scholarly journals Seed sexing revealed female bias in two Rumex species

2011 ◽  
Vol 80 (2) ◽  
pp. 93-97 ◽  
Author(s):  
Dagmara Kwolek ◽  
Andrzej J. Joachimiak
Keyword(s):  
Sex Ratio ◽  
Sex Chromosomes ◽  
Dna Markers ◽  
Sex Chromosome ◽  
Sex Ratios ◽  
Ratio Bias ◽  
Sex Ratio Bias ◽  
Y Chromosomes ◽  
Sex Chromosome System ◽  
Female Bias

Sex-ratio bias in seeds of dioecious <em>Rumex</em> species with sex chromosomes is an interesting and still unsettled issue. To resolve gender among seeds of <em>R. acetosa</em> and <em>R. thyrsiflorus</em> (two species with an XX/XY1Y2 sex chromosome system), this work applied a PCR-based method involving DNA markers located on Y chromosomes. Both species showed female-biased primary sex ratios, with female bias greater in <em>R. acetosa</em> than in <em>R. thyrsiflorus</em>. The observed predominance of female seeds is consistent with the view that the female biased sex ratios in <em>Rumex </em>are conditioned not only postzygotically but also prezygotically.

scholarly journals A father effect explains sex-ratio bias

2017 ◽  
Vol 284 (1861) ◽  
pp. 20171159 ◽  
Author(s):  
Aurelio F. Malo ◽  
Felipe Martinez-Pastor ◽  
Francisco Garcia-Gonzalez ◽  
Julián Garde ◽  
Jonathan D. Ballou ◽  
...  
Keyword(s):  
Genetic Variation ◽  
Sex Ratio ◽  
Sex Chromosome ◽  
Sex Ratios ◽  
Sperm Nucleus ◽  
Equal Proportion ◽  
Offspring Sex Ratio ◽  
Ratio Bias ◽  
Sex Ratio Bias ◽  
Offspring Sex

Sex ratio allocation has important fitness consequences, and theory predicts that parents should adjust offspring sex ratio in cases where the fitness returns of producing male and female offspring vary. The ability of fathers to bias offspring sex ratios has traditionally been dismissed given the expectation of an equal proportion of X- and Y-chromosome-bearing sperm (CBS) in ejaculates due to segregation of sex chromosomes at meiosis. This expectation has been recently refuted. Here we used Peromyscus leucopus to demonstrate that sex ratio is explained by an exclusive effect of the father, and suggest a likely mechanism by which male-driven sex-ratio bias is attained. We identified a male sperm morphological marker that is associated with the mechanism leading to sex ratio bias; differences among males in the sperm nucleus area (a proxy for the sex chromosome that the sperm contains) explain 22% variation in litter sex ratio. We further show the role played by the sperm nucleus area as a mediator in the relationship between individual genetic variation and sex-ratio bias. Fathers with high levels of genetic variation had ejaculates with a higher proportion of sperm with small nuclei area. This, in turn, led to siring a higher proportion of sons (25% increase in sons per 0.1 decrease in the inbreeding coefficient). Our results reveal a plausible mechanism underlying unexplored male-driven sex-ratio biases. We also discuss why this pattern of paternal bias can be adaptive. This research puts to rest the idea that father contribution to sex ratio variation should be disregarded in vertebrates, and will stimulate research on evolutionary constraints to sex ratios—for example, whether fathers and mothers have divergent, coinciding, or neutral sex allocation interests. Finally, these results offer a potential explanation for those intriguing cases in which there are sex ratio biases, such as in humans.

Estimating the Frequency of Constrained Sex Allocation in Field Populations of Hymenoptera

Behaviour ◽  
1990 ◽  
Vol 114 (1-4) ◽  
pp. 137-147 ◽  
Author(s):  
H.C.J. Godfray ◽  
I.C.W. Hardy
Keyword(s):  
Sex Ratio ◽  
Sex Allocation ◽  
Sex Ratios ◽  
Parasitoid Species ◽  
Ratio Bias ◽  
Sex Ratio Bias ◽  
Sex Ratio Theory

Abstract1) Sex ratio theory has assumed that females can produce offspring of both sexes. It has been suggested that some females in haplodiploid populations are only able to produce sons (constrained sex allocation), for example because they are virgin. The presence of such females influences the optimal sex ratio of unconstrained females. The relevance of these ideas to field sex ratios is largely untested. 2) The frequencies of constrained oviposition in three Drosophila parasitoid species are estimated. Constrained, ovipositing females were distinguished by the absence of sperm in the spermatheca. Constrained females were absent or rare in these species. 3) We review data from the literature that allow an estimate of the frequency of constrained females. 4) We conclude that the available evidence suggests that while constrained oviposition is uncommon, there are some species in which constrained females are sufficiently common to select for an observable sex ratio bias by unconstrained females.

scholarly journals Sex chromosomes, sex ratios and sex gaps in longevity in plants

2021 ◽  
Author(s):  
Gabriel AB Marais ◽  
Jean-Francois Lemaitre
Keyword(s):  
Sex Chromosomes ◽  
Statistical Power ◽  
Sex Chromosome ◽  
Sex Ratios ◽  
Y Chromosomes ◽  
Adult Sex Ratio ◽  
Female Longevity ◽  
Males And Females ◽  
The Relationship

In animals, males and females can display markedly different longevity (also called sex gap in longevity, SGLs). Recent work has revealed that sex chromosomes contribute to establishing these SGLs. X-hemizygosity and toxicity of the Y chromosomes are two mechanisms that have been suggested to reduce male longevity (Z-hemizygosity and W toxicity in females in ZW systems). In plants, SGLs are known to exist but the role of sex chromosomes remains to be established. Here, by using adult sex ratio as a proxy for measuring SGLs, we explored the relationship between sex chromosome and SGLs across 43 plant species. Based on the knowledge recently accumulated in animals, we specifically asked whether: (i) species with XY systems tend to have female-biased sex ratios (reduced male longevity) and species with ZW ones tend to have male-biased sex ratios (reduced female longevity), and (ii) this patterns was stronger in heteromorphic systems compared to homomorphic ones. Our results tend to support these predictions although we lack statistical power because of a small number of ZW systems and the absence of any heteromorphic ZW system in the dataset. We discuss the implications of these findings, which we hope will stimulate further research on sex-differences in lifespan and ageing across plants.

A cytological study of species in Cnephia s. str. (Diptera: Simuliidae)

1982 ◽  
Vol 60 (11) ◽  
pp. 2866-2878 ◽  
Author(s):  
William S. Procunier
Keyword(s):  
Sex Chromosomes ◽  
Sex Chromosome ◽  
Cytological Study ◽  
Chromosome Complement ◽  
Nucleolar Organizer ◽  
Sympatric Speciation ◽  
Basic Chromosome ◽  
Y Chromosomes ◽  
Norwegian Population ◽  
Sex Chromosome System

Cytological descriptions and phylogenetic relationships are presented for the genus Cnephia s. str. All members are male achiasmate. Cnephia lapponica is unique in that its basic chromosome complement is reduced from n = 3 to n = 2 metacentrics as a result of a fusion of chromosomes II and III. Sex chromosome differentiation varies from nonobservable in C. ornithophilia and C. eremites through C. pecuarum in which the standard and IS-5 sequences are distributed differentially over X and Y chromosomes, to the polytypic system of C. lapponica in which the X chromosome is fixed for expression of the nucleolar organizer (NO) and the Y chromosome for nonexpression. Further, in a Norwegian population of C. lapponica, males are additionally interchange heterozygotes. Thus, a multiple sex chromosome system exists in which all the chromosomes are sex chromosomes. Closest members occur sympatrically and differ by sex chromosomes and at least one fixed inversion; more distant taxa differ by a number of fixed inversions as well as sex chromosomes. The identical bands 17B and 24C, which appear in a thin or enhanced form, are polymorphic, sex-linked, fixed, or lost in different members of the group. This study supports a model for sympatric speciation.

scholarly journals Causes of sex ratio bias may account for unisexual sterility in hybrids: a new explanation of Haldane's rule and related phenomena.

Genetics ◽  
1991 ◽  
Vol 128 (4) ◽  
pp. 841-858 ◽  
Author(s):  
L D Hurst ◽  
A Pomiankowski
Keyword(s):  
Sex Ratio ◽  
Sex Chromosome ◽  
Meiotic Drive ◽  
Maternal Transmission ◽  
Haldane’S Rule ◽  
Haldane's Rule ◽  
Sex Ratio Bias ◽  
Y Chromosomes ◽  
Heterogametic Sex ◽  
Hybrid Cross

Abstract Unisexual hybrid disruption can be accounted for by interactions between sex ratio distorters which have diverged in the species of the hybrid cross. One class of unisexual hybrid disruption is described by Haldane's rule, namely that the sex which is absent, inviable or sterile is the heterogametic sex. This effect is mainly due to incompatibility between X and Y chromosomes. We propose that this incompatibility is due to a mutual imbalance between meiotic drive genes, which are more likely to evolve on sex chromosomes than autosomes. The incidences of taxa with sex chromosome drive closely matches those where Haldane's rule applies: Aves, Mammalia, Lepidoptera and Diptera. We predict that Haldane's rule is not universal but is correct for taxa with sex chromosome meiotic drive. A second class of hybrid disruption affects the male of the species regardless of which sex is heterogametic. Typically the genes responsible for this form of disruption are cytoplasmic. These instances are accounted for by the release from suppression of cytoplasmic sex ratio distorters when in a novel nuclear cytotype. Due to the exclusively maternal transmission of cytoplasm, cytoplasmic sex ratio distorters cause only female-biased sex ratios. This asymmetry explains why hybrid disruption is limited to the male.

Analysis of SINE and LINE repeat content of Y chromosomes in the platypus, Ornithorhynchus anatinus

2009 ◽  
Vol 21 (8) ◽  
pp. 964 ◽  
Author(s):  
R. Daniel Kortschak ◽  
Enkhjargal Tsend-Ayush ◽  
Frank Grützner
Keyword(s):  
Sex Chromosomes ◽  
Sex Chromosome ◽  
Activity Patterns ◽  
Specific Sequence ◽  
X Chromosomes ◽  
Repeat Content ◽  
Y Chromosomes ◽  
Ornithorhynchus Anatinus ◽  
History Of ◽  
Sex Chromosome System

Monotremes feature an extraordinary sex-chromosome system that consists of five X and five Y chromosomes in males. These sex chromosomes share homology with bird sex chromosomes but no homology with the therian X. The genome of a female platypus was recently completed, providing unique insights into sequence and gene content of autosomes and X chromosomes, but no Y-specific sequence has so far been analysed. Here we report the isolation, sequencing and analysis of ~700 kb of sequence of the non-recombining regions of Y2, Y3 and Y5, which revealed differences in base composition and repeat content between autosomes and sex chromosomes, and within the sex chromosomes themselves. This provides the first insights into repeat content of Y chromosomes in platypus, which overall show similar patterns of repeat composition to Y chromosomes in other species. Interestingly, we also observed differences between the various Y chromosomes, and in combination with timing and activity patterns we provide an approach that can be used to examine the evolutionary history of the platypus sex-chromosome chain.

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 Sexual dimorphism and sex ratio bias in the dioecious willow Salix purpurea L

2020 ◽  
Author(s):  
Fred E. Gouker ◽  
Craig H. Carlson ◽  
Junzhu Zou ◽  
Luke Evans ◽  
Chase R. Crowell ◽  
...  
Keyword(s):  
Sexual Dimorphism ◽  
Sex Ratio ◽  
Sex Ratios ◽  
Field Trials ◽  
Nitrogen Accumulation ◽  
Dioecious Species ◽  
Ratio Bias ◽  
Diversity Panel ◽  
Sex Ratio Bias ◽  
Salix Purpurea

AbstractPremiseSexual dimorphism in dioecious plant species is often not obvious or is absent. Dioecious species populations also often exhibit deviations from expected sex ratios. Previous studies on members of the Salicaceae family have shown strong, partial, and no sexual dimorphism. Some studies have shown sex-biased ratios in several Salix spp., however, S. purpurea has never been examined for evidence of sexual dimorphism or for the presence of sex-ratio bias, and therefore a comprehensive phenotypic study is needed to fill this knowledge gap.MethodsThis study examined a suite of morphological, phenological, physiological and wood composition traits from multi-environment and multi-year replicated field trials in a diversity panel of unrelated S. purpurea accessions and in full-sib F1 and F2 families produced through controlled cross pollinations to test for sexual dimorphism and sex ratio bias.Key ResultsSignificant evidence of sexual dimorphism was found in vegetative traits with greater means for many traits in male genotypes compared to females across three populations of S. purpurea, measured across multiple years that were highly predictive of biomass yield. Male plants exhibited greater nitrogen accumulation under fertilizer amendment as measured by SPAD in the diversity panel, and males showed greater susceptibility to fungal infection by Melampsora spp in the F2 family. There were also consistent female-biased sex ratios in both the F1 and F2 families.ConclusionsThese results provide the first evidence of sexual dimorphism in S. purpurea and also confirm the prevalence of female-biased sex ratios previously found in other Salix species.

scholarly journals Haploid selection, sex ratio bias, and transitions between sex-determining systems

2018 ◽  
Author(s):  
Michael Francis Scott ◽  
Matthew Miles Osmond ◽  
Sarah Perin Otto
Keyword(s):  
Sex Ratio ◽  
Sex Determination ◽  
Sex Chromosomes ◽  
Pollen Competition ◽  
Diploid Males ◽  
Mendelian Segregation ◽  
Male And Female ◽  
Ratio Bias ◽  
Sex Ratio Bias ◽  
Haploid Selection

AbstractSex determination is remarkably dynamic; many taxa display shifts in the location of sex-determining loci or the evolution of entirely new sex-determining systems. Predominant theories for why we observe such transitions generally conclude that novel sex-determining systems are favoured by selection if they equalise the sex ratio or increase linkage with a locus that experiences different selection in males vs. females. We use population genetic models to extend these theories in two ways: (1) We consider the dynamics of loci very tightly linked to the ancestral sex-determining loci, e.g., within the non-recombining region of the ancestral sex chromosomes. Variation at such loci can favour the spread of new sex-determining systems in which the heterogametic sex changes (XY to ZW or ZW to XY) and the new sex-determining region is less closely linked (or even unlinked) to the locus under selection. (2) We consider selection upon haploid genotypes either during gametic competition (e.g., pollen competition) or meiosis (i.e., non-Mendelian segregation), which can cause the zygotic sex ratio to become biased. Haploid selection can drive transitions between sex-determining systems without requiring selection to act differently in diploid males vs. females. With haploid selection, we find that transitions between male and female heterogamety can evolve where linkage with the sex-determining locus is either strengthened or weakened. Furthermore, we find that sex-ratio biases may increase or decrease with the spread of new sex chromosomes, which implies that transitions between sex-determining systems cannot be simply predicted by selection to equalise the sex ratio. In fact, under many conditions, we find that transitions in sex determination are favoured equally strongly in cases where the sex ratio bias increases or decreases. Overall, our models predict that sex determination systems should be highly dynamic, particularly when haploid selection is present, consistent with the evolutionary lability of this trait in many taxa.Author summarySystems of sex determination are strikingly diverse and labile in many clades. This poses the question: what drives transitions between sex-determining systems? Here, we use models to derive conditions under which new sex-determining systems spread. Prevailing views suggest that new sex-determining systems are favoured when they equalize the sex ratio and/or when they are more closely linked to genes that experience differential selection in males and females. Our models include selection upon haploid genotypes (meiotic drive or gametic competition), which biases the sex-ratio and occurs differently in male and female gametes. Surprisingly, we find the two forces (selection to equalize the sex ratio and the benefits of hitchhiking alongside driven alleles that distort the sex ratio) will often be equally strong, and thus neither is sufficient to explain the spread of new sex-determining systems in every case. We also find that new sex-determining alleles can spread despite being less closely linked to selected loci as long as initial linkage is tight or haploid selection is present. Our models therefore predict that loci in previously unexpected genomic locations and/or experiencing various types of selection (including haploid selection) can now be implicated as drivers of transitions between sex-determining systems.

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