THE EVOLUTION OF STRONG REPRODUCTIVE ISOLATION

Felsenstein distinguished two ways by which selection can directly strengthen isolation. First, a modifier that strengthens prezygotic isolation can be favored everywhere. This fits with the traditional view of reinforcement as an adaptation to reduce deleterious hybridization by strengthening assortative mating. Second, selection can favor association between different incompatibilities, despite recombination. We generalize this "two allele" model to follow associations among any number of incompatibilities, which may include both assortment and hybrid inviability. Our key argument is that this process, of coupling between incompatibilities, may be quite different from the usual view of reinforcement: strong isolation can evolve through the coupling of any kind of incompatibility, whether prezygotic or postzygotic. Single locus incompatibilities become coupled because associations between them increase the variance in compatibility, which in turn increases mean fitness if there is positive epistasis. Multiple incompatibilities, each maintained by epistasis, can become coupled in the same way. In contrast, a single-locus incompatibility can become coupled with loci that reduce the viability of haploid hybrids because this reduces harmful recombination. We obtain simple approximations for the limits of tight linkage, and strong assortment, and show how assortment alleles can invade through associations with other components of reproductive isolation.     

When is sympatric speciation truly adaptive? An analysis of the joint evolution of resource utilization and assortative mating

The plausibility of sympatric speciation has long been debated among evolutionary ecologists. The process necessarily involves two key elements: the stable coexistence of at least two ecologically distinct types and the emergence of reproductive isolation. Recent theoretical studies within the theoretical framework of adaptive dynamics have shown how both these processes can be driven by natural selection. In the standard scenario, a population first evolves to an evolutionary branching point, next, disruptive selection promotes ecological diversification within the population, and, finally, the fitness disadvantage of intermediate types induces a selection pressure for assortative mating behaviour, which leads to reproductive isolation and full speciation. However, the full speciation process has been mostly studied through computer simulations and only analysed in part. Here I present a complete analysis of the whole speciation process by allowing for the simultaneous evolution of the branching ecological trait as well as a continuous trait controlling mating behaviour. I show how the joint evolution can be understood in terms of a gradient landscape, where the plausibility of different evolutionary paths can be evaluated graphically. I find sympatric speciation unlikely for scenarios with a continuous, unimodal, distribution of resources. Rather, ecological settings where the fitness inferiority of intermediate types is preserved during the ecological branching are more likely to provide opportunity for adaptive, sympatric speciation. Such scenarios include speciation due to predator avoidance or specialization on discrete resources. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

When do host–parasite interactions drive the evolution of non‐random mating?

Interactions with parasites may promote the evolution of disassortative mating in host populations as a mechanism through which genetically diverse offspring can be produced. This possibility has been confirmed through simulation studies and suggested for some empirical systems in which disassortative mating by disease resistance genotype has been documented. The generality of this phenomenon is unclear, however, because existing theory has considered only a subset of possible genetic and mating scenarios. Here we present results from analytical models that consider a broader range of genetic and mating scenarios and allow the evolution of non-random mating in the parasite as well. Our results confirm results of previous simulation studies, demonstrating that coevolutionary interactions with parasites can indeed lead to the evolution of host disassortative mating. However, our results also show that the conditions under which this occurs are significantly more fickle than previously thought, requiring specific forms of infection genetics and modes of non-random mating that do not generate substantial sexual selection. In cases where such conditions are not met, hosts may evolve random or assortative mating. Our analyses also reveal that coevolutionary interactions with hosts cause the evolution of non-random mating in parasites as well. In some cases, particularly those where mating occurs within groups, we find that assortative mating evolves sufficiently to catalyze sympatric speciation in the interacting species.     

Male Ant-mimicking Salticid Spiders Discriminate Between Retreat Silks of Sympatric Females: Implications for Pre-mating Reproductive Isolation

Mate recognition is essential to reproductive success especially under sympatry where encounters between the sexes of different species is likely. We examined the response of male ant-mimicking salticid spiders of the genus Myrmarachne and of five different color forms to retreat and dragline silks of sympatric females of six color forms to determine whether silk-based cues could be used as pre-mating isolation mechanisms and aid species determination. We found evidence for polymorphism within one species Myrmarachne plataleoides, a well-known mimic of the weaver ant Oecophylla smaragdina. Male color morphs of this species showed cross-interest in female silks of other color morphs of this species, but also exhibited greatest preference for the silk of their own color morph, providing evidence for assortative mating and the possibility of silk-based cues as mechanisms of incipient speciation via disruptive selection. Males of two other color forms exhibited unambiguous preference for the silk of their own color forms, suggesting that these two forms are distinct species. The silk-based findings were confirmed by no-choice mating experiments and opportunistic observations of natural matings.     

Environmental influences on hovering behavior ofTabanus nigrovittatus andT. conterminus (Diptera: Tabanidae)

Hovering aggregations of male salt marsh greenheads Tabanus nigrovittatusand the sibling species T. conterminuswere observed on marshes in southern New Jersey. T. nigrovittatusmales hovered over expanses of short marsh grasses, while T. conterminushovered over tidal creeks and near other prominent landmarks. T. nigrovittatusexhibited two distinct daily hovering periods. The timing of these periods varied daily but showed a strong negative correlation with ambient temperature. A principal-components analysis identified a combination of ambient temperature, black-body temperature, and light intensity as most predictive of hovering onset. T. conterminushovered during a time period which was generally intermediate to the two hovering periods of T. nigrovittatus.Temporal partitioning of hovering windows may represent a premating isolating mechanism.     

Effect of assortative mating on genetic change due to selection

Summary Two mathematical models (A and B) were used to study joint effects of selection and assortative mating on genetic change. Computer simulation was used to verify and extend the results. In each model, the genotype was additive with equal effects at each of N loci and the environmental distribution was N(0, ²). In Model A, each locus had two alleles; in Model B, allelic effects at each locus followed a normal distribution. Using Model A, genetic change with assortative or random mating of selected parents was evaluated for combinations of number of loci (N = 1, 2, 3), heritability in base population (H^[0] = 0.2, 0.5, 0.8), allelic frequency in base population (p = 0.1, 0.5), and proportion selected ( = 0.20, 0.85). Using Model B, genetic change with or without assortative mating was calculated for combinations of N (1, 2, 3, 5, 10, 100, H^[0] (0.2, 0.5, 0.8) and (0.20, 0.85). Response to selection under both mating systems in a finite population was estimated using Model A from 200 replications of a computer simulation; this was done for all combinations of N (1,2, 3, 5, 10) and (0.20, 0.85), with H^[0] = 0.5 and p = 0.1. Results obtained with both models indicate that the effect of assortative mating on genetic change increases with H^[0] and , and decreases with p. With Model A, the relationship between N and the effect of assortative mating on genetic change was not clear; with Model B, however, the advantage of assortative over random mating increased with N, as expected. Simulation results were in agreement with theory of Model A. This study indicates that selection with assortative mating can have a sizable (10 to 20%) long-term advantage over selection with random mating of parents when H^[0] is high, p is low and is large.     

An Alternative Approach to Modelling the Assortative Mating Process

In this article we demonstrate how the difficulties encountered from consideration of two-sided assortation for a characteristic (or set of characteristics) in human populations can be overcome. This is achieved, essentially, by postulating a socio-environmental variable (based on an individual's lifetime experiences) over which individuals are mating assortatively. The value an individual has on this scale determines his mean value for the characteristic under consideration. In other words, there is a relationship between the characteristic and the socioenvironmental scale. As well, individuals may be mating assortatively for the characteristic under consideration (although not necessarily). Thus we achieve assortative mating for a single characteristic as a result of mixing, simultaneously, over more than just one variable. Expansions to more ‘mixing’ scales than a single socio-environmental variable are quite straightforward.