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. 2019 Jul 9;116(28):14083-14088.
doi: 10.1073/pnas.1903871116. Epub 2019 Jun 17.

A fully resolved backbone phylogeny reveals numerous dispersals and explosive diversifications throughout the history of Asteraceae

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A fully resolved backbone phylogeny reveals numerous dispersals and explosive diversifications throughout the history of Asteraceae

Jennifer R Mandel et al. Proc Natl Acad Sci U S A. .

Abstract

The sunflower family, Asteraceae, comprises 10% of all flowering plant species and displays an incredible diversity of form. Asteraceae are clearly monophyletic, yet resolving phylogenetic relationships within the family has proven difficult, hindering our ability to understand its origin and diversification. Recent molecular clock dating has suggested a Cretaceous origin, but the lack of deep sampling of many genes and representative taxa from across the family has impeded the resolution of migration routes and diversifications that led to its global distribution and tremendous diversity. Here we use genomic data from 256 terminals to estimate evolutionary relationships, timing of diversification(s), and biogeographic patterns. Our study places the origin of Asteraceae at ∼83 MYA in the late Cretaceous and reveals that the family underwent a series of explosive radiations during the Eocene which were accompanied by accelerations in diversification rates. The lineages that gave rise to nearly 95% of extant species originated and began diversifying during the middle Eocene, coincident with the ensuing marked cooling during this period. Phylogenetic and biogeographic analyses support a South American origin of the family with subsequent dispersals into North America and then to Asia and Africa, later followed by multiple worldwide dispersals in many directions. The rapid mid-Eocene diversification is aligned with the biogeographic range shift to Africa where many of the modern-day tribes appear to have originated. Our robust phylogeny provides a framework for future studies aimed at understanding the role of the macroevolutionary patterns and processes that generated the enormous species diversity of Asteraceae.

Keywords: Compositae; biogeography; molecular dating; phylogenomics.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Fig. 1.
Fig. 1.
Floral diversity of tribes. (A) Barnadesieae; (B) Famatinantheae; (C) Stifftieae; (D) Mutisieae; (E) Hecastocleideae; (F) Pertyeae; (G) Cardueae; (H) Vernonieae; and (I) Heliantheae. Photos of A, C, D, and H were provided by C.M.S.; B, image courtesy of J. Mauricio Bonifacino (photographer); E, by V.A.F.; F, image courtesy of Tiangang Gao (photographer); G, image courtesy of Alfonso Susanna (photographer); and I, by J.R.M.
Fig. 2.
Fig. 2.
Maximum likelihood tree for the Asteraceae family. Tree is color coded by subfamily with most tribes indicated in text to the right of each. Diamonds at nodes indicate bootstrap support of 94% or higher. All nodes along the backbone have maximal bootstrap support of 100%.
Fig. 3.
Fig. 3.
Tribe-level chronogram and ancestral range estimates. Probabilities for ancestral ranges are illustrated in pie charts color coded by geographic regions on the world map. Diversification rate shifts are indicated on the phylogeny with numbered boxes corresponding to the table above the geographic legend. Rate shift increases in red and downshifts are blue boxes. Species numbers per tribe are indicated to the Right of tribe names.

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