Calla History and Culture
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Liliaceae S.L. (Lily Family)
Liliaceae s.l. (Lily family) Photo: Ben Legler Photo: Hannah Marx Photo: Hannah Marx Lilium columbianum Xerophyllum tenax Trillium ovatum Liliaceae s.l. (Lily family) Photo: Yaowu Yuan Fritillaria lanceolata Ref.1 Textbook DVD KRR&DLN Erythronium americanum Allium vineale Liliaceae s.l. (Lily family) Herbs; Ref.2 Stems often modified as underground rhizomes, corms, or bulbs; Flowers actinomorphic; 3 sepals and 3 petals or 6 tepals, 6 stamens, 3 carpels, ovary superior (or inferior). Tulipa gesneriana Liliaceae s.l. (Lily family) “Liliaceae” s.l. (sensu lato: “in the broad sense”) - Lily family; 288 genera/4950 species, including Lilium, Allium, Trillium, Tulipa; This family is treated in a very broad sense in this class, as in the Flora of the Pacific Northwest. The “Liliaceae” s.l. taught in this class is not monophyletic. It is apparent now that the family should be treated in a narrower sense and some of the members should form their own families. Judd et al. recognize 15+ families: Agavaceae, Alliaceae, Amarylidaceae, Asparagaceae, Asphodelaceae, Colchicaceae, Dracaenaceae (Nolinaceae), Hyacinthaceae, Liliaceae, Melanthiaceae, Ruscaceae, Smilacaceae, Themidaceae, Trilliaceae, Uvulariaceae and more!!! (see web reading “Consider the Lilies”) Iridaceae (Iris family) Photo: Hannah Marx Photo: Hannah Marx Iris pseudacorus Iridaceae (Iris family) Photo: Yaowu Yuan Photo: Yaowu Yuan Sisyrinchium douglasii Sisyrinchium sp. Iridaceae (Iris family) Iridaceae - 78 genera/1750 species, Including Iris, Gladiolus, Sisyrinchium. Herbs, aquatic or terrestrial; Underground stems as rhizomes, bulbs, or corms; Leaves alternate, 2-ranked and equitant Ref.3 (oriented edgewise to the stem; Gladiolus italicus Flowers actinomorphic or zygomorphic; 3 sepals and 3 petals or 6 tepals; Stamens 3; Ovary of 3 fused carpels, inferior. -
Arum Lily Control
ARUM LILY CONTROL Nature Conservation Information Sheet Why control arum lilies? Arum lily (Zantedeschia aethiopica) is native to South Africa and was introduced to Australia as an ornamental garden plant. It has become a serious weed in the south west of Western Australia in both pasture and bushland, particularly in damp areas but also invading drier sites. Arum lily is spread by birds and invades areas of good quality native vegetation. Often forming dense monocultures it out competes native understorey species reducing biodiversity and decreasing habitat and food resources for native animals. Arum lily is poisonous to most stock, pets and humans. Symptoms can include swelling of the lips, tongue, and throat, stomach pain, vomiting and severe diarrhoea. Ingestion of the plant may be fatal. The toxicity is due to sequestering of calcium oxalate crystals and possibly other toxic compounds by the plant. Arum lily is a listed as a Declared Plant under the Biosecurity and Agriculture Management Act 2007. Understanding the plant biology Arum lily is a perennial plant. Each year the above ground part of the plant dies back to an underground tuberous rhizome. New leaves begin to regrow in autumn and flowering generally occurs from August to December. The plant then dies back in summer. As well as reproducing via seed, arum lily reproduces vegetatively. Vegetative propagation is by small rhizomes, which are produced on the sides of the main tuber. A 2 cm tuber can produce 25-30 small rhizomes in a year. Even very small rhizomes are capable of producing new growth or new plants if they are detached or the tuber dies. -
Protecting the Natural Endangered Heritage in Romania, Croatia, Poland and Slovenia
Available online at http://journals.usamvcluj.ro/index.php/promediu ProEnvironment ProEnvironment 11 (2018) 143-157 Review The Rights of Alive – Protecting the Natural Endangered Heritage in Romania, Croatia, Poland and Slovenia CIOANCĂ Lia-Maria1*, Luminița UJICĂ2, Marijana MIKULANDRA3, Ryszard SOŁTYSIK4, Maja ČERNE5 1Babeș-Bolyai University Cluj-Napoca, University Extension Bistrița, Andrei Mureşanu st., no. 3-5, Romania 2High Scool with Sportive Program Bistrița, Calea Moldovei no. 18. Romania 3OŠ Tina Ujevi Osnovna škola Tina Ujevića Koturaška cesta 75 10000 Zagreb, Croatia 4Zespół Szkół Nr1 w Humniskach, 36 – 206, Huminska 264, Poland 5OŠ Rogaška Slatina, Kidričeva ulica 24, 3250 Rogaška Slatina Slovenia Received 23 July 2018; received and revised form 18 September 2018; accepted 25 September 2018 Available online 30 September 2018 Abstract This article deals with the impact of destructive actions of human population on natural world. As a consequence of relying on non-renewable energy sources and reckless encroachment on natural habitats a lot of plant and animal species have become extinct and more and more species are getting endangered. Thus celebrating biodiversity and solidarity for all life forms, from the tiniest one to the most complex eco-systems, has been in the centre of our attention and operational activities. Keywords: durable development, ecology, endangered species. 1. Introduction Within the massive destruction of forests and forest climate, we witness significant changes, Just as the man has passed from the stage of sometimes radical of the environment. For the animal hunter and collector up to animal raiser and farmer, and plants which have survived through a long period the natural vegetation has increasingly been subject of adaptation, a new difficult era starts again. -
Richardia Brasiliensis Gomes, 1801 CONABIO, Junio 2016 Richardia Brasiliensis Gomes, 1801
Método de Evaluación Rápida de Invasividad (MERI) para especies exóticas en México Richardia brasiliensis Gomes, 1801 CONABIO, Junio 2016 Richardia brasiliensis Gomes, 1801 Foto: Paulo Schwirkowski, 2010. Fuente: Picasaweb Richardia brasiliensis Información taxonómica Reino: Plantae División: Tracheophyta Clase: Magnoliopsida Orden: Gentianales Familia: Rubiaceae Género: Richardia Especie: Richardia brasiliensis Gomes, 1801 Nombre común: Hierba del pollo, Yerba del pato (Argentina) (SATA, 2014). Garro (Cuba), hierba de la arana (Bolivia) (CABI, 2015). Mexican clover, white-eye (PIER, 2010). Valor de invasividad: 0.4508 Categoría de riesgo: Alto 1 Método de Evaluación Rápida de Invasividad (MERI) para especies exóticas en México Richardia brasiliensis Gomes, 1801 CONABIO, Junio 2016 Descripción de la especie Planta anual perenne, herbácea, con raíz gemífera, de hasta 15-40 cm de altura. Plántula: Los cotiledones son oblongos, con una zona marrón cerca de la base. Tallos tetrágonos, pubescentes de base subleñosa, ramificados pero mas bien tendidos y radicantes que forman matas de hasta 1 m de diámetro; hojas opuestas, sésiles, elípticas u oval elípticas, de más o menos 2.5 – 5 cm de largo, agudas, enteras, atenuadas en la base, densamente pilosas en ambas caras; flores muy pequeñas; cáliz de sépalos velludos, ovado-lanceolados; corola blanca o blanco-lolacina, tubulosa, de unos 3 mm de largo, con lóbulos ovados- lanceolados, ciliados; frutos pequeños, 3-carpelares, obovado-subcilíndricos; carpelos carenados en la cara internal, tuberculados y pilosos exteriormente postrados (SATA, 2014). Distribución original Al parecer es nativa de América del Sur (PIER, 2010; Waltz et al., 2016). Crece en lugares alterados con suelos arenosos y pedregosos, así como en prados y los bordes de caminos (Waltz et al., 2016). -
Download/Empfehlung-Invasive-Arten.Pdf
09-15078 rev FORMAT FOR A PRA RECORD (version 3 of the Decision support scheme for PRA for quarantine pests) European and Mediterranean Plant Protection Organisation Organisation Européenne et Méditerranéenne pour la Protection des Plantes Guidelines on Pest Risk Analysis Lignes directrices pour l'analyse du risque phytosanitaire Decision-support scheme for quarantine pests Version N°3 PEST RISK ANALYSIS FOR LYSICHITON AMERICANUS HULTÉN & ST. JOHN (ARACEAE) Pest risk analyst: Revised by the EPPO ad hoc Panel on Invasive Alien Species Stage 1: Initiation The EWG was held on 2009-03-25/27, and was composed of the following experts: - Ms Beate Alberternst, Projektgruppe Biodiversität und Landschaftsökologie ([email protected]) - M. Serge Buholzer, Federal Department of Economic Affairs DEA ([email protected]) - M. Manuel Angel Duenas, CEH Wallingford ([email protected]) - M. Guillaume Fried, LNPV Station de Montpellier, SupAgro ([email protected]), - M. Jonathan Newman, CEH Wallingford ([email protected]), - Ms Gritta Schrader, Julius Kühn Institut (JKI) ([email protected]), - M. Ludwig Triest, Algemene Plantkunde en Natuurbeheer (APNA) ([email protected]) - M. Johan van Valkenburg, Plant Protection Service ([email protected]) 1 What is the reason for performing the Lysichiton americanus originates from the pacific coastal zone of Northwest-America PRA? and was imported into the UK at the beginning of the 20th century as a garden ornamental, and has since been sold in many European countries, including southern 1 09-15078 rev countries like Italy. It is now found in 11 European countries. The species has been observed to reduce biodiversity in the Taunus region in Germany. -
Introduction to Common Native & Invasive Freshwater Plants in Alaska
Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska Cover photographs by (top to bottom, left to right): Tara Chestnut/Hannah E. Anderson, Jamie Fenneman, Vanessa Morgan, Dana Visalli, Jamie Fenneman, Lynda K. Moore and Denny Lassuy. Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska This document is based on An Aquatic Plant Identification Manual for Washington’s Freshwater Plants, which was modified with permission from the Washington State Department of Ecology, by the Center for Lakes and Reservoirs at Portland State University for Alaska Department of Fish and Game US Fish & Wildlife Service - Coastal Program US Fish & Wildlife Service - Aquatic Invasive Species Program December 2009 TABLE OF CONTENTS TABLE OF CONTENTS Acknowledgments ............................................................................ x Introduction Overview ............................................................................. xvi How to Use This Manual .................................................... xvi Categories of Special Interest Imperiled, Rare and Uncommon Aquatic Species ..................... xx Indigenous Peoples Use of Aquatic Plants .............................. xxi Invasive Aquatic Plants Impacts ................................................................................. xxi Vectors ................................................................................. xxii Prevention Tips .................................................... xxii Early Detection and Reporting -
Size Variations of Flowering Characters in Arum Italicum (Araceae)
M. GIBERNAU,]. ALBRE, 2008 101 Size Variations of Flowering Characters in Arum italicum (Araceae) Marc Gibernau· and Jerome Albre Universite Paul Sabatier Laboratoire d'Evolution & Diversite Biologique (UMR 5174) Bat.4R3-B2 31062 Toulouse cedex 9 France *e-mail: [email protected] ABSTRACT INTRODUCTION In Arum, bigger individuals should An extreme form of flowering character proportionally invest more in the female variations according to the size is gender function (number or weight of female modification, which occurs in several flowers) than the male. The aim of this species of Arisaema (Clay, 1993). Individ paper is to quantify variations in repro ual plant gender changes from pure male, ductive characters (size of the spadix when small, to monoecious (A. dracon parts, number of inflorescences) in rela tium) or pure female (A. ringens) when tion to plant and inflorescence sizes. The large (Gusman & Gusman, 2003). This appendix represents 44% of the spadix gender change is reversible, damaged length. The female zone length represents female individuals will flower as male the 16.5% of the spadix length and is much following year (Lovett Doust & Cavers, longer than the male zone (6%). Moreover 1982). These changes are related to change these three spadix zones increase with in plant size and are explained by the plant vigour indicating an increasing size-advantage model. The size-advantage investment into reproduction and pollina model postulates a sex change when an tor attraction. It appears that the length of increase in body size is related to differen appendix increased proportionally more tial abilities to produce or sire offspring than the lengths of the fertile zones. -
Karyotype and Nucleic Acid Content in Zantedeschia Aethiopica Spr. and Zantedeschia Elliottiana Engl
African Journal of Biotechnology Vol. 11(53), pp. 11604-11609, 3 July, 2012 Available online at http://www.academicjournals.org/AJB DOI:10.5897//AJB12.061 ISSN 1684–5315 ©2012 Academic Journals Full Length Research Paper Karyotype and nucleic acid content in Zantedeschia aethiopica Spr. and Zantedeschia elliottiana Engl. Bimal Kumar Ghimire1, Chang Yeon Yu2, Ha Jung Kim3 and Ill Min Chung3* 1Department of Ethnobotany and Social Medicine, Sikkim University, Gangtok- 737 102, Sikkim, India. 2Department of Applied Plant Sciences, Kangwon National University, Chuncheon 200-701, South Korea. 3Department of Applied Life Science, Konkuk University, Seoul 143-701, South Korea. Accepted 6 June, 2012 Analysis of karyotype, nucleic deoxyribonucleic acid (DNA) content and sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) were performed in Zantedeschia aethiopica and Zantedeschia elliottiana. Mitotic metaphase in both species showed 2n=32. The chromosomes of both species were quite similar with medium length ranging from 1.55 ± 0.04 to 3.85 ± 0.12 µM in Z. aethiopica and 2.15 ± 0.04 to 3.90 ± 0.12 µM in Z. elliottiana. However, some differences were found in morphology and centromeric position among the chromosomes. Identification of individual chromosomes was carried out using chromosomes length, and centromeric positions. The karyotype of Z. aethiopica was determined to be 2n = 32 = 14 m + 18 sm and of Z. elliottiana to be 2n = 32 = 10 m + 22 sm. The 2C nuclear DNA content was found to be 3.72 ± 0.10 picograms (equivalent to 3638.16 mega base pairs) for Z. aethiopica and 1144.26 ± 0.05 picograms (equivalent to 1144.26 mega base pairs) for Z. -
Strategic Frameworks and Best Practice for Botanic Gardens
EUROGARD VII PARIS THEME A : STRATEGIC FRAMEWORKS AND BEST PRACTICE FOR BOTANIC GARDENS 01. 43 TABLE ↓OF CONTENTS CULTIVATING OUR CONNECTIONS, BUILDING SUPPORT p.43 A1 AND INFLUENCE FOR BOTANIC GARDENS LIVING COLLECTIONS: THE ESSENCE p.46 A2 OF BOTANIC GARDENS HORTICULTURE Le Projet Scientifique et Culturel (PSC) dans les Bour Aurélien, Astafieff Katia p.46 collections tropicales des Conservatoire et jar- dins botaniques de Nancy (CJBN) The cultivation method of Welwitschia mirabilis Kazimierczak-Grygiel Ewa p.51 Hook.f. in rhizoboxes THEME A ACCESS TO GENETIC RESOURCES AND BENEFIT-SHARING : STRATEGIC p.58 A3 INTERNATIONAL, EUROPEAN AND NATIONAL LEGISLATIVE FRAMEWORKS AND BEST APPROACHES AND THEIR IMPLICATIONS FOR BOTANIC GARDENS PRACTICE FOR BOTANIC GARDENS The International Plant Exchange Network (IPEN) Kiehn Michael, Löhne Conny p.58 and the Nagoya Protocol Where living collections and convention regula- van den Wollenberg Bert p.65 tions meet. A need for strengthening network- ing within the botanic garden community Implementing the Nagoya Protocol: developing Williams China, Sharrock Suzanne p.80 a toolkit for your botanic garden DATABASES AND BIODIVERSITY p.89 A4 INFORMATION MANAGEMENT A4A PLANT COLLECTION MANAGEMENT SYSTEMS 44 TABLE ↓OF CONTENTS MANAGING INFORMATION ON BIOLOGICAL p.89 A4B DIVERSITY AT ALL LEVELS World Flora Online mid-term update : Loizeau Pierre-André, Wyse Jackson Peter p.89 Flore Mondiale en Ligne pour 2020 The INPN (National Inventory of Natural Heri- Oulès Emeline, Robert Solène, Poncet Laurent, tage), a management tool for French biodiversi- Tercerie Sandrine p.99 ty knowledge dissemination and conservation: the example of Flora and habitat THEME A STRATEGIC FRAMEWORKS AND BEST PRACTICE FOR BOTANIC GARDENS 45 THEME A : STRATEGIC FRAMEWORKS AND BEST EUROGARD VII PRACTICE FOR BOTANIC GARDENS PARIS 01. -
The Evolution of Pollinator–Plant Interaction Types in the Araceae
BRIEF COMMUNICATION doi:10.1111/evo.12318 THE EVOLUTION OF POLLINATOR–PLANT INTERACTION TYPES IN THE ARACEAE Marion Chartier,1,2 Marc Gibernau,3 and Susanne S. Renner4 1Department of Structural and Functional Botany, University of Vienna, 1030 Vienna, Austria 2E-mail: [email protected] 3Centre National de Recherche Scientifique, Ecologie des Foretsˆ de Guyane, 97379 Kourou, France 4Department of Biology, University of Munich, 80638 Munich, Germany Received August 6, 2013 Accepted November 17, 2013 Most plant–pollinator interactions are mutualistic, involving rewards provided by flowers or inflorescences to pollinators. An- tagonistic plant–pollinator interactions, in which flowers offer no rewards, are rare and concentrated in a few families including Araceae. In the latter, they involve trapping of pollinators, which are released loaded with pollen but unrewarded. To understand the evolution of such systems, we compiled data on the pollinators and types of interactions, and coded 21 characters, including interaction type, pollinator order, and 19 floral traits. A phylogenetic framework comes from a matrix of plastid and new nuclear DNA sequences for 135 species from 119 genera (5342 nucleotides). The ancestral pollination interaction in Araceae was recon- structed as probably rewarding albeit with low confidence because information is available for only 56 of the 120–130 genera. Bayesian stochastic trait mapping showed that spadix zonation, presence of an appendix, and flower sexuality were correlated with pollination interaction type. In the Araceae, having unisexual flowers appears to have provided the morphological precon- dition for the evolution of traps. Compared with the frequency of shifts between deceptive and rewarding pollination systems in orchids, our results indicate less lability in the Araceae, probably because of morphologically and sexually more specialized inflorescences. -
Full of Beans: a Study on the Alignment of Two Flowering Plants Classification Systems
Full of beans: a study on the alignment of two flowering plants classification systems Yi-Yun Cheng and Bertram Ludäscher School of Information Sciences, University of Illinois at Urbana-Champaign, USA {yiyunyc2,ludaesch}@illinois.edu Abstract. Advancements in technologies such as DNA analysis have given rise to new ways in organizing organisms in biodiversity classification systems. In this paper, we examine the feasibility of aligning two classification systems for flowering plants using a logic-based, Region Connection Calculus (RCC-5) ap- proach. The older “Cronquist system” (1981) classifies plants using their mor- phological features, while the more recent Angiosperm Phylogeny Group IV (APG IV) (2016) system classifies based on many new methods including ge- nome-level analysis. In our approach, we align pairwise concepts X and Y from two taxonomies using five basic set relations: congruence (X=Y), inclusion (X>Y), inverse inclusion (X<Y), overlap (X><Y), and disjointness (X!Y). With some of the RCC-5 relationships among the Fabaceae family (beans family) and the Sapindaceae family (maple family) uncertain, we anticipate that the merging of the two classification systems will lead to numerous merged solutions, so- called possible worlds. Our research demonstrates how logic-based alignment with ambiguities can lead to multiple merged solutions, which would not have been feasible when aligning taxonomies, classifications, or other knowledge or- ganization systems (KOS) manually. We believe that this work can introduce a novel approach for aligning KOS, where merged possible worlds can serve as a minimum viable product for engaging domain experts in the loop. Keywords: taxonomy alignment, KOS alignment, interoperability 1 Introduction With the advent of large-scale technologies and datasets, it has become increasingly difficult to organize information using a stable unitary classification scheme over time. -
THE INFLUENCE of SELECTED GROWTH REGULATORS on DEVELOPMENT, DECORATIVE VALUE and YIELD of CORMS of EASY POT FREESIA (Freesia Eckl
Acta Sci. Pol., Hortorum Cultus 12(1) 2013, 55-64 THE INFLUENCE OF SELECTED GROWTH REGULATORS ON DEVELOPMENT, DECORATIVE VALUE AND YIELD OF CORMS OF EASY POT FREESIA (Freesia Eckl. ex Klatt). PART I. GIBBERELLIN A3 Piotr ĩurawik, Monika Placek West Pomeranian University of Technology in Szczecin Abstract. Freesias of Easy Pot group are very interesting complement to an assortment of flowering potted plants. However , there is a lack of information about their requirements and cultivation methods. Experiments were carried out in the years 2006–2007 in the un- heated plastic tunnel. Cormlets of three cultivars: ‘Gompey’, ‘Popey’ and ‘Suzy’ were the plant material. Corms were soaked in solution of gibberellic acid in concentration of 10, 20, 40, 80 or 160 mg dm-3 for 24 hours just before planting, in a dark room with air tem- perature 28–30oC. Corms soaked in water were served as the control. During the vegeta- tion season measurements of vegetative and generative traits of plants were conducted. After the end of vegetation period, coefficients of corm weight and number increase were calculated. It was found that cormlets of Easy Pot Freesia can be recommended for culti- vation in pots. Cultivar had a significant effect on vegetative and generative parameters of plants. Among evaluated cultivars ‘Gompey’ was characterized by the greatest decorative value. Plants of this cultivar had the longest inflorescence shoots with the greatest number of lateral shoots and the greatest number of flowers. Irrespective of cultivar, gibberellic acid increased plant height, total number of leaves, length of inflorescence shoots and de- creased flower diameter.