Do histocompatibility genes influence sex ratio (% males)?

1991 ◽  
Vol 3 (3) ◽  
pp. 267 ◽  
Author(s):  
WG Beamer ◽  
WK Whitten
Keyword(s):  
Sex Ratio ◽  
Sex Ratios ◽  
Strain Differences ◽  
Male Offspring ◽  
Mouse Strains ◽  
Primary Sex Ratio ◽  
Human Male ◽  
Female Survival ◽  
Mendelian Expectation

Breeding records for 15 of the 42 C57BL/10SnJ Congenic Histocompatibility Mouse Strains from the Special Mouse Stocks Resource (SMSR) showed three with a significant excess of male offspring. Strain B10.R111(71NS), hereafter R, gave the highest proportion of males (55.68 +/- 0.59% of 7129 newborn) which is significantly more than the proportion of male offspring (49.81 +/- 0.94% of 2853 newborn) from the C57BL/10SnJ progenitor strain, hereafter B. All mice in the SMSR colonies were fed Old Guildford 96 and Old Guildford 96W liberally on alternate weeks. Breeding females of B and R strains were established in a research colony at the Jackson Laboratory under conditions similar to those in SMSR except that they were fed Wayne Sterilizable Rodent Blox. More than 5000 inbred, hybrid and backcross fetuses were examined but no evidence of an excess of males was found. Also, there were no strain differences in the neonatal data. However, the sex ratio of the 4396 neonates was just significantly higher (P less than 0.05) than that of the fetuses, indicating some perinatal loss of females. An even greater loss of females was most probably the cause of the high sex ratios in the preliminary and follow-up surveys of SMSR R mice, which we ascribe to an interaction between the H-2 haplotype of the R strain, or a gene linked thereto, and the Old Guildford diet that is unfavourable to female survival. The sex ratio of fetuses agreed so closely with the Mendelian expectation as to indicate that the primary sex ratio was 50% males and that the R strain is not a model for the human male bias. There were no hermaphrodites or twins and the sex ratio of the fetuses in litters without resorptions was normal. These findings emphasize the variability of presumptive secondary sex ratios.

scholarly journals BROODSTOCK SEX RATIO IMPROVES FRY PRODUCTION IN NILE TILAPIA(OREOCHROMIS NILOTICUS) IN NORTHERN SENEGAL

2021 ◽  
Vol 9 (02) ◽  
pp. 72-76
Author(s):  
Mouhamadou Amadou Ly ◽  
◽  
Abdoulaye Ngom ◽  
Ahmadou Bamba Fall ◽  
Ousmane Diouf ◽  
...  
Keyword(s):  
Sex Ratio ◽  
Oreochromis Niloticus ◽  
Nile Tilapia ◽  
Sex Ratios ◽  
Survival Rates ◽  
Fish Farming ◽  
Commercial Diet ◽  
Ph Values ◽  
Nile Tilapia Oreochromis Niloticus ◽  
Female Survival

This present study was conducted to determine fry production in different male-female sex ratios of Oreochromis niloticusbroodstock in order to improve fry production, which handicapped the development of fish farming in northern Senegal. A total of 180 broodfish (47 males and 133 females) were stocked at a density of 2 fish /m2and was replicated three times for each sex ratio of 1:2, 1:3and 1:4 (male : female). Mean body weight ranges from 136.47±2.13 and 107.27±2.14 g for female and male O. niloticusbroodstock, respectively. The experiment was conducted for 90 days and the broods were fed on commercial diet containing 32% crude protein.Fish were held in 9 rectangular tanks of 30 m3 each (10 × 3 × 1) and half-filled. The results showed that number of fry produced at different sex ratios were significantly different, with sex ratio of 1:2 producing a highest number of fry (279.67) per female, followed by the 1:3and 1:4 treatment recorded the lowest.Broodstock sex ratios also did not affect female survival rates and all treatments had 100% survival rates. Temperature, dissolved oxygen and pH values obtained were suitable for good water quality and normal tilapia reproduction.In conclusion, the results of the present study recommend to stock Oreochromis niloticus brooders when stocked at a density of 2 fish /m2 at a sex ratio of 1 male : 2 female in order to obtain the highest fry production.

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
Keyword(s):  
Sex Ratio ◽  
Y Chromosome ◽  
Sex Ratios ◽  
Seminal Vesicles ◽  
Differential Survival ◽  
Bilateral Ablation ◽  
Primary Sex Ratio ◽  
Sh Group ◽  
Biased Sex Ratio ◽  
Coagulating Gland

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.

scholarly journals Do Covariances Between Maternal Behavior and Embryonic Physiology Drive Sex-Ratio Evolution Under Environmental Sex Determination?

2019 ◽  
Vol 110 (4) ◽  
pp. 411-421 ◽  
Author(s):  
Fredric J Janzen ◽  
David M Delaney ◽  
Timothy S Mitchell ◽  
Daniel A Warner
Keyword(s):  
Sex Ratio ◽  
Sex Determination ◽  
Environmental Conditions ◽  
Oviposition Behavior ◽  
Thermal Sensitivity ◽  
Sex Ratios ◽  
Theoretical Work ◽  
Environmental Sex Determination ◽  
Turtle Species ◽  
Primary Sex Ratio

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.

scholarly journals Heritable variation for sex ratio under environmental sex determination in the common snapping turtle (Chelydra serpentina).

Genetics ◽  
1992 ◽  
Vol 131 (1) ◽  
pp. 155-161 ◽  
Author(s):  
F J Janzen
Keyword(s):  
Genetic Variation ◽  
Sex Ratio ◽  
Sex Determination ◽  
Sex Ratios ◽  
Chelydra Serpentina ◽  
Heritable Variation ◽  
Snapping Turtle ◽  
Primary Sex Ratio ◽  
Quantitative Genetic ◽  
The Common

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.

Secondary sex ratio of the cyclic parthenogen Daphnia magna (Crustacea: Cladocera) in the Canadian Arctic

1986 ◽  
Vol 64 (5) ◽  
pp. 1137-1143 ◽  
Author(s):  
David M. Barker ◽  
Paul D. N. Hebert
Keyword(s):  
Sex Ratio ◽  
Daphnia Magna ◽  
Sex Ratios ◽  
Canadian Arctic ◽  
Male Offspring ◽  
Environmental Cues ◽  
Environmental Cue ◽  
A Value ◽  
Secondary Sex Ratio ◽  
Ratio Response

Secondary sex ratios of the cyclic parthenogen Daphnia magna were studied in habitats near Churchill, Manitoba. Daphnia magna is believed to possess an environmentally mediated sex-determining system. Throughout the season females produced broods that were predominantly unisexual. The proportion of male offspring was low early in the season but rose to a value near 50% in each of four populations. It is hypothesized that after they have an initial series of female broods, individual females begin to alternate the sexes of their broods in response to an environmental cue. Such an alternation of brood sexes would explain the population sex-ratio pattern observed and would satisfy theoretical requirements for population and individual secondary sex ratios of 1:1. In studies on cladocerans, environmental cues inducing the sex-ratio response must be distinguished from cues with a sex-determining effect.

scholarly journals Effect of manipulated sex ratio on insemination of the red mason bee Osmia bicornis L. under net cage conditions

2013 ◽  
Vol 57 (2) ◽  
pp. 73-79 ◽  
Author(s):  
Monika Fliszkiewicz ◽  
Aleksandra Langowska ◽  
Piotr Tryjanowski
Keyword(s):  
Sex Ratio ◽  
Plant Breeding ◽  
Sperm Count ◽  
Sex Ratios ◽  
Natural Populations ◽  
Osmia Bicornis ◽  
Strong Interest ◽  
Female Survival ◽  
Net Cage ◽  
Fruit Plants

Abstract The red mason bee Osmia bicornis L. (Hymenoptera: Megachilidae) is a solitary gregarious species that is known to be a good pollinator of pear, apple, and several other Rosaceae fruit plants. Mainly females are active in plant pollination, and therefore they are of strong interest to farmers. As natural populations are usually male biased, here we studied the possibility of rearing a female-biased population of Osmia bicornis by examining the effects of sex ratio changes on female survival, insemination rate, and sperm count in the spermatheca. Using bees that had completed their winter diapause and were maintained in flying cages, we created three groups with different male:female sex ratios: 1:1, 1:2, and 1:3. The 1:3 sex-ratio group exhibited the best survival of females, but the lowest spermathecae sperm count. The insemination rate did not differ between groups. Our results indicate that-at least among bees housed in isolator cages for plant breeding- skewing the sex ratio towards more females does not affect bee survival, and efficient insemination can be expected with twice as many females as males.

scholarly journals Sex-specific deaths in Norway and Sweden during the COVID-19 pandemic: Did mandates make a difference?

2021 ◽  
pp. 140349482110100
Author(s):  
Ralph Catalano
Keyword(s):  
Sex Ratio ◽  
Infection Control ◽  
Temporal Variation ◽  
Risky Behavior ◽  
Control Strategies ◽  
Sex Ratios ◽  
Female Mortality ◽  
All Cause Mortality ◽  
Societal Expectations ◽  
Male To Female

Aims: To determine whether differences between Norway’s and Sweden’s attempts to contain SARS-CoV-2 infection coincided with detectably different changes in their all-cause mortality sex ratios. Measuring temporal variation in the all-cause mortality sex ratio before and during the pandemic in populations exposed to different constraints on risky behavior would allow us to better anticipate changes in the ratio and to better understand its association with infection control strategies. Methods: I apply time Box–Jenkins modeling to 262 months of pre-pandemic mortality sex ratios to arrive at counterfactual values of 10 intra-pandemic ratios. I compare counterfactual to observed values to determine if intra-pandemic ratios differed detectably from those expected as well as whether the Norwegian and Swedish differences varied from each other. Results: The male to female mortality sex ratio in both Norway and Sweden increased during the pandemic. I, however, find no evidence that the increase differed between the two countries despite their different COVID-19 containment strategies. Conclusion: Societal expectations of who will die during the COVID-19 pandemic will likely be wrong if they assume pre-pandemic mortality sex ratios because the intra-pandemic ratios appear, at least in Norway and Sweden, detectably higher. The contribution of differences in policies to reduce risky behavior to those higher ratios appears, however, small.

scholarly journals Sex Ratios in a Warming World: Thermal Effects on Sex-Biased Survival, Sex Determination, and Sex Reversal

2021 ◽  
Vol 112 (2) ◽  
pp. 155-164
Author(s):  
Suzanne Edmands
Keyword(s):  
High Temperature ◽  
Sex Ratio ◽  
Sex Determination ◽  
Heat Tolerance ◽  
Sex Ratios ◽  
Sex Reversal ◽  
Survival Sex ◽  
Ratio Distortion ◽  
Warming World ◽  
Sex Ratio Distortion

Abstract Rising global temperatures threaten to disrupt population sex ratios, which can in turn cause mate shortages, reduce population growth and adaptive potential, and increase extinction risk, particularly when ratios are male biased. Sex ratio distortion can then have cascading effects across other species and even ecosystems. Our understanding of the problem is limited by how often studies measure temperature effects in both sexes. To address this, the current review surveyed 194 published studies of heat tolerance, finding that the majority did not even mention the sex of the individuals used, with &lt;10% reporting results for males and females separately. Although the data are incomplete, this review assessed phylogenetic patterns of thermally induced sex ratio bias for 3 different mechanisms: sex-biased heat tolerance, temperature-dependent sex determination (TSD), and temperature-induced sex reversal. For sex-biased heat tolerance, documented examples span a large taxonomic range including arthropods, chordates, protists, and plants. Here, superior heat tolerance is more common in females than males, but the direction of tolerance appears to be phylogenetically fluid, perhaps due to the large number of contributing factors. For TSD, well-documented examples are limited to reptiles, where high temperature usually favors females, and fishes, where high temperature consistently favors males. For temperature-induced sex reversal, unambiguous cases are again limited to vertebrates, and high temperature usually favors males in fishes and amphibians, with mixed effects in reptiles. There is urgent need for further work on the full taxonomic extent of temperature-induced sex ratio distortion, including joint effects of the multiple contributing mechanisms.

scholarly journals Sex Chromosome Meiotic Drive in Stalk-Eyed Flies

Genetics ◽  
1997 ◽  
Vol 147 (3) ◽  
pp. 1169-1180 ◽  
Author(s):  
Daven C Presgraves ◽  
Emily Severance ◽  
Gerald S Willrinson
Keyword(s):  
Sex Ratio ◽  
Sex Chromosome ◽  
Sex Ratios ◽  
Natural Populations ◽  
Meiotic Drive ◽  
Operational Sex Ratio ◽  
Genetic Modifiers ◽  
Ratio Distortion ◽  
The Impact ◽  
Sex Ratio Distortion

Meiotically driven sex chromosomes can quickly spread to fixation and cause population extinction unless balanced by selection or suppressed by genetic modifiers. We report results of genetic analyses that demonstrate that extreme female-biased sex ratios in two sister species of stalk-eyed flies, Cyrtodiopsis dalmanni and C. whitei, are due to a meiotic drive element on the X chromosome (Xd). Relatively high frequencies of Xd in C. dalmanni and C. whitei (13–17% and 29%, respectively) cause female-biased sex ratios in natural populations of both species. Sex ratio distortion is associated with spermatid degeneration in male carriers of Xd. Variation in sex ratios is caused by Y-linked and autosomal factors that decrease the intensity of meiotic drive. Y-linked polymorphism for resistance to drive exists in C. dalmanni in which a resistant Y chromosome reduces the intensity and reverses the direction of meiotic drive. When paired with Xd, modifying Y chromosomes (Ym) cause the transmission of predominantly Y-bearing sperm, and on average, production of 63% male progeny. The absence of sex ratio distortion in closely related monomorphic outgroup species suggests that this meiotic drive system may predate the origin of C. whitei and C. dalmanni. We discuss factors likely to be involved in the persistence of these sex-linked polymorphisms and consider the impact of Xd on the operational sex ratio and the intensity of sexual selection in these extremely sexually dimorphic flies.

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