Life History Evolution in Guppies: III. The Impact of Prawn Predation on Guppy Life Histories

Oikos ◽  
1991 ◽  
Vol 62 (1) ◽  
pp. 13 ◽  
Author(s):  
F. Helen Rodd ◽  
David N. Reznick
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Evolution ◽  
History Evolution ◽  
The Impact

The evolution of childhood as a by-product?

2006 ◽  
Vol 29 (3) ◽  
pp. 288-289
Author(s):  
Peter Kappeler
Keyword(s):  
Life History ◽  
Life Histories ◽  
Nonhuman Primates ◽  
Homo Sapiens ◽  
Human Life ◽  
Life History Evolution ◽  
History Evolution ◽  
Linguistic Skills

The proposition that selective advantages of linguistic skills have contributed to shifts in ontogenetic landmarks of human life histories in early Homo sapiens is weakened by neglecting alternative mechanisms of life history evolution. Moreover, arguments about biological continuity through sweeping comparisons with nonhuman primates do not support various assumptions of this scenario.

scholarly journals From stochastic environments to life histories and back

2009 ◽  
Vol 364 (1523) ◽  
pp. 1499-1509 ◽  
Author(s):  
Shripad Tuljapurkar ◽  
Jean-Michel Gaillard ◽  
Tim Coulson
Keyword(s):  
Life History ◽  
Growth Rates ◽  
Life Histories ◽  
Life History Evolution ◽  
Environmental Stochasticity ◽  
Vital Rates ◽  
Stochastic Growth ◽  
Individual Fitness ◽  
History Evolution ◽  
Average Individual

Environmental stochasticity is known to play an important role in life-history evolution, but most general theory assumes a constant environment. In this paper, we examine life-history evolution in a variable environment, by decomposing average individual fitness (measured by the long-run stochastic growth rate) into contributions from average vital rates and their temporal variation. We examine how generation time, demographic dispersion (measured by the dispersion of reproductive events across the lifespan), demographic resilience (measured by damping time), within-year variances in vital rates, within-year correlations between vital rates and between-year correlations in vital rates combine to determine average individual fitness of stylized life histories. In a fluctuating environment, we show that there is often a range of cohort generation times at which the fitness is at a maximum. Thus, we expect ‘optimal’ phenotypes in fluctuating environments to differ from optimal phenotypes in constant environments. We show that stochastic growth rates are strongly affected by demographic dispersion, even when deterministic growth rates are not, and that demographic dispersion also determines the response of life-history-specific average fitness to within- and between-year correlations. Serial correlations can have a strong effect on fitness, and, depending on the structure of the life history, may act to increase or decrease fitness. The approach we outline takes a useful first step in developing general life-history theory for non-constant environments.

scholarly journals Unrestricted migration favours virulent pathogens in experimental metapopulations: evolutionary genetics of a rapacious life history

2010 ◽  
Vol 365 (1552) ◽  
pp. 2503-2513 ◽  
Author(s):  
Christal M. Eshelman ◽  
Roxanne Vouk ◽  
Jodi L. Stewart ◽  
Elizabeth Halsne ◽  
Haley A. Lindsey ◽  
...  
Keyword(s):  
Population Structure ◽  
Life History ◽  
Negative Relationship ◽  
Life History Evolution ◽  
Tragedy Of The Commons ◽  
Viral Pathogen ◽  
Lower Productivity ◽  
The Commons ◽  
History Evolution ◽  
The Impact

Understanding pathogen infectivity and virulence requires combining insights from epidemiology, ecology, evolution and genetics. Although theoretical work in these fields has identified population structure as important for pathogen life-history evolution, experimental tests are scarce. Here, we explore the impact of population structure on life-history evolution in phage T4, a viral pathogen of Escherichia coli . The host–pathogen system is propagated as a metapopulation in which migration between subpopulations is either spatially restricted or unrestricted. Restricted migration favours pathogens with low infectivity and low virulence. Unrestricted migration favours pathogens that enter and exit their hosts quickly, although they are less productive owing to rapid extirpation of the host population. The rise of such ‘rapacious’ phage produces a ‘tragedy of the commons’, in which better competitors lower productivity. We have now identified a genetic basis for a rapacious life history. Mutations at a single locus ( rI ) cause increased virulence and are sufficient to account for a negative relationship between phage competitive ability and productivity. A higher frequency of rI mutants under unrestricted migration signifies the evolution of rapaciousness in this treatment. Conversely, spatially restricted migration favours a more ‘prudent’ pathogen strategy, in which the tragedy of the commons is averted. As our results illustrate, profound epidemiological and ecological consequences of life-history evolution in a pathogen can have a simple genetic cause.

scholarly journals Predation and Resource Availability Interact to Drive Life-History Evolution in an Adaptive Radiation of Livebearing Fish

2021 ◽  
Vol 9 ◽  
Author(s):  
Kaj Hulthén ◽  
Jacob S. Hill ◽  
Matthew R. Jenkins ◽  
Randall Brian Langerhans
Keyword(s):  
Life History ◽  
Predation Risk ◽  
Resource Availability ◽  
Life Histories ◽  
A Priori ◽  
Life History Evolution ◽  
Selective Agents ◽  
Two Factors ◽  
High Predation ◽  
History Evolution

Predation risk and resource availability are two primary factors predicted by theory to drive the evolution of life histories. Yet, disentangling their roles in life-history evolution in the wild is challenging because (1) the two factors often co-vary across environments, and (2) environmental effects on phenotypes can mask patterns of genotypic evolution. Here, we use the model system of the post-Pleistocene radiation of Bahamas mosquitofish (Gambusia hubbsi) inhabiting blue holes to provide a strong test of the roles of predation and resources in life-history evolution, as the two factors do not co-vary in this system and we attempted to minimize environmental effects by raising eight populations under common laboratory conditions. We tested a priori predictions of predation- and resource-driven evolution in five life-history traits. We found that life-history evolution in Bahamas mosquitofish largely reflected complex interactions in the effects of predation and resource availability. High predation risk has driven the evolution of higher fecundity, smaller offspring size, more frequent reproduction, and slower growth rate—but this predation-driven divergence primarily occurred in environments with relatively high resource availability, and the effects of resources on life-history evolution was generally greater within environments having high predation risk. This implies that resource-driven selection on life histories overrides selection from predators when resources are particularly scarce. While several results matched a priori predictions, with the added nuance of interdependence among selective agents, some did not. For instance, only resource levels, not predation risk, explained evolutionary change in male age at maturity, with more rapid sexual maturation in higher-resource environments. We also found faster (not slower) juvenile growth rates within low-resource and low-predation environments, probably caused by selection in these high-competition scenarios favoring greater growth efficiency. Our approach, using common-garden experiments with a natural system of low- and high-predation populations that span a continuum of resource availability, provides a powerful way to deepen our understanding of life-history evolution. Overall, it appears that life-history evolution in this adaptive radiation has resulted from a complex interplay between predation and resources, underscoring the need for increased attention on more sophisticated interactions among selective agents in driving phenotypic diversification.

Ecophysiological responses in life-history evolution: evidence for their importance in a geographically widespread insect species complex

1986 ◽  
Vol 64 (4) ◽  
pp. 875-884 ◽  
Author(s):  
Catherine A. Tauber ◽  
Maurice J. Tauber
Keyword(s):  
Life History ◽  
Genetic Variability ◽  
Life Histories ◽  
Life History Evolution ◽  
Physiological Basis ◽  
Geographical Patterns ◽  
Species Complexes ◽  
Evolution Of Life ◽  
Ecophysiological Responses ◽  
History Evolution

Geographical patterns of variation among North American populations of Chrysoperla carnea provide strong evidence that ecophysiological traits are central to the evolution of life histories. Selection pressure and the types and amounts of genetic variability underlying the traits vary geographically. Western populations exhibit considerable genetic variability in their reproductive responses to both photoperiod and prey. This variability is expressed both at the interpopulation level by the diversity of locally adapted populations and at the intrapopulation level in the form of genetic polymorphisms. By contrast, eastern, midwestern, and northwestern regions contain two types of reproductively isolated, monomorphic populations. The two types differ in their photoperiodic requirements for reproduction, but neither uses prey as a cue to stimulate reproduction. Although most of the characteristic responses to photoperiod and prey can vary independently of each other, the separate traits tend to covary to form coadaptive sets. The covariance of a few responses appears to have a genetic or physiological basis, a condition that places constraints on the evolution of life histories. Our results also demonstrate that comparative studies at the intraspecific level are highly significant to the analysis of life-history evolution and to the taxonomic treatment of species complexes.

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