NZ Indigenous Vascular Plant Checklist
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Insects of Macquarie Island. Introduction1
Pacific Insects 4 (4) : 905-915 December, 15, 1962 INSECTS OF MACQUARIE ISLAND. INTRODUCTION1 By J. Linsley Gressitt BISHOP MUSEUM, HONOLULU Abstract: Collections of land arthropods were made on Macquarie Island by J. L. Gres sitt and J. H. Calaby, 4-10 December 1960, and by Keith Watson, December 1960-Decem- ber 1961. This paper is a brief discussion of the geography and environment of Macquarie, introductory to the systematic papers describing the fauna. Watson, of the Australian Na tional Antarctic Research Expeditions, will later publish his general ecological studies, when the species are all identified. INTRODUCTION This paper is a brief description of the geography and environment of Macquarie Is land, as related to land arthropods. It is presented by way of introduction to the series of reports by various specialists on the land arthropod fauna of the island. The bulk of these reports immediately follow this article. (One Macquarie mite is discussed in the third of the preceding articles by Wallwork on Antarctic mites, and another is mentioned in his second article.) Others will appear in later issues, when they are completed. After publication of the bulk of these taxonomic reports, Keith Watson will publish his general report on the land arthropod fauna of Macquarie, incorporating his ecological studies on the fauna. Through the kindness of Mr. P. G. Law, Director of the Antarctic Division, Australian Department of External Affairs, I was permitted to join the Australian National Antarctic Research Expedition for the annual resupply trip to Macquarie Island in early December 1960. The operation, supported by the chartered Danish ice-breaker Magga Dan, was car ried on at Macquarie from 4th to lOth December. -
Bio 308-Course Guide
COURSE GUIDE BIO 308 BIOGEOGRAPHY Course Team Dr. Kelechi L. Njoku (Course Developer/Writer) Professor A. Adebanjo (Programme Leader)- NOUN Abiodun E. Adams (Course Coordinator)-NOUN NATIONAL OPEN UNIVERSITY OF NIGERIA BIO 308 COURSE GUIDE National Open University of Nigeria Headquarters 14/16 Ahmadu Bello Way Victoria Island Lagos Abuja Office No. 5 Dar es Salaam Street Off Aminu Kano Crescent Wuse II, Abuja e-mail: [email protected] URL: www.nou.edu.ng Published by National Open University of Nigeria Printed 2013 ISBN: 978-058-434-X All Rights Reserved Printed by: ii BIO 308 COURSE GUIDE CONTENTS PAGE Introduction ……………………………………......................... iv What you will Learn from this Course …………………............ iv Course Aims ……………………………………………............ iv Course Objectives …………………………………………....... iv Working through this Course …………………………….......... v Course Materials ………………………………………….......... v Study Units ………………………………………………......... v Textbooks and References ………………………………........... vi Assessment ……………………………………………….......... vi End of Course Examination and Grading..................................... vi Course Marking Scheme................................................................ vii Presentation Schedule.................................................................... vii Tutor-Marked Assignment ……………………………….......... vii Tutors and Tutorials....................................................................... viii iii BIO 308 COURSE GUIDE INTRODUCTION BIO 308: Biogeography is a one-semester, 2 credit- hour course in Biology. It is a 300 level, second semester undergraduate course offered to students admitted in the School of Science and Technology, School of Education who are offering Biology or related programmes. The course guide tells you briefly what the course is all about, what course materials you will be using and how you can work your way through these materials. It gives you some guidance on your Tutor- Marked Assignments. There are Self-Assessment Exercises within the body of a unit and/or at the end of each unit. -
Nzbotsoc No 107 March 2012
NEW ZEALAND BOTANICAL SOCIETY NEWSLETTER NUMBER 107 March 2012 New Zealand Botanical Society President: Anthony Wright Secretary/Treasurer: Ewen Cameron Committee: Bruce Clarkson, Colin Webb, Carol West Address: c/- Canterbury Museum Rolleston Avenue CHRISTCHURCH 8013 Subscriptions The 2012 ordinary and institutional subscriptions are $25 (reduced to $18 if paid by the due date on the subscription invoice). The 2012 student subscription, available to full-time students, is $12 (reduced to $9 if paid by the due date on the subscription invoice). Back issues of the Newsletter are available at $7.00 each. Since 1986 the Newsletter has appeared quarterly in March, June, September and December. New subscriptions are always welcome and these, together with back issue orders, should be sent to the Secretary/Treasurer (address above). Subscriptions are due by 28 February each year for that calendar year. Existing subscribers are sent an invoice with the December Newsletter for the next years subscription which offers a reduction if this is paid by the due date. If you are in arrears with your subscription a reminder notice comes attached to each issue of the Newsletter. Deadline for next issue The deadline for the June 2012 issue is 25 May 2012. Please post contributions to: Lara Shepherd Museum of New Zealand Te Papa Tongarewa P.O. Box 467 Wellington Send email contributions to [email protected]. Files are preferably in MS Word, as an open text document (Open Office document with suffix “.odt”) or saved as RTF or ASCII. Macintosh files can also be accepted. Graphics can be sent as TIF JPG, or BMP files; please do not embed images into documents. -
The Smut Fungi (Ustilaginomycetes) of Restionaceae S. Lat
MYCOLOGIA BALCANICA 3: 19–46 (2006) 19 Th e smut fungi (Ustilaginomycetes) of Restionaceae s. lat. Kálmán Vánky Herbarium Ustilaginales Vánky (H.U.V.), Gabriel-Biel-Str. 5, D-72076 Tübingen, Germany (e-mail: [email protected]) Received 2 October 2005 / Accepted 25 October 2005 Abstract. Smut fungi of Restionaceae s. lat. were studied. Th ey are classifi ed into two genera, Restiosporium and Websdanea. Problems of species delimitation in these smuts are discussed. In addition to the nine known smut fungi, thirteen new species are described and illustrated: Restiosporium anarthriae, R. apodasmiae, R. chaetanthi, R. desmocladii, R. eurychordae, R. fl exuosum, R. hypolaenae, R. lepyrodiae, R. pallentis, R. patei, R. proliferum, R. spathacei, and R. sphacelatum. Key words: new species, Restionaceae s. lat., Restiosporium, smut fungi, taxonomy, Websdanea Introduction and stained in 1 % aqueous uranyl acetate for 1 h in the dark. After fi ve washes in distilled water, the material was Th e monocotyledonous Restionaceae is a remarkable family dehydrated in acetone series, embedded in Spurr’s plastic, of Southern Hemisphere, evergreen, rush-like plants. Th ey and sectioned with a diamond knife. Semi-thin sections are concentrated mainly in SW Africa and in SW Australia. were stained with new fuchsin and crystal violet, mounted Th e c. 320 species of African Restionaceae, in 19 genera, were in ‘Entellan’ and studied in a light microscope. revised by Linder (1985, 1991). Th e 170 species of Australian Spore ball and spore morphology was studied using Restionaceae s. lat. were published by Meney & Pate (1999) a light microscope (LM) with an oil immersion lens at a in a beautifully illustrated monograph. -
Low Risk Aquarium and Pond Plants
Plant Identification Guide Low-risk aquarium and pond plants Planting these in your pond or aquarium is environmentally-friendly. Glossostigma elatinoides, image © Sonia Frimmel. One of the biggest threats to New Zealand’s waterbodies is the establishment and proliferation of weeds. The majority of New Zealand’s current aquatic weeds started out as aquarium and pond plants. To reduce the occurrence of new weeds becoming established in waterbodies this guide has been prepared to encourage the use of aquarium and pond plants that pose minimal risk to waterbodies. Guide prepared by Dr John Clayton, Paula Reeves, Paul Champion and Tracey Edwards, National Centre of Aquatic Biodiversity and Biosecurity, NIWA with funding from the Department of Conservation. The guides will be updated on a regular basis and will be available on the NIWA website: www.niwa.co.nz/ncabb/tools. Key to plant life-forms Sprawling marginal plants. Grow across the ground and out over water. Pond plants Short turf-like plants. Grow in shallow water on the edges of ponds and foreground of aquariums. Includes very small plants (up to 2-3 cm in height). Most species can grow both submerged (usually more erect) and emergent. Pond and aquarium plants Tall emergent plants. Can grow in water depths up to 2 m deep depending on the species. Usually tall reed-like plants but sometimes with broad leaves. Ideal for deeper ponds. Pond plants Free floating plants. These plants grow on the water surface and are not anchored to banks or bottom substrates. Pond and aquarium plants Floating-leaved plants. Water lily-type plants. -
1999 New Zealand Botanical Society
NEW ZEALAND BOTANICAL SOCIETY NEWSLETTER NUMBER 57 SEPTEMBER 1999 New Zealand Botanical Society President: Jessica Beever Secretary/Treasurer: Anthony Wright Committee: Bruce Clarkson, Colin Webb, Carol West Address: c/- Canterbury Museum Rolleston Avenue CHRISTCHURCH 8001 NEW ZEALAND Subscriptions The I999 ordinary and institutional subs are $18 (reduced to $15 if paid by the due date on the subscription invoice). The 1999 student sub, available to full-time students, is $9 (reduced to $7 if paid by the due date on the subscription invoice). Back issues of the Newsletter are available at $2.50 each from Number 1 (August 1985) to Number 46 (December 1996), $3.00 each from Number 47 (March 1997) to Number 50 (December 1997), and $3.75 each from Number 51 (March 1998) onwards. Since 1986 the Newsletter has appeared quarterly in March, June, September and December. New subscriptions are always welcome and these, together with back issue orders, should be sent to the Secretary/Treasurer (address above). Subscriptions are due by 28 February of each year for that calendar year. Existing subscribers are sent an invoice with the December Newsletter for the next year's subscription which offers a reduction if this is paid by the due date. If you are in arrears with your subscription a reminder notice comes attached to each issue of the Newsletter. Deadline for next issue The deadline for the December 1999 issue (Number 58) is 26 November 1999. Please forward contributions to: Dr Carol J. West, c/- Department of Conservation PO Box 743 Invercargill Contributions may be provided on an IBM compatible floppy disc (Word) or by e-mail to [email protected] Cover Illustration Plagiochila ramosissima with antheridial branches. -
Ecology of the Olearia Colensoi Dominated Sub-Alpine Scrub in the Southern Ruahine Range, New Zealand
Copyright is owned by the Author of the thesis. Permission is given for a copy to be downloaded by an individual for the purpose of research and private study only. The thesis may not be reproduced elsewhere without the permission of the Author. 581 .509 9355 Ess ECOLOGY OF THE OLEARIA COLENSOI DOMINATED SUB-ALPINE SCRUB IN THE SOUTHERN RUAHINE RANGE, NEW ZEALAND. A thesis presented in partial fulfilment of the requirements for the degree of Master of Science in Botany at Massey University New Zealand Peter Ronald van Essen 1992 Olearia colensoi in flower. Reproduced from a lithograph by Walter Fitch in Flora Novae-Zelandiae (J.D. Hooker 1852). Source: Alexander Turnbull Library in New Zealand Heritage, Paul Hamlyn Ltd ABSTRACT The Olearia colensoi (leatherwood or tupari) dominated southern Ruahine sub-alpine scrub is the largest continuous area of sub-alpine asteraceous scrub in New Zealand - the result of a lowered treeline due to climatic conditions characterised by high cloud cover, high rainfall, and high winds and the absence of high altitude Nothofagus species. Meteorological investigation of seven sites in the southern Ruahine found that altitude alone was the main environmental detenninant of climatic variation, particularly temperature regime. Temperatures varied between sites at a lapse rate of 0.61°C lOOm-1 while daily fluctuation patterns were uniform for all sites. Rainfall increased with altitude over the Range-at a rate of 3.8mm m-1. Cloud interception, unrecorded by standard rain gauges, adds significantly to total 'rainfall'. Vegetative phenology of Olearia colensoi is highly seasonal and regular with an annual growth flush from mid November to January. -
BSBI News Index 121-130 ABC 8Pt FINAL
BSBI News INDEX to Nos 121 – 130 September 2012 to September 2015 Compiled by GWYNN ELLIS ISSN 2397-8813 1 GUIDE TO THE INDEX ABBREVIATIONS AEM Annual Exhibition Meeting Illus. Illustration AGM Annual General Meeting Infl. Inflorescence ASM Annual Summer Meeting Lvs Leaves cf. confer (compare) photo © photo copyright holder congrats congratulations Rev. Review CS Colour Section Rpt Report del. delineavit (drawn) s.l. sensu lato (broad sense) Descr. Description s.s. sensu stricto (narrow sense) Diag. Diagram v.c. vice-county Exbn Exhibition v.cc. vice-counties Exbt Exhibit (♀) female parent Fld Mtg Rpt Field Meeting Report (♂) male parent Fls Flowers ACKNOWLEDGEMENTS: The compiler wishes to thank David Pearman for much helpful advice and for scrutinising the final text. However, responsibility for checking the index and its final form rests solely with the compiler. BOOKS et al. are italicised as are Periodicals and scientific names COLOUR PAGES: In the index all colour page numbers are distinguished by being underlined with the cover pages enclosed in square brackets [ ]. The front cover and inside front cover are numbered [i] and [ii] respectively while the inside back and back cover pages are numbered according to the number of pages, thus with an issue of 76 pages the inside back cover is [77] and the back cover [78]. Colour Section plates are numbered CS1, CS2, CS3, CS4. Photographers are now indexed by name with the qualification (photo ©) COMPILATION: Using the original text on computer, the entries for each issue were generated by deleting all unwanted text. After checking, the entries were then sorted into alphabetical order, condensed, and finally output as pdf files for the Printer. -
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. -
Marginal Evidence for Taro Production in Northern New Zealand
LETTER REPLY TO BARBER: Marginal evidence for taro production in northern LETTER New Zealand between 1200 and 1500 CE Matthew Prebblea,1, Atholl J. Andersona, Paul Augustinusb, Joshua Emmittc, Stewart J. Fallond, Louise L. Fureye, Simon J. Holdawayc, Alex Jorgensenc, Thegn N. Ladefogedc,f, Peter J. Matthewsg, Jean-Yves Meyerh, Rebecca Phillippsc, Rod Wallacec, and Nicholas Porchi We welcome Barber’s (1) comments and are grateful for not meet widely accepted criteria for high-precision the opportunity to respond. Our study of wetland taro dating, as they contain mixed carbon sources (9). (Colocasia esculenta) gardens during the initial coloni- 3) Description of crop ecosystems: Ancient crop ecosys- zation period (ICP) (1200 to 1500 CE) in New Zealand tems cannot be described without comprehensive did not overlook the evidence from the Aupouri Penin- analyses of biological remains from archaeological sula (2–4). We agree that gardens were probably estab- contexts. At Polynesian arrival, the Motutangi wet- lished on mainland New Zealand, within the climate lands were dominated by the large-statured conifer envelope shown in figure 1 of our paper (4), but in areas Dacrydium cupressinum, requiring repeated firing to that lacked large-statured forests at Polynesian arrival. establish gardens, and Restionaceae (3), most likely However, the fossil evidence from Motutangi does not Apodasmia similis, a rush which dominates the mar- meet the 3 criteria for defining ICP taro gardens met in gins of regularly flooded estuaries or lakes and out- our study of Ahuahu and subtropical French Polynesia: competes other plants in nutrient-poor soils (10). This densely spreading rush likely posed difficulties for 1) Reliable fossil proxies: We identify pollen, the crop cultivation, although taro may have been com- most reliable fossil proxy for taro (5), but also clus- petitive if grown in clumps over multiple sea- ters of small globular orbicular starch grains inside sons. -
Poaceae: Pooideae) Based on Plastid and Nuclear DNA Sequences
d i v e r s i t y , p h y l o g e n y , a n d e v o l u t i o n i n t h e monocotyledons e d i t e d b y s e b e r g , p e t e r s e n , b a r f o d & d a v i s a a r h u s u n i v e r s i t y p r e s s , d e n m a r k , 2 0 1 0 Phylogenetics of Stipeae (Poaceae: Pooideae) Based on Plastid and Nuclear DNA Sequences Konstantin Romaschenko,1 Paul M. Peterson,2 Robert J. Soreng,2 Núria Garcia-Jacas,3 and Alfonso Susanna3 1M. G. Kholodny Institute of Botany, Tereshchenkovska 2, 01601 Kiev, Ukraine 2Smithsonian Institution, Department of Botany MRC-166, National Museum of Natural History, P.O. Box 37012, Washington, District of Columbia 20013-7012 USA. 3Laboratory of Molecular Systematics, Botanic Institute of Barcelona (CSIC-ICUB), Pg. del Migdia, s.n., E08038 Barcelona, Spain Author for correspondence ([email protected]) Abstract—The Stipeae tribe is a group of 400−600 grass species of worldwide distribution that are currently placed in 21 genera. The ‘needlegrasses’ are char- acterized by having single-flowered spikelets and stout, terminally-awned lem- mas. We conducted a molecular phylogenetic study of the Stipeae (including all genera except Anemanthele) using a total of 94 species (nine species were used as outgroups) based on five plastid DNA regions (trnK-5’matK, matK, trnHGUG-psbA, trnL5’-trnF, and ndhF) and a single nuclear DNA region (ITS). -
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