Titan Arum Overview
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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. -
Amorphophallus Paeoniifolius) Cultivated in Java
Yuzammi, Tri Handayani. 2019 P.11 Analysis of Nutrient and Anti-Nutrient Compositions of “Suweg” (Amorphophallus paeoniifolius) Cultivated in Java Yuzammi a1 and Tri Handayania a Research Center for Plant Conservation and Botanic Gardens – Indonesian Institute of Sciences Jl. Ir. H. Juanda no. 13 Bogor (16122), Indonesia Abstract Amorphophallus paeoniifolius (Dennts.) Nicolson belongs to the family Araceae. It is also known as elephant foot yam or suweg, notably for the Javanese. It is a common species in Java and is cultivated for its edible tubers. The suweg tubers used for this research were collected from Kuningan (West Java), Yogyakarta and Kediri (East Java). The study aimed to elucidate the nutrient and anti-nutrient compositions of suweg’s tuber, including carbohydrate, fat, proteins and minerals viz. Ca, Fe and P. The Kjeldhal method was used for protein determination, soxhlet extraction method for lipids, spectrophotometer method for carbohydrate, and Atomic Absorption Spectrophotometer method was used for mineral elements. Anti-nutrient contents determinated were Ca Oxalate and HCN using spectrophotometer method. Both fresh tuber and flour powder of suweg were analysed to indicate the highest percentage of Ca Oxalate content. The results showed that nutrient contents of suweg were carbohydrate 87.02 %, protein 7.08 % and fat 0.18%. These indicated that suweg has high carbohydrate and low fat contents; therefore it is suitable for dietary therapy. The concentration of anti-nutrient, such as Ca Oxalate was lower on the flour powder (0.01 %) rather than fresh tuber (0,21 %). This means the tuber of suweg was not harmful to consume after being processed. -
Flower Development and Its Implication for Seed Production on Amorphophallus Muelleri Blume (Araceae)
J. Hort. Indonesia 7(2): 65-74. Agustus 2016. Flower Development and Its Implication for Seed Production on Amorphophallus muelleri Blume (Araceae) Edi Santosa1,2*, Adolf Pieter Lontoh1, Ani Kurniawati1, Maryati Sari1 and Nobuo Sugiyama3 Diterima 18 Maret 2016/Disetujui 06 Juli 2016 ABSTRACT There are many studies on agronomic and economic advantages of iles-iles (Amorphophallus muelleri Blume), leading to high demand on seed to support the rapid production expansion in many Asian countries. By contrast, there are few studies on flowering phenology and flower morphology although they affect the seed production. Therefore, we evaluated flowering phenology and flower morphology of 80 plants of A. muelleri grown in a field under 65% artificial shading net at Leuwikopo Experimental Farm IPB Darmaga, Bogor, Indonesia from May 2015 to July 2016 in order to improve seed production. A. muelleri produced solitary spadix, with female flowers at the lower part and male flowers at the upper part. Spadix grew slowly for 56-71 days after bud break, and then grew rapidly thereafter for 30-35 days until anthesis. Seed was harvested 9.6 to 10.2 months after anthesis. We devided the development of spadix into seven phases, bud break as stage I and berry maturity as stage VII. Stage VI to VII determined seed production. Seed production was also affected by root formation and spadix size. There were strong positive correlations between length of the female zones with berry production. Some morphological characteristics of spadix were dependent on corm size, thus, it was likely that agronomic improvement to enhance female flower and corm sizes was important in seed production. -
Well-Known Plants in Each Angiosperm Order
Well-known plants in each angiosperm order This list is generally from least evolved (most ancient) to most evolved (most modern). (I’m not sure if this applies for Eudicots; I’m listing them in the same order as APG II.) The first few plants are mostly primitive pond and aquarium plants. Next is Illicium (anise tree) from Austrobaileyales, then the magnoliids (Canellales thru Piperales), then monocots (Acorales through Zingiberales), and finally eudicots (Buxales through Dipsacales). The plants before the eudicots in this list are considered basal angiosperms. This list focuses only on angiosperms and does not look at earlier plants such as mosses, ferns, and conifers. Basal angiosperms – mostly aquatic plants Unplaced in order, placed in Amborellaceae family • Amborella trichopoda – one of the most ancient flowering plants Unplaced in order, placed in Nymphaeaceae family • Water lily • Cabomba (fanwort) • Brasenia (watershield) Ceratophyllales • Hornwort Austrobaileyales • Illicium (anise tree, star anise) Basal angiosperms - magnoliids Canellales • Drimys (winter's bark) • Tasmanian pepper Laurales • Bay laurel • Cinnamon • Avocado • Sassafras • Camphor tree • Calycanthus (sweetshrub, spicebush) • Lindera (spicebush, Benjamin bush) Magnoliales • Custard-apple • Pawpaw • guanábana (soursop) • Sugar-apple or sweetsop • Cherimoya • Magnolia • Tuliptree • Michelia • Nutmeg • Clove Piperales • Black pepper • Kava • Lizard’s tail • Aristolochia (birthwort, pipevine, Dutchman's pipe) • Asarum (wild ginger) Basal angiosperms - monocots Acorales -
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 -
Understanding the Origin and Rapid Diversification of the Genus Anthurium Schott (Araceae), Integrating Molecular Phylogenetics, Morphology and Fossils
University of Missouri, St. Louis IRL @ UMSL Dissertations UMSL Graduate Works 8-3-2011 Understanding the origin and rapid diversification of the genus Anthurium Schott (Araceae), integrating molecular phylogenetics, morphology and fossils Monica Maria Carlsen University of Missouri-St. Louis, [email protected] Follow this and additional works at: https://irl.umsl.edu/dissertation Part of the Biology Commons Recommended Citation Carlsen, Monica Maria, "Understanding the origin and rapid diversification of the genus Anthurium Schott (Araceae), integrating molecular phylogenetics, morphology and fossils" (2011). Dissertations. 414. https://irl.umsl.edu/dissertation/414 This Dissertation is brought to you for free and open access by the UMSL Graduate Works at IRL @ UMSL. It has been accepted for inclusion in Dissertations by an authorized administrator of IRL @ UMSL. For more information, please contact [email protected]. Mónica M. Carlsen M.S., Biology, University of Missouri - St. Louis, 2003 B.S., Biology, Universidad Central de Venezuela – Caracas, 1998 A Thesis Submitted to The Graduate School at the University of Missouri – St. Louis in partial fulfillment of the requirements for the degree Doctor of Philosophy in Biology with emphasis in Ecology, Evolution and Systematics June 2011 Advisory Committee Peter Stevens, Ph.D. (Advisor) Thomas B. Croat, Ph.D. (Co-advisor) Elizabeth Kellogg, Ph.D. Peter M. Richardson, Ph.D. Simon J. Mayo, Ph.D Copyright, Mónica M. Carlsen, 2011 Understanding the origin and rapid diversification of the genus Anthurium Schott (Araceae), integrating molecular phylogenetics, morphology and fossils Mónica M. Carlsen M.S., Biology, University of Missouri - St. Louis, 2003 B.S., Biology, Universidad Central de Venezuela – Caracas, 1998 Advisory Committee Peter Stevens, Ph.D. -
Ex Situ Conservation of Amorphophallus Titanum in Bogor Botanic Gardens, Indonesia
PROS SEM NAS MASY BIODIV INDON Volume 2, Nomor 2, Desember 2016 ISSN: 2407-8050 Halaman: 219-225 DOI: 10.13057/psnmbi/m020217 Ex situ conservation of Amorphophallus titanum in Bogor Botanic Gardens, Indonesia Konservasi ex situ Amorphophallus titanum di Kebun Raya Bogor, Indonesia DWI MURTI PUSPITANINGTYAS♥, SITI ROOSITA ARIATI Centre for Plant Conservation Botanic Gardens (Bogor Botanic Gardens), Indonesian Institute of Sciences. Jl. Ir. H. Juanda No. 13 Bogor 16122, Jawa Barat. Tel./Fax. 0251-8322-187, ♥email: [email protected] Manuscript received: 3 November 2016. Revision accepted: 17 December 2016. Abstract. Puspitaningtyas DM, Ariati SR. 2016. Ex situ conservation of Amorphophallus titanum in Bogor Botanic Gardens, Indonesia. Pros Sem Nas Masy Biodiv Indon 2: 219-225. Titan Arum (Amorphophallus titanum (Becc.) Becc.) merupakan tanaman asli dan endemik Sumatera. Tumbuhan ini pertama kali ditemukan pada tahun 1878 oleh ahli botani Florentine (Italia) yang bernama Odoardo Beccari. Perbungaannya yang berukuran raksasa dianggap menarik, sehingga Kebun Raya Bogor menjadikan tumbuhan ini sebagai jenis unggulan. Titan Arum secara alami tumbuh di hutan hujan atau perkebunan/pekarangan penduduk lokal. Di alam liar, habitat alami Titan Arum telah rusak akibat tekanan jumlah penduduk yang terus meningkat, atau banyak dibabat oleh penduduk karena dianggap sebagai gulma. Selain itu, degradasi hutan akibat pembalakan liar oleh penduduk juga menjadi ancaman lain bagi habitat tumbuhan tersebut. Kebun Raya Bogor telah memainkan peranan yang penting dalam konservasi A. titanum secara ex situ. Tumbuhan ini telah dikembangkan sejak tahun 1954 sebagai upaya konservasi ex situ. Kajian ini menampilkan data sekunder A. titanum yang berasal dari database koleksi tumbuhan Kebun Raya Bogor. -
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. -
Indigenous Plants of Bendigo
Produced by Indigenous Plants of Bendigo Indigenous Plants of Bendigo PMS 1807 RED PMS 432 GREY PMS 142 GOLD A Gardener’s Guide to Growing and Protecting Local Plants 3rd Edition 9 © Copyright City of Greater Bendigo and Bendigo Native Plant Group Inc. This work is Copyright. Apart from any use permitted under the Copyright Act 1968, no part may be reproduced by any process without prior written permission from the City of Greater Bendigo. First Published 2004 Second Edition 2007 Third Edition 2013 Printed by Bendigo Modern Press: www.bmp.com.au This book is also available on the City of Greater Bendigo website: www.bendigo.vic.gov.au Printed on 100% recycled paper. Disclaimer “The information contained in this publication is of a general nature only. This publication is not intended to provide a definitive analysis, or discussion, on each issue canvassed. While the Committee/Council believes the information contained herein is correct, it does not accept any liability whatsoever/howsoever arising from reliance on this publication. Therefore, readers should make their own enquiries, and conduct their own investigations, concerning every issue canvassed herein.” Front cover - Clockwise from centre top: Bendigo Wax-flower (Pam Sheean), Hoary Sunray (Marilyn Sprague), Red Ironbark (Pam Sheean), Green Mallee (Anthony Sheean), Whirrakee Wattle (Anthony Sheean). Table of contents Acknowledgements ...............................................2 Foreword..........................................................3 Introduction.......................................................4 -
Ongoing Evolution in the Genus Crocus: Diversity of Flowering Strategies on the Way to Hysteranthy
plants Article Ongoing Evolution in the Genus Crocus: Diversity of Flowering Strategies on the Way to Hysteranthy Teresa Pastor-Férriz 1, Marcelino De-los-Mozos-Pascual 1, Begoña Renau-Morata 2, Sergio G. Nebauer 2 , Enrique Sanchis 2, Matteo Busconi 3 , José-Antonio Fernández 4, Rina Kamenetsky 5 and Rosa V. Molina 2,* 1 Departamento de Gestión y Conservación de Recursos Fitogenéticos, Centro de Investigación Agroforestal de Albadaledejito, 16194 Cuenca, Spain; [email protected] (T.P.-F.); [email protected] (M.D.-l.-M.-P.) 2 Departamento de Producción Vegetal, Universitat Politècnica de València, 46022 Valencia, Spain; [email protected] (B.R.-M.); [email protected] (S.G.N.); [email protected] (E.S.) 3 Department of Sustainable Crop Production, Università Cattolica del Sacro Cuore, 29122 Piacenza, Italy; [email protected] 4 IDR-Biotechnology and Natural Resources, Universidad de Castilla-La Mancha, 02071 Albacete, Spain; [email protected] 5 Department of Ornamental Horticulture and Biotechnology, The Volcani Center, ARO, Rishon LeZion 7505101, Israel; [email protected] * Correspondence: [email protected] Abstract: Species of the genus Crocus are found over a wide range of climatic areas. In natural habitats, these geophytes diverge in the flowering strategies. This variability was assessed by analyzing the flowering traits of the Spanish collection of wild crocuses, preserved in the Bank of Plant Germplasm Citation: Pastor-Férriz, T.; of Cuenca. Plants of the seven Spanish species were analyzed both in their natural environments De-los-Mozos-Pascual, M.; (58 native populations) and in common garden experiments (112 accessions). -
Plant Life of Western Australia
INTRODUCTION The characteristic features of the vegetation of Australia I. General Physiography At present the animals and plants of Australia are isolated from the rest of the world, except by way of the Torres Straits to New Guinea and southeast Asia. Even here adverse climatic conditions restrict or make it impossible for migration. Over a long period this isolation has meant that even what was common to the floras of the southern Asiatic Archipelago and Australia has become restricted to small areas. This resulted in an ever increasing divergence. As a consequence, Australia is a true island continent, with its own peculiar flora and fauna. As in southern Africa, Australia is largely an extensive plateau, although at a lower elevation. As in Africa too, the plateau increases gradually in height towards the east, culminating in a high ridge from which the land then drops steeply to a narrow coastal plain crossed by short rivers. On the west coast the plateau is only 00-00 m in height but there is usually an abrupt descent to the narrow coastal region. The plateau drops towards the center, and the major rivers flow into this depression. Fed from the high eastern margin of the plateau, these rivers run through low rainfall areas to the sea. While the tropical northern region is characterized by a wet summer and dry win- ter, the actual amount of rain is determined by additional factors. On the mountainous east coast the rainfall is high, while it diminishes with surprising rapidity towards the interior. Thus in New South Wales, the yearly rainfall at the edge of the plateau and the adjacent coast often reaches over 100 cm. -
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.