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dc.contributor.authorAgrawal, Anurag A.
dc.contributor.authorFishbein, Mark
dc.contributor.authorHalitschke, Rayko
dc.contributor.authorHastings, Amy P.
dc.contributor.authorRabosky, Daniel L.
dc.contributor.authorRasmann, Sergio
dc.date.accessioned2019-08-02T13:06:45Z
dc.date.available2019-08-02T13:06:45Z
dc.date.issued2009-10-27
dc.identifier.urihttps://hdl.handle.net/1813/66747
dc.description.abstractOne signature of adaptive radiation is a high level of trait change early during the diversification process and a plateau toward the end of the radiation. Although the study of the tempo of evolution has historically been the domain of paleontologists, recently developed phylogenetic tools allow for the rigorous examination of trait evolution in a tremendous diversity of organisms. Enemy-driven adaptive radiation was a key prediction of Ehrlich and Raven's coevolutionary hypothesis [Ehrlich PR, Raven PH (1964) Evolution 18:586–608], yet has remained largely untested. Here we examine patterns of trait evolution in 51 North American milkweed species (Asclepias), using maximum likelihood methods. We study 7 traits of the milkweeds, ranging from seed size and foliar physiological traits to defense traits (cardenolides, latex, and trichomes) previously shown to impact herbivores, including the monarch butterfly. We compare the fit of simple random-walk models of trait evolution to models that incorporate stabilizing selection (Ornstein-Ulenbeck process), as well as time-varying rates of trait evolution. Early bursts of trait evolution were implicated for 2 traits, while stabilizing selection was implicated for several others. We further modeled the relationship between trait change and species diversification while allowing rates of trait evolution to vary during the radiation. Species-rich lineages underwent a proportionately greater decline in latex and cardenolides relative to species-poor lineages, and the rate of trait change was most rapid early in the radiation. An interpretation of this result is that reduced investment in defensive traits accelerated diversification, and disproportionately so, early in the adaptive radiation of milkweeds
dc.description.sponsorshipOur research and laboratories are supported by National Science Foundation-Division of Environmental Biology Grants 0447550 and 0608686.
dc.language.isoen_US
dc.publisherNational Academy of Sciences
dc.relation.ispartofseriesProceedings of the National Academy of Sciences
dc.relation.hasversionAgrawal, A. A., Fishbein, M., Halitschke, R., Hastings, A. P., Rabosky, D. L., & Rasmann, S. (2009). Evidence for adaptive radiation from a phylogenetic study of plant defenses. Proceedings of the National Academy of Sciences, 106(43), 18067–18072.
dc.subjectAsclepias
dc.subjectcardenolides
dc.subjectcoevolution
dc.subjectmacroevolutionary trends
dc.subjectlatex
dc.titleEvidence for adaptive radiation from a phylogenetic study of plant defenses
dc.typearticle
dcterms.licensehttps://hdl.handle.net/1813/60291
dc.relation.doihttps://doi.org/10.1073/pnas.0904862106


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