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Summary of Offerings in the PBS Bulb Exchange, Dec 2012- Nov 2019
Summary of offerings in the PBS Bulb Exchange, Dec 2012- Nov 2019 3841 Number of items in BX 301 thru BX 463 1815 Number of unique text strings used as taxa 990 Taxa offered as bulbs 1056 Taxa offered as seeds 308 Number of genera This does not include the SXs. Top 20 Most Oft Listed: BULBS Times listed SEEDS Times listed Oxalis obtusa 53 Zephyranthes primulina 20 Oxalis flava 36 Rhodophiala bifida 14 Oxalis hirta 25 Habranthus tubispathus 13 Oxalis bowiei 22 Moraea villosa 13 Ferraria crispa 20 Veltheimia bracteata 13 Oxalis sp. 20 Clivia miniata 12 Oxalis purpurea 18 Zephyranthes drummondii 12 Lachenalia mutabilis 17 Zephyranthes reginae 11 Moraea sp. 17 Amaryllis belladonna 10 Amaryllis belladonna 14 Calochortus venustus 10 Oxalis luteola 14 Zephyranthes fosteri 10 Albuca sp. 13 Calochortus luteus 9 Moraea villosa 13 Crinum bulbispermum 9 Oxalis caprina 13 Habranthus robustus 9 Oxalis imbricata 12 Haemanthus albiflos 9 Oxalis namaquana 12 Nerine bowdenii 9 Oxalis engleriana 11 Cyclamen graecum 8 Oxalis melanosticta 'Ken Aslet'11 Fritillaria affinis 8 Moraea ciliata 10 Habranthus brachyandrus 8 Oxalis commutata 10 Zephyranthes 'Pink Beauty' 8 Summary of offerings in the PBS Bulb Exchange, Dec 2012- Nov 2019 Most taxa specify to species level. 34 taxa were listed as Genus sp. for bulbs 23 taxa were listed as Genus sp. for seeds 141 taxa were listed with quoted 'Variety' Top 20 Most often listed Genera BULBS SEEDS Genus N items BXs Genus N items BXs Oxalis 450 64 Zephyranthes 202 35 Lachenalia 125 47 Calochortus 94 15 Moraea 99 31 Moraea -
News from the CREW
Volume 6 • March 200 News from the CREW lthough 2009 has been a Asteraceae family) in full flower. REW, the Custodians of Areally challenging year with These plants are usually rather C Rare and Endangered the global recession having had inconspicuous and are very hard Wildflowers, is a programme a heavy impact on all of us, it to spot when not flowering, so that involves volunteers from we were very lucky to catch it could not break the strong spir- the public in the monitoring it of CREW. Amidst the great in flower. The CREW team has taken a special interest in the and conservation of South challenges we came up tops genus Marasmodes (we even Africa’s threatened plants. once again, with some excep- have a day in April dedicated to CREW aims to capacitate a tionally great discoveries. the monitoring of this genus) network of volunteers from as they all occur in the lowlands a range of socio-economic Our first great adventure for and are severely threatened. I backgrounds to monitor the year took place in the knew from the herbarium speci- and conserve South Afri- Villiersdorp area. We had to mens that there have not been ca’s threatened plant spe- collect flowering material of any collections of Marasmodes Prismatocarpus lycioides, a data cies. The programme links from the Villiersdorp area and volunteers with their local deficient species in the Campan- was therefore very excited conservation agencies and ulaceae family. We rediscovered about this discovery. As usual, this species in the area in 2008 my first reaction was: ‘It’s a particularly with local land and all we had to go on was a new species!’ but I soon so- stewardship initiatives to en- scrappy nonflowering branch. -
Boophone Disticha
Micropropagation and pharmacological evaluation of Boophone disticha Lee Cheesman Submitted in fulfilment of the academic requirements for the degree of Doctor of Philosophy Research Centre for Plant Growth and Development School of Life Sciences University of KwaZulu-Natal, Pietermaritzburg April 2013 COLLEGE OF AGRICULTURE, ENGINEERING AND SCIENCES DECLARATION 1 – PLAGIARISM I, LEE CHEESMAN Student Number: 203502173 declare that: 1. The research contained in this thesis, except where otherwise indicated, is my original research. 2. This thesis has not been submitted for any degree or examination at any other University. 3. This thesis does not contain other persons’ data, pictures, graphs or other information, unless specifically acknowledged as being sourced from other persons. 4. This thesis does not contain other persons’ writing, unless specifically acknowledged as being sourced from other researchers. Where other written sources have been quoted, then: a. Their words have been re-written but the general information attributed to them has been referenced. b. Where their exact words have been used, then their writing has been placed in italics and inside quotation marks, and referenced. 5. This thesis does not contain text, graphics or tables copied and pasted from the internet, unless specifically acknowledged, and the source being detailed in the thesis and in the reference section. Signed at………………………………....on the.....….. day of ……......……….2013 ______________________________ SIGNATURE i STUDENT DECLARATION Micropropagation and pharmacological evaluation of Boophone disticha I, LEE CHEESMAN Student Number: 203502173 declare that: 1. The research reported in this dissertation, except where otherwise indicated is the result of my own endeavours in the Research Centre for Plant Growth and Development, School of Life Sciences, University of KwaZulu-Natal, Pietermaritzburg. -
Clivia Miniata Colour Mutations and Their Breeding
Clivia Miniata Colour Mutations and their Breeding I don’t profess to be geneticists or to know very much about the way in which colour is inherited in Clivia, but by taking a very simple approach of line breeding and a lot of trial and error I have managed to produce true breeding lines of Clivia. This knowledge will be valuable to any breeder wishing to perpetuate a particular colour mutation. In the best interest of Clivia I have decided to write this article and attempt to share what I have learnt with others. It is my opinion that for a particular colour mutation to be inherited by sexual reproduction, a pathway has to occur i.e. the genes or other factors influencing the colour would have to line up. A simple way in which to view the chromosomes and the loci on which these chromosomes have mutated is by taking two rulers and placing them side by side, each representing different plants with similar colour mutations and only if both plants have mutated on the same point of the chromosomes (rulers) would the mutation be transferred to the off spring by sexual reproduction. Plants are relatively easy to line breed / inbreed because of the fact that they can be self- pollinated. Unfortunately, mechanisms are in place in plants that inhibit self-pollination and so more effort is required to perpetuate these colour mutations. The best-known colour mutation in Clivia is the yellow mutation occurring in Clivia miniata. Even here just because two plants are yellow doesn’t necessarily mean they have mutated at the same loci on the chromosome. -
Scanning Electron Microscopy of the Leaf Epicuticular Waxes of the Genus Gethyllis L
Soulh Afnc.1n Journal 01 Bol811Y 2001 67 333-343 Copynghl €I NISC Ply LId Pnmed In South Alnca - All ngills leserved SOUTH AFRICAN JOURNAL OF BOTANY ISSN 0254- 5299 Scanning electron microscopy of the leaf epicuticular waxes of the genus Gethyllis L. (Amaryllidaceae) and prospects for a further subdivision C Weiglin Technische Universitat Berlin, Herbarium BTU, Sekr. FR I- I, Franklinstrasse 28-29, 0-10587 Berlin, Germany e-mail: [email protected] Recei ved 23 August 2000, accepled in revised form 19 January 2001 The leaf epicuticular wax ultrastructure of 32 species of ridged rodlets is conspicuous and is interpreted as the genus Gethyllis are for the first time investigated being convergent. In three species wax dimorphism was and discussed. Non-entire platelets were observed in discovered, six species show a somewhat rosette-like 12 species, entire platelets with transitions to granules orientation of non-entire or entire platelets and in four in seven species, membranous platelets in nine species a tendency to parallel orientation of non-entire species and smooth layers in eight species, Only or entire platelets was evident. It seems that Gethyllis, GethyJlis transkarooica is distinguished by its trans from its wax morphology, is highly diverse and versely ridged rodlets. The occurrence of transversely deserves further subdivision. Introduction The outer epidermal cell walls of nearly all land plants are gle species among larger taxa, cu ltivated plants , varieties covered by a cuticle cons isting mainly of cutin, an insoluble and mutants (Juniper 1960, Leigh and Matthews 1963, Hall lipid pOlyester of substituted aliphatic acids and long chain et al. -
The Green Scene Brighten Winter with a Clivia Plant
Marion County Extension 210 N. Iowa St. Knoxville, IA 50138 641.842.2014 [email protected] February, 2019 Volume 17, Issue 2 The Green Scene Save a tree! Send your email address to [email protected] to receive this publication via e-mail. Brighten Winter with a Clivia Plant By Richard Jauon Flowers are one of the best antidotes to the icy winds of winter, and growing a houseplant that buds and blooms inside while all is dormant outside is particularly satisfying. This winter, as an alternative to the brightly blooming azaleas, chrysanthemums or traditional holiday plants, consider growing a clivia plant. What is a clivia? Clivia or kaffir lily (Clivia spp.) is a herbaceous flowering plant native to South Africa. Plants have long, arching, strap-like leaves (similar to an amaryllis) and produce dense clusters of trumpet-shaped flowers atop 18 to 24 inch stems. The flowers of Clivia minia- ta are typically orange with yellow eyes or centers. However, there are also several rare and expensive yellow-flowering cultivars. While clivias are not winter hardy in Iowa, they are excellent, low maintenance houseplants. How do I get a clivia to bloom? Clivias need a rest period of six to 12 weeks in fall and winter to initiate flower bud development. Temperatures dur- ing this time should be 40 to 55 degrees Fahrenheit. A guest bedroom, porch or a partially heated garage (temperatures must remain above 35 F) may be suitable plant locations. Water sparingly (about once a month). When flower stalks appear, move plants to a slightly warmer location and begin to water more frequently. -
Plant Life MagillS Encyclopedia of Science
MAGILLS ENCYCLOPEDIA OF SCIENCE PLANT LIFE MAGILLS ENCYCLOPEDIA OF SCIENCE PLANT LIFE Volume 4 Sustainable Forestry–Zygomycetes Indexes Editor Bryan D. Ness, Ph.D. Pacific Union College, Department of Biology Project Editor Christina J. Moose Salem Press, Inc. Pasadena, California Hackensack, New Jersey Editor in Chief: Dawn P. Dawson Managing Editor: Christina J. Moose Photograph Editor: Philip Bader Manuscript Editor: Elizabeth Ferry Slocum Production Editor: Joyce I. Buchea Assistant Editor: Andrea E. Miller Page Design and Graphics: James Hutson Research Supervisor: Jeffry Jensen Layout: William Zimmerman Acquisitions Editor: Mark Rehn Illustrator: Kimberly L. Dawson Kurnizki Copyright © 2003, by Salem Press, Inc. All rights in this book are reserved. No part of this work may be used or reproduced in any manner what- soever or transmitted in any form or by any means, electronic or mechanical, including photocopy,recording, or any information storage and retrieval system, without written permission from the copyright owner except in the case of brief quotations embodied in critical articles and reviews. For information address the publisher, Salem Press, Inc., P.O. Box 50062, Pasadena, California 91115. Some of the updated and revised essays in this work originally appeared in Magill’s Survey of Science: Life Science (1991), Magill’s Survey of Science: Life Science, Supplement (1998), Natural Resources (1998), Encyclopedia of Genetics (1999), Encyclopedia of Environmental Issues (2000), World Geography (2001), and Earth Science (2001). ∞ The paper used in these volumes conforms to the American National Standard for Permanence of Paper for Printed Library Materials, Z39.48-1992 (R1997). Library of Congress Cataloging-in-Publication Data Magill’s encyclopedia of science : plant life / edited by Bryan D. -
Mechanical Properties of Plant Underground Storage Organs and Implications for Dietary Models of Early Hominins Nathaniel J
Marshall University Marshall Digital Scholar Biological Sciences Faculty Research Biological Sciences Summer 7-26-2008 Mechanical Properties of Plant Underground Storage Organs and Implications for Dietary Models of Early Hominins Nathaniel J. Dominy Erin R. Vogel Justin D. Yeakel Paul J. Constantino Biological Sciences, [email protected] Peter W. Lucas Follow this and additional works at: http://mds.marshall.edu/bio_sciences_faculty Part of the Biological and Physical Anthropology Commons, and the Paleontology Commons Recommended Citation Dominy NJ, Vogel ER, Yeakel JD, Constantino P, and Lucas PW. The mechanical properties of plant underground storage organs and implications for the adaptive radiation and resource partitioning of early hominins. Evolutionary Biology 35(3): 159-175. This Article is brought to you for free and open access by the Biological Sciences at Marshall Digital Scholar. It has been accepted for inclusion in Biological Sciences Faculty Research by an authorized administrator of Marshall Digital Scholar. For more information, please contact [email protected], [email protected]. Evol Biol (2008) 35:159–175 DOI 10.1007/s11692-008-9026-7 RESEARCH ARTICLE Mechanical Properties of Plant Underground Storage Organs and Implications for Dietary Models of Early Hominins Nathaniel J. Dominy Æ Erin R. Vogel Æ Justin D. Yeakel Æ Paul Constantino Æ Peter W. Lucas Received: 16 April 2008 / Accepted: 15 May 2008 / Published online: 26 July 2008 Ó Springer Science+Business Media, LLC 2008 Abstract The diet of early human ancestors has received 98 plant species from across sub-Saharan Africa. We found renewed theoretical interest since the discovery of elevated that rhizomes were the most resistant to deformation and d13C values in the enamel of Australopithecus africanus fracture, followed by tubers, corms, and bulbs. -
(Tribe Haemantheae) Inferred from Plastid and Nuclear Non-Coding DNA Sequences
Plant Syst. Evol. 244: 141–155 (2004) DOI 10.1007/s00606-003-0085-z Generic relationships among the baccate-fruited Amaryllidaceae (tribe Haemantheae) inferred from plastid and nuclear non-coding DNA sequences A. W. Meerow1, 2 and J. R. Clayton1 1 USDA-ARS-SHRS, National Germplasm Repository, Miami, Florida, USA 2 Fairchild Tropical Garden, Miami, Florida, USA Received October 22, 2002; accepted September 3, 2003 Published online: February 12, 2004 Ó Springer-Verlag 2004 Abstract. Using sequences from the plastid trnL-F Key words: Amaryllidaceae, Haemantheae, geo- region and nrDNA ITS, we investigated the phy- phytes, South Africa, monocotyledons, DNA, logeny of the fleshy-fruited African tribe Haeman- phylogenetics, systematics. theae of the Amaryllidaceae across 19 species representing all genera of the tribe. ITS and a Baccate fruits have evolved only once in the combined matrix produce the most resolute and Amaryllidaceae (Meerow et al. 1999), and well-supported tree with parsimony analysis. Two solely in Africa, but the genera possessing main clades are resolved, one comprising the them have not always been recognized as a monophyletic rhizomatous genera Clivia and Cryp- monophyletic group. Haemanthus L. and tostephanus, and a larger clade that unites Haemanthus and Scadoxus as sister genera to an Gethyllis L. were the first two genera of the Apodolirion/Gethyllis subclade. One of four group to be described (Linneaus 1753). Her- included Gethyllis species, G. lanuginosa, resolves bert (1837) placed Haemanthus (including as sister to Apodolirion with ITS. Relationships Scadoxus Raf.) and Clivia Lindl. in the tribe among the Clivia species are not in agreement with Amaryllidiformes, while Gethyllis was classi- a previous published phylogeny. -
Listado De Todas Las Plantas Que Tengo Fotografiadas Ordenado Por Familias Según El Sistema APG III (Última Actualización: 2 De Septiembre De 2021)
Listado de todas las plantas que tengo fotografiadas ordenado por familias según el sistema APG III (última actualización: 2 de Septiembre de 2021) GÉNERO Y ESPECIE FAMILIA SUBFAMILIA GÉNERO Y ESPECIE FAMILIA SUBFAMILIA Acanthus hungaricus Acanthaceae Acanthoideae Metarungia longistrobus Acanthaceae Acanthoideae Acanthus mollis Acanthaceae Acanthoideae Odontonema callistachyum Acanthaceae Acanthoideae Acanthus spinosus Acanthaceae Acanthoideae Odontonema cuspidatum Acanthaceae Acanthoideae Aphelandra flava Acanthaceae Acanthoideae Odontonema tubaeforme Acanthaceae Acanthoideae Aphelandra sinclairiana Acanthaceae Acanthoideae Pachystachys lutea Acanthaceae Acanthoideae Aphelandra squarrosa Acanthaceae Acanthoideae Pachystachys spicata Acanthaceae Acanthoideae Asystasia gangetica Acanthaceae Acanthoideae Peristrophe speciosa Acanthaceae Acanthoideae Barleria cristata Acanthaceae Acanthoideae Phaulopsis pulchella Acanthaceae Acanthoideae Barleria obtusa Acanthaceae Acanthoideae Pseuderanthemum carruthersii ‘Rubrum’ Acanthaceae Acanthoideae Barleria repens Acanthaceae Acanthoideae Pseuderanthemum carruthersii var. atropurpureum Acanthaceae Acanthoideae Brillantaisia lamium Acanthaceae Acanthoideae Pseuderanthemum carruthersii var. reticulatum Acanthaceae Acanthoideae Brillantaisia owariensis Acanthaceae Acanthoideae Pseuderanthemum laxiflorum Acanthaceae Acanthoideae Brillantaisia ulugurica Acanthaceae Acanthoideae Pseuderanthemum laxiflorum ‘Purple Dazzler’ Acanthaceae Acanthoideae Crossandra infundibuliformis Acanthaceae Acanthoideae Ruellia -
Newsletter No. 4 Autumn 2005
The Southern African Bulb Group Newsletter No. 4 Autumn 2005 The Southern African Bulb Group was initiated by a group of enthusiasts on April 4th 2004. The objective of the group is to further the understanding of the cultivation of Southern African bulbs, where `bulbs' is used in the broad sense to encompass bulb-, corm- and tuber- possessing Southern African plants, including `dicots' such as Oxalis. In the first instance the group will be run on an informal basis, with an initial subscription of £5 invited from participants. Committee: Robin Attrill (Membership secretary and Newsletter editor), Margaret Corina (Treasurer), Stefan Rau and Terry Smale Editorial This issue of the newsletter contains a report of the meeting of the group held at Rupert Bowlby's Nursery on April 9th 2005, an article on Crinum moorei by David Corina, information on recent literature of interest to growers of Southern African bulbs, and an updated list of suppliers of seed and bulbs/corms of Southern African geophytes. In addition a balance sheet covering the first year of operation of the group is attached. With respect to the supplier list, please let me know if you are aware of other sources which should be included. As I have previously stated the group welcomes articles, and suggestions, for inclusion in future newsletters. Contributions (hand/typewritten and electronic are acceptable!) are urgently required and should be sent to the newsletter editor at 17 Waterhouse Moor, Harlow, Essex, CM18 6BA (Email [email protected] ) Publication of the next issue is scheduled for December 2005. Report on visit to Rupert Bowlby - Saturday 9 th April 2005 by David Corina About 20 members attended the event, and the Group would like to thank Rupert for his hospitality at the event and for opening his collection to the public gaze. -
Vegetation Survey of Mount Gorongosa
VEGETATION SURVEY OF MOUNT GORONGOSA Tom Müller, Anthony Mapaura, Bart Wursten, Christopher Chapano, Petra Ballings & Robin Wild 2008 (published 2012) Occasional Publications in Biodiversity No. 23 VEGETATION SURVEY OF MOUNT GORONGOSA Tom Müller, Anthony Mapaura, Bart Wursten, Christopher Chapano, Petra Ballings & Robin Wild 2008 (published 2012) Occasional Publications in Biodiversity No. 23 Biodiversity Foundation for Africa P.O. Box FM730, Famona, Bulawayo, Zimbabwe Vegetation Survey of Mt Gorongosa, page 2 SUMMARY Mount Gorongosa is a large inselberg almost 700 sq. km in extent in central Mozambique. With a vertical relief of between 900 and 1400 m above the surrounding plain, the highest point is at 1863 m. The mountain consists of a Lower Zone (mainly below 1100 m altitude) containing settlements and over which the natural vegetation cover has been strongly modified by people, and an Upper Zone in which much of the natural vegetation is still well preserved. Both zones are very important to the hydrology of surrounding areas. Immediately adjacent to the mountain lies Gorongosa National Park, one of Mozambique's main conservation areas. A key issue in recent years has been whether and how to incorporate the upper parts of Mount Gorongosa above 700 m altitude into the existing National Park, which is primarily lowland. [These areas were eventually incorporated into the National Park in 2010.] In recent years the unique biodiversity and scenic beauty of Mount Gorongosa have come under severe threat from the destruction of natural vegetation. This is particularly acute as regards moist evergreen forest, the loss of which has accelerated to alarming proportions.