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Molecular Phylogeny, Divergence Times and Biogeography of Spiders of the Subfamily Euophryinae (Araneae: Salticidae) ⇑ Jun-Xia Zhang A, , Wayne P
Molecular Phylogenetics and Evolution 68 (2013) 81–92 Contents lists available at SciVerse ScienceDirect Molec ular Phylo genetics and Evolution journal homepage: www.elsevier.com/locate/ympev Molecular phylogeny, divergence times and biogeography of spiders of the subfamily Euophryinae (Araneae: Salticidae) ⇑ Jun-Xia Zhang a, , Wayne P. Maddison a,b a Department of Zoology, University of British Columbia, Vancouver, BC, Canada V6T 1Z4 b Department of Botany and Beaty Biodiversity Museum, University of British Columbia, Vancouver, BC, Canada V6T 1Z4 article info abstract Article history: We investigate phylogenetic relationships of the jumping spider subfamily Euophryinae, diverse in spe- Received 10 August 2012 cies and genera in both the Old World and New World. DNA sequence data of four gene regions (nuclear: Revised 17 February 2013 28S, Actin 5C; mitochondrial: 16S-ND1, COI) were collected from 263 jumping spider species. The molec- Accepted 13 March 2013 ular phylogeny obtained by Bayesian, likelihood and parsimony methods strongly supports the mono- Available online 28 March 2013 phyly of a Euophryinae re-delimited to include 85 genera. Diolenius and its relatives are shown to be euophryines. Euophryines from different continental regions generally form separate clades on the phy- Keywords: logeny, with few cases of mixture. Known fossils of jumping spiders were used to calibrate a divergence Phylogeny time analysis, which suggests most divergences of euophryines were after the Eocene. Given the diver- Temporal divergence Biogeography gence times, several intercontinental dispersal event sare required to explain the distribution of euophry- Intercontinental dispersal ines. Early transitions of continental distribution between the Old and New World may have been Euophryinae facilitated by the Antarctic land bridge, which euophryines may have been uniquely able to exploit Diolenius because of their apparent cold tolerance. -
Hemiptera: Heteroptera: Reduviidae) of Uruguay: a Synoptic Catalogue As a Contribution to the Study of Austral Biodiversity
Zootaxa 3006: 50–62 (2011) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2011 · Magnolia Press ISSN 1175-5334 (online edition) Assassin bugs (Hemiptera: Heteroptera: Reduviidae) of Uruguay: A synoptic catalogue as a contribution to the study of Austral biodiversity MARTIN-PARK, ABDIEL1 & COSCARÓN, MARIA DEL CARMEN2 1 Universidad Autónoma de Yucatán – Campus Ciencias Biológicas y Agropecuarias – Fac. de Medicina Veterinaria y Zootecnia A.P. 4-116 Col. Itzimná, 97100. Mérida, Yucatán, México. E-mail: [email protected] 2 Museo de La Plata, Div. Entomología, Paseo del Bosque, 1900 La Plata, Argentina. E-mail: [email protected] Abstract The first synoptic catalogue of Reduviidae is given to Uruguay including nine subfamilies, Ectrichodiinae (4), Emesinae (1), Hammacerinae (1), Harpactorinae (11), Peiratinae (4), Phymatinae (3), Reduviinae (5), Stenopodainae (7), Triatominae (9), being Harpactorinae and Triatominae the best represented by eleven and nine species respectively. Criceptopareis tucumana (Berg) is mentioned for the first time for Uruguay and is confirmed the distribution for Atrachelus cinereus (Fabricius), Melanolestes argentinus Berg, Rasahus hamatus (Fabricius), Zelurus femoralis femoralis (Stål), Diaditus semicolon Stål, Triatoma infestans (Klug) and Triatoma rubrovaria (Blanchard) from the material belonging to the Museo de La Plata (Argentina). This information is of valuable for insect’s conservation biodiversity programs. Keywords: Reduviidae, Heteroptera, Uruguay, Synonymies, Distribution Introduction Reduviidae is one of the five largest families of Heteroptera, comprising about 981 genera and more than 6878 spe- cies, with most occurring in the tropics (Henry 2009). Reduviids take place in all biogeographical regions (Schuh & Slater 1995). They are voracious predators of insects and arthropods (Ambrose 2006); nevertheless some like Triatominae species are hematophagous and important vector of Chagas Disease (Coscarón 2002). -
Introducción General 1
UNIVERSIDAD DE BUENOS AIRES Facultad de Ciencias Exactas y Naturales Estudio de la diversidad de insectos asociados a las principales plagas de Eucalyptus spp., para la selección de potenciales agentes de control biológico Tesis presentada para optar al título de Doctora de la Universidad de Buenos Aires en el área Ciencias Biológicas. Eliana Marina Cuello Directores de Tesis: Dra. Silvia N. López Dr. Eduardo N. Botto Consejera de Estudios: Dra. María Busch Lugar de trabajo: Insectario de Investigaciones para la Lucha Biológica, Instituto de Microbiología y Zoología Agrícola, INTA, Castelar. Fecha de defensa: 15 de marzo de 2019 1 Estudio de la diversidad de insectos asociados a las plagas principales de Eucalyptus spp., para la selección de potenciales agentes de control biológico Resumen Las plagas de eucaliptos más importantes en la Argentina son Glycaspis brimblecombei, Thaumastocoris peregrinus y Leptocybe invasa, todas ellas de reciente aparición en nuestro país. El abordaje más efectivo al problema de las plagas forestales es el manejo integrado, que combina diferentes tácticas entre las que se incluye el control biológico. El objetivo de esta tesis fue estudiar la diversidad de insectos asociados a Eucalyptus spp., con énfasis en las asociaciones tróficas que vinculan a G. brimblecombei y T. peregrinus con sus enemigos naturales (parasitoides/predadores), con el fin de identificar potenciales agentes para su control biológico. Se investigaron las variaciones en la abundancia de G. brimblecombei, T. peregrinus y L. invasa y la influencia de las variables meteorológicas en diferentes especies de eucaliptos. Se analizó la diversidad de insectos entomófagos y sus interacciones con G. brimblecombei y T. -
The Beetle Fauna of Dominica, Lesser Antilles (Insecta: Coleoptera): Diversity and Distribution
INSECTA MUNDI, Vol. 20, No. 3-4, September-December, 2006 165 The beetle fauna of Dominica, Lesser Antilles (Insecta: Coleoptera): Diversity and distribution Stewart B. Peck Department of Biology, Carleton University, 1125 Colonel By Drive, Ottawa, Ontario K1S 5B6, Canada stewart_peck@carleton. ca Abstract. The beetle fauna of the island of Dominica is summarized. It is presently known to contain 269 genera, and 361 species (in 42 families), of which 347 are named at a species level. Of these, 62 species are endemic to the island. The other naturally occurring species number 262, and another 23 species are of such wide distribution that they have probably been accidentally introduced and distributed, at least in part, by human activities. Undoubtedly, the actual numbers of species on Dominica are many times higher than now reported. This highlights the poor level of knowledge of the beetles of Dominica and the Lesser Antilles in general. Of the species known to occur elsewhere, the largest numbers are shared with neighboring Guadeloupe (201), and then with South America (126), Puerto Rico (113), Cuba (107), and Mexico-Central America (108). The Antillean island chain probably represents the main avenue of natural overwater dispersal via intermediate stepping-stone islands. The distributional patterns of the species shared with Dominica and elsewhere in the Caribbean suggest stages in a dynamic taxon cycle of species origin, range expansion, distribution contraction, and re-speciation. Introduction windward (eastern) side (with an average of 250 mm of rain annually). Rainfall is heavy and varies season- The islands of the West Indies are increasingly ally, with the dry season from mid-January to mid- recognized as a hotspot for species biodiversity June and the rainy season from mid-June to mid- (Myers et al. -
Annotated Checklist of the Butterflies of Bentsen-Rio Grande Valley State
AN ANNOTATED CHECKLIST OF THE BUTTERFLIES (LEPIDOPTERA: RHOPALOCERA) OF BENTSEN-RIO GRANDE STATE VALLEY PARK AND VICINITY JUNE, 1974 Published by TEXAS PARKS & WILDLIFE DEPARTMENT BENTSEN-RIO GRANDE VALLEY STATE PARK P.O. 30X 988; MISSION, TEXAS 78572 INTRODUCTION The species listed here in are primarily a result of the collecting by the authors during the period 1972-1973. Certain important records of the previous several years are also included. Additionally, the checklist incorporates records of a number of other lepidopterists. The primary focus of the checklist, then, is upon recent collecting, rather than being an attempt to list all known records from the Mid-Valley area. All lepidopterists collecting in the park and vicinity are urged to send copies of their records to the authors and/or the park authorities. A number of species on the list have been taken in Hidalgo Co. but not yet within the actual confines of the park; the annotations will indicate which species these are. Some of these have been taken at Santa Ana National Wildlife Refuge, approximately thirty miles down river, in habitats similar to those within the park. Others have been taken within several miles of the park, in nearby towns and along roadsides. These species can be reasonably expected to occur in the park, and their inclusion upon this list should alert the collector to their possible presence. The annotations have been kept necessarily brief. They are intended to aid the visiting lepidopterist in evaluating the significance of his catches. Local larval food plants are given where known. Much, however, is still to be learned regarding the life histories of even some of the commoner species. -
Phylogeny and Biogeography of Hawkmoths (Lepidoptera: Sphingidae): Evidence from Five Nuclear Genes
Phylogeny and Biogeography of Hawkmoths (Lepidoptera: Sphingidae): Evidence from Five Nuclear Genes Akito Y. Kawahara1*, Andre A. Mignault1, Jerome C. Regier2, Ian J. Kitching3, Charles Mitter1 1 Department of Entomology, College Park, Maryland, United States of America, 2 Center for Biosystems Research, University of Maryland Biotechnology Institute, College Park, Maryland, United States of America, 3 Department of Entomology, The Natural History Museum, London, United Kingdom Abstract Background: The 1400 species of hawkmoths (Lepidoptera: Sphingidae) comprise one of most conspicuous and well- studied groups of insects, and provide model systems for diverse biological disciplines. However, a robust phylogenetic framework for the family is currently lacking. Morphology is unable to confidently determine relationships among most groups. As a major step toward understanding relationships of this model group, we have undertaken the first large-scale molecular phylogenetic analysis of hawkmoths representing all subfamilies, tribes and subtribes. Methodology/Principal Findings: The data set consisted of 131 sphingid species and 6793 bp of sequence from five protein-coding nuclear genes. Maximum likelihood and parsimony analyses provided strong support for more than two- thirds of all nodes, including strong signal for or against nearly all of the fifteen current subfamily, tribal and sub-tribal groupings. Monophyly was strongly supported for some of these, including Macroglossinae, Sphinginae, Acherontiini, Ambulycini, Philampelini, Choerocampina, and Hemarina. Other groupings proved para- or polyphyletic, and will need significant redefinition; these include Smerinthinae, Smerinthini, Sphingini, Sphingulini, Dilophonotini, Dilophonotina, Macroglossini, and Macroglossina. The basal divergence, strongly supported, is between Macroglossinae and Smerinthinae+Sphinginae. All genes contribute significantly to the signal from the combined data set, and there is little conflict between genes. -
Lista Taxonómica Actualizada De Los Esfíngidos De Cuba (Lepidoptera)
Lista taxonómica actualizada de los esfíngidos de Cuba (Lepidoptera) Alfonso Iorio [email protected] La última y más reciente clasificacion taxonómica (la misma que adopté en mi libro sobre los esfíngidos de Ecuador: “Mariposas del Ecuador. Sphingidae”) es de Kitching & Cadiou (2000). Así, la familia contiene las siguentes agrupaciones: Familia: Sphingidae Latreille, [1802] Subfamilia: Smerinthinae Grote & Robinson, 1865 Tribu: Smerinthini Grote & Robinson, 1865 Sphingulini Rothschild & Jordan, 1903 Ambulycini Butler, 1876 Subfamilia: Sphinginae Latreille, [1802] Tribu: Sphingini Latreille, [1802] Acherontiini Boisduval, [1875] Subfamilia: Macroglossinae Harris, 1839 Tribu: Dilophonotini Burmeister, 1878 Subtribu: Dilophonotina Burmeister, 1878 Hemarina Tutt, 1902 Tribu : Philampelini Burmeister, 1878 Macroglossini Harris, 1839 Subtribu: Macroglossina Harris, 1839 Choerocampina Grote & Robinson, 1865 Subfamilias, tribus y subtribus que se encuentran en Cuba: Familia: Sphingidae Latreille, [1802] Subfamilia: Smerinthinae Grote & Robinson, 1865 Tribu: Ambulycini Butler, 1876 Protambulyx strigilis (L., 1771) Adhemarius gannascus cubanus (Rothschild & Jordan, 1908) Subfamilia: Sphinginae Latreille, [1802] Tribu: Sphingini Latreille, [1802] Nannoparce poeyi (Grote, 1865) Manduca afflicta (Grote, 1865) Manduca brontes cubensis (Grote, 1865) Manduca quinquemaculatus (Haworth, 1803) Manduca rustica cubana (Wood, 1915) Manduca sexta jamaicensis (Butler, 1875) Neococytius cluentius (Cramer, 1775) Cocytius antaeus (Drury, 1773) Cocytius duponchel -
70.1, 5 September 2008 ISSN 1944-8120
PECKHAMIA 70.1, 5 September 2008 ISSN 1944-8120 This is a PDF version of PECKHAMIA 3(2): 27-60, December 1995. Pagination of the original document has been retained. PECKHAMIA Volume 3 Number 2 Publication of the Peckham Society, an informal organization dedicated to research in the biology of jumping spiders. CONTENTS ARTICLES: A LIST OF THE JUMPING SPIDERS (SALTICIDAE) OF THE ISLANDS OF THE CARIBBEAN REGION G. B. Edwards and Robert J. Wolff..........................................................................27 DECEMBER 1995 A LIST OF THE JUMPING SPIDERS (SALTICIDAE) OF THE ISLANDS OF THE CARIBBEAN REGION G. B. Edwards Florida State Collection of Arthropods Division of Plant Industry P. O. Box 147100 Gainesville, FL 32614-7100 USA Robert J. Wolff1 Biology Department Trinity Christian College 6601 West College Drive Palos Heights, IL 60463 USA The following is a list of the jumping spiders that have been reported from the Caribbean region. We have interpreted this in a broad sense, so that all islands from Trinidad to the Bahamas have been included. Furthermore, we have included Bermuda, even though it is well north of the Caribbean region proper, as a more logical extension of the island fauna rather than the continental North American fauna. This was mentioned by Banks (1902b) nearly a century ago. Country or region (e. g., pantropical) records are included for those species which have broader ranges than the Caribbean area. We have not specifically included the islands of the Florida Keys, even though these could legitimately be included in the Caribbean region, because the known fauna is mostly continental. However, when Florida is known as the only continental U.S.A. -
2018 Bibliography of Taxonomic Literature
Bibliography of taxonomic literature for marine and brackish water Fauna and Flora of the North East Atlantic. Compiled by: Tim Worsfold Reviewed by: David Hall, NMBAQCS Project Manager Edited by: Myles O'Reilly, Contract Manager, SEPA Contact: [email protected] APEM Ltd. Date of Issue: February 2018 Bibliography of taxonomic literature 2017/18 (Year 24) 1. Introduction 3 1.1 References for introduction 5 2. Identification literature for benthic invertebrates (by taxonomic group) 5 2.1 General 5 2.2 Protozoa 7 2.3 Porifera 7 2.4 Cnidaria 8 2.5 Entoprocta 13 2.6 Platyhelminthes 13 2.7 Gnathostomulida 16 2.8 Nemertea 16 2.9 Rotifera 17 2.10 Gastrotricha 18 2.11 Nematoda 18 2.12 Kinorhyncha 19 2.13 Loricifera 20 2.14 Echiura 20 2.15 Sipuncula 20 2.16 Priapulida 21 2.17 Annelida 22 2.18 Arthropoda 76 2.19 Tardigrada 117 2.20 Mollusca 118 2.21 Brachiopoda 141 2.22 Cycliophora 141 2.23 Phoronida 141 2.24 Bryozoa 141 2.25 Chaetognatha 144 2.26 Echinodermata 144 2.27 Hemichordata 146 2.28 Chordata 146 3. Identification literature for fish 148 4. Identification literature for marine zooplankton 151 4.1 General 151 4.2 Protozoa 152 NMBAQC Scheme – Bibliography of taxonomic literature 2 4.3 Cnidaria 153 4.4 Ctenophora 156 4.5 Nemertea 156 4.6 Rotifera 156 4.7 Annelida 157 4.8 Arthropoda 157 4.9 Mollusca 167 4.10 Phoronida 169 4.11 Bryozoa 169 4.12 Chaetognatha 169 4.13 Echinodermata 169 4.14 Hemichordata 169 4.15 Chordata 169 5. -
BUTTERFLIES in Thewest Indies of the Caribbean
PO Box 9021, Wilmington, DE 19809, USA E-mail: [email protected]@focusonnature.com Phone: Toll-free in USA 1-888-721-3555 oror 302/529-1876302/529-1876 BUTTERFLIES and MOTHS in the West Indies of the Caribbean in Antigua and Barbuda the Bahamas Barbados the Cayman Islands Cuba Dominica the Dominican Republic Guadeloupe Jamaica Montserrat Puerto Rico Saint Lucia Saint Vincent the Virgin Islands and the ABC islands of Aruba, Bonaire, and Curacao Butterflies in the Caribbean exclusively in Trinidad & Tobago are not in this list. Focus On Nature Tours in the Caribbean have been in: January, February, March, April, May, July, and December. Upper right photo: a HISPANIOLAN KING, Anetia jaegeri, photographed during the FONT tour in the Dominican Republic in February 2012. The genus is nearly entirely in West Indian islands, the species is nearly restricted to Hispaniola. This list of Butterflies of the West Indies compiled by Armas Hill Among the butterfly groupings in this list, links to: Swallowtails: family PAPILIONIDAE with the genera: Battus, Papilio, Parides Whites, Yellows, Sulphurs: family PIERIDAE Mimic-whites: subfamily DISMORPHIINAE with the genus: Dismorphia Subfamily PIERINAE withwith thethe genera:genera: Ascia,Ascia, Ganyra,Ganyra, Glutophrissa,Glutophrissa, MeleteMelete Subfamily COLIADINAE with the genera: Abaeis, Anteos, Aphrissa, Eurema, Kricogonia, Nathalis, Phoebis, Pyrisitia, Zerene Gossamer Wings: family LYCAENIDAE Hairstreaks: subfamily THECLINAE with the genera: Allosmaitia, Calycopis, Chlorostrymon, Cyanophrys, -
Free-Living Marine Nematodes from San Antonio Bay (Río Negro, Argentina)
A peer-reviewed open-access journal ZooKeys 574: 43–55Free-living (2016) marine nematodes from San Antonio Bay (Río Negro, Argentina) 43 doi: 10.3897/zookeys.574.7222 DATA PAPER http://zookeys.pensoft.net Launched to accelerate biodiversity research Free-living marine nematodes from San Antonio Bay (Río Negro, Argentina) Gabriela Villares1, Virginia Lo Russo1, Catalina Pastor de Ward1, Viviana Milano2, Lidia Miyashiro3, Renato Mazzanti3 1 Laboratorio de Meiobentos LAMEIMA-CENPAT-CONICET, Boulevard Brown 2915, U9120ACF, Puerto Madryn, Argentina 2 Universidad Nacional de la Patagonia San Juan Bosco, sede Puerto Madryn. Boulevard Brown 3051, U9120ACF, Puerto Madryn, Argentina 3Centro de Cómputos CENPAT-CONICET, Boulevard Brown 2915, U9120ACF, Puerto Madryn, Argentina Corresponding author: Gabriela Villares ([email protected]) Academic editor: H-P Fagerholm | Received 18 November 2015 | Accepted 11 February 2016 | Published 28 March 2016 http://zoobank.org/3E8B6DD5-51FA-499D-AA94-6D426D5B1913 Citation: Villares G, Lo Russo V, Pastor de Ward C, Milano V, Miyashiro L, Mazzanti R (2016) Free-living marine nematodes from San Antonio Bay (Río Negro, Argentina). ZooKeys 574: 43–55. doi: 10.3897/zookeys.574.7222 Abstract The dataset of free-living marine nematodes of San Antonio Bay is based on sediment samples collected in February 2009 during doctoral theses funded by CONICET grants. A total of 36 samples has been taken at three locations in the San Antonio Bay, Santa Cruz Province, Argentina on the coastal littoral at three tidal levels. This presents a unique and important collection for benthic biodiversity assessment of Patagonian nematodes as this area remains one of the least known regions. -
Florida Keys Species List
FKNMS Species List A B C D E F G H I J K L M N O P Q R S T 1 Marine and Terrestrial Species of the Florida Keys 2 Phylum Subphylum Class Subclass Order Suborder Infraorder Superfamily Family Scientific Name Common Name Notes 3 1 Porifera (Sponges) Demospongia Dictyoceratida Spongiidae Euryspongia rosea species from G.P. Schmahl, BNP survey 4 2 Fasciospongia cerebriformis species from G.P. Schmahl, BNP survey 5 3 Hippospongia gossypina Velvet sponge 6 4 Hippospongia lachne Sheepswool sponge 7 5 Oligoceras violacea Tortugas survey, Wheaton list 8 6 Spongia barbara Yellow sponge 9 7 Spongia graminea Glove sponge 10 8 Spongia obscura Grass sponge 11 9 Spongia sterea Wire sponge 12 10 Irciniidae Ircinia campana Vase sponge 13 11 Ircinia felix Stinker sponge 14 12 Ircinia cf. Ramosa species from G.P. Schmahl, BNP survey 15 13 Ircinia strobilina Black-ball sponge 16 14 Smenospongia aurea species from G.P. Schmahl, BNP survey, Tortugas survey, Wheaton list 17 15 Thorecta horridus recorded from Keys by Wiedenmayer 18 16 Dendroceratida Dysideidae Dysidea etheria species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 19 17 Dysidea fragilis species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 20 18 Dysidea janiae species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 21 19 Dysidea variabilis species from G.P. Schmahl, BNP survey 22 20 Verongida Druinellidae Pseudoceratina crassa Branching tube sponge 23 21 Aplysinidae Aplysina archeri species from G.P. Schmahl, BNP survey 24 22 Aplysina cauliformis Row pore rope sponge 25 23 Aplysina fistularis Yellow tube sponge 26 24 Aplysina lacunosa 27 25 Verongula rigida Pitted sponge 28 26 Darwinellidae Aplysilla sulfurea species from G.P.