Adjustment Of Offspring Sex Ratio Research Articles

Offspring sex ratio increases with paternal reproductive success in a colony of southern elephant seals

AbstractIn polygynous species, male reproductive success is often determined by their ability to dominate female harems. Harem‐holders sire a disproportionate number of offspring. Male dominance tends to correlate with age, but intense competition and early male mortality limit most males from achieving high social status. To maximize reproductive success despite low rank, offspring sex ratio adjustment may have evolved, favoring the sex with higher fitness. If traits influencing dominance are heritable and confer reproductive advantages, we expect fathers with higher reproductive success to produce more sons, as they are more likely to become dominant. In contrast, subordinate males with lower success may benefit from siring more daughters. We tested this hypothesis on a colony of southern elephant seals breeding on the Kerguelen Archipelago. We used genetic markers to link the paternity of 540 pups to 58 breeding males. We found that the probability of siring a son increases from 43% to 54% with paternal relative reproductive success, supporting the offspring sex ratio adjustment hypothesis. Given that various factors influence sex ratio in a population, future studies should tease apart these ecological processes (e.g., paternal dominance, maternal condition, local density, or adult sex ratio) and investigate how they interact with each other.

A possible case of offspring sex manipulation as result of a biased adult sex ratio

Although random meiosis should prevent the facultative adjustment of offspring sex ratio, theory predicts that females should produce more of the sex with the higher reproductive value. We reported a case of offspring sex ratio manipulation in grass wrens Cistothorus platensis. Males in better body condition would have higher reproductive value than females due to the potential for social polygyny and extra-pair fertilizations. On the other hand, local demography influences reproductive strategies in grass wrens as male abundance affects both social polygyny and extra-pair paternity frequencies. We evaluated whether females bias their brood sex ratio in response to adult sex ratio and nestling body condition (a proxy for female’s prospects of producing high-quality males). Females raised more male offspring when males were less abundant in the population (female-biased adult sex ratio). However, we found no relationship between nestling body condition and brood sex ratio, suggesting that females did not bias the brood sex ratio towards males when able to raise nestlings in better body condition. Taken together, our results provide the first suggestive evidence that female birds can manipulate their offspring sex ratio in response to the adult sex ratio.

Variance in offspring sex ratio and maternal allocation in a highly invasive mammal.

Skewed sex ratios at birth are widely reported in wild populations, however, the extent to which parents are able to modulate the sex ratio of offspring to maximize their own fitness remains unclear. This is particularly true for highly polytocous species as maximizing fitness may include trade-offs between sex ratio and the size and number of offspring in litters. In such cases, it may be adaptive for mothers to adjust both the number of offspring per litter and offspring sex to maximize individual fitness. Investigating maternal sex allocation in wild pigs (Sus scrofa) under stochastic environmental conditions, we predicted that under favorable conditions, high-quality mothers (larger and older) would produce male-biased litters and invest more in producing larger litters with more males. We also predicted sex ratio would vary relative to litter size, with a male-bias among smaller litters. We found evidence that increasing wild boar ancestry, maternal age and condition, and resource availability may weakly contribute to male-biased sex ratio, however, unknown factors not measured in this study are assumed to be more influential. High-quality mothers allocated more resources to litter production, but this relationship was driven by adjustment of litter size, not sex ratio. There was no relationship between sex ratio and litter size. Collectively, our results emphasized that adjustment of litter size appeared to be the primary reproductive characteristic manipulated in wild pigs to increase fitness rather than adjustment of offspring sex ratio.

Brood Sex Ratio in European Honey Buzzards Pernis apivorus is Related to Spring Phenology

In sexually size-dimorphic bird species, rearing costs of sons and daughters usually differ and may be important in the evolution of offspring sex ratio adjustment. Raptors have reversed sexual size dimorphism and the smaller males are sometimes found to be overrepresented in food-poor territories or years. As a raptor with small reversed sexual dimorphism (6% in body mass), the European Honey Buzzard Pernis apivorus is expected to show little or no brood sex ratio bias in relation to environmental conditions. We molecularly sexed 311 chicks of 195 broods in and around The Netherlands, during 1996–2014. We examined which environmental factors explained brood sex ratio variation best. Overall, sex ratio was not biased (all nests pooled: 50.8% females) but more females were produced in years when on average Honey Buzzards bred earlier (32% sex ratio change over a ten-day range in annual mean laying date). Within-year laying date variation, hatching order, abundance of wasp (Vespinae) nests (main food source) and summer weather did not explain sex ratio variation. In the Veluwe and Drenthe (1974–2014), Honey Buzzards laid eggs earlier when the spring was warmer, which resulted in a c. 9-day advance in laying date over 40 years. As warm spring weather was also a predictor of a higher density of wasp colonies, we expected female chicks to benefit more from growing up in wasp-rich years than males, if the sex ratio biases were adaptive. However, this differential growth benefit was not noticeable in chick body mass; chick body mass was best explained by negative effects of relative laying date (within a year) and hatching order. The potential benefit for female nestlings (compared to males) of growing up in years with warm springs, when egg laying occurs early and wasp colonies are more abundant, remains unknown.

Offspring sex ratio and partially asynchronous hatching in the Little Bittern (Ixobrychus minutus) population in south-western Slovakia

Birds are one of the best-studied animal groups in Europe. Despite this, there are several bird species, including the Little Bittern (Ixobrychus minutus), of which the breeding biology is still little known. Here, I examine the sex of offspring in relation to hatching order, the degree of hatching asynchrony and some other aspects of nesting biology (such as breeding phenology, clutch size, egg and nestling survival) of the Little Bittern in the south-western Slovakian population. Egg-laying occurred from 5 May to 10 July, but the majority of clutches were initiated in May. Mean clutch size was 5.2 ± 0.92 (SD) eggs. Parents initiated full incubation predominantly after laying the third egg (86.4% of cases) of the clutch, which led to only partially asynchronous hatching of eggs. However, no evidence was found for offspring sex ratio adjustment according to hatching order. Nevertheless, survival rates of eggs and nestlings were relatively high (80.9% and 94.3 %, respectively). The possible causes of observed patterns are discussed.

Males can adjust offspring sex ratio in an adaptive fashion through different mechanisms.

Sex allocation research has primarily focused on offspring sex-ratio adjustment by mothers. Yet, fathers also benefit from producing more of the sex with greater fitness returns. Here, we review the state-of-the art in the study of male-driven sex allocation and, counter to the current paradigm, we propose that males can adaptively influence offspring sex ratio through a wide variety of mechanisms. This includes differential production and motility of X- versus Y-bearing sperms in mammals, variation in seminal fluid composition in haplo-diploid invertebrates, and epigenetic mechanisms in some fish and lizards exhibiting environmental sex determination. Conflicts of interest between mothers and fathers over offspring sex ratios can emerge, although many more studies are needed in this area. While many studies of sex allocation have focused on adaptive explanations with little attention to mechanisms, and vice versa, the integration of these two topics is essential for understanding male-driven sex allocation.

Egg load is a cue for offspring sex ratio adjustment in a fig-pollinating wasp with male-eggs-first sex allocation.

Fig-pollinating wasps (Agaonidae) only reproduce within fig treeinflorescences (figs). Agaonid offspring sex ratios are usually female-biased and often concur with local mate competition theory (LMC). LMC predicts less female-bias when several foundresses reproduce in a fig due to reduced relatedness among intra-sexually competing male offspring. Clutch size, the offspring produced by each foundress, is a strong predictor of agaonid sex ratios and correlates negatively with foundress number. However, clutch size variation can result from several processes including egg load (eggs within a foundress), competition among foundresses and oviposition site limitation, each of which can be used as a sex allocation cue. We introduced into individual Ficus racemosa figs single Ceratosolen fusciceps foundresses and allowed each to oviposit from zero to five hours thus variably reducing their eggs-loads and then introduced each wasp individually into a second fig. Offspring sex ratio (proportion males) in second figs correlated negatively with clutch size, with males produced even in very small clutches. Ceratosolen fusciceps lay mainly male eggs first and then female eggs. Our results demonstrate that foundresses do not generally lay or attempt to lay a 'fixed' number of males, but do 'reset to zero' their sex allocation strategy on entering a second fig. With decreasing clutch size, gall failure increased, probably due to reduced pollen. We conclude that C.fusciceps foundresses can use their own egg loads as a cue to facultatively adjust their offspring sex ratios and that foundresses may also produce more 'insurance' males when they can predict increasing rates of offspring mortality.

Non-quantitative adjustment of offspring sex ratios in pollinating fig wasps.

Fig wasp is one of the most well known model systems in examining whether or not the parents could adjust their offspring sex ratio to maximize their gene frequency transmission in next generations. Our manipulative experiments showed that, in all of the five pollinator wasps of figs (Agaonidae) that have different averages of foundress numbers per syconium, almost the same proportions of male offspring are produced in the experiment that foundresses deposit one hour then are killed with ether (66.1%–70.1%) and over the lifespan of each foundress (14.0%–21.0%). The foundresses tend to deposit their male eggs prior to female eggs. The observed increase in the proportion of male offspring as a function of foundress number results from density-dependent interference competition among the foundresses. These results showed that the selection of gene frequency transmission through the behavioral adjustment in the evolution of sex ratio does not exist in these five fig wasps. The results here implied that genetic adjustment mechanisms of the sex ratio of fig wasps can only be triggered to be on or off and that the foundresses can not quantitatively adjust their sex ratio according to increased environmental selection pressure.

High density, maternal condition, and stress are associated with male-biased sex allocation in a marsupial

Many mammals have been reported to significantly bias their offspring sex ratios, but these deviations from equality have been difficult to understand and are often inconsistent even within the same species. Evolutionary theory predicts a number of scenarios where females should bias their investment to one sex over the other; when fitness returns are sex specific, selection favors the facultative adjustment of offspring sex ratios to the sex with the highest inclusive fitness return. Interpreting sex allocation in mammals within the framework of classic sex allocation theory is challenging given the complex life histories and social interactions of species, hence it is likely that there are multiple mechanisms and selective forces dependent upon maternal and environmental drivers. Here, we show the previously demonstrated condition-dependent sex allocation in bridled nailtail wallabies (Onychogalea fraenata), where females in better condition were more likely to have sons, was reversed under high population densities and elevated maternal stress. In this solitary species, an elevated glucocorticoid stress response under unnaturally high densities likely influences adaptive sex allocation to the dispersive sex, consistent with the local resource competition theory. Managing factors such as population density, maternal stress, and food resources may be used to adjust offspring sex ratios in this endangered species.

Maternal condition but not corticosterone is linked to offspring sex ratio in a passerine bird.

There is evidence of offspring sex ratio adjustment in a range of species, but the potential mechanisms remain largely unknown. Elevated maternal corticosterone (CORT) is associated with factors that can favour brood sex ratio adjustment, such as reduced maternal condition, food availability and partner attractiveness. Therefore, the steroid hormone has been suggested to play a key role in sex ratio manipulation. However, despite correlative and causal evidence CORT is linked to sex ratio manipulation in some avian species, the timing of adjustment varies between studies. Consequently, whether CORT is consistently involved in sex-ratio adjustment, and how the hormone acts as a mechanism for this adjustment remains unclear. Here we measured maternal baseline CORT and body condition in free-living blue tits (Cyanistes caeruleus) over three years and related these factors to brood sex ratio and nestling quality. In addition, a non-invasive technique was employed to experimentally elevate maternal CORT during egg laying, and its effects upon sex ratio and nestling quality were measured. We found that maternal CORT was not correlated with brood sex ratio, but mothers with elevated CORT fledged lighter offspring. Also, experimental elevation of maternal CORT did not influence brood sex ratio or nestling quality. In one year, mothers in superior body condition produced male biased broods, and maternal condition was positively correlated with both nestling mass and growth rate in all years. Unlike previous studies maternal condition was not correlated with maternal CORT. This study provides evidence that maternal condition is linked to brood sex ratio manipulation in blue tits. However, maternal baseline CORT may not be the mechanistic link between the maternal condition and sex ratio adjustment. Overall, this study serves to highlight the complexity of sex ratio adjustment in birds and the difficulties associated with identifying sex biasing mechanisms.

Genetics of decayed sexual traits in a parasitoid wasp with endosymbiont-induced asexuality.

Trait decay may occur when selective pressures shift, owing to changes in environment or life style, rendering formerly adaptive traits non-functional or even maladaptive. It remains largely unknown if such decay would stem from multiple mutations with small effects or rather involve few loci with major phenotypic effects. Here, we investigate the decay of female sexual traits, and the genetic causes thereof, in a transition from haplodiploid sexual reproduction to endosymbiont-induced asexual reproduction in the parasitoid wasp Asobara japonica. We take advantage of the fact that asexual females cured of their endosymbionts produce sons instead of daughters, and that these sons can be crossed with sexual females. By combining behavioral experiments with crosses designed to introgress alleles from the asexual into the sexual genome, we found that sexual attractiveness, mating, egg fertilization and plastic adjustment of offspring sex ratio (in response to variation in local mate competition) are decayed in asexual A. japonica females. Furthermore, introgression experiments revealed that the propensity for cured asexual females to produce only sons (because of decayed sexual attractiveness, mating behavior and/or egg fertilization) is likely caused by recessive genetic effects at a single locus. Recessive effects were also found to cause decay of plastic sex-ratio adjustment under variable levels of local mate competition. Our results suggest that few recessive mutations drive decay of female sexual traits, at least in asexual species deriving from haplodiploid sexual ancestors.

Does monogeny enable gall midges (Diptera: Cecidomyiidae) to regulate their sex ratio?

Monogeny, the production of unisexual broods by individual females, is widely recorded in gall midges (Diptera: Cecidomyiidae). Theoretical models propose that the adjustment of offspring sex ratio by females may pre-dispose the evolution of monogeny in gall midges however empirical studies in this field are superficial. Expressed more simply, monogeny may enable individual female gall midges to decrease or increase the number of male and female progeny they produce in response to changes in environmental conditions. Host quality/size is repeatedly reported to influence sexual investment in insects in terms of sex ratio adjustment. In this paper, we examined the sex ratio of the offspring of the monogenous predatory gall midge Aphidoletes aphidimyza attacking low and high abundances of the cotton aphid, Aphis gossypii. Two consecutive generations of female gall midges were presented with either a low or high abundance of aphids in each generation and the sex ratio of their progenies determined. There was no difference between the sex ratio of the progenies that developed on the high or low abundance of A. gossypii in the two generations. Apparently, the females did not regulate the number of female and male progenies, or adjust the numbers of male or female's eggs they produced in response to the changes in the abundance of prey. Results of this study do not support the theory of sex ratio regulation proposed for monogenous gall midges. It is likely that the skewed sex ratio in most species of monogenous gall midges is a consequence of differential mortality of male and female progenies under harsh conditions. The finding that male and female larvae did not differ in the number of aphids they require to complete their development supports this claim.

Progeny sex ratios in a short-lived lizard: seasonal invariance despite sex-specific effects of hatching date on fitness

When fitness returns are sex-specific, selection should favor the facultative adjustment of offspring sex ratios. Seasonal shifts in offspring sex ratios are predicted to be particularly beneficial in short-lived, sexually dimorphic species in which hatching date is linked to adult size, which is related to fitness in a sex-specific fashion. We used four time series of hatching dates and progeny sex ratios in the brown anole (Anolis sagrei), a short-lived lizard with male-biased sexual size dimorphism, to test for such a seasonal shift in progeny sex ratio. In 2 of the 4 years, we also released hatchlings to their natural environment to test for sex-specific effects of hatching date on juvenile survival and adult size. We found that the relationship between hatching date and size the following year was significantly steeper in males than in females, and previous work has shown that adult size is more strongly tied to fitness in males than in females. Based on those results and on further evidence linking hatching date and body size to sex-specific survival and reproductive success, we predicted that sex ratios should shift from male- to female-biased as the breeding season progressed. Contrary to our prediction, we detected no clear seasonal shift in progeny sex ratio. Furthermore, although juvenile survival was correlated with hatching date, this relationship did not consistently differ between the sexes. The observation that progeny sex ratios are seasonally invariant despite several apparent links to adult fitness suggests that the evolution of a seasonal sex-ratio bias is either inherently constrained or requires a stronger selective advantage with respect to juvenile survival.

Mixed sex allocation strategies in a polytocous mammal, the house mouse (Mus musculus)

The issue of adaptive adjustment of offspring sex ratio (proportion of male births) in polytocous mammals, producing several offspring per litter, is controversial because females of these species can maximize their fitness mainly by adjusting offspring number. To address this issue, we examined the effect of maternal condition at mating, experimentally decreased by pre-mating food restriction, on the sex ratio variation in 137 female mice. We tested two basic sex allocation hypotheses plausible for polytocous mammals: (1) the Myers hypothesis, predicting that cheaper sex should be favored in poor environmental conditions to maximize offspring number; and (2) the Williams hypothesis, predicting maximum fitness returns by adjusting size- and sex-specific composition of the litter according to the maternal condition. The food-restricted mothers produced larger litters with a higher proportion of cheaper daughters than the control mothers. By contrast, the control mothers optimized size and sex composition of the litter according to their weight at mating. In addition, the offspring of the food-restricted mothers suffered less from pre-weaning mortality than those of the control mothers. Therefore, when comparing the groups, the Myers hypothesis had a general significance while the Williams hypothesis was plausible only for the control mothers. Furthermore, some of the food-restricted mothers partly coped with the pre-mating food restriction and increased the proportion of sons in the litter with the increasing maternal weight loss (during the period of food restriction). The sex ratio variation was thus a result of three sex allocation strategies depending on the maternal condition at mating.

Maternal stress to partner quality is linked to adaptive offspring sex ratio adjustment

Female birds have been shown to have a remarkable degree of control over the sex ratio of the offspring they produce. However, it remains poorly understood how these skews are achieved. Female condition, and consequent variation in circulating hormones, provides a plausible mechanistic link between offspring sex biases and the environmental and social stresses commonly invoked to explain adaptive sex allocation, such as diet, territory quality, and body condition. However, although experimental studies have shown that female perception of male phenotype alone can lead to sex ratio biases, it is unknown how partner quality influences female physiological state. Using a controlled within-female experimental design where female Gouldian finches (Erythrura gouldiae) bred with both high- and low-quality males, we found that partner quality directly affects female hormonal status and subsequent fitness. When constrained to breeding with low-quality males, females had highly elevated stress responses (corticosterone levels) and produced adaptive male-biased sex ratios, whereas when they bred with high-quality males, females had low corticosterone levels and produced an equal offspring sex ratio. There was no effect of other maternal hormones (e.g., testosterone) or body condition on offspring sex ratios. Female physiological condition during egg production, and variation in circulating hormones in particular, may provide a general mechanistic route for strategic sex allocation in birds.

No evidence for offspring sex-ratio adjustment to social or environmental conditions in cooperatively breeding purple-crowned fairy-wrens

When fitness returns or production costs vary between male and female offspring, selection is expected to favor females that adjust offspring sex ratio accordingly. However, to what extent vertebrates can do so is the subject of ongoing debate. Here, we explore primary sex ratios in 125 broods of cooperatively breeding purple-crowned fairy-wrens Malurus coronatus. We expected that females might adjust offspring sex ratio because this passerine species experiences considerable variation in social and environmental conditions. (1) However, although helpers substantially increase parental fitness, females (particularly in pairs and small groups) did not overproduce philopatric males (helper-repayment hypothesis). (2) Sex-ratio adjustment based on competition among individuals (helper-competition hypothesis) did not conceal helper-repayment effects or drive sex allocation on its own: while high-quality territories can accommodate more birds, brood sex ratios were independent of territory quality, alone or in interaction with group size. (3) Additionally, males are larger than females and are possibly more costly to produce (costly sex hypothesis), and (4) female offspring may benefit more from long-term effects of favorable conditions early in life (Trivers–Willard hypothesis). Nonetheless, large seasonal variation in food abundance was not associated with a consistent skew in primary sex ratios. Thus, overall, our results did not support the main hypotheses of adaptive sex-ratio adjustment in M. coronatus. We discuss that long-term differential costs and benefits may be insufficient to drive evolution of primary sex-ratio manipulation by M. coronatus females. More investigation is therefore needed to determine the general required sex differences in long-term fitness returns for mechanisms of primary sex-ratio manipulation to evolve.

Change in Body Mass Can Overrule the Effects of Maternal Testosterone on Primary Offspring Sex Ratio of First Eggs in Homing Pigeons

The phenomenon of primary offspring sex ratio adjustment is being extensively studied, yet knowledge of the underlying proximate mechanism is still mainly hypothetical. Female birds are the heterogametic sex, thus potentially controlling the sex of the gamete to be fertilized. In several bird species, independent studies showed effects of maternal plasma testosterone, corticosterone, or condition on primary offspring sex ratio. Our objective was to investigate the causal relation between these two maternal hormones, body condition, and offspring sex ratio in homing pigeons (Columba livia domestica). Following our earlier study, we again implanted females with testosterone and determined embryo sex of first eggs. To identify the pathway of sex ratio adjustment, we repeatedly measured not only maternal plasma testosterone and mass but also plasma corticosterone, cholesterol, and glucose, all indicators of body condition. We also calculated the temporal change in these parameters, which has been proposed to be a more accurate predictor of offspring sex ratio compared with the absolute values. Furthermore, we analyzed testosterone concentrations in outer yolk layers, which potentially influence the first meiotic division of the gamete. We found no relation between plasma parameter and embryo sex of first eggs; testosterone treatment did not affect any of the measured parameters. However, females that increased in mass produced more male embryos, irrespective of treatment group. Outer yolk layer testosterone concentrations did not differ between treatment groups or between male and female eggs. We propose that not only the absolute values but also the complex interactions between maternal hormones and body condition ultimately affect the mechanism of primary offspring sex manipulation.

Nestling sex ratio of golden‐winged warblers Vermivora chrysoptera in an introgressed population

Sex ratio biases in avian species remain controversial, although several studies have documented apparent facultative adjustment of offspring sex ratios. While hybridizing pied and collared flycatchers have exhibited sex ratio skews that may be a response to sex‐based costs associated with hybridization, this appears not to be true of a hybridized population of blue‐winged Vermivora pinus and golden‐winged V. chrysoptera warblers. We examined the primary sex ratio of nestlings in a population of hybrid and introgressed golden‐winged warblers. The sex ratio of 298 nestlings from 81 nests in the population was approximately 50:50. We conducted paternity assignments and analyzed groups of nestlings with shared genetic parents (“genetic broods”) and found no difference from the expected binomial distribution, and no statistically significant relationship between parental species phenotype and nestling sex ratio. We saw no evidence of preferential production of male or female nestlings, and female hybrids were found to mate and breed in the population. This suggests that heterogametic (female) hybrids are both viable and fertile, and thus that Haldane's Rule does not apply to this system. While populations of hybridizing golden‐winged warblers should be monitored for evidence of costs of heterospecific pairings, it is unlikely that adjustment of sex ratios would be the form of compensation for sub‐optimal mating conditions. Our results provide support for the emerging hypothesis that hybrids suffer no disadvantage relative to golden‐winged and blue‐winged warblers.

Offspring sex ratio in the sequentially polygamous Penduline Tit Remiz pendulinus

Despite the growing literature on facultative sex-ratio adjustment in chromosomal sex-determining vertebrate taxa (birds, mammals), the consistency of results is often low between studies and species. Here, we investigate the primary and secondary offspring sex ratio of a small passerine bird, the Eurasian Penduline Tit (Remiz pendulinus) in three consecutive years. This species has a uniquely diverse breeding system, in which the male (and/or the female) abandons the nest during egg-laying, and starts a new breeding attempt. This allowed us to test (1) whether patterns of parental care, i.e., male-only care, female-only care or biparental desertion, influence offspring sex ratio, and (2) whether the offspring sex ratio is repeatable between successive clutches of males and females. Using molecular markers to sex 497 offspring in 176 broods, we show that (1) offspring sex ratio does not depend on which parent provides care, and (2) the offspring sex ratio is not repeatable between clutches of a given individual. The overall primary and secondary offspring sex ratio at a population level is not different from parity (54 ± 6% males, and 50 ± 3% (mean ± SE), respectively). We suggest that ecological and phenotypic factors, rather than individual traits of parents, may influence offspring’s sex, and conclude that there is currently no evidence for a facultative adjustment of offspring sex ratio in the Penduline Tit.

Review. Meiotic drive and sex determination: molecular and cytological mechanisms of sex ratio adjustment in birds.

Differences in relative fitness of male and female offspring across ecological and social environments should favour the evolution of sex-determining mechanisms that enable adjustment of brood sex ratio to the context of breeding. Despite the expectation that genetic sex determination should not produce consistent bias in primary sex ratios, extensive and adaptive modifications of offspring sex ratio in relation to social and physiological conditions during reproduction are often documented. Such discordance emphasizes the need for empirical investigation of the proximate mechanisms for modifying primary sex ratios, and suggests epigenetic effects on sex-determining mechanisms as the most likely candidates. Birds, in particular, are thought to have an unusually direct opportunity to modify offspring sex ratio because avian females are heterogametic and because the sex-determining division in avian meiosis occurs prior to ovulation and fertilization. However, despite evidence of strong epigenetic effects on sex determination in pre-ovulatory avian oocytes, the mechanisms behind such effects remain elusive. Our review of molecular and cytological mechanisms of avian meiosis uncovers a multitude of potential targets for selection on biased segregation of sex chromosomes, which may reflect the diversity of mechanisms and levels on which such selection operates in birds. Our findings indicate that pronounced differences between sex chromosomes in size, shape, size of protein bodies, alignment at the meiotic plate, microtubule attachment and epigenetic markings should commonly produce biased segregation of sex chromosomes as the default state, with secondary evolution of compensatory mechanisms necessary to maintain unbiased meiosis. We suggest that it is the epigenetic effects that modify such compensatory mechanisms that enable context-dependent and precise adjustment of primary sex ratio in birds. Furthermore, we highlight the features of avian meiosis that can be influenced by maternal hormones in response to environmental stimuli and may account for the precise and adaptive patterns of offspring sex ratio adjustment observed in some species.