. In contrast to our predictions, predation favoured a slender general forewing shape. However, the predicted wing shape was favoured in hindwings. We also found selection favouring a narrower wing colour patch. Our results suggest different roles of fore- and hindwings in flight, as previously suggested for Calopteryx damselflies and shown for butterflies and moths. Forewings would be more involved in sustained flight and hindwings in flight manoeuvrability. Our results differ somehow from a recently published work in the same study system, but using another population, suggesting that selection can fluctuate across space, despite the simplicity of this predator-prey system.

Ornaments may show hyperallometry in certain taxa, i.e. large individuals have proportionally larger ornaments than small ones. One hypothesis suggests that higher sexual selection intensity leads to steeper hyperallometric patterns. This study tested whether an ornamental trait subject to both intra- and intersexual selection showed steeper allometric slopes than when subject solely to intrasexual selection. The study employed the sexually selected male wing pigmentation of 14 calopterygid species (damselflies) that differ in sexual selection intensity (intrasexual selection versus intra- and intersexual selection). Hyperallometry was not a uniform pattern in the study species. Furthermore, the allometric slopes did not differ between sexual selection intensities. The allometry of ornamental traits is therefore highly variable even among related species. Other selection pressures-probably species-specific and at a local scale-acting on wing pigmentation might explain the diversity of allometric patterns.

Female-limited colour polymorphisms are widespread in Odonata, usually showing an androchrome and one or more gynochromes. Androchromes have been hypothesized to function as male mimics with a consequent decrease of male harassment, although males may also learn to recognize the different female colour morphs. In the Eurasian damselfly Lestes sponsa, the occurrence of two female colour morphs (androchrome and gynochrome) has been known since the beginning of the twentieth century, although this has been generally overlooked. In this work, we studied a Swedish population of L. sponsa by counting the number of females of each morph during nine consecutive days, as well as the number of tandems. Androchromes showed blue pruinescence at similar body parts as males, although more limited at the tip of the abdomen. Moreover, androchromes also showed bright blue coloured eyes as males. We found no indication that androchromes might be a result of age changes in female coloration. The androchrome morph accounted for 19% of the female population. Androchromes did not form tandems at a lower frequency than expected in the population, given the frequency of presence of each morph. Therefore our results suggest that either androchromes in this species do not function as male mimics, or that the population has reached equilibrium with equal fitness for each morph. Other aspects of male harassment and learned mate-recognition, as well as female morph behaviour, would shed light on the evolutionary and ecological significance of female morphs in this species.

Background: Wing size and shape have important aerodynamic implications on flight performance. We explored how wing size was related to wing shape in territorial males of 37 taxa of the damselfly family Calopterygidae. Wing coloration was also included in the analyses because it is sexually and naturally selected and has been shown to be related to wing shape. We studied wing shape using both the non-dimensional radius of the second moment of wing area (RSM) and geometric morphometrics. Lower values of the RSM result in less energetically demanding flight and wider ranges of flight speed. We also re-analyzed previously published data on other damselflies and dragonflies. Results: The RSM showed a hump-shaped relationship with wing size. However, after correcting for phylogeny using independent contrast, this pattern changed to a negative linear relationship. The basal genus of the study family, Hetaerina, was mainly driving that change. The obtained patterns were specific for the study family and differed from other damselflies and dragonflies. The relationship between the RSM and wing shape measured by geometric morphometrics was linear, but relatively small changes along the RSM axis can result in large changes in wing shape. Our results also showed that wing coloration may have some effect on RSM. Conclusions: We found that RSM showed a complex relationship with size in calopterygid damselflies, probably as a result of other selection pressures besides wing size per se. Wing coloration and specific behavior (e.g. courtship) are potential candidates for explaining the complexity. Univariate measures of wing shape such as RSM are more intuitive but lack the high resolution of other multivariate techniques such as geometric morphometrics. We suggest that the relationship between wing shape and size are taxa-specific and differ among closely-related insect groups.

Habitats are spatially and temporally variable, and organisms must be able to track these changes. One potential mechanism for this is dispersal by flight. Therefore, we would expect flying animals to show adaptations in wing shape related to habitat variation. In this work, we explored variation in wing shape in relation to preferred water body (flowing water or standing water with tolerance for temporary conditions) and landscape (forested to open) using 32 species of dragonflies of the genus Trithemis (80% of the known species). We included a potential source of variation linked to sexual selection: the extent of wing coloration on hindwings. We used geometric morphometric methods for studying wing shape. We also explored the phenotypic correlation of wing shape between the sexes. We found that wing shape showed a phylogenetic structure and therefore also ran phylogenetic independent contrasts. After correcting for the phylogenetic effects, we found (i) no significant effect of water body on wing shape; (ii) male forewings and female hindwings differed with regard to landscape, being progressively broader from forested to open habitats; (iii) hindwings showed a wider base in wings with more coloration, especially in males; and (iv) evidence for phenotypic correlation of wing shape between the sexes across species. Hence, our results suggest that natural and sexual selection are acting partially independently on fore- and hindwings and with differences between the sexes, despite evidence for phenotypic correlation of wing shape between males and females.

The static allometry between the size of a trait and the body size results from the net selection forces acting on the evolution of both the trait and the body size. An increased knowledge of the functional significance of traits is necessary to understand observed allometric patterns. We studied several traits of males of the beautiful demoiselle (Calopteryx virgo meridionalis Selys, 1873), for which there is a good functional knowledge of the genitalic traits and ornaments. We found positive allometry for the wing spot size (considered a secondary sexual trait) and for the distal width (but not length) of the anal appendages, which are used for grasping the female prior to copulation. Regarding the male secondary genitalia, the length but not the width of the big horns of the aedeagus showed an isometric pattern. The aedeagus shaft length showed a negative allometric pattern, while its distal width did not show a significant regression. The slopes of the regressions were higher when using wing length than when using body length as estimators of body size, with the exception of wing spot length. Results are discussed based on the functional significance of the study traits, as well as the pre- and post-copulatory selective pressures acting on them.

Body melanization may show adaptive variation related to thermoregulation ability, and it is to be expected that the degree of melanization will change among populations or closely related species across environmental gradients of solar radiation and/or environmental temperature. Some melanized secondary sexual traits may also play a role in sexual selection, leading to interpopulation variation, which would not be predicted by thermoregulation pressures alone. We studied the relationships between the interpopulation variation in wing pigmentation level (i.e. melanized secondary sexual trait) of two closely related species of Calopteryx damselfly, and both solar radiation and maximum environmental temperature estimates. Wing pigmentation differs between these species, is gender specific and is used in species' discrimination. Only Calopteryx virgo meridionalis males showed a significant negative partial correlation between wing pigmentation degree and temperature. However, C. virgo meridionalis females showed a positive significant partial correlation between wing pigmentation degree and solar radiation. Wing pigmentation in Calopteryx xanthostoma males was not related to solar radiation or temperature. Thus, thermoregulation pressures poorly explained the observed variations in wing pigmentation between populations, although they might have an adaptive significance at the species' level. As wing pigmentation showed important latitudinal variation, several other selection pressures which might act on melanized traits are briefly discussed. (C) 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 103, 36-44., Times Cited: 0

Under natural selection, wing shape is expected to evolve to optimize flight performance. However, other selective factors besides flight performance may influence wing shape. One such factor could be sexual selection in wing sexual ornaments, which may lead to alternative variations in wing shape that are not necessarily related to flight performance. In the present study, we investigated wing shape variations in a calopterygid damselfly along a latitudinal gradient using geometric morphometrics. Both sexes show wing pigmentation, which is a known signal trait at intra- and interspecific levels. Wing shape differed between sexes and, within the same sex, the shape of the hind wing differed from the front wing. Latitude and body size explained a high percentage of the variation in wing shape for female front and hind wings, and male front wings. In male hind wings, wing pigmentation explained a high amount of the variation in wing shape. On the other hand, the variation in shape explained by pigmentation was very low in females. We suggest that the conservative morphology of front wings is maintained by natural selection operating on flight performance, whereas the sex-specific differences in hind wings most likely could be explained by sexual selection. The observed sexual dimorphism in wing shape is likely a result of different sex-specific behaviours. (C) 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 102, 263-274., Times Cited: 1

Using bioclimatic belts as habitat and distribution predictors, the present study examines the implications of the potential distributions of the three Iberian damselflies, Calopteryx Leach (Odonata: Calopterygidae), with the aim of investigating the possible consequences in specific interactions among the species from a sexual selection perspective and of discussing biogeographical patterns. To obtain the known distributions, the literature on this genus was reviewed, relating the resulting distributions to bioclimatic belts. Specific patterns related to bioclimatic belts were clearly observed in the Mediterranean region. The potential distribution maps and relative frequencies might involve latitudinal differences in relative abundances, C. virgo meridionalis Selys being the most abundant species in the Eurosiberian region, C. xanthostoma (Charpentier) in the northern half of the Mediterranean region and C. haemorrhoidalis (Vander Linden) in the rest of this region. These differences might explain some previously described latitudinal differences in secondary sexual traits in the three species. Changes in relative abundances may modulate interactions among these species in terms of sexual selection and may produce sexual character displacement in this genus. C. virgo meridionalis distribution and ecological requirements explain its paleobiogeography as a species which took refuge in Iberia during the Wurm glaciation. Finally, possible consequences in species distributions and interactions are discussed within a global climate change context., Times Cited: 1