scholarly journals Nestling Sex Ratios in the Yellow-Naped Amazon: No Evidence for Adaptive Modification

The Condor ◽  
2002 ◽  
Vol 104 (2) ◽  
pp. 437-440 ◽  
Author(s):  
Jason M. South ◽  
Timothy F. Wright

AbstractMany birds, including some parrots, may adjust the sex ratio of their offspring in relation to the relative fitness benefits of sons and daughters. We investigated nestling sex ratios in Yellow-naped Amazons (Amazona auropalliata) using a molecular sexing technique that amplifies intronic regions of the CHD-W and CHD-Z genes in birds. We examined all nestlings in 37 complete clutches comprising 77 chicks. The overall nestling sex ratio did not differ from unity. Sex allocation was not associated with hatch date, sequence of hatching, or clutch size. We also found no difference in sex ratio between two regional dialects. Female Yellow-naped Amazons may be unable to control their hatchling sex ratio. Alternatively, there may be no fitness benefits to females producing more of one sex in relation to the factors we measured here.No Existe Evidencia que Indique Modificaciones Adaptativas de la Proporción de Sexos en la Progenie de Amazona auropalliataResumen. En muchas aves, incluyendo los loros, la proporción de sexos en la progenie puede ajustarse en relación a los beneficios relativos de adecuación biológica de hembras y machos. Dichas tasas fueron investigadas en Amazona auropalliata por medio de una técnica molecular de determinación sexual por la cual se amplifican regiones intrónicas de los genes CHD-W y CHD-Z de aves. Se examinaron todos los pichones de 37 nidadas completas, constituidas por 77 pichones. La proporción de sexos total no resultó diferente a uno. La asignación sexual no estuvo correlacionada con la fecha de eclosión, la secuencia de eclosión, ni el tamaño de la nidada. Tampoco se encontraron diferencias en las proporciones de sexos entre dos dialectos vocales regionales. Las hembras de A. auropalliata podrían no tener la habilidad de controlar la proporción de sexos de su progenie. Alternativamente, es posible que en términos de adecuación biológica, no haya diferencia en el beneficio de producir una progenie enriquecida en un sexo determinado con respecto a los factores medidos en este estudio.

2021 ◽  
Author(s):  
◽  
Elizabeth Victoria Berkeley

<p>The application of sex allocation theory can provide useful insight into endangered rhinoceros biology to improve in situ and ex situ conservation efforts by understanding the factors that cause a female to produce one sex of calf. By decreasing the birth sex ratio (number of males born per number of females born) in a population it may be possible to increase population growth rates. The first aim was to determine if an environmentally cued sex allocation response occurred in black rhinos. By examining rainfall and calf sex records in a wild black rhino population, I identified that birth sex ratios increase in rainy seasons and rainy years. Mothers were more likely to be observed with male calves if they conceived during the wet season (57.3% male) than during the dry season (42.9% male). Mothers were more likely to raise male calves if they conceived during wet years (60.2% male) than during dry years (46.1% male). Next, I examined whether pulsatile or random variation in sex ratios of different magnitudes, as might occur under changes in climate patterns, would be detrimental to rhinoceros population growth. Results demonstrated that while random increases in the magnitude of birth sex ratio variation, in either direction, increased population survival probability up to 0.907, sequential pulsed years of birth sex ratio bias had the opposite effect on population performance down to a survival probability of 0.619. Furthermore, for both scenarios, populations of less than 50 animals are particularly vulnerable to extinction. Since the sex biases observed in the captive rhinoceros population were attributed to several factors, I used an information theoretic approach to evaluate the relative importance of different hypotheses for birth sex bias for predicting calf sex. The results demonstrated that none of the models tested were greatly predictive of calf sex. Suspecting that the mechanisms that were cueing calf sex occur close to the time of conception and were nutritionally cued, in the final experiment, I measured changes in blood glucose in white rhinos after they ate different meals. At 90 minutes, serum glucose levels in rhinos eating the 10 % lucerne hay diet were significantly lower than the 5% glucose and 10% glucose diets but not the 10% pellet nor 10% grass hay diets. This is the first time such an experiment has been published in a wildlife species and not only demonstrates the feasibility of training rhinos for successive blood draws but also that captive diets are low glycemic for white rhinos. Overall, my research confirmed that an environmentally cued sex allocation response does occur in African rhinos, and changes in the duration and magnitude of sex ratio patterns can decrease population growth and increase potential for extinction. Additionally, none of the previous hypotheses for the suspected male-sex bias in captive born rhinos were influential on calf sex, which shifts the focus of sex allocation research in rhinos to more acute signals around the time of conception, such as changes in diet and body condition.</p>


2020 ◽  
Vol 16 (6) ◽  
pp. 20190929
Author(s):  
Renée C. Firman ◽  
Jamie N. Tedeschi ◽  
Francisco Garcia-Gonzalez

Mammal sex allocation research has focused almost exclusively on maternal traits, but it is now apparent that fathers can also influence offspring sex ratios. Parents that produce female offspring under conditions of intense male–male competition can benefit with greater assurance of maximized grand-parentage. Adaptive adjustment in the sperm sex ratio, for example with an increase in the production of X-chromosome bearing sperm (CBS), is one potential paternal mechanism for achieving female-biased sex ratios. Here, we tested this mechanistic hypothesis by varying the risk of male–male competition that male house mice perceived during development, and quantifying sperm sex ratios at sexual maturity. Our analyses revealed that males exposed to a competitive ‘risk’ produced lower proportions of Y-CBS compared to males that matured under ‘no risk’ of competition. We also explored whether testosterone production was linked to sperm sex ratio variation, but found no evidence to support this. We discuss our findings in relation to the adaptive value of sperm sex ratio adjustments and the role of steroid hormones in socially induced sex allocation.


1998 ◽  
Vol 88 (1) ◽  
pp. 37-45 ◽  
Author(s):  
K.M. Heinz

AbstractAn often encountered problem associated with augmentative and inundative biological control programmes is the high cost of producing sufficient numbers of natural enemies necessary to suppress pest populations within the time constraints imposed by ephemeral agroecosystems. In many arrhenotokous parasitoids, overproduction of males in mass-rearing cultures inflates costs (per female) and thus limits the economic feasibility of these biological control programmes. Within the context of existing production technologies, experiments were conducted to determine if the sex ratio ofCatolaccus grandis(Burks), an ectoparasitoid of the boll weevilAnthonomous grandisBoheman, varied as a function of boll weevil larval size. Results from natural and manipulative experiments demonstrate the following behavioural characteristics associated with C.grandissex allocation behaviour: (i) femaleC. grandisoffspring are produced on large size hosts and male offspring are produced on small hosts; (ii) whether a host is considered large or small depends upon the overall distribution of host sizes encountered by a female parasitoid; and (iii) female parasitoids exhibit a greater rate of increase in body size with host size than do male parasitoids. The observed patterns cannot be explained by sex-specific mortality of immature parasitoids developing on the different host size categories. In subsequent experiments, laboratory cultures ofC. grandisexposed daily to successively larger sizes ofA. grandislarvae produced successively greater female biased offspring sex ratios, cultures exposed daily to successively smaller sizes of host larvae produced successively greater male biased offspring sex ratios, and cultures exposed daily to equivalent host size distributions over time maintained a uniform offspring sex ratio. By increasing the average size ofA. grandislarval hosts exposed toC. grandisby 2.5 mg per day in mass rearing cultures, the percentage of male progeny can be reduced from 33% to 23% over a period of four consecutive exposure days.


Behaviour ◽  
1990 ◽  
Vol 114 (1-4) ◽  
pp. 137-147 ◽  
Author(s):  
H.C.J. Godfray ◽  
I.C.W. Hardy

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.


1993 ◽  
Vol 71 (5) ◽  
pp. 937-940 ◽  
Author(s):  
Barry N. Milligan ◽  
R. Mark Brigham

Sex allocation theory predicts that monomorphic species should produce natal sex ratios near unity. We measured natal sex ratios in a maternity colony of approximately 1600 yuma bats (Myotis yumanensis) near Squilax, British Columbia, during June and July 1991. Overall, the natal sex ratio did not differ from unity but the sex ratio did vary significantly throughout the summer. Variation appears to be related to an interaction between maternal age and date of birth. This evidence suggests that facultative manipulation of the sex of the offspring by individual females may occur within the population.


2020 ◽  
Author(s):  
Jun Abe ◽  
Ryosuke Iritani ◽  
Koji Tsuchida ◽  
Yoshitaka Kamimura ◽  
Stuart A. West

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.


2021 ◽  
Vol 118 (20) ◽  
pp. e2024656118
Author(s):  
Jun Abe ◽  
Ryosuke Iritani ◽  
Koji Tsuchida ◽  
Yoshitaka Kamimura ◽  
Stuart A. West

The puzzling sex ratio behavior of Melittobia wasps has long posed one of the greatest questions in the field of sex allocation. Laboratory experiments have found that, in contrast to the predictions of theory and the behavior of numerous other organisms, Melittobia females do not produce fewer female-biased offspring sex ratios when more females lay eggs on a patch. We solve this puzzle by showing that, in nature, females of Melittobia australica have a sophisticated sex ratio behavior, in which their strategy also depends on whether they have dispersed from the patch where they emerged. When females have not dispersed, they lay eggs with close relatives, which keeps local mate competition high even with multiple females, and therefore, they are selected to produce consistently female-biased sex ratios. Laboratory experiments mimic these conditions. In contrast, when females disperse, they interact with nonrelatives, and thus adjust their sex ratio depending on 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.


2021 ◽  
Vol 9 ◽  
Author(s):  
Max R. Lambert ◽  
Tariq Ezaz ◽  
David K. Skelly

Population sex ratio is a key demographic factor that influences population dynamics and persistence. Sex ratios can vary across ontogeny from embryogenesis to death and yet the conditions that shape changes in sex ratio across ontogeny are poorly understood. Here, we address this issue in amphibians, a clade for which sex ratios are generally understudied in wild populations. Ontogenetic sex ratio variation in amphibians is additionally complicated by the ability of individual tadpoles to develop a phenotypic (gonadal) sex opposite their genotypic sex. Because of sex reversal, the genotypic and phenotypic sex ratios of entire cohorts and populations may also contrast. Understanding proximate mechanisms underlying phenotypic sex ratio variation in amphibians is important given the role they play in population biology research and as model species in eco-toxicological research addressing toxicant impacts on sex ratios. While researchers have presumed that departures from a 50:50 sex ratio are due to sex reversal, sex-biased mortality is an alternative explanation that deserves consideration. Here, we use a molecular sexing approach to track genotypic sex ratio changes from egg mass to metamorphosis in two independent green frog (Rana clamitans) populations by assessing the genotypic sex ratios of multiple developmental stages at each breeding pond. Our findings imply that genotypic sex-biased mortality during tadpole development affects phenotypic sex ratio variation at metamorphosis. We also identified sex reversal in metamorphosing cohorts. However, sex reversal plays a relatively minor and inconsistent role in shaping phenotypic sex ratios across the populations we studied. Although we found that sex-biased mortality influences sex ratios within a population, our study cannot say at this time whether sex-biased mortality is responsible for sex ratio variation across populations. Our results illustrate how multiple processes shape sex ratio variation in wild populations and the value of testing assumptions underlying how we understand sex in wild animal populations.


2017 ◽  
Author(s):  
Alison B. Duncan ◽  
Cassandra Marinosci ◽  
Céline Devaux ◽  
Sophie Lefèvre ◽  
Sara Magalhães ◽  
...  

ABSTRACTThis preprint has been reviewed and recommended by Peer Community In Evolutionary Biology (https://doi.org/10.24072/pci.evolbiol.100051). In structured populations, competition for mates between closely related males, termed Local Mate Competition (LMC), is expected to select for female-biased offspring sex ratios. However, the cues underlying sex allocation decisions remain poorly studied. Here, we test for several cues in the spider mite Tetranychus urticae, a species that was previously found to adjust the sex ratio of its offspring in response to the number of females within the local population, i.e. a patch. We here investigate whether the offspring sex ratio of T. urticae females changes in response to 1) the current number of females in the same patch, 2) the number of females in the patches of their mothers and 3) their relatedness to their mate. Single females on patches produced similar sex ratios to those of groups of 15 females; their mothers had been in identical conditions of panmixia. The offspring sex ratios of females mated with their brother did not differ from those of females mated with an unrelated male. Females however produced a more female-biased offspring sex ratio if their mothers were alone on a patch compared to 15 other females. Thus, maternal environment is used as a cue for the sex allocation of daughters. We discuss the conditions under which the maternal environment may be a reliable predictor of LMC experienced by grand-sons.


2009 ◽  
Vol 5 (5) ◽  
pp. 682-685 ◽  
Author(s):  
David M. Shuker ◽  
Anna M. Moynihan ◽  
Laura Ross

Decisions over what sex ratio to produce can have far-reaching evolutionary consequences, for both offspring and parents. However, the extent to which males and females come into evolutionary conflict over aspects of sex allocation depends on the genetic system: when genes are passed to the next generation unequally by the two sexes (as in haplodiploidy, for example), this biased transmission can facilitate a range of conflicts not seen in diploids. However, much less attention has been paid to these forms of sexual conflict, not least because it has not always been clear how the conflicts could be realized. Here we consider how biased gene transmission, as expressed in different genetic systems, enhances the opportunity for sex ratio conflict and give empirical examples that confirm that males and females have the opportunity to influence sex ratios.


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