Samara Newsletter July & August 2020
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Natural Resources Conservation Service Conservation General Specifications
NATURAL RESOURCES CONSERVATION SERVICE CONSERVATION GENERAL SPECIFICATIONS RIPARIAN FOREST BUFFER (Acre) Code 391 Procedures, technical details and other establishing new buffers. Ecological life information listed below provide additional zones, described by Ewel & Withmore, 1973, guidance for carrying out selected for Puerto Rico and the U. S. Virgin Islands components of the Riparian Forest Buffer. are major climatic divisions and define the This material is referenced from the conditions for ecosystem functioning (see conservation practice standard for the pages 5 and 6 for Ecological Life Zones map named practice and supplements the for Puerto Rico and U. S. Virgin Islands). requirements and considerations listed therein. Natural regeneration may be used to establish a buffer if the following conditions PLANTING DENSITIES exist: Initial plant-to-plant densities for trees and • There is an adequate natural seed shrubs will depend on their potential height source of desired species in adjacent at 20 years of age. Heights may be areas. estimated based on performance of the • Site conditions are favorable for individual species (or comparable species) establishing the desired number and in nearby areas on similar sites, or distribution of seedlings within specified technical references. Planting density time period. specifications are: • Noxious or invasive species are not likely to jeopardize the stand. Plant Plant-to-Plant CARE, HANDLING, SIZE AND PLANTING Types/Heights: Spacing (ft) REQUIREMENTS FOR WOODY PLANTING Shrubs 3 to 15 STOCK Trees 8 to 20 Planting stock will be stored in a cool, moist environment. During all stages of handling PLANT LIST and storage, keep stock tops dry and free of Table 1 includes the lists of woody plant mold and roots moist and cool. -
PC14 Inf. 11 (English Only/Únicamente En Inglés/Seulement En Anglais)
PC14 Inf. 11 (English only/Únicamente en inglés/Seulement en anglais) CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES OF WILD FAUNA AND FLORA ____________ Fourteenth meeting of the Plants Committee Windhoek (Namibia), 16-20 February 2004 COMPILATION OF COMMENTS REGARDING THE APPLICABILITY OF VARIOUS CRITERIA TO ASSESS THE STATUS OF FLORA FOR LISTING UNDER CITES APPENDIX II 1. This document has been prepared by the United States of America. Pseudophoenix ekmanii, Dominican cherry palm (palm): It seems that the guidance provided at the beginning of this table specifying that the “species must fulfill the trade criterion and at least one of the criteria A-D,” was included just for the purposes of this review. However, it could be modified General somewhat (see below) and retained. comments from reviewer on THE FOLLOWING EDITORIAL CHANGES ARE PROPOSED: “For your information for a species to fulfill the draft criteria for Appendix I it must meet the applicability of trade criteria criterion and at least one of the biological criteria, A-D.” criteria for listing on Appendix II GENERAL COMMENTS: For plants, issues such as seed bank viability and primary mode of sexual reproduction should be provided/requested at some point. Terms such as “generation length” (a.k.a generation time), “possibly extinct” and “threatened with extinction” are in the glossary but not mentioned in the text of the table. Should there be a more direct reference to them? PC14 Inf. 11 – p. 1 CRITERION COMMENTS AND SPECIES ASSESSMENETS Aloe ferox, Tap aalwyn (an aloe): Yes. ****************************************************************************************************************** Cibotium barometz (tree fern): Yes. Cibotium barometz is in trade as wild plants. -
Proceedings Amurga Co
PROCEEDINGS OF THE AMURGA INTERNATIONAL CONFERENCES ON ISLAND BIODIVERSITY 2011 PROCEEDINGS OF THE AMURGA INTERNATIONAL CONFERENCES ON ISLAND BIODIVERSITY 2011 Coordination: Juli Caujapé-Castells Funded and edited by: Fundación Canaria Amurga Maspalomas Colaboration: Faro Media Cover design & layout: Estudio Creativo Javier Ojeda © Fundación Canaria Amurga Maspalomas Gran Canaria, December 2013 ISBN: 978-84-616-7394-0 How to cite this volume: Caujapé-Castells J, Nieto Feliner G, Fernández Palacios JM (eds.) (2013) Proceedings of the Amurga international conferences on island biodiversity 2011. Fundación Canaria Amurga-Maspalomas, Las Palmas de Gran Canaria, Spain. All rights reserved. Any unauthorized reprint or use of this material is prohibited. No part of this book may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, or by any information storage and retrieval system without express written permission from the author / publisher. SCIENTIFIC EDITORS Juli Caujapé-Castells Jardín Botánico Canario “Viera y Clavijo” - Unidad Asociada CSIC Consejería de Medio Ambiente y Emergencias, Cabildo de Gran Canaria Gonzalo Nieto Feliner Real Jardín Botánico de Madrid-CSIC José María Fernández Palacios Universidad de La Laguna SCIENTIFIC COMMITTEE Juli Caujapé-Castells, Gonzalo Nieto Feliner, David Bramwell, Águedo Marrero Rodríguez, Julia Pérez de Paz, Bernardo Navarro-Valdivielso, Ruth Jaén-Molina, Rosa Febles Hernández, Pablo Vargas. Isabel Sanmartín. ORGANIZING COMMITTEE Pedro -
Baobab (Not Boabab) Species General Background Germinating
Baobab (not Boabab) Species Baobab is the common name of a genus (Adansonia) with eightspecies of trees, 6 species in Madagascar; 1 in Africa and 1 in Australia. Adansonia gregorii (A.gibbosa) or Australian Baobab (northwest Australia) Adansonia madaf Zascariensis or Madagascar Baobab (Madagascar) Adansonia perrieri or Perrier's Baobab (North Madagascar) Adansonia rubrostipa or Fony Baobab (Madagascar) Adansonia suarezensis or Suarez Baobab Diego Suarez,(Madagascar) Adansonia za or Za Baobab (Madagascar) The name Adansonia honours Michel Adanson, the French naturalist and explorer who described A. digitata. General Background One of the earliest written references to the Baobab tree was made by the Arabic traveller, Al-Bakari in 1068. In 1592, the Venetian herbalist and physician, Prospero Alpino, reported a fruit in the markets of Cairo as "BU HUBAB". It is believed that the name is derived from the Arabic word Bu Hibab which means fruit with many seeds. Common names include bottle tree and monkey bread tree. Baobab - derived from African fokelore "upside-down-tree". The story is after the creation each of the animals were given a tree to plant and the stupid hyena planted the baobab upside-down. The baobab is the national tree of Madagascar. Height is 5-25m tall and trunk diameter of up to 7m. The Baobab can store up to 120 000 lt of water inside the swollen trunk to endure harsh drought conditions. All occur in seasonal arid areas and are deciduous, losing leaves during dry season. It is believed that the elephant must digest the seed before it will germinate as the heat and stomach acids help to soften the shell. -
Fruits: Kinds and Terms
FRUITS: KINDS AND TERMS THE IMPORTANT PART OF THE LIFE CYCLE OFTEN IGNORED Technically, fruits are the mature ovaries of plants that contain ripe seeds ready for dispersal • Of the many kinds of fruits, there are three basic categories: • Dehiscent fruits that split open to shed their seeds, • Indehiscent dry fruits that retain their seeds and are often dispersed as though they were the seed, and • Indehiscent fleshy fruits that turn color and entice animals to eat them, meanwhile allowing the undigested seeds to pass from the animal’s gut We’ll start with dehiscent fruits. The most basic kind, the follicle, contains a single chamber and opens by one lengthwise slit. The columbine seed pods, three per flower, are follicles A mature columbine follicle Milkweed seed pods are also large follicles. Here the follicle hasn’t yet opened. Here is the milkweed follicle opened The legume is a similar seed pod except it opens by two longitudinal slits, one on either side of the fruit. Here you see seeds displayed from a typical legume. Legumes are only found in the pea family Fabaceae. On this fairy duster legume, you can see the two borders that will later split open. Redbud legumes are colorful before they dry and open Lupine legumes twist as they open, projecting the seeds away from the parent The bur clover modifies its legumes by coiling them and providing them with hooked barbs, only opening later as they dry out. The rattlepods or astragaluses modify their legumes by inflating them for wind dispersal, later opening to shed their seeds. -
Eocene Fossil Legume Leaves Referable to the Extant Genus Arcoa (Caesalpinioideae, Leguminosae)
Int. J. Plant Sci. 180(3):220–231. 2019. q 2019 by The University of Chicago. All rights reserved. This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0), which permits non-commercial reuse of the work with at- tribution. For commercial use, contact [email protected]. 1058-5893/2019/18003-0005$15.00 DOI: 10.1086/701468 EOCENE FOSSIL LEGUME LEAVES REFERABLE TO THE EXTANT GENUS ARCOA (CAESALPINIOIDEAE, LEGUMINOSAE) Patrick S. Herendeen1,* and Fabiany Herrera* *Chicago Botanic Garden, 1000 Lake Cook Road, Glencoe, Illinois 60022, USA Editor: Michael T. Dunn Premise of research. Fossil leaves from the early Eocene Green River Formation of Wyoming and late Eo- cene Florissant Formation of Colorado have been studied and described here as two species in the monospe- cific extant genus Arcoa (Leguminosae, subfamily Caesalpinioideae). The single living species of Arcoa is en- demic to the Caribbean island of Hispaniola. The species from Florissant has been known since the late 1800s but has been incorrectly treated as several different legume genera. Methodology. The compression fossils were studied using standard methods of specimen preparation and microscopy. Fossils were compared with extant taxa using herbarium collections at the Field Museum and Smithsonian Institution. Pivotal results. The fossil bipinnate leaves exhibit an unusual morphological feature of the primary rachis, which terminates in a triad of pinnae, one terminal flanked by two lateral pinnae, all of which arise from the same point at the apex of the rachis. This feature, combined with other features that are diagnostic of the family Leguminosae or subgroups within it, allows the taxonomic affinities of the fossil leaves to be definitively deter- mined as representing the extant genus Arcoa, which is restricted to the Caribbean island of Hispaniola today. -
Caribbean Ornithology
The Journal of Caribbean Ornithology RESEARCH ARTICLE Vol. 29:21–27. 2016 Avian biodiversity in a pasture-dominated ecosystem Jason P. Hernandez Photo: J.P. Hernandez The Journal of Caribbean Ornithology www.birdscaribbean.org/jco ISSN 1544-4953 RESEARCH ARTICLE Vol. 29:21–27. 2016 www.birdscaribbean.org Avian biodiversity in a pasture-dominated ecosystem Jason P. Hernandez Abstract Burgeoning human populations have created many challenges for conservation of biodiversity, as ever-larger areas of land are converted to agricultural and other forms of production. Protected reserves alone are not sufficient to sustain biodiversity in a world of increasing human needs, so it is necessary to understand the extent to which biodiversity can exist with- in highly altered, agricultural ecosystems. From 11 May to 8 August 2013, bird diversity was surveyed at an agricultural site on Hispaniola, utilized mainly for pasture, and the population and regeneration potential of the royal palm (Roystonea borinquena), a key nest tree species for two abundant bird species, was assessed. The site harbored 33 bird species including 32 resident species (about one-third of Hispaniola’s low-elevation resident land bird species), of which 5 are endemic to Hispaniola. Two of these endemic species, the Palmchat (Dulus dominicus) and the Hispaniolan Woodpecker (Melanerpes striatus), were the pre- dominant species present. Seventy-six percent of species at this site showed an association with trees. The royal palm occurred mainly in wooded riparian corridors, but showed little ability to colonize pastures, suggesting possible declines in future overall tree density at this site. Ensuring adequate tree recruitment is crucial to maintaining biodiversity in agricultural and grazing zones. -
Dry Forest Trees of Madagascar
The Red List of Dry Forest Trees of Madagascar Emily Beech, Malin Rivers, Sylvie Andriambololonera, Faranirina Lantoarisoa, Helene Ralimanana, Solofo Rakotoarisoa, Aro Vonjy Ramarosandratana, Megan Barstow, Katharine Davies, Ryan Hills, Kate Marfleet & Vololoniaina Jeannoda Published by Botanic Gardens Conservation International Descanso House, 199 Kew Road, Richmond, Surrey, TW9 3BW, UK. © 2020 Botanic Gardens Conservation International ISBN-10: 978-1-905164-75-2 ISBN-13: 978-1-905164-75-2 Reproduction of any part of the publication for educational, conservation and other non-profit purposes is authorized without prior permission from the copyright holder, provided that the source is fully acknowledged. Reproduction for resale or other commercial purposes is prohibited without prior written permission from the copyright holder. Recommended citation: Beech, E., Rivers, M., Andriambololonera, S., Lantoarisoa, F., Ralimanana, H., Rakotoarisoa, S., Ramarosandratana, A.V., Barstow, M., Davies, K., Hills, BOTANIC GARDENS CONSERVATION INTERNATIONAL (BGCI) R., Marfleet, K. and Jeannoda, V. (2020). Red List of is the world’s largest plant conservation network, comprising more than Dry Forest Trees of Madagascar. BGCI. Richmond, UK. 500 botanic gardens in over 100 countries, and provides the secretariat to AUTHORS the IUCN/SSC Global Tree Specialist Group. BGCI was established in 1987 Sylvie Andriambololonera and and is a registered charity with offices in the UK, US, China and Kenya. Faranirina Lantoarisoa: Missouri Botanical Garden Madagascar Program Helene Ralimanana and Solofo Rakotoarisoa: Kew Madagascar Conservation Centre Aro Vonjy Ramarosandratana: University of Antananarivo (Plant Biology and Ecology Department) THE IUCN/SSC GLOBAL TREE SPECIALIST GROUP (GTSG) forms part of the Species Survival Commission’s network of over 7,000 Emily Beech, Megan Barstow, Katharine Davies, Ryan Hills, Kate Marfleet and Malin Rivers: BGCI volunteers working to stop the loss of plants, animals and their habitats. -
Plant Anatomy Lab 13 – Seeds and Fruits
Plant Anatomy Lab 13 – Seeds and Fruits In this (final) lab, you will be observing the structure of seeds of gymnosperms and angiosperms and the fruits of angiosperms. Much of the work will be done with a dissecting microscope, but a few prepared slides will also be used. A set of photocopied images from the plant anatomy atlas will be available as a handout. You can use the handout to help you identify the various structures we will be looking at in seeds and fruits. Also, a fruit key is available as a separate handout. Remember that we will be considering only a small fraction of the structural diversity present among seeds of gymnosperms and the seeds and fruits of angiosperms. Seeds Gymnosperms Obtain a prepared slide of an immature pine ovule and of a mature pine ovule. You will be able to tell them apart from the following observations. • Looking at the immature ovule, you will see a megagametophyte with one or more archegonia at the end near the micropyle. The egg inside may or may not have been fertilized. • Also find the nucellus and integument tissues. Next look at a slide of a mature ovule. Instead of the megagametophyte, you will find a developing embryo. As part of this embryo, find the • cotyledons, • the radicle (embryonic root), and the • shoot apical meristem. Depending on its age, you may also notice procambial strands running between the embryonic root and the shoot apex. Points to consider: We might say that gymnosperms and angiosperms have seeds but only angiosperms have fruits - Why is that? Why don’t we consider the seed cone of a pine tree a fruit? Angiosperms Dicot Obtain a bean pod. -
Karyomorphology of Caesalpinia Species (Caesalpinioideae: Fabaceae) from Caatinga and Mata Atlantica Biomes of Brazil
Journal of Plant Studies; Vol. 1, No. 2; 2012 ISSN 1927-0461 E-ISSN 1927-047X Published by Canadian Center of Science and Education Karyomorphology of Caesalpinia Species (Caesalpinioideae: Fabaceae) from Caatinga and Mata Atlantica Biomes of Brazil Polliana Silva Rodrigues1, Margarete Magalhães Souza2 & Ronan Xavier Corrêa2 1 Programa de Pós-Graduação em Genética e Biologia Molecular, Universidade Estadual de Santa Cruz, Brazil 2 Departamento de Ciências Biológicas, Universidade Estadual de Santa Cruz, Brazil Correspondence: Ronan Xavier Corrêa, Genética e Biologia Molecular, Universidade Estadual de Santa Cruz, Brazil. Tel: 55-733-680-5183. E-mail: [email protected] Received: November 29, 2011 Accepted: December 12, 2011 Online Published: August 10, 2012 doi:10.5539/jps.v1n2p82 URL: http://dx.doi.org/10.5539/jps.v1n2p82 This research was supported by Conselho Nacional de Desenvolvimento Científico (CNPq) (grants numbers CNPq 620147/2004-0 and 473393/2007-7). P.S.R. was awarded MSc. Fellowships from Fundação de Amparo à Pesquisa no Estado da Bahia (FAPESB) and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Abstract Out of 140 Caesalpinia s.l. species, only 20 species have the chromosome numbers presently known, and nine species have the karyomorphological studies available. We determine the karyotype and the chromosome morphometry in five Caesalpinia s.l. spp., and we describe the heterochromatin pattern in four of them. The diploid chromosome number of 24 was reported for the first time in Caesalpinia calycina, Caesalpinia microphylla and Caesalpinia pluviosa var. peltophoroides, and confirmed in Caesalpinia ferrea var. leiostachya and Caesalpinia pulcherrima. Different karyotype formulae were obtained for each of these five species. -
ABSTRACTS 117 Systematics Section, BSA / ASPT / IOPB
Systematics Section, BSA / ASPT / IOPB 466 HARDY, CHRISTOPHER R.1,2*, JERROLD I DAVIS1, breeding system. This effectively reproductively isolates the species. ROBERT B. FADEN3, AND DENNIS W. STEVENSON1,2 Previous studies have provided extensive genetic, phylogenetic and 1Bailey Hortorium, Cornell University, Ithaca, NY 14853; 2New York natural selection data which allow for a rare opportunity to now Botanical Garden, Bronx, NY 10458; 3Dept. of Botany, National study and interpret ontogenetic changes as sources of evolutionary Museum of Natural History, Smithsonian Institution, Washington, novelties in floral form. Three populations of M. cardinalis and four DC 20560 populations of M. lewisii (representing both described races) were studied from initiation of floral apex to anthesis using SEM and light Phylogenetics of Cochliostema, Geogenanthus, and microscopy. Allometric analyses were conducted on data derived an undescribed genus (Commelinaceae) using from floral organs. Sympatric populations of the species from morphology and DNA sequence data from 26S, 5S- Yosemite National Park were compared. Calyces of M. lewisii initi- NTS, rbcL, and trnL-F loci ate later than those of M. cardinalis relative to the inner whorls, and sepals are taller and more acute. Relative times of initiation of phylogenetic study was conducted on a group of three small petals, sepals and pistil are similar in both species. Petal shapes dif- genera of neotropical Commelinaceae that exhibit a variety fer between species throughout development. Corolla aperture of unusual floral morphologies and habits. Morphological A shape becomes dorso-ventrally narrow during development of M. characters and DNA sequence data from plastid (rbcL, trnL-F) and lewisii, and laterally narrow in M. -
Red Palm Mite)
Crop Protection Compendium Datasheet report for Raoiella indica (red palm mite) Top of page Pictures Picture Title Caption Copyright Adult The red palm mite (Raoiella indica), an invasive species in the Caribbean, may threaten USDA- mite several important palms found in the southern USA. (Original magnified approx. 300x.) ARS Photo by Eric Erbe; Digital colourization by Chris Pooley. Colony Colony of red palm mites (Raoiella indica) on coconut leaflet, from India. Bryony of Taylor mites Colony Close-up of a colony of red palm mites (Raoiella indica) on coconut leaflet, from India. Bryony of Taylor mites Top of page Identity Preferred Scientific Name Raoiella indica Hirst (1924) Preferred Common Name red palm mite International Common Names English: coconut red mite; frond crimson mite; leaflet false spider mite; red date palm mite; scarlet mite EPPO code RAOIIN (Raoiella indica) Top of page Taxonomic Tree Domain: Eukaryota Kingdom: Metazoa Phylum: Arthropoda Subphylum: Chelicerata Class: Arachnida Subclass: Acari Superorder: Acariformes Suborder: Prostigmata Family: Tenuipalpidae Genus: Raoiella Species: Raoiella indica / Top of page Notes on Taxonomy and Nomenclature R. indica was first described in the district of Coimbatore (India) by Hirst in 1924 on coconut leaflets [Cocos nucifera]. A comprehensive taxonomic review of the genus and species was carried out by Mesa et al. (2009), which lists all suspected junior synonyms of R. indica, including Raoiella camur (Chaudhri and Akbar), Raoiella empedos (Chaudhri and Akbar), Raoiella obelias (Hasan and Akbar), Raoiella pandanae (Mohanasundaram), Raoiella phoenica (Meyer) and Raoiella rahii (Akbar and Chaudhri). The review also highlighted synonymy with Rarosiella cocosae found on coconut in the Philippines.