Published October 22, 2014 | Version v1
Dataset Open

Data from: Three keys to the radiation of angiosperms into freezing environments

  • 1. University of Washington
  • 2. University of Idaho
  • 3. Department of Ecological Sciences, Systems Ecology, de Boelelaan 1085, 1081 HV Amsterdam, the Netherlands,*
  • 4. University of Michigan-Ann Arbor
  • 5. University of British Columbia
  • 6. Utah State University
  • 7. University of Tennessee at Knoxville
  • 8. Environmental Earth Sciences
  • 9. University of Minnesota
  • 10. Wesleyan University
  • 11. University of Florida
  • 12. University of Missouri–St. Louis
  • 13. Macquarie University
  • 14. Queen's University
  • 15. College of the Holy Cross
  • 16. Royal Botanic Gardens
  • 17. Florida Museum of Natural History
  • 18. Department of Plant Biology
  • 19. National Institute for Mathematical and Biological Synthesis

Description

Early flowering plants are thought to have been woody species restricted to warm habitats1, 2, 3. This lineage has since radiated into almost every climate, with manifold growth forms4. As angiosperms spread and climate changed, they evolved mechanisms to cope with episodic freezing. To explore the evolution of traits underpinning the ability to persist in freezing conditions, we assembled a large species-level database of growth habit (woody or herbaceous; 49,064 species), as well as leaf phenology (evergreen or deciduous), diameter of hydraulic conduits (that is, xylem vessels and tracheids) and climate occupancies (exposure to freezing). To model the evolution of species' traits and climate occupancies, we combined these data with an unparalleled dated molecular phylogeny (32,223 species) for land plants. Here we show that woody clades successfully moved into freezing-prone environments by either possessing transport networks of small safe conduits5 and/or shutting down hydraulic function by dropping leaves during freezing. Herbaceous species largely avoided freezing periods by senescing cheaply constructed aboveground tissue. Growth habit has long been considered labile6, but we find that growth habit was less labile than climate occupancy. Additionally, freezing environments were largely filled by lineages that had already become herbs or, when remaining woody, already had small conduits (that is, the trait evolved before the climate occupancy). By contrast, most deciduous woody lineages had an evolutionary shift to seasonally shedding their leaves only after exposure to freezing (that is, the climate occupancy evolved before the trait). For angiosperms to inhabit novel cold environments they had to gain new structural and functional trait solutions; our results suggest that many of these solutions were probably acquired before their foray into the cold.

Notes

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Additional details

Related works

Is cited by
10.1038/nature12872 (DOI)