Is there a relationship between sex of cystic fibrosis carriers and sex ratio of their offspring?

Summary Data on the offspring of 198 aunts and 179 uncles of 100 cystic fibrosis index cases were analyzed. Aunts showed higher average number of liveborn sons than uncles. No significant difference was observed in the number of liveborn female offspring. When the sample was subdivided with respect to family size, the proportion of liveborn sons of aunts appeared higher than that of uncles in all classes.The present observations suggest that a female carrier may have a higher probability of male offspring than a male carrier and that she may be mainly responsible for the sex ratio deviations previously reported in sibships of cystic fibrosis patients.     

Is Canada's sex ratio in decline?

In this issue (see pages 37 to 41) Dr. Bruce B. Allan and associates report a small but statistically significant decrease--of about 0.2%--in the proportion of male live births in Canada over the period 1970-90. In this editorial, factors that have been reported in the literature to influence sex ratio are examined within a Canadian context. The authors suggest that although the reasons for the apparent decline in the sex ratio in Canada are unclear, the increasing use of ovulation induction may be a contributing factor. Data from the Nova Scotia Atlee Perinatal Database are discussed with a view to explaining the trend observed in Atlantic Canada, but no obvious explanation emerges. The authors argue that when the period of observation is extended no overall change in the sex ratio is apparent. This would suggest a tendency toward stabilization rather than decline.     

The effect of temperature on sex ratio in the isopod Porcellionides pruinosus: Environmental sex determination or a by-product of cytoplasmic sex determination?

The sex ratios of the progenies of woodlice Porcellionides pruinosus (Crustacea, Isopoda) raised at different temperatures were studied. Females from three French populations sampled in the wild produced highly female-biased broods at 20°C and male-biased broods above 30°C. The effect of high temperature was not due to selective mortality of females. Sex determination was thus sensitive to temperature in P. pruinosus. We also found an interpopulation variability of sex ratio thermosensitivity and a weak inheritance of male-biased sex ratios at high temperatures. Samples taken from a wild population throughout the year showed that while the thermal conditions required for changes in the sex ratio occurred, there was no significant variation in the sex ratio. On the other hand, almost all the females and many males in the four populations studied harboured intracytoplasmic bacteria. These maternally inherited symbionts belong to the genus Wolbachia and are known to possess a feminizing effect. While in other arthropods Wolbachia are destroyed at high temperatures, the symbionts of P. pruinosus were detected by a PCR procedure whatever the rearing temperatures. In light of these results, we propose that the thermosensitivity of sex determination in P. pruinosus could reflect the removal of the cytoplasmic effect on sex determination rather than environmental sex determination sensu stricto. The reduction in the amount of bacteria (but not their entire elimination), or the inhibition of bacterial metabolism, may be responsible for sex ratio variations relating to temperature. The incomplete inheritance of male-biased sex ratios at high temperatures might reflect a selection of thermo-tolerant bacterial strains.     

Facultative primary sex ratio variation: a lack of evidence in birds?

The facultative control of primary sex ratio by breeding birds has become a major focus in evolutionary biology in recent years. A combination of well-developed theoretical literature and rapid publication of empirical results has created considerable confusion, with controversial claims for both extreme control of primary sex ratio versus no control around inherent random variability. We present a robust and quantitative summary of published empirical literature to assess clearly the body of evidence for female birds to control sex assignment in their offspring. Our meta-analytical approach reveals that published studies do not exhibit any variability beyond that which could be expected owing to sampling error. Therefore, we conclude that facultative control of offspring sex is not a characteristic biological phenomenon in breeding birds.     

Does polyandry control population sex ratio via regulation of a selfish gene?

The extent of female multiple mating (polyandry) can strongly impact on the intensity of sexual selection, sexual conflict, and the evolution of cooperation and sociality. More subtly, polyandry may protect populations against intragenomic conflicts that result from the invasion of deleterious selfish genetic elements (SGEs). SGEs commonly impair sperm production, and so are likely to be unsuccessful in sperm competition, potentially reducing their transmission in polyandrous populations. Here, we test this prediction in nature. We demonstrate a heritable latitudinal cline in the degree of polyandry in the fruitfly Drosophila pseudoobscura across the USA, with northern population females remating more frequently in both the field and the laboratory. High remating was associated with low frequency of a sex-ratio-distorting meiotic driver in natural populations. In the laboratory, polyandry directly controls the frequency of the driver by undermining its transmission. Hence we suggest that the cline in polyandry represents an important contributor to the cline in sex ratio in nature. Furthermore, as the meiotic driver causes sex ratio bias, variation in polyandry may ultimately determine population sex ratio across the USA, a dramatic impact of female mating decisions. As SGEs are ubiquitous it is likely that the reduction of intragenomic conflict by polyandry is widespread.     

Can the meiotic sex ratio explain the sex ratio bias in adult populations in the dioicous moss Drepanocladus lycopodioides?

Sex ratio variation is commonly observed in natural populations of many organisms with separate sexes and genetic sex determination, including bryophytes. Most bryophyte populations exhibit female-skewed expressed adult sex ratios, generally inferred from counts of sexually mature plants. For the rarely sexually reproducing perennial dioicous moss Drepanocladus lycopodioides, we showed that a female bias also exists in the genetic adult sex ratio, using a specifically designed molecular sex-associated marker. Here, we investigated whether the meiotic spore sex ratio contributes to the observed bias in genetic adult sex ratio in natural populations. Earlier attempts to study meiotic sex ratios have involved commonly cultivated ruderals that rapidly express sex in the laboratory. We established single-spore cultures from field-collected sporophytes from these populations and used the marker to assess the sex of individual sporelings. Spore germinability was (near) complete, and mortality among sporelings was virtually absent. The true meiotic sex ratio did not differ from equality, but strongly differed both from the observed genetic sex ratios in the natural adult populations, and from the European scale genetic sex ratio. We conclude that the biased population sex ratios in this species arise at life cycle stages after spore germination. Sexual dimorphism may selectively favour female proliferation during some phase of gametophyte development. Based on methodological progress, we successfully used a perennial study species with rare sexual reproduction, which significantly broadens the life history spectrum investigated in bryophyte sex ratio studies.     

Spiroplasma taxonomy and identification of the sex ratio organisms: can they be cultivated?

The spiroplasmas that occur naturally in several species of Drosophila were the first spiroplasmas ever observed, even though their discoverers, D.F. Poulson and B. Sakaguchi, in 1961 described them as being "treponema-like spirochetes." These Drosophila spiroplasmas are transovarially, or maternally, transmitted by infected females whose progenies are composed entirely of females. A more recently discovered Drosophila spiroplasma found in flies originating in Ito, Japan, is also maternally inherited but does not result in the elimination of males from the progeny of infected females. In spite of their early discovery, their high numerical density in the hemolymph of infected females (10(6)-10(7)/microliters), and numerous attempts at in vitro cultivation, they remain prime examples of non-cultivable spiroplasmas. It is the purpose of this paper to recount some of the approaches used in attempts at their cultivation.     

Is sexual dimorphism affected by the combined action of prenatal stress and sex ratio?

During embryonic development, offspring are exposed to hormones of both maternal and sibling origin. Maternal stress increases offspring exposure to corticosterone, and, in polytocous animals, the sex ratio or intrauterine position can influence the levels of androgens and estrogens experienced by the offspring. Such hormone exposure has the potential to influence many important morphological and behavioural aspects of offspring, in particular sexually dimorphic traits. Although well known in rodents, the impact of prenatal hormone exposure in other vertebrates is poorly documented. We experimentally investigated the relationship between maternal stress, population density, sex ratio (a surrogate for the degree of exposure to steroids produced by siblings), and sexual dimorphism in a viviparous lizard, Lacerta vivipara. Our results show that prenatal sex ratios have consequences for sexually dimorphic morphology (ventral scale count) in both sexes, but with no effect of maternal stress or any interaction between the two. Embryonic steroid exposure can potentially be an important factor in generating individual variation in natural populations of viviparous animals.     

Does operational sex ratio influence relative strength of purging selection in males versus females?

According to theory, sexual selection in males may efficiently purge mutation load of sexual populations, reducing or fully compensating ‘the cost of males’. For this to occur, mutations not only need to be deleterious to both sexes, they also must affect males more than females. A frequently overlooked problem is that relative strength of selection on males versus females may vary between environments, with social conditions being particularly likely to affect selection in males and females differently. Here, we induced mutations in red flour beetles (Tribolium castaneum) and tested their effect in both sexes under three different operational sex ratios (1:2, 1:1 and 2:1). Induced mutations decreased fitness of both males and females, but their effect was not stronger in males. Surprisingly, operational sex ratio did not affect selection against deleterious mutations nor its relative strength in the sexes. Thus, our results show no support for the role of sexual selection in the evolutionary maintenance of sex.     

The secondary sex ratio in Israel: 1980–1995

Abstract

This study deals with models and hypotheses that attempt to explain the underlying mechanisms determining the sex ratios at birth in human populations. Since the factors responsible are still questionable and research results are contradictory, we examine data available in Israel on the sex ratios at birth among two different sociodemographic groups, Jews and Moslems. Results suggest a difference between Jewish and Moslem patterns of secondary sex ratios with respect to parental age, education, and birth number. The difference may be described as a more regular and, by existing models, a more predictable pattern of secondary sex ratio among Moslems than among Jews. The possibility that Jewish religious laws play a role in this difference is discussed.     

Could maternal testosterone levels govern mammalian sex ratio deviations?

Although maternal dominance and good condition are frequently associated with raised offspring sex ratios in mammals, the key factor may be female testosterone, which not only underpins the behavioural indicators but could also provide a pathway to a possible proximate mechanism for sex determination. By taking into account the fact that female testosterone levels rise in response to environmental stressors, it is possible to re-interpret the findings of atypical sex ratios in mammals in a way that reconciles seemingly conflicting results and reveals instead what could be a coherent, adaptive system of sex allocation in mammals.     

The loss of Y-sperm in “sex ratio” (SR) males of Drosophila subobseura is compensated

In Drosophila subobscura sex ratio (SR) males, a mechanism compensating for the loss of Y-sperm is present since these males produced a higher number of female offspring than did males of three control strains. Moreover, the number of female offspring from SR-males was even higher (average 1719) than the number of female and male offspring together (average 1460) from T2, one of the control strains. The fertile life span of SR-males was found to lie between those of the control strains. The rate of insemination was the same for SR- and control males.     

Does the timing of attainment of maturity influence sexual size dimorphism and adult sex ratio in turtles?

The attainment of sexual maturity has been shown to affect measures of sexual size dimorphism (SSD) and adult sex ratios in several groups of vertebrates. Using data for turtles, we tested the model that sex ratios are expected to be male‐biased when females are larger than males and female‐biased when males are larger than females because of the relationship of each with the attainment of maturity. Our model is based on the premise that the earlier‐maturing sex remains smaller, on average throughout life, and predominates numerically unless the sexes are strongly affected by differential mortality, differential emigration, and immigration, or biased primary sex ratios. Based on data for 24 species in seven families, SSD and sex ratios were significantly negatively correlated for most analyses, even after the effect of phylogenetic bias was removed. The analyses provide support for the model that SSD and adult sex ratios are correlated in turtles as a result of simultaneous correlation of each with sexual differences in attainment of maturity (bimaturism). Environmental sex determination provides a possible mechanism for the phenomenon in turtles and some other organisms. © 2014 The Authors. Biological Journal of the Linnean Society published by John Wiley & Sons Ltd on behalf of The Linnean Society of London, Biological Journal of the Linnean Society, 2014, 112 , 142–149.     

Are brood sex ratios adaptive?—The effect of experimentally altered brood sex ratio on nestling growth,mortality and recruitment

Brood sex ratios (BSRs) have often been found to be nonrandom in respect of parental and environmental quality, and many hypotheses suggest that nonrandom sex ratios can be adaptive. To specifically test the adaptive value of biased BSRs, it is crucial to disentangle the consequences of BSR and maternal effects. In multiparous species, this requires cross-fostering experiments where foster parents rear offspring originating from multiple broods, and where the interactive effect of original and manipulated BSR on fitness components is tested. To our knowledge, our study on collared flycatchers (Ficedula albicollis) is the first that meets these requirements. In this species, where BSRs had previously been shown to be related to parental characteristics, we altered the original BSR of the parents shortly after hatching by cross-fostering nestlings among trios of broods and examined the effects on growth, mortality and recruitment of the nestlings. We found that original and experimental BSR, as well as the interaction of the two, were unrelated to the fitness components considered. Nestling growth was related only to background variables, namely brood size and hatching rank. Nestling mortality was related only to hatching asynchrony. Our results therefore do not support that the observed BSRs are adaptive in our study population. However, we cannot exclude the possibility of direct effects of experimentally altered BSRs on parental fitness, which should be evaluated in the future. In addition, studies similar to ours are required on various species to get a clearer picture of the adaptive value of nonrandom BSRs.     

Can overexpression of TGF—β1 gene change the sex ratio in transgenic mice？

Mouse TGF-β1 gene was microinjected into male pronuclei of F2 hybrid fertilized eggs obtained by mating CSJLF1 and C57BL/6J inbred strains to generate transgenic mice with over-expressed TGF-β1 gene.The rate of founder production is 31% and Southern blot analysis of founder mice tail DNAs gave an integration efficiency of 33%.TGF-β1 gene could be stably integrated to the chromosomes of transgenic mice and transmitted to their progeny at a rate of 33% in the second generation.Dot blot analysis of tail RNA of some transgenic mice indicated a moderate expression of the transgene.The most interestin finding of the present work is the striking eviation from the normal male:female sex ratio in transgenic mice,with an average ratio of 6.7:1.The possible nature of the predominance of male sex in transgenic mice overexpressing TGF-β1 is discussed.     

Against the odds? Nestling sex ratio variation in green-rumped parrotlets

We investigated nestling sex ratio variation in the green-rumpedparrotlet (Forpus passerinus), a small neotropical parrot breedingin central Venezuela. There are strong theoretical reasons topredict a female-biased sex ratio in this system according tothe local resource hypothesis; juvenile males are philopatricand there are high levels of competition between male siblingsfor access to breeding females. Data were collected from twobreeding sites over a 14-year period incorporating 564 broodswith a total of 2728 nestlings. The mean percentage of malenestlings across years was 51%. Despite extreme hatching asynchronyin this system and increased survival of earlier hatched offspring,there was no bias in sex allocation associated with egg sequence.Patterns in sex allocation were not associated with clutch size,age, or size of the breeding female or breeding site. The potentialfor selective resorption of eggs was considered; however, nosignificant relationship was found between extended laying intervalsand the sex of subsequent eggs. Together, these results suggestthat female parrotlets are unable to regulate the sex ratioof their clutch at laying or that facultative manipulation ofnestling sex ratio may not confer a fitness benefit to breedersin these populations.     

Is drift ‘directional’? Unequal breeding sex ratio revisited

Unequal breeding sex ratio can significantly reduce effective population size, allowing a rare neutral allele to jump to a high frequency through genetic drift. However, this one-way alteration to allele frequency appears inconsistent with the concept that drift is non-directional. Based on binomial sampling distribution, this study developed a method to directly and exhaustively measure drift by calculating the mean deviation of change in allele frequency, then applied it to cases of unequal breeding sex ratio. The result shows that, under those cases, (1) the mean deviation can always be divided into two halves that are equal in size but opposite in direction; (2) each half consists of one or several categories represented by various allele proportions in the rare sex; (3) this proportion is another factor that determines the outcome of drift, in addition to effective population size and allele frequency; (4) drift is non-directional on a global scale, but whether an allele will drift up or down can be predicted based on the above factors. This method enables us to dissect every component of the expected change in allele frequency caused by drift and to find out the combined effect of population size, allele frequency and allele proportion in the rarer sex under neutrality but unequal breeding sex ratio.     

Sex ratio variation and mixed pairs in roe deer: evidence for control of sex allocation?

Sex allocation has provided rich ground for the development of evolutionary theory. The dominant models in vertebrates have provided predictions of sex ratio based on asymmetry in variance in breeding success between sexes in the breeding system, and the relative effect of local competition. In ungulates, empirical work has provided some support for these models, but has also generated apparently contradictory observations. Recent models have provided some predictions for both individual and population sex ratio, showing that the availability of high-quality habitat patches and dispersal rates can critically affect both population- and individual-level expectations. We explore patterns in offspring sex ratio among a large sample of roe deer, a species with some interesting aspects of the breeding system. We found that in singleton pregnancies (the minority) there was an excess of male embryos, which was more marked in does in good condition at most sites. While the sex ratio among twins was close to parity, and unaffected either by average condition among populations or by individual condition within populations, we observed a clear excess of mixed pregnancies (sub-binomial variance, SBV). The excess was greater where the average condition was high. Within sites, population changes in average condition were associated with changes in SBV: in populations declining in condition, SBV also declined. There was no tendency for mixed twins to be more likely in individuals in better condition within a population. We conclude that condition-dependent allocation of sex does occur in roe deer. We suggest that in these "income breeders", mixed pairs might offer the greatest opportunity to optimize maternal investment during lactation, when conditions will be unpredictable, and that this is increasingly the case when average condition is poor.