Albizia Lebbeck (L.) Benth
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Mealy Bugs Attack on Rain Tree
MEALY BUGS ATTACK ON RAIN TREE Geography of Mumbai city The Deccan region of India, the capital city of Maharashtra and economical capital of country, Mumbai lies on the western coast of India by the bank of Arabian Sea. Mumbai is made from the group of seven islands and is thus called as the Island city. It covers the total area of 603 sq. km. Most of this largest city of India is at sea level and the average altitude ranges from 10-15 metres from MSL. It has a hilly northern part and the highest point of Mumbai is at 450 metres in Sanjay Gandhi National Park. The eastern coast of Island has rows of mangroves, wherein the western coast happens to be sandy and stony. Due to proximity to the sea, the soil cover of this region is sandy to large extent. The rocks of this area are made up of Black Deccan Basalt pours, its acid and some basic variables. This island city of Mumbai is divided into two main regions, the city and the suburbs. These suburbs have alluvial soil type. Climate of Mumbai The Climate of Mumbai is a tropical wet and dry climate. Mumbai's climate can be best described as moderately hot with high degree of humidity. Its coastal nature and tropical location ensures temperatures won't fluctuate much throughout the year. The mean average is 27.2 °C and average rainfall is 242.2 cm (95.35 inches).[1] The mean maximum average temperatures in about 32 °C (90 °F) in summer and 30 °C (86 °F) in winter, while the average minimums are 25 °C (77 °F) in summer and 20.5 °C (68.9 °F) in winter. -
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 -
Evaluation of Wood Properties from Six Native Species of Forest Plantations in Costa Rica
BOSQUE 37(1): 71-84, 2016 DOI: 10.4067/S0717-92002016000100008 Evaluation of wood properties from six native species of forest plantations in Costa Rica Estudio de propiedades de la madera de seis especies nativas en plantaciones de Costa Rica Carolina Tenorio a, Róger Moya a*, Cynthia Salas a, Alexander Berrocal a * Corresponding author: a Instituto Tecnológico de Costa Rica, Escuela de Ingeniería Forestal, Apartado 159-7050, CIIBI-ITCR, Cartago, Costa Rica, [email protected] SUMMARY This study details information about physical, chemical and mechanical properties, drying, preservation and workability of wood from Cordia alliodora, Dipteryx panamensis, Enterolobium cyclocarpum, Hieronyma alchorneoides, Samanea saman and Vochysia ferruginea trees, growing in forest plantations in Costa Rica. Variation of the general properties in relation to height showed that heartwood percentage decreases, bark percentage increases and pith percentage is not affected. Dipteryx panamensis showed both the highest values for specific gravity and the highest mechanic resistance. Both chemical properties and extractives presence were different among species. Heartwood was not possible to preserve in any of the species, though sapwood was. Penetration varied from partial irregular or vascular in the species. The highest durability was for Hieronyma alchorneoides and Vochysia ferruginea, species classified as of high durability. Finally, all species had good performance in the workability tests. The previous results indicate that these species, used for trading reforestation in Costa Rica, have acceptable characteristics to be commercialized and used in wooden products. Key words: tropical species, Central America, wood variation, commercial wood. RESUMEN El presente estudio detalla información de las propiedades físicas, químicas, mecánicas, de secado, preservación y trabajabilidad de la madera de Cordia alliodora, Dipteryx panamensis, Enterolobium cyclocarpum, Hieronyma alchorneoides, Samanea saman y Vochysia ferruginea proveniente de plantaciones forestales en Costa Rica. -
Vegetation Mapping of the Mariana Islands: Commonwealth of the Northern Mariana Islands and Territory of Guam
VEGETATION MAPPING OF THE MARIANA ISLANDS: COMMONWEALTH OF THE NORTHERN MARIANA ISLANDS AND TERRITORY OF GUAM NOVEMBER 2017 FINAL REPORT FRED AMIDON, MARK METEVIER1 , AND STEPHEN E. MILLER PACIFIC ISLAND FISH AND WILDLIFE OFFICE, U.S. FISH AND WILDLIFE SERVICE, HONOLULU, HI 1 CURRENT AGENCY: BUREAU OF LAND MANAGEMENT, MEDFORD, OR Photograph of Alamagan by Curt Kessler, USFWS. Mariana Island Vegetation Mapping Final Report November 2017 CONTENTS List of Figures ............................................................................................................................................................................ 3 List of Tables .............................................................................................................................................................................. 4 Abbreviations ............................................................................................................................................................................ 5 Summary ..................................................................................................................................................................................... 6 Introduction ............................................................................................................................................................................... 7 Description of Project Area ........................................................................................................................................... -
Mimosa (Albizia Julibrissin)
W232 Mimosa (Albizia julibrissin) Becky Koepke-Hill, Extension Assistant, Plant Sciences Greg Armel, Assistant Professor, Extension Weed Specialist for Invasive Weeds, Plant Sciences Origin: Mimosa is native to Asia, from Iran to Japan. It was introduced to the United States in 1745 as an ornamental plant. Description: Mimosa is a legume with double-compound leaves that give the 20- to 40-foot tree a fern-like appear- ance. Each leaf has 10 to 25 leaflets and 40 to 60 subleaflets per leaflet. In the summer, the tree pro- duces pink puff flowers. Fruits are produced in the fall and are contained in tan seedpods. The tree often has multiple stems and a broad, spreading canopy. Seed- lings can be confused with other double-compound legumes, but mimosa does not have thorns or prickles like black locust (Robinia pseudoacacia), and has a woody base, unlike hemp sesbania (Sesbania exaltata). Habitat: Mimosa is cold-hardy to USDA hardiness zone 6 and is not found in elevations above 3,000 feet. Mimosa will thrive in full sun in a wide range of soils in any dis- turbed habitat, such as stream banks, roadsides and old fields. Mimosa can live in partial shade, but is almost never found in full shade or dense forests. Mi- mosa often spreads by seeds from nearby ornamental plantings, or by fill dirt containing mimosa seeds. It is a growing problem in aquatic environments, where mimosa gets started on the disturbed stream banks, and its seeds are carried by the running water. Environmental Impact: Mimosa is challenging to remove once it is estab- lished. -
Albizia Zygia Fabaceae
Albizia zygia (DC.) Macbr. Fabaceae - Mimosoideae LOCAL NAMES Igbo (nyie avu); Swahili (nongo); Yoruba (ayin rela) BOTANIC DESCRIPTION Albizia zygia is a deciduous tree 9-30 m tall with a spreading crown and a graceful architectural form. Bole tall and clear, 240 cm in diameter. Bark grey and smooth. Young branchlets densely to very sparsely clothed with minute crisped puberulence, usually soon disappearing but sometimes persistent. Leaves pinnate, pinnae in 2-3 pairs and broadening towards the apex, obliquely rhombic or obovate with the distal pair largest, apex obtuse, 29- 72 by 16-43 mm, leaves are glabrous or nearly so. Flowers subsessile; pedicels and calyx puberulous, white or pink; staminal tube exserted for 10-18 mm beyond corolla. Fruit pod oblong, flat or somewhat transversely plicate, reddish-brown in colour, 10-18 cm by 2-4 cm glabrous or nearly so. The seeds of A. zygia are smaller (7.5-10 mm long and 6.5 to 8.5 mm wide) and flatter than either of the other Albizia, but have the characteristic round shape, with a slightly swollen center. The genus was named after Filippo del Albizzi, a Florentine nobleman who in 1749 introduced A. julibrissin into cultivation. BIOLOGY A hermaphroditic species flowering in January, February, March, August, and September. Fruits ripen in January, February, March, April, November, and December. This tree hybridizes with A. gummifera. Agroforestry Database 4.0 (Orwa et al.2009) Page 1 of 5 Albizia zygia (DC.) Macbr. Fabaceae - Mimosoideae ECOLOGY A light demanding pioneer species, it is rarely found in closed canopy forests dominated by Chlorophora regia and Ficus macrosperma. -
Germination and Salinity Tolerance of Seeds of Sixteen Fabaceae Species in Thailand for Reclamation of Salt-Affected Lands
BIODIVERSITAS ISSN: 1412-033X Volume 21, Number 5, May 2020 E-ISSN: 2085-4722 Pages: 2188-2200 DOI: 10.13057/biodiv/d210547 Germination and salinity tolerance of seeds of sixteen Fabaceae species in Thailand for reclamation of salt-affected lands YONGKRIAT KU-OR1, NISA LEKSUNGNOEN1,2,♥, DAMRONGVUDHI ONWIMON3, PEERAPAT DOOMNIL1 1Department of Forest Biology, Faculty of Forestry, Kasetsart University. 50 Phahonyothin Rd, Lat yao, Chatuchak, Bangkok 10900, Thailand 2Center for Advanced Studies in Tropical Natural Resources, National Research University, Kasetsart University. 50 Phahonyothin Rd, Lat yao, Chatuchak, Bangkok 10900, Thailand. ♥email: [email protected] 3Department of Agronomy, Faculty of Agriculture, Kasetsart University. 50 Phahonyothin Rd, Lat Yao, Chatuchak, Bangkok 10900, Thailand. Manuscript received: 26 March 2020. Revision accepted: 24 April 2020. Abstract. Ku-Or Y, Leksungnoen N, Onwinom D, Doomnil P. 2020. Germination and salinity tolerance of seeds of sixteen Fabaceae species in Thailand for reclamation of salt-affected lands. Biodiversitas 21: 2188-2200. Over the years, areas affected by salinity have increased dramatically in Thailand, resulting in an urgent need for reclamation of salt-affected areas using salinity tolerant plant species. In this context, seed germination is an important process in plant reproduction and dispersion. This research aimed to study the ability of 16 fabaceous species to germinate and tolerate salt concentrations of at 6 different levels (concentration of sodium chloride solution, i.e., 0, 8, 16, 24, 32, and 40 dS m-1). The germination test was conducted daily for 30 days, and parameters such as germination percentage, germination speed, and germination synchrony were calculated. The electrical conductivity (EC50) was used to compare the salt-tolerant ability among the 16 species. -
Northern Cape Provincial Gazette Vol 15 No
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Exempted Trees List
Prohibited Plants List The following plants should not be planted within the City of North Miami. They do not require a Tree Removal Permit to remove. City of North Miami, 2017 Comprehensive List of Exempted Species Pg. 1/4 Scientific Name Common Name Abrus precatorius Rosary pea Acacia auriculiformis Earleaf acacia Adenanthera pavonina Red beadtree, red sandalwood Aibezzia lebbek woman's tongue Albizia lebbeck Woman's tongue, lebbeck tree, siris tree Antigonon leptopus Coral vine, queen's jewels Araucaria heterophylla Norfolk Island pine Ardisia crenata Scratchthroat, coral ardisia Ardisia elliptica Shoebutton, shoebutton ardisia Bauhinia purpurea orchid tree; Butterfly Tree; Mountain Ebony Bauhinia variegate orchid tree; Mountain Ebony; Buddhist Bauhinia Bischofia javanica bishop wood Brassia actino-phylla schefflera Calophyllum antillanum =C inophyllum Casuarina equisetifolia Australian pine Casuarina spp. Australian pine, sheoak, beefwood Catharanthus roseus Madagascar periwinkle, Rose Periwinkle; Old Maid; Cape Periwinkle Cestrum diurnum Dayflowering jessamine, day blooming jasmine, day jessamine Cinnamomum camphora Camphortree, camphor tree Colubrina asiatica Asian nakedwood, leatherleaf, latherleaf Cupaniopsis anacardioides Carrotwood Dalbergia sissoo Indian rosewood, sissoo Dioscorea alata White yam, winged yam Pg. 2/4 Comprehensive List of Exempted Species Scientific Name Common Name Dioscorea bulbifera Air potato, bitter yam, potato vine Eichhornia crassipes Common water-hyacinth, water-hyacinth Epipremnum pinnatum pothos; Taro -
Albizia Julibrissin Durazz
Albizia julibrissin Durazz. Fabaceae - Mimosoideae LOCAL NAMES Chinese (ho hun,ho huan); Dutch (acacia van Constantinopel); English (pink siris,Persian acacia,pink silk tree,mimosa,silk mimosa tree,silk tree,silky acacia,pink mimosa); French (arbre à soie,acacie de Constantinople); German (persische Seidenakazie,Julibrissin- Albizzie); Hindi (karmaru,brind,lal,tandai,shishi,sirin,siris,kurmru); Italian (acacia di Constantinopoli,gaggia di Constaninopoli,gaggia arborea,albero de la seta); Japanese (nemu-no-ki); Nepali (kato siris) BOTANIC DESCRIPTION Bark (James H. Miller, USDA Forest Albizia julibrissin is a small to medium-sized tree 6-9 m tall with a Service, www.forestryimages.org) spreading crown. The bark is light brown, nearly smooth, and generally thin with lens shaped areas along the stem. Leaves large, up to 50 cm long, bipinnately compound with 10-35 pairs of leaflets, many oblong leaflets, each only 6-12 mm long by about 7.5-10 cm wide, and alternate along the stems. Leaves fold up under the night sky Flowers showy, fragrant pink, about 3.75 cm long, that resembling pompoms and are arranged in panicles at the ends of branches. Fruits are flat, straw-colored pods about 15 cm long containing light brown Quick growing, flat-topped crown. Branches oval-shaped seeds about 1.25 cm in length. in lateral tiers. Long feathery fern-like leaves up to 45cm long - provide light shade. Spectacular in flower - from early summer to The generic name commemorates the Florentine nobleman Filippo degli autumn. Ornamental used as avenue tree Albizzi, who introduced the plant into cultivation in the middle of the 18th and lawn shade. -
Albizia Lophantha (Willd.) Benth, PLUME ALBIZIA, PLUME ACACIA
Albizia lophantha (Willd.) Benth, PLUME ALBIZIA, PLUME ACACIA. Small tree, evergreen, unarmed, 1-trunked, in range to 8 m tall; main branches horizontal, with widely spaced leaves; trunk < 12 cm diameter; bark fibrous and tough, grayish brown, brownish below wax, dull, transversely wrinkled, weakly ridged with smooth longitudinally veins and finer wrinkles. Stems: ridged, somewhat zigzagged, streaked olive green and rosy brown and becoming dark purple on ridges, internodes mostly 50–70 mm long, canescent. Leaves: helically alternate, even-2-pinnately compound with 7–13(–15) pairs of primary leaflets, petiolate, with stipules; stipules 2, attached to stem, acuminate and scalelike, hairy, persistent; petiole typically 30–60 mm long, with a conspicuous pulvinus at base and an extrafloral nectary at midpoint, the nectary oval, ± 3 mm long, green; blade oblong to chevron-rectangular in outline, 180–210 × 110–140 mm, with primary leaflets spreading or ascending, spaced 9−14 mm apart along rachis; rachis strongly ridged, with canescent hairs and erect, reddish glandular hairs, primary leaflets lacking stipel and having an extrafloral nectary at junction of the terminal pair of primary leaflets and sometimes another nectary at junction of penultimate pair of primary leaflets; petiolules with conspicuous pulvinus, having an upper pair of minute appendages at tip; primary leaflets often diverging at about 30−60°, 50–120 mm long, symmetric in length but lower leaflet length < terminal < middle leaflet length, with 25–40 pairs of secondary leaflets along axis; secondary leaflets with sleep movements, overlapping, asymmetrically oblong to elliptic, 3.5–8 × 1–2 mm, oblique at base, entire, broadly acute at tip, pinnately veined, upper surface glabrous, lower surface strigose and glaucous. -
Albizia Chevalieri, And
学位論文 Studies on bioactive compounds from Cameroonian medicinal plants, Acacia albida and Albizia chevalieri, and Japanese endophytes Xylaria sp. (カメルーン産薬用植物 Acacia albida と Albizia chevalieri と日本で分離された植物内生菌類 Xylaria sp.の生理活性物質に関する研究) Abdou Tchoukoua Dedication To My late mom DJEBBA M. Odile i Acknowledgments Acknowledgments This thesis was successful with the support of a number of people to whom I am greatly indebted. I would like to express my sincere gratitude to my supervisors, Prof. Dr. Yoshihito Shiono (Yamagata University, Japan) and Prof. Ngadjui T. Bonaventure (University of Yaounde I, Cameroon) for the guidance, support, and motivation during all the time of my research in their labs. Their help will always be deeply appreciated. I would also like to thank the JSPS-Ronpaku Program for financial support in Japan. I wish to express my gratitude to Prof. M. Hashimoto, Prof. Y. Tokuji, Prof. K. Kimura, and Prof. T. Koseki, for their participation as judging committee. I wish to thank all the people with whom I have worked and contributed to the development of this work. Great thanks to Prof. Dr. Özgen Çaliskan for my sojourn in her lab, and to Dr. Ibrahim Horo in offering his expertise in isolation of saponins. I wish to thank Prof. K. Kimura for analyses of biological activities. I thank Drs Eunsang Kwon and Hiroyuki Momma for measurements of ESI-MS spectra. I am particularly grateful to Dr. T. Tabopda for his contribution to the success of this investigation. It has been a pleasure working with you. I thank the staff members of the Department of Organic Chemistry of the University of Yaounde I for my university education.