Sexual conflict in action: An antagonistic relationship between maternal and paternal sex allocation in the tammar wallaby,Notamacropus eugenii

Sex ratio biases are often inconsistent, both among and within species and populations. While some of these inconsistencies may be due to experimental design, much of the variation remains inexplicable. Recent research suggests that an exclusive focus on mothers may account for some of the inconsistency, with an increasing number of studies showing variation in sperm sex ratios and seminal fluids. Using fluorescent in‐situ hybridization, we show a significant population‐level Y‐chromosome bias in the spermatozoa of wild tammar wallabies, but with significant intraindividual variation between males. We also show a population‐level birth sex ratio trend in the same direction toward male offspring, but a weaning sex ratio that is significantly female‐biased, indicating that males are disproportionately lost during lactation. We hypothesize that sexual conflict between parents may cause mothers to adjust offspring sex ratios after birth, through abandonment of male pouch young and reactivation of diapaused embryos. Further research is required in a captive, controlled setting to understand what is driving and mechanistically controlling sperm sex ratio and offspring sex ratio biases and to understand the sexually antagonistic relationship between mothers and fathers over offspring sex. These results extend beyond sex allocation, as they question studies of population processes that assume equal input of sex chromosomes from fathers, and will also assist with future reproduction studies for management and conservation of marsupials.     

Cross‐fostering eggs reveals that female collared flycatchers adjust clutch sex ratios according to parental ability to invest in offspring

Across animal taxa, reproductive success is generally more variable and more strongly dependent upon body condition for males than for females; in such cases, parents able to produce offspring in above‐average condition are predicted to produce sons, whereas parents unable to produce offspring in good condition should produce daughters. We tested this hypothesis in the collared flycatcher (Ficedula albicollis) by cross‐fostering eggs among nests and using the condition of foster young that parents raised to fledging as a functional measure of their ability to produce fit offspring. As predicted, females raising heavier‐than‐average foster fledglings with their social mate initially produced male‐biased primary sex ratios, whereas those raising lighter‐than‐average foster fledglings produced female‐biased primary sex ratios. Females also produced male‐biased clutches when mated to males with large secondary sexual characters (wing patches), and tended to produce male‐biased clutches earlier within breeding seasons relative to females breeding later. However, females did not adjust the sex of individuals within their clutches; sex was distributed randomly with respect to egg size, laying order and paternity. Future research investigating the proximate mechanisms linking ecological contexts and the quality of offspring parents are able to produce with primary sex‐ratio variation could provide fundamental insight into the evolution of context‐dependent sex‐ratio adjustment.     

Sex ratio regulation in the waspEupelmus vuilleti (crwf.), an ectoparasitoid on bean weevil larvae (Hymenoptera: Pteromalidae)

In Africa, the seeds and/or pods ofVigna unguiculata andVigna radiata (Papilionacea) are attacked in fields and storage structures by bruchid beetlesCallosobruchus maculatus andBruchidius atrolineatus, on which parasitoid communities can develop. One of these parasitoids is the solitary ectoparasitoidEupelmus vuilleti (Eupelmidae). The storage conditions ofV. unguiculata andV. radiata favor the overlapping of all host stages during several months. These conditions suggest that female parasitoids would vary the sex ratio of their offspring according to the different sizes or developmental stages of hosts. The sex ratio ofE. vuilleti was strongly related to the developmental stage of the hostC. maculatus. Under our experimental conditions, where superparasitism is rare, the proportion of daughters varied between 5 and 25% on the third larval stage but reached 70 to 90% on the pupae. The increase in the proportion of daughters was also observed in the absence of superparasitism. In this case, there was an absolute coincidence between the sex ratio of eggs laid and that of emerged adults. Manipulation of the sex of the egg by the females seems to take place at the time of the egg's fertilization. The relation between host weight and egg sex showed that the male eggs are preferentially laid on lighter host larvae and the female eggs on heavier ones.     

Sexual dimorphism of egg size in the European Blackbird Turdus merula

Recently, a number of studies have shown that female birds are able to control the sex of their progeny at the stage of the gamete. There is also some evidence that females adjust their investment in offspring depending on the sex of the embryo during egg formation. Differential maternal investment to the eggs depending on their sex is usually interpreted as an adaptive strategy, by which females can increase competitive abilities of the smaller sex, or preferentially invest towards the sex with the potentially higher fitness returns. Here, we studied variation in egg size in relation to embryo sex and laying order in the European Blackbird Turdus merula. We found male and female eggs to differ in size, with larger eggs containing male embryos, as well as a significant interaction between embryo sex and laying order. This interaction resulted from the fact that egg size increased with the laying sequence among eggs bearing females but did not change with laying order among eggs bearing males. There was no relationship between offspring sex and the laying sequence within a clutch. We suggest that sexual dimorphism in egg size recorded in the European Blackbird may reflect favouritism of the sex which may give higher fitness returns.     

Offspring sex ratios in tree swallows: females in better condition produce more sons

Organisms are expected to adjust the sex ratio of their offspring in relation to the relative fitness benefits of sons and daughters. We used a molecular sexing technique that amplifies an intron of the CHD1 gene in birds to examine the sex ratio at egg-laying in socially monogamous tree swallows (Tachycineta bicolor). We examined all individuals in 40 broods (210 young), including all unhatched eggs and nestlings. Thus, the sex ratio we measured was the same as the sex ratio at laying. Overall, the mean sex ratio per brood (+/- SD) was biased significantly towards males (57 +/- 2% male). Within broods, male-biased sex ratios were associated with females in better body condition, and these females were more likely to produce sons in better condition. Tree swallows have one of the highest known levels of extra-pair paternity in birds (38-76% extra-pair young), and, as a consequence, variance in male reproductive success is greater than that of females. Thus, in tree swallows, investment in sons has the potential for higher fitness returns than investment in daughters, assuming that sons in better condition have greater reproductive success.     

Population consequences of maternal effects: sex‐bias in egg‐laying order facilitates divergence in sexual dimorphism between bird populations

Abstract When costs and benefits of raising sons and daughters differ between environments, parents may be selected to modify their investment into male and female offspring. In two recently colonized environments, breeding female house finches (Carpodacus mexicanus) modified the sex and growth of their offspring in relation to the order in which eggs were laid in a clutch. Here we show that, in both populations, these maternal effects strongly biased frequency distribution of tarsus size of fully grown males and females and ultimately produced population divergence in this trait. Although in each population, male and female offspring show a wide range of growth patterns, maternal modifications of sex‐ratio in relation to egg‐laying order resulted in under‐representation of the morphologies that were selected against and over‐representation of morphologies that were favoured by the local selection on juveniles. The result of these maternal adjustments was fast phenotypic change in sexual size dimorphism within and between populations. Maternal manipulations of offspring morphologies may be especially important at the initial stages of population establishment in the novel environments and may have facilitated recent colonization of much of North America by the house finch.     

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 tree inflorescences (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.     

Developmental stage of failed eggs in the red-legged partridge <Emphasis Type="Italic">Alectoris rufa</Emphasis>

Understanding whether egg failure occurs more frequently during laying or during incubation is important for determining the most vulnerable period of the egg phase in bird species with long laying and incubation periods. However, most studies compare nest failure during the egg stage and the hatchling stage. In this study we examined whether egg failure was higher during the laying period and early development than during the final stages of development in a population of red-legged partridge (Alectoris rufa) from northeast Spain. We collected 216 abandoned eggs in the field. Only 12% (n = 26) of the eggs were sufficiently intact to enable direct assessment of developmental stage, showing that 81% of 26 eggs were lost during early stages. The majority of eggs were depredated (n = 154, 71%), as evidenced by an opening hole. To take advantage of information contained in these eggs, we propose a simple method to assess their developmental stage by measuring the size of the opening of their hole. Based on this method, we estimated that the proportion of eggs lost during early stages ranged from 72 to 83%. We validated this result of a high percentage of egg failure during early developmental stages with a larger experimental sample. Nest losses in the partridge are higher during the laying period or early development. This result is important in that the direction of conservation efforts and their seasonal application should be adjusted to account for the most important factors affecting egg failure.     

Impaired hatching success and male-biased embryo mortality in Tree Sparrows

During the past 30 years, many species of farmland birds have declined dramatically in numbers in Northern Europe, a trend coinciding with a tremendous intensification of agriculture, although the exact causes of these declines remain unclear. One of the worst affected species is the Tree Sparrow (Passer montanus). We studied two Swedish Tree Sparrow populations during the years 1996–2004 and found that in both populations, almost half of all laid eggs remained unhatched. This led us to investigate whether the eggs failed to hatch because of: (1) eggs not being fertilised or (2) embryo mortality. Our analyses showed that all of the eggs investigated contained sufficient number of sperm for fertilisation and that they also had other visible signs indicating that fertilisation had occurred. Hatching failure was instead shown to result from embryo mortality. Using molecular techniques, we were able to determine that embryo mortality is more likely to affect male embryos than females and that the fledgling sex ratio was consequently highly female biased. The cause of this sex-biased embryo mortality remains unknown, but various potential explanations are discussed.     

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.     

Sex allocation and sex‐specific parental investment in an endangered seabird

Biased offspring sex ratio is relatively rare in birds and sex allocation can vary with environmental conditions, with the larger and more costly sex, which can be either the male or female depending on species, favoured during high food availability. Sex‐specific parental investment may lead to biased mortality and, coupled with unequal production of one sex, may result in biased adult sex ratio, with potential grave consequences on population stability. The African Penguin Spheniscus demersus, endemic to southern Africa, is an endangered monogamous seabird with bi‐parental care. Female adult African Penguins are smaller, have a higher foraging effort when breeding and higher mortality compared with adult males. In 2015, a year in which environmental conditions were favourable for breeding, African Penguin chick production on Bird Island, Algoa Bay, South Africa, was skewed towards males (1.5 males to 1 female). Males also had higher growth rates and fledging mass than females, with potentially higher post‐fledging survival. Female, but not male, parents had higher foraging effort and lower body condition with increasing number of male chicks in their brood, thereby revealing flexibility in their parental strategy, but also the costs of their investment in their current brood. The combination of male‐biased chick production and higher female mortality, possibly at the juvenile stage as a result of lower parental investment in female chicks, and/or at the adult stage as a result of higher parental investment, may contribute to a biased adult sex ratio (ASR) in this species. While further research during years of contrasting food availability is needed to confirm this trend, populations with male‐skewed ASRs have higher extinction risks and conservation strategies aiming to benefit female African Penguin might need to be developed.     

Sex and stochasticity affect range expansion of experimental invasions

Understanding and predicting range expansion are key objectives in many basic and applied contexts. Among dioecious organisms, there is strong evidence for sex differences in dispersal, which could alter the sex ratio at the expansion's leading edge. However, demographic stochasticity could also affect leading‐edge sex ratios, perhaps overwhelming sex‐biased dispersal. We used insects in laboratory mesocosms to test the effects of sex‐biased dispersal on range expansion, and a simulation model to explore interactive effects of sex‐biased dispersal and demographic stochasticity. Sex‐biased dispersal created spatial clines in the sex ratio, which influenced offspring production at the front and altered invasion velocity. Increasing female dispersal relative to males accelerated spread, despite the prediction that demographic stochasticity would weaken a signal of sex‐biased dispersal. Our results provide the first experimental evidence for an influence of sex‐biased dispersal on invasion velocity, highlighting the value of accounting for sex structure in studies of range expansion.     

Reproductive ecology of the jacky dragon (Amphibolurus muricatus): an agamid lizard with temperature‐dependent sex determination

Abstract The jacky dragon, Amphibolurus muricatus (White, ex Shaw 1790) is a medium sized agamid lizard from the southeast of Australia. Laboratory incubation trials show that this species possesses temperature‐dependent sex determination. Both high and low incubation temperatures produced all female offspring, while varying proportions of males hatched at intermediate temperatures. Females may lay several clutches containing from three to nine eggs during the spring and summer. We report the first field nest temperature recordings for a squamate reptile with temperature‐dependent sex determination. Hatchling sex is determined by nest temperatures that are due to the combination of daily and seasonal weather conditions, together with maternal nest site selection. Over the prolonged egg‐laying season, mean nest temperatures steadily increase. This suggests that hatchling sex is best predicted by the date of egg laying, and that sex ratios from field nests will vary over the course of the breeding season. Lizards hatching from eggs laid in the spring (October) experience a longer growing season and should reach a larger body size by the beginning of their first reproductive season, compared to lizards from eggs laid in late summer (February). Adult male A. muricatus attain a greater maximum body size and have relatively larger heads than females, possibly as a consequence of sexual selection due to male‐male competition for territories and mates. If reproductive success in males increases with larger body size, then early hatching males may obtain a greater fitness benefit as adults, compared to males that hatch in late summer. We hypothesize that early season nests should produce male‐biased sex ratios, and that this provides an adaptive explanation for temperature‐dependent sex determination in A. muricatus.     

Sex allocation conflict between queens and workers in Formica pratensis wood ants predicts seasonal sex ratio variation

Sex allocation theory predicts parents should adjust their investment in male and female offspring in a way that increases parental fitness. This has been shown in several species and selective contexts. Yet, seasonal sex ratio variation within species and its underlying causes are poorly understood. Here, we study sex allocation variation in the wood ant Formica pratensis. This species displays conflict over colony sex ratio as workers and queens prefer different investment in male and female offspring, owing to haplodiploidy and relatedness asymmetries. It is unique among Formica ants because it produces two separate sexual offspring cohorts per season. We predict sex ratios to be closer to queen optimum in the early cohort but more female‐biased and closer to worker optimum in the later one. This is because the power of workers to manipulate colony sex ratio varies seasonally with the availability of diploid eggs. Consistently, more female‐biased sex ratios in the later offspring cohort over a three‐year sampling period from 93 colonies clearly support our prediction. The resulting seasonal alternation of sex ratios between queen and worker optima is a novel demonstration how understanding constraints of sex ratio adjustment increases our ability to predict sex ratio variation.     

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.     

Sex ratio comparisons between nestlings and dead embryos of the Sparrowhawk Accipiter nisus

Sex ratios that differ from unity have been reported for several bird species, but are poorly understood. Skewed sex ratios may originate at ovulation (primary sex ratio) or arise through differential mortality between the sexes (secondary sex ratio). To estimate the primary sex ratio from nestlings is difficult because in some nests not all the offspring can be sexed. Both when including and excluding such nests, there is a risk of overestimating the proportion of the better-surviving sex. Here we sexed dead Sparrowhawk embryos to determine whether unhatched eggs affect primary sex ratio estimates that are based on nestling data. In nests in which embryo mortality occurred, there was up to a 9% discrepancy in the primary sex ratio estimates based on nestlings alone compared to nestlings and dead embryos together. There was no evidence that these differences were based on sex-specific causes of mortality of embryos.     

Internest sex-ratio variation and male brood survival in the ant Pheidole pallidula

Sex allocation in social insects has become a general modelin tests of inclusive fitness theory, sex-ratio theory, andparent-offspring conflict. Several studies have shown that colonysex ratios are often bimodally distributed, with some coloniesproducing mainly females and others mainly males. Sex specializationmay result from workers assessing their relatedness to malebrood versus female brood, relative to the average worker-relatednessasymmetry in other colonies of their population. Workers thenadjust the sex ratio in their own interest This hypothesis assumesthat workers can recognize the sex of the brood in their colonyand selectively eliminate males. We compared the primary sexratio (at the egg stage) and secondary sex ratio (reproductivepupae and adults) of colonies in the ant Pheidole pallidula.There was a strong bimodal distribution of secondary sex ratios,with most colonies producing mainly reproductives of one sex.In contrast, there was no evidence of a bimodal distributionof primary sex ratios. The proportion of haploid eggs producedby queens was 0.35 in early spring and decreased to about 0.1in summer. Male eggs also were present in virtually all fieldcolonies sampled in July, although eggs laid at this time ofyear never give rise to males. All male brood is, therefore,selectively eliminated beginning in July and continue to beeliminated through the rest of the year. Finally, the populationsex-ratio investment was female-biased. Together, these resultsare consistent with the hypothesis that workers control thesecondary sex ratio by selectively eliminating male brood inabout half the colonies, perhaps those with high relatednessasymmetry.[Behav Ecol 7: 292–298 (1996)]     

Temperature-dependent sex-biased embryo mortality in a bird

Sex ratios have important evolutionary consequences and are often biased by environmental factors. The effect of developmental temperature on offspring sex ratios has been widely documented across a diverse range of taxa but has rarely been investigated in birds and mammals. However, recent field observations and artificial incubation experiments have demonstrated that the hatching sex ratio of a megapode, the Australian brush-turkey (Alectura lathami), varied with incubation temperature; more females hatched at high incubation temperatures and more males hatched at low temperatures. Here, we investigated the causes of this temperature-dependent sex-biasing system. Molecular sexing of chicks and embryos confirmed that male embryo mortality was greater at high temperatures while female embryo mortality is greater at low temperatures, with mortality in both sexes similar at intermediate incubation temperatures. Temperature-dependent sex-biased embryo mortality represents a novel mechanism of altering sex ratios in birds. This novel mechanism, coupled with the unique breeding biology of the brush-turkey, offers a potentially unparalleled opportunity in which to investigate sex allocation theory in birds.     

Birth sex ratio in captive mammals: Patterns,biases, and the implications for management and conservation

Sex allocation theory predicts that a female should produce the offspring of the sex that most increases her own fitness. For polygynous species, this means that females in superior condition should bias offspring production toward the sex with greater variation in lifetime reproductive success, which is typically males. Captive mammal populations are generally kept in good nutritional condition with low levels of stress, and thus populations of polygynous species might be expected to have birth sex ratios biased toward males. Sex allocation theory also predicts that when competition reduces reproductive success of the mother, she should bias offspring toward whichever sex disperses. These predicted biases would have a large impact on captive breeding programs because unbalanced sex ratios may compromise use of limited space in zoos. We examined 66 species of mammals from three taxonomic orders (primates, ungulates, and carnivores) maintained in North American zoos for evidence of birth sex ratio bias. Contrary to our expectations, we found no evidence of bias toward male births in polygynous populations. We did find evidence that birth sex ratios of primates are male biased and that, within primates, offspring sex was biased toward the naturally dispersing sex. We also found that most species experienced long contiguous periods of at least 7 years with either male‐ or female‐biased sex ratios, owing in part to patterns of dispersal (for primates) and/or to stochastic causes. Population managers must be ready to compensate for significant biases in birth sex ratio based on dispersal and stochasticity. Zoo Biol 19:11–25, 2000. © 2000 Wiley‐Liss, Inc.     

Sex-specific effects of maternal immunization on yolk antibody transfer and offspring performance in zebra finches

Trans-generational antibody transfer constitutes an important mechanism by which mothers may enhance offspring resistance to pathogens. Thus, differential antibody deposition may potentially allow a female to differentiate offspring performance. Here, we examined whether maternal immunization with sheep red blood cells (SRBC) prior to egg laying affects sex-specific yolk antibody transfer and sex-specific offspring performance in zebra finches (Taeniopygia guttata). We showed that immunized mothers deposit anti-SRBC antibodies into the eggs depending on embryo sex and laying order, and that maternal exposure to SRBC positively affects the body size of female, but not male offspring. This is the first study reporting sex-specific consequences of maternal immunization on offspring performance, and suggests that antibody transfer may constitute an adaptive mechanism of maternal favouritism.