Marriage structure of residents of Kharkhov in relation to genetically significant socio-demographic characteristics

Positive assortative mating for education and profession has been revealed by means of sample analysis of couples married in two districts of Kharkov in 1960 and 1985. The contingency coefficient measuring the association between education of husband and wife in 1985 was K = 0.27 in one and K = 0.35 in the other district. The degree of assortative mating for profession was K = 0.57 and K = 0.19 in 1960, K = 0.27 and K = 0.31 in 1985, in two districts, respectively.     

The role of migration processes in the formation of marriage structure of Moscow population. II. Assortative mating for the age, birthplace and nationality

Positive assortative mating for age at marriage, birthplace and nationality has been revealed by means of sample analysis of couples married in Moscow in 1955 and 1980. The correlation coefficient between mates for age at marriage was r = 0.81 in 1955 and r = 0.88 in 1980; the age difference between spouses had a mean of 1.55 and 2.21 years, respectively. The determinative role of migration in forming Moscow population marriage structure accounts for the fact that the greater part of marriages registered in the capital are between migrants from various regions of the USSR or between the Moscow-born and the migrants. The proportion of marriages between individuals born in Moscow has increased over 25 years from 10 to 38%, these values being significantly higher than those expected under random mating between the migrants and the Moscow-born. The contingency coefficient measuring the association between the birthplaces of husband and wife was K = 0.16 in 1955 and K = 0.11 in 1980, the preferential marriage between mates born in the same region being still significant even when marriages are registered in Moscow. The highest degrees of assortative mating were observed for nationality character: K = 0.37 in 1955 and K = 0.28 in 1980. The decrease in these values over the past 25 years has resulted in a slight growth of the proportion of international marriages (from 14.75 to 16.53%) which has not yet reached the level expected under panmixia (about 21%).     

Genetic demographic parameters of the marriage structure of the Yevpatoria population

Records on marriages contracted in the city of Yevpatoria, Ukraine in 1960/1961, 1985, 1993, and 1994/1995 were used to determine some parameters of the city population structure. The coefficients of correlation with respect to the age of marriage in reproductive-age couples contracting marriages in these years were 0.77, 0.81, and 0.80, respectively. Women that contracted marriages at reproductively unfavorable ages (under 20 and over 30 years) in the respective years constituted 28.3, 40.6, and 45.4% of the total sample. The proportions of interethnic marriages in these years were 39.4, 43.9, and 46.6%. The proportion of Slavs decreased from 94 to 91% during 35 years, but the proportion of Ukrainians increased from 23.1 to 26.5%. The proportion of other ethnic groups (Tatars, Armenians, Karaites, Poles, Germans, etc.) increased from 3 to 8.6%. The marriage contingency with respect to ethnicity (K = 0.26 in 1960/1961, K = 0.22 in 1985, and K = 0.28 in 1994/1995) was higher than with respect to education (K = 0.18 in 1985 and K = 0.23 in 1993) or occupation (K = 0.18 in 1960/1961, K = 0.17 in 1985, and K = 0.23 in 1994/1995). The marriage assortativeness with respect to ethnicity was the highest in ethnic minorities (A' = 55.1%); that with respect to education, in persons who had higher or primary education (A' = 40.1% and A'= 78.0%, respectively); and that with respect to occupation, in students, military personnel, and production workers (60.6, 58.7, and 30.9%).     

Sexual size dimorphism and assortative mating for morphological traits in Passer domesticus

In this study, assortative mating for different morphological traits was studied in a captive population of house sparrows (Passer domesticus). Males were larger than females. Assortative mating was found for tail length, wing length and general body size. Males with larger badge size mated with females with longer tails. The strongest assortative mating occurred for tail length (r=0.77), and this assortative mating remained significant after controlling for wing length, mass and tarsus length, suggesting that it was not an artefact of assortative mating for body size. The possibility of sexual selection for tail length in the house sparrow is discussed.     

Genetic demographic structure of the Belgorod population: age, ethnicity, education, and occupation

Data from marriage records of the city of Belgorod for 1960, 1985, and 1995 have been used to determine some parameters of population structure in this city. The coefficients of correlation with respect to age of marriage between spouses in the couples contracting marriages in these years were 0.74, 0.62, and 0.80, respectively. Women of reproductively unfavorable age (under 20 or over 30 years) accounted for 5.5, 0.83, and 19% of all women contracting marriages in these years, respectively. The proportions of interethnic marriages in these years were 16.9, 14.9, and 15.6%, respectively. The percentage of Slavs decreased from 99 to 97% during the 35 years studied, whereas the proportion of Russians insignificantly increased (from 90.4 to 91.4%). The proportion of Caucasian ethnic groups increased by six time (from 0.3 to 1.8%), and that of other non-Slavic ethnic groups increased by almost two times (from 0.7 to 1.2%). The marriage convergence (K) with respect to ethnicity (0.095, 0.106, and 0.090 in 1960, 1985, and 1995, respectively) was lower than that with respect to education (0.296 and 0.350 in 1985 and 1995, respectively) or occupation (0.212 and 0.231 in 1985 and 1995, respectively). The maximum coefficients of ethnically, educationally, and occupationally assortative marriage have been found, respectively, in ethnic minority groups (A' = 20%); in persons with higher and primary education (A' = 37.5 and A' = 49.9%, respectively); and in the military officers/soldiers, engineers, healthcare professionals, and researchers (the respective A' values are 65.6, 32.2, 31.5, and 39.8%).     

Negative‐assortative mating for color in wolves

There is strong negative‐assortative mating for gray and black pelage color in the iconic wolves in Yellowstone National Park. This is the first documented case of significant negative‐assortative mating in mammals and one of only a very few cases in vertebrates. Of 261 matings documented from 1995 to 2015, 63.6% were between gray and black wolves and the correlation between mates for color was –0.266. There was a similar excess of matings of both gray males × black females and black males × gray females. Using the observed frequency of negative‐assortative mating in a model with both random and negative‐assortative mating, the estimated proportion of negative‐assortative mating was 0.430. The estimated frequency of black wolves in the population from 1996 to 2014 was 0.452 and these frequencies appear stable over this 19‐year period. Using the estimated level of negative‐assortative mating, the predicted equilibrium frequency of the dominant allele was 0.278, very close to the mean value of 0.253 observed. In addition, the patterns of genotype frequencies, that is, the observed proportion of black homozygotes and the observed excess of black heterozygotes, are consistent with negative‐assortative mating. Importantly these results demonstrate that negative‐assortative mating could be entirely responsible for the maintenance of this well‐known color polymorphism.     

Direct and indirect assortative mating: a multivariate approach to plant flowering schedules

This paper develops methods to partition the phenotypic correlation between mates for a focal trait--the standard measure for assortative mating--into a direct component and additional indirect components. Indirect assortative mating occurs when a nonassorting trait is correlated within individuals to a directly assorting trait. Direct and indirect assortative mating is assessed for flowering phenology in Brassica rapa. The flowering time of pollen recipients (mothers) was strongly correlated (rho=0.67) to that of potential pollen donors (fathers). Similarly, recipients and donors were correlated for duration of their flowering periods (rho=0.32) and stem diameters (rho=0.52). A partitioning of between-mate correlations revealed direct assortative mating for flowering time and period duration. However, assortment for stem diameter is explained solely through its correlation to flowering time. Examination of standard quantitative genetic theory shows that indirect assortative mating inflates genetic variance in a focal trait and the genetic covariance between focal and phenotypically correlated traits.     

Rules for assortative mating in relation to selection for linear merit functions

Summary This study examined how assortative mating (without selection) based on linear combinations of two traits could be used to change genetic parameters so as to increase efficiency of selection. The efficiency of the Smith-Hazel index for improvement of multiple traits is a function of phenotypic and genetic variances and covariances, and of the relative economic values of the traits involved. Assortative mating is known to change genetic variances and covariances. Recursive formulae were derived to obtain these variances and covariances after t generations of assortative mating on linear combinations (mating rules) of phenotypic values for two traits, with a given correlation between mates. Selection efficiency after t generations of assortative mating without selection was expressed as a function of random mating genetic parameters, economic values, the mating rule, and the correlation between mates. Selection efficiency was maximized with respect to the coefficients in the mating rule. Because the objective function was nonlinear, a computer routine was used for maximizing it. Two cases were considered. When random mating heritabilities for the two traits were h _X ² =0.25 and h _Y ² =0.50, the genetic correlation r_XY=-0.60, and the economic values were a_X=3 and a_Y=1, continued assortative mating based on the optimal mating rule for 31 generations (with a correlation of 0.80 between mates) increased selection efficiency by 29%. Heritabilities changed to 0.38 and 0.66, respectively, and the genetic correlation became – 0.79. When h _X ² =0.60, h _Y ² =0.60, r_XY=– 0.20, a₁=1 and a₂=1, 36 generations of continued assortative mating with the optimal mating rule increased the efficiency of selection by 17%, heritabilities became h _X ² = h _Y ² =0.71, and the genetic correlation changed to 0.25. Only three generations of assortative mating were required to change the sign of the genetic correlation.     

Assortative mating for fitness and the evolution of recombination

To understand selection on recombination, we need to consider how linkage disequilibria develop and how recombination alters these disequilibria. Any factor that affects the development of disequilibria, including nonrandom mating, can potentially change selection on recombination. Assortative mating is known to affect linkage disequilibria but its effects on the evolution of recombination have not been previously studied. Given that assortative mating for fitness can arise indirectly via a number of biologically realistic scenarios, it is plausible that weak assortative mating occurs across a diverse set of taxa. Using a modifier model, we examine how assortative mating for fitness affects the evolution of recombination under two evolutionary scenarios: selective sweeps and mutation-selection balance. We find there is no net effect of assortative mating during a selective sweep. In contrast, assortative mating could have a large effect on recombination when deleterious alleles are maintained at mutation-selection balance but only if assortative mating is sufficiently strong. Upon considering reasonable values for the number of loci affecting fitness components, the strength of selection, and the mutation rate, we conclude that the correlation in fitness between mates is unlikely to be sufficiently high for assortative mating to affect the evolution of recombination in most species.     

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

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

Transfer systems and covariance under assortative mating

Summary This paper introduces the concept of a transfer system of random variables and uses it ot study various types of assortative mating. The standard correlation structure between relatives under phenotypic and genetic assortative mating are obtained easily and these results are then extended to multiple characters by means of multivariate transfer systems. Equilibrium values for the parameters are found and index assortative mating is considered with specific applications.     

Limits to the evolution of assortative mating by female choice under restricted gene flow

The evolution of assortative mating is a key component of the process of speciation with gene flow. Several recent theoretical studies have pointed out, however, that sexual selection which can result from assortative mating may cause it to plateau at an intermediate level; this is primarily owing to search costs of individuals with extreme phenotypes and to assortative preferences developed by individuals with intermediate phenotypes. I explore the limitations of assortative mating further by analysing a simple model in which these factors have been removed. Specifically, I use a haploid two-population model to ask whether the existence of assortative mating is sufficient to drive the further evolution of assortative mating. I find that a weakening in the effective strength of sexual selection with strong assortment leads to the existence of both a peak level of trait differentiation and the evolution of an intermediate level of assortative mating that will cause that peak. This result is robust to the inclusion of local adaptation and different genetic architecture of the trait. The results imply the existence of fundamental limits to the evolution of assortment via sexual selection in this situation, with which other factors, such as search costs, may interact.     

Pairing dynamics and the origin of species

Whether sexual selection alone can drive the evolution of assortative mating in the presence of gene flow is a long-standing question in evolutionary biology. Here, we report a role for pairing dynamics of individuals when mate choice is mutual, which is sufficient for the evolution of assortative mating by sexual selection alone in the presence of gene flow. Through behavioural observation, individual-based simulation and population genetic analysis, we evaluate the pairing dynamics of coral reef fish in the genus Hypoplectrus (Serranidae), and the role these dynamics can play for the evolution of assortative mating. When mate choice is mutual and the stability of mating pairs is critical for reproductive success, the evolution of assortative mating in the presence of gene flow is not only possible, but is also a robust evolutionary outcome.     

Assortative mating by size: A meta-analysis of mating patterns in water striders

Summary Assortative mating by size is a common mating pattern that can be generated by several different behavioural mechanisms, with different evolutionary implications. Assortative mating is typically associated with sexual selection and has been regarded as an attribute of populations, species, mating systems or even higher order taxa. In most animal groups, however, appropriate analyses of assortative mating at these different levels are lacking and the causes and forms of assortative mating are poorly understood. Here, we analyse 45 different population level estimates of assortative mating and non-random mating by size in seven confamiliar species of water striders that share a common mating system. A hierarchical comparative analysis shows that virtually all the variance within the clade occurs among samples within species. We then employ meta-analysis to estimate the overall strength of assortative mating, to determine the form of assortative mating and to further assess potential differences among species as well as the probable causes of assortative mating in this group of insects. We found overall weak but highly significant positive assortative mating. We show that analyses of the degree of heteroscedasticity in plots of male versus female size are critical, since the evolutionary implications of true and apparent assortative mating differ widely and conclude that the positive assortative mating observed in water striders was of the true rather than the apparent form. Further, within samples, mating individuals were significantly larger than non-mating individuals in both males and females. All of these non-random mating patterns were consistent among species and we conclude that weak positive assortative mating by size is a general characteristic of those water strider species that share this mating system. We use our results to illustrate the importance of distinguishing between different forms of assortative mating, to discriminate between various behavioural causes of assortative mating and to assess potential sources of interpopulational variance in estimates of assortative mating. Finally, we discuss the value of using meta-analytic techniques for detecting overall patterns in multiple studies of non-random mating.     

Morphological differentiation may mediate mate-choice between incipient species of Anopheles gambiae s.s

The M and S molecular forms of Anopheles gambiae s.s. have been considered incipient species for more than ten years, yet the mechanism underlying assortative mating of these incipient species has remained elusive. The discovery of the importance of harmonic convergence of wing beat frequency in mosquito mating and its relation to wing size have laid the foundation for exploring phenotypic divergence in wing size of wild populations of the two forms. In this study, wings from field collected mosquitoes were measured for wing length and wing width from two parts of the sympatric distribution, which differ with respect to the strength of assortative mating. In Mali, where assortative mating is strong, as evidenced by low rates of hybridization, mean wing lengths and wing widths were significantly larger than those from Guinea-Bissau. In addition, mean wing widths in Mali were significantly different between molecular forms. In Guinea-Bissau, assortative mating appears comparatively reduced and wing lengths and widths did not differ significantly between molecular forms. The data presented in this study support the hypothesis that wing beat frequency may mediate assortative mating in the incipient species of A. gambiae and represent the first documentation of a morphological difference between the M and S molecular forms.     

No evidence for size‐assortative mating in the wild despite mutual mate choice in sex‐role‐reversed pipefishes

Size‐assortative mating is a nonrandom association of body size between members of mating pairs and is expected to be common in species with mutual preferences for body size. In this study, we investigated whether there is direct evidence for size‐assortative mating in two species of pipefishes, Syngnathus floridae and S. typhle, that share the characteristics of male pregnancy, sex‐role reversal, and a polygynandrous mating system. We take advantage of microsatellite‐based “genetic‐capture” techniques to match wild‐caught females with female genotypes reconstructed from broods of pregnant males and use these data to explore patterns of size‐assortative mating in these species. We also develop a simulation model to explore how positive, negative, and antagonistic preferences of each sex for body size affect size‐assortative mating. Contrary to expectations, we were unable to find any evidence of size‐assortative mating in either species at different geographic locations or at different sampling times. Furthermore, two traits that potentially confer a fitness advantage in terms of reproductive success, female mating order and number of eggs transferred per female, do not affect pairing patterns in the wild. Results from model simulations demonstrate that strong mating preferences are unlikely to explain the observed patterns of mating in the studied populations. Our study shows that individual mating preferences, as ascertained by laboratory‐based mating trials, can be decoupled from realized patterns of mating in the wild, and therefore, field studies are also necessary to determine actual patterns of mate choice in nature. We conclude that this disconnect between preferences and assortative mating is likely due to ecological constraints and multiple mating that may limit mate choice in natural populations.     

Prediction of Response to Selection and Inbreeding Coefficient under Assortative Mating

A method for predicting response to selection and inbreeding coefficient under the continuous use of assortative mating was derived. Using the method, numerical computation was carried out, and the utility of assortative mating in the selection programmes was evaluated. It was shown that the continuous use of assortative mating could not produce an appreciable additional increase in intermediate- or long-term selection response.     

Assortive mating for personaltiy traits, educational level, religious affiliation, height, weight, adn body mass index in parents of Korean twin sample.

The degree of assortative mating for psychological and physical traits in Asian societies in relatively unknown. The present study examined assortative mating for educational level, personality traits, religious affiliation, height, weight, and body mass index in a korean sample. Age-adjusted spouse correlations were high for educational level (r = .63) and religious affiliation (r = .67), modest for most personality traits (rs = -.01 to .26), and trivial for height (r = .04), weight (r = .05)m and body mass index (r = .11). These results were remarkably similar to those found from the western samples. Implications of the present findings in behavior genetic studies and human mating patterns were briefly discussed.     

Assortative mating and offspring well-being: theory and empirical findings from a native Amazonian society in Bolivia

Mate choice matters for inclusive fitness, household economic efficiency, assimilation, stratification, and economic inequalities in society. In positive assortative mating, people pair with someone who resembles them along a trait, whereas in negative assortative mating, people pair with someone who differs from them along a trait. In industrial nations, people tend to follow positive assortative mating for fundamental demographic dimensions (e.g., age, schooling) and might practice negative assortative mating for economic outcomes (e.g., earnings). Research on assortative mating has focused on industrial nations, generally compared only one trait between couples, and paid scant attention to the effects of assortative mating for offspring well-being. If assortative mating enhances inclusive fitness, it might also enhance offspring well-being. Drawing on data from a farming–foraging society in the Bolivian Amazon (Tsimane') that practices preferential cross-cousin marriage, we (a) identify six parental traits (age, knowledge, wealth, schooling, height, and smiles) for which Tsimane' might practice assortative mating and (b) test the hypothesis that assortative mating enhances offspring well-being. Proxies for offspring well-being include height and school attainment. Tsimane' resemble people of industrial nations in practicing mostly positive assortative mating. Pairwise, mother–father and Pearson correlations of age, schooling, and earnings among Tsimane' resemble correlations of industrial nations. Correlation coefficients for the six parental traits were far higher than correlations that might happened just by chance. We found weak support for the hypothesis that assortative mating improves offspring well-being.     

FOUNDER-FLUSH SPECIATION IN DROSOPHILA PSEUDOOBSCURA: A LARGE-SCALE EXPERIMENT

A founder-flush-crash model of speciation has been proposed that may particularly apply to island and other colonizations. Previous laboratory experiments testing the model have given inconsistent results. We have conducted a large experiment with Drosophila pseudoobscura designed to meet the essential postulates of the model and to separately test some of the postulates. Forty-five experimental and 12 control populations have been studied during seven successive founder-flush-crash cycles, or about 50 generations. Sexual isolation tests yield significantly positive assortative mating in a few tests between pairs of experimental populations. Populations with fewer founders (N = 1 or 3) yield more significant instances of assortative mating than those with more founders (n = 5, 7, or 9), and this difference becomes statistically significant for pooled data. Only one of 15 population pairs tested three times (generations 25, 32, and 46) shows positive assortative mating in all three tests. No significant assortative mating occurs between control populations, including highly inbred ones. We conclude that although founder events may occasionally lead to the evolution of assortative mating and hence to speciation, our results do not support the claim that the founder-flush-crash model identifies conditions very likely to result in speciation events.