Selecting Firewise Shrubs to Reduce Wildfire Risk
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												  Central Appalachian Broadleaf Forest Coniferous Forest Meadow ProvinceSelecting Plants for Pollinators A Regional Guide for Farmers, Land Managers, and Gardeners In the Central Appalachian Broadleaf Forest Coniferous Forest Meadow Province Including the states of: Maryland, Pennsylvania, Virginia, West Virginia And parts of: Georgia, Kentucky, and North Carolina, NAPPC South Carolina, Tennessee Table of CONTENTS Why Support Pollinators? 4 Getting Started 5 Central Appalachian Broadleaf Forest 6 Meet the Pollinators 8 Plant Traits 10 Developing Plantings 12 Far ms 13 Public Lands 14 Home Landscapes 15 Bloom Periods 16 Plants That Attract Pollinators 18 Habitat Hints 20 This is one of several guides for Check list 22 different regions in the United States. We welcome your feedback to assist us in making the future Resources and Feedback 23 guides useful. Please contact us at [email protected] Cover: silver spotted skipper courtesy www.dangphoto.net 2 Selecting Plants for Pollinators Selecting Plants for Pollinators A Regional Guide for Farmers, Land Managers, and Gardeners In the Ecological Region of the Central Appalachian Broadleaf Forest Coniferous Forest Meadow Province Including the states of: Maryland, Pennsylvania, Virginia, West Virginia And parts of: Georgia, Kentucky, North Carolina, South Carolina, Tennessee a nappc and Pollinator Partnership™ Publication This guide was funded by the National Fish and Wildlife Foundation, the C.S. Fund, the Plant Conservation Alliance, the U.S. Forest Service, and the Bureau of Land Management with oversight by the Pollinator Partnership™ (www.pollinator.org), in support of the North American Pollinator Protection Campaign (NAPPC–www.nappc.org). Central Appalachian Broadleaf Forest – Coniferous Forest – Meadow Province 3 Why support pollinators? In theIr 1996 book, the Forgotten PollInators, Buchmann and Nabhan estimated that animal pollinators are needed for the reproduction “ Farming feeds of 90% of flowering plants and one third of human food crops.
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												  Nerium Oleander Linn. (Kaner)Available online on www.ijppr.com International Journal of Pharmacognosy and Phytochemical Research 2014; 6(3): 593-597 ISSN: 0975-4873 Review Article A Review on: Nerium oleander Linn. (Kaner) *Chaudhary Kiran1, Prasad D.N.2 1K.C. Institute of Pharmaceutical Sciences, Pandoga, Distt.Una (H.P.) 2Shivalik College of Pharmacy, Naya Nangal, Distt.Ropar, Punjab Available Online: 1st September 2014 ABSTRACT Nerium oleander is an evergreen shrub or small tree in the dogbane family Apocyanaceae. It is commonly known as oleander but has many other names like Nerium indicum mill. and Nerium odorum soland. It bears flowers in clusters with white, pink, yellow and red colours. It contains plumericin, alpha-amyrin, beta-sitosterol, kaempferol, cardioactive glycosides named Odorosides A-H obtained from the root bark. Leaves contain the cardiac glycosides kaneroside, neriumoside, digitoxigenin, alpha –L-olendroside -5α-adynerin and other glycosides. Odorosides are cardioactive glycosides. Gentiobiosyl –oleandrin, Odoroside A and Oleandrin were the main glycosides identified. It has potent cardiotonic activity, digitalis like effect on heart. It has been reported to have effective against skin diseases,wound infections, cancer, diabetes, inflammation and CNS depression. All parts of the plant are poisonous in nature which can be treated by the use of activated charcoal.Topical preparation containing Nerium extract can be used as antiageing cream. Keywords : Nerium oleander, Nerium indicum, Oleander, Cardiotonic, Odorosides , Antibacterial, Antiageing INTRODUCTION Nepal westwards to Kashmir upto 1950m, extending to Taxonomic classification Baluchistan, Afghanistan and found throughout India in Phyllum- Plantae gardens .The white and red flowered variety is equated Class/ Subphyllum- Angiosperms with Nerium indicum.
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												  Native Trees of Georgia1 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.
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												  Native Plants for Conservation, Restoration & LandscapingABOUT THE NATIVE PLANTS FOR CONSERVATION, WHAT ARE NATIVES? For more information, refer to field guides and publications RESTORATION AND LANDSCAPING PROJECT Native species evolved within specific regions and dispersed on local natural history for color, shape, height, bloom times This project is a collaboration between the Virginia Depart- throughout their range without known human involvement. and specific wildlife value of the plants that grow in your ment of Conservation and Recreation and the Virginia Native They form the primary component of the living landscape region. Visit a nearby park, natural area preserve, forest or Plant Society. VNPS chapters across the state helped to fund and provide food and shelter for wildlife management area to learn about common plant the 2011 update to this brochure. native animal species. Native associations, spatial groupings and habitat conditions. For The following partners have provided valuable assistance plants co-evolved with specific recommendations and advice about project design, throughout the life of this project: native animals over many consult a landscape or garden design specialist with thousands to millions of experience in native plants. TheNatureConservancy–VirginiaChapter•Virginia years and have formed TechDepartmentofHorticulture•VirginiaDepartmentof complex and interdependent WHAT ARE NON-NATIVE PLANTS? AgricultureandConsumerServices•VirginiaDepartment relationships. Our native Sometimes referred to as “exotic,” “alien,” or “non- of Environmental Quality, Coastal Zone Management fauna depend on native indigenous,” non-native plants are species introduced, Program•VirginiaDepartmentofForestry•Virginia flora to provide food and DepartmentofGameandInlandFisheries•Virginia Native intentionally or accidentally, into a new region by cover.
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												  State of New York City's Plants 2018STATE 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.
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												  RHODODENDRON STATE PARK Soils, It Can Spread to Surrounding Upland AreasDIRECTIONS GIANT RHODODENDRON NH Natural Heritage Bureau From Rte. 119 between Fitzwilliam and Richmond, Giant rhododendron (Rhododendron maximum), take Rhododendron Rd and follow signs to the park. also known as great laurel or rosebay, is a large ev- Visiting New Hampshire’s Biodiversity ergreen shrub known for its showy flower displays. It is near the northern limit of its range in New Rhododendron Hampshire and native populations are rare. In fact, it is considered rare or uncommon throughout New State Park England. It is really a species of the southern and central Appalachians, where it is common on wooded mountain slopes, often forming dense and extensive colonies. Giant rhododendron prefers moist acidic soils that are high in organic matter, like those found in ever- green swamps. However, once established in moist RHODODENDRON STATE PARK soils, it can spread to surrounding upland areas. In addition to producing seed, rhododendron can This 2,723-acre park located in southwestern NH is spread vegetatively through a process called named after its focal point, a 16-acre grove of giant “layering,” where low growing branches that make rhododendron. A universally accessible trail encir- contact with the soil can take root, establishing new cles the grove allowing visitors to observe the plants stems and expanding the colony. close up. Mid-July is the best time to see blooms. The fragrant clusters of the giant rhododendron’s PARK USE GUIDELINES pink and white blossoms burst into bloom in mid- This park is open to the public for recreation and July and often last for a few weeks.
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												  Rosebay Rhododendron Rhododendron MaximumSUMMER 2004, VOLUME 5, ISSUE 3 NEWSLETTER OF THE NORTH AMERICAN NATIVE PLANT SOCIETY Native Plant to Know Rosebay rhododendron Rhododendron maximum by Kevin Kavanagh Joyce Kilmer Memorial Forest, tucked away inside the Nantahala National Forest RANTON of North Carolina’s Appalachian G Mountains, is one of those RIGITTE North American pil- B grimages that all botanists should make at least once in ILLUSTRATION BY their lives.As a graduate student in for- est ecology, I had read about it in the scientific literature, one of the best examples of an old-growth ‘cove’ forest on the continent: massive tulip trees (Lirio- dendron tulipifera) more than 500 years old, east- ern hemlocks (Tsuga canadensis) rivalling their large elliptic leaves forming a delicate pat- Appalachian chain.Although hardy in eastern their west-coast tern against the bright yellows of overstorey Canadian gardens, Rhododendron maximum rainforest cousins tulip trees in peak autumn coloration.Along does not penetrate naturally into Canada. in size and age, mountain streams, the trails wove in among While there are historical accounts from and, along the expansive rhododendron thickets that in Ontario, Quebec, New Brunswick and Nova streams, dense under- places rose more than 10 metres (30 feet) over- Scotia, none of them, to my knowledge, have storey stands of rosebay rhododendrons head on gnarled stems (trunks!), the largest of been authenticated. (Rhododendron maximum) forming a dark which were close to 30 centimetres (one foot) In its native range, rosebay rhododendron canopy overhead. in diameter. (also known as great-laurel or great rhododen- To call it a canopy is not embellishment.
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												  A Dunedin GardenVIREYA VINE ISSUE #82, OCTOBER 2007 PUBLISHED BY THE EDUCATION COMMITTEE OF THE RHODODENDRON SPECIES FOUNDATION R.S.F. PO BOX 3798, FEDERAL WAY, WA. 98063 E. White Smith, Editor From Daphne and Gavin Clark Dunedin, New Zealand Published with permission from the Dunedin Bulletin Feb. 2007 RHODODENDRON lowii (Subsection Vireya) More information about R. lowii relting to the piece in VV81 Addendum – February 2007 Following on from the previous article the long cane produced four shoots. Two were given to a very keen propagator to strike and we tried to strike two, but they all failed. However a good quantity of seed was collected at the end of January, 2005 and again this was shared. Our seed was kept in cool storage and eventually sown in September 2005. A small transparent plastic container with a clear lid was used with the seed sprinkled on to damp, sterilized sphagnum moss. The seeds germinated very well and some of the seedlings were transferred into compost but despite tender care died. The remaining seedlings stayed in the plastic container for some considerable time until recently when they were very carefully removed to individual peat pots into a specially mixed compost. Nine pots are housed in a clear, plastic lidded container 340mm x 300mm which stands on a wide kitchen windowsill with excellent light but no direct sunlight and hopefully some of these will survive. In the meantime the parent plant is flourishing, the two basal shoots are now 800mm high with the original cane cut down to 750mm. It is still in its container and now occupies a choice place among other vireya species in a wooded area beneath 50 year old camellias and rhododendrons which have been pruned to provide an excellent canopy, with morning sun, filtered afternoon sunlight, together with a degree of humidity.
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												  European Academic ResearchEUROPEAN ACADEMIC RESEARCH Vol. IV, Issue 10/ January 2017 Impact Factor: 3.4546 (UIF) ISSN 2286-4822 DRJI Value: 5.9 (B+) www.euacademic.org Evidences from morphological investigations supporting APGIII and APGIV Classification of the family Apocynaceae Juss., nom. cons IKRAM MADANI Department of Botany, Faculty of Science University of Khartoum, Sudan LAYALY IBRAHIM ALI Faculty of Science, University Shandi EL BUSHRA EL SHEIKH EL NUR Department of Botany, Faculty of Science University of Khartoum, Sudan Abstract: Apocynaceae have traditionally been divided into into two subfamilies, the Plumerioideae and the Apocynoideae. Recently, based on molecular data, classification of Apocynaceae has undergone considerable revisions. According to the Angiosperm Phylogeny Group III (APGIII, 2009), and the update of the Angiosperm Phylogeny Group APG (APGIV, 2016) the family Asclepiadaceae is now included in the Apocynaceae. The family, as currently recognized, includes some 1500 species divided in about 424 genera and five subfamilies: Apocynoideae, Rauvolfioideae, Asclepiadoideae, Periplocoideae, and Secamonoideae. In this research selected species from the previous families Asclepiadaceae and Apocynaceae were morphologically investigated in an attempt to distinguish morphological important characters supporting their new molecular classification. 40 morphological characters were treated as variables and analyzed for cluster of average linkage between groups using the statistical package SPSS 16.0. Resulting dendrograms confirm the relationships between species from the previous families on the basis of their flowers, fruits, 8259 Ikram Madani, Layaly Ibrahim Ali, El Bushra El Sheikh El Nur- Evidences from morphological investigations supporting APGIII and APGIV. Classification of the family Apocynaceae Juss., nom. cons and seeds morphology. Close relationships were reported between species from the same subfamilies.
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												  A Hydroalcoholic Extract from the Leaves of Nerium Oleander Inhibits Glycolysis and Induces Selective Killing of Lung Cancer CellsOriginal Papers A Hydroalcoholic Extract from the Leaves of Nerium oleander Inhibits Glycolysis and Induces Selective Killing of Lung Cancer Cells Authors José Manuel Calderón-Montaño1, Estefanía Burgos-Morón1, Manuel Luis Orta2, Santiago Mateos2, Miguel López-Lázaro1 Affiliations 1 Department of Pharmacology, Faculty of Pharmacy, University of Seville, Seville, Spain 2 Department of Cell Biology, Faculty of Biology, University of Seville, Seville, Spain Key words Abstract consumption and lactate production) in A549 l" Nerium oleander ! cells, comparable to that of the glycolysis inhibitor l" Apocynaceae Recent evidence suggests that cardiac glycosides dichloroacetate (currently in clinical develop- l" cardiac glycosides might be used for the treatment of cancer. The or- ment for cancer therapy). Because platinum com- l" cardiotonic steroids namental shrub Nerium oleander has been used in pounds are widely used in the treatment of lung l" anticancer traditional medicine for treating several disorders cancer, we tested the cytotoxicity of several com- including cancer, and extracts from the leaves of binations of cisplatin with the extract and found a this plant have already entered phase I clinical tri- moderate synergism when Nerium oleander ex- als. In this communication, we have prepared a tract was administered after cisplatin but a mod- hydroalcoholic extract from the leaves of Nerium erate antagonism when it was added before cis- oleander (containing 4.75 ± 0.32% of cardenolides) platin. Our results suggest that extracts from Ne- and have assessed its cytotoxic activity in A549 rium oleander might induce anticancer effects in lung cancer cells vs. MRC5 nonmalignant lung fi- patients with lung cancer and support their possi- broblasts.
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												  Introduction to the Southern Blue Ridge Ecoregional Conservation PlanSOUTHERN BLUE RIDGE ECOREGIONAL CONSERVATION PLAN Summary and Implementation Document March 2000 THE NATURE CONSERVANCY and the SOUTHERN APPALACHIAN FOREST COALITION Southern Blue Ridge Ecoregional Conservation Plan Summary and Implementation Document Citation: The Nature Conservancy and Southern Appalachian Forest Coalition. 2000. Southern Blue Ridge Ecoregional Conservation Plan: Summary and Implementation Document. The Nature Conservancy: Durham, North Carolina. This document was produced in partnership by the following three conservation organizations: The Nature Conservancy is a nonprofit conservation organization with the mission to preserve plants, animals and natural communities that represent the diversity of life on Earth by protecting the lands and waters they need to survive. The Southern Appalachian Forest Coalition is a nonprofit organization that works to preserve, protect, and pass on the irreplaceable heritage of the region’s National Forests and mountain landscapes. The Association for Biodiversity Information is an organization dedicated to providing information for protecting the diversity of life on Earth. ABI is an independent nonprofit organization created in collaboration with the Network of Natural Heritage Programs and Conservation Data Centers and The Nature Conservancy, and is a leading source of reliable information on species and ecosystems for use in conservation and land use planning. Photocredits: Robert D. Sutter, The Nature Conservancy EXECUTIVE SUMMARY This first iteration of an ecoregional plan for the Southern Blue Ridge is a compendium of hypotheses on how to conserve species nearest extinction, rare and common natural communities and the rich and diverse biodiversity in the ecoregion. The plan identifies a portfolio of sites that is a vision for conservation action, enabling practitioners to set priorities among sites and develop site-specific and multi-site conservation strategies.
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												  D.1A Floral and Faunal CompendiaAppendix D.1a Floral and Faunal Compendia APPENDIX D.1a FLORAL AND FAUNAL COMPENDIA INTRODUCTION TO FLORAL AND FAUNAL SURVEY Expected site use by wildlife is derived from survey information combined with documented habitat preferences of regional wildlife species, which, whether or not recorded during the survey, are considered likely to include the project area within their range. Habitat designations used in this report are according to the classification system of Holland (1986). Floral taxonomy used in this report follows the Jepson Manual (Hickman 1993), with updates in accordance to the online Jepson Interchange where known. Common plant names, where not available from Munz (1974), are taken from Abrams (1923), Robbins, et al. (1951), Collins (1972), Niehaus and Ripper (1976) and Muns (1983). Vertebrates identified in the field by sight, calls, tracks, scat or other signs are cited according to the nomenclature of Jennings (1983) for amphibians and reptiles; AOU (1983) for birds; and Jones, et al. (1982) for mammals. Butterflies observed or collected in the field were identified with the help of Garth and Tilden (1986) and Tilden and Smith (1986). FLORAL COMPENDIUM1 LEGEND * Nonnative @ Ornamental/Landscape VASCULAR PLANTS CONIFERAE PINACEAE - PINE FAMILY * Pinus halepensis Aleppo Pine ANGIOSPERMAE (DICOTYLEDONS) ANACARDIACEAE - SUMAC FAMILY Malosma laurina laurel sumac Rhus ovata sugar bush * Schinus molle Peruvian pepper-tree Toxicodendron diversilobum poison-oak APOCYNACEAE - DOGBANE FAMILY * Vinca major periwinkle * Nerium oleander oleander ASTERACEAE - SUNFLOWER FAMILY Baccharis pilularis coyote brush Baccharis salicifolia mulefat Helianthus gracilentus slender sunflower * Picris echioides bristly ox-tongue * Silybum marianum milk thistle * Sonchus asper prickly sow-thistle * Sonchus oleraceus common sow-thistle Stephanomeria virgata twiggy wreathplant BRASSICACEAE - MUSTARD FAMILY * Brassica nigra black mustard * Sisymbrium officinale hedge-mustard CAPRIFOLIACEAE - HONEYSUCKLE FAMILY Sambuccus.