LILIACEAE 百合科 Bai He Ke Chen Xinqi (陈心启 Chen Sing-Chi)1, Liang Songyun (梁松筠 Liang Song-Jun)2, Xu Jiemei (许介眉)3; Minoru N

Total Page:16

File Type:pdf, Size:1020Kb

LILIACEAE 百合科 Bai He Ke Chen Xinqi (陈心启 Chen Sing-Chi)1, Liang Songyun (梁松筠 Liang Song-Jun)2, Xu Jiemei (许介眉)3; Minoru N Flora of China 24: 73–263. 2000. LILIACEAE 百合科 bai he ke Chen Xinqi (陈心启 Chen Sing-chi)1, Liang Songyun (梁松筠 Liang Song-jun)2, Xu Jiemei (许介眉)3; Minoru N. Tamura4 Herbs perennial, with a rhizome, bulb, or corm, rarely shrubby or treelike. Leaves basal and/or cauline, alternate, opposite, or whorled, parallel or rarely reticulate veined. Inflorescence a raceme, panicle, spike, umbel, reduced panicle, or other, or flowers soli- tary. Flowers bisexual, rarely unisexual, actinomorphic, rarely zygomorphic; bracts present or absent; bracteoles present or absent. Perianth usually corollalike, 6-merous, rarely 4- or 8-merous, in 2 whorls; segments free (tepals) or united. Stamens 6, rarely 3, 4, or 8, inserted opposite perianth segments; filaments free or adnate to perianth, rarely connate into a corona; anthers usually 2-loculed, basifixed or dorsifixed and versatile, introrse, latrorse, or extrorse, dehiscing usually by vertical slits. Carpels usually connate for most or all of their length, rarely only at base; ovary superior, rarely semi-inferior, 3-loculed, rarely 2- or 4-loculed, with axile pla- centae, or rarely 1-loculed with a parietal placenta; ovules usually anatropous. Nectaries septal, perigonal, or absent. Fruit a capsule or berry. Seeds with abundant endosperm and small embryo. About 250 genera and 3500 species: worldwide, especially in temperate and subtropical regions; 57 genera (three endemic, two introduced) and 726 species (379 endemic, 11 introduced) in China. The circumscription adopted here for Liliaceae sensu lato follows FRPS and is not supported by current phylogenetic analysis of the group. However, the genus order has been adjusted to reflect the more recent classification of Kubitzki (Fam. Gen. Vasc. Pl. 3, 1998), who placed the genera in segregate families as follows: Alliaceae: Allium, Milula; Anemarrhenaceae: Anemarrhena; Anthericaceae: Chlorophytum, Diuranthera; Asparagaceae: Asparagus; Asphodelaceae: Aloe, Eremurus; Calochortaceae: Streptopus, Tricyrtis; Colchicaceae: Disporum, Gloriosa, Iphigenia; Convallariaceae: Aspidistra, Campylandra, Convallaria, Disporopsis, Heteropolygonatum, Liriope, Maianthemum, Ophiopogon, Peliosanthes, Poly- gonatum, Reineckea, Rohdea, Speirantha, Theropogon, Tupistra; Dracaenaceae: Dracaena; Hemerocallidaceae: Dianella, Hemerocallis; Hostaceae: Hosta; Hyacinthaceae: Barnardia; Liliaceae: Cardiocrinum, Clintonia, Erythronium, Fritillaria, Gagea, Lilium, Lloydia, Nomocharis, Notholirion, Tulipa; Lomandraceae: Cordyline, Thysanotus; Melanthiaceae: Chionographis, Heloniopsis, Veratrum, Ypsilandra, Zigadenus; Nartheciaceae: Aletris, Petrosavia, Tofieldia; Smilacaceae: Heterosmilax,Smilax; Trilliaceae: Paris, Trillium. The Liliaceae contain many members of economic importance. Notable among them are some species of Allium, Aloe, Fritillaria, Hemerocallis, Lilium, and Tulipa. The genera Ornithogalum Linnaeus, Ruscus Linnaeus, Sansevieria Thunberg, and Yucca Linnaeus are represented in China by introduced, cultivated ornamentals. They were treated in FRPS but are not described in this account. Wang Fa-tsuan & Tang Tsin, eds. 1978; 1980. Liliaceae. Fl. Reipubl. Popularis Sin. 15: 1–280; 14: 1–308. 1a. Herbs saprophytic, without green leaves ........................................................................................................................ 2. Petrosavia 1b. Plants autotrophic, with green leaves. 2a. Plants cormous or bulbiferous. 3a. Plants cormous. 4a. Perianth segments 7–10 × ca. 1 mm, straight; leaves straight at apex ................................................................. 26. Iphigenia 4b. Perianth segments 45–50 × ca. 8 mm, strongly reflexed; leaves with an apical tendril ....................................... 27. Gloriosa 3b. Plants bulbiferous. 5a. Styles 3; anthers reniform, with confluent locules. 6a. Pedicel pubescent; perianth segments not glandular at base ............................................................................... 4. Veratrum 6b. Pedicel glabrous; perianth segments glandular at base ..................................................................................... 5. Zigadenus 5b. Style 1, simple to 3-fid; anthers not reniform, with 2 separate locules. 7a. Inflorescence an umbel, at first wholly enveloped by a scarious spathe ............................................................ 32. Allium 7b. Inflorescence generally not an umbel or, if umbellate, never wholly enveloped by a scarious spathe. 8a. Flowers more than 30, in a dense raceme or spike. 9a. Bulb cylindric; inflorescence spicate; perianth segments partly united; plants with a strong, onionlike odor .................................................................................................................................................................. 33. Milula 9b. Bulb ovoid or globose; inflorescence racemose; perianth segments free; plants without a strong, onionlike odor ............................................................................................................................................. 34. Barnardia 8b. Flowers 1–20, in a lax inflorescence. 10a. Leaves 2, apparently opposite; perianth segments strongly reflexed ................................................. 16. Erythronium 10b. Leaves generally more than 2; perianth segments not reflexed. 11a. Leaves cordate to ovate, reticulate veined .................................................................................... 19. Cardiocrinum 11b. Leaves neither cordate nor ovate, parallel veined. 12a. Bulbs with fleshy, farinaceous scales; perianth segments each with a concave nectary near base adaxially ............................................................................................................................................ 17. Fritillaria 12b. Bulbs without fleshy, farinaceous scales; perianth segments without a concave nectary. 1 Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, 20 Nanxincun, Xiangshan, Beijing 100093, People’s Republic of China. 2 Department of Phytotaxonomy, Institute of Botany, Chinese Academy of Sciences, 20 Nanxincun, Xiangshan, Beijing 100093, People’s Republic of China. 3 Department of Biology, Sichuan University, Chengdu, Sichuan 610064, People’s Republic of China. 4 Botanical Gardens, Graduate School of Science, Osaka City University, 2000 Kisaichi, Katano-shi, Osaka 576-0004, Japan. 13a. Anthers pseudobasifixed; axis of seed usually straight or slightly curved; leaves basal or cauline. 14a. Basal leaves not arising from bulb but from underground stem; bulb more than 1 cm in diam.; perianth more than 2 cm, deciduous after anthesis .......................................................................... 15. Tulipa 14b. Basal leaves arising from bulb; bulb usually 4–5 mm in diam.; perianth less than 2 cm, persistent after anthesis. 15a. Perianth segments ± hardened and enlarged after anthesis, 1.5–2 × as long as capsule ............. 13. Gagea 15b. Perianth segments withered after anthesis, neither hardened nor enlarged, often shorter than capsule ......................................................................................................................................... 14. Lloydia 13b. Anthers dorsifixed and versatile; axis of seed moderately to strongly curved; leaves cauline or at least mostly so. 16a. Bulb with a brown, scarious tunic; bulbels many, around roots; style 3-fid, apically recurved; seeds wingless .......................................................................................................................... 18. Notholirion 16b. Bulb naked; bulbels absent; style apically with 3 stigmatic crests; seeds winged. 17a. Perianth segments similar, usually without spots or blotches ...................................................... 20. Lilium 17b. Inner perianth segments larger than outer ones, generally all segments with dark spots or blotches ................................................................................................................................ 21. Nomocharis 2b. Plants not bulbiferous or cormous, but often producing rhizomes or other underground organs. 18a. Leaves reduced to scales; branchlets becoming leaflike (cladodes), needlelike or linear, 0.2–3 mm wide, numbering several hundred in a single plant ....................................................................................................... 41. Asparagus 18b. Leaves not reduced to scales; branchlets not as above, fewer than 100 in a single plant. 19a. Fruit bursting irregularly at an early stage and exposing seeds; seeds ellipsoid to globose, each resembling a berry or small drupe. 20a. Leaves subplicate veined, with transverse venation between main veins; filaments united into a ring nearly closing mouth of perianth ................................................................................................................ 57. Peliosanthes 20b. Leaves parallel veined, without clear, transverse venation between main veins; filaments not forming a ring. 21a. Leaves longitudinally whitish striped; flowers ± nodding; ovary semi-inferior; filaments much shorter than anthers; seeds blue ........................................................................................................................... 56. Ophiopogon 21b. Leaves not whitish striped; flowers erect or suberect; ovary superior; filaments longer than or as long as anthers; seeds blackish ...............................................................................................................................
Recommended publications
  • Gymnosperms the MESOZOIC: ERA of GYMNOSPERM DOMINANCE
    Chapter 24 Gymnosperms THE MESOZOIC: ERA OF GYMNOSPERM DOMINANCE THE VASCULAR SYSTEM OF GYMNOSPERMS CYCADS GINKGO CONIFERS Pinaceae Include the Pines, Firs, and Spruces Cupressaceae Include the Junipers, Cypresses, and Redwoods Taxaceae Include the Yews, but Plum Yews Belong to Cephalotaxaceae Podocarpaceae and Araucariaceae Are Largely Southern Hemisphere Conifers THE LIFE CYCLE OF PINUS, A REPRESENTATIVE GYMNOSPERM Pollen and Ovules Are Produced in Different Kinds of Structures Pollination Replaces the Need for Free Water Fertilization Leads to Seed Formation GNETOPHYTES GYMNOSPERMS: SEEDS, POLLEN, AND WOOD THE ECOLOGICAL AND ECONOMIC IMPORTANCE OF GYMNOSPERMS The Origin of Seeds, Pollen, and Wood Seeds and Pollen Are Key Reproductive SUMMARY Innovations for Life on Land Seed Plants Have Distinctive Vegetative PLANTS, PEOPLE, AND THE Features ENVIRONMENT: The California Coast Relationships among Gymnosperms Redwood Forest 1 KEY CONCEPTS 1. The evolution of seeds, pollen, and wood freed plants from the need for water during reproduction, allowed for more effective dispersal of sperm, increased parental investment in the next generation and allowed for greater size and strength. 2. Seed plants originated in the Devonian period from a group called the progymnosperms, which possessed wood and heterospory, but reproduced by releasing spores. Currently, five lineages of seed plants survive--the flowering plants plus four groups of gymnosperms: cycads, Ginkgo, conifers, and gnetophytes. Conifers are the best known and most economically important group, including pines, firs, spruces, hemlocks, redwoods, cedars, cypress, yews, and several Southern Hemisphere genera. 3. The pine life cycle is heterosporous. Pollen strobili are small and seasonal. Each sporophyll has two microsporangia, in which microspores are formed and divide into immature male gametophytes while still retained in the microsporangia.
    [Show full text]
  • 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.
    [Show full text]
  • Asphodelus Fistulosus (Asphodelaceae, Asphodeloideae), a New Naturalised Alien Species from the West Coast of South Africa ⁎ J.S
    Available online at www.sciencedirect.com South African Journal of Botany 79 (2012) 48–50 www.elsevier.com/locate/sajb Research note Asphodelus fistulosus (Asphodelaceae, Asphodeloideae), a new naturalised alien species from the West Coast of South Africa ⁎ J.S. Boatwright Compton Herbarium, South African National Biodiversity Institute, Private Bag X7, Claremont 7735, South Africa Department of Botany and Plant Biotechnology, University of Johannesburg, P.O. Box 524, Auckland Park 2006, Johannesburg, South Africa Received 4 November 2011; received in revised form 18 November 2011; accepted 21 November 2011 Abstract Asphodelus fistulosus or onionweed is recorded in South Africa for the first time and is the first record of an invasive member of the Asphodelaceae in the country. Only two populations of this plant have been observed, both along disturbed roadsides on the West Coast of South Africa. The extent and invasive potential of this infestation in the country is still limited but the species is known to be an aggressive invader in other parts of the world. © 2011 SAAB. Published by Elsevier B.V. All rights reserved. Keywords: Asphodelaceae; Asphodelus; Invasive species 1. Introduction flowers (Patterson, 1996). This paper reports on the presence of this species in South Africa. A population of A. fistulosus was The genus Asphodelus L. comprises 16 species distributed in first observed in the early 1990's by Drs John Manning and Eurasia and the Mediterranean (Días Lifante and Valdés, 1996). Peter Goldblatt during field work for their Wild Flower Guide It is superficially similar to the largely southern African to the West Coast (Manning and Goldblatt, 1996).
    [Show full text]
  • Through Our French Window Gordon James
    ©Gordon James ©Gordon Through our French window Gordon James Fig. 1 Asphodelus ramosus n 2014 I wrote an article above the hamlet of Le attention – systematically I for this journal about Clapier where we have a perhaps, dealing with the the orchids that grow on small house, and covers an Ranunculaceae family first, and around a limestone area of perhaps 25km2 lying but that could prove a little plateau in Southern France 750–850m above sea level dull; or perhaps according to called the Plateau du which, together with the season. In the end I decided Guilhaumard, which is surrounding countryside, simply to pick out some of situated on the southern supports an extraordinarily our favourites. With a few edge of the great Causse rich range of plants besides exceptions all the plants du Larzac, a limestone orchids. mentioned in this article karst plateau in the south I wasn’t sure how best can be reached on foot from of the Massif Central. to introduce the plants our house by moderately fit Guilhaumard rises steeply I think deserve special pensioners like us! ©Gordon James ©Gordon James ©Gordon Fig. 2 Asphodelus ramosus Fig. 3 Narcissus assoanus 371 ©Gordon James ©Gordon James ©Gordon Fig. 4 Narcissus poeticus Fig. 5 Iris lutescens Despite its elevation, I will start with those summers are hot, as the plants which, at least for a Plateau is relatively far moment, carpet the ground toward the South of and foremost amongst these ©Gordon James ©Gordon France, though it can be is Asphodelus ramosus (syn. quite cold and snowy A.
    [Show full text]
  • Assessment of Plant Diversity for Threat Elements: a Case Study of Nargu Wildlife Sanctuary, North Western Himalaya
    Ceylon Journal of Science 46(1) 2017: 75-95 DOI: http://doi.org/10.4038/cjs.v46i1.7420 RESEARCH ARTICLE Assessment of plant diversity for threat elements: A case study of Nargu wildlife sanctuary, north western Himalaya Pankaj Sharma*, S.S. Samant and Manohar Lal G.B. Pant National Institute of Himalayan Environment and Sustainable Development, Himachal Unit, Mohal- Kullu-175126, H.P., India Received: 12/07/2016; Accepted: 16/02/2017 Abstract: Biodiversity crisis is being experienced losses, over exploitation, invasions of non-native throughout the world, due to various anthropogenic species, global climate change (IUCN, 2003) and and natural factors. Therefore, it is essential to disruption of community structure (Novasek and identify suitable conservation priorities in biodiversity Cleland, 2001). As a result of the anthropogenic rich areas. For this myriads of conservational pressure, the plant extinction rate has reached approaches are being implemented in various ecosystems across the globe. The present study has to137 species per day (Mora et al., 2011; Tali et been conducted because of the dearth of the location- al., 2015). At present, the rapid loss of species is specific studies in the Indian Himalayas for assessing estimated to be between 1,000–10,000 times the ‘threatened species’. The threat assessment of faster than the expected natural extinction rate plant species in the Nargu Wildlife Sanctuary (NWS) (Hilton-Taylor, 2000). Under the current of the northwest Himalaya was investigated using scenario, about 20% of all species are likely to Conservation Priority Index (CPI) during the present go extinct within next 30 years and more than study.
    [Show full text]
  • State of New York City's Plants 2018
    STATE OF NEW YORK CITY’S PLANTS 2018 Daniel Atha & Brian Boom © 2018 The New York Botanical Garden All rights reserved ISBN 978-0-89327-955-4 Center for Conservation Strategy The New York Botanical Garden 2900 Southern Boulevard Bronx, NY 10458 All photos NYBG staff Citation: Atha, D. and B. Boom. 2018. State of New York City’s Plants 2018. Center for Conservation Strategy. The New York Botanical Garden, Bronx, NY. 132 pp. STATE OF NEW YORK CITY’S PLANTS 2018 4 EXECUTIVE SUMMARY 6 INTRODUCTION 10 DOCUMENTING THE CITY’S PLANTS 10 The Flora of New York City 11 Rare Species 14 Focus on Specific Area 16 Botanical Spectacle: Summer Snow 18 CITIZEN SCIENCE 20 THREATS TO THE CITY’S PLANTS 24 NEW YORK STATE PROHIBITED AND REGULATED INVASIVE SPECIES FOUND IN NEW YORK CITY 26 LOOKING AHEAD 27 CONTRIBUTORS AND ACKNOWLEGMENTS 30 LITERATURE CITED 31 APPENDIX Checklist of the Spontaneous Vascular Plants of New York City 32 Ferns and Fern Allies 35 Gymnosperms 36 Nymphaeales and Magnoliids 37 Monocots 67 Dicots 3 EXECUTIVE SUMMARY This report, State of New York City’s Plants 2018, is the first rankings of rare, threatened, endangered, and extinct species of what is envisioned by the Center for Conservation Strategy known from New York City, and based on this compilation of The New York Botanical Garden as annual updates thirteen percent of the City’s flora is imperiled or extinct in New summarizing the status of the spontaneous plant species of the York City. five boroughs of New York City. This year’s report deals with the City’s vascular plants (ferns and fern allies, gymnosperms, We have begun the process of assessing conservation status and flowering plants), but in the future it is planned to phase in at the local level for all species.
    [Show full text]
  • Nordic Journal of Botany NJB-02477 She, R., Zhao, P
    Nordic Journal of Botany NJB-02477 She, R., Zhao, P. , Zhou, H., Yue, M., Yan, F., Hu, G., Gao, X. and Zhang, S. 2020. Complete chloroplast genomes of Liliaceae (s.l.) species: comparative genomic and phylogenetic analyses. - Nordic Journal of Botany 2019: e02477 Appendix 1 Table A1. List of taxa sampled in this study and species accessions numbers (GenBank). Genus Species Accession number Genus Species Accession number Aletris fauriei KT898912 Polygonatum sibiricum KT695605 Aletris Polygonatum Aletris spicata KT898911 Polygonatum verticillatum KT722981 Allium cepa KM088013 Lilium amabile KY940845 Allium obliquum MG670111 Lilium bakerianum KY748301 Allium Allium prattii MG739457 Lilium brownii KY748296 Allium victorialis MF687749 Lilium bulbiferum MG574829 Amana anhuiensis KY401423 Lilium callosum KY940846 Amana edulis KY401425 Lilium cernuum KX354692 Amana Amana erythronioides KY401424 Lilium distichum KT376489 Amana kuocangshanica KY401426 Lilium duchartrei KY748300 Amana wanzhensis KY401422 Lilium fargesii KX592156 Fritillaria cirrhosa KF769143 Lilium hansonii KM103364 Lilium Fritillaria eduardii MF947708 Lilium henryi KY748302 Fritillaria hupehensis KF712486 Lilium lancifolium KY748297 Fritillaria meleagroides MF947710 Lilium leucanthum KY748299 Fritillaria persica MF947709 Lilium longiflorum KC968977 Fritillaria Fritillaria thunbergii KY646165 Lilium philadelphicum KY940847 Fritillaria unibracteata var. KF769142 Lilium primulinum var. ochraceum KY748298 wabuensis Fritillaria ussuriensis KY646166 Lilium taliense KY009938 Fritillaria
    [Show full text]
  • Index Seminum Et Sporarum Quae Hortus Botanicus Universitatis Biarmiensis Pro Mutua Commutatione Offert
    INDEX SEMINUM ET SPORARUM QUAE HORTUS BOTANICUS UNIVERSITATIS BIARMIENSIS PRO MUTUA COMMUTATIONE OFFERT Salix recurvigemmata A.K. Skvortsov f. variegata Schumikh., O.E. Epanch. & I.V. Belyaeva Biarmiae 2020 Federal State Autonomous Educational Institution of Higher Education «Perm State National Research University», A.G. Genkel Botanical Garden ______________________________________________________________________________________ СПИСОК СЕМЯН И СПОР, ПРЕДЛАГАЕМЫХ ДЛЯ ОБМЕНА БОТАНИЧЕСКИМ САДОМ ИМЕНИ А.Г. ГЕНКЕЛЯ ПЕРМСКОГО ГОСУДАРСТВЕННОГО НАЦИОНАЛЬНОГО ИССЛЕДОВАТЕЛЬСКОГО УНИВЕРСИТЕТА Syringa vulgaris L. ‘Красавица Москвы’ Пермь 2020 Index Seminum 2020 2 Federal State Autonomous Educational Institution of Higher Education «Perm State National Research University», A.G. Genkel Botanical Garden ______________________________________________________________________________________ Дорогие коллеги! Ботанический сад Пермского государственного национального исследовательского университета был создан в 1922 г. по инициативе и под руководством проф. А.Г. Генкеля. Здесь работали известные ученые – ботаники Д.А. Сабинин, В.И. Баранов, Е.А. Павский, внесшие своими исследованиями большой вклад в развитие биологических наук на Урале. В настоящее время Ботанический сад имени А.Г. Генкеля входит в состав регионального Совета ботанических садов Урала и Поволжья, Совет ботанических садов России, имеет статус научного учреждения и особо охраняемой природной территории. Основными научными направлениями работы являются: интродукция и акклиматизация растений,
    [Show full text]
  • Massonia Amoena (Asparagaceae, Scilloideae), a Striking New Species from the Eastern Cape, South Africa
    Phytotaxa 181 (3): 121–137 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2014 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.181.3.1 Massonia amoena (Asparagaceae, Scilloideae), a striking new species from the Eastern Cape, South Africa MARIO MARTÍNEZ-AZORÍN1,2, MICHAEL PINTER1, GERFRIED DEUTSCH1, ANDREAS BRUDERMANN1, ANTHONY P. DOLD3, MANUEL B. CRESPO2, MARTIN PFOSSER4 & WOLFGANG WETSCHNIG1* 1Institute of Plant Sciences, NAWI Graz, Karl-Franzens-University Graz, Holteigasse 6, A-8010 Graz, Austria; e-mail: wolfgang.wet- [email protected] 2CIBIO (Instituto Universitario de la Biodiversidad), Universidad de Alicante, P. O. Box 99, E-03080 Alicante, Spain. 3Selmar Schonland Herbarium, Department of Botany, Rhodes University, Grahamstown 6140 South Africa. 4Biocenter Linz, J.-W.-Klein-Str. 73, A-4040 Linz, Austria. *author for correspondence Abstract As part of an ongoing study towards a taxonomic revision of the genus Massonia Houtt., a new species, Massonia amoena Mart.-Azorín, M.Pinter & Wetschnig, is here described from the Eastern Cape Province of South Africa. This new species is characterized by the leaves bearing heterogeneous circular to elongate pustules and the strongly reflexed perigone seg- ments at anthesis. It is at first sight related to Massonia jasminiflora Burch. ex Baker, M. wittebergensis U.Müll.-Doblies & D.Müll.-Doblies and M. saniensis Wetschnig, Mart.-Azorín & M.Pinter, but differs in vegetative and floral characters, as well as in its allopatric distribution. A complete morphological description of the new species and data on biology, habitat, and distribution are presented. Key words: flora, Hyacinthaceae, Massonieae, Southern Africa, taxonomy Introduction Hyacinthaceae sensu APG (2003) includes ca.
    [Show full text]
  • <I>Chlorophytum Burundiense</I> (Asparagaceae), a New Species
    Plant Ecology and Evolution 144 (2): 233–236, 2011 doi:10.5091/plecevo.2011.609 SHORT COMMUNICATION Chlorophytum burundiense (Asparagaceae), a new species from Burundi and Tanzania Pierre Meerts Herbarium et Bibliothèque de botanique africaine, Université Libre de Bruxelles, Avenue F.D. Roosevelt 50, CP 169, BE-1050 Brussels, Belgium Email: [email protected] Background and aims – In the context of our preparation of the treatment of the genus Chlorophytum for the ‘Flore d’Afrique centrale’, a new species is described from Burundi and Tanzania. Methods – Herbarium taxonomy and SEM of seeds. Key results – Chlorophytum burundiense Meerts sp. nov. is described. It is a small plant < 35 cm in height, with linear leaves < 6 mm wide, a dense raceme and large, deep purplish brown bracts. It is morphologically not closely related to any other species in the genus. It has a distinct habitat, growing in afromontane grassland and scrub at 2000–2500 m a.s.l. All collections but one originate from Burundi, and a single collection originates from SW Tanzania. A determination key is provided for Chlorophytum species with linear leaves occurring in Burundi. Key words – afromontane, determination key, new species, Chlorophytum, SEM, Burundi, Tanzania. INTRODUCTION silvaticum, C. sparsiflorum, C. stolzii, C. subpetiolatum, C. zingiberastrum (taxonomy and nomenclature after Nordal The circumscription of the genus Chlorophytum Ker Gawl. et al. 1997, Kativu et al. 2008). In addition, a species came (Asparagaceae in APG 2009) was revised by Obermeyer to our attention which could not be identified using Baker (1962), Marais & Reilly (1978), Nordal et al. (1990) and (1898), von Poellnitz (1942, 1946), Nordal et al.
    [Show full text]
  • Arils As Food of Tropical American Birds
    Condor, 82:3142 @ The Cooper Ornithological society 1980 ARILS AS FOOD OF TROPICAL AMERICAN BIRDS ALEXANDER F. SKUTCH ABSTRACT.-In Costa Rica, 16 kinds of trees, lianas, and shrubs produce arillate seeds which are eaten by 95 species of birds. These are listed and compared with the birds that feed on the fruiting spikes of Cecropia trees and berries of the melastome Miconia trinervia. In the Valley of El General, on the Pacific slope of southern Costa Rica, arillate seeds and berries are most abundant early in the rainy season, from March to June or July, when most resident birds are nesting and northbound migrants are leaving or passing through. The oil-rich arils are a valuable resource for nesting birds, especially honeycreepers and certain woodpeck- ers, and they sustain the migrants. Vireos are especially fond of arils, and Sulphur-bellied Flycatchers were most numerous when certain arillate seeds were most abundant. Many species of birds take arils from the same tree or vine without serious competition. However, at certain trees with slowly opening pods, birds vie for the contents while largely neglecting other foods that are readily available. Although many kinds of fruits eaten by during the short time that the seed remains birds may be distinguished morphological- in the alimentary tract of a small bird. ly, functionally they fall into two main Wallace (1872) described how the Blue- types, exemplified by the berry and the pod tailed Imperial Pigeon (Duculu concinnu) containing arillate seeds. Berries and ber- swallows the seed of the nutmeg (Myristicu rylike fruits are generally indehiscent; no frugruns) and, after digesting the aril or hard or tough integument keeps animals mace, casts up the seed uninjured.
    [Show full text]
  • Pollen Morphology of Erythronium L. (Liliaceae) and Its Systematic Relationships
    J. Basic. Appl. Sci. Res., 2(2)1833-1838, 2012 ISSN 2090-4304 Journal of Basic and Applied © 2012, TextRoad Publication Scientific Research www.textroad.com Pollen Morphology of Erythronium L. (Liliaceae) and its Systematic Relationships Sayed-Mohammad Masoumi Department of Plant Protection, Razi University, Kermanshah, Iran ABSTRACT Pollen morphology of three genus of Erythronium was studied by the Light Microscopy (LM), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM). Sulcus long reaching the ends of the grains, with operculum (E. giganteum, E. sibiricum) or without it (E. caucasicum). With surface latticed ornamentation and large lattice, thickness of muri and size of Lumina in E. sibiricum are widely varied. Also, most palynomorphological characteristics of the data transmission electron microscopy (TEM) showed no strong differences between E. caucasicum and E. sibiricum, , but these species are well distinguished from E. giganteum according to ectexine thickness (thickness of the tectum and the foot layer), shape and diameter of the caput, height and width of the columella. KEY WORDS: Caput; Columella; Exine ornamentation; intine; Microrelief; Pollen grain; Tectum. INTRODUCTION Takhtajan, 1987 indicated that the genus of Erythronium in Tribe Tulipeae is of the Liliaceae family. Different sources have considered the species number of this genus varied from 24-30. Baranova (1999) introduced 24 species for this genus, of which 20 species were spread in North America. Allen et al. (2003) examined the genus of Erythronium, Amana, and Tulipa using the DNA sequences from the chloroplast gene matK and the internal transcribed spacer (ITS) of nuclear ribosomal DNA. Palynomorphological characters of 20 different pollen species of Erythronium were evaluated by different researchers (Ikuse, 1965; Beug (1963); Radulescu, 1973; Nakamura, 1980; Schulze, 1980; Kuprianova, 1983; Takahashi (1987); Kosenko, 1991b, 1992, 1996, 1999; Maassoumi, 2005a, 2005b, 2007).
    [Show full text]