Carry‐over effects of conditions at the wintering grounds on breeding plumage signals in a migratory bird: roles of phenotypic plasticity and selection

To understand the consequences of ever‐changing environment on the dynamics of phenotypic traits, distinguishing between selection processes and individual plasticity is crucial. We examined individual consistency/plasticity in several male secondary sexual traits expressed during the breeding season (white wing and forehead patch size, UV reflectance of white wing patch and dorsal melanin coloration) in a migratory pied flycatcher (Ficedula hypoleuca) population over an 11‐year period. Furthermore, we studied carry‐over effects of three environmental variables (NAO, a climatic index; NDVI, a vegetation index; and rainfall) at the wintering grounds (during prebreeding moult) on the expression of these breeding plumage traits of pied flycatcher males at individual and population levels. Whereas NAO correlates negatively with moisture in West Africa, NDVI correlates positively with primary production. Forehead patch size and melanin coloration were highly consistent within individuals among years, whereas the consistency of the other two traits was moderate. Wing patch size decreased with higher NAO and increased with higher rainfall and NDVI at the individual level. Interestingly, small‐patched males suffered lower survival during high NAO winters than large‐patched males, and vice versa during low NAO winters. These counteracting processes meant that the individual‐level change was masked at the population level where no relationship was found. Our results provide a good example of how variation in the phenotypic composition of a natural population can be a result of both environment‐dependent individual plasticity and short‐term microevolution. Moreover, when plasticity and viability selection operate simultaneously, their impacts on population composition may not be evident.     

RAPID LOSS OF BEHAVIORAL PLASTICITY AND IMMUNOCOMPETENCE UNDER INTENSE SEXUAL SELECTION

Phenotypic plasticity allows animals to maximize fitness by conditionally expressing the phenotype best adapted to their environment. Although evidence for such adjustment in reproductive tactics is common, little is known about how phenotypic plasticity evolves in response to sexual selection. We examined the effect of sexual selection intensity on phenotypic plasticity in mating behavior using the beetle Callosobruchus maculatus. Male genital spines harm females during mating and females exhibit copulatory kicking, an apparent resistance trait aimed to dislodge mating males. After exposing individuals from male‐ and female‐biased experimental evolution lines to male‐ and female‐biased sociosexual environments, we examined behavioral plasticity in matings with standard partners. While females from female‐biased lines kicked sooner after exposure to male‐biased sociosexual contexts, in male‐biased lines this plasticity was lost. Ejaculate size did not diverge in response to selection history, but males from both treatments exhibited plasticity consistent with sperm competition intensity models, reducing size as the number of competitors increased. Analysis of immunocompetence revealed reduced immunity in both sexes in male‐biased lines, pointing to increased reproductive costs under high sexual selection. These results highlight how male and female reproductive strategies are shaped by interactions between phenotypically plastic and genetic mechanisms of sexual trait expression.     

Climatic and temporal effects on the expression of secondary sexual characters: genetic and environmental components

Despite great interest in sexual selection, relatively little is known in detail about the genetic and environmental determinants of secondary sexual characters in natural populations. Such information is important for determining the way in which populations may respond to sexual selection. We report analyses of genetic and large-scale environmental components of phenotypic variation of two secondary sexual plumage characters (forehead and wing patch size) in the collared flycatcher Ficedula albicollis over a 22-year period. We found significant heritability for both characters but little genetic covariance between the two. We found a positive association between forehead patch size and a large-scale climatic index, the North Atlantic Oscillation (NAO) index, but not for wing patch. This pattern was observed in both cross-sectional and longitudinal data suggesting that the population response to NAO index can be explained as the result of phenotypic plasticity. Heritability of forehead patch size for old males, calculated under favorable conditions (NAO index > or = median), was greater than that under unfavorable conditions (NAO index < median). These changes occurred because there were opposing changes in additive genetic variance (VA) and residual variance (VR) under favorable and unfavorable conditions, with VA increasing and VR decreasing in good environments. However, no such effect was detected for young birds, or for wing patch size in either age class. In addition to these environmental effects on both phenotypic and genetic variances, we found evidence for a significant decrease of forehead patch size over time in older birds. This change appears to be caused by a change in the sign of viability selection on forehead patch size, which is associated with a decline in the breeding value of multiple breeders. Our data thus reveal complex patterns of environmental influence on the expression of secondary sexual characters, which may have important implications for understanding selection and evolution of these characters.     

Sensitive periods during the development and expression of vertebrate sexual signals: A systematic review

Many sexually selected traits exhibit phenotypic plasticity. Despite a growing appreciation for the ecological context in which sexual selection occurs, and for the role of plasticity in shaping traits associated with local adaptation and divergence, there is an important gap in knowledge about the onset and duration of plasticity in sexual trait expression. Integrating this temporal dimension of plasticity into models of sexual selection informs our understanding of the information conveyed by sexual traits and our predictions related to trait evolution, and is critical in this time of unprecedented and rapid environmental change. We conducted a systematic review of 869 studies to ask how trait modalities (e.g., visual and chemical) relate to the onset and duration of plasticity in vertebrate sexual signals. We show that this literature is dominated by studies of coloration in birds and fish, and most studies take place during the breeding season. Where possible, we integrate results across studies to link physiology of specific trait modalities with the life stage (e.g., juvenile, breeding, or nonbreeding) during which plasticity occurs in well‐studied traits. Limitations of our review included a lack of replication in our dataset, which precluded formal analysis. We argue that the timing of trait plasticity, in addition to environmental context, is critical for determining whether and how various communication signals are associated with ecological context, because plasticity may be ongoing or occur at only one point in an individual''s lifetime, and determining a fixed trajectory of trait expression. We advocate for careful consideration of the onset and duration of plasticity when analyzing how environmental variation affects sexual trait expression and associated evolutionary outcomes.     

A partly coverable badge signalling avian virus resistance

We investigated whether the sexually selected forehead patch of the collared flycatcher Ficedula albicollis is an honest badge of status indicating quality expressed as immunological response. We used both manual measurements and digital measurements, the latter based on photographs. Badge‐size data were collected during the mating period and during the nestling feeding period to capture trait plasticity. Concomitant with first sample collection, birds were inoculated with a novel antigen. Antibody response was strongly and positively correlated with badge expression during the mating period and with the increase in badge expression during the mating period as compared with outside this period. The results support the Hansen and Rohwer theory of coverable badges, are consistent with the immunocompetence handicap hypothesis and with the good genes model suggesting that, on a population level, the expression of secondary sexual traits should be an honest signal positively associated with traits that are beneficial for survival. The results also suggest that manual measurements of this type of secondary sexual trait are sufficiently exact.     

Fluctuations in population composition dampen the impact of phenotypic plasticity on trait dynamics in superb fairy-wrens

1. In structured populations, phenotypic change can result from changes throughout an individual's lifetime (phenotypic plasticity, age-related changes), selection and changes in population composition (environment- or density-driven fluctuations in age-structure). 2. The contribution of population dynamics to phenotypic change has often been ignored. However, for understanding trait dynamics, it is important to identify both the individual- and population-level mechanisms responsible for trait change, because they potentially reinforce or counteract each other. 3. We use 22 years of field data to investigate the dynamics of a sexually selected phenological trait, the timing of nuptial moult in superb fairy-wrens Malurus cyaneus. 4. We show that trait expression is both climate- and age-dependent, but that phenotypic plasticity in response to climate variability also varies with age. Old males can acquire nuptial plumage very early after high rainfall, but 1- to 2-year-olds cannot. However, males of all ages that defer moult to later in the year acquire nuptial plumage earlier when conditions are warmer. 5. The underlying mechanism appears to be that old males may risk moulting in the most challenging period of the year: in autumn, when drought restricts food abundance and during the cold winter. By contrast, young males always moult during the spring transition to benign - warmer and generally wetter - conditions. Temperature changes dominate this transition that heralds the breeding season, thereby causing both young and late-moulting older birds to be temperature sensitive. 6. Climate and age also affect trait dynamics via a population dynamical pathway. The same high rainfall that triggers early moulting in old males concurrently increases offspring recruitment and thereby reduces the average age of males in the population. Consequently, effects of rainfall on trait dynamics through phenotypic plasticity of old males are dampened by synchronous rejuvenation of the age-structure. 7. A long-term trend towards drier environments prompted phenotypic change because of plasticity, but this was masked by climate-driven demographic change (causing apparent stasis). This suggests a novel explanation for why trait change may fail to reflect the observed pattern of directional selection or phenotypic plasticity.     

Depigmented wing patch size is a condition-dependent indicator of viability in male collared flycatchers

Honesty of sexual advertisement is thought to be the resultof signalling costs. Because production costs of depigmentedplumage patches are probably very low, their role as honestsignals of individual quality has been questioned. Costs ofbearing these traits, however, should also be taken into account.Studies on proximate determination and possible informationcontent of white badges are very rare. We investigated repeatability,sensu lato heritability, and condition- and age-dependence ofwhite wing patch size, a male display trait in a populationof collared flycatchers (Ficedula albicollis), based on 4 yearsof data. By comparing relationships between age and wing patchsize (1) within individuals among years versus (2) among individualswithin years, we could address the viability indicator valueof the trait. Wing patch size approximately doubled at the transitionfrom subadult to adult plumage, and its change was significantlyrelated to body condition the previous season. Repeatabilityand heritability values suggest that the trait is informativealready in subadult plumage, and that genetic and early environmentaleffects are important in its determination, the latter onlyduring the first year of life. Thus, wing patch size can actas a condition-dependent signal of genetic quality. Indeed,discrepancy between results from the horizontal and verticalage-dependence approaches shows that the trait was positivelyrelated to expected lifespan. After examining several alternativeexplanations, we conclude that wing patch size indicates geneticallybased viability. This is the first study to demonstrate a goodgenes viability benefit conferred by a depigmented plumage patch.     

By-product runaway evolution by adaptive mate choice: A behavioural aspect of sexual selection

Summary From a behavioural perspective on adaptive female choice, I developed a by-product runaway model of adaptive mate choice. The model illustrates the evolution of the tail size of peacocks. I consider the causal mechanisms of adaptive female choice: (1) why (ultimate reasons); (2) how (proximate mechanisms). Assumptions are developed based on these behavioural aspects. For (1) ultimate reasons, I assume that many male losers (low-fitness males) always occur due to genetic and environmental uncertainty (A-1). For (2) proximate mechanisms, I assume that losers tend to differ in the expression of a fitness-sensitive trait (an ultimate target, e.g. body size; A-2), that the fitness-sensitive trait correlates with a secondary sexual trait (a proximate cue, e.g. allometry in body size and tail size; (A-3), and that the cue trait has a genetic basis that is independent of the target trait (e.g. a genetic basis in tail ratio to body size; A-4). The model's results are: persistent female choice by means of a proximate cue (R-1); by-product selection on the independent genetic basis of the cue (R-2); and the non-adaptive or maladaptive runaway evolution of the male proximate cue (R-3). In this model, female mate preferences are non-arbitrary and adaptive, whereas the resulting evolution of male secondary sexual traits is non-adaptive in the sense of survival selection.     

Maternal effects on phenotypic plasticity in larvae of the salamander <Emphasis Type="Italic">Hynobius retardatus</Emphasis>

Maternal effects are widespread and influence a variety of traits, for example, life history strategies, mate choice, and capacity to avoid predation. Therefore, maternal effects may also influence phenotypic plasticity of offspring, but few studies have addressed the relationship between maternal effects and phenotypic plasticity of offspring. We examined the relationship between a maternally influenced trait (egg size) and the phenotypic plasticity of the induction rate of the broad-headed morph in the salamander Hynobius retardatus. The relationship between egg size and the induction of the broad-headed morph was tested across experimental crowding conditions (densities of low conspecifics, high conspecifics, and high heterospecific anuran), using eggs and larvae from eight natural populations with different larval densities of conspecifics and heterospecifics. The broad-headed morph has a large mouth that enables it to consume either conspecifics or heterospecifics, and this ability gives survival advantages over the normal morph. We have determined that there is phenotypic plasticity in development, as shown by an increase in the frequency of broad-headed morph in response to an increase in the density of conspecifics and heterospecifics. This reaction norm differed between populations. We also determined that the frequency of the broad-headed morph is affected by egg size in which larger egg size resulted in expression of the broad-headed morph. Furthermore, we determined that selection acting on the propensity to develop the broad-headed morph has produced a change in egg size. Lastly, we found that an increase in egg size alters the reaction norm to favor development of the broad-headed morph. For example, an equal change in experimental density produces a greater change in the frequency of the broad-headed morph in larvae developing from large eggs than it does in larvae developing from small eggs. Population differences in plasticity might be the results of differences in egg size between populations, which is caused by the adaptive integration of the plasticity and egg size. Phenotypic plasticity can not evolve independently of maternal effects.     

Sexual selection explains sex-specific growth plasticity and positive allometry for sexual size dimorphism in a reef fish

In 1950, Rensch noted that in clades where males are the larger sex, sexual size dimorphism (SSD) tends to be more pronounced in larger species. This fundamental allometric relationship is now known as ‘Rensch''s rule’. While most researchers attribute Rensch''s rule to sexual selection for male size, experimental evidence is lacking. Here, we suggest that ultimate hypotheses for Rensch''s rule should also apply to groups of individuals and that individual trait plasticity can be used to test those hypotheses experimentally. Specifically, we show that in the sex-changing fish Parapercis cylindrica, larger males have larger harems with larger females, and that SSD increases with harem size. Thus, sexual selection for male body size is the ultimate cause of sexual size allometry. In addition, we experimentally illustrate a positive relationship between polygyny potential and individual growth rate during sex change from female to male. Thus, sexual selection is the ultimate cause of variation in growth rate, and variation in growth rate is the proximate cause of sexual size allometry. Taken together, our results provide compelling evidence in support of the sexual selection hypothesis for Rensch''s rule and highlight the potential importance of individual growth modification in the shaping of morphological patterns in Nature.     

Variability of a consistent trait: The size of the white wing patch in European Stonechats (Saxicola rubicola rubicola)

Numerous bird species exhibit striking white patches on their plumages that have been reported as signals of individual quality in the context of sexual selection. Whereas differences in white plumage traits between individuals have been well studied, phenotypic variation and the factors affecting their consistency within the individual have received less attention. Here, we studied the consistency in the size of the white wing patch and its components of variation in a Spanish population of European Stonechats Saxicola rubicola rubicola monitored over 6 years (2007–2012). The wing patch was larger in males than in females for all age-classes, and first-year individuals exhibited smaller wing patches than older birds, particularly males. This trait also varied within the plumage-year at both population and individual level, with slight changes from the moulting period to the breeding season and a sharp decrease afterwards. In addition, patch size varied both between and within individuals across years. The daily mean temperature experienced in the month immediately prior to the moult (i.e. May) had a positive effect on male wing patch size. In females, however, no variable was found to explain wing patch variation satisfactorily. Despite being a dynamic trait throughout the moults, baseline and adjusted repeatabilities indicated a moderately high consistency for white wing patch size in both sexes. Therefore, the white wing patch in Stonechats is a dynamic trait that changes throughout individuals' lives, but is also a consistent trait at the individual level. These results indicate that this depigmented patch could convey information about both the long-term quality and the current state of individuals, harmonizing the existence of intra-individual changes in the size of sexual traits with its potential role as a genetic quality indicator.     

Qualitative population divergence in proximate determination of a sexually selected trait in the collared flycatcher

We examined proximate determination of sexually selected forehead patch size in a Central‐European population of Ficedula albicollis, the collared flycatcher, using a 9‐year database, and compared our results with those obtained in other populations of the same and the sister species. Between‐individual variation of forehead patch size was large, its repeatability larger than, and heritability similar to the Swedish population. Unlike in the other populations, the trait proved unaffected by body condition, and only very slightly influenced by age. There was no relationship between forehead patch size and breeding lifespan, and a marginal negative association with survivorship in adult males. Our results suggest that additive genetic variance of the trait in this population is large, but genes act independently of body condition, and there is no viability indicator value of the trait. This is the first report of a qualitative intraspecific difference in proximate determination of a sexually selected trait.     

POPULATION DIVERGENCE IN SEXUAL ORNAMENTS: THE WHITE FOREHEAD PATCH OF NORWEGIAN PIED FLYCATCHERS IS SMALL AND UNSEXY

Models of sexual selection suggest that populations may easily diverge in male secondary sexual characters. Studies of a Spanish population of the pied flycatcher, Ficedula hypoleuca, and a Swedish population of the closely related collared flycatcher, F. albicollis, have indicated that the white forehead patch of males is a sexually selected trait. We studied the white forehead patch of male pied flycatchers (n = 487) in a Norwegian population over seven years. Males with large forehead patches were in general more brightly colored, but patch height was not correlated to body mass, body size, or parasite loads. Conditions during the nestling period did not seem to influence patch height as an adult. Patch height increased slightly from the first to the second year as adults, but then remained relatively constant at higher ages. Patch height was not related to survival. Year-to-year changes showed that males who increased in patch height also increased in body mass, suggesting that expression of the forehead patch may be partly condition dependent. However, changes in body mass explained only a small proportion of the variance in patch height between males. Thus, patch height would not be a good indicator of male quality. Furthermore, patch size was also not related to male ability to feed nestlings, indicating that females would not obtain direct benefits by choosing males with large patches. However, patch height could be a Fisher trait, but this requires heritability and there was no significant father-son resemblance in patch height. Comparisons of the males visited by each female during the mate sampling period indicated that chosen males did not have larger forehead patches than rejected males. Experimental manipulation of patch height did not affect male mating success. These results indicate that females do not use patch size as a mate choice cue. Finally, patch height did not predict the outcome of male contests for nestboxes, suggesting that the forehead patch is not an intrasexually selected cue of status. Norwegian pied flycatchers have smaller forehead patches than both Spanish pied flycatchers and Swedish collared flycatchers. We suggest that this pattern may be explained by the lack of sexual selection on the forehead patch in the Norwegian population as compared to the other populations, where the patch is apparently sexually selected. We discuss possible reasons for these population divergences, such as female choice on an alternative secondary sexual character (general plumage color) and speciation among Ficedula flycatchers.     

Sexual Selection on a Coloured Ornament in King Penguins

Species in which the sexes equally exhibit colourful ornaments are an issue for evolutionary theory. Among several hypotheses, sexual selection for mutual mate choice and social selection for signals of behavioural dominance are most commonly supported. We examined the previously documented sex‐similar size of yellow‐orange ear patches in the king penguin, Aptenodytes patagonicus. This species is monogamous and pairs just before reproduction. Raising a chick requires considerable effort by both parents, as they alternate care of their single offspring with foraging at sea. The size of the ear patches appears to signal aggressive territoriality in the breeding colony for both sexes. However, experiments suggest that females prefer large patch size during mate choice, and males do not prefer this trait. We tested whether the size of the coloured ear patch was influenced by sexual selection for couples that had recently paired. We used analyses of covariance to compare the size of the ear patch to a measure of body size and then tested for the difference between males and females. Males were 6.2% larger in ear patch width and 7.7% larger in ear patch area than females, and the distance between the ear patches over the head was 7.5% smaller in males, with all differences highly significant. Consequently, sexual selection appears to favour larger ear patches in males, possibly because of an excess of males that promotes female choice. Social selection also appears to favour the evolutionary maintenance of ear patches of males, and thus both types of selection may contribute to enlarged ear patches.     

Does experience with competition matter? Effects of source competitive environment on mean and plastic trait expression in Erodium cicutarium

Interspecific competition is likely to act as an agent for selection on local scales, although evidence in plants is sparse so far. We hypothesize that in annual shade-avoiding grassland species, heterogeneity in the intensity of aboveground competition for light may shape patterns of genetic variation and induce phenotypic plasticity in traits affecting competitive ability. We collected maternal seed families of Erodium cicutarium from replicated high and low competition environments and exposed them to different levels of aboveground competition in a glasshouse. We examined effects of seed source and competition treatment on expression of plant traits related to competitive ability and fitness. Source environments with high levels of competition were significantly more heterogeneous in competition intensity at both intermediate (approx. 10 m) and small (approx. 0.1 m) spatial scales. Seed source and competition treatment both had highly significant effects on trait expression. Greater intensity of competition experienced by maternal plants was coupled with lower vegetative biomass production and slower growth rates, and at the same time lower abortion rates in the offspring. We interpret these findings as an indication of greater reproductive efficiency in the next generation, in response to competition experienced by parents. There was higher total phenotypic variability in the plants from high competition source sites, but equivalent levels of phenotypic plasticity across source-site competition levels; no costs of phenotypic plasticity were detected. We concluded that differences in competition intensity can lead to trait differentiation in the next generation. For E. cicutarium, experience with competition matters: it leads to substantial phenotypic differences and more total variability in the offspring generation.     

Warning signal plasticity in hibiscus harlequin bugs

Color variation in aposematic (conspicuous and defended) prey should be suppressed by frequency-based selection by predators. However selection of color traits is confounded by the fact that coloration also plays an important role in many biological processes, and warning coloration may be constrained by biotic or abotic factors. Temperature, in particular the importance of thermoregulation, has been suggested as the source of much of the geographical variation in warning coloration we see in natural populations. Differential selection in different thermal environments may lead to developmentally canalized or ‘fixed’ differences between populations. Conversely, inter-population differences may be due to phenotypic plasticity, wherein trait expression is modified by environmental conditions. The hibiscus harlequin bug Tectocoris diophthalmus (Heteroptera: Scutelleridae), is a shieldback bug, with iridescent patches that show size variation between individuals, as well as inter-population variation with geographic patterning. This study aimed to identify environmental factors that drive the expression of this variable trait, using surveys, modeling, and experimental approaches. Surveys were taken at sites throughout Australia in three climate regions (tropical, subtropical, and temperate) at different time periods, and results were modeled with a multilevel ordinal regression. We tested for correlations between colouration and several biotic (density, host plant) and abiotic (temperature, rainfall) factors. We found strong phenotypic plasticity with respect to temperature and rainfall. Higher temperatures and increased rainfall were related to suppressed iridescence. A factorial experiment with tropical and temperate bugs in two climate-typical temperature regimes confirmed phenotypic plasticity in response to temperature, likely due to temperature sensitivity in melanin expression. Tropical and temperate populations showed striking differences between plasticity reaction norms, suggesting local evolution on the shape of phenotypic plasticity. We suggest that studying both biotic and abiotic selection pressures is important for understanding the causes of inter-population variation in aposematic signals.     

Assortative mating can limit the evolution of phenotypic plasticity

Phenotypic plasticity, the ability to adjust phenotype to the exposed environment, is often advantageous for organisms living in heterogeneous environments. Although the degree of plasticity appears limited in nature, many studies have reported low costs of plasticity in various species. Existing studies argue for ecological, genetic, or physiological costs or selection eliminating plasticity with high costs, but have not considered costs arising from sexual selection. Here, we show that sexual selection caused by mate choice can impede the evolution of phenotypic plasticity in a trait used for mate choice. Plasticity can remain low to moderate even in the absence of physiological or genetic costs, when individuals phenotypically adapted to contrasting environments through plasticity can mate with each other and choose mates based on phenotypic similarity. Because the non-choosy sex (i.e., males) with lower degrees of plasticity are more favored in matings by the choosy sex (i.e., females) adapted to different environments, directional selection toward higher degrees of plasticity is constrained by sexual selection. This occurs at intermediate strengths of female choosiness in the range of the parameter value we examined. Our results demonstrate that mate choice is a potential source of an indirect cost to phenotypic plasticity in a sexually selected plastic trait.     

Spatial variation in the temporal change of male and female melanic ornamentation in the barn owl

Because the magnitude of selection can vary between sexes and in space and time, sexually antagonistic selection is difficult to demonstrate. In a Swiss population of barn owls (Tyto alba), a heritable eumelanic colour trait (size of black spots on ventral feathers) was positively selected with respect to yearling survival only in females. It remains unclear whether the absence of negative selection in males is typical in this species. To tackle this issue indirectly, we measured the size of black spots in 1733 skin specimens collected by museums from 1816 to 2001 in seven European countries and in the Middle-East. The temporal change in spot size was sex- and country-specific. In males, spots became smaller particularly in three countries (Middle-East, Italy and Switzerland). In females, the size of spots increased significantly in two countries (UK and Spain) and decreased in two others (Germany and Switzerland). Because migration and phenotypic plasticity cannot explain these results, selection is the most likely cause. The weaker temporal change in spot size in females than males may be because of the combined effect of strong genetic correlation between the sexes and stronger negative selection in males than positive selection in females. We thus suggest that in the barn owl, spot size (or genetically correlated traits) is sexually antagonistically selected and that its pattern of selection may account for the maintenance of its variation and sexual dimorphism.     

Predator‐induced phenotypic plasticity in tadpoles: extension or innovation?

Phenotypic plasticity, the ability of a trait to change as a function of the environment, is central to many ideas in evolutionary biology. A special case of phenotypic plasticity observed in many organisms is mediated by their natural predators. Here, we used a predator-prey system of dragonfly larvae and tadpoles to determine if predator-mediated phenotypic plasticity provides a novel way of surviving in the presence of predators (an innovation) or if it represents a simple extension of the way noninduced tadpoles survive predation. Tadpoles of Limnodynastes peronii were raised in the presence and absence of predation, which then entered a survival experiment. Induced morphological traits, primarily tail height and tail muscle height, were found to be under selection, indicating that predator-mediated phenotypic plasticity may be adaptive. Although predator-induced animals survived better, the multivariate linear selection gradients were similar between the two tadpole groups, suggesting that predator-mediated phenotypic plasticity is an extension of existing survival strategies. In addition, nonlinear selection gradients indicated a cost of predator-induced plasticity that may limit the ability of phenotypic plasticity to enhance survival in the presence of predators.     

THE EVOLUTION OF SEXUAL DIMORPHISM BY SEXUAL SELECTION: THE SEPARATE EFFECTS OF INTRASEXUAL SELECTION AND INTERSEXUAL SELECTION

Libellula luctuosa, a pond dragonfly found in eastern North America, is apparently sexually dimorphic. Previous studies of the mating behavior in this species suggested that both male-male competition and female mate choice are important influences. Males compete for territories, where they attract females and where mating occurs. Female behavior influences both the copulation success and the fertilization success of males. Because of temporal and spatial separation of these episodes of sexual selection, multivariate and nonparametric statistical techniques could be used to investigate the influence of components of sexual selection on various sexually dimorphic traits. Sexual dimorphism in L. luctuosa was first quantified; then the direct effects and the form of selection were estimated. Sexually dimorphic wing size, body size, wing coloration, and body coloration are distributed either continuously or discontinuously between the sexes in L. luctuosa. These traits have apparently diverged between the sexes as a result of directional sexual selection. Body size is further influenced by stabilizing selection. Intrasexual selection (success in gaining access to a territory) and intersexual selection (success in copulation and fertilization) can influence the same or different sexually dimorphic characters. Body size is influenced by directional selection during the intrasexual phase of sexual selection and is also influenced by stabilizing selection during intersexual selection. The size of the brown wing patch is influenced by directional selection, primarily during the intersexual phase of sexual selection. There is directional selection on the white wing patch during both phases. Thus, the different proximate mechanisms of sexual selection may jointly or separately affect the evolution of sexually dimorphic characters. Further empirical and theoretical investigations into the differences in the effects of intrasexual selection and intersexual selection are needed to clarify the circumstances leading to separate consequences of these two mechanisms of sexual selection.