Corybas Sulcatus (Grooved Helmet-Orchid)
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ITEX Discoveries
Plant Response to Climate Change: Integration of ITEX Discoveries Proceedings from the 9th ITEX Meeting AEL REPORT 1 ARCTIC ECOLOGY LABORATORY DEPARTMENT OF BOTANY & PLANT PATHOLOGY MICHIGAN STATE UNIVERSITY EAST LANSING, MI 48824 Plant Response to Climate Change: Integration of ITEX Discoveries Proceedings from the 9th ITEX Meeting Compiled and edited by Robert D. Hollister Suggested Citation: Hollister, R.D. (editor). 1999. Plant Response to Climate Change: Integration of ITEX Discoveries. Proceedings from the 9th ITEX Meeting January 5-9, 1999. Arctic Ecology Laboratory Report 1, Michigan State University. East Lansing, MI. 117 p. This Report is available from: The Arctic Ecology Laboratory Department of Botany & Plant Pathology Michigan State University East Lansing, MI 48824 Telephone: 517 432-2399 i Foreword This compilation from the 1999 meeting of the International Tundra Experiment (ITEX) held at Michigan State University (MSU) demonstrates the considerable progress made since the 1990 founding meeting of ITEX which was also held at MSU. In the intervening nine years ITEX has become an established and well-known project. It has been used as a model for related endeavors. This document is intended to serve as an update on ITEX activities and an encouragement for continued integration and cooperation in the study of tundra plant response, and the linked feedback of this response, to climate change. The ITEX Steering Committee and I wish to thank Bob Hollister for his unflagging efforts as Conference Coordinator and compiler and editor of this report. The meeting was made possible with funding from the United States National Science Foundation Office of Polar Programs (grant number OPP 9714103). -
Seidenfaden Malaysia: 0.65 These Figures Are Surprisingly High, They Apply to Single Only. T
BIOGEOGRAPHY OF MALESIAN ORCHIDACEAE 273 VIII. Biogeographyof Malesian Orchidaceae A. Schuiteman Rijksherbarium/Hortus Botanicus, P.O. Box 9514, 2300 RA Leiden, The Netherlands INTRODUCTION The Orchidaceae outnumber far other in Malesia. At how- by any plant family present, accurate estimate of the of Malesian orchid is difficult to make. ever, an number species Subtracting the numberofestablishedsynonyms from the numberof names attributed to Malesian orchid species results in the staggering figure of 6414 species, with a retention of 0.74. This is ratio (ratio of ‘accepted’ species to heterotypic names) undoubtedly a overestimate, of the 209 Malesian orchid have been revised gross as most genera never their entire from availablerevisions estimate realis- over range. Extrapolating to a more tic retention ratio is problematic due to the small number of modern revisions and the different of treated. If look for Malesian of nature the groups we comparison at species wide ofretention ratios: some recently revised groups, we encounter a range Bulbophylluw sect. Uncifera (Vermeulen, 1993): 0.24 Dendrobium sect. Oxyglossum (Reeve & Woods, 1989): 0.24 Mediocalcar (Schuiteman, 1997): 0.29 Pholidota (De Vogel, 1988): 0.29 Bulbophyllum sect. Pelma (Vermeulen, 1993): 0.50 Paphiopedilum (Cribb, 1987, modified): 0.57 Dendrobium sect. Spatulata (Cribb, 1986, modified): 0.60. Correspondingly, we find a wide rangeof estimates for the ‘real’ numberof known Male- sian orchid species: from 2050 to 5125. Another approach would be to look at a single area, and to compute the retention ratio for the orchid flora of that area. If we do this for Java (mainly based on Comber, 1990), Peninsular Malaysia & Singapore (Seidenfaden & Wood, 1992) and Sumatra (J.J. -
Department of Sustainability, Environment, Water, Population and Communities; Formerly from Department of Primary Industries, Parks, Water and Environment (Tasmania)
The Minister included this species in the critically endangered category, effective from 26/02/2013. Advice to the Minister for Sustainability, Environment, Water, Population & Communities from the Threatened Species Scientific Committee (the Committee) on amendment to the list of Threatened Species under the Environment Protection and Biodiversity Conservation Act 1999 (EPBC Act) 1. Reason for Conservation Assessment by the Committee This advice follows assessment of information gathered through the Commonwealth’s partnership agreement with Tasmania, which is aimed at systematically reviewing species that are inconsistently listed under the EPBC Act and relevant Tasmanian legislation. The Committee provides the following assessment of the appropriateness of this species’ inclusion in the EPBC Act list of threatened species: Corybas sulcatus (grooved helmet-orchid) 2. Summary of Species Details Taxonomy Conventionally accepted as Corybas sulcatus (M.A.Clem. & D.L.Jones) G.N.Backh. Formerly Nematoceras sulcatum M.A.Clem. & D.L.Jones. State/Territory Listing This species is listed as endangered (as Nematoceras Status sulcatum) under the Tasmanian Threatened Species Protection Act 1995. Description A small, deciduous, tuberous terrestrial orchid that forms small clonal colonies. Leaves are solitary, circular (12–20 mm diameter) and flat to shallowly concave. They are light green above and silvery green beneath, with a thick-textured blade and fleshy leaf stalk 12–16 mm long. Flowers are 25–30 mm long and 10–14 mm wide, mostly dark red and held erect on a fleshy, green stalk that is 5–7 mm long (Clements and Jones, 2007). Distribution The grooved helmet-orchid is endemic to Macquarie Island (Tasmania). -
Lankesteriana IV
LANKESTERIANA 7(1-2): 229-239. 2007. DENSITY INDUCED RATES OF POLLINARIA REMOVAL AND DEPOSITION IN THE PURPLE ENAMEL-ORCHID, ELYTHRANTHERA BRUNONIS (ENDL.) A.S. GEORGE 1,10 2 3 RAYMOND L. TREMBLAY , RICHARD M. BATEMAN , ANDREW P. B ROWN , 4 5 6 7 MARC HACHADOURIAN , MICHAEL J. HUTCHINGS , SHELAGH KELL , HAROLD KOOPOWITZ , 8 9 CARLOS LEHNEBACH & DENNIS WIGHAM 1 Department of Biology, 100 Carr. 908, University of Puerto Rico – Humacao campus, Humacao, Puerto Rico, 00791-4300, USA 2 Natural History Museum, Cromwell Road, London SW7 5BD, UK 3 Department of Environment and Conservation, Species and Communities Branch, Locked Bag 104 Bentley Delivery Centre WA 6893, Australia 4 New York Botanic Garden, 112 Alpine Terrace, Hilldale, NJ 00642, USA 5 School of Life Sciences, University of Sussex, Falmer, Brighton, Sussex, BN1 9QG, UK 6 IUCN/SSC Orchid Specialist Group Secretariat, 36 Broad Street, Lyme Regis, Dorset, DT7 3QF, UK 7 University of California, Ecology and Evolutionary Biology, Irvine, CA 92697, USA 8 Massey University, Allan Wilson Center for Molecular Ecology and Evolution 9 Smithsonian Institution, Smithsonian Environmental Research Center, Box 28, Edgewater, MD 21037, USA 10 Author for correspondence: [email protected] RESUMEN. La distribución y densidad de los individuos dentro de las poblaciones de plantas pueden afectar el éxito reproductivo de sus integrantes. Luego de describir la filogenia de las orquideas del grupo de las Caladeniideas y su biología reproductiva, evaluamos el efecto de la densidad en el éxito reproductivo de la orquídea terrestre Elythranthera brunonis, endémica de Australia del Oeste. El éxito reproductivo de esta orquídea, medido como la deposición y remoción de polinios, fue evaluado. -
Orchid Historical Biogeography, Diversification, Antarctica and The
Journal of Biogeography (J. Biogeogr.) (2016) ORIGINAL Orchid historical biogeography, ARTICLE diversification, Antarctica and the paradox of orchid dispersal Thomas J. Givnish1*, Daniel Spalink1, Mercedes Ames1, Stephanie P. Lyon1, Steven J. Hunter1, Alejandro Zuluaga1,2, Alfonso Doucette1, Giovanny Giraldo Caro1, James McDaniel1, Mark A. Clements3, Mary T. K. Arroyo4, Lorena Endara5, Ricardo Kriebel1, Norris H. Williams5 and Kenneth M. Cameron1 1Department of Botany, University of ABSTRACT Wisconsin-Madison, Madison, WI 53706, Aim Orchidaceae is the most species-rich angiosperm family and has one of USA, 2Departamento de Biologıa, the broadest distributions. Until now, the lack of a well-resolved phylogeny has Universidad del Valle, Cali, Colombia, 3Centre for Australian National Biodiversity prevented analyses of orchid historical biogeography. In this study, we use such Research, Canberra, ACT 2601, Australia, a phylogeny to estimate the geographical spread of orchids, evaluate the impor- 4Institute of Ecology and Biodiversity, tance of different regions in their diversification and assess the role of long-dis- Facultad de Ciencias, Universidad de Chile, tance dispersal (LDD) in generating orchid diversity. 5 Santiago, Chile, Department of Biology, Location Global. University of Florida, Gainesville, FL 32611, USA Methods Analyses use a phylogeny including species representing all five orchid subfamilies and almost all tribes and subtribes, calibrated against 17 angiosperm fossils. We estimated historical biogeography and assessed the -
Orchid Seed Coat Morphometrics. Molvray and Kores. 1995
American Journal of Botany 82(11): 1443-1454. 1995 . CHARACTER ANALYSIS OF THE SEED COAT IN SPIRANTHOIDEAE AND ORCHIDOIDEAE, WITH SPECIAL REFERENCE TO THE DIURIDEAE (ORCHIDACEAE)I MIA MOLVRAy2 AND PAUL J. KORES Department of Biological Sciences, Loyola University, New Orleans, Louisiana 70118 Previous work on seed types within Orchidaceae has demonstrated that characters associated with the seed coat may have considerable phylogenetic utility. Application of the se characters has been complicated in practice by the absence of quan titative descriptors and in some instances by their apparent lack of congruity with the taxa under con sideration. Using quantitative descriptors of size and shape, we have demonstrated that some of the existing seed classes do not represent well delimited, discrete entities, and we have proposed new seed classes to meet these criteria. In the spiranthoid-orchidoid complex, the characters yielding the most clearly delimited shape classes are cell number and variability and degree and stochasticity of medial cell elongation. Of lesser, but still appreciable, significance are the pre sence of varying types and degrees of intercellular gaps, and some, but not all, features of cell walls. Four seed classes are evident on the basis of these characters in Spiranthoideae and Orchidoideae. These seed types are briefly described, and their distribution among the taxa examined for this study is reported. It is hoped that these more strictly delimited seed classes will faci litate phylogenetic analysis in the family. Phylogenetic relationships within the Orchidaceae delimitation of the seed coat characters within the two have been discussed extensively in a series of recent pub putatively most primitive subfamilies of monandrous or lications by Garay (1960, 1972), Dressler (1981, 1986, chids and evaluates the util ity of these characters for the 1990a, b, c, 1993), Rasmussen (1982, 1986), Burns-Bal purpose of phylogenetic inference, extends this avenue of ogh and Funk (1986), and Chase et aI. -
Native Orchid Society of South Australia
NATIVE ORCHID SOCIETY of SOUTH AUSTRALIA NATIVE ORCHID SOCIETY OF SOUTH AUSTRALIA JOURNAL Volume 7, No. 2, March, 1983 Registered by Australia Post Publication No. SBH 1344. Price 40c PATRON: Mr T.R.N. Lothian PRESIDENT: Mr J.T. Simmons SECRETARY: Mr E.R. Hargreaves 4 Gothic Avenue 1 Halmon Avenue STONYFELL S.A. 5066 EVERARD PARK SA 5035 Telephone 32 5070 Telephone 293 2471 297 3724 VICE-PRESIDENT: Mr G.J. Nieuwenhoven COMMITTEE: Mr R. Shooter Mr P. Barnes TREASURER: Mr R.T. Robjohns Mrs A. Howe Mr R. Markwick EDITOR: Mr G.J. Nieuwenhoven NEXT MEETING When: Tuesday 22 March, 1983 at 8.00 p.m. Where: St. Matthews Hall, Bridge Street, Kensington. Subject: First item of the evening will be the proposed changes to the Constitution. Followed by the Annual General Meeting. The normal monthly meeting will take place at the finish of election of officers. One of our own members, Mr Reg Shooter, will speak and show slides on "How I Grow Dendrobiums". If you want to learn how to grow dendrobiums perfectly don't miss this one. ANNUAL GENERAL MEETING NOMINATIONS The following nominations have been received for Committee positions 1983: President: Mr G.J. Nieuwenhoven Vice President: Mr R. Shooter Secretary: Mr R. Hargreaves Treasurer: Mr R. Robjohns Committee: Mrs M. Fuller Mr R. Bates Mr W. Harris Mr R. Barnes still has one year to serve. 12 TUBER BANK REPORT 1982-83 D. Wells An increase in demand for scarcer, Our own club has benefited by tubers less common tubers resulted in the being supplied for raffles, trading quantity per person lower than last table and sales at our own many sell- year, nevertheless most orders were ing outlets at Shows, etc., raising supplied without substitutes. -
Platanthera Chapmanii: Culture, Population Augmentation, and Mycorrhizal Associations
Platanthera chapmanii: culture, population augmentation, and mycorrhizal associations By Kirsten Poff, B.S. A Thesis In Plant and Soil Science Submitted to the Graduate Faculty of Texas Tech University in Partial Fulfillment of the Requirements for the Degree of MASTER OF SCIENCE Approved Dr. Jyotsna Sharma Chair of Committee Dr. Scott Longing Dr. John Zak Dr. Mark Sheridan Dean of the Graduate School August, 2016 © 2016, Kirsten Poff Texas Tech University, Kirsten Poff, August 2016 ACKNOWLEDGEMENTS First I would like to thank my mentor and advisor, Dr. Jyotsna Sharma for all of her help and support. She has challenged and encouraged me throughout my program and the duration of this project. Thanks to her, I am light-years ahead of where I was two years ago. Texas Parks and Wildlife is also gratefully acknowledged for funding portions of this study. I also wish to express my gratitude to Dr. John Zak for his enthusiasm and for encouraging my love of microbes. I also gratefully thank Dr. Scott Longing for his advice, and constructive comments. I sincerely thank all three committee members for all the time and energy they have spent on me throughout the duration of my project. I gratefully acknowledge Dr. Jason Woodward for his encouragement and recommendations as well. I also acknowledge Dr. Cynthia McKenney and Mr. Russel Plowman for their support; I now have a passion for teaching, and a much better understanding of what it is like to teach college level courses. I want to also thank Mr. Robby Carlson for his time and technological assistance. -
Redalyc.ARE OUR ORCHIDS SAFE DOWN UNDER?
Lankesteriana International Journal on Orchidology ISSN: 1409-3871 [email protected] Universidad de Costa Rica Costa Rica BACKHOUSE, GARY N. ARE OUR ORCHIDS SAFE DOWN UNDER? A NATIONAL ASSESSMENT OF THREATENED ORCHIDS IN AUSTRALIA Lankesteriana International Journal on Orchidology, vol. 7, núm. 1-2, marzo, 2007, pp. 28- 43 Universidad de Costa Rica Cartago, Costa Rica Available in: http://www.redalyc.org/articulo.oa?id=44339813005 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative LANKESTERIANA 7(1-2): 28-43. 2007. ARE OUR ORCHIDS SAFE DOWN UNDER? A NATIONAL ASSESSMENT OF THREATENED ORCHIDS IN AUSTRALIA GARY N. BACKHOUSE Biodiversity and Ecosystem Services Division, Department of Sustainability and Environment 8 Nicholson Street, East Melbourne, Victoria 3002 Australia [email protected] KEY WORDS:threatened orchids Australia conservation status Introduction Many orchid species are included in this list. This paper examines the listing process for threatened Australia has about 1700 species of orchids, com- orchids in Australia, compares regional and national prising about 1300 named species in about 190 gen- lists of threatened orchids, and provides recommen- era, plus at least 400 undescribed species (Jones dations for improving the process of listing regionally 2006, pers. comm.). About 1400 species (82%) are and nationally threatened orchids. geophytes, almost all deciduous, seasonal species, while 300 species (18%) are evergreen epiphytes Methods and/or lithophytes. At least 95% of this orchid flora is endemic to Australia. -
Monograph (1953) Ofnothofagus
BLUMEA 29 (1984) 399-408 Miscellaneous botanicalnotes XXVII C.G.G.J.van Steenis J.F. Veldkamp al. , et Rijksherbarium, Leiden, The Netherlands 160. SOME NOTES ON FAGACEAE In thesis B.S. has about the a recent Fey (Zürich) developed a new theory origin of the cupule in Fagaceae. He has concluded that the appendages (spines, lamellae, etc.) on the outside of the cupule are regularly arranged and that they reflect a con- of dichasial flower densation (concrescence) a system, so that cupule and fruit(s) form of together the representation one ancestral inflorescence; the cupular appen- dages would then largely represent the bracts of the ancestral inflorescence. This stands in contrast with former opinions, in which the cupule was interpreted of as separate vegetative origin from the nut(s) which was (were) the remain(s) of the inflorescence. this 'unified' for I cannot agree with hypothesis, which I have given arguments in my monograph (1953) ofNothofagus. In the at the inside of their characteris- Nothofagus stipules carry insertion always tic colleters. Such colleters occur also, though in smaller quantity, at the inside of the cupular appendages, which are, in Nothofagus lamellae. To me they a , represent 'tracer' for the interpretation of their ancestral origin, namely that the cupule is of vegetative origin and the result of a condensation of twigs, a condensed concrescent of of system stipules covering an inner 'lining' a twig. This also readily explains the regularity in the structure of the cupule which in Nothofagus tends to be 4-valved and would with four the distichous agree stipules in rows in phyllotaxis. -
Aliens: the Invasive Species Bulletin Newsletter of the IUCN/SSC Invasive Species Specialist Group
Aliens: The Invasive Species Bulletin Newsletter of the IUCN/SSC Invasive Species Specialist Group ISSN 1173-5988 Issue Number 31, 2011 Coordinator CONTENTS Piero Genovesi, ISSG Chair, ISPRA Editors Editorial pg. 1 Piero Genovesi and Riccardo Scalera News from the ISSG pg. 2 Assistant Editor ...And other news pg. 4 Anna Alonzi Monitoring and control modalities of a honeybee predator, the Yellow Front Cover Photo legged hornet Vespa velutina The yellow-legged hornet Vespa velutina nigrithorax (Hymenoptera: © Photo by Quentin Rome Vespidae) pg. 7 Improving ant eradications: details of more successes, The following people a global synthesis contributed to this issue and recommendations pg. 16 Shyama Pagad, Carola Warner Introduced reindeer on South Georgia – their impact and management pg. 24 Invasive plant species The newsletter is produced twice a year and in Asian elephant habitats pg. 30 is available in English. To be added to the AlterIAS: a LIFE+ project to curb mailing list, or to download the electronic the introduction of invasive version, visit: ornamental plants in Belgium pg. 36 www.issg.org/newsletter.html#Aliens Investigation of Invasive plant Please direct all submissions and other ed- species in the Caucasus: itorial correspondence to Riccardo Scalera current situation pg. 42 [email protected] The annual cost of invasive species to the British economy quantified pg. 47 Published by Eradication of the non-native ISPRA - Rome, Italy sea squirt Didemnum vexillum Graphics design from Holyhead Harbour, Wales, UK pg. 52 Franco Iozzoli, ISPRA Challenges, needs and future steps Coordination for managing invasive alien species Daria Mazzella, ISPRA - Publishing Section in the Western Balkan Region pg. -
The Island Rule and Its Application to Multiple Plant Traits
The island rule and its application to multiple plant traits Annemieke Lona Hedi Hendriks A thesis submitted to the Victoria University of Wellington in partial fulfilment of the requirements for the degree of Master of Science in Ecology and Biodiversity Victoria University of Wellington, New Zealand 2019 ii “The larger the island of knowledge, the longer the shoreline of wonder” Ralph W. Sockman. iii iv General Abstract Aim The Island Rule refers to a continuum of body size changes where large mainland species evolve to become smaller and small species evolve to become larger on islands. Previous work focuses almost solely on animals, with virtually no previous tests of its predictions on plants. I tested for (1) reduced floral size diversity on islands, a logical corollary of the island rule and (2) evidence of the Island Rule in plant stature, leaf size and petiole length. Location Small islands surrounding New Zealand; Antipodes, Auckland, Bounty, Campbell, Chatham, Kermadec, Lord Howe, Macquarie, Norfolk, Snares, Stewart and the Three Kings. Methods I compared the morphology of 65 island endemics and their closest ‘mainland’ relative. Species pairs were identified. Differences between archipelagos located at various latitudes were also assessed. Results Floral sizes were reduced on islands relative to the ‘mainland’, consistent with predictions of the Island Rule. Plant stature, leaf size and petiole length conformed to the Island Rule, with smaller plants increasing in size, and larger plants decreasing in size. Main conclusions Results indicate that the conceptual umbrella of the Island Rule can be expanded to plants, accelerating understanding of how plant traits evolve on isolated islands.