The Genus Liparis Len Field 64
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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. -
75. LIPARIS Richard, De Orchid. Eur. 21, 30, 38. 1817, Nom. Cons. 羊耳蒜属 Yang Er Suan Shu Chen Xinqi (陈心启 Chen Sing-Chi); Paul Ormerod, Jeffrey J
Flora of China 25: 211–228. 2009. 75. LIPARIS Richard, De Orchid. Eur. 21, 30, 38. 1817, nom. cons. 羊耳蒜属 yang er suan shu Chen Xinqi (陈心启 Chen Sing-chi); Paul Ormerod, Jeffrey J. Wood Alipsa Hoffmannsegg; Anistylis Rafinesque; Diteilis Rafinesque; Dituilis Rafinesque; Empusa Lindley; Empusaria Reichen- bach; Iebine Rafinesque; Leptorkis Thouars; Malaxis sect. Platystylis Blume; Mesoptera Rafinesque; Paliris Dumortier; Platystylis (Blume) Lindley (1830), not Sweet (1828); Pseudorchis Gray (1821), not Séguier (1754); Sturmia Reichenbach (1826), not Hoppe (1799). Herbs, terrestrial, lithophytic, or epiphytic, rhizomatous, rarely mycotrophic and leaves reduced to scales. Stems pseudobulbous, sometimes appearing as a many-noded, fleshy stem, clustered or not, when young covered by sterile bracts. Leaves 1 to several, linear to ovate or elliptic, plicate or not, thinly textured to leathery, basal or cauline (terrestrial species), or arising from apex or sub- terminal nodes of pseudobulbs (epiphytic species), articulate or not at base. Inflorescences erect to pendulous, racemose, laxly or densely many flowered; floral bracts persistent, small. Flowers small or medium-sized, yellow, green, orange, or purple, often translucent, usually resupinate. Sepals spreading, dorsal sepal free, lateral sepals sometimes fused for part or all of their length. Petals free, often reflexed, often linear and unlike sepals; lip often reflexed, ovate, oblong, or flabellate, entire or lobed, usually with a basal callus, lacking a spur. Column incurved-arcuate, clavate, long, winged at apex and sometimes at base; anther cap attached by a slen- der filament, 2-locular; pollinia 4 in 2 pairs, waxy, ovoid, bilaterally flattened, each pair with a small viscidium; rostellum thinly textured, blunt. -
A Monograph of the Genus Liparis
245% MR. H. N. EIDLEY’S MONOQEAPB A Monograph of‘the Genus Liparis. By H. N. RIDLEY,M.A., F.L.S. [Read 3rd June, 1886.1 ALTHOUQH the literature treating of Orchids is very extensive, and is still very largely on the increase, the number of Mono- graphs of genera is remarkably small, and, indeed, it seems that there is no Order of equal size and importance now so meagrely provided ‘for in this respect. Species innumerable have been described as they were discovered or introduced into cultivation, often several species of different genera together, and that with- out correlation or comparison with other species. The result of this is that the species of many genera are inextricably confused, and it, is by no means easy, even with a great deal of labour, to collate all the described species of any large genus. It not un- frequently happens also that plants are introduced, perhaps almost accidentally, into cultivation, and shortly after dying out are entirely lost, no specimens having been preserved, and only a description, often, especially among the older writers, of an in- sufficient character, by which the species can be identified. I have therefore thought it may be useful to those interested in this group of plants to collect what information I could glean concerning the genus Liparis into a single paper. No list has been published of the genus since the publication of the ‘ Cfenera and Species of the Orchidaceous Plants,’ by Lindley in 1840, in which thirty-three species are described, while the number of species at present known is above 100. -
Ogasawara) Archipelago, Japan, and Its Identification Using Molecular Sequences from a Herbarium Specimen Collected More Than 100 Years Ago
ISSN 1346-7565 Acta Phytotax. Geobot. 70 (3): 149–158 (2019) doi: 10.18942/apg.201901 Rediscovery of Liparis hostifolia (Orchidaceae) on Minami-iwo-to Island in the Bonin (Ogasawara) Archipelago, Japan, and its Identification Using Molecular Sequences from a Herbarium Specimen Collected more than 100 Years Ago 1,† 2,† 3 4 Koji TaKayama , Chie TsuTsumi , Dairo KawaguChi , hiDeToshi KaTo anD 2,* Tomohisa yuKawa 1Department of Botany, Graduate School of Science, Kyoto University, Kitashirakawa Oiwake-cho, Sakyo-ku, Kyoto 606-8502, Japan; 2 Department of Botany, National Museum of Nature and Science, 4-1-1 Amakubo, Tsukuba 305- 0005, Japan. *[email protected] (author for correspondence); 3 Ogasawara Islands Branch Office, Tokyo Metropolitan Government, Nishimachi, Chichi-jima, Ogasawara-mura, Tokyo 100-2101, Japan; 4 Department of Biological Sciences, Tokyo Metropolitan University, 1-1 Minami Osawa, Hachioji, Tokyo 192-0397, Japan. † These authors contributed equally to this work Liparis hostifolia (Orchidaceae) on Minami-iwo-to Island in the Bonin (Ogasawara) Archipelago was rediscovered for the first time in 79 years during a field survey in 2017. Its identity was confirmed by morphological comparison and DNA extractions from herbarium specimens collected between 1914 and 1938. Results from the molecular phylogenetic analyses demonstrated that L. hostifolia belongs to the L. makinoana complex. In comparison with other members of the L. makinoana complex, the broadly ovate labellum, short dormancy period, and flowering from November to March are unique characteristics of L. hostifolia. Results from the molecular phylogenetic analyses also suggested that L. hostifolia has had a long-isolated history in the Bonin Archipelago and probably migrated from temperate East Asia. -
Orchid Historical Biogeography, Diversification, Antarctica and The
Journal of Biogeography (J. Biogeogr.) (2016) ORIGINAL Orchid historical biogeography, ARTICLE diversification, Antarctica and the paradox of orchid dispersal Thomas J. Givnish1*, Daniel Spalink1, Mercedes Ames1, Stephanie P. Lyon1, Steven J. Hunter1, Alejandro Zuluaga1,2, Alfonso Doucette1, Giovanny Giraldo Caro1, James McDaniel1, Mark A. Clements3, Mary T. K. Arroyo4, Lorena Endara5, Ricardo Kriebel1, Norris H. Williams5 and Kenneth M. Cameron1 1Department of Botany, University of ABSTRACT Wisconsin-Madison, Madison, WI 53706, Aim Orchidaceae is the most species-rich angiosperm family and has one of USA, 2Departamento de Biologıa, the broadest distributions. Until now, the lack of a well-resolved phylogeny has Universidad del Valle, Cali, Colombia, 3Centre for Australian National Biodiversity prevented analyses of orchid historical biogeography. In this study, we use such Research, Canberra, ACT 2601, Australia, a phylogeny to estimate the geographical spread of orchids, evaluate the impor- 4Institute of Ecology and Biodiversity, tance of different regions in their diversification and assess the role of long-dis- Facultad de Ciencias, Universidad de Chile, tance dispersal (LDD) in generating orchid diversity. 5 Santiago, Chile, Department of Biology, Location Global. University of Florida, Gainesville, FL 32611, USA Methods Analyses use a phylogeny including species representing all five orchid subfamilies and almost all tribes and subtribes, calibrated against 17 angiosperm fossils. We estimated historical biogeography and assessed the -
Liparis Cordifolia Var. Gongshanensis (Orchidaceae, Malaxideae), a New Variety from Yunnan, China
Liparis cordifolia var. gongshanensis (Orchidaceae, Malaxideae), a New Variety from Yunnan, China Jin Xiaohua Herbarium (PE), Institute of Botany, Chinese Academy of Sciences, 20 Nanxinchun, Xiangshan, Beijing 100093, People’s Republic of China. [email protected] ABSTRACT . Liparis cordifolia Hook. f. var. gongsha- 1. Liparis cordifolia Hook. f., Icon. Pl. ser. 3(19): nensis X. H. Jin (Orchidaceae, Malaxideae) is tab. 1811. 1889. TYPE: India. Kashia, Hooker & described from Yunnan, China. It differs from the Thomson 8 (lectotype, designated here, K). typical variety by having larger flowers with the sepals Pearce and Cribb (2002) listed three syntypes of and petals ca. 1.1 cm long (vs. 0.8–0.9 cm in variety Liparis cordifolia, one of which is designated here as cordifolia) and a circular, ciliate lip with a pair of lectotype for this widespread and somewhat polymor- small calli at the base (vs. lip obovate-deltoid, entire, phic species. and ecallose in variety cordifolia). The new variety appears to be restricted to evergreen humid forest in the Dulong River valley (upper portion of the 1a. Liparis cordifolia var. cordifolia. Irrawaddy River), from Yunnan, China. A lectotype 1b. Liparis cordifolia var. gongshanensis X. H. Jin, is designated for L. cordifolia. var. nov. TYPE: China. Yunnan: Gongshan Co., Key words: China, IUCN Red List, Liparis, Mal- Dulong Distr., in forest, 2400 m, 24 June 2008 axideae, Orchidaceae. (fl.), X. H. Jin 9589 (holotype, PE). Figure 1. The genus Liparis Rich. s.l. (Orchidaceae, Malax- Haec varietas a Liparide cordifolia Hook. f. var. cordifolia ideae) consists of 150 to 320 species distributed in the bracteis lanceolatis longioribus, floribus majoribus sepalis tropics worldwide as well as in temperate regions petalis et labello ca. -
Indian Floriculture & Orchid Potential of North East India
ORCHIDS: COMMERCIAL PROSPECTS Courtesy: Dr. R. P. Medhi, Director National Research Centre for Orchids Pakyong, East Sikkim ORCHID FLOWER-UNIQUENESS INDIA FAVORING ORCHIDS Total land area of India - 329 million hectare. India is situated between 6o45’-37 o6’N latitude 68o7’-97o25’E longitudes. The distribution pattern reveals five major plant geographical regions viz., o North Eastern Himalayas o Peninsular region o Western Himalayas o Westerns Ghats and o Andaman and Nicobar group of Islands ORCHID RESOURCES OF INDIA (Number of Species-total) 1000 900 800 700 600 500 400 No. of species No. 300 200 100 0 Himalayan Eastern Peninsular Central Andaman mountain Himalayas India India & and region Gangetic Nicobar plains Islands Regions STATE WISE ORCHID DISTRIBUTION IN INDIA Name of the State Orchids (Number) Name of the Orchids (Number) State Genus Species Genus Species Andaman & Nicobar Group of Islands 59 117 Maharashtra 34 110 Andhra Pradesh 33 67 Manipur 66 251 Arunachal Pradesh 133 600 Meghalaya 104 352 Assam 75 191 Mizoram 74 246 Bihar (incl. Jharkhand) 36 100 Nagaland 63 241 Chhatisgarh 27 68 Orissa 48 129 Goa, Daman & Diu 18 29 Punjab 12 21 Gujrat 10 25 Rajasthan 6 10 Haryana 3 3 Sikkim 122 515 Himachal Pradesh 24 62 Tamil Nadu 67 199 Jammu & Kashmir 27 51 Tripura 34 48 Karnataka 52 177 Uttaranchal 72 237 Kerela 77 230 Uttar Pradesh 19 30 Madhya Pradesh (inc. Chhattisgarh) 34 89 ORCHID RESOURCES OF INDIA (Endemic) 6 15 13 10 76 88 N.E. INDIA E. INDIA W. INDIA PENINSULAR INDIA W. HIMALAYAS ANDAMANS ORCHID RESOURCES OF INDIA (Endangered) 52 34 25 105 44 N.E. -
Graptophyllum Spinigerum F
Bibliography of Pacific and Malesian plant maps of Phanerogams. Fourth Supplement M.M.J. van Balgooy ACANTHACEAE Acanthus A.G. Wells in H.J. Teas, Biol. & Ecol. of Mangroves (1983) 60. Partial (2 spp.); Australia; localities indicated; occasional. A. ilicifolius L. & A. ebracteatus Vahl R.M. Barker, J. Adel. Bot. Gard. 9 (1986) 69, fig. 6. Partial; Australia, New Guinea; localities indicated;partial revision. Asystasia australasica F.M. Bailey R.M. Barker, J. Adel. Bot. Gard. 9 (1986) 135, fig. 21. Complete; S. New Guinea + Torres Strait Islands; localities indicated; partialrevision. Brunoniella acaulis (R.Br.) Bremek. R.M. Barker, J. Adel. Bot. Gard. 9 (1986) 101, fig. 12. Complete; Australia, New Guinea; localities indicated; partial revision. Dicliptera ciliata Decne R.M. Barker, J. Adel. Bot. Gard. 9 (1986) 180, fig. 32. Partial;Australia, New Guinea; localities indicated;partial revision. Dipteracanthus bracteatus (R.Br.) Nees R.M. Barker, J. Adel. Bot. Gard. 9 (1986) 94, fig. 10. Complete; Australia, New Guinea; localities indicated;partial revision. Graptophyllum spinigerum F. Muell. R.M. Barker, J. Adel. Bot. Gard. 9 (1986) 160, fig. 26. Complete; Australia, New Guinea; localities indicated;partial revision. Hygrophila angustifolia R.Br. R.M. Barker, J. Adel. Bot. Gard. 9 (1986) 122, fig. 18. Complete; Australia, New Guinea; localities indicated;partial revision. H. triflora (Roxb.) Fosb. & Sachet R.M. Barker, J. Adel. Bot. Gard. 9 (1986) 122, fig. 18. Partial; Australia, New Guinea (intr.); localities indicated; partial revision. *) As in the previous supplement, author names of taxa are added only if they are cited by the author of the paper concerned. -
Cunninghamia Date of Publication: April 2020 a Journal of Plant Ecology for Eastern Australia
Cunninghamia Date of Publication: April 2020 A journal of plant ecology for eastern Australia ISSN 0727- 9620 (print) • ISSN 2200 - 405X (Online) A Systematic Flora Survey, Floristic Classification and High-Resolution Vegetation Map of Lord Howe Island Paul Sheringham 1*, Peter Richards2, Phil Gilmour3, Jill Smith1 and Ernst Kemmerer 4 1 Department of Planning, Industry and Environment, Locked Bag 914 COFFS HARBOUR NSW 2450 2 17 Coronation Avenue, SAWTELL NSW 2452 3 523 Roses Rd, GLENIFFER, NSW 2454 4 Cradle Coast NRM, PO Box 338, BURNIE TAS 7320 * Author for correspondence: [email protected] Abstract: The present study took advantage of the availability of high resolution ADS40 digital imagery to 1) systematically resample the vegetation of the Lord Howe Island Group (LHIG, excluding Ball’s Pyramid); 2) conduct a numerical analysis of the floristic data; 3) map vegetation extent and the distribution of vegetation communities and 4) compare the resultant classification and mapping with those of Pickard (1983). In July 2013, a total of 86 full floristic and 105 rapid floristic sites were sampled across the island, based on a stratified random sampling design. A hierarchical agglomerative clustering strategy (Flexible UPGMA) and Bray-Curtis dissimilarity coefficient with default beta, along with nearest neighbour analysis to identify anomalous site allocations, was used to analyze the floristic data. In total 33 vegetation communities were delineated and mapped: 19 mapping units from the full floristic analysis; 7 variants identified within five of the above 19 groups; 3 mapping units from analysis of canopy- only floristic data; and 4 mapping units recognised in previous studies that are mapped but were not sampled in this survey. -
Liparis Loeselii
Liparis loeselii Status Annexes II(b) and IV(b) of the EC Habitats Directive, Schedule 4 of the Conservation (Natural Habitats, etc.) Regulations 1994. Labellum Schedule 8, Wildlife & Countryside Act (1981). IUCN Threat category: Endangered (2005). UK Biodiversity Action Plan Priority species. Taxonomy Magnoliopsida: Orchidaceae Scientific name: Liparis loeselii (L.) Rich., Synonymy: Ophrys loeselii L. Common names: Fen Orchid, Gefell-lys y Fignen Liparis loeselii is a distinctive member of the Orchid family (Orchidaceae), and is the only representative in Britain of the genus, which is composed of about 250 species mostly distributed in temperate and tropical regions. Liparis in Europe usually has two basal tubers (mother and daughter) side by side, two leaves, the labellum (or main lip) of the flower turned upwards, downwards or in intermediate directions, and no spur. Basal tuber There are two varieties of L. loeselii in Britain, which are easily distinguished by leaf shape and habitat (Rose 1997): Var. loeselii: Leaves oblong-elliptic (Figure 2a); up to 12 flowers. Fens and reed swamp, mainly East Anglia. Var. ovata Ridd. ex Godfery: Leaves ovate to Figure 1. Illustration of key features (from J. E. Smith & J. broadly elliptical (Figure 2b); up to 6(-10) Sowerby (1852). English Botany. London) flowers. Dune slacks, mainly western Britain. Kay & John (1995) found no genetic variation in the It declined markedly in both areas due to habitat loss, small number of samples studied. drainage, scrub invasion, cessation of peat cutting, and stabilisation of dunes. Distribution & Ecology This rare species is recorded from both sides of the Identification & Field survey Bristol Channel and East Anglia. -
An Annotated Checklist of the Orchids of Sri Lanka, by Fernando And
Rheedea Vol. 18(1) 1-28 2008 An Annotated Checklist of the Orchids of Sri Lanka 1 Samantha Suranjan Fernando and Paul Ormerod Post Graduate Institute of Science, University of Peradeniya, Peradeniya, Sri Lanka. E-mail: [email protected] 1P.O. Box 8210, Cairns 4870, Queensland, Australia. E-mail: [email protected] Abstract A general description of Sri Lanka and its bioclimatic zones are presented. The history of the Island’s orchid taxonomy is briefly reviewed. An updated checklist is presented for the country’s orchid flora using recent information. New species, new records and nomenclatural changes from previous lists are annotated with appropriate references. This work lists 188 species belonging to 78 genera with one endemic genus (Adrorhizon Hook. f.) and 55 endemic species. A new name, Bulbophyllum jayaweerae Fernando et Ormerod, is proposed for Cirrhopetalum roseum Jayaweera. Illegitimacy of the name Saccolabium virescens Gardner ex Lindl. is discussed and this species is described as a new taxon, Robiquetia virescens Ormerod et Fernando. Keywords: Sri Lanka, Orchids, Bulbophyllum jayaweerae, Robiquetia virescens, New name, New taxon Introduction Sri Lanka is a pear shaped island in the Indian Ocean lying in the southern tip of the Indian Peninsula (Fig. 1). It lies between 5° 55’ - 9°51’ North latitudes and 79° 41’ - 81°54’ East longitudes and covers a total area of 65,609.8 km² consisting of 64,453.6 km² of land area and 1,156. 2 km² of inland waters. The island has a maximum length of about 435 km and a maximum width of about 225 km. -
Species Diversity of Orchids in Bukit Barisan Selatan National Park, Lampung, Indonesia
BIODIVERSITAS ISSN: 1412-033X Volume 20, Number 1, January 2019 E-ISSN: 2085-4722 Pages: 343-349 DOI: 10.13057/biodiv/d200140 Species diversity of Orchids in Bukit Barisan Selatan National Park, Lampung, Indonesia ESTI MUNAWAROH♥, YUZAMMI♥♥ Center for Plant Conservation Botanic Gardens, Indonesia Institut of Sciences. Jl. Ir. H. Juanda 13, Bogor 16122, West Java, Indonesia Tel./fax. +62-251-8322187 ♥email: [email protected] ♥♥ [email protected] Manuscript received: 28 September 2018. Revision accepted: 30 December 2018. Abstract. Munawaroh E, Yuzammi. 2019. Species diversity of Orchids in Bukit Barisan Selatan National Park, Lampung, Indonesia. Biodiversitas 20: xxxx. Orchids, belonging to the family Orchidaceae, are well known ornamental plants due to their beautiful flowers and varied colors. The members of this family have received more scientific attention than other plant families because of their unique botanical features and economic value. This study was conducted to explore and record the species diversity of Orchidaceae in Sumatera, especially in the Bukit Barisan Selatan National Park (BBSNP), Lampung, Indonesia. This research was carried out from 2011 to 2014 at four locations, namely Kubu Perahu Resort, Sukaraja Atas Resort, Pugung Tampak Resort and Sekincau Resort, using purposive sampling method. A total of 132 species belonging to 52 genera of orchids have been identified from BBSNP, Lampung, of which 37 genera are epiphytic orchids and 15 genera are terrestrial orchids. Two species namely, Vanda sumatrana and Grammatophyllum speciosum, have been recognized as protected species. Vanda sumatrana is also endemic to Sumatera. These orchids are also cultivated at Liwa Botanic Garden, as an ex situ conservation.