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Molecular Phylogenetics and Historical Biogeography of Basal Angiosperms PDF

227 Pages·2006·6.76 MB·English
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Molecular Phylogenetics and Historical Biogeography of Basal Angiosperms – A Case Study in Nymphaeales – Dissertation zur Erlangung des Doktorgrades (Dr. rer. nat.) der Mathematisch–Naturwissenschaftlichen Fakultät der Rheinischen Friedrich–Wilhelms–Universität Bonn vorgelegt von Cornelia Löhne aus Leipzig Bonn, März 2006 Angefertigt mit Genehmigung der Mathematisch–Naturwissenschaftlichen Fakultät der Rheinischen Friedrich-Wilhems-Universität Bonn. Erstgutachter: Prof. Dr. Wilhelm Barthlott Zweitgutachter: PD Dr. Thomas Borsch Tag der mündlichen Prüfung: 30.5.2006 Diese Dissertation ist auf dem Hochschulschriftenserver der ULB Bonn http://hss.ulb.uni-bonn.de/diss_online elektronisch publiziert. Erscheinungsjahr 2007 II Preface and Acknowledgements The present thesis was carried out in the framework of the Graduiertenkolleg “Evolution and Biodiversity in Time and Space” and supported by a graduate student fellowship from the Deutsche Forschungsgemeinschaft (DFG–Graduiertenkolleg 721), and supervised by Prof. Wilhelm Barthlott and Dr. habil. Thomas Borsch. The Graduiertenkolleg “Evolution and Biodiversity in Time and Space” united researchers and graduate students from the fields of organismic zoology, botany, developmental biology as well as palaeontology. In the course of several seminars and workshops all participants could exchange their specific knowledge and experience in fruitful discussions, broaden their horizons and get a wider picture on the diversity of organisms and their evolution. This innovative approach was extremely inspiring and provided a solid basis and backbone for my own interdisciplinary study. Many persons have been of great importance for this PhD project. First of all, I would like to express my gratitude to Prof. Wilhelm Barthlott. He gave me the chance to step into this integrative field of botany by inviting me to start this PhD project under his supervision in 2002. His stimulating fascination for the diversity of plants, together with his encouragement and support throughout the years were of great help. Also, I am indebted to Dr. Thomas Borsch, who introduced me into the world of phylogenetic systematics and molecular evolution. Without his continuous support and encouragement the present project would not have been possible. His valuable suggestions and comments on all parts of this thesis as well as his experience with the water lilies are greatly appreciated. Furthermore, I would like to express my gratitude to John Wiersema (US Department of Agriculture, Beltsville / USA), who was of great help for large parts of this thesis. My sincere thanks are for letting me benefit from his outstanding knowledge on the biology and diversity of water lilies. I am grateful to Prof. Klaus Peter Sauer and Prof. Thomas Litt (both University of Bonn), as well as to all other members of the Graduiertenkolleg for sharing their experience and for many stimulating discussions. Many thanks are due to Prof. Khidir W. Hilu (Virginia Tech, Blacksburg / USA) for valuable suggestions on the outline of this project. The molecular data sets in this thesis were produced in the Molecular Systematics Lab at the Nees Institute for Biodiversity of Plants in Bonn, which is led by Dr. Thomas Borsch. I wish to express my warmest thanks to all my colleagues: Dr. Kai Müller, Andreas Worberg, Dr. Dietmar Quandt, Dr. Rolf Blöcher, Kim Govers and Kassahun Tesfaye – thank you for all the assistance in the lab and at the PC, for interesting discussions and for much sympathy. The comments and suggestions of Kai Müller and Dietmar Quandt with regard to molecular IV evolution were especially helpful for the first part of my thesis. The respective chapter (2) profited also a lot from discussions with Prof. Volker Knoop (University of Bonn), Dr. Scot Kelchner (Idaho State University, Pocatello / USA) and Dr. Helga Ochoterena Booth (Universidad Nacional Autónoma de México). With regard to chapters 3 and 4, I am indebted to Dr. John Wiersema, Dr. Barre Hellquist (Massachusetts College of Liberal Arts, North Adams / USA) and Dr. Surrey Jacobs (Royal Botanical Gardens Sydney / Australia) for providing DNA material of several specimens of Nymphaea and Ondinea and for extremely useful comments on the results of the phylogenetic analyses. At this point I would also like to express my thanks to the Botanic Gardens of Bonn University, especially to Dr. Wolfram Lobin and to Michael Neumann, for curating and cultivating the living collection of water lilies, which was mainly established through collections of Dr. Thomas Borsch. The most integrative section of the present thesis is the last chapter, drawing a bow from phylogeny and extant distribution to the fossil record and biogeographic history. Therefore, I am indebted to many people who contributed to the completion of this part of the study. First, I would like to mention the BIOMAPS group of the Nees Institute, namely Dr. Jens Mutke, Holger Kreft, Dr. Wolfgang Küper and Henning Sommer. I could benefit a lot from their practical know-how in geographic information systems and from the long–standing experience and theoretical background in biodiversity mapping in this working group. I am also very grateful to PD Dr. Volker Wilde (Forschungsinstitut Senckenberg, Frankfurt / Germany), who shared his knowledge on earth history and the fossil record with me and provided valuable suggestions for the interpretation of the data. This last chapter of my thesis is an outcome of a close cooperation with Mi-Jeong Yoo (Soltis Lab, Florida Museum of Natural History / USA). Mi-Jeong Yoo has conducted most of the work on molecular dating of the Nymphaeales data set. I am very grateful to her for all the help, for the stimulating discussions and the introduction into cloning methods – but also for the good time I had during my stay at the Soltis Lab in Gainesville. I also sincerely thank Dr. Pamela Soltis and Prof. Douglas Soltis for their valuable suggestions, the encouraging support and their warm hospitality. Many thanks to Nils Köster, Holger Kreft, Nadja Korotkova and Andreas Worberg (all University of Bonn) for proof–reading. Last but not least I would like to express my deep gratitude to Dr. Tom Motzer for his untiring personal encouragement and loving support. Thanks for being there and for standing behind me. I very much enjoyed the time with you. Contents 1 General Introduction 1 1.1 Why work on basal angiosperms?............................................................................2 1.2 Hypotheses on the evolution and phylogeny of basal angiosperms.........................5 1.2.1 The origin and early diversification of angiosperms.....................................5 1.2.2 Pre–cladistic hypotheses on angiosperm diversification...............................8 1.2.3 Cladistic analyses and the changing view on angiosperm relationships.......9 1.2.4 Current understanding of phylogenetic relationships.................................10 1.3 The age of angiosperms.........................................................................................12 1.3.1 Evidence from the fossil record..................................................................12 1.3.2 Insights from molecular studies..................................................................14 1.4 Extant and historical biogeography of basal angiosperms.......................................15 1.5 Nymphaeales — the first globally diverse clade of angiosperms............................17 1.6 Aims of the study and project design.....................................................................20 2 Phylogeny of basal angiosperms based on the petD group II intron 23 2.1 Introduction...........................................................................................................24 2.2 Materials and Methods...........................................................................................26 2.2.1 Taxon sampling and plant material............................................................26 2.2.2 DNA isolation............................................................................................26 2.2.3 Primer design.............................................................................................26 2.2.4 Amplification and sequencing....................................................................29 2.2.5 Sequence alignment...................................................................................29 2.2.6 Coding of length mutational events............................................................31 2.2.7 Secondary structure....................................................................................33 2.2.8 Phylogenetic analysis.................................................................................33 2.3 Results...................................................................................................................35 2.3.1 Overall sequence variability.......................................................................35 2.3.2 Microstructural changes.............................................................................36 2.3.3 Secondary structure....................................................................................37 2.3.4 Trees obtained from individual and combined data partitions....................40 VI 2.4 Discussion.............................................................................................................42 2.4.1 Sequence variability within the petD region..............................................42 2.4.2 Kind and distribution of length mutations..................................................42 2.4.3 Structural effects on sequence evolution in the group II intron..................42 2.4.4 Molecular evolution of the spacer..............................................................46 2.4.5 Phylogenetic signal of petD sequence data................................................46 2.4.6 Phylogeny of basal angiosperms................................................................48 2.5 Conclusion............................................................................................................48 3 Phylogenetic analysis of Nymphaeales using fast–evolving and non–coding chloroplast markers 51 3.1 Introduction...........................................................................................................52 3.2 Materials and Methods..........................................................................................54 3.2.1 Taxon sampling and plant material............................................................54 3.2.2 DNA isolation, amplification and sequencing............................................57 3.2.3 Sequence alignment and indel coding.......................................................58 3.2.4 Phylogenetic analyses................................................................................58 3.3 Results...................................................................................................................60 3.3.1 Sequence variability observed in the data sets...........................................60 3.3.2 Trees obtained from different approaches..................................................62 3.3.3 Phylogeny of Nymphaeales.......................................................................66 3.3.4 Effects of taxon sampling...........................................................................66 3.4 Discussion.............................................................................................................68 3.4.1 Structure of data and reliability of the trees................................................68 3.4.2 Phylogeny and evolution of Nymphaeales.................................................70 3.4.3 Taxon sampling.........................................................................................73 3.4.4 Morphological characters in Nymphaeales................................................74 3.4.5 Phylogenetic signal of data partitions.........................................................74 4 Phylogenetic relationships among Australian water lilies (Nymphaea subg. Anecphya) 77 4.1 Introduction...........................................................................................................78 4.2 Materials and Methods..........................................................................................80 4.2.1 Taxon sampling and plant material............................................................80 4.2.2 DNA isolation, amplification and sequencing............................................80 4.2.3 Sequence alignment and phylogenetic analysis.........................................85 4.2.4 Biogeographic data....................................................................................85 4.3 Results...................................................................................................................86 4.3.1 Sequence variability in ITS.........................................................................86 4.3.2 Sequence variability of the trnT–trnF region..............................................89 VII 4.3.3 Trees obtained from nuclear ITS sequences...............................................90 4.3.4 Trees obtained from the plastid marker trnT–trnF.......................................94 4.4 Discussion.............................................................................................................98 4.4.1 Sequence variability and phylogenetic utility of trnT–trnF and ITS in Anecphya..................................................................................98 4.4.2 Polymorphic sites and incongruent trees provide evidence for reticulate evolution...............................................................................99 4.4.3 Phylogenetic relationships and reticulate evolution in Nymphaea subg. Anecphya.....................................................................102 4.4.4 The position of Ondinea purpurea...........................................................105 4.5 Conclusions and suggestions for further studies...................................................107 5 Biogeography of Nymphaeales: Extant patterns and historical events 109 5.1 Introduction.........................................................................................................110 5.1.1 Phylogeny and evolution of Nymphaeales...............................................111 5.1.2 The fossil record of Nymphaeales............................................................112 5.1.3 Geological settings...................................................................................114 5.1.4 Aims of this study.....................................................................................117 5.2 Materials and Methods.........................................................................................117 5.2.1 Taxon sampling and phylogenetic hypotheses.........................................117 5.2.2 Estimation of divergence times.................................................................118 5.2.3 Extant and fossil distribution....................................................................119 5.2.4 Dispersal–vicariance analysis...................................................................120 5.3 Results.................................................................................................................122 5.3.1 Extant distribution....................................................................................122 5.3.2 Estimated divergence times......................................................................126 5.3.3 Inferred ancestral areas.............................................................................127 5.4 Discussion...........................................................................................................132 5.4.1 Extant patterns of biodiversity in Nymphaeales........................................132 5.4.2 Divergence times in Nymphaeales and Nymphaeaceae...........................133 5.4.3 Ancestral areas and implications for possible dispersal scenarios.............135 5.4.4 Historical biogeography of Nymphaeales — a synthesis...........................136 5.5 Conclusion and prospect.....................................................................................144 Summary 147 References 149 List of Abbreviations 175 List of Figures 177 List of Tables 179 Appendix 181 VIII

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I also sincerely thank Dr. Pamela Soltis and. Prof. Douglas Soltis .. Angiosperms are still an “abominable mystery” (Darwin 1879) with respect to .. in North America the system of Charles Bessey (1845–1915) was most influential . Similarly.
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