Sexual conflict and speciation

We review the significance of two forms of sexual conflict (different evolutionary interests of the two sexes) for genetic differentiation of populations and the evolution of reproductive isolation. Conflicting selection on the alleles at a single locus can occur in males and females if the sexes have different optima for a trait, and there are pleiotropic genetic correlations between the sexes for it. There will then be selection for sex limitation and hence sexual dimorphism. This sex limitation could break down in hybrids and reduce their fitness. Pleiotropic genetic correlations between the sexes could also affect the likelihood of mating in interpopulation encounters. Conflict can also occur between (sex-limited) loci that determine behaviour in males and those that determine behaviour in females. Reproductive isolation may occur by rapid coevolution of male trait and female mating preference. This would tend to generate assortative mating on secondary contact, hence promoting speciation. Sexual conflict resulting from sensory exploitation, polyspermy and the cost of mating could result in high levels of interpopulation mating. If females evolve resistance to make pre- and postmating manipulation, males from one population could be more successful with females from the other, because females would have evolved resistance to their own (but not to the allopatric) males. Between-locus sexual conflict could also occur as a result of conflict between males and females of different populations over the production of unfit hybrids. We develop models which show that females are in general selected to resist such matings and males to persist, and this could have a bearing on both the initial level of interpopulation matings and the likelihood that reinforcement will occur. In effect, selection on males usually acts to promote gene flow and to restrict premating isolation, whereas selection on females usually acts in the reverse direction. We review theoretical models relevant to resolution of this conflict. The winning role depends on a balance between the 'value of winning' and 'power' (relating to contest or armament costs): the winning role is likely to correlate with high value of winning and low costs. Sperm-ovum (or sperm-female tract) conflicts (and their plant parallels) are likely to obey the same principles. Males may typically have higher values of winning, but it is difficult to quantify 'power', and females may often be able to resist mating more cheaply than males can force it. We tentatively predict that sexual conflict will typically result in a higher rate of speciation in 'female-win' clades, that females will be responsible for premating isolation through reinforcement, and that 'female-win' populations will be less genetically diverse.     

Parental investment, reproductive success and polygyny in the lapwing, Vanellus vanellus

We studied the consequences of monogamy and polygyny for male and female lapwings at a site in northern England between 1993 and 1995. Males and females differed in breeding behaviour, and thus the pattern of reproductive investment: males contributed less time than females to the care of their offspring and more time to mating behaviour. We argue that this has resulted from sexual selection. Reproductive behaviour was similar in monogamous and polygynous individuals of both sexes. Male mating success was related to territory size, with males on the largest territories gaining more females. Polygynous male lapwings reared on average between 58 and 100% more chicks each year than monogamous males because of fewer complete breeding failures; between-year return rates of males to the area were similar. This would result in a strong advantage in terms of lifetime reproductive success for polygynous male lapwings. The seasonal breeding success of polygynous females was marginally, but not significantly, lower than that of monogamous females. Between-year return rates of monogamous and polygynous females were similar. Copyright 1998 The Association for the Study of Animal Behaviour.     

Sexual selection by male choice in monogamous and polygynous human populations

The theoretical possibility of coevolution of a viability-reducing female physical trait and a male mating preference for that trait by Fisherian sexual selection in monogamous and polygynous populations is demonstrated using two-locus haploid models. It is assumed that there is dichotomous variation in male resources, resource-rich males have a wider choice among females than resource-poor males, and a female has greater reproductive success when mated with a resource-rich male than a resource-poor one. Under these assumptions, we find that sexual selection operates effectively when female reproductive success is strongly dependent on male resource, the proportion of females that mate with resource-rich males is neither small nor large, the degree of polygyny is low, and resources are inherited from father to son. We suggest that some human female physical traits may have evolved by sexual selection through male choice. The evolution of skin color by sexual selection is discussed as an example.     

Sexual selection as a side-effect of sexual conflict in the seaweed fly, Coelopa ursina (Diptera: Coelopidae)

The mating system of the seaweed fly involves a premating struggle. When mounted, females violently try to remove the male. In this study 48% of premating struggles resulted in successful rejection of the male, 46% in copulation and 6% were terminated by the male. Large males had a mating advantage. However, contrary to what would be predicted if this sexual selection occurred as a result of active female mate choice, we found a positive association between the duration of premating struggles and male size. A positive association was also found between the duration of premating struggles and male mating success, suggesting that large males may benefit through their superior ability to withstand female rejection. Large females rejected males more easily than small females, suggesting that the premating struggle has not evolved to allow mate assessment by females. We conclude that sexual selection is occurring as a side-effect of the female rejection response, which has probably evolved in order to avoid costs associated with copulation. Nevertheless, a sexual size dimorphism has evolved with males being larger and much more variable in size than females. (c) 1998 The Association for the Study of Animal Behaviour.     

Male-male and male-female aggression may influence mating associations in wild octopuses (Abdopus aculeatus).

Abdopus aculeatus engages in frequent aggression and copulation, exhibits male mate-choice, and employs multiple mating tactics. Here we draw upon established hypotheses to compare male–male aggression (MMA) and male–female aggression (MFA), as they relate to their mating behavior in the wild. When contesting for females, males appear to balance mate preference (resource value) with perceived chances of winning contests (resource holding potential). Although males spent more time mating with and contesting for large “Adjacent Guarded” females (those occupying a den within arm’s reach of a large “Adjacent Guarding” male), they exhibited higher rates of aggression over nonadjacent “Temporarily Guarded” females that may be more accessible. The major determinant of male?male aggressive success was size, and this factor may dictate the expression of conditional mating tactics in males. “Adjacent Guarding” males were the largest and most aggressively successful males, earning the most time copulating with females. They are considered to have the highest resource holding potential (RHP) in MMA. By contrast, in MFA, some larger individuals fled from smaller individuals, indicating that RHP appears to be a function of both size and sex in intersexual aggression. This result suggests variation in aggressiveness, or potential for severe injury—even sexual cannibalism during MFA. Male–female aggression may also be influenced by the sexual nonreceptivity of some individuals, or attempts by both sexes to increase foraging behavior by delaying mate-guarding activity. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Sex differences in parasite infections: patterns and processes

Sex differences in parasite infection rates, intensities, or population patterns are common in a wide range of taxa. These differences are usually attributed to 1 of 2 causes: (1) ecological (sociological in humans); and (2) physiological, usually hormonal in origin. Examples of the first cause include differential exposure to pathogens because of sex-specific behavior or morphology. The second cause may stem from the well-documented association between testosterone and the immune system; sexually mature male vertebrates are often more susceptible to infection and carry higher parasite burdens in the field. Although many researchers favor one explanation over the other, the requisite controlled experiments to rule out confounding variables are often neglected. We suggest that sex differences in disease have evolved just as sex differences in morphology and behavior, and are the result of selection acting differently on males and females. Research has often focused on proximate mechanistic explanations for the sex difference in infection rates, but it is equally important to understand the generality of the patterns in an evolutionary context. Because males potentially gain more than females by taking risks and engaging in competition, sexual selection pressure has shaped male behavior and appearance to maximize competitive ability and attractiveness. Many of the classic male attributes such as antlers on deer are testosterone-dependent, putting males in what appears to be a cruel bind: become vulnerable to disease by developing an attractive secondary sexual ornament, or risk lowered mating success by reducing it. A variety of hypotheses have been put forward to explain why males have not circumvented this dilemma. The mating system of the host species will influence the likelihood of sex differences in parasite infection, because males in monogamous species are subject to weaker sexual selection than males in polygynous species. Whether these evolutionary generalizations apply to invertebrates, which lack testosterone, remains to be seen.     

Multiple open forms of ribose-binding protein trace the path of its conformational change

Spawning success of males and its correlates were investigated in a natural colony of whitebelly damselfish, A. leucogaster (Pomacentridae), to explore the criteria that females use in choosing mates. The mating success of individual males was variable, with some males acquiring as few as 5000 eggs and others as many as 450 000 eggs during a breeding season. Male spawning success was not correlated with body size, territory size, nest site parameters or parental care behaviour. Egg hatching success was not related to either male size or egg clutch size, and all males were capable of rearing eggs to hatching. The temporal sequence of choices by females indicated non-independent choice by females, such that males chosen by females on the first spawn of the day were also chosen by females that spawned later in the day. Field observations indicated that, in the absence of male courtship, females preferentially visited males that had eggs in their nest site. Males that had recently mated were preferred by females over those males with either late-stage eggs or no eggs in the nest. This female preference did not appear to be related to increased paternal care or egg clutch survival. Given that the mating system is promiscuous and non-resource based, and that there appears to be little difference among males in body size, females may be mating non-independently by mimicking the choice of other females. Copyright 1998 The Association for the Study of Animal Behaviour Copyright 1998 The Association for the Study of Animal Behaviour.     

Female preference for fly song: playback experiments confirm the targets of sexual selection

The courtship song of Drosophila is thought to be involved in sexual selection and species recognition. Because of the mating system of flies, however, directly demonstrating that song influences female preference is difficult. The majority of previous studies have used an experimental design that potentially confounds male and female reactions to song. In D. montana, correlational evidence has suggested that males that produce short sound pulses consisting of a high number of sound cycles (i.e. a high carrier frequency) have a higher mating success than other males. In this study, we played synthetic song that varied in pulse length and carrier frequency to individual females in the laboratory, both alone and in the presence of mute males. We scored female preference via an acceptance posture, 'wing spreading', which the females of this species usually display prior to mounting by a male. Females responded to synthetic song in the absence of males. The presence of mute males significantly increased their overall responsiveness, but the relative effectiveness of the songs did not change, eliminating male reaction to song as a possible confounding factor in the results. The interaction between pulse length and carrier frequency determined the discrimination between song types, with females responding most readily to song consisting of short pulses with a high carrier frequency. Thus, direct examination of female preferences supports the previous studies of male mating success, and confirms female song preference as a likely determinant of male mating success. Copyright 1998 The Association for the Study of Animal Behaviour     

Non-genetic benefits of mate choice: fecundity enhancement and sexy sons

I compared reproductive success (lifetime number of fertilized eggs) as a function of mate choice among females of the stink bug, Nezara viridula L. (Hemiptera: Pentatomidae). 'Choosing' (C) females were placed with one of two males on alternate days. CI females chose between inexperienced males while CR females chose between males previously rejected by CI females. 'Non-choosing' (N) females were placed with the same male every day. Non-choosing NI, NR and NA females encountered, respectively, inexperienced males, previously rejected males, or previously accepted and mated males. Reproductive success was highest for CI females, showing direct selection on mate preferences. Reproductive success did not differ between CR and NR females, indicating that male quality, not the act of choosing a mate, affects fitness. CI females preferred males with longer antennae and their fecundity (lifetime number of eggs) was correlated with male antenna length, consistent with antenna length as an indicator of male ability to transfer nutritive sperm produced in paired harlequin lobes of the testes. Harlequin lobes were smaller in rejected than chosen males. In second-generation mate choice trials, sons of NR females competed well against sons of NA females but not against sons of CI females. This suggests that non-genetic paternal contributions that decline with prior mating account for the attractiveness of sons because sons of CI and NA females shared the same fathers. Sons experiencing mating success came from larger eggs and egg size was greatest for CI females, perhaps as a consequence of paternal nutritional contributions. Copyright 1998 The Association for the Study of Animal Behaviour. Copyright 1998 The Association for the Study of Animal Behaviour.     

Success breeds success in mating male reed frogs (Hyperolius marmoratus)

Studies of the distribution of mating success among males in frog choruses typically seek to identify specific phenotypic attributes that confer a higher mating success on certain individual males. These attributes invariably relate to competition among males: either direct competition in the form of aggression, or competition to attract and be chosen by females. In this paper, we present evidence that an additional factor may operate in frog choruses. We show that individual males who mate on a given night enjoy a higher probability of being successful on the next night, and we suggest that this is because successful mating enables males to conserve energy.     

Male traits, mating tactics and reproductive success in the buff-breasted sandpiper, Tryngites subruficollis

Buff-breasted sandpipers use a variety of mating tactics to acquire mates, including remaining at a single lek for most of the breeding season, attending multiple leks during the season, displaying solitarily or displaying both on leks and solitarily. We found that differences in body size, body condition, fluctuating asymmetry scores, wing coloration, territory location and behaviour (attraction, solicitation and agonistic) did not explain the observed variation in mating tactics used by males. Which males abandoned versus returned to leks was also not related to morphology or behaviour, and there was no tendency for males to join leks that were larger or smaller than the lek they abandoned. These results suggest that male desertion of leks was not dependent on a male's characteristics nor on the size of the lek he was presently attending. Males did join leks with larger males than their previous lek, perhaps to mate with females attracted to these larger 'hotshot' males. Males at both leks and solitary sites successfully mated. Lek tenure did not affect mating success, although lekking males appeared to mate more frequently than solitary males. Courtship disruption and to a lesser extent, female mimicry, were effective at preventing females from mating at leks, and may offer a partial explanation for female mating off leks. Our analysis that combined all males together within a year (regardless of mating tactic) indicated that males that attended leks for longer periods of time and that had fewer wing spots were significantly more likely to mate. Given some evidence that wing spotting declines with age, and that females inspect male underwings during courtship, the latter result suggests that female choice may play some role in determining male success. We suggest that male buff-breasted sandpipers may use alternative mating tactics more readily than males in other 'classic' lek-breeding species because: (1) unpredictable breeding conditions in this species' high arctic breeding range leads to low lek stability, which in turn hinders mate selection mechanisms mediated by male dominance and female choice; and (2) males are not constrained by morphological markings that indicate status or sex. Both characteristics may reduce the reproductive benefits associated with males adopting one mating tactic and result in a sort of scramble competition in which males switch between tactics as local conditions change.Copyright 1998 The Association for the Study of Animal Behaviour     

Mate choice and mate competition influence male body size in Japanese medaka

A sexual size dimorphism usually occurs when size-dependent reproductive advantages exist in only one sex. Studies on Japanese medaka, Oryzias latipes, have demonstrated reproductive size advantages in females but not in males, even though males and females are similar in body size. We conducted mate-choice and mate-copying tests in which a female could first associate with, then mate with, either a large (>/=1 sd+X standard length) or a small male (相似文献   

Retroviruses and sexual size dimorphism in domestic cats (Felis catus L.)

Hochberg and co-workers have predicted that an increase in host adult mortality due to parasites is balanced by an earlier age at first reproduction. In polygynous species we hypothesize that such a pattern would lead to diverging selection pressure on body size between sexes and increased sexual size dimorphism. In polygynous mammals, male body size is considered to be an important factor for reproductive success. Thus, under the pressure of a virulent infection, males should be selected for rapid growth and/or higher body size to be able to compete successfully as soon as possible with opponents. In contrast, under the same selection pressure, females should be selected for lighter adult body size or rapid growth to reach sexual maturity earlier. We investigated this hypothesis in the domestic cat Felis catus. Orange cats have greater body size dimorphism than non-orange cats. Orange females are lighter than non-orange females, and orange males are heavier than non-orange males. Here, we report the extent to which orange and non-orange individuals differ in infection prevelance for two retroviruses, feline immunodeficiency virus (FIV) and feline leukaemia virus (FeLV). FIV is thought to be transmitted almost exclusively through aggressive contacts between individuals, whereas FeLV transmission occurs mainly through social contacts. The pattern of infection of both diseases is consistent with the higher aggressiveness of orange cats. In both sexes, orange cats are significantly more infected by FIV, and tend to be less infected by FeLV than other cats. The pattern of infection is also consistent with an earlier age at first reproduction in orange than in non-orange cats, at least for females. These results suggest that microparasitism may have played an important role in the evolution of sexual size dimorphism of domestic cats.     

Genetic variability in sensitivity to population density affects the dynamics of simple ecological models

Many 1-dimensional discrete time ecological models contain a sensitivity parameter that does not affect the dynamic complexity of these models. We show that genetic variability in this parameter can have a strong effect on population dynamics. We incorporate ecological dynamics in two different population genetic models with one locus and two alleles. The first is the classical model of a randomly mating population in Hardy-Weinberg equilibrium, and the second is a model of differential selection in males and females. In populations in Hardy-Weinberg equilibrium, variability in the sensitivity parameter can be maintained by overdominance. In this case, the dynamics of the polymorphic population tend to be much simpler than those of monomorphic populations. In the model with different selection in males and females, polymorphisms can be maintained in various ways, e.g., by opposing directional selection in males and females. Polymorphism in the sensitivity parameter tends to simplify population dynamics in the model with different selection in males and females as well. A number of interesting dynamic effects can be observed, e.g., multiple attractors with complicated basins of attraction. Then the final state of the system after a successful invasion by mutant alleles may depend on the mutation rate and on the distribution of mutational steps. In addition, there are situations in which genetic variability destabilizes a stable population dynamic equilibrium in the monomorphic model. There is an analogy between genetic variability and variability imposed by the environment. If differences in sensitivity are caused by the environment, dynamic effects similar to those in the genetic models can be observed. In addition, source-sink structures that are known to occur in spatially structured models can be seen in the genetic model if one of the genotypes is inviable. The results suggest that combining ecological and population genetic models can lead to a number of new insights. More work is needed, e.g., with fertility models, in which fitnesses are not assigned to individuals, but to mating pairs.     

Individual variation in male vocal traits and female mating preferences in Bufo americanus

We investigated the amount of variation in mating behaviour between and within individual male and female American toads, because both sources of trait variation can influence the course of sexual selection. Males varied in all four call parameters investigated (dominant call frequency, pulse rate, call rate and call duration). Individual males lowered the dominant frequency of their call when they interacted vocally with nearby males. Dominant call frequency was more highly correlated with body size in vocally interacting males than in non-interacting males. Pulse rate of calls primarily varied with water temperature. Call rate and call duration showed the most variation of the four call properties, but this variation was unrelated to male morphology or social interactions. Females varied in three aspects of mating behaviour: two measures of pair formation and their preference for dominant frequency of male calls. The body size of paired males varied between females both in pairings initiated by either sex and in pairings initiated only by females. Males chosen by females were usually larger than average, although age and prior breeding experience of females did not affect mate choice. Playback experiments indicated that female preference for calls of low dominant frequency depended on the temporal patterning of alternative calls presented. Each of the four male vocal properties showed significant repeatability, but only one of the three aspects of female mating behaviour was repeatable. We discuss how different degrees of repeatability in sexual traits of males and females may influence the action and detection of sexual selection in this and other species. Copyright 1998 The Association for the Study of Animal Behaviour. Copyright 1998 The Association for the Study of Animal Behaviour.     

Polyandrous females discriminate against previous mates

In most animal species, particularly those in which females engage in polyandry, mate choice is a sequential process in which a female must choose to mate or not to mate with each male encountered. Although a number of theoretical and empirical investigations have examined the effects of sequential mate choice on the operation of sexual selection, how females respond to solicitation by previous mates has received little attention. Here, we report the results of a study carried out on the polyandrous pseudoscorpion, Cordylochernes scorpioides, that assessed the sexual receptivity of once-mated females presented after a lapse of 1.5 hr or 48 hr with either their first mate or a different male. Females exhibited a high level of receptivity to new males, irrespective of intermating interval. By contrast, time between matings exerted a strong effect on female receptivity to previous mates. After a lapse of 48 hr, females did not differ significantly in their receptivity toward previous mates and different males, whereas at 1.5 hr after first mating, females were almost invariably unreceptive to males from whom they had previously accepted sperm. This result could not be attributed to male size or mating experience or to male sexual receptivity. Indeed, males were as willing to transfer sperm to a previous mate as they were to a new female. This difference between males and females in their propensity to remate with the same individual may reflect a conflict between the sexes, with males seeking to minimize postcopulatory sexual selection and females actively keeping open the opportunity for sperm competition and female choice of sperm by discriminating against previous mates.     

Individual mating success, lek stability, and the neglected limitations of statistical power

The evolution of leks (aggregations of males displaying to females) cannot be explained solely by an increasing average gain in matings for each male as group size increases. This is because the mating skew, that is, the inequality among males in mating success, is often high and may vary with lek size. Here, we show that the common observation that matings become more evenly divided as lek size increases is also insufficient to explain by itself the benefits of aggregating. The benefits to individual males are highly sensitive to the exact relationship between mating skew and lek size, and very similar relationships can lead to opposite predictions concerning individual benefits. With data on published mating success for 18 species (71 leks), we show that different species have very similar skew versus lek size relationships. With current sample sizes, however, there is insufficient statistical power to distinguish between completely different alternatives concerning individual optima of males. Copyright 1998 The Association for the Study of Animal Behaviour     

Sex differences in mortality of people who visited emergency rooms for asthma and chronic obstructive pulmonary disease

We assess the sex differences in mortality in a population-based cohort of those Barcelona residents older than 14 yr of age who received emergency room services (ERS) for either chronic obstructive pulmonary disease (COPD) or asthma, during the period from 1985 to 1989. Vital status was followed to the end of 1995. A total of 15,517 individuals, 9,918 males and 5,599 females were included in the study. Asthma was diagnosed in 16% of males and 53% of females. Overall, 50% of males and 30% of females died during the follow-up period. The mortality rates in both males and females who visited emergency rooms for COPD or asthma were significantly higher than the expected rates in the general population. These relative increases in the mortality rates were significantly higher in females than in males for both causes of death, COPD (age-adjusted female/male ratio = 2.39), and asthma (ratio = 3.95). However, survival was better in females than males among individuals in the study. The higher fatality in males than females was observed for all causes of death, all respiratory causes, and COPD (risk ratio among patients with COPD = 0.42, 0.29-0.59, and among patients with asthma = 0.11, 0.02-0.60), but not for asthma. Mortality for asthma was higher in females with a diagnosis of COPD (2.79, 1.52-5.13), but it was not different among individuals in whom asthma was diagnosed (1.02, 0.56-1.87). Greater severity of COPD in males than in females could explain a higher risk of dying for all respiratory causes and COPD in males. The increased risk of asthma death in females may be due to problems of coding the term "asthma" in death certificates. The higher rates in females than in males when comparing with the general population, may be an expression of a greater similarity in risk factors, such as smoking, in our population than in males and females of the general population.     

Sex roles and sexual selection

Sexual selection has been portrayed as acting predominantly on males who compete with each other over copulatory access to females; selection was considered to be driven by females choosing between males at the pre- or postcopulatory level. However, a broader view of sexual selection is now emerging. Examining male discrimination between females and female-female competition has been beneficial in identifying factors influencing the direction and strength of sexual selection. Furthermore, consideration of processes such as sexual coercion or genetic incompatibility, which indirectly influence an individual's set of copulation partners, gamete set or their offspring success, has helped to clarify the ways in which sexual selection may operate. Moreover, there is increasing evidence that not all copulations translate directly to paternity and that paternity does not necessarily translate into successful offspring. Postcopulatory and postfertilization mechanisms that influence not only paternity share but offspring recruitment now require further consideration. The benefits to each sex of copulating with particular partners or with more than one partner remains an area of debate. More carefully designed studies which eliminate alternative possibilities or quantify the relative importance of different selective pressures will also benefit from considering that not all copulations function solely to inseminate or receive sperm. It is also now clear that not all individuals of one sex follow the same strategy. Examining the variation between individuals in reproductive behaviour, fertilization success and offspring success will be important in establishing the selective pressures and mechanisms underlying the operation of sexual selection. (c) 1998 The Association for the Study of Animal Behaviour.     

Age-specific inbreeding depression and components of genetic variance in relation to the evolution of senescence

Two major theories of the evolution of senescence (mutation accumulation and antagonistic pleiotropy) make different predictions about the relationships between age, inbreeding effects, and the magnitude of genetic variance components of life-history components. We show that, under mutation accumulation, inbreeding decline and three major components of genetic variance are expected to increase with age in randomly mating populations. Under the simplest version of the antagonistic pleiotropy model, no changes in the severity of inbreeding decline, dominance variance, or the genetic variance of chromosomal homozygotes are expected, but additive genetic variance may increase with age. Age-specific survival rates and mating success were measured on virgin males, using lines extracted from a population of Drosophila melanogaster. For both traits, inbreeding decline and several components of genetic variance increase with age. The results are consistent with the mutation accumulation model, but can only be explained by antagonistic pleiotropy if there is a general tendency for an increase with age in the size of allelic effects on these life-history traits.