A Review on Tibouchina Urvilleana (DC.) Cogn
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Status, Ecology, and Management of the Invasive Plant, Miconia Calvescens DC (Melastomataceae) in the Hawaiian Islands1
Records of the Hawaii Biological Survey for 1996. Bishop 23 Museum Occasional Papers 48: 23-36. (1997) Status, Ecology, and Management of the Invasive Plant, Miconia calvescens DC (Melastomataceae) in the Hawaiian Islands1 A.C. MEDEIROS2, L.L. LOOPE3 (United States Geological Survey, Biological Resources Division, Haleakala National Park Field Station, P.O. Box 369, Makawao, HI 96768, USA), P. CONANT (Hawaii Department of Agriculture, 1428 South King St., P.O. Box 22159, Honolulu, HI 96823, USA), & S. MCELVANEY (Hawaii Natural Heritage Program/The Nature Conservancy of Hawaii, 1116 Smith St., Suite 201, Honolulu, HI 96817, USA) Abstract Miconia calvescens (Melastomataceae), native to montane forests of the neotropics, has now invaded wet forests of both the Society and Hawaiian Islands. This tree, which grows up to 15 m tall, is potentially the most invasive and damaging weed of rainforests of Pacific islands. In moist conditions, it grows rapidly, tolerates shade, and produces abundant seed that is effectively dispersed by birds and accumulates in a large, persistent soil seed-bank. Introduced to the Hawaiian Islands in 1961, M. calvescens appears to threaten much of the biological diversity in native forests receiving 1800–2000 mm or more annual precipitation. Currently, M. calvescens is found on 4 Hawaiian islands— Hawaii, Maui, Oahu, and Kauai. Widespread awareness of this invader began in the early 1990s. Although biological control is being pursued, conventional control techniques (mechanical and chemical) to contain and eradicate it locally are underway. Introduction The effects of biological invasions are increasingly being recognized for their role in degradation of biological diversity worldwide (Usher et al., 1988; D’Antonio & Vitousek, 1992). -
HEAR HNIS Report on Miconia Calvescens
Saturday, March 29, 1997 HNIS Report for Miconia calvescens Page 1 A product of the Hawaiian Ecosystems at Risk Project Miconia calvescens DC. Miconia calvescens, in the melastome family (Melastomataceae), is a tree 4-15 m tall with large (to 80 cm in length), strongly trinerved leaves, dark-green above and purple below. Federal Noxious Weed? N Hawaii State Noxious Weed? Y Federal Seed Act? N Hawaii State Seed Act? N [illustration source: unknown] Native to where : The native range of Miconia calvescens extends from 20 degrees N in Mexico, Guatemala, and Belize to 20 degrees S in Brazil and Argentina (Meyer 1994). The upper elevational limit of the species in its native range is 1830 m in Ecuador (Wurdack 1980). Meyer (1994) determined that the form with very large leaves with purple leaf undersides occurs only in Mexico, Guatemala, Belize, and Costa Rica; specimens examined by Meyer were collected at elevations between 45 m and 1400 m. Native climate : The climate in which Miconia calvescens occurs is tropical montane. Based on its ecology in Tahiti and its occurrence to 1830 m in Ecuador, it appears to pose a threat to all habitats below the upper forest line which receive 1800-2000 mm (75-80 inches) or more of annual precipitation. Biology and ecology : Phenology: Flowering and fruiting of mature trees in Miconia calvescens populations in Hawaii appear to be somewhat synchronized and may be triggered by weather events (drought and/or rain). A single tree can flower/fruit 2-3 times in a year. A single flowering/fruiting event is prolonged, and all stages and mature and immature fruits are often seen on a single tree. -
Phylogeny and Classification of the Melastomataceae and Memecylaceae
Nord. J. Bot. - Section of tropical taxonomy Phylogeny and classification of the Melastomataceae and Memecy laceae Susanne S. Renner Renner, S. S. 1993. Phylogeny and classification of the Melastomataceae and Memecy- laceae. - Nord. J. Bot. 13: 519-540. Copenhagen. ISSN 0107-055X. A systematic analysis of the Melastomataceae, a pantropical family of about 4200- 4500 species in c. 166 genera, and their traditional allies, the Memecylaceae, with c. 430 species in six genera, suggests a phylogeny in which there are two major lineages in the Melastomataceae and a clearly distinct Memecylaceae. Melastomataceae have close affinities with Crypteroniaceae and Lythraceae, while Memecylaceae seem closer to Myrtaceae, all of which were considered as possible outgroups, but sister group relationships in this plexus could not be resolved. Based on an analysis of all morph- ological and anatomical characters useful for higher level grouping in the Melastoma- taceae and Memecylaceae a cladistic analysis of the evolutionary relationships of the tribes of the Melastomataceae was performed, employing part of the ingroup as outgroup. Using 7 of the 21 characters scored for all genera, the maximum parsimony program PAUP in an exhaustive search found four 8-step trees with a consistency index of 0.86. Because of the limited number of characters used and the uncertain monophyly of some of the tribes, however, all presented phylogenetic hypotheses are weak. A synapomorphy of the Memecylaceae is the presence of a dorsal terpenoid-producing connective gland, a synapomorphy of the Melastomataceae is the perfectly acrodro- mous leaf venation. Within the Melastomataceae, a basal monophyletic group consists of the Kibessioideae (Prernandra) characterized by fiber tracheids, radially and axially included phloem, and median-parietal placentation (placentas along the mid-veins of the locule walls). -
Pollination Ecology Summary
Pollination Ecology Summary Prof. em. Klaus Ammann, Neuchâtel [email protected] June 2013 Ohne den Pollenübertragungs-Service blütenbesuchender Tiere könnten sich viele Blütenpanzen nicht geschlechtlich fortpanzen. Die komplexen und faszinierenden Bestäubungsvorgänge bei Blütenpanzen sind Ausdruck von Jahrmillionen von Selektionsvorgängen, verbunden mit Selbstorganisation der Lebewesen; eine Sicht, die auch Darwin schon unterstützte. Bei vielen zwischenartlichen Beziehungen haben sich zwei oder auch mehrere Arten in ihrer Entwicklung gegenseitig beeinusst. Man spricht hier von sogenannter Coevolution. Deutlich ist die Coevolution auch bei verschiedenen Bestäubungssystemen und -mechanismen, die von symbiontischer bis parasitischer Natur sein können. Die Art-Entstehung, die Vegetationsökologie und die Entstehung von Kulturpanzen sind eng damit verbunden Veranstalter: Naturforschende Gesellschaft Schaffhausen 1. Pollination Ecology Darwin http://en.wikipedia.org/wiki/Pollination_syndrome http://www.cas.vanderbilt.edu/bioimages/pages/pollination.htm Fenster, C.B., Armbruster, W.S., Wilson, P., Dudash, M.R., & Thomson, J.D. (2004) Pollination syndromes and floral specialization. Annual Review of Ecology Evolution and Systematics, 35, pp 375-403 http://www.botanischergarten.ch/Pollination/Fenster-Pollination-Syndromes-2004.pdf invitation to browse in the website of the Friends of Charles Darwin http://darwin.gruts.com/weblog/archive/2008/02/ Working Place of Darwin in Downe Village http://www.focus.de/wissen/wissenschaft/wissenschaft-darwin-genoss-ein-suesses-studentenleben_aid_383172.html Darwin as a human being and as a scientist Darwin, C. (1862), On the various contrivances by which orchids are fertilized by insects and on the good effects of intercrossing The Complete Work of Charles Darwin online, Scanned, OCRed and corrected by John van Wyhe 2003; further corrections 8.2006. -
MELASTOMATACEAE 野牡丹科 Ye Mu Dan Ke Chen Jie (陈介 Chen Cheih)1; Susanne S
MELASTOMATACEAE 野牡丹科 ye mu dan ke Chen Jie (陈介 Chen Cheih)1; Susanne S. Renner2 Herbs, shrubs, or trees (to 20 m tall), erect, climbing, or rarely epiphytic. Stipules lacking. Leaves simple, commonly opposite and decussate with one of a pair slightly smaller than other, rarely verticillate or alternate by abortion of one of a pair, usually 1–4(or 5) secondary veins on each side of midvein, originating at or near base and anastomosing apically, tertiary veins numerous, parallel, and connecting secondary veins and midvein but in Memecylon secondary veins pinnate and tertiary veins reticulate. Inflorescences cymose, umbellate, corymbose, in paniculate clusters, or a cincinnus, rarely flowers single, fascicled, or born on a spike; bracts sometimes conspicuous and persistent. Flowers bisexual, actinomorphic but androecium often slightly zygomorphic, usually (3 or)4- or 5(or 6)-merous, perianth biseriate, perigynous; bracteoles opposite, usually caducous. Hypanthium funnel-shaped, campanulate, cyathiform, or urceolate. Calyx lobes (3–)5(or 6), valvate (rarely connate, but not in Chinese species). Petals (3–)5(or 6), equal to number of sepals, distinct, imbricate. Stamens usually twice as many as petals and in 2 whorls, rarely as many as petals by loss of 1 whorl, isomorphic or dimorphic; filaments distinct, often geniculate, inflexed in bud; anthers typically 2-celled, introrse, basifixed, dehiscent by 1 or 2 apical pores or by short longitudinal slits (Astronia, Memecylon); connective often variously appendaged. Pistil and style 1; stigma minute, capitate or truncate. Ovary commonly inferior or semi-inferior, locules usually (3 or)4 or 5(or 6) with numerous anatropous ovules, rarely 1-loculed and ovules ca. -
Non-Expressway Master Plant List
MASTER PLANT LIST GENERAL INTRODUCTION TO PLANT LISTS Plants are living organisms. They possess variety in form, foliage and flower color, visual texture and ultimate size. There is variation in plants of the same species. Plants change: with seasons, with time and with the environment. Yet here is an attempt to categorize and catalogue a group of plants well suited for highway and expressway planting in Santa Clara County. This is possible because in all the existing variety of plants, there still remains a visual, morphological and taxonomical distinction among them. The following lists and identification cards emphasize these distinctions. 1 of 6 MASTER PLANT LIST TREES Acacia decurrens: Green wattle Acacia longifolia: Sydney golden wattle Acacia melanoxylon: Blackwood acacia Acer macrophyllum: Bigleaf maple Aesculus californica: California buckeye Aesculus carnea: Red horsechestnut Ailanthus altissima: Tree-of-heaven Albizia julibrissin: Silk tree Alnus cordata: Italian alder Alnus rhombifolia: White alder Arbutus menziesii: Madrone Calocedrus decurrens: Incense cedar Casuarina equisetifolia: Horsetail tree Casuarina stricta: Coast beefwood Catalpa speciosa: Western catalpa Cedrus deodara: Deodar cedar Ceratonia siliqua: Carob Cinnamomum camphora: Camphor Cordyline australis: Australian dracena Crataegus phaenopyrum: Washington thorn Cryptomeria japonica: Japanese redwood Cupressus glabra: Arizona cypress Cupressus macrocarpa: Monterey cypress Eriobotrya japonica: Loquat Eucalyptus camaldulensis: Red gum Eucalyptus citriodora: Lemon-scented -
Information Sheet on Ramsar Wetlands (RIS) – 2009-2012 Version Available for Download From
Information Sheet on Ramsar Wetlands (RIS) – 2009-2012 version Available for download from http://www.ramsar.org/ris/key_ris_index.htm. Categories approved by Recommendation 4.7 (1990), as amended by Resolution VIII.13 of the 8th Conference of the Contracting Parties (2002) and Resolutions IX.1 Annex B, IX.6, IX.21 and IX. 22 of the 9th Conference of the Contracting Parties (2005). Notes for compilers: 1. The RIS should be completed in accordance with the attached Explanatory Notes and Guidelines for completing the Information Sheet on Ramsar Wetlands. Compilers are strongly advised to read this guidance before filling in the RIS. 2. Further information and guidance in support of Ramsar site designations are provided in the Strategic Framework and guidelines for the future development of the List of Wetlands of International Importance (Ramsar Wise Use Handbook 14, 3rd edition). A 4th edition of the Handbook is in preparation and will be available in 2009. 3. Once completed, the RIS (and accompanying map(s)) should be submitted to the Ramsar Secretariat. Compilers should provide an electronic (MS Word) copy of the RIS and, where possible, digital copies of all maps. 1. Name and address of the compiler of this form: FOR OFFICE USE ONLY. DD MM YY Beatriz de Aquino Ribeiro - Bióloga - Analista Ambiental / [email protected], (95) Designation date Site Reference Number 99136-0940. Antonio Lisboa - Geógrafo - MSc. Biogeografia - Analista Ambiental / [email protected], (95) 99137-1192. Instituto Chico Mendes de Conservação da Biodiversidade - ICMBio Rua Alfredo Cruz, 283, Centro, Boa Vista -RR. CEP: 69.301-140 2. -
A Field Guide to the Early Detection of Invasive Plants and Animals on Kaua‘I, Hawai‘I Acknowledgements
‘‘ A Field Guide to the Early Detection of Invasive Plants and Animals on Kaua‘i, Hawai‘i Acknowledgements Early Detection Field Guide Development Tiffani Keanini Kaua‘i Invasive Species Committee Elizabeth Speith USGS NBII Pacific Basin Information Node Keren Gundersen Kaua‘i Invasive Species Committee Content & Review Forest & Kim Starr United States Geological Survey Hawai‘i Invasive Species Council Kaua‘i Invasive Species Committee Maui Invasive Species Committee USGS NBII Pacific Basin Information Node Illustrations Brooke Mahnken Maui Invasive Species Committee Special thanks to the Hawai‘i Invasive Species Council for providing the funds to print this field guide. April 2010 Table of Contents Quick Reference Guide ...................................................................A The Need for Your Eyes & Ears .....................................................1 How to Use this Field Guide .............................................................2 What are we protecting? .................................................................3 What Makes a Species Invasive in Hawai‘i?. ..............................3 Plant Species. .................................................................................................4-31 Invertebrate Species ..................................................................32-35 Animal Species ..........................................................................36-41 Snakes and other animals.......................................................42-43 What You Can Do to Protect Kauai -
Systematics and Relationships of Tryssophyton (Melastomataceae
A peer-reviewed open-access journal PhytoKeys 136: 1–21 (2019)Systematics and relationships of Tryssophyton (Melastomataceae) 1 doi: 10.3897/phytokeys.136.38558 RESEARCH ARTICLE http://phytokeys.pensoft.net Launched to accelerate biodiversity research Systematics and relationships of Tryssophyton (Melastomataceae), with a second species from the Pakaraima Mountains of Guyana Kenneth J. Wurdack1, Fabián A. Michelangeli2 1 Department of Botany, MRC-166 National Museum of Natural History, Smithsonian Institution, P.O. Box 37012, Washington, DC 20013-7012, USA 2 The New York Botanical Garden, 2900 Southern Blvd., Bronx, NY 10458, USA Corresponding author: Kenneth J. Wurdack ([email protected]) Academic editor: Ricardo Kriebel | Received 25 July 2019 | Accepted 30 October 2019 | Published 10 December 2019 Citation: Wurdack KJ, Michelangeli FA (2019) Systematics and relationships of Tryssophyton (Melastomataceae), with a second species from the Pakaraima Mountains of Guyana. PhytoKeys 136: 1–21. https://doi.org/10.3897/ phytokeys.136.38558 Abstract The systematics of Tryssophyton, herbs endemic to the Pakaraima Mountains of western Guyana, is re- viewed and Tryssophyton quadrifolius K.Wurdack & Michelang., sp. nov. from the summit of Kamakusa Mountain is described as the second species in the genus. The new species is distinguished from its closest relative, Tryssophyton merumense, by striking vegetative differences, including number of leaves per stem and leaf architecture. A phylogenetic analysis of sequence data from three plastid loci and Melastomata- ceae-wide taxon sampling is presented. The two species of Tryssophyton are recovered as monophyletic and associated with mostly Old World tribe Sonerileae. Fruit, seed and leaf morphology are described for the first time, biogeography is discussed and both species are illustrated. -
Recommendation of Native Species for the Reforestation of Degraded Land Using Live Staking in Antioquia and Caldas’ Departments (Colombia)
UNIVERSITÀ DEGLI STUDI DI PADOVA Department of Land, Environment Agriculture and Forestry Second Cycle Degree (MSc) in Forest Science Recommendation of native species for the reforestation of degraded land using live staking in Antioquia and Caldas’ Departments (Colombia) Supervisor Prof. Lorenzo Marini Co-supervisor Prof. Jaime Polanía Vorenberg Submitted by Alicia Pardo Moy Student N. 1218558 2019/2020 Summary Although Colombia is one of the countries with the greatest biodiversity in the world, it has many degraded areas due to agricultural and mining practices that have been carried out in recent decades. The high Andean forests are especially vulnerable to this type of soil erosion. The corporate purpose of ‘Reforestadora El Guásimo S.A.S.’ is to use wood from its plantations, but it also follows the parameters of the Forest Stewardship Council (FSC). For this reason, it carries out reforestation activities and programs and, very particularly, it is interested in carrying out ecological restoration processes in some critical sites. The study area is located between 2000 and 2750 masl and is considered a low Andean humid forest (bmh-MB). The average annual precipitation rate is 2057 mm and the average temperature is around 11 ºC. The soil has a sandy loam texture with low pH, which limits the amount of nutrients it can absorb. FAO (2014) suggests that around 10 genera are enough for a proper restoration. After a bibliographic revision, the genera chosen were Alchornea, Billia, Ficus, Inga, Meriania, Miconia, Ocotea, Protium, Prunus, Psidium, Symplocos, Tibouchina, and Weinmannia. Two inventories from 2013 and 2019, helped to determine different biodiversity indexes to check the survival of different species and to suggest the adequate characteristics of the individuals for a successful vegetative stakes reforestation. -
Effect of Light and Temperature on Seed Germination in Tibouchina Mutabilis (Vell.) Cogn. (Melastomataceae)
Biota Neotrop., vol. 8, no. 2, Abr./Jun. 2008 Effect of light and temperature on seed germination in Tibouchina mutabilis (Vell.) Cogn. (Melastomataceae) Edson Simão1 & Massanori Takaki1,2 1Departamento de Botânica, Instituto de Biociências, Universidade Estadual Paulista – UNESP, CEP 13506-900, CP 199, Rio Claro, SP, Brazil 2Corresponding author: Massanori Takaki, e-mail: [email protected] SIMÃO, E. & TAKAKI, M. 2008. Effect of light and temperature on seed germination in Tibouchina mutabilis (Vell.) Cogn. (Melastomataceae). Biota Neotrop. 8(2): http://www.biotaneotropica.org.br/v8n2/en/ abstract?article+bn00908022008. Abstract: The effect of light and temperature on Tibouchina mutabilis seed germination was analyzed by isothermic incubations in the range of 10 to 40 °C, with 5 °C intervals under both continuous white light (32.85 Mmolm–2s–1) and darkness and alternating temperatures (15-20; 15-25; 15-30; 15-35; 20-25; 20-30; 20-35; 25-30; 25-35 and 30-35 °C) under both photoperiod of 12 hours and continuous darkness. The seeds of T. mutabilis need light to trigger the germination and no germination was observed in darkness. The range of optimum temperatures for germination was between 25 to 30 °C and the 20-25 °C alternating temperatures. These results indicate that T. mutabilis behaves as a pioneer species and daily alternating temperatures did not change the light sensitivity of seeds. Keywords: light, phytochrome, seed germination, Tibouchina. SIMÃO, E. & TAKAKI, M. 2008. Efeito da luz e da temperatura na germinação de sementes de Tibouchina mutabilis (Vell.) Cogn. (Melastomataceae). Biota Neotrop. 8(2): http://www.biotaneotropica.org.br/v8n2/pt/ abstract?article+bn00908022008. -
Tibouchina Urvilleana: Princess-Flower1 Edward F
ENH791 Tibouchina urvilleana: Princess-Flower1 Edward F. Gilman and Dennis G. Watson2 Introduction This sprawling, evergreen shrub or small ornamental tree ranges from 10 to 15 feet (20 feet with proper training) in height. It can be trimmed to any size and still put on a vivid, year-long flower display. The dark green, velvety, four to six-inch-long leaves have several prominent longitudinal veins instead of the usual one, and are often edged in red. Large, royal purple blossoms, flaring open to five inches, are held on terminal panicles above the foliage, creating a spectacular sight when in full bloom. Some flowers are open throughout the year but they are especially plentiful from May to January. Princess-Flower is ideal for the mixed shrubbery border or used in small groupings to compound the impact of bloom-time. General Information Scientific name: Tibouchina urvilleana Pronunciation: tib-oo-KYE-nuh er-vill-ee-AY-nuh Figure 1. Middle-aged Tibouchina urvilleana: Princess-Flower Common name(s): Princess-Flower Family: Melastomataceae Uses: hedge; deck orpatio; screen; specimen; container or USDA hardiness zones: 9B through 11 (Fig. 2) planter; espalier; trained as a standard Origin: not native to North America Availability: not native to North America Invasive potential: has been evaluated using the IFAS Assessment of the Status of Non-Native Plants in Florida’s Description Natural Areas (Fox et al. 2005). This species is not docu- Height: 10 to 15 feet mented in any undisturbed natural areas in Florida. Thus, Spread: 10 to 15 feet it is not considered a problem species and may be used in Crown uniformity: irregular Florida.