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Operational Sex Ratio (operational + sex_ratio)

Distribution by Scientific Domains

Life Sciences	88%

Selected Abstracts

ADAPTATION TO EXPERIMENTAL ALTERATIONS OF THE OPERATIONAL SEX RATIO IN POPULATIONS OF DROSOPHILA MELANOGASTER

EVOLUTION, Issue 2 2008
Max Reuter
Theory predicts that males adapt to sperm competition by increasing their investment in testis mass to transfer larger ejaculates. Experimental and comparative data support this prediction. Nevertheless, the relative importance of sperm competition in testis size evolution remains elusive, because experiments vary only sperm competition whereas comparative approaches confound it with other variables, in particular male mating rate. We addressed the relative importance of sperm competition and male mating rate by taking an experimental evolution approach. We subjected populations of Drosophila melanogaster to sex ratios of 1:1, 4:1, and 10:1 (female:male). Female bias decreased sperm competition but increased male mating rate and sperm depletion. After 28 generations of evolution, males from the 10:1 treatment had larger testes than males from other treatments. Thus, testis size evolved in response to mating rate and sperm depletion, not sperm competition. Furthermore, our experiment demonstrated that drift associated with sex ratio distortion limits adaptation; testis size only evolved in populations in which the effect of sex ratio bias on the effective population size had been compensated by increasing the numerical size. We discuss these results with respect to reproductive evolution, genetic drift in natural and experimental populations, and consequences of natural sex ratio distortion. [source]

PERSPECTIVE: FEMALE REMATING, OPERATIONAL SEX RATIO, AND THE ARENA OF SEXUAL SELECTION IN DROSOPHILA SPECIES

EVOLUTION, Issue 9 2002
Therese Ann Markow
Abstract., As commonly observed among closely related species within a variety of taxa, Drosophila species differ considerably in whether they exhibit sexual dimorphism in coloration or morphology. Those Drosophila species in which male external sexual characters are minimal or absent tend, instead, to have exaggerated ejaculate traits such as sperm gigantism or seminal nutrient donations. Underlying explanations for the interspecific differences in the presence of external morphological sexual dimorphism versus exaggerated ejaculate traits are addressed here by examining the opportunity for sexual selection on males to occur before versus after mating in 21 species of Drosophila. Female remating frequency, an important component of the operational sex ratio, differs widely among Drosophila species and appears to dictate whether the arena of sexual selection is prior to, as opposed to after, copulation. Infrequent female mating results in fewer mating opportunities for males and thus stronger competition for receptive females that favors the evolution of male characters that maximize mating success. On the other hand, rapid female remating results in overlapping ejaculates in the female reproductive tract, such that ejaculate traits which enhance fertilization success are favored. The strong association between female remating frequency in a given species and the presence of sexually selected external versus internal male characters indicates that the relationship be examined in other taxa as well. [source]

Operational Sex Ratio and Alternative Reproductive Behaviours in Chinese Bushcricket, Gampsocleis gratiosa

ETHOLOGY, Issue 4 2006
Yong Gao
The effects of operational sex ratio (OSR) on male mating tactics in the Chinese bushcricket Gampsocleis gratiosa were investigated in male- and female-biased environments. We measured fresh and dry spermatophore contents and copulation duration, and counted sperm numbers of each copulation. The fresh weight of spermatophore and spermatophylax was positively correlated with male body weight. The males in a strongly male-biased environment produced significantly heavier fresh ampulla and more sperm per ejaculation, which were likely tactics for successful matings under the competition of rivals. The spermatophore might function as a structure to protect the fertilization potential of the ejaculate from rival males. [source]

Operational sex ratio, sexual conflict and the intensity of sexual selection

ECOLOGY LETTERS, Issue 5 2008
Patrick S. Fitze
Abstract Modern sexual selection theory indicates that reproductive costs rather than the operational sex ratio predict the intensity of sexual selection. We investigated sexual selection in the polygynandrous common lizard Lacerta vivipara. This species shows male aggression, causing high mating costs for females when adult sex ratios (ASR) are male-biased. We manipulated ASR in 12 experimental populations and quantified the intensity of sexual selection based on the relationship between reproductive success and body size. In sharp contrast to classical sexual selection theory predictions, positive directional sexual selection on male size was stronger and positive directional selection on female size weaker in female-biased populations than in male-biased populations. Thus, consistent with modern theory, directional sexual selection on male size was weaker in populations with higher female mating costs. This suggests that the costs of breeding, but not the operational sex ratio, correctly predicted the strength of sexual selection. [source]

Operational Sex Ratio and Alternative Reproductive Behaviours in Chinese Bushcricket, Gampsocleis gratiosa

PERSPECTIVE: FEMALE REMATING, OPERATIONAL SEX RATIO, AND THE ARENA OF SEXUAL SELECTION IN DROSOPHILA SPECIES

The mismeasurement of sexual selection

JOURNAL OF EVOLUTIONARY BIOLOGY, Issue 3 2010
H. KLUG
Abstract Sexual selection can explain major micro- and macro-evolutionary patterns. Much of current theory predicts that the strength of sexual selection (i) is driven by the relative abundance of males and females prepared to mate (i.e. the operational sex ratio, OSR) and (ii) can be generally estimated by calculating intra-sexual variation in mating success (e.g. the opportunity for sexual selection, Is). Here, we demonstrate the problematic nature of these predictions. The OSR and Is only accurately predict sexual selection under a limited set of circumstances, and more specifically, only when mate monopolization is extremely strong. If mate monopolization is not strong, using OSR or Is as proxies or measures of sexual selection is expected to produce spurious results that lead to the false conclusion that sexual selection is strong when it is actually weak. These findings call into question the validity of empirical conclusions based on these measures of sexual selection. [source]

Parental investment, sexual selection and sex ratios

JOURNAL OF EVOLUTIONARY BIOLOGY, Issue 4 2008
HANNA KOKKO
Abstract Conventional sex roles imply caring females and competitive males. The evolution of sex role divergence is widely attributed to anisogamy initiating a self-reinforcing process. The initial asymmetry in pre-mating parental investment (eggs vs. sperm) is assumed to promote even greater divergence in post-mating parental investment (parental care). But do we really understand the process? Trivers [Sexual Selection and the Descent of Man 1871,1971 (1972), Aldine Press, Chicago] introduced two arguments with a female and male perspective on whether to care for offspring that try to link pre-mating and post-mating investment. Here we review their merits and subsequent theoretical developments. The first argument is that females are more committed than males to providing care because they stand to lose a greater initial investment. This, however, commits the ,Concorde Fallacy' as optimal decisions should depend on future pay-offs not past costs. Although the argument can be rephrased in terms of residual reproductive value when past investment affects future pay-offs, it remains weak. The factors likely to change future pay-offs seem to work against females providing more care than males. The second argument takes the reasonable premise that anisogamy produces a male-biased operational sex ratio (OSR) leading to males competing for mates. Male care is then predicted to be less likely to evolve as it consumes resources that could otherwise be used to increase competitiveness. However, given each offspring has precisely two genetic parents (the Fisher condition), a biased OSR generates frequency-dependent selection, analogous to Fisherian sex ratio selection, that favours increased parental investment by whichever sex faces more intense competition. Sex role divergence is therefore still an evolutionary conundrum. Here we review some possible solutions. Factors that promote conventional sex roles are sexual selection on males (but non-random variance in male mating success must be high to override the Fisher condition), loss of paternity because of female multiple mating or group spawning and patterns of mortality that generate female-biased adult sex ratios (ASR). We present an integrative model that shows how these factors interact to generate sex roles. We emphasize the need to distinguish between the ASR and the operational sex ratio (OSR). If mortality is higher when caring than competing this diminishes the likelihood of sex role divergence because this strongly limits the mating success of the earlier deserting sex. We illustrate this in a model where a change in relative mortality rates while caring and competing generates a shift from a mammalian type breeding system (female-only care, male-biased OSR and female-biased ASR) to an avian type system (biparental care and a male-biased OSR and ASR). [source]

The effect of nest aggregation on the reproductive behaviour of the peacock blenny Salaria pavo

JOURNAL OF FISH BIOLOGY, Issue 4 2009
J. L. Saraiva
The effect of nest aggregation in courtship behaviour was tested experimentally in an ecologically constrained, sex-role reversed population of the peacock blenny Salaria pavo. Mixed sex groups of eight males and eight females were tested in experimental tanks, containing eight potential nests either aggregated or dispersed. In the aggregated treatment, males spent more time inside their nests and monopolized other potential nests, causing a female-biased operational sex ratio (OSR). In the aggregated treatment, females also expressed more courtship behaviour. The results in general support the prediction that the aggregation of nests promotes male monopolization of potential nests, resulting in fewer nest-holding males and therefore a female-biased OSR that leads to the reversal of sex roles. [source]

Yellow belly as honest signal of female quality in Knipowitschia panizzae(Gobiidae)

JOURNAL OF FISH BIOLOGY, Issue 2003
C. Mazzoldi
Sexually dimorphic traits are common in fish species, and examples from both males and females have been described. The function of these traits has been widely investigated in males. On the contrary, female ornaments have been studied mainly in sex role reversed species, such as pipefish, while their role in species with ,conventional' sex roles remain to be investigated. This study focused on the presence, function, and possible role as indicator of female quality of a sexually dimorphic nuptial trait in the lagoon goby, Knipowitschia panizzae. In this species, that present conventional sex roles, females show a yellow spot on the belly. Aquarium spawning experiments demonstrated that the coloration on the belly is due to dermal pigments, is displayed only when female is ready to spawn and is switched off within few minutes from the end of egg deposition. This sexual trait presents variability in size among females and indicates female fecundity relatively to her own body size. As a consequence, female yellow belly appears to be an honest signal of female quality. Field data on natural nests highlighted that males perform parental cares mostly only on one egg batch at a time and the modality of egg deposition suggested that males are limited in their potential reproductive rates by environmental factors. Male limitation in egg care could constitute the basis for a female biased operational sex ratio, favouring male choosiness and the evolution of female nuptial displays. [source]

Male mating tactics in spider monkeys: sneaking to compete

AMERICAN JOURNAL OF PRIMATOLOGY, Issue 9 2010
K. Nicole Gibson
Abstract I investigated the mating system and male mating tactics for a population of wild spider monkeys (Ateles belzebuth chamek), to identify the behaviors males used to achieve and maintain access to sexually receptive females, and to examine if some males used more tactics than other males and/or had differential access to females. Results show that the mating system mostly involved scramble competition polygyny and that males used a range of mating tactics and behaviors, previously unreported for spider monkeys. The most unusual feature of spider monkey mating behavior was the secretive nature of copulations,nearly all copulations were clandestine, but a few were in the presence of other group members. Fifteen sexually mature males were observed to copulate 43 times. These data provide the first opportunity to evaluate how female availability influences male,male competition. First, the operational sex ratio was highly skewed toward males because usually only one female was receptive in each community per month. Second, females only mated with a few males in their community in any one mating period, but some females mated over the course of multiple consecutive mating periods, eventually mating with most or all of the males in their community. Across all communities, 9 (21%) of the 43 copulations involved a single male,female partner, 20 (47%) involved four males mating with the same female, and males mated with from one to four different females. Fourteen of the 16 total adult males and 1 subadult male (10 total) copulated. One or two males in each community were successful in monopolizing access to receptive females, and these males did not usually have the highest rates of copulation. In this system, clandestine copulations are one behavioral solution to the complex problem of gaining mating exclusivity and, probably, exercising mate choice. Am. J. Primatol. 72:794,804, 2010. © 2010 Wiley-Liss, Inc. [source]

Guppies control offspring size at birth in response to differences in population sex ratio

BIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 2 2010
MIGUEL BARBOSA
Females that invest adaptively in their offspring are predicted to channel more resources to the sex that will be at an advantage in the prevailing environmental conditions. Here, we report, for the first time, that female Trinidadian guppy, Poecilia reticulata, respond in reproductively distinct ways when faced with differences in operational sex ratio. We show that females assigned to a female-biased sex ratio produce larger male offspring than females in an environment in which males predominate. Given the link between size at birth and fitness, and the marked reproductive skew in this species, larger male offspring are expected to have reproductive advantages in guppy populations with an excess of females. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 100, 414,419. [source]

Female polymorphism, condition differences, and variation in male harassment and ambient temperature

BIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 3 2009
JESSICA BOTS
Female polymorphism is considered to be maintained through negative frequency-dependent selection imposed by costly male harassment. However, few studies have questioned whether male harassment negatively affects female morph success and does so differently for female morphs, especially in the wild. In the present study, we quantified female morph condition (relative body mass and energy reserves) for a colour polymorphic damselfly under natural conditions and evaluated these measures against variation in proxies of male harassment (population density and operational sex ratio) and ambient temperature. Differences in protein content between female morphs were detected and the variation in condition could partly be explained from concomitant variation in proxies of male harassment. Specifically, the relationship between protein content and operational sex ratio differed between morphs in that the negative effect of male harassment was more pronounced in gynomorphs than in andromorphs. In addition, ambient temperature affected the body mass and protein content of female morphs differently, with andromorphs having higher condition values in favourable weather conditions, whereas, for gynomorphs, the patterns tended to be opposite. In conclusion, the results obtained in the present study suggest that male harassment negatively and differentially affects female morph success. Future studies should aim to elucidate whether the observed effects of ambient temperature contribute to the maintenance of the polymorphism. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 97, 545,554. [source]

The evolution of male mate choice in insects: a synthesis of ideas and evidence

BIOLOGICAL REVIEWS, Issue 3 2001
RUSSELL BONDURIANSKY
ABSTRACT Mate choice by males has been recognized at least since Darwin's time, but its phylogenetic distribution and effect on the evolution of female phenotypes remain poorly known. Moreover, the relative importance of factors thought to underlie the evolution of male mate choice (especially parental investment and mate quality variance) is still unresolved. Here I synthesize the empirical evidence and theory pertaining to the evolution of male mate choice and sex role reversal in insects, and examine the potential for male mating p to generate sexual selection on female phenotypes. Although male mate choice has received relatively little empirical study, the available evidence suggests that it is widespread among insects (and other animals). In addition to ,precopulatory' male mate choice, some insects exhibit ,cryptic' male mate choice, varying the amount of resources allocated to mating on the basis of female mate quality. As predicted by theory, the most commonly observed male mating p are those that tend to maximize a male's expected fertilization success from each mating. Such p tend to favour female phenotypes associated with high fecundity or reduced sperm competition intensity. Among insect species there is wide variation in mechanisms used by males to assess female mate quality, some of which (e.g. probing, antennating or repeatedly mounting the female) may be difficult to distinguish from copulatory courtship. According to theory, selection for male choosiness is an increasing function of mate quality variance and those reproductive costs that reduce, with each mating, the number of subsequent matings that a male can perform (,mating investment'). Conversely, choosiness is constrained by the costs of mate search and assessment, in combination with the accuracy of assessment of potential mates and of the distribution of mate qualities. Stronger selection for male choosiness may also be expected in systems where female fitness increases with each copulation than in systems where female fitness peaks at a small number of matings. This theoretical framework is consistent with most of the empirical evidence. Furthermore, a variety of observed male mating p have the potential to exert sexual selection on female phenotypes. However, because male insects typically choose females based on phenotypic indicators of fecundity such as body size, and these are usually amenable to direct visual or tactile assessment, male mate choice often tends to reinforce stronger vectors of fecundity or viability selection, and seldom results in the evolution of female display traits. Research on orthopterans has shown that complete sex role reversal (i.e. males choosy, females competitive) can occur when male parental investment limits female fecundity and reduces the potential rate of reproduction of males sufficiently to produce a female-biased operational sex ratio. By contrast, many systems exhibiting partial sex role reversal (i.e. males choosy and competitive) are not associated with elevated levels of male parental investment, reduced male reproductive rates, or reduced male bias in the operational sex ratio. Instead, large female mate quality variance resulting from factors such as strong last-male sperm precedence or large variance in female fecundity may select for both male choosiness and competitiveness in such systems. Thus, partial and complete sex role reversal do not merely represent different points along a continuum of increasing male parental investment, but may evolve via different evolutionary pathways. [source]