Group selection in plant populations

Summary Several mechanisms have been proposed for group selection, to account for the evolution of altruistic traits. One type, Neighbourhood models, suggests that individuals react with those immediately around them, but with no recognition mechanism. The organization of plant populations seems especially favorable for this type of selection. The possibility of Neighbourhood selection was investigated by simulating a plant population. It was possible for an altruistic trait to evolve, though only under restricted conditions. The main requirement was gene flow only by very restricted pollen dispersal, and a high benefit : cost ratio in the altruistic relationship. Under conditions favourable for such evolution, the starting frequency of the allele, the initial pattern, and the population size, had little effect. Inbreeding tended to prevent the increase of the altruism allele, though this depended on the mechanism of selfing. Known ecological features of plants are discussed that could be considered altruistic and hence require some form of group selection for their evolution, and whether the benefit : cost requirements are likely to be met. Neighbourhood models of group selection are a possibility in plant populations, and we therefore cannot exclude the possibility of altruism in plants. However, Neighbourhood selection is weak force, unlikely to be effective in the face of opposing individual selection. It may be more important as reinforcement of individual selection.     

The Coalescent Time in the Presence of Background Fertility Selection

Selection ultimately entails differential reproductive success over several generations. This can be measured as a correlation of the number of progeny an individual has with the number of progeny its parent had. This correlation could have a genetic or a cultural basis. The effect of such a correlation is to multiply the single generation sampling variance (Vdeltap) in the diffusion approximation for fixation time by (1-b)+bx(1+r)/(1-r), where bxrn is the correlation between the number of progeny of an individual and its ancestor n generations ago (e.g., b is the heritability and br is the resultant parent-offspring progeny number correlation if the progeny number is genetically determined). This results in a reduction of the fixation or coalescent time by division by this factor. Sex differences in this correlation have been observed, and this provides an explanation for the difference of coalescent times of y-chromosomes and mitochondria.     

Antler size and fluctuating asymmetry in red deer (Cervus elaphus) stags and probability of becoming a harem holder in rut

Red deer hinds play a significant role in selecting stags for mating. We tested the hypotheses that in red deer ( Cervus elaphus ) the probability of becoming a harem holder (and hence achieving reproductive success) occurs in stags bearing larger, branched antlers and showing low fluctuating asymmetry (FA). Eleven antler characteristics were measured; absolute and relative FA were calculated on 51 cast antler sets from 19 individually recognized stags. Probability of becoming a harem holder (PBHH) was originally analysed separately, i.e. for antler size and FA of each antler characteristic and calculated factors for both antler size and FA. If analysed separately, large antler size and low relative but high absolute FA increased PBHH. When we combined antler size and FA of antler characteristics in one model using antler size and FA factors, however, PBHH and achieving reproductive success were mainly dependent on increasing antler size and enhanced antler branching rather than on FA. We conclude that in contrast to antler size, FA is unlikely to play any significant role in sexual selection as an indicator of individual quality.  © 2006 The Linnean Society of London, Biological Journal of the Linnean Society , 2006, 87 , 59–68.     

Sex differences in survival selection in the serin,Serinus serinus

Natural selection is demonstrated in most natural populations which suggests that populations are dispatched from their adaptive peaks as a result of selection on correlated characters, or conflicting selection between the sexes. We analysed patterns of survival selection in a population of serins (Serinus serinus) outside Barcelona over a period of 13 years. There was directional selection for increased wing length in males and females accompanied by strong disruptive selection on both tail and wing length in males and a selection against a positive correlation between the two characters in males. In females there was directional selection for increased bill width but decreased bill depth, which should be contrasted to the stabilizing selection acting on bill depth in males. There were conflicting selection on the characters within a sex and conflicting selection of the same characters between sexes, which constrain the rate of access to the nearest adaptive peak.     

Repeatability of size and fluctuating asymmetry of antler characteristics in red deer (Cervus elaphus) during ontogeny

Fluctuating asymmetry (FA) has been suggested as a measure of the sensitivity of development to a wide array of genetic and environmental stresses. It has been also suggested that antlers in red deer could be important during social and rutting displays. We used antler measurements of 51 males that were measured over subsequent seasons, from 3–8 years of age, and analysed three antler traits: antler weight, length, and the number of antler tines (antler size). We calculated absolute and relative FA. All three size traits were highly significantly intercorrelated. By contrast to this, the FA of the three traits, did not show such relationships. With increasing age, antler size and FA also increased. When testing the repeatability of FA and antler size, there was a principal difference in the pattern between FA and antler size, with the latter being much more consistent than the former. This suggests that antler size, not FA, may be a good predictor of the bearer's quality in mate selection. This fits well with the good-genes hypothesis that the development of extravagant secondary sexual characters can be an honest advertisement of heritable male quality.  © 2007 The Linnean Society of London, Biological Journal of the Linnean Society , 2007, 91 , 215–226.     

Selection index for identifying high-yielding groundnut genotypes in irrigated and rainfed environments

Selection of high yielding genotypes to be carried over to subsequent selection cycles in a breeding programme can sometimes be accomplished using a suitable index of secondary traits that may be relatively less sensitive to genotype‐by‐environment interactions than yield. We used the concept of correlated response to selection to measure the relative efficiency of nine selection indices. The results showed that the selection index, based on median and semi inter‐quartile range, which was actually used in identifying high yielding genotypes, had an efficiency that is comparable to the best index, the latter being a modification of the Elston index.     

黑眶蟾蜍的两性异形与选型配对模式

本研究以黑眶蟾蜍(Duttaphrynus melanostictus)为研究对象,通过对比黑眶蟾蜍抱对个体的体长、头长、头宽、眼间距、鼓膜径、耳后腺长、眼径、前臂及手长、前肢长以及后肢长等形态特征,分析雌性黑眶蟾蜍繁殖输出与其体型的关系,探究黑眶蟾蜍两性异形模式及其与雌性生育力的关系;同时通过对配对个体形态学特征的相关性分析探究了黑眶蟾蜍的配对模式。结果表明,黑眶蟾蜍雌性体长和体重显著大于雄体;两性的所有局部形态特征均与体长成正相关;去除体长因素影响后,雄性头长以及后肢长均明显大于雌性,其余局部形态特征两性间则皆无显著差异。雌体的窝卵重、窝卵数均与其体长和体重成正相关关系。雌性成体的前肢长与抱对雄性成体的前肢长之间呈显著正相关,其余形态特征两性间均无相关性。研究表明,生育力选择是导致黑眶蟾蜍两性异形的重要驱动力;黑眶蟾蜍的选型配对模式未表现在个体大小上,而是体现在局部特征(前肢长),这不仅为揭示两栖类配对模式的普遍性提供了参考,还表明对两栖类选型配对的研究应以多个性状为对象。     

Spatiotemporal variation in selection on body size in the dung fly Sepsis cynipsea

Standardized measures of the strength of selection on a character allow quantitative comparisons across populations in time and space. Spatiotemporal variation in selection influences patterns of adaptation and the evolution of characters and must therefore be documented. For the dung-breeding fly Sepsis cynipsea, we document patterns of variation in sexual, fecundity and larval and adult viability selection on body size at several spatiotemporal scales: between-populations, over the season, over the day and between dung pats. Adult viability selection based on residual physiological survivorship in the laboratory was nil or weakly negative. In contrast, larval viability selection in two laboratory environments was weakly positive for males at low competition and females at high competition. Fecundity selection was positive and strong at all times and in all populations. Sexual selection reflecting pairing success was overall strongly positive (about three times stronger than fecundity selection), while selection reflecting male reproductive success via the clutch size of his mate (i.e. assortative mating) was essentially nil. Only sexual selection varied significantly at coarse (between populations and seasonally) but not at fine (within a day or between pats on a pasture) spatial and temporal scales. Quadratic and correlational selection differentials were low and inconsistent in all episodes except for fecundity selection, where there was some evidence that clutch size reaches an asymptote at large body sizes, implying weaker selection for large size as females get bigger. Implications of these results for the evolution of body size and body size dimorphism are discussed.     

Sexual selection and temporal phenotypic variation in a damselfly population

Temporal variation in selection can be generated by temporal variation in either the fitness surface or phenotypic distributions around a static fitness surface, or both concurrently. Here, we use within- and between-generation sampling of fitness surfaces and phenotypic distributions over 2 years to investigate the causes of temporal variation in the form of sexual selection on body size in the damselfly Enallagma aspersum. Within a year, when the average female body size differed substantially from the average male body size, male body size experienced directional selection. In contrast, when male and female size distributions overlapped, male body size experienced stabilizing selection when variances in body size were large, but no appreciable selection when the variances in body size were small. The causes of temporal variation in the form of selection can only be inferred by accounting for changes in both the fitness surface and changes in the distribution of phenotypes.     

Stronger convex (stabilizing) selection on homologous sexual display traits in females than in males: a multipopulation comparison in Drosophila serrata

Mutual mate choice for homologous sexual display traits has been demonstrated in several recent studies yet little attention has been given to quantitative comparison of the strength and form of mate preferences between the sexes. Such comparisons may provide important insight into the evolution of mate choice for honest signals. In particular, because females generally provide the majority of resources for initial offspring development, female displays may trade-off with fecundity, causing preference evolution to differ between the sexes. Recent theory suggests that adaptive male preferences for honest displays in females are possible under certain conditions and may result in preferences that are convex (i.e., stabilizing) in form. We compared sexual selection on a suite of contact pheromones arising from mutual mate choice using nine separate geographic populations of Drosophila serrata. We show that the convex selection is stronger on females than on males overall in these populations, and that convex selection is the predominate form of nonlinear selection on females but not males.     

Sexual selection is stabilizing selection in pupfish [Cyprinodon pecosensis)

One of the predictions of the 'good genes' model of sexual selection is that reproductively successful males with well-developed indicator traits should show smaller variances for non-indicator traits, that are not directly associated with mating success, when compared to non-breeding males and females. Thus sexual selection should reinforce stabilizing natural selection in reducing the variance in quantitative traits. This prediction is tested by analysing variation in eight morphological traits of breeding males, non-breeding males, and females of pupfish (Cyprinodon pecosensis). Breeding males tended to be less variable than non-breeding males for all principal component factors, and for all morphological traits except for depth, although these differences were statistically significant only for PC2, and PC5 and for pelvic fin length, number of pelvic fin rays and number of preopercular and preorbital pores. Similarly, breeding males tended to be less variable than females for all principal component factors and for all morphological traits except for number of preopercular pores. These differences were statistically significant for PC2, and for depth, pelvic fin length, number of preorbital pores and pectoral fin rays. The overall pattern of reduced variability in independent traits of breeding males revealed by principal component analysis is very consistent and highly significant (P<10⁵). These results support the prediction of the 'good genes' model and show that reproductively active males are subject to more severe stabilizing selection for several quantitative traits than non-breeding males and females. Thus sexual selection, through male-male competition, female choice, or an interaction of both selective processes, results in stabilizing selection on quantitative morphological traits.     

The form of sexual selection arising from male-male competition depends on the presence of females in the social environment

Sexual selection arises from social interactions, and if social environments vary so too should sexual selection. For example, male-male competition often occurs either in the presence or in the absence of females, and such changes in the social environment could affect the form and strength of sexual selection. Here we examine how the presence of a female influences selection arising from male-male competition in a leaf-footed cactus bug, Narnia femorata, which has a resource defence mating system. Males compete for territories on cacti because females lay eggs on the cactus plants. Females are not always present when this competition first occurs; however, the presence or absence of the female matters. We found that both the form and strength of selection on male traits, those traits that influenced success in intrasexual competition, depended on the social context. When a female was not present, male size and the area of the sexually dimorphic hind legs was only marginally important to winning a contest. However, males with larger overall size and leg area were more likely to win in the presence of a female. There was also positive quadratic selection on these traits when a female was present with both the largest and the smallest males winning. The implication is unexpected alternative strategies when females are present. Our results support the notion that sexual selection should be studied under all relevant social contexts.     

Field and experimental evidence for competition's role in phenotypic divergence

Resource competition has long been viewed as a major cause of phenotypic divergence within and between species. Theory predicts that divergence arises because natural selection favors individuals that are phenotypically dissimilar from their competitors. Yet, there are few conclusive tests of this key prediction. Drawing on data from both natural populations and a controlled experiment, this paper presents such a test in tadpoles of two species of spadefoot toads (Spea bombifrons and S. multiplicata). These two species show exaggerated divergence in trophic morphology where they are found together (mixed-species ponds) but not where each is found alone (pure-species ponds), suggesting that they have undergone ecological character displacement. Moreover, in pure-species ponds, both species exhibit resource polymorphism. Using body size as a proxy for fitness, we found that in pure-species ponds disruptive selection favors extreme trophic phenotypes in both species, suggesting that intraspecific competition for food promotes resource polymorphism. In mixed-species ponds, by contrast, we found that trophic morphology was subject to stabilizing selection in S. multiplicata and directional selection in S. bombifrons. A controlled experiment revealed that the more similar an S. multiplicata was to its S. bombifrons tankmate in resource use, the worse was its performance. These results indicate that S. multiplicata individuals that differ from S. bombifrons would be selectively favored in competition. Our data therefore demonstrate how resource competition between phenotypically similar individuals can drive divergence between them. Moreover, our results indicate that how competition contributes to such divergence may be influenced not only by the degree to which competitors overlap in resource use, but also by the abundance and quality of resources. Finally, our finding that competitively mediated disruptive selection may promote resource polymorphism has potentially important implications for understanding how populations evolve in response to heterospecific competitors. In particular, once a population evolves resource polymorphism, it may be more prone to undergo ecological character displacement.     

Lifetime selection on adult body size and components of body size in a waterstrider: opposing selection and maintenance of sexual size dimorphism

Abstract.— Sexual size dimorphism (SSD), the difference in body size between males and females, is common in almost all taxa of animals and is generally assumed to be adaptive. Although sexual selection and fecundity selection alone have often been invoked to explain the evolution of SSD, more recent views indicate that the sexes must experience different lifetime selection pressures for SSD to evolve and be maintained. We estimated selection acting on male and female adult body size (total length) and components of body size in the waterstrider Aquarius remigis during three phases of life history. Opposing selection pressures for overall body size occurred in separate episodes of fitness for females in both years and for males in one year. Specific components of body size were often the targets of the selection on overall body size. When net adult fitness was estimated by combining each individual's fitnesses from all episodes, we found stabilizing selection in both sexes. In addition, the net optimum overall body size of males was smaller than that of females. However, even when components of body size had experienced opposing selection pressures in individual episodes, no components appeared to be under lifetime stabilizing selection. This is the first evidence that contemporary selection in a natural population acts to maintain female size larger than male size, the most common pattern of SSD in nature.     

Diversifying and Purifying Selection in the Peptide Binding Region of <Emphasis Type="Italic">DRB</Emphasis> in Mammals

The class II genes of the major histocompatibility complex encode proteins which play a crucial role in antigen presentation. They are among the most polymorphic proteins known, and this polymorphism is thought to be the result of natural selection. To understand the selective pressure acting on the protein and to examine possible differences in the evolutionary dynamics among species, we apply maximum likelihood models of codon substitution to analyze the DRB genes of six mammalian species: human, chimpanzee, macaque, tamarin, dog, and cow. The models account for variable selective pressures across codons in the gene and have the power to detect amino acid residues under either positive or negative selection. Our analysis detected positive selection in the DRB genes in each of the six mammals examined. Comparison with structural data reveals that almost all amino acid residues inferred to be under positive selection in humans are in the peptide binding region (PBR) and are in contact with the antigen side chains, although residues outside of but close to the PBR are also detected. Strong purifying selection is also detected in the PBR, at sites which contact the antigen and at sites which may be involved in dimerization or T cell binding. The analysis demonstrates the utility of the random-sites analysis even when structural information is available. The different mammalian species are found to share many positively or negatively selected sites, suggesting that their functional roles have remained very similar in the different species, despite the different habitats and pathogens of the species.     

Population variation in sexual selection and its effect on size allometry in two dung fly species with contrasting sexual size dimorphism

Body size is one of the most important quantitative traits under evolutionary scrutiny. Sexual size dimorphism (SSD) in a given species is expected to result if opposing selection forces equilibrate differently in both sexes. We document variation in the intensity of sexual and fecundity selection, male and female body size, and thus SSD among 31 and 27 populations of the two dung fly species, Scathophaga stercoraria and Sepsis cynipsea, across Switzerland. Whereas in S. cynipsea females are larger, the SSD is reversed in S. stercoraria. We comprehensively evaluated Fairbairn and Preziosi's (1994) general, three-tiered scenario, hypothesizing that sexual selection for large male size is the major driving force of SSD allometry within these two species. Sexual selection intensity on male size in the yellow dung fly, S. stercoraria, was overall positive, greater, and more variable among populations than fecundity selection on females. Also, sexual selection intensity in a given population correlated positively with mean male body size of that population for both the field-caught fathers and their laboratory-reared sons, indicating a response to selection. In S. cvnipsea, sexual selection intensity on males was lower overall and significantly positive, about equal in magnitude, but more variable than fecundity selection on females. However, there was no correlation between the intensity of sexual selection and mean male body size among populations. In both species, the laboratory-reared offspring indicate genetic differentiation among populations in body size. Despite fulfillment of all key prerequisites, at least in S. stercoraria, we did not find hypoallometry for SSD (Rensch's rule, i.e., greater evolutionary divergence in male size than female size) for the field-caught parents or the laboratory-reared offspring: Female size was isometric to male size in both species. We conclude that S. cynipsea does not fit some major requirements of Fairbairn and Preziosi's (1994) scenario, whereas for S. stercoraria we found partial support for it. Failure to support Rensch's rule within the latter species may be due to phylogenetic or other constraints, power limitations, erroneous estimates of sexual selection, insufficient genetic isolation of populations, or sex differences in viability selection against large size.     

Covariation between predation risk, body size and fin elaboration in the green swordtail, Xiphophorus helleri

Natural and sexual selection can have either opposing or synergistic effects on the evolution of traits. In the green swordtail Xiphophorus helleri , sexual selection arising from female choice is known to favour larger males and males with longer swords. We examined variation in male and female size and fin morphology among 15 populations that varied in their predation environments. Males and females from populations in which piscivorous fishes were present had longer and deeper bodies than did males and females from populations in which piscivorous fishes were absent. Controlling for a positive effect of body size on sword length, males from populations in which piscivores were present had relatively shorter swords than did males from populations in which piscivores were absent. The associations between morphology and predation environment may be due to direct effects of predation, indirect effects of predation, other sources of selection that covary with predator presence, or other environmental effects on trait expression. These results suggest that while sexual selection favours longer swords, natural selection may have an opposing effect on sword length in populations with predators. Natural selection on body size, however, may act synergistically with sexual selection in populations with predators; both may favour the evolution of larger body size. The body size results for X. helleri contrast with related taxa that have become model systems for the study of life history evolution.  © 2004 The Linnean Society of London, Biological Journal of the Linnean Society , 2004, 83 , 87–100.     

The interpretation of selection coefficients

Evolutionary biologists have an array of powerful theoretical techniques that can accurately predict changes in the genetic composition of populations. Changes in gene frequencies and genetic associations between loci can be tracked as they respond to a wide variety of evolutionary forces. However, it is often less clear how to decompose these various forces into components that accurately reflect the underlying biology. Here, we present several issues that arise in the definition and interpretation of selection and selection coefficients, focusing on insights gained through the examination of selection coefficients in multilocus notation. Using this notation, we discuss how its flexibility—which allows different biological units to be identified as targets of selection—is reflected in the interpretation of the coefficients that the notation generates. In many situations, it can be difficult to agree on whether loci can be considered to be under “direct” versus “indirect” selection, or to quantify this selection. We present arguments for what the terms direct and indirect selection might best encompass, considering a range of issues, from viability and sexual selection to kin selection. We show how multilocus notation can discriminate between direct and indirect selection, and describe when it can do so.     

Variability for host preference in insect populations: Mechanistic and evolutionary models

Two models that explain variation in behaviour associated with locating and accepting different habitats (host plants) are described and analyzed. One model describes the dynamics of search-mode ontogeny in Battus philenor butterflies. This model predicts that the proportion of females using either of two search modes at any given time reflects an equilibrium between the rate at which females switch from using a narrow-leaf search mode to using a broad-leaf search mode and the rate at which the opposite switch is made. Preliminary data suggest that the model predicts reasonably well the observed seasonal change in predominant search mode in the field. The second model, really a set of related models, describes the dynamics of genes that influence searching behaviour. Several predictions of these models are: (1) gentic variation for proportional allocation of offspring to different habitats should be more common under soft-selection regimes than under hard-selection regimes. (2) Polyphagy should be more common under soft selection than under hard selection. (3) Whether changes in the relative abundances or relative quality of different habitats lead to evolutionary change in apportionment of offspring to habitats depends in a complex way on mode of population regulation, method of search, type of limitation of fecundity and genetic properties of loci affecting preference. Although the two types of models superficially appear to address different types of behavioural variation, they may be used in a complementary fashion to understand the evolution of habitat selection behaviour.     

蜂桶寨自然保护区小熊猫对生境的选择

2002年4月至11月,在邛崃山系宝兴蜂桶寨自然保护区设点,应用资源选择函数和资源选择指数研究了小熊猫对生境的选择和利用。结果表明,影响小熊猫生境选择的关键因子是水源距离、竹子基径、灌木密度;次关键因子是坡位、树桩密度、倒木密度;次要因子是坡向、乔木密度;而郁闭度、坡度、植被类型、乔木高度、灌木高度、树桩高度、树洞密度、人为干扰的影响不明显。小熊猫喜欢在水源较近(<250m)、竹子长势良好(基径大于4 0mm)、灌木和乔木密度大(大于1 5株 20m2)、树桩和倒木数量多(>1根 400m2)、中上坡位、南坡的针叶林或针阔混交林活动。小熊猫的生境资源选择函数为:logit(P)=-13 527-3 180×水源距离 2 702×竹子基径 2 582×灌木密度 2 134×树桩密度 2 104×坡位 1 622×倒木密度-1 066×坡向 0 934×乔木密度……小熊猫对生境的选择概率为:P=elogit(P) (1 elogit(P))