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Notes on Oenocarpus (Palmae) in the Cowmbian Amazon
Bri/tonio. 43(3), 1991 . pp. 154-164 © 1991 , by the New York Botanical Garden, Bronx, NY 10458-5126 NOTES ON OENOCARPUS (PALMAE) IN THE COWMBIAN AMAZON RODRIGO G . BERNAL, GWRIA GALEANO, AND ANDREW HENDERSON Bernal, Rodrigo G., Gloria Galeano (Instituto de Ciencias Naturales, Univer sidad Nacional de Colombia, Apartado 7495, Bogota, Colombia) and Andrew Henderson (New York Botanical Garden, Bronx, NY 10458-5126). Notes on Oenocarpus (Palmae) in the Colombian Amazon. Brittonia 43: 154-164. 1991- Five species of Oenocarpus from the Rio Caquem. in the Colombian Amazon, are discussed. Two of them, Oenocarpus simplex and Oenocarpus makeru are described as new. Oenocarpus bacaba var. parvus is shown to be a synonym of O. balickii; this species and O. minor are recorded for the first time in Colombia. Some comments on the poorly known O. circumtextus are also given. The new findings support the inclusion of Jessenia in Oenocarpus. Se discuten cinco especies de Oenocarpus de la region del rio Caqueta, en la Amazonia Colombiana. Dos de elIas, Oenocarpus simplex y Oenocarpus makeru se describen como nuevas. Oenocarpus bacaba var. parvus es considerada un sin6nimo de O. balickii, y esta especie, junto con O. minor, es registrada por primera vez en Colombia. Se da infonnacion adicional sobre O. circumtextus, una especie muy poco conocida. Los nuevos hallazgos respaldan la union de Jessenia y Oenocarpus. Key words: Palmae, Oenocarpus, Jessenia, Colombian Amazon. Nine species were recognized by Balick (1986) in the most recent revision of the Jessenia-Oenocarpus complex. Two new varieties of Oenocarpus bacaba C. Martius from Venezuela were later added by Wessels Boer (1988), and a new species of Oenocarpus C. -
Oenocarpus Bataua Mart.): a Palm from the Amazon
International Journal of Plant & Soil Science 31(6): 1-7, 2019; Article no.IJPSS.54389 ISSN: 2320-7035 Mineralogical Composition and Bioactive Molecules in the Pulp and Seed of Patauá (Oenocarpus bataua Mart.): A Palm from the Amazon S. A. M. Saravia1*, I. F. Montero2, B. M. Linhares3, R. A. Santos4 and J. A. F. Marcia5 1Faculty of Earth Sciences and Conservation, National University of Agriculture, Highway to Dulce Nombre de Culmi, Km 215, Neighborhood El Espino, Catacamas-Olancho, Honduras. 2Department of Organic and Inorganic Chemistry, Polytechnic School, University of Extremadura, University Avenue s/n, Cáceres, Spain. 3Federal Institute of Roraima, Campus Boa Vista, Av. Glaycon de Paiva, 2496 - Pricumã, Boa Vista - RR, 69303-340, Brazil. 4Department of Food Science, Louisiana State University, USA. 5Faculty of Technological Sciences, National University of Agriculture, Highway to Dulce Nombre de Culmi, Km 215, Neighborhood El Espino, Catacamas-Olancho, Honduras. Authors’ contributions This work was carried out in collaboration among all authors. Author SAMS contributed to the analysis, literature review and formatting of the article. Author IFM contributed to the supervision of the analysis, writing of the article and review of language and style. Author BML contributed to the collection of the material, sample preparation and analysis. Authors RAS and JAFM contributed to the review, editing of the article, the verification, validation of the methods and analysis being used in the experiments. All authors read and approved the final manuscript. Article Information DOI: 10.9734/IJPSS/2019/v31i630228 Editor(s): (1) Dr. Olanrewaju Folusho Olotuah, Professor, Department of Plant Science and Biotechnology, Adekunle Ajasin University, Akungba-Akoko, Ondo State, Nigeria. -
Red Ring Disease of Coconut Palms Is Caused by the Red Ring Nematode (Bursaphelenchus Cocophilus), Though This Nematode May Also Be Known As the Coconut Palm Nematode
1 Red ring disease of coconut palms is caused by the red ring nematode (Bursaphelenchus cocophilus), though this nematode may also be known as the coconut palm nematode. This disease was first described on coconut palms in 1905 in Trinidad and the association between the disease and the nematode was reported in 1919. The vector of the nematode is the South American palm weevil (Rhynchophorus palmarum), both adults and larvae. The nematode parasitizes the weevil which then transmits the nematode as it moves from tree to tree. Though the weevil may visit many different tree species, the nematode only infects members of the Palmae family. The nematode and South American palm weevil have not yet been observed in Florida. 2 Information Sources: Brammer, A.S. and Crow, W.T. 2001. Red Ring Nematode, Bursaphelenchus cocophilus (Cobb) Baujard (Nematoda: Secernentea: Tylenchida: Aphelenchina: Aphelenchoidea: Bursaphelechina) formerly Rhadinaphelenchus cocophilus. University of Florida, IFAS Extension. EENY236. Accessed 11-27-13 http://edis.ifas.ufl.edu/in392 Griffith, R. 1987. “Red Ring Disease of Coconut Palm”. The American Pathological Society Plant Disease, Volume 71, February, 193-196. accessed 12/5/2013- http://www.apsnet.org/publications/plantdisease/ba ckissues/Documents/1987Articles/PlantDisease71n02_193.PDF Griffith, R., R. M. Giblin-Davis, P. K. Koshy, and V. K. Sosamma. 2005. Nematode parasites of coconut and other palms. M. Luc, R. A. Sikora, and J. Bridges (eds.) In Plant Parasitic Nematodes in Subtropical and Tropical Agriculture. C.A.B. International, Oxon, UK. Pp. 493-527. 2 The host trees susceptible to the red ring nematode are usually found in the family Palmae. -
Ethnobotany of Riverine Populations from the Rio Negro, Amazonia (Brazil)
Journal of Ethnobiology 27(1): 46–72 Spring/Summer 2007 ETHNOBOTANY OF RIVERINE POPULATIONS FROM THE RIO NEGRO, AMAZONIA (BRAZIL) ANDRE´ A LEME SILVA,a JORGE TAMASHIROb and ALPINA BEGOSSIc aDepartamento de Ecologia, Instituto de Biocieˆncias Universidade de Sa˜o Paulo, Sa˜o Paulo, Brazil, CEP 05580-900 ^[email protected]& bDepartamento de Botaˆnica, UNICAMP Campinas, Sa˜o Paulo, Brazil ^[email protected]& cFisheries and Food Institute, Rua Coronel Quirino 1636, Campinas, Sa˜o Paulo 13025-002, Brazil, and Fisheries Management and Training Program, PREAC-UNICAMP ^[email protected]& ABSTRACT.—This paper presents a comparative study of plant knowledge and use in rural and urban areas in the municipality of Barcelos in the Rio Negro, Amazonas, Brazil, based on a total of 81 interviews. Using diversity indices (Shannon-Wiener), plant knowledge is compared among communities (urban- rural population), and between sex (male-female) and age (older or younger than 40 years) categories within each community. Among our informants, we found quantitative differences concerning the knowledge of medicinal plants between sex and age categories. Some individuals play a key role relating to medicinal plant knowledge, and steps should be taken in order to include them in management and conservation plans. Key words: ethnobotany, diversity indices, plant knowledge and use, Rio Negro, Brazilian Amazon. RESUMO.—Com base em um total de 81 entrevistas, no´s apresentamos um estudo etnobotaˆnico comparativo entre populac¸o˜es urbanas e rurais na municipalidade de Barcelos no Rio Negro, Amazonas, Brasil. Usando´ ındices de diversidade (Shannon-Wiener), o conhecimento de plantas e´ comparado entre as comunidades estudadas (populac¸a˜o urbana e rural), geˆnero (masculino e feminino) e categorias de idade (menos que 40 anos e mais que 40 anos de idade). -
Restoring Tropical Forests on Lands Mined for Bauxite: Examples from the Brazilian Amazon
Ecological Engineering 17 (2001) 219–239 www.elsevier.com/locate/ecoleng Restoring tropical forests on lands mined for bauxite: Examples from the Brazilian Amazon John A. Parrotta a,*, Oliver H. Knowles b a International Institute of Tropical Forestry, USDA Forest Ser6ice, P.O. Box 25000, Rı´o Piedras, PR 00928-5000, USA b C.P. 15, Santare´m, 68005.970 Para´, Brazil Accepted 19 August 2000 Abstract Restoring self-sustaining tropical forest ecosystems on surface mined sites is a formidable challenge that requires the integration of proven reclamation techniques and reforestation strategies appropriate to specific site conditions, including landscape biodiversity patterns. Restorationists working in most tropical settings are usually hampered by lack of basic information on the wide variety of native tree species that characterize the pre-disturbance forests, as well as insufficient understanding of the ecology of disturbance and natural recovery to design effective restoration programs. A notable exception to this is the forest restoration program developed since the early 1980s by a Brazilian bauxite mining company operating at Trombetas in Para´ State in central Amazonia. A systematic nursery and field research strategy was used to develop a reforestation program based on mixed plantings of more than 70 native old-growth forest tree species. This technique has been used to replant about 100 ha of deforested minelands each year over the past 15 years. Research in recent years has evaluated this approach and other, generally simpler, reforestation methods used at a smaller scale at this site. Post-plantation biodiversity development and other indicators of restoration success or sustainability were recorded. -
Behavior and Ecology of the White-Footed Tamarin (Saguinus Leucopus) in a Fragmented Landscape of Colombia
Mongabay.com Open Access Journal - Tropical Conservation Science Vol. 9 (2): 788-808, 2016 Research Article Behavior and ecology of the white-footed tamarin (Saguinus leucopus) in a fragmented landscape of Colombia: small bodied primates and seed dispersal in Neotropical forests A. Gabriela de Luna1, 2,*, Yesenia García-Morera1, 3 and Andrés Link1, 4, 5 1Fundación Proyecto Primates 2Departamento de Zoología y Antropología, Facultad de Biología, Universidad Complutense, España 3Instituto de Biología, Universidad de Antioquia, Colombia 4Departamento de Ciencias Biológicas, Universidad de los Andes, Colombia 5Facultad de Administración, Universidad de los Andes, Colombia *Corresponding author. Email: [email protected] Abstract Tamarins are small-bodied Neotropical primates that mainly feed on ripe fruits and insects, and supplement their diet with plant exudates, nectar, fungi and vertebrate prey. They are important seed dispersers in Neotropical forests as they are able to disperse a large number of small and me- dium-sized seeds from parental trees. In this paper, we describe the diet of the white-footed tama- rin (Saguinus leucopus) and its role as seed disperser in a fragmented landscape in Colombia. During a twelve month period, we collected data on activity patterns, ranging behavior and feeding ecol- ogy, as well as on habitat-wide forest productivity. S. leucopus fed from >95 plant species and spent 17% of their time feeding. We found a positive relationship between fruit consumption and ripe- fruit availability. Dietary diversity increased during periods of fruit scarcity, when the tamarins fed more on insects and exudates. During periods of fruit scarcity, they relied more heavily on the bor- ders of forest fragments and made occasional incursions into adjacent fragments across a matrix of pastures. -
Genetic Diversity of Dispersed Seeds Is Highly Variable Among Leks of the T Long-Wattled Umbrellabird
Acta Oecologica 86 (2018) 31–37 Contents lists available at ScienceDirect Acta Oecologica journal homepage: www.elsevier.com/locate/actoec Genetic diversity of dispersed seeds is highly variable among leks of the T long-wattled umbrellabird ∗ Kym Ottewella,c, Luke Brownea,b,d, Domingo Cabrerab, Jorge Olivob, Jordan Karubiana,b, a Department of Ecology and Evolutionary Biology, Tulane University, 400 Lindy Boggs Building, New Orleans, LA 70118, USA b Fundación para la Conservación de los Andes Tropicales, Mariano Hurtado N 50-89 y Vicente Herida, Quito, Ecuador c Department of Biodiversity, Conservation and Attractions, 17 Dick Perry Avenue, Kensington, Western Australia 6158, Australia d UCLA La Kretz Center for California Conservation Science, Institute of the Environment and Sustainability, Los Angeles, CA 90095, USA ARTICLE INFO ABSTRACT Keywords: Frugivorous animals frequently generate clumped distributions of seeds away from source trees, but genetic Alpha, beta, delta and gamma diversity consequences of this phenomenon remain poorly resolved. Seed dispersal of the palm Oenocarpus bataua by long- Allelic diversity wattled umbrellabirds Cephalopterus penduliger generates high seed densities in leks (i.e., multi-male display fl Gene ow sites), providing a suitable venue to investigate how dispersal by this frugivore may influence seed source di- Heterozygosity versity and genetic structure at local and landscape levels. We found moderate levels of maternal seed source Central place foraging diversity in primary seed rain across five leks in northwest Ecuador (unweighted mean alpha diversity α = 9.52, Seed dispersal α α – Ecuador weighted mean r = 3.52), with considerable variation among leks ( r range: 1.81 24.55). -
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. -
Information Sheet on Ramsar Wetlands (RIS) – 2009-2012 Version Available for Download From
Information Sheet on Ramsar Wetlands (RIS) – 2009-2012 version Available for download from http://www.ramsar.org/ris/key_ris_index.htm. Categories approved by Recommendation 4.7 (1990), as amended by Resolution VIII.13 of the 8th Conference of the Contracting Parties (2002) and Resolutions IX.1 Annex B, IX.6, IX.21 and IX. 22 of the 9th Conference of the Contracting Parties (2005). Notes for compilers: 1. The RIS should be completed in accordance with the attached Explanatory Notes and Guidelines for completing the Information Sheet on Ramsar Wetlands. Compilers are strongly advised to read this guidance before filling in the RIS. 2. Further information and guidance in support of Ramsar site designations are provided in the Strategic Framework and guidelines for the future development of the List of Wetlands of International Importance (Ramsar Wise Use Handbook 14, 3rd edition). A 4th edition of the Handbook is in preparation and will be available in 2009. 3. Once completed, the RIS (and accompanying map(s)) should be submitted to the Ramsar Secretariat. Compilers should provide an electronic (MS Word) copy of the RIS and, where possible, digital copies of all maps. 1. Name and address of the compiler of this form: FOR OFFICE USE ONLY. DD MM YY Beatriz de Aquino Ribeiro - Bióloga - Analista Ambiental / [email protected], (95) Designation date Site Reference Number 99136-0940. Antonio Lisboa - Geógrafo - MSc. Biogeografia - Analista Ambiental / [email protected], (95) 99137-1192. Instituto Chico Mendes de Conservação da Biodiversidade - ICMBio Rua Alfredo Cruz, 283, Centro, Boa Vista -RR. CEP: 69.301-140 2. -
PHENOLOGY, BIOMETRICS and FRUITS PRODUCTION of Attalea
Facultad de Ciencias ACTA BIOLÓGICA COLOMBIANA Departamento de Biología http://www.revistas.unal.edu.co/index.php/actabiol Sede Bogotá ARTÍCULO DE INVESTIGACIÓN / RESEARCH ARTICLE BOTÁNICA PHENOLOGY, BIOMETRICS AND FRUITS PRODUCTION OF Attalea nucifera (ARECACEAE) IN COLOMBIA FENOLOGÍA, PARÁMETROS BIOMÉTRICOS Y PRODUCTIVIDAD DE FRUTOS DE Attalea nucifera (ARECACEAE) EN COLOMBIA Ivón Jiménez-Morera1 , Néstor García1 1Departamento de Biología, Facultad de Ciencias, Pontificia Universidad Javeriana, Carrera 7 No. 40 – 62, Bogotá, Colombia *For correspondence: [email protected] Received: 06th February 2019, Returned for revision: 03rd May 2019, Accepted: 28th May 2019. Associate Editor: Xavier Marquínez-Casas. Citation/Citar este artículo como: Jiménez-Morera I, García N. Phenology, biometrics and fruits production of Attalea nucifera (Arecaceae) in Colombia. Acta biol. Colomb. 2020;25(1):104-111. DOI: http://dx.doi.org/10.15446/abc.v25n1.77701 ABSTRACT Attalea nucifera is a threatened palm endemic to the Magdalena River basin in Colombia. In the past its seeds were consumed by the inhabitants of the town of Guaduas, Cundinamarca, although currently its use is less frequent. To assess the productive potential of this palm, we studied its phenology, biometric parameters, and fruit productivity in a forest relict in Guaduas. Field work was carried out between April 2016 and March 2017. The reproductive cycle of this species lasted approximately 12 and a half months from bud to fruit ripening. Although bud production occurred throughout the year, it increased during periods of greatest rainfall. Flowering peaks occurred towards the end of the rainy season and fruits ripened towards the period of low rainfall. We found a positive correlation between the number of leaves in the crown and the production of reproductive structures (rs = 0.447, p = 0.004). -
Rhynchophorus Palmarum
EPPO Datasheet: Rhynchophorus palmarum Last updated: 2020-09-02 IDENTITY Preferred name: Rhynchophorus palmarum Authority: (Linnaeus) Taxonomic position: Animalia: Arthropoda: Hexapoda: Insecta: Coleoptera: Dryophthoridae Other scientific names: Calandra palmarum (Linnaeus), Cordyle barbirostris Thunberg, Curculio palmarum Linnaeus, Rhynchophorus barbirostris (Thunberg), Rhynchophorus cycadis Erichson, Rhynchophorus depressus Chevrolet, Rhynchophorus languinosus Chevrolet Common names: South American palm weevil, giant palm weevil, more photos... palm marrow weevil, palm marrow weevil, palm weevil view more common names online... EPPO Categorization: A1 list view more categorizations online... EU Categorization: A1 Quarantine pest (Annex II A) EPPO Code: RHYCPA HOSTS R. palmarum has been reported on at least 35 plant species in at least 12 different families. However, it is primarily found in association with palms (Arecaceae) (Esser & Meredith, 1987; Grif?th, 1987; Wattanapongsiri, 1966; Jaffé & Sánchez, 1990; Sánchez & Cerda, 1993). With respect to palms, R. palmarum is commonly reported as a pest. It has also been observed reproducing on sugarcane stems, a non-palm host, (Arango & Rizo, 1977; Restrepo et al., 1982). Feeding damage by larvae to the apical meristematic region (i.e. the palm heart) causes palm mortality (Milosavljevi? et al., 2019). When reported on other plants, R. palmarum adults were observed feeding on ripe fruit. This type of feeding on fruit by adult weevils is typically not a source of significant economic damage. Breeding hosts: R. palmarum breeding is primarily restricted to palms (Arecaceae) and known hosts include: Brahea edulis (Guadalupe palm), Cocos nucifera (coconut), Dypsis lutescens (golden cane palm), Elaeis guineensis (African oil palm), Euterpe edulis (juçara, grown for hearts of palm), Livistona australis (cabbage tree palm), Metroxylon sagu (true sago palm), Phoenix canariensis (Canary Islands date palm), P. -
Oenocarpus Bataua
ISSN 0101-2061 Ciência e Tecnologia de Alimentos Original Nutritional composition, fatty acid and tocopherol contents of buriti (Mauritia flexuosa) and patawa (Oenocarpus bataua) fruit pulp from the Amazon region Composição centesimal, em ácidos graxos e tocoferóis das polpas amazônicas de buriti (Mauritia flexuosa) e de patauá (Oenocarpus bataua) Sylvain Henri DARNET1, Luiza Helena Meller da SILVA2*, Antonio Manoel da Cruz RODRIGUES2, Roseana Telles LINS2 Abstract Buriti and patawa are two endemic palm trees from the Amazon region. Their pulps are traditionally consumed by the local population, but are underused and lesser known worldwide. Nutritional composition, fatty acid and tocopherol contents of the two palm pulps were determined by modern analytical methods: Gas Chromatography (CG) and High Performance Liquid Chromatography (HPLC), based on the standards of AOCS (AMERICAN..., 2002) and AOAC (ASSOCIATION..., 1997), respectively. Buriti and patawa fruit pulps are highly nutritive, with respectively, high fat content (38.4% and 29.1% of dry matter (DM)), protein content (7.6% and 7.4% of DM) and dietary fibers (46% and 44.7% of DM). Buriti pulp can be considered healthy food due its high content of vitamin E (1169 µg.g–1 DM). Patawa pulp is highly oleaginous and its fatty acid composition is very similar to the ones of healthy oils, such as olive oil. Keywords: Amazon; pulp; fruit; palm; buriti; Mauritia flexuosa; patawa; Oenocarpus bataua; lipids; fatty acids; tocopherols. Resumo O buriti e o patauá são duas palmeiras endêmicas da região Amazônica. As polpas destes frutos são tradicionalmente consumidas pela população local, mas ainda não ganharam os mercados nacional e internacional.