Plant Species of Concern a Program of the Natural Resource Information System, April 2003 Montana State Library
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Toward a Resolution of Campanulid Phylogeny, with Special Reference to the Placement of Dipsacales
TAXON 57 (1) • February 2008: 53–65 Winkworth & al. • Campanulid phylogeny MOLECULAR PHYLOGENETICS Toward a resolution of Campanulid phylogeny, with special reference to the placement of Dipsacales Richard C. Winkworth1,2, Johannes Lundberg3 & Michael J. Donoghue4 1 Departamento de Botânica, Instituto de Biociências, Universidade de São Paulo, Caixa Postal 11461–CEP 05422-970, São Paulo, SP, Brazil. [email protected] (author for correspondence) 2 Current address: School of Biology, Chemistry, and Environmental Sciences, University of the South Pacific, Private Bag, Laucala Campus, Suva, Fiji 3 Department of Phanerogamic Botany, The Swedish Museum of Natural History, Box 50007, 104 05 Stockholm, Sweden 4 Department of Ecology & Evolutionary Biology and Peabody Museum of Natural History, Yale University, P.O. Box 208106, New Haven, Connecticut 06520-8106, U.S.A. Broad-scale phylogenetic analyses of the angiosperms and of the Asteridae have failed to confidently resolve relationships among the major lineages of the campanulid Asteridae (i.e., the euasterid II of APG II, 2003). To address this problem we assembled presently available sequences for a core set of 50 taxa, representing the diver- sity of the four largest lineages (Apiales, Aquifoliales, Asterales, Dipsacales) as well as the smaller “unplaced” groups (e.g., Bruniaceae, Paracryphiaceae, Columelliaceae). We constructed four data matrices for phylogenetic analysis: a chloroplast coding matrix (atpB, matK, ndhF, rbcL), a chloroplast non-coding matrix (rps16 intron, trnT-F region, trnV-atpE IGS), a combined chloroplast dataset (all seven chloroplast regions), and a combined genome matrix (seven chloroplast regions plus 18S and 26S rDNA). Bayesian analyses of these datasets using mixed substitution models produced often well-resolved and supported trees. -
Plant List Bristow Prairie & High Divide Trail
*Non-native Bristow Prairie & High Divide Trail Plant List as of 7/12/2016 compiled by Tanya Harvey T24S.R3E.S33;T25S.R3E.S4 westerncascades.com FERNS & ALLIES Pseudotsuga menziesii Ribes lacustre Athyriaceae Tsuga heterophylla Ribes sanguineum Athyrium filix-femina Tsuga mertensiana Ribes viscosissimum Cystopteridaceae Taxaceae Rhamnaceae Cystopteris fragilis Taxus brevifolia Ceanothus velutinus Dennstaedtiaceae TREES & SHRUBS: DICOTS Rosaceae Pteridium aquilinum Adoxaceae Amelanchier alnifolia Dryopteridaceae Sambucus nigra ssp. caerulea Holodiscus discolor Polystichum imbricans (Sambucus mexicana, S. cerulea) Prunus emarginata (Polystichum munitum var. imbricans) Sambucus racemosa Rosa gymnocarpa Polystichum lonchitis Berberidaceae Rubus lasiococcus Polystichum munitum Berberis aquifolium (Mahonia aquifolium) Rubus leucodermis Equisetaceae Berberis nervosa Rubus nivalis Equisetum arvense (Mahonia nervosa) Rubus parviflorus Ophioglossaceae Betulaceae Botrychium simplex Rubus ursinus Alnus viridis ssp. sinuata Sceptridium multifidum (Alnus sinuata) Sorbus scopulina (Botrychium multifidum) Caprifoliaceae Spiraea douglasii Polypodiaceae Lonicera ciliosa Salicaceae Polypodium hesperium Lonicera conjugialis Populus tremuloides Pteridaceae Symphoricarpos albus Salix geyeriana Aspidotis densa Symphoricarpos mollis Salix scouleriana Cheilanthes gracillima (Symphoricarpos hesperius) Salix sitchensis Cryptogramma acrostichoides Celastraceae Salix sp. (Cryptogramma crispa) Paxistima myrsinites Sapindaceae Selaginellaceae (Pachystima myrsinites) -
Palustriella Pluristratosa Spec. Nov. (Amblystegiaceae, Bryopsida), a New Aquatic Moss Species with Pluristratose Lamina from Switzerland
Palustriella pluristratosa spec. nov. (Amblystegiaceae, Bryopsida), a new aquatic moss species with pluristratose lamina from Switzerland Autor(en): Stech, Michael / Frahm, Jan-Peter Objekttyp: Article Zeitschrift: Botanica Helvetica Band (Jahr): 111 (2001) Heft 2 PDF erstellt am: 06.10.2021 Persistenter Link: http://doi.org/10.5169/seals-73905 Nutzungsbedingungen Die ETH-Bibliothek ist Anbieterin der digitalisierten Zeitschriften. Sie besitzt keine Urheberrechte an den Inhalten der Zeitschriften. Die Rechte liegen in der Regel bei den Herausgebern. Die auf der Plattform e-periodica veröffentlichten Dokumente stehen für nicht-kommerzielle Zwecke in Lehre und Forschung sowie für die private Nutzung frei zur Verfügung. Einzelne Dateien oder Ausdrucke aus diesem Angebot können zusammen mit diesen Nutzungsbedingungen und den korrekten Herkunftsbezeichnungen weitergegeben werden. Das Veröffentlichen von Bildern in Print- und Online-Publikationen ist nur mit vorheriger Genehmigung der Rechteinhaber erlaubt. Die systematische Speicherung von Teilen des elektronischen Angebots auf anderen Servern bedarf ebenfalls des schriftlichen Einverständnisses der Rechteinhaber. Haftungsausschluss Alle Angaben erfolgen ohne Gewähr für Vollständigkeit oder Richtigkeit. Es wird keine Haftung übernommen für Schäden durch die Verwendung von Informationen aus diesem Online-Angebot oder durch das Fehlen von Informationen. Dies gilt auch für Inhalte Dritter, die über dieses Angebot zugänglich sind. Ein Dienst der ETH-Bibliothek ETH Zürich, Rämistrasse 101, 8092 -
Prospects for Biological Control of Ambrosia Artemisiifolia in Europe: Learning from the Past
DOI: 10.1111/j.1365-3180.2011.00879.x Prospects for biological control of Ambrosia artemisiifolia in Europe: learning from the past EGERBER*,USCHAFFNER*,AGASSMANN*,HLHINZ*,MSEIER & HMU¨ LLER-SCHA¨ RERà *CABI Europe-Switzerland, Dele´mont, Switzerland, CABI Europe-UK, Egham, Surrey, UK, and àDepartment of Biology, Unit of Ecology & Evolution, University of Fribourg, Fribourg, Switzerland Received 18 November 2010 Revised version accepted 16 June 2011 Subject Editor: Paul Hatcher, Reading, UK management approach. Two fungal pathogens have Summary been reported to adversely impact A. artemisiifolia in the The recent invasion by Ambrosia artemisiifolia (common introduced range, but their biology makes them unsuit- ragweed) has, like no other plant, raised the awareness able for mass production and application as a myco- of invasive plants in Europe. The main concerns herbicide. In the native range of A. artemisiifolia, on the regarding this plant are that it produces a large amount other hand, a number of herbivores and pathogens of highly allergenic pollen that causes high rates of associated with this plant have a very narrow host range sensitisation among humans, but also A. artemisiifolia is and reduce pollen and seed production, the stage most increasingly becoming a major weed in agriculture. sensitive for long-term population management of this Recently, chemical and mechanical control methods winter annual. We discuss and propose a prioritisation have been developed and partially implemented in of these biological control candidates for a classical or Europe, but sustainable control strategies to mitigate inundative biological control approach against its spread into areas not yet invaded and to reduce its A. -
Biological Control of Two Ageratina Species (Asteraceae: Eupatorieae) in South Africa
Biological control of two Ageratina species (Asteraceae: Eupatorieae) in South Africa F. Heystek1*, A.R. Wood2, S. Neser1 & Y. Kistensamy1 1Agricultural Research Council-Plant Protection Research Institute, Private Bag X134, Queenswood, 0121 South Africa 2Agricultural Research Council-Plant Protection Research Institute, Private Bag X5017, Stellenbosch, 7599 South Africa Ageratina adenophora (Spreng.) R.M.King & H.Rob. and Ageratina riparia (Regel) R.M.King & H.Rob. (Asteraceae: Eupatorieae), originally from Mexico, are invasive in many countries. These plants produce thousands of wind- and water-dispersed seeds which enable them to spread rapidly and invade stream banks and moist habitats in areas with high rainfall. Two biological control agents, a shoot-galling fly, Procecidochares utilis Stone (Diptera: Tephri- tidae), and a leaf-spot fungus, Passalora ageratinae Crous & A.R. Wood (Mycosphaerellales: Mycosphaerellaceae), were introduced against A. adenophora in South Africa in 1984 and 1987, respectively. Both established but their impact is considered insufficient. Exploratory trips to Mexico between 2007 and 2009 to search for additional agents on A. adenophora produced a gregarious leaf-feeding moth, Lophoceramica sp. (Lepidoptera: Noctuidae), a stem-boring moth, probably Eugnosta medioxima (Razowski) (Lepidoptera: Tortricidae), a leaf-mining beetle, Pentispa fairmairei (Chapuis) (Coleoptera: Chrysomelidae: Cassidinae), and a leaf-rust, Baeodromus eupatorii (Arthur) Arthur (Pucciniales: Pucciniosiraceae) all of which have been subjected to preliminary investigations. Following its success in Hawaii, the white smut fungus, Entyloma ageratinae R.W. Barreto & H.C. Evans (Entylomatales: Entylomataceae), was introduced in 1989 to South Africa against A. riparia. Its impact has not been evaluated since its establishment in 1990 in South Africa. By 2009, however, A. -
U·M·I University Microfilms International a 8Ell & Howell Information Company 300 North Zeeb Road
Patterns of homoplasy in North American Astragalus L. (Fabaceae). Item Type text; Dissertation-Reproduction (electronic) Authors Sanderson, Michael John. Publisher The University of Arizona. Rights Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. Download date 10/10/2021 18:39:52 Link to Item http://hdl.handle.net/10150/184764 INFORMATION TO USERS The most advanced technology has been used to photo graph and reproduce this manuscript from the microfilm master. UMI films the text directly from the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter face, while others may be from any type of computer printer. The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send UIVn a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion. Oversize materials (e.g., maps, drawings, charts) are re produced by sectioning the original, beginning at the upper left-hand corner and continuing from left to right in equal sections with small overlaps. Each original is also photographed in one exposure and is included in reduced form at the back of the book. -
Northern Fen Communitynorthern Abstract Fen, Page 1
Northern Fen CommunityNorthern Abstract Fen, Page 1 Community Range Prevalent or likely prevalent Infrequent or likely infrequent Absent or likely absent Photo by Joshua G. Cohen Overview: Northern fen is a sedge- and rush-dominated 8,000 years. Expansion of peatlands likely occurred wetland occurring on neutral to moderately alkaline following climatic cooling, approximately 5,000 years saturated peat and/or marl influenced by groundwater ago (Heinselman 1970, Boelter and Verry 1977, Riley rich in calcium and magnesium carbonates. The 1989). community occurs north of the climatic tension zone and is found primarily where calcareous bedrock Several other natural peatland communities also underlies a thin mantle of glacial drift on flat areas or occur in Michigan and can be distinguished from shallow depressions of glacial outwash and glacial minerotrophic (nutrient-rich) northern fens, based on lakeplains and also in kettle depressions on pitted comparisons of nutrient levels, flora, canopy closure, outwash and moraines. distribution, landscape context, and groundwater influence (Kost et al. 2007). Northern fen is dominated Global and State Rank: G3G5/S3 by sedges, rushes, and grasses (Mitsch and Gosselink 2000). Additional open wetlands occurring on organic Range: Northern fen is a peatland type of glaciated soils include coastal fen, poor fen, prairie fen, bog, landscapes of the northern Great Lakes region, ranging intermittent wetland, and northern wet meadow. Bogs, from Michigan west to Minnesota and northward peat-covered wetlands raised above the surrounding into central Canada (Ontario, Manitoba, and Quebec) groundwater by an accumulation of peat, receive inputs (Gignac et al. 2000, Faber-Langendoen 2001, Amon of nutrients and water primarily from precipitation et al. -
Monument Rock Wilderness Baker County, OR T14S R36E S20, 21, 27, 28, 29, 33, 34 Compiled by Paul Slichter
Monument Rock Wilderness Baker County, OR T14S R36E S20, 21, 27, 28, 29, 33, 34 Compiled by Paul Slichter. Updated January 9, 2011 Flora Northwest: http://science.halleyhosting.com Common Name Scientific Name Family Gray's Lovage Ligusticum grayi Apiaceae Mountain Sweet Cicely Osmorhiza berteroi Apiaceae Western Sweet Cicely Osmorhiza occidentalis Apiaceae Purple Sweet Cicely Osmorhiza purpurea ? Apiaceae Sierra Snake Root Sanicula graveolens Apiaceae Yarrow Achillea millefolium Asteraceae Western Boneset Ageratina occidentalis Asteraceae Orange Agoseris Agoseris aurantiaca Asteraceae Mountain Agoseris Agoseris monticola? Asteraceae Rosy Pussytoes Antennaria rosea Asteraceae Heart-leaf Arnica Arnica cordifolia Asteraceae Hairy Arnica Arnica mollis Asteraceae Big Sagebrush Artemisia tridentata ssp. vaseyana Asteraceae Leafy Aster ? Symphyotrichum foliaceum ? Asteraceae Green Horsebrush Chrysothamnus viscidiflorus Asteraceae Long-leaved Hawksbeard Crepis acuminata Asteraceae Gray Hawksbeard Crepis intermedia Asteraceae Green Rabbitbrush Chrysothamnus viscidiflorus (ssp. ?) Asteraceae Bloomer's Daisy Erigeron bloomeri v. bloomeri Asteraceae Cutleaf Daisy Erigeron compositus v. discoidea Asteraceae Eaton's Shaggy Fleabane Erigeron eatonii v. villosus Asteraceae Subalpine Daisy Erigeron glacialis Asteraceae Woolly Sunflower Eriophyllum lanatum v. integrifolium Asteraceae Rabbitbrush Goldenweed Ericameria bloomeri? Asteraceae Greene's Goldenweed Ericameria greenii Asteraceae White-flowered Hawkweed Hieracium albiflorum? Asteraceae Scouler's -
2.10 Meesia Longiseta HEDW. Code: 1389 Anhang: II
2.10 Meesia longiseta HEDW. Code: 1389 Anhang: II KLAUS WEDDELING, GERHARD LUDWIG & MONIKA HACHTEL, Bonn Namen: D: Langstieliges Schwanenhalsmoos, Langstieliges Meesemoos, Gestreckte Langborste E: Long-stalked Thread Moss, Long-shafted Swan Moss, F: – Systematik/Taxonomie: Bryophyta, Bryopsida, Bryidae, Splachnales, Meesiaceae. Synonyme: Amblyodon longisetus (HEDW.) P. BEAUV. Kennzeichen/Artbestimmung: Meesia longiseta ist ein 4–8 (–10) cm hohes, akrokarpes, unverzweigtes Laubmoos von grün-schwärzlicher Färbung. Die Art wächst in lockeren, weichen Rasen (Abb. 2.9). Das Stämmchen ist bis in die Spitze wurzelhaarig und im Moose Querschnitt dreikantig. Die Blättchen sind mehr oder weniger deutlich in 3 oder 6 Rei- hen angeordnet und vom Stämmchen abgespreizt. Die 2–3,5 mm langen, spitzen Blätt- chen laufen deutlich am Stämmchen herab, sind oberwärts gekielt, ganzrandig oder an der Spitze etwas gezähnt. Ihre deutlich entwickelte Rippe endet unterhalb der Blattspitze. Der Blattrand ist flach. Die Laminazellen sind rechteckig bis rhombisch und etwa 14 µm breit. Die rötlichen, gedrehten Seten der synözischen Art können über 10 cm lang wer- den. Die langbirnenförmige, aufrechte Kapsel hat einen deutlichen Hals. Bei der Spo- renreife im Juni und Juli werden die mit 36–44 µm Durchmesser recht großen Sporen frei- gesetzt. Die Chromosomenzahl ist nicht bekannt (FRITSCH 1991). Differenzierende Merkmale zu den ähnlichen Arten Meesia uliginosa und M. hexasticha sind der nicht ein- gerollte Blattrand, die kleineren Sporen und der Rippenquerschnitt mit kleinen, inneren Zellen (zusammengestellt nach CRUM & ANDERSON 1981, FRAHM 1979, LIMPRICHT 1895). Abbildungen der Art finden sich bei CRUM & ANDERSON (1981, Fig. 296, 297, S. 628, 629: Blättchen, Blattspitze, Habitus, Kapsel) und FRAHM (1979, Fig. -
Conservation Strategy for Allotropa Virgata (Candystick), U.S
CONSERVATION STRATEGY FOR ALLOTROPA VIRGATA (CANDYSTICK), U.S. FOREST SERVICE, NORTHERN AND INTERMOUNTAIN REGIONS by Juanita Lichthardt Conservation Data Center Natural Resource Policy Bureau October, 1995 Idaho Department of Fish and Game 600 South Walnut, P.O. Box 25 Boise, Idaho 83707 Jerry M. Conley, Director Cooperative Challenge Cost-share Project Nez Perce National Forest Idaho Department of Fish and Game Purchase Order No.:95-17-20-001 ACKNOWLEDGMENTS I am grateful to the following Forest Service sensitive plant coordinators and botanists who went out of their way to provide valuable consultation, maps, and data: Leonard Lake, Linda Pietarinen, Jim Anderson, Quinn Carver, Alexia Cochrane, and John Joy. These same people are largely responsible for our current level of knowledge about Allotropa virgata. Special thanks to Janet Johnson and Marilyn Olson who found the time to show me Allotropa sites on the Bitterroot and Payette National Forests, respectively. Steve Shelly, Montana Natural Heritage Program/US Forest Service, initiated this project and provided thoughtful review. I hope that this document provides both the practical guidance and theoretical basis needed for a coordinated effort by management agencies toward conservation of Allotropa virgata. i ABSTRACT This conservation strategy provides recommendations for management of National Forest lands supporting and adjoining populations of Allotropa virgata (candystick), a plant species designated as sensitive in Regions 1 and 4 of the US Forest Service. Allotropa virgata presents a special conservation challenge because it is part of a three-way symbiosis involving conifers and their ectomycorrhizal fungi. First, the current state of our knowledge of the species is summarized, including distribution, habitat, ecology, population biology, monitoring results, past impacts, and perceived threats. -
Phylogeny and Phylogenetic Taxonomy of Dipsacales, with Special Reference to Sinadoxa and Tetradoxa (Adoxaceae)
PHYLOGENY AND PHYLOGENETIC TAXONOMY OF DIPSACALES, WITH SPECIAL REFERENCE TO SINADOXA AND TETRADOXA (ADOXACEAE) MICHAEL J. DONOGHUE,1 TORSTEN ERIKSSON,2 PATRICK A. REEVES,3 AND RICHARD G. OLMSTEAD 3 Abstract. To further clarify phylogenetic relationships within Dipsacales,we analyzed new and previously pub- lished rbcL sequences, alone and in combination with morphological data. We also examined relationships within Adoxaceae using rbcL and nuclear ribosomal internal transcribed spacer (ITS) sequences. We conclude from these analyses that Dipsacales comprise two major lineages:Adoxaceae and Caprifoliaceae (sensu Judd et al.,1994), which both contain elements of traditional Caprifoliaceae.Within Adoxaceae, the following relation- ships are strongly supported: (Viburnum (Sambucus (Sinadoxa (Tetradoxa, Adoxa)))). Combined analyses of C ap ri foliaceae yield the fo l l ow i n g : ( C ap ri folieae (Diervilleae (Linnaeeae (Morinaceae (Dipsacaceae (Triplostegia,Valerianaceae)))))). On the basis of these results we provide phylogenetic definitions for the names of several major clades. Within Adoxaceae, Adoxina refers to the clade including Sinadoxa, Tetradoxa, and Adoxa.This lineage is marked by herbaceous habit, reduction in the number of perianth parts,nectaries of mul- ticellular hairs on the perianth,and bifid stamens. The clade including Morinaceae,Valerianaceae, Triplostegia, and Dipsacaceae is here named Valerina. Probable synapomorphies include herbaceousness,presence of an epi- calyx (lost or modified in Valerianaceae), reduced endosperm,and distinctive chemistry, including production of monoterpenoids. The clade containing Valerina plus Linnaeeae we name Linnina. This lineage is distinguished by reduction to four (or fewer) stamens, by abortion of two of the three carpels,and possibly by supernumerary inflorescences bracts. Keywords: Adoxaceae, Caprifoliaceae, Dipsacales, ITS, morphological characters, phylogeny, phylogenetic taxonomy, phylogenetic nomenclature, rbcL, Sinadoxa, Tetradoxa. -
Mosses of Qinghai-Tibetan Plateau, China
J. Hattori Bot. Lab. No. 82: 305- 320 (July 1997) MOSSES OF QINGHAI-TIBETAN PLATEAU, CHINA 1 2 BENITO C. TAN AND JIA Yu ABSTRACT . A total of 57 genera and 109 species of mosses are reported based on collections made from the 1995 expedition to Yushu Prefecture of Qinghai province. Didymodon gaochienii and Or thomitrium schofieldii are described new to science. Encalypta intermedia, Hygrohypnum po/are and Leptopterygynandrum austro-alpinum are three moss records that have not previously been reported from China. Significant range extensions . are reported for Amblyodon dealbatum, Conardia compacta, Distichium hagenii, Grimmia anodon, Leptopterygynandrum subintegrum, Oedipodium gri.ffithianum, Orthotrichum pumilum, Philonotis calcarea, Plagiobryum demissum and Pylaisiella falcata . In addition, four new synonyms are proposed with their respective accepted names placed in side brackets: Aloina rubripila Aziz & Vohra [ =Aloina rigida var. obliquifolia (C. Muell.) Delgad.], Barbu/a anserino-capitata X.-J. Li [=Didymodonjohansenii (Williams) Zand.], Barbu/a longicosta ta X-J. Li [=Didymodon constrictus var. jlexicaulis (Chen) Saito] and Tortu/a longimucronata X.-J. Li [=Syntrichia ruralis (Hedw.) Web. & Mohr]. INTRODUCTION The province of Qinghai, with an area of about 720,000 sq. km, is the fourth largest province in China. It consitutes the eastern flank of the massive Tibetan plateau. The nu merous mountain glaciers in the province form the headwater of many great river systems in China and Indochina, such as Yellow River, Yangtze River and Mekong River. Because of its great distance from the ocean, the prevailing climate is strongly continental with in tense diurnal changes of daily temperature and a long winter season.