Eucalyptus Robusta Smith Myrtaceae Swamp Mahogany
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Two New Taxa of Verticordia (Myrtaceae: Chamelaucieae) from South-Western Australia
A.S.Nuytsia George 20: 309–318 & M.D. (2010)Barrett,, Two new taxa of Verticordia 309 Two new taxa of Verticordia (Myrtaceae: Chamelaucieae) from south-western Australia Alex S. George1 and Matthew D. Barrett2,3 1 ‘Four Gables’, 18 Barclay Road, Kardinya, Western Australia 6163 Email: [email protected] 2 Botanic Gardens and Parks Authority, Kings Park and Botanic Garden, Fraser Ave, West Perth, Western Australia 6005 3 School of Plant Biology, University of Western Australia, Crawley, Western Australia 6009 Email: [email protected] Abstract George, A.S. and Barrett, M.D. Two new taxa of Verticordia (Myrtaceae: Chamelaucieae) from south- western Australia. Nuytsia 20: 309–318 (2010). Verticordia mitchelliana subsp. implexior A.S.George & M.D.Barrett and Verticordia setacea A.S.George are described and discussed. Verticordia setacea belongs with V. gracilis A.S.George in section Platandra, previously a monotypic section. Introduction The genus Verticordia DC. (Myrtaceae: tribe Chamelaucieae) is a charismatic group of shrubs found mainly in south-western Australia, with several species in adjacent arid regions and three in tropical Australia (George 1991; George & Pieroni 2002). Verticordia is currently defined solely on the possession of divided calyx lobes, but the limits between Verticordia and the related genera Homoranthus A.Cunn. ex Schauer, Chamelaucium Desf. and Darwinia Rudge are difficult to define conclusively, and other characteristics such as anther morphology suggest conflicting relationships (Bentham 1867; Craven & Jones 1991; George 1991). A recent analysis using a single chloroplast gene, with limited sampling of Verticordia taxa (Ma et al. 2002), suggests that Verticordia may be polyphyletic. -
Eucalyptus Robusta NZ Myrtaceae Key - Online Edition Eucalyptus Robusta Sm
11/16/2020 Eucalyptus robusta NZ Myrtaceae Key - Online edition Eucalyptus robusta Sm. Common Names swamp mahogany, swamp messmate Origin Australia: coastal New South Wales to south-eastern Queensland. Cultivation In New Zealand predominantly cultivated for timber or amenity; very occasionally naturalised from nearby specimens. Distribution Mainly in northern coastal and lowland areas in the North Island of New Zealand. Distinguishing Features Tree with thick, fibrous, spongy, reddish-brown to grey-brown bark with deep longitudinal furrows, extending to the small branches. Mature leaves that are glossy, darker green on the upper side, paler beneath, strongly feather-veined. Long-stalked, spindle- or pear-shaped flower buds to 20 mm long and 9 mm wide, in clusters of 9–15. Fruit that are woody capsules, long-stalked, cylindrical to 18 mm long and 11 mm wide, with disc descending inside rim of capsule, and the three or four valve tips joined across the mouth of the capsule. Habit Tree to 30 m tall. Bark and Stem/Trunk Bark of main trunk thick, fibrous, spongy, reddish-brown to grey-brown, in elongated slabs with furrows between, extending to the small branches; ribbons absent. Hairs and adventitious roots absent. Young stems square in cross-section, sometimes winged. Leaves Mature leaves alternate, stalked, broadly lanceolate to ovate, feather-veined, tip pointed, base tapering to leaf stalk, glossy, dark green above and paler below, hairs absent, 85–170 mm long, 25–70 mm wide. Vein reticulation moderate to dense, main side-veins at a relatively wide angle to the midrib, intramarginal veins present just inside margin; oil glands usually inconspicuous; leaf stalk 15–30 mm long. -
Flying-Fox Dispersal Feasibility Study Cassia Wildlife Corridor, Coolum Beach and Tepequar Drive Roost, Maroochydore
Sunshine Coast Council Flying-Fox Dispersal Feasibility Study Cassia Wildlife Corridor, Coolum Beach and Tepequar Drive Roost, Maroochydore. Environmental Operations May 2013 0 | Page Table of Contents Introduction ................................................................................................................................ 2 Purpose ............................................................................................................................................... 2 Flying-fox Mitigation Strategies .......................................................................................................... 2 State and Federal Permits ................................................................................................................... 4 Roost Management Plan .................................................................................................................... 4 Risk ...................................................................................................................................................... 5 Flying-fox Dispersal Success in Australia ............................................................................................. 6 References .......................................................................................................................................... 7 Cassia Wildlife Corridor ................................................................................................................ 8 Background ........................................................................................................................................ -
Lauraceae Along an Altitudinal Gradient in Southern Brazil
Floresta e Ambiente 2019; 26(4): e20170637 https://doi.org/10.1590/2179-8087.063717 ISSN 2179-8087 (online) Original Article Forest Management Lauraceae Along an Altitudinal Gradient in Southern Brazil Marcelo Leandro Brotto1 , Eduardo Damasceno Lozano2 , Felipe Eduardo Cordeiro Marinero2 , Alexandre Uhlmann3 , Christopher Thomas Blum2 , Carlos Vellozo Roderjan2 1Prefeitura Municipal de Curitiba, Curitiba, PR, Brasil 2Universidade Federal do Paraná (UFPR), Curitiba, PR, Brasil 3Embrapa Pesca e Aquicultura, Palmas, TO, Brasil ABSTRACT We performed a phytosociological study on an altitudinal gradient in Lauráceas State Park (Parque Estadual das Lauráceas/PR), aiming to describe the Montane Atlantic Rain Forest, to verify the importance of Lauraceae, and to evaluate the communities’ successional stage. We distributed survey units (2,000 m² quadrats) along an altitudinal gradient and surveyed all individuals with DBH ≥ 10 cm, which composed the arboreal component. In smaller quadrats (250 m²), we surveyed regeneration individuals. The community at 800 and 900 m a.s.l. shows typical characteristics of Montane forest in an advanced successional stage, and the abundance of Ocotea catharinensis is its main indicator. At 1,000 and 1,100 m a.s.l., the forest is characterized as Montane with short stature in an advanced successional stage, with the occurrence of typical upper montane species such as O. porosa and O. vaccinioides. Keywords: Atlantic forest, Lauráceas State Park, phytosociology. Creative Commons License. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. 2/12 Brotto ML, Lozano ED, Marinero FEC, Uhlmann A, Blum CT, Roderjan CV Floresta e Ambiente 2019; 26(4): e20170637 1. -
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 -
Darwinia Hortiorum (Myrtaceae: Chamelaucieae), a New Species from the Darling Range, Western Australia
K.R.Nuytsia Thiele, 20: 277–281 Darwinia (2010) hortiorum (Myrtaceae: Chamelaucieae), a new species 277 Darwinia hortiorum (Myrtaceae: Chamelaucieae), a new species from the Darling Range, Western Australia Kevin R. Thiele Western Australian Herbarium, Department of Environment and Conservation, Locked Bag 104, Bentley Delivery Centre, Western Australia 6983 Email: [email protected] Abstract Thiele, K.R. Darwinia hortiorum (Myrtaceae: Chamelaucieae), a new species from the Darling Range, Western Australia. Nuytsia 20: 277–281 (2010). The distinctive, new, rare species Darwinia hortiorum is described, illustrated and discussed. Uniquely in the genus it has strongly curved- zygomorphic flowers with the sigmoid styles arranged so that they group towards the centre of the head-like inflorescences. Introduction Darwinia Rudge comprises c. 90 species, mostly from the south-west of Western Australia with c. 15 species in New South Wales, Victoria and South Australia. Phylogenetic analyses (M. Barrett, unpublished) have shown that the genus is polyphyletic, with distinct eastern and western Australian clades. Along with the related genera Actinodium Schauer, Chamelaucium Desf., Homoranthus A.Cunn. ex Schauer and Pileanthus Labill., the Darwinia clades are nested in a paraphyletic Verticordia DC. Many undescribed species of Darwinia are known in Western Australia, and these are being progressively described (Rye 1983; Marchant & Keighery 1980; Marchant 1984; Keighery & Marchant 2002; Keighery 2009). A significant number of taxa in the genus are narrowly endemic or rare and are of high conservation significance. Although taxonomic reassignment of the Western Australian species of Darwinia may be required in the future, resolving the status of these undescribed species and describing them under their current genus helps provide information for conservation assessments and survey. -
Flying Foxes Jerry Copy
Species Common Name Habit Flowering Fruit Notes Acacia macradenia Zigzag wattle Shrub August Possible pollen source Albizia lebbek Lebbek Tall tree summer Source of nectar. Excellent shade tree for large gardens. Alphitonia excelsa Red ash Tree October to March November to May Food source for Black and Grey- headed flying fox Angophora costata Smooth-barked Tall tree December to Source of nectar apple January Angophora Rough-barked apple Tall tree September to Source of nectar floribunda February Angophora costata Smooth-barked Tall tree November to Source of nectar subsp. leiocarpa apple, Rusty gum February Archontophoenix Alexander palm Tree-like November to January Food source for alexandrae December Spectacled flying fox. Good garden tree Archontophoenix Bangalow palm Tree-like February to June March to July Food source for cunninghamiana Grey-headed flying fox. Good garden tree Species Common Name Habit Flowering Fruit Notes Banksia integrifolia Coastal Shrub or small tree Recurrent, all year Food source for honeysuckle round Black and Grey- headed flying fox. Good garden tree Banksia serrata Old man banksia Shrub or small tree February to May Source of nectar. Good garden tree Buckinghamia Ivory curl tree Small tree December to Possible source of celsissima February nectar. Good garden tree Callistemon citrinus Crimson bottlebrush Shrub or small tree November and Source of nectar. March Good garden tree Callistemon salignus White bottlebrush Shrub or small tree spring Source of nectar. Good garden tree Castanospermum Moreton Bay Tall tree spring Source of nectar australe chestnut, Black bean Corymbia citriodora Lemon-scented gum Tall tree may flower in any Source of nectar season Corymbia Red bloodwood From mallee to tall summer to autumn Source of nectar gummifera tree Corymbia Pink bloodwood Tall tree December to March Source of nectar. -
Structures and Bioactive Properties of Myrtucommulones and Related Acylphloroglucinols from Myrtaceae
molecules Review Structures and Bioactive Properties of Myrtucommulones and Related Acylphloroglucinols from Myrtaceae Rosario Nicoletti 1,2 , Maria Michela Salvatore 3 , Pasquale Ferranti 2 and Anna Andolfi 3,* 1 Council for Agricultural Research and Economics, Research Centre for Olive, Citrus and Tree Fruit, 81100 Caserta, Italy; [email protected] 2 Department of Agriculture, University of Naples ‘Federico II’, 80055 Portici, Italy; [email protected] 3 Department of Chemical Sciences, University of Naples ‘Federico II’, 80126 Naples, Italy; [email protected] * Correspondence: andolfi@unina.it; Tel.: +39-081-2539179 Academic Editors: Francesco Vinale and Maria Luisa Balestrieri Received: 2 December 2018; Accepted: 17 December 2018; Published: 19 December 2018 Abstract: Myrtaceae are a group of plants that include a number of renowned species used in ethnomedicine in many areas worldwide. Their valuable therapeutic properties have stimulated a fruitful research activity addressed to the identification of the bioactive components of their extracts yielding a great diversity of terpenes; polyphenols; and other exclusive products. Among the latter, starting with the discovery of myrtucommulone A from myrtle (Myrtus communis), a series of structurally-related acylphloroglucinol compounds have been characterized from several species that represent the basic active principles to be considered in view of possible drug development. Aspects concerning chemical and biological properties of these products are reviewed in the present paper. Keywords: myrtucommulone; acylphloroglucinols; Myrtaceae; plant extracts; biological activities 1. Introduction Myrtle (Myrtus communis) is a typical shrub of maquis and coastal bushes native of the Mediterranean area and Western Asia. It is well-known in traditional medicine, and for centuries its leaves and berries have found ethnomedical application in the treatment of several disorders of the digestive apparatus, as well as pulmonary and skin diseases [1,2]. -
Morphology and Vascular Anatomy of the Flower of Angophora Intermedia
© Landesmuseum für Kärnten; download www.landesmuseum.ktn.gv.at/wulfenia; www.biologiezentrum.at Wulfenia 13 (2006): 11–19 Mitteilungen des Kärntner Botanikzentrums Klagenfurt Morphology and vascular anatomy of the fl ower of Angophora intermedia DC. (Myrtaceae) with special emphasis on the innervation of the fl oral axis Sergey A. Volgin & Anastasiya Stepanova Summary: A peculiar receptacle structure in Angophora intermedia DC. (Myrtaceae) has been determined by a vascular-anatomical method. The vascular system of the fl ower of A. intermedia consists of numerous ascending bundles and girdling bundles in the hypanthium and the inferior ovary wall. In the central column of the trilocular ovary we found a dense conical plexus of vascular bundles supplying the placentae (infralocular plexus). It is connected with ascending bundles of the receptacle in the ovary base. In its central part it contains “hanged” bundles and blind bundles, so it seems to be a residual stele of a rudimentary fl oral apex. Thus, the receptacle ofA. intermedia is toroidal at the level of fl oral organs and conical above the carpel node. Keywords: Angophora intermedia, Myrtaceae, fl ower morphology, vascular system, fl oral axis, innervation, anatomy The fl oral development in different species of Myrtaceae has been studied precisely to elucidate the homology of the inferior ovary, hypanthium, operculate perianth and stamens of the polymerous androecium (PAYER 1857; MAYR 1969; BUNNIGER 1972; DRINNAN & LADIGES 1988; RONSE DECRAENE & SMETS 1991; ORLOVICH et al. 1996). Developmental and histogenetical studies have shown, that the receptacle in the fl ower of Myrtaceae is cup-like and take part to certain extent in the formation of the inferior ovary wall and the hypanthium (PAYER 1857; BUNNIGER 1972; RONSE DECRAENE & SMETS 1991). -
Vascular Plant Families of the United States Grouped by Diagnostic Features
Humboldt State University Digital Commons @ Humboldt State University Botanical Studies Open Educational Resources and Data 12-6-2019 Vascular Plant Families of the United States Grouped by Diagnostic Features James P. Smith Jr Humboldt State University, [email protected] Follow this and additional works at: https://digitalcommons.humboldt.edu/botany_jps Part of the Botany Commons Recommended Citation Smith, James P. Jr, "Vascular Plant Families of the United States Grouped by Diagnostic Features" (2019). Botanical Studies. 96. https://digitalcommons.humboldt.edu/botany_jps/96 This Flora of the United States and North America is brought to you for free and open access by the Open Educational Resources and Data at Digital Commons @ Humboldt State University. It has been accepted for inclusion in Botanical Studies by an authorized administrator of Digital Commons @ Humboldt State University. For more information, please contact [email protected]. FLOWERING PLANT FAMILIES OF THE UNITED STATES GROUPED BY DIAGNOSTIC FEATURES James P. Smith, Jr. Professor Emeritus of Botany Department of Biological Sciences Humboldt State University Second edition — 6 December 2019 The focus is on families of plants found in the conterminous United States, including ornamentals. The listing of a family is not meant to imply that every species has that feature. I am using a fewfamily names, such as Liliaceae, Plantaginaceae, and Scrophulariaceae, in the traditional sense, because their limits remain unsettled. Parasitic on branches Dioscoreaceae -
Genera in Myrtaceae Family
Genera in Myrtaceae Family Genera in Myrtaceae Ref: http://data.kew.org/vpfg1992/vascplnt.html R. K. Brummitt 1992. Vascular Plant Families and Genera, Royal Botanic Gardens, Kew REF: Australian – APC http://www.anbg.gov.au/chah/apc/index.html & APNI http://www.anbg.gov.au/cgi-bin/apni Some of these genera are not native but naturalised Tasmanian taxa can be found at the Census: http://tmag.tas.gov.au/index.aspx?base=1273 Future reference: http://tmag.tas.gov.au/floratasmania [Myrtaceae is being edited at mo] Acca O.Berg Euryomyrtus Schaur Osbornia F.Muell. Accara Landrum Feijoa O.Berg Paragonis J.R.Wheeler & N.G.Marchant Acmena DC. [= Syzigium] Gomidesia O.Berg Paramyrciaria Kausel Acmenosperma Kausel [= Syzigium] Gossia N.Snow & Guymer Pericalymma (Endl.) Endl. Actinodium Schauer Heteropyxis Harv. Petraeomyrtus Craven Agonis (DC.) Sweet Hexachlamys O.Berg Phymatocarpus F.Muell. Allosyncarpia S.T.Blake Homalocalyx F.Muell. Pileanthus Labill. Amomyrtella Kausel Homalospermum Schauer Pilidiostigma Burret Amomyrtus (Burret) D.Legrand & Kausel [=Leptospermum] Piliocalyx Brongn. & Gris Angasomyrtus Trudgen & Keighery Homoranthus A.Cunn. ex Schauer Pimenta Lindl. Angophora Cav. Hottea Urb. Pleurocalyptus Brongn. & Gris Archirhodomyrtus (Nied.) Burret Hypocalymma (Endl.) Endl. Plinia L. Arillastrum Pancher ex Baill. Kania Schltr. Pseudanamomis Kausel Astartea DC. Kardomia Peter G. Wilson Psidium L. [naturalised] Asteromyrtus Schauer Kjellbergiodendron Burret Psiloxylon Thouars ex Tul. Austromyrtus (Nied.) Burret Kunzea Rchb. Purpureostemon Gugerli Babingtonia Lindl. Lamarchea Gaudich. Regelia Schauer Backhousia Hook. & Harv. Legrandia Kausel Rhodamnia Jack Baeckea L. Lenwebia N.Snow & ZGuymer Rhodomyrtus (DC.) Rchb. Balaustion Hook. Leptospermum J.R.Forst. & G.Forst. Rinzia Schauer Barongia Peter G.Wilson & B.Hyland Lindsayomyrtus B.Hyland & Steenis Ristantia Peter G.Wilson & J.T.Waterh. -
The Following Tree Seedlings Are Available to Order from the State of Hawaii Division of Forestry and Wildlife, State Tree Nursery
The following tree seedlings are available to order from the State of Hawaii Division of Forestry and Wildlife, State Tree Nursery: Scientific Name: Common Name: Dibble/ Pot size: Acacia koa……………………… Koa……………………………….. Small Acacia koaia……………………... Koai’a……………………………. Small Araucaria columnaris…………….. Norfolk-island Pine……………… Small Cryptomeria japonica……………. Sugi Pine………………………… Small Cupressus lusitanica……………... Mexican Cypress………………… Small Cupressus macrocarpa…………… Monterey Cypress……………….. Small Cupressus simpervirens………….. Italian Cypress…………………… Medium Eucalyptus deglupta……………… Rainbow Bark……………………. Small Eucalyptus robusta……………….. Swamp Mahogany……………….. Small Metrosideros polymorpha……….. Ohia……………………………… Medium or 3” pot Pinus elliotii……………………… Slash Pine………………………... Small Pinus radiata……………………... Monterey Pine…………………… Small Podocarpus sp……………………. Podocarpus………………………. 3” pot Santalum sp……………………… Sandalwood……………………… Medium or 3” pot Tristania conferta………………… Brush Box………………………... Small Acacia koa (Koa): This large hardwood tree is endemic to the Hawaiian Islands. The tree has exceeded 100 ft in height with basal diameter far beyond 50 inches in old growth stands. The wood is prized for furniture and canoe works. This legume has pods with black seeds for reproduction. The wood has similar properties to that of black walnut. The yellow flowers are borne in dense round heads about 2@ in diameter. Tree growth is best above 800 ft; seems to grow best in the ‘Koa belt’ which is situated at an elevation range between 3,500 - 6,000 ft. It is often found in areas where there is fog in the late afternoons. It should be planted in well- drained fertile soils. Grazing animals relish the Koa foliage, so young seedlings should be protected Acacia koaia (Koaia): Related to the Koa, Koaia is native to Hawaii. The leaves and flowers are much the same as Koa.