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The Evolutionary Ecology of Sprouting in Woody Plants
Open accessAbstract
Woody plants may be killed by severe disturbance or resprout from vegetative tissue. Sprouters can persist at a site through several generations of nonsprouters. Differences in sprouting behavior are therefore important for understanding vegetation dynamics, extinction risks, and woody plant management. Although sprouting appears not to be uniquely correlated with many other intrinsic attributes, such as specific leaf area or breeding systems, a clear correlate is reduced seedling aboveground growth rates from sprouters allocating more to belowground structures. Consequently, sprouters tend to have low seedling recruitment rates, and saplings take longer to reach maturity. Sprouters also tend to have lower seed output than nonsprouters, but comparative studies have seldom taken other trait differences such as plant size into account. Added to these trade‐offs between persistence and recruitment, sprouters are often multistemmed and shorter than related nonsprouters and may be outcompeted by them when disturbances are rare. Since sprouters tend to have long generation times, damped demographic trends, and gene flow across generations, it has been suggested that their speciation rates would be low. The available data, primarily from fire‐prone Gondwanan shrublands in South Africa, show no strong differences in speciation rates of related sprouters versus seeders. This indicates that ecological factors are important determinants of the evolution of fire life histories. Analysis of disturbance regimes indicates a fundamental ecological correlate: sprouters are favored where disturbance regimes are frequent and severe in comparison to regrowth rates. To bridge the gap between ecology and evolution, data are needed on the genetical differences between related species with contrasting sprouter life histories.
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Citations
Cites
A leaf-height-seed (LHS) plant ecology strategy scheme
Westoby, M. (1998) · Plant and Soil · doi:10.1023/a:1004327224729 · Cited by 1,925 · cited 1×
“Sprouting has not been included in general functional type systems such as those of Grime (1979; Grime et al. 1997) or Westoby (1998).”
Background
Cited by
Fire as a global ‘herbivore’: the ecology and evolution of flammable ecosystems
BOND, W., & KEELEY, J. (2005) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2005.04.025 · Cited by 2,484
Self-citationCommunity Assembly, Niche Conservatism, and Adaptive Evolution in Changing Environments
Ackerly, D. D. (2003) · International Journal of Plant Sciences · doi:10.1086/368401 · Cited by 893
Fire and the spread of flowering plants in the Cretaceous
Bond, W. J., & Scott, A. C. (2010) · New Phytologist · doi:10.1111/j.1469-8137.2010.03418.x · Cited by 239
Self-citationUpdating models for restoration and management of fiery ecosystems
Fill, J. M., Platt, W. J., Welch, S. M., Waldron, J. L., & Mousseau, T. A. (2015) · Forest Ecology and Management · doi:10.1016/j.foreco.2015.07.021 · Cited by 63
Morales, D., Rostagno, C. M., & La Manna, L. (2013) · Plant and Soil · doi:10.1007/s11104-013-1640-1 · Cited by 24
Metadata
- Authors
- Bond, W. J., & Midgley, J. J.
- Venue
- International Journal of Plant Sciences
- Publisher
- University of Chicago Press
- Published
- 2003-05
- Volume
- 164
- Issue
- S3
- Pages
- S103-S114
- ISSN
- 1058-5893 (ISSN-L)
- 1537-5315
- OpenAlex
- W1988048216
- Cited by
- 392
- References
- 1
- FWCI
- 11.42
- Type
- journal article
- Language
- en
- Open access
- green
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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