scholarly journals Endless Digging and Endless Picking. Sex Ratios and Gendered Labour in Surinamese Plantations, 1830–1863

2021 ◽  
Vol 10 ◽  
pp. 46-52
Author(s):  
Cornelis W. Van Galen ◽  
Björn Quanjer ◽  
Matthias Rosenbaum-Feldbrügge ◽  
Matthijs Kraijo
Keyword(s):  
Sex Ratio ◽  
Age Structure ◽  
Excess Mortality ◽  
Sex Ratios ◽  
Division Of Labour ◽  
Historical Database ◽  
Broad Overview

In this article we study the question why the sex ratio among the enslaved population of plantation workers reversed from a male to a female surplus between 1830 and the abolition of slavery in 1863. We use the Historical Database of Suriname (HDS) to answer this question in three steps. First, we give a broad overview of the changing sex ratios in the various Surinamese regions between 1838 and 1861. Second, we study the age structure on three plantations in the district Coronie in 1830 in detail. Finally, we use muster rolls available for the Catharina Sophia plantation in the period 1848–1849 to analyse the gendered division of labour. Our results indicate that both the male surpluses during the 1830s and the subsequent skew of the sex ratios towards females were the effects of a gendered division of labour, in which plantation managers preferred male labourers for heavy and unhealthy work in the construction and upkeep of plantation polders. This led to an excess mortality of enslaved men.

scholarly journals Line-transect data may not produce reliable estimates of interannual sex-ratio and age structure variation in West African savannah ungulates

2020 ◽  
Vol 33 (1) ◽  
Author(s):  
Emmanuel M. Hema ◽  
Yaya Ouattara ◽  
Maomarco Abdoul Ismael Tou ◽  
Giovanni Amori ◽  
Mamadou Karama ◽  
...  
Keyword(s):  
Sex Ratio ◽  
Age Structure ◽  
A Priori ◽  
Sex Ratios ◽  
West African ◽  
Line Transect ◽  
Structure Variation ◽  
Line Transects ◽  
Observed Score ◽  
Age Structures

Adult sex ratios and age structures are important wildlife population parameters, but they have been poorly investigated in ungulate species in West African savannahs. We used line transects to investigate these parameters in 11 ungulates from a protected area in south-western Burkina Faso during the period 2010-2018. We created an empirical model of “detectability” for each species based on its main ecological characteristics (habitat and group size) and body size, and then compared the observed interannual inconsistency in sex ratios and age structures with the a priori detectability score. Six out of 11 species showed low interannual inconsistency in sex ratio and age structure. In 82% of the study species, however, the predicted detectability score matched the observed score, with two exceptions being Tragelaphus scriptus and Sincerus caffer.

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.

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 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. 

scholarly journals Statistical Study Of The Sex Ratio At Birth

1936 ◽  
Vol 36 (3) ◽  
pp. 381-401 ◽  
Author(s):  
W. T. Russell
Keyword(s):  
Sex Ratio ◽  
Excess Mortality ◽  
Statistical Study ◽  
Experimental Studies ◽  
Vital Statistics ◽  
Conception Rate ◽  
Sex Ratio At Birth ◽  
Live Births ◽  
Natal Mortality

That the number of male births always exceeds that of females is well known to students of vital statistics, but the biological law responsible for the phenomenon has not yet been adequately determined though various theories have been offered in explanation. It has been suggested that it resulted from a high male conception rate which, although modified by an excess mortality of male embryos, nevertheless produced a masculinity of matured births. In more recent times the conclusions drawn by MacDowell & Lord (1925, 1925 a) from their experimental studies with mice have failed to support this view. They claimed that there was no correlation between the pre-natal mortality and the masculinity of live births, that the primary ratio at conception was almost identical with that at birth. These contentions were criticized by Parkes (1923, 1926), who, whilst maintaining the doctrine that the ante-natal mortality of mice “falls preponderatingly upon the males”, stated “that it is quite obvious that a great deal more information is required before any coherent story of the factors governing the sex ratio at birth in the mouse (and all other mammals) can be put together”.

A new male-killing parasitism:Spiroplasmabacteria infect the ladybird beetleAnisosticta novemdecimpunctata(Coleoptera: Coccinellidae)

Parasitology ◽  
2006 ◽  
Vol 132 (6) ◽  
pp. 757-765 ◽  
Author(s):  
M. C. TINSLEY ◽  
M. E. N. MAJERUS
Keyword(s):  
Phylogenetic Analysis ◽  
Sex Ratio ◽  
High Efficiency ◽  
Sex Ratios ◽  
Egg Hatch ◽  
Hatch Rate ◽  
Male Killing ◽  
Offspring Sex ◽  
Novel Host ◽  
Males And Females

Whilst most animals invest equally in males and females when they reproduce, a variety of vertically transmitted parasites has evolved the ability to distort the offspring sex ratios of their hosts. One such group of parasites are male-killing bacteria. Here we report the discovery of females of the ladybirdAnisosticta novemdecimpunctatathat produced highly female-biased offspring sex ratios associated with a 50% reduction in egg hatch rate. This trait was maternally transmitted with high efficiency, was antibiotic sensitive and was infectious following experimental haemolymph injection. We identified the cause as a male-killingSpiroplasmabacterium and phylogenetic analysis of rDNA revealed that it belongs to theSpiroplasma ixodetisclade in which other sex ratio distorters lie. We tested the potential for interspecific horizontal transfer by injection from an infectedA. novemdecimpunctataline into uninfected individuals of the two-spot ladybirdAdalia bipunctata. In this novel host, the bacterium was able to establish infection, transmit vertically and kill male embryos.

scholarly journals Some aspects of the history and population ecology of the tsessebe damaliscus lunatus lunatus in the Kruger National Park

Koedoe ◽  
1977 ◽  
Vol 20 (1) ◽  
Author(s):  
S.C.J. Joubert ◽  
P.J.L. Bronkhorst
Keyword(s):  
Sex Ratio ◽  
Population Ecology ◽  
Age Structure ◽  
National Park ◽  
Kruger National Park ◽  
Population Trends ◽  
Social Organisation ◽  
Developmental History ◽  
The Social ◽  
History Of

The population trends and distribution of the tsessebe population of the Kruger National Park are evaluated in terms of the available data derived from records compiled in the developmental history of the Kruger National Park (KNP). The recent numerical status of the population is also given. A description of the habitats favoured by tsessebe in the KNP is presented as well as an analysis of the age structure and sex-ratio of the population. Aspects of the social organisation of tsessebe affecting the interpretation of the age structure and sex-ratio phenomena of the population, are also discussed.

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