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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 -
The Effect of Cultivation and Plant Age on the Pharmacological Activity of Merwilla Natalensis Bulbs
South African Journal of Botany 2005, 71(2): 191–196 Copyright © NISC Pty Ltd Printed in South Africa — All rights reserved SOUTH AFRICAN JOURNAL OF BOTANY ISSN 1727–9321 The effect of cultivation and plant age on the pharmacological activity of Merwilla natalensis bulbs SG Sparg, AK Jäger and J van Staden* Research Centre for Plant Growth and Development, University of KwaZulu-Natal Pietermaritzburg, Private Bag X01, Scottsville 3209, South Africa * Corresponding author, e-mail: [email protected] Received 5 March 2004, accepted in revised form 27 August 2004 Merwilla natalensis bulbs were cultivated at two thesis by COX-1, with activity decreasing as the bulbs different sites under different treatments. Bulbs were matured. The cultivation treatments had a significant harvested every six months for a period of two years effect on the antihelmintic activity of bulbs cultivated at and were tested for antibacterial, anti-inflammatory and the Fort Hare site. Results suggest that irrigation might anthelmintic activity. The cultivation treatments had no increase the antihelmintic activity of the bulbs if culti- significant effect (P ≤ 0.05) on neither the antibacterial vated in areas of low rainfall. The age of the bulbs at activity, nor the anti-inflammatory activity. However, the both sites had a significant effect on the antihelmintic age of the bulbs had a significant effect against the test activity, with activity increasing with plant maturity. bacteria and on the inhibition of prostaglandin syn- Introduction Merwilla natalensis (Planchon) Speta (synonym Scilla varied when the plants were grown in different geographical natalensis) is ranked as one of the more commonly-sold regions. -
Spotting Plants' Microfilament Morphologies and Nanostructures
Spotting plants’ microfilament morphologies and nanostructures a a b b a,c b,d,1 Ana P. Almeida , João Canejo , Urban Mur , Simon Copar , Pedro L. Almeida , Slobodan Žumer , and Maria Helena Godinhoa,1 aCentro de Investigação em Materiais/Institute for Nanomodelling, Nanostructures and Nanofabrication, Departamento de Ciência dos Materiais, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516 Caparica, Portugal; bFaculty of Mathematics and Physics, University of Ljubljana, 1000 Ljubljana, Slovenia; cÁrea Departamental de Física, Instituto Superior de Engenharia de Lisboa, Instituto Politécnico de Lisboa, 1959-007 Lisboa, Portugal; and dCondensed Matter Physics, Jozef Stefan Institute, 1000 Ljubljana, Slovenia Edited by David A. Weitz, Harvard University, Cambridge, MA, and approved May 21, 2019 (received for review January 20, 2019) The tracheary system of plant leaves is composed of a cellulose droplets (18). Quantitative measurements were also performed skeleton with diverse hierarchical structures. It is built of polygo- with microfilaments that promote planar or helicoidal alignment, nally bent helical microfilaments of cellulose-based nanostructures inserted in cells with well-defined homeotropic anchoring at the coated by different layers, which provide them high compression surfaces. Manipulation of the nematic texture with electric and resistance, elasticity, and roughness. Their function includes the magnetic fields was used to determine the microfilament’s chi- transport of water and nutrients from the roots to the leaves. rality and handedness (18, 19). The correspondence between the Unveiling details about local interactions of tracheary elements with nematic liquid crystal anchoring properties of natural microfila- surrounding material, which varies between plants due to adaptation ments and their surface morphology and chemical makeup is a to different environments, is crucial for understanding ascending fluid challenging open question, as discussed previously in literature (20). -
Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese -
SOUTHERN CALIFORNIA HORTICULTURAL SOCIETY Where Passionate Gardeners Meet to Share Knowledge and Learn from Each Other
SOUTHERN CALIFORNIA HORTICULTURAL SOCIETY Where passionate gardeners meet to share knowledge and learn from each other. socalhort.org June 2013 Newsletter OUR NEXT MEETING PLANT FORUM NEXT SHARING SECRETS Bring one or more plants, QUESTION Thursday, June 13 flowers, seeds or fruits for IN THIS ISSUE Inspired by this month’s 7:30 pm display and discussion at the program, the Sharing Secrets May Meeting Recap Friendship Auditorium Plant Forum. We will soon have question for June is: by Steven Gerischer ............... 2 3201 Riverside Drive an improved, downloadable Sharing Secrets ......................... 2 Los Angeles CA 90027 PDF version of the plant "Do you preserve any of the information card. Anyone produce you grow, and Coffee in the Garden................2 We meet the second Thursday bringing in material for the how?” Upcoming Field Trips & Coffee In of each month at 7:30 pm Plant Forum table should ______________________________ The Garden ............................... 2 remember to pick up an You can answer on the cards March 2013 Green Sheet by This meeting is free to SCHS exhibitor’s ticket for the Plant we’ll supply at our June 13 James E. Henrich............3, 4 & 5 members and is $5 for non- Raffle, on nights when a raffle meeting, on our MemberLodge members without a guest pass. is conducted. These plants are website or e-mail your Horticultural Happenings also included in our response to by Bettina Gatti ........................6 newsletter’s Green Sheet. [email protected] by Friday, Upcoming 2013 SCHS June 14. Programs ................................... 7 The June Meeting In the 21st century we take food PLANT RAFFLE RETURNS! preservation for granted. -
1 the Global Flower Bulb Industry
1 The Global Flower Bulb Industry: Production, Utilization, Research Maarten Benschop Hobaho Testcentrum Hillegom, The Netherlands Rina Kamenetsky Department of Ornamental Horticulture Agricultural Research Organization The Volcani Center Bet Dagan 50250, Israel Marcel Le Nard Institut National de la Recherche Agronomique 29260 Ploudaniel, France Hiroshi Okubo Laboratory of Horticultural Science Kyushu University 6-10-1 Hakozaki, Higashi-ku Fukuoka 812-8581, Japan August De Hertogh Department of Horticultural Science North Carolina State University Raleigh, NC 29565-7609, USA COPYRIGHTED MATERIAL I. INTRODUCTION II. HISTORICAL PERSPECTIVES III. GLOBALIZATION OF THE WORLD FLOWER BULB INDUSTRY A. Utilization and Development of Expanded Markets Horticultural Reviews, Volume 36 Edited by Jules Janick Copyright Ó 2010 Wiley-Blackwell. 1 2 M. BENSCHOP, R. KAMENETSKY, M. LE NARD, H. OKUBO, AND A. DE HERTOGH B. Introduction of New Crops C. International Conventions IV. MAJOR AREAS OF RESEARCH A. Plant Breeding and Genetics 1. Breeders’ Right and Variety Registration 2. Hortus Bulborum: A Germplasm Repository 3. Gladiolus 4. Hyacinthus 5. Iris (Bulbous) 6. Lilium 7. Narcissus 8. Tulipa 9. Other Genera B. Physiology 1. Bulb Production 2. Bulb Forcing and the Flowering Process 3. Morpho- and Physiological Aspects of Florogenesis 4. Molecular Aspects of Florogenesis C. Pests, Physiological Disorders, and Plant Growth Regulators 1. General Aspects for Best Management Practices 2. Diseases of Ornamental Geophytes 3. Insects of Ornamental Geophytes 4. Physiological Disorders of Ornamental Geophytes 5. Exogenous Plant Growth Regulators (PGR) D. Other Research Areas 1. Specialized Facilities and Equipment for Flower Bulbs52 2. Transportation of Flower Bulbs 3. Forcing and Greenhouse Technology V. MAJOR FLOWER BULB ORGANIZATIONS A. -
Dyuhei Sato Division of Genetics, Bot. Inst. Faculty of Science, Tokyo
ANALYSIS OF THE KARYOTYPES IN YUCCA, A GA VE AND THE RELATED GENERA WITH SPECIAL REFERENCE TO THE PHYLOGENETIC SIGNIFICANCEI~ Dyuhei SATo Divisionof Genetics, Bot. Inst. Faculty of Science, Tokyo Imperial University McKelvey and Sax (2933) have called attention to the existence of taxonomic and cytological similarities of the genera Yucca, Hesperoyucca, Gleistvucca,Hesperoaloe and Samuela of the Liliaceae with the genera Agave and Fourcroya which belong to a related family, Amaryllidaceae. Wh.itaker (1934) also has reported that Polianhes and Fourcroya have exactly the same chromosome constitution as the Yucca-Abave karyotype (5 long and 25 short chromosomes) (Figs. 1, 2). These observations when considered in respect to taxonomic resemblances, seem to indicate that the genera mentioned above are more closely related than it is shown by their classifica- tion into distinct families. Whitaker also has remarked that Dasylirion (2n=38) and ATolina(2n=36) in Yucceae and Doryanthes (2n=36) in Agavoideae are of different karyotypes from the Yucca-Agave type. In the present work an analysis of the karyotypes in Liliaceous plants has been attempted and several karyotypes have been found in Scilloideae. Eucornis and Carassia have been selected with the purpose of discovering a possible connecting link between these genera and the Yucca-Agave group. In the present paper an analysis of the karyotypes of the following species is given. LILIACEAE Scilloideae 211 Fig. Euconis undulata 60=8L+8M+44S (4b)2) 3 Euconsispallidi ora 60=8L+8M+44S (4b) 4 Eucomispunctata 60=8L±8M+44S (4b) 5 Camassiaescrema 30=6L+24S (2b) 6 Yucceae Yuccafilamentosa 30 60=1OL+50S (2b) 1, 7 Yuccarecurvifolia 30 60=1OL+50S (2b) 2, 8 Yuccaaloifolia 60=1OL+50S (2b) 9 „ var. -
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Bothalia 25,2: 255-264 (1995) OBITUARIES WINSOME (BUDDY) BARKER (1907-1994) The death of Winsome Barker (Figure 1) on 27 De ment. Field work was not neglected either. Yet again the cember 1994 at Wynberg, Cape, was more than just the potent influence of Louisa Bolus made itself felt. Here close of a long chapter in the history of Kirstenbosch. It Buddy describes her first serious collecting expedition: was—particularly for the Compton Herbarium—the end ‘It was Mrs Bolus who took me on my first botanical of an era. From 1929 when she arrived at Kirstenbosch collecting trip to the North Western Cape, where at Nieu- to take up the Solly Scholarship until the late 1980’s, when woudtville in an exceptionally good season, I saw my first increasing infirmity prevented her from visiting the her spring display in all its glory, an unforgettable memory, barium, her entire life revolved around the collection she which will remain with me always, as being more won built up with such devotion and diligence. Sadly, so many derful than my wildest dreams could have imagined. The years have passed since her retirement in 1972 that now wealth of species, as well as their beauty astounded me, there are few members of the present staff of the National and my ambition to be a systematic botanist began to crys- Botanical Institute who still remember her or are even talise.’ aware of the magnitude of the contribution she made over a period of 43 years. In short, the story of her life and At the conclusion of her scholarship term Buddy was work is essentially the history of the founding and early contracted to work in the herbarium at Kew by the Ben- development of the Compton Herbarium at Kirstenbosch. -
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 -
Insights from Microsporogenesis in Asparagales
EVOLUTION & DEVELOPMENT 9:5, 460–471 (2007) Constraints and selection: insights from microsporogenesis in Asparagales Laurent Penet,a,1,Ã Michel Laurin,b Pierre-Henri Gouyon,a,c and Sophie Nadota aLaboratoire Ecologie, Syste´matique et Evolution, Batiment 360, Universite´ Paris-Sud, 91405 Orsay Ce´dex, France bUMR CNRS 7179, Universite´ Paris 6FPierre & Marie Curie, 2 place Jussieu, Case 7077, 75005 Paris, France cMuse´um National d’Histoire Naturelle, De´partement de Syste´matique et Evolution Botanique, 12 rue Buffon, 75005 Paris CP 39, France ÃAuthor for correspondence (email: [email protected]) 1Current address: Department of Biological Sciences, University of Pittsburgh, 4249 Fifth & Ruskin, Pittsburgh, PA 15260, USA. SUMMARY Developmental constraints have been proposed different characteristics of microsporogenesis, only cell to interfere with natural selection in limiting the available wall formation appeared as constrained. We show that set of potential adaptations. Whereas this concept has constraints may also result from biases in the correlated long been debated on theoretical grounds, it has been occurrence of developmental steps (e.g., lack of successive investigated empirically only in a few studies. In this article, cytokinesis when wall formation is centripetal). We document we evaluate the importance of developmental constraints such biases and their potential outcomes, notably the during microsporogenesis (male meiosis in plants), with an establishment of intermediate stages, which allow emphasis on phylogenetic patterns in Asparagales. Different development to bypass such constraints. These insights are developmental constraints were tested by character discussed with regard to potential selection on pollen reshuffling or by simulated distributions. Among the morphology. INTRODUCTION 1991) also hindered tests using the concept (Pigliucci and Kaplan 2000). -
TAXON:Schizobasis Intricata SCORE:1.0 RATING:Low Risk
TAXON: Schizobasis intricata SCORE: 1.0 RATING: Low Risk Taxon: Schizobasis intricata Family: Hyacinthaceae Common Name(s): climbing onion Synonym(s): Anthericum intricatum Baker losbol Drimia intricata (Baker) J.C.Manning Schizobasis& Goldblatt dinteri K.Krause Schizobasis macowanii Baker Assessor: Chuck Chimera Status: Assessor Approved End Date: 26 Jun 2015 WRA Score: 1.0 Designation: L Rating: Low Risk Keywords: Geophyte, Bulb-forming, Self-fertile, Seed Producing, Atelechorous Qsn # Question Answer Option Answer 101 Is the species highly domesticated? y=-3, n=0 n 102 Has the species become naturalized where grown? 103 Does the species have weedy races? Species suited to tropical or subtropical climate(s) - If 201 island is primarily wet habitat, then substitute "wet (0-low; 1-intermediate; 2-high) (See Appendix 2) High tropical" for "tropical or subtropical" 202 Quality of climate match data (0-low; 1-intermediate; 2-high) (See Appendix 2) High 203 Broad climate suitability (environmental versatility) Native or naturalized in regions with tropical or 204 y=1, n=0 y subtropical climates Does the species have a history of repeated introductions 205 y=-2, ?=-1, n=0 ? outside its natural range? 301 Naturalized beyond native range y = 1*multiplier (see Appendix 2), n= question 205 n 302 Garden/amenity/disturbance weed n=0, y = 1*multiplier (see Appendix 2) n 303 Agricultural/forestry/horticultural weed n=0, y = 2*multiplier (see Appendix 2) n 304 Environmental weed n=0, y = 2*multiplier (see Appendix 2) n 305 Congeneric weed n=0, y = -
Albuca Spiralis
Flowering Plants of Africa A magazine containing colour plates with descriptions of flowering plants of Africa and neighbouring islands Edited by G. Germishuizen with assistance of E. du Plessis and G.S. Condy Volume 62 Pretoria 2011 Editorial Board A. Nicholas University of KwaZulu-Natal, Durban, RSA D.A. Snijman South African National Biodiversity Institute, Cape Town, RSA Referees and other co-workers on this volume H.J. Beentje, Royal Botanic Gardens, Kew, UK D. Bridson, Royal Botanic Gardens, Kew, UK P. Burgoyne, South African National Biodiversity Institute, Pretoria, RSA J.E. Burrows, Buffelskloof Nature Reserve & Herbarium, Lydenburg, RSA C.L. Craib, Bryanston, RSA G.D. Duncan, South African National Biodiversity Institute, Cape Town, RSA E. Figueiredo, Department of Plant Science, University of Pretoria, Pretoria, RSA H.F. Glen, South African National Biodiversity Institute, Durban, RSA P. Goldblatt, Missouri Botanical Garden, St Louis, Missouri, USA G. Goodman-Cron, School of Animal, Plant and Environmental Sciences, University of the Witwatersrand, Johannesburg, RSA D.J. Goyder, Royal Botanic Gardens, Kew, UK A. Grobler, South African National Biodiversity Institute, Pretoria, RSA R.R. Klopper, South African National Biodiversity Institute, Pretoria, RSA J. Lavranos, Loulé, Portugal S. Liede-Schumann, Department of Plant Systematics, University of Bayreuth, Bayreuth, Germany J.C. Manning, South African National Biodiversity Institute, Cape Town, RSA A. Nicholas, University of KwaZulu-Natal, Durban, RSA R.B. Nordenstam, Swedish Museum of Natural History, Stockholm, Sweden B.D. Schrire, Royal Botanic Gardens, Kew, UK P. Silveira, University of Aveiro, Aveiro, Portugal H. Steyn, South African National Biodiversity Institute, Pretoria, RSA P. Tilney, University of Johannesburg, Johannesburg, RSA E.J.