Three New Crûg Farm Introductions
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Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE
Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE LILIACEAE de Jussieu 1789 (Lily Family) (also see AGAVACEAE, ALLIACEAE, ALSTROEMERIACEAE, AMARYLLIDACEAE, ASPARAGACEAE, COLCHICACEAE, HEMEROCALLIDACEAE, HOSTACEAE, HYACINTHACEAE, HYPOXIDACEAE, MELANTHIACEAE, NARTHECIACEAE, RUSCACEAE, SMILACACEAE, THEMIDACEAE, TOFIELDIACEAE) As here interpreted narrowly, the Liliaceae constitutes about 11 genera and 550 species, of the Northern Hemisphere. There has been much recent investigation and re-interpretation of evidence regarding the upper-level taxonomy of the Liliales, with strong suggestions that the broad Liliaceae recognized by Cronquist (1981) is artificial and polyphyletic. Cronquist (1993) himself concurs, at least to a degree: "we still await a comprehensive reorganization of the lilies into several families more comparable to other recognized families of angiosperms." Dahlgren & Clifford (1982) and Dahlgren, Clifford, & Yeo (1985) synthesized an early phase in the modern revolution of monocot taxonomy. Since then, additional research, especially molecular (Duvall et al. 1993, Chase et al. 1993, Bogler & Simpson 1995, and many others), has strongly validated the general lines (and many details) of Dahlgren's arrangement. The most recent synthesis (Kubitzki 1998a) is followed as the basis for familial and generic taxonomy of the lilies and their relatives (see summary below). References: Angiosperm Phylogeny Group (1998, 2003); Tamura in Kubitzki (1998a). Our “liliaceous” genera (members of orders placed in the Lilianae) are therefore divided as shown below, largely following Kubitzki (1998a) and some more recent molecular analyses. ALISMATALES TOFIELDIACEAE: Pleea, Tofieldia. LILIALES ALSTROEMERIACEAE: Alstroemeria COLCHICACEAE: Colchicum, Uvularia. LILIACEAE: Clintonia, Erythronium, Lilium, Medeola, Prosartes, Streptopus, Tricyrtis, Tulipa. MELANTHIACEAE: Amianthium, Anticlea, Chamaelirium, Helonias, Melanthium, Schoenocaulon, Stenanthium, Veratrum, Toxicoscordion, Trillium, Xerophyllum, Zigadenus. -
Genetic Diversity of the Traditional Chinese Medicinal Plant Ypsilandra Thibetica (Melanthiaceae): Applications for Conservation
Biochemical Systematics and Ecology 39 (2011) 425–433 Contents lists available at ScienceDirect Biochemical Systematics and Ecology journal homepage: www.elsevier.com/locate/biochemsyseco Genetic diversity of the traditional Chinese medicinal plant Ypsilandra thibetica (Melanthiaceae): Applications for conservation Hong-Tao Li a,b, Hong Wang a, Jun-Bo Yang a,b, De-Zhu Li a,b,* a Key Laboratory of Biodiversity and Biogeography, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming Yunnan 650204, China b The Germplasm Bank of Wild Species in Southwest China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan 650204, China article info abstract Article history: Twelve microsatellite markers were developed to determine the genetic diversity and Received 31 December 2010 genetic structure of Ypsilandra thibetica, represented by a total of 90 individuals from six Accepted 3 June 2011 natural populations. All twelve microsatellite loci were polymorphic, and the results Available online 28 June 2011 indicated that a high genetic diversity was present within populations (mean RS ¼ 4.996; mean HE ¼ 0.615), with high levels of genetic structure (mean FST ¼ 0.165; mean Keywords: FIS ¼ 0.692) among populations. This pattern is likely attributable to consanguineous Conservation mating, and this hypothesis is supported by a low relatedness coefficient. Our study Genetic diversity fl Gene flow suggested that environment factors might restrict gene ow among populations. In Microsatellite markers addition, physical distances between populations were not related to genetic distances, Ypsilandra thibetica implying that ancestral populations might have been distributed over a wider area. These results suggest that Y. thibetica should be a high priority for conservation managers. -
J. Jpn. Bot. 73
植物研究雑誌 J. J. Jpn. Bo t. 73: 73: 102-115 (1 998) Phylogenetic Phylogenetic and Taxonomic Studies onHelonias ,Ypsilandra andHeloniopsis 111. 111. Taxonomic Revision Noriyuki Noriyuki TANAKA Department Department of Education ,School of Liberal Arts ,Teikyo University 359 359 Otsuka ,Hachioji-shi ,Tokyo ,192-0395 JAPAN (Received (Received on April 2 ,1997) The three genera ,Helonias ,浄silandra and Heloniopsis have not sufficient differ- ences ences to be distinguished from each other in generic rank. Accordingly the three genera were were unified into one genus. Heloniopsis and Ypsilandra were reduced to Helonias. The following following taxonomic reductions were also made in this paper; i.e. , both Y. cav αleriei and Y. Y. kansuensis were reduced to Helonias thibetic α; both Heloniopsis arisanensis and eloniopsis H eloniopsis taiwanensis to Helonias umbellata; Y. yunnanensis var. himalaica to Helonias yunnanensis; yunnanensis; Sugerokia nipponica ,Heloniopsis japonica v紅 .flavida , H. japonica v紅. albiflora albiflora and H. japonica var. tessellata to Helonias breviscapa. Fl oral colour variants were were not distinguished as distinct taxa. As a result , a total of nine species were recognized in in the emended Heloni ω. Eight new names were produced as a consequence of the transference transference of both ゆsilandra and Heloniopsis to Helonias. (Continued (Continued from 1. Jpn. Bo t. 72: 329-336 , 1997) According to my previous studies (Tanaka H. kawanoi , the basal part of the inner fila- 1997a ,1997c-e) ,Helonias and Ypsilandra ments is located very close to that of the ovary , differ differ mainly in the following characters; i.e. , and this state does not differ so markedly from themo ゅhology of seeds , the number of ovules that in Ypsilandra in which the two floral per per loculus of an ov 紅 y, the number of flowers organs are adnate to each other only very per per scape ,and the presence or absence of a shortly at their bases. -
A Synopsis of Melanthiaceae (Liliales) with Focus on Character Evolution in Tribe Melanthieae Wendy B
Aliso: A Journal of Systematic and Evolutionary Botany Volume 22 | Issue 1 Article 44 2006 A Synopsis of Melanthiaceae (Liliales) with Focus on Character Evolution in Tribe Melanthieae Wendy B. Zomlefer University of Georgia Walter S. Judd University of Florida W. Mark Whitten University of Florida Norris H. Williams University of Florida Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons Recommended Citation Zomlefer, Wendy B.; Judd, Walter S.; Whitten, W. Mark; and Williams, Norris H. (2006) "A Synopsis of Melanthiaceae (Liliales) with Focus on Character Evolution in Tribe Melanthieae," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 22: Iss. 1, Article 44. Available at: http://scholarship.claremont.edu/aliso/vol22/iss1/44 Aliso 22, pp. 566-578 © 2006, Rancho Santa Ana Botanic Garden A SYNOPSIS OF MELANTHIACEAE (LILIALES) WITH FOCUS ON CHARACTER EVOLUTION IN TRIBE MELANTHIEAE WENDY B. ZOMLEFER, 1.4 WALTERS. JUDD,2 W. MARK WHITTEN, 3 AND NORRIS H. WILLIAMS3 1Department of Plant Biology, University of Georgia, 2502 Miller Plant Sciences, Athens, Georgia 30602-7271, USA; 2Department of Botany, University of Florida, PO Box 118526, Gainesville, Florida 32611-8526, USA ([email protected]); 3Department of Natural Sciences, Florida Museum of Natural History, University of Florida, PO Box 117800, Gainesville, Florida 32611-7800, USA ([email protected]), ([email protected]) 4 Corresponding author ([email protected]) ABSTRACT Melanthiaceae s.l. comprises five tribes: Chionographideae, Heloniadeae, Melanthieae, Parideae, and Xerophylleae--each defined by distinctive autapomorphies. The most morphologically diverse tribe Melanthieae, now with seven genera, had not been subject to rigorous phylogenetic character study prior to the current series of investigations that also include an overview of the family. -
Medicinal Plant Conservation
MEDICINAL Medicinal Plant PLANT SPECIALIST Conservation GROUP Volume 15 Newsletter of the Medicinal Plant Specialist Group of the IUCN Species Survival Commission Chaired by Danna J. Leaman Chair’s note .......................................................................................................................................... 2 Taxon file Conservation of the Palo Santo tree, Bulnesia sarmientoi Lorentz ex Griseb, in the South America Chaco Region - Tomás Waller, Mariano Barros, Juan Draque & Patricio Micucci ............................. 4 Manejo Integral de poblaciones silvestres y cultivo agroecológico de Hombre grande (Quassia amara) en el Caribe de Costa Rica, América Central - Rafael Ángel Ocampo Sánchez ....................... 9 Regional file Chilean medicinal plants - Gloria Montenegro & Sharon Rodríguez ................................................. 15 Focus on Medicinal Plants in Madagascar - Julie Le Bigot ................................................................. 25 Medicinal Plants utilisation and conservation in the Small Island States of the SW Indian Ocean with particular emphasis on Mauritius - Ameenah Gurib-Fakim ............................................................... 29 Conservation assessment and management planning of medicinal plants in Tanzania - R.L. Mahunnah, S. Augustino, J.N. Otieno & J. Elia...................................................................................................... 35 Community based conservation of ethno-medicinal plants by tribal people of Orissa state, -
Steroidal Saponin Ypsilandra Thibetica Induces Apoptosis in Colorectal Carcinoma Cells Through the Mitochondrion-Dependent Reactive Oxygen Species Pathway
INTERNATIONAL JOURNAL OF AGRICULTURE & BIOLOGY ISSN Print: 1560–8530; ISSN Online: 1814–9596 19F–018/2019/22–2–326–330 DOI: 10.17957/IJAB/15.1067 http://www.fspublishers.org Full Length Article Steroidal Saponin Ypsilandra thibetica Induces Apoptosis in Colorectal Carcinoma Cells through the Mitochondrion-Dependent Reactive Oxygen Species Pathway Zhendong Zhao, Li Xia*, Dandan Xu, Guohong Zhou, Huiqing Huang, Daiying Zhou, Jin Lin, Shaolin Li and Jia Liu School of Chinese Materia Medica, Guangdong Food and Drug Vocational College, Guangzhou 510520, P.R. China *For correspondence: [email protected] Abstract The whole plant of Ypsilandra thibetica Franch, a perennial herb, has the officinal functions in heat-clearing, detoxifying and relieving congeation. YB16, one of the steroidal saponin in Y. thibetic, exerts anticancer activity in prostate cancer and lung cancer. However, the bioactivity and underlying mechanisms of YB16 in colorectal carcinoma (CRC) are not understood. In the present study, by MTT, apoptosis, mitochondrial membrane potential levels and intercellular reactive oxygen species (ROS) assays, YB16 inhibited the proliferation of cells and induced apoptosis in CRC HCT116 and HCT8 cells. Meanwhile, YB16 provoked mitochondrial membrane potential depolarizing in a concentration-dependent manner. Further analysis showed that YB16 induced apoptosis via stimulating the production of intercellular ROS and the antioxidant NAC reversed the apoptosis in HCT116 and HCT8 after YB16 treatment. These datas demonstrated that YB16 induced -
Self-Guided Tour Late
Self-Guided Tour Late Welcome to the Rhododendron Species Botanical Garden (RSBG). This self-guided tour will take approximately 1-1.5 hours depending upon how long you spend ex- amining the plants. Please enjoy our 22 acre display of botanical splendor! Please keep in mind the following: Collecting seeds or any plant material is strictly prohibited. Smoking and pets are not allowed in the garden. Please remain on the paths. Picnicking is allowed only on the Con- servatory Terrace. 2525 South 336 St. Federal Way, WA 98063 253-838-4646 Microoft www.rhodygarden.org Open All Year, Tuesday to Sunday 10:00am to 4:00pm #1 Rhododendron strigillosum welcomes you to the gar- Now, go back to the main road and take a left. Walk From the stumpery, take the path to the pond den as you enter to the courtyard. This early flowering past the black bamboo on your left and a large garden (follow the sign). #15 Rhododendron la- species puts on a spectacular display every year. It has flowering Mahonia (#7) on your right. The bright nigerum is putting on a spectacular show this distinctive bristles on the midrib, petiole, and foliage. R. yellow flowers of this plant are a valuable food year and is from Tibet and India. Take a right strigillosum is native to Sichuan and NE Yunnan, China. source for over-wintering hummingbirds. turn to visit #16 Rhododendron ririei. The bell- shaped flowers are purplish in color with dark Turn left on the main road and continue to the path on nectar pouches and the lower surface of the the left. -
Genetic Diversity of Three European Veratrum Species Revealed by Amplified Fragment Length Polymorphism
Biodiv. Res. Conserv. 47: 1-8, 2017 BRC www.brc.amu.edu.pl DOI 10.1515/biorc-2017-0011 Submitted 13.06.2017, Accepted 30.09.2017 Genetic diversity of three European Veratrum species revealed by Amplified Fragment Length Polymorphism Magdalena Szeliga*, Joanna Ciura & Mirosław Tyrka Department of Biotechnology and Bioinformatics, Faculty of Chemistry, Rzeszow University of Technology, Powstańców Warszawy 6, 35-959 Rzeszów, Poland *corresponding author (e-mail: [email protected]) Abstract. Chemical and genetic characterization of Veratrum species deposited in European collections is important for genepool preservation and identification of populations with desired metabolic properties.Veratrum album, V. lobelianum and V. nigrum are native to Europe, and in Poland are ranked as rare or threatened. Genetic variation of European Veratrum species was characterized by Amplified Fragment Length Polymorphism (AFLP) markers. The accumulation of jervine as a represen- tative of steroidal alkaloids was measured in seeds. Distribution of 380 markers generated from eight primer combinations was useful for studying genetic relationships among and within species in the Veratrum genus and the most divergent populations were identified. Genetic variation between 12 populations ofVeratrum species supports the classification ofV. lobelianum as a subspecies of V. album. However, the results need further validation on extended material. A higher genetic diversity (22.3%) was observed between populations of V. nigrum as compared to V. album (14.5%). Contents of jervine allowed for discrimina- tion of the studied Veratrum species and can be used as a potential chemotaxonomic marker. The highest jervine levels were found in V. album. V. nigrum seeds had only trace amounts and no jervine was detected in seeds of V. -
A Synopsis of the Genus Chamaelirium (Melanthiaceae) with a New Infrageneric Classification Including Chionographis
Taiwania 62(2): 157‒167, 2017 DOI: 10.6165/tai.2017.62.157 A synopsis of the genus Chamaelirium (Melanthiaceae) with a new infrageneric classification including Chionographis Noriyuki TANAKA 98-11 Otsuka, Hachioji, Tokyo, 192-0352 Japan. Email: [email protected] (Manuscript received 4 October 2016; accepted 28 March 2017; online published 3 May 2017) ABSTRACT: Two closely allied genera Chamaelirium Willd. and Chionographis Maxim. distributed disjunctively in eastern North America and eastern Asia are taxonomically reexamined, and a new classification is presented. Chionographis is included in Chamaelirium, and the latter comprises two sections Chamaelirium and Chionographis (Maxim.) N. Tanaka (comb. nov.). The former is monotypic (C. luteum), while the latter is subdivided into two subsections Chionographis and Cathayana N. Tanaka (subsect. nov.). The former subsection comprises four species indigenous to Japan and Korea, and the latter has four species native to Vietnam, Laos and China. A total of 14 new combinations at or below the rank of species (eight at specific, three at subspecific, and three at varietal rank) are circumscribed. Sect. Stenotepalon F. Maek. is reduced to a synonym of sect. Chionographis. Chamaelirium luteum Miq. f. gracilis Miq. is also reduced to a synonym of Chamaelirium japonicum (Willd.) N. Tanaka. Chamaelirium (s.l.) and its infrageneric taxa (two sections and two subsections) are regarded respectively as monophyletic on the basis of morphological and phenological data. KEY WORDS: Chamaelirium, Chionographis, Diversity, Melanthiaceae, Monophyly, Phylogeny, Taxonomic revision. INTRODUCTION unequal tepals (vs. actinomorphic flowers with equal tepals) (Engler, 1887; Hara, 1968; Tanaka, 2003). Chamaelirium Willd. is a monotypic genus (C. -
Phylogenetic Classification of Seed Plants of Taiwan
Lin and Chung Bot Stud (2017) 58:52 DOI 10.1186/s40529-017-0206-6 ORIGINAL ARTICLE Open Access Phylogenetic Classifcation of Seed Plants of Taiwan Cheng‑Tao Lin1 and Kuo‑Fang Chung2* Abstract Background: Biological classifcation, the hierarchical arrangement of scientifc names of organisms, constitutes the core infrastructure of biological databases. For an efcient management of biological databases, adopting a stable and universal biological classifcation system is crucial. Currently in Taiwan Biodiversity Information Facility (TaiBIF; http://taibif.tw/), the national portal website that integrates Taiwan’s biodiversity information databases, angiosperms are arranged according to Cronquist’s System of Classifcation, which is not compatible with current trend of the Angiosperm Phylogeny Group (APG) classifcation. To consolidate the function and management of the database, TaiBIF is moving to adopt the APG IV classifcation and Christenhusz et al. (Phytotaxa 19:55–70, 2011)’s classifcation of gymnosperms, which we summarize as the Phylogenetic Classifcation of Seed Plants of Taiwan. Results: The Phylogenetic Classifcation of Seed Plants of Taiwan places gymnosperms in fve families [vs. eight families in the Flora of Taiwan (FOT)] and angiosperms in 210 families (vs. 193 families in FOT). Three FOT gymnosperm families are synonymized in current treatment. Of the 210 APG IV families, familial circumscriptions of 114 families are identical with FOT and 50 families are recircumscription of FOT, with 46 families newly added. Of the 29 FOT families not included in current classifcation, two families are excluded and 27 families are synonymized. Conclusions: The adoption of the Phylogenetic Classifcation of Seed Plants of Taiwan in TaiBIF will provide better service and efcient management of the nation’s biodiversity information databases. -
From Guangxi, China
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/317960938 Oreocharis crispata, a new species of Oreocharis (Gesneriaceae) from Guangxi, China Article in Phytotaxa · June 2017 DOI: 10.11646/phytotaxa.311.2.8 CITATIONS READS 2 46 6 authors, including: Wen-Hong Chen Yi-Gang Wei Chinese Academy of Sciences Guangxi Institute of Botany, CAS 31 PUBLICATIONS 104 CITATIONS 73 PUBLICATIONS 500 CITATIONS SEE PROFILE SEE PROFILE Fang Wen Yu M. Shui Guangxi Academy of Sciences Chinese Academy of Sciences 82 PUBLICATIONS 367 CITATIONS 61 PUBLICATIONS 281 CITATIONS SEE PROFILE SEE PROFILE Some of the authors of this publication are also working on these related projects: Karst vascular plant diversity View project Taxonomy of the species-rich genus Elatostema View project All content following this page was uploaded by Fang Wen on 11 May 2018. The user has requested enhancement of the downloaded file. Phytotaxa 311 (2): 195–199 ISSN 1179-3155 (print edition) http://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2017 Magnolia Press Article ISSN 1179-3163 (online edition) https://doi.org/10.11646/phytotaxa.311.2.8 Oreocharis crispata, a new species of Oreocharis (Gesneriaceae) from Guangxi, China RUN-ZHENG CHEN 1, 4, 5, WEN-HONG CHEN 1, 4, YI-GANG WEI 2, FANG WEN 2, XUN-LIN YU 3 & YU-MIN SHUI 1, 4, * 1 Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, the Chinese Academy of Sciences, Kunming 650201, China 2 Guangxi Institute of Botany, Guangxi Zhuang Autonomous Region and Chinese Academy of Sciences, Guilin 541006, China 3 College of Forestry, Central South University of Forestry and Technology, Changsha 410004, China 4 Karst Conservation Initiative of Yunnan, Kunming 650201, China 5 University of Chinese Academy of Sciences, Beijing 100049, China * Corresponding author: [email protected] Abstract Oreocharis crispata, a new species of Oreocharis (Gesneriaceae) from northeastern Guangxi, China, is described and illus- trated. -
6. YPSILANDRA Franchet, Nouv. Arch. Mus. Hist. Nat., Sér. 2, 10: 93
Flora of China 24: 86–87. 2000. 6. YPSILANDRA Franchet, Nouv. Arch. Mus. Hist. Nat., sér. 2, 10: 93. 1887. 丫蕊花属 ya rui hua shu Chen Xinqi (陈心启 Chen Sing-chi); Minoru N. Tamura Herbs perennial, with a short, thickened, slightly fleshy rhizome, glabrous. Leaves basal, rosulate, linear to lanceolate or oblan- ceolate, or spatulate, basally gradually narrowed to a petiole. Scape arising from axils of lateral leaves, erect, simple, with several to many scaly leaves. Inflorescence a terminal raceme, 2–30-flowered; bract absent. Flowers bisexual, usually nodding at anthesis, ascending in fruit, spreading funnelform. Tepals 6, free, with a nectary gland basally on adaxial side, persistent. Stamens 6, rather long, free from tepals, inner ones basally adnate to ovary, outer ones free; anthers usually reniform, basifixed, with confluent locules. Ovary superior, 3-lobed, 3-loculed; ovules many per locule. Style 1, very short to long; stigma capitate to 3-cleft. Fruit a capsule, trigonous, 3-lobed apically, loculicidal. Seeds numerous, narrowly fusiform, both ends caudate. Five species: Bhutan, China, Myanmar, Nepal; five species (three endemic) in China. 1a. Stamens and style not extending beyond tepals at anthesis; stigma shortly or deeply 3-lobed (lobes 0.3–0.8 mm). 2a. Stigma deeply 3-lobed (lobes ca. 0.8 mm); style 1–1.5 mm; tepals 4–5 mm, spatulate or oblanceolate to elliptic, shorter than capsule; flowers 5–17 per scape ....................................................................................... 4. Y. yunnanensis 2b. Stigma shortly to moderately 3-lobed (lobes 0.3–0.5 mm); style 2.5–6 mm; tepals 7–12 mm, linear to linear- lanceolate, longer than capsule; flowers 2–6 per scape .............................................................................................