The Family Gesneriaceae As Example for the Biological Extinction in Western Ecuador
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Keene, Jeremy 11-21-13
A Reassessment of Monopyle (Gloxinieae:Gesneriaceae) A dissertation presented to the faculty of the College of Arts and Sciences of Ohio University In partial fulfillment of the requirements for the degree Doctor of Philosophy Jeremy L. Keene December 2013 © 2013 Jeremy L. Keene. All Rights Reserved. 2 This dissertation titled A Reassessment of Monopyle (Gloxinieae: Gesneriaceae) by JEREMY L. KEENE has been approved for the Department of Environmental and Plant Biology and the College of Arts and Sciences by Harvey E. Ballard, Jr. Associate Professor of Environmental and Plant Biology Robert Frank Dean, College of Arts and Sciences 3 ABSTRACT KEENE, JEREMY L., Ph.D., December 2013, Environmental and Plant Biology A Reassessment of Monopyle (Gloxinieae: Gesneriaceae) Director of Dissertation: Harvey E. Ballard, Jr. Monopyle Moritz ex Benth. is a genus of herbs or suffrutescent herbs distributed from Guatemala southward into northern South America. This assemblage of plants is characterized by the presence of anisophyllous leaves, uncinate trichomes, and campanulate flowers. The genus was last revised in 1945 by Conrad Morton. Since that time, few additional taxa have been recognized. It was comprised of 22 described species in 2011, with two infraspecific taxa. Also, there has been limited sampling of this genus for phylogenetic studies to assess the evolution of the genus. There were two primary foci of this research, a morphological characterization of the species within Monopyle and molecular analyses of the species within Monopyle and other closely related genera. A detailed morphological analysis was performed to determine the morphological differentiation between taxa. This analysis also confirmed which diagnostic characters identified in previous studies were valid and useful. -
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. -
Trends in Nectar Concentration and Hummingbird Visitation
SIT Graduate Institute/SIT Study Abroad SIT Digital Collections Independent Study Project (ISP) Collection SIT Study Abroad Fall 2016 Trends in Nectar Concentration and Hummingbird Visitation: Investigating different variables in three flowers of the Ecuadorian Cloud Forest: Guzmania jaramilloi, Gasteranthus quitensis, and Besleria solanoides Sophie Wolbert SIT Study Abroad Follow this and additional works at: https://digitalcollections.sit.edu/isp_collection Part of the Animal Studies Commons, Community-Based Research Commons, Environmental Studies Commons, Latin American Studies Commons, and the Plant Biology Commons Recommended Citation Wolbert, Sophie, "Trends in Nectar Concentration and Hummingbird Visitation: Investigating different variables in three flowers of the Ecuadorian Cloud Forest: Guzmania jaramilloi, Gasteranthus quitensis, and Besleria solanoides" (2016). Independent Study Project (ISP) Collection. 2470. https://digitalcollections.sit.edu/isp_collection/2470 This Unpublished Paper is brought to you for free and open access by the SIT Study Abroad at SIT Digital Collections. It has been accepted for inclusion in Independent Study Project (ISP) Collection by an authorized administrator of SIT Digital Collections. For more information, please contact [email protected]. Wolbert 1 Trends in Nectar Concentration and Hummingbird Visitation: Investigating different variables in three flowers of the Ecuadorian Cloud Forest: Guzmania jaramilloi, Gasteranthus quitensis, and Besleria solanoides Author: Wolbert, Sophie Academic -
Gesneriads First Quarter 2018
GesThe Journal forn Gesneriade Growersria ds Volume 68 ~ Number 1 First Quarter 2018 Return to Table of Contents RETURN TO TABLE OF CONTENTS The Journal for Gesneriad Growers Volume 68 ~ Number 1 Gesneriads First Quarter 2018 FEATURES DEPARTMENTS 5 Saintpaulia, the NEW Streptocarpus 3 Message from the President Winston Goretsky Julie Mavity-Hudson 9 Style Guide for Writers 4 From The Editor Jeanne Katzenstein Peter Shalit 10 Gesneriads at the Liuzhou Arts Center 18 Gesneriad Registrations Wallace Wells Irina Nicholson 24 Flower Show Awards 42 Changes to Hybrid Seed List 4Q17 Paul Susi Gussie Farrice 25 Gesneriads POP in New England! 46 Coming Events Maureen Pratt Ray Coyle and Karyn Cichocki 28 62nd Annual Convention of The 47 Flower Show Roundup Gesneriad Society 51 Back to Basics: Gesneriad Crafts 37 Convention Speakers Dale Martens Dee Stewart 55 Seed Fund – Species 39 Petrocosmeas in the United Kingdom Carolyn Ripps Razvan Chisu 61 Information about The Gesneriad 43 Gasteranthus herbaceus – A white- Society, Inc. flowered Gasteranthus from the northern Andes Dale Martens with John L. Clark Cover Eucodonia ‘Adele’ grown by Eileen McGrath Back Cover and exhibited at the New York State African Petrocosmea ‘Stone Amethyst’, hybridized, Violet Convention Show, October 2017. grown, and photographed by Andy Kuang. Photo: Bob Clark See New Registrations article, page 18. Editor Business Manager The Gesneriad Society, Inc. Peter Shalit Michael A. Riley The objects of The Gesneriad [email protected] [email protected] Society are to afford -
GESNERIACEAE ENDÉMICAS DEL PERÚ Versión Online ISSN 1727-9933 © Facultad De Ciencias Biológicas UNMSM
Rev. peru. biol. Número especial 13(2): 359s - 365s (Diciembre 2006) El libro rojo de las plantas endémicas del Perú. Ed.: Blanca León et al. GESNERIACEAE ENDÉMICAS DEL PERÚ Versión Online ISSN 1727-9933 © Facultad de Ciencias Biológicas UNMSM Gesneriaceae endémicas del Perú Irayda Salinas 1 y Blanca León 1,2 1 Museo de Historia Natural, Resumen Av. Arenales 1256, Aptdo. 14-0434, Lima 14, Perú. La familia Gesneriaceae es reconocida en el Perú por presentar 31 géneros y 141 espe- [email protected] cies (Brako & Zarucchi, 1993; Ulloa Ulloa et al., 2004), mayormente hierbas y arbustos. En 2 Plant Resources Center, este trabajo reconocemos como endemismos 36 especies y tres variedades en doce University of Texas at géneros. El género Besleria es el más rico en especies endémicas. Las Gesneriaceae Austin, Austin TX 78712 endémicas ocupan las regiones Bosques Húmedos Amazónicos y de Bosques Muy EE.UU. Húmedos Montanos, entre los 100 y 2900 m de altitud. Ocho taxones endémicos de [email protected] Gesneriaceae se encuentran representados dentro del Sistema Nacional de Áreas Natu- rales Protegidas por el Estado. Palabras claves: Gesneriaceae, Besleria, Perú, endemismo, plantas endémicas. Abstract The Gesneriaceae are represented in Peru by 31 genera and 141 species (Brako & Zarucchi, 1993; Ulloa Ulloa et al., 2004), mainly herbs and shrubs. Here we recognize as endemics 36 species and three varieties in twelve genera. Besleria is the genus with the largest number of endemic species. Peru’s endemic Gesneriaceae are found in the Humid Lowland Amazonian Forest and Very Humid Montane Forest regions, between 100 and 2900 m elevation. -
Complete List of Gesneriad Species
Gesneriaceae Currently Aeschynanthus batakiorum Aeschynanthus jouyi Accepted Species Names Aeschynanthus batesii Aeschynanthus kermesinus Aeschynanthus brachyphyllus Aeschynanthus lancilimbus Updated 4/1/21 Aeschynanthus bracteatus Aeschynanthus lasianthus (originally SI Checklist 6-15-12 Aeschynanthus breviflorus Aeschynanthus lasiocalyx previously updated to 6/1/16) Aeschynanthus burttii Aeschynanthus lepidospermus https://padme.rbge.org.uk/grc Aeschynanthus buxifolius Aeschynanthus leptocladus Aeschynanthus calanthus Aeschynanthus leucothamnos Gesnereaceae Resource Centre - Aeschynanthus cambodiensis # Aeschynanthus ligustrinus create a checklist (rbge.org. -
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 -
Network Scan Data
Selbyana 5(1):61-93.1978. MISCELLANEOUS TRANSFERS AND NEW SPECIES OF NEOTROPICAL GESNERIACEAE Hans Wiehler* A study of plant material recently brought into cultivation, biosystema tic work on generic relationships, and herbarium and literature research on the typification of neotropical Gesneriaceae necessitate the generic transfer of the following species, in alphabetical order: 1. Codonanthopsis dissimulata (H. E. Moore) Wiehler, comb. nov. Codonanthe dissimulata H. E. Moore, Baileya 19(1):25. 1973. TYPE: M. H. Stone 1143 (HOLOTYPE: BH). TYPE LOCALITY: Peru: Iquitos. DISTRIBUTION: Peru: Loreto, Huanuco; Brazil: Acre, Amazonas; Venezuela: Amazonas, Delta Amacuro; Guyana. In a synopsis of Codonanthe (Mart.) Hanst., Moore (1973a) proposed a union of the small genus Codonanthopsis Mansf. with Codonanthe, and described a new species, Codonanthe dissimulata, from material in cultiva tion at Cornell University. A study of generic relationships in the neotropical Gesneriaceae (Wiehler, 1979) reveals, however, that the differences between these two taxa are on the generic and not on the sectional level. Codonanthe and Codonanthopsis differ consistently: 1) in plant habit: the stiff and as cending branches of the species of Codonanthopsis have large (ca. 10-15 X 4-6 cm) and fleshy, strongly anisophyllolls leaves, of which the smaller of the pair is typically stipule-like and early caducous, while the species of Codo nanthe are vine-like, with small, equal or subequalleaves; 2) the base chro mosome number in Codonanthopsis is x = 9, but in Codonanthe x = 8; 3) the connective of the anther cells is narrow in all species of Codonanthopsis, as in the rest of the Gesnerioideae, but the trade mark of Codonanthe is a pecu liar broad connective, spatially separating the two thecae. -
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. -
Ecology of Plant Hummingbird Interactions in Maquipucuna, Ecuador
ECOLOGY OF PLANT HUMMINGBIRD INTERACTIONS IN MAQUIPUCUNA, ECUADOR Tatiana Santander, Esteban Guevara, Francisco Tobar, Holger Beck, Nicole Büttner, Andrea Nieto, Andrés Marcayata, Friederike Richter, María José Gavilanes, Cristian Poveda, Bryan Rojas, Rafael Wüest, Carolina Bello and Catherine H. Graham October 22, 2020 Contents 1. Introduction and project overview 1 2. Methodological Approach 2 Field transects ................................ 2 Timelapse cameras .............................. 5 3. Resulting patterns 5 Planthummingbird interactions ........................ 5 Plants information and phenology ....................... 9 The Network of Interactions .......................... 12 4. Conclusions: 19 Acknowledgements 20 1. Introduction and project overview One of the main hypotheses for how so many related species can cooccur is resource partitioning where species use different resources, which limits competition among species and allows them to coexist. In the case of hummingbirds and plants, each hummingbird species forages on a distinct set of flowers and each flowering plant species is visited by a subset of hummingbirds. Interactions between plants and hummingbirds are mutually beneficial. These mutualistic hummingbirdplant interactions are important from a hummingbird perspective because hummingbirds require nectar to fuel their highenergy lifestyles where they often hover – an energetically costly behavior – to take nectar. From a plant perspective most hummingbirds pollinate flowers as they forage on nectar, though some hummingbirds take nectar from the base of the flower, cheating the flower from this service of pollination. The intricate web of interactions between hummingbirds and their food plants evolved over millennia as a result of diffuse coevolution which yielded a remarkable array of morphological forms and functions. Ongoing human activities, such as deforestation and climate change threaten these interaction webs, yet little is known as to how hummingbirds and their food plants will respond. -
A Phylogenetic Analysis of Tribes Beslerieae and Napeantheae (Gesneriaceae) and Evolution of Fruit Types: Parsimony and Maximum Likelihood Analyses of Ndhf Sequences
Systematic Botany (2000), 25(1): pp. 72±81 q Copyright 2000 by the American Society of Plant Taxonomists A Phylogenetic Analysis of Tribes Beslerieae and Napeantheae (Gesneriaceae) and Evolution of Fruit Types: Parsimony and Maximum Likelihood Analyses of ndhF Sequences JAMES F. S MITH Department of Biology, Boise State University, 1910 University Drive, Boise, Idaho 83725 Communicating Editor: James Manhart ABSTRACT. A cladistic analysis of tribes Beslerieae and Napeantheae revealed that both are monophyletic groups and that Napeantheae is sister to Beslerieae. These relationships are supported by parsimony and most models of maximum likelihood analysis, although with the F81 model, maximum likelihood places Napeantheae within Beslerieae making the latter tribe paraphyletic. All analyses indicate that within Besler- ieae, Besleria and Gasteranthus are sister genera. In parsimony analysis these two genera are sister to the remainder of the tribe whereas in the maximum likelihood analyses, Cremosperma is sister to Besleria/Gaster- anthus. Regardless of the analysis, there is a close relationship between clades comprised of dehiscent ¯eshy- fruited genera and those with indehiscent ¯eshy fruits. This is similar to Episcieae, implying that the tran- sition from dry capsular fruits to berries may require a two-step process where a ¯eshy dehiscent capsule is the ®rst stage followed by an indehiscent ¯eshy berry. The origin of stomata in islands, a characteristic common among Beslerieae and Napeantheae is discussed. Gesneriaceae comprise approximately 2,500± and subtending bracts on the in¯orescence, 2) one 3,700 species in 120±147 genera, distributed pri- trace, unilacunar nodal anatomy, 3) a petiole with marily in the tropics with a few temperate species a deep vascular crescent in cross section, 4) seeds in Europe, China, and Japan (Heywood 1978; Burtt without ¯eshy funiculi, and 5) an annular or semi- and Wiehler 1995). -
A Synoptical Classification of the Lamiales
Lamiales – Synoptical classification vers. 2.0 (in prog.) Updated: 13 December, 2005 A Synoptical Classification of the Lamiales Version 2.0 (in progress) Compiled by Richard Olmstead With the help of: D. Albach, B. Bremer, P. Cantino, C. dePamphilis, P. Garnock-Jones, R. Harley, L. McDade, E. Norman, B. Oxelman, J. Reveal, R. Scotland, J. Smith, E. Wallander, A. Weber, A. Wolfe, N. Young, M. Zjhra, and others [estimated # species in Lamiales = 22,000] 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. Lamiales – Synoptical classification vers. 2.0 (in prog.) Updated: 13 December, 2005 Acanthaceae (~201/3510) Durande, Notions Elém. Bot.: 265. 1782, nom. cons. – Synopsis compiled by R. Scotland & K. Vollesen (Kew Bull. 55: 513-589. 2000); probably should include Avicenniaceae. Nelsonioideae (7/ ) Lindl. ex Pfeiff., Nomencl.