Hamamelidaceae, Part 1: Exploring the Witch-Hazels of the Arnold Arboretum
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Phytophthora Ramorum Sudden Oak Death Pathogen
NAME OF SPECIES: Phytophthora ramorum Sudden Oak Death pathogen Synonyms: Common Name: Sudden Oak Death pathogen A. CURRENT STATUS AND DISTRIBUTION I. In Wisconsin? 1. YES NO X 2. Abundance: 3. Geographic Range: 4. Habitat Invaded: 5. Historical Status and Rate of Spread in Wisconsin: 6. Proportion of potential range occupied: II. Invasive in Similar Climate YES NO X Zones United States: In 14 coastal California Counties and in Curry County, Oregon. In nursery in Washington. Canada: Nursery in British Columbia. Europe: Germany, the Netherlands, the United Kingdom, Poland, Spain, France, Belgium, and Sweden. III. Invasive in Similar Habitat YES X NO Types IV. Habitat Affected 1. Habitat affected: this disease thrives in cool, wet climates including areas in coastal California within the fog belt or in low- lying forested areas along stream beds and other bodies of water. Oaks associated with understory species that are susceptible to foliar infections are at higher risk of becoming infected. 2. Host plants: Forty-five hosts are regulated for this disease. These hosts have been found naturally infected by P. ramorum and have had Koch’s postulates completed, reviewed and accepted. Approximately fifty-nine species are associated with Phytophthora ramorum. These species are found naturally infected; P. ramorum has been cultured or detected with PCR but Koch’s postulates have not been completed or documented and reviewed. Northern red oak (Quercus rubra) is considered an associated host. See end of document for complete list of plant hosts. National Risk Model and Map shows susceptible forest types in the mid-Atlantic region of the United States. -
Colored Illustrations and Popular Descriptions of Plants
ADDISONIA COLORED ILLUSTRATIONS AND POPULAR DESCRIPTIONS OP PLANTS Volume 3 1918 BOTA' 3CAL PUBLISHED BY THE NEW YORK BOTANICAL GARDEN (ADDISON BROWN FUND) PRESS OF THE NEW ERA PRINTINQ COMPANY LANCASTER, PA. m CONTENTS Part 1 March 30, 1918 platb pagb 81 Aronia atropurpurea 1 82 Aster Novae-Angliae 3 83A Gymnocalycium multiflorum 5 83B Gymnocalycium Mostii 5 84 Euonymus alata 7 85 Diospyros virginiana 9 86 Lepadena marginata 11 87 Maackia amurensis Buergeri 13 88 Hibiscus oculiroseus 15 89 Comus ofl&cinalis 17 90 Opuntia lasiacantha 19 Part 2 June 29, 1918 91 Cotoneaster Simonsii 21 92 Echeveria nodulosa 23 93 Helianthus orgyalis 25 94 Symphoricarpos albus laevigatus 27 95 Sinningia speciosa 29 96 Stylophorum diphyllum 31 97 Aronia arbutifolia 33 98 Hamamelis japonica 35 99 Hibiscus Moscheutos 37 100 Sobralia sessilis 39 Part 3 September 30, 1918 101 Comus Mas 41 102 Solidago squarrosa 43 103 Callicarpa japonica 45 104 Aster laevis 47 105 Opuntia Opuntia .49 106 Ilex serrata argutidens 51 107 Othonna crassifolia 53 108 Magnolia Kobus 55 109 Crassula portulacea 57 110 Viburnum prunifolium 59 «•• lU iv Addisonia Part 4 December 31, 1918 111 Symphoricarpos Symphoricarpos 61 112 Spiraea Thunbergii 63 j 113 Coreopsis Leavenworthii 65 114 Echinacea purpurea 67 115 Lantana 69 depressa ; 116 Ilex verticillata 71 j 117 Vioma Baldwinii 73 ] 118 Jussiaea peruviana 75 i 119 Salvia farinacea 77 i 120 Dianthera crassifolia 79 i Index 81 i 1 ADDISONIA COLORED ILLUSTRATIONS AND POPULAR DESCRIPTIONS OF PLANTS Volume 3 Number i MARCH, 1918 PUBLISHED BY -
Scientific Name Common Name NATURAL ASSOCIATIONS of TREES and SHRUBS for the PIEDMONT a List
www.rainscapes.org NATURAL ASSOCIATIONS OF TREES AND SHRUBS FOR THE PIEDMONT A list of plants which are naturally found growing with each other and which adapted to the similar growing conditions to each other Scientific Name Common Name Acer buergeranum Trident maple Acer saccarum Sugar maple Acer rubrum Red Maple Betula nigra River birch Trees Cornus florida Flowering dogwood Fagus grandifolia American beech Maple Woods Liriodendron tulipifera Tulip-tree, yellow poplar Liquidamber styraciflua Sweetgum Magnolia grandiflora Southern magnolia Amelanchier arborea Juneberry, Shadbush, Servicetree Hamamelis virginiana Autumn Witchhazel Shrubs Ilex opaca American holly Ilex vomitoria*** Yaupon Holly Viburnum acerifolium Maple leaf viburnum Aesulus parvilflora Bottlebrush buckeye Aesulus pavia Red buckeye Carya ovata Shadbark hickory Cornus florida Flowering dogwood Halesia carolina Crolina silverbell Ilex cassine Cassina, Dahoon Ilex opaca American Holly Liriodendron tulipifera Tulip-tree, yellow poplar Trees Ostrya virginiana Ironwood Prunus serotina Wild black cherry Quercus alba While oak Quercus coccinea Scarlet oak Oak Woods Quercus falcata Spanish red oak Quercus palustris Pin oak Quercus rubra Red oak Quercus velutina Black oak Sassafras albidum Sassafras Azalea nudiflorum Pinxterbloom azalea Azalea canescens Piedmont azalea Ilex verticillata Winterberry Kalmia latifolia Mountain laurel Shrubs Rhododenron calendulaceum Flame azalea Rhus copallina Staghorn sumac Rhus typhina Shining sumac Vaccinium pensylvanicum Low-bush blueberry Magnolia -
Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese -
Tree of the Year: Liquidambar Eric Hsu and Susyn Andrews
Tree of the Year: Liquidambar Eric Hsu and Susyn Andrews With contributions from Anne Boscawen (UK), John Bulmer (UK), Koen Camelbeke (Belgium), John Gammon (UK), Hugh Glen (South Africa), Philippe de Spoelberch (Belgium), Dick van Hoey Smith (The Netherlands), Robert Vernon (UK) and Ulrich Würth (Germany). Affinities, generic distribution and fossil record Liquidambar L. has close taxonomic affinities with Altingia Noronha since these two genera share gum ducts associated with vascular bundles, terminal buds enclosed within numerous bud scales, spirally arranged stipulate leaves, poly- porate (with several pore-like apertures) pollen grains, condensed bisexual inflorescences, perfect or imperfect flowers, and winged seeds. Not surpris- ingly, Liquidambar, Altingia and Semiliquidambar H.T. Chang have now been placed in the Altingiaceae, as originally treated (Blume 1828, Wilson 1905, Chang 1964, Melikan 1973, Li et al. 1988, Zhou & Jiang 1990, Wang 1992, Qui et al. 1998, APG 1998, Judd et al. 1999, Shi et al. 2001 and V. Savolainen pers. comm.). These three genera were placed in the subfamily Altingioideae in Hamamelidaceae (Reinsch 1890, Chang 1979, Cronquist 1981, Bogle 1986, Endress 1989) or the Liquidambaroideae (Harms 1930). Shi et al. (2001) noted that Altingia species are evergreen with entire, unlobed leaves; Liquidambar is deciduous with 3-5 or 7-lobed leaves; while Semiliquidambar is evergreen or deciduous, with trilobed, simple or one-lobed leaves. Cytological studies have indicated that the chromosome number of Liquidambar is 2n = 30, 32 (Anderson & Sax 1935, Pizzolongo 1958, Santamour 1972, Goldblatt & Endress 1977). Ferguson (1989) stated that this chromosome number distinguished Liquidambar from the rest of the Hamamelidaceae with their chromosome numbers of 2n = 16, 24, 36, 48, 64 and 72. -
The Phytochemistry of Cherokee Aromatic Medicinal Plants
medicines Review The Phytochemistry of Cherokee Aromatic Medicinal Plants William N. Setzer 1,2 1 Department of Chemistry, University of Alabama in Huntsville, Huntsville, AL 35899, USA; [email protected]; Tel.: +1-256-824-6519 2 Aromatic Plant Research Center, 230 N 1200 E, Suite 102, Lehi, UT 84043, USA Received: 25 October 2018; Accepted: 8 November 2018; Published: 12 November 2018 Abstract: Background: Native Americans have had a rich ethnobotanical heritage for treating diseases, ailments, and injuries. Cherokee traditional medicine has provided numerous aromatic and medicinal plants that not only were used by the Cherokee people, but were also adopted for use by European settlers in North America. Methods: The aim of this review was to examine the Cherokee ethnobotanical literature and the published phytochemical investigations on Cherokee medicinal plants and to correlate phytochemical constituents with traditional uses and biological activities. Results: Several Cherokee medicinal plants are still in use today as herbal medicines, including, for example, yarrow (Achillea millefolium), black cohosh (Cimicifuga racemosa), American ginseng (Panax quinquefolius), and blue skullcap (Scutellaria lateriflora). This review presents a summary of the traditional uses, phytochemical constituents, and biological activities of Cherokee aromatic and medicinal plants. Conclusions: The list is not complete, however, as there is still much work needed in phytochemical investigation and pharmacological evaluation of many traditional herbal medicines. Keywords: Cherokee; Native American; traditional herbal medicine; chemical constituents; pharmacology 1. Introduction Natural products have been an important source of medicinal agents throughout history and modern medicine continues to rely on traditional knowledge for treatment of human maladies [1]. Traditional medicines such as Traditional Chinese Medicine [2], Ayurvedic [3], and medicinal plants from Latin America [4] have proven to be rich resources of biologically active compounds and potential new drugs. -
Full of Beans: a Study on the Alignment of Two Flowering Plants Classification Systems
Full of beans: a study on the alignment of two flowering plants classification systems Yi-Yun Cheng and Bertram Ludäscher School of Information Sciences, University of Illinois at Urbana-Champaign, USA {yiyunyc2,ludaesch}@illinois.edu Abstract. Advancements in technologies such as DNA analysis have given rise to new ways in organizing organisms in biodiversity classification systems. In this paper, we examine the feasibility of aligning two classification systems for flowering plants using a logic-based, Region Connection Calculus (RCC-5) ap- proach. The older “Cronquist system” (1981) classifies plants using their mor- phological features, while the more recent Angiosperm Phylogeny Group IV (APG IV) (2016) system classifies based on many new methods including ge- nome-level analysis. In our approach, we align pairwise concepts X and Y from two taxonomies using five basic set relations: congruence (X=Y), inclusion (X>Y), inverse inclusion (X<Y), overlap (X><Y), and disjointness (X!Y). With some of the RCC-5 relationships among the Fabaceae family (beans family) and the Sapindaceae family (maple family) uncertain, we anticipate that the merging of the two classification systems will lead to numerous merged solutions, so- called possible worlds. Our research demonstrates how logic-based alignment with ambiguities can lead to multiple merged solutions, which would not have been feasible when aligning taxonomies, classifications, or other knowledge or- ganization systems (KOS) manually. We believe that this work can introduce a novel approach for aligning KOS, where merged possible worlds can serve as a minimum viable product for engaging domain experts in the loop. Keywords: taxonomy alignment, KOS alignment, interoperability 1 Introduction With the advent of large-scale technologies and datasets, it has become increasingly difficult to organize information using a stable unitary classification scheme over time. -
Hamamelis Virginiana (Common Witchhazel) Witchhazel Family (Hamamelidaceae)
Hamamelis virginiana (Common Witchhazel) Witchhazel Family (Hamamelidaceae) Introduction: This native large shrub or small tree offers attractive yellow foliage and fragrant fl owers in fall. It is an excellent plant for naturalized settings. Culture: Common witchhazel performs best in moist soils in full sun or shade. It prefers soils that are slightly acidic or neutral, as it is not as tolerant of high pH as Hamamelis vernalis. Common witchhazel is hardy in Zones 3 to 8, possibly 9. Common witchhazel has no serious disease or insect problems, although it may develop galls on the bottom of its leaves if planted near birch trees. Botanical Characteristics: Additional information: The common name witchhazel comes from Native habitat: Canada south to Georgia, west to an old English word that means “to bend.” European Arkansas and Nebraska. species of Hamamelis were once used as divining rods to search for water. Growth habit: Large shrub or small tree with Witchhazel bark has been mixed with water large, spreading branches that form a rounded crown. and alcohol to make an astringent for sores and bruis- es. Tannins found in the bark have also been used to Tree size: 20 to 30 feet tall with a 15- to 20-foot treat hemorrhoids and in eye medications. Witchhazel spread. extract has also been used in after-shave lotion. The bark of witchhazel is light brown and Flower and fruit: Flowers are fragrant and have thin. It peels off to reveal a reddish purple inner bark. four yellow, ribbon-like petals. Flowers are borne Common witchhazel is our native witchhazel in November and are effective for 2 to 4 weeks. -
Witch-Hazel - Wikipedia, the Free Encyclopedia
Witch-hazel - Wikipedia, the free encyclopedia http://en.wikipedia.org/wiki/Witch-hazel You can support Wikipedia by making a tax-deductible donation. Witch-hazel From Wikipedia, the free encyclopedia Witch-hazel (Hamamelis) is a genus of flowering plants in the Witch-hazel family Hamamelidaceae, with two species in North America (H. virginiana and H. vernalis), and one each in Japan (H. japonica) and China (H. mollis). They are deciduous shrubs or (rarely) small trees growing to 3-8 m tall, rarely to 12 m tall. The leaves are alternately arranged, oval, 4-16 cm long and 3-11 cm broad, with a smooth or wavy margin. The horticultural name means "together with fruit"; its fruit, flowers, and next year's leaf buds all appear on the branch simultaneously, a rarity among trees. [1] The flowers are sometimes produced on the leafless stems in winter, thus one alternative name for the plant, "Winterbloom". [1] Each flower has four slender strap-shaped petals 1-2 cm long, pale to dark yellow, orange, or red. The fruit is a two-part capsule 1 cm long, containing a single 5 mm glossy black seed in each of the two parts; the capsule splits explosively at maturity in the autumn about 8 months after flowering, ejecting the seeds with sufficient force to fly for distances of up to 10 m, thus another Hamamelis virginiana alternative name "Snapping Hazel". [1] Scientific classification Kingdom: Plantae Hamamelis species are used as food plants by the larvae of Division: Magnoliophyta some Lepidoptera species including Feathered Thorn. Class: Magnoliopsida The name Witch has its origins in Middle English wiche, from Order: Saxifragales the Old English wice, meaning "pliant" or "bendable". -
Number 3, Spring 1998 Director’S Letter
Planning and planting for a better world Friends of the JC Raulston Arboretum Newsletter Number 3, Spring 1998 Director’s Letter Spring greetings from the JC Raulston Arboretum! This garden- ing season is in full swing, and the Arboretum is the place to be. Emergence is the word! Flowers and foliage are emerging every- where. We had a magnificent late winter and early spring. The Cornus mas ‘Spring Glow’ located in the paradise garden was exquisite this year. The bright yellow flowers are bright and persistent, and the Students from a Wake Tech Community College Photography Class find exfoliating bark and attractive habit plenty to photograph on a February day in the Arboretum. make it a winner. It’s no wonder that JC was so excited about this done soon. Make sure you check of themselves than is expected to seedling selection from the field out many of the special gardens in keep things moving forward. I, for nursery. We are looking to propa- the Arboretum. Our volunteer one, am thankful for each and every gate numerous plants this spring in curators are busy planting and one of them. hopes of getting it into the trade. preparing those gardens for The magnolias were looking another season. Many thanks to all Lastly, when you visit the garden I fantastic until we had three days in our volunteers who work so very would challenge you to find the a row of temperatures in the low hard in the garden. It shows! Euscaphis japonicus. We had a twenties. There was plenty of Another reminder — from April to beautiful seven-foot specimen tree damage to open flowers, but the October, on Sunday’s at 2:00 p.m. -
Abies Concolor (White Fir)
Compiled here is distribution, characteristics and other information on host species featured as ‘Host of the Month’ in past issues of the COMTF Monthly Report. Abies concolor (white fir) This is an evergreen tree native to the mountains of southern Oregon, California, the southern Rocky Mountains, and Baja California. Large and symmetrical, white fir grows 80 – 120ft tall and 15 – 20ft wide in its native range and in the Pacific Northwest. White fir is one of the top timber species found in the Sierra Nevada Mountains of CA and is a popular Christmas tree, as well as one of the most commonly grown native firs in Western gardens. Young trees are conical in shape, but develop a dome-like crown with age. The flattened needles of white fir are silvery blue-green, blunt at the tip , and grow 2 – 3in long. Often curving upwards, the needles extend at right angles from the twig, and twigs produce a citrus smell when needles are broken. White fir is monoecious, producing yellow- to red-toned, catkin-like male flowers and inconspicuous yellow-brown female flowers. The oblong cones grow 3 – 5 in upright, are yellow-green to purple in color, and are deciduous at maturity, dispersing seed in the fall. New twigs are dark- orange, but become gray-green, then gray with maturity. The bark of saplings is thin, smooth, and gray, turning thick, ash-gray with age, and developing deep irregular furrows. P. ramorum- infected Abies concolor (white fir) was first reported in the October 2005 COMTF newsletter as having been found at a Christmas tree farm in the quarantined county of Santa Clara. -
583–584 Angiosperms 583 *Eudicots and Ceratophyllales
583 583 > 583–584 Angiosperms These schedules are extensively revised, having been prepared with little reference to earlier editions. 583 *Eudicots and Ceratophyllales Subdivisions are added for eudicots and Ceratophyllales together, for eudicots alone Class here angiosperms (flowering plants), core eudicots For monocots, basal angiosperms, Chloranthales, magnoliids, see 584 See Manual at 583–585 vs. 600; also at 583–584; also at 583 vs. 582.13 .176 98 Mangrove swamp ecology Number built according to instructions under 583–588 Class here comprehensive works on mangroves For mangroves of a specific order or family, see the order or family, e.g., mangroves of family Combretaceae 583.73 .2 *Ceratophyllales Class here Ceratophyllaceae Class here hornworts > 583.3–583.9 Eudicots Class comprehensive works in 583 .3 *Ranunculales, Sabiaceae, Proteales, Trochodendrales, Buxales .34 *Ranunculales Including Berberidaceae, Eupteleaceae, Menispermaceae, Ranunculaceae Including aconites, anemones, barberries, buttercups, Christmas roses, clematises, columbines, delphiniums, hellebores, larkspurs, lesser celandine, mandrake, mayapple, mayflower, monkshoods, moonseeds, wolfsbanes For Fumariaceae, Papaveraceae, Pteridophyllaceae, see 583.35 See also 583.9593 for mandrakes of family Solanaceae .35 *Fumariaceae, Papaveraceae, Pteridophyllaceae Including bleeding hearts, bloodroot, celandines, Dutchman’s breeches, fumitories, poppies See also 583.34 for lesser celandine .37 *Sabiaceae * *Add as instructed under 583–588 1 583 Dewey Decimal Classification