Post-implantation development of mouse androgenetic embryos produced by in-vitro fertilization of enucleated oocytes.
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We report here on the precise ability of mouse androgenetic embryos produced by in-vitro fertilization of enucleated oocytes to develop to day 9.5 of gestation when cultured with M16 and CZB media. Androgenetic embryos cultured with CZB rather than M16 medium developed to the blastocyst stage in a more significant proportion (56.6% versus 45.0%, P < 0.001). However, after cavitation, the rate of cell proliferation of androgenetic embryos cultured with CZB medium was significantly decreased (P < 0.05). Embryo transfer experiments showed that blastocysts cultured with M16 medium were superior to those cultured with CZB medium in their ability to develop to 9.5-day-old fetuses (28.1% versus 11.1%, P < 0.001). These results showed that the present procedure for producing androgenetic mouse embryos is reliable and that M16 medium is superior for culturing the embryos. Fetal sexing by polymerase chain reaction (PCR) also demonstrated that both XX and XY embryos develop to 9.5-day fetuses at theoretical rates (1:2). This is the first finding that mouse XX androgenones survive after implantation. (+info)
Single-locus complementary sex determination in Diadegma chrysostictos (Gmelin) (Hymenoptera: Ichneumonidae).
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Following the establishment of isofemale lines and subsequent inbreeding, the ichneumonid parasitoid wasp Diadegma chrysostictos (Gmelin) was shown by segregation of polymorphic alloenzyme loci to have single-locus complementary sex determination (sl-CSD). This and the biparental nature of diploid males was confirmed using two independent Mendelian recessive phenotypic markers. The existence of diploid males, sl-CSD, and the abrogation of diploid males following outbreeding was further confirmed by flow cytometry, a potentially general method that is independent of the maternal sex allocation or the need for genetic markers. Estimates of the number of sex alleles in several British populations demonstrated 17-19 alleles in Britain, with a decline toward the northerly limit of the parasitoid's range, varying from 16 in the south of England to 4-5 in central Scotland, in broad agreement with the rate of attainment of a male-biased sex ratio when used to establish en masse laboratory cultures. These data represent the second confirmation of the existence of sl-CSD in the Ichneumonidae (and the first in the Campopleginae subfamily), lending further support to the notion that sl-CSD was the ancestral condition in the Aculeata/Ichneumonoidea clade (Cook 1993a; Periquet et al. 1993). (+info)
Secular movements in sex ratios of adults and of births in populations during the past half-century.
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There is some evidence for a small overall negative correlation across populations between sex ratio (proportion male) at birth and adult sex ratio. There seems to be no systematic correlation within populations across time of sex ratio at birth with adult sex ratio during the past 50 years. So even if adult sex ratios play some part in determining the overall level of the sex ratio at birth, they apparently have played little role in the recent widespread secular changes in sex ratio at birth. It is shown here that there is a strong cohort effect in adult sex ratios: if a woman is in a marriage squeeze (i.e. in a cohort with a relative abundance of women) at age 15 years, she will remain in such a squeeze for the rest of her reproductive life. In England and Wales, the maternal age-specific sex ratios at birth moved roughly in parallel across time during the years 1950-1995. This suggests that sex ratio at birth is not a cohort phenomenon (as it would be if it were affected by adult sex ratio) but is subject to some agents which change with time and affect women (parents) of all ages roughly equally. (+info)
The variation of the probability of a son within and across couples.
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It is suggested that there is a flaw in the currently accepted account of the variation of P, the probability of a boy, within and across couples. It was previously suggested that P has a mean (for Caucasian couples) of approximately 0.514 with an SD of approximately 0.05 across couples: and that the variation within couples is rather less. Grounds are offered here for suspecting that this formulation underestimates both SDs by a factor of as much as 4. It is suggested that in estimating these sources of variation, earlier workers did not consider the possibility that within-couple variation might be random and substantial. In view of the established epidemiology of human sex ratios, it now seems likely that such variation exists, and that there is a substantial measure of counterbalancing across-couple variation. (+info)
Intensity of nest defence is related to offspring sex ratio in the great tit Parus major.
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Nest-defence behaviour of passerines is a form of parental investment. Parents are selected, therefore, to vary the intensity of their nest defence with respect to the value of their offspring. Great tit, Parus major, males were tested for their defence response to both a nest predator and playback of a great tit chick distress call. The results from the two trials were similar; males gave more alarm calls and made more perch changes if they had larger broods and if they had a greater proportion of sons in their brood. This is the first evidence for a relationship between nest-defence intensity and offspring sex ratio. Paternal quality, size, age and condition, lay date and chick condition did not significantly influence any of the measured nest-defence parameters. (+info)
Sex-ratio optimization with helpers at the nest.
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In many cooperatively breeding animals, offspring produced earlier in life assist their parents in raising subsequent broods. Such helping behaviour is often confined to offspring of one sex. Sex-allocation theory predicts that parents overproduce offspring of the helping sex, but the expected degree of sex-ratio bias was thought to depend on specific details of female and male life histories, hampering empirical tests of the theory. Here we demonstrate the following two theories. (i) If all parents produce the same sex ratio, the evolutionarily stable sex ratio obeys a very simple rule that is valid for a general class of life histories. The rule predicts that the expected sex-ratio bias depends on the product of only two parameters which are relatively easily measured: the average number of helping offspring per nest and the relative contribution to offspring production per helper. (ii) If the benefit of helping varies between parents, and parents facultatively adjust the sex ratio accordingly, then the population sex ratio is not necessarily biased towards the helping sex. For example, in line with empirical evidence, if helpers are produced under favourable conditions and parents do not adjust their clutch size to the number of helpers, then a surplus of the non-helping sex is expected. (+info)
The Bateman gradient and the cause of sexual selection in a sex-role-reversed pipefish.
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As a conspicuous evolutionary mechanism, sexual selection has received much attention from theorists and empiricists. Although the importance of the mating system to sexual selection has long been appreciated, the precise relationship remains obscure. In a classic experimental study based on parentage assessment using visible genetic markers, more than 50 years ago A. J. Bateman proposed that the cause of sexual selection in Drosophila is 'the stronger correlation, in males (relative to females), between number of mates and fertility (number of progeny)'. Half a century later, molecular genetic techniques for assigning parentage now permit mirror-image experimental tests of the 'Bateman gradient' using sex-role-reversed species. Here we show that, in the male-pregnant pipefish Syngnathus typhle, females exhibit a stronger positive association between number of mates and fertility than do males and that this relationship responds in the predicted fashion to changes in the adult sex ratio. These findings give empirical support to the idea that the relationship between mating success and number of progeny, as characterized by the Bateman gradient, is a central feature of the genetic mating system affecting the strength and direction of sexual selection. (+info)
Declining male births with increasing geographical latitude in Europe.
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OBJECTIVE: Demographic studies in various industrialised countries have shown a decline in male births in the latter half of the 20th century from the expected ratio of 0.515 (males/total). This study analyses trends in this ratio over the period 1890 to 1995 in Malta, and also analyses this ratio for Western European countries for the period 1990-1995. DESIGN: Births subdivided by sex were obtained from official Maltese publications. European countries were grouped according to geographical latitude by banding countries into three groups: Northern Mediterranean, Central European and Scandinavian. Births by sex for these countries were also analysed for the period 1990-1995. RESULTS: No decline in the ratio of male births to total births was noted in Malta over the period 1916-1995. However, the ratio was higher than expected (n = 151,766, ratio = 0.517 (95% confidence intervals (95% CI): 0.514, 0.519). Moreover, during the period 1890-1899 (n = 66,874), the ratio was 0.523 (95% CI: 0.519, 0.527), even higher than observed during the 20th century (chi 2 = 8.3, p = 0.004). Analysis of European births showed a much higher ratio of male births in the south of Europe than in the north (chi 2 = 87.2, p < 0.0001). CONCLUSIONS: The findings were unable to explain the higher incidence of male births in the south of Europe, but it is speculated that ambient temperatures may not only affect fertility, but also influence sex ratios at birth. (+info)