Increased secondary sex ratios in golden hamster litters sired by males without coagulating glands and seminal vesicles

1996 ◽  
Vol 8 (2) ◽  
pp. 297 ◽  
Author(s):  
PH Chow ◽  
MP Cheung ◽  
WS O

In golden hamsters, although bilateral ablation of paternal coagulating glands (CGX) and seminal vesicles (SVX) did not affect fertility, a higher number of male pups were born. The present study aimed at determining whether this male-biased sex ratio was due to an imbalance of fertilization by X and Y chromosome-bearing sperms or whether it was the consequence of a sex-related differential survival of embryos. The sex of embryos sired by sham-operated (SH) controls or males subjected to bilateral ablation of ampullary glands (AGX), CGX and SVX was determined from chromosomal spreads at 10 h post coitum and 10 days post coitum. The primary sex ratio of of the SH group did not deviate from the hypothetical sex ratio of 1:1. The sex ratios of zygotes from the three experimental groups did not differ from that of the controls. However, by mid gestation, the sex ratio was significantly higher in the SVX group (P < 0.05) and the CGX group (P < 0.005). The absence of secretions from the ampullary gland, coagulating gland and seminal vesicle had no effect on the primary sex ratio, thus these glands did not appear to affect fertilization by the X and Y chromosome-bearing sperm. The increased secondary sex ratios observed in the SVX and CGX groups were due to the preferential survival of males.


1997 ◽  
Vol 75 (5) ◽  
pp. 755-770 ◽  
Author(s):  
Maria Ângela Marcovaldi ◽  
Matthew H. Godfrey ◽  
N. Mrosovsky

A method of estimating natural sex ratios of hatchlings of species with temperature-dependent sexual differentiation from data on incubation durations is described. The method was applied to loggerhead turtles (Caretta caretta) nesting in Brazil. Data on incubation durations were collected from 11 nesting beaches monitored for up to six seasons. It was estimated that 82.5% of the loggerhead hatchlings produced were female. The strongly female-biased sex ratio in Brazil is similar to that found previously for loggerheads using beaches in the eastern U.S.A. This suggests that a female-biased hatchling sex ratio may be a feature of loggerhead populations.



Author(s):  
Ryosuke Iritani ◽  
Stuart A West ◽  
Jun Abe

AbstractHamilton’s local mate competition theory provided an explanation for extraordinary female biased sex ratios in a range of organisms. When mating takes place locally, in structured populations, a female biased sex ratio is favoured to reduce competition between related males, and to provide more mates for males. However, there are a number of wasp species where the sex ratios appear to more female biased than predicted by Hamilton’s theory. We investigated theoretically the extent to which cooperative interactions between related females can interact with local mate competition to favour even more female biased sex ratios. We found that: (i) cooperative interactions between females can lead to sex ratios that are more female biased than predicted by local competition theory alone; (ii) sex ratios can be more female biased when the cooperative interactions are offspring helping parents before dispersal, rather than cooperation between siblings after dispersal. Our results can be applied to a range of organisms, and provide an explanation for the extreme sex ratio biases that have been observed in Sclerodermus and Melittobia wasps.



Heredity ◽  
2006 ◽  
Vol 96 (6) ◽  
pp. 464-470 ◽  
Author(s):  
R M Shahjahan ◽  
P A Rendon ◽  
L M Cook ◽  
R J Wood


2019 ◽  
Vol 110 (4) ◽  
pp. 411-421 ◽  
Author(s):  
Fredric J Janzen ◽  
David M Delaney ◽  
Timothy S Mitchell ◽  
Daniel A Warner

Abstract Fisherian sex-ratio theory predicts sexual species should have a balanced primary sex ratio. However, organisms with environmental sex determination (ESD) are particularly vulnerable to experiencing skewed sex ratios when environmental conditions vary. Theoretical work has modeled sex-ratio dynamics for animals with ESD with regard to 2 traits predicted to be responsive to sex-ratio selection: 1) maternal oviposition behavior and 2) sensitivity of embryonic sex determination to environmental conditions, and much research has since focused on how these traits influence offspring sex ratios. However, relatively few studies have provided estimates of univariate quantitative genetic parameters for these 2 traits, and the existence of phenotypic or genetic covariances among these traits has not been assessed. Here, we leverage studies on 3 species of reptiles (2 turtle species and a lizard) with temperature-dependent sex determination (TSD) to assess phenotypic covariances between measures of maternal oviposition behavior and thermal sensitivity of the sex-determining pathway. These studies quantified maternal behaviors that relate to nest temperature and sex ratio of offspring incubated under controlled conditions. A positive covariance between these traits would enhance the efficiency of sex-ratio selection when primary sex ratio is unbalanced. However, we detected no such covariance between measures of these categories of traits in the 3 study species. These results suggest that maternal oviposition behavior and thermal sensitivity of sex determination in embryos might evolve independently. Such information is critical to understand how animals with TSD will respond to rapidly changing environments that induce sex-ratio selection.



Parasitology ◽  
2000 ◽  
Vol 121 (4) ◽  
pp. 379-383 ◽  
Author(s):  
J. BOISSIER ◽  
H. MONÉ

The sex ratio of adult worms has been observed biased towards males in Schistosoma mansoni under natural conditions. The origin of this bias is unknown. This paper determines whether males are more infective than females under controlled experimental bisexual conditions, and hence if the sex ratio is male-biased as a consequence of this. The male and female cercarial infectivities in uni- and bisexual vertebrate host infections using a range of controlled cercarial sex ratios were studied. The results showed that, in experimental unisexual infections, male cercariae were more infective than females, and that in experimental bisexual infections, male cercarial infectivity was similar to that of female, irrespective of cercarial sex ratio. Furthermore, cumulative male and female cercarial infectivity was maximal when sex ratio was equilibrated. The unbiased sex ratios obtained in our experimental bisexual infections are discussed in terms of behavioural and/or biochemical male–female interaction. Alternative explanations of the natural biased sex ratio are proposed.



Genetics ◽  
1994 ◽  
Vol 136 (2) ◽  
pp. 641-651
Author(s):  
D R Taylor

Abstract A survey of maternal families collected from natural populations showed that the sex ratio in Silene alba was slightly female biased. Sex ratio varied among populations and among families within a female biased population. Crosses among plants from the most female biased population and the most male biased population showed that the sex ratio polymorphism was inherited through or expressed in the male parent. Males from one family in particular exhibited a severe female bias, characterized by less than 20% male progeny. The inheritance of sex ratio was investigated using a reciprocal crossing design. Sex ratios from reciprocal crosses were significantly different, indicating either sex-linkage or cytoplasmic inheritance of sex ratio. The sex ratios produced by males generally resembled the sex ratios produced by their male parents, indicating that the sex ratio modifier was Y linked. The maternal parent also significantly influenced sex ratio through an interaction with the genotype of the paternal parent. Sex ratio, therefore, is apparently controlled by several loci. Although sex ratio bias in this species may be due to deleterious alleles on the Y chromosome, it is more likely to involve an interaction between loci that cause the female bias and a Y-linked locus that enhances the proportion of males in the progeny.



2011 ◽  
Vol 86 (4) ◽  
pp. 401-405 ◽  
Author(s):  
S. D'Ávila ◽  
E.C.A. Bessa ◽  
S. Souza-Lima ◽  
M.L.A. Rodrigues

AbstractIn the present study populations of the avian nematode species Baruscapillaria obsignata are described from Columba livia. Male and female individuals were obtained from 27 birds, fixed in alcohol/formalin/acetic acid (AFA) and preserved in 70% ethanol. Nematodes were identified and then counted under a stereoscopic microscope. Baruscapillaria obsignata were much more frequent in the anterior third of the small intestine, and females were more abundant than males in all infra populations. The prevalence was 55.6%, mean intensity was 11.8 (median 11.0; range 1–31) and abundance 6.56. In the present study, we observed an aggregated distribution of parasite infrapopulations, as demonstrated by the value of the exponent of the negative binomial distribution, K = 0.2773; by the discrepancy index, D = 0.656 and by the variance/mean ratio, 12.44. The female/male sex ratios found in all infrapopulations were always greater than 1, showing a bias in favour of female abundance. This tendency was especially marked in infrapopulations containing fewer individuals. The sizes of infrapopulations ranged from 5 to 31 individuals. The mean sex ratio observed was 2.69 ± 3.28 (median 1.83; range 0–11). In infrapopulations with 5–15 individuals, the sex ratios observed varied from 2.6 to 11, while in those with 17–31 individuals, the sex ratios were lower, ranging from 1.7 to 2.4. There was a negative correlation between the intensity of infection and the sex ratio of infrapopulations. Results are discussed in terms of possible factors influencing the processes that lead to niche restriction and biased sex ratios in parasite infrapopulations.



1992 ◽  
Vol 70 (3) ◽  
pp. 530-538 ◽  
Author(s):  
N. Mrosovsky ◽  
Jane Provancha

Hatchling loggerhead sea turtles (Caretta caretta) were collected over three nesting seasons from a rookery at Cape Canaveral, Florida. From data on the distribution of nests over the season, we estimated that 92.6–96.7, 94.7–99.9, and 87.0–89.0% of the hatchlings produced on this beach in 1986, 1987, and 1988, respectively, were females. These skewed sex ratios were consistent with the fact that for most of the season, sand temperatures were above the pivotal level for loggerhead turtles. The present results show that the female-biased sex ratio reported previously by these authors for the 1986 nesting season at this site was not an isolated, atypical event. In addition to a total of 3 years of sampling for sex ratio, measurements of beach temperatures at the depth of turtle nests were extended to cover 5 years. These temperatures were commonly above the pivotal level. The strongly female-biased hatchling sex ratio found in this population of loggerhead turtles poses theoretical challenges. It may also complicate conservation efforts, since global warming might be expected to skew the sex ratio still further toward females.



Genetics ◽  
1992 ◽  
Vol 131 (1) ◽  
pp. 155-161 ◽  
Author(s):  
F J Janzen

Abstract The magnitude of quantitative genetic variation for primary sex ratio was measured in families extracted from a natural population of the common snapping turtle (Chelydra serpentina), which possesses temperature-dependent sex determination (TSD). Eggs were incubated at three temperatures that produced mixed sex ratios. This experimental design provided estimates of the heritability of sex ratio in multiple environments and a test of the hypothesis that genotype x environment (G x E) interactions may be maintaining genetic variation for sex ratio in this population of C. serpentina. Substantial quantitative genetic variation for primary sex ratio was detected in all experimental treatments. These results in conjunction with the occurrence of TSD in this species provide support for three critical assumptions of Fisher's theory for the microevolution of sex ratio. There were statistically significant effects of family and incubation temperature on sex ratio, but no significant interaction was observed. Estimates of the genetic correlations of sex ratio across environments were highly positive and essentially indistinguishable from + 1. These latter two findings suggest that G x E interaction is not the mechanism maintaining genetic variation for sex ratio in this system. Finally, although substantial heritable variation exists for primary sex ratio of C. serpentina under constant temperatures, estimates of the effective heritability of primary sex ratio in nature are approximately an order of magnitude smaller. Small effective heritability and a long generation time in C. serpentina imply that evolution of sex ratios would be slow even in response to strong selection by, among other potential agents, any rapid and/or substantial shifts in local temperatures, including those produced by changes in the global climate.



2020 ◽  
Author(s):  
Thomas Richardson

The operational sex ratio has been shown to influence a variety of behaviours in humans and non-human animals, particularly relating to intrasexual competition. One way females compete for mates is by derogating other women’s attractiveness. Recent studies have shown that priming participants with different sex ratios can induce sex ratio effects on behaviour. In a pre-registered, double blind experiment, 71 single women came to the lab twice and were primed with either a favourable (many men) or unfavourable (few men) sex ratio. I assessed whether unfavourable sex ratios increased self reported intrasexual competitiveness, as well as competitor derogation in the form of decreased ratings of female facial attractiveness and kindness. I also assessed whether they expressed less choosiness by rating male faces as more attractive. I tested whether any sex ratio effects are weaker for more attractive women. Finally, I attempted to replicate previous work suggesting that a male biased sex ratio increases women's preference for their future career over their future family. Despite having higher statistical power than most previous studies of this type, I did not find evidence for any of the hypothesised effects and failed to replicate 2 previous findings. The data indicated that the sex ratio manipulation likely did not work.



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