Vol58n2p77-85
Total Page:16
File Type:pdf, Size:1020Kb

Load more
Recommended publications
-
Approved Plant List 10/04/12
FLORIDA The best time to plant a tree is 20 years ago, the second best time to plant a tree is today. City of Sunrise Approved Plant List 10/04/12 Appendix A 10/4/12 APPROVED PLANT LIST FOR SINGLE FAMILY HOMES SG xx Slow Growing “xx” = minimum height in Small Mature tree height of less than 20 feet at time of planting feet OH Trees adjacent to overhead power lines Medium Mature tree height of between 21 – 40 feet U Trees within Utility Easements Large Mature tree height greater than 41 N Not acceptable for use as a replacement feet * Native Florida Species Varies Mature tree height depends on variety Mature size information based on Betrock’s Florida Landscape Plants Published 2001 GROUP “A” TREES Common Name Botanical Name Uses Mature Tree Size Avocado Persea Americana L Bahama Strongbark Bourreria orata * U, SG 6 S Bald Cypress Taxodium distichum * L Black Olive Shady Bucida buceras ‘Shady Lady’ L Lady Black Olive Bucida buceras L Brazil Beautyleaf Calophyllum brasiliense L Blolly Guapira discolor* M Bridalveil Tree Caesalpinia granadillo M Bulnesia Bulnesia arboria M Cinnecord Acacia choriophylla * U, SG 6 S Group ‘A’ Plant List for Single Family Homes Common Name Botanical Name Uses Mature Tree Size Citrus: Lemon, Citrus spp. OH S (except orange, Lime ect. Grapefruit) Citrus: Grapefruit Citrus paradisi M Trees Copperpod Peltophorum pterocarpum L Fiddlewood Citharexylum fruticosum * U, SG 8 S Floss Silk Tree Chorisia speciosa L Golden – Shower Cassia fistula L Green Buttonwood Conocarpus erectus * L Gumbo Limbo Bursera simaruba * L -
A Conservation Framework for the Critically Endangered Endemic Species of the Caribbean Palm Coccothrinax
A conservation framework for the Critically Endangered endemic species of the Caribbean palm Coccothrinax B RETT J ESTROW,BRÍGIDO P EGUERO,FRANCISCO J IMÉNEZ,RAÚL V ERDECIA L ISBET G ONZÁLEZ-OLIVA,CELIO E. MOYA,WILLIAM C INEA,M.PATRICK G RIFFITH A LAN W. MEEROW,MIKE M AUNDER and J AVIER F RANCISCO-ORTEGA Abstract With threatened species ( categorized as plant exploration initiatives, taxonomic revisions, outreach, Critically Endangered and as Endangered, sensu IUCN), and fundraising. The ultimate aim of this review is to provide Coccothrinax (c. species) is the flagship palm genus for baseline information that will develop conservation synergy conservation in the Caribbean Island Biodiversity Hotspot. among relevant parties working on Coccothrinax conserva- Coccothrinax has its centre of taxonomic diversity in these tion in Cuba, Haiti and the Dominican Republic. Such colla- islands, with c. endemic species. We present a conservation borations could also benefit through partnerships with framework for the Critically Endangered species, found botanists working in other countries. in Cuba, Haiti or the Dominican Republic. Only two species Keywords Antilles, Arecaceae, IUCN, plant biodiversity, (C. jimenezii, C. montana) occur in more than one country red lists, taxonomy, tropical islands (Haiti and the Dominican Republic). Immediate threats include oil drilling and nickel mining, intrusion of saline water into soil, urban and agricultural development, low population recruitment, uncontrolled fires, interspecific hy- Introduction bridization, and unsustainable ethnobotanical practices. Coccothrinax bermudezii, C. borhidiana, C. crinita ssp. crini- alms are an iconic feature of the Caribbean landscape ta, C. leonis and C. spissa are not conserved in protected areas. Pand are associated with strong folk and ethnobotani- Coccothrinax bermudezii, C. -
Belize), and Distribution in Yucatan
University of Neuchâtel, Switzerland Institut of Zoology Ecology of the Black Catbird, Melanoptila glabrirostris, at Shipstern Nature Reserve (Belize), and distribution in Yucatan. J.Laesser Annick Morgenthaler May 2003 Master thesis supervised by Prof. Claude Mermod and Dr. Louis-Félix Bersier CONTENTS INTRODUCTION 1. Aim and description of the study 2. Geographic setting 2.1. Yucatan peninsula 2.2. Belize 2.3. Shipstern Nature Reserve 2.3.1. History and previous studies 2.3.2. Climate 2.3.3. Geology and soils 2.3.4. Vegetation 2.3.5. Fauna 3. The Black Catbird 3.1. Taxonomy 3.2. Description 3.3. Breeding 3.4. Ecology and biology 3.5. Distribution and threats 3.6. Current protection measures FIRST PART: BIOLOGY, HABITAT AND DENSITY AT SHIPSTERN 4. Materials and methods 4.1. Census 4.1.1. Territory mapping 4.1.2. Transect point-count 4.2. Sizing and ringing 4.3. Nest survey (from hide) 5. Results 5.1. Biology 5.1.1. Morphometry 5.1.2. Nesting 5.1.3. Diet 5.1.4. Competition and predation 5.2. Habitat use and population density 5.2.1. Population density 5.2.2. Habitat use 5.2.3. Banded individuals monitoring 5.2.4. Distribution through the Reserve 6. Discussion 6.1. Biology 6.2. Habitat use and population density SECOND PART: DISTRIBUTION AND HABITATS THROUGHOUT THE RANGE 7. Materials and methods 7.1. Data collection 7.2. Visit to others sites 8. Results 8.1. Data compilation 8.2. Visited places 8.2.1. Corozalito (south of Shipstern lagoon) 8.2.2. -
Journal of the International Palm Society Vol. 58(4) Dec. 2014 the INTERNATIONAL PALM SOCIETY, INC
Palms Journal of the International Palm Society Vol. 58(4) Dec. 2014 THE INTERNATIONAL PALM SOCIETY, INC. The International Palm Society Palms (formerly PRINCIPES) Journal of The International Palm Society Founder: Dent Smith The International Palm Society is a nonprofit corporation An illustrated, peer-reviewed quarterly devoted to engaged in the study of palms. The society is inter- information about palms and published in March, national in scope with worldwide membership, and the June, September and December by The International formation of regional or local chapters affiliated with the Palm Society Inc., 9300 Sandstone St., Austin, TX international society is encouraged. Please address all 78737-1135 USA. inquiries regarding membership or information about Editors: John Dransfield, Herbarium, Royal Botanic the society to The International Palm Society Inc., 9300 Gardens, Kew, Richmond, Surrey, TW9 3AE, United Sandstone St., Austin, TX 78737-1135 USA, or by e-mail Kingdom, e-mail [email protected], tel. 44-20- to [email protected], fax 512-607-6468. 8332-5225, Fax 44-20-8332-5278. OFFICERS: Scott Zona, Dept. of Biological Sciences (OE 167), Florida International University, 11200 SW 8 Street, President: Leland Lai, 21480 Colina Drive, Topanga, Miami, Florida 33199 USA, e-mail [email protected], tel. California 90290 USA, e-mail [email protected], 1-305-348-1247, Fax 1-305-348-1986. tel. 1-310-383-2607. Associate Editor: Natalie Uhl, 228 Plant Science, Vice-Presidents: Jeff Brusseau, 1030 Heather Drive, Cornell University, Ithaca, New York 14853 USA, e- Vista, California 92084 USA, e-mail mail [email protected], tel. 1-607-257-0885. -
Thrinax Radiata Family: Arecaceae Florida Thatch Palm, Jamaican Thatch, Thatch Palm, Chit
Stephen H. Brown, Horticulture Agent Donna Cressman, Master Gardener Lee County Extension, Fort Myers, Florida (239) 533-7513 [email protected] http://lee.ifas.ufl.edu/hort/GardenHome.shtml Thrinax radiata Family: Arecaceae Florida thatch palm, Jamaican thatch, thatch palm, chit Florida Thatch Palm Synonyms (Discarded names): Cocothrinax martii, C. radiate, Thrinax floridana, T. martii, T. multiflora; T. wendlandiana Origin: Extreme southern mainland coast of Florida, Florida Keys, Bahamas, western Cuba, Cayman Islands, Jamaica, Hispaniola, Puerto Rico, Yucatan Peninsula, Honduras, Nicaragua U.S.D.A. Zone: 10A-12B (28°F leaf damage) Growth Rate: Slow Typical Height: 20’ Habit: Solitary; canopy of 12-20 leaves Crownshaft: None Leaf: Palmate, induplicate, circular, slightly folded; divided about halfway into segments that are split at the tips; pointed hastula Leaf Size: 4-5’ wide; segments 2.5’ long, 2” wide Salt Tolerance: High Drought Tolerance: High Wind Tolerance: High Light Requirements: Moderate, high Soil: Widely adaptable Nutritional Requirements: Low Potential Insect Pests: Aphids; scales Propagation: Seeds Human hazards: None Uses: Small gardens; containers; outdoors patios; roadways; parking lots; seasides; specimen Left: The infructescence (fruited stems) hang in a circle around the trunk, sometimes extending beyond the leaf. Natural Geographic Distribution The Florida Thatch Palm, Thrinax radiata, is indigenous to the extreme southern mainland coast of Florida, the Florida Keys, Bahamas, western Cuba, The Cayman Islands, Jamaica, Hispaniola, Puerto Rico, Honduras, Nicaragua, and the eastern coast of the Yucatan Peninsula in Mexico and Belize. In na- ture, this palm almost always grows within the range of salt-laden winds near coastal areas. It grows naturally in sandy or calcareous soils. -
Tropical Plant-Animal Interactions: Linking Defaunation with Seed Predation, and Resource- Dependent Co-Occurrence
University of Montana ScholarWorks at University of Montana Graduate Student Theses, Dissertations, & Professional Papers Graduate School 2021 TROPICAL PLANT-ANIMAL INTERACTIONS: LINKING DEFAUNATION WITH SEED PREDATION, AND RESOURCE- DEPENDENT CO-OCCURRENCE Peter Jeffrey Williams Follow this and additional works at: https://scholarworks.umt.edu/etd Let us know how access to this document benefits ou.y Recommended Citation Williams, Peter Jeffrey, "TROPICAL PLANT-ANIMAL INTERACTIONS: LINKING DEFAUNATION WITH SEED PREDATION, AND RESOURCE-DEPENDENT CO-OCCURRENCE" (2021). Graduate Student Theses, Dissertations, & Professional Papers. 11777. https://scholarworks.umt.edu/etd/11777 This Dissertation is brought to you for free and open access by the Graduate School at ScholarWorks at University of Montana. It has been accepted for inclusion in Graduate Student Theses, Dissertations, & Professional Papers by an authorized administrator of ScholarWorks at University of Montana. For more information, please contact [email protected]. TROPICAL PLANT-ANIMAL INTERACTIONS: LINKING DEFAUNATION WITH SEED PREDATION, AND RESOURCE-DEPENDENT CO-OCCURRENCE By PETER JEFFREY WILLIAMS B.S., University of Minnesota, Minneapolis, MN, 2014 Dissertation presented in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Biology – Ecology and Evolution The University of Montana Missoula, MT May 2021 Approved by: Scott Whittenburg, Graduate School Dean Jedediah F. Brodie, Chair Division of Biological Sciences Wildlife Biology Program John L. Maron Division of Biological Sciences Joshua J. Millspaugh Wildlife Biology Program Kim R. McConkey School of Environmental and Geographical Sciences University of Nottingham Malaysia Williams, Peter, Ph.D., Spring 2021 Biology Tropical plant-animal interactions: linking defaunation with seed predation, and resource- dependent co-occurrence Chairperson: Jedediah F. -
Tourism and Forest Livelihoods: Linking Architecture with Tropical Forest Management
TOURISM AND FOREST LIVELIHOODS: LINKING ARCHITECTURE WITH TROPICAL FOREST MANAGEMENT By JOSÉ ANTONIO SIERRA HUELSZ A DISSERTATION PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY UNIVERSITY OF FLORIDA 2016 © 2016 José Antonio Sierra Huelsz To Mane and Mateo, my sources of inspiration and love To my parents for their ever loving support ACKNOWLEDGMENTS I am deeply grateful to my exceptional advisor Dr. Karen A. Kainer for her generous mentoring, for being a great teacher, colleague and friend. My committee contributed substantially to the conception of this dissertation, pushing me to think in new directions. I am very thankful to Erick Keys, Francis “Jack” Putz, Patricia Negreros- Castillo and Salvador Gezan for their stimulating perspectives and feedback. In particular, I am in debt with Dr. Negreros-Castillo for inspiring me to work in Quintana Roo and facilitating my landing in the Zona Maya. I would like to thank Wendell P. Cropper for his kind support at the early stages of this journey. This dissertation was enriched by the time, knowledge, and creativity of Sebastián Palmas Pérez, Angélica Navarro Martinez, Pedro Antonio Macario Mendoza, and Mirna Valdez Hernández - all who kindly collaborated in this process. Santos Colli Balam has been an irreplaceable friend, bush colleague, and cultural ambassador. Without Angel David Cab Argüelles, Edgar Can Balam, and the ever supportive X-Pichil crew, my fieldwork plans would be just an unrealized dream. Tarín Toledo Aceves, Eddie A. Ellis and Horacio Paz Hernández kindly provided essential support for accessing funds that helped make this project possible; many thanks to you all. -
Native Trees of Mexico: Diversity, Distribution, Uses and Conservation
Native trees of Mexico: diversity, distribution, uses and conservation Oswaldo Tellez1,*, Efisio Mattana2,*, Mauricio Diazgranados2, Nicola Kühn2, Elena Castillo-Lorenzo2, Rafael Lira1, Leobardo Montes-Leyva1, Isela Rodriguez1, Cesar Mateo Flores Ortiz1, Michael Way2, Patricia Dávila1 and Tiziana Ulian2 1 Facultad de Estudios Superiores Iztacala, Av. De los Barrios 1, Los Reyes Iztacala Tlalnepantla, Universidad Nacional Autónoma de México, Estado de México, Mexico 2 Wellcome Trust Millennium Building, RH17 6TN, Royal Botanic Gardens, Kew, Ardingly, West Sussex, United Kingdom * These authors contributed equally to this work. ABSTRACT Background. Mexico is one of the most floristically rich countries in the world. Despite significant contributions made on the understanding of its unique flora, the knowledge on its diversity, geographic distribution and human uses, is still largely fragmented. Unfortunately, deforestation is heavily impacting this country and native tree species are under threat. The loss of trees has a direct impact on vital ecosystem services, affecting the natural capital of Mexico and people's livelihoods. Given the importance of trees in Mexico for many aspects of human well-being, it is critical to have a more complete understanding of their diversity, distribution, traditional uses and conservation status. We aimed to produce the most comprehensive database and catalogue on native trees of Mexico by filling those gaps, to support their in situ and ex situ conservation, promote their sustainable use, and inform reforestation and livelihoods programmes. Methods. A database with all the tree species reported for Mexico was prepared by compiling information from herbaria and reviewing the available floras. Species names were reconciled and various specialised sources were used to extract additional species information, i.e. -
Floral Anatomy of Chelyocarpus, Cryosophila, and Ltaya (Palmae)
19721 UHL: FLORAL ANATON,IY B9 Floral Anatomy of Chelyocarpus, Cryosophila, and ltaya (Palmae) Nlrar,rs W. Unr-* L. H. Bailey Hortorium, Cornell Uniuersity, Ithaca, New York 14850 This paper presentsthe floral anatomy Descripfions ol the Chelyocctrpus alliance to accom- CuBlvoc.q.npus(Fig. 1-7) . pany a current assessmentof the group including the descriptionof a new genus Chelyocarpwsulei is described from t'Moore, L972). Although reports of Moore anil Salazar 9494. Flowers, each floral anatomy in palms are few, those 4-5 mm. long and 2 by 4 mm. wide, completed have been valuable in deter- have two broadly ovate sepals, 2 rrrm' mining functions of floral organs and long by 2 mm. wide, which are distinct relationships among genera, and have or slightly joined at the base forming a provided new information on floral shallow cup around two distinct ovate structure in angiosperms (Uhl and petalsof aboutthe samesize. The androe- Moore, 1971). As the accompanying cium consists of seven (five-eight) paper (Moore, 1972) explains, the stamens in a distinctive arrangement. genera considered here are of special One stamen is opposite and sheathedby interest becausethey may form a primi- each sepal and the others form two rows tive alliance within the palms, and of two to three stamenseach, one row becausetwo species,ClrcIyocarpus dia- opposite each petal (Fig. 6). The nuerus and C. zrlel possessflor,al plans flower is thus wider along the axis of that are unique in rthefamily. petal insertion. Filaments of the stamens (Fig. 3a, b) are 2.5 mm.long, ventrally Mqteriqls qnd Methods expanded, and tightly encase the lower two-thirds of two (three, four) carpels. -
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. -
Anatomía Y Usos De Las Hojas Maduras De Tres Especies De Sabal (Arecaceae) De La Península De Yucatán, México
Rev. Biol. Trop. 51(2): 333-344, 2003 www.ucr.ac.cr www.ots.ac.cr www.ots.duke.edu Anatomía y usos de las hojas maduras de tres especies de Sabal (Arecaceae) de la Península de Yucatán, México Martha Pérez & Silvia Rebollar Departamento de Biología, Universidad Autónoma Metropolitana-Iztapalapa. A. P. 55-535. 09340, México, D. F. Fax: 58- 04-46-88; [email protected]; [email protected] Recibido 12-VI-2001. Corregido 06-III-2002. Aceptado 13-VI-2002. Abstract: This paper describes the leaf anatomy of Sabal mauritiiformis (Karst.) Griseb. & H. Wendl., Sabal mexicana Mart. and Sabal yapa Wright ex Becc., three of the four most representative species of the Yucatán Península, in Mexico. These species are locally used: in the roofing of traditional homes, as food (fruits and api- cal buds), and in the production of hats, brooms and handicrafts. Leaf samples were collected in secondary growth of lower montane rainforest in the state of Quintana Roo and in two home gardens in the state of Yuca- tán. Herbarium samples were obtained, and samples of blade and petiole were fixed in formaline-acetic acid-al- cohol. Cross incisions were made on the blade and petiole, and were dyed with safranin and toluidine blue O. The results show that S. mauritiiformis and S. yapa are morphologically alike: both are tall, slim palm trees; the leaf in S. mauritiiformis is a shorter palm-like structure compared with the other two species. The shape of the main nerve, as seen in cross section, is rectangular in the three species. -
Lista De Palmas Cubanas I- Hemithrinax
ISSN 2519-7754 RNPS 2402 www.revistas.geotech.cu/index.php/abc ║LISTA DE ESPECIES║ Vol. 218, No.1 (enero-abril 2019): 1-10 Lista de Palmas Cubanas. I. Hemithrinax, Leucothrinax y Thrinax Cuban Palms Checklist. I. Hemithrinax, Leucothrinax and Thrinax Celio E. Moya López R SU N Autor para correspondencia: [email protected] Se actualiza la lista de táxones y de sinónimos nomenclaturales de los géneros Hemithrinax, Leucothrinax y Thrinax. Se designaron los lectotipos de Hemithrinax compacta y Leucothrinax morrisii, y se precisaron los lectotipos de otros nueve nombres. Sociedad Cubana de Botánica Calle Cuba 406 e/ Amargura y Brasil, Palabras clave: Arecaceae, Hemithrinax, Leucothrinax, Thrinax La Habana Vieja, La Habana, Cuba A S RAC Recibido: 01/06/2018 Aceptado: 21/01/2019 The list of taxa and nomenclatural synonyms of the genera Hemithrinax, Leucothrinax and Thrinax is updated. The lectotype of Hemithrinax compacta were designated and lectotypes of other ten names were specified. Key words: Arecaceae, Hemithrinax, Leucothrinax, Thrinax INTRODUCCIÓN Hemithrinax es un género endémico cubano, representa- do por tres especies y una variedad reconocida. Sus La familia Arecaceae Schultz Sch. (nom. cons.) está táxones se diferencian fácilmente de los de Thrinax o representada en Cuba por 15 géneros con 80 especies, Leucothrinax por presentar las venas transversales poco ocho híbridos y nueve táxones infraespecíficos (Moya y visibles, mientras que en éstos las venas transversales Leiva, 2000). De ellos, tres constituyen nuevos registros o son conspicuas (Lewis y Zona, 2008). cambios de estatus posteriores (Suárez, 2015; Verdecia, 2016; Moya et al., 2017; Moya y Méndez, 2018), lo cual Leucothrinax es un género monotípico, de distribución sugiere que la riqueza taxonómica de la familia en Cuba caribeña, representado por Leucothrinax morrisii aún no es totalmente conocida.