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This study examines within- and cross-country trends and differences in marital sorting by education in Europe. Unlike previous research on assortative mating, our study focuses on the outcomes of the partner search process. We investigate how variations in (a) structural opportunities (educational composition of potential partners) and (b) assortative mating (non-random matching by education) have shaped trends and differences in educational sorting outcomes. Using vital statistics data on all marriages contracted from 2000 to 2020 in Sweden, the Czech Republic, and Italy, we decompose trends and differences in educational sorting outcomes into these two components. Within countries, trends in educational homogamy and hypogamy have been stable or increasing while hypergamy has declined. However, the drivers of these trends varied across countries. For example, in Sweden, shifts in assortative mating and structural opportunities led to more marriages between equally educated spouses, while in Italy, the rise in homogamy stems solely from changes in assortative mating. Within each year, homogamy and heterogamy levels varied between countries. Our findings demonstrate that these cross-country differences can be primarily attributed to variations in assortative mating rather than in opportunity structures. This study adds to recent research studying the structural causes of trends in sorting outcomes. [ABSTRACT FROM AUTHOR]

Increased gender equality in the labor market and the home are both cited as stabilizers to income inequality between households, but shifts in the economic organization of families over the life course instead appear to amplify household income inequality. Using the case of Sweden, where men have taken longer parental leave in recent years and the age at parenthood continues to advance, we analyze between‐family income inequality for couples with a young child. Based on income data from population registers, we decompose how changes in family dynamics, pre‐ and postparenthood, contributed to income inequality in families with children between the years 1995 and 2018. Analyses show no evidence that assortative mating has increased and that a minor decline in inequality between couples over this 24‐year period resulted from two opposing trends: Dis‐equalizing changes related to women's postbirth income advancements were eclipsed by equalizing changes related to the postponement of parenthood. Postbirth income trends reveal how between‐family inequality increased through women's income development and decreased through men's. Our findings confirm the importance of family processes to household inequality and show the complex effects of both changes in the timing of parenthood and improved gender equality. [ABSTRACT FROM AUTHOR]

How colour polymorphisms are maintained in natural populations constitutes a key subject of study for evolutionary ecologists. One of the mechanisms that has been put forward to explain this phenomenon is negative frequency-dependent selection, which can be caused by different mechanisms. Among these mechanisms is mate choice, or the selection as a potential mate of the rare or dissimilar colour morph by the choosy sex of a given species. In the context of colour polymorphism, mate choice predicts the occurrence of a negative assortative mating pattern, whereby different colour morphs mate more often than expected by chance alone. However, negative assortative mating can also result from other mechanisms, making it, at best, a fallible indicator of a mate choice-driven negative frequency-dependent selection. For this reason, experimental evidence explicitly connecting such a mating pattern to mate choice is necessary to claim that a particular colour polymorphism is being maintained by negative frequency-dependent selection. Here we present experimental evidence backing this relationship for the colour polymorphic marine gastropod Littorina saxatilis from the Ría de Vigo (NW Iberian Peninsula), although how specifically these organisms choose their mates remains unclear. This calls for further experimental efforts to clarify this issue and its relationship to the maintenance of colour polymorphism in L. saxatilis. [ABSTRACT FROM AUTHOR]

Sexual selection plays a crucial role in modern evolutionary theory, offering valuable insight into evolutionary patterns and species diversity. Recently, a comprehensive definition of sexual selection has been proposed, defining it as any selection that arises from fitness differences associated with nonrandom success in the competition for access to gametes for fertilization. Previous research on discrete traits demonstrated that non-random mating can be effectively quantified using Jeffreys (or symmetrized Kullback-Leibler) divergence, capturing information acquired through mating influenced by mutual mating propensities instead of random occurrences. This novel theoretical framework allows for detecting and assessing the strength of sexual selection and assortative mating. In this study, we aim to achieve two primary objectives. Firstly, we demonstrate the seamless alignment of the previous theoretical development, rooted in information theory and mutual mating propensity, with the aforementioned definition of sexual selection. Secondly, we extend the theory to encompass quantitative traits. Our findings reveal that sexual selection and assortative mating can be quantified effectively for quantitative traits by measuring the information gain relative to the random mating pattern. The connection of the information indices of sexual selection with the classical measures of sexual selection is established. Additionally, if mating traits are normally distributed, the measure capturing the underlying information of assortative mating is a function of the square of the correlation coefficient, taking values within the non-negative real number set [0, +∞). It is worth noting that the same divergence measure captures information acquired through mating for both discrete and quantitative traits. This is interesting as it provides a common context and can help simplify the study of sexual selection patterns. [ABSTRACT FROM AUTHOR]

How sticky is wealth inequality across generations due to marital sorting? To analyze this question, we utilize a comprehensive Swiss dataset. Our findings highlight that marital sorting based on wealth is especially pronounced at the extremes of the wealth distribution, exacerbating wealth inequality. Simultaneously, we observe that the similarity in wealth between the parents of married partners is substantially less pronounced. Our findings suggest a more significant occurrence of marriages into "new money" than "old money". Consequently, our study shows that parental wealth has a limited role in contributing to the inequality stemming from marital choices. We present evidence that intergenerational social mobility plays a pivotal role in counteracting the potential intensification of wealth structures due to marriage. [ABSTRACT FROM AUTHOR]

Context: Cultural divergence refers to changes over time in behavioural traits. These cultural changes could have important implications for conservation planning, and impact the success of conservation efforts such as translocations. Aims: Here, we investigate the extent, and potential impacts, of cultural divergence in two isolated populations of the Floreana mockingbird (Mimus trifasciatus) on the Galápagos Islands. Methods: Using contemporary recordings of vocalisations we test for spatial vocal differentiation between mockingbird populations. Furthermore, we explore the potential drivers of change using morphological measurements and historical recordings of the species. Key results: We found evidence of spatial and temporal differentiation in vocalisations between the two populations of the Floreana mockingbird. We accurately classified over 75% of the birds to the correct populations based on multivariate measures of audio recordings using canonical analysis of principal coordinates (CAP). We also found significant differences in morphometrics between populations; specifically, beak depth was associated with frequency modulation, an acoustic measure that is significantly different between populations. Furthermore, we found evidence of change in the complexity of the vocalisations over a period of 57 years. Conclusions: Cultural divergence was found in the two remaining populations of this endangered species. Factors such as changes in morphology and cultural drift might have been influenced the change in vocalisation across time and populations. Implications: We highlight the importance of considering behavioural factors when planning reintroductions of endangered species where there is a need to minimise the risk of assortative mating so as to maximise genetic diversity. Cultural changes could have important implications for conservation planning, and impact the success of conservation efforts. We studied the cultural divergence between the last remaining population of the Floreana mockingbird. Anticipating potential challenges caused by cultural divergence will increase the likelihood of success of the species reintroduction to Floreana Island on the Galápagos Islands. [ABSTRACT FROM AUTHOR]

Background: According to the most recent U.S. CDC surveillance data, the rise in prevalence of childhood autism spectrum disorder among minority children has begun to outpace that of non-Hispanic white children. Since prior research has identified possible differences in the extent of mate selection for autistic traits across families of different ethnicity, this study examined variation in autism related traits in contemporaneous, epidemiologically ascertained samples of spousal pairs representing Hispanic and non-Hispanic white populations. The purpose was to determine whether discrepancies by ethnicity could contribute to differential increases in prevalence in the current generation of young children. Methods: Birth records were used to identify all twin pairs born between 2011 and 2013 in California and Missouri. Families were selected at random from pools of English-speaking Hispanic families in California and Non-Hispanic White families in Missouri. Autistic trait data of parents was obtained using the Adult Report Form of the Social Responsiveness Scale (SRS-2). Results: We did not identify a statistically significant difference in the degree of mate selection for autism related traits between Hispanic and non-Hispanic white spousal pairs. However, the degree of spousal correlation observed in this recent cohort was pronounced (on the order of ICC 0.45) and exceeded that typically reported in prior research (on the order of 0.30), surpassing also widely reported estimates for sibling correlation (also on the order of 0.30). Limitations: The sample did not allow for a direct appraisal of change in the magnitude of spousal correlation over time and the ascertainments of trait burden were derived from spouse report. Conclusion: Across two epidemiologically ascertained samples of spousal pairs representing Hispanic and non-Hispanic white families across two U.S. states (respectively, California and Missouri), the extent of autism-related trait co-variation for parents of the current generation of young children is substantial and exceeds correlations typically observed for siblings. Given the heritability of these traits and their relation to autism risk, societal trends in the degree of mate selection for these traits should be considered as possible contributors to subtle increases in the incidence of autism over time and across generations. [ABSTRACT FROM AUTHOR]

The fixation index, FIS, has been a staple measure to detect selection, or departures from random mating in populations. However, current Next Generation Sequencing (NGS) cannot easily estimate FIS, in multi‐locus gene families that contain multiple loci having similar or identical arrays of variant sequences of ≥1 kilobase (kb), which differ at multiple positions. In these families, high‐quality short‐read NGS data typically identify variants, but not the genomic location, which is required to calculate FIS (based on locus‐specific observed and expected heterozygosity). Thus, to assess assortative mating, or selection on heterozygotes, from NGS of multi‐locus gene families, we need a method that does not require knowledge of which variants are alleles at which locus in the genome. We developed such a method. Like FIS, our novel measure, 1HIS, is based on the principle that positive assortative mating, or selection against heterozygotes, and some other processes reduce within‐individual variability relative to the population. We demonstrate high accuracy of 1HIS on a wide range of simulated scenarios and two datasets from natural populations of penguins and dolphins. 1HIS is important because multi‐locus gene families are often involved in assortative mating or selection on heterozygotes. 1HIS is particularly useful for multi‐locus gene families, such as toll‐like receptors, the major histocompatibility complex in animals, homeobox genes in fungi and self‐incompatibility genes in plants. [ABSTRACT FROM AUTHOR]

Background: To date, the magnitude of association and the quality of evidence for cognitive decline (mild cognitive impairment, Alzheimer's disease, and dementia) in couples and risk factors for outcomes have not been reviewed and analyzed systematically. Objective: The aim of this study was to investigate the concordance of cognitive impairment in unrelated spouses and to qualitatively describe potential risk factors. Methods: Eight databases were searched from inception to October 20, 2023. Eligible studies were independently screened and assessed for quality. Statistical analysis was conducted using Stata 15.1 software. The study was preregistered with PROSPERO (CRD42023488024). Results: Eleven studies involving couples were included, with moderate to high evidence quality. Compared to controls, spouses of individuals with cognitive impairment had lower cognitive scores (Cohen's d: 0.18-0.62) and higher risk of cognitive decline (OR = 1.42, 95% CI: 1.15–1.76). The consistency of cognitive impairment between spouses was attributed to three theories: 1) the impact of caregiving stress experienced by the spouse; 2) assortative mating, which suggests that individuals select partners with similar characteristics; and 3) the influence of shared living environments and lifestyles. Conclusions: The cognitive status of one spouse can affect the cognitive function of the other spouse. It is important to consider shared lifestyle, environmental, and psychobehavioral factors, as they may contribute to the risk of cognitive decline by couples. Identifying these factors can inform the development of targeted recommendations for interventions and preventive measures. [ABSTRACT FROM AUTHOR]

The worldwide expansion of female educational opportunities in recent decades has prompted demographers to assess the frequency with which women marry up (hypergamy) or down (hypogamy) with regard to education. A series of articles documented dramatic and nearly universal declines in hypergamy over time and across female educational advantage. However, this previous work investigated hypergamy only in the context of unequal educational pairings, excluding couples with equal levels of education (homogamy) from their analyses. Here, we argue that the prevalence of hypergamy should instead be assessed in relation to all marriages. We apply this approach to the case of Latin America, where women have made important gains in schooling relative to men. Using census microdata spanning 105 birth cohorts in 16 countries, we demonstrate that, rather than declining, hypergamy has increased in most countries over time and remains relatively stable across female educational advantage. Meanwhile, the prevalence of educational homogamy has declined considerably in most countries and across the axis of female educational advantage, an important trend that emerges only when homogamy is incorporated into the analysis. [ABSTRACT FROM AUTHOR]

While racial assortative mating and interracial unions have been a central interest in the study of race relations and family demography since the early twentieth century, there have been marked changes in the social contexts in which these processes have taken place in recent decades. This review article examines three important shifts: (a) the rise of population diversity and its impact on traditional views of racial integration, (b) the changing institution of marriage in American life, and (c) the increasing centrality of technology. We discuss how these societal shifts have challenged traditional understandings of preferences, opportunities, and intermediaries in the mate selection process, as well as new opportunities for interracial intimacy that these changes have introduced. We conclude with a discussion on conceptual issues and promising future research directions. [ABSTRACT FROM AUTHOR]

In this article, we analytically model marital sorting, intergenerational transfers, and inequality in a household optimization model with uncertainty. We modify and apply a 'sorting, reverse sorting' numerical approach by Demirtas in the context of marriage market mating, illustrating the robustness of our analytical results. We show that the parameters of the family production function play an important role in driving the path of an economy's inequality. One finding is that, under assortative mating, factor shares in the family production function positively affect inequality, while under disassortative mating, the relationship between the factor shares and inequality is U-shaped. This and other results that we obtain can stimulate further empirical research, holding potentially important policy implications. [ABSTRACT FROM AUTHOR]

Abstract Background According to the most recent U.S. CDC surveillance data, the rise in prevalence of childhood autism spectrum disorder among minority children has begun to outpace that of non-Hispanic white children. Since prior research has identified possible differences in the extent of mate selection for autistic traits across families of different ethnicity, this study examined variation in autism related traits in contemporaneous, epidemiologically ascertained samples of spousal pairs representing Hispanic and non-Hispanic white populations. The purpose was to determine whether discrepancies by ethnicity could contribute to differential increases in prevalence in the current generation of young children. Methods Birth records were used to identify all twin pairs born between 2011 and 2013 in California and Missouri. Families were selected at random from pools of English-speaking Hispanic families in California and Non-Hispanic White families in Missouri. Autistic trait data of parents was obtained using the Adult Report Form of the Social Responsiveness Scale (SRS-2). Results We did not identify a statistically significant difference in the degree of mate selection for autism related traits between Hispanic and non-Hispanic white spousal pairs. However, the degree of spousal correlation observed in this recent cohort was pronounced (on the order of ICC 0.45) and exceeded that typically reported in prior research (on the order of 0.30), surpassing also widely reported estimates for sibling correlation (also on the order of 0.30). Limitations The sample did not allow for a direct appraisal of change in the magnitude of spousal correlation over time and the ascertainments of trait burden were derived from spouse report. Conclusion Across two epidemiologically ascertained samples of spousal pairs representing Hispanic and non-Hispanic white families across two U.S. states (respectively, California and Missouri), the extent of autism-related trait co-variation for parents of the current generation of young children is substantial and exceeds correlations typically observed for siblings. Given the heritability of these traits and their relation to autism risk, societal trends in the degree of mate selection for these traits should be considered as possible contributors to subtle increases in the incidence of autism over time and across generations.

Existing methods for generating synthetic genotype data are ill-suited for replicating the effects of assortative mating (AM). We propose rb_dplr, a novel and computationally efficient algorithm for generating high-dimensional binary random variates that effectively recapitulates AM-induced genetic architectures using the Bahadur order-2 approximation of the multivariate Bernoulli distribution. The rBahadur R library is available through the Comprehensive R Archive Network at https://CRAN.R-project.org/package=rBahadur .

Parthenogenesis and interspecific mating are alternative reproductive strategies that species have evolved alternative strategies when the opportunity of sexual reproduction is hindered by the natural environment. However, it is still unclear how to make a choice between parthenogenesis and interspecific mating when females are unable to reproduce sexually with males of the same species.This study mainly investigated the reproductive behaviour of female termites in the absence of male termites of the same species. Here, reproductive behaviours of females Reticulitermes aculabialis (Ra♀) were observed when they encountered a male R. flaviceps (Rf♂) with the absence of male R. aculabialis(Ra♂).The results showed that Ra♀‐Rf♂ tandems were more prevalent and stable compared to Ra♀‐Ra♀ tandems. When a tandem inadvertently broke apart, the female R. aculabialis displayed longer pauses while waiting for male R. flaviceps, but shorter pauses when another female R. aculabialis was involved. Furthermore, there were mating behaviour between female R. aculabialis and males R. flaviceps, resulting in offspring produced in paired Ra♀‐Rf♂ colonies were hybridization between female R. aculabialis and male R. flaviceps.These results suggest that interspecific mating and recombination is an important aspect for the choice of reproduction strategy, which will provide new insights into the trade‐off between gene contribution rate and genetic diversity. [ABSTRACT FROM AUTHOR]

Abstract Background Positive assortative mating (AM) in several neuropsychiatric traits, including autism, has been noted. However, it is unknown whether the pattern of AM is different in phenotypically defined autism subgroups [e.g., autism with and without intellectually disability (ID)]. It is also unclear what proportion of the phenotypic AM can be explained by the genetic similarity between parents of children with an autism diagnosis, and the consequences of AM on the genetic structure of the population. Methods To address these questions, we analyzed two family-based autism collections: the Simons Foundation Powering Autism Research for Knowledge (SPARK) (1575 families) and the Simons Simplex Collection (SSC) (2283 families). Results We found a similar degree of phenotypic and ancestry-related AM in parents of children with an autism diagnosis regardless of the presence of ID. We did not find evidence of AM for autism based on autism polygenic scores (PGS) (at a threshold of |r|> 0.1). The adjustment of ancestry-related AM or autism PGS accounted for only 0.3–4% of the fractional change in the estimate of the phenotypic AM. The ancestry-related AM introduced higher long-range linkage disequilibrium (LD) between single nucleotide polymorphisms (SNPs) on different chromosomes that are highly ancestry-informative compared to SNPs that are less ancestry-informative (D2 on the order of 1 × 10−5). Limitations We only analyzed participants of European ancestry, limiting the generalizability of our results to individuals of non-European ancestry. SPARK and SSC were both multicenter studies. Therefore, there could be ancestry-related AM in SPARK and SSC due to geographic stratification. The study participants from each site were unknown, so we were unable to evaluate for geographic stratification. Conclusions This study showed similar patterns of AM in autism with and without ID, and demonstrated that the common genetic influences of autism are likely relevant to both autism groups. The adjustment of ancestry-related AM and autism PGS accounted for

Couple formation and assortative mating significantly influence societal structures, as marriages between individuals from diverse geographical or social backgrounds promote intra-family diversity. Understanding these patterns is crucial for grasping the demographic processes that shape contemporary societies. However, the scarcity of comprehensive data has impeded progress in this area. This paper aims to fill this gap by investigating assortative mating trends in the United States among birth cohorts from 1700 to 1910, utilizing data from FamiLinx, an online crowdsourced genealogical database. We focus on two primary dimensions: migration background (including natives, first and second-generation migrants) and age at marriage. Our analysis yields three major findings. First, we document significant changes in assortative mating trends over time, reflecting the dynamic nature of mate selection and its responsiveness to societal shifts. Second, we uncover substantial heterogeneity in assortative mating patterns across different social groups, indicating varying social dynamics and preferences. Third, we illustrate how these trends can be differently interpreted depending on whether the perspective is individual or familial. Additionally, we explore the advantages and limitations of using online genealogical data for historical studies of assortative mating, highlighting its potential for offering new insights while acknowledging the challenges posed by data quality and representativeness. [ABSTRACT FROM AUTHOR]

Background: Positive assortative mating (AM) in several neuropsychiatric traits, including autism, has been noted. However, it is unknown whether the pattern of AM is different in phenotypically defined autism subgroups [e.g., autism with and without intellectually disability (ID)]. It is also unclear what proportion of the phenotypic AM can be explained by the genetic similarity between parents of children with an autism diagnosis, and the consequences of AM on the genetic structure of the population. Methods: To address these questions, we analyzed two family-based autism collections: the Simons Foundation Powering Autism Research for Knowledge (SPARK) (1575 families) and the Simons Simplex Collection (SSC) (2283 families). Results: We found a similar degree of phenotypic and ancestry-related AM in parents of children with an autism diagnosis regardless of the presence of ID. We did not find evidence of AM for autism based on autism polygenic scores (PGS) (at a threshold of |r|> 0.1). The adjustment of ancestry-related AM or autism PGS accounted for only 0.3–4% of the fractional change in the estimate of the phenotypic AM. The ancestry-related AM introduced higher long-range linkage disequilibrium (LD) between single nucleotide polymorphisms (SNPs) on different chromosomes that are highly ancestry-informative compared to SNPs that are less ancestry-informative (D2 on the order of 1 × 10−5). Limitations: We only analyzed participants of European ancestry, limiting the generalizability of our results to individuals of non-European ancestry. SPARK and SSC were both multicenter studies. Therefore, there could be ancestry-related AM in SPARK and SSC due to geographic stratification. The study participants from each site were unknown, so we were unable to evaluate for geographic stratification. Conclusions: This study showed similar patterns of AM in autism with and without ID, and demonstrated that the common genetic influences of autism are likely relevant to both autism groups. The adjustment of ancestry-related AM and autism PGS accounted for < 5% of the fractional change in the estimate of the phenotypic AM. Future studies are needed to evaluate if the small increase of long-range LD induced by ancestry-related AM has impact on the downstream analysis. [ABSTRACT FROM AUTHOR]

Acoustic differentiation in bird vocalisations is a key process for speciation. Calls have received little attention compared to songs, but their simplicity facilitates analysis using mathematical, non-biased, tools, as they can be described by means of very basic variables. Here, we combined PERMANOVA and machine learning techniques to analyse the differentiation in the contact calls of the closely related Dartford (Curruca undata), Marmora's (C. sarda) and Balearic (C. balearica) warblers (formerly in the genus Sylvia). The calls of the three species differed clearly, consistent with phylogenetic reconstructions based on DNA sequences. In C. sarda, significant call differences were observed between the population wintering in Tunisia (migratory) and those of Sardinia and Corsica (mainly sedentary). Such divergence could be favoured by assortative mating of migrant and resident individuals, working as a matching mechanism for reproductive isolation in sympatry. In contrast, there was no clear separation between the accepted subspecies of C. undata. We found, however, significant differences between the Atlantic and Mediterranean biogeographical regions in this species. The divergences detected within C. undata and C. sarda deserve further investigation, using additional traits to elucidate the phylogenetic status of these groups, as well as the factors driving their diversification. [ABSTRACT FROM AUTHOR]

Background: Hyperactivity and inattention, the symptoms of ADHD, are marked by high levels of heritability and intergenerational transmission. Two distinct pathways of genetic intergenerational transmission are distinguished: direct genetic transmission when parental genetic variants are passed to the child's genome and genetic nurture when the parental genetic background contributes to the child's outcomes through rearing environment. This study assessed genetic contributions to hyperactivity and inattention in childhood through these transmission pathways. Methods: The sample included 415 families from the Quebec Newborn Twin Study. Twins' hyperactivity and inattention were assessed in early childhood by parents and in primary school by teachers. The polygenic scores for ADHD (ADHD‐PGS) and educational attainment (EA‐PGS) were computed from twins' and parents' genotypes. A model of intergenerational transmission was developed to estimate (1) the contributions of parents' and children's PGS to the twins' ADHD symptoms and (2) whether these variances were explained by genetic transmission and/or genetic nurture. Results: ADHD‐PGS explained up to 1.6% of the variance of hyperactivity and inattention in early childhood and primary school. EA‐PGS predicted ADHD symptoms at both ages, explaining up to 1.6% of the variance in early childhood and up to 5.5% in primary school. Genetic transmission was the only significant transmission pathway of both PGS. The genetic nurture channeled through EA‐PGS explained up to 3.2% of the variance of inattention in primary school but this association was non‐significant. Conclusions: Genetic propensities to ADHD and education predicted ADHD symptoms in childhood, especially in primary school. Its intergenerational transmission was driven primarily by genetic variants passed to the child, rather than by environmentally mediated parental genetic effects. The model developed in this study can be leveraged in future research to investigate genetic transmission and genetic nurture while accounting for parental assortative mating. [ABSTRACT FROM AUTHOR]

The evolution of behavioral isolation is often the first step toward speciation. While past studies show that behavioral isolation will sometimes evolve as a by-product of divergent ecological selection, we lack a more nuanced understanding of factors that may promote or hamper its evolution. The environment in which mating occurs may be important in mediating whether behavioral isolation evolves for two reasons. Ecological speciation could occur as a direct outcome of different sexual interactions being favored in different mating environments. Alternatively, mating environments may vary in the constraint they impose on traits underlying mating interactions, such that populations evolving in a "constraining" mating environment would be less likely to evolve behavioral isolation than populations evolving in a less constraining mating environment. In the latter, mating environment is not the direct cause of behavioral isolation but rather permits its evolution only if other drivers are present. We test these ideas with a set of 28 experimental fly populations, each of which evolved under one of two mating environments and one of two larval environments. Counter to the prediction of ecological speciation by mating environment, behavioral isolation was not maximal between populations evolved in different mating environments. Nonetheless, mating environment was an important factor as behavioral isolation evolved among populations from one mating environment but not among populations from the other. Though one mating environment was conducive to the evolution of behavioral isolation, it was not sufficient: assortative mating only evolved between populations adapting to different-larval environments within that mating environment, indicating a role for ecological speciation. Intriguingly, the mating environment that promoted behavioral isolation is characterized by less sexual conflict compared to the other mating environment. Our results suggest that mating environments play a key role in mediating ecological speciation via other axes of divergent selection. [ABSTRACT FROM AUTHOR]

We study changes in educational homogamy in the US and four European countries over the decade covering the Great Recession. The marital preferences identified point to the widening of the social gap between different educational groups since these preferences have increased the inclination of the individuals to match with others of similar educational traits in all five countries. We obtain this finding with an aggregate measure characterizing revealed preferences of individuals in relationship. We apply a novel approach for validating our finding: we compare our aggregate measure with dating data informative about the reservation points not only of those people who will be in a couple, but also those who will remain single. Finally, we challenge a commonly held view: we argue that marital preferences should not be blamed for the documented increase of the social gap since preferences are not exogenous, but are shaped by changes in the employment prospects of the potential partners. [ABSTRACT FROM AUTHOR]

Very recently, an interesting phenomenon was described in the common vole; vole parents with similar locomotor ability produced significantly larger litters. Positive assortative mating is a tendency to prefer individuals with similar phenotypes. We tested whether this also applies to smell similarity. Odour preference was tested in a T-maze, where each female was presented with two male odours, i.e. shavings together with feces and urine from home boxes. After female preference was established, the female was either paired with a preferred male (chosen) or paired with a non-preferred male (opposite choice). For analysis of the relationship to odour preference, genotyping of major histocompatibility complex (MHC) Class II DRB was done using amplicon sequencing. In the set of 45 individuals from two populations, we recovered 38 nucleotide haplotypes (alleles). Similarity of alleles in parent pairs according to the indexes of Sørensen–Dice (S–D) and Jaccard were calculated. Values of these indexes in parental pairs with preferred males were significantly higher (more similar) than in not preferred. The number of offspring in parental pairs with preferred males were significantly higher than in not preferred males. However, there is no correlation between the mentioned indexes and the number of offspring. The relationship between the success of reproduction and alleles is not clear-cut, this may be influenced by the measure of similarity we used, or by something that we could not detect. [ABSTRACT FROM AUTHOR]

With the increasing education of women in developing countries, educational assortative mating has become a significant aspect in the marriage market, with educational assortative mating patterns likely to be dependent on marriage timing. Using pooled data from three recent waves of the Cameroon Demographic and Health Surveys, the paper investigates the effect of marriage timing on educational assortative mating patterns in Cameroon. To achieve the objective, the study employed the Cox proportional hazard model and a control function version of multinomial Probit. Results show that delaying marriage is expected to decrease the likelihood of women engaging in low educationally homogamous marriages while increasing the probability of women entering high educationally homogamous and hypogamous marriages. Findings further depicted that over the period 2004–2018, the likelihood of women engaging in low educationally homogamous marriages decreased meanwhile the likelihood of women considering high educationally homogamous marriages and hypogamous marriages increased. The implications of these findings are in tandem with the wisdom that, programs encouraging the girl child to delay early marriages and stay longer in school can help women engage in high educationally homogamous marriages, empower women and thus improves their socioeconomic status. [ABSTRACT FROM AUTHOR]

The paradox between the ubiquity of polyploid lineages in plants and the early obstacles to the establishment of polyploids is a long‐studied yet unresolved question in evolutionary biology. It is assumed that to successfully persist after emergence, newly formed polyploids need to display certain fitness advantages and show a certain extent of reproductive isolation with their diploid progenitors. In this study, we tested whether immediate floral changes following polyploidization can improve pollinator visitation and enable pollinator preference leading to assortative mating, i.e. build a premating reproductive barrier between diploids and polyploids. For this purpose, we generated synthetic tetraploids of Arabidopsis arenosa and measured insect visitor behavior on diploids and synthetic tetraploids. We found that the increased floral size that accompanied polyploidization did not lead to a measurable increase in visitor preference, with insects visiting diploid and tetraploid plants at equal frequency. Despite this observation, tetraploids set more fruits than diploids, suggesting a positive impact of polyploidization on pollen transfer via other means. In addition, polyploidization did not lead to assortative mating but instead promoted interploidy pollen exchange, since visitors preferentially switched between cytotypes rather than preferring one. Consistent with this switching behavior, most of the progeny from tetraploid plants were triploid. Our data suggest that polyploidization has an immediate impact on mating in plants, but in a more complex way than has been assumed previously. [ABSTRACT FROM AUTHOR]

The strategic location of North Africa has led to cultural and demographic shifts, shaping its genetic structure. Historical migrations brought different genetic components that are evident in present-day North African genomes, along with autochthonous components. The Imazighen (plural of Amazigh) are believed to be the descendants of autochthonous North Africans and speak various Amazigh languages, which belong to the Afro-Asiatic language family. However, the arrival of different human groups, especially during the Arab conquest, caused cultural and linguistic changes in local populations, increasing their heterogeneity. We aim to characterize the genetic structure of the region, using the largest Amazigh dataset to date and other reference samples. Our findings indicate microgeographical genetic heterogeneity among Amazigh populations, modeled by various admixture waves and different effective population sizes. A first admixture wave is detected group-wide around the twelfth century, whereas a second wave appears in some Amazigh groups around the nineteenth century. These events involved populations with higher genetic ancestry from south of the Sahara compared to the current North Africans. A plausible explanation would be the historical trans-Saharan slave trade, which lasted from the Roman times to the nineteenth century. Furthermore, our investigation shows that assortative mating in North Africa has been rare. [ABSTRACT FROM AUTHOR]

The reversal of the gender gap in education has transformed traditional patterns of assortative mating, increasing the number of hypogamous couples. This change has been particularly intense in the case of Spain, a country of great interest due to the ambivalence of strong support for egalitarian attitudes and high proportion of traditional couples. Using quarterly microdata from the Spanish Labour Force Survey, applying generalised ordered-logit models, this research reveals that educational hypogamy increases the probability of occupational hypogamy. This association is consistent with the use of different occupational classifications and levels of disaggregation. But there are some factors that limit the transmission of women's educational advantages to their occupational levels, mainly gender differences in access to the labour market and an uneven distribution of professional achievements by sex. The findings obtained underline the relevance of using different measures as well as different theoretical approaches to explain seemingly contradictory couple equilibria. [ABSTRACT FROM AUTHOR]

Vocal rhythm plays a fundamental role in sexual selection and species recognition in birds, but little is known of its genetic basis due to the confounding effect of vocal learning in model systems. Uncovering its genetic basis could facilitate identifying genes potentially important in speciation. Here we investigate the genomic underpinnings of rhythm in vocal non-learning Pogoniulus tinkerbirds using 135 individual whole genomes distributed across a southern African hybrid zone. We find rhythm speed is associated with two genes that are also known to affect human speech, Neurexin-1 and Coenzyme Q8A. Models leveraging ancestry reveal these candidate loci also impact rhythmic stability, a trait linked with motor performance which is an indicator of quality. Character displacement in rhythmic stability suggests possible reinforcement against hybridization, supported by evidence of asymmetric assortative mating in the species producing faster, more stable rhythms. Because rhythm is omnipresent in animal communication, candidate genes identified here may shape vocal rhythm across birds and other vertebrates. Little is known about the genetic basis of the rhythmic component of bird song, an important trait in sexual selection and species recognition. By studying a system with innate vocalizations, the Pogoniulus tinkerbirds, this study finds candidate genes that underlie differences in speed in vocal rhythm in this system. [ABSTRACT FROM AUTHOR]

A central aim of genome-wide association studies (GWASs) is to estimate direct genetic effects: the causal effects on an individual's phenotype of the alleles that they carry. However, estimates of direct effects can be subject to genetic and environmental confounding and can also absorb the "indirect" genetic effects of relatives' genotypes. Recently, an important development in controlling for these confounds has been the use of within-family GWASs, which, because of the randomness of mendelian segregation within pedigrees, are often interpreted as producing unbiased estimates of direct effects. Here, we present a general theoretical analysis of the influence of confounding in standard population-based and within-family GWASs. We show that, contrary to common interpretation, family-based estimates of direct effects can be biased by genetic confounding. In humans, such biases will often be small per-locus, but can be compounded when effect-size estimates are used in polygenic scores (PGSs). We illustrate the influence of genetic confounding on population- and family-based estimates of direct effects using models of assortative mating, population stratification, and stabilizing selection on GWAS traits. We further show how family-based estimates of indirect genetic effects, based on comparisons of parentally transmitted and untransmitted alleles, can suffer substantial genetic confounding. We conclude that, while family-based studies have placed GWAS estimation on a more rigorous footing, they carry subtle issues of interpretation that arise from confounding. GWASs aim to estimate direct effects of genotype on an individual's phenotype, but this can be subject to genetic and environmental confounds and "indirect" genetic effects of relatives' genotypes. This study presents a theoretical analysis of the influence of confounders in population-based and within-family GWASs, showing that, while family-based studies are more rigorous, they still carry subtle issues that arise from confounding. [ABSTRACT FROM AUTHOR]

Previous studies have found a high degree of assortative mating for educational attainment (r =.56). However, this can be confounded by cohort effects or country effects, where certain nations may have more pronounced assortative mating than others. In addition, method variance regarding how educational attainment is measured may also result in heterogeneity of effect sizes. Effect sizes were gathered from various datasets and from academic literature, resulting in a large collection of effect sizes (k = 1498, n = 9,159,098), spanning 84 different countries. Assortative mating for educational attainment was stronger than what previous literature suggested (r =.66, [.64,.68]), largely due to the fact that assortative mating for educational attainment is stronger when latent methods are used. The strongest predictors of assortative mating for education between countries were individualism (r = −.61, p <.001) and HDI (r = −.56, p <.001). Assortative mating over time was found to vary by region. Capitalist Europe experienced an increase in assortative mating for education, while Communist Europe experienced a decrease. The United States had a non-linear trend in assortative mating for educational attainment, as it decreased from 1875 to 1926, increased from 1926 to 1945, decreased from 1945 to 1958, increased from 1958 to 1977, and decreased from 1977 onwards. [ABSTRACT FROM AUTHOR]

Mating in animal communities must be managed in a way that assures the performance increase in the progenies without increasing the rate of inbreeding. It has currently become possible to identify millions of single nucleotide polymorphisms (SNPs), and it is feasible to select animals based on genome-wide marker profiles. This study aimed to evaluate the impact of five mating designs among individuals (random, positive and negative assortative, minimized and maximized inbreeding) on genomic prediction accuracy. The choice of these five particular mating designs provides a thorough analysis of the way genetic diversity, relatedness, inbreeding, and biological conditions influence the accuracy of genomic predictions. Utilizing a stochastic simulation technique, various marker and quantitative trait loci (QTL) densities were taken into account. The heritabilities of a simulated trait were 0.05, 0.30, and 0.60. A validation population that only had genotypic records was taken into consideration, and a reference population that had both genotypic and phenotypic records was considered for every simulation scenario. By measuring the correlation between estimated and true breeding values, the prediction accuracy was calculated. Computing the regression of true genomic breeding value on estimated genomic breeding value allowed for the examination of prediction bias. The scenario with a positive assortative mating design had the highest accuracy of genomic prediction (0.733 ± 0.003 to 0.966 ± 0.001). In a case of negative assortative mating, the genomic evaluation's accuracy was lowest (0.680 ± 0.011 to 0.899 ± 0.003). Applying the positive assortative mating design resulted in the unbiased regression coefficients of true genomic breeding value on estimated genomic breeding value. Based on the current results, it is suggested to implement positive assortative mating in genomic evaluation programs to obtain unbiased genomic predictions with greater accuracy. This study implies that animal breeding programs can improve offspring performance without compromising genetic health by carefully managing mating strategies based on genetic diversity, relatedness, and inbreeding levels. To maximize breeding results and ensure long-term genetic improvement in animal populations, this study highlights the importance of considering different mating designs when evaluating genomic information. When incorporating positive assortative mating or other mating schemes into genomic evaluation programs, it is critical to consider the complex relationship between gene interactions, environmental influences, and genetic drift to ensure the stability and effectiveness of breeding efforts. Further research and comprehensive analyzes are needed to fully understand the impact of these factors and their possible complex interactions on the accuracy of genomic prediction and to develop strategies that optimize breeding outcomes in animal populations.

ABSTRACTThe strong negative correlation between divorce and a wide range of outcomes in terms of well-being, health, education and labour market performance has been well documented in the literature. Economic conditions have been found to affect marital stability. Shared gains from marriage also depend on spouses’ characteristics such as age, education, ethnicity and religious beliefs. This paper examines the relationship between these spousal characteristics and the probability of dissolution while taking into account business cycle fluctuations. Using data from the Panel Study of Income Dynamics 1968–2011 for the United States and employing a duration modelling strategy, findings reveal that differences in educational attainment and ethnicity between spouses increase the hazard of marital dissolution. However similarity in religious beliefs and ethnicity reduce the risk of divorce. A period of economic growth improves marital stability. However, ethnic differences are a significant predictor of marital division, even in times of economic prosperity.

The bright colors of Alpine leaf beetles (Coleoptera, Chrysomelidae) are thought to act as aposematic signals against predation. Within the European Alps, at least six species display a basal color of either blue or green, likely configuring a classic case of müllerian mimicry. In this context, intra-population color polymorphism is paradoxical as the existence of numerous color morphs might hamper the establishment of a search image in visual predators. Assortative mating may be one of the main factors contributing to the maintenance of polymorphic populations. Due to the marked iridescence of these leaf beetles, the perceived color may change as the viewing or illumination angle changes. The present study, conducted over three years, involved intensive sampling of a population of Oreina gloriosa from the Italian Alps and applied colorimetry and a decision tree method to identify the color morphs in an objective manner. The tertiary sex ratio of the population was biased in favor of males, suggesting that viviparous females hide to give birth. Seven color morphs were identified, and their frequencies varied significantly over the course of the study. Three different analyses of mating (JMating, QInfomating, and Montecarlo simulations) recognized a general trend for random mating which coexists with some instances of positive and negative assortative mating. This could help explain the pre-eminence of one morph (which would be favored because of positive selection due to positive assortative mating) in parallel with the persistence of six other morphs (maintained due to negative assortative mating). [ABSTRACT FROM AUTHOR]

Assortative mating – the non-random mating of individuals with similar traits – is known to increase trait-specific genetic variance and genetic similarity between relatives. However, empirical evidence is limited for many traits, and the implications hinge on whether assortative mating has started recently or many generations ago. Here we show theoretically and empirically that genetic similarity between relatives can provide evidence on the presence and history of assortative mating. First, we employed path analysis to understand how assortative mating affects genetic similarity between family members across generations, finding that similarity between distant relatives is more affected than close relatives. Next, we correlated polygenic indices of 47,135 co-parents from the Norwegian Mother, Father, and Child Cohort Study (MoBa) and found genetic evidence of assortative mating in nine out of sixteen examined traits. The same traits showed elevated similarity between relatives, especially distant relatives. Six of the nine traits, including educational attainment, showed greater genetic variance among offspring, which is inconsistent with stable assortative mating over many generations. These results suggest an ongoing increase in familial similarity for these traits. The implications of this research extend to genetic methodology and the understanding of social and economic disparities. Non-random mating can complicate genetic studies, but implications hinge on its history in prior generations. Here, the authors use genetic similarity between relatives to investigate which traits show evidence of recent changes in mating behavior. [ABSTRACT FROM AUTHOR]

Aim: Hybridization is thought to have played an important role in shaping the evolutionary history of diverse island taxa. Here, we propose an ecological and evolutionary framework for understanding the causes and consequences of heterospecific mating on islands—with and without introgressive hybridization. We use this framework to support our main contention that cases of secondary contact among endemic species should commonly result in introgressive hybridization whereas cases of contact between endemic and introduced species should commonly result in reproductive interference (RIN)—resulting in two qualitatively different faces of secondary contact on islands. Location: Canary Islands, Galapagos, New Zealand, Caribbean and Hawaii. Taxa: 705 vertebrate, invertebrate and plant species spanning 167 genera and 99 families. Methods: Using a quantitative analysis of empirical research on secondary contact on islands, we weigh evidence for the causes and consequences of secondary contact and heterospecific mating on islands. In particular, we compare cases of secondary contact between endemic species versus secondary contact between endemic and introduced species. Results: We find that the drivers of secondary contact and heterospecific mating on islands most frequently reported in the literature are disturbance, long‐distance (e.g. inter‐island) dispersal and compromised assortative mating. We find support for the hypothesis that extensive introgression is a more common outcome between endemic species while RIN is a more common outcome between endemic and introduced species. Main Conclusions: We conclude that there are biological reasons to predict secondary contact and heterospecific mating to be common on islands for all taxa, but that the consequence of secondary contact is categorically different for contact between endemic species and contact between endemic and introduced species. We conclude that the former likely explains the apparent frequency of hybridization on islands, while the latter presents a cryptic and underappreciated conservation threat. [ABSTRACT FROM AUTHOR]

Colour polymorphisms have long served as model systems in evolutionary studies and continue to inform about processes involved in the origin and dynamics of biodiversity. Modern sequencing tools allow for evaluating whether phenotypic differences between morphs reflect genetic differentiation rather than developmental plasticity, and for investigating whether polymorphisms represent intermediate stages of diversification towards speciation. We investigated phenotypic and genetic differentiation between two colour morphs of the butterfly Fabriciana adippe using a combination of ddRAD‐sequencing and comparisons of body size, colour patterns and optical properties of bright wing spots. The silvery‐spotted adippe form had larger and darker wings and reflected UV light, while the yellow cleodoxa form displayed more green scales and reflected very little UV, showcasing that they constitute distinct and alternative integrated phenotypes. Genomic analyses revealed genetic structuring according to source population, and to colour morph, suggesting that the phenotypic differentiation reflects evolutionary modifications. We report 17 outlier loci associated with colour morph, including ultraviolet‐sensitive visual pigment (UVRh1), which is associated with intraspecific communication and mate choice in butterflies. Together with the demonstration that the wings of the adippe (but essentially not the cleodoxa) morph reflect UV light, that UV reflectance is higher in females than males and that morphs differ in wing size, this suggests that these colour morphs might represent genetically integrated phenotypes, possibly adapted to different microhabitats. We propose that non‐random mating might contribute to the differentiation and maintenance of the polymorphism. [ABSTRACT FROM AUTHOR]

Traits under divergent ecological selection that also function during mating can be important in maintaining species boundaries. Few studies have considered mutual mate choice, where both males and females base mating decisions on the same trait. Wing colouration in Heliconius butterflies evolved as a warning signal but also functions as a mating cue. We investigated the contribution of visual preference to assortative mating in an aposematic butterfly Heliconius cydno in the context of reproductive isolation with its sympatric, visually distinct relative Heliconius melpomene. Heliconius cydno have conspicuous white bands on their forewings, whereas those of H. melpomene are red in colour. We predicted that both sexes of H. cydno contributed to assortative mating by exhibiting visual preference towards conspecific wing colouration. We analysed published and new data from preference experiments, in which males were presented with conspecific and H. melpomene females. We also recorded female responses and mating outcomes in choice experiments, involving conspecific males with either the original white or artificially painted red forewing bands. Both sexes of H. cydno responded more positively towards the conspecific colouration, and males strongly preferred females of its own colours. In contrast, male colouration did not predict mating outcomes in female choice experiments. As courtships are initiated by males in butterflies, our findings suggest that female visual preference might be of secondary importance in H. cydno. Our data also suggest that the contribution of visual preference to reproductive isolation might be unequal between H. cydno and its sympatric relative H. melpomene. [ABSTRACT FROM AUTHOR]

Risk taking behaviour — how individuals perceive and respond to threat — varies among individuals. In birds, this behaviour influences the choice of nest microhabitat presumably because exposure to predation depends on the structural composition of the nest microhabitat (i.e., a small area where a bird builds its nest). Thus, a chosen nest microhabitat can indicate an adaptation to predation risk. However, where both parents participate in or share breeding roles, it is unknown whether the chosen nest microhabitat is influenced by risk taking behaviour of the female, the male or both parents. Moreover, risk taking may affect other behaviours during breeding, thus having a partner with similar risk taking behaviour may be important for pair complementarity. We investigated risk taking behaviour of breeding Kentish plovers (Charadrius alexandrinus) using flight initiation distance (FID) as a proxy. First, we tested whether FID is repeatable. Second, we tested whether members of breeding pairs have similar FID. Third, we investigated whether male and female's FID is associated with the choice of nest microhabitat. We classified nest microhabitat by two indices: cover directly above the nest scrape (above nest cover) and cover around the nest (around nest coverage). We found that (i) FID was highly repeatable, (ii) FID was correlated within members of breeding pairs and (iii) female's risk taking behaviour is linked to the use of around nest coverage. Specifically, females with longer FID, (i.e., more risk-averse ones) tended to use less concealed nest microhabitat. We concluded that nest microhabitat choice in the Kentish plovers is likely a reflection of the female's risk taking behaviour. Breeding partners likely have similar risk taking behaviour, an indication of assortative mating. We advocate partitioning of correlation within breeding pairs to ascertain estimates of within pair correlation attributable to assortative mating. [ABSTRACT FROM AUTHOR]

In the animal kingdom, sexually dimorphic color variation is a widespread phenomenon that significantly influences survival and reproductive success. However, the genetic underpinnings of this variation remain inadequately understood. Our investigation into sexually dimorphic color variation in the desert-dwelling Guinan population of the toad-headed agamid lizard (Phrynocephalus putjatai) utilized a multidisciplinary approach, encompassing phenotypic, ultrastructural, biochemical, genomic analyses, and behavioral experiments. Our findings unveil the association between distinct skin colorations and varying levels of carotenoid and pteridine pigments. The red coloration in males is determined by a genomic region on chromosome 14, housing four pigmentation genes: BCO2 and three 6-pyruvoyltetrahydropterin synthases. A Guinan population-specific nonsynonymous single nucleotide polymorphism in BCO2 is predicted to alter the electrostatic potential within the binding domain of the BCO2-β-carotene complex, influencing their interaction. Additionally, the gene MAP7 on chromosome 2 emerges as a potential contributor to the blue coloration in subadults and adult females. Sex-specific expression patterns point to steroid hormone-associated genes (SULT2B1 and SRD5A2) as potential upstream regulators influencing sexually dimorphic coloration. Visual modeling and field experiments support the potential selective advantages of vibrant coloration in desert environments. This implies that natural selection, potentially coupled with assortative mating, might have played a role in fixing color alleles, contributing to prevalence in the local desert habitat. This study provides novel insights into the genetic basis of carotenoid and pteridine-based color variation, shedding light on the evolution of sexually dimorphic coloration in animals. Moreover, it advances our understanding of the driving forces behind such intricate coloration patterns. [ABSTRACT FROM AUTHOR]

We analyze economic assortative mating and its contribution to earnings inequality in South Korea from 1998 to 2018. Our analysis is based on cross-sectional and panel data and accounts for several methodological issues, including measurement error and sample selection bias. Despite a very high level of assortativeness in education, Korea exhibits a negative correlation in earnings between spouses due to low female labor force participation and its negative correlation with male earnings. However, the correlation is large and positive for hourly earnings, among dual-earner couples. Cohort analysis reveals significant changes in earnings correlations, as rising female labor force participation offsets slightly declining educational sorting among younger cohorts. As a result, assortative mating contributes to a very limited extent to inequality between households in observed monthly earnings, but accounts for a sizable fraction, around to 15%, of inequality between household in hourly earnings. [ABSTRACT FROM AUTHOR]

Mendelian randomization (MR) is a popular epidemiologic study design that uses genetic variants as instrumental variables (IVs) to estimate causal effects, while accounting for unmeasured confounding. The validity of the MR design hinges on certain IV assumptions, which may sometimes be violated due to dynastic effects, population stratification, or assortative mating. Since these mechanisms act through parental factors it was recently suggested that the bias resulting from violations of the IV assumptions can be reduced by combing the MR design with the sibling comparison design, which implicitly controls for all factors that are constant within families. In this article, we provide a formal discussion of this combined MR‐sibling design. We derive conditions under which the MR‐sibling design is unbiased, and we relate these to the corresponding conditions for the standard MR and sibling comparison designs. We proceed by considering scenarios where all three designs are biased to some extent, and discuss under which conditions the MR‐sibling design can be expected to have less bias than the other two designs. We finally illustrate the theoretical results and conclusions with an application to real data, in a study of low‐density lipoprotein and diastolic blood pressure using data from the Swedish Twin Registry. [ABSTRACT FROM AUTHOR]

Wing dimorphism is a life‐historical trait of insects which indicates the developmental trend of populations, going as migrants or staying as residents. The alternative wing morph enhances adaptability of insects to changing environments. However, the underlying mechanism for maintaining wing dimorphism remains vague. The brown planthoppers Nilaparvata lugens, a serious pest of rice, are either short‐winged or long‐winged. The shift between two wing morphs is determined by two insulin receptors. So, this pest is a better model organism to explore the mechanism of wing dimorphism. Here, the short‐ and long‐winged strains of N. lugens were selected. Rates of a selected wing morph were linearly increased in populations, and the selection response of the short‐winged morph was stronger than that of the long‐winged. Selection enhanced the migratory or resident propensity. Directional selection for the long‐winged morph resulted in longer and lighter forewings, while selection for the short‐winged morph generated shorter and thicker wings and higher fecundity. Relative expression levels of wing development genes InR1, InR2 and Foxo were positively correlated with the short‐winged rate in the short‐winged strain, while they were negatively correlated with the long‐winged rate in the long‐winged strain at specific stages. The change rate of expression levels was approximately two times as high as that of the wing morph rates in populations, indicating a high threshold‐dependent gene expressed regulation of wing morph. A partial assortative mating behavior occurred between the nearly pure‐bred lineages of short‐ and long‐winged strains. The short‐winged males preferred to mate with short‐winged females while the long‐winged males mated with the short‐ and long‐winged females equally. The threshold‐dependent mode may be more flexible to adjust wing morphs according to environmental conditions and the partial assortative mating promotes the genetic exchange between two wing morphs which drive the maintenance of wing dimorphism. [ABSTRACT FROM AUTHOR]

The process of speciation generates biodiversity. According to the null model of speciation, barriers between populations arise in allopatry, where, prior to biology, geography imposes barriers to gene flow. On the other hand, sympatric speciation requires that the process of speciation happen in the absence of a geographical barrier, where the members of the population have no spatial, temporal barriers. Several attempts have been made to theoretically identify the conditions in which speciation can occur in sympatry. However, these efforts suffer from several limitations. We propose a model for sympatric speciation based on adaptation for resource utilization. We use a genetics-based model to investigate the relative roles of prezygotic and postzygotic barriers, from the context of ecological disruptive selection, sexual selection, and genetic architecture, in causing and maintaining sympatric speciation. Our results show that sexual selection that acts on secondary sexual traits does not play any role in the process of speciation in sympatry and that assortative mating based on an ecologically relevant trait forces the population to show an adaptive response. We also demonstrate that understanding the genetic architecture of the trait under ecological selection is very important and that it is not required for the strength of ecological disruptive selection to be very high in order for speciation to occur in sympatry. Our results provide an insight into the kind of scenarios in which sympatric speciation can be demonstrated in the lab. [ABSTRACT FROM AUTHOR]

Cultural and socioeconomic differences stratify human societies and shape their genetic structure beyond the sole effect of geography. Despite mating being limited by sociocultural stratification, most demographic models in population genetics often assume random mating. Taking advantage of the correlation between sociocultural stratification and the proportion of genetic ancestry in admixed populations, we sought to infer the former process in the Americas. To this aim, we define a mating model where the individual proportions of the genome inherited from Native American, European, and sub-Saharan African ancestral populations constrain the mating probabilities through ancestry-related assortative mating and sex bias parameters. We simulate a wide range of admixture scenarios under this model. Then, we train a deep neural network and retrieve good performance in predicting mating parameters from genomic data. Our results show how population stratification, shaped by socially constructed racial and gender hierarchies, has constrained the admixture processes in the Americas since the European colonization and the subsequent Atlantic slave trade. [ABSTRACT FROM AUTHOR]

The forces of evolution—mutation, selection, migration, and genetic drift—shape the genetic architecture of human traits, including the genetic architecture of complex neuropsychiatric illnesses. Studying these illnesses in populations that are diverse in genetic ancestry, historical demography, and cultural history can reveal how evolutionary forces have guided adaptation over time and place. A fundamental truth of shared human biology is that an allele responsible for a disease in anyone, anywhere, reveals a gene critical to the normal biology underlying that condition in everyone, everywhere. Understanding the genetic causes of neuropsychiatric disease in the widest possible range of human populations thus yields the greatest possible range of insight into genes critical to human brain development. In this perspective, we explore some of the relationships between genes, adaptation, and history that can be illuminated by an evolutionary perspective on studies of complex neuropsychiatric disease in diverse populations. Members of the NIMH Network for Studies of Mental Disorders in Ancestrally Diverse Populations illuminate the genetic architecture of complex neuropsychiatric illnesses in the context of forces of evolution: mutation, selection, migration, and genetic drift/population structure. [ABSTRACT FROM AUTHOR]

Introgressive hybridization caused by invasive species may lead to the extinction of pure native species, but a theoretical model of the invasion process with hybridization (the neutral demographic model) suggests that introgression occurs mainly from native to invasive species. Clarifying the direction of introgression is important to evaluate the impact of hybridization on native species. In southern Japan, a widely disseminated gecko, Gekko hokouensis , and a local gecko, Gekko yakuensis , have formed mosaic hybrid zones. Given the presumed invasiveness of Gekko hokouensis , the neutral demographic model predicts that introgression would mainly occur in the direction to Gekko hokouensis , whereas possible asymmetric assortative mating suggested by a previous study predicts the opposite direction of introgression. Our investigations using microsatellite markers and mitochondrial DNA for the gecko assemblages in 12 localities and comparisons with allozyme data collected 18 years ago indicated that Gekko hokouensis expanded its range and tended to have replaced hybrids and Gekko yakuensis. Introgression was skewed towards Gekko hokouensis , but interspecific mating between the parental species was reciprocal. These results suggest that their hybridization progress follows the neutral demographic model and that the higher population growth rate of Gekko hokouensis is the major cause of species replacement, although we cannot rule out the possibility that asymmetric assortative mating also influences the later stages of species replacement. [ABSTRACT FROM AUTHOR]

Work on the Lake Victoria cichlids Pundamilia nyererei (red dorsum males, deeper water), Pundamilia pundamilia (blue males, shallower water) and related species pairs has provided insights into processes of speciation. Here, we investigate the female mating behaviour of 5 Pundamilia species and 4 of their F1 hybrids through mate choice trials and paternity testing. Complete assortative mating was observed among all sympatric species. Parapatric species with similar depth habitat distributions interbred whereas other parapatric and allopatric species showed complete assortative mating. F1 hybrids mated exclusively with species accepted by females of the parental species. The existence of complete assortative mating among some currently allopatric species suggests that pre-existing mating barriers could be sufficient to explain current patterns of co-existence, although, of course, many other factors may be involved. Regardless of the mechanism, mating preferences may influence species distribution in potentially hybridizing taxa, such as in the adaptive radiation of cichlid fish. We suggest that this at least partly explains why some species fail to establish breeding populations in locations where they are occasionally recorded. Our results support the notion that the mating preferences of potentially cross-breeding species ought to be included in coexistence theory. [ABSTRACT FROM AUTHOR]

While numerous theoretical population genetic models predict that mating assortatively by genetic "quality" will enhance the efficiency of purging of deleterious mutations and/or the spread of beneficial alleles in the gene pool, empirical examples of assortative mating by quality are surprisingly rare and often inconclusive. Here, we set out to examine whether fruit flies (Drosophila melanogaster) engage in assortative mating by body-size phenotype, a composite trait strongly associated with both reproductive success and survival and is considered a reliable indicator of natural genetic quality. Male and female flies of different body-size classes (large and small) were obtained under typical culture conditions, which allows us to use standing variation of body size without involving artificial nutritional manipulation, so that their interactions and mating patterns could be measured. While flies did not exhibit assortative courtship behavior, when patterns of offspring production were analyzed, it was found that individuals produced more offspring with partners of similar quality/body size, resulting produced from disassortative mating. Together, these results validate theoretical predictions that sexual selection can enhance the effects of natural selection and consequently the rate of adaptive evolution in a positive correlation in fitness between mates. Subsequent assays of offspring fitness indicated that assortative mating produced sons and daughters that had greater or equal reproductive success than those [ABSTRACT FROM AUTHOR]

We analyzed two morpho-species, Astyanax aeneus and Astyanax caballeroi, coexisting in Lake Catemaco, with ecological differences previously associated with different trophic niches. While A. aeneus is a widely distributed species, A. caballeroi is endemic to Lake Catemaco. Due to the contrasting morphology between these two sympatric species, they were originally assigned to different genera, but little is known about their genetic differentiation. We hypothesized that these two species, which present differentiation in morphology and in trophic niches, co-occur in concomitance with assortative mating and form distinct genetic clusters. We tested this prediction by typing a set of 12 microsatellites in 348 individuals of the two morpho-species, comparing their genetic structure patterns with that of an allopatric population of A. aeneus (i.e., the Maquinas population). Genetic structure analysis, assignment analyses, and estimation of gene flow between the sympatric morpho-species were carried out. Contrary to expectations, there is a lack of genetic differentiation between the A. aeneus and A. caballeroi morpho-species. However, there was a genetic differentiation between Lake Catemaco and Río Maquinas populations of A. aeneus. In addition, we found an asymmetric gene flow pattern, with a larger migration rate from A. aeneus to A. caballeroi than in the other direction. Finally, the allopatric population of A. aeneus showed lower levels of genetic diversity than those reported for both morpho-species in the lacustrine system. Consequently, our results support the notion that these morpho-species are either in an early phase of speciation or represent a single polymorphic species. This model provides relevant information to understanding the presence of polymorphisms under gene flow and their potential impact on the speciation process. [ABSTRACT FROM AUTHOR]