Utah Flora: Apiaceae (Umbelliferae)
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The Plant Press the ARIZONA NATIVE PLANT SOCIETY
The Plant Press THE ARIZONA NATIVE PLANT SOCIETY Volume 36, Number 1 Summer 2013 In this Issue: Plants of the Madrean Archipelago 1-4 Floras in the Madrean Archipelago Conference 5-8 Abstracts of Botanical Papers Presented in the Madrean Archipelago Conference Southwest Coralbean (Erythrina flabelliformis). Plus 11-19 Conservation Priority Floras in the Madrean Archipelago Setting for Arizona G1 Conference and G2 Plant Species: A Regional Assessment by Thomas R. Van Devender1. Photos courtesy the author. & Our Regular Features Today the term ‘bioblitz’ is popular, meaning an intensive effort in a short period to document the diversity of animals and plants in an area. The first bioblitz in the southwestern 2 President’s Note United States was the 1848-1855 survey of the new boundary between the United States and Mexico after the Treaty of Guadalupe Hidalgo of 1848 ended the Mexican-American War. 8 Who’s Who at AZNPS The border between El Paso, Texas and the Colorado River in Arizona was surveyed in 1855- 9 & 17 Book Reviews 1856, following the Gadsden Purchase in 1853. Besides surveying and marking the border with monuments, these were expeditions that made extensive animal and plant collections, 10 Spotlight on a Native often by U.S. Army physicians. Botanists John M. Bigelow (Charphochaete bigelovii), Charles Plant C. Parry (Agave parryi), Arthur C. V. Schott (Stephanomeria schotti), Edmund K. Smith (Rhamnus smithii), George Thurber (Stenocereus thurberi), and Charles Wright (Cheilanthes wrightii) made the first systematic plant collection in the Arizona-Sonora borderlands. ©2013 Arizona Native Plant In 1892-94, Edgar A. Mearns collected 30,000 animal and plant specimens on the second Society. -
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 -
Sensitive Plant Species
SENSITIVE PLANT SPECIES Barneby Woody Aster (Aster kingii var. barnebyana) Barneby’s woody aster is a member of the sunflower family (Asteraceae) and it grows from a well-developed taproot. There are persistent blackish or dark brown, old leaf bases at the base of the plant. The stems are short (3-12 cm long) and the herbage is covered with glandular hairs. The leaves are basal, 0.8-12 cm long, and oblanceolate to spatulate in shape with 1-10 pronounced teeth. Flowers occur in clusters of 1-5, standing 8-11 mm high. The inner bracts are often purplish and at least the outer tips are bent backward. The ray flowers are white, often fading to pale pink. This plant flowers between August and September. This species is found in mountain mahogany and oak communities on rock outcrops composed of Precambian quartzite. This endemic species of the Canyon Mountains in Millard and Juab Counties, Utah has been reported in 15 element occurrence records as of 2002 (Madsen 2002). These scattered occurrences indicate a total population of 600+ plants. The range of elevation is between 7,500 and 9640. Major associated species are Holodiscus dumosus (Mountain spray), Huechera rubescens (Red alumroot), Symphoricarpos oreophilus (Mountain snowberry), Quercus gambelii (Gambel’s oak), and Eriogonum brevicaule (Shortstem buckwheat) (Franklin 1990). To date there are 15 known occurrences of this species on the Fillmore Ranger District of the Fishlake National Forest (Franklin 1990). Plants are harbored from threats such as livestock grazing by their occurrence on steep rock outcrops. 40 Bicknell milkvetch (Astragalus consobrinus) The Bicknell milkvetch is a member of the pea family (Fabaceae). -
Major Lineages Within Apiaceae Subfamily Apioideae: a Comparison of Chloroplast Restriction Site and Dna Sequence Data1
American Journal of Botany 86(7): 1014±1026. 1999. MAJOR LINEAGES WITHIN APIACEAE SUBFAMILY APIOIDEAE: A COMPARISON OF CHLOROPLAST RESTRICTION SITE AND DNA SEQUENCE DATA1 GREGORY M. PLUNKETT2 AND STEPHEN R. DOWNIE Department of Plant Biology, University of Illinois, Urbana, Illinois 61801 Traditional sources of taxonomic characters in the large and taxonomically complex subfamily Apioideae (Apiaceae) have been confounding and no classi®cation system of the subfamily has been widely accepted. A restriction site analysis of the chloroplast genome from 78 representatives of Apioideae and related groups provided a data matrix of 990 variable characters (750 of which were potentially parsimony-informative). A comparison of these data to that of three recent DNA sequencing studies of Apioideae (based on ITS, rpoCl intron, and matK sequences) shows that the restriction site analysis provides 2.6± 3.6 times more variable characters for a comparable group of taxa. Moreover, levels of divergence appear to be well suited to studies at the subfamilial and tribal levels of Apiaceae. Cladistic and phenetic analyses of the restriction site data yielded trees that are visually congruent to those derived from the other recent molecular studies. On the basis of these comparisons, six lineages and one paraphyletic grade are provisionally recognized as informal groups. These groups can serve as the starting point for future, more intensive studies of the subfamily. Key words: Apiaceae; Apioideae; chloroplast genome; restriction site analysis; Umbelliferae. Apioideae are the largest and best-known subfamily of tem, and biochemical characters exhibit similarly con- Apiaceae (5 Umbelliferae) and include many familiar ed- founding parallelisms (e.g., Bell, 1971; Harborne, 1971; ible plants (e.g., carrot, parsnips, parsley, celery, fennel, Nielsen, 1971). -
Aegopodium Podagraria
Aegopodium podagraria INTRODUCTORY DISTRIBUTION AND OCCURRENCE BOTANICAL AND ECOLOGICAL CHARACTERISTICS FIRE EFFECTS AND MANAGEMENT MANAGEMENT CONSIDERATIONS APPENDIX: FIRE REGIME TABLE REFERENCES INTRODUCTORY AUTHORSHIP AND CITATION FEIS ABBREVIATION NRCS PLANT CODE COMMON NAMES TAXONOMY SYNONYMS LIFE FORM Variegated goutweed. All-green goutweed. Photos by John Randall, The Nature Conservancy, Bugwood.org AUTHORSHIP AND CITATION: Waggy, Melissa, A. 2010. Aegopodium podagraria. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/ [ 2010, January 21]. FEIS ABBREVIATION: AEGPOD NRCS PLANT CODE [87]: AEPO COMMON NAMES: goutweed bishop's goutweed bishop's weed bishopsweed ground elder herb Gerard TAXONOMY: The scientific name of goutweed is Aegopodium podagraria L. (Apiaceae) [40]. SYNONYMS: Aegopodium podagraria var. podagraria [71] Aegopodium podagraria var. variegatum Bailey [40,71] LIFE FORM: Forb DISTRIBUTION AND OCCURRENCE SPECIES: Aegopodium podagraria GENERAL DISTRIBUTION HABITAT TYPES AND PLANT COMMUNITIES GENERAL DISTRIBUTION: Goutweed was introduced in North America from Europe [82]. In the United States, goutweed occurs from Maine south to South Carolina and west to Minnesota and Missouri. It also occurs in the Pacific Northwest from Montana to Washington and Oregon. It occurs in all the Canadian provinces excepting Newfoundland and Labrador, and Alberta. Plants Database provides a distributional map of goutweed. Globally, goutweed occurs primarily in the northern hemisphere, particularly in Europe, Asia Minor ([28,36,58,92], reviews by [14,27]), and Russia (review by [27,63]). Goutweed's native distribution is unclear. It may have been introduced in England (review by [2]) and is considered a "weed" in the former Soviet Union, Germany, Finland (Holm 1979 cited in [14]), and Poland [44]. -
Washington Plant List Douglas County by Scientific Name
The NatureMapping Program Washington Plant List Revised: 9/15/2011 Douglas County by Scientific Name (1) Non- native, (2) ID Scientific Name Common Name Plant Family Invasive √ 763 Acer glabrum Douglas maple Aceraceae 800 Alisma graminium Narrowleaf waterplantain Alismataceae 19 Alisma plantago-aquatica American waterplantain Alismataceae 1087 Rhus glabra Sumac Anacardiaceae 650 Rhus radicans Poison ivy Anacardiaceae 29 Angelica arguta Sharp-tooth angelica Apiaceae 809 Angelica canbyi Canby's angelica Apiaceae 915 Cymopteris terebinthinus Turpentine spring-parsley Apiaceae 167 Heracleum lanatum Cow parsnip Apiaceae 991 Ligusticum grayi Gray's lovage Apiaceae 709 Lomatium ambiguum Swale desert-parsley Apiaceae 997 Lomatium canbyi Canby's desert-parsley Apiaceae 573 Lomatium dissectum Fern-leaf biscuit-root Apiaceae 582 Lomatium geyeri Geyer's desert-parsley Apiaceae 586 Lomatium gormanii Gorman's desert-parsley Apiaceae 998 Lomatium grayi Gray's desert-parsley Apiaceae 999 Lomatium hambleniae Hamblen's desert-parsley Apiaceae 609 Lomatium macrocarpum Large-fruited lomatium Apiaceae 1000 Lomatium nudicaule Pestle parsnip Apiaceae 634 Lomatium triternatum Nine-leaf lomatium Apiaceae 474 Osmorhiza chilensis Sweet-cicely Apiaceae 264 Osmorhiza occidentalis Western sweet-cicely Apiaceae 1044 Osmorhiza purpurea Purple sweet-cicely Apiaceae 492 Sanicula graveolens Northern Sierra) sanicle Apiaceae 699 Apocynum androsaemifolium Spreading dogbane Apocynaceae 813 Apocynum cannabinum Hemp dogbane Apocynaceae 681 Asclepias speciosa Showy milkweed Asclepiadaceae -
Okanogan County Plant List by Scientific Name
The NatureMapping Program Washington Plant List Revised: 9/15/2011 Okanogan County by Scientific Name (1) Non- native, (2) ID Scientific Name Common Name Plant Family Invasive √ 763 Acer glabrum Douglas maple Aceraceae 3 Acer macrophyllum Big-leaf maple Aceraceae 800 Alisma graminium Narrowleaf waterplantain Alismataceae 19 Alisma plantago-aquatica American waterplantain Alismataceae 1155 Amaranthus blitoides Prostrate pigweed Amaranthaceae 1087 Rhus glabra Sumac Anacardiaceae 650 Rhus radicans Poison ivy Anacardiaceae 1230 Berula erecta Cutleaf water-parsnip Apiaceae 774 Cicuta douglasii Water-hemlock Apiaceae 915 Cymopteris terebinthinus Turpentine spring-parsley Apiaceae 167 Heracleum lanatum Cow parsnip Apiaceae 1471 Ligusticum canbyi Canby's lovage Apiaceae 991 Ligusticum grayi Gray's lovage Apiaceae 709 Lomatium ambiguum Swale desert-parsley Apiaceae 1475 Lomatium brandegei Brandegee's lomatium Apiaceae 573 Lomatium dissectum Fern-leaf biscuit-root Apiaceae Coeur d'Alene desert- Lomatium farinosum Apiaceae 548 parsley 582 Lomatium geyeri Geyer's desert-parsley Apiaceae 586 Lomatium gormanii Gorman's desert-parsley Apiaceae 998 Lomatium grayi Gray's desert-parsley Apiaceae 999 Lomatium hambleniae Hamblen's desert-parsley Apiaceae 609 Lomatium macrocarpum Large-fruited lomatium Apiaceae 1476 Lomatium martindalei Few-flowered lomatium Apiaceae 1000 Lomatium nudicaule Pestle parsnip Apiaceae 1477 Lomatium piperi Piper's bisciut-root Apiaceae 634 Lomatium triternatum Nine-leaf lomatium Apiaceae 1528 Osmorhiza berteroi Berter's sweet-cicely -
Bristlecone Chapter of the California Native Plant Society
Dedicated to the Preservation of California Native Flora The California Native Plant Society Bristlecone Chapter Newsletter Volume 40, No. 3 May–June 2019 President’s Message, May 2019 May General Meeting and Potluck Wednesday, May 22nd, 6:00 p.m. potluck, I went for a walk in the Tungsten Hills today and I 7:00–8:00 p.m. presentations was thinking about how I like to hike. The first time I U.S. Forest Service Supervisor’s Office, hiked this trail, I had to go explore every little side 351 Pacu Lane, Bishop road that branched off the trail I had discovered to every piece of mining artifact that I came across. Now Three recipients of the CNPS Bristlecone Chapter I have hiked this nice little loop a few times and I DeDecker Grants will present the findings of their don’t need to go to every hole in the ground or rusty botanical explorations and research of eastern piece of metal, I am satisfied that I already know California. Please join us for a potluck beginning at where those explorations will lead. The joy of this 6pm and presentations at 7pm with desserts. Bring a trail now is seeing how the plants change with the dish to share if you can. seasons. Today, the slopes were predominantly Speakers: yellow with scale bud, desert dandelion, and fiddleneck; the white layia and purple chia accented Sophia Winitsky, the slopes. It was interesting to see that at lower Rancho Santa Ana Botanic Garden elevations the dandelions were the dominate flower, A Flora of Adobe Valley, Mono County but as I moved up the slope, they were replaced by Trevor Carter, UN Reno scale bud. -
The Classification System of the Family Apiaceae in the Flora of Mongolia
Proceedings of the Mongolian Academy of Sciences Vol. 54 No 04 (212) 2014 DOI: http://dx.doi.org/10.5564/pmas.v54i4.624 THE CLASSIFICATION SYSTEM OF THE FAMILY APIACEAE IN THE FLORA OF MONGOLIA Urgamal M. Institute of Botany, Mongolian Academy of Sciences, Ulaanbaatar, Mongolia E-mail: [email protected] Abstract At present time is family Apiaceae consists of 74 species and 37 genera, 5 sub- tribes belong to 12 tribes (4 clades) and 2 sub-families (Saniculoideae and Apioideae) disjunctly distributed in the Mongolian flora. We updated classification system of the family Apiaceae in the flora of Mongolia. Keywords: Classification system, Apiaceae, flora, Mongolia INTRODUCTION The V.I. Grubov (1955) firstly registered species of 30 genera. 46 species, 26 genera in the family Apiaceae. The family Apiaceae family is one of the Then, Ts. Jamsran et al (1972) reported to biggest families in the flora of Mongolia. 14 species of 9 genera and D. Magsar & U. Doing detailed systematical study of the Ligaa (1977) to 6 species of 4 genera, in family, we aimed to reveal species composition addition to previous and D. Magsar & U. of the family in the flora of Mongolia, do Ligaa (1977) concluded the information and morphological, ecological geographical facts of classification, distribution, ecology analysis and molecul biological method of the and habitat on 53 species of 31 genera and V.I. each species, to compare some features used Grubov (1982) on 55 species of 28 genera; for identifying the taxa and revealing higher N. Ulziykhutag (1984) on 65 species of 36 level relationships in the family, and to revise genera; D. -
Apiaceae Lindley (= Umbelliferae A.L.De Jussieu) (Carrot Family)
Apiaceae Lindley (= Umbelliferae A.L.de Jussieu) (Carrot Family) Herbs to lianas, shrubs, or trees, aromatic; stems often hol- Genera/species: 460/4250. Major genera: Schefflera (600 low in internodal region; with secretory canals containing ethe- spp.), Eryngium (230), Polyscias (200), Ferula (150), real oils and resins, triterpenoid saponins, coumarins, falcri- Peucedanum (150), Pimpinella (150), Bupleurum (100), Ore- none polyacetylenes, monoterpenes, and sesquiterpenes; with opanax (90), Hydrocotyle (80), Lomatium (60), Heracleum umbelliferose(a trisaccharide) as carbohydrate storage (60), Angelica (50), Sanicula (40), Chaerophyllum (40), and product. Hairs various, sometimes with prickles. Leaves Aralia (30). Some of the numerous genera occurring in alternate, pinnately or palmately compound to simple, then the continental United States and/or Canada are Angeli- often deeply dissected or lobed, entire to serrate, with pinnate ca, Apium, Aralia, Carum, Centella, Chaerophyllum, Cicuta, to palmate venation; petioles ± sheathing; stipules pres- Conioselinum, Daucus, Eryngium, Hedera, Heradeum, ent to absent. Inflorescences determinate, modified and Hydrocotyle, Ligusticum, Lomatium, Osmorhiza, Oxypolis, forming simple umbels, these arranged in umbels, Panax, Pastinaca, Ptilimnium, Sanicula, Sium, Spermolepis, racemes, spikes, or panicles, sometimes condensed into Thaspium, Torilis, and Zizia. a head, often subtended by an involucre of bracts, termi- nal. Flowers usually bisexual but sometimes unisexual Economic plants and products: Apiaceae contain many (plants then monoecious to dioecious), usually radial, food and spice plants: Anethum (dill), Apium (celery), small. Sepals usually 5, distinct, very reduced. Petals usual- Carum (caraway), Coriandrum (coriander), Cyuminum ly 5, occasionally more, distinct, but developing from a ring (cumin), Daucus (carrot), Foeniculum (fennel), Pastinaca primordium, sometimes clearly connate, often inflexed, (parsnip), Petroselinum (parsley), and Pimpinella (anise). -
Larval Hostplants of Butterflies in Nevada
HOLARCTIC LEPIDOPTERA Editor: Andrei Sourakov Assoc. Editor: Thomas C. Emmel ASSOCIATION FOR TROPICAL VOLUME 12 NUMBER 1-2 August 2008 LEPIDOPTERA Founded 1989 ADVISORY COUNCIL LARVAL HOSTPLANTS James K. Adams (USA) Martin Krüger (South Africa) Andrés O. Angulo (Chile) Tosio Kumata (Japan) OF BUTTERFLIES IN NEVADA Yutaka Arita (Japan) Jean-Francois Landry (Canada) George T. Austin (USA) Torben B. Larsen (England) Jorge Llorente B. (Mexico) Vitor O. Becker, Planaltina, Brazil by Zsolt Bálint (Hungary) Martin Lödl (Austria) Henry S. Barlow (Malaysia) Wolfram Mey (Germany) George T. Austin Dubi Benyamini (Israel) Kauri Mikkola (Finland) Ronald Boender (USA) Scott E. Miller (USA) and Keith S. Brown Jr. (Brazil) Joël Minet (France) José A. Clavijo A. (Venezuela) Eugene G. Munroe (Canada) Patrick J. Leary Charles V. Covell Jr. (USA) K.-T. Park (South Korea) U. Dall’Asta (Belgium) Rod E. Parrott (Canada) Philip J. DeVries (USA) Amnuay Pinratana (Thailand) Julian P. Donahue (USA) Rimantas Puplesis (Lithuania) CONTENTS Eric Garraway (Jamaica) Jozef Razowski (Poland) Dale H. Habeck (USA) M. Alma Solis (USA) INTRODUCTION 1 NYMPHALIDAE 95 Christoph Häuser (Germany) Dieter Stüning (Germany) METHODS 1 Libytheinae 95 Lowell N. Harris (USA) Gerhard Tarmann (Austria) Toshiya Hirowatari (Japan) Paul Thiaucourt (France) LARVAL HOSTPLANTS 2 Heliconiinae 96 Hiroshi Inoue (Japan) Jürgen H. R. Thiele (Germany) HESPERIIDAE 2 Nymphalinae 99 Daniel H. Janzen (USA) Antonio Vives M. (Spain) Kurt Johnson (USA) Hsiau-Yue Wang (Taiwan) Eudaminae 2 Limenitidinae 119 Roger L. Kitching (Australia) Per O. Wickman (Sweden) Pyrginae 2 George O. Krizek (USA) Allen M. Young (USA) Apaturinae 124 Hesperiinae 8 Satyrinae 124 PAPILIONIDAE 14 OFFICERS Danainae 126 President: Ulf Eitschberger, Germany Parnassiinae 14 DISCUSSION 127 Vice-President: Thomas C. -
Plant Species of the Upper Gunnison Basin
Appendix B. Management of Plant Species Contents Federal Interagency Committee for Wetland Delineation I Trees........................................................................................... 788 (1989). II Shrubs ........................................................................................ 791 III Graminoids (Grasses and Grasslike Plants).............................. 806 Descriptive Terminology Code IV Forbs........................................................................................... 819 “Never found in wetlands” not listed or UPL V Ferns and Fern-allies.................................................................. 831 “Generally an upland, nonwetland species” FACU VI Weeds, Introduced Plants, and Poison Plants........................... 831 “Equally likely to be found in wetlands FAC 1. Invasive Plants and Poison Plants.................................... 832 and nonwetlands” 2. Introduced Plants............................................................... 838 “Usually found in wetlands” FACW Table of species and their sites.................................................. 838 “Always found in wetlands” OBL Index to plant species................................................................. 852 2. When production is given below, the units are pounds Notes per acre per year (lb/ac/yr), air-dry weight. Unless otherwise 1. The following words have been used to describe stated, production is given for the above-ground portion of wetland classes found in Reed (1988). “Wetland” as used in live