Manipulation of offspring sex ratio by second-mated female house wrens

In 1973, Trivers and Willard proposed that offspring sex ratio should be associated with the quality of parental care likely to be provided to the offspring. We tested this hypothesis by comparing fledgling sex ratios in nests of first- and second-mated female house wrens (Troglodytes aedon). In our Wyoming population, second-mated females typically receive little or no male parental assistance and fledge fewer and lower-quality young compared with first-mated females. Assuming that being of lower quality has stronger negative effects on the future reproductive success of males than that of females in this polygynous population, we predicted that fledgling sex ratios in the nests of second-mated females would be female-biased compared with the fledgling sex ratios of first-mated females. Additionally, we asked whether any sex bias at fledging could have resulted from male-biased nestling mortality caused by sex-biased parental provisioning. As predicted, mean fledgling sex ratios in nests of second-mated females were more female-biased than fledgling sex ratios in nests of first-mated females. However, we found no evidence of either sex-biased nestling mortality or sex-biased parental provisioning. These findings suggest that females are responding to their status as second-mated females and to the associated low-quality parental care that their young are likely to receive by producing female-biased clutches rather than manipulating the offspring sex ratio through sex-biased nestling mortality.     

Surplus nest boxes and the potential for polygyny affect clutch size and offspring sex ratio in house wrens

Females of many species can gain benefits from being choosy about their mates and even exhibit context-dependent investment in reproduction in response to the quality of their breeding situation. Here, we show that if a male house wren is provided with surplus nest boxes in his territory, his mate lays a larger clutch with a significantly higher proportion of sons. This response to a territory characteristic directly associated with male competitive ability, and ultimately to male reproductive success, suggests that male competition over access to high-quality territories with surplus nest boxes (i.e. those able to support polygyny) may influence female reproductive investment decisions. The results of this study have interesting implications, particularly considering the important role that studies of cavity nesting birds utilizing nest boxes have played in advancing our understanding of behaviour, ecology and evolution.     

Egg size, offspring sex and hatching asynchrony in zebra finches Taeniopygia guttata

Experimental synchronization of onset of incubation was employed in laboratory held zebra finches Taeniopygia guttata to study whether differential resource allocation and possible bias of offspring sex in subsequent eggs in the laying order could mitigate the effects of hatching asynchrony. We found that egg mass increased with laying order, but offspring sex was not related to laying order. Among synchronized clutches, eggs hatched more synchronously than eggs from control nests. Survival probability was related to egg mass, and as expected, this effect differed between experimental groups: it was positive among synchronized broods and not significantly related among asynchronous broods. This suggests that increase in egg mass with the laying order might reduce disparities between early and late hatching chicks. Female nestlings survived better than male nestlings. However their growth was impaired in synchronized broods, whilst growth of males was not affected by hatching synchronization.     

Social mating system and reproductive success in house wrens

Current models explaining the establishment and maintenanceof social monogamy and polygyny within avian populations typicallyassume that the reproductive success of polygynous males exceedsthat of monogamous males. This assumption is almost always supportedwhen the number of fledglings or recruits to future breedingpopulations is used to measure adult reproductive success. However,recent studies using DNA markers indicate that simple countsof fledglings or recruits may be a poor estimator of the numberof nestlings sired by the social father. In this paper, we comparethe number of genetic offspring produced by socially monogamousand polygynous house wren (TrogiodyUs atdon) males in nestsat which they were the social father. Polygynous males did,in fact, sire more nestlings in their own nests than did monogamousmales. Moreover, although we have not identified the sires ofextrapair nestlings, we document that even when all extrapairnestlings in this population are hypotheticaOy assigned to monogamousmales, die total reproductive success of polygynous males exceedsthat of monogamous males. These results and those of severalother recent studies are consistent with the assumption thatpolygynous males produce more offspring than monogamous males.     

Behavioral mechanisms preventing filial ovicide in house wrens

Because unmated house wrens (Troglodytes aedon) regularly destroyclutches of conspecifics, we examined mechanisms that preventbreeding individuals from destroying eggs in their own nests.Results of our experimental field study indicate that the egg-destroyingbehavior of males is partially suppressed after mating and thatthe suppression may prevent filial ovicide in some individuals.At least 35% of males continue to destroy conspecific eggs duringthe incubation period of their mates. Because filial ovicideby males is prevented independently of female presence at thenest, we conclude, after eliminating alternative hypotheses,that filial ovicide by males is prevented through their recognitionof nest locations. Egg-destroying behavior of females is alsosuppressed during the incubation. The suppression is strongerthan in males because fewer females than males destroy foreigneggs over a comparable time period. Females respond to experimentallychanged nest location and nest structure, but not egg coloration.We conclude that filial ovicide by females is prevented throughthe suppression of their eggdestroying behavior and throughtheir recognition of nest location and structure.     

Microhabitat heterogeneity influences offspring sex allocation and spatial kin structure in possums

1. Sex allocation theory predicts that where dispersal is sex biased, the fitness consequences of producing male or female offspring are mediated by resource availability and maternal competitive ability. Females in poorer condition are expected to favour dispersing offspring to minimize resource competition with kin. Environmental heterogeneity may drive spatial variation in sex allocation through resource competition-related benefits to females and territory quality benefits to dispersing or philopatric offspring. 2. Here, we demonstrate that microhabitat heterogeneity can drive extremely fine-scale spatial heterogeneity in offspring sex allocation. Female bobucks (Trichosurus cunninghami) in temperate rainforest were more likely to produce male offspring than those in surrounding Eucalyptus forest. 3. A maternal physiological effect was identified, in that females of lower body mass were more likely to produce male offspring. This finding is consistent with resource competition predictions, in that smaller females are expected to have poorer competitive ability. 4. Genetic spatial autocorrelation analysis identified males as the more dispersing sex. Furthermore, overproduction of males by mothers in the rainforest habitat was geographically concordant with reduced philopatry, as inferred from spatial genetic analysis. This provides empirical validation of dispersal-related explanations of offspring sex allocation: that production of offspring of the dispersing sex minimizes the potential for resource competition with kin. 5. Spatial variation in dispersal via sex allocation responses to environmental heterogeneity can potentially contribute to spatial patterns in population dynamics.     

Nonlinear and population-specific offspring sex ratios in relation to high variation in prey abundance

Montagu's harrier ( Circus pygargus ), a specialist raptor in western France, faces huge variations in the abundance of its main prey, the common vole ( Microtus arvalis ). This simple predator–prey system provides fine-tuned data for investigating patterns of sex allocation under environmental variability. We analysed variations in brood sex ratio at fledging (1364 chicks from 451 broods) in two adjacent harrier populations for respectively 16- and 8-year surveys of both the predator and its prey. Overall sex ratio (number of males/total number of offspring) was close to parity (0.513) but this apparent equilibrium resulted in fact from opposite skews in the two populations which differed by almost 10% (0.561 vs 0.464). Brood reduction only is unlikely to produce such a difference in average brood sex ratios. Brood sex ratio of the predator was affected by prey abundance. Contrary to expectations and whatever the population, relatively more offspring of the smaller sex were produced during peak years of the vole cycle but also during poor years, thus providing the first evidence for a nonlinear influence of environmental quality (prey abundance) on sex ratio. Assuming that observed sex ratios in both populations are the result of an adaptive strategy that maximizes harrier reproductive output, we discuss possible origins of the bias and why nonlinearity may be involved in sex ratio adjustment. These results further point out that sex ratio analyses should take into account population characteristics, and more generally, environmental variations both in space and time.     

Do females adjust the sex of their offspring in relation to the breeding sex ratio?

When the adult sex ratio differs between years in local populations, but still is predictable between adjacent years, it has been proposed that the best strategy would be to bias the offspring sex ratio in favour of the rare sex. We tested this hypothesis using a data set of great reed warbler offspring, sexed by molecular techniques, that were collected over 11 breeding seasons at two adjacent reed marshes. Three important assumptions for this hypothesis are fulfilled in the studied great reed warbler population. First, a substantial proportion of great reed warblers are living in small local populations where sex ratio distortions would be sufficiently large and common. Second, breeding adults and their offspring return to breed in the local population to a high degree. Third, females have a possibility to assess the breeding sex ratio before laying their eggs. At our study site, the breeding sex ratio was positively correlated between successive years. However, contrary to our prediction, female great reed warblers seemed not to adjust their offspring sex ratio in relation to the local breeding sex ratio.     

Unequal maternal investment in offspring quality in relation to predation risk

Equal investment within broods does not always maximize parental reproductive value if the reproductive value of some of the young is low. We examined maternal investment in terms of offspring size in relation to the prospects of survival from predation within broods of the shield bug Elasmucha ferrugata Fabr. (Heteroptera; Acanthosomatidae). Shield bug females guard eggs and first instar nymphs against invertebrate predators by covering the clutch with their body and by behaving aggressively towards their enemies. Survival of eggs was not possible without maternal care. When females were allowed to guard their brood, eggs at the periphery were more vulnerable to predators than eggs at the centre. We found that females laid significantly larger eggs in the safest, central part of the clutch. There seems to be an advantage of large nymph size, since when nymphs were reared separately with low food resources, the larger ones were more likely to survive. Larger nymphs were also more likely to push themselves to the safest, central part of the clutch. Females seem to allocate their resources more to the offspring with the highest probability of avoiding predation. Thus our study supports unequal maternal investment within broods of E.ferrugata.     

No evidence for differential maternal allocation to offspring in the house sparrow (Passer domesticus)

We tested the differential maternal allocation hypothesis ina population of house sparrows. We experimentally altered theattractiveness of males by treating them with implants filledwith crystalline testosterone (T) or left empty (C). We subsequentlymonitored maternal investment as a function of male hormonaltreatment and the size of the black patch of feathers on thethroat (i.e., the badge), a sexually selected trait. The differentialallocation hypothesis predicts that females should adjust theirinvestment with respect to the benefits they receive by matingwith an attractive male. Given that both circulating levelsof T and badge size are condition-dependent traits, we expectedthat females mated with T males and/or with large-badged malesshould invest more into current reproduction. Contrary to thisprediction, we found no evidence that suggested differentialmaternal allocation in this population of house sparrows. Femaleinvestment in yolk T, yolk mass, clutch size, chick brooding,and feeding was not affected by male hormonal treatment or bymale badge size. As expected, T males invested less into chickbrooding and feeding. More surprisingly, females did not compensatethe reduced paternal contribution to chick feeding. As a consequence,the breeding success of T pairs was largely reduced comparedwith that of C pairs. The absence of differential allocationin a system in which it could have an adaptive role raises thequestion about the possible constraints or overriding factorsoperating on patterns of reproductive investment in this species.     

Female-biased sex allocation in relation to growth rate of fruit in Erythronium japonicum

Using four populations of the liliaceous perennial Erythronium japonicum, I examined the hypothesis that sex allocation will be female-biased if the duration of sink-limited growth of fruits, during which fruits grow exponentially, is long. I found that all marked fruits in each population had a period of sink-limited growth. Among the four populations, the mean length of sink-limited growth increased, and the mean dry mass ratio of the sum of the corolla and androecium/fruit decreased, in a consistent order. Thus, plants in populations where the duration of sink-limited growth was long allocated relatively more of their resources to their female functions. This result was consistent with the above hypothesis. Received: 21 March 1998 / Accepted: 27 August 1998     

Constrained sex allocation in a parasitoid due to variation in male quality

The theory of constrained sex allocation posits that when a fraction of females in a haplodiploid population go unmated and thus produce only male offspring, mated females will evolve to lay a female-biased sex ratio. I examined evidence for constrained sex ratio evolution in the parasitic hymenopteran Uscana semifumipennis. Mated females in the laboratory produced more female-biased sex ratios than the sex ratio of adults hatching from field-collected eggs, consistent with constrained sex allocation theory. However, the male with whom a female mated affected her offspring sex ratio, even when sperm was successfully transferred, suggesting that constrained sex ratios can occur even in populations where all females succeed in mating. A positive relationship between sex ratio and fecundity indicates that females may become sperm-limited. Variation among males occurred even at low fecundity, however, suggesting that other factors may also be involved. Further, a quantitative genetic experiment found significant additive genetic variance in the population for the sex ratio of offspring produced by females. This has only rarely been demonstrated in a natural population of parasitoids, but is a necessary condition for sex ratio evolution. Finally, matings with larger males produced more female-biased offspring sex-ratios, suggesting positive selection on male size. Because the great majority of parasitic hymenoptera are monandrous, the finding of natural variation among males in their capacity to fertilize offspring, even after mating successfully, suggests that females may often be constrained in the sex allocation by inadequate number or quality of sperm transferred.     

Adaptive allocation of resources and life-history trade-offs in aphids relative to plant quality

The need to allocate a limited amount of energy between different life-history traits is a fundamental assumption in life-history theory. However, it has often turned out to be extremely difficult to measure the competing processes that contribute to costs or benefits for individual organisms. The present investigation begins by analysing how an aphid clonal lineage adapts its reproductive investment to moderate changes in host plant quality (e.g. during the life cycle of its host). Using Centaurea jacea and Uroleucon jaceae as a model plantaphid system, I show that reproductive investment can be far more complex than indicated by dry or wet mass of the gonads alone. The number of embryos of a particular size class or developmental state present in the reproductive system of an aphid is highly flexible and is influenced by the quality of the host plant. Next, the effects of a particular reproductive investment on survival during periods of food deprivation are analysed for aphids originating from host-plants of different qualities. When food stress is severe the ability to rapidly resorb and reallocate resources committed to offspring is important for survival. However, this ability is limited. I argue that, in periods of food stress, young, unsclerotized embryos might serve as a kind of energy buffer similar to a fat body and are therefore not relevant to cost-benefit calculations. However, embryos that are beginning to sclerotize within the ovarioles are not available for resorption and resource reallocation. They compete for nutrients with their mother and contribute to costs. Therefore, it is suggested that the reproductive investment of an aphid should not be equated with reproductive costs in a general al way. The dynamics of adaptive resource allocation and resorption are a key feature of an aphid's life history, and the implications for life-history theory are discussed.     

Evidence for heterozygote instability in microsatellite loci in house wrens

Microsatellite loci have high mutation rates and high levels of allelic variation, but the factors influencing their mutation rate are not well understood. The proposal that heterozygosity may increase mutation rates has profound implications for understanding the evolution of microsatellite loci, but currently has limited empirical support. We examined 20 microsatellite mutations identified in an analysis of 12 260 meiotic events across three loci in two populations of a songbird, the house wren (Troglodytes aedon). We found that for an allele of a given length, mutation was significantly more likely when there was a relatively large difference in size between the allele and its homologue (i.e. a large ‘allele span’). Our results support the proposal of heterozygote instability at microsatellite loci.     

Mothers adjust offspring sex to match the quality of the rearing environment

Theory predicts that mothers should adjust offspring sex ratios when the expected fitness gains or rearing costs differ between sons and daughters. Recent empirical work has linked biased offspring sex ratios to environmental quality via changes in relative maternal condition. It is unclear, however, whether females can manipulate offspring sex ratios in response to environmental quality alone (i.e. independent of maternal condition). We used a balanced within-female experimental design (i.e. females bred on both low- and high-quality diets) to show that female parrot finches (Erythrura trichroa) manipulate primary offspring sex ratios to the quality of the rearing environment, and not to their own body condition and health. Individual females produced an unbiased sex ratio on high-quality diets, but over-produced sons in poor dietary conditions, even though they maintained similar condition between diet treatments. Despite the lack of sexual size dimorphism, such sex ratio adjustment is in line with predictions from sex allocation theory because nutritionally stressed foster sons were healthier, grew faster and were more likely to survive than daughters. These findings suggest that mothers may adaptively adjust offspring sex ratios to optimally match their offspring to the expected quality of the rearing environment.     

Adjustment of offspring sex ratios in relation to the availability of resources for philopatric offspring in the common brushtail possum

The local-resource-competition hypothesis predicts that where philopatric offspring compete for resources with their mothers, offspring sex ratios will be biased in favour of the dispersing sex. This should produce variation in sex ratios between populations in relation to differences in the availability of resources for philopatric offspring. However, previous tests of local resource competition in mammals have used indirect measures of resource availability and have focused on sex-ratio variation between species or individuals rather than between local populations. Here, we show that the availability of den sites predicts the offspring sex ratio in populations of the common brushtail possum. Female possums defend access to dens, and daughters, but not sons, occupy dens within their mother's range. However, the abundances of possums in our study areas were determined principally by food availability. Consequently, in food-rich areas with a high population density, the per-capita availability of dens was low, and the cost of having a daughter should have been high. This cost was positively correlated with male bias in the sex ratio at birth. Low per capita availability of dens was correlated with male bias in the sex ratio at birth.     

Adaptive sex allocation in birds: the complexities of linking theory and practice

We review some recent theoretical and empirical developments in the study of sex allocation in birds. The advent of reliable molecular sexing techniques has led to a sharp increase in the number of studies that report biased offspring sex ratios in birds. However, compelling evidence for adaptive sex allocation in birds is still very scant. We argue that there are two reasons for this: (i) standard sex allocation models, very helpful in understanding sex allocation of invertebrates, do not sufficiently take the complexities of bird life histories and physiology into account. Recent theoretical work might bring us a step closer to more realistic models; (ii) experimental field and laboratory studies on sex allocation in birds are scarce. Recent experimental work both in the laboratory and in the field shows that this is a promising approach.     

Sexual dimorphism,survival, and parental investment in relation to offspring sex in a precocial bird

Differential growth rate between males and females, owing to a sexual size dimorphism, has been proposed as a mechanism driving sex‐biased survival. How parents respond to this selection pressure through sex ratio manipulation and sex‐biased parental investment can have a dramatic influence on fitness. We determined how differential growth rates during early life resulting from sexual size dimorphism affected survival of young and how parents may respond in a precocial bird, the black brant Branta bernicla nigricans. We hypothesized that more rapidly growing male goslings would suffer greater mortality than females during brood rearing and that parents would respond to this by manipulating their primary sex ratio and parental investment. Male brant goslings suffered a 19.5% reduction in survival relative to female goslings and, based on simulation, we determined that a female biased population sex ratio at fledging was never overcome even though previous work demonstrated a slight male‐biased post‐fledging survival rate. Contrary to the Fisherian sex ratio adjustment hypothesis we found that individual adult female brant did not manipulate their primary sex ratio (50.39% male, n = 645), in response to the sex‐biased population level sex ratio. However, female condition at the start of the parental care period was a good predictor of their primary sex ratio. Finally, we examined how females changed their behavior in response to primary sex ratio of their broods. We hypothesized that parents would take male biased broods to areas with increased growth rates. Parents with male biased primary sex ratios took broods to areas with higher growth rates. These factors together suggest that sex‐biased growth rates during early life can dramatically affect population dynamics through sex‐biased survival and recruitment which in turn affects decisions parents make about sex allocation and sex‐biased parental investment in offspring to maximize fitness.     

Adaptive adjustment of offspring sex ratio and maternal reproductive effort in an iteroparous mammal

Large mammals in seasonal environments have a pattern of high-reproductive synchrony in spring, but how the timing of reproduction affects resource allocation decisions at different stages of the reproductive cycle remains largely unexplored. By manipulating the timing of conception in reindeer (Rangifer tarandus), we tested how the timing of conception affected sex ratio, gestation length and weight development of mother and offspring. Females that conceived at their first ovulation within the rut had a 60.5% probability of producing a male; in contrast, females that conceived a cycle later had a 31.3% probability of producing a male. Late conceiving females had gestation times that were 10 days shorter and the calves were 0.6 kg (9.2%) lighter at birth and 7.4 kg (14.7%) lighter in autumn. Over the year, female weight changes was similar between the groups suggesting reindeer follow a bet-hedging strategy; reducing the quality of this year's offspring to ensure their own future reproduction and survival. Harvesting is often selective leading to skewed sex ratios and age structure, which may influence the timing of reproduction due to females hesitation to mate with young males. Whenever this hesitation is strong enough to increase the frequency of recycling, harvesting is likely to have profound life history consequences.