Trinidad and Tobago to the CBD Acknowledgements
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Lepidoptera: Papilionoidea) Q ⇑ Marianne Espeland A,B, , Jason P.W
Molecular Phylogenetics and Evolution 93 (2015) 296–306 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Ancient Neotropical origin and recent recolonisation: Phylogeny, biogeography and diversification of the Riodinidae (Lepidoptera: Papilionoidea) q ⇑ Marianne Espeland a,b, , Jason P.W. Hall c, Philip J. DeVries d, David C. Lees e, Mark Cornwall a, Yu-Feng Hsu f, Li-Wei Wu g, Dana L. Campbell a,h, Gerard Talavera a,i,j, Roger Vila i, Shayla Salzman a, Sophie Ruehr k, David J. Lohman l, Naomi E. Pierce a a Museum of Comparative Zoology and Department of Organismic and Evolutionary Biology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA b McGuire Center for Lepidoptera and Biodiversity, Florida Museum of Natural History, University of Florida, Powell Hall, 2315 Hull Road, Gainesville, FL 32611, USA c Department of Systematic Biology-Entomology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20560-127, USA d Department of Biological Sciences, University of New Orleans, 2000 Lake Shore Drive, New Orleans, LA 70148, USA e Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, UK f Department of Life Science, National Taiwan Normal University, Taipei, Taiwan g The Experimental Forest, College of Bio-Resources and Agriculture, National Taiwan University, Nantou, Taiwan h Division of Biological Sciences, School of Science, Technology, Engineering & Mathematics, University of Washington Bothell, Box 358500, 18115 Campus Way NE, Bothell, WA 98011-8246, USA i Institut de Biologia Evolutiva (CSIC-UPF), Pg. Marítim de la Barceloneta 37, 08003 Barcelona, Spain j Faculty of Biology & Soil Science, St. -
The Lesser Antilles Incuding Trinidad
The brilliant Lesser Antillean Barn Owl again showed superbly. One of several potential splits not yet recognized by the IOC (Pete Morris) THE LESSER ANTILLES INCUDING TRINIDAD 5 – 20/25 JUNE 2015 LEADERS: PETE MORRIS After our successful tour around the Caribbean in 2013, it was great to get back again this year. It all seemed pretty straightforward this time around, and once again we cleaned up on all of the available endemics, po- 1 BirdQuest Tour Report:The Lesser Antilles www.birdquest-tours.com The fabulous White-breasted Thrasher from Martinique (Pete Morris) tential splits and other goodies. For sure, this was no ordinary Caribbean holiday! During the first couple of weeks we visited no fewer than ten islands (Antigua, Barbuda, Montserrat, Dominica, Guadeloupe, Martinique, St Lucia, St Vincent, Barbados and Grenada), a logistical feat of some magnitude. With plenty of LIAT flights (the islanders refer to LIAT as ‘Leave Island any Time’ and ‘Luggage in Another Terminal’ to name but two of the many funny phrases coined from LIAT) and unreliable AVIS car hire reservations, we had our work cut out, but in the end, all worked out! It’s always strange birding on islands with so few targets, but with so many islands to pack-in, we were never really short of things to do. All of the endemics showed well and there were some cracking highlights, including the four smart endemic amazons, the rare Grenada Dove, the superb Lesser Antillean Barn Owl, the unique tremblers and White-breasted Thrashers, and a series of colourful endemic orioles to name just a few! At the end of the Lesser Antilles adventure we enjoyed a few days on Trinidad. -
Bioone? RESEARCH
RESEARCH BioOne? EVOLVED Proximate Nutrient Analyses of Four Species of Submerged Aquatic Vegetation Consumed by Florida Manatee (Trichechus manatus latirostris) Compared to Romaine Lettuce (Lactuca sativa var. longifolia) Author(s): Jessica L. Siegal-Willott, D.V.M., Dipl. A.C.Z.M., Kendal Harr, D.V.M., M.S., Dipl. A.C.V.P., Lee-Ann C. Hayek, Ph.D., Karen C. Scott, Ph.D., Trevor Gerlach, B.S., Paul Sirois, M.S., Mike Renter, B.S., David W. Crewz, M.S., and Richard C. Hill, M.A., Vet.M.B., Ph.D., M.R.C.V.S. Source: Journal of Zoo and Wildlife Medicine, 41(4):594-602. 2010. Published By: American Association of Zoo Veterinarians DOI: 10.1638/2009-0118.1 URL: http://www.bioone.org/doi/full/10.1638/2009-0118.1 BioOne (www.bioone.org) is an electronic aggregator of bioscience research content, and the online home to over 160 journals and books published by not-for-profit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne's Terms of Use, available at www.bioone.org/page/terms of use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. -
Buccoo Reef/ Bon Accord Lagoon Complex
BUCCOO REEF/ BON ACCORD LAGOON COMPLEX Geographical Location: Tobago Name of the Ramsar site: Buccoo Reef/Bon Accord Lagoon Complex Ramsar Site No.: 1496 Geographical coordinates (latitude/longitude): 11° 10′ N, 60° 57′ W, Total site area: 1287 hectares 2 Area: 12.87 km (1287 ha). Mean sea level to 30 m below sea level Mangroves 2 2 2 account for 1.3 km (130 ha) of which 0.1 km (10 ha) are ponds and 0.5 km (50 ha) are seagrass beds General location: The wetland is located on the leeward coast of south-western Tobago and approximately 6 miles (in a straight line) from the administrative town of Scarborough, which is in the parish of St. Andrew. Adjacent to the wetland are the villages of Buccoo and Canaan/Bon Accord which are considered population growth poles in Tobago (IMA, 1996). Summary description: Buccoo Reef / Bon Accord Lagoon Complex. 1,287 ha; 11°10'N 060°57'W. Restricted Area (in the process of being designated as Environmentally Sensitive Area). Located on the south-western coast of Tobago near Scarborough, this site contains several under-represented wetland types such as coral reefs, seagrass beds and mangrove forests. Endangered and vulnerable species in the area include various types of coral (Acropora palmata, Diploria labyrinthiformis, D. strigosa and Siderastrea siderea) as well as the critically endangered Hawksbill turtle (Eretmochelys imbricata) and at least 119 fish species. As the major tourist attraction in Tobago, the reef continues to be adversely affected by intense tourist activity and pollutant discharges. So far the restricted area status and existing management plan have been unable to prevent these impacts. -
National Biodiversity Strategy and Action Plan for Trinidad and Tobago, 2017-2022
National Biodiversity Strategy and Action Plan for Trinidad and Tobago, 2017-2022 1 National Biodiversity Strategy and Action Plan for Trinidad and Tobago, 2017-2022 Table of Contents Table of Contents ..................................................................................................................................... 2 ACRONYMS ................................................................................................................................................. 4 1. EXECUTIVE SUMMARY ................................................................................................................. 5 List of Tables ............................................................................................................................................ 11 List of Figures .......................................................................................................................................... 12 2. INTRODUCTION ............................................................................................................................ 15 2.2 Value of biodiversity to T&T ............................................................................................ 15 2.2.1 Ecosystem Services ..................................................................................................... 16 Terrestrial ............................................................................................................................................ 16 2.2.2 Tourism .......................................................................................................................... -
Willmott, K. R., and J. P. W. Hall. 1994. Four New Species of Riodinids
Vol. 5 No. 2 1994 WILLMOTT and HALL: New Ecuadorian Riodinidae 87 TROPICAL LEPIDOPTERA, 5(2): 87-91 FOUR NEW SPECIES OF RIODINIDS FROM WESTERN ECUADOR (LEPIDOPTERA: RIODINIDAE) KEITH R. WILLMOTT and JASON P. W. HALL Dept. of Entomology and Nematology, University of Florida, Gainseville, Florida 32611, USA ABSTRACT.- Four new species of Riodinidae in the genera Theope Doubleday, 1847, Mesosemia Hilbner, [1819], and Symmachia Htibner, [1819], are named and described from western Ecuador, with additional observations on behavior. KEY WORDS: behavior, Calospila, Central America, Colombia, Mesoamerica, Mesosemia hazelae n. sp., Neotropical, Panama, perching behavior, Symmachia wiltoni n. sp., Symmachiini, taxonomy, Theope iani n. sp., Theope pepo n. sp. Fig. 1-2. La Punta, W. Ecuador: 1. View out over the canopy from the ridgetop site; 2. Symmachia wiltoni Willmott & Hall: male perching under a leaf. The fauna of western Ecuador has clear affinities with southern recently been made in this remarkable family (Salazar, 1993; Central America, but also has a number of endemic species, and Salazar and Constantino, 1993). After consultation of relevant others found only as far north as western Colombia. The first type material and original descriptions, we herein describe four lepidopterists (de Mathan, Haensch, Flemming and Rosenberg) to new species of riodinid from western Ecuador. All these species collect in this area brought numerous new discoveries back to may be easily identified by their distinctive external morphology, Europe around the turn of the century. This still constitutes a but drawings of genitalia are included for the sake of complete- large percent of our knowledge. In more recent times collecting ness. -
Global Seagrass Distribution and Diversity: a Bioregional Model ⁎ F
Journal of Experimental Marine Biology and Ecology 350 (2007) 3–20 www.elsevier.com/locate/jembe Global seagrass distribution and diversity: A bioregional model ⁎ F. Short a, , T. Carruthers b, W. Dennison b, M. Waycott c a Department of Natural Resources, University of New Hampshire, Jackson Estuarine Laboratory, Durham, NH 03824, USA b Integration and Application Network, University of Maryland Center for Environmental Science, Cambridge, MD 21613, USA c School of Marine and Tropical Biology, James Cook University, Townsville, 4811 Queensland, Australia Received 1 February 2007; received in revised form 31 May 2007; accepted 4 June 2007 Abstract Seagrasses, marine flowering plants, are widely distributed along temperate and tropical coastlines of the world. Seagrasses have key ecological roles in coastal ecosystems and can form extensive meadows supporting high biodiversity. The global species diversity of seagrasses is low (b60 species), but species can have ranges that extend for thousands of kilometers of coastline. Seagrass bioregions are defined here, based on species assemblages, species distributional ranges, and tropical and temperate influences. Six global bioregions are presented: four temperate and two tropical. The temperate bioregions include the Temperate North Atlantic, the Temperate North Pacific, the Mediterranean, and the Temperate Southern Oceans. The Temperate North Atlantic has low seagrass diversity, the major species being Zostera marina, typically occurring in estuaries and lagoons. The Temperate North Pacific has high seagrass diversity with Zostera spp. in estuaries and lagoons as well as Phyllospadix spp. in the surf zone. The Mediterranean region has clear water with vast meadows of moderate diversity of both temperate and tropical seagrasses, dominated by deep-growing Posidonia oceanica. -
Bulletin Biological Assessment Boletín RAP Evaluación Biológica
Rapid Assessment Program Programa de Evaluación Rápida Evaluación Biológica Rápida de Chawi Grande, Comunidad Huaylipaya, Zongo, La Paz, Bolivia RAP Bulletin A Rapid Biological Assessment of of Biological Chawi Grande, Comunidad Huaylipaya, Assessment Zongo, La Paz, Bolivia Boletín RAP de Evaluación Editores/Editors Biológica Claudia F. Cortez F., Trond H. Larsen, Eduardo Forno y Juan Carlos Ledezma 70 Conservación Internacional Museo Nacional de Historia Natural Gobierno Autónomo Municipal de La Paz Rapid Assessment Program Programa de Evaluación Rápida Evaluación Biológica Rápida de Chawi Grande, Comunidad Huaylipaya, Zongo, La Paz, Bolivia RAP Bulletin A Rapid Biological Assessment of of Biological Chawi Grande, Comunidad Huaylipaya, Assessment Zongo, La Paz, Bolivia Boletín RAP de Evaluación Editores/Editors Biológica Claudia F. Cortez F., Trond H. Larsen, Eduardo Forno y Juan Carlos Ledezma 70 Conservación Internacional Museo Nacional de Historia Natural Gobierno Autónomo Municipal de La Paz The RAP Bulletin of Biological Assessment is published by: Conservation International 2011 Crystal Drive, Suite 500 Arlington, VA USA 22202 Tel: +1 703-341-2400 www.conservation.org Cover Photos: Trond H. Larsen (Chironius scurrulus). Editors: Claudia F. Cortez F., Trond H. Larsen, Eduardo Forno y Juan Carlos Ledezma Design: Jaime Fernando Mercado Murillo Map: Juan Carlos Ledezma y Veronica Castillo ISBN 978-1-948495-00-4 ©2018 Conservation International All rights reserved. Conservation International is a private, non-proft organization exempt from federal income tax under section 501c(3) of the Internal Revenue Code. The designations of geographical entities in this publication, and the presentation of the material, do not imply the expression of any opinion whatsoever on the part of Conservation International or its supporting organizations concerning the legal status of any country, territory, or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. -
Karyotype Variations in Seagrass (Halodule Wrightii Ascherson¬タヤ
Aquatic Botany 136 (2017) 52–55 Contents lists available at ScienceDirect Aquatic Botany journal homepage: www.elsevier.com/locate/aquabot Short communication Karyotype variations in seagrass (Halodule wrightii Ascherson—Cymodoceaceae) a b,∗ a Silmar Luiz da Silva , Karine Matos Magalhães , Reginaldo de Carvalho a Graduate Program in Botany—PPGB and Cytogenetic Plant Laboratory of the Federal Rural University of Pernambuco, Rua Dom Manoel de Medeiros, s/n, Dois Irmãos, CEP: 52171-900, Recife, Pernambuco, Brazil b Aquatic Ecosystems Laboratory of the Federal Rural University of Pernambuco, Rua Dom Manoel de Medeiros, s/n, Dois Irmãos, CEP: 52171-900, Recife, Pernambuco, Brazil a r t i c l e i n f o a b s t r a c t Article history: Karyotype variations in plants are common, but the results of cytological studies of some seagrasses Received 26 June 2015 remain unclear. The nature of the variation is not clearly understood, and the basic chromosomal num- Received in revised form 5 August 2016 ber has still not been established for the majority of the species. Here, we describe karyotype variations in Accepted 15 September 2016 the seagrass Halodule wrightii, and we suggest potentially causative mechanisms involving cytomixis and Available online 16 September 2016 B chromosomes. We prepared slides using the squashing technique followed by conventional Giemsa and C-banding, and silver nitrate and a CMA/DAPI staining. Based on intraspecific analysis, the diploid chromo- Keywords: some number of H. wrightii exhibited a variation from 2n = 24 to 2n = 39; 2n = 38 was the most frequent. In Cytomixis Seagrass general, we characterized the karyotype as an asymmetrical, semi-reticulated interphase nucleus with a chromosomally uniform condensation pattern. -
INSECTA MUNDIA Journal of World Insect Systematics
INSECTA MUNDI A Journal of World Insect Systematics 0506 Annotated checklist and biogeographic composition of the Lycaenidae (Lepidoptera) of Trinidad, West Indies Matthew J.W. Cock CABI, Bakeham Lane Egham, Surrey, TW20 9TY United Kingdom Robert K. Robbins Smithsonian Institution PO Box 37012, NHB Stop 105 (E-514) Washington, DC 20013-7012 USA Date of Issue: October 21, 2016 CENTER FOR SYSTEMATIC ENTOMOLOGY, INC., Gainesville, FL Matthew J.W. Cock and Robert K. Robbins Annotated checklist and biogeographic composition of the Lycaenidae (Lepidoptera) of Trinidad, West Indies Insecta Mundi 0506: 1–33 ZooBank Registered: urn:lsid:zoobank.org:pub:37A7668A-0D83-4DB0-BD28-C36302F18398 Published in 2016 by Center for Systematic Entomology, Inc. P. O. Box 141874 Gainesville, FL 32614-1874 USA http://centerforsystematicentomology.org/ Insecta Mundi is a journal primarily devoted to insect systematics, but articles can be published on any non-marine arthropod. Topics considered for publication include systematics, taxonomy, nomenclature, checklists, faunal works, and natural history. Insecta Mundi will not consider works in the applied sciences (i.e. medical entomology, pest control research, etc.), and no longer publishes book reviews or editorials. Insecta Mundi publishes original research or discoveries in an inexpensive and timely manner, distributing them free via open access on the internet on the date of publication. Insecta Mundi is referenced or abstracted by several sources including the Zoological Record, CAB Ab- stracts, etc. Insecta Mundi is published irregularly throughout the year, with completed manuscripts assigned an individual number. Manuscripts must be peer reviewed prior to submission, after which they are reviewed by the editorial board to ensure quality. -
Food Quality, Competition, and Parasitism Influence Feeding Preference in a Neotropical Lepidopteran
Ecology, 87(12), 2006, pp. 3058–3069 Ó 2006 by the Ecological Society of America FOOD QUALITY, COMPETITION, AND PARASITISM INFLUENCE FEEDING PREFERENCE IN A NEOTROPICAL LEPIDOPTERAN 1,2,3 2 2 1,2 THOMAS A. KURSAR, BRETT T. WOLFE, MARY JANE EPPS, AND PHYLLIS D. COLEY 1Department of Biology, University of Utah, Salt Lake City, Utah 84112 USA 2Smithsonian Tropical Research Institute, Balboa, Panama Abstract. We surveyed Lepidoptera found on 11 species of Inga (Fabaceae:Mimosoideae) co-existing on Barro Colorado Island, Panama, to evaluate factors influencing diet choice. Of the 47 species of caterpillars (747 individuals) recorded, each fed on a distinct set of Inga.In the field, 96% of the individuals were found on young leaves. Growth rates of caterpillars that were fed leaves in the laboratory were 60% higher on young leaves compared to mature leaves. When caterpillars were fed leaves of nonhost Inga, they grew more slowly. These data provide support for a link between preference and performance. However, among hosts on which larvae normally occurred, faster growth rates were not associated with greater host electivity (the proportion of larvae found on each host species in the field, corrected for host abundance). Growth rates on normal hosts were positively correlated with leaf expansion rates of the host, and fast expansion was associated with leaves with higher nutritional content. Detailed studies on a gelechiid leaf roller, the species with the largest diet breadth, allowed us to assess the importance of factors other than growth that could influence diet electivity. This species showed a 1.7-fold difference in growth rate among Inga hosts and faster growth on species with fast-expanding leaves. -
Five New Riodinid Species from the Napo Region of Ecuador and Peru (Lepidoptera: Riodinidae)
Vol. 12 No. 1-2 2001 HALL and HARVEY: New Riodinids from Ecuador and Peru 35 TROPICAL LEPIDOPTERA, 12(1-2): 35-41 (2004) FIVE NEW RIODINID SPECIES FROM THE NAPO REGION OF ECUADOR AND PERU (LEPIDOPTERA: RIODINIDAE) JASON P. W. HALL AND DONALD J. HARVEY Dept. of Systematic Biology-Entomology, National Museum of Natural History, Smithsonian Institution, Washington. DC 20560-0127, USA ABSTRACT.- Five new riodinid species in the genera Euselasia Hu'bner, [1819] (Euselasia michaeli n. sp. and Euselasia rufomarginata n. sp.), Mesosemia Hiibner, [1819] (Mesosemia kahuapayani n. sp. and Mesosemia quadralineata n. sp.), and Calospila Geyer, [1832] (Calospila napoensis n. sp.), are described from the Napo river region of Ecuador and northern Peru. We make the following nomenclatural changes: Mesosemia materna Stichel, 1909, and M. subtilis Stichel, 1909 = M. thymetus umbrosa Stichel, 1909 (n. syns.), M. sylvina Bates, 1868 = M. cippus Hewitson, 1859 (n. syn.), Calospila cerealis (Hewitson, 1863) = C. rhesa (Hewitson, 1858) (n. syn.), and C. pirene (Godman, 1903) and C. caecina (C. & R. Felder, 1865) are reinstated to species status (stat. revs.). KEY WORDS: bioinventory, Bolivia, Brazil, Calospila napoensis n. sp., Colombia, Ecuador, Euselasia michaeli n. sp., Euselasia rufomarginata n. sp., Mesosemia kahuapayani n. sp., Mesosemia quadralineata n. sp., Neotropical, South America, taxonomy. The upper Amazon basin is well known to be the center of Euselasia rufomarginata Hall & Harvey, new sp. riodinid butterfly diversity (Robbins et al., 1996; Robbins & Opler, Fig. la,b; 6a,b 1997), but to date detailed results of long-term bioinventory work have only been reported for southwestern Brazil and southern Peru Description.- MALE: forewing length 18mm.