Biomedical subjects

R Härdling

Publications and source records attributed to R Härdling.

4 recordsLinked to original sources

PubMed2005

The evolution of repeated mating under sexual conflict.

In insects, repeated mating by females may have direct effects on female fecundity, fertility, and longevity. In addition, a female's remating rate affects her fitness through mortality costs of male harassment and ecological risks of mating such as predation. We analyse a model where these female fitness factors are put into their life-history context, and traded against each other, while accounting for limitations because of mate availability. We solve analytically for the condition when female multiple mating will evolve. We show that the probability that a female mates with a courting male decreases with increases in population density. The extent of conflict between the sexes thus automatically becomes larger at higher densities. However, because at higher densities females meet males at a higher rate, the resulting ESS female remating rate is independent of population density. The female remating probability is in conflict with male adaptations that increase male mating rate by persuading or forcing females to mate, and also in conflict with male adaptations for protecting the own sperm from being removed by future female mates. We show that the relative importance of these conflicts depends on population density.

Animals↗

PubMed2000

Clutch size evolution under sexual conflict enhances the stability of mating systems.

Models of optimal clutch size often implicitly assume a situation with uniparental care. However, the evolutionary conflict between males and females over the division of parental care will have a major influence on the evolution of clutch size. Since clutch size is a female trait, a male has little possibility of directly influencing it. However, the optimal clutch size from a female's perspective will depend on the amount of paternal care her mate is expected to provide. The sexual conflict over parental care will in its turn be affected by clutch size, since a larger clutch makes male care more valuable. Hence, there will be joint evolution of mating system and clutch size. In this paper, we demonstrate that this joint evolution will tend to stabilize the mating system. In a situation with conventional sex roles, this joint evolution might result in either increased clutch size and biparental care or reduced clutch size and uniparental female care. Under some circumstances the initial conditions might determine which will be the outcome. These results demonstrate that it may be difficult to deduce whether biparental care evolved because of few opportunities for breeding males increasing their fitness by attracting additional mates or because of the importance of male care for offspring fitness by studying prevailing mating systems using, for example, male removals or manipulation of males' opportunities for finding additional mates. In general terms, we demonstrate that models of life-history evolution have to consider the social context in which they evolve.

Animals↗

PubMed2000

Dynamics of intersexual conflict over precopulatory mate guarding in two populations of the isopod Idotea baltica.

Aggressiveness during intersexual conflicts is predicted to depend on its costs, the value of winning and the power asymmetry of the contestants, all of which may vary between populations. In the marine isopod Idotea baltica (Pallas) a conflict occurs as females resist the attempts by males to start precopulatory mate guarding. We analysed contest dynamics with respect to female maturity stage, that is, to time left to reproductive moult, with which the payoffs of guarding for males and females change. We did this in two populations that differ in synchrony of reproduction, sex ratio and the degree of sexual dimorphism. The intensity and dynamics of contests differed between populations: in the more size-dimorphic population, females, the smaller sex, resisted less by forceful flexing but more by hooking their body than in the other population. Male aggressiveness stayed at a constant level with respect to female maturity. In the less size-dimorphic population, female resistance by flexing was intense and it decreased, while male persistence increased, with the approaching reproductive moult. Contests were more intense with small than with large males. These results fit well with the predictions from models of conflict behaviour. Assessment of the payoffs of winning versus contest costs, coadaptation of the level of aggressiveness to the other traits affecting contest outcome, and counteradaptations by the sexes to each other largely explain the dynamics and between-population differences of these contests. Copyright 2000 The Association for the Study of Animal Behaviour.

Journal Article↗

PubMed1999

Arms Races, Conflict Costs and Evolutionary Dynamics.

In conflicts and fights, the winner is often determined by the difference in resource-holding potential, e.g. size, weaponry, strength (RHP). I model the evolution of RHP in a symmetric game with continuous strategies. I show that there is a convergence stable ESS level of RHP if the cost of the trait increases faster than linearly, and that this is the only solution if the cost increases fast enough with RHP. Otherwise with slowly increasing cost, the solution is a cyclically fluctuating level of RHP. It is also shown that if the cost increases linearly with RHP, the only solution to the game is neutrally stable cycles, the amplitude determined by the initial conditions. The cycles come about because in a population drawn into an arms race of RHP, individuals after a while suffer costs so high that mutants with the lowest possible armament level may invade. Copyright 1999 Academic Press.

Journal Article↗