期刊论文详细信息
BMC Evolutionary Biology
Exploring power and parameter estimation of the BiSSE method for analyzing species diversification
Wayne Maddison2  Peter E Midford1  Matthew P Davis3 
[1] NESCent: National Evolutionary Synthesis Center, 2024 W. Main Street, Suite A200, Durham, NC, 27705-4667, USA;University of British Columbia, 4200-6270 University Blvd, Vancouver, B.C, Canada, V6T 1Z4;The Field Museum, 1400 South Lake Shore Drive, Chicago, IL, 60605, USA
关键词: Systematics;    Character evolution;    Key innovations;   
Others  :  1129938
DOI  :  10.1186/1471-2148-13-38
 received in 2012-09-14, accepted in 2013-01-24,  发布年份 2013
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【 摘 要 】

Background

There has been a considerable increase in studies investigating rates of diversification and character evolution, with one of the promising techniques being the BiSSE method (binary state speciation and extinction). This study uses simulations under a variety of different sample sizes (number of tips) and asymmetries of rate (speciation, extinction, character change) to determine BiSSE’s ability to test hypotheses, and investigate whether the method is susceptible to confounding effects.

Results

We found that the power of the BiSSE method is severely affected by both sample size and high tip ratio bias (one character state dominates among observed tips). Sample size and high tip ratio bias also reduced accuracy and precision of parameter estimation, and resulted in the inability to infer which rate asymmetry caused the excess of a character state. In low tip ratio bias scenarios with appropriate tip sample size, BiSSE accurately estimated the rate asymmetry causing character state excess, avoiding the issue of confounding effects.

Conclusions

Based on our findings, we recommend that future studies utilizing BiSSE that have fewer than 300 terminals and/or have datasets where high tip ratio bias is observed (i.e., fewer than 10% of species are of one character state) should be extremely cautious with the interpretation of hypothesis testing results.

【 授权许可】

   
2013 Davis et al; licensee BioMed Central Ltd.

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