The number of markers and samples needed for detecting bottlenecks under realistic scenarios, with and without recovery: a simulation-based study

被引:61
作者
Hoban, Sean M. [1 ]
Gaggiotti, Oscar E. [2 ]
Bertorelle, Giorgio [1 ]
机构
[1] Univ Ferrara, Dipartimento Sci Vita & Biotecnol, I-44100 Ferrara, Italy
[2] Univ Grenoble 1, Lab Ecol Alpine, F-38041 Grenoble, France
关键词
conservation; genomic; heterozygote excess; M-ratio; power; recovery; GENETIC DIVERSITY; STATISTICAL-METHODS; POPULATION; CONSERVATION; POWER; SIZE; CONSEQUENCES; PROGRAM; HISTORY; TESTS;
D O I
10.1111/mec.12258
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Detecting bottlenecks is a common task in molecular ecology. While several bottleneck detection methods exist, evaluations of their power have focused only on severe bottlenecks (e.g. to Ne similar to 10). As a component of a recent review, Peery etal. () analysed the power of two approaches, the M-ratio and heterozygote excess tests, to detect moderate bottlenecks (e.g. to Ne similar to 100), which is realistic for many conservation situations. In this Comment, we address three important points relevant to but not considered in Peery etal. Under moderate bottleneck scenarios, we test the (i) relative advantage of sampling more markers vs. more individuals, (ii) potential power to detect the bottleneck when utilizing dozens of microsatellites (a realistic possibility for contemporary studies) and (iii) reduction in power when postbottleneck recovery has occurred. For the realistic situations examined, we show that (i) doubling the number of loci shows equal or better power than tripling the number of individuals, (ii) increasing the number of markers (up to 100) results in continued additive gains in power, and (iii) recovery after a moderate amount of time or gradual change in size reduces power, by up to one-half. Our results provide a practical supplement to Peery etal. and encourage the continued use of bottleneck detection methods in the genomic age, but also emphasize that the power under different sampling schemes should be estimated, using simulation modelling, as a routine component of molecular ecology studies.
引用
收藏
页码:3444 / 3450
页数:7
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