A Highly Threatened New Species of Vanilla from Costa Rica Adam P
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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. -
Biodiversity and Evolution in the Vanilla Genus
1 Biodiversity and Evolution in the Vanilla Genus Gigant Rodolphe1,2, Bory Séverine1,2, Grisoni Michel2 and Besse Pascale1 1University of La Reunion, UMR PVBMT 2CIRAD, UMR PVBMT, France 1. Introduction Since the publication of the first vanilla book by Bouriquet (1954c) and the more recent review on vanilla biodiversity (Bory et al., 2008b), there has been a world regain of interest for this genus, as witnessed by the recently published vanilla books (Cameron, 2011a; Havkin-Frenkel & Belanger, 2011; Odoux & Grisoni, 2010). A large amount of new data regarding the genus biodiversity and its evolution has also been obtained. These will be reviewed in the present paper and new data will also be presented. 2. Biogeography, taxonomy and phylogeny 2.1 Distribution and phylogeography Vanilla Plum. ex Miller is an ancient genus in the Orchidaceae family, Vanilloideae sub- family, Vanilleae tribe and Vanillinae sub-tribe (Cameron, 2004, 2005). Vanilla species are distributed throughout the tropics between the 27th north and south parallels, but are absent in Australia. The genus is most diverse in tropical America (52 species), and can also be found in Africa (14 species) and the Indian ocean islands (10 species), South-East Asia and New Guinea (31 species) and Pacific islands (3 species) (Portères, 1954). From floral morphological observations, Portères (1954) suggested a primary diversification centre of the Vanilla genus in Indo-Malaysia, followed by dispersion on one hand from Asia to Pacific and then America, and on the other hand from Madagascar to Africa. This hypothesis was rejected following the first phylogenetic studies of the genus (Cameron, 1999, 2000) which suggested a different scenario with an American origin of the genus (160 to 120 Mya) and a transcontinental migration of the Vanilla genus before the break-up of Gondwana (Cameron, 2000, 2003, 2005; Cameron et al., 1999). -
Angiosperm Latin Name: Brassia Spp. Common Name: Spider Orchid Family: Orchidaceae Geographic Origin: Brazil Soil: Use Orchid Po
Latin Name: Brassia spp. Common Name: Spider Orchid Family: Orchidaceae Geographic Origin: Brazil Soil: Use orchid potting mix. Temperature: Daytime temperatures should be between 75°-85°F and nighttime temperatures should be between 65°-75°F. Light: This plant prefers full sun with partial shade. Moisture: Soak plant in a bucket of water for one hour every week. Fertilization: This plant should be fertilized every other week, alternating between fish and seaweed fertilizers. Grooming: Repot every year or two. Seasonal Care: Reduce watering and fertilizing during winter months. Propagation: Propagate through division or plantlets. Pests and Diseases: Check for root rot, mealy bugs, and whitefly. Angiosperm Latin Name: Dendrobium kingianum Common Name: Pink Rock Orchid Family: Orchidaceae Geographic Origin: Australia Soil: Use orchid potting mix. Temperature: Daytime temperatures should be between 75°-85°F and nighttime temperatures should be between 65°-75°F. Light: This plant prefers full sun with partial shade. Moisture: Soak plant in a bucket of water for one hour every week. Fertilization: This plant should be fertilized every other week, alternating between fish and seaweed fertilizers. Grooming: Repot every year or two. Seasonal Care: Reduce watering and fertilizing during winter months. Propagation: Propagate through division or plantlets. Pests and diseases: Check for root rot, mealy bugs, and whitefly. Angiosperm Latin Name: Dendrobium ‘Wave King’ Common Name: Wave King Orchid Family: Orchidaceae Geographic Origin: South Asia Soil: Use orchid potting mix. Temperature: Daytime temperatures should be between 75°-85°F and nighttime temperatures should be between 65°-75°F. Light: This plant prefers full sun with partial shade. -
Fruits and Seeds of Genera in the Subfamily Faboideae (Fabaceae)
Fruits and Seeds of United States Department of Genera in the Subfamily Agriculture Agricultural Faboideae (Fabaceae) Research Service Technical Bulletin Number 1890 Volume I December 2003 United States Department of Agriculture Fruits and Seeds of Agricultural Research Genera in the Subfamily Service Technical Bulletin Faboideae (Fabaceae) Number 1890 Volume I Joseph H. Kirkbride, Jr., Charles R. Gunn, and Anna L. Weitzman Fruits of A, Centrolobium paraense E.L.R. Tulasne. B, Laburnum anagyroides F.K. Medikus. C, Adesmia boronoides J.D. Hooker. D, Hippocrepis comosa, C. Linnaeus. E, Campylotropis macrocarpa (A.A. von Bunge) A. Rehder. F, Mucuna urens (C. Linnaeus) F.K. Medikus. G, Phaseolus polystachios (C. Linnaeus) N.L. Britton, E.E. Stern, & F. Poggenburg. H, Medicago orbicularis (C. Linnaeus) B. Bartalini. I, Riedeliella graciliflora H.A.T. Harms. J, Medicago arabica (C. Linnaeus) W. Hudson. Kirkbride is a research botanist, U.S. Department of Agriculture, Agricultural Research Service, Systematic Botany and Mycology Laboratory, BARC West Room 304, Building 011A, Beltsville, MD, 20705-2350 (email = [email protected]). Gunn is a botanist (retired) from Brevard, NC (email = [email protected]). Weitzman is a botanist with the Smithsonian Institution, Department of Botany, Washington, DC. Abstract Kirkbride, Joseph H., Jr., Charles R. Gunn, and Anna L radicle junction, Crotalarieae, cuticle, Cytiseae, Weitzman. 2003. Fruits and seeds of genera in the subfamily Dalbergieae, Daleeae, dehiscence, DELTA, Desmodieae, Faboideae (Fabaceae). U. S. Department of Agriculture, Dipteryxeae, distribution, embryo, embryonic axis, en- Technical Bulletin No. 1890, 1,212 pp. docarp, endosperm, epicarp, epicotyl, Euchresteae, Fabeae, fracture line, follicle, funiculus, Galegeae, Genisteae, Technical identification of fruits and seeds of the economi- gynophore, halo, Hedysareae, hilar groove, hilar groove cally important legume plant family (Fabaceae or lips, hilum, Hypocalypteae, hypocotyl, indehiscent, Leguminosae) is often required of U.S. -
PHASEOLUS LESSON ONE PHASEOLUS and the FABACEAE INTRODUCTION to the FABACEAE
1 PHASEOLUS LESSON ONE PHASEOLUS and the FABACEAE In this lesson we will begin our study of the GENUS Phaseolus, a member of the Fabaceae family. The Fabaceae are also known as the Legume Family. We will learn about this family, the Fabaceae and some of the other LEGUMES. When we study about the GENUS and family a plant belongs to, we are studying its TAXONOMY. For this lesson to be complete you must: ___________ do everything in bold print; ___________ answer the questions at the end of the lesson; ___________ complete the world map at the end of the lesson; ___________ complete the table at the end of the lesson; ___________ learn to identify the different members of the Fabaceae (use the study materials at www.geauga4h.org); and ___________ complete one of the projects at the end of the lesson. Parts of the lesson are in underlined and/or in a different print. Younger members can ignore these parts. WORDS PRINTED IN ALL CAPITAL LETTERS may be new vocabulary words. For help, see the glossary at the end of the lesson. INTRODUCTION TO THE FABACEAE The genus Phaseolus is part of the Fabaceae, or the Pea or Legume Family. This family is also known as the Leguminosae. TAXONOMISTS have different opinions on naming the family and how to treat the family. Members of the Fabaceae are HERBS, SHRUBS and TREES. Most of the members have alternate compound leaves. The FRUIT is usually a LEGUME, also called a pod. Members of the Fabaceae are often called LEGUMES. Legume crops like chickpeas, dry beans, dry peas, faba beans, lentils and lupine commonly have root nodules inhabited by beneficial bacteria called rhizobia. -
Biosystematic Studies in the Genus Piperia (Orchidaceae)
BIOSYSTEMATIC STUDIES IN THE GENUS PIPERIA (ORCHIDACEAE) by James D. Ackerman A Thesis Presented to The Faculty of Humboldt State University In Partial Fulfillment of the Requirements for the Degree Master of Arts June, 1976 BIOSYSTEMATIC STUDIES IN THE GENUS PIPERIA (ORCHIDACEAE) by James D. Ackerman Approved by the Master's Thesis Committee Chairman Approved by the Graduate Dean ACKNOWLEDGEMENTS Dennis E. Anderson's patience, guidance and support throughout this project is most gratefully acknowledged. I appreciate members of my committee, Richard L. Hurley, Robert A. Rasmussen, and Farris R. Meredith for lively discussions and reading the manuscript. I also thank William V. Allen for access to laboratory equipment, Jerry A. Powell for identifying the moths, Arlee M. Montalvo for aid through various aspects of this work, and the curators and staffs of those herbaria that provided specimens for study. TABLE OF CONTENTS Page Acknowledgements Introduction 1 Taxonomic History 7 Materials and Methods 12 Results and Discussion 22 Osmophors 22 Chromosomes 22 Chromatography 27 Interfertility 37 Field Studies 46 Morphology 49 Character analysis 49 Taxonomic concepts 60 Summary 66 Distribution 68 Conclusions 74 Taxonomy 79 Keys to Piperia taxa 79 Piperia 81 Piperia elegans 82 Piperia unalascensis 86 Piperia maritima 89 Piperia maritima var. multiflora 92 Piperia transversa 94 Piperia michaeli 96 iii Table of Contents. Continued. Page Appendices 98 Literature Cited 107 INTRODUCTION Piperia Rydberg is a polymorphic genus and presents complex taxonomic and nomenclatural problems. Variability exists in nearly all morphological aspects including the usually conservative features of the column. Many species have been proposed based on plants showing limited ranges of continuous characters; this has resulted in considerable confusion. -
Dermal Morphology of <Emphasis Type="Italic">Vanilla Planifolia
Proc. Indian Acad. Sci., Vol. 84 B, No. 5, 1976, pp. 173-179 Dermal morphology of Vanilla planifolia Andr. and V. wightii Lindl. B. K. NAYAR, F.A.Sc., RAJENDRA RAI AND P. VATSALA Department of Botany, Calicut University, Kerala 673635 MS received 8 April 1976 ABSTRACT In contrast to other Orchidaceae, the stomata in Va;ziila planifolia and V. wightii, are predominantly of the para-mesoperigenous type but the meristemoid is squarish as in other members of the family. 16~S of the stomata in V. planifclia and the stomata on the scale-leaves of V. wightii are of the aperigenous type; in V. planifolia, a few stomata (8~) are anisomesogenous (meristemoid triangular) and others (2~o) hemipara-mesop~rigenous. In V. Mghtii subsidiary cells of the para- mesoperigenous cauline stomata divide secondarily to form 5-7 subsidiary cells. Stomata are abundant on the stem of V. wightii (stomatal index-3.4) but sparse in V. planifolia (index-0.57). There is a progressive increase in stomatal index from base to apex of the leaf of V. planifolia. About 80~; of the the stomata in mature leaves of V. planifolia degenerate, as leaves get older.The epidermis is devoid of trichom~s in both species. In V. planifc.lia, each epidermal cell has a large crystal included in it. It is suggested that the stomatal types in Vanilla indicate the relationship of Orchidaceae to Hypoxidaceae, through Curculigo, which also has para- mesoperigenous stomata. 1. INTRODUCTION DIFFERENT Natural Orders, especially of the Monocotyledons, are reported to possess characteristic stomatal types and the aperigenous type is the rule in Orchidaceae. -
Guide to Theecological Systemsof Puerto Rico
United States Department of Agriculture Guide to the Forest Service Ecological Systems International Institute of Tropical Forestry of Puerto Rico General Technical Report IITF-GTR-35 June 2009 Gary L. Miller and Ariel E. Lugo The Forest Service of the U.S. Department of Agriculture is dedicated to the principle of multiple use management of the Nation’s forest resources for sustained yields of wood, water, forage, wildlife, and recreation. Through forestry research, cooperation with the States and private forest owners, and management of the National Forests and national grasslands, it strives—as directed by Congress—to provide increasingly greater service to a growing Nation. The U.S. Department of Agriculture (USDA) prohibits discrimination in all its programs and activities on the basis of race, color, national origin, age, disability, and where applicable sex, marital status, familial status, parental status, religion, sexual orientation genetic information, political beliefs, reprisal, or because all or part of an individual’s income is derived from any public assistance program. (Not all prohibited bases apply to all programs.) Persons with disabilities who require alternative means for communication of program information (Braille, large print, audiotape, etc.) should contact USDA’s TARGET Center at (202) 720-2600 (voice and TDD).To file a complaint of discrimination, write USDA, Director, Office of Civil Rights, 1400 Independence Avenue, S.W. Washington, DC 20250-9410 or call (800) 795-3272 (voice) or (202) 720-6382 (TDD). USDA is an equal opportunity provider and employer. Authors Gary L. Miller is a professor, University of North Carolina, Environmental Studies, One University Heights, Asheville, NC 28804-3299. -
Redalyc.A Study of the Dry Forest Communities in the Dominican
Anais da Academia Brasileira de Ciências ISSN: 0001-3765 [email protected] Academia Brasileira de Ciências Brasil GARCÍA-FUENTES, ANTONIO; TORRES-CORDERO, JUAN A.; RUIZ-VALENZUELA, LUIS; LENDÍNEZ-BARRIGA, MARÍA LUCÍA; QUESADA-RINCÓN, JUAN; VALLE- TENDERO, FRANCISCO; VELOZ, ALBERTO; LEÓN, YOLANDA M.; SALAZAR- MENDÍAS, CARLOS A study of the dry forest communities in the Dominican Republic Anais da Academia Brasileira de Ciências, vol. 87, núm. 1, marzo, 2015, pp. 249-274 Academia Brasileira de Ciências Rio de Janeiro, Brasil Available in: http://www.redalyc.org/articulo.oa?id=32738838023 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Anais da Academia Brasileira de Ciências (2015) 87(1): 249-274 (Annals of the Brazilian Academy of Sciences) Printed version ISSN 0001-3765 / Online version ISSN 1678-2690 http://dx.doi.org/10.1590/0001-3765201520130510 www.scielo.br/aabc A study of the dry forest communities in the Dominican Republic ANTONIO GARCÍA-FUENTES1, JUAN A. TORRES-CORDERO1, LUIS RUIZ-VALENZUELA1, MARÍA LUCÍA LENDÍNEZ-BARRIGA1, JUAN QUESADA-RINCÓN2, FRANCISCO VALLE-TENDERO3, ALBERTO VELOZ4, YOLANDA M. LEÓN5 and CARLOS SALAZAR-MENDÍAS1 1Departamento de Biología Animal, Biología Vegetal y Ecología, Facultad de Ciencias Experimentales, Universidad de Jaén, Campus Las Lagunillas, s/n, 23071 Jaén, España 2Departamento de Ciencias Ambientales, Facultad de Ciencias Ambientales y Bioquímica, Universidad de Castilla-La Mancha, Avda. Carlos III, s/n, 45071 Toledo, España 3Departamento de Botánica, Facultad de Ciencias, Universidad de Granada, Campus de Fuentenueva, Avda. -
Orchidaceae) from China
Phytotaxa 350 (3): 247–258 ISSN 1179-3155 (print edition) http://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2018 Magnolia Press Article ISSN 1179-3163 (online edition) https://doi.org/10.11646/phytotaxa.350.3.4 Two new natural hybrids in the genus Pleione (Orchidaceae) from China WEI ZHANG1, 2, 4, JIAO QIN1, 2, RUI YANG1, 2, 4, YI YANG3,4 & SHI-BAO ZHANG1, 2* 1Key Laboratory of Economic Plants and Biotechnology, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan, China. Email: [email protected] 2 Yunnan Key Laboratory for Wild Plant Resources, Kunming, Yunnan, China 3Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kun- ming, Yunnan, China 4 University of Chinese Academy of Sciences, Beijing, China Abstract Several species in the genus Pleione (Orchidaceae) have same or overlapping geographical distribution in China. In this study, two new natural hybrids, Pleione × baoshanensis and Pleione × maoershanensis, were described and illustrated. The parentage for these two hybrids was confirmed using molecular data from ITS of the nuclear ribosomal, trnT-trnL spacer and trnL-trnF region (trnL intron and trnL-trnF spacer) of the plastid DNA. Pleione × baoshanensis is intermediate between P. albiflora and P. yunnanensis, and characterized by its erose lamellae on the lip. Meanwhile, Pleione × maoershanensis is intermediate between P. hookeriana (P. chunii) and P. pleionoides, and characterized by its deep lacerate lamellae on the lip. For the individuals tested, molecular data suggest that P. albiflora is the maternal parent of Pleione × baoshanensis, and P. hookeriana (P. -
Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes
Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes Shichao Chen1., Dong-Kap Kim2., Mark W. Chase3, Joo-Hwan Kim4* 1 College of Life Science and Technology, Tongji University, Shanghai, China, 2 Division of Forest Resource Conservation, Korea National Arboretum, Pocheon, Gyeonggi- do, Korea, 3 Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, United Kingdom, 4 Department of Life Science, Gachon University, Seongnam, Gyeonggi-do, Korea Abstract Phylogenetic analysis aims to produce a bifurcating tree, which disregards conflicting signals and displays only those that are present in a large proportion of the data. However, any character (or tree) conflict in a dataset allows the exploration of support for various evolutionary hypotheses. Although data-display network approaches exist, biologists cannot easily and routinely use them to compute rooted phylogenetic networks on real datasets containing hundreds of taxa. Here, we constructed an original neighbour-net for a large dataset of Asparagales to highlight the aspects of the resulting network that will be important for interpreting phylogeny. The analyses were largely conducted with new data collected for the same loci as in previous studies, but from different species accessions and greater sampling in many cases than in published analyses. The network tree summarised the majority data pattern in the characters of plastid sequences before tree building, which largely confirmed the currently recognised phylogenetic relationships. Most conflicting signals are at the base of each group along the Asparagales backbone, which helps us to establish the expectancy and advance our understanding of some difficult taxa relationships and their phylogeny. -
Field Identification of the 50 Most Common Plant Families in Temperate Regions
Field identification of the 50 most common plant families in temperate regions (including agricultural, horticultural, and wild species) by Lena Struwe [email protected] © 2016, All rights reserved. Note: Listed characteristics are the most common characteristics; there might be exceptions in rare or tropical species. This compendium is available for free download without cost for non- commercial uses at http://www.rci.rutgers.edu/~struwe/. The author welcomes updates and corrections. 1 Overall phylogeny – living land plants Bryophytes Mosses, liverworts, hornworts Lycophytes Clubmosses, etc. Ferns and Fern Allies Ferns, horsetails, moonworts, etc. Gymnosperms Conifers, pines, cycads and cedars, etc. Magnoliids Monocots Fabids Ranunculales Rosids Malvids Caryophyllales Ericales Lamiids The treatment for flowering plants follows the APG IV (2016) Campanulids classification. Not all branches are shown. © Lena Struwe 2016, All rights reserved. 2 Included families (alphabetical list): Amaranthaceae Geraniaceae Amaryllidaceae Iridaceae Anacardiaceae Juglandaceae Apiaceae Juncaceae Apocynaceae Lamiaceae Araceae Lauraceae Araliaceae Liliaceae Asphodelaceae Magnoliaceae Asteraceae Malvaceae Betulaceae Moraceae Boraginaceae Myrtaceae Brassicaceae Oleaceae Bromeliaceae Orchidaceae Cactaceae Orobanchaceae Campanulaceae Pinaceae Caprifoliaceae Plantaginaceae Caryophyllaceae Poaceae Convolvulaceae Polygonaceae Cucurbitaceae Ranunculaceae Cupressaceae Rosaceae Cyperaceae Rubiaceae Equisetaceae Rutaceae Ericaceae Salicaceae Euphorbiaceae Scrophulariaceae