Phylogenetic Classification of Seed Plants of Taiwan

Total Page:16

File Type:pdf, Size:1020Kb

Phylogenetic Classification of Seed Plants of Taiwan Lin and Chung Bot Stud (2017) 58:52 DOI 10.1186/s40529-017-0206-6 ORIGINAL ARTICLE Open Access Phylogenetic Classifcation of Seed Plants of Taiwan Cheng‑Tao Lin1 and Kuo‑Fang Chung2* Abstract Background: Biological classifcation, the hierarchical arrangement of scientifc names of organisms, constitutes the core infrastructure of biological databases. For an efcient management of biological databases, adopting a stable and universal biological classifcation system is crucial. Currently in Taiwan Biodiversity Information Facility (TaiBIF; http://taibif.tw/), the national portal website that integrates Taiwan’s biodiversity information databases, angiosperms are arranged according to Cronquist’s System of Classifcation, which is not compatible with current trend of the Angiosperm Phylogeny Group (APG) classifcation. To consolidate the function and management of the database, TaiBIF is moving to adopt the APG IV classifcation and Christenhusz et al. (Phytotaxa 19:55–70, 2011)’s classifcation of gymnosperms, which we summarize as the Phylogenetic Classifcation of Seed Plants of Taiwan. Results: The Phylogenetic Classifcation of Seed Plants of Taiwan places gymnosperms in fve families [vs. eight families in the Flora of Taiwan (FOT)] and angiosperms in 210 families (vs. 193 families in FOT). Three FOT gymnosperm families are synonymized in current treatment. Of the 210 APG IV families, familial circumscriptions of 114 families are identical with FOT and 50 families are recircumscription of FOT, with 46 families newly added. Of the 29 FOT families not included in current classifcation, two families are excluded and 27 families are synonymized. Conclusions: The adoption of the Phylogenetic Classifcation of Seed Plants of Taiwan in TaiBIF will provide better service and efcient management of the nation’s biodiversity information databases. Keywords: Angiosperm Phylogeny Group classifcation, APG IV, Big new biology, Data cleaning, Flowering plants, Gymnosperms, Spermatophytina, TaiBIF, TaiCOL Background 2013) through TaiCOL (Catalogue of Life in Taiwan; Biological classifcation, the hierarchical arrangement of http://col.taibif.tw/), TaiEOL (Taiwan Encyclopedia of scientifc names of organisms, provides keywords and Life; http://eol.taibif.tw/), TaiBOL (Cryobanking Pro- links to catalogue and organize biological information gram for Wildlife Genetic Material in Taiwan; http:// (Patterson et al. 2014). Biological classifcation consti- cryobank.museum.biodiv.tw/), and TELDAP (Taiwan tutes the core infrastructure of biological databases (Pat- e-Learning and Digital Archives Programs; http://core. terson et al. 2010, 2014). Adopting a stable and universal teldap.tw/). As an associate participant of GBIF (Global biological classifcation system not only is crucial for the Biodiversity Information Facility; http://www.gbif.org/), users but also fundamental for the efcient management TaiBIF also functions as a national node of GBIF (Shao of the databases. et al. 2013). Te initiation of TaiBIF started in 2003 with TaiBIF (Taiwan Biodiversity Information Facility; the establishment of TaiBNET (Taiwan Biodiversity http://taibif.tw/) is the national portal website that inte- National Information Network; http://taibnet.sinica. grates Taiwan’s biodiversity information (Shao et al. edu.tw), providing “Taiwan species checklist” and the list of local taxonomic experts (Shao et al. 2013). Cur- *Correspondence: [email protected] rently in TaiCOL, the successor of TaiBNET, the fower- 2 Research Museum and Herbarium (HAST), Biodiversity Research Center, ing plants are arranged according to Cronquist (1968)’s Academia Sinica, Taipei 11529, Taiwan System of Classifcation (Shao et al. 2008), replacing A. Full list of author information is available at the end of the article © The Author(s) 2017. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. Lin and Chung Bot Stud (2017) 58:52 Page 2 of 14 Engler’s Syllabus der Pfanzenfamilien that was adopted as a basis for migrating process. Te migration process in the Flora of Taiwan (FOT), 2nd edition (Huang 1994). applied a ‘data cleaning framework’ to improve our data Although Cronquist’s System was highly infuential and set quality through diagnosing, detecting, and correcting had been followed by several major foras such as Flora procedures. Te data cleaning procedure included three of North America (Reveal 1993) and Flora of Australia major stages: (1) error type defning, (2) error instance (Kanis et al. 1999), much of the content of Cronquist Sys- identifying, and (3) error correcting (Maletic and Mar- tem is not compatible to the current trend of the APG cus 2000). Furthermore, we followed the data cleaning classifcation. principles and methods suggested by Chapman (2005) Te Angiosperm Phylogeny Group (APG) classifcation when processing nomenclature data. In the initial stage of the orders and families of fowering plants, now in its of migration, instead of constructing a name-based data- fourth edition (APG IV), is a collaborative efort of plant base, a taxon-based database, which includes a unique molecular systematic community worldwide (Te Angi- taxonomy identifer (taxon ID) and several attributes osperm Phylogeny Group 1998, 2003, 2009, 2016), pro- such as family, genus, scientifc names and vernacu- viding the greatest stability and predictability regarding lar names, etc., was constructed. In order to reduce the biodiversity information of fowering plants (Mayr 1981; redundancy of the database and improve the data qual- Wearn et al. 2013). Although APG classifcation has not ity and integrity, we adopted relational database normali- been adopted ofcially in Taiwan, families circumscribed zation to parse the raw data table into a second normal by molecular phylogenetic studies and summarized by form schema. Trough the normalization process, poten- APG have been increasingly accepted by both academic tial errors such as duplicate entries, misplaced taxa, etc., (Hsu et al. 2011, 2016a, b; Wu et al. 2015) and citizen could be eliminated efciently. In the second stage, we scientists (e.g., Nature Campus http://nc.biodiv.tw/bbs/ automated a python script to cross-validate our data index.php). base with Missouri Botanical Garden’s Tropicos (http:// As an ofcial provider of biodiversity information of www.tropicos.org/) and International Plant Names the country, the classifcation systems followed by Tai- Index (IPNI, http://ipni.org), identifying unmatched or COL has deep and profound infuences. In an efort to unfound names for manual checking. In the third stage, consolidate the function and management of TaiBIF that three major possible errors or problems: (1) illegitimate shall result in stable and better services of the websites, or invalid names, (2) misspelled names, (3) diferent taxo- it is inevitable for TaiCOL to adopt classifcation systems nomic treatment, were corrected after cross-validation. that are constructed based on results of robust molecular We adopted Ruggiero et al. (2015) for the higher level phylogenetic analyses. Tis article outlines phylogenetic classifcation of seed plants (Subphylum Spermatophy- classifcation of families of the seed plants of Taiwan tina and above). For gymnosperms (Superclass Gymno- summarized based on Christenhusz et al. (2011)’s clas- spermae), Christenhusz et al. (2011)’s classifcation was sifcation of gymnosperms, APG IV, and subsequent followed, though caution was taken for the uncertainty studies. To facilitate the transition toward APG IV, we of the phylogenetic position of gnetophytes (Lu et al. also provide the spreadsheet of the classifcation schema 2014; Wang and Ran 2014). For angiosperms (Superclass for all seed plant genera that will be adopted by TaiCOL Angiospermae), major clades recognized as superorders (Additional fle 1: Appendix S1). Tis spreadsheet will be in Chase and Reveal (2009) and the classifcation of Te updated constantly and can be downloaded through Tai- Angiosperm Phylogeny Group (2016) was adopted, with COL. A brief note is provided for families of which cir- the exception of Boraginales in which Luebert et al. cumscription has been changed between the treatment of (2016)’s new familial classifcation was followed. For FOT and APG IV classifcation. orders and families of which vernacular names are lack- ing in the current literature of the fora of Taiwan, the Methods names proposed by Liu et al. (2015) were followed. Te database of seed plants of Taiwan was compiled from “a checklist of the vascular plants of Taiwan” of the Results and discussion Flora of Taiwan (Bouford et al. 2003), “Illustrated Guide Based on Christenhusz et al. (2011), APG IV (2016), and to Aquatic Plants of Taiwan” (Yang et al. 2001), Wu et al. Luebert et al. (2016)’s familial classifcation of Boragina- (2010) that summarized naturalized and invasive fora, les, the “Phylogenetic Classifcation of Seed Plants of Tai- subsequently published native (e.g., Hsu et al. 2011; Wu wan” is presented below. Of the four classes (I–IV), eight et al. 2015) and naturalized (e.g., Liang et al. 2011; Wang orders (A–H), and 12 families of gymnosperms in Chris- et al. 2016) species, and the fora of Tongsha (Pratas) tenhusz et al. (2011)’s
Recommended publications
  • Growing Plants for Hawaiian Lei ‘A‘Ali‘I
    6 Growing Plants for Hawaiian Lei ‘a‘ali‘i OTHER COMMON NAMES: ‘a‘ali‘i kū range of habitats from dunes at sea makani, ‘a‘ali‘i kū ma kua, kū- level up through leeward and dry makani, hop bush, hopseed bush forests and to the highest peaks SCIENTIFIC NAME: Dodonaea viscosa CURRENT STATUS IN THE WILD IN HAWAI‘I: common FAMILY: Sapindaceae (soapberry family) CULTIVARS: female cultivars such as ‘Purpurea’ and ‘Saratoga’ have NATURAL SETTING/LOCATION: indigenous, been selected for good fruit color pantropical species, found on all the main Hawaiian Islands except Kaho‘olawe; grows in a wide Growing your own PROPAGATION FORM: seeds; semi-hardwood cuttings or air layering for selected color forms PREPLANTING TREATMENT: step on seed capsule to release small, round, black seeds, or use heavy gloves and rub capsules vigorously between hands; put seeds in water that has been brought to a boil and removed from heat, soak for about 24 hours; if seeds start to swell, sow imme- diately; discard floating, nonviable seeds; use strong rooting hormone on cuttings TEMPERATURE: PLANTING DEPTH: sow seeds ¼" deep in tolerates dry heat; tem- after fruiting period to shape or keep medium; insert base of cutting 1–2" perature 32–90°F short; can be shaped into a small tree or maintained as a shrub, hedge, or into medium ELEVATION: 10–7700' espalier (on a trellis) GERMINATION TIME: 2–4 weeks SALT TOLERANCE: good (moderate at SPECIAL CULTURAL HINTS: male and female CUTTING ROOTING TIME: 1½–3 months higher elevations) plants are separate, although bisex- WIND RESISTANCE:
    [Show full text]
  • A New Species of Saurauia (Actinidiaceae) from Jharkhand State, India
    J. Jpn. Bot. 84: 233–236 (2009) A New Species of Saurauia (Actinidiaceae) from Jharkhand State, India Vinay ranjan and S. C. srivastava Central National Herbarium, Botanical Survey of India Howrah–711103, INDIA E-mail: [email protected] (Received on November 25, 2008) Saurauia parasnathensis V. Ranjan & S. C. Srivastava is described from India as new to science. This species is characterized by having cymose inflorescence with many- flowered fascicles, yellow flowers and 27–35 stamens in two rows. Key words: Actinidiaceae, India, new species, Saurauia. Saurauia Willd., comprising of 300 27–35 stamens in two rows. species (Mabberley 2005), is distributed in tropical Asia and America (Cuong et al. 2007, Saurauia parasnathensis V. Ranjan & Dressler and Bayer 2004, Soejarto 2004). S. C. Srivastava, sp. nov. [Figs. 1, 2] Hooker (1874) and Paul (1993) described Specibus differt aliis Saurauia cerea eight species from British India and India, Dyer petalis flavis, inflorescentiae cymosae respectively. While collecting the materials for multifloris fasciculis et staminibus 27–35 flora of Parasnath Wildlife Sanctuary, Giridih bistratus ornata. District, Jharkhand State, India between Type: INDIA: Jharkhand State, Giridih 2004 and 2006, the first author collected District, Parasnath Wildlife Sanctuary, alt. an interesting tree species of ca.10 m high, ca.1200 m, 21 March 2005, Vinay Ranjan leafless in flowering during the month of 37947A (holotype–CAL), 37947B (isotype– March, on the hill top. A search of Indian CAL). herbaria and literature revealed that it belongs Trees up to 10 m high, branchlets to the genus Saurauia Willd. (Actinidiaceae), brownish-black with ruptured bark and scars but the characters do not match with any of inflorescence.
    [Show full text]
  • Pu'u Wa'awa'a Biological Assessment
    PU‘U WA‘AWA‘A BIOLOGICAL ASSESSMENT PU‘U WA‘AWA‘A, NORTH KONA, HAWAII Prepared by: Jon G. Giffin Forestry & Wildlife Manager August 2003 STATE OF HAWAII DEPARTMENT OF LAND AND NATURAL RESOURCES DIVISION OF FORESTRY AND WILDLIFE TABLE OF CONTENTS TITLE PAGE ................................................................................................................................. i TABLE OF CONTENTS ............................................................................................................. ii GENERAL SETTING...................................................................................................................1 Introduction..........................................................................................................................1 Land Use Practices...............................................................................................................1 Geology..................................................................................................................................3 Lava Flows............................................................................................................................5 Lava Tubes ...........................................................................................................................5 Cinder Cones ........................................................................................................................7 Soils .......................................................................................................................................9
    [Show full text]
  • Outline of Angiosperm Phylogeny
    Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese
    [Show full text]
  • Alphabetical Lists of the Vascular Plant Families with Their Phylogenetic
    Colligo 2 (1) : 3-10 BOTANIQUE Alphabetical lists of the vascular plant families with their phylogenetic classification numbers Listes alphabétiques des familles de plantes vasculaires avec leurs numéros de classement phylogénétique FRÉDÉRIC DANET* *Mairie de Lyon, Espaces verts, Jardin botanique, Herbier, 69205 Lyon cedex 01, France - [email protected] Citation : Danet F., 2019. Alphabetical lists of the vascular plant families with their phylogenetic classification numbers. Colligo, 2(1) : 3- 10. https://perma.cc/2WFD-A2A7 KEY-WORDS Angiosperms family arrangement Summary: This paper provides, for herbarium cura- Gymnosperms Classification tors, the alphabetical lists of the recognized families Pteridophytes APG system in pteridophytes, gymnosperms and angiosperms Ferns PPG system with their phylogenetic classification numbers. Lycophytes phylogeny Herbarium MOTS-CLÉS Angiospermes rangement des familles Résumé : Cet article produit, pour les conservateurs Gymnospermes Classification d’herbier, les listes alphabétiques des familles recon- Ptéridophytes système APG nues pour les ptéridophytes, les gymnospermes et Fougères système PPG les angiospermes avec leurs numéros de classement Lycophytes phylogénie phylogénétique. Herbier Introduction These alphabetical lists have been established for the systems of A.-L de Jussieu, A.-P. de Can- The organization of herbarium collections con- dolle, Bentham & Hooker, etc. that are still used sists in arranging the specimens logically to in the management of historical herbaria find and reclassify them easily in the appro- whose original classification is voluntarily pre- priate storage units. In the vascular plant col- served. lections, commonly used methods are systema- Recent classification systems based on molecu- tic classification, alphabetical classification, or lar phylogenies have developed, and herbaria combinations of both.
    [Show full text]
  • Introduction to Common Native & Invasive Freshwater Plants in Alaska
    Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska Cover photographs by (top to bottom, left to right): Tara Chestnut/Hannah E. Anderson, Jamie Fenneman, Vanessa Morgan, Dana Visalli, Jamie Fenneman, Lynda K. Moore and Denny Lassuy. Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska This document is based on An Aquatic Plant Identification Manual for Washington’s Freshwater Plants, which was modified with permission from the Washington State Department of Ecology, by the Center for Lakes and Reservoirs at Portland State University for Alaska Department of Fish and Game US Fish & Wildlife Service - Coastal Program US Fish & Wildlife Service - Aquatic Invasive Species Program December 2009 TABLE OF CONTENTS TABLE OF CONTENTS Acknowledgments ............................................................................ x Introduction Overview ............................................................................. xvi How to Use This Manual .................................................... xvi Categories of Special Interest Imperiled, Rare and Uncommon Aquatic Species ..................... xx Indigenous Peoples Use of Aquatic Plants .............................. xxi Invasive Aquatic Plants Impacts ................................................................................. xxi Vectors ................................................................................. xxii Prevention Tips .................................................... xxii Early Detection and Reporting
    [Show full text]
  • ACTINIDIACEAE 1. ACTINIDIA Lindley, Nat. Syst. Bot., Ed. 2, 439
    ACTINIDIACEAE 猕猴桃科 mi hou tao ke Li Jianqiang (李建强)1, Li Xinwei (李新伟)1; Djaja Djendoel Soejarto2 Trees, shrubs, or woody vines. Leaves alternate, simple, shortly or long petiolate, not stipulate. Flowers bisexual or unisexual or plants polygamous or functionally dioecious, usually fascicled, cymose, or paniculate. Sepals (2 or 3 or)5, imbricate, rarely valvate. Petals (4 or)5, sometimes more, imbricate. Stamens 10 to numerous, distinct or adnate to base of petals, hypogynous; anthers 2- celled, versatile, dehiscing by apical pores or longitudinally. Ovary superior, disk absent, locules and carpels 3–5 or more; placentation axile; ovules anatropous with a single integument, 10 or more per locule; styles as many as carpels, distinct or connate (then only one style), generally persistent. Fruit a berry or leathery capsule. Seeds not arillate, with usually large embryos and abundant endosperm. Three genera and ca. 357 species: Asia and the Americas; three genera (one endemic) and 66 species (52 endemic) in China. Economically, kiwifruit (Actinidia chinensis var. deliciosa) is an important fruit, which originated in central China and is especially common along the Yangtze River (well known as yang-tao). Now, it is widely cultivated throughout the world. For additional information see the paper by X. W. Li, J. Q. Li, and D. D. Soejarto (Acta Phytotax. Sin. 45: 633–660. 2007). Liang Chou-fen, Chen Yong-chang & Wang Yu-sheng. 1984. Actinidiaceae (excluding Sladenia). In: Feng Kuo-mei, ed., Fl. Reipubl. Popularis Sin. 49(2): 195–301, 309–334. 1a. Trees or shrubs; flowers bisexual or plants functionally dioecious .................................................................................. 3. Saurauia 1b.
    [Show full text]
  • Download the Full Report Pdf, 2.9 MB
    VKM Report 2016:50 Assessment of the risks to Norwegian biodiversity from the import and keeping of aquarium and garden pond plants Opinion of the Panel on Alien Organisms and Trade in Endangered Species (CITES) of the Norwegian Scientific Committee for Food Safety Report from the Norwegian Scientific Committee for Food Safety (VKM) 2016:50 Assessment of the risks to Norwegian biodiversity from the import and keeping of aquarium and garden pond plants Opinion of the Panel on Alien Organisms and Trade in Endangered Species (CITES) of the Norwegian Scientific Committee for Food Safety 01.11.2016 ISBN: 00000-00000 Norwegian Scientific Committee for Food Safety (VKM) Po 4404 Nydalen N – 0403 Oslo Norway Phone: +47 21 62 28 00 Email: [email protected] www.vkm.no www.english.vkm.no Suggested citation: VKM (2016). Assessment of the risks to Norwegian biodiversity from the import and keeping of aquarium and garden pond plants. Scientific Opinion on the on Alien Organisms and Trade in Endangered species of the Norwegian Scientific Committee for Food Safety ISBN: 978-82-8259-240-6, Oslo, Norway. VKM Report 2016:50 Title: Assessment of the risks to Norwegian biodiversity from the import and keeping of aquarium and garden pond plants Authors preparing the draft opinion Hugo de Boer (chair), Maria G. Asmyhr (VKM staff), Hanne H. Grundt, Inga Kjersti Sjøtun, Hans K. Stenøien, Iris Stiers. Assessed and approved The opinion has been assessed and approved by Panel on Alien organisms and Trade in Endangered Species (CITES). Members of the panel are: Vigdis Vandvik (chair), Hugo de Boer, Jan Ove Gjershaug, Kjetil Hindar, Lawrence Kirkendall, Nina Elisabeth Nagy, Anders Nielsen, Eli K.
    [Show full text]
  • Acorus Calamus : an Overview
    Journal of Medicinal Plants Research Vol. 4(25), pp. 2740-2745, December Special Review, 2010 Available online at http://www.academicjournals.org/JMPR ISSN 1996-0875 ©2010 Academic Journals Review Acorus calamus : An overview R. Balakumbahan*, K. Rajamani and K. Kumanan Horticultural Research Station, TamilNadu Agricultural University, Pechiparai, 629161. Tamilnadu, India. Accepted 8 July, 2010 Acorus calamus (Sweet flag) is a wetland perennial monocot plant, in which the scented leaves and rhizomes have been traditionally used medicinally against different ailments like, fever, asthma, bronchitis, cough and mainly for digestive problems such as gas, bloating, colic, and poor digestive function. Number of active constituents and essential oil were identified and characterized from the leaves and rhizomes of sweet flag. An over view of the pharmacological activities and insecticidal activities are summarized here. Key words: Acorus calamus, Acorus gramineus , Acoraceae, active constituents, pharmacology. INTRODUCTION Mother earth has bestowed to the mankind and various Estimate reveals that the world trade in medicinal plants plants with healing ability for curing the ailments of and extracts industry was growing at a rate of 12 to 15% human being. This unique feature has been identified per annum. The export from India is to the tune of Rs 446 since pre historic times. The WHO has also estimated crores with the present growth rate of 7%. Acorus that 80% of the world population meets their primary calamus is a tall perennial wetland monocot plant from health care needs through traditional medicine only. the Acoraceae family. The scented leaves and rhizomes Medicinal plants are those plants possessing secondary of sweet flag have been traditionally used as a medicine metabolites and are potential sources of curative drugs and the dried and powdered rhizome has a spicy flavour with the very long list of chemicals and its curative nature.
    [Show full text]
  • Evolutionary History of Floral Key Innovations in Angiosperms Elisabeth Reyes
    Evolutionary history of floral key innovations in angiosperms Elisabeth Reyes To cite this version: Elisabeth Reyes. Evolutionary history of floral key innovations in angiosperms. Botanics. Université Paris Saclay (COmUE), 2016. English. NNT : 2016SACLS489. tel-01443353 HAL Id: tel-01443353 https://tel.archives-ouvertes.fr/tel-01443353 Submitted on 23 Jan 2017 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. NNT : 2016SACLS489 THESE DE DOCTORAT DE L’UNIVERSITE PARIS-SACLAY, préparée à l’Université Paris-Sud ÉCOLE DOCTORALE N° 567 Sciences du Végétal : du Gène à l’Ecosystème Spécialité de Doctorat : Biologie Par Mme Elisabeth Reyes Evolutionary history of floral key innovations in angiosperms Thèse présentée et soutenue à Orsay, le 13 décembre 2016 : Composition du Jury : M. Ronse de Craene, Louis Directeur de recherche aux Jardins Rapporteur Botaniques Royaux d’Édimbourg M. Forest, Félix Directeur de recherche aux Jardins Rapporteur Botaniques Royaux de Kew Mme. Damerval, Catherine Directrice de recherche au Moulon Président du jury M. Lowry, Porter Curateur en chef aux Jardins Examinateur Botaniques du Missouri M. Haevermans, Thomas Maître de conférences au MNHN Examinateur Mme. Nadot, Sophie Professeur à l’Université Paris-Sud Directeur de thèse M.
    [Show full text]
  • GENOME EVOLUTION in MONOCOTS a Dissertation
    GENOME EVOLUTION IN MONOCOTS A Dissertation Presented to The Faculty of the Graduate School At the University of Missouri In Partial Fulfillment Of the Requirements for the Degree Doctor of Philosophy By Kate L. Hertweck Dr. J. Chris Pires, Dissertation Advisor JULY 2011 The undersigned, appointed by the dean of the Graduate School, have examined the dissertation entitled GENOME EVOLUTION IN MONOCOTS Presented by Kate L. Hertweck A candidate for the degree of Doctor of Philosophy And hereby certify that, in their opinion, it is worthy of acceptance. Dr. J. Chris Pires Dr. Lori Eggert Dr. Candace Galen Dr. Rose‐Marie Muzika ACKNOWLEDGEMENTS I am indebted to many people for their assistance during the course of my graduate education. I would not have derived such a keen understanding of the learning process without the tutelage of Dr. Sandi Abell. Members of the Pires lab provided prolific support in improving lab techniques, computational analysis, greenhouse maintenance, and writing support. Team Monocot, including Dr. Mike Kinney, Dr. Roxi Steele, and Erica Wheeler were particularly helpful, but other lab members working on Brassicaceae (Dr. Zhiyong Xiong, Dr. Maqsood Rehman, Pat Edger, Tatiana Arias, Dustin Mayfield) all provided vital support as well. I am also grateful for the support of a high school student, Cady Anderson, and an undergraduate, Tori Docktor, for their assistance in laboratory procedures. Many people, scientist and otherwise, helped with field collections: Dr. Travis Columbus, Hester Bell, Doug and Judy McGoon, Julie Ketner, Katy Klymus, and William Alexander. Many thanks to Barb Sonderman for taking care of my greenhouse collection of many odd plants brought back from the field.
    [Show full text]
  • Biogeography and Diversification of Brassicales
    Molecular Phylogenetics and Evolution 99 (2016) 204–224 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Biogeography and diversification of Brassicales: A 103 million year tale ⇑ Warren M. Cardinal-McTeague a,1, Kenneth J. Sytsma b, Jocelyn C. Hall a, a Department of Biological Sciences, University of Alberta, Edmonton, Alberta T6G 2E9, Canada b Department of Botany, University of Wisconsin, Madison, WI 53706, USA article info abstract Article history: Brassicales is a diverse order perhaps most famous because it houses Brassicaceae and, its premier mem- Received 22 July 2015 ber, Arabidopsis thaliana. This widely distributed and species-rich lineage has been overlooked as a Revised 24 February 2016 promising system to investigate patterns of disjunct distributions and diversification rates. We analyzed Accepted 25 February 2016 plastid and mitochondrial sequence data from five gene regions (>8000 bp) across 151 taxa to: (1) Available online 15 March 2016 produce a chronogram for major lineages in Brassicales, including Brassicaceae and Arabidopsis, based on greater taxon sampling across the order and previously overlooked fossil evidence, (2) examine Keywords: biogeographical ancestral range estimations and disjunct distributions in BioGeoBEARS, and (3) determine Arabidopsis thaliana where shifts in species diversification occur using BAMM. The evolution and radiation of the Brassicales BAMM BEAST began 103 Mya and was linked to a series of inter-continental vicariant, long-distance dispersal, and land BioGeoBEARS bridge migration events. North America appears to be a significant area for early stem lineages in the Brassicaceae order. Shifts to Australia then African are evident at nodes near the core Brassicales, which diverged Cleomaceae 68.5 Mya (HPD = 75.6–62.0).
    [Show full text]