Tangled webs and spider-flowers: Phylogenomics, biogeography, and seed morphology inform the evolutionary history of Cleomaceae.

Angiosperms353 Brassicales Cleomaceae continental disjunctions historical biogeography model clade phylogenomics seed morphology target capture

Journal

American journal of botany
ISSN: 1537-2197
Titre abrégé: Am J Bot
Pays: United States
ID NLM: 0370467

Informations de publication

Date de publication:
29 Aug 2024
Historique:
revised: 07 06 2024
received: 29 02 2024
accepted: 09 06 2024
medline: 31 8 2024
pubmed: 31 8 2024
entrez: 29 8 2024
Statut: aheadofprint

Résumé

Cleomaceae is an important model clade for studies of evolutionary processes including genome evolution, floral form diversification, and photosynthetic pathway evolution. Diversification and divergence patterns in Cleomaceae remain tangled as research has been restricted by its worldwide distribution, limited genetic sampling and species coverage, and a lack of definitive fossil calibration points. We used target sequence capture and the Angiosperms353 probe set to perform a phylogenetic study of Cleomaceae. We estimated divergence times and biogeographic analyses to explore the origin and diversification of the family. Seed morphology across extant taxa was documented with multifocal image-stacking techniques and morphological characters were extracted, analyzed, and compared to fossil records. We recovered a well-supported and resolved phylogenetic tree of Cleomaceae generic relationships that includes 236 (~86%) species. We identified 11 principal clades and confidently placed Cleomella as sister to the rest of the family. Our analyses suggested that Cleomaceae and Brassicaceae diverged ~56 mya, and Cleomaceae began to diversify ~53 mya in the Palearctic and Africa. Multiple transatlantic disjunct distributions were identified. Seeds were imaged from 218 (~80%) species in the family and compared to all known fossil species. Our results represent the most comprehensive phylogenetic study of Cleomaceae to date. We identified transatlantic disjunctions and proposed explanations for these patterns, most likely either long-distance dispersals or contractions in latitudinal distributions caused by climate change over geological timescales. We found that seed morphology varied considerably but mostly mirrored generic relationships.

Identifiants

pubmed: 39206557
doi: 10.1002/ajb2.16399
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e16399

Informations de copyright

© 2024 The Author(s). American Journal of Botany published by Wiley Periodicals LLC on behalf of Botanical Society of America.

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Auteurs

Theresa C Saunders (TC)

School of Biological Sciences, Washington State University, Pullman, Washington, 99164-4236, USA.

Isabel Larridon (I)

Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AE, UK.

William J Baker (WJ)

Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AE, UK.

Russell L Barrett (RL)

National Herbarium of New South Wales, Botanic Gardens of Sydney, Australian Botanic Garden, Locked Bag 6002, Mount Annan, 2567, New South Wales, Australia.
Evolution and Ecology Research Centre, School of Biological, Earth, and Environmental Sciences, University of New South Wales Sydney, Kensington, NSW 2052, Australia.

Félix Forest (F)

Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AE, UK.

Elaine Françoso (E)

Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AE, UK.
Centre for Ecology, Evolution and Behaviour, Department of Biological Sciences, School of Life Sciences and the Environment, Royal Holloway University of London, Egham, TW20 0EX, UK.

Olivier Maurin (O)

Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AE, UK.

Saba Rokni (S)

Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AE, UK.

Eric H Roalson (EH)

School of Biological Sciences, Washington State University, Pullman, Washington, 99164-4236, USA.

Classifications MeSH