scholarly journals Adult sex ratios and their implications for cooperative breeding in birds

2017 ◽  
Vol 372 (1729) ◽  
pp. 20160322 ◽  
Author(s):  
Jan Komdeur ◽  
Tamás Székely ◽  
Xiaoyan Long ◽  
Sjouke A. Kingma
Keyword(s):  
Sex Ratio ◽  
Cooperative Breeding ◽  
Adult Population ◽  
Sex Ratios ◽  
Bird Species ◽  
Dispersal Distance ◽  
Sex Bias ◽  
Wide Range ◽  
Cooperatively Breeding ◽  
Using Data

Cooperative breeding is a form of breeding system where in addition to a core breeding pair, one or more usually non-breeding individuals provide offspring care. Cooperative breeding is widespread in birds, but its origin and maintenance in contemporary populations are debated. Although deviations in adult sex ratio (ASR, the proportion of males in the adult population) have been hypothesized to influence the occurrence of cooperative breeding because of the resulting surplus of one sex and limited availability of breeding partners, this hypothesis has not been tested across a wide range of taxa. By using data from 188 bird species and phylogenetically controlled analyses, we show that cooperatively breeding species have more male-biased ASRs than non-cooperative species. Importantly, ASR predicts helper sex ratio: in species with more male-biased ASR, helper sex ratio is also more male biased. We also show that offspring sex ratios do not predict ASRs, so that the skewed ASRs emerge during the period when individuals aim to obtain a breeding position or later during adulthood. In line with this result, we found that ASR (among both cooperatively and non-cooperatively breeding species) is inversely related to sex bias in dispersal distance, suggesting that the cost of dispersal is more severe for the further-dispersing sex. As females usually disperse further in birds, this explains the generally male-biased ASR, and in combination with benefits of philopatry for males, this probably explains why ASR is more biased in cooperatively breeding species. Taken together, our results suggest that a sex bias in helping in cooperatively breeding species relates to biased ASRs. We propose that this relationship is driven by sex-specific costs and benefits of dispersal and helping, as well as other demographic factors. Future phylogenetic comparative and experimental work is needed to establish how this relationship emerges. 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’.

scholarly journals Sex Allocation, Diet, and Small Population Management of African Rhinoceros

2021 ◽  
Author(s):  
◽  
Elizabeth Victoria Berkeley
Keyword(s):  
Sex Ratio ◽  
Population Growth ◽  
Survival Probability ◽  
Sex Allocation ◽  
Sex Ratios ◽  
Small Population ◽  
Ex Situ ◽  
Sex Bias ◽  
Theoretic Approach ◽  
Wet Season

<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>

THE ENIGMA OF ETHIOPIAN SEX RATIOS AT BIRTH

2016 ◽  
Vol 49 (5) ◽  
pp. 611-622
Author(s):  
Michel Garenne
Keyword(s):  
Sex Ratio ◽  
Urban Areas ◽  
Maternal Education ◽  
Sex Ratios ◽  
Household Wealth ◽  
Poor Nutritional Status ◽  
Linguistic Groups ◽  
Children Ever Born ◽  
Using Data ◽  
The Many

SummaryThis study analysed sex ratios at birth (defined as the number of male births per 100 female births) using data on children ever-born from three censuses conducted in Ethiopia in 1984, 1994 and 2007. The results showed very high values by any standard, with an average of 108.4 for a sample of some 8.2 million births, with somewhat lower values in urban areas. Analysis of socioeconomic correlates revealed that the sex ratio varied very much by household wealth, from about 110 for very poor women to about 102 for wealthier women. The high value of the sex ratio at birth in Ethiopia could be explained by poverty, used as a proxy for poor nutritional status. In multivariate analysis, the effects of living in urban areas and of maternal education were less important than household wealth. Among the many ethno-linguistic groups, the Nilotic family had higher sex ratios than other groups. The results were confirmed using data from DHS surveys conducted in the country, and by the analysis of children still living at time of census.

scholarly journals Climate predicts which sex acts as helpers among cooperatively breeding bird species

2017 ◽  
Vol 13 (1) ◽  
pp. 20160863 ◽  
Author(s):  
Guoyue Zhang ◽  
Qingtian Zhao ◽  
Anders Pape Møller ◽  
Jan Komdeur ◽  
Xin Lu
Keyword(s):  
Bird Species ◽  
Adult Survival ◽  
Sex Bias ◽  
Tropical Species ◽  
Ecological Constraints ◽  
Breeding Bird ◽  
Adult Females ◽  
Cooperatively Breeding ◽  
Demographic Response ◽  
Potential Determinant

Among avian cooperative breeders, help in raising offspring is usually provided by males or by both sexes. Sex bias in helping should evolve in response to sex-specific ecological constraints on independent reproduction, with mate shortage for males and breeding vacancy shortage for each sex. Given that male-biased adult sex ratios are prevalent among birds, we predict that male-only helping mainly occurs in temperate species where fast population turnovers deriving from low adult annual survival allow all adult females to hold breeding vacancies, whereas some males overflow as helpers, and both-sex helping in tropical species where saturated habitats prevent not only males, but also females from breeding themselves. As expected, we found that across species, adult survival increased towards tropical zones and warmer climates, and higher adult survival tended to be associated with both-sex helping. Furthermore, sex bias in helping was predicted by latitude and ambient temperature. Our findings of demographic response of species to climate as a potential determinant of bias in helper sex uncover how ecological constraints operate to limit independent reproduction in sex-specific ways.

scholarly journals Estimating adult sex ratios in nature

2017 ◽  
Vol 372 (1729) ◽  
pp. 20160313 ◽  
Author(s):  
Sergio Ancona ◽  
Francisco V. Dénes ◽  
Oliver Krüger ◽  
Tamás Székely ◽  
Steven R. Beissinger
Keyword(s):  
Sex Differences ◽  
Sex Ratio ◽  
Evolutionary Biology ◽  
Adult Population ◽  
Sex Ratios ◽  
Estimation Methods ◽  
Spatial And Temporal Variation ◽  
Animal Populations ◽  
Adult Sex Ratio ◽  
Males And Females

Adult sex ratio (ASR, the proportion of males in the adult population) is a central concept in population and evolutionary biology, and is also emerging as a major factor influencing mate choice, pair bonding and parental cooperation in both human and non-human societies. However, estimating ASR is fraught with difficulties stemming from the effects of spatial and temporal variation in the numbers of males and females, and detection/capture probabilities that differ between the sexes. Here, we critically evaluate methods for estimating ASR in wild animal populations, reviewing how recent statistical advances can be applied to handle some of these challenges. We review methods that directly account for detection differences between the sexes using counts of unmarked individuals (observed, trapped or killed) and counts of marked individuals using mark–recapture models. We review a third class of methods that do not directly sample the number of males and females, but instead estimate the sex ratio indirectly using relationships that emerge from demographic measures, such as survival, age structure, reproduction and assumed dynamics. We recommend that detection-based methods be used for estimating ASR in most situations, and point out that studies are needed that compare different ASR estimation methods and control for sex differences in dispersal. 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’.

SEX RATIO AT BIRTH AND FAMILY COMPOSITION IN SUB-SAHARAN AFRICA: INTER-COUPLE VARIATIONS

2009 ◽  
Vol 41 (3) ◽  
pp. 399-407 ◽  
Author(s):  
MICHEL GARENNE
Keyword(s):  
Sex Ratio ◽  
Sex Ratios ◽  
The United States ◽  
Sub Saharan Africa ◽  
Family Composition ◽  
Sex Ratio At Birth ◽  
First Birth ◽  
Wide Range ◽  
Sub Saharan ◽  
Linear Logistic Model

SummaryIn this study, sex ratios at birth (male/female births) were found to vary according to family composition. Using Demographic and Health Survey (DHS) maternity histories from sub-Saharan Africa, the study shows that the sex ratio at birth increases with the number of previous male births and decreases with the number of previous female births. For families with only males, the sex ratio increases from 1·046 for the first birth to 1·083 for the 8th birth. For families with only females, the sex ratio decreases from 1·046 for the first birth to 0·942 for the 8th birth. The differences were highly significant when tested with a linear logistic model (p=0·018 for males; p=1·85✕10−11 for females). The effect was not symmetrical, and was found to be significantly stronger for females. These effects could be reproduced assuming a strong heterogeneity between couples. The distribution of sex ratios was fitted with an asymmetrical log-gamma function, which revealed a wide range of variation in the sex ratio between 0·50 and 1·30, and a peak around 1·14. The results and their implications are discussed in the light of former findings in France and in the United States of America.

Population structure and the evolution of sexual size dimorphism and sex ratios in an insular population of Florida box turtles (Terrapene Carolina bauri)

1997 ◽  
Vol 75 (9) ◽  
pp. 1495-1507 ◽  
Author(s):  
C. Kenneth Dodd Jr.
Keyword(s):  
Sex Ratio ◽  
Sexual Size Dimorphism ◽  
Sex Ratios ◽  
Size Dimorphism ◽  
Terrapene Carolina ◽  
Key Population ◽  
Younger Age ◽  
Box Turtles ◽  
The Status ◽  
Using Data

Hypotheses in the chelonian literature suggest that in species with sexual size dimorphism, the smaller sex will mature at a smaller size and a younger age than the larger sex, sex ratios should be biased in favor of the earlier maturing sex, and deviations from a 1:1 sex ratio result from maturation of the smaller sex at a younger age. I tested these hypotheses using data collected from 1991 to 1995 on an insular (Egmont Key) population of Florida box turtles, Terrapene Carolina bauri. Contrary to predictions, the earlier maturing sex (males) grew to larger sizes than the late maturing sex. Males were significantly larger than females in mean carapace length but not mean body mass. Sex ratios were not balanced, favoring the earlier maturing sex (1.6 males: 1 female), but the sex-ratio imbalance did not result from faster maturation of the smaller sex. The imbalance in the sex ratio in Egmont Key's box turtles is not the result of sampling biases; it may result from nest placement. Size-class structure and sex ratios can provide valuable insights into the status and trends of populations of long-lived turtles.

A model to explain the replacement of Schistosoma intercalatum by Schistosoma haematobium and the hybrid S. intercalatum×S. haematobium in areas of sympatry

Parasitology ◽  
2002 ◽  
Vol 124 (4) ◽  
pp. 401-408 ◽  
Author(s):  
S. MORAND ◽  
V. R. SOUTHGATE ◽  
J. JOURDANE
Keyword(s):  
Mathematical Model ◽  
Sex Ratio ◽  
Schistosoma Haematobium ◽  
Field Data ◽  
Sex Ratios ◽  
Sex Bias ◽  
Simple Mathematical Model ◽  
Schistosoma Intercalatum

Numerous hypotheses have been postulated to explain the rapidly changing parasitological situation in Loum, Cameroon as a result of the interaction between Schistosoma haematobium and S. intercalatum. The aim of this study is to test the various hypotheses using a simple mathematical model, incorporating equal and unequal sex ratios of adult schistosomes, recombinations, and levels of compatibility with the intermediate molluscan hosts, B. forskalii and B. truncatus. The model assuming an equal sex ratio does not fit with the existing field data in that it predicts a continued presence of S. intercalatum, S. haematobium and the hybrids. The model assuming a sex bias in favour of males, which reflects the situation usually observed in schistosome populations, predicts the loss S. intercalatum which indeed concurs with the most recent data.

scholarly journals Sex Allocation, Diet, and Small Population Management of African Rhinoceros

2021 ◽  
Author(s):  
◽  
Elizabeth Victoria Berkeley
Keyword(s):  
Sex Ratio ◽  
Population Growth ◽  
Survival Probability ◽  
Sex Allocation ◽  
Sex Ratios ◽  
Small Population ◽  
Ex Situ ◽  
Sex Bias ◽  
Theoretic Approach ◽  
Wet Season

<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>

scholarly journals Climate-driven shifts in adult sex ratios via sex reversals: the type of sex determination matters

2017 ◽  
Vol 372 (1729) ◽  
pp. 20160325 ◽  
Author(s):  
Veronika Bókony ◽  
Szilvia Kövér ◽  
Edina Nemesházi ◽  
András Liker ◽  
Tamás Székely
Keyword(s):  
Sex Ratio ◽  
Sex Determination ◽  
Sex Ratios ◽  
Theoretical Models ◽  
Reproductive Decisions ◽  
Adult Sex Ratio ◽  
Survival And Reproduction ◽  
Opposite Sex ◽  
Using Data ◽  
Heterogametic Sex

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’.

scholarly journals Sex-specific deaths in Norway and Sweden during the COVID-19 pandemic: Did mandates make a difference?

2021 ◽  
pp. 140349482110100
Author(s):  
Ralph Catalano
Keyword(s):  
Sex Ratio ◽  
Infection Control ◽  
Temporal Variation ◽  
Risky Behavior ◽  
Control Strategies ◽  
Sex Ratios ◽  
Female Mortality ◽  
All Cause Mortality ◽  
Societal Expectations ◽  
Male To Female

Aims: To determine whether differences between Norway’s and Sweden’s attempts to contain SARS-CoV-2 infection coincided with detectably different changes in their all-cause mortality sex ratios. Measuring temporal variation in the all-cause mortality sex ratio before and during the pandemic in populations exposed to different constraints on risky behavior would allow us to better anticipate changes in the ratio and to better understand its association with infection control strategies. Methods: I apply time Box–Jenkins modeling to 262 months of pre-pandemic mortality sex ratios to arrive at counterfactual values of 10 intra-pandemic ratios. I compare counterfactual to observed values to determine if intra-pandemic ratios differed detectably from those expected as well as whether the Norwegian and Swedish differences varied from each other. Results: The male to female mortality sex ratio in both Norway and Sweden increased during the pandemic. I, however, find no evidence that the increase differed between the two countries despite their different COVID-19 containment strategies. Conclusion: Societal expectations of who will die during the COVID-19 pandemic will likely be wrong if they assume pre-pandemic mortality sex ratios because the intra-pandemic ratios appear, at least in Norway and Sweden, detectably higher. The contribution of differences in policies to reduce risky behavior to those higher ratios appears, however, small.

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