The DOI matches its Crossref record; 119 of the 119 references it cites were found in a registry or an index.
Community Assembly, Niche Conservatism, and Adaptive Evolution in Changing Environments
Abstract
The widespread correspondence between phenotypic variation and environmental conditions, the "fit" of organisms to their environment, reflects the adaptive value of plant functional traits. Several processes contribute to these patterns: plasticity, ecological sorting, and adaptive evolution. This article addresses the importance of ecological sorting processes (community assembly, migration, habitat tracking, etc.) as primary causes of functional trait distributions at the local and landscape level. In relatively saturated communities, plants will establish and regenerate in environments to which they are well adapted, so their distributions, and the distributions of associated functional traits, will reflect the distribution of optimal or near‐optimal environmental conditions in space and time. The predicted evolutionary corollary of this process is that traits related to habitat occupancy, e.g., environmental tolerances, will be under stabilizing selection. This process contributes to the widely observed pattern of phylogenetic niche conservatism, i.e., ecological and phenotypic similarities of closely related species. Evidence for niche conservatism in plants is reviewed. Based on Jackson and Overpeck's concept of the realized environment, I propose three scenarios in which a species' distributional responses to environmental conditions will lead to a "mismatch" between its environmental tolerances and the environments it occupies, thus creating opportunities for adaptive evolution: (1) the colonization of "environmental islands" (habitats that are discontinuous in niche space) that require large adaptive shifts in tolerance of one or more environmental factors; (2) the persistence of "trailing‐edge" populations in species tracking changing climate, if barriers to dispersal of competitors prevent competitive exclusion in the deteriorating conditions; and (3) responses to changes in the realized environment in multidimensional niche space, in which species are predicted to track environmental factors for which they exhibit narrow tolerances and exhibit adaptive evolutionary response along axes where they exhibit greater niche breadth. These three scenarios provide a conceptual framework that emphasizes the role of ecological sorting processes and stabilizing selection as the context for understanding opportunities for adaptive evolution in heterogeneous and changing environments.
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Citations
Cites
The genetic legacy of the Quaternary ice ages
Hewitt, G. (2000) · Nature · doi:10.1038/35016000 · Cited by 7,127
The Unified Neutral Theory of Biodiversity and Biogeography
Jetschke, G. (2002) · Ecology · doi:10.1890/0012-9658(2002)083[1771:tuntob]2.0.co;2 · Cited by 6,993
Hutchinson, G. E. (1957) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1957.022.01.039 · Cited by 6,228
Grime, J. P. (1977) · The American Naturalist · doi:10.1086/283244 · Cited by 5,754 · cited 1×
“…of contrasting ecological characteristics of pioneer versus persistent, late-successional species, may also play a large role in maintaining plant diversity (Tilman 1994) and thus help maintain high levels of trait diversity within communities (Grime 1977; Bazzaz 1979; Rees and Westboy 1997).”
BackgroundExaptation—a missing term in the science of form
Gould, S. J., & Vrba, E. S. (1982) · Paleobiology · doi:10.1017/s0094837300004310 · Cited by 5,136
The comparative method in evolutionary biology
(1992) · Choice Reviews Online · doi:10.5860/choice.29-5104 · Cited by 4,931
TESTING FOR PHYLOGENETIC SIGNAL IN COMPARATIVE DATA: BEHAVIORAL TRAITS ARE MORE LABILE
Blomberg, S. P., Garland, T., & Ives, A. R. (2003) · Evolution · doi:10.1111/j.0014-3820.2003.tb00285.x · Cited by 4,678
Phylogenies and Community Ecology
Webb, C. O., Ackerly, D. D., McPeek, M. A., & Donoghue, M. J. (2002) · Annual Review of Ecology and Systematics · doi:10.1146/annurev.ecolsys.33.010802.150448 · Cited by 4,609
Self-citationEvolutionary Significance of Phenotypic Plasticity in Plants
Bradshaw, A. D. (1965) · Advances in Genetics · doi:10.1016/s0065-2660(08)60048-6 · Cited by 3,124
Plant Ecological Strategies: Some Leading Dimensions of Variation Between Species
Westoby, M., Falster, D. S., Moles, A. T., Vesk, P. A., & Wright, I. J. (2002) · Annual Review of Ecology and Systematics · doi:10.1146/annurev.ecolsys.33.010802.150452 · Cited by 3,069
Cited by
The merging of community ecology and phylogenetic biology
Cavender‐Bares, J., Kozak, K. H., Fine, P. V. A., & Kembel, S. W. (2009) · Ecology Letters · doi:10.1111/j.1461-0248.2009.01314.x · Cited by 2,321
SUDING, K. N., LAVOREL, S., CHAPIN, F. S., CORNELISSEN, J. H. C., DÍAZ, S., GARNIER, E., GOLDBERG, D., HOOPER, D. U., JACKSON, S. T., & NAVAS, M. (2008) · Global Change Biology · doi:10.1111/j.1365-2486.2008.01557.x · Cited by 1,285
Garnier, E., & Navas, M.-L. (2012) · Agronomy for Sustainable Development · doi:10.1007/s13593-011-0036-y · Cited by 490
Mainali, K. P., Warren, D. L., Dhileepan, K., McConnachie, A., Strathie, L., Hassan, G., Karki, D., Shrestha, B. B., & Parmesan, C. (2015) · Global Change Biology · doi:10.1111/gcb.13038 · Cited by 314
The geography and ecology of plant speciation: range overlap and niche divergence in sister species
Anacker, B. L., & Strauss, S. Y. (2014) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2013.2980 · Cited by 307
Metadata
- Authors
- Ackerly, D. D.
- Venue
- International Journal of Plant Sciences
- Publisher
- University of Chicago Press
- Published
- 2003-05
- Volume
- 164
- Issue
- S3
- Pages
- S165-S184
- ISSN
- 1058-5893 (ISSN-L)
- 1537-5315
- OpenAlex
- W2015340512
- Cited by
- 893
- References
- 119
- FWCI
- 12.91
- Type
- journal article
- Language
- en
- Open access
- closed
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