Floristic Survey Barachois De Mahebourg
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"National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary."
Intro 1996 National List of Vascular Plant Species That Occur in Wetlands The Fish and Wildlife Service has prepared a National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary (1996 National List). The 1996 National List is a draft revision of the National List of Plant Species That Occur in Wetlands: 1988 National Summary (Reed 1988) (1988 National List). The 1996 National List is provided to encourage additional public review and comments on the draft regional wetland indicator assignments. The 1996 National List reflects a significant amount of new information that has become available since 1988 on the wetland affinity of vascular plants. This new information has resulted from the extensive use of the 1988 National List in the field by individuals involved in wetland and other resource inventories, wetland identification and delineation, and wetland research. Interim Regional Interagency Review Panel (Regional Panel) changes in indicator status as well as additions and deletions to the 1988 National List were documented in Regional supplements. The National List was originally developed as an appendix to the Classification of Wetlands and Deepwater Habitats of the United States (Cowardin et al.1979) to aid in the consistent application of this classification system for wetlands in the field.. The 1996 National List also was developed to aid in determining the presence of hydrophytic vegetation in the Clean Water Act Section 404 wetland regulatory program and in the implementation of the swampbuster provisions of the Food Security Act. While not required by law or regulation, the Fish and Wildlife Service is making the 1996 National List available for review and comment. -
Notes on Two Newly Naturalized Plants in Taiwan
Taiwania, 53(2): 230-235, 2008 Notes on Two Newly Naturalized Plants in Taiwan Ming-Jer Jung(1), Tien-Chuan Hsu(2) and Shih-Wen Chung(3,4) (Manuscript received 17 December, 2007; accepted 20 March, 2008) ABSTRACT: Hypochaeris glabra L. (Asteraceae) was recently collected in central Taiwan, and Kyllinga polyphylla Willd. ex Kunth. (Cyperaceae) was found in northern Taiwan. Both two species were considered as naturalized plants to the flora of Taiwan. Herein, the authors provide line drawings, distribution maps and descriptions of these two alien plants. KEY WORDS: Asteraceae, Cyperaceae, flora, Hypochaeris glabra, Kyllinga polyphylla, Taiwan. INTRODUCTION 1. Hypochaeris glabra L. Sp. Pl. 2: 811. 1753. Barkley et al., 2006. Asteraceae. In: Baillargeon Two alien plants were considered as naturalized G. et al. (eds.), Flora of North America 19: in Taiwan, and were described in this article. 297-299; DeFilipps R. A., 1976. In: Tutin, T. G. Hypochaeris glabra L. (Asteraceae) was found in et al. (eds.), Flora Europaea 3: 308-309; Koyama, central Taiwan (Fig. 1) and considered as naturalized H., 1995. In: Iwatsuki, K. et al. (eds.), Flora of by the authors. Many naturalized members of Japan III b: 2-3. 光貓兒菊 Figs. 1 & 2 Asteraceae in Taiwan were reported in recent (Chang et al., 2002; Chen, 2007; Chung et al., 2007; Hsu et Herb, annual or perennial, taproot one or roots al., 2006; Jung et al., 2005, 2006; Wang and Chen, several, stems erect, basal leaves oblanceolate, 2006; Yang and Hsieh, 2006). Nearly half of toothed, glabrous to hispidulate, hispid 0.3-0.5 mm naturalized species of Asteraceae were considered as long. -
Sour Paspalum
Sour Paspalum - Tropical Weed or Forage? ALAN A. BEETLE Bissinda (Gabon), bitter grass (Philippines), camalote de antena (Mexico), canamazo (Cuba), cafiamazo hembro (Cuba), Highlight: Where carpetgraSs (Axonopus compressus) will cafiamazo amargo (Cuba), capim amargoso (Brazil), capim grow, sour paspalum (Paspalum conjugatum) has no place and marreca (Brazil), capim papuao (Brazil), carabao grass (Phil- is probably a sign of poor management. However, in areas of ippines), cintillo (Peru), co dang (Indochina), calapi (Philip- poor or sour soils, in shade and in times of drought, sour pas- pines), djuba-gov6 (Gabon), &inga (Gabon), gamalote (Costa palum comes into its own throughout the tropics as a valuable Rica), ge’singa (Gabon), gisinga (Gabon), grama de antena component of the total forage resource. Paspalum is a rather large genus “numbering nearly 400” species (Chase, 1929). Sour paspalum (Paspalum conjugatum) stands by itself in this genus as suggested by Chase (1929) who created for it, alone, the Section Conjugata (Fig. 1). Its most unusual character is the vigorously stoloniferous habit allowing, at times, for a rapidly formed perennial ground cover. Sour paspalum has been assumed to be native where it occurs in the Americas, from Florida to Texas and southward to Peru, Bolivia, and northern Argentina, from sea level to 4,000 ft elevation. The grass was first described from a specimen collected in Surinam (Dutch Guiana). Sour paspalum has been assumed, however, to be intro- duced wherever it occurs in the Old World tropics (Fig. 2) and Pacific Islands. The early trade routes were between Australia, Singapore, and Africa. Probably both carpetgrass (Axonopus compressus) and sour paspalum, being of similar distribution and ecology, were spread at the same time to the same places. -
Appendix Color Plates of Solanales Species
Appendix Color Plates of Solanales Species The first half of the color plates (Plates 1–8) shows a selection of phytochemically prominent solanaceous species, the second half (Plates 9–16) a selection of convol- vulaceous counterparts. The scientific name of the species in bold (for authorities see text and tables) may be followed (in brackets) by a frequently used though invalid synonym and/or a common name if existent. The next information refers to the habitus, origin/natural distribution, and – if applicable – cultivation. If more than one photograph is shown for a certain species there will be explanations for each of them. Finally, section numbers of the phytochemical Chapters 3–8 are given, where the respective species are discussed. The individually combined occurrence of sec- ondary metabolites from different structural classes characterizes every species. However, it has to be remembered that a small number of citations does not neces- sarily indicate a poorer secondary metabolism in a respective species compared with others; this may just be due to less studies being carried out. Solanaceae Plate 1a Anthocercis littorea (yellow tailflower): erect or rarely sprawling shrub (to 3 m); W- and SW-Australia; Sects. 3.1 / 3.4 Plate 1b, c Atropa belladonna (deadly nightshade): erect herbaceous perennial plant (to 1.5 m); Europe to central Asia (naturalized: N-USA; cultivated as a medicinal plant); b fruiting twig; c flowers, unripe (green) and ripe (black) berries; Sects. 3.1 / 3.3.2 / 3.4 / 3.5 / 6.5.2 / 7.5.1 / 7.7.2 / 7.7.4.3 Plate 1d Brugmansia versicolor (angel’s trumpet): shrub or small tree (to 5 m); tropical parts of Ecuador west of the Andes (cultivated as an ornamental in tropical and subtropical regions); Sect. -
Grass Genera in Townsville
Grass Genera in Townsville Nanette B. Hooker Photographs by Chris Gardiner SCHOOL OF MARINE and TROPICAL BIOLOGY JAMES COOK UNIVERSITY TOWNSVILLE QUEENSLAND James Cook University 2012 GRASSES OF THE TOWNSVILLE AREA Welcome to the grasses of the Townsville area. The genera covered in this treatment are those found in the lowland areas around Townsville as far north as Bluewater, south to Alligator Creek and west to the base of Hervey’s Range. Most of these genera will also be found in neighbouring areas although some genera not included may occur in specific habitats. The aim of this book is to provide a description of the grass genera as well as a list of species. The grasses belong to a very widespread and large family called the Poaceae. The original family name Gramineae is used in some publications, in Australia the preferred family name is Poaceae. It is one of the largest flowering plant families of the world, comprising more than 700 genera, and more than 10,000 species. In Australia there are over 1300 species including non-native grasses. In the Townsville area there are more than 220 grass species. The grasses have highly modified flowers arranged in a variety of ways. Because they are highly modified and specialized, there are also many new terms used to describe the various features. Hence there is a lot of terminology that chiefly applies to grasses, but some terms are used also in the sedge family. The basic unit of the grass inflorescence (The flowering part) is the spikelet. The spikelet consists of 1-2 basal glumes (bracts at the base) that subtend 1-many florets or flowers. -
Appendix 9.2 Plant Species Recorded Within the Assessment Area
Appendix 9.2: Plant Species Recorded within the Assessment Area Agricultural Area Storm Water Fishponds Mudflat / Native/ Developed Distribution in Protection Village / Drain / Natural Modified and Coastal Scientific Name Growth Form Exotic to Area / Plantation Grassland Shrubland Woodland Marsh Mangrove Hong Kong (1) Status Orchard Recreational Watercourse Watercourse Mitigation Water Hong Kong Wasteland Dry Wet Pond Ponds Body Abrus precatorius climber: vine native common - + subshrubby Abutilon indicum native restricted - ++ herb Acacia auriculiformis tree exotic - - ++++ +++ + ++++ ++ +++ Acacia confusa tree exotic - - ++++ + +++ ++ ++ ++++ ++ ++++ Acanthus ilicifolius shrub native common - + ++++ Acronychia pedunculata tree native very common - ++ Adenosma glutinosum herb native very common - + + Adiantum capillus-veneris herb native common - + ++ ++ Adiantum flabellulatum herb native very common - + +++ +++ shrub or small Aegiceras corniculatum native common - +++ tree Aeschynomene indica shrubby herb native very common - + Ageratum conyzoides herb exotic common - ++ ++ ++ ++ ++ + Ageratum houstonianum herb exotic common - ++ + Aglaia odorata shrub exotic common - +++ + +++ + Aglaonema spp. herb - - - + + rare (listed under Forests and Ailanthus fordii (3) small tree native + Countryside Ordinance Cap. 96) Alangium chinense tree or shrub native common - ++ + ++ + +++ + Albizia lebbeck tree exotic - - +++ Alchornea trewioides shrub native common - + Aleurites moluccana tree exotic common - +++ ++ ++ ++ Allamanda cathartica climbing -
Flora of China 22: 604–605. 2006. 201. DICHANTHIUM Willemet, Ann
Flora of China 22: 604–605. 2006. 201. DICHANTHIUM Willemet, Ann. Bot. (Usteri) 18: 11. 1796. 双花草属 shuang hua cao shu Chen Shouliang (陈守良); Sylvia M. Phillips Eremopogon Stapf; Lepeocercis Trinius. Perennial, rarely annual. Leaf blades often cauline, linear; ligule membranous. Inflorescence of single or subdigitate racemes, terminal or also axillary and sometimes supported by spathes; racemes usually with 1 or more basal homogamous spikelet pairs, spikelets often imbricate; rachis internodes and pedicels slender, solid, bearded, truncate or oblique at apex. Sessile spikelet dorsally compressed; callus short, obtuse; lower glume papery to cartilaginous, broadly convex to slightly concave, sometimes pitted, rounded on flanks, becoming 2-keeled upward, apex obtuse; upper glume boat-shaped, dorsally keeled, awnless; lower floret reduced to an empty hyaline lemma; upper lemma stipitiform, entire, awned from apex; awn geniculate, glabrous or puberulous. Stamens (2–) 3. Pedicelled spikelet similar to the sessile, male or barren, awnless. About 20 species: Africa through India to SE Asia and Australia; three species in China. Dichanthium is closely related to Bothriochloa, but can be distinguished by its pedicels and rachis internodes being solid and lacking a median, purple line. The species present in China are not clear-cut and are also variable within themselves due to polyploidy and apomixis. All three species provide good grazing and now occur widely in tropical regions as introductions or escapes. 1a. Peduncle pilose below inflorescence ........................................................................................................................... 1. D. aristatum 1b. Peduncle glabrous. 2a. Lower glume of sessile spikelet obovate, winged along keels; leaf sheaths compressed; ligule less than 1 mm, margin ciliate ........................................................................................................................................................ 2. D. caricosum 2b. -
24. Tribe PANICEAE 黍族 Shu Zu Chen Shouliang (陈守良); Sylvia M
POACEAE 499 hairs, midvein scabrous, apex obtuse, clearly demarcated from mm wide, glabrous, margins spiny-scabrous or loosely ciliate awn; awn 1–1.5 cm; lemma 0.5–1 mm. Anthers ca. 0.3 mm. near base; ligule ca. 0.5 mm. Inflorescence up to 20 cm; spike- Caryopsis terete, narrowly ellipsoid, 1–1.8 mm. lets usually densely arranged, ascending or horizontally spread- ing; rachis scabrous. Spikelets 1.5–2.5 mm (excluding awns); Stream banks, roadsides, other weedy places, on sandy soil. Guangdong, Hainan, Shandong, Taiwan, Yunnan [Bhutan, Cambodia, basal callus 0.1–0.2 mm, obtuse; glumes narrowly lanceolate, India, Indonesia, Laos, Malaysia, Myanmar, Nepal, Philippines, Sri back scaberulous-hirtellous in rather indistinct close rows (most Lanka, Thailand, Vietnam; Africa (probably introduced), Australia obvious toward lemma base), midvein pectinate-ciliolate, apex (Queensland)]. abruptly acute, clearly demarcated from awn; awn 0.5–1.5 cm. Anthers ca. 0.3 mm. Caryopsis terete, narrowly ellipsoid, ca. 3. Perotis hordeiformis Nees in Hooker & Arnott, Bot. Beech- 1.5 mm. Fl. and fr. summer and autumn. 2n = 40. ey Voy. 248. 1838. Sandy places, along seashores. Guangdong, Hebei, Jiangsu, 麦穗茅根 mai sui mao gen Yunnan [India, Indonesia, Malaysia, Nepal, Myanmar, Pakistan, Sri Lanka, Thailand]. Perotis chinensis Gandoger. This species is very close to Perotis indica and is sometimes in- Annual or short-lived perennial. Culms loosely tufted, cluded within it. No single character by itself is reliable for separating erect or decumbent at base, 25–40 cm tall. Leaf sheaths gla- the two, but the combination of characters given in the key will usually brous; leaf blades lanceolate to narrowly ovate, 2–4 cm, 4–7 suffice. -
19. KYLLINGA Rottbøll, Descr. Icon. Rar. Pl. 12. 1773, Nom. Cons., Not Killinga Adanson (1763)
Fl. China 23: 246–249. 2010. 19. KYLLINGA Rottbøll, Descr. Icon. Rar. Pl. 12. 1773, nom. cons., not Killinga Adanson (1763). 水蜈蚣属 shui wu gong shu Dai Lunkai (戴伦凯); Gordon C. Tucker, David A. Simpson Herbs, perennial or rarely annual, with rhizomes or only fibrous roots. Culms tufted or scattered, usually slightly slender, rarely slightly stout. Leaves basal, 3-ranked; ligule absent; leaf blade elongated or reduced. Involucral bracts spreading, leaflike. Inflores- cences terminal, capitate, with 1–3 spikes. Spikes sessile, capitate, with densely numerous spikelets. Spikelets short, compressed, each usually with 1 or 2(–5) bisexual flowers; rachilla articulate near base, deciduous at articulation when mature. Glumes disti- chous, persistent on rachilla and deciduous with it, basal 2 without a flower, apicalmost rarely with a male flower, remaining ones each with a bisexual flower. Flowers without perianth bristles or scalelike perianth parts. Style base not swollen, deciduous; stigmas 2. Nutlet compressed biconvex, one angle toward rachilla. About 75 species: tropics and warm temperate regions worldwide; seven species (one introduced) in China. 1a. Glumes abaxially keeled. 2a. Perennials, with rhizomes; glumes with membranous spiny denticulate wings ................................................. 6. K. nemoralis 2b. Annuals, with fibrous roots; glumes with papery broadly dentate wings shaped like a cockscomb ................ 7. K. squamulata 1b. Glumes not abaxially keeled. 3a. Rhizomes short; culms tufted; spikes (1–)3; glume abaxial keel without spinules. 4a. Middle spike broadly ovoid, 5–6 mm; lateral spikes globose, 3–4 mm; spikelets oblong, 1-flowered; glumes greenish yellow and reddish brown maculate ....................................................................................... 1. K. bulbosa 4b. Middle spike oblong-cylindric to oblong, 6–14 mm; lateral spikes oblong, ca. -
University of California Santa Cruz Responding to An
UNIVERSITY OF CALIFORNIA SANTA CRUZ RESPONDING TO AN EMERGENT PLANT PEST-PATHOGEN COMPLEX ACROSS SOCIAL-ECOLOGICAL SCALES A dissertation submitted in partial satisfaction of the requirements for the degree of DOCTOR OF PHILOSOPHY in ENVIRONMENTAL STUDIES with an emphasis in ECOLOGY AND EVOLUTIONARY BIOLOGY by Shannon Colleen Lynch December 2020 The Dissertation of Shannon Colleen Lynch is approved: Professor Gregory S. Gilbert, chair Professor Stacy M. Philpott Professor Andrew Szasz Professor Ingrid M. Parker Quentin Williams Acting Vice Provost and Dean of Graduate Studies Copyright © by Shannon Colleen Lynch 2020 TABLE OF CONTENTS List of Tables iv List of Figures vii Abstract x Dedication xiii Acknowledgements xiv Chapter 1 – Introduction 1 References 10 Chapter 2 – Host Evolutionary Relationships Explain 12 Tree Mortality Caused by a Generalist Pest– Pathogen Complex References 38 Chapter 3 – Microbiome Variation Across a 66 Phylogeographic Range of Tree Hosts Affected by an Emergent Pest–Pathogen Complex References 110 Chapter 4 – On Collaborative Governance: Building Consensus on 180 Priorities to Manage Invasive Species Through Collective Action References 243 iii LIST OF TABLES Chapter 2 Table I Insect vectors and corresponding fungal pathogens causing 47 Fusarium dieback on tree hosts in California, Israel, and South Africa. Table II Phylogenetic signal for each host type measured by D statistic. 48 Table SI Native range and infested distribution of tree and shrub FD- 49 ISHB host species. Chapter 3 Table I Study site attributes. 124 Table II Mean and median richness of microbiota in wood samples 128 collected from FD-ISHB host trees. Table III Fungal endophyte-Fusarium in vitro interaction outcomes. -
Plant Species List for Bob Janes Preserve
Plant Species List for Bob Janes Preserve Scientific and Common names obtained from Wunderlin 2013 Scientific Name Common Name Status EPPC FDA IRC FNAI Family: Azollaceae (mosquito fern) Azolla caroliniana mosquito fern native R Family: Blechnaceae (mid-sorus fern) Blechnum serrulatum swamp fern native Woodwardia virginica Virginia chain fern native R Family: Dennstaedtiaceae (cuplet fern) Pteridium aquilinum braken fern native Family: Nephrolepidaceae (sword fern) Nephrolepis cordifolia tuberous sword fern exotic II Nephrolepis exaltata wild Boston fern native Family: Ophioglossaceae (adder's-tongue) Ophioglossum palmatum hand fern native E I G4/S2 Family: Osmundaceae (royal fern) Osmunda cinnamomea cinnamon fern native CE R Osmunda regalis royal fern native CE R Family: Polypodiaceae (polypody) Campyloneurum phyllitidis long strap fern native Phlebodium aureum golden polypody native Pleopeltis polypodioides resurrection fern native Family: Psilotaceae (whisk-fern) Psilotum nudum whisk-fern native Family: Pteridaceae (brake fern) Acrostichum danaeifolium giant leather fern native Pteris vittata China ladder break exotic II Family: Salviniaceae (floating fern) Salvinia minima water spangles exotic I Family: Schizaeaceae (curly-grass) Lygodium japonicum Japanese climbing fern exotic I Lygodium microphyllum small-leaf climbing fern exotic I Family: Thelypteridaceae (marsh fern) Thelypteris interrupta hottentot fern native Thelypteris kunthii widespread maiden fern native Thelypteris palustris var. pubescens marsh fern native R Family: Vittariaceae -
Senna Obtusifolia (L.) Irwin & Barneby
Crop Protection Compendium - Senna obtusifolia (L.) Irwin & Barneby Updated by Pierre Binggeli 2005 NAMES AND TAXONOMY Preferred scientific name Senna obtusifolia (L.) Irwin & Barneby Taxonomic position Other scientific names Domain: Eukaryota Cassia obtusifolia L. Kingdom: Viridiplantae Cassia tora var. obtusifolia (L.) Haines Phylum: Spermatophyta Emelista tora (L.) Britton & Rosa Subphylum: Angiospermae Cassia tora L. Class: Dicotyledonae Senna tora (L.) Roxb. Order: Myrtales Family: Fabaceae BAYER code Subfamily: Caesalpinioideae CASOB (Cassia obtusifolia) Common names English: bicho Mauritius: sicklepod chilinchil cassepuante Cuba: herbe pistache Australia: guanina Pacific Islands: Java bean Dominican Republic: peanut weed Bolivia: brusca cimarrona Paraguay: aya-poroto brusca hembra taperva moroti mamuri El Salvador: taperva Brazil: comida de murcielago taperva sayju fedegoso frijolillo Puerto Rico: fedegoso-branco Guatemala: dormidera mata pasto ejote de invierno Venezuela: matapasto liso ejotil chiquichique Colombia: Madagascar: bichomacho voamahatsara Notes on taxonomy and nomenclature Many recent floras use the new nomenclature which puts many former Cassia spp. including C. obtusifolia and C. tora, into the genus Senna, and the new classification of Irwin and Barneby (1982) is used here. However, where acknowledging these two species as separate (following Irwin and Barneby 1982), in terms of their agronomic importance and control, there is probably little difference between S. obtusifolia and S. tora, and both are included together for the purpose of this datasheet. Thus, whereas S. tora (and C. tora) are included here as non-preferred scientific names, they are not strictly synonyms. Binggeli updated 2005 Crop Protection Compendium - Senna obtusifolia (L.) Irwin & Barneby 1 There has been much debate on the classification of S. obtusifolia.