A Brief History of the North Central Regional Plant Introduction Station and a List of Genera Maintained
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Sigesbeckia Orientalis Click on Images to Enlarge
Species information Abo ut Reso urces Hom e A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Sigesbeckia orientalis Click on images to enlarge Family Asteraceae Scientific Name Sigesbeckia orientalis L. Linnaeus, C. von (1753) Species Plantarum 2: 900. Type: Habitat in China, Media ad pagos. Common name Flower head. Copyright Barry Jago Indian Weed; Farmer's Lice Weed * Stem Usually flowers and fruits as a shrub about 1 m tall but also flowers when smaller. Leaves Habit, leaves and flowers. Copyright CSIRO Leaves variable, leaf blades up to 6 x 3-3.5 cm, lower surface clothed in numerous small yellow glands. Lateral veins forming loops well inside the blade margin. Both the upper and lower surfaces of the leaf blade hairy. Twigs marked by scars resembling stipular scars. Stems hollow, pith absent. Flowers Flowers sessile in heads, about 15 flowers per head. Each head of flowers usually contains some female flowers, each consisting of a +/- 3-lobed perianth, and some hermaphrodite flowers with a 5-lobed perianth tube enclosing five anthers fused into a tube. Each head subtended by an involucre of about five green spathulate bracts which are clothed in sticky glands. Outer bracts about 5-10 x 0.5 mm. Corolla orange or yellow in the upper half but green in the lower half. Ovary glabrous. Fruit Scale bar 10mm. Copyright CSIRO Disk achenes 4-angular, about 2-5 mm long. Ray achenes clasped by persistent glandular hairy bracts. -
Chromosome Numbers in Compositae, XII: Heliantheae
SMITHSONIAN CONTRIBUTIONS TO BOTANY 0 NCTMBER 52 Chromosome Numbers in Compositae, XII: Heliantheae Harold Robinson, A. Michael Powell, Robert M. King, andJames F. Weedin SMITHSONIAN INSTITUTION PRESS City of Washington 1981 ABSTRACT Robinson, Harold, A. Michael Powell, Robert M. King, and James F. Weedin. Chromosome Numbers in Compositae, XII: Heliantheae. Smithsonian Contri- butions to Botany, number 52, 28 pages, 3 tables, 1981.-Chromosome reports are provided for 145 populations, including first reports for 33 species and three genera, Garcilassa, Riencourtia, and Helianthopsis. Chromosome numbers are arranged according to Robinson’s recently broadened concept of the Heliantheae, with citations for 212 of the ca. 265 genera and 32 of the 35 subtribes. Diverse elements, including the Ambrosieae, typical Heliantheae, most Helenieae, the Tegeteae, and genera such as Arnica from the Senecioneae, are seen to share a specialized cytological history involving polyploid ancestry. The authors disagree with one another regarding the point at which such polyploidy occurred and on whether subtribes lacking higher numbers, such as the Galinsoginae, share the polyploid ancestry. Numerous examples of aneuploid decrease, secondary polyploidy, and some secondary aneuploid decreases are cited. The Marshalliinae are considered remote from other subtribes and close to the Inuleae. Evidence from related tribes favors an ultimate base of X = 10 for the Heliantheae and at least the subfamily As teroideae. OFFICIALPUBLICATION DATE is handstamped in a limited number of initial copies and is recorded in the Institution’s annual report, Smithsonian Year. SERIESCOVER DESIGN: Leaf clearing from the katsura tree Cercidiphyllumjaponicum Siebold and Zuccarini. Library of Congress Cataloging in Publication Data Main entry under title: Chromosome numbers in Compositae, XII. -
Genetic Diversity, Phylogenetics and Molecular Systematics of Guizotia Cass
Genetic Diversity, Phylogenetics and Molecular Systematics of Guizotia Cass. (Asteraceae) Mulatu Geleta Faculty of Landscape Planning, Horticulture and Agricultural Science Department of Plant Protection Biology Alnarp Doctoral thesis Swedish University of Agricultural Sciences Alnarp 2007 Acta Universitatis Agriculturae Sueciae 2007:27 ISSN 1652-6880 ISBN 978-91-576-7326-8 © 2007 Mulatu Geleta, Alnarp Tryck: SLU Service/Repro, Alnarp 2007 Abstract Geleta, M. 2007. Genetic diversity, phylogenetics and molecular systematics of Guizotia Cass. (Asteraceae). Doctoral dissertation. ISSN 1652-6880, ISBN 978-91-576-7326-8. The genus Guizotia belongs to the tribe Heliantheae in the family Asteraceae. It has been placed under different subtribes. The genus has its center of origin, distribution and genetic diversity in Ethiopia, where G. abyssinica (niger) has been domesticated. Amplified Fragment Length Polymorphism (AFLP), Random Amplified Polymorphic DNA (RAPD) and DNA sequencing were applied to study the genetic diversity, phylogenetics, and molecular systematics of this genus. A large number of niger populations, representing all regions in Ethiopia where this crop is grown, was investigated using AFLP and RAPD molecular marker techniques. The extent of genetic variation in niger is distributed throughout its growing regions, regardless of the extent and altitude of cultivation. Despite the fact that most of the variation was within populations, significant population differentiation was obtained (AMOVA; P < 0.001) in all guizotias. It is concluded that both G. abyssinica and its wild and/or weedy relatives have wide genetic bases that need to be conserved and utilized for the improvement of G. abyssinica. Further collection of niger germplasm and exploration and conservation of highly localized guizotias are recommended. -
1. XANTHOCERAS Bunge, Enum. Pl. China Bor. 11. 1833
Flora of China 12: 6–7. 2007. 1. XANTHOCERAS Bunge, Enum. Pl. China Bor. 11. 1833. 文冠果属 wen guan guo shu Shrubs or trees. Leaves imparipinnate; leaflets serrate. Bracts ovate, large; flowers polygamous, male flowers and bisexual flowers on same plant but not in same inflorescence, actinomorphic. Sepals 5, oblong, imbricate. Petals 5, broadly obovate, shortly clawed, scale absent. Disk 5-lobed, lobes alternate to petals, apex with a hornlike appendage abaxially. Stamens 8, not exserted; anthers ellipsoid, apex of connectives and base of cells with 1 globose gland. Ovary ellipsoid, 3-loculed; ovules 7 or 8 per locule, in 2 lines; style terminal, erect; stigma papillate. Capsules subglobose or broadly ellipsoid, 3-ridged, loculicidal into 3 schizocarps, 3- loculed; pericarp thick, rigid, containing fiber bundles. Seeds several per locule, compressed-globose, pericarp thickly leathery, arillode absent; hilum semilunar, large; embryo arched, cotyledons one large and one small. 2n = 30. One species: N and NE China, Korea. There is some support based primarily on DNA sequence data to place Xanthoceras as sister to all other members of Sapindaceae s.l. including Aceraceae and Hippocastanaceae (see Harrington et al., Syst. Bot. 30: 366. 2005). Xanthoceras enkianthiflorum H. Léveillé (Repert. Spec. Nov. Regni Veg. 12: 534. 1913, “enkianthiflora”), described from Guizhou, is a syno- nym of Staphylea holocarpa Hemsley in the Staphyleaceae (see Fl. China 11). 1. Xanthoceras sorbifolium Bunge, Enum. Pl. China Bor. 11. sharply serrate; terminal leaflet usually deeply 3-lobed. Inflo- 1833 [“sorbifolia”]. rescences terminal, male ones axillary, erect, 12–20 cm; pedun- cle short, often with rudimentary scales at base. -
'Yan Xia': a Novel Cultivar of Xanthoceras Sorbifolium Bunge
HORTSCIENCE 56(4):511–512. 2020. https://doi.org/10.21273/HORTSCI15481-20 surviving grafted plantlets were collected, and second-generation grafted plantlets were cultivated. A 90% survival rate was attained ‘Yan Xia’: A Novel Cultivar of in consecutive grafting experiments. All grafted plantlets flowered in 2016. ‘Yan Xanthoceras sorbifolium Bunge with Xia’ displayed the same traits as the maternal parent, indicating the traits are genetically Ornamental Value stable (Ao, 2016a). Yuxin Chen Plant Characteristics Key Laboratory for Silviculture and Conservation, Ministry of Education, Beijing Forestry University, No. 35 Qinghua East Road, Haidian District, ‘Yan Xia’ is expected to be propagated in North China. It can reach a mature height of 2 Beijing 100083, China; and Beijing Laboratory of Urban and Rural to 7 m. It has racemose inflorescences, and Ecological Environment, No. 35 Qinghua East Road, Haidian District, the flowers bloom before or at the same time Beijing 100083, China as leaf sprouting (Fig. 1A). Normally, each flower has 20 petals. The petals are twisted Zishuo Zhang, Kexin Wang, Lijin Ou, and Yan Ao and curled, and are of various sizes. The Key Laboratory for Silviculture and Conservation, Ministry of Education, petals near the outer edges of flowers are Beijing Forestry University, No. 35 Qinghua East Road, Haidian District, wide and large; those near the center are Beijing 100083, China narrow and small. The pistil, stamens, and golden hornlike appendages mutate into Additional index words. cultivation technology, economic value, plant breeding, urban petals, making ‘Yan Xia’ a nonfruiting cul- afforestation, yellow-horn tivar (Fig. 2A) (Ao, 2016b). The sacs on the inner small petals are derived from yellow anthers filled with pollen. -
New Flavonoids from Seed Skin of Xanthoceras Sorbifolia
Journal of Medicinal Plants Research Vol. 5(6), pp. 1034-1036, 18 March, 2011 Available online at http://www.academicjournals.org/JMPR ISSN 1996-0875 ©2011 Academic Journals Short Communication New flavonoids from seed skin of Xanthoceras sorbifolia Rashmi 1* and Akito Nagatsu 2 1Chemistry Division, Forest Research Institute, Dehradun-248006, India. 2College of Pharmacy, Kinjo Gakuin University, Oomori, Moriyama, Nagoya 463-8521, Japan. Accepted 12 January, 2011 From ethyl acetate extract of seed skin of Xanthoceras sorbifolia, one compound with other known compounds was isolated by column chromatography on acetone: water: acetic acid solvent system. Structural elucidation of these compounds was carried out on the basis of Nuclear Magnetic Resonance (NMR) studies, namely 1HNMR, 13 CNMR, HMBC, HMQC and other 2D spectroscopy. Key words: Xanthoceras sorbifolia, Sapindaceae, seed skin, flavonoids, epigallocatechin. INTRODUCTION Xanthoceras sorbifolia also named as Xanthoceras theasapogenolB, 3β,23-di hydroxy-lup-20(29)en-28- sorbifolium belongs to the family Sapindaceae. It is oicacid-23-caffeate have been isolated from fruits and commonly known as yellowhorn and a member of the husks of X. sorbifolia (Li et al., 2005; Li et al., 2006; Chan soapberry family and hence closely related to maples, et al., 2008; Li et al., 2006). horse-chestnuts and lychee (Chen et al., 1985). It is a Saponins are widely present in X. sorbifolia and have kind of woody oil bearing shrub and originated primarily been reported to possess cytotoxic activity. Its wood, at Loess plateau in North of China and Inner Mangolia bark and fruits are used to treat rheumatism, gout and with characters of drought enduring, cold resistant and enuresis of children as a folk medicine (Li et al., 2007). -
Leonuri Cardiacae Herba
16 September 2010 EMA/HMPC/127429/2010 Committee on Herbal Medicinal Products (HMPC) List of references supporting the assessment of Leonurus cardiaca L., herba Final The Agency acknowledges that copies of the underlying works used to produce this monograph were provided for research only with exclusion of any commercial purpose. Abascal K, Yarnell E (2004) Nervine herbs for treating anxiety. Alternative & Complementary Therapies (England); 10:309-315 Abebe W (2002) Herbal medication: Potential for adverse interactions with analgesic drugs. Journal of Clinical Pharmacy and Therapeutics; 27:391-401 Agnihotri VK, ElSohly HN, Smillie TJ, Khan IA, Walker LA (2008) New Labdane Diterpenes from Leonurus cardiaca. Planta Med; 74:1288-1290 Ahmed F, Islam MA, Rahman MM (2006) Antibacterial activity of Leonurus sibiricus aerial parts. Fitoterapia; 77:316-317 Ahmed F, Islam MA, Choudhuri MSK (2005) Central nervous system depressant activity of Leonurus sibiricus. Nigerian Journal of Natural Products and Medicine; 9:35-37 Aizetmüller K, Tsevegüren N (1998) Phlomic acid in Lamioidae seed oils. Lamiales Newsletter; 6:13-16 Ali MS, Ibrahim SA, Jalil S, Choudhary MI (2007) Ursolic acid: A potent inhibitor of superoxides produced in the cellular system. Phytotherapy Res; 21:558-561 Almeida LFR, Delachiave MEA, Marques MOM (2005) Composição do óleo essencial de rubim (Leonurus sibiricus L. - Lamiaceae). [Composition of the essential oil of rubim (Leonurus sibiricus L. - Lamiaceae).] Revista Brasileira de Plantas Medicinais; 8:35-38 American Botanical Council (2008) Herbs for potential adjunct treatment of thyroid disease. A review of botanical preparations for hypo- and hyperthyroidism, thyroid nodules, and thyroid cancer. HerbalGram; 79:52-65 7 Westferry Circus ● Canary Wharf ● London E14 4HB ● United Kingdom Telephone +44 (0)20 7418 8400 Facsimile +44 (0)20 7523 7051 E-mail [email protected] Website www.ema.europa.eu An agency of the European Union © European Medicines Agency, 2010. -
Species Association in Xanthoceras Sorbifolium Bunge Communities and Selection for Agroforestry Establishment
Agroforest Syst https://doi.org/10.1007/s10457-018-0265-z Species association in Xanthoceras sorbifolium Bunge communities and selection for agroforestry establishment Qing Wang . Renbin Zhu . Jimin Cheng . Zhixiong Deng . Wenbin Guan . Yousry A. El-Kassaby Received: 24 August 2017 / Accepted: 15 June 2018 Ó The Author(s) 2018 Abstract We embraced the ‘‘learning from nature scaling ordination to assess community structure and and back to nature’’ paradigm to develop viable composition, and the climatic variables that most agroforestry scenarios through studying species asso- likely influenced existing species distributions. Next, ciation in 12 wild yellowhorn (Xanthoceras sorb- pairwise and multiple species associations were eval- ifolium: a Chinese endemic oil woody plants) uated using several multiple species association communities. We identified 18 species combinations indices (e.g., v2, Jaccard, Ochiai, Dice). Generally, for their suitability as agroforestry mixes where all species association indices were in agreement and positive associations were detected and thus economic were helpful in identifying several high valued benefits are anticipated. In each wild yellowhorn medicinal species that showed positive and significant community, we use nonmetric multidimensional associations with yellowhorn. Finally, we proposed several agroforestry species mixes suitable for yellowhorn. Qing Wang and Renbin Zhu have contributed equally to this work. Keywords Xanthoceras sorbifolium Á Species Electronic supplementary material The online version of association and selection Á Agroforestry mixes Á this article (https://doi.org/10.1007/s10457-018-0265-z) con- Nonmetric multidimensional scaling ordination tains supplementary material, which is available to authorized users. (NMDS) Q. Wang Á Z. Deng Á W. Guan (&) R. Zhu School of Nature Conservation, Beijing Forestry Xishuangbanna Tropical Botanical Garden, Chinese University, Beijing 100083, People’s Republic of China Academy of Sciences, Menglun 666303, Yunnan, e-mail: [email protected] People’s Republic of China Q. -
Supplement to the Systematics of the Heliantheae (Compositae)
Boletín de la Sociedad Argentina de Botánica Volumen XIX, N? 1-2 (Julio 1980), págs. 25-32 SUPPLEMENT TO THE SYSTEMATICS OF THE HELIANTHEAE (COMPOSITAE) Por TOD F. STUESSY2 Since the completion of a revised subtribal classification of the tribe Heliantheae (Stuessy, in press) for the Reading Symposium on the Compositae in July of 1975, a number of new papers have been published on the systematics of the tribe. This new informa¬ tions falls into four general categories: (1) speculations on relation¬ ships among the newly recognized subtribes; (2) addition of a new subtribe; (3) additions of new genera; and (4) new generic transfers. The purpose of this paper is to review these new developments and comment on their significance for the systematics of the Heliantheae. RELATIONSHIPS AMONG THE NEWLY RECOGNIZED SUBTRIBES An important new overview of relationships among the sub¬ tribes of the Heliantheae has been provided by Baagoe (1977) by use of ligule microcharacters. This contribution is especially valuable, because the manuscript on the Heliantheae for the Reading Sympo¬ sium (Stuessy, in press) was available to Dr. Baagoe during her study, and she was able to relate the new data to the subtribal clas¬ sification of the tribe. Many specific comments on relationships are contained in her paper, but this review will focus only on some of the broader implications. Before these are examined, however, a few cautions need to be raised. 1 It is a pleasure to dedicate this paper to Dr. Angel L. Cabrera, one of the outstanding synantherologists of the world, and the unqualified authority on South American Compositae. -
Sigesbeckia Orientalis L
Australian Tropical Rainforest Plants - Online edition Sigesbeckia orientalis L. Family: Asteraceae Linnaeus, C. von (1753) Species Plantarum 2: 900. Type: Habitat in China, Media ad pagos. Common name: Indian Weed; Farmer's Lice Stem Usually flowers and fruits as a shrub about 1 m tall but also flowers when smaller. Leaves Leaves variable, leaf blades up to 6 x 3-3.5 cm, lower surface clothed in numerous small yellow glands. Lateral veins forming loops well inside the blade margin. Both the upper and lower surfaces of the leaf blade hairy. Twigs marked by scars resembling stipular scars. Stems hollow, pith absent. Flowers Flowers sessile in heads, about 15 flowers per head. Each head of flowers usually contains some female flowers, each consisting of a +/- 3-lobed perianth, and some hermaphrodite flowers with a 5- lobed perianth tube enclosing five anthers fused into a tube. Each head subtended by an involucre Flower head. © Barry Jago of about five green spathulate bracts which are clothed in sticky glands. Outer bracts about 5-10 x 0.5 mm. Corolla orange or yellow in the upper half but green in the lower half. Ovary glabrous. Fruit Disk achenes 4-angular, about 2-5 mm long. Ray achenes clasped by persistent glandular hairy bracts. Seedlings Hypocotyl clothed in short erect hairs just visible with a lens. Stem above the cotyledons clothed in much longer erect white hairs. Cotyledons +/- orbicular, about 6-7 x 5-6 mm. First pair of leaves with toothed margins. At the tenth leaf stage: stem, terminal bud and both the upper and lower leaf blade surfaces clothed in white somewhat scabrous hairs. -
The Naturalized Vascular Plants of Western Australia 1
12 Plant Protection Quarterly Vol.19(1) 2004 Distribution in IBRA Regions Western Australia is divided into 26 The naturalized vascular plants of Western Australia natural regions (Figure 1) that are used for 1: Checklist, environmental weeds and distribution in bioregional planning. Weeds are unevenly distributed in these regions, generally IBRA regions those with the greatest amount of land disturbance and population have the high- Greg Keighery and Vanda Longman, Department of Conservation and Land est number of weeds (Table 4). For exam- Management, WA Wildlife Research Centre, PO Box 51, Wanneroo, Western ple in the tropical Kimberley, VB, which Australia 6946, Australia. contains the Ord irrigation area, the major cropping area, has the greatest number of weeds. However, the ‘weediest regions’ are the Swan Coastal Plain (801) and the Abstract naturalized, but are no longer considered adjacent Jarrah Forest (705) which contain There are 1233 naturalized vascular plant naturalized and those taxa recorded as the capital Perth, several other large towns taxa recorded for Western Australia, com- garden escapes. and most of the intensive horticulture of posed of 12 Ferns, 15 Gymnosperms, 345 A second paper will rank the impor- the State. Monocotyledons and 861 Dicotyledons. tance of environmental weeds in each Most of the desert has low numbers of Of these, 677 taxa (55%) are environmen- IBRA region. weeds, ranging from five recorded for the tal weeds, recorded from natural bush- Gibson Desert to 135 for the Carnarvon land areas. Another 94 taxa are listed as Results (containing the horticultural centre of semi-naturalized garden escapes. Most Total naturalized flora Carnarvon). -
Plastid and Nuclear DNA Markers.Pdf
Molecular Phylogenetics and Evolution 51 (2009) 238–258 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Plastid and nuclear DNA markers reveal intricate relationships at subfamilial and tribal levels in the soapberry family (Sapindaceae) Sven Buerki a,*, Félix Forest b, Pedro Acevedo-Rodríguez c, Martin W. Callmander d,e, Johan A.A. Nylander f, Mark Harrington g, Isabel Sanmartín h, Philippe Küpfer a, Nadir Alvarez a a Institute of Biology, University of Neuchâtel, Rue Emile-Argand 11, CH-2009 Neuchâtel, Switzerland b Molecular Systematics Section, Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3DS, United Kingdom c Department of Botany, Smithsonian Institution, National Museum of Natural History, NHB-166, Washington, DC 20560, USA d Missouri Botanical Garden, PO Box 299, 63166-0299, St. Louis, MO, USA e Conservatoire et Jardin botaniques de la ville de Genève, ch. de l’Impératrice 1, CH-1292 Chambésy, Switzerland f Department of Botany, Stockholm University, SE-10691, Stockholm, Sweden g School of Marine and Tropical Biology, James Cook University, PO Box 6811, Cairns, Qld 4870, Australia h Department of Biodiversity and Conservation, Real Jardin Botanico – CSIC, Plaza de Murillo 2, 28014 Madrid, Spain article info abstract Article history: The economically important soapberry family (Sapindaceae) comprises about 1900 species mainly found Received 21 May 2008 in the tropical regions of the world, with only a few genera being restricted to temperate areas. The inf- Revised 27 November 2008 rafamilial classification of the Sapindaceae and its relationships to the closely related Aceraceae and Hip- Accepted 23 January 2009 pocastanaceae – which have now been included in an expanded definition of Sapindaceae (i.e., subfamily Available online 30 January 2009 Hippocastanoideae) – have been debated for decades.