THE Why and HOW of Plant Names
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02. CENTAUREA.Indd
ActaCentaurea Botanica sect. MalacitanaCyanus en la 35. Península 23-55 Ibérica Málaga, 201023 REVISIÓN TAXONÓMICA DEL COMPLEJO DE CENTAUREA CYANUS L. (CENTAUREA SECT. CYANUS, ASTERACEAE) EN LA PENÍNSULA IBÉRICA Adolfo Francisco MUÑOZ1 y Juan Antonio DEVESA2* Dirección de los autores.1Departamento de Biología Ambiental y Salud Pública, Facultad de Ciencias Experimentales, Universidad de Huelva, Avenida de la Fuerzas Armadas s/n, 21071-Badajoz, España 2Departamento de Botánica, Ecología y Fisiología Vegetal, Facultad de Ciencias, Universidad de Córdoba, Campus de Rabanales, Edificio José Celestino Mutis, ctra. de Madrid km. 396, 14071-Córdoba, y Jardín Botánico de Córdoba, Avda. de Linneo s/n, 14004-Córdoba, España. *Autor para correspondencia: [email protected] Recibido el 1 de septiembre de 2010, aceptado para su publicación el 10 de octubre de 2010 RESUMEN. Revisión taxonómica del complejo de Centaurea cyanus L. (Centaurea sect. Cyanus, Asteraceae) en la Península Ibérica. Se ha efectuado la revisión taxonómica de Centaurea sect. Cyanus en la Península Ibérica. Se reconocen seis táxones y se hacen dos nuevas combinaciones: C. triumfettii var. semidecurrens (Jord.) Muñoz Rodr. & Devesa y C. graminifolia (Lam.) Muñoz Rodr. & Devesa. Se aporta una clave para la identificación de los táxones, así como su descripción morfológica e información sobre la distribución geográfica, apetencias ecológicas, fenología y número cromosómico. Palabras clave. Asteraceae, Centaurea, corología, taxonomía, Península Ibérica. ABSTRACT. Taxonomic revision of the Centaurea cyanus L. complex (Centaurea sect. Cyanus, Asteraceae) in the Iberian Peninsula. A taxonomic review of Centaurea sect. Cyanus in the Iberian Peninsula was done. Six taxa are recognized and two new combinations are proposed: C. triumfetti var. -
Autumn Willow in Rocky Mountain Region the Black Hills National
United States Department of Agriculture Conservation Assessment Forest Service for the Autumn Willow in Rocky Mountain Region the Black Hills National Black Hills National Forest, South Dakota and Forest Custer, South Dakota Wyoming April 2003 J.Hope Hornbeck, Carolyn Hull Sieg, and Deanna J. Reyher Species Assessment of Autumn willow in the Black Hills National Forest, South Dakota and Wyoming J. Hope Hornbeck, Carolyn Hull Sieg and Deanna J. Reyher J. Hope Hornbeck is a Botanist with the Black Hills National Forest in Custer, South Dakota. She completed a B.S. in Environmental Biology (botany emphasis) at The University of Montana and a M.S. in Plant Biology (plant community ecology emphasis) at the University of Minnesota-Twin Cities. Carolyn Hull Sieg is a Research Plant Ecologist with the Rocky Mountain Research Station in Flagstaff, Arizona. She completed a B.S. in Wildlife Biology and M.S. in Range Science from Colorado State University and a Ph.D. in Range and Wildlife Management (fire ecology) at Texas Tech University. Deanna J. Reyher is Ecologist/Soil Scientist with the Black Hills National Forest in Custer, South Dakota. She completed a B.S. degree in Agronomy (soil science and crop production emphasis) from the University of Nebraska – Lincoln. EXECUTIVE SUMMARY Autumn willow, Salix serissima (Bailey) Fern., is an obligate wetland shrub that occurs in fens and bogs in the northeastern United States and eastern Canada. Disjunct populations of autumn willow occur in the Black Hills of South Dakota. Only two populations occur on Black Hills National Forest lands: a large population at McIntosh Fen and a small population on Middle Boxelder Creek. -
Blanket Flower, Gaillardia Spp
A Horticulture Information article from the Wisconsin Master Gardener website, posted 2 Feb 2015 Blanket Flower, Gaillardia spp. With brightly colored daisy-like fl owers in shades of red, orange, and yellow, the heat-tolerant and heavy blooming blanket fl ower is a good addition to the informal garden. There are about 25-30 species of Gaillardia, a genus of annuals, biennials, and perennials in the sunfl ower family (Asteraceae) all native to the Americas. The common name blanket fl ower may have come from the resemblance of the fl owers to brightly patterned Native American blankets in similar colors, the ability of wild species to completely cover the ground with a blanket of color, or even to the legend of a Native American weaver whose grave was always covered with blooming fl owers that were as brilliantly colored as the blankets he had made. The genus was named after French naturalist Antoine Rene Gaillard de Charentoneau. The fi rst species described in 1788 was Blanket fl ower has brightly colored the annual G. pulchella (= G. drummondi, G. bicolor), native from red and/or yellow fl owers. the southeastern US through to Colorado and south into Mexico, with its 2-inch fl owers of red with yellow tips. Lewis and Clark collected the much larger- fl owered, short-lived perennial G. aristata in Montana in 1806, with its variable fringed fl owers in reds and yellows. These two species hybridized in a Belgian garden in 1857 to produce Gaillardia x grandifl ora, the most common type of blanket fl ower grown in gardens. -
Djvu Document
BULL. BOT. SURV. INDIA Vol. 40. Nos. 1-4 : pp. 34-46/ 1998 COMPARATIVE MORPHO-ANATOMICAL STUDY OF CYPSELAS IN SOME SPECIES OF THE TRIBE I-IELIANTHEAE (ASTERACEAE) SOBHANKR. MUKHERJEE AND A. K. SARKAR Department of Bgrany, University of Kalyani, Kalyani, W.B. ABSTRACT A comparative study of morphology and anatomy of mature cypselas in 14 species belonging to 10 genera, such as BIDENS,CHRYSANTHELLUM, COREOPSIS, COSMOS,ECHINACEA, GAILLARDIA, GLOSSOGYNE, HBLIANTHUS, TITHONIA and XANTHIUM under the tribe Heliantheae (Asteraceae) was undertaken under light and scanning electron microscopes. Morphologically the form and structure of cypselas, carpopodia and pappus are diacritical for characterization of taxa. In all species pericarp is well differentiated into 2 zones. Cells of the epicarp are usually tangentially elongated, provided with yellow or brown substances. Mesocarp is mainly differentiated into 4 zones. Number and distribution of vascular traces, phytomelan layer and secretory cavities are taxonomically significant in certain taxa. An artificial bxonomic key using the detailed morphological, anatomical arid 'SEM ob'servations An the mature cypselas are provided. Key Words :Asteraceae-Heliantheae-Morphology-Anatomy of cypselas. INTRODUCTION for the tribe Heliantheae have been studied by The tribe Heliantheae is considered as one several workers like ~isra(1973), Pandey of the most primitive and largest tribes of the (1976,1977), Saenz (1981), Robinson (1981), family Asteraceae by Cronquist (1955). The Stuessy and Liu (1983), Randey et al. (1986), tribe Peliantheae has been included in the and Karis (1993a, 1993b). The present study is subfamily ksteroideae by Brerner (1996). to supplement these observations. According to Karis (1993 b), the Heliantheae MAmRIALS AND METHODS (s. -
Flowering Plants of South Norwood Country Park
Flowering Plants Of South Norwood Country Park Robert Spencer Introduction South Norwood Country Park relative to its size contains a wide range habitats and as a result a diverse range of plants can be found growing on site. Some of these plants are very conspicuous, growing in great abundance and filling the park with splashes of bright colour with a white period in early May largely as a result of the Cow Parsley, this is followed later in the year by a pink period consisting of mainly Willow herbs. Other plants to be observed are common easily recognisable flowers. However there are a great number of plants growing at South Norwood Country Park that are less well-known or harder to spot, and the casual observer would likely be surprised to learn that 363 species of flowering plants have so far been recorded growing in the park though this number includes invasive species and garden escapes. This report is an update of a report made in 2006, and though the site has changed in the intervening years the management and fundamental nature of the park remains the same. Some plants have diminished and some have flourished and the high level of diversity is still present. Many of these plants are important to other wildlife particularly in their relationship to invertebrate pollinators, and some of these important interactions are referenced in this report. With so many species on the plant list there is a restriction on how much information is given for each species, with some particularly rare or previously observed but now absent plants not included though they appear in the index at the back of the report including when they were last observed. -
List of Plants for Great Sand Dunes National Park and Preserve
Great Sand Dunes National Park and Preserve Plant Checklist DRAFT as of 29 November 2005 FERNS AND FERN ALLIES Equisetaceae (Horsetail Family) Vascular Plant Equisetales Equisetaceae Equisetum arvense Present in Park Rare Native Field horsetail Vascular Plant Equisetales Equisetaceae Equisetum laevigatum Present in Park Unknown Native Scouring-rush Polypodiaceae (Fern Family) Vascular Plant Polypodiales Dryopteridaceae Cystopteris fragilis Present in Park Uncommon Native Brittle bladderfern Vascular Plant Polypodiales Dryopteridaceae Woodsia oregana Present in Park Uncommon Native Oregon woodsia Pteridaceae (Maidenhair Fern Family) Vascular Plant Polypodiales Pteridaceae Argyrochosma fendleri Present in Park Unknown Native Zigzag fern Vascular Plant Polypodiales Pteridaceae Cheilanthes feei Present in Park Uncommon Native Slender lip fern Vascular Plant Polypodiales Pteridaceae Cryptogramma acrostichoides Present in Park Unknown Native American rockbrake Selaginellaceae (Spikemoss Family) Vascular Plant Selaginellales Selaginellaceae Selaginella densa Present in Park Rare Native Lesser spikemoss Vascular Plant Selaginellales Selaginellaceae Selaginella weatherbiana Present in Park Unknown Native Weatherby's clubmoss CONIFERS Cupressaceae (Cypress family) Vascular Plant Pinales Cupressaceae Juniperus scopulorum Present in Park Unknown Native Rocky Mountain juniper Pinaceae (Pine Family) Vascular Plant Pinales Pinaceae Abies concolor var. concolor Present in Park Rare Native White fir Vascular Plant Pinales Pinaceae Abies lasiocarpa Present -
Ecology of a Fire-Dependent Moth, Schinia Masoni, and Its Host Plant in Colorado
Ecology of a Fire-Dependent Moth, Schinia masoni, and its Host Plant in Colorado Bruce A. Byers,# Laurie S. Huckaby,§ and Merrill R. Kaufmann § © Unpublished Manuscript 2004 # To whom correspondence should be addressed; 405 Timber Lane Falls Church, VA 22046 USA Tel: (703) 534-4436 Email: [email protected] § U.S. Forest Service, Rocky Mountain Research Station 240 West Prospect Fort Collins, CO 80526 Running head: Ecology of the Colorado Firemoth Ecology of the Colorado Firemoth – Byers, Huckaby, and Kaufmann 2004 – page 2 ABSTRACT Schinia masoni is a generally rare noctuid moth, endemic to the northern Front Range of Colorado. Its larvae feed on the developing seeds of its host plant Gaillardia aristata, blanketflower. The objectives of this study were to investigate the possible fire-dependence of G. aristata , and to quantify the relationship between time since a fire and the abundance of G. aristata and S. masoni. The abundance of blanketflower and S. masoni larvae were recorded in four burned areas and in adjacent unburned areas in 2002, and at six additional sites in 2003, representing a range of one to approximately 100 years since a fire. Blanketflower populations increase dramatically at most sites within one year after a fire. Schinia masoni can be common in dense, post-fire blanketflower populations. Blanketflower abundance declines over time, and this species becomes uncommon in areas that have not burned in decades. Schinia masoni may persist as a fire-dependent metapopulation, colonizing newly-burned “islands” with abundant blanketflowers, and becoming locally extinct where its host plant has declined to low levels in unburned forests. -
Working List of Invasive Vascular Plants of Wyoming ─ III (Vernacular Names from Selected Major Works) Dec 2017
Working List of Invasive Vascular Plants of Wyoming ─ III (Vernacular names from selected major works) Dec 2017 Compiled by R.L. Hartman and B.E. Nelson With assistance from R.D. Dorn, W. Fertig, B. Heidel The following list contains 372 taxa introduced to Wyoming from outside North America; included are invasives recognized by the Wyoming state government as noxious (; 28; although Ambrosa tomentosa is native). A number of these species repesent escapes from cultivation and are limited to one or a few collections. Nomenclature is based on R.D. Dorn, 2001, Vascular Plants of Wyoming; where updated, Dorn’s synonyms are in square brackets [ ]. Other synonyms found in the list of sources below are not included. Likewise, family names and their circumscriptions follow Dorn; where defined differently by the Angiosperm Working Group IV (APG IV), clarification follows in parenthese. Dorn does not indicate the typical variety or subspecies unless a second infraspecific taxon is recognized. We have included the typical infraspecies where appropriate. The lack of hyphenation, word separation, or capitalization may not reflect the appearance of the vernacular names in the works cited. Sources for vernacular names: 1 Weed Science Society of America. 2010. Composite List of Weeds. 2 Kartesz, J.T., The Biota of North America Program (BONAP). 2015. Taxonomic Data Center. 3 P. Rice. 2000. Invaders Database System. Univ. of Montana. Release 14 Feb 2000 (not available for update). 4 Flora of the Great Plains Association. 1986. Flora of the Great Plains. Univ. Oklahoma Press. 5 C.L. Hitchcock & A. Cronquist. 2018. Flora of the Pacific Northwest. -
Gardens and Stewardship
GARDENS AND STEWARDSHIP Thaddeus Zagorski (Bachelor of Theology; Diploma of Education; Certificate 111 in Amenity Horticulture; Graduate Diploma in Environmental Studies with Honours) Submitted in fulfilment of the requirements for the degree of Doctor of Philosophy October 2007 School of Geography and Environmental Studies University of Tasmania STATEMENT OF AUTHENTICITY This thesis contains no material which has been accepted for any other degree or graduate diploma by the University of Tasmania or in any other tertiary institution and, to the best of my knowledge and belief, this thesis contains no copy or paraphrase of material previously published or written by other persons, except where due acknowledgement is made in the text of the thesis or in footnotes. Thaddeus Zagorski University of Tasmania Date: This thesis may be made available for loan or limited copying in accordance with the Australian Copyright Act of 1968. Thaddeus Zagorski University of Tasmania Date: ACKNOWLEDGEMENTS This thesis is not merely the achievement of a personal goal, but a culmination of a journey that started many, many years ago. As culmination it is also an impetus to continue to that journey. In achieving this personal goal many people, supervisors, friends, family and University colleagues have been instrumental in contributing to the final product. The initial motivation and inspiration for me to start this study was given by Professor Jamie Kirkpatrick, Dr. Elaine Stratford, and my friend Alison Howman. For that challenge I thank you. I am deeply indebted to my three supervisors Professor Jamie Kirkpatrick, Dr. Elaine Stratford and Dr. Aidan Davison. Each in their individual, concerted and special way guided me to this omega point. -
Blanketflower (Gaillardia Aristata) Plant Guide
Plant Guide from, arist, Latin for bristle, in reference to the hairy BLANKETFLOWER stems and leaves, and the awn-like bristles on the single-seeded fruit (achene). The blanketflower Gaillardia aristata Pursh inflorescence is said to resemble the colorful, Plant Symbol = GAAR intricate patterns woven into blankets made by Native Americans (Kimball and Lesica, 2005). Contributed by: USDA NRCS Bridger Plant Blanketflower is found in grasslands, woodlands, and Materials Center, Montana montane meadows. Its natural range extends from southern Canada on both sides of the Rocky Mountains, south to Utah, Colorado, and South Dakota (Strickler, 1993). Taxonomy: Blanketflower is tap rooted, with one or commonly several, erect stems from the base (Hitchcock et al., 1955). The pubescent plant grows to a height of 26 inches with rough-hairy, lance- shaped, alternate leaves, 6 inches long, 1 inch wide, entire to coarsely-toothed, or rarely pinnately divided (Hermann, 1966). The flower heads are radiate, showy, solitary to few, with an outer series of ray flowers and an inner group of disk flowers. There are typically 13, sterile, 0.6 to 1.4 inches long, ligulate Gaillardia aristata Susan R. Winslow, Bridger Plant Materials (strap-shaped), yellow ray flowers with purple bases Center (eFloras, 2011). The number and shape of the ray flowers is variable, as is the number of lobes in a ray Alternate Names (Robbins, 1908). A normal flower head has a large Indian blanketflower, common gaillardia, gaillardia, number of ligulate and tubular-shaped rays, with the brown-eyed Susan latter shape being four-lobed. A few flower heads have all tubular rays. -
Guidebook to Invasive Nonnative Plants of the Elwha Watershed Restoration
Guidebook to Invasive Nonnative Plants of the Elwha Watershed Restoration Olympic National Park, Washington Cynthia Lee Riskin A project submitted in partial fulfillment of the requirements for the degree of Master of Environmental Horticulture University of Washington 2013 Committee: Linda Chalker-Scott Kern Ewing Sarah Reichard Joshua Chenoweth Program Authorized to Offer Degree: School of Environmental and Forest Sciences Guidebook to Invasive Nonnative Plants of the Elwha Watershed Restoration Olympic National Park, Washington Cynthia Lee Riskin Master of Environmental Horticulture candidate School of Environmental and Forest Sciences University of Washington, Seattle September 3, 2013 Contents Figures ................................................................................................................................................................. ii Tables ................................................................................................................................................................. vi Acknowledgements ....................................................................................................................................... vii Introduction ....................................................................................................................................................... 1 Bromus tectorum L. (BROTEC) ..................................................................................................................... 19 Cirsium arvense (L.) Scop. (CIRARV) -
Phylogenetic Relationships of Plasmopara, Bremia and Other
Mycol. Res. 108 (9): 1011–1024 (September 2004). f The British Mycological Society 1011 DOI: 10.1017/S0953756204000954 Printed in the United Kingdom. Phylogenetic relationships of Plasmopara, Bremia and other genera of downy mildew pathogens with pyriform haustoria based on Bayesian analysis of partial LSU rDNA sequence data Hermann VOGLMAYR1, Alexandra RIETHMU¨LLER2, Markus GO¨KER3, Michael WEISS3 and Franz OBERWINKLER3 1 Institut fu¨r Botanik und Botanischer Garten, Universita¨t Wien, Rennweg 14, A-1030 Wien, Austria. 2 Fachgebiet O¨kologie, Fachbereich Naturwissenschaften, Universita¨t Kassel, Heinrich-Plett-Strasse 40, D-34132 Kassel, Germany. 3 Lehrstuhl fu¨r Spezielle Botanik und Mykologie, Botanisches Institut, Universita¨tTu¨bingen, Auf der Morgenstelle 1, D-72076 Tu¨bingen, Germany. E-mail : [email protected] Received 28 December 2003; accepted 1 July 2004. Bayesian and maximum parsimony phylogenetic analyses of 92 collections of the genera Basidiophora, Bremia, Paraperonospora, Phytophthora and Plasmopara were performed using nuclear large subunit ribosomal DNA sequences containing the D1 and D2 regions. In the Bayesian tree, two main clades were apparent: one clade containing Plasmopara pygmaea s. lat., Pl. sphaerosperma, Basidiophora, Bremia and Paraperonospora, and a clade containing all other Plasmopara species. Plasmopara is shown to be polyphyletic, and Pl. sphaerosperma is transferred to a new genus, Protobremia, for which also the oospore characteristics are described. Within the core Plasmopara clade, all collections originating from the same host family except from Asteraceae and Geraniaceae formed monophyletic clades; however, higher-level phylogenetic relationships lack significant branch support. A sister group relationship of Pl. sphaerosperma with Bremia lactucae is highly supported.