Black Spruce – Tamarack Palustrine Woodland
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On Tropical Drosera Rotundifolia L
Technical Refereed Contribution On tropical Drosera rotundifolia L. Andreas Fleischmann • Botanische Staatssammlung München and GeoBio-Center LMU University • Menzinger Strasse 67 • D-80638 Munich • Germany • [email protected] Abstract: Two aspects on the morphology and biology of the Philippine population of D. rotundifo- lia were not answered by Coritico and Fleischmann (2016), namely its seed morphology and sea- sonal growth cycle - especially regarding hibernaculum formation, as it is known from its temperate congeners. These gaps can now be covered from observations made from cultivated plants and shall be reported here. Further aspects on the biology of Philippine D. rotundifolia (and other tropical populations of temperate Drosera) in cultivation and natural habitat are presented. Distribution and altitudinal range of Drosera rotundifolia The generic type species of Drosera, Drosera rotundifolia L., is probably the most well-known sundew species, at least to people from the Northern Hemisphere. It is also the most widespread1, its range spans the entire boreal region (Fig. 1; Meusel et al. 1965). Its southernmost populations in the Northern Hemisphere are situated in SE China, in the mountain ranges of northern Guangdong province, at ca. 24.5°N (Coritico & Fleischmann 2016). In Europe its more or less continuous range reaches to ca. 39°N to the south in central Spain, in North America to ca. 34°N in northern Georgia and Alabama states, in Japan to 30°N on the island of Yakushima (Coritico & Fleischmann 2016). Additionally, D. rotundifolia shows a few isolated outlier populations in some areas of the Mediter- ranean [e.g. on the isle of Corsica, France (Delange & Hugot 2020), in the Sierra Nevada of southern Spain (Lorite 2016), and in northern Greece (just three sites known in the Rhodope Mountains; The- odoropoulos & Eleftheriadou 2012)], in central Lebanon (Diels 1906; Tohmé & Tohmé 2007; despite erroneous claims, e.g. -
"National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary."
Intro 1996 National List of Vascular Plant Species That Occur in Wetlands The Fish and Wildlife Service has prepared a National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary (1996 National List). The 1996 National List is a draft revision of the National List of Plant Species That Occur in Wetlands: 1988 National Summary (Reed 1988) (1988 National List). The 1996 National List is provided to encourage additional public review and comments on the draft regional wetland indicator assignments. The 1996 National List reflects a significant amount of new information that has become available since 1988 on the wetland affinity of vascular plants. This new information has resulted from the extensive use of the 1988 National List in the field by individuals involved in wetland and other resource inventories, wetland identification and delineation, and wetland research. Interim Regional Interagency Review Panel (Regional Panel) changes in indicator status as well as additions and deletions to the 1988 National List were documented in Regional supplements. The National List was originally developed as an appendix to the Classification of Wetlands and Deepwater Habitats of the United States (Cowardin et al.1979) to aid in the consistent application of this classification system for wetlands in the field.. The 1996 National List also was developed to aid in determining the presence of hydrophytic vegetation in the Clean Water Act Section 404 wetland regulatory program and in the implementation of the swampbuster provisions of the Food Security Act. While not required by law or regulation, the Fish and Wildlife Service is making the 1996 National List available for review and comment. -
Checklist of Common Native Plants the Diversity of Acadia National Park Is Refl Ected in Its Plant Life; More Than 1,100 Plant Species Are Found Here
National Park Service Acadia U.S. Department of the Interior Acadia National Park Checklist of Common Native Plants The diversity of Acadia National Park is refl ected in its plant life; more than 1,100 plant species are found here. This checklist groups the park’s most common plants into the communities where they are typically found. The plant’s growth form is indicated by “t” for trees and “s” for shrubs. To identify unfamiliar plants, consult a fi eld guide or visit the Wild Gardens of Acadia at Sieur de Monts Spring, where more than 400 plants are labeled and displayed in their habitats. All plants within Acadia National Park are protected. Please help protect the park’s fragile beauty by leaving plants in the condition that you fi nd them. Deciduous Woods ash, white t Fraxinus americana maple, mountain t Acer spicatum aspen, big-toothed t Populus grandidentata maple, red t Acer rubrum aspen, trembling t Populus tremuloides maple, striped t Acer pensylvanicum aster, large-leaved Aster macrophyllus maple, sugar t Acer saccharum beech, American t Fagus grandifolia mayfl ower, Canada Maianthemum canadense birch, paper t Betula papyrifera oak, red t Quercus rubra birch, yellow t Betula alleghaniesis pine, white t Pinus strobus blueberry, low sweet s Vaccinium angustifolium pyrola, round-leaved Pyrola americana bunchberry Cornus canadensis sarsaparilla, wild Aralia nudicaulis bush-honeysuckle s Diervilla lonicera saxifrage, early Saxifraga virginiensis cherry, pin t Prunus pensylvanica shadbush or serviceberry s,t Amelanchier spp. cherry, choke t Prunus virginiana Solomon’s seal, false Maianthemum racemosum elder, red-berried or s Sambucus racemosa ssp. -
Natural Communities of Michigan: Classification and Description
Natural Communities of Michigan: Classification and Description Prepared by: Michael A. Kost, Dennis A. Albert, Joshua G. Cohen, Bradford S. Slaughter, Rebecca K. Schillo, Christopher R. Weber, and Kim A. Chapman Michigan Natural Features Inventory P.O. Box 13036 Lansing, MI 48901-3036 For: Michigan Department of Natural Resources Wildlife Division and Forest, Mineral and Fire Management Division September 30, 2007 Report Number 2007-21 Version 1.2 Last Updated: July 9, 2010 Suggested Citation: Kost, M.A., D.A. Albert, J.G. Cohen, B.S. Slaughter, R.K. Schillo, C.R. Weber, and K.A. Chapman. 2007. Natural Communities of Michigan: Classification and Description. Michigan Natural Features Inventory, Report Number 2007-21, Lansing, MI. 314 pp. Copyright 2007 Michigan State University Board of Trustees. Michigan State University Extension programs and materials are open to all without regard to race, color, national origin, gender, religion, age, disability, political beliefs, sexual orientation, marital status or family status. Cover photos: Top left, Dry Sand Prairie at Indian Lake, Newaygo County (M. Kost); top right, Limestone Bedrock Lakeshore, Summer Island, Delta County (J. Cohen); lower left, Muskeg, Luce County (J. Cohen); and lower right, Mesic Northern Forest as a matrix natural community, Porcupine Mountains Wilderness State Park, Ontonagon County (M. Kost). Acknowledgements We thank the Michigan Department of Natural Resources Wildlife Division and Forest, Mineral, and Fire Management Division for funding this effort to classify and describe the natural communities of Michigan. This work relied heavily on data collected by many present and former Michigan Natural Features Inventory (MNFI) field scientists and collaborators, including members of the Michigan Natural Areas Council. -
Insect Survey of Four Longleaf Pine Preserves
A SURVEY OF THE MOTHS, BUTTERFLIES, AND GRASSHOPPERS OF FOUR NATURE CONSERVANCY PRESERVES IN SOUTHEASTERN NORTH CAROLINA Stephen P. Hall and Dale F. Schweitzer November 15, 1993 ABSTRACT Moths, butterflies, and grasshoppers were surveyed within four longleaf pine preserves owned by the North Carolina Nature Conservancy during the growing season of 1991 and 1992. Over 7,000 specimens (either collected or seen in the field) were identified, representing 512 different species and 28 families. Forty-one of these we consider to be distinctive of the two fire- maintained communities principally under investigation, the longleaf pine savannas and flatwoods. An additional 14 species we consider distinctive of the pocosins that occur in close association with the savannas and flatwoods. Twenty nine species appear to be rare enough to be included on the list of elements monitored by the North Carolina Natural Heritage Program (eight others in this category have been reported from one of these sites, the Green Swamp, but were not observed in this study). Two of the moths collected, Spartiniphaga carterae and Agrotis buchholzi, are currently candidates for federal listing as Threatened or Endangered species. Another species, Hemipachnobia s. subporphyrea, appears to be endemic to North Carolina and should also be considered for federal candidate status. With few exceptions, even the species that seem to be most closely associated with savannas and flatwoods show few direct defenses against fire, the primary force responsible for maintaining these communities. Instead, the majority of these insects probably survive within this region due to their ability to rapidly re-colonize recently burned areas from small, well-dispersed refugia. -
Tamarack (Larix Laricina) by Joyce Tuharsky
Natives to Know: Tamarack (Larix Laricina) By Joyce Tuharsky One of our northernmost trees, the hardy Tamarack is a slender-trunked, conical tree that grows 50-75 feet tall. The needles are a bright blue-green and surprisingly soft. They grow in tight spirals around short knobby spurs along the twigs. Tamaracks are among the few conifers that lose their needles in autumn. Just before the needles drop, the needles turn a beautiful golden-yellow. Tamarack cones are egg-shaped and among the smallest: less than an inch long. The bark is tight and flaky. Under this flaking bark, the wood appears reddish, giving the tree an interesting appearance even without needles. Very cold tolerant, Tamaracks are able to survive temperatures down to −85 °F. They are commonly found at the arctic tree line where it grows as a shrub. In more southerly locations, Tamaracks are normally found in wet soils in swamps, bogs and along lake edges. They are among the first trees to invade filled-lake bogs and are fairly well adapted to reproduce after a fire. However, because of its thin bark and shallow root system, the tree itself does not stand up well to fire. Also, the seedlings do not establish well in shade. Consequently, other more shade tolerant species eventually succeed Tamaracks. Tamaracks are native to much of Canada and south into the northeastern US from Minnesota to West Virginia. Because obits extensive range, the tree is known by many names: American Larch, Eastern Larch, Red Larch, and Hackmatack. The name “Tamarack” is Algonquian and means "wood used for snowshoes."Indeed, because Tamarack wood is very sturdy, yet flexible in thin strips, Native Americans used the wood and roots for many things: snowshoes, toboggans, sewing edges of canoes, and weaving twined bags. -
Natural Landscapes of Maine a Guide to Natural Communities and Ecosystems
Natural Landscapes of Maine A Guide to Natural Communities and Ecosystems by Susan Gawler and Andrew Cutko Natural Landscapes of Maine A Guide to Natural Communities and Ecosystems by Susan Gawler and Andrew Cutko Copyright © 2010 by the Maine Natural Areas Program, Maine Department of Conservation 93 State House Station, Augusta, Maine 04333-0093 All rights reserved. No part of this book may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, or by any information storage and retrieval system without written permission from the authors or the Maine Natural Areas Program, except for inclusion of brief quotations in a review. Illustrations and photographs are used with permission and are copyright by the contributors. Images cannot be reproduced without expressed written consent of the contributor. ISBN 0-615-34739-4 To cite this document: Gawler, S. and A. Cutko. 2010. Natural Landscapes of Maine: A Guide to Natural Communities and Ecosystems. Maine Natural Areas Program, Maine Department of Conservation, Augusta, Maine. Cover photo: Circumneutral Riverside Seep on the St. John River, Maine Printed and bound in Maine using recycled, chlorine-free paper Contents Page Acknowledgements ..................................................................................... 3 Foreword ..................................................................................................... 4 Introduction ............................................................................................... -
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. -
Superior National Forest
Admirals & Relatives Subfamily Limenitidinae Skippers Family Hesperiidae £ Viceroy Limenitis archippus Spread-wing Skippers Subfamily Pyrginae £ Silver-spotted Skipper Epargyreus clarus £ Dreamy Duskywing Erynnis icelus £ Juvenal’s Duskywing Erynnis juvenalis £ Northern Cloudywing Thorybes pylades Butterflies of the £ White Admiral Limenitis arthemis arthemis Superior Satyrs Subfamily Satyrinae National Forest £ Common Wood-nymph Cercyonis pegala £ Common Ringlet Coenonympha tullia £ Northern Pearly-eye Enodia anthedon Skipperlings Subfamily Heteropterinae £ Arctic Skipper Carterocephalus palaemon £ Mancinus Alpine Erebia disa mancinus R9SS £ Red-disked Alpine Erebia discoidalis R9SS £ Little Wood-satyr Megisto cymela Grass-Skippers Subfamily Hesperiinae £ Pepper & Salt Skipper Amblyscirtes hegon £ Macoun’s Arctic Oeneis macounii £ Common Roadside-Skipper Amblyscirtes vialis £ Jutta Arctic Oeneis jutta (R9SS) £ Least Skipper Ancyloxypha numitor Northern Crescent £ Eyed Brown Satyrodes eurydice £ Dun Skipper Euphyes vestris Phyciodes selenis £ Common Branded Skipper Hesperia comma £ Indian Skipper Hesperia sassacus Monarchs Subfamily Danainae £ Hobomok Skipper Poanes hobomok £ Monarch Danaus plexippus £ Long Dash Polites mystic £ Peck’s Skipper Polites peckius £ Tawny-edged Skipper Polites themistocles £ European Skipper Thymelicus lineola LINKS: http://www.naba.org/ The U.S. Department of Agriculture (USDA) prohibits discrimination http://www.butterfliesandmoths.org/ in all its programs and activities on the basis of race, color, national -
2003 Contents
THE NEWSJOURNAL OF THE TORONTO ENTOMOLOGISTS’ ASSOCIATION VOLUME 8, NUMBER 2 JANUARY 2003 Contents Vol. 8, No. 2 Jan. 2003 Mission Statement The Toronto Entomologists’ Association (TEA) is a non-profit educational and scientific organization formed to promote Announcements ...................................................................................................................... 21 interest in insects, to encourage co-operation Upcoming Meetings ............................................................................................................... 22 among amateur and professional Recent News submitted by Don Davis ................................................................................... 24 entomologists, to educate and inform non- entomologists about insects, entomology and Meeting Reports ..................................................................................................................... 25 related fields, to aid in the preservation of Rediscovery of the Lake Huron Locust in Ontario by Steve Marshall .............................. 26 insects and their habitats and to issue publications in support of these objectives. The Bookworm ....................................................................................................................... 27 Executive Officers: Weaving an Ant's Tail by Lydia Attard ................................................................................ 28 President Nancy van der Poorten 2002 Presqu'ile Butterfly Blitz by Philip Careless ............................................................. -
Carnivorous Plant Newsletter Vol 48 No 4 December 2019
Drosera in the western USA—an update Barry A. Rice • Center for Plant Diversity • University of California • One Shields Avenue • Davis • California 95616 • USA • [email protected] Keywords: Taxonomy: Drosera, western USA, Drosera anglica, Drosera intermedia, Drosera linearis, Drosera × obovata, Drosera rotundifolia, Drosera × woodii. One of my primary research activities focuses on carnivorous plants in the US states of Montana, Wyoming, Colorado, New Mexico, and westward (but excluding Alaska). Throughout most of this range, the only native species of Drosera are Drosera rotundifolia L., Drosera anglica Huds., and the hybrid Drosera × obovata Mert. & Koch. These species are well-known to readers of this jour- nal, and need no further description. In this region, these plants quite often occur in sites that are widely separated, and in some states these taxa are of considerable rarity (for example, in Colorado D. rotundifolia and D. anglica are known at only 4 and 1 sites, respectively; Wolf et al. 2006). In addition to these species, there have been reports of two additional native Drosera—Drosera intermedia Hayne in northern Idaho (and perhaps adjacent eastern Washington), and Drosera lin- earis Goldie in Montana. Drosera intermedia was reported in Boundary County, Idaho by Bursik (1993), as growing with Drosera anglica, but being quite different in form. Additional populations were subsequently found in Custer County, Idaho (L. Kinter, pers. comm. 2017). Of course, the closest other Drosera inter- media plants were on the other side of the continent, so this was considered a find of great interest, and the plants were treated as of special significance. A few years ago, I decided I needed to visit and assess these plants. -
Larix Laricina (Du Roi) K
Plant Guide Various wildlife eat the seeds, seedlings, and bark TAMARACK and birds use the trees for nesting. Larix laricina (Du Roi) K. Status Koch Please consult the PLANTS Web site and your State Plant Symbol = LALA Department of Natural Resources for this plant’s current status, such as, state noxious status and Contributed by: USDA NRCS National Plant Data wetland indicator values. Center & the Biota of North America Program Description General: Pine Family (Pinaceae). Native trees growing to 20 meters tall, strongly self-pruning, with a straight, slender trunk and narrow, open, pyramidal crown that occupies one-third to one-half the bole length 25-30 years; branches whorled, horizontal or slightly ascending; short (spur) shoots prominent on twigs 2 years or more old. Bark of young trees is gray, smooth, becoming reddish brown and scaly. Leaves are deciduous, needlelike, 1-2 cm long, pale blue-green, produced in clusters on short shoots or singly along the long shoots, yellowing and shed in the fall. Seed cones are 1-2 cm long, upright; seeds winged, the bodies 2-3 mm long. The common name is the Algonquian Indian name for the plant. Variation within the species: the Alaskan populations of Larix laricina have been described as a different species (Larix alaskensis = Larix laricina var. alaskensis) on the basis of narrower cone scales and bracts, but the variability is now generally recognized as within the range of other populations of the species. Genetic differences in photoperiodic response, germination, and growth patterns have been documented among trees taken from various parts of R.