Environmental sex reversal,Trojan sex genes,and sex ratio adjustment: conditions and population consequences

The great diversity of sex determination mechanisms in animals and plants ranges from genetic sex determination (GSD, e.g. mammals, birds, and most dioecious plants) to environmental sex determination (ESD, e.g. many reptiles) and includes a mixture of both, for example when an individual’s genetically determined sex is environmentally reversed during ontogeny (ESR, environmental sex reversal, e.g. many fish and amphibia). ESD and ESR can lead to widely varying and unstable population sex ratios. Populations exposed to conditions such as endocrine‐active substances or temperature shifts may decline over time due to skewed sex ratios, a scenario that may become increasingly relevant with greater anthropogenic interference on watercourses. Continuous exposure of populations to factors causing ESR could lead to the extinction of genetic sex factors and may render a population dependent on the environmental factors that induce the sex change. However, ESR also presents opportunities for population management, especially if the Y or W chromosome is not, or not severely, degenerated. This seems to be the case in many amphibians and fish. Population growth or decline in such species can potentially be controlled through the introduction of so‐called Trojan sex genes carriers, individuals that possess sex chromosomes or genes opposite from what their phenotype predicts. Here, we review the conditions for ESR, its prevalence in natural populations, the resulting physiological and reproductive consequences, and how these may become instrumental for population management.     

Heritability of sex tendency in a harpacticoid copepod,Tigriopus californicus

Abstract.— Systems with genetic variation for the primary sex ratio are important for testing sex-ratio theory and for understanding how this variation is maintained. Evidence is presented for heritable variation of the primary sex ratio in the harpacticoid copepod Tigriopus californicus. Variation in the primary sex ratio among families cannot be accounted for by Mendelian segregation of sex chromosomes. The covariance in sex phenotype between full-sibling clutches and between mothers and offspring suggests that this variation has a polygenic basis. Averaged over four replicates, the full-sibling heritability of sex tendency is 0.13 ± 0.040; and the mother-offspring heritability of sex tendency is 0.31 ± 0.216. Genetic correlations in the sex phenotype across two temperature treatments indicate large genotype-by-temperature interactions. Future experiments need to distinguish between zygotic, parental, or cytoplasmic mechanisms of sex determination in T. californicus.     

Sex-Specific Territorial Behaviour in the Banggai Cardinalfish, Pterapogon kaunderni

In a field experiment, we studied how levels of aggression in males and females in established pairs of the Banggai cardinalfish were influenced by the sex of an experimentally introduced individual larger and more attractive than its resident counterpart. Contrary to previous studies on other cardinalfish species, and contrary to expectations in a sex role reversed species, the male was the main aggressor towards an intruder. Moreover, residents were more aggressive towards an intruder of the same sex as themselves. Furthermore, even though females often courted introduced, larger males, no intruder managed to take over the partnership of any resident. We suggest that our findings imply relatively equal sex roles in the Banggai cardinalfish and we discuss the evolution of sex specific territory defence and its significance in the Banggai cardinalfish as well as the implications of such behaviour in the interpretations of sex roles in general.     

Phylogeography,more than elevation,accounts for sex chromosome differentiation in Swiss populations of the common frog (Rana temporaria)*

Sex chromosomes in vertebrates range from highly heteromorphic (as in most birds and mammals) to strictly homomorphic (as in many fishes, amphibians, and nonavian reptiles). Reasons for these contrasted evolutionary trajectories remain unclear, but species such as common frogs with polymorphism in the extent of sex chromosome differentiation may potentially deliver important clues. By investigating 92 common frog populations from a wide range of elevations throughout Switzerland, we show that sex chromosome differentiation strongly correlates with alleles at the candidate sex-determining gene Dmrt1. Y-specific Dmrt1 haplotypes cluster into two main haplogroups, Y_A and Y_B, with a phylogeographic signal that parallels mtDNA haplotypes: Y_A populations, with mostly well-differentiated sex chromosomes, occur primarily south of the main alpine ridge that bisects Switzerland, whereas Y_B populations, with mostly undifferentiated (proto-)sex chromosomes, occur north of this ridge. Elevation has only a marginal effect, opposing previous suggestions of a major role for climate on sex chromosome differentiation. The Y-haplotype effect might result from differences in the penetrance of alleles at the sex-determining locus (such that sex reversal and ensuing X-Y recombination are more frequent in Y_B populations), and/or fixation of an inversion on Y_A (as supported by the empirical observation that Y_A haplotypes might not recombine in XY_A females).     

The variations of human sex ratio at birth with time of conception within the cycle, coital rate around the time of conception, duration of time taken to achieve conception, and duration of gestation: a synthesis

There is a large research literature on the variation of human sex ratio (proportion of males at birth) with (1) time of insemination within the mother's fruitful cycle (TWC), (2) duration of gestation (DOG), (3) coital frequency, here called ‘coital rate’ (CR) and (4) duration of time taken to achieve conception in a period of risk (viz. in the absence of birth limitation methods) (TTC). The variation of sex ratio with each of these four variables has usually been treated as a discrete topic. Consider the four propositions that each of these sorts of variation exists. Here it is argued that these propositions entail one another to varying degrees, and that, for that reason, empirical failures to detect (at conventional levels of significance) one such form of variation (as e.g. with time to conception) should not justify rejecting the hypothesis that such variation exists until the whole network of propositions has been considered. Evidence that offspring sex ratio varies with time of conception within the cycle is strong. It is argued here that, as a consequence, the available data constitute evidence that sex ratio varies with CR and with time to achieve conception, although this variation is small, difficult to detect and of no clinical significance. Lastly, sex ratio varies substantially with DOG, though the explanation for this is not established: it is suggested that the present treatment provides a testable framework for such an explanation.     

SEXUAL COMPOSITION and ANALYSIS OF REPRODUCTIVE FEMALES IN THE NORTH ATLANTIC RIGHT WHALE, EUBALAENA GLACIALIS, POPULATION

To test hypotheses involving reproduction and demographics, the sex of individuals must be established, but many species of Cetacea are not obviously dimorphic. In the North Atlantic right whale, Eubalaena glacialis , population, the sex of 61 males and 55 females had been determined previously by observation of the urogenital region, and the sex of 43 more females had been inferred from repeated sightings with a calf. To confirm the sex of some of these animals and to identify the sex of mote animals, genomic DNA was isolated from skin samples of 95 individual right whales (54 from among those described above and 41 additional recognizable individuals). The DNA was surveyed using the human Y-chromosome probe pDP1007. With Eco RI-digested DNA, a clear, sex-discriminating banding pattern was apparent. This method verified the sex of all 54 animals whose sex was previously known or inferred and identified the sex of an additional 41 recognizable individuals. A total of 89 male and 111 female right whales was identified in the population. The most unbiased estimate of sex ratio available is the 36 male and 34 female calves identified by genital morphology and DNA techniques. The sex ratio of this sample does not differ significantly from unity (P = 0.811). Only 38% (58/152) of the females in the North Atlantic population are known to have been reproductively successful compared with 54% in the population of right whales in the western South Atlantic. The population growth rate reported for the North Atlantic population is only 33% of that reported for right whales in the South Atlantic. Thirteen adult North Atlantic females have been identified that have not been known to calve during the past 11 yr. These data suggest that the absence of measurable recovery may be due to a combination of fewer actively reproducing females and lower reproductive rates of some females.     

Egg-laying, pre-imaginal growth dynamics, and mortality in Eupelmus orientalis and Dinarmus basalis, two solitary ectoparasitoids of Callosobruchus maculatus

In Eupelmus orientalis and Dinarmus basalis, two ectoparasitoid species of Callosobruchus maculatus larvae, pre-imaginal development occurs within a leguminous seed, and is then impossible to observe directly. Offspring sex ratio is normally determined when adults emerge, and mortality during pre-imaginal stages remains unknown. By using translucent gelatine capsules containing a host larva to mimic the seed, we conducted an experimental study of offspring production and sex ratio with measurements of growth and pre-imaginal mortality. Mated females were allowed to lay eggs on hosts in seeds or in gelatine capsules. In the gelatine capsules the parasitoid was observed daily and measured to assess if the offspring sex ratio can be determined before emergence of adults. When seeds are replaced with gelatine caps, the number of egg-laying females decreases (48% in Eupelmus orientalis and 72% in Dinarmus basalis of females ovipositing on seeds lay eggs on gelatine capsules), and the offspring output changes qualitatively in Eupelmus orientalis (egg numbers constant, sex ratio diminishing from 0.75 to 0.46) and quantitatively in Dinarmus basalis (egg numbers diminishing, sex ratio maintained about 0.7). In Eupelmus orientalis, pre-imaginal mortality occurs principally in the first three days, the critical stage is hatching, and the final mortality is 30.1%. In Dinarmus basalis, mortality of larvae increases gradually from the 2nd to the 7th day, the final mortality being 13.6%. (3) In both species sex of the offspring can be determined before emergence but only after most mortality has occurred.     

ZW,XY, and yet ZW: Sex chromosome evolution in snakes even more complicated

Snakes are historically important in the formulation of several central concepts on the evolution of sex chromosomes. For over 50 years, it was believed that all snakes shared the same ZZ/ZW sex chromosomes, which are homomorphic and poorly differentiated in “basal” snakes such as pythons and boas, while heteromorphic and well differentiated in “advanced” (caenophidian) snakes. Recent molecular studies revealed that differentiated sex chromosomes are indeed shared among all families of caenophidian snakes, but that boas and pythons evolved likely independently male heterogamety (XX/XY sex chromosomes). The historical report of heteromorphic ZZ/ZW sex chromosomes in a boid snake was previously regarded as ambiguous. In the current study, we document heteromorphic ZZ/ZW sex chromosomes in a boid snake. A comparative approach suggests that these heteromorphic sex chromosomes evolved very recently and that they are poorly differentiated at the sequence level. Interestingly, two snake lineages with confirmed male heterogamety possess homomorphic sex chromosomes, but heteromorphic sex chromosomes are present in both snake lineages with female heterogamety. We point out that this phenomenon is more common across squamates. The presence of female heterogamety in non‐caenophidian snakes indicates that the evolution of sex chromosomes in this lineage is much more complex than previously thought, making snakes an even better model system for the evolution of sex chromosomes.     

Co-occurrence of multiple, supposedly incompatible modes of sex determination in a lizard population

Sex is determined genetically in some species (genotypic sex determination, or GSD) and by the environment (environmental sex determination, or ESD) in others. The two systems are generally viewed as incompatible alternatives, but we have found that sex determination in a species of montane lizard ( Bassiana duperreyi , Scincidae) in south-eastern Australia is simultaneously affected by sex chromosomes and incubation temperatures, as well as being related to egg size. This species has strongly heteromorphic sex chromosomes, and yet incubation at thermal regimes characteristic of cool natural nests generates primarily male offspring. We infer that incubation temperatures can over-ride genetically determined sex in this species, providing a unique opportunity to explore these alternative sex-determining systems within a single population.     

Variation in Population and Life History Traits of the American Eel, Anguilla rostrata, in Four Rivers in Maine

We examined population traits of yellow American eels from nine sites with similar habitat characteristics in each of four rivers in Maine, U.S.A. Migrating silver eels were also collected to compare sex ratio, age and size at migration among the four rivers. Population density and biomass were not significantly different among rivers with mean ranges of 8.4–21.8 eels 100m^–2and 380–1485gm^–2. Pairwise comparisons of the slopes of weight–length relationships of log transformed data (pooled data: intercept = –6.007, slope = 3.094, r²= 0.99, and n = 3116) revealed no significant differences among rivers. Length–age relationships (pooled data: intercept = 87.826, slope = 23.444, r²= 0.76, and n = 2325) also showed no statistically significant pairwise differences in slopes among rivers. In all rivers, sexual differentiation was complete by 270mm total length and age eleven. The sex ratios of migrating silver eels were not correlated with yellow eel sex ratios among the four rivers. Mean age at migration among the four rivers was significantly different for males only, with a range of 1.3years. Both sexes had some significant differences in size at migration among rivers, but the biological importance of the differences is tenuous (male range: 15mm, female range: 36mm). The yellow and silver eel population traits from these four rivers showed little variation when riverine habitat was isolated. Variations in traits appeared to be greater when eels from non-riverine habitats may have been present.     

Sex ratio, sex-specific chick mortality and sexual size dimorphism in birds

It has been suggested that sexual size dimorphism (SSD) may influence sex ratios at different life stages. Higher energy requirements during growth associated with larger body size could lead to a greater mortality of the larger sex and ultimately to an overproduction of the smaller sex. To explore the associations between SSD and hatching and fledging sex ratio we performed a species-level analysis and a phylogenetically controlled analysis, based on 83 bird species. Overall, there was a significant inverse relationship between the degree of SSD and the proportion of males at hatching and fledging. Sex-specific mortality related to SSD showed a weak but persistent negative tendency, suggesting a mortality bias towards the larger sex. These results suggest that changes in relation to SSD may take place mainly at the conception stage, but could be adjusted during growth. However, conclusions should be treated cautiously as these relationships weaken when additional variables are considered.     

Observations on the sexual system and the natural history of the semi-terrestrial shrimp Merguia rhizophorae (Rathbun, 1900)

Abstract. The sexual system of the semi-terrestrial shrimp Merguia rhizophorae is described, along with natural history observations on this unusual caridean. Individuals of M. rhizophorae in the Bocas del Toro Archipelago, Panama, were found occupying fossilized coral terraces in the upper and mid-intertidal zones, inhabiting caves and crevices, in and out of water. These fossilized coral terraces represent a new habitat for this species, which was previously reported only from mangrove swamps. Males, which made up 65% of the studied population, were smaller than females on average. No small juvenile females were observed, but transitional individuals having the characteristics of both males (gonopores) and females (ovaries) were observed in the population. These data suggest that individuals of M. rhizophorae are protandric hermaphrodites. Logistic regression indicated that the carapace length at which 50% of the individuals change sex is 4.89 mm. The abundance of shrimps at the study site was low. Shrimps were usually solitary, but occasionally observed in groups of ≤5 individuals. Shrimps were commonly observed walking while out of water, and in some cases, emerged shrimps jumped vigorously, presumably to avoid capture by the researcher or by predatory crabs. Additional studies on the reproductive biology and the behavioral ecology of members of this genus and of members of the closely related families Barbouridae and Lysmatidae will aid in understanding the evolutionary origin and the adaptive value of gender expression patterns in shrimps.     

Anisogamy,sexual selection,and the evolution and maintenance of sex

Summary In the present paper we distinguish between two aspects of sexual reproduction. Genetic recombination is a universal features of the sexual process. It is a primitive condition found in simple, single-celled organisms, as well as in higher plants and animals. Its function is primarily to repair genetic damage and eliminate deleterious mutations. Recombination also produces new variation, however, and this can provide the basis for adaptive evolutionary change in spatially and temporally variable environments.The other feature usually associated with sexual reproduction, differentiated male and female roles, is a derived condition, largely restricted to complex, diploid, multicellular organisms. The evolution of anisogamous gametes (small, mobile male gametes containing only genetic material, and large, relatively immobile female gametes containing both genetic material and resources for the developing offspring) not only established the fundamental basis for maleness and femaleness, it also led to an asymmetry between the sexes in the allocation of resources to mating and offspring. Whereas females allocate their resources primarily to offspring, the existence of many male gametes for each female one results in sexual selection on males to allocate their resources to traits that enhance success in competition for fertilizations. A consequence of this reproductive competition, higher variance in male than female reproductive success, results in more intense selection on males.The greater response of males to both stabilizing and directional selection constitutes an evolutionary advantage of males that partially compensates for the cost of producing them. The increased fitness contributed by sexual selection on males will complement the advantages of genetic recombination for DNA repair and elimination of deleterious mutations in any outcrossing breeding system in which males contribute only genetic material to their offspring. Higher plants and animals tend to maintain sexual reproduction in part because of the enhanced fitness of offspring resulting from sexual selection at the level of individual organisms, and in part because of the superiority of sexual populations in competition with asexual clones.     

Coalescent Times and Patterns of Genetic Diversity in Species with Facultative Sex: Effects of Gene Conversion,Population Structure,and Heterogeneity

Many diploid organisms undergo facultative sexual reproduction. However, little is currently known concerning the distribution of neutral genetic variation among facultative sexual organisms except in very simple cases. Understanding this distribution is important when making inferences about rates of sexual reproduction, effective population size, and demographic history. Here we extend coalescent theory in diploids with facultative sex to consider gene conversion, selfing, population subdivision, and temporal and spatial heterogeneity in rates of sex. In addition to analytical results for two-sample coalescent times, we outline a coalescent algorithm that accommodates the complexities arising from partial sex; this algorithm can be used to generate multisample coalescent distributions. A key result is that when sex is rare, gene conversion becomes a significant force in reducing diversity within individuals. This can reduce genomic signatures of infrequent sex (i.e., elevated within-individual allelic sequence divergence) or entirely reverse the predicted patterns. These models offer improved methods for assessing null patterns of molecular variation in facultative sexual organisms.     

Evolution of habitat-dependent sex allocation in plants: superficially similar to, but intrinsically different from animals

Because pollen disperses and ovules do not, a basic difference in dispersal abilities of male and female gametes exists in plants. With an analytical model, we show that the combination of such sex-biased dispersal of gametes and variation of habitat quality results in two opposite selective forces acting on the evolution of sex allocation in plants: (i) a plant should overproduce pollen in good patches and overproduce ovules in poor patches in order to equilibrate secondary sex ratios of gametes after pollen dispersal; (ii) a plant should overproduce ovules in good patches and overproduce pollen in poor patches in order to increase the likelihood that its progeny establishes in good patches. Our theoretical results indicate that the evolution of habitat-dependent sex allocation should be favoured in plants, in a direction that depends on the relative dispersal ability of pollen and seeds. We also show that superficially similar predictions obtained for habitat-dependent evolutionarily stable sex allocation in animals actually result from a completely different balance between the two underlying evolutionary forces.     

Sex determination in fish: Lessons from the sex-determining gene of the teleost medaka, Oryzias latipes

Although sex determination systems in animals are diverse, sex-determining genes have been identified only in mammals and some invertebrates. Recently, DMY (DM domain gene on the Y chromosome) has been found in the sex-determining region on the Y chromosome of the teleost medaka fish, Oryzias latipes. Functional and expression analyses of DMY show it to be the leading candidate for the male-determining master gene of the medaka. Although some work is required to define DMY as the master sex-determining gene, medaka is expected to be a good experimental animal for investigating the precise mechanisms involved in primary sex determination in non-mammalian vertebrates. In this article, the process of identification of DMY and is summarized and the origins of DMY and sexual development of the medaka's gonads are reviewed. In addition, putative functions of DMY are discussed.     

Variable host quality, life-history invariants, and the reproductive strategy of a parasitoid wasp that produces single sex clutches

The parasitic wasp Achrysocharoides zwoelferi (Hymenoptera, Eulophidae) produces clutches consisting of only one sex. Moreover,male clutch size is invariably one while female clutches arein the range one to four. We designed field experiments todetermine the effect of host quality on clutch composition.We found that solitary male and solitary female clutches werereared from the same size mines, and that larger mines tendedto produce gregarious female clutches. A higher proportionof male clutches were placed in older hosts, despite theirlarge size. Variation in body size, both between and withinclutches, was measured in order to test the predictions of models that take into account the constraint that clutch size is aninteger trait, something of potential importance when absoluteclutch size is low. Our data supported several predictionsof these models, including the trade-off-invariant rule foroptimal offspring size developed by Charnov and Downhower.However, while most invertebrate clutch size models assume equal resource share among members of the same clutch, we found anincrease in inequality in larger clutches.     

Survival, growth and sex ratios of gynogenetic diploid honmoroko

Survival, growth and sex ratios of gynogenetic diploid honmoroko Gnathopogon caerulescens induced by blocking the release of the second polar body were examined. Mean survival of gynogenetic juveniles at 130 days after hatching was about 33% lower than that of the controls. No significant difference was seen in early growth between control and gynogenetic diploids. Standard length and body weight in six groups of gynogenetic progeny were significantly greater but in two groups were significantly smaller than in the controls. Although 69% of gynogenetic diploids had well-developed gonads, the remaining 30% had undeveloped gonads (small in size or thread-like), and those gonads were divided into four types. The mean proportion of females in the 10 gynogenetic groups was 87·2% which was significantly ( P <0·01) higher than in the controls (44·7%). Gynogenetic diploids included 3·0–35·3% males. Most of those males produced a high proportion of female progeny, but the proportion of male offspring varied widely. From these results, the sex determining mechanism in honmoroko was presumed to be female homogamety, but other factors resulted in the production of males.     

Chromosome-level genomes of two armyworms,Mythimna separata and Mythimna loreyi,provide insights into the biosynthesis and reception of sex pheromones

Mythimna separata and Mythimna loreyi are global pests of gramineous cereals, heavily controlled with synthetic insecticides. Here, we generated two high-quality chromosome-level genome assemblies for M. separata (688 Mb) and M. loreyi (683 Mb). Our analysis identified Z and W chromosomes, with few genes and abundant transposable elements (TEs) found on the W chromosome. We also observed a recent explosion of long interspersed nuclear elements (LINEs), which contributed to the larger genomes of Mythimna. The two armyworms diverged ~10.5 MYA, with only three chromosomes have intrachromosomal rearrangements. Additionally, we observed a tandem repeat expansion of α-amylase genes in Mythimna, which may promote the digestion of carbohydrates and exacerbate their damage to crops. Furthermore, we inferred the sex pheromone biosynthesis pathway for M. separata, M. loreyi and Spodoptera frugiperda. We discovered that M. loreyi and S. frugiperda synthesized the same major constituents of sex pheromones through different pathways. Specifically, the double bonds in the dominant sex pheromone components of S. frugiperda were generated by Δ9- and Δ11-desaturase, while they were generated by Δ11-desaturase and chain-shortening reactions in M. loreyi. We also identified pheromone receptor (PR) genes and inferred their corresponding components. These findings provide a better understanding of sex pheromone communication and promote the development of a new pest control strategy involving pheromone traps, which are more effective and environmentally friendly than current strategies.