Polygala Senega (Seneca Snakeroot)
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Biological Control Prospects for Polygala
72 Plant Protection Quarterly Vol.26(2) 2011 Mechanical and chemical control tech- niques are utilized to suppress P. myrtifo- Phytophagous organisms associated with the woody lia, but are generally only successful when shrub Polygala myrtifolia (Polygalaceae) and their applied to small areas where regular fol- low-up treatments can be implemented. potential for classical biological control in Australia In Australia, few phytophagous arthro- pods occur on P. myrtifolia, and herbivory Robin J. AdairA,D, Stefan NeserB and Val StajsicC damage is low to negligible. Low herbivo- A Department of Primary Industries, Bioprotection Research Division, ry pressure in Australia may contribute to PO Box 48, Frankston, Victoria 3199, Australia. the success of P. myrtifolia as an environ- B Plant Protection Research Institute, Agricultural Research Council, mental weed. In contrast, phytophagous species can cause substantial damage to Private Bag, X134, Pretoria 0001, South Africa. C P. myrtifolia in South Africa, and several National Herbarium of Victoria, Royal Botanic Gardens Melbourne, species have potential for classical biolog- Birdwood Avenue, South Yarra, Victoria 3141, Australia. ical control (Adair and Neser 1996). Al- D LaTrobe University, Bundoora, Victoria 3086, Australia. though P. myrtifolia has not been formally accepted as a target for biological control in Australia, this form of suppression is considered the only effective long-term Summary management option. Coastal ecosystems in southern Australia in Adelaide in 1845 (Carter et al. 1990). In this paper, the phytophagous biota have been invaded by the South African The first presumed wild collections of associated with P. myrtifolia and their po- shrub Polygala myrtifolia L. (Polyga- P. -
Polygala Retiefiana (Polygalaceae), a New Species Described from South Africa
Phytotaxa 117 (1): 30–34 (2013) ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2013 Magnolia Press Correspondence ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.117.1.4 Polygala retiefiana (Polygalaceae), a new species described from South Africa JORGE PAIVA1, ESTRELA FIGUEIREDO1,2 & GIDEON F. SMITH1,3,4 1Centre for Functional Ecology, Departamento de Ciências da Vida, Universidade de Coimbra, 3001-455 Coimbra, Portugal. 2Department of Botany, P.O. Box 77000, Nelson Mandela Metropolitan University, Port Elizabeth, 6031 South Africa. [email protected] (corresponding author) 3Office of the Chief Director: Biosystematics Research & Biodiversity Collections, South African National Biodiversity Institute, Private Bag X101, Pretoria, 0001 South Africa. 4H.G.W.J. Schweickerdt Herbarium, Department of Plant Science, University of Pretoria, Pretoria, 0002 South Africa. Abstract A new species of Polygala (Polygalaceae), P. retiefiana, is described from the KwaZulu-Natal and Free State provinces of South Africa. It is endemic to the country. Key words: plant taxonomy, biodiversity, Polygalaceae, Polygala retiefiana, endemic, South Africa With the order Polygalales no longer accepted, the Polygalaceae belong now to the order Fabales, the circumscription of which (Chase et al. 1993) includes four families: Fabaceae, Polygalaceae, Quillajaceae and Saurianaceae. These families have as common characteristic the monosymmetric flowers (Tucker 2003) where one of the petals, or two united petals, form a keel (carina) which covers the androecium and gynoecium. This group of plants with papilionaceous or pseudo-papilionaceous flowers is well-characterised both molecularly (APG III 2009) and ontogenically (Bello et al. 2010). Interfamilial relationships and patterns of floral evolution were also found between these four families (Bello et al. -
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 -
Reassessment of Variation Within Polygala Cruciata Sensu Lato (Polygalaceae)
Sorrie, B.A. and A.S. Weakley. 2017. Reassessment of variation within Polygala cruciata sensu lato (Polygalaceae). Phytoneuron 2017-37: 1–9. Published 1 June 2017. ISSN 2153 733X REASSESSMENT OF VARIATION WITHIN POLYGALA CRUCIATA SENSU LATO (POLYGALACEAE) BRUCE A. SORRIE AND ALAN S. WEAKLEY UNC Herbarium (NCU), North Carolina Botanical Garden University of North Carolina at Chapel Hill Chapel Hill, North Carolina 27599-3280 ABSTRACT Herbarium research confirms the presence of two distinct entities within Polygala cruciata sensu lato, each of which we treat as species. Polygala cruciata is nearly endemic to the Coastal Plain, with local disjunctions inland, whereas P. aquilonia is northern with populations southward in the Appalachian Mountains and southward along the coast to Virginia. Several eastern North American floras have distinguished two intraspecific entities within Polygala cruciata L. Fernald (1950) and Weakley (2015) have recognized these as varieties –– P. cruciata var. cruciata and var. aquilonia Fernald & Schubert. A few other floras (e.g., Mohlenbrock 2014), in the range of only one of the varieties, specify that variety but do not provide a rationale. Haines (2011) treated two entities at subspecific rank (a nom. illeg . because of failure to cite the basionym publication). The characters used by Fernald & Schubert (1948) are leaf width, width of the inflorescence, and length of the peduncle. These treatments appear to rely strictly on Fernald & Schubert (1948), with no evidence of new and independent assessments of the -
Evolution of Angiosperm Pollen. 7. Nitrogen-Fixing Clade1
Evolution of Angiosperm Pollen. 7. Nitrogen-Fixing Clade1 Authors: Jiang, Wei, He, Hua-Jie, Lu, Lu, Burgess, Kevin S., Wang, Hong, et. al. Source: Annals of the Missouri Botanical Garden, 104(2) : 171-229 Published By: Missouri Botanical Garden Press URL: https://doi.org/10.3417/2019337 BioOne Complete (complete.BioOne.org) is a full-text database of 200 subscribed and open-access titles in the biological, ecological, and environmental sciences published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Complete website, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/terms-of-use. Usage of BioOne Complete content is strictly limited to personal, educational, and non - commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. Downloaded From: https://bioone.org/journals/Annals-of-the-Missouri-Botanical-Garden on 01 Apr 2020 Terms of Use: https://bioone.org/terms-of-use Access provided by Kunming Institute of Botany, CAS Volume 104 Annals Number 2 of the R 2019 Missouri Botanical Garden EVOLUTION OF ANGIOSPERM Wei Jiang,2,3,7 Hua-Jie He,4,7 Lu Lu,2,5 POLLEN. 7. NITROGEN-FIXING Kevin S. Burgess,6 Hong Wang,2* and 2,4 CLADE1 De-Zhu Li * ABSTRACT Nitrogen-fixing symbiosis in root nodules is known in only 10 families, which are distributed among a clade of four orders and delimited as the nitrogen-fixing clade. -
SENEGA SNAKEROOT Over Harvesting in One Area
BUYING REQUIREMENTS (THIS IS INTENDED TO QUALITY CONTROL: NON-TIMBER PROVIDE GENERAL STANDARDS. REQUIREMENTS FOREST MAY VARY FROM BUYER TO BUYER. PLEASE CON- Handling: PRODUCTS FIRM WITH YOUR BUYER BEFORE HARVESTING): • Wash hands before harvesting or handling INFORMATION • Green senega root– must be brought in a roots. BROCHURE clean container, paper bag, paper box or Harvesting: new poly-woven rice bag. (FROM HARVESTING PRACTICES) • Harvesting senega root can be done as • Do not store green or dry senega root in soon as the frost leaves the ground and a plastic bag. the plant is recognizable • Producers must have a Wild Harvesters SENEGA • The best quality senega root can be Association Membership Card. SNAKEROOT harvested in the fall • General harvest area. • No foreign smell (ex: gas, oil) Drying process: • No foreign material (ex: Different kinds of • Producer must have a drying shed or a bark, dirt, rocks) place that can be inspected • No mould. • Spread senega root on screens in layers All bags, boxes and containers will be • Room must have heat source inspected to determine if product • Use a fan to move air around senega root meets NFDC specifications. • Drying process takes 5 to 8 days in a well PRICING: ventilated dryer. • Call NFDC prior to shipping or traveling to buying depot. Storage Technique: • Product should be stored in a clean poly woven rice bag, paper bag, paper box, or clean container. • Dirty containers will not be accepted and the product in it maybe rejected • Do not store in a shed that has been used for storing gas and oil. -
International Journal of Pharmacy & Life Sciences
Review Article [Sharma et al., 6(1): Jan., 2015:4202-4208] CODEN (USA): IJPLCP ISSN: 0976-7126 INTERNATIONAL JOURNAL OF PHARMACY & LIFE SCIENCES (Int. J. of Pharm. Life Sci.) Ethnopharmacological attributes of Polygala senega Linn. Gaurav Sharma*, Alkesh Jhade, Sapna Malviya and Anil Kharia Modern Institute of Pharmaceutical Sciences, Indore, (MP) - India Abstract India has about 45000 plant species, many of them claimed to possess medicinal properties. Medicinal herbs act as a potential source of therapeutic aid and it play significant role in health system all over the world for both humans and animals. Polygala senega Linn is species of a flowering plant in the Polygalaceae Family .The plant has been referred to as a marvel plant because every part of it has been found to be of medicinal magnitude. The present paper aims to review various plant species of Polygala from Indian origin and their constituents, which have been used in the traditional system of medicine to exhibit Hypoglycemic, Anticancer, CNS depressant, Hypolipidaemic and Antifungal activity. Key-Words: Polygala senega , Hypoglycemic , Anticancer activity Introduction Herbal medicine is the oldest health care known to a But some old foliage can have branch stems. A mature mankind. An herb has been used to all cultures thought plant has stems upward from hard woody rootstock that out history. It is an integral part of development of spread horizontally. The lance shaped leaves are civilization primitive man observed and appreciated the alternately arranged. They are mainly grown in great diversity of plants available to him. They summer season at India, and complete their life cycle observed that about 74% of 119 plant-derived in 4-5 month self pollination. -
Species List For: Valley View Glades NA 418 Species
Species List for: Valley View Glades NA 418 Species Jefferson County Date Participants Location NA List NA Nomination and subsequent visits Jefferson County Glade Complex NA List from Gass, Wallace, Priddy, Chmielniak, T. Smith, Ladd & Glore, Bogler, MPF Hikes 9/24/80, 10/2/80, 7/10/85, 8/8/86, 6/2/87, 1986, and 5/92 WGNSS Lists Webster Groves Nature Study Society Fieldtrip Jefferson County Glade Complex Participants WGNSS Vascular Plant List maintained by Steve Turner Species Name (Synonym) Common Name Family COFC COFW Acalypha virginica Virginia copperleaf Euphorbiaceae 2 3 Acer rubrum var. undetermined red maple Sapindaceae 5 0 Acer saccharinum silver maple Sapindaceae 2 -3 Acer saccharum var. undetermined sugar maple Sapindaceae 5 3 Achillea millefolium yarrow Asteraceae/Anthemideae 1 3 Aesculus glabra var. undetermined Ohio buckeye Sapindaceae 5 -1 Agalinis skinneriana (Gerardia) midwestern gerardia Orobanchaceae 7 5 Agalinis tenuifolia (Gerardia, A. tenuifolia var. common gerardia Orobanchaceae 4 -3 macrophylla) Ageratina altissima var. altissima (Eupatorium rugosum) white snakeroot Asteraceae/Eupatorieae 2 3 Agrimonia pubescens downy agrimony Rosaceae 4 5 Agrimonia rostellata woodland agrimony Rosaceae 4 3 Allium canadense var. mobilense wild garlic Liliaceae 7 5 Allium canadense var. undetermined wild garlic Liliaceae 2 3 Allium cernuum wild onion Liliaceae 8 5 Allium stellatum wild onion Liliaceae 6 5 * Allium vineale field garlic Liliaceae 0 3 Ambrosia artemisiifolia common ragweed Asteraceae/Heliantheae 0 3 Ambrosia bidentata lanceleaf ragweed Asteraceae/Heliantheae 0 4 Ambrosia trifida giant ragweed Asteraceae/Heliantheae 0 -1 Amelanchier arborea var. arborea downy serviceberry Rosaceae 6 3 Amorpha canescens lead plant Fabaceae/Faboideae 8 5 Amphicarpaea bracteata hog peanut Fabaceae/Faboideae 4 0 Andropogon gerardii var. -
Pollen and Stamen Mimicry: the Alpine Flora As a Case Study
Arthropod-Plant Interactions DOI 10.1007/s11829-017-9525-5 ORIGINAL PAPER Pollen and stamen mimicry: the alpine flora as a case study 1 1 1 1 Klaus Lunau • Sabine Konzmann • Lena Winter • Vanessa Kamphausen • Zong-Xin Ren2 Received: 1 June 2016 / Accepted: 6 April 2017 Ó The Author(s) 2017. This article is an open access publication Abstract Many melittophilous flowers display yellow and Dichogamous and diclinous species display pollen- and UV-absorbing floral guides that resemble the most com- stamen-imitating structures more often than non-dichoga- mon colour of pollen and anthers. The yellow coloured mous and non-diclinous species, respectively. The visual anthers and pollen and the similarly coloured flower guides similarity between the androecium and other floral organs are described as key features of a pollen and stamen is attributed to mimicry, i.e. deception caused by the flower mimicry system. In this study, we investigated the entire visitor’s inability to discriminate between model and angiosperm flora of the Alps with regard to visually dis- mimic, sensory exploitation, and signal standardisation played pollen and floral guides. All species were checked among floral morphs, flowering phases, and co-flowering for the presence of pollen- and stamen-imitating structures species. We critically discuss deviant pollen and stamen using colour photographs. Most flowering plants of the mimicry concepts and evaluate the frequent evolution of Alps display yellow pollen and at least 28% of the species pollen-imitating structures in view of the conflicting use of display pollen- or stamen-imitating structures. The most pollen for pollination in flowering plants and provision of frequent types of pollen and stamen imitations were pollen for offspring in bees. -
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY BIBLIOGRAPHY Ackerfield, J., and J. Wen. 2002. A morphometric analysis of Hedera L. (the ivy genus, Araliaceae) and its taxonomic implications. Adansonia 24: 197-212. Adams, P. 1961. Observations on the Sagittaria subulata complex. Rhodora 63: 247-265. Adams, R.M. II, and W.J. Dress. 1982. Nodding Lilium species of eastern North America (Liliaceae). Baileya 21: 165-188. Adams, R.P. 1986. Geographic variation in Juniperus silicicola and J. virginiana of the Southeastern United States: multivariant analyses of morphology and terpenoids. Taxon 35: 31-75. ------. 1995. Revisionary study of Caribbean species of Juniperus (Cupressaceae). Phytologia 78: 134-150. ------, and T. Demeke. 1993. Systematic relationships in Juniperus based on random amplified polymorphic DNAs (RAPDs). Taxon 42: 553-571. Adams, W.P. 1957. A revision of the genus Ascyrum (Hypericaceae). Rhodora 59: 73-95. ------. 1962. Studies in the Guttiferae. I. A synopsis of Hypericum section Myriandra. Contr. Gray Herbarium Harv. 182: 1-51. ------, and N.K.B. Robson. 1961. A re-evaluation of the generic status of Ascyrum and Crookea (Guttiferae). Rhodora 63: 10-16. Adams, W.P. 1973. Clusiaceae of the southeastern United States. J. Elisha Mitchell Sci. Soc. 89: 62-71. Adler, L. 1999. Polygonum perfoliatum (mile-a-minute weed). Chinquapin 7: 4. Aedo, C., J.J. Aldasoro, and C. Navarro. 1998. Taxonomic revision of Geranium sections Batrachioidea and Divaricata (Geraniaceae). Ann. Missouri Bot. Gard. 85: 594-630. Affolter, J.M. 1985. A monograph of the genus Lilaeopsis (Umbelliferae). Systematic Bot. Monographs 6. Ahles, H.E., and A.E. -
Contributions to the Solution of Phylogenetic Problem in Fabales
Research Article Bartın University International Journal of Natural and Applied Sciences Araştırma Makalesi JONAS, 2(2): 195-206 e-ISSN: 2667-5048 31 Aralık/December, 2019 CONTRIBUTIONS TO THE SOLUTION OF PHYLOGENETIC PROBLEM IN FABALES Deniz Aygören Uluer1*, Rahma Alshamrani 2 1 Ahi Evran University, Cicekdagi Vocational College, Department of Plant and Animal Production, 40700 Cicekdagi, KIRŞEHIR 2 King Abdulaziz University, Department of Biological Sciences, 21589, JEDDAH Abstract Fabales is a cosmopolitan angiosperm order which consists of four families, Leguminosae (Fabaceae), Polygalaceae, Surianaceae and Quillajaceae. The monophyly of the order is supported strongly by several studies, although interfamilial relationships are still poorly resolved and vary between studies; a situation common in higher level phylogenetic studies of ancient, rapid radiations. In this study, we carried out simulation analyses with previously published matK and rbcL regions. The results of our simulation analyses have shown that Fabales phylogeny can be solved and the 5,000 bp fast-evolving data type may be sufficient to resolve the Fabales phylogeny question. In our simulation analyses, while support increased as the sequence length did (up until a certain point), resolution showed mixed results. Interestingly, the accuracy of the phylogenetic trees did not improve with the increase in sequence length. Therefore, this study sounds a note of caution, with respect to interpreting the results of the “more data” approach, because the results have shown that large datasets can easily support an arbitrary root of Fabales. Keywords: Data type, Fabales, phylogeny, sequence length, simulation. 1. Introduction Fabales Bromhead is a cosmopolitan angiosperm order which consists of four families, Leguminosae (Fabaceae) Juss., Polygalaceae Hoffmanns. -
Flora Mediterranea 26
FLORA MEDITERRANEA 26 Published under the auspices of OPTIMA by the Herbarium Mediterraneum Panormitanum Palermo – 2016 FLORA MEDITERRANEA Edited on behalf of the International Foundation pro Herbario Mediterraneo by Francesco M. Raimondo, Werner Greuter & Gianniantonio Domina Editorial board G. Domina (Palermo), F. Garbari (Pisa), W. Greuter (Berlin), S. L. Jury (Reading), G. Kamari (Patras), P. Mazzola (Palermo), S. Pignatti (Roma), F. M. Raimondo (Palermo), C. Salmeri (Palermo), B. Valdés (Sevilla), G. Venturella (Palermo). Advisory Committee P. V. Arrigoni (Firenze) P. Küpfer (Neuchatel) H. M. Burdet (Genève) J. Mathez (Montpellier) A. Carapezza (Palermo) G. Moggi (Firenze) C. D. K. Cook (Zurich) E. Nardi (Firenze) R. Courtecuisse (Lille) P. L. Nimis (Trieste) V. Demoulin (Liège) D. Phitos (Patras) F. Ehrendorfer (Wien) L. Poldini (Trieste) M. Erben (Munchen) R. M. Ros Espín (Murcia) G. Giaccone (Catania) A. Strid (Copenhagen) V. H. Heywood (Reading) B. Zimmer (Berlin) Editorial Office Editorial assistance: A. M. Mannino Editorial secretariat: V. Spadaro & P. Campisi Layout & Tecnical editing: E. Di Gristina & F. La Sorte Design: V. Magro & L. C. Raimondo Redazione di "Flora Mediterranea" Herbarium Mediterraneum Panormitanum, Università di Palermo Via Lincoln, 2 I-90133 Palermo, Italy [email protected] Printed by Luxograph s.r.l., Piazza Bartolomeo da Messina, 2/E - Palermo Registration at Tribunale di Palermo, no. 27 of 12 July 1991 ISSN: 1120-4052 printed, 2240-4538 online DOI: 10.7320/FlMedit26.001 Copyright © by International Foundation pro Herbario Mediterraneo, Palermo Contents V. Hugonnot & L. Chavoutier: A modern record of one of the rarest European mosses, Ptychomitrium incurvum (Ptychomitriaceae), in Eastern Pyrenees, France . 5 P. Chène, M.