SEXUAL SELECTION,SPACE, AND SPECIATION

A Fisherian model of sexual selection is combined with a diffusion model of mate dispersal to investigate the evolution of assortative mating in a sympatric population. Females mate with one of two types of polygynous males according to a male's display of one of two sex-limited, autosomal traits; these male traits may be associated with differential phenotypic mortalities. Through a Fisherian runaway process, female preferences and male traits can become associated in linkage disequilibrium, leading to patterns of assortative mating. Dispersing males, whose rate of movement is dependent on mating success, carry female preference genes with them, and displaced males thereby produce daughters with preference genes for their respective traits in locally higher than average frequencies. The reduced diffusion of the more preferred males permits the success of other male types in adjacent areas. Thus, mating-success dependent diffusion, when coupled with the rapid divergence in phenotypes possible under the Fisher process, can lead to the coexistence of two female preferences and two male traits in sympatry. We argue that many existing approaches to sympatric speciation fail to explain observed male polymorphisms because they exclude explicit spatial structure from their speciation models.     

动物的性选择

有性生殖为个体之间设置了一个冲突和竞争的环境,因为雌雄个体都希望最大限度地把自己的基因传递给后代。性选择保证了动物的繁殖成功。性选择可以分为性别内选择和性别间选择。性别内选择促使动物格斗器官或其他有利于在格斗中获胜的一些特征得到发展;性别间选择促使用来吸引异性的一些特征得到发展。雌性动物的配偶选择或与所选择的特征协同进化,或可以从选择中得到直接的利益。     

Why birds eat colourful grit: colour preferences revealed by the colour of gizzard stones

Colour preferences from sexual or social contexts are assumed to have arisen owing to preferences for specific kinds of food, representing a sensory bias, but once colour preferences have evolved in a sexual context, they may also be expressed during foraging. We tested whether preferences for specific body colours (i.e. plumage and soft parts) were related to colour preferences for grit ingested by birds. Birds eat grit to facilitate break down of food by the gizzard, and this function is independent of the colour of grit, but depends on the physical properties of stones. Bird species were significantly consistent in colour of grit, and grit of different colours varied in prevalence among species, even when analyses were restricted to a sample from a single locality. There were positive correlations between presence of lilac and red grit in the gizzard and presence of sexually dichromatic lilac and red colour on the body. There was a positive correlation between red grit colour and red sexually monochromatic body colour. Bird species with many different sexual colours, but not sexually monochromatic colours on their body had many different colours of grit. Males had more lilac and red grit than females, with this effect differing among species, whereas that was not the case for grit of other colours. These findings are consistent with the sensory bias hypothesis that birds express preferences for grit of specific colours and a high diversity of colours related to sexual colouration of the body, even when the colour of such grit is only visible to the individual at the moment of ingestion.     

A Test for Female Attraction to Male Orange Coloration in Poecilia picta

Examining the distribution of female preference and attractive male secondary sexual characters in closely related species can help evaluate the various models for the evolution of female preference. We examined whether orange coloration in males was attractive to females of Poecilia picta, a species in the same subgenus as the guppy, P. reticulata. Females did not respond differently to males with or without a conspicuous orange stripe on the dorsum of the tail, a characteristic ornamentation of the male of this species. This lack of preference in a taxon that possesses a conspicuous, secondary sexual character directly contradicts the predictions of the sensory exploitation hypothesis for the evolution of female preference, but may support a model of antagonistic sexual selection proposed by Rice (1996).     

Evolution of female mating preferences in stalk-eyed flies

Sensory exploitation predicts that female mate preferences existbefore the evolution of exaggerated male ornaments. We testedthis prediction by estimating female preference functions, rematingintervals, and copulation durations for three species of stalk-eyedflies. Two species, Cyrtodiopsis whitei and C dalmanni, exhibitextreme sexual dimorphism in eye span, with eye stalks exceedingbody length in large males. In contrast, C quinqucguttata ofboth sexes possess short eye stalks. Maximum parsimony analysisof 437 basepairs of the 16S mitochondrial ribosomal RNA genefrom 6 Malaysian diopsids reveals that short, sexually monomorphiceye stalks are plesiomorphic in Cyrtodiopsis. Observations ofmultiple copulations by females in paired-choice mating chambersindicated that female C whitei and C. dalmanni exhibit relativepreferences for longer eye stalks such that preference intensityincreases linearly with the difference in eye stalk length betweenmales. Females from the sexually monomorphic species showedno detectable preference for male eye stalk length. Female matingpreferences of bodi sexually dimorphic species exhibited significantrepeatability, as expected if genetic variation underlies thepreference. In addition, female C whitei and C. dalmanni exhibitedshorter copulations, mated more frequently, and rejected fewermating attempts than female C quinqueguttata. Thus, opportunitiesfor sperm competition have increased with acquisition of femalepreferences. We conclude that female sensory bias for maleswith long eye span did not exist in a common ancestor to thesespecies. Instead, female preference and remating propensityeither coevolved with eye span dimorphism or evolved after maleeye stalks elongated.     

Fisherian and “good genes” benefits of mate choice: how (not) to distinguish between them

“Good genes” models of mate choice are commonly tested by examining whether attractive males sire offspring with improved survival. If offspring do not survive better (or indeed survive less well), but instead inherit the attractiveness of their father, results are typically interpreted to support the Fisherian process, which allows the evolution of preferences for arbitrary traits. Here, I show that the above view is mistaken. Because of life‐history trade‐offs, an attractive male may perform less well in other components of fitness. A female obtains a “good genes” benefit whenever males show heritable variation in quality, even if high‐quality males invest so much in sexual advertisement that attractiveness has no positive correlation with any other life‐history trait than male mating success itself. Therefore, a negative correlation between attractiveness and viability does not falsify good genes, if mating with a high‐quality male results on average in superior offspring performance (mating success of sons included). The heritable “good genes” benefit can be sustained even if sexually antagonistic genes cause female offspring sired by high‐quality males to survive and reproduce less well. Neglecting the component of male mating success from measurements of fitness returns from sons and daughters will bias the advantage of mating with a high‐quality male downwards. This result may partly account for the rather weak “good genes” effects found in a recent meta‐analysis.     

Mimicry and the evolution of premating isolation in Heliconius melpomene Linnaeus

Ecological divergence can cause speciation if adaptive traits have pleiotropic effects on mate choice. In Heliconius butterflies, mimetic patterns play a role in mate detection between sister species, as well as signalling to predators. Here we show that male butterflies from four recently diverged parapatric populations of Heliconius melpomene are more likely to approach and court their own colour patterns as compared with those of other races. A few exceptions, where males were more attracted to patterns other than their own, suggest that some mimetic patterns are sub-optimal in mate choice. Genotype frequencies in hybrid zones between races of H. melpomene suggest that mating is random, so reinforcement is unlikely to have played a role in intra-specific divergence. In summary, co-evolved divergence of colour pattern and mate preference occurs rapidly and is likely the first step in Heliconius speciation.     

The adaptive significance of electrophoretic mobility in phosphoglucose isomerase (PGI)

Sexual dimorphism in size and plumage was investigated in the lek-breeding Jackson's widowbird Euplectes jacksoni. Size dimorphism was evident from the sexual difference in tarsus length, reflecting skeletal body size. The long tail and the wide collar of breeding plumaged males were obvious secondary sex traits, but the wing was also longer than in subadults and might likewise be sexually selected (i.e. not merely a byproduct of body size). Possibly, the increased wingspan functions to save energy during the jump display. To reveal intrasexual selection, courtholders were compared with floaters (nuptial males captured off the leks), and were found to be larger in body size, wing length, collar and tail. The roles of inter-and intrasexual selection are discussed with reference to previously demonstrated female choice, and new results indicating competition for access to leks: quick reoccupation of deserted display courts, frequent observations of intruders and a finding that central males were more aggressive than peripherals. Observations imply that the collar is an agonistic signal that is neutral with respect to female choice. Possible contributions of natural selection to the sexual dimorphism are also considered.     

Genetic and environmental variation in the visual properties of bluefin killifish, Lucania goodei

Animals use their sensory systems to detect information about the external environment in order to find mates, locate food and habitat and avoid predators. Yet, there is little understanding of the relative amounts of genetic and/or environmental variation in sensory system properties. In this paper, we demonstrate genetic and environmental variation in opsin expression in a population of bluefin killifish. We measured expression of five opsins (which correlates with relative frequency of corresponding cones) using quantitative, real-time polymerase chain reaction for offspring from a breeding study where offspring were raised under different lighting conditions. Sire (i.e. genetic) effects were present for opsin found in yellow photopigment. Dam effects were present for opsins that create violet, blue and red photopigment. Lighting conditions affected expression of all opsins except SWS2A and mimicked the pattern found among populations. These results highlight the fact that sensory systems are both plastic and yet readily evolvable traits.     

The evolution of preference strength under sensory bias: a role for indirect selection?

Evidence suggests that female preferences may sometimes arise through sensory bias, and that males may subsequently evolve traits that increase their conspicuousness to females. Here, we ask whether indirect selection, arising through genetic associations (linkage disequilibrium) during the sexual selection that sensory bias imposes, can itself influence the evolution of preference strength. Specifically, we use population genetic models to consider whether or not modifiers of preference strength can spread under different ecological conditions when female mate choice is driven by sensory bias. We focus on male traits that make a male more conspicuous in certain habitats-and thus both more visible to predators and more attractive to females-and examine modifiers of the strength of preference for conspicuous males. We first solve for the rate of spread of a modifier that strengthens preference within an environmentally uniform population; we illustrate that this spread will be extremely slow. Second, we used a series of simulations to consider the role of habitat structure and movement on the evolution of a modifier of preference strength, using male color polymorphisms as a case study. We find that in most cases, indirect selection does not allow the evolution of stronger or weaker preferences for sensory bias. Only in a "two-island" model, where there is restricted migration between different patches that favor different male phenotypes, did we find that preference strength could evolve. The role of indirect selection in the evolution of sensory bias is of particular interest because of ongoing speculation regarding the role of sensory bias in the evolution of reproductive isolation.