An Illustrated Key to the Brassicaceae of Alberta
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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) -
Natural Heritage Program List of Rare Plant Species of North Carolina 2016
Natural Heritage Program List of Rare Plant Species of North Carolina 2016 Revised February 24, 2017 Compiled by Laura Gadd Robinson, Botanist John T. Finnegan, Information Systems Manager North Carolina Natural Heritage Program N.C. Department of Natural and Cultural Resources Raleigh, NC 27699-1651 www.ncnhp.org C ur Alleghany rit Ashe Northampton Gates C uc Surry am k Stokes P d Rockingham Caswell Person Vance Warren a e P s n Hertford e qu Chowan r Granville q ot ui a Mountains Watauga Halifax m nk an Wilkes Yadkin s Mitchell Avery Forsyth Orange Guilford Franklin Bertie Alamance Durham Nash Yancey Alexander Madison Caldwell Davie Edgecombe Washington Tyrrell Iredell Martin Dare Burke Davidson Wake McDowell Randolph Chatham Wilson Buncombe Catawba Rowan Beaufort Haywood Pitt Swain Hyde Lee Lincoln Greene Rutherford Johnston Graham Henderson Jackson Cabarrus Montgomery Harnett Cleveland Wayne Polk Gaston Stanly Cherokee Macon Transylvania Lenoir Mecklenburg Moore Clay Pamlico Hoke Union d Cumberland Jones Anson on Sampson hm Duplin ic Craven Piedmont R nd tla Onslow Carteret co S Robeson Bladen Pender Sandhills Columbus New Hanover Tidewater Coastal Plain Brunswick THE COUNTIES AND PHYSIOGRAPHIC PROVINCES OF NORTH CAROLINA Natural Heritage Program List of Rare Plant Species of North Carolina 2016 Compiled by Laura Gadd Robinson, Botanist John T. Finnegan, Information Systems Manager North Carolina Natural Heritage Program N.C. Department of Natural and Cultural Resources Raleigh, NC 27699-1651 www.ncnhp.org This list is dynamic and is revised frequently as new data become available. New species are added to the list, and others are dropped from the list as appropriate. -
The Vascular Plants of Massachusetts
The Vascular Plants of Massachusetts: The Vascular Plants of Massachusetts: A County Checklist • First Revision Melissa Dow Cullina, Bryan Connolly, Bruce Sorrie and Paul Somers Somers Bruce Sorrie and Paul Connolly, Bryan Cullina, Melissa Dow Revision • First A County Checklist Plants of Massachusetts: Vascular The A County Checklist First Revision Melissa Dow Cullina, Bryan Connolly, Bruce Sorrie and Paul Somers Massachusetts Natural Heritage & Endangered Species Program Massachusetts Division of Fisheries and Wildlife Natural Heritage & Endangered Species Program The Natural Heritage & Endangered Species Program (NHESP), part of the Massachusetts Division of Fisheries and Wildlife, is one of the programs forming the Natural Heritage network. NHESP is responsible for the conservation and protection of hundreds of species that are not hunted, fished, trapped, or commercially harvested in the state. The Program's highest priority is protecting the 176 species of vertebrate and invertebrate animals and 259 species of native plants that are officially listed as Endangered, Threatened or of Special Concern in Massachusetts. Endangered species conservation in Massachusetts depends on you! A major source of funding for the protection of rare and endangered species comes from voluntary donations on state income tax forms. Contributions go to the Natural Heritage & Endangered Species Fund, which provides a portion of the operating budget for the Natural Heritage & Endangered Species Program. NHESP protects rare species through biological inventory, -
Chromosomal Evolution and Apomixis in the Cruciferous Tribe Boechereae
fpls-11-00514 May 26, 2020 Time: 17:57 # 1 ORIGINAL RESEARCH published: 28 May 2020 doi: 10.3389/fpls.2020.00514 Chromosomal Evolution and Apomixis in the Cruciferous Tribe Boechereae Terezie Mandáková1, Petra Hloušková1, Michael D. Windham2, Thomas Mitchell-Olds2, Kaylynn Ashby3, Bo Price3, John Carman3 and Martin A. Lysak1* 1 CEITEC, Masaryk University, Brno, Czechia, 2 Department of Biology, Duke University, Durham, NC, United States, 3 Plants, Soils, and Climate Department, Utah State University, Logan, UT, United States The mustard family (Brassicaceae) comprises several dozen monophyletic clades usually ranked as tribes. The tribe Boechereae plays a prominent role in plant research due to the incidence of apomixis and its close relationship to Arabidopsis. This tribe, largely confined to western North America, harbors nine genera and c. 130 species, with >90% of species belonging to the genus Boechera. Hundreds of apomictic diploid and triploid Boechera hybrids have spurred interest in this genus, but the remaining Boechereae genomes remain virtually unstudied. Here we report on comparative Edited by: genome structure of six genera (Borodinia, Cusickiella, Phoenicaulis, Polyctenium, Steven Dodsworth, Nevada, and Sandbergia) and three Boechera species as revealed by comparative University of Bedfordshire, United Kingdom chromosome painting (CCP). All analyzed taxa shared the same seven-chromosome Reviewed by: genome structure. Comparisons with the sister Halimolobeae tribe (n = 8) showed Ana Paula Moraes, that the ancestral Boechereae genome (n = 7) was derived from an older n = 8 Universidade Federal do ABC, Brazil Aretuza Sousa Dos Santos, genome by descending dysploidy followed by the divergence of extant Boechereae Ludwig Maximilian University taxa. -
Plant Species of Special Concern and Vascular Plant Flora of the National
Plant Species of Special Concern and Vascular Plant Flora of the National Elk Refuge Prepared for the US Fish and Wildlife Service National Elk Refuge By Walter Fertig Wyoming Natural Diversity Database The Nature Conservancy 1604 Grand Avenue Laramie, WY 82070 February 28, 1998 Acknowledgements I would like to thank the following individuals for their assistance with this project: Jim Ozenberger, ecologist with the Jackson Ranger District of Bridger-Teton National Forest, for guiding me in his canoe on Flat Creek and for providing aerial photographs and lodging; Jennifer Whipple, Yellowstone National Park botanist, for field assistance and help with field identification of rare Carex species; Dr. David Cooper of Colorado State University, for sharing field information from his 1994 studies; Dr. Ron Hartman and Ernie Nelson of the Rocky Mountain Herbarium, for providing access to unmounted collections by Michele Potkin and others from the National Elk Refuge; Dr. Anton Reznicek of the University of Michigan, for confirming the identification of several problematic Carex specimens; Dr. Robert Dorn for confirming the identification of several vegetative Salix specimens; and lastly Bruce Smith and the staff of the National Elk Refuge for providing funding and logistical support and for allowing me free rein to roam the refuge for plants. 2 Table of Contents Page Introduction . 6 Study Area . 6 Methods . 8 Results . 10 Vascular Plant Flora of the National Elk Refuge . 10 Plant Species of Special Concern . 10 Species Summaries . 23 Aster borealis . 24 Astragalus terminalis . 26 Carex buxbaumii . 28 Carex parryana var. parryana . 30 Carex sartwellii . 32 Carex scirpoidea var. scirpiformis . -
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 -
Taxa Named in Honor of Ihsan A. Al-Shehbaz
TAXA NAMED IN HONOR OF IHSAN A. AL-SHEHBAZ 1. Tribe Shehbazieae D. A. German, Turczaninowia 17(4): 22. 2014. 2. Shehbazia D. A. German, Turczaninowia 17(4): 20. 2014. 3. Shehbazia tibetica (Maxim.) D. A. German, Turczaninowia 17(4): 20. 2014. 4. Astragalus shehbazii Zarre & Podlech, Feddes Repert. 116: 70. 2005. 5. Bornmuellerantha alshehbaziana Dönmez & Mutlu, Novon 20: 265. 2010. 6. Centaurea shahbazii Ranjbar & Negaresh, Edinb. J. Bot. 71: 1. 2014. 7. Draba alshehbazii Klimeš & D. A. German, Bot. J. Linn. Soc. 158: 750. 2008. 8. Ferula shehbaziana S. A. Ahmad, Harvard Pap. Bot. 18: 99. 2013. 9. Matthiola shehbazii Ranjbar & Karami, Nordic J. Bot. doi: 10.1111/j.1756-1051.2013.00326.x, 10. Plocama alshehbazii F. O. Khass., D. Khamr., U. Khuzh. & Achilova, Stapfia 101: 25. 2014. 11. Alshehbazia Salariato & Zuloaga, Kew Bulletin …….. 2015 12. Alshehbzia hauthalii (Gilg & Muschl.) Salariato & Zuloaga 13. Ihsanalshehbazia Tahir Ali & Thines, Taxon 65: 93. 2016. 14. Ihsanalshehbazia granatensis (Boiss. & Reuter) Tahir Ali & Thines, Taxon 65. 93. 2016. 15. Aubrieta alshehbazii Dönmez, Uǧurlu & M.A.Koch, Phytotaxa 299. 104. 2017. 16. Silene shehbazii S.A.Ahmad, Novon 25: 131. 2017. PUBLICATIONS OF IHSAN A. AL-SHEHBAZ 1973 1. Al-Shehbaz, I. A. 1973. The biosystematics of the genus Thelypodium (Cruciferae). Contrib. Gray Herb. 204: 3-148. 1977 2. Al-Shehbaz, I. A. 1977. Protogyny, Cruciferae. Syst. Bot. 2: 327-333. 3. A. R. Al-Mayah & I. A. Al-Shehbaz. 1977. Chromosome numbers for some Leguminosae from Iraq. Bot. Notiser 130: 437-440. 1978 4. Al-Shehbaz, I. A. 1978. Chromosome number reports, certain Cruciferae from Iraq. -
COLLECTION SPECIES from POTENTILLA GENUS Romanian
NATURAL RESOURCES AND SUSTAINABLE DEVELOPMENT, _ 2017 COLLECTION SPECIES FROM POTENTILLA GENUS Crișan Vlad*, Dincă Lucian*, Onet Cristian**, Onet Aurelia** *National Institute for Research and Development in Forestry (INCDS) „Marin Dracea”, 13 Cloșca St., 500040, Brașov, Romania, e-mail: [email protected] **University of Oradea, Faculty of Environmental Protection, 26 Gen. Magheru St., 410048, Oradea, Romania Abstract The present paper reunites the morphological and ecological description of the main species belonging to Potentilla genus present in "Alexandru Beldie" Herbarium from Romanian National Institute for Research and Development in Forestry "Marin Drăcea" (INCDS), Bucharest. Furthermore, the paper systemize the herbarium specimens based on species, harvest year, the place from where they were harvested and the specialist that gathered them. The first part of the article shortly describes the herbarium and its specific, together with a presentation of the material and method used for elaborating this paper. As such, the material that was used is represented by the 276 plates that contain the specimens of 69 species belonging to the Potentilla genus. Besides the description of harvested Potentilla species, the article presents the European map of their harvesting locations, together with a synthetic analysis of their harvesting periods. The paper ends with a series of conclusions regarding the analysis of the Potentilla genus species and specimens present in the herbarium. Key words: herbar, plante, flowers, frunze, Potentilla. INTRODUCTION Romanian National Institute for Research and Development in Forestry "Marin Drăcea" (INCDS) from Bucharest hosts an extremely valuable collection of herbaceous plants. This herbarium is registered in "INDEX HERBARIORUM" which is a guide to the world's herbaria and their staff established since 1935. -
Phylogenetic Position and Generic Limits of Arabidopsis (Brassicaceae)
PHYLOGENETIC POSITION Steve L. O'Kane, Jr.2 and Ihsan A. 3 AND GENERIC LIMITS OF Al-Shehbaz ARABIDOPSIS (BRASSICACEAE) BASED ON SEQUENCES OF NUCLEAR RIBOSOMAL DNA1 ABSTRACT The primary goals of this study were to assess the generic limits and monophyly of Arabidopsis and to investigate its relationships to related taxa in the family Brassicaceae. Sequences of the internal transcribed spacer region (ITS-1 and ITS-2) of nuclear ribosomal DNA, including 5.8S rDNA, were used in maximum parsimony analyses to construct phylogenetic trees. An attempt was made to include all species currently or recently included in Arabidopsis, as well as species suggested to be close relatives. Our ®ndings show that Arabidopsis, as traditionally recognized, is polyphyletic. The genus, as recircumscribed based on our results, (1) now includes species previously placed in Cardaminopsis and Hylandra as well as three species of Arabis and (2) excludes species now placed in Crucihimalaya, Beringia, Olimar- abidopsis, Pseudoarabidopsis, and Ianhedgea. Key words: Arabidopsis, Arabis, Beringia, Brassicaceae, Crucihimalaya, ITS phylogeny, Olimarabidopsis, Pseudoar- abidopsis. Arabidopsis thaliana (L.) Heynh. was ®rst rec- netic studies and has played a major role in un- ommended as a model plant for experimental ge- derstanding the various biological processes in netics over a half century ago (Laibach, 1943). In higher plants (see references in Somerville & Mey- recent years, many biologists worldwide have fo- erowitz, 2002). The intraspeci®c phylogeny of A. cused their research on this plant. As indicated by thaliana has been examined by Vander Zwan et al. Patrusky (1991), the widespread acceptance of A. (2000). Despite the acceptance of A. -
ISTA List of Stabilized Plant Names 7Th Edition
ISTA List of Stabilized Plant Names th 7 Edition ISTA Nomenclature Committee Chair: Dr. M. Schori Published by All rights reserved. No part of this publication may be The Internation Seed Testing Association (ISTA) reproduced, stored in any retrieval system or transmitted Zürichstr. 50, CH-8303 Bassersdorf, Switzerland in any form or by any means, electronic, mechanical, photocopying, recording or otherwise, without prior ©2020 International Seed Testing Association (ISTA) permission in writing from ISTA. ISBN 978-3-906549-77-4 ISTA List of Stabilized Plant Names 1st Edition 1966 ISTA Nomenclature Committee Chair: Prof P. A. Linehan 2nd Edition 1983 ISTA Nomenclature Committee Chair: Dr. H. Pirson 3rd Edition 1988 ISTA Nomenclature Committee Chair: Dr. W. A. Brandenburg 4th Edition 2001 ISTA Nomenclature Committee Chair: Dr. J. H. Wiersema 5th Edition 2007 ISTA Nomenclature Committee Chair: Dr. J. H. Wiersema 6th Edition 2013 ISTA Nomenclature Committee Chair: Dr. J. H. Wiersema 7th Edition 2019 ISTA Nomenclature Committee Chair: Dr. M. Schori 2 7th Edition ISTA List of Stabilized Plant Names Content Preface .......................................................................................................................................................... 4 Acknowledgements ....................................................................................................................................... 6 Symbols and Abbreviations .......................................................................................................................... -
NJ Native Plants - USDA
NJ Native Plants - USDA Scientific Name Common Name N/I Family Category National Wetland Indicator Status Thermopsis villosa Aaron's rod N Fabaceae Dicot Rubus depavitus Aberdeen dewberry N Rosaceae Dicot Artemisia absinthium absinthium I Asteraceae Dicot Aplectrum hyemale Adam and Eve N Orchidaceae Monocot FAC-, FACW Yucca filamentosa Adam's needle N Agavaceae Monocot Gentianella quinquefolia agueweed N Gentianaceae Dicot FAC, FACW- Rhamnus alnifolia alderleaf buckthorn N Rhamnaceae Dicot FACU, OBL Medicago sativa alfalfa I Fabaceae Dicot Ranunculus cymbalaria alkali buttercup N Ranunculaceae Dicot OBL Rubus allegheniensis Allegheny blackberry N Rosaceae Dicot UPL, FACW Hieracium paniculatum Allegheny hawkweed N Asteraceae Dicot Mimulus ringens Allegheny monkeyflower N Scrophulariaceae Dicot OBL Ranunculus allegheniensis Allegheny Mountain buttercup N Ranunculaceae Dicot FACU, FAC Prunus alleghaniensis Allegheny plum N Rosaceae Dicot UPL, NI Amelanchier laevis Allegheny serviceberry N Rosaceae Dicot Hylotelephium telephioides Allegheny stonecrop N Crassulaceae Dicot Adlumia fungosa allegheny vine N Fumariaceae Dicot Centaurea transalpina alpine knapweed N Asteraceae Dicot Potamogeton alpinus alpine pondweed N Potamogetonaceae Monocot OBL Viola labradorica alpine violet N Violaceae Dicot FAC Trifolium hybridum alsike clover I Fabaceae Dicot FACU-, FAC Cornus alternifolia alternateleaf dogwood N Cornaceae Dicot Strophostyles helvola amberique-bean N Fabaceae Dicot Puccinellia americana American alkaligrass N Poaceae Monocot Heuchera americana -
The Evolutionary Fate of Rpl32 and Rps16 Losses in the Euphorbia Schimperi (Euphorbiaceae) Plastome Aldanah A
www.nature.com/scientificreports OPEN The evolutionary fate of rpl32 and rps16 losses in the Euphorbia schimperi (Euphorbiaceae) plastome Aldanah A. Alqahtani1,2* & Robert K. Jansen1,3 Gene transfers from mitochondria and plastids to the nucleus are an important process in the evolution of the eukaryotic cell. Plastid (pt) gene losses have been documented in multiple angiosperm lineages and are often associated with functional transfers to the nucleus or substitutions by duplicated nuclear genes targeted to both the plastid and mitochondrion. The plastid genome sequence of Euphorbia schimperi was assembled and three major genomic changes were detected, the complete loss of rpl32 and pseudogenization of rps16 and infA. The nuclear transcriptome of E. schimperi was sequenced to investigate the transfer/substitution of the rpl32 and rps16 genes to the nucleus. Transfer of plastid-encoded rpl32 to the nucleus was identifed previously in three families of Malpighiales, Rhizophoraceae, Salicaceae and Passiforaceae. An E. schimperi transcript of pt SOD-1- RPL32 confrmed that the transfer in Euphorbiaceae is similar to other Malpighiales indicating that it occurred early in the divergence of the order. Ribosomal protein S16 (rps16) is encoded in the plastome in most angiosperms but not in Salicaceae and Passiforaceae. Substitution of the E. schimperi pt rps16 was likely due to a duplication of nuclear-encoded mitochondrial-targeted rps16 resulting in copies dually targeted to the mitochondrion and plastid. Sequences of RPS16-1 and RPS16-2 in the three families of Malpighiales (Salicaceae, Passiforaceae and Euphorbiaceae) have high sequence identity suggesting that the substitution event dates to the early divergence within Malpighiales.