Thunbergia Fragrans1
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ORNAMENTAL GARDEN PLANTS of the GUIANAS: an Historical Perspective of Selected Garden Plants from Guyana, Surinam and French Guiana
f ORNAMENTAL GARDEN PLANTS OF THE GUIANAS: An Historical Perspective of Selected Garden Plants from Guyana, Surinam and French Guiana Vf•-L - - •• -> 3H. .. h’ - — - ' - - V ' " " - 1« 7-. .. -JZ = IS^ X : TST~ .isf *“**2-rt * * , ' . / * 1 f f r m f l r l. Robert A. DeFilipps D e p a r t m e n t o f B o t a n y Smithsonian Institution, Washington, D.C. \ 1 9 9 2 ORNAMENTAL GARDEN PLANTS OF THE GUIANAS Table of Contents I. Map of the Guianas II. Introduction 1 III. Basic Bibliography 14 IV. Acknowledgements 17 V. Maps of Guyana, Surinam and French Guiana VI. Ornamental Garden Plants of the Guianas Gymnosperms 19 Dicotyledons 24 Monocotyledons 205 VII. Title Page, Maps and Plates Credits 319 VIII. Illustration Credits 321 IX. Common Names Index 345 X. Scientific Names Index 353 XI. Endpiece ORNAMENTAL GARDEN PLANTS OF THE GUIANAS Introduction I. Historical Setting of the Guianan Plant Heritage The Guianas are embedded high in the green shoulder of northern South America, an area once known as the "Wild Coast". They are the only non-Latin American countries in South America, and are situated just north of the Equator in a configuration with the Amazon River of Brazil to the south and the Orinoco River of Venezuela to the west. The three Guianas comprise, from west to east, the countries of Guyana (area: 83,000 square miles; capital: Georgetown), Surinam (area: 63, 037 square miles; capital: Paramaribo) and French Guiana (area: 34, 740 square miles; capital: Cayenne). Perhaps the earliest physical contact between Europeans and the present-day Guianas occurred in 1500 when the Spanish navigator Vincente Yanez Pinzon, after discovering the Amazon River, sailed northwest and entered the Oyapock River, which is now the eastern boundary of French Guiana. -
Thunbergia Species Thunbergia Spp
Fact sheet DECLARED CLASS 1 AND 2 PEST PLANT Thunbergia species Thunbergia spp. The four species of thunbergia declared under the Land T. grandiflora is the most widespread pest species, having Protection (Pest and Stock Route Management) Act 2002 been used as a garden ornamental for its attractive large in Queensland are: leaves and hanging groups of large, pale lavender flowers. • Thunbergia laurifolia—laurel clockvine (Class 1) While other species of thunbergia (black-eyed susan, • Thunbergia annua (Class 1) scarlet clock vine, golden glory vine, lady’s slipper) are not declared, they are not recommended for planting because • Thunbergia fragrans (Class 1) of their potential to spread into surrounding bush. • Thunbergia grandiflora—blue trumpet vine or blue sky vine (Class 2). PP23 September 2011 T. arnhemica is the only native species and occurs in northern parts of Queensland, the Northern Territory and Western Australia (can be confused with T. fragrans). Thunbergia species are a major threat to remnant vegetation in the wet tropics. In the past T. grandiflora and T. laurifolia were promoted and sold in Queensland as attractive garden plants, and both became widespread in Queensland gardens. These vigorous plants soon escaped into native bushland and began causing considerable environmental damage. The plant climbs and blankets native vegetation, with the weight of the vine often pulling down mature trees. Smothered vegetation also has dramatically reduced light levels to lower layers of vegetation, drastically limiting Thunbergia laurifolia infestation natural growth and killing many native plants. Large tubers degrade creek and river banks and make destruction of Other species of thunbergia the pest difficult. -
ACANTHACEAE 爵床科 Jue Chuang Ke Hu Jiaqi (胡嘉琪 Hu Chia-Chi)1, Deng Yunfei (邓云飞)2; John R
ACANTHACEAE 爵床科 jue chuang ke Hu Jiaqi (胡嘉琪 Hu Chia-chi)1, Deng Yunfei (邓云飞)2; John R. I. Wood3, Thomas F. Daniel4 Prostrate, erect, or rarely climbing herbs (annual or perennial), subshrubs, shrubs, or rarely small trees, usually with cystoliths (except in following Chinese genera: Acanthus, Blepharis, Nelsonia, Ophiorrhiziphyllon, Staurogyne, and Thunbergia), isophyllous (leaf pairs of equal size at each node) or anisophyllous (leaf pairs of unequal size at each node). Branches decussate, terete to angular in cross-section, nodes often swollen, sometimes spinose with spines derived from reduced leaves, bracts, and/or bracteoles. Stipules absent. Leaves opposite [rarely alternate or whorled]; leaf blade margin entire, sinuate, crenate, dentate, or rarely pinnatifid. Inflo- rescences terminal or axillary spikes, racemes, panicles, or dense clusters, rarely of solitary flowers; bracts 1 per flower or dichasial cluster, large and brightly colored or minute and green, sometimes becoming spinose; bracteoles present or rarely absent, usually 2 per flower. Flowers sessile or pedicellate, bisexual, zygomorphic to subactinomorphic. Calyx synsepalous (at least basally), usually 4- or 5-lobed, rarely (Thunbergia) reduced to an entire cupular ring or 10–20-lobed. Corolla sympetalous, sometimes resupinate 180º by twisting of corolla tube; tube cylindric or funnelform; limb subactinomorphic (i.e., subequally 5-lobed) or zygomorphic (either 2- lipped with upper lip subentire to 2-lobed and lower lip 3-lobed, or rarely 1-lipped with 3 lobes); lobes ascending or descending cochlear, quincuncial, contorted, or open in bud. Stamens epipetalous, included in or exserted from corolla tube, 2 or 4 and didyna- mous; filaments distinct, connate in pairs, or monadelphous basally via a sheath (Strobilanthes); anthers with 1 or 2 thecae; thecae parallel to perpendicular, equally inserted to superposed, spherical to linear, base muticous or spurred, usually longitudinally dehis- cent; staminodes 0–3, consisting of minute projections or sterile filaments. -
Agneta Julia Borg
Evolutionary relationships in Thunbergioideae and other early branching lineages of Acanthac e a e Agneta Julia Borg Evolutionary relationships in Thunbergioideae and other early branching lineages of Acanthaceae Agneta Julia Borg ©Agneta Julia Borg, Stockholm 2012 Cover illustration: From top left, Mendoncia retusa, Thunbergia convolvulifolia , Pseudocalyx saccatus, Crossandra strobilifera, Avicennia bicolor, Elytraria marginata. Photos: Agneta Julia Borg and Jürg Schönenberger. ISBN 978-91-7447-445-9 Printed in Sweden by Universitetsservice US-AB, Stockholm 2012 Distributor: Department of Botany, Stockholm University Academic dissertation for the degree of Doctor of Philosophy in Plant Sys- tematics presented at Stockholm University 2012 Abstract Borg, A.J. 2012. Evolutionary relationships in Thunbergioideae and other early branching lineages of Acanthaceae. Acanthaceae as circumscribed today consists of the three subfamilies Acan- thoideae (Acanthaceae sensu stricto), Thunbergioideae and Nelsonioideae, plus the genus Avicennia. Due to the morphological dissimilarities of Thun- bergioideae and Nelsonioideae, the delimitation of the family has been con- troversial. The mangrove genus Avicennia was only recently associated with Acanthaceae for the first time, based on molecular evidence, but without morphological support. In this thesis, phylogenetic analyses of nuclear and chloroplast DNA sequences were used to test the monophyly and exact posi- tions of Thunbergioideae and Nelsonioideae, and to infer detailed phyloge- netic relationships within these subfamilies and among major lineages of Acanthaceae. Floral structure and development were comparatively studied in Avicennia and other Acanthaceae using scanning electron microscopy and stereo microscopy. Phylogenetic analyses strongly support monophyly of Thunbergioideae and Nelsonioideae, and place the latter clade with strong support as sister to all other plants treated as Acanthaceae. -
Lamiales – Synoptical Classification Vers
Lamiales – Synoptical classification vers. 2.6.2 (in prog.) Updated: 12 April, 2016 A Synoptical Classification of the Lamiales Version 2.6.2 (This is a working document) Compiled by Richard Olmstead With the help of: D. Albach, P. Beardsley, D. Bedigian, B. Bremer, P. Cantino, J. Chau, J. L. Clark, B. Drew, P. Garnock- Jones, S. Grose (Heydler), R. Harley, H.-D. Ihlenfeldt, B. Li, L. Lohmann, S. Mathews, L. McDade, K. Müller, E. Norman, N. O’Leary, B. Oxelman, J. Reveal, R. Scotland, J. Smith, D. Tank, E. Tripp, S. Wagstaff, E. Wallander, A. Weber, A. Wolfe, A. Wortley, N. Young, M. Zjhra, and many others [estimated 25 families, 1041 genera, and ca. 21,878 species in Lamiales] The goal of this project is to produce a working infraordinal classification of the Lamiales to genus with information on distribution and species richness. All recognized taxa will be clades; adherence to Linnaean ranks is optional. Synonymy is very incomplete (comprehensive synonymy is not a goal of the project, but could be incorporated). Although I anticipate producing a publishable version of this classification at a future date, my near- term goal is to produce a web-accessible version, which will be available to the public and which will be updated regularly through input from systematists familiar with taxa within the Lamiales. For further information on the project and to provide information for future versions, please contact R. Olmstead via email at [email protected], or by regular mail at: Department of Biology, Box 355325, University of Washington, Seattle WA 98195, USA. -
The Linderniaceae and Gratiolaceae Are Further Lineages Distinct from the Scrophulariaceae (Lamiales)
Research Paper 1 The Linderniaceae and Gratiolaceae are further Lineages Distinct from the Scrophulariaceae (Lamiales) R. Rahmanzadeh1, K. Müller2, E. Fischer3, D. Bartels1, and T. Borsch2 1 Institut für Molekulare Physiologie und Biotechnologie der Pflanzen, Universität Bonn, Kirschallee 1, 53115 Bonn, Germany 2 Nees-Institut für Biodiversität der Pflanzen, Universität Bonn, Meckenheimer Allee 170, 53115 Bonn, Germany 3 Institut für Integrierte Naturwissenschaften ± Biologie, Universität Koblenz-Landau, Universitätsstraûe 1, 56070 Koblenz, Germany Received: July 14, 2004; Accepted: September 22, 2004 Abstract: The Lamiales are one of the largest orders of angio- Traditionally, Craterostigma, Lindernia and their relatives have sperms, with about 22000 species. The Scrophulariaceae, as been treated as members of the family Scrophulariaceae in the one of their most important families, has recently been shown order Lamiales (e.g., Takhtajan,1997). Although it is well estab- to be polyphyletic. As a consequence, this family was re-classi- lished that the Plocospermataceae and Oleaceae are their first fied and several groups of former scrophulariaceous genera branching families (Bremer et al., 2002; Hilu et al., 2003; Soltis now belong to different families, such as the Calceolariaceae, et al., 2000), little is known about the evolutionary diversifica- Plantaginaceae, or Phrymaceae. In the present study, relation- tion of most of the orders diversity. The Lamiales branching ships of the genera Craterostigma, Lindernia and its allies, hith- above the Plocospermataceae and Oleaceae are called ªcore erto classified within the Scrophulariaceae, were analyzed. Se- Lamialesº in the following text. The most recent classification quences of the chloroplast trnK intron and the matK gene by the Angiosperm Phylogeny Group (APG2, 2003) recognizes (~ 2.5 kb) were generated for representatives of all major line- 20 families. -
Flora of China (1994-2013) in English, More Than 100 New Taxa of Chinese Plants Are Still Being Published Each Year
This Book is Sponsored by Shanghai Chenshan Botanical Garden 上海辰山植物园 Shanghai Chenshan Plant Science Research Center, Chinese Academy of Sciences 中国科学院上海辰山植物科学研究中心 Special Fund for Scientific Research of Shanghai Landscaping & City Appearance Administrative Bureau (G182415) 上海市绿化和市容管理局科研专项 (G182415) National Specimen Information Infrastructure, 2018 Special Funds 中国国家标本平台 2018 年度专项 Shanghai Sailing Program (14YF1413800) 上海市青年科技英才扬帆计划 (14YF1413800) Chinese Plant Names Index 2000-2009 DU Cheng & MA Jin-shuang Chinese Plant Names Index 2000-2009 中国植物名称索引 2000-2009 DU Cheng & MA Jin-shuang Abstract The first two volumes of the Chinese Plant Names Index (CPNI) cover the years 2000 through 2009, with entries 1 through 5,516, and 2010 through 2017, with entries 5,517 through 10,795. A unique entry is generated for the specific name of each taxon in a specific publication. Taxonomic treatments cover all novelties at the rank of family, genus, species, subspecies, variety, form and named hybrid taxa, new name changes (new combinations and new names), new records, new synonyms and new typifications for vascular plants reported or recorded from China. Detailed information on the place of publication, including author, publication name, year of publication, volume, issue, and page number, are given in detail. Type specimens and collections information for the taxa and their distribution in China, as well as worldwide, are also provided. The bibliographies were compiled from 182 journals and 138 monographs or books published worldwide. In addition, more than 400 herbaria preserve type specimens of Chinese plants are also listed as an appendix. This book can be used as a basic material for Chinese vascular plant taxonomy, and as a reference for researchers in biodiversity research, environmental protection, forestry and medicinal botany. -
Thunbergia Thunbergia Grandiflora (Syn
Restricted invasive plant Lantana BlueLantana camara thunbergia Thunbergia grandiflora (syn. Thunbergia laurifolia) Blue thunbergia was promoted and sold in Queensland as Large tubers degrade creek and river banks and make an attractive garden plant, and both became widespread destruction of blue thunbergia difficult. in Queensland gardens. These vigorous plants soon In garden situations, it will also quickly spread and the escaped into native bushland and began causing large tubers may cause damage to paths, fences and considerable environmental damage. foundations. Other ornamental species of thunbergia The plant climbs and blankets native vegetation, with (black-eyed Susan, scarlet clock vine, golden glory vine, the weight of the vine often pulling down mature trees. lady’s slipper) are not as invasive, they are also not Smothered vegetation also has dramatically reduced light recommended for planting because of their potential to levels to lower layers of vegetation, drastically limiting spread into sourrounding bush land. natural growth and killing many native plants. Thunbergia species are a major threat to remnant Habitat and distribution vegetation in the wet tropics. Native to northern India and tropical Africa, and grow best Legal requirements in frost-free locations. Infestations of blue thunbergia are patchy and are mostly scattered along coastal streams Blue thunbergia is a restricted category 3 invasive plant from the Tully River to the Daintree. Areas of acute under the Biosecurity Act 2014. It must not be given away, infestation are the Mulgrave River, the Johnstone River and sold, or released into the environment. lower Mossman River. Some specimens collected in Queensland were previously identified asThunbergia laurifolia. -
Lianas No Neotropico
Lianas no Neotrópico parte 7 Dr. Pedro Acevedo R. Museum of Natural History Smithsonian Institution Washington, DC 2018 Asterids: Ericales o Ericaceae oMarcgraviaceae • Euasterids 1 Boraginales (Boraginaceae) Icacinales (Icacinaceae) Gentianales o Apocynaceae o Loganiaceae o Rubiaceae Lamiales o Acanthaceae o Gesneriaceae o Bignoniaceae o Lamiaceae o Plantaginaceae o Verbenaceae Solanales oConvolvulaceae o Solanaceae • Euasterids 2 o Asteraceae Lamiales Acanthaceae 2.600 spp, 250 gêneros ervas, arbustos, lianas distribuição pantropical 98 spp de trepadeiras no Neotrópico Mendoncia 75 spp Justicia 490 spp/13 escandentes Ruellia 230 spp/4 escandentes Introduzidas: (invasoras) Asystasia 1 sp Thunbergia 4 spp Asystasia gangetica http://botany.si.edu/lianas/docs/ACANTHACEAE.pdf • flores bissexuais • sépalas 4-5, conatas, desiguais • corola tubular, 5-lobadas • estames 4, iguais ou não • ovário súpero, bilocular • frutos diversos, geralmente cápsulas, com gancho placentário Acanthaceae Thunbergia alata Thunbergia - gênero com 4 spp nao nativas ao Neotrópico. Thunbergia fragrans Mendoncia cordata - liana volúvel, com frutos carnosos. Ruellia inflata Justicia brasiliensis Anisacanthus ramosissimus Thunbergia grandiflora - caules com floema interxilemático (formando faixas que se assemelham a raios largos) Mendoncia - caules com xilema disperso Justicia Cistolitos Thunbergia grandiflora - espécie invasora no Neotrópico Lamiales Gesneriaceae 150 gêneros; 3000 spp pantropical 56 gêneros e 1800 spp neotropicais Trepadeiras 14 gêneros e 112 spp -
Thunbergia Grandiflora1
Fact Sheet FPS-580 October, 1999 Thunbergia grandiflora1 Edward F. Gilman2 Introduction From early summer until late winter this vigorously twining vine bears hanging clusters of large, lavender-blue flowers that are 3 inches in diameter (Fig. 1). These flowers are bell-shaped and have a white throat. The broad, heart-shaped leaves of the Sky Flower are soft and dark green. The fruits are inconspicuous seed capsules. General Information Scientific name: Thunbergia grandiflora Pronunciation: thun-BER-jee-uh gran-diff-FLOR-ruh Common name(s): Bengal Clock Vine, Sky Vine Family: Acanthaceae Plant type: vine USDA hardiness zones: 9B through 11 (Fig. 2) Planting month for zone 8: year round Planting month for zone 9: year round Planting month for zone 10 and 11: year round Origin: not native to North America Uses: cascading down a wall; container or above-ground Figure 1. Bengal Clock Vine. planter Availablity: grown in small quantities by a small number of Growth rate: fast nurseries Texture: medium Description Foliage Height: depends upon supporting structure Spread: depends upon supporting structure Leaf arrangement: opposite/subopposite Plant habit: spreading Leaf type: simple Plant density: moderate Leaf margin: undulate 1.This document is Fact Sheet FPS-580, one of a series of the Environmental Horticulture Department, Florida Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida. Publication date: October, 1999 Please visit the EDIS Web site at http://edis.ifas.ufl.edu. 2. Edward F. Gilman, professor, Environmental Horticulture Department, Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, 32611. -
The Whole and the Parts: Relationships Between Floral Architecture and Floral Organ Shape, and Their Repercussions on the Interpretation of Fragmentary Floral Fossils
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2008 The whole and the parts: relationships between floral architecture and floral organ shape, and their repercussions on the interpretation of fragmentary floral fossils Endress, P K Abstract: Floral architecture and floral organ shape are interrelated to some extent as can be seen inthe diversity of extant angiosperm groups. The shape of fragmentary fossil material, such as single organs, may therefore give hints for the reconstruction of the architecture of a flower. This study is partly a review and partly provides original material and new points of view on organ-architecture interrelationships. Several topics are illustrated with examples: (1) autonomous and imprinted shape, exemplified by cuneate organs, especially stamens; (2) conditions for valvate anther dehiscence; (3) lability in number and shape of reduced organs that have decreased in size and lost their original function; (4) long hairs as filling material of irregular spaces; (5) architectural conditions for the presence of orthotropous ovules; (6) structural differences between exposed and covered organ parts in bud; and (7) sepal aestivation and petal elaboration. DOI: https://doi.org/10.3417/2006190 Posted at the Zurich Open Repository and Archive, University of Zurich ZORA URL: https://doi.org/10.5167/uzh-11688 Journal Article Published Version Originally published at: Endress, P K (2008). The whole and the parts: relationships between floral architecture and floral organ shape, and their repercussions on the interpretation of fragmentary floral fossils. Annals of the Missouri Botanical Garden, 95(1):101-120. -
Thunbergia Alata Black-Eye Susan Vine Acanthaceae
Thunbergia alata Black-eye Susan vine Acanthaceae Forest Starr, Kim Starr, and Lloyd Loope United States Geological Survey--Biological Resources Division Haleakala Field Station, Maui, Hawai'i April, 2003 OVERVIEW T. alata (black-eye Susan vine), native to tropical eastern Africa, is a sprawling vine that is often cultivated for its attractive flowers. It is widely cultivated and naturalized in other tropical regions of the world. In Hawai'i, T. alata was first reported from O'ahu in 1864-1865 and is now known from at least Kaua'i, Moloka'i, East Maui, and in Hilo and Volcano Village, Hawai'i (Wagner et al. 1999). On Maui, this plant is also popular in the landscape and is cultivated and naturalized from Ha'iku to Keokea, at approximately 300- 4,000 ft (91-1,219 m) elevation, in relatively moist and dry sites. It is probably too widespread for island wide control. It could be controlled if found in natural areas. TAXONOMY Family: Acanthaceae (Acanthus family) (Wagner et al. 1999). Latin name: Thunbergia alata Bojer (Wagner et al. 1999). Synonyms: None known. Common names: Black-eye Susan vine (Wagner et al. 1999). Taxonomic notes: The genus Thunbergia is made up of about 200 species from warm areas of central and southern Africa, Madagascar, and Asia (Wagner et al. 1999). Nomenclature: The genus is named after the Swedish botanist and explorer, Carl Peter Thunberg (1743-1822) (Turner and Wasson 1997). Related species in Hawai'i: Several cultivars of T. alata exist including "Alba" with white flowers and dark purple-brown centers, "Bakeri" with snow-white flowers and white centers, and "Suzie hybrids" with orange-yellow or white flowers with dark centers (Brickell and Zuk 1997).