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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. -
National List of Vascular Plant Species That Occur in Wetlands 1996
National List of Vascular Plant Species that Occur in Wetlands: 1996 National Summary Indicator by Region and Subregion Scientific Name/ North North Central South Inter- National Subregion Northeast Southeast Central Plains Plains Plains Southwest mountain Northwest California Alaska Caribbean Hawaii Indicator Range Abies amabilis (Dougl. ex Loud.) Dougl. ex Forbes FACU FACU UPL UPL,FACU Abies balsamea (L.) P. Mill. FAC FACW FAC,FACW Abies concolor (Gord. & Glend.) Lindl. ex Hildebr. NI NI NI NI NI UPL UPL Abies fraseri (Pursh) Poir. FACU FACU FACU Abies grandis (Dougl. ex D. Don) Lindl. FACU-* NI FACU-* Abies lasiocarpa (Hook.) Nutt. NI NI FACU+ FACU- FACU FAC UPL UPL,FAC Abies magnifica A. Murr. NI UPL NI FACU UPL,FACU Abildgaardia ovata (Burm. f.) Kral FACW+ FAC+ FAC+,FACW+ Abutilon theophrasti Medik. UPL FACU- FACU- UPL UPL UPL UPL UPL NI NI UPL,FACU- Acacia choriophylla Benth. FAC* FAC* Acacia farnesiana (L.) Willd. FACU NI NI* NI NI FACU Acacia greggii Gray UPL UPL FACU FACU UPL,FACU Acacia macracantha Humb. & Bonpl. ex Willd. NI FAC FAC Acacia minuta ssp. minuta (M.E. Jones) Beauchamp FACU FACU Acaena exigua Gray OBL OBL Acalypha bisetosa Bertol. ex Spreng. FACW FACW Acalypha virginica L. FACU- FACU- FAC- FACU- FACU- FACU* FACU-,FAC- Acalypha virginica var. rhomboidea (Raf.) Cooperrider FACU- FAC- FACU FACU- FACU- FACU* FACU-,FAC- Acanthocereus tetragonus (L.) Humm. FAC* NI NI FAC* Acanthomintha ilicifolia (Gray) Gray FAC* FAC* Acanthus ebracteatus Vahl OBL OBL Acer circinatum Pursh FAC- FAC NI FAC-,FAC Acer glabrum Torr. FAC FAC FAC FACU FACU* FAC FACU FACU*,FAC Acer grandidentatum Nutt. -
Genus Oenothera)
1046 Asian Pac J Trop Biomed 2017; 7(11): 1046–1054 Contents lists available at ScienceDirect Asian Pacific Journal of Tropical Biomedicine journal homepage: www.elsevier.com/locate/apjtb Review article https://doi.org/10.1016/j.apjtb.2017.10.004 An updated review on pharmacological activities and phytochemical constituents of evening primrose (genus Oenothera) Rebecca Munir1, Nabil Semmar2, Muhammad Farman1*, Naseem Saud Ahmad3 1Department of Chemistry, Quaid-i-Azam University, Islamabad 45320, Pakistan 2Laboratory of Bioinformatics, Biomathematics and Biostatistics, Pasteur Institute of Tunis, University of Tunis El Manar, Tunisia 3Department of Pharmacology, University of Health Sciences, Lahore, Pakistan ARTICLE INFO ABSTRACT Article history: Genus Oenothera includes medicinal plants that are distributed throughout the world and Received 22 Aug 2017 are known since ancient times. Popular indications of different species of this genus Received in revised form 19 Sep 2017 include treatment of inflammations, diabetes, microbial infections, ulcers, tumors, kidney Accepted 13 Oct 2017 and liver problems. The plants of this genus are a botanical source for various pharma- Available online 23 Oct 2017 ceutically active components like sterols, alkaloids, phenolic acids, flavonoids, triterpe- noids, saponins, biflavonols and tocopherols. This review article is a compilation of chemical composition and biological activities of the various species of the genus Keywords: Oenothera. Oenothera Medicinal plants Chemical composition Biological activities 1. Introduction shaped white, pink, yellow and red flowers, and most are fragrant [2]. Herbal plants play a significant role in the life of humans as The plants owned to Oenothera have a wide range of me- they are being used in different fields such as pharmacology, dicinal properties that prompted us to compile a review article on cosmetics, perfumery, nutraceuticals, beverages and dying in- this particular genus. -
Oenothera, a Unique Model to Study the Role of Plastids in Speciation
Oenothera, a unique model to study the role of plastids in speciation Dissertation der Fakultät für Biologie der Ludwig-Maximilians-Universität München vorgelegt von Stephan Greiner am 15. Mai 2008 Erstgutachter: Professor Reinhold G. Herrmann Zweitgutachter: Professor Wolfgang Stephan Tag der mündlichen Prüfung: 19. Juni 2008 Table of Contents Table of Contents 1. Introduction ...................................................................................................................... 1 1.1. Eukaryotic genomes are integrated and compartmentalized ...................................... 1 1.2. Dobzhansky-Muller incompatibilities and asymmetric hybridization barriers .......... 2 1.2.1. The model of Dobzhansky-Muller incompatibility .............................................. 4 1.2.2. “Speciation genes” have not yet been identified for PGI ..................................... 5 1.3. Hybridization barriers formed by plastids .................................................................. 6 1.4. The occurrence of PGI in natural populations is underestimated ............................ 10 1.5. Physiology and cell biology of PGI ......................................................................... 14 1.5.1. Albinotic phenotypes of PGI .............................................................................. 15 1.5.2. PGI phenotypes with affected cell growth and function .................................... 15 1.6. Oenothera as a molecular model to investigate PGI ................................................ 17 -
Philosophical and Historical Reflections on the Artificial-Natural Distinction in the Life Sciences ! ! by ! S
! DENATURING NATURE ! Philosophical and Historical Reflections on the Artificial-Natural Distinction in the Life Sciences ! ! by ! S. Andrew Inkpen ! B.Sc. Saint Mary’s University 2008 ! ! ! ! ! A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF ! Doctor of Philosophy ! in ! The Faculty of Graduate and Postdoctoral Studies ! (Philosophy) ! ! ! ! ! THE UNIVERSITY OF BRITISH COLUMBIA (Vancouver) ! August 2014 ! © S. Andrew Inkpen, 2014 ! ! ABSTRACT ! ! The philosopher Georges Canguilhem observed that the “physician’s thought and activity are incomprehensible without the concepts of the normal and the pathological.” I argue similarly regarding the biologist, only it is “the artificial” and “the natural” that are indispensable. Whether it is their objects of study, the methods used to investigate those objects, or even fellow researchers, biologists have habitually classified aspects of their discipline in a way that reflects the artificial-natural distinction. Why this way of classifying? What purpose does it serve? What principles guide its application? With what repercussions? Tracing the transformation of these concepts through a series of historical episodes, I explore the reasons why biologists use this distinction and how it has influenced the practices and directions of certain biological fields—specifically evolutionary biology and ecology. The argument of this dissertation is that in biology decisions concerning the choice and evaluation of experimental and evidential practices, objects of study, and even assessments of scientific personas betray the artificial-natural distinction. Invocations of this distinction, like the normal-pathological, code normative contentions about proper biological practice. “The natural,” I argue, often functions as an epistemic authority. The methodology I employ in this dissertation is conceptual and historical. -
Mapping of Genomes and Plastomes of Subsection Oenothera with Molecular Marker Technologies
Mapping of genomes and plastomes of subsection Oenothera with molecular marker technologies Dissertation zur Erlangung des Doktorgrades der Fakultät für Biologie der Ludwig-Maximilians-Universität München vorgelegt von Uwe Rauwolf aus Stuttgart, Deutschland München Juni 2008 1. Gutachter: Prof. Dr. Reinhold G. Herrmann 2. Gutachter: Prof. Dr. Günther Heubl Tag der mündlichen Prüfung: 11.08.2008 “Nothing in Biology makes sense, except in the light of evolution.” Theodosius Dobzhansky (1973) This dissertation is dedicated to my father, † 21.01.1991 Franz Willi Rauwolf ABBREVIATIONS ABI Applied Biosystems AFLP amplified fragment length polymorphism am ammophila APS ammonium persulphate ATP adenosine 5´-triphosphate atro atrovirens biM biennis München BLAST basic local alignment search tool bp base pair(s) BSA Bovine Serum Albumin CAPS cleavable amplified polymorphic sequence CIAP calf intestinal alkaline phosphatase CMS cytoplasmatic male sterility Col Colmar (chicaginensis Colmar) DAPI 4’,6-Diamidino 2-phenyindole DM Dobzhansky-Muller DMI Dobzhansky-Muller incompatibility DNA deoxyribonucleic acid DSB Double Strand Break DTT Dithiothreitol dV de Vries EDTA ethylenediamine-tetraacetic acid e.g. exempli gratia EST expressed sequence tag(s) et al. et alia EtOH ethanol F1 filial generation 1 F2 filial generation 2 G Grado (suaveolens Grado) g gravitation force; gram h haplo(type) h hour(s) -IV- Hz Hertz i.e. id est joh johansen kb (= kbp) kilo base pairs kV kilo volt lam lamarckiana LB medium Luria Bertani medium LOD logarithm of odds M molar mRNA messenger RNA ms millisecond µE microeinstein μg microgram μl microlitre N/A not applicable NaAc sodium acetate ng nanogram NPQ non-photochemical quenching Oe Oenothera P700 photosystem I primary electron donor chlorophyll a p.a. -
Chemical and Biological Significance of Oenothein B and Related
molecules Review Chemical and Biological Significance of Oenothein B and Related Ellagitannin Oligomers with Macrocyclic Structure Takashi Yoshida 1,2, Morio Yoshimura 1 and Yoshiaki Amakura 1,* 1 College of Pharmaceutical Sciences, Matsuyama University, 4-2 Bunkyo-cho, Matsuyama, Ehime 790-8578, Japan; [email protected] (T.Y.); [email protected] (M.Y.) 2 Okayama University, Okayama 701-1152, Japan * Correspondence: [email protected]; Tel.: +81-89-925-7111 Received: 5 February 2018; Accepted: 26 February 2018; Published: 2 March 2018 Abstract: In 1990, Okuda et al. reported the first isolation and characterization of oenothein B, a unique ellagitannin dimer with a macrocyclic structure, from the Oenothera erythrosepala leaves. Since then, a variety of macrocyclic analogs, including trimeric–heptameric oligomers have been isolated from various medicinal plants belonging to Onagraceae, Lythraceae, and Myrtaceae. Among notable in vitro and in vivo biological activities reported for oenothein B are antioxidant, anti-inflammatory, enzyme inhibitory, antitumor, antimicrobial, and immunomodulatory activities. Oenothein B and related oligomers, and/or plant extracts containing them have thus attracted increasing interest as promising targets for the development of chemopreventive agents of life-related diseases associated with oxygen stress in human health. In order to better understand the significance of this type of ellagitannin in medicinal plants, this review summarizes (1) the structural characteristics of oenothein B and related dimers; (2) the oxidative metabolites of oenothein B up to heptameric oligomers; (3) the distribution of oenotheins and other macrocyclic analogs in the plant kingdom; and (4) the pharmacological activities hitherto documented for oenothein B, including those recently found by our laboratory. -
Pteridophyta and Spermatophyta)
4.2 LISTA DAS PLANTAS VASCULARES (Pteridophyta e Spermatophyta) LIST OF VASCULAR PLANTS (Pteridophyta and Spermatophyta) Autores (Authors) Luís Silva1, Nuno Pinto,1 Bob Press2, Fred Rumsey2, Mark Carine2, Sally Henderson2 & Erik Sjögren3 1 Departamento de Biologia, Universidade dos Açores, Rua da Mãe de Deus, PT 9501-801 Ponta Delgada, Açores, Portugal. e-mail: [email protected]; [email protected]. 2 Department of Botany, Natural History Museum, Cromwell Road, London SW7 5BD, UK. e-mail: [email protected]; [email protected]; [email protected]; [email protected]. 3 University of Uppsala. Evolutionary Biology Centre. Department of Plant Ecology. Villavagen, 14. SE-752 36 Sweden. e-mail: [email protected]. 131 Notas explicativas Explanatory notes A lista das plantas vasculares dos Açores é baseada The list of the Azorean vascular plants is based em toda a literatura conhecida, incluindo as refe- on all known published literature, including older rências mais antigas (i.e. Seubert & Hochstetter references (i.e. Seubert & Hochstetter 1843; 1843; Trelease 1897; Palhinha 1966), a Flora Trelease 1897; Palhinha 1966), the Flora Europaea Europaea (Tutin et al. 1964-1980), as publicações (Tutin et al. 1964-1980), the publications by de Franco (1971, 1984), Franco & Afonso (1994, Franco (1971, 1984) and Franco & Afonso (1994, 1998) e ainda em publicações mais recentes, em 1998), and also more recent publications, namely particular, as de Schäfer (2002, 2003). those from Schäfer (2002, 2003). No que diz respeito aos dados não publicados, Unpublished data were also used, namely from foram usadas várias fontes, nomeadamente os re- records at the Natural History Museum, and from gistos do Museu de História Natural e ainda obser- field observations (Silva 2001). -
Philosophical and Historical Reflections on the Artificial-Natural Distinction in the Life Sciences ! ! by ! S
! DENATURING NATURE ! Philosophical and Historical Reflections on the Artificial-Natural Distinction in the Life Sciences ! ! by ! S. Andrew Inkpen ! B.Sc. Saint Mary’s University 2008 ! ! ! ! ! A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF ! Doctor of Philosophy ! in ! The Faculty of Graduate and Postdoctoral Studies ! (Philosophy) ! ! ! ! ! THE UNIVERSITY OF BRITISH COLUMBIA (Vancouver) ! August 2014 ! © S. Andrew Inkpen, 2014 ! ! ABSTRACT ! ! The philosopher Georges Canguilhem observed that the “physician’s thought and activity are incomprehensible without the concepts of the normal and the pathological.” I argue similarly regarding the biologist, only it is “the artificial” and “the natural” that are indispensable. Whether it is their objects of study, the methods used to investigate those objects, or even fellow researchers, biologists have habitually classified aspects of their discipline in a way that reflects the artificial-natural distinction. Why this way of classifying? What purpose does it serve? What principles guide its application? With what repercussions? Tracing the transformation of these concepts through a series of historical episodes, I explore the reasons why biologists use this distinction and how it has influenced the practices and directions of certain biological fields—specifically evolutionary biology and ecology. The argument of this dissertation is that in biology decisions concerning the choice and evaluation of experimental and evidential practices, objects of study, and even assessments of scientific personas betray the artificial-natural distinction. Invocations of this distinction, like the normal-pathological, code normative contentions about proper biological practice. “The natural,” I argue, often functions as an epistemic authority. The methodology I employ in this dissertation is conceptual and historical. -
Catalogue of the Naturalized Flora of Taiwan
Taiwania, 49(1):16-31, 2004 Catalogue of the Naturalized Flora of Taiwan Shan-Huah Wu(1,3), Chang-Fu Hsieh(2), and Marcel Rejmánek(1) (Manuscript received 14 October, 2003; accepted 18 November, 2003) ABSTRACT: This study was conducted in years 2000 to 2003 to compile a comprehensive list of naturalized species with background information, including origins, life forms, habits, usages, year of the first collection, and status. Major herbaria (TAI, HAST, TAIF, and NCKU) were visited to examine specimen records. Relevant publications and reliable websites and many other resources were also examined extensively for background information. Total 341 species in 222 genera and 60 families were documented as naturalized in Taiwan, representing 7.9% of the local flora. Besides, 25 species were considered as possibly naturalized due to insufficient evidences. A large portion (90.6%) of species reported here, were reported as “weeds” in other countries. Almost a half of the naturalized species (48.3%) were introduced from Americas. KEYWORDS: Naturalized plant, Plant invasions, List,Taiwan. INTRODUCTION Despite the recent recognition of the impacts caused by invasive plants worldwide (Mooney and Hobbs, 2000; Vitousek et al., 1997), there are still many regions in the world where basic information on naturalized plant taxa and plant invasions is only anecdotal or completely lacking, e.g. Asia and neighboring regions (Corlett, 1988; Meyer, 2000; Turner, 1995; Enmoto, 1999; Pandey, 2000). In Taiwan, although occasional attention has been paid to the naturalized plants (Chen and Wu 1997; Peng et al. 1998a, 1998b; Peng and Yang, 1998; Chen et al., 1999; Kuoh and Chen, 2000; Chen and Wu, 2001; Yang, 2001; Yang and Peng, 2001), comprehensive studies on invasive species and plant invasions are still missing. -
New Zealand Naturalised Vascular Plant Checklist
NEW ZEALAND NATURALISED VASCULAR PLANT CHECKLIST Clayson Howell; ISBN 0-473-11306-6 John W.D. Sawyer New Zealand Plant Conservation Network November 2006 9 780473 113063 New Zealand naturalised vascular plant checklist November 2006 Clayson J. Howell, John W.D. Sawyer New Zealand Plant Conservation Network P.O. Box 16-102 Wellington New Zealand 6242 E-mail: [email protected] www.nzpcn.org.nz Cover photos (by Jeremy Rolfe): Selaginella kraussiana (Lycophytes), Cestrum elegans (Dicot. trees & shrubs), Cyperus eragrostis (Monocot. herbs: Sedges), Cerastium glomeratum (Dicot. herbs other than composites), Dipogon lignosus (Dicot lianes), Berberis darwinii (Dicot. trees & shrubs), Lonicera japonica (Dicot. lianes), Bomarea caldasii (Monocot. lianes), Pinus radiata (Gymnosperm trees & shrubs), Lilium formosanum (Monocot. herbs other than grasses, orchids, rushes, sedges), Poa annua (Monocot. herbs: Grasses), Clematis vitalba (Dicot. lianes), Adiantum raddianum (Ferns) Main photo: Senecio diaschides (Dicot herbs: Composites). Title page: Asparagus scandens seedling in kauri forest. © Clayson J. Howell, John W.D. Sawyer 2006 ISBN-10: 0-473-12300-2 ISBN-13: 978-0-473-12300-0 Published by: New Zealand Plant Conservation Network P.O. Box 16-102 Wellington 6242 New Zealand E-mail: [email protected] www.nzpcn.org.nz CONTENTS Introduction 1 New Zealand adventive flora – Summary statistics 2 Naturalised plant records in the Flora of New Zealand 2 Naturalised plant checklists in the New Zealand Journal of Botany 2 Species outside Flora or checklists 2 Acknowledgements 4 Bibliography 4 New Zealand naturalised vascular plant checklist – alphabetical 6 iii Cortaderia selloana, one of two species of pampas that are fully naturalised in New Zealand. -
ONAGRACEAE 1. LUDWIGIA Linnaeus, Sp
ONAGRACEAE 柳叶菜科 liu ye cai ke Chen Jiarui (陈家瑞 Chen Chia-jui)1; Peter C. Hoch2, Peter H. Raven2, David E. Boufford3, Warren L. Wagner4 Annual or perennial herbs, or shrubs, rarely trees to 30 m tall, often with epidermal oil cells, usually with internal phloem. Leaves simple, spirally arranged, opposite, or occasionally whorled, entire or toothed to pinnatifid; stipules present and usually caducous, or absent. Flowers perfect and hermaphroditic or occasionally unisexual, actinomorphic or zygomorphic, (2–)4(–7)- merous, axillary, in leafy spikes or racemes or solitary, or occasionally in panicles, all but Ludwigia with distinct floral tube, nectariferous within. Sepals green or colored, valvate. Petals as many as sepals or rarely absent, variously colored, imbricate or convolute and occasionally clawed. Stamens as many as sepals in one series or 2 × as many as sepals in 2 series [in Lopezia Cavanil- les reduced to 2 or 1 plus 1 sterile staminode]; anthers versatile or basifixed, dithecal, sometimes cross-partitioned, opening by longitudinal slits; pollen grains almost always united by viscin threads, shed as monads, tetrads, or polyads. Ovary inferior, with as many carpels and locules as sepals, septa sometimes thin or absent at maturity; placentation axile or parietal, ovules 1 to many per locule, in 1 or several rows or clustered, anatropous, bitegmic; style 1; stigma with as many lobes as sepals or clavate to globose. Fruit a loculicidal capsule or indehiscent nut or berry. Seeds small, smooth or variously sculptured, sometimes with a coma [or wing], with straight oily embryo, endosperm lacking. Seventeen genera and ca. 650 species: widespread in temperate and subtropical areas, but best represented in W North America; six genera (two introduced), 64 species (11 endemic, 11 introduced), and five natural hybrids (two endemic) in China.