Male-biased sex ratios and plasticity in post-insemination behaviour in the New Zealand stick insect Micrarchus hystriculeus

Behaviour ◽  
2015 ◽  
Vol 152 (5) ◽  
pp. 653-666 ◽  
Author(s):  
Clint D. Kelly
Keyword(s):  
Sex Ratio ◽  
Sperm Competition ◽  
Laboratory Experiments ◽  
Sex Ratios ◽  
Mate Guarding ◽  
Stick Insect ◽  
Encounter Rate ◽  
Mate Fidelity ◽  
Biased Sex Ratio ◽  
Increasing Risk

The duration of mate guarding by males is predicted to vary in accordance with the risk of sperm competition or mate encounter rate. Mate guarding is predicted to be prolonged under a male-biased sex ratio because the risk of sperm competition is high or the mate encounter rate is low. A consistently male-biased sex ratio should thus select for greater mate fidelity, and reduced plasticity in guarding behaviour, by males. Micrarchus hystriculeus Westwood (Phasmatodea) is a sexually size dimorphic stick insect in which males form prolonged post-insemination associations with their mates and whose populations have a consistently male-biased sex ratio. My laboratory experiments showed, as predicted, little plasticity by males in the duration of their post-insemination association. Although mate guarding duration is similar under male- and female-biased sex ratios, males clasped the genitalia of their mates significantly more often under a male-biased sex ratio, suggesting that males intensify their guarding with increasing risk of sperm competition.

scholarly journals Fisher vs. The Worms: Extraordinary Sex Ratios in Nematodes and the Mechanisms That Produce Them

Cells ◽  
2021 ◽  
Vol 10 (7) ◽  
pp. 1793
Author(s):  
Justin Van Goor ◽  
Diane C. Shakes ◽  
Eric S. Haag
Keyword(s):  
Sex Ratio ◽  
Sperm Competition ◽  
Sex Chromosomes ◽  
Sex Ratios ◽  
Environmental Sex Determination ◽  
Fitness Advantage ◽  
Selection For ◽  
Facultative Parthenogenesis ◽  
Multicellular Organisms ◽  
Inbred Populations

Parker, Baker, and Smith provided the first robust theory explaining why anisogamy evolves in parallel in multicellular organisms. Anisogamy sets the stage for the emergence of separate sexes, and for another phenomenon with which Parker is associated: sperm competition. In outcrossing taxa with separate sexes, Fisher proposed that the sex ratio will tend towards unity in large, randomly mating populations due to a fitness advantage that accrues in individuals of the rarer sex. This creates a vast excess of sperm over that required to fertilize all available eggs, and intense competition as a result. However, small, inbred populations can experience selection for skewed sex ratios. This is widely appreciated in haplodiploid organisms, in which females can control the sex ratio behaviorally. In this review, we discuss recent research in nematodes that has characterized the mechanisms underlying highly skewed sex ratios in fully diploid systems. These include self-fertile hermaphroditism and the adaptive elimination of sperm competition factors, facultative parthenogenesis, non-Mendelian meiotic oddities involving the sex chromosomes, and environmental sex determination. By connecting sex ratio evolution and sperm biology in surprising ways, these phenomena link two “seminal” contributions of G. A. Parker. 

Male-biased sex ratio in Argulus canadensis Wilson, 1916 (Crustacea: Branchiura) ectoparasitic on sticklebacks

1989 ◽  
Vol 67 (8) ◽  
pp. 2078-2080 ◽  
Author(s):  
Robert Poulin ◽  
Gerard J. FitzGerald
Keyword(s):  
Salt Marsh ◽  
Sex Ratio ◽  
Laboratory Experiments ◽  
Fish Predation ◽  
Reproductive Behaviour ◽  
Egg Deposition ◽  
Alternative Hypotheses ◽  
Biased Sex Ratio ◽  
The Difference ◽  
Fish Hosts

Females of the ectoparasitic crustacean Argulus canadensis must leave their fish hosts at least temporarily to deposit their eggs on the substrate. To test the hypothesis that this difference in reproductive behaviour between the two sexes could result in male-biased sex ratios on their stickleback hosts, we sampled sticklebacks in tide pools of a Quebec salt marsh from early July to early September 1986. During this period, fish harboured significantly more male than female A. canadensis. Laboratory experiments were done to test two alternative hypotheses offered to explain this biased sex ratio. The first hypothesis was that male A. canadensis were more successful than females in attacking their stickleback hosts; however, we found no differences in attack success on their hosts between the two parasite sexes. The second hypothesis was that sticklebacks ate more female than male A. canadensis. Although males were less vulnerable to fish predation than females, the difference was not significant. We conclude that sexual differences in reproductive behaviour, i.e., egg deposition behaviour of females, can account for the male-biased sex ratio of A. canadensis on sticklebacks.

Effects of phytoseiid predators on the sex ratio of the spider mite Panonychus ulmi

1991 ◽  
Vol 69 (1) ◽  
pp. 208-212 ◽  
Author(s):  
Dan L. Johnson ◽  
Heather C. Proctor
Keyword(s):  
Population Density ◽  
Sex Ratio ◽  
Spider Mite ◽  
Total Population ◽  
Panonychus Ulmi ◽  
Encounter Rate ◽  
Male Mortality ◽  
Adult Sex Ratio ◽  
Biased Sex Ratio ◽  
Male Activity

The effect of predator presence on the adult sex ratio of a spider mite (Panonychus ulmi) was examined in a field experiment. Phytoseiid predators (chiefly Typhlodromus occidentalis) were removed from 32 trees harboring P. ulmi populations, and allowed to remain at natural levels on 32 other trees. Both total population density and proportion of males in the prey population were significantly higher in predator-free trees. Mechanisms that could explain the increase in the proportion of males are examined. The most probable is that greater male activity results in a higher encounter rate between predator and prey, and that subsequent higher male mortality when predators are present exaggerates the female-biased sex ratio. The theoretical effects of sex-biased predation on diplo-diploid and haplo-diploid organisms are discussed.

The effects of body size, ownership and sex-ratio on the precopulatory mate guarding of Caprella penantis (Crustacea: Amphipoda)

2009 ◽  
Vol 90 (2) ◽  
pp. 275-279 ◽  
Author(s):  
Fumio Takeshita ◽  
Yasuhisa Henmi
Keyword(s):  
Body Size ◽  
Sex Ratio ◽  
Laboratory Experiments ◽  
Mate Guarding ◽  
Operational Sex Ratio ◽  
Receptive Female ◽  
Type I ◽  
Male Body ◽  
Precopulatory Mate Guarding ◽  
Secondary Factor

Precopulatory mate guarding behaviour of the skeleton shrimp Caprella penantis is described. Moreover, the effects of body size, ownership and sex-ratio on mate guarding were examined experimentally in the laboratory. In the field population, the operational sex-ratio was male-biased. Guarding pairs, which were collected from the field, continued guarding for an average of 350 minutes in the laboratory, indicating that the normal guarding duration is approximately 10 hours. In this species, two guarding types were found: Type O and Type I-like. In Type O guarding, the male would fold the female into a horseshoe shape, whilst the male held the female parallel to him in Type I-like guarding. In the laboratory experiments, male body size was the most important factor affecting competition for a receptive female; ownership was the secondary factor. Guarding duration was prolonged when the sex-ratio was male-biased. Thus, the precopulatory mate guarding behaviour of C. penantis is influenced by several factors, such as body size, ownership and sex-ratio.

scholarly journals Evolution of male strategies with sex-ratio–dependent pay-offs: connecting pair bonds with grandmothering

2017 ◽  
Vol 372 (1729) ◽  
pp. 20170041 ◽  
Author(s):  
Sara L. Loo ◽  
Kristen Hawkes ◽  
Peter S. Kim
Keyword(s):  
Life History ◽  
Sex Ratio ◽  
Human Evolution ◽  
Paternal Care ◽  
Multiple Mating ◽  
Sex Ratios ◽  
Mate Guarding ◽  
Equation Model ◽  
Pair Bonding ◽  
Pair Bonds

Men's provisioning of mates and offspring has been central to ideas about human evolution because paternal provisioning is absent in our closest evolutionary cousins, the great apes, and is widely assumed to result in pair bonding, which distinguishes us from them. Yet mathematical modelling has shown that paternal care does not readily spread in populations where competition for multiple mates is the common male strategy. Here we add to models that point to the mating sex ratio as an explanation for pairing as pay-offs to mate guarding rise with a male-biased sex ratio. This is of interest for human evolution because our grandmothering life history shifts the mating sex ratio from female- to male-biased. Using a difference equation model, we explore the relative pay-offs for three competing male strategies (dependant care, multiple mating, mate guarding) in response to changing adult sex ratios. When fertile females are abundant, multiple mating prevails. As they become scarce, mate guarding triumphs. The threshold for this shift depends on guarding efficiency. Combined with mating sex ratios of hunter–gatherer and chimpanzee populations, these results strengthen the hypothesis that the evolution of our grandmothering life history propelled the shift to pair bonding in the human lineage. 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’.

Estimating sex ratios of loggerhead turtles in Brazil from pivotal incubation durations

1997 ◽  
Vol 75 (5) ◽  
pp. 755-770 ◽  
Author(s):  
Maria Ângela Marcovaldi ◽  
Matthew H. Godfrey ◽  
N. Mrosovsky
Keyword(s):  
Sex Ratio ◽  
Sexual Differentiation ◽  
Sex Ratios ◽  
Caretta Caretta ◽  
Temperature Dependent ◽  
Loggerhead Turtles ◽  
Biased Sex Ratio ◽  
Nesting Beaches

A method of estimating natural sex ratios of hatchlings of species with temperature-dependent sexual differentiation from data on incubation durations is described. The method was applied to loggerhead turtles (Caretta caretta) nesting in Brazil. Data on incubation durations were collected from 11 nesting beaches monitored for up to six seasons. It was estimated that 82.5% of the loggerhead hatchlings produced were female. The strongly female-biased sex ratio in Brazil is similar to that found previously for loggerheads using beaches in the eastern U.S.A. This suggests that a female-biased hatchling sex ratio may be a feature of loggerhead populations.

Mating Tactics in the Tropical Millipede Alloporus Uncinatus (Diplopoda: Spirostreptidae)

Behaviour ◽  
1993 ◽  
Vol 124 (1-2) ◽  
pp. 45-56 ◽  
Author(s):  
Steven R. Telford ◽  
J. Mark Dangerfield
Keyword(s):  
Sex Ratio ◽  
Mating System ◽  
Sperm Competition ◽  
Breeding Season ◽  
Female Choice ◽  
Laboratory Experiments ◽  
Mating Behaviour ◽  
Operational Sex Ratio ◽  
Mating Tactics ◽  
Mate Acquisition

AbstractField and laboratory observations of mating behaviour in a population of the tropical millipede Alloporus uncinatus were carried out over one breeding season. Males obtained mates through random encounters and by forming triplet associations with copula pairs. The occurrence of triplet associations in the field was coincident with a highly male biased operational sex ratio. Mate acquisition by males was apparently stochastic and direct physical competition did not occur. In laboratory experiments mating was size-selective probably as a consequence of female choice. We consider the possibility that sperm competition has contributed to the evolution of the mating system in this species.

scholarly journals Solving the sex ratio scandal in Melittobia wasps

2020 ◽  
Author(s):  
Jun Abe ◽  
Ryosuke Iritani ◽  
Koji Tsuchida ◽  
Yoshitaka Kamimura ◽  
Stuart A. West
Keyword(s):  
Sex Ratio ◽  
Sex Allocation ◽  
Laboratory Experiments ◽  
Sex Ratios ◽  
Local Mate Competition ◽  
Mate Competition ◽  
Offspring Sex ◽  
Local Mate ◽  
Close Relatives

AbstractThe scandalous sex ratio behaviour of Melittobia wasps has long posed one of the greatest problems for the field of sex allocation. In contrast to the predictions of theory, and the behaviour of numerous other organisms, laboratory experiments have found that Melittobia females do not produce less female-biased offspring sex ratios when more females lay eggs on a patch. We resolve this scandal, by showing that, in nature, females of M. australica have sophisticated sex ratio behaviour, where their strategy also depends upon whether they have dispersed from the patch where they emerged. When females have not dispersed, they will be laying eggs with close relatives, which keeps local mate competition high, even with multiple females, and so they are selected to produce consistently female-biased sex ratios. Laboratory experiments mimic these conditions. In contrast, when females disperse, they will be interacting with non-relatives, and so they adjust their sex ratio depending upon the number of females laying eggs. Consequently, females appear to use dispersal status as an indirect cue of relatedness, and whether they should adjust their sex ratio in response to the number of females laying eggs on the patch.

scholarly journals Cooperative interactions among females and even more extraordinary sex ratios

2020 ◽  
Author(s):  
Ryosuke Iritani ◽  
Stuart A West ◽  
Jun Abe
Keyword(s):  
Sex Ratio ◽  
Sex Ratios ◽  
Structured Populations ◽  
Local Mate Competition ◽  
Mate Competition ◽  
Wasp Species ◽  
Cooperative Interactions ◽  
Competition Theory ◽  
Local Mate ◽  
Biased Sex Ratio

AbstractHamilton’s local mate competition theory provided an explanation for extraordinary female biased sex ratios in a range of organisms. When mating takes place locally, in structured populations, a female biased sex ratio is favoured to reduce competition between related males, and to provide more mates for males. However, there are a number of wasp species where the sex ratios appear to more female biased than predicted by Hamilton’s theory. We investigated theoretically the extent to which cooperative interactions between related females can interact with local mate competition to favour even more female biased sex ratios. We found that: (i) cooperative interactions between females can lead to sex ratios that are more female biased than predicted by local competition theory alone; (ii) sex ratios can be more female biased when the cooperative interactions are offspring helping parents before dispersal, rather than cooperation between siblings after dispersal. Our results can be applied to a range of organisms, and provide an explanation for the extreme sex ratio biases that have been observed in Sclerodermus and Melittobia wasps.

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.

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