Sex ratio estimation and survival analysis for Orthetrum coerulescens (Odonata, Libellulidae)

2004 ◽  
Vol 82 (3) ◽  
pp. 399-406 ◽  
Author(s):  
M Kéry ◽  
L Juillerat
Keyword(s):  
Sex Ratio ◽  
Sex Ratios ◽  
Survival Rates ◽  
Activity Period ◽  
Time Interval ◽  
Ratio Estimation ◽  
Capture Recapture ◽  
Specific Variation ◽  
Population Survival ◽  
Time Specific

There is controversy over whether uneven sex ratios observed in mature dragonfly populations are a mere artifact resulting from the higher observability of males. Previous studies have at best made indirect inference about sex ratios by analysis of survival or recapture rates. Here, we obtain direct estimates of sex ratio from capture–recapture data based on the Cormack–Jolly–Seber model. We studied Orthetrum coerulescens (Fabricius, 1798) at three sites in the Swiss Jura Mountains over an entire activity period. Recapture rates per 5-day interval were 3.5 times greater for males (0.67, SE 0.02) than for females (0.19, SE 0.02). At two sites, recapture rate increased over the season for males and was constant for females, and at one site it decreased with precipitation for both sexes. In addition, recapture rate was higher with higher temperature for males only. We found no evidence for higher male survival rates in any population. Survival per 5-day interval for both sexes was estimated to be 0.77 (95% CI 0.75–0.79) without significant site-or time-specific variation. There were clear effects of temperature (positive) and precipitation (negative) on survival rate at two sites. Direct estimates of sex ratios were not significantly different from 1 for any time interval. Hence, the observed male-biased sex ratio in adult O. coerulescens was an artifact resulting from the better observability of males. The method presented in this paper is applicable to sex ratio estimation in any kind of animal.

scholarly journals BROODSTOCK SEX RATIO IMPROVES FRY PRODUCTION IN NILE TILAPIA(OREOCHROMIS NILOTICUS) IN NORTHERN SENEGAL

2021 ◽  
Vol 9 (02) ◽  
pp. 72-76
Author(s):  
Mouhamadou Amadou Ly ◽  
◽  
Abdoulaye Ngom ◽  
Ahmadou Bamba Fall ◽  
Ousmane Diouf ◽  
...  
Keyword(s):  
Sex Ratio ◽  
Oreochromis Niloticus ◽  
Nile Tilapia ◽  
Sex Ratios ◽  
Survival Rates ◽  
Fish Farming ◽  
Commercial Diet ◽  
Ph Values ◽  
Nile Tilapia Oreochromis Niloticus ◽  
Female Survival

This present study was conducted to determine fry production in different male-female sex ratios of Oreochromis niloticusbroodstock in order to improve fry production, which handicapped the development of fish farming in northern Senegal. A total of 180 broodfish (47 males and 133 females) were stocked at a density of 2 fish /m2and was replicated three times for each sex ratio of 1:2, 1:3and 1:4 (male : female). Mean body weight ranges from 136.47±2.13 and 107.27±2.14 g for female and male O. niloticusbroodstock, respectively. The experiment was conducted for 90 days and the broods were fed on commercial diet containing 32% crude protein.Fish were held in 9 rectangular tanks of 30 m3 each (10 × 3 × 1) and half-filled. The results showed that number of fry produced at different sex ratios were significantly different, with sex ratio of 1:2 producing a highest number of fry (279.67) per female, followed by the 1:3and 1:4 treatment recorded the lowest.Broodstock sex ratios also did not affect female survival rates and all treatments had 100% survival rates. Temperature, dissolved oxygen and pH values obtained were suitable for good water quality and normal tilapia reproduction.In conclusion, the results of the present study recommend to stock Oreochromis niloticus brooders when stocked at a density of 2 fish /m2 at a sex ratio of 1 male : 2 female in order to obtain the highest fry production.

Common vole (Microtus arvalis) population sex ratio: biases and process variation

2005 ◽  
Vol 83 (11) ◽  
pp. 1391-1399 ◽  
Author(s):  
Josef Bryja ◽  
Jiřina Nesvadbová ◽  
Marta Heroldová ◽  
Eva Jánová ◽  
Jan Losík ◽  
...  
Keyword(s):  
Sex Ratio ◽  
Process Variation ◽  
Methodological Approach ◽  
Survival Rates ◽  
Common Vole ◽  
Joint Effect ◽  
Microtus Arvalis ◽  
Differential Survival ◽  
Capture Recapture ◽  
Error Bias

Vole population sex ratio varies seasonally. However, population sex ratios have usually been estimated using naïve estimators that do not allow for biases owing to the sex difference in capture probabilities and movement distances (i.e., effective areas sampled). Here we aimed to advance the methodological approach, recognizing that there are two different classes of contributing mechanisms to the pattern which are best addressed separately: (1) those mechan isms imposing a systematic error (bias) in population estimates and (2) those generating the true process variation. Analyzing 7-year capture–recapture data in the common vole (Microtus arvalis (Pallas, 1778)), we quantified both types of biases and revealed that the bias owing to differential capture rates was often severe and less predictable, whereas that owing to differential effective areas was smaller and overestimated male numbers for most of the year. We demonstrated unambiguously that the unbiased population sex ratio indeed varies seasonally, with the males usually being more numerous over winter and spring. By testing predictions from two mechanistic hypotheses to explain the process variability, we found evidence for both the differential recruitment hypothesis and the differential survival hypothesis. From April–May to August, it was the females that were recruited more to the population and that had higher survival rates than males. We suggest that the seasonal variation in the population sex ratio is not merely a result of biasing mechanisms but an important population property driven by the joint effect of differential recruitment and differential survival between sexes.

scholarly journals Instrumented individuals are not representative of the population. Survival of wolverines with and without GPS collars

2020 ◽  
Author(s):  
Cyril Milleret ◽  
Richard Bischof ◽  
Pierre Dupont ◽  
Henrik Brøseth ◽  
John Odden ◽  
...  
Keyword(s):  
Survival Rates ◽  
Population Level ◽  
Large Carnivores ◽  
Gps Collars ◽  
Positive Effects ◽  
Non Invasive ◽  
Open Population ◽  
Capture Recapture ◽  
Population Survival ◽  
Using Data

AbstractResults from biologging studies are often scaled up to population-level inferences and this begs the question: Are instrumented animals representative of the population given the potential bias in individual selectivity, the influence of capture, handling and wearing bio-loggers? The answer is elusive due to the challenges of obtaining comparable data from individuals without bio-loggers. Using non-invasive genetic data of a large carnivore, the wolverine (Gulo gulo) in Scandinavia, and an open-population spatial capture-recapture model, we were able to estimate and compare survival rates of individuals fitted with GPS collars versus individuals that had never been captured and collared. We found that mortality of GPS collared individuals was 47% lower compared to individuals without GPS collars. While instrumented and non-instrumented wolverines had similar risks of dying from legal culling, GPS collared individuals displayed lower mortality rates due to causes other than legal culling. Reports of positive effects of biologging on the fitness of individuals are rather uncommon and we argue that the most likely explanation is that GPS-collars could shield animals from poaching. Our results highlight the challenges of drawing population level inferences for large carnivores when using data from an instrumented sample of the population.

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. 

TIME-SPECIFIC VARIATION IN PASSERINE NEST SURVIVAL: NEW INSIGHTS INTO OLD QUESTIONS

The Auk ◽  
2005 ◽  
Vol 122 (2) ◽  
pp. 661 ◽  
Author(s):  
Todd A. Grant ◽  
Terry L. Shaffer ◽  
Elizabeth M. Madden ◽  
Pamela J. Pietz
Keyword(s):  
Nest Survival ◽  
Specific Variation ◽  
Time Specific

Status of the Hawaiian monk seal (Monachus schauinslandi) population

1995 ◽  
Vol 73 (6) ◽  
pp. 1185-1190 ◽  
Author(s):  
W. G. Gilmartin ◽  
L. L. Eberhardt
Keyword(s):  
Complex System ◽  
Sex Ratios ◽  
Current Trend ◽  
Survival Rates ◽  
Hawaiian Monk Seal ◽  
Monachus Schauinslandi ◽  
Young Females ◽  
Adult Females ◽  
Unknown Factor ◽  
Adult Sex Ratio

Restoration of the Hawaiian monk seal (Monachus schauinslandi) population to its former abundance poses a number of problems in managing a complex system. Sharp differences in history and current trend exist among the six major pupping sites. A severely unbalanced adult sex ratio has resulted in deaths from "mobbing" of estrus females at two sites. Some unknown factor apparently severely reduced the numbers of females at three of the sites and thus produced the observed excess of males. Sex ratios subsequently decreased, but losses of adult females continue at two sites. A simple model indicates that sex ratios at the two sites where mobbing is a problem would require more than 10 years to approach an equilibrium value. Data on trends from counts are compared with estimates from reproduction and survival rates and agree closely except at one site (Kure Atoll), where introductions of young females have been made.

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