scholarly journals SEXUAL SELECTION CAN INCREASE THE EFFECT OF RANDOM GENETIC DRIFT-A QUANTITATIVE GENETIC MODEL OF POLYMORPHISM IN OOPHAGA PUMILIO, THE STRAWBERRY POISON-DART FROG

Evolution ◽  
2009 ◽  
Vol 64 (6) ◽  
pp. 1719-1728 ◽  
Author(s):  
Samuel J. Tazzyman ◽  
Yoh Iwasa
2019 ◽  
Vol 116 (46) ◽  
pp. 23225-23231 ◽  
Author(s):  
Maria R. Servedio ◽  
John M. Powers ◽  
Russell Lande ◽  
Trevor D. Price

In many species that form pair bonds, males display to their mate after pair formation. These displays elevate the female’s investment into the brood. This is a form of cooperation because without the display, female investment is reduced to levels that are suboptimal for both sexes. The presence of such displays is paradoxical as in their absence the male should be able to invest extra resources directly into offspring, to the benefit of both sexes. We consider that the origin of these displays lies in the exploitation of preexisting perceptual biases which increase female investment beyond that which is optimal for her, initially resulting in a sexual conflict. We use a combined population genetic and quantitative genetic model to show how this conflict becomes resolved into sexual cooperation. A cooperative outcome is most likely when perceptual biases are under selection pressures in other contexts (e.g., detection of predators, prey, or conspecifics), but this is not required. Cooperation between pair members can regularly evolve even when this provides no net advantage to the pair and when the display itself reduces a male’s contributions to raising the brood. The findings account for many interactions between the sexes that have been difficult to explain in the context of sexual selection.


2005 ◽  
Vol 20 (1) ◽  
pp. 5-14 ◽  
Author(s):  
L.R. DeHaan ◽  
D.L. Van Tassel ◽  
T.S. Cox

AbstractPerennial grain crops would address many agricultural problems, including soil erosion, nutrient loss and pesticide contamination. Doubts about the possibility of perennial grain crops rest upon two assumptions: (1) that the relationship between yield and longevity is a fixed function that cannot be influenced by selection, mutation or environmental changes; and (2) that yield and longevity trade off in a bivariate manner to the exclusion of all other traits. These assumptions are consistent with the phenotypic trade-off model, but recent research suggests that a quantitative genetic model is a more appropriate approach to trade-offs. In the quantitative genetic model, environmental and genetic changes can result in increases in two traits simultaneously even when a trade-off, or negative correlation, exists between the two traits. Empirical evidence that the trade-off between perenniality and reproductive allocation is not fixed comes from wild, herbaceous perennials that can produce more than 2000 kg seed ha−1 in the temperate zone, and herbaceous perennial crops that produce on average 8900 kg fruit ha−1 in the tropics. Ecological literature suggests that most perennials produce small amounts of seed relative to their vegetative growth not as a physiological absolute, but rather as a result of natural selection in a stable, competitive environment favoring longevity. By selecting strongly for seed yield in a population of perennial plants, the plant breeder can likely achieve that which is rare in nature—a high seed-yielding perennial plant. The same general methodologies that have allowed annual grain breeders to increase grain yield and push many combinations of negatively correlated traits to levels of expression not seen in nature are available to the perennial grain breeder. Perennial grain breeders are integrating ecological principles and traditional plant breeding methods in their efforts to develop perennial grain wheat (Triticum spp.), sorghum (Sorghum spp.), sunflower (Helianthus spp.), Illinois bundleflower (Desmanthus illinoensis) and rice (Oryza spp.).


2007 ◽  
Vol 8 (5) ◽  
pp. 343-350 ◽  
Author(s):  
Song Wu ◽  
Jie Yang ◽  
Chenguang Wang ◽  
Rongling Wu

Genome ◽  
1989 ◽  
Vol 31 (1) ◽  
pp. 221-227 ◽  
Author(s):  
Russell Lande

Fisher's theory of sexual selection, Wright's shifting-balance theory, and recent models based on them are reviewed as mechanisms of animal speciation. The joint evolution of mating preferences and secondary sexual characters can cause rapid nonadaptive phenotypic divergence and premating isolation between geographically separated populations, or along a cline. Extensive comparative data on Drosophila species support the suggestion of R. A. Fisher and T. Dobzhansky that the evolution of mating preferences can reinforce partial postmating isolation between sympatric populations. The interaction of natural selection and random genetic drift in local populations with a small effective size can produce a rapid transition between relatively stable phenotypes separated by an adaptive valley, or between chromosomal rearrangements with a heterozygote disadvantage. Large demographic fluctuations, such as frequent random local extinction and colonization, are required for the rapid spread of new adaptations (or karyotypes) when intermediate phenotypes (or rearrangement heterozygotes) are selected against.Key words: reproductive isolation, hybridization, sexual selection, reinforcement, subdivided population, shifting balance, adaptive landscape, random genetic drift.


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