South Pasadena Tree Guide
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The Native Vegetation of the Nattai and Bargo Reserves
The Native Vegetation of the Nattai and Bargo Reserves Project funded under the Central Directorate Parks and Wildlife Division Biodiversity Data Priorities Program Conservation Assessment and Data Unit Conservation Programs and Planning Branch, Metropolitan Environmental Protection and Regulation Division Department of Environment and Conservation ACKNOWLEDGMENTS CADU (Central) Manager Special thanks to: Julie Ravallion Nattai NP Area staff for providing general assistance as well as their knowledge of the CADU (Central) Bioregional Data Group area, especially: Raf Pedroza and Adrian Coordinator Johnstone. Daniel Connolly Citation CADU (Central) Flora Project Officer DEC (2004) The Native Vegetation of the Nattai Nathan Kearnes and Bargo Reserves. Unpublished Report. Department of Environment and Conservation, CADU (Central) GIS, Data Management and Hurstville. Database Coordinator This report was funded by the Central Peter Ewin Directorate Parks and Wildlife Division, Biodiversity Survey Priorities Program. Logistics and Survey Planning All photographs are held by DEC. To obtain a Nathan Kearnes copy please contact the Bioregional Data Group Coordinator, DEC Hurstville Field Surveyors David Thomas Cover Photos Teresa James Nathan Kearnes Feature Photo (Daniel Connolly) Daniel Connolly White-striped Freetail-bat (Michael Todd), Rock Peter Ewin Plate-Heath Mallee (DEC) Black Crevice-skink (David O’Connor) Aerial Photo Interpretation Tall Moist Blue Gum Forest (DEC) Ian Roberts (Nattai and Bargo, this report; Rainforest (DEC) Woronora, 2003; Western Sydney, 1999) Short-beaked Echidna (D. O’Connor) Bob Wilson (Warragamba, 2003) Grey Gum (Daniel Connolly) Pintech (Pty Ltd) Red-crowned Toadlet (Dave Hunter) Data Analysis ISBN 07313 6851 7 Nathan Kearnes Daniel Connolly Report Writing and Map Production Nathan Kearnes Daniel Connolly EXECUTIVE SUMMARY This report describes the distribution and composition of the native vegetation within and immediately surrounding Nattai National Park, Nattai State Conservation Area and Bargo State Conservation Area. -
Vegetation on Fraser Island
Vegetation On Fraser Island Imagine towering pines, rainforest trees with three metre girths, rare and ancient giant ferns, eucalypt forests with their characteristic pendulous leaves, lemon-scented swamp vegetation and dwarfed heathland shrubs covered in a profusion of flowers. Now imagine them all growing on an island of sand. Two of Fraser Island’s unique features are its diversity of vegetation and its ability to sustain this vegetation in sand, a soil that is notoriously low in nutrients essential to plant growth. Plants growing on the dunes can obtain their nutrients (other than nitrogen) from only two sources - rain and sand. Sand is coated with mineral compounds such as iron and aluminium oxides. Near the shore the air contains nutrients from sea spray which are deposited on the sand. In a symbiotic relationship, fungi in the sand make these nutrients available to the plants. These in turn supply various organic compounds to the fungi which, having no chlorophyll cannot synthesise for themselves. Colonising plants, such as spinifex, grow in this nutrient poor soil and play an integral role in the development of nutrients in the sand. Once these early colonisers have added much needed nutrients to the soil, successive plant communities that are also adapted to low nutrient conditions, can establish themselves. She-oaks ( Allocasuarina and Casuarina spp.) can be found on the sand dunes of the eastern beach facing the wind and salt spray. These hardy trees are a familiar sight throughout the island with their thin, drooping branchlets and hard, woody cones. She-oaks are known as nitrogen fixers and add precious nutrients to the soil. -
Checklist of Illinois Native Trees
Technical Forestry Bulletin · NRES-102 Checklist of Illinois Native Trees Jay C. Hayek, Extension Forestry Specialist Department of Natural Resources & Environmental Sciences Updated May 2019 This Technical Forestry Bulletin serves as a checklist of Tree species prevalence (Table 2), or commonness, and Illinois native trees, both angiosperms (hardwoods) and gym- county distribution generally follows Iverson et al. (1989) and nosperms (conifers). Nearly every species listed in the fol- Mohlenbrock (2002). Additional sources of data with respect lowing tables† attains tree-sized stature, which is generally to species prevalence and county distribution include Mohlen- defined as having a(i) single stem with a trunk diameter brock and Ladd (1978), INHS (2011), and USDA’s The Plant Da- greater than or equal to 3 inches, measured at 4.5 feet above tabase (2012). ground level, (ii) well-defined crown of foliage, and(iii) total vertical height greater than or equal to 13 feet (Little 1979). Table 2. Species prevalence (Source: Iverson et al. 1989). Based on currently accepted nomenclature and excluding most minor varieties and all nothospecies, or hybrids, there Common — widely distributed with high abundance. are approximately 184± known native trees and tree-sized Occasional — common in localized patches. shrubs found in Illinois (Table 1). Uncommon — localized distribution or sparse. Rare — rarely found and sparse. Nomenclature used throughout this bulletin follows the Integrated Taxonomic Information System —the ITIS data- Basic highlights of this tree checklist include the listing of 29 base utilizes real-time access to the most current and accept- native hawthorns (Crataegus), 21 native oaks (Quercus), 11 ed taxonomy based on scientific consensus. -
Lauraceae – Laurel Family
LAURACEAE – LAUREL FAMILY Plant: shrubs, trees and some vines Stem: sometimes with aromatic bark Root: Leaves: mostly evergreen, some deciduous; simple with no teeth, often elliptical and somewhat leathery; mostly alternate, less often opposite or whorled; pinnately veined with curved side veins; no stipules; sometimes glandular and aromatic Flowers: perfect but occasionally imperfect (dioecious), regular (actinomorphic); mostly in small clusters along twigs, often yellowish; tepals with 4-6 members in 2 cycles; 3-12-many, but often 9 stamens; ovary superior or inferior,1 carpel, 1 pistil Fruit: berry or drupe, single large seed Other: mostly tropical; locally, sassafras and spicebush common; Dicotyledons Group Genera: 55+ genera; locally Lindera (spice-bush), Persea, Sassafras (sassafras) WARNING – family descriptions are only a layman’s guide and should not be used as definitive LAURACEAE – LAUREL FAMILY [Northern] Spicebush; Lindera benzoin (L.) Blume Sassafras; Sassafras albidum (Nutt.) Nees [Northern] Spicebush USDA Lindera benzoin (L.) Blume Lauraceae (Laurel Family) Oak Openings Metropark, Lucas County, Ohio Notes: shrub; flowers yellow (prior to leaves), in clusters (dioecious); leaves ovate, entire, shiny green above, somewhat whitened below; bark ‘warty’ (pores); winter buds green, stalked, in alternate clusters; twigs hairy or not, often greenish; fruit a red berry or drupe; aromatic; spring [V Max Brown, 2005] Sassafras USDA Sassafras albidum (Nutt.) Nees Lauraceae (Laurel Family) Oak Openings Metropark, Lucas County, Ohio Notes: shrub or tree; flowers small and yellow; leaves alternate, lobed or not (variable), aromatic; bark deeply grooved and ridged; twigs often green (hairy or not – varieties); fruit a blue to purple drupe on red pedicel; spring [V Max Brown, 2005]. -
Morphological Nature of Floral Cup in Lauraceae
l~Yoc. Indian Acad. Sci., Vol. 88 B, Part iI, Number 4, July 1979, pp. 277-281, @ printed in India. Morphological nature of floral cup in Lauraceae S PAL School of Plant Morphology, Meerut College, Meerut 250 001 MS received 19 June 1978 Abstract. On the basis of anatomical criteria the floral cup of Lauraceae can be regarded as appendicular, as the traces entering into the floral cup are morphologi- cally compound, differentiated into tepal and stamen traces at higher levels. The ontogenetic studies also support this contention. The term Perigynous hypanthium is retained for the floral cup of Lauraceae as it is formed as a result of intercalary growth occurring underneath the region of perianth and androecium. Keywords. Lauraceae; floral cup; morphological nature; appendicular; peri- gynous hypanthium. 1. Introduction The family Lauraceae has received comparatively little attention from earlier workers because of difficulty in procuring the material. So far very little work has been done on the floral anatomy of this family (Reece 1939 ; Sastri 1952 ; Pal 1974). There has been considerable difference of opinion regarding the nature of floral cup in angiosperms. The present work was initiated to study the morphological nature of the floral cup. 2. Materials and methods The present investigation embodies the results of observations on 21 species of the Lauraceae. The material of Machilus duthiei King ex Hook.f., M. odoratissima Nees, Persea gratissima Gaertn.f., Phoebe cooperiana Kanjilal and Das, P. goal- parensis Hutch., P. hainesiana Brandis, Alseodaphne keenanii Gamble, A. owdeni Parker, Cinnamomum camphora Nees and Eberm, C. cecidodaphne Meissn., C. tamala Nees and Eberm, C. -
(Myrtaceae) from Borneo
Gardens' Bulletin Singapore 57 (2005) 269-278 269 New Tristaniopsis Peter G.Wilson & J.T.Waterh. (Myrtaceae) From Borneo P. S. ASHTON Arnold Arboretum, Harvard University, 22 Divinity Avenue Cambridge MA 02138, U.S.A. and Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AB, U.K. Abstract Three new species, Tristaniopsis kinabaluensis P.S.Ashton, T. microcmpa P.S.Ashton and T. wbiginosa S.Teo ex P.S.Ashton, and three new subspecies, Tristaniopsis kinabaluensis ssp. silamensis P.S.Ashton, T. merguensis ssp. tavaiensis P.S.Ashton and T. whitiana ssp. monostemon P.S.Aston, are described from northern Borneo, in preparation for a treatment of the Myrtaceae for the Tree Flora of Sabah and Sarawak. Introduction Species definition in Tristaniopsis Peter G.Wilson & J.T.Waterh. (formerly Tristania R. Br.) has proven to be even more difficult in Borneo than among the notorious and much larger myrtaceous genus Syzygium Gaertn. Leaf size and shape is variable. The number of stamens, which are clustered opposite the petals, is characteristic of each species but, although at most 10 per cluster, may vary in exceptional cases. Here, we adopt a conservative species concept, awaiting regional monographic and phylogenetic research. Eventually, and with further flowering collections, some at least of the infrapecific taxa described here may be raised to species rank. All specimens examined have been at the Kew herbarium unless otherwise stated. 1. Tristaniopsis kinabaluensis P.S.Ashton, sp. llOV. T. m.erguensis affinis, foliis minoribus basim versus subsessilibus attenuatis vel anguste obtusis baud auriculatis, subtus hebete glaucescentibus, staminibus 3(-5) in fasciculis, fructibus ad 5 x 4 mm minoribus facile 270 Card. -
The Laurel Or Bay Forests of the Canary Islands
California Avocado Society 1989 Yearbook 73:145-147 The Laurel or Bay Forests of the Canary Islands C.A. Schroeder Department of Biology, University of California, Los Angeles The Canary Islands, located about 800 miles southwest of the Strait of Gibraltar, are operated under the government of Spain. There are five islands which extend from 15 °W to 18 °W longitude and between 29° and 28° North latitude. The climate is Mediterranean. The two eastern islands, Fuerteventura and Lanzarote, are affected by the Sahara Desert of the mainland; hence they are relatively barren and very arid. The northeast trade winds bring moisture from the sea to the western islands of Hierro, Gomera, La Palma, Tenerife, and Gran Canaria. The southern ends of these islands are in rain shadows, hence are dry, while the northern parts support a more luxuriant vegetation. The Canary Islands were prominent in the explorations of Christopher Columbus, who stopped at Gomera to outfit and supply his fleet prior to sailing "off the map" to the New World in 1492. Return voyages by Columbus and other early explorers were via the Canary Islands, hence many plants from the New World were first established at these points in the Old World. It is suspected that possibly some of the oldest potato germplasm still exists in these islands. Man exploited the islands by growing sugar cane, and later Mesembryanthemum crystallinum for the extraction of soda, cochineal cactus, tomatoes, potatoes, and finally bananas. The banana industry is slowly giving way to floral crops such as strelitzia, carnations, chrysanthemums, and several new exotic fruits such as avocado, mango, papaya, and carambola. -
Computer Vision Cracks the Leaf Code
Computer vision cracks the leaf code Peter Wilfa,1, Shengping Zhangb,c,1, Sharat Chikkerurd, Stefan A. Littlea,e, Scott L. Wingf, and Thomas Serreb,1 aDepartment of Geosciences, Pennsylvania State University, University Park, PA 16802; bDepartment of Cognitive, Linguistic and Psychological Sciences, Brown Institute for Brain Science, Brown University, Providence, RI 02912; cSchool of Computer Science and Technology, Harbin Institute of Technology, Weihai 264209, Shandong, People’s Republic of China; dAzure Machine Learning, Microsoft, Cambridge, MA 02142; eLaboratoire Ecologie, Systématique et Evolution, Université Paris-Sud, 91405 Orsay Cedex, France; and fDepartment of Paleobiology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013 Edited by Andrew H. Knoll, Harvard University, Cambridge, MA, and approved February 1, 2016 (received for review December 14, 2015) Understanding the extremely variable, complex shape and venation species (15–19), and there is community interest in approaching this characters of angiosperm leaves is one of the most challenging problem through crowd-sourcing of images and machine-identifi- problems in botany. Machine learning offers opportunities to analyze cation contests (see www.imageclef.org). Nevertheless, very few large numbers of specimens, to discover novel leaf features of studies have made use of leaf venation (20, 21), and none has angiosperm clades that may have phylogenetic significance, and to attempted automated learning and classification above the species use those characters to classify unknowns. Previous computer vision level that may reveal characters with evolutionary significance. approaches have primarily focused on leaf identification at the species There is a developing literature on extraction and quantitative level. It remains an open question whether learning and classification analyses of whole-leaf venation networks (22–25). -
Recommended Street Tree Species List San Francisco Urban Forestry Council
Recommended Street Tree Species List San Francisco Urban Forestry Council The Urban Forestry Council annually reviews and updates this list of trees, in collaboration with public and non-profit urban forestry stakeholders, including San Francisco’s Department of Public Works Urban Forestry Division and Friends of the Urban Forest. It’s important to carefully match the conditions of your site with the tree you choose. Please note that while this list contains recommendations that are known to do well in many locations in San Francisco, no tree is perfect for every potential tree planting location in San Francisco. This list should be used as a guideline for choosing which street tree to plant, but should not be used without the help of a tree professional. Species that perform well in many locations in San Francisco Evergreen Deciduous Arbutus x ‘Marina’ Prunus cerasifera ‘Krauter Vesuvius’ Callistemon citrinus Prunus serrulata ‘Kwanzan’ Callistemon viminalis Pyrus calleryana ‘Chanticleer’ Cordyline australis Small Eriobotrya deflexa Magnolia grandiflora ‘St. Mary,’ ‘Little Gem’ Pyrus kawakamii Tristaniopsis laurina Tristaniopsis laurina ‘Elegant’ Evergreen Deciduous Melaleuca linarifolia Pyrus calleryana ‘Aristocrat’ Melaleuca quinquenervia Metrosideros excelsus Medium Olea europaea Trachycarpus fortunei Evergreen Deciduous Lagunaria patersonii Ginkgo biloba ‘Autumn Gold’, ‘Saratoga’ Lophostemon confertus (formerly Tristania Platanus x acerifolia ‘Bloodgood,’ ‘Yarwood’ conferta) Tilia cordata Large Magnolia grandiflora ‘Sam Sommers,’ -
Brisbane Native Plants by Suburb
INDEX - BRISBANE SUBURBS SPECIES LIST Acacia Ridge. ...........15 Chelmer ...................14 Hamilton. .................10 Mayne. .................25 Pullenvale............... 22 Toowong ....................46 Albion .......................25 Chermside West .11 Hawthorne................. 7 McDowall. ..............6 Torwood .....................47 Alderley ....................45 Clayfield ..................14 Heathwood.... 34. Meeandah.............. 2 Queensport ............32 Trinder Park ...............32 Algester.................... 15 Coopers Plains........32 Hemmant. .................32 Merthyr .................7 Annerley ...................32 Coorparoo ................3 Hendra. .................10 Middle Park .........19 Rainworth. ..............47 Underwood. ................41 Anstead ....................17 Corinda. ..................14 Herston ....................5 Milton ...................46 Ransome. ................32 Upper Brookfield .......23 Archerfield ...............32 Highgate Hill. ........43 Mitchelton ...........45 Red Hill.................... 43 Upper Mt gravatt. .......15 Ascot. .......................36 Darra .......................33 Hill End ..................45 Moggill. .................20 Richlands ................34 Ashgrove. ................26 Deagon ....................2 Holland Park........... 3 Moorooka. ............32 River Hills................ 19 Virginia ........................31 Aspley ......................31 Doboy ......................2 Morningside. .........3 Robertson ................42 Auchenflower -
Bignoniaceae)
Systematic Botany (2007), 32(3): pp. 660–670 # Copyright 2007 by the American Society of Plant Taxonomists Taxonomic Revisions in the Polyphyletic Genus Tabebuia s. l. (Bignoniaceae) SUSAN O. GROSE1 and R. G. OLMSTEAD Department of Biology, University of Washington, Box 355325, Seattle, Washington 98195 U.S.A. 1Author for correspondence ([email protected]) Communicating Editor: James F. Smith ABSTRACT. Recent molecular studies have shown Tabebuia to be polyphyletic, thus necessitating taxonomic revision. These revisions are made here by resurrecting two genera to contain segregate clades of Tabebuia. Roseodendron Miranda consists of the two species with spathaceous calices of similar texture to the corolla. Handroanthus Mattos comprises the principally yellow flowered species with an indumentum of hairs covering the leaves and calyx. The species of Handroanthus are also characterized by having extremely dense wood containing copious quantities of lapachol. Tabebuia is restricted to those species with white to red or rarely yellow flowers and having an indumentum of stalked or sessile lepidote scales. The following new combinations are published: Handroanthus arianeae (A. H. Gentry) S. Grose, H. billbergii (Bur. & K. Schum). S. Grose subsp. billbergii, H. billbergii subsp. ampla (A. H. Gentry) S. Grose, H. botelhensis (A. H. Gentry) S. Grose, H. bureavii (Sandwith) S. Grose, H. catarinensis (A. H. Gentry) S. Grose, H. chrysanthus (Jacq.) S. Grose subsp. chrysanthus, H. chrysanthus subsp. meridionalis (A. H. Gentry) S. Grose, H. chrysanthus subsp. pluvicolus (A. H. Gentry) S. Grose, H. coralibe (Standl.) S. Grose, H. cristatus (A. H. Gentry) S. Grose, H. guayacan (Seemann) S. Grose, H. incanus (A. H. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000).