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1.
Article in English | MEDLINE | ID: mdl-38316551

ABSTRACT

Speciation often involves the evolution of multiple genetic-based barriers to gene flow (i.e., "coupling"). However, barriers may exhibit a diversity of evolutionary interactions during speciation. These dynamics are important in reinforcement, where selection may favor different prezygotic isolating barriers to avoid maladaptive hybridization. Here we study the interaction between evolution of sexual and habitat isolation. We first review the empirical literature where both barriers were explicitly considered, and then develop a population genetic model of reinforcement. Most studies of both sexual and habitat isolation were found in phytophagous insect systems. In 76% of these studies, both barriers coevolved; the remaining cases either showed only habitat isolation (21%) or only sexual isolation (3%). Our two-allele genetic mechanism model of each barrier also found that these often coevolved, but habitat isolation was generally more effective during reinforcement. Depending on the fitness of hybrids (e.g., Dobzhansky-Muller incompatibilities) and initial migration rate, these barriers could either facilitate, curtail, or have no effect on each other. This indicates that basic parameters will alter the underlying evolutionary dynamics, and thus the nature of "speciation coupling" will be highly variable in natural systems. Finally, we studied initially asymmetrical migration rates and found that populations with higher initial emigration evolved stronger habitat isolation, while populations that initially received more immigrants exhibited stronger sexual isolation. These results are in line with observations in some empirical studies, but more data is needed to test their generality.


Subject(s)
Biological Evolution , Ecosystem , Reproductive Isolation , Animals , Genetic Speciation , Gene Flow , Selection, Genetic , Models, Genetic , Insecta/physiology
2.
Evolution ; 77(2): 496-508, 2023 02 04.
Article in English | MEDLINE | ID: mdl-36626802

ABSTRACT

Theoretical models typically assume that speciation is driven by divergence in female preference functions for secondary sexual traits. However, little is known about how these functions diverge between incipient species. This study used song playback experiments and mate choice tests to characterize female preference functions for divergent male courtship songs between two incipient species of Drosophila athabasca complex; D. athabasca (WN) and Drosophila mahican (EA). The study focused on two male song parameters: pulses per burst (PPB) and inter-pulse interval (IPI). Preference functions for PPB were open-ended and lacked species-specificity. In contrast, preference functions for IPI revealed a closed shape, with peak preferences highly divergent between species. Thus, females imposed divergent and ongoing sexual selection on male IPI. Further work demonstrated variation in peak preferences and choosiness for IPI across genetic lines, while F1 hybrid females varied extensively in their mating preferences across different heterospecific line crosses. Finally, F2 female genotypes with foreign single-copy chromosome substitutions showed little to no change in preferences until three or four chromosomes were combined: indicating strong dominance epistasis. These results suggest "veiled" or hidden segregating female preference alleles for male speciation phenotypes. This may explain the rapid speciation observed in this species complex.


Subject(s)
Drosophila , Mating Preference, Animal , Animals , Male , Female , Drosophila/genetics , Alleles , Epistasis, Genetic , Courtship , Genotype , Sexual Behavior, Animal
3.
Evolution ; 77(1): 318-328, 2023 Jan 23.
Article in English | MEDLINE | ID: mdl-36622661

ABSTRACT

The concept of a "speciation continuum" has gained popularity in recent decades. It emphasizes speciation as a continuous process that may be studied by comparing contemporary population pairs that show differing levels of divergence. In their recent perspective article in Evolution, Stankowski and Ravinet provided a valuable service by formally defining the speciation continuum as a continuum of reproductive isolation, based on opinions gathered from a survey of speciation researchers. While we agree that the speciation continuum has been a useful concept to advance the understanding of the speciation process, some intrinsic limitations exist. Here, we advocate for a multivariate extension, the speciation hypercube, first proposed by Dieckmann et al. in 2004, but rarely used since. We extend the idea of the speciation cube and suggest it has strong conceptual and practical advantages over a one-dimensional model. We illustrate how the speciation hypercube can be used to visualize and compare different speciation trajectories, providing new insights into the processes and mechanisms of speciation. A key strength of the speciation hypercube is that it provides a unifying framework for speciation research, as it allows questions from apparently disparate subfields to be addressed in a single conceptual model.


Subject(s)
Genetic Speciation , Reproductive Isolation
4.
J Evol Biol ; 36(2): 355-367, 2023 02.
Article in English | MEDLINE | ID: mdl-36576691

ABSTRACT

Speciation and sexual isolation often occur when divergent female mating preferences target male secondary sexual traits. Despite the importance of such male signals, little is known about their evolvability and genetic linkage to other traits during speciation. To answer these questions, we imposed divergent artificial selection for 10 non-overlapping generations on the Inter-Pulse-Interval (IPI) of male courtship songs; which has been previously shown to be a major species recognition trait for females in the Drosophila athabasca species complex. Focusing on one of the species, Drosophila mahican (previously known as EA race), we examined IPI's: (1) rate of divergence, (2) response to selection in different directions, (3) genetic architecture of divergence and (4) by-product effects on other traits that have diverged in the species complex. We found rapid and consistent response for higher IPI but less response to lower IPI; implying asymmetrical constraints. Genetic divergence in IPI differed from natural species in X versus autosome contribution and in dominance, suggesting that evolution may take different paths. Finally, selection on IPI did not alter other components of male songs, or other ecological traits, and did not cause divergence in female preferences, as evidenced by lack of sexual isolation. This suggests that divergence of male courtship song IPI is unconstrained by genetic linkage with other traits in this system. This lack of linkage between male signals and other traits implies that female preferences or ecological selection can co-opt and mould specific male signals for species recognition free of genetic constraints from other traits.


Subject(s)
Drosophila , Mating Preference, Animal , Animals , Male , Female , Phenotype , Drosophila/genetics , Reproduction , Genetic Linkage , Sexual Behavior, Animal , Genetic Speciation
5.
J Evol Biol ; 35(8): 1045-1059, 2022 08.
Article in English | MEDLINE | ID: mdl-35830473

ABSTRACT

The role of sexual selection in speciation is implicated in both empirical case studies and larger comparative works. However, sexual selection faces two major problems in driving speciation. First, because females with novel preferences search for their initially rare males, search costs are expected to curtail initial sexual divergence. Second, if these populations come back into sympatry, sexual divergence may be erased due to hybridization. A major goal is to understand which conditions increase the likelihood of overcoming these problems. Here we generated a diploid population genetic model of how female search costs and evolution of female 'choosiness' (i.e. preference strength) interact to drive speciation in allopatry and secondary contact. We studied the model using numerical simulations in the context of two different male traits, ecologically 'arbitrary' versus 'magic' traits. First, in allopatry, without female search costs only minor and fluctuating sexual isolation evolved. In contrast, with female search costs, sexual isolation was highly curtailed with arbitrary male traits but was greatly facilitated with magic traits. However, because search costs selected for reduced choosiness, sexual isolation with magic traits was eventually eroded, the rate determined by the genetic architecture of choosiness. These factors also played a key role in secondary contact; with evolvable choosiness and female search costs, pure sexual selection models collapsed upon secondary contact. However, when we added selection against hybrids (i.e. reinforcement) to this model, we found that speciation could be maintained under a wide range of conditions with arbitrary male traits, but not with magic male traits. This surprisingly suggests that arbitrary male traits are in some cases more likely to aid speciation than magic male traits. We discuss these findings and relate them to empirical literature on female choosiness within species and in hybrids.


Subject(s)
Mating Preference, Animal , Animals , Female , Genetic Speciation , Hybridization, Genetic , Male , Phenotype , Selection, Genetic , Sexual Selection , Sympatry
6.
Am Nat ; 197(6): 690-707, 2021 06.
Article in English | MEDLINE | ID: mdl-33989143

ABSTRACT

AbstractMale secondary sexual traits are one of the most striking and diverse features of the animal kingdom. While these traits are often thought to evolve via sexual selection, many questions remain about their patterns of diversification and their role in speciation. To address these questions, I performed a comparative study of precopulatory male courtship songs of 119 Drosophila species across 10 distinct species groups. I related song divergence to genetic distances, geographic relationships, and sexual isolation between species. On the basis of pairwise Euclidean song distances, species groups typically retained their phylogenetic signal while species within groups diverged five times more in sympatry relative to allopatry, producing a pattern of reproductive character displacement. This occurred despite similar genetic distances in allopatry and sympatry, was exaggerated among younger species pairs, and was driven primarily by the parameter interpulse interval. While sexual isolation in sympatry was high even with low song divergence, these variables were correlated with each other and with increased divergence of female mating preferences in sympatry. The widespread pattern of character displacement implies that allopatric divergence due to processes like sexual selection are very slow relative to sympatric processes such as reinforcement and reproductive interference in driving song diversification across Drosophila.


Subject(s)
Drosophila , Sexual Behavior, Animal , Vocalization, Animal , Animals , Drosophila/physiology , Female , Male , Mating Preference, Animal/physiology , Phylogeny , Sexual Behavior, Animal/physiology , Sympatry , Vocalization, Animal/physiology
7.
Evolution ; 73(9): 1759-1773, 2019 09.
Article in English | MEDLINE | ID: mdl-31077339

ABSTRACT

The relative importance of male and female mating preferences in causing sexual isolation between species remains a major unresolved question in speciation. Despite previous work showing that male courtship bias and/or female copulation bias for conspecifics occur in many taxa, the present study is one of the first large-scale works to study their relative divergence. To achieve this, we used data from the literature and present experiments across 66 Drosophila species pairs. Our results revealed that male and female mate preferences are both ubiquitous in Drosophila but evolved largely independently, suggesting different underlying evolutionary and genetic mechanisms. Moreover, their relative divergence strongly depends on the geographical relationship of species. Between allopatric species, male courtship and female copulation preferences diverged at very similar rates, evolving approximately linearly with time of divergence. In sharp contrast, between sympatric species pairs, female preferences diverged much more rapidly than male preferences and were the only drivers of enhanced sexual isolation in sympatry and Reproductive Character Displacement (RCD). Not only does this result suggest that females are primarily responsible for such processes as reinforcement, but it also implies that evolved female preferences may reduce selection for further divergence of male courtship preferences in sympatry.


Subject(s)
Drosophila melanogaster/genetics , Genetic Speciation , Mating Preference, Animal , Sexual Behavior, Animal , Sympatry , Animals , Computer Simulation , Female , Geography , Male , Phylogeny , Reproduction , Reproductive Isolation , Sex Factors
8.
Ecol Evol ; 8(5): 2852-2867, 2018 03.
Article in English | MEDLINE | ID: mdl-29531700

ABSTRACT

The rapid evolution of sexual isolation in sympatry has long been associated with reinforcement (i.e., selection to avoid maladaptive hybridization). However, there are many species pairs in sympatry that have evolved rapid sexual isolation without known costs to hybridization. A major unresolved question is what evolutionary processes are involved in driving rapid speciation in such cases. Here, we focus on one such system; the Drosophila athabasca species complex, which is composed of three partially sympatric and interfertile semispecies: WN, EA, and EB. To study speciation in this species complex, we assayed sexual and genomic isolation within and between these semispecies in both sympatric and allopatric populations. First, we found no evidence of reproductive character displacement (RCD) in sympatric zones compared to distant allopatry. Instead, semispecies were virtually completely sexually isolated from each other across their entire ranges. Moreover, using spatial approaches and coalescent demographic simulations, we detected either zero or only weak heterospecific gene flow in sympatry. In contrast, within each semispecies we found only random mating and little population genetic structure, except between highly geographically distant populations. Finally, we determined that speciation in this system is at least an order of magnitude older than previously assumed, with WN diverging first, around 200K years ago, and EA and EB diverging 100K years ago. In total, these results suggest that these semispecies should be given full species status and we adopt new nomenclature: WN-D. athabasca, EA-D. mahican, and EB-D. lenape. While the lack of RCD in sympatry and interfertility do not support reinforcement, we discuss what additional evidence is needed to further decipher the mechanisms that caused rapid speciation in this species complex.

9.
Curr Zool ; 63(2): 195-203, 2017 Apr.
Article in English | MEDLINE | ID: mdl-29491977

ABSTRACT

Anthropogenic pollutants have the potential to disrupt reproductive strategies. Little is known about how lead (Pb2+) exposure disrupts individual-level responses in reproductive behaviors, which are important for fitness. Drosophila melanogaster was used as a model system to determine the effects of: 1) developmental lead exposure on pre-mating reproductive behaviors (i.e., mate preference), and 2) lead exposure and mating preferences on fitness in the F0 parental generation and F1 un-exposed offspring. Wild-type strains of D. melanogaster were reared from egg stage to adulthood in control or leaded medium (250 µM PbAc) and tested for differences in: mate preference, male song performance, sex pheromone expression, fecundity, mortality, and body weight. F0 leaded females preferentially mated with leaded males (i.e., asymmetrical positive assortative mating) in 2-choice tests. This positive assortative mating was mediated by the females (and not the males) and was dependent upon context and developmental exposure to Pb. Neither the courtship song nor the sex pheromone profile expressed by control and leaded males mediated the positive assortative mating in leaded females. Leaded females did not incur a fitness cost in terms of reduced fecundity, increased mortality, or decreased body weight by mating with leaded males. These results suggest that sublethal exposure to lead during development can alter mate preferences in adults, but not fitness measures once lead exposure has been removed. We suggest that changes in mate preference may induce fitness costs, as well as long-term population and multi-generational implications, if pollution is persistent in the environment.

10.
Evolution ; 70(3): 526-42, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26831347

ABSTRACT

Understanding speciation requires the identification of traits that cause reproductive isolation. This remains a major challenge since it is difficult to determine which of the many divergent traits actually caused speciation. To overcome this difficulty, we studied the sexual cue traits and behaviors associated with rapid speciation between EA and WN sympatric behavioral races of Drosophila athabasca that diverged only 16,000-20,000 years ago. First, we found that sexual isolation was essentially complete and driven primarily by divergent female mating preferences. To determine the target of female mate choice, we found that, unlike cuticular hydrocarbons (CHCs), male courtship song is highly divergent between EA and WN in both allopatry and sympatry and is not affected by latitudinal variation. We then used pheromone rub-off experiments to show no effect of CHCs on divergent female mate choice. In contrast, both male song differences and male mating success in hybrids exhibited a large X-effect and playback song experiments confirmed that male courtship song is indeed the target of sexual isolation. These results show that a single secondary sexual trait is a major driver of speciation and suggest that we may be overestimating the number of traits involved in speciation when we study older taxa.


Subject(s)
Drosophila/classification , Drosophila/genetics , Genetic Speciation , Mating Preference, Animal , Animals , Courtship , Drosophila/physiology , Female , Male , Pheromones/metabolism , Reproductive Isolation , United States , Vocalization, Animal
11.
Curr Zool ; 62(2): 155-167, 2016 Apr.
Article in English | MEDLINE | ID: mdl-29491903

ABSTRACT

When partially reproductively isolated species come back into secondary contact, these taxa may diverge in mating preferences and sexual cues to avoid maladaptive hybridization, a process known as reinforcement. This phenomenon often leads to reproductive character displacement (RCD) between sympatric and allopatric populations of reinforcing species that differ in their exposure to hybridization. Recent discussions have reinvigorated the idea that RCD may give rise to additional speciation between conspecific sympatric and allopatric populations, dubbing the concept "cascade reinforcement." Despite some empirical studies supporting cascade reinforcement, we still know very little about the conditions for its evolution. In the present article, we address this question by developing an individual-based population genetic model that explicitly simulates cascade reinforcement when one of the hybridizing species is split into sympatric and allopatric populations. Our results show that when sympatric and allopatric populations reside in the same environment and only differ in their exposure to maladaptive hybridization, migration between them generally inhibits the evolution of cascade by spreading the reinforcement alleles from sympatry into allopatry and erasing RCD. Under these conditions, cascade reinforcement only evolved when migration rate between sympatric and allopatric populations was very low. This indicates that stabilizing sexual selection in allopatry is generally ineffective in preventing the spread of reinforcement alleles. Only when sympatric and allopatric populations experienced divergent ecological selection did cascade reinforcement evolve in the presence of substantial migration. These predictions clarify the conditions for cascade reinforcement and facilitate our understanding of existing cases in nature.

12.
Evolution ; 68(4): 1150-62, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24274675

ABSTRACT

Among the most debated subjects in speciation is the question of its mode. Although allopatric (geographical) speciation is assumed the null model, the importance of parapatric and sympatric speciation is extremely difficult to assess and remains controversial. Here I develop a novel approach to distinguish these modes of speciation by studying the evolution of reproductive isolation (RI) among taxa. I focus on the Drosophila genus, for which measures of RI are known. First, I incorporate RI into age-range correlations. Plots show that almost all cases of weak RI are between allopatric taxa whereas sympatric taxa have strong RI. This either implies that most reproductive isolation (RI) was initiated in allopatry or that RI evolves too rapidly in sympatry to be captured at incipient stages. To distinguish between these explanations, I develop a new "rate test of speciation" that estimates the likelihood of non-allopatric speciation given the distribution of RI rates in allopatry versus sympatry. Most sympatric taxa were found to have likely initiated RI in allopatry. However, two putative candidate species pairs for non-allopatric speciation were identified (5% of known Drosophila). In total, this study shows how using RI measures can greatly inform us about the geographical mode of speciation in nature.


Subject(s)
Drosophila/genetics , Reproductive Isolation , Animal Distribution , Animals , Genetic Speciation , Geography , Sympatry
13.
Evolution ; 67(6): 1805-14, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23730771

ABSTRACT

Understanding the evolutionary mechanisms that facilitate speciation and explain global patterns of species diversity has remained a challenge for decades. The most general pattern of species biodiversity is the latitudinal gradient, whereby species richness increases toward the tropics. Although such a global pattern probably has a multitude of causes, recent attention has focused on the hypothesis that speciation and the evolution of reproductive isolation occur faster in the tropics. Here, I tested this prediction using a dataset on premating and postzygotic isolation between recently diverged Drosophila species. Results showed that while the evolution of premating isolation was not greater between tropical Drosophila relative to nontropical species, postzygotic isolation evolved faster in the tropics. In particular, hybrid male sterility was much greater among tropical Drosophila compared to nontropical species pairs of similar genetic age. Several testable explanations for the novel pattern are discussed, including greater role for sterility-inducing bacterial endosymbionts in the tropics and more intense sperm-sperm competition or sperm-egg sexual conflict in the tropics. The results imply that processes of speciation in the tropics may evolve at different rates or may even be somewhat different from those at higher latitudes.


Subject(s)
Drosophila/genetics , Evolution, Molecular , Infertility, Male/genetics , Tropical Climate , Animals , Genetic Speciation , Hybridization, Genetic , Male , Reproductive Isolation , Time Factors
14.
PLoS Genet ; 8(6): e1002795, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22761593

ABSTRACT

The extent and nature of genetic incompatibilities between incipient races and sibling species is of fundamental importance to our view of speciation. However, with the exception of hybrid inviability and sterility factors, little is known about the extent of other, more subtle genetic incompatibilities between incipient species. Here we experimentally demonstrate the prevalence of such genetic incompatibilities between two young allopatric sibling species, Drosophila simulans and D. sechellia. Our experiments took advantage of 12 introgression lines that carried random introgressed D. sechellia segments in different parts of the D. simulans genome. First, we found that these introgression lines did not show any measurable sterility or inviability effects. To study if these sechellia introgressions in a simulans background contained other fitness consequences, we competed and genetically tracked the marked alleles within each introgression against the wild-type alleles for 20 generations. Strikingly, all marked D. sechellia introgression alleles rapidly decreased in frequency in only 6 to 7 generations. We then developed computer simulations to model our competition results. These simulations indicated that selection against D. sechellia introgression alleles was high (average s = 0.43) and that the marker alleles and the incompatible alleles did not separate in 78% of the introgressions. The latter result likely implies that most introgressions contain multiple genetic incompatibilities. Thus, this study reveals that, even at early stages of speciation, many parts of the genome diverge to a point where introducing foreign elements has detrimental fitness consequences, but which cannot be seen using standard sterility and inviability assays.


Subject(s)
Drosophila/genetics , Genetic Speciation , Hybridization, Genetic/genetics , Reproductive Isolation , Alleles , Animals , Chromosome Mapping , Genetic Fitness , Genome, Insect , Infertility/genetics , Selection, Genetic , Species Specificity
15.
Evolution ; 66(5): 1430-46, 2012 May.
Article in English | MEDLINE | ID: mdl-22519782

ABSTRACT

Understanding how often natural selection directly favors speciation, a process known as reinforcement, has remained an outstanding problem for over 70 years. Although reinforcement has been strongly criticized in the past, it is once again seen as more realistic due to the seminal discovery of enhanced prezygotic isolation among sympatric species and to a handful of well-studied examples. Nevertheless, the pattern of enhanced isolation in sympatry has alternative explanations, highlighting the need to uncover unique signatures of reinforcement to determine its overall frequency in nature. Using a novel dataset on asymmetrical prezygotic and postzygotic isolation among Drosophila species, I uncover new patterns explicitly predicted by reinforcement. Broadly, I found that almost all sympatric species had concordant isolation asymmetries, where the more costly reciprocal mating has greater prezygotic isolation relative to the less costly mating. No such patterns exist in allopatry. Using simulations, I ruled out alternative explanations and showed that concordant isolation asymmetries in sympatry are likely unique signatures of reinforcement. These results allowed me to estimate that reinforcement may impact 60-83% of all sympatric Drosophila and enhance premating isolation by 18-26%. These findings suggest that reinforcement plays a key role in Drosophila speciation.


Subject(s)
Drosophila/genetics , Genetic Speciation , Reproductive Isolation , Sympatry , Animals , Drosophila/classification , Drosophila/physiology , Female , Hybridization, Genetic , Mating Preference, Animal , Models, Biological , Phylogeography , Reproduction , Selection, Genetic , Sex Ratio
16.
Genetics ; 186(1): 219-39, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20551441

ABSTRACT

Genomic tools and analyses are now being widely used to understand genome-wide patterns and processes associated with speciation and adaptation. In this article, we apply a genomics approach to the model organism Drosophila melanogaster. This species originated in Africa and subsequently spread and adapted to temperate environments of Eurasia and the New World, leading some populations to evolve reproductive isolation, especially between cosmopolitan and Zimbabwean populations. We used tiling arrays to identify highly differentiated regions within and between North America (the United States and Caribbean) and Africa (Cameroon and Zimbabwe) across 63% of the D. melanogaster genome and then sequenced representative fragments to study their genetic divergence. Consistent with previous findings, our results showed that most differentiation was between populations living in Africa vs. outside of Africa (i.e., "out-of-Africa" divergence), with all other geographic differences being less substantial (e.g., between cosmopolitan and Zimbabwean races). The X chromosome was much more strongly differentiated than the autosomes between North American and African populations (i.e., greater X divergence). Overall differentiation was positively associated with recombination rates across chromosomes, with a sharp reduction in regions near centromeres. Fragments surrounding these high F(ST) sites showed reduced haplotype diversity and increased frequency of rare and derived alleles in North American populations compared to African populations. Nevertheless, despite sharp deviation from neutrality in North American strains, a small set of bottleneck/expansion demographic models was consistent with patterns of variation at the majority of our high F(ST) fragments. Although North American populations were more genetically variable compared to Europe, our simulation results were generally consistent with those previously based on European samples. These findings support the hypothesis that most differentiation between North America and Africa was likely driven by the sorting of African standing genetic variation into the New World via Europe. Finally, a few exceptional loci were identified, highlighting the need to use an appropriate demographic null model to identify possible cases of selective sweeps in species with complex demographic histories.


Subject(s)
Drosophila melanogaster/genetics , Genetic Variation , Genome, Insect/genetics , Genomics , Africa , Analysis of Variance , Animals , Female , Male , North America , Sequence Analysis, DNA
17.
Evolution ; 62(11): 2807-28, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18752599

ABSTRACT

Understanding incipient sexual isolation and speciation is an important pursuit in evolutionary biology. The fruit fly Drosophila melanogaster is a useful model to address questions about the early stages of sexual isolation occurring within widespread species. This species exhibits sexual isolation between cosmopolitan and African flies, especially from Zimbabwe populations. In addition, we have recently described another example of partial sexual isolation between some US and Caribbean populations. This and other phenotypic data suggest that Caribbean flies might be segregating African traits. In the present work we study the geographical variation at the pheromone locus desaturase-2, as well as morphology and courtship behavior across the US-Caribbean region. We find that US and Caribbean populations show sharp geographical clines in all traits and demonstrate that Caribbean traits are more similar to those of Africa than to US populations. Further, African traits in the Caribbean are associated with sexual isolation and best explain variation in sexual isolation when all traits are considered together. These results imply that Caribbean mating preferences are likely to be based on African traits and that even at such early stages of sexual isolation, individuals may already cue in on several traits simultaneously during mate choice.


Subject(s)
Drosophila melanogaster/physiology , Pheromones/physiology , Sexual Behavior, Animal/physiology , Social Isolation/psychology , Africa , Animals , Caribbean Region , Choice Behavior , Drosophila Proteins/genetics , Ecosystem , Fatty Acid Desaturases/genetics , Female , Genetic Variation , Geography , Male , Sex Characteristics
18.
Evolution ; 62(9): 2215-35, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18564374

ABSTRACT

Gene networks are likely to govern most traits in nature. Mutations at these genes often show functional epistatic interactions that lead to complex genetic architectures and variable fitness effects in different genetic backgrounds. Understanding how epistatic genetic systems evolve in nature remains one of the great challenges in evolutionary biology. Here we combine an analytical framework with individual-based simulations to generate novel predictions about long-term adaptation of epistatic networks. We find that relative to traits governed by independently evolving genes, adaptation with epistatic gene networks is often characterized by longer waiting times to selective sweeps, lower standing genetic variation, and larger fitness effects of adaptive mutations. This may cause epistatic networks to either adapt more slowly or more quickly relative to a nonepistatic system. Interestingly, epistatic networks may adapt faster even when epistatic effects of mutations are on average deleterious. Further, we study the evolution of epistatic properties of adaptive mutations in gene networks. Our results show that adaptive mutations with small fitness effects typically evolve positive synergistic interactions, whereas adaptive mutations with large fitness effects evolve positive synergistic and negative antagonistic interactions at approximately equal frequencies. These results provide testable predictions for adaptation of traits governed by epistatic networks and the evolution of epistasis within networks.


Subject(s)
Adaptation, Biological , Epistasis, Genetic , Evolution, Molecular , Gene Regulatory Networks , Models, Genetic , Alleles , Computer Simulation , Genetic Variation , Mutation , Selection, Genetic , Time Factors
19.
Evolution ; 62(8): 2112-21, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18489717

ABSTRACT

Understanding the biological conditions and the genetic basis of early stages of sexual isolation and speciation is an outstanding question in evolutionary biology. It is unclear how much genetic and phenotypic variation for mating preferences and their phenotypic cues is segregating within widespread and human-commensal species in nature. A recent case of incipient sexual isolation between Zimbabwe and cosmopolitan populations of the human-commensal fruit fly Drosophila melanogaster indicates that such species may initiate the process of sexual isolation. However, it is still unknown whether other geographical populations have undergone evolution of mating preferences. In this study we present new data on multiple-choice mating tests revealing partial sexual isolation between the United States and Caribbean populations. We relate our findings to African populations, showing that Caribbean flies are partially sexually isolated from Zimbabwe flies, but mate randomly with West African flies, which also show partial sexual isolation from the United States and Zimbabwe flies. Thus, Caribbean and West African populations seem to exhibit distinct mating preferences relative to populations in the United States and in Zimbabwe. These results suggest that widespread and human-commensal species may harbor different types of mating preferences across their geographical ranges.


Subject(s)
Biological Evolution , Drosophila melanogaster/genetics , Sexual Behavior, Animal , Animals , Bahamas , Crosses, Genetic , Drosophila Proteins/genetics , Female , Genetic Variation , Male , Models, Biological , Models, Genetic , Phenotype , United States
20.
Am Nat ; 167(5): 638-54, 2006 May.
Article in English | MEDLINE | ID: mdl-16671009

ABSTRACT

Most studies of reinforcement speciation focus on the evolution of assortative mating, but R. A. Fisher argued that migration modification is likely to be a common alternative mechanism. Despite previous models showing that assortative mating and migration modification may both be involved in reinforcement, no one has determined their relative evolutionary importance. This is surprising because understanding the biological conditions favoring these mechanisms may explain why certain pairs of species exhibit abutting, nonoverlapping geographical ranges with habitat fidelity while other pairs coexist in sympatry with sexual isolation. In this article, we explicitly model the evolution of both mechanisms simultaneously. First, we explore how these mechanisms differ in their evolutionary dynamics. Second, we ask how they affect each other's evolution and whether the interaction alters their relative importance in reinforcement. Our results reveal that assortative mating may evolve faster and under a broader range of biological conditions than migration modification. However, direct evolutionary interactions favor migration modification when populations experience strong divergent selection. Depending on the nature of postmating isolation, these mechanisms may either interfere with each other's evolution or coevolve in the same system. These results illustrate the importance of studying multiple mechanisms of speciation simultaneously in future speciation models.


Subject(s)
Animal Migration , Biological Evolution , Genetic Speciation , Models, Biological , Sexual Behavior, Animal/physiology , Animals , Computer Simulation , Geography , Hybridization, Genetic , Species Specificity
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