scholarly journals Effects of Selection on the Evolution of the Sex Ratio

1982 ◽  
Vol 35 (1) ◽  
pp. 95 ◽  
Author(s):  
DJ Colgan
Keyword(s):  
Sex Ratio ◽  
Sex Determination ◽  
Parental Investment ◽  
Sex Ratios ◽  
Natural Populations ◽  
Viability Selection

Hypotheses as to the biological bases of observed sex ratios must explain the departures found in natural populations from the ratio which might be expected from the mechanism of sex determination in the species. Models based on the concept of parental investment (Fisher 1930) have been used to explain such departures but do not predict equilibrium sex ratios when viability selection discriminates between the sexes in the period between the end of parental investment and the maturity of the offspring.

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 <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.

scholarly journals Analysis of the sex ratio in Bradysia matogrossensis (Diptera, Sciaridae)

2000 ◽  
Vol 23 (1) ◽  
pp. 97-103 ◽  
Author(s):  
Lincoln S. Rocha ◽  
André Luiz P. Perondini
Keyword(s):  
Sex Ratio ◽  
Sex Determination ◽  
X Chromosome ◽  
Control Mechanism ◽  
Sex Ratios ◽  
Laboratory Strain ◽  
Chromosome Elimination ◽  
Common Control ◽  
Males And Females ◽  
Successive Generations

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.

scholarly journals Does sex-ratio selection influence nest-site choice in a reptile with temperature-dependent sex determination?

2013 ◽  
Vol 280 (1772) ◽  
pp. 20132460 ◽  
Author(s):  
Timothy S. Mitchell ◽  
Jessica A. Maciel ◽  
Fredric J. Janzen
Keyword(s):  
Sex Ratio ◽  
Sex Determination ◽  
Nest Site ◽  
Sex Ratios ◽  
Temperature Dependent ◽  
Dioecious Species ◽  
Offspring Sex Ratio ◽  
Nest Sites ◽  
Offspring Sex ◽  
Nest Site Choice

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.

Sex ratios and survival in fluctuating populations of the deer mouse, Peromyscus mamculatus borealis

1970 ◽  
Vol 48 (4) ◽  
pp. 809-811 ◽  
Author(s):  
Raymond P. Canham
Keyword(s):  
Population Density ◽  
Sex Ratio ◽  
Deer Mouse ◽  
Sex Ratios ◽  
Natural Populations ◽  
In Captivity ◽  
Males And Females ◽  
Young Of The Year ◽  
Fluctuating Populations ◽  
Number Of Males

In litters of the deer mouse, Peromyscus mamculatus borealis, born in captivity there was a significantly greater number of males than females. In natural populations of the same subspecies, an excess of males caused the sex ratio in captured young of the year to differ significantly from 1:1 only in those summers in which population density increased considerably. The sex ratio did not change appreciably during a winter in which density remained stable, but in winters of low survival the proportion of males declined. A difference between males and females in the amplitude of the fluctuations in postnatal survival thus appeared responsible for variations in the sex ratio.

scholarly journals Demographic and genetic consequences of disturbed sex determination

2017 ◽  
Vol 372 (1729) ◽  
pp. 20160326 ◽  
Author(s):  
Claus Wedekind
Keyword(s):  
Population Growth ◽  
Sex Determination ◽  
Sex Ratios ◽  
Natural Populations ◽  
Gonad Development ◽  
Empirical Work ◽  
Sex Reversal ◽  
Negative Effects ◽  
Population Extinction

During sex determination, genetic and/or environmental factors determine the cascade of processes of gonad development. Many organisms, therefore, have a developmental window in which their sex determination can be sensitive to, for example, unusual temperatures or chemical pollutants. Disturbed environments can distort population sex ratios and may even cause sex reversal in species with genetic sex determination. The resulting genotype–phenotype mismatches can have long-lasting effects on population demography and genetics. I review the theoretical and empirical work in this context and explore in a simple population model the role of the fitness v yy of chromosomally aberrant YY genotypes that are a consequence of environmentally induced feminization. Low v yy is mostly beneficial for population growth. During feminization, low v yy reduces the proportion of genetic males and hence accelerates population growth, especially at low rates of feminization and at high fitness costs of the feminization itself (i.e. when feminization would otherwise not affect population dynamics much). When sex reversal ceases, low v yy mitigates the negative effects of feminization and can even prevent population extinction. Little is known about v yy in natural populations. The available models now need to be parametrized in order to better predict the long-term consequences of disturbed sex determination. 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’.

Effects of hatchery shading and nest depth on the development and quality of Chelonia mydas hatchlings: implications for hatchery management in Peninsular, Malaysia

2005 ◽  
Vol 53 (3) ◽  
pp. 205 ◽  
Author(s):  
Jason van de Merwe ◽  
Kamarruddin Ibrahim ◽  
Joan Whittier
Keyword(s):  
Sex Ratio ◽  
Sex Ratios ◽  
Natural Populations ◽  
Chelonia Mydas ◽  
Condition Index ◽  
Peninsular Malaysia ◽  
Sex Characteristics ◽  
Poor Correlation ◽  
Emergence Success ◽  
Nest Depth

One of the decisions made by hatchery managers around the world is what degree of shading and nest depth are required to maximise the production of high-quality hatchlings at optimal sex ratios. The primary objectives of this study were to determine the effects of (1) hatchery shading and nest depth on nest temperatures and emergence lag, and (2) nest temperatures and nest depth on hatchling sex ratio and quality. In 2001, 26 Chelonia mydas clutches from Ma’Daerah beach, Terengganu, Malaysia, were relocated alternatively at depths of 50 cm and 75 cm into a 70%-shaded and a 100%-shaded hatchery. Data loggers were placed into the centre of each relocated clutch to record the temperature every hour over the course of incubation. When the hatchlings emerged, a sample of the clutch was run, measured and weighed and a separate sample was examined histologically for sex characteristics. Nest temperatures ranged between 28°C and 30°C and generally showed increases over the second half of incubation due to metabolic heating of the clutch. There was no significant correlation found between nest temperature and any of the hatchling parameters measured. Hatchlings from 75-cm-deep nests had a longer emergence lag (46.4 (±10.2) h) than hatchlings from 50-cm-deep nests. Hatch and emergence success were similar to those of natural populations and hatchling sex ratios were male dominant, with an average of 72% males. There was a poor correlation between mean middle-third incubation temperatures and sex ratio. Hatchlings from 75-cm-deep nests had similar running speeds but lower condition index than their conspecifics from 50-cm-deep nests.

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.

The genetic basis of sex ratio in Silene alba (= S. latifolia).

Genetics ◽  
1994 ◽  
Vol 136 (2) ◽  
pp. 641-651
Author(s):  
D R Taylor
Keyword(s):  
Sex Ratio ◽  
Sex Ratios ◽  
Natural Populations ◽  
Sex Ratio Bias ◽  
Deleterious Alleles ◽  
Silene Alba ◽  
Biased Sex Ratio ◽  
Paternal Parent ◽  
Reciprocal Crossing ◽  
Female Bias

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.

scholarly journals Relative frequencies of the “sex-ratio” inversion in natural populations of Drosophila pseudoobscura from Mexico

Genetika ◽  
2011 ◽  
Vol 43 (2) ◽  
pp. 321-329 ◽  
Author(s):  
Víctor Salceda
Keyword(s):  
Sex Ratio ◽  
Sex Determination ◽  
Salivary Glands ◽  
Sex Chromosome ◽  
Natural Populations ◽  
Drosophila Pseudoobscura ◽  
X Chromosomes ◽  
The Third ◽  
Single Larva ◽  
East West

Sex-ratio (proportion of males) in a species is related to a not entirely explained mechanism of sex determination. In Drosophila, sex is determined by the proportion of X chromosomes vs. autosomes. A decrease in the proportion of males vs. females, known as sex-ratio, is characteristic to several Drosophila species, and is related to an inversion in the sexual chromosome the so called ?sex-ratio? (SR) condition. In this occasion we study the presence of that inversion in several populations of Drosophila pseudoobscura from Mexico. With this purpose we did collections of this species on Nevado de Colima,Col., Valpara?so, Zac, Zirahu?n, Mich., Tulancingo, Hgo. and Amecameca, Mex. Flies were captured in nature and carried to the laboratory were individual cultures of each female were established, when the offsprig emerged salivary glands of a single larva from each culture were extracted and stained with an aceto-orcein solution and the corresponding genotype for the third and sex chromosome determined and their relative frequencies calculated. The corresponding frequencies of the ?sex-ratio? inversion in the localities analyzed were: Nevado de Colima 21.8 %, Valparaiso 18.8 %, Zirahu?n 11.4 %, Tulancingo 6.8 % and Amecameca 6.8 %. Apparently an East-West cline distribution is present in these populations. Relative frequencies for inversions in the third chomosome were recorded and relationships between third and X chromosomes inversions performed. Comparisons with similar studies on this and other species are pointed out.

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