Temperature-dependent sex ratio in a bird

To our knowledge, there is, so far, no evidence that incubation temperature can affect sex ratios in birds, although this is common in reptiles. Here, we show that incubation temperature does affect sex ratios in megapodes, which are exceptional among birds because they use environmental heat sources for incubation. In the Australian brush-turkey Alectura lathami, a mound-building megapode, more males hatch at low incubation temperatures and more females hatch at high temperatures, whereas the proportion is 1:1 at the average temperature found in natural mounds. Chicks from lower temperatures weigh less, which probably affects offspring survival, but are not smaller. Megapodes possess heteromorphic sex chromosomes like other birds, which eliminates temperature-dependent sex determination, as described for reptiles, as the mechanism behind the skewed sex ratios at high and low temperatures. Instead, our data suggest a sex-biased temperature-sensitive embryo mortality because mortality was greater at the lower and higher temperatures, and minimal at the middle temperature where the sex ratio was 1:1.     

Female infanticide and human sex ratio evolution.

The possible effect on the evolution of the human sex ratio of a preference for male children is examined in a genetic model. It is shown that the killing of infant daughters can lead to either a female- or a male-biased sex ratio, the outcome depending on the decision rule used to determine the fate of a child. This reconciles long-standing contradictory results.     

Brood sex ratio variation in a cooperatively breeding bird

In cooperatively breeding species, the fitness consequences of producing sons or daughters depend upon the fitness impacts of positive (repayment hypothesis) and negative (local competition hypothesis) social interactions among relatives. In this study, we examine brood sex allocation in relation to the predictions of both the repayment and the local competition hypotheses in the cooperatively breeding long-tailed tit Aegithalos caudatus. At the population level, we found that annual brood sex ratio was negatively related to the number of male survivors across years, as predicted by the local competition hypothesis. At an individual level, in contrast to predictions of the repayment hypothesis, there was no evidence for facultative control of brood sex ratio. However, immigrant females produced a greater proportion of sons than resident females, a result consistent with both hypotheses. We conclude that female long-tailed tits make adaptive decisions about brood sex allocation.     

Adaptive sex differences in growth of pre-ovulation oocytes in a passerine bird

Maternal modification of offspring sex in birds has strong fitness consequences, however the mechanisms by which female birds can bias sex of their progeny in close concordance with the environment of breeding are not known. In recently established populations of house finches (Carpodacus mexicanus), breeding females lay a sex-biased sequence of eggs when ambient temperature causes early onset of incubation. We studied the mechanisms behind close association of incubation and sex-determination strategies in this species and discovered that pre-ovulation oocytes that produce males and females differed strongly in the temporal patterns of proliferation and growth. In turn, sex-specific exposure of oocytes to maternal secretion of prolactin and androgens produced distinct accumulation of maternal steroids in oocyte yolks in relation to oocyte proliferation order. These findings suggest that sex difference in oocyte growth and egg-laying sequence is an adaptive outcome of hormonal constraints imposed by the overlap of early incubation and oogenesis in this population, and that the close integration of maternal incubation, oocytes' sex-determination and growth might be under control of the same hormonal mechanism. We further document that population establishment and the evolution of these maternal strategies is facilitated by their strong effects on female and offspring fitness in a recently established part of the species range.     

Maternal corticosteroids influence primary offspring sex ratio in a free-ranging passerine bird

When fitness benefits of investment in sons and daughters differ,animals are predicted to manipulate the sex ratio of their offspring.Sex ratio manipulation occurs in many taxa, but the mechanismsunderlying the phenomenon in vertebrates remain largely unknown.Factors favoring skewed sex ratios, such as reduced maternalcondition or food availability, also induce elevated corticosteroids.Recent experimental studies support a causal relationship betweencorticosteroids and sex ratio. Evidence of a natural correlationbetween maternal corticosteroids and offspring sex ratio hasbeen lacking, however. Without such evidence, the importanceof corticosteroids in influencing sex ratios in natural populationswas unknown. We measured baseline corticosteroids in 19 free-rangingfemale white-crowned sparrows (Zonotrichia leucophrys) and thesex ratios of their offspring. Females with high corticosteroidsproduced more daughters than females with low hormone levels.We then conducted a controlled, field-based experiment investigatingthe effects of moderately increased maternal corticosteroidson offspring sex ratios to determine if the observed correlationreflects a causal relationship between maternal corticosteroidsand offspring sex ratio. Hormone-implanted females producedmore female embryos than control females. These findings providethe first evidence of a natural correlation between maternalcorticosteroids and offspring sex ratios in free-ranging birds,and the first experimental evidence of a causal link betweenmoderate increases in corticosteroids and biased primary sexratios.     

Variably male-biased sex ratio in a marine bird with females larger than males

When the costs of rearing males and females differ progeny sex ratios are expected to be biased toward the less expensive sex. Blue-footed booby (Sula nebouxii) females are larger and roughly 32% heavier than males, thus presumably more costly to rear. We recorded hatching and fledging sex ratios in 1989, and fledging sex ratios during the next 5 years. In 1989, the sample of 751 chicks showed male bias at hatching (56%) and at fledging (57% at ˜90 days). Fledging sex ratios during the five subsequent reproductive seasons were at unity (1 year) or male-biased, varying from 56% to 70%. Male bias was greater during years when mean sea surface temperature was warmer and food was presumably in short supply. During two warm-water years (only) fledging sex ratio varied with hatching date. Proportions of male fledglings increased with date from 0.48 to 0.73 in 1994, and from 0.33 to 0.79 in 1995. Similar results were obtained when the analysis was repeated using only broods with no nestling mortality, suggesting that the overall increase in the proportion of males over the season was the result of sex ratio adjustments at hatching. The male-biased sex ratio, and the increased male bias during poor breeding conditions supports the idea that daughters may be more costly than sons, and that their relative cost increases in poor conditions. Received: 3 February 1998 / Accepted: 12 September 1998     

Factors affecting secondary sex ratio in Iranian Holsteins

The objective of this study was to evaluate the factors affecting secondary sex ratio (SSR) in Iranian Holsteins. Data of 942,941 Holstein calving events from the Animal Breeding Center of Iran, recorded between January 1996 and December 2007, were used in the analysis. A multivariable logistic regression model was used to model the logit of the probability of a male calf being born. Male births accounted for 49.6% of the total observations. The ratio of males to females varied from 52.5:47.5 in calving year 1996-1999 (odds ratio (OR) = 1.18; P < 0.0001), to 48.5:51.5 in calving year 2004-2007. The greatest occurrence of male births was observed in spring (OR = 1.02; P < 0.0001), and the lowest incidence of male births was for summer or fall calvings. Also, the frequency of male births decreased from parity 1 to parity 4 and beyond (P < 0.0001; OR = 1.11). The greatest number of sires had the SSR equal to 0.5 with a minimum SSR of 32% while the maximum was 97%. Among cows that had a male birth, the chance of delivering a male calf again was 25.5% when cows had delivered a male once (OR = 1.14; P < 0.0001), and 12.7% if a male calf was delivered twice by a cow. This indicated that characteristics peculiar to the dam influence the sex of her offspring and suggests some degree of repeatability of calf sex within cows.     

Persistence of an extreme male-biased adult sex ratio in a natural population of polyandrous bird

In a number of insects, fishes and birds, the conventional sex roles are reversed: males are the main care provider, whereas females focus on matings. The reversal of typical sex roles is an evolutionary puzzle, because it challenges the foundations of sex roles, sexual selection and parental investment theory. Recent theoretical models predict that biased parental care may be a response to biased adult sex ratios (ASRs). However, estimating ASR is challenging in natural populations, because males and females often have different detectabilities. Here, we use demographic modelling with field data from 2101 individuals, including 579 molecularly sexed offspring, to provide evidence that ASR is strongly male biased in a polyandrous bird with male-biased care. The model predicts 6.1 times more adult males than females (ASR=0.860, proportion of males) in the Kentish plover Charadrius alexandrinus. The extreme male bias is consistent between years and concordant with experimental results showing strongly biased mating opportunity towards females. Based on these results, we conjecture that parental sex-role reversal may occur in populations that exhibit extreme male-biased ASR.     

Gonadotrophin and the human secondary sex ratio.

A review of published reports showed that the sex ratio (proportion of boys) was low among infants conceived after ovulation had been induced. The difference between the observed sex ratio and an expected one of 0 . 514 was highly significant. These findings suggest that maternal gonadotrophin concentrations at the time of conception directly affect the sex of the zygote.     

Temporal trends in the secondary sex ratio in Nordic countries

Attempts have been made to identify factors influencing the number of males per 100 females at birth, also called the secondary sex ratio. It has been proposed to vary inversely with the frequency of prenatal losses, but available data lend at best only weak support for this hypothesis. Statistical analyses have shown that comparisons between secondary sex ratios demand large data sets. Variations in the secondary sex ratio that have been reliably identified in family data have mostly been slight and without a notable influence on national birth registers. For Sweden, 1751-1950, the secondary sex ratio among all births and live births revealed increasing trends. The Swedish results are compared with available findings for live births in Finland, Norway, Denmark, and the small Icelandic population. For Norway and Denmark, the secondary sex ratio increased during 1801-1950. A similar, but stronger pattern was observed for Finland (1751-1950) and Iceland (1838-1950). During the latter half of the twentieth century, marked decreases were observed in all countries. Attempts to identify reliable associations between secondary sex ratios and stillbirth rates have been made, but no consistent results have emerged.     

Impact of economic conditions on the secondary sex ratio in a post-communist economy

According to the Trivers-Willard hypothesis the secondary sex ratio (SSR, the ratio of male to female newborns [M/F]) should be positively related to the parents’ living conditions. This also means that if in some population parents experience environmental (e.g. economic) stress, the SSR should be relatively low. If this holds true, the fluctuations in the SSR of offspring could be one of the ways the human population reacts to environmental (and also socio-economic) changes. Although confirmed for many human populations, such a relationship was not observed in the populations living in the communist-era planned-economy countries until recently. We test the hypothesis that economic stress in Poland after the communist era is also related to the SSR decrease. Using quarterly data from the years 1995-2007 about the total number of live male (M) and female (F) newborns born in central Poland (sample size = 310,532), we calculated the time series of the SSR. The quarterly economic conditions of the studied population within the period under consideration constituted the time series of the percentage change in private consumption at constant prices of the year 2000. The relationship between the SSR and the economic conditions in the analyzed 47 quarters of the year was tested with the use of the ARMA models. We have found that four quarters (one year) after the occurrence of economic stress there was a decline in the SSR. This result is consistent with the Trivers-Willard hypothesis at the population level in a modern free-trade economy of a post-communist country.     

The secondary sex ratio in Israel: 1980-1995

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.