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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 Unpublished Report.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. -
Koelreuteria Bipinnata Chinese Flame-Tree1 Edward F
Fact Sheet ST-336 November 1993 Koelreuteria bipinnata Chinese Flame-Tree1 Edward F. Gilman and Dennis G. Watson2 INTRODUCTION A yellow carpet of fallen petals, delicate leaflets which cast a mosaic of welcoming shade, and large clusters of persistent rose-colored, papery capsules all help to make Chinese Flame-Treetree a very popular landscape tree over a wide area of the south (Fig. 1). One of only a few yellow-flowering trees for the mid- and deep-south landscape. This broad-spreading, deciduous tree reaches a height of 40 to 60 feet and eventually takes on a flat-topped, somewhat irregular silhouette. It is often used as a patio, shade, street, or specimen tree. The small, fragrant, yellow flowers appear in very showy, dense, terminal panicles in early summer, and are followed in late summer or fall by large clusters of the two-inch-long "Chinese lanterns". These papery husks are held above the foliage and retain their pink color after drying and are very popular for use in everlasting flower arrangements. The bark on Chinese Flame-Tree is smooth and light brown when young, becoming ridged and furrowed as the tree matures. Easily distinquished from Koelreuteria paniculata since Koelreuteria bipinnata has more upright branches and has twice compound leaves, whereas Koelreuteria paniculata has single pinnate compound leaves. Figure 1. Young Chinese Flame-Tree. GENERAL INFORMATION USDA hardiness zones: 7 through 10A (Fig. 2) Origin: not native to North America Scientific name: Koelreuteria bipinnata Uses: container or above-ground planter; large Pronunciation: kole-roo-TEER-ee-uh parking lot islands (> 200 square feet in size); wide bye-pih-NAY-tuh tree lawns (>6 feet wide); medium-sized parking lot Common name(s): Chinese Flame-Tree, islands (100-200 square feet in size); medium-sized Bougainvillea Goldenraintree tree lawns (4-6 feet wide); recommended for buffer Family: Sapindaceae 1. -
Koelreuteria Paniculata 'Fastigiata'
Fact Sheet ST-339 November 1993 Koelreuteria paniculata ‘Fastigiata’ ‘Fastigiata’ Goldenraintree1 Edward F. Gilman and Dennis G. Watson2 INTRODUCTION This cultivar of Goldenraintree probably grows 30 feet tall with a four to six-foot spread (Fig. 1). Although the species has a reputation for being weak wooded, this selection may stay together due to the tight, compact growth habit. It is rarely attacked by pests and grows in a wide range of soils, including high pH soils. Goldenraintree tolerates dryness and casts little shade because of the narrow growth habit. It would make a good tree particularly where overhead or soil space is limited, due to its narrow crown and adaptive abilities. The tree grows moderately and bears few flowers. It is not as showy as Koelreuteria bipinnata but is much more cold-tolerant. However, it is less cold tolerant than the species. GENERAL INFORMATION Scientific name: Koelreuteria paniculata ‘Fastigiata’ Pronunciation: kole-roo-TEER-ee-uh pan-ick-yoo-LAY-tuh Common name(s): ‘Fastigiata’ Goldenraintree Family: Sapindaceae USDA hardiness zones: 5B through 9 (Fig. 2) Origin: not native to North America Uses: wide tree lawns (>6 feet wide); medium-sized tree lawns (4-6 feet wide); recommended for buffer strips around parking lots or for median strip plantings Figure 1. Middle-aged ‘Fastigiata’ Goldenraintree. in the highway; specimen; sidewalk cutout (tree pit); residential street tree; tree has been successfully grown in urban areas where air pollution, poor drainage, compacted soil, and/or drought are common Availability: grown in small quantities by a small number of nurseries 1. This document is adapted from Fact Sheet ST-339, a series of the Environmental Horticulture Department, Florida Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida. -
Plant Pathology Circular No. 303 Fla. Dept. Agric. & Consumer Serv
Plant Pathology Circular No. 303 Fla. Dept. Agric. & Consumer Serv. January 1987 Division of Plant Industry PHYTOPHTHORA ROOT & CROWN ROT OF RADERMACHERA SINICA Robert M. Leahyl Radermachera sinica (Hance) Hemsl., a member of the Bignoniaceae, occurs naturally in India, China, Java, the Celebes and the Phillipine Islands. This plant is a relatively new introduction to the foliage market in Florida and is used most commonly as indoor accent plants. Radermachera sinica is easy to grow and can be propagated by cuttings, marcottage and seed (1). SYMPTOMS: Few diseases are recorded on Radermachera sinica; however, Phytophthora parasitica Dastur, which has a wide host range, can cause a serious root and stem rot. It is also quite aggressive as a damping off disease of Radermachera seedlings. (DPI, Plant Pathology Files, UNPBL.). Phytophthora parasitica infects the young tender roots and stem tissue of seedlings resulting in their collapse and death. Overfertilization and poorly drained/overwatered media can play an important role in predisposing these plants to infection by Phytophthora. Older, more established Radermachera plants can also fall prey to this disease; however, symptoms tend to be less obvious at the initial onset of infection. Infected R. sinica plants eventually become unthrifty and chlorotic. Defoliation occurs as symptoms progress and eventually stems become necrotic. This gives infected plants an overall thin, flagged appearance. Fig. 1. Defoliation, col- lapsed foliage and blight- ed stems are symptoms ex- pressed by the infected Radermachera seedling on the left. (DPI Photo #87131 by Jeffrey W. Lotz). 1Biological Scientist II, Bureau of Plant Pathology, P. O. Box 1269, Gainesville, F1 32602. -
Environmental Weeds of Coastal Plains and Heathy Forests Bioregions of Victoria Heading in Band
Advisory list of environmental weeds of coastal plains and heathy forests bioregions of Victoria Heading in band b Advisory list of environmental weeds of coastal plains and heathy forests bioregions of Victoria Heading in band Advisory list of environmental weeds of coastal plains and heathy forests bioregions of Victoria Contents Introduction 1 Purpose of the list 1 Limitations 1 Relationship to statutory lists 1 Composition of the list and assessment of taxa 2 Categories of environmental weeds 5 Arrangement of the list 5 Column 1: Botanical Name 5 Column 2: Common Name 5 Column 3: Ranking Score 5 Column 4: Listed in the CALP Act 1994 5 Column 5: Victorian Alert Weed 5 Column 6: National Alert Weed 5 Column 7: Weed of National Significance 5 Statistics 5 Further information & feedback 6 Your involvement 6 Links 6 Weed identification texts 6 Citation 6 Acknowledgments 6 Bibliography 6 Census reference 6 Appendix 1 Environmental weeds of coastal plains and heathy forests bioregions of Victoria listed alphabetically within risk categories. 7 Appendix 2 Environmental weeds of coastal plains and heathy forests bioregions of Victoria listed by botanical name. 19 Appendix 3 Environmental weeds of coastal plains and heathy forests bioregions of Victoria listed by common name. 31 Advisory list of environmental weeds of coastal plains and heathy forests bioregions of Victoria i Published by the Victorian Government Department of Sustainability and Environment Melbourne, March2008 © The State of Victoria Department of Sustainability and Environment 2009 This publication is copyright. No part may be reproduced by any process except in accordance with the provisions of the Copyright Act 1968. -
Coleeae: Crescentieae: Oroxyleae
Gasson & Dobbins - Trees versus lianas in Bignoniaceae 415 Schenck, H. 1893. Beitriige zur Anatomie Takhtajan, A. 1987. Systema Magnoliophy der Lianen. In: A.F.W. Schimper (ed.): torum. Academia Scientiarum U.R.S.S., 1-271. Bot. Mitt. aus den Tropen. Heft Leningrad. 5, Teil2. Gustav Fischer, Jena. Wheeler, E.A., R.G. Pearson, C.A. La Spackman, W. & B.G.L. Swamy. 1949. The Pasha, T. Zack & W. Hatley. 1986. Com nature and occurrence of septate fibres in puter-aided Wood Identification. Refer dicotyledons. Amer. 1. Bot. 36: 804 (ab ence Manual. North Carolina Agricultural stract). Research Service Bulletin 474. Sprague, T. 1906. Flora of Tropical Africa. Willis, J. C. 1973. A dictionary of the flower Vol. IV, Sect. 2, Hydrophyllaceae to. Pe ing plants. Revised by H. K. Airy Shaw. daliaceae. XCVI, Bignoniaceae: 512-538. 8th Ed. Cambridge Univ. Press. Steenis, C.G.G.J. van. 1977. Bignoniaceae. Wolkinger, F. 1970. Das Vorkommen leben In Flora Malesiana I, 8 (2): 114-186. der Holzfasem in Striiuchem und Bliumen. Sijthoff & Noordhoff, The Netherlands. Phyton (Austria) 14: 55-67. Stem, W. L. 1988. Index Xylariorum 3. In Zimmermann, M.H. 1983. Xylem structure stitutional wood collections of the world. and the ascent of sap. Springer Verlag, IAWA Bull. n.s. 9: 203-252. Berlin, Heidelberg, New York, Tokyo. APPENDIX The species examined are listed below. The country or geographical region of origin is that from which the specimen came, not necessarily its native habitat. If the exact source of the specimen is not known, but the native region is, this is in parentheses. -
(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. -
Delimitation of Malagasy Tribe Coleeae and Implications for Fruit Evolution in Bignoniaceae Inferred from a Chloroplast DNA Phylogeny
Plant Syst. Evol. 245: 55–67 (2004) DOI 10.1007/s00606-003-0025-y Delimitation of Malagasy tribe Coleeae and implications for fruit evolution in Bignoniaceae inferred from a chloroplast DNA phylogeny M. L. Zjhra1, K. J. Sytsma2, and R. G. Olmstead3 1Department of Biology, Georgia Southern University, Statesboro, GA, USA 2Department of Botany, University of Wisconsin, Madison, WI, USA 3Department of Botany, University of Washington, Seattle, WA, USA Received February 2, 2003; accepted April 23, 2003 Published online: February 23, 2004 Ó Springer-Verlag 2004 Abstract. Coleeae (Bignoniaceae) are a tribe almost the Gondwanan continent, Madagascar was entirely restricted to Madagascar. Coleeae have attached to Africa at present day Somalia, previously been placed in neotropical Crescentieae Kenya and Tanzania until 165 mya (Rabino- due to species with indehiscent fruits, a character witz et al. 1982, 1983). Madagascar was otherwise unusual in Bignoniaceae. A phylogeny completely separated from Africa by ndh trn based on three chloroplast regions ( F, T-L 120 mya (Rabinowitz et al. 1983), but spacer, trnL-F spacer) identifies a monophyletic remained attached to India until 88 mya Coleeae that is endemic to Madagascar and sur- rounding islands of the Indian Ocean (Seychelles, (Storey et al. 1995). During the lower Creta- Comores and Mascarenes). African Kigelia is not a ceous Madagascar traveled to its present member of Coleeae, rather it is more closely related position 400 km off the coast of Mozambique to a subset of African and Southeast Asian species (Fig. 1). The granitic islands of the Seychelles, of Tecomeae. The molecular phylogeny indicates in the Indian Ocean north of Madagascar, that indehiscent fruit have arisen repeatedly in represent fragments of the separation of Mad- Bignoniaceae: in Coleeae, Kigelia and Crescentieae. -
The Brahea Edulis Palm Forest in Guadalupe Island: a North American Fog Oasis? Revista Chilena De Historia Natural, Vol
Revista Chilena de Historia Natural ISSN: 0716-078X [email protected] Sociedad de Biología de Chile Chile GARCILLÁN, PEDRO P.; VEGA, ERNESTO; MARTORELL, CARLOS The Brahea edulis palm forest in Guadalupe Island: A North American fog oasis? Revista Chilena de Historia Natural, vol. 85, núm. 1, 2012, pp. 137-145 Sociedad de Biología de Chile Santiago, Chile Available in: http://www.redalyc.org/articulo.oa?id=369944300011 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative THE BRAHEA EDULIS PALM FOREST: A FOG OASIS? 137 REVISTA CHILENA DE HISTORIA NATURAL Revista Chilena de Historia Natural 85: 137-145, 2012 © Sociedad de Biología de Chile RESEARCH ARTICLE The Brahea edulis palm forest in Guadalupe Island: A North American fog oasis? El palmar de Brahea edulis de Isla Guadalupe: ¿Un oasis de niebla en Norteamérica? PEDRO P. GARCILLÁN1, ERNESTO VEGA2 & CARLOS MARTORELL3, * 1Centro de Investigaciones Biológicas del Noroeste (CIBNOR), Mar Bermejo No. 195, Col. Playa Palo de Santa Rita, Apdo. Postal 128, La Paz, Baja California Sur 23090, México 2Centro de Investigaciones en Ecosistemas (CIEco), Universidad Nacional Autónoma de México, Antigua Carretera a Pátzcuaro No. 8701, Col. Ex-Hacienda de San José de La Huerta C.P. 58190 Morelia, Michoacán, México 3Departamento de Ecología y Recursos Naturales, Facultad de Ciencias, Universidad Nacional Autónoma de México, Circuito Exterior s/n, Ciudad Universitaria, 04510 México D.F., México *Corresponding author: [email protected] ABSTRACT Fog is a factor that affects deeply the structure of vegetation of coastal deserts. -
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,’ -
Rdna) Organisation
OPEN Heredity (2013) 111, 23–33 & 2013 Macmillan Publishers Limited All rights reserved 0018-067X/13 www.nature.com/hdy ORIGINAL ARTICLE Dancing together and separate again: gymnosperms exhibit frequent changes of fundamental 5S and 35S rRNA gene (rDNA) organisation S Garcia1 and A Kovarˇı´k2 In higher eukaryotes, the 5S rRNA genes occur in tandem units and are arranged either separately (S-type arrangement) or linked to other repeated genes, in most cases to rDNA locus encoding 18S–5.8S–26S genes (L-type arrangement). Here we used Southern blot hybridisation, PCR and sequencing approaches to analyse genomic organisation of rRNA genes in all large gymnosperm groups, including Coniferales, Ginkgoales, Gnetales and Cycadales. The data are provided for 27 species (21 genera). The 5S units linked to the 35S rDNA units occur in some but not all Gnetales, Coniferales and in Ginkgo (B30% of the species analysed), while the remaining exhibit separate organisation. The linked 5S rRNA genes may occur as single-copy insertions or as short tandems embedded in the 26S–18S rDNA intergenic spacer (IGS). The 5S transcript may be encoded by the same (Ginkgo, Ephedra) or opposite (Podocarpus) DNA strand as the 18S–5.8S–26S genes. In addition, pseudogenised 5S copies were also found in some IGS types. Both L- and S-type units have been largely homogenised across the genomes. Phylogenetic relationships based on the comparison of 5S coding sequences suggest that the 5S genes independently inserted IGS at least three times in the course of gymnosperm evolution. Frequent transpositions and rearrangements of basic units indicate relatively relaxed selection pressures imposed on genomic organisation of 5S genes in plants. -
Columnar Plants Can with Grey-Green Foliage
Small urban lots place many constraints *Juniperus communis ‘Compressa’- Conical, on plant selection. Columnar plants can with grey-green foliage. Slow growing (3-6”/ be strategic solutions for these situations. year) reaching 2’ tall and 6” wide in ten years. In addition, tall and narrow shapes *Juniperus communis ‘Gold Cone’- Bright yellow foliage in spring and summer. Grows 3- provide a very strong structural element 6”/year reaching 6’ tall and 2’ wide. Needs full to gardens of all sizes. The following list sun and good drainage. offers some suggestions of columnar to *Picea glauca ‘Conica’- Dwarf Alberta Spruce. conical (cone-shaped) plants for a tight Cone-shaped plant with compact foliage. area. Grows 3”/year, to 8’-12’ tall and 3-5’ wide. Requires full sun. Plants are subject to seasonal availability. *Pinus sylvestris ‘Sentinel’- A dwarf, narrow Plants with an * are evergreen. form of Scott's pine with bluish needles and PLANTS 10-20’ TALL reddish bark. Slow growing to 4’ tall and 1’ wide in ten years. Needs full sun and good *Chamaecyparis obtusa ‘Gracilis’- Slender PLANTS 10’ TALL & UNDER drainage. Hinoki Cypress. Artistic structure complimented *Taxus baccata ‘Amersfoort’- An unusual by dark green, fan-like foliage. Grows 3-6”/year *Buxus semp. ‘Graham Blandy’- A narrow yew with stubby, wide needles and distinctive reaching 20’ tall and 4-5’ wide. It can reach 30’ form of English boxwood. Grows 3-6”/year in structure. Grows 1-3”/year (no information on in time. Full sun to part shade. Good drainage. height. But is no wider than 3’.