The Ascomycota Tree of Life: A Phylum-wide Phylogeny Clarifies the Origin and Evolution of Fundamental Reproductive and Ecological Traits

Conrad L. Schoch(Oregon State University), Gi‐Ho Sung(Oregon State University), Francesc López‐Giráldez(Yale University), Jeffrey P. Townsend(Yale University), Jolanta Miądlikowska(Duke University), Valérie Hofstetter, Barbara Robbertse(Oregon State University), P. Brandon Matheny(Clark University), Frank Kauff(University of Kaiserslautern), Zheng Wang(Yale University), Cécile Gueidan(Westerdijk Fungal Biodiversity Institute), Rachael M. Andrie(Oregon State University), Kristin M. Trippe(Oregon State University), Linda M. Ciufetti(Oregon State University), Anja Amtoft Wynns(University of Copenhagen), Emily Fraker(Duke University), Brendan P. Hodkinson(Duke University), Gregory Bonito(Duke University), J.Z. Groenewald(Westerdijk Fungal Biodiversity Institute), Mahdi Arzanlou(University of Tabriz), Sybren de Hoog(Westerdijk Fungal Biodiversity Institute), P.W. Crous(Westerdijk Fungal Biodiversity Institute), David Hewitt(Harvard University), Donald H. Pfister(Harvard University), Kristin R. Peterson(Harvard University), Marieka Gryzenhout(University of Pretoria), Michael J. Wingfield(University of Pretoria), André Aptroot, Sung‐Oui Suh(American Type Culture Collection), Meredith Blackwell(Louisiana State University), David M. Hillis(The University of Texas at Austin), Gareth Griffith(Aberystwyth University), Lisa A. Castlebury(Agricultural Research Service), Amy Y. Rossman(Agricultural Research Service), H. Thorsten Lumbsch(Field Museum of Natural History), Robert Lücking(Field Museum of Natural History), Burkhard Büdel(University of Kaiserslautern), Alexandra Rauhut(University of Kaiserslautern), Paul Diederich(Musée National d'Histoire Naturelle), Damien Ertz(Meise Botanic Garden), David M. Geiser(Pennsylvania State University), Kentaro Hosaka(National Museum of Nature and Science), Patrik Inderbitzin(University of Nebraska at Kearney), Jan Kohlmeyer(University of North Carolina at Chapel Hill), Brigitte Volkmann‐Kohlmeyer(University of North Carolina at Chapel Hill), L. Mostert(Stellenbosch University), Kerry O’Donnell(Agricultural Research Service), Harrie J. M. Sipman(Botanic Garden and Botanical Museum Berlin), Jack D. Rogers(Washington State University), R. A. Shoemaker(Agriculture and Agri-Food Canada), Junta Sugiyama, Richard C. Summerbell(Victoria Park), Wendy A. Untereiner(Brandon University), Peter R. Johnston(Manaaki Whenua – Landcare Research), Soili Stenroos(University of Helsinki), Alga Zuccaro(Justus-Liebig-Universität Gießen), Paul S. Dyer(University of Nottingham), P. D. Crittenden(University of Nottingham), Mariette S. Cole, Karen Hansen(Swedish Museum of Natural History), James M. Trappe(Oregon State University), Rebecca Yahr(Royal Botanic Garden Edinburgh), François Lutzoni(Duke University), Joseph W. Spatafora(Oregon State University)
Systematic Biology
April 1, 2009
Cited by 662Open Access
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Abstract

We present a 6-gene, 420-species maximum-likelihood phylogeny of Ascomycota, the largest phylum of Fungi. This analysis is the most taxonomically complete to date with species sampled from all 15 currently circumscribed classes. A number of superclass-level nodes that have previously evaded resolution and were unnamed in classifications of the Fungi are resolved for the first time. Based on the 6-gene phylogeny we conducted a phylogenetic informativeness analysis of all 6 genes and a series of ancestral character state reconstructions that focused on morphology of sporocarps, ascus dehiscence, and evolution of nutritional modes and ecologies. A gene-by-gene assessment of phylogenetic informativeness yielded higher levels of informativeness for protein genes (RPB1, RPB2, and TEF1) as compared with the ribosomal genes, which have been the standard bearer in fungal systematics. Our reconstruction of sporocarp characters is consistent with 2 origins for multicellular sexual reproductive structures in Ascomycota, once in the common ancestor of Pezizomycotina and once in the common ancestor of Neolectomycetes. This first report of dual origins of ascomycete sporocarps highlights the complicated nature of assessing homology of morphological traits across Fungi. Furthermore, ancestral reconstruction supports an open sporocarp with an exposed hymenium (apothecium) as the primitive morphology for Pezizomycotina with multiple derivations of the partially (perithecia) or completely enclosed (cleistothecia) sporocarps. Ascus dehiscence is most informative at the class level within Pezizomycotina with most superclass nodes reconstructed equivocally. Character-state reconstructions support a terrestrial, saprobic ecology as ancestral. In contrast to previous studies, these analyses support multiple origins of lichenization events with the loss of lichenization as less frequent and limited to terminal, closely related species.


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