No evidence of temperature-dependent sex determination or sex-biased embryo mortality in the chicken.

Skewing the sex ratio at hatch in commercial poultry would be economically beneficial to the poultry industry. The existence of temperature-dependent sex determination is uncertain in birds. This experiment investigated if incubation temperatures skew sex ratios of commercial broilers. Three incubators were each set at a hot (38.3°C), standard (37.5°C), or cool (36.7°C) single-stage incubation temperature one time over 3 trials to eliminate incubator effect as a Latin square design. Sex ratios of hatched chicks and dead embryos were monitored. In one trial, embryo weights were evaluated. The percentages of male hatched chicks did not differ based on incubation temperature (P = 0.4486; 49.5% in the hot treatment, 51.4% at standard temperature, and 49.8% in the cool treatment). The percent hatch of eggs set was lower in the hot treatment (83.6%) than the standard (93.5%) and cool (91.6%) treatments (P < 0.0001) with greater late embryonic mortality in the hot treatment (P < 0.0001); however, the sex ratio of dead embryos did not differ among treatments (P = 0.9863). Pooled data of embryo mortality found no sex-biased embryo mortality with a female/male sex ratio of 1.22:1 (χ(2) = 1.27; P = 0.2596). Embryos from the hot treatment were heavier than those from the standard treatment by d 14 of incubation and were heavier than the embryos from the cool treatment by d 9 of incubation (P < 0.0001). These data indicate that incubation temperature affects embryonic mortality and embryonic growth rate, but it does not affect the sex ratio of broiler chickens. Additionally, no evidence was found for sex-biased embryo mortality in commercial broilers even at the incubation temperatures of this study.

Steroid hormone content of seminal plasma influences fertilizing ability of sperm in White Leghorns.

Maternal and paternal influences before fertilization can significantly affect the ultimate reproductive output. In avian species, previous studies have shown that concentrations of testosterone (T) in seminal plasma vary greatly and are related to sperm quality. To our knowledge, the presence of other reproductive hormones in avian seminal plasma and their potential influences on fertility remain unstudied. We measured the concentrations of progesterone (P4), T, dihydrotestosterone, and estrogen in seminal and blood plasma collected from White Leghorn roosters. Progesterone was the most abundant hormone compared with all others measured, and concentrations of P4 in seminal plasma were significantly higher than concentrations found in circulation. Given the relatively high concentration of seminal plasma P4, we then attempted to determine its effect on fertility. Hens were inseminated with semen samples that were supplemented with either a high physiological dose of P4 or a control vehicle. Fertilization ability of all semen samples was then characterized using a perivitelline sperm hole penetration assay. Progesterone treatment significantly decreased the ability of sperm to reach and penetrate the egg, suggesting that males that deposit more P4 into seminal plasma may have a decreased capability to fertilize an egg.

Yolk and albumen corticosterone concentrations in eggs laid by white versus brown caged laying hens.

Maternal stress in birds can have permanent transgenerational effects through the transmission of stress hormones to offspring via the egg yolk. Previous studies have shown that White Leghorn hens show a heightened response to stress compared with Hy-Line Brown hens, producing significantly more corticosterone and displaying longer bouts of tonic immobility after handling, whereas baseline levels of corticosterone are similar between the strains. We tested the hypothesis that higher stress responsiveness would correspond to chronic accumulation and thus higher concentrations of corticosterone in egg yolks after exposure to stressors associated with routine maintenance. Eggs were collected from white and brown hens that were undisturbed except for daily feeding and routine egg collections. Corticosterone was quantified in plasma, egg yolks, and albumen and compared between strains. We predicted that corticosterone concentrations in yolk would be higher in eggs from white versus brown hens but that albumen corticosterone would not differ between strains due to the short term of albumen deposition. As predicted, yolk corticosterone concentrations were significantly higher in eggs produced by white hens, approximately twice those found in eggs laid by brown hens. Plasma and albumen concentrations of corticosterone were similar between groups. These results suggest that offspring hatching from eggs laid by White Leghorn hens are exposed to significantly more corticosterone through concentration in the egg yolk, which could permanently imprint offspring physiology and behavior.

Evolution of sex-biased maternal effects in birds: III. Adjustment of ovulation order can enable sex-specific allocation of hormones, carotenoids, and vitamins.

Overlap in growth of offspring should constrain the opportunity for sex-biased maternal effects, yet sex-specific allocation of maternal resources among simultaneously growing ova is often observed in vertebrates. In birds, such allocation can be accomplished either by temporal clustering of ova that become the same sex, resulting in sex-biased egg-laying order, or by follicle-specific delivery of maternal resources. Two house finch populations at the northern and southern boundaries of the species range have opposite ovulation sequences of male and female eggs, and thus, in the absence of sex differences in ova growth or sex-specific maternal strategies, would be expected to have opposite sex-specific accumulation of maternal products. We found that the populations had strong and similar gradients of steroid distribution in relation to ovulation order, whereas distribution of carotenoids and vitamins correlated with each follicle's accumulation of steroids. In both populations, temporal bias in production of sons and daughters within a clutch enabled strongly sex-specific acquisition of maternal products, and oocytes of the same sex were highly interdependent in their accumulation of steroids. Moreover, in nests where the sex-bias in relation to ovulation order deviated from population-specific patterns, eggs had highly distinct concentrations of steroids, carotenoids and vitamins. These results and previous findings of sex-specific yolk partitioning among oocytes suggest that oocytes that become males and females are temporally or spatially clustered during their ovarian growth. We discuss the implication of these findings for the evolution of sex-specific maternal resource allocation.