Home About us Contact
|
Home About us Contact | ||
|
|
||
Conventional Sex Roles (conventional + sex_role)
Selected AbstractsParental investment, sexual selection and sex ratiosJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 4 2008HANNA 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] Yellow belly as honest signal of female quality in Knipowitschia panizzae(Gobiidae)JOURNAL OF FISH BIOLOGY, Issue 2003C. 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] Genetic monogamy despite social promiscuity in the pot-bellied seahorse (Hippocampus abdominalis)MOLECULAR ECOLOGY, Issue 11 2007A. B. WILSON Abstract Sexual selection theory predicts a positive correlation between relative parental investment and mate choice. In syngnathid fishes (seahorses and pipefish), males brood offspring in specialized brooding structures. While female-female mating competition has been demonstrated in some pipefishes, all seahorses (genus Hippocampus) studied to date have been found to have conventional sex roles with greater male,male competition for access to mates despite possessing the most complex brood structures in the family. Although multiple mating is common in pipefish, seahorses are again exceptional, exhibiting strict genetic monogamy. Both demographic and behavioural explanations have been offered to explain the lack of multiple mating in seahorse species, but these hypotheses have not yet been explicitly addressed. We investigated mating systems and brood parentage of the pot-bellied seahorse, Hippocampus abdominalis, a temperate-water species that is socially promiscuous with conventional sex roles in laboratory populations. We observed promiscuous courtship behaviour and sex-role reversal in high density, female-biased field populations of H. abdominalis. We hypothesize that sex roles are plastic in H. abdominalis, depending on local population density and sex ratio. Despite promiscuous courtship behaviour, all assayed male seahorses were genetically monogamous in both laboratory and wild populations. Physiological limitations associated with embryo incubation may explain the absence of multiple mating in seahorses and may have played an important role in the development of the unique reproductive behaviour typical in these species. [source] Yellow belly as honest signal of female quality in Knipowitschia panizzae(Gobiidae)JOURNAL OF FISH BIOLOGY, Issue 2003C. 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] | ||||||||||