Australian Rhododendron Groups
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A Revision of the Fern Genus Oleandra (Oleandraceae) in Asia 1 Doi: 10.3897/Phytokeys.11.2955 Monograph Launched to Accelerate Biodiversity Research
A peer-reviewed open-access journal PhytoKeys 11: 1–37 (2012)A revision of the fern genus Oleandra (Oleandraceae) in Asia 1 doi: 10.3897/phytokeys.11.2955 MONOGRAPH www.phytokeys.com Launched to accelerate biodiversity research A revision of the fern genus Oleandra (Oleandraceae) in Asia Peter H. Hovenkamp1, Boon-Chuan Ho2 1 Netherlands Centre for Biodiversity Naturalis (section NHN), Leiden University, PO Box 9517, 2300 RA Leiden, The Netherlands 2 Nees-Institut für Biodiversität der Pflanzen, Rheinische Friedrich-Wilhelms- Universität Bonn, Meckenheimer Allee 170, D-53115 Bonn, Germany Corresponding author: Peter H. Hovenkamp ([email protected]) Academic editor: T. Ranker | Received 16 February 2011 | Accepted 29 March 2012 | Published 6 April 2012 Citation: Hovenkamp PH, Ho B-C (2012) A revision of the fern genus Oleandra (Oleandraceae) in Asia. PhytoKeys 11: 1–37. doi: 10.3897/phytokeys.11.2955 Abstract The Asiatic species of Oleandra (Oleandraceae) are revised. We reduce a large number of species to O. neriiformis and O. sibbaldii, we provide a revised circumscription of O. cumingii and O. undulata and we establish the identity of O. vulpina. In total, we recognize 9 species, with full synonymy, descriptions and distribution maps. A list of identifications is appended. Keywords Oleandra, systematics Introduction Virtually all authors who have dealt with the genus Oleandra Cav. have commented on its distinctness or naturalness. The shrubby growth form, particularly distinct in O. neriiformis Cav., prompted Cavanilles (1799; 1802) not only to derive the genus name, but also the species name from Nerium oleander L. (Apocynaceae). From this it should be clear that he saw the aerial stems of Oleandra neriiformis, of which the forms with distinctly whorled fronds are indeed strongly reminiscent of branches of Nerium olean- der. -
Brooklyn, Cloudland, Melsonby (Gaarraay)
BUSH BLITZ SPECIES DISCOVERY PROGRAM Brooklyn, Cloudland, Melsonby (Gaarraay) Nature Refuges Eubenangee Swamp, Hann Tableland, Melsonby (Gaarraay) National Parks Upper Bridge Creek Queensland 29 April–27 May · 26–27 July 2010 Australian Biological Resources Study What is Contents Bush Blitz? Bush Blitz is a four-year, What is Bush Blitz? 2 multi-million dollar Abbreviations 2 partnership between the Summary 3 Australian Government, Introduction 4 BHP Billiton and Earthwatch Reserves Overview 6 Australia to document plants Methods 11 and animals in selected properties across Australia’s Results 14 National Reserve System. Discussion 17 Appendix A: Species Lists 31 Fauna 32 This innovative partnership Vertebrates 32 harnesses the expertise of many Invertebrates 50 of Australia’s top scientists from Flora 62 museums, herbaria, universities, Appendix B: Threatened Species 107 and other institutions and Fauna 108 organisations across the country. Flora 111 Appendix C: Exotic and Pest Species 113 Fauna 114 Flora 115 Glossary 119 Abbreviations ANHAT Australian Natural Heritage Assessment Tool EPBC Act Environment Protection and Biodiversity Conservation Act 1999 (Commonwealth) NCA Nature Conservation Act 1992 (Queensland) NRS National Reserve System 2 Bush Blitz survey report Summary A Bush Blitz survey was conducted in the Cape Exotic vertebrate pests were not a focus York Peninsula, Einasleigh Uplands and Wet of this Bush Blitz, however the Cane Toad Tropics bioregions of Queensland during April, (Rhinella marina) was recorded in both Cloudland May and July 2010. Results include 1,186 species Nature Refuge and Hann Tableland National added to those known across the reserves. Of Park. Only one exotic invertebrate species was these, 36 are putative species new to science, recorded, the Spiked Awlsnail (Allopeas clavulinus) including 24 species of true bug, 9 species of in Cloudland Nature Refuge. -
Mountain Laurel Or Rhododendron? Recreation Area Vol
U.S. Dept. of the Interior National Park Service . Spanning the Gap The newsletter of Delaware Water Gap National Mountain Laurel or Rhododendron? Recreation Area Vol. 7 No. 2 Summer 1984 These two members of the plant kingdom are often confused. Especially before they blossom, they resemble each other with their bushy appearance and long, dark-green leaves. Both plants ARE shrubs, and they are often seen growing together. Another thing they have in common: although some species have not been proven dangerous, it is well to consider ALL members of the laurel- (Above) Rhodendron. rhododendron-azalea group of plants as potentially toxic. The rhododendron (rhododenron maximum) is undoubtedly the most conspicuous understory plant in the mountain forests of Pennsylvania. In ravines and hollows and along shaded watercourses it often grows so luxuriantly as to form almost impenetrable tangles. In June or early July, large clusters of showy blossoms, ranging from white to light rosy- pink, appear at the ends of the branchlets. People travel many miles to witness the magnificent show which is provided by the rhododendron at flowering time. In the southern Appalachians the plant grows much larger than it ordinarily does in this area, often becoming a tree 25 feet or more in height. The dense thickets of rhododendron in the stream valleys and on the lower slopes of our mountains are favorite yarding grounds for deer when the Rhodendron. snows become deep in the wintertime. The dark- green, leathery leaves react to subfreezing temperatures by bending downward and rolling into a tight coil. Although the shrub is often browsed to excess, it has little or no nutritional value. -
Dendrobium Kingianum Bidwill Ex Lindl
Volume 24: 203–232 ELOPEA Publication date: 19 May 2021 T dx.doi.org/10.7751/telopea14806 Journal of Plant Systematics plantnet.rbgsyd.nsw.gov.au/Telopea • escholarship.usyd.edu.au/journals/index.php/TEL • ISSN 0312-9764 (Print) • ISSN 2200-4025 (Online) A review of Dendrobium kingianum Bidwill ex Lindl. (Orchidaceae) with morphological and molecular- phylogenetic analyses Peter B. Adams1,2, Sheryl D. Lawson2, and Matthew A.M. Renner 3 1The University of Melbourne, School of BioSciences, Parkville 3010, Victoria 2National Herbarium of Victoria, Royal Botanic Gardens Victoria, Birdwood Ave., Melbourne 3004, Victoria 3National Herbarium of New South Wales, Royal Botanic Gardens and Domain Trust, Sydney 2000, New South Wales Author for correspondence: [email protected] Abstract Populations of Dendrobium kingianum Bidwill ex Lindl. from near Newcastle, New South Wales to southern and central west Queensland and encompassing all regions of the distribution were studied using field observations, morphometric analysis and nrITS sequences. A total of 281 individuals were used to construct regional descriptions of D. kingianum and 139 individuals were measured for 19 morphological characters, and similarities and differences among specimens summarised using multivariate statistical methods. Patterns of morphological variation within D. kingianum are consistent with a single variable species that expresses clinal variation, with short-growing plants in the south and taller plants in the northern part of the distribution. The nrITS gene tree suggests two subgroups within D. kingianum subsp. kingianum, one comprising northern, the other southern individuals, which may overlap in the vicinity of Dorrigo, New South Wales. The disjunct D. kingianum subsp. carnarvonense Peter B. -
Diversity of Fungal Assemblages in Roots of Ericaceae in Two
Diversity of fungal assemblages in roots of Ericaceae in two Mediterranean contrasting ecosystems Ahlam Hamim, Lucie Miche, Ahmed Douaik, Rachid Mrabet, Ahmed Ouhammou, Robin Duponnois, Mohamed Hafidi To cite this version: Ahlam Hamim, Lucie Miche, Ahmed Douaik, Rachid Mrabet, Ahmed Ouhammou, et al.. Diversity of fungal assemblages in roots of Ericaceae in two Mediterranean contrasting ecosystems. Comptes Rendus Biologies, Elsevier Masson, 2017, 340 (4), pp.226-237. 10.1016/j.crvi.2017.02.003. hal- 01681523 HAL Id: hal-01681523 https://hal.archives-ouvertes.fr/hal-01681523 Submitted on 23 Apr 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/315062117 Diversity of fungal assemblages in roots of Ericaceae in two Mediterranean contrasting ecosystems Article in Comptes rendus biologies · March 2017 DOI: 10.1016/j.crvi.2017.02.003 CITATIONS READS 0 37 7 authors, including: Ahmed Douaik Rachid Mrabet Institut National de Recherche Agronomique -
Phylogenetic Diversity of Ferns Reveals Different Patterns of Niche Conservatism and Habitat Filtering Between Epiphytic and Terrestrial Assemblages†
a Frontiers of Biogeography 2021, 13.3, e50023 Frontiers of Biogeography RESEARCH ARTICLE the scientific journal of the International Biogeography Society Phylogenetic diversity of ferns reveals different patterns of niche conservatism and habitat filtering between epiphytic and terrestrial assemblages† Adriana C. Hernández-Rojas1* , Jürgen Kluge1 , Sarah Noben2 , Johan D. Reyes Chávez3 , Thorsten Krömer4 , César I. Carvajal-Hernández5 , Laura Salazar6 and Michael Kessler2 1 Faculty of Geography, Philipps University Marburg, Germany; 2 Systematic and Evolutionary Botany, University of Zurich, Switzerland; 3 Escuela Agrícola Panamericana Zamorano, Centro Zamorano de Biodiversidad, Carrera de Ambiente y Desarrollo, Valle de Yeguare, Francisco Morazán, Honduras; 4 Centro de Investigaciones Tropicales (CITRO), Universidad Veracruzana, México; 5 Instituto de Investigaciones Biológicas, Universidad Veracruzana, México;6 Centro de Investigación de la Biodiversidad y Cambio Climático e Ingeniería en Biodiversidad y Recursos Genéticos, Facultad de Ciencias del Medio Ambiente, Universidad Tecnológica Indoamérica, Machala y Sabanilla, Quito, Ecuador. *Corresponding author: Adriana C. Hernández-Rojas, [email protected], [email protected] This paper is part of an Elevational Gradients and Mountain Biodiversity Special Issue. Abstract Highlights Much attention has been directed to understanding • Epiphytic and terrestrial fern assemblages across species richness patterns, but adding an evolutionary elevational and latitudinal -
Newsletter No
Newsletter No. 167 June 2016 Price: $5.00 AUSTRALASIAN SYSTEMATIC BOTANY SOCIETY INCORPORATED Council President Vice President Darren Crayn Daniel Murphy Australian Tropical Herbarium (ATH) Royal Botanic Gardens Victoria James Cook University, Cairns Campus Birdwood Avenue PO Box 6811, Cairns Qld 4870 Melbourne, Vic. 3004 Australia Australia Tel: (+61)/(0)7 4232 1859 Tel: (+61)/(0) 3 9252 2377 Email: [email protected] Email: [email protected] Secretary Treasurer Leon Perrie John Clarkson Museum of New Zealand Te Papa Tongarewa Queensland Parks and Wildlife Service PO Box 467, Wellington 6011 PO Box 975, Atherton Qld 4883 New Zealand Australia Tel: (+64)/(0) 4 381 7261 Tel: (+61)/(0) 7 4091 8170 Email: [email protected] Mobile: (+61)/(0) 437 732 487 Councillor Email: [email protected] Jennifer Tate Councillor Institute of Fundamental Sciences Mike Bayly Massey University School of Botany Private Bag 11222, Palmerston North 4442 University of Melbourne, Vic. 3010 New Zealand Australia Tel: (+64)/(0) 6 356- 099 ext. 84718 Tel: (+61)/(0) 3 8344 5055 Email: [email protected] Email: [email protected] Other constitutional bodies Hansjörg Eichler Research Committee Affiliate Society David Glenny Papua New Guinea Botanical Society Sarah Matthews Heidi Meudt Advisory Standing Committees Joanne Birch Financial Katharina Schulte Patrick Brownsey Murray Henwood David Cantrill Chair: Dan Murphy, Vice President Bob Hill Grant application closing dates Ad hoc adviser to Committee: Bruce Evans Hansjörg Eichler Research -
Pdf/A (670.91
Phytotaxa 164 (1): 001–016 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ Article PHYTOTAXA Copyright © 2014 Magnolia Press ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.164.1.1 On the monophyly of subfamily Tectarioideae (Polypodiaceae) and the phylogenetic placement of some associated fern genera FA-GUO WANG1, SAM BARRATT2, WILFREDO FALCÓN3, MICHAEL F. FAY4, SAMULI LEHTONEN5, HANNA TUOMISTO5, FU-WU XING1 & MAARTEN J. M. CHRISTENHUSZ4 1Key Laboratory of Plant Resources Conservation and Sustainable Utilization, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou 510650, China. E-mail: [email protected] 2School of Biological and Biomedical Science, Durham University, Stockton Road, Durham, DH1 3LE, United Kingdom. 3Institute of Evolutionary Biology and Environmental Studies, University of Zurich, Winterthurerstrasse 190, 8075 Zurich, Switzerland. 4Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 4DS, United Kingdom. E-mail: [email protected] (author for correspondence) 5Department of Biology, University of Turku, FI-20014 Turku, Finland. Abstract The fern genus Tectaria has generally been placed in the family Tectariaceae or in subfamily Tectarioideae (placed in Dennstaedtiaceae, Dryopteridaceae or Polypodiaceae), both of which have been variously circumscribed in the past. Here we study for the first time the phylogenetic relationships of the associated genera Hypoderris (endemic to the Caribbean), Cionidium (endemic to New Caledonia) and Pseudotectaria (endemic to Madagascar and Comoros) using DNA sequence data. Based on a broad sampling of 72 species of eupolypods I (= Polypodiaceae sensu lato) and three plastid DNA regions (atpA, rbcL and the trnL-F intergenic spacer) we were able to place the three previously unsampled genera. -
Rosebay Rhododendron Rhododendron Maximum
SUMMER 2004, VOLUME 5, ISSUE 3 NEWSLETTER OF THE NORTH AMERICAN NATIVE PLANT SOCIETY Native Plant to Know Rosebay rhododendron Rhododendron maximum by Kevin Kavanagh Joyce Kilmer Memorial Forest, tucked away inside the Nantahala National Forest RANTON of North Carolina’s Appalachian G Mountains, is one of those RIGITTE North American pil- B grimages that all botanists should make at least once in ILLUSTRATION BY their lives.As a graduate student in for- est ecology, I had read about it in the scientific literature, one of the best examples of an old-growth ‘cove’ forest on the continent: massive tulip trees (Lirio- dendron tulipifera) more than 500 years old, east- ern hemlocks (Tsuga canadensis) rivalling their large elliptic leaves forming a delicate pat- Appalachian chain.Although hardy in eastern their west-coast tern against the bright yellows of overstorey Canadian gardens, Rhododendron maximum rainforest cousins tulip trees in peak autumn coloration.Along does not penetrate naturally into Canada. in size and age, mountain streams, the trails wove in among While there are historical accounts from and, along the expansive rhododendron thickets that in Ontario, Quebec, New Brunswick and Nova streams, dense under- places rose more than 10 metres (30 feet) over- Scotia, none of them, to my knowledge, have storey stands of rosebay rhododendrons head on gnarled stems (trunks!), the largest of been authenticated. (Rhododendron maximum) forming a dark which were close to 30 centimetres (one foot) In its native range, rosebay rhododendron canopy overhead. in diameter. (also known as great-laurel or great rhododen- To call it a canopy is not embellishment. -
Rhododendron Glenn Dale Hybrid Azaleas
U.S. National Arboretum Plant Introduction Rhododendron Glenn Dale Hybrid Azaleas Nothing says spring like azaleas! One of the National Arboretum’s most popular plantings, the Glenn Dale Azaleas draw thousands for annual spring viewing. Horticulturist Benjamin Y. Mor- rison worked for over 25 years to create this superior group of winter-hardy azaleas with large, colorful flowers suitable for the Washington, DC region. We present a small vignette of the 454 named introductions to entice you to grow these lovely spring treasures. Check our on-line photo gallery and be sure to make an April visit to the Arboretum part of your tradition too! The south face of Mt. Hamilton at the National Arboretum in Washington, DC was planted with approximately 15,000 azaleas from Glenn Dale in 1946-47. In 1949, the Arboretum opened to the public for the first time during the azalea bloom. U.S. National Arboretum Plant Introduction U.S. Department of Agriculture, Agricultural Research Service, 3501 New York Ave., N.E., Washington, DC 20002 Glenn Dale Hybrid Azaleas Botanical Name: Rhododendron Glenn Dale hybrids Plants in the Glenn Dale azalea breeding program were initially assigned Bell or "B" numbers an old name for the Plant Introduction Station at Glenn Dale, MD. Plant Introduction (PI) numbers were assigned later. The first “B” number was assigned to ‘Dimity’ in 1937. and ‘Satrap’ received the last “ B” number in 1951 and PI number in 1952. Family Ericaceae Hardiness: U.S.D.A. Zones 6b-8 (some hardy to Zone 5) Development: In the late 1920’s B.Y. -
Figure 1: Afrothismia Korupensis Sainge & Franke Afrothismia
Figure 1: Afrothismia korupensis Sainge & Franke Afrothismia fungiformis Sainge, Kenfack & Afrothismia pusilla Sainge, Kenfack & Chuyong (in press) Chuyong (in press) Afrothismia sp.nov. Three new species of Afrothismia discovered during this study. CASESTUDY: SYSTEMATICS AND ECOLOGY OF THISMIACEAE IN CAMEROON BY SAINGE NSANYI MOSES AN MSC THESIS PRESENTED TO THE DEPARTMENT OF BOTANY AND PLANT PHYSIOLOGY, UNIVERSITY OF BUEA, CAMEROON 1.0. INTRODUCTION The family Thismiaceae Agardh comprises five genera Afrothismia Schltr., Haplothismia Airy Shaw, Oxygyne Schltr., Thismia Griff. and Tiputinia P. E. Berry & C. L. Woodw. (Merckx 2006, Woodward et al., 2007) with close to 63 - 90 species (Vincent et al. 2013, Sainge et al. 2012). The worldwide distribution of this family ranges from lowland rain forest and sub-montane forest of South America, Asia and Africa, with a few species in the temperate forest of Australia, New Zealand, and Japan to the upper mid-western U.S.A., on an evergreen, semi-deciduous and deciduous vegetation type. In tropical Africa, they occur in two genera (Afrothismia Schltr. & Oxygyne Schltr.) with about 20 species with the highest diversity in the forest of Central Africa (Cheek 1996, Franke 2004, 2005, Sainge et al., 2005, 2010 and Sainge et al. 2012). The recent taxonomic Classification of Thismiaceae (Merckx et al. 2006) is as follows: Kingdom: Plantae Division: Magnoliophyta Class: Magnoliopsida Order: Dioscoreales Family: Thismiaceae Genera: Afrothismia Schltr., Haplothismia Airy Shaw, Oxygyne Schltr., Thismia Griff. and Tiputinia Berry & Woodward In tropical Africa, thismiaceae was discovered over a century ago but classified as Burmanniaceae (Engler, 1905). This family is monocotyledonous, and form part of a heterogeneous group of plants known as the myco-heterotrophic plants (MHPs) (Leake, 1994) consisting of nine plant families: Petrosaviaceae, Polygalaceae, Ericaceae, Iridaceae (Geosiris), Thismiaceae, Burmanniaceae, Triuridaceae, Gentianaceae and some terrestrial Orchidaceae. -
Ericaceae Root Associated Fungi Revealed by Culturing and Culture – Independent Molecular Methods
a Ericaceae root associated fungi revealed by culturing and culture – independent molecular methods. by Damian S. Bougoure BSc (Hons) Thesis submitted in accordance with the requirements for the degree of Doctor of Philosophy Centre for Horticulture and Plant Sciences University of Western Sydney February 2006 2 ACKNOWLEDGEMENTS Although I am credited with writing this thesis there is a multitude of people that have contributed to its completion in ways other than hitting the letters on a keyboard and I would like to thank them here. Firstly I’d like to thank my supervisor, Professor John Cairney, whose knowledge and guidance was invaluable in steering me along the PhD path. The timing of John’s ‘motivational chats’ was uncanny and his patience particularly, during the writing stage, seemed limitless at times. I’d also like to thank the Australian government for granting me an Australian Postgraduate Award (APA) scholarship, Paul Worden from Macquarie University and the staff from the Millennium Institute at Westmead Hospital for performing DNA sequencing and the National Parks and Wildlife Service of New South Wales and Environmental Protection agency of Queensland for permission to collect the Ericaceae plants. Thankyou to Mary Gandini from James Cook University for showing me the path to a Rhododendron lochiae population through the thick North Queenland rainforest. Without her help and I’d still be pointing the GPS at the sky. Thankyou to the other people in the lab studying mycorrhizas including Catherine Hitchcock, Susan Chambers, Adrienne Williams and particularly Brigitte Bastias with whom I shared an office. Everyone mentioned was generally just as willing as I was to talk about matters other than mycorrhizas.