Search results for "Semelparity and iteroparity"
showing 10 items of 10 documents
Throwing down a genomic gauntlet on fisheries-induced evolution
2021
Beginning with studies on crypsis and camouflage, the hypothesis that predators can generate evolutionary change in their prey has a long and rich history (1). Few predators, however, rival humans in their potential to generate selection responses and concomitant phenotypic change on contemporary timescales. In the 1930s, J. B. S. Haldane (2) mused that fishing would be an ideal candidate for such “observable evolution” within a human lifetime, proceeding “with extreme and abnormal speed.” However, it was not until the late 1970s that research on fisheries-induced evolution (FIE) gained a substantive scientific foothold, beginning with thought-provoking work on Canadian whitefish ( Coregonu…
Evolutionary population dynamics
2005
The interface between the evolution of life history traits and population dynamics in temporally and spatially variable environments is the topic of this chapter. Thus, the frame for the life history processes is set by spatial and temporal fluctuations in population density. Here, we will focus primarily on modes of reproduction and we are especially interested in whether alternative reproductive strategies can co-exist in a population. We show that spatially structured populations may allow co-existence of various life history strategies that do not easily co-exist in a nonstructured environment. Also, intrinsic and external temporal fluctuations in the environment tend to enhance polymor…
Does evolution of iteroparous and semelparous reproduction call for spatially structured systems?
2000
A persistent question in the evolution of life histories is the fitness trade-off between reproducing only once (semelparity) in a lifetime or reproducing repeated times in different seasons (iteroparity). The problem can be formulated into a research agenda by assuming that one reproductive strategy is resident (has already evolved) and by asking whether invasion (evolution) of an alternative reproductive strategy is possible. For a spatially nonstructured system, Bulmer (1994) derived the relationship v + PA1 (PA is adult survival; vbS and bS are offspring numbers for iteroparous and semelparous breeding strategies, respectively) at which semelparous population cannot be invaded by an ite…
Environmental Variability and Semelparity vs. Iteroparity as Life Histories
2002
Research on the evolution of life histories addresses the topic of fitness trade-offs between semelparity (reproducing once in a lifetime) and iteroparity (repeated reproductive bouts per lifetime). Bulmer (1994) derived the relationship v+P(A)<1 (P(A) is the adult survival;vb(S) and b(S) are the offspring numbers for iteroparous and semelparous breeding strategies, respectively), under which a resident semelparous population cannot be invaded by an iteroparous mutant when the underlying population dynamics are stable. We took Bulmer's population dynamics, and added noise in juvenile and adult survival and in offspring numbers. Long-term coexistence of the two strategies is possible in much…
Predation risk and reproduction in the bank vole
2012
Context Life-history strategies are the means that organisms use to achieve successful reproduction in environments that vary in time and space. Individual animals maximise life-time reproductive success (LRS) through optimal timing of reproduction and investment in offspring. A crucial factor affecting LRS is predation risk in a highly seasonal environment. According to the breeding-suppression hypothesis (BSH), females should delay breeding under short periods of high predation risk. Delayed breeding under risk is suggested to have substantial consequences for females’ fitness. Aims We tested the BSH in an iteroparous boreal small rodent, the bank vole, Myodes glareolus. Methods We used …
Is the impact of environmental noise visible in the dynamics of age-structured populations?
2001
Climate change has ignited lively research into its impact on various population–level processes. The research agenda in ecology says that some of the fluctuations in population size are accountable for by the external noise (e.g. weather) modulating the dynamics of populations. We obeyed the agenda by assuming population growth after a resource–limited Leslie matrix model in an age–structured population. The renewal process was disturbed by superimposing noise on the development of numbers in one or several age groups. We constructed models for iteroparous and semelparous breeders so that, for both categories, the population growth rate was matching. We analysed how the modulated populatio…
Is reproduction really costly? Energy metabolism of bank vole (Clethrionomys glareolus) females through the reproductive cycle
2007
Energetic requirements during reproduction are important determinants of the onset of reproduction and of breeding strategy (e.g., breeding post-partum) and therefore affect female reproductive output in seasonally varying environments. To balance the energetic needs of breeding with energy availability, females must optimize energy allocation between their own energy use and energy allocated to their litter. Here, we studied energetic costs and potential energetic trade-offs of reproduction in female bank voles (Clethrionomys glareolus). We measured energy consumption, i.e., metabolic rates as determined from carbon dioxide production of females either with their pups (breeding unit) to fi…
Beyond lifetime reproductive success: the posthumous reproductive dynamics of male Trinidadian guppies
2013
In semelparous populations, dormant germ banks (e.g. seeds) have been proposed as important in maintaining genotypes that are adaptive at different times in fluctuating environments. Such hidden storage of genetic diversity need not be exclusive to dormant banks. Genotype diversity may be preserved in many iteroparous animals through sperm-storage mechanisms in females. This allows males to reproduce posthumously and increase the effective sizes of seemingly female-biased populations. Although long-term sperm storage has been demonstrated in many organisms, the understanding of its importance in the wild is very poor. We here show the prevalence of male posthumous reproduction in wild Trini…
Sexual and reproductive traits of Hypania invalida (Polychaeta, Ampharetidae): a remarkable invasive species in Central European waterways
2010
SUMMARY 1. The Ponto-Caspian polychaete Hypania invalida (Archiv fur Naturgeschichte, 1860, 26, 109) is undergoing rapid range expansion in the Rhine and other central European waterways. We examined its reproductive traits in an attempt to account for its remarkable invasive success. 2. For the first time in this species, we found males, dioecy (gonochorism) and an exclusively sexual mode of reproduction; no indication for hermaphroditism or (unisexual) partheno- genesis, that could explain the rapid range expansion of H. invalida, was found. 3. Our experimental evidence shows that H. invalida reproduces by males discharging their sperm into the water column while eggs are retained and fer…
Phenotypic tradeoffs between egg number and egg size in three parasitic anisakid nematodes
2007
Phenotypic tradeoffs between number and size of eggs were tested in three component populations of three marine anisakid nematodes: Anisakis simplex, Pseudoterranova decipiens and Contracaecum osculatum. Body and uterine volumes (as proxies of female size), and egg number, mean egg volume and clutch volume (as descriptors of reproductive output) were measured in 50 females of each species. Evidence of a phenotypic tradeoff was detected only in A. simplex; the first time that has been found in a parasite population. Comparison of feasible values inferred from the van Noordwijk and de Jong's model and current data showed that interindividual variation in egg size was narrower than expected in…