Population size, plant performance, and genetic variation in the rare plant Arnica montana L. in the Rhön, Germany

2000 ◽  
Vol 1 (1) ◽  
pp. 43-51 ◽  
Author(s):  
Stefanie Kahmen ◽  
Peter Poschlod
2000 ◽  
Vol 14 (6) ◽  
pp. 1776-1787 ◽  
Author(s):  
Sheila H. Luijten ◽  
Angelo Dierick ◽  
J. Gerard ◽  
B. Oostermeijer ◽  
Leon E. L. Raijmann ◽  
...  

2000 ◽  
Vol 14 (6) ◽  
pp. 1776-1787 ◽  
Author(s):  
Sheila H. Luijten ◽  
Angelo Dierick ◽  
J. Gerard ◽  
B. Oostermeijer ◽  
Léon E. L. Raijmann ◽  
...  

2006 ◽  
Vol 94 (5) ◽  
pp. 942-952 ◽  
Author(s):  
ROOSA LEIMU ◽  
PIA MUTIKAINEN ◽  
JULIA KORICHEVA ◽  
MARKUS FISCHER

2020 ◽  
Author(s):  
Kimberly J. Gilbert ◽  
Stefan Zdraljevic ◽  
Daniel E. Cook ◽  
Asher D. Cutter ◽  
Erik C. Andersen ◽  
...  

ABSTRACTThe distribution of fitness effects for new mutations is one of the most theoretically important but difficult to estimate properties in population genetics. A crucial challenge to inferring the distribution of fitness effects (DFE) from natural genetic variation is the sensitivity of the site frequency spectrum to factors like population size change, population substructure, and non-random mating. Although inference methods aim to control for population size changes, the influence of non-random mating remains incompletely understood, despite being a common feature of many species. We report the distribution of fitness effects estimated from 326 genomes of Caenorhabditis elegans, a nematode roundworm with a high rate of self-fertilization. We evaluate the robustness of DFE inferences using simulated data that mimics the genomic structure and reproductive life history of C. elegans. Our observations demonstrate how the combined influence of self-fertilization, genome structure, and natural selection can conspire to compromise estimates of the DFE from extant polymorphisms. These factors together tend to bias inferences towards weakly deleterious mutations, making it challenging to have full confidence in the inferred DFE of new mutations as deduced from standing genetic variation in species like C. elegans. Improved methods for inferring the distribution of fitness effects are needed to appropriately handle strong linked selection and selfing. These results highlight the importance of understanding the combined effects of processes that can bias our interpretations of evolution in natural populations.


2014 ◽  
Vol 281 (1790) ◽  
pp. 20140370 ◽  
Author(s):  
Dylan J. Fraser ◽  
Paul V. Debes ◽  
Louis Bernatchez ◽  
Jeffrey A. Hutchings

Whether and how habitat fragmentation and population size jointly affect adaptive genetic variation and adaptive population differentiation are largely unexplored. Owing to pronounced genetic drift, small, fragmented populations are thought to exhibit reduced adaptive genetic variation relative to large populations. Yet fragmentation is known to increase variability within and among habitats as population size decreases. Such variability might instead favour the maintenance of adaptive polymorphisms and/or generate more variability in adaptive differentiation at smaller population size. We investigated these alternative hypotheses by analysing coding-gene, single-nucleotide polymorphisms associated with different biological functions in fragmented brook trout populations of variable sizes. Putative adaptive differentiation was greater between small and large populations or among small populations than among large populations. These trends were stronger for genetic population size measures than demographic ones and were present despite pronounced drift in small populations. Our results suggest that fragmentation affects natural selection and that the changes elicited in the adaptive genetic composition and differentiation of fragmented populations vary with population size. By generating more variable evolutionary responses, the alteration of selective pressures during habitat fragmentation may affect future population persistence independently of, and perhaps long before, the effects of demographic and genetic stochasticity are manifest.


Sign in / Sign up

Export Citation Format

Share Document