Apostatic selection on prey that match the background

There is good experimental evidence that predators often remove disproportionately more of the common prey types. This 'apostatic selection' could maintain colour polymorphisms within prey species. In nature, morphs of many species appear to match components in the background, but most of the experiments that have tested apostatic selection have used prey that were conspicuous. In work described in this paper, wild birds at one site were presented a random order of 51 experiments. Seventeen frequencies of orange and grey pastry prey were presented on each of three types of background: a hessian sheet scattered with either orange and grey stones (the 'matching' background), or lilac and yellow stones, or green stones (two sorts of 'control' background). Each experiment consisted of four trials in succession and the numbers of the two colours eaten in each trial were recorded when about half the total prey had been eaten. Two methods of graphical analysis revealed that apostatic selection occurred on the prey on all three backgrounds, but was strongest in the grey/orange one. This last result must have been caused by some effect of the match between prey and background colour, and behavioural explanations are suggested. It is unclear whether the prey were exhibiting 'crypsis' or 'masquerade'.     

Wild birds prefer the familiar morph when feeding on pastry-filled shells of the landsnail Cepaea hortensis (Müll.)

Colour polymorphisms in prey could be maintained if predators concentrate on common morphs and confer a selective advantage on rare morphs. We describe experiments to test whether wild birds feed on pastry-stuffed shells of Cepaea hortensis in a manner that might lead to such apostatic selection. The birds were first given a 'pre-training' choice test of a shell population with equal numbers of yellow unbandeds and yellow five-bandeds; they were then trained on one morph alone, given a second choice test, trained on the other morph and, finally, given a third choice test. The birds preferred five-bandeds in five of the six pre-training tests. In all six experiments the first training session increased the birds' preferences for the morph that was familiar. The results were less clear-cut when selection during pre-training was compared with selection after the second training session. However, a comparison between selection after each of the two training sessions showed that in all six experiments the results were in the direction predicted from the hypothesis that familiar morphs are preferred. This set of experiments is one of the few in which behaviour which could lead to apostatic selection has been tested with morphs that differ in pattern. The findings support the idea that polymorphism in Cepaea could be maintained by apostatic selection.     

Natural selection for apostasy and crypsis acting on the shell colour polymorphism of a mangrove snail, Littoraria filosa (Sowerby) (Gastropoda: Littorinidae)

Littoraria filosa (Sowerby) is a member of the L. scabra group, found amongst the foliage of mangrove trees in northern Australia. The colour of the shell is polymorphic, showing two discrete ground colours, either yellow or orange-pink, with a variable degree of superimposed brown patterning. At a site on Magnetic Island, northern Queensland, colour frequencies of small snails were similar on different backgrounds. Amongst larger shells yellows were more frequent on Avicennia trees with abundant foliage, and browns on relatively bare trees, suggesting that visual selection for crypsis occurred. There was no evidence of substrate selection by the morphs. Yellow shells were cooler than brown shells, but differences in colour frequencies on sunny and shaded trees, and at different seasons, did not suggest climatic selection. By manipulating the colour frequencies of subpopulations of small snails isolated on individual trees, it was shown that the disappearance of yellow and brown shells was frequency-dependent. This result is consistent with hypotheses of mimicry of background elements by the morphs and of apostatic selection by unknown predators. Only the latter can account for the persistence of the highly conspicuous pink morph at a low frequency.     

Shell colour polymorphism in a mangrove snail Littorina sp. (Prosobranchia: Littorinidae)

Shell colour polymorphism was examined in populations of a mangrove snail Littorina sp. in Queensland, Australia. Three morphs were recognized, yellow, red and brown, and morph frequencies varied both between widely spaced populations and between islands less than 1 km apart. Morph frequencies also varied with time of year. There was a relationship between shell colour and position on the tree, with yellow snails more often occurring amongst the foliage and brown snails more often on trunks and branches. In some populations yellow snails appeared to survive better than the other morphs, while in other populations there was no difference. The evidence for the maintenance of the polymorphism by natural selection is discussed.     

Apostasy and selection for crypsis in the marine snail Littoraria filosa: an explanation for a balanced colour polymorphism

The marine snail, Littoraria filosa, is polymorphic for shell colour, with yellow, brown, and pink morphs that correspond in both appearance and frequency to the predominant background colours of its habitat. Previous research on this polymorphism has found indirect evidence of apostatic selection and selection for crypsis by unknown agents, probably crabs, and direct evidence of selection for crypsis by the parasitoid fly Sarcophaga megafilosia. In the present study, we report on field experiments to investigate whether S. megafilosia and shell‐crushing predators exert apostatic selection on L. filosa. For S. megafilosia, seven experimental treatments containing yellow and brown snails in the proportions of 0.1, 0.2, 0.4, 0.5, 0.6, 0.8, and 0.9 of each colour were established on mangrove trees and used to separately quantify the proportions of each colour attacked on grey/brown trunks and yellow/green leaves. The results obtained confirmed an earlier finding of selection for crypsis, but only showed slight, but significant, anti‐apostatic selection by S. megafilosia. For shell‐crushing predators, seven experimental treatments containing yellow and brown snails in the proportions of 0.08, 0.17, 0.33, 0.50, 0.66, 0.83, and 0.92 were established on two types of trees that differed in their background proportions of brown and green: (1) trees which had been pruned of approximately 90% of their foliage and (2) unpruned trees. The results obtained showed both selection for crypsis and apostatic selection. Furthermore, a selectively neutral frequency for yellow L. filosa was found for each background, and was less on pruned trees than unpruned ones (and vice versa for brown L. filosa), which can therefore account for the maintenance of a colour polymorphism where the proportions of each morph tend to resemble and correspond in frequency to the colours of the background. © 2008 The Linnean Society of London, Biological Journal of the Linnean Society, 2008, 95 , 62–71.     

Plumage polymorphism and fitness in Swainson’s hawks

We examine the maintenance of a plumage polymorphism, variation in plumages among the same age and sex class within a population, in a population of Swainson’s Hawks. We take advantage of 32 years of data to examine two prevalent hypotheses used to explain the persistence of morphs: apostatic selection and heterozygous advantage. We investigate differences in fitness among three morph classes of a melanistic trait in Swainson’s Hawks: light (7% of the local breeding population), intermediate (57%) and dark (36%). Specifically, we examined morph differences in adult apparent survival, breeding success, annual number of fledglings produced, probability of offspring recruitment into the breeding population and lifetime reproductive success (LRS). If apostatic selection were a factor in maintaining morphs, we would expect that individuals with the least frequent morph would perform best in one or more of these fitness categories. Alternatively, if heterozygous advantage played a role in the maintenance of this polymorphism, we would expect heterozygotes (i.e. intermediate morphs) to have one or more increased rates in these categories. We found no difference in adult apparent survival between morph classes. Similarly, there were no differences in breeding success, nest productivity, LRS or probability of recruitment of offspring between parental morph. We conclude that neither apostatic selection nor heterozygous advantage appear to play a role in maintaining morphs in this population.     

THE EVOLUTION OF EXUBERANT VISIBLE POLYMORPHISMS

Visible genetic polymorphism is a common feature of many species. In most cases, the mechanism(s) underlying the maintenance of such variation remain obscure although apostatic selection has often been suggested. Here, we explore individual-based evolutionary models to understand what features of predator–prey relationships may lead to patterns of exuberant polymorphism similar to those observed in the wild. When all morphs are equally visible, the number of evolved morphs increases with the strength of apostatic selection although even with powerful selection the number morphs is still relatively small. The introduction of dietary wariness increases the number of morphs substantially, even when apostatic selection is absent. When one morph is more cryptic the number of evolved morphs is fewer. The cryptic morph reaches high frequency in the population and other morphs are each at lower frequencies. Decreasing the predation intensity enhances the number of evolved morphs in all models. Dietary wariness is a critical factor missing from earlier models and it may provide a general solution to the problem of polymorphisms involving many morphs. Apostatic selection is shown to be neither a necessary, nor a sufficient, requirement for the maintenance of exuberant polymorphisms.     

The evolution of colour polymorphism in British winter‐active Lepidoptera in response to search image use by avian predators

Phenotypic polymorphism in cryptic species is widespread. This may evolve in response to search image use by predators exerting negative frequency‐dependent selection on intraspecific colour morphs, ‘apostatic selection’. Evidence exists to indicate search image formation by predators and apostatic selection operating on wild prey populations, though not to demonstrate search image use directly resulting in apostatic selection. The present study attempted to address this deficiency, using British Lepidoptera active in winter as a model system. It has been proposed that the typically polymorphic wing colouration of these species represents an anti‐search image adaptation against birds. To test (a) for search image‐driven apostatic selection, dimorphic populations of artificial moth‐like models were established in woodland at varying relative morph frequencies and exposed to predation by natural populations of birds. In addition, to test (b) whether abundance and degree of polymorphism are correlated across British winter‐active moths, as predicted where search image use drives apostatic selection, a series of phylogenetic comparative analyses were conducted. There was a positive relationship between artificial morph frequency and probability of predation, consistent with birds utilizing search images and exerting apostatic selection. Abundance and degree of polymorphism were found to be positively correlated across British Lepidoptera active in winter, though not across all taxonomic groups analysed. This evidence is consistent with polymorphism in this group having evolved in response to search image‐driven apostatic selection and supports the viability of this mechanism as a means by which phenotypic and genetic variation may be maintained in natural populations.     

Differential predation on sexes affects colour polymorphism of the isopod Idotea baltica (Pallas)

Variable selection, including spatio-temporal variation, frequency-dependent selection and differential selection due to habitat choice, may maintain polymorphism in heterogeneous environments. We studied predation as a selective agent on colour polymorphism of the aquatic isopod I baltica. Variable predation on this species can arise from at least three sources. First, apostatic selection was studied by testing the formation of preferences on colour morphs in the perch, a common predator of I baltica. Such acquired preferences should induce apostatic selection. While our results indicate some acquired preferences, there was significant heterogeneity in the behaviour of predator individuals. Second, temporal variation in selection can arise due to habitat shift from the green algae juvenile habitat to the bladderwrack adult habitat, and the consequent change in the crypsis of the morphs. Different crypsis between sexes probably promoted high predation mortality among females in the juvenile habitat. The high rate of male mortality during the breeding period, on the other hand, was presumably due to their high mate-searching activity. Third, the sex-dependent habitat choice of I baltica leads to sexual differences in the susceptibility of morphs to predation. Predators preferred the white-spotted morph over the uniform one in males but not in females, supporting the 'dimorphic niche' hypothesis as an explanation of sexual differences in morph frequencies. Finally, no evidence was found that the colouration patterns were under sexual selection. We therefore conclude diat variable predation is the most promising explanation for the maintenance of polymorphism in I. baltica.     

An exuberant, undescribed colour polymorphism in Theridion californicum (Araneae, Theridiidae): implications for a theridiid pattern ground plan and the convergent evolution of visible morphs

An opisthosomal (abdominal) colour polymorphism is described in the North American spider, Theridion californicum , comprising a plain Yellow morph and (at least) ten patterned morphs, which exhibit areas of red or black pigments superimposed on the yellow background, or no pigment (white). The polymorphism appears to be present throughout the species' range. The Yellow morph is the most frequent in populations, with patterned morphs all, individually, being rather rare. Progeny from known mothers were reared and indicate that the polymorphism is genetic and that Yellow is probably recessive to patterned morphs. Similar to other theridiids with well-studied colour polymorphisms, T. californicum occupies an under-leaf habitat and the variation in all these cases might be maintained by sight-hunting predators exerting negative frequency-dependent (apostatic) selection. In T. californicum , blocks of guanine underlying the pigmented hypodermis indicate a segmental patterning, which is not usually apparent in adult spiders. These segments, plus dorso-lateral divisions, permit the dorsal surface of the opisthosoma to be divided up into two mirror-image halves, each comprising 12 compartments. Each compartment can either lack pigment (thus appearing white as a result of underlying guanine) or be yellow, red, or black. All patterns in T. californicum can be derived from this ground plan, as can the morphs of other colour-polymorphic theridiids. It is suggested that selection for polymorphism, combined with constraints imposed by this theridiid ground plan, may have led to the convergent evolution of colour patterns across the family.  © 2009 The Linnean Society of London, Biological Journal of the Linnean Society , 2009, 96 , 23–34.     

Sexual selection and non-random mating for shell colour in a natural population of the marine snailLittorina mariae (Gastropoda: Prosobranchia)

In order to estimate the three independent components of mating behaviour, sexual selection in females, sexual selection in males and mating pattern, we studied the distribution of shell colour morphs among mating pairs and between copulating and non-copulating snails in four subsamples of a natural population ofL. mariae. The colour of the shell, the sex and a qualitative estimate of age was recorded for every snail. We found sexual selection acting against one of the two commonest colours (yellow) among the young females. However, in males none of the eight shell colour morphs was favoured during matings. Male sexual choice or differences in female sexual activity may cause the sexual fitness disadvantage of yellow females. Moreover, individuals of different colour morphs did not mate at random, rather dissasortatively. A behavioural choice among shell colour morphs or a non-random microdistribution of the morphs may cause the departure from random mating in this population.     

Activity and weight loss in relation to solar radiation in the polymorphic land snail Cepaea nemoralis

Shell spectral reflectance, activity and weight loss in the land snail Cepaea nemoralis were examined to test whether solar radiation has different effects on the behavioural and physiological responses of different morphs. A uniform area from the empty shells of different morphs was cut and a spectrophotometer was used to measure the spectral reflectance at wavelengths from 220 nm to 800 nm. Snails were put into cages made of mesh hardware cloth, and their activities were observed from dawn onwards on two hot, dry days. Weight loss of snails under shade and under direct sunlight was also measured.
The results show that unbanded morphs reflect more light than five-banded ones, but the yellow morphs reflect only a little more than pink morphs. Five-banded morphs became inactive more quickly than unbanded ones from dawn onwards, but the differences in activity patterns were not significant between pink and yellow morphs. There are significant differences in percent weight loss between snails placed under direct sunlight and under shade. The weight loss of different morphs under shade was not statistically different. But when exposed to sunlight, five-banded morphs lost more weight than pink and yellow unbanded morphs.
Because of their lower reflectance of solar radiation, the five-banded morphs are, in a hot, arid climate, at a selective disadvantage compared to unbanded morphs. However, they can avoid such selective disadvantage by actively seeking a shaded area, as all other morphs do in the field. Such behavioural habitat selection could help the maintenance of genetic polymorphisms in natural populations.     

Sexual selection and assortative mating by size and their roles in the maintenance of a polymorphism in Swedish Littorina saxatilis populations

Two independent components of mating behaviour, sexual selection and assortative mating, were studied in two allopatric morphs, one sheltered boulder shore form (S-morph) and one exposed cliff shore form (E-morph), of Littorina saxatilis from the west coast of Sweden. Sexual selection was studied by comparing the sizes of copulating and non-copulating snails in the field. Size assortative mating was studied by collecting copulating pairs in the field, while assortative mating between morphs was investigated by bringing the pure morphs together in intermediary habitats and then noting the matings. The S-morph mated randomly in relation to size in two of the studied populations and exhibited a trend towards size assortative mating in a third, while the E-morph showed size assortative mating in both studied populations. The microdistribution of sizes of snails on the shores could not explain all the size assortative mating found, and instead it is argued that a size-based mate rejection behaviour also contributes to the assortative mating in at least some of these populations. There was sexual selection on size in both males and females in the S-morph, with large individuals being favoured as mates. In contrast, copulating snails of the E-morph were smaller than non-copulating ones. The significantly different sexual selection intensities between the two morphs may help to explain the size differences between them. There was random mating between the E- and the S-morphs of L. saxatilis, which suggests no incipient reproductive isolation between morphs on Swedish rocky shores. This is in agreement with earlier studies of Swedish populations, but is in contrast to the situation found in other geographical areas.     

The role of selection in the colour polymorphism of Littorina rudis Maton and Littorina arcana Hannaford-Ellis (Prosobranchia: Littorinidae)

Forty-one mixed samples of winkles containing the closely related species, Littorina rudis and L. arcana , were collected from different parts of the British Isles. Littorina rudis was the more ubiquitous species, with L. arcana being more-or-less confined to vertical cliffs and rocks. The frequencies of different shell colour patterns were determined for both species in each sample. Several colour morphs were diagnostic of one or other of the species over large areas, which confirms that these are separate species. The frequencies, in the two species, of the two commonest morphs, brown and fawn, were strongly correlated; in several other morphs their presence and absence in the two species was significantly associated; the levels of phenotypic diversity in the two species were also correlated. These patterns could not have arisen if the variation between shores was the result of genetic drift or founder effects, so some form of selection is implicated. In the brown morph there is some evidence for frequency-dependent selection, and it is suggested that the polymorphism may be maintained by visual predators through apostatic selection.     

The interrelationship between crypsis and colour polymorphism

The mechanisms behind the evolution and maintenance of conspicuous visible polymorphisms comprising tens of morphs present a challenge to evolutionary theory. However, for cryptic forms Endler (Evol. Biol., 11, 1978, 319) conjectured that complex backgrounds facilitate polymorphism because in such habitats there are several ways to resemble the resting surface. We use computer simulation to explore the evolution of cryptic morphs on increasingly complex backgrounds under regimes that include selection for crypsis, apostatic predation and dietary wariness. We show that there is a monotonic increase in the number of morphs evolving in a population as the potential number of cryptic morphs increases. The relationship is very weak with selection for crypsis alone, but much stronger with the addition of apostatic selection. In contrast, when dietary wariness is added to the model the plot of number of morphs maintained, as a function of the potential number of cryptic forms available, is minimized at an intermediate number of cryptic forms, i.e. is V-shaped. These counter-intuitive patterns are robust to varying strengths of apostatic selection and different implementations of dietary wariness, and are more pronounced when predator and prey generation lengths are similar.     

Natural selection for rare and mimetic colour pattern combinations in wild populations of the diadem butterfly, Hypolimnas misippus L

Mark recapture and morph frequency data, gathered during a population irruption of Hypolimnas misippus in southern Ghana, provide evidence for apostatic and mimetic selection. During a period of low adult survival, both the recapture rate and the frequency of the commonest morph ( misippus ) were significantly reduced. Selection against this form increased phenotypic diversity and generated significant disequilibrium in the combinations of unlinked fore- and hindwing phenotypes. There was also evidence for selection against those forms (weak alcippoides ) which most closely resemble misippus . Other morphs, including both good mimics of Danaus chrysippus and rare non-mimics, showed no reductions in recapture rate during the period of low survival, but only the good mimics increased significantly in frequency. The results provide a predictive ecological model for density-dependent selection by predators which is consistent with field data from previous studies of H. misippus in Ghana and Tanzania. Their evolutionary implications are discussed, and it is suggested that anomalies in the mimicry of this species may be partly due to lack of predation when it is scarce.     

Influence of shell colour on the mortality rate of the land snail Arianta arbustorum under different microclimatic regimes

The mortality of phenotypic shell colour morphs and age classes of the snail Arianta arbustorum in several microclimatic conditions was recorded. An analysis of variance was performed on five factors: adaptation temperature, relative humidity, shell colour, age class and test temperature. There were no significant differences in the mortality between different adaptation temperatures or relative humidities, but the interaction of these two factors was highly significant. There were significant differences in mortality rate between test temperature and age class. The mortality of the brown morph was higher than the yellow one at all adaptation temperatures (overall, P < 0.05). There were no significant differences between the mortality rates of the two morphs at different relative humidities. The mortality of the brown morph was higher than that of the yellow at six out of seven test temperatures. Juvenile snails survived significantly better than adults at all test temperatures.     

Interaction between female mating preferences and predation may explain the maintenance of rare males in the pentamorphic fish Poecilia parae

Variation in mating preferences coupled with selective predation may allow for the maintenance of alternative mating strategies. Males of the South American live‐bearing fish Poecilia parae fall in one of five discrete morphs: red, yellow, blue, stripe‐coloured tail (parae) and female mimic (immaculata). Field surveys indicate that the red and yellow morphs are the rarest and that their rarity is consistent across years. We explored the role of variable female mating preference and selective predation by visual predators in explaining the rarity of red and yellow males, and more generally, the maintenance of this extreme colour polymorphism. We presented wild‐caught P. parae females and Aequidens tetramerus, the most common cichlid predator, with the five male colour morphs in separate trials to determine mating and prey preferences, respectively. We found that a large proportion of females shared a strong preference for the rare carotenoid‐based red and yellow males, but a distinct group also preferred the blue and parae morphs. The cichlid predator strongly preferred red and yellow males as prey. Together, these results suggest that the interaction between premating sexual selection favouring and predation acting against the red and yellow morphs may explain their rarity in the wild. The trade‐off between sexual and natural selection, accompanied by variation in female mating preferences, may therefore facilitate the maintenance of the striking colour polymorphism in P. parae.     

The influence of density on frequency-dependent selection by wild birds feeding on artificial prey

Previous work has demonstrated frequency-dependent selection by wild garden birds when feeding on green and brown pastry ''baits''. When the density of baits is low, the common colour is eaten disproportionately more than the rare colour (apostatic selection), and when the density is very high, the rare colour is eaten disproportionately more than the common (anti-apostatic selection). We explored the relationship between frequency-dependent predation and density in an experiment at 16 separate sites, using four levels of density and two frequencies of green and brown. Analysis of estimates of log-relative risk ratios showed little evidence for frequency-independent selection, but frequency-dependent selection changed gradually from apostatic at low density to anti-apostatic at high density. The validity of these conclusions in terms of individual bird behaviour was confirmed by Monte-Carlo simulations. We thus conclude that selection by wild birds feeding on green and brown artificial prey is frequency dependent, and that the strength and direction of this selection changes with prey density in a gradual and predictable manner.     

SOCIAL CAUSES OF CORRELATIONAL SELECTION AND THE RESOLUTION OF A HERITABLE THROAT COLOR POLYMORPHISM IN A LIZARD

Abstract When selection acts on social or behavioral traits, the fitness of an individual depends on the phenotypes of its competitors. Here, we describe methods and statistical inference for measuring natural selection in small social groups. We measured selection on throat color alleles that arises from microgeographic variation in allele frequency at natal sites of side‐blotched lizards (Uta stansburiana). Previous game‐theoretic analysis indicates that two color morphs of female side‐blotched lizards are engaged in an offspring quantity‐quality game that promotes a density‐and frequency‐dependent cycle. Orange‐throated females are r‐strategists. They lay large clutches of small progeny, which have poor survival at high density, but good survival at low density. In contrast, yellow‐throated females are K‐strategists. They lay small clutches of large progeny, which have good survival at high density. We tested three predictions of the female game: (1) orange progeny should have a fitness advantage at low density; (2) correlational selection acts to couple color alleles and progeny size; and (3) this correlational selection arises from frequency‐dependent selection in which large hatchling size confers an advantage, but only when yellow alleles are rare. We also confirmed the heritability of color, and therefore its genetic basis, by producing progeny from controlled matings. A parsimonious cause of the high heritability is that three alleles (o, b, y) segregate as one genetic factor. We review the physiology of color formation to explain the possible genetic architecture of the throat color trait. Heritability of color was nearly additive in our breeding study, allowing us to compute a genotypic value for each individual and thus predict the frequency of progeny alleles released on 116 plots. Rather than study the fitness of individual progeny, we studied how the fitness of their color alleles varied with allele frequency on plots. We confirmed prediction 1: When orange alleles are present in female progeny, they have higher fitness at low density when compared to other alleles. Even though the difference in egg size of the female morphs was small (0.02 g), it led to knife‐edged survival effects for their progeny depending on local social context. Selection on hatchling survival was not only dependent on color alleles, but on a fitness interaction between color alleles and hatchling size, which confirmed prediction 2. Sire effects, which are not confounded by maternal phenotype, allowed us to resolve the frequency dependence of correlational selection on egg size and color alleles and thereby confirmed prediction 3. Selection favored large size when yellow sire alleles were rare, but small size when they were common. Correlational selection promotes the formation of a self‐reinforcing genetic correlation between the morphs and life‐history variation, which causes selection in the next density and frequency cycle to be exacerbated. We discuss general conditions for the evolution of self‐reinforcing genetic correlations that arise from social selection associated with frequency‐dependent sexual and natural selection.