Spatially explicit neutral models for population genetics and community ecology: Extensions of the Neyman–Scott clustering process

2010 ◽  
Vol 77 (1) ◽  
pp. 32-41 ◽  
Author(s):  
Ichiro K. Shimatani
2016 ◽  
Vol 113 (29) ◽  
pp. 8079-8086 ◽  
Author(s):  
Leslie J. Rissler

Phylogeography and landscape genetics have arisen within the past 30 y. Phylogeography is said to be the bridge between population genetics and systematics, and landscape genetics the bridge between landscape ecology and population genetics. Both fields can be considered as simply the amalgamation of classic biogeography with genetics and genomics; however, they differ in the temporal, spatial, and organismal scales addressed and the methodology used. I begin by briefly summarizing the history and purview of each field and suggest that, even though landscape genetics is a younger field (coined in 2003) than phylogeography (coined in 1987), early studies by Dobzhansky on the “microgeographic races” of Linanthus parryae in the Mojave Desert of California and Drosophila pseudoobscura across the western United States presaged the fields by over 40 y. Recent advances in theory, models, and methods have allowed researchers to better synthesize ecological and evolutionary processes in their quest to answer some of the most basic questions in biology. I highlight a few of these novel studies and emphasize three major areas ripe for investigation using spatially explicit genomic-scale data: the biogeography of speciation, lineage divergence and species delimitation, and understanding adaptation through time and space. Examples of areas in need of study are highlighted, and I end by advocating a union of phylogeography and landscape genetics under the more general field: biogeography.


Genetics ◽  
1985 ◽  
Vol 109 (4) ◽  
pp. 799-812
Author(s):  
Alan Hastings

ABSTRACT Using perturbation techniques, I determine the equilibrium of two-locus two-allele models with overdominance and weak epistasis. To lowest order, the allele frequencies, the mean fitness and the covariance between heterokaryotic and homokaryotic flies arising in the Sturtevant experimental design are independent of the recombination rate, r. The disequilibrium varies as one divided by the recombination rate, in contrast to neutral models. Although the disequilibrium generated by weak epistasis is small, too small to be experimentally detected, it can be large enough to have biological importance.


ÈKOBIOTEH ◽  
2020 ◽  
Vol 3 (3) ◽  
pp. 472-477
Author(s):  
G.S. Rozenberg ◽  

Community ecology studies the patterns of changes in biodiversity, species structure, and the number of individual populations in a spatial and temporal aspect. The article discusses some modern theories of community ecology (neutral theory, patch dynamics, M. Vellend's ideas about four basic processes in communities similar to processes of population genetics [selection, drift, dispersal, selection], etc.).


2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Pablo A. Marquet ◽  
Guillermo Espinoza ◽  
Sebastian R. Abades ◽  
Angela Ganz ◽  
Rolando Rebolledo

Genetics ◽  
1979 ◽  
Vol 92 (4) ◽  
pp. 1329-1345
Author(s):  
L J Lester ◽  
R K Selander

ABSTRACT Genic variation of seven species of Hymenoptera is described, using electrophoretic techniques. The heterozygosities range from 0.033 to 0.084. An average heterozygosity is calculated for 23 species of haplodiploid insects, and this value is significantly different from the same value for 18 Drosophila species or for W diploid insect species (including Drosophila). The niche width-gepetic variation hypothesis is rejected as an explanation. A comparison of selection models and neutral models shows that both hypotheses are capable of explaining the data.


Author(s):  
Nicholas M. Sard ◽  
Robert D. Hunter ◽  
Edward F. Roseman ◽  
Daniel B. Hayes ◽  
Robin L. DeBruyne ◽  
...  

2020 ◽  
Vol 11 (10) ◽  
pp. 1237-1246
Author(s):  
Samuel E. D. Thompson ◽  
Ryan A. Chisholm ◽  
James Rosindell

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