Comprehensive phylogenomic time tree of bryophytes reveals deep relationships and uncovers gene incongruences in the last 500 million years of diversification

Author:

Bechteler Julia12ORCID,Peñaloza‐Bojacá Gabriel3ORCID,Bell David4ORCID,Gordon Burleigh J.5ORCID,McDaniel Stuart F.5ORCID,Christine Davis E.5,Sessa Emily B.5ORCID,Bippus Alexander6ORCID,Christine Cargill D.7ORCID,Chantanoarrapint Sahut8ORCID,Draper Isabel9ORCID,Endara Lorena5ORCID,Forrest Laura L.4ORCID,Garilleti Ricardo10ORCID,Graham Sean W.11ORCID,Huttunen Sanna12ORCID,Lazo Javier Jauregui13ORCID,Lara Francisco9ORCID,Larraín Juan14ORCID,Lewis Lily R.5ORCID,Long David G.4ORCID,Quandt Dietmar1ORCID,Renzaglia Karen15ORCID,Schäfer‐Verwimp Alfons16ORCID,Lee Gaik Ee17ORCID,Sierra Adriel M.18ORCID,von Konrat Matt19ORCID,Zartman Charles E.20ORCID,Pereira Marta Regina21ORCID,Goffinet Bernard22ORCID,Villarreal A. Juan Carlos18ORCID

Affiliation:

1. Nees‐Institute for Plant Biodiversity University of Bonn Meckenheimer Allee 170 53115 Bonn Germany

2. Plant Biodiversity and Ecology, iES Landau, Institute for Environmental Sciences RPTU University of Kaiserslautern‐Landau Fortstraße 7 76829 Landau Germany

3. Laboratório de Sistemática Vegetal, Departamento de Botânica, Instituto de Ciências Biológicas Universidade Federal de Minas Gerais Brazil

4. Royal Botanic Garden Edinburgh 20A Inverleith Row Edinburgh EH3 5LR UK

5. Department of Biological Sciences University of Florida 220 Bartram Hall Gainesville FL 32611 USA

6. California State Polytechnic University Humboldt Arcata CA 95521 USA

7. Australian National Herbarium Centre for Australian National Biodiversity Research GPO Box 1700 Canberra ACT 2601 Australia

8. PSU Herbarium, Division of Biological Science Faculty of Science Prince of Songkla University Hat Yai Songkhla 90110 Thailand

9. Departamento de Biología, Facultad de Ciencias Universidad Autónoma de Madrid, 28049 Madrid, Spain/Centro de Investigación en Biodiversidad y Cambio Global, Universidad Autónoma de Madrid 28049 Madrid Spain

10. Departamento de Botánica y Geología. Universidad de Valencia Avda. Vicente Andrés Estelles s/n 46100 Burjassot Spain

11. Department of Botany University of British Columbia 6270 University Boulevard Vancouver British Columbia V6T 1Z4 Canada

12. Herbarium (TUR), Biodiversity Unit 20014 University of Turku Finland

13. Department of Plant Biology and Genome Center University of California Davis 451 Health Sciences Drive Davis CA 95616 USA

14. Centro de Investigación en Recursos Naturales y Sustentabilidad (CIRENYS) Universidad Bernardo O'Higgins Avenida Viel 1497 Santiago Chile

15. Department of Plant Biology Southern Illinois University Carbondale IL 62901 USA

16. Mittlere Letten 11, 88634 Herdwangen‐Schönach Germany

17. Faculty of Science and Marine Environment/Institute of Tropical Biodiversity and Sustainable Development Universiti Malaysia Terengganu 21020 Kuala Nerus Terengganu Malaysia

18. Département de Biologie Université Laval Québec Québec G1V 0A6 Canada

19. Gantz Family Collections Center Field Museum 1400 S. DuSable Lake Shore Drive Chicago IL 60605 USA

20. Instituto Nacional de Pesquisas da Amazônia, Departamento de Biodiversidade Avenida André Araújo, 2936, Aleixo, CEP 69060‐001 Manaus AM Brazil

21. Universidade do Estado do Amazonas Av. Djalma Batista, 2470, Chapada Manaus 69050‐010 Amazonas Brazil

22. Ecology and Evolutionary Biology University of Connecticut 75 North Eagleville Road Storrs CT 06269‐3043 USA

Abstract

AbstractPremiseBryophytes form a major component of terrestrial plant biomass, structuring ecological communities in all biomes. Our understanding of the evolutionary history of hornworts, liverworts, and mosses has been significantly reshaped by inferences from molecular data, which have highlighted extensive homoplasy in various traits and repeated bursts of diversification. However, the timing of key events in the phylogeny, patterns, and processes of diversification across bryophytes remain unclear.MethodsUsing the GoFlag probe set, we sequenced 405 exons representing 228 nuclear genes for 531 species from 52 of the 54 orders of bryophytes. We inferred the species phylogeny from gene tree analyses using concatenated and coalescence approaches, assessed gene conflict, and estimated the timing of divergences based on 29 fossil calibrations.ResultsThe phylogeny resolves many relationships across the bryophytes, enabling us to resurrect five liverwort orders and recognize three more and propose 10 new orders of mosses. Most orders originated in the Jurassic and diversified in the Cretaceous or later. The phylogenomic data also highlight topological conflict in parts of the tree, suggesting complex processes of diversification that cannot be adequately captured in a single gene‐tree topology.ConclusionsWe sampled hundreds of loci across a broad phylogenetic spectrum spanning at least 450 Ma of evolution; these data resolved many of the critical nodes of the diversification of bryophytes. The data also highlight the need to explore the mechanisms underlying the phylogenetic ambiguity at specific nodes. The phylogenomic data provide an expandable framework toward reconstructing a comprehensive phylogeny of this important group of plants.

Publisher

Wiley

Subject

Plant Science,Genetics,Ecology, Evolution, Behavior and Systematics

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