Search results for "Sex allocation"
showing 10 items of 28 documents
Sex-allocation conflict and sexual selection throughout the lifespan of eusocial colonies.
2018
AbstractModels of sex allocation conflict are central to evolutionary biology but have mostly assumed static decisions, where resource allocation strategies are constant over colony lifespan. Here, we develop a model to study how the evolution of dynamic resource allocation strategies is affected by the queen-worker conflict in annual eusocial insects. We demonstrate that the time of dispersal of sexuals affects the sex allocation ratio through sexual selection on males. Furthermore, our model provides three predictions that depart from established results of classic static allocation models. First, we find that the queen wins the sex allocation conflict, while the workers determine the max…
Not all sex ratios are equal : the Fisher condition, parental care and sexual selection
2017
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 …
Resource availability and goshawk offspring sex ratio variation: a large-scale ecological phenomenon
2002
Summary 1. Local population studies have shown that sex allocation among many birds and mammals seems to be partly non-random and in connection to surrounding factors, such as environmental or parental quality. In this scenario, if environmental quality varies in space and time, it is feasible that environmental quality also comes to influence offspring sex ratio on larger geographical scales. 2. Investigating this idea - using nation-wide data sets on size-dimorphic Finnish northern goshawks Accipiter gentilis from 1989 to 1998 - we found that offspring sex ratio is related to spatial and temporal variation in availability of their main prey, woodland grouse species. 3. In a majority of lo…
Maternal investment in relation to sex ratio and offspring number in a small mammal - a case for Trivers and Willard theory?
2009
Summary 1. Optimal parental sex allocation depends on the balance between the costs of investing into sons vs. daughters and the benefits calculated as fitness returns. The outcome of this equation varies with the life history of the species, as well as the state of the individual and the quality of the environment. 2. We studied maternal allocation and subsequent fecundity costs of bank voles, Myodes glareolus, by manipulating both the postnatal sex ratio (all-male ⁄ all-female litters) and the quality of rearing environment (through manipulation of litter size by )2 ⁄ +2 pups) of their offspring in a laboratory setting. 3. We found that mothers clearly biased their allocation to female ra…
Sex-ratio and male sexual characters in a population of Blue tits Parus caeruleus
2005
Sex allocation theory proposes that parents should bias the sex ratio of their offspring if the reproductive value of one sex is greater than that of the other. In the monogamous blue tit (Parus caeruleus), males have a greater variance in reproductive success than females, and high-quality males have higher reproductive success than high-quality females due to extrapair paternity. Consequently, females mating with attractive males are expected to produce broods biased toward sons, as sons benefit more than daughters from inheriting their father’s characteristics. Song and plumage color in birds are secondary sexual characters indicating male quality and involved in female choice. We used t…
The evolutionary dynamics of adaptive virginity, sex-allocation, and altruistic helping in haplodiploid animals
2017
In haplodiploids, females can produce sons from unfertilized eggs without mating. However, virgin reproduction is usually considered to be a result of a failure to mate, rather than an adaptation. Here, we build an analytical model for evolution of virgin reproduction, sex-allocation, and altruistic female helping in haplodiploid taxa. We show that when mating is costly (e.g., when mating increases predation risk), virginity can evolve as an adaptive female reproductive strategy. Furthermore, adaptive virginity results in strongly divergent sex-ratios in mated and virgin queen nests ("split sex ratios"), which promotes the evolution of altruistic helping by daughters in mated queen nests. H…
The cavity-nest ant
2014
Colonies of the ant Temnothorax crassispinus inhabit mostly cavities in wood and hollow acorns. Typically in the field, nest sites that can be used by the ant are a limited resource. In a field experiment, it was investigated whether the ants prefer a specific size of nest, when different ones are available. In July 2011, a total of 160 artificial nests were placed in a beech-pine forest. Four artificial nests (pieces of wood with volume cavities, ca 415, 605, 730, and 980 mm3, respectively) were located on each square meter of the experimental plot. One year later, shortly before the emergence of new sexuals, the nests were collected. In July 2012, colonies inhabited more frequently bigger…
Paternal effects on functional gender account for cryptic dioecy in a perennial plant.
2004
7 páginas, 3 figuras, 1 tabla.
Sex Allocation in Haplodiploid Cyclical Parthenogens with Density‐Dependent Proportion of Males
1998
Departament de Microbiologia i Ecologia, Universitat de Birky and Gilbert 1971; Wallace and Snell 1991), which Valencia, E46100-Burjassot (Valencia), Spain includes an asexual (amictic) and a sexual (mictic) phase, the diapausing form being the sexually produced resting Submitted September 22, 1997; Accepted April 21, 1998 egg. Habitat colonization begins when the resting eggs hatch and emerge from the sediments. With these hatchlings, the amictic phase starts, which is a repeated sequence of amictic females parthenogenetically produc
A trade-off between current and future sex allocation revealed by maternal energy budget in a small mammal.
2011
Sex-allocation theories generally assume differential fitness costs of raising sons and daughters. Yet, experimental confirmation of such costs is scarce and potential mechanisms are rarely addressed. While the most universal measure of physiological costs is energy expenditure, only one study has related the maternal energy budget to experimentally controlled offspring sex. Here, we experimentally test this in the bank vole (Myodes glareolus) by simultaneously manipulating the litter's size and sex ratio immediately after birth. Two weeks after manipulation, when mothers were at the peak of lactation and were pregnant with concurrent litters, we assessed their energy budget. We found that …