Aiphanes Acaulis, a New Species from Colombia

Total Page:16

File Type:pdf, Size:1020Kb

Aiphanes Acaulis, a New Species from Colombia 20 PRINCIPES (VOL. 29 Principe., 29(1), 1985, pp. 20-22 Aiphanes acaulis, a New Species from Colombia GLORIA GALEANO-GARCES l AND RODRIGO BERNAL-GONZALEZ2 Recent explorations for palms in north­ morsely toothed at apex, the upper mar­ western Colombia have revealed several gin produced into a cauda to 4 cm long, novelties, one of which, an interesting the apical pinnae narrowly cuneate, stemless species of Aiphanes, is described obliquely truncate at apex, 1-3 nerved, here as new to science. all pinnae glabrous above, the midnerve armed with 1-3 slender, bicolor, to 2 cm Aiphanes acaulis Galeano & Bernal sp. long bristles, glabrous below or with very nov. (Fig. 1) short, purplish-black bristles scattered on surface and veins; basal pinnae 7-24.5 Palma solitaria acaulis. Pinnae utrinque cm long along the upper margin, 0.7-2.1 18-30 regulariter in eadem planitie inser­ cm wide, central pinnae 10.8-27 cm long, tae, lineares vel angustissime cuneatae. 1.7-2.5 cm wide, apical pinnae 6.5-15.5 Spadix simplex. Antherae subquadraticae. cm long, to 5.6 cm wide at apex. Inflo­ Pistillodium inerme. rescence spicate: prophyll 16-26 cm long, Solitary, acaulescent. Leaves 8-10: 7-11 mm wide, linear, unarmed adaxi­ sheath 11-16 cm long, 1 cm wide, fibrous, ally, densely covered abaxially with irreg­ densely covered abaxially with irregular, ular brown scales and with very short, dark brown scales and with purplish-brown, appressed, purplish-brown bristles; pedun­ less than 0.5 mm long bristles, usually cular bract 37.5-94 cm long, unarmed, with a few black, flat spines; petiole 12.5­ with scattered, appressed, short, brown 50 cm long, with an indumentum of scales hairs; peduncle 12-88 cm long, with scat­ and bristles like that of the sheath, rarely tered, very short, purplish-brown bristles; armed with spines; rachis 42-75 cm long, spike 15-31 cm long, densely covered adaxially ridged, densely covered with with very short brown bristles; flowers purplish-black, to 5 mm long bristles, and purple, sunken, the pistillate ones distrib­ occasionally with scattered, slender, bicol­ uted along the proximal half or so, each or, to 2 cm long bristles, abaxially with with two staminate flowers above, the dis­ scaly indumentum like that of the sheath tal half with male flowers only. Staminate and with inconspicuous, brown, flat, very flowers 1.5-2.5 mm diam., broader than short (ca. 0.2 mm) bristles; pinnae 18-30 high: sepals imbricate, cucullate, mem­ on each side, regularly inserted, horizon­ branaceous, glabrous; petals glabrous, tally arranged in one plane, linear or very connate for half their length, the lobes narrowly cuneate, I-nerved, plicate along ovate; anthers nearly square, pistillode secondary veins, truncate and prae- minute, 3-gibbous. Pistillate flowers slightly larger: sepals broadly imbricate, glabrous; petals valvate, glabrous; gynoecium ovoid, 1 Apartado 51638, Medellin, Colombia. minutely verruculose, without bristles or 2 Departamento de Recursos Forestales, Facultad de Agronomia, Universidad Nacional de Colombia, spines; staminodial tube toothed. Fruit Apartado 568, Medellin, Colombia. unknown. 22 PRINCIPES [VOL. 29 Specimens examined: COLOMBIA, simplex Burret has clustered stems 2-4 DEPARTAMENTO DEL CHaCO: Muni­ m high, and its leaves bear 11-16 cuneate cipio de EI Carmen, vereda EI Doce (ca­ pinnae on each side; the other species, A. rretera Medellin-Quibdo, km 151), rio macroloba Burret, has leaves simple or Atrato, margen izquierda, 700 malt., with 3-4 pinnae on each side, and the enero 5, 1980, Bernal & Galeano 71 blade is beset above with very character­ (COL, holotype; HUA, K, isotypes), 72 istic long, soft bristles, scattered along the (COL, HUA); Municipio de Quibdo, Co­ vems. rregimiento de San Francisco de leho, rio Two further species, described with an Icho, margen derecha, 150 m alt., julio unbranched inflorescence, deserve a more 11, 1981, Galeano & Bernal 454 (COL, detailed discussion and will be the subject HUA, K). of another paper. These are A. chocoen­ Aiphanes acaulis is a very character­ sis A. Gentry and A. monostachys Bur­ istic species; it is readily distinguished from ret. The former has proved to be a syn­ the remaining species by the acaulescent onym of A. macroloba: comparison of the habit, the linear or very narrowly cuneate holotype of A. chocoensis with topotypes pinnae and the unbranched inflorescence. of A. macroloba leaves no doubt as to the In the habit and shape of pinnae it recalls identity of both species. A. monostachys, Aiphanes tessmannii Burret (1932), from on the other hand, was based on a mixed Peru, but the latter has an inflorescence collection, which included the inflores­ with many branches. cence of A. macroloba, as we will prove This species appears to be very uncom­ elsewhere. Both species were described mon, and only two small populations have from the same locality and both have been been located in the cited regions, although rediscovered there. The true A. mono­ several areas of northwestern Colombia stachys has an inflorescence with 15-28 have been explored in search of palms. rachillae. An emended description of A. Although some variation exists between monostachys will be provided in the forth­ both known populations, particularly in size coming paper. of leaves and inflorescence, there is no doubt that they are conspecific. LITERATURE CITED Besides A. acaulis, only two species BURRET, M. 1932. Die Palmengattungen Marti­ have a spicate inflorescence; both of them nezia und Aiphanes. Notizbl. Bot. Gart. Berlin are known only from Colombia. Aiphanes ll: 557-577..
Recommended publications
  • Aiphanes Grandis Borchs
    Palm Conservation – Palm Specialist Group Aiphanes grandis Borchs. & Balslev Status: Endangered (EN) Common name None recorded Natural range Aiphanes grandis is endemic to the western slopes of the Andes mountains in Ecuador, at elevations between 1000 and 2000 m. It occurs in cloud forest in the central and southern parts of the country. Recognition characteristics It is a large, solitary palm tree, with a stem up to 20 m tall and 10–20 cm in diameter. The stem and leaves are fiercely armed with long, black spines. The leaf blade is 200–250 cm long with up to 50 leaflets on each side, briefly jagged at apex, inserted in groups and pointing in different directions. The inflorescence is 1–1.5 m long, with up to 200 spreading branches. Flowers are white to pale yellow and fruits 2–3 cm in diameter, dull green and covered with brown, loosely attached bristles. The combination of jagged leaflets and large size distinguishes the species from all other South American palms. Natural history Little is known about the natural history of the species. The palm heart is edible, and its seeds are sometimes pureed and cooked with crude cane sugar to form a nougat-like paste. Threats to survival The estimated loss of potential habitat for A. grandis, based on habitat modeling, is 62%, most of which has occurred over the last 30–40 years. The west Andean mountain forest in southern and central Ecudor, where A. grandis occurs, harbors a high number of endemic plant species. It is also the home to remnant populations of such conspicuous palm species as Ceroxylon ventricosum and C.
    [Show full text]
  • Monocotyledons and Gymnosperms of Puerto Rico and the Virgin Islands
    SMITHSONIAN INSTITUTION Contributions from the United States National Herbarium Volume 52: 1-415 Monocotyledons and Gymnosperms of Puerto Rico and the Virgin Islands Editors Pedro Acevedo-Rodríguez and Mark T. Strong Department of Botany National Museum of Natural History Washington, DC 2005 ABSTRACT Acevedo-Rodríguez, Pedro and Mark T. Strong. Monocots and Gymnosperms of Puerto Rico and the Virgin Islands. Contributions from the United States National Herbarium, volume 52: 415 pages (including 65 figures). The present treatment constitutes an updated revision for the monocotyledon and gymnosperm flora (excluding Orchidaceae and Poaceae) for the biogeographical region of Puerto Rico (including all islets and islands) and the Virgin Islands. With this contribution, we fill the last major gap in the flora of this region, since the dicotyledons have been previously revised. This volume recognizes 33 families, 118 genera, and 349 species of Monocots (excluding the Orchidaceae and Poaceae) and three families, three genera, and six species of gymnosperms. The Poaceae with an estimated 89 genera and 265 species, will be published in a separate volume at a later date. When Ackerman’s (1995) treatment of orchids (65 genera and 145 species) and the Poaceae are added to our account of monocots, the new total rises to 35 families, 272 genera and 759 species. The differences in number from Britton’s and Wilson’s (1926) treatment is attributed to changes in families, generic and species concepts, recent introductions, naturalization of introduced species and cultivars, exclusion of cultivated plants, misdeterminations, and discoveries of new taxa or new distributional records during the last seven decades.
    [Show full text]
  • Ornamental Garden Plants of the Guianas, Part 3
    ; Fig. 170. Solandra longiflora (Solanaceae). 7. Solanum Linnaeus Annual or perennial, armed or unarmed herbs, shrubs, vines or trees. Leaves alternate, simple or compound, sessile or petiolate. Inflorescence an axillary, extra-axillary or terminal raceme, cyme, corymb or panicle. Flowers regular, or sometimes irregular; calyx (4-) 5 (-10)- toothed; corolla rotate, 5 (-6)-lobed. Stamens 5, exserted; anthers united over the style, dehiscing by 2 apical pores. Fruit a 2-celled berry; seeds numerous, reniform. Key to Species 1. Trees or shrubs; stems armed with spines; leaves simple or lobed, not pinnately compound; inflorescence a raceme 1. S. macranthum 1. Vines; stems unarmed; leaves pinnately compound; inflorescence a panicle 2. S. seaforthianum 1. Solanum macranthum Dunal, Solanorum Generumque Affinium Synopsis 43 (1816). AARDAPPELBOOM (Surinam); POTATO TREE. Shrub or tree to 9 m; stems and leaves spiny, pubescent. Leaves simple, toothed or up to 10-lobed, to 40 cm. Inflorescence a 7- to 12-flowered raceme. Corolla 5- or 6-lobed, bluish-purple, to 6.3 cm wide. Range: Brazil. Grown as an ornamental in Surinam (Ostendorf, 1962). 2. Solanum seaforthianum Andrews, Botanists Repository 8(104): t.504 (1808). POTATO CREEPER. Vine to 6 m, with petiole-tendrils; stems and leaves unarmed, glabrous. Leaves pinnately compound with 3-9 leaflets, to 20 cm. Inflorescence a many- flowered panicle. Corolla 5-lobed, blue, purple or pinkish, to 5 cm wide. Range:South America. Grown as an ornamental in Surinam (Ostendorf, 1962). Sterculiaceae Monoecious, dioecious or polygamous trees and shrubs. Leaves alternate, simple to palmately compound, petiolate. Inflorescence an axillary panicle, raceme, cyme or thyrse.
    [Show full text]
  • A Review of Animal-Mediated Seed Dispersal of Palms
    Selbyana 11: 6-21 A REVIEW OF ANIMAL-MEDIATED SEED DISPERSAL OF PALMS SCOTT ZoNA Rancho Santa Ana Botanic Garden, 1500 North College Avenue, Claremont, California 91711 ANDREW HENDERSON New York Botanical Garden, Bronx, New York 10458 ABSTRACT. Zoochory is a common mode of dispersal in the Arecaceae (palmae), although little is known about how dispersal has influenced the distributions of most palms. A survey of the literature reveals that many kinds of animals feed on palm fruits and disperse palm seeds. These animals include birds, bats, non-flying mammals, reptiles, insects, and fish. Many morphological features of palm infructescences and fruits (e.g., size, accessibility, bony endocarp) have an influence on the animals which exploit palms, although the nature of this influence is poorly understood. Both obligate and opportunistic frugivores are capable of dispersing seeds. There is little evidence for obligate plant-animaI mutualisms in palm seed dispersal ecology. In spite of a considerable body ofliterature on interactions, an overview is presented here ofthe seed dispersal (Guppy, 1906; Ridley, 1930; van diverse assemblages of animals which feed on der Pijl, 1982), the specifics ofzoochory (animal­ palm fruits along with a brief examination of the mediated seed dispersal) in regard to the palm role fruit and/or infructescence morphology may family have been largely ignored (Uhl & Drans­ play in dispersal and subsequent distributions. field, 1987). Only Beccari (1877) addressed palm seed dispersal specifically; he concluded that few METHODS animals eat palm fruits although the fruits appear adapted to seed dispersal by animals. Dransfield Data for fruit consumption and seed dispersal (198lb) has concluded that palms, in general, were taken from personal observations and the have a low dispersal ability, while Janzen and literature, much of it not primarily concerned Martin (1982) have considered some palms to with palm seed dispersal.
    [Show full text]
  • THE LESSER ANTILLES: Aboard the Sea Cloud
    THE LESSER ANTILLES: Aboard the Sea Cloud FEBRUARY 10-18, 2016 Red-necked Parrot, Amazona arausiaca LEADERS: VICTOR EMANUEL, BARRY LYON, DAVID ASCANIO, PETER ZIKA & JOHN HARRISON COMPILED BY: DAVID ASCANIO VICTOR EMANUEL NATURE TOURS, INC. 2525 WALLINGWOOD DRIVE, SUITE 1003 AUSTIN, TEXAS 78746 WWW.VENTBIRD.COM THE LESSER ANTILLES ABOARD THE SEA CLOUD FEBRUARY 10-18, 2016 By David Ascanio Once again, a sea with pastel blue or green colors, an incredible and rich history, outstanding cuisine, and the beautiful and breathtaking Sea Cloud, combined with exquisite birds resulted in a memorable journey across six of the Lesser Antilles to see all of the endemic parrots, tremblers, hummingbirds, orioles, and bullfinches that these islands offer. Our treasure wasn’t gold, nor sugar. It was every one of the endemic or the restricted distribution birds. It seemed as if every island offered a unique challenge to finding these treasures. Barbados was the easy task. In Dominica and Martinique we practiced patience. In Guadeloupe we built a successful group dynamic, while St. Lucia and St. Vincent challenged us with trails. Each day offered a unique experience, as if each of the Lesser Antilles had a distinctive personality. We started in British-flavored Barbados. A visit to the Graeme Hall Reserve allowed views of one of the few populations of Little Egret in the Americas. We also saw our first target species, the Barbados Bullfinch, one that’s so common that you can see it wandering around the swimming pool area of the hotel. After a full day sailing north, we made it to Dominica.
    [Show full text]
  • Notes on the Pollination Ecology of the Palm Genus Johannesteijsmannia (A Recaceae )
    Journal of Pollination Ecology, 6(15), 2011, pp 108-117 — Short Communication — NOTES ON THE POLLINATION ECOLOGY OF THE PALM GENUS JOHANNESTEIJSMANNIA (A RECACEAE ) Y.M. Chan* and L.G. Saw Forest Biodiversity Division, Forest Research Institute Malaysia, 52109 Kepong, Selangor, Malaysia Abstract The floral biology and flower visitors of the tropical palms Johannesteijsmannia altifrons, J. magnifica and J. perakensis were investigated. We combined the data from this study with published data of J. lanceolata to give an overview of the reproductive biology and pollination system of the genus. Anthesis peaks from 0500–1100 hrs when the inflorescences are visited mainly by flies, beetles and stingless bees ( Trigona ), the last are potential pollinators. The breeding system is facultative selfing, indicating the ability of the species to reproduce in the absence of pollinators or in isolation. Keywords: reproductive biology, pollinator, breeding system, flower biology, Coryphoideae, Johannesteijsmannia INTRODUCTION The reproductive biology of J. lanceolata has been well- documented (Chan et al. 2011b): It is self-compatible, the Studies on reproductive biology and pollination ecology flowers are homogamous with diurnal anthesis and are can help to shed light on plant-pollinator relationships, visited by bees, flies and ants. For the remaining members of evolution, and also possible reasons for the persistence, the genus, such information is lacking. Thus, we extended rarity, genetic diversity or species richness of plants (e.g. the investigations into the floral biology and pollination of J. Bawa et al. 1985; Henderson 2002; Rymer et al. 2005; altifrons , J. magnifica and J. perakensis , to determine the Barfod et al. 2011).
    [Show full text]
  • Perennial Edible Fruits of the Tropics: an and Taxonomists Throughout the World Who Have Left Inventory
    United States Department of Agriculture Perennial Edible Fruits Agricultural Research Service of the Tropics Agriculture Handbook No. 642 An Inventory t Abstract Acknowledgments Martin, Franklin W., Carl W. Cannpbell, Ruth M. Puberté. We owe first thanks to the botanists, horticulturists 1987 Perennial Edible Fruits of the Tropics: An and taxonomists throughout the world who have left Inventory. U.S. Department of Agriculture, written records of the fruits they encountered. Agriculture Handbook No. 642, 252 p., illus. Second, we thank Richard A. Hamilton, who read and The edible fruits of the Tropics are nnany in number, criticized the major part of the manuscript. His help varied in form, and irregular in distribution. They can be was invaluable. categorized as major or minor. Only about 300 Tropical fruits can be considered great. These are outstanding We also thank the many individuals who read, criti- in one or more of the following: Size, beauty, flavor, and cized, or contributed to various parts of the book. In nutritional value. In contrast are the more than 3,000 alphabetical order, they are Susan Abraham (Indian fruits that can be considered minor, limited severely by fruits), Herbert Barrett (citrus fruits), Jose Calzada one or more defects, such as very small size, poor taste Benza (fruits of Peru), Clarkson (South African fruits), or appeal, limited adaptability, or limited distribution. William 0. Cooper (citrus fruits), Derek Cormack The major fruits are not all well known. Some excellent (arrangements for review in Africa), Milton de Albu- fruits which rival the commercialized greatest are still querque (Brazilian fruits), Enriquito D.
    [Show full text]
  • Covers an Estimated Sixty Reside on the Island’S North-East Coast, Where Percent of the 289.8 Sq
    Palms Journal of the International Palm Society Vol. 53(2) Jun. 2009 THE INTERNATIONAL PALM SOCIETY, INC. The International Palm Society Palms (formerly PRINCIPES) Journal of The International Palm Society Founder: Dent Smith An illustrated, peer-reviewed quarterly devoted to The International Palm Society is a nonprofit corporation information about palms and published in March, engaged in the study of palms. The society is inter- June, September and December by The International national in scope with worldwide membership, and the Palm Society, 810 East 10th St., P.O. Box 1897, formation of regional or local chapters affiliated with the Lawrence, Kansas 66044-8897, USA. international society is encouraged. Please address all inquiries regarding membership or information about Editors: John Dransfield, Herbarium, Royal Botanic the society to The International Palm Society Inc., 6913 Gardens, Kew, Richmond, Surrey, TW9 3AE, United Poncha Pass, Austin, TX 78749-4371 USA. e-mail Kingdom, e-mail [email protected], tel. 44- [email protected], fax 512-607-6468. 20-8332-5225, Fax 44-20-8332-5278. Scott Zona, Dept. of Biological Sciences, Florida OFFICERS: International University (OE 167), 11200 SW 8 St., President: Bo-Göran Lundkvist, P.O. Box 2071, Pahoa, Miami, Florida 33199 USA, e-mail [email protected], tel. Hawaii 96778 USA, e-mail 1-305-348-1247, Fax 1-305-348-1986. [email protected], tel. 1-808-965-0081. Associate Editor: Natalie Uhl, 228 Plant Science, Vice-Presidents: John DeMott, 18455 SW 264 St, Cornell University, Ithaca, New York 14853 USA, e- Homestead, Florida 33031 USA, e-mail mail [email protected], tel.
    [Show full text]
  • A Tool Kit for Media in the OECS
    Keeping Biodiversity Issues in the News A Tool Kit for Media in the OECS Keeping Biodiversity in the News: A Tool Kit for Media in the OECS Keeping Biodiversity Issues in the News A Tool Kit for Media in the OECS Keeping Biodiversity in the News: A Tool Kit for Media in the OECS Cover Photo Credits: Peter Espeut, Greg Pereira and Tecla Fontenard Copyright © 2011 Organisation of Eastern Caribbean States Published by the Organisation of Eastern Caribbean States (OECS) Environment and Sustainable Development Unit (ESDU) The OECS Secretariat Morne Fortune P.O. Box 179 Castries Saint Lucia Telephone: (754) 452 2537 Fax: (754) 453 1628 Email: [email protected] Website: www.oecs.org All rights reserved. No part of this publication may be reproduced, stored in a retrieval system or transmitted in any form or by any means, electronic, mechanical, recording or otherwise, without prior permission of the Organisation of Eastern Caribbean States (OECS). Keeping Biodiversity in the News: A Tool Kit for Media in the OECS i FOREWARD By Keith Nichols Head of the Environmental Sustainable Development Unit (ESDU) Organisation of Eastern Caribbean States (OECS) ` Few people in the Caribbean region are aware that we live in one of the world’s most important “biodiversity hot spots”. The entire Caribbean region is recognized as the world’s fifth most critical bio- diversity hot spot – which means that many of the unique plants and animals that exist only in our region – and no where else – are under serious threat of extinction unless strong action is taken to protect them now.
    [Show full text]
  • Phylogenetic Relationships of the Cultivated Neotropical Palm Bactris
    SyltrmRtic 80lRny (2007), 32(3): pp, 519-530 l' Copyright2007 by the American Society of PlantTaxonomists Phylogenetic Relationships of the Cultivated Neotropical Palm Bactris gasipaes (Arecaceae) with its Wild Relatives Inferred from Chloroplast and Nuclear DNA Polymorphisms T. L. P. COUVREUR/·6 W. J. HAHN,2 J.-J. DE GRANVILLE/ J.-L. PHAM/ B. LUDENA,4 and 1A 5 I.-C PINTAUD • 1Institut de Recherche pour le Developpement (IRD), UMR DGPC/DYNADIV, 911 Avenue Agropolis BP 64501, 34394 Montpellier cedex 5, France; 20ffice of the Dean, Georgetown College and Dept. of Biology, Georgetown University, 37th & 0 Sts.. NW, Washington, DC 20057-1003, USA.; 3Herbarium CAY, Institut de Recherche pour le Developpement (IRD), B.P. 165, 97323 Cayenne Cedex, France; 4Pontificia Universidad Cat6lica del Ecuador, Laboratorio de Biologia Molecular de Eucariotes, Av. 12 de Octubre y Roca, Quite, Ecuador 5Present address: Institut de Recherche pour le Developpernent, Whimper 442 y Corufia, A.P. 17-12-857, Quito, Ecuador 6Author for correspondence, present address: Nationaal Herbarium Nederland (NHN), Wageningen University, Generaal Foulkesweg 37, 6703 BL Wageningen, The Netherlands ([email protected]) Communicating Editor: Gregory M. Plunkett ABSTRACf. Peach palm (Bactris gasipaes Kunth.) is the only Neotropical palm domesticated since pre-Columbian times. It plays an important role not only at the local level due to its very nutritious fruits, but also in the international market for its gourmet palm heart. Phylogenetic relationships of the peach palm with wild Bactris taxa are still in doubt, and have never been addressed using molecular sequence data. We generated a chloroplast DNA phylogeny using intergenic spacers from a sampling of cultivars of Bactris gasipaes as well as putative wild relatives and other members of the genus Baciris.
    [Show full text]
  • Multiplicity in Palm Uses by the Huaorani of Amazonian Ecuador
    Blackwell Science, LtdOxford, UKBOJBotanical Journal of the Linnean Society0024-4074The Linnean Society of London, 2003? 2003 1442 149159 Original Article PALM USES OF AMAZONIAN ECUADOR M. J. MACÍA Botanical Journal of the Linnean Society, 2004, 144, 149–159. With 1 figure Multiplicity in palm uses by the Huaorani of Amazonian Ecuador MANUEL J. MACÍA* Real Jardín Botánico de Madrid (CSIC), Plaza de Murillo 2, E-28014 Madrid, Spain Received March 2003; accepted for publication August 2003 An ethnobotanical study of the palms used by the Huaorani in the Yasuní National Park and Huaorani Ethnic Reserve in Amazonian Ecuador was carried out. In this inventory, 37 palm species were found; all were used by the Huaoranis. One hundred and ninety-one different uses were recorded in eight ethnobotanical categories. Most spe- cies (64.9%) were used for house construction and human food. More than half of the species were used for domestic utensils (59.4%) and hunting and fishing implements (54%). A comparison is made between these data and past stud- ies for the other six indigenous communities from Amazonian Ecuador. This paper shows the highest diversity of use- ful palm species and the highest number of different uses ever recorded for an indigenous group in Amazonian Ecuador. The data combine quantitative and qualitative approaches. © 2004 The Linnean Society of London, Botan- ical Journal of the Linnean Society, 2004, 144, 149–159. ADDITIONAL KEYWORDS: Arecaceae – ethnobotany – indigenous knowledge – non-timber forest products – Palmae – tropical rainforest. INTRODUCTION the biology of the tropical rainforest, and they use more than 1000 vascular plants for a variety of pur- Palms are the most useful plants for the rural and poses (Davis & Yost, 1983a; Cerón & Montalvo, 1998; indigenous people in Amazonia (e.g.
    [Show full text]
  • Coconut Rhinoceros Beetle, Oryctes Rhinoceros
    Coconut Rhinoceros Beetle, Oryctes rhinoceros A Major Threat to Hawaii’s Coconut and Palm Trees Aubrey Moore UG Crop Production Services Seminar & Tradeshow May 23, 2014 Topics to Be Covered *Coconut Rhinoceros Beetle -Known serious threat to Hawaii because of a severe CRB infestation in Guam since 2007 -Discovery in Hawaii in Dec 2013 -Attempt to eradicate the infestation +Control strategies =Physical Control (tub grinding infested mulch, bird netting) =Chemical (pyrethroids and neonicotinoids) =Heat (steam and hot water) =Composting (In-vessel - heat and ammonia toxicity) *”Oahu's Banyan Trees Are Under Attack, Many Are Dying” By Denby Fawcett 05/13/2014 CIVIL BEAT “Two major insects are attacking and killing Oahu’s banyan trees.” Lobate Lac Scale (Serious pest in Florida began 10 years ago) Ficus Stem Gall Wasp (new to science) LIFE CYCLE OF THE COCONUT RHINOCEROS BEETLE (CRB) Adult females lay eggs in dead Grubs (larvae) hatch in coconut palms, decaying organic 8 to 12 days from matter or mulch. whitish brown eggs (<1/4” long) laid in organic matter. Adults live 4 to 9 months; each Beetle feeding damage: female lays 50 to 140 eggs during hole bored into trunk her lifetime. (below); leaves with V- cuts (right) 1-1/4 to 2-1/4” long Grubs feed on decomposed Adult beetles remain in pupae for organic matter for 82 to 207 17- to 22 days, then emerge and days, and grow from ¼” to 4” fly to palm crowns to feed on long (3 instars). exududed sap. Egg to egg-laying adult 1-1/2 to 2” long (132 to 282 days) Grubs enter non-feeding prepupal stage for 8 to 13 days usually in the soil; pupal stage lasts 17 to 22 days.
    [Show full text]