Sex-ratio bias across populations of a freshwater turtle (Testudines : Chelidae) with genotypic sex determination

2006 ◽  
Vol 33 (6) ◽  
pp. 475 ◽  
Author(s):  
Arthur Georges ◽  
Fiorenzo Guarino ◽  
Melissa White

Adult sex ratios vary considerably among populations of single species and across years, but the best evidence is drawn from species with temperature-dependent sex determination. It is difficult to disentangle the effects of bias in the production of the sexes and the effects of a range of other factors contributing to biased adult sex ratios. In this paper, we survey sex ratios across populations of a species constrained to produce 1 : 1 offspring sex ratios by genotypic sex determination and show considerable variation in adult sex ratios. Raw adult sex ratios of Emydura macquarii emmottii were significantly biased in nine of the 11 populations examined. In all but one case, the bias was strongly in favour of males. Part of the bias in sex ratio was attributed to the differing ages of maturity of males and females – males mature younger than females – which leads to more male cohorts being included in the calculations of sex ratio than female cohorts. However, correcting for this effect brought the sex ratios of the populations closer to parity, as expected, and accounted for an overall 62% of the male surplus evident in the adult sex ratio. Even so, it was insufficient to explain the strong male bias (1.2–2.9) in five of the nine populations initially showing such bias. This provides support to those who advise caution in interpreting adult sex ratio data for freshwater turtles in the context of demography, sex allocation or evaluating the impact of climate change.

1989 ◽  
Vol 67 (5) ◽  
pp. 1279-1284 ◽  
Author(s):  
J. Servan ◽  
P. Zaborski ◽  
M. Dorizzi ◽  
C. Pieau

Adult sex ratio in the turtle Emys orbicularis was determined in populations from seven ponds in Brenne (Indre, France). In all populations, the sex ratio was biased toward females. Among 290 captured animals, the male:female ratio was close to 0.5. Among different demographic factors that could affect the adult sex ratio, the most influential was probably the sex ratio of hatchlings. In Emys orbicularis, a ZZ male/ZW female system of genotypic sex determination has been postulated. Moreover, gonad differentiation is dependent on temperature and sex-reversed individuals can occur. To evaluate the importance of sex reversal among adult females, the blood of 78 animals was typed for the serologically detectable H-Y antigen, used as a tool to identify sexual genotype. In 73 of them, the H-Y phenotype was positive, conforming with female genotype, but in the other 5 females, it was negative (as in genotypic males), revealing that the sexual phenotype of these animals had been inverted. As the percentage of these sex-reversed genotypic males is low, the influence of temperature would appear not to be the sole cause of the observed unbalanced sex ratio. The female bias can be partly explained by the interaction of temperature with the ZZ/ZW system of genotypic sex determination. Indeed, in this system, sexual inversion under the influence of an epigenetic factor increases the ratio of genotypic females (ZW and WW) in the progeny.


2017 ◽  
Vol 372 (1729) ◽  
pp. 20160325 ◽  
Author(s):  
Veronika Bókony ◽  
Szilvia Kövér ◽  
Edina Nemesházi ◽  
András Liker ◽  
Tamás Székely

Sex reversals whereby individuals of one genetic sex develop the phenotype of the opposite sex occur in ectothermic vertebrates with genetic sex-determination systems that are sensitive to extreme temperatures during sexual differentiation. Recent rises in global temperatures have led researchers to predict that sex reversals will become more common, resulting in the distortion of many populations' sex ratios. However, it is unclear whether susceptibility to climate-driven sex-ratio shifts depends on the type of sex determination that varies across species. First, we show here using individual-based theoretical models that XX/XY (male-heterogametic) and ZZ/ZW (female-heterogametic) sex-determination systems can respond differentially to temperature-induced sex reversals. Interestingly, the impacts of climate warming on adult sex ratio (ASR) depend on the effects of both genotypic and phenotypic sex on survival and reproduction. Second, we analyse the temporal changes of ASR in natural amphibian populations using data from the literature, and find that ASR shifted towards males in ZZ/ZW species over the past 60 years, but did not change significantly in XX/XY species. Our results highlight the fact that we need a better understanding of the interactions between genetic and environmental sex-determining mechanisms to predict the responses of ectotherms to climate change and the associated extinction risks. This article is part of the themed issue ‘Adult sex ratios and reproductive decisions: a critical re-examination of sex differences in human and animal societies’.


2021 ◽  
Vol 112 (2) ◽  
pp. 155-164
Author(s):  
Suzanne Edmands

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 <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.


Genetics ◽  
1997 ◽  
Vol 147 (3) ◽  
pp. 1169-1180 ◽  
Author(s):  
Daven C Presgraves ◽  
Emily Severance ◽  
Gerald S Willrinson

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.


2000 ◽  
Vol 23 (1) ◽  
pp. 97-103 ◽  
Author(s):  
Lincoln S. Rocha ◽  
André Luiz P. Perondini

In sciarid flies, the control of sex determination and of the progeny sex ratio is exercised by the parental females, and is based on differential X-chromosome elimination in the initial stages of embryogenesis. In some species, the females produce unisexual progenies (monogenic females) while in others, the progenies consist of males and females (digenic females). The sex ratio of bisexual progenies is variable, and departs considerably from 1:1. Bradysia matogrossensis shows both monogenic and digenic reproduction. In a recently established laboratory strain of this species, 15% of the females were digenic, 10% produced only females, 13% produced only males, and 62% produced progenies with one predominant sex (33% predominantly of female and 29% predominantly male progenies). These progeny sex ratios were maintained in successive generations. Females from female-skewed progenies yielded female- and male-producing daughters in a 1:1 ratio. In contrast, daughters of females from male-skewed progenies produce bisexual or male-skewed progenies. The X-chromosome of B. matogrossensis shows no inversion or other gross aberration. These results suggest that the control of the progeny sex ratio (or differential X-chromosome elimination) involves more than one locus or, at least, more than one pair of alleles. The data also suggest that, in sciarid flies, monogeny and digeny may share a common control mechanism.


2010 ◽  
Vol 7 (2) ◽  
pp. 295-298 ◽  
Author(s):  
Sherman Silber ◽  
Jonathan H. Geisler ◽  
Minjin Bolortsetseg

It has been suggested that climate change at the Cretaceous–Palaeogene (K–Pg) boundary, initiated by a bolide impact or volcanic eruptions, caused species with temperature-dependent sex determination (TSD), including dinosaurs, to go extinct because of a skewed sex ratio towards all males. To test this hypothesis, the sex-determining mechanisms (SDMs) of Cretaceous tetrapods of the Hell Creek Formation (Montana, USA) were inferred using parsimony optimizations of SDMs on a tree, including Hell Creek species and their extant relatives. Although the SDMs of non-avian dinosaurs could not be inferred, we were able to determine the SDMs of 62 species; 46 had genotypic sex determination (GSD) and 16 had TSD. The TSD hypothesis for extinctions performed poorly, predicting between 32 and 34 per cent of survivals and extinctions. Most surprisingly, of the 16 species with TSD, 14 of them survived into the Early Palaeocene. In contrast, 61 per cent of species with GSD went extinct. Possible explanations include minimal climate change at the K–Pg, or if climate change did occur, TSD species that survived had egg-laying behaviour that prevented the skewing of sex ratios, or had a sex ratio skewed towards female rather than male preponderance. Application of molecular clocks may allow the SDMs of non-avian dinosaurs to be inferred, which would be an important test of the pattern discovered here.


2003 ◽  
Vol 81 (8) ◽  
pp. 1306-1311 ◽  
Author(s):  
Monica L Bond ◽  
Jerry O Wolff ◽  
Sven Krackow

We tested predictions associated with three widely used hypotheses for facultative sex-ratio adjustment of vertebrates using eight enclosed populations of gray-tailed voles, Microtus canicaudus. These were (i) the population sex ratio hypothesis, which predicts that recruitment sex ratios should oppose adult sex-ratio skews, (ii) the local resource competition hypothesis, which predicts female-biased recruitment at low adult population density and male-biased recruitment at high population density, and (iii) the first cohort advantage hypothesis, which predicts that recruitment sex ratios should be female biased in the spring and male biased in the autumn. We monitored naturally increasing population densities with approximately equal adult sex ratios through the spring and summer and manipulated adult sex ratios in the autumn and measured subsequent sex ratios of recruits. We did not observe any significant sex-ratio adjustment in response to adult sex ratio or high population density; we did detect an influence of time within the breeding season, with more female offspring observed in the spring and more male offspring observed in the autumn. Significant seasonal increases in recruitment sex ratios indicate the capacity of female gray-tailed voles to manipulate their offspring sex ratios and suggest seasonal variation in the relative reproductive value of male and female offspring to be a regular phenomenon.


Author(s):  
Shoshana Grossbard

This chapter reviews models of marriage, with special emphasis on how the sex ratio can help explain outcomes such as marriage formation, the intramarriage distribution of consumption goods, labor supply, savings, type of relationship, divorce, and intermarriage. Economic models of marriage pioneered by Gary Becker are reviewed in the first section and then extended in the next section to incorporate the labor market for the work-in-household approach of Grossbard. The following section discusses challenges in identifying exogenous variation in sex ratios and presents empirical evidence on the impact of sex ratios on labor supply, consumption, savings, and several other outcomes.


2013 ◽  
Vol 280 (1772) ◽  
pp. 20132460 ◽  
Author(s):  
Timothy S. Mitchell ◽  
Jessica A. Maciel ◽  
Fredric J. Janzen

Evolutionary theory predicts that dioecious species should produce a balanced primary sex ratio maintained by frequency-dependent selection. Organisms with environmental sex determination, however, are vulnerable to maladaptive sex ratios, because environmental conditions vary spatio-temporally. For reptiles with temperature-dependent sex determination, nest-site choice is a behavioural maternal effect that could respond to sex-ratio selection, as mothers could adjust offspring sex ratios by choosing nest sites that will have particular thermal properties. This theoretical prediction has generated decades of empirical research, yet convincing evidence that sex-ratio selection is influencing nesting behaviours remains absent. Here, we provide the first experimental evidence from nature that sex-ratio selection, rather than only viability selection, is probably an important component of nest-site choice in a reptile with temperature-dependent sex determination. We compare painted turtle ( Chrysemys picta ) neonates from maternally selected nest sites with those from randomly selected nest sites, observing no substantive difference in hatching success or survival, but finding a profound difference in offspring sex ratio in the direction expected based on historical records. Additionally, we leverage long-term data to reconstruct our sex ratio results had the experiment been repeated in multiple years. As predicted by theory, our results suggest that sex-ratio selection has shaped nesting behaviour in ways likely to enhance maternal fitness.


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