Effects of photoperiod on offspring production, development and generation time, survival, adult sex ratio and total life span of freshwater cyclopoid copepod,Mesocyclopssp.: comments on individual variations

2013 ◽  
Vol 46 (1) ◽  
pp. 163-172 ◽  
Author(s):  
Abolghasem Esmaeili Fereidouni ◽  
Samaneh Meskar ◽  
Shima Masoudi Asil
Keyword(s):  
Sex Ratio ◽  
Life Span ◽  
Generation Time ◽  
Cyclopoid Copepod ◽  
Offspring Production ◽  
Production Development ◽  
Individual Variations ◽  
Adult Sex Ratio ◽  
Total Life

scholarly journals Not all sex ratios are equal: the Fisher condition, parental care and sexual selection

2017 ◽  
Vol 372 (1729) ◽  
pp. 20160312 ◽  
Author(s):  
Michael D. Jennions ◽  
Lutz Fromhage
Keyword(s):  
Sex Differences ◽  
Sex Ratio ◽  
Parental Care ◽  
Sex Roles ◽  
Sex Role ◽  
Sex Ratios ◽  
Theoretical Models ◽  
Evolution Of Sex ◽  
Offspring Production ◽  
Adult Sex Ratio

The term ‘sex roles’ encapsulates male–female differences in mate searching, competitive traits that increase mating/fertilization opportunities, choosiness about mates and parental care. Theoretical models suggest that biased sex ratios drive the evolution of sex roles. To model sex role evolution, it is essential to note that in most sexually reproducing species (haplodiploid insects are an exception), each offspring has one father and one mother. Consequently, the total number of offspring produced by each sex is identical, so the mean number of offspring produced by individuals of each sex depends on the sex ratio (Fisher condition). Similarly, the total number of heterosexual matings is identical for each sex. On average, neither sex can mate nor breed more often when the sex ratio is even. But equally common in which sex ratio? The Fisher condition only applies to some reproductive measures (e.g. lifetime offspring production or matings) for certain sex ratios (e.g. operational or adult sex ratio; OSR, ASR). Here, we review recent models that clarify whether a biased OSR, ASR or sex ratio at maturation (MSR) have a causal or correlational relationship with the evolution of sex differences in parental care and competitive traits—two key components of sex roles. We suggest that it is more fruitful to understand the combined effect of the MSR and mortality rates while caring and competing than that of the ASR itself. In short, we argue that the ASR does not have a causal role in the evolution of parental care. We point out, however, that the ASR can be a cue for adaptive phenotypic plasticity in how each sex invests in parental care. 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’.

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.

scholarly journals Sex ratio effects on reproductive strategies in humans

2015 ◽  
Vol 2 (1) ◽  
pp. 140402 ◽  
Author(s):  
Ryan Schacht ◽  
Monique Borgerhoff Mulder
Keyword(s):  
Sexual Selection ◽  
Sex Ratio ◽  
Ethnic Group ◽  
Reproductive Strategies ◽  
Situational Factors ◽  
Male Mating ◽  
Mating Effort ◽  
Short Term ◽  
Adult Sex Ratio ◽  
Using Data

Characterizations of coy females and ardent males are rooted in models of sexual selection that are increasingly outdated. Evolutionary feedbacks can strongly influence the sex roles and subsequent patterns of sex differentiated investment in mating effort, with a key component being the adult sex ratio (ASR). Using data from eight Makushi communities of southern Guyana, characterized by varying ASRs contingent on migration, we show that even within a single ethnic group, male mating effort varies in predictable ways with the ASR. At male-biased sex ratios, men's and women's investment in mating effort are indistinguishable; only when men are in the minority are they more inclined towards short-term, low investment relationships than women. Our results support the behavioural ecological tenet that reproductive strategies are predictable and contingent on varying situational factors.

scholarly journals Is biasing offspring sex ratio adaptive? A test of Fisher's principle across multiple generations of a wild mammal in a fluctuating environment

2018 ◽  
Vol 285 (1891) ◽  
pp. 20181251 ◽  
Author(s):  
Andrea E. Wishart ◽  
Cory T. Williams ◽  
Andrew G. McAdam ◽  
Stan Boutin ◽  
Ben Dantzer ◽  
...  
Keyword(s):  
Sex Ratio ◽  
Tamiasciurus Hudsonicus ◽  
Red Squirrels ◽  
Offspring Sex Ratio ◽  
Offspring Sex ◽  
Adult Sex Ratio ◽  
Secondary Sex Ratio ◽  
North American Red Squirrels ◽  
Negative Frequency Dependent Selection ◽  
Fisher’S Principle

Fisher's principle explains that population sex ratio in sexually reproducing organisms is maintained at 1 : 1 owing to negative frequency-dependent selection, such that individuals of the rare sex realize greater reproductive opportunity than individuals of the more common sex until equilibrium is reached. If biasing offspring sex ratio towards the rare sex is adaptive, individuals that do so should have more grandoffspring. In a wild population of North American red squirrels ( Tamiasciurus hudsonicus ) that experiences fluctuations in resource abundance and population density, we show that overall across 26 years, the secondary sex ratio was 1 : 1; however, stretches of years during which adult sex ratio was biased did not yield offspring sex ratios biased towards the rare sex. Females that had litters biased towards the rare sex did not have more grandoffspring. Critically, the adult sex ratio was not temporally autocorrelated across years, thus the population sex ratio experienced by parents was independent of the population sex ratio experienced by their offspring at their primiparity. Expected fitness benefits of biasing offspring sex ratio may be masked or negated by fluctuating environments across years, which limit the predictive value of the current sex ratio.

scholarly journals Biology of Diadiplosis multifila (Diptera: Cecidomyiidae) in Planococcus citri under constant temperatures

2019 ◽  
Vol 10 (3) ◽  
pp. 346-352
Author(s):  
Alexandre Martins Dos Santos ◽  
José Eudes De Morais Oliveira ◽  
Andréa Nunes Moreira de Carvalho ◽  
Martin Duarte De Oliveira ◽  
Carla Patrícia Oliveira de Assis ◽  
...  
Keyword(s):  
Life Cycle ◽  
Sex Ratio ◽  
Larval Stage ◽  
Pupal Stage ◽  
Planococcus Citri ◽  
Egg Viability ◽  
Northeast Region ◽  
Embryonic Period ◽  
Semi Arid ◽  
Total Life

Diadiplosis multifila was recently discovered feeding on Planococcus citri eggs in vineyards in the semi-arid northeast region of Brazil. The objective of the present paper was to study the biology of D. multifila in P. citri under constant temperatures of 22, 25, 28, and 31 °C. We evaluated its embryonic stage, egg viability, development period, survival of larva and pupa, longevity, average number of eggs, and sex ratio. D. multifila completed its life cycle in all temperatures except for 31 °C. The length of the embryonic period ranged from 4 to 7 days. The larval stage was longer at a temperature of 22 °C (8.6 days) and shorter at 28 °C (6.4). The pupal stage exhibited durations of 12.9, 10.4, and 8.2 days for temperatures of 22, 25, and 28 °C, respectively. The average viability in the larval stage was 97% and 83% in the pupal stage. The total life cycle took 16.7 (28 °C), 20 (25 °C), and 27 (22 °C) days to complete. The adults lived for approximately 2 days and the females produced on average 34, 25, and 19 eggs at temperatures of 22, 25, and 28 °C, respectively. The sex ratio varied from 0.46 to 0.54.

scholarly journals Biology of pink stem borer, Sesamia inferens (Walker) on maize, Zea mays

2017 ◽  
Vol 9 (4) ◽  
pp. 1994-2003
Author(s):  
Hemant Sharma ◽  
Maha Singh Jaglan ◽  
S. S. Yadav
Keyword(s):  
Life Span ◽  
First Generation ◽  
Insect Pest ◽  
Management Strategies ◽  
Stem Borer ◽  
Adult Longevity ◽  
Research Station ◽  
Sesamia Inferens ◽  
Two Generations ◽  
Total Life

Biology of pink stem borer, Sesamia inferens (Walker) (Lepidoptera: Noctuidae) was conducted during 2015-16 in laboratories of CCS Haryana Agricultural University, Regional Research Station, Karnal on HQPM 1 (hybrid) and HKI 1128 (inbred) for two generations at room temperature. Results on biology of S. inferens in the first generation revealed that incubation period varied from 10-14 days on HQPM 1 and 11-15 days on HKI 1128. The larval duration lasted for 21-37 days on HQPM 1 and 24-39 days on HKI 1128. The adult longevity of male and female ranged from 6-7 days and 7-8 days on HQPM 1 and 5-7 days and 6-7 days on HKI 1128, respectively. The total life span ranged from 63-72 days for female and 45-58 days for male on HQPM 1 and 65-74 days for female and 49-62 days for male on HKI 1128, respectively in the first generation. The total life span in second generation ranged 94-107 days for female and 83-96 days for male on HQPM 1 and 98-112 days for female and 86-101 days for male on HKI 1128. The biology of an insect pest is a condition precedent to find out its management strategies. The biology of S. inferens on maize has not yet been studied in north western part of the country. Having regards to the fact that no systematic work on this aspect has been carried out, studies were conducted on biology of this pest for developing efficient pest management strategies.

Effect of Adult Sex Ratio on Mule Deer and Elk Productivity in Colorado

2001 ◽  
Vol 65 (3) ◽  
pp. 543 ◽  
Author(s):  
Gary C. White ◽  
David J. Freddy ◽  
R. Bruce Gill ◽  
John H. Ellenberger
Keyword(s):  
Sex Ratio ◽  
Mule Deer ◽  
Adult Sex Ratio

scholarly journals Recruitment sex ratios in gray-tailed voles (Microtus canicaudus) in response to density, sex ratio, and season

2003 ◽  
Vol 81 (8) ◽  
pp. 1306-1311 ◽  
Author(s):  
Monica L Bond ◽  
Jerry O Wolff ◽  
Sven Krackow
Keyword(s):  
Population Density ◽  
Sex Ratio ◽  
Resource Competition ◽  
Sex Ratios ◽  
Female Offspring ◽  
High Population ◽  
Reproductive Value ◽  
High Population Density ◽  
Adult Sex Ratio ◽  
Sex Ratio Adjustment

We tested predictions associated with three widely used hypotheses for facultative sex-ratio adjustment of vertebrates using eight enclosed populations of gray-tailed voles, Microtus canicaudus. These were (i) the population sex ratio hypothesis, which predicts that recruitment sex ratios should oppose adult sex-ratio skews, (ii) the local resource competition hypothesis, which predicts female-biased recruitment at low adult population density and male-biased recruitment at high population density, and (iii) the first cohort advantage hypothesis, which predicts that recruitment sex ratios should be female biased in the spring and male biased in the autumn. We monitored naturally increasing population densities with approximately equal adult sex ratios through the spring and summer and manipulated adult sex ratios in the autumn and measured subsequent sex ratios of recruits. We did not observe any significant sex-ratio adjustment in response to adult sex ratio or high population density; we did detect an influence of time within the breeding season, with more female offspring observed in the spring and more male offspring observed in the autumn. Significant seasonal increases in recruitment sex ratios indicate the capacity of female gray-tailed voles to manipulate their offspring sex ratios and suggest seasonal variation in the relative reproductive value of male and female offspring to be a regular phenomenon.

scholarly journals Sexually selected females in the monogamous Western Australian seahorse

2006 ◽  
Vol 274 (1609) ◽  
pp. 521-525 ◽  
Author(s):  
Charlotta Kvarnemo ◽  
Glenn I Moore ◽  
Adam G Jones
Keyword(s):  
Sexual Selection ◽  
Sex Ratio ◽  
Mating System ◽  
Genetic Study ◽  
Mating Success ◽  
Male Preference ◽  
Monogamous Species ◽  
Adult Sex Ratio ◽  
Western Australian ◽  
Selection Differentials

Studies of sexual selection in monogamous species have hitherto focused on sexual selection among males. Here, we provide empirical documentation that sexual selection can also act strongly on females in a natural population with a monogamous mating system. In our field-based genetic study of the monogamous Western Australian seahorse, Hippocampus subelongatus , sexual selection differentials and gradients show that females are under stronger sexual selection than males: mated females are larger than unmated ones, whereas mated and unmated males do not differ in size. In addition, the opportunity for sexual selection (variance in mating success divided by its mean squared) for females is almost three times that for males. These results, which seem to be generated by a combination of a male preference for larger females and a female-biased adult sex ratio, indicate that substantial sexual selection on females is a potentially important but under-appreciated evolutionary phenomenon in monogamous species.

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