Influence of Silvicultural Treatment, Site Characteristics, and Land Use
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Rosa Canina Linnaeus Common Names: Dog Rose, Dog Brier, Wild Rose (5,6,13)
Rosa canina Linnaeus Common Names: Dog rose, dog brier, wild rose (5,6,13). Etymology: ‘Rosa’ is the Latin word for ‘rose’, and ‘canina’ in Latin means ‘of a dog’ or ‘mean’ (1,3). Botanical synonyms: Rosa corymbifera Borkh., R. dumetorum Thuill., and R. ciliatosepala Blocki (2,6). FAMILY: Rosaceae, the rose family (1) Quick Notable Features: ¬ Alternate, odd-pinnately compound, serrate leaves ¬ Conspicuous stipules, fused to petiole ¬ Showy white/pink flowers with many stamens and pistils in a hypanthium ¬ Bright red hips with no sepals Plant Height: R. canina grows up to 3m tall (10). Subspecies/varieties recognized (6,7): Rosa canina var. dumetorum (Thuill.) Poir., Rosa canina var. canina L., Rosa canina var. corymbifera Rouy, Rosa canina var. andegavensis Arechav., Rosa canina var. evanida (Christ) P.V.Heath, Rosa canina var. frutetorum (Besser) P.V.Heath, Rosa canina var. libertiae (Dumort.) P.V.Heath, Rosa canina var. Montana (Vill.) P.V.Heath, Rosa canina var. sepium Arechav., Rosa canina var. subcanina (Christ) P.V.Heath, Rosa canina subsp. andegavensis (Bastard) Vigo, Rosa canina subsp. virens (Wahlenb.) Šmite. Most Likely Confused with: Rosa eglanteria, R. micrantha, R. setigera, R multiflora, and Rubus ssp. (1,9). Habitat Preference: The species is found in open, disturbed habitats such as roadsides, old pastures, fields, dry banks, and thickets. R. canina requires at least partial sun, and high levels of soil moisture (1,5,9,10). Geographic Distribution in Michigan: The species grows in six counties of the lower peninsula: Benzie, Hillsdale, Kent, Leelanau, Lenawee, and Wayne (2,19). Known Elevational Distribution: In Turkey, R. -
Vegetation Classification and Mapping Project Report
U.S. Geological Survey-National Park Service Vegetation Mapping Program Acadia National Park, Maine Project Report Revised Edition – October 2003 Mention of trade names or commercial products does not constitute endorsement or recommendation for use by the U. S. Department of the Interior, U. S. Geological Survey. USGS-NPS Vegetation Mapping Program Acadia National Park U.S. Geological Survey-National Park Service Vegetation Mapping Program Acadia National Park, Maine Sara Lubinski and Kevin Hop U.S. Geological Survey Upper Midwest Environmental Sciences Center and Susan Gawler Maine Natural Areas Program This report produced by U.S. Department of the Interior U.S. Geological Survey Upper Midwest Environmental Sciences Center 2630 Fanta Reed Road La Crosse, Wisconsin 54603 and Maine Natural Areas Program Department of Conservation 159 Hospital Street 93 State House Station Augusta, Maine 04333-0093 In conjunction with Mike Story (NPS Vegetation Mapping Coordinator) NPS, Natural Resources Information Division, Inventory and Monitoring Program Karl Brown (USGS Vegetation Mapping Coordinator) USGS, Center for Biological Informatics and Revised Edition - October 2003 USGS-NPS Vegetation Mapping Program Acadia National Park Contacts U.S. Department of Interior United States Geological Survey - Biological Resources Division Website: http://www.usgs.gov U.S. Geological Survey Center for Biological Informatics P.O. Box 25046 Building 810, Room 8000, MS-302 Denver Federal Center Denver, Colorado 80225-0046 Website: http://biology.usgs.gov/cbi Karl Brown USGS Program Coordinator - USGS-NPS Vegetation Mapping Program Phone: (303) 202-4240 E-mail: [email protected] Susan Stitt USGS Remote Sensing and Geospatial Technologies Specialist USGS-NPS Vegetation Mapping Program Phone: (303) 202-4234 E-mail: [email protected] Kevin Hop Principal Investigator U.S. -
Rubus Rosifolius Smith: a New Record of an Alien Species in the Flora of Ecuador
BioInvasions Records (2020) Volume 9, Issue 4: 712–722 CORRECTED PROOF Rapid Communication Rubus rosifolius Smith: a new record of an alien species in the flora of Ecuador David A. Espinel-Ortiz and Katya Romoleroux* Laboratorio de Botánica Sistemática, Escuela de Ciencias Biológicas, Facultad de Ciencias Exactas y Naturales, Pontificia Universidad Católica del Ecuador, Av. 12 de Octubre 1076 y Roca, Quito, Ecuador Author e-mails: [email protected] (DAEO), [email protected], [email protected] (KR) *Corresponding author Citation: Espinel-Ortiz DA, Romoleroux K (2020) Rubus rosifolius Smith: a new Abstract record of an alien species in the flora of Ecuador. BioInvasions Records 9(4): 712– A new record of Rubus (Rosaceae) for Ecuador is described: R. rosifolius, a climbing 722, https://doi.org/10.3391/bir.2020.9.4.05 shrub introduced and naturalized in the Ecuadorian Andes for its edible fruits. We provide an updated key for the genus Rubus in Ecuador, a detailed description of Received: 18 March 2020 the species, and its distribution. In addition, photographs of this species and complete Accepted: 15 June 2020 illustrations are included. Published: 25 August 2020 Handling editor: Anibal Pauchard Key words: cultivated, Ecuadorian Andes, introduced, Idaeobatus, raspberry, Thematic editor: Stelios Katsanevakis Rosaceae Copyright: © Espinel-Ortiz DA and Romoleroux K This is an open access article distributed under terms of the Creative Commons Attribution License Introduction (Attribution 4.0 International - CC BY 4.0). Rubus L., included in the subfamily Rosoideae and tribe Rubeae, is one of OPEN ACCESS. the most numerous genera of the Rosaceae family with approximately 400– 700 species (Judd et al. -
Terrestrial and Palustrine Plant Communities of Pennsylvania
ACKNOWLEDGEMENTS unding for this project was provided by the Wild Resource Conservation Fund. Data used in the development of this classification came largely from Pennsylvania Natural Diversity Inventory F partners: The Nature Conservancy, DCNR's Bureau of Forestry, and the Western Pennsylvania Conservancy. Tom Smith's 1991 draft "Natural Ecological Communities of Pennsylvania" provided the foundation upon which this classification was built. This effort owes much to its predecessor. This work relies heavily on the expertise and many years of field experience provided by the following people: Tony Davis, Dan Devlin, Charles Bier, Andra Leimanis, Jeff Wagner, Mark Anderson, Roger Earl Latham. Several of these people provided draft community descriptions, species lists, or environmental descriptions of community types. All of these people have reviewed multiple draft versions of this classification and have given generously of their time, wisdom, and experience. Many thanks to all of the people who reviewed earlier drafts of this classification, and provided suggestions, guidance, technical assistance, and encouragement, including: Ashton Berdine John Kunsman Jim Bissell Julie Lundgren Dave Boyd Kathy McKenna Chad Buhrman Ken Metzler Bureau of Forestry Staff Susan Munch Don Cameron Chris Nowak Dick Croop Greg Podniesinski Roger Dorsey Connie Reightler Greg Edinger Carol Reschke Jenni Farber Ann Rhoads Chris Firestone Rich Ring Ted Grisez Ann Robinson Steve Grund Lesley Sneddon Stevens Heckscher Kim Steiner Robert Hill Susan Stout Steve -
Moosehorn Ozone Injury Survey
Evaluation of Ozone Injury On Vegetation in the Moosehorn National Wildlife Refuge Maine 2004 Observations Submitted to The U.S. Fish and Wildlife Service Air Quality Branch Denver, CO Donald D. Davis, Ph.D. April 15, 2005 2 TABLE OF CONTENTS Page TABLE OF CONTENTS 2 INTRODUCTION 3 General 3 Objectives 3 Justification 3 Diagnosis of Air Pollution Injury 7 Description of Refuge 10 METHODS 14 General Survey Areas 14 Preliminary Selection of Bioindicator Species 14 Air Quality 15 Survey Dates and Locations 16 Severity Rating 19 RESULTS AND DISCUSSION 20 Final Selection of Bioindicator Species 20 Foliar Symptoms 21 SUMMARY 32 RELATED LITERATURE 33 APPENDIX (Vegetation List) 35 3 INTRODUCTION General Moosehorn is one of more than 500 Refuges in the National Wildlife Refuge System (NWRS) administered by the U.S. Fish and Wildlife Service (FWS). The NWRS is a network of lands and waters managed specifically for the protection of wildlife and their habitat, and represents the most comprehensive wildlife management program in the world. Units of the system stretch across the United States from northern Alaska to the Florida Keys and include small islands in the Caribbean and South Pacific. The character of the Refuges is as diverse as the nation itself. Moosehorn National Wildlife Refuge (MNWR) was established in 1937 as a refuge and breeding ground for migratory birds and other wildlife. It is the first in a chain of migratory bird refuges that extends from Maine to Florida. The Refuge consists of two units. The Baring Unit covers 16,080 acres and is located off U.S. -
Key to Genera and Families
KEY TO GENERA AND FAMILIES Identification notes: The key is highly artificial and unabashedly pragmatic. One can get to the sub-keys (Key A, Key B, Key A7, etc.) by proceeding through the general key, or by jumping directly to the sub-key based on its “description”. In order to accommodate both access methods, some taxa are keyed in 2 or more sub-keys, but would logically be found only in one sub-key if one proceeded accurately through the general key. For instance, floating aquatic pteridophytes are keyed in both Key A2 and Key C1, though a logical procession through the general Key would key them into Key C1, and not allow them to appear as well in Key A2; they are keyed as well in Key A2, so that if it is apparent or determinable to the user that they are vascular cryptogams, they can be found via that key as well. The arrangement of leaves (alternate, whorled, or opposite) and their disposition (basal or cauline) is used frequently in the keys. Alternate leaves are attached at the stem 1 per node, opposite leaves 2 per node, and whorled leaves 3 or more per node. Note however, that alternate leaves are sometimes (especially at the base of plants or at the tips of woody branches, such as short shoots) arrayed with very short internodes, leading to them being closely clustered and mistakable as whorled or opposite. Note that some plants (Hypericum, Eupatorium, many Lamiaceae, many others) have a strong tendency to have axillary shoots in the axils of primary leaves; these are often referred to as axillary fascicles. -
Preliminary List of Species Native Within the Adirondack Park Listed Alphabetically by Common Name and Sorted by Habit V.1 Updated 10.23.2006
Preliminary List of Species Native Within the Adirondack Park Listed Alphabetically by Common Name and Sorted by Habit v.1 Updated 10.23.2006 Purpose The purpose of this list is to provide an information resource to those wishing to plant or otherwise propagate plants native to the Adirondack Park. It could be used by an individual or a group developing a landscaping plan and wishing to use species native to the Park and a particular county. They could use the list as a source of native species and request nurserymen to provide plant materials from it. Although most of these species are not now available from commercial nurseries, it may be that if continued requests are made for them, the nursery industry would see fit to propagate the desired plants. Requesting and planting natives would reduce the call for non-native and potentially invasive species. It should be noted that some of these species will most likely never be sold commercially because of rarity or difficulty in propagation. The list is meant to being a living document with species added and deleted as additional information is collected and verified. Although it may be tempting, plants should never be harvested from the wild. In fact some of these plants are legally protected, and no harvesting can occur on State lands. Refer to the New York Natural Heritage Program website (http://www.dec.state.ny.us/website/dfwmr/heritage/plants.htm) for a complete treatment of New York State protected plants and federal and State laws regarding rare plants. Source The source of this list is the New York Flora Atlas produced by the New York Flora Association and available online at http://atlas.nyflora.org . -
Renfrew County Plants
Renfrew County Plant Checklist. November 14, 2010. Scientific Name Common Name Author Kingdom Phylum Class Order Family Genus Species Subspecies Abies balsamea Balsam Fir (L.) P. Mill. Plantae Coniferophyta Pinopsida Pinales Pinaceae Abies balsamea Acalypha virginica Virginia Copperleaf L. Plantae Anthophyta Dicotyledoneae Euphorbiales Euphorbiaceae Acalypha virginica Acer negundo Box Elder L. Plantae Anthophyta Dicotyledoneae Sapindales Aceraceae Acer negundo Acer nigrum Black Maple Michx. f. Plantae Anthophyta Dicotyledoneae Sapindales Aceraceae Acer nigrum Acer pensylvanicum Striped Maple L. Plantae Anthophyta Dicotyledoneae Sapindales Aceraceae Acer pensylvanicum Acer platanoides Norway Maple L. Plantae Anthophyta Dicotyledoneae Sapindales Aceraceae Acer platanoides Acer rubrum Red Maple L. Plantae Anthophyta Dicotyledoneae Sapindales Aceraceae Acer rubrum Acer saccharinum Silver Maple L. Plantae Anthophyta Dicotyledoneae Sapindales Aceraceae Acer saccharinum Acer saccharum var. saccharum Sugar Maple Plantae Anthophyta Dicotyledoneae Sapindales Aceraceae Acer saccharum var. saccharum Acer spicatum Mountain Maple Lam. Plantae Anthophyta Dicotyledoneae Sapindales Aceraceae Acer spicatum Acer x freemanii Hybrid Maple E. Murr. Plantae Anthophyta Dicotyledoneae Sapindales Aceraceae Acer x freemanii Achillea millefolium var. millefolium Common Yarrow Plantae Anthophyta Dicotyledoneae Asterales Asteraceae Achillea millefolium var. millefolium Achillea ptarmica False Sneezewort L. Plantae Anthophyta Dicotyledoneae Asterales Asteraceae Achillea -
Leaf Mottling: Relation to Growth Form and Leaf Phenology and Possible Role As Camouflage Author(S): T
Leaf Mottling: Relation to Growth Form and Leaf Phenology and Possible Role as Camouflage Author(s): T. J. Givnish Source: Functional Ecology, Vol. 4, No. 4 (1990), pp. 463-474 Published by: British Ecological Society Stable URL: http://www.jstor.org/stable/2389314 Accessed: 27-04-2016 13:23 UTC Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at http://about.jstor.org/terms JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. British Ecological Society, Wiley are collaborating with JSTOR to digitize, preserve and extend access to Functional Ecology This content downloaded from 130.223.51.59 on Wed, 27 Apr 2016 13:23:21 UTC All use subject to http://about.jstor.org/terms Functional ESSAY REVIEW Ecology 1990, 4, 463-'474 Leaf mottling: relation to growth form and leaf phenology and possible role as camouflage T. J. GIVNISH tion or masking of chlorophyll over portions of the Department of Botany, University of Wisconsin, upper leaf surface, often in a more or less mottled Madison, Wisconsin, USA pattern. Leaves mottled in various shades of green, or marked by splashes or stripes of white (or sometimes purple, red or pink) are characteristic Abstract. The arguments of Smith (1986) bearing of many species of angiosperms, particularly on the adaptive significance of leaf mottling are among understorey herbs in temperate and tropi- criticized and an alternative hypothesis is pre- cal forests (Neger, 1913; Richards, 1952; Morgan, sented. -
RARE NATIVE PLANTS of RHODE ISLAND – September, 2007 Prepared by Richard W
RARE NATIVE PLANTS OF RHODE ISLAND – September, 2007 Prepared by Richard W. Enser Rhode Island Natural Heritage Program Rhode Island Department of Environmental Management Providence, Rhode Island 02908 The flora of Rhode Island includes roughly 1,700 plant taxa of which approximately 1,300 (77%) are considered to be native. The following list identifies those members of the native flora which are the rarest in Rhode Island and most in need of conservation. All taxa listed herein are currently being tracked by the Rhode Island Natural Heritage Program through comprehensive mapping and computerized databases maintained by the Rhode Island Natural History Survey. Information regarding the location and status of rare elements, including plants, animals and natural communities, is used to establish priorities for land preservation and to provide guidance within the environmental review process. The Rhode Island Natural Heritage Program was established in 1978. During the first year of operation an initial listing of rare plants was derived from two previously published lists: Endangered Plants of Rhode Island, by Dr. Irene Stuckey; and Rare and Endangered Vascular Plant Species in Rhode Island, by Dr. George L. Church and Richard L. Champlin. The latter publication was the Rhode Island contribution to a regional assessment of rare plants prepared by the New England Botanical Club in cooperation with the U.S. Fish and Wildlife Service. More recently, the New England Plant Conservation Program (NEPCoP - established in 1991) conducted an exhaustive reassessment of the region’s flora in preparation of Flora Conservanda: New England - the NEPCoP list of plants in need of conservation. -
1. Rosaceae: Taxonomy, Economic Importance, Genomics
1. Rosaceae: Taxonomy, Economic Importance, Genomics Kim E. Hummer and Jules Janick A rose by any other name would smell as sweet. Shakespeare A rose is a rose is a rose. Gertrude Stein The Rose Family The rose is a rose And was always a rose; But the theory now goes That the apple’s a rose, And the pear is, and so’s The plum, I suppose. The dear only knows What will next prove a rose. You, of course, are a rose, But were always a rose. Robert Frost 1 Nomenclature and Taxonomy 1.1 Origins The magnificent simplicity, or to some, the monotonous consistency, of the actin- iomorphic flowers of the rose family has been recognized for millennia. The origin of the name rose is summarized in the American Heritage Dictionary (2000): The English word rose comes from Latin and Old French. Latin rosa may be an Etruscan form of Greek Rhodia, “Rhodian, originating from Rhodes.” The Attic Greek word for rose K.E. Hummer (B) U. S. Department of Agriculture, Agricultural Research Service, National Clonal Germplasm Repository, 33447 Peoria Road, Corvallis, Oregon, 97333, USA K.M. Folta, S.E. Gardiner (eds.), Genetics and Genomics of Rosaceae, Plant Genetics 1 and Genomics: Crops and Models 6, DOI 10.1007/978-0-387-77491-6 1, C Springer Science+Business Media, LLC 2009 2 K.E. Hummer and J. Janick is rhodon, and in Sappho’s Aeolic dialect of Greek it is wrodon. In Avestan, the language of the Persian prophet Zoroaster, “rose” is varda and in Armenian vard, words both related to the Aeolic form. -
Biodiversity of the Potomac River Valley (Work-In-Progress, Draft of 11 April 2013)
Biodiversity of the Potomac River Valley (work-in-progress, draft of 11 April 2013) Edward M. Barrows Laboratory of Biodiversity and Entomology, Georgetown Univerisity, Washington, D.C. _______________________________ _______________________________ Table of Contents Introduction (Goals, Background, Disclaimers, Organism Names) Table 1. Some Large Divisions of Life on Earth. Table 2. Life A. Domain Archaea B. Domain Bacteria C. Domain Eukarya 1. Kingdom Animalia 2. Kingdom Fungi 3. Kingdom Plantae Nonflowering Plants 4. Kingdom Protista Appendix 1. Abbreviations and Definitions Appendix 2. Glossary (taxa and other terms) Appendix 3. Map key. Literature Cited _________________________________ _________________________________ Goals Increase our nature and scientific literacy in view of Earth Stewardship. Learn about local biodiversity. Learn about local plant communities. Pool our knowledge and update this list as a group. _________________________________ This document I started this document in 2009 for my Forest Ecology class, and hope to update it over the years. This is primarily an annotated list of local biota. I include more detailed information for selected taxon in Table 5. For full information you should consult reference books and scientific papers, some of which I list in the References. Please give me corrections, additions, suggestions, etc. A wonderful introduction to the biota of the U.S. Mid-Atlantic Region is Alden, P., B. Cassie, J. D. W. Kahl, E. A. Oches, H. Zirlin, and W. B. Zomlefer. 2007. National Audubon Society. Field Guide to the Mid-Atlantic States. Alfred A. Knopf, New York, NY. 448 pp. _________________________________ Background How do many biologists now classify life from large through small taxonomic groups (= taxa)? (domain, phylum, class, order, family, genus, species, subspecies (variety and forma in plants) and categories between the larger categories) Table 1.