Biosystematic Studies in Loganiaceae (Series 4): Phytomorphological Characterization in Relation to Intraspecific Delimitation A
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Flowering Plants Eudicots Apiales, Gentianales (Except Rubiaceae)
Edited by K. Kubitzki Volume XV Flowering Plants Eudicots Apiales, Gentianales (except Rubiaceae) Joachim W. Kadereit · Volker Bittrich (Eds.) THE FAMILIES AND GENERA OF VASCULAR PLANTS Edited by K. Kubitzki For further volumes see list at the end of the book and: http://www.springer.com/series/1306 The Families and Genera of Vascular Plants Edited by K. Kubitzki Flowering Plants Á Eudicots XV Apiales, Gentianales (except Rubiaceae) Volume Editors: Joachim W. Kadereit • Volker Bittrich With 85 Figures Editors Joachim W. Kadereit Volker Bittrich Johannes Gutenberg Campinas Universita¨t Mainz Brazil Mainz Germany Series Editor Prof. Dr. Klaus Kubitzki Universita¨t Hamburg Biozentrum Klein-Flottbek und Botanischer Garten 22609 Hamburg Germany The Families and Genera of Vascular Plants ISBN 978-3-319-93604-8 ISBN 978-3-319-93605-5 (eBook) https://doi.org/10.1007/978-3-319-93605-5 Library of Congress Control Number: 2018961008 # Springer International Publishing AG, part of Springer Nature 2018 This work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfilms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed. The use of general descriptive names, registered names, trademarks, service marks, etc. in this publication does not imply, even in the absence of a specific statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use. -
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. -
Temporal and Spatial Origin of Gesneriaceae in the New World Inferred from Plastid DNA Sequences
bs_bs_banner Botanical Journal of the Linnean Society, 2013, 171, 61–79. With 3 figures Temporal and spatial origin of Gesneriaceae in the New World inferred from plastid DNA sequences MATHIEU PERRET1*, ALAIN CHAUTEMS1, ANDRÉA ONOFRE DE ARAUJO2 and NICOLAS SALAMIN3,4 1Conservatoire et Jardin botaniques de la Ville de Genève, Ch. de l’Impératrice 1, CH-1292 Chambésy, Switzerland 2Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, Rua Santa Adélia, 166, Bairro Bangu, Santo André, Brazil 3Department of Ecology and Evolution, University of Lausanne, CH-1015 Lausanne, Switzerland 4Swiss Institute of Bioinformatics, Quartier Sorge, CH-1015 Lausanne, Switzerland Received 15 December 2011; revised 3 July 2012; accepted for publication 18 August 2012 Gesneriaceae are represented in the New World (NW) by a major clade (c. 1000 species) currently recognized as subfamily Gesnerioideae. Radiation of this group occurred in all biomes of tropical America and was accompanied by extensive phenotypic and ecological diversification. Here we performed phylogenetic analyses using DNA sequences from three plastid loci to reconstruct the evolutionary history of Gesnerioideae and to investigate its relationship with other lineages of Gesneriaceae and Lamiales. Our molecular data confirm the inclusion of the South Pacific Coronanthereae and the Old World (OW) monotypic genus Titanotrichum in Gesnerioideae and the sister-group relationship of this subfamily to the rest of the OW Gesneriaceae. Calceolariaceae and the NW genera Peltanthera and Sanango appeared successively sister to Gesneriaceae, whereas Cubitanthus, which has been previously assigned to Gesneriaceae, is shown to be related to Linderniaceae. Based on molecular dating and biogeographical reconstruction analyses, we suggest that ancestors of Gesneriaceae originated in South America during the Late Cretaceous. -
A New Formal Classification of Gesneriaceae Is Proposed
Selbyana 31(2): 68–94. 2013. ANEW FORMAL CLASSIFICATION OF GESNERIACEAE ANTON WEBER* Department of Structural and Functional Botany, Faculty of Biodiversity, University of Vienna, A-1030 Vienna, Austria. Email: [email protected] JOHN L. CLARK Department of Biological Sciences, The University of Alabama, Tuscaloosa, AL 35487, USA. MICHAEL MO¨ LLER Royal Botanic Garden Edinburgh, Edinburgh EH3 5LR, Scotland, U.K. ABSTRACT. A new formal classification of Gesneriaceae is proposed. It is the first detailed and overall classification of the family that is essentially based on molecular phylogenetic studies. Three subfamilies are recognized: Sanangoideae (monospecific with Sanango racemosum), Gesnerioideae and Didymocarpoideae. As to recent molecular data, Sanango/Sanangoideae (New World) is sister to Gesnerioideae + Didymocarpoideae. Its inclusion in the Gesneriaceae amends the traditional concept of the family and makes the family distinctly older. Subfam. Gesnerioideae (New World, if not stated otherwise with the tribes) is subdivided into five tribes: Titanotricheae (monospecific, East Asia), Napeantheae (monogeneric), Beslerieae (with two subtribes: Besleriinae and Anetanthinae), Coronanthereae (with three subtribes: Coronantherinae, Mitrariinae and Negriinae; southern hemisphere), and Gesnerieae [with five subtribes: Gesneriinae, Gloxiniinae, Columneinae (5the traditional Episcieae), Sphaerorrhizinae (5the traditional Sphaerorhizeae, monogeneric), and Ligeriinae (5the traditional Sinningieae)]. In the Didymocarpoideae (almost exclusively -
Chapter One 1.0 Introduction and Background to The
CHAPTER ONE 1.0 INTRODUCTION AND BACKGROUND TO THE STUDY Loganiaceae is a family of flowering plants classified in the Order Gentianales (Bendre, 1975). The family was first suggested by Robert Brown in 1814 and validly published by von Martius in 1827 (Nicholas and Baijnath, 1994). Members habits are in form of trees, shrubs, woody climbers and herbs. Some are epiphytes while some members are furnished with spines or tendrils (Bendre, 1975). They are distributed mainly in the tropics, subtropics and a few in temperate regions (Backlund et al., 2000). Earlier treatments of the family have included up to 30 genera, 600 species (Leeuwenberg and Leenhouts, 1980; Mabberley, 1997) but were later reduced to 400 species in 15 genera, with some species extending into temperate Australia and North America (Struwe et al., 1994; Dunlop, 1996; Backlund and Bremer, 1998). Morphological studies have demonstrated that this broadly defined Loganiaceae was a polyphyletic assemblage and numerous genera have been removed from it to other families (sometimes to other Orders), e.g. Gentianaceae, Gelsemiaceae, Plocospermataceae, Tetrachondraceae, Buddlejaceae, and Gesneriaceae (Backlund and Bremer, 1998; Backlund et al., 2000). The family has undergone numerous revisions that have expanded and contracted its circumscription, ranging from one genus at its smallest (Takhtajan, 1997; Smith et al., 1997) to 30 at its largest (Leeuwenberg and Leenhouts, 1980). One of the current infrafamilial classifications contains four tribes: Antonieae Endl., Loganieae Endl., Spigelieae Dum. (monotypic), and Strychneae Dum. (Struwe et al., 1994). The tribes Loganieae and Antonieae are supported by molecular data, but Strychneae is not (Backlund et al., 2000). -
The Disintegration of the Scrophulariaceae and the Biological Control of Buddleja Davidii
The disintegration of the Scrophulariaceae and the biological control of Buddleja davidii M.K. Kay,1 B. Gresham,1 R.L. Hill2 and X. Zhang3 Summary The woody shrub buddleia, Buddleja davidii Franchet, is an escalating weed problem for a number of resource managers in temperate regions. The plant’s taxonomic isolation within the Buddlejaceae was seen as beneficial for its biological control in both Europe and New Zealand. However, the re- cent revision of the Scrophulariaceae has returned Buddleja L. to the Scrophulariaceae sensu stricto. Although this proved of little consequence to the New Zealand situation, it may well compromise Eu- ropean biocontrol considerations. Host-specificity tests concluded that the biocontrol agent, Cleopus japonicus Wingelmüller (Coleoptera, Curculionidae), was safe to release in New Zealand. This leaf- feeding weevil proved capable of utilising a few non-target plants within the same clade as Buddleja but exhibited increased mortality and development times. The recent release of the weevil in New Zealand offers an opportunity to safely assess the risk of this agent to European species belonging to the Scrophulariaceae. Keywords: Cleopus, Buddleja, taxonomic revision, phylogeny. Introduction there is no significant soil seed bank. The seed germi- nates almost immediately, and the density and rapid There are approximately 90 species of Buddleja L. early growth of buddleia seedlings suppresses other indigenous to the Americas, Asia and Africa (Leeu- pioneer species (Smale, 1990). wenberg, 1979), and a number have become natural- As a naturalized species, buddleia is a shade-intolerant ized outside their native ranges (Holm et al., 1979). colonizer of urban wastelands, riparian margins and Buddleia, Buddleja davidii Franchet, in particular, is an other disturbed sites, where it may displace indigenous escalating problem for resource managers in temperate species, alter nutrient dynamics and impede access regions and has been identified as a target for classi- (Smale, 1990; Bellingham et al., 2005). -
THE LOGANIACEAE of AFRICA XVIII Buddleja L. II Revision of the African and Asiatic Species
582.935.4(5) 582.935.4(6) MEDEDELINGEN LANDBOUWHOGESCHOOL WAGENINGEN • NEDERLAND • 79-6 (1979) THE LOGANIACEAE OF AFRICA XVIII Buddleja L. II Revision of the African and Asiatic species A. J. M. LEEUWENBERG Laboratory of Plant Taxonomy and Plant Geography, Agricultural University, Wageningen, The Netherlands Received 24-X-1978 Date of publication 5-IX-1979 H. VEENMAN & ZONEN B.V. -WAGENINGEN- 1979 CONTENTS page INTRODUCTION 1 GENERAL PART 2 History of the genus 2 Geographical distribution and ecology 2 Relationship to other genera 3 TAXONOMIC PART 5 The genus Buddleja 5 Sectional arrangement 7 Discussion of the relationship ofth e sections and of their delimitation 9 Key to the species represented in Africa 11 Key to the species indigenous in Asia 14 Alphabetical list of the sections accepted and species revised here B. acuminata Poir 17 albiflora Hemsl 86 alternifolia Maxim. 89 asiatica Lour 92 auriculata Benth. 20 australis Veil 24 axillaris Willd. ex Roem. et Schult 27 bhutanica Yamazaki 97 brachystachya Diels 97 section Buddleja 7 Candida Dunn 101 section Chilianthus (Burch.) Leeuwenberg 7 colvilei Hook. f. et Thorns. 103 cordataH.B.K 30 crispa Benth 105 curviflora Hook, et Arn Ill cuspidata Bak 35 davidii Franch. 113 delavayi Gagnep. 119 dysophylla (Benth.) Radlk. 37 fallowiana Balf. f. et W. W. Smith 121 forrestii Diels 124 fragifera Leeuwenberg 41 fusca Bak 43 globosa Hope 45 glomerata Wendl. f. 49 indica Lam. 51 japonica Hemsl. 127 lindleyana Fortune 129 loricata Leeuwenberg 56 macrostachya Benth 133 madagascariensis Lam 59 myriantha Diels 136 section Neemda Benth 7 section Nicodemia (Tenore) Leeuwenberg 9 nivea Duthie 137 officinalis Maxim 140 paniculata Wall 142 polystachya Fresen. -
The Families and Genera of Vascular Plants
THE FAMILIES AND GENERA OF VASCULAR PLANTS Edited by K. Kubitzki For further volumes see list at the end of the book and: http://www.springer.com/series/1306 The Families and Genera of Vascular Plants Edited by K. Kubitzki Flowering Plants Á Eudicots XV Apiales, Gentianales (except Rubiaceae) Volume Editors: Joachim W. Kadereit • Volker Bittrich With 85 Figures Editors Joachim W. Kadereit Volker Bittrich Johannes Gutenberg Campinas Universita¨t Mainz Brazil Mainz Germany Series Editor Prof. Dr. Klaus Kubitzki Universita¨t Hamburg Biozentrum Klein-Flottbek und Botanischer Garten 22609 Hamburg Germany The Families and Genera of Vascular Plants ISBN 978-3-319-93604-8 ISBN 978-3-319-93605-5 (eBook) https://doi.org/10.1007/978-3-319-93605-5 Library of Congress Control Number: 2018961008 # Springer International Publishing AG, part of Springer Nature 2018 This work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfilms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed. The use of general descriptive names, registered names, trademarks, service marks, etc. in this publication does not imply, even in the absence of a specific statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use. The publisher, the authors and the editors are safe to assume that the advice and information in this book are believed to be true and accurate at the date of publication. -
A Survey of Tricolpate (Eudicot) Phylogenetic Relationships1
American Journal of Botany 91(10): 1627±1644. 2004. A SURVEY OF TRICOLPATE (EUDICOT) PHYLOGENETIC RELATIONSHIPS1 WALTER S. JUDD2,4 AND RICHARD G. OLMSTEAD3 2Department of Botany, University of Florida, Gainesville, Florida 32611 USA; and 3Department of Biology, University of Washington, Seattle, Washington 98195 USA The phylogenetic structure of the tricolpate clade (or eudicots) is presented through a survey of their major subclades, each of which is brie¯y characterized. The tricolpate clade was ®rst recognized in 1989 and has received extensive phylogenetic study. Its major subclades, recognized at ordinal and familial ranks, are now apparent. Ordinal and many other suprafamilial clades are brie¯y diag- nosed, i.e., the putative phenotypic synapomorphies for each major clade of tricolpates are listed, and the support for the monophyly of each clade is assessed, mainly through citation of the pertinent molecular phylogenetic literature. The classi®cation of the Angiosperm Phylogeny Group (APG II) expresses the current state of our knowledge of phylogenetic relationships among tricolpates, and many of the major tricolpate clades can be diagnosed morphologically. Key words: angiosperms; eudicots; tricolpates. Angiosperms traditionally have been divided into two pri- 1992a; Chase et al., 1993; Doyle et al., 1994; Soltis et al., mary groups based on the presence of a single cotyledon 1997, 2000, 2003; KaÈllersjoÈ et al., 1998; Nandi et al., 1998; (monocotyledons, monocots) or two cotyledons (dicotyledons, Hoot et al., 1999; Savolainen et al., 2000a, b; Hilu et al., 2003; dicots). A series of additional diagnostic traits made this di- Zanis et al., 2003; Kim et al., 2004). This clade was ®rst called vision useful and has accounted for the long recognition of the tricolpates (Donoghue and Doyle, 1989), but the name these groups in ¯owering plant classi®cations. -
Butterfly Bush)
Bot. Rev. DOI 10.1007/s12229-009-9033-0 The Invasive Buddleja davidii (Butterfly Bush) Nita G. Tallent-Halsell1,2,4 & Michael S. Watt3 1 Landscape Ecology Branch, US Environmental Protection Agency, 944 E. Harmon Ave., Las Vegas, NV 89119, USA 2 University of Nevada, Las Vegas, 4505 S. Maryland Parkway, Las Vegas, NV 89154, USA 3 Scion, P.O. Box 29237, Christchurch, New Zealand 4 Author for Correspondence; e-mail: [email protected] # The New York Botanical Garden 2009 Abstract Buddleja davidii Franchet (Synonym. Buddleia davidii; common name butterfly bush) is a perennial, semi-deciduous, multi-stemmed shrub that is resident in gardens and disturbed areas. Since its introduction to the United Kingdom from China in the late 1800s, B. davidii has become an important component in horticulture and human culture. Despite its popularity as a landscape plant, B. davidii is considered problematic because of its ability to naturalize outside of gardens and rapidly invade and dominate disturbed natural areas across a wide range of physical conditions. The primary goal of this paper is to synthesize what is known about B. davidii in order to understand the impacts caused by the continued presence of B. davidii in gardens and natural landscapes. We also address management of B. davidii and discuss the repercussions of management strategies and policies currently implemented to protect or remove B. davidii from natural ecosystems. Zusammenfassung Buddleja davidii Franchet (Synonym Buddleia davidii, umgang- sprachlich “Schmetterlingsflieder”) ist ein ausdauernder, halb-immergruener, mehr- staemmiger Busch welcher in Gaerten und auf Umbruchflaechen gedeiht. Seit seiner Einfuehrung in die UK aus China im spaeten 19. -
Serikali Ya Mapinduzi Zanzibar Care Tanzania And
SERIKALI YA MAPINDUZI ZANZIBAR CARE TANZANIA AND DEPARTMENT OF COMMERCIAL CROPS, FRUITS AND FORESTRY NGEZI – VUMAWIMBI FOREST RESERVES BIODIVERSITY INVENTORY REPORT PREPARED BY C. L. NAHONYO, L. B. MWASUMBI, C. A. MSUYA, C.A. MASAO, T. B. SUYA AND C. SHING’WENDA DEPARTMENT OF ZOOLOGY AND MARINE BIOLOGY UNIVERSITY OF DAR ES SALAAM P. O. BOX 35064 DAR ES SALAAM, TANZANIA [email protected] JULY 2005 Table of Contents Item Page Title………………………………………………………….……………………... i Table of Contents………………………………………………………………….. ii List of Tables………………………………………………………………………. iv List of Figures……………………………………………………………………… v List of Maps………………………………………………………………………... v List of Appendices…………………………………………………………………. vi Acknowledgements………………………………………………………………… vii Map showing position of Pemba relative to Tanzania mainland……………….….. viii Map of Zanzibar showing position of Ngezi –Vumawimbi Forest Reserves.……... ix Executive Summary………………………………………………………………... x 1.0 INTRODUCTION……………………………………………………………... 1 1.1 Overview of Tanzania biodiversity………………………………………… 2 1.2 Brief history of Ngezi –Vumawimbi study area…………………………… 3 1.2.1 History of Ngezi forest………………………………………………… 3 2.0 THE SURVEY AREA…………………………………………………………. 5 2.1 Location……………………………………………………………………. 5 2.2 Scope……………………………………………………………………….. 5 2.3 Accessibility………………………………………………………………... 5 2.4 Topography………………………………………………………………… 5 2.5 Geology and hydrology...………………………………………………….. 6 2.6 Soils………………………………………………………………………... 6 2.7 Climate……………………………………………………………………... 6 2.8 Vegetation…………………………………………………………………. -
Bremer Et Al. 2001
Plant Syst. Evol. 229: 137±169 <2001) A phylogenetic analysis of 100+ genera and 50+ families of euasterids based on morphological and molecular data with notes on possible higher level morphological synapomorphies K. Bremer1, A. Backlund2, B. Sennblad3, U. Swenson4, K. Andreasen5, M. Hjertson1, J. Lundberg1, M. Backlund1, and B. Bremer1 1Department of Systematic Botany, Evolutionary Biology Centre, Uppsala University, Uppsala, Sweden 2Department of Medicinal Chemistry, Uppsala University, Uppsala, Sweden 3Stockholm Bioinformatics Center, Stockholm University, Stockholm, Sweden 4Department of Botany, University of Stockholm, Stockholm, Sweden 5Molecular Systematics Laboratory, Swedish Museum of Natural History, Stockholm, Sweden Received August 28, 2000 Accepted August 7, 2001 Abstract. A data matrix of 143 morphological and epigynous ¯owers, ``late sympetaly'' with distinct chemical characters for 142 genera of euasterids petal primordia, free stamen ®laments, and indehi- according to the APG system was compiled and scent fruits. It is unclear which of these characters complemented with rbcL and ndhF sequences for represent synapomorphies and symplesiomorphies most of the genera. The data were subjected to for the two groups, respectively, and there are parsimony analysis and support was assessed by numerous expections to be interpreted as reversals bootstrapping. Strict consensus trees from analyses and parallelisms. of morphology alone and morphology + rbcL+ ndhF are presented. The morphological data re- Key words: Angiosperms, asterids, euasterids, cover several groups supported by molecular data Asteridae, Apiales, Aquifoliales, Asterales, but at the level of orders and above relationships Dipsacales, Garryales, Gentianales, Lamiales, are only super®cially in agreement with molecular Solanales, Adoxaceae. Cladistics, phylogeny, studies. The analyses provide support for mono- morphology, rbcL, ndhF.