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Department of Planning and Zoning
Department of Planning and Zoning Subject: Howard County Landscape Manual Updates: Recommended Street Tree List (Appendix B) and Recommended Plant List (Appendix C) - Effective July 1, 2010 To: DLD Review Staff Homebuilders Committee From: Kent Sheubrooks, Acting Chief Division of Land Development Date: July 1, 2010 Purpose: The purpose of this policy memorandum is to update the Recommended Plant Lists presently contained in the Landscape Manual. The plant lists were created for the first edition of the Manual in 1993 before information was available about invasive qualities of certain recommended plants contained in those lists (Norway Maple, Bradford Pear, etc.). Additionally, diseases and pests have made some other plants undesirable (Ash, Austrian Pine, etc.). The Howard County General Plan 2000 and subsequent environmental and community planning publications such as the Route 1 and Route 40 Manuals and the Green Neighborhood Design Guidelines have promoted the desirability of using native plants in landscape plantings. Therefore, this policy seeks to update the Recommended Plant Lists by identifying invasive plant species and disease or pest ridden plants for their removal and prohibition from further planting in Howard County and to add other available native plants which have desirable characteristics for street tree or general landscape use for inclusion on the Recommended Plant Lists. Please note that a comprehensive review of the street tree and landscape tree lists were conducted for the purpose of this update, however, only -
Seeds of Oxyccocus Palustris Pers. from Ericaceae Family
Biology of germination of medicinal plant seeds. Part XXIII: Seeds of Oxyccocus palustris Pers. from Ericaceae family WALDEMAR BUCHWALD*, JAN KOZŁOWSKI, ELŻBIETA BILIŃSKA The Branch of Medicinal Plants of the Institute of Natural Fibres and Medicinal Plants Libelta 27 61-707 Poznań, Poland *corresponding author: [email protected], phone: +4861 6517190, fax: +4861 6517192 S u m m a r y At the beginning a short characteristic of Ericaceae family is elaborated then the biology of seeds germination of Oxyccocus palustris Pers. is described. In this experiments, the opti- mal condition of ability of germination of Oxyccocus palustris Pers. was established. It was found that the light and variable temperature (30oC over 8 hours, 20oC over 16 hours) were optimal for analysis of Oxyccocus palustris seed germination ability. The results also show that the pre-sowing treatments (stratification) were significant to obtain a higher percent of germinating seeds in comparison to non-stratified seeds. The capacity of germination of Oxyccocus palustris Pers. seeds stored in unheated room conditions gradually decreased in the first year after harvest. The viability of Oxyccocus palustris seeds is very short. Three years after harvest time, the seeds do not germinate. Key words: Ericaceae family, Oxyccocus palustris Pers., germination, seeds INTRODUCTION The characteristics of Ericaceae family In Poland 15 species from 10 genera belonging to Ericaceae family are noticed [1-5]. It is relatively few taxa in comparison to 82 genera and to over 2,500 species widespread all over the world. The plants appear as a dwarf shrub, sub-shrub, shrub or a small tree, usually with alternating leathery and often evergreen leaves. -
5 Fagaceae Trees
CHAPTER 5 5 Fagaceae Trees Antoine Kremerl, Manuela Casasoli2,Teresa ~arreneche~,Catherine Bod6n2s1, Paul Sisco4,Thomas ~ubisiak~,Marta Scalfi6, Stefano Leonardi6,Erica ~akker~,Joukje ~uiteveld', Jeanne ~omero-Seversong, Kathiravetpillai Arumuganathanlo, Jeremy ~eror~',Caroline scotti-~aintagne", Guy Roussell, Maria Evangelista Bertocchil, Christian kxerl2,Ilga porth13, Fred ~ebard'~,Catherine clark15, John carlson16, Christophe Plomionl, Hans-Peter Koelewijn8, and Fiorella villani17 UMR Biodiversiti Genes & Communautis, INRA, 69 Route d'Arcachon, 33612 Cestas, France, e-mail: [email protected] Dipartimento di Biologia Vegetale, Universita "La Sapienza", Piazza A. Moro 5,00185 Rome, Italy Unite de Recherche sur les Especes Fruitikres et la Vigne, INRA, 71 Avenue Edouard Bourlaux, 33883 Villenave d'Ornon, France The American Chestnut Foundation, One Oak Plaza, Suite 308 Asheville, NC 28801, USA Southern Institute of Forest Genetics, USDA-Forest Service, 23332 Highway 67, Saucier, MS 39574-9344, USA Dipartimento di Scienze Ambientali, Universitk di Parma, Parco Area delle Scienze 1lIA, 43100 Parma, Italy Department of Ecology and Evolution, University of Chicago, 5801 South Ellis Avenue, Chicago, IL 60637, USA Alterra Wageningen UR, Centre for Ecosystem Studies, P.O. Box 47,6700 AA Wageningen, The Netherlands Department of Biological Sciences, University of Notre Dame, Notre Dame, IN 46556, USA lo Flow Cytometry and Imaging Core Laboratory, Benaroya Research Institute at Virginia Mason, 1201 Ninth Avenue, Seattle, WA 98101, -
Native Trees of Georgia
1 NATIVE TREES OF GEORGIA By G. Norman Bishop Professor of Forestry George Foster Peabody School of Forestry University of Georgia Currently Named Daniel B. Warnell School of Forest Resources University of Georgia GEORGIA FORESTRY COMMISSION Eleventh Printing - 2001 Revised Edition 2 FOREWARD This manual has been prepared in an effort to give to those interested in the trees of Georgia a means by which they may gain a more intimate knowledge of the tree species. Of about 250 species native to the state, only 92 are described here. These were chosen for their commercial importance, distribution over the state or because of some unusual characteristic. Since the manual is intended primarily for the use of the layman, technical terms have been omitted wherever possible; however, the scientific names of the trees and the families to which they belong, have been included. It might be explained that the species are grouped by families, the name of each occurring at the top of the page over the name of the first member of that family. Also, there is included in the text, a subdivision entitled KEY CHARACTERISTICS, the purpose of which is to give the reader, all in one group, the most outstanding features whereby he may more easily recognize the tree. ACKNOWLEDGEMENTS The author wishes to express his appreciation to the Houghton Mifflin Company, publishers of Sargent’s Manual of the Trees of North America, for permission to use the cuts of all trees appearing in this manual; to B. R. Stogsdill for assistance in arranging the material; to W. -
Ohio Trees for Bees Denise Ellsworth, Department of Entomology
OHIO STATE UNIVERSITY EXTENSION AGRICULTURE AND NATURAL RESOURCES FACT SHEET ENT-71-15 Ohio Trees for Bees Denise Ellsworth, Department of Entomology Many people are concerned about the health and survival of bees, including honey bees, native bumble bees and the hundreds of lesser-known native and wild bees that call Ohio home. Bees are threatened by an assortment of factors such as pests, pathogens, pesticides, climate change and a lack of nesting habitat and forage plants. Bees and flowering plants have a critical relationship. Flowering plants provide nectar and pollen for a bee’s diet. Pollen is an essential source of protein for developing bee larvae, and nectar provides a carbohydrate source. Honey bees convert nectar into honey by adding an enzyme which breaks down the complex sugars into simple sugars. Bees, in turn, transport pollen from flower to flower as they forage, allowing for plant fertilization and the production of seeds and fruit. While trees provide many well-known ecological benefits, the importance of trees as a source of food for bees is sometimes overlooked. Ohio trees can provide food for bees from early spring through late summer, with most tree species in Ohio blooming in spring and early summer. This fact sheet describes some of the Ohio trees that provide food for bees. Trees included in this list have been described as important by multiple researchers and bee experts. Other trees not listed here can also provide food for bees. For example, Ohio horticultural experts have noted significant bee foraging activity on trees such as Carolina silverbell (Halesia carolina), seven-son flower (Heptacodium miconioides), goldenrain tree (Koelreuteria paniculata) and Japanese pagoda tree (Styphnolobium japonicum) in landscape settings. -
Amelanchierspp. Family: Rosaceae Serviceberry
Amelanchier spp. Family: Rosaceae Serviceberry The genus Amelanchier contains about 16 species native to North America [5], Mexico [2], and Eurasia to northern Africa [4]. The word amelanchier is derived from the French common name amelanche of the European serviceberry, Amelanchier ovalis. Amelanchier alnifolia-juneberry, Pacific serviceberry, pigeonberry, rocky mountain servicetree, sarvice, sarviceberry, saskatoon, saskatoon serviceberry, western service, western serviceberry , western shadbush Amelanchier arborea-Allegheny serviceberry, apple shadbush, downy serviceberry , northern smooth shadbush, shadblow, shadblown serviceberry, shadbush, shadbush serviceberry Amelanchier bartramiana-Bartram serviceberry Amelanchier canadensis-American lancewood, currant-tree, downy serviceberry, Indian cherry, Indian pear, Indian wild pear, juice plum, juneberry, may cherry, sugar plum, sarvice, servicetree, shadberry, shadblow, shadbush, shadbush serviceberry, shadflower, thicket serviceberry Amelanchier florida-Pacific serviceberry Amelanchier interior-inland serviceberry Amelanchier sanguinea-Huron serviceberry, roundleaf juneberry, roundleaf serviceberry , shore shadbush Amelanchier utahensis-Utah serviceberry Distribution In North America throughout upper elevations and temperate forests. The Tree Serviceberry is a shrub or tree that reaches a height of 40 ft (12 m) and a diameter of 2 ft (0.6 m). It grows in many soil types and occurs from swamps to mountainous hillsides. It flowers in early spring, producing delicate white flowers, making -
Oaks (Quercus Spp.): a Brief History
Publication WSFNR-20-25A April 2020 Oaks (Quercus spp.): A Brief History Dr. Kim D. Coder, Professor of Tree Biology & Health Care / University Hill Fellow University of Georgia Warnell School of Forestry & Natural Resources Quercus (oak) is the largest tree genus in temperate and sub-tropical areas of the Northern Hemisphere with an extensive distribution. (Denk et.al. 2010) Oaks are the most dominant trees of North America both in species number and biomass. (Hipp et.al. 2018) The three North America oak groups (white, red / black, and golden-cup) represent roughly 60% (~255) of the ~435 species within the Quercus genus worldwide. (Hipp et.al. 2018; McVay et.al. 2017a) Oak group development over time helped determine current species, and can suggest relationships which foster hybridization. The red / black and white oaks developed during a warm phase in global climate at high latitudes in what today is the boreal forest zone. From this northern location, both oak groups spread together southward across the continent splitting into a large eastern United States pathway, and much smaller western and far western paths. Both species groups spread into the eastern United States, then southward, and continued into Mexico and Central America as far as Columbia. (Hipp et.al. 2018) Today, Mexico is considered the world center of oak diversity. (Hipp et.al. 2018) Figure 1 shows genus, sub-genus and sections of Quercus (oak). History of Oak Species Groups Oaks developed under much different climates and environments than today. By examining how oaks developed and diversified into small, closely related groups, the native set of Georgia oak species can be better appreciated and understood in how they are related, share gene sets, or hybridize. -
Ericaceae Five Petals, Sometimes Free, Though Usually the Heather Family Fused Together to Form a Tube, Bell Or Urn
RHS GENEALOGY FOR GARDENERS EUDICOTS sepals, free or fused at the base, and four or Ericaceae five petals, sometimes free, though usually The heather family fused together to form a tube, bell or urn. The stamens are in whorls of four or five and Hugely useful in the garden, this family of mainly woody plants includes the heathers the pollen is released from the anthers by (Calluna, Erica, Daboecia), azaleas, rhododendrons, wintergreens (Gaultheria), way of pores at the tips. Pieris and mountain laurels (Kalmia). Commercially significant crops include Fruit blueberries and cranberries (Vaccinium). Fruits are typically dry capsules, though fleshy Size Origins fruits, such as blueberries, are not uncommon. One of the larger families, the Ericaceae contains Earliest evidence of this family dates to the Late Leaves over 3,850 species. Within this great diversity are Cretaceous (about 90 million years ago). Fossils many small genera with one or two species, and suggest that Ericaceae was once more diverse in Most Ericaceae have evergreen, alternate leaves and Vaccinium corymbosum, three titans; Rhododendron (with 1,000 species), Europe, which was home to genera now restricted no stipules. Some species, such as many azaleas, highbush blueberry Erica (850 species) and Vaccinium (500 species). to Asia and/or America. are deciduous, while opposite and whorled leaf It should be noted that azaleas are included arrangements are also known. Leaf margins are within Rhododendron. Flowers entire, toothed or curled under, and some species USES FOR THIS FAMILY (including many rhododendrons) have dense hair Great floral diversity is encompassed by this or scales on the lower surfaces. -
The Quarterly Journal of the Florida Native Plant Society
Volume 28: Number 1 > Winter/Spring 2011 PalmettoThe Quarterly Journal of the Florida Native Plant Society Protecting Endangered Plants in Panhandle Parks ● Native or Not? Carica papaya ● Water Science & Plants Protecting Endangered Plant Species Sweetwater slope: Bill and Pam Anderson To date, a total of 117 listed taxa have been recorded in 26 panhandle parks, making these parks a key resource for the protection of endangered plant species. 4 ● The Palmetto Volume 28:1 ● Winter/Spring 2011 in Panhandle State Parks by Gil Nelson and Tova Spector The Florida Panhandle is well known for its natural endowments, chief among which are its botanical and ecological diversity. Approximately 242 sensitive plant taxa occur in the 21 counties west of the Suwannee River. These include 15 taxa listed as endangered or threatened by the U. S. Fish and Wildlife Service (USFWS), 212 listed as endangered or threatened by the State of Florida, 191 tracked by the Florida Natural Areas Inventory, 52 candidates for federal listing, and 7 categorized by the state as commercially exploited. Since the conservation of threatened and endangered plant species depends largely on effective management of protected populations, the occurrence of such plants on publicly or privately owned conservation lands, coupled with institutional knowledge of their location and extent is essential. District 1 of the Florida Sarracenia rosea (purple pitcherplant) at Ponce de Leon Springs State Park: Park Service manages 33 state parks encompassing approximately Tova Spector, Florida Department of Environmental Protection 53,877 acres in the 18 counties from Jefferson County and the southwestern portion of Taylor County westward. -
Tracing History
Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 911 Tracing History Phylogenetic, Taxonomic, and Biogeographic Research in the Colchicum Family BY ANNIKA VINNERSTEN ACTA UNIVERSITATIS UPSALIENSIS UPPSALA 2003 Dissertation presented at Uppsala University to be publicly examined in Lindahlsalen, EBC, Uppsala, Friday, December 12, 2003 at 10:00 for the degree of Doctor of Philosophy. The examination will be conducted in English. Abstract Vinnersten, A. 2003. Tracing History. Phylogenetic, Taxonomic and Biogeographic Research in the Colchicum Family. Acta Universitatis Upsaliensis. Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 911. 33 pp. Uppsala. ISBN 91-554-5814-9 This thesis concerns the history and the intrafamilial delimitations of the plant family Colchicaceae. A phylogeny of 73 taxa representing all genera of Colchicaceae, except the monotypic Kuntheria, is presented. The molecular analysis based on three plastid regions—the rps16 intron, the atpB- rbcL intergenic spacer, and the trnL-F region—reveal the intrafamilial classification to be in need of revision. The two tribes Iphigenieae and Uvularieae are demonstrated to be paraphyletic. The well-known genus Colchicum is shown to be nested within Androcymbium, Onixotis constitutes a grade between Neodregea and Wurmbea, and Gloriosa is intermixed with species of Littonia. Two new tribes are described, Burchardieae and Tripladenieae, and the two tribes Colchiceae and Uvularieae are emended, leaving four tribes in the family. At generic level new combinations are made in Wurmbea and Gloriosa in order to render them monophyletic. The genus Androcymbium is paraphyletic in relation to Colchicum and the latter genus is therefore expanded. -
Native Nebraska Woody Plants
THE NEBRASKA STATEWIDE ARBORETUM PRESENTS NATIVE NEBRASKA WOODY PLANTS Trees (Genus/Species – Common Name) 62. Atriplex canescens - four-wing saltbrush 1. Acer glabrum - Rocky Mountain maple 63. Atriplex nuttallii - moundscale 2. Acer negundo - boxelder maple 64. Ceanothus americanus - New Jersey tea 3. Acer saccharinum - silver maple 65. Ceanothus herbaceous - inland ceanothus 4. Aesculus glabra - Ohio buckeye 66. Cephalanthus occidentalis - buttonbush 5. Asimina triloba - pawpaw 67. Cercocarpus montanus - mountain mahogany 6. Betula occidentalis - water birch 68. Chrysothamnus nauseosus - rabbitbrush 7. Betula papyrifera - paper birch 69. Chrysothamnus parryi - parry rabbitbrush 8. Carya cordiformis - bitternut hickory 70. Cornus amomum - silky (pale) dogwood 9. Carya ovata - shagbark hickory 71. Cornus drummondii - roughleaf dogwood 10. Celtis occidentalis - hackberry 72. Cornus racemosa - gray dogwood 11. Cercis canadensis - eastern redbud 73. Cornus sericea - red-stem (redosier) dogwood 12. Crataegus mollis - downy hawthorn 74. Corylus americana - American hazelnut 13. Crataegus succulenta - succulent hawthorn 75. Euonymus atropurpureus - eastern wahoo 14. Fraxinus americana - white ash 76. Juniperus communis - common juniper 15. Fraxinus pennsylvanica - green ash 77. Juniperus horizontalis - creeping juniper 16. Gleditsia triacanthos - honeylocust 78. Mahonia repens - creeping mahonia 17. Gymnocladus dioicus - Kentucky coffeetree 79. Physocarpus opulifolius - ninebark 18. Juglans nigra - black walnut 80. Prunus besseyi - western sandcherry 19. Juniperus scopulorum - Rocky Mountain juniper 81. Rhamnus lanceolata - lanceleaf buckthorn 20. Juniperus virginiana - eastern redcedar 82. Rhus aromatica - fragrant sumac 21. Malus ioensis - wild crabapple 83. Rhus copallina - flameleaf (shining) sumac 22. Morus rubra - red mulberry 84. Rhus glabra - smooth sumac 23. Ostrya virginiana - hophornbeam (ironwood) 85. Rhus trilobata - skunkbush sumac 24. Pinus flexilis - limber pine 86. Ribes americanum - wild black currant 25. -
Nutrient Foraging in Woodland Herbs: a Comparison of Three Species of Uvularia (Liliaceae) with Contrasting Belowground Morphologies1
American Journal of Botany 88(6): 1071±1079. 2001. NUTRIENT FORAGING IN WOODLAND HERBS: A COMPARISON OF THREE SPECIES OF UVULARIA (LILIACEAE) WITH CONTRASTING BELOWGROUND MORPHOLOGIES1 DUSHYANTHA K. WIJESINGHE2 AND DENNIS F. W HIGHAM3 Smithsonian Environmental Research Center, P.O. Box 28, Edgewater, Maryland 21037 USA We compared the ability of three closely related species, Uvularia perfoliata, U. sessilifolia, and U. puberula, to forage and explore patches in nutritionally homogeneous and heterogeneous environments. The species differed in type and function of plagiotropic stems and the extent of clonality and physiological integration. Our aim was to determine (1) whether selective placement of roots in high- nutrient patches, i.e., foraging, was accompanied by facilitatory morphological changes such as internode elongation or increased branching, (2) whether foraging ability of species depended on the extent of physiological integration, and (3) how variability in environmental quality in¯uenced the performance of each species. We studied the growth of each species over two seasons in exper- imental environments. Uvularia perfoliata and U. puberula foraged in high-nutrient patches in heterogeneous environments. Uvularia sessilifolia did not show selective placement of roots. The two clonal species, U. perfoliata and U. sessilifolia, did not show any changes in architectural traits predicted to facilitate foraging. The nonclonal species, U. puberula, was the strongest forager and the most physiologically integrated species, U. sessilifolia, was the weakest forager, in line with the view that physiological integration limits foraging ef®ciency. Variability in environmental quality had little effect on the performance of the three species. Yield and estimators of ®tness were not greater in treatments where more high-quality patches were encountered consecutively than in treatments where fewer high-quality patches were encountered consecutively during growth.