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"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. -
Cally Plant List a ACIPHYLLA Horrida
Cally Plant List A ACIPHYLLA horrida ACONITUM albo-violaceum albiflorum ABELIOPHYLLUM distichum ACONITUM cultivar ABUTILON vitifolium ‘Album’ ACONITUM pubiceps ‘Blue Form’ ACAENA magellanica ACONITUM pubiceps ‘White Form’ ACAENA species ACONITUM ‘Spark’s Variety’ ACAENA microphylla ‘Kupferteppich’ ACONITUM cammarum ‘Bicolor’ ACANTHUS mollis Latifolius ACONITUM cammarum ‘Franz Marc’ ACANTHUS spinosus Spinosissimus ACONITUM lycoctonum vulparia ACANTHUS ‘Summer Beauty’ ACONITUM variegatum ACANTHUS dioscoridis perringii ACONITUM alboviolaceum ACANTHUS dioscoridis ACONITUM lycoctonum neapolitanum ACANTHUS spinosus ACONITUM paniculatum ACANTHUS hungaricus ACONITUM species ex. China (Ron 291) ACANTHUS mollis ‘Long Spike’ ACONITUM japonicum ACANTHUS mollis free-flowering ACONITUM species Ex. Japan ACANTHUS mollis ‘Turkish Form’ ACONITUM episcopale ACANTHUS mollis ‘Hollard’s Gold’ ACONITUM ex. Russia ACANTHUS syriacus ACONITUM carmichaelii ‘Spätlese’ ACER japonicum ‘Aconitifolium’ ACONITUM yezoense ACER palmatum ‘Filigree’ ACONITUM carmichaelii ‘Barker’s Variety’ ACHILLEA grandifolia ACONITUM ‘Newry Blue’ ACHILLEA ptarmica ‘Perry’s White’ ACONITUM napellus ‘Bergfürst’ ACHILLEA clypeolata ACONITUM unciniatum ACIPHYLLA monroi ACONITUM napellus ‘Blue Valley’ ACIPHYLLA squarrosa ACONITUM lycoctonum ‘Russian Yellow’ ACIPHYLLA subflabellata ACONITUM japonicum subcuneatum ACONITUM meta-japonicum ADENOPHORA aurita ACONITUM napellus ‘Carneum’ ADIANTUM aleuticum ‘Japonicum’ ACONITUM arcuatum B&SWJ 774 ADIANTUM aleuticum ‘Miss Sharples’ ACORUS calamus ‘Argenteostriatus’ -
Pima County Plant List (2020) Common Name Exotic? Source
Pima County Plant List (2020) Common Name Exotic? Source McLaughlin, S. (1992); Van Abies concolor var. concolor White fir Devender, T. R. (2005) McLaughlin, S. (1992); Van Abies lasiocarpa var. arizonica Corkbark fir Devender, T. R. (2005) Abronia villosa Hariy sand verbena McLaughlin, S. (1992) McLaughlin, S. (1992); Van Abutilon abutiloides Shrubby Indian mallow Devender, T. R. (2005) Abutilon berlandieri Berlandier Indian mallow McLaughlin, S. (1992) Abutilon incanum Indian mallow McLaughlin, S. (1992) McLaughlin, S. (1992); Van Abutilon malacum Yellow Indian mallow Devender, T. R. (2005) Abutilon mollicomum Sonoran Indian mallow McLaughlin, S. (1992) Abutilon palmeri Palmer Indian mallow McLaughlin, S. (1992) Abutilon parishii Pima Indian mallow McLaughlin, S. (1992) McLaughlin, S. (1992); UA Abutilon parvulum Dwarf Indian mallow Herbarium; ASU Vascular Plant Herbarium Abutilon pringlei McLaughlin, S. (1992) McLaughlin, S. (1992); UA Abutilon reventum Yellow flower Indian mallow Herbarium; ASU Vascular Plant Herbarium McLaughlin, S. (1992); Van Acacia angustissima Whiteball acacia Devender, T. R. (2005); DBGH McLaughlin, S. (1992); Van Acacia constricta Whitethorn acacia Devender, T. R. (2005) McLaughlin, S. (1992); Van Acacia greggii Catclaw acacia Devender, T. R. (2005) Acacia millefolia Santa Rita acacia McLaughlin, S. (1992) McLaughlin, S. (1992); Van Acacia neovernicosa Chihuahuan whitethorn acacia Devender, T. R. (2005) McLaughlin, S. (1992); UA Acalypha lindheimeri Shrubby copperleaf Herbarium Acalypha neomexicana New Mexico copperleaf McLaughlin, S. (1992); DBGH Acalypha ostryaefolia McLaughlin, S. (1992) Acalypha pringlei McLaughlin, S. (1992) Acamptopappus McLaughlin, S. (1992); UA Rayless goldenhead sphaerocephalus Herbarium Acer glabrum Douglas maple McLaughlin, S. (1992); DBGH Acer grandidentatum Sugar maple McLaughlin, S. (1992); DBGH Acer negundo Ashleaf maple McLaughlin, S. -
New York Non-Native Plant Invasiveness Ranking Form
NEW YORK NON -NATIVE PLANT INVASIVENESS RANKING FORM Scientific name: Callitriche stagnalis Scop. USDA Plants Code: CAST Common names: pond water-starwort Native distribution: Europe, Asia, North Africa Date assessed: July 1, 2008 Assessors: Steve Clemants Reviewers: LIISMA SRC Date Approved: July 9, 2008 Form version date: 10 July 2009 New York Invasiveness Rank: Low (Relative Maximum Score 40.00-49.99) Distribution and Invasiveness Rank (Obtain from PRISM invasiveness ranking form ) PRISM Status of this species in each PRISM: Current Distribution Invasiveness Rank 1 Adirondack Park Invasive Program Not Assessed Not Assessed 2 Capital/Mohawk Not Assessed Not Assessed 3 Catskill Regional Invasive Species Partnership Not Assessed Not Assessed 4 Finger Lakes Not Assessed Not Assessed 5 Long Island Invasive Species Management Area Restricted Insignificant 6 Lower Hudson Not Assessed Not Assessed 7 Saint Lawrence/Eastern Lake Ontario Not Assessed Not Assessed 8 Western New York Not Assessed Not Assessed Invasiveness Ranking Summary Total (Total Answered*) Total (see details under appropriate sub-section) Possible 1 Ecological impact 40 (30) 9 2 Biological characteristic and dispersal ability 25 (22 ) 12 3 Ecological amplitude and distribution 25 (25) 15 4 Difficulty of control 10 (3) 3 Outcome score 100 (80 )b 39a † Relative maximum score 48.75 § New York Invasiveness Rank Low (Relative Maximum Score 40.00-49.99) * For questions answered “unknown” do not include point value in “Total Answered Points Possible.” If “Total Answered Points Possible” is less than 70.00 points, then the overall invasive rank should be listed as “Unknown.” †Calculated as 100(a/b) to two decimal places. -
Well-Known Plants in Each Angiosperm Order
Well-known plants in each angiosperm order This list is generally from least evolved (most ancient) to most evolved (most modern). (I’m not sure if this applies for Eudicots; I’m listing them in the same order as APG II.) The first few plants are mostly primitive pond and aquarium plants. Next is Illicium (anise tree) from Austrobaileyales, then the magnoliids (Canellales thru Piperales), then monocots (Acorales through Zingiberales), and finally eudicots (Buxales through Dipsacales). The plants before the eudicots in this list are considered basal angiosperms. This list focuses only on angiosperms and does not look at earlier plants such as mosses, ferns, and conifers. Basal angiosperms – mostly aquatic plants Unplaced in order, placed in Amborellaceae family • Amborella trichopoda – one of the most ancient flowering plants Unplaced in order, placed in Nymphaeaceae family • Water lily • Cabomba (fanwort) • Brasenia (watershield) Ceratophyllales • Hornwort Austrobaileyales • Illicium (anise tree, star anise) Basal angiosperms - magnoliids Canellales • Drimys (winter's bark) • Tasmanian pepper Laurales • Bay laurel • Cinnamon • Avocado • Sassafras • Camphor tree • Calycanthus (sweetshrub, spicebush) • Lindera (spicebush, Benjamin bush) Magnoliales • Custard-apple • Pawpaw • guanábana (soursop) • Sugar-apple or sweetsop • Cherimoya • Magnolia • Tuliptree • Michelia • Nutmeg • Clove Piperales • Black pepper • Kava • Lizard’s tail • Aristolochia (birthwort, pipevine, Dutchman's pipe) • Asarum (wild ginger) Basal angiosperms - monocots Acorales -
Healing Process Induced by a Flavonic Fraction of Bidens Aurea on Chronic Gastric Lesion in Rat
Healing Process Induced by a Flavonic Fraction of Bidens aurea on Chronic Gastric Lesion in Rat. Role of Angiogenesis and Neutrophil Inhibition M. J. Martín Calero, C. La Casa, V. Motilva, A. López and C. Alarcón de la Lastra Laboratorio de Farmacologfa, Facultad de Farmacia, Universidad de Sevilla, 41012 Sevilla, Espana Z. Naturforsch. 51c, 570-577 (1996); received March 11/May 21, 1996 Bidens aurea, Flavonoids. Chronic Gastric Ulcer, Neutrophils, Myeloperoxidase Activity The aim of this study was to elucidate the mechanism of the healing process mediated by the flavonic fraction of Bidens aurea on chronic gastric ulceration induced by 5% acetic acid in rats. The diethyl ether extract (125 and 62.5 mg kg -1 body weight) was administered in a single doses, 7 and 14 days after provocation of lesions. Our results demonstrated that both doses significantly decreased the macro and microscopic ulcer index. Usually after 14-days treatment the lesions were found completely covered with regenerative epithelium and also an important proliferation of blood vessels was observed. Myeloperoxidase (M PO ) activity was assayed and used as an index of leucocyte infiltration. Application of acetic acid pro duced a significant increase of this activity 7 days after induction of chronic injury. A dm in istration of 125 mg kg 1 of the ether extract provoked a sharp reduction on the enzymatic activity at the same period. After 14 days, this decrease was higher with both doses (p<0.001). In addition, the macroscopic examination showed a drastic reduction of leucocyte infiltration in treated groups. These results suggest that the recovery of vascularization of the ulcerated area and the decrease of neutrophil infiltration are involved in the antiulcerogenic effect of the flavonoid fraction of Bidens aurea. -
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 -
ASTERACEAE José Ángel Villarreal-Quintanilla* José Luis Villaseñor-Ríos** Rosalinda Medina-Lemos**
FLORA DEL VALLE DE TEHUACÁN-CUICATLÁN Fascículo 62. ASTERACEAE José Ángel Villarreal-Quintanilla* José Luis Villaseñor-Ríos** Rosalinda Medina-Lemos** *Departamento de Botánica Universidad Autónoma Agraria Antonio Narro **Departamento de Botánica Instituto de Biología, UNAM INSTITUTO DE BIOLOGÍA UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO 2008 Primera edición: octubre de 2008 D.R. © Universidad Nacional Autónoma de México Instituto de Biología. Departamento de Botánica ISBN 968-36-3108-8 Flora del Valle de Tehuacán-Cuicatlán ISBN 970-32-5084-4 Fascículo 62 Dirección de los autores: Departamento de Botánica Universidad Autónoma Agraria Antonio Narro Buenavista, Saltillo C.P. 25315 Coahuila, México Universidad Nacional Autónoma de México Instituto de Biología. Departamento de Botánica. 3er. Circuito de Ciudad Universitaria Coyoacán, 04510. México, D.F. 1 En la portada: 2 1. Mitrocereus fulviceps (cardón) 2. Beaucarnea purpusii (soyate) 3 4 3. Agave peacockii (maguey fibroso) 4. Agave stricta (gallinita) Dibujo de Elvia Esparza FLORA DEL VALLE DE TEHUACÁN-CUICATLÁN 62: 1-59. 2008 ASTERACEAE1 Bercht. & J.Presl Tribu Tageteae José Ángel Villarreal-Quintanilla José Luis Villaseñor-Ríos Rosalinda Medina-Lemos Bibliografía. Bremer, K. 1994. Asteraceae. Cladistics & Classification. Timber Press. Portland, Oregon. 752 p. McVaugh, R. 1984. Compositae. In: W.R. Anderson (ed.). Flora Novo-Galiciana. Ann Arbor The University of Michi- gan Press 12: 40-42. Panero, J.L. & V.A. Funk. 2002. Toward a phylogene- tic subfamily classification for the Compositae (Asteraceae). Proc. Biol. Soc. Washington 115: 909-922. Villaseñor Ríos, J.L. 1993. La familia Asteraceae en México. Rev. Soc. Mex. Hist. Nat. 44: 117-124. Villaseñor Ríos, J.L. 2003. Diversidad y distribución de las Magnoliophyta de México. -
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. -
Introduction to Common Native & Invasive Freshwater Plants in Alaska
Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska Cover photographs by (top to bottom, left to right): Tara Chestnut/Hannah E. Anderson, Jamie Fenneman, Vanessa Morgan, Dana Visalli, Jamie Fenneman, Lynda K. Moore and Denny Lassuy. Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska This document is based on An Aquatic Plant Identification Manual for Washington’s Freshwater Plants, which was modified with permission from the Washington State Department of Ecology, by the Center for Lakes and Reservoirs at Portland State University for Alaska Department of Fish and Game US Fish & Wildlife Service - Coastal Program US Fish & Wildlife Service - Aquatic Invasive Species Program December 2009 TABLE OF CONTENTS TABLE OF CONTENTS Acknowledgments ............................................................................ x Introduction Overview ............................................................................. xvi How to Use This Manual .................................................... xvi Categories of Special Interest Imperiled, Rare and Uncommon Aquatic Species ..................... xx Indigenous Peoples Use of Aquatic Plants .............................. xxi Invasive Aquatic Plants Impacts ................................................................................. xxi Vectors ................................................................................. xxii Prevention Tips .................................................... xxii Early Detection and Reporting -
December 2012 Number 1
Calochortiana December 2012 Number 1 December 2012 Number 1 CONTENTS Proceedings of the Fifth South- western Rare and Endangered Plant Conference Calochortiana, a new publication of the Utah Native Plant Society . 3 The Fifth Southwestern Rare and En- dangered Plant Conference, Salt Lake City, Utah, March 2009 . 3 Abstracts of presentations and posters not submitted for the proceedings . 4 Southwestern cienegas: Rare habitats for endangered wetland plants. Robert Sivinski . 17 A new look at ranking plant rarity for conservation purposes, with an em- phasis on the flora of the American Southwest. John R. Spence . 25 The contribution of Cedar Breaks Na- tional Monument to the conservation of vascular plant diversity in Utah. Walter Fertig and Douglas N. Rey- nolds . 35 Studying the seed bank dynamics of rare plants. Susan Meyer . 46 East meets west: Rare desert Alliums in Arizona. John L. Anderson . 56 Calochortus nuttallii (Sego lily), Spatial patterns of endemic plant spe- state flower of Utah. By Kaye cies of the Colorado Plateau. Crystal Thorne. Krause . 63 Continued on page 2 Copyright 2012 Utah Native Plant Society. All Rights Reserved. Utah Native Plant Society Utah Native Plant Society, PO Box 520041, Salt Lake Copyright 2012 Utah Native Plant Society. All Rights City, Utah, 84152-0041. www.unps.org Reserved. Calochortiana is a publication of the Utah Native Plant Society, a 501(c)(3) not-for-profit organi- Editor: Walter Fertig ([email protected]), zation dedicated to conserving and promoting steward- Editorial Committee: Walter Fertig, Mindy Wheeler, ship of our native plants. Leila Shultz, and Susan Meyer CONTENTS, continued Biogeography of rare plants of the Ash Meadows National Wildlife Refuge, Nevada. -
Chromosome Numbers in Compositae, XII: Heliantheae
SMITHSONIAN CONTRIBUTIONS TO BOTANY 0 NCTMBER 52 Chromosome Numbers in Compositae, XII: Heliantheae Harold Robinson, A. Michael Powell, Robert M. King, andJames F. Weedin SMITHSONIAN INSTITUTION PRESS City of Washington 1981 ABSTRACT Robinson, Harold, A. Michael Powell, Robert M. King, and James F. Weedin. Chromosome Numbers in Compositae, XII: Heliantheae. Smithsonian Contri- butions to Botany, number 52, 28 pages, 3 tables, 1981.-Chromosome reports are provided for 145 populations, including first reports for 33 species and three genera, Garcilassa, Riencourtia, and Helianthopsis. Chromosome numbers are arranged according to Robinson’s recently broadened concept of the Heliantheae, with citations for 212 of the ca. 265 genera and 32 of the 35 subtribes. Diverse elements, including the Ambrosieae, typical Heliantheae, most Helenieae, the Tegeteae, and genera such as Arnica from the Senecioneae, are seen to share a specialized cytological history involving polyploid ancestry. The authors disagree with one another regarding the point at which such polyploidy occurred and on whether subtribes lacking higher numbers, such as the Galinsoginae, share the polyploid ancestry. Numerous examples of aneuploid decrease, secondary polyploidy, and some secondary aneuploid decreases are cited. The Marshalliinae are considered remote from other subtribes and close to the Inuleae. Evidence from related tribes favors an ultimate base of X = 10 for the Heliantheae and at least the subfamily As teroideae. OFFICIALPUBLICATION DATE is handstamped in a limited number of initial copies and is recorded in the Institution’s annual report, Smithsonian Year. SERIESCOVER DESIGN: Leaf clearing from the katsura tree Cercidiphyllumjaponicum Siebold and Zuccarini. Library of Congress Cataloging in Publication Data Main entry under title: Chromosome numbers in Compositae, XII.