Nested radiations and the pulse of angiosperm diversification: increased diversification rates often follow whole genome duplications

  • David C. Tank
    Department of Biological Sciences University of Idaho Moscow ID 83844 USA
  • Jonathan M. Eastman
    Department of Biological Sciences University of Idaho Moscow ID 83844 USA
  • Matthew W. Pennell
    Department of Biological Sciences University of Idaho Moscow ID 83844 USA
  • Pamela S. Soltis
    Florida Museum of Natural History University of Florida Gainesville FL 32611 USA
  • Douglas E. Soltis
    Florida Museum of Natural History University of Florida Gainesville FL 32611 USA
  • Cody E. Hinchliff
    Department of Ecology and Evolutionary Biology University of Michigan Ann Arbor MI 48109 USA
  • Joseph W. Brown
    Department of Ecology and Evolutionary Biology University of Michigan Ann Arbor MI 48109 USA
  • Emily B. Sessa
    Department of Biology University of Florida Gainesville FL 32611 USA
  • Luke J. Harmon
    Department of Biological Sciences University of Idaho Moscow ID 83844 USA

Description

<jats:title>Summary</jats:title><jats:p> <jats:list list-type="bullet"> <jats:list-item><jats:p>Our growing understanding of the plant tree of life provides a novel opportunity to uncover the major drivers of angiosperm diversity.</jats:p></jats:list-item> <jats:list-item><jats:p>Using a time‐calibrated phylogeny, we characterized hot and cold spots of lineage diversification across the angiosperm tree of life by modeling evolutionary diversification using stepwise AIC (MEDUSA). We also tested the whole‐genome duplication (<jats:styled-content style="fixed-case">WGD</jats:styled-content>) radiation lag‐time model, which postulates that increases in diversification tend to lag behind established <jats:styled-content style="fixed-case">WGD</jats:styled-content> events.</jats:p></jats:list-item> <jats:list-item><jats:p>Diversification rates have been incredibly heterogeneous throughout the evolutionary history of angiosperms and reveal a pattern of ‘nested radiations’ – increases in net diversification nested within other radiations. This pattern in turn generates a negative relationship between clade age and diversity across both families and orders. We suggest that stochastically changing diversification rates across the phylogeny explain these patterns. Finally, we demonstrate significant statistical support for the <jats:styled-content style="fixed-case">WGD</jats:styled-content> radiation lag‐time model.</jats:p></jats:list-item> <jats:list-item><jats:p>Across angiosperms, nested shifts in diversification led to an overall increasing rate of net diversification and declining relative extinction rates through time. These diversification shifts are only rarely perfectly associated with <jats:styled-content style="fixed-case">WGD</jats:styled-content> events, but commonly follow them after a lag period.</jats:p></jats:list-item> </jats:list> </jats:p>

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