Orchidaceous Additions to the Philippine Flora (II)
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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. -
The Diversity of Wild Orchids in the Southern Slope of Mount Merapi, Yogyakarta, Indonesia Eight Years After the 2010 Eruption
BIODIVERSITAS ISSN: 1412-033X Volume 21, Number 9, September 2020 E-ISSN: 2085-4722 Pages: 4457-4465 DOI: 10.13057/biodiv/d210964 The diversity of wild orchids in the southern slope of Mount Merapi, Yogyakarta, Indonesia eight years after the 2010 eruption FEBRI YUDA KURNIAWAN1,2,♥, FAUZANA PUTRI2,3, AHMAD SUYOKO2,3, HIMAWAN MASYHURI2,3, MAYA PURQI SULISTIANINGRUM2,3, ENDANG SEMIARTI3,♥♥ 1Postgraduate School, Universitas Gadjah Mada. Jl. Teknika Utara, Sleman 55281, Yogyakarta, Indonesia. Tel./fax. +62-274-544975, email: [email protected] 2Biology Orchid Study Club (BiOSC), Faculty of Biology, Universitas Gadjah Mada. Jl. Teknika Selatan, Sekip Utara, Sleman 55281, Yogyakarta, Indonesia 3Department of Tropical Biology, Faculty of Biology, Universitas Gadjah Mada. Jl. Teknika Selatan, Sekip Utara, Sleman 55281, Yogyakarta, Indonesia. Tel./fax.: +62-274-580839, email: [email protected] Manuscript received: 21 August 2020. Revision accepted: 31 August 2020. Abstract. Kurniawan FY, Putri F, Suyoko A, Masyhuri H, Sulistianingrum MP, Semiarti E. 2020. The diversity of wild orchids in the southern slope of Mount Merapi, Yogyakarta, Indonesia eight years after the 2010 eruption. Biodiversitas 21: 4457-4465. The ecosystem of the slopes of Mount Merapi is mountain tropical forest which is frequently affected by volcanic activities. The dynamics of the volcano affect the diversity and abundance of orchids in the ecosystem. Tritis is an area included in the Turgo Hill of the southern slope of Mount Merapi and is under the management of Mount Merapi National Park. The ecosystem in Tritis area classified as lower mountain forest and it has been affected by Mount Merapi eruption. This study aimed to do an inventory of orchid species in Tritis to know the diversity and abundance of orchids that exist in this area. -
Australia Lacks Stem Succulents but Is It Depauperate in Plants With
Available online at www.sciencedirect.com ScienceDirect Australia lacks stem succulents but is it depauperate in plants with crassulacean acid metabolism (CAM)? 1,2 3 3 Joseph AM Holtum , Lillian P Hancock , Erika J Edwards , 4 5 6 Michael D Crisp , Darren M Crayn , Rowan Sage and 2 Klaus Winter In the flora of Australia, the driest vegetated continent, [1,2,3]. Crassulacean acid metabolism (CAM), a water- crassulacean acid metabolism (CAM), the most water-use use efficient form of photosynthesis typically associated efficient form of photosynthesis, is documented in only 0.6% of with leaf and stem succulence, also appears poorly repre- native species. Most are epiphytes and only seven terrestrial. sented in Australia. If 6% of vascular plants worldwide However, much of Australia is unsurveyed, and carbon isotope exhibit CAM [4], Australia should host 1300 CAM signature, commonly used to assess photosynthetic pathway species [5]. At present CAM has been documented in diversity, does not distinguish between plants with low-levels of only 120 named species (Table 1). Most are epiphytes, a CAM and C3 plants. We provide the first census of CAM for the mere seven are terrestrial. Australian flora and suggest that the real frequency of CAM in the flora is double that currently known, with the number of Ellenberg [2] suggested that rainfall in arid Australia is too terrestrial CAM species probably 10-fold greater. Still unpredictable to support the massive water-storing suc- unresolved is the question why the large stem-succulent life — culent life-form found amongst cacti, agaves and form is absent from the native Australian flora even though euphorbs. -
How to Cite Complete Issue More Information About This Article Journal's Webpage in Redalyc.Org Scientific Information System Re
Lankesteriana ISSN: 1409-3871 Lankester Botanical Garden, University of Costa Rica Pedersen, Henrik Æ.; Find, Jens i.; Petersen, Gitte; seberG, Ole On the “seidenfaden collection” and the multiple roles botanical gardens can play in orchid conservation Lankesteriana, vol. 18, no. 1, 2018, January-April, pp. 1-12 Lankester Botanical Garden, University of Costa Rica DOI: 10.15517/lank.v18i1.32587 Available in: http://www.redalyc.org/articulo.oa?id=44355536001 How to cite Complete issue Scientific Information System Redalyc More information about this article Network of Scientific Journals from Latin America and the Caribbean, Spain and Journal's webpage in redalyc.org Portugal Project academic non-profit, developed under the open access initiative LANKESTERIANA 18(1): 1–12. 2018. doi: http://dx.doi.org/10.15517/lank.v18i1.32587 ON THE “SEIDENFADEN COLLECTION” AND THE MULTIPLE ROLES BOTANICAL GARDENS CAN PLAY IN ORCHID CONSERVATION HENRIK Æ. PEDERSEN1,3, JENS I. FIND2,†, GITTE PETERSEN1 & OLE SEBERG1 1 Natural History Museum of Denmark, University of Copenhagen, Øster Voldgade 5–7, DK-1353 Copenhagen K, Denmark 2 Department of Geosciences and Natural Resource Management, University of Copenhagen, Rolighedsvej 23, DK-1958 Frederiksberg C, Denmark 3 Author for correspondence: [email protected] † Deceased 2nd December 2016 ABSTRACT. Using the “Seidenfaden collection” in Copenhagen as an example, we address the common view that botanical garden collections of orchids are important for conservation. Seidenfaden collected live orchids all over Thailand from 1957 to 1983 and created a traditional collection for taxonomic research, characterized by high taxonomic diversity and low intraspecific variation. Following an extended period of partial neglect, we managed to set up a five-year project aimed at expanding the collection with a continued focus on taxonomic diversity, but widening the geographic scope to tropical Asia. -
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. -
Seidenfaden Malaysia: 0.65 These Figures Are Surprisingly High, They Apply to Single Only. T
BIOGEOGRAPHY OF MALESIAN ORCHIDACEAE 273 VIII. Biogeographyof Malesian Orchidaceae A. Schuiteman Rijksherbarium/Hortus Botanicus, P.O. Box 9514, 2300 RA Leiden, The Netherlands INTRODUCTION The Orchidaceae outnumber far other in Malesia. At how- by any plant family present, accurate estimate of the of Malesian orchid is difficult to make. ever, an number species Subtracting the numberofestablishedsynonyms from the numberof names attributed to Malesian orchid species results in the staggering figure of 6414 species, with a retention of 0.74. This is ratio (ratio of ‘accepted’ species to heterotypic names) undoubtedly a overestimate, of the 209 Malesian orchid have been revised gross as most genera never their entire from availablerevisions estimate realis- over range. Extrapolating to a more tic retention ratio is problematic due to the small number of modern revisions and the different of treated. If look for Malesian of nature the groups we comparison at species wide ofretention ratios: some recently revised groups, we encounter a range Bulbophylluw sect. Uncifera (Vermeulen, 1993): 0.24 Dendrobium sect. Oxyglossum (Reeve & Woods, 1989): 0.24 Mediocalcar (Schuiteman, 1997): 0.29 Pholidota (De Vogel, 1988): 0.29 Bulbophyllum sect. Pelma (Vermeulen, 1993): 0.50 Paphiopedilum (Cribb, 1987, modified): 0.57 Dendrobium sect. Spatulata (Cribb, 1986, modified): 0.60. Correspondingly, we find a wide rangeof estimates for the ‘real’ numberof known Male- sian orchid species: from 2050 to 5125. Another approach would be to look at a single area, and to compute the retention ratio for the orchid flora of that area. If we do this for Java (mainly based on Comber, 1990), Peninsular Malaysia & Singapore (Seidenfaden & Wood, 1992) and Sumatra (J.J. -
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 -
The Genus Liparis Len Field 64
Journal of the Native Orchid Society of South Australia Inc Urochilus (Pterostylis) sanguineus Print Post Approved Volume 28 Nº 6 PP 543662/00018 July 2004 NATIVE ORCHID SOCIETY OF SOUTH AUSTRALIA POST OFFICE BOX 565 UNLEY SOUTH AUSTRALIA 5061 The Native Orchid Society of South Australia promotes the conservation of orchids through the preservation of natural habitat and through cultivation. Except with the documented official representation of the management committee, no person may represent the Society on any matter. All native orchids are protected in the wild; their collection without written Government permit is illegal. PRESIDENT SECRETARY Bodo Jensen: Cathy Houston telephone 8243 0251 work 8347 2005 telephone 8356 7356 VICE PRESIDENT Bob Bates COMMITTEE Peter McCauley Brendan Killen Malcolm Guy David Pettifor EDITOR TREASURER David Hirst Iris Freeman 14 Beaverdale Avenue ASSISTANT TREASURER Windsor Gardens SA 5087 Bill Dear Telephone 8261 7998 telephone 8296 2111 Email [email protected] mobile 0414 633941 LIFE MEMBERS Mr R. Hargreaves† Mr D. Wells Mr H. Goldsack† Mr G. Carne Mr R. Robjohns† Mr R Bates Mr J. Simmons† Mr R Shooter Mr. L. Nesbitt Registrar of Judges: Reg Shooter Trading Table: Judy Penney Field Trips and Conservation: Thelma Bridle telephone 8384 4174 Tuber bank Coordinator: Malcolm Guy telephone 8276 7350 New Members Coordinator: David Pettifor telephone 0416 095095 PATRON Mr T. R. N. Lothian The Native Orchid Society of South Australia, while taking all due care, take no responsibility for loss or damage to any plants whether at shows, meetings or exhibits. Views or opinions expressed by authors of articles within this Journal do not necessarily reflect the views or opinions of the management committee. -
Redalyc.ARE OUR ORCHIDS SAFE DOWN UNDER?
Lankesteriana International Journal on Orchidology ISSN: 1409-3871 [email protected] Universidad de Costa Rica Costa Rica BACKHOUSE, GARY N. ARE OUR ORCHIDS SAFE DOWN UNDER? A NATIONAL ASSESSMENT OF THREATENED ORCHIDS IN AUSTRALIA Lankesteriana International Journal on Orchidology, vol. 7, núm. 1-2, marzo, 2007, pp. 28- 43 Universidad de Costa Rica Cartago, Costa Rica Available in: http://www.redalyc.org/articulo.oa?id=44339813005 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative LANKESTERIANA 7(1-2): 28-43. 2007. ARE OUR ORCHIDS SAFE DOWN UNDER? A NATIONAL ASSESSMENT OF THREATENED ORCHIDS IN AUSTRALIA GARY N. BACKHOUSE Biodiversity and Ecosystem Services Division, Department of Sustainability and Environment 8 Nicholson Street, East Melbourne, Victoria 3002 Australia [email protected] KEY WORDS:threatened orchids Australia conservation status Introduction Many orchid species are included in this list. This paper examines the listing process for threatened Australia has about 1700 species of orchids, com- orchids in Australia, compares regional and national prising about 1300 named species in about 190 gen- lists of threatened orchids, and provides recommen- era, plus at least 400 undescribed species (Jones dations for improving the process of listing regionally 2006, pers. comm.). About 1400 species (82%) are and nationally threatened orchids. geophytes, almost all deciduous, seasonal species, while 300 species (18%) are evergreen epiphytes Methods and/or lithophytes. At least 95% of this orchid flora is endemic to Australia. -
A Review of CITES Appendices I and II Plant Species from Lao PDR
A Review of CITES Appendices I and II Plant Species From Lao PDR A report for IUCN Lao PDR by Philip Thomas, Mark Newman Bouakhaykhone Svengsuksa & Sounthone Ketphanh June 2006 A Review of CITES Appendices I and II Plant Species From Lao PDR A report for IUCN Lao PDR by Philip Thomas1 Dr Mark Newman1 Dr Bouakhaykhone Svengsuksa2 Mr Sounthone Ketphanh3 1 Royal Botanic Garden Edinburgh 2 National University of Lao PDR 3 Forest Research Center, National Agriculture and Forestry Research Institute, Lao PDR Supported by Darwin Initiative for the Survival of the Species Project 163-13-007 Cover illustration: Orchids and Cycads for sale near Gnommalat, Khammouane Province, Lao PDR, May 2006 (photo courtesy of Darwin Initiative) CONTENTS Contents Acronyms and Abbreviations used in this report Acknowledgements Summary _________________________________________________________________________ 1 Convention on International Trade in Endangered Species (CITES) - background ____________________________________________________________________ 1 Lao PDR and CITES ____________________________________________________________ 1 Review of Plant Species Listed Under CITES Appendix I and II ____________ 1 Results of the Review_______________________________________________________ 1 Comments _____________________________________________________________________ 3 1. CITES Listed Plants in Lao PDR ______________________________________________ 5 1.1 An Introduction to CITES and Appendices I, II and III_________________ 5 1.2 Current State of Knowledge of the