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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 -
Plum Crazy: Rediscovering Our Lost Prunus Resources W.R
Plum Crazy: Rediscovering Our Lost Prunus Resources W.R. Okie1 U.S. Department of Agriculture–Agricultural Research Service, Southeastern Fruit and Tree Nut Research Laboratory, 21 Dunbar Road, Byron, GA 31008 Recent utilization of genetic resources of peach [Prunus persica (‘Quetta’ from India, ‘John Rivers’ from England, and ‘Lippiatts’ (L.) Batsch] and Japanese plum (P. salicina Lindl. and hybrids) has from New Zealand) were critical to the development of modern been limited in the United States compared with that of many crops. nectarines in California (Taylor, 1959). However, most fresh-market Difficulties in collection, importation, and quarantine throughput have peach breeding programs in the United States have used germplasm limited the germplasm available. Prunus is more difficult to preserve developed in the United States for cultivar development (Okie, 1998). because more space is needed than for small fruit crops, and the shorter Only in New Jersey was there extensive hybridization with imported life of trees relative to other tree crops because of disease and insect clones, and most of these hybrids have not resulted in named cultivars problems. Lack of suitable rootstocks has also reduced tree life. The (Blake and Edgerton, 1946). trend toward fewer breeding programs, most of which emphasize In recent years, interest in collecting and utilizing novel germplasm “short-term” (long-term compared to most crops) commercial cultivar has increased. For example, non-melting clingstone peaches from development to meet immediate industry needs, has also contributed Mexico and Brazil have been used in the joint USDA–Univ. of to reduced use of exotic material. Georgia–Univ. of Florida breeding program for the development of Probably all modern commercial peaches grown in the United early ripening, non-melting, fresh-market peaches for low-chill areas States are related to ‘Chinese Cling’, a peach imported from China (Beckman and Sherman, 1996). -
Taxon Order Family Scientific Name Common Name Non-Native No. of Individuals/Abundance Notes Bees Hymenoptera Andrenidae Calliop
Taxon Order Family Scientific Name Common Name Non-native No. of individuals/abundance Notes Bees Hymenoptera Andrenidae Calliopsis andreniformis Mining bee 5 Bees Hymenoptera Apidae Apis millifera European honey bee X 20 Bees Hymenoptera Apidae Bombus griseocollis Brown belted bumble bee 1 Bees Hymenoptera Apidae Bombus impatiens Common eastern bumble bee 12 Bees Hymenoptera Apidae Ceratina calcarata Small carpenter bee 9 Bees Hymenoptera Apidae Ceratina mikmaqi Small carpenter bee 4 Bees Hymenoptera Apidae Ceratina strenua Small carpenter bee 10 Bees Hymenoptera Apidae Melissodes druriella Small carpenter bee 6 Bees Hymenoptera Apidae Xylocopa virginica Eastern carpenter bee 1 Bees Hymenoptera Colletidae Hylaeus affinis masked face bee 6 Bees Hymenoptera Colletidae Hylaeus mesillae masked face bee 3 Bees Hymenoptera Colletidae Hylaeus modestus masked face bee 2 Bees Hymenoptera Halictidae Agapostemon virescens Sweat bee 7 Bees Hymenoptera Halictidae Augochlora pura Sweat bee 1 Bees Hymenoptera Halictidae Augochloropsis metallica metallica Sweat bee 2 Bees Hymenoptera Halictidae Halictus confusus Sweat bee 7 Bees Hymenoptera Halictidae Halictus ligatus Sweat bee 2 Bees Hymenoptera Halictidae Lasioglossum anomalum Sweat bee 1 Bees Hymenoptera Halictidae Lasioglossum ellissiae Sweat bee 1 Bees Hymenoptera Halictidae Lasioglossum laevissimum Sweat bee 1 Bees Hymenoptera Halictidae Lasioglossum platyparium Cuckoo sweat bee 1 Bees Hymenoptera Halictidae Lasioglossum versatum Sweat bee 6 Beetles Coleoptera Carabidae Agonum sp. A ground beetle -
(Prunus Spp) Using Random Amplified Microsatellite Polymorphism Markers
Assessment of genetic diversity and relationships among wild and cultivated Tunisian plums (Prunus spp) using random amplified microsatellite polymorphism markers H. Ben Tamarzizt, S. Ben Mustapha, G. Baraket, D. Abdallah and A. Salhi-Hannachi Laboratory of Molecular Genetics, Immunology & Biotechnology, Faculty of Sciences of Tunis, University of Tunis El Manar, El Manar, Tunis, Tunisia Corresponding author: A. Salhi-Hannachi E-mail: [email protected] Genet. Mol. Res. 14 (1): 1942-1956 (2015) Received January 8, 2014 Accepted July 8, 2014 Published March 20, 2015 DOI http://dx.doi.org/10.4238/2015.March.20.4 ABSTRACT. The usefulness of random amplified microsatellite polymorphism markers to study the genetic diversity and relationships among cultivars belonging to Prunus salicina and P. domestica and their wild relatives (P. insititia and P. spinosa) was investigated. A total of 226 of 234 bands were polymorphic (96.58%). The 226 random amplified microsatellite polymorphism markers were screened using 15 random amplified polymorphic DNA and inter-simple sequence repeat primers combinations for 54 Tunisian plum accessions. The percentage of polymorphic bands (96.58%), the resolving power of primers values (135.70), and the polymorphic information content demonstrated the efficiency of the primers used in this study. The genetic distances between accessions ranged from 0.18 to 0.79 with a mean of 0.24, suggesting a high level of genetic diversity at the intra- and interspecific levels. The unweighted pair group with arithmetic mean dendrogram Genetics and Molecular Research 14 (1): 1942-1956 (2015) ©FUNPEC-RP www.funpecrp.com.br Genetic diversity of Tunisian plums using RAMPO markers 1943 and principal component analysis discriminated cultivars efficiently and illustrated relationships and divergence between spontaneous, locally cultivated, and introduced plum types. -
The Importance of Geographic and Biological Variables in Predicting
Horticulture Publications Horticulture 6-2013 The mpI ortance of Geographic and Biological Variables in Predicting the Naturalization of Non- Native Woody Plants in the Upper Midwest Mark P. Widrlechner Iowa State University, [email protected] Emily J. Kapler Iowa State University, [email protected] Philip M. Dixon Iowa State University, [email protected] Janette R. Thompson Iowa State University, [email protected] Follow this and additional works at: https://lib.dr.iastate.edu/hort_pubs Part of the Ecology and Evolutionary Biology Commons, Forest Management Commons, Horticulture Commons, and the Statistical Models Commons The ompc lete bibliographic information for this item can be found at https://lib.dr.iastate.edu/ hort_pubs/33. For information on how to cite this item, please visit http://lib.dr.iastate.edu/ howtocite.html. This Article is brought to you for free and open access by the Horticulture at Iowa State University Digital Repository. It has been accepted for inclusion in Horticulture Publications by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. The mpI ortance of Geographic and Biological Variables in Predicting the Naturalization of Non-Native Woody Plants in the Upper Midwest Abstract The es lection, introduction, and cultivation of non-native woody plants beyond their native ranges can have great benefits, but also unintended consequences. Among these consequences is the tendency for some species to naturalize and become invasive pests in new environments to which they were introduced. In lieu of lengthy and costly field trials, risk-assessment models can be used to predict the likelihood of naturalization. -
Major Indicator Shrubs and Herbs in Riparian Zones on National Forests of Central Oregon
United States Department of Major Indicator Shrubs and Agriculture Herbs in Riparian Zones on Forest Service National Forests of Pacific Northwest Central Oregon. Region by Bernard L. Kovaichik William E. Hopkins and Steven J. Brunsfeld Major Indicator Shrubs and Herbs in Riparian Zones on National Forests of Central Oregon By Bernard L. Kovaichik, Area IV Riparian Ecologist William E. Hopkins, Area IV Area Ecologist and Steven J. Brunsfeld, University of Idaho June, 1988 1988 USDA - Forest Service Pacific Northwest Region R6-ECOL-TP-005-88 I Acknowledgements: The authors wish to thank all those who kindlydonated their time to this publication. Thanks to Bill Hopkins and Rob Rawlings for blazingthe trail with their "Major indicator shrubs and herbson National Forests in eastern Oregon" (Hopkins and Rawlings, 1985). They developedthe format for this style of guide."Major indicator shrubs and herbs on National Forests of western Oregon and southwestern Washington"(Halverson and others, 1986) follows a similar format andwas another resource for developing this guide. Thanks to Carl Burke for illustrating some of thesketches in the glossary and Nancy Halverson, Linda Newman and Nancy Shaw forediting the document.Thanks to David Mattson for his sketch of eastwood willow. Photo credits: Bernard L. Kovalchik Steven J. Brunsfeld Wayne D. Padgett Line drawings used by permission from: Hitchcock, C. L., A. Cronquist, M. Ownberg and J. W. Thompson.1977. Vascular plants of the Pacific Northwest. Vol. 1-5. Univ. of Washington Press. Seattle. 2978p. Brunsfeld, S. J. and F. D. Johnson. 1985. Field guide to thewillows of east-central Idaho. Forest, Wildlife, and Range Experiment Station Bull. -
State of New York City's Plants 2018
STATE OF NEW YORK CITY’S PLANTS 2018 Daniel Atha & Brian Boom © 2018 The New York Botanical Garden All rights reserved ISBN 978-0-89327-955-4 Center for Conservation Strategy The New York Botanical Garden 2900 Southern Boulevard Bronx, NY 10458 All photos NYBG staff Citation: Atha, D. and B. Boom. 2018. State of New York City’s Plants 2018. Center for Conservation Strategy. The New York Botanical Garden, Bronx, NY. 132 pp. STATE OF NEW YORK CITY’S PLANTS 2018 4 EXECUTIVE SUMMARY 6 INTRODUCTION 10 DOCUMENTING THE CITY’S PLANTS 10 The Flora of New York City 11 Rare Species 14 Focus on Specific Area 16 Botanical Spectacle: Summer Snow 18 CITIZEN SCIENCE 20 THREATS TO THE CITY’S PLANTS 24 NEW YORK STATE PROHIBITED AND REGULATED INVASIVE SPECIES FOUND IN NEW YORK CITY 26 LOOKING AHEAD 27 CONTRIBUTORS AND ACKNOWLEGMENTS 30 LITERATURE CITED 31 APPENDIX Checklist of the Spontaneous Vascular Plants of New York City 32 Ferns and Fern Allies 35 Gymnosperms 36 Nymphaeales and Magnoliids 37 Monocots 67 Dicots 3 EXECUTIVE SUMMARY This report, State of New York City’s Plants 2018, is the first rankings of rare, threatened, endangered, and extinct species of what is envisioned by the Center for Conservation Strategy known from New York City, and based on this compilation of The New York Botanical Garden as annual updates thirteen percent of the City’s flora is imperiled or extinct in New summarizing the status of the spontaneous plant species of the York City. five boroughs of New York City. This year’s report deals with the City’s vascular plants (ferns and fern allies, gymnosperms, We have begun the process of assessing conservation status and flowering plants), but in the future it is planned to phase in at the local level for all species. -
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. -
2010 the Michigan Botanist 73
2010 THE MICHIGAN BOTANIST 73 NOMENCLATURE OF THE THICKET CREEPER, PARTHENOCISSUS INSERTA (VITACEAE) James S. Pringle Royal Botanical Gardens P.O. Box 399 Hamilton, Ontario, Canada L8N 3H8 ABSTRACT Parthenocissus inserta (A. Kern.) Fritsch, rather than P. vitacea (Knerr) Hitchc., is the correct name for the thicket creeper, a species related to the Virginia creeper, P. quinquefolia . KEY WORDS: Parthenocissus , Vitaceae Two species of Parthenocissus are native to eastern and central North Amer - ica. One of these, to which the common name Virginia creeper is more appropri - ately applied, is P. quinquefolia (L.) Planch. Its natural range extends from Mex - ico probably to southern Maine, southern Ontario, and southern Minnesota, although it has escaped from cultivation farther north. The other species, the nomenclature of which is discussed here, has a more northern and western range, from Pennsylvania, Texas, and California north to ca. 50°N in Ontario and Man - itoba. “False Virginia creeper,” “thicket creeper,” and “grape-woodbine” have been proposed as vernacular names for the northern species, but none of these names has become widely used. Because of their abundance and the size of the plants, these species are ecologically important, influencing succession and pro - viding cover and food for wildlife. They are widely cultivated as ornamental vines in North America and Europe, although they may sometimes become a problem, as when shrubs or specimen trees are engulfed. Until early in the twentieth century few botanists distinguished between these species, and the assumption that “the” Virginia creeper is Parthenocissus quin - quefolia continues to result in reports of P. quinquefolia from localities north of its true range. -
Amur Maple Acer Ginnala Maxim., Syn Acer Tataricum Ssp
MN NWAC Risk Common Name Latin Name Assessment Worksheet (04-2011) Amur maple Acer ginnala Maxim., syn Acer tataricum ssp. ginnala Reviewer Affiliation/Organization Date (mm/dd/yyyy) Laura Van Riper, MN Department of Natural Resources, 09/17/2015 Tim Power MN Nursery and Landscape Association Box Question Answer Outcome 1 Is the plant species or genotype non-native? Yes. Amur maple is native to Asia. Go to Box 3 3 Is the plant species, or a related species, Yes. Go to Box 6 documented as being a problem elsewhere? Regulated as a Restricted Invasive Species In Wisconsin (all cultivars exempt) (http://dnr.wi.gov/topic/Invasives/fact/AmurMaple.html). Ranked as moderately invasive in New York (http://www.nyis.info/user_uploads/4a6d0_1db2a_Acer.g innala.NYS.pdf). Listed on Illinois Departments of Natural Resources Exotic Species webpages (http://dnr.state.il.us/education/exoticspecies/amurmaple. htm). NatureServe I rank of Medium/Insignificant (http://explorer.natureserve.org/servlet/NatureServe?sear chName=Acer+ginnala). Listed as potentially invasive, but not banned in Connecticut (http://plants.usda.gov/java/noxious?rptType=State&stat efips=09, http://cipwg.uconn.edu/invasive_plant_list/). 6 Does the plant species have the capacity to Yes. Go to Box 7 establish and survive in Minnesota? 1 Box Question Answer Outcome A. Is the plant, or a close relative, currently Yes. Go to Box 7 established in Minnesota? Amur maple has been widely planted in Minnesota. EDDMaps reports Amur maple as present in 42 counties in Minnesota, especially in the northeastern part of the state (http://eddmaps.org/distribution/uscounty.cfm?sub=3965 ). -
Appendix 2: Plant Lists
Appendix 2: Plant Lists Master List and Section Lists Mahlon Dickerson Reservation Botanical Survey and Stewardship Assessment Wild Ridge Plants, LLC 2015 2015 MASTER PLANT LIST MAHLON DICKERSON RESERVATION SCIENTIFIC NAME NATIVENESS S-RANK CC PLANT HABIT # OF SECTIONS Acalypha rhomboidea Native 1 Forb 9 Acer palmatum Invasive 0 Tree 1 Acer pensylvanicum Native 7 Tree 2 Acer platanoides Invasive 0 Tree 4 Acer rubrum Native 3 Tree 27 Acer saccharum Native 5 Tree 24 Achillea millefolium Native 0 Forb 18 Acorus calamus Alien 0 Forb 1 Actaea pachypoda Native 5 Forb 10 Adiantum pedatum Native 7 Fern 7 Ageratina altissima v. altissima Native 3 Forb 23 Agrimonia gryposepala Native 4 Forb 4 Agrostis canina Alien 0 Graminoid 2 Agrostis gigantea Alien 0 Graminoid 8 Agrostis hyemalis Native 2 Graminoid 3 Agrostis perennans Native 5 Graminoid 18 Agrostis stolonifera Invasive 0 Graminoid 3 Ailanthus altissima Invasive 0 Tree 8 Ajuga reptans Invasive 0 Forb 3 Alisma subcordatum Native 3 Forb 3 Alliaria petiolata Invasive 0 Forb 17 Allium tricoccum Native 8 Forb 3 Allium vineale Alien 0 Forb 2 Alnus incana ssp rugosa Native 6 Shrub 5 Alnus serrulata Native 4 Shrub 3 Ambrosia artemisiifolia Native 0 Forb 14 Amelanchier arborea Native 7 Tree 26 Amphicarpaea bracteata Native 4 Vine, herbaceous 18 2015 MASTER PLANT LIST MAHLON DICKERSON RESERVATION SCIENTIFIC NAME NATIVENESS S-RANK CC PLANT HABIT # OF SECTIONS Anagallis arvensis Alien 0 Forb 4 Anaphalis margaritacea Native 2 Forb 3 Andropogon gerardii Native 4 Graminoid 1 Andropogon virginicus Native 2 Graminoid 1 Anemone americana Native 9 Forb 6 Anemone quinquefolia Native 7 Forb 13 Anemone virginiana Native 4 Forb 5 Antennaria neglecta Native 2 Forb 2 Antennaria neodioica ssp. -
SHRUBS Almond Russian ‘Regal’ (Prunus Tenella ‘Regal’ ) NRCS Selection
TREE DESCRIPTIONS Big Sioux Nursery, Inc. 16613 Sioux Conifer Road Watertown, SD 57201 1-605-886-6806 1-800-968-6806 E-Mail: [email protected] SHRUBS Almond Russian ‘Regal’ (Prunus tenella ‘Regal’ ) NRCS selection. Introduced from Europe and Asia. Suckers to form small colony. Produces showy pink or white flowers and a hairy inedible fruit. Can tolerate heavy clay and gumbo soils. Doesn’t tolerate waterlogged soil. (Size: 6/32, 12-20”) Aronia 'McKenzie' (Aronia melanocarpa) NRCS Selection. Attractive white flowers, glossy foliage, and black berries. Edible fruit attracts birds. Excellent fall color. (Size 6/32”, 12-20”) Buffaloberry (Shepherdia argentea Native. Suckers to form colony. High pH and drought tolerant. Attractive silver leaves. Red fruit can be used for jelly. Good for wildlife. (Size: 6/32”, 12-20”) Caragana (Caragana arborescens) Introduced from Siberia and Manchuria. Sometimes called pea shrub. Produces yellow flowers in spring. Non-edible seedpods. Fine-leafed. High pH and drought tolerant. Extremely hardy and long lived. (Size: 6/32”, 12-20”) Cherry, Mongolian (Prunus fruticosa) Introduced from Eastern Europe, Asia, Siberia, and Mongolia. Suckers slowly to form a colony. Glossy leaves. Showy white flowers and tart red fruit. Excellent for jelly. (Size: 5/32”, 12-20”) Cherry, Nanking (Prunus tomentosa) Introduced from China and Japan. Showy flowers and sweet red fruit. Good for jelly. Plants may be renewed by cutting to ground. Good for wildlife. (Size: 5/32”, 12-20”) Cherry, Sand (Prunus besseyi) Native. Glossy silver-green leaves. Suckers slightly to produce a low thicket. White flowers in spring and purple fruit in summer.