The Araceae of Borneo-The Genera
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Interior Plants: Selection and Care
AZ1025 Interior Plants: Selection and Care 5/98 ELIZABETH D AVISON Some may be purchased at relatively low cost from garden Lecturer, Plant Sciences centers or from garden catalogs. Their readings of Low, Medium and High can give “ballpark figures,” and they can eliminate much of the guesswork in selecting plants (originally authored by Dr. Charles Sacamano, Extension that are adapted to light levels in a given location. Horticulture Specialist, and Dr. Douglas A. Bailey, If sunlight is the major light source you may determine Assistant Professor, Plant Sciences) which category your indoor location falls into by using the following descriptions: Almost any indoor environment is more pleasant and High Light: areas within four feet of large south-east or attractive when living plants are a part of the setting. In west facing windows. apartments, condominiums and single family residences, plants add warmth, personality and year-round beauty. Medium Light: locations in a range of four to eight feet Shopping centers, hotels and resorts take full advantage of from south and east windows and west windows that the colorful, relaxed atmosphere created by green growing do not receive direct sun. things. Offices, banks and other commercial buildings rely Low Light: areas more than eight feet from windows as in on interior plants to humanize the work environment and the center of a room, a hallway or an inside wall. increase productivity. Northern exposures often fall into this category, even There are other important, often overlooked functions close to the window. Many locations that receive only performed by indoor plants. These include directing or artificial light are also low light situations. -
Araceae) in Bogor Botanic Gardens, Indonesia: Collection, Conservation and Utilization
BIODIVERSITAS ISSN: 1412-033X Volume 19, Number 1, January 2018 E-ISSN: 2085-4722 Pages: 140-152 DOI: 10.13057/biodiv/d190121 The diversity of aroids (Araceae) in Bogor Botanic Gardens, Indonesia: Collection, conservation and utilization YUZAMMI Center for Plant Conservation Botanic Gardens (Bogor Botanic Gardens), Indonesian Institute of Sciences. Jl. Ir. H. Juanda No. 13, Bogor 16122, West Java, Indonesia. Tel.: +62-251-8352518, Fax. +62-251-8322187, ♥email: [email protected] Manuscript received: 4 October 2017. Revision accepted: 18 December 2017. Abstract. Yuzammi. 2018. The diversity of aroids (Araceae) in Bogor Botanic Gardens, Indonesia: Collection, conservation and utilization. Biodiversitas 19: 140-152. Bogor Botanic Gardens is an ex-situ conservation centre, covering an area of 87 ha, with 12,376 plant specimens, collected from Indonesia and other tropical countries throughout the world. One of the richest collections in the Gardens comprises members of the aroid family (Araceae). The aroids are planted in several garden beds as well as in the nursery. They have been collected from the time of the Dutch era until now. These collections were obtained from botanical explorations throughout the forests of Indonesia and through seed exchange with botanic gardens around the world. Several of the Bogor aroid collections represent ‘living types’, such as Scindapsus splendidus Alderw., Scindapsus mamilliferus Alderw. and Epipremnum falcifolium Engl. These have survived in the garden from the time of their collection up until the present day. There are many aroid collections in the Gardens that have potentialities not widely recognised. The aim of this study is to reveal the diversity of aroids species in the Bogor Botanic Gardens, their scientific value, their conservation status, and their potential as ornamental plants, medicinal plants and food. -
2007 Vol. 10, Issue 1
Department of Botany & the U.S. National Herbarium TheThe PlantPlant PressPress New Series - Vol. 10 - No. 1 January-March 2007 Botany Profile Taking Aim at the GSPC Targets By Gary A. Krupnick and W. John Kress n 2002, the Convention on Biologi- are the contributions that the Department The data and images of more than cal Diversity (CBD), a global treaty has made towards achieving the 16 targets 95,000 type specimens of algae, Isigned by 188 countries addressing since the Strategy’s inception in 2002. lichens, bryophytes, ferns, gymno- the conservation and sustainable use of sperms and angiosperms are available on biological diversity, adopted the Global Understanding and Documenting Plant USNH’s Type Specimen Register at Strategy for Plant Conservation (GSPC), Diversity <http://ravenel.si.edu/botany/types/>. A the first CBD document that defines Target 1: A widely accessible working multi-DVD set containing images of specific targets for conserving plant list of known plant species, as a step 89,000 vascular type specimens from diversity. The 16 targets are grouped towards a complete world flora USNH has been produced and distrib- under five major headings: (a) under- uted to institutions around the world. In standing and documenting plant diversity; One of the Department’s core mis- addition, data from 778,054 specimen (b) conserving plant diversity; (c) using sions is to discover and describe plant life records have been inventoried in the plant diversity sustainably; (d) promoting in marine and terrestrial environments. EMu catalogue software. education and awareness about plant Thus, one primary objective is to conduct In addition, USNH is a partner in diversity; and (e) building capacity for field work in poorly known areas of high producing the Global Working Check- the conservation of plant diversity. -
CGGJ Vansteenis
BIBLIOGRAPHY : ALGAE 3957 X. Bibliography C.G.G.J. van Steenis (continued from page 3864) The entries have been split into five categories: a) Algae — b) Fungi & Lichens — c) Bryophytes — d) Pteridophytes — e) Spermatophytes 8 General subjects. — Books have been marked with an asterisk. a) Algae: ABDUS M & Ulva a SALAM, A. Y.S.A.KHAN, patengansis, new species from Bang- ladesh. Phykos 19 (1980) 129-131, 4 fig. ADEY ,w. H., R.A.TOWNSEND & w„T„ BOYKINS, The crustose coralline algae (Rho- dophyta: Corallinaceae) of the Hawaiian Islands. Smithson„Contr„ Marine Sci. no 15 (1982) 1-74, 47 fig. 10 new) 29 new); to subfamilies and genera (1 and spp. (several key genera; keys to species„ BANDO,T„, S.WATANABE & T„NAKANO, Desmids from soil of paddyfields collect- ed in Java and Sumatra. Tukar-Menukar 1 (1982) 7-23, 4 fig. 85 species listed and annotated; no novelties. *CHRISTIANSON,I.G., M.N.CLAYTON & B.M.ALLENDER (eds.), B.FUHRER (photogr.), Seaweeds of Australia. A.H.& A.W.Reed Pty Ltd., Sydney (1981) 112 pp., 186 col.pl. Magnificent atlas; text only with the phyla; ample captions; some seagrasses included. CORDERO Jr,P.A„ Studies on Philippine marine red algae. Nat.Mus.Philip., Manila (1981) 258 pp., 28 pi., 1 map, 265 fig. Thesis (Kyoto); keys and descriptions of 259 spp„, half of them new to the Philippines; 1 new species. A preliminary study of the ethnobotany of Philippine edible sea- weeds, especially from Ilocos Norte and Cagayan Provinces. Acta Manillana A 21 (31) (1982) 54-79. Chemical analysis; scientific and local names; indication of uses and storage. -
Araceae), with P
bioRxiv preprint doi: https://doi.org/10.1101/2020.10.05.326850; this version posted October 7, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Taxonomic revision of the threatened African genus Pseudohydrosme Engl. (Araceae), with P. ebo, a new, Critically Endangered species from Ebo, Cameroon. Martin Cheek¹, Barthelemy Tchiengue2, Xander van der Burgt¹ ¹Science, Royal Botanic Gardens, Kew, Richmond, Surrey, U.K. 2 IRAD-Herbier National Camerounais, Yaoundé, BP 1601, Cameroon Corresponding author: Martin Cheek¹ Email address: [email protected] ABSTRACT This is the first revision in nearly 130 years of the African genus Pseudohydrosme, formerly considered endemic to Gabon. Sister to Anchomanes, Pseudohydrosme is distinct from Anchomanes because of its 2–3-locular ovary (not unilocular), peduncle concealed by cataphylls at anthesis and far shorter than the spathe (not exposed, far exceeding the spathe), stipitate fruits and viviparous (vegetatively apomictic) roots (not sessile, roots non-viviparous). Three species, one new to science, are recognised, in two sections. Although doubt has previously been cast on the value of recognising Pseudohydrosme buettneri, of Gabon, it is here accepted and maintained as a distinct species in the monotypic section, Zyganthera. However, it is considered to be probably globally extinct. Pseudohydrosme gabunensis, type species of the genus, also Gabonese, is maintained in Sect. Pseudohydrosme together with Pseudohydrosme ebo sp.nov. of the Ebo Forest, Littoral, Cameroon, the first addition to the genus since the nineteenth century, and which extends the range of the genus 450 km north from Gabon, into the Cross-Sanaga biogeographic area. -
Giant Swamp Taro, a Little-Known Asian-Pacific Food Crop Donald L
36 TROPICAL ROOT CROPS SYMPOSIUM Martin, F. W., Jones, A., and Ruberte, R. M. A improvement of yams, Dioscorea rotundata. wild Ipomoea species closely related to the Nature, 254, 1975, 134-135. sweet potato. Ec. Bot. 28, 1974,287-292. Sastrapradja, S. Inventory, evaluation and mainte Mauny, R. Notes historiques autour des princi nance of the genetic stocks at Bogor. Trop. pales plantes cultiVl!es d'Afrique occidentale. Root and Tuber Crops Tomorrow, 2, 1970, Bull. Inst. Franc. Afrique Noir 15, 1953, 684- 87-89. 730. Sauer, C. O. Agricultural origins and dispersals. Mukerjee, I., and Khoshoo, T. N. V. Genetic The American Geogr. Society, New York, 1952. evolutionary studies in starch yielding Canna Sharma, A. K., and de Deepesh, N. Polyploidy in edulis. Gen. Iber. 23, 1971,35-42. Dioscorea. Genetica, 28, 1956, 112-120. Nishiyama. I. Evolution and domestication of the Simmonds, N. W. Potatoes, Solanum tuberosum sweet potato. Bot. Mag. Tokyo, 84, 1971, 377- (Solanaceae). In Simmonds, N. W., ed., Evolu 387. tion of crop plants. Longmans, London, 279- 283, 1976. Nishiyama, I., Miyazaki, T., and Sakamoto, S. Stutervant, W. C. History and ethnography of Evolutionary autoploidy in the sweetpotato some West Indian starches. In Ucko, J. J., and (Ipomea batatas (L). Lam.) and its preogenitors. Dimsley, G. W., eds., The domestication of Euphytica 24, 1975, 197-208. plants and animals. Duckworth, London, 177- Plucknett, D. L. Edible aroids, A locasia, Colo 199, 1969. casia, Cyrtosperma, Xanthosoma (Araceae). In Subramanyan, K. N., Kishore, H., and Misra, P. Simmonds, N. W., ed., Evolution of crop plants. Hybridization of haploids of potato in the plains London, 10-12, 1976. -
Hapaline Benthamiana Question Number Question Answer Score 1.01 Is the Species Highly Domesticated? N 0
Australia/New Zealand Weed Risk Assessment adapted for United States. Data used for analysis published in: Gordon, D.R. and C.A. Gantz. 2008. Potential impacts on the horticultural industry of screening new plants for invasiveness. Conservation Letters 1: 227-235. Available at: http://www3.interscience.wiley.com/cgi-bin/fulltext/121448369/PDFSTART Hapaline benthamiana Question number Question Answer Score 1.01 Is the species highly domesticated? n 0 1.02 Has the species become naturalised where grown? 1.03 Does the species have weedy races? 2.01 Species suited to U.S. climates (USDA hardiness zones; 0-low, 1- 2 intermediate, 2-high) 2.02 Quality of climate match data (0-low; 1-intermediate; 2-high) 2 2.03 Broad climate suitability (environmental versatility) n 0 2.04 Native or naturalized in regions with an average of 11-60 inches of annual y 1 precipitation 2.05 Does the species have a history of repeated introductions outside its ? natural range? 3.01 Naturalized beyond native range n -1 3.02 Garden/amenity/disturbance weed n 0 3.03 Weed of agriculture n 0 3.04 Environmental weed n 0 3.05 Congeneric weed n 0 4.01 Produces spines, thorns or burrs n 0 4.02 Allelopathic 4.03 Parasitic n 0 4.04 Unpalatable to grazing animals 4.05 Toxic to animals n 0 4.06 Host for recognised pests and pathogens 4.07 Causes allergies or is otherwise toxic to humans n 0 4.08 Creates a fire hazard in natural ecosystems 4.09 Is a shade tolerant plant at some stage of its life cycle 4.1 Grows on one or more of the following soil types: alfisols, entisols, or -
Atoll Research Bulletin No. 503 the Vascular Plants Of
ATOLL RESEARCH BULLETIN NO. 503 THE VASCULAR PLANTS OF MAJURO ATOLL, REPUBLIC OF THE MARSHALL ISLANDS BY NANCY VANDER VELDE ISSUED BY NATIONAL MUSEUM OF NATURAL HISTORY SMITHSONIAN INSTITUTION WASHINGTON, D.C., U.S.A. AUGUST 2003 Uliga Figure 1. Majuro Atoll THE VASCULAR PLANTS OF MAJURO ATOLL, REPUBLIC OF THE MARSHALL ISLANDS ABSTRACT Majuro Atoll has been a center of activity for the Marshall Islands since 1944 and is now the major population center and port of entry for the country. Previous to the accompanying study, no thorough documentation has been made of the vascular plants of Majuro Atoll. There were only reports that were either part of much larger discussions on the entire Micronesian region or the Marshall Islands as a whole, and were of a very limited scope. Previous reports by Fosberg, Sachet & Oliver (1979, 1982, 1987) presented only 115 vascular plants on Majuro Atoll. In this study, 563 vascular plants have been recorded on Majuro. INTRODUCTION The accompanying report presents a complete flora of Majuro Atoll, which has never been done before. It includes a listing of all species, notation as to origin (i.e. indigenous, aboriginal introduction, recent introduction), as well as the original range of each. The major synonyms are also listed. For almost all, English common names are presented. Marshallese names are given, where these were found, and spelled according to the current spelling system, aside from limitations in diacritic markings. A brief notation of location is given for many of the species. The entire list of 563 plants is provided to give the people a means of gaining a better understanding of the nature of the plants of Majuro Atoll. -
An Electronic Checklist of the New World Chafers (Coleoptera: Scarabaeidae: Melolonthinae)
AN ELECTRONIC CHECKLIST OF THE NEW WORLD CHAFERS (COLEOPTERA: SCARABAEIDAE: MELOLONTHINAE) Version 3 ARTHUR V. EVANS Research Associate, Department of Entomology, National Museum of Natural History, Smithsonian Institution, Washington, DC; Department of Recent Invertebrates, Virginia Museum of Natural History, Martinsville, VA; Department of Biology, Virginia Commonwealth University, Richmond, VA; c/o1600 Nottoway Ave., Richmond, VA 23227, USA; [email protected] and ANDREW B. T. SMITH Canadian Museum of Nature, P.O. Box 3443, Station D, Ottawa, ON, K1P 6P4, Canada; [email protected] INTRODUCTION The following is a checklist of all Melolonthinae (Coleoptera: Scarabaeidae) found in the New World. It has been modified from Evans (2003), Evans and Smith (2005), and Smith and Evans (2005) and has been updated to 13 March 2009. Included in this checklist are all of the available names given for New World Melolonthinae (both valid and invalid). Tribes are listed in traditional order (pseudo-phylogenetically) with genera, species, and subspecies listed alphabetically within. Under each valid generic name the subgenera and synonymies are listed as are type species and, in some cases, citations for keys, checklists, and bibliographies. Listed under each valid species are synonymies, distributional data by country, and citations for new combinations and spellings. A complete bibliography is included in the “References” section of all papers mentioned in the checklist. The purpose of this checklist is to present accurate and complete information for all the names of Melolonthinae in the New World. The taxonomy herein is based on the current literature (even if we have unpublished data contradicting what has been published) and the nomenclature carefully follows the International Code of Zoological Nomenclature. -
The Geography of Diversification in Mutualistic Ants: a Gene's-Eye View Into the Neogene History of Sundaland Rain Forests
Molecular Ecology (2007) doi:10.1111/j.l365-294X.2007.03294.x The geography of diversification in mutualistic ants: a gene's-eye view into the Neogene history of Sundaland rain forests S.-P. QUEK,*S. J. DAVIES4**P. S. ASHTON,t§T. ITINOf and N. E. PIERCE* *Museum of Comparative Zoology and iOrganismic and Evolutionary Biology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA, \Centerfor Tropical Forest Science — Arnold Arboretum Asia Program, 22 Divinity Avenue, Cambridge, MA 02138, USA, %Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AB, UK, fShinshu University, Department of Biology, Faculty of Science, 3-1-1 Asahi, Matsumoto Nagano 390-8621, Japan Abstract We investigate the geographical and historical context of diversification in a complex of mutualistic Crematogaster ants living in Macaranga trees in the equatorial rain forests of Southeast Asia. Using mitochondrial DNA from 433 ant colonies collected from 32 locations spanning Borneo, Malaya and Sumatra, we infer branching relationships, patterns of genetic diversity and population history. We reconstruct a time frame for the ants' diver- sification and demographic expansions, and identify areas that might have been refugia or centres of diversification. Seventeen operational lineages are identified, most of which can be distinguished by host preference and geographical range. The ants first diversified 16-20 Ma, not long after the onset of the everwet forests in Sundaland, and achieved most of their taxonomic diversity during the Pliocene. Pleistocene demographic expansions are inferred for several of the younger lineages. Phylogenetic relationships suggest a Bornean cradle and major axis of diversification. Taxonomic diversity tends to be associated with mountain ranges; in Borneo, it is greatest in the Crocker Range of Sabah and concentrated also in other parts of the northern northwest coast. -
11Th Flora Malesina Symposium, Brunei Darussalm, 30 June 5 July 2019 1
11TH FLORA MALESINA SYMPOSIUM, BRUNEI DARUSSALM, 30 JUNE 5 JULY 2019 1 Welcome message The Universiti Brunei Darussalam is honoured to host the 11th International Flora Malesiana Symposium. On behalf of the organizing committee it is my pleasure to welcome you to Brunei Darussalam. The Flora Malesiana Symposium is a fantastic opportunity to engage in discussion and sharing information and experience in the field of taxonomy, ecology and conservation. This is the first time that a Flora Malesiana Symposium is organized in Brunei Darissalam and in the entire island of Borneo. At the center of the Malesian archipelago the island of Borneo magnifies the megadiversity of this region with its richness in plant and animal species. Moreover, the symposium will be an opportunity to inspire and engage the young generation of taxonomists, ecologists and conservationists who are attending it. They will be able to interact with senior researchers and get inspired with new ideas and develop further collaboration. In a phase of Biodiversity crisis, it is pivotal the understanding of plant diversity their ecology in order to have a tangible and successful result in the conservation action. I would like to thank the Vice Chancellor of UBD for supporting the symposium. In the last 6 months the organizing committee has worked very hard for making the symposium possible, to them goes my special thanks. I would like to extend my thanks to all the delegates and the keynote speakers who will make this event a memorable symposium. Dr Daniele Cicuzza Chairperson of the 11th International Flora Malesiana Symposium UBD, Brunei Darussalam 11TH FLORA MALESINA SYMPOSIUM, BRUNEI DARUSSALM, 30 JUNE 5 JULY 2019 2 Organizing Committee Adviser Media and publicity Dr. -
A New Website for Araceae Taxonomy On
148 AROIDEANA, Vol. 31 A New Website for Araceae Taxonomy on www.cate-araceae.org A. Haigh, L Lay, S. J. Mayo, L Reynolds, and M. Sellaro Royal Botanic Gardens Kew, Richmond, Surrey 1W9 3AE, U.K. [email protected]; [email protected]; [email protected]; reynoldslm8@ yahoo.com; [email protected] J. Bogner Augsburger Str. 43a D - 86368 Gersthofen, Germany [email protected] P. C. Boyce Lot 12, Hillsdale Jalan Puncak Borneo Kota Padawan Kuching 93250 Sarawak, Malaysia [email protected] Thomas B. Croat, Michael H. Grayum, R. Keating, and C. Kostelac Missouri Botanical Garden P.O. Box 299, St. Louis, MO 63166 [email protected]; [email protected]; Richard.keating@ mobot.org; [email protected] A. Hay National Herbarium of New South Wales Royal Botanic Gardens Mrs Macquaries Road Sydney, New South Wales 2000, Australia ajmhay@hotmaiLcom W. Hetterscheid Wageningen University Botanic Garden Generaa1 Foulkesweg 37 6703 BL Wageningen, Netherlands [email protected] M.Mora Department of Biological Sciences Box 870345 The University of Alabama Tuscaloosa, AL 35487-0345, U.S.A. [email protected] Wong Sin Yeng [email protected] A. HAIGH ET Ai., 2008 149 ABSTRACT visions that there is great potential to make traditional taxonomy a much more excit The development and current progress ing, collective and dynamic activity than of the Cate-Araceae website is described ever before. But one common discovery and its relation to the aroid community that most E-Taxonomy websites make early discussed in the context of rapidly devel on is that without an interested community, oping initiatives to migrate traditional ready to focus on the web-delivered descriptive taxonomy onto the internet (E information, it is difficult to create the Taxonomy).