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This Thesis Has Been Submitted in Fulfilment of the Requirements for a Postgraduate Degree (E.G
This thesis has been submitted in fulfilment of the requirements for a postgraduate degree (e.g. PhD, MPhil, DClinPsychol) at the University of Edinburgh. Please note the following terms and conditions of use: This work is protected by copyright and other intellectual property rights, which are retained by the thesis author, unless otherwise stated. A copy can be downloaded for personal non-commercial research or study, without prior permission or charge. This thesis cannot be reproduced or quoted extensively from without first obtaining permission in writing from the author. The content must not be changed in any way or sold commercially in any format or medium without the formal permission of the author. When referring to this work, full bibliographic details including the author, title, awarding institution and date of the thesis must be given. Molecular Species Delimitation, Taxonomy and Biogeography of Sri Lankan Gesneriaceae Subhani Wathsala Ranasinghe Doctor of Philosophy The University of Edinburgh Royal Botanic Garden Edinburgh 2017 Declaration I hereby declare that the work contained in this thesis is my own unless otherwise acknowledged and cited. This thesis has not in whole or in part been previously presented for any degree Subhani Wathsala Ranasinghe 24th January 2017. i Abstract The plant family Gesneriaceae is represented in Sri Lanka by six genera: Aeschynanthus, Epithema, Championia, Henckelia, Rhynchoglossum and Rhynchotechum, with 13 species (plus one subspecies/variety) of which ten are endemic including the monotypic genus Championia, according to the last revision in 1981. They are exclusively distributed in undisturbed habitats, and some have high ornamental value. The species are morphologically diverse, but face a problem of taxonomic delineation, which is further complicated by the presence of putative hybrids. -
Progress on Southeast Asia's Flora Projects
Gardens' Bulletin Singapore 71 (2): 267–319. 2019 267 doi: 10.26492/gbs71(2).2019-02 Progress on Southeast Asia’s Flora projects D.J. Middleton1, K. Armstrong2, Y. Baba3, H. Balslev4, K. Chayamarit5, R.C.K. Chung6, B.J. Conn7, E.S. Fernando8, K. Fujikawa9, R. Kiew6, H.T. Luu10, Mu Mu Aung11, M.F. Newman12, S. Tagane13, N. Tanaka14, D.C. Thomas1, T.B. Tran15, T.M.A. Utteridge16, P.C. van Welzen17, D. Widyatmoko18, T. Yahara14 & K.M. Wong1 1Singapore Botanic Gardens, National Parks Board, 1 Cluny Road, 259569 Singapore [email protected] 2New York Botanical Garden, 2900 Southern Boulevard, Bronx, New York, 10458, USA 3Auckland War Memorial Museum Tāmaki Paenga Hira, Private Bag 92018, Auckland 1142, New Zealand 4Ecoinformatics and Biodiversity, Department of Bioscience, Aarhus University Building 1540, Ny Munkegade 114, Aarhus C DK 8000, Denmark 5The Forest Herbarium, National Park, Wildlife and Plant Conservation Department, 61 Phahonyothin Rd., Chatuchak, Bangkok 10900, Thailand 6Herbarium, Forest Research Institute Malaysia, Kepong, Selangor 52109, Malaysia 7School of Life and Environmental Sciences, University of Sydney, NSW 2006, Australia 8Department of Forest Biological Sciences, College of Forestry & Natural Resources, University of the Philippines - Los Baños, College, 4031 Laguna, Philippines 9Kochi Prefectural Makino Botanical Garden, 4200-6 Godaisan, Kochi, 7818125, Japan 10Southern Institute of Ecology, Vietnam Academy of Science and Technology, 01 Mac Dinh Chi Street, District 1, Ho Chi Minh City, Vietnam 11Forest -
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 -
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. -
A New Definition of the Genus Petrocodon (Gesneriaceae)
Phytotaxa 23: 49–67 (2011) ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ Article PHYTOTAXA Copyright © 2011 Magnolia Press ISSN 1179-3163 (online edition) A new definition of the genus Petrocodon (Gesneriaceae) ANTON WEBER1,4, YI-GANG WEI2, CARMEN PUGLISI3, FANG WEN2, VERONIKA MAYER1 & MICHAEL MÖLLER3,4 1 Department of Structural and Functional Botany, Faculty of Biodiversity, University of Vienna, Austria 2 Guangxi Institute of Botany, Guangxi Zhuang Autonomous Region and the Chinese Academy of Sciences, Guilin 541006, China 3 Royal Botanic Garden Edinburgh, 20A Inverleith Row, Edinburgh EH3 5LR, Scotland, U.K. 4 Authors for correspondence; e-mails: [email protected], [email protected] Abstract Based on molecular studies, the small Chinese genus Petrocodon (two species and one variety) has been recently enlarged to include the monotypic genera Calcareoboea, Paralagarosolen and Tengia. It is shown here that the (6–7) species of Lagarosolen, the monotypic Dolicholoma, a few species of Didymocarpus, and a number of new species that have recently been published (but not formally described) under Petrocodon and Lagarosolen should be included in this genus. This raises the size of the genus from five to around 20 species. With respect to the floral diversity (corolla form, size, and coloration; with the exception of Tengia, the androecium is always diandrous) and inferred pollination syndromes (different forms of melittophily, ornithophily, psycho- and/or sphingophily), Petrocodon represents one of the most varied genera of Old World Gesneriaceae, comparable to some New World genera. Key words: Calcareoboea, Didymocarpus, Dolicholoma, Lamiales, Lagarosolen, molecular systematics, Paralagarosolen, pollination syndromes, Tengia Introduction A recent molecular phylogenetic study (Möller et al. -
The First Glimpse of Streptocarpus Ionanthus (Gesneriaceae) Phylogenomics: Analysis of Five Subspecies’ Chloroplast Genomes
plants Article The First Glimpse of Streptocarpus ionanthus (Gesneriaceae) Phylogenomics: Analysis of Five Subspecies’ Chloroplast Genomes Cornelius M. Kyalo 1,2,3 , Zhi-Zhong Li 2, Elijah M. Mkala 1,2,3 , Itambo Malombe 4, Guang-Wan Hu 1,3,* and Qing-Feng Wang 1,3 1 Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, Chinese Academy of Sciences, Wuhan 430074, China; [email protected] (C.M.K.); [email protected] (E.M.M.); [email protected] (Q.-F.W.) 2 University of Chinese Academy of Sciences, Beijing 100049, China; [email protected] 3 Sino-Africa Joint Research Center, Chinese Academy of Sciences, Wuhan 430074, China 4 East African Herbarium, National Museums of Kenya, P.O. Box 45166-00100 Nairobi, Kenya; [email protected] * Correspondence: [email protected] Received: 2 March 2020; Accepted: 2 April 2020; Published: 4 April 2020 Abstract: Streptocarpus ionanthus (Gesneriaceae) comprise nine herbaceous subspecies, endemic to Kenya and Tanzania. The evolution of Str. ionanthus is perceived as complex due to morphological heterogeneity and unresolved phylogenetic relationships. Our study seeks to understand the molecular variation within Str. ionanthus using a phylogenomic approach. We sequence the chloroplast genomes of five subspecies of Str. ionanthus, compare their structural features and identify divergent regions. The five genomes are identical, with a conserved structure, a narrow size range (170 base pairs (bp)) and 115 unique genes (80 protein-coding, 31 tRNAs and 4 rRNAs). Genome alignment exhibits high synteny while the number of Simple Sequence Repeats (SSRs) are observed to be low (varying from 37 to 41), indicating high similarity. -
A Publication Devoted to Tropical Plants, with Emphasis On
THE STATE OF MOLECULAR STUDIES IN THE FAMILY GESNERIACEAE: AREVIEW MICHAEL MO¨ LLER* Royal Botanic Garden Edinburgh, 20A Inverleith Row, Edinburgh EH5 3LR, Scotland, UK. Email: [email protected] JOHN L. CLARK The University of Alabama, Dept. of Biological Sciences, Box 870345, Tuscaloosa, AL 35487-0345, USA. A Publication Devoted to Tropical Plants, with Emphasis on Epiphytic Plant Families Selbyana 31(2): 95–125. 2013. THE STATE OF MOLECULAR STUDIES IN THE FAMILY GESNERIACEAE: AREVIEW MICHAEL MO¨ LLER* Royal Botanic Garden Edinburgh, 20A Inverleith Row, Edinburgh EH5 3LR, Scotland, UK. Email: [email protected] JOHN L. CLARK The University of Alabama, Dept. of Biological Sciences, Box 870345, Tuscaloosa, AL 35487-0345, USA. ABSTRACT. Sparked by the publication of large phylogenetic studies and major generic redefinitions in the Gesneriaceae, we review this growing body of molecular studies on the family. Different aspects of molecular data and their use in Gesneriaceae systematics are considered including conceptual challenges on the phylogenetic work undertaken to date as well as an overview of taxon sampling in the family. Molecular data are currently available for 70 of 72 recognized New World genera and 64 of 68 Old World genera. Many of the smaller genera and some of the larger genera are completely sampled. Current knowledge of tribal and generic delineations and relationships among the New World genera is relatively advanced. In contrast, intergeneric relationships and tribal arrangements are mostly unresolved for the Old World genera. In this paper we illustrate and summarize the published phylogenetic work in composite phylogenies with an emphasis on the most pertinent and accurate molecular systematic studies. -
Sinningia Speciosa 57 Seed Fund – Hybrids ‘Lorna Ohlgren’ Gussie Farrice Dave Zaitlin 61 Information About the Gesneriad 31 Gesneriads Index 2017 Society, Inc
GesThe Journal forn Gesneriade Growersria ds Volume 68 ~ Number 2 Second Quarter 2018 Return to Table of Contents RETURN TO TABLE OF CONTENTS The Journal for Gesneriad Growers Volume 68 ~ Number 2 Gesneriads Second Quarter 2018 41 Experiences Growing the Gesneriads FEATURES from Southern Chile 5 The 2017 Lawrenceville School in Cuba Program: Trekking from Guantánamo Bob Stewart to the North Coast through the 44 Christopheria xantha Alejandro de Humboldt National Park Dale Martens John L. Clark 46 Rarely Seen, Rarely Done: Merging 11 Delivering the Power of the Sun Two Passions to Cuba’s Alejandro de Humboldt Drew Norris National Park Annika Goldman DEPARTMENTS 13 From the Garden State to the Pearl 3 Message from the President of the Antilles 4 From The Editor Grace Cangiano 35 Botanical Review No. 46 16 From Guantanamera to Polymita: A Cultural and Biological Expedition Bob Stewart to Cuba 40 Changes to Species Seed List 1Q18 50 Coming Events Hiroki Nagao 19 Cultivating Gesneriads in Greece Ray Coyle and Karyn Cichocki 51 Gesneriad Registrations Panagiotis Mperetzikis 22 There’s Something for Everyone in Irina Nicholson New England! 52 Donations Gloria Utzig and Maureen Pratt Betsy Gottshall 26 Gesneriad Hybridizers Association 54 Back to Basics: Convention Fun! Meeting Dale Martens 27 Introducing Sinningia speciosa 57 Seed Fund – Hybrids ‘Lorna Ohlgren’ Gussie Farrice Dave Zaitlin 61 Information about The Gesneriad 31 Gesneriads Index 2017 Society, Inc. Cover Back Cover Gesneria bracteosa Primulina ‘Silver Feather’ Photo: John L. Clark -
Expression Pattern of Cyclike Genes Relating to a Dorsalized
Journal of Systematics and Evolution 48 (5): 309–317 (2010) doi: 10.1111/j.1759-6831.2010.00091.x Expression pattern of CYC-like genes relating to a dorsalized actinomorphic flower in Tengia (Gesneriaceae) 1Hong-Bo PANG 2Qing-Wen SUN 2Shun-Zhi HE 1Yin-Zheng WANG∗ 1(State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China) 2(Guiyang College of Traditional Chinese Medicine, Guiyang 550002, China) Abstract Tengia has been called a “natural peloria” in the family Gesneriaceae because it exhibits an almost perfect actinomorphic flower from whorl one to whorl three. It would be especially interesting to know whether or how CYC-like gene activities are related to this type of perfect actinomorphic flower. To address this, we have isolated four CYC-like TCP genes and carried out an investigation on their expression patterns in Tengia. TsCYC1C and TsCYC1D have similar expression patterns with strong signals being detected in all five petals and stamens, whereas TsCYC2A and TsCYC2B are only transiently expressed in the very early floral meristem. Our results suggest that the expansion of the expressions of TsCYC1C and TsCYC1D from the dorsal to the ventral petals is likely responsible for the evolutionary formation of the fully dorsalized actinomorphic corolla, that is, an expanded functional domain of CYC-like gene dorsal identity in Tengia corolla. However, the expressions of TsCYC1C and TsCYC1D are not correlated with stamen abortion; therefore, TsCYC genes do not functionally repress the stamen development in Tengia flowers. This is probably due to changed cis-activities that result in the cell cycle-related genes uncoupling from the TsCYC regulatory pathway in Tengia. -
The Leipzig Catalogue of Plants (LCVP) ‐ an Improved Taxonomic Reference List for All Known Vascular Plants
Freiberg et al: The Leipzig Catalogue of Plants (LCVP) ‐ An improved taxonomic reference list for all known vascular plants Supplementary file 3: Literature used to compile LCVP ordered by plant families 1 Acanthaceae AROLLA, RAJENDER GOUD; CHERUKUPALLI, NEERAJA; KHAREEDU, VENKATESWARA RAO; VUDEM, DASHAVANTHA REDDY (2015): DNA barcoding and haplotyping in different Species of Andrographis. In: Biochemical Systematics and Ecology 62, p. 91–97. DOI: 10.1016/j.bse.2015.08.001. BORG, AGNETA JULIA; MCDADE, LUCINDA A.; SCHÖNENBERGER, JÜRGEN (2008): Molecular Phylogenetics and morphological Evolution of Thunbergioideae (Acanthaceae). In: Taxon 57 (3), p. 811–822. DOI: 10.1002/tax.573012. CARINE, MARK A.; SCOTLAND, ROBERT W. (2002): Classification of Strobilanthinae (Acanthaceae): Trying to Classify the Unclassifiable? In: Taxon 51 (2), p. 259–279. DOI: 10.2307/1554926. CÔRTES, ANA LUIZA A.; DANIEL, THOMAS F.; RAPINI, ALESSANDRO (2016): Taxonomic Revision of the Genus Schaueria (Acanthaceae). In: Plant Systematics and Evolution 302 (7), p. 819–851. DOI: 10.1007/s00606-016-1301-y. CÔRTES, ANA LUIZA A.; RAPINI, ALESSANDRO; DANIEL, THOMAS F. (2015): The Tetramerium Lineage (Acanthaceae: Justicieae) does not support the Pleistocene Arc Hypothesis for South American seasonally dry Forests. In: American Journal of Botany 102 (6), p. 992–1007. DOI: 10.3732/ajb.1400558. DANIEL, THOMAS F.; MCDADE, LUCINDA A. (2014): Nelsonioideae (Lamiales: Acanthaceae): Revision of Genera and Catalog of Species. In: Aliso 32 (1), p. 1–45. DOI: 10.5642/aliso.20143201.02. EZCURRA, CECILIA (2002): El Género Justicia (Acanthaceae) en Sudamérica Austral. In: Annals of the Missouri Botanical Garden 89, p. 225–280. FISHER, AMANDA E.; MCDADE, LUCINDA A.; KIEL, CARRIE A.; KHOSHRAVESH, ROXANNE; JOHNSON, MELISSA A.; STATA, MATT ET AL. -
(Gesneriaceae), As Inferred by Phylogenetic and Morphological Data
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/302366154 Generic recircumscription in the Loxocarpinae (Gesneriaceae), as inferred by phylogenetic and morphological data Article in Taxon · May 2016 Impact Factor: 3.3 · DOI: 10.12705/652.5 READS 57 5 authors, including: Tze Leong Yao Richard Ian Milne Forest Research Institute Malaysia (FRIM) The University of Edinburgh 19 PUBLICATIONS 54 CITATIONS 61 PUBLICATIONS 1,970 CITATIONS SEE PROFILE SEE PROFILE Michael Moeller David John Middleton Royal Botanic Garden Edinburgh Singapore Botanic Gardens 165 PUBLICATIONS 2,028 CITATIONS 134 PUBLICATIONS 525 CITATIONS SEE PROFILE SEE PROFILE Available from: Tze Leong Yao Retrieved on: 17 May 2016 TAXON 65 (2) • April 2016: 277–292 Puglisi & al. • Phylogeny of Loxocarpinae Generic recircumscription in the Loxocarpinae (Gesneriaceae), as inferred by phylogenetic and morphological data Carmen Puglisi,1 Tze Leong Yao,2 Richard Milne,3 Michael Möller1 & David J. Middleton4 1 Royal Botanic Garden Edinburgh, 20A Inverleith Row, Edinburgh EH3 5LR, U.K. 2 Forest Research Institute Malaysia, 52109 Kepong, Selangor, Malaysia 3 University of Edinburgh, Institute of Molecular Plant Sciences, Edinburgh EH9 3JH, U.K. 4 Herbarium, Singapore Botanic Gardens, National Parks Board, 1 Cluny Road, Singapore 259569 Author for correspondence: Carmen Puglisi, [email protected] ORCID MM, http://orcid.org/0000-0002-2819-0323 DOI http://dx.doi.org/10.12705/652.5 Abstract The Loxocarpinae, also known as the “Boea group”, are the subtribe of Gesneriaceae which includes Boea and a number of segregated genera and close relatives. This group currently comprises over 200 species in 15 genera. -
The Systematic Distribution of Vascular Epiphytes: an Update
Selbyana 9: 2-22 THE SYSTEMATIC DISTRIBUTION OF VASCULAR EPIPHYTES: AN UPDATE w. JOHN KREss Marie Selby Botanical Gardens, 811 South Palm Avenue, Sarasota, Florida 33577 ABSTRACT. The list of vascular plant families and genera containing epiphytic species published by Madison (1977) is updated here. Ten percent (23,456 species) of all vascular plant species are epiphytes. Seven percent (876) of the genera, 19 percent (84) of the families, 45 percent (44) of the orders and 75 percent (6) of the classes contain epiphytes. Twenty-three families contain over 50 epiphytic species each. The Orchidaceae is the largest family of epiphytes, containing 440 epiphytic genera and 13,951 epiphytic species. Forty-three genera of vascular plants each contain over 100 epiphytic species. In 1977 Madison published a list of the vas those plants that normally spend their entire life cular plant families and genera that contain epi cycle perched on another plant and receive all phytic species. Madison compiled this list from mineral nutrients from non-terrestrial sources. literature reports, consultation with taxonomic Hemi~epiphytes normally spend only part oftheir specialists, and a survey of herbarium material. life cycle perched on another plant and thus some He reported that 65 families contain 850 genera mineral nutrients are received from terrestrial and 28,200 species of epiphytes. His total ac sources. Hemi-epiphytes either begin their life counted for about ten percent of all species of cycle as epiphytes and eventually send roots and vascular plants. shoots to the ground (primary hemi-epiphytes), Madison's list was the most comprehensive or begin as terrestrially established seedlings that compilation of vascular epiphytes since the works secondarily become epiphytic by severing all of Schimper (1888) and Richards (1952) upon connections with the ground (secondary hemi which it was partly based.